Science.gov

Sample records for fine chemicals iv

  1. Chemical and magnetic properties of rapidly cooled metastable ferri-ilmenite solid solutions - IV: the fine structure of self-reversed thermoremanent magnetization

    NASA Astrophysics Data System (ADS)

    Robinson, Peter; McEnroe, S. A.; Fabian, K.; Harrison, R. J.; Thomas, C. I.; Mukai, H.

    2014-03-01

    Magnetic experiments, a Monte Carlo simulation and transmission electron microscopy observations combine to confirm variable chemical phase separation during quench and annealing of metastable ferri-ilmenite compositions, caused by inhomogeneous Fe-Ti ordering and anti-ordering. Separation begins near interfaces between growing ordered and anti-ordered domains, the latter becoming progressively enriched in ilmenite component, moving the Ti-impoverished hematite component into Fe-enriched diffusion waves near the interfaces. Even when disordered regions are eliminated, Fe-enriched waves persist and enlarge on anti-phase boundaries between growing and shrinking ordered and anti-ordered domains. Magnetic results and conceptual models show that magnetic ordering with falling T initiates in the Fe-enriched wave crests. Although representing only a tiny fraction of material, identified at highest Ts on a field-cooling curve, they control the `pre-destiny' of progressive magnetization at lower T. They can provide a positive magnetic moment in a minority of ordered ferrimagnetic material, which, by exchange coupling, then creates a self-reversed negative moment in the remaining majority. Four Ts or T ranges are recognized on typical field-cooling curves: TPD is the T range of `pre-destination'; TC is the predominant Curie T where major positive magnetization increases sharply; TMAX is where magnetization reaches a positive maximum, beyond which it is outweighed by self-reversed magnetization and TZM is the T where total magnetization passes zero. Disposition of these Ts on cooling curves indicate the fine structure of self-reversed thermoremanent magnetization. These results confirm much earlier suspicions that the `x-phase' responsible for self-reversed magnetization resides in Fe-enriched phase boundaries.

  2. Chemical composition of Martian fines

    NASA Technical Reports Server (NTRS)

    Clark, B. C.; Baird, A. K.; Weldon, R. J.; Tsusaki, D. M.; Schnabel, L.; Candelaria, M. P.

    1982-01-01

    Of the 21 samples acquired for the Viking X-ray fluorescence spectrometer, 17 were analyzed to high precision. Compared to typical terrestrial continental soils and lunar mare fines, the Martian fines are lower in Al, higher in Fe, and much higher in S and Cl concentrations. Protected fines at the two lander sites are almost indistinguishable, but concentration of the element S is somewhat higher at Utopia. Duricrust fragments, successfully acquired only at the Chryse site, invariably contained about 50% higher S than fines. No elements correlate positively with S, except Cl and possibly Mg. A sympathetic variation is found among the triad Si, Al, Ca; positive correlation occurs between Ti and Fe. Sample variabilities are as great within a few meters as between lander locations (4500 km apart), implying the existence of a universal Martian regolith component of constant average composition. The nature of the source materials for the regolith fines must be mafic to ultramafic.

  3. The production of fine chemicals by biotransformations.

    PubMed

    Straathof, Adrie J J; Panke, Sven; Schmid, Andreas

    2002-12-01

    Today, biocatalysis is a standard technology for the production of chemicals. An analysis of 134 industrial biotransformations reveals that hydrolases (44%) and redox biocatalysts (30%) are the most prominent categories. Most products are chiral (89%) and are used as fine chemicals. In the chemical industry, successful product developments involve on average a yield of 78%, a volumetric productivity of 15.5 g/(L.h) and a final product concentration of 108 g/L. By contrast, the pharmaceutical industry focuses on time-to-market. The implications of this for future research and development on biocatalysis are discussed.

  4. Enhanced control of fine particles following Title IV coal switching and NOx control

    SciTech Connect

    Durham, M.D.; Baldrey, K.E.; Bustard, C.J.; Martin, C.

    1997-12-31

    Electrostatic precipitators (ESPs) serve as the primary particle control devices for a majority of coal-fired power generating units in the United States. ESPs are used to collect particulate matter that range in size from less than one micrometer in diameter to several hundred micrometers. Many of the options that utilities will use to respond to Title IV of the 1990 Clean Air Act Amendments will result in changes to the ash that will be detrimental to the performance of the ESP causing increased emissions of fine particles and higher opacity. For example, a switch to low-sulfur coal significantly increases particle resistivity while low-NO{sub x} burners increase the carbon content of ashes. Both of these changes could result in derating of the boiler to comply with emissions standards. ADA has developed a chemical additive that is designed to improve the operation of ESI`s to bring these systems into compliance operation without the need for expensive capital modifications. The additives provide advantages over competing technologies in terms of low capital cost, easy to handle chemicals, and relatively non-toxic chemicals. In addition, the new additive is insensitive to ash chemistry which will allow the utility complete flexibility to select the most economical coal. Results from full-scale and pilot plant demonstrations are reported.

  5. [Starting with camphor--the progress of Nippon Fine Chemical].

    PubMed

    Kimura, Osamu

    2010-01-01

    In 1918, Nippon Fine Chemical Co., Ltd. (NFC) was founded under the name, Nippon Camphor Co., Ltd. for the purpose of unifying the camphor business throughout Japan. The company manufactured purified camphor as a government-monopolized good. Camphor was used as a plasticizer for nitrocellulose, as a moth repellent, as an antimicrobial substance, as a rust inhibitor, and as an active ingredient in medicine. It was also a very important good exported in order to obtain foreign currency. Later on, after World War II and the abolition of the camphor monopoly, the company started manufacturing products related to oils and fats, including higher fatty acids, and expanded its business by developing a new field of chemical industry. In 1971 the company changed its name to Nippon Fine Chemical Co., Ltd., and made a new start as a diversified fine chemicals company. Recently, the fine chemicals division of NFC has concentrated on rather complex molecules, such as active pharmaceutical ingredients, and other chemicals. Since 2000, NFC have started to supply "Presome", precursors of liposome DDS drugs. NFC is strengthening marketing strategies in foreign countries with unique technologies and products.

  6. Catalytic upgrading of butyric acid towards fine chemicals and biofuels

    PubMed Central

    Sjöblom, Magnus; Matsakas, Leonidas; Christakopoulos, Paul; Rova, Ulrika

    2016-01-01

    Fermentation-based production of butyric acid is robust and efficient. Modern catalytic technologies make it possible to convert butyric acid to important fine chemicals and biofuels. Here, current chemocatalytic and biocatalytic conversion methods are reviewed with a focus on upgrading butyric acid to 1-butanol or butyl-butyrate. Supported Ruthenium- and Platinum-based catalyst and lipase exhibit important activities which can pave the way for more sustainable process concepts for the production of green fuels and chemicals. PMID:26994015

  7. New trends in (heterogeneous) catalysis for the fine chemicals industry.

    PubMed

    Bonrath, Werner

    2014-01-01

    New catalytic methods and modern trends for the synthesis of fine chemicals, especially vitamins, carotenoids, flavoring and fragrance compounds are presented. In particular the application of heterogeneous catalysis in the formation and production on industrial scale of these classes of organic compounds will be highlighted and its use in the replacement of former stoichiometric processes.

  8. Fine particulate chemical composition and light extinction at Meadview, AZ.

    PubMed

    Eatough, Delbert J; Cui, Wenxuan; Hull, Jeffery; Farber, Robert J

    2006-12-01

    The concentration of fine particulate nitrate, sulfate, and carbonaceous material was measured for 12-hr day-night samples using diffusion denuder samplers during the Project Measurement of Haze and Visibility Effects (MOHAVE) July to August 1992 Summer Intensive study at Meadview, AZ, just west of Grand Canyon National Park. Organic material was measured by several techniques. Only the diffusion denuder method measured the semivolatile organic material. Fine particulate sulfate and nitrate (using denuder technology) determined by various groups agreed. Based on the various collocated measurements obtained during the Project MOHAVE study, the precision of the major fine particulate species was +/- 0.6 microg/m3 organic material, +/- 0.3 microg/m3 ammonium sulfate, and +/- 0.07 microg/m3 ammonium nitrate. Data were also available on fine particulate crustal material, fine and coarse particulate mass from the Interagency Monitoring of Protected Visual Environments sampling system, and relative humidity (RH), light absorption, particle scattering, and light extinction measurements from Project MOHAVE. An extinction budget was obtained using mass scattering coefficients estimated from particle size distribution data. Literature data were used to estimate the change in the mass scattering coefficients for the measured species as a function of RH and for the absorption of light by elemental carbon. Fine particulate organic material was the principal particulate contributor to light extinction during the study period, with fine particulate sulfate as the second most important contributor. During periods of highest light extinction, contributions from fine particulate organic material, sulfate, and light-absorbing carbon dominated the extinction of light by particles. Particle light extinction was dominated by sulfate and organic material during periods of lowest light extinction. Combination of the extinction data and chemical mass balance analysis of sulfur oxides

  9. Fine particulate chemical composition and light extinction at Meadview, AZ

    SciTech Connect

    Delbert J. Eatough; Wenxuan Cui; Jeffery Hull; Robert J. Farber

    2006-12-15

    The concentration of fine particulate nitrate, sulfate, and carbonaceous material was measured for 12-hr daynight samples using diffusion denuder samplers during the Project Measurement of Haze and Visibility Effects (MOHAVE) July to August 1992 Summer Intensive study at Meadview, AZ, just west of Grand Canyon National Park. Organic material was measured by several techniques. Only the diffusion denuder method measured the semivolatile organic material. Fine particulate sulfate and nitrate (using denuder technology) determined by various groups agreed. Based on the various collocated measurements obtained during the Project MOHAVE study, the precision of the major fine particulate species was {+-} 0.6 {mu}g/m{sup 3} organic material, {+-} 0.3 {mu}g/m{sup 3} ammonium sulfate, and {+-} 0.07 {mu}g/m{sup 3} ammonium nitrate. Fine particulate organic material was the principal particulate contributor to light extinction during the study period, with fine particulate sulfate as the second most important contributor. Particle light extinction was dominated by sulfate and organic material during periods of lowest light extinction. Combination of the extinction data and chemical mass balance analysis of sulfur oxides sources in the region indicate that the major anthropogenic contributors to light extinction were from the Los Angeles, CA, and Las Vegas, NV, urban areas. Mohave Power Project associated secondary sulfate was a negligible contributor to light extinction. 49 refs., 12 figs., 7 tabs.

  10. Catalytic conversion of lignocellulosic biomass to fine chemicals and fuels.

    PubMed

    Zhou, Chun-Hui; Xia, Xi; Lin, Chun-Xiang; Tong, Dong-Shen; Beltramini, Jorge

    2011-11-01

    Lignocellulosic biomass is the most abundant and bio-renewable resource with great potential for sustainable production of chemicals and fuels. This critical review provides insights into the state-of the-art accomplishments in the chemocatalytic technologies to generate fuels and value-added chemicals from lignocellulosic biomass, with an emphasis on its major component, cellulose. Catalytic hydrolysis, solvolysis, liquefaction, pyrolysis, gasification, hydrogenolysis and hydrogenation are the major processes presently studied. Regarding catalytic hydrolysis, the acid catalysts cover inorganic or organic acids and various solid acids such as sulfonated carbon, zeolites, heteropolyacids and oxides. Liquefaction and fast pyrolysis of cellulose are primarily conducted over catalysts with proper acidity/basicity. Gasification is typically conducted over supported noble metal catalysts. Reaction conditions, solvents and catalysts are the prime factors that affect the yield and composition of the target products. Most of processes yield a complex mixture, leading to problematic upgrading and separation. An emerging technique is to integrate hydrolysis, liquefaction or pyrolysis with hydrogenation over multifunctional solid catalysts to convert lignocellulosic biomass to value-added fine chemicals and bio-hydrocarbon fuels. And the promising catalysts might be supported transition metal catalysts and zeolite-related materials. There still exist technological barriers that need to be overcome (229 references). This journal is © The Royal Society of Chemistry 2011

  11. Yeast cell factories for fine chemical and API production

    PubMed Central

    Pscheidt, Beate; Glieder, Anton

    2008-01-01

    This review gives an overview of different yeast strains and enzyme classes involved in yeast whole-cell biotransformations. A focus was put on the synthesis of compounds for fine chemical and API (= active pharmaceutical ingredient) production employing single or only few-step enzymatic reactions. Accounting for recent success stories in metabolic engineering, the construction and use of synthetic pathways was also highlighted. Examples from academia and industry and advances in the field of designed yeast strain construction demonstrate the broad significance of yeast whole-cell applications. In addition to Saccharomyces cerevisiae, alternative yeast whole-cell biocatalysts are discussed such as Candida sp., Cryptococcus sp., Geotrichum sp., Issatchenkia sp., Kloeckera sp., Kluyveromyces sp., Pichia sp. (including Hansenula polymorpha = P. angusta), Rhodotorula sp., Rhodosporidium sp., alternative Saccharomyces sp., Schizosaccharomyces pombe, Torulopsis sp., Trichosporon sp., Trigonopsis variabilis, Yarrowia lipolytica and Zygosaccharomyces rouxii. PMID:18684335

  12. Yeast cell factories for fine chemical and API production.

    PubMed

    Pscheidt, Beate; Glieder, Anton

    2008-08-07

    This review gives an overview of different yeast strains and enzyme classes involved in yeast whole-cell biotransformations. A focus was put on the synthesis of compounds for fine chemical and API (= active pharmaceutical ingredient) production employing single or only few-step enzymatic reactions. Accounting for recent success stories in metabolic engineering, the construction and use of synthetic pathways was also highlighted. Examples from academia and industry and advances in the field of designed yeast strain construction demonstrate the broad significance of yeast whole-cell applications. In addition to Saccharomyces cerevisiae, alternative yeast whole-cell biocatalysts are discussed such as Candida sp., Cryptococcus sp., Geotrichum sp., Issatchenkia sp., Kloeckera sp., Kluyveromyces sp., Pichia sp. (including Hansenula polymorpha = P. angusta), Rhodotorula sp., Rhodosporidium sp., alternative Saccharomyces sp., Schizosaccharomyces pombe, Torulopsis sp., Trichosporon sp., Trigonopsis variabilis, Yarrowia lipolytica and Zygosaccharomyces rouxii.

  13. Calcium, Strontium and Barium Homogeneous Catalysts for Fine Chemicals Synthesis.

    PubMed

    Sarazin, Yann; Carpentier, Jean-François

    2016-12-01

    The large alkaline earths (Ae), calcium, strontium and barium, have in the past 15 years yielded a brand new generation of heteroleptic molecular catalysts for the production of fine chemicals. However, the integrity of these complexes is often plagued by ligand redistribution equilibria in solution. This personal account retraces the paths followed in our research group towards the design of stable heteroleptic alkalino-earth complexes, including the use of intramolecular noncovalent Ae···H-Si and Ae···F-C interactions. Their implementation as homogenous precatalysts for reactions such as the intramolecular and intermolecular hydroamination and hydrophosphination of activated alkenes, the hydrophosphonylation of ketones, and the dehydrogenative coupling of amines and hydrosilanes that enable the efficient and controlled formations of CP, CN, or SiN σ-bonds, is presented in a synthetic perspective that highlights their overall outstanding catalytic performance. © 2016 The Chemical Society of Japan & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  14. A 'Fine' chemical industry for life science products: green solutions to chemical challenges.

    PubMed

    Bruggink, A; Straathof, A J J; van der Wielen, L A M

    2003-01-01

    Modern biotechnology, in combination with chemistry and process technology, is crucial for the development of new clean and cost effective manufacturing concepts for fine-chemical, food specialty and pharmaceutical products. The impact of biocatalysis on the fine-chemicals industry is presented, where reduction of process development time, the number of reaction steps and the amount of waste generated per kg of end product are the main targets. Integration of biosynthesis and organic chemistry is seen as a key development. The advances in bioseparation technology need to keep pace with the rate of development of novel bio- or chemocatalytic process routes with revised demands on process technology. The need for novel integrated reactors is also presented. The necessary acceleration of process development and reduction of the time-to-market seem well possible, particularly by integrating high-speed experimental techniques and predictive modelling tools. This is crucial for the development of a more sustainable fine-chemicals industry. The evolution of novel 'green' production routes for semi-synthetic antibiotics (SSAs) that are replacing existing chemical processes serves as a recent and relevant case study of this ongoing integration of disciplines. We will also show some challenges in this specific field.

  15. Combined Chemical Activation and Fenton Degradation to Convert Waste Polyethylene into High-Value Fine Chemicals.

    PubMed

    Chow, Cheuk-Fai; Wong, Wing-Leung; Ho, Keith Yat-Fung; Chan, Chung-Sum; Gong, Cheng-Bin

    2016-07-04

    Plastic waste is a valuable organic resource. However, proper technologies to recover usable materials from plastic are still very rare. Although the conversion/cracking/degradation of certain plastics into chemicals has drawn much attention, effective and selective cracking of the major waste plastic polyethylene is extremely difficult, with degradation of C-C/C-H bonds identified as the bottleneck. Pyrolysis, for example, is a nonselective degradation method used to crack plastics, but it requires a very high energy input. To solve the current plastic pollution crisis, more effective technologies are needed for converting plastic waste into useful substances that can be fed into the energy cycle or used to produce fine chemicals for industry. In this study, we demonstrate a new and effective chemical approach by using the Fenton reaction to convert polyethylene plastic waste into carboxylic acids under ambient conditions. Understanding the fundamentals of this new chemical process provides a possible protocol to solve global plastic-waste problems.

  16. 78 FR 69134 - Manufacturer of Controlled Substances; Notice of Registration: AMPAC Fine Chemicals, LLC.

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-11-18

    ... Enforcement Administration Manufacturer of Controlled Substances; Notice of Registration: AMPAC Fine Chemicals, LLC. By Notice dated July 23, 2013, and published in the Federal Register on July 31, 2013, 78 FR 46372, AMPAC Fine Chemicals, LLC., Highway 50 and Hazel Avenue, Building 05001, Rancho...

  17. Relativistic calculations of radiative properties and fine structure constant varying sensitivity coefficients in the astrophysically relevant Zn II, Si IV and Ti IV ions

    NASA Astrophysics Data System (ADS)

    Nandy, D. K.; Sahoo, B. K.

    2015-03-01

    We have carried out calculations of the relativistic sensitivity coefficients, oscillator strengths, transition probabilities, lifetimes and magnetic dipole hyperfine structure constants for a number of low-lying states in the Zn II, Si IV and Ti IV ions which are abundant in the distant quasars and various stellar plasmas. These spectroscopic data will be very useful for probing temporal variation of the fine structure constant (αe) and in the diagnostic processes of some of the astrophysical plasmas. We have employed all-order perturbative methods in the relativistic coupled-cluster framework using the Dirac-Coulomb Hamiltonian to calculate the atomic wavefunctions of the considered ions. Reference states are constructed with the VN-1 and VN+1 potentials and then the electron-electron correlation effects are taken into account by constructing all possible singly and doubly excited configurations, involving both the core and valence electrons, from the respective reference states. We have also determined one electron affinities and ionization potentials of many excited states in these Zn II, Si IV and Ti IV ions. Except for a few states we have attained accuracies within 1 per cent for the energies compared with their experimental values. Our calculated sensitivity coefficients are estimated to have similar accuracies as of the calculated energies. Furthermore, combining our calculated transition matrix elements with the experimental wavelengths we evaluate transition probabilities, oscillator strengths and lifetimes of some of the excited states in these ions. These results are compared with the available data in a few cases and found to be in very good agreement among themselves. Using our reported hyperfine structure constants due to the dominant magnetic dipole interaction, it is possible to determine hyperfine splittings approximately in the above considered ions.

  18. Finely Tuned Asymmetric Platinum(IV) Anticancer Complexes: Structure-Activity Relationship and Application as Orally Available Prodrugs.

    PubMed

    Yap, Siew Qi; Chin, Chee Fei; Hong Thng, Agnes Hwee; Pang, Yi Yun; Ho, Han Kiat; Ang, Wee Han

    2017-02-20

    Platinum(IV) bis-carboxylates are highly versatile prodrug scaffolds with different axial ligands that can be functionalized while keeping the platinum(II) pharmacophore intact. Using a sequential acylation strategy, we developed a class of Pt(IV) prodrugs of cisplatin with contrasting lipophilic and hydrophilic ligands. We investigated their stability, reduction rates, lipophilicity, aqueous solubility, and antiproliferative efficacies, and assessed for correlations among the parameters that could be useful in drug design. We showed that compounds with high lipophilicity result in better antiproliferative effects in vitro and in vivo, with one of the three compounds tested showing better efficacy than satraplatin against an animal model of colorectal cancer, owing to its higher solubility and lower reduction rates. Our asymmetric Pt(IV) prodrugs may pave the way for a highly predictable, fine-tuned class of orally available Pt(IV) prodrugs for the treatment of colorectal cancer. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. Enhancing of chemical compound and drug name recognition using representative tag scheme and fine-grained tokenization

    PubMed Central

    2015-01-01

    Background The functions of chemical compounds and drugs that affect biological processes and their particular effect on the onset and treatment of diseases have attracted increasing interest with the advancement of research in the life sciences. To extract knowledge from the extensive literatures on such compounds and drugs, the organizers of BioCreative IV administered the CHEMical Compound and Drug Named Entity Recognition (CHEMDNER) task to establish a standard dataset for evaluating state-of-the-art chemical entity recognition methods. Methods This study introduces the approach of our CHEMDNER system. Instead of emphasizing the development of novel feature sets for machine learning, this study investigates the effect of various tag schemes on the recognition of the names of chemicals and drugs by using conditional random fields. Experiments were conducted using combinations of different tokenization strategies and tag schemes to investigate the effects of tag set selection and tokenization method on the CHEMDNER task. Results This study presents the performance of CHEMDNER of three more representative tag schemes-IOBE, IOBES, and IOB12E-when applied to a widely utilized IOB tag set and combined with the coarse-/fine-grained tokenization methods. The experimental results thus reveal that the fine-grained tokenization strategy performance best in terms of precision, recall and F-scores when the IOBES tag set was utilized. The IOBES model with fine-grained tokenization yielded the best-F-scores in the six chemical entity categories other than the "Multiple" entity category. Nonetheless, no significant improvement was observed when a more representative tag schemes was used with the coarse or fine-grained tokenization rules. The best F-scores that were achieved using the developed system on the test dataset of the CHEMDNER task were 0.833 and 0.815 for the chemical documents indexing and the chemical entity mention recognition tasks, respectively. Conclusions The

  20. Development of bio-based fine chemical production through synthetic bioengineering.

    PubMed

    Hara, Kiyotaka Y; Araki, Michihiro; Okai, Naoko; Wakai, Satoshi; Hasunuma, Tomohisa; Kondo, Akihiko

    2014-12-14

    Fine chemicals that are physiologically active, such as pharmaceuticals, cosmetics, nutritional supplements, flavoring agents as well as additives for foods, feed, and fertilizer are produced by enzymatically or through microbial fermentation. The identification of enzymes that catalyze the target reaction makes possible the enzymatic synthesis of the desired fine chemical. The genes encoding these enzymes are then introduced into suitable microbial hosts that are cultured with inexpensive, naturally abundant carbon sources, and other nutrients. Metabolic engineering create efficient microbial cell factories for producing chemicals at higher yields. Molecular genetic techniques are then used to optimize metabolic pathways of genetically and metabolically well-characterized hosts. Synthetic bioengineering represents a novel approach to employ a combination of computer simulation and metabolic analysis to design artificial metabolic pathways suitable for mass production of target chemicals in host strains. In the present review, we summarize recent studies on bio-based fine chemical production and assess the potential of synthetic bioengineering for further improving their productivity.

  1. [Applications of nitrile converting enzymes in the production of fine chemicals].

    PubMed

    Zheng, Yuguo; Xue, Yaping; Liu, Zhiqiang; Zheng, Renchao; Shen, Yinchu

    2009-12-01

    Nitriles are an important type of synthetic intermediates in the production of fine chemicals because of their easy preparations and versatile transformations. The traditional chemical conversion of nitriles to carboxylic acids and amides is feasible but it requires relatively harsh conditions of heat, acid or alkali. Nitrile converting enzymes (nitrilase, nitrile hydratase and amidase) which are used as biocatalyst for the production of fine chemicals have attracted substantial interest because of their ability to convert readily available nitriles into the corresponding higher value amides or acids under mild conditions with excellent chemo-, regio- and stereo-selectivities. Many nitrile converting enzymes have been explored and widely used for the production of fine chemicals. In this paper, various examples of biocatalytic synthesis of pharmaceuticals and their intermediates, agrochemicals and their intermediates, food and feed additives, and other fine chemicals are presented. In the near future, an increasing number of novel nitrile converting enzymes will be screened and their potential in the production of useful fine chemicals will be further exploited.

  2. Enhanced sensitivity to the fine-structure-constant variation in the Th IV atomic clock transition

    SciTech Connect

    Flambaum, V. V.; Porsev, S. G.

    2009-12-15

    Our calculations have shown that the 5f{sub 5/2}-7s{sub 1/2} 23 131 cm{sup -1} transition from the ground state in the ion Th{sup 3+} is very sensitive to the temporal variation of the fine-structure constant alpha=e{sup 2}/(Planck constant/2pi)c (q=-75 300 cm{sup -1}). The line is very narrow, the ion has been trapped and laser cooled, and the positive shifter line 5f{sub 5/2}-5f{sub 7/2} 4325 cm{sup -1} (q=+2900 cm{sup -1}) may be used as a reference. A comparison may also be made with a positive shifter in another atom or ion. This makes Th{sup 3+} a good candidate to search for the alpha variation.

  3. Towards novel processes for the fine-chemical and pharmaceutical industries.

    PubMed

    Huisman, Gjalt W; Gray, David

    2002-08-01

    In response to the need in the pharmaceutical industry for more complex, chiral molecules, fine-chemical companies are embracing new manufacturing technologies to produce compounds of these specifications. In particular, recent developments in biocatalysis combined with novel process engineering are providing improved methods for the production of valuable chemical intermediates.

  4. Trends and innovations in industrial biocatalysis for the production of fine chemicals.

    PubMed

    Panke, Sven; Held, Martin; Wubbolts, Marcel

    2004-08-01

    Biocatalysis has become an established technology for the industrial manufacture of fine chemicals. In recent years, a multitude of chemical companies have embraced biocatalysis for the manufacture of desired stereoisomers, and new or improved methods for the synthesis of enantiomerically pure alpha- and beta-amino acids, amines, amides, peptides, nitriles, alcohols, organic acids and epoxides have emerged. Furthermore, the selectivity and mild operational conditions of biocatalysts are increasingly applied in industry to modify complex target molecules. These recent innovations in the manufacture of industrial fine chemicals using biocatalysis are discussed from an industrial perspective.

  5. Creating pathways towards aromatic building blocks and fine chemicals.

    PubMed

    Thompson, Brian; Machas, Michael; Nielsen, David R

    2015-12-01

    Aromatic compounds represent a broad class of chemicals with a range of industrial applications, all of which are conventionally derived from petroleum feedstocks. However, owing to a diversity of available pathway precursors along with natural and engineered enzyme 'parts', microbial cell factories can be engineered to create alternative, renewable routes to many of the same aromatic products. Drawing from the latest tools and strategies in metabolic engineering and synthetic biology, such efforts are becoming an increasingly systematic practice, while continued efforts promise to open new doors to an ever-expanding range and diversity of renewable chemical and material products. This short review will highlight recent and notable achievements related for the microbial production of aromatic chemicals.

  6. Catalytic Conversion of Renewable Resources into Bulk and Fine Chemicals.

    PubMed

    de Vries, Johannes G

    2016-12-01

    Several strategies can be chosen to convert renewable resources into chemicals. In this account, I exemplify the route that starts with so-called platform chemicals; these are relatively simple chemicals that can be produced in high yield, directly from renewable resources, either via fermentation or via chemical routes. They can be converted into the existing bulk chemicals in a very efficient manner using multistep catalytic conversions. Two examples are given of the conversion of sugars into nylon intermediates. 5-Hydroxymethylfurfural (HMF) can be prepared in good yield from fructose. Two hydrogenation steps convert HMF into 1,6-hexanediol. Oppenauer oxidation converts this product into caprolactone, which in the past, has been converted into caprolactam in a large-scale industrial process by reaction with ammonia. An even more interesting platform chemical is levulinic acid (LA), which can be obtained directly from lignocellulose in good yield by treatment with dilute sulfuric acid at 200°C. Hydrogenation converts LA into gamma-valerolactone, which is ring-opened and esterified in a gas-phase process to a mixture of isomeric methyl pentenoates in excellent selectivity. In a remarkable selective palladium-catalysed isomerising methoxycarbonylation, this mixture is converted in to dimethyl adipate, which is finally hydrolysed to adipic acid. Overall selectivities of both processes are extremely high. The conversion of lignin into chemicals is a much more complicated task in view of the complex nature of lignin. It was discovered that breakage of the most prevalent β-O-4 bond in lignin occurs not only via the well-documented C3 pathway, but also via a C2 pathway, leading to the formation of highly reactive phenylacetaldehydes. These compounds went largely unnoticed as they immediately recondense on lignin. We have now found that it is possible to prevent this by converting these aldehydes in a tandem reaction, as they are formed. For this purpose, we have used

  7. Chemical nature of implant-derived titanium(IV) ions in synovial fluid

    SciTech Connect

    Silwood, Christopher J.L.; Grootveld, Martin . E-mail: grootvm@lsbu.ac.uk

    2005-05-13

    Previous investigations have indicated a deleterious leakage of Ti(III) and/or Ti(IV) species from Ti-Al-V alloy joint prostheses into adjacent tissue, synovium or synovial fluid (SF) in vivo. In view of the importance of the particular chemical nature of such complexes in determining their biological activity, we have employed high field proton ({sup 1}H) NMR spectroscopy to 'speciate' Ti(IV) in inflammatory SF. Treatment of osteoarthritic SF samples with increasing concentrations of Ti(IV) (0.10-1.03 mM [TiO(C{sub 2}O{sub 4}){sub 2}]{sup 2-}) gave rise to a specific broadening of the citrate proton resonances, indicating that this bioavailable oxygen-donor ligand plays an important role in complexing implant-derived Ti(IV). {sup 1}H NMR analysis of Ti(IV)-loaded SF samples subsequently treated with a large excess of ascorbate (0.05 M) showed that this added Ti(IV) chelator was only poorly effective in removing this metal ion from Ti(IV)-citrate/Ti(IV)-oxycitrate complexes. The results obtained here provide evidence for complexation of the low-molecular-mass (non-protein-bound) fraction of implant-derived Ti(IV) by citrate in vivo.

  8. Synthesis and Characterization of Tin(IV) Oxide Obtained by Chemical Vapor Deposition Method

    NASA Astrophysics Data System (ADS)

    Nagirnyak, Svitlana V.; Lutz, Victoriya A.; Dontsova, Tatiana A.; Astrelin, Igor M.

    2016-07-01

    The effect of precursors on the characteristics of tin oxide obtained by chemical vapor deposition (CVD) method was investigated. The synthesis of nanosized tin(IV) oxide was carried out with the use of two different precursors: tin(II) oxalate obtained using tin chloride(II) and oxalic acid; tin(II) oxalate obtained using tin chloride(II); and ammonium oxalate. The synthesized tin(IV) oxide samples were studied by electron microscopy, X-ray diffraction and optical spectra. The lattice parameters of tin(IV) oxide samples were defined, the bandgap of samples were calculated.

  9. Synthesis and Characterization of Tin(IV) Oxide Obtained by Chemical Vapor Deposition Method.

    PubMed

    Nagirnyak, Svitlana V; Lutz, Victoriya A; Dontsova, Tatiana A; Astrelin, Igor M

    2016-12-01

    The effect of precursors on the characteristics of tin oxide obtained by chemical vapor deposition (CVD) method was investigated. The synthesis of nanosized tin(IV) oxide was carried out with the use of two different precursors: tin(II) oxalate obtained using tin chloride(II) and oxalic acid; tin(II) oxalate obtained using tin chloride(II); and ammonium oxalate. The synthesized tin(IV) oxide samples were studied by electron microscopy, X-ray diffraction and optical spectra. The lattice parameters of tin(IV) oxide samples were defined, the bandgap of samples were calculated.

  10. Fluids in porous media. IV. Quench effect on chemical potential

    NASA Astrophysics Data System (ADS)

    Qiao, C. Z.; Zhao, S. L.; Liu, H. L.; Dong, W.

    2017-06-01

    It appears to be a common sense to measure the crowdedness of a fluid system by the densities of the species constituting it. In the present work, we show that this ceases to be valid for confined fluids under some conditions. A quite thorough investigation is made for a hard sphere (HS) fluid adsorbed in a hard sphere matrix (a quench-annealed system) and its corresponding equilibrium binary mixture. When fluid particles are larger than matrix particles, the quench-annealed system can appear much more crowded than its corresponding equilibrium binary mixture, i.e., having a much higher fluid chemical potential, even when the density of each species is strictly the same in both systems, respectively. We believe that the insight gained from this study should be useful for the design of functionalized porous materials.

  11. Synthesis of renewable fine-chemical building blocks by reductive coupling between furfural derivatives and terpenes.

    PubMed

    Nicklaus, Céline M; Minnaard, Adriaan J; Feringa, Ben L; de Vries, Johannes G

    2013-09-01

    Sugar and Spice…: The use of renewable resources to produce fine chemicals is an underdeveloped area. A waste-free technology will be necessary to further convert platform chemicals, readily available from biomass. We show that furfurals, which can be obtained from C5 sugars, can be coupled with terpenes in up to 95% yield through ruthenium-catalyzed reductive couplings developed by Krische et al.

  12. 77 FR 24988 - Manufacturer of Controlled Substances; Notice of Registration; ISP Freetown Fine Chemicals

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-04-26

    ..., verification of the company's compliance with state and local laws, and a review of the company's background... Amphetamine (1100) II Phenylacetone (8501) II The company plans to manufacture bulk API, for distribution to... ISP Freetown Fine Chemicals to ensure that the company's registration is consistent with the public...

  13. 78 FR 5500 - Manufacturer of Controlled Substances; Notice of Registration; Ampac Fine Chemicals, LLC

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-01-25

    ...; verification of the company's compliance with state and local laws; and a review of the company's background... II. The company plans to manufacture the listed controlled substance for distribution to its... AMPAC Fine Chemicals, LLC to ensure that the company's registration is consistent with the public...

  14. 77 FR 60145 - Manufacturer of Controlled Substances; Notice of Application; AMPAC Fine Chemicals, LLC

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-10-02

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Application; AMPAC Fine Chemicals..., California 95670, made application by letter to the Drug Enforcement Administration (DEA) to be registered...

  15. CHEMICAL ANALYSIS OF WORLD TRADE CENTER FINE PARTICULATE MATTER FOR USE IN TOXICOLOGICAL ASSESSMENT

    EPA Science Inventory

    Chemical Analysis of World Trade Center Fine Particulate Matter for Use in Toxicological Assessment
    John K. McGee1, Lung Chi Chen2, Mitchell D. Cohen2, Glen R. Chee2, Colette M. Prophete2, Najwa Haykal-Coates1, Shirley J. Wasson3, Teri L. Conner4, Daniel L. Costa1, and Steph...

  16. CHEMICAL ANALYSIS OF WORLD TRADE CENTER FINE PARTICULATE MATTER FOR USE IN TOXICOLOGICAL ASSESSMENT

    EPA Science Inventory

    Chemical Analysis of World Trade Center Fine Particulate Matter for Use in Toxicological Assessment
    John K. McGee1, Lung Chi Chen2, Mitchell D. Cohen2, Glen R. Chee2, Colette M. Prophete2, Najwa Haykal-Coates1, Shirley J. Wasson3, Teri L. Conner4, Daniel L. Costa1, and Steph...

  17. Fine-scale chemical exposure differs in point and nonpoint source plumes.

    PubMed

    Lahman, Sara E; Moore, Paul A

    2015-05-01

    Increasing influxes of anthropogenic chemicals into aquatic ecosystems has led to growing global concern surrounding human and ecosystem health. As more freshwater systems are deemed not potable or usable for agricultural purposes, more attention is being paid to remediation and mitigation efforts. Predicting and preventing the impacts of the chemical inputs first requires a thorough understanding of the spatio-temporal distribution of chemical plumes in natural habitats. Plume dispersion is intimately tied to fluid mechanics; therefore, alterations in the way that chemical plumes are introduced to habitats can have profound effects on chemical distribution. Such alterations can subsequently alter the exposure to which organisms are subjected. This study examined the influence of point versus nonpoint sources in structuring the distribution of chemicals in a simulated flowing freshwater habitat. The fine-scale (molecular) spatio-temporal distribution of chemicals was measured in situ using an electrochemical detector. Molecular concentration at varying distance and height from the source was quantified using dopamine coupled with an electrochemical detection system. The fine-scale distribution of chemical plumes from point and nonpoint sources showed significant differences in how organisms will be exposed to chemicals. Overall, this study characterized plumes from nonpoint sources as having significantly longer peak lengths and rise times as well as greater peak heights and maximum slopes than plumes from point sources, thus providing a significantly different exposure paradigm. This quantification of how chemicals move differently throughout a fluid medium when introduced from point and nonpoint sources allows a greater understanding of how chemical plumes can potentially affect aquatic ecosystems.

  18. Chemical treatment of plutonium with hydrogen peroxide before nitrate anion exchange processing. [Reduction to (IV)

    SciTech Connect

    Marsh, S.F.; Gallegos, T.D.

    1987-05-01

    The major aqueous process used to recover and purify plutonium at the Los Alamos Plutonium Facility is anion exchange in nitric acid. This process is highly selective for plutonium; however, all plutonium must be as Pu(IV) to form the strongly sorbed anionic nitrato complex. The previous ''full-reduction treatment'' used at Los Alamos to obtain Pu(IV) results in a three- to fourfold increase in the feed solution volume and the introduction of kilogram quantities of extraneous salts immediately before a process whose function is to remove such impurities. That treatment has been successfully replaced by a single reagent, hydrogen peroxide, which converts all plutonium to Pu(IV), minimally increases the feed volume, and introduces no residual impurities. Safety aspects of this revised chemical treatment are addressed.

  19. Determination of Stoichiometry in Lanthanum Strontium Manganates(III)(IV) by Wet Chemical Methods

    NASA Astrophysics Data System (ADS)

    Andersen, I. G. Krogh; Andersen, E. Krogh; Norby, P.; Skou, E.

    1994-12-01

    Wet chemical analyses and powder diffractometry were used to characterize lanthanum strontium manganates(III)(IV) with a composition La1-xSrxMnO3+δ (0.00 ≤ x ≤ 0.50). Two series prepared by different thermal treatments were investigated. In series I the materials were calcined in air. These materials were hexagonal. In series II the materials were prepared from series I materials by calcination in a nitrogen atmosphere. Series II materials with 0.00 ≤ x < 0.20 were orthorhombic. For x ≥ 0.20, series II materials were hexagonal. For series I δ decreases with increasing x until x = 0.30, where it becomes almost zero (and remains 0 for x > 0.30. For series I the molar ratio Mn(IV)/Mn(IV) + Mn(III) is a nearly constant 0.3 in the range 0.00 ≤ x ≤ 0.20. For series II δ is near zero in the whole range. For these materials the ratio Mn(IV)/Mn(IV) + Mn(III) increases with x. The changes of unit cell volumes with x is shown to be consistent with the found composition of the materials. The observed and calculated densities of the materials are consistent with cation vacancies. Full descriptions of procedures for syntheses and analyses are reported.

  20. Impact of synthetic biology and metabolic engineering on industrial production of fine chemicals.

    PubMed

    Jullesson, David; David, Florian; Pfleger, Brian; Nielsen, Jens

    2015-11-15

    Industrial bio-processes for fine chemical production are increasingly relying on cell factories developed through metabolic engineering and synthetic biology. The use of high throughput techniques and automation for the design of cell factories, and especially platform strains, has played an important role in the transition from laboratory research to industrial production. Model organisms such as Saccharomyces cerevisiae and Escherichia coli remain widely used host strains for industrial production due to their robust and desirable traits. This review describes some of the bio-based fine chemicals that have reached the market, key metabolic engineering tools that have allowed this to happen and some of the companies that are currently utilizing these technologies for developing industrial production processes.

  1. Stark broadening of Zr IV spectral lines in the atmospheres of chemically peculiar stars

    NASA Astrophysics Data System (ADS)

    Majlinger, Zlatko; Simić, Zoran; Dimitrijević, Milan S.

    2017-09-01

    Stark widths for 18 Zr IV spectral lines have been calculated by using the modified semi-empirical method. The obtained results have been used to investigate the influence of Stark broadening on the spectra of atmospheres of chemically peculiar stars of A spectral type and hydrogen-rich DA and helium-rich DB white dwarfs. Our results have been used also to test possibility to predict new data using some approximate methods developed on the basis on regularities and systematic trends.

  2. Chemical input and I-V output: stepwise chemical information processing in dye-sensitized solar cells.

    PubMed

    Satoh, Norifusa; Han, Liyuan

    2012-12-14

    As a complex system, a dye-sensitized solar cell (DSC) exhibits emergent photovoltaics not obvious from the properties of the individual components. The chemical input of 4-tert-butylpyridine (TBP) into DSC improves the open circuit voltage (V(oc)) and reduces the short circuit current (I(sc)) in I-V output through multiple interactions with the components, yet it has been difficult to distinguish the multiple interactions and correlate the interactions with the influences on I-V output due to the complexity of the system. To deal with the multiple interactions, we have adapted a conceptual framework and methodology from coordination chemistry. First, we titrated the photovoltaic interface and electrolyte with TBP to identify the stepwise chemical interaction processes. An isopotential point observed in I-V output indicates that most of the inputted chemicals interact with the electrolyte. Cyclic voltammetric titration of the electrolyte demonstrates asymmetric redox peaks and two different isopotential points, indicating that the two-step coordination-decoordination process inhibits the reduction current of the electrolyte. Second, we set an interaction model bridging the hierarchical gaps between the multiple interactions and the I-V output to address the influences on outputs from the amount of the inputs. From the viewpoint of the interaction model and interactions observed, we are able to comprehend the processes of the complex system and suggest a direction to improve V(oc) without sacrificing I(sc) in DSCs. We conclude that the conceptual framework and methodology adapted from coordination chemistry is beneficial to enhance the emergent outputs of complex systems.

  3. Impact of chemical leaching on permeability and cadmium removal from fine-grained soils.

    PubMed

    Lin, Zhongbing; Zhang, Renduo; Huang, Shuang; Wang, Kang

    2017-06-21

    The aim of this study was to investigate the influence of chemical leaching on permeability and Cd removal from fine-grained polluted soils. Column leaching experiments were conducted using two types of soils (i.e., artificially Cd-polluted loam and historically polluted silty loam). Chemical agents of CaCl2, FeCl3, citric acid, EDTA, rhamnolipid, and deionized water were used to leach Cd from the soils. Results showed that organic agents reduced permeability of both soils, and FeCl3 reduced permeability of loam soil, compared with inorganic agents and deionized water. Entrapment and deposition of colloids generated from the organic agents and FeCl3 treatments reduced the soil permeability. The peak Cd effluence from the artificially polluted loam columns was retarded. For the artificially polluted soils treated with EDTA and the historically polluted soils with FeCl3, Cd precipitates were observed at the bottom after chemical leaching. When Cd was associated with large colloid particles, the reduction of soil permeability caused Cd accumulation in deeper soil. In addition, the slow process of disintegration of soil clay during chemical leaching might result in the retardation of peak Cd effluence. These results suggest the need for caution when using chemical-leaching agents for Cd removal in fine-grained soils.

  4. Chemical speciation and source apportionment of fine particulate matter in Santiago, Chile, 2013.

    PubMed

    Villalobos, Ana M; Barraza, Francisco; Jorquera, Héctor; Schauer, James J

    2015-04-15

    Santiago is one of the largest cities in South America and has experienced high fine particulate matter (PM2.5) concentrations in fall and winter months for decades. To better understand the sources of fall and wintertime pollution in Santiago, PM2.5 samples were collected for 24 h every weekday from March to October 2013 for chemical analysis. Samples were analyzed for mass, elemental carbon (EC), organic carbon (OC), water soluble organic carbon (WSOC), water soluble nitrogen (WSTN), secondary inorganic ions, and particle-phase organic tracers for source apportionment. Selected samples were analyzed as monthly composites for organic tracers. PM2.5 concentrations were considerably higher in the coldest months (June-July), averaging (mean ± standard deviation) 62±15 μg/m(3) in these two months. Average fine particle mass concentration during the study period was 40±20 μg/m(3). Organic matter during the peak winter months was the major component of fine particles comprising around 70% of the particle mass. Source contributions to OC were calculated using organic molecular markers and a chemical mass balance (CMB) receptor model. The four combustion sources identified were wood smoke, diesel engine emission, gasoline vehicles, and natural gas. Wood smoke was the predominant source of OC, accounting for 58±42% of OC in fall and winter. Wood smoke and nitrate were the major contributors to PM2.5. In fall and winter, wood smoke accounted for 9.8±7.1 μg/m(3) (21±15%) and nitrate accounted for 9.1±4.8 μg/m(3) (20±10%) of fine PM. The sum of secondary inorganic ions (sulfate, nitrate, and ammonium) represented about 30% of PM2.5 mass. Secondary organic aerosols contributed only in warm months, accounting for about 30% of fine PM during this time. Copyright © 2015 Elsevier B.V. All rights reserved.

  5. Spontaneous fine-tuning to environment in many-species chemical reaction networks

    NASA Astrophysics Data System (ADS)

    Horowitz, Jordan M.; England, Jeremy L.

    2017-07-01

    A chemical mixture that continually absorbs work from its environment may exhibit steady-state chemical concentrations that deviate from their equilibrium values. Such behavior is particularly interesting in a scenario where the environmental work sources are relatively difficult to access, so that only the proper orchestration of many distinct catalytic actors can power the dissipative flux required to maintain a stable, far-from-equilibrium steady state. In this article, we study the dynamics of an in silico chemical network with random connectivity in an environment that makes strong thermodynamic forcing available only to rare combinations of chemical concentrations. We find that the long-time dynamics of such systems are biased toward states that exhibit a fine-tuned extremization of environmental forcing.

  6. Spontaneous fine-tuning to environment in many-species chemical reaction networks.

    PubMed

    Horowitz, Jordan M; England, Jeremy L

    2017-07-18

    A chemical mixture that continually absorbs work from its environment may exhibit steady-state chemical concentrations that deviate from their equilibrium values. Such behavior is particularly interesting in a scenario where the environmental work sources are relatively difficult to access, so that only the proper orchestration of many distinct catalytic actors can power the dissipative flux required to maintain a stable, far-from-equilibrium steady state. In this article, we study the dynamics of an in silico chemical network with random connectivity in an environment that makes strong thermodynamic forcing available only to rare combinations of chemical concentrations. We find that the long-time dynamics of such systems are biased toward states that exhibit a fine-tuned extremization of environmental forcing.

  7. Nitridation of fine grain chemical vapor deposited tungsten film as diffusion barrier for aluminum metallization

    NASA Astrophysics Data System (ADS)

    Chang, Kow-Ming; Yeh, Ta-Hsun; Deng, I.-Chung

    1997-04-01

    A novel tungsten nitride (WNx) film for diffusion barrier applications has been prepared by nitridation of a fine grain chemical vapor deposited tungsten (CVD-W) film. The fine grain CVD-W is deposited at 300 °C in a low pressure chemical vapor deposition reactor with a SiH4/WF6 flow rate of 12.5/5 sccm under a total gas pressure of 100 mTorr. The subsequent nitridation process is executed in nitrogen plasma at 300 °C without breaking vacuum. The thickness of WNx layer as examined by secondary ion mass spectroscopy is 50 nm after 5 min exposure to nitrogen plasma. X-ray photoelectron spectroscopy spectra shows that the atomic ratio of tungsten to nitrogen in WNx layer is 2:1. According to the analysis by Auger electron spectroscopy and the measurement of n+p junction leakage current, the Al/WNx/W/Si multilayer maintains excellent interfacial stability after furnace annealing at 575 °C for 30 min. The effectiveness of W2N barrier is attributed to stuffing grain boundaries with nitrogen atoms which eliminates the rapid diffusion paths in fine grain CVD-W films.

  8. Nitridation of fine grain chemical vapor deposited tungsten film as diffusion barrier for aluminum metallization

    SciTech Connect

    Chang, K.; Yeh, T.; Deng, I.

    1997-04-01

    A novel tungsten nitride (WN{sub x}) film for diffusion barrier applications has been prepared by nitridation of a fine grain chemical vapor deposited tungsten (CVD-W) film. The fine grain CVD-W is deposited at 300{degree}C in a low pressure chemical vapor deposition reactor with a SiH{sub 4}/WF{sub 6} flow rate of 12.5/5 sccm under a total gas pressure of 100 mTorr. The subsequent nitridation process is executed in nitrogen plasma at 300{degree}C without breaking vacuum. The thickness of WN{sub x} layer as examined by secondary ion mass spectroscopy is 50 nm after 5 min exposure to nitrogen plasma. X-ray photoelectron spectroscopy spectra shows that the atomic ratio of tungsten to nitrogen in WN{sub x} layer is 2:1. According to the analysis by Auger electron spectroscopy and the measurement of n{sup +}p junction leakage current, the Al/WN{sub x}/W/Si multilayer maintains excellent interfacial stability after furnace annealing at 575{degree}C for 30 min. The effectiveness of W{sub 2}N barrier is attributed to stuffing grain boundaries with nitrogen atoms which eliminates the rapid diffusion paths in fine grain CVD-W films. {copyright} {ital 1997 American Institute of Physics.}

  9. Mercury transformations in chemical agent simulant as characterized by X-ray absorption fine spectroscopy.

    PubMed

    Skubal, Laura R; Biedron, Sandra G; Newville, Matthew; Schneider, John F; Milton, Stephen V; Pianetta, Piero; O'Neill, H Jack

    2005-10-15

    Chemical analyses of U.S. stockpiled mustard chemical warfare agent show some agent destined for destruction contains mercury [L. Ember, Chem. Eng. News 82 (2004) 8]. Because of its toxicity, mercury must be removed from agent prior to incineration or be scrubbed from incineration exhaust to prevent release into the atmosphere. Understanding mercury/agent interactions is critical if either atmospheric or aqueous treatment processes are used. We investigate and compare the state of mercury in water to that in thiodiglycol, a mustard simulant, as co-contaminants are introduced. The effects of sodium hypochlorite and sodium hydroxide, common neutralization chemicals, on mercury in water and simulant with and without co-contaminants present are examined using X-ray absorption fine spectroscopy (XAFS).

  10. Nonlinear dendritic integration of electrical and chemical synaptic inputs drives fine-scale correlations

    PubMed Central

    Trenholm, Stuart; McLaughlin, Amanda J; Schwab, David J; Turner, Maxwell H; Smith, Robert G; Rieke, Fred; Awatramani, Gautam B

    2014-01-01

    Throughout the CNS, gap junction–mediated electrical signals synchronize neural activity on millisecond timescales via cooperative interactions with chemical synapses. However, gap junction–mediated synchrony has rarely been studied in the context of varying spatiotemporal patterns of electrical and chemical synaptic activity. Thus, the mechanism underlying fine-scale synchrony and its relationship to neural coding remain unclear. We examined spike synchrony in pairs of genetically identified, electrically coupled ganglion cells in mouse retina. We found that coincident electrical and chemical synaptic inputs, but not electrical inputs alone, elicited synchronized dendritic spikes in subregions of coupled dendritic trees. The resulting nonlinear integration produced fine-scale synchrony in the cells’ spike output, specifically for light stimuli driving input to the regions of dendritic overlap. In addition, the strength of synchrony varied inversely with spike rate. Together, these features may allow synchronized activity to encode information about the spatial distribution of light that is ambiguous on the basis of spike rate alone. PMID:25344631

  11. X-Band Electron Paramagnetic Resonance Comparison of Mononuclear Mn(IV)-oxo and Mn(IV)-hydroxo Complexes and Quantum Chemical Investigation of Mn(IV) Zero-Field Splitting.

    PubMed

    Leto, Domenick F; Massie, Allyssa A; Colmer, Hannah E; Jackson, Timothy A

    2016-04-04

    X-band electron paramagnetic resonance (EPR) spectroscopy was used to probe the ground-state electronic structures of mononuclear Mn(IV) complexes [Mn(IV)(OH)2(Me2EBC)](2+) and [Mn(IV)(O)(OH)(Me2EBC)](+). These compounds are known to effect C-H bond oxidation reactions by a hydrogen-atom transfer mechanism. They provide an ideal system for comparing Mn(IV)-hydroxo versus Mn(IV)-oxo motifs, as they differ by only a proton. Simulations of 5 K EPR data, along with analysis of variable-temperature EPR signal intensities, allowed for the estimation of ground-state zero-field splitting (ZFS) and (55)Mn hyperfine parameters for both complexes. From this analysis, it was concluded that the Mn(IV)-oxo complex [Mn(IV)(O)(OH)(Me2EBC)](+) has an axial ZFS parameter D (D = +1.2(0.4) cm(-1)) and rhombicity (E/D = 0.22(1)) perturbed relative to the Mn(IV)-hydroxo analogue [Mn(IV)(OH)2(Me2EBC)](2+) (|D| = 0.75(0.25) cm(-1); E/D = 0.15(2)), although the complexes have similar (55)Mn values (a = 7.7 and 7.5 mT, respectively). The ZFS parameters for [Mn(IV)(OH)2(Me2EBC)](2+) were compared with values obtained previously through variable-temperature, variable-field magnetic circular dichroism (VTVH MCD) experiments. While the VTVH MCD analysis can provide a reasonable estimate of the magnitude of D, the E/D values were poorly defined. Using the ZFS parameters reported for these complexes and five other mononuclear Mn(IV) complexes, we employed coupled-perturbed density functional theory (CP-DFT) and complete active space self-consistent field (CASSCF) calculations with second-order n-electron valence-state perturbation theory (NEVPT2) correction, to compare the ability of these two quantum chemical methods for reproducing experimental ZFS parameters for Mn(IV) centers. The CP-DFT approach was found to provide reasonably acceptable values for D, whereas the CASSCF/NEVPT2 method fared worse, considerably overestimating the magnitude of D in several cases. Both methods were poor in

  12. Applying the Fe(III) binding property of a chemical transferrin mimetic to Ti(IV) anticancer drug design.

    PubMed

    Parks, Timothy B; Cruz, Yahaira M; Tinoco, Arthur D

    2014-02-03

    As an endogenous serum protein binder of Ti(IV), transferrin (Tf) serves as an excellent vehicle to stabilize the hydrolysis prone metal ion and successfully transport it into cells. This transporting role is thought to be central to Ti(IV)'s anticancer function, but efforts to synthesize Ti(IV) compounds targeting transferrin have not produced a drug. Nonetheless, the Ti(IV) transferrin complex (Ti2Tf) greatly informs on a new Ti(IV)-based anticancer drug design strategy. Ti2Tf interferes with cellular uptake of Fe(III), which is particularly detrimental to cancer cells because of their higher requirement for iron. Ti(IV) compounds of chemical transferrin mimetic (cTfm) ligands were designed to facilitate Ti(IV) activity by attenuating Fe(III) intracellular levels. In having a higher affinity for Fe(III) than Ti(IV), these ligands feature the appropriate balance between stability and lability to effectively transport Ti(IV) into cancer cells, release Ti(IV) via displacement by Fe(III), and deplete the intracellular Fe(III) levels. The cTfm ligand N,N'-di(o-hydroxybenzyl)ethylenediamine-N,N'-diacetic acid (HBED) was selected to explore the feasibility of the design strategy. Kinetic studies on the Fe(III) displacement process revealed that Ti(IV) can be transported and released into cells by HBED on a physiologically relevant time scale. Cell viability studies using A549 cancerous and MRC5 normal human lung cells and testing the cytotoxicity of HBED and its Ti(IV), Fe(III), and Ga(III) compounds demonstrate the importance of Fe(III) depletion in the proposed drug design strategy and the specificity of the strategy for Ti(IV) activity. The readily derivatized cTfm ligands demonstrate great promise for improved Ti(IV) anticancer drugs.

  13. Seasonal trends, chemical speciation and source apportionment of fine PM in Tehran

    NASA Astrophysics Data System (ADS)

    Arhami, Mohammad; Hosseini, Vahid; Zare Shahne, Maryam; Bigdeli, Mostafa; Lai, Alexandra; Schauer, James J.

    2017-03-01

    Frequent air pollution episodes have been reported for Tehran, Iran, mainly because of critically high levels of fine particulate matter (PM2.5). The composition and sources of these particles are poorly known, so this study aims to identify the major components and heavy metals in PM2.5 along with their seasonal trends and associated sources. 24-hour PM2.5 samples were collected at a main residential station every 6 days for a full year from February 2014 to February 2015. The samples were analyzed for ions, organic carbon (including water-soluble and insoluble portions), elemental carbon (EC), and all detectable elements. The dominant mass components, which were determined by means of chemical mass closure, were organic matter (35%), dust (25%), non-sea salt sulfate (11%), EC (9%), ammonium (5%), and nitrate (2%). Organic matter and EC together comprised 44% of fine PM on average (increased to >70% in the colder season), which reflects the significance of anthropogenic urban sources (i.e. vehicles). The contributions of different components varied considerably throughout the year, particularly the dust component that varied from 7% in the cold season to 56% in the hot and dry season. Principal component analyses were applied, resulting in 5 major source factors that explained 85% of the variance in fine PM. Factor 1, representing soil dust, explained 53%; Factor 2 denotes heavy metals mainly found in industrial sources and accounted for 18%; and rest of factors, mainly representing combustion sources, explained 14% of the variation. The levels of major heavy metals were further evaluated, and their trends showed considerable increases during cold seasons. The results of this study provide useful insight to fine PM in Tehran, which could help in identifying their health effects and sources, and also adopting effective control strategies.

  14. Metabolism of fluoroorganic compounds in microorganisms: impacts for the environment and the production of fine chemicals.

    PubMed

    Murphy, Cormac D; Clark, Benjamin R; Amadio, Jessica

    2009-09-01

    Incorporation of fluorine into an organic compound can favourably alter its physicochemical properties with respect to biological activity, stability and lipophilicity. Accordingly, this element is found in many pharmaceutical and industrial chemicals. Organofluorine compounds are accepted as substrates by many enzymes, and the interactions of microorganisms with these compounds are of relevance to the environment and the fine chemicals industry. On the one hand, the microbial transformation of organofluorines can lead to the generation of toxic compounds that are of environmental concern, yet similar biotransformations can yield difficult-to-synthesise products and intermediates, in particular derivatives of biologically active secondary metabolites. In this paper, we review the historical and recent developments of organofluorine biotransformation in microorganisms and highlight the possibility of using microbes as models of fluorinated drug metabolism in mammals.

  15. Tailor-made biocatalysts enzymes for the fine chemical industry in China.

    PubMed

    Jiang, Yu; Tao, Rongsheng; Yang, Sheng

    2016-09-01

    The Center of Industrial Biotechnology (CIBT) was established in Huzhou for fine chemicals in 2006 and CIBT Shanghai was founded for bulk chemicals in 2008. CIBT is a non-profit organization under auspices of the Shanghai Institutes for Biological Sciences, Shanghai Branch of the Chinese Academy of Sciences (CAS) and Huzhou Municipal Government. CIBT is affiliated with the CAS, which enables it to take advantage of the rich R&D resources and support from CAS; yet CIBT operates as an independent legal entity. The goal of CIBT is to incubate industrial biotechnologies and accelerate the commercialization of these technologies with corporate partners in China. Copyright © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Chromium Extraction via Chemical Processing of Fe-Cr Alloys Fine Powder with High Carbon Content

    NASA Astrophysics Data System (ADS)

    Torres, D. M.; Navarro, R. C. S.; Souza, R. F. M.; Brocchi, E. A.

    2017-03-01

    Ferrous alloys are important raw materials for special steel production. In this context, alloys from the Fe-Cr system, with typical Cr weight fraction ranging from 0.45 to 0.95, are prominent, particularly for the stainless steel industry. During the process in which these alloys are obtained, there is considerable production of fine powder, which could be reused after suitable chemical treatment, for example, through coupling pyrometallurgical and hydrometallurgical processes. In the present study, the extraction of chromium from fine powder generated during the production of a Fe-Cr alloy with high C content was investigated. Roasting reactions were performed at 1073 K, 1173 K, and 1273 K (800 °C, 900 °C, and 1000 °C) with 300 pct (w/w) excess NaOH in an oxidizing atmosphere (air), followed by solubilization in deionized water, selective precipitation, and subsequent calcination at 1173 K (900 °C) in order to convert the obtained chromium hydroxide to Cr2O3. The maximum achieved Cr recovery was around 86 pct, suggesting that the proposed chemical route was satisfactory regarding the extraction of the chromium initially present. Moreover, after X-ray diffraction analysis, the final produced oxide has proven to be pure Cr2O3 with a mean crystallite size of 200 nm.

  17. Chromium Extraction via Chemical Processing of Fe-Cr Alloys Fine Powder with High Carbon Content

    NASA Astrophysics Data System (ADS)

    Torres, D. M.; Navarro, R. C. S.; Souza, R. F. M.; Brocchi, E. A.

    2017-06-01

    Ferrous alloys are important raw materials for special steel production. In this context, alloys from the Fe-Cr system, with typical Cr weight fraction ranging from 0.45 to 0.95, are prominent, particularly for the stainless steel industry. During the process in which these alloys are obtained, there is considerable production of fine powder, which could be reused after suitable chemical treatment, for example, through coupling pyrometallurgical and hydrometallurgical processes. In the present study, the extraction of chromium from fine powder generated during the production of a Fe-Cr alloy with high C content was investigated. Roasting reactions were performed at 1073 K, 1173 K, and 1273 K (800 °C, 900 °C, and 1000 °C) with 300 pct (w/w) excess NaOH in an oxidizing atmosphere (air), followed by solubilization in deionized water, selective precipitation, and subsequent calcination at 1173 K (900 °C) in order to convert the obtained chromium hydroxide to Cr2O3. The maximum achieved Cr recovery was around 86 pct, suggesting that the proposed chemical route was satisfactory regarding the extraction of the chromium initially present. Moreover, after X-ray diffraction analysis, the final produced oxide has proven to be pure Cr2O3 with a mean crystallite size of 200 nm.

  18. Characterization of Fine Particulate Matter and Associations between Particulate Chemical Constituents and Mortality in Seoul, Korea

    PubMed Central

    Son, Ji-Young; Lee, Jong-Tae; Kim, Ki-Hyun; Jung, Kweon

    2012-01-01

    Background: Numerous studies have linked fine particles [≤ 2.5 µm in aerodynamic diameter (PM2.5)] and health. Most studies focused on the total mass of the particles, although the chemical composition of the particles varies substantially. Which chemical components of fine particles that are the most harmful is not well understood, and research on the chemical composition of PM2.5 and the components that are the most harmful is particularly limited in Asia. Objectives: We characterized PM2.5 chemical composition and estimated the effects of cause-specific mortality of PM2.5 mass and constituents in Seoul, Korea. We compared the chemical composition of particles to those of the eastern and western United States. Methods: We examined temporal variability of PM2.5 mass and its composition using hourly data. We applied an overdispersed Poisson generalized linear model, adjusting for time, day of week, temperature, and relative humidity to investigate the association between risk of mortality and PM2.5 mass and its constituents in Seoul, Korea, for August 2008 through October 2009. Results: PM2.5 and chemical components exhibited temporal patterns by time of day and season. The chemical characteristics of Seoul’s PM2.5 were more similar to PM2.5 found in the western United States than in the eastern United States. Seoul’s PM2.5 had lower sulfate (SO4) contributions and higher nitrate (NO3) contributions than that of the eastern United States, although overall PM2.5 levels in Seoul were higher than in the United States. An interquartile range (IQR) increase in magnesium (Mg) (0.05 μg/m3) was associated with a 1.4% increase (95% confidence interval: 0.2%, 2.6%) in total mortality on the following day. Several components that were among the largest contributors to PM2.5 total mass—NO3, SO4, and ammonium (NH4)—were moderately associated with same-day cardiovascular mortality at the p < 0.10 level. Other components with smaller mass contributions [Mg and

  19. Global Chemical Composition of Ambient Fine Particulate Matter for Exposure Assessment

    DOE PAGES

    Philip, Sajeev; Martin, Randall V.; van Donkelaar, Aaron; ...

    2014-10-24

    Epidemiologic and health impact studies are inhibited by the paucity of global, long-term measurements of the chemical composition of fine particulate matter. We inferred PM2.5 chemical composition at 0.1° × 0.1° spatial resolution for 2004–2008 by combining aerosol optical depth retrieved from the MODIS and MISR satellite instruments, with coincident profile and composition information from the GEOS-Chem global chemical transport model. Evaluation of the satellite-model PM2.5 composition data set with North American in situ measurements indicated significant spatial agreement for secondary inorganic aerosol, particulate organic mass, black carbon, mineral dust, and sea salt. We found that global population-weighted PM2.5 concentrationsmore » were dominated by particulate organic mass (11.9 ± 7.3 μg/m3), secondary inorganic aerosol (11.1 ± 5.0 μg/m3), and mineral dust (11.1 ± 7.9 μg/m3). Secondary inorganic PM2.5 concentrations exceeded 30 μg/m3 over East China. Sensitivity simulations suggested that population-weighted ambient PM2.5 from biofuel burning (11 μg/m3) could be almost as large as from fossil fuel combustion sources (17 μg/m3). In conclusion, these estimates offer information about global population exposure to the chemical components and sources of PM2.5.« less

  20. Global Chemical Composition of Ambient Fine Particulate Matter for Exposure Assessment

    PubMed Central

    2015-01-01

    Epidemiologic and health impact studies are inhibited by the paucity of global, long-term measurements of the chemical composition of fine particulate matter. We inferred PM2.5 chemical composition at 0.1° × 0.1° spatial resolution for 2004–2008 by combining aerosol optical depth retrieved from the MODIS and MISR satellite instruments, with coincident profile and composition information from the GEOS-Chem global chemical transport model. Evaluation of the satellite-model PM2.5 composition data set with North American in situ measurements indicated significant spatial agreement for secondary inorganic aerosol, particulate organic mass, black carbon, mineral dust, and sea salt. We found that global population-weighted PM2.5 concentrations were dominated by particulate organic mass (11.9 ± 7.3 μg/m3), secondary inorganic aerosol (11.1 ± 5.0 μg/m3), and mineral dust (11.1 ± 7.9 μg/m3). Secondary inorganic PM2.5 concentrations exceeded 30 μg/m3 over East China. Sensitivity simulations suggested that population-weighted ambient PM2.5 from biofuel burning (11 μg/m3) could be almost as large as from fossil fuel combustion sources (17 μg/m3). These estimates offer information about global population exposure to the chemical components and sources of PM2.5. PMID:25343705

  1. Mapping the patent landscape of synthetic biology for fine chemical production pathways.

    PubMed

    Carbonell, Pablo; Gök, Abdullah; Shapira, Philip; Faulon, Jean-Loup

    2016-09-01

    A goal of synthetic biology bio-foundries is to innovate through an iterative design/build/test/learn pipeline. In assessing the value of new chemical production routes, the intellectual property (IP) novelty of the pathway is important. Exploratory studies can be carried using knowledge of the patent/IP landscape for synthetic biology and metabolic engineering. In this paper, we perform an assessment of pathways as potential targets for chemical production across the full catalogue of reachable chemicals in the extended metabolic space of chassis organisms, as computed by the retrosynthesis-based algorithm RetroPath. Our database for reactions processed by sequences in heterologous pathways was screened against the PatSeq database, a comprehensive collection of more than 150M sequences present in patent grants and applications. We also examine related patent families using Derwent Innovations. This large-scale computational study provides useful insights into the IP landscape of synthetic biology for fine and specialty chemicals production. © 2016 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology.

  2. SYNBIOCHEM–a SynBio foundry for the biosynthesis and sustainable production of fine and speciality chemicals

    PubMed Central

    Carbonell, Pablo; Currin, Andrew; Dunstan, Mark; Fellows, Donal; Jervis, Adrian; Rattray, Nicholas J.W.; Robinson, Christopher J.; Swainston, Neil; Vinaixa, Maria; Williams, Alan; Yan, Cunyu; Barran, Perdita; Breitling, Rainer; Chen, George Guo-Qiang; Faulon, Jean-Loup; Goble, Carole; Goodacre, Royston; Kell, Douglas B.; Feuvre, Rosalind Le; Micklefield, Jason; Scrutton, Nigel S.; Shapira, Philip; Takano, Eriko; Turner, Nicholas J.

    2016-01-01

    The Manchester Synthetic Biology Research Centre (SYNBIOCHEM) is a foundry for the biosynthesis and sustainable production of fine and speciality chemicals. The Centre's integrated technology platforms provide a unique capability to facilitate predictable engineering of microbial bio-factories for chemicals production. An overview of these capabilities is described. PMID:27284023

  3. SYNBIOCHEM-a SynBio foundry for the biosynthesis and sustainable production of fine and speciality chemicals.

    PubMed

    Carbonell, Pablo; Currin, Andrew; Dunstan, Mark; Fellows, Donal; Jervis, Adrian; Rattray, Nicholas J W; Robinson, Christopher J; Swainston, Neil; Vinaixa, Maria; Williams, Alan; Yan, Cunyu; Barran, Perdita; Breitling, Rainer; Chen, George Guo-Qiang; Faulon, Jean-Loup; Goble, Carole; Goodacre, Royston; Kell, Douglas B; Feuvre, Rosalind Le; Micklefield, Jason; Scrutton, Nigel S; Shapira, Philip; Takano, Eriko; Turner, Nicholas J

    2016-06-15

    The Manchester Synthetic Biology Research Centre (SYNBIOCHEM) is a foundry for the biosynthesis and sustainable production of fine and speciality chemicals. The Centre's integrated technology platforms provide a unique capability to facilitate predictable engineering of microbial bio-factories for chemicals production. An overview of these capabilities is described.

  4. EFFECTS OF CHEMICAL DISPERSANTS AND MINERAL FINES ON CRUDE OIL DISPERSION IN A WAVE TANK UNDER BREAKING WAVES

    EPA Science Inventory

    The interaction of chemical dispersants and suspended sediments with crude oil influences the fate and transport of oil spills in coastal waters. A wave tank study was conducted to investigate the effects of chemical dispersants and mineral fines on the dispersion of oil and the ...

  5. EFFECTS OF CHEMICAL DISPERSANTS AND MINERAL FINES ON CRUDE OIL DISPERSION IN A WAVE TANK UNDER BREAKING WAVES

    EPA Science Inventory

    The interaction of chemical dispersants and suspended sediments with crude oil influences the fate and transport of oil spills in coastal waters. A wave tank study was conducted to investigate the effects of chemical dispersants and mineral fines on the dispersion of oil and the ...

  6. Uranium(IV) oxidation during anoxic chemical extractions of natural sediment: Importance of Fe(III)

    NASA Astrophysics Data System (ADS)

    Campbell, K. M.; Davis, J. A.; Fuller, C. C.

    2008-12-01

    In situ reduction of soluble U(VI) to insoluble U(IV) precipitates is one promising solution for the remediation of U-contaminated aquifers. U(VI) reduction can occur upon stimulation of the native microbial community by injection of an electron donor or by the presence of natural organic matter. Contamination from a former U mill tailings repository (Rifle, CO) provides a research site to study the effects of in situ and natural bioreduction. An accurate method for determining solid-phase U oxidation state in sediments with elevated amounts of Fe and organic matter is necessary to evaluate the extent of bioreduction. The oxidation state of U in anaerobic sediment is often measured by a two-step bicarbonate/carbonate chemical extraction when spectroscopic methods are infeasible. In this study, anaerobic sediment samples from Rifle were analyzed for labile U(VI) content by extraction in anoxic conditions (pH 9.4, 14mM NaHCO3, 2.8 mM Na2CO3). A subset of each sediment sample was oxidized by exposure to air for 2 weeks. The extraction was repeated in air, and the amount of U(IV) present in the anaerobic sample was calculated by difference between the anoxic and oxidized extractions. For comparison, the U oxidation state was measured in several preserved samples by collecting X-ray absorption spectra (XANES). The XANES measurement indicated that approximately 90% was present as U(IV) prior to the extraction. In contrast, the extractions suggested evidence of substantial oxidation (<5% as U(IV)) even in an anoxic extraction. This discrepancy was eliminated when the anoxic extractions were repeated at pH 12, suggesting that Fe(III) may be an important oxidant for reduced U species during an anoxic extraction at pH 9.4, since the thermodynamic driving force for this reaction decreases at high pH. The results of an investigation of biogenic uraninite (UO2) oxidation by ferrihydrite in the pH range 7-12 under bicarbonate/carbonate extraction concentrations will be presented

  7. Fine-structure resolved photoionization of metastable Be-like ionsC III, N IV, and O V

    SciTech Connect

    Muller, A.; Schippers, S.; Phaneuf, R.A.; Kilcoyne, A.L.D.; Brauning, H.; Schlachter, A.S.; McLaughlin, B.M.

    2006-09-01

    High-resolution photoionization experiments were carried outwith beams of C III, N IV, and O V containing roughly equal amounts ofground-state and metastable ions. The energy scales of the experimentsare calibrated with uncertainties of 1 to 10 meV depending on photonenergy. These data favorably compare with state-of-the-art R-matrixcalculations carried out on an energy grid with a spacing of 13.6 mueV.

  8. Chemical characteristics of fine particles emitted from different gas cooking methods

    NASA Astrophysics Data System (ADS)

    See, Siao Wei; Balasubramanian, Rajasekhar

    Gas cooking is an important indoor source of fine particles (PM 2.5). The chemical characteristics of PM 2.5 emitted from different cooking methods, namely, steaming, boiling, stir-frying, pan-frying and deep-frying were investigated in a domestic kitchen. Controlled experiments were conducted to measure the mass concentration of PM 2.5 and its chemical constituents (elemental carbon (EC), organic carbon (OC), polycyclic aromatic hydrocarbons (PAHs), metals and ions) arising from these five cooking methods. To investigate the difference in particle properties of different cooking emissions, the amount and type of food, and the heat setting on the gas stove were kept constant during the entire course of the experiments. Results showed that deep-frying gave rise to the largest amount of PM 2.5 and most chemical components, followed by pan-frying, stir-frying, boiling, and steaming. Oil-based cooking methods released more organic pollutants (OC, PAHs, and organic ions) and metals, while water-based cooking methods accounted for more water-soluble (WS) ions. Their source profiles are also presented and discussed.

  9. Characterization of the chemical composition of PM2.5 emitted from on-road China III and China IV diesel trucks in Beijing, China.

    PubMed

    Wu, Bobo; Shen, Xianbao; Cao, Xinyue; Yao, Zhiliang; Wu, Yunong

    2016-05-01

    The composition of diesel exhaust fine particulate matter (PM2.5) is of growing interest because of its impacts on health and climatic factors and its application in source apportionment and aerosol modeling. We characterized the detailed chemical composition of the PM2.5, including the organic carbon (OC), elemental carbon (EC), water-soluble ions (WSIs), and elemental contents, emitted from China III and China IV diesel trucks (nine each) based on real-world measurements in Beijing using a portable emissions measurement system (PEMS). Carbonaceous compounds were the dominant components (totaling approximately 87%) of the PM2.5, similar to the results (greater than 80% of the PM2.5) of our previous study of on-road China III diesel trucks. In general, the amounts of individual component groups (carbonaceous compounds, WSIs, and elements) and PM2.5 emissions for China IV diesel trucks were lower than those of China III diesel trucks of the same size, except for the WSIs and elements for the light- and medium-duty diesel trucks. The EC/OC mass ratios were strongly dependent on the emission standards, and the ratios of China IV diesel trucks were higher than those of China III diesel trucks of the same size. The chemical species in the PM2.5 were significantly affected by the driving conditions. Overall, the emission factors (EFs) of the PM2.5 and OC under non-highway (NHW) driving conditions were higher than those under highway (HW) driving conditions, and the EC/OC mass ratios presented an increasing trend, with decreasing OC/PM2.5 and increasing EC/PM2.5 from NHW to HW driving conditions; similar trends were reported in our previous study. In addition, Pearson's correlation coefficients among the PM2.5 species were analyzed to determine the relationships among the various chemical components. Copyright © 2016 Elsevier B.V. All rights reserved.

  10. Global Chemical Composition of Ambient Fine Particulate Matter for Exposure Assessment

    SciTech Connect

    Philip, Sajeev; Martin, Randall V.; van Donkelaar, Aaron; Lo, Jason Wai-Ho; Wang, Yuxuan; Chen, Dan; Zhang, Lin; Kasibhatla, Prasad S.; Wang, Siwen; Zhang, Qiang; Lu, Zifeng; Streets, David G.; Bittman, Shabtai; Macdonald, Douglas J.

    2014-10-24

    Epidemiologic and health impact studies are inhibited by the paucity of global, long-term measurements of the chemical composition of fine particulate matter. We inferred PM2.5 chemical composition at 0.1° × 0.1° spatial resolution for 2004–2008 by combining aerosol optical depth retrieved from the MODIS and MISR satellite instruments, with coincident profile and composition information from the GEOS-Chem global chemical transport model. Evaluation of the satellite-model PM2.5 composition data set with North American in situ measurements indicated significant spatial agreement for secondary inorganic aerosol, particulate organic mass, black carbon, mineral dust, and sea salt. We found that global population-weighted PM2.5 concentrations were dominated by particulate organic mass (11.9 ± 7.3 μg/m3), secondary inorganic aerosol (11.1 ± 5.0 μg/m3), and mineral dust (11.1 ± 7.9 μg/m3). Secondary inorganic PM2.5 concentrations exceeded 30 μg/m3 over East China. Sensitivity simulations suggested that population-weighted ambient PM2.5 from biofuel burning (11 μg/m3) could be almost as large as from fossil fuel combustion sources (17 μg/m3). In conclusion, these estimates offer information about global population exposure to the chemical components and sources of PM2.5.

  11. CHARACTERIZING THE SOURCES OF HUMAN EXPOSURE TO MUTAGENIC AND CARCINOGENIC CHEMICALS IN AIRBORNE FINE PARTICLES

    EPA Science Inventory

    Personal and ambient exposures to airborne fine particles, polycyclic aromatic hydrocarbons (PAH), and genotoxic activity has been studied in populations in the US, Japan, China, and the Czech Republic. Personal exposure monitors used to collect fine particles were extracted f...

  12. CHARACTERIZING THE SOURCES OF HUMAN EXPOSURE TO MUTAGENIC AND CARCINOGENIC CHEMICALS IN AIRBORNE FINE PARTICLES

    EPA Science Inventory

    Personal and ambient exposures to airborne fine particles, polycyclic aromatic hydrocarbons (PAH), and genotoxic activity has been studied in populations in the US, Japan, China, and the Czech Republic. Personal exposure monitors used to collect fine particles were extracted f...

  13. Chemical characterization and source apportionment of fine and coarse particulate matter in Lahore, Pakistan

    NASA Astrophysics Data System (ADS)

    Stone, Elizabeth; Schauer, James; Quraishi, Tauseef A.; Mahmood, Abid

    2010-03-01

    Lahore, Pakistan is an emerging megacity that is heavily polluted with high levels of particle air pollution. In this study, respirable particulate matter (PM 2.5 and PM 10) were collected every sixth day in Lahore from 12 January 2007 to 19 January 2008. Ambient aerosol was characterized using well-established chemical methods for mass, organic carbon (OC), elemental carbon (EC), ionic species (sulfate, nitrate, chloride, ammonium, sodium, calcium, and potassium), and organic species. The annual average concentration (±one standard deviation) of PM 2.5 was 194 ± 94 μg m -3 and PM 10 was 336 ± 135 μg m -3. Coarse aerosol (PM 10-2.5) was dominated by crustal sources like dust (74 ± 16%, annual average ± one standard deviation), whereas fine particles were dominated by carbonaceous aerosol (organic matter and elemental carbon, 61 ± 17%). Organic tracer species were used to identify sources of PM 2.5 OC and chemical mass balance (CMB) modeling was used to estimate relative source contributions. On an annual basis, non-catalyzed motor vehicles accounted for more than half of primary OC (53 ± 19%). Lesser sources included biomass burning (10 ± 5%) and the combined source of diesel engines and residual fuel oil combustion (6 ± 2%). Secondary organic aerosol (SOA) was an important contributor to ambient OC, particularly during the winter when secondary processing of aerosol species during fog episodes was expected. Coal combustion alone contributed a small percentage of organic aerosol (1.9 ± 0.3%), but showed strong linear correlation with unidentified sources of OC that contributed more significantly (27 ± 16%). Brick kilns, where coal and other low quality fuels are burned together, are suggested as the most probable origins of unapportioned OC. The chemical profiling of emissions from brick kilns and other sources unique to Lahore would contribute to a better understanding of OC sources in this megacity.

  14. Fine particulate matter source apportionment using a hybrid chemical transport and receptor model approach

    NASA Astrophysics Data System (ADS)

    Hu, Y.; Balachandran, S.; Pachon, J. E.; Baek, J.; Ivey, C.; Holmes, H.; Odman, M. T.; Mulholland, J. A.; Russell, A. G.

    2013-10-01

    A hybrid fine particulate matter (PM2.5) source apportionment approach based on a receptor-model (RM) species balance and species specific source impacts from a chemical transport model (CTM) equipped with a sensitivity analysis tool is developed to provide physically- and chemically-consistent relationships between source emissions and receptor impacts. This hybrid approach enhances RM results by providing initial estimates of source impacts from a much larger number of sources than are typically used in RMs, and provides source-receptor relationships for secondary species. Further, the method addresses issues of source collinearities, and accounts for emissions uncertainties. Hybrid method results also provide information on the resulting source impact uncertainties. We apply this hybrid approach to conduct PM2.5 source apportionment at Chemical Speciation Network (CSN) sites across the US. Ambient PM2.5 concentrations at these receptor sites were apportioned to 33 separate sources. Hybrid method results led to large changes of impacts from CTM estimates for sources such as dust, woodstove, and other biomass burning sources, but limited changes to others. The refinements reduced the differences between CTM-simulated and observed concentrations of individual PM2.5 species by over 98% when using a weighted least squared error minimization. The rankings of source impacts changed from the initial estimates, revealing that CTM-only results should be evaluated with observations. Assessment with RM results at six US locations showed that the hybrid results differ somewhat from commonly resolved sources. The hybrid method also resolved sources that typical RM methods do not capture without extra measurement information on unique tracers. The method can be readily applied to large domains and long (such as multi-annual) time periods to provide source impact estimates for management- and health-related studies.

  15. Fine particulate matter source apportionment using a hybrid chemical transport and receptor model approach

    NASA Astrophysics Data System (ADS)

    Hu, Y.; Balachandran, S.; Pachon, J. E.; Baek, J.; Ivey, C.; Holmes, H.; Odman, M. T.; Mulholland, J. A.; Russell, A. G.

    2014-06-01

    A hybrid fine particulate matter (PM2.5) source apportionment approach based on a receptor model (RM) species balance and species specific source impacts from a chemical transport model (CTM) equipped with a sensitivity analysis tool is developed to provide physically and chemically consistent relationships between source emissions and receptor impacts. This hybrid approach enhances RM results by providing initial estimates of source impacts from a much larger number of sources than are typically used in RMs, and provides source-receptor relationships for secondary species. Further, the method addresses issues of source collinearities and accounts for emissions uncertainties. We apply this hybrid approach to conduct PM2.5 source apportionment at Chemical Speciation Network (CSN) sites across the US. Ambient PM2.5 concentrations at these receptor sites were apportioned to 33 separate sources. Hybrid method results led to large changes of impacts from CTM estimates for sources such as dust, woodstoves, and other biomass-burning sources, but limited changes to others. The refinements reduced the differences between CTM-simulated and observed concentrations of individual PM2.5 species by over 98% when using a weighted least-squares error minimization. The rankings of source impacts changed from the initial estimates, further demonstrating that CTM-only results should be evaluated with observations. Assessment with RM results at six US locations showed that the hybrid results differ somewhat from commonly resolved sources. The hybrid method also resolved sources that typical RM methods do not capture without extra measurement information for unique tracers. The method can be readily applied to large domains and long (such as multi-annual) time periods to provide source impact estimates for management- and health-related studies.

  16. The chemical composition of fine ambient aerosol particles in the Beijing area

    NASA Astrophysics Data System (ADS)

    Nekat, Bettina; van Pinxteren, Dominik; Iinuma, Yoshiteru; Gnauk, Thomas; Müller, Konrad; Herrmann, Hartmut

    2010-05-01

    The strong economical growth in China during the last few decades led to heavy air pollution caused by significantly increased particle emissions. The aerosol particles affect not only the regional air quality and visibility, but can also influence cloud formation processes and the radiative balance of the atmosphere by their optical and microphysical properties. The ability to act as Cloud Condensation Nuclei (CCN) is related to microphysical properties like the hygroscopic growth or the cloud droplet activation. The chemical composition of CCN plays an important role on these properties and varies strongly with the particle size and the time of day. Hygroscopic or surface active substances can increase the hygroscopicity and lower the surface tension of the particle liquid phase, respectively. The presence of such compounds may result in faster cloud droplet activation by faster water uptake. The DFG project HaChi (Haze in China) aimed at studying physical and chemical parameters of urban aerosol particles in the Beijing area in order to associate the chemical composition of aerosol particles with their ability to act as CCN. To this end, two measurement campaigns were performed at the Wuqing National Ordinary Meteorological Observing Station, which is a background site near Beijing. The winter campaign was realized in March 2009 and the summer campaign took place from mid July 2009 to mid August 2009. Fine particles with an aerodynamic diameter smaller than or equal 1 μm were continuously sampled for 24h over the two campaigns using a DIGITEL high volume sampler (DHA-80). The present contribution presents and discusses the results of the chemical characterization of the DIGITEL filters samples. The filters were analyzed for the mass concentration, inorganic ions and carbon sum parameters like elemental (EC), organic (OC) and water soluble organic carbon (WSOC). The WSOC fraction was further characterized for hygroscopic substances like low molecular

  17. Friction and Wear of Ion-Beam-Deposited Diamondlike Carbon on Chemical-Vapor-Deposited, Fine-Grain Diamond

    NASA Technical Reports Server (NTRS)

    Miyoshi, Kazuhisa; Wu, Richard L. C.; Lanter, William C.

    1996-01-01

    Friction and wear behavior of ion-beam-deposited diamondlike carbon (DLC) films coated on chemical-vapor-deposited (CVD), fine-grain diamond coatings were examined in ultrahigh vacuum, dry nitrogen, and humid air environments. The DLC films were produced by the direct impact of an ion beam (composed of a 3:17 mixture of Ar and CH4) at ion energies of 1500 and 700 eV and an RF power of 99 W. Sliding friction experiments were conducted with hemispherical CVD diamond pins sliding on four different carbon-base coating systems: DLC films on CVD diamond; DLC films on silicon; as-deposited, fine-grain CVD diamond; and carbon-ion-implanted, fine-grain CVD diamond on silicon. Results indicate that in ultrahigh vacuum the ion-beam-deposited DLC films on fine-grain CVD diamond (similar to the ion-implanted CVD diamond) greatly decrease both the friction and wear of fine-grain CVD diamond films and provide solid lubrication. In dry nitrogen and in humid air, ion-beam-deposited DLC films on fine-grain CVD diamond films also had a low steady-state coefficient of friction and a low wear rate. These tribological performance benefits, coupled with a wider range of coating thicknesses, led to longer endurance life and improved wear resistance for the DLC deposited on fine-grain CVD diamond in comparison to the ion-implanted diamond films. Thus, DLC deposited on fine-grain CVD diamond films can be an effective wear-resistant, lubricating coating regardless of environment.

  18. Chemical characterization of fine organic aerosol for source apportionment at Monterrey, Mexico

    NASA Astrophysics Data System (ADS)

    Mancilla, Y.; Mendoza, A.; Fraser, M. P.; Herckes, P.

    2015-07-01

    , source attribution results obtained using the CMB model indicate that emissions from motor vehicle exhausts are the most important, accounting for the 64 % of the PM2.5. The vegetative detritus and biomass burning had the smallest contribution (2.2 % of the PM2.5). To our knowledge, this is the second study to explore the broad chemical characterization of fine organic aerosol in Mexico and the first for the MMA.

  19. The Open Cluster Chemical Abundances and Mapping (OCCAM) Survey: Galactic Gradients using SDSS-IV/DR13 and Gaia

    NASA Astrophysics Data System (ADS)

    Frinchaboy, Peter M.; Donor, John; O'Connell, Julia; Cunha, Katia M. L.; Thompson, Benjamin A.; Melendez, Matthew; Shetrone, Matthew D.; Majewski, Steven R.; Zasowski, Gail; Allende-Prieto, Carlos; Carrera, Ricardo; García Pérez, Ana; Hayden, Michael R.; Hearty, Fred R.; Holtzman, Jon A.; Johnson, Jennifer; Meszaros, Szabolcs; Nidever, David L.; Pinsonneault, Marc H.; Roman-Lopes, Alexandre; Schiavon, Ricardo P.; Schultheis, Mathias; Smith, Verne V.; Sobeck, Jennifer; Stassun, Keivan G.; APOGEE Team

    2017-01-01

    The Open Cluster Chemical Analysis and Mapping (OCCAM) survey aims to produce a comprehensive, uniform, infrared-based data set forhundreds of open clusters, and constrain key Galactic dynamical and chemical parameters using the SDSS/APOGEE survey. We report on multi-element radial abundance gradients obtained from a sample of over 30 disk open clusters. The chemical abundances were derived automatically by the ASPCAP pipeline and these are part of the SDSS IV Data Release 13. The open cluster sample studied spans a significant range in age allowing exploration of the evolution of the Galactic abundance gradient.This work is supported by an NSF AAG grant AST-1311835.

  20. Fine particulate matter and visibility in the Lake Tahoe Basin: chemical characterization, trends, and source apportionment.

    PubMed

    Green, Mark C; Chen, L W Antony; DuBois, David W; Molenar, John V

    2012-08-01

    Speciated PM2.5 (particulate matter with an aerodynamic diameterFine mass at SOLA is 2.5 times that at BLIS, mainly due to enhanced organic and elemental carbon (OC and EC). SOLA experiences a winter peak in PM25 mainly due to OC and EC from residential wood combustion, whereas BLIS experiences a summer peak in PM2.5 mainly due to OC and ECfrom wildfires. Carbonaceous aerosol dominates visibility impairment, causing about 1/2 the reconstructed aerosol light extinction at BLIS and 70% at SOLA. Trend analysis (1990-2009) showed statistically significant decreases in aerosol extinction at BLIS on 20% best and 60% middle visibility days and statistically insignificant upward trends on 20% worst days. SOLA (1990-2003) showed statistically significant decreases in aerosol extinction for all day categories, driven by decreasing OC and EC. From the regional haze rule baseline period of 2000-2004 until 2005-2009, BLIS saw 20% best days improving and 20% worst days getting worse due to increased wildfire effects. Receptor modeling was performed using positive matrix factorization (PMF) and chemical mass balance (CMB). It confirmed that (1) biomass burning dominanted PM25 sources at both sites with increasing importance over time; (2) low combustion efficiency burning accounts for most of the biomass burning contribution; (3) road dust and traffic contributions were much higher at SOLA than at BLIS; and (4) industrial combustion and salting were minor sources.

  1. Electrochemical treatment of the effluent of a fine chemical manufacturing plant.

    PubMed

    Cañizares, P; Paz, R; Lobato, J; Sáez, C; Rodrigo, M A

    2006-11-02

    In this work, the electrochemical oxidation of an actual industrial wastewater with conductive-diamond anodes has been studied. The wastewater is the effluent of a fine chemicals plant. This effluent consists of an aqueous solution of solvents (ketones and alcohols) with a high concentration of aromatic compounds coming from the raw materials, intermediates and products of the different processes of the plant and its COD is around 6000 mg dm(-3). The electrolyses were carried out in a discontinuous operation mode under galvanostatic conditions, using a bench-scale plant equipped with a single compartment electrochemical flow cell. The conductive-diamond electrochemical oxidation (CDEO) allowed achieving the complete mineralization of the waste with high current efficiencies. These efficiencies seem to strongly depend on the concentration, pH and temperature but not on the current density (in the range studied). This confirms that besides the hydroxyl radicals mediated oxidation, CDEO combines other important oxidation processes such as the direct electrooxidation on the diamond surface and the oxidation mediated by other electrochemically formed compounds generated on this electrode. Other two advanced oxidation processes (ozonation and Fenton oxidation) have been also studied in this work for comparison purposes. Both technologies were able to treat the wastes, but they obtained very different results in terms of efficiency and mineralization. The efficiency of ozonation and electrochemical oxidation were very similar (especially during the first stages), although the energy consumption required by the electrochemical process to remove at fixed percentage of COD or TOC was significantly smaller than that of ozonation. The possible accumulation of carboxylic acid as final products excludes the use of Fenton oxidation as a sole treatment technology.

  2. Effects of chemical dispersants and mineral fines on crude oil dispersion in a wave tank under breaking waves.

    PubMed

    Li, Zhengkai; Kepkay, Paul; Lee, Kenneth; King, Thomas; Boufadel, Michel C; Venosa, Albert D

    2007-07-01

    The interaction of chemical dispersants and suspended sediments with crude oil influences the fate and transport of oil spills in coastal waters. A wave tank study was conducted to investigate the effects of chemical dispersants and mineral fines on the dispersion of oil and the formation of oil-mineral-aggregates (OMAs) in natural seawater. Results of ultraviolet spectrofluorometry and gas chromatography flame ionized detection analysis indicated that dispersants and mineral fines, alone and in combination, enhanced the dispersion of oil into the water column. Measurements taken with a laser in situ scattering and transmissometer (LISST-100X) showed that the presence of mineral fines increased the total concentration of the suspended particles from 4 to 10microl l(-1), whereas the presence of dispersants decreased the particle size (mass mean diameter) of OMAs from 50 to 10microm. Observation with an epifluorescence microscope indicated that the presence of dispersants, mineral fines, or both in combination significantly increased the number of particles dispersed into the water.

  3. Permeability Enhancement in Fine-Grained Sediments by Chemically Induced Clay Fabric Shrinkage

    SciTech Connect

    Wijesinghe, A M; Kansa, E J; Viani, B E; Blake, R G; Roberts, J J; Huber, R D

    2004-02-26

    The National Research Council [1] identified the entrapment of contaminants in fine-grained clay-bearing soils as a major impediment to the timely and cost-effective remediation of groundwater to regulatory standards. Contaminants trapped in low-permeability, low-diffusivity, high-sorptivity clays are not accessible to advective flushing by treatment fluids from permeable zones, and slowly diffuse out to recontaminate previously cleaned permeable strata. We propose to overcome this barrier to effective remediation by exploiting the ability of certain nontoxic EPA-approved chemicals (e.g., ethanol) to shrink and alter the fabric of clays, and thereby create macro-porosity and crack networks in fine-grained sediments. This would significantly reduce the distance and time scales of diffusive mass transport to advectively flushed boundaries, to yield orders of magnitude reduction in the time required to complete remediation. Given that effective solutions to this central problem of subsurface remediation do not yet exist, the cost and time benefits of successful deployment of this novel concept, both as a stand-alone technology and as an enabling pre-treatment for other remedial technologies that rely on advective delivery, is likely to be very large. This project, funded as a 1-year feasibility study by LLNL's LDRD Program, is a multi-directorate, multi-disciplinary effort that leverages expertise from the Energy & Environment Directorate, the Environmental Restoration Division, and the Manufacturing & Materials Evaluation Division of Mechanical Engineering. In this feasibility study, a ''proof-of-principle'' experiment was performed to answer the central question: ''Can clay shrinkage induced by ethanol in clay-bearing sediments overcome realistic confining stresses, crack clay, and increase its effective permeability by orders of magnitude within a time that is much smaller than the time required for diffusive mass transport of ethanol in the unaltered sediment

  4. Chemical characterization of the fine particle emissions from commercial aircraft engines during the Aircraft Particle Emissions eXperiment (APEX) 1 to 3.

    PubMed

    Kinsey, J S; Hays, M D; Dong, Y; Williams, D C; Logan, R

    2011-04-15

    This paper addresses the need for detailed chemical information on the fine particulate matter (PM) generated by commercial aviation engines. The exhaust plumes of seven turbofan engine models were sampled as part of the three test campaigns of the Aircraft Particle Emissions eXperiment (APEX). In these experiments, continuous measurements of black carbon (BC) and particle surface-bound polycyclic aromatic compounds (PAHs) were conducted. In addition, time-integrated sampling was performed for bulk elemental composition, water-soluble ions, organic and elemental carbon (OC and EC), and trace semivolatile organic compounds (SVOCs). The continuous BC and PAH monitoring showed a characteristic U-shaped curve of the emission index (EI or mass of pollutant/mass of fuel burned) vs fuel flow for the turbofan engines tested. The time-integrated EIs for both elemental composition and water-soluble ions were heavily dominated by sulfur and SO(4)(2-), respectively, with a ∼2.4% median conversion of fuel S(IV) to particle S(VI). The corrected OC and EC emission indices obtained in this study ranged from 37 to 83 mg/kg and 21 to 275 mg/kg, respectively, with the EC/OC ratio ranging from ∼0.3 to 7 depending on engine type and test conditions. Finally, the particle SVOC EIs varied by as much as 2 orders of magnitude with distinct variations in chemical composition observed for different engine types and operating conditions.

  5. Speciated fine particulate matter in Northern Italy: A whole year chemical and transport modelling reconstruction

    NASA Astrophysics Data System (ADS)

    Lonati, G.; Pirovano, G.; Sghirlanzoni, G. A.; Zanoni, A.

    2010-03-01

    The so-called "one atmosphere modelling approach" is applied over a mesoscale domain and model outputs for gaseous pollutants (NO X and O 3) and for size resolved PM mass concentration (PM10 and PM2.5) are compared to observed data time series at reference sites representative of different locations (urban, suburban and rural sites) throughout the modelling domain. The CAMx model (Comprehensive Air quality Model with eXtensions) was used for simulation over the Po valley air basin with a 10 × 10 km 2 spatial resolution based on emission and meteorological data for the 01/04/2003-31/03/2004 period. Model results for speciated PM2.5 mass concentration (including nitrate, sulphate, ammonium, elemental carbon and organic matter) are compared to artefact-corrected data from campaigns performed for the city of Milan and its neighbourhoods. Since model results are not concurrent with the available PM2.5 measurements, bootstrapping technique is applied in order to extract from model results restricted warm-season and cold-season data populations suitable for quantitative comparison with measured data. The model seems able to correctly reproduce the spatial distribution and the local concentration gradients of both PM10 and PM2.5 bulk mass with high concentration levels on the Po valley, increasing around urban areas. However, the comparison with experimental data shows relevant underestimations of PM10 and PM2.5 concentrations, especially at the most polluted urban "hot spots", where underestimations rise up to 60% of the actual PM levels. Speciated PM2.5 results, still in agreement with local composition gradients, point out that PM mass underestimations essentially derive from a 60% underestimation of organic matter (in both seasons) and sulphate (cold season only) concentrations, whereas a rather good agreement is observed for the other chemical species and especially for the ammonium-nitrate system. Such results suggest to better refine emission inventory data, with

  6. Characterizing chemical transport of ozone and fine particles in the Great Lakes region

    NASA Astrophysics Data System (ADS)

    Spak, Scott N.

    This dissertation presents a science framework relevant to evaluating impacts of land use policy scenarios, energy technologies, and climate on urban and regional air quality. Emerging from collaboration with urban planners, this work provides a means for employing atmospheric chemical transport modeling to understand environmental ramifications of long-term, spatially disaggregated changes in population and automobile emissions at the census tract level, and to assess the sensitivity of these changes to densification strategies. Toward these goals, the framework is used to evaluate model skill in resolving contemporary characteristics of ozone (O3) and speciated fine particles (PM2.5) in the Great Lakes region of North America, and to quantitatively explore meteorological processes that bring about observed features of these pollutants in the region. The Great Lakes were chosen due to a population concentrated in sprawling metropolitan areas, consistently high and widespread pollutant burdens, and seasonal effects of the lakes on the atmosphere. In annual simulation at 36 km resolution, the Community Multiscale Air Quality model is evaluated using speciated PM2.5 measurements taken at regulatory monitoring networks orientated to sample urban, rural, and remote areas. Performance relative to ad-hoc regional modeling goals and prior studies is average to excellent for most species throughout the year. Both pollution episodes and seasonality are captured. The Great Lakes affect pollution seasonality: strong winds advect aerosols around the deep marine boundary layer to lower surface PM2.5 in fall and winter, while O3 over the lakes is enhanced throughout the year, driven by temperature in the cool seasons and lake breeze circulation in spring and summer. Simulations confirm observational evidence that rural and small-city sources are responsible for most regional PM2.5. Sensitivities to urban and rural reductions are of comparable magnitude on a percentage basis

  7. Chemical analysis of World Trade Center fine particulate matter for use in toxicologic assessment.

    PubMed

    McGee, John K; Chen, Lung Chi; Cohen, Mitchell D; Chee, Glen R; Prophete, Colette M; Haykal-Coates, Najwa; Wasson, Shirley J; Conner, Teri L; Costa, Daniel L; Gavett, Stephen H

    2003-06-01

    The catastrophic destruction of the World Trade Center (WTC) on 11 September 2001 caused the release of high levels of airborne pollutants into the local environment. To assess the toxicity of fine particulate matter [particulate matter with a mass median aerodynamic diameter < 2.5 microm (PM2.5)], which may adversely affect the health of workers and residents in the area, we collected fallen dust samples on 12 and 13 September 2001 from sites within a half-mile of Ground Zero. Samples of WTC dust were sieved, aerosolized, and size-separated, and the PM2.5 fraction was isolated on filters. Here we report the chemical and physical properties of PM2.5 derived from these samples and compare them with PM2.5 fractions of three reference materials that range in toxicity from relatively inert to acutely toxic (Mt. St. Helens PM; Washington, DC, ambient air PM; and residual oil fly ash). X-ray diffraction of very coarse sieved WTC PM (< 53 microm) identified calcium sulfate (gypsum) and calcium carbonate (calcite) as major components. Scanning electron microscopy confirmed that calcium-sulfur and calcium-carbon particles were also present in the WTC PM2.5 fraction. Analysis of WTC PM2.5 using X-ray fluorescence, neutron activation analysis, and inductively coupled plasma spectrometry showed high levels of calcium (range, 22-33%) and sulfur (37-43% as sulfate) and much lower levels of transition metals and other elements. Aqueous extracts of WTC PM2.5 were basic (pH range, 8.9-10.0) and had no evidence of significant bacterial contamination. Levels of carbon were relatively low, suggesting that combustion-derived particles did not form a significant fraction of these samples recovered in the immediate aftermath of the destruction of the towers. Because gypsum and calcite are known to cause irritation of the mucus membranes of the eyes and respiratory tract, inhalation of high doses of WTC PM2.5 could potentially cause toxic respiratory effects.

  8. Chemical analysis of World Trade Center fine particulate matter for use in toxicologic assessment.

    PubMed Central

    McGee, John K; Chen, Lung Chi; Cohen, Mitchell D; Chee, Glen R; Prophete, Colette M; Haykal-Coates, Najwa; Wasson, Shirley J; Conner, Teri L; Costa, Daniel L; Gavett, Stephen H

    2003-01-01

    The catastrophic destruction of the World Trade Center (WTC) on 11 September 2001 caused the release of high levels of airborne pollutants into the local environment. To assess the toxicity of fine particulate matter [particulate matter with a mass median aerodynamic diameter < 2.5 microm (PM2.5)], which may adversely affect the health of workers and residents in the area, we collected fallen dust samples on 12 and 13 September 2001 from sites within a half-mile of Ground Zero. Samples of WTC dust were sieved, aerosolized, and size-separated, and the PM2.5 fraction was isolated on filters. Here we report the chemical and physical properties of PM2.5 derived from these samples and compare them with PM2.5 fractions of three reference materials that range in toxicity from relatively inert to acutely toxic (Mt. St. Helens PM; Washington, DC, ambient air PM; and residual oil fly ash). X-ray diffraction of very coarse sieved WTC PM (< 53 microm) identified calcium sulfate (gypsum) and calcium carbonate (calcite) as major components. Scanning electron microscopy confirmed that calcium-sulfur and calcium-carbon particles were also present in the WTC PM2.5 fraction. Analysis of WTC PM2.5 using X-ray fluorescence, neutron activation analysis, and inductively coupled plasma spectrometry showed high levels of calcium (range, 22-33%) and sulfur (37-43% as sulfate) and much lower levels of transition metals and other elements. Aqueous extracts of WTC PM2.5 were basic (pH range, 8.9-10.0) and had no evidence of significant bacterial contamination. Levels of carbon were relatively low, suggesting that combustion-derived particles did not form a significant fraction of these samples recovered in the immediate aftermath of the destruction of the towers. Because gypsum and calcite are known to cause irritation of the mucus membranes of the eyes and respiratory tract, inhalation of high doses of WTC PM2.5 could potentially cause toxic respiratory effects. PMID:12782501

  9. Chemical weathering trends in fine-grained ephemeral stream sediments of the McMurdo Dry Valleys, Antarctica

    NASA Astrophysics Data System (ADS)

    Marra, Kristen R.; Elwood Madden, Megan E.; Soreghan, Gerilyn S.; Hall, Brenda L.

    2017-03-01

    We investigated chemical weathering trends within the fine-grained (< 63 μm; silt and clay) fraction of sediments collected from meltwater streams emanating from glaciers in the McMurdo Dry Valleys (MDV; Wright and Taylor Valleys) by integrating grain size, BET surface area, and whole-rock geochemistry. While both valleys currently host cold-based glaciers, the sediment underlying the ephemeral glacial streams was deposited under differing glacial conditions. In Wright Valley (Clark Glacier stream), Brownworth and Trilogy drifts were deposited via cold-based glaciation, whereas the Ross Sea drift that underlies Delta Stream in Taylor Valley likely reflects contributions from wet-based ice. Wright Valley stream sediments are typically coarser grained and have a higher silt content as compared to Taylor Valley sediments. These sediments consist primarily of pyroxenes, quartz, and feldspars, with the percentages of pyroxenes and quartz systematically increasing downstream. The percentage of phyllosilicates ranges from 4 to 18% and decreases with downstream distance. In contrast, Taylor Valley sediments (Delta Stream) are finer-grained and exhibit lower percentages of both pyroxene and quartz and a significantly higher percentage of phyllosilicates (30-43%). Concentrations of all mineral phases remain relatively consistent in abundance with downstream transport in the Delta Stream transect as compared to Clark Glacier stream sediments. Standard chemical weathering indices, such as the Chemical Index of Alteration (CIA), indicate that chemical weathering is occurring within the silt and clay fractions of Antarctic stream sediments and is particularly pronounced in Delta Stream sediments that have BET surface area measurements > 40 m2/g. Utilization of MFW (mafic-felsic-weathered) and A-CN-K (Al2O3-CaO + Na2O-K2O) plots, however, are more effective in discerning the extent and nature of chemical weathering in these stream systems. Ca and Na depletion observed within the

  10. Chemical composition of emissions from urban sources of fine organic aerosol

    SciTech Connect

    Hildemann, L.M.; Markowski, G.R.; Cass, G.R. )

    1991-04-01

    A dilution source sampling system was used to collect primary fine aerosol emissions from important sources of urban organic aerosol, including a boiler burning No. 2 fuel oil, a home fireplace, a fleet of catalyst-equipped and noncatalyst automobiles, heavy-duty diesel trucks, natural gas home appliances, and meat cooking operations. Alternative dilution sampling techniques were used to collect emissions from cigarette smoking and a roofing tar pot, and grab sample techniques were employed to characterize paved road dust, brake lining wear, and vegetative detritus. Organic aerosol constituted the majority of the fine aerosol mass emitted from many of the sources tested. Fine primary organic aerosol emissions within the heavily urbanized western portion of the Los Angeles Basin were determined to total 29.8 metric ton/day. Over 40% of these organic aerosol emissions are from anthropogenic pollution sources that are expected to emit contemporary (nonfossil) aerosol carbon, in good agreement with the available ambient monitoring data.

  11. An optical chemical sensor for thorium (IV) determination based on thorin.

    PubMed

    Rastegarzadeh, S; Pourreza, N; Saeedi, I

    2010-01-15

    A selective method for the determination of thorium (IV) using an optical sensor is described. The sensing membrane is prepared by immobilization of thorin-methyltrioctylammonium ion pair on triacetylcellulose polymer. The sensor produced a linear response for thorium (IV) concentration in the range of 6.46 x 10(-6) to 9.91 x 10(-5)mol L(-1) with detection limit of 1.85 x 10(-6)mol L(-1). The regeneration of optode was accomplished completely at a short time (less than 20s) with 0.1 mol L(-1) of oxalate ion solution. The relative standard deviation for ten replicate measurements of 2.15 x 10(-5) and 8.62 x 10(-5)mol L(-1) of thorium was 2.71 and 1.65%, respectively. The optode membrane exhibits good selectivity for thorium (IV) over several other ionic species and are comparable to those obtained in case of spectrophotometric determination of thorium using thorin in solution. A good agreement with the ICP-MS and spiked method was achieved when the proposed optode was applied to the determination of thorium (IV) in dust and water samples.

  12. Chemical mass balance source apportionment of fine and PM10 in the Desert Southwest, USA

    EPA Science Inventory

    The Desert Southwest Coarse Particulate Matter Study was undertaken in Pinal County, Arizona, to better understand the origin and impact of sources of fine and coarse particulate matter (PM) in rural, arid regions of the U.S. southwestern desert. The desert southwest experiences ...

  13. Chemical mass balance source apportionment of fine and PM10 in the Desert Southwest, USA

    EPA Science Inventory

    The Desert Southwest Coarse Particulate Matter Study was undertaken in Pinal County, Arizona, to better understand the origin and impact of sources of fine and coarse particulate matter (PM) in rural, arid regions of the U.S. southwestern desert. The desert southwest experiences ...

  14. Using the Photolysis of Chemically Modified Gel Films Preparing ITO Fine Patterned Thin Films

    NASA Astrophysics Data System (ADS)

    Li, Ying; Zhao, Gaoyang; Zhang, Weihua; Chen, Yuanqing

    2006-06-01

    A novel technique for the fabrication of tin-doped indium oxide (ITO) fine patterning in sol-gel technology is presented in this paper. The fabricated ITO fine patterning could be obtained through a process which combines film fabrication with film etching. ITO films have good comprehensive property of visible transmittance and electrical conductivity, consequently they have been extensively used as coating electrodes. Indium nitrate (In(NO3)3.4.5H2O) and stannic chloride (SnCl4.5H2O) were used as starting materials which were modified with benzytone (BzAcH). The chelate complexes containing indium ions were produced during the process which of forming photosensitive ITO/BzAcH gel films through sol-gel technique. It was found that the gel films are sensitive to both the ultraviolet (UV) light irradiation and their solubility on solvents as well. For example, ethanol was reduced remarkably while the UV absorption peak disappeared with the dissociation of the chelate complexes correspondingly by means of UV-vis and IR spectrophotometers. Utilizing these characteristics, a fine pattern was obtained by irradiation of UV light on the ITO/BzAcH gel films through a pattern mask. of the fine patterned ITO films were heat treated at 500 °C for 15 min, the optical, electrical properties and the surface element components were examined by X-ray photoelectron spectroscopy (XPS) spectra in this work.

  15. Chemical dispersion of oil with mineral fines in a low temperature environment.

    PubMed

    Wang, Weizhi; Zheng, Ying; Lee, Kenneth

    2013-07-15

    The increasing risks of potential oil spills in the arctic regions, which are characterized by low temperatures, are a big challenge. The traditional dispersant method has shown limited effectiveness in oil cleanup. This work studied the role of mineral fines in the formation of oil-mineral aggregates (OMAs) at low temperature (0-4 °C) environment. The loading amount of minerals and dispersant with different dispersant and oil types were investigated under a full factorial design. The shapes and sizes of OMAs were analyzed. Results showed that the behavior of OMA formation differs when dispersant and mineral fines are used individually or together. Both the experimental and microscopic results also showed the existence of optimal dispersant to oil ratios and mineral to oil ratios. In general, poor oil removal performance was observed for more viscous oil. Corexit 9500 performed better than Corexit 9527 with various oils, in terms of oil dispersion and OMA formation.

  16. Comparison of a 4000-reaction chemical mechanism with the carbon bond IV and an adjusted carbon bond IV-EX mechanism using SMVGEAR II

    NASA Astrophysics Data System (ADS)

    Liang, Jinyou; Jacobson, Mark Z.

    The well-known carbon bond IV (CBIV) chemical mechanism (33 species, 81 reactions) is compared with an adjusted carbon bond mechanism (ACBM) (109 species, 233 reactions) and a more explicit master chemical mechanism (MCM) (1427 species, 3911 reactions) in tests of their predictions of O 3, NO x(=NO+NO 2), HCHO, HNO 3, H 2O 2, and peroxyacetlynitrate (PAN). The ACBM was developed from a fourth mechanism, the expanded carbon bond mechanism (CBM-EX), by explicitly including the decomposition of C 2H 6, C 3H 8, and C 3H 6. All three mechanisms tested were updated with the inorganic chemistry from the ACBM and implemented into the sparse-matrix, ordinary differential equation solver, SMVGEAR II. Sparse-matrix treatment in SMVGEAR II reduced the number of calculations during matrix decomposition for the MCM by a factor of 15,000 (99.995%), or from an estimated 154 h to 37 s of cpu time per simulation day in one grid cell on an SGI origin 2000, in comparison with a full-matrix solution. Computer time for each mechanism was linearly proportional to the number of species in the mechanism. It is shown that the three mechanisms agreed closely when aromatic concentrations were initially low in comparison with alkane, alkene, and aldehyde initial concentrations. When aromatic concentrations were initially high (higher than that observed in urban air), the yields of O 3, HCHO, and PAN differed significantly among the three mechanisms although the daily maximum concentrations of these species agreed better. The aromatic representation in MCM appears to lead to systematic overprediction of ozone, according to a comparison with smog chamber data. For initial conditions taken from measurements at nine sites in Los Angeles, the daily maximum concentrations of O 3, HCHO, PAN, and H 2O 2 predicted by the three mechanisms differed by 30-50%, 10-40%, 15-40%, and 60-80%, respectively. The relative differences between the daytime series of O 3, HCHO, H 2O 2, and PAN predicted by the three

  17. Ecological effects and chemical composition of fine sediments in Upper Austrian streams and resulting implications for river management

    NASA Astrophysics Data System (ADS)

    Höfler, Sarah; Pichler-Scheder, Christian; Gumpinger, Clemens

    2017-04-01

    In the current scientific discussion high loads of fine sediments are considered one of the most important causes of river ecosystem degradation worldwide. Especially in intensively used catchment areas changes in the sediment household must be regarded as a reason, which prevents the achievement of the objectives of the European Water Framework Directive (WFD). Therefore, the Upper Austrian Water Authorities have launched two comprehensive studies on the topic. The first one was a survey on the current siltation status of river courses in Upper Austria. The second study deals with two selected catchments in detail, in order to get a clear picture of the impacts of the fines on the aquatic fauna (trout eggs, benthic invertebrates), the chemical composition of these fractions, the crucial hydrogeological processes and to develop possible role models for measures both in the catchments and in the streams. At eight sites within the two catchments sediment and water samples were collected at two dates for detailed chemical analysis. On one date additionally the benthic invertebrate fauna was investigated on the microhabitat level. Thereby it was possible to enhance the understanding of the range of ecological impacts caused by silting-up in different hydro-morphological circumstances and with different fine sediment loads. The water samples as well as the sediment fraction samples <0.063 mm were examined for different metals, organochlorine pesticides, PAHs (Polycyclic Aromatic Hydrocarbons), PCBs (Polychlorinated biphenyls), BTEX (benzene, toluene, ethylbenzene, and xylenes), AOX (adsorbable organohalogens) and various nutrients. Additionally, the basic parameters dry residue, loss on ignition, TC (total carbon), TOC (total organic carbon) and nutrients were analysed. From the sediment eluates and the filtered water decomposition products of pesticides, remains of medical drugs, sweeteners, hormonally active substances and water-soluble elements were analysed

  18. Chemical diversity among fine-grained soils at Gale (Mars): a chemical transition as the rover is approaching the Bagnold Dunes?

    NASA Astrophysics Data System (ADS)

    Cousin, Agnès; Forni, Olivier; Meslin, Pierre-Yves; Schroeder, Susanne; Gasnault, Olivier; Bridges, Nathan; Ehlmann, Bethany; Maurice, Sylvestre; Wiens, Roger

    2016-04-01

    The ChemCam instrument has the capability to study the chemical composition of soils at a sub-millimeter scale, thus providing an unpreceedented spatial resolution for their study. More than 300 soils have been sampled so far with ChemCam and these targets are analyzed frequently in order to monitor any change in composition along the traverse. Detailed chemical analysis as a function of grain size is of great importance in order to better constrain soils formation. Curiosity is approaching the Bagnold Dunes, the first active dune field accessible for in-situ analyses. One of the main goals is to determine or constrain the dune material chemistry as well as its provenance. This study is focusing on recent soils analyzed when ap-proaching the dunes, for a comparison with previous soil targets, and with dunes specifically. Chemical composition of fine-grained soils as we approach the Bagnold Dunes has been compared with previous fine-grained soils analyzed along the traverse. These new soils have an average sum of oxides that is significantly higher than what has been previously analyzed. This would suggest that these soils are less hydrated and probably less altered than previous ones.An enrichment in SiO2, FeO and alkali is also observed in these new fine-grained soils, which could be related to a contamination by local rocks due to erosion. Some coarser grains could correspond to an olivine component. This analysis is on-going and will be detailed as the dedicated Bagnold Dunes campaign starts. We will also report in the hydratation level of the dunes.

  19. Boron carbide: Consistency of components, lattice parameters, fine structure and chemical composition makes the complex structure reasonable

    NASA Astrophysics Data System (ADS)

    Werheit, Helmut

    2016-10-01

    The complex, highly distorted structure of boron carbide is composed of B12 and B11C icosahedra and CBC, CBB and B□B linear elements, whose concentration depends on the chemical composition each. These concentrations are shown to be consistent with lattice parameters, fine structure data and chemical composition. The respective impacts on lattice parameters are estimated and discussed. Considering the contributions of the different structural components to the energy of the overall structure makes the structure and its variation within the homogeneity range reasonable; in particular that of B4.3C representing the carbon-rich limit of the homogeneity range. Replacing in B4.3C virtually the B□B components by CBC yields the hypothetical moderately distorted B4.0C (structure formula (B11C)CBC). The reduction of lattice parameters related is compatible with recently reported uncommonly prepared single crystals, whose compositions deviate from B4.3C.

  20. Ambient fine particulate concentrations and chemical composition at two sampling sites in metropolitan Pittsburgh: a 2001 intensive summer study

    NASA Astrophysics Data System (ADS)

    Modey, William K.; Eatough, Delbert J.; Anderson, Richard R.; Martello, Donald V.; Takahama, Satoshi; Lucas, Leonard J.; Davidson, Cliff I.

    The concentration and chemical composition of ambient fine particulate material (PM 2.5) is reported for two sampling sites in the Pittsburgh, Pennsylvania metropolitan area: the Department of Energy, National Energy Technology Laboratory (NETL) PM study site south of the city center, and the Carnegie Mellon Pittsburgh Air Quality Study (PAQS) site 5 km east of central Pittsburgh established with funding by the EPA Supersites Program and by DOE-NETL. Data from these sampling sites were characterized by one to three-day episodes with PM 2.5 concentrations (constructed from the sum of the chemical components) exceeding 40.0 μg m -3. The episodes were dominated by high concentrations of ammonium sulfate. The fine particle concentrations were compared with meteorological data from surface weather maps and a Hybrid Single Particle Lagrangian Integrated Trajectory model (HYSPLIT model), with back-trajectories estimated over 24 h. High PM 2.5 concentrations were associated with transition from a high pressure to a low pressure regime in advance of an approaching frontal system indicating long-range transport of pollutants. In contrast, fine particulate organic material appeared to be dominated by nearby sources. Distinct differences were observed in the diurnal variations in concentration between the two sites. The NETL site showed clear maximum concentrations of semi-volatile organic material (SVOM) during midday, and minimum concentrations of nonvolatile organic compounds in the afternoon. In contrast, the Carnegie Mellon PAQS site showed an absence of diurnal variation in SVOM, but still with minimum concentrations of nonvolatile organic compounds in the afternoon and evening. Neither site showed significant diurnal variation in ammonium sulfate.

  1. Evaporation Rates of Chemical Warfare Agents Using 5 cm Wind Tunnels, IV. VX From Glass

    DTIC Science & Technology

    2010-06-01

    splitless injection port at 250 °C. The split vent was turned on at 0.5 min with a purge flow of 50 mL/min of helium. Retention times were I min for...EDGEWOOD CHEMICAL BIOLOGICAL CENTER U.S. ARMY RESEARCH. DEVELOPMENT AND ENGINEERING COMMAND ECBC-TR-777 EVAPORATION RATES OF CHEMICAL WARFARE...function of environmental conditions. 15. SUBJECT TERMS VX Glass Evaporation rate Wind tunnc 16. SECURITY CLASSIFICATION OF: a. REPORT u b. ABSTRACT

  2. ESCA studies of the surface chemistry of lunar fines. [Electron Spectroscopic Chemical Analysis

    NASA Technical Reports Server (NTRS)

    Housley, R. M.; Grant, R. W.

    1976-01-01

    The paper presents an ESCA analysis based on the use of a synthetic lunar-glass standard that allows determination of the surface composition of lunar samples with an accuracy that appears to be better than 10% of the amount present for all major elements except Ti. It is found that, on the average, grain surfaces in the lunar fines samples 10084 and 15301 are strongly enriched in Si, moderately enriched in Fe, moderately depleted in Al and Ca, and strongly depleted in Mg. This pattern could not be produced by the deposition of any expected meteoritic vapor. Neither could it be produced by simple inverse-mass-dependent element loss during sputtering. It is suggested that at least part of the pattern may be a simple consequence of agglutinate glass formation in the fines since there is some evidence that Si can become enriched on the surface of silicate melts. These results do not support the strong enrichments in Fe on grain surfaces reported from Auger studies.

  3. ESCA studies of the surface chemistry of lunar fines. [Electron Spectroscopic Chemical Analysis

    NASA Technical Reports Server (NTRS)

    Housley, R. M.; Grant, R. W.

    1976-01-01

    The paper presents an ESCA analysis based on the use of a synthetic lunar-glass standard that allows determination of the surface composition of lunar samples with an accuracy that appears to be better than 10% of the amount present for all major elements except Ti. It is found that, on the average, grain surfaces in the lunar fines samples 10084 and 15301 are strongly enriched in Si, moderately enriched in Fe, moderately depleted in Al and Ca, and strongly depleted in Mg. This pattern could not be produced by the deposition of any expected meteoritic vapor. Neither could it be produced by simple inverse-mass-dependent element loss during sputtering. It is suggested that at least part of the pattern may be a simple consequence of agglutinate glass formation in the fines since there is some evidence that Si can become enriched on the surface of silicate melts. These results do not support the strong enrichments in Fe on grain surfaces reported from Auger studies.

  4. Chemicals identified in human biological media, a data base. Interim report, May 1982 Volume IV

    SciTech Connect

    Cone, M.V.; Baldauf, M.F.; Opresko, D.M.; Uziel, M.S.

    1982-05-01

    A comprehensive data base of chemicals identified in human biological media has been established under the direction of the Exposure Evaluation Division in the US Environmental Protection Agency's Office of Toxic Substances. This centralized resource of body-burden information has grown out of the concern of government scientists over continuing reports of toxic chemicals in human tissues and body fluids. Body burden is a reflection of exposures to food, air, and water contaminants, as well as administration of pharmaceuticals. The systematic acquisition of body-burden data will facilitate a more relevant assessment of human exposure to xenobiotics than was previously possible using environmental contamination levels. Data were obtained primarily from the open literature (retrospective to 1974), and contains information on over 950 different substances. For the user's convenience, cross-referenced chemical lists of CAS preferred names and common names are provided. The human tissues and body fluids found to be contaminated by these chemicals are also listed. The data base is published annually in tabular format with indices and chemical listings that allow specific searching. The file is now available online in the US Department of Energy's RECON and is being prepared for Lockheed's DIALOG. The purpose of the data base is to provide a centralized resource of body-burden data.

  5. Phytophthora ramorum and sudden oak death in California: IV. preliminary studies on chemical control

    Treesearch

    Matteo Garbelotto; David M. Rizzo; Lawrence Marais

    2002-01-01

    Chemical applications may provide one means of control for Phytophthora ramorum, the cause of Sudden Oak Death (SOD). Such controls have been effective with other Phytophthora species in landscape and orchard situations. We have initiated laboratory and field studies to test the efficacy of a number of products previously reported...

  6. Computers in Chemical Education Newsletter. Volume IV Numbers 1-4.

    ERIC Educational Resources Information Center

    Rosenthal, Donald, Ed.

    1981-01-01

    Selections from volume 4 (numbers 1-4) of the Task Force on Computers in Chemical Education (TFCCE) Newsletter are presented. Number 1 includes an introduction to and objectives of the newsletter and TFCCE, a report on computer-related activities in the chemistry department at Eastern Michigan University, a list of TFCCE members, a discussion of a…

  7. Salmonella mutagenicity tests. IV. Results from the testing of 300 chemicals

    SciTech Connect

    Zeiger, E.; Anderson, B.; Haworth, S.; Lawlor, T.; Mortelmans, K.

    1988-01-01

    Three hundred chemicals were tested for mutagenicity, under code, in Salmonella typhimurium, using a preincubation protocol. All tests were performed in the absence of exogenous metabolic activation, and in the presence of liver S-9 from Aroclor-induced male Sprague-Dawley rats and Syrian hamsters. The results and data from these tests are presented.

  8. Chemistry in disks. IV. Benchmarking gas-grain chemical models with surface reactions

    NASA Astrophysics Data System (ADS)

    Semenov, D.; Hersant, F.; Wakelam, V.; Dutrey, A.; Chapillon, E.; Guilloteau, St.; Henning, Th.; Launhardt, R.; Piétu, V.; Schreyer, K.

    2010-11-01

    Context. We describe and benchmark two sophisticated chemical models developed by the Heidelberg and Bordeaux astrochemistry groups. Aims: The main goal of this study is to elaborate on a few well-described tests for state-of-the-art astrochemical codes covering a range of physical conditions and chemical processes, in particular those aimed at constraining current and future interferometric observations of protoplanetary disks. Methods: We considered three physical models: a cold molecular cloud core, a hot core, and an outer region of a T Tauri disk. Our chemical network (for both models) is based on the original gas-phase osu_03_2008 ratefile and includes gas-grain interactions and a set of surface reactions for the H-, O-, C-, S-, and N-bearing molecules. The benchmarking was performed with the increasing complexity of the considered processes: (1) the pure gas-phase chemistry, (2) the gas-phase chemistry with accretion and desorption, and (3) the full gas-grain model with surface reactions. The chemical evolution is modeled within 109 years using atomic initial abundances with heavily depleted metals and hydrogen in its molecular form. Results: The time-dependent abundances calculated with the two chemical models are essentially the same for all considered physical cases and for all species, including the most complex polyatomic ions and organic molecules. This result, however, required a lot of effort to make all necessary details consistent through the model runs, e.g., definition of the gas particle density, density of grain surface sites, or the strength and shape of the UV radiation field. Conclusions: The reference models and the benchmark setup, along with the two chemical codes and resulting time-dependent abundances are made publicly available on the internet. This will facilitate and ease the development of other astrochemical models and provide nonspecialists with a detailed description of the model ingredients and requirements to analyze the cosmic

  9. Factors affecting the microbial and chemical composition of silage. IV. Effect of wilting on maize silage.

    PubMed

    Mahmoud, S A; Abdel-Hafez, A; Zaki, M M; Saleh, E A

    1979-01-01

    The effect of wilting on the microbial and chemical composition of ensiled maize plants was studied. Wilting stimulated high densities of lactic acid bacteria, with the decrease in counts of undesirable flora, i.e., yeasts, moulds, proteolytic and saccharolytic anaerobes, causing spoilage of silage. Moreover, wilting decreased the losses of dry matter, total acidity, and butyric acid content of silage. Accordingly, wilting proved to be a favourable treatment for the production of good quality silage from maize plants.

  10. Performance predictions for solar-chemical converters based on photoelectrochemical I-V curves

    SciTech Connect

    Luttmer, J.D.; Trachtenberg, I.

    1985-06-01

    Texas Instruments' solar energy system contains a solar-chemical converter (SCC) which converts solar energy into chemical energy via the electrolysis of hydrobromic acid (HBr) into hydrogen (H/sub 2/) and bromine (Br/sub 2/). Previous predictions of SCC performance have employed electrical dry-probe data and a computer simulation model to predict the H/sub 2/ generation rates. The method of prediction described here makes use of the photoelectrochemical Icurves to determine the ''wet'' probe parameters of V /SUB oc/ J /SUB sc/ FF, and efficiency for anodes and cathodes. The advantages of this technique over the dry-probe/computer simulation method are discussed. A comparison of predicted and measured H/sub 2/ generation rates is presented. Solar to chemical efficiencies of 8.6% have been both predicted and measured for the electrolysis of 48% HBr to hydrogen and bromine by a full anode/cathode array. Individual cathode solar to hydrogen efficiencies of 9.5% have been obtained.

  11. Toxicity of chemical components of fine particles inhaled by aged rats: effects of concentration.

    PubMed

    Kleinman, Michael T; Hyde, Dallas M; Bufalino, Charles; Basbaum, Carol; Bhalla, Deepak K; Mautz, William J

    2003-09-01

    This study tested the hypothesis that exposure to mixtures containing fine particles and ozone (O3) would cause pulmonary injury and decrements in functions of immunological cells in exposed rats (22-24 months old) in a dose-dependent manner. Rats were exposed to high and low concentrations of ammonium bisulfate and elemental carbon and to 0.2 ppm O3. Control groups were exposed to purified air or O3 alone. The biological end points measured included histopathological markers of lung injury, bronchoalveolar lung fluid proteins, and measures of the function of the lung's innate immunological defenses (macrophage antigen-directed phagocytosis and respiratory burst activity). Exposure to O3 alone at 0.2 ppm did not result in significant changes in any of the measured end points. Exposures to the particle mixtures plus O3 produced statistically significant changes consistent with adverse effects. The low-concentration mixture produced effects that were statistically significant compared to purified air but, with the exception of macrophage Fc receptor binding, exposure to the high-concentration mixture did not. The effects of the low- and high-concentration mixtures were not significantly different. The study supports previous work that indicated that particle + O3 mixtures were more toxic than O3 alone.

  12. ATSDR evaluation of health effects of chemicals. IV. Polycyclic aromatic hydrocarbons (PAHs): understanding a complex problem.

    PubMed

    Mumtaz, M M; George, J D; Gold, K W; Cibulas, W; DeRosa, C T

    1996-01-01

    Polycyclic Aromatic Hydrocarbons (PAHs) are a group of chemicals that are formed during the incomplete burning of coal, oil, gas, wood, garbage, or other organic substances, such as tobacco and charbroiled meat. There are more than 100 PAHs. PAHs generally occur as complex mixtures (for example, as part of products such as soot), not as single compounds. PAHs are found throughout the environment in the air, water, and soil. As part of its mandate, the Agency for Toxic Substances and Disease Registry (ATSDR) prepares toxicological profiles on hazardous chemicals, including PAHs (ATSDR, 1995), found at facilities on the Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA) National Priorities List (NPL) and which pose the most significant potential threat to human health, as determined by ATSDR and the Environmental Protection Agency (EPA). These profiles include information on health effects of chemicals from different routes and durations of exposure, their potential for exposure, regulations and advisories, and the adequacy of the existing database. Assessing the health effects of PAHs is a major challenge because environmental exposures to these chemicals are usually to complex mixtures of PAHs with other chemicals. The biological consequences of human exposure to mixtures of PAHs depend on the toxicity, carcinogenic and noncarcinogenic, of the individual components of the mixture, the types of interactions among them, and confounding factors that are not thoroughly understood. Also identified are components of exposure and health effects research needed on PAHs that will allow estimation of realistic human health risks posed by exposures to PAHs. The exposure assessment component of research should focus on (1) development of reliable analytical methods for the determination of bioavailable PAHs following ingestion, (2) estimation of bioavailable PAHs from environmental media, particularly the determination of particle-bound PAHs, (3

  13. Chemical composition of crystalline rock fragments from Luna 16 and Luna 20 fines

    NASA Technical Reports Server (NTRS)

    Cimbalnikova, A.; Palivcova, M.; Frana, J.; Mastalka, A.

    1977-01-01

    The chemical composition (bulk, rare earth, and trace elements) of the Luna 16 mare regolith and luna 20 highland regolith is discussed. The rock samples considered are 14 basaltic rock fragments (Luna 16) and 13 rock fragments of the ANT suite (Luna 20). On the basis of bulk composition, two types of basaltic rocks have been differentiated and defined in the Luna 16 regolith: mare basalts (fundamental crystalline rocks of Mare Fecunditatis) and high-alumina basalts. The bulk analyses of rock fragments of the ANT suite also enabled distinction of two rock types: anorthositic norites and troctolites and/or spinal-troctolites (the most abundant crystalline rocks of the highland region, the landing site of luna 20), and anorthosites. The chemical compositions of Luna 16 and Luna 20 regolith samples are compared. Differences in the chemistry of the Luna 16 mare regolith and that of mare basalts are discussed. The chemical affinity between the Luna 20 highland regolith and (a) anorthositic norites and (b) troctolites and/or spinel-troctolites has been ascertained.

  14. Dissolution of cerium(IV)-lanthanide(III) oxides: Comparative effect of chemical composition, temperature, and acidity

    SciTech Connect

    Horlait, D.; Clavier, N.; Szenknect, S.; Dacheux, N.; Dubois, V.

    2012-03-15

    The dissolution of Ce{sub 1-x}Ln{sub x}O{sub 2-x/2} solid solutions was undertaken in various acid media in order to evaluate the effects of several physicochemical parameters such as chemical composition, temperature, and acidity on the reaction kinetics. The normalized dissolution rates (R{sub L,0}) were found to be strongly modified by the trivalent lanthanide incorporation rate, due to the presence of oxygen vacancies decreasing the samples cohesion. Conversely, the nature of the trivalent cation considered only weakly impacted the R{sub L,0} values. The dependence of the normalized dissolution rates on the temperature then appeared to be of the same order of magnitude than that of chemical composition. Moreover, it allowed determining the corresponding activation energy (E{sub A} ≅ 60-85 kJ.mol{sup -1}) which accounts for a dissolution driven by surface-controlled reactions. A similar conclusion was made regarding the acidity of the solution: the partial order related to (H{sub 3}O{sup +}) reaching about 0.7. Finally, the prevailing effect of the incorporation of aliovalent cations in the fluorite-type CeO{sub 2} matrix on the dissolution kinetics precluded the observation of slight effects such as those linked to the complexing agents or to the crystal structure of the samples. (authors)

  15. Analyses of fine paste ceramics

    SciTech Connect

    Sabloff, J A

    1980-01-01

    Four chapters are included: history of Brookhaven fine paste ceramics project, chemical and mathematical procedures employed in Mayan fine paste ceramics project, and compositional and archaeological perspectives on the Mayan fine paste ceramics. (DLC)

  16. Sources and Chemical Composition of Atmospheric Fine Particles in Rabigh, Saudi Arabia

    NASA Astrophysics Data System (ADS)

    Nayebare, S. R.; Aburizaiza, O. S.; Siddique, A.; Hussain, M. M.; Zeb, J.; Khwaja, H. A.

    2014-12-01

    Air pollution research in Saudi Arabia and the whole of Middle East is at its inception, making air pollution in the region a significant problem. This study presents the first detailed data on fine particulate matter (PM2.5) concentrations of Black Carbon (BC), ions, and trace metals at Rabigh, Saudi Arabia, and assesses their sources. Results showed several characteristic aspects of air pollution at Rabigh. Daily levels of PM2.5 and BC showed significant temporal variability ranging from 12.2 - 75.9 µg/m3 and 0.39 - 1.31 µg/m3, respectively. More than 90% of the time, the daily PM2.5 exceeded the 24 h WHO guideline of 20 µg/m3. Sulfate, NO3-, and NH4+ dominated the identifiable components. Trace metals with significantly higher concentrations included Si, S, Ca, Al, Fe, Na, Cl, Mg, K, and Ti, with average concentrations of 3.1, 2.2, 1.6, 1.2, 1.1, 0.7, 0.7, 0.5, 0.4 and 0.1 µg/m3, respectively. Based on the Air Quality Index (AQI), there were 44% days of moderate air quality, 33% days of unhealthy air quality for sensitive groups, and 23% days of unhealthy air quality throughout the study period. Two categories of aerosol trace metal sources were defined: anthropogenic (S, V, Cr, Ni, Cu, Zn, Br, Cd, Sb, and Pb) and naturally derived elements (Si, Al, and Fe). The extent of anthropogenic contribution was estimated by the degree of enrichment of these elements compared to the crustal composition. Soil resuspension and/or mobilization is an important source of "natural" elements, while "anthropogenic" elements originate primarily from fossil fuel combustion and industries. Ni and V correlated strongly pointing to combustion of heavy fuel oil as the likely source. A positive matrix factorization (PMF) was used to obtain information about possible sources. Our study highlights the need for stringent laws on PM2.5 emission control to protect human health and the environment.

  17. Clarifying the chemical state of additives in membranes for polymer electrolyte fuel cells by X-ray absorption fine structure

    NASA Astrophysics Data System (ADS)

    Tanuma, Toshihiro; Itoh, Takanori

    2016-02-01

    Cerium and manganese compounds are used in the membrane for polymer electrolyte fuel cells (PEFCs) as radical scavengers to mitigate chemical degradation of the membrane. The chemical states of cerium and manganese in the membrane were investigated using a fluorescence X-ray absorption fine structure (XAFS) technique. Membrane electrode assemblies (MEAs) were subjected to open circuit voltage (OCV) condition, under which hydroxyl radicals attack the membrane; a shift in absorption energy in X-ray absorption near edge structure (XANES) spectra was compared between Ce- and Mn-containing membranes before and after OCV testing. In the case of the Ce-containing MEA, there was no significant difference in XANES spectra before and after OCV testing, whereas in the case of the Mn-containing MEA, there was an obvious shift in XANES absorption energy after OCV testing, indicating that Mn atoms with higher valence state than 2+ exist in the membrane after OCV testing. This can be attributed to the difference in the rate of reduction; the reaction of Ce4+ with ·OOH is much faster than that of Mn3+ with ·OOH, leaving some of the Mn atoms with higher valence state. It was confirmed that cerium and manganese redox couples reduced the attack from radicals, mitigating membrane degradation.

  18. Mercury Speciation by X-ray Absorption Fine Structure Spectroscopy and Sequential Chemical Extractions: A Comparison of Speciation Methods

    USGS Publications Warehouse

    Kim, C.S.; Bloom, N.S.; Rytuba, J.J.; Brown, Gordon E.

    2003-01-01

    Determining the chemical speciation of mercury in contaminated mining and industrial environments is essential for predicting its solubility, transport behavior, and potential bioavailability as well as for designing effective remediation strategies. In this study, two techniques for determining Hg speciation-X-ray absorption fine structure (XAFS) spectroscopy and sequential chemical extractions (SCE)-are independently applied to a set of samples with Hg concentrations ranging from 132 to 7539 mg/kg to determine if the two techniques provide comparable Hg speciation results. Generally, the proportions of insoluble HgS (cinnabar, metacinnabar) and HgSe identified by XAFS correlate well with the proportion of Hg removed in the aqua regia extraction demonstrated to remove HgS and HgSe. Statistically significant (> 10%) differences are observed however in samples containing more soluble Hg-containing phases (HgCl2, HgO, Hg3S2O 4). Such differences may be related to matrix, particle size, or crystallinity effects, which could affect the apparent solubility of Hg phases present. In more highly concentrated samples, microscopy techniques can help characterize the Hg-bearing species in complex multiphase natural samples.

  19. Child Development Associate Training Program. Unit IV: Motor Development in Young Children. Module 2: Fostering the Development of Fine Motor Skills in Young Children.

    ERIC Educational Resources Information Center

    Office of Child Development (DHEW), Washington, DC.

    Skills necessary for fostering fine motor development in young children are indicated and discussed in this training module for Child Development Associate (CDA) trainees. Trainees are taught to identify appropriate classroom equipment and materials, plan lessons and activities, assess children's skills, and finally teach a lesson or guide an…

  20. Integrated operation of continuous chromatography and biotransformations for the generic high yield production of fine chemicals.

    PubMed

    Bechtold, Matthias; Makart, Stefan; Heinemann, Matthias; Panke, Sven

    2006-06-25

    The rapid progress in biocatalysis in the identification and development of enzymes over the last decade has enormously enlarged the chemical reaction space that can be addressed not only in research applications, but also on industrial scale. This enables us to consider even those groups of reactions that are very promising from a synthetic point of view, but suffer from drawbacks on process level, such as an unfavourable position of the reaction equilibrium. Prominent examples stem from the aldolase-catalyzed enantioselective carbon-carbon bond forming reactions, reactions catalyzed by isomerising enzymes, and reactions that are kinetically controlled. On the other hand, continuous chromatography concepts such as the simulating moving bed technology have matured and are increasingly realized on industrial scale for the efficient separation of difficult compound mixtures - including enantiomers - with unprecedented efficiency. We propose that coupling of enzyme reactor and continuous chromatography is a very suitable and potentially generic process concept to address the thermodynamic limitations of a host of promising biotransformations. This way, it should be possible to establish novel in situ product recovery processes of unprecedented efficiency and selectivity that represent a feasible way to recruit novel biocatalysts to the industrial portfolio.

  1. Chemical characterization of indoor and outdoor fine particulate matter in an occupied apartment in Rome, Italy.

    PubMed

    Perrino, C; Tofful, L; Canepari, S

    2016-08-01

    The daily concentration and chemical composition of PM2.5 was determined in indoor and outdoor 24-h samples simultaneously collected for a total of 5 weeks during a winter and a summer period in an apartment sited in Rome, Italy. The use of a specifically developed very quiet sampler (<35 dB) allowed the execution of the study while the family living in the apartment led its normal life. The indoor concentration of PM2.5 showed a small seasonal variation, while outdoor values were much higher during the winter study. Outdoor sources were found to contribute significantly to indoor PM concentration especially during the summer, when the apartment was naturally ventilated by opening the windows. During the winter the infiltration of outdoor PM components was lower and mostly regulated by the particle dimensions. Organics displayed In/Out ratios higher than unity during both periods; their indoor production increased significantly during the weekends, where the family stayed mostly at home. PM components were grouped into macrosources (soil, sea, secondary inorganics, traffic, organics). During the summer the main contributions to outdoor PM2.5 came from soil (30%), secondary inorganics (29%) and organics (22%). Organics dominated both indoor PM2.5 during the summer (60%) and outdoor and indoor PM2.5 during the winter (51% and 66%, respectively). © 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

  2. Chemical compositions of fine particulate organic matter emitted from Chinese cooking.

    PubMed

    Zhao, Yunliang; Hu, Min; Slanina, Sjaak; Zhang, Yuanhang

    2007-01-01

    Food cooking can be a significant source of atmospheric particulate organic matter. In this study, the chemical composition of particulate organic matter (POM) in PM2.5 emitted from four different Chinese cooking styles were examined by gas chromotography-mass spectrometry (GC-MS). The identified species are consistent in the emissions from different Chinese cooking styles and the quantified compounds account for 5-10% of total POM in PM2.5. The dominant homologue is fatty acids, constituting 73-85% of the quantified compounds. The pattern of n-alkanes and the presence of beta-sitosterol and levoglucosan indicate that vegetables are consumed during Chinese cooking operations. Furthermore, the emissions of different compounds are impacted significantly by the cooking ingredients. The candidates of organic tracers used to describe and distinguish emissions from Chinese cooking in Guangzhou are tetradecanoic acid, hexadecanoic acid, octadecanoic acid, oleic acid, levoglucosan, mannosan, galactosan, nonanal, and lactones. During the sampling period, the relative contribution of Chinese cooking to the mass concentration of atmospheric hexadecanoic acid should be less than 1.3% in Guangzhou.

  3. The Nainital-Cape Survey. IV. A search for pulsational variability in 108 chemically peculiar stars

    NASA Astrophysics Data System (ADS)

    Joshi, S.; Martinez, P.; Chowdhury, S.; Chakradhari, N. K.; Joshi, Y. C.; van Heerden, P.; Medupe, T.; Kumar, Y. B.; Kuhn, R. B.

    2016-05-01

    Context. The Nainital-Cape Survey is a dedicated ongoing survey program to search for and study pulsational variability in chemically peculiar (CP) stars to understand their internal structure and evolution. Aims: The main aims of this survey are to find new pulsating Ap and Am stars in the northern and southern hemisphere and to perform asteroseismic studies of these new pulsators. Methods: The survey is conducted using high-speed photometry. The candidate stars were selected on the basis of having Strömgren photometric indices similar to those of known pulsating CP stars. Results: Over the last decade a total of 337 candidate pulsating CP stars were observed for the Nainital-Cape Survey, making it one of the longest ground-based surveys for pulsation in CP stars in terms of time span and sample size. The previous papers of this series presented seven new pulsating variables and 229 null results. In this paper we present the light curves, frequency spectra and various astrophysical parameters of the 108 additional CP stars observed since the last reported results. We also tabulated the basic physical parameters of the known roAp stars. As a part of establishing the detection limits in the Nainital-Cape Survey, we investigated the scintillation noise level at the two observing sites used in this survey, Sutherland and Nainital, by comparing the combined frequency spectra stars observed from each location. Our analysis shows that both the sites permit the detection of variations of the order of 0.6 milli-magnitude (mmag) in the frequency range 1-4 mHz, Sutherland is on average marginally better. The dataset is only available at the CDS via anonymous ftp to http://cdsarc.u-strasbg.fr (http://130.79.128.5) or via http://cdsarc.u-strasbg.fr/viz-bin/qcat?J/A+A/590/A116

  4. Chemical Composition and Emission Sources of the Fine Particulate Matters in a Southeast Asian Mega City (Dhaka, Bangladesh)

    NASA Astrophysics Data System (ADS)

    Salam, Abdus

    2016-04-01

    Air pollution has significant impact on human health, climate change, agriculture, visibility reduction, and also on the atmospheric chemistry. There are many studies already reported about the direct relation of the human mortality and morbidity with the increase of the atmospheric particulate matters. Especially, fine particulate matters can easily enter into the human respiratory system and causes many diseases. Particulate matters have the properties to absorb the solar radiation and impact on the climate. Dhaka, Bangladesh is a densely populated mega-city in the world. About 16 million inhabitants are living within an area of 360 square kilometers. Air quality situation has been degrading due to unplanned growth, increasing vehicles, severe traffic jams, brick kilns, industries, construction, and also transboundary air pollution. A rapidly growing number of vehicles has worsen the air quality in spite of major policy interventions, e.g., ban of two-stroke and three-wheeled vehicles, phase out of 20 years old vehicles, conversion to compressed natural gas (CNGs), etc. Introduction of CNGs to reduce air pollution was not the solution for fine particles at all, as evidence shows that CNGs and diesel engines are the major sources of fine particles. High concentration of the air pollutants in Dhaka city such as PM, carbonaceous species (black and organic carbon), CO, etc. has already been reported. PM2.5 mass, chemical composition (e.g., BC, OC, SO42-, NO3-, trace elements, etc.), aerosol Optical Depth (AOD) and emission sources of our recent measurements at the highly polluted south East Asian Mega city (Dhaka) Bangladesh will be presented in the conference. PM2.5 samples were collected on filters with Digital PM2.5 sampler (Switzerland) and Air photon, USA. BC was measured from filters (with thermal and optical method) and also real time with an Aethalometer AE42 (Magee Scitific., USA). Water soluble ions were determined from filters with ion chromatogram. AOD

  5. Chemical characterization of the fine particle emissions from commercial aircraft engines during the Aircraft Particle Emissions eXperiment (APEX) 1 to 3

    EPA Science Inventory

    This paper addresses the need for detailed chemical information on the fine particulate matter (PM2.5) generated by commercial aviation engines. The exhaust plumes of nine engine models were sampled during the three test campaigns of the Aircraft Particle Emissions eXperiment (AP...

  6. Chemical characterization of the fine particle emissions from commercial aircraft engines during the Aircraft Particle Emissions eXperiment (APEX) 1 to 3

    EPA Science Inventory

    This paper addresses the need for detailed chemical information on the fine particulate matter (PM2.5) generated by commercial aviation engines. The exhaust plumes of nine engine models were sampled during the three test campaigns of the Aircraft Particle Emissions eXperiment (AP...

  7. Micro-chemical and metallurgical study of Samnite bronze belts from ancient Abruzzo (central Italy, VIII-IV BC)

    NASA Astrophysics Data System (ADS)

    Riccucci, Cristina; Ingo, Gabriel Maria; Faustoferri, Amalia; Pierigè, Maria Isabella; Parisi, Erica Isabella; Di Carlo, Gabriella; De Caro, Tilde; Faraldi, Federica

    2013-12-01

    The Samnite bronze belts and the chest disk cuirasses (VIII-IV BC) are the distinctive defensive weapons of the Samnite warriors having likely also a symbolic relevance. These artefacts were mainly found during the archaeological excavations of warriors' graves from ancient Abruzzo (central Italy). Their chemical composition, metallurgical features and corrosion products formed during the long-term burial have been studied by means of the combined use of analytical techniques such as optical microscopy (OM), scanning electron microscopy coupled with energy-dispersive X-ray micro-analysis (SEM-EDS), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The micro-chemical and structural results show that the bronze belts have often been produced by using unusual high-tin bronze alloys achieving a silver-like appearance and by performing tailored cycles of thermal treatments under reducing conditions and hot mechanical working aimed to shape the high-tin alloys in the form of a thin bronze sheet. Furthermore, the investigation has shown that the main alloying elements have been transformed during the burial into mineral species giving rise to the formation of stratified structures constituted by different mineral phases such as tin oxides, cuprous oxide (Cu2O) and copper carbonates (azurite (Cu3(CO3)2(OH)2 and malachite (CuCO3Cu(OH)2)) as well as dangerous chlorine-based compounds such as nantokite (CuCl) and atacamite (Cu2(OH)3Cl) polymorphs. This information evidences the strict interaction of the alloying elements with the soil components as well as the occurrence of the copper cyclic corrosion as a post-burial degradation phenomenon. The present study confirms that the combined micro-chemical and micro-structural investigation techniques such as SEM-EDS, XPS, XRD and OM can be successfully used to investigate the technological production processes of the ancient artefacts and to achieve the detailed micro-chemical and structural description of the

  8. Chemical characteristics and source apportionment of indoor and outdoor fine particles observed in an urban environment in Korea

    NASA Astrophysics Data System (ADS)

    Heo, J.; Yi, S. M.

    2016-12-01

    Paired indoor-outdoor fine particulate matter (PM2.5) samples were collected at subway stations, underground shopping centers, and schools in Seoul metropolitan over a 4-year period between 2004 and 2007. Relationships between indoor and outdoor PM2.5 chemical species were determined and source contributions to indoor and outdoor PM2.5 mass were estimated using a positive matrix factorization (PMF) model. The PM2.5 samples were analyzed for major chemical components including organic carbon and elemental carbon, ions, and metals, and the results were used in the PMF model. The levels of the PM2.5 mass and its chemical components observed at the indoor sites were higher than those at the outdoor sites. Indoor levels of ions (i.e. sulfate, nitrate, ammonium), elemental carbon, and several metals (i.e. Fe, Zn, and Cu) were found to be significantly affected by outdoor sources. Very high indoor-to-outdoor mass ratio of these chemical components, in particular, were observed, representing the significant impacts of outdoor sources on indoor levels of them. Seven sources (secondary sulfate, secondary nitrate, mobile, biomass burning, roadway emissions, dust, and sea salt) were resolved by the PMF model at both of the indoor and outdoor sites. The secondary inorganic aerosol (i.e. secondary sulfate and nitrate) and the mobile sources were major contributors to the indoor and outdoor PM2.5, accounting for 47% and 27% of the outdoor PM2.5 and 40% and 25% of the indoor PM2.5, respectively. Furthermore, the contributions of the secondary inorganic aerosol and the mobile sources to the indoor PM2.5 were very comparable to its corresponding contributions to the outdoor PM2.5 levels. The spatial and temporal characteristics of each of sources resolved by the PMF model across the sites were examined using summary statistics, correlation analysis, and coefficient of variation and divergence analysis and the detailed results will be discussed in the presentation.

  9. Direct micellar systems as a tool to improve the efficiency of aromatic substrate conversion for fine chemicals production.

    PubMed

    Berti, D; Randazzo, D; Briganti, F; Baglioni, P; Scozzafava, A; Di Gennaro, P; Galli, E; Bestetti, G

    2000-04-01

    Whole-cell bioconversion of naphthalene to (+)-cis-(1R,2S)-dihydroxy-1,2-dihydronaphthalene by Escherichia coli JM109(pPS1778) recombinant strain, carrying naphthalene dioxygenase and regulatory genes cloned from Pseudomonas fluorescens N3, in direct micellar systems is optimized as an example of fine chemicals bioproduction from scarcely water-soluble substrates. The oxygen insertion into the aromatic substrate, which stops at the enantiomerically pure cis dihydroxylated product, is performed in direct microemulsion systems, where a non-ionic surfactant stabilizes naphthalene containing oil droplets in an aqueous medium. These media provide an increased substrate solubility so that a homogeneous reaction can be carried out, while not affecting bacteria viability and performances. The influence of the chemical nature of the oil is investigated. The phase behavior of the direct microemulsion system was monitored for three different oils as a function their volume fraction and characterized through light scattering. The addition of isopropyl palmitate, oleic acid, or glyceryl trioleate, 0.6-1.2% v/v to the micellar systems, led to an increase of the substrate concentration in the solution and particularly its bioavailability, allowing faster catalytic conversions. All these systems resulted in being suitable for catalytic conversions of aromatic compounds. Although the nature of the oil does have a deep effect on the phase behavior of the micellar systems, in the present investigation no differences in the yields and in the rates of product formation of the enzymatic system were observed on changing the oil, thus showing that in this case the substrate concentration or bioavailability is not the rate-limiting step.

  10. Enhanced benzaldehyde tolerance in Zymomonas mobilis biofilms and the potential of biofilm applications in fine-chemical production.

    PubMed

    Li, Xuan Zhong; Webb, Jeremy S; Kjelleberg, Staffan; Rosche, Bettina

    2006-02-01

    Biotransformation plays an increasingly important role in the industrial production of fine chemicals due to its high product specificity and low energy requirement. One challenge in biotransformation is the toxicity of substrates and/or products to biocatalytic microorganisms and enzymes. Biofilms are known for their enhanced tolerance of hostile environments compared to planktonic free-living cells. Zymomonas mobilis was used in this study as a model organism to examine the potential of surface-associated biofilms for biotransformation of chemicals into value-added products. Z. mobilis formed a biofilm with a complex three-dimensional architecture comprised of microcolonies with an average thickness of 20 microm, interspersed with water channels. Microscopic analysis and metabolic activity studies revealed that Z. mobilis biofilm cells were more tolerant to the toxic substrate benzaldehyde than planktonic cells were. When exposed to 50 mM benzaldehyde for 1 h, biofilm cells exhibited an average of 45% residual metabolic activity, while planktonic cells were completely inactivated. Three hours of exposure to 30 mM benzaldehyde resulted in sixfold-higher residual metabolic activity in biofilm cells than in planktonic cells. Cells inactivated by benzaldehyde were evenly distributed throughout the biofilm, indicating that the resistance mechanism was different from mass transfer limitation. We also found that enhanced tolerance to benzaldehyde was not due to the conversion of benzaldehyde into less toxic compounds. In the presence of glucose, Z. mobilis biofilms in continuous cultures transformed 10 mM benzaldehyde into benzyl alcohol at a steady rate of 8.11 g (g dry weight)(-1) day(-1) with a 90% molar yield over a 45-h production period.

  11. Intercomparison of an Aerosol Chemical Speciation Monitor (ACSM) with ambient fine aerosol measurements in downtown Atlanta, Georgia

    NASA Astrophysics Data System (ADS)

    Budisulistiorini, S. H.; Canagaratna, M. R.; Croteau, P. L.; Baumann, K.; Edgerton, E. S.; Kollman, M. S.; Ng, N. L.; Verma, V.; Shaw, S. L.; Knipping, E. M.; Worsnop, D. R.; Jayne, J. T.; Weber, R. J.; Surratt, J. D.

    2014-07-01

    Currently, there are a limited number of field studies that evaluate the long-term performance of the Aerodyne Aerosol Chemical Speciation Monitor (ACSM) against established monitoring networks. In this study, we present seasonal intercomparisons of the ACSM with collocated fine aerosol (PM2.5) measurements at the Southeastern Aerosol Research and Characterization (SEARCH) Jefferson Street (JST) site near downtown Atlanta, GA, during 2011-2012. Intercomparison of two collocated ACSMs resulted in strong correlations (r2 > 0.8) for all chemical species, except chloride (r2 = 0.21) indicating that ACSM instruments are capable of stable and reproducible operation. In general, speciated ACSM mass concentrations correlate well (r2 > 0.7) with the filter-adjusted continuous measurements from JST, although the correlation for nitrate is weaker (r2 = 0.55) in summer. Correlations of the ACSM NR-PM1 (non-refractory particulate matter with aerodynamic diameter less than or equal to 1 μm) plus elemental carbon (EC) with tapered element oscillating microbalance (TEOM) PM2.5 and Federal Reference Method (FRM) PM1 mass are strong with r2 > 0.7 and r2 > 0.8, respectively. Discrepancies might be attributed to evaporative losses of semi-volatile species from the filter measurements used to adjust the collocated continuous measurements. This suggests that adjusting the ambient aerosol continuous measurements with results from filter analysis introduced additional bias to the measurements. We also recommend to calibrate the ambient aerosol monitoring instruments using aerosol standards rather than gas-phase standards. The fitting approach for ACSM relative ionization for sulfate was shown to improve the comparisons between ACSM and collocated measurements in the absence of calibrated values, suggesting the importance of adding sulfate calibration into the ACSM calibration routine.

  12. Enhanced Benzaldehyde Tolerance in Zymomonas mobilis Biofilms and the Potential of Biofilm Applications in Fine-Chemical Production

    PubMed Central

    Li, Xuan Zhong; Webb, Jeremy S.; Kjelleberg, Staffan; Rosche, Bettina

    2006-01-01

    Biotransformation plays an increasingly important role in the industrial production of fine chemicals due to its high product specificity and low energy requirement. One challenge in biotransformation is the toxicity of substrates and/or products to biocatalytic microorganisms and enzymes. Biofilms are known for their enhanced tolerance of hostile environments compared to planktonic free-living cells. Zymomonas mobilis was used in this study as a model organism to examine the potential of surface-associated biofilms for biotransformation of chemicals into value-added products. Z. mobilis formed a biofilm with a complex three-dimensional architecture comprised of microcolonies with an average thickness of 20 μm, interspersed with water channels. Microscopic analysis and metabolic activity studies revealed that Z. mobilis biofilm cells were more tolerant to the toxic substrate benzaldehyde than planktonic cells were. When exposed to 50 mM benzaldehyde for 1 h, biofilm cells exhibited an average of 45% residual metabolic activity, while planktonic cells were completely inactivated. Three hours of exposure to 30 mM benzaldehyde resulted in sixfold-higher residual metabolic activity in biofilm cells than in planktonic cells. Cells inactivated by benzaldehyde were evenly distributed throughout the biofilm, indicating that the resistance mechanism was different from mass transfer limitation. We also found that enhanced tolerance to benzaldehyde was not due to the conversion of benzaldehyde into less toxic compounds. In the presence of glucose, Z. mobilis biofilms in continuous cultures transformed 10 mM benzaldehyde into benzyl alcohol at a steady rate of 8.11 g (g dry weight)−1 day−1 with a 90% molar yield over a 45-h production period. PMID:16461720

  13. Chemical composition of fine particles in fresh smoke plumes from boreal wild-land fires in Europe.

    PubMed

    Saarnio, Karri; Aurela, Minna; Timonen, Hilkka; Saarikoski, Sanna; Teinilä, Kimmo; Mäkelä, Timo; Sofiev, Mikhail; Koskinen, Jarkko; Aalto, Pasi P; Kulmala, Markku; Kukkonen, Jaakko; Hillamo, Risto

    2010-05-15

    A series of smoke plumes was detected in Helsinki, Finland, during a one-month-lasting period in August 2006. The smoke plumes originated from wildfires close to Finland, and they were short-term and had a high particulate matter (PM) concentration. Physical and chemical properties of fine particles in those smokes were characterised by a wide range of real-time measurements that enabled the examination of individual plume events. Concurrently PM(1) filter samples were collected and analysed off-line. Satellite observations employing MODIS sensor on board of NASA EOS Terra satellite with the dispersion model SILAM and the Fire Assimilation System were used for evaluation of the emission fluxes from wildfires. The model predicted well the timing of the plumes but the predicted PM concentrations differed from the observed. The measurements showed that the major growth in PM concentration was caused by submicrometer particles consisting mainly of particulate organic matter (POM). POM had not totally oxidised during the transport based on the low WSOC-to-OC ratio. The fresh plumes were compared to another major smoke episode that was observed in Helsinki during April-May 2006. The duration and the source areas of the two episode periods differed. The episode in April-May was a period of nearly constantly upraised level of long-range transported PM and it was composed of aged particles when arriving in Helsinki. The two episodes had differences also in the chemical composition of PM. The mass concentrations of biomass burning tracers (levoglucosan, potassium, and oxalate) increased during both the episodes but different concentration levels of elemental carbon and potassium indicated that the episodes differed in the form of burning as well as in the burning material. In spring dry crop residue and hay from the previous season were burnt whereas in August smokes from smouldering and incomplete burning of fresh vegetation were detected.

  14. Spatial and Temporal Variation in Fine Particulate Matter Mass and Chemical Composition: The Middle East Consortium for Aerosol Research Study

    PubMed Central

    Abdeen, Ziad; Heo, Jongbae; Wu, Bo; Shpund, Jacob; Vanger, Arye; Sharf, Geula; Moise, Tamar; Brenner, Shmuel; Nassar, Khaled; Saleh, Rami; Al-Mahasneh, Qusai M.; Sarnat, Jeremy A.; Schauer, James J.

    2014-01-01

    Ambient fine particulate matter (PM2.5) samples were collected from January to December 2007 to investigate the sources and chemical speciation in Palestine, Jordan, and Israel. The 24-h PM2.5 samples were collected on 6-day intervals at eleven urban and rural sites simultaneously. Major chemical components including metals, ions, and organic and elemental carbon were analyzed. The mass concentrations of PM2.5 across the 11 sites varied from 20.6 to 40.3 μg/m3, with an average of 28.7 μg/m3. Seasonal variation of PM2.5 concentrations was substantial, with higher average concentrations (37.3 μg/m3) in the summer (April–June) months compared to winter (October–December) months (26.0 μg/m3) due mainly to high contributions of sulfate and crustal components. PM2.5 concentrations in the spring were greatly impacted by regional dust storms. Carbonaceous mass was the most abundant component, contributing 40% to the total PM2.5 mass averaged across the eleven sites. Crustal components averaged 19.1% of the PM2.5 mass and sulfate, ammonium, and nitrate accounted for 16.2%, 6.4%, and 3.7%, respectively, of the total PM2.5 mass. The results of this study demonstrate the need to better protect the health and welfare of the residents on both sides of the Jordan River in the Middle East. PMID:25045751

  15. Spatial and temporal variation in fine particulate matter mass and chemical composition: the Middle East Consortium for Aerosol Research Study.

    PubMed

    Abdeen, Ziad; Qasrawi, Radwan; Heo, Jongbae; Wu, Bo; Shpund, Jacob; Vanger, Arye; Sharf, Geula; Moise, Tamar; Brenner, Shmuel; Nassar, Khaled; Saleh, Rami; Al-Mahasneh, Qusai M; Sarnat, Jeremy A; Schauer, James J

    2014-01-01

    Ambient fine particulate matter (PM2.5) samples were collected from January to December 2007 to investigate the sources and chemical speciation in Palestine, Jordan, and Israel. The 24-h PM2.5 samples were collected on 6-day intervals at eleven urban and rural sites simultaneously. Major chemical components including metals, ions, and organic and elemental carbon were analyzed. The mass concentrations of PM2.5 across the 11 sites varied from 20.6 to 40.3 μg/m(3), with an average of 28.7 μg/m(3). Seasonal variation of PM2.5 concentrations was substantial, with higher average concentrations (37.3 μg/m(3)) in the summer (April-June) months compared to winter (October-December) months (26.0 μg/m(3)) due mainly to high contributions of sulfate and crustal components. PM2.5 concentrations in the spring were greatly impacted by regional dust storms. Carbonaceous mass was the most abundant component, contributing 40% to the total PM2.5 mass averaged across the eleven sites. Crustal components averaged 19.1% of the PM2.5 mass and sulfate, ammonium, and nitrate accounted for 16.2%, 6.4%, and 3.7%, respectively, of the total PM2.5 mass. The results of this study demonstrate the need to better protect the health and welfare of the residents on both sides of the Jordan River in the Middle East.

  16. Zirconium(IV) tungstate nanoparticles prepared through chemical co-precipitation method and its function as solid acid catalyst

    NASA Astrophysics Data System (ADS)

    Sadanandan, Manoj; Bhaskaran, Beena

    2014-08-01

    In this paper, we report the synthesis of zirconium(IV) tungstate nanoparticles, a new and efficient catalyst for the oxidation of benzyl alcohol and esterification of acetic acid with various alcohols. The nanoparticle catalyst was prepared using the room temperature chemical co-precipitation method. The catalyst was characterized with thermogravimetric and differential thermal analysis, elemental analysis, X-ray diffraction analysis (XRD), fourier transform infrared spectroscopy (FT-IR), high-resolution transmission electron microscopy (HRTEM), atomic force microscopy (AFM) and the Brunauer-Emmett-Teller (BET) surface area. The crystallite size was found to be ~20 nm as revealed by XRD, HRTEM and AFM. The Na+ exchange capacity was found to be 2.76 meq g-1 and the surface area of the compound measured using BET method was found to be 250-265 m2 g-1. The high value of ion exchange capacity indicates the presence of surface hydroxyl groups. The prepared nanoparticles have proven to be excellent catalysts for both oxidation and ester synthesis under mild reaction conditions. The mechanism of the catalytic reaction was studied as well.

  17. Characterization of chemical components and bioreactivity of fine particulate matter (PM2.5) during incense burning.

    PubMed

    Lui, K H; Bandowe, Benjamin A Musa; Ho, Steven Sai Hang; Chuang, Hsiao-Chi; Cao, Jun-Ji; Chuang, Kai-Jen; Lee, S C; Hu, Di; Ho, K F

    2016-06-01

    The chemical and bioreactivity properties of fine particulate matter (PM2.5) emitted during controlled burning of different brands of incense were characterized. Incenses marketed as being environmentally friendly emitted lower mass of PM2.5 particulates than did traditional incenses. However, the environmentally friendly incenses produced higher total concentrations of non-volatile polycyclic aromatic hydrocarbons (PAHs) and some oxygenated polycyclic aromatic hydrocarbons (OPAHs). Human alveolar epithelial A549 cells were exposed to the collected PM2.5, followed by determining oxidative stress and inflammation. There was moderate to strong positive correlation (R > 0.60, p < 0.05) between selected PAHs and OPAHs against oxidative-inflammatory responses. Strong positive correlation was observed between interleukin 6 (IL-6) and summation of total Group B2 PAHs/OPAHs (∑7PAHs/ΣOPAHs). The experimental data indicate that emissions from the environmentally friendly incenses contained higher concentrations of several PAH and OPAH compounds than did traditional incense. Moreover, these PAHs and OPAHs were strongly correlated with inflammatory responses. The findings suggest a need to revise existing regulation of such products.

  18. Anionic Extraction for Efficient Recovery of Biobased 2,3-Butanediol-A Platform for Bulk and Fine Chemicals.

    PubMed

    Drabo, Peter; Tiso, Till; Heyman, Benedikt; Sarikaya, Eda; Gaspar, Paula; Förster, Jochen; Büchs, Jochen; Blank, Lars Mathias; Delidovich, Irina

    2017-08-24

    2,3-Butanediol (BDO) presents a promising platform molecule for the synthesis of basic and fine chemicals. Biotechnological production of BDO from renewable resources with living microbes enables high concentrations in the fermentation broth. The recovery of high-boiling BDO from an aqueous fermentation broth presents a subsequent challenge. A method is proposed for BDO isolation based on reversible complexation with phenylboronate in an anionic complex. BDO can be recovered by back-extraction into an acidic solution. The composition of the extracted species was determined by NMR spectroscopy, MS, and GC-MS methods. The conditions of extraction and back-extraction were optimized by using commercial BDO and finally applied to different fermentation broths. Up to 72-93 % BDO can be extracted and up to 80-90 % can be back-extracted under the optimized conditions. Purified bio-BDO was used in the presence of sulfuric acid for the synthesis of methyl ethyl ketone, an established organic solvent and discussed tailor-made biofuel. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. Chemical characterization and sources of personal exposure to fine particulate matter in the general population of Guangzhou, China

    NASA Astrophysics Data System (ADS)

    Chen, Xiao-Cui; Jahn, Heiko J.; Engling, Guenter; Ward, Tony J.; Kraemer, Alexander; Ho, Kin-Fai; Hung-Lam Yim, Steve; Chan, Chuen-Yu

    2017-04-01

    Fine particulate matter pollution severely deteriorates the environmental conditions and negatively impacts human health in the Chinese megacity Guangzhou. Concurrent ambient and personal measurements of fine particulate matter (PM2.5) were conducted in Guangzhou, China. Personal-to-ambient (P-C) relationships of PM2.5 chemical components were determined and sources of personal PM2.5 exposure were evaluated using principal component analysis along with a mixed-effects model. Water-soluble inorganic ions (mainly secondary inorganic ions) and anhydrosugars exhibited median personal-to-ambient (P/C) ratios < 1 accompanied by strong P-C correlations, indicating that these constituents in personal PM2.5 were significantly affected by ambient sources. Conversely, elemental carbon (EC) and calcium (Ca2+) showed median P/C ratios greater than unity, which indicated that among subjects who spent a great amount of time indoors, aside from particles of ambient origin, individual's total exposure to PM2.5 includes contributions of non-ambient exposure while indoors and outdoors (e.g., local traffic, indoor sources, personal activities). SO42- displayed very low coefficient of divergence (COD) values coupled with strong P-C correlations, implying a uniform distribution of SO42- in the urban area of Guangzhou. EC, Ca2+, and levoglucosan were otherwise heterogeneously distributed across individuals in different districts. Regional air pollution (50.4 ± 0.9%), traffic-related particles (8.6 ± 0.7%), dust-related particles (5.8 ± 0.7%), and biomass burning emissions (2.0 ± 0.2%) were moderate to high positive sources of personal PM2.5 exposure in Guangzhou. The observed positive and significant contribution of Ca2+ to personal PM2.5 exposure, highlighting indoor sources and/or personal activities, were driving factors determining personal exposure to dust-related particles. Considerable discrepancies (COD values ranging from 0.42 to 0.50) were shown between ambient

  20. Fine and coarse particulate matter chemical characterization in a heavily industrialized city in central Mexico during Winter 2003.

    PubMed

    Vega, Elizabeth; Ruiz, Hugo; Martínez-Villa, Gerardo; Sosa, Gustavo; González-Avalos, Eugenio; Reyes, Elizabeth; García, José

    2007-05-01

    This paper presents the results of the first reported study on fine particulate matter (PM) chemical composition at Salamanca, a highly industrialized urban area of Central Mexico. Samples were collected at six sites within the urban area during February and March 2003. Several trace elements, organic carbon (OC), elemental carbon (EC), and six ions were analyzed to characterize aerosols. Average concentrations of PM with aerodynamic diameter of less than 10 microm (PM10) and fine PM with aerodynamic diameter of less than 2.5 microm (PM2.5) ranged from 32.2 to 76.6 [g m(-3) and 11.1 to 23.7 microg m(-3), respectively. OC (34%), SO4= (25.1%), EC (12.9%), and geological material (12.5%) were the major components of PM2.5. For PM10 geological material (57.9%), OC (17.3%), and SO4= (9.7%) were the major components. Coarse fraction (PM,, -PM2.5), geological material (81.7%), and OC (8.6%) were the dominant species, which amounted to 90.4%. Correlation analysis showed that sulfate in PM2.5 was present as ammonium sulfate. Sulfate showed a significant spatial variation with higher concentrations to the north resulting from predominantly southwesterly winds above the surface layer and by major SO2 sources that include a power plant and refinery. At the urban site of Cruz Roja it was observed that PM2.5 mass concentrations were similar to the submicron fraction concentrations. Furthermore, the correlation between EC in PM2.5 and EC measured from an aethalometer was r(2) = 0.710. Temporal variations of SO2 and nitrogen oxide were observed during a day when the maximum concentration of PM2.5 was measured, which was associated with emissions from the nearby refinery and power plant. From cascade impactor measurements, the three measured modes of airborne particles corresponded with diameters of 0.32, 1.8, and 5.6 microm.

  1. Physico-chemical properties of the new generation IV iron preparations ferumoxytol, iron isomaltoside 1000 and ferric carboxymaltose.

    PubMed

    Neiser, Susann; Rentsch, Daniel; Dippon, Urs; Kappler, Andreas; Weidler, Peter G; Göttlicher, Jörg; Steininger, Ralph; Wilhelm, Maria; Braitsch, Michaela; Funk, Felix; Philipp, Erik; Burckhardt, Susanna

    2015-08-01

    The advantage of the new generation IV iron preparations ferric carboxymaltose (FCM), ferumoxytol (FMX), and iron isomaltoside 1000 (IIM) is that they can be administered in relatively high doses in a short period of time. We investigated the physico-chemical properties of these preparations and compared them with those of the older preparations iron sucrose (IS), sodium ferric gluconate (SFG), and low molecular weight iron dextran (LMWID). Mössbauer spectroscopy, X-ray diffraction, and Fe K-edge X-ray absorption near edge structure spectroscopy indicated akaganeite structures (β-FeOOH) for the cores of FCM, IIM and IS, and a maghemite (γ-Fe2O3) structure for that of FMX. Nuclear magnetic resonance studies confirmed the structure of the carbohydrate of FMX as a reduced, carboxymethylated, low molecular weight dextran, and that of IIM as a reduced Dextran 1000. Polarography yielded significantly different fingerprints of the investigated compounds. Reductive degradation kinetics of FMX was faster than that of FCM and IIM, which is in contrast to the high stability of FMX towards acid degradation. The labile iron content, i.e. the amount of iron that is only weakly bound in the polynuclear iron core, was assessed by a qualitative test that confirmed decreasing labile iron contents in the order SFG ≈ IS > LMWID ≥ FMX ≈ IIM ≈ FCM. The presented data are a step forward in the characterization of these non-biological complex drugs, which is a prerequisite to understand their cellular uptake mechanisms and the relationship between the structure and physiological safety as well as efficacy of these complexes.

  2. New insight into the electronic structure of iron(IV)-oxo porphyrin compound I. A quantum chemical topological analysis.

    PubMed

    Viciano, Ignacio; Berski, Slawomir; Martí, Sergio; Andrés, Juan

    2013-04-05

    The electronic structure of iron-oxo porphyrin π-cation radical complex Por(·+) Fe(IV)=O (S-H) has been studied for doublet and quartet electronic states by means of two methods of the quantum chemical topology analysis: electron localization function (ELF) η(r) and electron density ρ(r). The formation of this complex leads to essential perturbation of the topological structure of the carbon-carbon bonds in porphyrin moiety. The double C=C bonds in the pyrrole anion subunits, represented by pair of bonding disynaptic basins V(i=1,2)(C,C) in isolated porphyrin, are replaced by single attractor V(C,C)(i=1-20) after complexation with the Fe cation. The iron-nitrogen bonds are covalent dative bonds, N→Fe, described by the disynaptic bonding basins V(Fe,N)(i=1-4), where electron density is almost formed by the lone pairs of the N atoms. The nature of the iron-oxygen bond predicted by the ELF topological analysis, shows a main contribution of the electrostatic interaction, Fe(δ+)···O(δ-), as long as no attractors between the C(Fe) and C(O) core basins were found, although there are common surfaces between the iron and oxygen basines and coupling between iron and oxygen lone pairs, that could be interpreted as a charge-shift bond. The Fe-S bond, characterized by the disynaptic bonding basin V(Fe,S), is partially a dative bond with the lone pair donated from sulfur atom. The change of electronic state from the doublet (M = 2) to quartet (M = 4) leads to reorganization of spin polarization, which is observed only for the porphyrin skeleton (-0.43e to 0.50e) and S-H bond (-0.55e to 0.52e).

  3. Chemical mass transport between fluid fine tailings and the overlying water cover of an oil sands end pit lake

    NASA Astrophysics Data System (ADS)

    Dompierre, Kathryn A.; Barbour, S. Lee; North, Rebecca L.; Carey, Sean K.; Lindsay, Matthew B. J.

    2017-06-01

    Fluid fine tailings (FFT) are a principal by-product of the bitumen extraction process at oil sands mines. Base Mine Lake (BML)—the first full-scale demonstration oil sands end pit lake (EPL)—contains approximately 1.9 × 108 m3 of FFT stored under a water cover within a decommissioned mine pit. Chemical mass transfer from the FFT to the water cover can occur via two key processes: (1) advection-dispersion driven by tailings settlement; and (2) FFT disturbance due to fluid movement in the water cover. Dissolved chloride (Cl) was used to evaluate the water cover mass balance and to track mass transport within the underlying FFT based on field sampling and numerical modeling. Results indicated that FFT was the dominant Cl source to the water cover and that the FFT is exhibiting a transient advection-dispersion mass transport regime with intermittent disturbance near the FFT-water interface. The advective pore water flux was estimated by the mass balance to be 0.002 m3 m-2 d-1, which represents 0.73 m of FFT settlement per year. However, the FFT pore water Cl concentrations and corresponding mass transport simulations indicated that advection rates and disturbance depths vary between sample locations. The disturbance depth was estimated to vary with location between 0.75 and 0.95 m. This investigation provides valuable insight for assessing the geochemical evolution of the water cover and performance of EPLs as an oil sands reclamation strategy.

  4. Fine particulate matter source apportionment for the Chemical speciation Trends Network site at Birmingham, Alabama, using Positive Matrix Factorization.

    PubMed

    Baumann, Karsten; Jayanty, R K M; Flanagan, James B

    2008-01-01

    The Positive Matrix Factorization (PMF) receptor model version 1.1 was used with data from the fine particulate matter (PM2.5) Chemical Speciation Trends Network (STN) to estimate source contributions to ambient PM2.5 in a highly industrialized urban setting in the southeastern United States. Model results consistently resolved 10 factors that are interpreted as two secondary, five industrial, one motor vehicle, one road dust, and one biomass burning sources. The STN dataset is generally not corrected for field blank levels, which are significant in the case of organic carbon (OC). Estimation of primary OC using the elemental carbon (EC) tracer method applied on a seasonal basis significantly improved the model's performance. Uniform increase of input data uncertainty and exclusion of a few outlier samples (associated with high potassium) further improved the model results. However, it was found that most PMF factors did not cleanly represent single source types and instead are "contaminated" by other sources, a situation that might be improved by controlling rotational ambiguity within the model. Secondary particulate matter formed by atmospheric processes, such as sulfate and secondary OC, contribute the majority of ambient PM2.5 and exhibit strong seasonality (37 +/- 10% winter vs. 55 +/- 16% summer average). Motor vehicle emissions constitute the biggest primary PM2.5 mass contribution with almost 25 +/- 2% long-term average and winter maximum of 29 +/- 11%. PM2.5 contributions from the five identified industrial sources vary little with season and average 14 +/- 1.3%. In summary, this study demonstrates the utility of the EC tracer method to effectively blank-correct the OC concentrations in the STN dataset. In addition, examination of the effect of input uncertainty estimates on model results indicates that the estimated uncertainties currently being provided with the STN data may be somewhat lower than the levels needed for optimum modeling results.

  5. Characterization of chemical composition and concentration of fine particulate matter during a transit strike in Ottawa, Canada

    NASA Astrophysics Data System (ADS)

    Ding, Luyi; Chan, Tak Wai; Ke, Fu; Wang, Daniel K. W.

    2014-06-01

    From December 10, 2008 to February 9, 2009, a strike stopped the public transit services in Ottawa, Ontario, Canada. To understand the changes in air quality associated with the transit strike, the chemical composition and concentration of the fine particulate matter with diameters less than 2.5 microns (PM2.5), collected before, during, and after the transit strike period, were evaluated. The collected PM2.5 samples were analyzed to determine the particulate matter mass, the levels of organic carbon (OC) and elemental carbon (EC), as well as the particulate non-polar semi-volatiles, e.g., polycyclic aromatic hydrocarbons (PAHs), hopanes, and steranes. Particle number size distributions measured during and after the transit strike period were also compared. Results indicated that during transit strike months, particle number size distributions were entirely dominated by nucleation mode particles leading to an increase in total particle number concentration by about 79%. In addition, particulate matter, organic carbon, and elemental carbon mass concentrations also increased by over 100%. The average total PAH levels during the strike months were higher by a factor of about 7. Elevated concentrations of high molecular weight PAHs (i.e., PAH with 5 and 6 rings) observed during the strike months suggested that there were more gasoline-powered vehicles on the roads over that period. The level of carcinogenic benzo[a]pyrene was higher by a factor of 5. Mass concentrations of hopanes and steranes were 30-98% higher during the strike months than non-strike months and exhibited strong correlations with EC suggesting the primary origin of these compounds. These results indicated that the increased traffic volume due to the passenger vehicles and the change in driving pattern during the transit strike period reduced the local air quality.

  6. Intercomparison of an Aerosol Chemical Speciation Monitor (ACSM) with ambient fine aerosol measurements in Downtown Atlanta, Georgia

    NASA Astrophysics Data System (ADS)

    Budisulistiorini, S. H.; Canagaratna, M. R.; Croteau, P. L.; Baumann, K.; Edgerton, E. S.; Kollman, M. S.; Ng, N. L.; Verma, V.; Shaw, S. L.; Knipping, E. M.; Worsnop, D. R.; Jayne, J. T.; Weber, R. J.; Surratt, J. D.

    2013-12-01

    The Aerodyne Aerosol Chemical Speciation Monitor (ACSM) was recently developed to provide long-term real-time continuous measurements of ambient non-refractory (i.e., organic, sulfate, ammonium, nitrate, and chloride) submicron particulate matter (NR-PM1). Currently, there are a limited number of field studies that evaluate the long-term performance of the ACSM against established monitoring networks. In this study, we present seasonal intercomparisons of the ACSM with collocated fine aerosol (PM2.5) measurements at the Southeastern Aerosol Research and Characterization (SEARCH) Jefferson Street (JST) site near downtown Atlanta, GA, during 2011-2012. The collocated measurements included a second ACSM, continuous and integrated sulfate, nitrate, and ammonium measurements, as well as a semi-continuous Sunset organic carbon/elemental carbon (OC/EC) analyzer, continuous tapered element oscillating microbalance (TEOM), 24 h integrated Federal Reference Method (FRM) filters, and continuous scanning electrical mobility system-mixing condensation particle counter (SEMS-MCPC). Intercomparison of the two collocated ACSMs resulted in strong correlations (r2 > 0.8) for all chemical species, except chloride (r2 = 0.21); mass concentration for all chemical species agreed within ±27%, indicating that ACSM instruments are capable of stable and reproducible operation. Chemical constituents measured by the ACSM are also compared with those obtained from the continuous measurements from JST. Since the continuous measurement concentrations are adjusted to match the integrated filter measurements, these comparisons reflect the combined uncertainties of the ACSM, continuous, and filter measurements. In general, speciated ACSM mass concentrations correlate well (r2 > 0.7) with the continuous measurements from JST, although the correlation for nitrate is weaker (r2 = 0.55) in summer. Differences between ACSM mass concentrations and the filter-adjusted JST continuous data are 5-27%, 4

  7. Pelletization of fine coals. Final report

    SciTech Connect

    Sastry, K.V.S.

    1995-12-31

    Coal is one of the most abundant energy resources in the US with nearly 800 million tons of it being mined annually. Process and environmental demands for low-ash, low-sulfur coals and economic constraints for high productivity are leading the coal industry to use such modern mining methods as longwall mining and such newer coal processing techniques as froth flotation, oil agglomeration, chemical cleaning and synthetic fuel production. All these processes are faced with one common problem area--fine coals. Dealing effectively with these fine coals during handling, storage, transportation, and/or processing continues to be a challenge facing the industry. Agglomeration by the unit operation of pelletization consists of tumbling moist fines in drums or discs. Past experimental work and limited commercial practice have shown that pelletization can alleviate the problems associated with fine coals. However, it was recognized that there exists a serious need for delineating the fundamental principles of fine coal pelletization. Accordingly, a research program has been carried involving four specific topics: (i) experimental investigation of coal pelletization kinetics, (ii) understanding the surface principles of coal pelletization, (iii) modeling of coal pelletization processes, and (iv) simulation of fine coal pelletization circuits. This report summarizes the major findings and provides relevant details of the research effort.

  8. Size distribution of chemical elements and their source apportionment in ambient coarse, fine, and ultrafine particles in Shanghai urban summer atmosphere.

    PubMed

    Lü, Senlin; Zhang, Rui; Yao, Zhenkun; Yi, Fei; Ren, Jingjing; Wu, Minghong; Feng, Man; Wang, Qingyue

    2012-01-01

    Ambient coarse particles (diameter 1.8-10 microm), fine particles (diameter 0.1-1.8 microm), and ultrafine particles (diameter < 0.1 microm) in the atmosphere of the city of Shanghai were sampled during the summer of 2008 (from Aug 27 to Sep 08). Microscopic characterization of the particles was investigated by scanning electron microscopy coupled with energy dispersive X-ray spectroscopy (SEM/EDX). Mass concentrations of Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, As, Se, Br, Rb, Sr, and Pb in the size-resolved particles were quantified by using synchrotron radiation X-ray fluorescence (SRXRF). Source apportionment of the chemical elements was analyzed by means of an enrichment factor method. Our results showed that the average mass concentrations of coarse particles, fine particles and ultrafine particles in the summer air were 9.38 +/- 2.18, 8.82 +/- 3.52, and 2.02 +/- 0.41 microg/m3, respectively. The mass percentage of the fine particles accounted for 51.47% in the total mass of PM10, indicating that fine particles are the major component in the Shanghai ambient particles. SEM/EDX results showed that the coarse particles were dominated by minerals, fine particles by soot aggregates and fly ashes, and ultrafine particles by soot particles and unidentified particles. SRXRF results demonstrated that crustal elements were mainly distributed in the coarse particles, while heavy metals were in higher proportions in the fine particles. Source apportionment revealed that Si, K, Ca, Fe, Mn, Rb, and Sr were from crustal sources, and S, Cl, Cu, Zn, As, Se, Br, and Pb from anthropogenic sources. Levels of P, V, Cr, and Ni in particles might be contributed from multi-sources, and need further investigation.

  9. Nontoxic chemical process for in situ permeability enhancement and accelerated decontamination of fine-grain subsurface sediments

    DOEpatents

    Kansa, Edward J.; Wijesinghe, Ananda M.; Viani, Brian E.

    1997-01-01

    The remediation of heterogeneous subsurfaces is extremely time consuming and expensive with current and developing technologies. Although such technologies can adequately remove contaminants in the high hydraulic conductivity, coarse-grained sediments, they cannot access the contaminated low hydraulic conductivity fine-grained sediments. The slow bleed of contaminants from the fine-grained sediments is the primary reason why subsurface remediation is so time-consuming and expensive. This invention addresses the problem of remediating contaminated fine-grained sediments. It is intended that, in the future, a heterogeneous site be treated by a hybrid process that first remediates the high hydraulic conductivity, coarse-grained sediments, to be followed by the process, described in this invention, to treat the contaminated low hydraulic conductivity fine-grained sediments. The invention uses cationic flocculents and organic solvents to collapse the swelling negative double layer surrounding water saturated clay particles, causing a flocculated, cracked clay structure. The modification of the clay fabric in fine-grained sediments dramatically increases the hydraulic conductivity of previously very tight clays many orders of magnitude.

  10. Nontoxic chemical process for in situ permeability enhancement and accelerated decontamination of fine-grain subsurface sediments

    DOEpatents

    Kansa, E.J.; Wijesinghe, A.M.; Viani, B.E.

    1997-01-14

    The remediation of heterogeneous subsurfaces is extremely time consuming and expensive with current and developing technologies. Although such technologies can adequately remove contaminants in the high hydraulic conductivity, coarse-grained sediments, they cannot access the contaminated low hydraulic conductivity fine-grained sediments. The slow bleed of contaminants from the fine-grained sediments is the primary reason why subsurface remediation is so time-consuming and expensive. This invention addresses the problem of remediating contaminated fine-grained sediments. It is intended that, in the future, a heterogeneous site be treated by a hybrid process that first remediates the high hydraulic conductivity, coarse-grained sediments, to be followed by the process, described in this invention, to treat the contaminated low hydraulic conductivity fine-grained sediments. The invention uses cationic flocculants and organic solvents to collapse the swelling negative double layer surrounding water saturated clay particles, causing a flocculated, cracked clay structure. The modification of the clay fabric in fine-grained sediments dramatically increases the hydraulic conductivity of previously very tight clays many orders of magnitude. 8 figs.

  11. Chemical characterization of fine particulate matter in Changzhou, China, and source apportionment with offline aerosol mass spectrometry

    NASA Astrophysics Data System (ADS)

    Ye, Zhaolian; Liu, Jiashu; Gu, Aijun; Feng, Feifei; Liu, Yuhai; Bi, Chenglu; Xu, Jianzhong; Li, Ling; Chen, Hui; Chen, Yanfang; Dai, Liang; Zhou, Quanfa; Ge, Xinlei

    2017-02-01

    Knowledge of aerosol chemistry in densely populated regions is critical for effective reduction of air pollution, while such studies have not been conducted in Changzhou, an important manufacturing base and populated city in the Yangtze River Delta (YRD), China. This work, for the first time, performed a thorough chemical characterization on the fine particulate matter (PM2.5) samples, collected during July 2015 to April 2016 across four seasons in this city. A suite of analytical techniques was employed to measure the organic carbon (OC), elemental carbon (EC), water-soluble organic carbon (WSOC), water-soluble inorganic ions (WSIIs), trace elements, and polycyclic aromatic hydrocarbons (PAHs) in PM2.5; in particular, an Aerodyne soot particle aerosol mass spectrometer (SP-AMS) was deployed to probe the chemical properties of water-soluble organic aerosol (WSOA). The average PM2.5 concentration was found to be 108.3 µg m-3, and all identified species were able to reconstruct ˜ 80 % of the PM2.5 mass. The WSIIs occupied about half of the PM2.5 mass (˜ 52.1 %), with SO42-, NO3-, and NH4+ as the major ions. On average, nitrate concentrations dominated over sulfate (mass ratio of 1.21), indicating that traffic emissions were more important than stationary sources. OC and EC correlated well with each other and the highest OC / EC ratio (5.16) occurred in winter, suggesting complex OC sources likely including both secondary and primary ones. Concentrations of eight trace elements (Mn, Zn, Al, B, Cr, Cu, Fe, Pb) can contribute up to ˜ 5.0 % of PM2.5 during winter. PAH concentrations were also high in winter (140.25 ng m-3), which were predominated by median/high molecular weight PAHs with five and six rings. The organic matter including both water-soluble and water-insoluble species occupied ˜ 21.5 % of the PM2.5 mass. SP-AMS determined that the WSOA had average atomic oxygen-to-carbon (O / C), hydrogen-to-carbon (H / C), nitrogen-to-carbon (N / C), and organic

  12. DEVELOPMENT AND EVALUATION OF A HIGH-VOLUME DICHOTOMOUS SAMPLER FOR CHEMICAL SPECIATION OF COARSE AND FINE PARTICLES

    EPA Science Inventory

    This paper describes the development and field evaluation of a compact high-volume dichotomous sampler (HVDS) that collects coarse (PM10-2.5) and fine (PM2.5) particulate matter. In its primary configuration as tested, the sampler size-fractionates PM10 into...

  13. DEVELOPMENT AND EVALUATION OF A HIGH-VOLUME DICHOTOMOUS SAMPLER FOR CHEMICAL SPECIATION OF COARSE AND FINE PARTICLES

    EPA Science Inventory

    This paper describes the development and field evaluation of a compact high-volume dichotomous sampler (HVDS) that collects coarse (PM10-2.5) and fine (PM2.5) particulate matter. In its primary configuration as tested, the sampler size-fractionates PM10 into...

  14. Organo- and nano-catalyst in greener reaction medium: Microwave-assisted expedient synthesis of fine chemicals

    EPA Science Inventory

    The use of emerging microwave (MW) -assisted chemistry techniques is dramatically reducing chemical waste and reaction times in several organic syntheses and chemical transformations. A brief account of our experiences in developing MW-assisted organic transformations, which invo...

  15. Update on the Chemical Composition Of Crystalline, Smectite, and Amorphous Components for Rocknest Soil and John Klein and Cumberland Mudstone Drill Fines at Gale Crater, Mars

    NASA Technical Reports Server (NTRS)

    Morris, R. V.; Ming, D. W.; Gellert, R.; Vaniman, D. T.; Bish, D. L.; Blake, D. F.; Chipera, S. J.; Morrison, S. M.; Downs, R. T.; Rampe, E. B.; Treiman, A. H.; Yen, A. S.; Achilles, C. N.; Archer, P. D.; Bristow, T. F.; Cavanaugh, P.; Fenrdrich, K.; Crisp, J. A.; Des Marais, D. J.; Farmer, J. D.; Grotzinger, J. P.; Mahaffy, P. R.; McAdam, A. C.; Morookian, J. M.

    2015-01-01

    We have previously calculated the chemical compositions of the X-ray-diffraction (XRD) amorphous component of three solid samples (Rocknest (RN) soil, John Klein (JK) drill fines, and Cumberland (CB) drill fines) using major-element chemistry (APXS), volatile-element chemistry (SAM), and crystalline- phase mineralogy (CheMin) obtained by the Curiosity rover as a part of the ongoing Mars Science Laboratory mission in Gale Crater. According to CheMin analysis, the RN and the JK and CB samples are mineralogically distinct in that RN has no detectable clay minerals and both JK and CB have significant concentrations of high-Fe saponite. The chemical composition of the XRD amorphous component is the composition remaining after mathematical removal of the compositions of crystalline components, including phyllosilicates if present. Subsequent to, we have improved the unit cell parameters for Fe-forsterite, augite, and pigeonite, resulting in revised chemical compositions for the XRD-derived crystalline component (excluding clay minerals). We update here the calculated compositions of amorphous components using these revised mineral compositions.

  16. Source areas and chemical composition of fine particulate matter in the Pearl River Delta region of China

    NASA Astrophysics Data System (ADS)

    Hagler, G. S. W.; Bergin, M. H.; Salmon, L. G.; Yu, J. Z.; Wan, E. C. H.; Zheng, M.; Zeng, L. M.; Kiang, C. S.; Zhang, Y. H.; Lau, A. K. H.; Schauer, J. J.

    Fine particulate matter (PM 2.5) was measured for 4 months during 2002-2003 at seven sites located in the rapidly developing Pearl River Delta region of China, an area encompassing the major cities of Hong Kong, Shenzhen and Guangzhou. The 4-month average fine particulate matter concentration ranged from 37 to 71 μg m -3 in Guangdong province and from 29 to 34 μg m -3 in Hong Kong. Main constituents of fine particulate mass were organic compounds (24-35% by mass) and sulfate (21-32%). With sampling sites strategically located to monitor the regional air shed patterns and urban areas, specific source-related fine particulate species (sulfate, organic mass, elemental carbon, potassium and lead) and daily surface winds were analyzed to estimate influential source locations. The impact of transport was investigated by categorizing 13 (of 20 total) sampling days by prevailing wind direction (southerly, northerly or low wind-speed mixed flow). The vicinity of Guangzhou is determined to be a major source area influencing regional concentrations of PM 2.5, with levels observed to increase by 18-34 μg m -3 (accounting for 46-56% of resulting particulate levels) at sites immediately downwind of Guangzhou. The area near Guangzhou is also observed to heavily impact downwind concentrations of lead. Potassium levels, related to biomass burning, appear to be controlled by sources in the northern part of the Pearl River Delta, near rural Conghua and urban Guangzhou. Guangzhou appears to contribute 5-6 μg m -3 of sulfate to downwind locations. Guangzhou also stands out as a significant regional source of organic mass (OM), adding 8.5-14.5 μg m -3 to downwind concentrations. Elemental carbon is observed to be strongly influenced by local sources, with highest levels found in urban regions. In addition, it appears that sources outside of the Pearl River Delta contribute a significant fraction of overall fine particulate matter in Hong Kong and Guangdong province. This is evident

  17. Chromosomal aberrations and sister chromatid exchange tests in Chinese hamster ovary cells in vitro. IV. Results with 15 chemicals

    SciTech Connect

    Ivett, J.L.; Brown, B.M.; Rodgers, C. ); Anderson, B.E.; Resnick, M.A.; Zeiger, E. )

    1989-01-01

    The National Toxicology Program has undertaken a study to assess the ability of four genetic toxicology assays to predict the carcinogenicity of chemicals in 2-year rodent studies. Two of the assays, used for evaluating in vitro cytogenic damage, were the SCE and chromosome aberration assays in Chinese hamster ovary cells. The results and data for 15 of the chemicals tested in these two assays are presented here. Each chemical was tested with and without exogenous metabolic activation. The chemicals tested were bisphenol A, 2-chloroethanol, C.l. acid orange 10, C.l. disperse yellow 3, C.l. solvent yellow 14, cytembena, D C red 9, 1,2-dibromoethane, FD C yellow 6, malaoxon, D,L-methanol, phenol, sulfisoxazole, titanium dioxide, and tris(2-ethyl-hexyl)phosphate. In vitro cytogenetic results from the other chemicals presented by Tennant et al. have been published by Galloway et al, Gulati et al. and Loveday et. al.

  18. Influence of thallium(I) and thallium(III) on parameters of oscillating chemical reaction in a bromate-cerium(III,IV)-malonic acid-sulfuric acid system

    SciTech Connect

    Yatsimirskii, K.B.; Matyushov, D.V.; Tikhonova, L.P.

    1987-06-01

    The influence of thallium(I) and thallium(III) on the parameters of the Belousov-Zhabotinskii oscillating chemical reaction in the bromate-cerium-(III, IV)-malonic acid-sulfuric acid system was studied. As a result of the addition of thallium(I) and thallium(III), the oscillation parameters change in the same way, which cannot be explained by the complexation of these ions with the bromide only. It was found that during the oscillating reaction, thallium(I) can be oxidized by bromine-containing compounds and thallium(III) reduced by the transformation products of malonic and bromomalonic acids. A scheme of action of a thallium(III)/thallium(I) two-electron redox pair in the oscillating chemical reaction studied has been proposed.

  19. Insight into chemical speciation based on solvent physical parameters: Illustration study using octahedral Pt(IV) complexes in several organic media

    NASA Astrophysics Data System (ADS)

    Jansat, Susanna

    2017-10-01

    Empirical dependence of Solvent Physical Parameters (SPhP) in front of the chemical shift for one proton signal (1H NMR) allows for, the understanding and prediction, of structural mer and fac isomer/s present in solution on, the chemical speciation originated by [PtBr(Tol)2(C,Nimino,Namino)] (Ardbnd CH3C6H4) in several solvents. Case illustrates how SPhP might be, valuable single data tools, dealing with speciation influenced by media. Hildebrand Parameter is the finest value to describe even rotoisomers for the more challenging athermal solutions. In function of media permittivity, more polar speciation is stabilized by the continuum media's polarity (ε) or, by specific dipole-solvent interactions (Solvent Dipolarity). Procedure has been applied for similar Pt(IV) compounds without uncertainty including multicomponent media.

  20. WATEQF; a FORTRAN IV version of WATEQ : a computer program for calculating chemical equilibrium of natural waters

    USGS Publications Warehouse

    Plummer, L. Niel; Jones, Blair F.; Truesdell, Alfred Hemingway

    1976-01-01

    WATEQF is a FORTRAN IV computer program that models the thermodynamic speciation of inorganic ions and complex species in solution for a given water analysis. The original version (WATEQ) was written in 1973 by A. H. Truesdell and B. F. Jones in Programming Language/one (PL/1.) With but a few exceptions, the thermochemical data, speciation, coefficients, and general calculation procedure of WATEQF is identical to the PL/1 version. This report notes the differences between WATEQF and WATEQ, demonstrates how to set up the input data to execute WATEQF, provides a test case for comparison, and makes available a listing of WATEQF. (Woodard-USGS)

  1. Chemical chaperone treatment reduces intracellular accumulation of mutant collagen IV and ameliorates the cellular phenotype of a COL4A2 mutation that causes haemorrhagic stroke.

    PubMed

    Murray, Lydia S; Lu, Yinhui; Taggart, Aislynn; Van Regemorter, Nicole; Vilain, Catheline; Abramowicz, Marc; Kadler, Karl E; Van Agtmael, Tom

    2014-01-15

    Haemorrhagic stroke accounts for ∼20% of stroke cases and porencephaly is a clinical consequence of perinatal cerebral haemorrhaging. Here, we report the identification of a novel dominant G702D mutation in the collagen domain of COL4A2 (collagen IV alpha chain 2) in a family displaying porencephaly with reduced penetrance. COL4A2 is the obligatory protein partner of COL4A1 but in contrast to most COL4A1 mutations, the COL4A2 mutation does not lead to eye or kidney disease. Analysis of dermal biopsies from a patient and his unaffected father, who also carries the mutation, revealed that both display basement membrane (BM) defects. Intriguingly, defective collagen IV incorporation into the dermal BM was observed in the patient only and was associated with endoplasmic reticulum (ER) retention of COL4A2 in primary dermal fibroblasts. This intracellular accumulation led to ER stress, unfolded protein response activation, reduced cell proliferation and increased apoptosis. Interestingly, the absence of ER retention of COL4A2 and ER stress in cells from the unaffected father indicate that accumulation and/or clearance of mutant COL4A2 from the ER may be a critical modifier for disease development. Our analysis also revealed that mutant collagen IV is degraded via the proteasome. Importantly, treatment of patient cells with a chemical chaperone decreased intracellular COL4A2 levels, ER stress and apoptosis, demonstrating that reducing intracellular collagen accumulation can ameliorate the cellular phenotype of COL4A2 mutations. Importantly, these data highlight that manipulation of chaperone levels, intracellular collagen accumulation and ER stress are potential therapeutic options for collagen IV diseases including haemorrhagic stroke.

  2. Inter-comparison of Seasonal Variation, Chemical Characteristics, and Source Identification of Atmospheric Fine Particles on Both Sides of the Taiwan Strait

    PubMed Central

    Li, Tsung-Chang; Yuan, Chung-Shin; Huang, Hu-Ching; Lee, Chon-Lin; Wu, Shui-Ping; Tong, Chuan

    2016-01-01

    The spatiotemporal distribution and chemical composition of atmospheric fine particles in areas around the Taiwan Strait were firstly investigated. Fine particles (PM2.5) were simultaneously collected at two sites on the west-side, one site at an offshore island, and three sites on the east-side of the Taiwan Strait in 2013–2014. Field sampling results indicated that the average PM2.5 concentrations at the west-side sampling sites were generally higher than those at the east-side sampling sites. In terms of chemical composition, the most abundant water-soluble ionic species of PM2.5 were SO42−, NO3−, and NH4+, while natural crustal elements dominated the metallic content of PM2.5, and the most abundant anthropogenic metals of PM2.5 were Pb, Ni and Zn. Moreover, high OC/EC ratios of PM2.5 were commonly observed at the west-side sampling sites, which are located at the downwind of major stationary sources. Results from CMB receptor modeling showed that the major sources of PM2.5 were anthropogenic sources and secondary aerosols at the both sides, and natural sources dominated PM2.5 at the offshore site. A consistent decrease of secondary sulfate and nitrate contribution to PM2.5 suggested the transportation of aged particles from the west-side to the east-side of the Taiwan Strait. PMID:26973085

  3. Exploration of DNA binding mode, chemical nuclease, cytotoxic and apoptotic potentials of diketone based oxovanadium(IV) complexes.

    PubMed

    Inamdar, Poonam Rajiv; Sheela, Angappan

    2015-05-01

    Two diketone based oxovanadium complexes, viz., bis(4,4,4-trifluoro-1-phenylbutane-1,3-dionato)oxovanadium(IV) (1) and bis(1,1,1-trifluoropentane-2,4-dionato)oxovanadium(IV) (2), have been synthesized and characterized by spectroscopic and analytical techniques. The DNA binding and the cleaving ability of the complexes is assessed by UV-vis spectroscopy, fluorescence spectroscopy, viscometry and gel electrophoretic studies. The DNA binding constant values (Kb) are found to be 1.95 ± 0.16 × 10(3)M(-1) for complex 1 and 1.064 ± 0.17 × 10(3)M(-1) for complex 2, respectively. Based on the results of the spectral and viscosity studies, it is observed that the complexes, interestingly, have preferred minor groove binding with DNA. Further, the concentration-dependent oxidative cleavage pattern of pBR322 in the presence of the activating reagent, hydrogen peroxide, has also been discussed. In addition, the complexes have shown moderate cytotoxic activity by inducing apoptosis against the cervical cancer cell line, HeLa. The results of in silico analysis and logP predictions are found to be in good agreement with the experimental observations. Thus, synthesized oxovanadium complexes have displayed promising DNA binding behavior and DNA cleavage activity with moderately cytotoxic nature.

  4. Size distribution, chemical composition, and hygroscopicity of fine particles emitted from an oil-fired heating plant.

    PubMed

    Happonen, Matti; Mylläri, Fanni; Karjalainen, Panu; Frey, Anna; Saarikoski, Sanna; Carbone, Samara; Hillamo, Risto; Pirjola, Liisa; Häyrinen, Anna; Kytömäki, Jorma; Niemi, Jarkko V; Keskinen, Jorma; Rönkkö, Topi

    2013-12-17

    Heavy fuel oil (HFO) is a commonly used fuel in industrial heating and power generation and for large marine vessels. In this study, the fine particle emissions of a 47 MW oil-fired boiler were studied at 30 MW power and with three different fuels. The studied fuels were HFO, water emulsion of HFO, and water emulsion of HFO mixed with light fuel oil (LFO). With all the fuels, the boiler emitted considerable amounts of particles smaller than 200 nm in diameter. Further, these small particles were quite hygroscopic even as fresh and, in the case of HFO+LFO emulsion, the hygroscopic growth of the particles was dependent on particle size. The use of emulsions and the addition of LFO to the fuel had a reducing effect on the hygroscopic growth of particles. The use of emulsions lowered the sulfate content of the smallest particles but did not affect significantly the sulfate content of particles larger than 42 nm and, further, the addition of LFO considerably increased the black carbon content of particulate matter. The results indicate that even the fine particles emitted from HFO based combustion can have a significant effect on cloud formation, visibility, and air quality.

  5. Fine particle emissions in three different combustion conditions of a wood chip-fired appliance - Particulate physico-chemical properties and induced cell death

    NASA Astrophysics Data System (ADS)

    Leskinen, J.; Tissari, J.; Uski, O.; Virén, A.; Torvela, T.; Kaivosoja, T.; Lamberg, H.; Nuutinen, I.; Kettunen, T.; Joutsensaari, J.; Jalava, P. I.; Sippula, O.; Hirvonen, M.-R.; Jokiniemi, J.

    2014-04-01

    A biomass combustion reactor with a moving grate was utilised as a model system to produce three different combustion conditions corresponding to efficient, intermediate, and smouldering combustion. The efficient conditions (based on a CO level of approximately 7 mg MJ-1) corresponded to a modern pellet boiler. The intermediate conditions (CO level of approximately 300 mg MJ-1) corresponded to non-optimal settings in a continuously fired biomass combustion appliance. The smouldering conditions (CO level of approximately 2200 mg MJ-1) approached a batch combustion situation. The gaseous and particle emissions were characterised under each condition. Moreover, the ability of fine particles to cause cell death was determined using the particle emissions samples. The physico-chemical properties of the emitted particles and their toxicity were considerably different between the studied combustion conditions. In the efficient combustion, the emitted particles were small in size and large in number. The PM1 emission was low, and it was composed of ash species. In the intermediate and smouldering combustion, the PM1 emission was higher, and the particles were larger in size and smaller in number. In both of these conditions, there were high-emission peaks that produced a significant fraction of the emissions. The PAH emissions were the lowest in the efficient combustion. The smouldering combustion conditions produced the largest PAH emissions. In efficient combustion conditions, the emitted fine particles had the highest potential to cause cell death. This finding was most likely observed because these fine particles were mainly composed of inorganic ash species, and their relative contents of Zn were high. Thus, even the PM1 from optimal biomass combustion might cause health effects, but in these conditions, the particle emissions per energy unit produced were considerably lower.

  6. Chemical composition of submicron and fine particulate matter collected in Krakow, Poland. Consequences for the APARIC project.

    PubMed

    Samek, Lucyna; Furman, Leszek; Mikrut, Magdalena; Regiel-Futyra, Anna; Macyk, Wojciech; Stochel, Grażyna; van Eldik, Rudi

    2017-11-01

    Submicron particulate matter containing particles with an aerodynamic diameter ≤1 μm (PM1) are not monitored continuously by Environmental Protection Agencies around the World and are seldom studied. Numerous studies have indicated that people exposed to ultrafine (≤100 nm), submicron and fine particulate matter containing particles with an aerodynamic diameter ≤2.5 μm (PM2.5), can suffer from respiratory track diseases, cardiovascular, immunological or heart diseases and others. Inorganic pollutants containing redox active transition metals and small gaseous molecules, are involved in the generation of reactive oxygen and reactive nitrogen species. Inhalation of this kind of particles can affect immune-toxicity. Environmental pollution may aggravate the course of autoimmune diseases, in particular influence the mechanisms of the autoimmune system. Important factors that influence the toxicity of particulate matter, are particle size distribution, composition and concentration. This report deals with the composition of PM1 and PM2.5 fractions collected in Krakow, Poland. In spring 2015, the mean concentrations of PM1 and PM2.5 were 19 ± 14 and 27 ± 19 μg/m(3), respectively. The PM2.5 fraction contained approximately 70 ± 17% of submicron particulate matter. In spring 2016, the mean concentrations of PM1 and PM2.5 were 12 ± 5 and 22 ± 12 μg/m(3), respectively. The PM2.5 fraction contained approximately 60 ± 15% of submicron particulate matter. The concentrations of the elements Cl, K, Ca, Ti, Cr, Mn, Fe, Ni, Cu, Zn, Br, Rb, Sr and Pb in both fractions were determined by X-ray fluorescence spectrometry. Most of the analyzed metals had higher concentrations in the fine fraction than in the submicron one. Concentrations of V and As were below the detection limit in both fractions, whereas concentrations of Mn and Ca were below the detection limits in the PM1 fraction. The results are discussed in terms of the consequences they may have on

  7. First structural characterization of Pa(iv) in aqueous solution and quantum chemical investigations of the tetravalent actinides up to Bk(IV): the evidence of a curium break.

    PubMed

    Banik, Nidhu lal; Vallet, Valérie; Réal, Florent; Belmecheri, Réda Mohamed; Schimmelpfennig, Bernd; Rothe, Jörg; Marsac, Rémi; Lindqvist-Reis, Patric; Walther, Clemens; Denecke, Melissa A; Marquardt, Christian M

    2016-01-14

    More than a century after its discovery the structure of the Pa(4+) ion in acidic aqueous solution has been investigated for the first time experimentally and by quantum chemistry. The combined results of EXAFS data and quantum chemically optimized structures suggest that the Pa(4+) aqua ion has an average of nine water molecules in its first hydration sphere at a mean Pa-O distance of 2.43 Å. The data available for the early tetravalent actinide (An) elements from Th(4+) to Bk(4+) show that the An-O bonds have a pronounced electrostatic character, with bond distances following the same monotonic decreasing trend as the An(4+) ionic radii, with a decrease of the hydration number from nine to eight for the heaviest ions Cm(4+) and Bk(4+). Being the first open-shell tetravalent actinide, Pa(4+) features a coordination chemistry very similar to its successors. The electronic configuration of all open-shell systems corresponds to occupation of the valence 5f orbitals, without contribution from the 6d orbitals. Our results thus demonstrate that Pa(iv) resembles its early actinide neighbors.

  8. Petrographic characterization of Kentucky coals. Final report. Part IV. A petrographic and chemical model for the evolution of the Tradewater Formation coals in Western Kentucky

    SciTech Connect

    Graese, A.M.; Hower, J.C.; Ferm, J.C.

    1984-01-01

    A depositional model for the coals of the Tradewater Formation and associated rock units was constructed as a predictive device for the occurrence of economically important low sulfur coal. Twenty-one cores were examined and ninety-eight coal samples were analyzed for maceral, ash, and sulfur contents. These data were then analyzed to determine regional variation as well as vertical variation in single coal columns. Core data indicate that the majority of the Tradewater rocks consist of irregularly distributed, coarsening-upward, fine-grained detrital material which was deposited in shallow bodies of water. Minor fossiliferous shales and limestones suggest a marine influence. Less common coarse-grained, fining-upward sequences appear to be deposits of meandering channels. Like the detrital rocks, the coal seams are also irregularly distributed and exhibit variable petrographic and chemical properties reflecting changes in the Eh and pH of the coal swamp waters as well as detrital influx into the swamps. These swamps were relatively limited in extent and probably occupied the upper reaches of the tidal zone. The lack of significant stratigraphic and geographic trends in the regional data suggests that this mode of deposition was widespread and continued for a long period of time. 42 references, 19 figures, 9 tables.

  9. Chemical characteristics and source apportionment of fine particulate organic carbon in Hong Kong during high particulate matter episodes in winter 2003

    NASA Astrophysics Data System (ADS)

    Li, Yun-Chun; Yu, Jian Zhen; Ho, Steven Sai Hang; Schauer, James J.; Yuan, Zibing; Lau, Alexis K. H.; Louie, Peter K. K.

    2013-02-01

    PM2.5 samples were collected at six general stations and one roadside station in Hong Kong in two periods of high particulate matter (PM) in 2003 (27 October-4 November and 30 November-13 December). The highest PM2.5 reached 216 μg m- 3 during the first high PM period and 113 μg m- 3 during the second high PM period. Analysis of synoptic weather conditions identified individual sampling days under dominant influence of one of three types of air masses, that is, local, regional and long-range transported (LRT) air masses. Roadside samples were discussed separately due to heavy influences from vehicular emissions. This research examines source apportionment of fine organic carbon (OC) and contribution of secondary organic aerosol on high PM days under different synoptic conditions. Six primary OC (POC) sources (vehicle exhaust, biomass burning, cooking, cigarette smoke, vegetative detritus, and coal combustion) were identified on the basis of characteristic organic tracers. Individual POC source contributions were estimated using chemical mass balance model. In the roadside and the local samples, OC was dominated by the primary sources, accounting for more than 74% of OC. In the samples influenced by regional and LRT air masses, secondary OC (SOC), which was approximated to be the difference between the total measured OC and the apportioned POC, contributed more than 54% of fine OC. SOC was highly correlated with water-soluble organic carbon and sulfate, consistent with its secondary nature.

  10. Physical, chemical and biological controls of nutrient fluxes from fine-grained, organic-rich sediments in the Indian River Lagoon, Florida

    NASA Astrophysics Data System (ADS)

    Fox, A. L.; Trefry, J. H.; Trocine, R. P.; Fox, S. L.; Yan, Y.

    2016-02-01

    Releases and biogeochemical controls of dissolved nitrogen and phosphorus from fine-grained, organic-rich sediments in the Indian River Lagoon, Florida, were determined using (1) interstitial water chemistry, (2) laboratory incubations and experiments, and (3) in situ chambers. Fluxes of nitrogen, essentially all as ammonium ions, and phosphorus, essentially all as orthophosphate ions, averaged 2000 ± 1000 and 130 ± 90 µmol/m2/day, respectively. This internal recycling of ammonium and phosphate from fine-grained, organic-rich sediments that comprise at least 10% of the sediments throughout the northern lagoon total 300 metric tons/yr and 50 metric tons/yr, respectively, and were greater than external inputs to this system. Ammonium fluxes varied spatially in response to physical and chemical differences in sediment composition. Seasonal and experimental changes in temperature resulted in a >50% differences in fluxes of ammonium and phosphate. High fluxes of dissolved sulfide supported dense mats of sulfur-oxidizing bacteria that provided stability to an otherwise unconsolidated fluff layer; this negative feedback loop reduced the net flux of nitrogen and phosphorus into the overlying water.

  11. Chemical Speciation and Health Risk Assessment of Fine Particulate Bound Trace Metals Emitted from Ota Industrial Estate, Nigeria

    NASA Astrophysics Data System (ADS)

    Anake, Winifred U.; Ana, Godson R. E. E.; Williams, Akan B.; Fred-Ahmadu, Omowunmi H.; Benson, Nsikak U.

    2017-05-01

    In this study carcinogenic and non-carcinogenic health risk due to exposure to PM2.5-bound trace metals from an industrial area in Southwestern Nigeria was estimated. A four-step chemical sequential extraction procedure was employed for the chemical extraction of arsenic (As), cadmium (Cd), chromium (Cr) copper (Cu), manganese (Mn), nickel (Ni), and zinc (Zn). Samples were analyzed using inductively coupled plasma mass spectrometry (ICP-MS). Results reveal Cr and Cu as the most dominant exchangeable fraction metals, indicating possibility of their being readily soluble once PM2.5 is inhaled. Cd and Cr record the highest bioavailability index of 0.7. The cumulative lifetime cancer risks due to inhalation exposure for adults (4.25×10-2), children 1-6 years old (4.87×10-3), and children 6-18 years old (1.46×10-2) were found above Environmental Protection Agency’s acceptable range of 1×10-6 to 1×10-4. The hazard index values for all studied trace metals suggest significant potential for non-carcinogenic health risks to adults and children. The choice of chemical speciation as an essential tool in facilitating a better predictive insight on metal bioavailability and toxicity for immediate remediation action has been highlighted.

  12. On the use of LUDI to search the Fine Chemicals Directory for ligands of proteins of known three-dimensional structure

    NASA Astrophysics Data System (ADS)

    Böhm, Hans-Joachim

    1994-10-01

    It is shown that the computer program LUDI can be used to search large databases of three-dimensional structures for putative ligands of proteins with known 3D structure. As an example, a subset of ≈30 000 small molecules (with less than 40 atoms and 0-2 rotatable bonds) from the Fine Chemicals Directory has been used in the search for possible novel ligands for four different proteins (trypsin, streptavidin, purine nucleoside phosphorylase and HIV protease). For trypsin and streptavidin, known ligands or substructures of known ligands are retrieved as top-scoring hits. In addition, a number of new interesting structures are found in all considered cases. Therefore, the method holds promise to retrieve automatically protein ligands from a 3D database if the 3D structure of the target protein is known.

  13. Source apportionment of ambient fine particulate matter in Dearborn, Michigan, using hourly resolved PM chemical composition data.

    PubMed

    Pancras, Joseph Patrick; Landis, Matthew S; Norris, Gary A; Vedantham, Ram; Dvonch, J Timothy

    2013-03-15

    High time-resolution aerosol sampling was conducted for one month during July-August 2007 in Dearborn, MI, a non-attainment area for fine particulate matter (PM2.5) National Ambient Air Quality Standards (NAAQS). Measurements of more than 30 PM2.5 species were made using a suite of semi-continuous sampling and monitoring instruments. Dynamic variations in the sub-hourly concentrations of source 'marker' elements were observed when discrete plumes from local sources impacted the sampling site. Hourly averaged PM2.5 composition data for 639 samples were used to identify and apportion PM2.5 emission sources using the multivariate receptor modeling techniques EPA Positive Matrix Factorization (PMF) v4.2 and EPA Unmix v6.0. Source contribution estimates from PMF and Unmix were then evaluated using the Sustained Wind Instance Method (SWIM), which identified plausible source origins. Ten sources were identified by both PMF and Unmix: (1) secondary sulfate, (2) secondary nitrate characterized by a significant diurnal trend, (3) iron and steel production, (4) a potassium-rich factor attributable to iron/steel slag waste processing, (5) a cadmium-rich factor attributable to incineration, (6) an oil refinery characterized by La/Ce>1 specific to south wind, (7) oil combustion, (8) coal combustion, (9) motor vehicles, and (10) road dust enriched with organic carbon. While both models apportioned secondary sulfate, oil refinery, and oil combustion PM2.5 masses closely, the mobile and industrial source apportionments differed. Analyses were also carried out to help infer time-of-day variations in the contributions of local sources.

  14. Chemical constituents of fine particulate air pollution and pulmonary function in healthy adults: the Healthy Volunteer Natural Relocation study.

    PubMed

    Wu, Shaowei; Deng, Furong; Hao, Yu; Shima, Masayuki; Wang, Xin; Zheng, Chanjuan; Wei, Hongying; Lv, Haibo; Lu, Xiuling; Huang, Jing; Qin, Yu; Guo, Xinbiao

    2013-09-15

    The study examined the associations of 32 chemical constituents of particulate matter with an aerodynamic diameter ≤2.5 μm (PM₂.₅) with pulmonary function in a panel of 21 college students. Study subjects relocated from a suburban area to an urban area with changing ambient air pollution levels and contents in Beijing, China, and provided daily morning/evening peak expiratory flow (PEF) and forced expiratory volume in 1s (FEV₂₁) measurements over 6 months in three study periods. There were significant reductions in evening PEF and morning/evening FEV₂₁ associated with various air pollutants and PM₂.₅ constituents. Four PM₂.₅ constituents (copper, cadmium, arsenic and stannum) were found to be most consistently associated with the reductions in these pulmonary function measures. These findings provide clues for the respiratory effects of specific particulate chemical constituents in the context of urban air pollution. Copyright © 2013 Elsevier B.V. All rights reserved.

  15. [Influence of different methods of chemical disinfection on the physical properties of type IV and V gypsum dies].

    PubMed

    Soares, C R; Ueti, M

    2001-01-01

    Several instruments and materials frequently used in prosthodontics--such as stone casts, dental impressions, interocclusal records--are classified, by the dental literature, as vehicles of transmission of infectious diseases to those who handle them. The present study aims at comparing dimensional alteration, superficial texture and compression resistance of stone dies submitted to different disinfection methods: 30-minute immersion in 1% sodium hypochlorite or in 2.2% alkaline glutaraldehyde (with or without previous ultrasonic washing) and addition of 2.2% alkaline glutaraldehyde or 5% sodium hypochlorite to the gypsum during its preparation. It was possible to conclude that: (1) chemical disinfection did not cause significant dimensional alteration in stone dies; (2) superficial texture was altered according to the disinfection method utilized; (3) immersion in disinfectant solution during 30 min, as well as the addition of disinfectant to the gypsum during its preparation, reduced the compression resistance of dies.

  16. Modeling of the chemical composition of fine particulate matter: Development and performance assessment of EASYWRF-Chem

    NASA Astrophysics Data System (ADS)

    Mendez, M.; Lebègue, P.; Visez, N.; Fèvre-Nollet, V.; Crenn, V.; Riffault, V.; Petitprez, D.

    2016-03-01

    The European emission Adaptation SYstem for the WRF-Chem model (EASYWRF-Chem) has been developed to generate chemical information supporting the WRF-Chem requirements from any emission inventory based on the CORINAIR methodology. Using RADM2 and RACM2 mechanisms, "emission species" are converted into "model species" thanks to the SAPRC methodology for gas phase pollutant and the PM10 and PM2.5 fractions. Furthermore, by adapting US EPA PM2.5 profiles, the processing of aerosol chemical speciation profiles separates the unspeciated PM2.5 emission into five chemical families: sulfates, nitrates, elemental carbon, organic aerosol and unspeciated aerosol. The evaluation of the model has been performed by separately comparing model outcomes with (i) meteorological measurements; (ii) NO2, O3, PM10 and PM2.5 mass concentrations from the regional air quality monitoring network; (iii) hourly-resolved data from four field campaign measurements, in winter and in summer, on two sites in the French northern region. In the latter, a High Resolution - Time of Flight - Aerosol Mass Spectrometer (HR-ToF-AMS) provided non-refractory PM1 concentrations of sulfate, nitrate and ammonium ions as well as organic matter (OM), while an aethalometer provided black carbon (BC) concentrations in the PM2.5 fraction. Meteorological data (temperature, wind, relative humidity) are well simulated for all the time series data except for specific events as wind direction changes or rainfall. For particulate matter, results are presented by considering firstly the total mass concentration of PM2.5 and PM10. EASYWRF-Chem simulations overestimated the PM10 mass concentrations by + 22% and + 4% for summer and winter periods respectively, whereas for the finer PM2.5 fraction, mass concentrations were overestimated by + 20% in summer and underestimated by - 13% in winter. Simulated sulfate concentrations were underestimated and nitrate concentrations were overestimated but hourly variations were well

  17. Near-road sampling of PM2. 5, BC, and fine-particle chemical components in Kathmandu Valley, Nepal

    NASA Astrophysics Data System (ADS)

    Shakya, Kabindra M.; Rupakheti, Maheswar; Shahi, Anima; Maskey, Rejina; Pradhan, Bidya; Panday, Arnico; Puppala, Siva P.; Lawrence, Mark; Peltier, Richard E.

    2017-06-01

    Semicontinuous PM2. 5 and black carbon (BC) concentrations, and 24 h integrated PM2. 5 filter samples were collected near roadways in the Kathmandu Valley, Nepal. Instruments were carried by a group of volunteer traffic police officers in the vicinity of six major roadway intersections in the Kathmandu Valley across two sampling periods in 2014. Daily PM2. 5 filter samples were analyzed for water-soluble inorganic ions, elemental carbon (EC) and organic carbon (OC), and 24 elements. Mean PM2. 5 and BC concentrations were 124.76 µg m-3 and 16.74 µgC m-3 during the drier spring sampling period, and 45.92 µg m-3 and 13.46 µgC m-3 during monsoonal sampling. Despite the lower monsoonal PM2. 5 concentrations, BC and several elements were not significantly lower during the monsoon, which indicates an important contribution of vehicle-related emissions throughout both seasons in this region. During the monsoon, there was an enhanced contribution of chemical species (elements and water-soluble inorganic ions), except secondary inorganic ions, and BC to PM2. 5 (crustal elements: 19 %; heavy metals: 5 %; and BC: 39 %) compared to those in spring (crustal elements: 9 %; heavy metals: 1 %; and BC: 18 %). Silica, calcium, aluminum, and iron were the most abundant elements during both spring and the monsoon, with total concentrations of 12.13 and 8.85 µg m-3, respectively. PM2. 5 and BC showed less spatial variation compared to that for individual chemical species.

  18. First light of the VLT planet finder SPHERE. IV. Physical and chemical properties of the planets around HR8799

    NASA Astrophysics Data System (ADS)

    Bonnefoy, M.; Zurlo, A.; Baudino, J. L.; Lucas, P.; Mesa, D.; Maire, A.-L.; Vigan, A.; Galicher, R.; Homeier, D.; Marocco, F.; Gratton, R.; Chauvin, G.; Allard, F.; Desidera, S.; Kasper, M.; Moutou, C.; Lagrange, A.-M.; Antichi, J.; Baruffolo, A.; Baudrand, J.; Beuzit, J.-L.; Boccaletti, A.; Cantalloube, F.; Carbillet, M.; Charton, J.; Claudi, R. U.; Costille, A.; Dohlen, K.; Dominik, C.; Fantinel, D.; Feautrier, P.; Feldt, M.; Fusco, T.; Gigan, P.; Girard, J. H.; Gluck, L.; Gry, C.; Henning, T.; Janson, M.; Langlois, M.; Madec, F.; Magnard, Y.; Maurel, D.; Mawet, D.; Meyer, M. R.; Milli, J.; Moeller-Nilsson, O.; Mouillet, D.; Pavlov, A.; Perret, D.; Pujet, P.; Quanz, S. P.; Rochat, S.; Rousset, G.; Roux, A.; Salasnich, B.; Salter, G.; Sauvage, J.-F.; Schmid, H. M.; Sevin, A.; Soenke, C.; Stadler, E.; Turatto, M.; Udry, S.; Vakili, F.; Wahhaj, Z.; Wildi, F.

    2016-03-01

    Context. The system of fourplanets discovered around the intermediate-mass star HR8799 offers a unique opportunity to test planet formation theories at large orbital radii and to probe the physics and chemistry at play in the atmospheres of self-luminous young (~30 Myr) planets. We recently obtained new photometry of the four planets and low-resolution (R ~ 30) spectra of HR8799 d and e with the SPHERE instrument (Paper III). Aims: In this paper (Paper IV), we aim to use these spectra and available photometry to determine how they compare to known objects, what the planet physical properties are, and how their atmospheres work. Methods: We compare the available spectra, photometry, and spectral energy distribution (SED) of the planets to field dwarfs and young companions. In addition, we use the extinction from corundum, silicate (enstatite and forsterite), or iron grains likely to form in the atmosphere of the planets to try to better understand empirically the peculiarity of their spectrophotometric properties. To conclude, we use three sets of atmospheric models (BT-SETTL14, Cloud-AE60, Exo-REM) to determine which ingredients are critically needed in the models to represent the SED of the objects, and to constrain their atmospheric parameters (Teff, log g, M/H). Results: We find that HR8799d and e properties are well reproduced by those of L6-L8 dusty dwarfs discovered in the field, among which some are candidate members of young nearby associations. No known object reproduces well the properties of planets b and c. Nevertheless, we find that the spectra and WISE photometry of peculiar and/or young early-T dwarfs reddened by submicron grains made of corundum, iron, enstatite, or forsterite successfully reproduce the SED of these planets. Our analysis confirms that only the Exo-REM models with thick clouds fit (within 2σ) the whole set of spectrophotometric datapoints available for HR8799 d and e for Teff = 1200 K, log g in the range 3.0-4.5, and M/H = +0.5. The

  19. Chemical composition and source of fine and nanoparticles from recent direct injection gasoline passenger cars: Effects of fuel and ambient temperature

    NASA Astrophysics Data System (ADS)

    Fushimi, Akihiro; Kondo, Yoshinori; Kobayashi, Shinji; Fujitani, Yuji; Saitoh, Katsumi; Takami, Akinori; Tanabe, Kiyoshi

    2016-01-01

    Particle number, mass, and chemical compositions (i.e., elemental carbon (EC), organic carbon (OC), elements, ions, and organic species) of fine particles emitted from four of the recent direct injection spark ignition (DISI) gasoline passenger cars and a port fuel injection (PFI) gasoline passenger car were measured under Japanese official transient mode (JC08 mode). Total carbon (TC = EC + OC) dominated the particulate mass (90% on average). EC dominated the TC for both hot and cold start conditions. The EC/TC ratios were 0.72 for PFI and 0.88-1.0 (average = 0.92) for DISI vehicles. A size-resolved chemical analysis of a DISI car revealed that the major organic components were the C20-C28 hydrocarbons for both the accumulation-mode particles and nanoparticles. Contribution of engine oil was estimated to be 10-30% for organics and the sum of the measured elements. The remaining major fraction likely originated from gasoline fuel. Therefore, it is suggested that soot (EC) also mainly originated from the gasoline. In experiments using four fuels at three ambient temperatures, the emission factors of particulate mass were consistently higher with regular gasoline than with premium gasoline. This result suggest that the high content of less-volatile compounds in fuel increase particulate emissions. These results suggest that focusing on reducing fuel-derived EC in the production process of new cars would effectively reduce particulate emission from DISI cars.

  20. Eight-year (2007-2014) trends in ambient fine particulate matter (PM2.5) and its chemical components in the Capital Region of Alberta, Canada.

    PubMed

    Bari, Md Aynul; Kindzierski, Warren B

    2016-05-01

    Currently there have been questions about ambient fine particulate matter (PM2.5) levels in the Capital Region of Alberta, Canada. An investigation of temporal trends in PM2.5 and its chemical components was undertaken in the City of Edmonton within the Capital Region over an 8-year period (2007-2014). A non-parametric trend detection method was adopted to characterize trends in ambient concentrations. No statistically significant change was observed for ambient PM2.5 concentrations during 2007-2014, while significant decreasing trends were found for organic carbon, elemental carbon, oxalate, barium, lead and cadmium. A statistically significant increasing trend was observed for sodium chloride indicating an increase of de-icing salt contribution for winter road maintenance in recent years. Concentrations of potassium ion and zinc exhibited strong and significant seasonal variability with higher concentrations in winter than in summer likely reflecting wood smoke origins more than other potential sources in Edmonton and the surrounding region. No statistically significant changes were observed for all other chemical components examined. Notwithstanding robust population growth that has occurred in Edmonton, these findings reveal that particulate air quality and corresponding trace elements in Edmonton's air has been unchanged or improved over the investigated period (2007-2014). Longer-term air quality monitoring at least over several decades is needed to establish whether trends reported here are actually occurring. Copyright © 2016 Elsevier Ltd. All rights reserved.

  1. Theory of chemical bonds in metalloenzymes IV: Hybrid-DFT study of Rieske-type [2Fe bond 2S] clusters

    NASA Astrophysics Data System (ADS)

    Shoji, Mitsuo; Koizumi, Kenichi; Kitagawa, Yasutaka; Yamanaka, Shusuke; Okumura, Mitsutaka; Yamaguchi, Kizashi

    The Rieske-type [2Fe bond 2S] cores of electron-transfer (ET) proteins in the mitochondrial respiratory chain have unusual properties, such as redox potentials and spectroscopy. In this study, part IV of a series, the inherent molecular structures and characteristic electronic structures of the Rieske-type [2Fe bond 2S] clusters are investigated using broken-symmetry hybrid density functional theory (BS-HDFT). Geometry optimizations for the oxidized and reduced states were performed and their characteristic vibrational modes are assigned. Magnetic properties are investigated using model Hamiltonians to describe the electron delocalization and the unsymmetric property. The parameters of the model Hamiltonian, such as exchange coupling J, valence delocalization B, and potential energy difference ?, are evaluated from the BS-HDFT calculations. The valence localization and excitation energy (?E) of the Rieske-type [2Fe bond 2S] cluster are discussed. The chemical bond nature is characterized by chemical indices from natural orbital analysis. Our theoretical results are reasonably consistent with experimental results.

  2. Comparison between simulated and observed chemical composition of fine aerosols in Paris (France) during springtime: contribution of regional versus continental emissions

    NASA Astrophysics Data System (ADS)

    Sciare, J.; D'Argouges, O.; Sarda-Estève, R.; Gaimoz, C.; Gros, V.; Zhang, Q. J.; Beekmann, M.; Sanchez, O.

    2010-07-01

    Hourly concentrations of inorganic salts (ions) and carbonaceous material in fine aerosols (aerodynamic diameter, A.D.<2.5 μm) have been determined experimentally from fast measurements performed for a 3-week period in spring 2007 in Paris (France). The sum of these two chemical components (ions and carbonaceous aerosols) has shown to account for most of the fine aerosol mass (PM2.5). This time-resolved dataset allowed investigating the factors controlling the levels of PM2.5 in Paris and showed that polluted periods with PM2.5<15 μg/m3 were characterized by air masses of continental (North-Western Europe) origin and chemical composition made by 75% of ions. By contrast, periods with clean marine air masses have shown the lowest PM2.5 concentrations (typically of about 10 μg/m3); carbonaceous aerosols contributing for most of this mass (typically 75%). In order to better discriminate between regional and continental contributions to the observed chemical composition and concentrations of PM2.5 over Paris, a comparative study was performed between this time-resolved dataset and the outputs of a chemistry transport model (CHIMERE), showing a relatively good capability of the model to reproduce the time-limited intense maxima observed in the field for PM2.5 and ion species. Different model scenarios were then investigated switching off regional and European (North-Western and Central) emissions. Results of these scenarios have clearly shown that most of the ions observed over Paris during polluted periods, were either transported or formed in-situ from gas precursors transported from Northern Europe. By opposite, long-range transport from Europe appeared to poorly contribute to the levels of carbonaceous aerosols observed over Paris. The model failed to properly account for the concentration levels and variability of secondary organic aerosols (SOA) determined experimentally by the EC-tracer method. The abundance of SOA (relatively to organic aerosol, OA) was as

  3. Comparison between simulated and observed chemical composition of fine aerosols in Paris (France) during springtime: contribution of regional versus continental emissions

    NASA Astrophysics Data System (ADS)

    Sciare, J.; D'Argouges, O.; Zhang, Q. J.; Sarda-Estève, R.; Gaimoz, C.; Gros, V.; Beekmann, M.; Sanchez, O.

    2010-12-01

    Hourly concentrations of inorganic salts (ions) and carbonaceous material in fine aerosols (aerodynamic diameter, A.D. <2.5 μm) have been determined experimentally from fast measurements performed for a 3-week period in spring 2007 in Paris (France). The sum of these two chemical components (ions and carbonaceous aerosols) has shown to account for most of the fine aerosol mass (PM2.5). This time-resolved dataset allowed investigating the factors controlling the levels of PM2.5 in Paris and showed that polluted periods with PM2.5 > 15 μg m-3 were characterized by air masses of continental (North-Western Europe) origin and chemical composition made by 75% of ions. By contrast, periods with clean marine air masses have shown the lowest PM2.5 concentrations (typically of about 10 μg m-3); carbonaceous aerosols contributing for most of this mass (typically 75%). In order to better discriminate between local and continental contributions to the observed chemical composition and concentrations of PM2.5 over Paris, a comparative study was performed between this time-resolved dataset and the outputs of a chemistry transport model (CHIMERE), showing a relatively good capability of the model to reproduce the time-limited intense maxima observed in the field for PM2.5 and ion species. Different model scenarios were then investigated switching off local and European (North-Western and Central) emissions. Results of these scenarios have clearly shown that most of the ions observed over Paris during polluted periods, were either transported or formed in-situ from gas precursors transported from Northern Europe. On the opposite, long-range transport from Europe appeared to weakly contribute to the levels of carbonaceous aerosols observed over Paris. The model failed to properly account for the concentration levels and variability of secondary organic aerosols (SOA) determined experimentally by the EC-tracer method. The abundance of SOA (relatively to organic aerosol, OA) was as

  4. Fine Particle Sources and Cardiorespiratory Morbidity: An Application of Chemical Mass Balance and Factor Analytical Source-Apportionment Methods

    PubMed Central

    Sarnat, Jeremy A.; Marmur, Amit; Klein, Mitchel; Kim, Eugene; Russell, Armistead G.; Sarnat, Stefanie E.; Mulholland, James A.; Hopke, Philip K.; Tolbert, Paige E.

    2008-01-01

    Background Interest in the health effects of particulate matter (PM) has focused on identifying sources of PM, including biomass burning, power plants, and gasoline and diesel emissions that may be associated with adverse health risks. Few epidemiologic studies, however, have included source-apportionment estimates in their examinations of PM health effects. We analyzed a time-series of chemically speciated PM measurements in Atlanta, Georgia, and conducted an epidemiologic analysis using data from three distinct source-apportionment methods. Objective The key objective of this analysis was to compare epidemiologic findings generated using both factor analysis and mass balance source-apportionment methods. Methods We analyzed data collected between November 1998 and December 2002 using positive-matrix factorization (PMF), modified chemical mass balance (CMB-LGO), and a tracer approach. Emergency department (ED) visits for a combined cardiovascular (CVD) and respiratory disease (RD) group were assessed as end points. We estimated the risk ratio (RR) associated with same day PM concentrations using Poisson generalized linear models. Results There were significant, positive associations between same-day PM2.5 (PM with aero-dynamic diameter ≤ 2.5 μm) concentrations attributed to mobile sources (RR range, 1.018–1.025) and biomass combustion, primarily prescribed forest burning and residential wood combustion, (RR range, 1.024–1.033) source categories and CVD-related ED visits. Associations between the source categories and RD visits were not significant for all models except sulfate-rich secondary PM2.5 (RR range, 1.012–1.020). Generally, the epidemiologic results were robust to the selection of source-apportionment method, with strong agreement between the RR estimates from the PMF and CMB-LGO models, as well as with results from models using single-species tracers as surrogates of the source-apportioned PM2.5 values. Conclusions Despite differences among the

  5. Fast changes in chemical composition and size distribution of fine particles during the near-field transport of industrial plumes.

    PubMed

    Marris, Hélène; Deboudt, Karine; Augustin, Patrick; Flament, Pascal; Blond, François; Fiani, Emmanuel; Fourmentin, Marc; Delbarre, Hervé

    2012-06-15

    Aerosol sampling was performed inside the chimneys and in the close environment of a FeMn alloys manufacturing plant. The number size distributions show a higher abundance of ultrafine aerosols (10-100 nm) inside the plume than upwind of the plant, indicating the emissions of nanoparticles by the industrial process. Individual analysis of particles collected inside the plume shows a high proportion of metal bearing particles (Mn-/Fe-) consisting essentially of internally mixed aluminosilicate and metallic compounds. These particles evolve rapidly (in a few minutes) after emission by adsorption of VOC gas and sulfuric acid emitted by the plant but also by agglomeration with pre-existing particles. At the moment, municipalities require a monitoring of industrial emissions inside the chimneys from manufacturers. However those measures are insufficient to report such rapid changes in chemical composition and thus to evaluate the real impact of industrial plumes in the close environment of plants (when those particles leave the industrial site). Consequently, environmental authorities will have to consider such fast evolutions and then to adapt future regulations on air pollution sources. Copyright © 2012 Elsevier B.V. All rights reserved.

  6. Community-level spatial heterogeneity of chemical constituent levels of fine particulates and implications for epidemiological research

    PubMed Central

    Bell, Michelle L.; Ebisu, Keita; Peng, Roger D.

    2011-01-01

    Studies of the health impacts of airborne particulates’ chemical constituents typically assume spatial homogeneity and estimate exposure from ambient monitors. However, factors such as local sources may cause spatially heterogeneous pollution levels. This work examines the degree to which constituent levels vary within communities and whether exposure misclassification is introduced by spatial homogeneity assumptions. Analysis considered PM2.5 elemental carbon (EC), organic carbon matter, ammonium, sulfate, nitrate, silicon, and sodium ion (Na+) for the United States, 1999–2007. Pearson correlations and coefficients of divergence were calculated and compared to distances among monitors. Linear modeling related correlations to distance between monitors, long-term constituent levels, and population density. Spatial heterogeneity was present for all constituents, yet lower for ammonium, sulfate, and nitrate. Lower correlations were associated with higher distance between monitors, especially for nitrate and sulfate, and with lower long-term levels, especially for sulfate and Na+. Analysis of colocated monitors revealed measurement error for all constituents, especially EC and Na+. Exposure misclassification may be introduced into epidemiological studies of PM2.5 constituents due to spatial variability, and is affected by constituent type and level. When assessing health effects of PM constituents, new methods are needed for estimating exposure and accounting for exposure error induced by spatial variability. PMID:20664652

  7. Massive star formation in Wolf-Rayet galaxies. IV. Colours, chemical-composition analysis and metallicity-luminosity relations

    NASA Astrophysics Data System (ADS)

    López-Sánchez, Á. R.; Esteban, C.

    2010-07-01

    Aims: We have performed a comprehensive multiwavelength analysis of a sample of 20 starburst galaxies that show a substantial population of very young massive stars, most of them classified as Wolf-Rayet (WR) galaxies. In this paper, the forth of the series, we present the global analysis of the derived photometric and chemical properties. Methods: We compare optical/NIR colours and the physical properties (reddening coefficient, equivalent widths of the emission and underlying absorption lines, ionization degree, electron density, and electron temperature) and chemical properties (oxygen abundances and N/O, S/O, Ne/O, Ar/O, and Fe/O ratios) with previous observations and galaxy evolution models. We compile 41 independent star-forming regions - with oxygen abundances between 12 + log(O/H) = 7.58 and 8.75 - , of which 31 have a direct estimate of the electron temperature of the ionized gas. Results: According to their absolute B-magnitude, many of them are not dwarf galaxies, but they should be during their quiescent phase. We found that both c(Hβ) and Wabs increase with increasing metallicity. The differences in the N/O ratio is explained assuming differences in the star formation histories. We detected a high N/O ratio in objects showing strong WR features (HCG 31 AC, UM 420, IRAS 0828+2816, III Zw 107, ESO 566-8 and NGC 5253). The ejecta of the WR stars may be the origin of the N enrichment in these galaxies. We compared the abundances provided by the direct method with those obtained through empirical calibrations, finding that (i) the Pilyugin method is the best suited empirical calibration for these star-forming galaxies; (ii) the relations provided by Pettini & Pagel (2004, MNRAS, 348, 59) give acceptable results for objects with 12 + log(O/H) > 8.0; and (iii) the results provided by empirical calibrations based on photoionization models are systematically 0.2-0.3 dex higher than the values derived from the direct method. The O and N abundances and the N

  8. A one-year comprehensive chemical characterisation of fine aerosol (PM2.5) at urban, suburban and rural background sites in the region of Paris (France)

    NASA Astrophysics Data System (ADS)

    Bressi, M.; Sciare, J.; Ghersi, V.; Bonnaire, N.; Nicolas, J. B.; Petit, J.-E.; Moukhtar, S.; Rosso, A.; Mihalopoulos, N.; Féron, A.

    2013-08-01

    Studies describing the chemical composition of fine aerosol (PM2.5) in urban areas are often conducted for a few weeks only and at one sole site, giving thus a narrow view of their temporal and spatial characteristics. This paper presents a one-year (11 September 2009-10 September 2010) survey of the daily chemical composition of PM2.5 in the region of Paris, which is the second most populated "Larger Urban Zone" in Europe. Five sampling sites representative of suburban (SUB), urban (URB), northeast (NER), northwest (NWR) and south (SOR) rural backgrounds were implemented. The major chemical components of PM2.5 were determined including elemental carbon (EC), organic carbon (OC), and the major ions. OC was converted to organic matter (OM) using the chemical mass closure methodology, which leads to conversion factors of 1.95 for the SUB and URB sites, and 2.05 for the three rural ones. On average, gravimetrically determined PM2.5 annual mass concentrations are 15.2, 14.8, 12.6, 11.7 and 10.8 μg m-3 for SUB, URB, NER, NWR and SOR sites, respectively. The chemical composition of fine aerosol is very homogeneous at the five sites and is composed of OM (38-47%), nitrate (17-22%), non-sea-salt sulfate (13-16%), ammonium (10-12%), EC (4-10%), mineral dust (2-5%) and sea salt (3-4%). This chemical composition is in agreement with those reported in the literature for most European environments. On an annual scale, Paris (URB and SUB sites) exhibits its highest PM2.5 concentrations during late autumn, winter and early spring (higher than 15 μg m-3 on average, from December to April), intermediates during late spring and early autumn (between 10 and 15 μg m-3 during May, June, September, October, and November) and the lowest during summer (below 10 μg m-3 during July and August). PM levels are mostly homogeneous on a regional scale, during the whole project (e.g. for URB plotted against NER sites: slope = 1.06, r2=0.84, n=330), suggesting the importance of mid- or long

  9. A one-year comprehensive chemical characterisation of fine aerosol (PM2.5) at urban, suburban and rural background sites in the region of Paris (France)

    NASA Astrophysics Data System (ADS)

    Bressi, M.; Sciare, J.; Ghersi, V.; Bonnaire, N.; Nicolas, J. B.; Petit, J.-E.; Moukhtar, S.; Rosso, A.; Mihalopoulos, N.; Féron, A.

    2012-11-01

    Studies describing the chemical composition of fine aerosol (PM2.5) in urban areas are often conducted during few weeks only, and at one sole site, giving thus a narrow view of their temporal and spatial characteristics. This paper presents a one-year (11 September 2009-10 September 2010) survey of the daily chemical composition of PM2.5 in the region of Paris, which is the second most populated "Larger Urban Zone" in Europe. Five sampling sites representative of suburban (SUB), urban (URB), northeast (NER), northwest (NWR) and south (SOR) rural backgrounds were implemented. The major chemical components of PM2.5 were determined including elemental carbon (EC), organic carbon (OC), and the major ions. OC was converted to organic matter (OM) using the chemical mass closure methodology, which leads to conversion factors of 1.95 for the SUB and URB sites, and 2.05 for the three rural ones. On average, gravimetrically determined PM2.5 annual mass concentrations are 15.2, 14.8, 12.6, 11.7 and 10.8 μg m-3 for SUB, URB, NER, NWR and SOR sites, respectively. The chemical composition of fine aerosol is very homogeneous at the five sites and is composed of OM (38-47%), nitrate (17-22%), non-sea-salt sulfate (13-16%), ammonium (10-12%), EC (4-10%), mineral dust (2-5%) and sea salt (3-4%). This chemical composition is in agreement with those reported in the literature for most European environments. On the annual scale, Paris (URB and SUB sites) exhibits its highest PM2.5 concentrations during late autumn, winter and early spring (higher than 15 μg m-3 on average, from December to April), intermediates during late spring and early autumn (between 10 and 15 μg m-3 during May, June, September, October, and November) and the lowest during summer (below 10 μg m-3 during July and August). PM levels are mostly homogeneous at the regional scale, on the whole duration of the project (e.g. for URB plotted against NER sites: slope = 1.06, r2 = 0.84, n = 330), suggesting the

  10. Chemical characterization and redox potential of coarse and fine particulate matter (PM) in underground and ground-level rail systems of the Los Angeles Metro.

    PubMed

    Kam, Winnie; Ning, Zhi; Shafer, Martin M; Schauer, James J; Sioutas, Constantinos

    2011-08-15

    A campaign was conducted to assess personal exposure of coarse (2.5 μm < d(p) < 10 μm) and fine (d(p) < 2.5 μm) PM for two lines of the L.A. Metro-a subway (red) and light-rail (gold) line. Concurrent measurements were taken at University of Southern California (USC) to represent ambient conditions. A comprehensive chemical analysis was performed including total and water-soluble metals, inorganic ions, elemental and organic carbon, and organic compounds. Mass balance showed that in coarse PM, iron makes up 27%, 6%, and 2% of gravimetric mass for the red line, the gold line, and USC, respectively; in fine PM, iron makes up 32%, 3%, and 1%. Ambient air is the primary source of inorganic ions and organic compounds for both lines. Noncrustal metals, particularly Cr, Mn, Co, Ni, Mo, Cd, and Eu, were elevated for the red line and, to a lesser degree, the gold line. Mo exhibited the greatest crustal enrichment factors. The enriched species were less water-soluble on the red line than corresponding species on the gold line. Bivariate analysis showed that reactive oxygen species (ROS) activity is strongly correlated with water-soluble Fe (R(2) = 0.77), Ni (R(2 )= 0.95), and OC (R(2 )= 0.92). A multiple linear regression model (R(2) = 0.94, p < 0.001) using water-soluble Fe and OC as predictor variables was developed to explain the variance in ROS. In addition, PM from the red line generates 65% and 55% more ROS activity per m(3) of air than PM from USC and the gold line, respectively; however, one unit of PM mass from the gold line may be as intrinsically toxic as one unit of PM from the red line.

  11. How can [Mo(IV)(CN)6](2-), an apparently octahedral (d)(2) complex, be diamagnetic? Insights from quantum chemical calculations and magnetic susceptibility measurements.

    PubMed

    Radoń, Mariusz; Rejmak, Paweł; Fitta, Magdalena; Bałanda, Maria; Szklarzewicz, Janusz

    2015-06-14

    Quantum chemical calculations are employed to elucidate the origin of a puzzling diamagnetism for a hexacyanomolybdate(IV) anion, [Mo(CN)6](2-), which was previously reported by Szklarzewicz et al. [Inorg. Chem., 2007, 46, 9531-9533]. The diamagnetism is surprising because for the octahedral (d)(2) complex one would rather expect a (paramagnetic) triplet ground state, clearly favored over a (diamagnetic) singlet state by an exchange interaction between two d electrons in the t2g orbitals. Nevertheless, the present calculations reveal that the minimum energy structure of isolated [Mo(CN)6](2-) is not an octahedron, but a trigonal prism; the latter geometry allows maximization of a σ-donation from the cyanides to the electron-deficient Mo(iv) center. Unlike for the octahedron, for the trigonal prism structure the singlet and triplet spin states are close in energy to within a few kcal mol(-1). Although the actual relative energy of the two spin states turns out to be method-dependent, the complete active space calculations (CASPT2; with the appropriate choice of the IPEA shift parameter) can reproduce the singlet ground state, in agreement with the experimentally observed diamagnetism. Moreover, magnetic measurements reveal a slight increase of the magnetic susceptibility with the increase of temperature from 100 to 300 K, suggesting an admixture of a thermally induced paramagnetism (possibly due to Boltzmann population of the low-energy triplet state) on top of the dominant diamagnetism. Our prediction that the geometry of [Mo(CN)6](2-) should significantly deviate from the ideal octahedron, not only in the gas phase, but also in a periodic DFT model of the crystalline phase, as well as the experimentally confirmed diamagnetic properties, does not agree with the previously reported ideal octahedral structure. We suggest that this crystal structure might have been determined incorrectly (e.g., due to overlooked merohedral twinning or superstructure properties) and

  12. Genotoxicity, inflammation and physico-chemical properties of fine particle samples from an incineration energy plant and urban air.

    PubMed

    Sharma, Anoop Kumar; Jensen, Keld Alstrup; Rank, Jette; White, Paul A; Lundstedt, Staffan; Gagne, Remi; Jacobsen, Nicklas R; Kristiansen, Jesper; Vogel, Ulla; Wallin, Håkan

    2007-10-04

    Airborne particulate matter (PM) was sampled by use of an electrostatic sampler in an oven hall and a receiving hall in a waste-incineration energy plant, and from urban air in a heavy-traffic street and from background air in Copenhagen. PM was sampled for 1-2 weeks, four samples at each site. The samples were extracted and examined for mutagenicity in Salmonella typhimurium strains TA98, YG1041 and YG5161, for content of inorganic elements and for the presence of eight polycyclic aromatic hydrocarbons. The induction of IL-6 and IL-8 mRNA expression and the presence of DNA damage - tested by the comet assay - were determined after 24-h incubations with human A549 lung epithelial cells. The PM(2.5) concentration was about twofold greater in the oven hall than in the receiving hall. The particle size distribution in the receiving hall was similar to that in street air (maximum mode at about 25nm), but the distribution was completely different in the oven hall (maximum mode at about 150nm). Also chemically, the samples from the oven hall were highly different from the other samples. PM extracts from the receiving hall, street and background air were more mutagenic than the PM extracts from the oven hall. PM from all four sites caused similar levels of DNA damage in A549 cells; only the oven hall samples gave results that were statistically significantly different from those obtained with street-air samples. The receiving hall and the urban air samples were similarly inflammatory (relative IL-8 mRNA expression), whereas the oven hall did not cause a statistically significant increase in IL-8 mRNA expression. A principal component analysis separated the oven hall and the receiving hall by the first principal component. These two sites were separated from street and background air with the second principal component. Several clusters of constituents were identified. One cluster consisted of all the polycyclic aromatic hydrocarbons (PAH), several groups of metals and one

  13. Chemical partitioning of fine particle-bound metals on haze-fog and non-haze-fog days in Nanjing, China and its contribution to human health risks

    NASA Astrophysics Data System (ADS)

    Li, Huiming; Wu, Hongfei; Wang, Qin'geng; Yang, Meng; Li, Fengying; Sun, Yixuan; Qian, Xin; Wang, Jinhua; Wang, Cheng

    2017-01-01

    Information on chemical partitioning and associated risk of airborne metals, particularly during a haze-fog episode, is limited. Fine particulate matter (PM2.5) was collected during a severe haze-fog event in winter and non-haze-fog periods in summer and fall from an urban region of a typical Chinese mega-city, Nanjing. The particulate-bound metals (Al, As, Ba, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Mo, Na, Ni, Pb, Sr, Ti, V, and Zn) were chemically fractionated in a four-step sequential extraction procedure and human health risk was assessed. During the haze-fog episode, PM2.5 was extremely elevated with a mean concentration of 281 μg/m3 (range: 77-431 μg/m3), whereas the mean PM2.5 concentrations in summer and fall periods were 86 μg/m3 (range: 66-111 μg/m3) and 77 μg/m3 (range: 42-131 μg/m3), respectively. All elements had significantly higher concentrations and many metals exceeded relevant limits on haze-fog days. K, Na, Sr, Zn, Mo, Ca, Cd, Mg, Mn, Cu, Ba, Cr and As all showed relatively high proportions of the soluble and exchangeable fraction and strong bio-accessible potential. High temperature and humidity may increase the bio-accessible fraction of many airborne metals. The hazard index for potential toxic metals was 0.115, which was lower than the safe limit (1). However, the combined carcinogenic risk was 1.32 × 10- 6 for children and 5.29 × 10- 6 for adults, with both values being higher than the precautionary criterion (10- 6). Results of this study provide information for the behavior and risk mitigation of airborne metals.

  14. Chemical Characterization and Source Apportionment of Indoor and Outdoor Fine Particulate Matter (PM2.5) in Retirement Communities of the Los Angeles Basin

    PubMed Central

    Hasheminassab, Sina; Daher, Nancy; Shafer, Martin M.; Schauer, James J.; Delfino, Ralph J.; Sioutas, Constantinos

    2014-01-01

    Concurrent indoor and outdoor measurements of fine particulate matter (PM2.5) were conducted at three retirement homes in the Los Angeles Basin during two separate phases (cold and warm) between 2005 and 2006. Indoor-to-outdoor relationships of PM2.5 chemical constituents were determined and sources of indoor and outdoor PM2.5 were evaluated using a molecular marker-based chemical mass balance (MM-CMB) model. Indoor levels of elemental carbon (EC) along with metals and trace elements were found to be significantly affected by outdoor sources. EC, in particular, displayed very high indoor-to-outdoor (I/O) mass ratios accompanied by strong I/O correlations, illustrating the significant impact of outdoor sources on indoor levels of EC. Similarly, indoor levels of polycyclic aromatic hydrocarbons (PAHs), hopanes, and steranes were strongly correlated with their outdoor components and displayed I/O ratios close to unity. On the other hand, concentrations of n-alkanes and organic acids inside the retirement communities were dominated by indoor sources (e.g. food cooking and consumer products), as indicated by their I/O ratios, which exceeded unity. Source apportionment results revealed that vehicular emissions were the major contributor to both indoor and outdoor PM2.5, accounting for 39 and 46% of total mass, respectively. Moreover, the contribution of vehicular sources to indoor levels was generally comparable to its corresponding outdoor estimate. Other water-insoluble organic matter (other WIOM), which accounts for emissions from uncharacterized primary biogenic sources, displayed a wider range of contributions, varying from 2 to 73% of PM2.5, across all sites and phases of the study. Lastly, higher indoor than outdoor contribution of other water-soluble organic matter (other WSOM) was evident at some of the sites, suggesting the production of secondary aerosols as well as direct emissions from primary sources (including cleaning or other consumer products) at the

  15. Chemical Composition of the Aerosol Fine Fraction during African Dust Events as part of the Dust ATtACk Experiment in the Caribbean Region

    NASA Astrophysics Data System (ADS)

    Vallejo, Pamela; Formenti, Paola; Desboeufs, Karine; Quiñones, Mariana; Chevaillier, Servanne; Santos, Stephanie; Andrews, Elizabeth; Ogren, John A.; Mayol-Bracero, Olga L.

    2015-04-01

    We present results on the assessment of aerosols' chemical composition at the atmospheric observatory of Cabezas de San Juan in Fajardo, Puerto Rico, during the summers of 2011 and 2012, where periods in the presence and absence of dust were studied under the framework of the Dust-ATtACk (Dust- Aging and Transport, from Africa to the Caribbean) experiment. Dust events were identified through observation and using air-mass back-trajectories, Saharan Air Layer images, measurements of aerosol optical thickness (AOT), in situ scattering and absorption coefficients, and chemical analyses. Results obtained for intense dust events were characterized by higher concentration of coarse particles, higher scattering and absorption coefficients (up to 100 Mm-1 and 5 Mm-1 at 550 and 530 nm, respectively), higher AOT (from 0.4 to 0.8) values, and higher concentration of elements associated with mineral dust (e.g., Si μ3 g/m3 compared to background concentrations of 0.15 μg/m3, obtained from XRF analysis). Elemental composition of the fine fraction (Dp < 1.8 μm), analyzed by ICP-OES, also yielded higher average concentrations during dust events of, for example, Fe (0.045 μg m-3, vs 0.016 μg m-3 during low or no dust). Detailed results of the submicron fraction composition for the carbonaceous aerosol (total carbon, organic carbon, black carbon), total nitrogen, the water-soluble organic carbon, water-soluble ions, and the elemental composition with their possible sources will be presented at the meeting.

  16. In Situ Chemical Oxidation of Contaminated Groundwater by Persulfate: Decomposition by Fe(III)- and Mn(IV)-Containing Oxides and Aquifer Materials

    PubMed Central

    2015-01-01

    Persulfate (S2O82–) is being used increasingly for in situ chemical oxidation (ISCO) of organic contaminants in groundwater, despite an incomplete understanding of the mechanism through which it is converted into reactive species. In particular, the decomposition of persulfate by naturally occurring mineral surfaces has not been studied in detail. To gain insight into the reaction rates and mechanism of persulfate decomposition in the subsurface, and to identify possible approaches for improving its efficacy, the decomposition of persulfate was investigated in the presence of pure metal oxides, clays, and representative aquifer solids collected from field sites in the presence and absence of benzene. Under conditions typical of groundwater, Fe(III)- and Mn(IV)-oxides catalytically converted persulfate into sulfate radical (SO4•–) and hydroxyl radical (HO•) over time scales of several weeks at rates that were 2–20 times faster than those observed in metal-free systems. Amorphous ferrihydrite was the most reactive iron mineral with respect to persulfate decomposition, with reaction rates proportional to solid mass and surface area. As a result of radical chain reactions, the rate of persulfate decomposition increased by as much as 100 times when benzene concentrations exceeded 0.1 mM. Due to its relatively slow rate of decomposition in the subsurface, it can be advantageous to inject persulfate into groundwater, allowing it to migrate to zones of low hydraulic conductivity where clays, metal oxides, and contaminants will accelerate its conversion into reactive oxidants. PMID:25133603

  17. In situ chemical oxidation of contaminated groundwater by persulfate: decomposition by Fe(III)- and Mn(IV)-containing oxides and aquifer materials.

    PubMed

    Liu, Haizhou; Bruton, Thomas A; Doyle, Fiona M; Sedlak, David L

    2014-09-02

    Persulfate (S2O8(2-)) is being used increasingly for in situ chemical oxidation (ISCO) of organic contaminants in groundwater, despite an incomplete understanding of the mechanism through which it is converted into reactive species. In particular, the decomposition of persulfate by naturally occurring mineral surfaces has not been studied in detail. To gain insight into the reaction rates and mechanism of persulfate decomposition in the subsurface, and to identify possible approaches for improving its efficacy, the decomposition of persulfate was investigated in the presence of pure metal oxides, clays, and representative aquifer solids collected from field sites in the presence and absence of benzene. Under conditions typical of groundwater, Fe(III)- and Mn(IV)-oxides catalytically converted persulfate into sulfate radical (SO4(•-)) and hydroxyl radical (HO(•)) over time scales of several weeks at rates that were 2-20 times faster than those observed in metal-free systems. Amorphous ferrihydrite was the most reactive iron mineral with respect to persulfate decomposition, with reaction rates proportional to solid mass and surface area. As a result of radical chain reactions, the rate of persulfate decomposition increased by as much as 100 times when benzene concentrations exceeded 0.1 mM. Due to its relatively slow rate of decomposition in the subsurface, it can be advantageous to inject persulfate into groundwater, allowing it to migrate to zones of low hydraulic conductivity where clays, metal oxides, and contaminants will accelerate its conversion into reactive oxidants.

  18. SCRAM: A scoring and ranking system for persistent, bioaccumulative, and toxic substances for the North American Great Lakes. Part IV: Results from representative chemicals, sensitivity analysis, and discriminatory power.

    PubMed

    Snyder, E M; Snyder, S A; Giesy, J P; Blonde, S A; Hurlburt, G K; Summer, C L; Mitchell, R R; Bush, D M

    2000-01-01

    The Chemical Scoring and Ranking Assessment Model (SCRAM) has been described in Parts I-III of this series (Snyder et al.: , 1999a; 1999b; 1999c). SCRAM is a chemical scoring and ranking (CSR) system that scores chemicals on the basis of bioaccumulation potential, environmental persistence, and toxicity. Part IV describes various tests and descriptions of the performance of this system. A group of 21 representative chemicals was chosen and scored to test the system. For those chemicals, the percentages of the scores associated with fate-related properties and associated with data uncertainty were determined. The scoring of four of these chemicals is described in greater detail, and the suitability of the scores is discussed. An analysis of the sensitivity of the system to incomplete data sets is presented. And finally, the discriminatory power of the system is described.

  19. Welding IV.

    ERIC Educational Resources Information Center

    Allegheny County Community Coll., Pittsburgh, PA.

    Instructional objectives and performance requirements are outlined in this course guide for Welding IV, a competency-based course in advanced arc welding offered at the Community College of Allegheny County to provide students with proficiency in: (1) single vee groove welding using code specifications established by the American Welding Society…

  20. Welding IV.

    ERIC Educational Resources Information Center

    Allegheny County Community Coll., Pittsburgh, PA.

    Instructional objectives and performance requirements are outlined in this course guide for Welding IV, a competency-based course in advanced arc welding offered at the Community College of Allegheny County to provide students with proficiency in: (1) single vee groove welding using code specifications established by the American Welding Society…

  1. Fine Arts.

    ERIC Educational Resources Information Center

    Danzer, Gerald A.; Newman, Mark

    1992-01-01

    Discusses the use of fine arts as sources to enrich the study of history. Suggests that such works will serve as barometers of change, examples of cross-cultural influences, and political messages. Includes suggestions of works and artists from different historic periods. (DK)

  2. Fine Arts.

    ERIC Educational Resources Information Center

    Danzer, Gerald A.; Newman, Mark

    1992-01-01

    Discusses the use of fine arts as sources to enrich the study of history. Suggests that such works will serve as barometers of change, examples of cross-cultural influences, and political messages. Includes suggestions of works and artists from different historic periods. (DK)

  3. Study of chemical bonding, physical and biological effect of metformin drug as an organized medicine for diabetes patients with chromium(III) and vanadium(IV) ions.

    PubMed

    Adam, Abdel Majid A; Sharshar, T; Mohamed, Mahmoud A; Ibrahim, Omar B; Refat, Moamen S

    2015-01-01

    New vanadium(IV) and chromium(III) complexes of metformin (MFN) were synthesized upon the chemical interaction between vanadyl(II) sulfate monohydrate or chromium(III) chloride hexahydrate with metformin diabetic drug in the media of a pure grade of methanol solvent. The [(VO)2(MFN)2(SO4)2]2H2O and [Cr(MFN)3]·Cl3·6H2O complexes were discussed using microanalytical measurements, molar conductance, spectroscopic (infrared, ESR, XRD, and UV-vis), effective magnetic moment, scanning electron microscopy (SEM), and thermal analyses (TG/DTG). The elemental analysis shows that VO(II) and Cr(III) complexes were associated with 1:1 and 1:3M ratios, respectively. The infrared spectroscopic results data received from the comparison between free MFN free ligand and their vanadyl(II) and chromium(III) complexes were proven that metformin reacted with respected metal ions as a bidentate ligand through its two imino groups. The kinetic thermodynamic parameters were estimated from the DTG curves. The microstructure changes of the VO(II) and Cr(III) complexes have been probed using positron annihilation lifetime (PAL) and positron annihilation Doppler broadening (PADB) techniques. The PAL and PADB line-shape parameters were found to be dependent on the structure, electronic configuration and molecular weight of metal complexes. Antimicrobial activity of the metformin free ligand and its vanadyl(II) and chromium(III) complexes were evaluated against the gram negative and gram positive bacteria strains and different fungal strains. Moderate antimicrobial activity recorded by disk diffusion inhibition growth zone method in vanadyl(II) and chromium(III) complexes compared to metformin free ligand.

  4. Chemical fractionation of arsenic and heavy metals in fine particle matter and its implications for risk assessment: A case study in Nanjing, China

    NASA Astrophysics Data System (ADS)

    Li, Huiming; Wang, Jinhua; Wang, Qin'geng; Qian, Xin; Qian, Yu; Yang, Meng; Li, Fengying; Lu, Hao; Wang, Cheng

    2015-02-01

    A four-step sequential extraction procedure was used to study the chemical fractionation of As and heavy metals (Cd, Cr, Cu, Fe, Mn, Ni, Pb and Zn) in fine particulate matter (PM2.5) collected from Nanjing, China. The mass concentrations of most PM2.5 samples exceeded the 24 h standard (75 μg/m3) recommended by the new national ambient air quality standard of China. The most abundant elements were Fe, Zn and Pb, while As and Cd were present at the lowest concentrations. As, Cd, Cu, Mn, Pb and Zn were mostly present in the two mobile fractions, including the soluble and exchangeable fraction (F1), and carbonates, oxides and reducible fraction (F2). Fe had the highest proportion present in the residual fraction (F4). Relatively high proportions of the metals Ni and Cr were present in the oxidizable and sulfidic fraction (F3). High proportions of Zn, As and Cu and lower proportions of Cd, Cr and Fe were present in the potentially mobile phases. The enrichment factor, contamination factor and risk assessment code were calculated to analyze the main sources and assess the environmental risks of the metals in PM2.5. The carcinogenic risks of As, Cd, Ni and Pb were all lower than the accepted criterion of 10-6, whereas the carcinogenic risks of Cr for children and As and Cr for adults were higher than 10-6. The non-carcinogenic health risk of As and heavy metals because of PM2.5 exposure for children and adults were lower than but close to the safe level of 1.

  5. Chemical Characterisation of the Coarse and Fine Particulate Matter in the Environment of an Underground Railway System: Cytotoxic Effects and Oxidative Stress—A Preliminary Study

    PubMed Central

    Spagnolo, Anna Maria; Ottria, Gianluca; Perdelli, Fernanda; Cristina, Maria Luisa

    2015-01-01

    Background: Exposure to the particulate matter produced in underground railway systems is arousing increasing scientific interest because of its health effects. The aim of our study was to evaluate the airborne concentrations of PM10 and three sub-fractions of PM2.5 in an underground railway system environment in proximity to platforms and in underground commercial areas within the system, and to compare these with the outdoor airborne concentrations. We also evaluated the metal components, the cytotoxic properties of the various fractions of particulate matter (PM) and their capacity to induce oxidative stress. Method: We collected the coarse fraction (5–10 µm) and the fine fractions (1–2.5 µm; 0.5–1 µm; 0.25–0.5 µm). Chemical characterisation was determined by means of spectrometry. Cytotoxicity and oxidative stress were evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and Reactive Oxygen Species (ROS) assessment. Results: The concentrations of both PM10 and PM2.5 proved to be similar at the three sampling sites. Iron and other transition metals displayed a greater concentration at the subway platform than at the other two sites. The 2.5–10 µm and 1–2.5 µm fractions of PM from all three sampling sites determined a greater increase in ROS; the intensity of oxidative stress progressively declined as particle diameter diminished. Moreover, ROS concentrations were correlated with the concentrations of some transition metals, namely Mn, Cr, Ti, Fe, Cu, Zn, Ni and Mo. All particulate matter fractions displayed lower or similar ROS values between platform level and the outdoor air. Conclusions: The present study revealed that the underground railway environment at platform level, although containing higher concentrations of some particularly reactive metallic species, did not display higher cytotoxicity and oxidative stress levels than the outdoor air. PMID:25872016

  6. Engineering the substrate specificity of cytochrome P450 CYP102A2 by directed evolution: production of an efficient enzyme for bioconversion of fine chemicals.

    PubMed

    Axarli, Irene; Prigipaki, Ariadne; Labrou, Nikolaos E

    2005-06-01

    The P450 cytochromes constitute a large family of hemoproteins that catalyze the monooxygenation of a diversity of hydrophobic substrates. CYP102A2 is a catalytically self-sufficient cytoplasmic enzyme from Bacillus subtilis, containing both a monooxygenase domain and a reductase domain on a single polypeptide chain. CYP102A2 was subjected to error-prone PCR to generate mutants with enhanced activity with fatty acids and other aromatic substrates. The library of CYP102A2 mutants was expressed in BL21(DE3) Escherichia coli cells and screened for their ability to oxidize different substrates by means of an activity assay. After a single round of error-prone PCR, the variant Pro15Ser exhibiting modified substrate specificity was generated. This variant showed approximately 6- to 9-fold increased activity with SDS, lauric acid and 1,4-naphthoquinone, and enhanced activity for other substrates such as ethacrynic acid and epsilon-amino-n-caproic acid. Molecular modeling of the CYP102A2 monooxygenase domain suggested that Pro15 is located in a short helical segment and is involved in extensive interactions between the N-terminal domain and the beta2 sheet, which contribute to the formation of the substrate binding site. Thus, Pro15 appears to affect substrate binding and catalysis indirectly. These results clearly demonstrate the importance of remote residues, not readily predicted by rational design, for the determination of substrate specificity. In addition, we report here that the Pro15Ser variant of CYP102A2 can be efficiently immobilized on epoxy-activated Sepharose at pH 8.5 and 4 degrees C. The immobilized variant of CYP102A2 retains most of its activity (81%) and shows improved stability at 37 degrees C. The approach offers the possibility of designing a P450 bioreactor that can be operated over a long period of time with high efficiency and which can be used in fine chemical synthesis.

  7. Chemical compositions responsible for inflammation and tissue damage in the mouse lung by coarse and fine particulate samples from contrasting air pollution in Europe.

    PubMed

    Happo, Mikko S; Hirvonen, Maija-Riitta; Halinen, Arja I; Jalava, Pasi I; Pennanen, Arto S; Sillanpaa, Markus; Hillamo, Risto; Salonen, Raimo O

    2008-11-01

    Inflammation is regarded as an important mechanism in mortality and morbidity associated with exposures of cardiorespiratory patients to urban air particulate matter. We investigated the association of the chemical composition and sources of urban air fine (PM(2.5-0.2)) and coarse (PM(10-2.5)) particulate samples with the inflammatory activity in the mouse lung. The particulate samples were collected during selected seasons in six European cities using a high-volume cascade impactor. Healthy C57BL/6J mice were intratracheally instilled with a single dose (10 mg/kg) of the particulate samples. At 4, 12, and 24 h after the exposure, the lungs were lavaged and the bronchoalveolar lavage fluid (BALF) was assayed for indicators of inflammation and tissue damage: cell number, total protein, and cytokines (tumor necrosis factor [TNF]-alpha, interleukin [IL]-6, and KC). Dicarboxylic acids and transition metals, especially Ni and V, in PM(2.5-0.2) correlated positively and some secondary inorganic ions (NO3(-), NH4(+)) negatively with the inflammatory activity. Total organic matter and SO4(2-) had no consistent correlations. In addition, the soil-derived constituents (Ca2+, Al, Fe, Si) showed positive correlations with the PM(2.5-0.2)-induced inflammatory activity, but their role in PM(10-2.5) remained obscure, possibly due to largely undefined biogenic material. Markers of poor biomass and coal combustion, i.e., monosaccharide anhydrides and As, were associated with elevated PAH contents in PM(2.5-0.2) and a consistent immunosuppressive effect. Overall, our results support epidemiological findings that the local sources of incomplete combustion and resuspended road dust are important in urban air particulate pollution-related health effects.

  8. Chemical characterisation of the coarse and fine particulate matter in the environment of an underground railway system: cytotoxic effects and oxidative stress-a preliminary study.

    PubMed

    Spagnolo, Anna Maria; Ottria, Gianluca; Perdelli, Fernanda; Cristina, Maria Luisa

    2015-04-13

    Exposure to the particulate matter produced in underground railway systems is arousing increasing scientific interest because of its health effects. The aim of our study was to evaluate the airborne concentrations of PM10 and three sub-fractions of PM2.5 in an underground railway system environment in proximity to platforms and in underground commercial areas within the system, and to compare these with the outdoor airborne concentrations. We also evaluated the metal components, the cytotoxic properties of the various fractions of particulate matter (PM) and their capacity to induce oxidative stress. We collected the coarse fraction (5-10 µm) and the fine fractions (1-2.5 µm; 0.5-1 µm; 0.25-0.5 µm). Chemical characterisation was determined by means of spectrometry. Cytotoxicity and oxidative stress were evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and Reactive Oxygen Species (ROS) assessment. The concentrations of both PM10 and PM2.5 proved to be similar at the three sampling sites. Iron and other transition metals displayed a greater concentration at the subway platform than at the other two sites. The 2.5-10 µm and 1-2.5 µm fractions of PM from all three sampling sites determined a greater increase in ROS; the intensity of oxidative stress progressively declined as particle diameter diminished. Moreover, ROS concentrations were correlated with the concentrations of some transition metals, namely Mn, Cr, Ti, Fe, Cu, Zn, Ni and Mo. All particulate matter fractions displayed lower or similar ROS values between platform level and the outdoor air. The present study revealed that the underground railway environment at platform level, although containing higher concentrations of some particularly reactive metallic species, did not display higher cytotoxicity and oxidative stress levels than the outdoor air.

  9. Physical and chemical properties of feedlot pen surfaces located on moderately coarse- and moderately fine-textured soils in southern Alberta.

    PubMed

    Miller, Jim J; Curtis, Tony; Larney, Francis J; McAllister, Tim A; Olson, Barry M

    2008-01-01

    Southern Alberta has the highest density of feedlot cattle in Canada, and there is a concern that leaching of water and contaminants may be greater for feedlots located on coarser-textured than finer-textured soils. Our objective was to determine if infiltration and leaching were greater for a 4-yr-old feedlot located on a moderately coarse-textured (MC) soil compared with two feedlots located on moderately fine-textured (MF) soils (5- and 52-yr-old pens). Various soil physical properties of feedlot pen surfaces were measured, including field-saturated hydraulic conductivity (K(fs)) and near-saturated hydraulic conductivity at -0.9 and -3.9 cm water potential. Selected chemical properties of feedlot soil layers were measured, as well as the chloride content of the soil profile (0-100 cm). Mean K(fs), K(-0.9), and K(-3.9) values were not significantly (P > 0.10) greater at the MC site than the two MF sites, indicating no evidence of greater infiltration on coarser-textured soils. In addition, mean K(fs), K(-0.9), and K(-3.9) values of soils within feedlot pens at all three sites were significantly (P < or = 0.10) reduced by 46 to 78% compared with soil outside the pens. Depth of chloride accumulation was greatest at the 52-yr-old feedlot on MF soil (60-70 cm), followed by 4-yr-old feedlot on MC soil (40-50 cm) and 5-yr-old feedlot on MF soil (30-40 cm). Visual inspection determined that the black interface layer formed within 2 mo of cattle stocking at all three sites.

  10. Chemical characterization and source apportionment of indoor and outdoor fine particulate matter (PM(2.5)) in retirement communities of the Los Angeles Basin.

    PubMed

    Hasheminassab, Sina; Daher, Nancy; Shafer, Martin M; Schauer, James J; Delfino, Ralph J; Sioutas, Constantinos

    2014-08-15

    Concurrent indoor and outdoor measurements of fine particulate matter (PM2.5) were conducted at three retirement homes in the Los Angeles Basin during two separate phases (cold and warm) between 2005 and 2006. Indoor-to-outdoor relationships of PM2.5 chemical constituents were determined and sources of indoor and outdoor PM2.5 were evaluated using a molecular marker-based chemical mass balance (MM-CMB) model. Indoor levels of elemental carbon (EC) along with metals and trace elements were found to be significantly affected by outdoor sources. EC, in particular, displayed very high indoor-to-outdoor (I/O) mass ratios accompanied by strong I/O correlations, illustrating the significant impact of outdoor sources on indoor levels of EC. Similarly, indoor levels of polycyclic aromatic hydrocarbons (PAHs), hopanes, and steranes were strongly correlated with their outdoor components and displayed I/O ratios close to unity. On the other hand, concentrations of n-alkanes and organic acids inside the retirement communities were dominated by indoor sources (e.g. food cooking and consumer products), as indicated by their I/O ratios, which exceeded unity. Source apportionment results revealed that vehicular emissions were the major contributor to both indoor and outdoor PM2.5, accounting for 39 and 46% of total mass, respectively. Moreover, the contribution of vehicular sources to indoor levels was generally comparable to its corresponding outdoor estimate. Other water-insoluble organic matter (other WIOM), which accounts for emissions from uncharacterized primary biogenic sources, displayed a wider range of contributions, varying from 2 to 73% of PM2.5, across all sites and phases of the study. Lastly, higher indoor than outdoor contribution of other water-soluble organic matter (other WSOM) was evident at some of the sites, suggesting the production of secondary aerosols as well as direct emissions from primary sources (including cleaning or other consumer products) at the

  11. IVS Organization

    NASA Technical Reports Server (NTRS)

    2004-01-01

    International VLBI Service (IVS) is an international collaboration of organizations which operate or support Very Long Baseline Interferometry (VLBI) components. The goals are: To provide a service to support geodetic, geophysical and astrometric research and operational activities. To promote research and development activities in all aspects of the geodetic and astrometric VLBI technique. To interact with the community of users of VLBI products and to integrate VLBI into a global Earth observing system.

  12. Characteristics and Influence of Biosmoke on the Fine-Particle Ionic Composition Measured in Asian Outflow during the Transport and Chemical Evolution Over the Pacific (TRACE-P) Experiment

    NASA Technical Reports Server (NTRS)

    Ma, Y.; Weber, R. J.; Lee, Y.-N.; Orsini, D. A.; Maxwell-Meier, K.; Thornton, D. C.; Bandy, A. R.; Clarke, A. D.; Blake, D. R.; Sachse, G. W.

    2003-01-01

    We investigate the sources, prevalence, and fine-particle inorganic composition of biosmoke over the western Pacific Ocean between 24 February and 10 April 2001. The analysis is based on highly time-resolved airborne measurements of gaseous and fine- particle inorganic chemical composition made during the NASA Transport and Chemical Evolution over the Pacific (TRACE-P) experiment. At latitudes below approximately 25 deg. N, relatively pure biomass burning plumes of enhanced fine-particle potassium, nitrate, ammonium, light-absorbing aerosols, and CO concentrations were observed in plumes that back trajectories and satellite fire map data suggest originated from biomass burning in southeast Asia. Fine-particle water-soluble potassium (K+) is confirmed to be a unique biosmoke tracer, and its prevalence throughout the experiment indicates that approximately 20% of the TRACE-P Asian outflow plumes were influenced, to some extent, by biomass or biofuel burning emissions. At latitudes above 25 deg. N, highly mixed urban/industrial and biosmoke plumes, indicated by SO(sup 2, sub 4) and K+, were observed in 5 out of 53 plumes. Most plumes were found in the Yellow Sea and generally were associated with much higher fine-particle loadings than plumes lacking a biosmoke influence. The air mass back trajectories of these mixed plumes generally pass through the latitude range of between 34 deg. and 40 deg. N on the eastern China coast, a region that includes the large urban centers of Beijing and Tianjin. A lack of biomass burning emissions based on fire maps and high correlations between K+ and pollution tracers (e.g., S(sup 2, sub 4) suggest biofuel sources. Ratios of fine-particle potassium to sulfate are used to provide an estimate of relative contributions of biosmoke emissions to the mixed Asian plumes. The ratio is highly correlated with fine-particle volume (r(sup 2) = 0.85) and predicts that for the most polluted plume encounter in TRACE-P, approximately 60% of the

  13. Characteristics and Influence of Biosmoke on the Fine-Particle Ionic Composition Measured in Asian Outflow during the Transport and Chemical Evolution Over the Pacific (TRACE-P) Experiment

    NASA Technical Reports Server (NTRS)

    Ma, Y.; Weber, R. J.; Lee, Y.-N.; Orsini, D. A.; Maxwell-Meier, K.; Thornton, D. C.; Bandy, A. R.; Clarke, A. D.; Blake, D. R.; Sachse, G. W.

    2003-01-01

    We investigate the sources, prevalence, and fine-particle inorganic composition of biosmoke over the western Pacific Ocean between 24 February and 10 April 2001. The analysis is based on highly time-resolved airborne measurements of gaseous and fine- particle inorganic chemical composition made during the NASA Transport and Chemical Evolution over the Pacific (TRACE-P) experiment. At latitudes below approximately 25 deg. N, relatively pure biomass burning plumes of enhanced fine-particle potassium, nitrate, ammonium, light-absorbing aerosols, and CO concentrations were observed in plumes that back trajectories and satellite fire map data suggest originated from biomass burning in southeast Asia. Fine-particle water-soluble potassium (K+) is confirmed to be a unique biosmoke tracer, and its prevalence throughout the experiment indicates that approximately 20% of the TRACE-P Asian outflow plumes were influenced, to some extent, by biomass or biofuel burning emissions. At latitudes above 25 deg. N, highly mixed urban/industrial and biosmoke plumes, indicated by SO(sup 2, sub 4) and K+, were observed in 5 out of 53 plumes. Most plumes were found in the Yellow Sea and generally were associated with much higher fine-particle loadings than plumes lacking a biosmoke influence. The air mass back trajectories of these mixed plumes generally pass through the latitude range of between 34 deg. and 40 deg. N on the eastern China coast, a region that includes the large urban centers of Beijing and Tianjin. A lack of biomass burning emissions based on fire maps and high correlations between K+ and pollution tracers (e.g., S(sup 2, sub 4) suggest biofuel sources. Ratios of fine-particle potassium to sulfate are used to provide an estimate of relative contributions of biosmoke emissions to the mixed Asian plumes. The ratio is highly correlated with fine-particle volume (r(sup 2) = 0.85) and predicts that for the most polluted plume encounter in TRACE-P, approximately 60% of the

  14. Phthalocyanine as a chemically inert, redox-active ligand: structural and electronic properties of a Nb(IV)-oxo complex incorporating a highly reduced phthalocyanine(4-) anion.

    PubMed

    Wong, Edwin W Y; Walsby, Charles J; Storr, Tim; Leznoff, Daniel B

    2010-04-05

    This report describes the reduction of a niobium(V) phthalocyanine complex and investigation of the electronic structure of the resulting products. The reduction of PcNbCl(3) (Pc = phthalocyanine dianion) with 5.5 equiv of potassium graphite in 1,2-dimethoxyethane (DME) resulted in the isolation of K(2)PcNbO.5DME (1a). Addition of 18-crown-6 to 1a gave [K(18-crown-6)](2)(mu-DME)PcNbO (1b). Both 1a and 1b were structurally characterized by single-crystal X-ray diffraction analysis. In both complexes, the niobium center adopts a square pyramidal geometry and is coordinated by four basal Pc nitrogen atoms and an apical oxo ligand. Notably, the Pc ligand in 1a is saddle-shaped, with significant bond length alternation, rather than flat with delocalized bonding. The production of ethylene during the reduction of PcNbCl(3), detected by gas chromatography/mass spectrometry (GC/MS), suggests that the oxo ligand likely results from double C-O bond activation of DME solvent. A combination of spectroscopic techniques and density functional theory (DFT) calculations were used to establish the electronic structure of 1a. The close correspondence of the electronic absorption spectrum of 1a to that of [PcZn](2-) with a di-reduced Pc(4-) ligand, indicates a similar electronic structure for the two complexes. Evaluation of the electronic transitions for 1a and [PcZn](2-) by time-dependent DFT calculations further suggests a similar electronic structure for both complexes, indicating that differences in symmetry between 1a and [PcZn](2-) do not significantly affect the nature of the electronic transitions. Electron paramagnetic resonance (EPR) spectroscopy of 1a in solution at room temperature gave a 10-line spectrum, while frozen-solution X- and Q-band EPR spectra are consistent with powder-pattern spectra defined by uniaxial g and (93)Nb hyperfine tensors: these imply the presence of a d(1) Nb(IV) metal center. EPR and electron nuclear double resonance spectroscopy suggests that

  15. Chemical characterization and sources of personal exposure to fine particulate matter (PM2.5) in the megacity of Guangzhou, China.

    PubMed

    Chen, Xiao-Cui; Jahn, Heiko J; Engling, Guenter; Ward, Tony J; Kraemer, Alexander; Ho, Kin-Fai; Yim, S H L; Chan, Chuen-Yu

    2017-09-05

    Concurrent ambient and personal measurements of fine particulate matter (PM2.5) were conducted in eight districts of Guangzhou during the winter of 2011. Personal-to-ambient (P-C) relationships of PM2.5 chemical components were determined and sources of personal PM2.5 exposures were evaluated using principal component analysis and a mixed-effects model. Water-soluble inorganic ions (e.g., SO4(2-), NO3(-), NH4(+), C2O4(2-)) and anhydrosugars (e.g., levoglucosan, mannosan) exhibited median personal-to-ambient (P/C) ratios < 1 accompanied by strong P-C correlations, indicating that these constituents in personal PM2.5 were significantly affected by ambient sources. Conversely, elemental carbon (EC) and calcium (Ca(2+)) showed median P/C ratios greater than unity, illustrating significant impact of local traffic, indoor sources, and/or personal activities on individual's exposure. SO4(2-) displayed very low coefficient of divergence (COD) values coupled with strong P-C correlations, implying a uniform distribution of SO4(2-) in the urban area of Guangzhou. EC, Ca(2+), and levoglucosan were otherwise heterogeneously distributed across individuals in different districts. Regional air pollution (50.4 ± 0.9%), traffic-related particles (8.6 ± 0.7%), dust-related particles (5.8 ± 0.7%), and biomass burning emissions (2.0 ± 0.2%) were moderate to high positive sources of personal PM2.5 exposure in Guangzhou. The observed positive and significant contribution of Ca(2+) to personal PM2.5 exposure, highlighting indoor sources and/or personal activities, were driving factors determining personal exposure to dust-related particles. Considerable discrepancies (COD values ranging from 0.42 to 0.50) were shown between ambient concentrations and personal exposures, indicating caution should be taken when using ambient concentrations as proxies for personal exposures in epidemiological studies. Copyright © 2017 Elsevier Ltd. All rights reserved.

  16. The product of microbial uranium reduction includes multiple species with U(IV)-phosphate coordination

    NASA Astrophysics Data System (ADS)

    Alessi, Daniel S.; Lezama-Pacheco, Juan S.; Stubbs, Joanne E.; Janousch, Markus; Bargar, John R.; Persson, Per; Bernier-Latmani, Rizlan

    2014-04-01

    Until recently, the reduction of U(VI) to U(IV) during bioremediation was assumed to produce solely the sparingly soluble mineral uraninite, UO2(s). However, results from several laboratories reveal other species of U(IV) characterized by the absence of an EXAFS U-U pair correlation (referred to here as noncrystalline U(IV)). Because it lacks the crystalline structure of uraninite, this species is likely to be more labile and susceptible to reoxidation. In the case of single species cultures, analyses of U extended X-ray fine structure (EXAFS) spectra have previously suggested U(IV) coordination to carboxyl, phosphoryl or carbonate groups. In spite of this evidence, little is understood about the species that make up noncrystalline U(IV), their structural chemistry and the nature of the U(IV)-ligand interactions. Here, we use infrared spectroscopy (IR), uranium LIII-edge X-ray absorption spectroscopy (XAS), and phosphorus K-edge XAS analyses to constrain the binding environments of phosphate and uranium associated with Shewanella oneidensis MR-1 bacterial cells. Systems tested as a function of pH included: cells under metal-reducing conditions without uranium, cells under reducing conditions that produced primarily uraninite, and cells under reducing conditions that produced primarily biomass-associated noncrystalline U(IV). P X-ray absorption near-edge structure (XANES) results provided clear and direct evidence of U(IV) coordination to phosphate. Infrared (IR) spectroscopy revealed a pronounced perturbation of phosphate functional groups in the presence of uranium. Analysis of these data provides evidence that U(IV) is coordinated to a range of phosphate species, including monomers and polymerized networks. U EXAFS analyses and a chemical extraction measurements support these conclusions. The results of this study provide new insights into the binding mechanisms of biomass-associated U(IV) species which in turn sheds light on the mechanisms of biological U

  17. Thorium nanochemistry: the solution structure of the Th(IV)-hydroxo pentamer.

    PubMed

    Walther, Clemens; Rothe, Jörg; Schimmelpfennig, Bernd; Fuss, Markus

    2012-08-28

    Tetravalent thorium exhibits a strong tendency towards hydrolysis and subsequent polymerization. Polymeric species play a crucial role in understanding thorium solution chemistry, since their presence causes apparent solubility several orders of magnitude higher than predicted by thermodynamic data bases. Although electrospray mass spectrometry (ESI MS) identifies Th(IV) dimers and pentamers unequivocally as dominant species close to the solubility limit, the molecular structure of Th(5)(OH)(y) polymers was hitherto unknown. In the present study, X-ray absorption fine structure (XAFS) spectroscopy, high energy X-ray scattering (HEXS) measurements, and quantum chemical calculations are combined to solve the pentamer structure. The most favourable structure is represented by two Th(IV) dimers linked by a central Th(IV) cation through hydroxide bridges.

  18. Thorium nanochemistry: the solution structure of the Th(IV)-hydroxo pentamer

    SciTech Connect

    Walther, Clemens; Rothe, Jörg; Schimmelpfennig, Bernd; Fuss, Markus

    2012-10-10

    Tetravalent thorium exhibits a strong tendency towards hydrolysis and subsequent polymerization. Polymeric species play a crucial role in understanding thorium solution chemistry, since their presence causes apparent solubility several orders of magnitude higher than predicted by thermodynamic data bases. Although electrospray mass spectrometry (ESI MS) identifies Th(IV) dimers and pentamers unequivocally as dominant species close to the solubility limit, the molecular structure of Th5(OH)y polymers was hitherto unknown. In the present study, X-ray absorption fine structure (XAFS) spectroscopy, high energy X-ray scattering (HEXS) measurements, and quantum chemical calculations are combined to solve the pentamer structure. The most favourable structure is represented by two Th(IV) dimers linked by a central Th(IV) cation through hydroxide bridges.

  19. Observation of fine particle concentration and its chemical characteristics in central region of Korea during KORUS-AQ pre-campaign

    NASA Astrophysics Data System (ADS)

    Lyu, Y.; Lee, M.; Hwang, T.; Hong, Y.; Hong, J.

    2015-12-01

    The Central Region super site is one of the 6 super sites operated in Korean peninsula by Ministry of Environment Korea and monitor air quality of central district of Korea continuously and intensively. Located 160km south of Seoul, this site represents an urban site surrounded by residential, commercial area and an 8-lane road cross section which is one of the most crowed main roads in this area. This site also plays a significant role especially in tracing air pollutants flowing through the West Sea from China. During Korus-AQ(Korea-US Air Quality Study) pre-campaign conducted from 18th May to 12th June, PM2.5 and PM10 mass concentration using BAM1020 (MetOne), PM2.5bounded ion concentration using AIM (URG), metal concentrations using XRF (Cooper), organic and elemental carbon contents using SOCEC (Sunset), light scattering coefficient using Nephelometer (TSI) and meteorological parameters were continuously measured at this super site. PM2.5 and PM10 average concentrations were 31 and 49 ug/m3 with 0.63 fine to course ratio, which were relatively lower than those of annual average concentration of 2014 (39 and 58 ug/m3, respectively). The chemical composition of PM2.5 were determined as ion(46%), TC(37%), CM(2%), TM(0.1%) and unknown(15%). The average concentration of organic and elemental carbon were 5.6 and 1.8 ug/m3 which were similar lever to average of 2014 (5.9 ug/m3, 1.71 ug/m3, respectively). And the metal concentration including Pb(12.5 ng/m3), Fe(151.7 ng/m3), Ca(26.2 ng/m3), Ti(5.2 ng/m3), Cd(4.1 ng/m3) were significantly lower than those of 2014(31.4 ng/m3, 242.1 ng/m3, 167.9 ng/m3, 13.0 ng/m3, 8.3 ng/m3, respectively). However, the average concentration of sulfate was 6.3 ug/m3 which was 43% higher than that of 2014 (4.4 ug/m3). Overall aerosol and its component's concentrations except for secondary sulfate have been decreased since it was late spring and early summer in Korea during pre-campaign and usually in this season aerosol level is

  20. Asteroids IV

    NASA Astrophysics Data System (ADS)

    Michel, Patrick; DeMeo, Francesca E.; Bottke, William F.

    . Asteroids, like planets, are driven by a great variety of both dynamical and physical mechanisms. In fact, images sent back by space missions show a collection of small worlds whose characteristics seem designed to overthrow our preconceived notions. Given their wide range of sizes and surface compositions, it is clear that many formed in very different places and at different times within the solar nebula. These characteristics make them an exciting challenge for researchers who crave complex problems. The return of samples from these bodies may ultimately be needed to provide us with solutions. In the book Asteroids IV, the editors and authors have taken major strides in the long journey toward a much deeper understanding of our fascinating planetary ancestors. This book reviews major advances in 43 chapters that have been written and reviewed by a team of more than 200 international authorities in asteroids. It is aimed to be as comprehensive as possible while also remaining accessible to students and researchers who are interested in learning about these small but nonetheless important worlds. We hope this volume will serve as a leading reference on the topic of asteroids for the decade to come. We are deeply indebted to the many authors and referees for their tremendous efforts in helping us create Asteroids IV. We also thank the members of the Asteroids IV scientific organizing committee for helping us shape the structure and content of the book. The conference associated with the book, "Asteroids Comets Meteors 2014" held June 30-July 4, 2014, in Helsinki, Finland, did an outstanding job of demonstrating how much progress we have made in the field over the last decade. We are extremely grateful to our host Karri Muinonnen and his team. The editors are also grateful to the Asteroids IV production staff, namely Renée Dotson and her colleagues at the Lunar and Planetary Institute, for their efforts, their invaluable assistance, and their enthusiasm; they made life as

  1. Structural Analysis of the Mn(IV)/Fe(III) Cofactor of Chlamydia Trachomatis Ribonucleotide Reductase By Extended X-Ray Absorption Fine Structure Spectroscopy And Density Functional Theory Calculations

    SciTech Connect

    Younker, J.M.; Krest, C.M.; Jiang, W.; Krebs, C.; Bollinger, J.M.Jr.; Green, M.T.

    2009-05-28

    The class Ic ribonucleotide reductase from Chlamydia trachomatis (C{bar A}) uses a stable Mn(lV)/ Fe(lll) cofactor to initiate nucleotide reduction by a free-radical mechanism. Extended X-ray absorption fine structure (EXAFS) spectroscopy and density functional theory (DFT) calculations are used to postulate a structure for this cofactor. Fe and Mn K-edge EXAFS data yield an intermetallic distance of -2.92 {angstrom}. The Mn data also suggest the presence of a short 1.74 {angstrom} Mn-O bond. These metrics are compared to the results of DFT calculations on 12 cofactor models derived from the crystal structure of the inactive Fe2(lll/ III) form of the protein. Models are differentiated by the protonation states of their bridging and terminal OH{sub x} ligands as well as the location of the Mn(lV) ion (site 1 or 2). The models that agree best with experimental observation feature a{mu}-1, 3-carboxylate bridge (E120), terminal solvent (H{sub 2}O/OH) to site 1, one {mu}-O bridge, and one {mu}-OH bridge. The site-placement of the metal ions cannot be discerned from the available data.

  2. Formation of uranium(IV)-silica colloids at near-neutral pH

    NASA Astrophysics Data System (ADS)

    Dreissig, Isabell; Weiss, Stephan; Hennig, Christoph; Bernhard, Gert; Zänker, Harald

    2011-01-01

    Evidence is provided by photon correlation spectroscopy, ultrafiltration and ultracentrifugation that uranium(IV) can form silicate-containing colloids of a size of ⩽20 nm. A concentration of up to 10 -3 M of colloid-borne U(IV) was observed. The particles are generated in near-neutral to slightly alkaline solutions containing background chemicals of geogenic nature (carbonate, silicate, sodium ions). They remain stable in aqueous suspension over years. Electrostatic repulsion due to a negative zeta potential in the near-neutral to alkaline pH range caused by the silicate stabilizes the U(IV) colloids. The isoelectric point of the nanoparticles is shifted toward lower pH values by the silicate. The mechanism of the colloidal stabilization can be regarded as "sequestration" by silicate, a phenomenon well known from heavy metal ions of high ion potential such as iron(III) or manganese(III,IV), but never reported for uranium(IV) so far. Extended X-ray absorption fine structure (EXAFS) spectroscopy showed that U-O-Si bonds, which increasingly replace the U-O-U bonds of the amorphous uranium(IV) oxyhydroxide with increasing silicate concentrations, make up the internal structure of the colloids. The next-neighbor coordination of U(IV) in the U(IV)-silica colloids is comparable with that of coffinite, USiO 4. The assessment of uranium behavior in the aquatic environment should take the possible existence of U(IV)-silica colloids into consideration. Their occurrence might influence uranium migration in anoxic waters.

  3. Band Gap Characters and Ferromagnetic/Antiferromagnetic Coupling in Group-IV Monolayers Tuned by Chemical Species and Hydrogen Adsorption Configurations.

    PubMed

    Yu, Wen-Zhe; Yan, Jia-An; Gao, Shang-Peng

    2015-12-01

    One-side semihydrogenated monolayers of carbon, silicon, germanium, and their binary compounds with different configurations of hydrogen atoms are investigated by density functional theory. Among three considered configurations, zigzag, other than the most studied chair configuration, is energetically the most favorable structure of one-side semihydrogenation. Upon semihydrogenation, the semimetallic silicene, germanene, and SiGe become semiconductors, while the band gap in semiconducting SiC and GeC is reduced. Semihydrogenated silicene, germanene, SiGe, and GeC with chair configuration are found to be ferromagnetic semiconductors. For semihydrogenated SiC, it is ferromagnetic when all hydrogen atoms bond with silicon atoms, while an antiferromagnetic coupling is predicted when all hydrogen atoms bond with carbon atoms. The effect of interatomic distance between two neighboring magnetic atoms to the ferromagnetic or antiferromagnetic coupling is studied. For comparison, properties of one-side and both-side fully hydrogenated group-IV monolayers are also calculated. All fully hydrogenated group-IV monolayers are nonmagnetic semiconductors with band gaps larger than those of their semihydrogenated counterparts.

  4. A method for the concentration of fine-grained rutile (TiO2) from sediment and sedimentary rocks by chemical leaching

    USGS Publications Warehouse

    Commeau, Judith A.; Valentine, Page C.

    1991-01-01

    Most of the sample analyzed by the method described were marine muds collected from the Gulf of Maine (Valentine and Commeau, 1990). The silt and clay fraction (up to 99 wt% of the sediment) is composed of clay minerals (chiefly illite-mica and chlorite), silt-size quartz and feldspar, and small crystals (2-12 um) of rutile and hematite. The bulk sediment samples contained an average of 2 to 3 wt percent CaCO3. Tiher samples analyzed include red and gray Carboniferous and Triassic sandstones and siltstones exposed around the Bay of Fundy region and Paleozoic sandstones, siltstones, and shales from northern Maine and New Brunswick. These rocks are probable sources for the fine-grained rutile found in the Gulf of Maine.

  5. Effect of aluminum on fine structure and distribution of chemical elements in high-entropy alloys Al x FeNiCoCuCr

    NASA Astrophysics Data System (ADS)

    Nadutov, V. M.; Makarenko, S. Yu.; Volosevich, P. Yu.

    2015-05-01

    Electron-microscopic and X-ray diffraction methods have been used to study the fine structure of cast high-entropy alloys (HEAs) Al x FeNiCoCuCr ( x = 1, 1.5, 1.8). Disperse precipitates with dimensions of 130-400 and 10-20 nm have been revealed, the character of distribution of which, as well as the amounts, dimensions, and shapes, change with increasing aluminum content. In the equiatomic HEA, copper-containing particles with an fcc structure have been found; in the alloy with x = 1.8, particles of bcc Al4Cu9 dominate. It has been shown that the most uniform distribution over the matrix is characteristic of Co, unlike other elements, among which Cu and Cr are distributed in the alloy extremely nonuniformly and predominantly enter into the precipitated particles and into clusters in the interparticle spaces, respectively.

  6. Characterization of Caramel Colour IV.

    PubMed

    Licht, B H; Shaw, K; Smith, C; Mendoza, M; Orr, J; Myers, D V

    1992-05-01

    A large number of commercial Caramel Colour IV samples were characterized in order to assess the uniformity of the class and to provide data to be used in specifications development. Owing to the chemical and physical complexity of caramel colour it was not feasible to perform detailed analysis of all constituents for assessment of uniformity. Instead, selected parameters were evaluated and judgements were made with respect to compositional uniformity based on the similarities of these parameters among the various samples. As Caramel Colour IV is required by the food industry in a range of colour intensities, there must be a range of properties that differ from sample to sample, but that are sufficiently similar for the material to still be considered as part of the Caramel Colour IV class. Fractions as well as whole caramel were analysed using selected spectrophotometric, chromatographic and chemical techniques. Samples were fractionated based on molecular weight and polarity. The data presented here provide evidence for the uniformity in composition of Caramel Colour IV with respect to molecular weight distribution, to nitrogen and sulphur content and their distribution throughout the fractions, to absorbance properties and to specific low molecular weight compounds. Thus, it can be concluded that Caramel Colour IV exhibits compositional uniformity within the range of colour intensity required by the food industry worldwide.

  7. Quantitative chemical imaging of element diffusion into heterogeneous media using laser ablation inductively coupled plasma mass spectrometry, synchrotron micro-X-ray fluorescence, and extended X-ray absorption fine structure spectroscopy.

    PubMed

    Wang, H A O; Grolimund, D; Van Loon, L R; Barmettler, K; Borca, C N; Aeschlimann, B; Günther, D

    2011-08-15

    Quantitative chemical imaging of trace elements in heterogeneous media is important for the fundamental understanding of a broad range of chemical and physical processes. The primary aim of this study was to develop an analytical methodology for quantitative high spatial resolution chemical imaging based on the complementary use of independent microanalytical techniques. The selected scientific case study is focused on high spatially resolved quantitative imaging of major elements, minor elements, and a trace element (Cs) in Opalinus clay, which has been proposed as the host rock for high-level radioactive waste repositories. Laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS), providing quantitative chemical information, and synchrotron radiation based micro-X-ray fluorescence (SR-microXRF), providing high spatial resolution images, were applied to study Cs migration into Opalinus clay rock. The results indicate that combining the outputs achievable by the two independent techniques enhances the imaging capabilities significantly. The qualitative high resolution image of SR-microXRF is in good agreement with the quantitative image recorded with lower spatial resolution by LA-ICPMS. Combining both techniques, it was possible to determine that the Opalinus clay sample contains two distinct domains: (i) a clay mineral rich domain and (ii) a calcium carbonate dominated domain. The two domains are separated by sharp boundaries. The spatial Cs distribution is highly correlated to the distribution of the clay. Furthermore, extended X-ray absorption fine structure analysis indicates that the trace element Cs preferentially migrates into clay interlayers rather than into the calcite domain, which complements the results acquired by LA-ICPMS and SR-microXRF. By using complementary techniques, the quantification robustness was improved to quantitative micrometer spatial resolution. Such quantitative, microscale chemical images allow a more detailed

  8. Making Pure Fine-Grained Inorganic Powder

    NASA Technical Reports Server (NTRS)

    Wood, C.

    1985-01-01

    Sustained arc plasma chemical reactor fabricates very-fine-grained inorganic solids having low thermal conductivity. Powder fabrication method, based on plasma tube technique produces pure solids without contamination commonly produced by grinding.

  9. A History of the Chemical Innovations in Silver-Halide Materials for Color Photography(10) IV. Color Print Making by Silver Dye Bleach and Imbibition Processes

    NASA Astrophysics Data System (ADS)

    Oishi, Yasushi

    Prior to the advent of the color photography based on dye-forming development, two color printing processes had been developed: 1) silver dye bleach (commercially introduced as Gasparcolor and then Cibachrome) and 2) imbibtion (introduced as Technicolor). While both processes utilized the available preformed dyes, the former could be said to be a chemical process because it consisted in a single and simple chemical bath of dye destruction, and on the other hand the latter to be a physical process in that the images were formed in multiple mechanical stages of old treatments. Although both processes presented marvelous performances at their earliest phases in the 1930s, they failed to expand their technological frameworks and eventually were surpassed by the dye-forming printing process.

  10. Valuation of characteristics of water purity. IV. Classification of pollution of waters based on norms of microbiological, hydrobiological and chemical characteristics determined by numerical methods.

    PubMed

    Ostrowski, M

    1976-01-01

    Norms of microbiological (coliform titre, nitrification titre, urea hydrolysis titre, number of bacteria, BOD2 and BOD5), hydrobiological (intensity of photosynthesis, saprobic index, number of algae) and chemical (oxidability, DMDT content) characteristics, determining the ecological quality of water, are suggested. Their taxonomic value has been appraised with the use of numerical methods: centrifugal correlation and principle components, used for the classification of a collection of sites with respect to pollution.

  11. Simulation of chemical metabolism for fate and hazard assessment. IV. Computer-based derivation of metabolic simulators from documented metabolism maps.

    PubMed

    Karabunarliev, S; Dimitrov, S; Pavlov, T; Nedelcheva, D; Mekenyan, O

    2012-07-01

    Computer simulation of xenobiotic metabolism and degradation is usually performed proceeding from a set of expert-developed rules modelling the actual enzyme-driven chemical reactions. With the accumulation of extensive metabolic pathway data, the analysis required to derive such chemical reaction patterns has become more objective, but also more convoluted and demanding. Herein we report on our computer-based approach for the analysis of metabolic maps, leading to the construction of reaction rules statistically suitable for simulation purposes. It is based on the set of so-called bare transformations which encompass all unique reaction patterns as obtained by a heuristically enhanced maximum common subgraph algorithm. The bare transformations guarantee that no existing metabolite is missed in simulation at the expense of an enormous amount of false positive predictions. They are rendered more selective by correlating the generated true and false positives to the locations of typical chemical functional groups in the potential reactants. The approach and its results are illustrated for a metabolic map collection of 15 cycloalkanes.

  12. Surface Structure and Chemical Switching of Thioctic Acid Adsorbed on Au(111) as Observed Using Near-Edge X-ray Absorption Fine Structure

    SciTech Connect

    Meulenberg, R W; van Buuren, T; Vance, A L; Terminello, L J; Willey, T M; Bostedt, C; Fadley, C S

    2004-01-06

    Thioctic acid (alpha-lipoic acid) is a molecule with a large disulfide-containing base, a short alkyl-chain with four CH{sub 2} units, and a carboxyl termination. Self-assembled monolayer (SAM) films of thioctic acid adsorbed on Au(111) have been investigated with near-edge x-ray absorption fine structure (NEXAFS) spectroscopy and x-ray photoelectron spectroscopy (XPS) to determine film quality, bonding and morphology. Using standard preparation protocols for SAMs, that is, dissolving thioctic acid in ethanol and exposing gold to the solution, results in poor films. These films are highly disordered, contain a mixture of carboxyl and carboxylate terminations, have more than monolayer coverage, and exhibit unbound disulfide. Conversely, forming films by dissolving 1 mmol thioctic acid into 5% acetic acid in ethanol (as previously reported with carboxyl-terminated alkyl-thiols) forms ordered monolayers with small amounts of unbound sulfur. NEXAFS indicates tilted over endgroups with the carboxyl group normal on average 38{sup o} from the surface normal. Slight dichroism in other features indicates alkyl chains statistically more upright than prostrate on the surface. Reflection-absorption Fourier transform infrared (RA-FTIR) spectra indicate hydrogen bonding between neighboring molecules. In such well-formed monolayers, a stark reorientation occurs upon deprotonation of the endgroup by rinsing in a KOH solution. The carboxylate plane normal is now about 66{sup o} from sample normal, a much more upright orientation. Data indicate this reorientation may also cause a more upright orientation to the alkyl portion of the molecules.

  13. Pt3Ti nanoparticles: fine dispersion on SiO2 supports, enhanced catalytic CO oxidation, and chemical stability at elevated temperatures.

    PubMed

    Saravanan, Govindachetty; Abe, Hideki; Xu, Ya; Sekido, Nobuaki; Hirata, Hirohito; Matsumoto, Shin-ichi; Yoshikawa, Hideki; Yamabe-Mitarai, Yoko

    2010-07-06

    A platinum-based intermetallic phase with an early d-metal, Pt(3)Ti, has been synthesized in the form of nanoparticles (NPs) dispersed on silica (SiO(2)) supports. The organometallic Pt and Ti precursors, Pt(1,5-cyclooctadiene)Cl(2) and TiCl(4)(tetrahydrofuran)(2), were mixed with SiO(2) and reduced by sodium naphthalide in tetrahydrofuran. Stoichiometric Pt(3)Ti NPs with an average particle size of 2.5 nm were formed on SiO(2) (particle size: 20-200 nm) with an atomically disordered FCC-type structure (Fm3m; a = 0.39 nm). A high dispersivity of Pt(3)Ti NPs was achieved by adding excessive amounts of SiO(2) relative to the Pt precursor. A 50-fold excess of SiO(2) resulted in finely dispersed, SiO(2)-supported Pt(3)Ti NPs that contained 0.5 wt % Pt. The SiO(2)-supported Pt(3)Ti NPs showed a lower onset temperature of catalysis by 75 degrees C toward the oxidation reaction of CO than did SiO(2)-supported pure Pt NPs with the same particle size and Pt fraction, 0.5 wt %. The SiO(2)-supported Pt(3)Ti NPs also showed higher CO conversion than SiO(2)-supported pure Pt NPs even containing a 2-fold higher weight fraction of Pt. The SiO(2)-supported Pt(3)Ti NPs retained their stoichiometric composition after catalytic oxidation of CO at elevated temperatures, 325 degrees C. Pt(3)Ti NPs show promise as a catalytic center of purification catalysts for automobile exhaust due to their high catalytic activity toward CO oxidation with a low content of precious metals.

  14. Comparative chemical mass closure of fine and coarse aerosols at two sites in south and west Europe: Implications for EU air pollution policies

    NASA Astrophysics Data System (ADS)

    Viana, M.; Maenhaut, W.; Chi, X.; Querol, X.; Alastuey, A.

    The chemical composition of PM10 and PM2.5 was studied during summer and winter sampling campaigns in South and West Europe (Barcelona, Spain, and Ghent, Belgium). The chemical composition of the PM10 aerosol was markedly different in the two regions, even at similar PM10 levels. The chemical composition of PM2.5 showed more similarities. The contribution of mineral matter was higher in Barcelona (on average 12% of the PM2.5 mass), whereas the contribution from sea salt was higher in Ghent (4% of PM2.5). Volatilisation of NH 4+ from the filters (negative artefact) was observed in both regions, although the extent of this artefact showed regional differences (0-4% and 22-38% of the NH 4+ mass in Ghent and Barcelona, respectively) and had no impact on the compliance with EU limit values. The number of exceedances of the PM10 limit value and an arbitrary PM2.5 limit of 25 μg m -3 was calculated by subtracting the mineral fraction (natural or anthropogenic in origin) from the bulk PM load, and this resulted in the elimination of the PM10 exceedances in Barcelona, and a reduction of one out of three exceedances in Ghent. The subtraction of sea-salt aerosol had no effect in Barcelona, and it removed one exceedance in each size fraction in Ghent. Exceedances of the PM10 daily limit value in Ghent coincided with back-trajectories originating from Eastern and Southern European regions. The origin of the exceedances in Barcelona during the campaigns was mostly local.

  15. Gravimetrical and chemical characterization of SiO x structures deposited on fine powders by short plasma exposure in a plasma down stream reactor

    NASA Astrophysics Data System (ADS)

    Spillmann, Adrian; Sonnenfeld, Axel; Rudolf von Rohr, Philipp

    2008-12-01

    The surface of lactose particles was modified by a plasma-enhanced chemical vapor deposition process to improve the flow behavior of the powder. For this, the particulates were treated in a plasma down stream reactor which provides a short (50 ms) and homogeneous exposure to the capacitively coupled RF discharge. The organosilicon monomer hexamethyldisiloxane (HMDSO) was used as a precursor for the formation of SiO x which is deposited on the substrate particle surface. For varying process gas mixtures (O 2/Ar/HMDSO) and RF power applied, the amount of the deposited material was determined gravimetrically after dissolution of the lactose substrate particles and the chemical composition of the accumulated deposition material was investigated by means of attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy. The concentration of the deposited SiO x relating to the substrate material was found to be in the range of 0.1 wt.%. Based on the ATR-FTIR analysis, the inorganic, i.e. oxidic SiO x fraction of the obtained deposits was shown to be controllable by varying the process parameters, whilst a relatively large amount of organic structures must be considered.

  16. Characterizing phosphorus speciation of Chesapeake Bay sediments using chemical extraction, 31P NMR, and X-ray absorption fine structure spectroscopy.

    PubMed

    Li, Wei; Joshi, Sunendra R; Hou, Guangjin; Burdige, David J; Sparks, Donald L; Jaisi, Deb P

    2015-01-06

    Nutrient contamination has been one of the lingering issues in the Chesapeake Bay because the bay restoration is complicated by temporally and seasonally variable nutrient sources and complex interaction between imported and regenerated nutrients. Differential reactivity of sedimentary phosphorus (P) pools in response to imposed biogeochemical conditions can record past sediment history and therefore a detailed sediment P speciation may provide information on P cycling particularly the stability of a P pool and the formation of one pool at the expense of another. This study examined sediment P speciation from three sites in the Chesapeake Bay: (i) a North site in the upstream bay, (ii) a middle site in the central bay dominated by seasonally hypoxic bottom water, and (iii) a South site at the bay-ocean boundary using a combination of sequential P extraction (SEDEX) and spectroscopic techniques, including (31)P NMR, P X-ray absorption near edge structure spectroscopy (XANES), and Fe extended X-ray absorption fine structure (EXAFS). Results from sequential P extraction reveal that sediment P is composed predominantly of ferric Fe-bound P and authigenic P, which was further confirmed by solid-state (31)P NMR, XANES, and EXAFS analyses. Additionally, solution (31)P NMR results show that the sediments from the middle site contain high amounts of organic P such as monoesters and diesters, compared to the other two sites, but that these compounds rapidly decrease with sediment depth indicating remineralized P could have precipitated as authigenic P. Fe EXAFS enabled to identify the changes in Fe mineral composition and P sinks in response to imposed redox condition in the middle site sediments. The presence of lepidocrocite, vermiculite, and Fe smectite in the middle site sediments indicates that some ferric Fe minerals can still be present along with pyrite and vivianite, and that ferric Fe-bound P pool can be a major P sink in anoxic sediments. These results provide

  17. Fine structure and mineral components of primary calculi in some human prostates.

    PubMed

    Kodaka, Tetsuo; Hirayama, Akihiko; Sano, Tsuneyoshi; Debari, Kazuhiro; Mayahara, Mitsuori; Nakamura, Masanori

    2008-08-01

    The fine structure of prostatic calculi has not been elucidated yet, although the chemical components were reported in detail. We studied the primary or endogenous calculi removed from eight human prostates by secondary scanning electron microscopy, backscattered electron imaging, energy-dispersive X-ray microanalysis and X-ray diffraction. The primary calculi containing Mg, Zn and S, besides Ca and P were basically classified into four stone groups (I-IV) by fine structure and mineral components. Stone I had the core deposits of calcospherites showing concentric rings and the laminated deposits concentrically around the core. Their deposits were identified as apatite. Stone II was occupied with the calcospherite deposits of apatite although the stone growth showed a rough concentric formation. Stone III contained the core of calcospherites and concentric laminated structures, similar to a smaller type of group I, whereas the wider peripheral region was deposited with needle-like structures, identified as calcium oxalates. Stone IV had the core deposits containing small hexahedral structures, identified as whitlockite, which were surrounded with several incompletely concentric laminated bands of apatite. Whitlockite crystals were also found between the fused large calculi. The initial and formative calculi were basically observed as the deposition of mineralizing spherical structures suggesting variously sized corpora amylaceous bodies. Thus, the primary prostatic calculi of stones I-III will begin from the mineralization of amylaceous bodies as a core, while the organic substances, which form stone IV, might be derived from the simple precipitation of prostatic secretion.

  18. The associations between birth weight and exposure to fine particulate matter (PM2.5) and its chemical constituents during pregnancy: A meta-analysis.

    PubMed

    Sun, Xiaoli; Luo, Xiping; Zhao, Chunmei; Zhang, Bo; Tao, Jun; Yang, Zuyao; Ma, Wenjun; Liu, Tao

    2016-04-01

    We performed this meta-analysis to estimate the associations of maternal exposure to PM2.5 and its chemical constituents with birth weight and to explore the sources of heterogeneity in regard to the findings of these associations. A total of 32 studies were identified by searching the MEDLINE, PUBMED, Embase, China Biological Medicine and Wanfang electronic databases before April 2015. We estimated the statistically significant associations of reduced birth weight (β = -15.9 g, 95% CI: -26.8, -5.0) and LBW (OR = 1.090, 95% CI: 1.032, 1.150) with PM2.5 exposure (per 10 μg/m(3) increment) during the entire pregnancy. Trimester-specific analyses showed negative associations between birth weight and PM2.5 exposure during the second (β = -12.6 g) and third (β = -10.0 g) trimesters. Other subgroup analyses indicated significantly different pooled-effect estimates of PM2.5 exposure on birth weight in studies with different exposure assessment methods, study designs and study settings. We further observed large differences in the pooled effect estimates of the PM2.5 chemical constituents for birth weight decrease and LBW. We concluded that PM2.5 exposure during pregnancy was associated with lower birth weight, and late pregnancy might be the critical window. Some specific PM2.5 constituents may have larger toxic effects on fetal weight. Exposure assessment methods, study designs and study settings might be important sources of the heterogeneity among the included studies. Copyright © 2015 The Authors. Published by Elsevier Ltd.. All rights reserved.

  19. Chemical kinetics of Cs species in an alkali-activated municipal solid waste incineration fly ash and pyrophyllite-based system using Cs K-edge in situ X-ray absorption fine structure analysis

    NASA Astrophysics Data System (ADS)

    Shiota, Kenji; Nakamura, Takafumi; Takaoka, Masaki; Nitta, Kiyofumi; Oshita, Kazuyuki; Fujimori, Takashi; Ina, Toshiaki

    2017-05-01

    We conducted in situ X-ray absorption fine structure (in situ XAFS) analysis at the Cs K-edge to investigate the chemical kinetics of Cs species during reaction in an alkali-activated municipal solid waste incineration fly ash (MSWIFA) and pyrophyllite-based system. Understanding the kinetics of Cs is essential to the design of appropriate conditions for Cs stabilization. In situ XAFS analysis of four pastes, prepared from NaOHaq, sodium silicate solution, pyrophyllite, and MSWIFA with the addition of CsCl, was conducted in custom-built reaction cells at four curing temperatures (room temperature, 60 °C, 80 °C, 105 °C) for approximately 34 h. The results indicated that the change in Cs species during reaction at room temperature was small, while changes at higher temperatures were faster and more extreme, with the fastest conversion to pollucite occurring at 105 °C. Further analysis using a leaching test and a simple reaction model for Cs species during reaction showed that the pollucite formation rate was dependent on the curing temperature and had a significant negative correlation with Cs leaching. The activation energy of pollucite formation was estimated to be 31.5 kJ/mol. These results revealed that an important change in the chemical state of Cs occurs during reaction in the system.

  20. Coupled chemical reactions in dynamic nanometric confinement: IV. Ion transmission spectrometric analysis of nanofluidic behavior and membrane formation during track etching in polymers

    NASA Astrophysics Data System (ADS)

    Fink, D.; Vacik, J.; Hnatowicz, V.; Muñoz H, G.; García Arellano, H.; Kiv, A.; Alfonta, L.

    2015-03-01

    In recent papers, it was shown that coupled chemical-topological reactions (CCRs) with both NaOH etchant and silver salts, performed in thin swift-heavy ion-irradiated polymers under the application of a test voltage across the polymer foils, eventually gave rise to characteristic current/voltage features and Bode plots that were tentatively attributed to the formation of Ag2O membranes within the etched tracks. The same was also found when replacing the silver ions by lithium ions, and adding fluoride ions to the NaOH etchant, to promote LiF membrane formation. Ion Transmission Spectrometry (ITS) enabled us to reconfirm the existence of these membranes beyond doubt. The membrane thickness was determined to be ∼0.2-0.4 µm in the best cases. ITS also revealed that hitherto membrane formation occurs only in ∼1% of all tracks, or even less. The reason for this poor abundance seems to be that the decisive factor for membrane formation, which is the firm anchoring of the emerging solid Ag2O or LiF reaction products on the etched track walls, was hitherto rarely fulfilled. We attribute this tentatively to the too high test voltage applied for controlling the CCR process that might hinder the product anchoring on the walls by promoting nanofluidic electromigration. Indeed, voltage reduction seems to improve the situation.

  1. Intelligent Virtual Station (IVS)

    NASA Technical Reports Server (NTRS)

    2002-01-01

    The Intelligent Virtual Station (IVS) is enabling the integration of design, training, and operations capabilities into an intelligent virtual station for the International Space Station (ISS). A viewgraph of the IVS Remote Server is presented.

  2. Intelligent Virtual Station (IVS)

    NASA Technical Reports Server (NTRS)

    2002-01-01

    The Intelligent Virtual Station (IVS) is enabling the integration of design, training, and operations capabilities into an intelligent virtual station for the International Space Station (ISS). A viewgraph of the IVS Remote Server is presented.

  3. Fine Arts Evaluation.

    ERIC Educational Resources Information Center

    Nanaimo School District #68 (British Columbia).

    The fine arts as defined by the Ministry of Education (British Columbia) include music, art, and drama with the curriculum focusing on two concepts: creation and appreciation. One of the aims of School District #68 (Nanaimo) is to provide students with the opportunity to gain exposure to, and experience in, fine arts. The Fine Arts Evaluation…

  4. Ovarian Cancer Stage IV

    MedlinePlus

    ... hyphen, e.g. -historical Searches are case-insensitive Ovarian Cancer Stage IV Add to My Pictures View /Download : ... 1200x1335 View Download Large: 2400x2670 View Download Title: Ovarian Cancer Stage IV Description: Drawing of stage IV shows ...

  5. The FMOS-COSMOS Survey of Star-forming Galaxies at z ≈ 1.6. IV. Excitation State and Chemical Enrichment of the Interstellar Medium

    NASA Astrophysics Data System (ADS)

    Kashino, D.; Silverman, J. D.; Sanders, D.; Kartaltepe, J. S.; Daddi, E.; Renzini, A.; Valentino, F.; Rodighiero, G.; Juneau, S.; Kewley, L. J.; Zahid, H. J.; Arimoto, N.; Nagao, T.; Chu, J.; Sugiyama, N.; Civano, F.; Ilbert, O.; Kajisawa, M.; Le Fèvre, O.; Maier, C.; Masters, D.; Miyaji, T.; Onodera, M.; Puglisi, A.; Taniguchi, Y.

    2017-01-01

    We investigate the physical conditions of ionized gas in high-z star-forming galaxies using diagnostic diagrams based on the rest-frame optical emission lines. The sample consists of 701 galaxies with an Hα detection at 1.4≲ z≲ 1.7, from the Fiber Multi-Object Spectrograph (FMOS)-COSMOS survey, that represent the normal star-forming population over the stellar mass range {10}9.6≲ {M}* /{M}ȯ ≲ {10}11.6, with those at {M}* > {10}11 {M}ȯ being well sampled. We confirm an offset of the average location of star-forming galaxies in the Baldwin–Phillips–Terlevich (BPT) diagram ({{[O}} {{III}}]/{{H}}β versus {{[N}} {{II}}]/{{H}}α ), primarily toward higher {{[O}} {{III}}]/{{H}}β , compared with local galaxies. Based on the [S ii] ratio, we measure an electron density ({n}{{e}}={220}-130+170 {{cm}}-3), which is higher than that of local galaxies. Based on comparisons to theoretical models, we argue that changes in emission-line ratios, including the offset in the BPT diagram, are caused by a higher ionization parameter both at fixed stellar mass and at fixed metallicity, with additional contributions from a higher gas density and possibly a hardening of the ionizing radiation field. Ionization due to active galactic nuclei is ruled out as assessed with Chandra. As a consequence, we revisit the mass–metallicity relation using {{[N}}{{II}}]/{{H}}α and a new calibration including {{[N}} {{II}}]/{{[S}} {{II}}] as recently introduced by Dopita et al. Consistent with our previous results, the most massive galaxies ({M}* ≳ {10}11 {M}ȯ ) are fully enriched, while those at lower masses have metallicities lower than local galaxies. Finally, we demonstrate that the stellar masses, metallicities, and star formation rates of the FMOS sample are well fit with a physically motivated model for the chemical evolution of star-forming galaxies.

  6. Ultraviolet observations of solar fine structure.

    PubMed

    Dere, K P; Bartoe, J D; Brueckner, G E; Cook, J W; Socker, D G

    1987-11-27

    The High Resolution Telescope and Spectrograph was flown on the Spacelab-2 shuttle mission to perform extended observations of the solar chromosphere and transition zone at high spatial and temporal resolution. Ultraviolet spectroheliograms show the temporal development of macrospicules at the solar limb. The C IV transition zone emission is produced in discrete emission elements that must be composed of exceedingly fine (less than 70 kilometers) subresolution structures.

  7. Fluidized-Bed Particles Scavenge Silicon Fines

    NASA Technical Reports Server (NTRS)

    Hsu, G. C.; Rohatgi, N.; Lutwack, R.; Hogle, R.

    1985-01-01

    Waste reduced, and silicon production rate improved. In new process silicon formed by thermal decomposition of SiH4. Part of silicon formed on silicon seed particles as result of surface chemical reaction. However, silicon formed by homogeneous reaction in gas phase tends to form aggregates of silicon atoms, which appear as fine particles (like dust). Believed that scavenging action of seed particles enables large fraction fines to be incorporated onto seed surface. This mode of growth confirmed by electron microscopy photographs.

  8. Association of chemical constituents and pollution sources of ambient fine particulate air pollution and biomarkers of oxidative stress associated with atherosclerosis: A panel study among young adults in Beijing, China.

    PubMed

    Wu, Shaowei; Yang, Di; Wei, Hongying; Wang, Bin; Huang, Jing; Li, Hongyu; Shima, Masayuki; Deng, Furong; Guo, Xinbiao

    2015-09-01

    Ambient particulate air pollution has been associated with increased oxidative stress and atherosclerosis, but the chemical constituents and pollution sources behind the association are unclear. We investigated the associations of various chemical constituents and pollution sources of ambient fine particles (PM2.5) with biomarkers of oxidative stress in a panel of 40 healthy university students. Study participants underwent repeated blood collections for 12 times before and after relocating from a suburban campus to an urban campus with high air pollution levels in Beijing, China. Air pollution data were obtained from central air-monitoring stations, and plasma levels of oxidized low-density lipoprotein (Ox-LDL) and soluble CD36 (sCD36) were determined in the laboratory (n=464). Linear mixed-effects models were used to estimate the changes in biomarkers in association with exposure variables. PM2.5 iron and nickel were positively associated with Ox-LDL (p<0.05). For each interquartile range increase in iron (1-day, 0.51 μg/m(3)) and nickel (2-day, 2.5 ng/m(3)), there were a 1.9% [95% confidence interval (CI): 0.2%, 3.7%] increase and a 1.8% (95% CI: 0.2%, 3.4%) increase in Ox-LDL, respectively. We also found that each interquartile range increase in calcium (1-day, 0.7 μg/m(3)) was associated with a 4.8% (95% CI: 0.7%, 9.1%) increase in sCD36. Among the pollution sources, PM2.5 from traffic emissions and coal combustion were suggestively and positively associated with Ox-LDL. Our findings suggest that a subset of metals in airborne particles may be the major air pollution components that contribute to the increased oxidative stress associated with atherosclerosis.

  9. Incorporation and retention of 99-Tc(IV) in magnetite under high pH conditions.

    PubMed

    Marshall, Timothy A; Morris, Katherine; Law, Gareth T W; Mosselmans, J Frederick W; Bots, Pieter; Parry, Stephen A; Shaw, Samuel

    2014-10-21

    Technetium incorporation into magnetite and its behavior during subsequent oxidation has been investigated at high pH to determine the technetium retention mechanism(s) on formation and oxidative perturbation of magnetite in systems relevant to radioactive waste disposal. Ferrihydrite was exposed to Tc(VII)(aq) containing cement leachates (pH 10.5-13.1), and crystallization of magnetite was induced via addition of Fe(II)aq. A combination of X-ray diffraction (XRD), chemical extraction, and X-ray absorption spectroscopy (XAS) techniques provided direct evidence that Tc(VII) was reduced and incorporated into the magnetite structure. Subsequent air oxidation of the magnetite particles for up to 152 days resulted in only limited remobilization of the incorporated Tc(IV). Analysis of both X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) data indicated that the Tc(IV) was predominantly incorporated into the magnetite octahedral site in all systems studied. On reoxidation in air, the incorporated Tc(IV) was recalcitrant to oxidative dissolution with less than 40% remobilization to solution despite significant oxidation of the magnetite to maghemite/goethite: All solid associated Tc remained as Tc(IV). The results of this study provide the first direct evidence for significant Tc(IV) incorporation into the magnetite structure and confirm that magnetite incorporated Tc(IV) is recalcitrant to oxidative dissolution. Immobilization of Tc(VII) by reduction and incorporation into magnetite at high pH and with significant stability upon reoxidation has clear and important implications for limiting technetium migration under conditions where magnetite is formed including in geological disposal of radioactive wastes.

  10. The role of transferrin in actinide(IV) uptake: comparison with iron(III).

    PubMed

    Jeanson, Aurélie; Ferrand, M; Funke, Harald; Hennig, Christoph; Moisy, Philippe; Solari, Pier Lorenzo; Vidaud, Claude; Den Auwer, Christophe

    2010-01-25

    The impact of actinides on living organisms has been the subject of numerous studies since the 1950s. From a general point of view, these studies show that actinides are chemical poisons as well as radiological hazards. Actinides in plasma are assumed to be mainly complexed to transferrin, the iron carrier protein. This paper casts light on the uptake of actinides(IV) (thorium, neptunium, plutonium) by transferrin, focusing on the pH dependence of the interaction and on a molecular description of the cation binding site in the protein. Their behavior is compared with that of iron(III), the endogenous transferrin cation, from a structural point of view. Complementary spectroscopic techniques (UV/Vis spectrophotometry, microfiltration coupled with gamma spectrometry, and X-ray absorption fine structure) have been combined in order to propose a structural model for the actinide-binding site in transferrin. Comparison of our results with data available on holotransferrin suggests some similarities between the behavior of Fe(III) and Np(IV)/Pu(IV)/ Np(IV) is not complexed at pH <7, whereas at pH approximately 7.4 complexation can be regarded as quantitative. This pH effect is consistent with the in vivo transferrin "cycle". Pu(IV) also appears to be quantitatively bound by apotransferrin at around pH approximately 7.5, whereas Th(IV) was never complexed under our experimental conditions. EXAFS data at the actinide edge have allowed a structural model of the actinide binding site to be elaborated: at least one tyrosine residue could participate in the actinide coordination sphere (two for iron), forming a mixed hydroxo-transferrin complex in which actinides are bound with transferrin both through An-tyrosine and through An--OH bonds. A description of interatomic distances is provided.

  11. Energy levels and lifetimes of Nd IV, Pm IV, Sm IV, and Eu IV

    SciTech Connect

    Dzuba, V. A.; Safronova, U. I.; Johnson, W. R.

    2003-09-01

    To address the shortage of experimental data for electron spectra of triply ionized rare-earth elements we have calculated energy levels and lifetimes of 4f{sup n+1} and 4f{sup n}5d configurations of Nd IV (n=2), Pm IV (n=3), Sm IV (n=4), and Eu IV (n=5) using Hartree-Fock and configuration-interaction methods. To control the accuracy of our calculations we also performed similar calculations for Pr III, Nd III, and Sm III, for which experimental data are available. The results are important, in particular, for physics of magnetic garnets.

  12. Production of fine chemicals using biocatalysis.

    PubMed

    Liese, A; Filho, M V

    1999-12-01

    Presently, a large number of biotransformations are carried out on an industrial scale and are discussed in a fast increasing number of reviews. Besides this, a significant number of biotransformations have been investigated over the past year, from degrading to transforming and synthetic reactions. The development of more specific and stable biocatalysts, either isolated enzymes or whole cells, generated by the new methods of genetic engineering and improved by reaction engineering have led to new industrial biotransformations.

  13. Mississippi Fine Arts Framework.

    ERIC Educational Resources Information Center

    Mississippi State Dept. of Education, Jackson.

    The Mississippi Fine Arts Framework is designed to develop K-12 students' interest and expertise in dance, music, theater arts, and visual arts. The introductory fine arts course, for secondary level students, explores the relationship and the function of the arts in both historical and contemporary culture through creative projects, performance,…

  14. Using PLATO IV.

    ERIC Educational Resources Information Center

    Meller, David V.

    This beginning reference manual describes PLATO IV hardware for prospective users and provides an introduction to PLATO for new authors. The PLATO terminal is described in detail in Chapter 1. Chapter 2 provides a block diagram of the PLATO IV system. Procedures for getting on line are described in Chapter 3, and Chapter 4 provides references to…

  15. Flow-injection chemiluminescence determination of enrofloxacin using the Ru(phen)3(2+)-Ce(IV) system and central composite design for the optimization of chemical variables.

    PubMed

    Rezaei, B; Mokhtari, A

    2008-01-01

    The main purpose of this study was to develop an inexpensive, simple, rapid and sensitive chemiluminescence (CL) method for the determination of enrofloxacin (ENRO) using a flow-injection system. This method is based on rapid reduction of Ru(phen)(3)(3+), which is produced in the reaction between Ru(phen)(3)(2+) and acidic Ce(IV) by ENRO, producing strong CL. A central composite design (CCD) was used for optimization of the chemical variables. Regression analysis of the data from the CCD demonstrated that a second-order polynomial model is an adequate description of the surface over the factor limits studied. Optimization using CCD gave approximately four-fold better results than the single-factor-at-a-time method. Under optimal experimental conditions, the CL response was proportional to the concentration of ENRO over a wide range (0.008-3.6 microg/mL) with a correlation coefficient of 0.9986 and a detection limit of 0.003 microg/mL (3sigma). The relative standard deviation for 11 repeated determinations of 0.14 microg/mL ENRO was 4.2%. This method was successfully applied to the analysis of commercial formulations, spiked plasma and spiked poultry tissue. Sample analyses showed good recovery percentages for drugs and spiked plasma (95.1-103.9%). Recovery percentages for spiked poultry tissue were in the range 77.6-87.3%. The minimum sampling rate was 100 samples/h. (c) 2008 John Wiley & Sons, Ltd.

  16. Inhibitory Effect of Dissolved Silica on the H2O2 Decomposition by Iron(III) and Manganese(IV) Oxides: Implications for H2O2-based In Situ Chemical Oxidation

    PubMed Central

    Pham, Anh Le-Tuan; Doyle, Fiona M.; Sedlak, David L.

    2011-01-01

    The decomposition of H2O2 on iron minerals can generate •OH, a strong oxidant that can transform a wide range of contaminants. This reaction is critical to In Situ Chemical Oxidation (ISCO) processes used for soil and groundwater remediation, as well as advanced oxidation processes employed in waste treatment systems. The presence of dissolved silica at concentrations comparable to those encountered in natural waters decreases the reactivity of iron minerals toward H2O2, because silica adsorbs onto the surface of iron minerals and alters catalytic sites. At circumneutral pH values, goethite, amorphous iron oxide, hematite, iron-coated sand and montmorillonite that were pre-equilibrated with 0.05 – 1.5 mM SiO2 were significantly less reactive toward H2O2 decomposition than their original counterparts, with the H2O2 loss rates inversely proportional to the SiO2 concentration. In the goethite/H2O2 system, the overall •OH yield, defined as the percentage of decomposed H2O2 producing •OH, was almost halved in the presence of 1.5 mM SiO2. Dissolved SiO2 also slows the H2O2 decomposition on manganese(IV) oxide. The presence of dissolved SiO2 results in greater persistence of H2O2 in groundwater, lower H2O2 utilization efficiency and should be considered in the design of H2O2-based treatment systems. PMID:22129132

  17. Inhibitory effect of dissolved silica on H₂O₂ decomposition by iron(III) and manganese(IV) oxides: implications for H₂O₂-based in situ chemical oxidation.

    PubMed

    Pham, Anh Le-Tuan; Doyle, Fiona M; Sedlak, David L

    2012-01-17

    The decomposition of H(2)O(2) on iron minerals can generate •OH, a strong oxidant that can transform a wide range of contaminants. This reaction is critical to In Situ Chemical Oxidation (ISCO) processes used for soil and groundwater remediation, as well as advanced oxidation processes employed in waste treatment systems. The presence of dissolved silica at concentrations comparable to those encountered in natural waters decreases the reactivity of iron minerals toward H(2)O(2), because silica adsorbs onto the surface of iron minerals and alters catalytic sites. At circumneutral pH values, goethite, amorphous iron oxide, hematite, iron-coated sand, and montmorillonite that were pre-equilibrated with 0.05-1.5 mM SiO(2) were significantly less reactive toward H(2)O(2) decomposition than their original counterparts, with the H(2)O(2) loss rates inversely proportional to SiO(2) concentrations. In the goethite/H(2)O(2) system, the overall •OH yield, defined as the percentage of decomposed H(2)O(2) producing •OH, was almost halved in the presence of 1.5 mM SiO(2). Dissolved SiO(2) also slowed H(2)O(2) decomposition on manganese(IV) oxide. The presence of dissolved SiO(2) results in greater persistence of H(2)O(2) in groundwater and lower H(2)O(2) utilization efficiency and should be considered in the design of H(2)O(2)-based treatment systems.

  18. The determination of uranium (IV) in apatite

    USGS Publications Warehouse

    Clarke, Roy S.; Altschuler, Zalman S.

    1956-01-01

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

  19. A "Fine" Relationship: OSHA and Schools.

    ERIC Educational Resources Information Center

    O'Neill, Steve

    2001-01-01

    To avoid California schools' experience with Occupational Safety and Health Administration fines, principals should comply with safety regulations, establish quick-response procedures, take care of chemicals, prepare site personnel for state OSHA visits, inform safety personnel about procedures for appealing citations, keep good records, and work…

  20. IV treatment at home

    MedlinePlus

    ... venous catheter - home; Port - home; PICC line - home; Infusion therapy - home; Home health care - IV treatment ... is given quickly, all at once. A slow infusion, which means the medicine is given slowly over ...

  1. Fine motor control

    MedlinePlus

    ... with Parkinson disease have trouble speaking, eating, and writing because they have lost fine motor control. The ... Drawing lines or circles Folding clothes Holding and writing with a pencil Stacking blocks Zipping a zipper

  2. Selenium extractability from a contaminated fine soil fraction: implication on soil cleanup.

    PubMed

    Lim, Teik-Thye; Goh, Kok-Hui

    2005-01-01

    Two batches of fine soil fraction of an acidic soil were deliberately contaminated with selenite (Se(IV)) and selenate (Se(VI)), respectively, and aged for more than 220 days. Speciation analysis using continuous flow-through hydride generation atomic absorption spectrometry (HGAAS) indicated that the species were predominant in their respective aged soils. A selective sequential extraction scheme was employed to fractionate the Se retained in the soils into six fractions of varying retentions. Abilities of various chemical reagents in extracting the Se in the two soil batches were then evaluated. The reagents investigated were sodium salts such as sodium chloride (NaCl), sodium sulfate (Na2SO4), sodium carbonate (Na2CO3), and sodium phosphate (Na3PO4), and two oxidants, namely, hydrogen peroxide (H2O2) and potassium permanganate (KMnO4). It was found that NaCl, Na2SO4, and Na2CO3 could only extract the exchangeable fraction of Se, while Na3PO4 could extract the exchangeable and strongly-bound fractions. Selenate was extracted more than Se(IV) by the salts. The kinetics of Se(IV) extraction by Na3PO4 could be best described by the Elovich model, while the Ritchie second-order model was the most appropriate to describe Se(VI) extraction. Efficiencies of the oxidants in Se(IV) extraction highly depended on their applied dosages. Both H2O2 and KMnO4 were able to extract greater than 93% of total Se, and therefore were significantly more effective than the salts in Se(IV) extraction.

  3. GCF Mark IV development

    NASA Technical Reports Server (NTRS)

    Mortensen, L. O.

    1982-01-01

    The Mark IV ground communication facility (GCF) as it is implemented to support the network consolidation program is reviewed. Changes in the GCF are made in the area of increased capacity. Common carrier circuits are the medium for data transfer. The message multiplexing in the Mark IV era differs from the Mark III era, in that all multiplexing is done in a GCF computer under GCF software control, which is similar to the multiplexing currently done in the high speed data subsystem.

  4. Search for alpha variation in UVES spectra: Analysis of C IV and Si IV doublets towards QSO 1101-264

    NASA Astrophysics Data System (ADS)

    Martínez Fiorenzano, A. F.; Vladilo, G.; Bonifacio, P.

    Motivated by previous studies of QSO spectra that reported a variation of the fine structure constant alpha , a search for C IV and Si IV doublets was conducted in the absorption spectrum toward QSO 1101-264, obtained by VLT-UVES during the Science Verification. Seven C IV and two Si IV systems were identified and accurate measurements of wavelengths over the redshift range 1.1862 < z < 1.8377 were performed. After a careful selection of pairs of lines, the ``Alkali Doublet" method with a derived analitical expression for the error analysis was applied to compute the alpha variation. The result according in magnitud order with previous doublets measurements, corresponds to one Si IV system: Delta alpha /alpha = (- 3.09 +/- 8.46) x 10-5. Data from UVES-VLT.

  5. Modeling sulfur dioxide absorption by fine water spray

    SciTech Connect

    Cheng-Hsiung Huang

    2005-07-01

    A novel theoretical model was developed to determine the removal efficiency of sulfur dioxide using fine water spray. The droplet pH, diameter, S(IV) concentration, sulfur dioxide concentration, and liquid-to-gas ratio are found to influence the absorption of sulfur dioxide by the fine water spray. The results demonstrate that the absorption of sulfur dioxide by the fine water spray increases as the droplet diameter falls. The concentration gradient between the interface of the gaseous and liquid phases causes the absorption of sulfur dioxide by the droplets to increase as the initial S(IV) concentration decreases or the sulfur dioxide concentration increases. The results indicate that the performance of the fine water spray in removing sulfur dioxide is generally improved by reducing the droplet diameter or the initial S(IV) concentration, or by increasing the sulfur dioxide concentration, the droplet pH or the liquid-to-gas ratio. The proposed model reveals the parameters that should be controlled in using a fine water spray device and a method for improving its performance in removing sulfur dioxide.

  6. Aqueous chemistry of Ce(iv): estimations using actinide analogues.

    PubMed

    Marsac, Rémi; Réal, Florent; Banik, Nidhu Lal; Pédrot, Mathieu; Pourret, Olivier; Vallet, Valérie

    2017-10-10

    The prediction of cerium (Ce) aqueous speciation is relevant in many research fields. Indeed, Ce compounds are used for many industrial applications, which may require the control of Ce aqueous chemistry for their synthesis. The aquatic geochemistry of Ce is also of interest. Due to its growing industrial use and its release into the environment, Ce is now considered as an emerging contaminant. Cerium is also used as a proxy of (paleo)redox conditions due to the Ce(iv)/Ce(iii) redox transition. Finally, Ce(iv) is often presented as a relevant analogue of tetravalent actinides (An(iv)). In the present study, quantum chemical calculations were conducted to highlight the similarities between the structures of Ce(iv) and tetravalent actinide (An(iv); An = Th, Pa, U, Np, Pu) aqua-ions, especially Pu(iv). The current knowledge of An(iv) hydrolysis, solubility and colloid formation in water was briefly reviewed but important discrepancies were observed in the available data for Ce(iv). Therefore, new estimations of the hydrolysis constants of Ce(iv) and the solubility of Ce(iv)-(hydr)oxides are proposed, by analogy with Pu(iv). By plotting pH-Eh (Pourbaix) diagrams, we showed that the pH values corresponding to the onset of Ce(iv) species formation (i.e. Ce(iv)-(hydr)oxide or dissolved Ce(iv)) agreed with various experimental results. Although further experimental studies are required to obtain a more accurate thermodynamic database, the present work might yet help to predict more accurately the Ce chemical behavior in aqueous solution.

  7. Interplanetary Type IV Bursts

    NASA Astrophysics Data System (ADS)

    Hillaris, A.; Bouratzis, C.; Nindos, A.

    2016-08-01

    We study the characteristics of moving type IV radio bursts that extend to hectometric wavelengths (interplanetary type IV or type {IV}_{{IP}} bursts) and their relationship with energetic phenomena on the Sun. Our dataset comprises 48 interplanetary type IV bursts observed with the Radio and Plasma Wave Investigation (WAVES) instrument onboard Wind in the 13.825 MHz - 20 kHz frequency range. The dynamic spectra of the Radio Solar Telescope Network (RSTN), the Nançay Decametric Array (DAM), the Appareil de Routine pour le Traitement et l' Enregistrement Magnetique de l' Information Spectral (ARTEMIS-IV), the Culgoora, Hiraso, and the Institute of Terrestrial Magnetism, Ionosphere and Radio Wave Propagation (IZMIRAN) Radio Spectrographs were used to track the evolution of the events in the low corona. These were supplemented with soft X-ray (SXR) flux-measurements from the Geostationary Operational Environmental Satellite (GOES) and coronal mass ejections (CME) data from the Large Angle and Spectroscopic Coronagraph (LASCO) onboard the Solar and Heliospheric Observatory (SOHO). Positional information of the coronal bursts was obtained by the Nançay Radioheliograph (NRH). We examined the relationship of the type IV events with coronal radio bursts, CMEs, and SXR flares. The majority of the events (45) were characterized as compact, their duration was on average 106 minutes. This type of events was, mostly, associated with M- and X-class flares (40 out of 45) and fast CMEs, 32 of these events had CMEs faster than 1000 km s^{-1}. Furthermore, in 43 compact events the CME was possibly subjected to reduced aerodynamic drag as it was propagating in the wake of a previous CME. A minority (three) of long-lived type {IV}_{{IP}} bursts was detected, with durations from 960 minutes to 115 hours. These events are referred to as extended or long duration and appear to replenish their energetic electron content, possibly from electrons escaping from the corresponding coronal

  8. New methods and standards for fine dust

    NASA Astrophysics Data System (ADS)

    Spielvogel, Jürgen; Hartstock, Stefan; Grimm, Hans

    2009-05-01

    There seems to be common agreement that PM10 is a suboptimal quantity for the quantification of potential dangers from fine dust due to a number of reasons, notably because the chemical composition of the particles is not considered, because the size distribution is disregarded, and because of sampling artefacts. In a first step for improving the particle measurements, the European Community has published new directives for ambient air in June 2008 (EU 2008), which as a main part included new regulations for PM2.5 measurements, in addition to the further on valid regulations for PM10. The comparison of PM2.5 and PM10 may allow a source apportionment and a better assessment of the influence of fine dust on human health. The source apportionment may allow more effective fine dust reduction strategies.

  9. The PLATO IV Architecture.

    ERIC Educational Resources Information Center

    Stifle, Jack

    The PLATO IV computer-based instructional system consists of a large scale centrally located CDC 6400 computer and a large number of remote student terminals. This is a brief and general description of the proposed input/output hardware necessary to interface the student terminals with the computer's central processing unit (CPU) using available…

  10. PLATO IV Accountancy Index.

    ERIC Educational Resources Information Center

    Pondy, Dorothy, Comp.

    The catalog was compiled to assist instructors in planning community college and university curricula using the 48 computer-assisted accountancy lessons available on PLATO IV (Programmed Logic for Automatic Teaching Operation) for first semester accounting courses. It contains information on lesson access, lists of acceptable abbreviations for…

  11. Little Jiffy, Mark IV

    ERIC Educational Resources Information Center

    Kaiser, Henry F.; Rice, John

    1974-01-01

    In this paper three changes and one new development for the method of exploratory factor analysis (a second generation Little Jiffy) developed by Kaiser are described. Following this short description a step-by-step computer algorithm of the revised method, dubbed Little Jiffy, Mark IV is presented. (MP)

  12. IVS Technology Coordinator Report

    NASA Technical Reports Server (NTRS)

    Whitney, Alan

    2013-01-01

    This report of the Technology Coordinator includes the following: 1) continued work to implement the new VLBI2010 system, 2) the 1st International VLBI Technology Workshop, 3) a VLBI Digital- Backend Intercomparison Workshop, 4) DiFX software correlator development for geodetic VLBI, 5) a review of progress towards global VLBI standards, and 6) a welcome to new IVS Technology Coordinator Bill Petrachenko.

  13. Internal Fine Structure of Ellerman Bombs

    NASA Astrophysics Data System (ADS)

    Hashimoto, Yuki; Kitai, Reizaburo; Ichimoto, Kiyoshi; Ueno, Satoru; Nagata, Shin'ichi; Ishii, Takako T.; Hagino, Masaoki; Komori, Hiroyuki; Nishida, Keisuke; Matsumoto, Takuma; Otsuji, Kenichi; Nakamura, Tahei; Kawate, Tomoko; Watanabe, Hiroko; Shibata, Kazunari

    2010-08-01

    We conducted coordinated observations of Ellerman bombs (EBs) between Hinode Satellite and Hida Observatory (HOP12). CaII H broad-band filter images of NOAA 10966 on 2007 August 9 and 10 were obtained with the Solar Optical Telescope (SOT) aboard the Hinode Satellite, and many bright points were observed. We identified a total of 4 bright points as EBs, and studied the temporal variation of their morphological fine structures and spectroscopic characteristics. With high-resolution CaII H images of SOT, we found that the EBs, thus far thought of as single bright features, are composed of a few of fine subcomponents. Also, by using Stokes I/V filtergrams with Hinode/SOT, and CaII H spectroheliograms with Hida/Domeless Solar Telescope (DST), our observation showed: (1) The mean duration, the mean width, the mean length, and the mean aspect ratio of the subcomponents were 390 s, 170 km, 450 km, and 2.7, respectively. (2) Subcomponents started to appear on the magnetic neutral lines, and extended their lengths from the original locations. (3) When the CaII H line of EBs showed the characteristic blue asymmetry, they are associated with the appearance or re-brightening of subcomponents. Summarizing our results, we obtained an observational view that elementary magnetic reconnections take place one by one successively and intermittently in EBs, and that their manifestation is the fine subcomponents of the EB phenomena.

  14. Enhanced Design Alternative IV

    SciTech Connect

    N. E. Kramer

    1999-05-18

    This report evaluates Enhanced Design Alternative (EDA) IV as part of the second phase of the License Application Design Selection (LADS) effort. The EDA IV concept was compared to the VA reference design using criteria from the ''Design Input Request for LADS Phase II EDA Evaluations'' (CRWMS M&O 1999b) and (CRWMS M&O 1999f). Briefly, the EDA IV concept arranges the waste packages close together in an emplacement configuration known as ''line load''. Continuous pre-closure ventilation keeps the waste packages from exceeding the 350 C cladding and 200 C (4.3.13) drift wall temperature limits. This EDA concept keeps relatively high, uniform emplacement drift temperatures (post-closure) to drive water away from the repository and thus dry out the pillars between emplacement drifts. The waste package is shielded to permit human access to emplacement drifts and includes an integral filler inside the package to reduce the amount of water that can contact the waste form. Closure of the repository is desired 50 years after first waste is emplaced. Both backfill and a drip shields will be emplaced at closure to improve post-closure performance.

  15. Motivating adolescents to reduce their fines in a token economy.

    PubMed

    Miller, R P; Cosgrove, J M; Doke, L

    1990-01-01

    Adolescents on a 16-bed token economy ward of a state hospital were subjected to four interventions in a seven-phase experiment to reduce the number of fines they received each day. Phase I was a four-week baseline period. Phases II and III were four- and five-week periods, respectively, in which residents were awarded tickets for a weekly $10 lottery each day they were at or below a changing criterion of daily fines. In Phase IV, residents received coupons, exchangeable for money, for days with zero fines. Phase V was a return to baseline. Phase VI was a one-week period in which daily lotteries for $1 were held, with the criterion for receiving a ticket being zero fines on the previous day. Phase VII was a one-week return to baseline. No significant differences in average fines per day, number of residents meeting criteria, or mean number of zero-fine days per week were found across phases. Results are discussed in terms of amount and immediacy of reinforcement, other opportunities to gain money, possible rebelliousness of the residents against the increased aversiveness of fines, and implications for further research.

  16. A sputnik IV saga

    NASA Astrophysics Data System (ADS)

    Lundquist, Charles A.

    2009-12-01

    The Sputnik IV launch occurred on May 15, 1960. On May 19, an attempt to deorbit a 'space cabin' failed and the cabin went into a higher orbit. The orbit of the cabin was monitored and Moonwatch volunteer satellite tracking teams were alerted to watch for the vehicle demise. On September 5, 1962, several team members from Milwaukee, Wisconsin made observations starting at 4:49 a.m. of a fireball following the predicted orbit of Sputnik IV. Requests went out to report any objects found under the fireball path. An early morning police patrol in Manitowoc had noticed a metal object on a street and had moved it to the curb. Later the officers recovered the object and had it dropped off at the Milwaukee Journal. The Moonwarch team got the object and reported the situation to Moonwatch Headquarters at the Smithsonian Astrophysical Observatory. A team member flew to Cambridge with the object. It was a solid, 9.49 kg piece of steel with a slag-like layer attached to it. Subsequent analyses showed that it contained radioactive nuclei produced by cosmic ray exposure in space. The scientists at the Observatory quickly recognized that measurements of its induced radioactivity could serve as a calibration for similar measurements of recently fallen nickel-iron meteorites. Concurrently, the Observatory directorate informed government agencies that a fragment from Sputnik IV had been recovered. Coincidently, a debate in the UN Committee on Peaceful Uses of Outer Space involved the issue of liability for damage caused by falling satellite fragments. On September 12, the Observatory delivered the bulk of the fragment to the US Delegation to the UN. Two days later, the fragment was used by US Ambassador Francis Plimpton as an exhibit that the time had come to agree on liability for damage from satellite debris. He offered the Sputnik IV fragment to USSR Ambassador P.D. Morozov, who refused the offer. On October 23, Drs. Alla Massevitch and E.K. Federov of the USSR visited the

  17. A Mn(IV)/Fe(IV) Intermediate in Assembly of the Mn(IV)/Fe(III) Cofactor of Chlamydia trachomatis Ribonucleotide Reductase†

    PubMed Central

    Jiang, Wei; Hoffart, Lee M.; Krebs, Carsten; Bollinger, J. Martin

    2008-01-01

    We recently showed that the class Ic ribonucleotide reductase from the human pathogen, Chlamydia trachomatis, uses a MnIV/FeIII cofactor to generate protein and substrate radicals in its catalytic mechanism [Jiang, W., Yun, D., Saleh, L., Barr, E. W., Xing, G., Hoffart, L. M., Maslak, M.-A., Krebs, C., and Bollinger, J. M., Jr. (2007) Science 316, 1188-1191]. Here, we have dissected the mechanism of formation of this novel heterobinuclear redox cofactor from the MnII/FeII cluster and O2. An intermediate with a g = 2 EPR signal that shows hyperfine coupling to both 55Mn and 57Fe accumulates almost quantitatively in a second order reaction between O2 and the reduced R2 complex. The otherwise slow decay of the intermediate to the active MnIV/FeIII-R2 complex is accelerated by the presence of the one-electron reductant, ascorbate, implying that the intermediate is more oxidized than MnIV/FeIII. Mössbauer spectra show that the intermediate contains a high-spin FeIV center. Its chemical and spectroscopic properties establish that the intermediate is a MnIV/FeIV-R2 complex with an S = 1/2 electronic ground state arising from antiferromagnetic coupling between the MnIV (SMn = 3/2) and high-spin FeIV (SFe = 2) sites. PMID:17616152

  18. PMD IVS Analysis Center

    NASA Technical Reports Server (NTRS)

    Tornatore, Vincenza

    2013-01-01

    The main activities carried out at the PMD (Politecnico di Milano DIIAR) IVS Analysis Center during 2012 are briefly higlighted, and future plans for 2013 are sketched out. We principally continued to process European VLBI sessions using different approaches to evaluate possible differences due to various processing choices. Then VLBI solutions were also compared to the GPS ones as well as the ones calculated at co-located sites. Concerning the observational aspect, several tests were performed to identify the most suitable method to achieve the highest possible accuracy in the determination of GNSS (GLOBAL NAVIGATION SATELLITE SYSTEM) satellite positions using the VLBI technique.

  19. Washability of fine coal

    SciTech Connect

    Cavallaro, J.A.

    1984-01-01

    The objectives of this study are: (1) to determine the theoretical beneficiation potential of US coals when pulverized down to 44 microns, (2) to determine the effects of fine grinding on the liberation of ash, pyritic sulfur, and other impurities, and (3) to assess the impact of their removal on oil and gas replacement, environmental regulations, and specification feedstocks for emerging coal utilization technologies. With the emphasis on fine coal cleaning, we have developed a centrifugal float-sink technique for coals crushed down to 44 microns. Employing this technique will provide a complete fine coal gravimetric evaluation of US coals crushed down to 44 microns. Parallel research is being conducted through in-house studies by PETC, and contracts with the University of Alaska, the University of North Dakota, and Commercial Testing and Engineering, Inc. Results thus far have been encouraging for selected Northern Appalachian Region Coals (NAR), which have shown pyritic sulfur, SO/sub 2/ emission, and ash reductions of 94, 60, and 82%, respectively, for the float 1.30 specific gravity product. However, the data evaluated for several samples indicate a possible problem in the yield/ash relationship for the float 1.30 specific gravity products for samples crushed to 75 and 44 microns top size. Thus, testing was begun to try to resolve these anomalies in the data. Test results using surface active agents, a reverse order of float-sink, and sample pre-heat techniques have been promising. These modifications to the standard technique resulted in an increase in weight recovery of float 1.30 specific gravity material and a decrease in ash content for each of the other specific gravity fractions, thus showing an improvement in the yield/ash relationship.

  20. Very fine Twilights

    NASA Astrophysics Data System (ADS)

    Boico, Vladimir

    1992-04-01

    The author is describing a very fine twilight on 3 January 1992 at 17 h25 m LT (The Sunset was at 16h48m LT) of red - terracotta color. The author is relating this twilight with the volcanic erruption of Pinatubo on the Philipines islands from June 1991. The author is describing the following phenomena related with Volcanic erruption: twilights, the greenish of the Moon's surface, a change in the color of Day Sky to white, Haloes around the Sun. The author is pointing out, that the phenomena mentioned could prolonge in time 2 or 3 years.

  1. Fine needle aspiration cytology.

    PubMed Central

    Lever, J V; Trott, P A; Webb, A J

    1985-01-01

    Fine needle aspiration cytology is an inexpensive, atraumatic technique for the diagnosis of disease sites. This paper describes the technique and illustrates how it may be applied to the management of tumours throughout the body. The limitations of the method, the dangers of false positive reports, and the inevitability of false negative diagnoses are emphasised. In a clinical context the method has much to offer by saving patients from inappropriate operations and investigations and allowing surgeons to plan quickly and more rationally. It is an economically valuable technique and deserves greater recognition. Images PMID:2578481

  2. Finessing fuel fineness

    SciTech Connect

    Storm, R.F.

    2008-10-15

    Most of today's operating coal plants began service at least a generation ago and were designed to burn eastern bituminous coal. A switch to Powder River Basin coal can stress those plants' boiler systems, especially the pulverisers, beyond their design limits and cause no end of operational and maintenance problems. Many of those problems are caused by failing to maintain good fuel fineness when increasing fuel throughput. This article concerns the proper management of the fuel component of the combustion equation in an eight step plan. 8 figs.

  3. Division Iv: Stars

    NASA Astrophysics Data System (ADS)

    Corbally, Christopher; D'Antona, Francesca; Spite, Monique; Asplund, Martin; Charbonnel, Corinne; Docobo, Jose Angel; Gray, Richard O.; Piskunov, Nikolai E.

    2012-04-01

    This Division IV was started on a trial basis at the General Assembly in The Hague 1994 and was formally accepted at the Kyoto General Assembly in 1997. Its broad coverage of ``Stars'' is reflected in its relatively large number of Commissions and so of members (1266 in late 2011). Its kindred Division V, ``Variable Stars'', has the same history of its beginning. The thinking at the time was to achieve some kind of balance between the number of members in each of the 12 Divisions. Amid the current discussion of reorganizing the number of Divisions into a more compact form it seems advisable to make this numerical balance less of an issue than the rationalization of the scientific coverage of each Division, so providing more effective interaction within a particular field of astronomy. After all, every star is variable to a certain degree and such variability is becoming an ever more powerful tool to understand the characteristics of every kind of normal and peculiar star. So we may expect, after hearing the reactions of members, that in the restructuring a single Division will result from the current Divisions IV and V.

  4. Fine Channel Networks

    NASA Technical Reports Server (NTRS)

    1997-01-01

    A color image of fine channel networks on Mars; north toward top. The scene shows heavily cratered highlands dissected by dendritic open channel networks that dissect steep slopes of impact crater walls. This image is a composite of Viking high-resolution images in black and white and low-resolution images in color. The image extends from latitude 9 degrees S. to 5 degrees S. and from longitude 312 degrees to 320 degrees; Mercator projection. The dendritic pattern of the fine channels and their location on steep slopes leads to the interpretation that these are runoff channels. The restriction of these types of channels to ancient highland rocks suggests that these channels are old and date from a time on Mars when conditions existed for precipitation to actively erode rocks. After the channels reach a low plain, they appear to end. Termination may have resulted from burial by younger deposits or perhaps the flows percolated into the surface materials and continued underground.

  5. Fine Channel Networks

    NASA Technical Reports Server (NTRS)

    1997-01-01

    A color image of fine channel networks on Mars; north toward top. The scene shows heavily cratered highlands dissected by dendritic open channel networks that dissect steep slopes of impact crater walls. This image is a composite of Viking high-resolution images in black and white and low-resolution images in color. The image extends from latitude 9 degrees S. to 5 degrees S. and from longitude 312 degrees to 320 degrees; Mercator projection. The dendritic pattern of the fine channels and their location on steep slopes leads to the interpretation that these are runoff channels. The restriction of these types of channels to ancient highland rocks suggests that these channels are old and date from a time on Mars when conditions existed for precipitation to actively erode rocks. After the channels reach a low plain, they appear to end. Termination may have resulted from burial by younger deposits or perhaps the flows percolated into the surface materials and continued underground.

  6. Injection with ultra-fine cement into fine sand layer

    SciTech Connect

    Tamura, Masahito; Goto, Toshiyoshi; Ogino, Takuya; Shimizu, Kazunari

    1994-12-31

    In-situ injection test was carried out in fine sand layer with ordinary portland, colloid and ultra-fine cement. Permeability of the sand layer was 10{sup {minus}3} cm/sec. Suspension grout with ordinary portland and colloid cement was impossible to permeate into the sand. However with ultra fine cement small solidified sand was obtained and with ultra-fine cement-waterglass grout, water cement ratio of 0.8 and waterglass concentration of 75%, solidified sand with expected volume can be obtained.

  7. The relationship between aerosol particles chemical composition and optical properties to identify the biomass burning contribution to fine particles concentration: a case study for São Paulo city, Brazil.

    PubMed

    de Miranda, Regina Maura; Lopes, Fabio; do Rosário, Nilton Évora; Yamasoe, Marcia Akemi; Landulfo, Eduardo; de Fatima Andrade, Maria

    2016-12-01

    The air quality in the Metropolitan Area of São Paulo (MASP) is primarily determined by the local pollution source contribution, mainly the vehicular fleet, but there is a concern about the role of remote sources to the fine mode particles (PM2.5) concentration and composition. One of the most important remote sources of atmospheric aerosol is the biomass burning emissions from São Paulo state's inland and from the central and north portions of Brazil. This study presents a synergy of different measurements of atmospheric aerosol chemistry and optical properties in the MASP in order to show how they can be used as a tool to identify particles from local and remote sources. For the clear identification of the local and remote source contribution, aerosol properties measurements at surface level were combined with vertical profiles information. Over 15 days in the austral winter of 2012, particulate matter (PM) was collected using a cascade impactor and a Partisol sampler in São Paulo City. Mass concentrations were determined by gravimetry, black carbon concentrations by reflectance, and trace element concentrations by X-ray fluorescence. Aerosol optical properties were studied using a multifilter rotating shadowband radiometer (MFRSR), a Lidar system and satellite data. Optical properties, concentrations, size distributions, and elemental composition of atmospheric particles were strongly related and varied according to meteorological conditions. During the sampling period, PM mean mass concentrations were 17.4 ± 10.1 and 15.3 ± 6.9 μg/m(3) for the fine and coarse fractions, respectively. The mean aerosol optical depths at 415 nm and Ångström exponent (AE) over the whole period were 0.29 ± 0.14 and 1.35 ± 0.11, respectively. Lidar ratios reached values of 75 sr. The analyses of the impacts of an event of biomass burning smoke transport to the São Paulo city revealed significant changing on local aerosol concentrations and optical parameters

  8. 78 FR 2390 - CSOLAR IV South, LLC, Wistaria Ranch Solar, LLC, CSOLAR IV West, LLC, CSOLAR IV North, LLC v...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-01-11

    ... Energy Regulatory Commission CSOLAR IV South, LLC, Wistaria Ranch Solar, LLC, CSOLAR IV West, LLC, CSOLAR IV North, LLC v. California Independent System Operator Corporation; Notice of Complaint Take notice... IV South, LLC, Wistaria Ranch Solar, LLC, CSOLAR IV West, LLC and CSOLAR IV North, LLC (collectively...

  9. Fine sediments suppress detritivory on coral reefs.

    PubMed

    Tebbett, Sterling B; Goatley, Christopher H R; Bellwood, David R

    2017-01-30

    Increasing sediment inputs are recognised as an important factor leading to coral reef degradation. However, the role of sediments in ecological processes is poorly understood. This study used paired-choice trials to quantify the effects of sediment grain size and chemical composition on feeding by the abundant detritivorous reef fish, Ctenochaetus striatus. The size of sediments from algal turfs were also compared to those ingested by reef-dwelling C. striatus. Algal turfs containing coarser sediments were preferred by C. striatus, while sediment composition (reefal carbonates vs. riverine silicates) had little effect. On the reef, C. striatus ingested finer sediments than those present in algal turfs. C. striatus appears to prefer algal turfs with coarser sediments as this facilitates ingestion of fine detrital particles, while finer sediments prevent selective feeding on detritus. These findings suggest that fine sediments from terrestrial runoff or dredging may be detrimental to feeding by detritivorous species.

  10. Granulation of fine powder

    DOEpatents

    Chen, Ching-Fong

    2016-08-09

    A mixture of fine powder including thorium oxide was converted to granulated powder by forming a first-green-body and heat treating the first-green-body at a high temperature to strengthen the first-green-body followed by granulation by crushing or milling the heat-treated first-green-body. The granulated powder was achieved by screening through a combination of sieves to achieve the desired granule size distribution. The granulated powder relies on the thermal bonding to maintain its shape and structure. The granulated powder contains no organic binder and can be stored in a radioactive or other extreme environment. The granulated powder was pressed and sintered to form a dense compact with a higher density and more uniform pore size distribution.

  11. Radiology and fine art.

    PubMed

    Marinković, Slobodan; Stošić-Opinćal, Tatjana; Tomić, Oliver

    2012-07-01

    The radiologic aesthetics of some body parts and internal organs have inspired certain artists to create specific works of art. Our aim was to describe the link between radiology and fine art. We explored 13,625 artworks in the literature produced by 2049 artists and found several thousand photographs in an online image search. The examination revealed 271 radiologic artworks (1.99%) created by 59 artists (2.88%) who mainly applied radiography, sonography, CT, and MRI. Some authors produced radiologic artistic photographs, and others used radiologic images to create artful compositions, specific sculptures, or digital works. Many radiologic artworks have symbolic, metaphoric, or conceptual connotations. Radiology is clearly becoming an original and important field of modern art.

  12. Automated Camera Array Fine Calibration

    NASA Technical Reports Server (NTRS)

    Clouse, Daniel; Padgett, Curtis; Ansar, Adnan; Cheng, Yang

    2008-01-01

    Using aerial imagery, the JPL FineCalibration (JPL FineCal) software automatically tunes a set of existing CAHVOR camera models for an array of cameras. The software finds matching features in the overlap region between images from adjacent cameras, and uses these features to refine the camera models. It is not necessary to take special imagery of a known target and no surveying is required. JPL FineCal was developed for use with an aerial, persistent surveillance platform.

  13. The BALDER Beamline at the MAX IV Laboratory

    NASA Astrophysics Data System (ADS)

    Klementiev, K.; Norén, K.; Carlson, S.; Sigfridsson Clauss, K. G. V.; Persson, I.

    2016-05-01

    X-ray absorption spectroscopy (XAS) includes well-established methods to study the local structure around the absorbing element - extended X-ray absorption fine structure (EXAFS), and the effective oxidation number or to quantitatively determine the speciation of an element in a complex matrix - X-ray absorption near-edge structure (XANES). The increased brilliance and intensities available at the new generation of synchrotron light sources makes it possible to study, in-situ and in-operando, much more dilute systems with relevance for natural systems, as well as the micro-scale variability and dynamics of chemical reactions on the millisecond time-scale. The design of the BALDER beamline at the MAX IV Laboratory 3 GeV ring has focused on a high flux of photons in a wide energy range, 2.4-40 keV, where the K-edge is covered for the elements S to La, and the L 3-edge for all elements heavier than Sb. The overall design of the beamline will allow large flexibility in energy range, beam size and data collection time. The other focus of the beamline design is the possibility to perform multi-technique analyses on samples. Development of sample environment requires focus on implementation of auxiliary methods in such a way that techniques like Fourier transform infrared (FTIR) spectroscopy, UV-Raman spectroscopy, X-ray diffraction and/or mass spectrometry can be performed simultaneously as the XAS study. It will be a flexible system where different instruments can be plugged in and out depending on the needs for the particular investigation. Many research areas will benefit from the properties of the wiggler based light source and the capabilities to perform in-situ and in-operando measurements, for example environmental and geochemical sciences, nuclear chemistry, catalysis, materials sciences, and cultural heritage.

  14. dBASE IV basics

    SciTech Connect

    O`Connor, P.

    1994-09-01

    This is a user`s manual for dBASE IV. dBASE IV is a popular software application that can be used on your personal computer to help organize and maintain your database files. It is actually a set of tools with which you can create, organize, select and manipulate data in a simple yet effective manner. dBASE IV offers three methods of working with the product: (1) control center: (2) command line; and (3) programming.

  15. Continuous fine ash depressurization system

    DOEpatents

    Liu, Guohai [Birmingham, AL; Peng, Wan Wang [Birmingham, AL; Vimalchand, Pannalal [Birmingham, AL

    2011-11-29

    A system for depressurizing and cooling a high pressure, high temperature fine solid particles stream having entrained gas therein. In one aspect, the system has an apparatus for cooling the high pressure, high temperature fine solid particles stream having entrained gas therein and a pressure letdown device for depressurization by separating the cooled fine solid particles from a portion of the fine solid particles stream having entrained gas therein, resulting in a lower temperature, lower pressure outlet of solid particles for disposal or handling by downstream equipment.

  16. Improving IV-A/IV-D Interface. Handbook.

    ERIC Educational Resources Information Center

    National Inst. for Child Support Enforcement, Chevy Chase, MD.

    Effective interface between the Aid to Families with Dependent Children (IV-A) and the Child Support Enforcement (IV-D) programs is a key factor in assisting families in becoming self-sufficient, reducing welfare expenditures, and enforcing parental responsibility to support their children. Consequently, overcoming the procedural, technological,…

  17. Improving IV-A/IV-D Interface. Trainer Guide.

    ERIC Educational Resources Information Center

    National Inst. for Child Support Enforcement, Chevy Chase, MD.

    Effective interface between the Aid to Families with Dependent Children (IV-A) and the Child Support Enforcement (IV-D) programs is a key factor in assisting families in becoming self-sufficient, reducing welfare expenditures, and enforcing parental responsibility to support their children. Consequently, overcoming the procedural, technological,…

  18. Confirmatory Factor Analysis of the WAIS-IV/WMS-IV

    ERIC Educational Resources Information Center

    Holdnack, James A.; Zhou, Xiaobin; Larrabee, Glenn J.; Millis, Scott R.; Salthouse, Timothy A.

    2011-01-01

    The Wechsler Adult Intelligence Scale-fourth edition (WAIS-IV) and the Wechsler Memory Scale-fourth edition (WMS-IV) were co-developed to be used individually or as a combined battery of tests. The independent factor structure of each of the tests has been identified; however, the combined factor structure has yet to be determined. Confirmatory…

  19. Confirmatory Factor Analysis of the WAIS-IV/WMS-IV

    ERIC Educational Resources Information Center

    Holdnack, James A.; Zhou, Xiaobin; Larrabee, Glenn J.; Millis, Scott R.; Salthouse, Timothy A.

    2011-01-01

    The Wechsler Adult Intelligence Scale-fourth edition (WAIS-IV) and the Wechsler Memory Scale-fourth edition (WMS-IV) were co-developed to be used individually or as a combined battery of tests. The independent factor structure of each of the tests has been identified; however, the combined factor structure has yet to be determined. Confirmatory…

  20. Gen IV Materials Handbook Implementation Plan

    SciTech Connect

    Rittenhouse, P.; Ren, W.

    2005-03-29

    A Gen IV Materials Handbook is being developed to provide an authoritative single source of highly qualified structural materials information and materials properties data for use in design and analyses of all Generation IV Reactor Systems. The Handbook will be responsive to the needs expressed by all of the principal government, national laboratory, and private company stakeholders of Gen IV Reactor Systems. The Gen IV Materials Handbook Implementation Plan provided here addresses the purpose, rationale, attributes, and benefits of the Handbook and will detail its content, format, quality assurance, applicability, and access. Structural materials, both metallic and ceramic, for all Gen IV reactor types currently supported by the Department of Energy (DOE) will be included in the Gen IV Materials Handbook. However, initial emphasis will be on materials for the Very High Temperature Reactor (VHTR). Descriptive information (e.g., chemical composition and applicable technical specifications and codes) will be provided for each material along with an extensive presentation of mechanical and physical property data including consideration of temperature, irradiation, environment, etc. effects on properties. Access to the Gen IV Materials Handbook will be internet-based with appropriate levels of control. Information and data in the Handbook will be configured to allow search by material classes, specific materials, specific information or property class, specific property, data parameters, and individual data points identified with materials parameters, test conditions, and data source. Details on all of these as well as proposed applicability and consideration of data quality classes are provided in the Implementation Plan. Website development for the Handbook is divided into six phases including (1) detailed product analysis and specification, (2) simulation and design, (3) implementation and testing, (4) product release, (5) project/product evaluation, and (6) product

  1. Dewatering studies of fine clean coal

    SciTech Connect

    Parekh, B.K.

    1991-01-01

    The main objective of the present research program is to study and understand dewatering characteristics of ultrafine clean coal obtained using the advanced column flotation technique from the Kerr-McGee's Galatia preparation plant fine coal waste stream. It is also the objective of the research program to utilize the basic study results, i.e., surface chemical, particle shape particle size distribution, etc., in developing a cost-effective dewatering method. The ultimate objective is to develop process criteria to obtain a dewatered clean coal product containing less that 20 percent moisture, using the conventional vacuum dewatering equipment. (VC)

  2. Manufacture of finely divided carbon

    SciTech Connect

    Walker, D.G.

    1980-01-22

    Finely divided carbon is manufactured by a process producing a gaseous stream containing carbon monoxide by reacting coal and air in a slagging ash gasifier, separating carbon monoxide from the gaseous mixture, and disproportionating the carbon monoxide to produce finely divided carbon and carbon dioxide, the latter of which is recycled to the gasifier.

  3. Chemical characterization of outdoor and subway fine (PM(2.5-1.0)) and coarse (PM(10-2.5)) particulate matter in Seoul (Korea) by computer-controlled scanning electron microscopy (CCSEM).

    PubMed

    Byeon, Sang-Hoon; Willis, Robert; Peters, Thomas M

    2015-02-13

    Outdoor and indoor (subway) samples were collected by passive sampling in urban Seoul (Korea) and analyzed with computer-controlled scanning electron microscopy coupled with energy dispersive x-ray spectroscopy (CCSEM-EDX). Soil/road dust particles accounted for 42%-60% (by weight) of fine particulate matter larger than 1 µm (PM(2.5-1.0)) in outdoor samples and 18% of PM2.5-1.0 in subway samples. Iron-containing particles accounted for only 3%-6% in outdoor samples but 69% in subway samples. Qualitatively similar results were found for coarse particulate matter (PM(10-2.5)) with soil/road dust particles dominating outdoor samples (66%-83%) and iron-containing particles contributing most to subway PM(10-2.5) (44%). As expected, soil/road dust particles comprised a greater mass fraction of PM(10-2.5) than PM(2.5-1.0). Also as expected, the mass fraction of iron-containing particles was substantially less in PM(10-2.5) than in PM(2.5-1.0). Results of this study are consistent with known emission sources in the area and with previous studies, which showed high concentrations of iron-containing particles in the subway compared to outdoor sites. Thus, passive sampling with CCSEM-EDX offers an inexpensive means to assess PM(2.5-1.0) and PM(10-2.5) simultaneously and by composition at multiple locations.

  4. NATIONAL COASTAL CONDITION REPORT IV

    EPA Science Inventory

    The National Coastal Condition Report IV (NCCR IV) is the fourth in a series of environmental assessments of U.S. coastal waters and the Great Lakes. The report includes assessments of all the nation’s estuaries in the contiguous 48 states and Puerto Rico, south-eastern Alaska, ...

  5. NATIONAL COASTAL CONDITION REPORT IV

    EPA Science Inventory

    The National Coastal Condition Report IV (NCCR IV) is the fourth in a series of environmental assessments of U.S. coastal waters and the Great Lakes. The report includes assessments of all the nation’s estuaries in the contiguous 48 states and Puerto Rico, south-eastern Alaska, ...

  6. Degradation of type IV collagen by neoplastic human skin fibroblasts

    SciTech Connect

    Sheela, S.; Barrett, J.C.

    1985-02-01

    An assay for the degradation of type IV (basement membrane) collagen was developed as a biochemical marker for neoplastic cells from chemically transformed human skin fibroblasts. Type IV collagen was isolated from basement membrane of Syrian hamster lung and type I collagen was isolated from rat tails; the collagens were radioactively labelled by reductive alkylation. The abilities of normal (KD) and chemically transformed (Hut-11A) human skin fibroblasts to degrade the collagens were studied. A cell-associated assay was performed by growing either normal or transformed cells in the presence of radioactively labelled type IV collagen and measuring the released soluble peptides in the medium. This assay also demonstrated that KD cells failed to synthesize an activity capable of degrading type IV collagen whereas Hut-11A cells degraded type IV collagen in a linear manner for up to 4 h. Human serum at very low concentrations, EDTA and L-cysteine inhibited the enzyme activity, whereas protease inhibitors like phenylmethyl sulfonyl fluoride, N-ethyl maleimide or soybean trypsin inhibitor did not inhibit the enzyme from Hut-11A cells. These results suggest that the ability to degrade specifically type IV collagen may be an important marker for neoplastic human fibroblasts and supports a role for this collagenase in tumor cell invasion.

  7. Type IV Pilin Proteins: Versatile Molecular Modules

    PubMed Central

    Giltner, Carmen L.; Nguyen, Ylan

    2012-01-01

    Summary: Type IV pili (T4P) are multifunctional protein fibers produced on the surfaces of a wide variety of bacteria and archaea. The major subunit of T4P is the type IV pilin, and structurally related proteins are found as components of the type II secretion (T2S) system, where they are called pseudopilins; of DNA uptake/competence systems in both Gram-negative and Gram-positive species; and of flagella, pili, and sugar-binding systems in the archaea. This broad distribution of a single protein family implies both a common evolutionary origin and a highly adaptable functional plan. The type IV pilin is a remarkably versatile architectural module that has been adopted widely for a variety of functions, including motility, attachment to chemically diverse surfaces, electrical conductance, acquisition of DNA, and secretion of a broad range of structurally distinct protein substrates. In this review, we consider recent advances in this research area, from structural revelations to insights into diversity, posttranslational modifications, regulation, and function. PMID:23204365

  8. Chemical Characterization of Outdoor and Subway Fine (PM2.5–1.0) and Coarse (PM10–2.5) Particulate Matter in Seoul (Korea) by Computer-Controlled Scanning Electron Microscopy (CCSEM)

    PubMed Central

    Byeon, Sang-Hoon; Willis, Robert; Peters, Thomas M.

    2015-01-01

    Outdoor and indoor (subway) samples were collected by passive sampling in urban Seoul (Korea) and analyzed with computer-controlled scanning electron microscopy coupled with energy dispersive x-ray spectroscopy (CCSEM-EDX). Soil/road dust particles accounted for 42%–60% (by weight) of fine particulate matter larger than 1 µm (PM2.5–1.0) in outdoor samples and 18% of PM2.5–1.0 in subway samples. Iron-containing particles accounted for only 3%–6% in outdoor samples but 69% in subway samples. Qualitatively similar results were found for coarse particulate matter (PM10–2.5) with soil/road dust particles dominating outdoor samples (66%–83%) and iron-containing particles contributing most to subway PM10–2.5 (44%). As expected, soil/road dust particles comprised a greater mass fraction of PM10–2.5 than PM2.5–1.0. Also as expected, the mass fraction of iron-containing particles was substantially less in PM10–2.5 than in PM2.5–1.0. Results of this study are consistent with known emission sources in the area and with previous studies, which showed high concentrations of iron-containing particles in the subway compared to outdoor sites. Thus, passive sampling with CCSEM-EDX offers an inexpensive means to assess PM2.5–1.0 and PM10-2.5 simultaneously and by composition at multiple locations. PMID:25689348

  9. Aqueous complexation of thorium(IV), uranium(IV), neptunium(IV), plutonium(III/IV), and cerium(III/IV) with DTPA.

    PubMed

    Brown, M Alex; Paulenova, Alena; Gelis, Artem V

    2012-07-16

    Aqueous complexation of Th(IV), U(IV), Np(IV), Pu(III/IV), and Ce(III/IV) with DTPA was studied by potentiometry, absorption spectrophotometry, and cyclic voltammetry at 1 M ionic strength and 25 °C. The stability constants for the 1:1 complex of each trivalent and tetravalent metal were calculated. From the potentiometric data, we report stability constant values for Ce(III)DTPA, Ce(III)HDTPA, and Th(IV)DTPA of log β(101) = 20.01 ± 0.02, log β(111) = 22.0 ± 0.2, and log β(101) = 29.6 ± 1, respectively. From the absorption spectrophotometry data, we report stability constant values for U(IV)DTPA, Np(IV)DTPA, and Pu(IV)DTPA of log β(101) = 31.8 ± 0.1, 32.3 ± 0.1, and 33.67 ± 0.02, respectively. From the cyclic voltammetry data, we report stability constant values for Ce(IV) and Pu(III) of log β(101) = 34.04 ± 0.04 and 20.58 ± 0.04, respectively. The values obtained in this work are compared and discussed with respect to the ionic radius of each cationic metal.

  10. 'RAT' Leaves a Fine Mess

    NASA Technical Reports Server (NTRS)

    2004-01-01

    This graph shows the light signatures, or spectra, of two sides of the rock dubbed 'Bounce,' located at Meridiani Planum, Mars. The spectra were taken by the miniature thermal emission spectrometer on the Mars Exploration Rover Opportunity. The left side of this rock is covered by fine dust created when the rover drilled into the rock with its rock abrasion tool. These 'fines' produce a layer of pyroxene dust that can be detected here in the top spectrum. The right side of the rock has fewer fines and was used to investigate the composition of this basaltic rock.

  11. Uprated fine guidance sensor study

    NASA Technical Reports Server (NTRS)

    1984-01-01

    Future orbital observatories will require star trackers of extremely high precision. These sensors must maintain high pointing accuracy and pointing stability simultaneously with a low light level signal from a guide star. To establish the fine guidance sensing requirements and to evaluate candidate fine guidance sensing concepts, the Space Telescope Optical Telescope Assembly was used as the reference optical system. The requirements review was separated into three areas: Optical Telescope Assembly (OTA), Fine Guidance Sensing and astrometry. The results show that the detectors should be installed directly onto the focal surface presented by the optics. This would maximize throughput and minimize point stability error by not incoporating any additional optical elements.

  12. Biological and chemical investigation of Allium cepa L. response to selenium inorganic compounds.

    PubMed

    Michalska-Kacymirow, M; Kurek, E; Smolis, A; Wierzbicka, M; Bulska, E

    2014-06-01

    The aim of this study was to evaluate the biological and chemical response of Allium cepa L. exposed to inorganic selenium compounds. Besides the investigation of the total content of selenium as well as its chemical speciation, the Allium test was used to evaluate the growth of onion roots and mitotic activity in the roots' meristem. The total content of selenium was determined by inductively coupled plasma mass spectrometry (ICP MS). High-performance liquid chromatography (HPLC), coupled to ICP MS, was used for the selenium chemical speciation. Results indicated that A. cepa plants are able to biotransform inorganic selenium compounds into their organic derivatives, e.g., Se-methylselenocysteine from the Se(IV) inorganic precursor. Although the differences in the biotransformation of selenium are due mainly to the oxidation state of selenium, the experiment has also shown a fine effect of counter ions (H(+), Na(+), NH4 (+)) on the response of plants and on the specific metabolism of selenium.

  13. IV INTERNATIONAL CONFERENCE ON ATOM AND MOLECULAR PULSED LASERS (AMPL'99): Efficiency of an H2—SF6 laser with electron-beam initiation of chemical reactions

    NASA Astrophysics Data System (ADS)

    Erofeev, M. V.; Orlovskii, Viktor M.; Skakun, V. S.; Sosnin, E. A.; Tarasenko, Viktor F.

    2000-06-01

    The spectral and amplitude—time characteristics of HF lasers pumped by a nonchain chemical reaction and initiated by radially convergent and planar electron beams were investigated. The principal channels leading to the formation of vibrationally excited HF molecules were analysed. It was confirmed that high efficiencies (~10%) of a nonchain HF laser may be attained only as a result of the simultaneous formation of atomic and molecular fluorine when the active mixture is acted upon by an electron beam and of the participation of molecular fluorine in population inversion. It was shown that a laser pulse has a complex spectral—temporal profile caused by the successive generation of P-lines and the overlap during the radiation pulse of both the rotational lines of the same vibrational band and of individual vibrational bands.

  14. New fine structure cooling rate

    NASA Technical Reports Server (NTRS)

    Hoegy, W. R.

    1976-01-01

    One of the dominant electron cooling processes in the ionosphere is caused by electron impact induced fine structure transitions among the ground state levels of atomic oxygen. This fine structure cooling rate is based on theoretical cross sections. Recent advances in the numerical cross section determinations to include polarization effects and more accurate representations of the atomic target result in new lower values. These cross sections are employed in this paper to derive a new fine structure cooling rate which is between 40% and 60% of the currently used rate. A new generalized formula is presented for the cooling rate (from which the fine structure cooling rate is derived), valid for arbitrary mass and temperature difference of the colliding particles and arbitrary inelastic energy difference.

  15. Analysis of cadmium in undissolved anode materials of Mark-IV electro-refiner

    SciTech Connect

    Yoo, Tae-Sic; Fredrickson, G.L.; Vaden, D.; Westphal, B.

    2013-07-01

    The Mark-IV electro-refiner (Mk-IV ER) is a unit process in the FCF (Fuel Conditioning Facility), which is primarily assigned to treating the used driver fuels. Mk-IV ER contains an electrolyte/molten cadmium system for refining uranium electrochemically. Typically, the anode of the Mk-IV ER consists of the chopped sodium-bonded metallic driver fuels, which have been primarily U-10Zr binary fuels. Chemical analysis of the residual anode materials after electrorefining indicates that a small amount of cadmium is removed from the Mk-IV ER along with the undissolved anode materials. Investigation of chemical analysis data indicates that the amount of cadmium in the undissolved anode materials is strongly correlated with the anode rotation speeds and the residence time of the anode in the Mk-IV ER. Discussions are given to explain the prescribed correlation. (authors)

  16. Isotopic exchange in mineral-fluid systems. IV. The crystal chemical controls on oxygen isotope exchange rates in carbonate-H 2O and layer silicate-H 2O systems

    NASA Astrophysics Data System (ADS)

    Cole, David R.

    2000-03-01

    Oxygen isotope exchange between minerals and water in systems far from chemical equilibrium is controlled largely by surface reactions such as dissolution-precipitation. In many cases, this behavior can be modeled adequately by a simple pseudo-first order rate model that accounts for changes in surface area of the solid. Previous modeling of high temperature isotope exchange data for carbonates, sulfates, and silicates indicated that within a given mineral group there appears to be a systematic relationship between rate and mineral chemistry. We tested this idea by conducting oxygen isotope exchange experiments in the systems, carbonate-H 2O and layer silicate-H 2O at 300 and 350°C, respectively. Witherite (BaCO 3), strontianite (SrCO 3) and calcite (CaCO 3) were reacted with pure H 2O for different lengths of time (271-1390 h) at 300°C and 100 bars. The layer silicates, chlorite, biotite and muscovite were reacted with H 2O for durations ranging from 132 to 3282 h at 350°C and 250 bars. A detailed survey of grain sizes and grain habits using scanning electron microscopy (SEM) indicated that grain regrowth occurred in all experiments to varying extents. Changes in the mean grain diameters were particularly significant in experiments involving withertite, strontianite and biotite. The variations in the extent of oxygen isotope exchange were measured as a function of time, and fit to a pseudo-first order rate model that accounted for the change in surface area of the solid during reaction. The isotopic rates (ln r) for the carbonate-H 2O system are -20.75 ± 0.44, -18.95 ± 0.62 and -18.51 ± 0.48 mol O m -2 s -1 for calcite, strontianite and witherite, respectively. The oxygen isotope exchange rates for layer silicate-H 2O systems are -23.99 ± 0.89, -23.14 ± 0.74 and -22.40 ± 0.66 mol O m -2 s -1 for muscovite, biotite and chlorite, respectively. The rates for the carbonate-H 2O systems increase in order from calcite to strontianite to witherite. This order

  17. Discovery and structural characterisation of new fold type IV-transaminases exemplify the diversity of this enzyme fold

    PubMed Central

    Pavkov-Keller, Tea; Strohmeier, Gernot A.; Diepold, Matthias; Peeters, Wilco; Smeets, Natascha; Schürmann, Martin; Gruber, Karl; Schwab, Helmut; Steiner, Kerstin

    2016-01-01

    Transaminases are useful biocatalysts for the production of amino acids and chiral amines as intermediates for a broad range of drugs and fine chemicals. Here, we describe the discovery and characterisation of new transaminases from microorganisms which were enriched in selective media containing (R)-amines as sole nitrogen source. While most of the candidate proteins were clearly assigned to known subgroups of the fold IV family of PLP-dependent enzymes by sequence analysis and characterisation of their substrate specificity, some of them did not fit to any of these groups. The structure of one of these enzymes from Curtobacterium pusillum, which can convert d-amino acids and various (R)-amines with high enantioselectivity, was solved at a resolution of 2.4 Å. It shows significant differences especially in the active site compared to other transaminases of the fold IV family and thus indicates the existence of a new subgroup within this family. Although the discovered transaminases were not able to convert ketones in a reasonable time frame, overall, the enrichment-based approach was successful, as we identified two amine transaminases, which convert (R)-amines with high enantioselectivity, and can be used for a kinetic resolution of 1-phenylethylamine and analogues to obtain the (S)-amines with e.e.s >99%. PMID:27905516

  18. Discovery and structural characterisation of new fold type IV-transaminases exemplify the diversity of this enzyme fold.

    PubMed

    Pavkov-Keller, Tea; Strohmeier, Gernot A; Diepold, Matthias; Peeters, Wilco; Smeets, Natascha; Schürmann, Martin; Gruber, Karl; Schwab, Helmut; Steiner, Kerstin

    2016-12-01

    Transaminases are useful biocatalysts for the production of amino acids and chiral amines as intermediates for a broad range of drugs and fine chemicals. Here, we describe the discovery and characterisation of new transaminases from microorganisms which were enriched in selective media containing (R)-amines as sole nitrogen source. While most of the candidate proteins were clearly assigned to known subgroups of the fold IV family of PLP-dependent enzymes by sequence analysis and characterisation of their substrate specificity, some of them did not fit to any of these groups. The structure of one of these enzymes from Curtobacterium pusillum, which can convert d-amino acids and various (R)-amines with high enantioselectivity, was solved at a resolution of 2.4 Å. It shows significant differences especially in the active site compared to other transaminases of the fold IV family and thus indicates the existence of a new subgroup within this family. Although the discovered transaminases were not able to convert ketones in a reasonable time frame, overall, the enrichment-based approach was successful, as we identified two amine transaminases, which convert (R)-amines with high enantioselectivity, and can be used for a kinetic resolution of 1-phenylethylamine and analogues to obtain the (S)-amines with e.e.s >99%.

  19. Oscillator strengths and transition probabilities from the Breit–Pauli R-matrix method: Ne IV

    SciTech Connect

    Nahar, Sultana N.

    2014-09-15

    The atomic parameters–oscillator strengths, line strengths, radiative decay rates (A), and lifetimes–for fine structure transitions of electric dipole (E1) type for the astrophysically abundant ion Ne IV are presented. The results include 868 fine structure levels with n≤ 10, l≤ 9, and 1/2≤J≤ 19/2 of even and odd parities, and the corresponding 83,767 E1 transitions. The calculations were carried out using the relativistic Breit–Pauli R-matrix method in the close coupling approximation. The transitions have been identified spectroscopically using an algorithm based on quantum defect analysis and other criteria. The calculated energies agree with the 103 observed and identified energies to within 3% or better for most of the levels. Some larger differences are also noted. The A-values show good to fair agreement with the very limited number of available transitions in the table compiled by NIST, but show very good agreement with the latest published multi-configuration Hartree–Fock calculations. The present transitions should be useful for diagnostics as well as for precise and complete spectral modeling in the soft X-ray to infra-red regions of astrophysical and laboratory plasmas. -- Highlights: •The first application of BPRM method for accurate E1 transitions in Ne IV is reported. •Amount of atomic data (n going up to 10) is complete for most practical applications. •The calculated energies are in very good agreement with most observed levels. •Very good agreement of A-values and lifetimes with other relativistic calculations. •The results should provide precise nebular abundances, chemical evolution etc.

  20. Structural and collisional data for Mg III and Al IV

    NASA Astrophysics Data System (ADS)

    Elabidi, Haykel

    2014-10-01

    We present in this work energy levels, oscillator strengths, radiative decay rates and fine structure collision strengths for the Mg III and Al IV ions. The 11 configurations: (1s2) 2s22p6, 2s22p53l, 2s2p63l, 2s22p54l (l⩽n-1, where n is the principal quantum number), yielding the lowest 75 levels are used. The collisional data for these two ions are missing in the literature, especially the database CHIANTI, this is the principal motivation behind the present work. Calculations have been performed using the AUTOSTRUCTURE code. AUTOSTRUCTURE treats the scattering problem in the distorted wave approach. Fine structure collision strengths are calculated for a range of electron energies from 10 Ry to 240 Ry. The atomic structure data are compared to available experimental and theoretical results.

  1. Monitoring pool-tail fines

    NASA Astrophysics Data System (ADS)

    Bunte, K.; Potyondy, J. P.; Abt, S. R.; Swingle, K. W.

    2010-12-01

    Fine sediment < 2 and < 6 mm deposited in pool-tail areas of mountain streams is often measured to monitor changes in the supply of fines (e.g., by dam removal, bank erosion, or watershed effects including fires and road building) or to assess the status and trend of aquatic ecosystems. Grid counts, pebble counts, and volumetric bedmaterial samples are typically used to quantify pool-tail fines. Grid-count results exhibit a high degree of variability not only among streams and among operators, but also among crews performing a nearly identical procedure (Roper et al. 2010). Variability is even larger when diverse methods are employed, each of which quantifies fines in a different way: grid counts visually count surface fines on small patches within the pool-tail area, pebble counts pick up and tally surface particles along (riffle) transects, and volumetric samples sieve out fines from small-scale bulk samples; and even when delimited to pool-tail areas, individual methods focus on different sampling locales. Two main questions were analyzed: 1) Do pool-tail fines exhibit patterns of spatial variability and are some grid count schemes more likely to provide accurate results than others. 2) How and why does the percentage of fines vary among grid counts, pebble counts, and volumetric samples. In a field study, grids were placed at 7 locales in two rows across the wetted width of 10 pool tails in a 14-m wide 3rd order coarse gravel-bed mountain stream with <4% sand and <8% < 6 mm. Several pebble count transects were placed across each pool-tail area, and three volumetric samples were collected in each of three pool tails. Pebble and grid counts both indicated a fining trend towards one or both banks, sometimes interrupted by a secondary peak of fines within the central half of the wetted width. Among the five sampling schemes tested, grid counts covering the wetted width with 7 locales produced the highest accuracy and the least variability among the pools of the

  2. Comparison of gene expression profiles induced by coarse, fine, and ultrafile particulate matter

    EPA Science Inventory

    Coarse, fine, and ultrafine particulate matter (PM) fractions possess different physical properties and chemical compositions and may produce different adverse health effects. Studies were undertaken to determine whether or not gene expression patterns may be used to discriminate...

  3. Comparison of gene expression profiles induced by coarse, fine, and ultrafile particulate matter

    EPA Science Inventory

    Coarse, fine, and ultrafine particulate matter (PM) fractions possess different physical properties and chemical compositions and may produce different adverse health effects. Studies were undertaken to determine whether or not gene expression patterns may be used to discriminate...

  4. Interactions Between Pinus taeda (loblolly) Fine Roots and Soil Fungi: Impacts of Elevated CO2, N Availability, and Spatial Distribution of Fungi on Fine Root Persistence and Turnover

    NASA Astrophysics Data System (ADS)

    Strand, A.; Beidler, K.; McGlinn, D.; Pritchard, S. G.

    2016-12-01

    Fine root turnover represents the most significant mode of flux from plants into soil C pools. Unfortunately fine root senescence and decomposition, processes critical in turnover, are particularly understudied. For example, little is known about either the factors that influence fine-root decomposition or the fate of compounds they contain during root death. Better understanding fine root senescence and decomposition should reduce uncertainty associated with global climate models; including re-uptake of materials in dying leaves into these models has already been shown to increase their accuracy. Over 4400 individual fine-roots and 4734 rhizomorphs were tracked from initiation until disintegration over 12 years using minirhizotrons at the Duke FACE site. Image-based approaches such as minirhizotrons cannot directly assess fine-root physiological status. To assess fine-root function directly, we are now conducting manipulative experiments in P. taeda in which fine-root senescence is induced through two treatments, steam- and direct hand-girdling. Physiological status is then assessed by examining gene-expression, root anatomy and chemical composition of manipulated roots. Changing [CO2] did not change persistence times for roots, but did impact rhizomorph persistence. Both roots and rhizomorphs showed interactions between effects of N and CO2 on persistence. Most interesting is the interaction between fine-roots and rhizomorphs: fine root persistence times are reduced in the presence of rhizomorphs, but this effect depends on the amount of N available. Finally, we found experimentally inducing senescence via steam girdling to be very effective relative to hand-girdling. These results provide evidence of the importance of priming on function of soil fungi and the role of N availability on fine-root turnover. The ability to stimulate fine-root senescence provides a powerful experimental tool to examine the fates of resources contained in fine-root pools as these

  5. Hydration and hydrolysis of thorium(IV) in aqueous solution and the structures of two crystalline thorium(IV) hydrates.

    PubMed

    Torapava, Natallia; Persson, Ingmar; Eriksson, Lars; Lundberg, Daniel

    2009-12-21

    Solid octaaqua(kappa(2)O-perchlorato)thorium(IV) perchlorate hydrate, [Th(H(2)O)(8)(ClO(4))](ClO(4))(3).H(2)O, 1, and aquaoxonium hexaaquatris(kappaO-trifluoromethanesulfonato)thorium(IV) trisaquahexakis(kappaO-trifluoromethanesulfonato)thorinate(IV), H(5)O(2)[Th(H(2)O)(6)(OSO(2)CF(3))(3)][Th(H(2)O)(3)(OSO(2)CF(3))(6)], 2, were crystallized from concentrated perchloric and trifluoromethanesulfonic acid solutions, respectively. 1 adopts a severely distorted tricapped trigonal prismatic configuration with an additional oxygen from the perchlorate ion at a longer distance. 2 consists of individual hexaaquatris(kappaO-trifluoromethanesulfonato)thorium(IV) and trisaquahexakis(kappaO-trifluoromethanesulfonato)thorinate(IV) ions and an aquaoxonium ion bridging these two ions through hydrogen bonding. The hydrated thorium(IV) ion is nine-coordinated in aqueous solution as determined by extended X-ray absorption fine structure (EXAFS) and large angle X-ray scattering (LAXS). The LAXS studies also showed a second hydration sphere of about 18 water molecules, and traces of a 3rd hydration sphere. Structural studies in aqueous solution of the hydrolysis products of thorium(IV) have identified three different types of hydrolysis species: a mu(2)O-hydroxo dimer, [Th(2)(OH)(2)(H(2)O)(12)](6+), a mu(2)O-hydroxo tetramer, [Th(4)(OH)(8)(H(2)O)(16)](8+), and a mu(3)O-oxo hexamer, [Th(6)O(8)(H(2)O)(n)](8+). Detailed structures of these three hydrolysis species are given. A compilation of reported solid state structures of actinoid(IV) compounds with oxygen donor ligands show a strong correlation between the An-O bond distance and the coordination number. The earlier reported U-O bond distance in the hydrated uranium(IV) ion in aqueous solution, confirmed in this study, is related to nine-coordination. The hydrated tri- and tetravalent actinoid ions in aqueous solution all seem to be nine-coordinated. The trivalent ions show a significant difference in bond distance to prismatic and

  6. Different assembly of type IV collagen on hydrophilic and hydrophobic substrata alters endothelial cells interaction.

    PubMed

    Coelho, N Miranda; González-García, C; Planell, J A; Salmerón-Sánchez, M; Altankov, G

    2010-06-09

    Considering the structural role of type IV collagen (Col IV) in the assembly of the basement membrane (BM) and the perspective of mimicking its organization for vascular tissue engineering purposes, we studied the adsorption pattern of this protein on model hydrophilic (clean glass) and hydrophobic trichloro(octadecyl)silane (ODS) surfaces known to strongly affect the behavior of other matrix proteins. The amount of fluorescently labeled Col IV was quantified showing saturation of the surface for concentration of the adsorbing solution of about 50microg/ml, but with approximately twice more adsorbed protein on ODS. AFM studies revealed a fine - nearly single molecular size - network arrangement of Col IV on hydrophilic glass, which turns into a prominent and growing polygonal network consisting of molecular aggregates on hydrophobic ODS. The protein layer forms within minutes in a concentration-dependent manner. We further found that human umbilical vein endothelial cells (HUVEC) attach less efficiently to the aggregated Col IV (on ODS), as judged by the significantly altered cell spreading, focal adhesions formation and the development of actin cytoskeleton. Conversely, the immunofluorescence studies for integrins revealed that the fine Col IV network formed on hydrophilic substrata is better recognized by the cells via both alpha1 and alpha2 heterodimers which support cellular interaction, apart from these on hydrophobic ODS where almost no clustering of integrins was observed.

  7. Confirmatory Factor Analysis of the WAIS-IV/WMS-IV

    PubMed Central

    Holdnack, James A.; Zhou, Xiaobin; Larrabee, Glenn J.; Millis, Scott R.; Salthouse, Timothy A.

    2013-01-01

    The Wechsler Adult Intelligence Scale–fourth edition (WAIS-IV) and the Wechsler Memory Scale–fourth edition (WMS-IV) were co-developed to be used individually or as a combined battery of tests. The independent factor structure of each of the tests has been identified; however, the combined factor structure has yet to be determined. Confirmatory factor analysis was applied to the WAIS-IV/WMS-IV Adult battery (i.e., age 16-69 years) co-norming sample (n = 900) to test 13 measurement models. The results indicated that two models fit the data equally well. One model is a seven-factor solution without a hierarchical general ability factor: Verbal Comprehension, Perceptual Reasoning, Processing Speed, Auditory Working Memory, Visual Working Memory, Auditory Memory, and Visual Memory. The second model is a five-factor model composed of Verbal Comprehension, Perceptual Reasoning, Processing Speed, Working Memory, and Memory with a hierarchical general ability factor. Interpretative implications for each model are discussed. PMID:21208975

  8. Confirmatory factor analysis of the WAIS-IV/WMS-IV.

    PubMed

    Holdnack, James A; Xiaobin Zhou; Larrabee, Glenn J; Millis, Scott R; Salthouse, Timothy A

    2011-06-01

    The Wechsler Adult Intelligence Scale-fourth edition (WAIS-IV) and the Wechsler Memory Scale-fourth edition (WMS-IV) were co-developed to be used individually or as a combined battery of tests. The independent factor structure of each of the tests has been identified; however, the combined factor structure has yet to be determined. Confirmatory factor analysis was applied to the WAIS-IV/WMS-IV Adult battery (i.e., age 16-69 years) co-norming sample (n = 900) to test 13 measurement models. The results indicated that two models fit the data equally well. One model is a seven-factor solution without a hierarchical general ability factor: Verbal Comprehension, Perceptual Reasoning, Processing Speed, Auditory Working Memory, Visual Working Memory, Auditory Memory, and Visual Memory. The second model is a five-factor model composed of Verbal Comprehension, Perceptual Reasoning, Processing Speed, Working Memory, and Memory with a hierarchical general ability factor. Interpretative implications for each model are discussed.

  9. The MAX IV imaging concept.

    PubMed

    Matěj, Zdeněk; Mokso, Rajmund; Larsson, Krister; Hardion, Vincent; Spruce, Darren

    2017-01-01

    The MAX IV Laboratory is currently the synchrotron X-ray source with the beam of highest brilliance. Four imaging beamlines are in construction or in the project phase. Their common characteristic will be the high acquisition rates of phase-enhanced images. This high data flow will be managed at the local computing cluster jointly with the Swedish National Computing Infrastructure. A common image reconstruction and analysis platform is being designed to offer reliable quantification of the multidimensional images acquired at all the imaging beamlines at MAX IV.

  10. The many measures of fine particles

    SciTech Connect

    Kaye, B.H.; Trottier, R.

    1995-04-01

    Particle size is a critical parameter for a variety of operations in the chemical process industries (CPI). For example, the flow characteristics of granular materials, the sintering behavior of metallurgical powders, and the combustion efficiency of powdered coal are influenced to a major extent by particle size. The big push in the ceramics industry today is toward processing of powders at or below the one-micrometer level because use of such fine-grained materials allows tighter control of product properties. Accurate measurement or estimation of particle size is important because the quality and performance of most powder-based products are closely related to the size distribution of the fine particles. The electro-optic data processing revolution has spawned a new generation of particle-characterization equipment based on laser probing of particles systems. Computer-aided analysis of the data has come to play a dominant role. The paper discusses the critical step of sampling, the use of sieving for larger particles, the significance of particle shape, the use of lasers in size classifiers, particle surface properties, permeability techniques, and the need for instrument calibration.

  11. Settling classes for fine suspended particles

    NASA Astrophysics Data System (ADS)

    Brach-Papa, Christophe; Boyer, Patrick; Ternat, Fabien; Amielh, Muriel; Anselmet, Fabien

    2006-08-01

    The modelling of pollutant transfer in freshwater systems can be refined by considering the heterogeneities of the sedimentary dynamics and of the chemical reactivities of fine suspended particles. One of the first steps is the fractionation of these fine particles into effective settling classes. Although several methods exist, most of them are based on either granulometric considerations and/or arbitrary threshold criteria. This article presents the bases of an experimental method focusing on the direct measurement of the settling velocities without considering the granulometry and/nor any threshold criteria. The experimental work consists in recording the temporal evolution of the vertical distribution of the suspended solid concentration in a settling tank. A mathematical analysis provides the number of particle groups, and the mass contribution and the settling velocity for each This procedure is described and applied for validation, as a first step, to calibrated suspensions. Additional work is needed for a further analysis of the physical constraints involved in the model, as well as for more extensive experimental validation. To cite this article: C. Brach-Papa et al., C. R. Mecanique 334 (2006).

  12. Contribution of alpha3(IV)alpha4(IV)alpha5(IV) Collagen IV to the Mechanical Properties of the Glomerular Basement Membrane

    NASA Astrophysics Data System (ADS)

    Gyoneva, Lazarina

    The glomerular basement membrane (GBM) is a vital part of the blood-urine filtration barrier in the kidneys. In healthy GBMs, the main tension-resisting component is alpha3(IV)alpha4(IV)alpha5(IV) type IV collagen, but in some diseases it is replaced by other collagen IV isoforms. As a result, the GBM becomes leaky and disorganized, ultimately resulting in kidney failure. Our goal is to understanding the biomechanical aspects of the alpha3(IV)alpha4(IV)alpha5(IV) chains and how their absence could be responsible for (1) the initial injury to the GBM and (2) progression to kidney failure. A combination of experiments and computational models were designed for that purpose. A model basement membrane was used to compare experimentally the distensibility of tissues with the alpha3(IV)alpha4(IV)alpha5(IV) chains present and missing. The experiments showed basement membranes containing alpha3(IV)alpha4(IV)alpha5(IV) chains were less distensible. It has been postulated that the higher level of lateral cross-linking (supercoiling) in the alpha3(IV)alpha4(IV)alpha5(IV) networks contributes additional strength/stability to basement membranes. In a computational model of supercoiled networks, we found that supercoiling greatly increased the stiffness of collagen IV networks but only minimally decreased the permeability, which is well suited for the needs of the GBM. It is also known that the alpha3(IV)alpha4(IV)alpha5(IV) networks are more protected from enzymatic degradation, and we explored their significance in GBM remodeling. Our simulations showed that the more protected network was needed to prevent the system from entering a dangerous feedback cycle due to autoregulation mechanisms in the kidneys. Overall, the work adds to the evidence of biomechanical differences between the alpha3(IV)alpha4(IV)alpha5(IV) networks and other collagen IV networks, points to supercoiling as the main source of biomechanical differences, discusses the suitability of alpha3(IV)alpha4(IV

  13. Fine-grained aggregates in L3 chondrites

    NASA Astrophysics Data System (ADS)

    Watanabe, S.; Kitamura, M.; Morimoto, N.

    1987-12-01

    The textures and chemical compositions of the constituent minerals of the fine-grained aggregates (FGAs) of L3 chondrites were studied by the backscattered electron image technique, electron probe microanalysis, and transmission electron microscopy. Plagioclase and glass in the interstices between fine grains of olivine and pyroxene indicate that the FGAs once partly melted. Compositional zoning and decomposition texture of pyroxenes are similar to those observed in chondrules, indicating a common cooling history of the FGAs and chondrules. Therefore, the mechanism that caused melting of the FGAs is considered to be the same as for chondrules. Bulk compositions of the FGAs are within the range of those of chondrules, so some chondrules probably were produced by complete melting of the same precursor materials as those of the FGAs. The precursor materials must have included fine olivine and other grains that probably are condensates.

  14. On the use of speciation techniques and ab initio modelling to understand tetravalent actinide behavior in a biological medium: An(IV)DTPA case.

    PubMed

    Aupiais, J; Bonin, L; Den Auwer, C; Moisy, P; Siberchicot, B; Topin, S

    2016-03-07

    In the case of an accidental nuclear event, contamination of human bodies by actinide elements may occur. Such elements have the particularity to exhibit both radiological and chemical toxicities that may induce severe damages at several levels, depending on the biokinetics of the element. In order to eliminate the actinide elements before they are stored in target organs (liver, kidneys, or bone, depending on the element), sequestering agents must be quickly injected. However, to date, there is still no ideal sequestering agent, despite the recent interest in this topic due to contamination concerns. DTPA (diethylene triamine pentaacetic acid) is currently generating interest for the development of oral or alternative self-administrable forms. Although biokinetics data are mostly available, molecular scale characterization of actinide-DTPA complexes is still scarce. Nevertheless, strong interest is growing in the characterization of An(IV)DTPA(-) complexes at the molecular level because this opens the way for predicting the stability constants of unknown systems or even for developing new analytical strategies aimed at better and more selective decorporation. For this purpose, Extended X-ray Absorption Fine Structure (EXAFS) and Ab Initio Molecular Dynamics (AIMD) investigations were undertaken and compared with capillary electrophoresis (CE) used in a very unusual way. Indeed, it is commonly believed that CE is incapable of extracting structural information. In capillary electrophoresis, the electrophoretic mobility of an ion is a function of its charge and size. Despite very similar ratios, partial separations between An(IV)DTPA(-) species (An(IV) = Th, U, Np, Pu) were obtained. A linear relationship between the electrophoretic mobility and the actinide--oxygen distance calculated by AIMD was evidenced. As an example, the interpolated U-O distances in U(IV)DTPA(-) from CE-ICPMS experiments, EXAFS, AIMD, and the relationship between the stability constants and

  15. Title IV: Improving Indian Education.

    ERIC Educational Resources Information Center

    Barker, Kipp A.

    The Indian Education Act of 1972, Title IV, has improved Native American education by emphasizing Native American control; it comes after 400 years of Euro-American involvement in Indian education during which assimilation was the primary goal. In 1568 Jesuit priests began "civilizing" and Christianizing the "savage" Indians;…

  16. The PLATO IV Communications System.

    ERIC Educational Resources Information Center

    Sherwood, Bruce Arne; Stifle, Jack

    The PLATO IV computer-based educational system contains its own communications hardware and software for operating plasma-panel graphics terminals. Key echoing is performed by the central processing unit: every key pressed at a terminal passes through the entire system before anything appears on the terminal's screen. Each terminal is guaranteed…

  17. Radiation Monitor,IV-TEPC

    NASA Image and Video Library

    2012-12-30

    View of radiation monitor,Intra-Vehicular Tissue Equivalent Proportional Counter (IV-TEPC),relocated to NOD2 P3,Part Number (P/N): SEG33120960-301,Serial Number (S/N): 1002,in the Node 2. Photo was taken during Expedition 34.

  18. Fine Particle Scrubbing: A Proceedings

    ERIC Educational Resources Information Center

    Journal of the Air Pollution Control Association, 1974

    1974-01-01

    These articles deal with the proceedings of a 1974 symposium on the use of wet scrubbers for the control of fine particle air pollutants. Various wet scrubbers, their engineering, performance, efficiency, and future are discussed. Tables, formulas, and models are included. (TK)

  19. Fine structure in krypton excimer

    SciTech Connect

    Hemici, M.; Saoudi, R.; Descroix, E.; Audouard, E.; Laporte, P. ); Spiegelmann, F. )

    1995-04-01

    By using laser reduced fluorescence techniques, molecular absorption from the first relaxed excited excimer states of krypton is obtained in the 960--990-nm wavelength range. Five bands are observed and analyzed by comparison with an [ital ab] [ital initio] calculated spectrum. The fine structure is thus evidenced.

  20. Fine Arts. [SITE 2002 Section].

    ERIC Educational Resources Information Center

    Robin, Bernard, Ed.

    This document contains two papers on fine arts from the SITE (Society for Information Technology & Teacher Education) 2002 conference. "Expanding the Boundaries of the Music Education of the Elementary Teacher Classroom with Information Technology" (Cheryl Jackson) reports on how information technology is used in a music methods…

  1. Regional Background Fine Particulate Matter

    EPA Science Inventory

    A modeling system composed of the global model GEOS-Chem providing hourly lateral boundary conditions to the regional model CMAQ was used to calculate the policy relevant background level of fine particulate: matter. Simulations were performed for the full year of 2004 over the d...

  2. Fine Arts Education. Research Brief

    ERIC Educational Resources Information Center

    Walker, Karen

    2006-01-01

    What are the benefits of a Fine Arts education? With the advent of the No Child Left Behind Act of 2000, extreme pressure has been put on schools to concentrate the majority of their efforts and resources on reading, math and science skills. Yet, NCLB also states that every child should be well-versed in the arts. Some research has shown that when…

  3. Chemicals from Cradle to Grave

    ERIC Educational Resources Information Center

    Science Scope, 2005

    2005-01-01

    About two years ago, an urban school district had planned for the disposal of some hazardous chemicals. It contracted with a chemical recycling company that was considered to be reputable. The school district, along with several other companies, was charged and fined by the Environmental Protection Agency for improperly releasing hazardous…

  4. Chemicals from Cradle to Grave

    ERIC Educational Resources Information Center

    Science Scope, 2005

    2005-01-01

    About two years ago, an urban school district had planned for the disposal of some hazardous chemicals. It contracted with a chemical recycling company that was considered to be reputable. The school district, along with several other companies, was charged and fined by the Environmental Protection Agency for improperly releasing hazardous…

  5. Analysis of Cadmium in Undissolved Anode Materials of Mark-IV Electrorefiner

    SciTech Connect

    Tae-Sic Yoo; Guy L. Fredrickson; DeeEarl Vaden; Brian R. Westphal

    2013-10-01

    The Mark-IV electrorefiner (Mk-IV ER) contains an electrolyte/molten cadmium system for refining uranium electrochemically. Typically, the anode of the Mk-IV ER consists of the chopped sodium-bonded metallic driver fuels, which have been primarily U-10Zr binary fuels. Chemical analysis of the residual anode materials after electrorefining indicates that a small amount of cadmium is removed from the Mk-IV ER along with the undissolved anode materials. Investigation of chemical analysis data indicates that the amount of cadmium in the undissolved anode materials is strongly correlated with the anode rotation speeds and the residence time of the anode in the Mk-IV ER. Discussions are given to explain the prescribed correlation.

  6. Study of fine sediments for making lightweight aggregate.

    PubMed

    Hung, Meng-Feng; Hwang, Chao-Lung

    2007-10-01

    The objective of this study was to investigate the recycling of the fine sediments of Shih-Men Reservoir to manufacture lightweight aggregate. By qualitative and quantitative analysis of the fine sediment and sintered aggregate through soil test, X-ray fluorescence, X-ray diffraction and scanning electron microscopy, a strategy of recycling fine sediment as aggregate for other similar material is proposed. The test results indicate that such fine sediment can be classified as low plastic clay, and clay of such chemical composition is located in the Riley's 'area of bloating'. The particle density of sintered lightweight aggregate decreases when the sintering temperature increases especially above 1200 degrees C due to phase transformation and formation of a vitrified layer on the surface through subsequent dehydration, bloating and collapsing stages. Our findings show that the fine sediment of Shin-Men Reservoir could be a suitable raw material for making expanded lightweight aggregate sintered at 1200 to 1300 degrees C for 10 to 12 min by a programmable furnace and a diffusion process.

  7. Facile Routes to Th(IV), U(IV), and Np(IV) Phosphites and Phosphates

    SciTech Connect

    Villa, Eric M.; Wang, Shuao; Alekseev, Evgeny V.; Depmeier, Wulf; Albrecht-Schmitt, Thomas E.

    2011-08-05

    Three actinide(IV) phosphites and a NpIV phosphate, AnIV(HPO₃)₂(H₂O)₂ (An = Th, U, Np) and Cs[Np(H1.5PO₄)(PO₄)]₂, respectively, were synthesized using mild hydrothermal conditions. The first three phases are isotypic and were obtained using similar reaction conditions. Cs[Np(H1.5PO₄)(PO₄)]₂ was synthesized using an analogous method to that of Np(HPO₃)₂(H₂O)₂. However, this fourth phase is quite different in comparison to the other phases in both composition and structure. The structure of Cs[Np(H1.5PO₄)(PO₄)]₂ is constructed from double layers of neptunium(IV) phosphate with caesium cations in the interlayer region. In contrast, An(HPO₃)₂(H₂O)₂ (An = Th, U, Np) form dense 3D networks. The actinide contraction is detected in variety of metrics obtained from single-crystal X-ray diffraction data. Changes in the oxidation state of the neptunium starting materials yield different products.

  8. Digestive Ripening: A Fine Chemical Machining Process on the Nanoscale.

    PubMed

    Shimpi, Jayesh R; Sidhaye, Deepti S; Prasad, Bhagavatula L V

    2017-09-26

    A comprehensive overview of the process of digestive ripening that is known to convert polydisperse nanocrystals to monodisperse ones is presented. Apart from highlighting the role of organic molecules (ligands) in achieving size control, the roles of other parameters such as the nanocrystal-ligand binding strength and the temperature at which the reaction is carried out in accomplishing size control are also delineated. The generality of the procedure is illustrated by providing examples of how it is used to prepare monodisperse nanocrystals of different metals, alloy systems, and ultrasmall nanocrystals and also to narrow the size distribution in complex binary and ternary nanocrystal systems. Finally, the current status as far as the theoretical understanding of how size control is being achieved by digestive ripening is laid out, emphasizing at the same time the necessity to undertake more systematic studies to completely realize the full potential of this practically very useful procedure.

  9. Recent Applications of Alkene Metathesis in Fine Chemical Synthesis

    NASA Astrophysics Data System (ADS)

    Bicchielli, Dario; Borguet, Yannick; Delaude, Lionel; Demonceau, Albert; Dragutan, Ileana; Dragutan, Valerian; Jossifov, Christo; Kalinova, Radostina; Nicks, François; Sauvage, Xavier

    During the last decade or so, the emergence of the metathesis reaction in organic synthesis has revolutionised the strategies used for the construction of complex molecular structures. Olefin metathesis is indeed particularly suited for the construction of small open-chain molecules and macrocycles using crossmetathesis and ring-closing metathesis, respectively. These reactions serve, inter alia, as key steps in the synthesis of various agrochemicals and pharmaceuticals such as macrocyclic peptides, cyclic sulfonamides, novel macrolides, or insect pheromones. The present chapter is aiming at illustrating the great synthetic potential of metathesis reactions. Shortcomings, such as the control of olefin geometry and the unpredictable effect of substituents on the reacting olefins, will also be addressed. Examples to be presented include epothilones, amphidinolides, spirofungin A, and archazolid. Synthetic approaches involving silicon-tethered ring-closing metathesis, relay ring-closing metathesis, sequential reactions, domino as well as tandem metathesis reactions will also be illustrated.

  10. Toward Phase IV, Populating the WOVOdat Database

    NASA Astrophysics Data System (ADS)

    Ratdomopurbo, A.; Newhall, C. G.; Schwandner, F. M.; Selva, J.; Ueda, H.

    2009-12-01

    One of challenges for volcanologists is the fact that more and more people are likely to live on volcanic slopes. Information about volcanic activity during unrest should be accurate and rapidly distributed. As unrest may lead to eruption, evacuation may be necessary to minimize damage and casualties. The decision to evacuate people is usually based on the interpretation of monitoring data. Over the past several decades, monitoring volcanoes has used more and more sophisticated instruments. A huge volume of data is collected in order to understand the state of activity and behaviour of a volcano. WOVOdat, The World Organization of Volcano Observatories (WOVO) Database of Volcanic Unrest, will provide context within which scientists can interpret the state of their own volcano, during and between crises. After a decision during the 2000 IAVCEI General Assembly to create WOVOdat, development has passed through several phases, from Concept Development (Phase-I in 2000-2002), Database Design (Phase-II, 2003-2006) and Pilot Testing (Phase-III in 2007-2008). For WOVOdat to be operational, there are still two (2) steps to complete, which are: Database Population (Phase-IV) and Enhancement and Maintenance (Phase-V). Since January 2009, the WOVOdat project is hosted by Earth Observatory of Singapore for at least a 5-year period. According to the original planning in 2002, this 5-year period will be used for completing the Phase-IV. As the WOVOdat design is not yet tested for all types of data, 2009 is still reserved for building the back-end relational database management system (RDBMS) of WOVOdat and testing it with more complex data. Fine-tuning of the WOVOdat’s RDBMS design is being done with each new upload of observatory data. The next and main phase of WOVOdat development will be data population, managing data transfer from multiple observatory formats to WOVOdat format. Data population will depend on two important things, the availability of SQL database in volcano

  11. Process for cleaning fine coal

    SciTech Connect

    Ennis, R.E.

    1981-08-04

    A process for the wet concentration and cleaning of fine coal is provided which comprises the steps of desliming and thickening a dilute slurry of fine coal and contaminant particles having a size of less than about 10 mm by introducing the same to a hydrocyclone separator to retain a slurry of particles having a size greater than about 0.1 mm, wet concentrating the last-named slurry and removing the heavier contaminant particles by introducing it to an autogenous dense medium separation vessel having a manifold for injecting water at an intermediate level and controlling the underflow of heavier than coal particles to maintain a fluidized bed of heavier particles and causing a slurry of the lighter coal particles to overflow, and concentrating and dewatering the overflow by means of a static or vibratory sizing screen.

  12. Wetter for fine dry powder

    DOEpatents

    Hall, James E.; Williams, Everett H.

    1977-01-01

    A system for wetting fine dry powders such as bentonite clay with water or other liquids is described. The system includes a wetting tank for receiving water and a continuous flow of fine powder feed. The wetting tank has a generally square horizontal cross section with a bottom end closure in the shape of an inverted pyramid. Positioned centrally within the wetting tank is a flow control cylinder which is supported from the walls of the wetting tank by means of radially extending inclined baffles. A variable speed motor drives a first larger propeller positioned immediately below the flow control cylinder in a direction which forces liquid filling the tank to flow downward through the flow control cylinder and a second smaller propeller positioned below the larger propeller having a reverse pitch to oppose the flow of liquid being driven downward by the larger propeller.

  13. Compressive behavior of fine sand.

    SciTech Connect

    Martin, Bradley E.; Kabir, Md. E.; Song, Bo; Chen, Wayne

    2010-04-01

    The compressive mechanical response of fine sand is experimentally investigated. The strain rate, initial density, stress state, and moisture level are systematically varied. A Kolsky bar was modified to obtain uniaxial and triaxial compressive response at high strain rates. A controlled loading pulse allows the specimen to acquire stress equilibrium and constant strain-rates. The results show that the compressive response of the fine sand is not sensitive to strain rate under the loading conditions in this study, but significantly dependent on the moisture content, initial density and lateral confinement. Partially saturated sand is more compliant than dry sand. Similar trends were reported in the quasi-static regime for experiments conducted at comparable specimen conditions. The sand becomes stiffer as initial density and/or confinement pressure increases. The sand particle size become smaller after hydrostatic pressure and further smaller after dynamic axial loading.

  14. SOUTHERN FINE PARTICULATE MONITORING PROJECT

    SciTech Connect

    Ashley D. Williamson

    2001-07-01

    This is the third quarterly progress report of the ''Southern Fine Particulate Monitoring Project'', funded by the U.S. Department of Energy's National Energy Technology Laboratory under DOE Cooperative Agreement No. DE-FC26-00NT40770 to Southern Research Institute (SRI). In this two year project SRI will conduct detailed studies of ambient fine particulate matter in the Birmingham, AL metropolitan area. Project objectives include: Augment existing measurements of primary and secondary aerosols at an established urban southeastern monitoring site; Make a detailed database of near-continuous measurements of the time variation of fine particulate mass, composition, and key properties (including particle size distribution); Apply the measurements to source attribution, time/transport properties of fine PM, and implications for management strategies for PM{sub 2.5}; and Validate and compare key measurement methods used in this study for applicability within other PM{sub 2.5} research by DOE-FE, EPA, NARSTO, and others. During the third project quarter, the new SRI air monitoring shelter and additional instruments were installed at the site. Details include: Installation of Radiance Research M903 Nephelometer; Installation of SRI air monitoring shelter at North Birmingham Site; Relocation of instruments from SEARCH shelter to SRI shelter; Installation of Rupprecht & Patashnick 8400 Sulfate Monitor; Assembly and initial laboratory testing for particulate sulfate monitor of Harvard design; Efficiency testing of particle sizing instrument package at SRI lab; Preparation for the Eastern Supersite July measurement intensive program; and Continued monitoring with TEOM and particle sizing instruments.

  15. The composition of fine fragrances is changing.

    PubMed

    Rastogi, Suresh C; Menné, Torkil; Johansen, Jeanne Duus

    2003-03-01

    High frequencies of contact allergy to fragrance ingredients have been reported in recent years. Developments in analytical chemistry have made it possible to measure exposure to well-known fragrance contact allergens. It has been shown that exposure is widespread in different types of products. The products with the highest concentrations of allergens have been shown to be prestige perfumes intended for women. This investigation explores the possible development in formulation of prestige perfumes, with regard to their content of the chemically defined ingredients of the diagnostic patch test material, the fragrance mix (FM). 10 fine fragrances were subjected to chemical analysis: 5 of these had been launched years ago (1921-1990) and 5 were the latest launches by the same companies, introduced 2 months to 4 years before purchase. The analysis revealed that the 5 old perfumes contained a mean of 5 of the 7 target allergens of the FM, while the new perfumes contained a mean of 2.8 of the allergens. The mean concentrations of the target allergens were 2.6 times higher in the old perfumes than in the new perfumes, range 2.2-337. It is concluded that the old perfumes, which are still popular products on the market, have a different composition from the new perfumes. This may be due to change in fashion or to an effort by the fragrance industry to focus on fragrance contact allergy, especially that to the FM ingredients.

  16. Anaerobic digestion of fines from recovered paper processing - Influence of fiber source, lignin and ash content on biogas potential.

    PubMed

    Steffen, Friedrich; Requejo, Ana; Ewald, Christian; Janzon, Ron; Saake, Bodo

    2016-01-01

    Fines concentration harms paper machine runability and output quality in recovered paper processing, hence, their extraction would be fundamentally beneficial. In this study, separated fines from an industrial recycled fiber pulp (RFP) were characterized and evaluated for their potential biogas yields with a focus on understanding the role of varying lignin and ash contents. Further, these results were compared with biogas yields from conventional chemical and mechanical pulps. Overall, methane yields of fines from mechanical pulps (21-28mL/gVS) and RFP (127mL/gVS) are relatively low compared to the high methane yields of 375mL/gVS from the chemical pulp fines. However, it was shown that the high ash content in RFP fines (up to 50%) did not negatively influence overall yield, rather, it was the presence of slowly biodegrading lignin-rich fiber fines.

  17. Genetics Home Reference: mucopolysaccharidosis type IV

    MedlinePlus

    ... types of mucopolysaccharidosis, MPS IV does not affect intelligence. The life expectancy of individuals with MPS IV ... qualified healthcare professional . About Selection Criteria for Links Data Files & API Site Map Customer Support USA.gov ...

  18. SPECIATION OF GAS-PHASE AND FINE PARTICLE EMISSIONS FROM BURNING OF FOLIAR FUELS

    EPA Science Inventory

    Particle size distributions (10-1000 nm aerodynamic diameter), physical and chemical properties of fine particle matter (PM2.5) with aerodynamic diameter <2.5 micrometers, and gas-phase emissions from controlled open burning of assorted taxa were measured. Chemical speciation of ...

  19. SPECIATION OF GAS-PHASE AND FINE PARTICLE EMISSIONS FROM BURNING OF FOLIAR FUELS

    EPA Science Inventory

    Particle size distributions (10-1000 nm aerodynamic diameter), physical and chemical properties of fine particle matter (PM2.5) with aerodynamic diameter <2.5 micrometers, and gas-phase emissions from controlled open burning of assorted taxa were measured. Chemical speciation of ...

  20. 36 CFR 910.35 - Fine arts.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 36 Parks, Forests, and Public Property 3 2013-07-01 2012-07-01 true Fine arts. 910.35 Section 910... DEVELOPMENT AREA Standards Uniformly Applicable to the Development Area § 910.35 Fine arts. Fine arts... of art which are appropriate for the development. For information and guidance, a...

  1. 36 CFR 910.35 - Fine arts.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 36 Parks, Forests, and Public Property 3 2012-07-01 2012-07-01 false Fine arts. 910.35 Section 910... DEVELOPMENT AREA Standards Uniformly Applicable to the Development Area § 910.35 Fine arts. Fine arts... of art which are appropriate for the development. For information and guidance, a...

  2. 36 CFR 910.35 - Fine arts.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 36 Parks, Forests, and Public Property 3 2014-07-01 2014-07-01 false Fine arts. 910.35 Section 910... DEVELOPMENT AREA Standards Uniformly Applicable to the Development Area § 910.35 Fine arts. Fine arts... of art which are appropriate for the development. For information and guidance, a...

  3. Considering Fine Art and Picture Books

    ERIC Educational Resources Information Center

    Serafini, Frank

    2015-01-01

    There has been a close association between picturebook illustrations and works of fine art since the picturebook was first conceived, and many ways these associations among works of fine art and picturebook illustrations and design play out. To make sense of all the various ways picturebook illustrations are associated with works of fine art,…

  4. Fine Mode Aerosol over the United Arab Emirates

    NASA Astrophysics Data System (ADS)

    Ross, K. E.; Piketh, S. J.; Reid, J. S.; Reid, E. A.

    2005-12-01

    The aerosol loading of the atmosphere over the Arabian Gulf region is extremely diverse and is composed not only of dust, but also of pollution that is derived largely from oil-related activities. Fine mode pollution particles are most efficient at scattering incoming solar radiation and have the potential to act as cloud condensation nuclei (CCN), and may therefore have implications for climate change. The smaller aerosols may also pose a health hazard if present in high concentrations. The United Arab Emirates Unified Aerosol Experiment (UAE2) was designed to investigate aerosol and meteorological characteristics over the region using ground-based, aircraft and satellite measurements, and was conducted in August and September 2004. Aerosol chemical composition has been obtained from filters that were collected at the site of the Mobile Atmospheric Aerosol and Radiation Characterization Observatory (MAARCO) on the coast of the UAE between Abu Dhabi and Dubai. Filter samples were also collected on an airborne platform in order to assess how aerosol chemical composition varies across the region and throughout the depth of the boundary layer. Results of the analysis of the PM2.5 coastal samples show that ammonium sulphate is the most prevalent constituent of the fine mode aerosol in the region (>50% of the mass), followed by organic matter, alumino-silicates, calcium carbonate and black carbon. Source apportionment indicates that most of the fine aerosol mass is derived from fossil fuel combustion, while mineral dust and local vehicle emissions also contribute to the fine aerosol loading. The organic carbon-to-total carbon ratio of the aerosol is 0.65, which is typical of fossil fuel combustion. The dominance of sulphates means that the fine mode aerosol in the region is probably responsible for a negative radiative forcing, and that the polluting emissions significantly elevate the concentration of CCN.

  5. Luna 24 regolith breccias: A possible source of the fine size material of the Luna 24 regolith

    NASA Technical Reports Server (NTRS)

    Rode, O. D.; Lindstrom, M. M.

    1994-01-01

    The regolith breccias from the Luna 24 core were analyzed. The Luna 24 regolith is a mixture of fine and coarse grain materials. The comparable analysis of the grain size distributions, the modal and chemical compositions of the breccias, and the regolith from the same levels show that the friable slightly litificated breccia with a friable fine grain matrix may be a source of fine grain material of the Luna 24 present day regolith.

  6. Geochemistry of Fine-grained Sediments and Sedimentary Rocks

    NASA Astrophysics Data System (ADS)

    Sageman, B. B.; Lyons, T. W.

    2003-12-01

    The nature of detrital sedimentary (siliciclastic) rocks is determined by geological processes that occur in the four main Earth surface environments encountered over the sediment's history from source to final sink: (i) the site of sediment production (provenance), where interactions among bedrock geology, tectonic uplift, and climate control weathering and erosion processes; (ii) the transport path, where the medium of transport, gradient, and distance to the depositional basin may modify the texture and composition of weathered material; (iii) the site of deposition, where a suite of physical, chemical, and biological processes control the nature of sediment accumulation and early burial modification; and (iv) the conditions of later burial, where diagenetic processes may further alter the texture and composition of buried sediments. Many of these geological processes leave characteristic geochemical signatures, making detrital sedimentary rocks one of the most important archives of geochemical data available for reconstructions of ancient Earth surface environments. Although documentation of geochemical data has long been a part of the study of sedimentation (e.g., Twenhofel, 1926, 1950; Pettijohn, 1949; Trask, 1955), the development and application of geochemical methods specific to sedimentary geological problems blossomed in the period following the Second World War ( Degens, 1965; Garrels and Mackenzie, 1971) and culminated in recent years, as reflected by the publication of various texts on marine geochemistry (e.g., Chester, 1990, 2000), biogeochemistry (e.g., Schlesinger, 1991; Libes, 1992), and organic geochemistry (e.g., Tissot and Welte, 1984; Engel and Macko, 1993).Coincident with the growth of these subdisciplines a new focus has emerged in the geological sciences broadly represented under the title of "Earth System Science" (e.g., Kump et al., 1999). Geochemistry has played the central role in this revolution (e.g., Berner, 1980; Garrels and Lerman

  7. Stage IV-S neuroblastoma. Results with definitive therapy

    SciTech Connect

    Stokes, S.H.; Thomas, P.R.; Perez, C.A.; Vietti, T.J.

    1984-05-15

    The results of management of 14 patients with Stage IV-S neuroblastoma are reported. The treatment policy, although not consistent over this time span, in general used a combination of radiotherapy and chemotherapy or infrequently one modality alone. Twelve of 14 (86%) survived more than 6 years. One patient, with a solitary mediastinal primary tumor, died of rapidly progressive disease at three months. The other death occurred in a 4.5-year-old presenting with hepatomegaly at diagnosis followed by skeletal dissemination 2.5 years later. Thirteen of the patients were younger than 1 year of age. Of the 11 patients that received radiotherapy, 4 experienced mild asymptomatic scoliosis or kyphoscoliosis at 3 to 12 years after initial therapy. A review of the literature indicates that spontaneous regression in this tumor is very frequent; therefore, it is recommended that for the common presentation of massive hepatomegaly in an infant, close observation is warranted, unless life threatening complications occur. However, initial therapeutic intervention may be indicated in those patients with life threatening presentations. This data did not substantiate the necessity for complete surgical excision of the primary tumor, as has been suggested by others.

  8. Oxovanadium(IV) silsesquioxane complexes.

    PubMed

    Ohde, Christian; Limberg, Christian; Stösser, Reinhard; Demeshko, Serhiy

    2010-03-01

    In the context of a potential modeling of reduced oxovanadium species occurring on the surfaces of silica-supported vanadia catalysts in the course of its turnover, the incompletely condensed silsesquioxane H(3)(c-pentyl)T(7) was reacted with Cl(4)V(THF)(2) (where THF = tetrahydrofuran) in the presence of triethylamine. Precipitation of 3 equiv of HNEt(3)Cl seemed to point to the clean formation of [((c-pentyl)T(7))(V(IV)Cl)] (1), which was supported by electron paramagnetic resonance studies performed for the resulting solutions, but further analytical and spectroscopic investigations showed that the processes occurring at that stage are more complex than that and even include the formation of [((c-pentyl)T(7))(V(V)O)](2) as a side product. Storage of a red-brown hexane solution of this product mixture reproducibly led to the precipitation of blue crystals belonging to the chloride-free compound [((c-pentyl)T(7))(2)(V(IV)=O)(3)(THF)(2)] (2), as revealed by single-crystal X-ray diffraction. Performing the same reaction in the presence of 2 equiv of pyridine leads to an analogous product, where the THF ligands are replaced by pyridine. Subsequent investigations showed that the terminal oxo ligands at the vanadium centers are, on the one hand, due to the presence of adventitious water; on the other hand, the [(c-pentyl)T(7)](3-) ligand also acted as a source of O(2-). The results of SQUID measurements performed for 2 can be interpreted in terms of a ferromagnetic coupling between the vanadyl units. Exposing 2 to a dioxygen atmosphere resulted in its immediate oxidation to yield the V(V) complex [((c-pentyl)T(7))(V(V)O)](2), which may model a fast reoxidation reaction of oxovanadium(IV) trimers on silica surfaces.

  9. PREPARATION OF OXOPORPHINATOMANGANESE (IV) COMPLEX

    SciTech Connect

    Willner, I.; Otvos, J.; Calvin, M.

    1980-07-01

    Oxo-manganese-tetraphenylporphyrin (O=Mn{sup IV}-TPP) has been prepared by an oxygen-transfer reaction from iodosylbenzene to MnIITPP and characterized by its i.r. and field desorption mass spectra, which are identical to those of the product obtained by direct oxidation of Mn{sup III}(TPP) in an aqueous medium; it transfers oxygen to triphenylphosphine to produce triphenylphosphine oxide, and it is suggested that similar intermediates are important in oxygen activation by cytochrome P-450 as well as in the photosynthetic evolution of oxygen.

  10. Method for cleaning fine coal

    SciTech Connect

    Smit, F.J.

    1985-07-16

    A method for cleaning fine coal is provided which includes: mixing the coal with a fluid of such a specific gravity that clean coal particles would float while refuse particles would sink therein, pretreating the coalfluid slurry by adding a surfactant, subjecting the mixture to ultrasonic dispersion, and separating the entire mixture into higher and lower specific gravity fluid streams by means of centrifugal separation. The fluid of the chosen specific gravity and the surfactant may be recovered from the fluid streams and recycled if desired.

  11. Test Review: Advanced Clinical Solutions for WAIS-IV and WMS-IV

    ERIC Educational Resources Information Center

    Chu, Yiting; Lai, Mark H. C.; Xu, Yining; Zhou, Yuanyuan

    2012-01-01

    The authors review the "Advanced Clinical Solutions for WAIS-IV and WMS-IV". The "Advanced Clinical Solutions (ACS) for the Wechsler Adult Intelligence Scale-Fourth Edition" (WAIS-IV; Wechsler, 2008) and the "Wechsler Memory Scale-Fourth Edition" (WMS-IV; Wechsler, 2009) was published by Pearson in 2009. It is a…

  12. Test Review: Advanced Clinical Solutions for WAIS-IV and WMS-IV

    ERIC Educational Resources Information Center

    Chu, Yiting; Lai, Mark H. C.; Xu, Yining; Zhou, Yuanyuan

    2012-01-01

    The authors review the "Advanced Clinical Solutions for WAIS-IV and WMS-IV". The "Advanced Clinical Solutions (ACS) for the Wechsler Adult Intelligence Scale-Fourth Edition" (WAIS-IV; Wechsler, 2008) and the "Wechsler Memory Scale-Fourth Edition" (WMS-IV; Wechsler, 2009) was published by Pearson in 2009. It is a…

  13. Behavior of redox-sensitive elements during weathering of granite in subtropical area using X-ray absorption fine structure spectroscopy

    NASA Astrophysics Data System (ADS)

    Zhang, Zhuo-Jun; Liu, Cong-Qiang; Zhao, Zhi-Qi; Cui, Li-Feng; Liu, Wen-Jing; Liu, Tao-Ze; Liu, Bao-Jian; Fan, Bai-Ling

    2015-06-01

    The variation in chemical compositions of regolith along a weathering profile developed on a granite substrate in Jiangxi province, in southern China, was investigated in this paper, with the aim to characterize the speciation of redox-sensitive elements and to evaluate their mobility and redistribution during chemical weathering. Mass balance calculations indicate titanium (Ti) is the most immobile element in this weathering profile. A new method, X-ray absorption fine structure (XAFS) spectroscopy, was used to determine the speciation of Fe and Mn along the profile. Fe K-edge X-ray absorption near edge structure (XANES) spectra show Fe in saprolith is stabilized mainly in the state of Fe(III), suggesting Fe is as immobile as conservative elements during granite weathering. Mn K-edge XANES spectra show Mn (III/IV) oxides are reduced to Mn(II) in surface soil, where soil organic matter (SOM) acts as an important reductant. Although Ce, Co and V were unable to be analysed by XAFS, their concentrations have significant correlations with that of Mn, indicating that the mobilization and redistribution of Ce, Co and V may also be governed by redox condition. All in all, the results suggest that redox process impacts significantly on the redistribution of Mn, Ce, Co and V along the profile. The successful application of XAFS in the study on migration of redox-sensitive elements during granite chemical weathering has provided valuable information for the understanding and evaluating the geochemical behavior of elements in the environment.

  14. Separation of nitrocellulose fines from wastewater with polymers

    SciTech Connect

    Park, J.K.; Shen, X.; Kim, B.J.; Kim, S.

    1996-12-31

    Nitrocellulose (NC) fines are discharged to wastewater streams during manufacturing. Laboratory-scale tests were conducted to evaluate the turbidity and total suspended solids reduction by coagulation/flocculation/sedimentation, to determine the settling characteristics of flocculated NC fines, and to evaluate thickening and dewatering characteristics of settled flocculated NC fine sludge. Cationic polymers were very effective in treating the negatively charged NC-manufacturing wastewater. Under an optimum flocculation condition, the supernatant turbidity of below 1 mg/L was obtained. High turbidity removal was achieved at a wide dosage range of 0.2 to 1.0 mg/L. Optimum flocculation was found to occur at low doses of the polymers tested and the polymer with a higher charge density performed better. High molecular weight polymers produced large flocs which had a high floc settling rate. Therefore, a high charge density and molecular weight polymers are preferred to separate NC fines from wastewater streams. Turbidity removal was improved with increasing Gt values and tapered flocculation. High velocity gradient facilitated adequate dispersion of a polymer. On the other hand, long rapid mixing would cause some floc breakup. Significant improvement of dewatering characteristics of NC-manufacturing wastewater sludge was found to be facilitated by the residual effects of the polymers having undergone flocculation of the wastewater. It appears that further chemical conditioning of the sludge is not necessary.

  15. Synthesis and characterization of II-IV-V(2) semiconductors

    NASA Astrophysics Data System (ADS)

    Wen, Yuan-Chung

    1998-11-01

    The II-IV-V2 chalcopyrite semiconductors are isostructural and isoelectronic analogues of the III-V semiconductors. Like the III-V materials the compounds have potential applications in nonlinear optics, optoelectronics and solar energy conversion. The naturally abundant elements and high absorption coefficients in many of the II-IV-V2's make these materials more attractive for large scale applications. Our study focused on the investigation of the basic electrical and optical properties of a number of II-IV- V2 materials by photoelectrochemical methods and photoluminescence. A variety of single crystals in II-IV- V2 family such as ZnSiAs2, CdSiAs2, CdSiP2, ZnSiP2, CdGeP2, ZnGeP2, and ZnSnP2 have been synthesized by chemical vapor transport (CVT) and Bridgman growth techniques. Intentional doping with S, Se, Al, Ga and In of the crystals resulted in complex behavior. In some systems compensation with intrinsic acceptors was observed and in other systems the change of doping type and controllable doping levels were observed. The bandgap, doping level, band position, quantum yield and current voltage behavior in various electrolytes for many of the II-IV-V2 semiconductors have been determined using photoelectrochemical methods. Hall effect measurements of doping density have been used to compare with values obtained from Mott-Schottky analysis. Frequency and pH dependence of the Mott-Schottky plots were observed. The minority diffusion length of II-IV-V2 calculated from quantum yield and absorption coefficient data at the onset of photocurrent matches well to the prediction from the Gartner Model. Polarization dependent photoluminescence has been used for the study of interband transitions and optical anisotropy in CdSiAs2 and CdSiP2 crystals. The electrode surfaces of CdSiAs2 crystals treated by wet chemical etchants were investigated and characterized by XPS. 31P solid state MAS NMR studies of the II-IV- P2 compounds gave very sharp 31P resonances and revealed

  16. Southern Fine Particulate Monitoring Project

    SciTech Connect

    Ashley Williamson

    2003-05-31

    This final project report presents experimental details, results and analysis of continuous onsite ambient fine particulate data at the North Birmingham sampling site during the October, 2001-September, 2002 study period.The host site for these measurement activities is the North Birmingham PM monitoring station by the Jefferson County Health Department in Birmingham, AL.The continuous data include PM{sub 2.5} mass concentrations measured by TEOM, particle sulfate using the R&P 8400S monitor, particle size distributions measured by SMPS and APS monitors, and PM{sub 2.5} light scattering extinction coefficient as measured by nephelometer. During the course of the project, measurement intercomparison data were developed for these instruments and several complementary measurements at the site. The report details the instrument set and operating procedures and describes the resulting data. Report subsections present an overview summary of the data, followed by detailed description of the systematic time behavior of PM{sub 2.5} and other specific particulate size fractions. Specific subsections are included for particle size distribution, light scattering, and particle sulfate data. The final subsection addresses application of the measurements to the practical questions of fine PM generation and transport, source attribution, and PM{sub 2.5} management strategies.

  17. Magnetization of nano-fine particles of Pd/Ni alloys

    NASA Astrophysics Data System (ADS)

    Nunomura, N.; Teranishi, T.; Miyake, M.; Oki, A.; Yamada, S.; Toshima, N.; Hori, H.

    1998-01-01

    In order to investigate the giant magnetic moment problem in nano-fine Pd alloys particles, enough amount of Pd/Ni fine particles with quite narrow diameter distribution have been prepared by chemical method. The magnetization of Pd/Ni alloy ultrafine particles has been systematically investigated by using a SQUID magnetometer. The magnetization remarkably increases above the concentration of 8% of Ni. This result indicates the giant moment in the ultrafine Pd/Ni alloy particles.

  18. Cells that emerge from embryonic explants produce fibers of type IV collagen

    PubMed Central

    1985-01-01

    Double immunofluorescence staining experiments designed to examine the synthesis and deposition of collagen types I and IV in cultured explants of embryonic mouse lung revealed the presence of connective tissue-like fibers that were immunoreactive with anti-type IV collagen antibodies. This observation is contrary to the widely accepted belief that type IV collagen is found only in sheet-like arrangements beneath epithelia or as a sheath-like layer enveloping bundles of nerve or muscle cells. The extracellular matrix produced by cells that migrate from embryonic mouse lung rudiments in vitro was examined by double indirect immunofluorescence microscopy. Affinity-purified monospecific polyclonal antibodies were used to examine cells after growth on glass or native collagen substrata. The data show that embryonic mesenchymal cells can produce organized fibers of type IV collagen that are not contained within a basement membrane, and that embryonic epithelial cells deposit fibers and strands of type IV collagen beneath their basal surface when grown on glass; however, when grown on a rat tail collagen substratum the epithelial cells produce a fine meshwork. To our knowledge this work represents the first report that type IV collagen can be organized by cells into a fibrous extracellular matrix that is not a basement membrane. PMID:3900085

  19. IVS contribution to ITRF2014

    NASA Astrophysics Data System (ADS)

    Bachmann, Sabine; Thaller, Daniela; Roggenbuck, Ole; Lösler, Michael; Messerschmitt, Linda

    2016-07-01

    Every few years the International Terrestrial Reference System (ITRS) Center of the International Earth Rotation and Reference Systems Service (IERS) decides to generate a new version of the International Terrestrial Reference Frame (ITRF). For the upcoming ITRF2014 the official contribution of the International VLBI Service for Geodesy and Astrometry (IVS) comprises 5796 combined sessions in SINEX file format from 1979.6 to 2015.0 containing 158 stations, overall. Nine AC contributions were included in the combination process, using five different software packages. Station coordinate time series of the combined solution show an overall repeatability of 3.3 mm for the north, 4.3 mm for the east and 7.5 mm for the height component over all stations. The minimum repeatabilities are 1.5 mm for north, 2.1 mm for east and 2.9 mm for height. One of the important differences between the IVS contribution to the ITRF2014 and the routine IVS combination is the omission of the correction for non-tidal atmospheric pressure loading (NTAL). Comparisons between the amplitudes of the annual signals derived by the VLBI observations and the annual signals from an NTAL model show that for some stations, NTAL has a high impact on station height variation. For other stations, the effect of NTAL is low. Occasionally other loading effects have a higher influence (e.g. continental water storage loading). External comparisons of the scale parameter between the VTRF2014 (a TRF based on combined VLBI solutions), DTRF2008 (DGFI-TUM realization of ITRS) and ITRF2008 revealed a significant difference in the scale. A scale difference of 0.11 ppb (i.e. 0.7 mm on the Earth's surface) has been detected between the VTRF2014 and the DTRF2008, and a scale difference of 0.44 ppb (i.e. 2.8 mm on the Earth's surface) between the VTRF2014 and ITRF2008. Internal comparisons between the EOP of the combined solution and the individual solutions from the AC contributions show a WRMS in X- and Y-Pole between

  20. Goodpasture antigen of the glomerular basement membrane: localization to noncollagenous regions of type IV collagen.

    PubMed Central

    Wieslander, J; Barr, J F; Butkowski, R J; Edwards, S J; Bygren, P; Heinegård, D; Hudson, B G

    1984-01-01

    The glomerular basement membrane antigen in Goodpasture syndrome is a collagenase-resistant molecule with a monomer molecular weight of about 26,000. Type IV collagen isolated from glomerular basement membrane contains collagenase-resistant sequences within its structure. Polyacrylamide gel electrophoresis, enzyme-linked immunosorbent assay, and chemical analysis were used to demonstrate that the collagenase-resistant sequences of type IV collagen contain Goodpasture antigen. Images PMID:6328527

  1. Spring in Inca City IV

    NASA Image and Video Library

    2014-11-13

    At certain times in spring, fans take on a gray or blue appearance. This is the time in Inca City when this phenomenon happens, as seen in this image acquired by NASA Mars Reconnaissance Orbiter. On the ridge at the top of the image fans have lengthened and now look more gray than the blotches on the araneiforms. At the bottom of the image they are distinctly blue in color. Two theories have been suggested: perhaps fine particles sink into the seasonal layer of ice so they no longer appear dark. Or, maybe the gas that is released from under the ice condenses and falls to the surface as a bright fresh layer of frost. It is quite likely that both of these theories are correct. http://photojournal.jpl.nasa.gov/catalog/PIA18895

  2. Fine-Tuning the Activity of Metal-Organic Framework-Supported Cobalt Catalysts for the Oxidative Dehydrogenation of Propane.

    PubMed

    Li, Zhanyong; Peters, Aaron W; Platero-Prats, Ana E; Liu, Jian; Kung, Chung-Wei; Noh, Hyunho; DeStefano, Matthew R; Schweitzer, Neil M; Chapman, Karena W; Hupp, Joseph T; Farha, Omar K

    2017-10-04

    Few-atom cobalt-oxide clusters, when dispersed on a Zr-based metal-organic framework (MOF) NU-1000, have been shown to be active for the oxidative dehydrogenation (ODH) of propane at low temperatures (< 230 °C), affording a selective and stable propene production catalyst. In our current work, a series of promoter ions with varying Lewis acidity, including Ni(II), Zn(II), Al(III), Ti(IV) and Mo(VI), are anchored as metal-oxide,hydroxide clusters to NU-1000 followed by Co(II) ion deposition, yielding a series of NU-1000-supported bimetallic-oxo,hydroxo,aqua clusters. Using difference envelope density (DED) analyses, the spatial locations of the promoter ions and catalytic cobalt ions are determined. For all samples the promoter ions are sited between pairs of Zr6 nodes along the MOF c axis whereas the location of the cobalt ions varies with the promoter ions. These NU-1000-supported bimetallic-oxide clusters are active for propane ODH after thermal activation under O2 to open a cobalt coordination site and to oxidize Co(II) to Co(III), as evidenced by operando X-ray absorption spectroscopy at the Co K-edge. In accord with the decreasing Lewis acidity of the promoter ion, catalytic activity increases in the order: Mo(VI)IV)fine-tune the structure-dependent activity of MOF-supported heterogeneous catalysts. Coupled with mechanistic studies-computational or experimental-this ability may translate into informed prediction of improved catalysts for propane ODH and other chemical reactions.

  3. Fine Collimator Grids Using Silicon Metering Structure

    NASA Technical Reports Server (NTRS)

    Eberhard, Carol

    1998-01-01

    The project Fine Collimator Grids Using Silicon Metering Structure was managed by Dr. Carol Eberhard of the Electromagnetic Systems & Technology Department (Space & Technology Division) of TRW who also wrote this final report. The KOH chemical etching of the silicon wafers was primarily done by Dr. Simon Prussin of the Electrical Engineering Department of UCLA at the laboratory on campus. Moshe Sergant of the Superconductor Electronics Technology Department (Electronics Systems & Technology Division) of TRW and Dr. Prussin were instrumental in developing the low temperature silicon etching processes. Moshe Sergant and George G. Pinneo of the Microelectronics Production Department (Electronics Systems & Technology Division) of TRW were instrumental in developing the processes for filling the slots etched in the silicon wafers with metal-filled materials. Their work was carried out in the laboratories at the Space Park facility. Moshe Sergant is also responsible for the impressive array of Scanning Electron Microscope images with which the various processes were monitored. Many others also contributed their time and expertise to the project. I wish to thank them all.

  4. Developing a biomonitoring tool for fine sediment

    NASA Astrophysics Data System (ADS)

    Turley, Matt; Bilotta, Gary; Brazier, Richard; Extence, Chris

    2014-05-01

    Sediment is an essential component of freshwater ecosystems; however anthropogenic activities can lead to elevated sediment delivery which can impact on the physical, chemical and biological characteristics of these ecosystems. Ultimately, this can result in a loss of ecosystem services worth more than 1.7 trillion per annum. As such it is important that sediment, which is one of the most commonly attributed causes of water quality impairment globally, is managed in order to minimise these impacts. The current EU environmental quality standard for sediment (monitored in the form of suspended solids) is 25 mg L-1 for all environments. It is widely recognised that this standard is unsuitable and not ecologically relevant. Furthermore, it requires a substantial resource investment to monitor sediment in this form as part of national and international water resource legislation. In recognition of this the development of sediment-specific biomonitoring tools is receiving increasing attention. The Proportion of Sediment-Sensitive Invertebrates (PSI) index is one such tool that is designed to indicate levels of fine sediment (

  5. Optical and Infrared Interferometry IV

    NASA Astrophysics Data System (ADS)

    Rajagopal, Jayadev K.; Creech-Eakman, Michelle J.; Malbet, Fabien

    2014-08-01

    Optical and IR Interferometry IV at the SPIE 2014 symposium in Montreal had a strong and vibrant program. After initial fears about budget cuts and travel-funding constraints, the Program Committee had to work hard to accommodate as many quality submissions as possible. Innovative, creative and visionary work ensured that the field has progressed well, despite the bleak funding climate felt in the US, Europe and elsewhere. Montreal proved an excellent venue for this, the largest of Interferometry conferences and the only one that brings together practitioners from the world over. Let us summarize a few highlights to convey a glimpse of the excitement that is detailed in the rest of these Proceedings.

  6. Rhenium(IV) sulfide nanotubes.

    PubMed

    Brorson, Michael; Hansen, Thomas W; Jacobsen, Claus J H

    2002-10-02

    Rhenium(IV) sulfide, ReS(2), has been prepared with nanotubular morphology by carbon nanotube templating. A multiwall carbon nanotube material was impregnated with solutions of NH(4)ReO(4) or ReCl(5), followed by drying and sulfidation with H(2)S at 1000 degrees C. The composite material synthesized was characterized by high-resolution transmission electron microscopy and X-ray powder diffraction. Like previously described MS(2) nanotube compounds, ReS(2) has a layered structure consisting of S-M-S layers. Re atoms in ordinary ReS(2) are octahedrally coordinated with S, and tetranuclear metal clusters are present as a consequence of metal-metal bonds.

  7. The Apollo 15 coarse fines (4-10 mm)

    NASA Technical Reports Server (NTRS)

    Ryder, Graham; Sherman, Sarah Bean

    1989-01-01

    A new catalog of the Apollo 15 coarse fines particles is presented. Powell's macroscopic descriptions, resulting from his 1972 particle by particle binocular examination of all of the Apollo 15 4 to 10 mm fines samples, are retained. His groupings are also retained, but petrographic, chemical, and other data from later analyses are incorporated into this catalog to better characterize individual particles and describe the groups. A large number of particles have no characterization beyond that done by Powell. Complete descriptions of the particles and all known references are provided. The catalog is intended for anyone interested in the rock types collected by Dave Scott and Jim Irwin in the Hadley-Appenine region, and particularly for researchers requiring sample allocations.

  8. Fine Structure in Solar Flares.

    PubMed

    Warren

    2000-06-20

    We present observations of several large two-ribbon flares observed with both the Transition Region and Coronal Explorer (TRACE) and the soft X-ray telescope on Yohkoh. The high spatial resolution TRACE observations show that solar flare plasma is generally not confined to a single loop or even a few isolated loops but to a multitude of fine coronal structures. These observations also suggest that the high-temperature flare plasma generally appears diffuse while the cooler ( less, similar2 MK) postflare plasma is looplike. We conjecture that the diffuse appearance of the high-temperature flare emission seen with TRACE is due to a combination of the emission measure structure of these flares and the instrumental temperature response and does not reflect fundamental differences in plasma morphology at the different temperatures.

  9. Fine structures at pore boundary

    NASA Astrophysics Data System (ADS)

    Bharti, L.; Quintero Noda, C.; Joshi, C.; Rakesh, S.; Pandya, A.

    2016-10-01

    We present high resolution observations of fine structures at pore boundaries. The inner part of granules towards umbra show dark striations which evolve into a filamentary structure with dark core and `Y' shape at the head of the filaments. These filaments migrate into the umbra similar to penumbral filaments. These filaments show higher temperature, lower magnetic field strength and more inclined field compared to the background umbra. The optical depth stratification of physical quantities suggests their similarity with penumbral filaments. However, line-of-sight velocity pattern is different from penumbral filaments where they show downflows in the deeper layers of the atmosphere while the higher layers show upflows. These observations show filamentation in a simple magnetic configuration.

  10. Curium analysis in plutonium uranium mixed oxide by x-ray fluorescence and absorption fine structure spectroscopy.

    PubMed

    Degueldre, C; Borca, C; Cozzo, C

    2013-10-15

    Plutonium uranium mixed oxide (MOX) fuels are being used in commercial nuclear reactors. The actinides in these fuels need to be analyzed after irradiation for assessing their behaviour with regards to their environment and the coolant. In this work the study of the local occurrence, speciation and next-neighbour environment of curium (Cm) in the (Pu,U)O2 lattice within an irradiated (60 MW d kg(-1) average burn-up) MOX sample was performed employing micro-x-ray fluorescence (µ-XRF) and micro-x-ray absorption fine structure (µ-XAFS) spectroscopy. The chemical bonds, valences and stoichiometry of Cm (≈ 0.7 wt% in the rim and ≈ 0.03 wt% in the centre) are determined from the experimental data gained for the irradiated fuel material examined in its centre and peripheral (rim) zones of the fuel. Curium occurrence is also reduced from the centre (hot) to the periphery (colder) because of the condensation of these volatile oxides. In the irradiated sample Cm builds up as Cm(3+) species (>90%) within a [CmO8](13-) or [CmO7](11-) coordination environment and no (<10%) Cm(IV) can be detected in the rim zone. Curium dioxide is reduced because of the redox buffering activity of the uranium dioxide matrix and of its thermodynamic instability.

  11. Climate, soil and plant functional types as drivers of global fine-root trait variation

    DOE PAGES

    Freschet, Grégoire T.; Valverde-Barrantes, Oscar J.; Tucker, Caroline M.; ...

    2017-03-08

    Ecosystem functioning relies heavily on below-ground processes, which are largely regulated by plant fine-roots and their functional traits. However, our knowledge of fine-root trait distribution relies to date on local- and regional-scale studies with limited numbers of species, growth forms and environmental variation. We compiled a world-wide fine-root trait dataset, featuring 1115 species from contrasting climatic areas, phylogeny and growth forms to test a series of hypotheses pertaining to the influence of plant functional types, soil and climate variables, and the degree of manipulation of plant growing conditions on species fine-root trait variation. Most particularly, we tested the competing hypothesesmore » that fine-root traits typical of faster return on investment would be most strongly associated with conditions of limiting versus favourable soil resource availability. We accounted for both data source and species phylogenetic relatedness. We demonstrate that: (i) Climate conditions promoting soil fertility relate negatively to fine-root traits favouring fast soil resource acquisition, with a particularly strong positive effect of temperature on fine-root diameter and negative effect on specific root length (SRL), and a negative effect of rainfall on root nitrogen concentration; (ii) Soil bulk density strongly influences species fine-root morphology, by favouring thicker, denser fine-roots; (iii) Fine-roots from herbaceous species are on average finer and have higher SRL than those of woody species, and N2-fixing capacity positively relates to root nitrogen; and (iv) Plants growing in pots have higher SRL than those grown in the field. Synthesis. This study reveals both the large variation in fine-root traits encountered globally and the relevance of several key plant functional types and soil and climate variables for explaining a substantial part of this variation. Climate, particularly temperature, and plant functional types were the two

  12. Redox Controls over the Stability of U(IV) in Floodplains of the Upper Colorado River Basin.

    PubMed

    Noël, Vincent; Boye, Kristin; Lezama Pacheco, Juan S; Bone, Sharon E; Janot, Noémie; Cardarelli, Emily; Williams, Kenneth H; Bargar, John R

    2017-10-03

    Aquifers in the Upper Colorado River Basin (UCRB) exhibit persistent uranium (U) groundwater contamination plumes originating from former ore processing operations. Previous observations at Rifle, Colorado, have shown that fine grained, sulfidic, organic-enriched sediments accumulate U in its reduced form, U(IV), which is less mobile than oxidized U(VI). These reduced sediment bodies can subsequently act as secondary sources, releasing U back to the aquifer. There is a need to understand if U(IV) accumulation in reduced sediments is a common process at contaminated sites basin-wide, to constrain accumulated U(IV) speciation, and to define the biogeochemical factors controlling its reactivity. We have investigated U(IV) accumulation in organic-enriched reduced sediments at three UCRB floodplains. Noncrystalline U(IV) is the dominant form of accumulated U, but crystalline U(IV) comprises up to ca. 30% of total U at some locations. Differing susceptibilities of these species to oxidative remobilization can explain this variability. Particle size, organic carbon content, and pore saturation, control the exposure of U(IV) to oxidants, moderating its oxidative release. Further, our data suggest that U(IV) can be mobilized under deeply reducing conditions, which may contribute to maintenance and seasonal variability of U in groundwater plumes in the UCRB.

  13. Extending the Use of Highly Porous and Functionalized MOFs to Th(IV) Capture.

    PubMed

    Zhang, Nan; Yuan, Li-Yong; Guo, Wen-Lu; Luo, Shi-Zhong; Chai, Zhi-Fang; Shi, Wei-Qun

    2017-08-02

    Thorium separation has recently become a hot topic because of the potential application of thorium as a future nuclear fuel, while metal-organic framework (MOF) materials have received much attention in the separation field due to their unique properties. Herein, a highly porous and stable MOF, UiO-66, and its carboxyl derivatives (UiO-66-COOH and UiO-66-(COOH)2) were synthesized and explored for the first time for Th(IV) capture from a weak acidic solution. Although the introduction of carboxyl groups into UiO-66 leads to an obvious decrease in the surface area and pore volume, the adsorbability toward Th(IV) is greatly enhanced. At pH = 3.0, the saturated sorption capacity for Th(IV) into UiO-66-(COOH)2 reached 350 mg/g, representing one of the largest values for Th(IV) capture by solid extraction. Moreover, the functionalized MOFs show fast sorption kinetics and desirable selectivity toward Th(IV) over a range of competing metal ions. A possible mechanism for the selective recognition of Th(IV) by these MOFs was explored on the basis of extended X-ray absorption fine structure and Fourier transform infrared analysis. It is concluded that UiO-66-COOH and UiO-66-(COOH)2 sorb Th(IV) through the coordination of carboxyl anions in the pores of the MOFs, whereas in the case of UiO-66, both the precipitation and the exchange with the organic solvent contribute to the Th(IV) uptake. This study contributes to the assessment of the feasibility of MOFs applied in actinides separation and better understanding of actinides sorption behavior in this kind of hybrid porous solid materials.

  14. Fine structures of type III radio bursts observed by LOFAR

    NASA Astrophysics Data System (ADS)

    Magdalenic, Jasmina; Marque, Christophe; Fallows, Richard; Mann, Gottfried; Vocks, Christian

    2017-04-01

    On August 25, 2014, NOAA AR 2146 produced the M2.0 class flare (peaked at 15:11 UT). The flare was associated with a coronal dimming, a EUV wave, a halo CME and a radio event observed by LOFAR (the LOw-Frequency Array). The radio event consisted of a type II, type III and type IV radio emissions. In this study, we focus on LOFAR observations of the type III bursts, generally considered to be radio signatures of fast electron beams propagating along open or quasi open field lines. The group of type III bursts was, as usually, observed during the impulsive phase of the flare. At first hand, type III bursts show no peculiarity, but the high frequency/time resolution LOFAR observations reveal that only few of these type III bursts have a smooth emission profile. The majority of bursts is strongly fragmented. Some show a structuring similar to type IIIb bursts, but on a smaller frequency scale, and others show a non-organized patchy structure which gives indication on the possibly related turbulence processes. Although fine structures of type III bursts were already reported, the wealth of fine structures, and the fragmentation of the radio emission observed in this August 25 event is unprecedented. We show that these LOFAR observations bring completely new insight and pose a new challenge for the physics of the acceleration of electron beams and associated emission processes.

  15. Modeling of Fine-Particle Formation in Turbulent Flames

    NASA Astrophysics Data System (ADS)

    Raman, Venkat; Fox, Rodney O.

    2016-01-01

    The generation of nanostructured particles in high-temperature flames is important both for the control of emissions from combustion devices and for the synthesis of high-value chemicals for a variety of applications. The physiochemical processes that lead to the production of fine particles in turbulent flames are highly sensitive to the flow physics and, in particular, the history of thermochemical compositions and turbulent features they encounter. Consequently, it is possible to change the characteristic size, structure, composition, and yield of the fine particles by altering the flow configuration. This review describes the complex multiscale interactions among turbulent fluid flow, gas-phase chemical reactions, and solid-phase particle evolution. The focus is on modeling the generation of soot particles, an unwanted pollutant from automobile and aircraft engines, as well as metal oxides, a class of high-value chemicals sought for specialized applications, including emissions control. Issues arising due to the numerical methods used to approximate the particle number density function, the modeling of turbulence-chemistry interactions, and model validation are also discussed.

  16. Advanced Fine Particulate Characterization Methods

    SciTech Connect

    Steven Benson; Lingbu Kong; Alexander Azenkeng; Jason Laumb; Robert Jensen; Edwin Olson; Jill MacKenzie; A.M. Rokanuzzaman

    2007-01-31

    The characterization and control of emissions from combustion sources are of significant importance in improving local and regional air quality. Such emissions include fine particulate matter, organic carbon compounds, and NO{sub x} and SO{sub 2} gases, along with mercury and other toxic metals. This project involved four activities including Further Development of Analytical Techniques for PM{sub 10} and PM{sub 2.5} Characterization and Source Apportionment and Management, Organic Carbonaceous Particulate and Metal Speciation for Source Apportionment Studies, Quantum Modeling, and High-Potassium Carbon Production with Biomass-Coal Blending. The key accomplishments included the development of improved automated methods to characterize the inorganic and organic components particulate matter. The methods involved the use of scanning electron microscopy and x-ray microanalysis for the inorganic fraction and a combination of extractive methods combined with near-edge x-ray absorption fine structure to characterize the organic fraction. These methods have direction application for source apportionment studies of PM because they provide detailed inorganic analysis along with total organic and elemental carbon (OC/EC) quantification. Quantum modeling using density functional theory (DFT) calculations was used to further elucidate a recently developed mechanistic model for mercury speciation in coal combustion systems and interactions on activated carbon. Reaction energies, enthalpies, free energies and binding energies of Hg species to the prototype molecules were derived from the data obtained in these calculations. Bimolecular rate constants for the various elementary steps in the mechanism have been estimated using the hard-sphere collision theory approximation, and the results seem to indicate that extremely fast kinetics could be involved in these surface reactions. Activated carbon was produced from a blend of lignite coal from the Center Mine in North Dakota and

  17. Level IV Ecoregions of Nevada

    EPA Pesticide Factsheets

    Ecoregions by state were extracted from the seamless national shapefile. Ecoregions denote areas of general similarity in ecosystems and in the type, quality, and quantity of environmental resources. They are designed to serve as a spatial framework for the research, assessment, management, and monitoring of ecosystems and ecosystem components. These general purpose regions are critical for structuring and implementing ecosystem management strategies across federal agencies, state agencies, and nongovernment organizations that are responsible for different types of resources within the same geographical areas. The approach used to compile this map is based on the premise that ecological regions can be identified through the analysis of patterns of biotic and abiotic phenomena, including geology, physiography, vegetation, climate, soils, land use, wildlife, and hydrology. The relative importance of each characteristic varies from one ecological region to another. A Roman numeral hierarchical scheme has been adopted for different levels for ecological regions. Level I is the coarsest level, dividing North America into 15 ecological regions. Level II divides the continent into 50 regions (Commission for Environmental Cooperation Working Group, 1997). At Level III, the continental United States contains 105 regions whereas the conterminous United States has 85 (U.S. Environmental Protection Agency, 2011). Level IV ecoregions are further subdivisions of Level III eco

  18. Level IV Ecoregions of Wyoming

    EPA Pesticide Factsheets

    Ecoregions by state were extracted from the seamless national shapefile. Ecoregions denote areas of general similarity in ecosystems and in the type, quality, and quantity of environmental resources. They are designed to serve as a spatial framework for the research, assessment, management, and monitoring of ecosystems and ecosystem components. These general purpose regions are critical for structuring and implementing ecosystem management strategies across federal agencies, state agencies, and nongovernment organizations that are responsible for different types of resources within the same geographical areas. The approach used to compile this map is based on the premise that ecological regions can be identified through the analysis of patterns of biotic and abiotic phenomena, including geology, physiography, vegetation, climate, soils, land use, wildlife, and hydrology. The relative importance of each characteristic varies from one ecological region to another. A Roman numeral hierarchical scheme has been adopted for different levels for ecological regions. Level I is the coarsest level, dividing North America into 15 ecological regions. Level II divides the continent into 50 regions (Commission for Environmental Cooperation Working Group, 1997). At Level III, the continental United States contains 105 regions whereas the conterminous United States has 85 (U.S. Environmental Protection Agency, 2011). Level IV ecoregions are further subdivisions of Level III eco

  19. Level IV Ecoregions of California

    EPA Pesticide Factsheets

    Ecoregions by state were extracted from the seamless national shapefile. Ecoregions denote areas of general similarity in ecosystems and in the type, quality, and quantity of environmental resources. They are designed to serve as a spatial framework for the research, assessment, management, and monitoring of ecosystems and ecosystem components. These general purpose regions are critical for structuring and implementing ecosystem management strategies across federal agencies, state agencies, and nongovernment organizations that are responsible for different types of resources within the same geographical areas. The approach used to compile this map is based on the premise that ecological regions can be identified through the analysis of patterns of biotic and abiotic phenomena, including geology, physiography, vegetation, climate, soils, land use, wildlife, and hydrology. The relative importance of each characteristic varies from one ecological region to another. A Roman numeral hierarchical scheme has been adopted for different levels for ecological regions. Level I is the coarsest level, dividing North America into 15 ecological regions. Level II divides the continent into 50 regions (Commission for Environmental Cooperation Working Group, 1997). At Level III, the continental United States contains 105 regions whereas the conterminous United States has 85 (U.S. Environmental Protection Agency, 2011). Level IV ecoregions are further subdivisions of Level III eco

  20. Level IV Ecoregions of Georgia

    EPA Pesticide Factsheets

    Ecoregions by state were extracted from the seamless national shapefile. Ecoregions denote areas of general similarity in ecosystems and in the type, quality, and quantity of environmental resources. They are designed to serve as a spatial framework for the research, assessment, management, and monitoring of ecosystems and ecosystem components. These general purpose regions are critical for structuring and implementing ecosystem management strategies across federal agencies, state agencies, and nongovernment organizations that are responsible for different types of resources within the same geographical areas. The approach used to compile this map is based on the premise that ecological regions can be identified through the analysis of patterns of biotic and abiotic phenomena, including geology, physiography, vegetation, climate, soils, land use, wildlife, and hydrology. The relative importance of each characteristic varies from one ecological region to another. A Roman numeral hierarchical scheme has been adopted for different levels for ecological regions. Level I is the coarsest level, dividing North America into 15 ecological regions. Level II divides the continent into 50 regions (Commission for Environmental Cooperation Working Group, 1997). At Level III, the continental United States contains 105 regions whereas the conterminous United States has 85 (U.S. Environmental Protection Agency, 2011). Level IV ecoregions are further subdivisions of Level III eco

  1. Level IV Ecoregions of Louisiana

    EPA Pesticide Factsheets

    Ecoregions by state were extracted from the seamless national shapefile. Ecoregions denote areas of general similarity in ecosystems and in the type, quality, and quantity of environmental resources. They are designed to serve as a spatial framework for the research, assessment, management, and monitoring of ecosystems and ecosystem components. These general purpose regions are critical for structuring and implementing ecosystem management strategies across federal agencies, state agencies, and nongovernment organizations that are responsible for different types of resources within the same geographical areas. The approach used to compile this map is based on the premise that ecological regions can be identified through the analysis of patterns of biotic and abiotic phenomena, including geology, physiography, vegetation, climate, soils, land use, wildlife, and hydrology. The relative importance of each characteristic varies from one ecological region to another. A Roman numeral hierarchical scheme has been adopted for different levels for ecological regions. Level I is the coarsest level, dividing North America into 15 ecological regions. Level II divides the continent into 50 regions (Commission for Environmental Cooperation Working Group, 1997). At Level III, the continental United States contains 105 regions whereas the conterminous United States has 85 (U.S. Environmental Protection Agency, 2011). Level IV ecoregions are further subdivisions of Level III eco

  2. Level IV Ecoregions of Oklahoma

    EPA Pesticide Factsheets

    Ecoregions by state were extracted from the seamless national shapefile. Ecoregions denote areas of general similarity in ecosystems and in the type, quality, and quantity of environmental resources. They are designed to serve as a spatial framework for the research, assessment, management, and monitoring of ecosystems and ecosystem components. These general purpose regions are critical for structuring and implementing ecosystem management strategies across federal agencies, state agencies, and nongovernment organizations that are responsible for different types of resources within the same geographical areas. The approach used to compile this map is based on the premise that ecological regions can be identified through the analysis of patterns of biotic and abiotic phenomena, including geology, physiography, vegetation, climate, soils, land use, wildlife, and hydrology. The relative importance of each characteristic varies from one ecological region to another. A Roman numeral hierarchical scheme has been adopted for different levels for ecological regions. Level I is the coarsest level, dividing North America into 15 ecological regions. Level II divides the continent into 50 regions (Commission for Environmental Cooperation Working Group, 1997). At Level III, the continental United States contains 105 regions whereas the conterminous United States has 85 (U.S. Environmental Protection Agency, 2011). Level IV ecoregions are further subdivisions of Level III eco

  3. Level IV Ecoregions of Wisconsin

    EPA Pesticide Factsheets

    Ecoregions by state were extracted from the seamless national shapefile. Ecoregions denote areas of general similarity in ecosystems and in the type, quality, and quantity of environmental resources. They are designed to serve as a spatial framework for the research, assessment, management, and monitoring of ecosystems and ecosystem components. These general purpose regions are critical for structuring and implementing ecosystem management strategies across federal agencies, state agencies, and nongovernment organizations that are responsible for different types of resources within the same geographical areas. The approach used to compile this map is based on the premise that ecological regions can be identified through the analysis of patterns of biotic and abiotic phenomena, including geology, physiography, vegetation, climate, soils, land use, wildlife, and hydrology. The relative importance of each characteristic varies from one ecological region to another. A Roman numeral hierarchical scheme has been adopted for different levels for ecological regions. Level I is the coarsest level, dividing North America into 15 ecological regions. Level II divides the continent into 50 regions (Commission for Environmental Cooperation Working Group, 1997). At Level III, the continental United States contains 105 regions whereas the conterminous United States has 85 (U.S. Environmental Protection Agency, 2011). Level IV ecoregions are further subdivisions of Level III eco

  4. Level IV Ecoregions of Nebraska

    EPA Pesticide Factsheets

    Ecoregions by state were extracted from the seamless national shapefile. Ecoregions denote areas of general similarity in ecosystems and in the type, quality, and quantity of environmental resources. They are designed to serve as a spatial framework for the research, assessment, management, and monitoring of ecosystems and ecosystem components. These general purpose regions are critical for structuring and implementing ecosystem management strategies across federal agencies, state agencies, and nongovernment organizations that are responsible for different types of resources within the same geographical areas. The approach used to compile this map is based on the premise that ecological regions can be identified through the analysis of patterns of biotic and abiotic phenomena, including geology, physiography, vegetation, climate, soils, land use, wildlife, and hydrology. The relative importance of each characteristic varies from one ecological region to another. A Roman numeral hierarchical scheme has been adopted for different levels for ecological regions. Level I is the coarsest level, dividing North America into 15 ecological regions. Level II divides the continent into 50 regions (Commission for Environmental Cooperation Working Group, 1997). At Level III, the continental United States contains 105 regions whereas the conterminous United States has 85 (U.S. Environmental Protection Agency, 2011). Level IV ecoregions are further subdivisions of Level III eco

  5. Level IV Ecoregions of Idaho

    EPA Pesticide Factsheets

    Ecoregions by state were extracted from the seamless national shapefile. Ecoregions denote areas of general similarity in ecosystems and in the type, quality, and quantity of environmental resources. They are designed to serve as a spatial framework for the research, assessment, management, and monitoring of ecosystems and ecosystem components. These general purpose regions are critical for structuring and implementing ecosystem management strategies across federal agencies, state agencies, and nongovernment organizations that are responsible for different types of resources within the same geographical areas. The approach used to compile this map is based on the premise that ecological regions can be identified through the analysis of patterns of biotic and abiotic phenomena, including geology, physiography, vegetation, climate, soils, land use, wildlife, and hydrology. The relative importance of each characteristic varies from one ecological region to another. A Roman numeral hierarchical scheme has been adopted for different levels for ecological regions. Level I is the coarsest level, dividing North America into 15 ecological regions. Level II divides the continent into 50 regions (Commission for Environmental Cooperation Working Group, 1997). At Level III, the continental United States contains 105 regions whereas the conterminous United States has 85 (U.S. Environmental Protection Agency, 2011). Level IV ecoregions are further subdivisions of Level III eco

  6. Level IV Ecoregions of Utah

    EPA Pesticide Factsheets

    Ecoregions by state were extracted from the seamless national shapefile. Ecoregions denote areas of general similarity in ecosystems and in the type, quality, and quantity of environmental resources. They are designed to serve as a spatial framework for the research, assessment, management, and monitoring of ecosystems and ecosystem components. These general purpose regions are critical for structuring and implementing ecosystem management strategies across federal agencies, state agencies, and nongovernment organizations that are responsible for different types of resources within the same geographical areas. The approach used to compile this map is based on the premise that ecological regions can be identified through the analysis of patterns of biotic and abiotic phenomena, including geology, physiography, vegetation, climate, soils, land use, wildlife, and hydrology. The relative importance of each characteristic varies from one ecological region to another. A Roman numeral hierarchical scheme has been adopted for different levels for ecological regions. Level I is the coarsest level, dividing North America into 15 ecological regions. Level II divides the continent into 50 regions (Commission for Environmental Cooperation Working Group, 1997). At Level III, the continental United States contains 105 regions whereas the conterminous United States has 85 (U.S. Environmental Protection Agency, 2011). Level IV ecoregions are further subdivisions of Level III eco

  7. Level IV Ecoregions of Kansas

    EPA Pesticide Factsheets

    Ecoregions by state were extracted from the seamless national shapefile. Ecoregions denote areas of general similarity in ecosystems and in the type, quality, and quantity of environmental resources. They are designed to serve as a spatial framework for the research, assessment, management, and monitoring of ecosystems and ecosystem components. These general purpose regions are critical for structuring and implementing ecosystem management strategies across federal agencies, state agencies, and nongovernment organizations that are responsible for different types of resources within the same geographical areas. The approach used to compile this map is based on the premise that ecological regions can be identified through the analysis of patterns of biotic and abiotic phenomena, including geology, physiography, vegetation, climate, soils, land use, wildlife, and hydrology. The relative importance of each characteristic varies from one ecological region to another. A Roman numeral hierarchical scheme has been adopted for different levels for ecological regions. Level I is the coarsest level, dividing North America into 15 ecological regions. Level II divides the continent into 50 regions (Commission for Environmental Cooperation Working Group, 1997). At Level III, the continental United States contains 105 regions whereas the conterminous United States has 85 (U.S. Environmental Protection Agency, 2011). Level IV ecoregions are further subdivisions of Level III eco

  8. Level IV Ecoregions of Colorado

    EPA Pesticide Factsheets

    Ecoregions by state were extracted from the seamless national shapefile. Ecoregions denote areas of general similarity in ecosystems and in the type, quality, and quantity of environmental resources. They are designed to serve as a spatial framework for the research, assessment, management, and monitoring of ecosystems and ecosystem components. These general purpose regions are critical for structuring and implementing ecosystem management strategies across federal agencies, state agencies, and nongovernment organizations that are responsible for different types of resources within the same geographical areas. The approach used to compile this map is based on the premise that ecological regions can be identified through the analysis of patterns of biotic and abiotic phenomena, including geology, physiography, vegetation, climate, soils, land use, wildlife, and hydrology. The relative importance of each characteristic varies from one ecological region to another. A Roman numeral hierarchical scheme has been adopted for different levels for ecological regions. Level I is the coarsest level, dividing North America into 15 ecological regions. Level II divides the continent into 50 regions (Commission for Environmental Cooperation Working Group, 1997). At Level III, the continental United States contains 105 regions whereas the conterminous United States has 85 (U.S. Environmental Protection Agency, 2011). Level IV ecoregions are further subdivisions of Level III eco

  9. Level IV Ecoregions of Oregon

    EPA Pesticide Factsheets

    Ecoregions by state were extracted from the seamless national shapefile. Ecoregions denote areas of general similarity in ecosystems and in the type, quality, and quantity of environmental resources. They are designed to serve as a spatial framework for the research, assessment, management, and monitoring of ecosystems and ecosystem components. These general purpose regions are critical for structuring and implementing ecosystem management strategies across federal agencies, state agencies, and nongovernment organizations that are responsible for different types of resources within the same geographical areas. The approach used to compile this map is based on the premise that ecological regions can be identified through the analysis of patterns of biotic and abiotic phenomena, including geology, physiography, vegetation, climate, soils, land use, wildlife, and hydrology. The relative importance of each characteristic varies from one ecological region to another. A Roman numeral hierarchical scheme has been adopted for different levels for ecological regions. Level I is the coarsest level, dividing North America into 15 ecological regions. Level II divides the continent into 50 regions (Commission for Environmental Cooperation Working Group, 1997). At Level III, the continental United States contains 105 regions whereas the conterminous United States has 85 (U.S. Environmental Protection Agency, 2011). Level IV ecoregions are further subdivisions of Level III eco

  10. Mass, nutrient pool, and mineralization of litter and fine roots in a tropical mountain cloud forest.

    PubMed

    Campos C, Adolfo; Cruz H, Lourdes; Rocha O, Sandra

    2017-01-01

    We used fine root and litter mass from a tropical mountain cloud forest to assess their relative contribution to nutrient content and to examine mineralization processes during a laboratory incubation experiment. Our results showed that average fine root mass density ranged from 2.86kgm(-3) to 11.59kgm(-3), while litter mass density ranged from 72.5kgm(-3) to 177.3kgm(-3). On average, fine root mass density represented 4.7% of the mass density of the O horizon. Fine root mass density followed an exponentially declining trend with soil depth. On average, 83% of fine root mass density within the soil profile was concentrated in the O horizon. Mean element pools in litter decreased from 44.08mgcm(-3) to 0.49μgcm(-3) in the following sequence: C>N>Fe>S>Ca>P>K>Mg>Na>Mn>Zn>Cu. For fine roots, a different mean element pool sequence (C>N>Ca>K>Fe>S>Mg>Na>P>Mn>Zn>Cu) in decreasing abundance (from 2.88mgcm(-3) to 0.13μgcm(-3)) was observed with respect to litter. Regarding C, litter mineralized faster than fine roots, with a mean k value of 0.25d(-1) for litter and 0.13d(-1) for fine roots. Principal component analysis (PCA) combined with stepwise regression analysis revealed that the main mass density predictors were N, S, Zn, and Mn for litter (p<0.0001, R(2)=0.92), and S and C/N ratio for fine roots (p<0.0001, R(2)=0.82). These results demonstrate the potential of chemical composition to influence the mineralization of fine root and litter mass and therefore the nutrient availability and C sequestration.

  11. Get out of Fines Free: Recruiting Student Usability Testers via Fine Waivers

    ERIC Educational Resources Information Center

    Hockenberry, Benjamin; Blackburn, Kourtney

    2016-01-01

    St. John Fisher College's Lavery Library's Access Services and Systems departments began a pilot project in which students with overdue fines tested usability of library Web sites in exchange for fine waivers. Circulation staff promoted the program and redeemed fine waiver vouchers at the Checkout Desk, while Systems staff administered testing and…

  12. The Relationship between Fine-Motor Play and Fine-Motor Skill

    ERIC Educational Resources Information Center

    Marr, Deborah; Cermak, Sharon; Cohn, Ellen S.; Henderson, Anne

    2004-01-01

    This study examined the relationship between free-play choices and fine-motor skill in 4-year-old children attending Head Start. Children with poor fine-motor skill were matched for age and gender with children in the same classroom that exhibited good fine-motor skill. Each pair was observed during free-play sessions to examine the degree of…

  13. Get out of Fines Free: Recruiting Student Usability Testers via Fine Waivers

    ERIC Educational Resources Information Center

    Hockenberry, Benjamin; Blackburn, Kourtney

    2016-01-01

    St. John Fisher College's Lavery Library's Access Services and Systems departments began a pilot project in which students with overdue fines tested usability of library Web sites in exchange for fine waivers. Circulation staff promoted the program and redeemed fine waiver vouchers at the Checkout Desk, while Systems staff administered testing and…

  14. Fine Structure of Plasmaspheric Hiss

    NASA Astrophysics Data System (ADS)

    Summers, D.; Omura, Y.; Nakamura, S.; Kletzing, C.

    2014-12-01

    Plasmaspheric hiss plays a key role in controlling the structure and dynamics of Earth's radiation belts.The quiet time slot region between the inner and outer belts can be explained as a steady-state balance between earthward radial diffusion and pitch-angle scattering loss of energetic electrons to the atmosphere induced by plasmaspheric hiss. Plasmaspheric hiss can also induce gradual precipitation loss of MeV electrons from the outer radiation belt. Plasmaspheric hiss has been widely regarded as a broadband,structureless,incoherent emission. Here, by examining burst-mode vector waveform data from the EMFISIS instrument on the Van Allen Probes mission,we show that plasmaspheric hiss is a coherent emission with complex fine structure. Specifically, plasmaspheric hiss appears as discrete rising tone and falling tone elements. By means of waveform analysis we identify typical amplitudes,phase profiles,and sweep rates of the rising and falling tone elements. The new observations reported here can be expected to fuel a re-examination of the properties of plasmaspheric hiss, including a further re-analysis of the generation mechanism for hiss.

  15. Fine Structure of Thiobacillus thiooxidans.

    PubMed

    Mahoney, R P; Edwards, M R

    1966-08-01

    Mahoney, Robert P. (Skidmore College, Saratoga Springs, N.Y.), and Mercedes R. Edwards. Fine structure of Thiobacillus thiooxidans. J. Bacteriol. 92: 487-495. 1966.-Thin section analysis of the chemosynthetic autotroph Thiobacillus thiooxidans revealed structures comparable to gram-negative heterotrophic bacteria. Although this species is unique in that it oxidizes elemental sulfur for energy, uses carbon dioxide as its sole source of carbon, and can withstand a pH of less than 1, thin sections revealed a profile of the cell envelope (cell wall and plasmalemma) similar to other gram-negative species which have more common physiological traits. The cell wall is composed of five layers with an overall width of approximately 200 A, and the plasmalemma appears as a conventional "unit membrane" with a width of about 85 A. Volutin granules and less-dense bodies of similar shape and size were frequently observed in close association with the nucleoplasm. The nature and function of these bodies are unknown at this time.

  16. SOUTHERN FINE PARTICULATE MONITORING PROJECT

    SciTech Connect

    Unknown

    2002-04-01

    This quarterly report presents results and analysis of continuous onsite ambient fine particulate data at the North Birmingham sampling site during the January-March, 2002 study period. The continuous data include PM{sub 2.5} mass concentrations measured by TEOM, particle sulfate using the R&P 8400S monitor, particle size distributions measured by SMPS and APS monitors, and PM{sub 2.5} light scattering extinction coefficient as measured by nephelometer. Some instrumental issues were noted with the upgrade of the APS model 3320 are described in the report, as well as preliminary performance indications for the upgraded instrument. During the quarter preliminary data analysis and modeling studies were conducted to test the potential of the North Birmingham site data for source attribution analyses. Our initial assessment has continued to be optimistic in this regard due to the location of the site relative to several important classes of local and midrange emission sources. We anticipate that these analyses will provide good separations of the effects of major source classes and spatial source clusters, and will provide useful information relevant to PM{sub 2.5} implementation strategies.

  17. Cognitive and Adaptive Skills in Toddlers Who Meet Criteria for Autism in DSM-IV but not DSM-5.

    PubMed

    Jashar, Dasal Tenzin; Brennan, Laura A; Barton, Marianne L; Fein, Deborah

    2016-12-01

    The current study compared adaptive and cognitive skills, and autism severity of toddlers with an autism spectrum disorder (ASD) diagnosis under DSM-IV but not DSM-5 criteria (DSM-IV only group) to those who met autism criteria under both diagnostic systems (DSM-5 group) and to those without ASD (non-ASD group). The toddlers in the DSM-IV only group were less delayed on various domains of adaptive (Communication, Socialization) and cognitive (Expressive and Receptive language, Fine Motor, Visual Reception) skills, and had less severe symptoms of ASD than the DSM-5 group. Thus, they might have the best potential for successful intervention. The DSM-IV only group did not differ from the non-ASD group in any adaptive or cognitive skills except for socialization skills, the hallmark of ASD.

  18. Fine-Sediment Loadings to Lake Tahoe

    USDA-ARS?s Scientific Manuscript database

    Over the past 35 years, a trend of decreasing water clarity has been documented in Lake Tahoe, attributable in part to the delivery of fine-grained sediments emanating from upland and channel sources. The overall objective of the research reported here was to determine the amount of fine sediment de...

  19. ADVANCING FINE ROOT RESEARCH WITH MINIRHIZOTRONS

    EPA Science Inventory

    Minirhizotrons provide a nondestructive, in situ method for directly viewing and studying fine roots. Although many insights into fine roots have been gained using minirhizotrons, it is clear from the literature that there is still wide variation in how minirhizotrons and minirhi...

  20. 47 CFR 76.943 - Fines.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... TELEVISION SERVICE Cable Rate Regulation § 76.943 Fines. (a) A franchising authority may impose fines or monetary forfeitures on a cable operator that does not comply with a rate decision or refund order directed.... (b) If a cable operator willfully fails to comply with the terms of any franchising authority's order...

  1. ADVANCING FINE ROOT RESEARCH WITH MINIRHIZOTRONS

    EPA Science Inventory

    Minirhizotrons provide a nondestructive, in situ method for directly viewing and studying fine roots. Although many insights into fine roots have been gained using minirhizotrons, it is clear from the literature that there is still wide variation in how minirhizotrons and minirhi...

  2. Legal Rights of the Fine Artist.

    ERIC Educational Resources Information Center

    Millinger, Donald M.

    1980-01-01

    Examines the current status and changing patterns of copyrights, resale royalty rights, and moral rights that have the potential of according the fine artist greater protection and economic security. Discusses an existing California law as a model for protection of the fine artists' moral rights. (JMF)

  3. Metsahovi Radio Observatory - IVS Network Station

    NASA Technical Reports Server (NTRS)

    Uunila, Minttu; Zubko, Nataliya; Poutanen, Markku; Kallunki, Juha; Kallio, Ulla

    2013-01-01

    In 2012, Metsahovi Radio Observatory together with Finnish Geodetic Institute officially became an IVS Network Station. Eight IVS sessions were observed during the year. Two spacecraft tracking and one EVN X-band experiment were also performed. In 2012, the Metsahovi VLBI equipment was upgraded with a Digital Base Band Converter, a Mark 5B+, a FILA10G, and a FlexBuff.

  4. IVS Working Group 4: VLBI Data Structures

    NASA Technical Reports Server (NTRS)

    Gipson, John

    2010-01-01

    In 2007 the IVS Directing Board established IVS Working Group 4 on VLBI Data Structures. This note discusses the current VLBI data format, goals for a new format, the history and formation of the Working Group, and a timeline for the development of a new VLBI data format.

  5. CHLORINE ABSORPTION IN S(IV) SOLUTIONS

    EPA Science Inventory

    The report gives results of measurements of the rate of Chlorine (Cl2) absorption into aqueous sulfite/bisulfite -- S(IV) -- solutions at ambient temperature using a highly characterized stirred-cell reactor. The reactor media were 0 to 10 mM S(IV) with pHs of 3.5-8.5. Experiment...

  6. Improving Detection of IV Infiltrates in Neonates

    PubMed Central

    Driscoll, MD, Colleen; Langer, Melissa; Burke, Susan; El Metwally, MD, Dina

    2015-01-01

    Neonates and infants in the neonatal intensive care unit suffer significant morbidity when intravenous (IV) catheters infiltrate. The underreporting of adverse events through hospital voluntary reporting systems, such as ours, can complicate the monitoring of low incidence events, like IV infiltrates. Based on severe cases of IV infiltrates observed in our neonatal intensive care unit, we attempted to improve the detection of all infiltrates and reduce the incidence of Stage 4 infiltrates. We developed, and initiated the use of, an evidence-based guideline for the improved surveillance, prevention, and management of IV infiltrates, with corresponding educational interventions for faculty and staff. We instituted the use of a checklist for compliance with guidelines, and as a mechanism of surveillance. The baseline incidence rate of IV infiltrates, determined by the voluntary reporting system, was 5 per 1000 line days. Following initiation of the guidelines and checklist, the IV infiltrate rate increased to 9 per 1000 line days. In most months, the detection of IV infiltrates was improved by use of the checklist. During the post-intervention period the rate of Stage 4 infiltrates, as measured by usage of nitroglycerin ointment, was significantly reduced. In conclusion, the detection of IV infiltrates was improved following our quality improvement interventions. Further, use of an evidence-based guideline for managing infiltrates may reduce the most severe infiltrate injuries. PMID:26734388

  7. CHLORINE ABSORPTION IN S(IV) SOLUTIONS

    EPA Science Inventory

    The report gives results of measurements of the rate of Chlorine (Cl2) absorption into aqueous sulfite/bisulfite -- S(IV) -- solutions at ambient temperature using a highly characterized stirred-cell reactor. The reactor media were 0 to 10 mM S(IV) with pHs of 3.5-8.5. Experiment...

  8. 24 CFR Appendixes I-Iv to Subpart B - Appendixes I-IV to Subpart B

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 24 Housing and Urban Development 4 2012-04-01 2012-04-01 false Appendixes I-IV to Subpart B I Appendixes I-IV to Subpart B Housing and Urban Development REGULATIONS RELATING TO HOUSING AND URBAN... Appendixes I-IV to Subpart B Appendix I—Annual Contributions Contract “Special Provisions for Turnkey...

  9. 24 CFR Appendixes I-Iv to Subpart B - Appendixes I-IV to Subpart B

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 24 Housing and Urban Development 4 2014-04-01 2014-04-01 false Appendixes I-IV to Subpart B I Appendixes I-IV to Subpart B Housing and Urban Development REGULATIONS RELATING TO HOUSING AND URBAN... Appendixes I-IV to Subpart B Appendix I—Annual Contributions Contract “Special Provisions for Turnkey...

  10. NATIONAL COASTAL CONDITION REPORT IV | Science ...

    EPA Pesticide Factsheets

    The National Coastal Condition Report IV (NCCR IV) is the fourth in a series of environmental assessments of U.S. coastal waters and the Great Lakes. The report includes assessments of all the nation’s estuaries in the contiguous 48 states and Puerto Rico, south-eastern Alaska, Hawaii, the U.S. Virgin Islands, Guam, and American Samoa. The NCCR IV presents four main types of data: (1) coastal monitoring data, (2) coastal ocean/ offshore monitoring data, (3) offshore fisheries data, and (4) assessment and advisory data (new to NCCR IV). The NCCR IV relies heavily on coastal monitoring data from EPA’s National Coastal Assessment (NCA) to assess coastal condition by evaluating five indicators of condition—water quality, sediment quality, benthic community condition, coastal habitat loss, and fish tissue contaminants. To assess and report on the condition of the nation's coastal resources

  11. Biospeciation of various antidiabetic V(IV)O compounds in serum.

    PubMed

    Jakusch, Tamás; Hollender, Dominik; Enyedy, Eva Anna; González, Cristina Sánchez; Montes-Bayón, Maria; Sanz-Medel, Alfredo; Costa Pessoa, João; Tomaz, Isabel; Kiss, Tamás

    2009-04-07

    The interactions of various insulin mimetic oxovanadium(IV) compounds with serum proteins were studied in model systems and in ex vivo samples. For the modeling study, an earlier in situ method was extended and applied to the formation of ternary complexes of apotransferrin (apoTf)-V(IV)O-maltol (mal) and 1,2-dimethyl-3-hydroxy-4(1H)-pyridinone (dhp). Both systems were evaluated via simultaneous CD and EPR measurements. Determination of the formation constants of the ternary complexes allowed the calculation of more accurate stability constants for the V(IV)O-apoTf parent complexes and establishment of a better model for drug speciation in serum. It was found that dhp and the synergistic carbonate are non-competitive binders. Based on the stability constants obtained for V(IV)O-apoTf complexes and estimated for V(IV)O-HSA (= human serum albumin), modeling calculations were performed on the distribution of V(IV)O among the components of blood serum. The results were confirmed by HPLC-ICP-MS (liquid chromatography-inductively coupled plasma spectroscopy-mass spectrometry) measurements. The ex vivo interactions of the V(IV)O complexes formed with mal, picolinic acid (pic) and dhp with serum protein standards and also with human serum samples were evaluated. The proteins were firstly separated by (HPLC), and the V content of each fraction was determined by ICP-MS. All the studied V(IV)O compounds displayed similar chromatographic profiles, associated almost exclusively with apotransferrin as predicted by the modeling calculations. Under physiological conditions, the interactions with HSA of all of the species under study were negligible. Therefore Tf seems to be the main V(IV)O transporter in the serum under in vitro conditions, and this association is practically independent of the chemical form in which V(IV)O is administered.

  12. Modifying the properties of finely ground limestone by tumbling granulation

    NASA Astrophysics Data System (ADS)

    Macho, Oliver; Eckert, Maroš; Tomášová, Barbora; Peciar, Peter; Ščasný, Martin; Fekete, Roman; Peciar, Marián

    2016-06-01

    Calcium carbonate in the form of finely ground limestone is a material that has found its application in a wide range of industries, in the chemical, rubber, agricultural, and paper industries, is used for desulfurization of boilers and other. In civil engineering, ground limestone is used for the production of building materials, plaster and mortar mixtures, as a filler in concrete mixtures, in road construction, and as an essential component of mastic asphalt. This paper deals with examining the modification of the properties of finely ground limestone by the tumbling agglomeration method. It has been shown that the components of concrete with a round grain have a positive effect on the pumping of concrete in comparison with an elongated grain or the rough surface of crushed stone. The experiments will be carried out on a granulation plate using a variety of granulation liquid. The agglomerates and their properties were compared with untreated finely ground limestone, with a focus on detecting changes in compressibility, density and particle size. The output of this paper is a description and graphical representation of the changes in the properties of ground limestone before and after the agglomeration process.

  13. Autonomous patterning of cells on microstructured fine particles.

    PubMed

    Takeda, Iwori; Kawanabe, Masato; Kaneko, Arata

    2015-05-01

    Regularly patterned cells can clarify cellular function and are required in some biochip applications. This study examines cell patterning along microstructures and the effect of microstructural geometry on selective cellular adhesion. Particles can be autonomously assembled on a soda-lime glass substrate that is chemically patterned by immersion in a suspension of fine particles. By adopting various sizes of fine particles, we can control the geometry of the microstructure. Cells adhere more readily to microstructured fine particles than to flat glass substrate. Silica particles hexagonally packed in 5-40 μm line and space microstructures provide an effective cell scaffold on the glass substrate. Cultured cells tend to attach and proliferate along the microstructured region while avoiding the flat region. The difference in cell adhesion is attributed to their geometries, as both of the silica particles and soda-lime glass are hydrophilic related with cell adhesiveness. After cell seeding, cells adhered to the flat region migrated toward the microstructured region. For most of the cells to assemble on the scaffold, the scaffolding microstructures must be spaced by at most 65 μm. Copyright © 2015 Elsevier B.V. All rights reserved.

  14. Quantitative separation of monomeric U(IV) from UO2 in products of U(VI) reduction

    PubMed Central

    Alessi, Daniel S.; Uster, Benjamin; Veeramani, Harish; Suvorova, Elena I.; Lezama-Pacheco, Juan S.; Stubbs, Joanne E.; Bargar, John R.; Bernier-Latmani, Rizlan

    2012-01-01

    The reduction of soluble hexavalent uranium to tetravalent uranium can be catalyzed by bacteria and minerals. The end-product of this reduction is often the mineral uraninite, which was long assumed to be the only product of U(VI) reduction. However, recent studies report the formation of other species including an adsorbed U(IV) species, operationally referred to as monomeric U(IV). The discovery of monomeric U(IV) is important because the species is likely to be more labile and more susceptible to reoxidation than uraninite. Because there is a need to distinguish between these two U(IV) species, we propose here a wet chemical method of differentiating monomeric U(IV) from uraninite in environmental samples. To calibrate the method, U(IV) was extracted from known mixtures of uraninite and monomeric U(IV) and testted using X-ray absorption spectroscopy (XAS). Monomeric U(IV) was efficiently removed from biomass and Fe(II)-bearing phases by bicarbonate extraction, without affecting uraninite stability. After confirming that the method effectively separates monomeric U(IV) and uraninite, it is further evaluated for a system containing those reduced U species and adsorbed U(VI). The method provides a rapid complement, and in some cases alternative, to XAS analyses for quantifying monomeric U(IV), uraninite, and adsorbed U(VI) species in environmental samples. PMID:22540966

  15. Quantitative separation of monomeric U(IV) from UO2 in products of U(VI) reduction.

    PubMed

    Alessi, Daniel S; Uster, Benjamin; Veeramani, Harish; Suvorova, Elena I; Lezama-Pacheco, Juan S; Stubbs, Joanne E; Bargar, John R; Bernier-Latmani, Rizlan

    2012-06-05

    The reduction of soluble hexavalent uranium to tetravalent uranium can be catalyzed by bacteria and minerals. The end-product of this reduction is often the mineral uraninite, which was long assumed to be the only product of U(VI) reduction. However, recent studies report the formation of other species including an adsorbed U(IV) species, operationally referred to as monomeric U(IV). The discovery of monomeric U(IV) is important because the species is likely to be more labile and more susceptible to reoxidation than uraninite. Because there is a need to distinguish between these two U(IV) species, we propose here a wet chemical method of differentiating monomeric U(IV) from uraninite in environmental samples. To calibrate the method, U(IV) was extracted from known mixtures of uraninite and monomeric U(IV) and tested using X-ray absorption spectroscopy (XAS). Monomeric U(IV) was efficiently removed from biomass and Fe(II)-bearing phases by bicarbonate extraction, without affecting uraninite stability. After confirming that the method effectively separates monomeric U(IV) and uraninite, it is further evaluated for a system containing those reduced U species and adsorbed U(VI). The method provides a rapid complement, and in some cases alternative, to XAS analyses for quantifying monomeric U(IV), uraninite, and adsorbed U(VI) species in environmental samples.

  16. Influence of addition order and contact time on thorium(IV) retention by hematite in the presence of humic acids.

    PubMed

    Reiller, Pascal; Casanova, Florence; Moulin, Valérie

    2005-03-15

    The influence of addition order and contact time in the system hematite (alpha-Fe2O3)-humic acid (HA)-thorium(IV) (Th(IV)) was studied in batch experiments. Th(IV) is considered here as a chemical analogue of other actinides (IV). The sorption isotherms were acquired varying pH in the range 2-10 and HA concentration in the range 1-100 mg/L. As already observed by numerous authors, Th(IV) retention was hindered when HA and hematite were equilibrated beforehand during 24 h. As it has been observed in a previous study, this effect was drastic when the ratio between humic and surface (iron oxide) sites exceeds a critical value. However, when HA was added after a 24-h equilibration of the hematite-Th(IV) system, Th(IV) was barely desorbed from the iron oxide surface. Furthermore, no drastic effect of the ratio between humic and surface sites could be evidenced, as the increase of HA concentration only results in a slight monotonic decrease in Th(IV) retention. Increasing contact time between components of the systems only indicated slight Th(IV) retention variation. This was interpreted as a consequence of slow kinetic controls of both the Th(IV)-HA complexation and HA-hematite sorption.

  17. STUDIES IN METABOLIC SPECTRA IV.

    PubMed Central

    Cheng, Lorraine; Snell, J. F.

    1962-01-01

    Cheng, Lorraine (Radiobiochemistry Department, Chas. Pfizer & Co., Inc., Maywood, N. J.) and J. F. Snell. Studies in metabolic spectra. IV. Effects of tetracyclines, some of their derivatives, and chloramphenicol on accumulation of glutamic acid in Escherichia coli. J. Bacteriol. 83:711–719. 1962.—Escherichia coli strain 21 was incubated in the Warburg apparatus at 37 C with sodium acetate-2-C14 and 0.1 μmole/ml of various test compounds. Up to 1 hr, de novo C14-glutamic acid (synthesized from the C14-acetate precursor) accumulation in the fermentation broth was found to be a common phenomenon for the control cells and cells treated with oxytetracycline, chlortetracycline, tetracycline, and chloramphenicol. Subsequently, C14-glutamic acid continued to accumulate in the broth of the inhibited cells, but began to disappear from the broth of the control cells. During the first half hour, the rate of accumulation was most rapid in the presence of oxytetracycline. At 3 hr the total de nova C14-glutamic acid was found to be the same whether cells were treated with oxytetracycline or not. However, the distribution of this glutamic acid was different. In the oxytetracycline-treated cells, more than 87% of the total de nova C14-glutamic acid was in the broth, and only 13% was incorporated into the cell residue. In the control cells, no C14-glutamic acid was found in the broth, although 67% was in the cell residue. The possibility that the tetracyclines and chloramphenicol have different modes of action, and that oxytetracycline inhibits the incorporation of d-glutamic acid into the cell wall and membrane material in E. coli 21, was discussed. PMID:13878663

  18. Chemical Properties of Combustion Aerosols: An Overview

    EPA Science Inventory

    A wide variety of pyrogenic and anthropogenic sources emit fine aerosols to the atmosphere. The physical and chemical properties of these aerosols are of interest due to their influence on climate, human health, and visibility. Aerosol chemical composition is remarkably complex. ...

  19. Chemical Properties of Combustion Aerosols: An Overview

    EPA Science Inventory

    A wide variety of pyrogenic and anthropogenic sources emit fine aerosols to the atmosphere. The physical and chemical properties of these aerosols are of interest due to their influence on climate, human health, and visibility. Aerosol chemical composition is remarkably complex. ...

  20. Oil sands fine tailings - a resource material for potentially marketable products

    SciTech Connect

    Majid, A.; Sparks, B.D.; Coleman, R.D.

    1995-12-31

    Oil sands fine tailings is a complex mixture of components each having specific physical or chemical characteristics. Studies on the fundamental properties of fine tailings have resulted in the development of methods to fractionate the tailings into products with market potential. These include: bitumen, for production of synthetic crude oil or as an ancillary fuel; clean kaolin for fine paper coating; a gelling agent for drilling mud formulation; emulsifying solids, for surfactant replacement; and a mineral fraction, for heavy metal recovery. In this investigation we have attempted to evaluate the economic potential of fine tailings as a resource material by determining the amount and value of these products; the prime objective was to determine the economic feasibility of a tailings treatment scheme.

  1. Source apportionment of airborne fine particulate matter in an underground mine.

    PubMed

    McDonald, Jacob D; Zielinska, Barbara; Sagebiel, John C; McDaniel, Mark R; Mousset-Jones, Pierre

    2003-04-01

    The chemical mass balance source apportionment technique was applied to an underground gold mine to assess the contribution of diesel exhaust, rock dust, oil mists, and cigarette smoke to airborne fine (<2.5 microm) particulate matter (PM). Apportionments were conducted in two locations in the mine, one near the mining operations and one near the exit of the mine where the ventilated mine air was exhausted. Results showed that diesel exhaust contributed 78-98% of the fine particulate mass and greater than 90% of the fine particle carbon, with rock dust making up the remainder. Oil mists and cigarette smoke contributions were below detection limits for this study. The diesel exhaust fraction of the total fine PM was higher than the recently implemented mine air quality standards based on total carbon at both sample locations in the mine.

  2. Comparison of sulfur measurements from a regional fine particle network with concurrent acid modes network results

    SciTech Connect

    Bennett, R.L.; Stockburger, L.; Barnes, H.M.

    1994-01-01

    The Fine Particle Network (FPN), a system of fine particle (less than 2.5 micrometers) samplers, was operated at 41 sites selected from the Enviromental Protection Agency Acid MODES program during the two year period in 1988-90. The 24-hour sample results included fine particle mass and the most predominant chemical element concentrations determined by wavelength dispersive x-ray fluorescence analysis. Statistical summaries of the fine mass and sulfur concentrations by site and season were prepared. The availability of simultaneous particulate sulfate measurements from independent collection and analytical procedures provided an opportunity to examine their agreement and provide a more reliable data base for evaluation of regional particulate models and estimation of contribution to urban aerosol concentration.

  3. Magnetofluidization of fine magnetite powder.

    PubMed

    Valverde, J M; Espin, M J; Quintanilla, M A S; Castellanos, A

    2009-03-01

    The behavior of a fluidized bed of fine magnetite particles as affected by a cross-flow magnetic field is investigated. A distinct feature of this naturally cohesive powder, as compared to noncohesive magnetic grains usually employed in magnetofluidized beds, is that the fluidized bed displays a range of stable fluidization even in the absence of an external magnetic field. Upon application of the magnetic field, the interval of stable fluidization is extended to higher gas velocities and bed expansion is enhanced. We have measured the tensile strength as affected by application of the external magnetic field according to two different operation modes. In the H off-on operation mode, the bed is driven to bubbling in the absence of external magnetic field. Once the gas velocity is decreased below the bubbling onset and the bed has returned to stable fluidization due to natural cohesive forces, the field is applied. In the H on-on mode, the field is maintained during the whole process of bubbling and return to stable fluidization. It is found that the tensile strength of the naturally stabilized bed is not essentially changed by application of the field ( H off-on) since the magnetic field cannot alter the bed structure once the particles are jammed in the stable fluidization state. Magnetic forces within the bulk of the jammed bed are partially canceled as a result of the anisotropic nature of the dipole-dipole interaction between the particles, which gives rise to just a small increment of the tensile strength. On the other hand, when the field is held on during bubbling and transition to stable fluidization ( H on-on mode), the tensile strength is appreciably increased. This suggests the formation of particle chains when the particles are not constrained due to the dipole-dipole attractive interaction which affects the mechanical strength of the stably fluidized bed. Experimental data are analyzed in the light of theoretical models on magnetic surface stresses.

  4. Paste mechanics for fine extrusion

    NASA Astrophysics Data System (ADS)

    Hurysz, Kevin Michael

    compositional range; (5) Shear zone behavior, and the influence and limitations the shear layer places on fine extrusion.

  5. ChemCam analysis of Martian fine dust

    NASA Astrophysics Data System (ADS)

    Lasue, Jeremie; Mangold, Nicolas; Cousin, Agnes; Meslin, Pierre-Yves; Wiens, Roger; Gasnault, Olivier; Rapin, William; Schroder, Susanne; Ollila, Ann; Fabre, Cécile; Berger, Gilles; Le Mouélic, Stéphane; Dehouck, Erwin; Forni, Olivier; Maurice, Sylvestre; Anderson, Ryan; Bridges, Nathan; Clark, Benton; Clegg, Samuel; d'Uston, Claude; Goetz, Walter; Johnson, Jeffrey R.; Lanza, Nina; Madsen, Morten; Melikechi, Noureddine; Newsom, Horton; Sautter, Violaine; Martin-Torres, Javier; Zorzano, Maria-Paz; MSL Science Team

    2016-10-01

    In this work, we examine the chemical composition of dust observed by the Chemistry Camera (ChemCam) instrument onboard the Mars Science Laboratory (MSL) rover at Gale Crater. The Laser Induced Breakdown Spectroscopy technique analyses samples without preparation, which allows detection of the elemental composition of surface deposits. Mars aeolian fine dust (<2-3 microns) composition is analyzed on the first shot of each Mars target. It is reproducible over time and present a composition characteristic of the global martian fine dust, which covers the entire planet and contributes to the local geology analyzed by MSL. Its composition can also be retrieved on the ChemCam Calibration Targets (CCCT) by subtraction of the well characterized CCCT spectra. The CCCT include eight glasses and ceramics that have been generated to simulate Martian rocks of interest and two targets of a single element (graphite for carbon and an alloy of titanium). ChemCam passive spectroscopy also indicates varying deposition of the dust cover on the CCCT.Major elements are quantified and shown to be very similar to the fine soils encountered at Gale crater. The composition is also similar to the soils and fine dust measured by APXS for the elements common to both instruments. The minor elements quantified by ChemCam (Ba, Sr, Rb, Li, Mn, Cr) are within the range of soil surveys, but we see a higher concentration of Li than in other types of remotely characterized targets. Sulfur is possibly detected at the ChemCam limit of detection. Hydrogen is clearly identified, indicating that this fine dust is a contributor to the H content of the martian soils, as also detected by the SAM and CheMin instruments, and provides constraints as to which fraction of the Martian surface is hydrated and altered. In conclusion, the finest fraction of dust particles on the surface of Mars contains hydrated components mixed intimately within the fine aeolian dust fraction, suggesting that this dust likely

  6. Fine Guidance Sensing for Coronagraphic Observatories

    NASA Technical Reports Server (NTRS)

    Brugarolas, Paul; Alexander, James W.; Trauger, John T.; Moody, Dwight C.

    2011-01-01

    Three options have been developed for Fine Guidance Sensing (FGS) for coronagraphic observatories using a Fine Guidance Camera within a coronagraphic instrument. Coronagraphic observatories require very fine precision pointing in order to image faint objects at very small distances from a target star. The Fine Guidance Camera measures the direction to the target star. The first option, referred to as Spot, was to collect all of the light reflected from a coronagraph occulter onto a focal plane, producing an Airy-type point spread function (PSF). This would allow almost all of the starlight from the central star to be used for centroiding. The second approach, referred to as Punctured Disk, collects the light that bypasses a central obscuration, producing a PSF with a punctured central disk. The final approach, referred to as Lyot, collects light after passing through the occulter at the Lyot stop. The study includes generation of representative images for each option by the science team, followed by an engineering evaluation of a centroiding or a photometric algorithm for each option. After the alignment of the coronagraph to the fine guidance system, a "nulling" point on the FGS focal point is determined by calibration. This alignment is implemented by a fine alignment mechanism that is part of the fine guidance camera selection mirror. If the star images meet the modeling assumptions, and the star "centroid" can be driven to that nulling point, the contrast for the coronagraph will be maximized.

  7. Surprising Coordination Geometry Differences in Ce(IV)- and Pu(IV)-Maltol Complexes

    SciTech Connect

    Lawrence Berkeley National Laboratory; Raymond, Kenneth; Szigethy, Geza; Xu, Jide; Gorden, Anne E.V.; Teat, Simon J.; Shuh, David K.; Raymond, Kenneth N.

    2008-02-12

    As part of a study to characterize the detailed coordination behavior of Pu(IV), single crystal X-ray diffraction structures have been determined for Pu(IV) and Ce(IV) complexes with the naturally-occurring ligand maltol (3-hydroxy-2-methyl-pyran-4-one) and its derivative bromomaltol (5-bromo-3-hydroxy-2-methyl-pyran-4-one). Although Ce(IV) is generally accepted as a structural analog for Pu(IV), and the maltol complexes of these two metals are isostructural, the corresponding bromomaltol complexes are strikingly different with respect to ligand orientation about the metal ion: All complexes exhibit trigonal dodecahedral coordination geometry but the Ce(IV)-bromomaltol complex displays an uncommon ligand arrangement not mirrored in the Pu(IV) complex, although the two metal species are generally accepted to be structural analogs.

  8. Oxyhydroxy Silicate Colloids: A New Type of Waterborne Actinide(IV) Colloids

    PubMed Central

    Weiss, Stephan; Hennig, Christoph; Brendler, Vinzenz; Ikeda‐Ohno, Atsushi

    2016-01-01

    Abstract At the near‐neutral and reducing aquatic conditions expected in undisturbed ore deposits or in closed nuclear waste repositories, the actinides Th, U, Np, and Pu are primarily tetravalent. These tetravalent actinides (AnIV) are sparingly soluble in aquatic systems and, hence, are often assumed to be immobile. However, AnIV could become mobile if they occur as colloids. This review focuses on a new type of AnIV colloids, oxyhydroxy silicate colloids. We herein discuss the chemical characteristics of these colloids and the potential implication for their environmental behavior. The binary oxyhydroxy silicate colloids of AnIV could be potentially more mobile as a waterborne species than the well‐known mono‐component oxyhydroxide colloids. PMID:27957406

  9. Synthesis, structure, and optoelectronic properties of II-IV-V2 materials

    DOE PAGES

    Martinez, Aaron D.; Fioretti, Angela N.; Toberer, Eric S.; ...

    2017-03-07

    II-IV-V2 materials offer the promise of enhanced functionality in optoelectronic devices due to their rich ternary chemistry. In this review, we consider the potential for new optoelectronic devices based on nitride, phosphide, and arsenide II-IV-V2 materials. As ternary analogs to the III-V materials, these compounds share many of the attractive features that have made the III-Vs the basis of modern optoelectronic devices (e.g. high mobility, strong optical absorption). Control of cation order parameter in the II-IV-V2 materials can produce significant changes in optoelectronic properties at fixed chemical composition, including decoupling band gap from lattice parameter. Recent progress has begun tomore » resolve outstanding questions concerning the structure, dopability, and optical properties of the II-IV-V2 materials. Furthermore, remaining research challenges include growth optimization and integration into heterostructures and devices.« less

  10. Development of Platinum(iv) Complexes as Anticancer Prodrugs: the Story so Far

    NASA Astrophysics Data System (ADS)

    Wong, Daniel Yuan Qiang; Ang, Wee Han

    2012-06-01

    The serendipitous discovery of the antitumor properties of cisplatin by Barnett Rosenberg some forty years ago brought about a paradigm shift in the field of medicinal chemistry and challenged conventional thinking regarding the role of potentially toxic heavy metals in drugs. Platinum(II)-based anticancer drugs have since become some of the most effective and widely-used drugs in a clinician's arsenal and have saved countless lives. However, they are limited by high toxicity, severe side-effects and the incidence of drug resistance. In recent years, attention has shifted to stable platinum(IV) complexes as anticancer prodrugs. By exploiting the unique chemical and structural attributes of their scaffolds, these platinum(IV) prodrugs offer new strategies of targeting and killing cancer cells. This review summarizes the development of anticancer platinum(IV) prodrugs to date and some of the exciting strategies that utilise the platinum(IV) construct as targeted chemotherapeutic agents against cancer.

  11. Actinide(IV) Deposits on Bone: Potential Role of the Osteopontin-Thorium Complex.

    PubMed

    Creff, Gaëlle; Safi, Samir; Roques, Jérôme; Michel, Hervé; Jeanson, Aurélie; Solari, Pier-Lorenzo; Basset, Christian; Simoni, Eric; Vidaud, Claude; Den Auwer, Christophe

    2016-01-04

    In case of a nuclear event, contamination (broad or limited) of the population or of specific workers might occur. In such a senario, the fate of actinide contaminants may be of first concern, in particular with regard to human target organs like the skeleton. To improve our understanding of the toxicological processes that might take place, a mechanistic approach is necessary. For instance, ∼50% of Pu(IV) is known from biokinetic data to accumulate in bone, but the underlining mechanisms are almost unknown. In this context, and to obtain a better description of the toxicological mechanisms associated with actinides(IV), we have undertaken the investigation, on a molecular scale, of the interaction of thorium(IV) with osteopontin (OPN) a hyperphosphorylated protein involved in bone turnover. Thorium is taken here as a simple model for actinide(IV) chemistry. In addition, we have selected a phosphorylated hexapeptide (His-pSer-Asp-Glu-pSer-Asp-Glu-Val) that is representative of the peptidic sequence involved in the bone interaction. For both the protein and the biomimetic peptide, we have determined the local environment of Th(IV) within the bioactinidic complex, combining isothermal titration calorimetry, attenuated total reflectance Fourier transform infrared spectroscopy, theoretical calculations with density functional theory, and extended X-ray absorption fine structure spectroscopy at the Th LIII edge. The results demonstrate a predominance of interaction of metal with the phosphate groups and confirmed the previous physiological studies that have highlighted a high affinity of Th(IV) for the bone matrix. Data are further compared with those of the uranyl case, representing the actinyl(V) and actinyl(VI) species. Last, our approach shows the importance of developing simplified systems [Th(IV)-peptide] that can serve as models for more biologically relevant systems.

  12. Stage IV work hardening in cubic metals

    SciTech Connect

    Rollett, A.D.; Kocks, U.F.; Doherty, R.D.

    1986-01-01

    The work hardening of fcc metals at large strains is discussed with reference to the linear stress-strain behavior often observed at large strains and known as Stage IV. The experimental evidence shows that Stage IV is a work hardening phenomenon that is found quite generally, even in pure fcc metals subjected to homogeneous deformation. A simple model for Stage IV in pure metals is presented, based on the accumulation of dislocation debris. Experiments are described for large strain torsion tests on four aluminum alloys. The level and extent of Stage IV scaled with the saturation stress that would represent the end of Stage III in the absence of a Stage IV. Reversing the torsion after large prestrains produced transient reductions in the work hardening. The strain rate sensitivity was also measured before and during the transient and found not to vary significantly. The microstructure observed at large strains in an Mg alloy suggest that Stage IV can occur in the absence of microband formation. Previous proposals for the cause of Stage IV are reviewed and found to be not supported by recent experimental data.

  13. High energy collimating fine grids

    NASA Technical Reports Server (NTRS)

    Arrieta, Victor M.; Tuffias, Robert H.; Laferla, Raffaele

    1995-01-01

    The objective of this project was to demonstrate the fabrication of extremely tight tolerance collimating grids using a high-Z material, specifically tungsten. The approach taken was to fabricate grids by a replication method involving the coating of a silicon grid substrate with tungsten by chemical vapor deposition (CVD). A negative of the desired grid structure was fabricated in silicon using highly wafering techniques developed for the semiconductor industry and capable of producing the required tolerances. Using diamond wafering blades, a network of accurately spaced slots was machined into a single-crystal silicon surface. These slots were then filled with tungsten by CVD, via the hydrogen reduction of tungsten hexafluoride. Following tungsten deposition, the silicon negative was etched away to leave the tungsten collimating grid structure. The project was divided into five tasks: (1) identify materials of construction for the replica and final collimating grid structures; (2) identify and implement a micromachining technique for manufacturing the negative collimator replicas (performed by NASA/JPL); (3) develop a CVD technique and processing parameters suitable for the complete tungsten densification of the collimator replicas; (4) develop a chemical etching technique for the removal of the collimator replicas after the tungsten deposition process; and (5) fabricate and deliver tungsten collimating grid specimens.

  14. High energy collimating fine grids

    NASA Astrophysics Data System (ADS)

    Arrieta, Victor M.; Tuffias, Robert H.; Laferla, Raffaele

    1995-02-01

    The objective of this project was to demonstrate the fabrication of extremely tight tolerance collimating grids using a high-Z material, specifically tungsten. The approach taken was to fabricate grids by a replication method involving the coating of a silicon grid substrate with tungsten by chemical vapor deposition (CVD). A negative of the desired grid structure was fabricated in silicon using highly wafering techniques developed for the semiconductor industry and capable of producing the required tolerances. Using diamond wafering blades, a network of accurately spaced slots was machined into a single-crystal silicon surface. These slots were then filled with tungsten by CVD, via the hydrogen reduction of tungsten hexafluoride. Following tungsten deposition, the silicon negative was etched away to leave the tungsten collimating grid structure. The project was divided into five tasks: (1) identify materials of construction for the replica and final collimating grid structures; (2) identify and implement a micromachining technique for manufacturing the negative collimator replicas (performed by NASA/JPL); (3) develop a CVD technique and processing parameters suitable for the complete tungsten densification of the collimator replicas; (4) develop a chemical etching technique for the removal of the collimator replicas after the tungsten deposition process; and (5) fabricate and deliver tungsten collimating grid specimens.

  15. SPECIFIC AND NON-SPECIFIC POLYSACCHARIDES OF TYPE IV PNEUMOCOCCUS

    PubMed Central

    Heidelberger, Michael; Kendall, Forrest E.

    1931-01-01

    1. Three nitrogen-containing polysaccharides have been isolated from autolyzed cultures of Type IV pneumococcus: (1) a type-specific carbohydrate differing markedly from those of Type I, II, and III pneumococcus, and representing a type of substance hitherto not observed among specific polysaccharides, (2) a chemically similar carbohydrate without specific function, and (3) the "C" substance, or species-specific polysaccharide of Tillett, Goebel, and Avery. 2. The chemical differences between the specific polysaccharides of Pneumococcus are discussed, and the relationship of the new examples to chitin is pointed out and its bearing indicated on the unsettled controversy as to whether or not chitin occurs in bacteria. 3. The data of Tillett, Goebel, and Avery on the "C" substance have been extended. PMID:19869869

  16. Coordination of tetravalent actinides (An = Th(IV), U(IV), Np(IV), Pu(IV)) with DOTA - from dimers to hexamers.

    PubMed

    Tamain, Christelle; Dumas, Thomas; Hennig, Christoph; Guilbaud, Philippe

    2017-03-10

    Three tetravalent actinide (An(IV)) hexanuclear clusters with the octahedral core [An6(OH)4O4]12+ (An(IV) = U(IV), Np(IV), Pu(IV)) were structurally characterized in solid state and in aqueous solution using single crystal X-ray diffraction, X-ray absorption, IR, Raman and UV-Visible spectroscopy. The observed structure, [An6(OH)4O4(H2O)8(HDOTA)4].HCl/HNO3.nH2O (An = U (I), Np (II), Pu (III)), consists of a An(IV) hexanuclear pseudo-octahedral cluster stabilized by DOTA (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid) ligands. The six actinide atoms are connected through alternative µ3-O2- and µ3-OH- groups. EXAFS investigations combined with UV-vis spectroscopy evidence the same local structure in moderate acidic and neutral aqueous solutions. The synthesis mechanism was partially elucidated and the main physicochemical properties (pH range stability, solubility and protonation constant) of the cluster were determined. The results underline the importance (i) to consider such polynuclear species in thermodynamic models and (ii) of competing reactions between hydrolysis and complexation. It is interesting to note that the same synthesis route with thorium(IV) leads to the formation of a dimer, Th2(H2O)10(H2DOTA)2.4NO3.xH2O (IV), which contrasts to the structure of the other An(IV) hexamers.

  17. Human fine body hair enhances ectoparasite detection.

    PubMed

    Dean, Isabelle; Siva-Jothy, Michael T

    2012-06-23

    Although we are relatively naked in comparison with other primates, the human body is covered in a layer of fine hair (vellus and terminal hair) at a relatively high follicular density. There are relatively few explanations for the evolutionary maintenance of this type of human hair. Here, we experimentally test the hypothesis that human fine body hair plays a defensive function against ectoparasites (bed bugs). Our results show that fine body hair enhances the detection of ectoparasites through the combined effects of (i) increasing the parasite's search time and (ii) enhancing its detection.

  18. Nanoscale Adhesion Forces of Pseudomonas aeruginosa Type IV Pili

    PubMed Central

    2015-01-01

    A variety of bacterial pathogens use nanoscale protein fibers called type IV pili to mediate cell adhesion, a primary step leading to infection. Currently, how these nanofibers respond to mechanical stimuli and how this response is used to control adhesion is poorly understood. Here, we use atomic force microscopy techniques to quantify the forces guiding the adhesion of Pseudomonas aeruginosa type IV pili to surfaces. Using chemical force microscopy and single-cell force spectroscopy, we show that pili strongly bind to hydrophobic surfaces in a time-dependent manner, while they weakly bind to hydrophilic surfaces. Individual nanofibers are capable of withstanding forces up to 250 pN, thereby explaining how they can resist mechanical stress. Pulling on individual pili yields constant force plateaus, presumably reflecting conformational changes, as well as nanospring properties that may help bacteria to withstand physiological shear forces. Analysis of mutant strains demonstrates that these mechanical responses originate solely from type IV pili, while flagella and the cell surface localized and proposed pili-associated adhesin PilY1 play no direct role. We also demonstrate that bacterial–host interactions involve constant force plateaus, the extension of bacterial pili, and the formation of membrane tethers from host cells. We postulate that the unique mechanical responses of type IV pili unravelled here enable the bacteria to firmly attach to biotic and abiotic surfaces and thus maintain attachment when subjected to high shear forces under physiological conditions, helping to explain why pili play a critical role in colonization of the host. PMID:25286300

  19. Group-IV midinfrared plasmonics

    NASA Astrophysics Data System (ADS)

    Biagioni, Paolo; Frigerio, Jacopo; Samarelli, Antonio; Gallacher, Kevin; Baldassarre, Leonetta; Sakat, Emilie; Calandrini, Eugenio; Millar, Ross W.; Giliberti, Valeria; Isella, Giovanni; Paul, Douglas J.; Ortolani, Michele

    2015-01-01

    The use of heavily doped semiconductors to achieve plasma frequencies in the mid-IR has been recently proposed as a promising way to obtain high-quality and tunable plasmonic materials. We introduce a plasmonic platform based on epitaxial n-type Ge grown on standard Si wafers by means of low-energy plasma-enhanced chemical vapor deposition. Due to the large carrier concentration achieved with P dopants and to the compatibility with the existing CMOS technology, SiGe plasmonics hold promises for mid-IR applications in optoelectronics, IR detection, sensing, and light harvesting. As a representative example, we show simulations of mid-IR plasmonic waveguides based on the experimentally retrieved dielectric constants of the grown materials.

  20. Fine-root responses to fertilization reveal multiple nutrient limitation in a lowland tropical forest.

    PubMed

    Wurzburger, Nina; Wright, S Joseph

    2015-08-01

    Questions remain as to which soil nutrients limit primary production in tropical forests. Phosphorus (P) has long been considered the primary limiting element in lowland forests, but recent evidence demonstrates substantial heterogeneity in response to nutrient addition, highlighting a need to understand and diagnose nutrient limitation across diverse forests. Fine-root characteristics including their abundance, functional traits, and mycorrhizal symbionts can be highly responsive to changes in soil nutrients and may help to diagnose nutrient limitation. Here, we document the response of fine roots to long-term nitrogen (N), P, and potassium (K) fertilization in a lowland forest in Panama. Because this experiment has demonstrated that N and K together limit tree growth and P limits fine litter production, we hypothesized that fine roots would also respond to nutrient addition. Specifically we hypothesized that N, P, and K addition would reduce the biomass, diameter, tissue density, and mycorrhizal colonization of fine roots, and increase nutrient concentration in root tissue. Most morphological root traits responded to the single addition of K and the paired addition of N and P, with the greatest response to all three nutrients combined. The addition of N, P, and K together reduced fine-root biomass, length, and tissue density, and increased specific root length, whereas root diameter remained unchanged. Nitrogen addition did not alter root N concentration, but P and K addition increased root P and K concentration, respectively. Mycorrhizal colonization of fine roots declined with N, increased with P, and was unresponsive to K addition. Although plant species composition remains unchanged after 14 years of fertilization, fine-root characteristics responded to N, P, and K addition, providing some of the strongest stand-level responses in this experiment. Multiple soil nutrients regulate fine-root abundance, morphological and chemical traits, and their association

  1. Site-specific ionisation edge fine-structure of Rutile in the electron microscope.

    PubMed

    Hetaba, Walid; Löffler, Stefan; Willinger, Marc-Georg; Schuster, Manfred Erwin; Schlögl, Robert; Schattschneider, Peter

    2014-08-01

    Combined Bloch-wave and density functional theory simulations are performed to investigate the effects of different channelling conditions on the fine-structure of electron energy-loss spectra. The simulated spectra compare well with experiments. Furthermore, we demonstrate that using this technique, the site-specific investigation of atomic orbitals is possible. This opens new possibilities for chemical analyses.

  2. CHARACTERIZATION OF FINE PARTICLE ASSOCIATED ORGANIC COMPOUNDS: INTERLABORATORY COMPARISON AND DEVELOPMENT OF STANDARD REFERENCE MATERIALS

    EPA Science Inventory

    Organic chemicals adsorbed to fine particulate matter (PM) in the ambient air account for a major component of the mass and include source tracers as well as toxic compounds that may contribute to adverse human health effects. The US EPA has established a PM 2.5 research progr...

  3. CHARACTERIZATION OF FINE PARTICLE ASSOCIATED ORGANIC COMPOUNDS: INTERLABORATORY COMPARISON AND DEVELOPMENT OF STANDARD REFERENCE MATERIALS

    EPA Science Inventory

    Organic chemicals adsorbed to fine particulate matter (PM) in the ambient air account for a major component of the mass and include source tracers as well as toxic compounds that may contribute to adverse human health effects. The US EPA has established a PM 2.5 research progr...

  4. DuPont Fined for Air Pollution at Deepwater, New Jersey

    EPA Pesticide Factsheets

    (New York, N.Y. - Jan. 8, 2015) - The U.S. Environmental Protection Agency announced today that E.I. DuPont de Nemours and Company (DuPont), has been fined $531,000 for alleged Clean Air Act violations at its chemical manufacturing plant in Deepwater, New

  5. Methyl ricinoleate as platform chemical for simultaneous production of fine chemicals and polymer precursors.

    PubMed

    Dupé, Antoine; Achard, Mathieu; Fischmeister, Cédric; Bruneau, Christian

    2012-11-01

    The modification of methyl ricinoleate by etherification of the hydroxyl group was accomplished by using a nonclassical ruthenium-catalyzed allylation reaction and also by esterification. Methyl ricinoleate derivatives were engaged in ring-closing metathesis (RCM) reactions leading to biosourced 3,6-dihydropyran and α,β-unsaturated lactone derivatives with concomitant production of polymer precursors. Sequential RCM/hydrogenation and RCM/cross-metathesis were also implemented as a straightforward method for the synthesis of tetrahydropyran and lactone derivatives as well as valuable monomers (i.e., polyamide precursors).

  6. Experimental Study of the Possibility to Make a Mortar with Ternary Sand (Natural and Artificial Fine Aggregates)

    NASA Astrophysics Data System (ADS)

    Baali, L.; Naceri, A.; Rahmouni, Z.; Mehidi, M. W. Noui

    This experimental study investigates the possibility to make a mortar with a ternary sand (natural and artificial fine aggregates). This method is utilized to correct the particle size distribution of various sands used in mortar. For this investigation, three sands have been used: a dune sand (DS), a slag sand (SS), and brick sand (BS) at different proportions in mortar. After crushing, the artificial fine aggregate (blast furnace slag and waste brick fine aggregate) was sifted in order to use it as fine aggregate. The effect of the quality and grain size distribution of natural fine aggregate (i.e., DS) and artificial fine aggregates (i.e., SS and BS) on the physical properties of ternary sand confected (density, porosity, fineness modulus, equivalent sand, particle size distribution, water absorption) and properties of fresh and hardened mortar were analysed. In the same way for this study, the physical properties and chemical compositions of DS, SS, BS and cement were investigated. The results obtained show that the mechanical strength on mortar depends of the nature and particle size distribution of sand studied. The reuse of this recycled material (slag blast furnace and waste brick) in the industry would contribute to the protection of the environment. This study shows the potential of this method to make mortar with ternary sand (natural and artificial fine aggreagates) in order to improve the physical properties of sand. Utilising natural and artificial fine aggregates to produce quality mortar should yield significant environmental benefits.

  7. DESIGN INFORMATION ON FINE PORE AERATION SYSTEMS

    EPA Science Inventory

    Field studies were conducted over several years at municipal wastewater treatment plants employing line pore diffused aeration systems. These studies were designed to produce reliable information on the performance and operational requirements of fine pore devices under process ...

  8. Immobilization of Rocky Flats Graphite Fines Residue

    SciTech Connect

    Rudisill, T.S.

    1999-04-06

    The development of the immobilization process for graphite fines has proceeded through a series of experimental programs. The experimental procedures and results from each series of experiments are discussed in this report.

  9. Ultrasound-Guided Fine Needle Aspiration Biopsy of the Thyroid

    MedlinePlus

    ... Index A-Z Ultrasound-Guided Fine Needle Aspiration Biopsy of the Thyroid An ultrasound-guided thyroid biopsy ... Thyroid? What is Ultrasound-Guided Fine Needle Aspiration Biopsy of the Thyroid? During a fine needle aspiration ...

  10. Identification of Novel Human Dipeptidyl Peptidase-IV Inhibitors of Natural Origin (Part II): In Silico Prediction in Antidiabetic Extracts

    PubMed Central

    Guasch, Laura; Sala, Esther; Ojeda, María José; Valls, Cristina; Bladé, Cinta; Mulero, Miquel; Blay, Mayte; Ardévol, Anna; Garcia-Vallvé, Santiago; Pujadas, Gerard

    2012-01-01

    Background Natural extracts play an important role in traditional medicines for the treatment of diabetes mellitus and are also an essential resource for new drug discovery. Dipeptidyl peptidase IV (DPP-IV) inhibitors are potential candidates for the treatment of type 2 diabetes mellitus, and the effectiveness of certain antidiabetic extracts of natural origin could be, at least partially, explained by the inhibition of DPP-IV. Methodology/Principal Findings Using an initial set of 29,779 natural products that are annotated with their natural source and an experimentally validated virtual screening procedure previously developed in our lab (Guasch et al.; 2012) [1], we have predicted 12 potential DPP-IV inhibitors from 12 different plant extracts that are known to have antidiabetic activity. Seven of these molecules are identical or similar to molecules with described antidiabetic activity (although their role as DPP-IV inhibitors has not been suggested as an explanation for their bioactivity). Therefore, it is plausible that these 12 molecules could be responsible, at least in part, for the antidiabetic activity of these extracts through their inhibitory effect on DPP-IV. In addition, we also identified as potential DPP-IV inhibitors 6 molecules from 6 different plants with no described antidiabetic activity but that share the same genus as plants with known antidiabetic properties. Moreover, none of the 18 molecules that we predicted as DPP-IV inhibitors exhibits chemical similarity with a group of 2,342 known DPP-IV inhibitors. Conclusions/Significance Our study identified 18 potential DPP-IV inhibitors in 18 different plant extracts (12 of these plants have known antidiabetic properties, whereas, for the remaining 6, antidiabetic activity has been reported for other plant species from the same genus). Moreover, none of the 18 molecules exhibits chemical similarity with a large group of known DPP-IV inhibitors. PMID:23028712

  11. Level III and IV Ecoregions by State

    EPA Pesticide Factsheets

    Information and links to downloadable maps and datasets for Level III and IV ecoregions, listed by state. Ecoregions are areas of general similarity in the type, quality, and quantity of environmental resources.

  12. Optimizing IV and V for Mature Organizations

    NASA Technical Reports Server (NTRS)

    Fuhman, Christopher

    2003-01-01

    NASA is intending for its future software development agencies to have at least a Level 3 rating in the Carnegie Mellon University Capability Maturity Model (CMM). The CMM has built-in Verification and Validation (V&V) processes that support higher software quality. Independent Verification and Validation (IV&V) of software developed by mature agencies can be therefore more effective than for software developed by less mature organizations. How is Independent V&V different with respect to the maturity of an organization? Knowing a priori the maturity of an organization's processes, how can IV&V planners better identify areas of need choose IV&V activities, etc? The objective of this research is to provide a complementary set of guidelines and criteria to assist the planning of IV&V activities on a project using a priori knowledge of the measurable levels of maturity of the organization developing the software.

  13. Optimizing IV and V for Mature Organizations

    NASA Technical Reports Server (NTRS)

    Fuhman, Christopher

    2003-01-01

    NASA is intending for its future software development agencies to have at least a Level 3 rating in the Carnegie Mellon University Capability Maturity Model (CMM). The CMM has built-in Verification and Validation (V&V) processes that support higher software quality. Independent Verification and Validation (IV&V) of software developed by mature agencies can be therefore more effective than for software developed by less mature organizations. How is Independent V&V different with respect to the maturity of an organization? Knowing a priori the maturity of an organization's processes, how can IV&V planners better identify areas of need choose IV&V activities, etc? The objective of this research is to provide a complementary set of guidelines and criteria to assist the planning of IV&V activities on a project using a priori knowledge of the measurable levels of maturity of the organization developing the software.

  14. IV&V Project Assessment Process Validation

    NASA Technical Reports Server (NTRS)

    Driskell, Stephen

    2012-01-01

    The Space Launch System (SLS) will launch NASA's Multi-Purpose Crew Vehicle (MPCV). This launch vehicle will provide American launch capability for human exploration and travelling beyond Earth orbit. SLS is designed to be flexible for crew or cargo missions. The first test flight is scheduled for December 2017. The SLS SRR/SDR provided insight into the project development life cycle. NASA IV&V ran the standard Risk Based Assessment and Portfolio Based Risk Assessment to identify analysis tasking for the SLS program. This presentation examines the SLS System Requirements Review/System Definition Review (SRR/SDR), IV&V findings for IV&V process validation correlation to/from the selected IV&V tasking and capabilities. It also provides a reusable IEEE 1012 scorecard for programmatic completeness across the software development life cycle.

  15. Effervescent Liquid Fine Mist Apparatus and Method

    DTIC Science & Technology

    2001-06-05

    SUBTITLE Effervescent Liquid Fine Mist Apparatus and Method 6. AUTHOR(S) Joseph E. Wolfe 7. PERFORMING ORGANIZATION NAME(S) AND ADDRESS(ES) Naval...chamber connected to the container; and at least one convergent/divergent nozzle connected to the mixing chamber. A method of forming an effervescent fine...mist, effervescent liquid mist 16. SECURITY CLASSIFICATION OF: unclassified a. REPORT Unclassified b. ABSTRACT Unclassified c. THIS PAGE

  16. Interaction of fine sediment with alluvial streambeds

    USGS Publications Warehouse

    Jobson, H.E.; Carey, W.P.

    1989-01-01

    An alluvial streambed can have a large capacity to store fine sediments that are extracted from the flow when instream concentrations are high and it can gradually release fine sediment to the flow when the instream concentrations are low. Several types of storage mechanisms are available depending on the relative size distribution of the suspended load and bed material, as well as the flow hydraulics. -from Authors

  17. NUMERICAL MODELING OF FINE SEDIMENT PHYSICAL PROCESSES.

    USGS Publications Warehouse

    Schoellhamer, David H.

    1985-01-01

    Fine sediment in channels, rivers, estuaries, and coastal waters undergo several physical processes including flocculation, floc disruption, deposition, bed consolidation, and resuspension. This paper presents a conceptual model and reviews mathematical models of these physical processes. Several general fine sediment models that simulate some of these processes are reviewed. These general models do not directly simulate flocculation and floc disruption, but the conceptual model and existing functions are shown to adequately model these two processes for one set of laboratory data.

  18. Analysis of Diffraction Anomalous Fine Structure

    NASA Astrophysics Data System (ADS)

    Cross, Julie Olmsted

    This thesis presents a systematic study of the application of DAFS to determine site-specific local structural and chemical information in complex materials, and the first application of state-of-the-art theoretical XAFS calculations using the computer program scFEFF to model DAFS data. In addition, the iterative dispersion analysis method, first suggested by Pickering, et al., has been generalized to accommodate the off-resonance anomalous scattering from heavy atoms in the unit cell. The generalized algorithm scKKFIT was applied to DAFS data from eight (00 l) reflections of the high-T _{c} superconductor YBa _2Cu_3O_ {6.8} to obtain the weighted complex resonant scattering amplitudes Delta f_{ rm w}(Q, E). The fine-structure functions chi_{rm w}(Q, E) isolated from the Delta f_{ rm w}(Q, E) are linear combinations of the individual site fine structure functions chi _{rm w}(Q, E) = Sigma_{i}W_{i,{ bf Q}}chi_{i}(E) from the two inequivalent Cu sites, added together according to the structure factor for the Cu sublattice. The chi_{rm w}(Q, E) were fit en masse using the XAFS analysis program scFEFFIT under a set of constraints on the coefficients W _{i,{bf Q}} based on the structure factor for kinematic scattering. The W_{i,{bf Q}} determined by scFEFFIT were used to obtain the fully separated complex resonant scattering amplitudes Delta f(E) for the two Cu sites. The theoretical connection between DAFS and XAFS is used to justify the application of state-of-the-art theoretical XAFS calculations to DAFS analysis. The polarization dependence of DAFS is described in terms of individual virtual photoelectron scattering paths in the Rehr-Albers separable curved-wave formalism. Polarization is shown to be an important factor in all DAFS experiments. Three experimental constraints are found necessary for obtaining site-separated Delta f(E) from DAFS data by linear inversion of the W_{i, {bf Q}} matrix and scKKFIT isolated Delta f_{rm w }(Q, E): (1) The diffraction must be

  19. Lunar regolith fines - A source of hydrogen

    NASA Technical Reports Server (NTRS)

    Carter, J. L.

    1985-01-01

    The theoretical evaluation of the lunar regolith fines as a primary source of hydrogen reveals that a minimum order of magnitude increase in hydrogen content is possible in beneficiated fines because both particle size and particle shape play a significant role in the relationship of volume percent of surface coating to grain size. The lunar regolith fines meet the basic requirement for beneficiation because a major portion (minimum two-thirds) of the hydrogen occurs in the less than 20-micron-size fraction, a relatively small part of the fines. Beneficiation should be accomplished by a combination of vibratory screening followed by cyclone and/or possibly electrostatic separation. Early exploitation of the lunar regolith fines for hydrogen probably will be limited to hydrogen obtained as a by-product or co-product from the mining and processing for other elements or materials because a minimum of about 13,600 tons to about 19,600 tons of 100 ppm hydrogen-bearing lunar regolith fines will have to be processed with about 3,100 tons to about 4,500 tons, respectively, of concentrate heated to supply 1 ton of hydrogen, yielding a recovery of about 74 percent to about 51 percent respectively, of the hydrogen.

  20. Revisiting fine-tuning in the MSSM

    NASA Astrophysics Data System (ADS)

    Ross, Graham G.; Schmidt-Hoberg, Kai; Staub, Florian

    2017-03-01

    We evaluate the amount of fine-tuning in constrained versions of the minimal supersymmetric standard model (MSSM), with different boundary conditions at the GUT scale. Specifically we study the fully constrained version as well as the cases of non-universal Higgs and gaugino masses. We allow for the presence of additional non-holomorphic soft-terms which we show further relax the fine-tuning. Of particular importance is the possibility of a Higgsino mass term and we discuss possible origins for such a term in UV complete models. We point out that loop corrections typically lead to a reduction in the fine-tuning by a factor of about two compared to the estimate at tree-level, which has been overlooked in many recent works. Taking these loop corrections into account, we discuss the impact of current limits from SUSY searches and dark matter on the fine-tuning. Contrary to common lore, we find that the MSSM fine-tuning can be as small as 10 while remaining consistent with all experimental constraints. If, in addition, the dark matter abundance is fully explained by the neutralino LSP, the fine-tuning can still be as low as ˜ 20 in the presence of additional non-holomorphic soft-terms. We also discuss future prospects of these models and find that the MSSM will remain natural even in the case of a non-discovery in the foreseeable future.

  1. Observational properties of decameter type IV bursts

    NASA Astrophysics Data System (ADS)

    Melnik, Valentin; Brazhenko, Anatoly; Rucker, Helmut; Konovalenko, Alexander; Briand, Carine; Dorovskyy, Vladimir; Zarka, Philippe; Frantzusenko, Anatoly; Panchenko, Michael; Poedts, Stefan; Zaqarashvili, Teimuraz; Shergelashvili, Bidzina

    2013-04-01

    Oscillations of decameter type IV bursts were registered during observations of solar radio emission by UTR-2, URAN-2 and NDA in 2011-2012. Large majority of these bursts were accompanied by coronal mass ejections (CMEs), which were observed by SOHO and STEREO in the visible light. Only in some cases decameter type IV bursts were not associated with CMEs. The largest periods of oscillations P were some tens of minutes. There were some modes of long periods of oscillations simultaneously. Periods of oscillations in flux and in polarization profiles were close. Detailed properties of oscillations at different frequencies were analyzed on the example of two type IV bursts. One of them was observed on April 7, 2011 when a CME happened. Another one (August 1, 2011) was registered without any CME. The 7 April type IV burst had two periods in the frames 75-85 and 35-85 minutes. Interesting feature of these oscillations is decreasing periods with time. The observed decreasing rates dP/dt equaled 0.03-0.07. Concerning type IV burst observed on August 1, 2011 the period of its oscillations increases from 17 min. at 30 MHz to 44 min. at 10 MHz. Connection of type IV burst oscillations with oscillations of magnetic arches and CMEs at corresponding altitudes are discussed. The work is fulfilled in the frame of FP7 project "SOLSPANET".

  2. Reaction of U(VI) with titanium-substituted magnetite: influence of Ti on U(IV) speciation.

    PubMed

    Latta, Drew E; Pearce, Carolyn I; Rosso, Kevin M; Kemner, Kenneth M; Boyanov, Maxim I

    2013-05-07

    Reduction of hexavalent uranium (U(VI)) to less soluble tetravalent uranium (U(IV)) through enzymatic or abiotic redox reactions has the potential to alter U mobility in subsurface environments. As a ubiquitous natural mineral, magnetite (Fe3O4) is of interest because of its ability to act as a rechargeable reductant for U(VI). Natural magnetites are often impure with titanium, and structural Fe(3+) replacement by Ti(IV) yields a proportional increase in the relative Fe(2+) content in the metal sublattice to maintain bulk charge neutrality. In the absence of oxidation, the Ti content sets the initial bulk Fe(2+)/Fe(3+) ratio (R). Here, we demonstrate that Ti-doped magnetites (Fe3 - xTixO4) reduce U(VI) to U(IV). The U(VI)-Fe(2+) redox reactivity was found to be controlled directly by R but was otherwise independent of Ti content (xTi). However, in contrast to previous studies with pure magnetite where U(VI) was reduced to nanocrystalline uraninite (UO2), the presence of structural Ti (xTi = 0.25-0.53) results in the formation of U(IV) species that lack the bidentate U-O2-U bridges of uraninite. Extended X-ray absorption fine structure spectroscopic analysis indicated that the titanomagnetite-bound U(IV) phase has a novel U(IV)-Ti binding geometry different from the coordination of U(IV) in the mineral brannerite (U(IV)Ti2O6). The observed U(IV)-Ti coordination at a distance of 3.43 Å suggests a binuclear corner-sharing adsorption/incorporation U(IV) complex with the solid phase. Furthermore, we explored the effect of oxidation (decreasing R) and solids-to-solution ratio on the reduced U(IV) phase. The formation of the non-uraninite U(IV)-Ti phase appears to be controlled by availability of surface Ti sites rather than R. Our work highlights a previously unrecognized role of Ti in the environmental chemistry of U(IV) and suggests that further work to characterize the long-term stability of U(IV) phases formed in the presence of Ti is warranted.

  3. The protonation states of oxo-bridged Mn(IV) dimers resolved by experimental and computational Mn K pre-edge X-ray absorption spectroscopy.

    PubMed

    Krewald, Vera; Lassalle-Kaiser, Benedikt; Boron, Thaddeus T; Pollock, Christopher J; Kern, Jan; Beckwith, Martha A; Yachandra, Vittal K; Pecoraro, Vincent L; Yano, Junko; Neese, Frank; DeBeer, Serena

    2013-11-18

    In nature, the protonation of oxo bridges is a commonly encountered mechanism for fine-tuning chemical properties and reaction pathways. Often, however, the protonation states are difficult to establish experimentally. This is of particular importance in the oxygen evolving complex of photosystem II, where identification of the bridging oxo protonation states is one of the essential requirements toward unraveling the mechanism. In order to establish a combined experimental and theoretical protocol for the determination of protonation states, we have systematically investigated a series of Mn model complexes by Mn K pre-edge X-ray absorption spectroscopy. An ideal test case for selective bis-μ-oxo-bridge protonation in a Mn dimer is represented by the system [Mn(IV)2(salpn)2(μ-OHn)2](n+). Although the three species [Mn(IV)2(salpn)2(μ-O)2], [Mn(IV)2(salpn)2(μ-O)(μ-OH)](+) and [Mn(IV)2(salpn)2(μ-OH)2](2+) differ only in the protonation of the oxo bridges, they exhibit distinct differences in the pre-edge region while maintaining the same edge energy. The experimental spectra are correlated in detail to theoretically calculated spectra. A time-dependent density functional theory approach for calculating the pre-edge spectra of molecules with multiple metal centers is presented, using both high spin (HS) and broken symmetry (BS) electronic structure solutions. The most intense pre-edge transitions correspond to an excitation of the Mn 1s core electrons into the unoccupied orbitals of local e(g) character (d(z)(2) and d(xy) based in the chosen coordinate system). The lowest energy experimental feature is dominated by excitations of 1s-α electrons, and the second observed feature is primarily attributed to 1s-β electron excitations. The observed energetic separation is due to spin polarization effects in spin-unrestricted density functional theory and models final state multiplet effects. The effects of spin polarization on the calculated Mn K pre-edge spectra, in

  4. Chemical Peel

    MedlinePlus

    ... be done at different depths — light, medium or deep — depending on your desired results. Each type of ... chemical peel after 12 months to maintain results. Deep chemical peel. A deep chemical peel removes skin ...

  5. Process for recovering fine coal particles from slurry of finely divided coal

    SciTech Connect

    Harada, K.; Ogino, E.; Yoshii, N.

    1982-08-24

    Fine coal particles are recovered from a slurry of finely divided coal by mixing coarsely divided coal and a binder together to cause the binder to adhere to the surfaces of the coarsely divided coal pieces, mixing the slurry with the coal pieces having the binder adhered thereto to cause fine coal particles to adhere to the binder over the surfaces of the coal pieces serving as nuclei and thereby form agglomerates, and separating the agglomerates from the remaining slurry portion to recover the fine coal particles along with the coarsely divided coal and the binder.

  6. Emissions of fine particle fluoride from biomass burning.

    PubMed

    Jayarathne, Thilina; Stockwell, Chelsea E; Yokelson, Robert J; Nakao, Shunsuke; Stone, Elizabeth A

    2014-11-04

    The burning of biomasses releases fluorine to the atmosphere, representing a major and previously uncharacterized flux of this atmospheric pollutant. Emissions of fine particle (PM2.5) water-soluble fluoride (F-) from biomass burning were evaluated during the fourth Fire Laboratory at Missoula Experiment (FLAME-IV) using scanning electron microscopy energy dispersive X-ray spectroscopy (SEM-EDX) and ion chromatography with conductivity detection. F- was detected in 100% of the PM2.5 emissions from conifers (n=11), 94% of emissions from agricultural residues (n=16), and 36% of the grasses and other perennial plants (n=14). When F- was quantified, it accounted for an average (±standard error) of 0.13±0.02% of PM2.5. F- was not detected in remaining samples (n=15) collected from peat burning, shredded tire combustion, and cook-stove emissions. Emission factors (EF) of F- emitted per kilogram of biomass burned correlated with emissions of PM2.5 and combustion efficiency, and also varied with the type of biomass burned and the geographic location where it was harvested. Based on recent evaluations of global biomass burning, we estimate that biomass burning releases 76 Gg F- yr(-1) to the atmosphere, with upper and lower bounds of 40-150 Gg F- yr(-1). The estimated F- flux from biomass burning is comparable to total fluorine emissions from coal combustion plus other anthropogenic sources. These data demonstrate that biomass burning represents a major source of fluorine to the atmosphere in the form of fine particles, which have potential to undergo long-range transport.

  7. A Global Perspective of Fine Particulate Matter Pollution and Its Health Effects.

    PubMed

    Mukherjee, Arideep; Agrawal, Madhoolika

    2017-03-31

    Fine particulate matter (PM) in the ambient air is implicated in a variety of human health issues throughout the globe. Regulation of fine PM in the atmosphere requires information on the dimension of the problem with respect to variations in concentrations and sources. To understand the current status of fine particles in the atmosphere and their potential harmful health effects in different regions of the world this review article was prepared based on peer-reviewed scientific papers, scientific reports, and database from government organizations published after the year 2000 to evaluate the global scenario of the PM2.5 (particles <2.5 μm in aerodynamic diameter), its exceedance of national and international standards, sources, mechanism of toxicity, and harmful health effects of PM2.5 and its components. PM2.5 levels and exceedances of national and international standards were several times higher in Asian countries, while levels in Europe and USA were mostly well below the respective standards. Vehicular traffic has a significant influence on PM2.5 levels in urban areas; followed by combustion activities (biomass, industrial, and waste burning) and road dust. In urban atmosphere, fine particles are mostly associated with different health effects with old aged people, pregnant women, and more so children being the most susceptible ones. Fine PM chemical constituents severely effect health due to their carcinogenic or mutagenic nature. Most of the research indicated an exceedance of fine PM level of the standards with a diverse array of health effects based on PM2.5 chemical constituents. Emission reduction policies with epidemiological studies are needed to understand the benefits of sustainable control measures for fine PM mitigation.

  8. Fine Shades of a Sombrero

    NASA Astrophysics Data System (ADS)

    2000-02-01

    In addition to their scientific value, many of the exposures now being obtained by visiting astronomers to ESO's Very Large Telescope (VLT) are also very beautiful. This is certainly true for this new image of the famous early-type spiral galaxy Messier 104 , widely known as the "Sombrero" (the Mexican hat) because of its particular shape. The colour image was made by a combination of three CCD images from the FORS1 multi-mode instrument on VLT ANTU , recently obtained by Peter Barthel from the Kapteyn Institute (Groningen, The Netherlands) during an observing run at the Paranal Observatory. He and Mark Neeser , also from the Kapteyn Institute, produced the composite images. The galaxy fits perfectly into the 6.8 x 6.8 arcmin 2 field-of-view of the FORS1 camera. A great amount of fine detail is revealed, from the structures in the pronounced dust band in the equatorial plane, to many faint background galaxies that shine through the outer regions. The "Sombrero" is located in the constellation Virgo (The Virgin), at a distance of about 50 million light-years. The overall "sharpness" of this colour image corresponds to about 0.7 arcsec which translates into a resolution of about 170 light-years at that distance. About Messier 104 Messier 104 is the 104th object in the famous catalogue of nebulae by French astronomer Charles Messier (1730 - 1817). It was not included in the first two editions (with 45 objects in 1774; 103 in 1781), but Messier soon thereafter added it by hand in his personal copy as a "very faint nebula". The recession velocity, about 1000 km/sec, was first measured by American astronomer Vesto M. Slipher at the Lowell Observatory in 1912; he was also the first to detect the galaxy's rotation. ESO Press Photo 07c/00 ESO Press Photo 07c/00 [Preview; JPEG: 400 x 307; 59k] [Normal; JPEG: 800 x 614; 308k] [Full-Res; JPEG: 2028 x 1556; 2.3Mb] PR Photo 07c/00 has been processed to show the numerous dust bands in the central plane of the Sombrero galaxy (see

  9. Water transfer between rock fragments and fine earth in remoulded soils

    NASA Astrophysics Data System (ADS)

    Tetegan, Marion; Korboulewsky, Nathalie; Bouthier, Alain; Cousin, Isabelle

    2010-05-01

    Stony soils cover about 30% of the surface soils of Western Europe, and 60% in Mediterranean areas. Rock fragments may alter the physical, chemical and agricultural properties of soils. They are also a potential reservoir of water and nutrients for plants, suggesting that the stony phase of soil can participate in water supply to crops and affect the storage capacity of soil water. This implies the existence of water transfer between rock fragments and fine earth. To better understand the interaction between the fine earth and rock fragments, we studied the water transfer between pebbles and fine earth on remoulded soils in presence and absence of plants. Experiments were conducted on remoulded soils in containers (3 L), under controlled conditions. Pebbles and fine earth were collected separately from the Ap horizon of a calcareous lacustrine limestone silty soil located in the central region of France. Pebbles were mixed with fine earth to reach a bulk density of the fine earth of 1.1 g/cm3. Four modalities with different percentage in volume of pebbles were created: 0%p: 0 % pebbles + 100 % fine earth + plant 20%p: 20 % pebbles + 80% fine earth + plant 40%p: 40 % pebbles + 60% fine earth + plant 40%: 40 % pebbles + 60% fine earth Fifteen containers were created for each modality and cuttings of Populus robusta were planted in the three first modalities. All containers were saturated, then irrigated by capillarity and controlled to maintain a moderate water stress continuously. After three months, the containers were saturated again and then allowed to dry. At that time, plants were from 27 to 43 cm height depending on the modality. Soil samples were collected at 5 dates following this second saturation: D0 = soil water content equal to the Available Water Content, Day 2 = D0 + 2 days, Day 4 = D0 + 4 days, Day 7 = D0 + 7 days, Day 11= D0 + 11 days. At each sampling date, three containers for each modality were used to measure the gravimetric water content

  10. Uptake of Np(IV) by C-S-H phases and cement paste: an EXAFS study.

    PubMed

    Gaona, Xavier; Dähn, Rainer; Tits, Jan; Scheinost, Andreas C; Wieland, Erich

    2011-10-15

    Nuclear waste disposal concepts developed worldwide foresee the use of cementitious materials for the immobilization of long-lived intermediate level waste (ILW). This waste form may contain significant amounts of neptunium-237, which is expected to be present as Np(IV) under the reducing conditions encountered after the closure of the repository. Predicting the release of Np(IV) from the cementitious near field of an ILW repository requires a sufficiently detailed understanding of its interaction with the main sorbing components of hardened cement paste (HCP). In this study, the uptake of Np(IV) by calcium silicate hydrates (C-S-H) and HCP has been investigated using extended X-ray absorption fine structure (EXAFS) spectroscopy. The EXAFS studies on Np(IV)-doped C-S-H and HCP samples reveal that Np(IV) is predominantly incorporated in the structure of C-S-H phases having different Ca:Si ratios. The two main species identified correspond to Np(IV) in C-S-H with a Ca:Si mol ratio of 1.65 as in fresh cement and with a Ca:Si mol ratio of 0.75 as in highly degraded cement. The local structure of Np(IV) changes with the Ca:Si mol ratio and does not depend on pH. Furthermore, Np(IV) shows the same coordination environment in C-S-H and HCP samples. This study shows that C-S-H phases are responsible for the Np(IV) uptake by cementitious materials and further that incorporation in the interlayer of the C-S-H structure is the dominant uptake mechanism.

  11. Observation of step structures in the I-V characteristics of YBCO thin films

    NASA Astrophysics Data System (ADS)

    Azoulay, J.; Verdyan, A.; Lapsker, I.

    1997-08-01

    Many electrical properties of the high Tc superconductors are widely probed utilizing current-voltage characteristics because of its sensitivity to the phase transition. In this work we report on detailed study of YBCO I-V characteristics shape above the critical current in the phase transition vicinity. For a given temperature controlled to a better than 10mK stability over the whole I-V cycle, the applied current has been gradually increased to exceed the critical current. The system has thus been driven to cross over to the mixed state. Using dI/dV versus V plots, it is shown that all the curves are characterized by a fine step structures at current densities higher than the critical ones.

  12. Main ethanol metabolizing alcohol dehydrogenases (ADH I and ADH IV): biochemical functions and the physiological manifestation.

    PubMed

    Ashmarin, I P; Danilova, R A; Obukhova, M F; Moskvitina, T A; Prosorovsky, V N

    2000-12-01

    The range of the biochemical reactions which can be catalyzed by ADH I and ADH IV is extremely wide. The most characterized functions of these enzymes are protection against excess endogenous acetaldehyde, products of lipid peroxidation, exogenous alcohols and some xenobiotics. It was found also that ADH I and ADH IV are important members of the enzyme system synthesizing retinoic acid (especially during embryogenesis). They can oxidize some steroids and participate in bioamine and prostaglandin metabolism but so far the extent of their contribution to the latter processes is under discussion. Recent data suggest a correlation between the activity of ADH I in some organs and fine physiological processes including behavior regulation and craving for alcohol in albino rats.

  13. Irradiation effects in oxide dispersion strengthened (ODS) Ni-base alloys for Gen. IV nuclear reactors

    NASA Astrophysics Data System (ADS)

    Oono, Naoko; Ukai, Shigeharu; Kondo, Sosuke; Hashitomi, Okinobu; Kimura, Akihiko

    2015-10-01

    Oxide particle dispersion strengthened (ODS) Ni-base alloys are irradiated by using simulation technique (Fe/He dual-ion irradiation) to investigate the reliability to Gen. IV high-temperature reactors. The fine oxide particles with less than 10 nm in average size and approximately 8.0 × 1022 m-3 in number density remained after 101 dpa irradiation. The tiny helium bubbles were inside grains, not at grain-boundaries; it is advantageous effect of oxide particles which trap the helium atoms at the particle-matrix interface. Ni-base ODS alloys demonstrated their great ability to overcome He embrittlement.

  14. Complexation Behavior of the Tri-n-butyl Phosphate Ligand with Pu(IV) and Zr(IV): A Computational Study.

    PubMed

    Gopakumar, Gopinadhanpillai; Sreenivasulu, B; Suresh, A; Brahmmananda Rao, C V S; Sivaraman, N; Joseph, M; Anoop, Anakuthil

    2016-06-23

    Tri-n-butyl phosphate (TBP), used as the extractant in nuclear fuel reprocessing, shows superior extraction abilities for Pu(IV) over a large number of fission products including Zr(IV). We have applied density functional theory (DFT) calculations to explain this selectivity by investigating differences in electronic structures of Pu(NO3)4·2TBP and Zr(NO3)4·2TBP complexes. On the basis of our quantum chemical calculations, we have established the lowest energy electronic states for both complexes; the quintet is the ground state for the former, whereas the latter exists in the singlet spin state. The calculated structural parameters for the optimized geometry of the plutonium complex are in agreement with the experimental results. Atoms in Molecules analysis revealed a considerable amount of ionic character to M-O{TBP} and M-O{NO3} bonds. Additionally, we have also investigated the extraction behavior of TBP for metal nitrates and have estimated the extraction energies to be -73.1 and -57.6 kcal/mol for Pu(IV) and Zr(IV), respectively. The large extraction energy of Pu(IV) system is in agreement with the observed selectivity in the extraction of Pu.

  15. Relative Reactivity of Biogenic and Chemogenic Uraninite and Biogenic Non Crystalline U(IV)

    PubMed Central

    Cerrato, José M.; Ashner, Matthew N.; Alessi, Daniel S.; Lezama-Pacheco, Juan S.; Bernier-Latmani, Rizlan; Bargar, John R.; Giammar, Daniel E.

    2013-01-01

    Aqueous chemical extractions and X-ray absorption spectroscopy (XAS) analyses were conducted to investigate the reactivity of chemogenic uraninite, nanoparticulate biogenic uraninite, and biogenic monomeric U(IV) species. The analyses were conducted in systems containing a total U concentration that ranged from 1.48 to 2.10 mM. Less than 0.02% of the total U was released to solution in extractions that targeted water soluble and ion exchangeable fractions. Less than 5% of the total U was solubilized via complexation with a 0.1 M solution of NaF. Greater than 90% of the total U was extracted from biogenic uraninite and monomeric U(IV) after 6 hours of reaction in an oxidizing solution of 50 mM K2S2O8. Additional oxidation experiments with lower concentrations (2 mM and 10 mM) of K2S2O8 and 8.2 mg L−1 dissolved oxygen suggested that monomeric U(IV) species are more labile than biogenic uraninite; chemogenic uraninite was much less susceptible to oxidation than either form of biogenic U(IV). These results suggest that non-crystalline forms of U(IV) may be more labile than uraninite in subsurface environments. This work helps fill critical gaps in our understanding of the behavior of solid-associated U(IV) species in bioremediated sites and natural uranium ore deposits. PMID:23906226

  16. Experimental and Computational Evidence of the Biradical Structure and Reactivity of Titanium(IV) Enolates.

    PubMed

    Heras, Carlos; Gómez-Palomino, Alejandro; Romea, Pedro; Urpí, Fèlix; Bofill, Josep Maria; Moreira, Ibério de P R

    2017-09-01

    Quantum chemical calculations have unveiled the unexpected biradical character of titanium(IV) enolates from N-acyl oxazolidinones and thiazolidinethiones. The electronic structure of these species therefore involves a valence tautomerism consisting of an equilibrium between a closed shell (formally Ti(IV) enolates) and an open shell, biradical, singlet (formally Ti(III) enolates) electronic states, whose origin is to be basically found in changes of the Ti-O distance. Spectroscopic studies of the intermediate species lend support to such a model, which also turns out to be crucial for a better understanding of the overall reactivity of titanium(IV) enolates. In this context, a thorough computational analysis of the radical addition of titanium(IV) enolates from N-acyl oxazolidinones to TEMPO has permitted us to suggest an entire mechanism, which accounts for the experimental details and the diastereoselectivity of the process. All together, this evidence highlights the relevance of biradical intermediates from titanium(IV) enolates and may be a useful contribution to the foundations of a more insightful comprehension of the structure and reactivity of titanium(IV) enolates.

  17. Estimation of Se(VI)/Se(IV) ratio in water by the ratio recorded in barite

    NASA Astrophysics Data System (ADS)

    Tokunaga, Kohei; Yokoyama, Yuka; Takahashi, Yoshio

    2013-11-01

    It is possible that the distribution behaviors of redox-sensitive elements such as selenium (Se) between authigenic minerals and water can provide information on the oxidation state of the element in the coexistent water during mineral deposition. Considering the similar chemical characteristics of Se(IV) and Se(VI) oxyanions, we propose that the Se(VI)/Se(IV) ratio in a particular precipitate, such as barite, may enable us to estimate the Se(VI)/Se(IV) ratio in the coexistent water. The coprecipitation experiments of Se with barite coupled with the determination of the oxidation state of Se both in the aqueous phase and in barite were conducted by Se K-edge X-ray absorption near-edge structure and high-performance liquid chromatography connected to inductively coupled plasma-mass spectrometry, respectively, to investigate the influence of the oxidation state of Se on its immobilization into barite at pH 4.0 and 8.0. The results showed that the Se(VI)/Se(IV) ratio in barite was correlated with the Se(VI)/Se(IV) ratio in water, which in turn can provide physicochemical and biogeochemical information related to the Se(VI)/Se(IV) ratio in water in the environment where barite precipitated.

  18. Analysis of vegetable seedlings grown in contact with Apollo 14 lunar surface fines.

    NASA Technical Reports Server (NTRS)

    Walkinshaw, C. H.; Johnson, P. H.

    1971-01-01

    Study of plant seedlings treated with lunar material, grown for 14 to 21 days, and then subjected to chemical analyses and other measurements. The purpose of the study was to determine whether plants growing in contact with lunar-surface fines contained a different elemental composition compared with untreated seedlings. The results indicate a direct interaction between germfree plants and lunar material. Treated plants dissolved and absorbed significant quantities of Al, Fe, and Ti from the lunar fines. Cabbage and Brussel sprouts were particularly efficient in the dissolution and absorption of Mn.

  19. Origin of zoned fine-grained inclusions in the Allende meteorite

    NASA Technical Reports Server (NTRS)

    Mcgurie, Anne V.; Hashimoto, Akihiko

    1989-01-01

    The mineral and bulk compositions in the three zones of the fine-grained Ca-Al-rich inclusion in the Allende meteorite are studied. Mineral analyses for the inclusions are presented and the principle mineral composition for the three zones of the inclusions are described. The nature of the alteration and the physical and chemical environment which caused the three-fold zonation are examined. An alteration and origin of zonation for the Allende inclusions are proposed. It is noted that the fine-grained inclusions display alteration processes such as Ca-Fe-silicate condensation and characteristics of the primary inclusion such as different rim type.

  20. Analysis of vegetable seedlings grown in contact with Apollo 14 lunar surface fines.

    NASA Technical Reports Server (NTRS)

    Walkinshaw, C. H.; Johnson, P. H.

    1971-01-01

    Study of plant seedlings treated with lunar material, grown for 14 to 21 days, and then subjected to chemical analyses and other measurements. The purpose of the study was to determine whether plants growing in contact with lunar-surface fines contained a different elemental composition compared with untreated seedlings. The results indicate a direct interaction between germfree plants and lunar material. Treated plants dissolved and absorbed significant quantities of Al, Fe, and Ti from the lunar fines. Cabbage and Brussel sprouts were particularly efficient in the dissolution and absorption of Mn.