Science.gov

Sample records for 100-nr-2 apatite treatability

  1. 100-NR-2 Apatite Treatability Test: Fall 2010 Tracer Infiltration Test (White Paper)

    SciTech Connect

    Vermeul, Vincent R.; Fritz, Brad G.; Fruchter, Jonathan S.; Greenwood, William J.; Johnson, Timothy C.; Horner, Jacob A.; Strickland, Christopher E.; Szecsody, James E.; Williams, Mark D.

    2011-04-14

    change and the associated change in moisture content so that 4D images of moisture content change can be generated. Results from this field test will be available for any future Ca-citrate-PO4 amendment infiltration tests, which would be designed to evaluate the efficacy of using near surface application of amendments to form apatite mineral phases in the upper portion of the zone of water table fluctuation.

  2. 100-NR-2 Apatite Treatability Test: High-Concentration Calcium-Citrate-Phosphate Solution Injection for In Situ Strontium-90 Immobilization

    SciTech Connect

    Vermeul, Vincent R.; Fritz, Brad G.; Fruchter, Jonathan S.; Szecsody, James E.; Williams, Mark D.

    2010-09-01

    Following an evaluation of potential strontium-90 (90Sr) treatment technologies and their applicability under 100-NR-2 hydrogeologic conditions, the U.S. Department of Energy (DOE), Fluor Hanford, Inc. (now CH2M Hill Plateau Remediation Company [CHPRC]), Pacific Northwest National Laboratory, and the Washington State Department of Ecology agreed that the long-term strategy for groundwater remediation at the 100-N Area should include apatite as the primary treatment technology. This agreement was based on results from an evaluation of remedial alternatives that identified the apatite permeable reactive barrier (PRB) technology as the approach showing the greatest promise for reducing 90Sr flux to the Columbia River at a reasonable cost. This letter report documents work completed to date on development of a high-concentration amendment formulation and initial field-scale testing of this amendment solution.

  3. Interim Report: 100-NR-2 Apatite Treatability Test: Low Concentration Calcium Citrate-Phosphate Solution Injection for In Situ Strontium-90 Immobilization

    SciTech Connect

    Williams, Mark D.; Fritz, Brad G.; Mendoza, Donaldo P.; Rockhold, Mark L.; Thorne, Paul D.; Xie, YuLong; Bjornstad, Bruce N.; Mackley, Rob D.; Newcomer, Darrell R.; Szecsody, James E.; Vermeul, Vincent R.

    2008-07-11

    Following an evaluation of potential Sr-90 treatment technologies and their applicability under 100-NR-2 hydrogeologic conditions, U.S. Department of Energy, Fluor Hanford, Inc., Pacific Northwest National Laboratory, and the Washington Department of Ecology agreed that the long-term strategy for groundwater remediation at 100-N Area will include apatite sequestration as the primary treatment, followed by a secondary treatment if necessary (most likely phytoremediation). Since then, the agencies have worked together to agree on which apatite sequestration technology has the greatest chance of reducing Sr-90 flux to the river at a reasonable cost. In July 2005, aqueous injection, (i.e., the introduction of apatite-forming chemicals into the subsurface) was endorsed as the interim remedy and selected for field testing. Studies are in progress to assess the efficacy of in situ apatite formation by aqueous solution injection to address both the vadose zone and the shallow aquifer along the 300 ft of shoreline where Sr-90 concentrations are highest. This report describes the field testing of the shallow aquifer treatment.

  4. Pacific Northwest National Laboratory Apatite Investigation at the 100-NR-2 Quality Assurance Project Plan

    SciTech Connect

    Fix, N. J.

    2008-03-28

    This Quality Assurance Project Plan provides the quality assurance requirements and processes that will be followed by staff working on the 100-NR-2 Apatite Project. The U.S. Department of Energy, Fluor Hanford, Inc., Pacific Northwest National Laboratory, and the Washington Department of Ecology agreed that the long-term strategy for groundwater remediation at 100-N would include apatite sequestration as the primary treatment, followed by a secondary treatment. The scope of this project covers the technical support needed before, during, and after treatment of the targeted subsurface environment using a new high-concentration formulation.

  5. PNNL Apatite Investigation at 100-NR-2 Quality Assurance Project Plan

    SciTech Connect

    Fix, N. J.

    2009-04-02

    In 2004, the U.S. Department of Energy, Fluor Hanford, Inc., Pacific Northwest National Laboratory (PNNL), and the Washington Department of Ecology agreed that the long-term strategy for groundwater remediation at the 100-N Area would include apatite sequestration as the primary treatment, followed by a secondary treatment if necessary. Since then, the agencies have worked together to agree on which apatite sequestration technology has the greatest chance of reducing strontium-90 flux to the Columbia River. This Quality Assurance Project Plan provides the quality assurance requirements and processes that will be followed by staff working on the PNNL Apatite Investigation at 100-NR-2 Project. The plan is designed to be used exclusively by project staff.

  6. FIELD TEST INSTRUCTION 100-NR-2 OPERABLE UNIT DESIGN OPTIMIZATION STUDY FOR SEQUESTRATION OF SR-90 SATURATED ZONE APATITE PERMEABLE REACTIVE BARRIER EXTENSION

    SciTech Connect

    BOWLES NA

    2010-10-06

    The objective of this field test instruction is to provide technical guidance for aqueous injection emplacement of an extension apatite permeable reactive barrier (PRE) for the sequestration of strontium-90 (Sr-90) using a high concentration amendment formulation. These field activities will be conducted according to the guidelines established in DOE/RL-2010-29, 100-NR-2 Design Optimization Study, hereafter referred to as the DOS. The DOS supports the Federal Facility Agreement Consent Order (EPA et al., 1989), Milestone M-16-06-01, and 'Complete Construction of a Permeable Reactive Barrier at 100-N.' Injections of apatite precursor chemicals will occur at an equal distance intervals on each end of the existing PRE to extend the PRB from the existing 91 m (300 ft) to at least 274 m (900 ft). Field testing at the 100-N Area Apatite Treatability Test Site, as depicted on Figure 1, shows that the barrier is categorized by two general hydrologic conceptual models based on overall well capacity and contrast between the Hanford and Ringold hydraulic conductivities. The upstream portion of the original barrier, shown on Figure 1, is characterized by relatively low overall well specific capacity. This is estimated from well development data and a lower contrast in hydraulic conductivity between the Hanford formation and Ringold Formations. Comparison of test results from these two locations indicate that permeability contrast between the Hanford formation and Ringold Formation is significantly less over the upstream one-third of the barrier. The estimated hydraulic conductivity for the Hanford formation and Ringold Formation over the upstream portion of the barrier based on observations during emplacement of the existing 91 m (300 ft) PRB is approximately 12 and 10 m/day (39 and 32 ft/day), respectively (PNNL-17429). However, these estimates should be used as a rough guideline only, as significant variability in hydraulic conductivity is likely to be observed in the

  7. 100-NR-2 Apatite Treatability Test: An update on Barrier Performance

    SciTech Connect

    Fritz, Brad G.; Vermeul, Vincent R.; Fruchter, Jonathan S.; Szecsody, James E.; Williams, Mark D.

    2011-05-01

    This report updates a previous report covering the performance of a permeable reactive barrier installed at 100N. In this report we re-evaluate the results after having an additional year of performance monitoring data to incorporate.

  8. Hanford Apatite Treatability Test Report Errata: Apatite Mass Loading Calculation

    SciTech Connect

    Szecsody, James E.; Vermeul, Vincent R.; Williams, Mark D.; Truex, Michael J.

    2014-05-19

    The objective of this errata report is to document an error in the apatite loading (i.e., treatment capacity) estimate reported in previous apatite treatability test reports and provide additional calculation details for estimating apatite loading and barrier longevity. The apatite treatability test final report (PNNL-19572; Vermeul et al. 2010) documents the results of the first field-scale evaluation of the injectable apatite PRB technology. The apatite loading value in units of milligram-apatite per gram-sediment is incorrect in this and some other previous reports. The apatite loading in units of milligram phosphate per gram-sediment, however, is correct, and this is the unit used for comparison to field core sample measurements.

  9. Project Work Plan 100-N Area Strontium-90 Treatability Demonstration Project: Phytoremediation Along the 100-N Columbia River Riparian Zone

    SciTech Connect

    Ainsworth, Calvin C.

    2006-04-30

    The 100-N Area Innovative Treatment and Remediation Demonstration (ITRD) identified phyto¬remediation as a potential technology both for the removal of 90Sr from the soil of the riparian zone and as a filter for groundwater along the Columbia River. Recent greenhouse and growth chamber studies have demonstrated the viability of phytoextraction to remove 90Sr from this area’s soil/water; in conjunction with monitored natural attenuation and an apatite barrier the process would make an effective treatment for remediation of the 100-N Area 90Sr plume. All activities associated with the 100-NR-1 and 100-NR-2 Operable Units of the Hanford 100-N Area have had, and continue to have, significant regulatory and stakeholder participation. Beginning in 1998 with the ITRD process, presentations to the ITRD TAG were heavily attended by EPA, Washington State Department of Ecology, and stakeholders. In addition, three workshops have been held to receive regulatory and stakeholder feedback on monitored natural attenuation, the apatite barrier, and phytoremediation; these were held in Richland in August 2003, December 2004, and August 2005. The apatite injection treatability test plan (DOE 2005) describes phytoremediation as a technology to be evaluated during the March 2008 evaluation milestone as described in the Tri-Party Agreement change request (M-16-06-01 Change Control Form). If, during this evaluation milestone, phytoremediation is favorably evaluated it would be incorporated into the treatability test plan. The phytoremediation treatability test described in this proposal is strongly supported by the Washington State Department of Ecology.

  10. Annual Summary Report Calendar Year 2000 for the 100-HR-3, 100-KR-4, and 100-NR-2 Operable Units and Pump-and-Treat Operations

    SciTech Connect

    G. B. Mitchem

    2001-08-22

    This annual progress and performance evaluation report discusses the groundwater remedial actions in the 100 Area, including the interim actions at the 100-HR-3 and 100-KR-4 Operable Units, and also discusses the expedited response action in the 100-NR-2 operable unit.

  11. Treatable Dementias

    PubMed Central

    Mahler, Michael E.; Cummings, Jeffrey L.; Benson, D. Frank

    1987-01-01

    Dementia is an acquired impairment of intellect produced by brain dysfunction. In the past, dementia was regarded as inevitably chronic, progressive and irreversible. More recently dementia has been viewed as a clinical syndrome that may be produced by both irreversible and reversible conditions. Recognition of the presence of a dementia syndrome should be followed by an evaluation for potentially treatable causes of the intellectual deterioration. Dementia treatment includes therapy for reversible or curable dementias and nonspecific interventions that may improve the condition of patients with progressive dementia syndromes. PMID:3617715

  12. Polysomatic apatites.

    PubMed

    Baikie, Tom; Pramana, Stevin S; Ferraris, Cristiano; Huang, Yizhong; Kendrick, Emma; Knight, Kevin S; Ahmad, Zahara; White, T J

    2010-02-01

    Certain complex structures are logically regarded as intergrowths of chemically or topologically discrete modules. When the proportions of these components vary systematically a polysomatic series is created, whose construction provides a basis for understanding defects, symmetry alternation and trends in physical properties. Here, we describe the polysomatic family A(5N)B(3N)O(9N + 6)X(Ndelta) (2 < or = N < or = infinity) that is built by condensing N apatite modules (A(5)B(3)O(18)X(delta)) in configurations to create B(n)O(3n + 1) (1 < or = n < or = infinity) tetrahedral chains. Hydroxyapatite [Ca(10)(PO(4))(6)(OH)(2)] typifies a widely studied polysome where N = 2 and the tetrahedra are isolated in A(10)(BO(4))(6)X(2) compounds, but N = 3 A(15)(B(2)O(7))(3)(BO(4))(3)X(3) (ganomalite) and N = 4 A(20)(B(2)O(7))(6)X(4) (nasonite) are also known, with the X site untenanted or partially occupied as required for charge balance. The apatite modules, while topologically identical, are often compositionally or symmetrically distinct, and an infinite number of polysomes is feasible, generally with the restriction being that an A:B = 5:3 cation ratio be maintained. The end-members are the N = 2 polysome with all tetrahedra separated, and N = infinity, in which the hypothetical compound A(5)B(3)O(9)X contains infinite, corner-connected tetrahedral strings. The principal characteristics of a polysome are summarized using the nomenclature apatite-(A B X)-NS, where A/B/X are the most abundant species in these sites, N is the number of modules in the crystallographic repeat, and S is the symmetry symbol (usually H, T, M or A). This article examines the state-of-the-art in polysomatic apatite synthesis and crystallochemical design. It also presents X-ray and neutron powder diffraction investigations for several polysome chemical series and examines the prevalence of stacking disorder by electron microscopy. These insights into the structure-building principles of apatite

  13. TREATABILITY DATABASE DESCRIPTION

    EPA Science Inventory

    The Drinking Water Treatability Database (TDB) presents referenced information on the control of contaminants in drinking water. It allows drinking water utilities, first responders to spills or emergencies, treatment process designers, research organizations, academics, regulato...

  14. Soil washing treatability study

    SciTech Connect

    Krstich, M.

    1995-12-01

    Soil washing was identified as a viable treatment process option for remediating soil at the FEMP Environmental Management Project (FEMP). Little information relative to the specific application and potential effectiveness of the soil washing process exists that applies to the types of soil at the FEMP. To properly evaluate this process option in conjunction with the ongoing FEMP Remedial Investigation/Feasibility Study (RI/FS), a treatability testing program was necessary to provide a foundation for a detailed technical evaluation of the viability of the process. In August 1991, efforts were initiated to develop a work plan and experimental design for investigating the effectiveness of soil washing on FEMP soil. In August 1992, the final Treatability Study Work Plan for Operable Unit 5: Soil Washing (DOE 1992) was issued. This document shall be referenced throughout the remainder of this report as the Treatability Study Work Plan (TSWP). The purpose of this treatability study was to generate data to support initial screening and the detailed analysis of alternatives for the Operable Unit 5 FS.

  15. The lunar apatite paradox.

    PubMed

    Boyce, J W; Tomlinson, S M; McCubbin, F M; Greenwood, J P; Treiman, A H

    2014-04-25

    Recent discoveries of water-rich lunar apatite are more consistent with the hydrous magmas of Earth than the otherwise volatile-depleted rocks of the Moon. Paradoxically, this requires H-rich minerals to form in rocks that are otherwise nearly anhydrous. We modeled existing data from the literature, finding that nominally anhydrous minerals do not sufficiently fractionate H from F and Cl to generate H-rich apatite. Hydrous apatites are explained as the products of apatite-induced low magmatic fluorine, which increases the H/F ratio in melt and apatite. Mare basalts may contain hydrogen-rich apatite, but lunar magmas were most likely poor in hydrogen, in agreement with the volatile depletion that is both observed in lunar rocks and required for canonical giant-impact models of the formation of the Moon. PMID:24652938

  16. 100-N Area Strontium-90 Treatability Demonstration Project: Phytoextraction Along the 100-N Columbia River Riparian Zone – Field Treatability Study

    SciTech Connect

    Fellows, Robert J.; Fruchter, Jonathan S.; Driver, Crystal J.; Ainsworth, Calvin C.

    2010-01-11

    Strontium-90 (90Sr) is present both in the aquifer near the river and in the vadose and riparian zones of the river’s shore at 100-NR-2. Phytoextraction of 90Sr is being considered as a potential remediation system along the riparian zone of the Columbia River. Phytoextraction would employ coyote willow (Salix exigua). Past studies have shown that willow roots share uptake mechanisms for Sr with Ca, a plant macronutrient as well as no discrimination between Sr and 90Sr. Willow 90Sr concentration ratios [CR’s; (pCi 90Sr/g dry wt. of new growth tissue)/(pCi 90Sr/g soil porewater)] were consistently greater than 65 with three-quarters of the assimilated label partitioned into the above ground shoot. Insect herbivore experiments also demonstrated no significant potential for bioaccumulation or food chain transfer from their natural activities. The objectives of this field study were three-fold: (1) to demonstrate that a viable, “managed” plot of coyote willows can be established on the shoreline of the Columbia River that would survive the same microenvironment to be encountered at the 100-NR-2 shoreline; (2) to show through engineered barriers that large and small animal herbivores can be prevented from feeding on these plants; and (3) to show that once established, the plants will provide sufficient biomass annually to support the phytoextraction technology. A field treatability demonstration plot was established on the Columbia River shoreline alongside the 100-K West water intake at the end of January 2007. The plot was delimited by a 3.05 m high chain-link fence and was approximately 10 x 25 m in size. A layer of fine mesh metal small animal screening was placed around the plot at the base of the fencing to a depth of 45 cm. A total of sixty plants were placed in six slightly staggered rows with 1-m spacing between plants. The actual plot size was 0.00461 hectare (ha). At the time of planting (March 12, 2007), the plot was located about 10 m from the

  17. TREATABILITY MANUAL. VOLUME V: SUMMARY

    EPA Science Inventory

    The Treatability Manual presents in five volumes an extensive survey of the effectiveness of various water pollution treatment processes when applied to particular industrial effluents. This volume summarizes volumes one through four and outlines their potential utility to Nation...

  18. Interim Report: Uranium Stabilization Through Polyphosphate Injection - 300 Area Uranium Plume Treatability Demonstration Project

    SciTech Connect

    Wellman, Dawn M.; Pierce, Eric M.; Richards, Emily L.; Butler, Bart C.; Parker, Kent E.; Glovack, Julia N.; Burton, Sarah D.; Baum, Steven R.; Clayton, Eric T.; Rodriguez, Elsa A.

    2007-07-31

    This report presents results from bench-scale treatability studies conducted under site-specific conditions to optimize the polyphosphate amendment for implementation of a field-scale technology demonstration to treat aqueous uranium within the 300 Area aquifer of the Hanford site. The general treatability testing approach consists of conducting studies with site sediment and under site conditions, in order to develop an effective chemical formulation for the polyphosphate amendments and evaluate the transport properties of these amendments under site conditions. Phosphorus-31 (31P) NMR was utilized to determine the effects of Hanford groundwater and sediment on the degradation of inorganic phosphates. Static batch tests were conducted to optimize the composition of the polyphosphate formulation for the precipitation of apatite and autunite, as well as to quantify the kinetics, loading and stability of apatite as a long-term sorbent for uranium. Dynamic column tests were used to further optimize the polyphosphate formulation for emplacement within the subsurface and the formation of autunite and apatite. In addition, dynamic testing quantified the stability of autunite and apatite under relevant site conditions. Results of this investigation provide valuable information for designing a full-scale remediation of uranium in the 300 aquifer.

  19. TREATABILITY STUDIES FOR WOOD PRESERVING SITES

    EPA Science Inventory

    The U.S. Environmental Protection Agency (EPA), National Risk Management Research Laboratory (NRMRL), Site Management Support Branch, conducted a comprehensive treatability project for wood preserving sites in 1995 and 1996. This is a compilation report on the treatability studi...

  20. Challenges Associated with Apatite Remediation of Uranium in the 300 Area Aquifer

    SciTech Connect

    Wellman, Dawn M.; Fruchter, Jonathan S.; Vermeul, Vincent R.; Williams, Mark D.

    2008-05-01

    Sequestration of uranium as insoluble phosphate phases appears to be a promising alternative for treating the uranium-contaminated groundwater at the Hanford 300 Area. The proposed approach involves both the direct formation of autunite by the application of a polyphosphate mixture, as well as the formation of apatite in the aquifer as a continuing source of phosphate for long-term treatment of uranium. After a series of bench-scale tests, a field treatability test was conducted in a well at the 300 Area. The objective of the treatability test was to evaluate the efficacy of using polyphosphate injections to treat uranium-contaminated groundwater in situ. A test site consisting of an injection well and 15 monitoring wells was installed in the 300 Area near the process trenches that had previously received uranium-bearing effluents. The results indicated that while the direct formation of autunite appears to have been successful, the outcome of the apatite formation of the test was more limited. Two separate overarching issues impact the efficacy of apatite remediation for uranium sequestration within the 300 Area: 1) the efficacy of apatite for sequestering uranium under the present geochemical and hydrodynamic conditions, and 2) the formation and emplacement of apatite via polyphosphate technology. This paper summarizes these issues.

  1. Drinking Water Treatability Database (Database)

    EPA Science Inventory

    The drinking Water Treatability Database (TDB) will provide data taken from the literature on the control of contaminants in drinking water, and will be housed on an interactive, publicly-available USEPA web site. It can be used for identifying effective treatment processes, rec...

  2. Making chromosome abnormalities treatable conditions.

    PubMed

    Cody, Jannine DeMars; Hale, Daniel Esten

    2015-09-01

    Individuals affected by the classic chromosome deletion syndromes which were first identified at the beginning of the genetic age, are now positioned to benefit from genomic advances. This issue highlights five of these conditions (4p-, 5p-, 11q-, 18p-, and 18q-). It focuses on the increased in understanding of the molecular underpinnings and envisions how these can be transformed into effective treatments. While it is scientifically exciting to see the phenotypic manifestations of hemizygosity being increasingly understood at the molecular and cellular level, it is even more amazing to consider that we are now on the road to making chromosome abnormalities treatable conditions. PMID:26351122

  3. Treatability Test Plan for 300 Area Uranium Stabilization through Polyphosphate Injection

    SciTech Connect

    Vermeul, Vincent R.; Williams, Mark D.; Fritz, Brad G.; Mackley, Rob D.; Mendoza, Donaldo P.; Newcomer, Darrell R.; Rockhold, Mark L.; Williams, Bruce A.; Wellman, Dawn M.

    2007-06-01

    The U.S. Department of Energy has initiated a study into possible options for stabilizing uranium at the 300 Area using polyphosphate injection. As part of this effort, PNNL will perform bench- and field-scale treatability testing designed to evaluate the efficacy of using polyphosphate injections to reduced uranium concentrations in the groundwater to meet drinking water standards (30 ug/L) in situ. This technology works by forming phosphate minerals (autunite and apatite) in the aquifer that directly sequester the existing aqueous uranium in autunite minerals and precipitates apatite minerals for sorption and long term treatment of uranium migrating into the treatment zone, thus reducing current and future aqueous uranium concentrations. Polyphosphate injection was selected for testing based on technology screening as part of the 300-FF-5 Phase III Feasibility Study for treatment of uranium in the 300-Area.

  4. TREATABILITY MANUAL. VOLUME IV: COST ESTIMATING

    EPA Science Inventory

    The objective of the treatability program are: To provide readily accessible data and information on treatability of industrial and municipal waste streams for use by NPDES permit writers, enforcement personnel, and by industrial or municipal permit holders; To provide a basis fo...

  5. [How Treatable is Vascular Dementia?].

    PubMed

    Mori, Etsuro

    2016-04-01

    Vascular dementia is an umbrella term, encompassing the pathological changes in the brain due to cerebrovascular disease that result in dementia. Vascular dementia is the second most common form of dementia, after Alzheimer's disease. In this paper, I outline the concept of vascular dementia, the key aspects of the disease that are yet to be clarified, and the current status of clinical trials. Assessing these factors, I discuss how treatable vascular dementia presently is. Use of the term'vascular dementia'is riddled with uncertainties regarding disease classification, and non-standardized diagnostic criteria. There are difficulties in determining the exact relationship between cerebrovascular pathology and cognitive impairment. The comorbid effects of Alzheimer's pathology in some individuals also present an obstacle to reliable clinical diagnosis, and hinder research into effective management approaches. Vascular dementia is preventable and treatable, as there are established primary and secondary prevention measures for the causative cerebrovascular diseases, such as vascular risk factor intervention, antiplatelet therapy, and anticoagulation, amongst others. However, unlike Alzheimer's disease, there are no established symptomatic treatments for vascular dementia. Clinical trials of cholinesterase inhibitors and memantine indicate that they produce small cognitive benefits in patients with vascular dementia, though the exact clinical significance of these is uncertain. Data are insufficient to support the widespread use of these drugs in vascular dementia. Rehabilitation and physical and cognitive exercise may be beneficial, but evidence of cognitive benefit and relief of neuropsychiatric symptoms due to exercise is lacking. PMID:27056862

  6. DOE Waste Treatability Group Guidance

    SciTech Connect

    Kirkpatrick, T.D.

    1995-01-01

    This guidance presents a method and definitions for aggregating U.S. Department of Energy (DOE) waste into streams and treatability groups based on characteristic parameters that influence waste management technology needs. Adaptable to all DOE waste types (i.e., radioactive waste, hazardous waste, mixed waste, sanitary waste), the guidance establishes categories and definitions that reflect variations within the radiological, matrix (e.g., bulk physical/chemical form), and regulated contaminant characteristics of DOE waste. Beginning at the waste container level, the guidance presents a logical approach to implementing the characteristic parameter categories as part of the basis for defining waste streams and as the sole basis for assigning streams to treatability groups. Implementation of this guidance at each DOE site will facilitate the development of technically defined, site-specific waste stream data sets to support waste management planning and reporting activities. Consistent implementation at all of the sites will enable aggregation of the site-specific waste stream data sets into comparable national data sets to support these activities at a DOE complex-wide level.

  7. LABORATORY SCALE STEAM INJECTION TREATABILITY STUDIES

    EPA Science Inventory

    Laboratory scale steam injection treatability studies were first developed at The University of California-Berkeley. A comparable testing facility has been developed at USEPA's Robert S. Kerr Environmental Research Center. Experience has already shown that many volatile organic...

  8. 118-B-1 excavation treatability test plan

    SciTech Connect

    Not Available

    1994-07-01

    The Hanford 118-B-1 Burial Ground Treatability Study has been required by milestone change request {number_sign}M-15-93-04, dated September 30, 1993. The change request requires that a treatability test be conducted at the 100-B Area to obtain additional engineering information for remedial design of burial grounds receiving waste from 100 Area removal actions. This treatability study has two purposes: (1) to support development of the Proposed Plan (PP) and Record of Decision (ROD), which will identify the approach to be used for burial ground remediation, and (2) to provide specific engineering information for receiving waste generated from the 100 Area removal actions. Data generated from this test also will provide critical performance and cost information necessary for remedy evaluation in the detailed analysis of alternatives during preparation of the focused feasibility study (FFS). This treatability testing supports the following 100 Area alternatives: (1) excavation and disposal, and (2) excavation, sorting, (treatment), and disposal.

  9. GUIDE FOR CONDUCTING TREATABILITY STUDIES UNDER CERCLA

    EPA Science Inventory

    Systematically conducted, well-documented treatability studies are an important component of the removal process, remedial investigation/ feasibility study (RI/FS) process and the remedial design/remedial action (RD/RA) process under the Comprehensive Environmental Response...

  10. DEEP VADOSE ZONE TREATABILITY TEST PLAN

    SciTech Connect

    GB CHRONISTER; MJ TRUEX

    2009-07-02

    {sm_bullet} Treatability test plan published in 2008 {sm_bullet} Outlines technology treatability activities for evaluating application of in situ technologies and surface barriers to deep vadose zone contamination (technetium and uranium) {sm_bullet} Key elements - Desiccation testing - Testing of gas-delivered reactants for in situ treatment of uranium - Evaluating surface barrier application to deep vadose zone - Evaluating in situ grouting and soil flushing

  11. 100 area excavation treatability test plan

    SciTech Connect

    Not Available

    1993-05-01

    This test plan documents the requirements for a treatability study on field radionuclide analysis and dust control techniques. These systems will be used during remedial actions involving excavation. The data from this treatability study will be used to support the feasibility study (FS) process. Development and screening of remedial alternatives for the 100 Area, using existing data, have been completed and are documented in the 100 Area Feasibility Study, Phases 1 and 2 (DOE-RL 1992a). Based on the results of the FS, the Treatability Study Program Plan (DOE-RL 1992b) identifies and prioritizes treatability studies for the 100 Area. The data from the treatability study program support future focused FS, interim remedial measures (IRM) selection, operable unit final remedy selection, remedial design, and remedial actions. Excavation is one of the high-priority, near-term, treatability study needs identified in the program plan (DOE-RL 1992b). Excavation of contaminated soils and buried solid wastes is included in several of the alternatives identified in the 100 Area FS. Although a common activity, excavation has only been used occasionally at the Hanford Site for waste removal applications.

  12. Evaporative oxidation treatability test report

    SciTech Connect

    1995-04-01

    In 1992, Congress passed the Federal Facilities Compliance Act that requires the U.S. Department of Energy (DOE) to treat and dispose of its mixed waste in accordance with the Resource Conservation and Recovery Act (RCRA) land disposal restrictions (LDRs). In response to the need for mixed-waste treatment capacity where available off-site commercial treatment facilities do not exist or cannot be used, the DOE Albuquerque Operations Office (DOE-AL) organized a Treatment Selection Team to match mixed wastes with treatment options and develop a strategy for treatment of its mixed wastes. DOE-AL manages operations at nine sites with mixed-waste inventories. The Treatment Selection Team determined a need to develop mobile treatment capacity to treat wastes at the sites where the wastes are generated. Treatment processes used for mixed waste not only must address the hazardous component (i.e., meet LDRs) but also must contain the radioactive component in a form that allows final disposal while protecting workers, the public, and the environment. On the basis of recommendations of the Treatment Selection Team, DOE-AL assigned projects to the sites to bring mixed-waste treatment capacity on-line. The three technologies assigned to the DOE Grand Junction Projects Office (GJPO) are evaporative oxidation, thermal desorption, and treated wastewater evaporation. Rust Geotech, the DOE-GJPO prime contractor, was assigned to design and fabricate mobile treatment units (MTUs) for these three technologies and to deliver the MTUs to selected DOE-AL sites. To conduct treatability tests at the GJPO, Rust leased a pilot-scale evaporative oxidation unit from the Clemson Technical Center (CTC), Anderson, South Carolina. The purpose of this report is to document the findings and results of tests performed using this equipment.

  13. In-Situ Uranium Stabilization Through Polyphosphate Injection: Pilot-Scale Treatability Test at the 300 Area, Hanford Site - 8187

    SciTech Connect

    Vermeul, Vince R.; Fruchter, Jonathan S.; Fritz, Brad G.; Mackley, Rob D.; Wellman, Dawn M.; Williams, Mark D.

    2008-06-02

    This paper describes the pilot-scale treatability test that was conducted to evaluate the efficacy of using a polyphosphate injection approach to treat uranium-contaminated groundwater in situ within the 300 Area aquifer at the Hanford Site in Richland, Washington. Primary test objectives were to assess 1) direct treatment of available uranium contributing to the groundwater plume through precipitation of the uranyl phosphate mineral autunite, and 2) emplacement of secondary-treatment capacity via precipitation of the calcium phosphate mineral apatite, which acts as a long-term sorbent for uranium.

  14. TREATABILITY DATABASE FOR DRINKING WATER CHEMICALS (CCL)

    EPA Science Inventory

    The Treatability Data Base will assemble referenced data on the control of contaminants in drinking water. It will be an interactive data base, housed in an EPA, web-accessible site. It may be used for many purposes, including: identifying an effective treatment process or a se...

  15. THE DRINKING WATER TREATABILITY DATABASE (Slides)

    EPA Science Inventory

    The Drinking Water Treatability Database (TDB) assembles referenced data on the control of contaminants in drinking water, housed on an interactive, publicly-available, USEPA web site (www.epa.gov/tdb). The TDB is of use to drinking water utilities, treatment process design engin...

  16. THE DRINKING WATER TREATABILITY DATABASE (Conference Paper)

    EPA Science Inventory

    The Drinking Water Treatability Database (TDB) assembles referenced data on the control of contaminants in drinking water, housed on an interactive, publicly-available, USEPA web site (www.epa.gov/tdb). The TDB is of use to drinking water utilities, treatment process design engin...

  17. SUPERFUND TREATABILITY CLEARINGHOUSE: COMPOSITING OF EXPLOSIVES

    EPA Science Inventory

    This treatability study was conducted by Atlantic Research Corporation for the U.S. Army Toxic and Hazardous Material Agency. The objective of this bench-scale study was to determine the extent to which TNT and RDX concentrations were reduced by composting for a six week peri...

  18. Factors controlling sulfur concentrations in volcanic apatite

    USGS Publications Warehouse

    Peng, G.; Luhr, J.F.; McGee, J.J.

    1997-01-01

    Apatite crystals from two types of samples were analyzed by electron microprobe for 15 major and trace elements: (1) apatite in H2O- and S-saturated experimental charges of the 1982 El Chicho??n trachyandesite and (2) apatite in volcanic rocks erupted from 20 volcanoes. The SO3 contents of the experimental apatite increase with increasing oxygen fugacity (fo2), from ???0.04 wt% in reduced charges buffered by fayalite-magnetite-quartz (FMQ), to 1.0-2.6 wt% in oxidized charges buffered by manganosite-hausmanite (MNH) or magnetite-hematite (MTH). The SO3 contents of MNH- and MTH-buffered apatite also generally increase with increasing pressure from 2 to 4 kbar and decreasing temperature from 950 to 800??C. The partition coefficient for SO3 between apatite and oxidized melt increases with decreasing temperature but appears to be independent of pressure. Apatites in volcanic rocks show a wide range of SO3 contents (<0.04 to 0.63 wt%). Our sample set includes one group known to contain primary anhydrite and a second group inferred to have been free of primary anhydrite. No systematic differences in apatite S contents are observed between these two groups. Our study was initiated to define the factors controlling S contents in apatite and to evaluate the hypothesis that high S contents in apatite could be characteristic of S-rich anhydrite-bearing magmas such as those erupted from El Chicho??n in 1982 and Pinatubo in 1991. This hypothesis is shown to be invalid, probably chiefly a consequence of the slow intra-crystaline diffusion that limits re-equilibration between early formed apatite and the evolving silicate melt. Contributing factors include early crystallization of most apatite over a relatively small temperature interval, common late-stage magmatic enrichment of S, progressive oxidation during magmatic evolution, and strong controls on S contents in apatite exerted fo2, temperature, and pressure.

  19. 118-B-1 excavation treatability test procedures

    SciTech Connect

    Frain, J.M.

    1994-08-01

    This treatability study has two purposes: to support development of the approach to be used for burial ground remediation, and to provide specific engineering information for the design of burial grounds receiving waste generated from the 100 Area removal actions. Data generated from this test will also provide performance and cost information necessary for detailed analysis of alternatives for burial ground remediation. Further details on the test requirements, milestones and data quality objectives are described in detail in the 118-B-1 Excavation Treatability Test Plan (DOE/RL-94-43). These working procedures are intended for use by field personnel to implement the requirements of the milestone. A copy of the detailed Test Plan will be kept on file at the on-site field support trailer, and will be available for review by field personnel.

  20. Informatics guided Search for Magnetic Apatites

    NASA Astrophysics Data System (ADS)

    Balachandran, Prasanna V.; Lookman, Turab

    2015-03-01

    Materials with apatite crystal structure have applications ranging from biomaterials to electrolytes for solid oxide fuel cells. Their chemical flexibility and structural diversity provide a fertile ground to tune functionalities as potential candidates for many applications. However, magnetic apatites are rare. In this work, we use machine learning methods to rapidly screen a vast chemical space and identify novel apatite compositions with magnetic ions. We first construct a database of known materials from surveying the experimental literature. We then augment the database with features that capture the trends in geometry and bonding characteristics of apatites. Supervised classification learning form the basis of our machine learning approach through which we uncover design rules that enable prediction of potentially stable magnetic apatite compositions, prior to experimental synthesis. Finally, we validate our predictions using density functional theory calculations.

  1. An Injectable Apatite Permeable Reactive Barrier for In Situ 90Sr Immobilization

    SciTech Connect

    Vermeul, Vincent R.; Szecsody, James E.; Fritz, Brad G.; Williams, Mark D.; Moore, Robert C.; Fruchter, Jonathan S.

    2014-04-16

    An injectable permeable reactive barrier (PRB) technology was developed to sequester 90Sr in groundwater through the in situ formation of calcium-phosphate mineral phases, specifically apatite that incorporates 90Sr into the chemical structure. An integrated, multi-scale development and testing approach was used that included laboratory bench-scale experiments, an initial pilot-scale field test, and the emplacement and evaluation of a 300-ft-long treatability-test-scale PRB. Standard groundwater wells were used for emplacement of the treatment zone, allowing treatment of contaminants too deep below ground surface for trench-and-fill type PRB technologies. The apatite amendment formulation uses two separate precursor solutions, one containing a Ca-citrate complex and the other a Na-phosphate solution, to form apatite precipitate in situ. Citrate is needed to keep calcium in solution long enough to achieve a more uniform and areally extensive distribution of precipitate formation. In the summer of 2008, the apatite PRB technology was applied as a 91-m (300-ft) -long permeable reactive barrier on the downgradient edge of a 90Sr plume beneath the Hanford Site in Washington State. The technology was deployed to reduce 90Sr flux discharging to the Columbia River. Performance assessment monitoring data collected to date indicate the barrier is meeting performance objectives. The average reduction in 90Sr concentrations at four downgradient compliance monitoring locations was 95% relative to the high end of the baseline range approximately 1 year after treatment, and continues to meet remedial objectives more than 4 years after treatment.

  2. U-Pb Ages of Lunar Apatites

    NASA Technical Reports Server (NTRS)

    Vaughan, J.; Nemchin, A. A.; Pidgeon, R. T.; Meyer, Charles

    2006-01-01

    Apatite is one of the minerals that is rarely utilized in U-Pb geochronology, compared to some other U-rich accessory phases. Relatively low U concentration, commonly high proportion of common Pb and low closure temperature of U-Pb system of apatite inhibit its application as geochronological tool when other minerals such as zircon are widely available. However, zircon appear to be restricted to certain type of lunar rocks, carrying so called KREEP signature, whereas apatite (and whitlockite) is a common accessory mineral in the lunar samples. Therefore, utilizing apatite for lunar chronology may increase the pool of rocks that are available for U-Pb dating. The low stability of U-Pb systematics of apatite may also result in the resetting of the system during meteoritic bombardment, in which case apatite may provide an additional tool for the study of the impact history of the Moon. In order to investigate these possibilities, we have analysed apatites and zircons from two breccia samples collected during the Apollo 14 mission. Both samples were collected within the Fra Mauro formation, which is interpreted as a material ejected during the impact that formed the Imbrium Basin.

  3. Cyanide analyses for risk and treatability assessments

    SciTech Connect

    MacFarlane, I.D.; Elseroad, H.J.; Pergrin, D.E.; Logan, C.M.

    1994-12-31

    Cyanide, an EPA priority pollutant and target analyte, is typically measured as total. However, cyanide complexation, information which is not acquired through total cyanide analysis, is often a driver of cyanide toxicity and treatability. A case study of a former manufacture gas plant (MGP) is used to demonstrate the usability of various cyanide analytical methods for risk and treatability assessments. Several analytical methods, including cyanide amenable to chlorination and weak acid dissociable cyanide help test the degree of cyanide complexation. Generally, free or uncomplexed cyanide is more biologically available, toxic, and reactive than complexed cyanide. Extensive site testing has shown that free and weakly dissociable cyanide composes only a small fraction of total cyanide as would be expected from the literature, and that risk assessment will be more realistic considering cyanide form. Likewise, aqueous treatment for cyanide can be properly tested if cyanide form is accounted for. Weak acid dissociable cyanide analyses proved to be the most reliable (and potentially acceptable) cyanide method, as well as represent the most toxic and reactive cyanide forms.

  4. Apatite-Melt Partitioning at 1 Bar: An Assessment of Apatite-Melt Exchange Equilibria Resulting from Non-Ideal Mixing of F and Cl in Apatite

    NASA Technical Reports Server (NTRS)

    McCubbin, F. M.; Ustunisik, G.; Vander Kaaden, K. E.

    2016-01-01

    The mineral apatite [Ca5(PO4)3(F,Cl,OH)] is present in a wide range of planetary materials. Due to the presence of volatiles within its crystal structure (X-site), many recent studies have attempted to use apatite to constrain the volatile contents of planetary magmas and mantle sources. In order to use the volatile contents of apatite to precisely determine the abundances of volatiles in coexisting silicate melt or fluids, thermodynamic models for the apatite solid solution and for the apatite components in multi-component silicate melts and fluids are required. Although some thermodynamic models for apatite have been developed, they are incomplete. Furthermore, no mixing model is available for all of the apatite components in silicate melts or fluids, especially for F and Cl components. Several experimental studies have investigated the apatite-melt and apatite-fluid partitioning behavior of F, Cl, and OH in terrestrial and planetary systems, which have determined that apatite-melt partitioning of volatiles are best described as exchange equilibria similar to Fe-Mg partitioning between olivine and silicate melt. However, McCubbin et al. recently reported that the exchange coefficients may vary in portions of apatite compositional space where F, Cl, and OH do not mix ideally in apatite. In particular, solution calorimetry data of apatite compositions along the F-Cl join exhibit substantial excess enthalpies of mixing. In the present study, we conducted apatite-melt partitioning experiments in evacuated, sealed silica-glass tubes at approximately 1 bar and 950-1050 degrees Centigrade on a synthetic Martian basalt composition equivalent to the basaltic shergottite Queen Alexandria Range (QUE) 94201. These experiments were conducted dry, at low pressure, to assess the effects of temperature and apatite composition on the partitioning behavior of F and Cl between apatite and basaltic melt along the F-Cl apatite binary join, where there is non-ideal mixing of F and Cl

  5. Water-mediated structuring of bone apatite.

    PubMed

    Wang, Yan; Von Euw, Stanislas; Fernandes, Francisco M; Cassaignon, Sophie; Selmane, Mohamed; Laurent, Guillaume; Pehau-Arnaudet, Gérard; Coelho, Cristina; Bonhomme-Coury, Laure; Giraud-Guille, Marie-Madeleine; Babonneau, Florence; Azaïs, Thierry; Nassif, Nadine

    2013-12-01

    It is well known that organic molecules from the vertebrate extracellular matrix of calcifying tissues are essential in structuring the apatite mineral. Here, we show that water also plays a structuring role. By using solid-state nuclear magnetic resonance, wide-angle X-ray scattering and cryogenic transmission electron microscopy to characterize the structure and organization of crystalline and biomimetic apatite nanoparticles as well as intact bone samples, we demonstrate that water orients apatite crystals through an amorphous calcium phosphate-like layer that coats the crystalline core of bone apatite. This disordered layer is reminiscent of those found around the crystalline core of calcified biominerals in various natural composite materials in vivo. This work provides an extended local model of bone biomineralization. PMID:24193662

  6. A Systematic Description of Apatite Frameworks

    NASA Astrophysics Data System (ADS)

    White, T.

    2006-05-01

    Apatites of various chemistries are potentially important in chemical synthesis, clean energy and environmental remediation. The so-called 'lacunary' apatites are prospective fuel cell electrolytes, while silver analogues are potential photocatalysts, and radiation resistant silicate apatites can retain nuclear wastes. Although apatites have one-dimensional channels, as distinct from the three-dimensional channels in classic zeolites, they do display several zeolitic features including: a framework which can be tuned to accommodate different tunnel contents; an ability to accept large cations of different valance through the introduction of framework counter ions; and reversible ion exchange for some anions and cations. Most recently, it has been recognized, in both natural and synthetic materials, that intergrowth of tunnels of different size at the nanoscale is possible, a feature with important technology performance implications. This paper describes a new approach for the structural derivation of apatites from an idealized prototype that correlates chemistry and tunnel geometry, and in so doing, permits the design of new apatites and prediction of their properties.

  7. In Situ Vitrification Treatability Study Work Plan

    SciTech Connect

    Charboneau, B.L.; Landon, J.L.

    1989-03-01

    The Buried Waste Program was established in October, 1987 to accelerate the studies needed to develop a recommended long-term management plan for the buried mixed waste at the Radioactive Waste Management Complex at the Idaho National Engineering Laboratory. The In Situ Vitrification Project is being conducted in a Comprehensive Environmental Response, Compensation, and Liability Act Feasibility Study format to identify methods for the long-term management of the mixed waste buried. This In Situ Vitrification Treatability Study Work Plan gives a brief description of the site, work breakdown structure, and project organization: the in situ vitrification technology; the purpose of the tests and demonstrations; and the equipment and materials required for the tests and demonstration. 5 refs., 6 figs., 3 tabs.

  8. Apatite Formation: Why It May Not Work as Planned, and How to Conclusively Identify Apatite Compounds

    PubMed Central

    2013-01-01

    Calcium phosphate apatites are inorganic compounds encountered in many different mineralized tissues. Bone mineral, for example, is constituted of nanocrystalline nonstoichiometric apatite, and the production of “analogs” through a variety of methods is frequently reported. In another context, the ability of solid surfaces to favor the nucleation and growth of “bone-like” apatite upon immersion in supersaturated fluids such as SFB is commonly used as one evaluation index of the “bioactivity” of such surfaces. Yet, the compounds or deposits obtained are not always thoroughly characterized, and their apatitic nature is sometimes not firmly assessed by appropriate physicochemical analyses. Of particular importance are the “actual” conditions in which the precipitation takes place. The precipitation of a white solid does not automatically indicate the formation of a “bone-like carbonate apatite layer” as is sometimes too hastily concluded: “all that glitters is not gold.” The identification of an apatite phase should be carefully demonstrated by appropriate characterization, preferably using complementary techniques. This review considers the fundamentals of calcium phosphate apatite characterization discussing several techniques: electron microscopy/EDX, XRD, FTIR/Raman spectroscopies, chemical analyses, and solid state NMR. It also underlines frequent problems that should be kept in mind when making “bone-like apatites.” PMID:23984373

  9. SOIL WASHING TREATABILITY TESTS FOR PESTICIDE- CONTAMINATED SOIL

    EPA Science Inventory

    The 1987 Sand Creek Operable Unit 5 record of decision (ROD) identified soil washing as the selected technology to remediate soils contaminated with high levels of organochlorine pesticides, herbicides, and metals. Initial treatability tests conducted to assess the applicability...

  10. TREATABILITY STUDIES OF PESTICIDE MANUFACTURING WASTEWATERS: ETHYLENEBISDITHIOCARBAMATE FUNGICIDES

    EPA Science Inventory

    The report gives results of laboratory and pilot studies on the biological treatability of wastewaters from the manufacture of ethylenebisdithiocarbamate (EBDC) fungicide. At concentration levels representative of EBDC production units and total plant wastewaters discharged to pu...

  11. EPA's Drinking Water Treatability Database and Treatment Cost Models

    EPA Science Inventory

    USEPA Drinking Water Treatability Database and Drinking Water Treatment Cost Models are valuable tools for determining the effectiveness and cost of treatment for contaminants of emerging concern. The models will be introduced, explained, and demonstrated.

  12. Treatability Test Plan for an In Situ Biostimulation Reducing Barrier

    SciTech Connect

    Truex, Michael J.; Vermeul, Vince R.; Long, Philip E.; Brockman, Fred J.; Oostrom, Mart; Hubbard, Susan; Borden, Robert C.; Fruchter, Jonathan S.

    2007-07-21

    This treatability test plan supports a new, integrated strategy to accelerate cleanup of chromium in the Hanford 100 Areas. This plan includes performing a field-scale treatability test for bioreduction of chromate, nitrate, and dissolved oxygen. In addition to remediating a portion of the plume and demonstrating reduction of electron acceptors in the plume, the data from this test will be valuable for designing a full-scale bioremediation system to apply at this and other chromium plumes at Hanford.

  13. The volatile content of Vesta: Clues from apatite in eucrites

    NASA Astrophysics Data System (ADS)

    Sarafian, Adam Robert; Roden, Michael F.; PatiñO-Douce, Alberto E.

    2013-11-01

    Apatite was analyzed by electron microprobe in 3 cumulate and 10 basaltic eucrites. Eucritic apatite is fluorine-rich with minor chlorine and hydroxyl (calculated by difference). We confirmed the hydroxyl content by measuring hydroxyl directly in apatites from three representative eucrites using secondary ionization mass spectroscopy. Overall, most eucritic apatites resemble fluorine-rich lunar mare apatites, but intriguing OH- and Cl-rich apatites suggest a role for water and/or hydrothermal fluids in the Vestan interior or on other related differentiated asteroids. Most late-stage apatite found in mesostasis has little hydroxyl or chlorine and is thought to have crystallized from a degassed magma; however, several apatites exhibit atypical compositions and/or textural characteristics. For example, the isotopically anomalous basaltic eucrite Pasamonte has apatite in the mesostasis with significant OH. Apatites in Juvinas also have significant OH and occur as veinlets crosscutting silicates. Euhedral apatites in the Moore County cumulate eucrite occur as inclusions in pyroxene and are also hydroxyl-rich (0.62 wt% OH). The OH was confirmed by SIMS analysis and this apatite clearly points to the presence of water, at least locally, in the Vestan interior. Portions of Elephant Moraine (EET) 90020 have large and abundant apatites, which may be the product of apatite accumulation in a zone of melt-rock reaction. Relatively chlorine-rich apatites occur in basaltic eucrite Graves Nunataks (GRA) 98098 (approximately 1 wt% Cl). Particularly striking is the compositional similarity between apatite in GRA 98098 and apatites in lunar KREEP, which may indicate the presence of residual magmas from an asteroid-wide magma ocean on Vesta.

  14. Ultrastructural analyses of nanoscale apatite biomimetically grown on organic template

    PubMed Central

    Hong, S.I.; Lee, K.H.; Outslay, M.E.; Kohn, D.H.

    2009-01-01

    The ultrastructure of nanoscale apatite biomimetically formed on an organic template from a supersaturated mineralizing solution was studied to examine the morphological and crystalline arrangement of mineral apatites. Needle-shaped apatite crystal plates with a size distribution of ~100 to ~1000 nm and the long axis parallel to the c axis ([002]) were randomly distributed in the mineral films. Between these randomly distributed needle-shaped apatite crystals, amorphous phases and apatite crystals (~20–40 nm) with the normal of the grains quasi-perpendicular to the c axis were observed. These observations suggest that the apatite film is an interwoven structure of amorphous phases and apatite crystals with various orientations. The mechanisms underlying the shape of the crystalline apatite plate and aggregated apatite nodules are discussed from an energy-barrier point of view. The plate or needle-shaped apatite is favored in single-crystalline form, whereas the granular nodules are favored in the polycrystalline apatite aggregate. The similarity in shape in both single-crystalline needle-shaped apatite and polycrystalline granular apatite over a wide range of sizes is explained by the principle of similitude, in which the growth and shape are determined by the forces acting upon the surface area and the volume. PMID:19763228

  15. Calibration for Infrared Measurements of Water in Apatite

    NASA Astrophysics Data System (ADS)

    Wang, K. L.; Xu, Z.; Zhang, Y.

    2010-03-01

    We report a study on calibration of infrared (IR) method to determine water concentration in apatite using the elastic recoil detection (ERD) method. The calibration will allow us to constrain water content in lunar and martian apatites using IR spectra.

  16. In-Situ Uranium Stabilization Through Polyphosphate Injection: Pilot-Scale Treatability Test at the 300 Area, Hanford Site

    SciTech Connect

    Vermeul, V.R.; Fruchter, J.S.; Fritz, B.G.; Mackley, R.D.; Wellman, D.M.; Williams, M.D.

    2008-07-01

    This paper describes the pilot-scale treatability test that was conducted to evaluate the efficacy of using a polyphosphate injection approach to treat uranium-contaminated groundwater in situ within the 300 Area aquifer at the Hanford Site in Richland, Washington. Primary test objectives were to assess 1) direct treatment of available uranium contributing to the groundwater plume through precipitation of the uranyl-phosphate mineral autunite, and 2) emplacement of secondary-treatment capacity via precipitation of the calcium-phosphate mineral apatite, which acts as a long-term sorbent for uranium. Based on an injection design analysis that incorporated results from both bench-scale testing and site-specific characterization activities, a three-phase injection approach was selected for field-scale testing. This approach consisted of 1) an initial polyphosphate injection to facilitate direct treatment of aqueous uranium in the pore space, 2) a second phase consisting of a calcium chloride injection to provide an available calcium source for the creation of apatite, and 3) a subsequent polyphosphate injection to supply a phosphate source for the formation of apatite. The total-solution volume injected during this field test was approximately 3.8 million L (1 million gal). Results from this investigation will be used to identify implementation challenges and investigate the technology's ability to meet remedial objectives. In addition, data from this test will provide valuable information for designing a full-scale remedial action for uranium in groundwater beneath the 300 Area of the Hanford Site, and a detailed understanding of the fundamental underpinnings necessary to evaluate the efficacy and potential for utilization of the polyphosphate technology at other sites with varying geochemical and hydrodynamic conditions. (authors)

  17. IN SITU LEAD IMMOBILIZATION BY APATITE

    EPA Science Inventory

    Lead contamination is of environmental concern due to its effect on human health. he purpose of this study was to develop a technology to immobilize Pb in situ in contaminated soils and wastes using apatite. ydroxyapatite [Ca10(PO4)6(OH)2]was reacted with aqueous Pb, resinexchang...

  18. IN SITU LEAD IMMOBILIZATION BY APATITE

    EPA Science Inventory

    Lead contamination is of environmental concern due to its effect on human health. The purpose of this study was to develop a technology to immobilize Pb in situ in contaminated soils and wastes using apatite. Hydroxyapatite [Ca10(PO4)6(O...

  19. 100 Area groundwater biodenitrification bench-scale treatability study procedures

    SciTech Connect

    Peyton, B.M.; Martin, K.R.

    1993-05-01

    This document describes the methodologies and procedures for conducting the bench-scale biodenitrification treatability tests at Pacific Northwest Laboratory{sup a} (PNL). Biodenitrification is the biological conversion of nitrate and nitrite to gaseous nitrogen. The tests will use statistically designed batch studies to determine if biodenitrification can reduce residual nitrate concentrations to 45 mg/L, the current maximum contaminant level (MCL). These tests will be carried out in anaerobic flasks with a carbon source added to demonstrate nitrate removal. At the pilot scale, an incremental amount of additional carbon will be required to remove the small amount of oxygen present in the incoming groundwater. These tests will be conducted under the guidance of Westinghouse Hanford Company (WHC) and the 100-HR-3 Groundwater Treatability Test Plan (DOE/RL-92-73) and the Treatability Study Program Plan (DOE/RL-92-48) using groundwater from 100-HR-3. In addition to the procedures, requirements for safety, quality assurance, reporting, and schedule are given. Appendices include analytical procedures, a Quality Assurance Project Plan, a Health and Safety Plan, and Applicable Material Data Safety Sheets. The procedures contained herein are designed specifically for the 100-HR-3 Groundwater Treatability Test Plan, and while the author believes that the methods described herein are scientifically valid, the procedures should not be construed or mistaken to be generally applicable to any other treatability study.

  20. Can Polyphosphate Biochemistry Affect Biological Apatite Saturation?

    NASA Astrophysics Data System (ADS)

    Omelon, S. J.; Matsuura, N.; Gorelikov, I.; Wynnyckyj, C.; Grynpas, M. D.

    2010-12-01

    Phosphorus (P) is an important and limiting element for life. One strategy for storing ortho phosphates (Pi) is polymerization. Polymerized Pi's (polyphosphates: (PO3-)n: polyPs) serve as a Pi bank, as well as a catiion chelator, energy source, & regulator of responses to stresses in the stationary phase of culture growth and development1. PolyP biochemistry has been investigated in yeasts, bacteria & plants2. Bigeochemical cycling of P includes the condensation of Pi into pyro (P2O7-4), & polyPs, & the release of Pi from these compounds by the hydrolytic degradation of Pi from phosphomonoester bonds. Alkaline phosphatase (ALP) is one of the predominate enzymes for regenerating Pi in aquatic systems3, & it cleaves Pi from polyPs. ALP is also the enzyme associated with apatite biomineralization in vertebrates4. PolyP was proposed to be the ALP substrate in bone mineralization5. Where calcium ions are plentiful in many aquatic environments, there is no requirement for aquatic life to generate Ca-stores. However, terrestrial vertebrates benefit from a bioavailable Ca-store such as apatite. The Pi storage strategy of polymerizing PO4-3 into polyPs dovetails well with Ca-banking, as polyPs sequester Ca, forming a neutral calcium polyphosphate (Ca-polyP: (Ca(PO3)2)n) complex. This neutral complex represents a high total [Ca+2] & [PO4-3], without the threat of inadvertent apatite precipitation, as the free [Ca+2] & [PO4-3], and therefore apatite saturation, are zero. Recent identification of polyP in regions of bone resorption & calcifying cartilage5 suggests that vertebrates may use polyP chemistry to bank Ca+2 and PO4-3. In vitro experiments with nanoparticulate Ca-polyP & ALP were undertaken to determine if carbonated apatite could precipitate from 1M Ca-polyP in Pi-free “physiological fluid” (0.1 M NaCl, 2 mM Ca+2, 0.8 mM Mg+2, pH ~8.0 ±0.5, 37 °C), as this is estimated to generate the [Ca+2] & [PO4-3] required to form the apatite content of bone tissue

  1. Waste treatability guidance program. User`s guide. Revision 0

    SciTech Connect

    Toth, C.

    1995-12-21

    DOE sites across the country generate and manage radioactive, hazardous, mixed, and sanitary wastes. It is necessary for each site to find the technologies and associated capacities required to manage its waste. One role of DOE HQ Office of Environmental Restoration and Waste Management is to facilitate the integration of the site- specific plans into coherent national plans. DOE has developed a standard methodology for defining and categorizing waste streams into treatability groups based on characteristic parameters that influence waste management technology needs. This Waste Treatability Guidance Program automates the Guidance Document for the categorization of waste information into treatability groups; this application provides a consistent implementation of the methodology across the National TRU Program. This User`s Guide provides instructions on how to use the program, including installations instructions and program operation. This document satisfies the requirements of the Software Quality Assurance Plan.

  2. GUIDE FOR CONDUCTING TREATABILITY STUDIES UNDER CERCLA: SOLVENT EXTRACTION QUICK REFERENCE FACT SHEET

    EPA Science Inventory

    Systematically conducted, well-documented treatability studies are an important component of remedy evaluation and selection under the Superfund Program. his fact sheet focuses on solvent extraction treatability studies, and is highly abridged version of the guide which bears the...

  3. GUIDE FOR CONDUCTING TREATABILITY STUDIES UNDER CERCLA: CHEMICAL DEHALOGENATION (QUICK REFERENCE FACT SHEET)

    EPA Science Inventory

    Systematically conducted, well-documented treatability studies are an important component of remedy evaluation and selection under the Superfund program. his manual focuses on chemical dehalogenation treatability studies conducted in support of remedy selection that is conducted ...

  4. Sulfur evolution of the 1991 Pinatubo magmas based on apatite

    NASA Astrophysics Data System (ADS)

    Van Hoose, Ashley E.; Streck, Martin J.; Pallister, John S.; Wälle, Markus

    2013-05-01

    Using electron microprobe (EMP) and laser-ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) to collect major and rare-earth elements (REE), respectively, from apatites from the 1991 Mt. Pinatubo juvenile eruption products, we have determined that two statistically distinct populations of apatite exist. One population crystallized from the juvenile basaltic melt (basalt apatites) and the other population crystallized from the main dacitic magma body (silicic apatites). Both populations contain high-S apatites (> 0.7 wt.% SO3). Apatite has previously been shown to be a potential monitor for magmatic sulfur contents via numerous proposed coupled substitutions of P5 + for S6 +. However, simple apatite/melt partitioning cannot account for high-S silicic apatites, which grew from a silicic melt with an apparent maximum S concentration of ~ 80 ppm. Disparate apatite morphology (i.e. skeletal and acicular for basalt apatites and euhedral for silicic apatites) as well as compositional evidence reveal that high-S silicic apatites were not inherited from the juvenile basalt during mingling/mixing prior to eruption. Sulfur gain from neighboring anhydrite phenocrysts can also be ruled-out as a source of high sulfur. EMP sulfur mapping of silicic apatites shows highly irregular patterns of sulfur enrichment that do not correspond with adjacent anhydrite and can be found within apatites hosted by other minerals (e.g. hornblende and Fe-Ti oxides). With these data in mind, we propose high-S silicic apatites from Pinatubo and other sulfur-rich systems achieved elevated sulfur concentrations during high sulfur fluxing events that originated from underplated basalt during degassing of a SO2-rich fluid phase. That basalts were indeed sulfur rich and oxidized is here indicated by high S contents of apatites growing in basalt. The predominant location of S-rich areas of silicic apatite is crystal interiors of apatite inclusions in other mineral phases, while large apatite

  5. Knowing hypertension and diabetes: Conditions of treatability in Uganda.

    PubMed

    Whyte, Susan Reynolds

    2016-05-01

    In Uganda, hypertension and diabetes have only recently been included in the health policy agenda. As they become treatable disorders, they take on more distinct contours in people's minds. This article relates knowledge about these two conditions to health institutions and technology for diagnosing and treating them. The response to the AIDS epidemic in Uganda provides an important context for, and contrast with, the emergence of hypertension and diabetes as social phenomena. Ethnographic fieldwork shows the interplay between experience of these conditions and the political economy of treatability. PMID:26233676

  6. Treatability Test Plan for an In Situ Biostimulation Reducing Barrier

    SciTech Connect

    Truex, Michael J.; Vermeul, Vince R.; Long, Philip E.; Brockman, Fred J.; Oostrom, Mart; Hubbard, Susan; Borden, Robert C.; Fruchter, Jonathan S.

    2007-10-26

    This treatability test plan supports a new, integrated strategy to accelerate cleanup of chromium in the 100 Areas at the Hanford Site. This plan includes performing a field-scale treatability test for bioreduction of chromate, nitrate, and dissolved oxygen. In addition to remediating a portion of the plume and demonstrating reduction of electron acceptors in the plume, the data from this test will be valuable for designing a full-scale bioremediation system to apply at this and other chromium plumes at the Hanford Site.

  7. Lunar apatite with terrestrial volatile abundances.

    PubMed

    Boyce, Jeremy W; Liu, Yang; Rossman, George R; Guan, Yunbin; Eiler, John M; Stolper, Edward M; Taylor, Lawrence A

    2010-07-22

    The Moon is thought to be depleted relative to the Earth in volatile elements such as H, Cl and the alkalis. Nevertheless, evidence for lunar explosive volcanism has been used to infer that some lunar magmas exsolved a CO-rich and CO(2)-rich vapour phase before or during eruption. Although there is also evidence for other volatile species on glass spherules, until recently there had been no unambiguous reports of indigenous H in lunar rocks. Here we report quantitative ion microprobe measurements of late-stage apatite from lunar basalt 14053 that document concentrations of H, Cl and S that are indistinguishable from apatites in common terrestrial igneous rocks. These volatile contents could reflect post-magmatic metamorphic volatile addition or growth from a late-stage, interstitial, sulphide-saturated melt that contained approximately 1,600 parts per million H(2)O and approximately 3,500 parts per million Cl. Both metamorphic and igneous models of apatite formation suggest a volatile inventory for at least some lunar materials that is similar to comparable terrestrial materials. One possible implication is that portions of the lunar mantle or crust are more volatile-rich than previously thought. PMID:20651686

  8. TREATABILITY POTENTIAL FOR EPA LISTED HAZARDOUS WASTES IN SOIL

    EPA Science Inventory

    This study developed comprehensive screening data on the treatability in soil of: (a) specific listed hazardous organic chemicals, and (b) waste sludge from explosives production (K044) and related chemicals. Laboratory experiments were conducted using two soil types, an acidic s...

  9. LOSS OF ORGANIC CHEMICALS IN SOIL: PURE COMPOUND TREATABILITY STUDIES

    EPA Science Inventory

    Comprehensive screening data on the treatability of 32 organic chemicals in soil were developed. Of the evaluated chemicals, 22 were phenolic compounds. Aerobic batch laboratory microcosm experiments were conducted using two soils: an acidic clay soil with <1% organic matter and ...

  10. The expanded amelogenin polyproline region preferentially binds to apatite versus carbonate and promotes apatite crystal elongation

    PubMed Central

    Gopinathan, Gokul; Jin, Tianquan; Liu, Min; Li, Steve; Atsawasuwan, Phimon; Galang, Maria-Therese; Allen, Michael; Luan, Xianghong; Diekwisch, Thomas G. H.

    2014-01-01

    The transition from invertebrate calcium carbonate-based calcite and aragonite exo- and endoskeletons to the calcium phosphate-based vertebrate backbones and jaws composed of microscopic hydroxyapatite crystals is one of the great revolutions in the evolution of terrestrial organisms. To identify potential factors that might have played a role in such a transition, three key domains of the vertebrate tooth enamel protein amelogenin were probed for calcium mineral/protein interactions and their ability to promote calcium phosphate and calcium carbonate crystal growth. Under calcium phosphate crystal growth conditions, only the carboxy-terminus augmented polyproline repeat peptide, but not the N-terminal peptide nor the polyproline repeat peptide alone, promoted the formation of thin and parallel crystallites resembling those of bone and initial enamel. In contrast, under calcium carbonate crystal growth conditions, all three amelogenin-derived polypeptides caused calcium carbonate to form fused crystalline conglomerates. When examined for long-term crystal growth, polyproline repeat peptides of increasing length promoted the growth of shorter calcium carbonate crystals with broader basis, contrary to the positive correlation between polyproline repeat element length and apatite mineralization published earlier. To determine whether the positive correlation between polyproline repeat element length and apatite crystal growth versus the inverse correlation between polyproline repeat length and calcium carbonate crystal growth were related to the binding affinity of the polyproline domain to either apatite or carbonate, a parallel series of calcium carbonate and calcium phosphate/apatite protein binding studies was conducted. These studies demonstrated a remarkable binding affinity between the augmented amelogenin polyproline repeat region and calcium phosphates, and almost no binding to calcium carbonates. In contrast, the amelogenin N-terminus bound to both carbonate

  11. Chitosan/apatite composite beads prepared by in situ generation of apatite or Si-apatite nanocrystals.

    PubMed

    Davidenko, Natalia; Carrodeguas, Raúl G; Peniche, Carlos; Solís, Yaimara; Cameron, Ruth E

    2010-02-01

    The objective of this work was to develop nanocrystalline apatite (Ap) dispersed in a chitosan (CHI) matrix as a material for applications in bone tissue engineering. CHI/Ap composites of different weight ratios (20/80, 50/50 and 80/20) and with CHI of different molecular weights were prepared by a biomimetic stepwise route. Firstly, CaHPO(4).2H(2)O (DCPD) crystals were precipitated from Ca(CH(3)COO)(2) and NaHPO(4) in the bulk CHI solution, followed by the formation of CHI/DCPD beads by coacervation. The beads were treated with Na(3)PO(4)/Na(5)P(3)O(10) solution (pH 12-13) to crosslink the CHI and to hydrolyse the DCPD to nanocrystalline Ap. This new experimental procedure ensured that complete conversion of DCPD into sodium-substituted apatite was achieved without appreciable increases in its crystallinity and particle size. In addition, composites with silicon-doped Ap were prepared by substituting Na(3)PO(4) by Na(2)SiO(3) in the crosslinking/hydrolysis step. Characterization of the resultant composites by scanning electron microscopy, X-ray powder diffraction (XRD), thermal analysis and Fourier transform infrared spectroscopy confirmed the formation, within the CHI matrix, of nanoparticles of sodium- and carbonate-substituted hydroxyapatite [Ca(10-x)Na(x)(PO(4))(6-x)(CO(3))(x)(OH)(2)] with diameters less than 20nm. Relatively good correspondence was shown between the experimentally determined inorganic content and that expected theoretically. Structural data obtained from its XRD patterns revealed a decrease in both crystal domain size and cell parameters of Ap formed in situ with increasing CHI content. It was found that the molecular weight of CHI and silicate doping both affected the nucleation and growth of apatite nanocrystallites. These effects are discussed in detail. PMID:19632363

  12. Distribution of halogens during fluid-mediated apatite replacement

    NASA Astrophysics Data System (ADS)

    Kusebauch, Christof; John, Timm; Whitehouse, Martin J.

    2016-04-01

    Apatite (Ca5(PO4)3(F,Cl,OH)) is one the most abundant halogen containing minerals in the crust. It is present in many different rock types and stable up to P-T conditions of the mantle. Although probably not relevant for the halogen budget of the mantle, apatite is potentially a carrier phase of halogens into the mantle via subduction processes and therefore important for the global halogen cycle. Different partitioning behavior of the halogens between apatite and melt/fluids causes fractionation of these elements. In hydrothermal environments apatite reacts via a coupled dissolution-reprecipitation process that leads to apatite halogen compositions which are in (local) equilibrium with the hydrothermal fluid. This behavior enables apatite to be used as fluid probe and as a tool for tracking fluid evolution during fluid-rock interaction. Here, we present a combined experimental and field related study focused on replacement of apatite under hydrothermal conditions, to investigate the partitioning of halogens between apatite and fluids. Experiments were conducted in a cold seal pressure apparatus at 0.2 GPa and temperatures ranging from 400-700°C using halogen bearing solutions of different composition (KOH, NaF, NaCl, NaBr, NaI) to promote the replacement of Cl-apatite. The halogen composition of reacted apatite was analyzed by electron microprobe (EMPA) and secondary ion mass spectrometry (SIMS). The data was used to calculate partition coefficients of halogens between fluid and apatite. Our new partitioning data show that fluorine is the most compatible halogen followed by chlorine, bromine and iodine. Comparison between partition coefficients of the apatite-fluid system and coefficients derived in the apatite-melt system reveals values for F that are one to two orders of magnitude higher. In contrast, Cl and Br show a similar partition behavior in fluid and melt systems. Consequently, apatite that formed by fluid-rock interaction will fractionate F from Cl more

  13. Hanford Site Annual Treatability Studies Report, Calendar Year 2002

    SciTech Connect

    Grohs, Eugene L.

    2003-02-28

    This report provides information required to be reported annually by the Washington Administrative Code (WAC) 173-303-071 (3)(r)(ii)(F) and (3)(s)(ix) on the treatability studies conducted on the Hanford Site in 2002. These studies were conducted as required by WAC 173-303-071, “Excluded Categories of Waste,” sections (3)(r) and (s). Unless otherwise noted, the waste samples were provided by and the treatability studies were performed for the U.S. Department of Energy, Richland Operations Office, P.O. Box 550, Richland, Washington 99352. The U.S. Environmental Protection Agency identification number for these studies is WA7890008967.

  14. Treatability of manganese by sodium silicate and chlorine

    SciTech Connect

    Robinson, F.B.; Ronk, S.K. )

    1987-11-01

    Manganese sequestering by nearly simultaneous additions of sodium silicate and sodium hypochlorite was studied in laboratory-prepared waters. Under conditions of near-neutral pH and 150-250 mg/liter of alkalinity as CaCO{sub 3}, 1-2 mg manganese/liter could be sequestered for up to one day. Less effective manganese treatability was found at pH 8 than at pH 7. Additionally, at pH 7 the best results were obtained when neither silicate nor hypochlorite was added because of the slow manganese oxidation rate by oxygen alone. Aging of diluted stock silicate solutions prior to dosing also resulted in poor treatment; the presence of background silica increased the treatment effectiveness only slightly. Overall, manganese was less treatable by this method than iron under the same treatment conditions.

  15. Rare earth elements materials production from apatite ores

    NASA Astrophysics Data System (ADS)

    Anufrieva, A. V.; Andrienko, O. S.; Buynovskiy, A. S.; Makaseev, Y. N.; Mazov, I. N.; Nefedov, R. A.; Sachkov, V. I.; Stepanova, O. B.; Valkov, A. V.

    2016-01-01

    The paper deals with the study of processing apatite ores with nitric acid and extraction of the rare earth elements. The rare earth elements can be successfully separated and recovered by extraction from the nitrate- phosphate solution, being an tributyl phosphate as extraction agent. The developed scheme of the processing apatite concentrate provides obtaining rare earth concentrates with high qualitative characteristics.

  16. Psychiatric manifestations of treatable hereditary metabolic disorders in adults

    PubMed Central

    2014-01-01

    Detecting psychiatric disorders of secondary origin is a crucial concern for the psychiatrist. But how can this reliably be done among a large number of conditions, most of which have a very low prevalence? Metabolic screening undertaken in a population of subjects with psychosis demonstrated the presence of treatable metabolic disorders in a significant number of cases. The nature of the symptoms that should alert the clinician is also a fundamental issue and is not limited to psychosis. Hereditary metabolic disorders (HMD) are a rare but important cause of psychiatric disorders in adolescents and adults, the signs of which may remain isolated for years before other more specific organic signs appear. HMDs that present purely with psychiatric symptoms are very difficult to diagnose due to low awareness of these rare diseases among psychiatrists. However, it is important to identify HMDs in order to refer patients to specialist centres for appropriate management, disease-specific treatment and possible prevention of irreversible physical and neurological complications. Genetic counselling can also be provided. This review focuses on three HMD categories: acute, treatable HMDs (urea cycle abnormalities, remethylation disorders, acute intermittent porphyria); chronic, treatable HMDs (Wilson’s disease, Niemann-Pick disease type C, homocystinuria due to cystathionine beta-synthase deficiency, cerebrotendinous xanthomatosis); and chronic HMDs that are difficult to treat (lysosomal storage diseases, X-linked adrenoleukodystrophy, creatine deficiency syndrome). We also propose an algorithm for the diagnosis of HMDs in patients with psychiatric symptoms. PMID:25478001

  17. Strongly bound citrate stabilizes the apatite nanocrystals in bone

    SciTech Connect

    Hu, Y.-Y.; Rawal, A.; Schmidt-Rohr, K.

    2010-10-12

    Nanocrystals of apatitic calcium phosphate impart the organic-inorganic nanocomposite in bone with favorable mechanical properties. So far, the factors preventing crystal growth beyond the favorable thickness of ca. 3 nm have not been identified. Here we show that the apatite surfaces are studded with strongly bound citrate molecules, whose signals have been identified unambiguously by multinuclear magnetic resonance (NMR) analysis. NMR reveals that bound citrate accounts for 5.5 wt% of the organic matter in bone and covers apatite at a density of about 1 molecule per (2 nm){sup 2}, with its three carboxylate groups at distances of 0.3 to 0.45 nm from the apatite surface. Bound citrate is highly conserved, being found in fish, avian, and mammalian bone, which indicates its critical role in interfering with crystal thickening and stabilizing the apatite nanocrystals in bone

  18. Apatite as a Tool for Tracking Magmatic CO2 Contents

    NASA Astrophysics Data System (ADS)

    Riker, J.; Humphreys, M.; Brooker, R. A.

    2014-12-01

    CO2 plays a fundamental role in the evolution of magmatic and volcanic systems, but its low solubility in silicate melts means that direct records of magmatic CO2 concentrations remain elusive. The phosphate mineral apatite is unique among igneous minerals in its capacity to accommodate all major magmatic volatiles (H2O, F, Cl, CO2 and S). Although interest in apatite as a tool for tracking magmatic volatile contents (namely H2O, F, and Cl) has increased in recent years, its potential as a record of magmatic CO2contents remains untapped. We present the results of high-temperature, high-pressure experiments investigating the partitioning behaviour of CO2 between apatite and basaltic melt. Experiments were run in piston cylinder apparatus at 1 GPa and 1250 °C, with a slow initial cooling ramp employed to facilitate crystal growth. Each charge contained the starting basaltic powder doped with Ca-phosphate and variable proportions of H2O, CO2, and F. Run products are glass-rich charges containing 15-25 vol% large, euhedral apatite crystals (± cpx and minor biotite). Experimental apatites and glasses have been characterised by BSE imaging, electron microprobe, and ion microprobe. Apatites range in composition from near-endmember fluorapatite (3.0 wt% F), to near-endmember hydroxyapatite (1.7 wt% H2O), to carbon-rich apatite containing up to 1.6 wt% CO2. Apatite compositions are stoichiometric if all anions (F-, OH-, and CO32—) lie in the channel site, suggesting an "A-type" substitution under these conditions (i.e. CO32— + [] = 2X—, where X is another channel anion and [] is a vacancy; e.g. Fleet et al. 2004). Importantly, CO2 partitions readily into apatite at all fluid compositions considered here. CO2 is also more compatible in apatite than water at our run conditions, with calculated H2O-CO2 exchange coefficients close to or greater than 1. Our results indicate that when channel ions are primarily occupied by H2O and CO2 (i.e. F- and Cl-poor magmatic systems

  19. Production of spherical apatite powders—the first step for optimized thermal-sprayed apatite coatings

    NASA Astrophysics Data System (ADS)

    Lugscheider, E.; Knepper, M.; Gross, K. A.

    1992-09-01

    Regardless of the thermal spraying system, a coating can only be as good as the quality of the input powders. Powder quality in turn is dependent on the manufacturing process and conditions. Thus, it is possible to alter characteristics such as morphology, porosity, phase composition, and the mechanical strength of the individual particles. This article looks at powder agglomerations using the spray drying technique. Two different spray drying configurations were used to produce spherical apatite powders. Apatite powders could be produced with variable densities. Rotary-atomized powders possessed internal porosity as well as open porosity. More applicable for thermal spraying are the nozzle-atomized powders, which are more dense. The particle size range produced is dependent on the many parameters in the spray drying process. Hydroxyapatite is more sensitive than fluorapatite to alterations in process conditions. The powders produced were clean, free of other phases, and possessed good flowability for thermal spraying purposes.

  20. Guide for conducting treatability studies under CERCLA: Solvent extraction quick reference fact sheet

    SciTech Connect

    Rawe, J.

    1992-08-01

    Systematically conducted, well-documented treatability studies are an important component of remedy evaluation and selection under the Superfund Program. This fact sheet focuses on solvent extraction treatability studies, and is a highly abridged version of the guide which bears the same title. This fact sheet presents an abbreviated guide for designing and implementing solvent extraction treatability studies. The fact sheet presents a description of and discusses the applicability and limitations of solvent extraction technologies and defines the prescreening and field measurement data needed to determine if treatability testing is required.

  1. The treatable intellectual disability APP www.treatable-id.org: A digital tool to enhance diagnosis & care for rare diseases

    PubMed Central

    2012-01-01

    Background Intellectual disability (ID) is a devastating and frequent condition, affecting 2-3% of the population worldwide. Early recognition of treatable underlying conditions drastically improves health outcomes and decreases burdens to patients, families and society. Our systematic literature review identified 81 such inborn errors of metabolism, which present with ID as a prominent feature and are amenable to causal therapy. The WebAPP translates this knowledge of rare diseases into a diagnostic tool and information portal. Methods & results Freely available as a WebAPP via http://www.treatable-id.org and end 2012 via the APP store, this diagnostic tool is designed for all specialists evaluating children with global delay / ID and laboratory scientists. Information on the 81 diseases is presented in different ways with search functions: 15 biochemical categories, neurologic and non-neurologic signs & symptoms, diagnostic investigations (metabolic screening tests in blood and urine identify 65% of all IEM), therapies & effects on primary (IQ/developmental quotient) and secondary outcomes, and available evidence For each rare condition a ‘disease page’ serves as an information portal with online access to specific genetics, biochemistry, phenotype, diagnostic tests and therapeutic options. As new knowledge and evidence is gained from expert input and PubMed searches this tool will be continually updated. The WebAPP is an integral part of a protocol prioritizing treatability in the work-up of every child with global delay / ID. A 3-year funded study will enable an evaluation of its effectiveness. Conclusions For rare diseases, a field for which financial and scientific resources are particularly scarce, knowledge translation challenges are abundant. With this WebAPP technology is capitalized to raise awareness for rare treatable diseases and their common presenting clinical feature of ID, with the potential to improve health outcomes. This innovative digital

  2. Neutron Diffraction Studies of Carbonate Apatite

    NASA Astrophysics Data System (ADS)

    Moghaddam, Hadi Y.; Leventouri, Theodora; Chakoumakos, Bryan C.

    1998-11-01

    Moghaddam H.Y., Leventouri Th.* (Dept. of Physics & Alloy Research Center, Florida Atlantic Univ.) Chakoumakos B.C. (Solid State Division, Oak Ridge National Lab.**,kou@ornl.gov) We report Rietveld structural refinements of neutron diffraction data of a highly crystalline, single-phase natural carbonate apatite,(francolite of Epirus, Greece), in order to elucidate the details of carbonate substitution in the apatites. The composition is Ca9.56Na0.38Mg0.08(PO4)4.82(CO3)0.946(SO4)0.2F2.34, as determined by electron microprobe analysis. We report refinements of data for the native francolite as a function of temperature between 296K and 10K after the material had been heated at 750 °C to drive off adsorbed water and CO2. The neutron diffractioii@data were collected using a wavelength 1.0912 A on the HB4 high resolution powder diffractometer at the High Flux Isotope Reactor at Oak Ridge National Laboratory. Analysis of the temperature dependence of the anisotropic displacement parameters can reveal the contribution from the temperature independent static positional disorder. Difference displacement parameters evaluated along various bonding directions are being used to describe the mechanics and dynamics of the carbonate for phosphate substitution.*Supported by a SURA-ORNL Summer Cooperative Research Program 1998.**Supported by the Division of Materials Sciences,U.S. D.O.E. (contract DE-AC05-96OR22464 with Lockheed Martin Energy Research Corporation).

  3. Immobilization of uranium in contaminated soil by natural apatite addition

    SciTech Connect

    Mrdakovic Popic, Jelena; Stojanovic, Mirjana; Milosevic, Sinisa; Iles, Deana; Zildzovic, Snezana

    2007-07-01

    Available in abstract form only. Full text of publication follows: The goal of this study was to evaluate the effectiveness of Serbian natural mineral apatite as soil additive for reducing the migration of uranium from contaminated sediments. In laboratory study we investigated the sorption properties of domestic apatite upon different experimental conditions, such as pH, adsorbent mass, reaction period, concentration of P{sub 2}O{sub 5} in apatite, solid/liquid ratio. In second part of study, we did the quantification of uranium in soil samples, taken from uranium mine site 'Kalna', by sequential extraction method. The same procedure was, also, used for uranium determination in contaminated soil samples after apatite addition, in order to determine the changes in U distribution in soil fraction. The obtained results showed the significant level of immobilization (96.7%) upon certain conditions. Increase of %P{sub 2}O{sub 5} in apatite and process of mechano-chemical activation led to increase of immobilization capacity from 17.50% till 91.64%. The best results for uranium binding were obtained at pH 5.5 and reaction period 60 days (98.04%) The sequential extraction showed the presence of uranium (48.2%) in potentially available soil fractions, but with the apatite addition uranium content in these fractions decreased (30.64%), what is considering environmental aspect significant fact. In situ immobilization of radionuclide using inexpensive sequestering agents, such as apatite, is very adequate for big contaminated areas of soil with low level of contamination. This investigation study on natural apatite from deposit 'Lisina' Serbia was the first one of this type in our country. Key words: apatite, uranium, immobilization, soil, contamination. (authors)

  4. UV photofunctionalization promotes nano-biomimetic apatite deposition on titanium

    PubMed Central

    Saita, Makiko; Ikeda, Takayuki; Yamada, Masahiro; Kimoto, Katsuhiko; Lee, Masaichi Chang-Il; Ogawa, Takahiro

    2016-01-01

    Background Although biomimetic apatite coating is a promising way to provide titanium with osteoconductivity, the efficiency and quality of deposition is often poor. Most titanium implants have microscale surface morphology, and an addition of nanoscale features while preserving the micromorphology may provide further biological benefit. Here, we examined the effect of ultraviolet (UV) light treatment of titanium, or photofunctionalization, on the efficacy of biomimetic apatite deposition on titanium and its biological capability. Methods and results Micro-roughed titanium disks were prepared by acid-etching with sulfuric acid. Micro-roughened disks with or without photofunctionalization (20-minute exposure to UV light) were immersed in simulated body fluid (SBF) for 1 or 5 days. Photofunctionalized titanium disks were superhydrophilic and did not form surface air bubbles when immersed in SBF, whereas non-photofunctionalized disks were hydrophobic and largely covered with air bubbles during immersion. An apatite-related signal was observed by X-ray diffraction on photofunctionalized titanium after 1 day of SBF immersion, which was equivalent to the one observed after 5 days of immersion of control titanium. Scanning electron microscopy revealed nodular apatite deposition in the valleys and at the inclines of micro-roughened structures without affecting the existing micro-configuration. Micro-roughened titanium and apatite-deposited titanium surfaces had similar roughness values. The attachment, spreading, settling, proliferation, and alkaline phosphate activity of bone marrow-derived osteoblasts were promoted on apatite-coated titanium with photofunctionalization. Conclusion UV-photofunctionalization of titanium enabled faster deposition of nanoscale biomimetic apatite, resulting in the improved biological capability compared to the similarly prepared apatite-deposited titanium without photofunctionalization. Photofunctionalization-assisted biomimetic apatite

  5. [Treatable Dementia due to Vitamin B12 and Folate Deficiency].

    PubMed

    Yoshizawa, Toshihiro

    2016-04-01

    Vitamin deficiency is one of the major causes of treatable dementia. Specifically, patients suffering from dementia frequentry display low serum levels of vitamin B(12). There is a close metabolic interaction between folate and vitamin B(12). Folate deficiency causes various neuropsychiatric symptoms, which resemble those observed in vitamin B(12) deficiency. This review summarizes, the basic pathophysiology of vitamin B(12) and folate deficiency, its clinical diagnosis, associated neuropsychiatric symptoms such as subacute combined degeneration and dementia, and epidemiological studies of cognitive decline and brain atrophy. PMID:27056859

  6. Miscellaneous chemical basin treatability study: an analysis of passive soil vapor extraction wells (PSVE)

    SciTech Connect

    Riha, B.; Rossabi, J.

    1997-12-01

    A passive soil vapor extraction (PSVE) treatability study at the Miscellaneous Chemical Basin (MCB) of the Savannah River Site (SRS) has been progressing since September 1996. The results to date on the treatability study of the PSVE system indicate that the technology is performing well.

  7. Process and equipment development for hot isostatic pressing treatability study

    SciTech Connect

    Bateman, Ken; Wahlquist, Dennis; Malewitz, Tim

    2015-03-01

    Battelle Energy Alliance (BEA), LLC, has developed processes and equipment for a pilot-scale hot isostatic pressing (HIP) treatability study to stabilize and volume reduce radioactive calcine stored at Idaho National Laboratory (INL). In 2009, the U. S. Department of Energy signed a Record of Decision with the state of Idaho selecting HIP technology as the method to treat 5,800 yd^3 (4,400 m^3) of granular zirconia and alumina calcine produced between 1953 and 1992 as a waste byproduct of spent nuclear fuel reprocessing. Since the 1990s, a variety of radioactive and hazardous waste forms have been remotely treated using HIP within INL hot cells. To execute the remote process at INL, waste is loaded into a stainless-steel or aluminum can, which is evacuated, sealed, and placed into a HIP furnace. The HIP simultaneously heats and pressurizes the waste, reducing its volume and increasing its durability. Two 1 gal cans of calcine waste currently stored in a shielded cask were identified as candidate materials for a treatability study involving the HIP process. Equipment and materials for cask-handling and calcine transfer into INL hot cells, as well as remotely operated equipment for waste can opening, particle sizing, material blending, and HIP can loading have been designed and successfully tested. These results demonstrate BEA’s readiness for treatment of INL calcine.

  8. Hydrated lime for metals immobilization and explosives transformation: Treatability study.

    PubMed

    Martin, W Andy; Larson, S L; Nestler, C C; Fabian, G; O'Connor, G; Felt, D R

    2012-05-15

    Fragmentation grenades contain Composition B (RDX and TNT) within a steel shell casing. There is the potential for off-site migration of high explosives and metals from hand grenade training ranges by transport in surface water and subsurface transport in leachate. This treatability study used bench-scale columns and mesocosm-scale laboratory lysimeters to investigate the potential of hydrated lime as a soil amendment for in situ remediation of explosives and metals stabilization in hand grenade range soils. Compared to the unamended soil there was a 26-92% reduction of RDX in the leachate and runoff water from the lime treated soils and a 66-83% reduction of zinc in the leachate and runoff water samples; where the hand grenade range metals of concern were zinc, iron, and manganese. The amended soil was maintained at the target pH of greater than 10.5 for optimum explosives decomposition. The treatability study indicated a high potential of success for scale-up to an in situ field study. PMID:22445717

  9. Hanford 100-D Area Biostimulation Treatability Test Results

    SciTech Connect

    Truex, Michael J.; Vermeul, Vincent R.; Fritz, Brad G.; Mackley, Rob D.; Mendoza, Donaldo P.; Elmore, Rebecca P.; Mitroshkov, Alexandre V.; Sklarew, Deborah S.; Johnson, Christian D.; Oostrom, Martinus; Newcomer, Darrell R.; Brockman, Fred J.; Bilskis, Christina L.; Hubbard, Susan S.; Peterson, John E.; Williams, Kenneth H.; Gasperikova, E.; Ajo-Franklin, J.

    2009-09-30

    Pacific Northwest National Laboratory conducted a treatability test designed to demonstrate that in situ biostimulation can be applied to help meet cleanup goals in the Hanford Site 100-D Area. In situ biostimulation has been extensively researched and applied for aquifer remediation over the last 20 years for various contaminants. In situ biostimulation, in the context of this project, is the process of amending an aquifer with a substrate that induces growth and/or activity of indigenous bacteria for the purpose of inducing a desired reaction. For application at the 100-D Area, the purpose of biostimulation is to induce reduction of chromate, nitrate, and oxygen to remove these compounds from the groundwater. The in situ biostimulation technology is intended to provide supplemental treatment upgradient of the In Situ Redox Manipulation (ISRM) barrier previously installed in the Hanford 100-D Area and thereby increase the longevity of the ISRM barrier. Substrates for the treatability test were selected to provide information about two general approaches for establishing and maintaining an in situ permeable reactive barrier based on biological reactions, i.e., a biobarrier. These approaches included 1) use of a soluble (miscible) substrate that is relatively easy to distribute over a large areal extent, is inexpensive, and is expected to have moderate longevity; and 2) use of an immiscible substrate that can be distributed over a reasonable areal extent at a moderate cost and is expected to have increased longevity.

  10. Insight into Biological Apatite: Physiochemical Properties and Preparation Approaches

    PubMed Central

    Liu, Quan; Matinlinna, Jukka Pekka; Chen, Zhuofan; Pan, Haobo

    2013-01-01

    Biological apatite is an inorganic calcium phosphate salt in apatite form and nano size with a biological derivation. It is also the main inorganic component of biological hard tissues such as bones and teeth of vertebrates. Consequently, biological apatite has a wide application in dentistry and orthopedics by using as dental fillers and bone substitutes for bone reconstruction and regeneration. Given this, it is of great significance to obtain a comprehensive understanding of its physiochemical and biological properties. However, upon the previous studies, inconsistent and inadequate data of such basic properties as the morphology, crystal size, chemical compositions, and solubility of biological apatite were reported. This may be ascribed to the differences in the source of raw materials that biological apatite are made from, as well as the effect of the preparation approaches. Hence, this paper is to provide some insights rather than a thorough review of the physiochemical properties as well as the advantages and drawbacks of various preparation methods of biological apatite. PMID:24078928

  11. Apatite mineralization in elasmobranch skeletons via a polyphosphate intermediate

    NASA Astrophysics Data System (ADS)

    Omelon, Sidney; Lacroix, Nicolas; Lildhar, Levannia; Variola, Fabio; Dean, Mason

    2014-05-01

    All vertebrate skeletons are stiffened with apatite, a calcium phosphate mineral. Control of apatite mineralization is essential to the growth and repair of the biology of these skeletons, ensuring that apatite is deposited in the correct tissue location at the desired time. The mechanism of this biochemical control remains debated, but must involve increasing the localized apatite saturation state. It was theorized in 1923 that alkaline phosphatase (ALP) activity provides this control mechanism by increasing the inorganic phosphate (Pi) concentration via dephosphorylation of phosphorylated molecules. The ALP substrate for biological apatite is not known. We propose that polyphosphates (polyPs) produced by mitochondria may be the substrate for biological apatite formation by ALP activity. PolyPs (PO3-)n, also known as condensed phosphates, represent a concentrated, bioavailable Pi-storage strategy. Mitochondria import Pi and synthesize phosphate polymers through an unknown biochemical mechanism. When chelated with calcium and/or other cations, the effective P-concentration of these neutrally charged, amorphous, polyP species can be very high (~ 0.5 M), without inducing phosphate mineral crystallization. This P-concentration in the low Pi-concentration biological environment offers a method of concentrating P well above an apatite supersaturation required for nucleation. Bone is the most studied mineralized skeletal tissue. However, locating and analyzing active mineralizing areas is challenging. We studied calcified cartilage skeletons of elasmobranch fishes (sharks, stingrays and relatives) to analyse the phosphate chemistry in this continually mineralizing skeleton. Although the majority of the elasmobranch skeleton is unmineralized cartilage, it is wrapped in an outer layer of mineralized tissue comprised of small tiles called tesserae. These calcified tesserae continually grow through the formation of new mineral on their borders. Co-localization of ALP and

  12. Transformation of apatite phosphorus and non-apatite inorganic phosphorus during incineration of sewage sludge.

    PubMed

    Li, Rundong; Zhang, Ziheng; Li, Yanlong; Teng, Wenchao; Wang, Weiyun; Yang, Tianhua

    2015-12-01

    The recovery of phosphorus from incinerated sewage sludge ash (SSA) is assumed to be economical. Transformation from non-apatite inorganic phosphorus (NAIP) to apatite phosphorus (AP), which has a higher bioavailability and more extensive industrial applications, was studied at 750-950°C by sewage sludge incineration and model compound incineration with a calcium oxide (CaO) additive. Thermogravimetric differential scanning calorimetry analysis and X-ray diffraction measurements were used to analyze the reactions between NAIP with CaO and crystallized phases in SSA. High temperatures stimulated the volatilization of NAIP instead of AP. Sewage sludge incineration with CaO transformed NAIP into AP, and the percentage of AP from the total phosphorus reached 99% at 950°C. Aluminum phosphate reacted with CaO, forming Ca2P2O7 and Ca3(PO4)2 at 750-950°C. Reactions between iron phosphate and CaO occurred at lower temperatures, forming Ca(PO3)2 before reaching 850°C. PMID:26113414

  13. Treatability study of pesticide-based industrial wastewater.

    PubMed

    Shah, Kinnari; Chauhan, L I; Galgale, A D

    2012-10-01

    This paper finds out appropriate treatment methods for wastewater of an Organophosphorus viz, chloropyrifos pesticide manufacturing industry. The characterization of wastewater generated during trial production of chloropyrifos was carried out. Based on the characterization of wastewater, various treatability studies were conducted. The most desirable results were obtained with treatment scheme employing acidification, chlorination with NaOCl, suspended growth biological treatment, chemical precipitation for phosphorous removal and activated carbon treatment. Acidification of wastewater helps in by-product recovery as well as reduction in COD upto 36.26%. Chlorination followed by biological treatment was found to be effective to reduce the COD level by 62.06%. To comply with permissible limits prescribed by Effluent Channel Project Ltd.(ECPL)* and Gujarat Pollution Control Board (GPCB) for discharge of industrial effluent into channel, further treatment in the form of chemical precipitation (for phosphorous removal) and granular activated carbon is suggested. PMID:25151721

  14. Apatite accumulation enhances the mechanical property of anammox granules.

    PubMed

    Lin, Y M; Lotti, T; Sharma, P K; van Loosdrecht, M C M

    2013-09-01

    The strength of granular sludge is essential for the mechanical stability of the granules. Inorganic precipitants form a major factor influencing the strength of the granules. To check the possibility of apatite accumulation in anammox granules, and study its contribution to the mechanical strength of granules, anammox granular sludge was collected from Dokhaven municipal wastewater treatment plant, the Netherlands. Mineral precipitation inside the granules was visualized by micro-computed tomography, and apatite was identified by electron probe microanalysis and X-ray powder diffraction. The mechanical strength of anammox granules was measured by a low load compression tester. The contribution of apatite to the mechanical strength was evaluated by the generalized Maxwell model. Ca-PO4 minerals are reported to accumulate in anammox granules. A transformation of Ca-PO4 happens, and apatite is the final stable form. The accumulation of apatite increases the mechanical strength of anammox granules. A fast method to monitor and evaluate the accumulation of minerals in anammox granules was proposed. PMID:23764605

  15. Tissue response of apatite-filled resin cement and titanium-reinforced apatite dental implants in dogs.

    PubMed

    Ogiso, M; Tabata, T; Nakabayashi, N; Yamashita, Y; Borgese, D

    1993-01-01

    Abutment and root portion divided two-piece dental implants were designed to modify the one-piece dense hydroxyapatite (D-HAP) implant. The initial placement of the root portion endosseously ensured an aseptic environment and physical stability for the implant during the bone healing period. The outer D-HAP shell of the root portion was fortified by an inner titanium cylinder and cemented with an adhesive resin cement containing 4-methacryloyoxyethyl trimellitate anhydride (4-META) and reinforced by fine apatite filler. Upon attaining integration of the bone and implant, the abutment was screwed and fixed into the screw hole of the root portion. The tissue response of both the apatite-filled resin cement and root portion of the two-piece implant was studied by animal canine experiments. Light and electron microscopic examination of specimens taken from experimental animal tissue showed bone contacted directly not only the exposed apatite filler at the surface of the apatite-filled resin cement, but also the resin portion. These findings of direct bone contact suggested that the tissue response of apatite-filled resin cement was approximately similar to the usual D-HAP. Because most of the surface of the outer D-HAP shell of the root portion came in contact with bone, it prevented the deposition of contamination on the D-HAP surface during the manufacturing procedures of the root portion. PMID:10148567

  16. Tetracycline-loaded biomimetic apatite: an adsorption study.

    PubMed

    Cazalbou, Sophie; Bertrand, Ghislaine; Drouet, Christophe

    2015-02-19

    Biomimetic apatites are appealing compounds for the elaboration of bioactive bone-repair scaffolds due to their intrinsic similarity to bone mineral. Bone surgeries are however often heavy procedures, and the infiltration of pathogens may not be totally avoided. To prevent their development, systemic antibiotic prophylaxis is widespread but does not specifically target surgical sites and involves doses not always optimized. A relevant alternative is a preliminary functionalization by an infection-fighting agent. In this work, we investigated from a physicochemical viewpoint the association of a wide-spectrum antibiotic, tetracycline (TC), and a biomimetic nanocrystalline apatite previously characterized. TC adsorption kinetics and isotherm were thoroughly explored. Kinetic data were fitted to various models (pseudo-first-order, pseudo-second-order, general kinetic model of order n, Elovich, double-exponential, and purely diffusive models). The best fit was found for a double-exponential kinetic model or with a decimal reaction order of 1.4, highlighting a complex process with such TC molecules which do not expose high-affinity end groups for the surface of apatite. The adsorption isotherm was perfectly fitted to the Sips (Langmuir-Freundlich) model, while other models failed to describe it, and the Sips exponent greater than unity (1.08) suggested a joint impact of surface heterogeneity and positive cooperativity between adsorbed molecules. Finally, preliminary insights on TC release from pelletized nanocrystalline apatite, in aqueous medium and neutral pH, were obtained using a recirculation cell, indicating a release profile mainly following a Higuchi-like diffusion-limited rate. This work is intended to shed more light on the interaction between polar molecules not exhibiting high-affinity end groups and biomimetic apatites and is a starting point in view of the elaboration of biomimetic apatite-based bone scaffolds functionalized with polar organic drugs for a

  17. Characterization, physicochemical properties and biocompatibility of La-incorporated apatites.

    PubMed

    Guo, D G; Wang, A H; Han, Y; Xu, K W

    2009-11-01

    In this study, the physicochemical properties and biocompatibilities of La-containing apatites were intensively investigated together with their characterizations in terms of composition, structure, valent state and morphology using X-ray diffraction, Fourier-transform infrared spectra, X-ray photoelectron spectroscopy, scanning electron microscopy and energy dispersive X-ray spectroscopy, respectively. The results indicate that the La(3+) ion can be incorporated into the crystal lattice of hydroxyapatite resulting in the production of La-incorporated apatites (La(x)Ca(10-x)(PO(4))(6)(OH)(2+x-2y)O(y square y-x) (x> or =0.5, y<1+x/2) or La(x)Ca(10-x)(PO(4))(6)O(y square y-x) (0.5apatites. In contrast to La-free apatite, La-incorporated apatites possess a series of attractive properties, including higher thermal stability, higher flexural strength, lower dissolution rate, larger alkaline phosphatase activity, preferable osteoblast morphology and comparable cytotoxicity. In particular, the sintered La-incorporated apatite block achieves a maximal flexure strength of 66.69+/-0.98 MPa at 5% La content (confidence coefficient 0.95), increased 320% in comparison with the La-free apatite. The present study suggests that the La-incorporated apatite possesses application potential in developing a new type of bioactive coating material for metal implants and also as a promising La carrier for further exploring the beneficial functions of La in the human body. PMID:19477306

  18. Calibration for Infrared Measurements of OH in Apatite

    NASA Astrophysics Data System (ADS)

    Wang, K. L.; Naab, F.; Zhang, Y.

    2010-12-01

    Apatite is a common accessory mineral, and OH in apatite can indicate the fluid conditions of crystal formation. Previously, water (OH) concentration in apatite has often been estimated through electron microprobe analyses combined with mineral stoichiometry. However, the detection limit, precision, and accuracy of this method are not high. In this work, we calibrated the infrared spectroscopy (IR) method for measurement of OH concentration in apatite by using elastic recoil detection (ERD) analysis to obtain the absolute OH concentration. Large apatite wafers were cut perpendicular to the c-axis of each crystal and doubly polished. ERD measurements were carried out in the Michigan Ion Beam Laboratory at the University of Michigan to determine the hydrogen concentration in each sample. Each ERD spectrum was fitted and a hydrogen standard was used to quantify the hydrogen concentrations. Polarized transmission IR was used on apatite sections that were cut parallel to the c-axis, and doubly polished. IR measurements were made for E-vector parallel to the c-axis. Because the OH peak is intense, very thin samples must be used to avoid absorbance saturation; the thinnest sample (corresponding to the highest OH content) used was 17 µm thick. Four different apatite crystals were successfully analyzed using both the IR and ERD methods. Two were from Durango, Mexico; one from Imilchil, High Atlas Mountains, Morocco; and one from an unknown locality, purchased online from gem dealers. The OH peak near 3550 cm-1 was a relatively simple peak in all four samples. Therefore peak height was used for the absorbance value, A. Using the Beer-Lambert Law, a calibration line was established (R2= 0.95, for IR aperture of 50 µm x 50 µm) where the weight % of H2O is 0.013 times A/d, where d is the thickness in mm. The detection limit of H2O concentration in apatite by IR approaches ppm level for 0.1 mm wafers, the precision is better than 1% relative (depending on H2O content), and

  19. Composition dependent thermal annealing behaviour of ion tracks in apatite

    NASA Astrophysics Data System (ADS)

    Nadzri, A.; Schauries, D.; Mota-Santiago, P.; Muradoglu, S.; Trautmann, C.; Gleadow, A. J. W.; Hawley, A.; Kluth, P.

    2016-07-01

    Natural apatite samples with different F/Cl content from a variety of geological locations (Durango, Mexico; Mud Tank, Australia; and Snarum, Norway) were irradiated with swift heavy ions to simulate fission tracks. The annealing kinetics of the resulting ion tracks was investigated using synchrotron-based small-angle X-ray scattering (SAXS) combined with ex situ annealing. The activation energies for track recrystallization were extracted and consistent with previous studies using track-etching, tracks in the chlorine-rich Snarum apatite are more resistant to annealing than in the other compositions.

  20. SUMMARY PLAN FOR BENCH-SCALE REFORMER AND PRODUCT TESTING TREATABILITY STUDIES USING HANFORD TANK WASTE

    SciTech Connect

    ROBBINS RA

    2011-02-11

    This paper describes the sample selection, sample preparation, environmental, and regulatory considerations for shipment of Hanford radioactive waste samples for treatability studies of the FBSR process at the Savannah River National Laboratory and the Pacific Northwest National Laboratory.

  1. LOGAN WASH FIELD TREATABILITY STUDIES OF WASTEWATERS FROM OIL SHALE RETORTING PROCESSES

    EPA Science Inventory

    Treatability studies were conducted on retort water and gas condensate wastewater from modified in-situ oil shale retorts to evaluate the effectiveness of selected treatment technologies for removing organic and inorganic contaminants. At retorts operated by Occidental Oil Shale,...

  2. TOXICITY TREATABILITY OF IRON AND STEEL PLANT WASTEWATERS: A RESOURCE DOCUMENT

    EPA Science Inventory

    The report gives results of an assessment of the toxicity treatability of wastewaters from eight steelmaking subcategories, all considered assessable under the somewhat low production levels of the study period. Tests were conducted using prescribed procedures for conventional wa...

  3. GUIDE FOR CONDUCTING TREATABILITY STUDIES UNDER CERCLA: THERMAL DESORPTION - INTERIM GUIDANCE

    EPA Science Inventory

    Systematically conducted, well-documented treatability studies are an important component of the remedial investigation/feasibility study (RI/FS) process and the remedial design remedial action (RD/RA) process under the Comprehensive Environmental Response, Compensation, and Liab...

  4. GUIDE FOR CONDUCTING TREATABILITY STUDIES UNDER CERCLA: AEROBIC BIODEGRADATION REMEDY SCREENING

    EPA Science Inventory

    Systematically conducted, well-documented treatability studies are an important component of the remedial investigation/feasibility study (KU FS) process and the remedial design/remedial action (RD/RA) process under the Comprehensive Environmental Response, Compensation, and L...

  5. EPA’s Drinking Water Treatability Database: A Tool for All Drinking Water Professionals

    EPA Science Inventory

    The Drinking Water Treatability Database (TDB) is being developed by the USEPA Office of Research and Development to allow drinking water professionals and others to access referenced information gathered from thousands of literature sources and assembled on one site. Currently, ...

  6. Carbon and oxygen isotopes in apatite CO/sub 2/ and co-existing calcite

    SciTech Connect

    Kolodny, Y.; Kaplan, I. R.

    1981-04-01

    Carbon and oxygen isotopes were analyzed in carbonate apatite CO/sub 2/ and in co-existing calcite. Both C and O in apatite CO/sub 2/ are enriched in the respective light isotopes relative to calcite. These results confirm the proposition that carbonate is part of the apatite structure.

  7. Treatability study Number PDC-1-O-T. Final report

    SciTech Connect

    1998-04-22

    Los Alamos National Laboratory provided treatability study samples from four waste streams, designated Stream {number_sign}1, Stream {number_sign}3, Stream {number_sign}6, and Stream {number_sign}7. Stream {number_sign}1 consisted of one 55-gallon drum of personal protective equipment (PPE), rags, and neutralizing agent (bicarbonate) generated during the cleanup of a sodium dichromate solution spill. Stream {number_sign}3 was one 55-gallon drum of paper, rags, lab utensils, tools, and tape from the decontamination of a glovebox. The sample of Stream {number_sign}6 was packaged in three 30-gallon drums and a 100 ft{sup 3} wooden box. It consisted of plastic sheeting, PPE, and paper generated from the cleanup of mock explosive (barium nitrate) from depleted uranium parts. Stream {number_sign}7 was scrap metal (copper, stainless and carbon steel joined with silver solder) from the disassembly of gas manifolds. The objective of the treatability study is to determine: (1) whether the Perma-Fix stabilization/solidification process can treat the waste sample to meet Land Disposal Restrictions and the Waste Acceptance Criteria for LANL Technical Area 54, Area G, and (2) optimum loading and resulting weight and volume of finished waste form. The stabilized waste was mixed into grout that had been poured into a lined drum. After each original container of waste was processed, the liner was closed and a new liner was placed in the same drum on top of the previous closed liner. This allowed an overall reduction in waste volume but kept waste segregated to minimize the amount of rework in case analytical results indicated any batch did not meet treatment standards. Samples of treated waste from each waste stream were analyzed by Perma-Fix Analytical Services to get a preliminary approximation of TCLP metals. Splits of these samples were sent to American Environmental Network`s mixed waste analytical lab in Cary, NC for confirmation analysis. Results were all below applicable

  8. Ultrastructural observation of single-crystal apatite fibres.

    PubMed

    Aizawa, Mamoru; Porter, Alexandra E; Best, Serena M; Bonfield, William

    2005-06-01

    Hydroxyapatite (HAp) has been widely used as a biomaterial for substituting human hard tissues such as bone. By altering the morphology of HAp crystals, novel properties may be produced by controlling the orientation of the crystal planes. Apatite fibres were successfully synthesized by precipitation from aqueous solutions containing Ca(NO(3))(2), (NH(4))(2)HPO(4), urea and HNO(3). The products were composed of carbonate-containing apatite fibres with preferred orientation along the {h00} planes. Examination of individual fibres using transmission electron microscopy showed that the as-synthesized apatite fibres were highly strained single crystals with the c-axis orientation parallel to the long axis of the fibre. The crushed fibres consisted of domains that were preferentially oriented with the c-axis parallel to the long axis of the fibres. When the apatite fibres were heated to 800, 1000 and 1200 degrees C for 1h, the domains were removed and grain boundaries, dislocations and voids were formed. PMID:15621231

  9. Apatite as a paleohydrothermal fluid recorder in Carlin-type gold deposits

    NASA Astrophysics Data System (ADS)

    Barker, S. L.; Hickey, K. A.; Dipple, G. M.; Layne, G.

    2009-05-01

    Apatite is a common accessory mineral in most rocks. A variety of trace elements can be substituted into apatite, meaning that apatite has the potential to record changes in the chemistry of ore-forming hydrothermal fluids. This study focuses on variations in apatite texture and chemistry around the world-class Carlin-type Au deposits of NE Nevada. These deposits are characterized by cryptic alteration of calcareous and siliciclastic sedimentary rocks induced by acidic, low-temperature (150-220 °C) ore fluids. A large database of apatite fission track (AFT) samples collected from NE Nevada (Hickey, unpublished data) is being used to examine relationships between apatite fission track ages, textural zonation within apatite crystals and apatite trace element composition. AFT data from "background" samples collected away from hydrothermal mineralization and Cenozoic igneous stocks reveal that regional uplift occurred in the Cretaceous at ~70-60 Ma. In comparison, AFT data from samples around gold mineralization reveal an Eocene heating event, interpreted as the result of hydrothermal reheating by the Carlin Au-forming system (Cline et al., 2005). Optical cathodoluminescence observations reveal that some apatite from Au-bearing material (Eocene AFT age) has embayed cores, and at least four generations of overgrowths (typically ˜10 μm wide overgrowths), which may also be embayed. In comparison, apatite from hydrothermally altered, but unmineralized, material has a single overgrowth generation. 'Background' apatites do not have significant overgrowths. Current research is characterizing the trace element composition of apatite cores and overgrowths via SIMS. We propose that apatite textures and trace element composition record hydrothermal fluid interactions. Applications include using apatite to detect the signature of hydrothermal fluids in rocks cryptically altered by low-temperature hydrothermal systems, or detecting mineralization by examining detrital apatites

  10. Apatite: a new redox proxy for silicic magmas?

    NASA Astrophysics Data System (ADS)

    Miles, Andrew; Graham, Colin; Hawkesworth, Chris; Gillespie, Martin; Bromiley, Geoff; Hinton, Richard

    2015-04-01

    The oxidation states of magmas provide valuable information about the release and speciation of volatile elements during volcanic eruptions, metallogenesis, source rock compositions, open system magmatic processes, tectonic settings and potentially titanium (Ti) activity in chemical systems used for Ti-dependent geothermometers and geobarometers. In this presentation we explore the use of Mn in apatite as an oxybarometer in intermediate and silicic igneous rocks. Increased Mn concentrations in apatite in granitic rocks from the zoned Criffell granitic pluton (southern Scotland) correlate with decreasing Fe2O3 (Fe3+) and Mn in the whole-rock and likely reflect increased Mn2+/Mn3+and greater compatibility of Mn2+ relative to Mn3+ in apatite under reduced conditions. Fe3+/Fe2+ ratios in biotites have previously been used to calculate oxygen fugacities (fO2) in the outer zone granodiorites and inner zone granites where redox conditions have been shown to change from close to the magnetite-hematite buffer to close to the nickel-nickel oxide buffer respectively[1]. This trend is apparent in apatite Mn concentrations from a range of intermediate to silicic volcanic rocks that exhibit varying redox states and are shown to vary linearly and negatively with log fO2, such that logfO2=-0.0022(±0.0003)Mn(ppm)-9.75(±0.46) Variations in the Mn concentration of apatites appear to be largely independent of differences in the Mn concentration of the melt. Apatite Mn concentrations may therefore provide an independent oxybarometer that is amenable to experimental calibration, with major relevance to studies on detrital mineral suites, particularly those containing a record of early Earth redox conditions, and on the climatic impact of historic volcanic eruptions[2]. [1] Stephens, W. E., Whitley, J. E., Thirlwall, M. F. and Halliday, A. N. (1985) The Criffell zoned pluton: correlated behaviour of rare earth element abundances with isotopic systems. Contributions to Mineralogy and

  11. Firm contracts for treatability tests on contaminated soils

    SciTech Connect

    Not Available

    1989-08-01

    Geosafe Corporation, a Pacific Northwest-headquartered hazardous waste remediation company, announced that is has successfully completed treatability testing of contaminated soils under contract with Woodward Clyde Consultants of Denver, Colorado, the prime contractor for a major hazardous waste site in the Western United States. The tests are being conducted at the University of Washington with Geosafe's specially-designed test equipment. The recently concluded testing confirms the ability of Geosafe's patented in situ vitrification (ISV) technology to treat soils containing a variety of organic and inorganic contaminants. ISV, for which Geosafe has worldwide rights, is the only technology available today that will fully comply with the Superfund Amendments and Reauthorization Act. The ability of ISV to treat mixtures of organic, inorganic and radioactive wastes in situ, in a single process, offers distinct advantages over excavation, transportation and incineration. During the ISV process, organic contaminants are pyrolized and the inorganics present are chemically incorporated into the molten soil which, when cooled, resembles naturally-occurring obsidian.

  12. [Episacral lipoma: a treatable cause of low back pain].

    PubMed

    Erdem, Hatice Rana; Nacır, Barış; Özeri, Zuhal; Karagöz, Aynur

    2013-01-01

    Episacral lipoma is a small, tender subcutaneous nodule primarily occurring over the posterior iliac crest. Episacral lipoma is a significant and treatable cause of acute and chronic low back pain. Episacral lipoma occurs as a result of tears in the thoracodorsal fascia and subsequent herniation of a portion of the underlying dorsal fat pad through the tear. This clinical entity is common, and recognition is simple. The presence of a painful nodule with disappearance of pain after injection with anaesthetic, is diagnostic. Medication and physical therapy may not be effective. Local injection of the nodule with a solution of anaesthetic and steroid is effective in treating the episacral lipoma. Here we describe 2 patients with painful nodules over the posterior iliac crest. One patient complained of severe lower back pain radiating to the left lower extremity and this patient subsequently underwent disc operation. The other patient had been treated for greater trochanteric pain syndrome. In both patients, symptoms appeared to be relieved by local injection of anaesthetic and steroid. Episacral lipoma should be considered during diagnostic workup and in differential diagnosis of acute and chronic low back pain. PMID:23720083

  13. Treatability study for the stabilization of chromium contaminated waste

    SciTech Connect

    McGahan, J.F.; Martin, D.

    1994-12-31

    A process has been developed which immobilizes chromium in calcined uranyl nitrate mixed waste, resulting in a waste form disposable as radioactive, non hazardous waste. A prime contractor at the Idaho National Engineering Laboratory generates a radioactive waste contaminated with chromium. During handling, the waste becomes contaminated at a concentration sufficiently high to cause the waste to exceed the EPA`s Toxicity Characteristic Leaching Procedure (TCLP) leachable limit for chromium. A treatability test program was instigated to define the optimum conditions for the chemical reduction pretreatment step necessary for the stabilization of the contaminated waste. Sodium dithionite was determined to be the reducing agent of choice. A dithionite demand experiment was run to determine optimum dithionite dose. This dose, plus 67 percent excess, was added to each sample. Four different stabilization systems, at three different dosage levels, were investigated. The best performing reagent system was chosen for scale-up and more stringent performance testing. In one of the tested reagent systems, Portland cement sodium silicate and dithionite, all of the samples exhibited TCLP extract concentrations for chromium well below the regulatory limit. Portland cement/blast furnace slag blend had one passing sample, and for cement/fly ash and cement alone none of the samples had passing values for leachable chromium. The samples scaled-up passed the performance criteria and the process which is currently undergoing implementation at INEL has successfully converted mixed waste into radioactive waste for disposal.

  14. Solidifications/stabilization treatability study of a mixed waste sludge

    SciTech Connect

    Spence, R.D.; Stine, E.F.

    1996-03-01

    The Department of Energy Oak Ridge Operations Office signed a Federal Facility Compliance Agreement with the US Environmental Protection Agency Region IV regarding mixed wastes from the Oak Ridge Reservation (ORR) subject to the land disposal restriction provisions of the Resource Conservation and Recovery Act (RCRA). This agreement required treatability studies of solidification/stabilization (S/S) on mixed wastes from the ORR. This paper reports the results of the cementitious S/S studies conducted on a waste water treatment sludge generated from biodenitrification and heavy metals precipitation. For the cementitious waste forms, the additives tested were Portland cement, ground granulated blast furnace slag, Class F fly ash, and perlite. The properties measured on the treated waste were density, free-standing liquid, unconfined compressive strength, and TCLP performance. Spiking up to 10,000, 10,000, and 4,400 mg/kg of nickel, lead, and cadmium, respectively, was conducted to test waste composition variability and the stabilization limitations of the binding agents. The results indicated that nickel, lead and cadmium were stabilized fairly well in the high pH hydroxide-carbonate- ``bug bones`` sludge, but also clearly confirmed the established stabilization potential of cementitious S/S for these RCRA metals.

  15. [Treatable neurometabolic diseases. Association with schizophrenia spectrum disorders].

    PubMed

    Bonnot, Olivier; Herrera, Paula; Kuster, Alice

    2015-09-01

    Schizophrenia spectrum disorders are presented on 1% of subjects over general population. Organic pathologies prevalence in schizophrenia spectrum patients is not well determined, and it is probably underestimated. In the present update review, we are going to highlight seven treatable neurometabolic diseases (NMD) associated to sub-clinic neurological symptoms. It is not infrequent to witness the absence of any clinical neurological signs going along with the NMD. Psychiatric symptoms may be the only clinical alarm that can guide physicians to an acute diagnosis. This is why it is a challenging pathology, defying our clinical accuracy as psychiatrist or any other practitioners confronted to this population. Hereby we are going to expose a literature review and comprehensive tables in order to present in a glance the essential clinical features of disorders of homocysteine metabolism, urea cycle disorders, Niemann-Pick disease type C, acute porphyria, cerebrotendinous-xanthomatosis. These conditions are sensible to major improvement strongly correlated to the accuracy of diagnosis. Literature analysis led us to propose a comprehensive list of atypical psychiatric symptoms including highly predominant visual hallucinations, compared to auditory ones, as well as confusion, catatonia or progressive cognitive decline. We highlight the importance of considering antipsychotic treatment resistance as a crucial sign leading to suspect an organic factor beneath the psychiatric features. PMID:26248708

  16. SUPERFUND TREATABILITY CLEARINGHOUSE: ABSTRACT ON-SITE INCINERATION TESTING OF SHIRCO INFRARED SYSTEMS PORTABLE DEMONSTRATION UNIT-CONTAMINATED SOILS TREATABILITY STUDY

    EPA Science Inventory

    In August of 1986, Shirco was contracted by Dekonta GmbH, a Vest German hazardous waste treatment company, to perform treatability studies at one of the largest dioxin-contaminated sites in the world. The Shirco Infrared process was selected by Dekonta after a two year stud...

  17. SUPERFUND TREATABILITY CLEARINGHOUSE: BENGART AND MEMEL (BENCH-SCALE), GULFPORT (BENCH AND PILOT-SCALE), MONTANA POLE (BENCH-SCALE), AND WESTERN PROCESSING (BENCH-SCALE) TREATABILITY STUDIES

    EPA Science Inventory

    This document presents summary data on the results of various treatability studies (bench and pilot scale), conducted at three different sites where soils were contaminated with dioxins or PCBs. The synopsis is meant to show rough performance levels under a variety of differen...

  18. Dependence of ion concentration in simulated body fluid on apatite precipitation on titania surface

    NASA Astrophysics Data System (ADS)

    Sakaguchi, Akira; Nakano, Masayuki; Hieda, Junko; Ohtake, Naoto; Akasaka, Hiroki

    2015-08-01

    Titanium and its alloys are used as biomaterials, because of their high biocompatibility. Apatite precipitates on a titania surface in vivo, and living bone and titanium alloy are coupled through the thin apatite layer. The initial precipitation behavior of apatite on titania in simulated body fluid (SBF) solutions was evaluated and the effect of inorganic ions in the SBF was investigated. Measurement using the SPR phenomenon was used to evaluate the initial apatite precipitation. An SBF containing approximately equal ion concentrations to those in blood plasma was added to a titania surface and the SPR profile was obtained, from which the initial apatite precipitation rate was found to be 1.14 nm/h. Furthermore, the relationship between the inorganic concentration and the precipitation rate was determined for SBFs with different Na+ and Ca2+ concentrations. Apatite precipitation did not occur in the SBF with a low Na+ concentration, whereas the initial apatite precipitation rate in the SBF that did not contain Ca2+ was 0.32 nm/h. According to these results, Ca2+ has little effect on the initial apatite precipitation. In the initial reaction of apatite precipitation, sodium titanate is formed by the absorption of Na+. Next, calcium titanate precipitates upon the substitution of Na+ with Ca2+. Finally, Na+, phosphate ions and hydroxyl ions are attracted to the surface and apatite is formed. Thus, the rate-limiting factor in the initial nucleation of apatite is the Na+ concentration.

  19. Consideration of grain packing in granular iron treatability studies.

    PubMed

    Firdous, R; Devlin, J F

    2014-08-01

    Commercial granular iron (GI) is light steel that is used in Permeable Reactive Barriers (PRBs). Investigations into the reactivity of GI have focused on its chemical nature and relatively little direct work has been done to account for the effects of grain shape and packing. Both of these factors are expected to influence available grain surface area, which is known to correlate to reactivity. Commercial granular iron grains are platy and therefore pack in preferential orientations that could affect solution access to the surface. Three packing variations were investigated using Connelly Iron and trichloroethylene (TCE). Experimental kinetic data showed reaction rates 2-4 times higher when grains were packed with long axes preferentially parallel to flow (VP) compared to packings with long axes preferentially perpendicular to flow (HP) or randomly arranged (RP). The variations were found to be explainable by variations in reactive sorption capacities, i.e., sorption to sites where chemical transformations took place. The possibility that the different reactive sorption capacities were related to physical pore-scale differences was assessed by conducting an image analysis of the pore structure of sectioned columns. The analyses suggested that pore-scale factors - in particular the grain surface availability, reflected in the sorption capacity terms of the kinetic model used - could only account for a fraction of the observed reactivity differences between packing types. It is concluded that packing does affect observable reaction rates but that micro-scale features on the grain surfaces, rather than the pore scale characteristics, account for most of the apparent reactivity differences. This result suggests that treatability tests should consider the packing of columns carefully if they are to mimic field performance of PRBs to the greatest extent possible. PMID:25005796

  20. Treatability of chromite ore processing waste by leaching.

    PubMed

    Unlü, K; Haskök, S

    2001-06-01

    Developing treatment and disposal strategies and health-based clean-up standards for chromium containing wastes continues to be an important environmental regulatory issue because of the opposing solubility and toxicity characteristics of chromium species under diverse environmental conditions. In this study, leaching characteristics of total Cr and Cr(VI) were investigated using laboratory column studies. The data obtained from the experimental studies were analysed to assess the treatability of chromite ore processing waste (COPW) by leaching and to identify the leaching strategies that enhance mass removal rates of chromium species. COPW used for laboratory soil column studies was obtained from an industrial plant producing sodium chromate in Mersin, Turkey. Laboratory investigations involved chemical characterisation of waste material and column studies. For waste characterisation, U.S. EPA toxicity characterisation leaching procedure (TCLP) was performed on COPW to determine the concentrations of metal species in the TCLP extract. For column studies, various laboratory columns containing plain COPW material, 1:1 COPW/reducing agent (elemental iron or manure) mixture and different type soils (sand, loam and clay) overlain by COPW were subjected to leaching tests using acidic, neutral and alkaline influent water to determine Cr mass leaching efficiencies. Based on the TCLP analyses, COPW is classified as hazardous waste. As a result of comparing the leaching efficiency data from twelve leaching columns, the maximum removal of total Cr was achieved by leaching COPW/manure mixture using acidic (pH 4.78) influent water. The highest Cr(VI) leaching efficiency was achieved in the columns of plain COPW and COPW/manure mixture using highly alkaline (pH 12.0) influent water. The least effective leaching efficiency for both total Cr and Cr (VI) was obtained by leaching plain COPW with neutral (pH 7.0) influent water. Land-disposal of the treated COPW material by mixing

  1. Thermodynamic Mixing Behavior Of F-OH Apatite Crystalline Solutions

    NASA Astrophysics Data System (ADS)

    Hovis, G. L.

    2011-12-01

    It is important to establish a thermodynamic data base for accessory minerals and mineral series that are useful in determining fluid composition during petrologic processes. As a starting point for apatite-system thermodynamics, Hovis and Harlov (2010, American Mineralogist 95, 946-952) reported enthalpies of mixing for a F-Cl apatite series. Harlov synthesized all such crystalline solutions at the GFZ-Potsdam using a slow-cooled molten-flux method. In order to expand thermodynamic characterization of the F-Cl-OH apatite system, a new study has been initiated along the F-OH apatite binary. Synthesis of this new series made use of National Institute of Standards and Technology (NIST) 2910a hydroxylapatite, a standard reference material made at NIST "by solution reaction of calcium hydroxide with phosphoric acid." Synthesis efforts at Lafayette College have been successful in producing fluorapatite through ion exchange between hydroxylapatite 2910a and fluorite. In these experiments, a thin layer of hydroxylapatite powder was placed on a polished CaF2 disc (obtained from a supplier of high-purity crystals for spectroscopy), pressed firmly against the disc, then annealed at 750 °C (1 bar) for three days. Longer annealing times did not produce further change in unit-cell dimensions of the resulting fluorapatite, but it is uncertain at this time whether this procedure produces a pure-F end member (chemical analyses to be performed in the near future). It is clear from the unit-cell dimensions, however, that the newly synthesized apatite contains a high percentage of fluorine, probably greater than 90 mol % F. Intermediate compositions for a F-OH apatite series were made by combining 2910a hydroxylapatite powder with the newly synthesized fluorapatite in various proportions, then conducting chemical homogenization experiments at 750 °C on each mixture. X-ray powder diffraction data indicated that these experiments were successful in producing chemically homogeneous

  2. The biomimetic apatite-cefalotin coatings on modified titanium.

    PubMed

    Kang, Min-Kyung; Lee, Sang-Bae; Moon, Seung-Kyun; Kim, Kwang-Mahn; Kim, Kyoung-Nam

    2012-02-01

    Dental implant failure often occurs due to oral bacterial infection. The aim of this study was to demonstrate that antibiotic efficacy could be enhanced with modified titanium. First, the titanium was modified by anodization and heat-treatment. Then, a biomimetic coating process was completed in two steps. Surface characterization was performed with scanning electron microscopy, energy dispersive spectroscopy, and X-ray diffraction. Release of antibiotic was evaluated by UV/VIS spectrometry, and the antibacterial effect was evaluated on Streptococcus mutans. After the second coating step, we observed a thick homogeneous apatite layer that contained the antibiotic, cefalotin. The titanium formed a rutile phase after the heat treatment, and a carbonated apatite phase appeared after biomimetic coating. We found that the modified titanium increased the loading of cefalotin onto the hydroxyapatite coated surface. The results suggested that modified titanium coated with a cefalotin using biomimetic coating method might be useful for preventing local post-surgical implant infections. PMID:22277612

  3. Laser-SNMS analysis of apatite formation in vitro

    NASA Astrophysics Data System (ADS)

    Dambach, S.; Fartmann, M.; Kriegeskotte, C.; Brüning, C.; Wiesmann, H. P.; Lipinsky, D.; Arlinghaus, H. F.

    2004-06-01

    We have applied nonresonant laser secondary neutral mass spectrometry (Laser-SNMS) to examine different states of biomineralization in vitro. Primary osteoblast-like cells derived from bovine metacarpals were cultured for 5 weeks on clean smooth silicon substrates. For mass spectrometric investigations, the cells and newly formed mineral were cryofixed, freeze-fractured, and freeze-dried. The results indicate that in the vicinity of single osteoblasts, extracellular enrichment of potassium typically occurs during the initial stages of mineralization. Potassium may interact with matrix macromolecules and prevent an uncontrolled apatite deposition. However, apatite biomineral formation is correlated with a potassium release. In conclusion, potassium seems to be involved in the process of extracellular matrix biomineralization.

  4. Situ formation of apatite for sequestering radionuclides and heavy metals

    DOEpatents

    Moore, Robert C.

    2003-07-15

    Methods for in situ formation in soil of a permeable reactive barrier or zone comprising a phosphate precipitate, such as apatite or hydroxyapatite, which is capable of selectively trapping and removing radionuclides and heavy metal contaminants from the soil, while allowing water or other compounds to pass through. A preparation of a phosphate reagent and a chelated calcium reagent is mixed aboveground and injected into the soil. Subsequently, the chelated calcium reagent biodegrades and slowly releases free calcium. The free calcium reacts with the phosphate reagent to form a phosphate precipitate. Under the proper chemical conditions, apatite or hydroxyapatite can form. Radionuclide and heavy metal contaminants, including lead, strontium, lanthanides, and uranium are then selectively sequestered by sorbing them onto the phosphate precipitate. A reducing agent can be added for reduction and selective sequestration of technetium or selenium contaminants.

  5. Synthesis and characterization of strontium-lanthanum apatites

    SciTech Connect

    Boughzala, K.; Salem, E. Ben; Chrifa, A. Ben; Gaudin, E.; Bouzouita, K. . E-mail: khaled.bouzouita@ipeim.rnu.tn

    2007-07-03

    Two series of strontium-lanthanum apatites, Sr{sub 10-x}La {sub x}(PO{sub 4}){sub 6-x}(SiO{sub 4}) {sub x}F{sub 2} and Sr{sub 10-x}La {sub x}(PO{sub 4}){sub 6-x}(SiO{sub 4}) {sub x}O with 0 {<=} x {<=} 6, were synthesized by solid state reaction in the temperature range of 1200-1400 deg. C. The obtained materials were characterized by powder X-ray diffraction, infrared absorption spectroscopy and solid {sup 31}P Nuclear Magnetic Resonance. Pure solid solutions were obtained within a limited range of unsubstituted phosphate and silicate apatites. A variation of the lattice parameters was observed, with an increase of a and a decrease of c parameters, related to the radius of the corresponding substituted ions.

  6. Apatite fission-track thermochronology of the Pennsylvania Appalachian Basin

    NASA Astrophysics Data System (ADS)

    Roden, Mary K.; Miller, Donald S.

    1989-09-01

    Thirty-four apatite fission-track apparent ages and twenty-four track length distributions for ash bed samples from the Valley and Ridge Province and Upper Devonian to Upper Pennsylvania sedimentary samples from the Allegheny Front and Allegheny Plateau of Pennsylvania suggest that these regions represent different thermal (uplift) regimes as well as different structural provinces. The Valley and Ridge Province Tioga and Kalkberg ash bed samples yield apatite fission-track apparent ages and track length distributions that indicate early post-Alleghanian (285-270 Ma) cooling and unroofing that began at ˜250 Ma. Assuming a geothermal gradient of 25°C km -1, a burial depth of at least 3.4 km can be estimated for all the Pennsylvania samples. At the Allegheny structural front and on the western Allegheny Plateau, the apatite fission-track apparent ages (<150 Ma) and track length measurements indicate a Late Jurassic-Early Cretaceous thermal event for these samples possibly resulting from a higher geothermal gradient coinciding with kimberlite intrusion at this time along the Greene-Potter Fault Zone. In northeast Pennsylvania on the Allegheny Plateau, the Upper Paleozoic sedimentary samples yield apatite fission-track apparent ages ≤180 Ma. Narrow track length distributions with long mean lengths (13-14 μm) and small standard deviations (1.3 μm) suggest rapid cooling from temperatures >110°C during the Middle Jurassic-Early Cretaceous for this part of Pennsylvania. This is consistent with the suggested uplift history of the Catskill Mountain region in adjacent New York State.

  7. Materials testing for in situ stabilization treatability study of INEEL mixed wastes soils

    SciTech Connect

    Heiser, J.; Fuhrmann, M.

    1997-09-01

    This report describes the contaminant-specific materials testing phase of the In Situ Stabilization Comprehensive Environment Response, Compensation, and Liability Act (CERCLA) Treatability Study (TS). The purpose of materials testing is to measure the effectiveness of grouting agents to stabilize Idaho National Engineering and Environmental Laboratory (INEEL) Acid Pit soils and select a grout material for use in the Cold Test Demonstration and Acid Pit Stabilization Treatability Study within the Subsurface Disposal Area (SDA) at the Radioactive Waste Management Complex (RWMC). Test results will assist the selecting a grout material for the follow-on demonstrations described in Test Plan for the Cold Test Demonstration and Acid Pit Stabilization Phases of the In Situ Stabilization Treatability Study at the Radioactive Waste Management Complex.

  8. Characterization of apatite formed on alkaline-heat-treated Ti.

    PubMed

    Chosa, N; Taira, M; Saitoh, S; Sato, N; Araki, Y

    2004-06-01

    Alkaline-heat-treated titanium self-forms an apatite surface layer in vivo. The aim of the present study was to materialistically characterize the surface of alkaline-heat-treated titanium immersed in simulated body fluid (AHS-TI) and to examine the differentiation behavior of osteoblasts on AHS-TI. SEM, thin-film XRD, FTIR, and XPS analyses revealed that AHS-TI contained a 1.0- micro m-thick, low-crystalline, and [002] direction-oriented carbonate apatite surface. Human osteoblast-like SaOS-2 cells were cultured on polystyrene, titanium, and AHS-TI, and RT-PCR analyses of osteogenic differentiation-related mRNAs were conducted. On AHS-TI, the expression of bone sialoprotein mRNA was up-regulated as compared with that on polystyrene and titanium (p < 0.05). On AHS-TI, the expression of osteopontin and osteocalcin mRNAs was up-regulated as compared with that on polystyrene (p<0.05). The results indicate that the apatite was bone-like and accelerated the osteogenic differentiation of SaOS-2, suggesting that alkaline-heat treatment might facilitate better integration of titanium implants with bone. PMID:15153453

  9. Citrate occurs widely in healthy and pathological apatitic biomineral: mineralized articular cartilage, and intimal atherosclerotic plaque and apatitic kidney stones.

    PubMed

    Reid, David G; Duer, Melinda J; Jackson, Graham E; Murray, Rachel C; Rodgers, Allen L; Shanahan, Catherine M

    2013-09-01

    There is continuing debate about whether abundant citrate plays an active role in biomineralization of bone. Using solid state NMR dipolar dephasing, we examined another normally mineralized hard tissue, mineralized articular cartilage, as well as biocalcifications arising in pathological conditions, mineralized intimal atherosclerotic vascular plaque, and apatitic uroliths (urinary stones). Residual nondephasing ¹³C NMR signal at 76 ppm in the spectra of mineralized cartilage and vascular plaque indicates that a quaternary carbon atom resonates at this frequency, consistent with the presence of citrate. The presence, and as yet unproven possible mechanistic involvement, of citrate in tissue mineralization extends the compositional, structural, biogenetic, and cytological similarities between these tissues and bone itself. Out of 10 apatitic kidney stones, five contained NMR-detectable citrate. Finding citrate in a high proportion of uroliths may be significant in view of the use of citrate in urolithiasis therapy and prophylaxis. Citrate may be essential for normal biomineralization (e.g., of cartilage), play a modulatory role in vascular calcification which could be a target for therapeutic intervention, and drive the formation of apatitic rather than other calcific uroliths, including more therapeutically intractable forms of calcium phosphate. PMID:23780351

  10. Partition coefficients of Hf, Zr, and REE between zircon, apatite, and liquid

    USGS Publications Warehouse

    Fujimaki, H.

    1986-01-01

    Concentration ratios of Hf, Zr, and REE between zircon, apatite, and liquid were determined for three igneous compositions: two andesites and a diorite. The concentration ratios of these elements between zircon and corresponding liquid can approximate the partition coefficient. Although the concentration ratios between apatite and andesite groundmass can be considered as partition coefficients, those for the apatite in the diorite may deviate from the partition coefficients. The HREE partition coefficients between zircon and liquid are very large (100 for Er to 500 for Lu), and the Hf partition coefficient is even larger. The REE partition coefficients between apatite and liquid are convex upward, and large (D=10-100), whereas the Hf and Zr partition coefficients are less than 1. The large differences between partition coefficients of Lu and Hf for zircon-liquid and for apatite-liquid are confirmed. These partition coefficients are useful for petrogenetic models involving zircon and apatite. ?? 1986 Springer-Verlag.

  11. Potential routes to carbon inclusion in apatite minerals: a DFT study

    NASA Astrophysics Data System (ADS)

    Rabone, J. A. L.; de Leeuw, N. H.

    2007-09-01

    We have conducted a computational study to investigate a number of possible routes for the incorporation of carbon into apatites. Using density functional theory (DFT) we have calculated geometry optimised structures for fluor- and hydroxy-apatites with and without various substitutions. We have studied several different carbonate substitutions, pure carbonate and pure formate apatites, neutral carbon atoms occupying interstices, and carbon dioxide and acetylene absorbed in oxyapatite.

  12. [Age and gender changes of apatites from human hard tooth tissues].

    PubMed

    Pikhur, O L; Ryzhak, G A; Iordanishvili, A K; Iankovskiĭ, V V; D'iakonov, M M

    2014-01-01

    Apatites of hard tissues of teeth of persons of different sex and age were studied in detail. It is shown that the crystal structure of apatites depends on changes in the composition of the enamel that happen during a person's life. Limits of the variations of the crystal lattice parameters of the enamel apatites connected with the complicate processes of de- and remineralization have been determined. On the basis of the identified correlations between chemical composition, crystal lattice parameters and age of patients, the complicated interrelated isomorphic replacements occurring in the crystal structure of apatites of hard tooth tissues during aging were analysed. PMID:25946859

  13. Lu-Hf and PbSL geochronology of apatites from Proterozoic terranes: A first look at Lu-Hf isotopic closure in metamorphic apatite

    NASA Astrophysics Data System (ADS)

    Barfod, Gry Hoffmann; Krogstad, Eirik Jens; Frei, Robert; Albarède, Francis

    2005-04-01

    The mineral apatite is characterized by elevated and highly variable Lu/Hf ratios that, in some cases, allow for single-crystal dating by the Lu-Hf isotopic system. Apatites from the Adirondack Lowlands and Otter Lake area in the Grenville Province, and from the Black Hills, South Dakota, yield Lu-Hf ages that are consistently older than their respective Pb step leaching ages. Isotopic closure for the Lu-Hf system, therefore, occurs before U-Pb system closure in this mineral. In the Adirondack Lowlands, where H 2O activity was low, Lu-Hf systematics of cm-sized apatite crystals remained undisturbed during upper amphibolite facies metamorphism (˜700 to 675 °C) at 1170-1130 Ma. The relatively old Lu-Hf ages of 1270 and 1230 Ma observed for these apatites correlate with decreasing crystal size. In contrast, apatite from the fluid-rich Otter Lake area and Black Hills yields unrealistically low apparent Lu-Hf closure temperatures, implying that in these apatites, fluids facilitated late exchange. The Lu-Hf ages for the metamorphic apatites were thus controlled either by the prevailing temperature and grain size, or by fluid activity.

  14. BIOLOGICAL TREATABILITY OF KRW ENERGY SYSTEMS GASIFIER PDU (PROCESS DEVELOPMENT UNIT) WASTEWATERS

    EPA Science Inventory

    The report gives results of bench-scale biological treatability tests with wastewaters produced from the KRW Energy Systems gasifier process development unit (KRW-PDU). Goals of the tests were to assess the biotreatability of these aqueous wastes and to develop data for correlati...

  15. Innovative Approach for Development of Drinking Water Research Data in the EPA Treatability Database

    EPA Science Inventory

    In recent years, funding for development of the TDB has been limited due to Federal budget constraints. As a result, EPA adopted an innovative approach to continue the development of new contaminants and maintenance of treatability information on over 60 existing drinking water ...

  16. SUPERFUND TREATABILITY CLEARINGHOUSE: TRIAL BURN TEST REPORT, PART 1 - DATA SUMMARIES

    EPA Science Inventory

    This treatability study summary reports on the results of a trial burn of pesticide-contaminated soil from the Aberdeen, NC Superfund site. The trial burn using the Vesta mobile rotary kiln incinerator was designed to demonstrate that this system can destroy the pestici...

  17. GUIDE FOR CONDUCTING TREATABILITY STUDIES UNDER CERCLA: SOLVENT EXTRACTION - INTERIM GUIDANCE

    EPA Science Inventory

    Systematically conducted, well-documented treatability studies are an important component of the remedial investigation/feasibility study (RI/FS) process and the remedial design/remedial action (RD/RA) process under the Comprehensive Environmental Response, Compensation and Liabi...

  18. GUIDE TO CONDUCTING TREATABILITY STUDIES UNDER CERCLA: SOIL WASHING - INTERIM GUIDANCE

    EPA Science Inventory

    Systematically conducted, well-documented treatability studies are an important component of the remedial investigation/feasibility study (RI/FS) process and the remedial design/remedial action (RD/RA) process under the Comprehensive Environmental Response, Compensation, and Liab...

  19. SUPERFUND TREATABILITY CLEARINGHOUSE: CERCLA BDAT SARM PREPARATION AND RESULTS OF PHYSICAL SOILS WASHING EXPERIMENTS (FINAL REPORT)

    EPA Science Inventory

    This study reports on the results of work preparing 30,000 Ibs of SARM or synthetic analytical reference matrix, a surrogate Superfund soil containing a vide range of contaminants. It also reports the results ©f bench scale treatability experiments designed to simulate the EP...

  20. In-Situ Chemical Reduction and Oxidation of VOCs in Groundwater: Groundwater Treatability Studies

    NASA Technical Reports Server (NTRS)

    Keith, Amy; Glasgow, Jason; McCaleh, Rececca C. (Technical Monitor)

    2001-01-01

    This paper presents NASA Marshall Space Flight Center's treatability studies for volatile organic compounds in groundwater. In-Situ groundwater treatment technologies include: 1) Chemical Reduction(Ferox); 2) Chemical Oxidation (Fenton Reagents, Permanganate, and Persulfate); and 3) Thermal (Dynamic Underground Stripping, Six-Phase Heating). This paper is presented in viewgraph form.

  1. SUPERFUND TREATABILITY CLEARINGHOUSE: INPUT/OUTPUT DATA FOR SEVERAL TREATMENT TECHNOLOGIES

    EPA Science Inventory

    This treatability study is a pilot-scale evaluation of a thin-film evaporator (TFE) for volatile organics (VO) removal from oily sludges such as refinery sludges. TFEs were studied to evaluate their use to remove and recover VO from these sludges prior to land treatment. This w...

  2. SUPERFUND TREATABILITY CLEARINGHOUSE: EXTRACTIVE METHODS FOR SOIL DECONTAMINATION, A GENERAL SURVEY AND REVIEW OPERATIONAL TREATMENT INSTALLATIONS

    EPA Science Inventory

    The treatability study report provides a general overview of soil decontamination by extraction and reports on the field application of three specific different soil washing/solvent extraction systems. Each system is similar in design and removed contaminants from soil includ...

  3. Innovative Approach for Development of Drinking Water Research Data in the EPA Treatability Database - abstract

    EPA Science Inventory

    In recent years, funding for development of the TDB has been limited due to Federal budget constraints. As a result, EPA adopted an innovative approach to continue the development of new contaminants and maintenance of treatability information on over 60 existing drinking water ...

  4. Crystal Chemistry of Th in Apatite: Geochemistry and Environmental Implications

    NASA Astrophysics Data System (ADS)

    Luo, Y.; Rakovan, J.; Elzinga, E.; Pan, Y.; Hughes, J.

    2006-05-01

    Understanding the crystal chemistry of nuclear waste forms is critical to proper evaluation of their potential use and stability. Because of apatite's ability to incorporate rare earth elements and actinides, there is great interest in it as a solid nuclear waste form and an engineered contaminant barrier. However, the crystal chemistry of actinides in the apatite structure is still poorly understood. Through the complementary use of single crystal X-ray diffraction and X-ray absorption spectroscopy, we present here the first direct results on the site occupancy of thorium in apatite structure and the structural distortion created by its substitution. Single crystal X-ray diffraction data were used to refine the structure and site occupancies of a synthetic fluorapatite with approximately 2 wt% Th in the structure. The structure refinements of three separate crystals with R = 0.0167-0.0217 indicate that Th substitutes almost extensively into the Ca2 site. The value of ThCa(2)/ThCa(1), calculated per individual site to account for the different multiplicity of the two Ca sites, is 6.5. X-ray absorption spectroscopy was used to probe the local structure of Th in this synthetic fluorapatite (single crystal form), as well as Th in a natural fluorapatite (powder form) from Mineville, NY with the Th concentration of approximately 2000 ppm. The results from extend X-ray absorption fine structure (EXAFS) also indicate that Th partitions into the Ca2 site and yields Th specific bond distances which are not obtainable from single crystal X-ray diffraction.

  5. Thermal expansion of solid solutions in apatite binary systems

    SciTech Connect

    Knyazev, Alexander V.; Bulanov, Evgeny N. Korokin, Vitaly Zh.

    2015-01-15

    Graphical abstract: Thermal dependencies of volume thermal expansion parameter for with thermal expansion diagrams for Pb{sub 5}(PO{sub 4}){sub 3}F{sub x}Cl{sub 1−x}. - Highlights: • Solid solutions in three apatitic binary systems were investigated via HT-XRD. • Thermal expansion coefficients of solid solutions in the systems were calculated. • Features of the thermal deformation of the apatites were described. • Termoroentgenography is a sensitive method for the investigation of isomorphism. - Abstract: High-temperature insitu X-ray diffraction was used to investigate isomorphism and the thermal expansion of apatite-structured compounds in three binary systems in the entire temperature range of the existence of its hexagonal modifications. Most of the studied compounds are highly expandable (α{sub l} > 8 × 10{sup 6} (K{sup −1})). In Pb{sub 5}(PO{sub 4}){sub 3}F–Pb{sub 5}(PO{sub 4}){sub 3}Cl system, volume thermal expansion coefficient is independence from the composition at 573 K. In Pb{sub 5}(PO{sub 4}){sub 3}Cl–Pb{sub 5}(VO{sub 4}){sub 3}Cl, the compound with equimolar ratio of substituted atoms has constant volume thermal expansion coefficient in temperature range 298–973 K. Ca{sub 5}(PO{sub 4}){sub 3}Cl–Pb{sub 5}(PO{sub 4}){sub 3}Cl system is characterized by the most thermal sensitive composition, in which there is an equal ratio of isomorphic substituted atoms.

  6. Developing biogeochemical tracers of apatite weathering by ectomycorrhizal fungi

    NASA Astrophysics Data System (ADS)

    Vadeboncoeur, M. A.; Bryce, J. G.; Hobbie, E. A.; Meana-Prado, M. F.; Blichert-Toft, J.

    2012-12-01

    Chronic acid deposition has depleted calcium (Ca) from many New England forest soils, and intensive harvesting may reduce phosphorus (P) available to future rotations. Thin glacial till soils contain trace amounts of apatite, a primary calcium phosphate mineral, which may be an important long-term source of both P and Ca to ecosystems. The extent to which ECM fungi enhance the weathering rate of primary minerals in soil which contain growth-limiting nutrients remains poorly quantified, in part due to biogeochemical tracers which are subsequently masked by within-plant fractionation. Rare earth elements (REEs) and Pb isotope ratios show some potential for revealing differences in soil apatite weathering rates across forest stands and silvicultural treatments. To test the utility of these tracers, we grew birch seedlings semi-hydroponically under controlled P-limited conditions, supplemented with mesh bags containing granite chips. Our experimental design included nonmycorrhizal (NM) as well as ectomycorrhizal cultures (Cortinarius or Leccinum). Resulting mycorrhizal roots and leachates of granite chips were analyzed for these tracers. REE concentrations in roots were greatly elevated in treatments with granite relative to those without granite, demonstrating uptake of apatite weathering products. Roots with different mycorrhizal fungi accumulated similar concentrations of REEs and were generally elevated compared to the NM cultures. Ammonium chloride leaches of granite chips grown in contact with mycorrhizal hyphae show elevated REE concentrations and significantly radiogenic Pb isotope signatures relative to bulk rock, also supporting enhanced apatite dissolution. Our results in culture are consistent with data from field-collected sporocarps from hardwood stands in the Bartlett Experimental Forest in New Hampshire, in which Cortinarius sporocarp Pb isotope ratios were more radiogenic than those of other ectomycorrhizal sporocarps. Taken together, the experimental

  7. H-Isotopic Composition of Apatite in Northwest Africa 7034

    NASA Technical Reports Server (NTRS)

    McCubbin, F. M.; Barnes, J. J.; Santos, A. R.; Boyce, J. W.; Anand, M.; Franchi, I. A.; Agee, C. B.

    2016-01-01

    Northwest Africa (NWA) 7034 and its pairings comprise a regolith breccia with a basaltic bulk composition [1] that yields a better match than any other martian meteorite to estimates of Mars' bulk crust composition [1]. Given the similarities between NWA 7034 and the martian crust, NWA 7034 may represent an important sample for constraining the crustal composition of components that cannot be measured directly by remote sensing. In the present study, we seek to constrain the H isotopic composition of the martian crust using Cl-rich apatite in NWA 7034.

  8. Pilot-scale treatability test plan for the 200-UP-1 groundwater Operable Unit

    SciTech Connect

    Wittreich, C.D.

    1994-05-01

    This document presents the treatability test plan for pilot-scale pump and treat testing at the 200-UP-1 Operable Unit. This treatability test plan has been prepared in response to an agreement between the US Department of Energy, the US Environmental Protection Agency, and the Washington State Department of Ecology, as documented in Hanford Federal Facility Agreement and Consent Order (Ecology et al. 1989a) Change Control Form M-13-93-03 (Ecology et al. 1994). The agreement also requires that, following completion of the activities described in this test plan, a 200-UP-1 Operable Unit interim remedial measure (IRM) proposed plan be developed for use in preparing an interim action record of decision (ROD). The IRM Proposed Plan will be supported by the results of the testing described in this treatability test plan, as well as by other 200-UP-1 Operable Unit activities (e.g., limited field investigation, development of a qualitative risk assessment). Once issued, the interim action ROD will specify the interim action for groundwater contamination at the 200-UP-1 Operable Unit. The approach discussed in this treatability test plan is to conduct a pilot-scale pump and treat test for the contaminant plume associated with the 200-UP-1 Operable Unit. Primary contaminants of concern are uranium and technetium-99; the secondary contaminant of concern is nitrate. The pilot-scale treatability testing presented in this test plan has as its primary purpose to assess the performance of aboveground treatment systems with respect to the ability to remove the primary contaminants in groundwater withdrawn from the contaminant plume.

  9. Commercial treatability study capabilities for application to the US Department of Energy`s anticipated mixed waste streams. Revision 1

    SciTech Connect

    1996-09-01

    US DOE mixed low-level and mixed transuranic waste inventory was estimated at 181,000 cubic meters (about 2,000 waste streams). Treatability studies may be used as part of DOE`s mixed waste management program. Commercial treatability study suppliers have been identified that either have current capability in their own facilities or have access to licensed facilities. Numerous federal and state regulations, as well as DOE Order 5820.2A, impact the performance of treatability studies. Generators, transporters, and treatability study facilities are subject to regulation. From a mixed- waste standpoint, a key requirement is that the treatability study facility must have an NRC or state license that allows it to possess radioactive materials. From a RCRA perspective, the facility must support treatability study activities with the applicable plans, reports, and documentation. If PCBs are present in the waste, TSCA will also be an issue. CERCLA requirements may apply, and both DOE and NRC regulations will impact the transportation of DOE mixed waste to an off-site treatment facility. DOE waste managers will need to be cognizant of all applicable regulations as mixed-waste treatability study programs are initiated.

  10. In vitro apatite formation on polyamide containing carboxyl groups modified with silanol groups.

    PubMed

    Kawai, Takahiro; Ohtsuki, Chikara; Kamitakahara, Masanobu; Hosoya, Kayo; Tanihara, Masao; Miyazaki, Toshiki; Sakaguchi, Yoshimitsu; Konagaya, Shigeji

    2007-06-01

    Modification of organic polymer with silanol groups in combination with calcium salts enables the polymer to show bioactivity, that is, the polymer forms apatite on its surface after exposure to body environment. However, how modification with silanol groups influences ability of apatite formation on the polymer substrate and adhesive strength between polymer and apatite is not yet known. In the present study, polyamide containing carboxyl groups was modified with different amounts of silanol groups, and its apatite-forming ability in 1.5SBF, which contained ion concentrations 1.5 times those of simulated body fluid (SBF), was examined. The rate of apatite formation increased with increasing content of silanol groups in the polyamide films. This may be attributed to enhancement of dipole interactions. A tendency for the adhesive strength of the apatite layer on the polyamide film to be decreased with increasing content of silanol groups was observed. This may be attributed to swelling in 1.5SBF and having a high degree of shrinkage after drying. These findings clearly show that modification of organic polymers with the functional groups induces apatite deposition, and also determines the adhesive strength of the apatite layer to the organic substrates. PMID:17243002

  11. TREATMENT OF ACID MINE DRAINAGE USING FISHBONE APATITE IITM

    SciTech Connect

    Neal A. Yancey

    2006-10-01

    ABSTRACT. In 2000, a reactive barrier was installed on the East Fork of Ninemile Creek near Wallace, Idaho to treat acid mine discharge. The barrier was filled with fishbone derived Apatite IITM to remove the contaminants of concern (Zn, Pb, and Cd) and raise the pH of the acidic mine discharge. Metal removal has been achieved by a combination of chemical, biological, and physical precipitation. Flow for the water ranges from 5 to 35 gallons per minute. The water is successfully being treated, but the system experienced varying degrees of plugging. In 2002, gravel was mixed with the Apatite IITM to help control plugging. In 2003 the Idaho National Laboratory was ask to provide technical support to the Coeur d’Alene Basin Commission to help identify a remedy to the plugging issue. Air sparging was employed to treat the plugging issues. Plastic packing rings were added in the fall of 2005, which have increased the void space in the media and increased flows during the 10 months of operation since the improvements were made.

  12. Crystal growth of apatite by replacement of an aragonite precursor

    NASA Astrophysics Data System (ADS)

    Kasioptas, Argyrios; Geisler, Thorsten; Putnis, Christine V.; Perdikouri, Christina; Putnis, Andrew

    2010-08-01

    The replacement of aragonite by apatite is a process that occurs naturally during diagenesis, chemical weathering and natural hydrothermal reactions and is artificially promoted in medical sciences for use of the product material as a bone implant. We have investigated the mechanism and the kinetics of this replacement by using biogenic aragonite (cuttlebone of the Sepia officinalis) as a starting material and reacting it with di-ammonium hydrogen phosphate solution. Isothermal experiments were carried out over a range of temperatures up to 190 °C. Quantification of each solid phase, for different reaction times, was obtained by the Rietveld analysis of powder X-ray diffraction patterns. An empirical activation energy was calculated by using two different approaches to analyze the data. Scanning electron microscopy showed that the fine structure of the cuttlebone was perfectly retained even after aragonite had been completely converted to apatite. We present a detailed investigation of the kinetics of a reaction that involves interaction of a solid phase with an aqueous fluid and leads to a pseudomorphic replacement of the initial solid phase by a new, chemically different, phase. This replacement process is described in terms of an interface-coupled dissolution-reprecipitation mechanism.

  13. Self Attenuation of Gamma Rays in Titanite, Zircon and Apatite

    NASA Astrophysics Data System (ADS)

    Walsh, C. N.; Baskaran, M.; Brownlee, S. J.; Eakin, M.

    2013-12-01

    Several of the gamma-emitting U-Th series, cosmogenic and anthropogenic radionuclides (210Pb, 234Th, 226Ra, 228Ra, 7Be, 137Cs, etc) have been widely utilized as tracers and chronometers in environmental studies. Precise measurements of these nuclides using gamma-ray spectrometry in environmental matrices require that the proper correction factors for self- and external-absorption be applied. In this study, we examine factors associated with absorption and self attenuation of gamma-rays of 210Pb (46.5 keV), 234Th (63 keV), 226Ra (via 214Pb and 214Bi, 351.9 and 609 keV) and 228Ra (via 228Ac, 338.3 and 911.2 keV) using a well-type germanium gamma-ray detector. Samples of three naturally occurring minerals (titanite, apatite and zircon) were separated into 5 size fractions (<63 μm, 63-125 μm, 125-250 μm, 250-500 μm, and >500 μm) and analyzed for 210Pb, 234Th, 226Ra, and 228Ra. We also analyzed two synthetic silica standards (RGU-1, RGTH-1) that have a relatively uniform grain size of 63 μm. These minerals were chosen based on their varying chemical compositions and densities. Chosen samples are of an age that isotopes of 238U and 232Th are expected to be in secular equilibrium with their daughter products. However, the measured activity ratios between members of the family vary widely. In the case of titanite, the 210Pb/226Ra ratios in 5 size fractions varied between 0.44×0.03 and 0.53×0.03, while in apatite it varied between 0.54×0.03 and 0.67×0.04, without applying any self- and external-absorption correction factors. Using the attenuation coefficients of constituent elements at different energies, we estimate the attenuation coefficient for each of these 4 minerals and determine the self- and external-absorption correction factors. The self- and external-absorption corrected activities agree with the expected activities in these minerals. Our data suggests that variations in the activity levels are dependent on chemical composition, density, and grain

  14. Apatite precipitation on a novel fast-setting calcium silicate cement containing fluoride

    PubMed Central

    Ranjkesh, Bahram; Chevallier, Jacques; Salehi, Hamideh; Cuisinier, Frédéric; Isidor, Flemming; Løvschall, Henrik

    2016-01-01

    Abstract Aim: Calcium silicate cements are widely used in endodontics. Novel fast-setting calcium silicate cement with fluoride (Protooth) has been developed for potential applications in teeth crowns including cavity lining and cementation. Objective: To evaluate the surface apatite-forming ability of Protooth compositions as a function of fluoride content and immersion time in phosphate-buffered saline (PBS). Material and methods: Three cement compositions were tested: Protooth (3.5% fluoride and 10% radiocontrast), ultrafast Protooth (3.5% fluoride and 20% radiocontrast), and high fluoride Protooth (15% fluoride and 25% radiocontrast). Powders were cap-mixed with liquid, filled to the molds and immersed in PBS. Scanning electron microscopy, energy dispersive X-ray analysis, and Raman spectroscopy were used to characterize the precipitations morphology and composition after 1, 7, 28, and 56 days. Apatite/belite Raman peak height indicated the apatite thickness. Results: Spherical calcium phosphate precipitations with acicular crystallites were formed after 1-day immersion in PBS and Raman spectra disclosed the phosphate band at 965 cm−1, supporting the apatite formation over Protooth compositions. The apatite deposition continued and more voluminous precipitations were observed after 56 days over the surface of all cements. Raman bands suggested the formation of β-type carbonated apatite over Protooth compositions. High fluoride Protooth showed the most compact deposition with significantly higher apatite/belite ratio compared to Protooth and ultrafast Protooth after 28 and 56 days. Conclusions: Calcium phosphate precipitations (apatite) were formed over Protooth compositions after immersion in PBS with increasing apatite formation as a function of time. High fluoride Protooth exhibited thicker apatite deposition. PMID:27335901

  15. Incorporation of iodine into apatite structure: a crystal chemistry approach using Artificial Neural Network

    NASA Astrophysics Data System (ADS)

    Wang, Jianwei

    2015-06-01

    Materials with apatite crystal structure provide a great potential for incorporating the long-lived radioactive iodine isotope (129I) in the form of iodide (I-) from nuclear waste streams. Because of its durability and potentially high iodine content, the apatite waste form can reduce iodine release rate and minimize the waste volume. Crystal structure and composition of apatite was investigated for iodide incorporation into the channel of the structure using Artificial Neural Network. A total of 86 experimentally determined apatite crystal structures of different compositions were compiled from literature, and 46 of them were used to train the networks and 42 were used to test the performance of the trained networks. The results show that the performances of the networks are satisfactory for predictions of unit cell parameters a and c and channel size of the structure. The trained and tested networks were then used to predict unknown compositions of apatite that incorporates iodide. With a crystal chemistry consideration, chemical compositions that lead to matching the size of the structural channel to the size of iodide were then predicted to be able to incorporate iodide in the structural channel. The calculations suggest that combinations of A site cations of Ag+, K+, Sr2+, Pb2+, Ba2+, and Cs+, and X site cations, mostly formed tetrahedron, of Mn5+, As5+, Cr5+, V5+, Mo5+, Si4+, Ge4+, and Re7+ are possible apatite compositions that are able to incorporate iodide. The charge balance of different apatite compositions can be achieved by multiple substitutions at a single site or coupled substitutions at both A and X sites. The results give important clues for designing experiments to synthesize new apatite compositions and also provide a fundamental understanding how iodide is incorporated in the apatite structure. This understanding can provide important insights for apatite waste forms design by optimizing the chemical composition and synthesis procedure.

  16. Endogenous Lunar Volatiles: Insights into the Abundances of Volatiles in the Moon from Lunar Apatite

    NASA Technical Reports Server (NTRS)

    McCubbin, Francis

    2016-01-01

    At the time of publication of New Views of the Moon, it was thought that the Moon was bone dry with less than about 1 ppb H2O. However in 2007, initial reports at the 38th Lunar and Planetary Science Conference speculated that H-species were present in both apatites and pyroclastic volcanic lunar glasses. These early reports were later confirmed through peer-review, which motivated many subsequent studies on magmatic volatiles in and on the Moon within the last decade. Some of these studies have cast into question the post-Apollo view of lunar formation, the distribution and sources of volatiles in the Earth-Moon system, and the thermal and magmatic evolution of the Moon. The mineral apatite has been one of the pillars of this new field of study, and it will be the primary focus of this abstract. Although apatite has been used both to understand the abundances of volatiles in lunar systems as well as the isotopic compositions of those volatiles, the focus here will be on the abundances of F, Cl, and H2O. This work demonstrates the utility of apatite in advancing our understanding of lunar volatiles, hence apatite should be among the topics covered in the endogenous lunar volatile chapter in NVM II. Truncated ternary plot of apatite X-site occupancy (mol%) from highlands apatite and mare basalt apatite plotted on the relative volatile abundance diagram from. The solid black lines delineate fields of relative abundances of F, Cl, and H2O (on a weight basis) in the melt from which the apatite crystallized. The diagram was constructed using available apatite/melt partitioning data for fluorine, chlorine, and hydroxyl.

  17. Pilot-scale treatability test plan for the 200-BP-5 operable unit

    SciTech Connect

    Not Available

    1994-08-01

    This document presents the treatability test plan for pilot-scale pump and treat testing at the 200-BP-5 Operable Unit. This treatability test plan has been prepared in response to an agreement between the U.S. Department of Energy (DOE), the U.S. Environmental Protection Agency (EPA), and the State of Washington Department of Ecology (Ecology), as documented in Hanford Federal Facility Agreement and Consent Order (Tri-Party Agreement, Ecology et al. 1989a) Change Control Form M-13-93-03 (Ecology et al. 1994) and a recent 200 NPL Agreement Change Control Form (Appendix A). The agreement also requires that, following completion of the activities described in this test plan, a 200-BP-5 Operable Unit Interim Remedial Measure (IRM) Proposed Plan be developed for use in preparing an Interim Action Record of Decision (ROD). The IRM Proposed Plan will be supported by the results of this treatability test plan, as well as by other 200-BP-5 Operable Unit activities (e.g., development of a qualitative risk assessment). Once issued, the Interim Action ROD will specify the interim action(s) for groundwater contamination at the 200-BP-5 Operable Unit. The treatability test approach is to conduct a pilot-scale pump and treat test for each of the two contaminant plumes associated with the 200-BP-5 Operable Unit. Primary contaminants of concern are {sup 99}Tc and {sup 60}Co for underwater affected by past discharges to the 216-BY Cribs, and {sup 90}Sr, {sup 239/240}Pu, and Cs for groundwater affected by past discharges to the 216-B-5 Reverse Well. The purpose of the pilot-scale treatability testing presented in this testplan is to provide the data basis for preparing an IRM Proposed Plan. To achieve this objective, treatability testing must: Assess the performance of groundwater pumping with respect to the ability to extract a significant amount of the primary contaminant mass present in the two contaminant plumes.

  18. Effects of the method of apatite seed crystals addition on setting reaction of α-tricalcium phosphate based apatite cement.

    PubMed

    Tsuru, Kanji; Ruslin; Maruta, Michito; Matsuya, Shigeki; Ishikawa, Kunio

    2015-10-01

    Appropriate setting time is an important parameter that determines the effectiveness of apatite cement (AC) for clinical application, given the issues of crystalline inflammatory response phenomena if AC fails to set. To this end, the present study analyzes the effects of the method of apatite seed crystals addition on the setting reaction of α-tricalcium phosphate (α-TCP) based AC. Two ACs, both consisting of α-TCP and calcium deficient hydroxyapatite (cdHAp), were analyzed in this study. In one AC, cdHAp was added externally to α-TCP and this AC was abbreviated as AC(EA). In the other AC, α-TCP was partially hydrolyzed to form cdHAp on the surface of α-TCP. This AC was referred to as AC(PH). Results indicate a decrease in the setting time of both ACs with the addition of cdHAp. Among them, for the given amount of added cdHAp, AC(PH) showed relatively shorter setting time than AC(EA). Besides, the mechanical strength of the set AC(PH) was also higher than that of set AC(EA). These properties of AC(PH) were attributed to the predominant crystal growth of cdHAp in the vicinity of the α-TCP particle surface. Accordingly, it can be concluded that the partial hydrolysis of α-TCP may be a better approach to add low crystalline cdHAp onto α-TCP based AC. PMID:26411440

  19. SUPERFUND TREATABILITY CLEARINGHOUSE: FINAL REPORT: DEVELOPMENT OF OPTIMUM TREATMENT SYSTEM FOR WASTEWATER LAGOONS PHASE II - SOLVENT EXTRACTION LABORATORY TESTING

    EPA Science Inventory

    The U.S. Army surveyed innovative treatment techniques for restoration of hazardous waste lagoons and selected solvent extraction as cost-effective restoration for further study. This treatability study focuses on treatment of organic (explosive) contaminated lagoon sediments w...

  20. Distribution of halogens between fluid and apatite during fluid-mediated replacement processes

    NASA Astrophysics Data System (ADS)

    Kusebauch, Christof; John, Timm; Whitehouse, Martin J.; Klemme, Stephan; Putnis, Andrew

    2015-12-01

    Apatite (Ca5(PO4)3(OH, F, Cl)) is one of the main host of halogens in magmatic and metamorphic rocks and plays a unique role during fluid-rock interaction as it incorporates halogens (i.e. F, Cl, Br, I) and OH from hydrothermal fluids to form a ternary solid solution of the endmembers F-apatite, Cl-apatite and OH-apatite. Here, we present an experimental study to investigate the processes during interaction of Cl-apatite with different aqueous solutions (KOH, NaCl, NaF of different concentration also doped with NaBr, NaI) at crustal conditions (400-700 °C and 0.2 GPa) leading to the formation of new apatite. We use the experimental results to calculate partition coefficients of halogens between apatite and fluid. Due to a coupled dissolution-reprecipitation mechanism new apatite is always formed as a pseudomorphic replacement of Cl-apatite. Additionally, some experiments produce new apatite also as an epitaxial overgrowth. The composition of new apatite is mainly governed by complex characteristics of the fluid phase from which it is precipitating and depends on composition of the fluid, temperature and fluid to mineral ratio. Furthermore, replaced apatite shows a compositional zonation, which is attributed to a compositional evolution of the coexisting fluid in local equilibrium with the newly formed apatite. Apatite/fluid partition coefficients for F depend on the concentration of F in the fluid and increase from 75 at high concentrations (460 μg/g F) to 300 at low concentrations (46 μg/g F) indicating a high compatibility of F in apatite. A correlation of Cl-concentration in apatite with Cl- concentration of fluid is not observed for experiments with highly saline solutions, composition of new apatite is rather governed by OH- concentration of the hydrothermal fluid. Low partition coefficients were measured for the larger halogens Br and I and vary between 0.7 * 10-3-152 * 10-3 for Br and 0.3 * 10-3-17 * 10-3 for I, respectively. Br seems to have D values of

  1. F-Cl-OH partitioning between biotite and apatite

    NASA Astrophysics Data System (ADS)

    Zhu, Chen; Sverjensky, Dimitri A.

    1992-09-01

    An assessment of F-C1-OH partitioning between natural apatite and biotite in a variety of rocks was used to evaluate reciprocal (Mg, Fe 2+, Al VI) (F, Cl, OH) mixing properties for biotite according to the reciprocal salt solution model of WOOD and NICHOLLS (1978). Ideal mixing of F-C1-OH and Fe-Mg-Al VI in the hydroxyl and octahedral sites is assumed for biotites with dilute Cl concentrations. The reciprocal interaction parameters, in terms of Gibbs free energies, for the reactions KMg3[ AlSi3O10]( OH) 2 + KFe3[ AlSi3O10]( F) 2 = KMg3[ AlSi3O10]( F) 2 + KFe3[ AlSi3O10]( OH) 2 Phl Fann Fphl Ann and KMg3[ AlSi3O10]( Cl) 2 + KFe3[ AlSi3O10]( OH) 2 = KMg3[ AlSi3O10]( OH) 2 + KFe3[ AlSi3O10] ( Cl) 2 Clphl Ann Phl Clann are about -10 kcal/mol and -4.5 kcal/mol, respectively. These mixing properties are consistent with standard state thermodynamic properties for F and Cl endmember phases from ZHU and SVERJENSKY (1991). The approach of studying F-C1-OH partitioning between biotite and apatite permits distinguishing the reciprocal effects from the effects of temperature, pressure, and fluid composition. The resultant mixing properties are consistent with observations both in hydrothermal experiments and in natural mineral assemblages. The mixing properties presented in this study enable us now to predict F and Cl concentrations of hydrothermal fluids from the measured F and Cl concentrations in biotite with variable Fe-Mg-Al VI proportions. A case study of the Santa Rita porphyry copper deposits, New Mexico, shows that hydrothermal fluids responsible for the phyllic alteration had a salinity about 3 molal Cl -, in agreement with fluid inclusion studies. Our internally consistent standard thermodynamic properties and solid solution models also lead to recalibration of the apatite-biotite geothermometer. The revised geothermometer predicts temperatures that agree with those estimated from other independent geothermometers. The large reciprocal effects in biotite also point

  2. Treatability studies on different refinery wastewater samples using high-throughput microbial electrolysis cells (MECs).

    PubMed

    Ren, Lijiao; Siegert, Michael; Ivanov, Ivan; Pisciotta, John M; Logan, Bruce E

    2013-05-01

    High-throughput microbial electrolysis cells (MECs) were used to perform treatability studies on many different refinery wastewater samples all having appreciably different characteristics, which resulted in large differences in current generation. A de-oiled refinery wastewater sample from one site (DOW1) produced the best results, with 2.1±0.2 A/m(2) (maximum current density), 79% chemical oxygen demand removal, and 82% headspace biological oxygen demand removal. These results were similar to those obtained using domestic wastewater. Two other de-oiled refinery wastewater samples also showed good performance, with a de-oiled oily sewer sample producing less current. A stabilization lagoon sample and a stripped sour wastewater sample failed to produce appreciable current. Electricity production, organics removal, and startup time were improved when the anode was first acclimated to domestic wastewater. These results show mini-MECs are an effective method for evaluating treatability of different wastewaters. PMID:23567698

  3. 300-FF-1 operable unit remedial investigation phase II report: Physical separation of soils treatability study

    SciTech Connect

    Not Available

    1994-04-01

    This report describes the approach and results of physical separations treatability tests conducted at the Hanford Site in the North Process Pond of the 300-FF-1 Operable Unit. Physical separation of soils was identified as a remediation alternative due to the potential to significantly reduce the amount of contaminated soils prior to disposal. Tests were conducted using a system developed at Hanford consisting of modified EPA equipment integrated with screens, hoppers, conveyors, tanks, and pumps from the Hanford Site. The treatability tests discussed in this report consisted of four parts, in which an estimated 84 tons of soil was processed: (1) a pre-test run to set up the system and adjust system parameters for soils to be processed; (2) a baseline run to establish the performance of the system - Test No. 1; (3) a final run in which the system was modified as a result of findings from the baseline run - Test No. 2; and (4) water treatment.

  4. Treatability studies for uranium and plutonium contaminated soils using physical separation methods. Environmental Assessment

    SciTech Connect

    1992-07-01

    The Nevada Field Office of the Department of Energy (DOE/NV) has stated in the Environmental Restoration and Waste Management (ERWM) Site Specific Plan for the Nevada Test Site (NTS) that DOE/NV is committed to achieving compliance with all applicable environmental laws, regulations, guidelines, and agreements covering operations at the NTS. The primary DOE/NV objective identified by the Site-Specific Plan is to comply with all laws and regulations aimed at protecting human health and the environment. These include Nevada statutes and regulations which may be applicable, including federally delegated authorities. This environmental assessment discusses limited bench-scale soil treatability testing of physical processes for decontamination of plutonium- and uranium-contaminated soil. The proposed location of these studies would be the Treatability Testing Facility (TTF), Building 3124 at Test Cell ``All in Area 25 of the NTS.

  5. Metallurgical Laboratory Treatability Study: An Analysis of Passive Soil Vapor Extraction Wells - June 2000 Update

    SciTech Connect

    Riha, B.D.

    2001-01-29

    The passive soil vapor extraction (PSVE) system at the MetLab of the Savannah River Site has been operating since May 1998. The results to date on the treatability study indicate the technology is performing well. Well concentrations are decreasing and contour maps of the vadose zone soil gas plume show a decrease in the extent of the plume. In the 2 years of operation approximately 270 pounds of chlorinated organic contaminants have been removed by natural barometric pumping of wells fitted with BaroBall valves (low pressure check valves). The PSVE system is performing well in a cost-effective manner. It is recommended that this system be allowed to continue operating to complete the remediation and to continue monitoring activities to verify and monitor the anticipated contaminant removal rates. The treatability study should be considered successfully completed and the remediation should be considered in full operation.

  6. Magnetic apatite for structural insights on the plasma membrane

    NASA Astrophysics Data System (ADS)

    Stanca, Sarmiza E.; Müller, Robert; Dellith, Jan; Nietzsche, Sandor; Stöckel, Stephan; Biskup, Christoph; Deckert, Volker; Krafft, Christoph; Popp, Jürgen; Fritzsche, Wolfgang

    2015-01-01

    The iron oxide-hydroxyapatite (FeOxHA) nanoparticles reported here differ from those reported before by their advantage of homogeneity and simple preparation; moreover, the presence of carboxymethyldextran (CMD), together with hydroxyapatite (HA), allows access to the cellular membrane, which makes our magnetic apatite unique. These nanoparticles combine magnetic behavior, Raman label ability and the property of interaction with the cellular membrane; they therefore represent an interesting material for structural differentiation of the cell membrane. It was observed by Raman spectroscopy, scanning electron microscopy (SEM) and fluorescence microscopy that FeOxHA adheres to the plasma membrane and does not penetrate the membrane. These insights make the nanoparticles a promising material for magnetic cell sorting, e.g. in microfluidic device applications.

  7. Calcium Solubility In Zeolite Synthetic-Apatite Mixtures

    NASA Technical Reports Server (NTRS)

    Beiersdorfer, R.; Ming, D. W.

    1999-01-01

    Life support systems at a lunar or martian outpost will require the ability to produce food growing in 1) treated lunar or martian regolith; 2) a synthetic soil, or 3) some combination of both. Zeoponic soil, composed of NH4 (-) and K-exchanged clinoptilolite (Cp) and synthetic apatite (Ap), can provide slow-release fertilization via dissolution and ion-exchange. Equilibrium studies indicate that KNH4, P, and Mg are available to plants at sufficient levels, however, Ca is deficient. Ca availability can be increased by adding a second Ca-bearing mineral: calcite (Cal); dolomite (Dol); or wollastonite (Wol). Additions of Cal, Dol, and Wol systematically change the concentrations of Ca and P in solution. Cal has the greatest effect, Dol the least, and Wol is intermediate.

  8. Apatite as probe for the halogen composition of metamorphic fluids (Bamble Sector, SE Norway)

    NASA Astrophysics Data System (ADS)

    Kusebauch, Christof; John, Timm; Whitehouse, Martin J.; Engvik, Ane K.

    2015-10-01

    Halogen composition of replaced apatite formed during a regional metasomatic event (Bamble Sector, SE Norway) reveals information about the composition and evolution of the hydrothermal fluid. Infiltration and pervasive fluid flow of highly saline fluids into gabbroic bodies lead to scapolitization and amphibolitization, where magmatic Cl-rich apatite reacts with the hydrothermal fluid to form OH- and/or F-rich apatite. Apatite from highly altered samples adjacent to the shear zone has highest F (up to 15,000 µg/g) and lowest Br (4-25 µg/g) concentrations, whereas apatite from least altered samples has very low F (30-200 µg/g) and high Br (30-85 µg/g). In addition, individual replaced apatite grains show a zonation in F with high concentrations along rims and cracks and low F in core regions. Iodine concentrations remain rather constant as low values of 0.18-0.70 µg/g. We interpret all observed compositional features of replaced apatite to be the result of a continuous evolution of the fluid during fluid-rock interaction. Due to its high compatibility, F from the infiltrating fluid is incorporated early into recrystallized apatite (close to shear zone and rims of individual apatite grains). In contrast, Br as an incompatible halogen becomes enriched in the fluid and is highest in the most evolved fluid. Using experimental partition data between replaced apatite and fluid, we calculated F concentrations of the evolving fluid to decrease from 60 to <1 µg/g and Br to increase from ~1200 to ~5000 µg/g; I concentrations of the fluid are constant in the order of 370 µg/g. Although Cl is expected to show a similar behavior as Br, replaced apatite has constant Cl concentrations throughout the alteration sequence (~1 wt.%), which is likely the result of a rather constant Cl activity in the fluid. Chlorine stable isotope values of individual apatite grains are heterogeneous and range from -1.2 to +3.7 ‰. High δ 37Cl values are generally correlated with OH

  9. Experimental Plan: Uranium Stabilization Through Polyphosphate Injection 300 Area Uranium Plume Treatability Demonstration Project

    SciTech Connect

    Wellman, Dawn M.; Fruchter, Jonathan S.; Vermeul, Vince R.

    2006-09-20

    This Test Plan describes a laboratory-testing program to be performed at Pacific Northwest National Laboratory (PNNL) in support of the 300-FF-5 Feasibility Study (FS). The objective of the proposed treatability test is to evaluate the efficacy of using polyphosphate injections to treat uranium contaminated groundwater in situ. This study will be used to: (1) Develop implementation cost estimates; (2) Identify implementation challenges; and (3) Investigate the technology's ability to meet remedial objectives These activities will be conducted in parallel with a limited field investigation, which is currently underway to more accurately define the vertical extent of uranium in the vadose zone, and in the capillary fringe zone laterally throughout the plume. The treatability test will establish the viability of the method and, along with characterization data from the limited field investigation, will provide the means for determining how best to implement the technology in the field. By conducting the treatability work in parallel with the ongoing Limited Field Investigation, the resulting Feasibility Study (FS) will provide proven, site-specific information for evaluating polyphosphate addition and selecting a suitable remediation strategy for the uranium plume within the FS time frame at an overall cost savings.

  10. Treatability studies for polyethylene encapsulation of INEL low-level mixed wastes. Final report

    SciTech Connect

    Lageraaen, P.R.; Patel, B.R.; Kalb, P.D.; Adams, J.W.

    1995-10-01

    Treatability studies for polyethylene encapsulation of Idaho National Engineering Laboratory (INEL) low-level mixed wastes were conducted at Brookhaven National Laboratory. The treatability work, which included thermal screening and/or processibility testing, was performed on priority candidate wastes identified by INEL to determine the applicability of polyethylene encapsulation for the solidification and stabilization of these mixed wastes. The candidate wastes selected for this preliminary study were Eutectic Salts, Ion Exchange Resins, Activated Carbons, Freon Contaminated Rags, TAN TURCO Decon 4502, ICPP Sodium Bearing Liquid Waste, and HTRE-3 Acid Spill Clean-up. Thermal screening was conducted for some of these wastes to determine the thermal stability of the wastes under expected pretreatment and processing conditions. Processibility testing to determine whether the wastes were amenable to extrusion processing included monitoring feed consistency, extruder output consistency, waste production homogeneity, and waste form performance. Processing parameters were not optimized within the scope of this study. However, based on the treatability results, polyethylene encapsulation does appear applicable as a primary or secondary treatment for most of these wastes.

  11. Operable Unit 7-13/14 in situ thermal desorption treatability study work plan

    SciTech Connect

    Shaw, P.; Nickelson, D.; Hyde, R.

    1999-05-01

    This Work Plan provides technical details for conducting a treatability study that will evaluate the application of in situ thermal desorption (ISTD) to landfill waste at the Subsurface Disposal Area (SDA) at the Idaho National Engineering and Environmental Laboratory (INEEL). ISTD is a form of thermally enhanced vapor vacuum extraction that heats contaminated soil and waste underground to raise its temperature and thereby vaporize and destroy most organics. An aboveground vapor vacuum collection and treatment system then destroys or absorbs the remaining organics and vents carbon dioxide and water to the atmosphere. The technology is a byproduct of an advanced oil-well thermal extraction program. The purpose of the ISTD treatability study is to fill performance-based data gaps relative to off-gas system performance, administrative feasibility, effects of the treatment on radioactive contaminants, worker safety during mobilization and demobilization, and effects of landfill type waste on the process (time to remediate, subsidence potential, underground fires, etc.). By performing this treatability study, uncertainties associated with ISTD as a selected remedy will be reduced, providing a better foundation of remedial recommendations and ultimate selection of remedial actions for the SDA.

  12. TREATABILITY TEST PLAN FOR DEEP VADOSE ZONE REMEDIATION AT THE HANFORD SITE CENTRAL PLATEAU

    SciTech Connect

    PETERSEN SW; MORSE JG; TRUEX MJ; LAST GV

    2007-11-29

    A treatability test plan has been prepared to address options for remediating portions of the deep vadose zone beneath a portion of the U.S. Department of Energy's (DOE's) Hanford Site. The vadose zone is the region of the subsurface that extends from the ground surface to the water table. The overriding objective of the treatability test plan is to recommend specific remediation technologies and laboratory and field tests to support the Comprehensive Environmental Response, Compensation, and Liability Act of 1980 and Resource Conservation and Recovery Act of 1976 remedial decision-making process in the Central Plateau of the Hanford Site. Most of the technologies considered involve removing water from the vadose zone or immobilizing the contaminants to reduce the risk of contaminating groundwater. A multi-element approach to initial treatability testing is recommended, with the goal of providing the information needed to evaluate candidate technologies. The proposed tests focus on mitigating two contaminants--uranium and technetium. Specific technologies are recommended for testing at areas that may affect groundwater in the future, but a strategy to test other technologies is also presented.

  13. Treatability Test Plan for Deep Vadose Zone Remediation at the Hanford Site's Central Plateau

    SciTech Connect

    Petersen, S.W.; Morse, J.G.; Truex, M.J.; Last, G.V.

    2008-07-01

    A treatability test plan has been prepared to address options for remediating portions of the deep vadose zone beneath the U.S. Department of Energy's (DOE's) Hanford Site. The vadose zone is the region of the subsurface that extends from the ground surface to the water table. The overriding objective of the treatability test plan is to recommend specific remediation technologies and laboratory and field tests to support the Comprehensive Environmental Response, Compensation, and Liability Act of 1980 and Resource Conservation and Recovery Act of 1976 remedial decision-making process in the Central Plateau of the Hanford Site. Most of the technologies considered involve removing water from the vadose zone or immobilizing the contaminants to reduce the risk of contaminating groundwater. A multi-element approach to initial treatability testing is recommended, with the goal of providing the information needed to evaluate candidate technologies. The proposed tests focus on mitigating two contaminants - uranium and technetium. Specific technologies are recommended for testing at areas that may affect groundwater in the future, but a strategy to test other technologies is also presented. (authors)

  14. Single-crystal apatite nanowires sheathed in graphitic shells: synthesis, characterization, and application.

    PubMed

    Jeong, Namjo; Cha, Misun; Park, Yun Chang; Lee, Kyung Mee; Lee, Jae Hyup; Park, Byong Chon; Lee, Junghoon

    2013-07-23

    Vertically aligned one-dimensional hybrid structures, which are composed of apatite and graphitic structures, can be beneficial for orthopedic applications. However, they are difficult to generate using the current method. Here, we report the first synthesis of a single-crystal apatite nanowire encapsulated in graphitic shells by a one-step chemical vapor deposition. Incipient nucleation of apatite and its subsequent transformation to an oriented crystal are directed by derived gaseous phosphorine. Longitudinal growth of the oriented apatite crystal is achieved by a vapor-solid growth mechanism, whereas lateral growth is suppressed by the graphitic layers formed through arrangement of the derived aromatic hydrocarbon molecules. We show that this unusual combination of the apatite crystal and the graphitic shells can lead to an excellent osteogenic differentiation and bony fusion through a programmed smart behavior. For instance, the graphitic shells are degraded after the initial cell growth promoted by the graphitic nanostructures, and the cells continue proliferation on the bare apatite nanowires. Furthermore, a bending experiment indicates that such core-shell nanowires exhibited a superior bending stiffness compared to single-crystal apatite nanowires without graphitic shells. The results suggest a new strategy and direction for bone grafting materials with a highly controllable morphology and material conditions that can best stimulate bone cell differentiation and growth. PMID:23755838

  15. Apatite-coated three-dimensional fibrous scaffolds and their osteoblast response.

    PubMed

    Tang, Yanwei; Zhao, Yan; Wong, Cynthia S; Wang, Xungai; Lin, Tong

    2013-03-01

    Apatite was applied onto the fiber surface of an interbonded three-dimensional polycaprolactone fibrous scaffold through a vacuum nitrogen plasma pretreatment followed by immersion in a simulated body fluid. The plasma pretreatment improved the wettability and accelerated apatite deposition on the fiber surface. The apatite coating was proven to be biocompatible to fibroblast cells without any cytotoxicity. Two osteoblast cell lines, human fetal osteoblast cells (hFOB1.19) and human osteosarcoma cells (Saos-2), were used for evaluating the cell response of the fibrous matrices. The apatite coating showed enhanced cell attachment for both hFOB1.19 and Saos-2 cells. In comparison to the uncoated fibrous scaffolds, the apatite-coated fibrous matrix had an improved hFOB1.19 cell proliferation for at least 2 weeks. Enhanced cell differentiation was also observed on the apatite-coated fibrous matrix primarily on the third, 10th, and 14th days of culture. Saos-2 cells showed improved proliferation in the apatite-coated matrix mainly on days 3 and 14, but the differentiation was increased only on the third day of culture. PMID:22941867

  16. Semiempirical electronic structure calculation on Ca and Pb apatites

    NASA Astrophysics Data System (ADS)

    Matos, Maria; Terra, Joice; Ellis, D. E.

    A systematic study is made on the electronic structure of stoichiometric calcium and lead apatites, using the tight binding extended Hückel method (eHT). The aim is to investigate the applicability of the semiempirical theory to study this family of compounds. A10(BO4)6X2 (A = Ca, Pb) apatites, differing by substitutions in the BO4 tetrahedral unit (B = P, As, and V) and X-channel ion (X = OH, Cl), are considered. The calculations show that eHT is suitable to describe basic properties especially concerning trends with atomic substitution and geometry changes. Band structure, Mulliken charge distribution, and bond orders are in good agreement with results of ab initio density functional theory (DFT) found in the literature. Large variations in the optical gap due to vanadium and lead substitutions are newly found. Changes in the anion X-channel affect the optical gap, which is in close agreement with DFT results. Analysis involving subnets are performed to determine the role of halogenic orbitals in the electronic structure of chloroapatites, showing evidence of covalent Cl bonding. It was also found that Pb=OH bonding in hydroxy-vanadinite Pb10(VO4)6(OH)2, recently synthesized, is weaker than that of Ca=OH in vanadate Ca10(VO4)6(OH)2. Arsenium is found to be more weakely bound to the O-tetrahedron than phosphorous, although Ca=O bond is increased with the substitution. We investigate, in addition, the electronic structure of a model system Ca10(AsO4)6(OH)2, obtained from direct As substitution in the vanadate Ca10(VO4)6(OH)2.

  17. Biomimetic magnesium-carbonate-apatite nanocrystals endowed with strontium ions as anti-osteoporotic trigger.

    PubMed

    Iafisco, Michele; Ruffini, Andrea; Adamiano, Alessio; Sprio, Simone; Tampieri, Anna

    2014-02-01

    The present work investigates the preparation of biomimetic nanocrystalline apatites co-substituted with Mg, CO3 and Sr to be used as starting materials for the development of nanostructured bio-devices for regeneration of osteoporotic bone. Biological-like amounts of Mg and CO3 ions were inserted in the apatite structure to mimic the composition of bone apatite, whereas the addition of increasing quantities of Sr ions, from 0 up to 12 wt.%, as anti-osteoporotic agent, was evaluated. The chemical-physical features, the morphology, the degradation rates, the ion release kinetics as well as the in vitro bioactivity of the as-prepared apatites were fully evaluated. The results indicated that the incorporation of 12 wt.% of Sr can be viewed as a threshold for the structural stability of Mg-CO3-apatite. Indeed, incorporation of lower quantity of Sr did not induce considerable variations in the chemical structure of Mg-CO3-apatite, while when the Sr doping extent reached 12 wt.%, a dramatically destabilizing effect was detected on the crystal structure thus yielding alteration of the symmetry and distortion of the PO4. As a consequence, this apatite exhibited the fastest degradation kinetic and the highest amount of Sr ions released when tested in physiological conditions. In this respect, the surface crystallization of new calcium phosphate phase when immersed in physiological-like solution occurred by different mechanisms and extents due to the different structural chemistry of the variously doped apatites. Nevertheless, all the apatites synthesized in this work exhibited in vitro bioactivity demonstrating their potential use to develop biomedical devices with anti-osteoporotic functionality. PMID:24411371

  18. Remediation of copper contaminated soil by using different particle sizes of apatite: a field experiment.

    PubMed

    Xing, Jinfeng; Hu, Tiantian; Cang, Long; Zhou, Dongmei

    2016-01-01

    The particle size of apatite is one of the critical factors that influence the adsorption of heavy metals on apatite in the remediation of heavy metal contaminated soils using apatite. However, little research has been done evaluating the impact of different particle sizes of apatite on immobilization remediation of heavy metal polluted soils in field. In this study, the adsorption isothermal experiments of copper on three kinds of apatite was tested, and the field experiment by using different particle sizes apatite [nano-hydroxyapatite (NAP), micro-hydroxyapatite (MAP), ordinary particle apatite (OAP)] at a same dosage of 25.8 t/ha (1.16 %, W/W) was also conducted. Ryegrass was chosen as the test plant. The ryegrass biomass, the copper contents in ryegrass and the copper fractionations in soil were determined after field experiments. Results of adsorption experiments showed that the adsorption amounts of copper on OAP was the lowest among different particles. The adsorption amounts of copper on MAP was higher than NAP at high copper equilibrium concentration (>1 mmol L(-1)), an opposite trend was obtained at low copper concentration (<1 mmol L(-1)). In the field experiment, we found that the application of different apatites could effectively increase the soil pH, decrease the available copper concentration in soil, provide more nutrient phosphate and promote the growth of ryegrass. The ryegrass biomass and the copper accumulation in ryegrass were the highest in MAP among all treatments. The effective order of apatite in phytoremediation of copper contaminated field soil was MAP > NAP > OAP, which was attributed to the high adsorption capacity of copper and the strong releasing of phosphate by MAP. PMID:27512641

  19. [Comparative studies on the material performances of natural bone-like apatite from different bone sources].

    PubMed

    Fan, Xiaoxia; Ren, Haohao; Chen, Shutian; Wang, Guangni; Deng, Tianyu; Chen, Xingtao; Yan, Yonggang

    2014-04-01

    The compressive strength of the original bone tissue was tested, based on the raw human thigh bone, bovine bone, pig bone and goat bone. The four different bone-like apatites were prepared by calcining the raw bones at 800 degrees C for 8 hours to remove organic components. The comparison of composition and structure of bone-like apatite from different bone sources was carried out with a composition and structure test. The results indicated that the compressive strength of goat bone was similar to that of human thigh bone, reached (135.00 +/- 7.84) MPa; Infrared spectrum (IR), X-ray diffraction (XRD) analysis results showed that the bone-like apatite from goat bone was much closer to the structure and phase composition of bone-like apatite of human bones. Inductively Coupled Plasma (ICP) test results showed that the content of trace elements of bone-like apatite from goat bone was closer to that of apatite of human bone. Energy Dispersive Spectrometer (EDS) results showed that the Ca/P value of bone-like apatite from goat bone was also close to that of human bone, ranged to 1.73 +/- 0.033. Scanning electron microscopy (SEM) patterns indicated that the macrographs of the apatite from human bone and that of goat bone were much similar to each other. Considering all the results above, it could be concluded that the goat bone-like apatite is much similar to that of human bone. It can be used as a potential natural bioceramic material in terms of material properties. PMID:25039141

  20. Adsorption of nucleotides on biomimetic apatite: The case of adenosine 5‧ monophosphate (AMP)

    NASA Astrophysics Data System (ADS)

    Hammami, K.; Feki, H. El; Marsan, O.; Drouet, C.

    2015-10-01

    This work investigates the interaction between the nucleotide adenosine 5‧ monophosphate molecule (AMP) and a biomimetic nanocrystalline carbonated apatite as a model for bone mineral. The analogy of the apatite phase used in this work with biological apatite was first pointed out by complementary techniques. AMP adsorption isotherms were then investigated. Obtained data were fitted to a Sips isotherm with an exponent greater than one suggesting positive cooperativity among adsorbed molecules. The data were compared to a previous study relative to the adsorption of another nucleotide, cytidine monophosphate (CMP) onto a similar substrate, evidencing some effect of the chemical nature of the nucleic base. An enhanced adsorption was observed under acidic (pH 6) conditions as opposed to pH 7.4, which parallels the case of DNA adsorption on biomimetic apatite. An estimated standard Gibbs free energy associated to the adsorption process (ΔG°ads ≅ -22 kJ/mol) intermediate between "physisorption" and "chemisorption" was found. The analysis of the solids after adsorption pointed to the preservation of the main characteristics of the apatite substrate but shifts or enhancements of Raman bands attributed to AMP showed the existence of chemical interactions involving both the phosphate and adenine parts of AMP. This contribution adds to the works conducted in view of better understanding the interaction of DNA/RNA and their constitutive nucleotides and the surface of biomimetic apatites. It could prove helpful in disciplines such as bone diagenesis (DNA/apatite interface in aged bones) or nanomedicine (setup of DNA- or RNA-loaded apatite systems). Also, the adsorption of nucleic acids on minerals like apatites could have played a role in the preservation of such biomolecules in the varying conditions known to exist at the origin of life on Earth, underlining the importance of dedicated adsorption studies.

  1. Exploiting radiation damage control on apatite (U Th)/He dates in cratonic regions

    NASA Astrophysics Data System (ADS)

    Flowers, Rebecca M.

    2009-01-01

    Apatites from four pairs of samples of Precambrian basement from the western Canadian shield were analyzed by (U-Th)/He thermochronometry to test for the influence of radiation damage on apatite (U-Th)/He dates in this cratonic region. Recent studies have demonstrated that the accumulation of radiation damage increases the apatite He retentivity, so that apatites with a span of effective U concentrations, eU, that experienced the same thermal history may be characterized by a range of closure temperatures. In this investigation, each sample pair consisted of a mafic dike cross-cutting felsic gneisses from a single outcrop or nearby outcrops that contained apatites with a span of eU. The apatites yielded (U-Th)/He dates from 846 to 123 Ma, and were positively correlated with eU within each sample pair. These results can be explained using a model that tracks the evolution of He mobility in response to the accumulation of radiation damage. When coupled with regional geological constraints, the data appear to require partial to complete He loss due to burial and reheating in Phanerozoic time. New apatite fission- track dates and length data were obtained for five of these samples. The apatite fission- track dates are Proterozoic regardless of apatite eU. Thermal history simulations indicate that the apatite fission-track data are compatible with the (U-Th)/He results, although the thermal histories are not identical in detail and the fission-track results alone do not require Phanerozoic heating. Together the data are consistent with burial of this region by ≥ 1 km of Phanerozoic strata that were subsequently denuded, thus pointing toward significant Phanerozoic deposition in the North American cratonic interior hundreds of kilometers east of where previously documented. The results suggest that exploiting radiation damage control on apatite (U-Th)/He dates through investigation of surface sample apatites with a span of closure temperatures can impose tighter

  2. Synthesis, characterization and electrical properties of a lead sodium vanadate apatite

    SciTech Connect

    Chakroun-Ouadhour, E.; Ternane, R. Hassen-Chehimi, D. Ben; Trabelsi-Ayadi, M.

    2008-08-04

    The lacunary lead sodium vanadate apatite Pb{sub 8}Na{sub 2}(VO{sub 4}){sub 6} was synthesized by the solid-state reaction method. The compound was characterized by X-ray powder diffraction, infrared (IR) absorption spectroscopy and Raman scattering spectroscopy. By comparing the effect of vanadate and phosphate ions on electrical properties, it was concluded that Pb{sub 8}Na{sub 2}(VO{sub 4}){sub 6} apatite is better conductor than Pb{sub 8}Na{sub 2}(PO{sub 4}){sub 6} apatite.

  3. Quantification of octacalcium phosphate, authigenic apatite and detrital apatite in coastal sediments using differential dissolution and standard addition

    NASA Astrophysics Data System (ADS)

    Oxmann, J. F.; Schwendenmann, L.

    2014-06-01

    Knowledge of calcium phosphate (Ca-P) solubility is crucial for understanding temporal and spatial variations of phosphorus (P) concentrations in water bodies and sedimentary reservoirs. In situ relationships between liquid- and solid-phase levels cannot be fully explained by dissolved analytes alone and need to be verified by determining particular sediment P species. Lack of quantification methods for these species limits the knowledge of the P cycle. To address this issue, we (i) optimized a specifically developed conversion-extraction (CONVEX) method for P species quantification using standard additions, and (ii) simultaneously determined solubilities of Ca-P standards by measuring their pH-dependent contents in the sediment matrix. Ca-P minerals including various carbonate fluorapatite (CFAP) specimens from different localities, fluorapatite (FAP), fish bone apatite, synthetic hydroxylapatite (HAP) and octacalcium phosphate (OCP) were characterized by XRD, Raman, FTIR and elemental analysis. Sediment samples were incubated with and without these reference minerals and then sequentially extracted to quantify Ca-P species by their differential dissolution at pH values between 3 and 8. The quantification of solid-phase phosphates at varying pH revealed solubilities in the following order: OCP > HAP > CFAP (4.5% CO3) > CFAP (3.4% CO3) > CFAP (2.2% CO3) > FAP. Thus, CFAP was less soluble in sediment than HAP, and CFAP solubility increased with carbonate content. Unspiked sediment analyses together with standard addition analyses indicated consistent differential dissolution of natural sediment species vs. added reference species and therefore verified the applicability of the CONVEX method in separately determining the most prevalent Ca-P minerals. We found surprisingly high OCP contents in the coastal sediments analyzed, which supports the hypothesis of apatite formation by an OCP precursor mechanism.

  4. Using Oxygen Isotopes in Fish Scale Apatite to Reconstruct Past Temperatures and Water Isotope Ratios

    NASA Astrophysics Data System (ADS)

    Lambert, T. D.; Paytan, A.

    2009-12-01

    Oxygen isotope ratios (δ18O) of apatite phosphate in fish bones and teeth vary according to the temperature and δ18O of water during formation. Since isotope ratios in apatite are often well preserved over geologic timescales, fish bones and teeth have been used to determine past environmental conditions. Fish scales offer several advantages over bones and teeth: they are relatively common in certain sedimentary basins, and they are more easily identified to species level. Analysis of paired bone and scale samples will be presented. The data indicate that fish scale apatite similarly records environmental conditions during growth. Thus δ18O of apatite phosphate in fish scales may provide useful paleoecological information and also indicate past environmental conditions.

  5. In Situ Formation of Calcium Apatite in Soil for Sequestering Contaminants in Soil and Groundwater

    SciTech Connect

    Moore, Robert; Szecsody, Jim; Thompson, Mike

    2015-10-20

    A new method for in situ formation of a calcium apatite permeable reactive barrier that is a groundbreaking technology for containing radioactive/heavy metal contaminants threatening groundwater supplies.

  6. Dissolution mechanism of calcium apatites in acids: A review of literature

    PubMed Central

    Dorozhkin, Sergey V

    2012-01-01

    Eight dissolution models of calcium apatites (both fluorapatite and hydroxyapatite) in acids were drawn from the published literature, analyzed and discussed. Major limitations and drawbacks of the models were conversed in details. The models were shown to deal with different aspects of apatite dissolution phenomenon and none of them was able to describe the dissolution process in general. Therefore, an attempt to combine the findings obtained by different researchers was performed which resulted in creation of the general description of apatite dissolution in acids. For this purpose, eight dissolution models were assumed to complement each other and provide the correct description of the specific aspects of apatite dissolution. The general description considers all possible dissolution stages involved and points out to some missing and unclear phenomena to be experimentally studied and verified in future. This creates a new methodological approach to investigate reaction mechanisms based on sets of affine data, obtained by various research groups under dissimilar experimental conditions. PMID:25237611

  7. Fluoride enhances transfection activity of carbonate apatite by increasing cytoplasmic stability of plasmid DNA

    SciTech Connect

    Chowdhury, E.H.

    2011-06-17

    Highlights: {yields} Cytoplasmic stability of plasmid DNA is enhanced by fluoride incorporation into carbonate apatite carrier. {yields} Fluoridated carbonate apatite promotes a robust increase in transgene expression. {yields} Controlled dissolution of fluoridated carbonate apatite in endosomal acidic environment might buffer the endosomes and prevent degradation of the released DNA. -- Abstract: Intracellular delivery of a functional gene or a nucleic acid sequence to specifically knockdown a harmful gene is a potential approach to precisely treat a critical human disease. The intensive efforts in the last few decades led to the development of a number of viral and non-viral synthetic vectors. However, an ideal delivery tool in terms of the safety and efficacy has yet to be established. Recently, we have developed pH-sensing inorganic nanocrystals of carbonate apatite for efficient and cell-targeted delivery of gene and gene-silencing RNA. Here we show that addition of very low level of fluoride to the particle-forming medium facilitates a robust increase in transgene expression following post-incubation of the particles with HeLa cells. Confocal microscopic observation and Southern blotting prove the cytoplasmic existence of plasmid DNA delivered by likely formed fluoridated carbonate apatite particles while degradation of plasmid DNA presumably by cytoplasmic nucleases was noticed following delivery with apatite particles alone. The beneficial role of fluoride in enhancing carbonate apatite-mediated gene expression might be due to the buffering potential of generated fluoridated apatite in endosomal acidic environment, thereby increasing the half-life of delivered plasmid DNA.

  8. Chitosan reinforced apatite-wollastonite coating by electrophoretic deposition on titanium implants.

    PubMed

    Sharma, Smriti; Soni, Vivek P; Bellare, Jayesh R

    2009-07-01

    A novel bioactive porous apatite-wollastonite/chitosan composite coating was prepared by electrophoretic deposition. The influence of synthesis parameters like pH of suspension and current density was studied and optimized. X-ray diffraction confirmed crystalline phase of apatite-wollastonite in powder as well as composite coating with coat crystallinity of 65%. Scanning electron microscope showed that the porosity had interconnections with good homogeneity between the phases. The addition of chitosan increased the adhesive strength of the composite coating. Young's modulus of the coating was found to be 9.23 GPa. One of our key findings was sheet-like apatite growth unlike ball-like growth found in bioceramics. Role of chitosan was studied in apatite growth mechanism in simulated body fluid. In presence of chitosan, dense negatively charged surface with homogenous nucleation was the primary factor for sheet-like evolution of apatite layer. The results suggest that incorporation of chitosan with apatite-wollastonite in composite coating could provide excellent in vitro bioactivity with enhanced mechanical properties. PMID:19253015

  9. The lanthanides and yttrium in minerals of the apatite group; a review

    USGS Publications Warehouse

    Fleischer, Michael; Altschuler, Z.S.

    1982-01-01

    More than 1000 analyses have been tabulated of the distribution of the lanthanides and yttrium in minerals of the apatite group, recalculated to atomic percentages. Average compositions have been calculated for apatites from 14 types of rocks. These show a progressive change of composition from apatites of granitic pegmatites, highest in the heavy lanthanides and yttrium, to those from alkalic pegmatites, highest in the light lanthanides and lowest in yttrium. This progression is clearly shown in plots of S (= at % La+Ce+Pr) vs the ratio La/Nd and of S vs the ratio 100Y/(Y+Ln), where Ln is the sum of the lanthanides. Apatites of sedimentary phosphorites occupy a special position, being relatively depleted in Ce and relatively enriched in yttrium and the heavy lanthanides, consequences of deposition from sea water. Apatites associated with iron ores are close in composition to apatites of carbonatites, alkalic ultramafic, and ultramafic rocks, being enriched in the light lanthanides and depleted in the heavy lanthanides. Their compositions do not support the hypothesis of Parak that the Kiruna-type ores are of sedimentary origin. Table 9 and Figures 1-3 show the dependence of lanthanide distribution on the nature of the host rock. Although a given analysis of the lanthanides does not unequivocally permit certain identification of the host rock, it can indicate a choice of highly probable host rocks.

  10. Combined apatite fission track and U-Pb dating by LA-ICPMS

    NASA Astrophysics Data System (ADS)

    Chew, D. M.; Donelick, R. A.

    2012-04-01

    Apatite is a common accessory mineral in igneous, metamorphic and clastic sedimentary rocks. It is a nearly ubiquitous accessory phase in igneous rocks, is common in metamorphic rocks of pelitic, carbonate, basaltic, and ultramafic composition and is virtually ubiquitous in clastic sedimentary rocks. In contrast to the polycyclic behavior of the stable heavy mineral zircon, apatite is unstable in acidic groundwaters and has limited mechanical stability in sedimentary transport systems. Apatite has many potential applications in provenance studies, particularly as it likely represents first-cycle detritus. Fission track and U-Pb dating are very powerful techniques in apatite provenance studies. They yield complementary information, with the apatite fission-track system yielding low-temperature exhumation ages and the U-Pb system yielding high-temperature cooling ages which constrain the timing of apatite crystallization. This study focuses on integrating apatite fission track and U-Pb dating by the LA-ICPMS method. Our approach is intentionally broad in scope, and is applicable to any quadrupole or rapid-scanning magnetic-sector LA-ICPMS system. Calculating uranium concentrations in fission-track dating by LA-ICPMS increases the speed of analysis and sample throughput compared to the conventional external detector method and avoids the need for neutron irradiation (Hasebe et al., 2004). LA-ICPMS-based uranium measurements in apatite are measured relative to an internal concentration standard (typically 43Ca). Ca in apatite is not always stochiometric as minor cations (Mn2+, Sr2+, Ba2+ and Fe2+) and REE can substitute with Ca2+. These substitutions must be quantified by multi-elemental LA-ICPMS analyses. Such data are also useful for discriminating between different apatite populations in sedimentary or volcaniclastic rocks based on their trace-element chemistry. Low U, Th and radiogenic Pb concentrations, elevated common Pb / radiogenic Pb ratios and U-Pb elemental

  11. Treatability of organic matter derived from surface and subsurface waters of drinking water catchments.

    PubMed

    Awad, John; van Leeuwen, John; Liffner, Joel; Chow, Christopher; Drikas, Mary

    2016-02-01

    The treatability of NOM present in runoff and subsurface waters from discrete zero-order catchments (ZOCs) with three land management practices (Australian native vegetation, pine plantation, grasslands) on varying soil textures of a closed drinking water reservoir-catchment was investigated. Subsurface water samples were collected by lysimeters and shallow piezometers and surface waters by installation of barriers that diverted waters to collection devices. For small sample volumes collected, a 'micro' jar testing procedure was developed to assess the treatability of organics by enhanced coagulation using alum, under standardised conditions. DOM present in water samples was quantified by measurement of DOC and UV absorbance (at 254 nm) and characterized using these and F-EEM. The mean alum dose rate (mg alum per mg DOC removed or Al/DOC) was found to be lower for DOM from sandy soil ZOCs (21.1 ± 11.0 Al/DOC) than from clayey soil ZOCs (38.6 ± 27.7 Al/DOC). ZOCs with Pinus radiata had prominent litter layers (6.3 ± 2.6 cm), and despite differences in soil textures showed similarity in DOM character in subsurface waters, and in alum dose rates (22.2 ± 5.5 Al/DOC). For sandy soil ZOCs, the lowest alum dose rates (16.5 ± 10.6 Al/DOC) were for waters from native vegetation catchment while, for clayey soil ZOCs, waters from pine vegetation had the lowest alum dose rates (23.0 ± 5.0 Al/DOC). Where ZOCs have a prominent O horizon, soil minerals had no apparent influence on the treatability of DOM. PMID:26461444

  12. Demonstration testing and evaluation of in situ soil heating. Treatability study work plan, Revision 1

    SciTech Connect

    Sresty, G.C.

    1994-07-07

    A Treatability Study planned for the demonstration of the in situ electromagnetic (EM) heating process to remove organic solvents is described in this Work Plan. The treatability study will be conducted by heating subsurface vadose-zone soils in an organic plume adjacent to the Classified Burial Ground K-1070-D located at K-25 Site, Oak Ridge. The test is scheduled to start during the fourth quarter of FY94 and will be completed during the first quarter of FY95. The EM heating process for soil decontamination is based on volumetric heating technologies developed during the `70s for the recovery of fuels from shale and tar sands by IIT Research Institute (IITRI) under a co-operative program with the US Department of Energy (DOE). Additional modifications of the technology developed during the mid `80s are currently used for the production of heavy oil and waste treatment. Over the last nine years, a number of Government agencies (EPA, Army, AF, and DOE) and industries sponsored further development and testing of the in situ heating and soil decontamination process for the remediation of soils containing hazardous organic contaminants. In this process the soil is heated in situ using electrical energy. The contaminants are removed from the soil due to enhanced vaporization, steam distillation and stripping. IITRI will demonstrate the EM Process for in situ soil decontamination at K-25 Site under the proposed treatability study. Most of the contaminants of concern are volatile organics which can be removed by heating the soil to a temperature range of 85 to 95 C. The efficiency of the treatment will be determined by comparing the concentration of contaminants in soil samples. Samples will be obtained before and after the demonstration for a measurement of the concentration of contaminants of concern.

  13. Final waste forms project: Performance criteria for phase I treatability studies

    SciTech Connect

    Gilliam, T.M.; Hutchins, D.A.; Chodak, P. III

    1994-06-01

    This document defines the product performance criteria to be used in Phase I of the Final Waste Forms Project. In Phase I, treatability studies will be performed to provide {open_quotes}proof-of-principle{close_quotes} data to establish the viability of stabilization/solidification (S/S) technologies. This information is required by March 1995. In Phase II, further treatability studies, some at the pilot scale, will be performed to provide sufficient data to allow treatment alternatives identified in Phase I to be more fully developed and evaluated, as well as to reduce performance uncertainties for those methods chosen to treat a specific waste. Three main factors influence the development and selection of an optimum waste form formulation and hence affect selection of performance criteria. These factors are regulatory, process-specific, and site-specific waste form standards or requirements. Clearly, the optimum waste form formulation will require consideration of performance criteria constraints from each of the three categories. Phase I will focus only on the regulatory criteria. These criteria may be considered the minimum criteria for an acceptable waste form. In other words, a S/S technology is considered viable only if it meet applicable regulatory criteria. The criteria to be utilized in the Phase I treatability studies were primarily taken from Environmental Protection Agency regulations addressed in 40 CFR 260 through 265 and 268; and Nuclear Regulatory Commission regulations addressed in 10 CFR 61. Thus the majority of the identified criteria are independent of waste form matrix composition (i.e., applicable to cement, glass, organic binders etc.).

  14. Treatability studies of alternative wastewaters for Metal Finishing Effluent Treatment Facility

    SciTech Connect

    Wittry, D.M.; Martin, H.L.

    1994-06-01

    The 300-M Area Liquid Effluent Treatment Facility (LETF) of the Savannah River Site (SRS) is an end-of-pipe industrial wastewater treatment facility that uses precipitation and filtration, which is the EPA Best Available Technology economically achievable for a Metal Finishing and Aluminum Form Industries. Upon the completion of stored waste treatment, the LETF will be shut down, because production of nuclear materials for reactors stopped at the end of the Cold War. The economic use of the LETF for the treatment of alternative wastewater streams is being evaluated through laboratory bench-scale treatability studies.

  15. Borehole Data Package for Nine CY 2006 Polyphosphate Treatability Testing Wells, 300-FF-5 Operable Unit, Hanford Site, Washington

    SciTech Connect

    Williams, Bruce A.

    2007-04-12

    Nine new CERCLA groundwater monitoring wells were installed in the 300-FF-5 Operable Unit in calendar year 2006 to fulfill commitments for the EM-20 funded polyphosphate treatability test. Nine new performance monitoring wells were drilled into the uppermost unconfined aquifer, to the Hanford formation - Ringold Formation contact boundary, and completed within the permeable Hanford fm. unit 1 gravel-dominated sequence. The overall objective of the polyphosphate treatability test is to evaluate the efficacy of using polyphosphate injections to treat 300 Area uranium contaminated groundwater in situ. The objective of this work was to install the performance monitoring network surrounding the existing treatability injection well C5000 (399-1-23) in support of the implementation of a field scale demonstration of the polyphosphate technology.

  16. Interrogating the Effects of Radiation Damage Annealing on Helium Diffusion Kinetics in Apatite

    NASA Astrophysics Data System (ADS)

    Willett, C. D.; Fox, M.; Shuster, D. L.

    2015-12-01

    Apatite (U-Th)/He thermochronology is commonly used to study landscape evolution and potential links between climate, erosion and tectonics. The technique relies on a quantitative understanding of (i) helium diffusion kinetics in apatite, (ii) an evolving 4He concentration, (iii) accumulating damage to the crystal lattice caused by radioactive decay[1], and (iv) the thermal annealing of such damage[2],[3], which are each functions of both time and temperature. Uncertainty in existing models of helium diffusion kinetics has resulted in conflicting conclusions, especially in settings involving burial heating through geologic time. The effects of alpha recoil damage annealing are currently assumed to follow the kinetics of fission track annealing (e.g., reference [3]), although this assumption is difficult to fully validate. Here, we present results of modeling exercises and a suite of experiments designed to interrogate the effects of damage annealing on He diffusivity in apatite that are independent of empirical calibrations of fission track annealing. We use the existing experimental results for Durango apatite[2] to develop and calibrate a new function that predicts the effects of annealing temperature and duration on measured diffusivity. We also present a suite of experiments conducted on apatite from Sierra Nevada, CA granite to establish whether apatites with different chemical compositions have the same behavior as Durango apatite. Crystals were heated under vacuum to temperatures between 250 and 500°C for 1, 10, or 100 hours. The samples were then irradiated with ~220 MeV protons to produce spallogenic 3He, the diffusant then used in step-heating diffusion experiments. We compare the results of these experiments and model calibrations to existing models. Citations: [1]Shuster, D., Flowers R., and Farley K., (2006), EPSL 249(3-4), 148-161; [2]Shuster, D. and Farley, K., (2009), GCA 73 (1), 6183-6196; [3]Flowers, R., Ketcham, R., Shuster, D. and Farley, K

  17. Adsorption and release of amino acids mixture onto apatitic calcium phosphates analogous to bone mineral

    NASA Astrophysics Data System (ADS)

    El Rhilassi, A.; Mourabet, M.; El Boujaady, H.; Bennani-Ziatni, M.; Hamri, R. El; Taitai, A.

    2012-10-01

    Study focused on the interaction of adsorbate with poorly crystalline apatitic calcium phosphates analogous to bone mineral. Calcium phosphates prepared in water-ethanol medium at physiological temperature (37 °C) and neutral pH, their Ca/P ratio was between 1.33 and 1.67. Adsorbate used in this paper takes the mixture form of two essential amino acids L-lysine and DL-leucine which have respectively a character hydrophilic and hydrophobic. Adsorption and release are investigated experimentally; they are dependent on the phosphate type and on the nature of adsorbate L-lysine, DL-leucine and their mixture. Adsorption of mixture of amino acids on the apatitic calcium phosphates is influenced by the competition between the two amino acids: L-lysine and DL-leucine which exist in the medium reaction. The adsorption kinetics is very fast while the release kinetics is slow. The chemical composition of apatite has an influence on both adsorption and release. The interactions adsorbate-adsorbent are electrostatic type. Adsorption and release reactions of the amino acid mixture are explained by the existence of the hydrated surface layer of calcium phosphate apatite. The charged sbnd COOsbnd and sbnd NH3+ of adsorbates are the strongest groups that interact with the surface of apatites, the adsorption is mainly due to the electrostatic interaction between the groups sbnd COOsbnd of amino acids and calcium Ca2+ ions of the apatite. Comparative study of interactions between adsorbates (L-lysine, DL-leucine and their mixture) and apatitic calcium phosphates is carried out in vitro by using UV-vis and infrared spectroscopy IR techniques.

  18. Aerobic treatability of waste effluent from the leather finishing industry. Master's thesis

    SciTech Connect

    Vinger, J.A.

    1993-12-01

    The Seton Company supplies finished leather products exclusively for the automotive industry. In the process of finishing leather, two types of wastewaters are generated. The majority of the wastewater is composed of water-based paint residuals while the remainder is composed of solvent-based coating residuals. Aerobic treatability studies were conducted using water-based and solvent-based waste recirculatory waters from the Seton Company's Saxton, Pennsylvania processing plant. The specific objective was to determine the potential for using aerobic biological processes to biodegrade the industry's wastes and determine the potential for joint treatment at the local publicly owned treatment works (POTW). This study was accomplished in two phases. Phase I was conducted during the Spring Semester 1993 and consisted of aerobic respirometer tests of the raw wastes and mass balance analysis. The results of Phase I were published in a report to the Seton Company as Environmental Resources Research Institute project number 92C.II40R-1. Phase II was conducted during the Summer Semester 1993 and consisted of bench-scale reactor tests and additional aerobic respirometer tests. The aerobic respirometer batch tests and bench-scale reactor tests were used to assess the treatability of solvent-based and water-based wastewaters and determine the degree of biodegradability of the wastewaters. Mass balance calculations were made using measured characteristics.

  19. Treatability of TCE-contaminated clay soils at the Rinsewater Impoundment, Michoud Assembly Facility

    SciTech Connect

    Lucero, A.J.; Gilbert, V.P.; Hewitt, J.D.; Koran, L.J. Jr.; Jennings, H.L.; Donaldson, T.L.; West, O.R.; Cline, S.R.; Marshall, D.S.

    1995-02-01

    The Oak Ridge National Laboratory has conducted treatability studies on clay soils taken from the Rinsewater Impoundment at the National Aeronautics and Space Administration Michoud Assembly Facility. The soils are contaminated with up to 3000 mg/kg of trichloroethylene and cis-1,2-dichloroethylene, less than 10 mg/kg of trans-1,2-DCE, and less than 10 mg/kg of vinyl chloride. The goal of the study described in this report was to identify and test in situ technologies and/or develop a modified treatment regime to remove or destroy volatile organic compounds from the contaminated clay soils. Much of the work was based upon previous experience with mixed-region vapor stepping and mixed-region peroxidation. Laboratory treatments were performed on intact soil cores that were taken from contaminated areas at the Rinsewater Impoundment at MAF. Treatability studies were conducted on soil that was close to in situ conditions in terms of soil structure and contaminant concentrations.

  20. Decomposition of PCBs in oils using gamma radiolysis: A treatability study. Final report

    SciTech Connect

    Mincher, B.J.; Arbon, R.E.

    1996-04-01

    This report presents the results of a treatability study of radiologically and PCB contaminated waste hydraulic oils at the Idaho National Engineering Laboratory (INEL). The goal of the study was to demonstrate that PCBs could be selectively removed from the contaminated oils. The PCBs were selectively decomposed in an in-situ fashion via gamma-ray radiolysis. The gamma-ray source was spent nuclear fuel at the Advanced Test Reactor (ATR) canal at the Test Reactor Area (TRA), of the INEL. Exposure to gamma-rays does not induce radioactivity in the exposed solutions. The treatability study was the culmination of five years of research concerning PCB radiolysis conducted at INEL which investigated the mechanism and kinetics of the reaction in several solvents. The major findings of this research are summarized here. Based upon these findings three INEL waste streams were selected for testing of the process. The Environmental Protection Agency (EPA) treatment standard of 2 mg/kg was successfully achieved in all waste streams. The interference of contaminants other than PCBs is discussed.

  1. Characterization and photocatalytic treatability of red water from Brazilian TNT industry.

    PubMed

    Ludwichk, Raquel; Helferich, Oliver Karil; Kist, Cristiane Patrícia; Lopes, Aline Chitto; Cavasotto, Thiago; Silva, Davi Costa; Barreto-Rodrigues, Marcio

    2015-08-15

    The current study aims to characterize and evaluate the photocatalytic treatability of the "red water" effluent from a Brazilian TNT production industry. Analyses were performed using physical, chemical, spectroscopic and chromatographic assays, which demonstrated that the effluent presented a significant pollution potential, mainly due to COD, BOD, solids and to the high concentration of nitroaromatic compounds such as 1,3,5-trinitrobenzene, 1-methyl-2,4-dinitrobenzene, 2-methyl-1,3-dinitrobenzene, 2,4,6-trinitrotoluene-3,5-dinitro-p-toluidine and 2-methyl-3,5-dinitro-benzoamine. By a modified sol-gel and a dip-coating technique, it was possible to obtain a TiO2 film on borosilicate glass substrate which functional composition and microstructure were characterized by infrared spectroscopy and scanning electron microscopy. The evaluation of the photocatalytic treatability using borosilicate-glass-TiO2 demonstrated high degradation efficiency. In this context, a reduction of 32 and 100% for COD and nitroaromatic compounds, respectively, was observed. Although the proposed photocatalytic process has found difficulties in reducing the content of organic matter and effluent color in the red water, its potential for degrading refractory chemical compounds such as the nitroaromatic ones enables it to be used as tertiary treatment. PMID:25827271

  2. Analytically oriented psychotherapy in schizotypal and borderline patients: at the border of treatability.

    PubMed Central

    Stone, M. H.

    1985-01-01

    Analytically oriented psychotherapy (AOP) has been considered the treatment of choice for borderline patients and a useful technique in the treatment of schizotypal patients. There are many exceptions, however, in addition to a number of borderline and schizotypal patients who are just barely amenable to this modality: they are at the border of treatability by AOP. Limitations relating to time, cost, and the availability of therapists trained in this discipline render it important to delineate the factors which conduce either to the success or failure of AOP. From the author's clinical impressions about borderline and schizotypal patients at the border of treatability by AOP, a number of such factors emerge. On the positive side: likeableness, autoplastic defenses, high motivation, psychological-mindedness, genuine concern, good moral sense, self-discipline, and low impulsivity. Negative factors include, beside the opposites to the aforementioned, vengefulness and parental abusiveness or exploitation. A scale for measuring the balance between these positive and negative factors is proposed. Its use may, it is hoped, improve forecast, during initial consultation, as to which borderline and schizotypal patients will respond favorably to AOP. PMID:4049910

  3. TREATABILITY TEST REPORT FOR THE REMOVAL OF CHROMIUM FROM GROUNDWATER AT 100-D AREA USING ELECTROCOAGULATION

    SciTech Connect

    PETERSEN SW

    2009-09-24

    The U.S. Department of Energy (DOE) has committed to accelerate cleanup of contaminated groundwater along the Columbia River. The current treatment approach was driven by a series of Interim Action Records of Decision (IAROD) issued in the mid-1990s. Part of the approach for acceleration involves increasing the rate of groundwater extraction for the chromium plume north of the 100-D Reactor and injecting the treated water in strategic locations to hydraulically direct contaminated groundwater toward the extraction wells. The current treatment system uses ion exchange for Cr(VI) removal, with off-site regeneration of the ion exchange resins. Higher flow rates will increase the cost and frequency of ion exchange resin regeneration; therefore, alternative technologies are being considered for treatment at high flow rates. One of these technologies, electrocoagulation (EC), was evaluated through a pilot-scale treatability test. The primary purpose of the treatability study was to determine the effectiveness of Cr(VI) removal and the robustness/implementability of an EC system. Secondary purposes of the study were to gather information about derivative wastes and to obtain data applicable to scaling the process from the treatability scale to full-scale. The treatability study work plan identified a performance objective and four operational objectives. The performance objective for the treatability study was to determine the efficiency (effectiveness) of hexavalent chromium removal from the groundwater, with a desired concentration of {le} 20 micrograms per liter ({micro}g/L) Cr(VI) in the effluent prior to re-injection. Influent and effluent total chromium and hexavalent chromium data were collected using a field test kit for multiple samples per week, and from off-site laboratory analysis of samples collected approximately monthly. These data met all data quality requirements. Two of three effluent chromium samples analyzed in the off-site (that is, fixed) laboratory

  4. Magnetite-apatite mineralization in Khanlogh iron deposit, northwest of Neyshaboor, NE Iran

    NASA Astrophysics Data System (ADS)

    Najafzadeh Tehrani, Parvin; Asghar Calagari, Ali; Velasco Roldan, Francisco; Simmonds, Vartan; Siahcheshm, Kamal

    2016-04-01

    Khanlogh iron deposit lies on Sabzehvar-Ghoochan Cenozoic magmatic belt in northwest of Neyshaboor, NE Iran. The lithologic units in this area include a series of sub-volcanic intrusive rocks like diorite porphyry, quartz-diorite porphyry, and micro-granodiorite of Oligocene age. Mineralization in this area occurred as veins, dissemination, and open space filling in brecciated zones within the host sub-volcanic intrusive bodies. Three distinct types of mineral associations can be distinguished, (1) diopside-magnetite, (2) magnetite-apatite, and (3) apatite-calcite. Microscopic examinations along with SEM and EPMA studies demonstrated that magnetite is the most common ore mineral occurring as solitary crystals. The euhedral magnetite crystals are accompanied by lamellar destabilized ilmenite and granular fluorapatite in magnetite-apatite ores. The results of EPMA revealed that the lamellar ilmenite, relative to host magnetite crystal, is notably enriched in MgO and MnO (average of 3.3 and 2.6 wt%, respectively; n=5), whereas magnetite is slighter enriched in Ti (TiO2 around 1.8 wt%) being average of MgO, MnO and V2O3 of 0.6wt%, 0.2wt%, and 0.6 wt% (respectively; n=20). Minerals such as chlorapatite, calcite, and chalcedony are also present in the magnetite-apatite ores. The samples from apatite-calcite ores contain coarse crystals of apatite and rhomboedral calcite. The plot of the EPMA data of Khanlogh iron ore samples on diagram of TiO2-V2O5 (Hou et al, 2011) illustrated that the data points lies between the well-known Kiruna and El Laco (Chile) iron deposits. The magnetite crystals in the sub-volcanic host rocks were possibly formed by immiscible iron oxide fluids during magmatic stage. However, the magnetite and apatite existing in the veins and breccia zones may have developed by high temperature hydrothermal fluids. Studies done by Purtov and Kotelnikova (1993) proved that the proportion of Ti in magnetite is related to fluoride complex in the hydrothermal

  5. Apatite formation behaviour during metasomatism in the Bathtub Intrusion (Babbitt deposit, Duluth Complex, USA)

    NASA Astrophysics Data System (ADS)

    Raič, Sara; Mogessie, Aberra; Krenn, Kurt; Hauzenberger, Christoph A.; Tropper, Peter

    2016-04-01

    The mineralized troctolitic Bathtub intrusion (Duluth Complex, NE-Minnesota) is known for its famous Cu-Ni-Sulfide±PGM Babbitt deposit, where platinum group minerals (PGMs) are either hosted by primary magmatic sulfides (base metal sulfides) or associated with hydrothermally altered portions. This secondary generation of PGMs is present in alteration patches and suggests the involvement of hydrothermal fluids in the mobilization of platinum-group elements (PGEs). Accessory fluorapatite in these samples reveals besides H2O- and CO2-rich primary fluid inclusions, textural and compositional variations that also record magmatic and metasomatic events. Based on detailed back-scattered electron imaging (BSE) and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICPMS), a primary magmatic origin is reflected by homogeneous or zoned grains, where zoning patterns are either concentric or oscillatory, with respect to LREE. Late magmatic to hydrothermal processes are indicated by grains with bright LREE-enriched rims or conversion textures with REE-enriched patches in the interior of the apatite. A metasomatic formation of monazite from apatite is documented by the presence of monazite inclusions in apatite and newly grown monazite at altered apatite rims. They formed by the release of REEs from the apatite during a fluid-induced alteration, based on the coupled substitution Ca2+ + P5+ = REE3+ + Si4+ (Rønsbo 1989; Rønsbo 2008). Samples with monazite inclusions in apatite further display occurrences of PGMs associated with hydrothermal alteration patches (chlorite + amphibole). The presence of H2O- and CO2-rich fluid inclusions in apatite, the metasomatically induced monazite growth, as well as the occurrence of PGMs in hydrothermally alteration zones, also suggest the involvement of aqueous chloride complexes in a H2O dominated fluid in the transportation of LREE and redistribution of the second generation of PGEs. Rønsbo, J.G. (1989): Coupled substitutions

  6. Apatite-forming ability of a zirconia/alumina nano-composite induced by chemical treatment.

    PubMed

    Uchida, Masaki; Kim, Hyun-Min; Kokubo, Tadashi; Nawa, Masahiro; Asano, Taiyo; Tanaka, Kenji; Nakamura, Takashi

    2002-05-01

    Induction of an apatite-forming ability on a nano-composite of a ceria-stabilized tetragonal zirconia polycrystals (Ce-TZP) and alumina (Al2O3) polycrystals via chemical treatment with aqueous solutions of H3PO4, H2SO4, HCl, or NaOH has been investigated. The Ce-TZP/Al2O3 composite is attractive as a load-bearing bone substitute because of its mechanical properties. The chemical treatments produced Zr-OH surface functional groups, which are known to be effective for apatite nucleation in a body environment. The composite, after chemical treatment, was shown to form a bonelike apatite layer when immersed in a simulated body fluid containing ion concentrations nearly equal to those in human blood plasma. This implies that it may form apatite in the living body and bond to living bone through the apatite layer. This type of bioactive Ce-TZP/Al2O3 composite is therefore expected to be useful as a bone substitute, even under load-bearing conditions. PMID:11857434

  7. Bioactive bredigite coating with improved bonding strength, rapid apatite mineralization and excellent cytocompatibility.

    PubMed

    Yi, Deliang; Wu, Chengtie; Ma, Bing; Ji, Heng; Zheng, Xuebin; Chang, Jiang

    2014-05-01

    Previous studies have shown that bredigite (Ca7MgSi4O16) bioceramics possessed excellent biocompatibility, apatite-mineralization ability and mechanical properties. In this paper, the bredigite coating on Ti-6Al-4 V substrate was prepared by plasma spraying technique. The main compositions of the coating were bredigite crystal phase with small parts of amorphous phases. The bonding strength of the coating to Ti-6Al-4 V substrate reached 49.8 MPa, which was significantly higher than that of hydroxyapatite coating and other silicate-based bioceramic coatings prepared by same method. After immersed in simulated body fluid for 2 days, a distinct apatite layer was deposited on the surface of bredigite coating, indicating that the prepared bredigite coating has excellent apatite-mineralization ability. The prepared bredigite coating supported the attachment and proliferation of rabbit bone marrow stem cells. The proliferation level of bone marrow stem cells was significantly higher than that on the hydroxyapatite coating. Our further study showed that the released SiO4 (4-) and Mg(2+) ions from bredigite coating as well as the formed nano-apatite layer on the coating surface might mainly contribute to the improvement of cell proliferation. The results indicated that the bredigite coating may be applied on orthopedic implants due to its excellent bonding strength, apatite mineralization and cytocompatibility. PMID:24131918

  8. Oleate adsorption at an apatite surface studied by ex-situ FTIR internal reflection spectroscopy

    SciTech Connect

    Lu, Y.; Drelich, J.; Miller, J.D.

    1998-06-15

    Oleate adsorption at an apatite surface was investigated by ex-situ Fourier transform infrared internal reflection spectroscopy (FTIR/IRS). Adsorption isotherms have been determined using an apatite internal reflection element (IRE) and it has been found that pH has a significant influence on oleate adsorption by apatite. At pH 8.0 and 20 C, oleate adsorption density increases monotonically as equilibrium oleate concentration increases from 5 {times} 10{sup {minus}6} to 1 {times} 10{sup {minus}3} M. These results are in contrast to the results at pH 9.5 and 20 C in which case the adsorption density is limited to that corresponding to approximately monolayer coverage. Oleate adsorption by apatite was compared to oleate adsorption by fluorite and calcite and the different adsorption behavior at these three mineral surfaces is attributed to the differences in the densities of surface calcium sites and to the differences in the solubilities of these minerals. Contact angles have been measured at the apatite IRE surface and it has been demonstrated that both the amount and the nature of the adsorbed species influence the hydrophobic state of the surface.

  9. Enzyme-functionalized biomimetic apatites: concept and perspectives in view of innovative medical approaches.

    PubMed

    Weber, Christina G; Mueller, Michaela; Vandecandelaere, Nicolas; Trick, Iris; Burger-Kentischer, Anke; Maucher, Tanja; Drouet, Christophe

    2014-03-01

    Biomimetic nanocrystalline calcium-deficient apatite compounds are particularly attractive for the setup of bioactive bone-repair scaffolds due to their high similarity to bone mineral in terms of chemical composition, structural and substructural features. As such, along with the increasingly appealing development of moderate temperature engineered routes for sample processing, they have widened the armamentarium of orthopedic and maxillofacial surgeons in the field of bone tissue engineering. This was made possible by exploiting the exceptional surface reactivity of biomimetic apatite nanocrystals, capable of easily exchanging ions or adsorbing (bio)molecules, thus leading to highly-versatile drug delivery systems. In this contribution we focus on the preparation of hybrid materials combining biomimetic nanocrystalline apatites and enzymes (lysozyme and subtilisin). This paper reports physico-chemical data as well as cytotoxicity evaluations towards Cal-72 osteoblast-like cells and finally antimicrobial assessments towards selected strains of interest in bone surgery. Biomimetic apatite/enzyme hybrids could be prepared in varying buffers. They were found to be non-cytotoxic toward osteoblastic cells and the enzymes retained their biological activity (e.g. bond cleavage or antibacterial properties) despite the immobilization and drying processes. Release properties were also examined. Beyond these illustrative examples, the concept of biomimetic apatites functionalized with enzymes is thus shown to be useable in practice, e.g. for antimicrobial purposes, thus widening possible therapeutic perspectives. PMID:24258399

  10. Fabrication and apatite inducing ability of different porous titania structures by PEO treatment.

    PubMed

    Rao, X; Chu, C L; Sun, Q; Zheng, Y Y

    2016-09-01

    Plasma electrolytic oxidation (PEO) was employed to grow different porous titania structures on Ti6Al4V alloy (TC4) substrate using various parameters. It was found that the PEO voltage and working frequency could affect the morphology, the pore size, the pore density, the thickness and the phase composition of titania structures. Thereafter, three typical porous titania structures with nanosize pores, microsize pores and microsize grooves were respectively selected to estimate their bioactivity using SBF immersion test. After soaking at different durations (3-28d), the surface morphology, the chemical composition as well as the phase structure of deposited apatite layers on porous titania were evaluated using SEM, EDS, and XRD. The formation of various biomimetic apatite layers indicated the different influence due to the characteristics of porous titania structures. The porous titania structure with nanosize pores could induce a fast apatite growth at the early immersion stage (~7d), while the one with microsize pores exhibited the best apatite inducing ability at long term immersion (~28d). Based on the experimental results, the formation mechanism of biomimetic apatite affected by the pore structure of titania was discussed as well. PMID:27207066

  11. In situ vitrification demonstration at Pit 1, Oak Ridge National Laboratory. Volume 1: Results of treatability study

    SciTech Connect

    Spalding, B.P.; Naney, M.T.; Cline, S.R.; Bogle, M.A.; Tixier, J.S.

    1997-12-01

    A treatability study was initiated in October 1993 to apply in situ vitrification (ISV) to at least two segments of Oak Ridge National Laboratory (ORNL) seepage Pit 1 by the end of fiscal year (FY) 1995. This treatability study was later extended to include all of Pit 1 and was performed to support a possible Interim Record of Decision or removal action for closure of one or more of the seepage pits and trenches beginning as early as FY 1997. This treatability study was carried out to establish the field-scale technical performance of ISV for (1) attaining the required depth, nominally 15 ft, to incorporate source contamination within and beneath the pits; (2) demonstrating field capability for the overlap of melt settings which will be necessary to achieve fused, melted segments of the source contamination; (3) demonstrating off-gas handling technology for accommodating and minimizing the volatilization of {sup 137}Cs; (4) demonstrating adequate site characterization techniques to predict ISV melting kinetics, processing temperatures, and product durability; and (5) promoting public acceptance of ISV technology by demonstrating its safety, implementability, site impacts, and air emissions and by coordinating the treatability study within the regulatory closure process. In April 1996 an expulsion of an estimated 10% of the 196 Mg (216 tons) melt body occurred resulting in significant damage to ISV equipment and, ultimately, led to an indefinite suspension of further ISV operations at Pit 1. This report summarizes the technical accomplishments and status of the project in fulfilling these objectives through September 1997.

  12. SUPERFUND TREATABILITY CLEARINGHOUSE: SUMMARY REPORT ON THE FIELD INVESTIGATION OF THE SAPP BATTERY SITE JACKSON COUNTY, FLORIDA

    EPA Science Inventory

    This treatability study presents the results of field investigations at the Sapp Battery site in Florida, an abandoned battery recycling operation. The site is estimated to contain 14,300 cubic yards of soils with lead levels in excess of 1,000 ppm. The soils in the immediate v...

  13. SUPERFUND TREATABILITY CLEARINGHOUSE: TECHNOLOGY DEMONSTRATION OF A THERMAL DESORPTION/UV PHOTOLYSIS PROCESS FOR DECONTAMINATING SOILS CONTAINING HERBICIDE ORANGE

    EPA Science Inventory

    This treatability study report presents the results of laboratory and field tests on the effectiveness of a new decontamination process for soils containing 2,4-D/2,4,5-T and traces of dioxin. The process employs three operations, thermal desorption, condensation and absorp...

  14. SUPERFUND TREATABILITY CLEARINGHOUSE: BDAT INCINERATION OF CERCLA SARMS AT THE JOHN ZINK COMPANY TEST FACILITY (FINAL PROJECT REPORT)

    EPA Science Inventory

    This report presents the results of a treatability study of rotary kiln incineration of a synthetic "Superfund soil" bearing a wide range of chemical contaminants typically occurring at Superfund sites. This surrogate soil is referred to as a synthetic analytical reference ...

  15. EVALUATION OF CONTAMINANT LEACHABILITY FACTORS BY COMPARISON OF TREATABILITY STUDY DATA FOR MULTIPLE SOLIDIFIED/STABILIZED MATERIALS

    EPA Science Inventory

    Solidification/stabilization (S/S) technology is widely used in the treatment of hazardous waste and contaminated soil in the US. In a project sponsored by the US Navy and the USEPA, treatability test data were compiled into a data base listing contaminant concentration and matri...

  16. Treatability Test Report: Characterization of Vadose Zone Carbon Tetrachloride Source Strength Using Tomographic Methods at the 216-Z-9 Site

    SciTech Connect

    Truex, Michael J.; Carroll, Kenneth C.; Rohay, Virginia J.; Mackley, Rob D.; Parker, Kyle R.

    2012-09-28

    A treatability test was conducted in 2011 at the 216-Z-9 Trench to evaluate methods for collecting characterization information that supports refined assessment of SVE performance goals based on impact to groundwater. The characterization information can also provide input to operational strategies for continued SVE operation and decisions regarding closure of the SVE system or transition to other remedies, if necessary.

  17. Apatite (U-Th)/He thermochronology dataset interpretation: New insights from physical point of view

    NASA Astrophysics Data System (ADS)

    Gautheron, Cécile; Mbongo-Djimbi, Duval; Gerin, Chloé; Roques, Jérôme; Bachelet, Cyril; Oliviero, Erwan; Tassan-Got, Laurent

    2015-04-01

    The apatite (U-Th)/He (AHe) system has rapidly become a very popular thermochronometer to constrain burial and exhumation phases in a variety of geological contexts. However, the interpretation of AHe data depends on a precise knowledge of He diffusion in apatite. Several studies suggest that radiation damage generated by U and Th decay can create traps for He atoms, increasing He retention for irradiated minerals. The radiation damage also anneals with temperature and the amount of damage in an apatite crystal is at any time a balance between production and annealing, controlled by U-Th concentration, grain chemistry and thermal history (Flowers et al., 2009; Gautheron et al., 2009; 2013). However the models are not well constrained and do not fully explain the mechanism of He retention. In order to have a deeper insight on this issue, multidisciplinary studies on apatite combining diffusion experiments by Elastic Recoil Diffusion Analysis (ERDA) with a multi-scale theoretical diffusion calculation based on Density Functional Theory (DFT) and Kinetic Monte Carlo were performed. ERDA experiments were conducted on different macro-crystals, and we probed the shape of a He profile implanted into a planar and polished surface of the crystal. The helium profile evolves with temperature and allows quantifying the He diffusivity and damage impact. Additionally, DFT calculations of a damage-free crystal of apatite with different F and Cl compositions, in similar proportion as natural ones, have been run to find the favored paths of a helium atom between interstitial sites, leading to a computation of the activation energy and the diffusion coefficient. We show that damage free apatite crystals are characterized by low retention behavior and closure temperature range from 33-36°C for pure F-apatite to higher value for Cl riche apatite (up to 12°C higher), for typical grain size and cooling rate (Mbongo-Djimbi et al., in review). Using ERDA and DFT approaches, we

  18. Enamel-like apatite crown covering amorphous mineral in a crayfish mandible.

    PubMed

    Bentov, Shmuel; Zaslansky, Paul; Al-Sawalmih, Ali; Masic, Admir; Fratzl, Peter; Sagi, Amir; Berman, Amir; Aichmayer, Barbara

    2012-01-01

    Carbonated hydroxyapatite is the mineral found in vertebrate bones and teeth, whereas invertebrates utilize calcium carbonate in their mineralized organs. In particular, stable amorphous calcium carbonate is found in many crustaceans. Here we report on an unusual, crystalline enamel-like apatite layer found in the mandibles of the arthropod Cherax quadricarinatus (freshwater crayfish). Despite their very different thermodynamic stabilities, amorphous calcium carbonate, amorphous calcium phosphate, calcite and fluorapatite coexist in well-defined functional layers in close proximity within the mandible. The softer amorphous minerals are found primarily in the bulk of the mandible whereas apatite, the harder and less soluble mineral, forms a wear-resistant, enamel-like coating of the molar tooth. Our findings suggest a unique case of convergent evolution, where similar functional challenges of mastication led to independent developments of structurally and mechanically similar, apatite-based layers in the teeth of genetically remote phyla: vertebrates and crustaceans. PMID:22588301

  19. Enamel-like apatite crown covering amorphous mineral in a crayfish mandible

    PubMed Central

    Bentov, Shmuel; Zaslansky, Paul; Al-Sawalmih, Ali; Masic, Admir; Fratzl, Peter; Sagi, Amir; Berman, Amir; Aichmayer, Barbara

    2012-01-01

    Carbonated hydroxyapatite is the mineral found in vertebrate bones and teeth, whereas invertebrates utilize calcium carbonate in their mineralized organs. In particular, stable amorphous calcium carbonate is found in many crustaceans. Here we report on an unusual, crystalline enamel-like apatite layer found in the mandibles of the arthropod Cherax quadricarinatus (freshwater crayfish). Despite their very different thermodynamic stabilities, amorphous calcium carbonate, amorphous calcium phosphate, calcite and fluorapatite coexist in well-defined functional layers in close proximity within the mandible. The softer amorphous minerals are found primarily in the bulk of the mandible whereas apatite, the harder and less soluble mineral, forms a wear-resistant, enamel-like coating of the molar tooth. Our findings suggest a unique case of convergent evolution, where similar functional challenges of mastication led to independent developments of structurally and mechanically similar, apatite-based layers in the teeth of genetically remote phyla: vertebrates and crustaceans. PMID:22588301

  20. Échange terres rares légères Ca dans l'apatite

    NASA Astrophysics Data System (ADS)

    Iqdari, Abderrahmane; Velde, Bruce; Benalioulhaj, Noureddine; Dujon, Saint-Clair; El Yamine, Nacer

    2003-04-01

    Diffusion experiments were carried out on natural apatite crystals that were immersed in molten light rare earth element (REE) chloride salt at temperatures between 900 and 1150 °C for periods up to 35 days. Electron microprobe analysis of the crystals showed that light REEs replaced Ca according to electronic balance, i.e. 2 REE3+ for 3 Ca2+. These diffusion profiles indicate that a maximum amount of substitution in the structure occurs when two of the ten Ca ions in apatite are replaced by the REE diffusing elements. Anisotropic diffusion is observed between a and c crystallographic directions. Comparison of maximum distance indicates that the larger ions move more easily in the apatite structure. We conclude that the light REEs diffuse within the channel structures of the mineral, and that this diffusion is controlled by the substitution type of elements in the calcium sites. To cite this article: A. Iqdari et al., C. R. Geoscience 335 (2003).

  1. Characterization of a calcium phospho-silicated apatite with iron oxide inclusions

    NASA Astrophysics Data System (ADS)

    Desport, Barthélémy; Carpena, Joëlle; Lacout, Jean-Louis; Borschneck, Daniel; Gattacceca, Jérôme

    2011-02-01

    An iron oxide containing calcium phosphate-silicate hydroxyapatite was synthesized by calcination at 900 °C of a sample obtained by precipitation in basic aqueous solution of Ca, P, Si, Fe and Mg containing acidic solution made from dissolution of natural minerals. XRD and FTIR were used for crystallographic characterization of the main apatitic phase. Its composition was determined using ICP-AES. EDX coupled with SEM and TEM evidenced the heterogeneity of this compound and the existence of iron-magnesium oxide. Magnetic analyses highlighted that this phase was non-stoichiometric magnesioferrite (Mg 1.2Fe 1.8O 3.9) spherical nanoparticles. Those analyses also put into evidence the role of calcination in synthesis. Carbonates detected by FTIR and estimated by SEM-EDX in non-calcinated sample were removed from apatitic structure, and crystallization of apatite was enhanced during heating. Moreover, there was phase segregation that led to magnesioferrite formation.

  2. Revised phosphate-water fractionation equation reassessing paleotemperatures derived from biogenic apatite

    NASA Astrophysics Data System (ADS)

    Pucéat, E.; Joachimski, M. M.; Bouilloux, A.; Monna, F.; Bonin, A.; Motreuil, S.; Morinière, P.; Hénard, S.; Mourin, J.; Dera, G.; Quesne, D.

    2010-09-01

    Oxygen isotopes of biogenic apatite have been widely used to reassess anomalous temperatures inferred from oxygen isotope ratios of ancient biogenic calcite, more prone to diagenetic alteration. However, recent studies have highlighted that oxygen isotope ratios of biogenic apatite differ dependent on used analytical techniques. This questions the applicability of the phosphate-water fractionation equations established over 25 years ago using earlier analytical techniques to more recently acquired data. In this work we present a new phosphate-water oxygen isotope fractionation equation based on oxygen isotopes determined on fish raised in aquariums at controlled temperature and with monitored water oxygen isotope composition. The new equation reveals a similar slope, but an offset of about + 2‰ to the earlier published equations. This work has major implications for paleoclimatic reconstructions using oxygen isotopes of biogenic apatite since calculated temperatures have been underestimated by about 4 to 8 °C depending on applied techniques and standardization of the analyses.

  3. Preliminary Apatite Fission Track Thermochronology of Wrangel Island, Arctic Russia

    NASA Astrophysics Data System (ADS)

    Dumitru, T. A.; Miller, E. L.

    2010-12-01

    Wrangel Island is part of a regional structural high that forms the continuation of the offshore Herald Arch and Chukchi Platform of Alaska. It is flanked on the north by the deep North Chukchi Basin, which in addition to Paleozoic strata, is inferred to contain up to 12 km of Beaufortian and Brookian (Late Jurassic to Tertiary) sediments (Dinkelman et al., 2008). To the south, ~E-W trending faults bound the Longa Basin that separates Wrangel from mainland Chukotka. This basin lies along strike of the early Tertiary Hope Basin in the Alaskan offshore. Wrangel Island itself exposes a broad, doubly-plunging anticlinorium-like structure cored by Neoproterozoic basement and flanked by Paleozoic shelf successions and a thick section of Triassic turbidites, representing about 5-7 km of structural section. The structural geology of Wrangel Island has been interpreted to represent a north-vergent Mesozoic fold and thrust belt linked by seismic reflection to the Herald Arch and then to the Lisburne Hills and the Brooks Range foreland fold and thrust belt (e.g. Kos’ko et al., 1993). However, deformation differs considerably from typical foreland fold-thrust structures of the Brooks Range as it is penetrative, involves large strains, and occurred under greenschist facies metamorphic conditions. Parts of the sequence exhibit mylonitic fabrics. Apatite fission track thermochronology of rocks from Wrangel Island can establishes the age of cooling to temperatures below ~ 100° C, providing temporal constraints on the uplift and erosional history of rocks that form this regional structural high. We analyzed seven fission track samples from a 9-km long N-S transect along the Kishchnikov River, from Triassic strata on the southern flank of the anticlinal structure to Devonian(?)-Mississippian feldspathic grits, conglomerates, and underlying Neoproterozoic igneous basement rocks in its core. All samples yielded statistically indistinguishable fission track ages averaging about 95

  4. TREATABILITY STUDIES USED TO TEST FOR EXOTHERMIC REACTIONS OF PLUTONIUM DECONTAMINATION CHEMICALS

    SciTech Connect

    EWALT, J.R.

    2005-06-06

    Fluor Hanford is decommissioning the Plutonium Finishing Plant (PFP) at the Hanford site in Eastern Washington. Aggressive chemicals are commonly used to remove transuranic contaminants from process equipment to allow disposal as low level waste. Chemicals being considered for decontamination of gloveboxes in PFP include cerium(IV) nitrate in a nitric acid solution, and proprietary commercial solutions that include acids, degreasers, and sequestering agents. Fluor's decontamination procedure involves application of chemical solutions as a spray on the contaminated surfaces, followed by a wipe-down with rags. This process effectively transfers the transuranic materials to the decontamination liquids, which are then absorbed by rags and packaged for disposal as TRU waste. Concerns regarding the safety of this procedure developed following a fire at Rocky Flats in 2003. The fire occurred in a glovebox that had been treated with cerium nitrate, which is one of the decontamination chemicals that Fluor Hanford has proposed to use. The investigation of the event was hampered by the copious use of chemicals and water to extinguish the fire, and was not conclusive regarding the cause. However, the reviewers noted that rags were found in the glovebox, suggesting that the combination of rags and chemicals may have contributed to the fire. With that uncertainty, Fluor began an investigation into the potential for fire when using the chemicals and materials in the decontamination process. The focus of this work has been to develop a disposal strategy that will provide a chemically stable waste form at expected Hanford waste storage temperatures. Treatability tests under CERCLA were used to assess the use of certain chemicals and wipes during the decontamination process. Chemicals being considered for decontamination of gloveboxes at PFP include cerium (IV) nitrate in a nitric acid solution, and proprietary commercial solutions as RadPro{trademark} that include acids, degreasers

  5. Differential fluorescence EEMs can be used to assess treatability of DOM during drinking water production

    NASA Astrophysics Data System (ADS)

    Lavonen, Elin; Kothawala, Dolly; Tranvik, Lars; Köhler, Stephan

    2014-05-01

    Fluorescence spectroscopy has been widely used to characterize fluorescent dissolved organic matter (FDOM) in various waters including during drinking water production. Commonly used techniques for data treatment include peak picking, indexes calculated from 2D emission spectra and modelling of fluorescence components using parallel factor analysis (PARAFAC). However, peak picking and indexes only use limited information from the fluorescence EEMs and PARAFAC requires a larger dataset and experience to perform. Because DOM is a major issue in drinking water production, and personnel at water treatment plants usually have limited time for advanced analysis we have developed a simple way of assessing the treatability of DOM in different waters using differential fluorescence. With this approach the removed fraction of FDOM is calculated from samples taken before and after a particular treatment process and the percentage of removed material assessed. Samples have been collected from four large water treatment plants in Sweden and analyzed for 3Dfluorescence, absorbance and DOC. The selective removal of DOM during e.g. flocculation and slow sand filtration as well as differences in experienced treatability between the treatment plants was described with differential fluorescence. Chemical flocculation is selective towards FDOM with red-shifted emission across the entire EEM. Red-shift has earlier been connected to condensation (i.e. decrease in H/C) and positively correlated to molecular size indicating that larger, humified molecules are being preferentially removed. During the biological process of slow sand filtration compounds with blue-shifted emission are targeted demonstrating selective removal of more freshly produced, microbial material. Disinfection with UV/NH2Cl and NaOCl was found to only target material with protein-like fluorescence suggesting that FDOM of this nature could be responsible for unwanted consumption of disinfection agent. Targeted removal

  6. Green apatites: hydride ions, electrons and their interconversion in the crystallographic channel.

    PubMed

    Hayashi, Katsuro; Hosono, Hideo

    2016-03-01

    Hydride (H(-)) ions and electrons in channel sites of the lattice of calcium phosphate apatites are characterized. Solid-state chemical reduction using TiH2 is effective for doping of H(-) ions into apatites. Irradiation of the H(-) ion-doped apatite with ultraviolet (UV) light induces green coloration. Electron paramagnetic resonance (EPR) reveals that this colour centre is attributed to electrons captured at a vacant anion site in the crystallographic channel, forming F(+) centres. Transient H(0) atoms are detected at low temperatures by EPR. The concentration of UV-induced electrons in the apatite at room temperature decays according to second-order kinetics because of the chemical reactions involving two electrons; overall, electron generation and thermal decay can be described as: H(-) + O(2-) ↔ 2e(-) + OH(-). (1)H magic angle spinning nuclear magnetic resonance spectroscopy is used to identify H(-) ions in the apatite, which are characterized by a chemical shift of +3.4 ppm. Various types of O-H groups including OH(-) ions in the channel and protons bound to phosphate groups are concurrently formed, and are identified by considering the relationship between the O-H stretching frequency and the (1)H chemical shift. The complementary results obtained by EPR and NMR reveal that the H(-) ions and transient H(0) atoms are located at the centre of Ca3 triangles in the apatite, while the electrons are located in the centre of Ca6 octahedra. These findings provide an effective approach for identifying new classes of mixed-oxide-hydride or -electride crystals. PMID:26928237

  7. Adsorption of nucleotides on biomimetic apatite: The case of adenosine 5‧ triphosphate (ATP)

    NASA Astrophysics Data System (ADS)

    Hammami, Khaled; El-Feki, Hafed; Marsan, Olivier; Drouet, Christophe

    2016-01-01

    ATP is a well-known energy supplier in cells. The idea to associate ATP to pharmaceutical formulations/biotechnological devices to promote cells activity by potentially modulating their microenvironment thus appears as an appealing novel approach. Since biomimetic nanocrystalline apatites have shown great promise for biomedical applications (bone regeneration, cells diagnostics/therapeutics, …), thanks to a high surface reactivity and an intrinsically high biocompatibility, the present contribution was aimed at exploring ATP/apatite interactions. ATP adsorption on a synthetic carbonated nanocrystalline apatite preliminarily characterized (by XRD, FTIR, Raman, TG-DTA and SEM-EDX) was investigated in detail, pointing out a good agreement with Sips isothermal features. Adsorption characteristics were compared to those previously obtained on monophosphate nucleotides (AMP, CMP), unveiling some specificities. ATP was found to adsorb effectively onto biomimetic apatite: despite smaller values of the affinity constant KS and the exponential factor m, larger adsorbed amounts were reached for ATP as compared to AMP for any given concentration in solution. m < 1 suggests that the ATP/apatite adsorption process is mostly guided by direct surface bonding rather than through stabilizing intermolecular interactions. Although standard ΔGads ° was estimated to only -4 kJ/mol, the large value of Nmax led to significantly negative effective ΔGads values down to -33 kJ/mol, reflecting the spontaneous character of adsorption process. Vibrational spectroscopy data (FTIR and Raman) pointed out spectral modifications upon adsorption, confirming chemical-like interactions where both the triphosphate group of ATP and its nucleic base were involved. The present study is intended to serve as a basis for future research works involving ATP and apatite nanocrystals/nanoparticles in view of biomedical applications (e.g. bone tissue engineering, intracellular drug delivery, …).

  8. Adsorption of nucleotides on biomimetic apatite: The case of cytidine 5' monophosphate (CMP).

    PubMed

    Choimet, Maëla; Tourrette, Audrey; Drouet, Christophe

    2015-10-15

    The chemical interaction between DNA macromolecules and hard tissues in vertebrate is of foremost importance in paleogenetics, as bones and teeth represent a major substrate for the genetic material after cell death. Recently, the empirical hypothesis of DNA "protection" over time thanks to its adsorption on hard tissues was revisited from a physico-chemical viewpoint. In particular, the existence of a strong interaction between phosphate groups of DNA backbone and the surface of apatite nanocrystals (mimicking bone/dentin mineral) was evidenced on an experimental basis. In the field of nanomedicine, DNA or RNA can be used for gene transport into cells, and apatite nanocarriers then appear promising. In order to shed some more light on interactions between DNA molecules and apatite, the present study focuses on the adsorption of a "model" nucleotide, cytidine 5' monophosphate (CMP), on a carbonated biomimetic apatite sample. The follow-up of CMP kinetics of adsorption pointed out the rapidity of interaction with stabilization reached within few minutes. The adsorption isotherm could be realistically fitted to the Sips model (Langmuir-Freundlich) suggesting the influence of surface heterogeneities and adsorption cooperativity in the adsorption process. The desorption study pointed out the reversible character of CMP adsorption on biomimetic apatite. This contribution is intended to prove helpful in view of better apprehending the molecular interaction of DNA fragments and apatite compounds, independently of the application domain, such as bone diagenesis or nanomedicine. This study may also appear informative for researchers interested in the origins of life on Earth and the occurrence and behavior of primitive biomolecules. PMID:26117294

  9. Theoretical stability assessment of uranyl phosphates and apatites: selection of amendments for in situ remediation of uranium.

    PubMed

    Raicevic, S; Wright, J V; Veljkovic, V; Conca, J L

    2006-02-15

    Addition of an amendment or reagent to soil/sediment is a technique that can decrease mobility and reduce bioavailability of uranium (U) and other heavy metals in the contaminated site. According to data from literature and results obtained in field studies, the general mineral class of apatites was selected as a most promising amendment for in situ immobilization/remediation of U. In this work we presented theoretical assessment of stability of U(VI) in four apatite systems (hydroxyapatite (HAP), North Carolina Apatite (NCA), Lisina Apatite (LA), and Apatite II) in order to determine an optimal apatite soil amendment which could be used for in situ remediation of uranium. In this analysis we used a theoretical criterion which is based on calculation of the ion-ion interaction potential, representing the main term of the cohesive energy of the matrix/pollutant system. The presented results of this analysis indicate (i) that the mechanism of immobilization of U by natural apatites depends on their chemical composition and (ii) that all analyzed apatites represent, from the point of view of stability, promising materials which could be used in field remediation of U-contaminated sites. PMID:15885755

  10. Mineralogy and geochemistry of Fe-Ti oxide and apatite (nelsonite) deposits and evaluation of the liquid immiscibility hypothesis.

    USGS Publications Warehouse

    Kolker, A.

    1982-01-01

    The modal mineralogy for 32 Fe-Ti oxides and apatites supports the 2:1 oxide:apatite ratio for these samples from New York, Quebec, Norway and Sweden. Accessory minerals include: biotite, clinoamphibole, spinel, zircon and sulphides, oxygen fugacities range from 10-11 to 10-20, and T 600o to 1000oC. - K.A.R.

  11. Insights into the behaviour of S, F, and Cl at Santiaguito Volcano, Guatemala, from apatite and glass

    NASA Astrophysics Data System (ADS)

    Scott, Jeannie A. J.; Humphreys, Madeleine C. S.; Mather, Tamsin A.; Pyle, David M.; Stock, Michael J.

    2015-09-01

    The mineral apatite can incorporate all of the major magmatic volatile species into its structure. Where melt inclusions are not available, magmatic apatite may therefore represent an opportunity to quantify volatile concentrations in the pre-eruptive melt. We analysed apatites and matrix glasses from andesites and dacites erupted from Santiaguito Volcano, Guatemala, between the 1920s and 2002. X-ray mapping shows complex zoning of sulphur in the apatite grains, but typically with sulphur-rich cores and sulphur-poor rims. Apatite microphenocrysts are enriched in F and depleted in Cl relative to inclusions. Matrix glasses are dacite to rhyolite and contain low F but up to 2400 ppm Cl. Overall, the data are consistent with progressive depletion of Cl in the most evolved melts due to crystallisation and degassing. In the absence of pristine melt inclusions, we used apatite, together with published partitioning data, to reconstruct the likely volatile contents of the pre-eruptive melt, and hence estimate long-term average gas emissions of SO2, HF and HCl for the ongoing eruption. The data indicate time-averaged SO2 emissions of up to 157 tonnes/day, HCl of 74-1382 tonnes/day and up to 196 tonnes/day HF. Apatite may provide a useful measure of long-term volatile emissions at volcanoes where direct emissions measurements are unavailable, or for comparison with intermittent gas sampling methods. However, significant uncertainty remains regarding volatile distribution coefficients for apatite, and their variations with temperature and pressure.

  12. In vitro apatite formation on organic polymers modified with a silane coupling reagent

    PubMed Central

    Shirosaki, Yuki; Kubo, Masaaki; Takashima, Seisuke; Tsuru, Kanji; Hayakawa, Satoshi; Osaka, Akiyoshi

    2005-01-01

    γ-Methacryloxypropyltrimethoxysilane (γ-MPS) was grafted to high-density polyethylene, polyamide and silicone rubber substrates by the emulsion polymerization procedure in order to provide these organic polymers with in vitro apatite-forming ability. The contact angles towards distilled water of the γ-MPS-grafted specimens were lower than those of the original organic polymer specimens, indicating that the grafted substrates were more hydrophilic. The in vitro apatite formation in a simulated body fluid (Kokubo solution) was confirmed for several of the γ-MPS-grafted specimens. PMID:16849191

  13. Growth of apatite on chitosan-multiwall carbon nanotube composite membranes

    NASA Astrophysics Data System (ADS)

    Yang, Jun; Yao, Zhiwen; Tang, Changyu; Darvell, B. W.; Zhang, Hualin; Pan, Lingzhan; Liu, Jingsong; Chen, Zhiqing

    2009-07-01

    Bioactive membranes for guided tissue regeneration would be of value for periodontal therapy. Chitosan-multiwall carbon nanotube (CS-MWNT) composites were treated to deposit nanoscopic apatite for MWNT proportions of 0-4 mass%. Fourier-transform infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray analysis, and X-ray diffraction were used for characterization. Apatite was formed on the CS-MWNT composites at low MWNT concentrations, but the dispersion of the MWNT affects the crystallite size and the Ca/P molar ratio of the composite. The smallest crystallite size was 9 nm at 1 mass% MWNT.

  14. Apatite: A New Tool For Understanding The Temporal Variability Of Magmatic Volatile Contents

    NASA Astrophysics Data System (ADS)

    Stock, M. J.; Humphreys, M.; Smith, V.; Pyle, D. M.; Isaia, R.

    2015-12-01

    The apatite crystal structure is capable of incorporating H2O, F and Cl, as well as trace CO2 and sulphur. These can be related to parental magma compositions through application of a series of pressure and temperature-dependent exchange reactions (Piccoli and Candela, 1994), permitting apatite crystals to preserve a record of all major volatile species in the melt. Furthermore, due to the general incompatibility of P in other rock-forming minerals, apatite is ubiquitous in igneous systems and often begins crystallising early, such that apatite inclusions within phenocrysts record melt volatile contents throughout magmatic differentiation. In this work, we compare the compositions of apatite inclusions and microphenocrysts with pyroxene-hosted melt inclusions from the Astroni 1 eruption of Campi Flegrei, Italy. These data are coupled with magmatic differentiation models (Gualda et al., 2012), experimental volatile solubility data (Webster et al., 2014) and thermodynamic models of apatite compositional variations (Piccoli and Candela, 1994) to determine a time-series of magmatic volatile evolution in the build-up to eruption. We find that apatite halogen/OH ratios decreased through magmatic differentiation, while melt inclusion F and Cl concentrations increased. Melt inclusion H2O contents are constant at ~2.5 wt%. These data are best explained by volatile-undersaturated differentiation over most of the crystallisation history of the Astroni 1 melt, with melt inclusion H2O contents reset during ascent, due to rapid H diffusion through the phenocryst hosts (Woods et al., 2000). Given the rapid diffusivity of volatiles in apatite (Brenan, 1993), preservation of undersaturated compositions in microphenocrysts suggests that saturation was only achieved a few days to months before eruption and that it may have been the transition into a volatile-saturated state that ultimately triggered eruption. Piccoli and Candela, 1994. Am. J. of Sc., 294, 92-135. Gualda et al., 2012

  15. Bench- and pilot-scale thermal desorption treatability studies on pesticide-contaminated soils from Rocky Mountain Arsenal

    SciTech Connect

    Swanstrom, C.P.; Besmer, M.

    1995-03-09

    Thermal desorption is being considered as a potential remediation technology for pesticide-contaminated soils at the Rocky Mountain Arsenal (RMA) in Denver, Colorado. From 1988 through 1992, numerous laboratory- and bench-scale indirect-heated thermal desorption (IHTD) treatability studies have been performed on various soil medium groups from the arsenal. RMA has contracted Argonne National Laboratory to conduct a pilot-scale direct-fired thermal desorption (DFTD) treatability study on pesticide-contaminated RMA soil. The purpose of this treatability study is to evaluate the overall effectiveness of the DFTD technology on contaminated RMA soils and to provide data upon which future conceptual design assumptions and cost estimates for a full-scale system can be made. The equipment used in the DFTD treatability study is of large enough scale to provide good full-scale design parameters and operating conditions. The study will also provide valuable-emissions and materials-handling data. Specifically this program will determine if DFTD can achieve reductions in soil contamination below the RMA preliminary remediation goals (PRGs), define system operating conditions for achieving the PRGs, and determine the fate of arsenic and other hazardous metals at these operating conditions. This paper intends to compare existing data from a bench-scale IHTD treatability study using equipment operated in the batch mode to new data from a pilot-scale DFTD operated in a parallel-flow continuous mode. Delays due to materials-handling problems and permit issues have delayed the start of the pilot-scale DFTD testing. The first pilot-scale test is scheduled for the flat week in January 1995. The available data will be presented March 9, 1995, at the Seventh Annual Gulf Coast Environmental Conference in Houston, Texas.

  16. Biodegradability oriented treatability studies on high strength segregated wastewater of a woolen textile dyeing plant.

    PubMed

    Baban, Ahmet; Yediler, Ayfer; Ciliz, NilgunKiran; Kettrup, Antonius

    2004-11-01

    Textile dyeing and finishing industry involves considerable amount of water usage as well as polluted and highly colored wastewater discharges. Biological treatability by means of mineralization, nitrification and denitrification of high strength woolen textile dye bathes, first- and second-rinses is presented. COD fractionation study was carried out and kinetic parameters were determined. Biodegradability of organic compounds in highly loaded composite wastewater after segregation and the effluent of applied biological treatment of high strength composite wastewater were measured by determining oxygen consumption rates. The results were used in terms of assessing an alternative method for inert COD fractionation. The study implied that about 80% soluble COD, 50% color and 75% toxicity reduction were possible by single sludge biological processes. Sixteen per cent of total COD was found to be initially inert. Inert fraction was increased to 22% by production of soluble and particulate microbial products through biological treatment. PMID:15488936

  17. Two Unusual but Treatable Causes of Refractory Ascites After Liver Transplantation.

    PubMed

    Novelli, P M; Shields, J; Krishnamurthy, V; Cho, K

    2015-12-01

    Refractory ascites (RA) is thought to complicate the postoperative course of 5-7% (Nishida et al. in Am J Transplant. 6: 140-149, 2006; Gotthardt et al. in Ann Transplant. 18: 378-383, 2013) of liver transplant recipients. RA after liver transplantation is often a frustrating diagnostic dilemma with few good management options unless an obvious mechanical factor is identified. Supportive therapies often fail until a treatable precipitating cause is identified and removed. We describe two patients who developed RA following liver transplantation for primary sclerosing cholangitis, and hepatitis C and alcoholic liver disease, respectively. The cause for RA was hyperkinetic portal hypertension secondary to splenomegaly in the first case and a pancreatic AVM in the 2nd case. After failure of other interventions, surgical splenectomy resulted in immediate and durable resolution of the previously intractable ascites. PMID:26017456

  18. Gunite and Associated Tanks Treatability Study Equipment Testing at the Tanks Technology Cold Test Facility

    SciTech Connect

    Burks, BL

    2001-02-27

    This report provides a summary of the cold tests performed on the equipment to be used in the Gunite and Associated Tanks Treatability Study. The testing was performed from June 1996 to May 1997 at the Tanks Technology Cold Test Facility located at the 7600 complex at Oak Ridge National Laboratory. Testing of specific equipment grouped into the following sections: (1) Modified Light-Duty Utility Arm Testing, (2) Remotely Operated Vehicle Testing, (3) Waste Dislodging and Conveyance System and Balance of Plant Equipment Testing, (4) Camera and Lighting System Testing, and (5) Characterization End-Effector Testing. Each section contains descriptions of a series of tests that summarize the test objectives, testing performed, and test results. General conclusions from the testing are also provided.

  19. AMPD2 Regulates GTP Synthesis and is Mutated in a Potentially-Treatable Neurodegenerative Brainstem Disorder

    PubMed Central

    Akizu, Naiara; Cantagrel, Vincent; Schroth, Jana; Cai, Na; Vaux, Keith; McCloskey, Douglas; Naviaux, Robert K.; Vleet, Jeremy Van; Fenstermaker, Ali G.; Silhavy, Jennifer L.; Scheliga, Judith S.; Toyama, Keiko; Morisaki, Hiroko; Sonmez, Fatma Mujgan; Celep, Figen; Oraby, Azza; Zaki, Maha S.; Al-Baradie, Raidah; Faqeih, Eissa; Saleh, Mohammad; Spencer, Emily; Rosti, Rasim Ozgur; Scott, Eric; Nickerson, Elizabeth; Gabriel, Stacey; Morisaki, Takayuki; Holmes, Edward W.; Gleeson, Joseph G.

    2013-01-01

    Purine biosynthesis and metabolism, conserved in all living organisms, is essential for cellular energy homeostasis and nucleic acids synthesis. The de novo synthesis of purine precursors is under tight negative feedback regulation mediated by adenosine and guanine nucleotides. We describe a new distinct early-onset neurodegenerative condition resulting from mutations in the adenosine monophosphate deaminase 2 gene (AMPD2). Patients have characteristic brain imaging features of pontocerebellar hypoplasia (PCH), due to loss of brainstem and cerebellar parenchyma. We found that AMPD2 plays an evolutionary conserved role in the maintenance of cellular guanine nucleotide pools by regulating the feedback inhibition of adenosine derivatives on de novo purine synthesis. AMPD2 deficiency results in defective GTP-dependent initiation of protein translation, which can be rescued by administration of purine precursors. These data suggest AMPD2-related PCH as a new, potentially treatable early-onset neurodegenerative disease. PMID:23911318

  20. Treatability study for removal of leachable mercury in crushed fluorescent lamps

    SciTech Connect

    Bostick, W.D.; Beck, D.E.; Bowser, K.T.

    1996-02-01

    Nonserviceable fluorescent lamps removed from radiological control areas at the Oak Ridge Department of Energy facilities have been crushed and are currently managed as mixed waste (hazardous and radiologically contaminated). We present proposed treatment flowsheets and supporting treatability study data for conditioning this solid waste residue so that it can qualify for disposal in a sanitary landfill. Mercury in spent fluorescent lamps occurs primarily as condensate on high-surface-area phosphor material. It can be solubilized with excess oxidants (e.g., hypochlorite solution) and stabilized by complexation with halide ions. Soluble mercury in dechlorinated saline solution is effectively removed by cementation with zero-valent iron in the form of steel wool. In packed column dynamic flow testing, soluble mercury was reduced to mercury metal and insoluble calomel, loading > 1.2 g of mercury per grain of steel wool before an appreciable breakthrough of soluble mercury in the effluent.

  1. A treatable metabolic cause of encephalopathy: cobalamin C deficiency in an 8-year-old male.

    PubMed

    Krueger, Jena M; Piantino, Juan; Smith, Craig M; Angle, Brad; Venkatesan, Charu; Wainwright, Mark S

    2015-01-01

    Neurologic regression in a previously healthy child may be caused by metabolic or neurodegenerative disorders, many of which have no definitive treatment. We report a case of a previously healthy 8-year-old boy who presented with a month-long history of waxing and waning encephalopathy and acute regression, followed by seizures. Evaluation for a metabolic disorder revealed methylmalonic acidemia and hyperhomocysteinemia of the cobalamin C type due to a single, presumed homozygous pathogenic c.394 C>T mutation in the MMACHC gene. With the appropriate diet restrictions and vitamin replacement, he improved significantly and returned to his premorbid level of behavior. This case illustrates an unusual presentation of a treatable metabolic disorder and highlights the need to consider cobalamin defects in the differential diagnosis of healthy children with neurologic regression. PMID:25511120

  2. Deep Vadose Zone Treatability Test for the Hanford Central Plateau: Interim Post-Desiccation Monitoring Results

    SciTech Connect

    Truex, Michael J.; Oostrom, Martinus; Strickland, Christopher E.; Johnson, Timothy C.; Johnson, Christian D.; Clayton, Ray E.; Chronister, Glen B.

    2013-09-01

    A field test of desiccation is being conducted as an element of the deep vadose zone treatability test program. Desiccation technology relies on removal of water from a portion of the subsurface such that the resultant low moisture conditions inhibit downward movement of water and dissolved contaminants. Previously, a field test report (Truex et al. 2012a) was prepared describing the active desiccation portion of the test and initial post-desiccation monitoring data. Additional monitoring data have been collected at the field test site during the post-desiccation period and is reported herein along with interpretation with respect to desiccation performance. This is an interim report including about 2 years of post-desiccation monitoring data.

  3. 3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures.

    PubMed

    Coşkun, Turgay; Aydin, Halil Ibrahim; Kiliç, Mustafa; Dursun, Ali; Haliloğlu, Göknur; Topaloğlu, Haluk; Karli-Oğuz, Kader; de Koning, Tom J

    2009-01-01

    Serine deficiency disorders are a new group of neurometabolic diseases resulting from a deficiency in one of the three enzymes in the biosynthetic pathway of L-serine. Deficiency of the enzyme 3-phosphoglycerate dehydrogenase (3-PGDH), which catalyzes the first step in the biosynthetic pathway, leads to congenital microcephaly, severe psychomotor retardation, and intractable seizures. We report a 4 1/2-year-old boy who presented with congenital microcephaly, psychomotor retardation, hypertonia, strabismus, and drug-resistant seizures due to 3-PGDH deficiency. His seizures responded to L-serine and glycine supplementation only. This potentially treatable disease should be borne in mind in patients with congenital microcephaly, psychomotor retardation and seizures. A timely diagnosis based on the detection of low cerebrospinal fluid levels of L-serine and glycine is expected to further increase the success of L-serine and glycine supplementation in these patients. PMID:20196394

  4. Normal-pressure hydrocephalus and the saga of the treatable dementias

    SciTech Connect

    Friedland, R.P. )

    1989-11-10

    A case study of a 74-year-old woman is presented which illustrates the difficulty of understanding dementing illnesses. A diagnosis of normal-pressure hydrocephalus (NPH) was made because of the development of abnormal gait, with urinary incontinence and severe, diffuse, white matter lesions on the MRI scan. Computed tomographic, MRI scans and positron emission tomographic images of glucose use are presented. The treatable dementias are a large, multifaceted group of illnesses, of which NPH is one. The author proposes a new term for this disorder commonly known as NPH because the problem with the term normal-pressure hydrocephalus is that the cerebrospinal fluid pressure is not always normal in the disease.

  5. Treatability Testing of an In Situ Biostimulation Barrier for Nitrate and Chromium Treatment - 9126

    SciTech Connect

    Truex, Michael J.; Vermeul, Vincent R.; Fruchter, Jonathan S.

    2008-11-14

    An ongoing treatability test is evaluating in situ biostimulation at the 100-D Area of the Hanford Site in Richland, Washington. This test is part of a strategy to couple multiple technologies to accelerate cleanup of hexavalent-chromium contaminated groundwater discharging into the Columbia River. A permeable chemical reducing barrier was previously applied as the primary treatment to prevent the chromium plume from reaching the river at concentrations that exceed regulatory standards. In situ biostimulation is intended to provide supplemental treatment upgradient of this chemical treatment barrier by reducing the concentration of the primary oxidizing species in groundwater (i.e., nitrate and dissolved oxygen) and chromium, thereby increasing the longevity of the chemical barrier and helping to diminish the chromium plume.

  6. Apatite deposition and collagen coating effects in Ti-Al-V and Ti-Al-Nb alloys

    NASA Astrophysics Data System (ADS)

    Choi, Y.; Hong, S. I.

    2014-12-01

    The biomimetic deposition rate of apatite for Ti-6Al-4V was found to be greater than that for Ti-6Al-7Nb in regular 1 × Modified SBF. The coating of collagen was found to enhance the biomimetic deposition of apatite on Ti-6Al-4V and Ti-6Al-7Nb. The nucleation and growth of the apatite deposition layer was faster on collagen coated Ti alloys. An interesting observation is that the granular structure became less clear and the nodular boundary became obscure in apatite deposited on the collagen-coated Ti alloys. The ill-defined granular structure may be associated with the presence of more amorphous calcium phosphate. The morphology of apatite nodules was found to be modified by collagen coating and collagen addition.

  7. 100-D Area In Situ Redox Treatability Test for Chromate-Contaminated Groundwater

    SciTech Connect

    Williams, Mark D.; Vermeul, Vincent R.; Szecsody, James E.; Fruchter, Jonathan S.

    2000-10-12

    A treatability test was conducted for the In Situ Redox Manipulation (ISRM) technology at the 100 D Area of the U. S. Department of Energy's Hanford Site. The target contaminant was dissolved chromate in groundwater. The ISRM technology creates a permeable subsurface treatment zone to reduce mobile chromate in groundwater to an insoluble form. The ISRM permeable treatment zone is created by reducing ferric iron to ferrous iron within the aquifer sediments, which is accomplished by injecting aqueous sodium dithionite into the aquifer and then withdrawing the reaction products. The goal of the treatability test was to create a linear ISRM barrier by injecting sodium dithionite into five wells. Well installation and site characterization activities began in spring 1997; the first dithionite injection took place in September 1997. The results of this first injection were monitored through the spring of 1998. The remaining four dithionite injections were carried out in May through July of 1998.These five injections created a reduced zone in the Hanford unconfined aquifer approximately 150 feet in length (perpendicular to groundwater flow) and 50 feet wide. The reduced zone extended over the thickness of the unconfined zone. Analysis of post-emplacement groundwater samples showed concentrations of chromate, in the reduced zone decreased from approximately 1.0 mg/L before the tests to below analytical detection limits (<0.007 mg/L). Chromate concentrations also declined in downgradient monitoring wells to as low as 0.020 mg/L. These data, in addition to results from pre-test reducible iron characterization, indicate the barrier should be effective for 20 to 25 years. The 100-D Area ISRM barrier is being expanded to a length of up to 2,300 ft to capture a larger portion of the chromate plume.

  8. Characteristics and treatability of oil-bearing wastes from aluminum alloy machining operations.

    PubMed

    Chen, Luke; Hsieh, Chueh-Chen; Wetherbee, John; Yang, Chen-Lu

    2008-04-15

    Enomoto Industry Co., exclusively uses water-based cutting fluids in its aluminum alloy machining operations. Since the cost of disposal can be much greater than the cost of purchase, the treatability of spent cutting fluids is becoming a major criterion for cutting fluid selection. Samples were collected from the machining lines at Enomoto's facility to determine their characteristics and evaluate their treatability with centrifugation, chemical coagulation and electrochemical coagulation. As expected, oil and grease (O&G) and total suspended solids (TSS) are the main reasons that spent cutting fluids are prohibited from being discharged into local swage systems. The average O&G found in the spent cutting fluids is 87,354 mg/L with TSS of more than 70,000 mg/L. Both O&G and TSS are the major contributors to the high turbidity of these waste effluents. A centrifuge with a relative centrifugal force of 1318 x g, was able to reduce 60% of the turbidity. By adding the coagulant aluminum chloride, the oil-water emulsion was destabilized, and the turbidity was reduced from 3249 Formazin Attenuation Units (FAU) to around 314 FAU. With freshly generated aluminum ions in the spent cutting fluid, the electrochemical process destabilized the oil-water emulsion system. The coalesced oil droplets were adsorbed onto the highly dispersed aluminum coagulant. The oil-rich sludge that was generated in the operation was then floated to the surface, forming a blanket that was removed by skimming. The electrochemical treatment was able to reduce the turbidity to less than 14 FAU, which is the detection limit of the Hach DR/4000 UV-vis spectrophotometer. PMID:17850956

  9. Treatability test plan for the 200-BP-1 prototype surface barrier

    SciTech Connect

    Not Available

    1993-06-01

    The US Department of Energy (DOE), Hanford Site, in Washington State is organized into numerically designated operational areas including the 100, 200, 300, 400, 600, and 1100 Areas. The US Environmental Protection Agency (EPA), in November of 1989, included the 200 Areas of the Hanford Site on the National Priority List (NPL) under the Comprehensive Environmental Response, compensation, and Liability Act of 1980 (CERCLA). The 200 Area is divided into operable units based on waste disposal information, location, facility, type, and other characteristics. The 200-BP-1 operable unit is one specific site located within the 200 East Area. Inclusion on the NPL initiated the remedial investigation (RI) process for characterizing the nature and extent of contamination and assessing risks to human health and the environment at the 200-BP-1 operable unit. In March of 1990, a remedial investigation/feasibility study (RI/FS) work plan for the 200-BP-1 operable unit was issued (DOE-RL 1990a). The work plan outlined the first phase of site characterization activities, which were completed in March of 1993 with the issuance of Phase I Remedial Investigation Report for the 200-BP-1 Operable Unit (DOE-RL 1993, Draft A). Remedial action objectives outlined in the RI report suggest that a likely remedial action at the 200-BP-1 operable unit could involve the use of a surface barrier. To further evaluate this technology, additional performance and constructability data are needed to implement this remedial action. This test plan describes the general methodology for conducting a prototype barrier treatability study. The objectives of this treatability study are to determine overall performance and constructability data on an actual waste site in conjunction with the Hanford Site Barrier Development Program.

  10. Impact of apatite chemical composition on (U-Th)/He thermochronometry: An atomistic point of view

    NASA Astrophysics Data System (ADS)

    Mbongo Djimbi, Duval; Gautheron, Cécile; Roques, Jérôme; Tassan-Got, Laurent; Gerin, Chloé; Simoni, Eric

    2015-10-01

    The quantification of the different parameters influencing He diffusion in apatite is an important issue for the interpretation of (U-Th)/He thermochronometric ages. Key issues include understanding the role of chemical composition and the mechanism modifying diffusivity by radiation damage, both requiring a realistic description at the atomic level. In this contribution, we restrict ourselves on the influence of the chemical composition especially on the effect of Cl-atoms on the He diffusion in the damage-free apatite crystal. For this purpose, a multi-scale theoretical diffusion study has been conducted using periodic Density Functional Theory calculations for two different apatite compositions (pure fluorine apatite and apatite with one chlorine and 3 fluorine atoms per cell called Cl0.25-apatite) representative of damage-free crystals. Different He insertion sites and diffusion pathways are first investigated. The Density Functional Theory approach coupled to the Nudged Elastic Band method is used to determine the energy barriers between the insertion sites. A statistical method, based on Transition State Theory, is used to compute the jump rate between sites and the different results are used as output for a 3D random walk simulation, which determines the diffusion trajectories and the diffusion coefficients. The calculated diffusion coefficients for pure F-apatite exhibit a slightly anisotropic behavior with an activation energy Ea = 95.5 kJ/mol and a frequency factor D0 = 1.9 × 10-3 cm2/s along the c axis; Ea = 106.1 kJ/mol and D0 = 4.1 × 10-3 cm2/s in the plane orthogonal to c. Closure temperatures for a 60 μm grain radius and 10 °C/Ma cooling rate range from 33 to 36 °C and depend on crystal geometry for a given grain size. Surprisingly, even though He diffusion is strongly blocked across the Cl atoms in Cl0.25-apatite, where Ea is significantly higher (166.7 kJ/mol), He atoms can still diffuse along the c axis through workaround pathways. Closure

  11. Feasibility of using natural fishbone apatite as a substitute for hydroxyapatite in remediating aqueous heavy metals.

    PubMed

    Admassu, W; Breese, T

    1999-10-29

    Fishbone, a natural, apatite rich substance, was examined for suitability as a substitute for hydroxyapatite in the sequestering of aqueous divalent heavy metal ions. The fishbone exhibited lower metal removal capacity than pure hydroxyapatite, due primarily to its purity ( approximately 70% apatite equivalent). In other ways the fishbone behaves in a similar manner as pure hydroxyapatite in the sequestration process. It was observed that it can remove all Pb(2+), Cu(2+), Cd(2+) and Ni(2+) to below detectable levels as measured by inductively coupled plasma atomic absorption, and the rate of reaction with either Zn(2+), Ni(2+), or Pb(2+) was also found to be similar to hydroxyapatite. Also, a two level, three variable full factorial design was performed for the Pb/apatite reaction and both apatites performed similarly. The main difference, besides capacity, was on exposure to high (2.4 mM) Pb concentrations. The fishbone removed less of the Pb(2+) than capacity correction predicted. PMID:10536284

  12. The role of collagen in bone apatite formation in the presence of hydroxyapatite nucleation inhibitors

    PubMed Central

    Nudelman, Fabio; Pieterse, Koen; George, Anne; Bomans, Paul H. H.; Friedrich, Heiner; Brylka, Laura J.; Hilbers, Peter A. J.; de With, Gijsbertus; Sommerdijk, Nico A. J. M.

    2011-01-01

    Bone is a composite material, in which collagen fibrils form a scaffold for a highly organized arrangement of uniaxially oriented apatite crystals1,2. In the periodic 67 nm cross-striated pattern of the collagen fibril3–5, the less dense 40-nm-long gap zone has been implicated as the place where apatite crystals nucleate from an amorphous phase, and subsequently grow6–9. This process is believed to be directed by highly acidic non-collagenous proteins6,7,9–11; however, the role of the collagen matrix12–14 during bone apatite mineralization remains unknown. Here, combining nanometre-scale resolution cryogenic transmission electron microscopy and cryogenic electron tomography15 with molecular modelling, we show that collagen functions in synergy with inhibitors of hydroxyapatite nucleation to actively control mineralization. The positive net charge close to the C-terminal end of the collagen molecules promotes the infiltration of the fibrils with amorphous calcium phosphate (ACP). Furthermore, the clusters of charged amino acids, both in gap and overlap regions, form nucleation sites controlling the conversion of ACP into a parallel array of oriented apatite crystals. We developed a model describing the mechanisms through which the structure, supramolecular assembly and charge distribution of collagen can control mineralization in the presence of inhibitors of hydroxyapatite nucleation. PMID:20972429

  13. Experimental evidence regarding the pressure dependence of fission track annealing in apatite

    NASA Astrophysics Data System (ADS)

    Schmidt, J. S.; Lelarge, M. L. M. V.; Conceicao, R. V.; Balzaretti, N. M.

    2014-03-01

    The main purposes of fission track thermochronology are unravelling the thermal histories of sedimentary basins, determining uplift and denudation rates, identifying the structural evolution of orogenic belts, determining sedimentary provenance, and dating volcanic rocks. The effect of temperature on fission tracks is well known and is used to determine the thermal history; however, the effect of pressure on the stability of tracks is still under debate. The present work aims to understand the role of pressure on the annealing kinetics of apatite fission tracks. The samples of Durango apatite used in our experiments were chosen for their international recognition as a calibration standard for geological dating. Neutron irradiation of the samples, after total annealing of their spontaneous tracks, produced induced tracks with homogeneous densities and lengths. The effect of pressure associated with temperature on fission track annealing was verified by experimental procedures using a hydraulic press of 1000 t with a toroidal chamber profile. The experiments consisted of a combination of applying 2 and 4 GPa with 20,150,190,235, and 290 °C for 1 and 10 h. The annealing rate was analysed by measuring the lengths of the fission tracks after each experiment using optical microscopy. The results demonstrate that the annealing of apatite fission tracks has a pressure dependence for samples subjected to 2 and 4 GPa. However, when extrapolated to pressures of ⩽150 MPa, compatible with the normal geological context in which apatite fission track methodology is broadly used, this dependence becomes insignificant compared to the temperature effect.

  14. Crystal alignment of carbonated apatite in bone and calcified tendon: results from quantitative texture analysis.

    PubMed

    Wenk, H R; Heidelbach, F

    1999-04-01

    Calcified tissue contains collagen associated with minute crystallites of carbonated apatite. In this study, methods of quantitative X-ray texture analysis were used to determine the orientation distribution and texture strength of apatite in a calcified turkey tendon and in trabecular and cortical regions of osteonal bovine ankle bone (metacarpus). To resolve local heterogeneity, a 2 or 10 microm synchrotron microfocus X-ray beam (lambda = 0.78 A) was employed. Both samples revealed a strong texture. In the case of turkey tendon, 12 times more c axes of hexagonal apatite were parallel to the fibril axis than perpendicular, and a axes had rotational freedom about the c axis. In bovine bone, the orientation density of the c axes was three times higher parallel to the surface of collagen fibrils than perpendicular to it, and there was no preferential alignment with respect to the long axis of the bone (fiber texture). Whereas half of the apatite crystallites were strongly oriented, the remaining half had a random orientation distribution. The synchrotron X-ray texture results were consistent with previous analyses of mineral orientation in calcified tissues by conventional X-ray and neutron diffraction and electron microscopy, but gave, for the first time, a quantitative description. PMID:10221548

  15. COMPARISON OF APATITE II™ TREATMENT SYSTEM AT TWO MINES FOR METALS REMOVAL

    EPA Science Inventory

    Two abandoned lead-zinc mine sites, the Nevada Stewart Mine (NSM) and Success Mine, are located within the Coeur d'Alene Mining District, in northern Idaho. An Apatite II™ Treatment System (ATS) was implemented at each site to treat metal-laden water, mainly zinc. In the ATS, f...

  16. Mycorrhizal weathering of apatite as an important calcium source in base-poor forest ecosystems.

    PubMed

    Blum, Joel D; Klaue, Andrea; Nezat, Carmen A; Driscoll, Charles T; Johnson, Chris E; Siccama, Thomas G; Eagar, Christopher; Fahey, Timothy J; Likens, Gene E

    2002-06-13

    The depletion of calcium in forest ecosystems of the northeastern USA is thought to be a consequence of acidic deposition and to be at present restricting the recovery of forest and aquatic systems now that acidic deposition itself is declining. This depletion of calcium has been inferred from studies showing that sources of calcium in forest ecosystems namely, atmospheric deposition and mineral weathering of silicate rocks such as plagioclase, a calcium-sodium silicate do not match calcium outputs observed in forest streams. It is therefore thought that calcium is being lost from exchangeable and organically bound calcium in forest soils. Here we investigate the sources of calcium in the Hubbard Brook experimental forest, through analysis of calcium and strontium abundances and strontium isotope ratios within various soil, vegetation and hydrological pools. We show that the dissolution of apatite (calcium phosphate) represents a source of calcium that is comparable in size to known inputs from atmospheric sources and silicate weathering. Moreover, apatite-derived calcium was utilized largely by ectomycorrhizal tree species, suggesting that mycorrhizae may weather apatite and absorb the released ions directly, without the ions entering the exchangeable soil pool. Therefore, it seems that apatite weathering can compensate for some of the calcium lost from base-poor ecosystems, and should be considered when estimating soil acidification impacts and calcium cycling. PMID:12066181

  17. Infrared spectroscopic characterization of carbonated apatite: a combined experimental and computational study.

    PubMed

    Ren, Fuzeng; Ding, Yonghui; Leng, Yang

    2014-02-01

    A combined experimental and computational approach was employed to investigate the feasibility and effectiveness of characterizing carbonated apatite (CAp) by infrared (IR) spectroscopy. First, an experimental comparative study was conducted to identify characteristic IR vibrational bands of carbonate substitution in the apatite lattice. The IR spectra of pure hydroxyapatite (HA), carbonate adsorbed on the HA surface, a physical mixture of HA and sodium carbonate monohydrate, a physical mixture of HA and calcite, synthetic CAps prepared using three methods (precipitation method, hydrothermal route, and solid-gas reaction at high temperature) and biological apatites (human enamel, human cortical bone, and two animal bones) were compared. Then, the IR vibrational bands of carbonate in CAp were calculated with density functional theory. The experimental study identified characteristic IR bands of carbonate that cannot be generated from surface adsorption or physical mixtures and the results show that the bands at ∼880, 1413, and 1450 cm(-1) should not be used as characteristic bands of CAp since they could result from carbonate adsorbed on the apatite crystals surface or present as a separate phase. The combined experimental and computational study reveals that the carbonate v3 bands at ∼1546 and 1465 cm(-1) are, respectively, the IR signature bands for type A CAp and type B CAp. PMID:23533194

  18. Preparation of fluoride substituted apatite cements as the building blocks for tooth enamel restoration

    NASA Astrophysics Data System (ADS)

    Wei, Jie; Wang, Jiecheng; Liu, Xiaochen; Ma, Jian; Liu, Changsheng; Fang, Jing; Wei, Shicheng

    2011-06-01

    Fluoride substituted apatite cement (fs-AC) was synthesized by using the cement powders of tetracalcium phosphate (TTCP) and sodium fluoride (NaF), and the cement powders were mixed with diluted phosphoric acid (H 3PO 4) as cement liquid to form fs-AC paste. The fs-AC paste could be directly filled into the carious cavities to repair damaged dental enamel. The results indicated that the fs-AC paste was changed into fluorapatite crystals with the atom molar ratio for calcium to phosphorus of 1.66 and the F ion amount of 3 wt% after self-hardening for 2 days. The solubility of fs-AC in Tris-HCl solution (pH 6) was slightly lower than hydroxyapatite cement (HAC) that was similar to the apatite in enamel, indicating the fs-AC was much insensitive to the weakly acidic solution than the apatite in enamel. The fs-AC was tightly combined with the enamel surface because of the chemical reaction between the fs-AC and the apatite in enamel after the caries cavities was filled with fs-AC. The extracts of fs-AC caused no cytotoxicity on L929 cells, which satisfied the relevant criterion on dental biomaterials, revealing good cytocompatibility. The fs-AC had potential prospect for the reconstitution of carious lesion of dental enamel.

  19. The status of strontium in biological apatites: an XANES investigation.

    PubMed

    Bazin, D; Daudon, M; Chappard, Ch; Rehr, J J; Thiaudière, D; Reguer, S

    2011-11-01

    Osteoporosis represents a major public health problem and increases patient morbidity through its association with fragility fractures. Among the different treatments proposed, strontium-based drugs have been shown to increase bone mass in postmenopausal osteoporosis patients and to reduce fracture risk. While the localization of Sr(2+) cations in the bone matrix has been extensively studied, little is known regarding the status of Sr(2+) cations in natural biological apatite. In this investigation the local environment of Sr(2+) cations has been investigated through XANES (X-ray absorption near-edge structure) spectroscopy in a set of pathological and physiological apatites. To assess the localization of Sr(2+) cations in these biological apatites, numerical simulations using the ab initio FEFF9 X-ray spectroscopy program have been performed. The complete set of data show that the XANES part of the absorption spectra may be used as a fingerprint to determine the localization of Sr(2+) cations versus the mineral part of calcifications. More precisely, it appears that a relationship exists between some features present in the XANES part and a Sr(2+)/Ca(2+) substitution process in site (I) of crystal apatite. Regarding the data, further experiments are needed to confirm a possible link between the relationship between the preparation mode of the calcification (cellular activity for physiological calcification and precipitation for the pathological one) and the adsorption mode of Sr(2+) cations (simple adsorption or insertion). Is it possible to draw a line between life and chemistry through the localization of Sr in apatite? The question is open for discussion. A better structural description of these physiological and pathological calcifications will help to develop specific therapies targeting the demineralization process in the case of osteoporosis. PMID:21997917

  20. Ultrastructural analysis of apatite-degrading capability of extended invasive podosomes in resorbing osteoclasts.

    PubMed

    Akisaka, Toshitaka; Yoshida, Astushi

    2016-09-01

    Osteoclasts in culture are non-transformed cell types that spontaneously develop specific cell-adhesion devices such as podosomes. An individual podosome is a complex network of filamentous actin (F-actin) unit structure that collectively, with other proteins, self-organizes as the sealing zone. Major matrix degradation on apatite seems to proceed under the ruffled-border domain, which is an enclosed extracellular compartment tightly sealed off by this sealing zone. Presently we found that usually the top of finger-like projections of the ruffled border reached toward the plane of the apatite surface, where a shallow degradation of apatite took place. Simultaneously, we obtained several pieces of structural evidence indicating that a specific protrusion referred to as an invasive podosome (invadopodium), which was continuous with podosomes derived from the sealing zone, invaded deeply into apatite matrix and degraded it. The F-actin architecture of the invasive podosome - an active extracellular matrix-degrading, actin-rich cell protrusion - could be distinguished from that of other punctate F-actin structures including the individual podosome, sealing zone, and ruffled border projection. Invasive podosomes contained 2 different F-actin populations, i.e., an interconnected meshwork and a parallel array of bundles. The morphological variability of these protrusions was apparent, having a single cylindrical to lamella-shaped cytoskeletal organization. Our present observations strongly suggest that the degradation of apatite substrate-resorbing osteoclasts appears to have been preceded by the combined appearance of ruffled border and invasive podosomes, and also occurred simultaneously with cell migration during an alternating cycle of resorption and migration. PMID:27323283

  1. Functions and requirements for a waste dislodging and conveyance system for the Gunite and Associated Tanks Treatability Study at Oak Ridge National Laboratory

    SciTech Connect

    Potter, J.D.; Mullen, O.D.

    1995-09-01

    Functions and requirements for the Waste Dislodging and Conveyance System to be deployed in Gunite and Associated Tanks (GAAT) and tested and evaluated as a candidate tank waste retrieval technology by the GAAT Treatability Study (GAAT TS).

  2. Radiation damage control on apatite (U-Th)/He dates from the Grand Canyon region, Colorado Plateau

    NASA Astrophysics Data System (ADS)

    Flowers, R. M.; Shuster, D. L.; Wernicke, B. P.; Farley, K. A.

    2007-05-01

    Individual detrital apatite grains from the Esplanade, Coconino, and Moenkopi Formations in the Grand Canyon region of the Colorado Plateau yield (U-Th)/He dates from 104 to 5 Ma. The range of dates within each unit far exceeds analytical uncertainty, but correlates with both He concentration [He] and effective U concentration [eU]. These dates are all significantly younger than the sandstone units, indicating partial to complete He loss following deposition. Recently published laboratory diffusion data suggest that He retentivity in apatite increases with radiation damage. Forward models predict that the consequences of this effect will be manifested most clearly as a correlation between (U-Th)/He dates and the [He] and [eU] in suites of apatites that (1) are characterized by a large span of [eU], and (2) had thermal histories in which sufficient time elapsed for the apatite He diffusion kinetics to diverge prior to reheating and partial resetting. Apatites in the sedimentary units investigated fit these cri teria. Using geologically reasonable deposition, burial, and unroofing histories, simulations that include the effect of radiation damage on apatite He retentivity can reproduce the observed distributions of apatite dates and correlations with parent and daughter concentrations. These results suggest that a span of (U-Th)/He dates positively correlated with [eU] may provide important information regarding a sample's thermal history.

  3. Apatite-forming ability of vinylphosphonic acid-based copolymer in simulated body fluid: effects of phosphate group content.

    PubMed

    Hamai, Ryo; Shirosaki, Yuki; Miyazaki, Toshiki

    2016-10-01

    Phosphate groups on materials surfaces are known to contribute to apatite formation upon exposure of the materials in simulated body fluid and improved affinity of the materials for osteoblast-like cells. Typically, polymers containing phosphate groups are organic matrices consisting of apatite-polymer composites prepared by biomimetic process using simulated body fluid. Ca(2+) incorporation into the polymer accelerates apatite formation in simulated body fluid owing because of increase in the supersaturation degree, with respect to apatite in simulated body fluid, owing to Ca(2+) release from the polymer. However, the effects of phosphate content on the Ca(2+) release and apatite-forming abilities of copolymers in simulated body fluid are rather elusive. In this study, a phosphate-containing copolymer prepared from vinylphosphonic acid, 2-hydroxyethyl methacrylate, and triethylene glycol dimethacrylate was examined. The release of Ca(2+) in Tris-NaCl buffer and simulated body fluid increased as the additive amount of vinylphosphonic acid increased. However, apatite formation was suppressed as the phosphate groups content increased despite the enhanced release of Ca(2+) from the polymer. This phenomenon was reflected by changes in the surface zeta potential. Thus, it was concluded that the apatite-forming ability of vinylphosphonic acid-2-hydroxyethyl methacrylate-triethylene glycol dimethacrylate copolymer treated with CaCl2 solution was governed by surface state rather than Ca(2+) release in simulated body fluid. PMID:27585911

  4. Mechanism of Uranium Sorption by Apatite Materials from a Permeable Reactive Barrier Demonstration at Fry Canyon, Utah

    NASA Astrophysics Data System (ADS)

    Bargar, J. R.; Fuller, C. C.; Davis, J. A.

    2002-12-01

    Ground water at the Fry Canyon, Utah site (pH 7; 4.8 mM alkalinity) is contaminated with uranium (to 20 mg/L) leached from tailings at a now-abandoned ore upgrader facility. An apatite-based chemical reactive barrier (PRB) was installed in the hydrologic flow path at Fry Canyon in 1997 to determine its technological and economic feasibility for ground water remediation. As part of this study, uranium (U(VI)) was reacted with apatite materials, evaluated for use in the PRB, under laboratory conditions. The speciation of U(VI) was subsequently characterized by EXAFS spectroscopy. U(VI) speciation in pelletized bone charcoal apatite recovered from the PRB was also characterized. In carbonate-containing solutions and in ground water, uranium was found to be adsorbed to the apatite materials as apatite-uranyl-carbonate (i.e., "ternary") surface complexes. In carbonate-free solutions, apatite-uranyl-phosphate ternary complexes were found to predominate. At high total uranium concentrations, uranium solubility was limited by precipitation of the uranyl phosphate phase, chernikovite. Uranium solubility was significantly enhanced in the presence of dissolved carbonate. In an apatite-based PRB application, close monitoring will be required to ensure that U(VI) breakthrough does not occur when adsorption equilibrium is reached. The sorptive capacity of the PRB will be affected by the dissolved carbonate concentration of the ground water.

  5. Postmagmatic magnetite-apatite assemblage in mafic intrusions: a case study of dolerite at Olympic Dam, South Australia

    NASA Astrophysics Data System (ADS)

    Apukhtina, Olga B.; Kamenetsky, Vadim S.; Ehrig, Kathy; Kamenetsky, Maya B.; McPhie, Jocelyn; Maas, Roland; Meffre, Sebastien; Goemann, Karsten; Rodemann, Thomas; Cook, Nigel J.; Ciobanu, Cristiana L.

    2016-01-01

    An assemblage of magnetite and apatite is common worldwide in different ore deposit types, including disparate members of the iron-oxide copper-gold (IOCG) clan. The Kiruna-type iron oxide-apatite deposits, a subtype of the IOCG family, are recognized as economic targets as well. A wide range of competing genetic models exists for magnetite-apatite deposits, including magmatic, magmatic-hydrothermal, hydrothermal(-metasomatic), and sedimentary(-exhalative). The sources and mechanisms of transport and deposition of Fe and P remain highly debatable. This study reports petrographic and geochemical features of the magnetite-apatite-rich vein assemblages in the dolerite dykes of the Gairdner Dyke Swarm (~0.82 Ga) that intruded the Roxby Downs Granite (~0.59 Ga), the host of the supergiant Olympic Dam IOCG deposit. These symmetrical, only few mm narrow veins are prevalent in such dykes and comprise besides usually colloform magnetite and prismatic apatite also further minerals (e.g., calcite, quartz). The genetic relationships between the veins and host dolerite are implied based on alteration in the immediate vicinity (~4 mm) of the veins. In particular, Ti-magnetite-ilmenite is partially to completely transformed to titanite and magmatic apatite disappears. We conclude that the mafic dykes were a local source of Fe and P re-concentrated in the magnetite-apatite veins. Uranium-Pb ages for vein apatite and titanite associated with the vein in this case study suggest that alteration of the dolerite and healing of the fractures occurred shortly after dyke emplacement. We propose that in this particular case the origin of the magnetite-apatite assemblage is clearly related to hydrothermal alteration of the host mafic magmatic rocks.

  6. SUMMARY PLAN FOR BENCH-SCALE REFORMER AND PRODUCT TESTING TREATABILITY STUDIES USING HANFORD TANK WASTE

    SciTech Connect

    DUNCAN JB

    2010-08-19

    This paper describes the sample selection, sample preparation, environmental, and regulatory considerations for shipment of Hanford radioactive waste samples for treatability studies of the FBSR process at the Savannah River National Laboratory and the Pacific Northwest National Laboratory. The U.S. Department of Energy (DOE) Hanford tank farms contain approximately 57 million gallons of wastes, most of which originated during the reprocessing of spent nuclear fuel to produce plutonium for defense purposes. DOE intends to pre-treat the tank waste to separate the waste into a high level fraction, that will be vitrified and disposed of in a national repository as high-level waste (HLW), and a low-activity waste (LAW) fraction that will be immobilized for on-site disposal at Hanford. The Hanford Waste Treatment and Immobilization Plant (WTP) is the focal point for the treatment of Hanford tank waste. However, the WTP lacks the capacity to process all of the LAW within the regulatory required timeframe. Consequently, a supplemental LAW immobilization process will be required to immobilize the remainder of the LAW. One promising supplemental technology is Fluidized Bed Steam Reforming (FBSR) to produce a sodium-alumino-silicate (NAS) waste form. The NAS waste form is primarily composed of nepheline (NaAlSiO{sub 4}), sodalite (Nas[AlSiO{sub 4}]{sub 6}Cl{sub 2}), and nosean (Na{sub 8}[AlSiO{sub 4}]{sub 6}SO{sub 4}). Semivolatile anions such as pertechnetate (TcO{sub 4}{sup -}) and volatiles such as iodine as iodide (I{sup -}) are expected to be entrapped within the mineral structures, thereby immobilizing them (Janzen 2008). Results from preliminary performance tests using surrogates, suggests that the release of semivolatile radionuclides {sup 99}Tc and volatile {sup 129}I from granular NAS waste form is limited by Nosean solubility. The predicted release of {sup 99}Tc from the NAS waste form at a 100 meters down gradient well from the Integrated Disposal Facility (IDF

  7. Site sampling and treatability studies for demonstration of WasteChem's asphalt encapsulation technology under EPA's SITE program

    SciTech Connect

    Hubbard, J.; Tsadwa, S.; Wills, N.; Evans, M.

    1990-10-01

    This paper presents a sampling approach that was used to determine whether there were adequate quantities and concentrations of wastes at the Woodland Township Route 532 Site for demonstration of the asphalt encapsulation technology. This paper also presents the result of a bench-scale treatability study on wastes from this site. The preliminary sampling and analysis confirmed most of the types of organic and inorganic contaminants found at the Woodland Township Route 532 site during the remedial investigation (RI). However, the contamination levels varied over relatively short distances across the site from some contaminants. The bench-scale treatability study indicated that, when compared with concentrations in the untreated waste, WasteChem's asphalt encapsulation technology reduced semivolatile organic compound concentrations in the toxicity characteristic leaching procedure extracts of treated wastes. The study also indicated that metals concentrations in the TCLP extracts were lower in the treated wastes than the untreated wastes in some samples and higher in others.

  8. Project management plan for the gunite and associated tanks treatability studies project at Oak Ridge National Laboratory, Oak Ridge, Tennessee

    SciTech Connect

    1995-12-01

    This plan for the Gunite and Associated Tanks (GAAT) Treatability Studies Project satisfies the requirements of the program management plan for the Oak Ridge National Laboratory (ORNL) Environmental Restoration (ER) Program as established in the Program Management Plan for the Martin Marietta Energy Systems, Inc., Oak Ridge National Laboratory Site Environmental Restoration Program. This plan is a subtier of several other ER documents designed to satisfy the US Department of Energy (DOE) Order 4700.1 requirement for major systems acquisitions. This project management plan identifies the major activities of the GAAT Treatability Studies Project; establishes performance criteria; discusses the roles and responsibilities of the organizations that will perform the work; and summarizes the work breakdown structure, schedule, milestones, and cost estimate for the project.

  9. Reduction And Stabilization (Immobilization) Of Pertechnetate To An Immobile Reduced Technetium Species Using Tin(II) Apatite

    SciTech Connect

    Duncan, J. B.

    2012-11-02

    Synthetic tin(II)apatite reduces pertechnetate from the mobile +7 to a non-mobile oxidation state and sequesters the technetium, preventing re-oxidization to mobile +7 state under acidic or oxygenated conditions. Previous work indicated technetium reacted Sn(II)apatite can achieve an ANSI leachability index of 12.8 in Cast Stone. An effect by pH is observed on the distribution coefficient, the highest distribution coefficient being l70,900 observed at pH levels of 2.5 to 10.2. The tin apatite was resistant to releasing technetium under test conditions.

  10. TREATABILITY TEST FOR REMOVING TECHNETIUM-99 FROM 200-ZP-1 GROUNDWATER HANFORD SITE

    SciTech Connect

    PETERSEN SW; TORTOSO AC; ELLIOTT WS; BYRNES ME

    2007-11-29

    The 200-ZP-1 Groundwater Operable Unit (OU) is one of two groundwater OUs located within the 200 West groundwater aggregate area of the Hanford Site. The primary risk-driving contaminants within the 200-ZP-1 OU include carbon tetrachloride and technetium-99 (Tc-99). A pump-and-treat system for this OU was initially installed in 1995 to control the 0.002 kg/m{sup 3} (2000 {micro}g/L) contour of the carbon tetrachloride plume. Carbon tetrachloride is removed from groundwater with the assistance of an air-stripping tower. Ten extraction wells and three injection wells operate at a combined rate of approximately 0.017m{sup 3}/s (17.03 L/s). In 2005, groundwater from two of the extraction wells (299-W15-765 and 299-W15-44) began to show concentrations greater than twice the maximum contaminant level (MCL) of Tc-99 (33,309 beq/m{sup 3} or 900 pCi/L). The Tc-99 groundwater concentrations from all ten of the extraction wells when mixed were more than one-half of the MCL and were slowly increasing. If concentrations continued to rise and the water remained untreated for Tc-99, there was concern that the water re-injected into the aquifer could exceed the MCL standard. Multiple treatment technologies were reviewed for selectively removing Tc-99 from the groundwater. Of the treatment technologies, only ion exchange was determined to be highly selective, commercially available, and relatively low in cost. Through research funded by the U.S. Department of Energy, the ion-exchange resin Purolite{reg_sign} A-530E was found to successfully remove Tc-99 from groundwater, even in the presence of competing anions. For this and other reasons, Purolite{reg_sign} A-530E ion exchange resin was selected for treatability testing. The treatability test required installing resin columns on the discharge lines from extraction wells 299-W15-765 and 299-W15-44. Preliminary test results have concluded that the Purolite{reg_sign} A-530E resin is effective at removing Tc-99 from groundwater to

  11. Deep Vadose Zone Treatability Test for the Hanford Central Plateau. Interim Post-Desiccation Monitoring Results, Fiscal Year 2015

    SciTech Connect

    Truex, Michael J.; Strickland, Christopher E.; Oostrom, Martinus; Johnson, Christian D.; Tartakovsky, Guzel D.; Johnson, Timothy C.; Clayton, Ray E.; Chronister, Glen B.

    2015-09-01

    A field test of desiccation is being conducted as an element of the Deep Vadose Zone Treatability Test Program. The active desiccation portion of the test has been completed. Monitoring data have been collected at the field test site during the post-desiccation period and are reported herein. This is an interim data summary report that includes about 4 years of post-desiccation monitoring data. The DOE field test plan proscribes a total of 5 years of post-desiccation monitoring.

  12. New insights on He diffusion in apatite and implication for (U-Th)/He thermochronology (Invited)

    NASA Astrophysics Data System (ADS)

    Gautheron, C.; Tassan-Got, L.; Gerin, C.; Mbongo, D.; Roques, J.; Oliviero, E.; Bachelet, C.; Simoni, E.

    2013-12-01

    The apatite (U-Th)/He (AHe) system has rapidly become a very popular thermochronometer to constrain exhumation and relief evolution in a variety of geological contexts, as it allows dating and estimating the amount of denudation. However, the interpretation of AHe data depends on a precise knowledge of He diffusion in apatite, which is sensible in the 55 to 120°C range. Several studies suggest that radiation damage generated by U and Th decay can create traps for He atoms, increasing He retention as a function of the number of traps. The radiation damage also anneals with temperature and the amount of damage in an apatite crystal will be a balance between production and annealing, controlled by U-Th concentration, grain chemistry and thermal history (Shuster et al., 2006; Flowers et al., 2009; Gautheron et al., 2009; 2013). However these models are not well constrained and do not fully explain the mechanism of He retention. In order to have a deeper insight on this issue, multidisciplinary studies on apatite combining diffusion experiments by Elastic Recoil Diffusion Analysis (ERDA) with diffusion calculation Density Functional Theory (DFT) were performed. ERDA experiments were conducted on different macro-crystals, and we probed the shape of a He profile implanted into a planar and polished surface of the crystal. The helium profile evolves with temperature and allows the quantification of He diffusivity. Additionally, DFT calculations of a crystal of apatite have been run to find the favored paths of a helium atom between interstitial sites, leading to a computation of the activation energy and the diffusion coefficient. Crystals with different F and Cl compositions, in similar proportion as natural ones, have been investigated and show chemical variations due to steric effects. Using ERDA and DFT approaches, we demonstrate that in addition to the damage, the grain chemistry strongly impacts He diffusivity and needs to be taken into account. Shuster, D., Flowers

  13. Stable isotope record of coexisting apatite and dolomite in Early Cambrian phosphorites, Meishucun section, South China

    NASA Astrophysics Data System (ADS)

    Wegwerth, Antje; Struck, Ulrich; Segl, Monika; Vennemann, Torsten W.; Gehlken, Peer-L.; Heubeck, Christoph; Böttcher, Michael E.

    2010-05-01

    The Precambrian-Cambrian transition forms one of the most dramatic time periods in Earth's history, as global changes in tectonics, climate and chemistry in the atmosphere and oceans favoured the worldwide Cambrian Radiation and a concomitant ecosphere revolution. This time interval is paralleled by the first appearance of the widespread giant phosphorites. The well-known Meishucun section (South China), a former candidate section for the Pc-C boundary, documents phosphorite genesis amongst a rapid biodiversification, immediately following the end of the Precambrian in a low-latitude, shallow-water carbonate shelf. This contribution aims to elucidate the relation between simultaneous phosphorite deposition and global environmental conditions at the Pc-C boundary by using stable carbon and oxygen isotope analyses. Accurate determinations of d13C and d18O values may allow conclusions about ancient ocean circulation, paleo-productivity, paleo-temperatures, and most prominently diagenetic processes. The investigated samples from the Meishucun section basically consist of apatite, dolomite, and quartz that may be further devided into a lower and upper phosphorite as well as an overlying dolostone intervall. Additionally, calcite and siderite occur as minor compounds in some samples. Bulk d13C values of the carbonate fraction correlate with dolomite abundance throughout the section ranging from -4 to 1 per mil. Furthermore, several horizons suggest a relation between d13C values and apatite content, implying lower d13C values in apatites compared to coexisting dolomite. A slight negative d13C excursion at the top of the lower phosphorite coincides with the first appearance of small shelly fossils. Corresponding bulk d18O values generally show a stratigraphic-upward trend towards lower values throughout the record with slightly higher values in dolomite-rich sections. This may either indicate a warming trend during deposition, an isotopic shift in sea water composition

  14. Hydraulic testing plan for the Bear Creek Valley Treatability Study, Oak Ridge Y-12 Plant, Oak Ridge, Tennessee

    SciTech Connect

    1997-09-01

    The Bear Creek Valley (BCV) Treatability Study is intended to provide site-specific data defining potential treatability technologies applicable to contaminated groundwater and surface water. The ultimate goal of this effort is to install a treatment system that will remove uranium, technetium, nitrate, and several metals from groundwater before it reaches Bear Creek. This project directly supports the BCV Feasibility Study. Part of the Treatability Study, Phase II Hydraulic Performance Testing, will produce hydraulic and treatment performance data required to design a long-term treatment system. This effort consists of the installation and testing of two groundwater collection systems: a trench in the vicinity of GW-835 and an angled pumping well adjacent to NT-1. Pumping tests and evaluations of gradients under ambient conditions will provide data for full-scale design of treatment systems. In addition to hydraulic performance, in situ treatment chemistry data will be obtained from monitoring wells installed in the reactive media section of the trench. The in situ treatment work is not part of this test plan. This Hydraulic Testing Plan describes the location and installation of the trench and NT-1 wells, the locations and purpose of the monitoring wells, and the procedures for the pumping tests of the trench and NT-1 wells.

  15. Treatability assessment of polycyclic aromatic hydrocarbons contaminated marine sediments using permanganate, persulfate and Fenton oxidation processes.

    PubMed

    Shih, Yu-Jen; Binh, Nguyen Thanh; Chen, Chiu-Wen; Chen, Chih-Feng; Dong, Cheng-Di

    2016-05-01

    Various chemical oxidation techniques, such as potassium permanganate (KMnO4), sodium persulfate (Na2S2O8), Fenton (H2O2/Fe(2+)), and the modified persulfate and Fenton reagents (activated by ferrous complexes), were carried out to treat marine sediments that were contaminated with polycyclic aromatic hydrocarbons (PAHs) and dredged from Kaohsiung Harbor in Taiwan. Experimental results revealed that KMnO4 was the most effective of the tested oxidants in PAH degradation. Owing to the high organic matter content in the sediment that reduced the efficiencies of Na2S2O8 and regular Fenton reactions, a large excess of oxidant was required. Nevertheless, KH2PO4, Na4P2O7 and four chelating agents (EDTA, sodium citrate, oxalic acid, and sodium oxalate) were utilized to stabilize Fe(II) in activating the Na2S2O8 and Fenton oxidations, while Fe(II)-citrate remarkably promoted the PAH degradation. Increasing the molecular weight and number of rings of PAH did not affect the overall removal efficiencies. The correlation between the effectiveness of the oxidation processes and the physicochemical properties of individual PAH was statistically analyzed. The data implied that the reactivity of PAH (electron affinity and ionization potential) affected its treatability more than did its hydrophobicity (Kow, Koc and Sw), particularly using experimental conditions under which PAHs could be effectively oxidized. PMID:26915591

  16. Treatability study of absorbent polymer waste form for mixed waste treatment

    SciTech Connect

    Herrmann, S. D.; Lehto, M. A.; Stewart, N. A.; Croft, A. D.; Kern, P. W.

    2000-02-10

    A treatability study was performed to develop and characterize an absorbent polymer waste form for application to low level (LLW) and mixed low level (MLLW) aqueous wastes at Argonne National Laboratory-West (ANL-W). In this study absorbent polymers proved effective at immobilizing aqueous liquid wastes in order to meet Land Disposal Restrictions for subsurface waste disposal. Treatment of aqueous waste with absorbent polymers provides an alternative to liquid waste solidification via high-shear mixing with clays and cements. Significant advantages of absorbent polymer use over clays and cements include ease of operations and waste volume minimization. Absorbent polymers do not require high-shear mixing as do clays and cements. Granulated absorbent polymer is poured into aqueous solutions and forms a gel which passes the paint filter test as a non-liquid. Pouring versus mixing of a solidification agent not only eliminates the need for a mixing station, but also lessens exposure to personnel and the potential for spread of contamination from treatment of radioactive wastes. Waste minimization is achieved as significantly less mass addition and volume increase is required of and results from absorbent polymer use than that of clays and cements. Operational ease and waste minimization translate into overall cost savings for LLW and MLLW treatment.

  17. Electrophysiologic features of SYT2 mutations causing a treatable neuromuscular syndrome

    PubMed Central

    Herrmann, David N.; Bansagi, Boglarka; Hasan, Bashar Awwad Shiekh; Lofra, Robert Muni; Logigian, Eric L.; Sowden, Janet E.; Almodovar, Jorge L.; Littleton, J. Troy; Zuchner, Stephan; Horvath, Rita; Lochmüller, Hanns

    2015-01-01

    Objectives: To describe the clinical and electrophysiologic features of synaptotagmin II (SYT2) mutations, a novel neuromuscular syndrome characterized by foot deformities and fatigable ocular and lower limb weakness, and the response to modulators of acetylcholine release. Methods: We performed detailed clinical and neurophysiologic assessment in 2 multigenerational families with dominant SYT2 mutations (c.920T>G [p.Asp307Ala] and c.923G>A [p.Pro308Leu]). Serial clinical and electrophysiologic assessments were performed in members of one family treated first with pyridostigmine and then with 3,4-diaminopyridine. Results: Electrophysiologic testing revealed features indicative of a presynaptic deficit in neurotransmitter release with posttetanic potentiation lasting up to 60 minutes. Treatment with 3,4-diaminopyridine produced both a clinical benefit and an improvement in neuromuscular transmission. Conclusion: SYT2 mutations cause a novel and potentially treatable complex presynaptic congenital myasthenic syndrome characterized by motor neuropathy causing lower limb wasting and foot deformities, with reflex potentiation following exercise and a uniquely prolonged period of posttetanic potentiation. PMID:26519543

  18. Treatability study for the bench-scale solidification of nonincinerable LDR low-level mixed waste

    SciTech Connect

    Gering, K.L.

    1993-01-01

    The focus of this report is the solidification of nonincinerable, land disposal restricted (LDR) low-level mixed waste generated at the Idaho National Engineering Laboratory. Benchscale solidification was performed on samples of this mixed waste, which was done under a Resource Conservation and Recovery Act treatability study. Waste forms included liquids, sludges, and solids, and treatment techniques included the use of conventional Portland cement and sulphur polymer cement (SPC). A total of 113 monoliths were made under the experimental design matrix for this study; 8 of these were ``blank`` monoliths (contained no waste). Thus, 105 monoliths were used to solidify 21.6 kg of mixed waste; 92 were made with Portland cement systems, and 13 were made with SPC. Recipes for all monoliths are given, and suggested recipes (as based on the minimized leaching of toxic components) are summarized. In most cases, the results presented herein indicate that solidification was successful in immobilizing toxic metals, thereby transforming low-level mixed waste into low-level nonhazardous waste. The ultimate goal of this project is to use appropriate solidification techniques, as described in the literature, to transform low-level mixed waste to low-level nonhazardous waste by satisfying pertinent disposal requirements for this waste. Disposal requirements consider the toxicity characteristic leaching procedure tests, a free liquids test, and radiological analyses. This work is meaningful in that it will provide a basis for the disposal of waste that is currently categorized as LDR low-level mixed waste.

  19. Treatability study for the bench-scale solidification of nonincinerable LDR low-level mixed waste

    SciTech Connect

    Gering, K. L.

    1993-01-01

    The focus of this report is the solidification of nonincinerable, land disposal restricted (LDR) low-level mixed waste generated at the Idaho National Engineering Laboratory. Benchscale solidification was performed on samples of this mixed waste, which was done under a Resource Conservation and Recovery Act treatability study. Waste forms included liquids, sludges, and solids, and treatment techniques included the use of conventional Portland cement and sulphur polymer cement (SPC). A total of 113 monoliths were made under the experimental design matrix for this study; 8 of these were blank'' monoliths (contained no waste). Thus, 105 monoliths were used to solidify 21.6 kg of mixed waste; 92 were made with Portland cement systems, and 13 were made with SPC. Recipes for all monoliths are given, and suggested recipes (as based on the minimized leaching of toxic components) are summarized. In most cases, the results presented herein indicate that solidification was successful in immobilizing toxic metals, thereby transforming low-level mixed waste into low-level nonhazardous waste. The ultimate goal of this project is to use appropriate solidification techniques, as described in the literature, to transform low-level mixed waste to low-level nonhazardous waste by satisfying pertinent disposal requirements for this waste. Disposal requirements consider the toxicity characteristic leaching procedure tests, a free liquids test, and radiological analyses. This work is meaningful in that it will provide a basis for the disposal of waste that is currently categorized as LDR low-level mixed waste.

  20. Potentially Treatable Disorder Diagnosed Post Mortem by Exome Analysis in a Boy with Respiratory Distress

    PubMed Central

    Imperatore, Valentina; Mencarelli, Maria Antonietta; Fallerini, Chiara; Bianciardi, Laura; Ariani, Francesca; Furini, Simone; Renieri, Alessandra; Mari, Francesca; Frullanti, Elisa

    2016-01-01

    We highlight the importance of exome sequencing in solving a clinical case of a child who died at 14 months after a series of respiratory crises. He was the half-brother of a girl diagnosed at 7 years with the early-onset seizure variant of Rett syndrome due to CDKL5 mutation. We performed a test for CDKL5 in the boy, which came back negative. Driven by the mother’s compelling need for a diagnosis, we moved forward performing whole exome sequencing analysis. Surprisingly, two missense mutations in compound heterozygosity were identified in the RAPSN gene encoding a receptor-associated protein with a key role in clustering and anchoring nicotinic acetylcholine receptors at synaptic sites. This gene is responsible for a congenital form of myasthenic syndrome, a disease potentially treatable with cholinesterase inhibitors. Therefore, an earlier diagnosis in this boy would have led to a better clinical management and prognosis. Our study supports the key role of exome sequencing in achieving a definite diagnosis in severe perinatal diseases, an essential step especially when a specific therapy is available. PMID:26927095

  1. Validation of an algorithm to determine the primary care treatability of emergency department visits

    PubMed Central

    Jeffery, Molly Moore; Bellolio, M Fernanda; Wolfson, Julian; Abraham, Jean M; Dowd, Bryan E; Kane, Robert L

    2016-01-01

    Objectives We propose a new claims-computable measure of the primary care treatability of emergency department (ED) visits and validate it using a nationally representative sample of Medicare data. Study design and setting This is a validation study using 2011–2012 Medicare claims data for a nationally representative 5% sample of fee-for-service beneficiaries to compare the new measure's performance to the Ballard variant of the Billings algorithm in predicting hospitalisation and death following an ED visit. Outcomes Hospitalisation within 1 day or 1 week of an ED visit; death within 1 week or 1 month of an ED visit. Results The Minnesota algorithm is a strong predictor of hospitalisations and deaths, with performance similar to or better than the most commonly used existing algorithm to assess the severity of ED visits. The Billings/Ballard algorithm is a better predictor of death within 1 week of an ED visit; this finding is entirely driven by a small number of ED visits where patients appear to have been dead on arrival. Conclusions The procedure-based approach of the Minnesota algorithm allows researchers to use the clinical judgement of the ED physician, who saw the patient to determine the likely severity of each visit. The Minnesota algorithm may thus provide a useful tool for investigating ED use in Medicare beneficiaries. PMID:27566637

  2. Potentially Treatable Disorder Diagnosed Post Mortem by Exome Analysis in a Boy with Respiratory Distress.

    PubMed

    Imperatore, Valentina; Mencarelli, Maria Antonietta; Fallerini, Chiara; Bianciardi, Laura; Ariani, Francesca; Furini, Simone; Renieri, Alessandra; Mari, Francesca; Frullanti, Elisa

    2016-01-01

    We highlight the importance of exome sequencing in solving a clinical case of a child who died at 14 months after a series of respiratory crises. He was the half-brother of a girl diagnosed at 7 years with the early-onset seizure variant of Rett syndrome due to CDKL5 mutation. We performed a test for CDKL5 in the boy, which came back negative. Driven by the mother's compelling need for a diagnosis, we moved forward performing whole exome sequencing analysis. Surprisingly, two missense mutations in compound heterozygosity were identified in the RAPSN gene encoding a receptor-associated protein with a key role in clustering and anchoring nicotinic acetylcholine receptors at synaptic sites. This gene is responsible for a congenital form of myasthenic syndrome, a disease potentially treatable with cholinesterase inhibitors. Therefore, an earlier diagnosis in this boy would have led to a better clinical management and prognosis. Our study supports the key role of exome sequencing in achieving a definite diagnosis in severe perinatal diseases, an essential step especially when a specific therapy is available. PMID:26927095

  3. Treatability studies of actual listed waste sludges from the Oak Ridge Reservation (ORR)

    SciTech Connect

    Jantzen, C.M.; Peeler, D.K.; Gilliam, T.M.; Bleier, A.; Spence, R.D.

    1996-05-06

    Oak Ridge National Laboratory (ORNL) and Savannah River Technology Center (SRTC) are investigating vitrification for various low-level and mixed wastes on the Oak Ridge Reservation (ORR). Treatability studies have included surrogate waste formulations at the laboratory-, pilot-, and field-scales and actual waste testing at the laboratory- and pilot-scales. The initial waste to be processing through SRTC`s Transportable Vitrification System (TVS) is the K-1407-B and K-1407-C (B/C) Pond sludge waste which is a RCRA F-listed waste. The B/C ponds at the ORR K-25 site were used as holding and settling ponds for various waste water treatment streams. Laboratory-, pilot-, and field- scale ``proof-of-principle`` demonstrations are providing needed operating parameters for the planned field-scale demonstration with actual B/C Pond sludge waste at ORR. This report discusses the applied systems approach to optimize glass compositions for this particular waste stream through laboratory-, pilot-, and field-scale studies with surrogate and actual B/C waste. These glass compositions will maximize glass durability and waste loading while optimizing melt properties which affect melter operation, such as melt viscosity and melter refractory corrosion. Maximum waste loadings minimize storage volume of the final waste form translating into considerable cost savings.

  4. Treatability study of Tank E-3-1 waste: mixed waste stream SR-W049

    SciTech Connect

    Langton, C.A.

    1997-08-21

    Treatability studies were conducted for tank E-3-1 waste which was previously characterized in WSRC-RP-87-0078. The waste was determined to be mixed waste because it displayed the characteristic of metal toxicity for Hg and Cr and was also contaminated with low levels of radionuclides. Two types of treatments for qualifying this waste suitable for land disposal were evaluated: ion exchange and stabilization with hydraulic materials (portland cement, slag and magnesium phosphate cement). These treatments were selected for testing because: (1) Both treatments can be carried out as in-drum processes., (2) Cement stabilization is the RCRA/LDR best developed available technology (BDAT) for Hg (less than 280 mg/L) and for Cr., and (3) Ion exchange via Mag-Sep is a promising alternative technology for in drum treatment of liquid wastes displaying metal toxicity. Cement stabilization of the E-3-1 material ( supernate and settled solids) resulted in waste forms which passed the TCLP test for both Hg and Cr. However, the ion exchange resins tested were ineffective in removing the Hg from this waste stream. Consequently, cement stabilization is recommended for a treatment of the five drums of the actual waste.

  5. Treatability test of a stacked-tray air stripper for VOC in water

    SciTech Connect

    Pico, T., LLNL

    1998-04-01

    A common strategy for hydraulic containment and mass removal at VOC contaminated sites is `pump and treat (P&T)`. In P&T operations, contaminated ground water is pumped from wells, treated above ground, and discharged. Many P&T remediation systems at VOC sites rely on air stripping technology because VOCs are easily transferred to the vapor phase. In stacked-tray air strippers, contaminated water is aerated while it flows down through a series of trays. System operations at LLNL are strictly regulated by the California and federal Environmental Protection Agencies (Cal/EPA and EPA), the Bay Area Air Quality Management District (BAAQMD), the California Regional Water Quality Control Board (RWQCB) and the Department of Toxic Substances Control (DTSC). These agencies set discharge limits, require performance monitoring, and assess penalties for non-compliance. National laboratories are also subject to scrutiny by the public and other government agencies. This extensive oversight makes it necessary to accurately predict field treatment performance at new extraction locations to ensure compliance with all requirements prior to facility activation. This paper presents treatability test results for a stacked- tray air stripper conducted at LLNL and compares them to the vendor`s modeling software results.

  6. LABORATORY REPORT ON THE REDUCTION AND STABILIZATION (IMMOBILIZATION) OF PERTECHNETATE TO TECHNETIUM DIOXIDE USING TIN(II)APATITE

    SciTech Connect

    DUNCAN JB; HAGERTY K; MOORE WP; RHODES RN; JOHNSON JM; MOORE RC

    2012-06-01

    This effort is part of the technetium management initiative and provides data for the handling and disposition of technetium. To that end, the objective of this effort was to challenge tin(II)apatite (Sn(II)apatite) against double-shell tank 241-AN-105 simulant spiked with pertechnetate (TcO{sub 4}{sup -}). The Sn(II)apatite used in this effort was synthesized on site using a recipe developed at and provided by Sandia National Laboratories; the synthesis provides a high quality product while requiring minimal laboratory effort. The Sn(II)apatite reduces pertechnetate from the mobile +7 oxidation state to the non-mobile +4 oxidation state. It also sequesters the technetium and does not allow for re-oxidization to the mo bile +7 state under acidic or oxygenated conditions within the tested period oftime (6 weeks). Previous work (RPP-RPT-39195, Assessment of Technetium Leachability in Cement-Stabilized Basin 43 Groundwater Brine) indicated that the Sn(II)apatite can achieve an ANSI leachability index in Cast Stone of 12.8. The technetium distribution coefficient for Sn(II)apatite exhibits a direct correlation with the pH of the contaminated media. Table A shows Sn(II)apatite distribution coefficients as a function of pH. The asterisked numbers indicate that the lower detection limit of the analytical instrument was used to calculate the distribution coefficient as the concentration of technetium left in solution was less than the detection limit. The loaded sample (200 mg of Sn(II)apatite loaded with O.311 mg of Tc-99) was subjected to different molarities of nitric acid to determine if the Sn(II)apatite would release the sequestered technetium. The acid was allowed to contact for 1 minute with gentle shaking ('1st wash'); the aqueous solution was then filtered, and the filtrate was analyzed for Tc-99. Table B shows the results ofthe nitric acid exposure. Another portion of acid was added, shaken for a minute, and filtered ('2nd wash'). The technetium-loaded Sn(II)apatite

  7. FTIR monitoring of the growth of the carbonate containing apatite layers from simulated and natural body fluids

    NASA Astrophysics Data System (ADS)

    Stoch, A.; Jastrz ębski, W.; Brożek, A.; Trybalska, B.; Cichocińska, M.; Szarawara, E.

    1999-11-01

    The aim of this work is to perform such a chemical modification of the implant that in vivo conditions on its surface, heterogeneous nucleation of apatite from the body fluid could be easily induced and then its growth successfully performed. The laboratory experiments were carried out with carbon-carbon biocomposites and carbon needled clothes. The surface of carbon was coated with the sol-gel silica or calcium silicate layer and then, under physiological conditions, thermostatically soaked in the synthetic or natural body fluid. Successive steps of the apatite growth were monitored by infrared spectroscopy. It was found that the nucleation and growth of carbonate containing apatite took place at the surface and was more effective on silica-calcium than on silica substrate. The natural body fluid, compared with synthetic body fluid much enhanced the apatite precipitation. This observation supports suggestion that also proteins can act as nucleation centres.

  8. Hydrogen and carbon abundances and isotopic ratios in apatite from alkaline intrusive complexes, with a focus on carbonatites

    NASA Astrophysics Data System (ADS)

    Nadeau, Serge L.; Epstein, Samuel; Stolper, Edward

    1999-06-01

    We report H and C contents and δD and δ 13C values of apatites from 15 alkaline intrusive complexes ranging in age from 110 Ma to 2.6 Ga. Sampling focused on carbonatites, but included silicate rocks as well. Heating at temperatures up to 1500°C is needed to extract fully H 2O and CO 2 from these apatites. Apatites from carbonatite-rich intrusive complexes contain 0.2-1.1 wt% H 2O and 0.05-0.70 wt% CO 2; apatites from two silicate-rich alkaline complexes with little or no carbonatite are generally poorer in both volatile components (0.1-0.2% H 2O and 0.01-0.11% CO 2). D/H ratios in apatites from these rocks are bimodally distributed: group I (δD = -51 to -74‰) and group II (δD = -88 to -104‰). We suggest that the δD values of group I apatites represent primitive, mantle-derived values and that the group II apatites crystallized from degassed magmas, resulting in lower H 2O contents and δD values. Although many factors influence the extent of degassing, the depth of emplacement could represent a major control. In contrast to H 2O contents and δD values, CO 2 contents and δ 13C values of gas released at high temperatures from multiple aliquots of these apatite samples are variable. This suggests the presence of more than one C-bearing component in these apatites, one of which is proposed to be dissolved carbonate; the other, with δ 13C ˜<-25‰, could be associated with hydrocarbons. Group I apatites have δD values similar to those of primitive, mantle-derived basaltic magmas and overlap with (but cover a narrower range than) mantle-derived mica, amphibole, and whole rocks. δ 13C values also overlap typical upper mantle. These results suggest that igneous apatites can retain their primary δD and δ 13C values.

  9. Osteoclastic resorption of bone-like apatite formed on a plastic disk as an in vitro assay system.

    PubMed

    Matsuoka, H; Nakamura, T; Takadama, H; Yamada, S; Tamura, J; Okada, Y; Oka, M; Kokubo, T

    1998-11-01

    We have investigated the applicability of a simple and inexpensive osteoclastic assay system using bone-like apatite-coated polyethyleneterephthalate (PET) disks. A 1 microm thick apatite layer, uniform and homogeneous bone-mineral-like with no organic components, was made on PET disks using a biomimetic process. As substrates for an osteoclastic assay, these coated disks were compared with dentine as well as with bone-like or heat-treated apatite of various thicknesses on apatite- and wollastonite-containing glass ceramic (A-W GC) disks. The unfractionated bone cells, including osteoclasts, of a neonatal rabbit were seeded onto these substrates. By scanning electron microscopic examination, the resorption lacunae of the thick bone-like apatite clearly showed track-like shapes at various depths, similar to those of dentine although the border between the A-W GC and the apatite was unclear. In contrast, those of heat-treated apatite showed small and shallow shapes with irregular margins, quite different from those of dentine. By reducing the thickness of bone-like apatite to 1 microm as well as using PET as its substrate, the margins of the resorption lacunae became quite clear, and with the use of phase-contrast microscopy during culture, osteoclasts and resorption pits could be precisely observed. The resorbed area, easily measured with the aid of bright-field microscopy and an image analyzer, was found to have increased in a time-dependent manner and at the end of 4 days of culture was not statistically different from that of dentine. PMID:9773824

  10. A temporal record of pre-eruptive magmatic volatile contents at Campi Flegrei: Insights from texturally-constrained apatite analyses

    NASA Astrophysics Data System (ADS)

    Stock, Michael J.; Isaia, Roberto; Humphreys, Madeleine C. S.; Smith, Victoria C.; Pyle, David M.

    2016-04-01

    Apatite is capable of incorporating all major magmatic volatile species (H2O, CO2, S, Cl and F) into its crystal structure. Analysis of apatite volatile contents can be related to parental magma compositions through the application of pressure and temperature-dependent exchange reactions (Piccoli and Candela, 1994). Once included within phenocrysts, apatite inclusions are isolated from the melt and preserve a temporal record of magmatic volatile contents in the build-up to eruption. In this work, we measured the volatile compositions of apatite inclusions, apatite microphenocrysts and pyroxene-hosted melt inclusions from the Astroni 1 eruption of Campi Flegrei, Italy (Stock et al. 2016). These data are coupled with magmatic differentiation models (Gualda et al., 2012), experimental volatile solubility data (Webster et al., 2014) and thermodynamic models of apatite compositional variations (Piccoli and Candela, 1994) to decipher pre-eruptive magmatic processes. We find that apatite halogen/OH ratios decreased through magmatic differentiation, while melt inclusion F and Cl concentrations increased. Melt inclusion H2O contents are constant at ~2.5 wt%. These data are best explained by volatile-undersaturated differentiation over most of the crystallisation history of the Astroni 1 melt, with melt inclusion H2O contents reset at shallow levels during ascent. Given the high diffusivity of volatiles in apatite (Brenan, 1993), the preservation of volatile-undersaturated melt compositions in microphenocrysts suggests that saturation was only achieved 10 - 103 days before eruption. We suggest that late-stage transition into a volatile-saturated state caused an increase in magma chamber overpressure, which ultimately triggered the Astroni 1 eruption. This has major implications for monitoring of Campi Flegrei and other similar volcanic systems. Piccoli and Candela, 1994. Am. J. of Sc., 294, 92-135. Stock et al., 2016, Nat. Geosci. Gualda et al., 2012. J. Pet., 53, 875

  11. Influence of disodium EDTA on the nucleation and growth of struvite and carbonate apatite

    NASA Astrophysics Data System (ADS)

    Prywer, Jolanta; Olszynski, Marcin

    2013-07-01

    The effect of disodium EDTA, as an additive, on the crystallization of struvite and carbonate apatite was studied. The growth of struvite crystals and carbonate apatite occurred in the solution of artificial urine at 37 °C and at the condition emulating real urinary tract infection. The results demonstrate that the addition of disodium EDTA increases the induction time and decreases the growth efficiency compared to the baseline (without disodium EDTA). The struvite crystal mean and median diameters were found to decrease in the presence of disodium EDTA but the crystal morphology and habit remain almost unchanged. Disodium EDTA has demonstrated its potential to be further investigated in the presence of bacteria and in vivo conditions.

  12. Electrospun Nanostructured Fibers of Collagen-Biomimetic Apatite on Titanium Alloy

    PubMed Central

    Iafisco, Michele; Foltran, Ismaela; Sabbatini, Simona; Tosi, Giorgio; Roveri, Norberto

    2012-01-01

    Titanium and its alloys are currently the mainly used materials to manufacture orthopaedic implants due to their excellent mechanical properties and corrosion resistance. Although these materials are bioinert, the improvement of biological properties (e.g., bone implant contact) can be obtained by the application of a material that mimics the bone extracellular matrix. To this aim, this work describes a new method to produce nanostructured collagen-apatite composites on titanium alloy substrate, by combining electrospinning and biomimetic mineralization. The characterization results showed that the obtained mineralized scaffolds have morphological, structural, and chemical compositional features similar to natural bone extracellular matrix. Finally, the topographic distribution of the chemical composition in the mineralized matrix evaluated by Fourier Transform Infrared microspectroscopy demonstrated that the apatite nanocrystals cover the collagen fibers assembled by the electrospinning. PMID:22400013

  13. Apatite 4He/3He and (U-Th)/He evidence for an ancient Grand Canyon.

    PubMed

    Flowers, R M; Farley, K A

    2012-12-21

    The Grand Canyon is one of the most dramatic features on Earth, yet when and why it was carved have been controversial topics for more than 150 years. Here, we present apatite (4)He/(3)He thermochronometry data from the Grand Canyon basement that tightly constrain the near-surface cooling history associated with canyon incision. (4)He/(3)He spectra for eastern Grand Canyon apatites of differing He date, radiation damage, and U-Th zonation yield a self-consistent cooling history that substantially validates the He diffusion kinetic model applied here. Similar data for the western Grand Canyon provide evidence that it was excavated to within a few hundred meters of modern depths by ~70 million years ago (Ma), in contrast to the conventional model in which the entire canyon was carved since 5 to 6 Ma. PMID:23196906

  14. Apatite 4He/3He and (U-Th)/He Evidence for an Ancient Grand Canyon

    NASA Astrophysics Data System (ADS)

    Flowers, R. M.; Farley, K. A.

    2012-12-01

    The Grand Canyon is one of the most dramatic features on Earth, yet when and why it was carved have been controversial topics for more than 150 years. Here, we present apatite 4He/3He thermochronometry data from the Grand Canyon basement that tightly constrain the near-surface cooling history associated with canyon incision. 4He/3He spectra for eastern Grand Canyon apatites of differing He date, radiation damage, and U-Th zonation yield a self-consistent cooling history that substantially validates the He diffusion kinetic model applied here. Similar data for the western Grand Canyon provide evidence that it was excavated to within a few hundred meters of modern depths by ~70 million years ago (Ma), in contrast to the conventional model in which the entire canyon was carved since 5 to 6 Ma.

  15. Sol-gel synthesis of a multifunctional, hierarchically porous silica/apatite composite.

    PubMed

    Andersson, Jenny; Areva, Sami; Spliethoff, Bernd; Lindén, Mika

    2005-12-01

    In this study, a degradable, hierarchically porous silica/apatite composite material is developed from a simple low-temperature synthesis. Mesoporosity is induced in the silica portion by the use of supramolecular templating. The template is further removed by calcination. Firstly, hydroxyapatite is synthesized through a sol-gel method at near room temperature conditions. After the mineralization process, the crystal surface is coated with a mesoporous silica matrix using the templates already present in the bulk solution. The material is characterized by XRD, N(2)-sorption, FT-IR, SEM/EDS, and TEM. The coating layer is distributed fairly homogeneously over the apatite surface and the coating thickness is easily adjustable and dependent on the amount of added silica precursor. The hybrid material is shown to efficiently induce calcium phosphate formation under in vitro conditions and simultaneously work as a carrier system for drugs. PMID:15993485

  16. Determination of the oxidation state of uranium in apatite and phosphorite deposits

    USGS Publications Warehouse

    Clarke, R.S., Jr.; Altschuler, Z.S.

    1958-01-01

    Geological and mineralogical evidence indicate that the uranium present in apatite may proxy for calcium in the mineral structure as U(IV). An experimental investigation was conducted and chemical evidence was obtained that establishes the presence of U(IV) in apatite. The following analytical procedure was developed for the determination of U(IV). Carbonatefluorapatite is dissolved in 1.5 M orthophosphoric acid at a temperature of 5??C or slightly below and fluorapatite is dissolved in cold 1.2 M hydrochloric acid (approximately 5??C) containing 1.5 g of hydroxylamine hydrochloride per 100 ml. Uranium(IV) is precipitated by cupferron using titanium as a carrier. The uranium in the precipitate is separated by use of the ethyl acetate extraction procedure and determined fluorimetrically. The validity and the limitations of the method have been established by spike experiments. ?? 1958.

  17. Phosphate-induced metal stabilization: Use of apatite and bone char for the removal of soluble radionuclides in authentic and simulated DOE groundwater

    SciTech Connect

    Bostick, W.D.; Jarabek, R.J.; Conca, J.L.

    1999-07-01

    The apatite group of minerals is a family of calcium phosphate phases. Apatite is the principal component of bone tissue, and it also occurs naturally as mineral deposits in the geosphere. Bone char is calcined (coked) animal bone, containing activated carbon as well as calcium phosphate mineral phases. Apatite II{trademark} is a more reactive form of apatite, supplied by UFA Ventures, Inc., at a cost of approximately 1/4 that of commercial bone char. Apatite is shown to be effective for the removal of select heavy metal impurities in groundwater. Previous investigations have demonstrated that apatite is an effective medium for the stabilization of soluble lead, cadmium, and zinc from mine waste leachate by the formation of highly insoluble precipitate phases. The performance of bone char and apatite II are compared with other candidate sorption media (including granular activated carbon and anion exchange resin) for the removal of soluble uranyl ion in synthetic DOE Site groundwater supplemented with varying levels of interfering nitrate ion. Apatite II has a greater affinity for U(VI), especially in the presence of nitrate ion, as evidenced by a larger value for the conditional distribution coefficient (Kd) in batch test experiments. Contact of uranyl nitrate solution with apatite II is shown to produce highly insoluble mineral phases of the autunite group (calcium uranyl phosphate hydrates). Apatite II is also demonstrated to be moderately effective for the removal of soluble radioactive isotopes of strontium, but not cesium, when these ions are supplemented into authentic DOE Site groundwater.

  18. Enhanced apatite formation on Ti metal heated in PO2-controlled nitrogen atmosphere.

    PubMed

    Hashimoto, Masami; Hayashi, Kazumi; Kitaoka, Satoshi

    2013-10-01

    The oxynitridation of biomedical titanium metal under a precisely regulated oxygen partial pressure (PO2) of 10(-14)Pa in nitrogen atmosphere at 973 K for 1 h strongly enhanced apatite formation compared with that on Ti heated in air. The factors governing the high apatite-forming ability are discussed from the viewpoint of the surface properties of Ti heated under a PO2 of 10(-14)Pa in nitrogen atmosphere determined from X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and zeta potential measurements. Nitrogen (N)-doped TiO2 (interstitial N) was formed on pure Ti heated under a PO2 of 10(-14)Pa in nitrogen atmosphere at 973 K. The XPS O1s main peak shifted toward a lower binding energy upon heating under a PO2 of 10(-14)Pa. This shift may be due to the formation of oxygen vacancies. This Ti surface had a positive zeta potential of approximately 20 mV. According to time-of-flight secondary ion mass spectroscopy results, PO4(3-) ions were predominantly adsorbed on Ti soaked in simulated body fluid (SBF) after heat treatment, followed by calcium ions. It was concluded that the apatite formation kinetics can be described using the Avrami-Erofeev equation with an Avrami index of n=2, which implies the instantaneous nucleation of apatite on the surface of Ti soaked in SBF after heat treatment at 973 K under a PO2 of 10(-14)Pa. PMID:23910327

  19. Novel bioactive Fe-based metallic glasses with excellent apatite-forming ability.

    PubMed

    Qin, Chunling; Hu, Qingfeng; Li, Yongyan; Wang, Zhifeng; Zhao, Weimin; Louzguine-Luzgin, Dmitri V; Inoue, Akihisa

    2016-12-01

    We demonstrate, for the first time, that the (Fe0.75B0.15Si0.1)100-xNbx (x=0, 1 and 3at.%) metallic glasses without toxic and allergic elements exhibit excellent apatite-forming ability in simulated body fluids (SBF), which is expected to be a new generation of biomaterials in stents and orthopedic implants. For the alloys without any surface treatment, spherical particles corresponding to octacalcium phosphate are spontaneously nucleated and precipitated throughout the alloy surface after immersion only for 1day, indicating that the present alloys possess an unusual high bioactivity. During the subsequent in-vitro immersion for 3days, SEM image reveals the typical 'cauliflower' morphology of bone-like hydroxyapatite (HA) with Ca/P ratio of 1.65. In addition, it is surprising to find that the in-vitro SBF immersion not only leads to the formation and growth of the apatite layer but also causes the progressive development of the underlying alloy substrate. Moreover, for the alloys immersed for 3 or 9days, the substrate alloy just beneath the apatite layer consists of a hierarchical nano/macro-porous structure through selective dissolution of the active components Fe and B in the surface. XPS analysis indicates that the apatite nucleation on the present alloys in SBF is attributed to the specific dissolution properties of the present alloys and the fast formation of Si-OH and Fe-OH or Nb-OH functional groups, followed by combination of these groups with Ca(2+) and phosphate ions. PMID:27612742

  20. An evaluation of the reactivity of synthetic and natural apatites in the presence of aqueous metals.

    PubMed

    Dybowska, Agnieszka; Manning, David A C; Collins, Matthew J; Wess, Timothy; Woodgate, Stephen; Valsami-Jones, Eugenia

    2009-04-01

    Metal removal from contaminated effluents was examined following reaction with natural apatites of biological and geological origin or a synthetic hydroxylapatite (HAP). Mammalian meat and bone meal (MBM), a by-product from meat industry, was the biological apatite source. The effect of incineration on metal removal capacity of MBM and HAP was also examined. The reactivity of apatites for all tested metals (Pb, Cd, Cu and Zn) followed the general order: synthetic > biological > mineral. For all apatites tested, Pb was removed best and preferentially from multi-metal solutions. MBM and HAP (0.5 g solid) removed Pb completely from both highly concentrated single metal solutions (50 ml, 1000 mg/L Pb) and from multi-metal solutions (50 ml) with 100 mg/L each of Cd, Cu and Zn in addition to Pb. The incineration of MBM (725 degrees C and 850 degrees C) reduced significantly its capacity for removal of Zn (by 47%, from 56 mg/g to 9 mg/g) and Cd (by 38%, from 53 mg/g to 13 mg/g) in particular and to a lesser extent for Cu (by 14%, from 61 mg/g to 46 mg/g) while the removal of Pb was not affected (100 mg/g). The same pattern was observed for incinerated HAP. SEM and XRD analysis indicated that HAP reacted with the metals by precipitation of pure metal phosphates--Pb hydroxylapatite, Zn phosphate (hopeite), a Cd phosphate (identified only by ED-SEM) and Cu phosphate (libenthenite). PMID:19187953

  1. Apatite coating of electrospun PLGA fibers using a PVA vehicle system carrying calcium ions.

    PubMed

    Kim, In Ae; Rhee, Sang-Hoon

    2010-01-01

    A novel method to coat electrospun poly(D,L-lactic-co-glycolic acid) (PLGA) fiber surfaces evenly and efficiently with low-crystalline carbonate apatite crystals using a poly(vinyl alcohol) (PVA) vehicle system carrying calcium ions was presented. A non-woven PLGA fabric was prepared by electrospinning: a 10 wt% PLGA solution was prepared using 1,1,3,3-hexafluoro-2-propanol as a solvent and electrospun under a electrical field of 1 kV/cm using a syringe pump with a flowing rate of 3 ml/h. The non-woven PLGA fabric, 12 mm in diameter and 1 mm in thickness, was cut and then coated with a PVA solution containing calcium chloride dihydrate (specimen PPC). As controls, pure non-woven PLGA fabric (specimen P) and fabric coated with a calcium chloride dihydrate solution without PVA (specimen PC) were also prepared. Three specimens were exposed to simulated body fluid for 1 week and this exposure led to form uniform and complete apatite coating layer on the fiber surfaces of specimen PPC. However, no apatite had formed to the fiber surfaces of specimen P and only inhomogeneous coating occurred on the fiber surfaces of specimen PC. These results were explained in terms of the calcium chelating and adhesive properties of PVA vehicle system. The practical implication of the results is that this method provides a simple but efficient technique for coating the fiber surface of an initially non-bioactive material with low-crystalline carbonate apatite. PMID:20507712

  2. Hanford 100-N Area In Situ Apatite and Phosphate Emplacement by Groundwater and Jet Injection: Geochemical and Physical Core Analysis

    SciTech Connect

    Szecsody, James E.; Vermeul, Vincent R.; Fruchter, Jonathan S.; Williams, Mark D.; Rockhold, Mark L.; Qafoku, Nikolla; Phillips, Jerry L.

    2010-07-01

    The purpose of this study is to evaluate emplacement of phosphate into subsurface sediments in the Hanford Site 100-N Area by two different technologies: groundwater injection of a Ca-citrate-PO4 solution and water-jet injection of sodium phosphate and/or fish-bone apatite. In situ emplacement of phosphate and apatite adsorbs, then incorporates Sr-90 into the apatite structure by substitution for calcium. Overall, both technologies (groundwater injection of Ca-citrate-PO4) and water-jet injection of sodium phosphate/fish-bone apatite) delivered sufficient phosphate to subsur¬face sediments in the 100-N Area. Over years to decades, additional Sr-90 will incorporate into the apatite precipitate. Therefore, high pressure water jetting is a viable technology to emplace phosphate or apatite in shallow subsurface sediments difficult to emplace by Ca-citrate-PO4 groundwater injections, but further analysis is needed to quantify the relevant areal extent of phosphate deposition (in the 5- to 15-ft distance from injection points) and cause of the high deposition in finer grained sediments.

  3. Formation of Apatite Coatings on an Artificial Ligament Using a Plasma- and Precursor-Assisted Biomimetic Process

    PubMed Central

    Mutsuzaki, Hirotaka; Yokoyama, Yoshiro; Ito, Atsuo; Oyane, Ayako

    2013-01-01

    A plasma- and precursor-assisted biomimetic process utilizing plasma and alternate dipping treatments was applied to a Leed-Keio artificial ligament to produce a thin coating of apatite in a supersaturated calcium phosphate solution. Following plasma surface modification, the specimen was alternately dipped in calcium and phosphate ion solutions three times (alternate dipping treatment) to create a precoating containing amorphous calcium phosphate (ACP) which is an apatite precursor. To grow an apatite layer on the ACP precoating, the ACP-precoated specimen was immersed for 24 h in a simulated body fluid with ion concentrations approximately equal to those in human blood plasma. The plasma surface modification was necessary to create an adequate apatite coating and to improve the coating adhesion depending on the plasma power density. The apatite coating prepared using the optimized conditions formed a thin-film that covered the entire surface of the artificial ligament. The resulting apatite-coated artificial ligament should exhibit improved osseointegration within the bone tunnel and possesses great potential for use in ligament reconstructions. PMID:24048251

  4. Combinatorial MAPLE deposition of antimicrobial orthopedic maps fabricated from chitosan and biomimetic apatite powders.

    PubMed

    Visan, A; Stan, G E; Ristoscu, C; Popescu-Pelin, G; Sopronyi, M; Besleaga, C; Luculescu, C; Chifiriuc, M C; Hussien, M D; Marsan, O; Kergourlay, E; Grossin, D; Brouillet, F; Mihailescu, I N

    2016-09-10

    Chitosan/biomimetic apatite thin films were grown in mild conditions of temperature and pressure by Combinatorial Matrix-Assisted Pulsed Laser Evaporation on Ti, Si or glass substrates. Compositional gradients were obtained by simultaneous laser vaporization of the two distinct material targets. A KrF* excimer (λ=248nm, τFWHM=25ns) laser source was used in all experiments. The nature and surface composition of deposited materials and the spatial distribution of constituents were studied by SEM, EDS, AFM, GIXRD, FTIR, micro-Raman, and XPS. The antimicrobial efficiency of the chitosan/biomimetic apatite layers against Staphylococcus aureus and Escherichia coli strains was interrogated by viable cell count assay. The obtained thin films were XRD amorphous and exhibited a morphology characteristic to the laser deposited structures composed of nanometric round shaped grains. The surface roughness has progressively increased with chitosan concentration. FTIR, EDS and XPS analyses indicated that the composition of the BmAp-CHT C-MAPLE composite films gradually modified from pure apatite to chitosan. The bioevaluation tests indicated that S. aureus biofilm is more susceptible to the action of chitosan-rich areas of the films, whilst the E. coli biofilm proved more sensible to areas containing less chitosan. The best compromise should therefore go, in our opinion, to zones with intermediate-to-high chitosan concentration which can assure a large spectrum of antimicrobial protection concomitantly with a significant enhancement of osseointegration, favored by the presence of biomimetic hydroxyapatite. PMID:27418570

  5. Apatite Formation from Amorphous Calcium Phosphate and Mixed Amorphous Calcium Phosphate/Amorphous Calcium Carbonate.

    PubMed

    Ibsen, Casper J S; Chernyshov, Dmitry; Birkedal, Henrik

    2016-08-22

    Crystallization from amorphous phases is an emerging pathway for making advanced materials. Biology has made use of amorphous precursor phases for eons and used them to produce structures with remarkable properties. Herein, we show how the design of the amorphous phase greatly influences the nanocrystals formed therefrom. We investigate the transformation of mixed amorphous calcium phosphate/amorphous calcium carbonate phases into bone-like nanocrystalline apatite using in situ synchrotron X-ray diffraction and IR spectroscopy. The speciation of phosphate was controlled by pH to favor HPO4 (2-) . In a carbonate free system, the reaction produces anisotropic apatite crystallites with large aspect ratios. The first formed crystallites are highly calcium deficient and hydrogen phosphate rich, consistent with thin octacalcium phosphate (OCP)-like needles. During growth, the crystallites become increasingly stoichiometric, which indicates that the crystallites grow through addition of near-stoichiometric apatite to the OCP-like initial crystals through a process that involves either crystallite fusion/aggregation or Ostwald ripening. The mixed amorphous phases were found to be more stable against phase transformations, hence, the crystallization was inhibited. The resulting crystallites were smaller and less anisotropic. This is rationalized by the idea that a local phosphate-depletion zone formed around the growing crystal until it was surrounded by amorphous calcium carbonate, which stopped the crystallization. PMID:27460160

  6. Deposition of substituted apatites with anticolonizing properties onto titanium surfaces using a novel blasting process.

    PubMed

    O'Sullivan, C; O'Hare, P; O'Leary, N D; Crean, A M; Ryan, K; Dobson, A D W; O'Neill, L

    2010-10-01

    A series of doped apatites have been deposited onto titanium (V) substrates using a novel ambient temperature blasting process. The potential of these deposited doped apatites as non-colonizing osteoconductive coatings has been evaluated in vitro. XPS, EDX, and gravimetric analysis demonstrated that a high degree of coating incorporation was observed for each material. The modified surfaces were found to produce osteoblast proliferation comparable to, or better than, a hydroxyapatite finish. Promising levels of initial microbial inhibition were observed from the Sr- and Ag-doped surfaces, with the strontium showing prolonged ability to reduce bacteria numbers over a 30-day period. Ion elution profiles have been characterized and linked to the microbial response and based on the results obtained, mechanisms of kill have been suggested. In this study, the direct contact of coated substrate surfaces with microbes was observed to be a significant contributing factor to the antimicrobial performance and the anticolonizing activity. The silver substituted apatite was observed to out-perform both the SrA and ZnA in terms of biofilm inhibition. PMID:20737556

  7. In vitro apatite formation on porous anodic alumina induced by a phosphorylation treatment.

    PubMed

    Li, Xiaohong; Ni, Siyu; Webster, Thomas J

    2014-09-01

    In this study, a phosphorylation treatment of porous anodic alumina (PAA) was performed by wet impregnation in phosphoric acid and a subsequent heat treatment. The PAA and phosphorylated PAA specimens were analyzed using a field emission scanning electron microscope, an energy-dispersive X-ray spectrometer, and Fourier transform infrared spectroscopy. The apatite-forming ability of the phosphorylated PAA was evaluated by soaking the specimens in simulated body fluid for 1, 3, and 7 days. The surface microstructures and chemical property changes after soaking in simulated body fluid were again characterized by field emission scanning electron microscope, energy-dispersive X-ray spectrometer, and Fourier transform infrared spectroscopy. Results of this study demonstrated that the functional -PO4 groups introduced onto the PAA surface dramatically promoted the deposition of bone-like apatite on PAA. The results from this study indicated that the phosphorylation treatment of anodic alumina is an effective method for inducing bone-like apatite formation, and this phosphorylated PAA can be a promising candidate to be used as bioactive surface coatings on implant metals and alloys for orthopedic and dental applications. PMID:24598060

  8. Synthetic apatite nanoparticles as a phosphorus fertilizer for soybean (Glycine max).

    PubMed

    Liu, Ruiqiang; Lal, Rattan

    2014-01-01

    Some soluble phosphate salts, heavily used in agriculture as highly effective phosphorus (P) fertilizers, cause surface water eutrophication, while solid phosphates are less effective in supplying the nutrient P. In contrast, synthetic apatite nanoparticles could hypothetically supply sufficient P nutrients to crops but with less mobility in the environment and with less bioavailable P to algae in comparison to the soluble counterparts. Thus, a greenhouse experiment was conducted to assess the fertilizing effect of synthetic apatite nanoparticles on soybean (Glycine max). The particles, prepared using one-step wet chemical method, were spherical in shape with diameters of 15.8 ± 7.4 nm and the chemical composition was pure hydroxyapatite. The data show that application of the nanoparticles increased the growth rate and seed yield by 32.6% and 20.4%, respectively, compared to those of soybeans treated with a regular P fertilizer (Ca(H2PO4)2). Biomass productions were enhanced by 18.2% (above-ground) and 41.2% (below-ground). Using apatite nanoparticles as a new class of P fertilizer can potentially enhance agronomical yield and reduce risks of water eutrophication. PMID:25023201

  9. Bone-like apatite coating on functionalized poly(etheretherketone) surface via tailored silanization layers technique.

    PubMed

    Zheng, Yanyan; Xiong, Chengdong; Zhang, Shenglan; Li, Xiaoyu; Zhang, Lifang

    2015-10-01

    Poly(etheretherketone) (PEEK) is a rigid semi-crystalline polymer with outstanding mechanical properties, bone-like stiffness and suitable biocompatibility that has attracted much interest as a biomaterial for orthopedic and dental implants. However, the bio-inert surface of PEEK limits its biomedical applications when direct osteointegration between the implants and the host tissue is desired. In this work, -PO4H2, -COOH and -OH groups were introduced on the PEEK surface by further chemical treatments of the vinyl-terminated silanization layers formed on the hydroxylation-pretreated PEEK surface. Both the surface-functionalized and pristine specimens were characterized by X-ray photoelectron spectroscopy (XPS), attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy and water contact angle measurements. When placed in 1.5 strength simulated body fluid (SBF) solution, apatite was observed to form uniformly on the functionalized PEEK surface and firmly attach to the substrate. The characterized results demonstrated that the coating was constituted by poorly crystallized bone-like apatite and the effect of surface functional groups on coating formation was also discussed in detail. In addition, in vitro biocompatibility of PEEK, in terms of pre-osteoblast cell (MC3T3-E1) attachment, spreading and proliferation, was remarkably enhanced by the bone-like apatite coating. Thus, this study provides a method to enhance the bioactivity of PEEK and expand its applications in orthopedic and dental implants. PMID:26117784

  10. Composition Determination and Cathodoluminescence of Natural Apatite from Different Phosphate Deposits in Northern China

    NASA Astrophysics Data System (ADS)

    Guo, Qingfeng; Liao, Libing; Xia, Zhiguo; Liu, Haikun

    2014-06-01

    Two kinds of natural apatite minerals were obtained from two different phosphate deposits in northern China, FanShan, Hebei province and HeiYingShan, Inner Mongolia province. Their chemical compositions, phase structure, and cathodoluminescence (CL) have been comparatively investigated. X-ray diffraction (XRD) analysis indicated that the raw phosphate minerals from FanShan mainly are composed of FanShan apatite (FA) and FanShan mica, respectively, while the ore sample from HeiYingShan contained HeiYingshan apatite (HA) and HeiYingshan magnetite. The mineralogical characteristics and crystal structure of FA and HA were further determined by XRD, scanning electron microscopy, x-ray fluorescence spectrometer, and inductively coupled plasma-mass spectrometry, respectively. These results indicate that FA belongs to fluorapatite, while the HA belongs to hydroxyapatite. The existence of some trace elements has also been verified by the measured CL spectrum. The origin of the observed CL peaks has been discussed, and the relationship of the CL and the chemical composition has also been investigated.

  11. Biomimetic Deposition of Apatite on Surface Chemically Modified Porous NiTi Shapememory Alloy

    NASA Astrophysics Data System (ADS)

    Wu, S. L.; Liu, X. M.; Chung, C. Y.; Chu, Paul K.; Chan, Y. L.; Yeung, K. W. K.; Chu, C. L.

    Porous NiTi shape memory alloy (SMA) with 48% porosity and an average pore size of 50-800 μm was synthesized by capsule-free hot isostatic pressing (CF-HIP). To enhance the surface bioactivity, the porous NiTi SMA was subjected to H2O2 and subsequent NaOH treatment. Scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy analyses revealed that a porous sodium titanate (Na2TiO3) film had formed on the surface of the porous NiTi SMA. An apatite layer was deposited on this film after immersion in simulated body fluid at 37°C, while no apatite could be found on the surface of the untreated porous NiTi SMA. The formation of the apatite layer infers that the bioactivity of the porous NiTi SMA may be enhanced by surface chemical treatment, which is favorable for its application as bone implants.

  12. Fission-track dating of apatite and zircon: An interlaboratory comparison

    USGS Publications Warehouse

    Naeser, C.W.; Zimmermann, R.A.; Cebula, G.T.

    1981-01-01

    Apatite and zircon separates from the Fish Canyon Tuff (K-Ar age, 27.9??0.7 Myr), San Juan Mtns., Colorado, have been given to over 50 laboratories for fission-track dating. Nineteen laboratories have reported fission-track ages that they have determined for apatites. Nine laboratories have reported their analysis of the zircons. The principal difference between the results reported by the laboratories reflects their choice of the decay constant. The laboratories which use a value of ??f ??? 7.0 ?? 10-17 yr-1 for the spontaneous-fission decay constant of 238U, report an average age for the apatite of 28.5??0.7 Myr, and those using ??f ??? = 8.4 ?? 10-17 yr-1 report an average age of 23.6??1.0 Myr. The average fission-track age for the zircons is 28.4??0.7 Myr. Only laboratories which use ??f ??? 7.0 ?? 10-17 yr-1 reported zircon data. ?? 1981.

  13. Synthetic apatite nanoparticles as a phosphorus fertilizer for soybean (Glycine max)

    NASA Astrophysics Data System (ADS)

    Liu, Ruiqiang; Lal, Rattan

    2014-07-01

    Some soluble phosphate salts, heavily used in agriculture as highly effective phosphorus (P) fertilizers, cause surface water eutrophication, while solid phosphates are less effective in supplying the nutrient P. In contrast, synthetic apatite nanoparticles could hypothetically supply sufficient P nutrients to crops but with less mobility in the environment and with less bioavailable P to algae in comparison to the soluble counterparts. Thus, a greenhouse experiment was conducted to assess the fertilizing effect of synthetic apatite nanoparticles on soybean (Glycine max). The particles, prepared using one-step wet chemical method, were spherical in shape with diameters of 15.8 +/- 7.4 nm and the chemical composition was pure hydroxyapatite. The data show that application of the nanoparticles increased the growth rate and seed yield by 32.6% and 20.4%, respectively, compared to those of soybeans treated with a regular P fertilizer (Ca(H2PO4)2). Biomass productions were enhanced by 18.2% (above-ground) and 41.2% (below-ground). Using apatite nanoparticles as a new class of P fertilizer can potentially enhance agronomical yield and reduce risks of water eutrophication.

  14. In vivo bioactivity of titanium and fluorinated apatite coatings for orthopaedic implants: a vibrational study

    NASA Astrophysics Data System (ADS)

    Taddei, Paola; Tinti, Anna; Reggiani, Matteo; Monti, Patrizia; Fagnano, Concezio

    2003-06-01

    The bone integration of implants is a complex process which depends on chemical composition and surface morphology. To accelerate osteointegration, metal implants are coated with porous metal or apatites which have been reported to increase mineralisation, improving prosthesis fixation. To study the influence of composition and morphology on the in vivo bioactivity, titanium screws coated by Plasma Flame Spraying (PFS) with titanium or fluorinated apatite (K690) were implanted in sheep tibia and femur for 10 weeks and studied by micro-Raman and IR spectroscopy. The same techniques, together with thermogravimetry, were used for characterising the pre-coating K690 powder. Contrary to the manufacturer report, the K690 pre-coating revealed to be composed of a partially fluorinated apatite containing impurities of Ca(OH) 2 and CaCO 3. By effect of PFS, the impurities were decomposed and the crystallinity degree of the coating was found to decrease. The vibrational spectra recorded on the implanted screws revealed the presence of newly formed bone; for the K690-coated screws at least, a high level of osteointegration was evidenced.

  15. Failure of a Glass Ionomer to Remineralize Apatite-depleted Dentin

    PubMed Central

    Kim, Y.K.; Yiu, C.K.Y.; Kim, J.R.; Gu, L.; Kim, S.K.; Weller, R.N.; Pashley, D.H.; Tay, F.R.

    2010-01-01

    Remineralization of demineralized dentin lesions adjacent to glass-ionomer cements (GICs) has been reported in the literature. This study tested the hypothesis that a strontium-based GIC can remineralize completely demineralized dentin by nucleation of new apatite crystallites within an apatite-free dentin matrix. Human dentin specimens were acid-etched, bonded with Fuji IXGP, and immersed in a calcium-and-phosphate-containing 1.5X simulated body fluid (SBF) for 1-4 months. Polyacrylic acid and polyvinylphosphonic acid biomimetic analogs were added to the SBFs to create 2 additional remineralization media. Specimens were processed by transmission electron microscopy (TEM). No apatite deposition could be identified in the completely demineralized dentin in any of the specimens immersed in the 3 remineralization media, despite TEM/EDX evidence of diffusion of ions specific to the strontium-based GIC into the demineralized dentin. The hypothesis was rejected; mineral concentration alone is not a sufficient endpoint for assessing the success of contemporary remineralization strategies. PMID:20110510

  16. Long-term evaluation of the degradation behavior of three apatite-forming calcium phosphate cements.

    PubMed

    An, Jie; Liao, Hongbing; Kucko, Nathan W; Herber, Ralf-Peter; Wolke, Joop G C; van den Beucken, Jeroen J J P; Jansen, John A; Leeuwenburgh, Sander C G

    2016-05-01

    Calcium phosphate cements (CPCs) are injectable bone substitutes with a long clinical history because of their biocompatibility and osteoconductivity. Nevertheless, their cohesion upon injection into perfused bone defects as well as their long-term degradation behavior remain major clinical challenges. Therefore, the long-term degradation behavior of two types of α-tricalcium phosphate-based, apatite-forming CPCs was compared to a commercially available apatite-forming cement, that is HydroSet(TM) . Carboxyl methylcellulose (CMC) was used as cohesion promotor to improve handling properties of the two experimental cements, whereas poly (d, l-lactic-co-glycolic) acid (PLGA) microparticles were added to introduce macroporosity and stimulate CPC degradation. All three CPCs were injected into defects drilled into rabbit femoral condyles and explanted after 4, 12, or 26 weeks, after which the bone response was assessed both qualitatively and quantitatively. CPCs without PLGA microparticles degraded only at the periphery of the implants, while the residual CPC volume was close to 90%. On the contrary, bone ingrowth was observed not only at the periphery of the CPC, but also throughout the center of the implants after 26 weeks of implantation for the PLGA-containing CPCs with a residual CPC volume of approximately 55%. In conclusion, it was shown that CPC containing CMC and PLGA was able to induce partial degradation of apatite-forming CPCs and concomitant replacement by bone tissue. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 1072-1081, 2016. PMID:26743230

  17. Phosphorylation-dependent mineral-type specificity for apatite-binding peptide sequences.

    PubMed

    Addison, William N; Miller, Sharon J; Ramaswamy, Janani; Mansouri, Ahmad; Kohn, David H; McKee, Marc D

    2010-12-01

    Apatite-binding peptides discovered by phage display provide an alternative design method for creating functional biomaterials for bone and tooth tissue repair. A limitation of this approach is the absence of display peptide phosphorylation--a post-translational modification important to mineral-binding proteins. To refine the material specificity of a recently identified apatite-binding peptide, and to determine critical design parameters (net charge, charge distribution, amino acid sequence and composition) controlling peptide affinity for mineral, we investigated the effects of phosphorylation and sequence scrambling on peptide adsorption to four different apatites (bone-like mineral, and three types of apatite containing initially 0, 5.6 and 10.5% carbonate). Phosphorylation of the VTKHLNQISQSY peptide (VTK peptide) led to a 10-fold increase in peptide adsorption (compared to nonphosphorylated peptide) to bone-like mineral, and a 2-fold increase in adsorption to the carbonated apatite, but there was no effect of phosphorylation on peptide affinity to pure hydroxyapatite (without carbonate). Sequence scrambling of the nonphosphorylated VTK peptide enhanced its specificity for the bone-like mineral, but scrambled phosphorylated VTK peptide (pVTK) did not significantly alter mineral-binding suggesting that despite the importance of sequence order and/or charge distribution to mineral-binding, the enhanced binding after phosphorylation exceeds any further enhancement by altered sequence order. Osteoblast culture mineralization was dose-dependently inhibited by pVTK and to a significantly lesser extent by scrambled pVTK, while the nonphosphorylated and scrambled forms had no effect, indicating that inhibition of osteoblast mineralization is dependent on both peptide sequence and charge. Computational modeling of peptide-mineral interactions indicated a favorable change in binding energy upon phosphorylation that was unaffected by scrambling. In conclusion

  18. A taxonomy of apatite frameworks for the crystal chemical design of fuel cell electrolytes

    SciTech Connect

    Pramana, Stevin S.; Klooster, Wim T.; White, Timothy J.

    2008-08-15

    Apatite framework taxonomy succinctly rationalises the crystallographic modifications of this structural family as a function of chemical composition. Taking the neutral apatite [La{sub 8}Sr{sub 2}][(GeO{sub 4}){sub 6}]O{sub 2} as a prototype electrolyte, this classification scheme correctly predicted that 'excess' oxygen in La{sub 9}SrGe{sub 6}O{sub 26.5} is tenanted in the framework as [La{sub 9}Sr][(GeO{sub 4}){sub 5.5}(GeO{sub 5}){sub 0.5}]O{sub 2}, rather than the presumptive tunnel location of [La{sub 9}Sr][(GeO{sub 4}){sub 6}]O{sub 2.5}. The implication of this approach is that in addition to the three known apatite genera-A{sub 10}(BO{sub 3}){sub 6}X{sub 2}, A{sub 10}(BO{sub 4}){sub 6}X{sub 2}, A{sub 10}(BO{sub 5}){sub 6}X{sub 2}-hybrid electrolytes of the types A{sub 10}(BO{sub 3}/BO{sub 4}/BO{sub 5}){sub 6}X{sub 2} can be designed, with potentially superior low-temperature ion conduction, mediated by the introduction of oxygen to the framework reservoir. - Graphical abstract: Apatite framework taxonomy succinctly rationalises the crystallographic modifications of this structural family as a function of chemical composition. Neutron diffraction identified that the excess oxygen in La{sub 9}SrGe{sub 6}O{sub 26.5} is tenanted in the framework as [La{sub 9}Sr][(GeO{sub 4}){sub 5.5}(GeO{sub 5}){sub 0.5}]O{sub 2}. The implication of this approach is that in addition to the three known apatite genera-A{sub 10}(BO{sub 3}){sub 6}X{sub 2}, A{sub 10}(BO{sub 4}){sub 6}X{sub 2}, A{sub 10}(BO{sub 5}){sub 6}X{sub 2}-hybrid electrolytes of the types A{sub 10}(BO{sub 3}/BO{sub 4}/BO{sub 5}){sub 6}X{sub 2} can be designed.

  19. Phosphorylation-dependent mineral type specificity for apatite-binding peptide sequences

    PubMed Central

    Addison, William N.; Miller, Sharon J.; Ramaswamy, Janani; Mansouri, Ahmad; Kohn, David H.; McKee, Marc D.

    2010-01-01

    Apatite-binding peptides discovered by phage display provide an alternative design method for creating functional biomaterials for bone and tooth tissue repair. A limitation of this approach is the absence of display peptide phosphorylation – a post-translational modification important to mineral-binding proteins. To refine the material specificity of a recently identified apatite-binding peptide, and to determine critical design parameters (net charge, charge distribution, amino acid sequence and composition) controlling peptide affinity for mineral, we investigated the effects of phosphorylation and sequence scrambling on peptide adsorption to four different apatites (bone-like mineral, and three types of apatite containing initially 0, 5.6 and 10.5% carbonate). Phosphorylation of peptide VTKHLNQISQSY (pVTK) led to a 10-fold increase in peptide adsorption (compared to nonphosphorylated peptide) to bone-like mineral, and a 2-fold increase in adsorption to the carbonated apatite, but there was no effect of phosphorylation on peptide affinity to pure hydroxyapatite (without carbonate). Sequence scrambling of the nonphosphorylated VTK peptide enhanced its specificity for the bone-like mineral, but scrambled pVTK peptide did not significantly alter mineral-binding suggesting that despite the importance of sequence order and/or charge distribution to mineral binding, the enhanced binding after phosphorylation exceeds any further enhancement by altered sequence order. Osteoblast culture mineralization was dose-dependently inhibited by pVTK and to a significantly lesser extent by scrambled pVTK, while the nonphosphorylated and scrambled forms had no effect, indicating that inhibition of osteoblast mineralization is dependent on both peptide sequence and charge. Computational modeling of peptide-mineral interactions indicated a favorable change in binding energy upon phosphorylation that was unaffected by scrambling. In conclusion, phosphorylation of serine residues

  20. The kinetics of clumped-isotope reactions in calcite and apatite from natural and experimental samples

    NASA Astrophysics Data System (ADS)

    Stolper, D. A.; Eiler, J. M.

    2014-12-01

    Measurements of clumped isotopes of carbonate-bearing minerals are a powerful tool for reconstructing past surface temperatures and thermal histories of shallow crustal rocks. Because the clumped-isotope thermometer is based on homogenous-phase equilibrium, a sample's clumped-isotope temperature is susceptible to resetting through, for example, intracrystalline diffusion and redistribution of C and O isotopes during (re)heating or slow cooling. Quantitative knowledge of the kinetics of this resetting have received increasing attention (1-3) and is critical for understanding the meaning of clumped-isotope temperatures of samples with complex burial histories. To better constrain these kinetics and complement previous work (1-3) we performed heating experiments (400-700°C) on optical calcites and carbonate-bearing apatites. As previously observed (2-3), calcites exhibit non-first-order kinetics. The data were fit using a model that incorporates both diffusion and isotope-exchange reactions (4). The kinetics derived with this model using the optical-calcite heating experiments of (2) and those measured here are indistinguishable. The model predicts that subtle changes (>10°C) in measured calcite clumped-isotope temperatures can occur at burial temperatures between 60-100°C on million-year timescales. Though small, such changes may have an impact on clumped-isotope-based reconstructions of past surface temperatures and thermal histories. The derived kinetics were compared to clumped-isotope measurements of cogenetic calcites and apatites from slowly cooled carbonatite intrusions. Apparent temperatures are 70-140°C for apatites and 120-190°C for calcites. Measured temperatures for calcites match modeled temperatures using reasonable geological cooling rates. Natural apatite samples yield lower apparent temperatures than predicted based on the model. We propose that this difference is the result of annealment of structural damage in apatites (e.g., generated by

  1. Orientation Dependent Polarized Micro-XAS Study of U, Th and Sr in Single Crystal Apatites

    NASA Astrophysics Data System (ADS)

    Luo, Y.; Rakovan, J.; Wright, S.

    2009-05-01

    In order to evaluate apatite as a potential solid nuclear waste form and a contaminant sequestration agent, the complimentary use of single crystal X-ray diffraction and X-ray absorption spectroscopy (XAS) is applied to the study of U, Th, and Sr doped apatite single crystals to investigate the site preference, oxidation state, and structural distortions created by these substituents. Single crystal X-ray diffraction provides average information regarding the site occupancy of U and Th in apatites. Extended X-ray absorption fine-structure (EXAFS) yields quantitative information of the local structure of these substituents, which includes near-neighbor distances, coordination numbers and variations in bond distances; while X-ray absorption near edge structure (XANES) is used to determine the oxidation states of U. Restricted by the typical small size (20-100 μm) and volume of our synthetic samples, Micro-XAS is required. Different from studies which take full advantage of the polarization of synchrotron radiation, our Micro- XAS study on single crystal apatites was hampered by the polarization effects. In order to extract precise information of valence state and structural variation from XAS, it is necessary to know the crystallographic orientation of the sample with respect to the polarization direction of the incident X-ray beam during data collection. To do this we have designed and built a portable goniometer that duplicates the geometry of our laboratory standard Bruker Apex diffractometer goniometer. Crystal orientation is determined by X-ray diffraction at our home institution. The portable goniometer is then set up on the experimental table at synchrotron facilities and the crystal can be set in any specific known orientation. The lattice orientation determined by X-ray diffraction is applied to XAS data analysis, specifically calculation of scattering amplitudes and phase shifts, to account for polarization effects of synchrotron radiation. The goniometer

  2. Using Apatite to Model Chlorine Contents of High SiO2 Magmas: An Enhanced Methodological Approach

    NASA Astrophysics Data System (ADS)

    Flesch, R.; Webster, J. D.; Nadeau, P. A.

    2015-12-01

    Hydrothermal experiments were conducted on high-silica (73-75 wt% SiO2), fluid-saturated melts at 844-862°C and ca. 50 MPa using crushed glass of the Los Posos rhyolite. Water and salts including NaCl, KCl, Ca(OH)2, and CaHPO4 and HCl were added proportionally to the experiments to restrict the variability of the aluminosity of the melt. The Durango apatite, which contains 3.53 wt% F and 0.41% Cl, was added as "seeds"<5µm in diameter to stimulate apatite growth during the experiments. Samples were loaded into gold capsules and run in cold-seal pressure vessels for durations of 286-1008 hours. Temperature was cycled at ±20˚C to promote apatite crystallization. Electron microprobe analyses of run-product glasses and embedded apatite grains support calculation of a range of partition coefficients ( = wt% Cl in apatite/wt% Cl in melt) of 4.7 to 15.9. The mole fraction of Cl in experimental apatites, or XCl, ranges from 0.19 to 0.56, while XF ranges from 0.08 to 0.63. The computed values for XOH range from 0.24 to 0.38. We find that normalizing XCl to XOH of apatites dramatically improves the precision when using apatite compositions to model Cl contents of melts. We compare our Los Posos rhyolite experiments with published data on 50 MPa rhyodacite experiments and find that Cl partitioning is significantly different in each system. Given the importance of chlorine in fluid equilibria, ore transport, and magma evolution, applications of apatite as a proxy for Cl contents in melts are unbounded. It is found that in order to accurately use the volatile composition of natural and synthetic apatites to calculate the volatile composition of melts in felsic systems, several chemical factors, including wt% SiO2 and the aluminosity/alkalinity of melts, should be incorporated as parameters to enhance relevant modeling. This allows geochemists to place better constraints on processes associated with crystallizing Cl-bearing magmatic systems.

  3. CoQ10 deficiencies and MNGIE: Two Treatable Mitochondrial Disorders

    PubMed Central

    Hirano, Michio; Garone, Caterine; Quinzii, Catarina M.

    2012-01-01

    Background Although causative mutations have been identified for numerous mitochondrial disorders, few disease-modifying treatments are available. Two examples of treatable mitochondrial disorders are coenzyme Q10 (CoQ10 or ubiquinone) deficiency and mitochondrial neurogastrointestinal encephalomyopathy (MNGIE). Scope of Review Here, we describe clinical and molecular features of CoQ10 deficiencies and MNGIE and explain how understanding their pathomechanisms have led to rationale therapies. Primary CoQ10 deficiencies, due to mutations in genes required for ubiquinone biosynthesis, and secondary deficiencies, caused by genetic defects not directly related to CoQ10 biosynthesis, often improve with CoQ10 supplementation. In vitro and in vivo studies of CoQ10 deficiencies have revealed biochemical alterations that may account for phenotypic differences among patients and variable responses to therapy. In contrast to the heterogeneous CoQ10 deficiencies, MNGIE is a single autosomal recessive disease due to mutations in the TYMP gene encoding thymidine phosphorylase (TP). In MNGIE, loss of TP activity causes toxic accumulations of the nucleosides thymidine and deoxyuridine that are incorporated by the mitochondrial pyrimidine salvage pathway and cause deoxynucleoside triphosphate pool imbalances, which, in turn cause mtDNA instability. Allogeneic hematopoetic stem cell transplantation to restore TP activity and eliminate toxic metabolites is a promising therapy for MNGIE. Conclusions CoQ10 deficiencies and MNGIE demonstrate the feasibility of treating specific mitochondrial disorders through replacement of deficient metabolites or via elimination of excessive toxic molecules. General Significance Studies of CoQ10 deficiencies and MNGIE illustrate how understanding the pathogenic mechanisms of mitochondrial diseases can lead to meaningful therapies. PMID:22274133

  4. Savannah River Site chemical, metal, and pesticide (CMP) waste vitrification treatability studies

    SciTech Connect

    Cicero, C.A.

    1997-01-13

    Numerous Department of Energy (DOE) facilities, as well as Department of Defense (DOD) and commercial facilities, have used earthen pits for disposal of chemicals, organic contaminants, and other waste materials. Although this was an acceptable means of disposal in the past, direct disposal into earthen pits without liners or barriers is no longer a standard practice. At the Savannah River Site (SRS), approximately three million pounds of such material was removed from seven chemical, metal, and pesticide disposal pits. This material is known as the Chemical, Metal, and Pesticide (CMP) Pit waste and carries several different listed waste codes depending on the contaminants in the respective storage container. The waste is not classified as a mixed waste because it is believed to be non-radioactive; however, in order to treat the material in a non-radioactive facility, the waste would first have to be screened for radioactivity. The Defense Waste Processing Technology (DWPT) Section of the Savannah River Technology Center (SRTC) was requested by the DOE-Savannah River (SR) office to determine the viability of vitrification of the CMP Pit wastes. Radioactive vitrification facilities exist which would be able to process this waste, so the material would not have to be analyzed for radioactive content. Bench-scale treatability studies were performed by the DWPT to determine whether a homogeneous and durable glass could be produced from the CMP Pit wastes. Homogeneous and durable glasses were produced from the six pits sampled. The optimum composition was determined to be 68.5 wt% CMP waste, 7.2 wt% Na{sub 2}O, 9 wt% CaO, 7.2 wt% Li{sub 2}O and 8.1 wt% Fe{sub 2}O{sub 3}. This glass melted at 1,150 C and represented a two fold volume reduction.

  5. Induction Tempering vs Conventional Tempering of a Heat-Treatable Steel

    NASA Astrophysics Data System (ADS)

    Sackl, Stephanie; Zuber, Michael; Clemens, Helmut; Primig, Sophie

    2016-05-01

    An induction heat treatment is favorable compared to a conventional one mainly due to significant time and cost savings. Therefore, in this study, the microstructure property relationships during induction and conventional heat treatment of a heat treatable steel 42CrMo4 is investigated. The yield strength and hardness is slightly higher for the conventionally heat-treated steel, whereas the induction heat-treated condition exhibits a roughly 30 J/cm2 higher impact energy. In a previous investigation of the authors, it has been proved that the difference in yield strength originates from the smaller block size of the conventionally heat-treated steel, which was already present after hardening. In the present work, it can be shown that during tempering the martensitic blocks become equi-axed ferrite grains due to recrystallization as revealed by electron back scatter diffraction. Nevertheless, a larger grain size usually is less favorable for the impact toughness of steels. Therefore, another mechanism is responsible for the higher impact energy of the induction hardened and tempered steel. With the aid of transmission electron microscopy a finer distribution of cementite was observed in the induction heat-treated samples. The delay of recovery is the reason for the presence of finer cementite in case of the induction heat-treated steel. Here, the higher heating rates and shorter process times reduce the annihilation of dislocation and as a consequence provide more nucleation sites for precipitation of cementite during tempering. From the obtained experimental results, it is believed that the finer distribution of carbides causes the observed higher impact toughness.

  6. Induction Tempering vs Conventional Tempering of a Heat-Treatable Steel

    NASA Astrophysics Data System (ADS)

    Sackl, Stephanie; Zuber, Michael; Clemens, Helmut; Primig, Sophie

    2016-07-01

    An induction heat treatment is favorable compared to a conventional one mainly due to significant time and cost savings. Therefore, in this study, the microstructure property relationships during induction and conventional heat treatment of a heat treatable steel 42CrMo4 is investigated. The yield strength and hardness is slightly higher for the conventionally heat-treated steel, whereas the induction heat-treated condition exhibits a roughly 30 J/cm2 higher impact energy. In a previous investigation of the authors, it has been proved that the difference in yield strength originates from the smaller block size of the conventionally heat-treated steel, which was already present after hardening. In the present work, it can be shown that during tempering the martensitic blocks become equi-axed ferrite grains due to recrystallization as revealed by electron back scatter diffraction. Nevertheless, a larger grain size usually is less favorable for the impact toughness of steels. Therefore, another mechanism is responsible for the higher impact energy of the induction hardened and tempered steel. With the aid of transmission electron microscopy a finer distribution of cementite was observed in the induction heat-treated samples. The delay of recovery is the reason for the presence of finer cementite in case of the induction heat-treated steel. Here, the higher heating rates and shorter process times reduce the annihilation of dislocation and as a consequence provide more nucleation sites for precipitation of cementite during tempering. From the obtained experimental results, it is believed that the finer distribution of carbides causes the observed higher impact toughness.

  7. Mortality from treatable illnesses in marginally housed adults: a prospective cohort study

    PubMed Central

    Jones, Andrea A; Vila-Rodriguez, Fidel; Leonova, Olga; Langheimer, Verena; Lang, Donna J; Barr, Alasdair M; Procyshyn, Ric M; Smith, Geoffrey N; Schultz, Krista; Buchanan, Tari; Krausz, Michael; Montaner, Julio S; MacEwan, G William; Rauscher, Alexander; Panenka, William J; Thornton, Allen E; Honer, William G

    2015-01-01

    Objectives Socially disadvantaged people experience greater risk for illnesses that may contribute to premature death. This study aimed to evaluate the impact of treatable illnesses on mortality among adults living in precarious housing. Design A prospective cohort based in a community sample. Setting A socially disadvantaged neighbourhood in Vancouver, Canada. Participants Adults (N=371) living in single room occupancy hotels or recruited from the Downtown Community Court and followed for median 3.8 years. Main outcome measures Participants were assessed for physical and mental illnesses for which treatment is currently available. We compared cohort mortality rates with 2009 Canadian rates. Left-truncated Cox proportional hazards modelling with age as the time scale was used to assess risk factors for earlier mortality. Results During 1269 person-years of observation, 31/371 (8%) of participants died. Compared with age-matched and sex-matched Canadians, the standardised mortality ratio was 8.29 (95% CI 5.83 to 11.79). Compared with those that had cleared the virus, active hepatitis C infection was a significant predictor for hepatic fibrosis adjusting for alcohol dependence and age (OR=2.96, CI 1.37 to 7.08). Among participants <55 years of age, psychosis (HR=8.12, CI 1.55 to 42.47) and hepatic fibrosis (HR=13.01, CI 3.56 to 47.57) were associated with earlier mortality. Treatment rates for these illnesses were low (psychosis: 32%, hepatitis C virus: 0%) compared with other common disorders (HIV: 57%, opioid dependence: 61%) in this population. Conclusions Hepatic fibrosis and psychosis are associated with increased mortality in people living in marginal conditions. Timely diagnosis and intervention could reduce the high mortality in marginalised inner city populations. PMID:26297373

  8. Pilot-scale treatability test plan for the 100-HR-3 operable unit

    SciTech Connect

    Not Available

    1994-08-01

    This document presents the treatability test plan for pilot-scale pump-and-treat testing at the 100-HR-3 Operable Unit. The test will be conducted in fulfillment of interim Milestone M-15-06E to begin pilot-scale pump-and-treat operations by August 1994. The scope of the test was determined based on the results of lab/bench-scale tests (WHC 1993a) conducted in fulfillment of Milestone M-15-06B. These milestones were established per agreement between the U.S. Department of Energy (DOE), the Washington State Department of Ecology and the U.S. Environmental Protection Agency (EPA), and documented on Hanford Federal of Ecology Facility Agreement and Consent Order Change Control Form M-15-93-02. This test plan discusses a pilot-scale pump-and-treat test for the chromium plume associated with the D Reactor portion of the 100-HR-3 Operable Unit. Data will be collected during the pilot test to assess the effectiveness, operating parameters, and resource needs of the ion exchange (IX) pump-and-treat system. The test will provide information to assess the ability to remove contaminants by extracting groundwater from wells and treating extracted groundwater using IX. Bench-scale tests were conducted previously in which chromium VI was identified as the primary contaminant of concern in the 100-D reactor plume. The DOWEX 21K{trademark} resin was recommended for pilot-scale testing of an IX pump-and-treat system. The bench-scale test demonstrated that the system could remove chromium VI from groundwater to concentrations less than 50 ppb. The test also identified process parameters to monitor during pilot-scale testing. Water will be re-injected into the plume using wells outside the zone of influence and upgradient of the extraction well.

  9. Molasses enhanced phyto and bioremediation treatability study of explosives contaminated Hawaiian soils.

    PubMed

    Lamichhane, Krishna M; Babcock, Roger W; Turnbull, Steve J; Schenck, Susan

    2012-12-01

    A 15-week treatability study was conducted in a greenhouse to evaluate the potential effects of molasses on the bioremediation and phytoremediation potential of Guinea Grass (Panicum maximum) for treating energetic contaminated soil from the open burn/open detonation area of the Makua Military Reservation, Oahu, HI (USA). The energetics in the soil were royal demolition explosive (RDX) and high-melting explosive (HMX). Among the 6 treatments employed in this study, enhanced removal of RDX was observed from treatments that received molasses and went to completion. The RDX degradation rates in treatments with molasses diluted 1:20 and 1:40 were comparable suggesting that the lower dose worked as well as the higher dose. Treatments without molasses degraded RDX slowly and residuals remained after 15 weeks. The bacterial densities in molasses-treated units were much greater than those without molasses. Phytoremediation alone seems to have little effect on RDX disappearance. For HMX, neither bioremediation nor phytoremediation was found to be useful in reducing the concentration within the experimental period. The concentrations of nitrogen and phosphorous in the soil did not change significantly during the experiment, however, a slight increase in soil pH was observed in all treatments. The study showed that irrigating with diluted molasses is effective at enhancing RDX degradation mainly in the root zone and just below it. The long term sustainability of active training ranges can be enhanced by bioremediation using molasses treatments to prevent RDX deposited by on-going operations from migrating through the soil to groundwater and off-site. PMID:23164624

  10. Anaerobic treatability of liquid residue from wet oxidation of sewage sludge.

    PubMed

    Bertanza, Giorgio; Galessi, Raniero; Menoni, Laura; Pedrazzani, Roberta; Salvetti, Roberta; Zanaboni, Sabrina

    2015-05-01

    Wet Oxidation (WO) of sewage sludge is a chemical oxidation of sludge at high temperatures and pressures by means of an oxygen-containing gas. The liquid stream originated by WO is easily biodegradable, and therefore, the recirculation to the biological Waste Water Treatment Plant (WWTP) may be a feasible solution. However, the WO effluent has a residual organic and nitrogen content so that its treatment may be required when the receiving WWTP has no surplus treatment capacity left. The aim of this research was the assessment of the anaerobic treatability of the WO liquid residue, in order to reduce the organic load to be recirculated to the WWTP, simultaneously promoting energy recovery. For this purpose, the liquid residue obtained during full scale WO tests on two different types of sludge was submitted to anaerobic digestion in a continuous flow pilot reactor (V = 5 L). Furthermore, batch tests were carried out in order to evaluate possible inhibition factors. Experimental results showed that, after the start-up/acclimation period (~130 days), Chemical Oxygen Demand (COD) removal efficiency was stably around 60% for about 120 days, despite the change in operating conditions. In the last phase of the experimental activity, COD removal reached 70% under the following treatment conditions: Hydraulic Retention Time (HRT) = 20 days, Volumetric Organic Loading Rate (VOLR) = 0.868 kg COD/m(3)/day, Organic Loading Rate per Volatile Suspended Solids (OLRvss) = 0.078 kg COD/kg VSS/day, temperature (T) = 36.5 °C, pH = 8. Energy balance calculation demonstrated anaerobic treatment sustainability. PMID:25035054

  11. Biological Apatite Formed from Polyphosphate and Alkaline Phosphatase May Exchange Oxygen Isotopes from Water through Carbonate

    NASA Astrophysics Data System (ADS)

    Omelon, S. J.; Stanley, S. Y.; Gorelikov, I.; Matsuura, N.

    2011-12-01

    The oxygen isotopic composition in bone mineral phosphate is known to reflect the local water composition, environmental humidity, and diet1. Once ingested, biochemical processes presumably equilibrate PO43- with "body water" by the many biochemical reactions involving PO43- 2. Blake et al. demonstrated that enzymatic release of PO43- from organophosphorus compounds, and microbial metabolism of dissolved orthophosphate, significantly exchange the oxygen in precipitated apatite within environmental water3,4, which otherwise does not exchange with water at low temperatures. One of the enzymes that can cleave phosphates from organic substrates is alkaline phosphastase5, the enzyme also associated with bone mineralization. The literature often states that the mineral in bone in hydroxylapatite, however the mineral in bone is carbonated apatite that also contains some fluoride6. Deprotonation of HPO32- occurs at pH 12, which is impossibly high for biological system, and the predominate carbonate species in solution at neutral pH is HCO3-. To produce an apatite mineral without a significant hydroxyl content, it is possible that apatite biomineralization occurs through a polyphosphate pathway, where the oxygen atom required to transform polyphosphate into individual phosphate ions is from carbonate: [PO3-]n + CO32- -> [PO3-]n-1 + PO43- + CO2. Alkaline phosphatase can depolymerise polyphosphate into orthophosphate5. If alkaline phosphatase cleaves an oxygen atom from a calcium-carbonate complex, then there is no requirement for removing a hydrogen atom from the HCO3- or HPO43- ions of body water to form bioapatite. A mix of 1 mL of 1 M calcium polyphosphate hydogel, or nano-particles of calcium polyphosphate, and amorphous calcium carbonate were reacted with alkaline phosphatase, and maintained at neutral to basic pH. After two weeks, carbonated apatite and other calcium phosphate minerals were identified by powder x-ray diffraction. Orthophosphate and unreacted

  12. Combining apatite fission track and He thermochronology to constrain thermal histories

    NASA Astrophysics Data System (ADS)

    Persano, C.; Stuart, F.; Bishop, P.

    2003-04-01

    Apatite fission track thermochronometry (AFTT) has proved an invaluable tool for determining the cooling histories of rocks in the shallow crust. Quantitative models for the time and temperature dependence of the fission track annealing process in apatite demostrate that the combination of fission track apparent age and track length distribution provides a continuous record of the thermal history of the samples from 120 to 60^oC, and possibly, to lower temperatures. However the sensitivity of the technique is poorly constrained below 70-80^oC because annealing rates are slow. The apatite (U-Th)/He system is sensitive to temperatures between 80 and 40^oC irrespective of apatite chemistry, and presents a way to test the ability of AFTT to determine thermal histories below 80^oC. Here we present a novel way of combining apatite fission track and (U-Th)/He data that narrows the number of possible thermal histories and provides better constraints on the landscape evolution of a particular region. We use as an example the southeastern Australia passive margin in NSW, an area where post break-up landscape evolution is poorly resolved despite an extensive fission track database. Fission track and (U-Th)/He ages have been measured on 16 apatite samples from two coast perpendicular traverses across the coastal plain, up the escarpment onto the plateau. The fission track data are modelled using AFTSolve and the individual thermal histories which fit the data are used as parameters for forward modelling the apatite He ages. Only the thermal histories that produce the measured He age, within uncertainty, are considered. For each sample, the choosen time-temperature paths show the same peculiar characteristics, narrowing considerably the number of possible cooling scenarios. This combination shows that the AFT/derived thermal histories for temperatures between 60 to 40^oC may be inconsistent with the (U-Th)/He ages, suggesting that the annealing process at this temperatures

  13. Ion microprobe U-Pb dating and strontium isotope analysis of biogenic apatite

    NASA Astrophysics Data System (ADS)

    Sano, Y.; Toyoshima, K.; Takahata, N.; Shirai, K.

    2012-12-01

    Conodonts are micro-fossils chemically composed of apatite which occurred in the body of one animal. They are guide fossils to show formation ages of sedimentary sequences with the highest resolution [1] and good samples to verify the dating method. We developed the ion microprobe U-Pb dating of apatite [2] and applied the method to a Carboniferous conodont [3] by using a SHRIMP II installed at Department of Earth and Planetary Sciences, Hiroshima University. Recently we have developed the NanoSIMS U-Pb dating method and successfully measured the formation ages of monazite [4] and zircon [5] at Atmosphere and Ocean Research Institute, University of Tokyo. In this work we carried out the NanoSIMS U-Pb dating of biogenic apatite such as conodont. Since the spot size of NanoSIMS is smaller than SHRIMP II, it is easier to have multi-spots on the single fragment of biogenic apatite. Based on the isochron method of U-Pb system, we have calculated the formation ages. They are consistent with those in literature. In order to study the chemical evolution of ocean during the past 600 Million years, strontium isotopes (87Sr/86Sr) of fossil marine carbonate such as coral skeletons and foraminifera tests were measured and compiled [6]. However they are not robust when the age is older than 500Ma, partly due to post-depositional histories. Apatite is more stable and more resistant to the alteration than carbonate [7]. Recently we have developed the method of NanoSIMS strontium isotopic analysis of a fish otolith, which composed of aragonite [8]. In this work we carried out the strontium isotopic analysis of biogenic apatite. The advantage of the ion microprobe technique over the TIMS (thermal ionization mass spectrometer) and MC-ICP-MS (multi-collector inductively coupled argon plasma mass spectrometer) method is preservation of the important textural context and to provide an opportunity for other simultaneous analytical work with high spatial resolution. This is the case for

  14. Treatable high homocysteine alone or in concert with five other thrombophilias in 1014 patients with thrombotic events.

    PubMed

    Glueck, Charles J; Smith, Domonique; Gandhi, Niral; Hemachandra, Kailash; Shah, Parth; Wang, Ping

    2015-10-01

    In 1014 patients with thrombotic events, we determined how often treatable high serum homocysteine alone, or in concert with five other thrombophilias, was associated with thrombotic events. We studied 1014 outpatients sequentially referred for evaluation of thrombotic events, all having six measures of thrombophilia--three PCR (methylenetetrahydrofolate reductase C677T-A1298C, factor V Leiden G506A, prothrombin G20210A), and three serologic (factors VIII, XI, homocysteine). Of the 1014 patients, 198 (20%) had atherothrombosis, 199 (20%) ocular vascular thrombosis, 211 (21%) osteonecrosis, 180 (18%) pseudotumor cerebri, and 123 (12%) recurrent miscarriage. In 434 of 1014 (43%) patients, all six thrombophilic measures were normal. High homocysteine, present in 126 of 1014 patients (12.4%), was the sole thrombophilia in 50 (5%), accompanied only by methylenetetrahydrofolate reductase homozygosity-compound heterozygosity in 22 (2.2%), and accompanied by other thrombophilias in 54 (5%). Patients were more likely than 110 healthy controls to have high homocysteine (12 vs. 5%; P = 0.02) and high factor VIII (21 vs. 7%; P = 0.0003). On treatment for a median of 18 months with L-methyl folate (5 mg), vitamin B6 (100 mg), and vitamin B12 (2 mg/day), in 74 homocysteinemic patients, median homocysteine fell from 15.6 to 10.0 μmol/l (P < 0.0001), and in 56 (76%), homocysteine fell to normal on treatment. When homocysteinemia was the sole thrombophilia, normalization of homocysteine was accompanied by freedom from new thrombotic events in 38 of 41 patients (93%). In evaluation of 1014 patients with thrombotic events, 126 (12%) had treatable high serum homocysteine, and in 50 (5%), high homocysteine was the sole treatable thrombophilia. PMID:25699608

  15. Laboratory treatability studies preparatory to field testing a resting-cell in situ microbial filter bioremediation strategy

    SciTech Connect

    Taylor, R.T.; Hanna, M.L.

    1995-04-01

    Prior to a down-hole-column treatability test of a Methylosinus trichosporium OB3b attached-resting-cell in situ biofilter strategy, a set of three sequential laboratory experiments were carried out to define several key operational parameters and to evaluate the likely degree of success at a NASA Kennedy Space Center site. They involved the cell attachment to site-specific sediments, the intrinsic resting-cell biotransformation capacities for the contaminants of interest plus their time-dependent extents of biodegradative removal at the concentrations of concern, and a scaled in situ mini-flow-through-column system that closely mimics the subsurface conditions during a field-treatability or pilot test of an emplaced resting-cell filter. These experiments established the conditions required for the complete metabolic removal of a vinyl chloride (VC), cis-dichlororthylene (cis-DCE) and trichloroethylene (TCE) mixture. However, the gas chromatographic (GC) procedures that we utilized and the mini-flow-through column data demonstrated that, at most, only about 50--70% of the site-water VC, cis-DCE, and TCE would be biodegraded. This occurred because of a limiting level of dissolved oxygen, which was exacerbated by the simultaneous presence of several additional previously unrecognized groundwater components, especially methane, that are also competing substrates for the whole-cell soluble methane monooxygenase (sMMO) enzyme complex. Irrespective, collectively the simplicity of the methods that we have developed and the results obtainable with them appear to provide relevant laboratory-based test-criteria before taking our microbial filter strategy to an in situ field treatability or pilot demonstration stage at other sites in the future.

  16. Inter- and intra-crystal REE variations in apatite from the Bob Ingersoll pegmatite, Black Hills, South Dakota

    SciTech Connect

    Jolliff, B.L.; Papike, J.J.; Shearer, C.K. ); Shimizu, N. )

    1989-02-01

    Concentrations of rare earth elements (REE) have been measured on a suite of apatite crystals from an internally zoned granitic pegmatite enriched in Li, B, Be, F, Nb, Ta, Sn and U with a Cameca IMS 3f ion microprobe using energy filtering. An apatite specimen from the Tin Mountain pegmatite, analyzed previously by isotope dilution, was used as a standard. The chondrite-normalized pattern determined with the ion microprobe closely matches the pattern determined by isotope dilution, with maxima at Sm and Dy, and minima at Nd and Er. Apatite samples from the Bob Ingersoll pegmatite show a large range of REE patterns and concentrations. In one case, apatite crystals within millimeters show differences in REE concentrations and pattern shapes, including a switch from positive to negative Eu anomalies. These effects may be coupled with non-ideal partitioning of REE in a heterogeneous mixture of melt, aqueous fluid and crystals. REE concentrations in apatite samples from the different pegmatite zones indicate a large variation in outer zones, high concentrations near the pegmatite core, and very low concentration in the core. Patterns are flat to slightly inclined (Ce/Yb: 1 to 5), and most samples have positive Eu anomalies. The magnitude of positive Eu anomalies decreases with inward position in the pegmatite, possibly indicating a progressive increase in {line integral}O{sub 2}, and a sharp increase may be indicated by systematic Ce depletion in apatite from the pegmatite core. REE-specific volatile complexes may contribute to variations, including unusual kinks, observed in REE patterns of apatite from mineral assemblages in upper parts of the pegmatite.

  17. The tetrad effect and geochemistry of apatite from the Altay Koktokay No. 3 pegmatite, Xinjiang, China: implications for pegmatite petrogenesis

    NASA Astrophysics Data System (ADS)

    Cao, Ming-Jian; Zhou, Qi-Feng; Qin, Ke-Zhang; Tang, Dong-Mei; Evans, Noreen J.

    2013-12-01

    In order to better constrain the evolution and petrogenesis of pegmatite, geochemical analysis was conducted on a suite of apatite crystals from the Altay Koktokay No. 3 pegmatite, Xinjiang, China and from the granitic and amphibolitic wall rocks. Apatite samples derived from pegmatite zones show convex tetrad effects in their REE patterns, extremely negative Eu anomalies and non-chondritic Y/Ho ratios. In contrast, chondritic Y/Ho ratios and convex tetrad effects are observed in the muscovite granite suggesting that different processes caused non-chondritic Y/Ho ratios and lanthanide tetrad effects. Based on the occurrence of convex tetrad effects in the host rocks and their associated minerals, we propose that the tetrad effects are likely produced from immiscible fluoride and silicate melts. This is in contrast to previous explanations of the tetrad effect; i.e. surface weathering, fractional crystallization and/or fluid-rock interaction. Additionally, we put forward that extreme negative Eu and non-chondritic Y/Ho in apatite are likely caused by the large amount of hydrothermal fluid exsolved from the pegmatite melts. Evolution of melt composition was found to be the primary cause of inter and intra-crystal major and trace element variations in apatite. Mn entering into apatite via substitution of Ca is supported by the positive correlation between CaO and MnO. Different evolution trends in apatite composition imply different crystallization environments between wall rocks and pegmatite zones. Based on the geochemistry of apatite samples, it is likely that there is a genetic relationship between the source of muscovite granite and the source of the pegmatite.

  18. Hydrothermal synthesis, structure investigation, and oxide ion conductivity of mixed Si/Ge-based apatite-type phases.

    PubMed

    Li, Henan; Baikie, Tom; Pramana, Stevin S; Shin, J Felix; Keenan, Philip J; Slater, Peter R; Brink, Frank; Hester, James; An, Tao; White, Tim J

    2014-05-19

    Apatite-type oxides ([A(I)4][A(II)6][(BO4)6]O2), particularly those of the rare-earth silicate and germanate systems, are among the more promising materials being considered as alternative solid oxide fuel cell electrolytes. Nonstoichiometric lanthanum silicate and germanate apatites display pure ionic conductivities exceeding those of yttria-stabilized zirconia at moderate temperatures (500-700 °C). In this study, mixed Si/Ge-based apatites were prepared by hydrothermal synthesis under mild conditions rather than the conventional solid-state method at high temperatures. Single-phase and highly crystalline nanosized apatite powders were obtained with the morphology changing across the series from spheres for the Si-based end member to hexagonal rods for the Ge-based end member. Powder X-ray and neutron analysis found all of these apatites to be hexagonal (P63/m). Quantitative X-ray microanalysis established the partial (<15 at%) substitution of La(3+) by Na(+) (introduced from the NaOH hydrothermal reagent), which showed a slight preference to enter the A(I) 4f framework position over the A(II) 6h tunnel site. Moreover, retention of hydroxide (OH(-)) was confirmed by IR spectroscopy and thermogravimetric analysis, and these apatites are best described as oxyhydroxyapatites. To prepare dense pellets for conductivity measurements, both conventional heat treatment and spark plasma sintering methods were compared, with the peculiar features of hydrothermally synthesized apatites and the influence of sodium on the ionic conductivity considered. PMID:24787953

  19. Facile preparation of apatite-type lanthanum silicate by a new water-based sol–gel process

    SciTech Connect

    Yamagata, Chieko; Elias, Daniel R.; Paiva, Mayara R.S.; Misso, Agatha M.; Castanho, Sonia R.H. Mello

    2013-06-01

    Highlights: ► We use a Na{sub 2}SiO{sub 3} waste solution as source of Si. ► We present a simple, rapid and low temperature method of lanthanum silicate apatite preparation. ► TEOS, a high cost reagent, was successfully substituted by a cheap price Na{sub 2}SiO{sub 3}, to obtain pure La{sub 9.56}(SiO{sub 4})6O{sub 2.33} lanthanum silicate apatite. - Abstract: In recent years, apatite-type lanthanum silicates ([Ln{sub 10−x}(XO{sub 4})6O{sub 3–1.5x}] (X = Si or Ge)) have been studied for use in SOFC (solid oxide fuel cells), at low temperature (600–800 °C), due to its ionic conductivity which is higher than that of YSZ (Yttrium Stabilized Zirconia) electrolyte. For this reason they are very promising materials as solid electrolyte for SOFCs. Synthesis of functional nanoparticles is a challenge in the nanotechnology. In this work, apatite-type lanthanum silicate nanoparticles were synthesized by a water-based sol–gel process, i.e., sol–gel technique followed by chemical precipitation of lanthanum hydroxide on the gel of the silica. Na{sub 2}SiO{sub 3} waste solution was used as silica source. Spherical aerogel silica was prepared by acid catalyzed reaction, followed by precipitation of lanthanum hydroxide to obtain the precursor of apatite-type lanthanum silicate. Powders of apatite-type lanthanum silicate achieved from the precursor were characterized by thermal analysis, X-ray diffraction (XRD), scanning electron microscopy (SEM) and specific surface area measurements (BET). The apatite phase was formed at 900 °C.

  20. Sulfur concentration and isotopic variation in apatites from granitic to granodioritic plutons of a Cretaceous Cordilleran Batholith

    NASA Astrophysics Data System (ADS)

    Economos, R. C.

    2012-12-01

    Apatite is a common igneous accessory mineral with a high saturation temperature which can therefore crystallize over a significant portion of magmatic compositional space. Sulfur presents an opportunity to identify zoning in apatites. Unlike other trace elements, sulfur is relatively immobile in the apatite crystal structure and can be present in typical concentrations up to 1500 - 2000 ppm (or 0.5 to 1 wt% SO3). Sulfur concentration zoning in igneous apatites from ore producing magmatic systems has been identified (Streck and Dilles, 1998), but the interpretation of the cause of this zoning remains an open question. δ34S isotopic ratios of whole apatites have been used to track isotopic evolution associated with changes in magma fO2 and eruptive degassing (Rye, 2005). The presented work combines sulfur concentration mapping in zoned apatite crystals with in-situ SIMS 34S and 32S isotope measurements. Apatites were extracted from granite to granodiorite samples from the Cadiz Valley Batholith in the central Mojave Desert. This batholith is related to the pulse of Cretaceous Cordilleran magmatism that generated large batholiths in the Sierra Nevada and the Penninsular Ranges. The Mojave segment of the Cretaceous arc is unique in their construction into a full thickness of continental crust which exerted a strong influence on magmatic compositions. Apatite grains were mounted parallel to C axes, ground until grains were approximately bisected, and analyzed by Electron Microprobe at UCLA, for CaO, P2O5, SO3 and SiO2. Grains were surveyed and those yielding anomalous SO3 contents were investigated by micron-scale concentration mapping. Typical SO3 concentrations of apatites from all samples were ~0.2 wt%, while 8 to 10% of apatite grains from two samples contained cores with concentrations ranging up to 0.5 wt%. The sulfur zoning in these samples is oscillatory, in some grains representing 5 to 6 repetitions of high and low concentrations. Based on these textures

  1. Sampling and analysis plan for phase II of the Bear Creek Valley treatability study Oak Ridge Y-12 Plant, Oak Ridge, Tennessee

    SciTech Connect

    1997-05-01

    The Bear Creek Valley (BCV) Treatability Study is intended to provide site-specific data defining potential treatment technologies applicable to contaminated groundwater and surface water. This project directly supports Alternative 5 of the base action in the BCV Feasibility Study, and indirectly supports other alternatives through proof of concept. In that role, the ultimate goal is to install a treatment system that will remove uranium and nitrate from groundwater before it reaches Bear Creek. A secondary goal is the concurrent removal of technetium and several metals that impact ecological risk. This project is intended to produce hydraulic and treatment performance data required to design the treatment system to reach those goals. This project will also generate information that can be applied at other facilities within the Oak Ridge Reservation. This report is the sampling and analysis plan (SAP) for the field work component of Phase II of the BCV Treatability Study. Field work for this phase of the BCV Treatability Study consists of media testing. In-field continuous flow tests will be conducted over an extended time period (5 weeks) to generate data on long-term treatment effects on potential treatment media including sorbents and zero valent iron, over 28 weeks for constructed wetlands treatment, and over 24 weeks for algal mats treatment. The SAP addresses environmental sampling at the S-3 Site at the Oak Ridge Y-12 Plant. Samples will be taken from groundwater, effluent from test columns, effluent from an algal mat reactor, and effluent from a pilot-scale wetlands. This plan will be implemented as part of the BCV Phase II Treatability Study Best Management Practices Plan and in conjunction with the BCV Phase II Treatability Study Health and Safety Plan and the BCV Phase II Treatability Study Waste Management Plan.

  2. Evidence for Differential Unroofing in the Adirondack Mountains, New York State, Determined by Apatite Fission-Track Thermochronology.

    PubMed

    Roden-Tice; Tice; Schofield

    2000-03-01

    Apatite fission-track ages of 168-83 Ma for 39 samples of Proterozoic crystalline rocks, three samples of Cambrian Potsdam sandstone, and one Cretaceous lamprophyre dike from the Adirondack Mountains in New York State indicate that unroofing in this region occurred from Late Jurassic through Early Cretaceous. Samples from the High Peaks section of the Adirondack massif yielded the oldest apatite fission-track ages (168-135 Ma), indicating that it was exhumed first. Unroofing along the northern, northwestern, and southwestern margins of the Adirondacks began slightly later, as shown by younger apatite fission-track ages (146-114 Ma) determined for these rocks. This delay in exhumation may have resulted from burial of the peripheral regions by sediment shed from the High Peaks. Apatite fission-track ages for samples from the southeastern Adirondacks are distinctly younger (112-83 Ma) than those determined for the rest of the Adirondack region. These younger apatite fission-track ages are from a section of the Adirondacks dissected by shear zones and post-Ordovician north-northeast-trending normal faults. Differential unroofing may have been accommodated by reactivation of the faults in a reverse sense of motion with maximum compressive stress, sigma1, oriented west-northwest. A change in the orientation of the post-Early Cretaceous paleostress field is supported by a change in the trend of Cretaceous lamprophyre dikes from east-west to west-northwest. PMID:10736267

  3. Geology, alteration, age, and origin of iron oxide-apatite deposits in Upper Eocene quartz monzonite, Zanjan district, NW Iran

    NASA Astrophysics Data System (ADS)

    Nabatian, Ghasem; Ghaderi, Majid; Corfu, Fernando; Neubauer, Franz; Bernroider, Manfred; Prokofiev, Vsevolod; Honarmand, Maryam

    2014-02-01

    Iron oxide-apatite deposits are present in Upper Eocene pyroxene-quartz monzonitic rocks of the Zanjan district, northwestern Iran. Mineralization occurred in five stages: (1) deposition of disseminated magnetite and apatite in the host rock; (2) mineralization of massive and banded magnetite ores in veins and stockwork associated with minor brecciation and calcic alteration of host rocks; (3) deposition of sulfide ores together with potassic alteration; (4) formation of quartz and carbonate veins and sericite, chlorite, epidote, silica, carbonate, and tourmaline alteration; and (5) supergene alteration and weathering. U-Pb dating of monazite inclusions in the apatite indicates an age of 39.99 ± 0.24 Ma, which is nearly coeval with the time of emplacement of the host quartz monzonite, supporting the genetic connection. Fluid inclusions in the apatite have homogenization temperatures of about 300 °C and oxygen isotopic compositions of the magnetite support precipitation from magmatic fluids. Late-stage quartz resulted from the introduction of a cooler, less saline, and isotopically depleted fluid. The iron oxide-apatite deposits in the Tarom area of the Zanjan district are typical of a magmatic-hydrothermal origin and are similar to the Kiruna-type deposits with respect to mineral assemblages, fabric and structure of the iron ores, occurrence of the ore bodies, and wall rock alteration.

  4. Apatite 4He/3He thermochronometry evidence for an ancient Grand Canyon, Colorado Plateau, USA

    NASA Astrophysics Data System (ADS)

    Flowers, R. M.; Farley, K. A.

    2012-12-01

    The very existence of Grand Canyon inspires questions about why canyons are carved, how drainage systems and landscapes evolve, and how these processes relate to the elevation gain of plateaus. Yet when and why Grand Canyon was carved have been extraordinarily controversial for more than 150 years. Over the last several decades, the dominant view for the origin of the canyon is one of rapid incision at 5-6 Ma, when detritus derived from the upstream reaches of the Colorado River system appeared in Grand Wash Trough at the Colorado River's western exit from the Colorado Plateau. The absence of such diagnostic deposits prior to 6 Ma has been used to argue that Grand Canyon was not yet excavated (e.g., Karlstrom et al., 2008). However, a variety of data hint at a more ancient age for part or all of the canyon, and it has been proposed that a smaller drainage basin in largely carbonate lithologies could explain the absence of pre-6 Ma Colorado River clastics in Grand Wash Trough even if a significant Grand Canyon were present. Most recently, apatite (U-Th)/He (AHe) thermochronometry data from western Grand Canyon were used to infer excavation of this area to within several hundred meters of its modern depth by ca. 70 Ma (Wernicke, 2011), an interpretation in direct conflict with the young canyon model. The unexpected implications of the initial Grand Canyon AHe work motivated the apatite 4He/3He and U-Th zonation study presented here. Apatite 4He/3He thermochronometry provides information about the spatial distribution of radiogenic 4He in an apatite crystal that can better constrain a sample's cooling history. A key premise of AHe and 4He/3He spectra interpretation is that the He kinetic model used is accurate. We first investigate whether differing 4He/3He spectra for apatites of variable AHe date, radiation damage, and U-Th zonation from eastern Grand Canyon yield mutually consistent thermal history results using the RDAAM kinetic model, which must be true if the

  5. Bile Acid Malabsorption After Pelvic and Prostate Intensity Modulated Radiation Therapy: An Uncommon but Treatable Condition

    SciTech Connect

    Harris, Victoria; Benton, Barbara; Sohaib, Aslam; Dearnaley, David; Andreyev, H. Jervoise N.

    2012-12-01

    Purpose: Intensity modulated radiation therapy (IMRT) is a significant therapeutic advance in prostate cancer, allowing increased tumor dose delivery and increased sparing of normal tissues. IMRT planning uses strict dose constraints to nearby organs to limit toxicity. Bile acid malabsorption (BAM) is a treatable disorder of the terminal ileum (TI) that presents with symptoms similar to radiation therapy toxicity. It has not been described in patients receiving RT for prostate cancer in the contemporary era. We describe new-onset BAM in men after IMRT for prostate cancer. Methods and Materials: Diagnosis of new-onset BAM was established after typical symptoms developed, selenium-75 homocholic acid taurine (SeHCAT) scanning showed 7-day retention of <15%, and patients' symptoms unequivocally responded to a bile acid sequestrant. The TI was identified on the original radiation therapy plan, and the radiation dose delivered was calculated and compared with accepted dose-volume constraints. Results: Five of 423 men treated in a prospective series of high-dose prostate and pelvic IMRT were identified with new onset BAM (median age, 65 years old). All reported having normal bowel habits before RT. The volume of TI ranged from 26-141 cc. The radiation dose received by the TI varied between 11.4 Gy and 62.1 Gy (uncorrected). Three of 5 patients had TI treated in excess of 45 Gy (equivalent dose calculated in 2-Gy fractions, using an {alpha}/{beta} ratio of 3) with volumes ranging from 1.6 cc-49.0 cc. One patient had mild BAM (SeHCAT retention, 10%-15%), 2 had moderate BAM (SeHCAT retention, 5%-10%), and 2 had severe BAM (SeHCAT retention, <5%). The 3 patients whose TI received {>=}45 Gy developed moderate to severe BAM, whereas those whose TI received <45 Gy had only mild to moderate BAM. Conclusions: Radiation delivered to the TI during IMRT may cause BAM. Identification of the TI from unenhanced RT planning computed tomography scans is difficult and may impede accurate

  6. Apatite fission-track thermochronology of the central and southern Appalachian Basin

    SciTech Connect

    Roden, M.K.

    1989-01-01

    Samples were collected in west to east transects across the Appalachian Basin of Pennsylvania, Maryland, West Virginia, and Virginia. These samples locations were chosen to test the concept of increasing paleotemperature due to increasing burial from west to east across the Appalachian Basin and to detect any thermal anomalies that exist. Calculated time-temperature (tT) paths based on apatite fission-track apparent ages and confined track length distributions for samples from this study indicate that both the Pennsylvania and southern Appalachian had complex uplift and cooling histories. In Pennsylvania, the Tioga and Kalkberg ash bed samples from central Pennsylvania yield modelled tT paths that indicate early post-Alleghanian (285-270 Ma) cooling with uplift estimated at beginning at {approx}251 {plus minus} 25 Ma. Samples from the western Allegheny Plateau and Allegheny Front contain apatites which have reset to give fission-track ages and track lengths consistent with tT histories beginning at <200 Ma. In northeastern Pennsylvania on the Allegheny Plateau, the modelled tT paths show rapid cooling from temperatures in the range of 110{degree}-120{degree} C at 170-160 Ma. In the southern Appalachian Basin, calculated tT paths indicate that uplift in the northern section was immediately post-Alleghanian folding with uplift beginning first in the northwestern section on the Cumberland Plateau at {approx}226 {plus minus} 23 Ma and progressing to the eastern Valley and Ridge Province of Virginia at {approx}119 {plus minus} 12 Ma. The samples from southwestern Virginia yield a mean apatite fission-track apparent age of 175 {plus minus} 11 Ma which may be the result of a higher heat flow, higher paleogeothermal gradient during the Upper Jurassic-Early Cretaceous extension along the Atlantic Coast.

  7. Fungal Bioweathering of Mimetite and a General Geomycological Model for Lead Apatite Mineral Biotransformations

    PubMed Central

    Ceci, Andrea; Kierans, Martin; Hillier, Stephen; Persiani, Anna Maria

    2015-01-01

    Fungi play important roles in biogeochemical processes such as organic matter decomposition, bioweathering of minerals and rocks, and metal transformations and therefore influence elemental cycles for essential and potentially toxic elements, e.g., P, S, Pb, and As. Arsenic is a potentially toxic metalloid for most organisms and naturally occurs in trace quantities in soil, rocks, water, air, and living organisms. Among more than 300 arsenic minerals occurring in nature, mimetite [Pb5(AsO4)3Cl] is the most stable lead arsenate and holds considerable promise in metal stabilization for in situ and ex situ sequestration and remediation through precipitation, as do other insoluble lead apatites, such as pyromorphite [Pb5(PO4)3Cl] and vanadinite [Pb5(VO4)3Cl]. Despite the insolubility of mimetite, the organic acid-producing soil fungus Aspergillus niger was able to solubilize mimetite with simultaneous precipitation of lead oxalate as a new mycogenic biomineral. Since fungal biotransformation of both pyromorphite and vanadinite has been previously documented, a new biogeochemical model for the biogenic transformation of lead apatites (mimetite, pyromorphite, and vanadinite) by fungi is hypothesized in this study by application of geochemical modeling together with experimental data. The models closely agreed with experimental data and provided accurate simulation of As and Pb complexation and biomineral formation dependent on, e.g., pH, cation-anion composition, and concentration. A general pattern for fungal biotransformation of lead apatite minerals is proposed, proving new understanding of ecological implications of the biogeochemical cycling of component elements as well as industrial applications in metal stabilization, bioremediation, and biorecovery. PMID:25979898

  8. The status of strontium in biological apatites: an XANES/EXAFS investigation.

    PubMed

    Bazin, Dominique; Dessombz, Arnaud; Nguyen, Christelle; Ea, Hang Korng; Lioté, Frédéric; Rehr, John; Chappard, Christine; Rouzière, Stephan; Thiaudière, Dominique; Reguer, Solen; Daudon, Michel

    2014-01-01

    Osteoporosis represents a major public health problem through its association with fragility fractures. The public health burden of osteoporotic fractures will rise in future generations, due in part to an increase in life expectancy. Strontium-based drugs have been shown to increase bone mass in postmenopausal osteoporosis patients and to reduce fracture risk but the molecular mechanisms of the action of these Sr-based drugs are not totally elucidated. The local environment of Sr(2+) cations in biological apatites present in pathological and physiological calcifications in patients without such Sr-based drugs has been assessed. In this investigation, X-ray absorption spectra have been collected for 17 pathological and physiological calcifications. These experimental data have been combined with a set of numerical simulations using the ab initio FEFF9 X-ray spectroscopy program which takes into account possible distortion and Ca/Sr substitution in the environment of the Sr(2+) cations. For selected samples, Fourier transforms of the EXAFS modulations have been performed. The complete set of experimental data collected on 17 samples indicates that there is no relationship between the nature of the calcification (physiological and pathological) and the adsorption mode of Sr(2+) cations (simple adsorption or insertion). Such structural considerations have medical implications. Pathological and physiological calcifications correspond to two very different preparation procedures but are associated with the same localization of Sr(2+) versus apatite crystals. Based on this study, it seems that for supplementation of Sr at low concentration, Sr(2+) cations will be localized into the apatite network. PMID:24365928

  9. Evaluating apatite formation and osteogenic activity of electrospun composites for bone tissue engineering.

    PubMed

    Patlolla, Ajitha; Arinzeh, Treena Livingston

    2014-05-01

    Significant interest has been in examining calcium phosphate ceramics, specifically β-tricalcium phosphate (β-TCP) (Ca3 (PO4)2 ) and synthetic hydroxyapatite (HA) (Ca10 (PO4)6 (OH)2 ), in composites and more recently, in fibrous composites formed using the electrospinning technique for bone tissue engineering applications. Calcium phosphate ceramics are sought because they can be bone bioactive, which means an apatite forms on their surface that facilitates bonding to bone tissue, and are osteoconductive. However, studies examining the bioactivity of electrospun composites containing calcium phosphates and their corresponding osteogenic activity have been limited. In this study, electrospun composites consisting of (20/80) HA/TCP nanoceramics and poly (ϵ-caprolactone) (PCL) were fabricated. Solvent and solvent combinations were evaluated to form scaffolds with a maximum concentration and dispersion of ceramic and pore sizes large enough for cell infiltration and tissue growth. PCL was dissolved in either methylene chloride (Composite-MC) or a combination of methylene chloride (80%) and dimethylformamide (20%; Composite-MC + DMF). Composites were evaluated in vitro for degradation, apatite formation, and osteogenic differentiation of human mesenchymal stem cells (MSCs) with an emphasis on temporal gene expression of osteogenic markers and the pluripotent gene Sox-2. Apatite formation and the osteogenic differentiation was the greatest for Composite-MC as determined by gene expression, protein production and biochemical markers, even without the presence of osteoinductive factors in the media, in comparison to Composite-MC + DMF and unfilled PCL mats. Sox-2 levels also reduced over time. The results of this study demonstrate that the solvent or solvent combination used in preparing the electrospun composite mats plays a critical role in determining their bioactivity which may, in turn, affect cell behavior. PMID:24264603

  10. Rare earth element distributions in recent and fossil apatite: implications for paleoceanography and stratigraphy

    SciTech Connect

    Wright, J.

    1985-01-01

    Rare earth element (REE) distributions in biogenic apatite were determined in over 200 samples from Cambrian to the Recent. Nondestructive instrumental neutron activation analysis techniques were adapted for analysis of low-mass microfossil samples. Tests for chemical contamination, interspecies, interlaboratory and interexperiment variations show that there is no fractionation of REE, so that ratios of rare earths are consistent throughout the entire group of samples. The REE signature of biogenic apatite is acquired after deposition but only at the sediment-water interface and is characteristic of the redox state of the environment of deposition. This original environmental signature is retained through subsequent burial and diagenesis. Cerium has been shown to be the rare earth element that is sensitive to oxidation-reduction variations in marine waters. This cerium variation is stated mathematically and called Ce/sub anom/. Comparison of Ce/sub anom/ in fish debris from different modern redox environments shows that values > -0.10 occur in fish debris deposited under reducing conditions, whereas Ce/sub anom/ values <-0.10 are obtained under oxidizing conditions. Paleoredox studies of Ce/sub anom/ of fossil apatite of conodonts, fish debris and inarticulate brachiopods indicate that significant shifts in the overall redox balance of seawater occurred in ancient oceans. Cambrian through Silurian seas were dominated by anoxia, followed by a gradual change to oxidizing conditions in the Devonian. Oceans remained generally oxidizing throughout the Carboniferous and Lower Permian. In the Upper Permian and Lower Triassic anoxic conditions were again prevalent. This was followed by a return to an oxidizing oceanic environment in the Upper Triassic.

  11. A Bayesian approach to calibrating apatite fission track annealing models for laboratory and geological timescales

    NASA Astrophysics Data System (ADS)

    Stephenson, John; Gallagher, Kerry; Holmes, Chris

    2006-10-01

    We present a new approach for modelling annealing of fission tracks in apatite, aiming to address various problems with existing models. We cast the model in a fully Bayesian context, which allows us explicitly to deal with data and parameter uncertainties and correlations, and also to deal with the predictive uncertainties. We focus on a well-known annealing algorithm [Laslett, G.M., Green, P.F., Duddy, I.R., Gleadow. A.J.W., 1987. Thermal annealing of fission tracks in apatite. 2. A quantitative-analysis. Chem. Geol., 65 (1), 1-13], and build a hierachical Bayesian model to incorporate both laboratory and geological timescale data as direct constraints. Relative to the original model calibration, we find a better (in terms of likelihood) model conditioned just on the reported laboratory data. We then include the uncertainty on the temperatures recorded during the laboratory annealing experiments. We again find a better model, but the predictive uncertainty when extrapolated to geological timescales is increased due to the uncertainty on the laboratory temperatures. Finally, we explictly include a data set [Vrolijk, P., Donelick, R.A., Quenq, J., Cloos. M., 1992. Testing models of fission track annealing in apatite in a simple thermal setting: site 800, leg 129. In: Larson, R., Lancelet, Y. (Eds.), Proceedings of the Ocean Drilling Program, Scientific Results, vol. 129, pp. 169-176] which provides low-temperature geological timescale constraints for the model calibration. When combined with the laboratory data, we find a model which satisfies both the low-temperature and high-temperature geological timescale benchmarks, although the fit to the original laboratory data is degraded. However, when extrapolated to geological timescales, this combined model significantly reduces the well-known rapid recent cooling artifact found in many published thermal models for geological samples.

  12. Colocation and role of polyphosphates and alkaline phosphatase in apatite biomineralization of elasmobranch tesserae.

    PubMed

    Omelon, Sidney; Georgiou, John; Variola, Fabio; Dean, Mason N

    2014-09-01

    Elasmobranchs (e.g. sharks and rays), like all fishes, grow continuously throughout life. Unlike other vertebrates, their skeletons are primarily cartilaginous, comprising a hyaline cartilage-like core, stiffened by a thin outer array of mineralized, abutting and interconnected tiles called tesserae. Tesserae bear active mineralization fronts at all margins and the tesseral layer is thin enough to section without decalcifying, making this a tractable but largely unexamined system for investigating controlled apatite mineralization, while also offering a potential analog for endochondral ossification. The chemical mechanism for tesserae mineralization has not been described, but has been previously attributed to spherical precursors, and alkaline phosphatase (ALP) activity. Here, we use a variety of techniques to elucidate the involvement of phosphorus-containing precursors in the formation of tesserae at their mineralization fronts. Using Raman spectroscopy, fluorescence microscopy and histological methods, we demonstrate that ALP activity is located with inorganic phosphate polymers (polyP) at the tessera-uncalcified cartilage interface, suggesting a potential mechanism for regulated mineralization: inorganic phosphate (Pi) can be cleaved from polyP by ALP, thus making Pi locally available for apatite biomineralization. The application of exogenous ALP to tissue cross-sections resulted in the disappearance of polyP and the appearance of Pi in uncalcified cartilage adjacent to mineralization fronts. We propose that elasmobranch skeletal cells control apatite biomineralization by biochemically controlling polyP and ALP production, placement and activity. Previous identification of polyP and ALP shown previously in mammalian calcifying cartilage supports the hypothesis that this mechanism may be a general regulating feature in the mineralization of vertebrate skeletons. PMID:24948547

  13. Authigenic apatite formation and burial in sediments from non-upwelling, continental margin environments

    SciTech Connect

    Ruttenberg, K.C.; Berner, R.A. )

    1993-03-01

    Evidence for precipitation of authigenic carbonate fluorapatite (CFA) in Long Island Sound and Mississippi Delta sediments suggests that formation of CFA is not restricted to environments of active coastal upwelling. The authors present porewater data suggestive of CFA formation in both these areas. Application of a sequential leaching procedure, designed specifically to separate authigenic carbonate fluorapatite from other phosphorus-containing phases, including detrital apatite of igneous or metamorphic origin, provides strong supporting evidence for authigenic apatite formation in these sediments. The size of the authigenic apatite reservoir increases with depth, indicating continued formation of CFA during early diagenesis. This depth increase is mirrored by a decrease in solid-phase organic P at both sites, suggesting that CFA is forming at the expense of organic P. Mass balance considerations, application of diagenetic models to intersitital water nutrient data, and the saturation state of the interstitial water are consistent with this interpretation. Diagenetic redistribution of phosphorus among the different solid-phase reservoirs is observed at both sites, and results in near perfect retention of P by these sediments over the depth intervals sampled. Formation of CFA in continental margins which do not conform to the classically defined regions of phosphorite formation renders CFA a quantitatively more important sink than has previously been recognized. Including this reservoir as a newly identified sink for reactive P in the ocean, the residence time of P in the modern ocean must be revised downward. The implication for ancient oceans of CFA formation in continental margin sediments other than phosphorites is that phosphorite formation may be less a representation of episodicity in removal of reactive P from the oceans than of localized concentration of CFA in phosphatic sediments by secondary physical processes. 90 refs., 5 figs., 2 tabs.

  14. Secular changes in the oxygen isotopic composition of Devonian biogenic apatite

    NASA Astrophysics Data System (ADS)

    Breisig, S.; Joachimski, M. M.; Buggisch, W.

    2003-04-01

    Oxygen isotopes are a key tool for quantifying temperature and salinity of ancient sea water. Initially, pristine skeletal carbonates (preferentially LMC) have been utilized to monitor variations in the oxygen isotopic composition of past oceans. A high preservation potential of the primordial isotopic signature may also be awarded to conodonts. These microfossils consist of fluor-apatite (francolite) with a dense microcrystalline structure and therefore are comparatively insensitive with regard to diagenetic overprinting. Because conodonts are frequent in Devonian rocks and widely used as index fossils, their application for oxygen isotope analysis is espe-cially promising for this specific geological time interval. Laser-based microsampling or high-temperature combustion techniques (TC/EA) allows us to analyse microsamples of conodont apatite (0.5 to 1 mg). The oxygen isotope measurements are performed on trisilverphosphate after dissolving conodont apatite (0.5 to 1 mg) in nitric acid and precipitating the phosphate group as Ag_3PO_4. Conodont samples from different locations in Germany (Rheinisches Schieferge-birge) and the Czech Republic (Prague Basin) as well as from the United States (Iowa) and Morocco (Anti-Atlas) have been analysed. δ18Oapatite values are presented for the Lochkovian, Middle and Late Devonian. δ18Oapatite values for the Lochkovian (Prague Basin) vary between 18.5 and 19.0 ppm (δ18Oapatite values given in V-SMOW). Assuming an oxygen isotopic composition for Devonian seawater of -1 ppm (ice-free world), the δ18Oapatite values translate into tem-peratures of 26^o to 28^oC for the tropical Lochkovian ocean. Eifelian to Givetian conodonts (Rheinisches Schiefergebirge, Prague Basin) show δ18Oapatite values from 18.5 to 20.4 ppm, corresponding to paleotemperatures of 20 to 28^o C. The Middle to Late Devonian transition is mainly documented by conodonts from Iowa with δ18Oapatite values of 18 to 20 ppm (21-30^o C). Conodont δ18Oapatite

  15. Unroofing History of the Colorado Plateau From (U-Th)/He Apatite Thermochronology

    NASA Astrophysics Data System (ADS)

    Flowers, R. M.; Wernicke, B. P.; Farley, K. A.

    2006-12-01

    The timing and mechanism of uplift of the Colorado Plateau by ~1.9 km since the Cretaceous is a major question in Cordilleran tectonics. Resolving when the Colorado Plateau was unroofed can provide some insight into this problem, because erosional denudation commonly is linked with uplift. New (U-Th)/He apatite data constrain post-Cretaceous denudational patterns in the Grand Canyon region of the southwestern Colorado Plateau. This area is underlain by resistant limestone of the Permian Kaibab Formation and preserves discontinuous remnants of fluvial sandstone of the Triassic Moenkopi Formation. Tertiary "rim gravels" unconformably overlie this surface near the plateau margin. Stratigraphic and apatite fission-track data suggest that the area was buried by several kilometers of Mesozoic and Cenozoic strata prior to plateau uplift and regional unroofing. (U-Th)/He dates for individual detrital apatites from fourteen Moenkopi sandstone samples across this area 1) are significantly younger than the depositional age of the unit, indicating partial to complete He loss following deposition, and 2) display dates that are younger with increasing distance from the plateau margin, reflecting an overall pattern of southwest to northeast stripping of the overlying sedimentary package. Individual apatites from five Tertiary rim gravel samples did not undergo significant He loss following deposition, such that the distributions of dates reflect the denudation of source regions and impose a maximum timing constraint on gravel deposition following unroofing to the modern plateau surface. Our results suggest that the current plateau margin was buried by > 1.5 km of Cretaceous sediments prior to pulses of denudation in the Laramide and mid-Tertiary (40-35 Ma) that may be linked with uplift episodes at these times. Each denudational pulse was followed by rim gravel aggradation. Significant late-Tertiary unroofing and scarp retreat is most simply explained by integration of the

  16. Preparation of nanocrystalline bredigite powders with apatite-forming ability by a simple combustion method

    SciTech Connect

    Huang Xianghui; Chang Jiang

    2008-06-03

    Nanocrystalline bredigite (Ca{sub 7}MgSi{sub 4}O{sub 16}) powders were synthesized by a simple solution combustion method. Phase pure bredigite powders with particle sizes ranging from 234 to 463 nm could be obtained at a relatively low temperature of 650 deg. C. The apatite-forming ability of the bredigite powders was examined by soaking them in a stimulated body fluid. The compositional and morphological changes of the powders before and after soaking were analyzed by X-ray diffraction and scanning electron microscopy and the results showed that hydroxyapatite was formed after soaking for 4 days.

  17. In-Situ Apatite Laser Ablation U-Th-Sm/He Dating, Methods and Challenges

    NASA Astrophysics Data System (ADS)

    Pickering, J. E.; Matthews, W.; Guest, B.; Hamilton, B.; Sykes, C.

    2015-12-01

    In-situ, laser ablation U-Th-Sm/He dating is an emerging technique in thermochronology that has been proven as a means to date zircon and monzonite1-5. In-situ U-Th-Sm/He thermochronology eliminates many of the problems and inconveniences associated with traditional, whole grain methods, including; reducing bias in grain selection based on size, shape and clarity; allowing for the use of broken grains and grains with inclusions; avoiding bad neighbour effects; and eliminating safety hazards associated with dissolution. In-situ apatite laser ablation is challenging due to low concentrations of U and Th and thus a low abundance of radiogenic He. For apatite laser ablation to be effective the ultra-high-vacuum (UHV) line must have very low and consistent background levels of He. To reduce He background, samples are mounted in a UHV stable medium. Our mounting process uses a MicroHePP (Microscope Mounted Heated Platen Press) to press samples into FEP (fluorinated ethylene propylene) bonded to an aluminum backing plate. Samples are ablated using a Resonetics 193 nm excimer laser and liberated He is measured using a quadrupole mass spectrometer on the ASI Alphachron noble gas line; collectively this system is known as the Resochron. The ablated sites are imaged using a Zygo Zescope optical profilometer and ablated pit volume measured using PitVol, a custom MatLab algorithm developed to enable precise and unbiased measurement of the ablated pit geometry. We use the well-characterized Durango apatite to demonstrate the accuracy and precision of the method. He liberated from forty-two pits, having volumes between 1700 and 9000 um3, were measured using the Resochron. The ablated sites were imaged using a Zygo Zescope optical profilometer and ablated pit volume measured using PitVol. U, Th and Sm concentrations were measured by laser ablation and the U-Th-Sm/He age calculated by standard age equation. An age of 33.8±0.31 Ma was determined and compares well with conventional

  18. Extraction of rare earth elements from hydrate-phosphate precipitates of apatite processing

    NASA Astrophysics Data System (ADS)

    Andropov, M. O.; Anufrieva, A. V.; Buynovskiy, A. S.; Makaseev, Y. N.; Mazov, I. N.; Nefedov, R. A.; Sachkov, V. I.; Stepanova, O. B.; Valkov, AV

    2016-01-01

    The features of extraction of rare earth elements (REE) were considered from hydrate-phosphate precipitates of REE of apatite processing by nitric acid technology. The preliminary purification of nitrate solution of REE from impurities of titanium, aluminum, iron, uranium and thorium was suggested to obtain stable solutions not forming precipitates. Washing the extract was recommended with the evaporated reextract that allows to obtain directly on the cascade of REE extraction the concentrated solutions suitable for the separation into groups by the extraction method. Technical decisions were suggested for the separation of REE in groups without the use of salting-out agent.

  19. Thermodynamic Properties of Sulfatian Apatite: Constraints on the Behavior of Sulfur in Calc-Alkaline Magmas

    NASA Astrophysics Data System (ADS)

    Core, D.; Essene, E. J.; Luhr, J. F.; Kesler, S. E.

    2004-12-01

    The Gibbs free energy of hydroxyellestadite [Ca10(SiO4)3(SO4)3(OH)2] was estimated using mineral equilibria applied to analyzed assemblages from the experimental charges of Luhr (1990). The apatite analyses of Peng et al. (1997) were used in conjunction with new analyses of the oxides and silicates in this study. An ideal mixing model was employed for apatite combined with mixing models from MELTS (Ghiorso & Sack, 1994) and Gibbs free energy data from Robie & Hemingway (1995) for the other crystalline phases. The resultant equation of the Gibbs free energy vs. T for hydroxyellestadite is as follows: DG°T(elem) = [2.817(T - 273) - 11831]/1000 kJ/mol, T in K. The calculated entropy for hydroxyellestadite is 1944 J/mol.K at 1073 K and 2151 J/mol.K at 1227 K. Independent estimates of the entropy of hydroxyellestadite obtained with the method of Robinson & Haas (1983) are within 5% of these values. The thermodynamic data on hydroxyellestadite were used to calculate the locus of the reactions: 2Ca10(SiO4)3(SO4)3(OH)2 + 7S2 + 21O2 = 20CaSO4 + 6SiO2 + 2H2O 6Ca10(SiO4)3(SO4)3(OH)2 + 102SiO2 + 20Fe3O4 = 60CaFeSi2O6 + 6H2O + 9S2 + 37O2 2Ca10(SiO4)3(SO4)3(OH)2 + 10Mg2Si2O6 + 14SiO2 = 20CaMgSi2O6 + 2H2O + 3S2 + 9O2 in fO2-fS2 space at fixed P-T. Application of these equilibria to apatite zoned in sulfate from oxidized granitoids reflects a drop in fS2 by more than 1 log unit during its growth. The zoning is interpreted to represent the removal of a magmatic vapor phase during crystallization of these plutons. Removal of sulfur from magmas by hydrothermal fluids is important to the ore-forming process and to the production of acid sulfate aerosols during eruption of oxidized magmas. Preservation of sulfatian apatite may yield data on the sulfidation states of ancient flood basalts such as the Deccan Traps of India and the Parana basalts of Brazil to address the environmental impact of these giant eruptions.

  20. Taking Stock and Taking Steps: The Case for an Adolescent Version of the Short-Assessment of Risk and Treatability

    PubMed Central

    Viljoen, Jodi L.; Cruise, Keith R.; Nicholls, Tonia L.; Desmarais, Sarah L.; Webster, Christopher

    2012-01-01

    The field of violence risk assessment has matured considerably, possibly advancing beyond its own adolescence. At this point in the field’s evolution, it is more important than ever for the development of any new device to be accompanied by a strong rationale and the capacity to provide a unique contribution. With this issue in mind, we first take stock of the field of adolescent risk assessment in order to describe the rapid progress that this field has made, as well as the gaps that led us to adapt the Short-Term Assessment of Risk and Treatability (START; Webster, Martin, Brink, Nicholls, & Desmarais, 2009) for use with adolescents. We view the Short-Term Assessment of Risk and Treatability: Adolescent Version (START:AV; Nicholls, Viljoen, Cruise, Desmarais, & Webster, 2010; Viljoen, Cruise, Nicholls, Desmarais, & Webster, in progress) as complementing other risk measures in four primary ways: 1) rather than focusing solely on violence risk, it examines broader adverse outcomes to which some adolescents are vulnerable (including self-harm, suicide, victimization, substance abuse, unauthorized leave, self-neglect, general offending); 2) it places a balanced emphasis on adolescents’ strengths; 3) it focuses on dynamic factors that are relevant to short-term assessment, risk management, and treatment planning; and 4) it is designed for both mental health and justice populations. We describe the developmentally-informed approach we took in the adaptation of the START for adolescents, and outline future steps for the continuing validation and refinement of the START:AV. PMID:23436982

  1. Evaluation of fall chinook salmon spawning adjacent to the In-Situ Redox Manipulation treatability test site, Hanford Site, Washington

    SciTech Connect

    Mueller, R.P.; Geist, D.R.

    1998-10-02

    The In Situ Redox Manipulation (ISRM) experiment is being evaluated as a potential method to remove contaminants from groundwater adjacent to the Columbia River near the 100-D Area. The ISRM experiment involves using sodium dithionate (Na{sub 2}O{sub 6}S{sub 2}) to precipitate chromate from the groundwater. The treatment will likely create anoxic conditions in the groundwater down-gradient of the ISRM treatability test site; however, the spatial extent of this anoxic plume is not exactly known. Surveys were conducted in November 1997, following the peak spawning of fall chinook salmon. Aerial surveys documented 210 redds (spawning nests) near the downstream island in locations consistent with previous surveys. Neither aerial nor underwater surveys documented fall chinook spawning in the vicinity of the ISRM treatability test site. Based on measurements of depth, velocity, and substrate, less than 1% of the study area contained suitable fall chinook salmon spawning habitat, indicating low potential for fall chinook salmon to spawn in the vicinity of the ISRM experiment.

  2. Frequency of dementia syndromes with a potentially treatable cause in geriatric in-patients: analysis of a 1-year interval.

    PubMed

    Djukic, Marija; Wedekind, Dirk; Franz, Almuth; Gremke, Melanie; Nau, Roland

    2015-08-01

    In addition to neurodegenerative and vascular causes of dementia, in the differential diagnosis potentially reversible conditions of dementia also must be assessed. Routine laboratory parameters and neuroimaging, which are recommended for the differential diagnosis of suspected dementia by the German S3 Guideline "Dementia", were retrospectively studied in 166 geriatric patients with suspected dementia. Delirium was diagnosed in six patients (3.6%). These six patients were excluded from the study. Of the 160 remaining patients, there were 99 (59.6%) with an already known dementia. In this subgroup of patients, we found a potentially treatable cause of dementia in 18.2%. In the remaining 61 patients (36.8%), the newly diagnosed dementia syndrome was established according to ICD-10 criteria. Potentially reversible causes of the dementia syndrome were found in 19 of these patients (31.1%). The most common cause was depressive pseudodementia in eight patients followed by vitamin B12 deficiency in six patients. A significant amount of our patients showed laboratory or imaging changes suggestive of potentially reversible causes of the dementia syndrome upon admission. The results of our study indicate the importance of careful differential diagnosis of dementia based on the recommendations of guidelines. Although therapy of these potential causes is not always accompanied by a full recovery, the identification and therapy of treatable causes of cognitive deficits are possible even for general practitioners, who often are the primary contact persons of affected individuals. PMID:25716929

  3. Formation of apatite oxynitrides by the reaction between apatite-type oxide ion conductors, La{sub 8+x}Sr{sub 2-x}(Si/Ge){sub 6}O{sub 26+x/2}, and ammonia

    SciTech Connect

    Orera, A.; Headspith, D.; Apperley, D.C.; Francesconi, M.G.; Slater, P.R.

    2009-12-15

    Following growing interest in the use of ammonia as a fuel in solid oxide fuel cells (SOFCs), we have investigated the possible reaction between the apatite silicate/germanate electrolytes, La{sub 8+x}Sr{sub 2-x}(Si/Ge){sub 6}O{sub 26+x/2,} and NH{sub 3} gas. We examine how the composition of the apatite phase affects the reaction with ammonia. For the silicate series, the results showed a small degree of N incorporation at 600 deg. C, while at higher temperatures (800 deg. C), substantial N incorporation was observed. For the germanate series, partial decomposition was observed after heating in ammonia at 800 deg. C, while at the lower temperature (600 deg. C), significant N incorporation was observed. For both series, the N content in the resulting apatite oxynitride was shown to increase with increasing interstitial oxide ion content (x/2) in the starting oxide. The results suggest that the driving force for the nitridation process is to remove the interstitial anion content, such that for the silicates the total anion (O+N) content in the oxynitrides approximates to 26.0, the value for an anion stoichiometric apatite. For the germanates, lower total anion contents are observed in some cases, consistent with the ability of the germanates to accommodate anion vacancies. The removal of the mobile interstitial oxide ions on nitridation suggests problems with the use of apatite-type electrolytes in SOFCs utilising NH{sub 3} at elevated temperatures. - Graphical abstract: In this paper we show that heating the apatite-type electrolytes La{sub 8+x}Sr{sub 2-x}(Si/Ge){sub 6}O{sub 26+x/2} in NH{sub 3} at high temperatures leads to nitridation of the electrolyte, with the level of nitridation increasing with increasing x.

  4. Apatite U-Pb Thermochronology: A combined ID-TIMS and LA-ICP-MS study from southern Ecuador

    NASA Astrophysics Data System (ADS)

    Cochrane, R.; Spikings, R.; Chew, D.; Wotzlaw, J.

    2012-04-01

    A combination of U-Pb LA-ICP-MS and ID-TIMS analyses of apatite has been used to investigate the high temperature (>450° C) thermal history of the Ecuadorian Andean margin. The rocks of the Eastern Cordillera of Ecuador evolved via terrane collision and accretion events, and active margin magmatism since the Early Jurassic. Low temperature (0.5) reveal periods of: i) rapid cooling (~240-220 Ma) through the Pb Partial Retention Zone (PRZ) shortly after crystallization, ii) residence at temperatures lower than the PRZ throughout the Jurassic, iii) reheating during 140-90 Ma, and iv) rapid cooling starting at 80-70 Ma. These findings corroborate conclusions based on geochronological and sedimentological data. Additional in-situ age transects and age-depth profiling of apatite are scheduled to determine the concentration distribution of radiogenic lead in the apatites, which will be used to constrain further the mechanisms of lead loss.

  5. Possible secondary apatite fission track age standard from altered volcanic ash beds in the middle Jurassic Carmel Formation, Southwestern Utah

    USGS Publications Warehouse

    Kowallis, B.J.; Christiansen, E.H.; Everett, B.H.; Crowley, K.D.; Naeser, C.W.; Miller, D.S.; Deino, A.L.

    1993-01-01

    Secondary age standards are valuable in intra- and interlaboratory calibration. At present very few such standards are available for fission track dating that is older than Tertiary. Several altered volcanic ash beds occur in the Middle Jurassic Carmel Formation in southwestern Utah. The formation was deposited in a shallow marine/sabhka environment. Near Gunlock, Utah, eight ash beds have been identified. Sanidines from one of the ash beds (GUN-F) give a single-crystal laser-probe 40Ar/39Ar age of 166.3??0.8 Ma (2??). Apatite and zircon fission track ages range from 152-185 Ma with typically 15-20 Ma errors (2??). Track densities in zircons are high and most grains are not countable. Apatites are fairly common in most of the ash beds and have reasonable track densities ranging between 1.2-1.5 ?? 106 tracks/cm2. Track length distributions in apatites are unimodal, have standard deviations <1??m, and mean track lengths of about 14-14.5 ??m. High Cl apatites (F:Cl:OH ratio of 39:33:28) are particularly abundant and large in ash GUN-F, and are fairly easy to concentrate, but the concentrates contain some siderite, most of which can be removed by sieving. GUN-F shows evidence of some reworking and detriaal contamination based on older single grain 40Ar/39Ar analyses and some rounding of grains, but the apatite population appears to be largely uncontaminated. At present BJK has approximately 12 of apatite separate from GUN-F. ?? 1993.

  6. Apatite coated on organic polymers by biomimetic process: improvement in its adhesion to substrate by NaOH treatment.

    PubMed

    Tanahashi, M; Yao, T; Kokubo, T; Minoda, M; Miyamoto, T; Nakamura, T; Yamamuro, T

    1994-01-01

    A dense, uniform and highly biologically active bone-like apatite layer can be formed in arbitrary thickness on any kind and shape of solid substrate surface by the following biomimetic method at ordinary temperature and pressure. First, a substrate is set in contact with particles of bioactive CaO SiO2 based glass soaked in a simulated body fluid (SBF) with inorganic ion concentrations nearly equal to those of human blood plasma. Second, the substrate is soaked in another solution with ion concentrations 1.5 times those of SBF (1.5 SBF). In the present study, organic polymer substrates treated with 5 M NaOH solution were subjected to the above mentioned biomimetic process. The induction periods for the apatite nucleation on polyethyleneterephthalate (PET), polymethylmethacrylate (PMMA), polyamide 6 (PA6), and polyethersulfone (PESF) substrates were reduced from 24 to 12 h with the NaOH treatment. The adhesive strength of the formed apatite layer were increased from 3.5 to 8.6 MPa, from 1.1 to 3.4 MPa, and from 0.6 to 5.3 MPa with the NaOH treatment, for PET, PMMA, and PA 6, respectively. It was assumed that highly polar groups, such as carboxyl and sulfinyl ones formed by the hydrolysis of an ester group on PET and PMMA and of an amide group on PA 6, or of a sulfonyl group on PESF with the NaOH treatment, attached a large number of hydrated silica dissolved from the glass particles, to accelerate the apatite nucleation, and also to form a strong bond with the apatite. The apatite-organic polymer composites thus obtained are expected to be useful as bone-repairing as well as soft tissue-repairing materials. PMID:8580541

  7. Apatite fission-track thermochronology of the Appalachian foreland basin from the Virginia Piedmont to eastern Ohio

    SciTech Connect

    Roden, M.K. . Dept. of Earth and Environmental Science); Cerveny, P.F.; Bergman, S.C. . Research and Technical Services)

    1992-01-01

    Apatite fission-track ages have been determined for 29 samples from two transects in the southern Appalachians. The northern transect extends from the VA Piedmont northwest through the Valley and Ridge Province, Cumberland Plateau, and into the Appalachian foreland of southeastern OH. An additional transect was collected from the Pine Mountain thrust in southeastern KY extending northwest to the Cincinnati Arch. Precambrian gneisses and granites from the VA Piedmont yield reset apatite fission-track ages ranging from 103 [+-] 6 to 138 [+-] 11 Ma. Ordovician through Mississippian sedimentary rocks from the Valley and Ridge Province of VA-WV also yield reset apatite fission-track ages ranging from 120 [+-] 8 to 144 [+-] 20 Ma. The cooling histories for the Piedmont and Valley and Ridge rocks of VA and WV thus appear similar, having cooled rapidly between about 103 and 144 Ma. Pennsylvanian samples from the Cumberland Plateau of WV yield rest apatite fission-track ages of 112 [+-] 7 to 169 [+-] 13 MA in the southeast which grade into partially reset (mixed ages) northwest of Charlestown (133 [+-] 13 to 156 [+-] 10 Ma). The Permian Dunkard Formation from the OH-WV border yielded a mixed age of 197 [+-] 13 Ma, suggesting that the Permian has not been subjected to temperatures > 100 C for times greater than 1 Ma, since it was deposited. Mississippian--Pennsylvanian samples from eastern KY yield reset apatite fission-track ages which decrease from the Pine Mt. Thrust (186 [+-] 16 Ma) to Mozelle, KY (136 [+-] 12 Ma), then increase toward the Cincinnati Arch (166 [+-] 18 [minus] 186 [+-] 21 Ma). This is consistent with older apatite fission-track ages (200 Ma) from Ordovician K-bentonites in the vicinity of the Cincinnati Arch.

  8. Gelatin-apatite bone mimetic co-precipitates incorporated within biopolymer matrix to improve mechanical and biological properties useful for hard tissue repair.

    PubMed

    Won, Jong-Eun; El-Fiqi, Ahmed; Jegal, Seung-Hwan; Han, Cheol-Min; Lee, Eun-Jung; Knowles, Jonathan C; Kim, Hae-Won

    2014-04-01

    Synthetic biopolymers are commonly used for the repair and regeneration of damaged tissues. Specifically targeting bone, the composite approach of utilizing inorganic components is considered promising in terms of improving mechanical and biological properties. We developed gelatin-apatite co-precipitates which mimic the native bone matrix composition within poly(lactide-co-caprolactone) (PLCL). Ionic reaction of calcium and phosphate with gelatin molecules enabled the co-precipitate formation of gelatin-apatite nanocrystals at varying ratios. The gelatin-apatite precipitates formed were carbonated apatite in nature, and were homogeneously distributed within the gelatin matrix. The incorporation of gelatin-apatite significantly improved the mechanical properties, including tensile strength, elastic modulus and elongation at break, and the improvement was more pronounced as the apatite content increased. Of note, the tensile strength increased to as high as 45 MPa (a four-fold increase vs. PLCL), the elastic modulus was increased up to 1500 MPa (a five-fold increase vs. PLCL), and the elongation rate was ~240% (twice vs. PLCL). These results support the strengthening role of the gelatin-apatite precipitates within PLCL. The gelatin-apatite addition considerably enhanced the water affinity and the acellular mineral-forming ability in vitro in simulated body fluid; moreover, it stimulated cell proliferation and osteogenic differentiation. Taken together, the GAp-PLCL nanocomposite composition is considered to have excellent mechanical and biological properties, which hold great potential for use as bone regenerative matrices. PMID:23985536

  9. Biomimetic growth and substrate dependent mechanical properties of bone like apatite nucleated on Ti and magnetron sputtered TiO2 nanostructure

    NASA Astrophysics Data System (ADS)

    Sarma, Bimal K.; Das, Apurba; Barman, Pintu; Pal, Arup R.

    2016-04-01

    This report presents findings on biomimetic growth of hydroxyapatite (HAp) nanocrystals on Ti and sputtered TiO2 substrates. The possibility of TiO2 nanostructure as candidate materials for future biomedical applications has been explored through the comparison of microstructural and mechanical properties of bone like apatite grown on Ti and nano-TiO2 surfaces. Raman spectroscopy and x-ray diffraction studies reveal formation of carbonate apatite with apparent domain size in the nanoscale range. A better interaction at the nano-TiO2/nano-HAp interface due to higher interfacial area could promote the growth of bone like apatite. The crystal phases, crystallinity, and surface morphology of nano-TiO2 are considered as parameters to understand the nucleation and growth of apatite with different mechanical properties at the nanoscale. The methodology of x-ray line profile analysis encompasses deconvolution of merged peaks by preserving broadening due to nanosized HAp aggregates. The Young’s modulus of bone like apatite exhibits crystallographic directional dependence which suggests the presence of elastic anisotropy in bone like apatite. The lattice contraction in the c-direction is associated with the degree of carbonate substitution in the apatite lattice. The role of residual stress is critical for the lattice distortion of HAp deposited at physiological conditions of temperature and pH of human blood plasma. The ion concentration is crucial for the uniformity, crystallinity, and mechanical behaviour of the apatite.

  10. Apatite as an indicator of fluid salinity: An experimental study of chlorine and fluorine partitioning in subducted sediments

    NASA Astrophysics Data System (ADS)

    Li, Huijuan; Hermann, Joerg

    2015-10-01

    In order to constrain the salinity of subduction zone fluids, piston-cylinder experiments have been conducted to investigate the partitioning behaviour of Cl and F in subducted sediments. These experiments were performed at H2O-undersaturated conditions with a synthetic pelite starting composition containing 800 ppm Cl, over a pressure and temperature range of 2.5-4.5 GPa and 630-900 °C. Repetitive experiments were conducted with 1900 ppm Cl + 1000 ppm F, and 2100 ppm Cl. Apatite represents the most Cl-abundant mineral phase, with Cl concentration varying in the range 0.1-2.82 wt%. Affinity for Cl decreases over the following sequence: aqueous fluid > apatite ⩾ melt > other hydrous minerals (phengite, biotite and amphibole). It was found that addition of F to the Cl-bearing starting composition significantly lowers the Cl partition coefficients between apatite and melt (DClAp-melt) and apatite and aqueous fluid (DClAp-aq). Cl-OH exchange coefficients between apatite and melt (KdCl-OHAp-melt) and apatite and aqueous fluid (KdCl-OHAp-aq) were subsequently calculated. KdCl-OHAp-melt was found to vary from 1 to 58, showing an increase with temperature and a decrease with pressure and displaying a regular decrease with increasing H2O content in melt. Mole fractions of Cl and OH in melt were calculated based on an ideal mixing model for H2O, OH, O, Cl and F. The Cl contents of other hydrous minerals (phengite, biotite and amphibole) fall between 200 and 800 ppm, with resultant Cl partition coefficients from 0.02 to 0.49, appearing independent of the bulk Cl and F content. Preliminary data from this study show that the partitioning behaviour of F is strongly in favour of apatite relative to melt and phengite, with DFAp-melt = 15-51. Apatites from representative eclogite facies metasediments were examined and found to have low Cl contents close to ∼100 ppm. Calculations using our experimentally determined KdCl-OHAp-aq of 0.004 at 2.5 GPa, 630 °C indicate a low

  11. Calibration of the Fluorine, Chlorine and Hydrogen Content of Apatites With the ChemCam LIBS Instrument

    NASA Technical Reports Server (NTRS)

    Meslin, P.-Y.; Cicutto, L.; Forni, O.; Drouet, C.; Rapin, W.; Nachon, M.; Cousin, A.; Blank, J. G.; McCubbin, F. M.; Gasnault, O.; Newsom, H.; Mangold, N.; Schroeder, S.; Sautter, V.; Maurice, S.; Wiens, R. C.

    2016-01-01

    Determining the composition of apatites is important to understand the behavior of volatiles during planetary differentiation. Apatite is an ubiquitous magmatic mineral in the SNC meteorites. It is a significant reservoir of halogens in these meteorites and has been used to estimate the halogen budget of Mars. Apatites have been identified in sandstones and pebbles at Gale crater by ChemCam, a Laser-Induced Breakdown Spectroscometer (LIBS) instrument onboard the Curiosity rover. Their presence was inferred from correlations between calcium, fluorine (using the CaF molecular band centered near 603 nm, whose detection limit is much lower that atomic or ionic lines and, in some cases, phosphorus (whose detection limit is much larger). An initial quantification of fluorine, based on fluorite (CaF2)/basalt mixtures and obtained at the LANL laboratory, indicated that the excess of F/Ca (compared to the stoichiometry of pure fluorapatites) found on Mars in some cases could be explained by the presence of fluorite. Chlorine was not detected in these targets, at least above a detection limit of 0.6 wt% estimated from. Fluorapatite was later also detected by X-ray diffraction (with CheMin) at a level of approx.1wt% in the Windjana drill sample (Kimberley area), and several points analyzed by ChemCam in this area also revealed a correlation between Ca and F. The in situ detection of F-rich, Cl-poor apatites contrasts with the Cl-rich, F-poor compositions of apatites found in basaltic shergottites and in gabbroic clasts from the martian meteorite NWA 7034, which were also found to be more Cl-rich than apatites from basalts on Earth, the Moon, or Vesta. The in situ observations could call into question one of the few possible explanations brought forward to explain the SNC results, namely that Mars may be highly depleted in fluorine. The purpose of the present study is to refine the calibration of the F, Cl, OH and P signals measured by the ChemCam LIBS instrument, initiated

  12. Effect of the chemical impurities on the luminescence emission of natural apatites.

    PubMed

    Roman-Lopez, J; Correcher, V; Garcia-Guinea, J; Prado-Herrero, P; Rivera, T; Lozano, I B

    2014-05-21

    This paper reports on both cathodoluminescence (CL) and blue thermoluminescence (TL) emission of well-characterized natural Spanish and Brazilian apatites [Ca5(PO4)3(OH, F, Cl)]. Chemical analyses performed by means of Electron Microprobe Analysis (EMPA) have shown the presence of trace elements that can induce CL bands. In this sense, the apatites shown emission bands peaked at 3.26, 2.86, 2.62, 2.14, 2.02 and 1.94eV are respectively linked to substitutional Ce(3+), Tb(3+), Dy(3+), Pr(3+), Sm(3+) and Mn(2+) in structural Ca(2+) positions. The 3.18eV emission band can be associated with intrinsic electron defects on oxygen of the phosphate group (PO4)(3-). The presence of (UO2)(2+) gives rise to an emission at 2.14eV. All the studied aliquots exhibit one single UV-blue TL peak that modifies the position from one sample to another (370, 256 and 268°C) probably due to (i) the variation in the crystallinity index (from 0.88 to 1.34) and (ii) successive chemical processes such as oxidation, dehydration, dehydroxylation, and fluorine ions losses due to the thermal readout. PMID:24594886

  13. Thermal history of Michigan Basin and southern Canadian Shield from apatite fission track analysis

    SciTech Connect

    Crowley, K.D. )

    1991-01-10

    Apatite fission track ages and confined-length distributions were collected from 38 basement outcrop and 5 basement drillcore samples in order to reconstruct the Phanerozoic thermal history of the Michigan Basin and southern Canadian Shield. The apatite data indicate two periods of thermal activity in the region: Triassic heating/cooling that affected the basin and adjacent shield and Cretaceous or post-Cretaceous heating/cooling that primarily affected the basin. The magnitude, timing, and cause of Cretaceous thermal activity cannot be identified with the present data. Model calculations suggest that some of the shield samples and probably all of the basin samples were heated to temperatures of at least 90C just prior to relatively rapid cooling in the Triassic. Available stratigraphic and geochemical constraints suggest that these elevated temperatures were the result of burial by an additional 2-5 km of late Paleozoic (probably Pennsylvanian and Permian) sediments. It is likely that the basin was buried during the Alleghenian Orogeny as observed for the adjacent Appalachian Basin.

  14. Osteogenic Response to BMP-2 of hMSCs Grown on Apatite-Coated Scaffolds

    PubMed Central

    Davis, Hillary E.; Case, Erin M.; Miller, Stephanie L.; Genetos, Damian C.; Leach, J. Kent

    2011-01-01

    Osteoconductive materials play a critical role in promoting integration with surrounding bone tissue and resultant bone repair in vivo. However, the impact of 3D osteoconductive substrates coupled with soluble signals on progenitor cell differentiation is not clear. In this study, we investigated the influence of bone morphogenetic protein-2 (BMP-2) concentration on the osteogenic differentiation of human mesenchymal stem cells (hMSCs) when seeded in carbonated apatite-coated polymer scaffolds. Mineralized scaffolds were more hydrophilic and adsorbed more BMP-2 compared to nonmineralized scaffolds. Changes in alkaline phosphatase (ALP) activity within stimulated hMSCs were dependent on the dose of BMP-2 and the scaffold composition. We detected more cell-secreted calcium on mineralized scaffolds at all time points, and higher BMP-2 concentrations resulted in increased ALP and calcium levels. RUNX2 and IBSP gene expression within hMSCs was affected by both substrate and soluble signals, SP7 by soluble factors, and SPARC by substrate-mediated cues. The present data indicate that a combination of apatite and BMP-2 do not simply enhance the osteogenic response of hMSCs, but act through multiple pathways that may be both substrate- and growth factor-mediated. Thus, multiple signaling strategies will likely be necessary to achieve optimal bone regeneration. PMID:21656707

  15. A first report of hydroxylated apatite as structural biomineral in Loasaceae - plants' teeth against herbivores.

    PubMed

    Ensikat, Hans-Jürgen; Geisler, Thorsten; Weigend, Maximilian

    2016-01-01

    Biomineralization provides living organisms with various materials for the formation of resilient structures. Calcium phosphate is the main component of teeth and bones in vertebrates, whereas especially silica serves for the protection against herbivores on many plant surfaces. Functional calcium phosphate structures are well-known from the animal kingdom, but had not so far been reported from higher plants. Here, we document the occurrence of calcium phosphate biomineralization in the South-American plant group Loasaceae (rock nettle family), which have stinging trichomes similar to those of the well-known stinging nettles (Urtica). Stinging hairs and the smaller, glochidiate trichomes contained nanocrystalline hydroxylated apatite, especially in their distal portions, replacing the silica found in analogous structures of other flowering plants. This could be demonstrated by chemical, spectroscopic, and diffraction analyses. Some species of Loasaceae contained both calcium phosphate and silica in addition to calcium carbonate. The intriguing discovery of structural hydroxylated apatite in plants invites further studies, e.g., on its systematic distribution across the family, the genetic and cellular control of plant biomineralization, the properties and ultrastructure of calcium phosphate. It may prove the starting point for the development of biomimetic calcium phosphate composites based on a cellulose matrix. PMID:27194462

  16. The Lac Des Iles Palladium Deposit, Ontario, Canada. Part II. Halogen variations in apatite

    NASA Astrophysics Data System (ADS)

    Schisa, Paul; Boudreau, Alan; Djon, Lionnel; Tchalikian, Arnaud; Corkery, John

    2015-03-01

    Analysis of apatite from the Mine Block Intrusion (MBI) of the Lac des Iles Igneous Complex shows two pronounced trends in the halogens. Apatite from relatively fresh norite and melanorites from the Pd-sulfide zone contain up to 57 mol% chlorapatite endmember with significant hydroxyapatite component. In contrast, in altered rock (amphibolite and greenschist assemblages) the chlorapatite component is typically less than 10 mol% with wide variation in the F- and OH-endmember components. The latter trend is attributed to Cl loss to degassing and alteration, whereas the former is attributed to Cl enrichment in the ore-bearing rocks. It is suggested that the relatively H2O-rich and intermediate Cl content of the early igneous fluids degassed from the deeper levels of the MBI can explain the high Pd/Pt and Pd/Ir ratios of the deposit. A model is presented in which disseminated Pd-rich sulfides are initially introduced by a high-temperature magmatic fluid that also influenced crystallization to produce the gross modal variations of the igneous host rock. This high-temperature mineralization event was subsequently modified by the influx of late igneous and country fluids at amphibolite to greenschist conditions.

  17. Halogen Variations in Apatite of the Lac Des Iles Palladium Deposit, Ontario, Canada

    NASA Astrophysics Data System (ADS)

    Boudreau, A. E.

    2014-12-01

    Analysis of apatite from the Mine Block Intrusion (MBI) of the Lac des Iles Igneous Complex show two pronounced trends in the halogens. Apatite from relatively fresh norite and melanorites from the Pd-sulfide zone contain up to 57 mole % chlorapatite endmember with significant hydroxyapatite component. In contrast, in altered rock (amphibolite and greenschist assemblages) and in the more evolved barren rocks the chlorapatite component is typically less than 10 mole % with wide variation in the F- and OH-endmember components. The latter trend is attributed to Cl loss to degassing and alteration whereas the former is attributed to Cl-enrichment in the ore-bearing rocks. It is suggested that the relatively H2O-rich and intermediate Cl content of the early igneous fluids degassed from the deeper levels of the MBI can explain the high Pd/Pt and Pd/Ir ratios of the deposit. A model is presented in which disseminated Pd-rich sulfide are initially introduced by a high temperature magmatic fluid that also influenced crystallization to produce the gross modal variations of the igneous host rock. This high temperature mineralization event was subsequently modified by the influx of late igneous and country fluids at amphibolite to greenschist conditions.

  18. Apatite (U-Th)/He signal of large-magnitude accelerated glacial erosion, southwest British Columbia

    NASA Astrophysics Data System (ADS)

    Ehlers, Todd A.; Farley, Kenneth A.; Rusmore, Margaret E.; Woodsworth, Glenn J.

    2006-09-01

    Alpine glaciers are efficient agents of erosion and capable of significantly modifying topography. Despite recent advances in theoretical and field studies that quantify glacial erosion processes, few studies have documented glacial erosion rates over long (>106 yr) or large (more than tens of kilometers) scales. We use apatite (U-Th)/He (AHe) and apatite fission track (AFT) cooling ages to address the late Miocene to Holocene erosion history across two 60-km-long transects of the heavily glaciated southern Coast Mountains, British Columbia. Observed AHe cooling ages from equal elevation samples range between 1.5 and 8 Ma and suggest that thick alpine glaciers resulted in a 16 km shift of the highest point in the topography in the past 1.5 4.0 m.y. We evaluated temporal and spatial variations in erosion rates using a three-dimensional thermal-kinematic model that predicted AHe and AFT ages at the surface for different erosion histories. Comparison of model predicted and observed cooling ages suggests an increase in erosion rates of as much as 300% over the past 1.5 7 m.y., coincident with the onset of glaciation of this range.

  19. A first report of hydroxylated apatite as structural biomineral in Loasaceae – plants’ teeth against herbivores

    PubMed Central

    Ensikat, Hans-Jürgen; Geisler, Thorsten; Weigend, Maximilian

    2016-01-01

    Biomineralization provides living organisms with various materials for the formation of resilient structures. Calcium phosphate is the main component of teeth and bones in vertebrates, whereas especially silica serves for the protection against herbivores on many plant surfaces. Functional calcium phosphate structures are well-known from the animal kingdom, but had not so far been reported from higher plants. Here, we document the occurrence of calcium phosphate biomineralization in the South-American plant group Loasaceae (rock nettle family), which have stinging trichomes similar to those of the well-known stinging nettles (Urtica). Stinging hairs and the smaller, glochidiate trichomes contained nanocrystalline hydroxylated apatite, especially in their distal portions, replacing the silica found in analogous structures of other flowering plants. This could be demonstrated by chemical, spectroscopic, and diffraction analyses. Some species of Loasaceae contained both calcium phosphate and silica in addition to calcium carbonate. The intriguing discovery of structural hydroxylated apatite in plants invites further studies, e.g., on its systematic distribution across the family, the genetic and cellular control of plant biomineralization, the properties and ultrastructure of calcium phosphate. It may prove the starting point for the development of biomimetic calcium phosphate composites based on a cellulose matrix. PMID:27194462

  20. Interstitial Oxide Ion Distribution and Transport Mechanism in Aluminum-Doped Neodymium Silicate Apatite Electrolytes.

    PubMed

    An, Tao; Baikie, Tom; Orera, Alodia; Piltz, Ross O; Meven, Martin; Slater, Peter R; Wei, Jun; Sanjuán, María L; White, T J

    2016-04-01

    Rare earth silicate apatites are one-dimensional channel structures that show potential as electrolytes for solid oxide fuel cells (SOFC) due to their high ionic conductivity at intermediate temperatures (500-700 °C). This advantageous property can be attributed to the presence of both interstitial oxygen and cation vacancies, that create diffusion paths which computational studies suggest are less tortuous and have lower activation energies for migration than in stoichiometric compounds. In this work, neutron diffraction of Nd(28+x)/3AlxSi6-xO26 (0 ≤ x ≤ 1.5) single crystals identified the locations of oxygen interstitials, and allowed the deduction of a dual-path conduction mechanism that is a natural extension of the single-path sinusoidal channel trajectory arrived at through computation. This discovery provides the most thorough understanding of the O(2-) transport mechanism along the channels to date, clarifies the mode of interchannel motion, and presents a complete picture of O(2-) percolation through apatite. Previously reported crystallographic and conductivity measurements are re-examined in the light of these new findings. PMID:27015162

  1. Microwave assisted apatite coating deposition on Ti6Al4V implants.

    PubMed

    Zhou, Huan; Nabiyouni, Maryam; Bhaduri, Sarit B

    2013-10-01

    In this work we report a novel microwave assisted technology to deposit a uniform, ultra-thin apatite coating without any cracks on titanium implants in minutes. This method comprises of conventional biomimetic coating in synergism with microwave irradiation to result in alkaline earth phosphate nucleation. The microwave assisted coating process mainly follows the initial stages of biomimetic coating until the step of the Ca-P nuclei formation. After that, due to microwave irradiation more Ca-P nuclei are formed to cover the whole surface of the implant instead of the growth of deposited Ca-P nuclei to Ca-P globules and coatings. It is interesting to note the doping of Mg(2+) to Ca-P apatite coating can significantly change the properties and performances of as-deposited coatings. The hydrophilicity, physical properties, bioactivity, cell adhesion, and growth capability of as-deposited microwave assisted coatings were investigated. The study shows that this coating technology has great potential in biomedical applications. Additionally, since biomimetic coating can be applied to series of implant materials such as polymer, metals and glass, it is expected this microwave assisted coating technology can also be applied to these materials if they can remains stable at 100 °C, the boiling point of water. PMID:23910363

  2. Highly porous polymer-derived wollastonite-hydroxycarbonate apatite ceramics for bone regeneration.

    PubMed

    Fiocco, L; Li, S; Bernardo, E; Stevens, M M; Jones, J R

    2016-04-01

    A novel strategy was employed to synthesize highly porous wollastonite-hydroxycarbonate apatite ceramic scaffolds for bone regeneration. A commercial liquid preceramic polymer filled with micro-CaCO3 powders was foamed at low temperature (at 350 °C), using the decomposition of a hydrazine additive, and then converted into ceramic by a treatment at 700 °C. Hydroxycarbonate apatite was later developed by a phosphatization treatment of ceramized foams, in a P-rich solution, while wollastonite was obtained by a second firing, at 900 °C. The effectiveness of the method was proven by x-ray diffraction analysis, showing the presence of the two expected crystalline phases. Porosity, interconnect size distribution and mechanical strength were in the range that is thought to be suitable for bone regeneration in non-load bearing sites (compressive strength ≈ 3 MPa, porosity ≈ 90%, modal interconnect diameter ≈ 130-160 μm). In addition, bioactivity and ion release rate were assessed in simulated body fluid (SBF). MC3T3 osteoblast precursor cells were able to colonize the material in vitro through the pore architecture and expressed osteogenic markers. PMID:27066770

  3. Histological Comparison in Rats between Carbonate Apatite Fabricated from Gypsum and Sintered Hydroxyapatite on Bone Remodeling.

    PubMed

    Ayukawa, Yasunori; Suzuki, Yumiko; Tsuru, Kanji; Koyano, Kiyoshi; Ishikawa, Kunio

    2015-01-01

    Carbonate apatite (CO3Ap), the form of apatite found in bone, has recently attracted attention. The purpose of the present study was to histologically evaluate the tissue/cellular response toward the low-crystalline CO3Ap fabricated using a dissolution-precipitation reaction with set gypsum as a precursor. When set gypsum was immersed in a 100°C 1 mol/L Na3PO4 aqueous solution for 24 h, the set gypsum transformed into CO3Ap. Both CO3Ap and sintered hydroxyapatite (s-HAp), which was used as a control, were implanted into surgically created tibial bone defects of rats for histological evaluation. Two and 4 weeks after the implantation, histological sections were created and observed using light microscopy. The CO3Ap granules revealed both direct apposition of the bone matrix by osteoblasts and osteoclastic resorption. In contrast, the s-HAp granules maintained their contour even after 4 weeks following implantation which implied that there was a lack of replacement into the bone. The s-HAp granules were sometimes encapsulated with fibrous tissue, and macrophage polykaryon was occasionally observed directly apposed to the implanted granules. From the viewpoint of bone remodeling, the CO3Ap granules mimicked the bone matrix, suggesting that CO3Ap may be an appropriate bone substitute. PMID:26504813

  4. Sorption behavior of Zn(II) ions on synthetic apatitic calcium phosphates

    NASA Astrophysics Data System (ADS)

    Sebei, Haroun; Pham Minh, Doan; Nzihou, Ange; Sharrock, Patrick

    2015-12-01

    The synthesis, characterization and the reactivity of apatitic calcium phosphates (Ca-HA, chemical formula Ca10(PO4)6(OH)2) is reported. Calcium carbonate (CaCO3) and potassium dihydrogen orthophosphate (KH2PO4) were selected as economical starting materials for the synthesis of Ca-HA under atmospheric conditions. Monocalcium phosphate monohydrate (MCPM), dicalcium phosphate dihydrate (DCPD), and octacalcium phosphate pentahydrate (OCP) were identified as the main intermediates of the synthesis reaction. The product obtained after 48 h of reaction contains mainly low-crystalline Ca-HA and small amounts of other calcium phosphates such as octacalcium phosphate (OCP), B-type carbonate apatite (CAP), as well as unreacted calcium carbonate. This Ca-HA was found to be active for the removal of Zn2+ from an aqueous solution. Its sorption capacity reached up to 120 mg of Zn2+ per g of Ca-HA powder after 24 h of reaction. The monitoring of soluble Zn, Ca and P during the sorption experiment allowed characterizing the mechanism of Zn uptake. Dissolution-precipitation, ionic exchange and surface complexation are the three main mechanisms involved in the sorption processes. The contribution of these mechanisms is discussed in detail.

  5. Synthesis and characterization of nanocrystalline apatites from solution modeling human blood

    NASA Astrophysics Data System (ADS)

    Solodyankina, Anna; Nikolaev, Anton; Frank-Kamenetskaya, Olga; Golovanova, Olga

    2016-09-01

    Present paper is devoted to the research of the calcification processes in the blood plasma of human body. Spontaneous crystallization from the solution modeling the inorganic part of the blood plasma has been carried out. Obtained precipitates were studied by the various instrumental methods (X-ray powder diffraction, Fourier-transformed infrared spectroscopy, scanning electron microscopy, electron probe microanalysis and gas-volumetric method). All gathered data allow to summarize that nonstoichiometric carbonated hydroxyapatite with low crystallinity (CSD lengths 18-28 nm), high water content and small amount of chlorine ion was obtained throughout the syntheses. Part of vacancies at the Ca sites varies from 0.17 to 0.87; the value of the Cat/(P + C) ratio-from 1.52 to 1.64 (where Cat = Ca2+ + Na+ + K+ + Mg2+). The poor crystallized synthetic apatites with high carbonate ion content (from 4.34 to 5.54 wt%) and c parameter (6.888-6.894 Å) are analogues of the apatites of the pathological cardiovascular deposits. They can be obtained from the solution modeling human blood plasma by the inorganic components with calcium phosphate supersaturation 25 and 50 and with 10 and 12 weeks experiment time.

  6. The role of intracellular calcium phosphate in osteoblast-mediated bone apatite formation

    PubMed Central

    Boonrungsiman, Suwimon; Gentleman, Eileen; Carzaniga, Raffaella; Evans, Nicholas D.; McComb, David W.; Porter, Alexandra E.; Stevens, Molly M.

    2012-01-01

    Mineralization is a ubiquitous process in the animal kingdom and is fundamental to human development and health. Dysfunctional or aberrant mineralization leads to a variety of medical problems, and so an understanding of these processes is essential to their mitigation. Osteoblasts create the nano-composite structure of bone by secreting a collagenous extracellular matrix (ECM) on which apatite crystals subsequently form. However, despite their requisite function in building bone and decades of observations describing intracellular calcium phosphate, the precise role osteoblasts play in mediating bone apatite formation remains largely unknown. To better understand the relationship between intracellular and extracellular mineralization, we combined a sample-preparation method that simultaneously preserved mineral, ions, and ECM with nano-analytical electron microscopy techniques to examine osteoblasts in an in vitro model of bone formation. We identified calcium phosphate both within osteoblast mitochondrial granules and intracellular vesicles that transported material to the ECM. Moreover, we observed calcium-containing vesicles conjoining mitochondria, which also contained calcium, suggesting a storage and transport mechanism. Our observations further highlight the important relationship between intracellular calcium phosphate in osteoblasts and their role in mineralizing the ECM. These observations may have important implications in deciphering both how normal bone forms and in understanding pathological mineralization. PMID:22879397

  7. Flotation selectivity of novel alkyl dicarboxylate reagents for apatite-calcite separation.

    PubMed

    Karlkvist, Tommy; Patra, Anuttam; Rao, Kota Hanumantha; Bordes, Romain; Holmberg, Krister

    2015-05-01

    The investigation aims to demonstrate the conceptual thoughts behind developing mineral specific reagents for use in flotation of calcium containing ores. For this purpose, a series of dicarboxylate-based surfactants with varying distance between the carboxylate groups (one, two or three methylene groups) was synthesized. A surfactant with the same alkyl chain length but with only one carboxylate group was also synthesized and evaluated. The adsorption behavior of these new reagents on pure apatite and pure calcite surfaces was studied using Hallimond tube flotation, FTIR and ζ potential measurements. The relation between the adsorption behavior of a given surfactant at a specific mineral surface and its molecular structure over a range of concentrations and pH values, as well as the region of maximum recovery, was established. It was found that one of the reagents, with a specific distance between the carboxylate groups, was much more selective for a particular mineral surface than the other homologues. For example, out of the four compounds synthesized, only the one where the carboxylate groups were separated by a single methylene group floated apatite but not calcite, whereas calcite was efficiently floated with the monocarboxylic reagent, but not with the other reagents synthesized. This selective adsorption of a given surfactant to a particular mineral surface relative to other mineral surfaces as evidenced in the flotation studies was substantiated by ζ potential and infra-red spectroscopy data. PMID:25596367

  8. Electrodeposited apatite coating for solid-phase microextraction and sensitive indirect voltammetric determination of fluoride ions.

    PubMed

    Mao, Yuehong; Chen, Yufei; Chu, Lin; Zhang, Xiaoli

    2013-10-15

    Electrodeposition was used to prepare a new solid phase microextraction (SPME) coatings. Two apatite SPME coatings, dicalcium phosphate dihydrate (DCPD or brushite) and hydroxyapatite (HAP) were validly and homogeneously one-step electrodeposited on glassy carbon electrode (GCE) under different conditions. The coatings were characterized by XRD, FTIR, SEM, CV and EIS. The apatite SPME coatings showed excellent and selective adsorbability to fluoride ions. A novel indirect voltammetric strategy for sensitive detection of fluoride was proposed using K3Fe(CN)6 as indicating probe. The detection principle of fluoride ions was based on the increment of steric hindrance after fluoride adsorption, which resulting in the decrease of the amperometric signal to Fe(CN)6(3-). The liner ranges were 0.5-20.0 μmol/L for n-DCPD/GCE with the limit of detection of 0.14 μmol/L and 0.1-50.0 μmol/L for n-HAP/GCE with the limit of detection of 0.069 μmol/L, respectively. The developed method was applied to the analysis of water samples (lake, spring and tap water) and the recovery values were found to be in the range of 90-106%. PMID:24054624

  9. Surface treatment, corrosion behavior, and apatite-forming ability of Ti-45Nb implant alloy.

    PubMed

    Gostin, Petre F; Helth, Arne; Voss, Andrea; Sueptitz, Ralph; Calin, Mariana; Eckert, Jürgen; Gebert, Annett

    2013-02-01

    The low modulus β-type Ti-45Nb alloy is a promising new implant alloy due to its excellent mechanical biocompatibility and composition of non-toxic elements. The effect of surface treatments on the evolution of controlled topography and roughness was investigated by means of scanning electron microscopy and optical profilometry. Severe mechanical treatments, for example sand-blasting, or etching treatments in strongly oxidizing acidic solutions, like HF:HNO(3) (4:1) or H(2)SO(4):H(2)O(2) (1:1) piranha solution were found to be very effective. In particular, the latter generates a nanopatterned surface topography which is expected to be promising for the stimulation of bone tissue growth. Compared to Ti and Ti-6Al-4V, the β-type Ti-45Nb alloy requires significantly longer etching durations due to the high chemical stability of Nb. Severe surface treatments alter the passive film properties, but do not deteriorate the outstanding corrosion resistance of the Ti-45Nb alloy in synthetic body fluid environments. The Ti-45Nb appears to have a lower apatite-formation ability compared to Ti. Etching with H(2)SO(4):H(2)O(2) (1:1) piranha solution inhibits apatite formation on Ti, but not on Ti-45Nb. PMID:23166048

  10. Involvement of 3D osteoblast migration and bone apatite during in vitro early osteocytogenesis.

    PubMed

    Robin, Marc; Almeida, Claudia; Azaïs, Thierry; Haye, Bernard; Illoul, Corinne; Lesieur, Julie; Giraud-Guille, Marie-Madeleine; Nassif, Nadine; Hélary, Christophe

    2016-07-01

    The transition from osteoblast to osteocyte is described to occur through passive entrapment mechanism (self-buried, or embedded by neighboring cells). Here, we provide evidence of a new pathway where osteoblasts are "more" active than generally assumed. We demonstrate that osteoblasts possess the ability to migrate and differentiate into early osteocytes inside dense collagen matrices. This step involves MMP-13 simultaneously with IBSP and DMP1 expression. We also show that osteoblast migration is enhanced by the presence of apatite bone mineral. To reach this conclusion, we used an in vitro hybrid model based on both the structural characteristics of the osteoid tissue (including its density, texture and three-dimensional order), and the use of bone-like apatite. This finding highlights the mutual dynamic influence of osteoblast cell and bone extra cellular matrix. Such interactivity extends the role of physicochemical effects in bone morphogenesis complementing the widely studied molecular signals. This result represents a conceptual advancement in the fundamental understanding of bone formation. PMID:27150828

  11. High-resolution electron microscopy study of synthetic carbonate and aluminum containing apatites.

    PubMed

    Layani, J D; Cuisinier, F J; Steuer, P; Cohen, H; Voegel, J C; Mayer, I

    2000-05-01

    Aluminum (Al)-containing calcium-deficient carbonated hydroxyapatites were produced by a precipitation method from aqueous solution with carbonate (0-6.1%) and aluminum (0.1-0.5%) concentrations close to those found in biological materials. Two series of apatites were prepared: one at pH 7.0 and another at pH 9. 0. High-resolution electron microscopy has shown that many of them possess structural defects such as screw dislocations, grain boundaries, and central defects. Samples with high carbonate content and high water and high Al(3+) content had a high amount of structural defects. Accordingly, a sample (7Al1) with a relatively high carbonate content (6.1%) and a sample (7Al6) without carbonate but with a relatively high water (2.0 mol) and Al(3+) content (0. 39%) presented the highest amount of structural defects, 54% and 47%, respectively. A sample (7Al13) with a low level of crystalline water (1 mol) and low carbonate (2.5%) showed a small amount of defects. The presence of water associated with Al(3+) induced a high number of crystals having a central defect with a great similarity to the so-called water layer of octacalcium phosphate (OCP). Observed images of all these crystals have shown good correspondence with the computer-simulated image based on the crystal structure of hydroxyapatite, indicating that the addition of Al(3+) and carbonate does not perturb the apatitic structure. PMID:10679685

  12. Seawater rare-earth element patterns preserved in apatite of Pennsylvanian conodonts?

    NASA Astrophysics Data System (ADS)

    Bright, Camomilia A.; Cruse, Anna M.; Lyons, Timothy W.; MacLeod, Kenneth G.; Glascock, Michael D.; Ethington, Raymond L.

    2009-03-01

    Past workers have used rare-earth element patterns recorded in biogenic apatite as proxies for original seawater chemistry. To explore the potency of this approach, we analyzed Pennsylvanian conodonts from limestones, gray shales, and black shales of the Fort Scott and Pawnee formations (Desmoinesian) and Swope and Dennis formations (Missourian) in Kansas, Missouri, and Iowa, U.S.A. Analysis of individual platform conodonts from seven taxa using laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) revealed a consistent enrichment in the middle rare-earth elements (MREE). Analogous MREE enrichment has been observed in authigenic apatite and bulk samples of phosphate-rich black shales from the same formations. Importantly, however, phosphate-depleted shales intimately associated with the P-rich intervals are relatively depleted in MREE. These antithetic patterns argue convincingly for secondary migration from the bulk sediment into the phosphate, and the extent of MREE enrichment in the conodonts is correlated positively with the total REE content. MREE enrichment in conodonts does not vary systematically as a function of lithology, stratigraphic level, conodont genus, geographic location, or with independent estimates of paleoredox conditions in the bottom waters. Collectively, these results argue for postmortem (diagenetic) REE uptake resulting in a pronounced (and progressive) MREE enrichment. Any cerium anomalies, if initially present, were masked by diagenetic uptake of REE. Paleoenvironmental interpretations of conodont REE, particularly for samples exhibiting MREE enrichment, should therefore be viewed with caution.

  13. Apatite intergrowths in clinopyroxene megacrysts from the Ostrzyca Proboszczowicka (SW Poland) basanite

    NASA Astrophysics Data System (ADS)

    Lipa, Danuta; Puziewicz, Jacek; Ntaflos, Theodoros; Matusiak-Małek, Magdalena

    2015-04-01

    The Cenozoic basanite from the Ostrzyca Proboszczowicka in Lower Silesia (SW Poland) belongs to numerous lavas occurring in the NE part of the Central European Volcanic Province. Basanite contains clinopyroxene megacrysts up to 3 cm in size. The clinopyroxene has the composition of aluminian-sodian diopside (mg# 0.61-0.70, 0.08-0.12 atoms Na pfu and 0.88-0.93 atoms Ca pfu). Cr is absent. The REE contents are above the primitive mantle reaching up to 18 x PM at Nd. Primitive-mantle normalized REE patterns show enrichment in LREE relative to HREE (LaN/LuN=3.81-5.01). The REE patterns of all the megacrysts show deflection in La-Nd. The trace element patterns are characterized by positive Zr, Hf and in some cases also Ta anomalies, and negative U, La, Sr, Ti and Pb ones. In some samples strong depletion (down to 0.01 x PM) in Rb and Ba is observed.The Ostrzyca megacrysts formed cumulate, which crystallized from magma similar to the host basanite, but more fractionated and enriched in REE, particularly in LREE (Lipa et al., 2014). This happened at mid-crustal depths (10-15 km) and the new pulse of basanitic magma entrained the crystals forming the non-solidified cumulate and brought them to the surface (Lipa et al., 2014). Clinopyroxene megacrysts contain large, transparent, euhedral apatite crystals up to 7 mm. The major element composition indicates the fluor-apatite with F content ranging from 0.87 to 1.93 wt.%. Chlorine content is strongly variable between grains (0.05-1.75 wt.%). Apatite is strongly enriched in LREE relative to HREE (LaN/LuN=60.39-62.23, about 1000 x PM for LREE and about 10 x PM for HREE). The REE patterns are nearly linear, with slight positive Nd and Gd anomalies. The trace element patterns are characterized by very strong negative anomalies of HFSE (Nb, Ta, Zr, Hf, Ti) and Pb, and weaker negative Sr anomaly. Concentration of Yb and Lu is on the level 10 x PM, whereas Rb, Hf and Ti are depleted relative to PM. Apatite preceded clinopyroxene

  14. SUPERFUND TREATABILITY CLEARINGHOUSE: FULL SCALE ROTARY KILN INCINERATOR FIELD TRIAL: PHASE I, VERIFICATION TRIAL BURN ON DIOXIN/HERBICIDE ORANGE CONTAMINATED SOIL

    EPA Science Inventory

    This treatability study reports on the results of one of a series of field trials using various remedial action technologies that may be capable of restoring Herbicide Orange (HO)XDioxin contaminated sites. A full-scale field trial using a rotary kiln incinerator capable of pro...

  15. Nanocrystalline carbonate-apatites: role of Ca/P ratio on the upload and release of anticancer platinum bisphosphonates

    NASA Astrophysics Data System (ADS)

    Iafisco, Michele; Palazzo, Barbara; Martra, Gianmario; Margiotta, Nicola; Piccinonna, Sara; Natile, Giovanni; Gandin, Valentina; Marzano, Cristina; Roveri, Norberto

    2011-12-01

    In the present study two nanocrystalline apatites have been investigated as bone-specific drug delivery devices to be used for treatment of bone tumors either by local implantation or by injection. In order to assess how the Ca/P ratio can influence the adsorption and release of anticancer platinum-bisphosphonate complexes, two kinds of apatite nanocrystals having different Ca/P ratios but similar morphologies, degree of crystallinity, and surface areas have been synthesized and characterized. The two platinum-bisphosphonate complexes considered were the bis-{ethylenediamineplatinum(ii)}-2-amino-1-hydroxyethane-1,1-diyl-bisphosphonate and the bis-{ethylenediamineplatinum(ii)}medronate. The Ca/P ratio plays an important role in the adsorption as well as in the release of the two drugs. In fact, the apatite with a higher Ca/P ratio showed greater affinity for both platinum complexes. Also the chemical structure of the two Pt complexes appreciably affects their affinity towards as well as their release from the two kinds of apatites. In particular, the platinum complex whose bisphosphonate contains a free aminic group showed greater upload and smaller release. The cytotoxicity of the Pt complexes released from the apatite was tested against human cervical, colon, and lung cancer cells as well as against osteosarcoma cells. In agreement with previous work, the Pt complexes released were found to be more cytotoxic than the unmodified complexes.In the present study two nanocrystalline apatites have been investigated as bone-specific drug delivery devices to be used for treatment of bone tumors either by local implantation or by injection. In order to assess how the Ca/P ratio can influence the adsorption and release of anticancer platinum-bisphosphonate complexes, two kinds of apatite nanocrystals having different Ca/P ratios but similar morphologies, degree of crystallinity, and surface areas have been synthesized and characterized. The two platinum

  16. Experimental Determination of Hydrogen Partitioning in an Apatite-Haplobasalt Andesite Melt System at 1200°C and 1 GPa

    NASA Astrophysics Data System (ADS)

    Huh, M. C.; Boyce, J.; Manning, C. E.; Medard, E.

    2011-12-01

    Igneous apatite crystals contain a record of the evolving concentrations of magmatic volatile elements such as F, H, and Cl during crystallization and degassing. In order to develop apatite as a quantitative barometer of magmatic volatile species, improved understanding of apatite-melt volatile equilibria is needed. We conducted apatite crystallization experiments using a piston cylinder apparatus at 1,200°C and 1 GPa. Apatite crystals were grown from an Fe- and Cl-free, haplobasaltic-andesite melt of constant composition. Experiments were quenched to below 700°C in 15 seconds, producing homogeneous glass plus apatite crystals ranging from 5 to 30 microns in diameter. Apatite and coexisting glass were analyzed using the Cameca ims 6f SIMS, with an O- beam and positive secondary ions, following the methods of Boyce and Hervig (2008, 2009), but using the inversion-based calibration routines of Boyce and Eiler (this meeting). These measurements provide the first direct constraint on the partitioning of hydrogen between apatite and melt. For the exchange reaction F-(melt) + OHapatite = OH-(melt) + Fapatite, the Keq was calculated from the measured data to be ~25, consistent with the results of Mathez and Webster (2004) and Webster et al. (2008), despite our experiments being nominally Cl- and Fe-free. Significant non-Henrian behavior is observed for hydrogen, but trace F behaves effectively Henrian at low concentrations, again consistent with previous work. These preliminary results reinforce the assertion that simple Henry's or Raoult's Law models of volatile partitioning between apatite and melt are rarely - if ever - appropriate, and that both F and H concentrations must be considered in order to use hydrogen concentrations in apatite to determine concentrations of hydrogen in the coexisting melt.

  17. Oxygen isotope fractionation between apatite-bound carbonate and water determined from controlled experiments with synthetic apatites precipitated at 10-37 °C

    NASA Astrophysics Data System (ADS)

    Lécuyer, Christophe; Balter, Vincent; Martineau, François; Fourel, François; Bernard, Aurélien; Amiot, Romain; Gardien, Véronique; Otero, Olga; Legendre, Serge; Panczer, Gérard; Simon, Laurent; Martini, Rossana

    2010-04-01

    The oxygen isotope fractionation between the structural carbonate of inorganically precipitated hydroxyapatite (HAP) and water was determined in the range 10-37 °C. Values of 1000 ln α( CO32--HO) are linearly correlated with inverse temperature (K) according to the following equation: 1000 ln α( CO32--HO) = 25.19 (±0.53)· T-1 - 56.47 (±1.81) ( R2 = 0.998). This fractionation equation has a slightly steeper slope than those already established between calcite and water ( O'Neil et al., 1969; Kim and O'Neil, 1997) even though measured fractionations are of comparable amplitude in the temperature range of these experimental studies. It is consequently observed that the oxygen isotope fractionation between apatite carbonate and phosphate increases from about 7.5‰ up to 9.1‰ with decreasing temperature from 37 °C to 10 °C. A compilation of δ 18O values of both phosphate and carbonate from modern mammal teeth and bones confirms that both variables are linearly correlated, despite a significant scattering up to 3.5‰, with a slope close to 1 and an intercept corresponding to a 1000 ln α( CO32--PO43-) value of 8.1‰. This apparent fractionation factor is slightly higher or close to the fractionation factor expected to be in the range 7-8‰ at the body temperature of mammals.

  18. Combined apatite fission-track and single grain apatite (U Th)/He ages from basement rocks of central Dronning Maud Land (East Antarctica) — Possible identification of thermally overprinted crustal segments?

    NASA Astrophysics Data System (ADS)

    Emmel, B.; Jacobs, J.; Crowhurst, P.; Daszinnies, M. C.

    2007-12-01

    Apatite fission-track (FT) and single grain (U-Th)/He ages from four vertical profiles in central Dronning Maud Land (East Antarctica) range from 312 ± 20 Ma to 135 ± 11 Ma and 304 ± 28 Ma to 104 ± 8 Ma, respectively. The combined age data allows to discriminate between undisturbed cooled (due to exhumation) and thermally overprinted crustal blocks. Profiles at the Zwieselhöhe and the Conradgebirge revealed unusual apatite FT vs. elevation relationships and (U-Th)/He ages older than the corresponding central apatite FT ages, possibly providing evidence for a Jurassic thermal overprint. Most probably Jurassic magmatism and associated advective heating led to total annealing of the apatite fission-tracks but helium only partially diffused. The model developed in this paper suggests that the (U-Th)/He ages from the Zwieselhöhe and Conradgebirge profiles are in part relicts of the pre-Jurassic cooling history. Two thermally undisturbed vertical profiles are used to record the long-term cooling history of central Dronning Maud Land. Time-temperature paths derived from modelled apatite FT data of these profiles revealed two phases of accelerated cooling during the Late Carboniferous and the Early Jurassic. Both phases are followed by slow cooling which is also documented by the spread in apatite (U-Th)/He single grain ages. The cooling at the end of the Carboniferous is most probably related to far field effects associated to the prevailing convergent tectonics. During the initial separation between East Antarctica and Mozambique erosion along an evolving rift shoulder caused the Jurassic cooling. Denudation of the basement was simultaneous with volcanism with both pre-dating (c. 20-10 Ma) sea-floor spreading in the Riser Larsen Sea (c. 155 Ma). Post Jurassic cooling was restricted to the lowest temperature sensitivity of both methods. Combined inverse modelled apatite FT data and forward modelled (U-Th)/He data suggest an Eocene/Oligocene cooling step, possibly

  19. How Many Have Died from Undiagnosed Human Immunodeficiency Virus–Associated Histoplasmosis, A Treatable Disease? Time to Act

    PubMed Central

    Nacher, Mathieu; Adenis, Antoine; Aznar, Christine; Blanchet, Denis; Vantilcke, Vincent; Demar, Magalie; Carme, Bernard; Couppié, Pierre

    2014-01-01

    Human immunodeficiency virus (HIV)–associated disseminated Histoplasma capsulatum capsulatum infection often mimics tuberculosis. This disease is well know in the United States but is dramatically underdiagnosed in Central and South America. In the Amazon region, given the available incidence data and the regional HIV prevalence, it is expected that, every year, 1,500 cases of histoplasmosis affect HIV patients in that region alone. Given the mortality in undiagnosed patients, at least 600 patients would be expected to die from an undiagnosed but treatable disease. The lack of a simple diagnostic tool and the lack of awareness by clinicians spiral in a vicious cycle and made a major problem invisible for 30 years. The HIV/acquired immunodeficiency syndrome community should tackle this problem now to prevent numerous avoidable deaths from HIV-associated histoplasmosis in the region and elsewhere. PMID:24277783

  20. How many have died from undiagnosed human immunodeficiency virus-associated histoplasmosis, a treatable disease? Time to act.

    PubMed

    Nacher, Mathieu; Adenis, Antoine; Aznar, Christine; Blanchet, Denis; Vantilcke, Vincent; Demar, Magalie; Carme, Bernard; Couppié, Pierre

    2014-02-01

    Human immunodeficiency virus (HIV)-associated disseminated Histoplasma capsulatum capsulatum infection often mimics tuberculosis. This disease is well know in the United States but is dramatically underdiagnosed in Central and South America. In the Amazon region, given the available incidence data and the regional HIV prevalence, it is expected that, every year, 1,500 cases of histoplasmosis affect HIV patients in that region alone. Given the mortality in undiagnosed patients, at least 600 patients would be expected to die from an undiagnosed but treatable disease. The lack of a simple diagnostic tool and the lack of awareness by clinicians spiral in a vicious cycle and made a major problem invisible for 30 years. The HIV/acquired immunodeficiency syndrome community should tackle this problem now to prevent numerous avoidable deaths from HIV-associated histoplasmosis in the region and elsewhere. PMID:24277783

  1. A laboratory treatability study on RDX-contaminated soil from the Iowa Army Ammunition Plant, Burlington, Iowa.

    SciTech Connect

    Boopathy, R.; Manning, J. F.; Environmental Research

    2000-03-01

    Soil in certain areas of the Iowa Army Ammunition Plant in Burlington, Iowa, was contaminated with hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX). A laboratory treatability study was conducted to examine the ability of native soil bacteria present in the contaminated site to degrade RDX. The results indicated that RDX can be removed effectively from the soil by native soil bacteria through a co-metabolic process. Molasses, identified as an effective cosubstrate, is inexpensive, and this factor makes the treatment system cost effective. The successful operation of aerobic-anoxic soil-slurry reactors in batch mode with RDX-contaminated soil showed that the technology can be scaled up for field demonstration. The RDX concentration in the contaminated soil was decreased by 98% after 4 months of reactor operation. The advantage of the slurry reactor is the simplicity of its operation. The method needs only mixing and the addition of molasses as cosubstrate.

  2. REE Mineralization in Kiruna-type Magnetite-Apatite Ore Deposits: Magmatism and Metasomatism

    NASA Astrophysics Data System (ADS)

    Harlov, D. E.

    2015-12-01

    Magnetite-apatite ore bodies of the Kiruna type occur worldwide and are generally associated with volcanic rocks or volcanism. They also show strong evidence of extensive metasomatism over a wide P-T range. Notable examples include the Kiirunavaara ore body, northern Sweden (Harlov et al., 2002, Chem. Geol., 191, 47-72); the Grängesberg ore body, central Sweden (Jonsson et al., 2010, NGF abstracts, vol 1, 88-89); the Mineville ore body, Adirondacks, New York, USA (McKeown and Klemc, 1956, U.S. Geol Sur Bull (1956), pp. 9-23); the Pea Ridge ore body, SE Missouri, USA (Kerr, 1998, MS Thesis, Univ. Windsor, Windsor, Ontario, Canada 113 pp); the Jurassic Marcona ore body in south-central Peru (Chen et al., 2010, Econ Geol, 105, 1441-1456); and a collection of ore bodies from the Bafq Region, central Iran (Daliran et al., 2010, Geol. Assoc. Canada, Short Course Notes, v. 20, p.147-159). In these ore bodies, low Th and U monazite, xenotime, allanite, REE carbonates, and/or REE fluorides are commonly associated with the apatite as inclusions, rim grains, or as independent grains in the surrounding mineral matrix. High contrast BSE imaging, coupled with EMPA and LA-ICPMS, indicates that the apatite has experienced fluid-induced alteration in the form of (Y+REE) + Na + Si + Cl depletion implying that it served as the source for the (Y+REE) (e.g. Kiirunavaara, northern Sweden; Harlov et al., 2002). Formation of monazite and xenotime associated with fluorapatite, as inclusions or rim grains, has experimentally been demonstrated to originate from the fluorapatite as the result of fluid-aided, coupled dissolution-reprecipitation processes (Harlov et al., 2005, Contrib. Mineral. Petrol. 150, 268-286). This is explains the low Th and U content of the monazite and xenotime. Fluid sources could range from 700-900 °C, residual, acidic (HCl, H2HSO4) grain boundary fluids, remaining after the last stages of ore body crystallization, to later stage, cooler (< 600 °C) (H2O-CO2-(Na

  3. Investigation of the stability of Co-doped apatite ionic conductors in NH{sub 3}

    SciTech Connect

    Headspith, D.A.; Orera, A.; Young, N.A.; Francesconi, M.G.

    2010-12-15

    Hydrogen powered solid oxide fuel cells (SOFCs) are of enormous interest as devices for the efficient and clean production of electrical energy. However, a number of problems linked to hydrogen production, storage and transportation are slowing down the larger scale use of SOFCs. Identifying alternative fuel sources to act as intermediate during the transition to the full use of hydrogen is, therefore, of importance. One excellent alternative is ammonia, which is produced on a large scale, is relatively cheap and has the infrastructure for storage and transportation already in place. However, considering that SOFCs operate at temperatures higher than 500 {sup o}C, a potential problem is the interaction of gaseous ammonia with the materials in the cathode, anode and solid electrolyte. In this paper, we extend earlier work on high temperature reactions of apatite electrolytes with NH{sub 3} to the transition metal (Co) doped systems, La{sub 9.67}Si{sub 5}CoO{sub 26} and La{sub 10}(Si/Ge){sub 5}CoO{sub 26.5}. A combination of PXRD, TGA and XAFS spectroscopy data showed a better structural stability for the silicate systems. Apatite silicates and germanates not containing transition metals tend to substitute nitride anions for their interstitial oxide anions, when reacted with NH{sub 3} at high temperature and, consequentially, lower the interstitial oxide content. In La{sub 9.67}Si{sub 5}CoO{sub 26} and La{sub 10}(Si/Ge){sub 5}CoO{sub 26.5} reduction of Co occurs as a competing process, favouring lower levels of nitride-oxide substitution. -- Graphical Abstract: In reactions between the apatites La{sub 9.67}Si{sub 5}CoO{sub 26} and La{sub 10}(Si/Ge){sub 5}CoO{sub 26.5} and NH{sub 3} (g) at temperatures T>500 {sup o}C, the partial substitution of the Si and Ge by Co seems to discourage O{sup 2-}/N{sup 3-} substitution in favour of the reduction of the metal. Display Omitted

  4. Volatile budget of Tenerife phonolites inferred from combined haüyne-apatite mineral records

    NASA Astrophysics Data System (ADS)

    Cooper, Lauren B.; Bachmann, Olivier; Huber, Christian

    2015-04-01

    Intermediate to silicic volcanic eruptions often emit more S than predicted by petrological models -- this is called the "excess S problem." While most common minerals in these magmas are poor in volatile elements, the occurrence of large phenocrysts of S-rich haüyne (up to ~13 wt% SO3) in phonolites holds much promise for better constraining volcanic volatile budgets in differentiated alkaline magmatic systems. We have examined textural zonation patterns in haüyne separates from Tenerife (Spain), using mineral oil to enhance grain transparency. Included phases were characterized by energy dispersive spectroscopy, X-ray maps, and Raman spectroscopy. Slow growth of haüyne, inferred from zones with few inclusions, likely represents cooling-induced crystallization from S-rich melt during storage in the upper crust. By contrast, rapid growth of phenocrystic haüyne, generating "wispy" zones containing Fe-rich haüyne laths and zones rich in melt inclusions, fluid inclusions, and Fe-sulfide inclusions, may be associated with magma recharge and/or upward percolation of a low-density fluid phase (i.e., "gas sparging"). Both processes could bring new pulses of S from deep within the magmatic system. Zones containing thousands of fluid inclusions provide direct physical evidence that the melt was fluid-saturated during periods of rapid haüyne growth. Transfer of S-rich fluid should occur in all volatile-rich magmatic systems, including dacitic-rhyolitic arc systems with large S excesses, but is difficult to document in such magmas devoid of a large S-rich mineral phase like haüyne. Apatite, a mineral present in all volcanic rocks, may also contain information about S. We have observed intricate chemical zonation in backscattered electron images of apatite microphenocrysts from the same Tenerife samples. Variations in volatile and trace element concentrations between successive zones (measured via wavelength dispersive spectroscopy and laser ablation-inductively coupled

  5. The Kiruna-type apatite-iron oxide system in central Sweden: geology and geochemical character

    NASA Astrophysics Data System (ADS)

    Högdahl, K.; Jonsson, E.; Nilsson, K.; Troll, V.

    2012-04-01

    The only apatite-iron oxide ores in the classic Palaeoproterozoic Bergslagen ore province, central Sweden, occur semi-continuously between Grängesberg and Idkerberget. Together, they represent the largest concentration of iron ore in this part of the Fennoscandian shield. Their mineralogy, geochemistry, geometry and host rock relations all suggest that they belong to the Kiruna-type class of deposits. The apatite-iron oxide ores in Bergslagen are hosted by 1.9 Ga variably altered, metavolcanic to meta-subvolcanic rocks ranging from rhyolitic to andesitic in composition. The region has been affected by three episodes of deformation (D1-3) and regional, greenschist to amphibolite facies metamorphism during the c. 1.9-1.8 Ga Svecokarelian orogeny. The Grängesberg deposits occur as narrow, moderately SE-dipping lenses that are concordant to S0 surfaces in the host rocks. Magnetic anomaly data indicate that they extend to a depth of at least 1.7 km. The lens geometry is mainly controlled by deformation during D2. Reverse, oblique, top-to-the NNW shear is evident in the footwall, and strain partitioning due to competence contrasts between the ore and altered host rocks resulted in flattening at competent ore lens crests, leading to asymmetrical folds with opposite vergence towards pinch areas where prolate strain prevailed. D1 is evident as a crenulated cleavage and D3 appears as gentle, large-scale open folds. Geochemical data on host rocks show a systematic enrichment in REE from the least to the most altered rocks. The ore-associated alteration assemblages and the apatite-iron oxide ore feature similar and elevated REE concentrations and profiles, suggesting a link between hydrothermal alteration and oxide ore formation. However, most ore magnetite has δ18O values between +0.3 and +3.4 ‰ (ranging from -0.4 to +4.9 ‰), consistent with fractionation of oxygen between magnetite and a felsic to intermediate magma at high temperatures (Jonsson et al. 2011). These

  6. Apatite-coated Silk Fibroin Scaffolds to Healing Mandibular Border Defects in Canines

    PubMed Central

    Zhao, Jun; Zhang, Zhiyuan; Wang, Shaoyi; Sun, Xiaojuan; Zhang, Xiuli; Chen, Jake; Kaplan, David L.; Jiang, Xinquan

    2010-01-01

    Tissue engineering has become a new approach for repairing bony defects. Highly porous osteoconductive scaffolds perform the important role for the success of bone regeneration. By biomimetic strategy, apatite-coated porous biomaterial based on silk fibroin scaffolds (SS) might provide an enhanced osteogenic environment for bone-related outcomes. To assess the effects of apatite-coated silk fibroin (mSS) biomaterials for bone healing as a tissue engineered bony scaffold, we explored a tissue engineered bony graft using mSS seeded with osteogenically induced autologous bone marrow stromal cells (bMSCs) to repair inferior mandibular border defects in a canine model. The results were compared with those treated with bMSCs/SS constructs, mSS alone, SS alone, autologous mandibular grafts and untreated blank defects. According to radiographic and histological examination, new bone formation was observed from 4 weeks post-operation, and the defect site was completely repaired after 12 months for the bMSCs/mSS group. In the bMSCs/SS group, new bone formation was observed with more residual silk scaffold remaining at the center of the defect compared with the bMSCs/mSS group. The engineered bone with bMSCs/mSS achieved satisfactory bone mineral densities (BMD) at 12 months post-operation close to those of normal mandible (p>0.05). The quantities of newly formed bone area for the bMSCs/mSS group was higher than the bMSCs/SS group (p<0.01), but no significant differences were found when compared with the autograft group (p>0.05). In contrast, bony defects remained in the center with undegraded silk fibroin scaffold and fibrous connective tissue, and new bone only formed at the periphery in the groups treated with mSS or SS alone. The results suggested apatite-coated silk fibroin scaffolds combined with bMSCs could be successfully used to repair mandibular critical size border defects and the premineralization of these porous silk fibroin protein scaffolds provided an

  7. Apatite-hosted melt inclusions in Damiao massif anorthosite complex, North China

    NASA Astrophysics Data System (ADS)

    Wang, M.; Veksler, I. V.; Zhang, Z.

    2014-12-01

    Models for the nelsonite formation are currently highly contentious, with liquid immiscibility and fractional crystallization as frequently proposed formation mechanisms. The nelsonites in the Damiao massif anorthosite complex in the North China Craton and experimental evidence are revisited for the existence of silica-free CaO-FeO-Fe2O3-TiO2-P2O5 immiscible nelsonitic liquids. Our results of differential scanning calorimetry (DSC) demonstrate that nelsonite with the composition of one-third apatite and two-thirds Fe-Ti oxides by weight completely melts well above 1450 ºC, which is in good agreement with numerous experimental studies of the CaO-P2O5-FexO system in connection to metallurgy. Thus, the composition cannot be molten at temperatures relevant for crystallization of the Damiao magma. A review of experimental studies of liquid immiscibility and analyses of natural immiscible glasses show that all the liquids on the Fe- and P-rich side of the miscibility gap have at least 20 wt. % of aluminosilicate components. Main results of this study come from the analyses of apatite-hosted melt inclusions in Damiao nelsonite. The inclusions range from ~3 to 200 μm in diameter. They are ubiquitous and meet all the morphological criteria of primary melt inclusions crystallised into assemblages of daughter minerals. Almost all of them contain vermiculite and chlorite, and some contain biotite, amphibole, phlogopite and Fe-Ti oxides. Out of dozens analysed inclusions, only three have high contents of SiO2 (62.1-73.8 wt. %) and low contents of FeO (0.25-2.35 wt. %). Bulk compositions of other inclusions show large variations in SiO2 (20.79-50.16 wt. %) and FeOt (13.44-32.78 wt. %). With a few exceptions, the inclusions are very low in CaO (0.04-1.51 wt. %, and high in Al2O3 (10-21.17 wt. %). Despite the high Fe content, the compositions differ from those of the typical immiscible Fe-rich melts. It appears that the cumulus apatite crystallised from Fe-rich, hydrated

  8. Thermal History of Drummond Basin, Queensland (Australia) from Apatite and Zircon (U-Th)/He Thermochronology

    NASA Astrophysics Data System (ADS)

    Zhang, W.; Min, K. K.; Bryan, S. E.

    2014-12-01

    The thermal history of the Drummond Basin in central Queensland (Australia) has only been partly investigated. Inverse thermal modeling of apatite and zircon (U-Th)/He data can reveal the complex thermal history of sedimentary basins. We performed (U-Th)/He dating for detrital apatite and zircon grains extracted from five sandstone samples from the Campaspe DDH-1 drill hole. Mean apatite helium ages generally increase from 65.9 Ma (depth = 538 m) to 83.8 Ma (depth = 263 m). The deeper four samples yielded mean zircon helium (ZHe) ages of 289.7 - 278.2 Ma, with a systematic increase of the ZHe ages from deep to shallow samples. The shallowest sample (depth = 117 m) yielded a mean ZHe age of 263.6 Ma. Our inverse thermal modeling suggests five thermal events since burial: (1) rapid heating to the maximum temperature of 180~380 oC during ~320-290 Ma, (2) rapid cooling from ~260 oC to ~80 oC during ~290-240 Ma, (3) subdued cooling from ~80 oC to ~30 oC during ~240-200 Ma, (4) slow heating from ~30 oC to ~80 oC during ~200-80 Ma, followed by (5) rapid cooling from ~80 oC to ~35 oC at ~80 Ma. The timing and temperature conditions of the initial thermal event are consistent with K/Ar ages and temperatures deduced from illite. This period was characterized by voluminous regional magmatism and crustal extension preceding opening of the overlying Bowen Basin. Rapid cooling during ~290-240 Ma identified by our inverse thermal modeling roughly coincides with the thermal relaxation phase and foreland basin phase of the overlying Bowen Basin. This rapid cooling was probably a result of cessation of extension and subsequent contractional events to the east of Bowen Basin. Cooling slowed down during ~240-200 Ma. The Drummond Basin probably underwent serious erosion during this period, coeval with the peneplanation phase of the Bowen Basin. As is delineated by our modeling, the Drummond Basin was slowly heated from ~20 oC to ~90 oC during ~200-80 Ma, synchronous with development of

  9. Characterization of the bone-like apatite precipitated on high velocity oxy-fuel (HVOF) sprayed calcium phosphate deposits.

    PubMed

    Khor, K A; Li, H; Cheang, P

    2003-02-01

    Bone-like apatite was precipitated on the surface of thermal sprayed calcium phosphate coatings following in vitro incubation in a simulated body fluid. The coatings were initially deposited on titanium alloy substrates by the high velocity oxy-fuel (HVOF) spray technique. Structural characterization and mechanical evaluation of the precipitated apatite layer were conducted. Results showed that the precipitation rate was directly influenced by the local Ca(2+) concentration in the vicinity of the coating's surface and that preferential dissolution of certain phases was found to accelerate the precipitation of the bone-like apatite. The dense precipitates exhibited a competitive Young's modulus value of approximately 120GPa, which was obtained through nanoindentation. This compared favorably to the calcium phosphate matrix. Differences in microstructure at various locations within the layer resulted in altered Young's modulus and microhardness values. Precipitation mechanism investigation was carried out through a comparative experiment. Chemical analysis showed that the precipitation of bone-like apatite on the calcium phosphate coating was quite conceivably a partial diffusion-controlled process. PMID:12485795

  10. Comment on "Apatite: A new redox proxy for silicic magmas?" [Geochimica et Cosmochimica Acta 132 (2014) 101-119

    NASA Astrophysics Data System (ADS)

    Marks, Michael A. W.; Scharrer, Manuel; Ladenburger, Sara; Markl, Gregor

    2016-06-01

    Recently Miles et al. (2014) proposed that a negative correlation between oxygen fugacity (expressed as logfO2 and the Mn content of apatite from a range of intermediate to silicic igneous rocks could be used as an oxybarometer (Eq. (1)).

  11. Characterization of mesostasis regions in lunar basalts: Understanding late-stage melt evolution and its influence on apatite formation

    NASA Astrophysics Data System (ADS)

    Potts, Nicola J.; TartèSe, Romain; Anand, Mahesh; Westrenen, Wim; Griffiths, Alexandra A.; Barrett, Thomas J.; Franchi, Ian A.

    2016-07-01

    Recent studies geared toward understanding the volatile abundances of the lunar interior have focused on the volatile-bearing accessory mineral apatite. Translating measurements of volatile abundances in lunar apatite into the volatile inventory of the silicate melts from which they crystallized, and ultimately of the mantle source regions of lunar magmas, however, has proved more difficult than initially thought. In this contribution, we report a detailed characterization of mesostasis regions in four Apollo mare basalts (10044, 12064, 15058, and 70035) in order to ascertain the compositions of the melts from which apatite crystallized. The texture, modal mineralogy, and reconstructed bulk composition of these mesostasis regions vary greatly within and between samples. There is no clear relationship between bulk-rock basaltic composition and that of bulk-mesostasis regions, indicating that bulk-rock composition may have little influence on mesostasis compositions. The development of individual melt pockets, combined with the occurrence of silicate liquid immiscibility, exerts greater control on the composition and texture of mesostasis regions. In general, the reconstructed late-stage lunar melts have roughly andesitic to dacitic compositions with low alkali contents, displaying much higher SiO2 abundances than the bulk compositions of their host magmatic rocks. Relevant partition coefficients for apatite-melt volatile partitioning under lunar conditions should, therefore, be derived from experiments conducted using intermediate compositions instead of compositions representing mare basalts.

  12. Characterization of mesostasis regions in lunar basalts: Understanding late-stage melt evolution and its influence on apatite formation

    NASA Astrophysics Data System (ADS)

    Potts, Nicola J.; TartèSe, Romain; Anand, Mahesh; Westrenen, Wim; Griffiths, Alexandra A.; Barrett, Thomas J.; Franchi, Ian A.

    2016-09-01

    Recent studies geared toward understanding the volatile abundances of the lunar interior have focused on the volatile-bearing accessory mineral apatite. Translating measurements of volatile abundances in lunar apatite into the volatile inventory of the silicate melts from which they crystallized, and ultimately of the mantle source regions of lunar magmas, however, has proved more difficult than initially thought. In this contribution, we report a detailed characterization of mesostasis regions in four Apollo mare basalts (10044, 12064, 15058, and 70035) in order to ascertain the compositions of the melts from which apatite crystallized. The texture, modal mineralogy, and reconstructed bulk composition of these mesostasis regions vary greatly within and between samples. There is no clear relationship between bulk-rock basaltic composition and that of bulk-mesostasis regions, indicating that bulk-rock composition may have little influence on mesostasis compositions. The development of individual melt pockets, combined with the occurrence of silicate liquid immiscibility, exerts greater control on the composition and texture of mesostasis regions. In general, the reconstructed late-stage lunar melts have roughly andesitic to dacitic compositions with low alkali contents, displaying much higher SiO2 abundances than the bulk compositions of their host magmatic rocks. Relevant partition coefficients for apatite-melt volatile partitioning under lunar conditions should, therefore, be derived from experiments conducted using intermediate compositions instead of compositions representing mare basalts.

  13. THE USE OF A TREATABILITY STUDY TO INVESTIGATE THE POTENTIAL FOR SELF HEATING & EXOTHERMIC REACTIONS IN DECONTAMINATION MATERIALS AT PFP

    SciTech Connect

    HOPKINS, A.M.

    2005-02-23

    Cerium Nitrate has been proposed for use in the decontamination of plutonium contaminated equipment at the Plutonium Finishing Plant (PFP) located on the Hanford Nuclear Reservation in eastern Washington. A Treatability Study was conducted to determine the validity of this decontamination technology in terms of meeting its performance goals and to understand the risks associated with the use of Cerium Nitrate under the conditions found at the PFP. Fluor Hanford is beginning the decommissioning of the PFP at the Hanford site. Aggressive chemicals are commonly used to remove transuranic contaminants from process equipment to allow disposal as low level waste. Chemicals being considered for decontamination of gloveboxes in PFP include cerium (IV) nitrate in a nitric acid solution, and proprietary commercial solutions that include acids, degreasers, and sequestering agents. Fluor's decontamination procedure involves application of the chemicals, followed by a wipe-down of the contaminated surfaces with rags. This process effectively transfers the decontamination liquids containing the transuranic materials to the rags, which can then be readily packaged for disposal as TRU waste. As part of a treatability study, Fluor Hanford and the Pacific Northwest National Laboratory (PNNL) have evaluated the potential for self-heating and exothermic reactions in the residual decontamination materials and the waste packages. Laboratory analyses and thermal-hydraulic modeling reveal a significant self-heating risk for cerium nitrate solutions when used with cotton rags. Exothermic reactions that release significant heat and off-gas have been discovered for cerium nitrate at higher temperatures. From these studies, limiting conditions have been defined to assure safe operations and waste packaging.

  14. 100-D Area In Situ Redox Treatability Test for Chromate-Contaminated Groundwater: FY 1998 Year-End Report

    SciTech Connect

    Williams, M.D.; Vermeul, V.R.; Szecsody, J.E.; Fruchter, J.S.; Cole, C.R.

    1999-04-15

    A treatability test was conducted for the In Situ Redox Manipulation (ISRM) technology at the US Department of Energy's Hanford, Washington 100D Area. The target contaminant was dissolved chromate [Cr(VI)] in groundwater. The ISRM technology involves creating a permeable subsurface treatment zone to reduce mobile chromate in groundwater to an insoluble form. The ISRM permeable treatment zone is created by reducing ferric iron [Fe(III)] to ferrous iron [Fe(II)] within the aquifer sediments. This is accomplished by injecting aqueous sodium dithionite into the aquifer and withdrawing the reaction products. The goal of the treatability test was to create a linear ISRM barrier by injecting sodium dithionite into five wells. Well installation and site characterization activities began in the spring of 1997. The first dithionite injection took place in September 1997. The results of this first injection were monitored through the spring of 1998; the remaining four dithionite injections were carried out in May through July of 1998. These five injections created a reduced zone in the Hanford unconfined aquifer 150 feet in length (perpendicular to groundwater flow) by 50 feet wide. The reduced zone extended over the thickness of the unconfined zone, which is approximately 15 feet. Analysis of recent groundwater sampling events shows that the concentrations of chromate [Cr(VI)] in groundwater in the reduced zone have been decreased from starting concentrations of approximately 900 ppb to below analytical detection limits (<7 ppb). Chromate concentrations are also declining in some downgradient monitoring wells. Laboratory analysis of iron in the soil indicates that the barrier should remain in place for approximately 20 to 25 years. These measurements will be confirmed by analysis of sediment cores in FY 1999.

  15. Apatite U-Pb thermochronolgy applied to complex geological settings - insights from geo/thermochronology and geochemistry

    NASA Astrophysics Data System (ADS)

    Paul, Andre; Spikings, Richard; Ulyanov, Alexey; Chew, David

    2016-04-01

    Application of high temperature (>350oC) thermochronology is limited to the U-Pb system of accessory minerals, such as apatite, under the assumption that radiogenic lead is lost to thermally activated volume diffusion into an infinite reservoir. Cochrane et al. (2015) have demonstrated a working example from the northern Andes of South America. Predictions from volume diffusion theory were compared with measured single grain U-Pb date correlated to shortest diffusion radius and in-situ profiles measured by LA-ICP-MS. Results from both techniques were found to be in agreement with predictions from thermally activated, volume diffusion. However, outliers from the ID-TIMS data suggested some complexity, as grains were found to be too young relative to their diffusion radius. Interaction of multiple processes can be responsible for the alteration of apatite U-Pb dates such as: (1) metamorphic (over)growth, (2) fluid aided alteration/recrystallization and (3) metamictization and fracturing of the grain. Further, predictions from volume diffusion rely on the input parameters: (a) diffusivity, (b) activation energy and (c) shortest diffusion radius. Diffusivity and activation energy are potentially influenced by the chemical composition and subsequent changes in crystal structure. Currently there is one value for diffusion parameter and activation energy established for (Durango) apatite (Cherniak et al., 1991). Correlation between diffusivity/activation energy and composition has not been established. We investigate if correlations exist between diffusivity/activation energy and composition by obtaining single grain apatite U-Pb date and chemical compostion and correlating these to their diffusion radius. We test the consistency of apatite closure temperature, by comparing the apatite U-Pb dates with lower temperature thermochronometers such as white mica and K-feldspar Ar/Ar and by petrographic observations. We test if chemical information can be a proxy to identify

  16. Determination of Sr and Ba partition coefficients between apatite from fish ( Sparus aurata) and seawater: The influence of temperature

    NASA Astrophysics Data System (ADS)

    Balter, Vincent; Lécuyer, Christophe

    2010-06-01

    The Sr/Ca and Ba/Ca ratios in inorganic apatite are strongly dependent on the temperature of the aqueous medium during precipitation. If valid in biogenic apatite, these thermometers would offer the advantage of being more resistant to diagenesis than those calibrated on biogenic calcite and aragonite. We have reared seabreams ( Sparus aurata) in tanks with controlled conditions during experiments lasting for more than 2 years at 13, 17, 23 and 27 °C, in order to determine the variations in Sr and Ba partitioning relative to Ca ( DSr and DBa, respectively) between seawater and fish apatitic hard tissues (i.e. teeth and bones), as a function of temperature. The sensitivity of the Sr and Ba thermometers (i.e. ∂ DSr/∂ T and ∂ DBa/∂ T, respectively), are similar in bone ( ∂Db-wSr/∂ T = 0.0036 ± 0.0003 and ∂Db-wBa/∂ T = 0.0134 ± 0.0026, respectively) and enamel ( ∂De-wSr/∂ T = 0.0037 ± 0.0005 and ∂De-wBa/∂ T = 0.0107 ± 0.0026, respectively). The positive values of ∂ DSr/∂ T and ∂ DBa/∂ T in bone and enamel indicate that DSr and DBa increase with increasing temperature, a pattern opposite to that observed for inorganic apatite. This distinct thermodependent trace element partitioning between inorganic and organic apatite and water highlights the contradictory effects of the crystal-chemical and biological controls on the partitioning of Ca, Sr and Ba in vertebrate organisms. Taking into account the diet Sr/Ca and Ba/Ca values, it is shown that the bone Ba/Ca signature of fish can be explained by Ca-biopurification and inorganic apatite precipitation, whereas both of these processes fail to predict the bone Sr/Ca values. Therefore, the metabolism of Ca as a function of temperature still needs to be fully understood. However, the biogenic Sr thermometer is used to calculate an average seawater temperature of 30.6 °C using the Sr/Ca compositions of fossil shark teeth at the Cretaceous/Tertiary boundary, and a typical seawater Sr

  17. Genesis of rare-metal pegmatites and alkaline apatite-fluorite rocks of Burpala massi, Northern Baikal folded zone

    NASA Astrophysics Data System (ADS)

    Sotnikova, Irina; Vladykin, Nikolai

    2015-04-01

    Burpalinsky rare metal alkaline massif in the Northern Baikal folded zone in southern margin of Siberian Platform, is a of intrusion central type, created 287 Ma covering area of about 250 km2. It is composed of nepheline syenites and pulaskites grading to quartz syenites in the contacts. Veines and dykes are represented by shonkinites, sodalite syenite, leucocratic granophyres, alkali granites and numerous rare metal alkaline syenite pegmatites and two dykes of carbonatites. All rocks except for granites are cut by a large apatite-fluorite dyke rocks with mica and magnetite, which in turn is cut by alaskite granites dyke. The massif has been studied by A.M. Portnov, A.A. Ganzeev et al. (1992) Burpalinsky massif is highly enriched with trace elements, which are concentrated in pegmatite dykes. About 70 rare-metal minerals we found in massif. Zr-silicates: zircon, eudialyte, lovenite, Ti-lovenite, velerite, burpalite, seidozerite, Ca- seidozerite, Rosenbuschite, vlasovite, katapleite, Ca-katapleite, elpidite. Ti- minerals:- sphene, astrophyllite, ramsaite, Mn-neptunite bafertisite, chevkinite, Mn-ilmenite, pirofanite, Sr-perrerit, landauite, rutile, anatase, brookite; TR- minerals - loparite, metaloparite, britolite, rinkolite, melanocerite, bastnesite, parisite, ankilite, monazite, fluocerite, TR-apatite; Nb- minerals - pyrochlore, loparite. Other rare minerals leucophanite, hambergite, pyrochlore, betafite, torite, thorianite, tayniolite, brewsterite, cryolite and others. We have proposed a new scheme massif: shonkinites - nepheline syenites - alkaline syenite - quartz syenites - veined rocks: mariupolites, rare-metal pegmatites, apatite, fluorite rock alyaskite and alkaline granites and carbonatites (Sotnikova, 2009). Apatite-fluorite rocks are found in the central part of massif. This is a large vein body of 2 km length and a 20 m width cutting prevailing pulaskites. Previously, these rocks were regarded as hydrothermal low-temperature phase. New geological and

  18. Fabrication and Intracellular Delivery of Doxorubicin/Carbonate Apatite Nanocomposites: Effect on Growth Retardation of Established Colon Tumor

    PubMed Central

    Chowdhury, Ezharul Hoque; Wu, Xin; Hirose, Hajime; Haque, Amranul; Doki, Yuichiro; Mori, Masaki; Akaike, Toshihiro

    2013-01-01

    In continuing search for effective treatments of cancer, the emerging model aims at efficient intracellular delivery of therapeutics into tumor cells in order to increase the drug concentration. However, the implementation of this strategy suffers from inefficient cellular uptake and drug resistance. Therefore, pH-sensitive nanosystems have recently been developed to target slightly acidic extracellular pH environment of solid tumors. The pH targeting approach is regarded as a more general strategy than conventional specific tumor cell surface targeting approaches, because the acidic tumor microclimate is most common in solid tumors. When nanosystems are combined with triggered release mechanisms in endosomal or lysosomal acidic pH along with endosomolytic capability, the nanocarriers demonstrated to overcome multidrug resistance of various tumors. Here, novel pH sensitive carbonate apatite has been fabricated to efficiently deliver anticancer drug Doxorubicin (DOX) to cancer cells, by virtue of its pH sensitivity being quite unstable under an acidic condition in endosomes and the desirable size of the resulting apatite-DOX for efficient cellular uptake as revealed by scanning electron microscopy. Florescence microscopy and flow cytometry analyses demonstrated significant uptake of drug (92%) when complexed with apatite nanoparticles. In vitro chemosensitivity assay revealed that apatite-DOX nanoparticles executed high cytotoxicity in several human cancer cell lines compared to free drugs and consequently apatite-DOX-facilitated enhanced tumor inhibitory effect was observed in colorectal tumor model within BALB/cA nude mice, thereby shedding light on their potential applications in cancer therapy. PMID:23613726

  19. Crystallinity and compositional changes in carbonated apatites: Evidence from {sup 31}P solid-state NMR, Raman, and AFM analysis

    SciTech Connect

    McElderry, John-David P.; Zhu, Peizhi; Mroue, Kamal H.; Xu, Jiadi; Pavan, Barbara; Fang, Ming; Zhao, Guisheng; McNerny, Erin; Kohn, David H.; Franceschi, Renny T.; Holl, Mark M.Banaszak; Tecklenburg, Mary M.J.; Ramamoorthy, Ayyalusamy; Morris, Michael D.

    2013-10-15

    Solid-state (magic-angle spinning) NMR spectroscopy is a useful tool for obtaining structural information on bone organic and mineral components and synthetic model minerals at the atomic-level. Raman and {sup 31}P NMR spectral parameters were investigated in a series of synthetic B-type carbonated apatites (CAps). Inverse {sup 31}P NMR linewidth and inverse Raman PO{sub 4}{sup 3−}ν{sub 1} bandwidth were both correlated with powder XRD c-axis crystallinity over the 0.3–10.3 wt% CO{sub 3}{sup 2−} range investigated. Comparison with bone powder crystallinities showed agreement with values predicted by NMR and Raman calibration curves. Carbonate content was divided into two domains by the {sup 31}P NMR chemical shift frequency and the Raman phosphate ν{sub 1} band position. These parameters remain stable except for an abrupt transition at 6.5 wt% carbonate, a composition which corresponds to an average of one carbonate per unit cell. This near-binary distribution of spectroscopic properties was also found in AFM-measured particle sizes and Ca/P molar ratios by elemental analysis. We propose that this transition differentiates between two charge-balancing ion-loss mechanisms as measured by Ca/P ratios. These results define a criterion for spectroscopic characterization of B-type carbonate substitution in apatitic minerals. - Graphical abstract: Carbonated apatite shows an abrupt change in spectral (NMR, Raman) and morphological (AFM) properties at a composition of about one carbonate substitution per unit cell. Display Omitted - Highlights: • Crystallinity (XRD), particle size (AFM) of carbonated apatites and bone mineral. • Linear relationships among crystallinity, {sup 31}P NMR and Raman inverse bandwidths. • Low and high carbonated apatites use different charge-balancing ion-loss mechanism.

  20. A re-evaluation of geological timescale benchmarks and temperature sensitivity of fission-track annealing in apatites

    NASA Astrophysics Data System (ADS)

    Luijendijk, Elco; Andriessen, Paul

    2016-04-01

    Current models of the temperature sensitivity of fission track annealing in apatites have been calibrated using fission track data from boreholes, with the assumption that these samples are currently at maximum burial depth and temperatures. The most detailed data-set comes from boreholes located in the Otway basin, Australia. However, several lines of evidence suggest that these samples are not at their maximum burial depth and temperature and consequently the cooling temperature of the apatite fission track thermochronometer would then be higher than previously assumed. Significant late Cenozoic exhumation in the Otway Basin was suggested by earlier studies that document a major late-Miocene erosional unconformity, folding and trusting of underlying sediments and elevated strandlines along the coast. In addition, anomalously young apatite (U-Th)/He ages in several boreholes in the basin suggest that the basin's sediments have been exhumed and cooled in the late Cenozoic. We explore the effects of late Cenozoic exhumation on fission track data in the Otway basin using a 1D model of burial and thermal history. We show that simulating several 100s of meters of exhumation in the basin results in significant misfit between current annealing models and observed fission track data. The additional exhumation reconciles the Otway basin data with a second detailed fission track dataset from boreholes in Southern Texas with a well-constrained thermal and burial history. We combine vitrinite reflectance data and U-Th/He data from the Otway basin to recalibrate the burial history of the Otway basin. Subsequently we combine the new thermal history of the Otway basin with the Southern Texas dataset to recalibrate the fission track annealing algorithm. The results suggest that fission-track annealing in apatites is underestimated by approximately 20°C by current annealing models, with significant implications for studies that use apatite fission track thermochronology to

  1. The influence of burial heating on the (U-Th)/He system in apatite: Grand Canyon case study

    NASA Astrophysics Data System (ADS)

    Fox, Matthew; Shuster, David L.

    2014-07-01

    Thermochronological data can constrain the cooling paths of rocks exhumed through the uppermost 1-2 km of earth's crust, and have thus been pivotal in illuminating topographic development over timescales >0.1 Ma. However, in some cases, different methods have led to conflicting conclusions about timing of valley-scale exhumation. Here, we investigate the case of Western Grand Canyon, USA, where different thermochronological datasets have been interpreted to record very different timings of canyon incision (∼70 Ma versus ∼5 Ma). We present a method to assess key assumptions in these constraints and demonstrate that burial heating conditions of basement rocks in the Mesozoic can result in incomplete annealing of radiation damage in apatite. In turn, this has a dramatic effect on the temperature sensitivity of the apatite (U-Th)/He system and its ability to record post-burial exhumation. The possibility of incomplete annealing resolves the apparent conflict in time-temperature paths inferred over the last 70 Ma, although it requires temperatures during burial that are lower than predicted by apatite fission track data. A refinement of parameters that prescribe the kinetics of damage annealing and related control on 4He diffusivity in apatite would account for this discrepancy, specifically if alpha recoil damage anneals at a lower rate than fission tracks at a given temperature. These effects will be important for any application of the apatite (U-Th)/He system in geologic settings that experienced prolonged residence (>10 Ma) between 50-150 °C; the approaches developed here provide means to assess these effects.

  2. Microstructure and electrical conductivity of apatite-type La10Si6-xWxO27+δ electrolytes

    NASA Astrophysics Data System (ADS)

    Xiang, Jun; Ouyang, Jia-Hu; Liu, Zhan-Guo

    2015-06-01

    Different compositions of apatite-type La10Si6-xWxO27+δ ceramics are prepared successfully by the high-temperature solid state reaction route. Crystal structure and electrical properties of La10Si6-xWxO27+δ ceramics are investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM) with energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM) and electrochemical impedance spectroscopy (EIS). La10Si6-xWxO27+δ (x = 0.1, 0.2, 0.3, 0.4, 0.5) ceramics consist of a hexagonal apatite-type structure and a small amount of La6W2O15 phase of orthorhombic structure but no La2SiO5 phase. The diffraction peaks of the hexagonal apatite-type structure shift to the low angle side with doping the W6+. When the content of hexavalent tungsten is beyond 0.1, rod-like grains of La10Si6-xWxO27+δ ceramics are replaced gradually by equiaxed apatite-type grains, and some fine particles of La6W2O15 are observed at grain boundaries. These La6W2O15 particles are non-conducting materials and lead to the increase in grain impedance and grain boundary impedance of La10Si6-xWxO27+δ ceramics gradually when the content of hexavalent tungsten is beyond 0.2. However, the solid solubility of W6+ in the lattice of apatite-type structure reaches the maximum when the W6+ content is at 0.1, and correspondingly the La10Si5.9W0.1O27.1 ceramic has the highest total conductivity of 4.45 × 10-2 S cm-1 at 1073 K.

  3. Structural and phase transformation of apatite and quartz in the indentation process single crystals

    SciTech Connect

    Chaikina, Marina

    2014-11-14

    Using the method of scanning and high-resolution electron microscopy, the zones of indentation by scratching for apatite and quartz single crystals were investigated. The textural, structural and phase transformations revealed have been conventionally ascribed to “deformation” and “diffusion” processes of plastic deformation. In zones of indentation by scratching of single crystals there have been two levels of structural transformations revealed, with a sharp boundary between them, at a stress equal to the theoretical ultimate stress limit (σ{sub TSL}). In the top zone of scratches, within the range of stress from the microhardness value H{sub s} up to the σ{sub TSL} value the substance undergoes profound structural and phase transformations. In the bed of scratches at the stress value lower than σ{sub TSL} values, single crystal fragmentation occurs with the formation of blocks and steps.

  4. Chemical solution deposition of the highly c-axis oriented apatite type lanthanum silicate thin films.

    PubMed

    Hori, Shigeo; Takatani, Yasuhiro; Kadoura, Hiroaki; Uyama, Takeshi; Fujita, Satoru; Tani, Toshihiko

    2015-10-28

    Highly c-axis oriented apatite-type lanthanum silicate (LSO) thin films were fabricated by a simple solution coating method. In the solution coating method, LSO thin films are obtained by crystallization of initially deposited amorphous LSO precursor thin films. The degree of orientation was influenced by the precursor morphologies and a dense LSO precursor led to a high c-axis orientation perpendicular to the substrate. The oriented LSO thin films were composed of columnar grains with a single crystal orientation over the entire film thickness. In-plane orientation was not detected, which indicates that the c-axis orientation of the LSO thin films can be attributed to self-orientation. PMID:26391101

  5. Experimental osteoinduction in rats: collagen-apatite versus osteogenin-containing gelatine.

    PubMed

    Schwarz, N; Redl, H; Schlag, G; Lintner, F; Dinges, H P; Thurnher, M; Schiesser, A

    1987-01-01

    An experimental study in rats was done to investigate the bone-regenerating properties of collagen apatite (Collapat) and to compare it with osteoinduction dependent on osteogenin-containing gelatine (OCG). The test substances were implanted orthotopically (calvarial defect--7 mm in diameter) and heterotopically (paravertebral muscles, abdominal muscles). The results were evaluated histologically and enzymatically (alkaline phosphatase). Collapat caused neither osteoinduction in the heterotopic site nor healing of the bone defects. Foreign body reaction without new bone formation was encountered. OCG implantation leads to new bone formation in the muscles within 3 weeks, associated with a significant increase in alkaline phosphatase activity, and to extensive new bone formation in the calvarial defect within 4 weeks. The defects did not heal if left empty. The value of clinical application of Collapat appears to be doubtful. Osteoinduction with OCG requires further experimental investigation. PMID:3551878

  6. Fish Canyon Tuff Apatite: A New Look At An Old Low-Temperature Thermochronology Standard

    NASA Astrophysics Data System (ADS)

    Kohn, B. P.; Gleadow, A. J.; Harrison, M.; Lugo-Zazueta, R.

    2011-12-01

    Fish Canyon Tuff (FCT) is one of the most voluminous (>5,000 km3) ignimbrite eruptions documented on Earth. It erupted over a relatively short period from the ~80 km x 30 km La Garita caldera, San Juan volcanic field, Colorado and has served as an important source for geochronology standards, particularly for K-Ar, 40Ar/39Ar and fission track dating [e.g. 1-6]. Ar and U/Pb studies over many years to determine the age of FCT have resulted in disagreement [e.g. 3-5] and this has compromised the potential use of some FCT minerals as geochronology standards. However, a recent study, reporting an improved assessment of the 40K decay constants indicates a 40Ar/39Ar sanidine age of 28.305±0.036 Ma, which can also be reconciled with U/Pb zircon data [6]. In an effort to evaluate the suitability of FCT apatite as a standard for (U-Th-Sm)/He (AHe) thermochronometry we analysed samples from the lithic-rich classic site, some 8.7 km SW of South Fork, Colorado used for early fission track and Ar studies [1-2] and also from a ~330 m vertical section of FCT above that site. Average weighted mean AHe ages (±95% confidence level) from multiple analyses at five sites range from 20.5±1.5 Ma to 23.3±2.2 Ma. Apatite fission track (AFT) ages from the same samples determined by automated image capture and counting, in combination with LA-ICP-MS for U determination, range from 28.4±1.2 Ma at the classic site to 23.3±1.6 Ma at the top of the measured profile. AFT ages can be related to kinetic parameters Dpar and Cl content which are highest (2.19±0.3 μm and 0.73-0.87 wt % respectively) at the classic site, but vary through the profile. AHe and some AFT data provide strong evidence for substantial post-eruptive Early Miocene cooling of the FCT from temperatures estimated between >~80°C to ~110°C, and attributed to km-scale erosion, possibly triggered by structural changes related to formation of the nearby Rio Grande rift. Despite evidence for some later cooling, FCT apatite at

  7. Ion microprobe U-Pb dating and REE abundance of biogenic apatite

    NASA Astrophysics Data System (ADS)

    Sano, Y.; Terada, K.; Ueki, S.

    2001-12-01

    If the direct U-Pb dating of a fossil itself is possible, the method could have great impact on stratigraphic studies in establishing the absolute chronology of sedimentary sequences. Micro fossil ?conodont? are candidates for this purpose since they consist of apatite (Ca2(PO5)3 (F,Cl,OH)), which would uptake U, Th and Pb after sedimentation no longer than a few million years and is supposed to remain closed to U and Pb under relatively low effective closure temperature. We report here results of direct ion microprobe U-Th-Pb dating of two conodonts; Trichognathus from Kinderhookian stage of Mississippian sedimentary sequence from Illinois Basin region in North America and Panderodus from a Llandoverian sedimentary sequence on Langkawi Island, northern Malaysia. Secondary purpose of the study is to indicate in situ analysis of all REE on the same spots of U-Pb measurements. Samples were cast into epoxy resin discs with a few grains of standard apatite, PRAP, derived from an alkaline rock of Prairie Lake circular complex in the Canadian Shield and polished until they were exposed through their mid-sections. U, Th and REE abundances, and Pb isotopic compositions were measured by using SHRIMP installed at Hiroshima University. Thirteen spots on Trichognathus yield a 238U/206Pb isochron age of 323+/-36 Ma, which is consistent with the depositional and early diagenetic ages. Fifteen spots on Panderodus give 232Th/208Pb isochron age of 429+/-50 Ma, which is again comparable to an early Silurian. Shale-normalized REE of Trichognathus shows a broadly flat pattern from light to middle REE and a decrease from middle to heavy REE with negative anomalies of Ce and Eu. In contrast Panderodus indicates a concave-shape pattern with middle REE enrichment. These characteristics are probably due to a different formation environment as suggested by other workers.

  8. Phase transition and mixed oxide-proton conductivity in germanium oxy-apatites

    SciTech Connect

    Leon-Reina, Laura; Porras-Vazquez, Jose M.; Losilla, Enrique R.; Aranda, Miguel A.G.

    2007-04-15

    La{sub 9.75}{open_square}{sub 0.25}(Ge{sub 6}O{sub 24})O{sub 2.62} oxy-apatite shows a phase transition from triclinic to hexagonal symmetry at approximately 1020 K that has been characterised by high-temperature synchrotron X-ray and neutron powder diffraction, and ionic conductivity measurements. The crystal structure at 1073 K has been determined from joint Rietveld refinements of synchrotron X-ray and neutron powder diffraction data. The study shows that hexagonal-La{sub 9.75}{open_square}{sub 0.25}(Ge{sub 6}O{sub 24})O{sub 2.62} contains interstitial oxygen at the position previously reported for other oxy-germanates. Changes in the oxide conductivity associated with this structural transition are discussed. The thermal analyses showed a weight loss on heating close to 600 K very likely due to water release. The synchrotron thermodiffractometric study shows an anomaly in the cell parameters evolution at that temperature, which indicates that this residual water is located into the apatite channels. The electrical characterisation under different atmospheres (dry and wet synthetic air) indicates that there is a significant proton contribution to the overall conductivity below 600 K, mainly under wet atmosphere. - Graphical abstract: La{sub 9.75}{open_square}{sub 0.25}(Ge{sub 6}O{sub 24})O{sub 2.62} oxide-conductor shows triclinic-hexagonal phase transition (see inset) at {approx}1020 K, meanwhile La{sub 9.55}{open_square}{sub 0.45}(Ge{sub 6}O{sub 24})O{sub 2.32} is hexagonal at all temperatures. Both compounds have mixed proton and oxide conductivities below 600 K.

  9. Nanomedicine: Interaction of biomimetic apatite colloidal nanoparticles with human blood components.

    PubMed

    Choimet, Maëla; Hyoung-Mi, Kim; Jae-Min, Oh; Tourrette, Audrey; Drouet, Christophe

    2016-09-01

    This contribution investigates the interaction of two types of biomimetic-apatite colloidal nanoparticles (negatively-charged 47nm, and positively-charged 190nm NPs) with blood components, namely red blood cells (RBC) and plasma proteins, with the view to inspect their hemocompatibility. The NPs, preliminarily characterized by XRD, FTIR and DLS, showed low hemolysis ratio (typically lower than 5%) illustrating the high compatibility of such NPs with respect to RBC, even at high concentration (up to 10mg/ml). The presence of glucose as water-soluble matrix for freeze-dried and re-dispersed colloids led to slightly increased hemolysis as compared to glucose-free formulations. NPs/plasma protein interaction was then followed, via non-specific protein fluorescence quenching assays, by contact with whole human blood plasma. The amount of plasma proteins in interaction with the NPs was evaluated experimentally, and the data were fitted with the Hill plot and Stern-Volmer models. In all cases, binding constants of the order of 10(1)-10(2) were found. These values, significantly lower than those reported for other types of nanoparticles or molecular interactions, illustrate the fairly inert character of these colloidal NPs with respect to plasma proteins, which is desirable for circulating injectable suspensions. Results were discussed in relation with particle surface charge and mean particle hydrodynamic diameter (HD). On the basis of these hemocompatibility data, this study significantly complements previous results relative to the development and nontoxicity of biomimetic-apatite-based colloids stabilized by non-drug biocompatible organic molecules, intended for use in nanomedicine. PMID:27137807

  10. A Sequential Leach Method and Pb Isotope Approach to Studying Apatite Weathering in Granitoid Soils at Hubbard Brook Experimental Forest, NH, USA

    NASA Astrophysics Data System (ADS)

    Nezat, C. A.; Blum, J. D.

    2005-12-01

    Easily dissolved minerals such as calcite and apatite can be important in controlling stream and ground water chemistry even though these minerals are only present in trace amounts in granitoid rocks. Because of its solubility, apatite, a calcium phosphate mineral, may be a significant source of essential nutrients (especially phosphorous) for vegetation, and has been shown to strongly influence stream and soil water composition (e.g, calcium, strontium and rare earth elements). There are additional sources of Ca (e.g., feldspars, hornblende) and P (e.g., organic matter or bound to Fe and Al oxides) in granitoid soils. In order to distinguish the chemical constituents of apatite from other pools in the bulk soil, we selectively dissolved apatite with a dilute acid leach, and measured Pb isotopic ratios of apatite, feldspar, and leachates. We tested the leaching procedure on mineral separates and verified that a dilute nitric solution primarily dissolves apatite. Silicates were dissolved in subsequent steps by successively stronger acids. We then applied this method to bulk soils collected from several soil pits across a small watershed at the Hubbard Brook Experimental Forest (HBEF), New Hampshire, USA, to determine the spatial distribution of Ca and P pools, and determine the depth of apatite depletion in the soil. We also measured Pb isotope ratios in the soil leachates to distinguish among the various sources of Pb (e.g., apatite, feldspars and anthropogenic sources). We found that Pb in the dilute nitric leach of the HBEF organic soils is dominated by anthropogenic sources and that Pb from apatite becomes increasingly important with depth.

  11. Synthesis of trace element bearing single crystals of Chlor-Apatite (Ca5(PO4)3Cl) using the flux growth method

    PubMed Central

    2013-01-01

    We present a new strategy on how to synthesize trace-element bearing (REE, Sr) chlorapatites Ca5(PO4)3Cl using the flux growth method. Synthetic apatites were up to several mm long, light blue in colour. The apatites were characterized using XRD, electron microprobe and laser ablation ICP-MS (LA-ICPMS) techniques and contained several hundred μg/g La, Ce, Pr, Sm, Gd and Lu and about 1700 μg/g Sr. The analyses indicate that apatites were homogenous (within the uncertainties) for major and trace elements. PMID:23531340

  12. Synthesis of trace element bearing single crystals of Chlor-Apatite (Ca5(PO4)3Cl) using the flux growth method.

    PubMed

    Klemme, Stephan; John, Timm; Wessels, Mathias; Kusebauch, Christof; Berndt, Jasper; Rohrbach, Arno; Schmid-Beurmann, Peter

    2013-01-01

    We present a new strategy on how to synthesize trace-element bearing (REE, Sr) chlorapatites Ca5(PO4)3Cl using the flux growth method. Synthetic apatites were up to several mm long, light blue in colour. The apatites were characterized using XRD, electron microprobe and laser ablation ICP-MS (LA-ICPMS) techniques and contained several hundred μg/g La, Ce, Pr, Sm, Gd and Lu and about 1700 μg/g Sr. The analyses indicate that apatites were homogenous (within the uncertainties) for major and trace elements. PMID:23531340

  13. Partitioning behavior of chlorine and fluorine in the system apatite melt fluid. II: Felsic silicate systems at 200 MPa

    NASA Astrophysics Data System (ADS)

    Webster, James D.; Tappen, Christine M.; Mandeville, Charles W.

    2009-02-01

    Hydrothermal experiments were conducted to determine the partitioning of Cl between rhyolitic to rhyodacitic melts, apatite, and aqueous fluid(s) and the partitioning of F between apatite and these melts at ca. 200 MPa and 900-924 °C. The number of fluid phases in our experiments is unknown; they may have involved a single fluid or vapor plus saline liquid. The partitioning behavior of Cl between apatite and melt is non-Nernstian and is a complex function of melt composition and the Cl concentration of the system. Values of DClapat/melt (wt. fraction of: Cl in apatite/Cl in melt) vary from 1 to 4.5 and are largest when the Cl concentrations of the melt are at or near the Cl-saturation value of the melt. The Cl-saturation concentrations of silicate melts are lowest in evolved, silica-rich melts, so with elevated Cl concentrations in a system and with all else equal, the maximum values of DClapat/melt occur with the most felsic melt. In contrast, values of DFapat/melt range from 11 to 40 for these felsic melts, and many of these are an order of magnitude greater than those applying to basaltic melts at 200 MPa and 1066-1150 °C. The Cl concentration of apatite is a simple and linear function of the concentration of Cl in fluid. Values of DClfluid/apat for these experiments range from 9 to 43, and some values are an order of magnitude greater than those determined in 200-MPa experiments involving basaltic melts at 1066-1150 °C. In order to determine the concentrations and interpret the behavior of volatile components in magmas, the experimental data have been applied to the halogen concentrations of apatite grains from chemically evolved rocks of Augustine volcano, Alaska; Krakatau volcano, Indonesia; Mt. Pinatubo, Philippines; Mt. St. Helens, Washington; Mt. Mazama, Oregon; Lascar volcano, Chile; Santorini volcano, Greece, and the Bishop Tuff, California. The F concentrations of these magmas estimated from apatite-melt equilibria range from 0.06 to 0.12 wt% and are

  14. Treatability Study Operational Testing Program and Implementation Plan for the Gunite and Associated Tanks at the Oak Ridge National Laboratory, Oak Ridge, Tennessee

    SciTech Connect

    1996-09-01

    To support future decision making of the Gunite and Associated Tanks (GAAT) Operable Unit (OU) remedy selection, the Department of Energy (DOE) is performing a Treatability Study (TS), consistent with the EPA guidance for Comprehensive Environmental Response, compensation, and Liability Act (CERCLA) treatability studies. The study will inform stakeholders about various waste removal technologies and the cost of potential remediation approaches, particularly the cost associated with sluicing and the reduction in risk to human health and the environment from tank content removal. As part of the GAAT OU remedy, a series of studies and technology tests will be preformed. These may address one or more of the following areas, characterization, removal, treatment, and transfer of wastes stored in the GAAT OU.

  15. Reply to comment by Marks et al. (2016) on "Apatite: A new redox proxy for silicic magmas?" [Geochimica et Cosmochimica Acta 132 (2014) 101-119

    NASA Astrophysics Data System (ADS)

    Miles, Andrew; Graham, Colin; Hawkesworth, Chris; Gillespie, Martin; Hinton, Richard; Bromiley, Geoffrey

    2016-06-01

    Marks et al. (2016) investigate the applicability of the Mn-in-apatite oxybarometer proposed by Miles et al. (2014) across a range of magma compositions using published data on well-characterised samples. The authors show that for magma compositions outside of the calc-alkaline and intermediate to silicic range used in the preliminary calibration, fO2 values calculated from Mn-in-apatite vary significantly from independently constrained estimates. These data are used to reiterate our warnings that other controls that are additional to oxygen fugacity are likely to affect Mn partitioning into apatite in some rock types, and particularly so in magmas that lie outside of the range of compositions and conditions used in the calibration. Marks et al. (2016) highlight that temperature may have an especially important effect on Mn partitioning in apatite in some rock types.

  16. Waste management plan for phase II of the Bear Creek Valley Treatability study Oak Ridge Y-12 Plant, Oak Ridge, Tennessee

    SciTech Connect

    1997-09-01

    This Waste Management Plan (WMP) for the Bear Creek Valley Treatability Study addresses waste management requirements for the Oak Ridge Y-12 Plant. The study is intended to produce treatment performance data required to design a treatment system for contaminated groundwater. The treatability study will consist of an evaluation of various treatment media including continuous column tests, with up to six columns being employed to evaluate the performance of different media in the treatment of groundwater; an evaluation of the dentrifying capacity and metal uptake capacity of a wetland system; and the long-term dentrifying capacity and metal uptake capacity of algal mats. Additionally, the treatability study involves installation of a trench and incline well to evaluate and assess hydraulic impacts of pumping groundwater. The Sampling and Analysis Plan (SAP) covers the project description, technical objectives, procedures, and planned work activities in greater detail. The Health and Safety Plan (HASP) addresses the health and safety concerns and requirements for the proposed sampling activities. This WMP identifies the types and estimates the volumes of various wastes that may be generated during the proposed treatability studies. The approach to managing waste outlined in this WMP emphasizes the following points: (1) management of the waste generated in a manner that is protective of human health and the environment; (2) minimization of waste generation, thereby reducing unnecessary costs and usage of limited permitted storage and disposal capacities; and (3) compliance with federal, state, and site requirements. Prior sampling at the site has detected organic, radioactive, and metals contamination in groundwater and surface water. Proposed field operations are not expected to result in worker exposures greater than applicable exposure or action limits.

  17. United States Air Force 611th Civil Engineer Squadron, Elmendorf AFB, Alaska installation restoration program, remedial investigation/feasibility study, Galena Airport, Alaska. Treatability study report. Final report

    SciTech Connect

    1995-01-27

    The USAF contracted Radian Corporation to perform treatability studies to evaluate soil vacuum extraction (SVE) and biodegradation technologies for remediating soil contaminated with motor and jet fuel at the Petroleum, Oils, and Lubricants (POL) Tank Farm, Galena Airport, Alaska. This technical report describes the experimental methods and interprets the analytical and operational results from the bench-scale biotreatment tests and pilot-scale SVE tests conducted between July 1992 and February 1994.

  18. Evidence for the exsolution of Cl-rich fluids in martian magmas: Apatite petrogenesis in the enriched lherzolitic shergottite Northwest Africa 7755

    NASA Astrophysics Data System (ADS)

    Howarth, G. H.; Pernet-Fisher, J. F.; Bodnar, R. J.; Taylor, L. A.

    2015-10-01

    Martian meteorite Northwest Africa 7755 is a new example of an enriched, lherzolitic shergottite, containing some of the coarsest-grained apatite yet identified in shergottite meteorites. Their size has permitted detailed observations of volatile distributions within single grains. We have demonstrated that some apatites have been invaded by shock melts, which act to devolatilize parts of grains, resulting in significant Cl-enrichment in the adjacent regions. The extent of chemical heterogeneity within single grains must be carefully considered in other shergottites, so that the effects of secondary modification of apatites are well-constrained, prior to interpreting the volatile contents and primary magmatic processes. Apatite grains unaffected by shock melts are OH-F enriched and Cl-poor (∼F50Cl14OH36), relative to interstitial apatites reported in other shergottites. The volatile compositions are similar to interstitial apatites reported in terrestrial mafic intrusions. Such apatites in terrestrial intrusions are argued to have formed after significant Cl-loss due to the exsolution and migration of Cl-rich brines. Calculated relative F2, Cl2, and H2O fugacities for NWA 7755 apatites show a trend of degassing rather than fractionation, noted in previous studies. Indeed, we interpret the volatile contents of apatites analyzed in the cumulate shergottite NWA 7755 to represent snapshots of the evolving late-stage residual liquid during exsolution of a Cl-rich brine. This fluid phase has subsequently been lost from an open magma system, migrating upward through the cumulate sequence enriching residual liquids in Cl. Alternatively, it formed a hydrothermal system in the martian crust surrounding the intrusion. Furthermore, by comparison with terrestrial examples, we suggest that the late-stage evolution of volatile-bearing phases in NWA 7755 is similar to that of comparable terrestrial mafic rocks. Primary cumulus apatites are F-rich, whereas interstitial apatites

  19. Lu-Hf isotope systematics of fossil biogenic apatite and their effects on geochronology

    NASA Astrophysics Data System (ADS)

    Herwartz, Daniel; Münker, Carsten; Tütken, Thomas; Hoffmann, J. Elis; Wittke, Andreas; Barbier, Bruno

    2013-01-01

    Reliable methods for direct dating of biogenic apatite from pre-Pleistocene fossils are currently not available, and recent attempts using the Lu-Hf decay system yielded highly inaccurate ages for both bones and teeth. The geological processes accounting for this poor accuracy of Lu-Hf chronometry are not yet understood. Here we explore Lu-Hf systematics in fossil bones and teeth in detail, by applying five different sample digestion techniques that are tested on bones and composites of bone and sediment. Our current dataset implies that dissolution methods only slightly affect the resulting Lu-Hf ages, while clear differences between the individual digestion techniques became apparent for element concentrations. By analysing the insoluble leftovers from incomplete sample dissolution, four main reservoirs of Hf in fossil bones were identified: (1) a radiogenic end-member associated with apatite; (2) an unradiogenic end-member represented by the authigenic minerals or the embedding sediment; (3) a highly unradiogenic end-member that can be attributed to detrital zircon; and (4) a moderately soluble phase (probably a Zr(Hf)-phosphate) that yielded very low Lu/Hf but a highly radiogenic Hf isotope composition at the same time. This Zr(Hf)-phase must have been precipitated within the fossil bone sample at a late stage of burial history, thereby incorporating radiogenic 176Hf released from apatite surfaces over geological timescales. A second focus of our study is the effect of different sediment matrices and of crystal size on the preservation of pristine Lu-Hf isotope compositions in bioapatite. Because near-depositional Lu-Hf ages of phosphate fossils have previously been reported for the London Clay (England) and a calcareous marl from Tendaguru (Tanzania), we herein investigate specimens fossilised in carbonate matrices (calcareous marl from Oker, Germany; carbonate concretions from the Santana Formation, Brazil; carbonate from the Eifel, Germany) and argillaceous

  20. Safety analysis report for the North Tank Farm, Tank W-11, and the Gunite and Associated Tanks -- Treatability Study, Oak Ridge National Laboratory, Oak Ridge, Tennessee

    SciTech Connect

    Platfoot, J.H.

    1997-02-01

    The North Tank Farm (NTF) tanks consist of eight underground storage tanks which have been removed from service because of age and changes in liquid waste system needs and requirements. Tank W-11, which was constructed in 1943, has been removed from service, and contains several hundred gallons of liquid low-level waste (LLLW). The Gunite and Associated Tanks (GAAT) Treatability Study involves the demonstration of sludge removal techniques and equipment for use in other waste storage tanks throughout the Department of Energy (DOE) complex. The hazards associated with the NTF, Tank W-11, and the Treatability Study are identified in hazard identification table in Appendixes A, B, and C. The hazards identified for the NTF, Tank W-11, and the Treatability Study were analyzed in the preliminary hazards analyses (PHA) included as Appendices D and E. The PHA identifies potential accident scenarios and qualitatively estimates the consequences. Because of the limited quantities of materials present in the tanks and the types of energy sources that may result in release of the materials, none of the accidents identified are anticipated to result in significant adverse health effects to on-site or off-site personnel.

  1. Apatite/Melt Partitioning Experiments Reveal Redox Sensitivity to Cr, V, Mn, Ni, Eu, W, Th, and U

    NASA Technical Reports Server (NTRS)

    Righter, K.; Yang, S.; Humayun, M.

    2016-01-01

    Apatite is a common mineral in terrestrial, planetary, and asteroidal materials. It is commonly used for geochronology (U-Pb), sensing volatiles (H, F, Cl, S), and can concentrate rare earth elements (REE) during magmatic fractionation and in general. Some recent studies have shown that some kinds of phosphate may fractionate Hf and W and that Mn may be redox sensitive. Experimental studies have focused on REE and other lithophile elements and at simplified or not specified oxygen fugacities. There is a dearth of partitioning data for chalcophile, siderophile and other elements between apatite and melt. Here we carry out several experiments at variable fO2 to study the partitioning of a broad range of trace elements. We compare to existing data and then focus on several elements that exhibit redox dependent partitioning behavior.

  2. In-situ Strontium Isotopes Analysis on Single Conodont Apatite by LA-MC-ICP-MS

    NASA Astrophysics Data System (ADS)

    Zhao, L.; Zhang, L.; Chen, Z. Q.; Ma, D.; Qiu, H.; Lv, Z.; Hu, Z.; Wang, F.

    2014-12-01

    Strontium isotope played an important role in stratigraphic chronology and sedimentary geochemistry research (McArthur et al., 2001). Conodonts is a kind of extinct species of marine animals and widely distributed in marine sediments all over the world. Rich in radiogenic Sr contents and difficulty to be affected during diagenesis alteration makes conodonts a good choice in seawater Sr isotope composition studies (John et al., 2008). Conodont samples were collected from 24th to 39th layer across Permian-Triassic boundary at Meishan D section (GSSP), Zhejiang Province, South China (Yin et al., 2001). Conodonts was originated from fresh limestone and only conodont elements with CAI<2 were chosen for in-situ strontium isotope analysis using laser-ablation multi-collector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS). Conodont samples are from totally 25 layers in seven conodont zones making it possible for a high resolution 87Sr/ 86Sr curve reconstruction during the Permian-Triassic transition. 87Sr/ 86Sr ratio kept a relatively high value (0.70752) in the middle part of the Clarkina yini zone and a lower value (0.70634) in the upperpart of Clarkina taylorae zone. Of which, 87Sr/ 86Sr ratio emerged a rapid decrease within the Clarkina taylorae zone. After a subsequent increase, 87Sr/ 86Sr ratio dropped to 0.70777 in the Isarcicella staeschei zone. These results helps providing reference data for the biological mass extinction events during the Permian-Triassic transition. Our study also makes is possible for high resolution 87Sr/ 86Sr ratio testing on the single conodont apatite and riched the in-situ studies on the conodont apatite, which of great significance for the future conodont Sr isotope research (Zhao et al., 2009; Zhao et al., 2013). Keywords: Conodonts, Strontium isotope, LA-MC-ICP-MS, Permian-Triassic transition, Meishan D section [1] John et al., 2008 3P[2] McArthur et al., 2001 J. of Geology [3] Yin et al., 2001 Episodes [4] Zhao et al

  3. Authigenic apatite and octacalcium phosphate formation due to adsorption-precipitation switching across estuarine salinity gradients

    NASA Astrophysics Data System (ADS)

    Oxmann, J. F.; Schwendenmann, L.

    2015-02-01

    Mechanisms governing phosphorus (P) speciation in coastal sediments remain largely unknown due to the diversity of coastal environments and poor analytical specificity for P phases. We investigated P speciation across salinity gradients comprising diverse ecosystems in a P-enriched estuary. To determine P load effects on P speciation we compared the high P site with a low P site. Octacalcium phosphate (OCP), authigenic apatite (carbonate fluorapatite, CFAP) and detrital apatite (fluorapatite) were quantitated in addition to Al/Fe-bound P (Al/Fe-P) and Ca-bound P (Ca-P). Gradients in sediment pH strongly affected P fractions across ecosystems and independent of the site-specific total P status. We found a pronounced switch from adsorbed Al/Fe-P to mineral Ca-P with decreasing acidity from land to sea. This switch occurred at near-neutral sediment pH and has possibly been enhanced by redox-driven phosphate desorption from iron oxyhydroxides. The seaward decline in Al/Fe-P was counterbalanced by the precipitation of Ca-P. Correspondingly, two location-dependent accumulation mechanisms occurred at the high P site due to the switch, leading to elevated Al/Fe-P at pH < 6.6 (landward; adsorption) and elevated Ca-P at pH > 6.6 (seaward; precipitation). Enhanced Ca-P precipitation by increased P loads was also evident from disproportional accumulation of metastable Ca-P (Ca-Pmeta) at the high P site. Here, sediments contained on average 6-fold higher Ca-Pmeta levels compared with the low P site, although these sediments contained only 2-fold more total Ca-P than the low P sediments. Phosphorus species distributions indicated that these elevated Ca-Pmeta levels resulted from transformation of fertilizer-derived Al/Fe-P to OCP and CFAP in nearshore areas. Formation of CFAP as well as its precursor, OCP, results in P retention in coastal zones and can thus lead to substantial inorganic P accumulation in response to anthropogenic P input.

  4. Vacuum-sintered body of a novel apatite for artificial bone

    NASA Astrophysics Data System (ADS)

    Tamura, Kenichi; Fujita, Tatsushi; Morisaki, Yuriko

    2013-12-01

    We produced regenerative artificial bone material and bone parts using vacuum-sintered bodies of a novel apatite called "Titanium medical apatite (TMA®)" for biomedical applications. TMA was formed by chemically connecting a Ti oxide molecule with the reactive [Ca10(PO4)6] group of Hydroxyapatite (HAp). The TMA powders were kneaded with distilled water, and solid cylinders of compacted TMA were made by compression molding at 10 MPa using a stainless-steel vessel. The TMA compacts were dried and then sintered in vacuum (about 10-3 Pa) or in air using a resistance heating furnace in the temperature range 1073-1773 K. TMA compacts were sintered at temperatures greater than 1073 K, thus resulting in recrystallization. The TMA compact bodies sintered in the range 1273-1773 K were converted into mixtures composed of three crystalline materials: α-TCP (tricalcium phosphate), β-TCP, and Perovskite-CaTiO3. The Perovskite crystals were stable and hard. In vacuum-sintering, the Perovskite crystals were transformed into fibers (approximately 1 µm in diameter × 8 µm in length), and the fiber distribution was uniform in various directions. We refer to the TMA vacuum-sintered bodies as a "reinforced composite material with Perovskite crystal fibers." However, in atmospheric sintering, the Perovskite crystals were of various sizes and were irregularly distributed as a result of the effect of oxygen. After sintering temperature at 1573 K, the following results were obtained: the obtained TMA vacuum-sintered bodies (1) were white, (2) had a density of approximately 2300 kg/m3 (corresponding to that of a compact bone or a tooth), and had a thermal conductivity of approximately 31.3 W/(m·K) (corresponding to those of metal or ceramic implants). Further, it was possible to cut the TMA bodies into various forms with a cutting machine. An implant made of TMA and inserted into a rabbit jaw bone was covered by new bone tissues after just one month because of the high

  5. Strontium ranelate changes the composition and crystal structure of the biological bone-like apatite produced in osteoblast cell cultures.

    PubMed

    Querido, William; Campos, Andrea P C; Martins Ferreira, Erlon H; San Gil, Rosane A S; Rossi, Alexandre M; Farina, Marcos

    2014-09-01

    We evaluate the effects of strontium ranelate on the composition and crystal structure of the biological bone-like apatite produced in osteoblast cell cultures, a system that gave us the advantage of obtaining mineral samples produced exclusively during treatment. Cells were treated with strontium ranelate at concentrations of 0.05 and 0.5 mM Sr(2+). Mineral substances were isolated and analyzed by using a combination of methods: Fourier transform infrared spectroscopy, solid-state (1)H nuclear magnetic resonance, X-ray diffraction, micro-Raman spectroscopy and energy dispersive X-ray spectroscopy. The minerals produced in all cell cultures were typical bone-like apatites. No changes occurred in the local structural order or crystal size of the minerals. However, we noticed several relevant changes in the mineral produced under 0.5 mM Sr(2+): (1) increase in type-B CO3 (2-) substitutions, which often lead to the creation of vacancies in Ca(2+) and OH(-) sites; (2) incorporation of Sr(2+) by substituting slightly less than 10 % of Ca(2+) in the apatite crystal lattice, resulting in an increase in both lattice parameters a and c; (3) change in the PO4 (3-) environments, possibly because of the expansion of the lattice; (4) the Ca/P ratio of this mineral was reduced, but its (Ca+Sr)/P ratio was the same as that of the control, indicating that its overall cation/P ratio was preserved. Thus, strontium ranelate changes the composition and crystal structure of the biological bone-like apatite produced in osteoblast cell cultures. PMID:24859219

  6. Carbonatite melt inclusions in coexisting magnetite, apatite and monticellite in Kerimasi calciocarbonatite, Tanzania: melt evolution and petrogenesis

    NASA Astrophysics Data System (ADS)

    Guzmics, Tibor; Mitchell, Roger H.; Szabó, Csaba; Berkesi, Márta; Milke, Ralf; Abart, Rainer

    2011-02-01

    Kerimasi calciocarbonatite consists principally of calcite together with lesser apatite, magnetite, and monticellite. Calcite hosts fluid and S-bearing Na-K-Ca-carbonate inclusions. Carbonatite melt and fluid inclusions occur in apatite and magnetite, and silicate melt inclusions in magnetite. This study presents statistically significant compositional data for quenched S- and P-bearing, Ca-alkali-rich carbonatite melt inclusions in magnetite and apatite. Magnetite-hosted silicate melts are peralkaline with normative sodium-metasilicate. On the basis of our microthermometric results on apatite-hosted melt inclusions and forsterite-monticellite phase relationships, temperatures of the early stage of magma evolution are estimated to be 900-1,000°C. At this time three immiscible liquid phases coexisted: (1) a Ca-rich, P-, S- and alkali-bearing carbonatite melt, (2) a Mg- and Fe-rich, peralkaline silicate melt, and (3) a C-O-H-S-alkali fluid. During the development of coexisting carbonatite and silicate melts, the Si/Al and Mg/Fe ratio of the silicate melt decreased with contemporaneous increase in alkalis due to olivine fractionation, whereas the alkali content of the carbonatite melt increased with concomitant decrease in CaO resulting from calcite fractionation. Overall the peralkalinity of the bulk composition of the immiscible melts increased, resulting in a decrease in the size of the miscibility gap in the pseudoquaternary system studied. Inclusion data indicate the formation of a carbonatite magma that is extremely enriched in alkalis with a composition similar to that of Oldoinyo Lengai natrocarbonatite. In contrast to the bulk compositions of calciocarbonatite rocks, the melt inclusions investigated contain significant amount of alkalis (Na2O + K2O) that is at least 5-10 wt%. The compositions of carbonatite melt inclusions are considered as being better representatives of parental magma composition than those of any bulk rock.

  7. The possibility of the formation of protocells and their structural components on the basis of the apatite matrix and cocrystallizing minerals.

    PubMed

    Kostetsky, Eduard Y

    2005-12-01

    This paper presents the author's theory on the possibility of simultaneous hard-phase synthesis of various organic molecules from gas-phase elements on the basis of the apatite matrix and cocrystallizing minerals (carbonate-apatite, calcite, mica). These molecules and their ensembles gave rise to living systems and protocells of the pro- and eukaryotic types. Synthesis might have occurred through gradual substitution of the mineral matrix by crystal organic matter. The structure and size of the molecules synthesized were determined by the structure, physical parameters, and arrangement of organizing centers in the crystal lattice. Apatite phosphates were embedded in a synthesized nucleic helix and their size and purine-pyrimidine complementarity were determined. Apatite and cocrystallizing minerals were seen to be involved in the synthesis of four basic classes of cell components: apatite-DNA and nucleoproteide complexes; carbonate-apatite-enzymes, other proteins involved in DNA replication, all RNA types and their complexes with the specific proteins and enzymes of transcription and translation; calcite-cytoskeletal proteins; and mica-membrane lipids and proteins. The evidence supporting this theory is presented. A possible mechanism to account for the transition from crystal through organo-mineral crystal to liquid crystal (protocell) and a model of the occurrence of the matrix mechanism of transcription and translation are proposed. Some principal problems in the biochemistry and molecular biology of the origin of life on the Earth are discussed. PMID:23345922

  8. Inhibition of precipitation of carbonate apatite by trisodium citrate analysed in base of the formation of chemical complexes in growth solution

    NASA Astrophysics Data System (ADS)

    Prywer, Jolanta; Olszynski, Marcin; Mielniczek-Brzóska, Ewa

    2015-11-01

    Effect of trisodium citrate on the precipitation of carbonate apatite is studied. The experimental series are performed in the solution of artificial urine. The investigations are related to infectious urinary stones formation as carbonate apatite is one of the main components of this kind of stones. To mimic a real infection in urinary tract the aqueous ammonia solution was added to the solution of artificial urine. The spectrophotometric results demonstrate that trisodium citrate increases induction time with respect to carbonate apatite formation and decreases the efficiency of carbonate apatite precipitation. The inhibitory effect of trisodium citrate on the precipitation of carbonate apatite is explained in base of chemical speciation analysis. Such an analysis demonstrates that the inhibitory effect is mainly related with the fact that trisodium citrate binds Ca2+ ions and causes the formation of CaCit- and Ca10(PO4)6CO3 complexes. Trisodium citrate binds Ca2+ ions in the range of pH from 6 to 9.5 for which carbonate apatite is favored to be formed.

  9. Effect of calcium salt content in the poly(epsilon-caprolactone)/silica nanocomposite on the nucleation and growth behavior of apatite layer.

    PubMed

    Rhee, Sang-Hoon

    2003-12-15

    The effect of calcium salt content in the poly(epsilon-caprolactone) (PCL)/silica nanocomposite on the nucleation and growth behavior of apatite layer in simulated body fluid (SBF) was investigated. The specimens were prepared with low (L) and high (H) concentrations of calcium nitrate tetrahydrate through a sol-gel method. After soaking in the SBF at 36.5 degrees C for 1 week, a densely packed apatite layer that had a smooth surface and a Ca/P ratio similar to bone was formed on specimens containing a low concentration of calcium salt while a loosely packed apatite layer with a rugged surface and a higher Ca/P ratio than that of bone occurred on specimens containing a high concentration of calcium salt. The results are explained in terms of the degree of supersaturation of apatite in the SBF, as determined by the concentrations of constituent ions of apatite and pH. The practical implication of the results is that a dense and bone-like apatite layer on the PCL/silica nanocomposite in vitro, and perhaps in vivo, can be achieved by adopting an appropriate calcium salt content. PMID:14624498

  10. On the mechanism of apatite-induced precipitation on 45S5 glass pellets coated with a natural-derived polymer

    NASA Astrophysics Data System (ADS)

    Araújo, Marco; Miola, Marta; Bertone, Elisa; Baldi, Giovanni; Perez, Javier; Verné, Enrica

    2015-10-01

    In this work, the bioactive glass 45S5 (also known by its commercial name Bioglass®) was successfully dip-coated by a natural derived biopolymer, increasing its apatite-forming ability. The biopolymer was shown to accelerate the first stages of bioactivity, inducing a fast transition to step 4 (formation of amorphous Casbnd P layer) in the apatite-forming ability mechanism. The faster precipitation of Ca/P crystals in the coated samples resulted in the formation of an intermediate amorphous octacalcium phosphate, which later transforms into an apatite layer with high thickness. The effect of the thickness of the coating was also studied on samples coated with polymer suspensions of different concentrations (0.15% and 1.5%, w/v), revealing that the kinetics of formation of the final hydroxycarbonate apatite layer increases with the thickness of the coating. The mechanism by which this apatite-forming ability is accelerated was also investigated, revealing that certain functional groups present in the structure of the polymer allow it to act as an organic matrix and preferential nucleation site for the growth of the hydroxycarbonate apatite layer.

  11. Effect of geometrical structure on drug release rate of a three-dimensionally perforated porous apatite/collagen composite cement.

    PubMed

    Otsuka, Makoto; Nakagawa, Hidenori; Ito, Atsuo; Higuchi, William I

    2010-01-01

    To improve the biocompatibility, inter-connective pore structure, and drug delivery ability of self-setting apatite/collagen composite cement (ACC), a three-dimensionally perforated porous apatite/collagen composite cement (TPPACC) containing 3% indomethacin (IMC) was obtained in an arranged multi-cross with 20, 40, and 60 stainless steel needlelike male dies, and stored and hardened at 37 degrees C and 100% relative humidity for 24 h. The mean radius of micro-pores of the TPPACC was evaluated to be 0.125 microm by mercury porosimetry. X-ray powder diffraction and FT-IR spectroscopy suggested that TPPACC consisted of carbonated apatite and had a structure similar to that of natural rat bone. The IMC release rates from a TPPACC block containing the drug were measured in simulated body fluid. The rate of release increased with the number of macro-pores that from planar surface matrix systems followed the Higuchi equation. The relationship between the Higuchi constant and surface area of TPPACC showed a straight line with K = 0.2123 and R(2) = 0.9892. These results indicated that the rate of drug release from TPPACC could be controlled by the number of macro-pores for bone cells. PMID:19821491

  12. Ca L2,3-edge XANES and Sr K-edge EXAFS study of hydroxyapatite and fossil bone apatite

    NASA Astrophysics Data System (ADS)

    Zougrou, I. M.; Katsikini, M.; Brzhezinskaya, M.; Pinakidou, F.; Papadopoulou, L.; Tsoukala, E.; Paloura, E. C.

    2016-08-01

    Upon burial, the organic and inorganic components of hard tissues such as bone, teeth, and tusks are subjected to various alterations as a result of interactions with the chemical milieu of soil, groundwater, and presence of microorganisms. In this study, simulation of the Ca L 2,3-edge X-ray absorption near edge structure (XANES) spectrum of hydroxyapatite, using the CTM4XAS code, reveals that the different symmetry of the two nonequivalent Ca(1) and Ca(2) sites in the unit cell gives rise to specific spectral features. Moreover, Ca L 2,3-edge XANES spectroscopy is applied in order to assess variations in fossil bone apatite crystallinity due to heavy bacterial alteration and catastrophic mineral dissolution, compared to well-preserved fossil apatite, fresh bone, and geologic apatite reference samples. Fossilization-induced chemical alterations are investigated by means of Ca L 2,3-edge XANES and scanning electron microscopy (SEM) and are related to histological evaluation using optical microscopy images. Finally, the variations in the bonding environment of Sr and its preference for substitution in the Ca(1) or Ca(2) sites upon increasing the Sr/Ca ratio is assessed by Sr K-edge extended X-ray absorption fine structure (EXAFS) spectroscopy.

  13. The structure, bond strength and apatite-inducing ability of micro-arc oxidized tantalum and their response to annealing

    NASA Astrophysics Data System (ADS)

    Wang, Cuicui; Wang, Feng; Han, Yong

    2016-01-01

    In this study, the tantalum oxide coatings were formed on pure tantalum (Ta) by micro-arc oxidation (MAO) in electrolytic solutions of calcium acetate and β-glycerophosphate disodium, and the effect of the applied voltage on the microstructure and bond strength of the MAO coatings was systematically investigated. The effect of annealing treatment on the microstructure, bond strength and apatite-inducing ability of the MAO coatings formed at 350 and 450 V was also studied. The study revealed that during the preparation of tantalum oxide coatings on Ta substrate by MAO, the applied voltage considerably affected the phase components, morphologies and bond strength of the coatings, but had little effect on surface chemical species. After annealing treatment, newly formed CaTa4O11 phase mainly contributed to the much more stronger apatite-inducing ability of the annealed tantalum oxide coatings than those that were not annealed. The better apatite-inducing ability of the MAO coatings formed at 450 V compared to those formed at 350 V was attributed to the less amorphous phase and more crystalline phase as well as more Ca and P contained in the MAO coatings with increasing the applied voltage.

  14. Revisiting the localization of Zn2+ cations sorbed on pathological apatite calcifications made through X-ray absorption spectroscopy

    SciTech Connect

    Bazin, D.; Carpentier, X.; Brocheriou, I.; Dorfmuller, P.; Aubert, S.; Chappard, C.; Thiaudiere, D.; Reguer, S.; Waychunas, G.; Jungers, P.; Daudon, M.

    2009-04-01

    The role of oligo-elements such as Zn in the genesis of pathological calcifications is widely debated in the literature. An essential element of discussion is given by their localization either at the surface or within the Ca apatite crystalline network. To determine the localization, X-ray absorption experiments have been performed at SOLEIL. The Exafs results suggest that Zn atoms, present in the Zn{sup 2+} form, are bound to about 4 O atoms at a distance of 2.00{angstrom}, while the interatomic distance R{sub CaO} ranges between 2.35 {angstrom} and 2.71 {angstrom}. Taking into account the content of Zn (around 1000 ppm) and the difference in ionic radius between Zn{sup 2+} (0.074 nm) and Ca{sup 2+} (0.099 nm), a significant longer interatomic distance would be expected in the case of Zn replacing Ca within the apatite crystalline network. We thus conclude that Zn atoms are localized at the surface and not in the apatite nanocrystal structure. Such structural result has essential biological implications for at least two reasons. Some oligoelements have a marked effect on the transformation of chemical phases, and may modify the morphology of crystals. These are both major issues because, in the case of kidney stones, the medical treatment depends strongly on the precise chemical phase and on the morphology of the biological entities at both macroscopic and mesoscopic scales.

  15. Apatite ore mine tailings as an amendment for remediation of a lead-contaminated shooting range soil.

    PubMed

    Venäläinen, Salla H

    2011-10-01

    This study investigated the use of tailings from apatite ore beneficiation in the remediation of a heavily contaminated shooting range soil. The tailings originating in Siilinjärvi carbonatite complex, Finland, consist of apatite residues accompanied by phlogopite and calcite. In a pot experiment, organic top layer of a boreal forest soil predisposed to pellet-derived lead (Pb) was amended with tailings of various particle-sizes (Ø>0.2mm, Ø<0.2mm and unsieved material) differing in their mineralogical composition. After 9-, 10-, 14- and 21-month incubation, the samples were monitored for tailings-induced changes in the different Pb pools by means of sequential fractionation. Following the incubation, the samples were extracted with water and the extracts were analyzed for Pb species distribution by means of a cation exchange resin. The results revealed that Pb was continuously released from the shotgun pellet fragments due to weathering. However, the apatite and calcite compartments in the tailings counteracted the mobility of the released Pb through the formation of sparingly soluble fluorpyromorphite and cerussite. Furthermore, the tailings efficiently reduced the bioavailability of Pb by transferring it from the water-soluble and exchangeable pools into the organic one. The material also increased the proportion of the less toxic non-cationic Pb to the total dissolved Pb from the initial level of 5% to 9-12%. The results suggest that the tailings-induced stabilization of Pb may be an environmentally sound remediation technique at polluted sites. PMID:21871651

  16. Ca L2,3-edge XANES and Sr K-edge EXAFS study of hydroxyapatite and fossil bone apatite.

    PubMed

    Zougrou, I M; Katsikini, M; Brzhezinskaya, M; Pinakidou, F; Papadopoulou, L; Tsoukala, E; Paloura, E C

    2016-08-01

    Upon burial, the organic and inorganic components of hard tissues such as bone, teeth, and tusks are subjected to various alterations as a result of interactions with the chemical milieu of soil, groundwater, and presence of microorganisms. In this study, simulation of the Ca L 2,3-edge X-ray absorption near edge structure (XANES) spectrum of hydroxyapatite, using the CTM4XAS code, reveals that the different symmetry of the two nonequivalent Ca(1) and Ca(2) sites in the unit cell gives rise to specific spectral features. Moreover, Ca L 2,3-edge XANES spectroscopy is applied in order to assess variations in fossil bone apatite crystallinity due to heavy bacterial alteration and catastrophic mineral dissolution, compared to well-preserved fossil apatite, fresh bone, and geologic apatite reference samples. Fossilization-induced chemical alterations are investigated by means of Ca L 2,3-edge XANES and scanning electron microscopy (SEM) and are related to histological evaluation using optical microscopy images. Finally, the variations in the bonding environment of Sr and its preference for substitution in the Ca(1) or Ca(2) sites upon increasing the Sr/Ca ratio is assessed by Sr K-edge extended X-ray absorption fine structure (EXAFS) spectroscopy. PMID:27379398

  17. In vitro mineralization of bioresorbable poly(ɛ-caprolactone)/apatite composites for bone tissue engineering: a vibrational and thermal investigation

    NASA Astrophysics Data System (ADS)

    Taddei, Paola; Tinti, Anna; Reggiani, Matteo; Fagnano, Concezio

    2005-06-01

    This study was aimed at evaluating the physico-chemical properties of a porous poly(ɛ-caprolactone)/carbonated-apatite (PCL/CAp 30/70 w/w) composite to be used as scaffold for bone tissue engineering. The in vitro degradation mechanism of this matrix in different media was evaluated as well as its bioactivity in a simulated body fluid (SBF) buffered at pH 7.4 (37 °C, 28 days). For this purpose, we used vibrational IR and Raman spectroscopy coupled to thermogravimetry (TG) and differential scanning calorimetry (DSC). The samples were analyzed before and after immersion in the above mentioned solution as well as in 0.01 M NaOH solution (pH=12), saline phosphate buffer at pH 7.4 (SPB) and esterase/SPB. A control PCL sample was analyzed before the addition of the apatitic component. As regards the untreated samples, the method of synthesis utilized for preparing the composite was found to lower the crystallinity degree. The CAp component revealed to be constituted of a B-type CAp with a 3% carbonate content. After immersion in SBF solution, vibrational analysis coupled to TG revealed the deposition of a significant amount of an apatite component on the surface of the PCL/CAp composite as well as in its interior, showing a good in vitro mineralization.

  18. δ18O of apatite phosphate in small pelagic fish: insights from wild-caught and tank-grown specimens

    NASA Astrophysics Data System (ADS)

    Lambert, T.; Javor, B.; Paytan, A.

    2011-12-01

    Oxygen isotope ratios of mineralized structures in fish reflect the temperature and isotopic composition of the water in which they grow. For bulk samples (e.g., whole scales, bones, and otoliths), understanding how this signal is integrated across time and space is critical, especially for organisms exposed to high variability in growth conditions. Here, we assess the response of fish scale δ18O (from apatite phosphate) to experimentally manipulated water conditions. Wild-caught sardines were grown at controlled temperatures (13°C, 17°C, and 21°C) for 11 months. Higher growth temperatures correlated to lower δ18O values, representing a combination of scale apatite deposited before and after the temperature manipulation. Models that account for both biomineral allometry and exposure to varying water properties (e.g., by overlaying migration routes, isoscapes, and temperature maps) have the potential to quantify the varying contributions of minerals grown under different conditions. We use this method to predict δ18O of apatite phosphate for small pelagic fish found in California coastal waters, then compare expected values to those obtained from collected samples. Since phosphate oxygen is relatively resistant to diagenesis, this modern calibration establishes a framework for paleo studies.

  19. Apatite, SiO2, rutile and orthopyroxene precipitates in minerals of eclogite xenoliths from Yakutian kimberlites, Russia

    NASA Astrophysics Data System (ADS)

    Alifirova, T. A.; Pokhilenko, L. N.; Korsakov, A. V.

    2015-06-01

    Eclogite mantle xenoliths from the central part of Siberian craton (Udachnaya and Zarnitsa kimberlite pipes) as well as from the northeastern edge of the craton (Obnazhennaya kimberlite) were studied in detail. Garnet and clinopyroxene show evident exsolution textures. Garnet comprises rutile, ilmenite, apatite, and quartz/coesite oriented inclusions. Clinopyroxene contains rutile (± ilmenite) and apatite precipitates. Granular inclusions of quartz in kyanite and garnet usually retain features of their high-pressure origin. According to thermobarometric calculations, the studied eclogitic suite was equilibrated within lithospheric mantle at 3.2-4.9 GPa and 813-1080 °C. The precursor composition of garnets from Udachnaya and Zarnitsa eclogites suggests their stability at depths 210-260 km. Apatite precipitation in clinopyroxenes of Udachnaya and Zarnitsa allows us to declare that original pyroxenes could have been indicative of their high P-T stability. Raman spectroscopic study of quartz and coesite precipitates in garnet porphyroblasts confirms our hypothesis on the origin of the exsolution textures during pressure-temperature decrease. With respect to mineralogical data, we suppose the rocks to be subjected to stepwise decompression and cooling within mantle reservoir.

  20. Quinone-rich polydopamine functionalization of yttria stabilized zirconia for apatite biomineralization: The effects of coating temperature

    NASA Astrophysics Data System (ADS)

    Zain, Norhidayu Muhamad; Hussain, Rafaqat; Abdul Kadir, Mohammed Rafiq

    2015-08-01

    The use of yttria stabilized zirconia (YSZ) as biomedical implants is often offset by its bioinert nature that prevents its osseointegration to occur. Therefore, the functionalization of YSZ surface by polydopamine to facilitate the biomineralization of apatite layer on top of the coated film has incessantly been studied. In this study YSZ discs were first immersed in 2 mg/mL of stirred dopamine solution at coating temperatures between 25 and 80 °C. The specimens were then incubated for 7d in 1.5 SBF. The effect of coating temperature on the properties (chemical compositions and wettability) and the apatite mineralization on top of the generated films was investigated. It was found that at 50 °C, the specimen displayed the highest intensity of Ca 2p peak (1.55 ± 0.42 cps) with Ca/P ratio of 1.67 due to the presence of abundant quinone groups (Cdbnd O). However, the hydrophilicity (40.9 ± 01.7°) was greatly improved at 60 °C accompanied by the highest film thickness of 306 nm. Therefore, it was concluded that the presence of high intensity of quinone groups (Cdbnd O) in polydopamine film at elevated temperature affects the chelation of Ca2+ ions and thus enhance the growth of apatite layer on top of the functionalized YSZ surface.

  1. Feasibility/treatability studies for removal of heavy metals from training range soils at the Grafenwoehr Training Area, Germany

    SciTech Connect

    Peters, R.W.

    1995-05-01

    A feasibility/treatability study was performed to investigate the leaching potential of heavy metals (particularly lead) from soils at the Grafenw6hr Training Area (GTA) in Germany. The study included an evaluation of the effectiveness of chelant extraction to remediate the heavy-metal-contarninated soils. Batch shaker tests indicated that ethylenediaminetetraacetic acid (EDTA) (0.01M) was more effective than citric acid (0.01M) at removing cadmium, copper, lead, and zinc. EDTA and citric acid were equally effective in mobilizing chromium and barium from the soil. The batch shaker technique with chelant extraction offers promise as a remediation technique for heavy-metal-contaninated soil at the GTA. Columnar flooding tests conducted as part of the study revealed that deionized water was the least effective leaching solution for mobilization of the heavy metals; the maximum solubilization obtained was 3.72% for cadmium. EDTA (0.05M) achieved the greatest removal of lead (average removal of 17.6%). The difficulty of extraction using deionized water indicates that all of the heavy metals are very tightly bound to the soil; therefore, they are very stable in the GTA soils and do not pose a serious threat to the groundwater system. Columnar flooding probably does not represent a viable remediation technique for in-situ cleanup of heavy-metal-contaminated soils at the GTA.

  2. Phase 1 report on the Bear Creek Valley treatability study, Oak Ridge Y-12 Plant, Oak Ridge, Tennessee

    SciTech Connect

    1997-04-01

    Bear Creek Valley (BCV) is located within the US Department of Energy (DOE) Oak Ridge Reservation and encompasses multiple waste units containing hazardous and radioactive wastes associated with past operations at the adjacent Oak Ridge Y-12 Plant. The BCV Remedial Investigation determined that disposal of wastes at the S-3 Site, Boneyard/Burnyard (BYBY), and Bear Creek Burial Grounds (BCBG) has caused contamination of both deep and shallow groundwater. The primary contaminants include uranium, nitrate, and VOCs, although other metals such as aluminum, magnesium, and cadmium persist. The BCV feasibility study will describe several remedial options for this area, including both in situ and ex situ treatment of groundwater. This Treatability Study Phase 1 Report describes the results of preliminary screening of treatment technologies that may be applied within BCV. Four activities were undertaken in Phase 1: field characterization, laboratory screening of potential sorbents, laboratory testing of zero valent iron products, and field screening of three biological treatment systems. Each of these activities is described fully in technical memos attached in Appendices A through G.

  3. Portraying mental illness and drug addiction as treatable health conditions: effects of a randomized experiment on stigma and discrimination.

    PubMed

    McGinty, Emma E; Goldman, Howard H; Pescosolido, Bernice; Barry, Colleen L

    2015-02-01

    Despite significant advances in treatment, stigma and discrimination toward persons with mental illness and drug addiction have remained constant in past decades. Prior work suggests that portraying other stigmatized health conditions (i.e., HIV/AIDS) as treatable can improve public attitudes toward those affected. Our study compared the effects of vignettes portraying persons with untreated and symptomatic versus successfully treated and asymptomatic mental illness and drug addiction on several dimensions of public attitudes about these conditions. We conducted a survey-embedded randomized experiment using a national sample (N = 3940) from an online panel. Respondents were randomly assigned to read one of ten vignettes. Vignette one was a control vignette, vignettes 2-5 portrayed individuals with untreated schizophrenia, depression, prescription pain medication addiction and heroin addiction, and vignettes 6-10 portrayed successfully treated individuals with the same conditions. After reading the randomly assigned vignette, respondents answered questions about their attitudes related to mental illness or drug addiction. Portrayals of untreated and symptomatic schizophrenia, depression, and heroin addiction heightened negative public attitudes toward persons with mental illness and drug addiction. In contrast, portrayals of successfully treated schizophrenia, prescription painkiller addiction, and heroin addiction led to less desire for social distance, greater belief in the effectiveness of treatment, and less willingness to discriminate against persons with these conditions. Portrayal of persons with successfully treated mental illness and drug addiction is a promising strategy for reducing stigma and discrimination toward persons with these conditions and improving public perceptions of treatment effectiveness. PMID:25528557

  4. Folate Receptor Alpha Defect Causes Cerebral Folate Transport Deficiency: A Treatable Neurodegenerative Disorder Associated with Disturbed Myelin Metabolism

    PubMed Central

    Steinfeld, Robert; Grapp, Marcel; Kraetzner, Ralph; Dreha-Kulaczewski, Steffi; Helms, Gunther; Dechent, Peter; Wevers, Ron; Grosso, Salvatore; Gärtner, Jutta

    2009-01-01

    Sufficient folate supplementation is essential for a multitude of biological processes and diverse organ systems. At least five distinct inherited disorders of folate transport and metabolism are presently known, all of which cause systemic folate deficiency. We identified an inherited brain-specific folate transport defect that is caused by mutations in the folate receptor 1 (FOLR1) gene coding for folate receptor alpha (FRα). Three patients carrying FOLR1 mutations developed progressive movement disturbance, psychomotor decline, and epilepsy and showed severely reduced folate concentrations in the cerebrospinal fluid (CSF). Brain magnetic resonance imaging (MRI) demonstrated profound hypomyelination, and MR-based in vivo metabolite analysis indicated a combined depletion of white-matter choline and inositol. Retroviral transfection of patient cells with either FRα or FRβ could rescue folate binding. Furthermore, CSF folate concentrations, as well as glial choline and inositol depletion, were restored by folinic acid therapy and preceded clinical improvements. Our studies not only characterize a previously unknown and treatable disorder of early childhood, but also provide new insights into the folate metabolic pathways involved in postnatal myelination and brain development. PMID:19732866

  5. Curable or treatable? The implications of different definitions of illness when treating patients suffering from amyotrophic lateral sclerosis.

    PubMed

    Cappellato, Valeria; Bosco, Nicoletta; Chiò, Adriano; Calvo, Andrea

    2015-01-01

    People suffering from amyotrophic lateral sclerosis (ALS) have complex health and care needs. The purpose of this study was to gain insight into the gaps in the health and community service care provided to ALS patients. In order to ensure continuity of care, specialist centres have to build effective relationships with local primary health care services and community services, health managers, physicians, patients, families and the surrounding support networks. We undertook a qualitative study that examined the specialist centres in hospitals, communities and primary care services. In 2010 we carried out 47 semi-structured interviews and one group interview in Italy, targeting all those involved in ALS care, on all levels. We used purposive sampling to obtain maximum variation across professions, sectors and services. Participants reported gaps arising when local health managers have to assess patient eligibility for certain services. The need to set priorities when allocating resources means that professionals 'categorize' patients without considering the multidimensional nature of their needs. For instance, rehabilitation is generally guaranteed for people with temporary or non-progressive functional limitations, yet it is not granted to degenerative patients. Patients with similar physical conditions, with perceived differences of other kinds (i.e. curable vs. treatable), may experience differential access to care. PMID:26467979

  6. Seasonal variation of organic matter concentration and characteristics in the Maji ya Chai River (Tanzania): Impact on treatability by ultrafiltration.

    PubMed

    Aschermann, Geert; Jeihanipour, Azam; Shen, Junjie; Mkongo, Godfrey; Dramas, Laure; Croué, Jean-Philippe; Schäfer, Andrea

    2016-09-15

    Many waters in Tanzania exhibit high concentrations of organic matter and dissolved contaminants such as fluoride. Due to bacteria and virus removal, ultrafiltration (UF) is an attractive option for drinking water treatment, and when coupled with adsorbents, may compete with other established processes like nanofiltration (NF) for lower contaminant concentrations. The results presented here examine the characteristics and treatability of tropical natural organic matter (NOM) by UF as a function of seasonal variation. The Tanzanian river Maji ya Chai was sampled monthly during one year. The composition of NOM in Maji ya Chai River is influenced strongly by precipitation. Total organic carbon (TOC), specific ultraviolet absorbance (SUVA) and concentration of allochthonous organics substances (such as humic substances (HS)) are elevated in periods following high precipitation, while TOC is lower and contains more biopolymers in the dry seasons. UF experiments with two regenerated cellulose membranes of different molecular weight cut-off (MWCO, 5 and 10 kDa) were conducted. UF is able to remove 50-95% of TOC with a seasonal variability of 10-20%. Due to the remaining NOM in the water that would contribute to disinfection by-product formation and bacterial regrowth, the physically disinfected water is more applicable for point of use systems than distribution or storage. PMID:27288671

  7. Portraying Mental Illness and Drug Addiction as Treatable Health Conditions: Effects of a Randomized Experiment on Stigma and Discrimination

    PubMed Central

    Goldman, Howard H.; Pescosolido, Bernice; Barry, Colleen L.

    2016-01-01

    Despite significant advances in treatment, stigma and discrimination toward persons with mental illness and drug addiction have remained constant in past decades. Prior work suggests that portraying other stigmatized health conditions (i.e., HIV/AIDS) as treatable can improve public attitudes toward those affected. Our study compared the effects of vignettes portraying persons with untreated and symptomatic versus successfully treated and asymptomatic mental illness and drug addiction on several dimensions of public attitudes about these conditions. We conducted a survey-embedded randomized experiment using a national sample (N=3940) from an online panel. Respondents were randomly assigned to read one of ten vignettes. Vignette one was a control vignette, vignettes 2–5 portrayed individuals with untreated schizophrenia, depression, prescription pain medication addiction and heroin addiction, and vignettes 6–10 portrayed successfully treated individuals with the same conditions. After reading the randomly assigned vignette, respondents answered questions about their attitudes related to mental illness or drug addiction. Portrayals of untreated and symptomatic schizophrenia, depression, and heroin addiction heightened negative public attitudes toward persons with mental illness and drug addiction. In contrast, portrayals of successfully treated schizophrenia, prescription painkiller addiction, and heroin addiction led to less desire for social distance, greater belief in the effectiveness of treatment, and less willingness to discriminate against persons with these conditions. Portrayal of persons with successfully treated mental illness and drug addiction is a promising strategy for reducing stigma and discrimination toward persons with these conditions and improving public perceptions of treatment effectiveness. PMID:25528557

  8. Metallurgical Laboratory (MetLab) Treatability Study: An Analysis of Passive Soil Vapor Extraction Wells (PSVE) FY1999 Update

    SciTech Connect

    Riha, B.D.

    1999-10-20

    The results to date on the treatability study of the PSVE system at the MetLab of the Savannah River Site (SRS) indicate the technology is performing well. Well concentrations are decreasing and contour maps of the vadose zone soil gas plume show a decrease in the extent of the plume. In the 18 months of operation approximately 200 pounds of chlorinated organic contaminants have been removed by natural barometric pumping of wells fitted with BaroBall valves (low pressure check valves). The mass removal estimates are approximate since the flow rates are estimated, the concentration data is based on exponential fits of a limited data set, and the concentration data is normalized to the average CO2.The concentration values presented in this report should be taken as the general trend or order of magnitude of concentration until longer-term data is collected. These trends are of exponentially decreasing concentration showing the same characteristics as the concentration trends at the SRS Miscellaneous Chemical Basin after three years of PSVE (Riha et. al., 1999).

  9. Bone tissue reactions to biomimetic ion-substituted apatite surfaces on titanium implants

    PubMed Central

    Ballo, Ahmed M.; Xia, Wei; Palmquist, Anders; Lindahl, Carl; Emanuelsson, Lena; Lausmaa, Jukka; Engqvist, Håkan; Thomsen, Peter

    2012-01-01

    The aim of this study was to evaluate the bone tissue response to strontium- and silicon-substituted apatite (Sr-HA and Si-HA) modified titanium (Ti) implants. Sr-HA, Si-HA and HA were grown on thermally oxidized Ti implants by a biomimetic process. Oxidized implants were used as controls. Surface properties, i.e. chemical composition, surface thickness, morphology/pore characteristics, crystal structure and roughness, were characterized with various analytical techniques. The implants were inserted in rat tibiae and block biopsies were prepared for histology, histomorphometry and scanning electron microscopy analysis. Histologically, new bone formed on all implant surfaces. The bone was deposited directly onto the Sr-HA and Si-HA implants without any intervening soft tissue. The statistical analysis showed significant higher amount of bone–implant contact (BIC) for the Si-doped HA modification (P = 0.030), whereas significant higher bone area (BA) for the Sr-doped HA modification (P = 0.034), when compared with the non-doped HA modification. The differences were most pronounced at the early time point. The healing time had a significant impact for both BA and BIC (P < 0.001). The present results show that biomimetically prepared Si-HA and Sr-HA on Ti implants provided bioactivity and promoted early bone formation. PMID:22279159

  10. REE partitioning between apatite and melt in a peralkaline volcanic suite, Kenya Rift Valley

    USGS Publications Warehouse

    Macdonald, R.; Baginski, B.; Belkin, H.E.; Dzierzanowski, P.; Jezak, L.

    2009-01-01

    Electron microprobe analyses are presented for fluorapatite phenocrysts from a benmoreite-peralkaline rhyolite volcanic suite from the Kenya Rift Valley. The rocks have previously been well characterized petrographically and their crystallization conditions are reasonably well known. The REE contents in the M site increase towards the rhyolites, with a maximum britholite component of ~35 mol.%. Chondrite-normalized REE patterns are rather flat between La and Sm and then decrease towards Yb. Sodium and Fe occupy up to 1% and 4%, respectively, of the M site. The major coupled substitution is REE3+ + Si4+ ??? Ca2+ + P5+. The substitution REE3+ + Na+ ??? 2Ca2+ has been of minor importance. The relatively large Fe contents were perhaps facilitated by the low fo2 conditions of crystallization. Zoning is ubiquitous and resulted from both fractional crystallization and magma mixing. Apatites in some rhyolites are relatively Y-depleted, perhaps reflecting crystallization from melts which had precipitated zircon. Mineral/glass (melt) ratios for two rhyolites are unusually high, with maxima at Sm (762, 1123). ?? 2008 The Mineralogical Society.

  11. Possible Roles of Fluoride and Carbonate in Biochemical Carbonated Apatite Formation

    NASA Astrophysics Data System (ADS)

    Meouch, Orysia; Omelon, Sidney

    2016-04-01

    Marine phosphorites are predominantly composed of carbonated fluorapatite (CFA = Ca10‑a‑b‑cNaaMgb(PO4)6‑x(CO3)x‑y‑z(CO3.F)y(SO4)zF2, where x=y+a+2c, and c represents the number of Ca vacancies, with a P2O5 content that ranges from 18-40 %. Sulphur-oxidizing bacteria of the Beggiatoa genus concentration phosphorous as intracellular polyphosphate ((PO3‑)n) which is depolymerized into inorganic orthophosphate (Pi). Consequently, an increase in pore water Pi concentration favours carbonated apatite precipitation. The carbonate and fluoride that is characteristic of phosphorite CFA is also located in the vertebrate skeleton. This similarity suggests a biochemical pathway for CFA precipitation. Preliminary Raman spectroscopy and powder x-ray diffraction results that suggest a role for fluoride, and possibly carbonate, in the biochemical depolymerisation of polyphosphates with alkaline phosphatase will be presented.

  12. Osteointegration of biomimetic apatite coating applied onto dense and porous metal implants in femurs of goats.

    PubMed

    Barrère, F; van der Valk, C M; Meijer, G; Dalmeijer, R A J; de Groot, K; Layrolle, P

    2003-10-15

    Biomimetic calcium phosphate (Ca-P) coatings were applied onto dense titanium alloy (Ti6Al4V) and porous tantalum (Ta) cylinders by immersion into simulated body fluid at 37 degrees C and then at 50 degrees C for 24 h. As a result, a homogeneous bone-like carbonated apatitic (BCA) coating, 30 microm thick was deposited on the entire surface of the dense and porous implants. Noncoated and BCA-coated implants were press-fit implanted in the femoral diaphysis of 14 adult female goats. Bone contact was measured after implantation for 6, 12, and 24 weeks, and investigated by histology and backscattered electron microscopy (BSEM). After 6 weeks, bone contact of the BCA-coated Ti6Al4V implants was about 50%. After 12 and 24 weeks, bone contact was lower in comparison with the 6-week implantations at, respectively 24 and 39%. Regarding the BCA-coated porous Ta implants, bone contacts were 17, 30, and 18% after 6, 12, and 24 weeks, respectively. However, bone contact was always found significantly higher for BCA-coated dense Ti6Al4V and porous Ta cylinders than the corresponding noncoated implants. The results of this study show that the BCA coating enhances the bone integration as compared to the noncoated implants. PMID:14528464

  13. Evaluation of strontium introduced apatite cement as the injectable bone substitute developments.

    PubMed

    Sekine, Kazumitsu; Sakama, Minoru; Hamada, Kenichi

    2013-01-01

    We have developed bone cement introducing Strontium (Sr) to promote early bone regeneration. To prolong the release duration of Sr, we applied inorganic Sr filler for containing into the cement powder. The purpose of this study is to evaluate the mechanical properties, crystallinic properties, and ion release activities, especially Sr anion, of this cement. Alpha-TCP powder was mixed with Sr filler, with 0.1wt%, 0.5wt%, 1.0wt%, and 5.0wt%. These were mixed with mixing liquid and formed for each test. They were incubated and crystalized in 95% moisture for 1 week. The mechanical properties were studied by the compression, the diametral tensile strength and 4-point vending. Tested specimens were evaluated by X-ray diffraction(XRD) and scanning electron microscopic(SEM) imaging. The ion release behaviors were measured by inductively coupled plasma mass spectrometry(ICP-MS). The mechanical properties were increased in consistency of filler, but decreased in some samples because of declining the apatite matrix. And the Sr release showed interesting results as the sequential resource of Sr. By adjusting the mixing ratio or considering the application of these Sr releasable cements, this material would show good performance by its strength and longer Sr release for bone regeneration. PMID:24109823

  14. Extraction and characterisation of apatite- and tricalcium phosphate-based materials from cod fish bones.

    PubMed

    Piccirillo, C; Silva, M F; Pullar, R C; Braga da Cruz, I; Jorge, R; Pintado, M M E; Castro, P M L

    2013-01-01

    Apatite- and tricalcium phosphate-based materials were produced from codfish bones, thus converting a waste by-product from the food industry into high added-valued compounds. The bones were annealed at temperatures between 900 and 1200 °C, giving a biphasic material of hydroxyapatite and tricalcium phosphate (Ca10(PO4)6(OH)2 and β-Ca(PO4)3) with a molar proportion of 75:25, a material widely used in biomedical implants. The treatment of the bones in solution prior to their annealing changed the composition of the material. Single phase hydroxyapatite, chlorapatite (Ca10(PO4)6Cl2) and fluorapatite (Ca10(PO4)6F2) were obtained using CaCl2 and NaF solutions, respectively. The samples were analysed by several techniques (X-ray diffraction, infrared spectroscopy, scanning electron microscopy and differential thermal/thermogravimetric analysis) and by elemental analyses, to have a more complete understanding of the conversion process. Such compositional modifications have never been performed before for these materials of natural origin to tailor the relative concentrations of elements. This paper shows the great potential for the conversion of this by-product into highly valuable compounds for biomedical applications, using a simple and effective valorisation process. PMID:25428050

  15. Apatite-type SrPr(4)(SiO(4))(3)O.

    PubMed

    Sakakura, Terutoshi; Kamoshita, Minami; Iguchi, Hironaga; Wang, Jun; Ishizawa, Nobuo

    2010-01-01

    Single crystals of the title compound, strontium tetra-praseo-dymium tris-(silicate) oxide, SrPr(4)(SiO(4))(3)O, have been grown by the self-flux method using SrCl(2). The structure is isotypic with the apatite supergroup family having the generic formula (IX)M1(2) (VII)M2(3)((IV)TO(4))(3)X, where M = alkaline earth and rare earth metals, T = Si and X = O. The M1 site (3.. symmetry) is occupied by Pr and Sr atoms with almost even proportions and is surrounded by nine O atoms forming a tricapped trigonal prism. The M2 site (m.. symmetry) is almost exclusively occupied by Pr and surrounded by seven O atoms, forming a distorted penta-gonal bipyramid. The Si atom (m.. symmetry) is surrounded by two O (m.. symmetry) and two O atoms in general positions, forming an isolated SiO(4) tetra-hedron. Another O atom at the inversion centre (.. symmetry) is surrounded by three M2 sites, forming an equilateral triangle perpendicular to the c axis. PMID:21588475

  16. Innovative Delivery of siRNA to Solid Tumors by Super Carbonate Apatite

    PubMed Central

    Wu, Xin; Yamamoto, Hirofumi; Nakanishi, Hiroyuki; Yamamoto, Yuki; Inoue, Akira; Tei, Mitsuyoshi; Hirose, Hajime; Uemura, Mamoru; Nishimura, Junichi; Hata, Taishi; Takemasa, Ichiro; Mizushima, Tsunekazu; Hossain, Sharif; Akaike, Toshihiro; Matsuura, Nariaki; Doki, Yuichiro; Mori, Masaki

    2015-01-01

    RNA interference (RNAi) technology is currently being tested in clinical trials for a limited number of diseases. However, systemic delivery of small interfering RNA (siRNA) to solid tumors has not yet been achieved in clinics. Here, we introduce an in vivo pH-sensitive delivery system for siRNA using super carbonate apatite (sCA) nanoparticles, which is the smallest class of nanocarrier. These carriers consist simply of inorganic ions and accumulate specifically in tumors, yet they cause no serious adverse events in mice and monkeys. Intravenously administered sCA-siRNA abundantly accumulated in the cytoplasm of tumor cells at 4 h, indicating quick achievement of endosomal escape. sCA-survivin-siRNA induced apoptosis in HT29 tumors and significantly inhibited in vivo tumor growth of HCT116, to a greater extent than two other in vivo delivery reagents. With innovative in vivo delivery efficiency, sCA could be a useful nanoparticle for the therapy of solid tumors. PMID:25738937

  17. Application of carbonated apatite coating on a Ti substrate by aqueous spray method.

    PubMed

    Mochizuki, Chihiro; Hara, Hiroki; Takano, Ichiro; Hayakawa, Tohru; Sato, Mitsunobu

    2013-03-01

    The fabrication and characterization of a carbonate-containing apatite film deposited on a Ti plate via an aqueous spray method is described. The mist of the spray solution emitted from a perpendicularly oriented airbrush was made to strike a warmed Ti substrate. The thicknesses of the sprayed film and those heat-treated at 400 °C-700 °C under Ar gas flow were in the range 1.21-1.40 μm. The results of elemental analyses and Fourier transform infrared spectroscopy of the powders that were mechanically collected from the surface of the sprayed film suggest that the film was Ca(10)(PO4)6(CO3) · 2CO2 · 3H2O. The presence of the carbonate ion and the lattice CO2 molecule was confirmed via the aforementioned analyses; the finding was also consistent with the X-ray diffraction patterns of the films and the chemical identity of the sprayed and heat-treated films that were measured using X-ray photoelectron spectroscopy. The sprayed film comprises a characteristic network structure, which contains round particles within the networks, as was observed by field-emission scanning electron microscopy. A scratch test indicated that the shear stress of the sprayed film (21 MPa) significantly improved to 40 and >133 MPa after heat-treatment at 600 °C and 700 °C, respectively, under Ar gas flow for 10 min. PMID:25427510

  18. Biomimetic formation of apatite on the surface of porous gelatin/bioactive glass nanocomposite scaffolds

    NASA Astrophysics Data System (ADS)

    Mozafari, Masoud; Rabiee, Mohammad; Azami, Mahmoud; Maleknia, Saied

    2010-12-01

    There have been several attempts to combine bioactive glasses (BaGs) with biodegradable polymers to create a scaffold material with excellent biocompatibility, bioactivity, biodegradability and toughness. In the present study, the nanocomposite scaffolds with compositions based on gelatin (Gel) and BaG nanoparticles in the ternary SiO 2-CaO-P 2O 5 system were prepared. In vitro evaluations of the nanocomposite scaffolds were performed, and for investigating their bioactive capacity these scaffolds were soaked in a simulated body fluid (SBF) at different time intervals. The scaffolds showed significant enhancement in bioactivity within few days of immersion in SBF solution. The apatite formation at the surface of the nanocomposite samples confirmed by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX) and X-ray powder diffraction (XRD) analyses. In vitro experiments with osteoblast cells indicated an appropriate penetration of the cells into the scaffold's pores, and also the continuous increase in cell aggregation on the bioactive scaffolds with increase in the incubation time demonstrated the ability of the scaffolds to support cell growth. The SEM observations revealed that the prepared scaffolds were porous with three dimensional (3D) and interconnected microstructure, pore size was 200-500 μm and the porosity was 72-86%. The nanocomposite scaffold made from Gel and BaG nanoparticles could be considered as a highly bioactive and potential bone tissue engineering implant.

  19. In vivo biocompatibility of custom-fabricated apatite-wollastonite-mesenchymal stromal cell constructs.

    PubMed

    Lee, Jennifer A; Knight, Charlotte A; Kun, Xiao; Yang, Xuebin B; Wood, David J; Dalgarno, Kenneth W; Genever, Paul G

    2015-10-01

    We have used the additive manufacturing technology of selective laser sintering (SLS), together with post SLS heat treatment, to produce porous three dimensional scaffolds from the glass-ceramic apatite-wollastonite (A-W). The A-W scaffolds were custom-designed to incorporate a cylindrical central channel to increase cell penetration and medium flow to the center of the scaffolds under dynamic culture conditions during in vitro testing and subsequent in vivo implantation. The scaffolds were seeded with human bone marrow mesenchymal stromal cells (MSCs) and cultured in spinner flasks. Using confocal and scanning electron microscopy, we demonstrated that MSCs formed and maintained a confluent layer of viable cells on all surfaces of the A-W scaffolds during dynamic culture. MSC-seeded, with and without osteogenic pre-differentiation, and unseeded A-W scaffolds were implanted subcutaneously in MF1 nude mice where osteoid formation and tissue in-growth were observed following histological assessment. The results demonstrate that the in vivo biocompatibility and osteo-supportive capacity of A-W scaffolds can be enhanced by SLS-custom design, without the requirement for osteogenic pre-induction, to advance their potential as patient-specific bone replacement materials. PMID:25777813

  20. Intense turquoise colors of apatite-type compounds with Mn5+ in tetrahedral coordination

    NASA Astrophysics Data System (ADS)

    Medina, Elena A.; Li, Jun; Stalick, Judith K.; Subramanian, M. A.

    2016-02-01

    The solid solutions of chlorapatite compounds Ba5Mn3-xVxO12Cl (x = 0-3.0) and Ba5Mn3-xPxO12Cl (x = 0-3.0) have been synthesized through solid state reactions and Pechini or sol-gel method using citric acid. The colors of the samples change from white (x = 3.0) through turquoise (x = 1.5) to dark green (x = 0) with increasing amount of manganese. Optical measurements reveal that the origin of the color is presumably a combination of d-d transitions of Mn5+ and cation-anion charge transfer from transition metals to oxygens. Near IR reflectance measurements indicate that synthesized compounds are promising materials for "cool pigments" applications. Magnetic measurements verify that manganese has two unpaired electrons and exhibits 5 + oxidation state. The IR spectra change systematically with sample compositions and the fingerprint region (700 cm-1 to 1100 cm-1) indicates characteristic bands belonging to (MnO4)3-, (VO4)3- and (PO4)3- functional groups. Structure refinements using neutron data confirm that Mn5+, V5+ and P5+ cations occupy the tetrahedral sites in the apatite structure.

  1. Insight into Bone-Derived Biological Apatite: Ultrastructure and Effect of Thermal Treatment

    PubMed Central

    Liu, Quan; Pan, Haobo; Chen, Zhuofan; Matinlinna, Jukka Pekka

    2015-01-01

    Objectives. This study aims at examining the ultrastructure of bone-derived biological apatite (BAp) from a series of small vertebrates and the effect of thermal treatment on its physiochemical properties. Materials and Methods. Femurs/fin rays and vertebral bodies of 5 kinds of small vertebrates were firstly analyzed with X-ray microtomography. Subsequently, BAp was obtained with thermal treatment and low power plasma ashing, respectively. The properties of BAp, including morphology, functional groups, and crystal characteristics were then analyzed. Results. The bones of grouper and hairtail were mainly composed of condensed bone. Spongy bone showed different distribution in the bones from frog, rat, and pigeon. No significant difference was found in bone mineral density of condensed bone and trabecular thickness of spongy bone. Only platelet-like crystals were observed for BAp obtained by plasma ashing, while rod-like and irregular crystals were both harvested from the bones treated by sintering. A much higher degree of crystallinity and larger crystal size but a lower content of carbonate were detected in the latter. Conclusion. Platelet-like BAp is the common inorganic component of vertebrate bones. BAp distributing in condensed and spongy bone may exhibit differing thermal reactivity. Thermal treatment may alter BAp's in vivo structure and composition. PMID:25695088

  2. Bioactive glasses with improved processing. Part 1. Thermal properties, ion release and apatite formation.

    PubMed

    Groh, Daniel; Döhler, Franziska; Brauer, Delia S

    2014-10-01

    Bioactive glasses, particularly Bioglass® 45S5, have been used to clinically regenerate human bone since the mid-1980s; however, they show a strong tendency to undergo crystallization upon heat treatment, which limits their range of applications. Attempts at improving their processing (by reducing their tendency to crystallize) have included increasing their silica content (and thus their network connectivity), incorporating intermediate oxides or reducing their phosphate content, all of which reduce glass bioactivity. Therefore, bioactive glasses known for their good processing (e.g. 13-93) are considerably less bioactive. Here, we investigated if the processing of 45S5 bioactive glass can be improved while maintaining its network connectivity and phosphate content. The results show that, by increasing the calcium:alkali cation ratio, partially substituting potassium for sodium (thereby making use of the mixed alkali effect) and adding small amounts of fluoride, bioactive glasses can be obtained which have a larger processing window (suggesting that they can be processed more easily, allowing for sintering of scaffolds or drawing into fibres) while degrading readily and forming apatite in aqueous solution within a few hours. PMID:24880003

  3. Improved interaction of osteoblast-like cells with apatite-nanodiamond coatings depends on fibronectin.

    PubMed

    Hristova, K; Pecheva, E; Pramatarova, L; Altankov, G

    2011-08-01

    New apatite (AP)/nanodiamond (ND) coating has been developed to improve physical and biological properties of stainless steel (SS) versus single AP coating. Homogeneously electrodeposited AP-ND layer demonstrates increased mechanical strength, interlayer cohesion and ductility. In the absence of serum, osteoblast-like MG63 cells attach well but poorly spread on both AP and AP-ND substrata. Pre-adsorption with serum or fibronectin (FN) improves the cellular interaction-an effect that is better pronounced on the AP-ND coating. In single protein adsorption study fluorescein isothiocyanate-labeled FN (FITC-FN) shows enhanced deposition on the AP-ND layer consistent with the significantly improved cell adhesion, spreading and focal adhesions formation (in comparison to SS and AP), particularly at low FN adsorption concentrations (1 μg/ml). Higher FN concentrations (20 μg/ml) abolish this difference suggesting that the promoted cellular interaction of serum (where FN is low) is caused by the greater affinity for FN. Moreover, it is found that MG63 cells tend to rearrange both adsorbed and secreted FN on the AP-ND layer suggesting facilitated FN matrix formation. PMID:21706219

  4. Tectonic significance of precambrian apatite fission-track ages from the midcontinent United States

    USGS Publications Warehouse

    Crowley, K.D.; Naeser, C.W.; Babel, C.A.

    1986-01-01

    Apparent apatite fission-track ages from drill core penetrating basement on the flank of the Transcontinental Arch in northwestern Iowa range from 934 ?? 86 to 641 ?? 90 Ma. These ages, the oldest reported in North America, record at least two thermal events. The 934 Ma age, which is synchronous with KAr ages in the Grenville Province and many KAr whole-rock and RbSr isochron ages from the Lake Superior region, may document basement cooling caused by regional uplift and erosion of the crust. The remaining fission-track ages are products of a more recent thermal event, relative to the age of the samples, which raised temperatures into the zone of partial annealing. Heating may have occurred between the Middle Ordovician and Middle Cretaceous by burial of the basement with additional sediment. It is estimated that burial raised temperatures in the part of the basement sampled by the core to between 50 and 75??C. These temperature estimates imply paleogeothermal gradients of about 20??C/km, approximately two and one-half times present-day values, and burial of the basement by an additional 2-3 km of sediment. ?? 198