Science.gov

Sample records for geological reference materials

  1. Evaluation of New Geological Reference Materials for U-Series Measurements

    NASA Astrophysics Data System (ADS)

    Denton, J. S.; Goldstein, S. J.; Nunn, A. J.; Ui Chearnaigh, K.; Amato, R.; Murrell, M. T.

    2012-12-01

    Uranium-series analytical measurements are widely used in geochemistry, geochronology, paleoclimatology, volcanology, environmental risk assessment and other fields. Recent advances in high-resolution, rapid, in situ microanalytical techniques e.g. LA-ICP-MS and SIMS present numerous opportunities for the geoanalytical community. As with other analytical techniques, the quality of the elemental concentration and isotopic data obtained through microanalytical techniques is dependent on the accurate characterization of suitable reference materials. Even for the case of fs-laser ablation applications, a range of well-characterized standards are required for high precision U-series work. Advances have been made in evaluating existing standard reference materials for U-series isotopic analysis, but this work is ongoing as more reference materials become available. In this study we present MC-TIMS and MC-ICP-MS results for uranium and thorium isotopic ratios and elemental concentrations measured in a suite of newly available Chinese Geological Standard Glasses (CGSG) designed for microanalysis. These glasses exhibit a range of chemical compositions including basalt, syenite, andesite and a soil. U concentrations for these glasses range from ≈2 to 14 μg/g and [Th]/[U] ratios range from ≈4 to 6. Uranium and thorium concentration and isotopic data will also be presented for rhyolitic obsidian from Macusani, SE Peru, which can be used as a rhyolitic reference material. These high-precision and high-accuracy ratios, from a suite of standards that exhibit a range of natural, non-basaltic compositions, will complement data from existing standards and expand the catalogue of reference materials that are appropriate for in situ U-series work. These results can be used to assess the performance of microanalytical techniques and will facilitate inter-laboratory comparison of data within the broader geoscience community.

  2. Evaluation of new geological reference materials for uranium-series measurements: Chinese Geological Standard Glasses (CGSG) and macusanite obsidian.

    PubMed

    Denton, J S; Murrell, M T; Goldstein, S J; Nunn, A J; Amato, R S; Hinrichs, K A

    2013-10-15

    Recent advances in high-resolution, rapid, in situ microanalytical techniques present numerous opportunities for the analytical community, provided accurately characterized reference materials are available. Here, we present multicollector thermal ionization mass spectrometry (MC-TIMS) and multicollector inductively coupled plasma mass spectrometry (MC-ICP-MS) uranium and thorium concentration and isotopic data obtained by isotope dilution for a suite of newly available Chinese Geological Standard Glasses (CGSG) designed for microanalysis. These glasses exhibit a range of compositions including basalt, syenite, andesite, and a soil. Uranium concentrations for these glasses range from ∼2 to 14 μg g(-1), Th/U weight ratios range from ∼4 to 6, (234)U/(238)U activity ratios range from 0.93 to 1.02, and (230)Th/(238)U activity ratios range from 0.98 to 1.12. Uranium and thorium concentration and isotopic data are also presented for a rhyolitic obsidian from Macusani, SE Peru (macusanite). This glass can also be used as a rhyolitic reference material, has a very low Th/U weight ratio (around 0.077), and is approximately in (238)U-(234)U-(230)Th secular equilibrium. The U-Th concentration data agree with but are significantly more precise than those previously measured. U-Th concentration and isotopic data agree within estimated errors for the two measurement techniques, providing validation of the two methods. The large (238)U-(234)U-(230)Th disequilibria for some of the glasses, along with the wide range in their chemical compositions and Th/U ratios should provide useful reference points for the U-series analytical community. PMID:24004454

  3. Evaluation of new geological reference materials for uranium-series measurements: Chinese Geological Standard Glasses (CGSG) and macusanite obsidian.

    PubMed

    Denton, J S; Murrell, M T; Goldstein, S J; Nunn, A J; Amato, R S; Hinrichs, K A

    2013-10-15

    Recent advances in high-resolution, rapid, in situ microanalytical techniques present numerous opportunities for the analytical community, provided accurately characterized reference materials are available. Here, we present multicollector thermal ionization mass spectrometry (MC-TIMS) and multicollector inductively coupled plasma mass spectrometry (MC-ICP-MS) uranium and thorium concentration and isotopic data obtained by isotope dilution for a suite of newly available Chinese Geological Standard Glasses (CGSG) designed for microanalysis. These glasses exhibit a range of compositions including basalt, syenite, andesite, and a soil. Uranium concentrations for these glasses range from ∼2 to 14 μg g(-1), Th/U weight ratios range from ∼4 to 6, (234)U/(238)U activity ratios range from 0.93 to 1.02, and (230)Th/(238)U activity ratios range from 0.98 to 1.12. Uranium and thorium concentration and isotopic data are also presented for a rhyolitic obsidian from Macusani, SE Peru (macusanite). This glass can also be used as a rhyolitic reference material, has a very low Th/U weight ratio (around 0.077), and is approximately in (238)U-(234)U-(230)Th secular equilibrium. The U-Th concentration data agree with but are significantly more precise than those previously measured. U-Th concentration and isotopic data agree within estimated errors for the two measurement techniques, providing validation of the two methods. The large (238)U-(234)U-(230)Th disequilibria for some of the glasses, along with the wide range in their chemical compositions and Th/U ratios should provide useful reference points for the U-series analytical community.

  4. Platinum stable isotope analysis of geological standard reference materials by double-spike MC-ICPMS

    PubMed Central

    Creech, J.B.; Baker, J.A.; Handler, M.R.; Bizzarro, M.

    2015-01-01

    We report a method for the chemical purification of Pt from geological materials by ion-exchange chromatography for subsequent Pt stable isotope analysis by multiple-collector inductively coupled plasma mass spectrometry (MC-ICPMS) using a 196Pt-198Pt double-spike to correct for instrumental mass bias. Double-spiking of samples was carried out prior to digestion and chemical separation to correct for any mass-dependent fractionation that may occur due to incomplete recovery of Pt. Samples were digested using a NiS fire assay method, which pre-concentrates Pt into a metallic bead that is readily dissolved in acid in preparation for anion-exchange chemistry. Pt was recovered from anion-exchange resin in concentrated HNO3 acid after elution of matrix elements, including the other platinum group elements (PGE), in dilute HCl and HNO3 acids. The separation method has been calibrated using a precious metal standard solution doped with a range of synthetic matrices and results in Pt yields of ≥90% with purity of ≥95%. Using this chemical separation technique, we have separated Pt from 11 international geological standard reference materials comprising of PGE ores, mantle rocks, igneous rocks and one sample from the Cretaceous–Paleogene boundary layer. Pt concentrations in these samples range from ca. 5 ng g−1 to 4 μg g−1. This analytical method has been shown to have an external reproducibility on δ198Pt (permil difference in the 198Pt/194Pt ratio from the IRMM-010 standard) of ±0.040 (2 sd) on Pt solution standards (Creech et al., 2013, J. Anal. At. Spectrom. 28, 853-865). The reproducibility in natural samples is evaluated by processing multiple replicates of four standard reference materials, and is conservatively taken to be ca. ±0.088 (2 sd). Pt stable isotope data for the full set of reference materials have a range of δ198Pt values with offsets of up to 0.4‰ from the IRMM-010 standard, which are readily resolved with this technique. These results

  5. Hf isotope compositions of U.S. Geological Survey reference materials

    NASA Astrophysics Data System (ADS)

    Weis, Dominique; Kieffer, Bruno; Hanano, Diane; Nobre Silva, Inês; Barling, Jane; Pretorius, Wilma; Maerschalk, Claude; Mattielli, Nadine

    2007-06-01

    A systematic multi-isotopic and trace element characterization of U.S. Geological Survey reference materials has been carried out at the Pacific Centre for Isotopic and Geochemical Research, University of British Columbia. Values of 176Hf/177Hf are recommended for the following reference materials (mean ±2 SD): G-2: 0.282523 ± 6; G-3: 0.282518 ± 1; GSP-2: 0.281949 ± 8; RGM-1: 0.283017 ± 13; STM-1: 0.283019 ± 12; STM-2: 0.283021 ± 5; BCR-1: 0.282875 ± 8; BCR-2: 0.282870 ± 8; BHVO-1: 0.283106 ± 12; BHVO-2: 0.283105 ± 11; AGV-1: 0.282979 ± 6; and AGV-2: 0.282984 ± 9. Reproducibility is better than 50 ppm for the granitoid compositions and better than 40 ppm for the basaltic/andesitic compositions. For the isotopic analyses acquired early in this project on glass columns, Hf isotopic analyses from several of the reference materials were significantly less reproducible than Nd and Sr isotopic analyses determined from the same sample dissolution. The 176Hf/177Hf ratios for relatively radiogenic compositions (BCR-1, 2; BHVO-1, 2; RGM-1) were shifted systematically toward lower values by 100-150 ppm when a borosilicate primary column was used. Although systematic, the shift for felsic compositions was generally within analytical error, except for GSP-2, which has a very low Hf isotopic ratio, where the shift was to higher 176Hf/177Hf. Trace element and isotopic characterization of the borosilicate glass column, borosilicate frits, and quartz columns reveals extremely variable levels of trace elements. The 176Hf/177Hf ratios for these materials are very unradiogenic (borosilicate glass <0.28220 frit = 0.28193 ± 4). The borosilicate frit material appears to be the most variable in elemental concentration and isotopic composition. The quartz material has very low levels (material (22 ppm) indicate that only small amounts of such unradiogenic

  6. Earth's earliest biosphere-a proposal to develop a collection of curated archean geologic reference materials.

    PubMed

    Lindsay, John F; McKay, David S; Allen, Carlton C

    2003-01-01

    The discovery of evidence indicative of life in a Martian meteorite has led to an increase in interest in astrobiology. As a result of this discovery, and the ensuing controversy, it has become apparent that our knowledge of the early development of life on Earth is limited. Archean stratigraphic successions containing evidence of Earth's early biosphere are well preserved in the Pilbara Craton of Western Australia. The craton includes part of a protocontinent consisting of granitoid complexes that were emplaced into, and overlain by, a 3.51-2.94 Ga volcanigenic carapace - the Pilbara Supergroup. The craton is overlain by younger supracrustal basins that form a time series recording Earth history from approximately 2.8 Ga to approximately 1.9 Ga. It is proposed that a well-documented suite of these ancient rocks be collected as reference material for Archean and astrobiological research. All samples would be collected in a well-defined geological context in order to build a framework to test models for the early evolution of life on Earth and to develop protocols for the search for life on other planets.

  7. Earth's earliest biosphere-a proposal to develop a collection of curated archean geologic reference materials

    NASA Technical Reports Server (NTRS)

    Lindsay, John F.; McKay, David S.; Allen, Carlton C.

    2003-01-01

    The discovery of evidence indicative of life in a Martian meteorite has led to an increase in interest in astrobiology. As a result of this discovery, and the ensuing controversy, it has become apparent that our knowledge of the early development of life on Earth is limited. Archean stratigraphic successions containing evidence of Earth's early biosphere are well preserved in the Pilbara Craton of Western Australia. The craton includes part of a protocontinent consisting of granitoid complexes that were emplaced into, and overlain by, a 3.51-2.94 Ga volcanigenic carapace - the Pilbara Supergroup. The craton is overlain by younger supracrustal basins that form a time series recording Earth history from approximately 2.8 Ga to approximately 1.9 Ga. It is proposed that a well-documented suite of these ancient rocks be collected as reference material for Archean and astrobiological research. All samples would be collected in a well-defined geological context in order to build a framework to test models for the early evolution of life on Earth and to develop protocols for the search for life on other planets.

  8. Earth's earliest biosphere-a proposal to develop a collection of curated archean geologic reference materials.

    PubMed

    Lindsay, John F; McKay, David S; Allen, Carlton C

    2003-01-01

    The discovery of evidence indicative of life in a Martian meteorite has led to an increase in interest in astrobiology. As a result of this discovery, and the ensuing controversy, it has become apparent that our knowledge of the early development of life on Earth is limited. Archean stratigraphic successions containing evidence of Earth's early biosphere are well preserved in the Pilbara Craton of Western Australia. The craton includes part of a protocontinent consisting of granitoid complexes that were emplaced into, and overlain by, a 3.51-2.94 Ga volcanigenic carapace - the Pilbara Supergroup. The craton is overlain by younger supracrustal basins that form a time series recording Earth history from approximately 2.8 Ga to approximately 1.9 Ga. It is proposed that a well-documented suite of these ancient rocks be collected as reference material for Archean and astrobiological research. All samples would be collected in a well-defined geological context in order to build a framework to test models for the early evolution of life on Earth and to develop protocols for the search for life on other planets. PMID:14987479

  9. Neutron-activation analysis of several US Geological Survey and National Bureau of Standards reference materials

    SciTech Connect

    Daly, A.T.

    1981-01-01

    In this work, several US Geological Survey (U.S.G.S.) and National Bureau of Standards (N.B.S.) reference samples have been analyzed in an effort to improve the quality of elemental concentration data available on these materials, so they can be used in a program of verification of factor analysis source resolution procedures. The analyses of these samples were performed by instrumental neutron activation analysis (INAA). The samples analyzed were: U.S.G.S. Green River Shale, N.B.S. 45b Homogeneous River Sediment, U.S.G.S. Analyzed Peridotite N.B.S. 1579 Powdered Lead-based Paint, U.S.G.S. Hawaian Basalt U.S.G.S. Marine Mud, U.S.G.S. Analyzed Cody Shale U.S.G.S. Glass Mountain Rhyolite, N.B.S. Argillaceous Limestone No. 1, and a sample of Spex ultrapure graphite. Neutron activation analysis was employed because of the high sensitivity that can be attained in determining elemental concentrations. Although INAA is a relatively simple method and the reproducibility of the data is good, the method shows some inaccuracies. The basic theory and technique are reviewed in an attempt to show where problems can arise and how they can be dealt with.

  10. Reference Materials

    NASA Astrophysics Data System (ADS)

    Merkus, Henk G.

    Reference materials for measurement of particle size and porosity may be used for calibration or qualification of instruments or for validation of operating procedures or operators. They cover a broad range of materials. On the one hand there are the certified reference materials, for which governmental institutes have certified one or more typical size or porosity values. Then, there is a large group of reference materials from commercial companies. And on the other hand there are typical products in a given line of industry, where size or porosity values come from the analysis laboratory itself or from some round-robin test in a group of industrial laboratories. Their regular application is essential for adequate quality control of particle size and porosity measurement, as required in e.g., ISO 17025 on quality management. In relation to this, some quality requirements for certification are presented.

  11. Determination of elements in National Bureau of Standards' geological Standard Reference Materials by neutron activation analysis

    SciTech Connect

    Graham, C.C.; Glascock, M.D.; Carni, J.J.; Vogt, J.R.; Spalding, T.G.

    1982-08-01

    Instrumental neutron activation analysis (INAA) and prompt gamma neutron activation analysis (PGNAA) have been used to determine elemental concentrations in two recently issued National Bureau of Standards (NBS) Standard Reference Materials (SRM's). The results obtained are in good agreement with the certified and information values reported by NBS for those elements in each material for which comparisons are available. Average concentrations of 35 elements in SRM 278 obsidian rock and 32 elements in SRM 688 basalt rock are reported for comparison with results that may be obtained by other laboratories.

  12. Choosing optimal exposure times for XRF core-scanning: Suggestions based on the analysis of geological reference materials

    NASA Astrophysics Data System (ADS)

    Huang, Jyh-Jaan; Löwemark, Ludvig; Chang, Queenie; Lin, Tzu-Yu; Chen, Huei-Fen; Song, Sheng-Rong; Wei, Kuo-Yen

    2016-04-01

    X-ray fluorescence (XRF) core-scanning is a fast and nondestructive technique to assess elemental variations of unprocessed sediments. However, although the exposure time of XRF-scanning directly affects the scanning counts and total measurement time, only a few studies have considered the influence of exposure time during the scan. How to select an optimal exposure time to achieve reliable results and reduce the total measurement time is an important issue. To address this question, six geological reference materials from the Geological Survey of Japan (JLK-1, JMS-1, JMS-2, JSD-1, JSD-2, and JSD-3) were scanned by the Itrax-XRF core scanner using the Mo- and the Cr-tube with different exposure times to allow a comparison of scanning counts with absolute concentrations. The regression lines and correlation coefficients of elements that are generally used in paleoenvironmental studies were examined for the different exposure times and X-ray tubes. The results show that for those elements with relatively high concentrations or high detectability, the correlation coefficients are higher than 0.90 for all exposure times. In contrast, for the low detectability or low concentration elements, the correlation coefficients are relatively low, and improve little with increased exposure time. Therefore, we suggest that the influence of different exposure times is insignificant for the accuracy of the measurements. Thus, caution must be taken when interpreting the results of elements with low detectability, even when the exposure times are long and scanning counts are reasonably high.

  13. [Determination of Sb and Bi in 24 international geological reference materials by using pressurized acid digestion-ICP-MS].

    PubMed

    Hu, Zhao-chu; Gao, Shan; Liu, Xiao-ming; Yuan, Hong-lin; Liu, Ye; Diwu, Chun-rong

    2007-12-01

    The authors studied in detail the memory effect of Bi, Sb, As and Te in ICP-MS. The produced memory effects of these element were in the order of Bi>Sb>Te>As. Bi was seriously adsorbed by the polypropylene sample storing bottle and the sample introduction system in the low nitric acid medium (0.01%-1% HNO3). The washout effect of 0.1% HF was found to be better than those of 6% HNO3 and 0.1% HClO4. Under the given experiment conditions, the instrumental limit of detection was 0.001 and 0.0001 ng x mL(-1) for Sb and Bi, respectively. The authors report the determination of Sb and Bi in 24 international geological reference materials by using pressurized acid digestion-ICP-MS (including AGV-2, BHVO-2, BCR-2, etc.). Most of the results were found to be in reasonable agreement with the reported values in the literature. The authors' determined values of Sb for GSR-1 (granite; 0.30 microg x g(-1)) and JP-1 (peridotite; 0.045 microg x g(-1)) are obviously higher than those reported values. This is attributed to the efficient pressurized acid digestion, which is generally much more efficient than conventional wet digestions for insoluble minerals. PMID:18330312

  14. [Determination of Sb and Bi in 24 international geological reference materials by using pressurized acid digestion-ICP-MS].

    PubMed

    Hu, Zhao-chu; Gao, Shan; Liu, Xiao-ming; Yuan, Hong-lin; Liu, Ye; Diwu, Chun-rong

    2007-12-01

    The authors studied in detail the memory effect of Bi, Sb, As and Te in ICP-MS. The produced memory effects of these element were in the order of Bi>Sb>Te>As. Bi was seriously adsorbed by the polypropylene sample storing bottle and the sample introduction system in the low nitric acid medium (0.01%-1% HNO3). The washout effect of 0.1% HF was found to be better than those of 6% HNO3 and 0.1% HClO4. Under the given experiment conditions, the instrumental limit of detection was 0.001 and 0.0001 ng x mL(-1) for Sb and Bi, respectively. The authors report the determination of Sb and Bi in 24 international geological reference materials by using pressurized acid digestion-ICP-MS (including AGV-2, BHVO-2, BCR-2, etc.). Most of the results were found to be in reasonable agreement with the reported values in the literature. The authors' determined values of Sb for GSR-1 (granite; 0.30 microg x g(-1)) and JP-1 (peridotite; 0.045 microg x g(-1)) are obviously higher than those reported values. This is attributed to the efficient pressurized acid digestion, which is generally much more efficient than conventional wet digestions for insoluble minerals.

  15. Geological and Inorganic Materials.

    ERIC Educational Resources Information Center

    Jackson, L. L.; And Others

    1989-01-01

    Presents a review focusing on techniques and their application to the analysis of geological and inorganic materials that offer significant changes to research and routine work. Covers geostandards, spectroscopy, plasmas, microbeam techniques, synchrotron X-ray methods, nuclear activation methods, chromatography, and electroanalytical methods.…

  16. USGS reference materials

    USGS Publications Warehouse

    ,

    1995-01-01

    Every year in the United States, millions of measurements are made on the chemical composition of items that affect us on a daily basis. Determining the accuracy of these measurements is based on the analysis of appropriate reference materials whose composition was previously determined through rigorous testing. Today, reference materials help us evaluate the composition of the food we eat, medicine we use, soil we grow our crops in, and hundreds of other products that affect our everyday lives.

  17. Isotope reference materials

    USGS Publications Warehouse

    Coplen, Tyler B.

    2010-01-01

    Measurement of the same isotopically homogeneous sample by any laboratory worldwide should yield the same isotopic composition within analytical uncertainty. International distribution of light element isotopic reference materials by the International Atomic Energy Agency and the U.S. National Institute of Standards and Technology enable laboratories to achieve this goal.

  18. Reference Material for Seebeck Coefficients

    NASA Astrophysics Data System (ADS)

    Edler, F.; Lenz, E.; Haupt, S.

    2015-03-01

    This paper describes a measurement method and a measuring system to determine absolute Seebeck coefficients of thermoelectric bulk materials with the aim of establishing reference materials for Seebeck coefficients. Reference materials with known thermoelectric properties are essential to allow a reliable benchmarking of different thermoelectric materials for application in thermoelectric generators to convert thermal into electrical energy or vice versa. A temperature gradient (1 to 8) K is induced across the sample, and the resulting voltage is measured by using two differential Au/Pt thermocouples. On the basis of the known absolute Seebeck coefficients of Au and Pt, the unknown Seebeck coefficient of the sample is calculated. The measurements are performed in inert atmospheres and at low pressure (30 to 60) mbar in the temperature range between 300 K and 860 K. The measurement results of the Seebeck coefficients of metallic and semiconducting samples are presented. Achievable relative measurement uncertainties of the Seebeck coefficient are on the order of a few percent.

  19. Criminal Justice - Selected Reference Materials.

    ERIC Educational Resources Information Center

    McClure, John D., III, Comp.

    This bibliography reviews approximately 70 reference materials on criminal justice. Entries are presented in eight categories--dictionaries, indexes and abstracts, professional position papers, working conditions and unions, law and the police, crime, prisons and prisoners, and victimization. Types of publications included under the subject…

  20. Infrared Analysis of Geological Materials.

    ERIC Educational Resources Information Center

    Brown, Alan; Clark, E. Roy

    1980-01-01

    Describes the infrared analysis of geological specimens which can form the basis of a laboratory exercise, allowing some minerals to be identified by "fingerprint" technique. Students can gain insight into the concept of symmetry and environment around an atom. (Author/SA)

  1. Health benefits of geologic materials and geologic processes

    USGS Publications Warehouse

    Finkelman, R.B.

    2006-01-01

    The reemerging field of Medical Geology is concerned with the impacts of geologic materials and geologic processes on animal and human health. Most medical geology research has been focused on health problems caused by excess or deficiency of trace elements, exposure to ambient dust, and on other geologically related health problems or health problems for which geoscience tools, techniques, or databases could be applied. Little, if any, attention has been focused on the beneficial health effects of rocks, minerals, and geologic processes. These beneficial effects may have been recognized as long as two million years ago and include emotional, mental, and physical health benefits. Some of the earliest known medicines were derived from rocks and minerals. For thousands of years various clays have been used as an antidote for poisons. "Terra sigillata," still in use today, may have been the first patented medicine. Many trace elements, rocks, and minerals are used today in a wide variety of pharmaceuticals and health care products. There is also a segment of society that believes in the curative and preventative properties of crystals (talismans and amulets). Metals and trace elements are being used in some of today's most sophisticated medical applications. Other recent examples of beneficial effects of geologic materials and processes include epidemiological studies in Japan that have identified a wide range of health problems (such as muscle and joint pain, hemorrhoids, burns, gout, etc.) that may be treated by one or more of nine chemically distinct types of hot springs, and a study in China indicating that residential coal combustion may be mobilizing sufficient iodine to prevent iodine deficiency disease. ?? 2006 MDPI. All rights reserved.

  2. Health benefits of geologic materials and geologic processes.

    PubMed

    Finkelman, Robert B

    2006-12-01

    The reemerging field of Medical Geology is concerned with the impacts of geologic materials and geologic processes on animal and human health. Most medical geology research has been focused on health problems caused by excess or deficiency of trace elements, exposure to ambient dust, and on other geologically related health problems or health problems for which geoscience tools, techniques, or databases could be applied. Little, if any, attention has been focused on the beneficial health effects of rocks, minerals, and geologic processes. These beneficial effects may have been recognized as long as two million years ago and include emotional, mental, and physical health benefits. Some of the earliest known medicines were derived from rocks and minerals. For thousands of years various clays have been used as an antidote for poisons. "Terra sigillata," still in use today, may have been the first patented medicine. Many trace elements, rocks, and minerals are used today in a wide variety of pharmaceuticals and health care products. There is also a segment of society that believes in the curative and preventative properties of crystals (talismans and amulets). Metals and trace elements are being used in some of today's most sophisticated medical applications. Other recent examples of beneficial effects of geologic materials and processes include epidemiological studies in Japan that have identified a wide range of health problems (such as muscle and joint pain, hemorrhoids, burns, gout, etc.) that may be treated by one or more of nine chemically distinct types of hot springs, and a study in China indicating that residential coal combustion may be mobilizing sufficient iodine to prevent iodine deficiency disease. PMID:17159275

  3. High Precision Isotopic Reference Material Program

    NASA Astrophysics Data System (ADS)

    Mann, J. L.; Vocke, R. D.

    2007-12-01

    Recent developments in thermal ionization and inductively coupled plasma multicollector mass spectrometers have lead to "high precision" isotope ratio measurements with uncertainties approaching a few parts in 106. These new measurement capabilities have revolutionized the study of isotopic variations in nature by increasing the number of elements showing natural variations by almost a factor of two, and new research areas are actively opening up in climate change, health, ecology, geology and forensic studies. Because the isotopic applications are impacting very diverse fields, there is at present little effective coordination between research laboratories over reference materials and the values to apply to those materials. NIST had originally developed the techniques for producing accurate isotopic characterizations, culminating in the NIST Isotopic SRM series. The values on existing materials however are insufficiently precise and, in some cases, may be isotopically heterogeneous. A new generation of isotopic standards is urgently needed and will directly affect the quality and scope of emergent applications and ensure that the results being derived from these diverse fields are comparable. A series of new isotopic reference materials similar to the NIST 3100 single element solution series is being designed for this purpose and twelve elements have been selected as having the most pressing need. In conjunction with other expert users and National Metrology Institutes, an isotopic characterization of the respective 12 selected ampoules from the NIST single element solution series is currently underway. In this presentation the preliminary results of this screening will be discussed as well as the suitability of these materials in terms of homogeneity and purity, long term stability and availability, and isotopic relevance. Approaches to value assignment will also be discussed.

  4. 40 CFR 1042.910 - Reference materials.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone may inspect copies at the U.S. EPA, Air... 40 Protection of Environment 34 2012-07-01 2012-07-01 false Reference materials. 1042.910 Section... Other Reference Information § 1042.910 Reference materials. Documents listed in this section have...

  5. 40 CFR 1042.910 - Reference materials.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone may inspect copies at the U.S. EPA, Air... 40 Protection of Environment 33 2011-07-01 2011-07-01 false Reference materials. 1042.910 Section... Other Reference Information § 1042.910 Reference materials. Documents listed in this section have...

  6. Impact jetting of geological materials.

    NASA Astrophysics Data System (ADS)

    Yang, Wenbo; Ahrens, Thomas J.

    1995-08-01

    To understand jetting of earth materials, gabbro slabs (5 mm thick) were accelerated to 1.5-2 km sec -1 and impacted gabbro (5-10 mm thick), novaculite (10 mm thick), and porous sandstone (12 mm thick) targets at inclination angles of 30°-60°. The ejecta were collected using a catcher box filled with styrofoam and the particles are extracted using chloroform. Jetting angles are determined by the relative positions of the target and the crater produced by the ejecta. The mass of the ejected particles per unit area (˜50 mg cm -2) of the impactor remains almost independent of the impact velocity, inclination angle, thickness of the target and sample mineralogy, and density. Hydrodynamic models are used to calculate the jetting mass, angle, and velocity. Theoretical models predict ˜6 times more ejecta than the experimentally measured as the inclination angle increases. X-ray diffraction of the recovered ejecta shows that it is still in crystalline form, which agrees with thermodynamic calculations. Because the experimental results indicate that the theoretical jetting model for thin metal plates provides a poor description of the experiments, the application of metal plate theory to planet-sized objects appears to be questionable.

  7. Reference materials for cellular therapeutics.

    PubMed

    Bravery, Christopher A; French, Anna

    2014-09-01

    The development of cellular therapeutics (CTP) takes place over many years, and, where successful, the developer will anticipate the product to be in clinical use for decades. Successful demonstration of manufacturing and quality consistency is dependent on the use of complex analytical methods; thus, the risk of process and method drift over time is high. The use of reference materials (RM) is an established scientific principle and as such also a regulatory requirement. The various uses of RM in the context of CTP manufacturing and quality are discussed, along with why they are needed for living cell products and the analytical methods applied to them. Relatively few consensus RM exist that are suitable for even common methods used by CTP developers, such as flow cytometry. Others have also identified this need and made proposals; however, great care will be needed to ensure any consensus RM that result are fit for purpose. Such consensus RM probably will need to be applied to specific standardized methods, and the idea that a single RM can have wide applicability is challenged. Written standards, including standardized methods, together with appropriate measurement RM are probably the most appropriate way to define specific starting cell types. The characteristics of a specific CTP will to some degree deviate from those of the starting cells; consequently, a product RM remains the best solution where feasible. Each CTP developer must consider how and what types of RM should be used to ensure the reliability of their own analytical measurements.

  8. Flameless atomic-absorption determination of gold in geological materials

    USGS Publications Warehouse

    Meier, A.L.

    1980-01-01

    Gold in geologic material is dissolved using a solution of hydrobromic acid and bromine, extracted with methyl isobutyl ketone, and determined using an atomic-absorption spectrophotometer equipped with a graphite furnace atomizer. A comparison of results obtained by this flameless atomic-absorption method on U.S. Geological Survey reference rocks and geochemical samples with reported values and with results obtained by flame atomic-absorption shows that reasonable accuracy is achieved with improved precision. The sensitivity, accuracy, and precision of the method allows acquisition of data on the distribution of gold at or below its crustal abundance. ?? 1980.

  9. 49 CFR 171.7 - Reference material.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... Director of the Federal Register in accordance with 5 U.S.C 552(a) and 1 CFR part 51. Material is... information only and may not be all inclusive. Source and name of material 49 CFR reference Air Transport... sections in which the material is referenced. Source and name of material 49 CFR reference...

  10. Reference materials for new psychoactive substances.

    PubMed

    Archer, Roland P; Treble, Ric; Williams, Keith

    2011-01-01

    Historically, the appearance of new psychoactive materials (and hence the requirement for new reference standards) has been relatively slow. This position has now changed, with 101 new psychoactive substances reported to EMCDDA-Europol since 2006. The newly reported materials, and associated metabolites, require properly certified reference materials to permit reliable identification and quantification. The traditional approach and timescales of reference material production and certification are being increasingly challenged by the appearance of these new substances. Reference material suppliers have to adopt new strategies to meet the needs of laboratories. This situation is particularly challenging for toxicology standards as the metabolism of many of these substances is initially unknown. Reference material production often involves synthesis from first principles. While it is possible to synthesis these materials, there can be significant difficulties, from synthetic complexities through to the need to use controlled materials. These issues are examined through a discussion of the synthesis of cathinones. Use of alternative sources, including pharmaceutical impurity materials or internet sourced products, as starting materials for conversion into appropriately certified reference materials are also discussed. The sudden appearance and sometimes brief lifetime in the market place of many of these novel legal highs or research chemicals present commercial difficulties for reference material producers. The need for collaboration at all levels is highlighted as essential to rapid identification of requirements for new reference materials. National or international commissioning or support may also be required to permit reference material producers to recover their development costs. PMID:21744516

  11. Bisphenol A polycarbonate as a reference material

    NASA Technical Reports Server (NTRS)

    Hilado, C. J.; Cumming, H. J.; Williams, J. B.

    1977-01-01

    Test methods require reference materials to standardize and maintain quality control. Various materials have been evaluated as possible reference materials, including a sample of bisphenol A polycarbonate without additives. Screening tests for relative toxicity under various experimental conditions were performed using male mice exposed to pyrolysis effluents over a 200-800 C temperature range. It was found that the bisphenol A polycarbonate served as a suitable reference material as it is available in large quantities, and does not significantly change with time.

  12. 49 CFR 171.7 - Reference material.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... incorporation by reference by the Director of the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR..., into § 173.417. (2) Table 1 to 49 CFR 171.7—Materials Not Incorporated by Reference Source and name of material 49 CFR reference American Biological Safety Association 1202 Allanson Road, Mundelein, IL...

  13. 49 CFR 171.7 - Reference material.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... incorporation by reference by the Director of the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR..., amendment 1 (2011). Table 1 to 49 CFR 171.7—Materials Not Incorporated by Reference Source and name of material 49 CFR reference American Biological Safety Association 1202 Allanson Road, Mundelein, IL...

  14. 40 CFR 1043.100 - Reference materials.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone may inspect copies at the U.S. EPA, Air and Radiation... 40 Protection of Environment 33 2011-07-01 2011-07-01 false Reference materials. 1043.100 Section... § 1043.100 Reference materials. Documents listed in this section have been incorporated by reference...

  15. 40 CFR 1043.100 - Reference materials.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone may inspect copies at the U.S. EPA, Air and Radiation... 40 Protection of Environment 34 2012-07-01 2012-07-01 false Reference materials. 1043.100 Section... § 1043.100 Reference materials. Documents listed in this section have been incorporated by reference...

  16. The need for new isotope reference materials.

    PubMed

    Vogl, Jochen; Rosner, Martin; Pritzkow, Wolfgang

    2013-03-01

    Isotope reference materials are needed to calibrate and validate analytical procedures used for the determination of isotope amount ratios, procedurally defined isotope ratios or so-called δ values. In contrast to the huge analytical progress in isotope ratio analytics, the production of isotope reference materials has not kept pace with the increasing needs of isotope analysts. Three representative isotope systems are used to explain the technical and non-technical difficulties and drawbacks, on one hand, and to demonstrate what can be achieved at its best, on the other hand. A clear statement is given that new isotope reference materials are needed to obtain traceable and thus comparable data, which is essential for all kinds of isotope research. The range of available isotope reference materials and δ reference materials should be increased and matrix reference materials certified for isotope compositions or δ values, which do not exist yet, should be provided.

  17. 40 CFR 1066.710 - Reference materials.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Practice for Measuring Fuel Economy and Emissions of Hybrid-Electric and Conventional Heavy-Duty Vehicles... VEHICLE-TESTING PROCEDURES Definitions and Other Reference Material § 1066.710 Reference materials. (a... Federal Register under 5 U.S.C. 552(a) and 1 CFR part 51. To enforce any edition other than that...

  18. A new basaltic glass microanalytical reference material for multiple techniques

    USGS Publications Warehouse

    Wilson, Steve; Koenig, Alan; Lowers, Heather

    2012-01-01

    The U.S. Geological Survey (USGS) has been producing reference materials since the 1950s. Over 50 materials have been developed to cover bulk rock, sediment, and soils for the geological community. These materials are used globally in geochemistry, environmental, and analytical laboratories that perform bulk chemistry and/or microanalysis for instrument calibration and quality assurance testing. To answer the growing demand for higher spatial resolution and sensitivity, there is a need to create a new generation of microanalytical reference materials suitable for a variety of techniques, such as scanning electron microscopy/X-ray spectrometry (SEM/EDS), electron probe microanalysis (EPMA), laser ablation inductively coupled mass spectrometry (LA-ICP-MS), and secondary ion mass spectrometry (SIMS). As such, the microanalytical reference material (MRM) needs to be stable under the beam, be homogeneous at scales of better than 10–25 micrometers for the major to ultra-trace element level, and contain all of the analytes (elements or isotopes) of interest. Previous development of basaltic glasses intended for LA-ICP-MS has resulted in a synthetic basaltic matrix series of glasses (USGS GS-series) and a natural basalt series of glasses (BCR-1G, BHVO-2G, and NKT-1G). These materials have been useful for the LA-ICP-MS community but were not originally intended for use by the electron or ion beam community. A material developed from start to finish with intended use in multiple microanalytical instruments would be useful for inter-laboratory and inter-instrument platform comparisons. This article summarizes the experiments undertaken to produce a basalt glass reference material suitable for distribution as a multiple-technique round robin material. The goal of the analytical work presented here is to demonstrate that the elemental homogeneity of the new glass is acceptable for its use as a reference material. Because the round robin exercise is still underway, only

  19. Performance criteria for reference measurement procedures and reference materials.

    PubMed

    Schimmel, Heinz; Zegers, Ingrid

    2015-05-01

    The concept of metrological traceability of measurement results to property values assigned to measurement standards of higher metrological order or to the International System of Units (SI) through sequential calibrations, using reference materials and reference measurement procedures, plays a key role in ensuring that end user measurement procedures perform at an acceptable level in the clinical context. The aim is that measurement results produced over time or by different end users or with different end user measurement procedures for the same measurand will be equivalent within their corresponding uncertainties. These goals can only be reached under certain conditions and if requirements laid down in international standards on calibration concepts, reference measurement procedures and reference materials are fulfilled. Calibration hierarchies have to be implemented correctly and parameters contributing to measurement uncertainty and systematic bias need to be controlled and eliminated, respectively, by technically improving methods and reference materials and intermediate calibrators used for effectively achieving equivalence of measurement results and for meeting analytical performance requirements for in vitro diagnostic devices.

  20. Overview of Uranium Isotopic Reference Materials at IRMM

    NASA Astrophysics Data System (ADS)

    Alonso-Munoz, A.; Richter, S.; Eykens, R.; Aregbe, Y.; Kuehn, H.; Verbruggen, A.

    2007-12-01

    For many applications in the geological sciences, in particular in geochemistry research, isotope ratio measurements play a significant role. For instance, in geochronology isotope abundances of uranium and its daughter products thorium and lead have been used since more than five decades to determine the age of various samples of geological interest. However, in order to validate mass spectrometric measurement procedures and to calibrate detector systems, suitable isotope reference materials are needed. IRMM is a well recognized provider for nuclear isotope reference materials to the nuclear industry and nuclear safeguards authorities, which can also be used for geological applications. This paper gives an overview of isotope reference materials for uranium prepared and certified at IRMM. These materials are synthetic isotope reference materials prepared based on proven methods of purifying and mixing highly enriched oxides. Firstly, a set of 10 mixtures of 233U, 235U and 238U was made in which the 235U/238U ratios were kept at 1:1 and the 233U/235U ratios varied from 1.0 to 10-6 (IRMM-072). This set is ideal for checking the linearity response of detectors used in isotope mass spectrometry. Recently, after the IRMM-072 series was exhausted, it has been replaced by the IRMM-073 and IRMM-074 series. Secondly the double spike IRMM-3636 with a 233U/236U ratio of 1:1 was prepared which allows internal mass fractionation correction for high precision 235U/238U ratio measurements. The 234U abundance of this double spike material is low enough to allow an accurate and precise correction of 234U/238U ratios, even for measurements of close to equilibrium uranium samples.

  1. 40 CFR 94.5 - Reference materials.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone may inspect copies at the U.S. EPA, Air...: Table 2 of § 94.5—ISO Materials Document No. and name 40 CFR part 94 reference ISO 8178-1, Reciprocating... name 40 CFR part 94 reference Resolution 2—Technical Code on Control of Emission of Nitrogen...

  2. 40 CFR 94.5 - Reference materials.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone may inspect copies at the U.S. EPA, Air...: Table 2 of § 94.5—ISO Materials Document No. and name 40 CFR part 94 reference ISO 8178-1, Reciprocating... name 40 CFR part 94 reference Resolution 2—Technical Code on Control of Emission of Nitrogen...

  3. 49 CFR 171.7 - Reference material.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... Director of the Federal Register in accordance with 5 U.S.C 552(a) and 1 CFR part 51. Material is... information only and may not be all inclusive. Source and name of material 49 CFR reference Air Transport... for Pipe, Steel, Black and Hot-Dipped, Zinc-Coated, Welded and Seamless 173.5b. ASTM A 106, ASTM A...

  4. 49 CFR 171.7 - Reference material.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... Director of the Federal Register in accordance with 5 U.S.C 552(a) and 1 CFR part 51. Material is... information only and may not be all inclusive. Source and name of material 49 CFR reference Air Transport... for Pipe, Steel, Black and Hot-Dipped, Zinc-Coated, Welded and Seamless 173.5b. ASTM A 106, ASTM A...

  5. Reading Materials in Large Type. Reference Circular.

    ERIC Educational Resources Information Center

    Ovenshire, Ruthann, Comp.

    Listed in the circular are approximately 32 commercial and volunteer producers of large type materials, approximately 50 large type books for reference and special needs, and five further sources of large type materials. Usually given for each alphabetically listed producer are the address, specialty (whether producer of specific categories or of…

  6. Polyfluorinated substances in abiotic standard reference materials

    EPA Science Inventory

    The National Institute of Standards and Technology (NIST) has a wide range of Standard Reference Materials (SRMs) which have values assigned for legacy organic pollutants and toxic elements. Existing SRMs serve as homogenous materials that can be used for method development, meth...

  7. Myths of Isotopic Reference Materials Busted

    NASA Astrophysics Data System (ADS)

    Coplen, T.

    2007-12-01

    During the past several years, the determination of the isotopic abundances of elements including H, Li, B, C, N, O, Mg, Si, S, Cl, Ca, Cr, Fe, Cu, Zn, Tl, and Se has substantially increased because of expanded use in hydrology, environmental studies, microbiology, forensic investigations, atmospheric investigations, oceanography, etc. Improvements in instrumentation enable increasingly precise isotope-amount-ratio measurements in these fields, but these improvements in precision commonly do not lead to improvements in accuracy because of the lack or improper use of isotopic reference materials. When properly used, these critically important materials enable any laboratory worldwide to measure the same homogeneous sample and report the same isotopic abundance within analytical uncertainty. For example, for stable isotopic analysis of gaseous hydrogen samples, the agreement among 36 laboratories worldwide before normalization to any hydrogen gas reference material was 11.8 per mill. After normalization to anchors (gaseous H isotopic reference materials) at each end of the delta H-2 scale, the agreement was 0.85 per mill, an improvement of more than an order of magnitude. Consistency of delta C-13 measurements often can be improved by nearly 50 percent by anchoring the delta C-13 scale with two isotopic reference materials differing substantially in C-13 mole fraction, namely NBS 19 calcite and L-SVEC lithium carbonate. Agreement of delta C-13 values of four expert laboratories analyzing USGS40 L- glutamic acid by CF-IRMS methods improved from 0.084 to 0.015 per mill with use of the two scale anchors (NBS 19 and L-SVEC). Solid oxygen isotopic reference materials (IAEA-600 caffeine, IAEA-601 and IAEA-602 benzoic acids, IAEA-NO-3, USGS32, USGS34, and USGS35 nitrates, NBS-127, IAEA-SO-5, and IAEA-SO-6 barium sulfates) are poorly calibrated. Calibrating these solids to the VSMOW-SLAP reference water scale has been very difficult because both the solids and reference

  8. Compilation of references on geology and hydrology of the Snake River drainage basin above Weiser, Idaho

    USGS Publications Warehouse

    Bassick, M.D.

    1986-01-01

    More than 1,100 references concerning geology and hydrology of the Snake River drainage basin above Weiser, Idaho, are compiled as part of the U.S. Geological Survey 's RASA (Regional Aquifer-System Analysis) study of the Snake River Plain. The list of references is intended as a primary source of information for investigators concerned with previous studies in the basin. Reference numbers correlate with a key-word index to help the user select and locate desired references. (USGS)

  9. Predictive modeling of terrestrial radiation exposure from geologic materials

    NASA Astrophysics Data System (ADS)

    Haber, Daniel A.

    Aerial gamma ray surveys are an important tool for national security, scientific, and industrial interests in determining locations of both anthropogenic and natural sources of radioactivity. There is a relationship between radioactivity and geology and in the past this relationship has been used to predict geology from an aerial survey. The purpose of this project is to develop a method to predict the radiologic exposure rate of the geologic materials in an area by creating a model using geologic data, images from the Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER), geochemical data, and pre-existing low spatial resolution aerial surveys from the National Uranium Resource Evaluation (NURE) Survey. Using these data, geospatial areas, referred to as background radiation units, homogenous in terms of K, U, and Th are defined and the gamma ray exposure rate is predicted. The prediction is compared to data collected via detailed aerial survey by our partner National Security Technologies, LLC (NSTec), allowing for the refinement of the technique. High resolution radiation exposure rate models have been developed for two study areas in Southern Nevada that include the alluvium on the western shore of Lake Mohave, and Government Wash north of Lake Mead; both of these areas are arid with little soil moisture and vegetation. We determined that by using geologic units to define radiation background units of exposed bedrock and ASTER visualizations to subdivide radiation background units of alluvium, regions of homogeneous geochemistry can be defined allowing for the exposure rate to be predicted. Soil and rock samples have been collected at Government Wash and Lake Mohave as well as a third site near Cameron, Arizona. K, U, and Th concentrations of these samples have been determined using inductively coupled mass spectrometry (ICP-MS) and laboratory counting using radiation detection equipment. In addition, many sample locations also have

  10. Reference Materials on the World Wide Web.

    ERIC Educational Resources Information Center

    Kitao, Kenji

    2002-01-01

    This paper presents information about World Wide Web resources for English language teachers and students and for communication scholars and researchers. The first Web page, "Reference Materials for Students and Researchers," offers links to resources in English. Because there are many Web sites related to dictionaries, a second page, "Reference…

  11. 40 CFR 86.1 - Reference materials.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Register approved the incorporation by reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone... § 86.1901. (2) (g) Society of Automotive Engineers (SAE). Anyone may purchase copies of these materials from Society of Automotive Engineers, 400 Commonwealth Dr., Warrendale, PA 15096-0001, (877)...

  12. 40 CFR 1065.1010 - Reference materials.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 4 of this section lists material from the Society of Automotive Engineering that we have... Federal Register approved the incorporation by reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part... Specification for Automotive Spark-Ignition Engine Fuel 1065.701 ASTM D5186-03, Standard Test Method...

  13. Development of Argon Isotope Reference Standards for the U.S. Geological Survey

    PubMed Central

    Miiller, Archie P.

    2006-01-01

    The comparison of physical ages of geological materials measured by laboratories engaged in geochronological studies has been limited by the accuracy of mineral standards or monitors for which reported ages have differed by as much as 2 %. In order to address this problem, the U.S. Geological Survey is planning to calibrate the conventional 40Ar/40K age of a new preparation of an international hornblende standard labeled MMhb-2. The 40K concentration in MMhb-2 has already been determined by the Analytical Chemistry Division at NIST with an uncertainty of 0.2 %. The 40Ar concentration will be measured by the USGS using the argon isotope reference standards that were recently developed by NIST and are described in this paper. The isotope standards were constructed in the form of pipette/reservoir systems and calibrated by gas expansion techniques to deliver small high-precision aliquots of high-purity argon. Two of the pipette systems will deliver aliquots of 38Ar having initial molar quantities of 1.567 × 10−10 moles and 2.313 × 10−10 moles with expanded (k = 2) uncertainties of 0.058 % and 0.054 %, respectively. Three other pipette systems will deliver aliquots (nominally 4 × 10−10 moles) of 40Ar:36Ar artificial mixtures with similar accuracy and with molar ratios of 0.9974 ± 0.06 %, 29.69 ± 0.06 %, and 285.7 ± 0.08 % (k = 2). These isotope reference standards will enable the USGS to measure the 40Ar concentration in MMhb-2 with an expanded uncertainty of ≈ 0.1 %. In the process of these measurements, the USGS will re-determine the isotopic composition of atmospheric Ar and calculate a new value for its atomic weight. Upon completion of the USGS calibrations, the MMhb-2 mineral standard will be certified by NIST for its K and Ar concentrations and distributed as a Standard Reference Material (SRM). The new SRM and the NIST-calibrated transportable pipette systems have the potential for dramatically improving the accuracy of interlaboratory

  14. Development of Argon Isotope Reference Standards for the U.S. Geological Survey.

    PubMed

    Miiller, Archie P

    2006-01-01

    The comparison of physical ages of geological materials measured by laboratories engaged in geochronological studies has been limited by the accuracy of mineral standards or monitors for which reported ages have differed by as much as 2 %. In order to address this problem, the U.S. Geological Survey is planning to calibrate the conventional (40)Ar/(40)K age of a new preparation of an international hornblende standard labeled MMhb-2. The (40)K concentration in MMhb-2 has already been determined by the Analytical Chemistry Division at NIST with an uncertainty of 0.2 %. The (40)Ar concentration will be measured by the USGS using the argon isotope reference standards that were recently developed by NIST and are described in this paper. The isotope standards were constructed in the form of pipette/reservoir systems and calibrated by gas expansion techniques to deliver small high-precision aliquots of high-purity argon. Two of the pipette systems will deliver aliquots of (38)Ar having initial molar quantities of 1.567 × 10(-10) moles and 2.313 × 10(-10) moles with expanded (k = 2) uncertainties of 0.058 % and 0.054 %, respectively. Three other pipette systems will deliver aliquots (nominally 4 × 10(-10) moles) of (40)Ar:(36)Ar artificial mixtures with similar accuracy and with molar ratios of 0.9974 ± 0.06 %, 29.69 ± 0.06 %, and 285.7 ± 0.08 % (k = 2). These isotope reference standards will enable the USGS to measure the (40)Ar concentration in MMhb-2 with an expanded uncertainty of ≈ 0.1 %. In the process of these measurements, the USGS will re-determine the isotopic composition of atmospheric Ar and calculate a new value for its atomic weight. Upon completion of the USGS calibrations, the MMhb-2 mineral standard will be certified by NIST for its K and Ar concentrations and distributed as a Standard Reference Material (SRM). The new SRM and the NIST-calibrated transportable pipette systems have the potential for dramatically improving the accuracy of

  15. Geological and geochemical aspects of uranium deposits: a selected, annotated bibliography. [474 references

    SciTech Connect

    Thomas, J.M.; Garland, P.A.; White, M.B.; Daniel, E.W.

    1980-09-01

    This bibliography, a compilation of 474 references, is the fourth in a series compiled from the National Uranium Resource Evaluation (NURE) Bibliographic Data Base. This data base was created for the Grand Junction Office of the Department of Energy's National Uranium Resource Evaluation Project by the Ecological Sciences Information Center, Oak Ridge National Laboratory. The references in the bibliography are arranged by subject category: (1) geochemistry, (2) exploration, (3) mineralogy, (4) genesis of deposits, (5) geology of deposits, (6) uranium industry, (7) geology of potential uranium-bearing areas, and (8) reserves and resources. The references are indexed by author, geographic location, quadrangle name, geoformational feature, and keyword.

  16. Thermoelectric standardisation - Reference materials and characterisation

    NASA Astrophysics Data System (ADS)

    Ziolkowski, P.; Blaschkewitz, P.; Stiewe, C.; Karpinski, G.; Müller, E.

    2012-06-01

    Thermoelectric materials for working temperatures between 300 K and 1000 K become continuously more important for energy recuperation applications. The efficiency is determined by the transport properties (electrical and thermal conductivity and Seebeck coefficient), which form the known thermoelectric figure of merit ZT. The thorough determination of ZT represents the basis for the assessment of thermoelectric materials research. Due to different continuing difficulties measurement errors distinctly higher than 15% can be observed repeatedly, which is still too high for an industrial benchmark and deficient for many scientific investigations and technological developments. Against this background a project was launched in 2011 together with the Fraunhofer Institute of Physical Measurement Techniques (IPM, Freiburg), the Department Temperature of the Physikalisch-Technische Bundesanstalt (PTB, Berlin) and the company Netzsch Gerätebau GbmH (Selb). The aim of the project "Thermoelectric Standardisation" (TEST) is to minimise the measurement uncertainties and to develop traceable, high-accurate thermoelectric characterisation techniques and thermoelectric reference materials for the mentioned temperature range. Here we initially present the project to the thermoelectric society and want to give a survey on the planned activities and the current status of the contributions of the German Aerospace Center (DLR, Cologne).

  17. Lithium isotope composition of basalt glass reference material.

    PubMed

    Kasemann, Simone A; Jeffcoate, Alistair B; Elliott, Tim

    2005-08-15

    We present data on the lithium isotope compositions of glass reference materials from the United States Geological Survey (USGS) and the National Institute of Standards and Technology (NIST) determined by multicollector inductively coupled plasma mass spectrometry (MC-ICPMS), thermal ionization mass spectrometry (TIMS), and secondary ionization mass spectrometry (SIMS). Our data on the USGS basaltic glass standards agree within 2 per thousand, independent of the sample matrix or Li concentration. For SIMS analysis, we propose use of the USGS glasses GSD-1G (delta(7)Li 31.14 +/- 0.8 per thousand, 2sigma) and BCR-2G (delta(7)Li 4.08 +/- 1.0 per thousand, 2sigma) as suitable standards that cover a wide range of Li isotope compositions. Lithium isotope measurements on the silica-rich NIST 600 glass series by MC-ICPMS and TIMS agree within 0.8 per thousand, but SIMS analyses show systematic isotopic differences. Our results suggest that SIMS Li isotope analyses have a significant matrix bias in high-silica materials. Our data are intended to serve as a reference for both microanalytical and bulk analytical techniques and to improve comparisons between Li isotope data produced by different methodologies.

  18. Value assignment of nutrient concentrations in five standard reference materials and six reference materials.

    PubMed

    Sharpless, K E; Gill, L M

    2000-01-01

    A number of food-matrix reference materials (RMs) are available from the National Institute of Standards and Technology (NIST) and from Agriculture Canada through NIST. Most of these materials were originally value-assigned for their elemental composition (major, minor, and trace elements), but no additional nutritional information was provided. Two of the materials were certified for selected organic constituents. Ten of these materials (Standard Reference Material [SRM] 1,563 Cholesterol and Fat-Soluble Vitamins in Coconut Oil [Natural and Fortified], SRM 1,566b Oyster Tissue, SRM 1,570a Spinach Leaves, SRM 1,974a Organics in Mussel Tissue (Mytilus edulis), RM 8,415 Whole Egg Powder, RM 8,418 Wheat Gluten, RM 8,432 Corn Starch, RM 8,433 Corn Bran, RM 8,435 Whole Milk Powder, and RM 8,436 Durum Wheat Flour) were recently distributed by NIST to 4 laboratories with expertise in food analysis for the measurement of proximates (solids, fat, protein, etc.), calories, and total dietary fiber, as appropriate. SRM 1846 Infant Formula was distributed as a quality control sample for the proximates and for analysis for individual fatty acids. Two of the materials (Whole Egg Powder and Whole Milk Powder) were distributed in an earlier interlaboratory comparison exercise in which they were analyzed for several vitamins. Value assignment of analyte concentrations in these 11 SRMs and RMs, based on analyses by the collaborating laboratories, is described in this paper. These materials are intended primarily for validation of analytical methods for the measurement of nutrients in foods of similar composition (based on AOAC INTERNATIONAL's fat-protein-carbohydrate triangle). They may also be used as "primary control materials" in the value assignment of in-house control materials of similar composition. The addition of proximate information for 10 existing reference materials means that RMs are now available from NIST with assigned values for proximates in 6 of the 9 sectors of

  19. Re-evaluation and extension of the scope of elements in US Geological Survey Standard Reference Water Samples

    USGS Publications Warehouse

    Peart, D.B.; Antweiler, R.C.; Taylor, H.E.; Roth, D.A.; Brinton, T.I.

    1998-01-01

    More than 100 US Geological Survey (USGS) Standard Reference Water Samples (SRWSs) were analyzed for numerous trace constituents, including Al, As, B, Ba, Be, Bi, Br, Cd, Cr, Co, Cu, I, Fe, Pb, Li, Mn, Mo, Ni, Rb, Sb, Se, Sr, Te, Tl, U, V, Zn and major elements (Ca, Mg, Na, SiO2, SO4, Cl) by inductively coupled plasma mass spectrometry and inductively coupled plasma atomic emission spectrometry. In addition, 15 USGS SRWSs and National Institute of Standards and Technology (NIST) standard reference material (SRM) 1641b were analyzed for mercury using cold vapor atomic fluorescence spectrometry. Also USGS SRWS Hg-7 was analyzed using isotope dilution-inductively coupled plasma mass spectrometry. The results were compared with the reported certified values of the following standard reference materials: NIST SRM 1643a, 1643b, 1643c and 1643d and National Research Council of Canada Riverine Water Reference Materials for Trace Metals SLRS-1, SLRS-2 and SLRS-3. New concentration values for trace and major elements in the SRWSs, traceable to the certified standards, are reported. Additional concentration values are reported for elements that were neither previously published for the SRWSs nor traceable to the certified reference materials. Robust statistical procedures were used that were insensitive to outliers. These data can be used for quality assurance/quality control purposes in analytical laboratories.

  20. 40 CFR 90.7 - Reference materials.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies may be inspected at U.S. EPA Air and Radiation... 19103. Document number and name 40 CFR part 90 reference ASTM D86-93: Standard Test Method for...., Warrendale, PA 15096-0001. Document number and name 40 CFR part 90 reference SAE J1930 September...

  1. 40 CFR 90.7 - Reference materials.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies may be inspected at U.S. EPA Air and Radiation... 19103. Document number and name 40 CFR part 90 reference ASTM D86-93: Standard Test Method for...., Warrendale, PA 15096-0001. Document number and name 40 CFR part 90 reference SAE J1930 September...

  2. 40 CFR 91.6 - Reference materials.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...(a) and 1 CFR part 51. Copies may be inspected at U.S. EPA, OAR, Air and Radiation Docket and... 19103. Document number and name 40 CFR part 91 reference ASTM D86-93: Standard Test Method for... 40 CFR part 91 reference SAE J1228/ISO 8665 November 1991 Small Craft-Marine Propulsion Engine...

  3. 40 CFR 91.6 - Reference materials.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...(a) and 1 CFR part 51. Copies may be inspected at U.S. EPA, OAR, Air and Radiation Docket and... 19103. Document number and name 40 CFR part 91 reference ASTM D86-93: Standard Test Method for... 40 CFR part 91 reference SAE J1228/ISO 8665 November 1991 Small Craft-Marine Propulsion Engine...

  4. 40 CFR 91.6 - Reference materials.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...(a) and 1 CFR part 51. Copies may be inspected at U.S. EPA, OAR, Air and Radiation Docket and... 19103. Document number and name 40 CFR part 91 reference ASTM D86-93: Standard Test Method for... 40 CFR part 91 reference SAE J1228/ISO 8665 November 1991 Small Craft-Marine Propulsion Engine...

  5. 40 CFR 90.7 - Reference materials.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies may be inspected at U.S. EPA Air and Radiation... 19103. Document number and name 40 CFR part 90 reference ASTM D86-93: Standard Test Method for...., Warrendale, PA 15096-0001. Document number and name 40 CFR part 90 reference SAE J1930 September...

  6. 40 CFR 90.7 - Reference materials.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies may be inspected at U.S. EPA Air and Radiation... 19103. Document number and name 40 CFR part 90 reference ASTM D86-93: Standard Test Method for...., Warrendale, PA 15096-0001. Document number and name 40 CFR part 90 reference SAE J1930 September...

  7. 40 CFR 92.5 - Reference materials.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... of the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies may be inspected...., Philadelphia, PA 19103. The table follows: Document number and name 40 CFR part 92 reference ASTM D 86-95... follows: Document number and name 40 CFR part 92 reference SAE Paper 770141, Optimization of a...

  8. 40 CFR 91.6 - Reference materials.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...(a) and 1 CFR part 51. Copies may be inspected at U.S. EPA, OAR, Air and Radiation Docket and... 19103. Document number and name 40 CFR part 91 reference ASTM D86-93: Standard Test Method for... 40 CFR part 91 reference SAE J1228/ISO 8665 November 1991 Small Craft-Marine Propulsion Engine...

  9. 40 CFR 90.7 - Reference materials.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies may be inspected at U.S. EPA Air and Radiation... 19103. Document number and name 40 CFR part 90 reference ASTM D86-93: Standard Test Method for...., Warrendale, PA 15096-0001. Document number and name 40 CFR part 90 reference SAE J1930 September...

  10. 40 CFR 92.5 - Reference materials.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... of the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies may be inspected...., Philadelphia, PA 19103. The table follows: Document number and name 40 CFR part 92 reference ASTM D 86-95... follows: Document number and name 40 CFR part 92 reference SAE Paper 770141, Optimization of a...

  11. 40 CFR 91.6 - Reference materials.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...(a) and 1 CFR part 51. Copies may be inspected at U.S. EPA, OAR, Air and Radiation Docket and... 19103. Document number and name 40 CFR part 91 reference ASTM D86-93: Standard Test Method for... 40 CFR part 91 reference SAE J1228/ISO 8665 November 1991 Small Craft-Marine Propulsion Engine...

  12. Determination of carbonate carbon in geological materials by coulometric titration

    USGS Publications Warehouse

    Engleman, E.E.; Jackson, L.L.; Norton, D.R.

    1985-01-01

    A coulometric titration is used for the determination of carbonate carbon in geological materials. Carbon dioxide is evolved from the sample by the addition of 2 M perchloric acid, with heating, and is determined by automated coulometric titration. The coulometric titration showed improved speed and precision with comparable accuracy to gravimetric and gasometric techniques. ?? 1985.

  13. Thermal-infrared spectral observations of geologic materials in emission

    NASA Technical Reports Server (NTRS)

    Christensen, Philip R.; Luth, Sharon J.

    1987-01-01

    The thermal-infrared spectra of geologic materials in emission were studied using the prototype Thermal Emission Spectrometer (TES). A variety of of processes and surface modifications that may influence or alter the spectra of primary rock materials were studied. It was confirmed that thermal emission spectra contain the same absorption features as those observed in transmission and reflection spectra. It was confirmed that the TES instrument can be used to obtain relevant spectra for analysis of rock and mineral composition.

  14. 40 CFR 1065.1010 - Reference materials.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... Federal Register approved the incorporation by reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part... of the International System of Units (SI), Barry N. Taylor, Physics Laboratory 1065.20,...

  15. 40 CFR 89.6 - Reference materials.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 5 U.S.C. 552(a) and 1 CFR part 51. Copies may be inspected at US EPA, OAR, 1200 Pennsylvania Ave... 19428-2959. Document number and name 40 CFR part 89 reference ASTM D86-97: “Standard Test Method for... Commonwealth Dr., Warrendale, PA 15096-0001. Document number and name 40 CFR part 89 reference SAE J244 June...

  16. 40 CFR 89.6 - Reference materials.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 5 U.S.C. 552(a) and 1 CFR part 51. Copies may be inspected at US EPA, OAR, 1200 Pennsylvania Ave... 19428-2959. Document number and name 40 CFR part 89 reference ASTM D86-97: “Standard Test Method for... Commonwealth Dr., Warrendale, PA 15096-0001. Document number and name 40 CFR part 89 reference SAE J244 June...

  17. Electrostatic aggregation of finely-comminuted geological materials

    NASA Technical Reports Server (NTRS)

    Marshall, J. R.; Greeley, R.

    1986-01-01

    Electrostatic forces are known to have a significant effect on the behavior of finely comminuted particulate material: perhaps the most prevalent expression of this being electrostatic aggregation of particles into relatively coherent clumps. However, the precise role of electrostatic attraction and repulsion in determining the behavior of geological materials (such as volcanic ash and aeolian dust) is poorly understood. Electrostatic aggregation of fine particles is difficult to study on Earth either in the geological or laboratory environment principally because the material in an aggregated state remains airborne for such a short period of time. Experiments conducted in the NASA/JCS - KC135 aircraft are discussed. The aircraft experiments are seen as precursors to more elaborate and scientifically more comprehensive Shuttle or Space Station activities.

  18. Electrostatic aggregation of finely-comminuted geological materials

    NASA Technical Reports Server (NTRS)

    Marshall, John R.; Greeley, Ronald

    1987-01-01

    Electrostatic forces are known to have a significant effect on the behavior of finely comminuted particulate material: perhaps the most prevalent expression of this being electrostatic aggregation of particles into relatively coherent clumps. However, the precise role of electrostatic attraction and repulsion in determining the behavior of geological materials (such as volcanic ash and aeolian dust) is poorly understood. Electrostatic aggregation of fine particles is difficult to study on earth either in the geological or laboratory environment principally because the material in an aggregated state remains airborne for such a short period of time. Experiments conducted in the NASA/JSC - KC135 aircraft are discussed. The aircraft experiments are seen as precursors to more elaborate and scientifically more comprehensive Shuttle or Space Station activities.

  19. New Carbonate Standard Reference Materials for Boron Isotope Geochemistry

    NASA Astrophysics Data System (ADS)

    Stewart, J.; Christopher, S. J.; Day, R. D.

    2015-12-01

    The isotopic composition of boron (δ11B) in marine carbonates is well established as a proxy for past ocean pH. Yet, before palaeoceanographic interpretation can be made, rigorous assessment of analytical uncertainty of δ11B data is required; particularly in light of recent interlaboratory comparison studies that reported significant measurement disagreement between laboratories [1]. Well characterised boron standard reference materials (SRMs) in a carbonate matrix are needed to assess the accuracy and precision of carbonate δ11B measurements throughout the entire procedural chemistry; from sample cleaning, to ionic separation of boron from the carbonate matrix, and final δ11B measurement by multi-collector inductively coupled plasma mass spectrometry. To date only two carbonate reference materials exist that have been value-assigned by the boron isotope measurement community [2]; JCp-1 (porites coral) and JCt-1 (Giant Clam) [3]. The National Institute of Standards and Technology (NIST) will supplement these existing standards with new solution based inorganic carbonate boron SRMs that replicate typical foraminiferal and coral B/Ca ratios and δ11B values. These new SRMs will not only ensure quality control of full procedural chemistry between laboratories, but have the added benefits of being both in abundant supply and free from any restrictions associated with shipment of biogenic samples derived from protected species. Here we present in-house δ11B measurements of these new boron carbonate SRM solutions. These preliminary data will feed into an interlaboratory comparison study to establish certified values for these new NIST SRMs. 1. Foster, G.L., et al., Chemical Geology, 2013. 358(0): p. 1-14. 2. Gutjahr, M., et al., Boron Isotope Intercomparison Project (BIIP): Development of a new carbonate standard for stable isotopic analyses. Geophysical Research Abstracts, EGU General Assembly 2014, 2014. 16(EGU2014-5028-1). 3. Inoue, M., et al., Geostandards and

  20. Reproducibility of polycarbonate reference material in toxicity evaluation

    NASA Technical Reports Server (NTRS)

    Hilado, C. J.; Huttlinger, P. A.

    1981-01-01

    A specific lot of bisphenol A polycarbonate has been used for almost four years as the reference material for the NASA-USF-PSC toxicity screening test method. The reproducibility of the test results over this period of time indicate that certain plastics may be more suitable reference materials than the more traditional cellulosic materials.

  1. Expanded Subject Access to Reference Collection Materials.

    ERIC Educational Resources Information Center

    Mischo, William H.

    1979-01-01

    Reports a computer assisted index emphasizing expanded subject access to the reference collection of the Iowa State University Library. The index displays abbreviated length records and complements existing catalogs. Limitations of subject access and a system for assigning subject descriptors are discussed. (Author/RAA)

  2. 40 CFR 1042.910 - Reference materials.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone may inspect copies at the U.S. EPA, Air... Embankment, London SE1 7SR, United Kingdom, or http://www.imo.org, or 44-(0)20-7735-7611. (1) Revised...

  3. 40 CFR 1042.910 - Reference materials.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone may inspect copies at the U.S. EPA, Air... Embankment, London SE1 7SR, United Kingdom, or http://www.imo.org, or 44-(0)20-7735-7611. (1) Revised...

  4. AOAC INTERNATIONAL's Technical Division on Reference Materials (TDRM) Reference Materials Database.

    PubMed

    Zink, Donna

    2016-09-01

    The Technical Division on Reference Materials (TDRM) of AOAC INTERNATIONAL recommends policy and criteria to facilitate the development and use of reference materials (RMs) in the validation, implementation, and routine use of AOAC INTERNATIONAL methods. To aid analysts in these areas, TDRM has developed a searchable online database to identify RMs suitable for use with AOAC Official Methods of Analysis(SM) (OMA). RMs can be queried by analyte, by analyte and matrix, or by the selection of an OMA, based on analytes and matrixes described within the scope of the selected method. Only essential information is included in the database, to maximize usefulness and minimize the effort required to keep information current. Additional information, such as measurement uncertainty and purchasing instructions, is available through a link to the producer's Web site, when that information is available online. Data sets are solicited on a voluntary basis from National Metrology Institutes and accredited producers. Consideration of ease-of-use and ease-of-operation is a guiding principle in this database, as is cost management. PMID:27619655

  5. delta 15N and non-carbonate delta 13C values for two petroleum source rock reference materials and a marine sediment reference material

    USGS Publications Warehouse

    Dennen, Kristin O.; Johnson, Craig A.; Otter, Marshall L.; Silva, Steven R.; Wandless, Gregory A.

    2006-01-01

    Samples of United States Geological Survey (USGS) Certified Reference Materials USGS Devonian Ohio Shale (SDO-1), and USGS Eocene Green River Shale (SGR-1), and National Research Council Canada (NRCC) Certified Marine Sediment Reference Material (PACS-2), were sent for analysis to four separate analytical laboratories as blind controls for organic rich sedimentary rock samples being analyzed from the Red Dog mine area in Alaska. The samples were analyzed for stable isotopes of carbon (delta13Cncc) and nitrogen (delta15N), percent non-carbonate carbon (Wt % Cncc) and percent nitrogen (Wt % N). SDO-1, collected from the Huron Member of the Ohio Shale, near Morehead, Kentucky, and SGR-1, collected from the Mahogany zone of the Green River Formation are petroleum source rocks used as reference materials for chemical analyses of sedimentary rocks. PACS-2 is modern marine sediment collected from the Esquimalt, British Columbia harbor. The results presented in this study are, with the exceptions noted below, the first published for these reference materials. There are published information values for the elemental concentrations of 'organic' carbon (Wt % Corg measured range is 8.98 - 10.4) and nitrogen (Wt % Ntot 0.347 with SD 0.043) only for SDO-1. The suggested values presented here should be considered 'information values' as defined by the NRCC Institute for National Measurement Reference Materials and should be useful for the analysis of 13C, 15N, C and N in organic material in sedimentary rocks.

  6. Corrosion reference for geothermal downhole materials selection

    SciTech Connect

    Ellis, P.F. II, Smith, C.C.; Keeney, R.C.; Kirk, D.K.; Conover, M.F.

    1983-03-01

    Geothermal downhole conditions that may affect the performance and reliability of selected materials and components used in the drilling, completion, logging, and production of geothermal wells are reviewed. The results of specific research and development efforts aimed at improvement of materials and components for downhole contact with the hostile physicochemical conditions of the geothermal reservoir are discussed. Materials and components covered are tubular goods, stainless steels and non-ferrous metals for high-temperature downhole service, cements for high-temperature geothermal wells, high-temperature elastomers, drilling and completion tools, logging tools, and downhole pumps. (MHR)

  7. Single And Multiple Jet Penetration Experiments Into Geologic Materials

    SciTech Connect

    Kuklo, R; Murphy, M J; Rambur, T A; Switzer, L L; Summers, M A

    2003-12-19

    This paper presents the results of experiments that investigate the effect of single and multiple jet penetration into geologic materials. In previous studies of jet penetration into concrete targets, we demonstrated that an enhanced surface crater could be created by the simultaneous penetration of multiple shaped charge jets and that an enhanced target borehole could be created by the subsequent delayed penetration of a single shaped charge jet. This paper describes an extension of the multiple jet penetration research to limestone and granite.

  8. LA-ICP-MS of magnetite: Methods and reference materials

    USGS Publications Warehouse

    Nadoll, P.; Koenig, A.E.

    2011-01-01

    Magnetite (Fe3O4) is a common accessory mineral in many geologic settings. Its variable geochemistry makes it a powerful petrogenetic indicator. Electron microprobe (EMPA) analyses are commonly used to examine major and minor element contents in magnetite. Laser ablation ICP-MS (LA-ICP-MS) is applicable to trace element analyses of magnetite but has not been widely employed to examine compositional variations. We tested the applicability of the NIST SRM 610, the USGS GSE-1G, and the NIST SRM 2782 reference materials (RMs) as external standards and developed a reliable method for LA-ICP-MS analysis of magnetite. LA-ICP-MS analyses were carried out on well characterized magnetite samples with a 193 nm, Excimer, ArF LA system. Although matrix-matched RMs are sometimes important for calibration and normalization of LA-ICP-MS data, we demonstrate that glass RMs can produce accurate results for LA-ICP-MS analyses of magnetite. Cross-comparison between the NIST SRM 610 and USGS GSE-1G indicates good agreement for magnetite minor and trace element data calibrated with either of these RMs. Many elements show a sufficiently good match between the LA-ICP-MS and the EMPA data; for example, Ti and V show a close to linear relationship with correlation coefficients, R2 of 0.79 and 0.85 respectively. ?? 2011 The Royal Society of Chemistry.

  9. 15 CFR 200.104 - Standard reference materials.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ..., PROCEDURES, AND FEES § 200.104 Standard reference materials. Often the performance of a device or structure...-characterized materials that are needed to calibrate a measurement system or to produce scientific data that...

  10. 40 CFR 86.1 - Reference materials.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Director of the Federal Register under 5 U.S.C. 552(a) and 1 CFR part 51. To enforce any edition other than... materials may be obtained from Society of Automotive Engineers International, 400 Commonwealth Dr..., Methane Measurement Using Gas Chromatography, 1994 SAE Handbook—SAE International Cooperative...

  11. 10 CFR 431.105 - Materials incorporated by reference.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 10 Energy 3 2013-01-01 2013-01-01 false Materials incorporated by reference. 431.105 Section 431.105 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL... Storage Tanks Test Procedures § 431.105 Materials incorporated by reference. (a) General. DOE...

  12. 10 CFR 431.105 - Materials incorporated by reference.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 10 Energy 3 2012-01-01 2012-01-01 false Materials incorporated by reference. 431.105 Section 431.105 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL... Storage Tanks Test Procedures § 431.105 Materials incorporated by reference. (a) The...

  13. 10 CFR 431.105 - Materials incorporated by reference.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 10 Energy 3 2014-01-01 2014-01-01 false Materials incorporated by reference. 431.105 Section 431.105 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL... Storage Tanks Test Procedures § 431.105 Materials incorporated by reference. (a) General. DOE...

  14. Corrosion reference for geothermal downhole materials selection: Overview

    SciTech Connect

    Ellis, Peter F.

    1982-10-08

    A consolidated reference of materials for downhole equipment used in geothermal energy exploitation is nearing completion. The reference is a summary of recent developments in the areas of tubular goods materials, highly alloyed metals, high temperature cements, high temperature elastomers, drilling and completion tools, logging tools, and downwell pumps. A brief overview is presented in this paper.

  15. Multi-Elemental Nuclear Analysis of soil reference material

    NASA Astrophysics Data System (ADS)

    Metairon, S.; Zamboni, C. B.; Medeiros, I. M. M. Amaral; Menezes, M. À. B. C.

    2011-08-01

    The elements concentration in the soil reference material (IAEA/SOIL-7) was obtained using the parametric Neutron Activation Analysis technique in the IEA-R1 nuclear reactor at IPEN (CNEN-SP). The results obtained were in good agreement with the respective nominal values from this reference material suggesting the viability of using this parametric procedure for environmental investigations.

  16. Predictive Modeling of Terrestrial Radiation Exposure from Geologic Materials

    SciTech Connect

    Malchow, Russell L.; Haber, Daniel University of Nevada, Las Vegas; Burnley, Pamela; Marsac, Kara; Hausrath, Elisabeth; Adcock, Christopher

    2015-01-01

    Aerial gamma ray surveys are important for those working in nuclear security and industry for determining locations of both anthropogenic radiological sources and natural occurrences of radionuclides. During an aerial gamma ray survey, a low flying aircraft, such as a helicopter, flies in a linear pattern across the survey area while measuring the gamma emissions with a sodium iodide (NaI) detector. Currently, if a gamma ray survey is being flown in an area, the only way to correct for geologic sources of gamma rays is to have flown the area previously. This is prohibitively expensive and would require complete national coverage. This project’s goal is to model the geologic contribution to radiological backgrounds using published geochemical data, GIS software, remote sensing, calculations, and modeling software. K, U and Th are the three major gamma emitters in geologic material. U and Th are assumed to be in secular equilibrium with their daughter isotopes. If K, U, and Th abundance values are known for a given geologic unit the expected gamma ray exposure rate can be calculated using the Grasty equation or by modeling software. Monte Carlo N-Particle Transport software (MCNP), developed by Los Alamos National Laboratory, is modeling software designed to simulate particles and their interactions with matter. Using this software, models have been created that represent various lithologies. These simulations randomly generate gamma ray photons at energy levels expected from natural radiologic sources. The photons take a random path through the simulated geologic media and deposit their energy at the end of their track. A series of nested spheres have been created and filled with simulated atmosphere to record energy deposition. Energies deposited are binned in the same manner as the NaI detectors used during an aerial survey. These models are used in place of the simplistic Grasty equation as they take into account absorption properties of the lithology which the

  17. [Review of normal spectral emissivity standard reference materials].

    PubMed

    Yu, Kun; Liu, Yu-Fang; Zhao, Yue-Jin

    2012-11-01

    In order to improve the accuracy of spectral emissivity measurement, standard reference materials of spectral emissivity as the dissemination of quantity in spectral emissivity measurement are used for the calibration of spectral emissivity measurement apparatus. In the present paper, firstly the standard reference materials data proposed by the American National Institute of Standards and Technology are introduced, and some underlying standard reference materials suggested by some metering departments in Europe are analyzed in detail For the standard reference material Armco iron and SiC proposed by some researchers, the advantages and disadvantages were explored. Finally, the characteristics of standard reference materials are summarized, and the future development of spectral emissivity measurement standard is prospected.

  18. USE OF NATURAL WATERS AS U. S. GEOLOGICAL SURVEY REFERENCE SAMPLES.

    USGS Publications Warehouse

    Janzer, Victor J.

    1985-01-01

    The U. S. Geological Survey conducts research and collects hydrologic data relating to the Nation's water resources. Seven types of natural matrix reference water samples are prepared for use in the Survey's quality assurance program. These include samples containing major constituents, trace metals, nutrients, herbicides, insecticides, trace metals in a water and suspended-sediment mixture, and precipitation (snowmelt). To prepare these reference samples, natural water is collected in plastic drums and the sediment is allowed to settle. The water is then filtered, selected constituents are added, and if necessary the water is acidified and sterilized by ultraviolet irradiation before bottling in plastic or glass. These reference samples are distributed twice yearly to more than 100 laboratories for chemical analysis. The most probable values for each constituent are determined by evaluating the data submitted by the laboratories using statistical techniques recommended by ASTM.

  19. Geology

    SciTech Connect

    Reidel, Stephen P.

    2008-01-17

    This chapter summarizes the geology of the single-shell tank (SST) farms in the context of the region’s geologic history. This chapter is based on the information in the geology data package for the SST waste management areas and SST RFI Appendix E, which builds upon previous reports on the tank farm geology and Integrated Disposal Facility geology with information available after those reports were published.

  20. The sorption of polonium, actinium and protactinium onto geological materials

    SciTech Connect

    Baston, G.M.N.; Berry, J.A.; Brownsword, M.; Heath, T.G.; Ilett, D.J.; McCrohon, R.; Tweed, C.J.; Yui, M.

    1999-07-01

    This paper describes a combined experimental and modeling program of generic sorption studies to increase confidence in the performance assessment for a potential high-level radioactive waste repository in Japan. The sorption of polonium, actinium and protactinium onto geological materials has been investigated. Sorption of these radioelements onto bentonite, tuff and granodiorite from equilibrated de-ionized water was studied under reducing conditions at room temperature. In addition, the sorption of actinium and protactinium was investigated at 60 C. Thermodynamic chemical modeling was carried out to aid interpretation of the results.

  1. ISOTOPIC COMPOSITIONS OF URANIUM REFERENCE MATERIALS

    SciTech Connect

    Jacobsen, B; Borg, L; Williams, R; Brennecka, G; Hutcheon, I

    2009-09-03

    Uranium isotopic compositions of a variety of U standard materials were measured at Lawrence Livermore National Laboratory and are reported here. Both thermal ionization mass spectrometry (TIMS) and multi-collector inductively couple plasma mass spectrometry (MC-ICPMS) were used to determine ratios of the naturally occurring isotopes of U. Establishing an internally coherent set of isotopic values for a range of U standards is essential for inter-laboratory comparison of small differences in {sup 238}U/{sup 235}U, as well as the minor isotopes of U. Differences of {approx} 1.3{per_thousand} are now being observed in {sup 238}U/{sup 235}U in natural samples, and may play an important role in understanding U geochemistry where tracing the origin of U is aided by U isotopic compositions. The {sup 238}U/{sup 235}U ratios were measured with a TRITON TIMS using a mixed {sup 233}U-{sup 236}U isotopic tracer to correct for instrument fractionation. this tracer was extremely pure and resulted in only very minor corrections on the measured {sup 238}U/{sup 235}U ratios of {approx} 0.03. The values obtained for {sup 238}U/{sup 235}U are: IRMM184 = 137.698 {+-} 0.020 (n = 15), SRM950a = 137.870 {+-} 0.018 (n = 8), and CRM112a = 137.866 {+-} 0.030 (n = 16). Uncertainties represent 2 s.d. of the population. The measured value for IRMM184 is in near-perfect agreement with the certified value of 137.697 {+-} 0.042. However, the U isotopic compositions of SRM950a and CRM112a are not certified. Minor isotopes of U were determined with a Nu Plasma HR MC-ICPMS and mass bias was corrected by sample/standard bracketing to IRMM184, using its certified {sup 238}U/{sup 235}U ratio. Thus, the isotopic compositions determined using both instruments are compatible. The values obtained for {sup 234}U/{sup 235}U are: SRM950a = (7.437 {+-} 0.043) x 10{sup -3} (n = 18), and CRM112a = (7.281 {+-} 0.050) x 10{sup -3} (n = 16), both of which are in good agreement with published values. The value for

  2. Teaching about Asia: Professional Materials and Reference Books.

    ERIC Educational Resources Information Center

    Hantula, James N.

    This two-part document serves as a guide to basic materials on Asia. The first part provides the teacher of Asian studies with nonserial examples of pertinent professional materials and reference books in print since 1979. Criteria used in selecting the items are given and a brief comparison between materials available in 1969 and 1985 is made.…

  3. Progress in Value Assignment for Stable Isotope Reference Materials

    NASA Astrophysics Data System (ADS)

    Gröning, M.; Taylor, P. D.; Klinedinst, D. B.

    2001-05-01

    A re-compilation of the existing certificate data for stable isotope reference materials was carried out at IAEA during the last years. Most of these isotopic ratios are expressed as per mil deviation relative to the isotopic ratio of an artificially chosen primary reference material using the commonly used conventional δ -scales. The recommended isotope values for those reference materials, produced by various researchers and institutions over the last four decades and distributed by the IAEA and NIST, have been subject to different `value assignment' approaches in the past and resulted in some inconsistencies in their recommended certified isotopic composition. During an IAEA Advisory Group meeting in September 2000 consensus was obtained on a consistent and robust a posteriori data evaluation to assign the value on the existing whole suite of stable isotope reference materials (RM) for the elements of hydrogen, carbon, nitrogen, oxygen and sulfur. Advances towards a closer calibration of carbon RMs were presented by NIST as a result of a performed calibration exercise for inorganic stable carbon RMs involving selected laboratories. For the first time sulfur stable isotope calibration data were presented by different institutions, which allow a firm and consistent value assignment of sulfur stable isotope RMs. At the same time efforts at IRMM were presented to tie up those conventional δ -scale values to SI-units by direct isotope ratio measurements using primary methods. The future challenges are twofold: 1. improving and maintaining the consistency of established stable isotope δ -scales by better characterization of existing reference materials and production of suitable successor materials (as example the primary water reference materials VSMOW and SLAP will be discussed), and 2. producing suitable reference materials for new analytical methods, especially in the field of organic compounds analyzed by means of continuous flow methods involving gas

  4. 40 CFR 194.13 - Submission of reference materials.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... COMPLIANCE WITH THE 40 CFR PART 191 DISPOSAL REGULATIONS Compliance Certification and Re-certification... and Santa Fe, New Mexico. Reference materials that are widely available in standard text books...

  5. 40 CFR 194.13 - Submission of reference materials.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... COMPLIANCE WITH THE 40 CFR PART 191 DISPOSAL REGULATIONS Compliance Certification and Re-certification... and Santa Fe, New Mexico. Reference materials that are widely available in standard text books...

  6. 40 CFR 194.13 - Submission of reference materials.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... COMPLIANCE WITH THE 40 CFR PART 191 DISPOSAL REGULATIONS Compliance Certification and Re-certification... and Santa Fe, New Mexico. Reference materials that are widely available in standard text books...

  7. Laboratory Reference Spectroscopy of Icy Satellite Candidate Surface Materials (Invited)

    NASA Astrophysics Data System (ADS)

    Dalton, J. B.; Jamieson, C. S.; Shirley, J. H.; Pitman, K. M.; Kariya, M.; Crandall, P.

    2013-12-01

    The bulk of our knowledge of icy satellite composition continues to be derived from ultraviolet, visible and infrared remote sensing observations. Interpretation of remote sensing observations relies on availability of laboratory reference spectra of candidate surface materials. These are compared directly to observations, or incorporated into models to generate synthetic spectra representing mixtures of the candidate materials. Spectral measurements for the study of icy satellites must be taken under appropriate conditions (cf. Dalton, 2010; also http://mos.seti.org/icyworldspectra.html for a database of compounds) of temperature (typically 50 to 150 K), pressure (from 10-9 to 10-3 Torr), viewing geometry, (i.e., reflectance), and optical depth (must manifest near infrared bands but avoid saturation in the mid-infrared fundamentals). The Planetary Ice Characterization Laboratory (PICL) is being developed at JPL to provide robust reference spectra for icy satellite surface materials. These include sulfate hydrates, hydrated and hydroxylated minerals, and both organic and inorganic volatile ices. Spectral measurements are performed using an Analytical Spectral Devices FR3 portable grating spectrometer from .35 to 2.5 microns, and a Thermo-Nicolet 6500 Fourier-Transform InfraRed (FTIR) spectrometer from 1.25 to 20 microns. These are interfaced with the Basic Extraterrestrial Environment Simulation Testbed (BEEST), a vacuum chamber capable of pressures below 10-9 Torr with a closed loop liquid helium cryostat with custom heating element capable of temperatures from 30-800 Kelvins. To generate optical constants (real and imaginary index of refraction) for use in nonlinear mixing models (i.e., Hapke, 1981 and Shkuratov, 1999), samples are ground and sieved to six different size fractions or deposited at varying rates to provide a range of grain sizes for optical constants calculations based on subtractive Kramers-Kronig combined with Hapke forward modeling (Dalton and

  8. Characterization of a diet reference material for 17 elements

    SciTech Connect

    Miller-Ihli, N.J.; Wolf, W.R.

    1986-12-01

    A freeze-dried diet reference material was prepared from commonly consumed everyday foods. Concentrations of major (Mg, Ca, Na, K and P), minor (Mn, Zn, Fe, Cu, and Al), and trace elements (Cr, Ni, Co, Mo, As, Se, and Cd) in this diet material were determined by the authors and 10 collaborating laboratories using a total of 10 different analytical techniques. Good agreement between concentration values determined by the different laboratories enabled the authors to computer recommended values and uncertainties for these 17 elements. Values for proximates as well as several other nutrients were also reported by collaborators. This diet material is available to the scientific community as Reference Material 8431 through the National Bureau of Standard's Office of Standard Reference Materials.

  9. Certified reference materials and reference methods for nuclear safeguards and security.

    PubMed

    Jakopič, R; Sturm, M; Kraiem, M; Richter, S; Aregbe, Y

    2013-11-01

    Confidence in comparability and reliability of measurement results in nuclear material and environmental sample analysis are established via certified reference materials (CRMs), reference measurements, and inter-laboratory comparisons (ILCs). Increased needs for quality control tools in proliferation resistance, environmental sample analysis, development of measurement capabilities over the years and progress in modern analytical techniques are the main reasons for the development of new reference materials and reference methods for nuclear safeguards and security. The Institute for Reference Materials and Measurements (IRMM) prepares and certifices large quantities of the so-called "large-sized dried" (LSD) spikes for accurate measurement of the uranium and plutonium content in dissolved nuclear fuel solutions by isotope dilution mass spectrometry (IDMS) and also develops particle reference materials applied for the detection of nuclear signatures in environmental samples. IRMM is currently replacing some of its exhausted stocks of CRMs with new ones whose specifications are up-to-date and tailored for the demands of modern analytical techniques. Some of the existing materials will be re-measured to improve the uncertainties associated with their certified values, and to enable laboratories to reduce their combined measurement uncertainty. Safeguards involve the quantitative verification by independent measurements so that no nuclear material is diverted from its intended peaceful use. Safeguards authorities pay particular attention to plutonium and the uranium isotope (235)U, indicating the so-called 'enrichment', in nuclear material and in environmental samples. In addition to the verification of the major ratios, n((235)U)/n((238)U) and n((240)Pu)/n((239)Pu), the minor ratios of the less abundant uranium and plutonium isotopes contain valuable information about the origin and the 'history' of material used for commercial or possibly clandestine purposes, and

  10. 10 CFR 431.263 - Materials incorporated by reference.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... paragraph (b) of this section for incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Any subsequent amendment to this material by the standard-setting organization will not affect... Society for Testing and Materials (ASTM) Standard F2324-03, “Standard Test Method for Prerinse...

  11. Preparation and characterization of ``exhausted electrowinning electrolyte'' reference material

    NASA Astrophysics Data System (ADS)

    Arana, G.; Amigo, J. M.; Etxebarria, N.; Fernandez, L. A.; Raposo, J. C.

    2003-05-01

    The number of available reference materials of complex matrices is continuously growing but it is still far from ideal. There are too many different matrices which are of interest for too many different analytes. The certified reference materials are expensive and are intended for the validation of methods or for the assurance of traceability of the analytical result. However, many determinations are carried out on a daily basis and the quality control for these determinations requires the use of reference materials, although not certified but laboratory reference materials. These materials are not certified but must be homogeneous and stable with respect to the concentration of the analytes of interest and they must have a similar matrix compared to the samples to be analysed, in order to be able to perform the quality control of the analytical determinations. The reference material herein presented is an exhausted electrowinning electrolyte from a local copper producing company. The analytical determination of the metals in the solution was performed using ICP-AES with a multivariate calibration procedure. The analytes are the following : As, Ca, Cu, Fe, Na, Ni, Sb and Zn.

  12. Reference materials--a main element in a coherent reference measurement system.

    PubMed

    Dybkaer, R

    1991-04-01

    The analytical reliability of any measurement procedure requires a specifically designed, coherent reference measurement system, including interrelated measurement procedures and measurement standards such as reference materials. The latter may be characterized by three sets of characteristics. The general characteristics comprise origin, mode of production, physical state and phase, homogeneity, physical form, container, additives, storage conditions, stability, and dangerous properties. The specific characteristics describe molecular composition, analyte, purity, matrix, quantity of interest (including scale), assigned value, and uncertainty of measurement. The additional characteristics concern the way in which values for other characteristics were obtained, the hierarchical position of the material, certificate, instructions for use, and intended function. The problem areas of reference materials comprise definition of the appropriate analyte, purification, matrix, assignment of values, and nomenclature. The present ambiguous terminology is presented and a systematic structure of descriptive names is proposed (tab. 1). PMID:1868129

  13. [Study on certified reference material of iodine in kelp].

    PubMed

    Lu, Longgen; Qian, Yaling; Lu, Xiujing

    2004-09-01

    Analytical reference material of iodine in kelp was designed and prepared for accurate analysis, monitor and evaluation of iodine in trade of farming, forestry, medicine and food hygiene can be used in technical training, technical assessing, monitoring, date arbitrating and analytic method verifying for professional supervisors. This reference material was certified by neutron activation, ICP-MS, PA, GC, IC, COL method. According to Gurbb's law to judge the date of each group, it was confirmed that all of six groups certified curde date were normal distribution by checking normality D. The arithmetic mean value of all data on certified reference material of low and moderate amount was 9.3 microg/g and 85.7 microg/g respectively and, standard deviation was 0.9 microg/g and 4.9 microg/g respectively.

  14. Selenium Preconcentration in Geological Materials for Determination at sub-μ g\\ g-1 Concentration

    NASA Astrophysics Data System (ADS)

    Bedard, L. P.

    2004-05-01

    Selenium is important because it is a path finder element in economic geology. It has similar geochemical properties as sulfur, but slightly less mobile and less volatile in sulfides. Although its environmental cycle is better understood, its geological cycle is almost unknown. In geological samples, Se concentration ranges 0,02-1 μ g\\ g-1. Se has many spectral interefences in ICP-MS, rendering difficult to determine. INAA detection limit for geological samples is about 10 μ g\\ g-1. The analytical difficulties are one of the main reason why the geological cycle of Se is so poorly known. The preconcentration of Se with Thiol Cotton Fiber (TCF) followed by atomic absorption (AA) has been modified to be used with INAA. The modified technique involves sample dissolution (HF-HNO3) and evaporation to dryness at low temperature (55-60 oC) to keep Se in solution. Se is converted to SeIV by adding 5-6 mol l-1 HCl and heating covered in a boiling bath (95-100oC). Sample is diluted with deionized water to obtain 0,3 - 1 mol l-1 HCl and then collected on TCF. TCF is put in a polyethylene vial for irradiation in the SLOWPOKE II reactor for 10 seconds at a neutron flux of 1015 m-2 s-1. The 162 KeV peak of 77Se (half-life 17,36 sec) is read for 20 seconds after a decay of 7 seconds. Results for certified reference materials show the TCF preconcentration technique followed by INAA provides results comparable with AA with a detection limit of approximately 0,05 μ g\\ g-1. Moreover INAA provides many advantages such as eliminating the desorption step and is less time consuming than AA.

  15. SPOTS project and development of a standard and reference material

    NASA Astrophysics Data System (ADS)

    Burguete, R.; Patterson, E.

    2010-06-01

    The ‘Standardization Project for Optical Techniques of Strain measurement’ (SPOTS) was focused on the development of reference materials for calibrating optical systems for static strain measurement and standardized tests for evaluating the capabilities of such systems. The reference material consists of a beam in four-point bending within a monolithic frame that ensures reproducibility of the boundary and loading conditions. A procedure for the use of the reference material has been developed and leads to the evaluation of measurement uncertainties that allow the construction of confidence limits for the data obtained with the calibrated optical system. The design and methodology have been developed into a proposed draft standard which is being endorsed by VAMAS (Versailles Agreement on Materials And Standards) for review by ISO (International Standards Organisation). An overview of philosophy underpinning the proposed draft standard is presented and serves as an introduction to the reference material and standardized test and their use in providing higher confidence in optical measurements of strain.

  16. Production and characterization of a bovine liver candidate reference material

    NASA Astrophysics Data System (ADS)

    Bianchi, S. R.; Peixoto, A. M. J.; Souza, G. B.; Tullio, R. R.; Nogueira, A. R. A.

    2016-07-01

    The preparation of a bovine liver candidate reference material and the steps are taken to confirm its homogeneity, long and short term stabilities, and consensus values are described. Details of the sample preparation and the final collaborative exercise are presented. The material elemental composition was characterized by 17 elements (As, Ca, Cd, Co, Cu, Fe, K, Mg, Mo, Mn, Na, P, Pb, Se, Sr, V, and Zn) of nutritional and toxicological significance.

  17. Developing a matrix reference material for screening of transgenic rice.

    PubMed

    Li, Jun; Wu, Yuhua; Li, Xiaofei; Wang, Yulei; Zhang, Li; Li, Yunjing; Wu, Gang

    2015-12-01

    Certified reference materials (CRMs) that are compatible with detection methods are needed to detect genetically modified organisms (GMOs). Screening is the first detection step in determining the possible presence of GMO ingredients in food or feed; however, screening has been hindered by the lack of GMO CRMs. In this study, transgenic rice materials were developed via the transformation of a construct harboring 11 commonly used screening elements. Digital PCR was utilized to identify a homozygous single-copy line termed SDrice. The qualitative detections of 11 elements in 21 transgenic materials demonstrated that the genomic DNA of the SDrice was suitable for use as a positive control in the screening of GMO ingredients. The suitability of SDrice as reference material was further checked by testing the sensitivity of 11 known conventional PCR assays, ranging from 10 to 50 copies of the SDrice genome. The standard curves that were created using SDrice DNA series as calibrators all exhibited good linearities in the relationships of the Ct values with the template copy numbers in these 11 real-time PCR assays. The LODs of the real-time PCR assays were estimated to be two to five copies of the SDrice genome. Comparisons of the SDrice with other GM rice revealed that significant differences existed in both the intercepts of the standard curves and the ΔCt values of the exogenous and reference genes for the P-35S, T-nos, HPT, T-35S, and Bar assays; the SDrice was not fit for quantification of other GM rice events. This study provided a matrix reference material (RM) that was suitable for screening GM rice, determination of sensitivity and a LOD of PCR assays, and overcame some of the drawbacks of plasmid DNA as reference material. PMID:26462921

  18. Developing a matrix reference material for screening of transgenic rice.

    PubMed

    Li, Jun; Wu, Yuhua; Li, Xiaofei; Wang, Yulei; Zhang, Li; Li, Yunjing; Wu, Gang

    2015-12-01

    Certified reference materials (CRMs) that are compatible with detection methods are needed to detect genetically modified organisms (GMOs). Screening is the first detection step in determining the possible presence of GMO ingredients in food or feed; however, screening has been hindered by the lack of GMO CRMs. In this study, transgenic rice materials were developed via the transformation of a construct harboring 11 commonly used screening elements. Digital PCR was utilized to identify a homozygous single-copy line termed SDrice. The qualitative detections of 11 elements in 21 transgenic materials demonstrated that the genomic DNA of the SDrice was suitable for use as a positive control in the screening of GMO ingredients. The suitability of SDrice as reference material was further checked by testing the sensitivity of 11 known conventional PCR assays, ranging from 10 to 50 copies of the SDrice genome. The standard curves that were created using SDrice DNA series as calibrators all exhibited good linearities in the relationships of the Ct values with the template copy numbers in these 11 real-time PCR assays. The LODs of the real-time PCR assays were estimated to be two to five copies of the SDrice genome. Comparisons of the SDrice with other GM rice revealed that significant differences existed in both the intercepts of the standard curves and the ΔCt values of the exogenous and reference genes for the P-35S, T-nos, HPT, T-35S, and Bar assays; the SDrice was not fit for quantification of other GM rice events. This study provided a matrix reference material (RM) that was suitable for screening GM rice, determination of sensitivity and a LOD of PCR assays, and overcame some of the drawbacks of plasmid DNA as reference material.

  19. 9 CFR 77.1 - Material incorporated by reference.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. (a) The procedures... AGRICULTURE INTERSTATE TRANSPORTATION OF ANIMALS (INCLUDING POULTRY) AND ANIMAL PRODUCTS TUBERCULOSIS General Provisions § 77.1 Material incorporated by reference. Uniform Methods and Rules—Bovine...

  20. 9 CFR 77.1 - Material incorporated by reference.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. (a) The procedures... AGRICULTURE INTERSTATE TRANSPORTATION OF ANIMALS (INCLUDING POULTRY) AND ANIMAL PRODUCTS TUBERCULOSIS General Provisions § 77.1 Material incorporated by reference. Uniform Methods and Rules—Bovine...

  1. 9 CFR 77.1 - Material incorporated by reference.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. (a) The procedures... AGRICULTURE INTERSTATE TRANSPORTATION OF ANIMALS (INCLUDING POULTRY) AND ANIMAL PRODUCTS TUBERCULOSIS General Provisions § 77.1 Material incorporated by reference. Uniform Methods and Rules—Bovine...

  2. 9 CFR 77.1 - Material incorporated by reference.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. (a) The procedures... AGRICULTURE INTERSTATE TRANSPORTATION OF ANIMALS (INCLUDING POULTRY) AND ANIMAL PRODUCTS TUBERCULOSIS General Provisions § 77.1 Material incorporated by reference. Uniform Methods and Rules—Bovine...

  3. 9 CFR 77.1 - Material incorporated by reference.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. (a) The procedures... AGRICULTURE INTERSTATE TRANSPORTATION OF ANIMALS (INCLUDING POULTRY) AND ANIMAL PRODUCTS TUBERCULOSIS General Provisions § 77.1 Material incorporated by reference. Uniform Methods and Rules—Bovine...

  4. APEX (Air Pollution Exercise) Volume 20: Reference Materials.

    ERIC Educational Resources Information Center

    Environmental Protection Agency, Research Triangle Park, NC. Office of Manpower Development.

    The Reference Materials Manual is part of a set of 21 manuals (AA 001 009-001 029) used in APEX (Air Pollution Exercise), a computerized college and professional level "real world" game simulation of a community with urban and rural problems, industrial activities, and air pollution difficulties. For the purposes of the gaming exercise, APEX…

  5. 10 CFR 431.75 - Materials incorporated by reference.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR 51. Any subsequent amendment to this... INDUSTRIAL EQUIPMENT Commercial Warm Air Furnaces Test Procedures § 431.75 Materials incorporated by..., “Gas-Fired Central Furnaces,” IBR approved for § 431.76. (2) Underwriters Laboratories (UL)...

  6. 10 CFR 431.133 - Materials incorporated by reference.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 10 Energy 3 2011-01-01 2011-01-01 false Materials incorporated by reference. 431.133 Section 431.133 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL.... Department of Energy, Forrestal Building, Room 1J-018 (Resource Room of the Building Technologies...

  7. 10 CFR 431.263 - Materials incorporated by reference.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 10 Energy 3 2011-01-01 2011-01-01 false Materials incorporated by reference. 431.263 Section 431.263 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL... to: http://www.archives.gov/federal-register/cfr/ibr-locations.html. (ii) U.S. Department of...

  8. 10 CFR 431.203 - Materials incorporated by reference.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 10 Energy 3 2010-01-01 2010-01-01 false Materials incorporated by reference. 431.203 Section 431.203 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL... of Energy, Forrestal Building, Room 1J-018 (Resource Room of the Building Technologies Program),...

  9. 10 CFR 431.293 - Materials incorporated by reference.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    .... Department of Energy, Office of Energy Efficiency and Renewable Energy, Building Technologies Program, 6th... 10 Energy 3 2010-01-01 2010-01-01 false Materials incorporated by reference. 431.293 Section 431.293 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN...

  10. 10 CFR 431.263 - Materials incorporated by reference.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 10 Energy 3 2010-01-01 2010-01-01 false Materials incorporated by reference. 431.263 Section 431.263 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL... to: http://www.archives.gov/federal-register/cfr/ibr-locations.html. (ii) U.S. Department of...

  11. 10 CFR 431.203 - Materials incorporated by reference.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 10 Energy 3 2011-01-01 2011-01-01 false Materials incorporated by reference. 431.203 Section 431.203 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL... of Energy, Forrestal Building, Room 1J-018 (Resource Room of the Building Technologies Program),...

  12. 10 CFR 431.223 - Materials incorporated by reference.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 10 Energy 3 2010-01-01 2010-01-01 false Materials incorporated by reference. 431.223 Section 431.223 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL.... Department of Energy, Forrestal Building, Room 1J-018 (Resource Room of the Building Technologies...

  13. 10 CFR 431.63 - Materials incorporated by reference.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    .... Department of Energy, Office of Energy Efficiency and Renewable Energy, Building Technologies Program, 6th... 10 Energy 3 2011-01-01 2011-01-01 false Materials incorporated by reference. 431.63 Section 431.63 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL...

  14. 10 CFR 431.75 - Materials incorporated by reference.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 10 Energy 3 2011-01-01 2011-01-01 false Materials incorporated by reference. 431.75 Section 431.75 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL AND.... Department of Energy, Office of Energy Efficiency and Renewable Energy, Hearings and Dockets,...

  15. 10 CFR 431.293 - Materials incorporated by reference.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    .... Department of Energy, Office of Energy Efficiency and Renewable Energy, Building Technologies Program, 6th... 10 Energy 3 2011-01-01 2011-01-01 false Materials incorporated by reference. 431.293 Section 431.293 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN...

  16. 10 CFR 431.63 - Materials incorporated by reference.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    .... Department of Energy, Office of Energy Efficiency and Renewable Energy, Building Technologies Program, 6th... 10 Energy 3 2010-01-01 2010-01-01 false Materials incorporated by reference. 431.63 Section 431.63 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL...

  17. 10 CFR 431.75 - Materials incorporated by reference.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 10 Energy 3 2010-01-01 2010-01-01 false Materials incorporated by reference. 431.75 Section 431.75 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL AND.... Department of Energy, Office of Energy Efficiency and Renewable Energy, Hearings and Dockets,...

  18. 10 CFR 431.223 - Materials incorporated by reference.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 10 Energy 3 2011-01-01 2011-01-01 false Materials incorporated by reference. 431.223 Section 431.223 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL.... Department of Energy, Forrestal Building, Room 1J-018 (Resource Room of the Building Technologies...

  19. Analysis of standard reference materials by absolute INAA

    SciTech Connect

    Heft, R.E.; Koszykowski, R.F.

    1981-07-01

    Three standard reference materials, flyash, soil, and ASI 4340 steel, were analyzed by a method of absolute instrumental neutron activation analysis (INAA). Two different light water pool-type reactors were used to produce equivalent analytical results even though the epithermal to thermal flux ratio in one reactor was higher than that in the other by a factor of two.

  20. 40 CFR 194.13 - Submission of reference materials.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 26 2012-07-01 2011-07-01 true Submission of reference materials. 194.13 Section 194.13 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) RADIATION PROTECTION PROGRAMS CRITERIA FOR THE CERTIFICATION AND RE-CERTIFICATION OF THE WASTE ISOLATION PILOT PLANT'S COMPLIANCE WITH THE 40 CFR PART...

  1. 10 CFR 431.263 - Materials incorporated by reference.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... paragraph (b) of this section for incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR... Society for Testing and Materials (ASTM) Standard F2324-03, “Standard Test Method for Prerinse Spray... to: http://www.archives.gov/federal-register/cfr/ibr-locations.html. (ii) U.S. Department of...

  2. 10 CFR 431.133 - Materials incorporated by reference.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... paragraph (b) of this section for incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Any subsequent amendment to this material by the standard-setting organization will not affect... Ice-Makers.” (2) American National Standards Institute (ANSI)/American Society of...

  3. 10 CFR 431.63 - Materials incorporated by reference.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 10 Energy 3 2014-01-01 2014-01-01 false Materials incorporated by reference. 431.63 Section 431.63 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL AND... Director of the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR 51. Any subsequent...

  4. 10 CFR 431.85 - Materials incorporated by reference.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ...., Washington, DC 20024, 202-586-2945, or go to: http://www1.eere.energy.gov/buildings/appliance_standards... 10 Energy 3 2012-01-01 2012-01-01 false Materials incorporated by reference. 431.85 Section 431.85 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL...

  5. 10 CFR 431.85 - Materials incorporated by reference.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ...., Washington, DC 20024, 202-586-2945, or go to: http://www1.eere.energy.gov/buildings/appliance_standards... 10 Energy 3 2014-01-01 2014-01-01 false Materials incorporated by reference. 431.85 Section 431.85 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL...

  6. 10 CFR 431.63 - Materials incorporated by reference.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 10 Energy 3 2012-01-01 2012-01-01 false Materials incorporated by reference. 431.63 Section 431.63 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL AND... Director of the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR 51. Any subsequent...

  7. 10 CFR 431.293 - Materials incorporated by reference.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... Floor, 950 L'Enfant Plaza, SW., Washington, DC 20024, 202-586-2945, or visit http://www1.eere.energy.gov... 10 Energy 3 2014-01-01 2014-01-01 false Materials incorporated by reference. 431.293 Section 431.293 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN...

  8. 10 CFR 431.293 - Materials incorporated by reference.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... Floor, 950 L'Enfant Plaza, SW., Washington, DC 20024, 202-586-2945, or visit http://www1.eere.energy.gov... 10 Energy 3 2012-01-01 2012-01-01 false Materials incorporated by reference. 431.293 Section 431.293 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN...

  9. 10 CFR 431.63 - Materials incorporated by reference.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 10 Energy 3 2013-01-01 2013-01-01 false Materials incorporated by reference. 431.63 Section 431.63 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL AND... Director of the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR 51. Any subsequent...

  10. 10 CFR 431.85 - Materials incorporated by reference.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ...., Washington, DC 20024, 202-586-2945, or go to: http://www1.eere.energy.gov/buildings/appliance_standards... 10 Energy 3 2013-01-01 2013-01-01 false Materials incorporated by reference. 431.85 Section 431.85 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL...

  11. 10 CFR 431.223 - Materials incorporated by reference.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    .... 552(a) and 1 CFR part 51. Any subsequent amendment to this material by the standard-setting... procedures incorporated by reference. (1) Environmental Protection Agency, “ENERGY STAR Program Requirements... Agency “ENERGY STAR Program Requirements for Traffic Signals,” Version 1.1, may be obtained from...

  12. Digestion of titanium bearing geologic materials involving microwaves.

    PubMed

    Tripathi, Anju; Chattopadhyay, Partha

    2007-10-01

    An environmentally friendly and rapid digestion procedure involving 10 mL of acid mixture (HNO3 : HCl : HF = 2:2:1) for 0.1 g of sample in closed vessel microwave digester following heating program : 250W for 10 min., hold time 2 min., 600 W for 17 min, and Ventilation time 10 min was developed. The operating parameters were varied and optimized by factorial design approach using "Steepest Ascent" method. The validity of the recommended digestion procedure were examined by analyzing several well characterized standard reference materials such as diabase (W2), basalt (BIR-1, JB-3, BHVO-1), granite (G2), gabbro (JGb-1), Mn-nodule (Nod-A-1, Nod-P-1), sediment (STSD-4, LKSD-2), limestone (KH-2), soil (SAu-1), ilmenite (IGS-31), rutile (IGS-32), Zircon (IGS-35) and titanium dioxide (SRM-154b) employing both inductively coupled plasma-atomic emission spectrometry (ICP-AES) and well known spectrophotometric method. An excellent agreement between the methods and the certified values of standard reference materials suggest that the digestion procedure can be used for quality control and allied purposes.

  13. Digestion of titanium bearing geologic materials involving microwaves.

    PubMed

    Tripathi, Anju; Chattopadhyay, Partha

    2007-10-01

    An environmentally friendly and rapid digestion procedure involving 10 mL of acid mixture (HNO3 : HCl : HF = 2:2:1) for 0.1 g of sample in closed vessel microwave digester following heating program : 250W for 10 min., hold time 2 min., 600 W for 17 min, and Ventilation time 10 min was developed. The operating parameters were varied and optimized by factorial design approach using "Steepest Ascent" method. The validity of the recommended digestion procedure were examined by analyzing several well characterized standard reference materials such as diabase (W2), basalt (BIR-1, JB-3, BHVO-1), granite (G2), gabbro (JGb-1), Mn-nodule (Nod-A-1, Nod-P-1), sediment (STSD-4, LKSD-2), limestone (KH-2), soil (SAu-1), ilmenite (IGS-31), rutile (IGS-32), Zircon (IGS-35) and titanium dioxide (SRM-154b) employing both inductively coupled plasma-atomic emission spectrometry (ICP-AES) and well known spectrophotometric method. An excellent agreement between the methods and the certified values of standard reference materials suggest that the digestion procedure can be used for quality control and allied purposes. PMID:18153999

  14. Full vector low-temperature magnetic measurements of geologic materials

    NASA Astrophysics Data System (ADS)

    Feinberg, Joshua M.; Solheid, Peter A.; Swanson-Hysell, Nicholas L.; Jackson, Mike J.; Bowles, Julie A.

    2015-01-01

    magnetic properties of geologic materials offer insights into an enormous range of important geophysical phenomena ranging from inner core dynamics to paleoclimate. Often it is the low-temperature behavior (<300 K) of magnetic minerals that provides the most useful and highest sensitivity information for a given problem. Conventional measurements of low-temperature remanence are typically conducted on instruments that are limited to measuring one single-axis component of the magnetization vector and are optimized for measurements in strong fields. These instrumental limitations have prevented fully optimized applications and have motivated the development of a low-temperature probe that can be used for low-temperature remanence measurements between 17 and 300 K along three orthogonal axes using a standard 2G Enterprises SQuID rock magnetometer. In this contribution, we describe the design and implementation of this instrument and present data from five case studies that demonstrate the probe's considerable potential for future research: a polycrystalline hematite sample, a polycrystalline hematite and magnetite mixture, a single crystal of magnetite, a single crystal of pyrrhotite, and samples of Umkondo Large Igneous Province diabase sills.

  15. High-precision isotopic characterization of USGS reference materials by TIMS and MC-ICP-MS

    NASA Astrophysics Data System (ADS)

    Weis, Dominique; Kieffer, Bruno; Maerschalk, Claude; Barling, Jane; de Jong, Jeroen; Williams, Gwen A.; Hanano, Diane; Pretorius, Wilma; Mattielli, Nadine; Scoates, James S.; Goolaerts, Arnaud; Friedman, Richard M.; Mahoney, J. Brian

    2006-08-01

    The Pacific Centre for Isotopic and Geochemical Research (PCIGR) at the University of British Columbia has undertaken a systematic analysis of the isotopic (Sr, Nd, and Pb) compositions and concentrations of a broad compositional range of U.S. Geological Survey (USGS) reference materials, including basalt (BCR-1, 2; BHVO-1, 2), andesite (AGV-1, 2), rhyolite (RGM-1, 2), syenite (STM-1, 2), granodiorite (GSP-2), and granite (G-2, 3). USGS rock reference materials are geochemically well characterized, but there is neither a systematic methodology nor a database for radiogenic isotopic compositions, even for the widely used BCR-1. This investigation represents the first comprehensive, systematic analysis of the isotopic composition and concentration of USGS reference materials and provides an important database for the isotopic community. In addition, the range of equipment at the PCIGR, including a Nu Instruments Plasma MC-ICP-MS, a Thermo Finnigan Triton TIMS, and a Thermo Finnigan Element2 HR-ICP-MS, permits an assessment and comparison of the precision and accuracy of isotopic analyses determined by both the TIMS and MC-ICP-MS methods (e.g., Nd isotopic compositions). For each of the reference materials, 5 to 10 complete replicate analyses provide coherent isotopic results, all with external precision below 30 ppm (2 SD) for Sr and Nd isotopic compositions (27 and 24 ppm for TIMS and MC-ICP-MS, respectively). Our results also show that the first- and second-generation USGS reference materials have homogeneous Sr and Nd isotopic compositions. Nd isotopic compositions by MC-ICP-MS and TIMS agree to within 15 ppm for all reference materials. Interlaboratory MC-ICP-MS comparisons show excellent agreement for Pb isotopic compositions; however, the reproducibility is not as good as for Sr and Nd. A careful, sequential leaching experiment of three first- and second-generation reference materials (BCR, BHVO, AGV) indicates that the heterogeneity in Pb isotopic compositions

  16. Lawrence Livermore National Laboratory Working Reference Material Production Pla

    SciTech Connect

    Wong, Amy; Thronas, Denise; Marshall, Robert

    1998-11-04

    This Lawrence Livermore National Laboratory (LLNL) Working Reference Material Production Plan was written for LLNL by the Los Alamos National Laboratory to address key elements of producing seven Pu-diatomaceous earth NDA Working Reference Materials (WRMS). These WRMS contain low burnup Pu ranging in mass from 0.1 grams to 68 grams. The composite Pu mass of the seven WRMS was designed to approximate the maximum TRU allowable loading of 200 grams Pu. This document serves two purposes: first, it defines all the operations required to meet the LLNL Statement of Work quality objectives, and second, it provides a record of the production and certification of the WRMS. Guidance provided in ASTM Standard Guide C1128-89 was used to ensure that this Plan addressed all the required elements for producing and certifying Working Reference Materials. The Production Plan was written to provide a general description of the processes, steps, files, quality control, and certification measures that were taken to produce the WRMS. The Plan identifies the files where detailed procedures, data, quality control, and certification documentation and forms are retained. The Production Plan is organized into three parts: a) an initial section describing the preparation and characterization of the Pu02 and diatomaceous earth materials, b) middle sections describing the loading, encapsulation, and measurement on the encapsulated WRMS, and c) final sections describing the calculations of the Pu, Am, and alpha activity for the WRMS and the uncertainties associated with these quantities.

  17. Reference Materials for Reactor Neutron Fluence Rate and Temperature Measurements

    NASA Astrophysics Data System (ADS)

    Ingelbrecht, C.

    2003-06-01

    Certified reference materials are distributed by the European Commission through the BCR® programme (over 500 CRMs) including a series of activation and fission monitor materials originally proposed by the Euratom Working Group on Reactor Dosimetry. The current range (18 CRMs) includes materials to cover the complete energy spectrum, and suitable for different irradiation times. Fission monitors are 238UO2 or 237NpO2 in the form of microspheres. Activation monitors are high purity metals (Ni, Cu, Al, Fe, Nb, Rh, or Ti), certified for interfering trace impurities, or dilute aluminium-based alloys. Reference materials newly certified are IRMM-530R A1-0.1%Au, replacing the exhausted IRMM-530 material, used as comparator for k0- standardisation, and three new Al-Co alloys (0.01, 0.1 and 1.0%Co). Others in the process of certification are A1-0.1%Ag and A1-2%Sc for thermal and epithermal fluence rate measurements and two uranium-doped glass materials intended for dosimetry by the fission-track technique. Various alloy compositions have been prepared for use as melt-wire temperature monitors with melting points ranging from 198 to 327ºC.

  18. Geology

    NASA Technical Reports Server (NTRS)

    Stewart, R. K.; Sabins, F. F., Jr.; Rowan, L. C.; Short, N. M.

    1975-01-01

    Papers from private industry reporting applications of remote sensing to oil and gas exploration were presented. Digitally processed LANDSAT images were successfully employed in several geologic interpretations. A growing interest in digital image processing among the geologic user community was shown. The papers covered a wide geographic range and a wide technical and application range. Topics included: (1) oil and gas exploration, by use of radar and multisensor studies as well as by use of LANDSAT imagery or LANDSAT digital data, (2) mineral exploration, by mapping from LANDSAT and Skylab imagery and by LANDSAT digital processing, (3) geothermal energy studies with Skylab imagery, (4) environmental and engineering geology, by use of radar or LANDSAT and Skylab imagery, (5) regional mapping and interpretation, and digital and spectral methods.

  19. Developing Potential New Reference Materials for Light Isotopes in Foodstuffs

    NASA Astrophysics Data System (ADS)

    Frew, Russell; Van Hale, Robert; Clarke, Dianne; Abrahim, Aiman; Resch, Christian; Mayr, Leopold; Cannavan, Andrew; Gröning, Manfred

    2013-04-01

    Measurements of subtle variations in stable isotope ratios provide the means for verifying food integrity in numerous ways. Adulterants usually have different isotopic composition so their presence in a food is readily detectable. Stable isotope measurements can also be used to determine the region of production of the food. In most cases the ability of stable isotope measurements to verify, or otherwise reject, the authenticity of the food is greatly enhanced by comparison of a result to a reference database. The more high-quality data in the database, the more statistical power is afforded by the comparison. A serious weakness at present is the lack of reference materials in food matrices available to the community. Thus researchers have to rely on in-house standards for calibration and quality assurance. The result is that there are numerous datasets published that may be internally consistent but it is exceedingly difficult to combine these datasets into a cohesive database. This is particularly important for measurements of the hydrogen isotopes. Here we present a survey of the stable isotope (^2H, ^13C and ^15N) composition of 12 Reference Materials from the International Atomic Energy Agency catalogue. All but one of these materials are plant matter and have been developed as reference materials for other applications such as radionuclide or trace element measurements. Thus they have been verified as suitable materials in terms of stability and homogeneity for those tests. The purpose of this work is to ascertain if they are similarly suitable as stable isotope reference materials. The results from our survey show that there is a wide range in elemental and isotopic composition among these materials. For example, the ^15N values range from-13.5‰ to +18.6‰ and the nitrogen elemental composition range is from 0.7% to 9.7%. The ^13C values range from -20‰ to -40‰ and the carbon elemental composition ranges from 15% to 47%. We are now in the process of

  20. Preparation and stability of milk somatic cell reference materials.

    PubMed

    Di Marzo, Larissa; Wojciechowski, Karen L; Barbano, David M

    2016-09-01

    Our objectives were to develop a method to produce milk somatic cell count (SCC) reference materials for calibration of electronic somatic cell count (ESCC) using gravity separation and to determine the effect of refrigerated storage (4°C) and freeze-thaw stability of the skim and whole milk SCC reference materials. Whole raw milk was high-temperature short-time pasteurized and split into 2 portions. One portion was gravity separated at 4°C for 22 h and the second portion was centrifugally separated to produce skim milk that was also gravity separated with somatic cells rising to the surface. After 22 h, stock solutions (low SCC skim milk, high SCC skim milk, high SCC whole milk) were prepared and preserved (bronopol). Two experiments were conducted, one to compare the shelf-life of skim and whole milk SCC standards at 4°C and one to determine the effect of freezing and thawing on SCC standards. Both experiments were replicated 3 times. Gravity separation was an effective approach to isolate and concentrate somatic cells from bovine milk and redistribute them in a skim or whole milk matrix to create a set of reference materials with a wider and more uniformly distributed range of SCC than current calibration sets. The liquid SCC reference materials stored using the common industry practice at 4°C were stable (i.e., fit for purpose, no large decrease in SCC) for a 2-wk period, whereas frozen and thawed reference materials may have a much longer useful life. A gradual decrease occurred in residual difference in ESCC (SCC × 1,000/mL) versus original assigned reference SCC over duration of refrigerated storage for both skim and whole milk SCC samples, indicating that milk ESCC of the preserved milks was gradually decreasing during 28 d of storage at 4°C by about 15,000 SCC/mL. No difference in the ESCC for skim milk was detected between refrigerated and frozen storage, whereas for whole milk the ESCC for frozen was lower than refrigerated samples. Future work is

  1. Preparation and stability of milk somatic cell reference materials.

    PubMed

    Di Marzo, Larissa; Wojciechowski, Karen L; Barbano, David M

    2016-09-01

    Our objectives were to develop a method to produce milk somatic cell count (SCC) reference materials for calibration of electronic somatic cell count (ESCC) using gravity separation and to determine the effect of refrigerated storage (4°C) and freeze-thaw stability of the skim and whole milk SCC reference materials. Whole raw milk was high-temperature short-time pasteurized and split into 2 portions. One portion was gravity separated at 4°C for 22 h and the second portion was centrifugally separated to produce skim milk that was also gravity separated with somatic cells rising to the surface. After 22 h, stock solutions (low SCC skim milk, high SCC skim milk, high SCC whole milk) were prepared and preserved (bronopol). Two experiments were conducted, one to compare the shelf-life of skim and whole milk SCC standards at 4°C and one to determine the effect of freezing and thawing on SCC standards. Both experiments were replicated 3 times. Gravity separation was an effective approach to isolate and concentrate somatic cells from bovine milk and redistribute them in a skim or whole milk matrix to create a set of reference materials with a wider and more uniformly distributed range of SCC than current calibration sets. The liquid SCC reference materials stored using the common industry practice at 4°C were stable (i.e., fit for purpose, no large decrease in SCC) for a 2-wk period, whereas frozen and thawed reference materials may have a much longer useful life. A gradual decrease occurred in residual difference in ESCC (SCC × 1,000/mL) versus original assigned reference SCC over duration of refrigerated storage for both skim and whole milk SCC samples, indicating that milk ESCC of the preserved milks was gradually decreasing during 28 d of storage at 4°C by about 15,000 SCC/mL. No difference in the ESCC for skim milk was detected between refrigerated and frozen storage, whereas for whole milk the ESCC for frozen was lower than refrigerated samples. Future work is

  2. Determination of the rare-earth elements in geological materials by inductively coupled plasma mass spectrometry

    USGS Publications Warehouse

    Lichte, F.E.; Meier, A.L.; Crock, J.G.

    1987-01-01

    A method of analysis of geological materials for the determination of the rare-earth elements using the Inductively coupled plasma mass spectrometric technique (ICP-MS) has been developed. Instrumental parameters and factors affecting analytical results have been first studied and then optimized. Samples are analyzed directly following an acid digestion, without the need for separation or preconcentration with limits of detection of 2-11 ng/g, precision of ?? 2.5% relative standard deviation, and accuracy comparable to inductively coupled plasma emission spectrometry and instrumental neutron activation analysis. A commercially available ICP-MS instrument is used with modifications to the sample introduction system, torch, and sampler orifice to reduce the effects of high salt content of sample solutions prepared from geologic materials. Corrections for isobaric interferences from oxide ions and other diatomic and triatomic ions are made mathematically. Special internal standard procedures are used to compensate for drift in metahmetal oxide ratios and sensitivity. Reference standard values are used to verify the accuracy and utility of the method.

  3. Primary certification of reference material for electrolytic conductivity of bioethanol

    NASA Astrophysics Data System (ADS)

    da Silva, L. F.; Gomes, M. R. F.; Cassini, G. C.; Faria, A. C. V.; Fraga, I. C. S.

    2016-07-01

    Nowadays the preservation of the planet is spreading into the international scene with the use of renewable energy sources such as bioethanol. The challenge is to guarantee the quality of produced bioethanol, and the electrolytic conductivity (EC) is one of the specified parameters for this purpose. However, is necessary to demonstrate the metrological traceability of the measurement results for EC in this matrix. This study presents the certification of a reference material for EC in bioethanol by using only primary measurements. The value of primary certified reference material (CRM) is (0.77 ± 0.06) µS.cm-1, and its use will provide the metrological traceability needed for measurement results in laboratories.

  4. Homogeneity study of candidate reference material in fish matrix

    NASA Astrophysics Data System (ADS)

    Ulrich, J. C.; Sarkis, J. E. S.; Hortellani, M. A.

    2015-01-01

    A material is perfectly homogeneous with respect to a given characteristic, or composition, if there is no difference between the values obtained from one part to another. Homogeneity is usually evaluated using analysis of variance (ANOVA). However, the requirement that populations of data to be processed must have a normal distribution and equal variances greatly limits the use of this statistical tool. A more suitable test for assessing the homogeneity of RMs, known as "sufficient homogeneity", was proposed by Fearn and Thompson. In this work, we evaluate the performance of the two statistical treatments for assessing homogeneity of methylmercury (MeHg) in candidate reference material of fish tissue.

  5. Clinical Biospecimens: Reference Materials, Certified for Nominal Properties?

    PubMed Central

    2014-01-01

    This report makes the case for clinical biospecimens to be certified for nominal properties, in particular the diagnosis, and to attain the level of Reference Materials. Clinical certified biospecimens that are collected, processed, characterized, stored, and distributed by biobanks are urgently needed to facilitate diagnostic test development, evaluation, and quality assurance. Four examples are provided to illustrate this purpose and the certification approaches that could be applied are proposed. PMID:24749878

  6. 10 CFR 431.15 - Materials incorporated by reference.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... material listed for incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Any... §§ 431.12; 431.19; 431.20; appendix B to subpart B of part 431. (2) (c) IEC. International Electrotechnical Commission Central Office, 3, rue de Varembé, P.O. Box 131, CH-1211 GENEVA 20, Switzerland, +41...

  7. Results of the U.S. Geological Survey's Analytical Evaluation Program for Standard Reference Samples Distributed in March 2000

    USGS Publications Warehouse

    Farrar, Jerry W.; Copen, Ashley M.

    2000-01-01

    This report presents the results of the U.S. Geological Survey's analytical evaluation program for six standard reference samples -- T-161 (trace constituents), M-154 (major constituents), N-65 (nutrient constituents), N-66 nutrient constituents), P-34 (low ionic strength constituents), and Hg-30 (mercury) -- that were distributed in March 2000 to 144 laboratories enrolled in the U.S. Geological Survey sponsored interlaboratory testing program. Analytical data that were received from 132 of the laboratories were evaluated with respect to overall laboratory performance and relative laboratory performance for each analyte in the six reference samples. Results of these evaluations are presented in tabular form. Also presented are tables and graphs summarizing the analytical data provided by each laboratory for each analyte in the six standard reference samples. The most probable value for each analyte was determined using nonparametric statistics.

  8. Results of the U. S. Geological Survey's analytical evaluation program for standard reference samples distributed in October 2000

    USGS Publications Warehouse

    Connor, B.F.; Currier, J.P.; Woodworth, M.T.

    2001-01-01

    This report presents the results of the U.S. Geological Survey's analytical evaluation program for six standard reference samples -- T-163 (trace constituents), M-156 (major constituents), N-67 (nutrient constituents), N-68 (nutrient constituents), P-35 (low ionic strength constituents), and Hg-31 (mercury) -- that were distributed in October 2000 to 126 laboratories enrolled in the U.S. Geological Survey sponsored interlaboratory testing program. Analytical data that were received from 122 of the laboratories were evaluated with respect to overall laboratory performance and relative laboratory performance for each analyte in the six reference samples. Results of these evaluations are presented in tabular form. Also presented are tables and graphs summarizing the analytical data provided by each laboratory for each analyte in the six standard reference samples. The most probable value for each analyte was determined using nonparametric statistics.

  9. Results of the U. S. Geological Survey's analytical evaluation program for standard reference samples distributed in April 2001

    USGS Publications Warehouse

    Woodworth, M.T.; Connor, B.F.

    2001-01-01

    This report presents the results of the U.S. Geological Survey's analytical evaluation program for six standard reference samples -- T-165 (trace constituents), M-158 (major constituents), N-69 (nutrient constituents), N-70 (nutrient constituents), P-36 (low ionic-strength constituents), and Hg-32 (mercury) -- that were distributed in April 2001 to laboratories enrolled in the U.S. Geological Survey sponsored interlaboratory testing program. Analytical data received from 73 laboratories were evaluated with respect to overall laboratory performance and relative laboratory performance for each analyte in the six reference samples. Results of these evaluations are presented in tabular form. Also presented are tables and graphs summarizing the analytical data provided by each laboratory for each analyte in the six standard reference samples. The most probable value for each analyte was determined using nonparametric statistics.

  10. Results of the U.S. Geological Survey's Analytical Evaluation Program for standard reference samples distributed in March 1999

    USGS Publications Warehouse

    Farrar, Jerry W.; Chleboun, Kimberly M.

    1999-01-01

    This report presents the results of the U.S. Geological Survey's analytical evaluation program for 8 standard reference samples -- T-157 (trace constituents), M-150 (major constituents), N-61 (nutrient constituents), N-62 (nutrient constituents), P-32 (low ionic strength constituents), GWT-5 (ground-water trace constituents), GWM- 4 (ground-water major constituents),and Hg-28 (mercury) -- that were distributed in March 1999 to 120 laboratories enrolled in the U.S. Geological Survey sponsored interlaboratory testing program. Analytical data that were received from 111 of the laboratories were evaluated with respect to overall laboratory performance and relative laboratory performance for each analyte in the seven reference samples. Results of these evaluations are presented in tabular form. Also presented are tables and graphs summarizing the analytical data provided by each laboratory for each analyte in the 8 standard reference samples. The most probable value for each analyte was determined using nonparametric statistics.

  11. Results of the U.S. Geological Survey's analytical evaluation program for standard reference samples distributed in September 2002

    USGS Publications Warehouse

    Woodworth, Mark T.; Connor, Brooke F.

    2003-01-01

    This report presents the results of the U.S. Geological Survey's analytical evaluation program for six standard reference samples -- T-171 (trace constituents), M-164 (major constituents), N-75 (nutrient constituents), N-76 (nutrient constituents), P-39 (low ionic-strength constituents), and Hg-35 (mercury) -- that were distributed in September 2002 to laboratories enrolled in the U.S. Geological Survey sponsored interlaboratory testing program. Analytical data received from 102 laboratories were evaluated with respect to overall laboratory performance and relative laboratory performance for each analyte in the six reference samples. Results of these evaluations are presented in tabular form. Also presented are tables and graphs summarizing the analytical data provided by each laboratory for each analyte in the six standard reference samples. The most probable value for each analyte was determined using nonparametric statistics.

  12. Results of the U.S. Geological Survey's analytical evaluation program for standard reference samples distributed in March 2003

    USGS Publications Warehouse

    Woodworth, Mark T.; Connor, Brooke F.

    2003-01-01

    This report presents the results of the U.S. Geological Survey's analytical evaluation program for six standard reference samples -- T-173 (trace constituents), M-166 (major constituents), N-77 (nutrient constituents), N-78 (nutrient constituents), P-40 (low ionic-strength constituents), and Hg-36 (mercury) -- that were distributed in March 2003 to laboratories enrolled in the U.S. Geological Survey sponsored interlaboratory testing program. Analytical data received from 110 laboratories were evaluated with respect to overall laboratory performance and relative laboratory performance for each analyte in the six reference samples. Results of these evaluations are presented in tabular form. Also presented are tables and graphs summarizing the analytical data provided by each laboratory for each analyte in the six standard reference samples. The most probable value for each analyte was determined using nonparametric statistics.

  13. Results of the U.S. Geological Survey's analytical evaluation program for standard reference samples distributed in September 2001

    USGS Publications Warehouse

    Woodworth, Mark T.; Connor, Brooke F.

    2002-01-01

    This report presents the results of the U.S. Geological Survey's analytical evaluation program for six standard reference samples -- T-167 (trace constituents), M-160 (major constituents), N-71 (nutrient constituents), N-72 (nutrient constituents), P-37 (low ionic-strength constituents), and Hg-33 (mercury) -- that were distributed in September 2001 to laboratories enrolled in the U.S. Geological Survey sponsored interlaboratory testing program. Analytical data received from 98 laboratories were evaluated with respect to overall laboratory performance and relative laboratory performance for each analyte in the six reference samples. Results of these evaluations are presented in tabular form. Also presented are tables and graphs summarizing the analytical data provided by each laboratory for each analyte in the six standard reference samples. The most probable value for each analyte was determined using nonparametric statistics.

  14. Results of the U.S. Geological Survey's analytical evaluation program for standard reference samples distributed in October 1999

    USGS Publications Warehouse

    Farrar, T.W.

    2000-01-01

    This report presents the results of the U.S. Geological Survey's analytical evaluation program for six standard reference samples -- T-159 (trace constituents), M-152 (major constituents), N-63 (nutrient constituents), N-64 (nutrient constituents), P-33 (low ionic strength constituents), and Hg-29 (mercury) -- that were distributed in October 1999 to 149 laboratories enrolled in the U.S. Geological Survey sponsored interlaboratory testing program. Analytical data that were received from 131 of the laboratories were evaluated with respect to overall laboratory performance and relative laboratory performance for each analyte in the six reference samples. Results of these evaluations are presented in tabular form. Also presented are tables and graphs summarizing the analytical data provided by each laboratory for each analyte in the six standard reference samples. The most probable value for each analyte was determined using nonparametric statistics.

  15. Results of the U. S. Geological Survey's Analytical Evaluation Program for Standard Reference Samples Distributed in March 2002

    USGS Publications Warehouse

    Woodworth, M.T.; Conner, B.F.

    2002-01-01

    This report presents the results of the U.S. Geological Survey's analytical evaluation program for six standard reference samples -- T- 169 (trace constituents), M- 162 (major constituents), N-73 (nutrient constituents), N-74 (nutrient constituents), P-38 (low ionic-strength constituents), and Hg-34 (mercury) -- that were distributed in March 2002 to laboratories enrolled in the U.S. Geological Survey sponsored intedaboratory testing program. Analytical data received from 93 laboratories were evaluated with respect to overall laboratory performance and relative laboratory performance for each analyte in the six reference samples. Results of these evaluations are presented in tabular form. Also presented are tables and graphs summarizing the analytical data provided by each laboratory for each analyte in the six standard reference samples. The most probable value for each analyte was determined using nonparametric statistics.

  16. Assessment of Effectiveness of Geologic Isolation Systems: REFERENCE SITE INITIAL ASSESSMENT FOR A SALT DOME REPOSITORY

    SciTech Connect

    Harwell, M. A.; Brandstetter, A.; Benson, G. L.; Bradley, D. J.; Serne, R. J.; Soldat, J. K; Cole, C. R.; Deutsch, W. J.; Gupta, S. K.; Harwell, C. C.; Napier, B. A.; Reisenauer, A. E.; Prater, L. S.; Simmons, C. S.; Strenge, D. L.; Washburn, J. F.; Zellmer, J. T.

    1982-06-01

    As a methodology demonstration for the Office of Nuclear Waste Isolation (ONWI), the Assessment of Effectiveness of Geologic Isolation Systems (AEGIS) Program conducted an initial reference site analysis of the long-term effectiveness of a salt dome repository. The Hainesville Salt Dome in Texas was chosen to be representative of the Gulf Coast interior salt domes; however, the Hainesville Site has been eliminated as a possible nuclear waste repository site. The data used for this exercise are not adequate for an actual assessment, nor have all the parametric analyses been made that would adequately characterize the response of the geosystem surrounding the repository. Additionally, because this was the first exercise of the complete AEGIS and WASTE Rock Interaction Technology (WRIT) methodology, this report provides the initial opportunity for the methodology, specifically applied to a site, to be reviewed by the community outside the AEGIS. The scenario evaluation, as a part of the methodology demonstration, involved consideration of a large variety of potentially disruptive phenomena, which alone or in concert could lead to a breach in a salt dome repository and to a subsequent transport of the radionuclides to the environment. Without waste- and repository-induced effects, no plausible natural geologic events or processes which would compromise the repository integrity could be envisioned over the one-million-year time frame after closure. Near-field (waste- and repository-induced) effects were excluded from consideration in this analysis, but they can be added in future analyses when that methodology development is more complete. The potential for consequential human intrusion into salt domes within a million-year time frame led to the consideration of a solution mining intrusion scenario. The AEGIS staff developed a specific human intrusion scenario at 100 years and 1000 years post-closure, which is one of a whole suite of possible scenarios. This scenario

  17. Assessment of Effectiveness of Geologic Isolation Systems: REFERENCE SITE INITIAL ASSESSMENT FOR A SALT DOME REPOSITORY

    SciTech Connect

    Harwell, M. A.; Brandstetter, A.; Benson, G. L.; Raymond, J. R.; Brandley, D. J.; Serne, R. J.; Soldat, J. K.; Cole, C. R.; Deutsch, W. J.; Gupta, S. K.; Harwell, C. C.; Napier, B. A.; Reisenauer, A. E.; Prater, L. S.; Simmons, C. S.; Strenge, D. L.; Washburn, J. F.; Zellmer, J. T.

    1982-06-01

    As a methodology demonstration for the Office of Nuclear Waste Isolation (ONWI), the Assessment of Effectiveness of Geologic Isolation Systems (AEGIS) Program conducted an initial reference site analysis of the long-term effectiveness of a salt dome repository. The Hainesville Salt Dome in Texas was chosen to be representative of the Gulf Coast interior salt domes; however, the Hainesville Site has been eliminated as a possible nuclear waste repository site. The data used for this exercise are not adequate for an actual assessment, nor have all the parametric analyses been made that would adequately characterize the response of the geosystem surrounding the repository. Additionally, because this was the first exercise of the complete AEGIS and WASTE Rock Interaction Technology (WRIT) methodology, this report provides the initial opportunity for the methodology, specifically applied to a site, to be reviewed by the community outside the AEGIS. The scenario evaluation, as a part of the methodology demonstration, involved consideration of a large variety of potentially disruptive phenomena, which alone or in concert could lead to a breach in a salt dome repository and to a subsequent transport of the radionuclides to the environment. Without waste- and repository-induced effects, no plausible natural geologic events or processes which would compromise the repository integrity could be envisioned over the one-million-year time frame after closure. Near-field (waste- and repository-induced) effects were excluded from consideration in this analysis, but they can be added in future analyses when that methodology development is more complete. The potential for consequential human intrusion into salt domes within a million-year time frame led to the consideration of a solution mining intrusion scenario. The AEGIS staff developed a specific human intrusion scenario at 100 years and 1000 years post-closure, which is one of a whole suite of possible scenarios. This scenario

  18. Emission spectrographic determination of volatile trace elements in geologic materials by a carrier distillation technique

    USGS Publications Warehouse

    Barton, H.N.

    1986-01-01

    Trace levels of chalcophile elements that form volatile sulfide minerals are determined in stream sediments and in the nonmagnetic fraction of a heavy-mineral concentrate of stream sediments by a carrier distillation emission spectrographic method. Photographically recorded spectra of samples are visually compared with those of synthetic standards for the two sample types. Rock and soil samples may also be analyzed by comparison with the stream-sediment standards. A gallium oxide spectrochemical carrier/buffer enhances the early emission of the volatile elements. Detection limits in parts per million attained are: Sb 5, As 20, Bi 0.1, Cd 1, Cu 1, Pb 2, Ag 0.1, Zn 2, and Sn 0.1. A comparison with other methods of analysis, total-burn emission and atomic absorption spectroscopy, shows good correlation for standard reference for materials and samples from a variety of geologic terranes. ?? 1986.

  19. Aluminum analysis in biological reference material by nondestructive methods

    SciTech Connect

    Landsberger, S.; Arendt, A.; Keck, B.; Glascock, M.

    1988-01-01

    In recent years, the determination of aluminum in biological materials has become the subject of many research projects. This interest stems from an increasing knowledge of the toxicity of aluminum to both aquatic and human life. Unfortunately, the detection of aluminum in biological materials has proven troublesome. The use of traditional chemical determinations has been shown to be very long and somewhat complicated. Several attempts have been made using neutron activation analysis, but an interfering reaction must be taken into account. In this experiment the rabbit irradiation facilities at the University of Missouri Research Reactor were used. The aluminum concentrations for eight certified reference materials are shown. When US National Bureau of Standards (NBS) value is given as certified or as an information value, results agree very well. The results for NBS 1572 citrus leaves agree, and NBS 1577 results agree very well with that of Glascock et al.

  20. Material Spectral Emissivity Measurement Based on Two Reference Blackbodies

    NASA Astrophysics Data System (ADS)

    Cai, Jing; Yang, Yongjun; Liao, Li; Lyu, Guoyi

    2015-12-01

    Spectral emissivity is one of the important physical properties of materials. Emissivity measurement is critical for accurate temperature measurements and the evaluation of the stealth performance for materials. In this paper, a Fourier transform infrared spectrometer and an energy comparison method are used to study material emissivity measurements. Two reference blackbodies are employed for real-time measurement and correction of the spectrometer background function to enhance the emissivity measurement accuracy, to improve the design of a three-parabolic-mirror optical system, and to enlarge the optical field of view to meet the measurement requirements. The linearity of the system is measured using a mercury cadmium telluride detector and a deuterated triglycine sulfate detector. The results indicate that the linear range of the system meets the emissivity measurement requirements for the temperature range from 50°C to 1000° C. The effective radiation surface is introduced as a parameter of the reference blackbodies to reduce the influence of the measurement distance. The Fourier transform infrared spectrometer is used to measure the spectral emissivity of a conductive silica film and SiC, respectively, at different temperatures in the wavelength range of 1 \\upmu m to 25 \\upmu m. The expanded uncertainty is less than 5 %.

  1. Characterization of Ricin and R. communis Agglutinin Reference Materials.

    PubMed

    Worbs, Sylvia; Skiba, Martin; Söderström, Martin; Rapinoja, Marja-Leena; Zeleny, Reinhard; Russmann, Heiko; Schimmel, Heinz; Vanninen, Paula; Fredriksson, Sten-Åke; Dorner, Brigitte G

    2015-11-26

    Ricinus communis intoxications have been known for centuries and were attributed to the toxic protein ricin. Due to its toxicity, availability, ease of preparation, and the lack of medical countermeasures, ricin attracted interest as a potential biological warfare agent. While different technologies for ricin analysis have been established, hardly any universally agreed-upon "gold standards" are available. Expert laboratories currently use differently purified in-house materials, making any comparison of accuracy and sensitivity of different methods nearly impossible. Technically challenging is the discrimination of ricin from R. communis agglutinin (RCA120), a less toxic but highly homologous protein also contained in R. communis. Here, we established both highly pure ricin and RCA120 reference materials which were extensively characterized by gel electrophoresis, liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI MS/MS), and matrix-assisted laser desorption ionization-time of flight approaches as well as immunological and functional techniques. Purity reached >97% for ricin and >99% for RCA120. Different isoforms of ricin and RCA120 were identified unambiguously and distinguished by LC-ESI MS/MS. In terms of function, a real-time cytotoxicity assay showed that ricin is approximately 300-fold more toxic than RCA120. The highly pure ricin and RCA120 reference materials were used to conduct an international proficiency test.

  2. Characterization of Ricin and R. communis Agglutinin Reference Materials.

    PubMed

    Worbs, Sylvia; Skiba, Martin; Söderström, Martin; Rapinoja, Marja-Leena; Zeleny, Reinhard; Russmann, Heiko; Schimmel, Heinz; Vanninen, Paula; Fredriksson, Sten-Åke; Dorner, Brigitte G

    2015-12-01

    Ricinus communis intoxications have been known for centuries and were attributed to the toxic protein ricin. Due to its toxicity, availability, ease of preparation, and the lack of medical countermeasures, ricin attracted interest as a potential biological warfare agent. While different technologies for ricin analysis have been established, hardly any universally agreed-upon "gold standards" are available. Expert laboratories currently use differently purified in-house materials, making any comparison of accuracy and sensitivity of different methods nearly impossible. Technically challenging is the discrimination of ricin from R. communis agglutinin (RCA120), a less toxic but highly homologous protein also contained in R. communis. Here, we established both highly pure ricin and RCA120 reference materials which were extensively characterized by gel electrophoresis, liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI MS/MS), and matrix-assisted laser desorption ionization-time of flight approaches as well as immunological and functional techniques. Purity reached >97% for ricin and >99% for RCA120. Different isoforms of ricin and RCA120 were identified unambiguously and distinguished by LC-ESI MS/MS. In terms of function, a real-time cytotoxicity assay showed that ricin is approximately 300-fold more toxic than RCA120. The highly pure ricin and RCA120 reference materials were used to conduct an international proficiency test. PMID:26703723

  3. Characterization of Ricin and R. communis Agglutinin Reference Materials

    PubMed Central

    Worbs, Sylvia; Skiba, Martin; Söderström, Martin; Rapinoja, Marja-Leena; Zeleny, Reinhard; Russmann, Heiko; Schimmel, Heinz; Vanninen, Paula; Fredriksson, Sten-Åke; Dorner, Brigitte G.

    2015-01-01

    Ricinus communis intoxications have been known for centuries and were attributed to the toxic protein ricin. Due to its toxicity, availability, ease of preparation, and the lack of medical countermeasures, ricin attracted interest as a potential biological warfare agent. While different technologies for ricin analysis have been established, hardly any universally agreed-upon “gold standards” are available. Expert laboratories currently use differently purified in-house materials, making any comparison of accuracy and sensitivity of different methods nearly impossible. Technically challenging is the discrimination of ricin from R. communis agglutinin (RCA120), a less toxic but highly homologous protein also contained in R. communis. Here, we established both highly pure ricin and RCA120 reference materials which were extensively characterized by gel electrophoresis, liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI MS/MS), and matrix-assisted laser desorption ionization–time of flight approaches as well as immunological and functional techniques. Purity reached >97% for ricin and >99% for RCA120. Different isoforms of ricin and RCA120 were identified unambiguously and distinguished by LC-ESI MS/MS. In terms of function, a real-time cytotoxicity assay showed that ricin is approximately 300-fold more toxic than RCA120. The highly pure ricin and RCA120 reference materials were used to conduct an international proficiency test. PMID:26703723

  4. Nondestructive assay of fluorine in geological and other materials by instrumental photon activation analysis with a microtron

    NASA Astrophysics Data System (ADS)

    Krausová, Ivana; Mizera, Jiří; Řanda, Zdeněk; Chvátil, David; Krist, Pavel

    2015-01-01

    Reliable determination of low concentrations of fluorine in geological and coal samples is difficult. It usually requires tedious decomposition and dissolution of the sample followed by chemical conversion of fluorine into its anionic form. The present paper examines possibilities of non-destructive determination of fluorine, mainly in minerals, rocks and coal, by instrumental photon activation analysis (IPAA) using the MT-25 microtron. The fluorine assay consists of counting the positron-electron annihilation line of 18F at 511 keV, which is a product of the photonuclear reaction 19F(γ, n)18F and a pure positron emitter. The assay is complicated by the simultaneous formation of other positron emitters. The main contributors to interference in geological samples are from 45Ti and 34mCl, whereas those from 44Sc and 89Zr are minor. Optimizing beam energy and irradiation-decay-counting times, together with using interfering element calibration standards, allowed reliable IPAA determination of fluorine in selected USGS and CRPG geochemical reference materials, NIST coal reference materials, and NIST RM 8414 Bovine Muscle. In agreement with the published data obtained by PIGE, the results of the F assay by IPAA have revealed erroneous reference values provided for the NIST reference materials SRM 1632 Bituminous Coal and RM 8414 Bovine Muscle. The detection limits in rock and coal samples are in the range of 10-100 μg g-1.

  5. Molecularly uniform poly(ethylene glycol) certified reference material

    NASA Astrophysics Data System (ADS)

    Takahashi, Kayori; Matsuyama, Shigetomo; Kinugasa, Shinichi; Ehara, Kensei; Sakurai, Hiromu; Horikawa, Yoshiteru; Kitazawa, Hideaki; Bounoshita, Masao

    2015-02-01

    A certified reference material (CRM) for poly(ethylene glycol) with no distribution in the degree of polymerization was developed. The degree of polymerization of the CRM was accurately determined to be 23. Supercritical fluid chromatography (SFC) was used to separate the molecularly uniform polymer from a standard commercial sample with wide polydispersity in its degree of polymerization. Through the use of a specific fractionation system coupled with SFC, we are able to obtain samples of poly(ethylene glycol) oligomer with exact degrees of polymerization, as required for a CRM produced by the National Metrology Institute of Japan.

  6. Technologies for laboratory generation of dust from geological materials.

    PubMed

    Gill, Thomas E; Zobeck, Ted M; Stout, John E

    2006-04-30

    Dusts generated in the laboratory from soils and sediments are used to evaluate the emission intensities, composition, and environmental and health impacts of mineral aerosols. Laboratory dust generation is also utilized in other disciplines including process control and occupational hygiene in manufacturing, inhalation toxicology, environmental health and epidemiology, and pharmaceutics. Many widely available and/or easily obtainable laboratory or commercial appliances can be used to generate mineral aerosols, and several distinct classes of dust generators (fluidization devices, dustfall chambers, rotating drums/tubes) are used for geological particulate studies. Dozens of different devices designed to create dust from soils and sediments under controlled laboratory conditions are documented and described in this paper. When choosing a specific instrument, investigators must consider some important caveats: different classes of dust generators characterize different properties (complete collection of a small puff of aerosol versus sampling of a representative portion of a large aerosol cloud) and physical processes (resuspension of deposited dust versus in situ production of dust). The quantity "dustiness" has been used in industrial and environmental health research; though it has been quantified in different ways by different investigators, it should also be applicable to studies of geological aerosol production. Using standardized dust-production devices and definitions of dustiness will improve comparisons between laboratories and instruments: lessons learned from other disciplines can be used to improve laboratory research on the generation of atmospheric dusts from geological sources.

  7. Copper Oxide Precipitates in NBS Standard Reference Material 482

    PubMed Central

    Windsor, Eric S.; Carlton, Robert A.; Gillen, Greg; Wight, Scott A.; Bright, David S.

    2002-01-01

    Copper oxide has been detected in the copper containing alloys of NBS Standard Reference Material (SRM) 482. This occurrence is significant because it represents heterogeneity within a standard reference material that was certified to be homogeneous on a micrometer scale. Oxide occurs as elliptically to spherically shaped precipitates whose size differs with alloy composition. The largest precipitates occur in the Au20-Cu80 alloy and range in size from submicrometer up to 2 μm in diameter. Precipitates are observed using light microscopy, electron microscopy, and secondary ion mass spectrometry (SIMS). SIMS has demonstrated that the precipitates are present within all the SRM 482 wires that contain copper. Only the pure gold wire is precipitate free. Initial results from the analysis of the Au20-Cu80 alloy indicate that the percentage of precipitates is less than 1 % by area. Electron probe microanalysis (EPMA) of large (2 μm) precipitates in this same alloy indicates that precipitates are detectable by EPMA and that their composition differs significantly from the certified alloy composition. The small size and low percentage of these oxide precipitates minimizes the impact that they have upon the intended use of this standard for electron probe microanalysis. Heterogeneity caused by these oxide precipitates may however preclude the use of this standard for automated EPMA analyses and other microanalysis techniques. PMID:27446759

  8. Purity Determination of Acetaldehyde in an Acetaldehyde Certified Reference Material.

    PubMed

    Yamazaki, Taichi; Watanabe, Takuro; Nakamura, Satoe; Kato, Kenji

    2015-01-01

    Acetaldehyde is regulated as a toxic substance in various fields, and the method for monitoring or analysis of acetaldehyde is important. However, handling is difficult because of the high reactivity and low boiling point of acetaldehyde. Therefore, a reference material for high purity acetaldehyde with high accuracy was not available. Although the measuring method of acetaldehyde as a reagent is published in the Japanese Industrial Standard (JIS) where the specification of acetaldehyde purity is more than 80%, the analytical method described in JIS is not enough for an accuracy purity determination method. In this research, the high precision purity determination method for development of a certified reference material (CRM) of acetaldehyde was examined. By controlling the volatility and reactivity of acetaldehyde, we established the purity determination method of acetaldehyde with a relative standard uncertainty of less than 0.3%. Furthermore, this method was applied to develop a high purity acetaldehyde CRM with an expanded uncertainty of 0.005 kg kg(-1) (k = 2). PMID:26063006

  9. The new IAEA reference material: IAEA-434 technologically enhanced naturally occurring radioactive materials (TENORM) in phosphogypsum.

    PubMed

    Shakhashiro, A; Sansone, U; Wershofen, H; Bollhöfer, A; Kim, C K; Kim, C S; Kis-Benedek, G; Korun, M; Moune, M; Lee, S H; Tarjan, S; Al-Masri, M S

    2011-01-01

    A reliable determination of Technologically Enhanced Naturally Occurring Radioactive Materials in phosphogypsum is necessary to comply with radiation protection and environmental regulations. In this respect, a new phosphogypsum reference material was produced and certified to assist in the validation of analytical methods and the quality assurance of produced analytical results. This paper presents the sample preparation methodology, material homogeneity assessment, characterization campaign results and assignment of property values, and associated uncertainties. The reference values and associated uncertainties for Pb-210, Ra-226, Th-230, U-234 and U-238 were established based on consensus values calculated from analytical results reported by three National Metrology Institutes and five expert laboratories.

  10. Venera-Vega Geochemical Analyses: What Geologic Units are the Source of the Analyzed Material?

    NASA Astrophysics Data System (ADS)

    Abdrakhimov, A. M.; Basilevsky, A. T.

    2004-03-01

    Based on Basilevsky &Head (this conference), craters which ejecta contributed into the airfall deposits covered the Venera-Vega landing ellipses, were selected, then the contributions of deep-seated geologic units into the analyzed material were estimated.

  11. Development and characterisation of a new line width reference material

    NASA Astrophysics Data System (ADS)

    Dai, Gaoliang; Zhu, Fan; Heidelmann, Markus; Fritz, Georg; Bayer, Thomas; Kalt, Samuel; Fluegge, Jens

    2015-11-01

    A new critical dimension (CD, often synonymously used for line width) reference material with improved vertical parallel sidewalls (IVPSs) has been developed and characterised. The sample has a size of 6 mm  ×  6 mm, consisting of 4 groups of 5  ×  5 feature patterns. Each feature pattern has a group of five reference line features with a nominal CD of 50 nm, 70 nm, 90 nm, 110 nm and 130 nm, respectively. Each feature pattern includes a pair of triangular alignment marks, applicable for precisely identifying the target measurement position, e.g. for comparison or calibration between different tools. The geometry of line features has been investigated thoroughly using a high-resolution transmission electron microscope and a CD atomic force microscope (CD-AFM). Their results indicate the high quality of the line features: the top corner radius of  <7 nm, vertical sidewall (slope mostly within 90°  ±  0.5°) and very small line width variation (LWR down to 0.36 nm). The application of the developed sample for calibrating the scaling factor and effective tip geometry of the CD-AFM are demonstrated. The scaling factor of the CD-AFM is calibrated to be 0.9988, coinciding well with the theoretical value 1 as the tool was calibrated to a traceable metrological atomic force microscope. The effective width of a CDR120-EBD tip is calibrated as 128.32 nm. Finally, a strategy for the non-destructive calibration of the developed sample is introduced, which enables the application of the reference material in practice.

  12. Flouescence reference materials used for optical and biophotonic applications

    NASA Astrophysics Data System (ADS)

    Engel, A.; Otterman, C.; Klahn, J.; Enseling, D.; Korb, T.; Resch-Genger, U.; Hoffmann, K.; Schweizer, S.; Selling, J.; Kynast, U.; Koberling, F.; Rupertus, V.

    2007-07-01

    Fluorescence techniques are known for their high sensitivity and are widely used as analytical tools and detection methods for product and process control, material sciences, environmental and bio-technical analysis, molecular genetics, cell biology, medical diagnostics, and drug screening. According to DIN/ISO 17025 certified standards are used for fluorescence diagnostics having the drawback of giving relative values for fluorescence intensities only. Therefore reference materials for a quantitative characterization have to be related directly to the materials under investigation. In order to evaluate these figures it is necessary to calculate absolute numbers like absorption/excitation cross sections and quantum yield. This can be done for different types of dopands in different materials like glass, glass ceramics, crystals or nano crystalline material embedded in polymer matrices. Based on the optical spectroscopy data we will discuss options for characteristic doped glasses and glass ceramics with respect to scattering and absorption regime. It has shown recently for YAG:Ce glass ceramics that for a proper determination of the quantum efficiency in these highly scattering media a reference material with similar scattering and fluorescent properties is required. This may be performed using the emission decay measurement diagnostics, where the decay time is below 100 ns. In this paper we present first results of these aspects using well performing LUMOGEN RED organic pigments for a comparison of mainly transparent glass with glass ceramics doped with various amounts of dopands e.g. ions of raw earth elements and transition metals. The LUMOGEN red is embedded in silica and polyurethane matrices. Characterisations on wavelength accuracy and lifetime for different environmental conditions (temperature, UV irradiation) have been performed. Moreover intensity patterns and results for homogeneity, isotropy, photo and thermal stability will be discussed. In a next

  13. An ion-selective electrode method for determination of chlorine in geological materials

    USGS Publications Warehouse

    Aruscavage, P. J.; Campbell, E.Y.

    1983-01-01

    A method is presented for the determination of chlorine in geological materials, in which a chloride-selective ion electrode is used after decomposition of the sample with hydrofluoric acid and separation of chlorine in a gas-diffusion cell. Data are presented for 30 geological standard materials. The relative standard deviation of the method is estimated to be better than 8% for amounts of chloride of 10 ??g and greater. ?? 1983.

  14. The low-level radioactivity ocean sediment standard reference material

    SciTech Connect

    Inn, K.G.W.; Lin, Z.; Liggett, W.S.; Krey, P.W.

    1995-12-31

    Over the past decades, on the order of 10{sup 15} Becquerel nuclear waste have been stored in the oceans. Potential contamination of the oceans from leaking nuclear waste has caused world wide concern. Currently, early warning of ocean contamination near the waste dumping sites rely on monitoring systems being set up by different countries and agencies. Because the determination of low-level radioactivity in ocean sediment is a difficult technical task, a basis for measurement quality assurance, methods verification, and data comparability is needed. The recently certified NIST ocean sediment Standard Reference Material (SRM-4355) is a composite of 1% contaminated Irish Sea sediment and 99% of Chesapeake Bay sediment by weight. The sediments were blended, pulverized to a median particle size of 8 {mu}m, and reblended to achieve acceptable sample homogeneity. A statistical assessment of the intercomparison results from 19 laboratories has shown the material to be homogeneous down to 10 grams. The certified radionuclide concentration range from 0.4 to 230 mBq/g. A variety of radiochemical procedures and detection techniques have been used in the measurements to minimize possible systematic bias. Twelve radionuclides including {sup 40}K, {sup 90}Sr, {sup 137}Cs, {sup 226}Ra, {sup 228}Th, {sup 230}Th, {sup 232}Th, {sup 234}U, {sup 235}U, {sup 238}U, {sup 238}Pu, and {sup (239+240)}Pu were certified. The mean values were reported for an additional 10 uncertified radionuclides: {sup 129}I, {sup 155}Eu, {sup 210}Po, {sup 210}Pb, {sup 212}Pb, {sup 214}Pb, {sup 214}Bi, {sup 228}Ra, {sup 237}Np, and {sup 241}Am. The standard reference material in unit quantities of about 100 gram each will be available by the end of 1995.

  15. Analysis on the use of engineered barriers for geologic isolation of spent fuel in a reference salt site repository

    SciTech Connect

    Cloninger, M.O.; Cole, C.R.; Washburn, J.F.

    1980-12-01

    A perspective on the potential durability and effectiveness requirements for the waste form, container and other engineered barriers for geologic disposal of spent nuclear fuel has been developed. This perspective is based on calculated potential doses to individuals who may be exposed to radioactivity released from a repository via a groundwater transport pathway. These potential dose commitments were calculated with an integrated geosphere transport and bioshpere transport model. A sensitivity analysis was accomplished by varying four important system parameters, namely the waste radionuclide release rate from the repository, the delay prior to groundwater contact with the waste (leach initiation), aquifer flow velocity and flow path length. The nuclide retarding capacity of the geologic media, a major determinant of the isolation effectiveness, was not varied as a parameter but was held constant for a particular reference site. This analysis is limited to looking only at engineered barriers whose net effect is either to delay groundwater contact with the waste form or to limit the rate of release of radionuclides into the groundwater once contact has occurred. The analysis considers only leach incident scenarios, including a water well intrusion into the groundwater near a repository, but does not consider other human intrusion events or catastrophic events. The analysis has so far been applied to a reference salt site repository system and conclusions are presented.Basically, in nearly all cases, the regional geology is the most effective barrier to release of radionuclides to the biosphere; however, for long-lived isotopes of carbon, technetium and iodine, which were poorly sorbed on the geologic media, the geology is not very effective once a leach incident is initiated.

  16. Determination of Mercury in Aqueous and Geologic Materials by Continuous Flow-Cold Vapor-Atomic Fluorescence Spectrometry (CVAFS)

    USGS Publications Warehouse

    Hageman, Philip L.

    2007-01-01

    New methods for the determination of total mercury in geologic materials and dissolved mercury in aqueous samples have been developed that will replace the methods currently (2006) in use. The new methods eliminate the use of sodium dichromate (Na2Cr2O7 ?2H2O) as an oxidizer and preservative and significantly lower the detection limit for geologic and aqueous samples. The new methods also update instrumentation from the traditional use of cold vapor-atomic absorption spectrometry to cold vapor-atomic fluorescence spectrometry. At the same time, the new digestion procedures for geologic materials use the same size test tubes, and the same aluminum heating block and hot plate as required by the current methods. New procedures for collecting and processing of aqueous samples use the same procedures that are currently (2006) in use except that the samples are now preserved with concentrated hydrochloric acid/bromine monochloride instead of sodium dichromate/nitric acid. Both the 'old' and new methods have the same analyst productivity rates. These similarities should permit easy migration to the new methods. Analysis of geologic and aqueous reference standards using the new methods show that these procedures provide mercury recoveries that are as good as or better than the previously used methods.

  17. Characterization of Three Berry Standard Reference Materials for Nutrients

    PubMed Central

    Wood, Laura J.; Sharpless, Katherine E.; Pichon, Monique; Porter, Barbara J.; Yen, James H.; Ehling, Stefan

    2011-01-01

    The National Institute of Standards and Technology (NIST) has been working with the National Institutes of Health Office of Dietary Supplements to produce Standard Reference Materials (SRMs) of interest to analysts of dietary supplements. Some of these SRMs are traditional foods including SRM 3281 Cranberry (Fruit), SRM 3282 Low-Calorie Cranberry Juice Cocktail, and SRM 3287 Blueberry (Fruit), which have been characterized for nine nutritional elements and sugars. The blueberries have also been characterized for proximates, two water-soluble vitamins, and amino acids. These new materials are intended for use in method development and validation as well as for quality assurance and traceability when assigning values to in-house control materials. Foods can be difficult to analyze because of matrix effects. With the addition of these three new SRMs, it is now possible to more closely match controls to matrices and analyte levels for fruit and vegetable test samples. Several nutritional elements in these three SRMs are present at lower levels than those in other food-matrix SRMs. PMID:21688777

  18. A selected bibliography of references on geology, hydrology, and geochemistry of the Midwestern Basins and Arches region; Ohio, Indiana, Michigan, and Illinois

    USGS Publications Warehouse

    Robinson, Anthony; Bugliosi, Edward F.

    1994-01-01

    This report contains selected references used for the Midwestern Basins and Arches Regional Aquifer System Analysis project of the U.S. Geological Survey. The project was begun in 1988 to study the geologic framework, hydrology, and geochemistry of the surficial and the Silurian and Devonian carbonate-rock aquifers in the Midwestern Basins and Arches Region. The area of data collection is 90,000 square miles and includes parts of Ohio, Indiana, Michigan, and Illinois. Geologic, hydrologic, and geochemical references that apply to the hydrogeology and geochemistry of the region were collected and are presented in this bibliography by State and by geologic, hydrologic, and geochemical categories for each State.

  19. Bias detection and certified reference materials for random measurands

    NASA Astrophysics Data System (ADS)

    Rukhin, Andrew L.

    2015-12-01

    A problem that frequently occurs in metrology is the bias checking of data obtained by a laboratory against the specified value and uncertainty estimate given in the certificate of analysis. The measurand—a property of a certified reference material (CRM)—is supposed to be random with a normal distribution whose parameters are given by the certificate specifications. The laboratory’s data from subsequent measurements of the CRM (a CRM experiment) are summarized by the sample mean value and its uncertainty which is commonly based on a repeatability standard deviation. New confidence intervals for the lab’s bias are derived. Although they may lack intuitive appeal, those obtained by using higher order asymptotic methods, compared and contrasted in this paper, are recommended.

  20. Scalar material reference systems and loop quantum gravity

    NASA Astrophysics Data System (ADS)

    Giesel, K.; Thiemann, T.

    2015-07-01

    In the past, the possibility to employ (scalar) material reference systems in order to describe classical and quantum gravity directly in terms of gauge invariant (Dirac) observables has been emphasized frequently. This idea has been picked up more recently in loop quantum gravity with the aim to perform a reduced phase space quantization of the theory, thus possibly avoiding problems with the (Dirac) operator constraint quantization method for a constrained system. In this work, we review the models that have been studied on the classical and/or the quantum level and parametrize the space of theories considered so far. We then describe the quantum theory of a model that, to the best of our knowledge, has only been considered classically so far. This model could arguably be called the optimal one in this class of models considered as it displays the simplest possible true Hamiltonian, while at the same time reducing all constraints of general relativity.

  1. Certification of a new certified reference material of honokiol.

    PubMed

    Yang, Shiying; Yang, Dezhi; Hu, Kun; Zhou, Haohui; Guo, Yonghui; Du, Guanhua; Lu, Yang

    2015-07-01

    Honokiol is the most important active pharmaceutical ingredient in Magnolia officinalis, which is a famous traditional Chinese medicine and commonly used in clinical practice. In order to control the quality of honokiol and related pharmaceuticals, a new certified reference material (CRM) of honokiol was developed. The studies of sample preparation, homogeneity, stability, value assignment, and uncertainty evaluation were accomplished in this paper. Three different methods, including differential scanning calorimetry (DSC), mass balance method (MB), and coulometric titration (CT), were employed to determine the purity of honokiol. Specifically, the DSC and CT methods for purity determination of honokiol were established for the first time. The purity of honokiol CRM, after validation and evaluation, was found to be 99.3%, with an expanded uncertainty of 0.5% (k = 2).

  2. Production of Working Reference Materials for the Capability Evaluation Project

    SciTech Connect

    Phillip D. Noll, Jr.; Robert S. Marshall

    1999-03-01

    Nondestructive waste assay (NDA) methods are employed to determine the mass and activity of waste-entrained radionuclides as part of the National TRU (Trans-Uranic) Waste Characterization Program. In support of this program the Idaho National Engineering and Environmental Laboratory Mixed Waste Focus Area developed a plan to acquire capability/performance data on systems proposed for NDA purposes. The Capability Evaluation Project (CEP) was designed to evaluate the NDA systems of commercial contractors by subjecting all participants to identical tests involving 55 gallon drum surrogates containing known quantities and distributions of radioactive materials in the form of sealed-source standards, referred to as working reference materials (WRMs). Although numerous Pu WRMs already exist, the CEP WRM set allows for the evaluation of the capability and performance of systems with respect to waste types/configurations which contain increased amounts of {sup 241}Am relative to weapons grade Pu, waste that is dominantly {sup 241}Am, as well as wastes containing various proportions of depleted uranium. The CEP WRMs consist of a special mixture of PuO{sub 2}/AmO{sub 2} (IAP) and diatomaceous earth (DE) or depleted uranium (DU) oxide and DE and were fabricated at Los Alamos National Laboratory. The IAP WRMS are contained inside a pair of welded inner and outer stainless steel containers. The DU WRMs are singly contained within a stainless steel container equivalent to the outer container of the IAP standards. This report gives a general overview and discussion relating to the production and certification of the CEP WRMs.

  3. Mapping watershed potential to contribute phosphorus from geologic materials to receiving streams, southeastern United States

    USGS Publications Warehouse

    Terziotti, Silvia; Hoos, Anne B.; Harned, Douglas; Garcia, Ana Maria

    2010-01-01

    As part of the southeastern United States SPARROW (SPAtially Referenced Regressions On Watershed attributes) water-quality model implementation, the U.S. Geological Survey created a dataset to characterize the contribution of phosphorus to streams from weathering and erosion of surficial geologic materials. SPARROW provides estimates of total nitrogen and phosphorus loads in surface waters from point and nonpoint sources. The characterization of the contribution of phosphorus from geologic materials is important to help separate the effects of natural or background sources of phosphorus from anthropogenic sources of phosphorus, such as municipal wastewater or agricultural practices. The potential of a watershed to contribute phosphorus from naturally occurring geologic materials to streams was characterized by using geochemical data from bed-sediment samples collected from first-order streams in relatively undisturbed watersheds as part of the multiyear U.S. Geological Survey National Geochemical Survey. The spatial pattern of bed-sediment phosphorus concentration is offered as a tool to represent the best available information at the regional scale. One issue may weaken the use of bed-sediment phosphorus concentration as a surrogate for the potential for geologic materials in the watershed to contribute to instream levels of phosphorus-an unknown part of the variability in bed-sediment phosphorus concentration may be due to the rates of net deposition and processing of phosphorus in the streambed rather than to variability in the potential of the watershed's geologic materials to contribute phosphorus to the stream. Two additional datasets were created to represent the potential of a watershed to contribute phosphorus from geologic materials disturbed by mining activities from active mines and

  4. Simulation of Shock Loading in Saturated Geologic Materials

    SciTech Connect

    Liu, B T; Lomov, I; Vorobiev, O

    2004-09-17

    The effective stress model is used to model the stress-strain, volumetric, and strength behavior in saturated materials under shock loading. The effective stress concept provides a predictive model of the behavior of wet porous materials based on the dry material properties. An effective stress model that allows for arbitrary fluid and solid equations of state and varying levels of saturation is incorporated into an adaptive mesh refinement (AMR) Eulerian shock physics hydrocode. Good agreement is found between simulation results and experimental data for saturated materials, even at moderately high pressures.

  5. Determination of mercury in geological materials by continuous-flow, cold-vapor, atomic absorption spectrophotometry

    SciTech Connect

    Kennedy, K.R.; Crock, J.G.

    1987-06-01

    To determine mercury in geological materials, samples are digested with nitric acid and sodium dichromate in a closed teflon vessel. After bringing to a constant weight, the digest is mixed with air and a sodium chloride-hydroxylamine hydrochloride-sulfuric acid solution and then Hg(II) is reduced to Hg/sup 0/ with stannous chloride in a continuous flow manifold. The mercury vapor is then separated and measured using cold vapor atomic absorption spectrophotometry (CV-AAS). For a 100 mg sample the limit of detection is 20 parts-per-billion (ppb) Hg in sample. To obtain a 1% absorption signal, the described method requires 0.21 ppb Hg solution (equal to 16 ppb in sample). Precision is acceptable at less than 1.2% RSD for a 10 ppb Hg aqueous standard. Accuracy is demonstrated by the results of the analysis on standard reference materials. Several elements do interfere but the effect is minimal because either the digestion procedure does not dissolve them (e.g., Au or Pt) or they are normally of low abundance (e.g., Se or Te).

  6. Medical geology in tropical countries with special reference to Sri Lanka.

    PubMed

    Dissanayake, C B; Chandrajith, Rohana

    2007-04-01

    Sri Lanka provides an ideal opportunity for the study of the effect of geology on human health. The vast majority of the people of Sri Lanka still live in rural areas within areas termed geochemical provinces. Very broadly, one could say that a geochemical province has characteristic chemical composition in soil, water stream sediments and rocks, enabling their delineation from others. The chemical composition is presumed to be have an impact on the health of the inhabitants of the particular geochemical province, particularly because of the fact that their food and water are obtained mostly from the terrain itself. This leads to the concept of "diseases of geochemical origin". Among these are dental fluorosis, iodine deficiency disorders (IDDs) and selenium-based diseases. The Dry Zone of Sri Lanka has several areas rich in groundwater fluoride, the ingestion of which leads to dental fluorosis. Iodine deficiency diseases are more common in the Wet Zone, though their aetiologies are more complicated. Interestingly, it has also been observed that significant proportions of the female population of Sri Lanka are selenium-deficient, which could well be related to the geological environment. Chronic renal failure (CRF) has been observed in some areas of the Dry Zone of Sri Lanka, where there is a relationship of CRF with the mineral content of drinking water. This subject matter falls under the auspices of Medical Geology, a scientific discipline still in its infancy, and much more concerted studies are needed to attract the attention of medical research.

  7. Anorganic fluorescence reference materials for decay time of fluorescence emission

    NASA Astrophysics Data System (ADS)

    Engel, A.; Ottermann, C.; Klahn, J.; Korb, T.; Resch-Genger, U.; Hoffmann, K.; Kynast, U.; Rupertus, V.

    2008-02-01

    Fluorescence techniques are known for their high sensitivity and are widely used as analytical tools, detection methods and imaging applications for product and process control, material sciences, environmental and bio-technical analysis, molecular genetics, cell biology, medical diagnostics, and drug screening. According to DIN/ISO 17025 certified standards are used for steady state fluorescence diagnostics, a method having the drawback of giving relative values for fluorescence intensities only. Therefore reference materials for a quantitative characterization have to be related directly to the materials under investigation. In order to evaluate these figures it is necessary to calculate absolute numbers such as absorption/excitation cross sections and quantum yield. This has been done for different types of dopands in different materials such as glass, glass ceramics, crystals or nano crystalline material embedded in polymer matrices. Samples doped with several fluophores of different emission wavelengths and decay times are required for fluorescent multiplexing applications. Decay times shorter than 100 ns are of special interest. In addition, a proper knowledge is necessary of quantum efficiency in highly scattering media. Recently, quantum efficiency in YAG:Ce glass ceramics has been successfully investigated. Glass and glass ceramics doped with threefold charged rare earth elements are available. However, these samples have the disadvantage of emission decay times much longer than 1 microsecond, due to the excitation and emission of their optical forbidden electronic transitions. Therefore first attempts have been made to produce decay-time standards based on organic and inorganic fluophores. Stable LUMOGEN RED pigments and YAG:Ce phosphors are diluted simultaneously in silicone matrices using a wide range of concentrations between 0.0001 and 2 wt%. Organic LUMOGEN RED has decay times in the lower nanosecond range with a slight dependency on concentration

  8. Processing of Neutron Diffraction Data for Strain Measurement in Geological Materials

    SciTech Connect

    Polsky, Yarom; An, Ke; Anovitz, Lawrence {Larry} M; Bingham, Philip R; Carmichael, Justin R; Dessieux Jr, Luc Lucius

    2014-01-01

    : Conventional rock mechanics testing techniques typically involve the loading of samples and measurement of displacements or strains on the outer boundary of the specimen surface. Neutron diffraction based strain measurement techniques represent a unique and powerful tool for measuring the strain within geological materials under load. The structural variability and non-uniform crystallinity of geological materials, however, create many complexities in the intensity patterns that must be analyzed to quantify strains within the material. The attenuating and scattering properties of the pressure cell housing the sample further add difficulties to the data analysis. This paper describes the methods and processes used to process neutron scattering data for strain measurement in geological materials. It is intended to provide a primer for those in the rock mechanics community that are interested in utilizing this technique along with additional discussion of neutron diffraction experimental factors that may affect data quality.

  9. Precise Measurement of Stable Neodymium Isotopes of Geological Materials by Using MC-ICP-MS

    NASA Astrophysics Data System (ADS)

    Ma, J.; Wei, G.; Liu, Y.; Ren, Z.; Xu, Y.

    2013-12-01

    A method has developed to determine high-precision high precision stable Nd isotopes in geological materials by multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) using sample-standard-bracketing (SSB) mode. Nd was pre-concentrated and purifed and through a two column ion-exchange chromatographic procedure, yeilding a recovery of >96% for Nd with the interferences such as Ce and Sm being removed to cause little influence on the stable Nd isotopic compositions. The internal precision for the stable Nd isotopic compositions, ɛ142Nd, ɛ145Nd, ɛ146Nd and ɛ148Nd were generally better than ×0.2 (2SEM: standard error of the mean), and the external precision were generally better than ×0.2 (1SD: standard deviation) for ɛ142Nd, ɛ145Nd and ɛ146Nd, and better than ×0.5 (1SD) for ɛ148Nd estimated by the long-term results of the Nd standard solutions, such as La Jolla, Nd-GIG and NIST 3135a. Such precision id comparable to those by double spike method. Our measured ɛ142Nd, ɛ145Nd, ɛ146Nd and ɛ148Nd results of La Jolla are indentical to those by double spike method winthin analytical error. Thus, our method can provide comparable results for stable Nd isotopes to those by double spike method, but free from the inconvenience of calibrationg double spikes. This provides a more convenient means for studying stabe Nd isotopes in geological processes. By using this method, the stable Nd isotopic compositions for a series of international rock standard references were measured.

  10. Science Reference Materials for Children and Young Adults

    ERIC Educational Resources Information Center

    Strickler, Richard L.

    1974-01-01

    After a brief discussion of science reference service, there is a list of science reference books. First are general science books, then specific lists by broad Dewey decimal classes. Grade levels are given for each work. (LS)

  11. Development of reference conditions for geologic repositories for nuclear waste in the USA

    SciTech Connect

    Raines, G. E.; Rickertsen, L. D.; Claiborne, H. C.; McElroy, J. L.; Lynch, R. W.

    1980-10-01

    Activities to determine interim reference conditions for temperatures, pressure, fluid, chemical, and radiation environments that are expected to exist in commercial and defense high-level nuclear waste and spent fuel repositories in salt, basalt, tuff, granite, and shale are summarized. These interim conditions are being generated by the Reference Repository Conditions Interface Working Groups (RRC-IWG), an ad hoc IWG established by the National Waste Terminal Storage Program's (NWTS) Isolation Interface Control Board (I-ICB).

  12. Development of working reference materials for clinical virology.

    PubMed

    Fryer, Jacqueline F; Baylis, Sally A; Gottlieb, Anna L; Ferguson, Morag; Vincini, Giuseppe A; Bevan, Valerie M; Carman, William F; Minor, Philip D

    2008-12-01

    Nucleic acid amplification technique (NAT)-based assays are replacing traditional diagnostic methods in clinical laboratories. However, many of these assays are developed in-house and the lack of standardised reference materials has hindered assay implementation and control. Consequently, in the UK, the Clinical Virology Network (CVN), the National Institute for Biological Standards and Control (NIBSC), and the Health Protection Agency (HPA), are working in collaboration to develop working standards or 'run controls' for diagnostic NAT-based assays, particularly real-time PCR. These run controls are intended for use in microbiology laboratories and are designed to be extracted and amplified in the same way as clinical samples and included in each assay run. The aim is to enable clinical laboratories to continuously monitor the performance of their diagnostic NAT assays on a run-by-run basis allowing inter-laboratory comparisons, and ultimately improving the consistency of results. At present, eight candidate run controls representing clinically relevant viral targets have been prepared for evaluation by CVN laboratories. Data have been returned on the performance of each run control in routine diagnostic assays. Preliminary results presented here indicate a high level of variability in intra- and inter-assay detection of these targets, highlighting the need for standardisation of assays within molecular diagnostics.

  13. Mica Mountain Muscovite: A New Silicate Hydrogen Isotope Standard Reference Material

    NASA Astrophysics Data System (ADS)

    Lonero, A.; Larson, P. B.; Neill, O. K.

    2015-12-01

    A new standard reference material consisting of finely ground muscovite flakes has been developed and utilized at Washington State University to calibrate hydrogen isotope ratio (D/H) measurements to the VSMOW scale. This standard was prepared from a single crystal 'book' of a muscovite-bearing pegmatite near Deary, ID. The value we obtained for this muscovite standard (MMM) is: δD VSMOW = -79.1 ± 2.0‰ relative to NBS-30 biotite at -65.7‰ compared to a VSMOW value of 0.00‰. This mean value was determined for the muscovite and has been used as our working standard. There have been many recent geological applications to continuous flow isotope ratio mass spectroscopy. When hydrogen isotope ratios are of interest, a suitable standard for hydrogen in silicate systems often is not available. With supplies of the older NBS-30 biotite standard exhausted, much D/H data measured on silicate minerals have been linked to the VSMOW scale via non-silicate reference materials which may not behave similarly to minerals under study. Some recent studies have shown the NBS-30 standard to have poor intra-laboratory agreement with that material's measured and accepted isotopic values (Qi et al., 2014). Many laboratories which would measure D/H in silicate minerals would benefit from using a silicate-based standard for hydrogen. With further characterization, this muscovite may also be useful as a standard for silicate oxygen ratios as well as for some major element cations. This muscovite standard gives consistent values and it is easy to work with and does not leave much combustion residue. Also, because muscovite contains little iron, metal-hydride formation and associated fractionation factors is greatly reduced during the sample combustion. A new silicate-hydrogen standard is needed by the community, and this work represents an example of what a replacement standard material could look like.

  14. SIMULATION OF SHOCK WAVE PROPAGATION AND DAMAGE IN GEOLOGIC MATERIALS

    SciTech Connect

    Lomov, I; Vorobiev, O; Antoun, T H

    2004-09-17

    A new thermodynamically consistent material model for large deformation has been developed. It describes quasistatic loading of limestone as well as high-rate phenomena. This constitutive model has been implemented into an Eulerian shock wave code with adaptive mesh refinement. This approach was successfully used to reproduce static triaxial compression tests and to simulate experiments of blast loading and damage of limestone. Results compare favorably with experimentally available wave profiles from spherically-symmetric explosion in rock samples.

  15. Standard Reference Material (SRM 1990) For Single Crystal Diffractometer Alignment

    PubMed Central

    Wong-Ng, W.; Siegrist, T.; DeTitta, G. T.; Finger, L. W.; Evans, H. T.; Gabe, E. J.; Enright, G. D.; Armstrong, J. T.; Levenson, M.; Cook, L. P.; Hubbard, C. R.

    2001-01-01

    An international project was successfully completed which involved two major undertakings: (1) a round-robin to demonstrate the viability of the selected standard and (2) the certification of the lattice parameters of the SRM 1990, a Standard Reference Material® for single crystal diffractometer alignment. This SRM is a set of ≈3500 units of Cr-doped Al2O3, or ruby spheres [(0.420.011 mole fraction % Cr (expanded uncertainty)]. The round-robin consisted of determination of lattice parameters of a pair of crystals: the ruby sphere as a standard, and a zeolite reference to serve as an unknown. Fifty pairs of crystals were dispatched from Hauptman-Woodward Medical Research Institute to volunteers in x-ray laboratories world-wide. A total of 45 sets of data was received from 32 laboratories. The mean unit cell parameters of the ruby spheres was found to be a=4.7608 ű0.0062 Å, and c=12.9979 ű0.020 Å (95 % intervals of the laboratory means). The source of errors of outlier data was identified. The SRM project involved the certification of lattice parameters using four well-aligned single crystal diffractometers at (Bell Laboratories) Lucent Technologies and at NRC of Canada (39 ruby spheres), the quantification of the Cr content using a combined microprobe and SEM/EDS technique, and the evaluation of the mosaicity of the ruby spheres using a double-crystal spectrometry method. A confirmation of the lattice parameters was also conducted using a Guinier-Hägg camera. Systematic corrections of thermal expansion and refraction corrections were applied. These rubies– are rhombohedral, with space group R3¯c. The certified mean unit cell parameters are a=4.76080±0.00029 Å, and c=12.99568 ű0.00087 Å (expanded uncertainty). These certified lattice parameters fall well within the results of those obtained from the international round-robin study. The Guinier-Hägg transmission measurements on five samples of powdered rubies (a=4.7610 ű0.0013 Å, and c = 12

  16. Standard Reference Material (SRM 1990) For Single Crystal Diffractometer Alignment.

    PubMed

    Wong-Ng, W; Siegrist, T; DeTitta, G T; Finger, L W; Evans, H T; Gabe, E J; Enright, G D; Armstrong, J T; Levenson, M; Cook, L P; Hubbard, C R

    2001-01-01

    An international project was successfully completed which involved two major undertakings: (1) a round-robin to demonstrate the viability of the selected standard and (2) the certification of the lattice parameters of the SRM 1990, a Standard Reference Material(®) for single crystal diffractometer alignment. This SRM is a set of ≈3500 units of Cr-doped Al2O3, or ruby spheres [(0.420.011 mole fraction % Cr (expanded uncertainty)]. The round-robin consisted of determination of lattice parameters of a pair of crystals: the ruby sphere as a standard, and a zeolite reference to serve as an unknown. Fifty pairs of crystals were dispatched from Hauptman-Woodward Medical Research Institute to volunteers in x-ray laboratories world-wide. A total of 45 sets of data was received from 32 laboratories. The mean unit cell parameters of the ruby spheres was found to be a=4.7608 ű0.0062 Å, and c=12.9979 ű0.020 Å (95 % intervals of the laboratory means). The source of errors of outlier data was identified. The SRM project involved the certification of lattice parameters using four well-aligned single crystal diffractometers at (Bell Laboratories) Lucent Technologies and at NRC of Canada (39 ruby spheres), the quantification of the Cr content using a combined microprobe and SEM/EDS technique, and the evaluation of the mosaicity of the ruby spheres using a double-crystal spectrometry method. A confirmation of the lattice parameters was also conducted using a Guinier-Hägg camera. Systematic corrections of thermal expansion and refraction corrections were applied. These rubies- are rhombohedral, with space group [Formula: see text]. The certified mean unit cell parameters are a=4.76080±0.00029 Å, and c=12.99568 ű0.00087 Å (expanded uncertainty). These certified lattice parameters fall well within the results of those obtained from the international round-robin study. The Guinier-Hägg transmission measurements on five samples of powdered rubies (a=4.7610 ű0.0013

  17. Standard Reference Material (SRM 1990) For Single Crystal Diffractometer Alignment.

    PubMed

    Wong-Ng, W; Siegrist, T; DeTitta, G T; Finger, L W; Evans, H T; Gabe, E J; Enright, G D; Armstrong, J T; Levenson, M; Cook, L P; Hubbard, C R

    2001-01-01

    An international project was successfully completed which involved two major undertakings: (1) a round-robin to demonstrate the viability of the selected standard and (2) the certification of the lattice parameters of the SRM 1990, a Standard Reference Material(®) for single crystal diffractometer alignment. This SRM is a set of ≈3500 units of Cr-doped Al2O3, or ruby spheres [(0.420.011 mole fraction % Cr (expanded uncertainty)]. The round-robin consisted of determination of lattice parameters of a pair of crystals: the ruby sphere as a standard, and a zeolite reference to serve as an unknown. Fifty pairs of crystals were dispatched from Hauptman-Woodward Medical Research Institute to volunteers in x-ray laboratories world-wide. A total of 45 sets of data was received from 32 laboratories. The mean unit cell parameters of the ruby spheres was found to be a=4.7608 ű0.0062 Å, and c=12.9979 ű0.020 Å (95 % intervals of the laboratory means). The source of errors of outlier data was identified. The SRM project involved the certification of lattice parameters using four well-aligned single crystal diffractometers at (Bell Laboratories) Lucent Technologies and at NRC of Canada (39 ruby spheres), the quantification of the Cr content using a combined microprobe and SEM/EDS technique, and the evaluation of the mosaicity of the ruby spheres using a double-crystal spectrometry method. A confirmation of the lattice parameters was also conducted using a Guinier-Hägg camera. Systematic corrections of thermal expansion and refraction corrections were applied. These rubies- are rhombohedral, with space group [Formula: see text]. The certified mean unit cell parameters are a=4.76080±0.00029 Å, and c=12.99568 ű0.00087 Å (expanded uncertainty). These certified lattice parameters fall well within the results of those obtained from the international round-robin study. The Guinier-Hägg transmission measurements on five samples of powdered rubies (a=4.7610 ű0.0013

  18. Standard Reference Material (SRM 1990) for Single Crystal Diffractometer Alignment

    USGS Publications Warehouse

    Wong-Ng, W.; Siegrist, T.; DeTitta, G.T.; Finger, L.W.; Evans, H.T.; Gabe, E.J.; Enright, G.D.; Armstrong, J.T.; Levenson, M.; Cook, L.P.; Hubbard, C.R.

    2001-01-01

    An international project was successfully completed which involved two major undertakings: (1) a round-robin to demonstrate the viability of the selected standard and (2) the certification of the lattice parameters of the SRM 1990, a Standard Reference Material?? for single crystal diffractometer alignment. This SRM is a set of ???3500 units of Cr-doped Al2O3, or ruby spheres [(0 420.011 mole fraction % Cr (expanded uncertainty)]. The round-robin consisted of determination of lattice parameters of a pair of crystals' the ruby sphere as a standard, and a zeolite reference to serve as an unknown. Fifty pairs of crystals were dispatched from Hauptman-Woodward Medical Research Institute to volunteers in x-ray laboratories world-wide. A total of 45 sets of data was received from 32 laboratories. The mean unit cell parameters of the ruby spheres was found to be a=4.7608 A?? ?? 0.0062 A??, and c=12.9979 A?? ?? 0.020 A?? (95 % intervals of the laboratory means). The source of errors of outlier data was identified. The SRM project involved the certification of lattice parameters using four well-aligned single crystal diffractometers at (Bell Laboratories) Lucent Technologies and at NRC of Canada (39 ruby spheres), the quantification of the Cr content using a combined microprobe and SEM/EDS technique, and the evaluation of the mosaicity of the ruby spheres using a double-crystal spectrometry method. A confirmation of the lattice parameters was also conducted using a Guinier-Ha??gg camera. Systematic corrections of thermal expansion and refraction corrections were applied. These rubies_ are rhombohedral, with space group R3c. The certified mean unit cell parameters are a=4.76080 ?? 0.00029 A??, and c=12 99568 A?? ?? 0.00087 A?? (expanded uncertainty). These certified lattice parameters fall well within the results of those obtained from the international round-robin study. The Guinier-Ha??gg transmission measurements on five samples of powdered rubies (a=4.7610 A?? ?? 0

  19. Development of a multi-VOC reference material for quality assurance in materials emission testing.

    PubMed

    Nohr, Michael; Horn, Wolfgang; Jann, Oliver; Richter, Matthias; Lorenz, Wilhelm

    2015-04-01

    Emission test chamber measurement is necessary to proof building materials as sources of volatile organic compounds (VOCs). The results of such measurements are used to evaluate materials and label them according to their potential to emit harmful substances, polluting indoor air. If only labelled materials were installed indoors, this would improve indoor air quality and prevent negative impacts on human health. Because of the complex testing procedure, reference materials for the quality assurance are mandatory. Currently, there is a lack of such materials because most building products show a broad variation of emissions even within one batch. A previous study indicates lacquers, mixed with volatile organic pollutants, as reproducible emission source for a wide range of substances. In the present study, the curing of the lacquer-VOC mixture inside micro-chambers was optimised. Therefore, the humidity and the chamber flow were varied. Typical indoor air pollutants with a wide range of volatilities, for example, styrene, n-hexadecane, dimethyl and dibutyl phthalate were selected. It turned out that, under optimised curing parameters inside the micro-chamber, their emission can be reproduced with variations of less than 10 %. With this, a next important step towards a reference material for emission testing was achieved. PMID:25543146

  20. Development of a multi-VOC reference material for quality assurance in materials emission testing.

    PubMed

    Nohr, Michael; Horn, Wolfgang; Jann, Oliver; Richter, Matthias; Lorenz, Wilhelm

    2015-04-01

    Emission test chamber measurement is necessary to proof building materials as sources of volatile organic compounds (VOCs). The results of such measurements are used to evaluate materials and label them according to their potential to emit harmful substances, polluting indoor air. If only labelled materials were installed indoors, this would improve indoor air quality and prevent negative impacts on human health. Because of the complex testing procedure, reference materials for the quality assurance are mandatory. Currently, there is a lack of such materials because most building products show a broad variation of emissions even within one batch. A previous study indicates lacquers, mixed with volatile organic pollutants, as reproducible emission source for a wide range of substances. In the present study, the curing of the lacquer-VOC mixture inside micro-chambers was optimised. Therefore, the humidity and the chamber flow were varied. Typical indoor air pollutants with a wide range of volatilities, for example, styrene, n-hexadecane, dimethyl and dibutyl phthalate were selected. It turned out that, under optimised curing parameters inside the micro-chamber, their emission can be reproduced with variations of less than 10 %. With this, a next important step towards a reference material for emission testing was achieved.

  1. Bottom-up effects of geologic parent material through ecological interaction webs

    NASA Astrophysics Data System (ADS)

    Bradley, R.

    2012-04-01

    Community ecologists study the interactions between species to understand what controls the distribution and abundance of different populations. Communities are thus portrayed as "interaction webs", in which different species exert reciprocal pressures on each other. In the case of one population being a resource for which another population is the consumer (i.e. food-web), reciprocal pressures are commonly referred to as "bottom-up" vs. "top-down" effects. The starting point for studying bottom-up effects is usually the vegetation (primary producers), and its end-point the decomposer community responsible for breaking down detrital matter from each trophic level. In my presentation, I will present results from three former graduate students, to argue that the starting point for studying bottom-up effects should be the geologic parent material (GPM), whose importance has often been overlooked by community ecologists. For example, our data show that GPM had a stronger effect on forest floor nutrient budgets than the identity or successional stage of the vegetation. Likewise, GPM had a strong effect on the structure of forest floor microbial communities, as well as their resistance to, and resilience from, disturbance. GPM also had a significant effect on the richness and diversity of understory plant communities from similar forest stands. Finally, we present evidence that soil fertility controls the resistance and tolerance of certain plant species to selective browsing, thereby affecting the composition of the dominant plant cover and the feeding patterns of large herbivores.

  2. Development of a Northern Continental Air Standard Reference Material.

    PubMed

    Rhoderick, George C; Kitzis, Duane R; Kelley, Michael E; Miller, Walter R; Hall, Bradley D; Dlugokencky, Edward J; Tans, Pieter P; Possolo, Antonio; Carney, Jennifer

    2016-03-15

    The National Institute of Standards and Technology (NIST) recently began to develop standard mixtures of greenhouse gases as part of a broad program mandated by the 2009 United States Congress to support research in climate change. To this end, NIST developed suites of gravimetrically assigned primary standard mixtures (PSMs) comprising carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) in a dry-natural air balance at ambient mole fraction levels. In parallel, the National Oceanic and Atmospheric Administration (NOAA) in Boulder, Colorado, charged 30 aluminum gas cylinders with northern hemisphere air at Niwot Ridge, Colorado. These mixtures, which constitute NIST Standard Reference Material (SRM) 1720 Northern Continental Air, were certified by NIST for ambient mole fractions of CO2, CH4, and N2O relative to NIST PSMs. NOAA-assigned values are also provided as information in support of the World Meteorological Organization (WMO) Global Atmosphere Watch (GAW) Program for CO2, CH4, and N2O, since NOAA serves as the WMO Central Calibration Laboratory (CCL) for CO2, CH4, and N2O. Relative expanded uncertainties at the 95% confidence interval are <±0.06% of the certified values for CO2 and N2O and <0.2% for CH4, which represents the smallest relative uncertainties specified to date for a gaseous SRM produced by NIST. Agreement between the NOAA (WMO/GAW) and NIST values based on their respective calibration standards suites is within 0.05%, 0.13%, and 0.06% for CO2, CH4, and N2O, respectively. This collaborative development effort also represents the first of its kind for a gaseous SRM developed by NIST. PMID:26890890

  3. Development of a Northern Continental Air Standard Reference Material.

    PubMed

    Rhoderick, George C; Kitzis, Duane R; Kelley, Michael E; Miller, Walter R; Hall, Bradley D; Dlugokencky, Edward J; Tans, Pieter P; Possolo, Antonio; Carney, Jennifer

    2016-03-15

    The National Institute of Standards and Technology (NIST) recently began to develop standard mixtures of greenhouse gases as part of a broad program mandated by the 2009 United States Congress to support research in climate change. To this end, NIST developed suites of gravimetrically assigned primary standard mixtures (PSMs) comprising carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) in a dry-natural air balance at ambient mole fraction levels. In parallel, the National Oceanic and Atmospheric Administration (NOAA) in Boulder, Colorado, charged 30 aluminum gas cylinders with northern hemisphere air at Niwot Ridge, Colorado. These mixtures, which constitute NIST Standard Reference Material (SRM) 1720 Northern Continental Air, were certified by NIST for ambient mole fractions of CO2, CH4, and N2O relative to NIST PSMs. NOAA-assigned values are also provided as information in support of the World Meteorological Organization (WMO) Global Atmosphere Watch (GAW) Program for CO2, CH4, and N2O, since NOAA serves as the WMO Central Calibration Laboratory (CCL) for CO2, CH4, and N2O. Relative expanded uncertainties at the 95% confidence interval are <±0.06% of the certified values for CO2 and N2O and <0.2% for CH4, which represents the smallest relative uncertainties specified to date for a gaseous SRM produced by NIST. Agreement between the NOAA (WMO/GAW) and NIST values based on their respective calibration standards suites is within 0.05%, 0.13%, and 0.06% for CO2, CH4, and N2O, respectively. This collaborative development effort also represents the first of its kind for a gaseous SRM developed by NIST.

  4. Asbestos as reference material for fibre-induced cancer.

    PubMed

    Muhle, H; Pott, F

    2000-06-01

    The objective of this paper is to review published data on the carcinogenicity of asbestos fibres with regard to the elucidation of a potential risk originating from exposure to man-made vitreous fibres (MMVF). Steps in the comparison of the two fibre classes are characterization of the fibres, pulmonary deposition, biodurability and biopersistence and a review of the cancer risk from asbestos fibres after inhalation in rats and humans. Various dust samples of chrysotile, crocidolite, and amosite were used as reference materials in studies with experimental animals. These fibres are normally thinner and shorter than MMVF. These differences in dimensions cause differences in the deposition in the airways. In addition, significant dissimilarities exist in the deposition pattern between rats and humans. Data from biopersistence studies show that focusing only on fibres longer than 20 microm and using weighted half-time for a characterization of risk may be misleading. Inhalation experiments with rats need fibre exposure concentrations over 100 times higher to match the lung cancer risk of asbestos workers, and about 1,000 times higher to reach the same mesothelioma risk. Also, the striking difference between the low lung burden of amphibole fibres of asbestos workers with mesothelioma and the more than 1,000 times higher lung burden of rats with a low mesothelioma risk demonstrates the low sensitivity of the inhalation test model for the carcinogenic potency even of crocidolite fibres. It can be concluded that the rat inhalation model is also not sensitive enough to predict the cancer risk of other fibre types for humans.

  5. New Ca-Tims and La-Icp Analyses of GJ-1, Plesovice, and FC1 Reference Materials

    NASA Astrophysics Data System (ADS)

    Feldman, J. D.; Möller, A.; Walker, J. D.

    2014-12-01

    Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) U-Pb zircon geochronology relies on external reference standards to monitor and correct for different mass fractionation effects and instrument drift. Common zircon reference materials used within the community, including the KU Isotope Geochemistry Laboratory, are GJ-1 (207Pb/206Pb age: 608.53 +/- 0.37Ma; Jackson et al., 2004), Plesovice (337.13 +/- 0.37 Ma; Slama et al., 2008), and FC-1 (1099.0 +/-0.6 Ma; Paces and Miller, 1993). The age distribution of zircon reference material varies slightly from sample fraction to sample fraction, and the published results for GJ-1 are slightly discordant. As a result, using the published data for the distributed standard splits can lead to small systematic variations when comparing datasets from different labs, and more high precision data are needed to evaluate potential inhomogeneity of sample splits used in different laboratories. Here we characterize these reference materials with cathodoluminescence, LA-ICP-MS traverses across grains, and high precision CA-TIMS to better constrain the ages and assess zoning of these standards, and present the data for comparison with other laboratories. Reducing systematic error by dating our own reference material lends confidence to our analyses and allows for inter-laboratory age reproducibility of unknowns. Additionally, the reduction in propagated uncertainties (especially in GJ-1, for which both the red and yellow variety will be analyzed) will be used to improve long-term reproducibility, comparisons between samples of similar age, detrital populations and composite pluton zircons. Jackson, S.E., et al., 2004, Chemical Geology, v. 211, p. 47-69. Paces, J.B. & Miller, J.D., 1993, Journal of Geophysical Research, v. 80, p. 13997-14013. Slama, J., et al., 2008, Chemical Geology, v. 249. p. 1-35.

  6. 10 CFR 435.3 - Materials incorporated by reference.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... reference the energy performance standards listed in paragraph (b) of this section into 10 CFR part 435. The... incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Any subsequent amendment to a... Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY STANDARDS FOR NEW FEDERAL...

  7. 10 CFR 435.3 - Materials incorporated by reference.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... reference the energy performance standards listed in paragraph (b) of this section into 10 CFR part 435. The... incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Any subsequent amendment to a... Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY STANDARDS FOR NEW FEDERAL...

  8. 10 CFR 435.3 - Materials incorporated by reference.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... reference the energy performance standards listed in paragraph (b) of this section into 10 CFR part 435. The... incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Any subsequent amendment to a... Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY STANDARDS FOR NEW FEDERAL...

  9. Geologic utility of improved orbital measurement capabilities in reference to non-renewable resources

    NASA Technical Reports Server (NTRS)

    Stewart, H.; Marsh, S.

    1982-01-01

    Spectral and spatial characteristics necessary for future orbital remote sensing systems are defined. The conclusions are based on the past decade of experience in exploring for non-renewable resources with reference to data from ground, aircraft, and orbital systems. Two principle areas of investigation are used in the discussion: a structural interpretation in a basin area for hydrocarbon exploration, and a discrimination of altered areas in the Cuprite district in Nevada.

  10. 40 CFR 1045.810 - What materials does this part reference?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... material. Table 1 to this section lists material from the Society of Automotive Engineers that we have... 40 Protection of Environment 34 2013-07-01 2013-07-01 false What materials does this part... Definitions and Other Reference Information § 1045.810 What materials does this part reference?...

  11. 40 CFR 1045.810 - What materials does this part reference?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... material. Table 1 to this section lists material from the Society of Automotive Engineers that we have... 40 Protection of Environment 33 2014-07-01 2014-07-01 false What materials does this part... Definitions and Other Reference Information § 1045.810 What materials does this part reference?...

  12. Evaluation of stream chemistry trends in US Geological Survey reference watersheds, 1970-2010

    USGS Publications Warehouse

    Mast, M. Alisa

    2013-01-01

    The Hydrologic Benchmark Network (HBN) is a long-term monitoring program established by the US Geological Survey in the 1960s to track changes in the streamflow and stream chemistry in undeveloped watersheds across the USA. Trends in stream chemistry were tested at 15 HBN stations over two periods (1970–2010 and 1990–2010) using the parametric Load Estimator (LOADEST) model and the nonparametric seasonal Kendall test. Trends in annual streamflow and precipitation chemistry also were tested to help identify likely drivers of changes in stream chemistry. At stations in the northeastern USA, there were significant declines in stream sulfate, which were consistent with declines in sulfate deposition resulting from the reductions in SO2 emissions mandated under the Clean Air Act Amendments. Sulfate declines in stream water were smaller than declines in deposition suggesting sulfate may be accumulating in watershed soils and thereby delaying the stream response to improvements in deposition. Trends in stream chemistry at stations in other part of the country generally were attributed to climate variability or land disturbance. Despite declines in sulfate deposition, increasing stream sulfate was observed at several stations and appeared to be linked to periods of drought or declining streamflow. Falling water tables might have enhanced oxidation of organic matter in wetlands or pyrite in mineralized bedrock thereby increasing sulfate export in surface water. Increasing sulfate and nitrate at a station in the western USA were attributed to release of soluble salts and nutrients from soils following a large wildfire in the watershed.

  13. Evaluation of stream chemistry trends in US Geological Survey reference watersheds, 1970-2010.

    PubMed

    Mast, M Alisa

    2013-11-01

    The Hydrologic Benchmark Network (HBN) is a long-term monitoring program established by the US Geological Survey in the 1960s to track changes in the streamflow and stream chemistry in undeveloped watersheds across the USA. Trends in stream chemistry were tested at 15 HBN stations over two periods (1970-2010 and 1990-2010) using the parametric Load Estimator (LOADEST) model and the nonparametric seasonal Kendall test. Trends in annual streamflow and precipitation chemistry also were tested to help identify likely drivers of changes in stream chemistry. At stations in the northeastern USA, there were significant declines in stream sulfate, which were consistent with declines in sulfate deposition resulting from the reductions in SO₂ emissions mandated under the Clean Air Act Amendments. Sulfate declines in stream water were smaller than declines in deposition suggesting sulfate may be accumulating in watershed soils and thereby delaying the stream response to improvements in deposition. Trends in stream chemistry at stations in other part of the country generally were attributed to climate variability or land disturbance. Despite declines in sulfate deposition, increasing stream sulfate was observed at several stations and appeared to be linked to periods of drought or declining streamflow. Falling water tables might have enhanced oxidation of organic matter in wetlands or pyrite in mineralized bedrock thereby increasing sulfate export in surface water. Increasing sulfate and nitrate at a station in the western USA were attributed to release of soluble salts and nutrients from soils following a large wildfire in the watershed. PMID:23715732

  14. Evaluation of stream chemistry trends in US Geological Survey reference watersheds, 1970-2010.

    PubMed

    Mast, M Alisa

    2013-11-01

    The Hydrologic Benchmark Network (HBN) is a long-term monitoring program established by the US Geological Survey in the 1960s to track changes in the streamflow and stream chemistry in undeveloped watersheds across the USA. Trends in stream chemistry were tested at 15 HBN stations over two periods (1970-2010 and 1990-2010) using the parametric Load Estimator (LOADEST) model and the nonparametric seasonal Kendall test. Trends in annual streamflow and precipitation chemistry also were tested to help identify likely drivers of changes in stream chemistry. At stations in the northeastern USA, there were significant declines in stream sulfate, which were consistent with declines in sulfate deposition resulting from the reductions in SO₂ emissions mandated under the Clean Air Act Amendments. Sulfate declines in stream water were smaller than declines in deposition suggesting sulfate may be accumulating in watershed soils and thereby delaying the stream response to improvements in deposition. Trends in stream chemistry at stations in other part of the country generally were attributed to climate variability or land disturbance. Despite declines in sulfate deposition, increasing stream sulfate was observed at several stations and appeared to be linked to periods of drought or declining streamflow. Falling water tables might have enhanced oxidation of organic matter in wetlands or pyrite in mineralized bedrock thereby increasing sulfate export in surface water. Increasing sulfate and nitrate at a station in the western USA were attributed to release of soluble salts and nutrients from soils following a large wildfire in the watershed.

  15. 10 CFR 431.95 - Materials incorporated by reference.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... (b) of this section for incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part... International Organization for Standardization, Case Postale 56, CH-1211, Geneva 20, Switzerland....

  16. 40 CFR 1068.95 - What materials does this part reference?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone may inspect copies at the U.S. EPA, Air... material from the Society of Automotive Engineers that we have incorporated by reference. The first column... reference it. Anyone may purchase copies of these materials from the Society of Automotive Engineers,...

  17. Characterization of the Defense Waste Processing Facility (DWPF) Environmental Assessment (EA) glass standard reference material

    SciTech Connect

    Jantzen, C.M.; Bibler, N.E.; Beam, D.C.

    1992-09-30

    Liquid high-level nuclear waste at the Savannah River Site (SRS) will be immobilized by vitrification in borosilicate glass. The glass will be produced and poured into stainless steel canisters in the Defense Waste Processing Facility (DWPF). Other waste form producers, such as West Valley Nuclear Services (WVNS) and the Hanford Waste Vitrification Project (HWVP), will also immobilize high-level radioactive waste in borosilicate glass. The canistered waste will be stored temporarily at each facility for eventual permanent disposal in a geologic repository. The Department of Energy has defined a set of requirements for the canistered waste forms, the Waste Acceptance Preliminary Specifications (WAPS). The current Waste Acceptance Preliminary Specification (WAPS) 1.3, the product consistency specification, requires the waste form producers to demonstrate control of the consistency of the final waste form using a crushed glass durability test, the Product Consistency Test (PCT). In order to be acceptable, a waste glass must be more durable during PCT analysis than the waste glass identified in the DWPF Envirorunental Assessment (EA). In order to supply all the waste form producers with the same standard benchmark glass, 1000 pounds of the EA glass was fabricated. The chemical analyses and characterization of the benchmark EA glass are reported. This material is now available to act as a durability, analytic, and/or redox Standard Reference Material (SRM) for all waste form producers.

  18. Blood plasma reference material: a global resource for proteomic research.

    PubMed

    Malm, Johan; Danmyr, Pia; Nilsson, Rolf; Appelqvist, Roger; Végvári, Akos; Marko-Varga, György

    2013-07-01

    There is an ever-increasing awareness and interest within the clinical research field, creating a large demand for blood fraction samples as well as other clinical samples. The translational research area is another field that is demanding for blood samples, used widely in proteomics, genomics, as well as metabolomics. Blood samples are globally the most common biological samples that are used in a broad variety of applications in life science. We hereby introduce a new reference blood plasma standard (heparin) that is aimed as a global resource for the proteomics community. We have developed these reference plasma standards by defining the Control group as those with C-reactive protein levels <3 mg/L and a Disease group with C-reactive protein ranges >30 mg/L. In these references we have used both newborn children 1-2 weeks, as well as youngsters 15-30 years, and middle aged 30-50 years, and elderly patients at the ages of 65+. In total, there were 80 patients in each group in the reference plasma pools. We provide data on the developments and characteristics of the reference blood plasma standards, as well as what is used by the team members at the respective laboratories. The standards have been evaluated by pilot sample processing in biobanking operations and are currently a resource that allows the Proteomic society to perform quantitative proteomic studies. By the use of high quality reference plasma samples, global initiatives, such as the Chromosome Human Proteome Project (C-HPP), will benefit as one scientific program when the entire human proteome is mapped and linked to human diseases. The plasma reference standards are a global resource and can be accessed upon request. PMID:23701512

  19. Archean, Paleoproterozoic and Mesoproterozoic Crust of Central East Antarctica: New Insights on Subglacial Geology from Proxy Geologic Materials

    NASA Astrophysics Data System (ADS)

    Goodge, J. W.; Fanning, C. M.; Vervoort, J. D.; Fisher, C. M.; Nissen, C. I.

    2013-12-01

    Uncovering the ice-covered geology of East Antarctica is critical for understanding its ancient crustal history, its role in supercontinent formation, and its relationship to development of the Cenozoic ice cap. Multiple approaches--including detrital-mineral provenance study, analysis of glacial clasts, airborne and passive geophysics, and future sub-ice drilling--are rapidly improving our view of the remote continental interior. Proxy geologic materials such as detrital zircons and glacial clasts provide indirect means to sample the ice-covered crust, although spatial-geographic resolution is poor; geophysical data are spatially accurate yet limited by uncertainty in geologic significance. In addition to U-Pb zircon ages of ~3.1, 2.5 and 1.7 Ga from Nimrod Group outcrop, detrital-zircon provenance and glacial clast studies from the central Transantarctic Mountains show that central East Antarctica was formed by a series of episodic magmatic events at 2.01, 1.88-1.79, 1.57, 1.48-1.43, and 1.22-1.06 Ga. Zircon Hf and O isotopic compositions from a suite of granitoid clasts collected from glacial catchments draining central East Antarctica have variable compositions that indicate both juvenile, mantle-derived melts and those involving older crustal sources. None of these igneous clast ages are known from limited Antarctic outcrop in the region. Detrital zircon ages in Neoproterozoic rift-margin strata confirm important populations of 1.88-1.72, 1.64-1.36, and 1.28-1.04 Ga, strengthening a case for episodic magmatic growth of East Antarctic crust. After a juvenile Archean magmatic origin, central East Antarctica was consolidated by further crustal assembly at ~1.9 (Nuna time), ~1.7 (Mawson), and ~1.2 Ga (Rodinia), as indicated by monazite U-Pb ages from metamorphic leucogneiss clasts. Monazite ages record suspected but previously undocumented Proterozoic tectonometamorphic events in central East Antarctica, overprinted by younger Neoproterozoic metamorphism. Together

  20. Determination of halogens, with special reference to iodine, in geological and biological samples using pyrohydrolysis for preparation and inductively coupled plasma mass spectrometry and ion chromatography for measurement.

    PubMed

    Schnetger, B; Muramatsu, Y

    1996-11-01

    A method for determining iodine, bromine, chlorine and fluorine in geological and biological materials is described. In a quartz tube, solid material was heated to 1100 degrees C under a wet oxygen flow (pyrohydrolysis). By this process the halogens (I, Br, Cl, F) were separated from the matrix and then collected in a receiver solution. The chemical yield of iodine was determined by a radioactive tracer. ICP-MS and ion chromatographic measurements were used for the determination of the halogens. The method was optimized by investigating different experimental conditions. All four halogens can be trapped in the receiver solution from one combustion procedure. Precision and accuracy were evaluated by the analysis of environmental standard reference materials (rock, soil, milk, leaves, marine tissue). The concentrations in the materials analysed were in the ranges 0.006-50 mg kg-1 for I, 0.06-1300 mg kg-1 for Br, 50-1100 mg kg-1 for F and 400-11000 mg kg-1 for Cl. The lower values represent the practical detection limit of this method. The results obtained by the proposed method and the certified values are in good agreement.

  1. Determination of halogens, with special reference to iodine, in geological and biological samples using pyrohydrolysis for preparation and inductively coupled plasma mass spectrometry and ion chromatography for measurement.

    PubMed

    Schnetger, B; Muramatsu, Y

    1996-11-01

    A method for determining iodine, bromine, chlorine and fluorine in geological and biological materials is described. In a quartz tube, solid material was heated to 1100 degrees C under a wet oxygen flow (pyrohydrolysis). By this process the halogens (I, Br, Cl, F) were separated from the matrix and then collected in a receiver solution. The chemical yield of iodine was determined by a radioactive tracer. ICP-MS and ion chromatographic measurements were used for the determination of the halogens. The method was optimized by investigating different experimental conditions. All four halogens can be trapped in the receiver solution from one combustion procedure. Precision and accuracy were evaluated by the analysis of environmental standard reference materials (rock, soil, milk, leaves, marine tissue). The concentrations in the materials analysed were in the ranges 0.006-50 mg kg-1 for I, 0.06-1300 mg kg-1 for Br, 50-1100 mg kg-1 for F and 400-11000 mg kg-1 for Cl. The lower values represent the practical detection limit of this method. The results obtained by the proposed method and the certified values are in good agreement. PMID:8952450

  2. Characterisation of reference materials for radioactivity with assigned values traceable to the SI units.

    PubMed

    Altzitzoglou, T; Sibbens, G; Bickel, M; Bohnstedt, A; Decaillon, J-G; Hill, C; Holmes, L

    2004-01-01

    The Institute for Reference Materials and Measurements participates in an IAEA co-ordinated project to upgrade Analytical Quality Control Services intercomparison materials to reference materials. The principal objective is to ensure that assigned property values are traceable to the International System of Units. General principles and practical mechanisms for achieving this traceability are described.

  3. 40 CFR 194.13 - Submission of reference materials.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... PROTECTION PROGRAMS CRITERIA FOR THE CERTIFICATION AND RE-CERTIFICATION OF THE WASTE ISOLATION PILOT PLANT'S COMPLIANCE WITH THE 40 CFR PART 191 DISPOSAL REGULATIONS Compliance Certification and Re-certification... reference books need not to be submitted. Whenever possible, DOE shall submit 10 copies of...

  4. 10 CFR 431.443 - Materials incorporated by reference.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... this section for incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Any....ca/onlinestore/welcome.asp. (1) CAN/CSA-C747-94 (“CAN/CSA-C747”) (Reaffirmed 2005), Energy...

  5. 10 CFR 431.443 - Materials incorporated by reference.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... this section for incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Any....ca/onlinestore/welcome.asp. (1) CSA C747-09 (“CSA C747”), Energy efficiency test methods for...

  6. 10 CFR 431.443 - Materials incorporated by reference.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... this section for incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Any....ca/onlinestore/welcome.asp. (1) CSA C747-09 (“CSA C747”), Energy efficiency test methods for...

  7. 10 CFR 431.95 - Materials incorporated by reference.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... reference. (1) Air-Conditioning and Refrigeration Institute (ARI) Standard 210/240-2003 published in 2003, “Unitary Air-Conditioning and Air-Source Heat Pump Equipment,” IBR approved for § 431.96. (2) ARI Standard 340/360-2004, “Performance Rating of Commercial and Industrial Unitary Air-Conditioning and Heat...

  8. 10 CFR 431.133 - Materials incorporated by reference.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... paragraph (b) of this section for incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR... Ice-Makers.” (2) American National Standards Institute (ANSI)/American Society of Heating.... Department of Energy, Forrestal Building, Room 1J-018 (Resource Room of the Building Technologies...

  9. 40 CFR 600.011-93 - Reference materials.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... Factors Engineering Committee, Society of Automotive Engineers, approved September 1973 as revised... 5 U.S.C. 552(a) and 1 CFR part 51. Copies may be inspected at the U.S. Environmental Protection.... Document number and name 40 CFR part 600 reference ASTM E 29-67 (Reapproved 1973) Standard...

  10. 10 CFR 431.203 - Materials incorporated by reference.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ...) of this section for incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51.... Environmental Protection Agency “ENERGY STAR Program Requirements for Exit Signs,” Version 2.0 issued January 1... Protection Agency “ENERGY STAR Program Requirements for Exit Signs,” Version 2.0, may be obtained from...

  11. 10 CFR 431.203 - Materials incorporated by reference.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ...) of this section for incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51.... Environmental Protection Agency “ENERGY STAR Program Requirements for Exit Signs,” Version 2.0 issued January 1... Protection Agency “ENERGY STAR Program Requirements for Exit Signs,” Version 2.0, may be obtained from...

  12. 10 CFR 431.203 - Materials incorporated by reference.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ...) of this section for incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51.... Environmental Protection Agency “ENERGY STAR Program Requirements for Exit Signs,” Version 2.0 issued January 1... Protection Agency “ENERGY STAR Program Requirements for Exit Signs,” Version 2.0, may be obtained from...

  13. 10 CFR 430.3 - Materials incorporated by reference.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... incorporation by reference by the Director of the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR.... (2) AATCC Test Method 118-2007, Oil Repellency: Hydrocarbon Resistance Test, Revised 2007, IBR... for Nomenclature for Glass Bulbs—Intended for Use with Electric Lamps, approved March 24, 1994,...

  14. 40 CFR 600.011-93 - Reference materials.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... Factors Engineering Committee, Society of Automotive Engineers, approved September 1973 as revised... Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies may be inspected at the U.S... following material is available from the Society of Automotive Engineers. Copies of these materials may...

  15. Determination of total tin in geological materials by electrothermal atomic-absorption spectrophotometry using a tungsten-impregnated graphite furnace

    USGS Publications Warehouse

    Zhou, L.; Chao, T.T.; Meier, A.L.

    1984-01-01

    An electrothermal atomic-absorption spectrophotometric method is described for the determination of total tin in geological materials, with use of a tungsten-impregnated graphite furnace. The sample is decomposed by fusion with lithium metaborate and the melt is dissolved in 10% hydrochloric acid. Tin is then extracted into trioctylphosphine oxide-methyl isobutyl ketone prior to atomization. Impregnation of the furnace with a sodium tungstate solution increases the sensitivity of the determination and improves the precision of the results. The limits of determination are 0.5-20 ppm of tin in the sample. Higher tin values can be determined by dilution of the extract. Replicate analyses of eighteen geological reference samples with diverse matrices gave relative standard deviations ranging from 2.0 to 10.8% with an average of 4.6%. Average tin values for reference samples were in general agreement with, but more precise than, those reported by others. Apparent recoveries of tin added to various samples ranged from 95 to 111% with an average of 102%. ?? 1984.

  16. The group separation of the rare-earth elements and yttrium from geologic materials by cation-exchange chromatography

    USGS Publications Warehouse

    Crock, J.G.; Lichte, F.E.; Wildeman, T.R.

    1984-01-01

    Demand is increasing for the determination of the rare-earth elements (REE) and yttrium in geologic materials. Due to their low natural abundance in many materials and the interferences that occur in many methods of determination, a separation procedure utilizing gradient strong-acid cation-exchange chromatography is often used to preconcentrate and isolate these elements from the host-rock matrix. Two separate gradient strong-acid cation-exchange procedures were characterized and the major elements as well as those elements thought to provide the greatest interference for the determination of the REE in geologic materials were tested for separation from the REE. Simultaneous inductively coupled argon plasma-atomic emission spectroscopy (ICAP-AES) measurements were used to construct the chromatograms for the elution studies, allowing the elution patterns of all the elements of interest to be determined in a single fraction of eluent. As a rock matrix, U.S. Geological Survey standard reference BCR-1 basalt was digested using both an acid decomposition procedure and a lithium metaborate fusion. Hydrochloric and nitric acids were tested as eluents and chromatograms were plotted using the ICAP-AES data; and we observed substantial differences in the elution patterns of the REE and as well as in the solution patterns of Ba, Ca, Fe and Sr. The nitric acid elution required substantially less eluent to elute the REE and Y as a group when compared to the hydrochloric acid elution, and provided a clearer separation of the REE from interfering and matrix elements. ?? 1984.

  17. ECUT energy data reference series: lightweight materials for ground transportation

    SciTech Connect

    Abarcar, R.B.; Hane, G.J.; Johnson, D.R.

    1984-07-01

    This report summarizes information that describes the use of lightweight materials in automobiles. The information on this mode of transportation represents the largest potential energy savings for substitution of lightweight materials in the transportation sector. Included are data on energy conversion efficiency of the engine and its relationship to vehicle weight, the capital stock, the amount of energy used, and the service activity level as measured in ton-miles.

  18. USGS Reference Materials Program: Serving the Needs of the Global Analytical Community

    USGS Publications Warehouse

    Wolf, Ruth E.; Wilson, Stephen A.

    2007-01-01

    Every year in the United States, millions of measurements are made on the chemical composition of items that affect us on a daily basis. The accuracy of these measurements is routinely determined by the analysis of appropriate reference materials. In the field of earth science, reference materials are particularly important because they help us develop a better understanding of the processes that have shaped, and continue to shape the world around us. USGS reference materials are distributed internationally to organizations involved in geochemical and environmental analysis, instrumentation and methods development, and industrial research and quality assurance. Reference materials are widely used in the development and validation of geochemical models used by the USGS.

  19. Homogeneity of the geochemical reference material BRP-1 (paraná basin basalt) and assessment of minimum mass

    USGS Publications Warehouse

    Cotta, Aloisio J. B.; Enzweiler, Jacinta; Wilson, Stephen A.; Perez, Carlos A.; Nardy, Antonio J. R.; Larizzatti, Joao H.

    2007-01-01

    Reference materials (RM) are required for quantitative analyses and their successful use is associated with the degree of homogeneity, and the traceability and confidence limits of the values established by characterisation. During the production of a RM, the chemical characterisation can only commence after it has been demonstrated that the material has the required level of homogeneity. Here we describe the preparation of BRP-1, a proposed geochemical reference material, and the results of the tests to evaluate its degree of homogeneity between and within bottles. BRP-1 is the first of two geochemical RM being produced by Brazilian institutions in collaboration with the United States Geological Survey (USGS) and the International Association of Geoanalysts (IAG). Two test portions of twenty bottles of BRP-1 were analysed by wavelength dispersive-XRF spectrometry and major, minor and eighteen trace elements were determined. The results show that for most of the investigated elements, the units of BRP-1 were homogeneous at conditions approximately three times more rigorous than those strived for by the test of “sufficient homogeneity”. Furthermore, the within bottle homogeneity of BRP-1 was evaluated using small beam (1 mm2) synchrotron radiation XRF spectrometry and, for comparison, the USGS reference materials BCR-2 and GSP-2 were also evaluated. From our data, it has been possible to assign representative minimum masses for some major constituents (1 mg) and for some trace elements (1-13 mg), except Zr in GSP-2, for which test portions of 74 mg are recommended.

  20. Geology and insolation-driven climatic history of Amazonian north polar materials on Mars

    USGS Publications Warehouse

    Tanaka, K.L.

    2005-01-01

    Mariner 9 and Viking spacecraft images revealed that the polar regions of Mars, like those of Earth, record the planet's climate history. However, fundamental uncertainties regarding the materials, features, ages and processes constituting the geologic record remained. Recently acquired Mars Orbiter Laser Altimeter data and Mars Orbiter Camera high-resolution images from the Mars Global Surveyor spacecraft and moderately high-resolution Thermal Emission Imaging System visible images from the Mars Odyssey spacecraft permit more comprehensive geologic and climatic analyses. Here I map and show the history of geologic materials and features in the north polar region that span the Amazonian period (???3.0 Gyr ago to present). Erosion and redeposition of putative circumpolar mud volcano deposits (formed by eruption of liquefied, fine-grained material) led to the formation of an Early Amazonian polar plateau consisting of dark layered materials. Crater ejecta superposed on pedestals indicate that a thin mantle was present during most of the Amazonian, suggesting generally higher obliquity and insolation conditions at the poles than at present. Brighter polar layered deposits rest unconformably on the dark layers and formed mainly during lower obliquity over the past 4-5 Myr (ref. 20). Finally, the uppermost layers post-date the latest downtrend in obliquity <20,000 years ago. ?? 2005 Nature Publishing Group.

  1. Geology and insolation-driven climatic history of Amazonian north polar materials on Mars.

    PubMed

    Tanaka, Kenneth L

    2005-10-13

    Mariner 9 and Viking spacecraft images revealed that the polar regions of Mars, like those of Earth, record the planet's climate history. However, fundamental uncertainties regarding the materials, features, ages and processes constituting the geologic record remained. Recently acquired Mars Orbiter Laser Altimeter data and Mars Orbiter Camera high-resolution images from the Mars Global Surveyor spacecraft and moderately high-resolution Thermal Emission Imaging System visible images from the Mars Odyssey spacecraft permit more comprehensive geologic and climatic analyses. Here I map and show the history of geologic materials and features in the north polar region that span the Amazonian period (approximately 3.0 Gyr ago to present). Erosion and redeposition of putative circumpolar mud volcano deposits (formed by eruption of liquefied, fine-grained material) led to the formation of an Early Amazonian polar plateau consisting of dark layered materials. Crater ejecta superposed on pedestals indicate that a thin mantle was present during most of the Amazonian, suggesting generally higher obliquity and insolation conditions at the poles than at present. Brighter polar layered deposits rest unconformably on the dark layers and formed mainly during lower obliquity over the past 4-5 Myr (ref. 20). Finally, the uppermost layers post-date the latest downtrend in obliquity <20,000 years ago.

  2. Application of Uranium Isotope Dilution Mass Spectrometry in the preparation of New Certified Reference Materials

    NASA Astrophysics Data System (ADS)

    Hasözbek, A.; Mathew, K. J.; Orlowicz, G.; Srinivasan, B.; Narayanan, U.

    2012-04-01

    Proven measurement techniques play a critical role in the preparation of Certified Reference Materials (CRMs) - those requiring high accuracy and precision in the measurement results. Isotope Dilution Mass Spectrometry (IDMS) is one such measurement method commonly used in the quantitative analysis of uranium in nuclear safeguards and isotope geology applications. In this project, we evaluated the possibility of using some of the uranium isotopic and assay CRMs made earlier by the New Brunswick laboratory as IDMS spikes to define the uranium mass fraction in future preparations of CRMs. Uranium solutions prepared from CRM 112-A (a highly pure uranium metal assay standard) and CRM 115 (a highly pure uranium oxide isotopic and assay standard) were used as spikes in the determination of uranium. Two different thermal ionization mass spectrometer instruments (MAT 261 and TRITON) were used for the isotopic measurements. Standard IDMS equation was used for data reduction to yield results for uranium mass fraction along with uncertainties, the latter calculated according to GUM. The results show that uranium mass fraction measurements can be made with the required accuracy and precision for defining the uranium concentration in new CRMs as well as in routine samples analyses.

  3. A fundamental discussion of what triggers localized deformation in geological materials

    NASA Astrophysics Data System (ADS)

    Peters, Max; Paesold, Martin; Poulet, Thomas; Herwegh, Marco; Regenauer-Lieb, Klaus; Veveakis, Manolis

    2015-04-01

    critical amount of dissipative work translated into heat over the diffusive capacity of the system by an instability study designed for such materials (Gruntfest, 1963). With respect to our numerical experiments, this critical parameter determines the timing when the entire amount of deformation energy translated into heat cannot be diffusively transported out of the system anymore. The resulting local temperature rise then induces strain localization. In contrast to classical shear heating scenarios with (catastrophic) thermal runaways, temperature variations of less than 1 K are sufficient for this localization mode to occur due to the balance between heat producing (e.g. dislocation creep) and consuming (grain growth) processes in the present setup. We demonstrate that this rise in latent heat is sufficient to provoke grain growth, operating as an endothermic reaction, stabilizing the simulated localized structure in turn. Various localized ductile structures, such as folded or boudinaged layers, can therefore be placed at the same material failure mode due to fundamental energy bifurcations triggered by dissipative work out of homogeneous state. Finally, we will discuss situations, in which structural heterogeneities are considered negligible and where the energy theory described here plays an underlying role by means of a comparison between numerical experiments and natural examples. REFERENCES Austin, N. and Evans, B. (2007). Paleowattmeters: A scaling relation for dynamically recrystallized grain size. Geology, 35. Gruntfest, I.J. (1963). Thermal feedback in liquid flow, plane shear at constant stress. Transactions of the Society of Rheology, 7. Hansen, L.N. and Zimmermann, M.E. and Dillman, A.M. and Kohlstedt, D.L (2012). Strain localization in olivine aggregates at high temperature: a laboratory comparison of constant-strain-rate and constant-stress boundary conditions. Earth and Planetary Science Letters, 333-334. Herwegh, M., Poulet, T., Karrech, A. and

  4. A fundamental discussion of what triggers localized deformation in geological materials

    NASA Astrophysics Data System (ADS)

    Peters, Max; Paesold, Martin; Poulet, Thomas; Herwegh, Marco; Regenauer-Lieb, Klaus; Veveakis, Manolis

    2015-04-01

    critical amount of dissipative work translated into heat over the diffusive capacity of the system by an instability study designed for such materials (Gruntfest, 1963). With respect to our numerical experiments, this critical parameter determines the timing when the entire amount of deformation energy translated into heat cannot be diffusively transported out of the system anymore. The resulting local temperature rise then induces strain localization. In contrast to classical shear heating scenarios with (catastrophic) thermal runaways, temperature variations of less than 1 K are sufficient for this localization mode to occur due to the balance between heat producing (e.g. dislocation creep) and consuming (grain growth) processes in the present setup. We demonstrate that this rise in latent heat is sufficient to provoke grain growth, operating as an endothermic reaction, stabilizing the simulated localized structure in turn. Various localized ductile structures, such as folded or boudinaged layers, can therefore be placed at the same material failure mode due to fundamental energy bifurcations triggered by dissipative work out of homogeneous state. Finally, we will discuss situations, in which structural heterogeneities are considered negligible and where the energy theory described here plays an underlying role by means of a comparison between numerical experiments and natural examples. REFERENCES Austin, N. and Evans, B. (2007). Paleowattmeters: A scaling relation for dynamically recrystallized grain size. Geology, 35. Gruntfest, I.J. (1963). Thermal feedback in liquid flow, plane shear at constant stress. Transactions of the Society of Rheology, 7. Hansen, L.N. and Zimmermann, M.E. and Dillman, A.M. and Kohlstedt, D.L (2012). Strain localization in olivine aggregates at high temperature: a laboratory comparison of constant-strain-rate and constant-stress boundary conditions. Earth and Planetary Science Letters, 333-334. Herwegh, M., Poulet, T., Karrech, A. and

  5. Household Hazardous Materials and Their Labels: A Reference for Teachers.

    ERIC Educational Resources Information Center

    Dean, Lillian F.

    Household hazardous materials are products or wastes which are toxic, corrosive, reactive, and/or ignitable. Although common products such as pesticides, oils, gasoline, solvents, cleaners, and polishes are hazardous, students and adults are not always aware of potential dangers. This sourcebook contains definitions and examples of household…

  6. 10 CFR 431.15 - Materials incorporated by reference.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... with 5 U.S.C. 552(a) and 1 CFR part 51. Any subsequent amendment to a standard by the standard-setting....gov/buildings/appliance_standards/. Also, this material is available for inspection at the National... 431. (2) (e) NEMA. National Electrical Manufacturers Association, 1300 North 17th Street, Suite...

  7. 49 CFR 572.110 - Materials incorporated by reference.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ....S.C. 552(a) and 1 CFR part 51. Copies of the materials may be inspected at NHTSA's Docket Section... assembly drawing SA-150 M060, revision A, titled “Pelvis and Abdomen Assembly,” dated May 18, 1994....

  8. 49 CFR 572.110 - Materials incorporated by reference.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ....S.C. 552(a) and 1 CFR part 51. Copies of the materials may be inspected at NHTSA's Docket Section... assembly drawing SA-150 M060, revision A, titled “Pelvis and Abdomen Assembly,” dated May 18, 1994....

  9. 49 CFR 572.110 - Materials incorporated by reference.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ....S.C. 552(a) and 1 CFR part 51. Copies of the materials may be inspected at NHTSA's Docket Section... assembly drawing SA-150 M060, revision A, titled “Pelvis and Abdomen Assembly,” dated May 18, 1994....

  10. 49 CFR 572.110 - Materials incorporated by reference.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ....S.C. 552(a) and 1 CFR part 51. Copies of the materials may be inspected at NHTSA's Docket Section... assembly drawing SA-150 M060, revision A, titled “Pelvis and Abdomen Assembly,” dated May 18, 1994....

  11. 49 CFR 572.110 - Materials incorporated by reference.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ....S.C. 552(a) and 1 CFR part 51. Copies of the materials may be inspected at NHTSA's Docket Section... assembly drawing SA-150 M060, revision A, titled “Pelvis and Abdomen Assembly,” dated May 18, 1994....

  12. 10 CFR 431.443 - Materials incorporated by reference.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ....443 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL... material is available for inspection at U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy, Building Technologies Program, Sixth Floor, 950 L'Enfant Plaza, SW., Washington, DC...

  13. 10 CFR 435.3 - Material incorporated by reference.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY STANDARDS FOR NEW FEDERAL LOW-RISE RESIDENTIAL BUILDINGS Mandatory Energy Efficiency Standards for Federal Low-Rise Residential Buildings. § 435... this material by the standard-setting organization will not affect the DOE building energy...

  14. 10 CFR 433.3 - Materials incorporated by reference.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY STANDARDS FOR THE DESIGN AND... organization will not affect the DOE building energy performance standard unless and until DOE amends its building energy performance standards. DOE incorporates the material as it exists on the date specified...

  15. 10 CFR 435.3 - Material incorporated by reference.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY STANDARDS FOR NEW FEDERAL LOW-RISE RESIDENTIAL BUILDINGS Mandatory Energy Efficiency Standards for Federal Low-Rise Residential Buildings. § 435... this material by the standard-setting organization will not affect the DOE building energy...

  16. 10 CFR 433.3 - Materials incorporated by reference.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY STANDARDS FOR THE DESIGN AND... organization will not affect the DOE building energy performance standard unless and until DOE amends its building energy performance standards. DOE incorporates the material as it exists on the date specified...

  17. 10 CFR 431.443 - Materials incorporated by reference.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ....443 Energy DEPARTMENT OF ENERGY ENERGY CONSERVATION ENERGY EFFICIENCY PROGRAM FOR CERTAIN COMMERCIAL... material is available for inspection at U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy, Building Technologies Program, Sixth Floor, 950 L'Enfant Plaza, SW., Washington, DC...

  18. 10 CFR 431.105 - Materials incorporated by reference.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... in accordance with 5 U.S.C. 552(a) and 1 CFR Part 51. Any subsequent amendment to this material by..., “Standard Test Method for Steady-State Heat Flux Measurements and Thermal Transmission Properties by Means... Steady-State Heat Flux Measurements and Thermal Transmission Properties by Means of the...

  19. 10 CFR 431.303 - Materials incorporated by reference.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Any subsequent amendment to a.... Department of Energy, Office of Energy Efficiency and Renewable Energy, Building Technologies Program, 6th... Society for Testing and Materials, 100 Barr Harbor Drive, West Conshohocken, PA 19428-2959, (610)...

  20. 10 CFR 431.75 - Materials incorporated by reference.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Any subsequent amendment to the listed materials by the standard-setting organization will not affect the DOE regulations unless and..., Building Technologies Program, 6th Floor, 950 L'Enfant Plaza SW., Washington, DC 20024, (202) 586-2945,...

  1. 10 CFR 431.263 - Materials incorporated by reference.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Any subsequent amendment to a standard by the standard-setting organization will not affect the DOE regulations unless and until amended by DOE. Material is... Energy Efficiency and Renewable Energy, Building Technologies Program, 6th Floor, 950 L'Enfant Plaza...

  2. 10 CFR 431.95 - Materials incorporated by reference.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... Director of the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Any subsequent amendment to the listed materials by the standard-setting organization will not affect the DOE regulations... Renewable Energy, Building Technologies Program, 6th Floor, 950 L'Enfant Plaza SW., Washington, DC...

  3. Collective Bargaining for Public Managers (State and Local): Reference Materials.

    ERIC Educational Resources Information Center

    Civil Service Commission, Washington, DC. Labor Relations Training Center.

    The book contain pertinent articles on various subjects related to collective bargaining. It was developed and the materials specially written for use by instructors in a collective bargaining course designed to assist public sector managers in attaining a stable and productive labor relations environment. Each article has been keyed to the…

  4. 10 CFR 431.95 - Materials incorporated by reference.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... INDUSTRIAL EQUIPMENT Commercial Air Conditioners and Heat Pumps Test Procedures § 431.95 Materials... published in 1998, “Water-source heat pumps—Testing and rating for performance—Part 1: Water-to-air and...) published in 2004, “Standard for Packaged Terminal Air-Conditioners and Heat Pumps,” IBR approved for §...

  5. Research by the U.S. Geological Survey on organic materials in water

    USGS Publications Warehouse

    Baker, Robert Andrew

    1976-01-01

    The U.S. Geological Survey has responsibility for investigating the Nation's water resources for source, availability, quantity, and quality. This paper describes the Geological Survey's research on organic substances in water and fluvial sediments. Results and ongoing studies are examined. Typical research includes: Separation, concentration, and chromatographic identification of volatile acids; free-flow electrophoresis fractionation of natural organic materials; identification of chlorinated insecticides in suspended sediments and bottom materials; fate of organics following underground disposal; determination of humic and fulvic acid stability constants and characterizations; identification of low-molecular weight chloroorganic constituents in water; PCB (polychlorinated biphenyl compound) distribution in aquatic environments; dissolved organic carbon in ground water; and improvement in separation and concentration schemes prior to analyses.

  6. Multielement analysis of geologic materials by inductively coupled plasma-atomic emission spectroscopy

    SciTech Connect

    Christensen, O.D.; Kroneman, R.L.; Capuano, R.M.

    1980-03-01

    Atomic emission spectroscopy using an inductively coupled plasma (ICP) source permits the rapid acquisition of multielement geochemical data from a wide variety of geologic materials. Rocks or other solid samples are taken into solution with a four acid digestion procedure and introduced directly into the plasma; fluid samples are acidified or analyzed directly. The entire process is computer-controlled, fully-automated, and requires less than five minutes per sample for quantitative determination of 37 elements. The procedures and instrumentation employed at the ESL for multielement ICP analysis of geologic materials are described and these are intended as a guide for evaluating analytic results reported from this laboratory. The quality of geochemical data can be characterized by precision, limits of quantitative determination, and accuracy. Precision values are a measure of the repeatability of analyses. In general, major element and analyses have precision of better than 5% and trace elements of better than 10% of the amount present. (MHR)

  7. Geologic setting of diverse volcanic materials in northern Elysium Planitia, Mars

    NASA Technical Reports Server (NTRS)

    Mouginis-Mark, P. J.

    1990-01-01

    Geologic mapping of high-resolution (30-50 m/pixel) Viking Orbiter images of northern Elysium Planitia has identified seven sites where current problems in martian volcanology, chronology, and stratigraphy can be resolved. These sites, which are discussed in the context of a potential Mars rover/sample return mission, would permit the following investigations: (1) the dating of Lower Amazonian lava flows from Elysium Mons (thereby providing absolute calibration for global crater size/frequency relative chronologies, (2) the petrologic investigation of long run-out lava flows, (3) the geologic interpretation of materials that may either be lava flows or lahar deposits, (4) the analysis of materials believed to be ash deposits produced by explosive eruptions of Hecates Tholus, and (5) the investigation of the stratigraphy of fractured terrain along the boundary between northern Elysium Planitia and southern Utopia Planitia.

  8. Dynamic simulations of geologic materials using combined FEM/DEM/SPH analysis

    SciTech Connect

    Morris, J P; Johnson, S M

    2008-03-26

    An overview of the Lawrence Discrete Element Code (LDEC) is presented, and results from a study investigating the effect of explosive and impact loading on geologic materials using the Livermore Distinct Element Code (LDEC) are detailed. LDEC was initially developed to simulate tunnels and other structures in jointed rock masses using large numbers of polyhedral blocks. Many geophysical applications, such as projectile penetration into rock, concrete targets, and boulder fields, require a combination of continuum and discrete methods in order to predict the formation and interaction of the fragments produced. In an effort to model this class of problems, LDEC now includes implementations of Cosserat point theory and cohesive elements. This approach directly simulates the transition from continuum to discontinuum behavior, thereby allowing for dynamic fracture within a combined finite element/discrete element framework. In addition, there are many application involving geologic materials where fluid-structure interaction is important. To facilitate solution of this class of problems a Smooth Particle Hydrodynamics (SPH) capability has been incorporated into LDEC to simulate fully coupled systems involving geologic materials and a saturating fluid. We will present results from a study of a broad range of geomechanical problems that exercise the various components of LDEC in isolation and in tandem.

  9. Atomic-absorption spectrochemical analysis for ultratrace elements in geological materials by hydride-forming techniques: Selenium.

    PubMed

    Sighinolfi, G P; Gorgoni, C

    1981-03-01

    A method based on hydride generation for the AAS determination of selenium at nanogram levels in geological materials is described. The sample is decomposed by aqua regia attack in a sealed Teflon bomb. After treatment with hydrochloric acid, selenium is converted into hydrogen selenide by reaction with sodium borohydride and determined by AAS. Matrix interference effects have been investigated, but though they are rarely significant, the standard-additions method is recommended. The absolute sensitivity of the method is about 2.0 ng of Se (in 10 ml of solution). Detection limits of about 5-10 ng in a 1.0-g sample have been achieved with the use of "Suprapure" reagents. The selenium content of some USGS, CRPG and ANRT reference samples is reported. PMID:18962885

  10. Atomic-absorption spectrochemical analysis for ultratrace elements in geological materials by hydride-forming techniques: Selenium.

    PubMed

    Sighinolfi, G P; Gorgoni, C

    1981-03-01

    A method based on hydride generation for the AAS determination of selenium at nanogram levels in geological materials is described. The sample is decomposed by aqua regia attack in a sealed Teflon bomb. After treatment with hydrochloric acid, selenium is converted into hydrogen selenide by reaction with sodium borohydride and determined by AAS. Matrix interference effects have been investigated, but though they are rarely significant, the standard-additions method is recommended. The absolute sensitivity of the method is about 2.0 ng of Se (in 10 ml of solution). Detection limits of about 5-10 ng in a 1.0-g sample have been achieved with the use of "Suprapure" reagents. The selenium content of some USGS, CRPG and ANRT reference samples is reported.

  11. 40 CFR 1060.810 - What materials does this part reference?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Federal Register approved the incorporation by reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part.... (a) ASTM material. Table 1 to this section lists material from the American Society for Testing and... these materials from the American Society for Testing and Materials, 100 Barr Harbor Dr., P.O. Box...

  12. 40 CFR 1068.95 - What materials does this part reference?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... material. Table 1 to this section lists material from the Society of Automotive Engineers that we have... 40 Protection of Environment 34 2013-07-01 2013-07-01 false What materials does this part... and Miscellaneous Provisions § 1068.95 What materials does this part reference? Documents listed...

  13. 40 CFR 1068.95 - What materials does this part reference?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... material. Table 1 to this section lists material from the Society of Automotive Engineers that we have... 40 Protection of Environment 33 2014-07-01 2014-07-01 false What materials does this part... and Miscellaneous Provisions § 1068.95 What materials does this part reference? Documents listed...

  14. 40 CFR 1060.810 - What materials does this part reference?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... material. Table 2 to this section lists material from the Society of Automotive Engineers that we have... 40 Protection of Environment 33 2014-07-01 2014-07-01 false What materials does this part... EQUIPMENT Definitions and Other Reference Information § 1060.810 What materials does this part...

  15. [Latin American regional reference materials for porcine heparin and bovine heparin].

    PubMed

    Albertengo, M E; Cinto, R O; Araldi, H T; Vernengo, M J

    1990-02-01

    In agreement with the Regional Programme of Reference Materials of the Panamerican Health Organization the Instituto Nacional de Farmacología y Bromatología of Buenos Aires designed a study for the calibration of a Reference Material for Heparin, porcine, mucosal and a Reference Material for Heparin, bovine, mucosal. The assay methods used in this study were those described in the United States Pharmacopeia XXI Ed and British Pharmacopoeia 1980, Addendum 1983. The overall combined potency estimates of both heparin in preparations relative to 4th Int.St. was 1633.83 UI/ampoule (95% confidence limits 1609.70-1657.96 UI/ampoule) for porcine heparin and 1332.31 UI/ampoule (95% confidence limits, 1302.31-1361.77 UI/ampoule) for bovine heparin. The assigned unitage was 1630 UI/ampoule for the porcine Reference Material and 1330 UI/ampoule for the bovine Reference Material.

  16. Evolutionary design of bone scaffolds with reference to material selection.

    PubMed

    Heljak, M K; Swięszkowski, W; Lam, C X F; Hutmacher, D W; Kurzydłowski, K J

    2012-01-01

    The favourable scaffold for bone tissue engineering should have desired characteristic features, such as adequate mechanical strength and three-dimensional open porosity, which guarantee a suitable environment for tissue regeneration. In fact, the design of such complex structures like bone scaffolds is a challenge for investigators. One of the aims is to achieve the best possible mechanical strength-degradation rate ratio. In this paper we attempt to use numerical modelling to evaluate material properties for designing bone tissue engineering scaffold fabricated via the fused deposition modelling technique. For our studies the standard genetic algorithm was used, which is an efficient method of discrete optimization. For the fused deposition modelling scaffold, each individual strut is scrutinized for its role in the architecture and structural support it provides for the scaffold, and its contribution to the overall scaffold was studied. The goal of the study was to create a numerical tool that could help to acquire the desired behaviour of tissue engineered scaffolds and our results showed that this could be achieved efficiently by using different materials for individual struts. To represent a great number of ways in which scaffold mechanical function loss could proceed, the exemplary set of different desirable scaffold stiffness loss function was chosen.

  17. Satellite Contamination and Materials Outgassing Knowledgebase - An Interactive Database Reference

    NASA Technical Reports Server (NTRS)

    Green, D. B.; Burns, Dewitt (Technical Monitor)

    2001-01-01

    The goal of this program is to collect at one site much of the knowledge accumulated about the outgassing properties of aerospace materials based on ground testing, the effects of this outgassing observed on spacecraft in flight, and the broader contamination environment measured by instruments on-orbit. We believe that this Web site will help move contamination a step forward, away from anecdotal folklore toward engineering discipline. Our hope is that once operational, this site will form a nucleus for information exchange, that users will not only take information from our knowledge base, but also provide new information from ground testing and space missions, expanding and increasing the value of this site to all. We urge Government and industry users to endorse this approach that will reduce redundant testing, reduce unnecessary delays, permit uniform comparisons, and permit informed decisions.

  18. Reference materials and intercomparison samples available from the Environmental Monitoring Systems Laboratory - Las Vegas

    SciTech Connect

    Kantor, E.J.; Laska, P.R.

    1985-06-01

    Reference materials and intercomparison samples may be obtained by laboratories involved in the analysis of environmental samples containing radioactivity, pesticides, toxic inorganic species, or toxic organic species. These reference materials and intercomparison samples are available from the US Environmental Protection Agency's Quality Assurance Division located at the Environmental Monitoring Systems Laboratory in Las Vegas (EMSL-LV). These materials are useful for incorporation into a laboratory's quality control program for the evaluation of the precision and accuracy of analytical work. Media used for radiation reference materials are pitchblende, Monazite ore, uranium mill tailings, Mancos shale, fly ash, and water spiked with radionuclides. Radioactivity intercomparison samples consist of water, milk, air, urine, and a simulated diet slurry spiked with radionuclides. Media available for toxic organic reference materials are sludge, shale oil, and rag oil, and for intercomparison samples are soil and water. Characterized fly ash, foundry sludge, and river sediment serve as reference materials for toxic inorganics, while spiked soil and water serve as intercomparison samples. Finally, spiked adipose tissue, blood plasma, urine, and water comprise the pesticide intercomparison samples, and, after the disclosure of the true pesticide compositions and concentrations of these samples, the laboratory can use the samples as reference materials. The reference materials are generally available continuously, but the intercomparison samples are distributed on a scheduled basis and in some cases only to certain laboratories. 9 tables.

  19. Multi-block analysis coupled to laser-induced breakdown spectroscopy for sorting geological materials from caves.

    PubMed

    Ammari, Faten; Bassel, Léna; Ferrier, Catherine; Lacanette, Delphine; Chapoulie, Rémy; Bousquet, Bruno

    2016-10-01

    In this study, multi-block analysis was applied for the first time to LIBS spectra provided by a portable LIBS system (IVEA Solution, France) equipped with three compact Czerny-Turner spectrometers covering the spectral ranges 200-397nm, 398-571nm and 572-1000nm. 41 geological samples taken from a laboratory-cave situated in the "Vézère valley", an area rich with prehistoric sites and decorated caves listed as a UNESCO world heritage in the south west of France, were analyzed. They were composed of limestone and clay considered as underlying supports and of two types of alterations referred as moonmilk and coralloid. Common Components and Specific Weights Analysis (CCSWA) allowed sorting moonmilk and coralloid samples. The loadings revealed higher amounts of magnesium, silicon, aluminum and strontium in coralloids and the saliences emphasized that among the three spectrometers installed in the LIBS instrument used in this work; that covering the range 572-1000nm was less contributive. This new approach for processing LIBS data not only provides good results for sorting geological materials but also clearly reveals which spectral range contains most of the information. This specific advantage of multi-block analysis could lead for some applications to simplify the design and to reduce the size of LIBS instruments. PMID:27474310

  20. New biological reference materials - in vivo incorporated toxic metals in water hyacinth tissues

    SciTech Connect

    Austin, J.R.; Simon, S.J.; Williams, L.R.; Beckert, W.F.

    1985-06-01

    The purpose of this study was to demonstrate that high-quality reference materials, containing high levels of multiple toxic elements, can be produced with in vivo incorporation procedures. The approach taken was to produce water hyacinth tissue materials - leaves and stems containing high levels of arsenic, cadmium, lead, and mercury - as follows: apply a hydroponic feeding procedure for the in vivo incorporation of toxic elements into water hyacinths; dry, blend, and homogenize the plant materials and determine the levels of the incorporated elements and the homogeneity of the generated plant material; demonstrate that low-level control materials can be successfully blended with high-level materials to yield a homogeneous material with intermediate toxicant levels; evaluate the precision of the analytical methods used to determine toxic element levels in the materials; and evaluate the stability of the resulting materials. Sufficient quantities of the parent materials were produced so that characterized reference materials can now be made available on request. Levels of the toxic elements incorporated in water hyacinth leaves were 100, 300, 60, and 27 times the levels present in the control leaves for arsenic, cadmium, lead, and mercury, respectively. Overall precision of sampling, subsampling, and digestion, and chemical analysis of the treated materials, ranged from 3 to 10% relative standard deviation and was generally comparable to that of three NBS biological reference materials tested. 3 references, 1 figure, 4 tables.

  1. Applications of New Synthetic Uranium Reference Materials for Geochemistry Research (Invited)

    NASA Astrophysics Data System (ADS)

    Richter, S.; Weyer, S.; Alonso, A.; Aregbe, Y.; Kuehn, H.; Eykens, R.; Verbruggen, A.; Wellum, R.

    2009-12-01

    For many applications in geochemistry research isotope ratio measurements play a significant role. In geochronology isotope abundances of uranium and its daughter products thorium and lead are being used to determine the age and history of various samples of geological interest. For measuring the isotopic compositions of these elements by mass spectrometry, suitable isotope reference materials are needed to validate measurement procedures and to calibrate multi-collector and ion counting detector systems. IRMM is a recognized provider for nuclear isotope reference materials to the nuclear industry and nuclear safeguards authorities, which are also being applied widely for geochemical applications. The preparation of several new synthetic uranium reference materials at IRMM during the recent five years has provided significant impacts on geochemical research. As an example, the IRMM-074 series of gravimetrically prepared uranium mixtures for linearity testing of secondary electron multipliers (SEMs) has been applied for the redetermination of the secular equilibrium 234U/238U value and the 234U half-life by Cheng et al (2009). Due to the use of IRMM-074, results with smaller uncertainties were obtained, which are shifted by about 0.04% compared to the commonly used values published earlier by Cheng et al. in 2000. This has a significant impact for U isotope measurements in geochemistry.. As a further example, the new double spike IRMM-3636 with a 233U/236U ratio of 1:1 and an expanded uncertainty as low as 0.016% (coverage factor k=2, 95% confidence level) was prepared gravimetrically. This double spike allows internal mass fractionation correction for high precision 235U/238U ratio measurements of close to natural samples. Using the new double spike IRMM-3636, the 235U/238U ratios for several commonly used natural U standard materials from NIST/NBL and IRMM, such as e.g. NBS960 (=NBL CRM-112a), NBS950a,b and IRMM-184, have been re-measured with improved precision

  2. Multispectral Microscopic Imager (MMI): Multispectral Imaging of Geological Materials at a Handlens Scale

    NASA Astrophysics Data System (ADS)

    Farmer, J. D.; Nunez, J. I.; Sellar, R. G.; Gardner, P. B.; Manatt, K. S.; Dingizian, A.; Dudik, M. J.; McDonnell, G.; Le, T.; Thomas, J. A.; Chu, K.

    2011-12-01

    The Multispectral Microscopic Imager (MMI) is a prototype instrument presently under development for future astrobiological missions to Mars. The MMI is designed to be a arm-mounted rover instrument for use in characterizing the microtexture and mineralogy of materials along geological traverses [1,2,3]. Such geological information is regarded as essential for interpreting petrogenesis and geological history, and when acquired in near real-time, can support hypothesis-driven exploration and optimize science return. Correlated microtexure and mineralogy also provides essential data for selecting samples for analysis with onboard lab instruments, and for prioritizing samples for potential Earth return. The MMI design employs multispectral light-emitting diodes (LEDs) and an uncooled focal plane array to achieve the low-mass (<1kg), low-cost, and high reliability (no moving parts) required for an arm-mounted instrument on a planetary rover [2,3]. The MMI acquires multispectral, reflectance images at 62 μm/pixel, in which each image pixel is comprised of a 21-band VNIR spectrum (0.46 to 1.73 μm). This capability enables the MMI to discriminate and resolve the spatial distribution of minerals and textures at the microscale [2, 3]. By extending the spectral range into the infrared, and increasing the number of spectral bands, the MMI exceeds the capabilities of current microimagers, including the MER Microscopic Imager (MI); 4, the Phoenix mission Robotic Arm Camera (RAC; 5) and the Mars Science Laboratory's Mars Hand Lens Imager (MAHLI; 6). In this report we will review the capabilities of the MMI by highlighting recent lab and field applications, including: 1) glove box deployments in the Astromaterials lab at Johnson Space Center to analyze Apollo lunar samples; 2) GeoLab glove box deployments during the 2011 Desert RATS field trials in northern AZ to characterize analog materials collected by astronauts during simulated EVAs; 3) field deployments on Mauna Kea

  3. Embrapa's experience in the production and development of agriculture reference materials

    NASA Astrophysics Data System (ADS)

    Nogueira, A. R. A.; Souza, G. B.; Bossu, C. M.; Bianchi, S. R.; Verhalen, T. R.; Silva, P. T.; Peixoto, A. A. J.; Silva, C. S.

    2016-07-01

    The main challenge of Embrapa is to develop a model of genuine Brazilian tropical agriculture and livestock. To get this task, the quality of laboratories results is mandatory, increasing the demand for reference materials. Projects were proposed to produce reference materials to support the national agriculture laboratories and consolidate a network able to perform reliable and reproducible analytical testing laboratory within the internationally standards required. Reference materials were produced and available to interested laboratories and collaborative tests were conducted to obtain consensus values. The results and statistical evaluations were performed with the use of software developed by Embrapa Pecuaria Sudeste.

  4. Quality assurance of environmental organic analysis in the absence of certified reference materials

    SciTech Connect

    Hoover, D.; Hamilton, C.; Fowler, B.

    1995-12-31

    Reference materials of characteristic matrix with certified concentrations of analytes are normally cornerstones of analytical quality assurance programs. Environmental analytical chemists face a special challenge in producing accurate and defensible trace analysis data supported by only a limited number of suitable certified reference materials (CRMs) with which to validate methodology. In the absence of CRMs the analyst turns to other means of validating method performance. These may include the use of isotopically labelled standards, matrix spikes, recovery studies, intercalibration exercises and the use of ancillary reference materials. This paper describes the various data validation procedures available with emphasis on understanding and interpretation of the results by data users.

  5. Basic petroleum geology, 2nd ed. , revised

    SciTech Connect

    Link.

    1990-01-01

    This book contains revised and updated material, including approximately 200 additional illustrations and an extensive glossary of terms. A valuable reference for geology students and petroleum professionals, the text presents fundamental concepts of geology in terms of sedimentary deposition, petroleum occurrence, exploration, and recovery. This book contains information on geologic time, historical geology and stratigraphy; Minerals and rocks; Weathering erosion, and deposition; Marine erosion and deposition; Depositional basins; Lacustrine, desert and glacial environments; Subsurface water and diagenesis; Structural geology; petroleum traps; Petroleum and reservoirs; Geological considerations and engineering practices; Rocks, reservoirs, and recovery techniques; Exploration techniques for petroleum; Bibliography Glossary; Index.

  6. New Organic Stable Isotope Reference Materials for Distribution through the USGS and the IAEA

    NASA Astrophysics Data System (ADS)

    Schimmelmann, Arndt; Qi, Haiping

    2014-05-01

    The widespread adoption of relative stable isotope-ratio measurements in organic matter by diverse scientific disciplines is at odds with the dearth of international organic stable isotopic reference materials (RMs). Only two of the few carbon (C) and nitrogen (N) organic RMs, namely L-glutamic acids USGS40 and USGS41 [1], both available from the U.S. Geological Survey (USGS) and the International Atomic Energy Agency (IAEA), provide an isotopically contrasting pair of organic RMs to enable essential 2-point calibrations for δ-scale normalization [2, 3]. The supply of hydrogen (H) organic RMs is even more limited. Numerous stable isotope laboratories have resorted to questionable practices, for example by using 'CO2, N2, and H2 reference gas pulses' for isotopic calibrations, which violates the principle of identical treatment of sample and standard (i.e., organic unknowns should be calibrated directly against chemically similar organic RMs) [4], or by using only 1 anchor instead of 2 for scale calibration. The absence of international organic RMs frequently serves as an excuse for indefensible calibrations. In 2011, the U.S. National Science Foundation (NSF) funded an initiative of 10 laboratories from 7 countries to jointly develop much needed new organic RMs for future distribution by the USGS and the IAEA. The selection of targeted RMs attempts to cover various common compound classes of broad technical and scientific interest. We had to accept compromises to approach the ideal of high chemical stability, lack of toxicity, and low price of raw materials. Hazardous gases and flammable liquids were avoided in order to facilitate international shipping of future RMs. With the exception of polyethylene and vacuum pump oil, all organic RMs are individual, chemically-pure substances, which can be used for compound-specific isotopic measurements in conjunction with liquid and gas chromatographic interfaces. The compounds listed below are under isotopic calibration by

  7. Arsenic species in certified reference material MURST-ISS-A2 (Antarctic krill).

    PubMed

    Grotti, Marco; Soggia, Francesco; Goessler, Walter; Findenig, Silvia; Francesconi, Kevin A

    2010-01-15

    Arsenic compounds were quantified in the certified reference material MURST-ISS-A2 (Antarctic krill) using HPLC/ICPMS. The data should prove useful for assessing the accuracy of arsenic speciation procedures.

  8. REFERENCE MATERIALS AND QUALITY ASSURANCE FOR THE CHARACTERIZATION OF ORGANIC COMPOUNDS IN PARTICULATE MATTER

    EPA Science Inventory

    One of the first environmental matrix Standard Reference Materials (SRMs) developed by the National Institute of Standards and Technology (NIST) for determination of organic species was SRM 1649 Urban Dust, ambient total suspended particulate matter (PM) collected in Washington D...

  9. 40 CFR 1060.810 - What materials does this part reference?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... Federal Register approved the incorporation by reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part... Materials Document number and name Part 1060reference ASTM D471-06, Standard Test Method for Rubber Property—Effect of Liquids (“ASTM D471”) 1060.515 ASTM D2862-97 (Reapproved 2004), Standard Test Method...

  10. Compilation of elemental concentration data for the United States geological survey's six geochemical exploration reference materials

    SciTech Connect

    Gladney, E.S.

    1980-08-01

    Elemental composition data on USGS GXR1 ..-->.. GXR6 have been collected and summarized from 13 journal papers and reports. Data from one report concerning the influence of rock dissolution method on subsequent atomic absorption analysis are summarized for aluminium, silver, calcium, iron, and manganese.

  11. Sixth IASLIC Seminar Papers. Part I: Reference Service-in-Action. Part II: Processing & Servicing of Special Materials in Libraries.

    ERIC Educational Resources Information Center

    Indian Association of Special Libraries & Information Centres, Calcutta (India).

    Part I contains 22 papers covering all aspects of the library reference services including sources of reference materials, an evaluation of reference sources, building a reference collection, training a reference librarian, and the needs of the industrial and medical communities for reference services. All the papers are slanted toward the special…

  12. Simplified method for the determination of Ru, Pd, Re, Os, Ir and Pt in chromitites and other geological materials by isotope dilution ICP-MS and acid digestion.

    PubMed

    Meisel, T; Moser, J; Fellner, N; Wegscheider, W; Schoenberg, R

    2001-03-01

    A method for the determination of low Ru, Pd, Re, Os, Ir and Pt abundances in geological reference materials by isotope dilution inductively coupled plasma mass spectrometry (ICP-MS) after acid digestion in a high pressure asher (HPA-S) is presented. The digestion technique is similar to that using Carius tubes but easier to handle and reaches higher temperatures. Osmium can be determined as OsO4 with ICP-MS directly after digestion through a sparging technique. The remaining elements are preconcentrated by means of anion column chromatography. The resin is digested directly without elution leading to high yields but this causes problems if Zr is present at higher levels in the silicate rich materials. The analytical results for international platinum group element (PGE) reference materials, chromitite CHR-Bkg, basalt TDB-1 and gabbro WGB-1, are presented and compared with literature data, demonstrating the validity of the described method. Although higher in concentration, PGEs determined for reference material WGB-1 were worse than for TDB-1 indicating a more inhomogeneous distribution of the platinum group mineral phases. The low PGE abundance chromitite standard, CHR-Bkg, is likely to be homogeneous for Ru, Re, Os and Ir and is recommended as a reference material for the study of chromitites. Detection limits (3s x total procedure blank) range from 0.012 ng (Re and Os) to 0.77 ng (Pt), which could be further improved by applying higher quality acids.

  13. Simplified method for the determination of Ru, Pd, Re, Os, Ir and Pt in chromitites and other geological materials by isotope dilution ICP-MS and acid digestion.

    PubMed

    Meisel, T; Moser, J; Fellner, N; Wegscheider, W; Schoenberg, R

    2001-03-01

    A method for the determination of low Ru, Pd, Re, Os, Ir and Pt abundances in geological reference materials by isotope dilution inductively coupled plasma mass spectrometry (ICP-MS) after acid digestion in a high pressure asher (HPA-S) is presented. The digestion technique is similar to that using Carius tubes but easier to handle and reaches higher temperatures. Osmium can be determined as OsO4 with ICP-MS directly after digestion through a sparging technique. The remaining elements are preconcentrated by means of anion column chromatography. The resin is digested directly without elution leading to high yields but this causes problems if Zr is present at higher levels in the silicate rich materials. The analytical results for international platinum group element (PGE) reference materials, chromitite CHR-Bkg, basalt TDB-1 and gabbro WGB-1, are presented and compared with literature data, demonstrating the validity of the described method. Although higher in concentration, PGEs determined for reference material WGB-1 were worse than for TDB-1 indicating a more inhomogeneous distribution of the platinum group mineral phases. The low PGE abundance chromitite standard, CHR-Bkg, is likely to be homogeneous for Ru, Re, Os and Ir and is recommended as a reference material for the study of chromitites. Detection limits (3s x total procedure blank) range from 0.012 ng (Re and Os) to 0.77 ng (Pt), which could be further improved by applying higher quality acids. PMID:11284333

  14. Applications of New Synthetic Uranium Reference Materials for Research in Geochemistry

    NASA Astrophysics Data System (ADS)

    Richter, Stephan; Alonso, Adolfo; Aregbe, Yetunde; Eykens, Roger; Jacobsson, Ulf; Kuehn, Heinz; Verbruggen, Andre; Weyer, Stefan

    2010-05-01

    For many applications in geochemistry research isotope ratio measurements play a significant role. In geochronology isotope abundances of uranium and its daughter products thorium and lead are being used to determine the age and history of various samples of geological interest. For measuring the isotopic compositions of these elements by mass spectrometry, suitable isotope reference materials are needed to validate measurement procedures and to calibrate multi-collector and ion counting detector systems. IRMM is a recognized provider for nuclear isotope reference materials to the nuclear industry and nuclear safeguards authorities, which are also being applied widely for geochemical applications. Firstly, the double spike IRMM-3636 with a 233U/236U ratio of 1:1 was prepared which allows internal mass fractionation correction for high precision 235U/238U ratio measurements. The 234U abundance of this double spike material is low enough to allow an accurate and precise correction of 234U/238U ratios, even for measurements of close to equilibrium uranium samples. The double spike IRMM-3636 is offered in 3 concentrations: 1mg/g, 0.1mg/g and 0.005mg/g. Secondly, the 236U single spike IRMM-3660 was prepared and is offered in 3 concentrations: 1mg/g, 0.1mg/g and 0.01mg/g. Thirdly, a "Quad"-isotope reference material, IRMM-3101, has been prepared which is characterized by 233U/235U/236U/238U=1/1/1/1. This material is useful for checking Faraday cup efficiencies and inter-calibration of MIC (multiple ion counting) detectors. The quad-IRM is offered in 3 concentrations: 1mg/g, 0.1mg/g and 0.01mg/g. As one example for the significant influence of synthetic reference materials for geochemical research, the IRMM-074 series of gravimetrically prepared uranium mixtures for linearity testing of secondary electron multipliers (SEMs) has been applied for the redetermination of the secular equilibrium 234U/238U value and the 234U half-life by Cheng et al (2009). Due to the use of

  15. Atomic absorption spectrometric determination of copper, zinc, and lead in geological materials

    USGS Publications Warehouse

    Sanzolone, R.F.; Chao, T.T.

    1976-01-01

    An atomic absorption spectrometric method is described for the determination of copper, zinc, and lead in geological materials. The sample is digested with HF-HCl-H2O2; the final solution for analysis is in 10 % (v/v) HCl. Copper and zinc are determined directly by aspirating the solution into an air-acetylene flame. A separate aliquot of the solution is used for determination of lead; lead is extracted into TOPO-MIBK from the acidic solution in the presence of iodide and ascorbic acid. For a 0.50-g sample, the limits of determination are 10-2000 p.p.m. for Cu and Zn, and 5-5000 p.p.m. for Pb. As much as 40 % Fe or Ca. and 10 % Al, Mg, or Mn in the sample do not interfere. The proposed method can be applied to the determination of copper, zinc, and lead in a wide range of geological materials including iron- and manganese-rich, calcareous and carbonate samples. ?? 1976.

  16. Methods for TEM analysis of NIST's single-walled carbon nanotube Standard Reference Material

    NASA Astrophysics Data System (ADS)

    Mansfield, Elisabeth; Geiss, Roy; Fagan, Jeffrey A.

    2009-08-01

    The National Institute of Standards and Technology (NIST) will soon release a series of single-walled carbon nanotube (SWCNT) reference materials (RMs) to provide users with a well-characterized material for their applications. The SWCNT reference material will be introduced as a series of three types of material: (1) raw soot characterized for composition, which will be certified as a Standard Reference Material, (2) purified (greater than 90 % SWCNT by weight) bucky paper and (3) dispersed, length-sorted populations characterized by length. The instrumental characterization of NIST's SWCNT reference materials is extensive, and this paper aims to provide researchers with dispersion preparation methods for TEM (transmission electron microscopy) analysis of the SWCNT raw soot. A selection of dispersing solvents, including organic solvents, aqueous surfactants and DNA dispersions, were prepared and examined by TEM. Recommendations for sample preparation of the SWCNT SRM 2483 to yield images similar to those presented here are given. Examples of images of the length-sorted SWCNT reference material are also shown. These results illustrate the importance of optimal dispersion to enable imaging of SWCNT characteristics.

  17. A Reference List of Audiovisual Materials Produced by the United States Government, 1978.

    ERIC Educational Resources Information Center

    National Archives and Records Service (GSA), Washington, DC. National Audiovisual Center.

    This reference guide describes over 6,000 audiovisual materials selected from more than 10,000 programs produced by 175 federal agencies covering a wide range of subjects, including medicine, dentistry, allied health, education, science, social studies, industrial technology/training, safety, and the environmental sciences. Materials are cited by…

  18. Determination of Perfluorinated Alkyl Acid Concentrations in Biological Standard Reference Materials

    EPA Science Inventory

    Standard reference materials (SRMs) are homogeneous, well-characterized materials used to validate measurements and improve the quality of analytical data. The National Institute of Standards and Technology (NIST) has a wide range of SRMs that have mass fraction values assigned ...

  19. 40 CFR 1045.810 - What materials does this part reference?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Register approved the incorporation by reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone... material. Table 1 to this section lists material from the Society of Automotive Engineers that we have... the Society of Automotive Engineers, 400 Commonwealth Drive, Warrendale, PA 15096 or...

  20. 40 CFR 1068.95 - What materials does this part reference?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... approved the incorporation by reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone may... material. Table 1 to this section lists material from the Society of Automotive Engineers that we have... the Society of Automotive Engineers, 400 Commonwealth Drive, Warrendale, PA 15096 or...

  1. Certificate of Analysis, Standard Reference Material® 1849, Infant/Adult Nutritional Formula

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Standard Reference material (SRM) 1849 is intended primarily for validation of methods for determining proximates, fatty acids, vitamins, elements and nucleotides in infant and adult nutritional formulas and similar materials. This SRM can also be used for quality assurance when assigning values to ...

  2. Sources of Audiovisual Materials about Handicapping Conditions. Reference Circular No. 85-3.

    ERIC Educational Resources Information Center

    Library of Congress, Washington, DC. National Library Service for the Blind and Physically Handicapped.

    The reference circular lists sources of audiovisual materials on handicapping conditions with separate sections on adults and children. The materials, which include films, videocassettes, and slides address such adult-related topics as accessibility, arthritis, attitudes toward disabled persons, communication, deafness, mainstreaming, employment,…

  3. Geologic and hydrologic features of the San Bernardino area, California - with special reference to underflow across the San Jacinto fault

    USGS Publications Warehouse

    Dutcher, L.C.; Garrett, Arthur A.

    1963-01-01

    This is the second in a series of interpretive reports on subsurface outflow from the ground-water basins of San Bernardino County, Calif., prepared by the U.S. Geological Survey in cooperation with the San Bernardino County Flood Control District. One principal purpose of the study was to estimate the ground-water outflow from the Bunker Hill basin to the Rialto-Colton basin across the San Jacinto fault, which, except locally, forms a nearly impermeable boundary between the two basins. In addition, the report deals qualitatively with the geology, the fault barriers that divide the area into several ground-water basins, the physical nature and degree of imperviousness of the barriers, the occurrence and movement of ground water and fluctuations of water level in the basins, and the chemical quality of surface and ground waters in the San Bernardino area. The report includes a geologic map and sections, water-level-contour maps and profiles, and hydrographs of selected well. The Santa Ana River, the principal stream, flows generally westward across the area. Channels of the river and its tributaries overlie a large irregular structural depression filled with alluvial deposits ranging in age from late Tertiary to Recent and forming a valley bounded on the north by the San Gabriel Mountains, on the east by the San Bernardino Mountains, and on the south by an irregular group of hills. Large alluvial fans underlie most of the area, but its landforms also include alluvial benches and terraces near the mountains, stream channels, and elongate hills, ridges, and scarps along the trace of the San Jacinto fault, which strikes northwestward across the valley about in the center of the area. This fault and others divide the area into ground-water basins, which include the Bunker Hill, Rialto-Colton, upper and lower Lytle and Chino basins. The water-bearing deposits include the following units: the younger alluvium. of Recent age, which occupies principally the backfilled

  4. Characterization of high-fired PuO/sub 2/ as a certified reference material

    SciTech Connect

    Legeled, M.A.; Cacic, C.G.; Crawford, D.W.; Spaletto, M.I.

    1984-07-01

    The New Brunswick Laboratory (NBL), U.S. Department of Energy, has certified a plutonium dioxide reference material, CRM 122, for plutonium assay and isotopic composition. The PuO/sub 2/ standard, one of several certified Pu reference materials currently being developed at NBL for use in instrumentation calibration and measurement control for safeguards, establishes traceability to the national measurement base. This plutonium reference material in the oxide form provides more directly demonstrable traceability than metal because it undergoes the same chemical treatment for dissolution as PuO/sub 2/ fuel materials. Various tests for achieving a constant weight and for dissolving CRM 122 high-fired PuO/sub 2/ were conducted. Results of these tests as well as the certification data generated by controlled-potential coulometry for plutonium assay and by thermal ionization mass spectrometry for isotopic composition will also be presented and discussed.

  5. Water resources of southeastern Florida, with special reference to geology and ground water of the Miami area

    USGS Publications Warehouse

    Parker, Garald G.; Ferguson, G.E.; Love, S.K.

    1955-01-01

    The circulation of water, in any form, from the surface of the earth to the atmosphere and back again is called the hydrologic cycle. A comprehensive study of the water resources of any area must, therefore, include data on the climate of the area. The humid subtropical climate of southeast Florida is characterized by relatively high temperatures, alternating semi-annual wet and dry season, and usually light put persistent winds. The recurrence of drought in an area having relatively large rainfall such as southeastern Florida indicates that the agencies that remove water are especially effective. Two of the most important of the agencies associated with climate are evaporation and transpiration, or 'evapotranspiraton'. Evaporation losses from permanent water areas are believed to average between 40 and 45 inches per year. Over land areas indirect methods much be used to determine losses by evapotranspiration; necessarily, there values are not precise. Because of their importance in the occurrence and movement of both surface and ground waters, detailed studies were made of the geology and geomorphology of southern Florida. As a result of widespread crustal movements, southern Florida emerged from the sea in later Pliocene time and probably was slightly tilted to the west. At the beginning of the Pleistocene the continent emerged still farther as a result of the lowering of sea level attending the first widespread glaciation. During this epoch, south Florida may have stood several hundred feet above sea level. During the interglacial ages the sea repeatedly flooded southern Florida. The marine members of the Fort Thompson formation in the Lake Okeechobee-Everglades depression and the Calossahatchee River Valley apparently are the deposits of the interglacial invasions by the sea. The fresh-water marls, sands, and organic deposits of the Fort Thompson formation appear to have accumulated during glacial ages when seas level was low and the area was a land surface

  6. Atomic-absorption determination of beryllium in geological materials by use of electrothermal atomization

    USGS Publications Warehouse

    Campbell, E.Y.; Simon, F.O.

    1978-01-01

    A method is described for the atomic-absorption determination of beryllium in geological materials, that utilizes electrothermal atomization after a separation by solvent extraction. Samples are decomposed with hydrofluoric acid and nitric acid in Teflon-lined pressure decomposition vessels. Beryllium is isolated by its extraction as beryllium acetylacetonate at pH 8 into xylene and back-extraction in 3M hydrochloric acid. The method has been successfully applied to the determination of beryllium in 14 U.S. Geological Survey standard rocks. Four subsamples from four bottles of each standard sample were analysed in random order. The mean beryllium contents (ppm) are: AGV-1, 1.98; PCC-1, 0.024; MAG-1, 2.84; BHVO-1, 0.90; DTS-1, 0.026; SCo-1, 1.74; SDC-1, 2.52; BCR-1, 1.44; GSP-1, 1.22; SGR-1, 0.86; QLO-1, 1.83; RGM-1, 2.21; STM-1, 8.75; G-2, 2.29. An analysis of variance shows that all the samples may be considered homogeneous at F0.95 except AGV-1 and DTS-1 which may be considered homogeneous at F0.99. ?? 1978.

  7. Simulations of Fracture and Fragmentation of Geologic Materials using Combined FEM/DEM/SPH Analysis

    SciTech Connect

    Morris, J P; Johnson, S M

    2007-04-05

    An overview of the Lawrence Discrete Element Code (LDEC) is presented, and results from a study investigating the effect of explosive and impact loading on geologic materials using the Livermore Distinct Element Code (LDEC) are detailed. LDEC was initially developed to simulate tunnels and other structures in jointed rock masses using large numbers of polyhedral blocks. Many geophysical applications, such as projectile penetration into rock, concrete targets, and boulder fields, require a combination of continuum and discrete methods in order to predict the formation and interaction of the fragments produced. In an effort to model this class of problems, LDEC now includes implementations of Cosserat point theory and cohesive elements. This approach directly simulates the transition from continuum to discontinuum behavior, thereby allowing for dynamic fracture within a combined finite element/discrete element framework. In addition, a Smooth Particle Hydrodynamics (SPH) capability has been incorporated into LDEC, permitting the simulation of fluid-structure interaction. We will present results from a study of detonation-induced fracture and fragmentation of geologic media surrounding a tunnel using LDEC.

  8. Production of certified reference materials for the detection of genetically modified organisms.

    PubMed

    Trapmann, Stefanie; Schimmel, Heinz; Kramer, Gerard Nico; Van den Eede, Guy; Pauwels, Jean

    2002-01-01

    Certified reference materials (CRMs) are an essenIial tool in the quality assurance of analytical measurements. They are produced, certified, and used in accordance with relevant ISO (International Organization for Standardization) and BCR (Community Bureau of Reference) guidelines. The Institute for Reference Materials and Measurements (IRMM; Geel, Belgium) has produced the first powdery genetically modified organism (GMO) CRMs in cooperation with the Institute for Health and Consumer Protection (Ispra, Italy). Until now, different weight percentages in the range of 0-5% for 4 GMOs in Europe were produced and certified: Bt (Bacillus thuringiensis)-11 and Bt-176 maize, Roundup Ready soybean, and MON810 maize. Bt-11 and Bt-176 maize and Roundup Ready soybean were produced by IRMM on behalf of Fluka Chemie AG (Buchs, Switzerland). Characterization of used base material is the first step in production and is especially important for GMO CRMs. The production of powdery GMO CRMs and methods used for production control are described. Thorough control of homogeneity and stability are essential for certification of reference materials and ensure validity of the certificate for each bottle of a batch throughout a defined shelf-life. Because production of reference materials and their maintenance are very labor- and cost-intensive tasks, the usefulness of new types of GMO CRMs must be estimated carefully.

  9. Revised delta34S reference values for IAEA sulfur isotope reference materials S-2 and S-3.

    PubMed

    Mann, Jacqueline L; Vocke, Robert D; Kelly, W Robert

    2009-04-01

    Revised delta(34)S reference values with associated expanded uncertainties (95% confidence interval (C.I.)) are presented for the sulfur isotope reference materials IAEA-S-2 (22.62 +/- 0.16 per thousand) and IAEA-S-3 (-32.49 +/- 0.16 per thousand). These revised values are determined using two relative-difference measurement techniques, gas source isotope ratio mass spectrometry (GIRMS) and double-spike multi-collector thermal ionization mass spectrometry (MC-TIMS). Gas analyses have traditionally been considered the most robust for relative isotopic difference measurements of sulfur. The double-spike MC-TIMS technique provides an independent method for value-assignment validation and produces revised values that are both unbiased and more precise than previous value assignments. Unbiased delta(34)S values are required to anchor the positive and negative end members of the sulfur delta (delta) scale because they are the basis for reporting both delta(34)S values and the derived mass-independent Delta(33)S and Delta(36)S values.

  10. Microhomogeneity in reference materials for microanalytical methods - a possible recourse from a blind alley?

    NASA Astrophysics Data System (ADS)

    Renno, A. D.; Michalak, P. P.; Munnik, F.; Tolosana-Delgado, R.; van den Boogaart, G. K.

    2013-12-01

    It is assumed that reference materials for microanalytical methods must be homogeneous, i.e. have the same concentration of the relevant element(s) overall, to ensure that they can be used reliably to get comparison values during the analysis with non absolute methods. With increasing resolution it becomes more and more difficult to ensure such homogeneity, up to the point that it is not possible for several microanalytical methods. Painstaking search for homogeneous natural minerals in gem quality or elaborate expensive methods to produce synthetic minerals provide as obvious solutions to the problem. We propose a way to get reliable reference values with some types of inhomogeneous material, based on multiple probing the reference material. Consider a reference material, which average concentration on the relevant element and its microscale variability has been adequately characterized by a destructive method at a series of grid spots. The minimal number of probing spots required for a certain precision level can be derived from the variance calculations. This procedure is always valid, whenever the heterogeneity value distribution of the reference material has a variance, but at the price that the number of spots will be huge if it is large. However, using adequate models of local heterogeneity can greatly reduce that number. Geostatistics can be used in random, systematic and periodic heterogeneities, while robust methods are useful in cases of nugget heterogeneities. Typical examples of natural and synthetic minerals, analysed by electron microprobe and micro-PIXE (particle induced X-ray emission) for microhomogeneity/microheterogeneity are shown. The distinctions between the two strategies of using these materials as a potential reference material are demonstrated.

  11. Development of new reference materials for the determination of cadmium, chromium, mercury and lead in polycarbonate.

    PubMed

    Lee, Kil Jae; Lee, Yeo Jin; Choi, Young Rak; Kim, Jeong Sook; Kim, Youn Sung; Heo, Soo Bong

    2013-01-01

    Reference materials for quantitative determination of Cd, Cr, Hg and Pb in polycarbonate were developed. Reference materials with two concentration level of elements were prepared by adding appropriate amounts of chemicals to a blank polycarbonate base material. It was shown that ten bottles with triplicate analysis are enough to demonstrate the homogeneity of these candidate reference materials. The statistical results also showed no significant trends in both short-term stability test for four weeks and long-term stability test for twelve months. The certification of the four elements was carried out by isotope-dilution-inductively coupled plasma mass spectrometry (ID-ICP-MS) with microwave-assisted digestion. Certification of candidate reference materials in a single laboratory was confirmed with interlaboratory comparison participated by a certain number of well-recognized testing laboratories in Korea. The certified values and expanded uncertainties (k=2) for the candidate reference material with low level and the one with high level were (51.7±2.1)mgkg(-1) Cd, (103.8±2.9)mgkg(-1) Cd, (98.8±4.5)mgkg(-1) Cr, (1004±49.8)mgkg(-1) Cr, (107.4±4.6)mgkg(-1) Hg, (1133±50.7)mgkg(-1) Hg, (94.8±3.7)mgkg(-1) Pb and (988.4±53.6)mgkg(-1) Pb, respectively. The reference materials developed in this study demonstrated their suitability for the quality assurance in Cd, Cr, Hg and Pb analysis for the implementation of RoHS Directive. PMID:23245892

  12. Biological monitoring systems for hazardous waste sites (production and analysis of analytical reference materials)

    SciTech Connect

    Bohman, V.R.; Blincoe, C.R.; Miller, G.C.; Scholl, R.L.; Sutton, W.W.

    1989-02-01

    EPA programs in pesticides, toxics, and hazardous-waste require analytical reference materials. This project emphasized the collection of and analysis of urine, fat, and blood for ultimate use as reference samples and the practicality of using certain metabolites to indicate previous exposure to chlorinated hydrocarbons. The reference samples can, with verified compound concentrations, be used as qualifying samples when evaluating a technique to use for a particular analysis. However, the reference materials may be of greatest benefit when used by laboratories to determine analytical accuracy for samples of human urine, blood, etc. This is because the standards, like the unknown samples, will contain pollutant compounds and associated metabolites (all in vivo incorporated). Dairy animals were used during this study.

  13. Development of Reference Materials for Thermal-Diffusivity Measurements by the Flash Method

    NASA Astrophysics Data System (ADS)

    Akoshima, M.; Abe, H.; Baba, T.

    2015-12-01

    The thermal conductivity of solid materials used for thermal simulations and thermal designs can be obtained as the product of thermal diffusivity, specific heat capacity, and bulk density in many cases. The thermal diffusivity is usually measured by the flash method, and the specific heat capacity is usually measured by differential scanning calorimetry. In order to obtain reliable thermal conductivities for strict thermal design, it is necessary to measure the thermal diffusivity using the flash method, a well-validated apparatus. Reference materials are an effective means for validation of most practical measurement apparatus. For the flash method, isotropic graphite was selected as a candidate reference material. A batch of isotropic graphite samples was prepared and characterized in detail in order to be a certified reference material for thermal-diffusivity measurement. The detailed characterization ensures the traceability of the measurement results to the international system of units (SI). A convenient reference material for thermal conductivity was also obtained by using the known thermal-diffusivity measurements, specific heat capacity, and density of the material.

  14. Middle infrared spectral studies of geologic materials in their natural state using photothermal beam deflection spectroscopy

    NASA Astrophysics Data System (ADS)

    Eastes, J. W.; Low, M. J. D.

    1984-04-01

    The use of a novel laboratory spectral technique is described for the recording of middle infrared (MIR) absorption spectra of natural surfaces with no sample preparation. Such a technique allows evaluation of spectral influences of surficial films such as weathering products, lichen cover or desert varnish on the spectra of the substrate geologic materials. In remote sensing applications the technique should provide spectral information more nearly representative of field conditions and may improve interpretation of thermal imagery. The technique, called photothermal beam deflection spectroscopy (PBDS) was originally developed for studies of surface chemistry in situations where it is impractical or impossible to separate surface layers from their substrate. In the present studies the spectral characteristics of natural rock and mineral surfaces have been examined.

  15. An atomic-absorption method for the determination of gold in large samples of geologic materials

    USGS Publications Warehouse

    VanSickle, Gordon H.; Lakin, Hubert William

    1968-01-01

    A laboratory method for the determination of gold in large (100-gram) samples has been developed for use in the study of the gold content of placer deposits and of trace amounts of gold in other geologic materials. In this method the sample is digested with bromine and ethyl ether, the gold is extracted into methyl isobutyl ketone, and the determination is made by atomicabsorption spectrophotometry. The lower limit of detection is 0.005 part per million in the sample. The few data obtained so far by this method agree favorably with those obtained by assay and by other atomic-absorption methods. About 25 determinations can be made per man-day.

  16. Determination of gold in geologic materials by solvent extraction and atomic-absorption spectrometry

    USGS Publications Warehouse

    Huffman, Claude; Mensik, J.D.; Riley, L.B.

    1967-01-01

    The two methods presented for the determination of traces of gold in geologic materials are the cyanide atomic-absorption method and the fire-assay atomic-absorption method. In the cyanide method gold is leached with a sodium-cyanide solution. The monovalent gold is then oxidized to the trivalent state and concentrated by extracting into methyl isobutyl ketone prior to estimation by atomic absorption. In the fire-assay atomic-absorption method, the gold-silver bead obtained from fire assay is dissolved in nitric and hydrochloric acids. Gold is then concentrated by extracting into methyl isobutyl ketone prior to determination by atomic absorption. By either method concentrations as low as 50 parts per billion of gold can be determined in a 15-gram sample.

  17. CD Reference Materials Fabricated on Monolithic 200 mm Wafers for Automated Metrology Tool Applications

    NASA Astrophysics Data System (ADS)

    Allen, Richard A.; Dixson, Ronald G.; Cresswell, Michael W.; Guthrie, William F.; Shulver, Byron J. R.; Bunting, A. S.; Stevenson, J. T. M.; Walton, Anthony J.

    2007-09-01

    Recently, prototype isolated-line, single-crystal critical dimension (CD) reference materials (SCCDRMs) with linewidths as narrow as 40 nm±1.5 nm have been reported. These reference materials, designated NIST Prototype Reference Material (RM) 8111, were configured as 10 mm by 11 mm silicon test chips mounted in 200 mm carrier wafers. The RM 8111 chips were fabricated using microelectromechanical (MEMS) process techniques, which assure the alignment of the sidewalls of the features to silicon (111) lattice planes, and were calibrated in a sequence involving atomic force microscopy (AFM) and high resolution transmission electron microscopy (HRTEM) metrology. This paper reports initial results on SCCDRMs fabricated on 200 mm bulk wafers; this monolithic approach would eliminate the need for carrier wafers.

  18. Laser-Based Dynamic Compression of Geological Materials to Ultrahigh Pressures

    NASA Astrophysics Data System (ADS)

    Duffy, T. S.

    2015-12-01

    Laser-based dynamic compression provides new opportunities to study the structures and properties of geological materials to ultrahigh pressure conditions reaching 1 terapascal and beyond. By controlling the shape and duration of the incident laser pulse, either shock or ramp (shockless) loading can be produced. Samples can be compressed for ~10s of nanoseconds on spatial scales of ~1 millimeter. Diagnostics include velocity interferometry from which the stress-density response of the material can be determined and X-ray diffraction from which lattice-level structural information is obtained. Our experiments are being carried out at a suite of facilities including the Omega Laser (U. of Rochester), Linear Coherent Light Source (LCLS), and National Ignition Facility (Livermore). Using ramp compression we have constrained pressure-density states in a variety of materials including iron, magnesium oxide, and carbon. X-ray diffraction has been used as a diagnostic to probe the B1-B2 phase transition in MgO under both ramp and shock loading to multi-megabar pressures. We have also examined this same phase transition at more modest pressures on sodium chloride at the LCLS, observing both the B1-B2 transition upon compression and its back transformation upon release. X-ray diffraction measurements have also been used to study the melting curves and high-pressure phase stability of transition metals and alloys, including compositions relevant to the cores of Earth and super-Earth planets.

  19. Using U.S. Geological Survey data in material flow analysis: An introduction

    USGS Publications Warehouse

    Sibley, S.F.

    2009-01-01

    A few sources of basic data on worldwide raw materials production and consumption exist that are independently developed and freely available to the public. This column is an introduction to the types of information available from the U.S. Geological Survey (USGS), and explains how the data are assembled. The kind of information prepared by the USGS is essential to U.S. materials flow studies because the data make it possible to conduct these studies within a global context. The data include primary and secondary (scrap) production, consumption and stocks (mostly limited to the United States unless calculated), trade (not readily available for all countries), and prices for more than 80 mineral commodities. Materials flow studies by USGS specialists using these data are continuing (http://minerals.usgs.gov/minerals/mflow/). Figure 1 shows from where the data are collected and where they are used. Minerals information was downloaded by users 5.8 million times from USGS minerals information Web pages in 2008.

  20. Determination of rare earth elements in geological materials by inductively coupled argon plasma/atomic emission spectrometry

    USGS Publications Warehouse

    Crock, J.G.; Lichte, F.E.

    1982-01-01

    Inductively coupled argon plasma/optical emission spectrometery (ICAP/OES) is useful as a simultaneous, multielement analytical technique for the determination of trace elements in geological materials. A method for the determination of trace-level rare earth elements (REE) in geological materials using an ICAP 63-channel emission spectrometer is described. Separation and preconcentration of the REE and yttrium from a sample digest are achieved by a nitric acid gradient cation exchange and hydrochloric acid anion exchange. Precision of 1-4% relative standard deviation and comparable accuracy are demonstrated by the triplicate analysis of three splits of BCR-1 and BHVO-1. Analyses of other geological materials including coals, soils, and rocks show comparable precision and accuracy.

  1. Reference materials and representative test materials to develop nanoparticle characterization methods: the NanoChOp project case

    NASA Astrophysics Data System (ADS)

    Roebben, Gert; Kestens, Vikram; Varga, Zoltan; Charoud-Got, Jean; Ramaye, Yannic; Gollwitzer, Christian; Bartczak, Dorota; Geißler, Daniel; Noble, James; Mazoua, Stéphane; Meeus, Nele; Corbisier, Philippe; Palmai, Marcell; Mihály, Judith; Krumrey, Michael; Davies, Julie; Resch-Genger, Ute; Kumarswami, Neelam; Minelli, Caterina; Sikora, Aneta; Goenaga-Infante, Heidi

    2015-10-01

    This paper describes the production and characteristics of the nanoparticle test materials prepared for common use in the collaborative research project NanoChOp (Chemical and optical characterisation of nanomaterials in biological systems), in casu suspensions of silica nanoparticles and CdSe/CdS/ZnS quantum dots. This paper is the first to illustrate how to assess whether nanoparticle test materials meet the requirements of a 'reference material' (ISO Guide 30:2015) or rather those of the recently defined category of 'representative test material' (ISO TS 16195:2013). The NanoChOp test materials were investigated with small-angle X-ray scattering (SAXS), dynamic light scattering (DLS) and centrifugal liquid sedimentation (CLS) to establish whether they complied with the required monomodal particle size distribution. The presence of impurities, aggregates, agglomerates and viable microorganisms in the suspensions was investigated with DLS, CLS, optical and electron microscopy and via plating on nutrient agar. Suitability of surface functionalization was investigated with attenuated total reflection Fourier transform infrared spectrometry (ATR-FTIR) and via the capacity of the nanoparticles to be fluorescently labeled or to bind antibodies. Between-unit homogeneity and stability were investigated in terms of particle size and zeta potential. This paper shows that only based on the outcome of a detailed characterization process one can raise the status of a test material to representative test material or reference material, and how this status depends on its intended use.

  2. U.S. Geological Survey Field Leach Test for Assessing Water Reactivity and Leaching Potential of Mine Wastes, Soils, and Other Geologic and Environmental Materials

    USGS Publications Warehouse

    Hageman, Philip L.

    2007-01-01

    The U. S. Geological Survey (USGS) has developed a fast (5-minute), effective, simple, and cost-effective leach test that can be used to simulate the reactions that occur when materials are leached by water. The USGS Field Leach Test has been used to predict, assess, and characterize the geochemical interactions between water and a broad variety of geologic and environmental matrices. Examples of some of the samples leached include metal mine wastes, various types of dusts, biosolids (processed sewage sludge), flood and wetland sediments, volcanic ash, forest-fire burned soils, and many other diverse matrices. The Field Leach Test has been an integral part of these investigations and has demonstrated its value as a geochemical characterization tool. It has enabled investigators to identify which constituents are water reactive, soluble, mobilized, and made bioaccessible because of leaching by water, and to understand potential impacts of these interactions on the surrounding environment.

  3. Development and Characterization of Reference Materials for Genetic Testing: Focus on Public Partnerships.

    PubMed

    Kalman, Lisa V; Datta, Vivekananda; Williams, Mickey; Zook, Justin M; Salit, Marc L; Han, Jin Yeong

    2016-11-01

    Characterized reference materials (RMs) are needed for clinical laboratory test development and validation, quality control procedures, and proficiency testing to assure their quality. In this article, we review the development and characterization of RMs for clinical molecular genetic tests. We describe various types of RMs and how to access and utilize them, especially focusing on the Genetic Testing Reference Materials Coordination Program (Get-RM) and the Genome in a Bottle (GIAB) Consortium. This review also reinforces the need for collaborative efforts in the clinical genetic testing community to develop additional RMs.

  4. Development and Characterization of Reference Materials for Genetic Testing: Focus on Public Partnerships.

    PubMed

    Kalman, Lisa V; Datta, Vivekananda; Williams, Mickey; Zook, Justin M; Salit, Marc L; Han, Jin Yeong

    2016-11-01

    Characterized reference materials (RMs) are needed for clinical laboratory test development and validation, quality control procedures, and proficiency testing to assure their quality. In this article, we review the development and characterization of RMs for clinical molecular genetic tests. We describe various types of RMs and how to access and utilize them, especially focusing on the Genetic Testing Reference Materials Coordination Program (Get-RM) and the Genome in a Bottle (GIAB) Consortium. This review also reinforces the need for collaborative efforts in the clinical genetic testing community to develop additional RMs. PMID:27578503

  5. Molecular diagnostics: harmonization through reference materials, documentary standards and proficiency testing.

    PubMed

    Holden, Marcia J; Madej, Roberta M; Minor, Philip; Kalman, Lisa V

    2011-09-01

    There is a great need for harmonization in nucleic acid testing for infectious disease and clinical genetics. The proliferation of assay methods, the number of targets for molecular diagnostics and the absence of standard reference materials contribute to variability in test results among laboratories. This article provides a comprehensive overview of reference materials, related documentary standards and proficiency testing programs. The article explores the relationships among these resources and provides necessary information for people practicing in this area that is not taught in formal courses and frequently is obtained on an ad hoc basis. The aim of this article is to provide helpful tools for molecular diagnostic laboratories.

  6. Evaluation of homogeneity of a certified reference material by instrumental neutron activation analysis

    SciTech Connect

    Kratochvil, B.; Duke, M.J.M.; Ng, D.

    1986-01-01

    The homogeneity of the marine reference material TORT-1, a spray-dried and acetone-extracted hepatopancreatic material from the lobster, was tested for 26 elements by instrumental neutron activation analysis (INAA). Through a one-way analysis of variance based on six analyses on each of six bottles of TORT-1, it was concluded that the between-bottle heterogeneity is no greater than the within-bottle heterogeneity. The analytical results for those elements for which values were provided by NRC agree with the NRC values within 95% confidence limits. 8 references, 6 tables.

  7. Development and Characterization of Reference Materials for Genetic Testing: Focus on Public Partnerships

    PubMed Central

    Kalman, Lisa V.; Datta, Vivekananda; Williams, Mickey; Zook, Justin M.; Salit, Marc L.

    2016-01-01

    Characterized reference materials (RMs) are needed for clinical laboratory test development and validation, quality control procedures, and proficiency testing to assure their quality. In this article, we review the development and characterization of RMs for clinical molecular genetic tests. We describe various types of RMs and how to access and utilize them, especially focusing on the Genetic Testing Reference Materials Coordination Program (Get-RM) and the Genome in a Bottle (GIAB) Consortium. This review also reinforces the need for collaborative efforts in the clinical genetic testing community to develop additional RMs. PMID:27578503

  8. Determination of sub-microgram amounts of selenium in geological materials by atomic-absorption spectrophotometry with electrothermal atomisation after solvent extraction

    USGS Publications Warehouse

    Sanzolone, R.F.; Chao, T.T.

    1981-01-01

    An atomic-absorption spectrophotometric method with electrothermal atomisation has been developed for the determination of selenium in geological materials. The sample is decomposed with a mixture of nitric, perchloric and hydrofluoric acids and heated with hydrochloric acid to reduce selenium to selenium (IV). Selenium is then extracted into toluene from a hydrochloric acid - hydrobromic acid medium containing iron. A few microlitres of the toluene extract are injected into a carbon rod atomiser, using a nickel solution as a matrix modifier. The limits of determination are 0.2-200 p.p.m. of selenium in a geological sample. For concentrations between 0.05 and 0.2 p.p.m., back-extraction of the selenium into dilute hydrochloric acid is employed before atomisation. Selenium values for reference samples obtained by replicate analysis are in general agreement with those reported by other workers, with relative standard deviations ranging from 4.1 to 8.8%. Recoveries of selenium spiked at two levels were 98-108%. Major and trace elements commonly encountered in geological materials do not interfere. Arsenic has a suppressing effect on the selenium signals, but only when its concentration is greater than 1000 p.p.m. Nitric acid interferes seriously with the extraction of selenium and must be removed by evaporation in the sample-digestion step.

  9. Assessment of international reference materials for isotope-ratio analysis (IUPAC Technical Report)

    USGS Publications Warehouse

    Brand, Willi A.; Coplen, Tyler B.; Vogl, Jochen; Rosner, Martin; Prohaska, Thomas

    2014-01-01

    Since the early 1950s, the number of international measurement standards for anchoring stable isotope delta scales has mushroomed from 3 to more than 30, expanding to more than 25 chemical elements. With the development of new instrumentation, along with new and improved measurement procedures for studying naturally occurring isotopic abundance variations in natural and technical samples, the number of internationally distributed, secondary isotopic reference materials with a specified delta value has blossomed in the last six decades to more than 150 materials. More than half of these isotopic reference materials were produced for isotope-delta measurements of seven elements: H, Li, B, C, N, O, and S. The number of isotopic reference materials for other, heavier elements has grown considerably over the last decade. Nevertheless, even primary international measurement standards for isotope-delta measurements are still needed for some elements, including Mg, Fe, Te, Sb, Mo, and Ge. It is recommended that authors publish the delta values of internationally distributed, secondary isotopic reference materials that were used for anchoring their measurement results to the respective primary stable isotope scale.

  10. Development and certification of green tea-containing standard reference materials.

    PubMed

    Sander, L C; Bedner, M; Tims, M C; Yen, J H; Duewer, D L; Porter, B; Christopher, S J; Day, R D; Long, S E; Molloy, J L; Murphy, K E; Lang, B E; Lieberman, R; Wood, L J; Payne, M J; Roman, M C; Betz, J M; NguyenPho, A; Sharpless, K E; Wise, S A

    2012-01-01

    A suite of three green tea-containing Standard Reference Materials (SRMs) has been issued by the National Institute of Standards and Technology (NIST): SRM 3254 Camellia sinensis (Green Tea) Leaves, SRM 3255 Camellia sinensis (Green Tea) Extract, and SRM 3256 Green Tea-Containing Solid Oral Dosage Form. The materials are characterized for catechins, xanthine alkaloids, theanine, and toxic elements. As many as five methods were used in assigning certified and reference values to the constituents, with measurements carried out at NIST and at collaborating laboratories. The materials are intended for use in the development and validation of new analytical methods, and for use as control materials as a component in the support of claims of metrological traceability. PMID:22127575

  11. Using Photon Activation Analysis To Determine Concentrations Of Unknown Components In Reference Materials

    SciTech Connect

    Green, Jaromy; Sun, Zaijing; Wells, Doug; Maschner, Herb

    2011-06-01

    Using certified multi-element reference materials for instrumental analyses one frequently is confronted with the embarrassing fact that the concentration of some desired elements are not given in the respective certificate, nonetheless are detectable, e.g. by photon activation analysis (PAA). However, these elements might be determinable with sufficient quality of the results using scaling parameters and the well-known quantities of a reference element within the reference material itself. Scaling parameters include: activation threshold energy, Giant Dipole Resonance (GDR) peak and endpoint energy of the bremsstrahlung continuum; integrated photo-nuclear cross sections for the isotopes of the reference element; bremsstrahlung continuum integral; target thickness; photon flux density. Photo-nuclear cross sections from the unreferenced elements must be known, too. With these quantities, the integral was obtained for both the known and unknown elements resulting in an inference of the concentration of the unreported element based upon the reported value, thus also the concentration of the unreferenced element in the reference material. A similar method to determine elements using the basic nuclear and experimental data has been developed for thermal neutron activation analysis some time ago (k{sub 0} Method).

  12. Homogeneity study of a corn flour laboratory reference material candidate for inorganic analysis.

    PubMed

    Dos Santos, Ana Maria Pinto; Dos Santos, Liz Oliveira; Brandao, Geovani Cardoso; Leao, Danilo Junqueira; Bernedo, Alfredo Victor Bellido; Lopes, Ricardo Tadeu; Lemos, Valfredo Azevedo

    2015-07-01

    In this work, a homogeneity study of a corn flour reference material candidate for inorganic analysis is presented. Seven kilograms of corn flour were used to prepare the material, which was distributed among 100 bottles. The elements Ca, K, Mg, P, Zn, Cu, Fe, Mn and Mo were quantified by inductively coupled plasma optical emission spectrometry (ICP OES) after acid digestion procedure. The method accuracy was confirmed by analyzing the rice flour certified reference material, NIST 1568a. All results were evaluated by analysis of variance (ANOVA) and principal component analysis (PCA). In the study, a sample mass of 400mg was established as the minimum mass required for analysis, according to the PCA. The between-bottle test was performed by analyzing 9 bottles of the material. Subsamples of a single bottle were analyzed for the within-bottle test. No significant differences were observed for the results obtained through the application of both statistical methods. This fact demonstrates that the material is homogeneous for use as a laboratory reference material.

  13. PAHs in baby food: assessment of three different processing techniques for the preparation of reference materials.

    PubMed

    Huertas-Pérez, José Fernando; Bordajandi, Luisa R; Sejerøe-Olsen, Berit; Emteborg, Håkan; Baù, Andrea; Schimmel, Heinz; Dabrio, Marta

    2015-04-01

    A feasibility study for producing a matrix reference material for selected polycyclic aromatic hydrocarbons (PAHs) in baby food is reported. A commercially available baby food, containing carrots, potatoes, tomato, white beans and meat, was spiked with the so-called 15 + 1 PAHs included in the PAHs priority list for food of the EU, at a mass fraction level of 1 μg/kg. The contaminated baby food was further processed by autoclaving, freezing or freeze drying. The homogeneity of the three materials (bottle-to-bottle variation) and their short-term (4 weeks) and long-term (18 months) stability at different temperatures were assessed. To this end, an analytical method based on a solid-liquid extraction followed by cleaning up with gel permeation chromatography (GPC) and solid phase extraction (SPE) and GC-IDMS determination, was validated in-house. It could be demonstrated that the procedure fulfilled the demands for application to the homogeneity and isochronous stability studies for the candidate reference materials targeted here. All three materials proved to be sufficiently homogeneous for the intended use. Measurements on the autoclaved material provided the most promising results in terms of envisaged shelf life, although freeze drying was also found to be a suitable processing technique for most of the investigated PAHs. These results are an important step towards the development of a matrix reference material for PAHs in a processed food matrix in a presentation very similar to routine samples.

  14. Application of the Bammann inelasticity internal state variable constitutive model to geological materials

    NASA Astrophysics Data System (ADS)

    Sherburn, J. A.; Horstemeyer, M. F.; Bammann, D. J.; Baumgardner, J. R.

    2011-03-01

    We describe how the Bammann internal state variable (ISV) constitutive approach, which has proven highly successful in modelling deformation processes in metals, can be applied with great benefit to silicate rocks and other geological materials in modelling their deformation dynamics. In its essence, ISV theory provides a constitutive framework to account for changing history states that arise from inelastic dissipative microstructural evolution of a polycrystalline solid. In this paper, we restrict our attention to a Bammann ISV elastic-viscoplastic model with temperature and strain rate dependence and use isotropic hardening and anisotropic hardening as our two ISVs. We show the Bammann model captures the inelastic behaviour of olivine aggregates (with and without water), lherzolite (with and without water), Carrara marble and rock salt using some experimental data found in the literature. These examples illustrate that when more experimental stress-strain data are gathered on other rock materials, much more realistic numerical simulation of rock behaviour becomes feasible. Though not available in the literature, we outline a set of experiments to obtain unique Bammann ISV model constants.

  15. Development of a mushroom powder Certified Reference Material for calcium, arsenic, cadmium and lead measurements.

    PubMed

    Chew, Gina; Sim, Lay Peng; Ng, Sin Yee; Ding, Yi; Shin, Richard Y C; Lee, Tong Kooi

    2016-01-01

    Isotope dilution mass spectrometry and standard addition techniques were developed for the analysis of four elements (Ca, As, Cd and Pb) in a mushroom powder material. Results from the validated methods were compared to those of other national metrology institutes in the CCQM-K89 intercomparisons and the results were in excellent agreement with the reference values. The same methods were then used for the assignment of reference values to a mushroom powder Certified Reference Material (CRM). The certified values obtained for Ca, As, Cd and Pb were 1.444 ± 0.099 mg/g, 5.61 ± 0.59 mg/kg, 1.191 ± 0.079 mg/kg and 5.23 ± 0.94 mg/kg, respectively. The expanded measurement uncertainties were obtained by combining the uncertainty contributions from characterization (uchar) and between-bottle homogeneity (ubb).

  16. Analysis of marine sediment and lobster hepatopancreas reference materials by instrumental photon activation

    SciTech Connect

    Landsberger, S.; Davidson, W.F.

    1985-01-01

    By use of instrumental photon activation analysis, twelve trace (As, Ba, Cr, Co, Mn, Ni, Pb, Sb, Sr, U, Zn, and Zr) and eight minor (C, Na, Mg, Co, K, Ca, Tl, and Fe) elements were determined in a certified marine sediment standard reference material as well as eight trace (Mn, Ni, Cu, Zn, As, Sr, Cd, and Pb) and four minor (Na, Mg, Cl, and Ca) elements in a certified marine tissue (lobster hepatopancreas) standard reference material. The precision and accuracy of the present results when compared to the accepted values clearly demonstrate the reliability of this nondestructive technique and its applicability to marine environmental or marine geochemical studies. 24 references, 4 figures, 3 tables.

  17. Reference Materials for Food and Nutrition Metrology: Past, Present and Future

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Establishment of a metrology-based measurement system requires the solid foundation of traceability of measurements to available, appropriate certified reference materials (CRM). In the early 1970’s the first “biological” RM of Bowens Kale, as well as Orchard Leaves and Bovine Liver SRMs, from the ...

  18. 40 CFR 1045.810 - What materials does this part reference?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... Register approved the incorporation by reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone... Administration (NARA). For information on the availability of this material at NARA, call 202-741-6030, or go...

  19. Sources of Braille Reading Materials. Reference Circular No. 86-2.

    ERIC Educational Resources Information Center

    Redmond, Linda, Comp.

    This reference circular lists sources of braille books available for loan, purchase, rental, or free (give-away) distribution. Divided into four sections, it includes general sources of braille books, sources of specialized braille materials, the major braille presses, and resources for further information about braille books and magazines.…

  20. 40 CFR 1048.810 - What materials does this part reference?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... Register approved the incorporation by reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone..., Switzerland or http://www.iso.org. Table 2 follows: Table 2 of § 1048.810—ISO Materials Document number...

  1. 40 CFR 1048.810 - What materials does this part reference?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... Register approved the incorporation by reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone..., Switzerland or http://www.iso.org. Table 2 follows: Table 2 of § 1048.810—ISO Materials Document number...

  2. 40 CFR 1048.810 - What materials does this part reference?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Register approved the incorporation by reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone..., Switzerland or http://www.iso.org. Table 2 follows: Table 2 of § 1048.810—ISO Materials Document number...

  3. New matrix-free reference material for ethene in the form of optical fibres.

    PubMed

    Słomińska, Marta; Konieczka, Piotr; Namieśnik, Jacek

    2013-02-01

    Reference materials are indispensable in the quality control and quality assurance of analytical measurements. One novel approach to the generation of standard gaseous mixtures of toxic, reactive, volatile, labile, and malodorous substances involves thermal decomposition or rearrangement, under defined temperature conditions, of compounds immobilized, by chemical bonding, on the surface of an appropriate carrier to release specific amounts of a volatile compound. In this technique the type of support used to immobilize the compound is extremely important, because the amount of analyte released depends directly on the choice of material. In this paper we report the novel preparation of a matrix-free ethene standard in the form of glass fibres coated with a thin layer of aluminium, the surface of which is modified by reaction with a specific compound. As a result of thermal decomposition of this compound, gaseous ethene is formed. In this paper we present the results obtained from tests of stability and homogeneity, two properties of crucial importance in the preparation of reference materials, by comparison of a series of results obtained for randomly chosen samples of the reference material. Interlaboratory comparative studies resulted in determination of a reference value for the ethene formed after thermal decomposition of the surface compound ((2.12 ± 0.14) ng per fibre). PMID:23239177

  4. Doorways III: Teacher Reference Materials. On School-Related Gender-Based Violence Prevention and Response

    ERIC Educational Resources Information Center

    US Agency for International Development, 2009

    2009-01-01

    The Doorways training program was designed by the U.S. Agency for International Development (USAID)-funded Safe Schools Program (Safe Schools) to enable teachers, community members and students to prevent and respond to school-related gender-based violence (SRGBV). This booklet, "Doorways III: Teacher Reference Materials on School-Related…

  5. 40 CFR 1068.95 - What materials does this part reference?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... reference as prescribed in 5 U.S.C. 552(a) and 1 CFR part 51. Anyone may inspect copies at the U.S. EPA, Air.../code_of_federal_regulations/ibr_locations.html. (a) SAE material. Table 1 to this section lists... Commonwealth Drive, Warrendale, PA 15096 or http://www.sae.org. Table 1 follows: Table 1 to §...

  6. Development of a new cucumber reference material for pesticide residue analysis: feasibility study for material processing, homogeneity and stability assessment.

    PubMed

    Grimalt, Susana; Harbeck, Stefan; Shegunova, Penka; Seghers, John; Sejerøe-Olsen, Berit; Emteborg, Håkan; Dabrio, Marta

    2015-04-01

    The feasibility of the production of a reference material for pesticide residue analysis in a cucumber matrix was investigated. Cucumber was spiked at 0.075 mg/kg with each of the 15 selected pesticides (acetamiprid, azoxystrobin, carbendazim, chlorpyrifos, cypermethrin, diazinon, (α + β)-endosulfan, fenitrothion, imazalil, imidacloprid, iprodione, malathion, methomyl, tebuconazole and thiabendazole) respectively. Three different strategies were considered for processing the material, based on the physicochemical properties of the vegetable and the target pesticides. As a result, a frozen spiked slurry of fresh cucumber, a spiked freeze-dried cucumber powder and a freeze-dried cucumber powder spiked by spraying the powder were studied. The effects of processing and aspects related to the reconstitution of the material were evaluated by monitoring the pesticide levels in the three materials. Two separate analytical methods based on LC-MS/MS and GC-MS/MS were developed and validated in-house. The spiked freeze-dried cucumber powder was selected as the most feasible material and more exhaustive studies on homogeneity and stability of the pesticide residues in the matrix were carried out. The results suggested that the between-unit homogeneity was satisfactory with a sample intake of dried material as low as 0.1 g. A 9-week isochronous stability study was undertaken at -20 °C, 4 °C and 18 °C, with -70 °C designated as the reference temperature. The pesticides tested exhibited adequate stability at -20 °C during the 9-week period as well as at -70 °C for a period of 18 months. These results constitute a good basis for the development of a new candidate reference material for selected pesticides in a cucumber matrix. PMID:25627789

  7. Reference materials and representative test materials to develop nanoparticle characterization methods: the NanoChOp project case

    PubMed Central

    Roebben, Gert; Kestens, Vikram; Varga, Zoltan; Charoud-Got, Jean; Ramaye, Yannic; Gollwitzer, Christian; Bartczak, Dorota; Geißler, Daniel; Noble, James; Mazoua, Stephane; Meeus, Nele; Corbisier, Philippe; Palmai, Marcell; Mihály, Judith; Krumrey, Michael; Davies, Julie; Resch-Genger, Ute; Kumarswami, Neelam; Minelli, Caterina; Sikora, Aneta; Goenaga-Infante, Heidi

    2015-01-01

    This paper describes the production and characteristics of the nanoparticle test materials prepared for common use in the collaborative research project NanoChOp (Chemical and optical characterization of nanomaterials in biological systems), in casu suspensions of silica nanoparticles and CdSe/CdS/ZnS quantum dots (QDs). This paper is the first to illustrate how to assess whether nanoparticle test materials meet the requirements of a “reference material” (ISO Guide 30, 2015) or rather those of the recently defined category of “representative test material (RTM)” (ISO/TS 16195, 2013). The NanoChOp test materials were investigated with small-angle X-ray scattering (SAXS), dynamic light scattering (DLS), and centrifugal liquid sedimentation (CLS) to establish whether they complied with the required monomodal particle size distribution. The presence of impurities, aggregates, agglomerates, and viable microorganisms in the suspensions was investigated with DLS, CLS, optical and electron microscopy and via plating on nutrient agar. Suitability of surface functionalization was investigated with attenuated total reflection Fourier transform infrared spectrometry (ATR-FTIR) and via the capacity of the nanoparticles to be fluorescently labeled or to bind antibodies. Between-unit homogeneity and stability were investigated in terms of particle size and zeta potential. This paper shows that only based on the outcome of a detailed characterization process one can raise the status of a test material to RTM or reference material, and how this status depends on its intended use. PMID:26539428

  8. Matrix effects on the determination of manganese in geological materials by atomic-absorption spectrophotometry under different flame conditions

    USGS Publications Warehouse

    Sanzolone, R.F.; Chao, T.T.

    1978-01-01

    Suppression caused by five of the seven matrix elements studied (Si, Al, Fe, Ca and Mg) was observed in the atomic-absorption determination of manganese in geological materials, when synthetic solutions and the recommended oxidizing air-acetylene flame were used. The magnitude of the suppression effects depends on (1) the kind and concentration of the interfering elements, (2) the type of acid medium, and (3) the concentration of manganese to be determined. All interferences noted are removed or alleviated by using a reducing nitrous oxide-acetylene flame. The atomic-absorption method using this flame can be applied to the determination of total and extractable manganese in a wide range of geological materials without interferences. Analyses of six U.S. Geological Survey rock standards for manganese gave results in agreement with the reported values. ?? 1978.

  9. Characterization of the Defense Waste Processing Facility (DWPF) Environmental Assessment (EA) glass standard reference material. [Site Characterization

    SciTech Connect

    Jantzen, C.M.; Bibler, N.E.; Beam, D.C.

    1992-09-30

    Liquid high-level nuclear waste at the Savannah River Site (SRS) will be immobilized by vitrification in borosilicate glass. The glass will be produced and poured into stainless steel canisters in the Defense Waste Processing Facility (DWPF). Other waste form producers, such as West Valley Nuclear Services (WVNS) and the Hanford Waste Vitrification Project (HWVP), will also immobilize high-level radioactive waste in borosilicate glass. The canistered waste will be stored temporarily at each facility for eventual permanent disposal in a geologic repository. The Department of Energy has defined a set of requirements for the canistered waste forms, the Waste Acceptance Preliminary Specifications (WAPS). The current Waste Acceptance Preliminary Specification (WAPS) 1.3, the product consistency specification, requires the waste form producers to demonstrate control of the consistency of the final waste form using a crushed glass durability test, the Product Consistency Test (PCT). In order to be acceptable, a waste glass must be more durable during PCT analysis than the waste glass identified in the DWPF Envirorunental Assessment (EA). In order to supply all the waste form producers with the same standard benchmark glass, 1000 pounds of the EA glass was fabricated. The chemical analyses and characterization of the benchmark EA glass are reported. This material is now available to act as a durability, analytic, and/or redox Standard Reference Material (SRM) for all waste form producers.

  10. Measurements of plutonium, 237Np, and 137Cs in the BCR 482 lichen reference material

    DOE PAGESBeta

    Lavelle, Kevin B.; Miller, Jeffrey L.; Hanson, Susan K.; Connick, William B.; Spitz, Henry B.; Glover, Samuel E.; Oldham, Warren J.

    2015-10-01

    Select anthropogenic radionuclides were measured in lichen reference material, BCR 482. This material was originally collected in Axalp, Switzerland in 1991 and is composed of the epiphytic lichen Pseudevernia furfuracea. Samples from three separate bottles of BCR 482 were analyzed for uranium, neptunium, and plutonium isotopes by inductively coupled plasma mass spectrometry (ICP-MS) and analyzed for cesium-137 by gamma-ray spectrometry. The isotopic composition of the radionuclides measured in BCR 482 suggests contributions from both global fallout resulting from historical nuclear weapons testing and more volatile materials released following the Chernobyl accident.

  11. Polychlorinated biphenyls (PCB), chlorinated pesticides, and polycyclic aromatic hydrocarbons (PAHs) in environmental standard reference materials

    SciTech Connect

    Poster, D.L.; Schantz, M.M.; Parris, R.M.; Benner, B.A. Jr.; Wise, S.A.

    1995-12-31

    Standard reference materials (SRMs) are certified reference materials issued by the National Institute of Standards and Technology (NIST). Natural matrix environmental sample SRMs have been developed the Analytical Chemistry Division to assist in validating measurements for organic contaminants in the environment. Many of these are well characterized for contaminants such as polychlorinated biphenyls (PCBs), chlorinated pesticides, and polycyclic aromatic hydrocarbons (PAHs). SRM 1649, Organics in Urban Dust, is currently available with certified concentrations for 5 PAHs but because of the widespread use of this material in air pollution monitoring programs and to expand the usefulness of this material, the authors are further characterizing the material for a larger number of PAHs as well as PCBs and chlorinated pesticides. They will also soon issue a diesel particulate extract (SRM 1975) that is well characterized for PAHS, including many nitrogen substituted compounds. In addition to natural matrix materials, solutions useful for calibrating chromatographic detector response factors and retention times, and spiking sample blanks for determination of analyte recoveries, are also available. Solution SRMs currently available contain PCS congeners, chlorinated pesticides, and PAHs. New solution SRMs in preparation will contain additional chlorinated pesticides, PCB congeners (e.g., non-ortho substituted chlorobiphenyls), and perdeuterated PAHs. Recent SRM work will be presented with particular attention on the methods used for determining organic contaminant concentrations in the urban dust material and in the diesel particulate extract.

  12. 10 CFR 51.109 - Public hearings in proceedings for issuance of materials license with respect to a geologic...

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 10 Energy 2 2010-01-01 2010-01-01 false Public hearings in proceedings for issuance of materials license with respect to a geologic repository. 51.109 Section 51.109 Energy NUCLEAR REGULATORY COMMISSION... (including any supplement thereto) prepared by the Secretary of Energy. If the position of the staff is...

  13. 10 CFR 51.109 - Public hearings in proceedings for issuance of materials license with respect to a geologic...

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 10 Energy 2 2014-01-01 2014-01-01 false Public hearings in proceedings for issuance of materials license with respect to a geologic repository. 51.109 Section 51.109 Energy NUCLEAR REGULATORY COMMISSION... Secretary of Energy; and (ii) The difference may significantly affect the quality of the human...

  14. 10 CFR 51.109 - Public hearings in proceedings for issuance of materials license with respect to a geologic...

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 10 Energy 2 2011-01-01 2011-01-01 false Public hearings in proceedings for issuance of materials license with respect to a geologic repository. 51.109 Section 51.109 Energy NUCLEAR REGULATORY COMMISSION... Secretary of Energy; and (ii) The difference may significantly affect the quality of the human...

  15. 10 CFR 51.109 - Public hearings in proceedings for issuance of materials license with respect to a geologic...

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 10 Energy 2 2012-01-01 2012-01-01 false Public hearings in proceedings for issuance of materials license with respect to a geologic repository. 51.109 Section 51.109 Energy NUCLEAR REGULATORY COMMISSION... Secretary of Energy; and (ii) The difference may significantly affect the quality of the human...

  16. 10 CFR 51.109 - Public hearings in proceedings for issuance of materials license with respect to a geologic...

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 10 Energy 2 2013-01-01 2013-01-01 false Public hearings in proceedings for issuance of materials license with respect to a geologic repository. 51.109 Section 51.109 Energy NUCLEAR REGULATORY COMMISSION... Secretary of Energy; and (ii) The difference may significantly affect the quality of the human...

  17. Present status and strategic plan for the stable isotope reference materials at the IAEA.

    NASA Astrophysics Data System (ADS)

    Assonov, Sergey; Groening, Manfred

    2016-04-01

    The presentation will give the overview of the stable isotope reference materials (SI-RMs) under distribution by the IAEA, its stable isotope laboratory and capacities related to material testing & production as well as future plans. Historically, most of the IAEA reference materials were produced and made available via collaborations with expert stable isotope laboratories worldwide. The IAEA plans include several directions as follows: • Maintaining the scale-defining SI-RMs at the highest level and introducing adequate replacements when needed; • Monitoring existing SI-RMs for any potential alteration(s) and of isotopic values assigned; • Identifying and then addressing the needs for new SI-RMs, with the priority to address the most critical applications (environmental and climate related applications, human health, food safety studies) and newly emerging analytical isotope techniques; • Performing all measurements aimed for characterisation of new SI-RMs and the corresponding uncertainty evaluation in accordance to the latest metrological concepts; • Promoting metrological approaches on traceability and uncertainty evaluation in every day practice of stable isotope measurements; • Expanding the IAEA capacities for SI-RMs by (i) planning a renewed laboratory at IAEA; (ii) enlarging collaboration with expert laboratories aimed to help IAEA in production and characterisation of new SI-RMs. These major directions will help to address the increasing demand for Stable Isotope Reference Materials.

  18. Development of candidate reference materials for the measurement of lead in bone

    PubMed Central

    Hetter, Katherine M.; Bellis, David J.; Geraghty, Ciaran; Todd, Andrew C.; Parsons, Patrick J.

    2010-01-01

    The production of modest quantities of candidate bone lead (Pb) reference materials is described, and an optimized production procedure is presented. The reference materials were developed to enable an assessment of the interlaboratory agreement of laboratories measuring Pb in bone; method validation; and for calibration of solid sampling techniques such as laser ablation ICP-MS. Long bones obtained from Pb-dosed and undosed animals were selected to produce four different pools of a candidate powdered bone reference material. The Pb concentrations of these pools reflect both environmental and occupational exposure levels in humans. The animal bones were harvested post mortem, cleaned, defatted, and broken into pieces using the brittle fracture technique at liquid nitrogen temperature. The bone pieces were then ground in a knife mill to produce fragments of 2-mm size. These were further ground in an ultra-centrifugal mill, resulting in finely powdered bone material that was homogenized and then sampled-scooped into vials. Testing for contamination and homogeneity was performed via instrumental methods of analysis. PMID:18421443

  19. Complete zircon and chromite digestion by sintering of granite, rhyolite, andesite and harzburgite rock reference materials for geochronological purposes

    NASA Astrophysics Data System (ADS)

    Bokhari, Syed Nadeem H.; Meisel, Thomas

    2014-05-01

    to be increased for an accurate content determination and complete release of analytes for geochronological studies. Larger test portion size reduces the heterogeneity issues in granites in particular [2]. No significant blanks issues were observed and interferences were controlled using QQQ MS mode of ICP-MS. References [1] Meisel, T., N. Schöner, et al. (2002). "Determination of Rare Earth Elements, Y, Th, Zr, Hf, Nb and Ta in Geological Reference Materials G-2, G-3, SCo-1 and WGB-1 by Sodium Peroxide Sintering and Inductively Coupled Plasma-Mass Spectrometry." Geostandards Newsletter 26(1): 53-61. [2] Bokhari SNH., Meisel T (2013) "The Determination of Homogeneity of Geological Reference Material" Mineralogical Magazine, 77(5): 731.

  20. Impact Craters on Earth: Lessons for Understanding Martian Geological Materials and Processes

    NASA Astrophysics Data System (ADS)

    Osinski, G. R.

    2015-12-01

    Impact cratering is one of the most ubiquitous geological processes in the Solar System and has had a significant influence on the geological evolution of Mars. Unlike the Moon and Mercury, the Martian impact cratering record is notably diverse, which is interpreted to reflect interactions during the impact process with target volatiles and/or the atmosphere. The Earth also possesses a volatile-rich crust and an atmosphere and so is one of the best analogues for understanding the effects of impact cratering on Mars. Furthermore, fieldwork at terrestrial craters and analysis of samples is critical to ground-truth observations made based on remote sensing data from Martian orbiters, landers, and rovers. In recent years, the effect of target lithology on various aspects of the impact cratering process has emerged as a major research topic. On Mars, volatiles have been invoked to be the primary factor influencing the morphology of ejecta deposits - e.g., the formation of single-, double- and multiple-layered ejecta deposits - and central uplifts - e.g., the formation of so-called "central pit" craters. Studies of craters on Earth have also shown that volatiles complicate the identification of impactites - i.e., rocks produced and/or affected by impact cratering. Identifying impactites on Earth is challenging, often requiring intensive and multi-technique laboratory analysis of hand specimens. As such, it is even more challenging to recognize such materials in remote datasets. Here, observations from the Haughton (d = 23 km; Canada), Ries (d = 24 km; Germany), Mistastin (d = 28 km; Canada), Tunnunik, (d = 28 km; Canada), and West Clearwater Lake (d = 36 km; Canada) impact structures are presented. First, it is shown that some impactites mimic intrusive, volcanic, volcanoclastic and in some cases sedimentary clastic rocks. Care should, therefore, be taken in the identification of seemingly unusual igneous rocks at rover landing sites as they may represent impact melt

  1. Determination of the 87Sr/86Sr isotope ratio in USGS silicate reference materials by multi-collector ICP-mass spectrometry

    NASA Astrophysics Data System (ADS)

    Balcaen, Lieve; Schrijver, Isabel De; Moens, Luc; Vanhaecke, Frank

    2005-04-01

    Multi-collector ICP-mass spectrometry (MC-ICP-MS) was used for 87Sr/86Sr isotope ratio determination in newly introduced silicate reference materials from the US Geological Survey (USGS): granite G-3, andesite AGV-2, and basalt BCR-2. Next to the SrCO3 isotopic standard NIST SRM 987, also analogous USGS reference materials from the previous generation, and for which reference 87Sr/86Sr data obtained by TIMS are available, were analysed for validation purposes. Sample preparation consisted of acid digestion and subsequent isolation of Sr by means of a dedicated and commercially available crown ether-based resin. The Sr fractions thus obtained were analysed via MC-ICP-MS whereby mass discrimination was corrected for internally, while the isobaric interference at a mass-to-charge ratio of 86 caused by Kr impurities in the Ar gas was mathematically corrected for by using the signal for a Kr isotope free from spectral overlap. Finally, also the effect of the small amount of Rb that may still be present in the Sr fraction was corrected for mathematically on the basis of the signal intensity for 85Rb. The MC-ICP-MS results for G-2, AGV-1 and BCR-1 showed an excellent agreement with the corresponding TIMS values (<0.003% bias in all cases), such that it can be assumed that also the 87Sr/86Sr isotope ratio results obtained for the new reference materials are reliable.

  2. Development of green onion and cabbage certified reference materials for quantification of organophosphorus and pyrethroid pesticides.

    PubMed

    Otake, Takamitsu; Yarita, Takashi; Aoyagi, Yoshie; Kuroda, Youko; Numata, Masahiko; Iwata, Hitoshi; Mizukoshi, Kazushi; Nakamura, Munetomo; Watai, Masatoshi; Mitsuda, Hitoshi; Fujikawa, Takashi; Ota, Hidekazu

    2011-08-24

    Green onion and cabbage certified reference materials for the analysis of pesticide residues were issued by the National Metrology Institute of Japan, part of the National Institute of Advanced Industrial Science and Technology. Green onion and cabbage samples were grown so as to contain several kinds of organophosphorus and pyrethroid pesticides, and those were collected from a field in the Kochi Prefecture in Japan. The certification was carried out by using multiple analytical methods to ensure the reliability of analytical results; the values of target pesticides (diazinon, fenitrothion, cypermethrin, etofenprox, and permethrin for green onion and chlorpyrifos, fenitrothion, and permethrin for cabbage) were obtained by isotope dilution mass spectrometry. Certified values of target pesticides were 0.96-13.9 and 2.41-6.9 mg/kg for green onion and cabbage, respectively. These are the first green onion and cabbage powder certified reference materials in which organophosphorus and pyrethroid pesticides are determined. PMID:21774469

  3. Reference Materials for Calibration of Analytical Biases in Quantification of DNA Methylation.

    PubMed

    Yu, Hannah; Hahn, Yoonsoo; Yang, Inchul

    2015-01-01

    Most contemporary methods for the quantification of DNA methylation employ bisulfite conversion and PCR amplification. However, many reports have indicated that bisulfite-mediated PCR methodologies can result in inaccurate measurements of DNA methylation owing to amplification biases. To calibrate analytical biases in quantification of gene methylation, especially those that arise during PCR, we utilized reference materials that represent exact bisulfite-converted sequences with 0% and 100% methylation status of specific genes. After determining relative quantities using qPCR, pairs of plasmids were gravimetrically mixed to generate working standards with predefined DNA methylation levels at 10% intervals in terms of mole fractions. The working standards were used as controls to optimize the experimental conditions and also as calibration standards in melting-based and sequencing-based analyses of DNA methylation. Use of the reference materials enabled precise characterization and proper calibration of various biases during PCR and subsequent methylation measurement processes, resulting in accurate measurements. PMID:26368560

  4. Prompt gamma activation analysis of boron in reference materials using diffracted polychromatic neutron beam

    NASA Astrophysics Data System (ADS)

    Byun, S. H.; Sun, G. M.; Choi, H. D.

    2004-01-01

    Boron concentrations were analyzed for standard reference materials by prompt gamma activation analysis (PGAA). The measurements were performed at the SNU-KAERI PGAA facility installed at Hanaro, the research reactor of Korea Atomic Energy Research Institute (KAERI). The facility uses a diffracted polychromatic beam with a neutron flux of 7.9 × 10 7 n/cm 2 s. Elemental sensitivity for boron was calibrated from the prompt gamma-ray spectra of boric acid samples containing 2-45 μg boron. The sensitivity of 2131 cps/mg-B was obtained from the linearity of the boron peak count rate versus the boron mass. The detection limit for boron was estimated to be 67 ng from an empty sample bag spectrum for a counting time of 10,000 s. The measured boron concentrations for standard reference materials showed good consistency with the certified or information values.

  5. Aflatoxin B1 in peanut meal reference materials: intercomparisons of methods.

    PubMed

    Van Egmond, H P; Wagstaffe, P J

    1989-01-01

    The Community Bureau of Reference (BCR) is preparing a series of animal feed reference materials to provide a basis for analytical quality assurance for aflatoxin B1 analysis, a problem of particular importance in view of Community legislation. Before reference values can be assigned to the reference materials the major errors in the underlying measurements must be identified and reduced. This paper presents the results of two intercomparison exercises involving some 20 European laboratories who applied a wide variety of analytical methods. It is shown that the major source of error and discrepancy is connected with incomplete extraction and/or losses during clean-up and that, provided correction for recovery/background interference is made, many methods can achieve acceptable accuracy. Sources of error and their control are discussed, and essential details of the methods used are presented. It is concluded that analytical QA is more important than the use of standardized methods when a high degree of accuracy and comparability are required. PMID:2498137

  6. Metrological approaches to organic chemical purity: primary reference materials for vitamin D metabolites.

    PubMed

    Nelson, Michael A; Bedner, Mary; Lang, Brian E; Toman, Blaza; Lippa, Katrice A

    2015-11-01

    Given the critical role of pure, organic compound primary reference standards used to characterize and certify chemical Certified Reference Materials (CRMs), it is essential that associated mass purity assessments be fit-for-purpose, represented by an appropriate uncertainty interval, and metrologically sound. The mass fraction purities (% g/g) of 25-hydroxyvitamin D (25(OH)D) reference standards used to produce and certify values for clinical vitamin D metabolite CRMs were investigated by multiple orthogonal quantitative measurement techniques. Quantitative (1)H-nuclear magnetic resonance spectroscopy (qNMR) was performed to establish traceability of these materials to the International System of Units (SI) and to directly assess the principal analyte species. The 25(OH)D standards contained volatile and water impurities, as well as structurally-related impurities that are difficult to observe by chromatographic methods or to distinguish from the principal 25(OH)D species by one-dimensional NMR. These impurities have the potential to introduce significant biases to purity investigations in which a limited number of measurands are quantified. Combining complementary information from multiple analytical methods, using both direct and indirect measurement techniques, enabled mitigation of these biases. Purities of 25(OH)D reference standards and associated uncertainties were determined using frequentist and Bayesian statistical models to combine data acquired via qNMR, liquid chromatography with UV absorbance and atmospheric pressure-chemical ionization mass spectrometric detection (LC-UV, LC-ACPI-MS), thermogravimetric analysis (TGA), and Karl Fischer (KF) titration.

  7. Transformation of paralytic shellfish poisoning toxins in Crassostrea gigas and Pecten maximus reference materials.

    PubMed

    Turner, Andrew D; Lewis, Adam M; Hatfield, Robert G; Galloway, Angus W; Higman, Wendy A

    2012-11-01

    Matrix reference materials are an important requirement for the assessment of method performance characteristics and for routine quality control. In the field of marine toxin testing where biological assays have been used and where modern analytical testing methods are now becoming available, this requirement has become an urgent one. Various approaches are utilised for preparation of such materials in the absence of available naturally occurring toxic shellfish samples. Toxin-free shellfish may be artificially fortified through the addition of cultured toxic phytoplankton or shellfish may be incurred through natural feeding on toxic algae in a laboratory environment. Both of these approaches may be potentially affected by issues relating to the degradation or transformation of toxin analytes, so studies were conducted to assess these effects within our laboratory. A range of PSP-toxic shellfish tissues were prepared using the two approaches, in both Pacific oyster (Crassostrea gigas) and king scallops (Pecten maximus). Additionally, sub-samples of incurred Pacific oyster tissue were further treated, through addition of artificial chemical stabilisers and gamma irradiation. Two separate month-long stability trials were conducted at +4 °C on each material. Results highlighted clear evidence for improved stability of materials following shellfish feeding experiments in comparison with the tissues which had been spiked with plankton. In addition, there were clear differences in stability of toxins between the two shellfish species studied. There was evidence for good stability of C1&2 toxins in both the incurred tissues and improved stability of some toxins in tissues which had been subjected to either gamma irradiation or treatment with chemical additives. The results therefore highlighted the benefits of conducting shellfish feeding if suitable stable reference materials are to be prepared containing a full range of PSP toxin analytes. The study also highlighted

  8. Novel application of high pressure processing for the production of shellfish toxin matrix reference materials.

    PubMed

    Turner, Andrew D; Powell, Andy L; Burrell, Stephen

    2014-11-01

    The production of homogeneous and stable matrix reference materials for marine biotoxins is important for the validation and implementation of instrumental methods of analysis. High pressure processing was investigated to ascertain potential advantages this technique may have in stabilising paralytic shellfish poisoning toxins in shellfish tissues compared to untreated materials. Oyster tissues were subjected to a range of different temperatures and pressures, with results showing a significant reduction in biological activity in comparison to control samples, without significantly altering toxin profiles. Tissue subjected to pressures >600 MPa at 50 °C was assessed for homogeneity and stability. The sample homogeneity was determined using a pre-column oxidation LC-FLD method and shown to be within accepted levels of within batch repeatability. Short and long-term stability studies were conducted over a range of temperatures, with analysis by pre and post column oxidation LC-FLD demonstrating improved stability of toxins compared to the untreated materials and with epimerisation of toxins also notably reduced in treated materials. This study confirmed the technique of high pressure processing to improve the stability of PSP toxins compared to untreated wet tissues and highlighted its applicability in reference material preparation where removal of biological activity is of importance.

  9. Novel application of high pressure processing for the production of shellfish toxin matrix reference materials.

    PubMed

    Turner, Andrew D; Powell, Andy L; Burrell, Stephen

    2014-11-01

    The production of homogeneous and stable matrix reference materials for marine biotoxins is important for the validation and implementation of instrumental methods of analysis. High pressure processing was investigated to ascertain potential advantages this technique may have in stabilising paralytic shellfish poisoning toxins in shellfish tissues compared to untreated materials. Oyster tissues were subjected to a range of different temperatures and pressures, with results showing a significant reduction in biological activity in comparison to control samples, without significantly altering toxin profiles. Tissue subjected to pressures >600 MPa at 50 °C was assessed for homogeneity and stability. The sample homogeneity was determined using a pre-column oxidation LC-FLD method and shown to be within accepted levels of within batch repeatability. Short and long-term stability studies were conducted over a range of temperatures, with analysis by pre and post column oxidation LC-FLD demonstrating improved stability of toxins compared to the untreated materials and with epimerisation of toxins also notably reduced in treated materials. This study confirmed the technique of high pressure processing to improve the stability of PSP toxins compared to untreated wet tissues and highlighted its applicability in reference material preparation where removal of biological activity is of importance. PMID:25086341

  10. The role of adequate reference materials in density measurements in hemodialysis

    NASA Astrophysics Data System (ADS)

    Furtado, A.; Moutinho, J.; Moura, S.; Oliveira, F.; Filipe, E.

    2015-02-01

    In hemodialysis, oscillation-type density meters are used to measure the density of the acid component of the dialysate solutions used in the treatment of kidney patients. An incorrect density determination of this solution used in hemodialysis treatments can cause several and adverse events to patients. Therefore, despite the Fresenius Medical Care (FME) tight control of the density meters calibration results, this study shows the benefits of mimic the matrix usually measured to produce suitable reference materials for the density meter calibrations.

  11. Development of benzene, toluene, ethylbenzene and xylenes certified gaseous reference materials

    NASA Astrophysics Data System (ADS)

    Brum, M. C.; Sobrinho, D. C. G.; Fagundes, F. A.; Oudwater, R. J.; Augusto, C. R.

    2016-07-01

    The work describes the production of certified gaseous reference materials of benzene, toluene, ethylbenzene and xylenes (BTEX) in nitrogen from the gravimetric production up to the long term stability tests followed by the certifying step. The uncertainty in the amount fractions of the compounds in these mixtures was approximately 4% (relative) for the range studied from 2 to 16 µmol/mol. Also the adsorption of the BTEX on the cylinder surface and the tubing were investigated as potential uncertainty source.

  12. Compositional analysis of biomass reference materials: Results from an interlaboratory study

    SciTech Connect

    Templeton, David W.; Wolfrum, Edward J.; Yen, James H.; Sharpless, Katherine E.

    2015-10-29

    Biomass compositional methods are used to compare different lignocellulosic feedstocks, to measure component balances around unit operations and to determine process yields and therefore the economic viability of biomass-to-biofuel processes. Four biomass reference materials (RMs NIST 8491–8494) were prepared and characterized, via an interlaboratory comparison exercise in the early 1990s to evaluate biomass summative compositional methods, analysts, and laboratories. Having common, uniform, and stable biomass reference materials gives the opportunity to assess compositional data compared to other analysts, to other labs, and to a known compositional value. The expiration date for the original characterization of these RMs was reached and an effort to assess their stability and recharacterize the reference values for the remaining material using more current methods of analysis was initiated. We sent samples of the four biomass RMs to 11 academic, industrial, and government laboratories, familiar with sulfuric acid compositional methods, for recharacterization of the component reference values. In this work, we have used an expanded suite of analytical methods that are more appropriate for herbaceous feedstocks, to recharacterize the RMs’ compositions. We report the median values and the expanded uncertainty values for the four RMs on a dry-mass, whole-biomass basis. The original characterization data has been recalculated using median statistics to facilitate comparisons with this data. We found improved total component closures for three out of the four RMs compared to the original characterization, and the total component closures were near 100 %, which suggests that most components were accurately measured and little double counting occurred. Here, the major components were not statistically different in the recharacterization which suggests that the biomass materials are stable during storage and that additional components, not seen in the original

  13. Compositional analysis of biomass reference materials: Results from an interlaboratory study

    DOE PAGESBeta

    Templeton, David W.; Wolfrum, Edward J.; Yen, James H.; Sharpless, Katherine E.

    2015-10-29

    Biomass compositional methods are used to compare different lignocellulosic feedstocks, to measure component balances around unit operations and to determine process yields and therefore the economic viability of biomass-to-biofuel processes. Four biomass reference materials (RMs NIST 8491–8494) were prepared and characterized, via an interlaboratory comparison exercise in the early 1990s to evaluate biomass summative compositional methods, analysts, and laboratories. Having common, uniform, and stable biomass reference materials gives the opportunity to assess compositional data compared to other analysts, to other labs, and to a known compositional value. The expiration date for the original characterization of these RMs was reached andmore » an effort to assess their stability and recharacterize the reference values for the remaining material using more current methods of analysis was initiated. We sent samples of the four biomass RMs to 11 academic, industrial, and government laboratories, familiar with sulfuric acid compositional methods, for recharacterization of the component reference values. In this work, we have used an expanded suite of analytical methods that are more appropriate for herbaceous feedstocks, to recharacterize the RMs’ compositions. We report the median values and the expanded uncertainty values for the four RMs on a dry-mass, whole-biomass basis. The original characterization data has been recalculated using median statistics to facilitate comparisons with this data. We found improved total component closures for three out of the four RMs compared to the original characterization, and the total component closures were near 100 %, which suggests that most components were accurately measured and little double counting occurred. Here, the major components were not statistically different in the recharacterization which suggests that the biomass materials are stable during storage and that additional components, not seen in the original

  14. Software Management Environment (SME) release 9.4 user reference material

    NASA Technical Reports Server (NTRS)

    Hendrick, R.; Kistler, D.; Manter, K.

    1992-01-01

    This document contains user reference material for the Software Management Environment (SME) prototype, developed for the Systems Development Branch (Code 552) of the Flight Dynamics Division (FDD) of Goddard Space Flight Center (GSFC). The SME provides an integrated set of management tools that can be used by software development managers in their day-to-day management and planning activities. This document provides an overview of the SME, a description of all functions, and detailed instructions concerning the software's installation and use.

  15. Compositional Analysis of Biomass Reference Materials: Results from an Interlaboratory Study

    PubMed Central

    Wolfrum, Edward J.; Yen, James H.; Sharpless, Katherine E.

    2016-01-01

    Biomass compositional methods are used to compare different lignocellulosic feedstocks, to measure component balances around unit operations and to determine process yields and therefore the economic viability of biomass-to-biofuel processes. Four biomass reference materials (RMs NIST 8491–8494) were prepared and characterized, via an interlaboratory comparison exercise in the early 1990s to evaluate biomass summative compositional methods, analysts, and laboratories. Having common, uniform, and stable biomass reference materials gives the opportunity to assess compositional data compared to other analysts, to other labs, and to a known compositional value. The expiration date for the original characterization of these RMs was reached and an effort to assess their stability and recharacterize the reference values for the remaining material using more current methods of analysis was initiated. We sent samples of the four biomass RMs to 11 academic, industrial, and government laboratories, familiar with sulfuric acid compositional methods, for recharacterization of the component reference values. In this work, we have used an expanded suite of analytical methods that are more appropriate for herbaceous feedstocks, to recharacterize the RMs’ compositions. We report the median values and the expanded uncertainty values for the four RMs on a dry-mass, whole-biomass basis. The original characterization data has been recalculated using median statistics to facilitate comparisons with this data. We found improved total component closures for three out of the four RMs compared to the original characterization, and the total component closures were near 100 %, which suggests that most components were accurately measured and little double counting occurred. The major components were not statistically different in the recharacterization which suggests that the biomass materials are stable during storage and that additional components, not seen in the original

  16. Adiabatic Calorimetry as Support to the Certification of High-Purity Liquid Reference Materials

    NASA Astrophysics Data System (ADS)

    Baldan, A.; Bosma, R.; Peruzzi, A.; van der Veen, A. M. H.; Shimizu, Y.

    2009-02-01

    The certification of high-purity liquid reference materials is supported by several analytical techniques (e.g., gas chromatography, liquid chromatography, Karl Fischer coulometry, inductively coupled plasma mass spectrometry, differential scanning calorimetry, adiabatic calorimetry). Most of them provide information on a limited set of specific impurities present in the sample (indirect methods). Adiabatic calorimetry [1] complementarily provides the overall molar fraction of impurities with sensitivity down to few μmol · mol-1 without giving any information about the nature of the impurities present in the sample (direct method). As the combination of adiabatic calorimetry with one (or more than one) indirect chemical techniques was regarded as an optimal methodology, NMi VSL developed an adiabatic calorimetry facility for the purity determination of high-purity liquid reference materials [2]. Within the framework of collaboration with NMIJ, a benzene-certified reference material (NMIJ CRM 4002) from NMIJ was analyzed by adiabatic calorimetry at NMi VSL. The results of this measurement are reported in this paper. Good agreement with the NMIJ-certified purity value (99.992 ± 0.003) cmol · mol-1 was found. The influence of different data analysis approaches (e.g., extrapolation functions, melting ranges) on the measurement results is reported. The uncertainty of the measured purity was estimated.

  17. Small-Angle Neutron Scattering study of the NIST mAb reference material

    NASA Astrophysics Data System (ADS)

    Castellanos, Maria Monica; Liu, Yun; Krueger, Susan; Curtis, Joseph

    Monoclonal antibodies (mAbs) are of great interest to the biopharmaceutical industry because they can be engineered to target specific antigens. Due to their importance, the biomanufacturing initiative at NIST is developing an IgG1 mAb reference material `NIST mAb', which can be used by industry, academia, and regulatory authorities. As part of this collaborative effort, we aim at characterizing the reference material using neutron scattering techniques. We have studied the small-angle scattering profile of the NIST mAb in a histidine buffer at 0 and 150 mM NaCl. Using Monte Carlo simulations, we generate an ensemble of structures and calculate their theoretical scattering profile, which can be directly compared with experimental data. Moreover, we analyze the structure factor to understand the effect of solution conditions on the protein-protein interactions. Finally, we have measured the solution scattering of the NIST mAb, while simultaneously performing freeze/thaw cycles, in order to investigate if the solution structure was affected upon freezing. The results from neutron scattering not only support the development of the reference material, but also provide insights on its stability and guide efforts for its development under different formulations.

  18. A CBNM 6Li spike isotopic reference material CBNM-IRM-615

    NASA Astrophysics Data System (ADS)

    Lamberty, A.; Verbruggen, A.; Hendrickx, F.; de Bièvre, P.

    1992-04-01

    A 6Li spike isotopic reference material CBNM-IRM-615 has been prepared in the form of Li2CO3 in HCl. The lithium concentration, (4.001 ± 0.028) × 10-3 mol Li kg-1, was determined by isotope dilution mass spectrometry against NBS SRM 924 Li2CO3. CBNM-IRM-615 is certified for its isotopic composition: 95.610 ± 0.025 amount % 6Li; 4.390 ± 0.025 amount % 7Li; and for its 6Li concentration: 3.825 ± 0.027 × 10-3 mol 6Li kg-1 of solution. Uncertainties are 2s or the equivalent estimate thereof. The isotopic reference material is available in quartz ampoules containing approximately 5 g of solution. Using this spike isotopic reference material. 7Li or total Li concentrations in unknown samples can be determined by isotope dilution mass spectrometry via a measurement of the molar isotope dilution ratio RB = 6Li/7Li in the blend.

  19. Material Units, Structures/Landforms, and Stratigraphy for the Global Geologic Map of Ganymede (1:15M)

    NASA Technical Reports Server (NTRS)

    Patterson, G. Wesley; Head, James W.; Collins, Geoffrey C.; Pappalardo, Robert T.; Prockter, Louis M.; Lucchitta, Baerbel K.

    2008-01-01

    In the coming year a global geological map of Ganymede will be completed that represents the most recent understanding of the satellite on the basis of Galileo mission results. This contribution builds on important previous accomplishments in the study of Ganymede utilizing Voyager data and incorporates the many new discoveries that were brought about by examination of Galileo data. Material units have been defined, structural landforms have been identified, and an approximate stratigraphy has been determined utilizing a global mosaic of the surface with a nominal resolution of 1 km/pixel assembled by the USGS. This mosaic incorporates the best available Voyager and Galileo regional coverage and high resolution imagery (100-200 m/pixel) of characteristic features and terrain types obtained by the Galileo spacecraft. This map has given us a more complete understanding of: 1) the major geological processes operating on Ganymede, 2) the characteristics of the geological units making up its surface, 3) the stratigraphic relationships of geological units and structures, and 4) the geological history inferred from these relationships. A summary of these efforts is provided here.

  20. Geology of the Williston basin, North Dakota, Montana, and South Dakota, with reference to subsurface disposal of radioactive wastes

    USGS Publications Warehouse

    Sandberg, C.A.

    1962-01-01

    The southern Williston basin, which underlies about 110,000 square miles #n North Dakota, South Dakota, and eastern Montana, is part of a large structural and sedimentary basin. Its surface is a flat to gently rolling plain, standing about 1,500 to 3,500 feet above sea level and locally studded by a few high buttes. The sedimentary sequence that fills the basin has a maximum thickness of about 16,700 feet and rests on Precambrian metamorphic rocks at depths of 500 to 13,900 feet below sea level. It contains rocks of every geologic system, from Cambrian to Quaternary. Rocks of Middle Cambrian through Middle Ordovician age are largely shale and sandstone, as much as 1,200 feet thick; rocks of Late Ordovician through Pennsylvanian age are largely limestone and dolomite, as much as 7,500 feet thick; and rocks of Permian through Tertiary age are predominantly shale and siltstone, as much as 8,000 feet thick. Pleistocene glacial drift mantles the northern and eastern parts of the area. Rocks of the Williston basin are gently folded and regional dips are 1? or less from the margins to the basin center. Dips on the flanks of the major anticlinal folds, the Nesson and cedar Creek anticlines and the Poplar and Bowdoin domes, generally are about 1? to 3? except on the steep west limb of the Cedar Creek anticline. The basin was shaped by Laramide orogeny during latest Cretaceous and early Tertiary time. Most of the present structural features, however, were initiated during the Precambrian and reactivated by several subsequent orogenies, of which the latest was the Laramide. The most important mineral resource of the area is oil, which is produced predominantly from the Paleozoic carbonate sequence and largely on three of the major anticlinal folds, and lignite, which is present near the surface in Paleocene rocks. The subsurface disposal of radioactive wastes at some places in the Williston basin appears to be geographically and geologically feasible. Many sites, at which

  1. Characterization of Pu concentration and its isotopic composition in a reference fallout material.

    PubMed

    Zhang, Yongsan; Zheng, Jian; Yamada, Masatoshi; Wu, Fengchang; Igarashi, Yasuhito; Hirose, Katsumi

    2010-02-01

    Because there is no reference material for fallout plutonium isotope monitoring, preparation of such a material is necessary for quality control of fallout radionuclides analysis for atmospheric environmental studies. In this work, we report the characterization of Pu activity and its isotopic composition in a reference fallout material prepared by the Meteorological Research Institute (MRI), Japan. This material was prepared from samples collected at 14 stations throughout Japan in 1963-1979, with reference values of (137)Cs, (90)Sr and (239)(+)(240)Pu activities. We analyzed the activities of (239)(+)(240)Pu and (241)Pu, and the atom ratios of (240)Pu/(239)Pu and (241)Pu/(239)Pu using an isotope dilution sector-field inductively coupled plasma mass spectrometry (SF-ICP-MS). The (239)(+)(240)Pu activities in this fallout material using acid leaching and total digestion were 6.56+/-0.20 mBq/g and 6.79+/-0.16 mBq/g, respectively. Atom ratios of (240)Pu/(239)Pu were 0.1915+/-0.0030 and 0.1922+/-0.0044, respectively. Both (240)Pu/(239)Pu and (241)Pu/(239)Pu atom ratios were slightly higher than those of global fallout, which could be attributed to the deposition of fallout radionuclides resulting from the Chinese nuclear weapons tests conducted in the 1970s. The dominant host phases of (239)(+)(240)Pu were found to be organic matter-sulfides (70%) with a relative high (240)Pu/(239)Pu atom ratio, and Fe-Mn oxides (19%) using a sequential extraction method.

  2. Exploration of optical fibres as a carrier for new benzene and toluene matrix-free reference materials.

    PubMed

    Słomińska, Marta; Marć, Mariusz; Szczygelska-Tao, Jolanta; Konieczka, Piotr; Namieśnik, Jacek

    2015-07-01

    To meet high expectations concerning precision and accuracy of reference materials, preparation of matrix-free reference materials using thermal decomposition-gas chromatography-mass spectrometry (TD-GC-MS) was proposed in this study. In the paper, the results obtained in preparation of the new reference materials for benzene and toluene are presented, based on the thermal decomposition technique of compounds chemically bound to the surface of optical fibre segments. The results obtained at various stages of the research procedure (homogeneity, stability) confirmed the possibility of using prepared laboratory samples of materials as reference materials for benzene and toluene. For the prepared batch of materials, reference values 1.26 ± 0.91 (ng/fibre) for benzene and 11.3 ± 7.4 (ng/fibre) for toluene were determined.

  3. Development of a certified reference material for genetically modified potato with altered starch composition.

    PubMed

    Broothaerts, Wim; Corbisier, Philippe; Emons, Hendrik; Emteborg, Håkan; Linsinger, Thomas P J; Trapmann, Stefanie

    2007-06-13

    The presence of genetically modified organisms (GMOs) in food and feed products is subject to regulation in the European Union (EU) and elsewhere. As part of the EU authorization procedure for GMOs intended for food and feed use, reference materials must be produced for the quality control of measurements to quantify the GMOs. Certified reference materials (CRMs) are available for a range of herbicide- and insect-resistant genetically modified crops such as corn, soybean, and cotton. Here the development of the first CRM for a GMO that differs from its non-GMO counterpart in a major compositional constituent, that is, starch, is described. It is shown that the modification of the starch composition of potato (Solanum tuberosum L.) tubers, together with other characteristics of the delivered materials, have important consequences for the certification strategy. Moreover, the processing and characterization of the EH92-527-1 potato material required both new and modified procedures, different from those used routinely for CRMs produced from genetically modified seeds. PMID:17508757

  4. Validation of reference materials for uranium radiochronometry in the frame of nuclear forensic investigations.

    PubMed

    Varga, Z; Mayer, K; Bonamici, C E; Hubert, A; Hutcheon, I; Kinman, W; Kristo, M; Pointurier, F; Spencer, K; Stanley, F; Steiner, R; Tandon, L; Williams, R

    2015-08-01

    The results of a joint effort by expert nuclear forensic laboratories in the area of age dating of uranium, i.e. the elapsed time since the last chemical purification of the material are presented and discussed. Completely separated uranium materials of known production date were distributed among the laboratories, and the samples were dated according to routine laboratory procedures by the measurement of the (230)Th/(234)U ratio. The measurement results were in good agreement with the known production date showing that the concept for preparing uranium age dating reference material based on complete separation is valid. Detailed knowledge of the laboratory procedures used for uranium age dating allows the identification of possible improvements in the current protocols and the development of improved practice in the future. The availability of age dating reference materials as well as the evolvement of the age dating best-practice protocol will increase the relevance and applicability of age dating as part of the tool-kit available for nuclear forensic investigations.

  5. Developing a reference material for diffusion-controlled formaldehyde emissions testing.

    PubMed

    Liu, Zhe; Liu, Xiaoyu; Zhao, Xiaomin; Cox, Steven S; Little, John C

    2013-11-19

    Formaldehyde, a known human carcinogen and mucous membrane irritant, is emitted from a variety of building materials and indoor furnishings. The drive to improve building energy efficiency by decreasing ventilation rates increases the need to better understand emissions from indoor products and to identify and develop lower emitting materials. To help meet this need, formaldehyde emissions from indoor materials are typically measured using environmental chambers. However, chamber testing results are frequently inconsistent and provide little insight into the mechanisms governing emissions. This research addresses these problems by (1) developing a reference formaldehyde emissions source that can be used to validate chamber testing methods for characterization of dynamic sources of formaldehyde emissions and (2) demonstrating that emissions from finite formaldehyde sources can be predicted using a fundamental mass-transfer model. Formaldehyde mass-transfer mechanisms are elucidated, providing practical approaches for developing diffusion-controlled reference materials that mimic actual sources. The fundamental understanding of emissions mechanisms can be used to improve emissions testing and guide future risk reduction actions.

  6. Developing a reference material for diffusion-controlled formaldehyde emissions testing.

    PubMed

    Liu, Zhe; Liu, Xiaoyu; Zhao, Xiaomin; Cox, Steven S; Little, John C

    2013-11-19

    Formaldehyde, a known human carcinogen and mucous membrane irritant, is emitted from a variety of building materials and indoor furnishings. The drive to improve building energy efficiency by decreasing ventilation rates increases the need to better understand emissions from indoor products and to identify and develop lower emitting materials. To help meet this need, formaldehyde emissions from indoor materials are typically measured using environmental chambers. However, chamber testing results are frequently inconsistent and provide little insight into the mechanisms governing emissions. This research addresses these problems by (1) developing a reference formaldehyde emissions source that can be used to validate chamber testing methods for characterization of dynamic sources of formaldehyde emissions and (2) demonstrating that emissions from finite formaldehyde sources can be predicted using a fundamental mass-transfer model. Formaldehyde mass-transfer mechanisms are elucidated, providing practical approaches for developing diffusion-controlled reference materials that mimic actual sources. The fundamental understanding of emissions mechanisms can be used to improve emissions testing and guide future risk reduction actions. PMID:24102115

  7. Determination of perfluorinated alkyl acid concentrations in biological standard reference materials.

    PubMed

    Reiner, Jessica L; O'Connell, Steven G; Butt, Craig M; Mabury, Scott A; Small, Jeff M; De Silva, Amila O; Muir, Derek C G; Delinsky, Amy D; Strynar, Mark J; Lindstrom, Andrew B; Reagen, William K; Malinsky, Michelle; Schäfer, Sandra; Kwadijk, Christiaan J A F; Schantz, Michele M; Keller, Jennifer M

    2012-11-01

    Standard reference materials (SRMs) are homogeneous, well-characterized materials used to validate measurements and improve the quality of analytical data. The National Institute of Standards and Technology (NIST) has a wide range of SRMs that have mass fraction values assigned for legacy pollutants. These SRMs can also serve as test materials for method development, method validation, and measurement for contaminants of emerging concern. Because inter-laboratory comparison studies have revealed substantial variability of measurements of perfluoroalkyl acids (PFAAs), future analytical measurements will benefit from determination of consensus values for PFAAs in SRMs to provide a means to demonstrate method-specific performance. To that end, NIST, in collaboration with other groups, has been measuring concentrations of PFAAs in a variety of SRMs. Here we report levels of PFAAs and perfluorooctane sulfonamide (PFOSA) determined in four biological SRMs: fish tissue (SRM 1946 Lake Superior Fish Tissue, SRM 1947 Lake Michigan Fish Tissue), bovine liver (SRM 1577c), and mussel tissue (SRM 2974a). We also report concentrations for three in-house quality-control materials: beluga whale liver, pygmy sperm whale liver, and white-sided dolphin liver. Measurements in SRMs show an array of PFAAs, with perfluorooctane sulfonate (PFOS) being the most frequently detected. Reference and information values are reported for PFAAs measured in these biological SRMs. PMID:22476786

  8. 230Th-234U Model-Ages of Some Uranium Standard Reference Materials

    SciTech Connect

    Williams, R W; Gaffney, A M; Kristo, M J; Hutcheon, I D

    2009-05-28

    The 'age' of a sample of uranium is an important aspect of a nuclear forensic investigation and of the attribution of the material to its source. To the extent that the sample obeys the standard rules of radiochronometry, then the production ages of even very recent material can be determined using the {sup 230}Th-{sup 234}U chronometer. These standard rules may be summarized as (a) the daughter/parent ratio at time=zero must be known, and (b) there has been no daughter/parent fractionation since production. For most samples of uranium, the 'ages' determined using this chronometer are semantically 'model-ages' because (a) some assumption of the initial {sup 230}Th content in the sample is required and (b) closed-system behavior is assumed. The uranium standard reference materials originally prepared and distributed by the former US National Bureau of Standards and now distributed by New Brunswick Laboratory as certified reference materials (NBS SRM = NBL CRM) are good candidates for samples where both rules are met. The U isotopic standards have known purification and production dates, and closed-system behavior in the solid form (U{sub 3}O{sub 8}) may be assumed with confidence. We present here {sup 230}Th-{sup 234}U model-ages for several of these standards, determined by isotope dilution mass spectrometry using a multicollector ICP-MS, and compare these ages with their known production history.

  9. Development of a certified reference material for genetically modified potato with altered starch composition.

    PubMed

    Broothaerts, Wim; Corbisier, Philippe; Emons, Hendrik; Emteborg, Håkan; Linsinger, Thomas P J; Trapmann, Stefanie

    2007-06-13

    The presence of genetically modified organisms (GMOs) in food and feed products is subject to regulation in the European Union (EU) and elsewhere. As part of the EU authorization procedure for GMOs intended for food and feed use, reference materials must be produced for the quality control of measurements to quantify the GMOs. Certified reference materials (CRMs) are available for a range of herbicide- and insect-resistant genetically modified crops such as corn, soybean, and cotton. Here the development of the first CRM for a GMO that differs from its non-GMO counterpart in a major compositional constituent, that is, starch, is described. It is shown that the modification of the starch composition of potato (Solanum tuberosum L.) tubers, together with other characteristics of the delivered materials, have important consequences for the certification strategy. Moreover, the processing and characterization of the EH92-527-1 potato material required both new and modified procedures, different from those used routinely for CRMs produced from genetically modified seeds.

  10. Stand-off laser-induced breakdown spectroscopy of aluminum and geochemical reference materials at pressure below 1 torr

    NASA Astrophysics Data System (ADS)

    Lee, Kang-Jae; Choi, Soo-Jin; Yoh, Jack J.

    2014-11-01

    Laser-induced breakdown spectroscopy (LIBS) is an atomic emission spectroscopy that utilizes a highly irradiated pulse laser focused on the target surface to produce plasma. We obtain spectroscopic information from the microplasma and determine the chemical composition of the sample based on its elemental and molecular emission peaks. We develop a stand-off LIBS system to analyze the effect of the remote sensing of aluminum and various geochemical reference materials at pressures below 1 torr. Using a commercial 4 inch refracting telescope, our stand-off LIBS system is configured at a distance of 7.2 m from the four United States Geological Survey (USGS) geochemical samples that include granodiorite, quartz latite, shale-cody, and diabase, which are selected for planetary exploration. Prepared samples were mixed with a paraffin binder containing only hydrogen and carbon, and were pelletized for experimental convenience. The aluminum plate sample is considered as a reference prior to using the geochemical samples in order to understand the influence of a low pressure condition on the resulting LIBS signal. A Q-switched Nd:YAG laser operating at 1064 nm and pulsed at 10 Hz with 21.7 to 48.5 mJ/pulse was used to obtain signals, which showed that the geochemical samples were successfully detected by the present stand-off detection scheme. A low pressure condition generally results in a decrease of the signal intensity, while the signal to noise ratio can vary according to the samples and elements of various types. We successfully identified the signals at below 1 torr with stand-off detection by a tightly focused light detection and by using a relatively larger aperture telescope. The stand-off LIBS detection at low pressure is promising for potential detection of the minor elements at pressures below 1 torr.

  11. Hf Isotope Geochemistry of USGS Reference Materials and Various Labware: Insight into Potential Contaminant Sources

    NASA Astrophysics Data System (ADS)

    Weis, D.; Nobre Silva, I.; Kieffer, B.; Barling, J.; Pretorius, W.; Maerschalk, C.

    2005-12-01

    We have undertaken a high-precision geochemical and isotopic study of USGS reference materials by HR-ICP-MS, TIMS and MC-ICP-MS, including basalt (BCR-1,2; BHVO-1,2), andesite (AGV-1,2), rhyolite (RGM-1), syenite (STM-1,2), granodiorite (GSP-2), and granite (G-2,3). Only a few 176Hf/177Hf results are published on these materials and with the increased use of MC-ICP-MS it is critical to build a solid reference database. Standard hotplate dissolution was used, except for granitoid compositions where it involved a high-pressure bomb procedure. The reproducibility of 176Hf/177Hf is better than 100 ppm for granitoid compositions (G-2: 0.282523±8; G-3: 0.282505±20; GSP-2: 0.282059±27) and better than 65 ppm for basaltic/andesitic compositions in glassware and better than 30 ppm in teflon (BCR-2: 0.282872±9; BHVO-2: 0.283103±6). Overall, our results agree with the rare published data (BCR-1&2, BHVO-1 and RGM-1). Slight differences appear depending on the chemical procedure used to separate Hf and the type of labware used. There are systematic shifts in 176Hf/177Hf for basaltic compositions towards lower values (by 100-150 ppm) when non-teflon material is used. As a result, we then carried out a systematic trace element and isotopic study of various labware, including borosilicate glass and quartz columns and frits. Maximum concentrations (in ppm) of these materials (in the order listed above) are: Hf=16-0.3-22, Nd=0.8-0.1-23, Sr=8-0.08-16, Pb=1.4-0.5-14. The frit material appears the most variable in elemental concentration and isotopic composition, which might reflect various accumulations resulting from column chemistry. 176Hf/177Hf is 0.282198±4 in borosilicate glass and even lower in some of the frit material (<0.28195). Only a small amount of such unradiogenic material can account for the shifts observed in basaltic rocks. Our systematic study shows that careful analyses of rock reference materials with different compositional matrices are necessary, in

  12. Reference Material Kydex(registered trademark)-100 Test Data Message for Flammability Testing

    NASA Technical Reports Server (NTRS)

    Engel, Carl D.; Richardson, Erin; Davis, Eddie

    2003-01-01

    The Marshall Space Flight Center (MSFC) Materials and Processes Technical Information System (MAPTIS) database contains, as an engineering resource, a large amount of material test data carefully obtained and recorded over a number of years. Flammability test data obtained using Test 1 of NASA-STD-6001 is a significant component of this database. NASA-STD-6001 recommends that Kydex 100 be used as a reference material for testing certification and for comparison between test facilities in the round-robin certification testing that occurs every 2 years. As a result of these regular activities, a large volume of test data is recorded within the MAPTIS database. The activity described in this technical report was undertaken to mine the database, recover flammability (Test 1) Kydex 100 data, and review the lessons learned from analysis of these data.

  13. On the status of IAEA delta-13C stable isotope reference materials.

    NASA Astrophysics Data System (ADS)

    Assonov, Sergey; Groening, Manfred; Fajgelj, Ales

    2016-04-01

    For practical reasons all isotope measurements are performed on relative scales realized through the use of international, scale-defining primary standards. In fact these standards were materials (artefacts, similar to prototypes of meter and kg) selected based on their properties. The VPDB delta-13C scale is realised via two highest-level reference materials NBS19 and LSVEC, the first defining the scale and the second aimed to normalise lab-to-lab calibrations. These two reference materials (RMs) have been maintained and distributed by IAEA and NIST. The priority task is to maintain these primary RMs at the required uncertainty level, thus ensuring the long-term scale consistency. The second task is to introduce replacements when needed (currently for exhausted NBS19, work in progress). The next is to produce a family of lower level RMs (secondary, tertiary) addressing needs of various applications (with different delta values, in different physical-chemical forms) and their needs for the uncertainty; these RMs should be traceable to the highest level RMs. Presently three is a need for a range of RMs addressing existing and newly emerging analytical techniques (e.g. optical isotopic analysers) in form of calibrated CO2 gases with different delta-13C values. All that implies creating a family of delta-13C stable isotope reference materials. Presently IAEA works on replacement for NBS19 and planning new RMs. Besides, we found that LSVEC (introduced as second anchor for the VPDB scale in 2006) demonstrate a considerable scatter of its delta-13C value which implies a potential bias of the property value and increased value uncertainty which may conflict with uncertainty requirements for atmospheric monitoring. That is not compatible with the status of LSVEC, and therefore it should be replaced as soon as possible. The presentation will give an overview of the current status, the strategic plan of developments and the near future steps.

  14. Development of botanical and fish oil standard reference materials for fatty acids.

    PubMed

    Schantz, Michele M; Sander, Lane C; Sharpless, Katherine E; Wise, Stephen A; Yen, James H; NguyenPho, Agnes; Betz, Joseph M

    2013-05-01

    As part of a collaboration with the National Institutes of Health's Office of Dietary Supplements and the Food and Drug Administration's Center for Drug Evaluation and Research, the National Institute of Standards and Technology has developed Standard Reference Material (SRM) 3274 Botanical Oils Containing Omega-3 and Omega-6 Fatty Acids and SRM 3275 Omega-3 and Omega-6 Fatty Acids in Fish Oil. SRM 3274 consists of one ampoule of each of four seed oils (3274-1 Borage (Borago officinalis), 3274-2 Evening Primrose (Oenothera biennis), 3274-3 Flax (Linium usitatissimum), and 3274-4 Perilla (Perilla frutescens)), and SRM 3275 consists of two ampoules of each of three fish oils (3275-1 a concentrate high in docosahexaenoic acid, 3275-2 an anchovy oil high in docosahexaenoic acid and eicosapentaenoic acid, and 3275-3 a concentrate containing 60% long-chain omega-3 fatty acids). Each oil has certified and reference mass fraction values for up to 20 fatty acids. The fatty acid mass fraction values are based on results from analyses using gas chromatography with flame ionization detection (GC-FID) and mass spectrometry (GC/MS). These SRMs will complement other reference materials currently available with mass fractions for similar analytes and are part of a series of SRMs being developed for dietary supplements. PMID:23371533

  15. Development of botanical and fish oil standard reference materials for fatty acids.

    PubMed

    Schantz, Michele M; Sander, Lane C; Sharpless, Katherine E; Wise, Stephen A; Yen, James H; NguyenPho, Agnes; Betz, Joseph M

    2013-05-01

    As part of a collaboration with the National Institutes of Health's Office of Dietary Supplements and the Food and Drug Administration's Center for Drug Evaluation and Research, the National Institute of Standards and Technology has developed Standard Reference Material (SRM) 3274 Botanical Oils Containing Omega-3 and Omega-6 Fatty Acids and SRM 3275 Omega-3 and Omega-6 Fatty Acids in Fish Oil. SRM 3274 consists of one ampoule of each of four seed oils (3274-1 Borage (Borago officinalis), 3274-2 Evening Primrose (Oenothera biennis), 3274-3 Flax (Linium usitatissimum), and 3274-4 Perilla (Perilla frutescens)), and SRM 3275 consists of two ampoules of each of three fish oils (3275-1 a concentrate high in docosahexaenoic acid, 3275-2 an anchovy oil high in docosahexaenoic acid and eicosapentaenoic acid, and 3275-3 a concentrate containing 60% long-chain omega-3 fatty acids). Each oil has certified and reference mass fraction values for up to 20 fatty acids. The fatty acid mass fraction values are based on results from analyses using gas chromatography with flame ionization detection (GC-FID) and mass spectrometry (GC/MS). These SRMs will complement other reference materials currently available with mass fractions for similar analytes and are part of a series of SRMs being developed for dietary supplements.

  16. Isotopic composition ( 238U/ 235U) of some commonly used uranium reference materials

    NASA Astrophysics Data System (ADS)

    Condon, Daniel J.; McLean, Noah; Noble, Stephen R.; Bowring, Samuel A.

    2010-12-01

    We have determined 238U/ 235U ratios for a suite of commonly used natural (CRM 112a, SRM 950a, and HU-1) and synthetic (IRMM 184 and CRM U500) uranium reference materials by thermal ionisation mass-spectrometry (TIMS) using the IRMM 3636 233U- 236U double spike to accurately correct for mass fractionation. Total uncertainty on the 238U/ 235U determinations is estimated to be <0.02% (2σ). These natural 238U/ 235U values are different from the widely used 'consensus' value (137.88), with each standard having lower 238U/ 235U values by up to 0.08%. The 238U/ 235U ratio determined for CRM U500 and IRMM 184 are within error of their certified values; however, the total uncertainty for CRM U500 is substantially reduced (from 0.1% to 0.02%). These reference materials are commonly used to assess mass-spectrometer performance and accuracy, calibrate isotope tracers employed in U, U-Th and U-Pb isotopic studies, and as a reference for terrestrial and meteoritic 238U/ 235U variations. These new 238U/ 235U values will thus provide greater accuracy and reduced uncertainty for a wide variety of isotopic determinations.

  17. Statistical Analysis of a Round-Robin Measurement Survey of Two Candidate Materials for a Seebeck Coefficient Standard Reference Material

    PubMed Central

    Lu, Z. Q. J.; Lowhorn, N. D.; Wong-Ng, W.; Zhang, W.; Thomas, E. L.; Otani, M.; Green, M. L.; Tran, T. N.; Caylor, C.; Dilley, N. R.; Downey, A.; Edwards, B.; Elsner, N.; Ghamaty, S.; Hogan, T.; Jie, Q.; Li, Q.; Martin, J.; Nolas, G.; Obara, H.; Sharp, J.; Venkatasubramanian, R.; Willigan, R.; Yang, J.; Tritt, T.

    2009-01-01

    In an effort to develop a Standard Reference Material (SRM™) for Seebeck coefficient, we have conducted a round-robin measurement survey of two candidate materials—undoped Bi2Te3 and Constantan (55 % Cu and 45 % Ni alloy). Measurements were performed in two rounds by twelve laboratories involved in active thermoelectric research using a number of different commercial and custom-built measurement systems and techniques. In this paper we report the detailed statistical analyses on the interlaboratory measurement results and the statistical methodology for analysis of irregularly sampled measurement curves in the interlaboratory study setting. Based on these results, we have selected Bi2Te3 as the prototype standard material. Once available, this SRM will be useful for future interlaboratory data comparison and instrument calibrations. PMID:27504212

  18. History of reference materials for food and nutrition metrology: As represented in the series of BERM Symposia

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Establishment of a metrology-based measurement system requires the solid foundation of traceability of measurements to available, appropriate certified reference materials (CRM). In the early 1970s the first “biological” Reference Material (RM) of Bowens Kale, Orchard Leaves, and Bovine Liver from ...

  19. Geology of the Powder River Basin, Wyoming and Montana, with reference to subsurface disposal of radioactive wastes

    USGS Publications Warehouse

    Beikman, Helen M.

    1962-01-01

    The Powder River Basin is a structural and topographic basin occupying an area of about 20,000 square miles in northeastern Wyoming arid southeastern Montana. The Basin is about 230 miles long in a northwest-southeast direction and is about 100 miles wide. It is bounded on three sides by mountains in which rocks of Precambrian age are exposed. The Basin is asymmetrical with a steep west limb adjacent to the Bighorn Mountains and a gentle east limb adjacent to the Black Hills. Sedimentary rocks within the Basin have a maximum thickness of about 18,000 feet and rocks of every geologic period are represented. Paleozoic rocks are about 2,500 feet thick and consist of marine bonate rocks and sandstone; Mesozoic rocks are about 9,500 feet thick and consist of both marine and nonmarine siltstone and sandstone; and Cenozoic rocks are from 4,000 to 6,000 feet thick and consist of coal-bearing sandstone and shale. Radioactive waste could be stored in the pore space of permeable sandstone or in shale where space could be developed. Many such rock units that could be used for storing radioactive wastes are present within the Powder River Basin. Permeable sandstone beds that may be possible reservoirs for storage of radioactive waste are present throughout the Powder River Basin. These include sandstone beds in the Flathead Sandstone and equivalent strata in the Deadwood Formation, the Tensleep Sandstone and equivalent strata in the Minnelusa Formation and the Sundance Formation in rocks of pre-Cretaceous age. However, most of the possible sandstone reservoirs are in rocks of Cretaceous age and include sandstone beds in the Fall River, Lakota, Newcastle, Frontier, Cody, and Mesaverde Formations. Problems of containment of waste such as clogging of pore space and chemical incompatibility would have to be solved before a particular sandstone unit could be selected for waste disposal. Several thick sequences of impermeable shale such as those in the Skull Creek, Mowry, Frontier

  20. Reference waste forms and packing material for the Nevada Nuclear Waste Storage Investigations Project

    SciTech Connect

    Oversby, V.M.

    1984-03-30

    The Lawrence Livermore National Laboratory (LLNL), Livermore, Calif., has been given the task of designing and verifying the performance of waste packages for the Nevada Nuclear Waste Storage Investigations (NNWSI) Project. NNWSI is studying the suitability of the tuffaceous rocks at Yucca Mountain, Nevada Test Site, for the potential construction of a high-level nuclear waste repository. This report gives a summary description of the three waste forms for which LLNL is designing waste packages: spent fuel, either as intact assemblies or as consolidated fuel pins, reprocessed commercial high-level waste in the form of borosilicate glass, and reprocessed defense high-level waste from the Defense Waste Processing Facility in Aiken, S.C. Reference packing material for use with the alternative waste package design for spent fuel is also described. 14 references, 8 figures, 20 tables.

  1. Results of a Saxitoxin Proficiency Test Including Characterization of Reference Material and Stability Studies

    PubMed Central

    Harju, Kirsi; Rapinoja, Marja-Leena; Avondet, Marc-André; Arnold, Werner; Schär, Martin; Luginbühl, Werner; Kremp, Anke; Suikkanen, Sanna; Kankaanpää, Harri; Burrell, Stephen; Söderström, Martin; Vanninen, Paula

    2015-01-01

    A saxitoxin (STX) proficiency test (PT) was organized as part of the Establishment of Quality Assurance for the Detection of Biological Toxins of Potential Bioterrorism Risk (EQuATox) project. The aim of this PT was to provide an evaluation of existing methods and the European laboratories’ capabilities for the analysis of STX and some of its analogues in real samples. Homogenized mussel material and algal cell materials containing paralytic shellfish poisoning (PSP) toxins were produced as reference sample matrices. The reference material was characterized using various analytical methods. Acidified algal extract samples at two concentration levels were prepared from a bulk culture of PSP toxins producing dinoflagellate Alexandrium ostenfeldii. The homogeneity and stability of the prepared PT samples were studied and found to be fit-for-purpose. Thereafter, eight STX PT samples were sent to ten participating laboratories from eight countries. The PT offered the participating laboratories the possibility to assess their performance regarding the qualitative and quantitative detection of PSP toxins. Various techniques such as official Association of Official Analytical Chemists (AOAC) methods, immunoassays, and liquid chromatography-mass spectrometry were used for sample analyses. PMID:26602927

  2. Development and certification of a reference material for Fusarium mycotoxins in wheat flour.

    PubMed

    Köppen, Robert; Bremser, Wolfram; Rasenko, Tatjana; Koch, Matthias

    2013-05-01

    Deoxynivalenol (DON), nivalenol (NIV) and zearalenone (ZEN) are toxic secondary metabolites produced by several species of Fusarium fungi. These mycotoxins are often found together in a large variety of cereal-based foods, which are regulated by maximum content levels of DON and ZEN. To date, suitable certified reference materials (CRM) intended for quality control purposes are lacking for these Fusarium mycotoxins. In order to overcome this lack, the first CRM for the determination of DON, NIV and ZEN in naturally contaminated wheat flour (ERM®-BC600) was developed in the framework of a European Reference Materials (ERM®) project. This article describes and discusses the whole process of ERM®-BC600 development, including material preparation, homogeneity and stability studies, and an interlaboratory comparison study for certification. A total of 21 selected expert laboratories from different European countries with documented expertise in the field of mycotoxin analysis took part in the certification study using various gas and liquid chromatographic methods. The certified values and their corresponding expanded uncertainties (k = 2) were assigned in full compliance with the requirements of ISO Guide 35 and are as follows: 102 ± 11 μg kg(-1) for DON, 1000 ± 130 μg kg(-1) for NIV and 90 ± 8 μg kg(-1) for ZEN.

  3. Results of a Saxitoxin Proficiency Test Including Characterization of Reference Material and Stability Studies.

    PubMed

    Harju, Kirsi; Rapinoja, Marja-Leena; Avondet, Marc-André; Arnold, Werner; Schär, Martin; Luginbühl, Werner; Kremp, Anke; Suikkanen, Sanna; Kankaanpää, Harri; Burrell, Stephen; Söderström, Martin; Vanninen, Paula

    2015-11-25

    A saxitoxin (STX) proficiency test (PT) was organized as part of the Establishment of Quality Assurance for the Detection of Biological Toxins of Potential Bioterrorism Risk (EQuATox) project. The aim of this PT was to provide an evaluation of existing methods and the European laboratories' capabilities for the analysis of STX and some of its analogues in real samples. Homogenized mussel material and algal cell materials containing paralytic shellfish poisoning (PSP) toxins were produced as reference sample matrices. The reference material was characterized using various analytical methods. Acidified algal extract samples at two concentration levels were prepared from a bulk culture of PSP toxins producing dinoflagellate Alexandrium ostenfeldii. The homogeneity and stability of the prepared PT samples were studied and found to be fit-for-purpose. Thereafter, eight STX PT samples were sent to ten participating laboratories from eight countries. The PT offered the participating laboratories the possibility to assess their performance regarding the qualitative and quantitative detection of PSP toxins. Various techniques such as official Association of Official Analytical Chemists (AOAC) methods, immunoassays, and liquid chromatography-mass spectrometry were used for sample analyses.

  4. Development of apple certified reference material for quantification of organophosphorus and pyrethroid pesticides.

    PubMed

    Otake, Takamitsu; Yarita, Takashi; Aoyagi, Yoshie; Kuroda, Youko; Numata, Masahiko; Iwata, Hitoshi; Watai, Masatoshi; Mitsuda, Hitoshi; Fujikawa, Takashi; Ota, Hidekazu

    2013-06-01

    An apple certified reference material for the analysis of pesticide residues was issued by the National Metrology Institute of Japan. Organophosphorus and pyrethroid pesticides were sprayed on apples, and these were used as raw materials of certified reference material. The harvested apples were cut into small pieces, freeze-dried, pulverized, sieved, placed into 200 brown glass bottles (3g each), and sterilized by γ-irradiation. Stability and homogeneity assessment was performed, and the relative uncertainties due to instability (for an expiry date of 32 months) and inhomogeneity were 10.3-25.0% and 4.0-6.8%, respectively. The characterization was carried out using multiple analytical methods to ensure the reliability of analytical results; the values of target pesticides were obtained by isotope dilution mass spectrometry. Certified values were 2.28 ± 0.82 mg/kg for diazinon, 3.14 ± 0.79 mg/kg for fenitrothion, 1.55 ± 0.81 mg/kg for cypermethrin, and 2.81 ± 0.70 mg/kg for permethrin.

  5. Evaluation of a fungal collection as certified reference material producer and as a biological resource center.

    PubMed

    Forti, Tatiana; Souto, Aline da S S; do Nascimento, Carlos Roberto S; Nishikawa, Marilia M; Hubner, Marise T W; Sabagh, Fernanda P; Temporal, Rosane Maria; Rodrigues, Janaína M; da Silva, Manuela

    2016-01-01

    Considering the absence of standards for culture collections and more specifically for biological resource centers in the world, in addition to the absence of certified biological material in Brazil, this study aimed to evaluate a Fungal Collection from Fiocruz, as a producer of certified reference material and as Biological Resource Center (BRC). For this evaluation, a checklist based on the requirements of ABNT ISO GUIA34:2012 correlated with the ABNT NBR ISO/IEC17025:2005, was designed and applied. Complementing the implementation of the checklist, an internal audit was performed. An evaluation of this Collection as a BRC was also conducted following the requirements of the NIT-DICLA-061, the Brazilian internal standard from Inmetro, based on ABNT NBR ISO/IEC 17025:2005, ABNT ISO GUIA 34:2012 and OECD Best Practice Guidelines for BRCs. This was the first time that the NIT DICLA-061 was applied in a culture collection during an internal audit. The assessments enabled the proposal for the adequacy of this Collection to assure the implementation of the management system for their future accreditation by Inmetro as a certified reference material producer as well as its future accreditation as a Biological Resource Center according to the NIT-DICLA-061. PMID:26991280

  6. The determination of water in crude oil and transformer oil reference materials.

    PubMed

    Margolis, Sam A; Hagwood, Charles

    2003-05-01

    The measurement of the amount of water in oils is of significant economic importance to the industrial community, particularly to the electric power and crude oil industries. The amount of water in transformer oils is critical to their normal function and the amount of water in crude oils affects the cost of the crude oil at the well head, the pipeline, and the refinery. Water in oil Certified Reference Materials (CRM) are essential for the accurate calibration of instruments that are used by these industries. Three NIST Standard Reference Materials (SRMs) have been prepared for this purpose. The water in these oils has been measured by both coulometric and volumetric Karl Fischer methods. The compounds (such as sulfur compounds) that interfere with the Karl Fischer reaction (interfering substances) and inflate the values for water by also reacting with iodine have been measured coulometrically. The measured water content of Reference Material (RM) 8506a Transformer Oil is 12.1+/-1.9 mg kg(-1) (plus an additional 6.2+/-0.9 mg kg(-1) of interfering substances). The measured water content of SRM 2722 Sweet Crude Oil, is 99+/-6 mg kg(-1) (plus an additional 5+/-2 mg kg(-1) of interfering substances). The measured water content of SRM 2721 Sour Crude Oil, is 134+/-18 mg kg(-1) plus an additional 807+/-43 mg kg(-1) of interfering substances. Interlaboratory studies conducted with these oil samples (using SRM 2890, water saturated 1-octanol, as a calibrant) are reported. Some of the possible sources of bias in these measurements were identified, These include: improperly calibrated instruments, inability to measure the calibrant accurately, Karl Fischer reagent selection, and volatilization of the interfering substances in SRM 2721.

  7. Preparation and certification of Re-Os dating reference materials: Molybdenites HLP and JDC

    USGS Publications Warehouse

    Du, A.; Wu, S.; Sun, D.; Wang, Shaoming; Qu, W.; Markey, R.; Stain, H.; Morgan, J.; Malinovskiy, D.

    2004-01-01

    Two Re-Os dating reference material molybdenites were prepared. Molybdenite JDC and molybdenite HLP are from a carbonate vein-type molybdenum-(lead)- uranium deposit in the Jinduicheng-Huanglongpu area of Shaanxi province, China. The samples proved to be homogeneous, based on the coefficient of variation of analytical results and an analysis of variance test. The sampling weight was 0.1 g for JDC and 0.025 g for HLP. An isotope dilution method was used for the determination of Re and Os. Sample decomposition and preconcentration of Re and Os prior to measurement were accomplished using a variety of methods: acid digestion, alkali fusion, ion exchange and solvent extraction. Negative thermal ionisation mass spectrometry and inductively coupled plasma-mass spectrometry were used for the determination of Re and 187Os concentration and isotope ratios. The certified values include the contents of Re and Os and the model ages. For HLP, the Re content was 283.8 ?? 6.2 ??g g-1, 187Os was 659 ?? 14 ng g-1 and the Re-Os model age was 221.4 ?? 5.6 Ma. For JDC, the Re content was 17.39 ?? 0.32 ng g-1, 187Os was 25.46 ?? 0.60 ng g-1 and the Re-Os model age was 139.6 ?? 3.8 Ma. Uncertainties for both certified reference materials are stated at the 95% level of confidence. Three laboratories (from three countries: P.R. China, USA, Sweden) joined in the certification programme. These certified reference materials are primarily useful for Re-Os dating of molybdenite, sulfides, black shale, etc.

  8. Effect of platform, reference material, and quantification model on enumeration of Enterococcus by quantitative PCR methods.

    PubMed

    Cao, Yiping; Sivaganesan, Mano; Kinzelman, Julie; Blackwood, A Denene; Noble, Rachel T; Haugland, Richard A; Griffith, John F; Weisberg, Stephen B

    2013-01-01

    Quantitative polymerase chain reaction (qPCR) is increasingly being used for the quantitative detection of fecal indicator bacteria in beach water. QPCR allows for same-day health warnings, and its application is being considered as an option for recreational water quality testing in the United States (USEPA, 2011. EPA-OW-2011-0466, FRL-9609-3, Notice of Availability of Draft Recreational Water Quality Criteria and Request for Scientific Views). However, transition of qPCR from a research tool to routine water quality testing requires information on how various method variations affect target enumeration. Here we compared qPCR performance and enumeration of enterococci in spiked and environmental water samples using three qPCR platforms (Applied Biosystem StepOnePlus™, the BioRad iQ™5 and the Cepheid SmartCycler(®) II), two reference materials (lyophilized cells and frozen cells on filters) and two comparative CT quantification models (ΔCT and ΔΔCT). Reference materials exerted the biggest influence, consistently affecting results by approximately 0.5 log(10) unit. Platform had the smallest effect, generally exerting <0.1 log(10) unit difference in final results. Quantification model led to small differences (0.04-0.2 log(10) unit) in this study with relatively uninhibited samples, but has the potential to cause as much as 8-fold (0.9 log(10) unit) difference in potentially inhibitory samples. Our findings indicate the need for a certified and centralized source of reference materials and additional studies to assess applicability of the quantification models in analyses of PCR inhibitory samples.

  9. Development of a standard reference material for Cr(vi) in contaminated soil

    USGS Publications Warehouse

    Nagourney, S.J.; Wilson, S.A.; Buckley, B.; Kingston, H.M.S.; Yang, S.-Y.; Long, S.E.

    2008-01-01

    Over the last several decades, considerable contamination by hexavalent chromium has resulted from the land disposal of Chromite Ore Processing Residue (COPR). COPR contains a number of hexavalent chromium-bearing compounds that were produced in high temperature industrial processes. Concern over the carcinogenic potential of this chromium species, and its environmental mobility, has resulted in efforts to remediate these waste sites. To provide support to analytical measurements of hexavalent chromium, a candidate National Institute of Standards and Technology (NIST) Standard Reference Material?? (SRM 2701), having a hexavalent chromium content of approximately 500 mg kg -1, has been developed using material collected from a waste site in Hudson County, New Jersey, USA. The collection, processing, preparation and preliminary physico-chemical characterization of the material are discussed. A two-phase multi-laboratory testing study was carried out to provide data on material homogeneity and to assess the stability of the material over the duration of the study. The study was designed to incorporate several United States Environmental Protection Agency (USEPA) determinative methods for hexavalent chromium, including Method 6800 which is based on speciated isotope dilution mass spectrometry (SIDMS), an approach which can account for chromium species inter-conversion during the extraction and measurement sequence. This journal is ?? The Royal Society of Chemistry 2008.

  10. Evaluation of the sulfur isotopic composition and homogeneity of the Soufre de Lacq reference material

    USGS Publications Warehouse

    Carmody, R.W.; Seal, R.R., II

    1999-01-01

    Sulfur isotopic analysis of the elemental sulfur reference material Soufre de Lacq, prepared as silver sulfide by chromous chloride reduction and as copper sulfide by sealed-tube synthesis, indicates that Soufre de Lacq is isotopically homogeneous across different size fractions to within analytical uncertainty (??0.15???). The sulfur isotopic composition of aliquots of Soufre de Lacq prepared by these two techniques are identical to within analytical uncertainty. The mean sulfur isotopic composition for Soufre de Lacq prepared as silver sulfide and copper sulfide (relative to VCDT) is +16.20 ?? 0.15??? (1??).

  11. Standard wool fabric as a reference material. [for fire toxicity tests

    NASA Technical Reports Server (NTRS)

    Hilado, C. J.; Cumming, H. J.

    1977-01-01

    Standard wool fabric is investigated as a potential reference material. A screening test method for relative toxicity exposes four albino male rats enclosed in a 4.2 liter hemispherical chamber to pyrolysis effluents produced by pyrolyzing a 1.00 g sample under a variety of test conditions (200-800 C with a 40 C/min heating rate). It is found that for fabrics containing 86-100% wool, animal response remains virtually unchanged, although a 100% wool fabric is preferred as it eliminates local composition differences as a source of variation.

  12. The Enigmatic Longevity of Granular Materials on Mars: The Case for Geologically Episodic Dune Formation

    NASA Technical Reports Server (NTRS)

    Marshall, J.

    1999-01-01

    Martian sand dunes are concentrated in vast sand seas in the circumpolar belt of the planet's northern hemisphere, but they are also pervasive over the whole planet. Their occurrence is to be expected on a super-arid planetary surface subjected to boundary layer drag from a continually active atmosphere. Whilst their occurrence is to be expected, their survival is enigmatic. But the enigma only arises if the martian system is considered similar to Earth's --where sand is moved highly frequently, more or less on a seasonal basis. Experimentally it is readily demonstrated that active sand will soon wear down to small grains and eventually diminish to below the critical sand size required to sustain dune formation. According to conventional wisdom, sand moves at higher speeds on Mars than on Earth, and if it were to move as frequently as it does on Earth, then the dune-forming sand population should have long since disappeared, given the great longevity of the martian aeolian system (Sagan coined the term "kamikaze" grains to express this disappearance). No supply of sand could keep pace with this depletion, especially in light of the fact that Mars does not have very active weathering, nor significant crustal differentiation. On Earth, plate tectonics, magmatic activity, and general crustal differentiation over geological time have produced great concentrations of quartz crystals in the continental crustal masses. Not only are these quartz grains chemically and mechanically resilient, they are about the right size for being transported by either wind or water. Add to this, the geologically recent contribution of glacial grinding, and it is easy to see why there are dune field on Earth. So what are the martian dunes composed of, and how does the material survive the eons of attrition? In addition to experimental demonstrations of sand comminution in laboratory aeolian simulations, the problem can be approached from first principles. Sagan showed that by simple

  13. Full-Vector, Low-Temperature Magnetic Measurements of Geologic Materials

    NASA Astrophysics Data System (ADS)

    Feinberg, J.; Sølheid, P.; Bowles, J. A.; Jackson, M. J.; Moskowitz, B. M.

    2010-12-01

    The magnetic properties of geologic materials offer insights into an enormous range of important geophysical phenomena ranging from core dynamics to paleoclimate. Low-temperature (<300 K) magnetic behavior can indicate the dominant magnetic mineral phases in a sample, determine the grain size distribution of the constituent magnetic minerals, and even reveal evidence of biogenic iron minerals. Low-temperature cycling across the magnetite Verwey transition is sometimes used to remove remanence associated with multi-domain grains, which is undesirable for paleointensity and other paleomagnetic experiments. Despite the utility of low-temperature magnetic data, probing these low-temperature phenomena from the perspective of understanding the underlying physical behavior has been hampered by instrumental limitations. Until now, nearly all measurements of low-temperature magnetization have been single-axis and are rarely done in true zero-field environments. Low-temperature remanence measurements at the Institute for Rock Magnetism (IRM) have been carried out almost exclusively on the Quantum Designs Magnetic Properties Measurement System (MPMS) where magnetization is measured only in the vertical direction, and “zero-fields” of up to 1 μT are common. The IRM - with funding from the Instrumentation and Facilities Program of the National Science Foundation, Earth Science Division, and in conjunction with ColdEdge Technologies (Allentown, Pennsylvania) - is developing a low-cost, cryogenic insert designed to work with a standard, horizontal-loading, 2G Enterprises magnetometer. Full three-axis measurements may now be made in ultra-low-field environments (nT) from ~17 K to room temperature. The design is compatible with both the large (7.6 cm) and small (4.2 cm) bore magnetometers, as well as many standard pulse magnetizers. Used in conjunction with the in-line degausser on the IRM’s pass-through magnetometer, it will ultimately be possible to acquire anhysteretic

  14. Spark ablation-inductively coupled plasma spectrometry for analysis of geologic materials

    USGS Publications Warehouse

    Golightly, D.W.; Montaser, A.; Smith, B.L.; Dorrzapf, A.F.

    1989-01-01

    Spark ablation-inductively coupled plasma (SA-ICP) spectrometry is applied to the measurement of hafnium-zirconium ratios in zircons and to the determination of cerium, cobalt, iron, lead, nickel and phosphorus in ferromanganese nodules. Six operating parameters used for the high-voltage spark and argon-ICP combination are established by sequential simplex optimization of both signal-to-background ratio and signal-to-noise ratio. The time-dependences of the atomic emission signals of analytes and matrix elements ablated from a finely pulverized sample embedded in a pressed disk of copper demonstrate selective sampling by the spark. Concentration ratios of hafnium to zirconium in zircons are measured with a precision of 4% (relative standard deviation, RSD). For ferromanganese nodules, spectral measurements based on intensity ratios of analyte line to the Mn(II) 257.610 nm line provide precisions of analysis in the range from 7 to 14% RSD. The accuracy of analysis depends on use of standard additions of the reference material USGS Nod P-1, and an independent measurement of the Mn concentration. ?? 1989.

  15. Certified Reference Material IAEA-446 for radionuclides in Baltic Sea seaweed.

    PubMed

    Pham, M K; Benmansour, M; Carvalho, F P; Chamizo, E; Degering, D; Engeler, C; Gascó, C; Gwynn, J P; Harms, A V; Hrnecek, E; Ibanez, F L; Ilchmann, C; Ikaheimonen, T; Kanisch, G; Kloster, M; Llaurado, M; Mauring, A; Møller, B; Morimoto, T; Nielsen, S P; Nies, H; Norrlid, L D R; Pettersson, H B L; Povinec, P P; Rieth, U; Samuelsson, C; Schikowski, J; Silobritiene, B V; Smedley, P A; Suplinska, M; Vartti, V-P; Vasileva, E; Wong, J; Zalewska, T; Zhou, W

    2014-05-01

    A Certified Reference Material (CRM) for radionuclides in seaweed (Fucus vesiculosus) from the Baltic Sea (IAEA-446) is described and the results of the certification process are presented. The (40)K, (137)Cs, (234)U and (239+240)Pu radionuclides were certified for this material, and information values for 12 other radionuclides ((90)Sr, (99)Tc, (210)Pb ((210)Po), (226)Ra, (228)Ra, (228)Th, (230)Th, (232)Th, (235)U, (238)U, (239)Pu and (240)Pu) are presented. The CRM can be used for Quality Assurance/Quality Control of analysis of radionuclides in seaweed and other biota samples, as well as for development and validation of analytical methods, and for training purposes.

  16. Certified Reference Material IAEA-446 for radionuclides in Baltic Sea seaweed.

    PubMed

    Pham, M K; Benmansour, M; Carvalho, F P; Chamizo, E; Degering, D; Engeler, C; Gascó, C; Gwynn, J P; Harms, A V; Hrnecek, E; Ibanez, F L; Ilchmann, C; Ikaheimonen, T; Kanisch, G; Kloster, M; Llaurado, M; Mauring, A; Møller, B; Morimoto, T; Nielsen, S P; Nies, H; Norrlid, L D R; Pettersson, H B L; Povinec, P P; Rieth, U; Samuelsson, C; Schikowski, J; Silobritiene, B V; Smedley, P A; Suplinska, M; Vartti, V-P; Vasileva, E; Wong, J; Zalewska, T; Zhou, W

    2014-05-01

    A Certified Reference Material (CRM) for radionuclides in seaweed (Fucus vesiculosus) from the Baltic Sea (IAEA-446) is described and the results of the certification process are presented. The (40)K, (137)Cs, (234)U and (239+240)Pu radionuclides were certified for this material, and information values for 12 other radionuclides ((90)Sr, (99)Tc, (210)Pb ((210)Po), (226)Ra, (228)Ra, (228)Th, (230)Th, (232)Th, (235)U, (238)U, (239)Pu and (240)Pu) are presented. The CRM can be used for Quality Assurance/Quality Control of analysis of radionuclides in seaweed and other biota samples, as well as for development and validation of analytical methods, and for training purposes. PMID:24291528

  17. Fundamental studies to develop certified reference material to calibrate spectrophotometer in the ultraviolet region

    NASA Astrophysics Data System (ADS)

    da Conceição, F. C.; Borges, P. P.; Gomes, J. F. S.

    2016-07-01

    Spectrophotometry is the technique used in a great number of laboratories around the world. Quantitative determination of a high number of inorganic, organic and biological species can be made by spectrophotometry using calibrated spectrophotometers. International standards require the use of optical filters to perform the calibration of spectrophotometers. One of the recommended materials is the crystalline potassium dichromate (K2Cr2O7), which is used to prepare solutions in specific concentrations for calibration or verification of spectrophotometers in the ultraviolet (UV) spectral regions. This paper presents the results concerning the fundamental studies for developing a certified reference material (CRM) of crystalline potassium dichromate to be used as standard of spectrophotometers in order to contribute to reliable quantitative analyses.

  18. Aflatoxin M1 in milk powders: processing, homogeneity and stability testing of certified reference materials.

    PubMed

    Josephs, R D; Ulberth, F; Van Egmond, H P; Emons, H

    2005-09-01

    As part of the certification campaign of three candidate reference materials for the determination of aflatoxin M1 (AfM1) in whole milk powders, homogeneity, short- and long-term stability tests of naturally contaminated milk powders have been performed. The homogeneity of two AfM1-contaminated milk powders was studied by taking samples at regular intervals of the filling sequences and analysing in triplicate for their AfM1 contents by liquid chromatography with fluorescence detection (LC-FLD) using random stratified sampling schemes. The homogeneity testing of an AfM1 'blank' milk powder material was performed by determining the nitrogen content because AfM1 levels were below the limit of detection of the most sensitive determination method. The short-term stability of AfM1-contaminated milk powders was evaluated at three different storage temperatures (4, 18 and 40 degrees C). After storage times of 0, 1, 2 and 4 weeks, samples were investigated using LC-FLD. The long-term stability study comprised of measurements after 0, 6, 12 and 18 months after storage at -20 and 4 degrees C. Analyses were done by LC-FLD. Based on the homogeneity tests, the materials were sufficiently homogenous to serve as certified reference materials. Corresponding uncertainty contributions of 0.23-0.89% were calculated for the homogeneity. The stability measurements showed no significant trends for both short- and long-term stability studies. The long-term stability uncertainties of the AfM1-contaminated milk powders were 7.4 and 6.3%, respectively, for a shelf-life of 6 years and storage at -20 degrees C. Supplementary stability monitoring schemes over a long period of several years are currently ongoing.

  19. Assessment of commutability for candidate certified reference material ERM-BB130 "chloramphenicol in pork".

    PubMed

    Zeleny, Reinhard; Emteborg, Håkan; Schimmel, Heinz

    2010-10-01

    Chloramphenicol (CAP), an effective antibiotic against many microorganisms, is meanwhile banned in the EU for treatment of food-producing animals due to adverse health effects. The Institute for Reference Materials and Measurements (IRMM) is currently developing a certified reference material (CRM) for CAP in pork, intended for validation and method performance verifications of analytical methods. The material will be certified using liquid chromatography-tandem mass spectrometry (LC-MS/MS) and gas chromatography-mass spectrometry (GC-MS) methods and has a target CAP level around the minimum required performance limit (MRPL) of 0.3 microg/kg. To prove that the material can be applied as a quality control tool for screening methods, a commutability study was conducted, involving five commercially available enzyme-linked immunosorbent assay kits and one biosensor assay (BiaCore kit). Meat homogenates (cryo-milled wet tissue) with CAP concentrations around the MRPL and the candidate CRM (lyophilised powder) were measured by LC-MS/MS and GC-MS as well as the six screening methods. Pairwise method comparisons of results obtained for the two sample types showed that the CRM can successfully be applied as quality control (QC) sample to all six screening methods. The study suggests that ERM-BB130 is sufficiently commutable with the investigated assays and that laboratories applying one of the investigated kits therefore benefit from using ERM-BB130 to demonstrate the correctness of their results. However, differences among the assays were observed, either in the abundance of bias between screening and confirmatory LC and GC methods, the repeatability of test results, or goodness of fit between the methods. PMID:20665007

  20. Utilizing a reference material for assessing absolute tumor mechanical properties in modality independent elastography

    NASA Astrophysics Data System (ADS)

    Kim, Dong Kyu; Weis, Jared A.; Yankeelov, Thomas E.; Miga, Michael I.

    2014-03-01

    There is currently no reliable method for early characterization of breast cancer response to neoadjuvant chemotherapy (NAC) [1,2]. Given that disruption of normal structural architecture occurs in cancer-bearing tissue, we hypothesize that further structural changes occur in response to NAC. Consequently, we are investigating the use of modalityindependent elastography (MIE) [3-8] as a method for monitoring mechanical integrity to predict long term outcomes in NAC. Recently, we have utilized a Demons non-rigid image registration method that allows 3D elasticity reconstruction in abnormal tissue geometries, making it particularly amenable to the evaluation of breast cancer mechanical properties. While past work has reflected relative elasticity contrast ratios [3], this study improves upon that work by utilizing a known stiffness reference material within the reconstruction framework such that a stiffness map becomes an absolute measure. To test, a polyvinyl alcohol (PVA) cryogel phantom and a silicone rubber mock mouse tumor phantom were constructed with varying mechanical stiffness. Results showed that an absolute measure of stiffness could be obtained based on a reference value. This reference technique demonstrates the ability to generate accurate measurements of absolute stiffness to characterize response to NAC. These results support that `referenced MIE' has the potential to reliably differentiate absolute tumor stiffness with significant contrast from that of surrounding tissue. The use of referenced MIE to obtain absolute quantification of biomarkers is also translatable across length scales such that the characterization method is mechanics-consistent at the small animal and human application.

  1. Geochemical Analyses of Geologic Materials from Areas of Critical Environmental Concern, Clark and Nye Counties, Nevada

    USGS Publications Warehouse

    Ludington, Steve; Castor, Stephen B.; Budahn, James R.; Flynn, Kathryn S.

    2005-01-01

    INTRODUCTION An assessment of known and undiscovered mineral resources of selected areas administered by the Bureau of Land Management (BLM) in Clark and Nye Counties, Nevada was conducted by the U.S. Geological Survey (USGS), Nevada Bureau of Mines and Geology (NBMG), and University of Nevada, Las Vegas (UNLV). The purpose of this work was to provide the BLM with information for use in their long-term planning process in southern Nevada so that they can make better-informed decisions. The results of the assessment are in Ludington (2006). Existing information about the areas, including geology, geophysics, geochemistry, and mineral-deposit information was compiled, and field examinations of selected areas and mineral occurrences was conducted. This information was used to determine the geologic setting, metallogenic characteristics, and mineral potential of the areas. Twenty-five Areas of Critical Environmental Concern (ACECs) were identified by BLM as the object of this study. They range from tiny (less than one km2) to large (more than 1,000 km2). The location of the study areas is shown on Figure 1. This report includes geochemical data for rock samples collected by staff of the USGS and NBMG in these ACECs and nearby areas. Samples have been analyzed from the Big Dune, Ash Meadows, Arden, Desert Tortoise Conservation Center, Coyote Springs Valley, Mormon Mesa, Virgin Mountains, Gold Butte A and B, Whitney Pockets, Rainbow Gardens, River Mountains, and Piute-Eldorado Valley ACECs.

  2. Accuracy of ELISA detection methods for gluten and reference materials: a realistic assessment.

    PubMed

    Diaz-Amigo, Carmen; Popping, Bert

    2013-06-19

    The determination of prolamins by ELISA and subsequent conversion of the resulting concentration to gluten content in food appears to be a comparatively simple and straightforward process with which many laboratories have years-long experience. At the end of the process, a value of gluten, expressed in mg/kg or ppm, is obtained. This value often is the basis for the decision if a product can be labeled gluten-free or not. On the basis of currently available scientific information, the accuracy of the obtained values with commonly used commercial ELISA kits has to be questioned. Although recently several multilaboratory studies have been conducted in an attempt to emphasize and ensure the accuracy of the results, data suggest that it was the precision of these assays, not the accuracy, that was confirmed because some of the underlying assumptions for calculating the gluten content lack scientific data support as well as appropriate reference materials for comparison. This paper discusses the issues of gluten determination and quantification with respect to antibody specificity, extraction procedures, reference materials, and their commutability.

  3. Soot Reference Materials for instrument calibration and intercomparisons: a workshop summary with recommendations

    NASA Astrophysics Data System (ADS)

    Baumgardner, D.; Popovicheva, O.; Allan, J.; Bernardoni, V.; Cao, J.; Cavalli, F.; Cozic, J.; Diapouli, E.; Eleftheriadis, K.; Genberg, P. J.; Gonzalez, C.; Gysel, M.; John, A.; Kirchstetter, T. W.; Kuhlbusch, T. A. J.; Laborde, M.; Lack, D.; Müller, T.; Niessner, R.; Petzold, A.; Piazzalunga, A.; Putaud, J. P.; Schwarz, J.; Sheridan, P.; Subramanian, R.; Swietlicki, E.; Valli, G.; Vecchi, R.; Viana, M.

    2012-03-01

    Soot, which is produced from biomass burning and the incomplete combustion of fossil and biomass fuels, has been linked to regional and global climate change and to negative health problems. Scientists measure soot using a variety of methods in order to quantify source emissions and understand its atmospheric chemistry, reactivity under emission conditions, interaction with solar radiation, influence on clouds, and health impacts. A major obstacle currently limiting progress is the absence of established standards or reference materials for calibrating the many instruments used to measure the various properties of soot. The current state of availability and practicability of soot standard reference materials (SRMs) was reviewed by a group of 50 international experts during a workshop in June of 2011. The workshop was convened to summarize the current knowledge on soot measurement techniques, identify the measurement uncertainties and limitations related to the lack of SRMs, and identify attributes of SRMs that, if developed, would reduce measurement uncertainties. The workshop established that suitable SRMs are available for calibrating some, but not all, measurement methods. The community of single-particle sootphotometer (SP2) users identified a suitable SRM, fullerene soot, but users of instruments that measure light absorption by soot collected on filters did not. Similarly, those who use thermal optical analysis (TOA) to analyze the organic and elemental carbon components of soot were not satisfied with current SRMs. The workshop produced recommendations for the development of new SRMs that would be suitable for the different soot measurement methods.

  4. Periodic reference tracking control approach for smart material actuators with complex hysteretic characteristics

    NASA Astrophysics Data System (ADS)

    Sun, Zhiyong; Hao, Lina; Song, Bo; Yang, Ruiguo; Cao, Ruimin; Cheng, Yu

    2016-10-01

    Micro/nano positioning technologies have been attractive for decades for their various applications in both industrial and scientific fields. The actuators employed in these technologies are typically smart material actuators, which possess inherent hysteresis that may cause systems behave unexpectedly. Periodic reference tracking capability is fundamental for apparatuses such as scanning probe microscope, which employs smart material actuators to generate periodic scanning motion. However, traditional controller such as PID method cannot guarantee accurate fast periodic scanning motion. To tackle this problem and to conduct practical implementation in digital devices, this paper proposes a novel control method named discrete extended unparallel Prandtl-Ishlinskii model based internal model (d-EUPI-IM) control approach. To tackle modeling uncertainties, the robust d-EUPI-IM control approach is investigated, and the associated sufficient stabilizing conditions are derived. The advantages of the proposed controller are: it is designed and represented in discrete form, thus practical for digital devices implementation; the extended unparallel Prandtl-Ishlinskii model can precisely represent forward/inverse complex hysteretic characteristics, thus can reduce modeling uncertainties and benefits controllers design; in addition, the internal model principle based control module can be utilized as a natural oscillator for tackling periodic references tracking problem. The proposed controller was verified through comparative experiments on a piezoelectric actuator platform, and convincing results have been achieved.

  5. Extensive sequencing of seven human genomes to characterize benchmark reference materials.

    PubMed

    Zook, Justin M; Catoe, David; McDaniel, Jennifer; Vang, Lindsay; Spies, Noah; Sidow, Arend; Weng, Ziming; Liu, Yuling; Mason, Christopher E; Alexander, Noah; Henaff, Elizabeth; McIntyre, Alexa B R; Chandramohan, Dhruva; Chen, Feng; Jaeger, Erich; Moshrefi, Ali; Pham, Khoa; Stedman, William; Liang, Tiffany; Saghbini, Michael; Dzakula, Zeljko; Hastie, Alex; Cao, Han; Deikus, Gintaras; Schadt, Eric; Sebra, Robert; Bashir, Ali; Truty, Rebecca M; Chang, Christopher C; Gulbahce, Natali; Zhao, Keyan; Ghosh, Srinka; Hyland, Fiona; Fu, Yutao; Chaisson, Mark; Xiao, Chunlin; Trow, Jonathan; Sherry, Stephen T; Zaranek, Alexander W; Ball, Madeleine; Bobe, Jason; Estep, Preston; Church, George M; Marks, Patrick; Kyriazopoulou-Panagiotopoulou, Sofia; Zheng, Grace X Y; Schnall-Levin, Michael; Ordonez, Heather S; Mudivarti, Patrice A; Giorda, Kristina; Sheng, Ying; Rypdal, Karoline Bjarnesdatter; Salit, Marc

    2016-06-07

    The Genome in a Bottle Consortium, hosted by the National Institute of Standards and Technology (NIST) is creating reference materials and data for human genome sequencing, as well as methods for genome comparison and benchmarking. Here, we describe a large, diverse set of sequencing data for seven human genomes; five are current or candidate NIST Reference Materials. The pilot genome, NA12878, has been released as NIST RM 8398. We also describe data from two Personal Genome Project trios, one of Ashkenazim Jewish ancestry and one of Chinese ancestry. The data come from 12 technologies: BioNano Genomics, Complete Genomics paired-end and LFR, Ion Proton exome, Oxford Nanopore, Pacific Biosciences, SOLiD, 10X Genomics GemCode WGS, and Illumina exome and WGS paired-end, mate-pair, and synthetic long reads. Cell lines, DNA, and data from these individuals are publicly available. Therefore, we expect these data to be useful for revealing novel information about the human genome and improving sequencing technologies, SNP, indel, and structural variant calling, and de novo assembly.

  6. Enantiomer fractions of polychlorinated biphenyls in three selected Standard Reference Materials.

    PubMed

    Morrissey, Joshua A; Bleackley, Derek S; Warner, Nicholas A; Wong, Charles S

    2007-01-01

    The enantiomer composition of six chiral polychlorinated biphenyls (PCBs) were measured in three different certified Standard Reference Materials (SRMs) from the US National Institute of Standards and Technology (NIST): SRM 1946 (Lake Superior fish tissue), SRM 1939a (PCB Congeners in Hudson River Sediment), and SRM 2978 (organic contaminants in mussel tissue--Raritan Bay, New Jersey) to aid in quality assurance/quality control methodologies in the study of chiral pollutants in sediments and biota. Enantiomer fractions (EFs) of PCBs 91, 95, 136, 149, 174, and 183 were measured using a suite of chiral columns by gas chromatography/mass spectrometry. Concentrations of target analytes were in agreement with certified values. Target analyte EFs in reference materials were measured precisely (<2% relative standard deviation), indicating the utility of SRM in quality assurance/control methodologies for analyses of chiral compounds in environmental samples. Measured EFs were also in agreement with previously published analyses of similar samples, indicating that similar enantioselective processes were taking place in these environmental matrices. PMID:16777177

  7. Extensive sequencing of seven human genomes to characterize benchmark reference materials.

    PubMed

    Zook, Justin M; Catoe, David; McDaniel, Jennifer; Vang, Lindsay; Spies, Noah; Sidow, Arend; Weng, Ziming; Liu, Yuling; Mason, Christopher E; Alexander, Noah; Henaff, Elizabeth; McIntyre, Alexa B R; Chandramohan, Dhruva; Chen, Feng; Jaeger, Erich; Moshrefi, Ali; Pham, Khoa; Stedman, William; Liang, Tiffany; Saghbini, Michael; Dzakula, Zeljko; Hastie, Alex; Cao, Han; Deikus, Gintaras; Schadt, Eric; Sebra, Robert; Bashir, Ali; Truty, Rebecca M; Chang, Christopher C; Gulbahce, Natali; Zhao, Keyan; Ghosh, Srinka; Hyland, Fiona; Fu, Yutao; Chaisson, Mark; Xiao, Chunlin; Trow, Jonathan; Sherry, Stephen T; Zaranek, Alexander W; Ball, Madeleine; Bobe, Jason; Estep, Preston; Church, George M; Marks, Patrick; Kyriazopoulou-Panagiotopoulou, Sofia; Zheng, Grace X Y; Schnall-Levin, Michael; Ordonez, Heather S; Mudivarti, Patrice A; Giorda, Kristina; Sheng, Ying; Rypdal, Karoline Bjarnesdatter; Salit, Marc

    2016-01-01

    The Genome in a Bottle Consortium, hosted by the National Institute of Standards and Technology (NIST) is creating reference materials and data for human genome sequencing, as well as methods for genome comparison and benchmarking. Here, we describe a large, diverse set of sequencing data for seven human genomes; five are current or candidate NIST Reference Materials. The pilot genome, NA12878, has been released as NIST RM 8398. We also describe data from two Personal Genome Project trios, one of Ashkenazim Jewish ancestry and one of Chinese ancestry. The data come from 12 technologies: BioNano Genomics, Complete Genomics paired-end and LFR, Ion Proton exome, Oxford Nanopore, Pacific Biosciences, SOLiD, 10X Genomics GemCode WGS, and Illumina exome and WGS paired-end, mate-pair, and synthetic long reads. Cell lines, DNA, and data from these individuals are publicly available. Therefore, we expect these data to be useful for revealing novel information about the human genome and improving sequencing technologies, SNP, indel, and structural variant calling, and de novo assembly. PMID:27271295

  8. Advances in Isotope Ratio Mass Spectrometry and Required Isotope Reference Materials

    PubMed Central

    Vogl, Jochen

    2013-01-01

    The article gives a condensed version of the keynote lecture held at the International Mass Spectrometry Conference 2012 in Kyoto. Starting with some examples for isotope research the key requirements for metrologically valid procedures enabling traceable and comparable isotope data are discussed. Of course multi-collector mass spectrometers are required which offer sufficiently high isotope ratio precision for the intended research work. Following this, corrections for mass fractionation/discrimination, validation of the analytical procedure including chemical sample preparation and complete uncertainty budgets are the most important issues for obtaining a metrologically valid procedure for isotope ratio determination. Only the application of such metrologically valid procedures enables the generation of traceable and comparable isotope data. To realize this suitable isotope and/or δ-reference materials are required, which currently are not sufficiently available for most isotope systems. Boron is given as an example, for which the situation regarding isotope and δ-reference materials is excellent. Boron may therefore serve as prototype for other isotope systems. PMID:24349939

  9. Determination of plutonium isotopes in seawater reference materials using isotope-dilution ICP-MS.

    PubMed

    Zheng, Jian; Yamada, Masatoshi

    2012-09-01

    We analyzed the activities of (239)Pu, (240)Pu, (239+240)Pu, (241)Pu, the ratio of number of atoms (atom ratio) for (240)Pu/(239)Pu, and the activity ratio of (241)Pu/(239+240)Pu in seawater reference materials, IAEA-443 and IAEA-381, using a highly sensitive isotope dilution sector field inductively coupled plasma mass spectrometry method. With a mean chemical yield of 65% determined with (242)Pu as a tracer, we found that the experimentally established values in IAEA-443 for (239)Pu, (240)Pu, (241)Pu and (239+240)Pu activities are almost the same as those in IAEA-381. Regarding the (239+240)Pu activity, we provided the most precise and accurate result among the twelve laboratories, which participated in the interlaboratory comparison. In addition, for the (240)Pu/(239)Pu atom ratio, our results for IAEA-381 (0.2315±0.0008) and IAEA-443 (0.2325±0.0008) are in good agreement with the IAEA information value (0.229±0.006), but have much smaller uncertainty. Since the new seawater reference material, IAEA-443, is commercially available, it can be used not only for method validation for seawater plutonium isotope ratio and activity analysis, but also for more general use as a plutonium isotope standard for mass discrimination correction for other environmental samples.

  10. Extensive sequencing of seven human genomes to characterize benchmark reference materials

    PubMed Central

    Zook, Justin M.; Catoe, David; McDaniel, Jennifer; Vang, Lindsay; Spies, Noah; Sidow, Arend; Weng, Ziming; Liu, Yuling; Mason, Christopher E.; Alexander, Noah; Henaff, Elizabeth; McIntyre, Alexa B.R.; Chandramohan, Dhruva; Chen, Feng; Jaeger, Erich; Moshrefi, Ali; Pham, Khoa; Stedman, William; Liang, Tiffany; Saghbini, Michael; Dzakula, Zeljko; Hastie, Alex; Cao, Han; Deikus, Gintaras; Schadt, Eric; Sebra, Robert; Bashir, Ali; Truty, Rebecca M.; Chang, Christopher C.; Gulbahce, Natali; Zhao, Keyan; Ghosh, Srinka; Hyland, Fiona; Fu, Yutao; Chaisson, Mark; Xiao, Chunlin; Trow, Jonathan; Sherry, Stephen T.; Zaranek, Alexander W.; Ball, Madeleine; Bobe, Jason; Estep, Preston; Church, George M.; Marks, Patrick; Kyriazopoulou-Panagiotopoulou, Sofia; Zheng, Grace X.Y.; Schnall-Levin, Michael; Ordonez, Heather S.; Mudivarti, Patrice A.; Giorda, Kristina; Sheng, Ying; Rypdal, Karoline Bjarnesdatter; Salit, Marc

    2016-01-01

    The Genome in a Bottle Consortium, hosted by the National Institute of Standards and Technology (NIST) is creating reference materials and data for human genome sequencing, as well as methods for genome comparison and benchmarking. Here, we describe a large, diverse set of sequencing data for seven human genomes; five are current or candidate NIST Reference Materials. The pilot genome, NA12878, has been released as NIST RM 8398. We also describe data from two Personal Genome Project trios, one of Ashkenazim Jewish ancestry and one of Chinese ancestry. The data come from 12 technologies: BioNano Genomics, Complete Genomics paired-end and LFR, Ion Proton exome, Oxford Nanopore, Pacific Biosciences, SOLiD, 10X Genomics GemCode WGS, and Illumina exome and WGS paired-end, mate-pair, and synthetic long reads. Cell lines, DNA, and data from these individuals are publicly available. Therefore, we expect these data to be useful for revealing novel information about the human genome and improving sequencing technologies, SNP, indel, and structural variant calling, and de novo assembly. PMID:27271295

  11. Modeling and Analysis of Scatterometry Signatures for Optical Critical Dimension Reference Material Applications

    NASA Astrophysics Data System (ADS)

    Patrick, Heather J.; Germer, Thomas A.; Cresswell, Michael W.; Allen, Richard A.; Dixson, Ronald G.; Bishop, Michael

    2007-09-01

    We use an optical critical dimension (OCD) technique, matching modeled to measured scatterometry signatures, to obtain critical dimension linewidth of lines in grating targets fabricated on SIMOX (separation by implantation of oxygen) substrates using the single-crystal critical dimension reference materials (SCCDRM) process. We first compare experimentally obtained reflectance signatures for areas of the unpatterned substrate with signatures modeled using Fresnel theory, and show that the buried oxide (BOX) layer of the SIMOX is not well described optically by a single homogeneous layer of SiO2, but can be so described if a mixed Si-SiO2 boundary layer is included between the Si wafer and the BOX layer. We then obtain linewidths from OCD measurements on a series of grating targets with a range of design linewidths and pitches, and show that the linewidth obtained from the OCD technique is linearly related to the linewidth obtained from scanning electron microscopy (SEM), with a slope near unity and zero offset. While these results are very promising, further work in improving the fit of the simulated signatures to the measured signatures for some of the targets, reducing the target line roughness, and analyzing the uncertainties for potential optical critical dimension reference materials, is anticipated.

  12. Production of NDA Working Reference Materials for the Capability Evaluation Project

    SciTech Connect

    Noll, P.D. Jr.; Marshall, R.S.

    1998-11-17

    The production of Non Destructive Assay (NDA) Working Reference Materials (WRMs) that are traceable to nationally recognized standards was undertaken to support implementation of the Idaho National Engineering and Environmental Laboratory (INEEL) Nondestructive Waste Assay Capability Evaluation Project (CEP). The WRMs produced for the CEP project consist of Increased Am/Pu mass ration (IAP) and depleted Uranium (DU) WRMs. The CEP IAP/DU WRM set provides radioactive material standards for use in combination with 55 gallon drum waste matrix surrogates for the assessment of waste NDA assay system performance. The Production of WRMs is a meticulous process that is not without certain trials and tribulations. Problems may arise at any of the various stages of WRM production which include, but are not limited to; material characterization (physical, chemical, and isotopic), material blend parameters, personnel radiation exposure, gas generation phenomenon, traceability to national standards, encapsulation, statistical evaluation of the data, and others. Presented here is an overall description of the process by which the CEP WRMs were produced and certified as well as discussions pertaining to some of the problems encountered and how they were solved.

  13. Geologic Time.

    ERIC Educational Resources Information Center

    Albritton, Claude C., Jr.

    1984-01-01

    Discusses the historical development of the concept of geologic time. Develops the topic by using the major discoveries of geologists, beginning with Steno and following through to the discovery and use of radiometric dating. An extensive reference list is provided. (JM)

  14. High concentration aqueous sodium fluoride certified reference materials for forensic use certified by complexometric titration.

    PubMed

    Archer, Marcellé; Brits, Martin; Prevoo-Franzsen, Désirée; Quinn, Laura

    2015-04-01

    Sodium fluoride in concentrations of 1 to 2 % is used to prevent the formation of ethanol in blood and urine samples that are to be analysed for ethanol content. The majority of such samples form part of forensic investigations into alleged drunken driving. In South Africa, the laboratory performing the tests is required to prove that the sodium fluoride concentration in the blood samples is above 1 g/100 ml on receipt. This is done by using a fluoride ion-selective electrode calibrated with external aqueous solutions of sodium fluoride. The National Metrology Institute of South Africa (NMISA) prepares sodium fluoride solutions in concentrations from 0.3 to 3.0 g/100 ml. No other certified sodium fluoride reference solutions in these concentrations are available commercially. The sodium fluoride is certified by precipitation of the fluoride as lead chlorofluoride (PbClF) through the addition of a known excess of lead nitrate. The excess lead is back-titrated with ethylenediamine tetraacetic acid (EDTA) using a photometric electrode to detect the endpoint. Aqueous sodium fluoride solutions are prepared and the concentrations verified by the precipitation/back-titration method. This paper shows the application of a classical complexometric method to the certification of reference materials and describes the procedures for the preparation of the sodium fluoride solutions, verification of the concentrations, homogeneity and stability by primary titrimetry. It also briefly covers the calculation of uncertainty, the establishment of traceability and the quality control measures applied to ensure the quality of the certified reference materials (CRMs). PMID:25326884

  15. High concentration aqueous sodium fluoride certified reference materials for forensic use certified by complexometric titration.

    PubMed

    Archer, Marcellé; Brits, Martin; Prevoo-Franzsen, Désirée; Quinn, Laura

    2015-04-01

    Sodium fluoride in concentrations of 1 to 2 % is used to prevent the formation of ethanol in blood and urine samples that are to be analysed for ethanol content. The majority of such samples form part of forensic investigations into alleged drunken driving. In South Africa, the laboratory performing the tests is required to prove that the sodium fluoride concentration in the blood samples is above 1 g/100 ml on receipt. This is done by using a fluoride ion-selective electrode calibrated with external aqueous solutions of sodium fluoride. The National Metrology Institute of South Africa (NMISA) prepares sodium fluoride solutions in concentrations from 0.3 to 3.0 g/100 ml. No other certified sodium fluoride reference solutions in these concentrations are available commercially. The sodium fluoride is certified by precipitation of the fluoride as lead chlorofluoride (PbClF) through the addition of a known excess of lead nitrate. The excess lead is back-titrated with ethylenediamine tetraacetic acid (EDTA) using a photometric electrode to detect the endpoint. Aqueous sodium fluoride solutions are prepared and the concentrations verified by the precipitation/back-titration method. This paper shows the application of a classical complexometric method to the certification of reference materials and describes the procedures for the preparation of the sodium fluoride solutions, verification of the concentrations, homogeneity and stability by primary titrimetry. It also briefly covers the calculation of uncertainty, the establishment of traceability and the quality control measures applied to ensure the quality of the certified reference materials (CRMs).

  16. Free aluminium extraction from various reference materials and acid soils with relation to plant availability.

    PubMed

    Matús, Peter; Kubová, Jana; Bujdos, Marek; Medved', Ján

    2006-12-15

    The single extractions with 15 extractants (agents) (H(2)O, KCl, NH(4)Cl, NH(4)F, CaCl(2), BaCl(2), CuCl(2), LaCl(3), Na(2)S(2)O(4), (NH(4))(2)C(2)O(4), Na(4)P(2)O(7), NTA, EDTA, DTPA, HCl), the optimised BCR (Community Bureau of Reference) three-step sequential extraction procedure (SEP) and the solid phase extraction (SPE) by the chelating ion-exchanger Iontosorb Salicyl (cellulose resin containing covalently bound salicylic acid functional groups) were used for the partitioning of Al in very acid soil samples taken from an area influenced by acid mine solutions. The precision, accuracy and repeatibility for all steps of the optimised BCR SEP were checked on the various reference materials (CRM 483 sewage sludge amended soil, CRM BCR 701 freshwater sediment, SRM 2710 and SRM 2711 Montana soils). Also the new indicative values of the optimised BCR SEP fractional Al concentrations were obtained for these reference materials. The aluminium amounts obtained by the used extraction procedures were valuated and discussed from the aspect of the Al concentration in the plants (grass) growing on the same studied soils. The aluminium toxicity indexes (ATI) calculated for the studied soils, the BaCl(2) and acetic acid soil extracts and the grass stems and roots were used for the assessment of the Al toxicity to the plants. The ATI value was defined as the ratio of the nutrient cations (Ca, Mg, K, Na) concentration sum to the Al concentration. The flame atomic absorption spectrometry (LOQ=0.2mgl(-1)) and the inductively coupled plasma optical emission spectrometry (LOQ=0.03mgl(-1)) were used for the aluminium quantification. PMID:18970873

  17. Production of trace elements in coastal sea water certified reference material NMIA MX014.

    PubMed

    Merrick, Jeffrey P; Saxby, David L; White, Ian E A W; Antin, Luminita; Murby, E John

    2016-06-01

    A certified reference material (CRM) for trace elements in acidified sea water, NMIA MX014, has been produced by the National Measurement Institute Australia (NMIA). The CRM consists of natural coastal sea water with 12 elements (As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Se and V) fortified to levels relevant to environmental regulatory testing in Australia ranging from 0.4 to 22 μg/kg. Certified values for these 12 elements were assigned using reference methods developed at NMIA, using either isotope dilution or standard addition with ICP-MS measurement. Specialised sample preparation (coprecipitation) and ICP-MS optimisation (online dilution, collision/reaction chemistry, high mass resolution) were used to negate the effect of the high level of dissolved solids. Multiple confirmatory experiments were performed in order to verify that ICP-MS spectral interferences were eliminated and to estimate the measurement uncertainty contribution from method precision and method trueness. Extensive homogeneity and stability testing was performed and the measurement uncertainty of certified values includes contributions from between-bottle homogeneity, short-term stability, medium-term stability and long-term stability. Special attention was paid to the stability of Hg due to well-known preservation problems. Acidified sea water matrix was satisfactory for stabilising Hg at 0.4 μg/kg for at least 4 years. Relative expanded uncertainties (k = 2) for the 12 certified values were between 1 and 11 %. NMIA MX014 is intended for use as a reference material for analytical method validation and quality control for quantification of trace elements in saline water and other similar sample types. PMID:27108283

  18. A technical review of the feasibility of producing certified reference materials for the measurement of gaseous pollutants in ambient air

    NASA Astrophysics Data System (ADS)

    Hafkenscheid, Theo; Baldan, Annarita; Quincey, Paul; Cortez, Leopoldo; Dias, Florbela; Brown, Richard H.; Wright, Mike; Gerboles, Michel; Saunders, Kevin

    Within the frame of the EU sponsored project 'Cermatair' (Certified Reference Materials for the Measurement of Gaseous Pollutants in Ambient Air, contract G6RD-CT-2001-00517) the feasibility of preparing and certifying reference materials for the measurement of sulphur dioxide, nitrogen dioxide, carbon monoxide and benzene in ambient air was studied. The project focused on measurements at concentration levels corresponding to limit values given in EU Ambient Air Quality Directives and covered reference materials for the reference methods specified in these Directives and for alternative methods based on diffusive sampling. State-of-the-art technologies for the production and certification of the reference materials were identified through literature surveys. Limited batches of reference materials were prepared and, wherever appropriate, tested for homogeneity. The reference materials were subsequently tested in small-scale external verifications, performed by 2-4 laboratories other than the preparation laboratory, aimed at identifying possible discrepancies between concentration values from the preparation processes and experimental values. The results of these verifications revealed possible mechanisms of certification (based on preparation or measurements). The remaining materials were subjected to a one-year stability study.

  19. Glass-based fluorescence reference materials used for optical and biophotonic applications

    NASA Astrophysics Data System (ADS)

    Engel, A.; Ottermann, C.; Resch-Genger, U.; Hoffmann, K.; Schweizer, S.; Selling, J.; Spaeth, J.-M.; Rupertus, V.

    2006-04-01

    Fluorescence techniques are known for their high sensitivity and are widely used as analytical tools and detection methods for product and process control, material sciences, environmental and biotechnical analysis, molecular genetics, cell biology, medical diagnostics, and drug screening. For routine measurements by fluorescence techniques the existence of an improved quality assurance is one of the basic needs. According to DIN/ISO 17025 certified standards are used for fluorescence diagnostics having the drawback of giving relative values only. Typical requirements onto fluorescence reference materials or standards deal with the verification of the instrument performance as well as the improvement of the data comparability. Especially for biomedical applications fluorescence labels are used for the detection of proteins. In particular these labels consist of nano crystalline materials like CdS and CdSe. The field of Non-Cadmium containing materials is under investigation. In order to evaluate whether glass based materials can be used as standards it is necessary to calculate absolute values like absorption/excitation cross sections or relative quantum yields. This can be done using different quantities of dopands in glass, glass ceramics or crystals. The investigated materials are based on different types of glass, silicate, phosphate and boron glass, which play a dominant role for the absorption and emission mechanism. Additional to the so-called elementary fluorescence properties induced by raw earth elements the formation of defects lead to higher cross sections additionally. The main investigations deal with wavelength accuracy and lifetime of doped glasses, glass ceramics and crystalline samples. Moreover intensity patterns, homogeneity aspects and photo stability will be discussed.

  20. City Geology.

    ERIC Educational Resources Information Center

    Markle, Sandra

    1989-01-01

    This article provides information on the evolution of the building material, concrete, and suggests hands-on activities that allow students to experience concrete's qualities, test the heat absorbency of various ground surface materials, discover how an area's geology changes, and search for city fossils. A reproducible activity sheet is included.…

  1. Proposed program for and present status of the Geological Survey's investigation of domestic resources of radioactive raw materials

    USGS Publications Warehouse

    Bulter, A.P.; Killeen, P.L.; Page, G.B.; Rubey, W.W.

    1983-01-01

    This interim report is designed to show the present status of the Geological Survey's information and the parts of a comprehensive program necessary to improve our information about the raw material resources of uranium and thorium. Rarely in geologic work has it been necessary. to determine so completely a nation's resources of useful minerals in so brief a span of time. Ordinarily, information on mineral resources Is accumulated during a long period of years. However, uranium and thorium were suddenly thrust from a position of subsidiary economic interest into one of great strategic importance. Information concerning their occurrence must, therefore, be obtained as rapidly as reliable methods of investigation will permit. Accordingly the program must be at once comprehensive and carried out over an area more extensive than is usual in the search for and appraisal of most other mineral resources.

  2. Determination of arsenic, antimony, bismuth, cadmium, copper, lead, molybdenum, silver and zinc in geological materials by atomic-absorption spectrometry

    USGS Publications Warehouse

    Viets, J.G.; O'Leary, R. M.; Clark, Robert J.

    1984-01-01

    Arsenic, antimony, bismuth, cadmium, copper, lead, molybdenum, silver and zinc are very useful elements in geochemical exploration. In the proposed method, geological samples are fused with potassium pyrosulphate and the fusate is dissolved in a solution of hydrochloric acid, ascorbic acid and potassium iodide. When this solution is shaken with a 10% V/V Aliquat 336 - isobutyl methyl ketone organic phase, the nine elements of interest are selectively partitioned in the organic phase. All nine elements can then be determined in the organic phase using flame atomic-absorption spectrometry. The method is rapid and allows the determination of Ag and Cd at levels down to 0.1 p.p.m., Cu, Mo, and Zn down to 0.5 p.p.m., Pb, Bi and Sb down to 1 p.p.m. and As down to 5 p.p.m. in geological materials.

  3. USGS42 and USGS43: human-hair stable hydrogen and oxygen isotopic reference materials and analytical methods for forensic science and implications for published measurement results.

    PubMed

    Coplen, Tyler B; Qi, Haiping

    2012-01-10

    Because there are no internationally distributed stable hydrogen and oxygen isotopic reference materials of human hair, the U.S. Geological Survey (USGS) has prepared two such materials, USGS42 and USGS43. These reference materials span values commonly encountered in human hair stable isotope analysis and are isotopically homogeneous at sample sizes larger than 0.2 mg. USGS42 and USGS43 human-hair isotopic reference materials are intended for calibration of δ(2)H and δ(18)O measurements of unknown human hair by quantifying (1) drift with time, (2) mass-dependent isotopic fractionation, and (3) isotope-ratio-scale contraction. While they are intended for measurements of the stable isotopes of hydrogen and oxygen, they also are suitable for measurements of the stable isotopes of carbon, nitrogen, and sulfur in human and mammalian hair. Preliminary isotopic compositions of the non-exchangeable fractions of these materials are USGS42(Tibetan hair)δ(2)H(VSMOW-SLAP) = -78.5 ± 2.3‰ (n = 62) and δ(18)O(VSMOW-SLAP) = +8.56 ± 0.10‰ (n = 18) USGS42(Indian hair)δ(2)H(VSMOW-SLAP) = -50.3 ± 2.8‰ (n = 64) and δ(18)O(VSMOW-SLAP) = +14.11 ± 0.10‰ (n = 18). Using recommended analytical protocols presented herein for δ(2)H(VSMOW-SLAP) and δ(18)O(VSMOW-SLAP) measurements, the least squares fit regression of 11 human hair reference materials is δ(2)H(VSMOW-SLAP) = 6.085δ(2)O(VSMOW-SLAP) - 136.0‰ with an R-square value of 0.95. The δ(2)H difference between the calibrated results of human hair in this investigation and a commonly accepted human-hair relationship is a remarkable 34‰. It is critical that readers pay attention to the δ(2)H(VSMOW-SLAP) and δ(18)O(VSMOW-SLAP) of isotopic reference materials in publications, and they need to adjust the δ(2)H(VSMOW-SLAP) and δ(18)O(VSMOW-SLAP) measurement results of human hair in previous publications, as needed, to ensure all results on are on the same scales.

  4. USGS42 and USGS43: Human-hair stable hydrogen and oxygen isotopic reference materials and analytical methods for forensic science and implications for published measurement results

    USGS Publications Warehouse

    Coplen, T.B.; Qi, H.

    2012-01-01

    Because there are no internationally distributed stable hydrogen and oxygen isotopic reference materials of human hair, the U.S. Geological Survey (USGS) has prepared two such materials, USGS42 and USGS43. These reference materials span values commonly encountered in human hair stable isotope analysis and are isotopically homogeneous at sample sizes larger than 0.2 mg. USGS42 and USGS43 human-hair isotopic reference materials are intended for calibration of δ(2)H and δ(18)O measurements of unknown human hair by quantifying (1) drift with time, (2) mass-dependent isotopic fractionation, and (3) isotope-ratio-scale contraction. While they are intended for measurements of the stable isotopes of hydrogen and oxygen, they also are suitable for measurements of the stable isotopes of carbon, nitrogen, and sulfur in human and mammalian hair. Preliminary isotopic compositions of the non-exchangeable fractions of these materials are USGS42(Tibetan hair)δ(2)H(VSMOW-SLAP) = -78.5 ± 2.3‰ (n = 62) and δ(18)O(VSMOW-SLAP) = +8.56 ± 0.10‰ (n = 18) USGS42(Indian hair)δ(2)H(VSMOW-SLAP) = -50.3 ± 2.8‰ (n = 64) and δ(18)O(VSMOW-SLAP) = +14.11 ± 0.10‰ (n = 18). Using recommended analytical protocols presented herein for δ(2)H(VSMOW-SLAP) and δ(18)O(VSMOW-SLAP) measurements, the least squares fit regression of 11 human hair reference materials is δ(2)H(VSMOW-SLAP) = 6.085δ(2)O(VSMOW-SLAP) - 136.0‰ with an R-square value of 0.95. The δ(2)H difference between the calibrated results of human hair in this investigation and a commonly accepted human-hair relationship is a remarkable 34‰. It is critical that readers pay attention to the δ(2)H(VSMOW-SLAP) and δ(18)O(VSMOW-SLAP) of isotopic reference materials in publications, and they need to adjust the δ(2)H(VSMOW-SLAP) and δ(18)O(VSMOW-SLAP) measurement results of human hair in previous publications, as needed, to ensure all results on are on the same scales.

  5. A mussel (Mytilus edulis) tissue certified reference material for the marine biotoxins azaspiracids.

    PubMed

    McCarron, Pearse; Giddings, Sabrina D; Reeves, Kelley L; Hess, Philipp; Quilliam, Michael A

    2015-04-01

    Azaspiracids (AZAs) are lipophilic biotoxins produced by marine algae that can contaminate shellfish and cause human illness. The European Union (EU) regulates the level of AZAs in shellfish destined for the commercial market, with liquid chromatography-mass spectrometry (LC-MS) being used as the official reference method for regulatory analysis. Certified reference materials (CRMs) are essential tools for the development, validation, and quality control of LC-MS methods. This paper describes the work that went into the planning, preparation, characterization, and certification of CRM-AZA-Mus, a tissue matrix CRM, which was prepared as a wet homogenate from mussels (Mytilus edulis) naturally contaminated with AZAs. The homogeneity and stability of CRM-AZA-Mus were evaluated, and the CRM was found to be fit for purpose. Extraction and LC-MS/MS methods were developed to accurately certify the concentrations of AZA1 (1.16 mg/kg), AZA2 (0.27 mg/kg), and AZA3 (0.21 mg/kg) in the CRM. Quantitation methods based on standard addition and matrix-matched calibration were used to compensate for the matrix effects in LC-MS/MS. Other toxins present in this CRM at lower levels were also measured with information values reported for okadaic acid, dinophysistoxin-2, yessotoxin, and several spirolides.

  6. Building a Library Collection on Visual and Physical Disabilities: Basic Materials and Resources. Reference Circular No. 99-01.

    ERIC Educational Resources Information Center

    Library of Congress, Washington, DC. National Library Service for the Blind and Physically Handicapped.

    The materials included in this reference circular are recommended as basic resources for providing current information on general aspects of visual impairments and physical disabilities. The selections, based on the holdings of the Reference Section, National Library Service for the Blind and Physically Handicapped (NLS), were chosen for their…

  7. Reference Material for Radionuclides in Sediment, IAEA-384 (Fangataufa Lagoon Sediment)

    SciTech Connect

    Povinec, P; Pham, M; Barci-Funel, G; Bojanawski, R; Boshkova, T; Burnett, W; Carvalho, F; Chapeyron, B; Cunha, I; Dahlgaard, H; Galabov, N; Gastaud, J; Geering, J; Gomez, I; Green, N; Hamilton, T; Ibanez, F; Majah, M I; John, M; Kanisch, G; Kenna, T; Kloster, M; Korun, M; Wee Kwong, L L; La Rosa, J; Lee, S; Levy-Palomo, I; Malatova, M; Maruo, Y; Mitchell, P; Murciano, I; Nelson, R; Oh, J; Oregioni, B; Petit, G L; Pettersson, H; Reineking, A; Smedley, P; Suckow, A; der Struijs, T v; Voors, P; Yoshimizu, K; Wyse, E

    2005-09-23

    The IAEA Marine Environment Laboratory (IAEA-MEL) in Monaco has conducted intercomparison exercises on radionuclides in marine samples for many years as part of its contribution to the IAEA's program of Analytical Quality Control Services (AQCS). An important part of the AQCS program has been a production of Reference Materials (RMs) and their provision to radioanalytical laboratories. The RMs have been developed for different marine matrices (sediment, water, biota), with accuracy and precision required for the present state of the art of radiometrics and mass spectrometry methods. The RMs have been produced as the final products of world-wide intercomparison exercises organized during last 30 years. A total of 44 intercomparison exercises were undertaken and 39 RMs were produced for radionuclides in the marine environment. All required matrices (seawater, biota, sediment) have been covered with radionuclide concentrations ranging from typical environmental levels to elevated levels affected by discharges from nuclear reprocessing plants. The long-term availability of RMs (over 10 years) requires the use of very specific techniques to collect and pretreat large quantities of material (e.g., in excess of 100 kg) in order to ensure sample stability and homogenization of any analytes of interest. The production of a RM is therefore a long process, covering the identification of needs, sample collection, pre-treatment, homogenization, bottling, distribution to laboratories, evaluation of data, preliminary reporting, additional analyses in expert laboratories, certification of the material, and finally issuing the RM. In this paper we describe a reference material IAEA-384, Fangataufa lagoon sediment, designed for determination of anthropogenic and natural radionuclides in the marine environment. This RM has been prepared with the aim of testing the performance of analytical laboratories to measure the activity of these radionuclides in a sediment sample contaminated

  8. Acoustic mapping of the regional seafloor geology in and around Hawaiian ocean dredged-material disposal sites

    USGS Publications Warehouse

    Torresan, Michael E.; Gardner, James V.

    2000-01-01

    During January and February 1998 the U.S. Geological Survey Coastal and Marine Geology Team (USGS) conducted regional high-resolution multibeam mapping surveys of the area surrounding EPA-designated ocean disposal sites located offshore of the Hawaiian Islands of Oahu, Kauai, Maui, and Hawaii. The sites are all located within 5 nautical miles of shore on insular shelves or slopes. Regional maps were required of areas much larger than the disposal sites themselves to assess both the regional seafloor geology and the immediate vicinity of the disposal sites. The purpose of the disposal site surveys was to delimit the extent of disposal material by producing detailed bathymetric and backscatter maps of the seafloor with a ± 1 m spatial accuracy and <1% depth error. The advantage of using multibeam over conventional towed, single-beam sidescan sonar is that the multibeam data are accurately georeferenced for precise location of all imaged features. The multibeam produces a coregistered acoustic-backscatter map that is often required to locate individual disposal deposits. These data were collected by the USGS as part of its regional seafloor mapping and in support of ocean disposal site monitoring studies conducted in cooperation with the US Environmental Protection Agency (EPA) and the US Army Corps of Engineers (COE).

  9. Soot reference materials for instrument calibration and intercomparisons: a workshop summary with recommendations

    NASA Astrophysics Data System (ADS)

    Baumgardner, D.; Popovicheva, O.; Allan, J.; Bernardoni, V.; Cao, J.; Cavalli, F.; Cozic, J.; Diapouli, E.; Eleftheriadis, K.; Genberg, P. J.; Gonzalez, C.; Gysel, M.; John, A.; Kirchstetter, T. W.; Kuhlbusch, T. A. J.; Laborde, M.; Lack, D.; Müller, T.; Niessner, R.; Petzold, A.; Piazzalunga, A.; Putaud, J. P.; Schwarz, J.; Sheridan, P.; Subramanian, R.; Swietlicki, E.; Valli, G.; Vecchi, R.; Viana, M.

    2012-08-01

    Soot, which is produced from biomass burning and the incomplete combustion of fossil and biomass fuels, has been linked to regional and global climate change and to negative health problems. Scientists measure the properties of soot using a variety of methods in order to quantify source emissions and understand its atmospheric chemistry, reactivity under emission conditions, interaction with solar radiation, influence on clouds, and health impacts. A major obstacle currently limiting progress is the absence of established standards or reference materials for calibrating the many instruments used to measure the various properties of soot. The current state of availability and practicability of soot standard reference materials (SRMs) was reviewed by a group of 50 international experts during a workshop in June of 2011. The workshop was convened to summarize the current knowledge on soot measurement techniques, identify the measurement uncertainties and limitations related to the lack of soot SRMs, and identify attributes of SRMs that, if developed, would reduce measurement uncertainties. The workshop established that suitable SRMs are available for calibrating some, but not all, measurement methods. The community of users of the single-particle soot-photometer (SP2), an instrument using laser-induced incandescence, identified a suitable SRM, fullerene soot, but users of instruments that measure light absorption by soot collected on filters did not. Similarly, those who use thermal optical analysis (TOA) to analyze the organic and elemental carbon components of soot were not satisfied with current SRMs. The workshop, and subsequent, interactive discussions, produced a number of recommendations for the development of new SRMs, and their implementation, that would be suitable for the different soot measurement methods.

  10. T-2 and HT-2 toxins in oat flakes: development of a certified reference material.

    PubMed

    Köppen, Robert; Bremser, Wolfram; Stephan, Ina; Klein-Hartwig, Karin; Rasenko, Tatjana; Koch, Matthias

    2015-04-01

    Trichothecene mycotoxins, with T-2 and HT-2 toxins being the main representatives of the type A subgroup, are naturally and worldwide occurring contaminants frequently found in grain-based food and feed. Due to the high consumption of these products and the potential health risk associated herewith, concerns about the safety and quality of food and feed have increased over the last decades at both governmental and consumer levels. Since it is not possible to avoid their occurrence, tremendous efforts have been performed to identify and monitor mycotoxins in food and feed to make their consumption safe. However, suitable certified reference materials (CRMs) intended for quality assurance and quality control purposes are still lacking for many mycotoxin-matrix combinations. Therefore, in the framework of a European Reference Material (ERM®) project, the first CRM for T-2 and HT-2 toxin in ground oat flakes (ERM®-BC720) was developed according to the requirements of ISO Guide 35. The whole process of ERM®-BC720 development, including sample preparation, homogeneity and stability studies and value assignment, is presented. The assignment of the certified mass fractions was based upon an in-house study using high-performance liquid chromatography isotope-dilution tandem mass spectrometry. Simultaneously, an interlaboratory comparison study involving 24 expert laboratories was conducted in order to support the in-house certification study. The certified values and their corresponding expanded uncertainties (k = 2) for both T-2 and HT-2 toxin in ERM®-BC720, traceable to the international system of units, are (82 ± 4) μg kg(-1) and (81 ± 4) μg kg(-1), respectively.

  11. Palm-Based Standard Reference Materials for Iodine Value and Slip Melting Point

    PubMed Central

    Tarmizi, Azmil Haizam Ahmad; Lin, Siew Wai; Kuntom, Ainie

    2008-01-01

    This work described study protocols on the production of Palm-Based Standard Reference Materials for iodine value and slip melting point. Thirty-three laboratories collaborated in the inter-laboratory proficiency tests for characterization of iodine value, while thirty-two laboratories for characterization of slip melting point. The iodine value and slip melting point of palm oil, palm olein and palm stearin were determined in accordance to MPOB Test Methods p3.2:2004 and p4.2:2004, respectively. The consensus values and their uncertainties were based on the acceptability of statistical agreement of results obtained from collaborating laboratories. The consensus values and uncertainties for iodine values were 52.63 ± 0.14 Wijs in palm oil, 56.77 ± 0.12 Wijs in palm olein and 33.76 ± 0.18 Wijs in palm stearin. For the slip melting points, the consensus values and uncertainties were 35.6 ± 0.3 °C in palm oil, 22.7 ± 0.4 °C in palm olein and 53.4 ± 0.2 °C in palm stearin. Repeatability and reproducibility relative standard deviations were found to be good and acceptable, with values much lower than that of 10%. Stability of Palm-Based Standard Reference Materials remained stable at temperatures of −20 °C, 0 °C, 6 °C and 24 °C upon storage for one year. PMID:19609396

  12. T-2 and HT-2 toxins in oat flakes: development of a certified reference material.

    PubMed

    Köppen, Robert; Bremser, Wolfram; Stephan, Ina; Klein-Hartwig, Karin; Rasenko, Tatjana; Koch, Matthias

    2015-04-01

    Trichothecene mycotoxins, with T-2 and HT-2 toxins being the main representatives of the type A subgroup, are naturally and worldwide occurring contaminants frequently found in grain-based food and feed. Due to the high consumption of these products and the potential health risk associated herewith, concerns about the safety and quality of food and feed have increased over the last decades at both governmental and consumer levels. Since it is not possible to avoid their occurrence, tremendous efforts have been performed to identify and monitor mycotoxins in food and feed to make their consumption safe. However, suitable certified reference materials (CRMs) intended for quality assurance and quality control purposes are still lacking for many mycotoxin-matrix combinations. Therefore, in the framework of a European Reference Material (ERM®) project, the first CRM for T-2 and HT-2 toxin in ground oat flakes (ERM®-BC720) was developed according to the requirements of ISO Guide 35. The whole process of ERM®-BC720 development, including sample preparation, homogeneity and stability studies and value assignment, is presented. The assignment of the certified mass fractions was based upon an in-house study using high-performance liquid chromatography isotope-dilution tandem mass spectrometry. Simultaneously, an interlaboratory comparison study involving 24 expert laboratories was conducted in order to support the in-house certification study. The certified values and their corresponding expanded uncertainties (k = 2) for both T-2 and HT-2 toxin in ERM®-BC720, traceable to the international system of units, are (82 ± 4) μg kg(-1) and (81 ± 4) μg kg(-1), respectively. PMID:25399074

  13. Characterization of Perchlorate in a New Frozen Human Urine Standard Reference Material

    PubMed Central

    Yu, Lee L.; Jarrett, Jeffery M.; Davis, W. Clay; Kilpatrick, Eric L.; Oflaz, Rabia; Turk, Gregory C.; Leber, Dennis D.; Valentin, Liza; Morel-Espinosa, Maria; Blount, Benjamin C.

    2015-01-01

    Perchlorate, an inorganic anion, has recently been recognized as an environmental contaminant by the U.S. Environmental Protection Agency (EPA). Urine is the preferred matrix for assessment of human exposure to perchlorate. Although the measurement technique for perchlorate in urine was developed in 2005, the calibration and quality assurance aspects of the metrology infrastructure for perchlorate are still lacking in that there is no certified reference material (CRM) traceable to the International System of Units (SI). To meet the quality assurance needs in biomonitoring measurements of perchlorate and the related anions that affect thyroid health, the National Institute of Standards and Technology (NIST) in collaboration with the Centers for Disease Control and Prevention (CDC) developed Standard Reference Material (SRM) 3668 Mercury, Perchlorate, and Iodide in Frozen Human Urine. SRM 3668 consists of perchlorate, nitrate, thiocyanate, iodine, and mercury in urine at two levels that represent the 50th and 95th percentiles, respectively, of the concentrations (with some adjustments) in the U.S. population. It is the first CRM being certified for perchlorate. Measurements leading to the certification of perchlorate were made collaboratively at NIST and CDC using three methods based on liquid or ion chromatography tandem mass spectrometry (LC-MS/MS or IC-MS/MS). Potential sources of bias were analyzed and results were compared for the three methods. Perchlorate in SRM 3668 Level I urine was certified to be 2.70 μg L−1 ± 0.21 μg L−1, and for SRM 3668 Level II urine, the certified value is 13.47 μg L−1 ± 0.96 μg L−1. PMID:22850897

  14. Feasibility study on production of a matrix reference material for cyanobacterial toxins.

    PubMed

    Hollingdale, Christie; Thomas, Krista; Lewis, Nancy; Békri, Khalida; McCarron, Pearse; Quilliam, Michael A

    2015-07-01

    The worldwide increase in cyanobacterial contamination of freshwater lakes and rivers is of great concern as many cyanobacteria produce potent hepatotoxins and neurotoxins (cyanotoxins). Such toxins pose a threat to aquatic ecosystems, livestock, and drinking water supplies. In addition, dietary supplements prepared from cyanobacteria can pose a risk to consumers if they contain toxins. Analytical monitoring for toxins in the environment and in consumer products is essential for the protection of public health. Reference materials (RMs) are an essential tool for the development and validation of analytical methods and are necessary for ongoing quality control of monitoring operations. Since the availability of appropriate RMs for cyanotoxins has been very limited, the present study was undertaken to examine the feasibility of producing a cyanobacterial matrix RM containing various cyanotoxins. The first step was large-scale culturing of various cyanobacterial cultures that produce anatoxins, microcystins, and cylindrospermopsins. After harvesting, the biomass was lyophilized, blended, homogenized, milled, and bottled. The moisture content and physical characteristics were assessed in order to evaluate the effectiveness of the production process. Toxin levels were measured by liquid chromatography with tandem mass spectrometry and ultraviolet detection. The reference material was found to be homogeneous for toxin content. Stability studies showed no significant degradation of target toxins over a period of 310 days at temperatures up to +40 °C except for the anatoxin-a, which showed some degradation at +40 °C. These results show that a fit-for-purpose matrix RM for cyanotoxins can be prepared using the processes and techniques applied in this work.

  15. Advances in Huntington's disease diagnostics: development of a standard reference material.

    PubMed

    Levin, Barbara C; Richie, Kristy L; Jakupciak, John P

    2006-07-01

    Huntington's disease (HD) is a neurodegenerative disease that affects four to seven individuals per 100,000. The onset of symptoms usually begins in middle age, although approximately 5% become symptomatic as juveniles. Death occurs approximately 15 years following the onset of symptoms, which include choreic movements, cognitive decline and psychiatric changes. HD is an autosomal dominant inherited disease that is associated with an expansion of a trinucleotide (CAG) repeat located on chromosome 4. Physicians rely on a positive family history, and diagnostic and genetic tests to detect the expansion in the number of CAG trinucleotide repeats in the HD gene to confirm the diagnosis. More than 99% of HD patients have 40 or more CAG triplet repeats and, therefore, targeted mutational analysis is greater than 99% sensitive. Individuals with 26 triplet repeats or less are normal, and while those with 27-35 repeats may not demonstrate symptoms themselves, their offspring may have the disease. Individuals with 36-39 repeats may or may not exhibit symptoms. The College of American Pathology/American College of Medical Genetics Biochemical and Molecular Genetics Resource Committee has emphasized the need to standardize the methodology for the determination of the accurate number of CAG repeats. This will prevent false-positive or -negative results when conducting predictive or prenatal testing of at-risk individuals. The National Institute of Standards and Technology is developing a standard reference material to provide these positive and negative controls needed by clinical testing laboratories. The use of a HD standard reference material will provide the quality control and assurance that data from different laboratories are both comparable and accurate.

  16. Preparation of waterproof OSL dosimeters from hygroscopic materials with a special reference to NaCl:Cu

    NASA Astrophysics Data System (ADS)

    More, Y. K.; Wankhede, S. P.; Patil, R. R.; Kulkarni, M. S.; Kumar, Munish; Moharil, S. V.

    2016-05-01

    Optically stimulated luminescence (OSL) originally developed for geological/archaeological dating, has been found very useful for diverse applications in the field of radiation dosimetry. There is still a scarcity of OSL materials with demonstrated properties suited to dosimetry applications. Progress on the development of OSL materials with engineered properties has been slow and most research has focused on the OSL characterization of existing materials. One of the reasons for availability of only a handful of OSL dosimetry materials with adequate properties is that they have to satisfy certain stringent conditions necessary for such applications. Especially, hygroscopic materials are considered totally unsuitable. The efforts were made in our laboratory to overcome this problem. It is shown here that "water-proof" dosimeters can be prepared from even hygroscopic materials such as NaCl.

  17. Using Remote Sensing Techniques to Assess the Geologic Context of Olivine-Bearing Materials within Terra Sirenum, Mars

    NASA Astrophysics Data System (ADS)

    Anderson, M.; Osterloo, M. M.

    2015-12-01

    Understanding olivine-bearing materials in Terra Sirenum provides insight into the magmatic and hydrologic processes that shaped the Southern Highlands of Mars. Our study addresses two questions: "What is the geologic context of olivine compositions in the study area?" and "What does olivine abundance, composition, and geologic context suggest about the magmatic and weathering processes in our study area?" To answer these questions, we mapped olivine deposits within a region of Terra Sirenum using JMARS [1]. We used Thermal Emission Imaging System (THEMIS) data to map the extent of olivine deposits and to understand their degree of consolidation. To investigate olivine composition, we used the Thermal Emission Spectrometer (TES) global maps of Forsterite/Fayalite compositions [2]. We found that the olivine compositions vary from most iron-rich types (Fo01) to the most magnesium-rich (Fo91), with the vast majority identified as Fo68. The results of our study are consistent with those implied by the magma overturn model [3], which explains the compositional changes in Martian magmas over time. In addition, the extent of olivine-bearing deposits within our study area suggests that mechanical weathering (e.g., aeolian and gravity-driven processes) is more likely to dominate the sedimentary record in recent geologic time over water-driven processes. We will present our results, which detail the present-day surface geology of our study area in Terra Sirenum. Our results have implications for Martian magma evolution as well as the extent water has played in shaping the surface of the planet. [1] Gorelick, N., et al. (2003), Lunar and Planetary Science, XXXIV. [2] Koeppen, W.C., et al. (2008), Journal of Geophysical Research, 113, E002984. [3] Elkins-Tanton, L.T., et al. (2003), Meteorites & Planetary Science, 38, tb00013.

  18. Milk and serum standard reference materials for monitoring organic contaminants in human samples.

    PubMed

    Schantz, Michele M; Eppe, Gauthier; Focant, Jean-François; Hamilton, Coreen; Heckert, N Alan; Heltsley, Rebecca M; Hoover, Dale; Keller, Jennifer M; Leigh, Stefan D; Patterson, Donald G; Pintar, Adam L; Sharpless, Katherine E; Sjödin, Andreas; Turner, Wayman E; Vander Pol, Stacy S; Wise, Stephen A

    2013-02-01

    Four new Standard Reference Materials (SRMs) have been developed to assist in the quality assurance of chemical contaminant measurements required for human biomonitoring studies, SRM 1953 Organic Contaminants in Non-Fortified Human Milk, SRM 1954 Organic Contaminants in Fortified Human Milk, SRM 1957 Organic Contaminants in Non-Fortified Human Serum, and SRM 1958 Organic Contaminants in Fortified Human Serum. These materials were developed as part of a collaboration between the National Institute of Standards and Technology (NIST) and the Centers for Disease Control and Prevention (CDC) with both agencies contributing data used in the certification of mass fraction values for a wide range of organic contaminants including polychlorinated biphenyl (PCB) congeners, chlorinated pesticides, polybrominated diphenyl ether (PBDE) congeners, and polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners. The certified mass fractions of the organic contaminants in unfortified samples, SRM 1953 and SRM 1957, ranged from 12 ng/kg to 2200 ng/kg with the exception of 4,4'-DDE in SRM 1953 at 7400 ng/kg with expanded uncertainties generally <14 %. This agreement suggests that there were no significant biases existing among the multiple methods used for analysis. PMID:23132544

  19. Milk and serum standard reference materials for monitoring organic contaminants in human samples.

    PubMed

    Schantz, Michele M; Eppe, Gauthier; Focant, Jean-François; Hamilton, Coreen; Heckert, N Alan; Heltsley, Rebecca M; Hoover, Dale; Keller, Jennifer M; Leigh, Stefan D; Patterson, Donald G; Pintar, Adam L; Sharpless, Katherine E; Sjödin, Andreas; Turner, Wayman E; Vander Pol, Stacy S; Wise, Stephen A

    2013-02-01

    Four new Standard Reference Materials (SRMs) have been developed to assist in the quality assurance of chemical contaminant measurements required for human biomonitoring studies, SRM 1953 Organic Contaminants in Non-Fortified Human Milk, SRM 1954 Organic Contaminants in Fortified Human Milk, SRM 1957 Organic Contaminants in Non-Fortified Human Serum, and SRM 1958 Organic Contaminants in Fortified Human Serum. These materials were developed as part of a collaboration between the National Institute of Standards and Technology (NIST) and the Centers for Disease Control and Prevention (CDC) with both agencies contributing data used in the certification of mass fraction values for a wide range of organic contaminants including polychlorinated biphenyl (PCB) congeners, chlorinated pesticides, polybrominated diphenyl ether (PBDE) congeners, and polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners. The certified mass fractions of the organic contaminants in unfortified samples, SRM 1953 and SRM 1957, ranged from 12 ng/kg to 2200 ng/kg with the exception of 4,4'-DDE in SRM 1953 at 7400 ng/kg with expanded uncertainties generally <14 %. This agreement suggests that there were no significant biases existing among the multiple methods used for analysis.

  20. Preparation and application of a fortified hair reference material for the determination of methamphetamine and amphetamine.

    PubMed

    Lee, Sooyeun; Park, Yonghoon; Han, Eunyoung; Choe, Sanggil; Lim, Miae; Chung, Heesun

    2008-07-01

    Quality assurance is one of the major issues in forensic analytical laboratories, where the need for a reference material (RM) has rapidly increased. RMs are very useful for method development and validation, internal quality control or proficiency tests. In the present study, we prepared a RM using drug-free hair for the determination of methamphetamine (MA) and its main metabolite, amphetamine (AP) according to the recommendations of ISO Guide 35. The concentrations of MA and AP were determined using two extraction methods, agitation with 1% HCl in methanol at 38 degrees C and ultrasonication with methanol/5M HCl (20:1), followed by gas chromatography/mass spectrometry (GC/MS) after derivatization with trifluoroacetic anhydride (TFAA). The assignment of values was conducted through the homogeneity study and characterization of the material. Furthermore, an internal proficiency test was performed with the prepared RM, of which the results were compared with those of the authentic hair RM prepared in our previous study. As a result, a hair RM containing MA and AP was prepared at the level of 4.86+/-0.69 ng/mg and 4.63+/-0.44 ng/mg, respectively. Most participants showed satisfactory performances in the internal proficiency test with the both RMs. The hair RM prepared in this study demonstrated its suitability for quality assurance in forensic laboratories.

  1. Development of a candidate certified reference material of cypermethrin in green tea.

    PubMed

    Sin, Della W M; Chan, Pui-kwan; Cheung, Samuel T C; Wong, Yee-Lok; Wong, Siu-kay; Mok, Chuen-shing; Wong, Yiu-chung

    2012-04-01

    This paper presents the preparation of a candidate certified reference material (CRM) of cypermethrin in green tea, GLHK-11-01a according to the requirements of ISO Guide 34 and 35. Certification of the material was performed using a newly developed isotope dilution mass spectrometry (IDMS) approach, with gas chromatography high resolution mass spectrometry (GC-HRMS) and gas chromatography-tandem mass spectrometry (GC-MS/MS). Statistical analysis (one-way ANOVA) showed excellent agreement of the analytical data sets generated from the two mass spectrometric detections. The characterization methods have also been satisfactorily applied in an Asia-Pacific Metrology Program (APMP) interlaboratory comparison study. Both the GC-HRIDMS and GC-IDMS/MS methods proved to be sufficiently reliable and accurate for certification purpose. The certified value of cypermethrin in dry mass fraction was 148 μg kg(-1) and the associated expanded uncertainty was 14μg kg(-1). The uncertainty budget was evaluated from sample in homogeneity, long-term and short-term stability and variability in the characterization procedure. GLHK-11-01a is primarily developed to support the local and wider testing community on need basis in quality assurance work and in seeking accreditation. PMID:22405308

  2. Development of the NIST bone ash standard reference material for environmental radioactivity measurement.

    PubMed

    Lin, Z; Inn, K G; Altzitzoglou, T; Arnold, D; Cavadore, D; Ham, G J; Korun, M; Wershofen, H; Takata, Y; Young, A

    1998-01-01

    The bone ash standard reference material (SRM), a blend of 4% contaminated human bone and 96% diluent bovine bone, has been developed for radiochemical method validation and quality control for radio-bone analysis. The massic activities of 90Sr, 226Ra, 230Th, 232Th, 234U, 235U, 238U, 238Pu, (239 + 240)Pu and (243 + 244)Cm were certified using a variety of radiochemical procedures and detection methods. Measurements confirmed undetectable radionuclide heterogeneity down to a sample size of 5 g. thereby implying adequate blending of particulate materials with dilution factors of up to 17,900. The results among most of the intercomparison laboratories and their methods were consistent. Disequilibrium was observed for decay chains: 234U(0.67 mBq/g)-230Th(0.47 mBq/g)-226Ra(15.1 mBq/g)-210Pb(23 mBq/g)-210Po(13 mBq/g) and 232Th(0.99 mBq/g)-228 Ra(6.1 mBq/g)-228Th(7.1 mBq/g). The disequilibria were the results of mixing occupationally contaminated human bone with natural bovine bone and the fractionation during internal biological processes. The massic activity of 210Pb, 228Th and 241Am were not certified because of insufficient 228Ra and 241Pu data and lack of knowledge in how 222Rn and its daughters will be fractionated in the SRM bottle over time.

  3. Certification of a reference material of metal content in atmospheric particles deposited on filters.

    PubMed

    Oster, Caroline; Labarraque, Guillaume; Fisicaro, Paola

    2015-04-01

    Air quality is one of the areas in Europe where a series of EU Directives have been published with the aim of achieving improved long-term and harmonised air quality objectives across the European Union. This paper describes the production of a certified reference material, aiming to support QA/QC programmes of analytical laboratories in the framework of the air quality monitoring activities. The certified values are the As, Cd, Ni and Pb masses in PM10 particles deposited on quartz filters (CRM SL-MR-2-PSF-01). All the steps of the certification, i.e. the material characterisation, homogeneity and stability evaluation and uncertainty calculation, were performed according to the ISO guide 35 guidelines. The certification was conducted using the characterisation by a single method approach based on isotope dilution for cadmium, nickel, and lead and gravimetric standard addition calibration for arsenic associated with inductively coupled mass spectrometry (ICP-MS). The amounts of the four elements are in the range of the target values regulated by EU Directives.

  4. Geologic Mapping and Paired Geochemical-Paleomagnetic Sampling of Reference Sections in the Grande Ronde Basalt: An Example from the Bingen Section, Columbia River Gorge, Washington

    NASA Astrophysics Data System (ADS)

    Sawlan, M.; Hagstrum, J. T.; Wells, R. E.

    2011-12-01

    We have completed comprehensive geochemical (GC) and paleomagnetic (PM) sampling of individual lava flows from eight reference stratigraphic sections in the Grande Ronde Basalt (GRB), Columbia River Basalt Group [Hagstrum et al., 2009, GSA Ann. Mtg, Portland (abst); Hagstrum et al., 2010, AGU Fall Mtg, San Francisco (abst)]. These sections, distributed across the Columbia Plateau and eastern Columbia River Gorge, contain as many as 30 flows, are up to 670 m thick, span upper magneto-stratigraphic zones R2 and N2, and, in some locations, also contain one or more N1 flows. In concert with GC and PM sampling, we have carried out detailed geologic mapping of these sections, typically at a scale of 1:3,000 to 1:5,000, using GPS, digital imagery from the National Aerial Imagery Program (NAIP), and compilation in GIS. GRB member and informal unit names of Reidel et al. [1989, GSA Sp. Paper 239] generally have been adopted, although two new units are identified and named within the N2 zone. Notably, a distinctive PM direction for intercalated lavas of several lower N2 units indicates coeval eruption of compositionally distinct units; this result contrasts with the scenario of serial stratigraphic succession of GRB units proposed by Reidel et al. [1989]. Our objectives in the mapping include: Confirming the integrity of the stratigraphic sequences by documenting flow contacts and intraflow horizons (changes in joint patterns or vesicularity); assessing fault displacements; and, establishing precisely located samples in geologic context such that selected sites can be unambiguously reoccupied. A geologic map and GC-PM data for the Bingen section, along the north side of the Columbia River, are presented as an example of our GRB reference section mapping and sampling. One of our thicker sections (670 m) along which 30 flows are mapped, the Bingen section spans 7 km along WA State Hwy 14, from near the Hood River Bridge ESE to Locke Lake. This section cuts obliquely through a

  5. Distribution and geological sources of selenium in environmental materials in Taoyuan County, Hunan Province, China.

    PubMed

    Ni, Runxiang; Luo, Kunli; Tian, Xinglei; Yan, Songgui; Zhong, Jitai; Liu, Maoqiu

    2016-06-01

    The selenium (Se) distribution and geological sources in Taoyuan County, China, were determined by using hydride generation atomic fluorescence spectrometry on rock, soil, and food crop samples collected from various geological regions within the county. The results show Se contents of 0.02-223.85, 0.18-7.05, and 0.006-5.374 mg/kg in the rock, soil, and food crops in Taoyuan County, respectively. The region showing the highest Se content is western Taoyuan County amid the Lower Cambrian and Ediacaran black rock series outcrop, which has banding distributed west to east. A relatively high-Se environment is found in the central and southern areas of Taoyuan County, where Quaternary Limnetic sedimentary facies and Neoproterozoic metamorphic volcanic rocks outcrop, respectively. A relatively low-Se environment includes the central and northern areas of Taoyuan County, where Middle and Upper Cambrian and Ordovician carbonate rocks and Cretaceous sandstones and conglomerates outcrop. These results indicate that Se distribution in Taoyuan County varies markedly and is controlled by the Se content of the bedrock. The Se-enriched Lower Cambrian and Ediacaran black rock series is the primary source of the seleniferous environment observed in Taoyuan County. Potential seleniferous environments are likely to be found near outcrops of the Lower Cambrian and Ediacaran black rock series in southern China.

  6. Distribution and geological sources of selenium in environmental materials in Taoyuan County, Hunan Province, China.

    PubMed

    Ni, Runxiang; Luo, Kunli; Tian, Xinglei; Yan, Songgui; Zhong, Jitai; Liu, Maoqiu

    2016-06-01

    The selenium (Se) distribution and geological sources in Taoyuan County, China, were determined by using hydride generation atomic fluorescence spectrometry on rock, soil, and food crop samples collected from various geological regions within the county. The results show Se contents of 0.02-223.85, 0.18-7.05, and 0.006-5.374 mg/kg in the rock, soil, and food crops in Taoyuan County, respectively. The region showing the highest Se content is western Taoyuan County amid the Lower Cambrian and Ediacaran black rock series outcrop, which has banding distributed west to east. A relatively high-Se environment is found in the central and southern areas of Taoyuan County, where Quaternary Limnetic sedimentary facies and Neoproterozoic metamorphic volcanic rocks outcrop, respectively. A relatively low-Se environment includes the central and northern areas of Taoyuan County, where Middle and Upper Cambrian and Ordovician carbonate rocks and Cretaceous sandstones and conglomerates outcrop. These results indicate that Se distribution in Taoyuan County varies markedly and is controlled by the Se content of the bedrock. The Se-enriched Lower Cambrian and Ediacaran black rock series is the primary source of the seleniferous environment observed in Taoyuan County. Potential seleniferous environments are likely to be found near outcrops of the Lower Cambrian and Ediacaran black rock series in southern China. PMID:26563208

  7. Testing for fullerenes in geologic materials: Oklo carbonaceous substances, Karelian shungites, Sudbury Black Tuff

    NASA Astrophysics Data System (ADS)

    Mossman, David; Eigendorf, Guenter; Tokaryk, Dennis; Gauthier-Lafaye, François; Guckert, Kristal D.; Melezhik, Victor; Farrow, Catharine E. G.

    2003-03-01

    Fullerenes have been reported from diverse geologic environments since their discovery in shungite from Karelian Russia. Our investigation is prompted by the presence of onionskin-like structures in some carbonaceous substances associated with the fossil nuclear fission reactors of Oklo, Gabon. The same series of extractions and the same instrumental techniques, laser desorption ionization and high-resolution mass spectroscopy (electron-impact mass spectroscopy), were employed to test for fullerenes in samples from three different localities: two sites containing putative fullerenes (Sudbury Basin and Russian Karelia) and one new location (Oklo, Gabon). We confirm the presence of fullerenes (C60 and C70) in the Black Tuff of the Onaping Formation impact breccia in the Sudbury Basin, but we find no evidence of fullerenes in shungite samples from various locations in Russian Karelia. Analysis of carbonaceous substances associated with the natural nuclear fission reactors of Oklo yields no definitive signals for fullerenes. If fullerenes were produced during sustained nuclear fission at Oklo, then they are present below the detection limit (˜100 fmol), or they have destabilized since formation. Contrary to some expectations, geologic occurrences of fullerenes are not commonplace.

  8. Simulations of Fracture and Fragmentation of Geologic Materials using Combined FEM/DEM Analysis

    SciTech Connect

    Morris, J P; Rubin, M B; Block, G I; Bonner, M P

    2005-05-26

    Results are presented from a study investigating the effect of explosive and impact loading on geological media using the Livermore Distinct Element Code (LDEC). LDEC was initially developed to simulate tunnels and other structures in jointed rock masses with large numbers of intact polyhedral blocks. However, underground structures in jointed rock subjected to explosive loading can fail due to both rock motion along preexisting interfaces and fracture of the intact rock mass itself. Many geophysical applications, such as projectile penetration into rock, concrete targets, and boulder fields, require a combination of continuum and discrete methods in order to predict the formation and interaction of the fragments produced. In an effort to model these types of problems, we have implemented Cosserat point theory and cohesive element formulations into the current version of LDEC, thereby allowing for dynamic fracture and combined finite element/discrete element simulations. Results of a large-scale LLNL simulation of an explosive shock wave impacting an elaborate underground facility are also discussed. It is confirmed that persistent joints lead to an underestimation of the impact energy needed to fill the tunnel systems with rubble. Non-persistent joint patterns, which are typical of real geologies, inhibit shear within the surrounding rock mass and significantly increase the load required to collapse a tunnel.

  9. Developing qualitative LC-MS methods for characterization of Vaccinium berry Standard Reference Materials.

    PubMed

    Lowenthal, Mark S; Phillips, Melissa M; Rimmer, Catherine A; Rudnick, Paul A; Simón-Manso, Yamil; Stein, Stephen E; Tchekhovskoi, Dmitrii; Phinney, Karen W

    2013-05-01

    Standard Reference Materials (SRMs) offer the scientific community a stable and homogenous source of material that holds countless application possibilities. Traditionally, the National Institute of Standards and Technology (NIST) has provided SRMs with associated quantitative information (certified values) for a select group of targeted analytes as measured in a solution or complex matrix. While the current needs of the SRM community are expanding to include non-quantitative data, NIST is attempting to broaden the scope of how and what information is offered to the SRM community by providing qualitative information about biomaterials, such as chromatographic fingerprints and profiles of untargeted identifications. In this work, metabolomic and proteomic profiling efforts were employed to characterize a suite of six Vaccinium berry SRMs. In the discovery phase, liquid chromatography-tandem mass spectrometry (LC-MS/MS) data was matched to mass spectral libraries; a subsequent validation phase based on multiple-reaction monitoring LC-MS/MS relied on both retention time matching of authentic standards along with fragmentation data for a qualitative overview of the most prominent organic compounds present. Definitive and putative identifications were determined for over 70 metabolites based on reporting guidelines set forth by the Metabolomics Standards Initiative (Metabolomics 3(3):211-221, 2007), and the capability of electrospray ionization mass spectrometry (ESI-MS) to profile untargeted metabolites within a complex matrix using mass spectral matching is demonstrated. Bottom-up proteomic analyses were possible using peptide databases translated from expressed sequence tags (ESTs). Homology searches provided identification of novel Vaccinium proteins based on homology to related genera. Chromatographic fingerprints of these berry materials were acquired for supplemental qualitative information to be provided to users of these SRMs. An unbounded set of qualitative

  10. Introduction to selected references on fossil fuels of the central and southern Appalachian basin: Chapter H.1 in Coal and petroleum resources in the Appalachian basin: distribution, geologic framework, and geochemical character

    USGS Publications Warehouse

    Ruppert, Leslie F.; Lentz, Erika E.; Tewalt, Susan J.; Román Colón, Yomayra A.; Ruppert, Leslie F.; Ryder, Robert T.

    2014-01-01

    The Appalachian basin contains abundant coal and petroleum resources that have been studied and extracted for at least 150 years. In this volume, U.S. Geological Survey (USGS) scientists describe the geologic framework and geochemical character of the fossil-fuel resources of the central and southern Appalachian basin. Separate subchapters (some previously published) contain geologic cross sections; seismic profiles; burial history models; assessments of Carboniferous coalbed methane and Devonian shale gas; distribution information for oil, gas, and coal fields; data on the geochemistry of natural gas and oil; and the fossil-fuel production history of the basin. Although each chapter and subchapter includes references cited, many historical or other important references on Appalachian basin and global fossil-fuel science were omitted because they were not directly applicable to the chapters.

  11. Determination of indium in geological materials by electrothermal-atomization atomic absorption spectrometry with a tungsten-impregnated graphite furance

    USGS Publications Warehouse

    Zhou, L.; Chao, T.T.; Meier, A.L.

    1984-01-01

    The sample is fused with lithium metaborate and the melt is dissolved in 15% (v/v) hydrobromic acid. Iron(III) is reduced with ascorbic acid to avoid its coextraction with indium as the bromide into methyl isobutyl ketone. Impregnation of the graphite furnace with sodium tungstate, and the presence of lithium metaborate and ascorbic acid in the reaction medium improve the sensitivity and precision. The limits of determination are 0.025-16 mg kg-1 indium in the sample. For 22 geological reference samples containing more than 0.1 mg kg-1 indium, relative standard deviations ranged from 3.0 to 8.5% (average 5.7%). Recoveries of indium added to various samples ranged from 96.7 to 105.6% (average 100.2%). ?? 1984.

  12. Spatial Distribution of Uranium in Groundwater and Associated Geologic Material at the NABIR Field Research Center Site, Oak Ridge, Tennessee

    NASA Astrophysics Data System (ADS)

    Phillips, D. H.; Watson, D. B.

    2001-05-01

    The Natural and Accelerated Bioremediation Research Program (NABIR) has established a Field Research Center (FRC) on the Oak Ridge Reservation in Oak Ridge, Tennessee. The FRC provides a site for investigators to conduct research and obtain samples related to in situ bioremediation. This site is in the form of four buried unlined ponds where uranium and other contaminants were disposed in nitric acid for 32 years. In 1984, the ponds were neutralized with limestone, RCRA capped and paved with a parking lot. Analysis of groundwater and geologic material sampled from the site show that uranium is preferentially migrating away from the ponds and towards the nearby Bear Creek. Preferential flow appears to be associated with an ancient buried stream bed and remnant fractures in the saprolite where the uranium content of the groundwater is as high as 7 ppm. Due to the greater discharge of the contaminant source in this portion of the regolith, there is higher weathering of the shallow regolith (top 20 ft)and a greater accumulation of uranium compared to other sections of geologic material surrounding the disposal site.

  13. Determining the hydraulic properties of saturated, low-permeability geological materials in the laboratory: Advances in theory and practice

    USGS Publications Warehouse

    Zhang, M.; Takahashi, M.; Morin, R.H.; Endo, H.; Esaki, T.; ,

    2002-01-01

    The accurate hydraulic characterization of low-permeability subsurface environments has important practical significance. In order to examine this issue from the perspective of laboratory-based approaches, we review some recent advancements in the theoretical analyses of three different laboratory techniques specifically applied to low-permeability geologic materials: constant-head, constant flow-rate and transient-pulse permeability tests. Some potential strategies for effectively decreasing the time required to confidently estimate the permeability of these materials are presented. In addition, a new and versatile laboratory system is introduced that can implement any of these three test methods while simultaneously subjecting a specimen to high confining pressures and pore pressures, thereby simulating in situ conditions at great depths. The capabilities and advantages of this innovative system are demonstrated using experimental data derived from Shirahama sandstone and Inada granite, two rock types widely encountered in Japan.

  14. Determination of palladium, platinum and rhodium in geologic materials by fire assay and emission spectrography

    USGS Publications Warehouse

    Hapfty, J.; Riley, L.B.

    1968-01-01

    A method is described for the determination of palladium down to 4ppb (parts per billion, 109), platinum down to 10 ppb and rhodium down to 5 ppb in 15 g of sample. Fire-assay techniques are used to preconcentrate the platinum metals into a gold bead, then the bead is dissolved in aqua regia and diluted to volume with 1M hydrochloric acid. The solution is analysed by optical emission spectrography of the residue from 200 ??l of it evaporated on a pair of flat-top graphite electrodes. This method requires much less sample handling than most published methods for these elements. Data are presented for G-1, W-1, and six new standard rocks of the U.S. Geological Survey. The values for palladium in W-1 are in reasonable agreement with previously published data. ?? 1968.

  15. Characterizing weathering intensity and trends of geological materials in the Gilgel Gibe catchment, southwestern Ethiopia

    NASA Astrophysics Data System (ADS)

    Regassa, Alemayehu; Van Daele, K.; De Paepe, P.; Dumon, M.; Deckers, J.; Asrat, Asfawossen; Van Ranst, E.

    2014-11-01

    Detailed geological and geochemical characterization is crucial to support soil studies in such geologically and topographically complex systems as the Gilgel Gibe catchment in southwestern Ethiopia. Field studies, as well as mineralogical, petrological and geochemical analyses on selected rock samples and their weathering products revealed that the catchment is dominantly underlain by rhyolites and trachytes, which occur as both lava flows and pyroclastic associations. Most of the lavas have a trachytic texture, while few others are massive or show spherulitic or perlitic texture. The rocks have a SiO2-content ranging from about 62 to 73 wt% (intermediate to felsic composition, on an anhydrous base) and a relatively high Na2O + K2O content ranging from about 9 to 12 wt% (anhydrous base). The dominant phenocrysts present in the rocks are plagioclase, sanidine and Fe-Ti oxide minerals. Alkali-rich amphiboles and quartz occur in most of them, while hornblende, titanite and clinopyroxene are rare. The amount of phenocrysts varies from less than 1 vol.% to about 30 vol.%. The pyroclastic associations are discontinuously scattered within the study area. They all have a glassy matrix (vitrophyric texture) and are composed of a mixture of lithics, crystals and glass. In comparison with the lava samples, the pyroclastic samples exhibit a more variable chemistry. In contrast, the X-ray diffractograms of the pyroclastic deposits and the lavas show little difference. The Chemical Index of Alteration values for the studied samples vary from 53 to 99 indicating moderate to high intensity of weathering. Samples from lava flows have shown less degree of weathering than samples of the pyroclastic associations.

  16. Development of a reference material of a single DNA molecule for the quality control of PCR testing.

    PubMed

    Mano, Junichi; Hatano, Shuko; Futo, Satoshi; Yoshii, Junji; Nakae, Hiroki; Naito, Shigehiro; Takabatake, Reona; Kitta, Kazumi

    2014-09-01

    We developed a reference material of a single DNA molecule with a specific nucleotide sequence. The double-strand linear DNA which has PCR target sequences at the both ends was prepared as a reference DNA molecule, and we named the PCR targets on each side as confirmation sequence and standard sequence. The highly diluted solution of the reference molecule was dispensed into 96 wells of a plastic PCR plate to make the average number of molecules in a well below one. Subsequently, the presence or absence of the reference molecule in each well was checked by real-time PCR targeting for the confirmation sequence. After an enzymatic treatment of the reaction mixture in the positive wells for the digestion of PCR products, the resultant solution was used as the reference material of a single DNA molecule with the standard sequence. PCR analyses revealed that the prepared samples included only one reference molecule with high probability. The single-molecule reference material developed in this study will be useful for the absolute evaluation of a detection limit of PCR-based testing methods, the quality control of PCR analyses, performance evaluations of PCR reagents and instruments, and the preparation of an accurate calibration curve for real-time PCR quantitation.

  17. Development of a reference material of a single DNA molecule for the quality control of PCR testing.

    PubMed

    Mano, Junichi; Hatano, Shuko; Futo, Satoshi; Yoshii, Junji; Nakae, Hiroki; Naito, Shigehiro; Takabatake, Reona; Kitta, Kazumi

    2014-09-01

    We developed a reference material of a single DNA molecule with a specific nucleotide sequence. The double-strand linear DNA which has PCR target sequences at the both ends was prepared as a reference DNA molecule, and we named the PCR targets on each side as confirmation sequence and standard sequence. The highly diluted solution of the reference molecule was dispensed into 96 wells of a plastic PCR plate to make the average number of molecules in a well below one. Subsequently, the presence or absence of the reference molecule in each well was checked by real-time PCR targeting for the confirmation sequence. After an enzymatic treatment of the reaction mixture in the positive wells for the digestion of PCR products, the resultant solution was used as the reference material of a single DNA molecule with the standard sequence. PCR analyses revealed that the prepared samples included only one reference molecule with high probability. The single-molecule reference material developed in this study will be useful for the absolute evaluation of a detection limit of PCR-based testing methods, the quality control of PCR analyses, performance evaluations of PCR reagents and instruments, and the preparation of an accurate calibration curve for real-time PCR quantitation. PMID:25061686

  18. Retrospective Analysis of NIST Standard Reference Material 1450, Fibrous Glass Board, for Thermal Insulation Measurements.

    PubMed

    Zarr, Robert R; Heckert, N Alan; Leigh, Stefan D

    2014-01-01

    Thermal conductivity data acquired previously for the establishment of Standard Reference Material (SRM) 1450, Fibrous Glass Board, as well as subsequent renewals 1450a, 1450b, 1450c, and 1450d, are re-analyzed collectively and as individual data sets. Additional data sets for proto-1450 material lots are also included in the analysis. The data cover 36 years of activity by the National Institute of Standards and Technology (NIST) in developing and providing thermal insulation SRMs, specifically high-density molded fibrous-glass board, to the public. Collectively, the data sets cover two nominal thicknesses of 13 mm and 25 mm, bulk densities from 60 kg·m(-3) to 180 kg·m(-3), and mean temperatures from 100 K to 340 K. The analysis repetitively fits six models to the individual data sets. The most general form of the nested set of multilinear models used is given in the following equation: [Formula: see text]where λ(ρ,T) is the predicted thermal conductivity (W·m(-1)·K(-1)), ρ is the bulk density (kg·m(-3)), T is the mean temperature (K) and ai (for i = 1, 2, … 6) are the regression coefficients. The least squares fit results for each model across all data sets are analyzed using both graphical and analytic techniques. The prevailing generic model for the majority of data sets is the bilinear model in ρ and T. [Formula: see text] One data set supports the inclusion of a cubic temperature term and two data sets with low-temperature data support the inclusion of an exponential term in T to improve the model predictions. Physical interpretations of the model function terms are described. Recommendations for future renewals of SRM 1450 are provided. An Addendum provides historical background on the origin of this SRM and the influence of the SRM on external measurement programs.

  19. A geological study of clayey laterite and clayey hydromorphic material of the region of Yaoundé (Cameroon): a prerequisite for local material promotion

    NASA Astrophysics Data System (ADS)

    Ngon Ngon, G. F.; Yongue–Fouateu, R.; Bitom, D. L.; Bilong, P.

    2009-09-01

    A geological survey carried out in the Yaoundé (Cameroon) region has revealed the presence of homogeneous clayey laterite in the upper part of a laterite cover on interfluves, thickest on hills (780-800 m altitude) where ferricrete is absent, and clayey heterogeneous hydromorphic material in valleys. We present in this paper the physical, mineralogical and geochemical properties of these occurrences and discuss their potential as raw material for pottery, manufacture of bricks and tiles. These clayey raw materials are mostly made up of fine particles (ranging from 55 to 60% clay + silt in the clayey laterite, more than 70% clay + silt in the clayey hydromorphic material). Their chemical composition is characterized by silica (<60% SiO 2), alumina (<35% Al 2O 3) and iron (ranging from 3 to 14% Fe 2O 3). Their main clay minerals are disorganized and poorly crystallized kaolinites. The average limits of liquidity (44.56% versus 91.58%) and limits of plasticity (22.4 versus 45.93) revealed that clayey hydromorphic material has the greatest plasticity. The studied raw materials are suitable for making pottery as well as the manufacture of bricks and tiles. However, the high iron content in the clayey laterite (between 11 and 12% Fe 2O 3) prevents their efficient use in the manufacture of ceramics.

  20. Use of ceramic materials in waste-package systems for geologic disposal of nuclear wastes

    SciTech Connect

    Fullam, H.T.

    1980-12-01

    A study to investigate the potential use of ceramic materials as components in the waste package systems was conducted. The initial objective of the study was to screen and compare a large number of ceramic materials and identify the best materials for the proposed application. The principal method used to screen the candidates was to subject samples of each material to a series of leaching tests and to determine their relative resistance to attack by the leach solutions. A total of 14 ceramic materials, plus graphite and basalt were evaluated using three different leach solutions: demineralized water, a synthetic Hanford ground water, and a synthetic WIPP brine solution. The ceramic materials screened were Al/sub 2/O/sub 3/ (99%), Al/sub 2/O/sub 3/ (99.8%), mullite (2Al/sub 2/O/sub 3/.SiO/sub 2/), vitreous silica (SiO/sub 2/), BaTiO/sub 3/, CaTiO/sub 3/, CaTiSiO/sub 5/, TiO/sub 2/, ZrO/sub 2/, ZrSiO/sub 4/, Pyroceram 9617, and Marcor Code 9658 machinable glass-ceramic. Average leach rates for the materials tested were determined from analyses of the leach solutions and/or sample weight loss measurements. Because of the limited scope of the present study, evaluation of the specimens was limited to ceramographic examination. Based on an overall evaluation of the leach rate data, five of the materials tested, namely graphite, TiO/sub 2/, ZrO/sub 2/, and the two grades of alumina, exhibited much greater resistance to leaching than did the other materials tested. Based on all the experimental data obtained, and considering other factors such as cost, availability, fabrication technology, and mechanical and physical properties, graphite and alumina are the preferred candidates for the barrier application. The secondary choices are TiO/sub 2/ and ZrO/sub 2/.