Science.gov

Sample records for acidic salts deposits

  1. Nitric Acid-Sea Salt Reactions: Implications for Nitrogen Deposition to Water Surfaces.

    NASA Astrophysics Data System (ADS)

    Pryor, S. C.; Sørensen, L. L.

    2000-05-01

    Many previous studies have indicated the importance of nitric acid (HNO3) reactions on sea salt particles for flux divergence of HNO3 in the marine surface layer. The potential importance of this reaction in determining the spatial and temporal patterns of nitrogen dry deposition to marine ecosystems is investigated using models of sea spray generation and particle- and gas-phase dry deposition. Under horizontally homogeneous conditions with near-neutral stability and for wind speeds between 3.5 and 10 m s1, transfer of HNO3 to the particle phase to form sodium nitrate may decrease the deposition velocity of nitrogen by over 50%, leading to greater horizontal transport prior to deposition to the sea surface. Conversely, for wind speeds above 10 m s1, transfer of nitrogen to the particle phase would increase the deposition rate and hence decrease horizontal transport prior to surface removal.

  2. Acid Deposition

    EPA Science Inventory

    This indicator presents acid deposition trends in the contiguous U.S. from 1989 to 2007. Data are broken down by wet and dry deposition and deposition of nitrogen and sulfur compounds. Acid deposition is particularly damaging to lakes, streams, and forests and the plants and a...

  3. Hydroxycarboxylic acids and salts

    DOEpatents

    Kiely, Donald E; Hash, Kirk R; Kramer-Presta, Kylie; Smith, Tyler N

    2015-02-24

    Compositions which inhibit corrosion and alter the physical properties of concrete (admixtures) are prepared from salt mixtures of hydroxycarboxylic acids, carboxylic acids, and nitric acid. The salt mixtures are prepared by neutralizing acid product mixtures from the oxidation of polyols using nitric acid and oxygen as the oxidizing agents. Nitric acid is removed from the hydroxycarboxylic acids by evaporation and diffusion dialysis.

  4. A global assessment of precipitation chemistry and deposition of sulfur, nitrogen, sea salt, base cations, organic acids, acidity and pH, and phosphorus

    NASA Astrophysics Data System (ADS)

    Vet, Robert; Artz, Richard S.; Carou, Silvina; Shaw, Mike; Ro, Chul-Un; Aas, Wenche; Baker, Alex; Bowersox, Van C.; Dentener, Frank; Galy-Lacaux, Corinne; Hou, Amy; Pienaar, Jacobus J.; Gillett, Robert; Forti, M. Cristina; Gromov, Sergey; Hara, Hiroshi; Khodzher, Tamara; Mahowald, Natalie M.; Nickovic, Slobodan; Rao, P. S. P.; Reid, Neville W.

    2014-08-01

    A global assessment of precipitation chemistry and deposition has been carried out under the direction of the World Meteorological Organization (WMO) Global Atmosphere Watch (GAW) Scientific Advisory Group for Precipitation Chemistry (SAG-PC). The assessment addressed three questions: (1) what do measurements and model estimates of precipitation chemistry and wet, dry and total deposition of sulfur, nitrogen, sea salt, base cations, organic acids, acidity, and phosphorus show globally and regionally? (2) has the wet deposition of major ions changed since 2000 (and, where information and data are available, since 1990) and (3) what are the major gaps and uncertainties in our knowledge? To that end, regionally-representative measurements for two 3-year-averaging periods, 2000-2002 and 2005-2007, were compiled worldwide. Data from the 2000-2002 averaging period were combined with 2001 ensemble-mean modeling results from 21 global chemical transport models produced in Phase 1 of the Coordinated Model Studies Activities of the Task Force on Hemispheric Transport of Air Pollution (TF HTAP). The measurement data and modeling results were used to generate global and regional maps of major ion concentrations in precipitation and deposition. A major product of the assessment is a database of quality assured ion concentration and wet deposition data gathered from regional and national monitoring networks. The database is available for download from the World Data Centre for Precipitation Chemistry (http://wdcpc.org/)

  5. A global assessment of precipitation chemistry and deposition of sulfur, nitrogen, sea salt, base cations, organic acids, acidity and pH, and phosphorus

    NASA Astrophysics Data System (ADS)

    Vet, Robert; Artz, Richard S.; Carou, Silvina

    2014-08-01

    Investigating and assessing the chemical composition of precipitation and atmospheric deposition is essential to understanding how atmospheric pollutants contribute to contemporary environmental concerns including ecosystem acidification and eutrophication, loss of biodiversity, air pollution and global climate change. Evidence of the link between atmospheric deposition and these environmental issues is well established. The state of scientific understanding of this link is that present levels of atmospheric deposition of sulfur and nitrogen adversely affect terrestrial and aquatic ecosystems, putting forest sustainability and aquatic biodiversity at risk. Nitrogen and phosphorus loadings are linked to impacts on the diversity of terrestrial and aquatic vegetation through biological cycling, and atmospheric deposition plays a major role in the emission-transport-conversion-loss cycle of chemicals in the atmosphere as well as the formation of particulate matter and ozone in the troposphere. Evidence also shows that atmospheric constituents are changing the earth's climate through direct and indirect atmospheric processes. This Special Issue, comprising a single article titled "A global assessment of precipitation chemistry and deposition of sulfur, nitrogen, sea salt, base cations, organic acids, acidity and pH, and phosphorus", presents a recent comprehensive review of precipitation chemistry and atmospheric deposition at global and regional scales. The information in the Special Issue, including all supporting data sets and maps, is anticipated to be of great value not only to the atmospheric deposition community but also to other science communities including those that study ecosystem impacts, human health effects, nutrient processing, climate change, global and hemispheric modeling and biogeochemical cycling. Understanding and quantifying pollutant loss from the atmosphere is, and will remain, an important component of each of these scientific fields as they

  6. Insights from the metagenome of an acid salt lake: the role of biology in an extreme depositional environment.

    PubMed

    Johnson, Sarah Stewart; Chevrette, Marc Gerard; Ehlmann, Bethany L; Benison, Kathleen Counter

    2015-01-01

    The extremely acidic brine lakes of the Yilgarn Craton of Western Australia are home to some of the most biologically challenging waters on Earth. In this study, we employed metagenomic shotgun sequencing to generate a microbial profile of the depositional environment associated with the sulfur-rich sediments of one such lake. Of the 1.5 M high-quality reads generated, 0.25 M were mapped to protein features, which in turn provide new insights into the metabolic function of this community. In particular, 45 diverse genes associated with sulfur metabolism were identified, the majority of which were linked to either the conversion of sulfate to adenylylsulfate and the subsequent production of sulfide from sulfite or the oxidation of sulfide, elemental sulfur, and thiosulfate via the sulfur oxidation (Sox) system. This is the first metagenomic study of an acidic, hypersaline depositional environment, and we present evidence for a surprisingly high level of microbial diversity. Our findings also illuminate the possibility that we may be meaningfully underestimating the effects of biology on the chemistry of these sulfur-rich sediments, thereby influencing our understanding of past geobiological conditions that may have been present on Earth as well as early Mars. PMID:25923206

  7. Insights from the Metagenome of an Acid Salt Lake: The Role of Biology in an Extreme Depositional Environment

    PubMed Central

    Johnson, Sarah Stewart; Chevrette, Marc Gerard; Ehlmann, Bethany L.; Benison, Kathleen Counter

    2015-01-01

    The extremely acidic brine lakes of the Yilgarn Craton of Western Australia are home to some of the most biologically challenging waters on Earth. In this study, we employed metagenomic shotgun sequencing to generate a microbial profile of the depositional environment associated with the sulfur-rich sediments of one such lake. Of the 1.5 M high-quality reads generated, 0.25 M were mapped to protein features, which in turn provide new insights into the metabolic function of this community. In particular, 45 diverse genes associated with sulfur metabolism were identified, the majority of which were linked to either the conversion of sulfate to adenylylsulfate and the subsequent production of sulfide from sulfite or the oxidation of sulfide, elemental sulfur, and thiosulfate via the sulfur oxidation (Sox) system. This is the first metagenomic study of an acidic, hypersaline depositional environment, and we present evidence for a surprisingly high level of microbial diversity. Our findings also illuminate the possibility that we may be meaningfully underestimating the effects of biology on the chemistry of these sulfur-rich sediments, thereby influencing our understanding of past geobiological conditions that may have been present on Earth as well as early Mars. PMID:25923206

  8. Salt deposition at particle contact points

    NASA Astrophysics Data System (ADS)

    Nie, Xiaodong; Evitts, Richard W.; Besant, Robert W.; Kennell, Glyn F.

    2015-09-01

    Caking may occur when granular potash fertilizer with a moisture content greater than 0.25 % (w/w) undergoes drying. Since cake strength is proportional to the mass of crystal deposited per unit volume near contact points (and other factors) the modelling of mass deposition near contact points is important. The Young-Laplace equation for the air-salt-solution interface is used to determine the geometry of a 2-D planar saline film between two cubic potash particles. A 2-D theoretical model is developed and applied for ion diffusion and deposition near the contact point during drying. The numerical predictions of ion diffusion in an initially saturated salt illustrate the transient spatial distribution of new KCl deposits along the solid surfaces near the contact line. These results indicate the average salt deposition commences at the air-liquid-solid intersection, where the liquid film is thinnest, and moves toward the particle contact point with increasing area averaged KCl deposits, causing the formation of crystal deposits and bridges near contact points. It is concluded that the average salt deposit height increases inversely with distance from the contact point and decreases with initial contact angle of the contact region, but the deposition is nearly independent of the evaporation or drying rate near each contact region. Caking strength depends on, among other parameters, the amount of salt deposition near contact points.

  9. Stationary phase deposition based on onium salts

    DOEpatents

    Wheeler, David R.; Lewis, Patrick R.; Dirk, Shawn M.; Trudell, Daniel E.

    2008-01-01

    Onium salt chemistry can be used to deposit very uniform thickness stationary phases on the wall of a gas chromatography column. In particular, the stationary phase can be bonded to non-silicon based columns, especially microfabricated metal columns. Non-silicon microfabricated columns may be manufactured and processed at a fraction of the cost of silicon-based columns. In addition, the method can be used to phase-coat conventional capillary columns or silicon-based microfabricated columns.

  10. DRY DEPOSITION MODULE FOR REGIONAL ACID DEPOSITION

    EPA Science Inventory

    Methods to compute surface dry deposition velocities for sulfur dioxide, sulfate, ozone, NO plus NO2, and nitric acid vapor over much of the North American continent have been developed for use with atmospheric numerical models of long-range transport and deposition. The resultin...

  11. SOIL REACTION AND ACIDIC DEPOSITION

    EPA Science Inventory

    This chapter discusses the major chemical processes by which acidic deposition interacts with soils. he focus is on forest soils, as the effects of acidic deposition on soils used for production of food and fiber are generally small compared to effects of agricultural practices s...

  12. Mineralogical and geochemical characteristics of drinking water salt deposits

    NASA Astrophysics Data System (ADS)

    Soktoev, B. R.; Rikhvanov, L. P.; Matveenko, I. A.

    2015-11-01

    The article presents the research results on the features of element and mineral composition of salt deposits (limescale) formed in household conditions in heat exchanging equipment. The major part of limescale is represented by two species of calcium carbonate - calcite and aragonite. We have shown that high concentrations of chemical elements in the limescale promote the formation of their own mineral forms (sulphates, silicates, native forms) in salt deposits. Detecting such mineral formations suggests the salt deposits of drinking water to be a long-term storage media which can be used in the course of eco-geochemical and metallogenic studies.

  13. An innovative spraying setup to obtain uniform salt(s) mixture deposition to investigate hot corrosion

    NASA Astrophysics Data System (ADS)

    Mannava, Venkateswararao; Swaminathan, A. Vignesh; Kamaraj, M.; Kottada, Ravi Sankar

    2016-02-01

    A hot corrosion study via molten salt deposition and its interaction with creep/fatigue play a critical role in predicting the life of gas turbine engine components. To do systematic hot corrosion studies, deposition of molten salts on specimens should be uniform with good adherence. Thus, the present study describes an in-house developed spraying setup that produces uniform and reliable molten salt deposition in a repeatable fashion. The efficacy of the present method was illustrated by depositing 90 wt. % Na2SO4 + 5 wt. % NaCl + 5 wt. % NaV O3 salt mixture on hot corrosion coupons and on creep specimens, and also by comparing with other deposition methods.

  14. An innovative spraying setup to obtain uniform salt(s) mixture deposition to investigate hot corrosion.

    PubMed

    Mannava, Venkateswararao; Swaminathan, A Vignesh; Kamaraj, M; Kottada, Ravi Sankar

    2016-02-01

    A hot corrosion study via molten salt deposition and its interaction with creep/fatigue play a critical role in predicting the life of gas turbine engine components. To do systematic hot corrosion studies, deposition of molten salts on specimens should be uniform with good adherence. Thus, the present study describes an in-house developed spraying setup that produces uniform and reliable molten salt deposition in a repeatable fashion. The efficacy of the present method was illustrated by depositing 90 wt. % Na2SO4 + 5 wt. % NaCl + 5 wt. % NaVO3 salt mixture on hot corrosion coupons and on creep specimens, and also by comparing with other deposition methods. PMID:26931891

  15. 21 CFR 573.914 - Salts of volatile fatty acids.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Salts of volatile fatty acids. 573.914 Section 573... Food Additive Listing § 573.914 Salts of volatile fatty acids. (a) Identity. The food additive is a blend containing the ammonium or calcium salt of isobutyric acid and the ammonium or calcium salts of...

  16. 21 CFR 573.914 - Salts of volatile fatty acids.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Salts of volatile fatty acids. 573.914 Section 573... Food Additive Listing § 573.914 Salts of volatile fatty acids. (a) Identity. The food additive is a blend containing the ammonium or calcium salt of isobutyric acid and the ammonium or calcium salts of...

  17. Synthesis of acid addition salt of delta-aminolevulinic acid from 5-bromo levulinic acid esters

    DOEpatents

    Moens, Luc

    2003-06-24

    A process of preparing an acid addition salt of delta-aminolevulinc acid comprising: a) dissolving a lower alkyl 5-bromolevulinate and hexamethylenetetramine in a solvent selected from the group consisting of water, ethyl acetate, chloroform, acetone, ethanol, tetrahydrofuran and acetonitrile, to form a quaternary ammonium salt of the lower alkyl 5-bromolevulinate; and b) hydrolyzing the quaternary ammonium salt with an inorganic acid to form an acid addition salt of delta-aminolevulinic acid.

  18. ACID DEPOSITION AND FOREST DECLINE

    EPA Science Inventory

    The location, topography and other characteristics of the high-elevation forests of eastern North America cause them to be receptors of high levels of acid deposition and airborn trace metals. No other major forested areas in the U.S. are subjected to such intensely acid cloud mo...

  19. (Acidic deposition and the environment)

    SciTech Connect

    Garten, C.T.; Lindberg, S.E.; Van Miegroet, H.

    1990-10-24

    The travelers presented several papers at the Fourth International Conference on Acidic Deposition. These covered the following topics: atmospheric chemistry and deposition of airborne nitrogen compounds, soil solution chemistry in high-elevation spruce forests, and forest throughfall measurements for estimating total sulfur deposition to ecosystems. In addition, S. E. Lindberg was invited to organize and chair a conference session on Throughfall and Stemflow Experiments, and to present an invited lecture on Atmospheric Deposition and Canopy Interactions of Metals and Nitrogen in Forest Ecosystems: The Influence of Global Change'' at the 110th Anniversary Celebration of the Free University of Amsterdam.

  20. 78 FR 34338 - Citric Acid and Certain Citrate Salts From Canada: Preliminary Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-06-07

    ...: Antidumping Duty Orders, 74 FR 25703 (May 29, 2009) (Citric Acid Duty Orders). Methodology The Department has...: Assessment of Antidumping Duties, 68 FR 23954 (May 6, 2003). Cash Deposit Requirements The following deposit... International Trade Administration Citric Acid and Certain Citrate Salts From Canada: Preliminary Results...

  1. Boron deposition from fused salts. Final report

    SciTech Connect

    Smith, M.L.

    1980-08-01

    A partial evaluation of the feasibility of a process to electrodeposit pure coherent coatings of elemental boron from molten fluorides has been performed. The deposit produced was powdery and acicular, unless the fluoride melt was purified to have very low oxygen concentration. When the oxygen activity was reduced in the melt by addition of crystalline elemental boron, dense, amorphous boron deposit was produced. The boron deposits produced had cracks but were otherwise pure and dense and ranged up to 0.35 mm thick. Information derived during this project suggests that similar deposits might be obtained crack-free up to 1.00 mm thick by process modifications and improvements.

  2. 21 CFR 172.863 - Salts of fatty acids.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Salts of fatty acids. 172.863 Section 172.863 Food... Multipurpose Additives § 172.863 Salts of fatty acids. The food additive salts of fatty acids may be safely..., magnesium, potassium, and sodium salts of the fatty acids conforming with § 172.860 and/or oleic...

  3. 21 CFR 172.863 - Salts of fatty acids.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Salts of fatty acids. 172.863 Section 172.863 Food... Multipurpose Additives § 172.863 Salts of fatty acids. The food additive salts of fatty acids may be safely..., magnesium, potassium, and sodium salts of the fatty acids conforming with § 172.860 and/or oleic...

  4. 21 CFR 172.863 - Salts of fatty acids.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Salts of fatty acids. 172.863 Section 172.863 Food... Multipurpose Additives § 172.863 Salts of fatty acids. The food additive salts of fatty acids may be safely..., magnesium, potassium, and sodium salts of the fatty acids conforming with § 172.860 and/or oleic...

  5. Production of carboxylic acid and salt co-products

    DOEpatents

    Hanchar, Robert J.; Kleff, Susanne; Guettler, Michael V.

    2014-09-09

    This invention provide processes for producing carboxylic acid product, along with useful salts. The carboxylic acid product that is produced according to this invention is preferably a C.sub.2-C.sub.12 carboxylic acid. Among the salts produced in the process of the invention are ammonium salts.

  6. 40 CFR 721.1930 - Butanoic acid, antimony (3=) salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Butanoic acid, antimony (3=) salt. 721... Substances § 721.1930 Butanoic acid, antimony (3=) salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as butanoic acid, antimony (3=) salt (PMN...

  7. 40 CFR 721.1930 - Butanoic acid, antimony (3=) salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Butanoic acid, antimony (3=) salt. 721... Substances § 721.1930 Butanoic acid, antimony (3=) salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as butanoic acid, antimony (3=) salt (PMN...

  8. 40 CFR 721.1930 - Butanoic acid, antimony (3=) salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Butanoic acid, antimony (3=) salt. 721... Substances § 721.1930 Butanoic acid, antimony (3=) salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as butanoic acid, antimony (3=) salt (PMN...

  9. 40 CFR 721.1930 - Butanoic acid, antimony (3=) salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Butanoic acid, antimony (3=) salt. 721... Substances § 721.1930 Butanoic acid, antimony (3=) salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as butanoic acid, antimony (3=) salt (PMN...

  10. 40 CFR 721.1930 - Butanoic acid, antimony (3=) salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Butanoic acid, antimony (3=) salt. 721... Substances § 721.1930 Butanoic acid, antimony (3=) salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as butanoic acid, antimony (3=) salt (PMN...

  11. 40 CFR 721.9630 - Polyfluorosulfonic acid salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Polyfluorosulfonic acid salt. 721.9630... Substances § 721.9630 Polyfluorosulfonic acid salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as polyfluorosulfonic acid salt...

  12. 40 CFR 721.9630 - Polyfluorosulfonic acid salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Polyfluorosulfonic acid salt. 721.9630... Substances § 721.9630 Polyfluorosulfonic acid salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as polyfluorosulfonic acid salt...

  13. 40 CFR 721.9630 - Polyfluorosulfonic acid salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Polyfluorosulfonic acid salt. 721.9630... Substances § 721.9630 Polyfluorosulfonic acid salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as polyfluorosulfonic acid salt...

  14. 40 CFR 721.9630 - Polyfluorosulfonic acid salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Polyfluorosulfonic acid salt. 721.9630... Substances § 721.9630 Polyfluorosulfonic acid salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as polyfluorosulfonic acid salt...

  15. 40 CFR 721.9630 - Polyfluorosulfonic acid salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Polyfluorosulfonic acid salt. 721.9630... Substances § 721.9630 Polyfluorosulfonic acid salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as polyfluorosulfonic acid salt...

  16. (International conference on acidic deposition)

    SciTech Connect

    McLaughlin, S.B. Jr.

    1990-10-05

    The traveler took the opportunity to participate in a mini-sabbatical at the Institute of Terrestrial Ecology (ITE) in Edinburgh, Scotland, as a part of planned travel to Glasgow, Scotland, to attend the International Conference on Acidic Precipitation. The purpose of the sabbatical was to provide quality time for study and interchange of ideas with scientists at ITE working on physiological effects of acidic deposition and to allocate significant time for writing and synthesizing of results of physiological studies from the National Forest Response Program's Spruce/Fir Research Cooperative. The study focused on the very significant cytological and physiological effects of calcium deficiency in trees, a response that appears to be amplified in spruce by acidic deposition.

  17. Distribution of atmospheric marine salt depositions over Continental Western Europe.

    PubMed

    Delalieux, F; van Grieken, R; Potgieter, J H

    2006-06-01

    This contribution describes the distribution of marine salt aerosols in Belgium, France and Spain, as obtained from applying a kriging model to a set of data. The data was collected over a period of nine years and included wet as well as dry deposition results. It was found that the concentration of the salt particles decreased the fastest in Spain and the slowest in Belgium with increasing inland distance from the sea. These findings have implications for the degradation of monuments and historical buildings as a result of salt attack and ingress that often accompany degradation due to air pollution. PMID:16772114

  18. 21 CFR 172.863 - Salts of fatty acids.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Salts of fatty acids. 172.863 Section 172.863 Food... of fatty acids. The food additive salts of fatty acids may be safely used in food and in the... salts of the fatty acids conforming with § 172.860 and/or oleic acid derived from tall oil fatty...

  19. 40 CFR 721.2270 - Aliphatic dicarboxylic acid salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Aliphatic dicarboxylic acid salt. 721... Substances § 721.2270 Aliphatic dicarboxylic acid salt. (a) Chemical substance and significant new uses... salt (PMN P-92-1352) is subject to reporting under this section for the significant new uses...

  20. 40 CFR 721.7375 - Potassium salt of polyolefin acid.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Potassium salt of polyolefin acid. 721... Substances § 721.7375 Potassium salt of polyolefin acid. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a potassium salt of...

  1. 40 CFR 721.7375 - Potassium salt of polyolefin acid.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Potassium salt of polyolefin acid. 721... Substances § 721.7375 Potassium salt of polyolefin acid. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a potassium salt of...

  2. 40 CFR 721.7375 - Potassium salt of polyolefin acid.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Potassium salt of polyolefin acid. 721... Substances § 721.7375 Potassium salt of polyolefin acid. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a potassium salt of...

  3. 40 CFR 721.7375 - Potassium salt of polyolefin acid.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Potassium salt of polyolefin acid. 721... Substances § 721.7375 Potassium salt of polyolefin acid. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a potassium salt of...

  4. 40 CFR 721.7375 - Potassium salt of polyolefin acid.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Potassium salt of polyolefin acid. 721... Substances § 721.7375 Potassium salt of polyolefin acid. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a potassium salt of...

  5. 40 CFR 721.3629 - Triethanolamine salts of fatty acids.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Triethanolamine salts of fatty acids... Substances § 721.3629 Triethanolamine salts of fatty acids. (a) Chemical substances and significant new uses subject to reporting. (1) The chemical substances identified generically as triethanolamine salts of...

  6. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  7. 40 CFR 721.9650 - Tetramethylammonium salts of alkylbenzenesulfonic acid.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Tetramethylammonium salts of... Specific Chemical Substances § 721.9650 Tetramethylammonium salts of alkylbenzenesulfonic acid. (a... generically as tetramethylammonium salts of alkylbenzenesulfonic acid (PMN P-92-1364) is subject to...

  8. 40 CFR 721.3629 - Triethanolamine salts of fatty acids.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Triethanolamine salts of fatty acids... Substances § 721.3629 Triethanolamine salts of fatty acids. (a) Chemical substances and significant new uses subject to reporting. (1) The chemical substances identified generically as triethanolamine salts of...

  9. 40 CFR 721.9650 - Tetramethylammonium salts of alkylbenzenesulfonic acid.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Tetramethylammonium salts of... Specific Chemical Substances § 721.9650 Tetramethylammonium salts of alkylbenzenesulfonic acid. (a... generically as tetramethylammonium salts of alkylbenzenesulfonic acid (PMN P-92-1364) is subject to...

  10. 40 CFR 721.1650 - Alkylbenzenesulfonic acid and sodium salts.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... salts. 721.1650 Section 721.1650 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.1650 Alkylbenzenesulfonic acid and sodium salts. (a) Chemical substances... alkyl benzenesulfonic acid and sodium salts (PMNs P-88-1783, P-88-2231, P-88-2237, and P-88-2530)...

  11. 40 CFR 721.6140 - Dialkyldithiophosphoric acid, aliphatic amine salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ..., aliphatic amine salt. 721.6140 Section 721.6140 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.6140 Dialkyldithiophosphoric acid, aliphatic amine salt. (a) Chemical... as a dialkyldithiophosphoric acid, aliphatic amine salt (P-90-1839) is subject to reporting...

  12. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  13. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  14. 40 CFR 721.9650 - Tetramethylammonium salts of alkylbenzenesulfonic acid.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Tetramethylammonium salts of... Specific Chemical Substances § 721.9650 Tetramethylammonium salts of alkylbenzenesulfonic acid. (a... generically as tetramethylammonium salts of alkylbenzenesulfonic acid (PMN P-92-1364) is subject to...

  15. 40 CFR 721.9650 - Tetramethylammonium salts of alkylbenzenesulfonic acid.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Tetramethylammonium salts of... Specific Chemical Substances § 721.9650 Tetramethylammonium salts of alkylbenzenesulfonic acid. (a... generically as tetramethylammonium salts of alkylbenzenesulfonic acid (PMN P-92-1364) is subject to...

  16. 40 CFR 721.6140 - Dialkyldithiophosphoric acid, aliphatic amine salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ..., aliphatic amine salt. 721.6140 Section 721.6140 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.6140 Dialkyldithiophosphoric acid, aliphatic amine salt. (a) Chemical... as a dialkyldithiophosphoric acid, aliphatic amine salt (P-90-1839) is subject to reporting...

  17. 40 CFR 721.3629 - Triethanolamine salts of fatty acids.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Triethanolamine salts of fatty acids... Substances § 721.3629 Triethanolamine salts of fatty acids. (a) Chemical substances and significant new uses subject to reporting. (1) The chemical substances identified generically as triethanolamine salts of...

  18. 40 CFR 721.1650 - Alkylbenzenesulfonic acid and sodium salts.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... salts. 721.1650 Section 721.1650 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.1650 Alkylbenzenesulfonic acid and sodium salts. (a) Chemical substances... alkyl benzenesulfonic acid and sodium salts (PMNs P-88-1783, P-88-2231, P-88-2237, and P-88-2530)...

  19. 40 CFR 721.6140 - Dialkyldithiophosphoric acid, aliphatic amine salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ..., aliphatic amine salt. 721.6140 Section 721.6140 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.6140 Dialkyldithiophosphoric acid, aliphatic amine salt. (a) Chemical... as a dialkyldithiophosphoric acid, aliphatic amine salt (P-90-1839) is subject to reporting...

  20. 40 CFR 721.1650 - Alkylbenzenesulfonic acid and sodium salts.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... salts. 721.1650 Section 721.1650 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.1650 Alkylbenzenesulfonic acid and sodium salts. (a) Chemical substances... alkyl benzenesulfonic acid and sodium salts (PMNs P-88-1783, P-88-2231, P-88-2237, and P-88-2530)...

  1. 40 CFR 721.6140 - Dialkyldithiophosphoric acid, aliphatic amine salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ..., aliphatic amine salt. 721.6140 Section 721.6140 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.6140 Dialkyldithiophosphoric acid, aliphatic amine salt. (a) Chemical... as a dialkyldithiophosphoric acid, aliphatic amine salt (P-90-1839) is subject to reporting...

  2. 40 CFR 721.1650 - Alkylbenzenesulfonic acid and sodium salts.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... salts. 721.1650 Section 721.1650 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.1650 Alkylbenzenesulfonic acid and sodium salts. (a) Chemical substances... alkyl benzenesulfonic acid and sodium salts (PMNs P-88-1783, P-88-2231, P-88-2237, and P-88-2530)...

  3. 40 CFR 721.3629 - Triethanolamine salts of fatty acids.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Triethanolamine salts of fatty acids... Substances § 721.3629 Triethanolamine salts of fatty acids. (a) Chemical substances and significant new uses subject to reporting. (1) The chemical substances identified generically as triethanolamine salts of...

  4. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  5. 40 CFR 721.9650 - Tetramethylammonium salts of alkylbenzenesulfonic acid.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Tetramethylammonium salts of... Specific Chemical Substances § 721.9650 Tetramethylammonium salts of alkylbenzenesulfonic acid. (a... generically as tetramethylammonium salts of alkylbenzenesulfonic acid (PMN P-92-1364) is subject to...

  6. 40 CFR 721.6140 - Dialkyldithiophosphoric acid, aliphatic amine salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ..., aliphatic amine salt. 721.6140 Section 721.6140 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.6140 Dialkyldithiophosphoric acid, aliphatic amine salt. (a) Chemical... as a dialkyldithiophosphoric acid, aliphatic amine salt (P-90-1839) is subject to reporting...

  7. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  8. 40 CFR 721.1650 - Alkylbenzenesulfonic acid and sodium salts.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... salts. 721.1650 Section 721.1650 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.1650 Alkylbenzenesulfonic acid and sodium salts. (a) Chemical substances... alkyl benzenesulfonic acid and sodium salts (PMNs P-88-1783, P-88-2231, P-88-2237, and P-88-2530)...

  9. 40 CFR 721.3629 - Triethanolamine salts of fatty acids.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Triethanolamine salts of fatty acids... Substances § 721.3629 Triethanolamine salts of fatty acids. (a) Chemical substances and significant new uses subject to reporting. (1) The chemical substances identified generically as triethanolamine salts of...

  10. Acid deposition in east Asia

    SciTech Connect

    Phadnis, M.J.; Carmichael, G.R.; Ichikawa, Y.

    1996-12-31

    A comparison between transport models was done to study the acid deposition in east Asia. The two models in question were different in the way the treated the pollutant species and the way simulation was carried out. A single-layer, trajectory model with simple (developed by the Central Research Institute of Electric Power Industry (CRIEPI), Japan) was compared with a multi-layered, eulerian type model (Sulfur Transport Eulerian Model - II [STEM-II]) treating the chemical processes in detail. The acidic species used in the simulation were sulfur dioxide and sulfate. The comparison was done for two episodes: each a month long in winter (February) and summer (August) of 1989. The predicted results from STEM-II were compared with the predicted results from the CRIEPI model as well as the observed data at twenty-one stations in Japan. The predicted values from STEM-II were similar to the ones from the CRIEPI results and the observed values in regards to the transport features. The average monthly values of SO{sub 2} in air, sulfate in air and sulfate in precipitation were in good agreement. Sensitivity studies were carried out under different scenarios of emissions, dry depositions velocities and mixing heights. The predicted values in these sensitivity studies showed a strong dependence on the mixing heights. The predicted wet deposition of sulfur for the two months is 0.7 gS/m2.mon, while the observed deposition is around 1.1 gS/m2.mon. It was also observed that the wet deposition on the Japan sea side of the islands is more than those on the Pacific side and the Okhotsk sea, mainly because of the continental outflow of pollutant air masses from mainland China and Korea. The effects of emissions from Russia and volcanoes were also evaluated.

  11. 21 CFR 172.350 - Fumaric acid and salts of fumaric acid.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Fumaric acid and salts of fumaric acid. 172.350... HUMAN CONSUMPTION Special Dietary and Nutritional Additives § 172.350 Fumaric acid and salts of fumaric acid. Fumaric acid and its calcium, ferrous, magnesium, potassium, and sodium salts may be safely...

  12. 21 CFR 172.350 - Fumaric acid and salts of fumaric acid.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Fumaric acid and salts of fumaric acid. 172.350... HUMAN CONSUMPTION Special Dietary and Nutritional Additives § 172.350 Fumaric acid and salts of fumaric acid. Fumaric acid and its calcium, ferrous, magnesium, potassium, and sodium salts may be safely...

  13. 21 CFR 172.350 - Fumaric acid and salts of fumaric acid.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Fumaric acid and salts of fumaric acid. 172.350... HUMAN CONSUMPTION Special Dietary and Nutritional Additives § 172.350 Fumaric acid and salts of fumaric acid. Fumaric acid and its calcium, ferrous, magnesium, potassium, and sodium salts may be safely...

  14. Geologic appraisal of Paradox basin salt deposits for water emplacement

    USGS Publications Warehouse

    Hite, R.J.; Lohman, Stanley William

    1973-01-01

    Thick salt deposits of Middle Pennsylvanian age are present in an area of 12,000 square miles in the Paradox basin of southeast Utah and southwest Colorado. The deposits are in the Paradox Member of the Hermosa Formation. The greatest thickness of this evaporite sequence is in a troughlike depression adjacent to the Uncompahgre uplift on the northeast side of the basin. The salt deposits consist of a cyclical sequence of thick halite units separated by thin units of black shale, dolomite, and anhydrite. Many halite units are several hundred feet thick and locally contain economically valuable potash deposits. Over much of the Paradox basin the salt deposits occur at depths of more than 5,000 feet. Only in a series of salt anticlines located along the northeastern side of the basin do the salt deposits rise to relatively shallow depths. The salt anticlines can be divided geographically and structurally into five major systems. Each system consists of a long undulating welt of thickened salt over which younger rocks are arched in anticlinal form. Locally there are areas along the axes of the anticlines where the Paradox Member was never covered by younger sediments. This allowed large-scale migration of Paradox strata toward and up through these holes in the sediment cover forming diapiric anticlines. The central or salt-bearing cores of tthe anticlines range in thickness from about 2,500 to 14,000 feet. Structure in the central core of the salt anticlines is the result of both regional-compression and flowage of the Paradox Member into the anticlines from adjacent synclines. Structure in the central cores of the salt anticlines ranges from relatively undeformed beds to complexly folded and faulted masses, in which stratigraphic continuity is undemonstrable. The presence of thick cap rock .over many of the salt anticlines is evidence of removal of large volumes of halite by groundwater. Available geologic and hydrologic information suggests that this is a relatively

  15. Phyllosilicate and Salt Layering in Intraplaya Deposits, Analogs for Martian Layered Deposits

    NASA Astrophysics Data System (ADS)

    Baldridge, A. M.; Thomson, B. J.

    2013-12-01

    The evolution of the martian climate is recorded in its sedimentological and stratigraphic record. Thick sequences of layered, martian sedimentary materials commonly contain phyllosilicates overlain by sulfate- and other salt-bearing units and are thought to record the transition between neutral pH aqueous alteration in the Noachian to an acidic evaporitic system in the late Noachian to the Hesperian. In some locations on Mars, however, phyllosilicates and sulfates are interbedded, occur in close proximity as in Gale Crater, allowing the examination of their temporal and geochemical relationship. Although the model of linear evolution is consistent with the 'drying out' of Mars over time and thus provides an important framework, it is possible and indeed perhaps likely that regional differences in aqueous geochemistry were prevalent and are preserved in the martian rock record. Playa basins in WA provide an opportunity to study compositional variability and formation processes and correlate remote sensing with in situ observations. The objectives of this study are designed to integrate Mars analog surface and subsurface sampling with results from remote sensing data to better understand the formation, evolution and preservation of the sequences of layered sulfate and phyllosilicate deposits on Mars and the interpretations that can be made from remote sensing. To this end, we have obtained and processed hyperspectral remotely sensed VIS/NIR data for 3 dry lakes in Western Australia: Lake Gilmore, Lake Brown and Lake Chandler. Additionally, 7 shallow cores were collected from representative deposits in each of these basins. Each of these sedimentary basins exhibits surface compositional variability in sulfate, chloride and phyllosilicate deposits. The core samples have been spectrally cataloged and show similar variability and mixing. Together with the spectral variability seen form remote sensing at the surface, these results record the sedimentary history of the

  16. Comparison of Membrane ATPases from Extreme Halophiles Isolated from Ancient Salt Deposits

    NASA Technical Reports Server (NTRS)

    Stan-Lotter, Helga; Sulzner, Michael; Egelseer, Eva; Norton, Cynthia F.; Hochstein, Lawrence I.

    1993-01-01

    Halophilic microorganisms were isolated from Triassic and Permian salt deposits. Two were rods and grew as red colonies; another was a coccus and produced pink colonies. The rods lysed in solutions that lacked added sodium chloride. Growth of all isolates was inhibited by aphidicolin and their bulk proteins were acidic as judged from isoelectric focusing. Therefore, these organisms were tentatively identified as extreme halophiles. Whole cell proteins patterns of the isolates following gel electrophoresis were distinct and differed from those of representative type strains of halophilic bacteria. The membrane ATPases from the rods were similar to the enzyme from Halobacterium saccharovorum with respect to sub unit composition. enzymatic properties and immunological cross-reaction, but differed slightly in amino acid composition. If the age of the microbial isolated is similar to that of the salt deposits, they can be considered repositories of molecular information of great evolutionary interest.

  17. Comparison of membrane ATPases from extreme halophiles isolated from ancient salt deposits

    NASA Astrophysics Data System (ADS)

    Stan-Lotter, Helga; Sulzner, Michael; Egelseer, Eva; Norton, Cynthia F.; Hochstein, Lawrence I.

    1993-02-01

    Halophilic microorganisms were isolated from Triassic and Permian salt deposits. Two were rods and grew as red colonies; another was a coccus and produced pink colonies. The rods lysed in solutions that lacked added sodium chloride. Growth of all isolates was inhibited by aphidicolin and their bulk proteins were acidic as judged from isoelectric focusing. Therefore, these organisms were tentatively identified as extreme halophiles. Whole cell proteins patterns of the isolates following gel electrophoresis were distinct and differed from those of representative type strains of halophilic bacteria. The membrane ATPases from the rods were similar to the enzyme fromHalobacterium saccharovorum with respect to subunit composition, enzymatic properties and immunological cross-reaction, but differed slightly in amino acid composition. If the age of the microbial isolated is similar to that of the salt deposits, they can be considered repositories of molecular information of great evolutionary interest.

  18. Comparison of membrane ATPases from extreme halophiles isolated from ancient salt deposits

    NASA Technical Reports Server (NTRS)

    Stan-Lotter, Helga; Sulzner, Michael; Egelseer, Eva; Norton, Cynthia F.; Hochstein, Lawrence I.

    1993-01-01

    Halophilic microorganisms were isolated from Triassic and Permian salt deposits. Two were rods and grew as red colonies; another was a coccus and produced pink colonies. The rods lysed in solutions that lacked added sodium chloride. Growth of all isolates was inhibited by aphidicolin and their bulk-proteins were acidic as judged from isoelectric focusing. Therefore, these organisms were tentatively identified as extreme halophiles. Whole cell proteins patterns of the isolates following gel electrophoresis were distinct and differed from those of representative type strains of halophilic bacteria. The membrane ATPases from the rods were similar to the enzyme from Halobacterium saccharovorum with respect to subunit composition, enzymatic properties and immunological cross-reaction, but differed slightly in amino acid composition. If the age of the microbial isolated is similar to that of the salt deposits, they can be considered repositories of molecular information of great evolutionary interest.

  19. 21 CFR 172.863 - Salts of fatty acids.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... Multipurpose Additives § 172.863 Salts of fatty acids. The food additive salts of fatty acids may be safely... conditions: (a) The additive consists of one or any mixture of two or more of the aluminum, calcium... derived from tall oil fatty acids conforming with § 172.862. (b) The food additive is used or intended...

  20. 21 CFR 172.350 - Fumaric acid and salts of fumaric acid.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... acid. Fumaric acid and its calcium, ferrous, magnesium, potassium, and sodium salts may be safely used... anhydrous basis. (2) The calcium, magnesium, potassium, and sodium salts contain a minimum of 99 percent...

  1. Transpiring wall supercritical water oxidation reactor salt deposition studies

    SciTech Connect

    Haroldsen, B.L.; Mills, B.E.; Ariizumi, D.Y.; Brown, B.G.

    1996-09-01

    Sandia National Laboratories has teamed with Foster Wheeler Development Corp. and GenCorp, Aerojet to develop and evaluate a new supercritical water oxidation reactor design using a transpiring wall liner. In the design, pure water is injected through small pores in the liner wall to form a protective boundary layer that inhibits salt deposition and corrosion, effects that interfere with system performance. The concept was tested at Sandia on a laboratory-scale transpiring wall reactor that is a 1/4 scale model of a prototype plant being designed for the Army to destroy colored smoke and dye at Pine Bluff Arsenal in Arkansas. During the tests, a single-phase pressurized solution of sodium sulfate (Na{sub 2}SO{sub 4}) was heated to supercritical conditions, causing the salt to precipitate out as a fine solid. On-line diagnostics and post-test observation allowed us to characterize reactor performance at different flow and temperature conditions. Tests with and without the protective boundary layer demonstrated that wall transpiration provides significant protection against salt deposition. Confirmation tests were run with one of the dyes that will be processed in the Pine Bluff facility. The experimental techniques, results, and conclusions are discussed.

  2. 21 CFR 573.914 - Salts of volatile fatty acids.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food Additive Listing § 573.914 Salts of volatile fatty acids. (a) Identity. The food additive is a... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Salts of volatile fatty acids. 573.914 Section...

  3. 21 CFR 573.914 - Salts of volatile fatty acids.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food Additive Listing § 573.914 Salts of volatile fatty acids. (a) Identity. The food additive is a... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Salts of volatile fatty acids. 573.914 Section...

  4. 40 CFR 721.2270 - Aliphatic dicarboxylic acid salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Aliphatic dicarboxylic acid salt. 721... Substances § 721.2270 Aliphatic dicarboxylic acid salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as aliphatic dicarboxylic...

  5. 40 CFR 721.2270 - Aliphatic dicarboxylic acid salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Aliphatic dicarboxylic acid salt. 721... Substances § 721.2270 Aliphatic dicarboxylic acid salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as aliphatic dicarboxylic...

  6. 40 CFR 721.2270 - Aliphatic dicarboxylic acid salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Aliphatic dicarboxylic acid salt. 721... Substances § 721.2270 Aliphatic dicarboxylic acid salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as aliphatic dicarboxylic...

  7. 40 CFR 721.2270 - Aliphatic dicarboxylic acid salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Aliphatic dicarboxylic acid salt. 721... Substances § 721.2270 Aliphatic dicarboxylic acid salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as aliphatic dicarboxylic...

  8. 40 CFR 721.1648 - Substituted benzenesulfonic acid salt (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Substituted benzenesulfonic acid salt (generic). 721.1648 Section 721.1648 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.1648 Substituted benzenesulfonic acid salt (generic). (a)...

  9. 40 CFR 721.1648 - Substituted benzenesulfonic acid salt (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Substituted benzenesulfonic acid salt (generic). 721.1648 Section 721.1648 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.1648 Substituted benzenesulfonic acid salt (generic). (a)...

  10. 40 CFR 721.1648 - Substituted benzenesulfonic acid salt (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Substituted benzenesulfonic acid salt (generic). 721.1648 Section 721.1648 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.1648 Substituted benzenesulfonic acid salt (generic). (a)...

  11. 40 CFR 721.1648 - Substituted benzenesulfonic acid salt (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Substituted benzenesulfonic acid salt (generic). 721.1648 Section 721.1648 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.1648 Substituted benzenesulfonic acid salt (generic). (a)...

  12. 40 CFR 721.1648 - Substituted benzenesulfonic acid salt (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Substituted benzenesulfonic acid salt (generic). 721.1648 Section 721.1648 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.1648 Substituted benzenesulfonic acid salt (generic). (a)...

  13. 40 CFR 721.2086 - Coco acid triamine condensate, polycarboxylic acid salts.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Coco acid triamine condensate... Specific Chemical Substances § 721.2086 Coco acid triamine condensate, polycarboxylic acid salts. (a... coco acid triamine condensate, poly-car-box-ylic acid salts. (PMN P-92-446) is subject to...

  14. 40 CFR 721.2086 - Coco acid triamine condensate, polycarboxylic acid salts.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Coco acid triamine condensate... Specific Chemical Substances § 721.2086 Coco acid triamine condensate, polycarboxylic acid salts. (a... coco acid triamine condensate, poly-car-box-ylic acid salts. (PMN P-92-446) is subject to...

  15. The dry deposition of mercury into the Great Salt Lake

    NASA Astrophysics Data System (ADS)

    Lisonbee, Joel R.

    The Great Salt Lake (GSL) in the western United States has been identified as the most mercury laden body of water in the United States with a median water mercury concentration of 42 nanograms per liter. When Hg enters an aquatic ecosystem, it can be converted to the toxic organic mercury compound, methylmercury. Methylmercury bioaccumulates up the food chain and has been the cause of consumption advisories for game fish in many lakes and rivers in the historically pristine Intermountain West. In 2005, the Utah Department of Health and the Fish and Wildlife Service placed a similar consumption advisory on waterfowl on the GSL. The primary goal of this study is to identify the pathway of greatest influx of Hg pollution to the GSL to give insight toward the source and an eventual solution to the Hg pollution problem. Speciated atmospheric mercury measurements were collected at a field site on the eastern shore of the GSL for a 1-year period beginning on July 1, 2009. These atmospheric mercury concentrations, along with turbulence measurements, were used as input to a resistance-in-series dry deposition model (based on Wesley and Hicks 1977). The dry deposition flux of mercury was determined from the modeled dry deposition velocity and the measured concentrations. This dry deposition flux was compared to the wet deposition flux measured by the National Deposition Network and the riverine influx measured by the USGS. It was found that in the 1 year from July 1, 2009 through June 30, 2010, 10.7 nanograms per square meter of Hg was deposited into the GSL by dry deposition from the atmosphere. Dry deposition makes up 60% of the total Hg influx from all measured pathways. The flux from the dry deposition of the global background pool of Hg (1.5 +/- 0.2 nanograms per square meter) dominated the dry deposition flux, making up 82.5+/-8.5% of the dry deposition flux and 50% of the total Hg influx to the GSL. Lake sediment cores from the GSL suggest a much larger annual flux

  16. ADVANCES IN CONTROL TECHNOLOGY FOR ACID DEPOSITION

    EPA Science Inventory

    Causes and effects of acid deposition are the subject of widespread discussion both in the U.S. and Europe. Two major concerns are the acidification of lakes and streams, and forest damage. The proposed mechanism for acidification of lakes and streams is the deposition of acidic ...

  17. ACIDIC DEPOSITION AND CISTERN DRINKING WATER SUPPLIES

    EPA Science Inventory

    The Water quality charecteristics, including the trace element Cd, cu, Pb, and Zn, in rainwater cistern supplies representing an area receiving acidic deposition were compared to cistern water chemistry in a control area that does not receive a significant input of acidic deposit...

  18. Mesoscale acid deposition modeling studies

    NASA Technical Reports Server (NTRS)

    Kaplan, Michael L.; Proctor, F. H.; Zack, John W.; Karyampudi, V. Mohan; Price, P. E.; Bousquet, M. D.; Coats, G. D.

    1989-01-01

    The work performed in support of the EPA/DOE MADS (Mesoscale Acid Deposition) Project included the development of meteorological data bases for the initialization of chemistry models, the testing and implementation of new planetary boundary layer parameterization schemes in the MASS model, the simulation of transport and precipitation for MADS case studies employing the MASS model, and the use of the TASS model in the simulation of cloud statistics and the complex transport of conservative tracers within simulated cumuloform clouds. The work performed in support of the NASA/FAA Wind Shear Program included the use of the TASS model in the simulation of the dynamical processes within convective cloud systems, the analyses of the sensitivity of microburst intensity and general characteristics as a function of the atmospheric environment within which they are formed, comparisons of TASS model microburst simulation results to observed data sets, and the generation of simulated wind shear data bases for use by the aviation meteorological community in the evaluation of flight hazards caused by microbursts.

  19. Structural evolution of Alpine salt deposits, Austria and Bavaria

    NASA Astrophysics Data System (ADS)

    Leitner, Ch.; Neubauer, F.; Genser, H.; Borojevic Sostaric, S.

    2009-04-01

    Structural evolution of Alpine salt deposits, Austria and Bavaria Alpine salt deposits consist of a tectonic melange of rocksalt and shale called haselgebirge representing the Haselgebirge Formation of Permian to Early Triassic age and mainly exposed within the central and eastern Northern Calcareous Alps. The initial evaporitic sediments were transformed into a breccia (protocataclasite, mylonite) during Alpine orogeny. Residual rocks of shale, anhydrite, polyhalite, sandstone and limestone float as isolated bodies in the haselgebirge matrix. Field investigations of foliation, halite mineral lineation, fold axis, veins and the overall present slickensides in shale revealed an individual history for all investigated mines (Dürrnberg, Berchtesgaden, Altaussee, in part Hallstatt). Ar-Ar dating of various micostructural types of polyhalite yield several preliminary age groups: 235 Ma, 180 Ma, and 110 Ma. Fluid inclusion measurements on anhydrite together with vitrinite reflectance data showed that temperatures of 140-180 °C were reached in Berchtesgaden and around 250° C in Altaussee. Microstructural analysis of anhydrite reveals strong stretching structures with lobate grain boundaries and the fomation of large anhydrite crystals in polyhalite (locally called muriazite). Rock salt and Haselgebirge samples were gamma-irradiated to intensify contrasts in thin section analysis. No primary structures like fluid inclusion bands or chevrons were found. The oldest visible parts are innner cores of large residual grains. All other types of grains suffered grain size reduction during the subsequent deformation. Using subgrain piezometry, high differential stresses of around 5 MPa formed the present microstructure. The Alpine rock salt deposits suffered a complex deformation history. A first peak was the formation of polyhalite veins, 235 Ma ago. The overburden was around 800 m (Rantitsch & Russegger, 2005) and first differentiation of the sea floor occurred (Mandl, 1984

  20. 40 CFR 721.2086 - Coco acid triamine condensate, polycarboxylic acid salts.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Coco acid triamine condensate, polycarboxylic acid salts. 721.2086 Section 721.2086 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.2086 Coco acid triamine condensate, polycarboxylic acid salts....

  1. 40 CFR 721.3620 - Fatty acid amine condensate, polycarboxylic acid salts.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Fatty acid amine condensate, polycarboxylic acid salts. 721.3620 Section 721.3620 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3620 Fatty acid amine condensate, polycarboxylic acid salts....

  2. 40 CFR 721.3620 - Fatty acid amine condensate, polycarboxylic acid salts.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Fatty acid amine condensate, polycarboxylic acid salts. 721.3620 Section 721.3620 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3620 Fatty acid amine condensate, polycarboxylic acid salts....

  3. 40 CFR 721.3620 - Fatty acid amine condensate, polycarboxylic acid salts.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Fatty acid amine condensate, polycarboxylic acid salts. 721.3620 Section 721.3620 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3620 Fatty acid amine condensate, polycarboxylic acid salts....

  4. 40 CFR 721.3620 - Fatty acid amine condensate, polycarboxylic acid salts.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Fatty acid amine condensate, polycarboxylic acid salts. 721.3620 Section 721.3620 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3620 Fatty acid amine condensate, polycarboxylic acid salts....

  5. 40 CFR 721.2086 - Coco acid triamine condensate, polycarboxylic acid salts.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Coco acid triamine condensate, polycarboxylic acid salts. 721.2086 Section 721.2086 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.2086 Coco acid triamine condensate, polycarboxylic acid salts....

  6. 40 CFR 721.2086 - Coco acid triamine condensate, polycarboxylic acid salts.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Coco acid triamine condensate, polycarboxylic acid salts. 721.2086 Section 721.2086 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.2086 Coco acid triamine condensate, polycarboxylic acid salts....

  7. 40 CFR 721.3620 - Fatty acid amine condensate, polycarboxylic acid salts.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Fatty acid amine condensate, polycarboxylic acid salts. 721.3620 Section 721.3620 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3620 Fatty acid amine condensate, polycarboxylic acid salts....

  8. On the Existence of Hydrogen Salts of Monoprotic Acids

    ERIC Educational Resources Information Center

    Stojanovska, Marina I.; Petrusevski, Vladimir M.; Soptrajanov, Bojan T.

    2012-01-01

    The notion that acid salts exist only for diprotic and polyprotic acids is found in many high school and university textbooks, although the "only" condition is not always stated explicitly. A fairly simple experiment shows that there is a pronounced exothermic effect when pure acetic acid is added to potassium acetate. Experiments with similar…

  9. Direct esterification of ammonium salts of carboxylic acids

    DOEpatents

    Halpern, Yuval

    2003-06-24

    A non-catalytic process for producing esters, the process comprising reacting an ammonium salt of a carboxylic acid with an alcohol and removing ammonia from the reaction mixture. Selectivities for the desired ester product can exceed 95 percent.

  10. Effects of acid deposition on agricultural production

    SciTech Connect

    Moskowitz, P.D.; Medeiros, W.H.; Oden, N.L.; Thode, H.C. Jr.; Coveney, E.A.; Jacobson, J.S.; Rosenthal, R.E.; Evans, L.S.; Lewin, K.F.; Allen, F.L.

    1985-09-01

    A preliminary assessment, both qualitative and quantitative, was carried out on the effects of acid deposition on agriculture. An inventory was made of US crops exposed to different acid deposition levels in 1982. Most crops (valued at more than $50 billion) were exposed to annual average acid deposition levels greater than pH 4.6, but crops worth more than $220 billion were exposed to even lower pH levels. Published results of experiments on crop response to acid deposition have not identified any single crop as being consistently sensitive, and suggest that present levels of acidic precipitation in the US are not significantly affecting growth and yield of crops. Because relatively few experiments appropriate to a quantitative acid deposition assessment have been conducted, the quantitative section is necessarily based on a restricted data set. Corn, potatoes, and soybeans have been studied in experimental environments which simulate agronomic conditions and which have adequate statistical power for yield estimates; only some varieties of soybeans have demonstrated statistically significant sensitivity to acid deposition.

  11. ACIDIC DEPOSITION PHENOMENON AND ITS EFFECTS: CRITICAL ASSESSMENT DOCUMENT

    EPA Science Inventory

    The Acidic Deposition Phenomenon and Its Effects: Critical Assessment Document (CAD) is a summary, integration, and interpretation of the current scientific understanding of acidic deposition. It is firmly based upon The Acidic Deposition Phenomenon and Its Effects: Critical Asse...

  12. ATMOSPHERIC ACID DEPOSITION DAMAGE TO PAINTS

    EPA Science Inventory

    Available data from laboratory and field studies of damage to paints by erosion have been analyzed to develop an atmospheric acid deposition damage function for exterior house paints containing calcium carbonate or silicate extenders. Regression analysis coefficients associated w...

  13. Cotton fabrics with UV blocking properties through metal salts deposition

    NASA Astrophysics Data System (ADS)

    Emam, Hossam E.; Bechtold, Thomas

    2015-12-01

    Exposure to sunlight is important for human health as this increases the resistance to diverse pathogens, but the higher doses cause skin problems and diseases. Hence, wearing of sunlight protective fabrics displays a good solution for people working in open atmosphere. The current study offered quite simple and technically feasible ways to prepare good UV protection fabrics based on cotton. Metal salts including Zn, Cu and Ti were immobilized into cotton and oxidized cotton fabrics by using pad-dry-cure technique. Metal contents on fabrics were determined by AAS; the highest metal content was recorded for Cu-fabric and it was 360.6 mmol/kg after treatment of oxidized cotton with 0.5 M of copper nitrate. Ti contents on fabrics were ranged between 168.0 and 200.8 mmol/kg and it showed the lowest release as only 38.1-46.4% leached out fabrics after five laundry washings. Metal containing deposits were specified by scanning electron microscopy and energy dispersive X-ray spectroscopy. UV-transmission radiation over treated fabrics was measured and ultraviolet protection factor (UPF) was calculated. UPF was enhanced after treatment with Cu and Ti salts to be 11.6 and 14, respectively. After five washings, the amount of metal (Cu or Ti) retained indicates acceptable laundering durability.

  14. Florida acid deposition study - an overview

    SciTech Connect

    Henderson, C.D.; Hendrickson, E.R.

    1983-01-01

    Comprehensive literature searches were performed in the areas of source attribution and long-range transport and ecological and material effects. The literature searches were designed to determine the impacts of acid deposition that are specific to Florida. In January 1982 the results of Phase I programs were issued. These reports were: (1) Monitoring Program Phase I Summary Report; (2) Source Attribution Phase I Summary Report; and (3) A Literature Review of the Ecological and Materials Effects of Acid Deposition.

  15. Acidic deposition and soil processes

    SciTech Connect

    Newton, R.M.; April, R.H.

    1985-08-01

    The results of the Integrated Lake-Watershed Acidification Study (ILWAS) show that the sensitivity of a watershed to surface water acidification is determined by the flow paths of water through the terrestrial system. If the water infiltrates through the soils into the groundwater system, acid neutralization occurs through weathering reactions involving minerals in the soils and till. Runoff and shallow interflow result in acid surface waters. Flow paths are determined in the ILWAS watersheds by the thickness of the glacial till. Complete neutralization can occur even in areas underlain by sensitive bedrock if the flow path through the mineral horizons is long enough. This appears to hold even in areas outside of the Adirondacks. 11 references, 5 figures.

  16. Aptian depositional patterns influenced by salt tectonics, central east Texas basin

    SciTech Connect

    Lomando, A.J.; Birdsall, T.P.

    1989-03-01

    Salt tectonics, which lead both directly and indirectly to the formation of paleobathymetric highs, peripheral sinks and persistent structural highs, strongly influenced carbonate and siliciclastic depositional patterns of the Aptian Rodessa Formation. This study has focused on northern Anderson County, located in the axial portion of what was the broad, shallow East Texas basin shelf during deposition of the Rodessa. Five Louann (Bathonian-Callovian) Salt diapirs were active and had significant impact on Aptian depositional patterns.

  17. [Prokaryotic microbial diversity of the ancient salt deposits in the Kunming Salt Mine, P.R. China].

    PubMed

    Xiao, Wei; Peng, Qian; Liu, Hong-wei; Wen, Meng-liang; Cui, Xiao-long; Yang, Ya-ling; Duan, Dong-cheng; Chen, Wei; Deng, Lan; Li, Qin-yuan; Chen, Yi-guang; Wang, Zhi-gang; Ren, Zhen; Liu, Ji-hui

    2007-04-01

    The prokaryotic microbial diversity of the ancient salt deposits in the Kunming Salt Mine, PR China was investigated using PCR-DGGE and rRNA approaches. Total community DNA was extracted and purified by a direct method, which yielded amplified DNA of high molecular weight for samples. A variable region of 16S rRNA gene was then amplified by PCR with bacterial and archaeal primers and analyzed by denaturing gradient gel electrophoresis (DGGE). Twenty-seven major bands were detected in the bacterial DGGE profile of the sample, but only one band of pure culture strains of bacteria isolated from the Kunming Salt Mine matched with one band of sample. No band of pure culture strains of archaea isolated from the Kunming Salt Mine matched with 18 major bands of sample. The results indicated that most of microbes in this environment are likely uncultivable. Clones on the plate were not the predominant species in the community. Two 16S rRNA gene clone libraries (bacteria and archaea) were also constructed, and 36 and 20 clones were selected for amplified ribosomal DNA restriction analysis (ARDRA). ARDRA with enzymes Afa I, Hha I, Hae III revealed 10 bacterial operational taxonomic units (OTUs), with three most abundant OTUs accounting for 38.9%, 25.0%, 16.7% of all the bacterial 16S rDNA clones, respectively. The remaining 7 OTUs presented at low levels, were represented by a single clone. Eight archaeal OTUs were obtained but no predominant OTUs. Some clones were sequenced and each sequence was compared with all nucleotide sequences in GenBank database. Examination of 16S rDNA clones showed that the ancient salt deposits in the Kunming Salt Mine contained a phylogenetically diverse population of organisms from the Bacteria domain with members of three major lineages represented: alpha-proteobacteria, gamma-Proteobacteria and Actinobacteria, especially Pseudomonas. Surprisingly, we recovered a variety of sequence closely related to Actinobacteria which was not found in other

  18. Origin of fluid inclusion water in bedded salt deposits, Palo Duro Basin, Texas

    SciTech Connect

    Knauth, L.P.; Beeunas, M.A.

    1985-07-01

    Salt horizons in the Palo Duro Basin being considered for repository sites contain fluid inclusions which may represent connate water retained in the salt from the time of original salt deposition and/or external waters which have somehow penetrated the salt. The exact origin of this water is important to the question of whether or not internal portions of the salt deposit have been, and are likely to be, isolated from the hydrosphere for long periods of time. The /sup 18/O//sup 16/O and D/H ratios measured for water extracted from solid salt samples show the inclusions to be dissimilar in isotopic composition to meteoric waters and to formation waters above and below the salt. The fluid inclusions cannot be purely external waters which have migrated into the salt. The isotope data are readily explained in terms of mixed meteoric-marine connate evaporite waters which date back to the time of deposition and early diagenesis of the salt (>250 million years). Any later penetration of the salt by meteoric waters has been insufficient to flush out the connate brines.

  19. Constraints on the composition and particle size of chloride salt-bearing deposits on Mars

    NASA Astrophysics Data System (ADS)

    Glotch, Timothy D.; Bandfield, Joshua L.; Wolff, Michael J.; Arnold, Jessica A.; Che, Congcong

    2016-03-01

    Chloride salt-bearing deposits on Mars were discovered using the Mars Odyssey Thermal Emission Imaging System (THEMIS) and have been characterized by both mid-infrared (MIR) and visible-to-near-infrared (VNIR) remote sensing instruments. The chloride salt-bearing deposits exhibit a blue slope at MIR wavelengths and a featureless red slope at VNIR wavelengths. These deposits also lack strong 3 µm bands in VNIR spectra, indicating that they are desiccated compared to the surrounding regolith. The lack of VNIR spectral features suggests that an anhydrous chloride salt, the most likely of which is halite, is responsible for the observed spectral slope. In this work, we use laboratory spectra and a hybrid T-matrix/Hapke light scattering model to constrain the particle sizes and salt abundances of the Martian chloride salt-bearing deposits. Our work shows that the two broad spectral classes of these deposits observed by THEMIS can be explained by a difference in the particle size of the admixed silicate regolith. In all cases, chloride salt abundances of 10-25% are required to match the THEMIS data. The chloride salt abundances determined in this work suggest deposition in a lacustrine/playa setting or in association with late-stage groundwater upwelling.

  20. RESULTS FROM THE MOUNTAIN ACID DEPOSITION PROGRAM

    EPA Science Inventory

    The Mountain Acid Deposition Program (MADPro) was initiated in 1993 as part of the research necessary to support the objectives of the Clean Air Status and Trends Network (CASTNet), which was created to address the. requirements of the Clean Air Act Amendments (CAAA). The main ob...

  1. Preparation and characterization of ambazone salt with nicotinic acid

    NASA Astrophysics Data System (ADS)

    Kacsó, I.; Muresan-Pop, M.; Borodi, Gh.; Bratu, I.

    2012-02-01

    Salt formation is a good method of increasing solubility, dissolution rate and consequently the bioavailability of poor soluble acidic or basic drugs. The aim of this study was to obtain and to investigate the structural properties of the compound that was obtained by solvent drop grinding method at room temperature starting from the 1:1 molar ratios of ambazone (AMB) and nicotinic acid (NA). The obtained compound (AMB•NA) was investigated by thermal analysis (DSC, TG-DTA), X-ray powder diffraction (PXRD) and infrared spectroscopy (FTIR). The difference between the patterns of AMB•NA and of the starting compounds evidenced the formation of a salt. Using X-ray powder diffraction data, the lattice parameters were determined. The thermal and FTIR measurements on the pure compounds and on the (1:1) grinding mixture of AMB with NA confirm the salt formation.

  2. Methanol conversion over metal salts of 12-tungstophosphoric acid

    SciTech Connect

    Hayashi, H.; Moffat, J.B.

    1983-05-01

    The sodium, boron, calcium, magnesium, zinc, aluminum, and zirconium salts of 12-tungstophosphoric acid have been prepared and characterized using x-ray diffraction, mercury porosimetry, the chemisorption of ammonia, and Hammett indicators. Methanol conversion at 350/sup 0/C and a variety of residence times produced hydrocarbons ranging from C/sub 1/ to C/sub 5/ in amounts which varied with the cation. The more strongly acidic salts produced the higher yields of hydrocarbons. The maximum yield of the major product C/sub 4/ was found with the aluminum salt. The activities were related to the partial change on the oxygen atoms in the various catalysts. 3 figures, 1 table.

  3. Dilute acid/metal salt hydrolysis of lignocellulosics

    DOEpatents

    Nguyen, Quang A.; Tucker, Melvin P.

    2002-01-01

    A modified dilute acid method of hydrolyzing the cellulose and hemicellulose in lignocellulosic material under conditions to obtain higher overall fermentable sugar yields than is obtainable using dilute acid alone, comprising: impregnating a lignocellulosic feedstock with a mixture of an amount of aqueous solution of a dilute acid catalyst and a metal salt catalyst sufficient to provide higher overall fermentable sugar yields than is obtainable when hydrolyzing with dilute acid alone; loading the impregnated lignocellulosic feedstock into a reactor and heating for a sufficient period of time to hydrolyze substantially all of the hemicellulose and greater than 45% of the cellulose to water soluble sugars; and recovering the water soluble sugars.

  4. 77 FR 21676 - Silicic Acid, Sodium Salt etc.; Tolerance Exemption

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-04-11

    ...This regulation establishes an exemption from the requirement of a tolerance for residues of Silicic acid, sodium salt, reaction products with chlorotrimethylsilane and iso-propyl alcohol, reaction with poly(oxypropylene)-poly(oxyethylene) glycol; when used as an inert ingredient in a pesticide chemical formulation. Dow Corning Corporation submitted a petition to EPA under the Federal Food,......

  5. Oxalic acid, epsom salt and the poison bottle.

    PubMed

    Campbell, W A

    1982-03-01

    1 During the 19th century inadequate control of the sale of poisons, widespread illiteracy, and the English addiction to self-medication contributed to the high incidence of accidental poisoning by oxalic acid mistaken for Epsom salt. 2 Chemical methods for identifying oxalic acid failed when the product was adulterated. 3 Many mechanical devices were proposed to prevent careless dispensing; designs for poison bottles of distinctive shape, colour and texture appeared regularly for 40 years. PMID:6757103

  6. Acid deposition control benefits as problematic

    SciTech Connect

    Crocker, T.D.

    1985-01-01

    The author argues that the government's mistaken beliefs downgrade the benefits of acid deposition control, and may misdirect research of the effects of acid rain upon natural and human systems. It can be argued as to whether or not the factors (generally existing prices and yield changes from current standing stocks of environmental goods) upon which the $5 billion estimate for control was built have a major or minor influence upon the true economic consequences of acid deposition. As the application of Bayes' rule demonstrates, any lessening in arbitrariness of numerical assignments to the factors could lead to a major revision in the estimate. Assessment stories probably contribute to the paralysis of political will even though their truth value is small.

  7. CASTNet mountain acid deposition monitoring program

    SciTech Connect

    Bowser, J.J.; Anderson, J.B.; Edgerton, E.S.; Mohnen, V.; Baumgardener, R.

    1994-12-31

    Concern over the influence of air pollution on forest decline has led the USEPA to establish the Mountain Acid Deposition Monitoring Program (MADMP) to quantify total deposition at high altitudes, i.e., above cloud base. Clouds can be a major source of atmospheric deposition to sensitive, mountain ecosystems. This program is a part of the Clean Air Status and Trends Network (CASTNet), a national assessment of the effects of the 1990 Clean Air Act. The objectives of MADMP are to estimate total deposition, measure cloud chemistry, and characterize spacial and temporal trends at four selected high altitude sites in the Eastern US. Four MADMP sites have been established for the 1994 field season: Clingman`s Dome, Great Smoky Mountain Nat. Park, TN; Slide Mountain, Catskill State Park, NY; Whiteface Mountain, Adirondack State Park, NY; and Whitetop Mountain, Mt. Rogers Nat`l Recreational Area, VA. An automated cloud collection system will be utilized in combination with continuous measurements of cloud liquid water content in order to estimate cloudwater deposition. Other relevant data will include continuous meteorological measurements, ozone and sulfur dioxide concentrations, wet deposition from rainfall analysis, and dry deposition from filter pack analysis. Quality assurance and quality control measures will be employed to maximize accuracy and precision.

  8. Acidic deposition and surface water chemistry

    NASA Astrophysics Data System (ADS)

    Church, M. R.

    A pair of back-to-back (morning and afternoon) hydrology sessions, held December 10, 1987, at the AGU Fall Meeting in San Francisco, Calif., covered “Predicting the Effects of Acidic Deposition on Surface Water Chemistry.” The combined sessions included four invited papers, 12 contributed papers, and a panel discussion at its conclusion. The gathering dealt with questions on a variety of aspects of modeling the effects of acidic deposition on surface water chemistry.Contributed papers included discussions on the representation of processes in models as well as limiting assumptions in model application (V. S. Tripathi et al., Oak Ridge National Laboratory, Oak Ridge, Tenn., and E. C. Krug, Illinois State Water Survey, Champaign), along with problems in estimating depositional inputs to catchments and thus inputs to be used in the simulation of catchment response (M. M. Reddy et al., U.S. Geological Survey, Lakewood, Colo.; and E. A. McBean, University of Waterloo, Waterloo, Canada). L. A. Baker et al. (University of Minnesota, Minneapolis) dealt with the problem of modeling seepage lake systems, an exceedingly important portion of the aquatic resources in Florida and parts of the upper U.S. Midwest. J. A. Hau and Y. Eckstein (Kent State University, Kent, Ohio) considered equilibrium modeling of two northern Ohio watersheds that receive very different loads of acidic deposition but are highly similar in other respects.

  9. Acid deposition in Maryland: Implications of the results of the National Acid Precipitation Assessment Program

    SciTech Connect

    DeMuro, J.; Bowmann, M.; Ross, J.; Blundell, C.; Price, R.

    1991-07-01

    Acid deposition, commonly referred to as 'acid rain,' is a major global environmental concern. Acid deposition has reportedly resulted in damage to aquatic, terrestrial, and physical resources and has potentially adverse effects on human health. A component of the Maryland acid deposition program is the preparation of an annual report that summarizes yearly activities and costs of ongoing acid deposition research and monitoring programs.

  10. 40 CFR 721.6200 - Fatty acid polyamine condensate, phosphoric acid ester salts.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Fatty acid polyamine condensate, phosphoric acid ester salts. 721.6200 Section 721.6200 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.6200 Fatty acid polyamine condensate, phosphoric...

  11. 40 CFR 721.6200 - Fatty acid polyamine condensate, phosphoric acid ester salts.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Fatty acid polyamine condensate, phosphoric acid ester salts. 721.6200 Section 721.6200 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.6200 Fatty acid polyamine condensate, phosphoric...

  12. 40 CFR 721.6200 - Fatty acid polyamine condensate, phosphoric acid ester salts.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Fatty acid polyamine condensate, phosphoric acid ester salts. 721.6200 Section 721.6200 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.6200 Fatty acid polyamine condensate, phosphoric...

  13. 40 CFR 721.6200 - Fatty acid polyamine condensate, phosphoric acid ester salts.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Fatty acid polyamine condensate, phosphoric acid ester salts. 721.6200 Section 721.6200 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.6200 Fatty acid polyamine condensate, phosphoric...

  14. 40 CFR 721.6200 - Fatty acid polyamine condensate, phosphoric acid ester salts.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Fatty acid polyamine condensate, phosphoric acid ester salts. 721.6200 Section 721.6200 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.6200 Fatty acid polyamine condensate, phosphoric...

  15. (Acidic deposition: Its nature and impacts)

    SciTech Connect

    Cook, R.B.; Turner, R.S. ); Ryan, P.F. )

    1990-10-18

    The travelers presented papers on various aspects of modeling performed as part of the US National Acidic Precipitation Assessment Program (NAPAP) at the Fourth International Conference on Acidic Deposition: Its Nature and Impacts. The meeting was sponsored by the Royal Society of Edinburgh and was attended by over 800 scientists, primarily from Europe and North America. The conference focused on nine aspects of the nature and impacts of atmospheric pollutants, including ozone: chemistry of atmospheric pollutants; processes controlling the deposition of pollutants; effects of pollutants on soils; physiology of plant responses to pollutants; effects of pollutants in agricultural and natural or seminatural ecosystems; atmospheric pollutants and forests; effects of pollutants on the chemistry of freshwater streams and lakes; effects of pollutants on freshwater plants and animals; and effects of pollutants, indoors and outdoors, on materials and buildings.

  16. Potential for preservation of halobacteria and their macromolecular constituents in brine inclusions from bedded salt deposits

    NASA Astrophysics Data System (ADS)

    Fredrickson, James K.; Chandler, Darrell P.; Onstott, Tullis C.

    1997-07-01

    Halobacteria cultured from salt deposits as old as 200 m.y. are assumed to be dormant halobacteria entombed in the brine inclusions that formed during deposition of the salt crystals. Hypersaline lakes may have also existed on early Mars. If so, evaporite minerals containing frozen brine inclusions may occur on the surface of Mars today. Analyses of samples of recently-deposited salt from Laguna Grande de la Sal in New Mexico revealed the presence of viable halobacteria. 16S rDNA from archae and eubacteria was also detected by polymerase chain reaction (PCR) amplification of directly-extracted DNA from Laguna Grande de la Sal sal. In contrast, no halophilic bacteria were cultured from 200 my polyhalite from the Salado Formation in New Mexico nor was archaea 16S rDNA detected by PCR amplification of DNA extracts from salt. A combination of microbiological, molecular, and geochemical approaches are being used to probe bedded salt deposits for evidence of microbial entrapment in primary fluid inclusions. A chronosequence of bedded salts from Death Valley, California that range in age from 0 to 200 kyr is the subject of current investigations to constrain the length of time that viable halophilic bacteria and associated macromolecules can be detected in bedded salts.

  17. Acidic Depositions: Effects on Wildlife and Habitats

    USGS Publications Warehouse

    1993-01-01

    The phenomenon of 'acid rain' is not new; it was recognized in the mid-1800s in industrialized Europe. In the 1960s a synthesis of information about acidification began in Europe, along with predictions of ecological effects. In the U.S. studies of acidification began in the 1920s. By the late 1970s research efforts in the U.S. and Canada were better coordinated and in 1980 a 10-year research program was undertaken through the National Acid Precipitation Assessment Plan (NAPAP) to determine the causes and consequences of acidic depositions. Much of the bedrock in the northeastern U.S. and Canada contains total alkalinity of 20 kg/ha/yr of wet sulphate depositions and are vulnerable to acidifying processes. Acidic depositions contribute directly to acidifying processes of soil and soil water. Soils must have sufficient acid-neutralizing capacity or acidity of soil will increase. Natural soil-forming processes that lead to acidification can be accelerated by acidic depositions. Long-term effects of acidification are predicted, which will reduce soil productivity mainly through reduced availability of nutrients and mobilization of toxic metals. Severe effects may lead to major alteration of soil chemistry, soil biota, and even loss of vegetation. Several species of earthworms and several other taxa of soil-inhabiting invertebrates, which are important food of many vertebrate wildlife species, are affected by low pH in soil. Loss of canopy in declining sugar maples results in loss of insects fed on by certain neotropical migrant bird species. No definitive studies categorically link atmospheric acidic depositions with direct or indirect effects on wild mammals. Researchers have concentrated on vegetative and aquatic effects. Circumstantial evidence suggests that effects are probable for certain species of aquatic-dependent mammals (water shrew, mink, and otter) and that these species are at risk from the loss of foods or contamination of these foods by metals

  18. 40 CFR 721.3625 - Fatty acid amine salt (generic name).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Fatty acid amine salt (generic name... Substances § 721.3625 Fatty acid amine salt (generic name). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as fatty acid amine salt (PMN...

  19. 40 CFR 721.3625 - Fatty acid amine salt (generic name).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Fatty acid amine salt (generic name... Substances § 721.3625 Fatty acid amine salt (generic name). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as fatty acid amine salt (PMN...

  20. 40 CFR 721.5465 - Amine salt of organic acid (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Amine salt of organic acid (generic... Substances § 721.5465 Amine salt of organic acid (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as amine salt of organic acid...

  1. 40 CFR 721.5465 - Amine salt of organic acid (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Amine salt of organic acid (generic... Substances § 721.5465 Amine salt of organic acid (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as amine salt of organic acid...

  2. 40 CFR 721.3032 - Boric acid (H3BO2), zinc salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Boric acid (H3BO2), zinc salt. 721... Substances § 721.3032 Boric acid (H3BO2), zinc salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as boric acid (H3BO2), zinc salt (PMN...

  3. 40 CFR 721.3032 - Boric acid (H3BO2), zinc salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Boric acid (H3BO2), zinc salt. 721... Substances § 721.3032 Boric acid (H3BO2), zinc salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as boric acid (H3BO2), zinc salt (PMN...

  4. 40 CFR 721.3032 - Boric acid (H3BO2), zinc salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Boric acid (H3BO2), zinc salt. 721... Substances § 721.3032 Boric acid (H3BO2), zinc salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as boric acid (H3BO2), zinc salt (PMN...

  5. 40 CFR 721.3032 - Boric acid (H3BO2), zinc salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Boric acid (H3BO2), zinc salt. 721... Substances § 721.3032 Boric acid (H3BO2), zinc salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as boric acid (H3BO2), zinc salt (PMN...

  6. 40 CFR 721.3032 - Boric acid (H3BO2), zinc salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Boric acid (H3BO2), zinc salt. 721... Substances § 721.3032 Boric acid (H3BO2), zinc salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as boric acid (H3BO2), zinc salt (PMN...

  7. 40 CFR 721.10550 - Rare earth salt of a carboxylic acid (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Rare earth salt of a carboxylic acid... Specific Chemical Substances § 721.10550 Rare earth salt of a carboxylic acid (generic). (a) Chemical... as rare earth salt of a carboxylic acid (PMN P-05-324) is subject to reporting under this section...

  8. 40 CFR 721.10550 - Rare earth salt of a carboxylic acid (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Rare earth salt of a carboxylic acid... Specific Chemical Substances § 721.10550 Rare earth salt of a carboxylic acid (generic). (a) Chemical... as rare earth salt of a carboxylic acid (PMN P-05-324) is subject to reporting under this section...

  9. 40 CFR 721.9640 - Salt of an acrylic acid - acrylamide terpolymer (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Salt of an acrylic acid - acrylamide... Specific Chemical Substances § 721.9640 Salt of an acrylic acid - acrylamide terpolymer (generic). (a... generically as salt of an acrylic acid - acrylamide terpolymer (PMN P-99-817) is subject to reporting...

  10. 40 CFR 721.9640 - Salt of an acrylic acid - acrylamide terpolymer (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Salt of an acrylic acid - acrylamide... Specific Chemical Substances § 721.9640 Salt of an acrylic acid - acrylamide terpolymer (generic). (a... generically as salt of an acrylic acid - acrylamide terpolymer (PMN P-99-817) is subject to reporting...

  11. 40 CFR 721.9640 - Salt of an acrylic acid - acrylamide terpolymer (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Salt of an acrylic acid - acrylamide... Specific Chemical Substances § 721.9640 Salt of an acrylic acid - acrylamide terpolymer (generic). (a... generically as salt of an acrylic acid - acrylamide terpolymer (PMN P-99-817) is subject to reporting...

  12. 40 CFR 721.9640 - Salt of an acrylic acid - acrylamide terpolymer (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Salt of an acrylic acid - acrylamide... Specific Chemical Substances § 721.9640 Salt of an acrylic acid - acrylamide terpolymer (generic). (a... generically as salt of an acrylic acid - acrylamide terpolymer (PMN P-99-817) is subject to reporting...

  13. 40 CFR 721.9640 - Salt of an acrylic acid - acrylamide terpolymer (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Salt of an acrylic acid - acrylamide... Specific Chemical Substances § 721.9640 Salt of an acrylic acid - acrylamide terpolymer (generic). (a... generically as salt of an acrylic acid - acrylamide terpolymer (PMN P-99-817) is subject to reporting...

  14. 40 CFR 721.6110 - Alkyldi(alkyloxyhydroxypropyl) derivative, phosphoric acid esters, potassium salts.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...) derivative, phosphoric acid esters, potassium salts. 721.6110 Section 721.6110 Protection of Environment...) derivative, phosphoric acid esters, potassium salts. (a) Chemical substance and significant new uses subject...) derivative, phosphoric acid esters, potassium salts (PMN P-91-818) is subject to reporting under this...

  15. 40 CFR 721.6110 - Alkyldi(alkyloxyhydroxypropyl) derivative, phosphoric acid esters, potassium salts.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...) derivative, phosphoric acid esters, potassium salts. 721.6110 Section 721.6110 Protection of Environment...) derivative, phosphoric acid esters, potassium salts. (a) Chemical substance and significant new uses subject...) derivative, phosphoric acid esters, potassium salts (PMN P-91-818) is subject to reporting under this...

  16. 40 CFR 721.6110 - Alkyldi(alkyloxyhydroxypropyl) derivative, phosphoric acid esters, potassium salts.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...) derivative, phosphoric acid esters, potassium salts. 721.6110 Section 721.6110 Protection of Environment...) derivative, phosphoric acid esters, potassium salts. (a) Chemical substance and significant new uses subject...) derivative, phosphoric acid esters, potassium salts (PMN P-91-818) is subject to reporting under this...

  17. 21 CFR 172.725 - Gibberellic acid and its potassium salt.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Gibberellic acid and its potassium salt. 172.725... Additives § 172.725 Gibberellic acid and its potassium salt. The food additives gibberellic acid and its potassium salt may be used in the malting of barley in accordance with the following prescribed...

  18. 21 CFR 172.725 - Gibberellic acid and its potassium salt.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Gibberellic acid and its potassium salt. 172.725... HUMAN CONSUMPTION Other Specific Usage Additives § 172.725 Gibberellic acid and its potassium salt. The food additives gibberellic acid and its potassium salt may be used in the malting of barley...

  19. 21 CFR 172.725 - Gibberellic acid and its potassium salt.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Gibberellic acid and its potassium salt. 172.725... HUMAN CONSUMPTION Other Specific Usage Additives § 172.725 Gibberellic acid and its potassium salt. The food additives gibberellic acid and its potassium salt may be used in the malting of barley...

  20. 40 CFR 721.6110 - Alkyldi(alkyloxyhydroxypropyl) derivative, phosphoric acid esters, potassium salts.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...) derivative, phosphoric acid esters, potassium salts. 721.6110 Section 721.6110 Protection of Environment...) derivative, phosphoric acid esters, potassium salts. (a) Chemical substance and significant new uses subject...) derivative, phosphoric acid esters, potassium salts (PMN P-91-818) is subject to reporting under this...

  1. 40 CFR 721.6110 - Alkyldi(alkyloxyhydroxypropyl) derivative, phosphoric acid esters, potassium salts.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...) derivative, phosphoric acid esters, potassium salts. 721.6110 Section 721.6110 Protection of Environment...) derivative, phosphoric acid esters, potassium salts. (a) Chemical substance and significant new uses subject...) derivative, phosphoric acid esters, potassium salts (PMN P-91-818) is subject to reporting under this...

  2. 21 CFR 172.725 - Gibberellic acid and its potassium salt.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Gibberellic acid and its potassium salt. 172.725... HUMAN CONSUMPTION Other Specific Usage Additives § 172.725 Gibberellic acid and its potassium salt. The food additives gibberellic acid and its potassium salt may be used in the malting of barley...

  3. 21 CFR 172.725 - Gibberellic acid and its potassium salt.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Gibberellic acid and its potassium salt. 172.725... HUMAN CONSUMPTION Other Specific Usage Additives § 172.725 Gibberellic acid and its potassium salt. The food additives gibberellic acid and its potassium salt may be used in the malting of barley...

  4. 40 CFR 721.980 - Sodium salt of azo acid dye.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Sodium salt of azo acid dye. 721.980... Substances § 721.980 Sodium salt of azo acid dye. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a sodium salt of azo acid dye (PMN...

  5. 40 CFR 721.3625 - Fatty acid amine salt (generic name).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Fatty acid amine salt (generic name... Substances § 721.3625 Fatty acid amine salt (generic name). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as fatty acid amine salt (PMN...

  6. 40 CFR 721.980 - Sodium salt of azo acid dye.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Sodium salt of azo acid dye. 721.980... Substances § 721.980 Sodium salt of azo acid dye. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a sodium salt of azo acid dye (PMN...

  7. 40 CFR 721.5465 - Amine salt of organic acid (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Amine salt of organic acid (generic... Substances § 721.5465 Amine salt of organic acid (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as amine salt of organic acid...

  8. 40 CFR 721.3625 - Fatty acid amine salt (generic name).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Fatty acid amine salt (generic name... Substances § 721.3625 Fatty acid amine salt (generic name). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as fatty acid amine salt (PMN...

  9. 40 CFR 721.5465 - Amine salt of organic acid (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Amine salt of organic acid (generic... Substances § 721.5465 Amine salt of organic acid (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as amine salt of organic acid...

  10. 40 CFR 721.980 - Sodium salt of azo acid dye.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Sodium salt of azo acid dye. 721.980... Substances § 721.980 Sodium salt of azo acid dye. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a sodium salt of azo acid dye (PMN...

  11. 40 CFR 721.3625 - Fatty acid amine salt (generic name).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Fatty acid amine salt (generic name... Substances § 721.3625 Fatty acid amine salt (generic name). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as fatty acid amine salt (PMN...

  12. 40 CFR 721.980 - Sodium salt of azo acid dye.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Sodium salt of azo acid dye. 721.980... Substances § 721.980 Sodium salt of azo acid dye. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a sodium salt of azo acid dye (PMN...

  13. 40 CFR 721.980 - Sodium salt of azo acid dye.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Sodium salt of azo acid dye. 721.980... Substances § 721.980 Sodium salt of azo acid dye. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a sodium salt of azo acid dye (PMN...

  14. 40 CFR 721.5465 - Amine salt of organic acid (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Amine salt of organic acid (generic... Substances § 721.5465 Amine salt of organic acid (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as amine salt of organic acid...

  15. 40 CFR 721.10568 - Diethanolamine salt of polymeric acid (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Diethanolamine salt of polymeric acid... Specific Chemical Substances § 721.10568 Diethanolamine salt of polymeric acid (generic). (a) Chemical... as diethanolamine salt of polymeric acid (PMN P-08-464) is subject to reporting under this...

  16. 40 CFR 721.10568 - Diethanolamine salt of polymeric acid (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Diethanolamine salt of polymeric acid... Specific Chemical Substances § 721.10568 Diethanolamine salt of polymeric acid (generic). (a) Chemical... as diethanolamine salt of polymeric acid (PMN P-08-464) is subject to reporting under this...

  17. Depositional patterns and structural styles-Hackberry Salt Dome, Cameron Parish, Louisiana

    SciTech Connect

    Spencer, J.A.; Sharpe, C.L.; Gillham, T.H.; Wright, D.N.

    1994-12-31

    The West and East Hackberry fields of north-central Cameron Parish, Louisiana, are associated with a large southeast-plunging salt ridge. Episodes of salt movement influenced the depositional patterns and reservoir trap styles of the Oligocene- and Miocene-age sedimentary section. The Oligocene lower Hackberry channels were influenced by the salt structure, resulting in the Manchester-Holmwood channel system flanking the east and south sides of the salt dome and the Choupique channel system flanking the west side of the salt dome. The depositional patterns and structural bed dips of the younger Oligocene Camerina A to marginulina section demonstrate a major period of salt movement and erosion. The resulting truncation of the Camerian A sandstones, sealed by overlying shales, provides the dominant trap style for the majority of the reservoirs. This same general period of salt movement influenced the orientation of the Oligocene Marginulina to Miogypsinoides expansion fault system to the east. The Sweet Lake salt dome, down through to this expansion system, probably represents a southeast extension of this ancestral salt ridge.

  18. Depositional patterns and structural styles - Hackberry Salt Dome, Cameron Parish, Louisiana

    SciTech Connect

    Spencer, J.A.; Sharpe, C.L.; Gillham, T.H.

    1994-09-01

    The west and east Hackberry fields of north-central Cameron Parish, Louisiana, are associated with a large southeast-plunging salt ridge. Episodes of salt movement influenced the depositional patterns and reservoir trap styles of the Oligocene and Miocene age section. The Oligocene lower Hackberry channels were influenced by the salt, resulting in the {open_quotes}Manchester-Holmwood{close_quotes} channel system skirting the east and south flanks of the salt and the {open_quotes}Choupique{close_quotes} channel system skirting the west flank of the salt. The depositional patterns and structural bed dips of the younger Oligocene Camerina (A) to Marginulina section demonstrate a major period of salt movement and erosion. The resulting truncation of the Camerina (A) sands, sealed by overlying shales, provides the dominant trap style for the majority of the fields` reservoirs. This same general period of salt movement influenced the orientation of the Oligocene Camerina (A) - Miogypsinoides expansion fault systems of the prolific Miogypsinoides embayment. The Sweet Lake salt dome, downthrown to this expansion system, probably represents a southeast extension of this ancestral salt ridge.

  19. Geobiological Assessment of Evaporite Deposits in the Great Salt Lake Desert: Preliminary Results

    NASA Astrophysics Data System (ADS)

    Lynch, K.; Zabrusky, K.; Lossing, R.; Hoehler, T. M.; Spear, J. R.

    2010-12-01

    The study of analog evaporitic environments on Earth is of increasing importance due to the multiple reports of possible evaporite deposits across the martian surface. If life ever evolved on the red planet, these deposits could have harbored potential energy sources and preserved microfossils. Evaporite deposits on earth are often associated with preserved organic material, and understanding the relationships of evaporites and organics will be important for such detections on Mars. Additionally, naturally occurring perchlorate deposits are typically associated with evaporitic materials and further understanding of geobiological processes of this oxidant will be of great use for future habitability assessments on Mars. In order to fully evaluate the astrobiological potential of martian evaporites, a wide variety of terrestrial analog systems can be studied. One understudied system is the Great Salt Lake Desert and its associated features. The Great Salt Lake Desert is the remnant bed of ancient Lake Bonneville, one of the several giant lakes from the Pleistocene Epoch and covered about 20,000 square miles of western Utah and smaller sections of eastern Nevada and southern Idaho. The most well know remnant lake features are the Bonneville Salt Flats and the Great Salt Lake. The Bonneville Salt Flats represent a mainly closed system that receives little to no recharge. The Great Salt Lake, however, still has fresh water recharge its southern arm. The mineralogy of both systems is dominated by halite. The salt flats also have deposits of gypsum, potassium chloride, and a host of magnesium, potassium, and sodium salts. Although the Great Salt Lake Desert has high economic importance, the geobiological potential of its evaporitic features has rarely been studied and there is little to no information regarding the microbial diversity within some of the richest deposits. Here we present the preliminary results of a geobiological study of a sample transect that stretches

  20. Emerging acid deposition research and monitoring issues

    SciTech Connect

    Birnbaum, R.

    1997-12-31

    The research baselines established for acid rain in the 1980s position scientists and policy makers to evaluate the environmental effectiveness of the acid rain control program and to test the variety of scientific hypotheses made regarding the chemical, transport and biological processes involved in acidic deposition. Several new research questions have evolved. How effective are the emissions reductions? What is the residual risk? How have ecological recovery rates been affected and what other environmental factors influence recovery? What are the critical requirements to measure ecological change including the extent and rate while also capturing the extent and severity of emerging ecological stressors (such as watershed nitrogen saturation)? These and other questions are currently being synthesized within and outside of EPA to develop a long-term strategy to provide guidance to emerging research and monitoring issues.

  1. Salt deposits in Los Medanos area, Eddy and Lea counties, New Mexico

    USGS Publications Warehouse

    Jones, C.L.; with sections on Ground water hydrology, Cooley, Maurice E.; and Surficial Geology, Bachman, George Odell

    1973-01-01

    The salt deposits of Los Medanos area, in Eddy and Lea Counties, southeastern New Mexico, are being considered for possible use as a receptacle for radioactive wastes in a pilot-plant repository. The salt deposits of the area. are in three evaporite formations: the Castile, Salado, and Rustler Formations, in ascending order. The three formations are dominantly anhydrite and rock salt, but some gypsum, potassium ores, carbonate rock, and fine-grained clastic rocks are present. They have combined thicknesses of slightly more than 4,000 feet, of which roughly one-half belongs to the Salado. Both the Castile and the Rustler are-richer in anhydrite-and poorer in rock salt-than the Salado, and they provide this salt-rich formation with considerable Protection from any fluids which might be present in underlying or overlying rocks. The Salado Formation contains many thick seams of rock salt at moderate depths below the surface. The rock salt has a substantial cover of well-consolidated rocks, and it is very little deformed structurally. Certain geological details essential for Waste-storage purposes are unknown or poorly known, and additional study involving drilling is required to identify seams of rock salt suitable for storage purposes and to establish critical details of their chemistry, stratigraphy, and structure.

  2. Palmitoleic acid calcium salt: a lubricant and bactericidal powder from natural lipids.

    PubMed

    Yamamoto, Yoshiaki; Kawamura, Yuki; Yamazaki, Yuki; Kijima, Tatsuro; Morikawa, Toshiya; Nonomura, Yoshimune

    2015-01-01

    Palmitoleic acid is a promising bactericidal agent for cleansing products with alternative bactericidal abilities. In this study, we focus on the physical and biological activity of palmitoleic acid calcium salt (C16:1 fatty acid Ca salt) because it forms via an ion-exchange reaction between palmitoleic acid and Ca ions in tap water, and remains on the skin surface during the cleansing process. Here, we prepared C16:1 fatty acid Ca salt to investigate its crystal structure and physical and bactericidal properties. The Ca salt was a plate-shaped lamellar crystalline powder with a particle diameter of several micrometers to several tens of micrometers; it exhibited significant lubricity and alternative bactericidal activity against Staphylococcus aureus (S. aureus) and Propionibacterium acnes (P. acnes). We also examined other fatty acid Ca salts prepared from lauric acid (C12:0 fatty acid), palmitic acid (C16:0 fatty acid), and oleic acid (C18:1 fatty acid). The bactericidal activities and lubricity of the fatty acid Ca salts changed with the alkyl chain length and the degree of unsaturation. The C16:1 fatty acid Ca salt exhibited the strongest selective bactericidal ability among the four investigated fatty acid Ca salts. These findings suggest that C16:1 fatty acid and its Ca salt have potential applications in cleansing and cosmetic products. PMID:25757432

  3. Synthesis of an acid addition salt of delta-aminolevulinic acid from 5-bromo levulinic acid esters

    DOEpatents

    Moens, L.

    1999-05-25

    A process is disclosed for preparing an acid addition salt of delta-aminolevulinic acid comprising. The process involves dissolving a lower alkyl 5-bromolevulinate and an alkali metal diformylamide in an organic solvent selected from the group consisting of acetonitrile, methanol, tetrahydrofuran, 2-methyltetrahydrofuran and methylformate or mixtures to form a suspension of an alkyl 5-(N,N-diformylamino) levulinate ester; and hydrolyzing the alkyl 5-(N,N-diformylamino) levulinate with an inorganic acid to form an acid addition salt of delta-amino levulinic acid.

  4. Synthesis of an acid addition salt of delta-aminolevulinic acid from 5-bromo levulinic acid esters

    DOEpatents

    Moens, Luc

    1999-01-01

    A process of preparing an acid addition salt of delta-aminolevulinic acid comprising: dissolving a lower alkyl 5-bromolevulinate and an alkali metal diformylamide in an organic solvent selected from the group consisting of acetonitrile, methanol, tetrahydrofuran, 2-methyltetrahydrofuran and methylformate or mixtures thereof to form a suspension of an alkyl 5-(N,N-diformylamino) levulinate ester; and hydrolyzing said alkyl 5-(N,N-diformylamino) levulinate with an inorganic acid to form an acid addition salt of delta-amino levulinic acid.

  5. The Composition and Physical Properties of Chloride Salt-bearing Deposits on Mars

    NASA Astrophysics Data System (ADS)

    Glotch, T. D.; Bandfield, J.; Wolff, M. J.; Arnold, J. A.; Che, C.

    2015-12-01

    Anhydrous chloride salt deposits were first discovered on Mars by the 2001 Odyssey Thermal Emission Imaging System (THEMIS) and have been further characterized by Mars Reconnaissance Orbiter CRISM and Mars Express visible/near-IR (VNIR) hyperspectral imaging spectrometers. At mid-IR wavelengths, the salt-bearing deposits display a blue slope superimposed on the regional regolith spectral shape. At VNIR wavelengths, ratio spectra display a featureless red slope between 1.0 and 2.5 μm and a reduced 3 μm band, indicating that the deposits are desiccated compared to the surrounding terrain. In this work, we compare laboratory and model spectra to THEMIS spectra to evaluate the abundance and physical properties of salt in these deposits. We acquired mid-IR emissivity spectra of a suite of halite/basalt mixtures separated to <10 μm, 63-90 μm, 125-180 μm, and 250-355 μm. Halite concentrations for each size separate ranged from 1-75%. Laboratory spectra of the coarsest particulates do not adequately reproduce the spectral shapes associated with any of the Martian salt deposits. The finest particulates display spectral characteristics associated with salt deposits found in high albedo, dusty regions of Mars, and those in the middle size ranges are consistent with the spectra of most Martian salt deposits and suggest abundances between 10 and 25 wt.% salt. The increase in salt content from ~10-25% coincides with a shift in the THEMIS emissivity maximum from band 3 to band 4, suggesting this can be used as a rough indicator of salt content in remote sensing studies. We also used a hybrid T-matrix/Hapke light scattering model to model the scattering properties and mid-IR spectra of clusters of salt/silicate spheres. The model results show that as halite content is increased, the transparency of the cluster increases substantially, resulting in multiple internal scattering, and substantially reduced emissivity, consistent with the THEMIS data and laboratory spectra. Phase

  6. Ancillary effects of selected acid deposition control policies

    SciTech Connect

    Moe, R.J.; Lyke, A.J.; Nesse, R.J.

    1986-08-01

    NAPAP is examining a number of potential ways to reduce the precursors (sulfur dioxide and nitrogen oxides) to acid deposition. However, the policies to reduce acid deposition will have other physical, biological and economic effects unrelated to acid deposition. For example, control policies that reduce sulfur dioxide emissions may also increase visibility. The effects of an acid deposition policy that are unrelated to acid deposition are referred to as ''ancillary'' effects. This reserch identifies and characterizes the principle physical and economic ancillary effects associated with acid deposition control and mitigation policies. In this study the ancillary benefits associated with four specific acid deposition policy options were investigated. The four policy options investigated are: (1) flue gas desulfurization, (2) coal blending or switching, (3) reductions in automobile emissions of NO/sub x/, and (4) lake liming. Potential ancillary benefits of each option were identified and characterized. Particular attention was paid to the literature on economic valuation of potential ancillary effects.

  7. Localized chrysiasis, aluminum salt deposition and dystrophic calcification a decade after gold injections.

    PubMed

    Gowring, Lena E; Kobayashi, Todd T; Lewin-Smith, Michael R

    2015-08-01

    Localized chrysiasis is rare and can occur in two settings: after localized or traumatic implantation of elemental gold or gold salts or after localized laser or light therapy in someone who has been previously exposed to systemic gold therapy. We report a unique case of localized chrysiasis with associated aluminum salt deposition and sclerosing lipogranulomas because of previous injections of aurothioglucose (Solganal®). The unique histopathologic findings seen in this case have not been previously reported. PMID:25950356

  8. 40 CFR 721.4663 - Fluorinated carboxylic acid alkali metal salts.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... metal salts. 721.4663 Section 721.4663 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.4663 Fluorinated carboxylic acid alkali metal salts. (a) Chemical... fluorinated carboxylic acid alkali metal salts (PMNs P-95-979/980/981) are subject to reporting under...

  9. Students' Understanding of Acid, Base and Salt Reactions in Qualitative Analysis.

    ERIC Educational Resources Information Center

    Tan, Kim-Chwee Daniel; Goh, Ngoh-Khang; Chia, Lian-Sai; Treagust, David F.

    2003-01-01

    Uses a two-tier, multiple-choice diagnostic instrument to determine (n=915) grade 10 students' understanding of the acid, base, and salt reactions involved in basic qualitative analysis. Reports that many students did not understand the formation of precipitates and the complex salts, acid/salt-base reactions, and thermal decomposition involved in…

  10. 40 CFR 721.10487 - Alkylbenzenes sulfonic acids, metal salts (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... salts (generic). 721.10487 Section 721.10487 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.10487 Alkylbenzenes sulfonic acids, metal salts (generic). (a) Chemical... as alkylbenzenes sulfonic acids, metal salts (PMNs P-04-599, P-04-600, P-04-605, and P-04-606)...

  11. 40 CFR 721.10382 - Diphosphoric acid, calcium salt (1:1).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Diphosphoric acid, calcium salt (1:1... Specific Chemical Substances § 721.10382 Diphosphoric acid, calcium salt (1:1). (a) Chemical substance and... salt (1:1) (PMN P-10-313; CAS No. 14866-19-4) is subject to reporting under this section for...

  12. 40 CFR 721.4663 - Fluorinated carboxylic acid alkali metal salts.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... metal salts. 721.4663 Section 721.4663 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.4663 Fluorinated carboxylic acid alkali metal salts. (a) Chemical... fluorinated carboxylic acid alkali metal salts (PMNs P-95-979/980/981) are subject to reporting under...

  13. 40 CFR 721.10098 - Disubstituted benzoic acid, alkali metal salt (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... metal salt (generic). 721.10098 Section 721.10098 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.10098 Disubstituted benzoic acid, alkali metal salt... identified generically as disubstituted benzoic acid, alkali metal salt (PMN P-03-643) is subject...

  14. 40 CFR 721.10382 - Diphosphoric acid, calcium salt (1:1).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Diphosphoric acid, calcium salt (1:1... Specific Chemical Substances § 721.10382 Diphosphoric acid, calcium salt (1:1). (a) Chemical substance and... salt (1:1) (PMN P-10-313; CAS No. 14866-19-4) is subject to reporting under this section for...

  15. 40 CFR 721.2098 - Aliphatic polycarboxylic acid metal salt (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... salt (generic). 721.2098 Section 721.2098 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.2098 Aliphatic polycarboxylic acid metal salt (generic). (a) Chemical... as an aliphatic polycarboxylic acid metal salt (PMN P-01-7) is subject to reporting under...

  16. 40 CFR 721.10098 - Disubstituted benzoic acid, alkali metal salt (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... metal salt (generic). 721.10098 Section 721.10098 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.10098 Disubstituted benzoic acid, alkali metal salt... identified generically as disubstituted benzoic acid, alkali metal salt (PMN P-03-643) is subject...

  17. 40 CFR 721.2098 - Aliphatic polycarboxylic acid metal salt (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... salt (generic). 721.2098 Section 721.2098 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.2098 Aliphatic polycarboxylic acid metal salt (generic). (a) Chemical... as an aliphatic polycarboxylic acid metal salt (PMN P-01-7) is subject to reporting under...

  18. 40 CFR 721.10098 - Disubstituted benzoic acid, alkali metal salt (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... metal salt (generic). 721.10098 Section 721.10098 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.10098 Disubstituted benzoic acid, alkali metal salt... identified generically as disubstituted benzoic acid, alkali metal salt (PMN P-03-643) is subject...

  19. 40 CFR 721.4663 - Fluorinated carboxylic acid alkali metal salts.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... metal salts. 721.4663 Section 721.4663 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.4663 Fluorinated carboxylic acid alkali metal salts. (a) Chemical... fluorinated carboxylic acid alkali metal salts (PMNs P-95-979/980/981) are subject to reporting under...

  20. 40 CFR 721.10098 - Disubstituted benzoic acid, alkali metal salt (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... metal salt (generic). 721.10098 Section 721.10098 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.10098 Disubstituted benzoic acid, alkali metal salt... identified generically as disubstituted benzoic acid, alkali metal salt (PMN P-03-643) is subject...

  1. 40 CFR 721.4663 - Fluorinated carboxylic acid alkali metal salts.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... metal salts. 721.4663 Section 721.4663 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.4663 Fluorinated carboxylic acid alkali metal salts. (a) Chemical... fluorinated carboxylic acid alkali metal salts (PMNs P-95-979/980/981) are subject to reporting under...

  2. 40 CFR 721.720 - Alkoxylated fatty acid amide, alkylsulfate salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ..., alkylsulfate salt. 721.720 Section 721.720 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.720 Alkoxylated fatty acid amide, alkylsulfate salt. (a) Chemical... as an alkoxylated fatty acid amide, alkylsulfate salt (PMN P-97-136) is subject to reporting...

  3. 40 CFR 721.2098 - Aliphatic polycarboxylic acid metal salt (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... salt (generic). 721.2098 Section 721.2098 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.2098 Aliphatic polycarboxylic acid metal salt (generic). (a) Chemical... as an aliphatic polycarboxylic acid metal salt (PMN P-01-7) is subject to reporting under...

  4. 40 CFR 721.2098 - Aliphatic polycarboxylic acid metal salt (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... salt (generic). 721.2098 Section 721.2098 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.2098 Aliphatic polycarboxylic acid metal salt (generic). (a) Chemical... as an aliphatic polycarboxylic acid metal salt (PMN P-01-7) is subject to reporting under...

  5. 40 CFR 721.720 - Alkoxylated fatty acid amide, alkylsulfate salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ..., alkylsulfate salt. 721.720 Section 721.720 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.720 Alkoxylated fatty acid amide, alkylsulfate salt. (a) Chemical... as an alkoxylated fatty acid amide, alkylsulfate salt (PMN P-97-136) is subject to reporting...

  6. 40 CFR 721.720 - Alkoxylated fatty acid amide, alkylsulfate salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ..., alkylsulfate salt. 721.720 Section 721.720 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.720 Alkoxylated fatty acid amide, alkylsulfate salt. (a) Chemical... as an alkoxylated fatty acid amide, alkylsulfate salt (PMN P-97-136) is subject to reporting...

  7. 40 CFR 721.720 - Alkoxylated fatty acid amide, alkylsulfate salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ..., alkylsulfate salt. 721.720 Section 721.720 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.720 Alkoxylated fatty acid amide, alkylsulfate salt. (a) Chemical... as an alkoxylated fatty acid amide, alkylsulfate salt (PMN P-97-136) is subject to reporting...

  8. 40 CFR 721.720 - Alkoxylated fatty acid amide, alkylsulfate salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ..., alkylsulfate salt. 721.720 Section 721.720 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.720 Alkoxylated fatty acid amide, alkylsulfate salt. (a) Chemical... as an alkoxylated fatty acid amide, alkylsulfate salt (PMN P-97-136) is subject to reporting...

  9. 40 CFR 721.10382 - Diphosphoric acid, calcium salt (1:1).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Diphosphoric acid, calcium salt (1:1... Specific Chemical Substances § 721.10382 Diphosphoric acid, calcium salt (1:1). (a) Chemical substance and... salt (1:1) (PMN P-10-313; CAS No. 14866-19-4) is subject to reporting under this section for...

  10. Deposition of salicylic acid into hamster sebaceous.

    PubMed

    Motwani, M R; Rhein, L D; Zatz, J L

    2004-01-01

    In an earlier paper, we identified vehicles that are miscible with sebum, using differential scanning calorimetry (DSC). In this paper, the potential of these vehicles to deliver salicylic acid (SA) into the sebum-filled follicles of hamster ears is examined. The main objective of this study is to correlate the melting transitions of a model sebum with the follicular delivery of SA, using two different types of vehicles (fatty and polar). Generally, the fatty vehicles show higher deposition than the polar vehicles. Follicular delivery of salicylic acid correlates well with its solubility in the respective vehicles. This extent of deposition also shows a relationship with the effect of the vehicle on thermal behavior of the model sebum. The nature of the relationship depends on the vehicle (polar or fatty) tested. We conclude that DSC could be used to identify appropriate vehicles for drugs whose follicular delivery depends on solubility. The results also suggest that delivery into the sebaceous glands occurs by two different mechanisms, depending upon the polarity of the vehicle and the physicochemical properties of the drug. The results of these experiments are further extended to investigate follicular delivery of SA from two different types of oil-in-water emulsion formulations. From these studies we conclude that either increasing the volume of the oil phase or changing the emulsion to a water-in-oil emulsion would increase follicular deposition. Our research highlights the role of sebum, its compatibility with drug molecules, and vehicle selection in the transport of drugs into the follicles. The overall results of these experiments provide a reasonable understanding of the mechanisms underlying the transport of drugs to, and subsequently through, the sebaceous follicle. PMID:15645108

  11. 40 CFR 721.10097 - Disubstituted benzenesulfonic acid, alkali metal salt (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... PROTECTION AGENCY (CONTINUED) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES... metal salt (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as disubstituted benzenesulfonic acid, alkali metal salt (PMN...

  12. Workshop on Viability of Halophilic Bacteria in Salt Deposits

    NASA Technical Reports Server (NTRS)

    1997-01-01

    The significance of finding viable extreme halophiles in halites associated with Permian-aged sedimentary deposits is considered. Issues related to the microbiology and geochemistry of the halite environment are addressed. Recommendations that related the significance of this phenomenon to NASA's interest in planetary exploration and the early evolution of life are provided.

  13. STATUS OF RESEARCH TO DEVELOP ACIDIC DRY DEPOSITION MONITORING CAPABILITY

    EPA Science Inventory

    Dry deposition is thought to be as important as wet deposition in acidifying ecosystems. However, at present acidic dry deposition of relevant particles and gases cannot be monitored directly in a quantitative manner. The U.S. EPA Workshop on Dry Deposition (Report No. EPA-600/9-...

  14. Salt Profile in Sedimentary Deposits: an archive of past climate and tectonics

    NASA Astrophysics Data System (ADS)

    Sun, T.; Bao, H.; Reich, M.

    2013-12-01

    In hyper-arid environments, paleoclimatic and paleoenvironmental studies typically evaluate paleosol-based proxies such as morphology, variation of remnant vegetations, and geochemical and isotopic signatures of minerals to reveal the plaeoclimatic changes. Limited works utilized geochemical/isotopic approaches in sedimentary deposits which barely experience pedogenic processes. The objectives of this work are to evaluate the isotopic systematics and total chemistry of salts as function of depth within unsolidated sediments in an effort to reconstruct paleoclimatic conditions of Atacama Desert. Results of this work will demonstrate techniques that can also be applied in other hyper-arid environments (e.g., Antarctica, Mars). We report a study on a ~75 meter thick core from alluvial sedimentary deposits (Atacama Gravels) in the eastern margin of the central depression of Atacama desert, North Chile. This work combines mineralogical/geochemical/isotopic approaches to decipher the depositional conditions and the climatic conditions during and between sedimentation events. Our main focus is on the soluble sulfate, nitrate, chloride profiles through the sediments. These salt deposits likely originated from seasalts, atmospherically produced salts and/or salts from nearby evaporite deposits. The sources of salts are likely affected by offshore oceanic currents that may vary the seasalt input, or by regional tectonic or orogenic changes that may vary the terrestrial sources and their ratio with seasalt input. The outflux of the salts in these deposits are mainly due to groundwater drainage, and microbial facilitated salt consumption (e.g. sulfate reduction, denitrification), both of which are indicative of paleoclimatic conditions. Thus, the salt profile within the sediments records regional paleo-climate, global oceanic current setting, and regional tectonic activity. Morphological and mineralogical studies show that the target "gravel" consists of two main suites of

  15. Self-assembly of fatty acid-alkylboladiamine salts.

    PubMed

    Douliez, Jean-Paul; Navailles, Laurence; Nallet, Frédéric

    2006-01-17

    Long-chain fatty acids are insoluble in aqueous solution and form crystal precipitates. It is then of particular importance to determine the physicochemical parameters allowing their dispersion in water to improve their bioavailability and their utilization as surfactants. Herein, we report a study on salt-free catanionic systems in aqueous solution made of mixtures between palmitic or stearic fatty acids and alkylboladiamines (Abd's) differing by their alkyl chain length. Phase contrast microscopy, solid-state NMR, Fourier transform infrared spectroscopy, and small-angle neutron scattering were used to characterize the phase behavior of these systems at molar ratio of fatty acid to Abd of 1 and 2. Whatever the Abd and the molar ratio, fatty acids were embedded at low temperature in a bilayer gel phase which crystallizes after a period of rest. At an equimolar ratio, the gel phases transited upon raising the temperature to an isotropic phase made of worm-like micelles except in the case of the ethylenediamine chain for which a lamellar fluid phase was observed. At a molar ratio of 2 and high temperature, fatty acids were embedded in a lamellar fluid phase which self-orients with its stacking axis perpendicular to the magnetic field. However, for a long alkylboladiamine such as spermine, worm-like micelles formed. The phase behavior at high temperature is discussed in terms of molecular volume. PMID:16401110

  16. Alleviation of salt stress in lemongrass by salicylic acid.

    PubMed

    Idrees, Mohd; Naeem, M; Khan, M Nasir; Aftab, Tariq; Khan, M Masroor A; Moinuddin

    2012-07-01

    Soil salinity is one of the key factors adversely affecting the growth, yield, and quality of crops. A pot study was conducted to find out whether exogenous application of salicylic acid could ameliorate the adverse effect of salinity in lemongrass (Cymbopogon flexuosus Steud. Wats.). Two Cymbopogon varieties, Krishna and Neema, were used in the study. Three salinity levels, viz, 50, 100, and 150 mM of NaCl, were applied to 30-day-old plants. Salicylic acid (SA) was applied as foliar spray at 10(-5) M concentration. Totally, six SA-sprays were carried out at 10-day intervals, following the first spray at 30 days after sowing. The growth parameters were progressively reduced with the increase in salinity level; however, growth inhibition was significantly reduced by the foliar application of SA. With the increase in salt stress, a gradual decrease in the activities of carbonic anhydrase and nitrate reductase was observed in both the varieties. SA-treatment not only ameliorated the adverse effects of NaCl but also showed a significant improvement in the activities of these enzymes compared with the untreated stressed-plants. The plants supplemented with NaCl exhibited a significant increase in electrolyte leakage, proline content, and phosphoenol pyruvate carboxylase activity. Content and yield of essential oil was also significantly decreased in plants that received salinity levels; however, SA overcame the unfavorable effects of salinity stress to a considerable extent. Lemongrass variety Krishna was found to be more adapted to salt stress than Neema, as indicated by the overall performance of the two varieties under salt conditions. PMID:21882051

  17. 40 CFR 721.7785 - Substituted alkyl aminomethylene polyphosphonic acid, salt (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... polyphosphonic acid, salt (generic). 721.7785 Section 721.7785 Protection of Environment ENVIRONMENTAL PROTECTION... acid, salt (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a substituted alkylamino methylene polyphosphonic acid,...

  18. 40 CFR 721.7785 - Substituted alkyl aminomethylene polyphosphonic acid, salt (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... polyphosphonic acid, salt (generic). 721.7785 Section 721.7785 Protection of Environment ENVIRONMENTAL PROTECTION... acid, salt (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a substituted alkylamino methylene polyphosphonic acid,...

  19. 40 CFR 721.10487 - Alkylbenzenes sulfonic acids, metal salts (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Alkylbenzenes sulfonic acids, metal... Specific Chemical Substances § 721.10487 Alkylbenzenes sulfonic acids, metal salts (generic). (a) Chemical... as alkylbenzenes sulfonic acids, metal salts (PMNs P-04-599, P-04-600, P-04-605, and P-04-606)...

  20. 40 CFR 721.10474 - Substituted amino ethane sulfonic acid salt (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Substituted amino ethane sulfonic acid... Specific Chemical Substances § 721.10474 Substituted amino ethane sulfonic acid salt (generic). (a... generically as substituted amino ethane sulfonic acid salt (PMN P-04-107) is subject to reporting under...

  1. 40 CFR 721.10633 - Aromatic sulfonic acid amino azo dye salts (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Aromatic sulfonic acid amino azo dye... Specific Chemical Substances § 721.10633 Aromatic sulfonic acid amino azo dye salts (generic). (a) Chemical... as aromatic sulfonic acid amino azo dye salts (PMN P-12-276) is subject to reporting under...

  2. 40 CFR 721.10474 - Substituted amino ethane sulfonic acid salt (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Substituted amino ethane sulfonic acid... Specific Chemical Substances § 721.10474 Substituted amino ethane sulfonic acid salt (generic). (a... generically as substituted amino ethane sulfonic acid salt (PMN P-04-107) is subject to reporting under...

  3. 40 CFR 721.10633 - Aromatic sulfonic acid amino azo dye salts (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Aromatic sulfonic acid amino azo dye... Specific Chemical Substances § 721.10633 Aromatic sulfonic acid amino azo dye salts (generic). (a) Chemical... as aromatic sulfonic acid amino azo dye salts (PMN P-12-276) is subject to reporting under...

  4. 40 CFR 721.2175 - Salt of cyclodiamine and mineral acid.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Salt of cyclodiamine and mineral acid... Substances § 721.2175 Salt of cyclodiamine and mineral acid. (a) Chemical substance and significant new uses... mineral acid (PMN P-91-838) is subject to reporting under this section for the significant new...

  5. 40 CFR 721.2175 - Salt of cyclodiamine and mineral acid.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Salt of cyclodiamine and mineral acid... Substances § 721.2175 Salt of cyclodiamine and mineral acid. (a) Chemical substance and significant new uses... mineral acid (PMN P-91-838) is subject to reporting under this section for the significant new...

  6. 40 CFR 721.2175 - Salt of cyclodiamine and mineral acid.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Salt of cyclodiamine and mineral acid... Substances § 721.2175 Salt of cyclodiamine and mineral acid. (a) Chemical substance and significant new uses... mineral acid (PMN P-91-838) is subject to reporting under this section for the significant new...

  7. 40 CFR 721.2175 - Salt of cyclodiamine and mineral acid.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Salt of cyclodiamine and mineral acid... Substances § 721.2175 Salt of cyclodiamine and mineral acid. (a) Chemical substance and significant new uses... mineral acid (PMN P-91-838) is subject to reporting under this section for the significant new...

  8. 40 CFR 721.2175 - Salt of cyclodiamine and mineral acid.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Salt of cyclodiamine and mineral acid... Substances § 721.2175 Salt of cyclodiamine and mineral acid. (a) Chemical substance and significant new uses... mineral acid (PMN P-91-838) is subject to reporting under this section for the significant new...

  9. 40 CFR 721.10140 - Phosphoric acid, tin (2+) salt (2:3).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Phosphoric acid, tin (2+) salt (2:3... Specific Chemical Substances § 721.10140 Phosphoric acid, tin (2+) salt (2:3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as phosphoric acid, tin...

  10. 40 CFR 721.10140 - Phosphoric acid, tin (2+) salt (2:3).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Phosphoric acid, tin (2+) salt (2:3... Specific Chemical Substances § 721.10140 Phosphoric acid, tin (2+) salt (2:3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as phosphoric acid, tin...

  11. 40 CFR 721.10140 - Phosphoric acid, tin (2+) salt (2:3).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Phosphoric acid, tin (2+) salt (2:3... Specific Chemical Substances § 721.10140 Phosphoric acid, tin (2+) salt (2:3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as phosphoric acid, tin...

  12. 40 CFR 721.10140 - Phosphoric acid, tin (2+) salt (2:3).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Phosphoric acid, tin (2+) salt (2:3... Specific Chemical Substances § 721.10140 Phosphoric acid, tin (2+) salt (2:3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as phosphoric acid, tin...

  13. 40 CFR 721.10140 - Phosphoric acid, tin (2+) salt (2:3).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Phosphoric acid, tin (2+) salt (2:3... Specific Chemical Substances § 721.10140 Phosphoric acid, tin (2+) salt (2:3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as phosphoric acid, tin...

  14. 40 CFR 721.7785 - Substituted alkyl aminomethylene polyphosphonic acid, salt (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... polyphosphonic acid, salt (generic). 721.7785 Section 721.7785 Protection of Environment ENVIRONMENTAL PROTECTION... acid, salt (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a substituted alkylamino methylene polyphosphonic acid,...

  15. 40 CFR 721.7785 - Substituted alkyl aminomethylene polyphosphonic acid, salt (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... polyphosphonic acid, salt (generic). 721.7785 Section 721.7785 Protection of Environment ENVIRONMENTAL PROTECTION... acid, salt (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a substituted alkylamino methylene polyphosphonic acid,...

  16. 40 CFR 721.7785 - Substituted alkyl aminomethylene polyphosphonic acid, salt (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... polyphosphonic acid, salt (generic). 721.7785 Section 721.7785 Protection of Environment ENVIRONMENTAL PROTECTION... acid, salt (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a substituted alkylamino methylene polyphosphonic acid,...

  17. 40 CFR 721.10370 - Phosphonic acid, p-octyl-, lanthanum (3+) salt (2:1).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Phosphonic acid, p-octyl-, lanthanum... New Uses for Specific Chemical Substances § 721.10370 Phosphonic acid, p-octyl-, lanthanum (3+) salt... substance identified as phosphinic acid, p-octyl-, lanthanum (3+) salt (2:1) (PMN P-10-99; CAS No....

  18. 40 CFR 721.10370 - Phosphonic acid, p-octyl-, lanthanum (3+) salt (2:1).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Phosphonic acid, p-octyl-, lanthanum... New Uses for Specific Chemical Substances § 721.10370 Phosphonic acid, p-octyl-, lanthanum (3+) salt... substance identified as phosphinic acid, p-octyl-, lanthanum (3+) salt (2:1) (PMN P-10-99; CAS No....

  19. 40 CFR 721.10370 - Phosphonic acid, p-octyl-, lanthanum (3+) salt (2:1).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Phosphonic acid, p-octyl-, lanthanum... New Uses for Specific Chemical Substances § 721.10370 Phosphonic acid, p-octyl-, lanthanum (3+) salt... substance identified as phosphinic acid, p-octyl-, lanthanum (3+) salt (2:1) (PMN P-10-99; CAS No....

  20. 40 CFR 721.3031 - Boric acid (H3BO3), zinc salt (2=3).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Boric acid (H3BO3), zinc salt (2=3... Substances § 721.3031 Boric acid (H3BO3), zinc salt (2=3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as boric acid (H3BO3), zinc salt (2=3) (PMN...

  1. 40 CFR 721.3031 - Boric acid (H3BO3), zinc salt (2=3).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Boric acid (H3BO3), zinc salt (2=3... Substances § 721.3031 Boric acid (H3BO3), zinc salt (2=3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as boric acid (H3BO3), zinc salt (2=3) (PMN...

  2. 40 CFR 721.3031 - Boric acid (H3BO3), zinc salt (2=3).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Boric acid (H3BO3), zinc salt (2=3... Substances § 721.3031 Boric acid (H3BO3), zinc salt (2=3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as boric acid (H3BO3), zinc salt (2=3) (PMN...

  3. 40 CFR 721.3031 - Boric acid (H3BO3), zinc salt (2=3).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Boric acid (H3BO3), zinc salt (2=3... Substances § 721.3031 Boric acid (H3BO3), zinc salt (2=3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as boric acid (H3BO3), zinc salt (2=3) (PMN...

  4. 40 CFR 721.3031 - Boric acid (H3BO3), zinc salt (2=3).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Boric acid (H3BO3), zinc salt (2=3... Substances § 721.3031 Boric acid (H3BO3), zinc salt (2=3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as boric acid (H3BO3), zinc salt (2=3) (PMN...

  5. Salts of phenylacetic acid and 4-hydroxyphenylacetic acid with Cinchona alkaloids: Crystal structures, thermal analysis and FTIR spectroscopy

    NASA Astrophysics Data System (ADS)

    Amombo Noa, Francoise M.; Jacobs, Ayesha

    2016-06-01

    Seven salts were formed with phenylacetic acid (PAA), 4-hydroxyphenylacetic acid (HPAA) and the Cinchona alkaloids; cinchonidine (CIND), quinidine (QUID) and quinine (QUIN). For all the structures the proton was transferred from the carboxylic acid of the PAA/HPAA to the quinuclidine nitrogen of the respective Cinchona alkaloid. For six of the salts, water was included in the crystal structures with one of these also incorporating an isopropanol solvent molecule. However HPAA co-crystallised with quinine to form an anhydrous salt, (HPAA-)(QUIN+). The thermal stability of the salts were determined and differential scanning calorimetry revealed that the (HPAA-)(QUIN+) salt had the highest thermal stability compared to the other salt hydrates. The salts were also characterized using Fourier transform infrared spectroscopy. (PAA-)(QUID+)·H2O and (PAA-)(QUIN+)·H2O are isostructural and Hirshfeld surface analysis was completed to compare the intermolecular interactions in these two structures.

  6. Detailed spectroscopic analysis of chloride salt deposits in Terra Sirenum, Mars

    NASA Astrophysics Data System (ADS)

    Osterloo, M. M.; Glotch, T. D.; Bandfield, J. L.

    2015-12-01

    Chloride salt-bearing deposits have been identified throughout the southern highlands of Mars [1] based on the lack of diagnostic spectral features of anhydrous chlorides in both the visible near infrared (VNIR) and middle infrared (MIR) wavelength ranges [1,2]. A puzzling aspect of martian chloride deposits is the apparent lack of other weathering or evaporite phases associated with most of the deposits. A global analysis over the chloride salt sites conducted by [3] found that only ~9% of the deposits they analyzed were associated with minerals such as phyllosilicates. Most of these occurrences are in Terra Sirenum where [4] noted that salt-bearing deposits lie stratigraphically above Noachian phyllosilicates. Although a variety of formation mechanisms have been proposed for these intriguing deposits, detailed geologic mapping by [5] suggests that surface water and evaporation played a dominant role. On Earth, evaporative settings are often characterized by a multitude of evaporite and phyllosilicate phases including carbonates, sulfates, and nitrates. [6] evaluated chemical divides and brine evolution for martian systems and their results indicate three pathways wherein late-stage brines favor chloride precipitation. In each case the pathway to chloride formation includes precipitation of carbonates (calcite, siderite, and/or magnesite) and sulfates (gypsum, melanterite, and/or epsomite). Here, we present the results of our detailed and systematic spectroscopic study to identify additional evaporite phases associated with salt/silicate mixtures in Terra Sirenum. [1] Osterloo et al. (2008) Science, 319, [2] Glotch, T. D. et al. (2013) Lunar and Planet. Sci. XLIV, abstract #1549 [3] Ruesch, O. et al. (2012), J. Geophys. Res., 117, E00J13 [4] Glotch, T. D. et al. (2010) Geophys. Res. Lett. 37, L16202, [5] Osterloo, M. M. and B. M Hynek (2015) Lunar and Planet. Sci XLVI. Abstract #1054 [6] Tosca, N. J. and S. M. McLennan (2006), Earth and Planet. Sci. Lett., 241.

  7. 40 CFR 721.10097 - Disubstituted benzenesulfonic acid, alkali metal salt (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ..., alkali metal salt (generic). 721.10097 Section 721.10097 Protection of Environment ENVIRONMENTAL... metal salt (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as disubstituted benzenesulfonic acid, alkali metal salt (PMN...

  8. 40 CFR 721.10097 - Disubstituted benzenesulfonic acid, alkali metal salt (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ..., alkali metal salt (generic). 721.10097 Section 721.10097 Protection of Environment ENVIRONMENTAL... metal salt (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as disubstituted benzenesulfonic acid, alkali metal salt (PMN...

  9. 40 CFR 721.10097 - Disubstituted benzenesulfonic acid, alkali metal salt (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ..., alkali metal salt (generic). 721.10097 Section 721.10097 Protection of Environment ENVIRONMENTAL... metal salt (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as disubstituted benzenesulfonic acid, alkali metal salt (PMN...

  10. 40 CFR 721.10097 - Disubstituted benzenesulfonic acid, alkali metal salt (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ..., alkali metal salt (generic). 721.10097 Section 721.10097 Protection of Environment ENVIRONMENTAL... metal salt (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as disubstituted benzenesulfonic acid, alkali metal salt (PMN...

  11. Acid deposition: Atmospheric processes in Eastern North America

    SciTech Connect

    Not Available

    1983-01-01

    This report examines scientific evidence on the relationship between emissions of acid-forming pollutants and damage to sensitive ecosystems from acid rain and other forms of acid deposition. The report's conclusions represent the most authoritative statement yet that reductions in emissions of these pollutants will result in proportional reductions in acid rain.

  12. Salt-Driven Deposition of Thermoresponsive Polymer-Coated Metal Nanoparticles on Solid Substrates.

    PubMed

    Zhang, Zhiyue; Maji, Samarendra; da Fonseca Antunes, André B; De Rycke, Riet; Hoogenboom, Richard; De Geest, Bruno G

    2016-06-13

    Here we report on a simple, generally applicable method for depositing metal nanoparticles on a wide variety of solid surfaces under all aqueous conditions. Noble-metal nanoparticles obtained by citrate reduction followed by coating with thermoresponsive polymers spontaneously form a monolayer-like structure on a wide variety of substrates in presence of sodium chloride whereas this phenomenon does not occur in salt-free medium. Interestingly, this phenomenon occurs below the cloud point temperature of the polymers and we hypothesize that salt ion-induced screening of electrostatic charges on the nanoparticle surface entropically favors hydrophobic association between the polymer-coated nanoparticles and a hydrophobic substrate. PMID:27142455

  13. Nature and Origin of Volcanogenic Salts Deposits around the Crater of Erebus volcano, Antarctica

    NASA Astrophysics Data System (ADS)

    Kammerer, M. M.; Kyle, P. R.; Dunbar, N. W.

    2010-12-01

    Volcanogenic salt deposits (VSD) are widespread around the summit crater of the active 3794-meter high Erebus volcano in Antarctica. The distribution, composition and formation of the salts provide insight into degassing of the phonolite lava lake and the interaction of the gas plume with the snow and rocks around the summit crater. The greatest accumulations of VSD are located within 1 km of the active crater and are found under rocks and in crevices in the lava flows as white to yellow incrustations, massive deposits, efflorescences, and needles. The VSD are most abundant downwind of the crater where individual VSD accumulations of 20g or more are common. The VSD are not associated with fumaroles or fumarolic ice towers but form under the ambient -20 to -60 oC temperatures. The formation of the salts under such extreme temperatures conditions may have application to salt formation at other active planetary volcanoes. Previous XRD analyses of Erebus VSD have positively identified halite, gypsum, alunite, thenardite, sylvite, mirabilite, and calcite, with numerous tentatively identified phases. SEM observations of VSD indicate that the salts are well crystallized on a very fine scale, with crystal size ranging between 1 to 20 microns. One of the most common crystal morphologies consists of well-formed columnar crystals, although blocky, platy and acicular crystals are also observed. Qualitative electron microprobe chemical scans indicate that a wide range of elements are present in the various VSD phases, including Al, Cl, F, Fe, K, Mg, Mn, Na, P, S, and Ti, with multiple salt phases present in each sample. Different crystal morphologies of salt are chemically distinct; the columnar crystals appear to be largely composed of Al, Cl, F, and Fe, platier crystals appear to be composed largely of Na and S, and flat, rectangular crystals are composed of Na and Cl. The Erebus plume, snow, and ice samples around the summit region contain large quantities of Cl, F, and S

  14. Acid deposition and the acidification of soils and waters

    SciTech Connect

    Reuss, J.O.; Johnson, D.W.

    1985-01-01

    A conceptual model of acid deposition is presented consistent with established physicochemical principles and the bulk of available information. The authors seek to provide insight into probable long-term effects of acid deposition; a testable hypotheses; plus design and interpretation of the research. (PSB)

  15. Effects of Buffer Salt Concentration on the Dominated Deposition Mechanism and Optical Characteristics of Chemically Deposited Cadmium Sulfide Thin Films

    NASA Astrophysics Data System (ADS)

    Kakhaki, Z. Makhdoumi; Youzbashi, A.; Sangpour, P.; Kazemzadeh, A.; Naderi, N.; Bazargan, A. M.

    2016-02-01

    Effects of buffer salt concentration on the rate of deposition, dominated deposition mechanism and subsequently the structural, morphological, and optical properties of cadmium sulfide (CdS) thin films deposited by chemical bath deposition (CBD) on glass substrate were investigated. The precursors were chosen to be cadmium chloride (CdCl2) as the cadmium source, thiourea (CS(NH2)2) as the sulfur source, ammonium nitrate (NH4NO3) as the buffer salt and ammonia as the complexing agent and the pH controller. The influence of the NH4NO3 concentration on the structure, morphology, film uniformity, stoichiometry and optical properties of CdS thin films was also studied by X-ray diffractometer (XRD), field emission scanning electron microscope (FE-SEM), energy dispersive X-ray (EDX) spectroscope, uv-visible and photoluminescence (PL) spectroscopes. The XRD studies revealed that all the deposited films exhibited a (002)h/(111)c preferred orientation. The crystallite size was increased from 20nm to 30nm by the increase of concentration of NH4NO3 from 0.5M to 2.5M. The morphology of CdS thin films were agglomerated spherical particles consisted of smaller particles. The surface of thin films deposited at the NH4NO3 concentration of 0.5M was compact and smooth. The increase of the concentration of NH4NO3 decreased the packing density of the films. The optical band gap was in the range of 2.25-2.4eV, which was decreased by the decrement of packing density. The PL spectra showed two peaks centered at 400nm and 500nm which are attributed to violet and band-to-band emissions, respectively.

  16. One-step large-scale deposition of salt-free DNA origami nanostructures

    PubMed Central

    Linko, Veikko; Shen, Boxuan; Tapio, Kosti; Toppari, J. Jussi; Kostiainen, Mauri A.; Tuukkanen, Sampo

    2015-01-01

    DNA origami nanostructures have tremendous potential to serve as versatile platforms in self-assembly -based nanofabrication and in highly parallel nanoscale patterning. However, uniform deposition and reliable anchoring of DNA nanostructures often requires specific conditions, such as pre-treatment of the chosen substrate or a fine-tuned salt concentration for the deposition buffer. In addition, currently available deposition techniques are suitable merely for small scales. In this article, we exploit a spray-coating technique in order to resolve the aforementioned issues in the deposition of different 2D and 3D DNA origami nanostructures. We show that purified DNA origamis can be controllably deposited on silicon and glass substrates by the proposed method. The results are verified using either atomic force microscopy or fluorescence microscopy depending on the shape of the DNA origami. DNA origamis are successfully deposited onto untreated substrates with surface coverage of about 4 objects/mm2. Further, the DNA nanostructures maintain their shape even if the salt residues are removed from the DNA origami fabrication buffer after the folding procedure. We believe that the presented one-step spray-coating method will find use in various fields of material sciences, especially in the development of DNA biochips and in the fabrication of metamaterials and plasmonic devices through DNA metallisation. PMID:26492833

  17. One-step large-scale deposition of salt-free DNA origami nanostructures

    NASA Astrophysics Data System (ADS)

    Linko, Veikko; Shen, Boxuan; Tapio, Kosti; Toppari, J. Jussi; Kostiainen, Mauri A.; Tuukkanen, Sampo

    2015-10-01

    DNA origami nanostructures have tremendous potential to serve as versatile platforms in self-assembly -based nanofabrication and in highly parallel nanoscale patterning. However, uniform deposition and reliable anchoring of DNA nanostructures often requires specific conditions, such as pre-treatment of the chosen substrate or a fine-tuned salt concentration for the deposition buffer. In addition, currently available deposition techniques are suitable merely for small scales. In this article, we exploit a spray-coating technique in order to resolve the aforementioned issues in the deposition of different 2D and 3D DNA origami nanostructures. We show that purified DNA origamis can be controllably deposited on silicon and glass substrates by the proposed method. The results are verified using either atomic force microscopy or fluorescence microscopy depending on the shape of the DNA origami. DNA origamis are successfully deposited onto untreated substrates with surface coverage of about 4 objects/mm2. Further, the DNA nanostructures maintain their shape even if the salt residues are removed from the DNA origami fabrication buffer after the folding procedure. We believe that the presented one-step spray-coating method will find use in various fields of material sciences, especially in the development of DNA biochips and in the fabrication of metamaterials and plasmonic devices through DNA metallisation.

  18. Do the paleolimnological reconstructions reflect the influence of acid deposition?

    SciTech Connect

    Smirnov, D.Y.

    1996-12-31

    The using possibility of paleolimnological analyses was considered with the documentation aim of acid-forming substances distant transfer on territory of Northern Fennoscandia. The Holocene and ancient interglacial lakes pH-and alkalinity trends, reconstructed by means of bottom sediments diatomic analyses, were studied. It has been made evident that the tendency to sharp changes of these data is revealed on final stages of interglacial periods. At that time the high amplitude of climatic changes with low periodicity is resulting in catastrophic changes of landscapes in the frames of water-catchments bodies. During the last millennium the climatic situation in the Northern Fennoscandia was changing repeatedly (Medieval Warm Epoch, Little Ice Age, the rise in temperature in 20-40`s of XXth century). In the Little Ice Age (XVI-XIX centuries) the decrease of average annual temperature and intensification of winds velocity have caused a rapid retreat of latitudinal and high-altitude forest boundaries, accompanied by sharp reconstruction of tundra-,forest-tundra-and northern taiga landscapes. These processes have accelerated due to the enforcement of economic activity which caused the destruction of vegetation cover (salt-working, and ship-building since the XIXth century, pasture of reindeer herds since the end of XIXth century). Acidifying of ground and surface waters in the current century could be caused by the increased entry of organic acids, as a result of plant residues decomposition. The decomposition process was activated in the end of XIXth - beginning of XXth century in connection with the rise of temperature and increase of precipitation. Thus, the trends in pH and alkalinity changes in this region can not be used as indicators of acid-forming substances atmospheric deposition increase.

  19. Catalyst of a metal heteropoly acid salt that is insoluble in a polar solvent on a non-metallic porous support and method of making

    DOEpatents

    Wang, Yong [Richland, WA; Peden, Charles H. F. [West Richland, WA; Choi, Saemin [Richland, WA

    2002-10-29

    The present invention includes a catalyst having (a) a non-metallic support having a plurality of pores; (b) a metal heteropoly acid salt that is insoluble in a polar solvent on the non-metallic support; wherein at least a portion of the metal heteropoly acid salt is dispersed within said plurality of pores. The present invention also includes a method of depositing a metal heteropoly acid salt that is insoluble in a polar solvent onto a non-metallic support having a plurality of pores. The method has the steps of: (a) obtaining a first solution containing a first precursor of a metal salt cation; (b) obtaining a second solution containing a second precursor of a heteropoly acid anion in a solvent having a limited dissolution potential for said first precursor; (c) impregnating the non-metallic support with the first precursor forming a first precursor deposit within the plurality of pores, forming a first precursor impregnated support; (d) heating said first precursor impregnated support forming a bonded first precursor impregnated support; (e) impregnating the second precursor that reacts with the precursor deposit and forms the metal heteropoly acid salt.

  20. Catalyst Of A Metal Heteropoly Acid Salt That Is Insoluble In A Polar Solvent On A Non-Metallic Porous Support And Method Of Making

    DOEpatents

    Wang. Yong; Peden. Charles H. F.; Choi. Saemin

    2004-11-09

    The present invention includes a catalyst having (a) a non-metallic support having a plurality of pores; (b) a metal heteropoly acid salt that is insoluble in a polar solvent on the non-metallic support; wherein at least a portion of the metal heteropoly acid salt is dispersed within said plurality of pores. The present invention also includes a method of depositing a metal heteropoly acid salt that is insoluble in a polar solvent onto a non-metallic support having a plurality of pores. The method has the steps of: (a) obtaining a first solution containing a first precursor of a metal salt cation; (b) obtaining a second solution containing a second precursor of a heteropoly acid anion in a solvent having a limited dissolution potential for said first precursor; (c) impregnating the non-metallic support with the first precursor forming a first precursor deposit within the plurality of pores, forming a first precursor impregnated support; (d) heating said first precursor impregnated support forming a bonded first precursor impregnated support; (e) impregnating the second precursor that reacts with the precursor deposit and forms the metal heteropoly acid salt.

  1. The Tiberias Basin salt deposits and their effects on lake salinity

    NASA Astrophysics Data System (ADS)

    Inbar, Nimrod; Rosenthal, Eliahu; Möller, Peter; Yellin-Dror, Annat; Guttman, Josef; Siebert, Christian; Magri, Fabien

    2015-04-01

    Lake Tiberias is situated in one of the pull-apart basins comprising the Dead Sea transform. The Tiberias basin extends along the northern boundary of the Lower Jordan Rift Valley (LJRV) which is known for its massive salt deposits, mostly at its southern end, at the Dead Sea basin. Nevertheless, prior to the drilling of Zemah-1 wildcat, drilled close to the southern shores of Lake Tiberias, the Tiberias Basin was considered rather shallow and free of salt deposits (Starinsky, 1974). In 1983, Zemah-1 wildcat penetrated 2.8 km thick sequence of sedimentary and magmatic rocks of which 980m are salt deposits (Marcus et al., 1984). Recent studies, including the presented geophysical investigations, lay out the mechanisms of salt deposition in the Tiberias basin and estimate its abundance. Supported by seismic data, our interpreted cross-sections display relatively thick salt deposits distributed over the entire basin. Since early days of hydrological research in the area, saline springs are known to exist at Lake Tiberias' surroundings. Water temperatures in some of the springs indicate their origin to be at depths of 2-3 km (Simon and Mero, 1992). In the last decade, several studies suggested that the salinity of springs may be attributed, at least partially, to the Zemah-1 salt deposits. Chemical justification was attributed to post-halite minerals which were thought to be present among those deposits. This hypothesis was never verified. Moreover, Möller et al. (2011) presented a calculation contradicting this theory. In addition to the geophysical investigations, numerical models of thermally driven flow, examine the possible fluid dynamics developing near salt deposits below the lake and their interactions with springs along the lakeshore (Magri et al., 2015). It is shown that leached halite is too heavy to reach the surface. However, salt diffusing from shallow salt crest may locally reach the western side of the lakeshore. References Magri, F., N. Inbar

  2. ANNULUS CLOSURE TECHNOLOGY DEVELOPMENT INSPECTION/SALT DEPOSIT CLEANING MAGNETIC WALL CRAWLER

    SciTech Connect

    Minichan, R; Russell Eibling, R; James Elder, J; Kevin Kane, K; Daniel Krementz, D; Rodney Vandekamp, R; Nicholas Vrettos, N

    2008-06-01

    The Liquid Waste Technology Development organization is investigating technologies to support closure of radioactive waste tanks at the Savannah River Site (SRS). Tank closure includes removal of the wastes that have propagated to the tank annulus. Although amounts and types of residual waste materials in the annuli of SRS tanks vary, simple salt deposits are predominant on tanks with known leak sites. This task focused on developing and demonstrating a technology to inspect and spot clean salt deposits from the outer primary tank wall located in the annulus of an SRS Type I tank. The Robotics, Remote and Specialty Equipment (RRSE) and Materials Science and Technology (MS&T) Sections of the Savannah River National Laboratory (SRNL) collaborated to modify and equip a Force Institute magnetic wall crawler with the tools necessary to demonstrate the inspection and spot cleaning in a mock-up of a Type I tank annulus. A remote control camera arm and cleaning head were developed, fabricated and mounted on the crawler. The crawler was then tested and demonstrated on a salt simulant also developed in this task. The demonstration showed that the camera is capable of being deployed in all specified locations and provided the views needed for the planned inspection. It also showed that the salt simulant readily dissolves with water. The crawler features two different techniques for delivering water to dissolve the salt deposits. Both water spay nozzles were able to dissolve the simulated salt, one is more controllable and the other delivers a larger water volume. The cleaning head also includes a rotary brush to mechanically remove the simulated salt nodules in the event insoluble material is encountered. The rotary brush proved to be effective in removing the salt nodules, although some fine tuning may be required to achieve the best results. This report describes the design process for developing technology to add features to a commercial wall crawler and the results of the

  3. Viable halobacteria from Permo-Triassic salt deposits and the possibility of extraterrestrial microbial life

    NASA Astrophysics Data System (ADS)

    Stan-Lotter, H.; Radax, C.; Gruber, C.; Legat, A.; Pfaffenhuemer, M.; Wieland, H.

    2001-08-01

    The range of physico-chemical parameters for the presence of life is ever expanding, making it conceivable to search in seemingly inhospitable environments for extraterrestrial forms of life. Extremely halophilic archaebacteria (haloarchaea) were isolated from ancient salt deposits, adding another dimension - potentially exorbitant longevity - to the unusual characteristics of prokaryotic life. Distribution of haloarchaea in salt sediments appears to be world-wide; one particular strain, Halococcus salifodinae, was found in Alpine and Zechstein sediments. By using amplification of 16S rRNA genes with DNA extracted from rock salt, we obtained evidence for numerous haloarchaea, which have not been cultivated yet. Phylogenetic analysis revealed novel taxa within known lineages of haloarchaea. The results could be of relevance for astrobiology: together with the recent findings of halite, sylvite and water in some meteorites, it is intriguing to consider a specific search for extreme halophiles in Mars return samples or other materials from celestial bodies.

  4. ROCKY MOUNTAIN ACID DEPOSITION MODEL ASSESSMENT: EVALUATION OF MESOSCALE ACID DEPOSITION MODELS FOR USE IN COMPLEX TERRAIN

    EPA Science Inventory

    The report includes an evaluation of candidate meteorological models and acid deposition models. The hybrid acid deposition/air quality modeling system for the Rocky Mountains makes use of a mesoscale meteorological model, which includes a new diagnostic wind model, as a driver f...

  5. Effects of acid, salt and soaking time on the dielectric properties of acidified vegetables

    Technology Transfer Automated Retrieval System (TEKTRAN)

    In order to design a continuous microwave process for pasteurization of acidified vegetables, equilibration phenomena in acid and salt solutions must be examined with regards to changes in dielectric properties. The objective of this study was to examine the effects of acid and salt concentration o...

  6. Starch-lipid complexes: Interesting material and applications from amylose-fatty acid salt inclusion complexes

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Aqueous slurries of high amylose starch can be steam jet cooked and blended with aqueous solutions of fatty acid salts to generate materials that contain inclusion complexes between amylose and the fatty acid salt. These complexes are simply prepared on large scale using commercially available steam...

  7. 40 CFR 721.10177 - Phosphoric acid, yttrium(3+) salt (1:1).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Phosphoric acid, yttrium(3+) salt (1:1... Specific Chemical Substances § 721.10177 Phosphoric acid, yttrium(3+) salt (1:1). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as...

  8. 40 CFR 721.10177 - Phosphoric acid, yttrium(3+) salt (1:1).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Phosphoric acid, yttrium(3+) salt (1:1... Specific Chemical Substances § 721.10177 Phosphoric acid, yttrium(3+) salt (1:1). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as...

  9. 40 CFR 721.10177 - Phosphoric acid, yttrium(3+) salt (1:1).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Phosphoric acid, yttrium(3+) salt (1:1... Specific Chemical Substances § 721.10177 Phosphoric acid, yttrium(3+) salt (1:1). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as...

  10. 40 CFR 721.10177 - Phosphoric acid, yttrium(3+) salt (1:1).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Phosphoric acid, yttrium(3+) salt (1:1... Specific Chemical Substances § 721.10177 Phosphoric acid, yttrium(3+) salt (1:1). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as...

  11. 40 CFR 721.10177 - Phosphoric acid, yttrium(3+) salt (1:1).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Phosphoric acid, yttrium(3+) salt (1:1... Specific Chemical Substances § 721.10177 Phosphoric acid, yttrium(3+) salt (1:1). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as...

  12. 78 FR 34648 - Citric Acid and Certain Citrate Salts: Preliminary Results of Countervailing Duty Administrative...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-06-10

    ... Countervailing Duty Order, 74 FR 25705 (May 29, 2009), remains dispositive. A full description of the scope of... International Trade Administration Citric Acid and Certain Citrate Salts: Preliminary Results of Countervailing... review of the countervailing duty (CVD) order on citric acid and citrate salts from the People's...

  13. Bile acid salt binding with colesevelam HCl is not affected by suspension in common beverages.

    PubMed

    Hanus, Martin; Zhorov, Eugene

    2006-12-01

    It has been previously reported that anions in common beverages may bind to bile acid sequestrants (BAS), reducing their capacity for binding bile acid salts. This study examined the ability of the novel BAS colesevelam hydrochloride (HCl), in vitro, to bind bile acid sodium salts following suspension in common beverages. Equilibrium binding was evaluated under conditions of constant time and varying concentrations of bile acid salts in simulated intestinal fluid (SIF). A stock solution of sodium salts of glycochenodeoxycholic acid (GCDC), taurodeoxycholic acid (TDC), and glycocholic acid (GC), was added to each prepared sample of colesevelam HCl. Bile acid salt binding was calculated by high-performance liquid chromatography (HPLC) analysis. Kinetics experiments were conducted using constant initial bile acid salt concentrations and varying binding times. The affinity, capacity, and kinetics of colesevelam HCl binding for GCDC, TDC, and GC were not significantly altered after suspension in water, carbonated water, Coca-Cola, Sprite, grape juice, orange juice, tomato juice, or Gatorade. The amount of bile acid sodium salt bound as a function of time was unchanged by pretreatment with any beverage tested. The in vitro binding characteristics of colesevelam HCl are unchanged by suspension in common beverages. PMID:16937334

  14. Sedimentary characteristics and depositional model of a Paleocene-Eocene salt lake in the Jiangling Depression, China

    NASA Astrophysics Data System (ADS)

    Yu, Xiaocan; Wang, Chunlian; Liu, Chenglin; Zhang, Zhaochong; Xu, Haiming; Huang, Hua; Xie, Tengxiao; Li, Haonan; Liu, Jinlei

    2015-11-01

    We studied the sedimentary characteristics of a Paleocene-Eocene salt lake in the Jiangling Depression through field core observation, thin section identification, scanning electron microscopy, and X-ray diffraction analysis. On the basis of sedimentary characteristics we have summarized the petrological and mineralogical characteristics of the salt lake and proposed 9 types of grade IV salt rhythms. The deposition shows a desalting to salting order of halite-argillaceous-mudstone-mud dolostonemud anhydrock-glauberite-halite. The relationship among grade IV rhythms, water salinity and climate fluctuations was analyzed. Based on the analysis of the relationship between boron content and mudstone color and by combining the mineralogy and sedimentary environment characteristics, we propose that the early and late Paleocene Shashi Formation in the Jiangling Depression was a paleolacustrine depositional environment with a high salt content, which is a representation of the shallow water salt lake depositional model. The middle Paleocene Shashi Formation and the early Eocene Xingouzui Formation were salt and brackish sedimentary environments with low salt content in a deep paleolake, which represents a deep salt lake depositional model.

  15. Plasma-induced surface modification of polydimethylsiloxane aimed at reducing salt and protein deposition.

    PubMed

    De Smet, Nele; Rymarczyk-Machal, Monika; Schacht, Etienne

    2011-01-01

    Polydimethylsiloxane (PDMS) is an elastomer that is widely used in construction and for biological and biomedical applications. The biocompatibility of PDMS was improved by different surface treatment methods, i.e., plasma treatment or a combination of plasma treatment with UV-irradiation or redox initiator, to minimize the effects of deposition of salts and proteins. In this work we used the vinyl monomers sulfobetaine and AMPS which have good biocompatible properties. PMID:21176391

  16. Does livestock grazing affect sediment deposition and accretion rates in salt marshes?

    NASA Astrophysics Data System (ADS)

    Nolte, Stefanie; Müller, Frauke; Schuerch, Mark; Wanner, Antonia; Esselink, Peter; Bakker, Jan P.; Jensen, Kai

    2013-12-01

    Accretion rates, defined as the vertical growth of salt marshes measured in mm per year, may be influenced by grazing livestock in two ways: directly, by increasing soil compaction through trampling, and indirectly, by reducing aboveground biomass and thus decreasing sediment deposition rates measured in g/m² per year. Although accretion rates and the resulting surface elevation change largely determine the resilience of salt marshes to sea-level rise (SLR), the effect of livestock grazing on accretion rates has been little studied. Therefore, this study aimed to investigate the effect of livestock grazing on salt-marsh accretion rates. We hypothesise that accretion will be lower in grazed compared to ungrazed salt marshes. In four study sites along the mainland coast of the Wadden Sea (in the south-eastern North Sea), accretion rates, sediment deposition rates, and soil compaction of grazed and ungrazed marshes were analysed using the 137Cs radionuclide dating method. Accretion rates were on average 11.6 mm yr-1 during recent decades and thus higher than current and projected rates of SLR. Neither accretion nor sediment deposition rates were significantly different between grazing treatments. Meanwhile, soil compaction was clearly affected by grazing with significantly higher dry bulk density on grazed compared to ungrazed parts. Based on these results, we conclude that other factors influence whether grazing has an effect on accretion and sediment deposition rates and that the effect of grazing on marsh growth does not follow a direct causal chain. It may have a great importance when interacting with other biotic and abiotic processes on the marsh.

  17. Stress corrosion cracking of austenitic weld deposits in a salt spray environment

    NASA Astrophysics Data System (ADS)

    Cai, J. B.; Yu, C.; Shiue, R. K.; Tsay, L. W.

    2015-10-01

    ER 308L and 309LMo were utilized as the filler metals for the groove and overlay welds of a 304L stainless steel substrate, which was prepared via a gas tungsten arc-welding process in multiple passes. U-bend and weight-loss tests were conducted by testing the welds in a salt spray containing 10 wt% NaCl at 120 °C. The dissolution of the skeletal structure in the fusion zone (FZ) caused the stress corrosion cracking (SCC) of the weld. The FZ in the cold-rolled condition showed the longest single crack length in the U-bend tests. Moreover, sensitization treatment at 650 °C for 10 h promoted the formation of numerous fine cracks, which resulted in a high SCC susceptibility. The weight loss of the deposits was consistent with the SCC susceptibility of the welds in a salt spray. The 309LMo deposit was superior to the 308L deposit in the salt spray.

  18. Stress corrosion cracking of austenitic weld deposits in a salt spray environment

    NASA Astrophysics Data System (ADS)

    Cai, J. B.; Yu, C.; Shiue, R. K.; Tsay, L. W.

    2015-10-01

    ER 308L and 309LMo were utilized as the filler metals for the groove and overlay welds of a 304L stainless steel substrate, which was prepared via a gas tungsten arc-welding process in multiple passes. U-bend and weight-loss tests were conducted by testing the welds in a salt spray containing 10 wt% NaCl at 120 °C. The dissolution of the skeletal structure in the fusion zone (FZ) caused the stress corrosion cracking (SCC) of the weld. The FZ in the cold-rolled condition showed the longest single crack length in the U-bend tests. Moreover, sensitization treatment at 650 °C for 10 h promoted the formation of numerous fine cracks, which resulted in a high SCC susceptibility. The weight loss of the deposits was consistent with the SCC susceptibility of the welds in a salt spray. The 309LMo deposit was superior to the 308L deposit in the salt spray.

  19. Effect of transition metal salts on the initiated chemical vapor deposition of polymer thin films

    SciTech Connect

    Kwong, Philip; Seidel, Scott; Gupta, Malancha

    2015-05-15

    In this work, the effect of transition metal salts on the initiated chemical vapor deposition of polymer thin films was studied using x-ray photoelectron spectroscopy. The polymerizations of 4-vinyl pyridine and 1H,1H,2H,2H-perfluorodecyl acrylate were studied using copper(II) chloride (CuCl{sub 2}) and iron(III) chloride (FeCl{sub 3}) as the transition metal salts. It was found that the surface coverages of both poly(4-vinyl pyridine) (P4VP) and poly(1H,1H,2H,2H-perfluorodecyl acrylate) were decreased on CuCl{sub 2}, while the surface coverage of only P4VP was decreased on FeCl{sub 3}. The decreased polymer surface coverage was found to be due to quenching of the propagating radicals by the salt, which led to a reduction of the oxidation state of the metal. The identification of this reaction mechanism allowed for tuning of the effectiveness of the salts to decrease the polymer surface coverage through the adjustment of processing parameters such as the filament temperature. Additionally, it was demonstrated that the ability of transition metal salts to decrease the polymer surface coverage could be extended to the fabrication of patterned cross-linked coatings, which is important for many practical applications such as sensors and microelectronics.

  20. Haloferax chudinovii sp. nov., a halophilic archaeon from Permian potassium salt deposits.

    PubMed

    Saralov, Alexander I; Baslerov, Roman V; Kuznetsov, Boris B

    2013-05-01

    Three pigmented strains of halophilic archaea (RS75, RS77, RS79) were isolated from the monoliths of mottled sylvinite from the Verkhnekamsk salt deposit (Solikamsk, Russia). The cells were nonmotile, gram-negative, pleomorphic, disk-shaped or ovoid, 0.8-1.0 × 1.5-2.5 μm. The organism was a chemoorganotrophic obligate aerobe producing catalase and oxidase. A number of carbohydrates and carboxylic acids were used as growth substrates. Growth occurred in the presence of 7-27% NaCl (with the optimum at 15-18%), 0.02-20% KCl (0.2-1%), 0.2-16% MgCl2 (2-3%), in the temperature range from 23 to 51 °C (40-45 °C), and pH 5.5-8.0 (6.8-7.0). The membranes contained carotenoids of the bacterioruberin series. Phosphatidylglyceromethylphosphate (PGP-Me), phosphatidylglycerol (PG), sulfated diglycosyl diether (S-DGD-1) predominated among the polar lipids. The DNA G + C content was 64.0-65.0 mol %. Phylogenetic analysis of the 16S rRNA gene sequences showed high similarity of the new strains to Haloferax species: H. denitrificans (99.2%) and H. volcanii (99.1%), H. larsenii (96.9%) and H. elongans (96.6%). DNA-DNA hybridization revealed 93-95% similarity between strain RS75 and strains RS77 and RS79; the similarity levels between strain RS75 and the type strains of Haloferax denitrificans VKM B-1754(T) and Halobacterium salinarum VKM B-1769(T) were 50 and 10%, respectively. According to its phenotypic and genotypic characteristics, the organism was classified as a member of the genus Haloferax, forming a new species with the proposed name Haloferax chudinovii sp. nov. type strain is RS75(T) (=VKPM B-11279(T)). PMID:23525908

  1. Suspended sediment deposition and trapping efficiency in a Delaware salt marsh

    NASA Astrophysics Data System (ADS)

    Moskalski, Susanne M.; Sommerfield, Christopher K.

    2012-02-01

    This study examined sediment deposition and retention in a section of salt marsh in the St. Jones River estuary in Delaware. Sediment traps, siphon samplers, a LISST particle sizer, and four water level sensors were deployed in a 100 m by 200 m grid over the course of a spring tide in June 2007. The objective was to determine the relative influences of suspended sediment concentration, settling velocity, tidal hydroperiod, and vegetation density on sediment deposition and trapping efficiency within a small section of marsh. Hydroperiod is not a major contributor to sediment deposition in the study plot. Spatial patterns in depositional processes on tidal timescales are instead primarily controlled by overmarsh SSC, settling velocity, and distance from the tidal channel. Trapping efficiency, or the ratio of measured deposition and the amount of sediment available for deposition, decreased with distance away from the tidal channel, indicating that less of the available suspended sediment was deposited in the marsh interior. The suspended particles were flocculated, but floc sizes decreased with distance away from the tidal channel.

  2. ROCKY MOUNTAIN ACID DEPOSITION MODEL ASSESSMENT: ACID RAIN MOUNTAIN MESOSCALE MODEL (ARM3)

    EPA Science Inventory

    The Acid Rain Mountain Mesoscale Model (ARM3) is a mesoscale acid deposition/air quality model that was developed for calculating incremental acid deposition (sulfur and nitrogen species) and pollutant concentration impacts in complex terrain. The model was set up for operation w...

  3. Acidity and mineral composition of precipitation in Moscow: Influence of deicing salts

    NASA Astrophysics Data System (ADS)

    Eremina, I. D.; Aloyan, A. E.; Arutyunyan, V. O.; Larin, I. K.; Chubarova, N. E.; Yermakov, A. N.

    2015-11-01

    Monitoring data and analysis of the variation in acidity and mineral composition of atmospheric precipitation in Moscow in 2012 are presented. We have found that the chloride anions in the precipitation are largely caused by chlorides of deicing salts. Here, the chloride anions, along with metal chlorides (components of deicing salts), are partly caused by dissolved hydrogen chloride. The appearance of hydrogen chloride in the atmosphere of Moscow has been shown to result from heterophase chemical reactions involving deicing salts. We have obtained preliminary estimates for the scales of the effect of these salts on the mineral composition and acidity of precipitations in Moscow.

  4. 40 CFR 721.10135 - Phosphinic acid, P,P-diethyl-, zinc salt (2:1).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Phosphinic acid, P,P-diethyl-, zinc... Specific Chemical Substances § 721.10135 Phosphinic acid, P,P-diethyl-, zinc salt (2:1). (a) Chemical... acid, P,P-diethyl-, zinc salt (2:1) (PMN P-05-11; CAS No. 284685-45-6) is subject to reporting...

  5. 40 CFR 721.10135 - Phosphinic acid, P,P-diethyl-, zinc salt (2:1).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Phosphinic acid, P,P-diethyl-, zinc... Specific Chemical Substances § 721.10135 Phosphinic acid, P,P-diethyl-, zinc salt (2:1). (a) Chemical... acid, P,P-diethyl-, zinc salt (2:1) (PMN P-05-11; CAS No. 284685-45-6) is subject to reporting...

  6. 40 CFR 721.10135 - Phosphinic acid, P,P-diethyl-, zinc salt (2:1).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Phosphinic acid, P,P-diethyl-, zinc... Specific Chemical Substances § 721.10135 Phosphinic acid, P,P-diethyl-, zinc salt (2:1). (a) Chemical... acid, P,P-diethyl-, zinc salt (2:1) (PMN P-05-11; CAS No. 284685-45-6) is subject to reporting...

  7. 40 CFR 721.10135 - Phosphinic acid, P,P-diethyl-, zinc salt (2:1).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Phosphinic acid, P,P-diethyl-, zinc... Specific Chemical Substances § 721.10135 Phosphinic acid, P,P-diethyl-, zinc salt (2:1). (a) Chemical... acid, P,P-diethyl-, zinc salt (2:1) (PMN P-05-11; CAS No. 284685-45-6) is subject to reporting...

  8. 40 CFR 721.10135 - Phosphinic acid, P,P-diethyl-, zinc salt (2:1).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Phosphinic acid, P,P-diethyl-, zinc... Specific Chemical Substances § 721.10135 Phosphinic acid, P,P-diethyl-, zinc salt (2:1). (a) Chemical... acid, P,P-diethyl-, zinc salt (2:1) (PMN P-05-11; CAS No. 284685-45-6) is subject to reporting...

  9. 40 CFR 180.1068 - C12-C18 fatty acid potassium salts; exemption from the requirement of a tolerance.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 25 2013-07-01 2013-07-01 false C12-C18 fatty acid potassium salts... RESIDUES IN FOOD Exemptions From Tolerances § 180.1068 C12-C18 fatty acid potassium salts; exemption from the requirement of a tolerance. C12-C18 fatty acids (saturated and unsaturated) potassium salts...

  10. 40 CFR 180.1068 - C12-C18 fatty acid potassium salts; exemption from the requirement of a tolerance.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 24 2014-07-01 2014-07-01 false C12-C18 fatty acid potassium salts... RESIDUES IN FOOD Exemptions From Tolerances § 180.1068 C12-C18 fatty acid potassium salts; exemption from the requirement of a tolerance. C12-C18 fatty acids (saturated and unsaturated) potassium salts...

  11. 40 CFR 180.1068 - C12-C18 fatty acid potassium salts; exemption from the requirement of a tolerance.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 23 2010-07-01 2010-07-01 false C12-C18 fatty acid potassium salts... RESIDUES IN FOOD Exemptions From Tolerances § 180.1068 C12-C18 fatty acid potassium salts; exemption from the requirement of a tolerance. C12-C18 fatty acids (saturated and unsaturated) potassium salts...

  12. 40 CFR 180.1068 - C12-C18 fatty acid potassium salts; exemption from the requirement of a tolerance.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 25 2012-07-01 2012-07-01 false C12-C18 fatty acid potassium salts... RESIDUES IN FOOD Exemptions From Tolerances § 180.1068 C12-C18 fatty acid potassium salts; exemption from the requirement of a tolerance. C12-C18 fatty acids (saturated and unsaturated) potassium salts...

  13. 40 CFR 180.1068 - C12-C18 fatty acid potassium salts; exemption from the requirement of a tolerance.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 24 2011-07-01 2011-07-01 false C12-C18 fatty acid potassium salts... RESIDUES IN FOOD Exemptions From Tolerances § 180.1068 C12-C18 fatty acid potassium salts; exemption from the requirement of a tolerance. C12-C18 fatty acids (saturated and unsaturated) potassium salts...

  14. 21 CFR 872.3490 - Carboxymethylcellulose sodium and/or polyvinylmethylether maleic acid calcium-sodium double salt...

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... polyvinylmethylether maleic acid calcium-sodium double salt denture adhesive. 872.3490 Section 872.3490 Food and Drugs... maleic acid calcium-sodium double salt denture adhesive. (a) Identification. A carboxymethylcellulose sodium and/or polyvinylmethylether maleic acid calcium-sodium double salt denture adhesive is a...

  15. 21 CFR 872.3490 - Carboxymethylcellulose sodium and/or polyvinylmethylether maleic acid calcium-sodium double salt...

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... polyvinylmethylether maleic acid calcium-sodium double salt denture adhesive. 872.3490 Section 872.3490 Food and Drugs... maleic acid calcium-sodium double salt denture adhesive. (a) Identification. A carboxymethylcellulose sodium and/or polyvinylmethylether maleic acid calcium-sodium double salt denture adhesive is a...

  16. 21 CFR 872.3490 - Carboxymethylcellulose sodium and/or polyvinylmethylether maleic acid calcium-sodium double salt...

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... polyvinylmethylether maleic acid calcium-sodium double salt denture adhesive. 872.3490 Section 872.3490 Food and Drugs... maleic acid calcium-sodium double salt denture adhesive. (a) Identification. A carboxymethylcellulose sodium and/or polyvinylmethylether maleic acid calcium-sodium double salt denture adhesive is a...

  17. 21 CFR 872.3490 - Carboxymethylcellulose sodium and/or polyvinylmethylether maleic acid calcium-sodium double salt...

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... polyvinylmethylether maleic acid calcium-sodium double salt denture adhesive. 872.3490 Section 872.3490 Food and Drugs... maleic acid calcium-sodium double salt denture adhesive. (a) Identification. A carboxymethylcellulose sodium and/or polyvinylmethylether maleic acid calcium-sodium double salt denture adhesive is a...

  18. Characterizing putative chloride salt deposits on Mars using THEMIS and TES data

    NASA Astrophysics Data System (ADS)

    Jensen, H. B.; Glotch, T. D.

    2009-12-01

    Previous studies (Osterloo et al., 2008) have located and characterized spectrally unique units on the surface of Mars based on their spectral signatures in mid-IR data collected by the Thermal Emission Imaging System (THEMIS) instrument aboard the 2001 Mars Odyssey spacecraft. The unique spectral slopes associated with these deposits in THEMIS data can be best explained by the admixture of spectrally neutral chloride salts and basaltic materials. These deposits can be recognized in THEMIS daytime infrared images by a distinct aqua-blue color in 9/6/4 (RGB) decorrelation stretch images and a relatively featureless emissivity spectrum that slopes toward lower wavenumbers. Identification of these units has been constrained to the ancient cratered southern highlands of Mars suggesting that water was persistent and widespread, either on the surface or in the near subsurface of Mars early in its history. The objective of this study is to determine the geologic context of these deposits over the Martian landscape as well as to define any spectral variation between defined units, if any. On Earth, chloride salt deposits have three possible origins: (1) precipitation from evaporating surface water (e.g. saline lakes), (2) volcanic outgassing, or (3) direct crystallization (forming crusts). Using MOLA elevation data, the local topography around these spectrally distinct units can be derived and compared. In localities where CRISM FRT data overlaps the deposit positions, the detection of clays indicate a persistent aqueous environment, while their absence may indicate a short lived presence of liquid water at the locality. Variations of spectral slope as well as other spectral characteristics derived from atmospherically corrected daytime THEMIS IR data may indicate variations in the thickness, concentration, and geologic context of the deposits. Through a greater understanding of the geologic environment around these units, we can glean a greater understanding of the

  19. Synthesis, single crystal structure and energy optimization of a multicomponent salt of imidazole and tetrabromoterepthalic acid

    SciTech Connect

    Singha, S.; Kumar, S.; Dey, S. K.

    2015-06-24

    Single crystal of a multicomponent salt (IMTBTP) of imidazole with tetrabromoterepthalic acid has been synthesized by slow evaporation method at room temperature. The crystal structure of the salt has been determined by single crystal x-ray diffraction technique. The supramolecular structure analysis reveals that the multicomponent salt is formed by noncovalent hydrogen bonding interaction and Br···π interaction. The energy optimization and HOMO-LUMO energy gap calculation have been carried out by Density Functional Theory.

  20. The impact of salt tectonics on supra-salt (Lago Mare?) deposits and on the structural evolution of the Cyprus-Eratosthenes collision zone

    NASA Astrophysics Data System (ADS)

    Reiche, Sönke; Hübscher, Christian; Ehrhardt, Axel

    2015-04-01

    Averagely 1.5 km thick Messinian evaporites laterally continue from the Levant Basin, easternmost Mediterranean Sea, into the collision zone between Cyprus and Eratosthenes Seamount where incipient continent-continent-collision is believed to occur. In this study, the impact of Messinian evaporites on the structural evolution of the collision zone is investigated for the first time based on a comprehensive set of seismic reflection profiles. Results show that the collision zone may be subdivided into an eastern and a western domain. In the eastern part, bordered by Eratosthenes Seamount and the Hecataeus Rise, compressionally thickened autochthonous salt is observed. Sub- and supra-salt deposits within this area appear to be in the stage of active accretion. Further west, between Cyprus and Eratosthenes Seamount strongly deformed allochthonous salt has evidently started to advance across sediments of post-Messinian age. In this domain, previously active sediment accretion at the Cyprus margin has now become inactive and shortening is largely accommodated at the leading edge of the allochthonous salt sheet. Such observations bear important implications for the structural interrelation between salt tectonics and the evolution of a young collision zone. On top of highly deformed mobile Messinian evaporites, up to 700 m thick late Messinian supra-salt deposits are mapped within the western part of the Cyprus - Eratosthenes collision zone. Their uppermost 200 m were drilled in the course of ODP Leg 160 (Site 968) and interpreted as Lago Mare sediments, deposited during the final stage of the Messinian Salinity Crisis (Robertson, 1998). These sediments occupy small sub-basins flanked by salt diapirs, indicating a salt-tectonic control on late Messinian sediment deposition. Distribution of these sediments may have further been controlled by sea-level, inferred from rapid eastward thinning and pinchout of Messinian supra-salt deposits towards the Levant Basin

  1. ESTIMATES OF CLOUD WATER DEPOSITION AT MOUNTAIN DEPOSITION AT MOUNTAIN ACID DEPOSITION PROGRAM SITES IN THE APPALACHIAN MOUNTAINS

    EPA Science Inventory

    Cloud water deposition was estimated at three high elevation sites in the Appalachian Mountains of the eastern United States (Whiteface Mountain, NY, Whitetop Mountain, VA, and Clingrnan's Dome, TN) from 1994 through 1999 as part of the Mountain Acid Deposition Program (MADPro). ...

  2. On the isolation of halophilic microorganisms from salt deposits of great geological age

    NASA Technical Reports Server (NTRS)

    Stan-Lotter, Helga; Denner, Ewald

    1993-01-01

    From salt sediments of Triassic or Permian age from various locations in the world halophilic microorganisms were isolated. Molecular characteristics of several of the isolates suggested they belong to the archaebacteria. One group appears to represent novel strains; several properties of one such isolate, strain BIp, are described here. The existence of viable microorganisms in ancient sediment would have great implications with respect to our notions on evolution, the research for life in extraterrestrial environments, and the longterm survival of functional biological structures. Of crucial importance is thus the question if these microorganisms existed in the salt since the time of deposition or invaded at some later date. Some suggestions to address these issues experimentally are discussed.

  3. On the Isolation of Halophilic Microorganisms from Salt Deposits of Great Geological Age

    NASA Technical Reports Server (NTRS)

    Stan-Lotter, Helga; Denner, Ewald; Orans, Robin (Editor)

    1993-01-01

    From salt sediments of Triassic or Permian ace from various locations in the world halophilic microorganisms were isolated. Molecular characteristics of several of the isolates suggested they belong to the archaebacteriae. One group appears to represent novel strains; several properties or one such isolate, strain BIp, are described here. The existence of viable microorganisms in ancient sediments would have great implications with respect to our notions on evolution, the search for life in extraterrestrial environments and the long- term survival of functional biological structures. Of crucial importance is thus the question if these microorganisms existed in the salt since the time of deposition or invaded at some later date. Some suggestions to address these issues experimentally are discussed.

  4. Halite depositional facies in a solar salt pond: A key to interpreting physical energy and water depth in ancient deposits

    SciTech Connect

    Handford, C.R. )

    1990-08-01

    Subaqueous deposits of aragonite, gypsum, and halite are accumulating in shallow solar salt ponds constructed in the Pekelmeer, a sea-level salina on Bonaire, Netherlands Antilles. Several halite facies are deposited in the crystallizer ponds in response to difference in water depth and wave energy. Cumulate halite, which originates as floating rafts, is present only along the protected, upwind margins of ponds where low-energy conditions foster their formation and preservation. Cornet crystals with peculiar mushroom- and mortarboard-shaped caps precipitate in centimetre-deep brine sheets within a couple of metres of the upwind or low-energy margins. Downwind from these margins, cornet and chevron halite precipitate on the pond floors in water depths ranging from a few centimetres to {approximately} 60 cm. Halite pisoids with radial-concentric structure are precipitated in the swash zone along downwind high-energy shorelines where they form pebbly beaches. This study suggests that primary halite facies are energy and/or depth dependent and that some primary features, if preserved in ancient halite deposits, can be used to infer physical energy conditions, subenvironments such as low- to high-energy shorelines, and extremely shallow water depths in ancient evaporite basins.

  5. Factors affecting response of surface waters to acidic deposition

    SciTech Connect

    Turner, R.S.; Johnson, D.W.; Elwood, J.W.; Van Winkle, W.; Clapp, R.B.; Reuss, J.O.

    1986-04-01

    Knowledge of watershed hydrology and of the biogeochemical reactions and elemental pools and fluxes occurring in watersheds can be used to classify the response of watersheds and surface waters to acidic deposition. A conceptual mosel is presented for classifying watersheds into those for which (1) surface water chemistry will change rapidly with deposition quality (direct response) (2) surface water chemistry will change only slowly over time (delayed response), and (3) surface water chemistry will not change significantly, even with continued acidic deposition (capacity-protected). Techniques and data available for classification of all watersheds in a region into these categories are discussed.

  6. Structure of seven organic salts assembled from 2,6-diaminopyridine with monocarboxylic acids, dicarboxylic acids, and tetracarboxylic acids

    NASA Astrophysics Data System (ADS)

    Gao, Xingjun; Zhang, Huan; Wen, Xianhong; Liu, Bin; Jin, Shouwen; Wang, Daqi

    2015-08-01

    Studies concentrating on non-covalent interactions between the organic base of 2,6-diaminopyridine, and carboxylic acids have led to an increased understanding of the role 2,6-diaminopyridine in binding with carboxylic acid derivatives. Here anhydrous and hydrated multi-component organic acid-base salts of 2,6-diaminopyridine have been prepared with the carboxylic acids as nicotinic acid, o-chlorobenzoic acid, 1,3-benzodioxole-5-carboxylic acid, 3,5-dinitrosalicylic acid, 4-nitro-phthalic acid, 1,4-cyclohexanedicarboxylic acid, and butane-1,2,3,4-tetracarboxylic acid. The seven crystalline compounds were characterized by X-ray diffraction analysis, infrared (IR), melting point (mp), and elemental analysis. All structures adopted the hetero R22(8) supramolecular synthons. The supramolecular architectures bear extensive Nsbnd H⋯N, Osbnd H⋯N, Osbnd H⋯O, Nsbnd H⋯O, and CH⋯O associations as well as other nonbonding contacts as CHsbnd N, CH2sbnd O, π-π, C-π, O-π, Cl-π, Clsbnd O, and Osbnd O interactions. The role of weak and strong hydrogen bonding in the crystal packing is ascertained.

  7. Comparison of peak shape in hydrophilic interaction chromatography using acidic salt buffers and simple acid solutions.

    PubMed

    Heaton, James C; Russell, Joseph J; Underwood, Tim; Boughtflower, Robert; McCalley, David V

    2014-06-20

    The retention and peak shape of neutral, basic and acidic solutes was studied on hydrophilic interaction chromatography (HILIC) stationary phases that showed both strong and weak ionic retention characteristics, using aqueous-acetonitrile mobile phases containing either formic acid (FA), ammonium formate (AF) or phosphoric acid (PA). The effect of organic solvent concentration on the results was also studied. Peak shape was good for neutrals under most mobile phase conditions. However, peak shapes for ionised solutes, particularly for basic compounds, were considerably worse in FA than AF. Even neutral compounds showed deterioration in performance with FA when the mobile phase water concentration was reduced. The poor performance in FA cannot be entirely attributed to the negative impact of ionic retention on ionised silanols on the underlying silica base materials, as results using PA at lower pH (where their ionisation is suppressed) were inferior to those in AF. Besides the moderating influence of the salt cation on ionic retention, it is likely that salt buffers improve peak shape due to the increased ionic strength of the mobile phase and its impact on the formation of the water layer on the column surface. PMID:24813934

  8. Enhanced development of lacustrine microbialites on gravity flow deposits, Great Salt Lake, Utah, USA

    NASA Astrophysics Data System (ADS)

    Bouton, Anthony; Vennin, Emmanuelle; Mulder, Thierry; Pace, Aurélie; Bourillot, Raphaël; Thomazo, Christophe; Brayard, Arnaud; Goslar, Tomasz; Buoncristiani, Jean-François; Désaubliaux, Guy; Visscher, Pieter T.

    2016-07-01

    The Great Salt Lake, Utah, USA is a shallow, hypersaline, intracontinental lake hosting extensive microbial deposits. At a large spatial scale, the distribution of these deposits is driven by environmental and geodynamical factors (i.e. water-level fluctuations and a fault-related framework). A detailed mapping of the Buffalo Point area, in the north-western part of Antelope Island, indicates the presence of an anomalous concentration of microbial deposits dated ca. 5.8 ka BP and distributed along a lobe-shaped geometry. This uncommon microbial deposit geometry results from an extensive colonization of a conglomerate substrate exhibiting an accumulation of m-sized rounded Cambrian quartzite boulders. We suggest that this conglomerate substrate provides a stable nucleation point that promotes the development and preservation of the lobe-shaped microbial deposits. Microbial deposits may also have protected the conglomerate substrate from erosional processes and thereby increased the preservation potential of the lobe-shaped structure. Based on the characteristics of the conglomerate (e.g. grain size, texture) and its location (i.e. 200 m beyond the average shoreline), this lobe-shaped structure likely results from subaqueous debris or a hyperconcentrated density flow that transports sedimentary material from the Buffalo Point slopes downward to the shore. We estimate the age of the conglomerate deposition to be between 21 and 12 ka BP. The initiation of the flow may have been triggered by various mechanisms, but the existence of a major active normal fault in the vicinity of these deposits suggests that an earthquake could have destabilized the accumulated sediments and resulted in conglomerate emplacement. The catastrophic 15 ka BP Bonneville Flood, which led to a drop in the lake level (approximately 110 m), may also provide an explanation for the initiation of the flow.

  9. Salicylic Acid Improved In Viro Meristem Regeneration and Salt Tolerance in Two Hibiscus Species

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Salicylic acid (SA) has been reported to induce abiotic stress, including salt tolerance in plants. The objective of this study was to determine whether application of various exogenous SA concentrations to in vitro grown meristem shoots could induce salt tolerance in two Hibiscus species. The effec...

  10. 40 CFR 721.4663 - Fluorinated carboxylic acid alkali metal salts.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... metal salts. 721.4663 Section 721.4663 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.4663 Fluorinated carboxylic acid alkali metal salts. (a)...

  11. EMISSION INVENTORY APPLICATIONS TO REGIONAL ACID DEPOSITION MODELING

    EPA Science Inventory

    A comprehensive Regional Acid Deposition Model (RADM) is being developed and a simpler fast-turn-around 'engineering' model(s) (EM) is being designed by the National Center for Atmospheric Research as part of the National Acid Precipitation Assessment Program (NAPAP). This paper ...

  12. ANTHROPOGENIC EMISSIONS INVOLVED IN ACIDIC DEPOSITION PROCESSES

    EPA Science Inventory

    The paper describes the methodology that was used to develop the 1985 National Acid Precipitation Assessment Program (NAPAP) Emissions Inventory, including quality control procedures. and summarizes the inventory contents. evelopment of the 1985 inventory required detailed invest...

  13. Salt and acid studies on canine lingual epithelium.

    PubMed

    Simon, S A; Garvin, J L

    1985-11-01

    A section of dog tongue just anterior to the circumvallate papillae was placed in an Ussing chamber and characterized with respect to monovalent cation transport pathways, response to HCl, and the interaction between salt and acid for the purposes of determining whether ion transport through the tongue is related to the transduction process. The primary findings of this work follow. The stimulation of the short-circuit current (Isc) with decreasing pH on the dorsal surface results from a net Cl- efflux through an amiloride- and ouabain-insensitive pathway that changed its selectivity from cationic at neutral pH to anionic at lower pH values. The stimulation is abolished at isotonic NaCl concentrations. This behavior would not be predicted from the proton-binding model to a "sour receptor" as suggested by Beidler (Handbook of Sensory Physiology; Berlin: Springer-Verlag, 1971). In symmetrical solutions of Krebs-Henseleit buffer, Isc is inhibited 30% by 10(-4) M amiloride on the mucosal side and 100% by 10(-3) M ouabain on the serosal side. These results coupled with net Cl- and Na+ flux measurements show that Isc is due to a net Cl- efflux. With 1.0 M NaCl on the dorsal side, 10(-4) M amiloride inhibits Isc 84%. In contrast, when the mucosal surface is bathed in KCl (1.0 M), CsCl (1.0 M), or HCl (10(-3) M), Isc is insensitive to both 10(-4) M amiloride and/or 10(-3) M ouabain. These data suggest that K+, Cs+, and H+ traverse the tongue through different pathways from Na+ and are not energized by a Na+ gradient. PMID:4061627

  14. National uranium resource evaluation. Geology and recognition criteria for sandstone uranium deposits of the salt wash type, Colorado Plateau Province. Final report

    SciTech Connect

    Thamm, J.K.; Kovschak, A.A. Jr.; Adams, S.S.

    1981-01-01

    The uranium-vanadium deposits of the Salt Wash Member of the Morrison Formation in the Colorado Plateau are similar to sandstone uranium deposits elsewhere in the USA. The differences between Salt Wash deposits and other sandstone uranium deposits are also significant. The Salt Wash deposits are unique among sandstone deposits in that they are dominantly vanadium deposits with accessory uranium. The Salt Wash ores generally occur entirely within reduced sandstone, without adjacent tongues of oxidized sandstone. They are more like the deposits of Grants, which similarly occur in reduced sandstones. Recent studies of the Grants deposits have identified alteration assemblages which are asymmetrically distributed about the deposits and provide a basis for a genetic model for those deposits. The alteration types recognized by Shawe in the Slick Rock district may provide similar constraints on ore formation when expanded to broader areas and more complete chemical analyses.

  15. 40 CFR 721.10630 - Amino acid, carboxyalkyl, alkylsulfonate, alkali salt (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Amino acid, carboxyalkyl... Significant New Uses for Specific Chemical Substances § 721.10630 Amino acid, carboxyalkyl, alkylsulfonate... chemical substances identified generically as amino acid, carboxyalkyl, alkylsulfonate, alkali salts...

  16. 40 CFR 721.10630 - Amino acid, carboxyalkyl, alkylsulfonate, alkali salt (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Amino acid, carboxyalkyl... Significant New Uses for Specific Chemical Substances § 721.10630 Amino acid, carboxyalkyl, alkylsulfonate... chemical substances identified generically as amino acid, carboxyalkyl, alkylsulfonate, alkali salts...

  17. ACID PRECIPITATION IN NORTH AMERICA: 1984 ANNUAL DATA SUMMARY FROM ACID DEPOSITION SYSTEM DATA BASE

    EPA Science Inventory

    The report gives a summary of 1984 wet deposition precipitation chemistry data collected in North America and available in the Acid Deposition System (ADS) data base. North American wet deposition monitoring networks with data in ADS are NADP/NTN, CANSAP, APN, UAPSP, MAP3S/PCN, W...

  18. ACID PRECIPITATION IN NORTH AMERICA: 1983 ANNUAL DATA SUMMARY FROM ACID DEPOSITION SYSTEM DATA BASE

    EPA Science Inventory

    The report gives a summary of 1983 wet deposition precipitation chemistry data collected in North America and available in the Acid Deposition System (ADS) data base. North American wet deposition monitoring networks with data in ADS are NADP/NTN, CANSAP, APN, UAPSP, MAP3S/PCN, W...

  19. Reaction of /alpha/,/beta/-unsaturated acyl isothiocyanates with salts of dithiocarbamic acids

    SciTech Connect

    Krus, K.; Masias, A.; Beletskaya, I.P.

    1989-01-10

    The reaction of unsaturated isothiocyanates with the sodium and calcium salts of N-alkyl- and N,N-dialkyldithiocarbamic acids was studied. Depending on the structure of the dithiocarbamate, the reaction products are thiazines or acyl dithiocarbamates. For the salts of methyldithiocarbamic acid the effect of the concentration and the nature of the metal on the relative yields of 6-phenyl-3-methylpropiorhodanine and 6-phenylpropiorhodanine was studied. A method is proposed for the synthesis of 3-substituted propiorhodanines.

  20. The distribution, structure, and composition of freshwater ice deposits in Bolivian salt lakes

    USGS Publications Warehouse

    Hurlbert, S.H.; Chang, Cecily C.Y.

    1988-01-01

    Freshwater ice deposits are described from seven, high elevation (4117-4730 m), shallow (mean depth <30 cm), saline (10-103 g l-1) lakes in the southwestern corner of Bolivia. The ice deposits range to several hundred meters in length and to 7 m in height above the lake or playa surface. They are located near the lake or salar margins; some are completely surrounded by water, others by playa deposits or salt crusts. Upper surfaces and sides of the ice deposits usually are covered by 20-40 cm of white to light brown, dry sedimentary materials. Calcite is the dominant crystalline mineral in these, and amorphous materials such as diatom frustules and volcanic glass are also often abundant. Beneath the dry overburden the ice occurs primarily as horizontal lenses 1-1000 mm thick, irregularly alternating with strata of frozen sedimentary materials. Ice represents from 10 to 87% of the volume of the deposits and yields freshwater (TFR <3 g l-1) when melted. Oxygen isotope ratios for ice are similar to those for regional precipitation and shoreline seeps but much lower than those for the lakewaters. Geothermal flux is high in the region as evidenced by numerous hot springs and deep (3.0-3.5 m) sediment temperatures of 5-10??C. This flux is one cause of the present gradual wasting away of these deposits. Mean annual air temperatures for the different lakes probably are all in the range of -2 to 4??C, and mean midwinter temperatures about 5??C lower. These deposits apparently formed during colder climatic conditions by the freezing of low salinity porewaters and the building up of segregation ice lenses. ?? 1988 Dr W. Junk Publishers.

  1. Microbial colonization of the salt deposits in the driest place of the Atacama Desert (Chile).

    PubMed

    Stivaletta, Nunzia; Barbieri, Roberto; Billi, Daniela

    2012-06-01

    The Atacama Desert (Chile), one of the most arid places on Earth, shows hostile conditions for the development of epilithic microbial communities. In this study, we report the association of cyanobacteria (Chroococcidiopsis sp.) and bacteria belonging to Actinobacteria and Beta-Gammaproteobacteria and Firmicutes phyla inhabiting the near surface of salt (halite) deposits of the Salar Grande Basin, Atacama Desert (Chile). The halite deposits were investigated by using optical, confocal and field emission scanning electron microscopes, whereas culture-independent molecular techniques, 16S rDNA clone library, alongside RFLP analysis and 16S rRNA gene sequencing were applied to investigate the bacterial diversity. These microbial communities are an example of life that has adapted to extreme environmental conditions caused by dryness, high irradiation, and metal concentrations. Their adaptation is, therefore, important in the investigation of the environmental conditions that might be expected for life outside of Earth. PMID:22661023

  2. Effect of root metabolism on the post-depositional mobilization of mercury in salt marsh soils

    SciTech Connect

    Marins, R.V. |; Lacerda, L.D.; Goncalves, G.O.; Paiva, E.C. de

    1997-05-01

    Salt marsh soils are an efficient sink for trace metals associated with particulate material in tidal waters and have been proposed as monitors for trace metal contamination in coastal areas, on the basis that vertical profiles provide a record of loading rates. However, the complex nature of the biogeochemical processes occurring in these soils, may prevent this use, since post-depositional mobilization of some trace metals may occur, resulting in their release to pore water, vertical movement through the soil column and exchange with overlying waters. This paper presents and compares the vertical profiles of mercury in soil cores taken under a Spartina altermilflora marsh and in adjacent mod flats without plant cover to characterize the role played by this plant on the post-depositional movement of mercury through the soil and on the possibility of using such profiles as indicators of mercury loading rates in coastal areas. 19 refs., 1 fig., 1 tab.

  3. Microbial Colonization of the Salt Deposits in the Driest Place of the Atacama Desert (Chile)

    NASA Astrophysics Data System (ADS)

    Stivaletta, Nunzia; Barbieri, Roberto; Billi, Daniela

    2012-06-01

    The Atacama Desert (Chile), one of the most arid places on Earth, shows hostile conditions for the development of epilithic microbial communities. In this study, we report the association of cyanobacteria ( Chroococcidiopsis sp.) and bacteria belonging to Actinobacteria and Beta-Gammaproteobacteria and Firmicutes phyla inhabiting the near surface of salt (halite) deposits of the Salar Grande Basin, Atacama Desert (Chile). The halite deposits were investigated by using optical, confocal and field emission scanning electron microscopes, whereas culture-independent molecular techniques, 16S rDNA clone library, alongside RFLP analysis and 16S rRNA gene sequencing were applied to investigate the bacterial diversity. These microbial communities are an example of life that has adapted to extreme environmental conditions caused by dryness, high irradiation, and metal concentrations. Their adaptation is, therefore, important in the investigation of the environmental conditions that might be expected for life outside of Earth.

  4. Transition-metal salt-containing silica nanocapsules elaborated via salt-induced interfacial deposition in inverse miniemulsions as precursor to functional hollow silica particles.

    PubMed

    Cao, Zhihai; Yang, Liu; Ye, Quanlin; Cui, Qinmin; Qi, Dongming; Ziener, Ulrich

    2013-06-01

    Aqueous core-silica shell nanocapsules were successfully prepared using liquid droplets containing transition-metal salt as templates in inverse miniemulsions. The formation of the silica shell was attributed to the interfacial deposition of silica species induced by the presence of the transition-metal salt. In addition to the control of the particle morphology, the incorporated transition-metal salts could be used to derivatize the particles and confer additional functionalities to the hollow silica particles. To demonstrate the derivatization, the magnetic hollow silica particles were prepared by converting iron salts to magnetic iron oxides by heat treatment. The particle morphology, size, and size distribution were characterized by transmission electron microscopy and scanning electron microscopy. The results show that the particle properties strongly depend on the type and the amount of salts, the amount of tetraethoxysilane (TEOS), the pH of the droplets, and the ratios of 2-hydroxyethyl methacrylate to aqueous HCl solution. The specific surface area and pore properties were characterized by N2 sorption measurements. The pore properties and specific surface area could be tuned by varying the amount of salt. Levels of elements and of iron oxides in the magnetic hollow particles were measured by energy-dispersive X-ray spectroscopy. Iron was distributed homogenously with silicon and oxygen in the sample. The magnetization measured by a magnetic property measurement system confirmed the successful conversion of the iron salts to magnetic iron oxides. PMID:23679054

  5. Structure of eight molecular salts assembled from noncovalent bonding between carboxylic acids, imidazole, and benzimidazole

    NASA Astrophysics Data System (ADS)

    Jin, Shouwen; Zhang, Huan; Liu, Hui; Wen, Xianhong; Li, Minghui; Wang, Daqi

    2015-09-01

    Eight organic salts of imidazole/benzimidazole have been prepared with carboxylic acids as 2-methyl-2-phenoxypropanoic acid, α-ketoglutaric acid, 5-nitrosalicylic acid, isophthalic acid, 4-nitro-phthalic acid, and 3,5-dinitrosalicylic acid. The eight crystalline forms reported are proton-transfer compounds of which the crystals and compounds were characterized by X-ray diffraction analysis, IR, mp, and elemental analysis. These structures adopted hetero supramolecular synthons, with the most common R22(7) motif observed at salts 2, 3, 5, 6 and 8. Analysis of the crystal packing of 1-8 suggests that there are extensive strong Nsbnd H⋯O, and Osbnd H⋯O hydrogen bonds (charge assisted or neutral) between acid and imidazolyl components in all of the salts. Except the classical hydrogen bonding interactions, the secondary propagating interactions also play important roles in structure extension. This variety, coupled with the varying geometries and number of acidic groups of the acids utilized, has led to the creation of eight supramolecular arrays with 1D-3D structure. The role of weak and strong noncovalent interactions in the crystal packing is analyzed. The results presented herein indicate that the strength and directionality of the Nsbnd H⋯O, and Osbnd H⋯O hydrogen bonds between acids and imidazole/benzimidazole are sufficient to bring about the formation of organic salts.

  6. Halococcus dombrowskii sp. nov., an archaeal isolate from a Permian alpine salt deposit.

    PubMed

    Stan-Lotter, Helga; Pfaffenhuemer, Marion; Legat, Andrea; Busse, Hans-Jürgen; Radax, Christian; Gruber, Claudia

    2002-09-01

    Several extremely halophilic coccoid archaeal strains were isolated from pieces of dry rock salt that were obtained three days after blasting operations in an Austrian salt mine. The deposition of the salt is thought to have occurred during the Permian period (225-280 million years ago). On the basis of their polar-lipid composition, 16S rRNA gene sequences, cell shape and growth characteristics, the isolates were assigned to the genus Halococcus. The DNA-DNA reassociation values of one isolate, strain H4T, were 35 and 38% with Halococcus salifodinae and Halococcus saccharolyticus, respectively, and 65.8-67.8% with Halococcus morrhuae. The polar lipids of strain H4T were C20-C25 derivatives of phosphatidylglycerol and phosphatidylglycerol phosphate. Whole-cell protein patterns, menaquinone content, enzyme composition, arrangements of cells, usage of carbon and energy sources, and antibiotic susceptibility were sufficiently different between strain H4T and H. morrhuae to warrant designation of strain H4T as a new species within the genus Halococcus. It is proposed that the isolate be named Halococcus dombrowskii, and the type strain is H4T (= DSM 14522T = NCIMB 13803T = ATCC BAA-364T). PMID:12361290

  7. Improved Proteome and Phosphoproteome Analysis on a Cation Exchanger by a Combined Acid and Salt Gradient.

    PubMed

    Adachi, Jun; Hashiguchi, Kazunari; Nagano, Maiko; Sato, Misako; Sato, Ayako; Fukamizu, Kazuna; Ishihama, Yasushi; Tomonaga, Takeshi

    2016-08-16

    Currently used elution methods for strong cation exchange (SCX) chromatography are based on two principles: salt and pH gradient. In this paper, we report the first observation of peptide elution by acid gradient. The degree of peptide separation using C18-SCX StageTip was greatly improved by our acid and salt-based elution method compared with a salt-based elution method. This development enabled us to identify over 22 000 phosphopeptides from 2 mg of protein without labor-intensive sample preparation. Our method is simple, robust, scalable, and low-cost and can be easily implemented without any special equipment or techniques. PMID:27436111

  8. Investigation of evaporate deposits in the “Great Ear” area of Lop Nor salt plain, Xinjiang Province, China

    NASA Astrophysics Data System (ADS)

    Ma, L.; Li, B.; Jiang, P.; Lowenstein, T. K.; Zhong, J.; Sheng, J.; Wu, H.

    2009-12-01

    In arid regions of the world, salt pans are common features occupying the lowest areas of closed interior basin. The Lop Nor salt plain is located at the east end of the Tarim Basin, Xinjiang Province, China. Widespread Holocene salt deposits were known to cover thousands of square kilometers and up to hundreds of meters thick. However, the salt pans in the central-eastern sector of the Lop Nor salt plain is unusually represented by successive concentric black-and-white rings that closely resembled a big human ear in satellite images. The total area of the “Great Ear” is approximately 5,500 km2, and the internal morphology is considered essentially flat with an elevation of 800 m. A series of detailed field investigations on the “Great Ear” salt pans involved describing evaporates and surface morphologies, measuring chemical compositions, and groundwater depths. The deposits show clear lateral variations in salt content, water content, evaporate mineralogy, as well as the microrelief of salt crust in the “Great Ear” area. Spatially, spectral imaging variation corresponds to color variation in the “Great Ear”, which suggests surface moist conditions of a salt pan: dark-toned areas are wet and the bright-toned areas are dry. In the wet zone, capillary fringing of groundwater brines control the precipitation of evaporites and microrelief genesis. The salt pans are marked by pressure-ridge and well-developed hexagonal honeycomb polygons structures, where the microrelief of salt crust ranges from 30 to 80 cm. In the dry salt pans zone, groundwater discharge was not observed on the surface and the salt crust is characterized by low relief, low salinity, a lack of efflorescences crusts, and significant amounts of detrital sediments. This zone shows bright-tone in the satellite images due to higher reflectance of dry salt-encrusted pans surface. Though, the sediment beneath the surface typically is saturated with concentrated brines and displacive

  9. Quality and quantity of runoff and atmospheric deposition in urban areas of Salt Lake County, Utah, 1980-81

    USGS Publications Warehouse

    Christensen, R.C.; Stephens, D.W.; Pyper, G.E.; McCormack, H.F.; Weigel, J.F.

    1984-01-01

    Water of good quality from mountain streams is degraded as it moves through urban areas to the Jordan River in Salt Lake County, Utah. The impact of urban runoff and atmospheric deposition on the quality of water in those streams and in storm conduits and canals functioning as storm drains was evaluated using data collected during 1980-81. Atmospheric-wetfall loads for an average storm were as much as 10 pounds per acre for total solids, but the dissolved trace metals were generally present in insignificant quantities. Wetfall-deposition loads generally were greater than storm-runoff loads, indicating that a large quantity of the wetfall load remained as soil deposits. Acid rain fell in more than one-half of the storms sampled, most commonly in September and October. Dustfall concentrations reflected the composition of local soils, particularly with regard to iron, manganese, and chromium; but concentrations of cadmium, copper, lead, zinc, and chloride were considerably enriched. Monthly loads of dryfall solids reached a maximum of 62 pounds per acre in the Little Cottonwood Creek urban basin, but were of the same magnitude as total storm loads for a heavy rainfall. Urban runoff represented about 38 percent of the discharge in three canals. The water in the canals was poorer in quality than the water in the mountain streams. The impact of the canal discharges to the streams is slight, however, owing to their ' relatively small amounts. ' Concentrations of sediment, suspended solids, suspended trace metals, phosphorus, and oxygen-demanding substances were much greater during storm runoff than under base-flow conditions. This report contains data for basin and storm characteristics and water-quality information for atmospheric deposition and urban runoff. (USGS)

  10. Enhanced skin permeation of 6-methoxy-2-naphthylacetic acid by salt formation.

    PubMed

    Pawar, Vijay; Kumar, H Yogish; Giridhar, Rajani; Yadav, Mange Ram

    2015-05-01

    The aim of this work was to prepare salts of 6-methoxy-2-naphthylacetic acid (6-MNA) to improve its physicochemical properties for percutaneous application. 6-MNA, an active metabolite of non-steroidal anti-inflammatory drug nabumetone has long half life and has the tendency to penetrate well into synovial fluid. The physicochemical properties of 6-MNA salts were investigated by solubility measurements, differential scanning calorimetry (DSC) and infrared (IR). The DSC thermograms and Fourier transform infrared (FT-IR) spectra indicated that 6-MNA formed salts with organic and alkali metal bases. Among the series, salts formed with amine bases (ethanolamine, diethanolamine, triethanolamine and diethylamine) had lower melting points while alkali metal salt (sodium) had higher melting point than 6-MNA. The salts had higher solubilities than 6-MNA as determined in phosphate buffer at pH 5.0 and 7.4. There is no significant difference in partition coefficient (log P) values between salts and 6-MNA at pH 5.0 but, at pH 7.4, the log P values for the salts increased by 4-10 times as compared to 6-MNA. In vitro permeation studies showed that all the salts increased the flux in comparision to 6-MNA, and the ethanolamine salt (1b) was found to be having 7.7 and 9.4 times higher permeability as compared to 6-MNA at pH 5.0 and 7.4, respectively. PMID:24670100

  11. Atmospheric salt deposition in a tropical mountain rainforest at the eastern Andean slopes of south Ecuador - Pacific or Atlantic origin?

    NASA Astrophysics Data System (ADS)

    Makowski Giannoni, Sandro; Trachte, Katja; Rollenbeck, Ruetger; Lehnert, Lukas; Fuchs, Julia; Bendix, Joerg

    2016-08-01

    Sea salt (NaCl) has recently been proven to be of the utmost importance for ecosystem functioning in Amazon lowland forests because of its impact on herbivory, litter decomposition and, thus, carbon cycling. Sea salt deposition should generally decline as distance from its marine source increases. For the Amazon, a negative east-west gradient of sea salt availability is assumed as a consequence of the barrier effect of the Andes Mountains for Pacific air masses. However, this generalized pattern may not hold for the tropical mountain rainforest in the Andes of southern Ecuador. To analyse sea salt availability, we investigated the deposition of sodium (Na+) and chloride (Cl-), which are good proxies of sea spray aerosol. Because of the complexity of the terrain and related cloud and rain formation processes, sea salt deposition was analysed from both, rain and occult precipitation (OP) along an altitudinal gradient over a period between 2004 and 2009. To assess the influence of easterly and westerly air masses on the deposition of sodium and chloride over southern Ecuador, sea salt aerosol concentration data from the Monitoring Atmospheric Composition and Climate (MACC) reanalysis data set and back-trajectory statistical methods were combined. Our results, based on deposition time series, show a clear difference in the temporal variation of sodium and chloride concentration and Na+ / Cl- ratio in relation to height and exposure to winds. At higher elevations, sodium and chloride present a higher seasonality and the Na+ / Cl- ratio is closer to that of sea salt. Medium- to long-range sea salt transport exhibited a similar seasonality, which shows the link between our measurements at high elevations and the sea salt synoptic transport. Although the influence of the easterlies was predominant regarding the atmospheric circulation, the statistical analysis of trajectories and hybrid receptor models revealed a stronger impact of the north equatorial Atlantic, Caribbean

  12. A mechanistic study of phosphinocarboxylic acid for boiler deposit control

    SciTech Connect

    Chang, K.Y.; Patel, S.

    1995-11-01

    A laboratory study has been carried out to identify the key properties of phosphinocarboxylic acid polymers to control boiler water deposits. These multifunctional properties are its ability to: transport iron, disperse boiler water sludge that contains iron oxide, silica and calcium phosphate and dissolution of deposits. The thermal and hydrolytic stability of the phosphinocarboxylic acid polymers was investigated in autoclave studies up to 1,500 psig. The post-autoclave samples were analyzed by Nuclear Magnetic Resonance Spectroscopy and Aqueous Gel Permeation Chromatography to ascertain the polymer integrity. In addition performance tests were carried out for pre- and post-autoclave polymer samples. The performance testing clearly shows that phosphinocarboxylic acid polymers are effective in maintaining deposit control in a boiler due to their inherent thermal stability.

  13. Deposition of Na2SO4 from salt-seeded combustion gases of a high velocity burner rig

    NASA Astrophysics Data System (ADS)

    Santoro, G. J.; Gokoglu, S. A.; Kohl, F. J.; Stearns, C. A.; Rosner, D. E.

    The mechanism of deposition of Na2SO4 was studied under controlled laboratory conditions and the results have been compared to a recently developed comprehensive theory of vapor deposition. Thus Na2SO4, NaCl, NaNO3 and simulated sea salt solutions were injected into the combustor of a nominal Mach 0.3 burner rig burning jet fuel at constant fuel/air ratios. The deposits formed on inert collectors, rotation in the cross flow of the combustion gases, were weighed and analyzed. Collector temperature was uniform and could be varied over a large range by internal air cooling. Deposition rates and dew point temperatures were determined. Supplemental testing included droplet size measurements of the atomized salt solutions. These tests along with thermodynamic and transport calculations were utilized in the interpretation of the deposition results.

  14. Deposition of Na2SO4 from salt-seeded combustion gases of a high velocity burner rig

    NASA Technical Reports Server (NTRS)

    Santoro, G. J.; Gokoglu, S. A.; Kohl, F. J.; Stearns, C. A.; Rosner, D. E.

    1984-01-01

    The mechanism of deposition of Na2SO4 was studied under controlled laboratory conditions and the results have been compared to a recently developed comprehensive theory of vapor deposition. Thus Na2SO4, NaCl, NaNO3 and simulated sea salt solutions were injected into the combustor of a nominal Mach 0.3 burner rig burning jet fuel at constant fuel/air ratios. The deposits formed on inert collectors, rotation in the cross flow of the combustion gases, were weighed and analyzed. Collector temperature was uniform and could be varied over a large range by internal air cooling. Deposition rates and dew point temperatures were determined. Supplemental testing included droplet size measurements of the atomized salt solutions. These tests along with thermodynamic and transport calculations were utilized in the interpretation of the deposition results.

  15. Nitrooleic Acid Attenuates Lipid Metabolic Disorders and Liver Steatosis in DOCA-Salt Hypertensive Mice

    PubMed Central

    Sun, Jing; Jia, Zhanjun; Yang, Tianxin; Xu, Liang; Zhao, Bing; Yu, Kezhou; Wang, Rong

    2015-01-01

    Nitrooleic acid (OA-NO2) is endogenous ligands for peroxisome proliferator-activated receptors. The present study was aimed at investigating the beneficial effects of OA-NO2 on the lipid metabolism and liver steatosis in deoxycorticosterone acetate- (DOCA-) salt induced hypertensive mice model. Male C57BL/6 mice were divided to receive DOCA-salt plus OA-NO2 or DOCA-salt plus vehicle and another group received neither DOCA-salt nor OA-NO2 (control group). After 3-week treatment with DOCA-salt plus 1% sodium chloride in drinking fluid, the hypertension was noted; however, OA-NO2 had no effect on the hypertension. In DOCA-salt treated mice, the plasma triglyceride and total cholesterol levels were significantly increased compared to control mice, and pretreatment with OA-NO2 significantly reduced these parameters. Further, the histopathology of liver exhibited more lipid distribution together with more serious micro- and macrovesicular steatosis after DOCA-salt treatment and that was consistent with liver tissue triglyceride and nonesterified fatty acids (NEFA) content. The mice pretreated with OA-NO2 showed reduced liver damage accompanied with low liver lipid content. Moreover, the liver TBARS, together with the expressions of gp91phox and p47phox, were parallelly decreased. These findings indicated that OA-NO2 had the protective effect on liver injury against DOCA-salt administration and the beneficial effect could be attributed to its antihyperlipidemic activities. PMID:25861250

  16. Deposition of Na2SO4 from salt-seeded combustion gases of a high velocity burner rig

    NASA Technical Reports Server (NTRS)

    Santoro, G. J.; Kohl, F. J.; Stearns, C. A.; Gokoglu, S. A.; Rosner, D. A.

    1985-01-01

    With a view to developing simulation criteria for the laboratory testing of high-temperature materials for gas turbine engines, the deposition rates of sodium sulfate from sodium salt-seeded combustion gases were determined experimentally using a well instrumented high-velocity burner. In the experiments, Na2SO4, NaCl, NaNO3, and simulated sea salt solutions were injected into the combustor of the Mach 0.3 burner rig operating at constant fuel/air ratios. The deposits formed on an inert rotating collector were then weighed and analyzed. The experimental results are compared to Rosner's vapor diffusion theory. Some additional test results, including droplet size distribution of an atomized salt spray, are used in interpreting the deposition rate data.

  17. The interpretation of digital recordings of SIR-A, Seasat, and Landsat data of the Algerian salt deposits

    NASA Technical Reports Server (NTRS)

    Rebillard, P.; Ballais, J.-P.

    1983-01-01

    Seasat and SIR-A SAR and Landsat MSS imagery of the salt beds of western Algeria are compared. The Landsat image was made 5 yr before the Seasat image, which was taken nearly 9 yr before the Shuttle radar image. The latter was processed in the visible channel. Differences in the backscatter in the radar imagery are attributed to the viewing angle and the characteristics of each salt deposit. The imagery allowed a determination of the changes in the shapes and areal extent of the salt pools over time, as well as alterations in nearby vegetation cover and the evolution of aeolian formations.

  18. Modeling wet deposition of acid substances over the PRD region in China

    NASA Astrophysics Data System (ADS)

    Lu, Xingcheng; Fung, Jimmy Chi Hung; Wu, Dongwei

    2015-12-01

    The Pearl River Delta (PRD) region in southern China has suffered heavily from acid rain in the last 10 years due to the anthropogenic emission of sulfur dioxide and nitrogen dioxide. Several measurement-based studies about this issue have been conducted to analyze the chemical composition of precipitation in this area. However, no detailed, high resolution numerical simulation regarding this topic has ever been done in this region. In this study, the WRF-SMOKE-CMAQ system was applied to simulate the wet deposition of acid substances (SO42- and NO3-) in the PRD region from 2009 to 2011 with a resolution of 3 km. The simulation output agreed well with the observation data. Our results showed that Guangzhou was the city most affected by acid rain in this region. The ratio of non-sea-salt sulfate to nitrate indicated that the acid rain in this region belonged to the sulfate-nitrate mixed type. The source apportionment result suggests that point source and super regional source are the ones that contribute the pollutants most in the rain water over PRD Region. The sulfate and nitrate input to some reservoirs via wet deposition was also estimated based on the model simulation. Our results suggest that further cross-city cooperation and emission reduction are needed to further curb acid rain in this region.

  19. Spatial and Temporal Characteristics of Insulator Contaminations Revealed by Daily Observations of Equivalent Salt Deposit Density

    PubMed Central

    Ruan, Ling; Han, Ge; Zhu, Zhongmin; Zhang, Miao; Gong, Wei

    2015-01-01

    The accurate estimation of deposits adhering on insulators is of great significance to prevent pollution flashovers which cause huge costs worldwide. Researchers have developed sensors using different technologies to monitor insulator contamination on a fine time scale. However, there is lack of analysis of these data to reveal spatial and temporal characteristics of insulator contamination, and as a result the scheduling of periodical maintenance of power facilities is highly dependent on personal experience. Owing to the deployment of novel sensors, daily Equivalent Salt Deposit Density (ESDD) observations of over two years were collected and analyzed for the first time. Results from 16 sites distributed in four regions of Hubei demonstrated that spatial heterogeneity can be seen at both the fine and coarse geographical scales, suggesting that current polluted area maps are necessary but are not sufficient conditions to guide the maintenance of power facilities. Both the local emission and the regional air pollution condition exert evident influences on deposit accumulation. A relationship between ESDD and PM10 was revealed by using regression analysis, proving that air pollution exerts influence on pollution accumulations on insulators. Moreover, the seasonality of ESDD was discovered for the first time by means of time series analysis, which could help engineers select appropriate times to clean the contamination. Besides, the trend component shows that the ESDD increases in a negative exponential fashion with the accumulation date (ESDD = a − b × exp(−time)) at a long time scale in real environments. PMID:25643058

  20. Closed cycle ion exchange method for regenerating acids, bases and salts

    DOEpatents

    Dreyfuss, Robert M.

    1976-01-01

    A method for conducting a chemical reaction in acidic, basic, or neutral solution as required and then regenerating the acid, base, or salt by means of ion exchange in a closed cycle reaction sequence which comprises contacting the spent acid, base, or salt with an ion exchanger, preferably a synthetic organic ion-exchange resin, so selected that the counter ions thereof are ions also produced as a by-product in the closed reaction cycle, and then regenerating the spent ion exchanger by contact with the by-product counter ions. The method is particularly applicable to closed cycle processes for the thermochemical production of hydrogen.

  1. General Synthesis of Amino Acid Salts from Amino Alcohols and Basic Water Liberating H2.

    PubMed

    Hu, Peng; Ben-David, Yehoshoa; Milstein, David

    2016-05-18

    An atom-economical and environmentally friendly method to transform amino alcohols to amino acid salts using just basic water, without the need of pre-protection or added oxidant, catalyzed by a ruthenium pincer complex, is developed. Water is the solvent, the source of the oxygen atom of the carboxylic acid group, and the actual oxidant, with liberation of dihydrogen. Many important and useful natural and unnatural amino acid salts can be produced in excellent yields by applying this new method. PMID:27139983

  2. 40 CFR 721.2098 - Aliphatic polycarboxylic acid metal salt (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... (CONTINUED) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.2098 Aliphatic polycarboxylic acid metal salt (generic). (a) Chemical... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Aliphatic polycarboxylic acid...

  3. 21 CFR 173.45 - Polymaleic acid and its sodium salt.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... method entitled “Determination of Molecular Weight Distribution of Poly(Maleic) Acid,” March 17, 1992... reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies are available from the Office of Food... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polymaleic acid and its sodium salt....

  4. 78 FR 64914 - Citric Acid and Certain Citrate Salts From Canada: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-10-30

    ... China: Antidumping Duty Orders, 74 FR 25703 (May 29, 2009) (Citric Acid Duty Orders). Period of Review...-others rate made effective by the LTFV investigation. See Citric Acid Duty Orders, 74 FR 25703. These... Salts from Canada: Preliminary Results of Antidumping Duty Administrative Review; 2011- 2012, 78...

  5. 40 CFR 721.3820 - L-Glutamic acid, N-(1-oxododecyl)-, disodium salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false L-Glutamic acid, N-(1-oxododecyl... Specific Chemical Substances § 721.3820 L-Glutamic acid, N-(1-oxododecyl)-, disodium salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as...

  6. 40 CFR 721.3820 - L-Glutamic acid, N-(1-oxododecyl)-, disodium salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false L-Glutamic acid, N-(1-oxododecyl... Specific Chemical Substances § 721.3820 L-Glutamic acid, N-(1-oxododecyl)-, disodium salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as...

  7. 76 FR 5782 - Citric Acid and Certain Citrate Salts From Canada: Preliminary Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-02-02

    ... Part, and Final Determination to Not Revoke Order in Part: Canned Pineapple Fruit from Thailand, 68 FR... Administrative Reviews and Requests for Revocation in Part, 75 FR 37759 (June 30, 2010). Also on June 30, 2010... Acid and Certain Citrate Salts from Canada, 74 FR 16843 (April 13, 2009) (Citric Acid LTFV)....

  8. Bactericidal activity of alkaline salts of fatty acids towards bacteria associated with poultry processing

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Antibacterial activity of alkaline salts of caproic, caprylic, capric, lauric, and myristic acids were determined using the agar diffusion assay. A 0.5M concentration of each fatty acid (FA) was dissolved in 1.0 M potassium hydroxide (KOH), and pH of the mixtures was adjusted to 10.5 with citric aci...

  9. Five organic salts assembled from carboxylic acids and bis-imidazole derivatives through collective noncovalent interactions

    NASA Astrophysics Data System (ADS)

    Jin, Shouwen; Guo, Jianzhong; Liu, Li; Wang, Daqi

    2011-10-01

    Five multicomponent crystals of bis(imidazole) derivatives have been prepared with 5-nitrosalicylic acid, 5-sulfosalicylic acid, and phthalic acid. The five crystalline forms reported are organic salts of which the crystal structures have all been determined by X-ray diffraction. The results presented herein indicate that the strength and directionality of the N sbnd H⋯O, O sbnd H⋯O, and N sbnd H⋯N hydrogen bonds (ionic or neutral) between carboxylic acids and ditopic imidazoles are sufficient to bring about the formation of binary organic salts. All supramolecular architectures of the organic salts 1- 5 involve extensive O sbnd H⋯O, and N sbnd H⋯O hydrogen bonds as well as other noncovalent interactions. The role of weak and strong noncovalent interactions in the crystal packing is ascertained. These noncovalent interactions combined, all the complexes displayed 3D framework structure.

  10. Phenolic acids as bioindicators of fly ash deposit revegetation.

    PubMed

    Djurdjević, L; Mitrović, M; Pavlović, P; Gajić, G; Kostić, O

    2006-05-01

    The floristic composition, the abundance, and the cover of pioneer plant species of spontaneously formed plant communities and the content of total phenolics and phenolic acids, as humus constituents, of an ash deposit after 7 years of recultivation were studied. The restoration of both the soil and the vegetation on the ash deposits of the "Nikola Tesla-A" thermoelectric power plant in Obrenovac (Serbia) is an extremely slow process. Unfavorable physical and chemical characteristics, the toxicity of fly ash, and extreme microclimatic conditions prevented the development of compact plant cover. The abundance and cover of plants increased from the central part of the deposit towards its edges (ranging from 1-80%). Festuca rubra L., Crepis setosa Hall., Erigeron canadensis L., Cirsium arvense (L.) Scop., Calamagrostis epigeios (L.) Roth., and Tamarix gallica L. were the most abundant species, thus giving the highest cover. Humus generated during the decomposition process of plant remains represents a completely new product absent in the ash as the starting material. The amount of total phenolics and phenolic acids (38.07-185.16 microg/g of total phenolics and 4.12-27.28 microg/g of phenolic acids) in fly ash increased from the center of the deposit towards its edges in correlation with the increase in plant abundance and cover. Ash samples contained high amounts of ferulic, vanillic, and p-coumaric acid, while the content of both p-hydroxybenzoic and syringic acid was relatively low. The presence of phenolic acids indicates the ongoing process of humus formation in the ash, in which the most abundant pioneer plants of spontaneously formed plant communities play the main role. Phenolic compounds can serve as reliable bioindicators in an assessment of the success of the recultivation process of thermoelectric power plants' ash deposits. PMID:16418890

  11. Solubility of the Sodium and Ammonium Salts of Oxalic Acid in Water with Ammonium Sulfate.

    PubMed

    Buttke, Lukas G; Schueller, Justin R; Pearson, Christian S; Beyer, Keith D

    2016-08-18

    The solubility of the sodium and ammonium salts of oxalic acid in water with ammonium sulfate present has been studied using differential scanning calorimetry, X-ray crystallography, and infrared spectroscopy. The crystals that form from aqueous mixtures of ammonium sulfate/sodium hydrogen oxalate were determined to be sodium hydrogen oxalate monohydrate under low ammonium sulfate conditions and ammonium hydrogen oxalate hemihydrate under high ammonium sulfate conditions. Crystals from aqueous mixtures of ammonium sulfate/sodium oxalate were determined to be ammonium oxalate monohydrate under moderate to high ammonium sulfate concentrations and sodium oxalate under low ammonium sulfate concentrations. It was also found that ammonium sulfate enhances the solubility of the sodium oxalate salts (salting in effect) and decreases the solubility of the ammonium oxalate salts (salting out effect). In addition, a partial phase diagram for the ammonium hydrogen oxalate/water system was determined. PMID:27482644

  12. Phenolic acids as bioindicators of fly ash deposit revegetation

    SciTech Connect

    L. Djurdjevic; M. Mitrovic; P. Pavlovic; G. Gajic; O. Kostic

    2006-05-15

    The floristic composition, the abundance, and the cover of pioneer plant species of spontaneously formed plant communities and the content of total phenolics and phenolic acids, as humus constituents, of an ash deposit after 7 years of recultivation were studied. The restoration of both the soil and the vegetation on the ash deposits of the 'Nikola Tesla-A' thermoelectric power plant in Obrenovac (Serbia) is an extremely slow process. Unfavorable physical and chemical characteristics, the toxicity of fly ash, and extreme microclimatic conditions prevented the development of compact plant cover. The abundance and cover of plants increased from the central part of the deposit towards its edges. Festuca rubra L., Crepis setosa Hall., Erigeron canadensis L., Cirsium arvense (L.) Scop., Calamagrostis epigeios (L.) Roth., and Tamarix gallica L. were the most abundant species, thus giving the highest cover. Humus generated during the decomposition process of plant remains represents a completely new product absent in the ash as the starting material. The amount of total phenolics and phenolic acids in fly ash increased from the center of the deposit towards its edges in correlation with the increase in plant abundance and cover. The presence of phenolic acids indicates the ongoing process of humus formation in the ash, in which the most abundant pioneer plants of spontaneously formed plant communities play the main role. Phenolic compounds can serve as reliable bioindicators in an assessment of the success of the recultivation process of thermoelectric power plants' ash deposits.

  13. Anthropogenically driven changes in chloride complicate interpretation of base cation trends in lakes recovering from acidic deposition.

    PubMed

    Rosfjord, Catherine H; Webster, Katherine E; Kahl, Jeffrey S; Norton, Stephen A; Fernandez, Ivan J; Herlihy, Alan T

    2007-11-15

    Declines in Ca and Mg in low ANC lakes recovering from acidic deposition are widespread across the northern hemisphere. We report overall increases between 1984 and 2004 in the concentrations of Ca + Mg and Cl in lakes representing the statistical population of nearly 4000 low ANC lakes in the northeast U.S. Increases in Cl occurred in nearly all lakes in urbanized southern New England, but only 18% of lakes in more remote Maine had Cl increases. This spatial pattern implicates road salt application as the major source of the increased Cl salts. Among the 48% of the lake population classified as salt-affected, the median changes in Cl (+133 microeq/L) and Ca + Mg (+47 microeq/ L) were large and positive in direction over the 20 years. However, in the unaffected lakes, Cl remained stable and Ca + Mg decreased (-3 microeq/L), consistent with reported long-term trends in base cations of acid-sensitive lakes. This discrepancy between the Cl groups suggests that changes in ion exchange processes in salt-affected watersheds have altered the geochemical cycling of Ca and Mg. One policy-relevant implication is that waters influenced by Cl salts complicate regional assessments of surface water recovery from "acid rain" related to the passage of the Clean Air Act. PMID:18075075

  14. PARAMETRIC METHODOLOGIES OF CLOUD VERTICAL TRANSPORT FOR ACID DEPOSITION MODELS

    EPA Science Inventory

    A CUmulus VENTing (CUVENT) cloud module has been developed that calculates the vertical flux of mass from the boundary layer to the cloud layer by an ensemble of nonprecipitating subgrid-scale air mass clouds. This model will be integrated into the Regional Acid Deposition Model ...

  15. POLLUTANT SAMPLER FOR MEASUREMENTS OF ATMOSPHERIC ACIDIC DRY DEPOSITION

    EPA Science Inventory

    An acidic pollutant sampler for dry deposition monitoring has been designed and evaluated in laboratory and field studies. The system, which is modular and simple to operate, samples gaseous HNO3, NH3, SO2 and NO2 and particulate SO4(-2), NO3(1-) and NH4(1+) and is made of Teflon...

  16. Molecular and physiological responses to abscisic acid and salts in roots of salt-sensitive and salt-tolerant Indica rice varieties.

    PubMed Central

    Moons, A; Bauw, G; Prinsen, E; Van Montagu, M; Van der Straeten, D

    1995-01-01

    The Indica rice (Oryza sativa L.) varieties Pokkali and Nona Bokra are well-known salt tolerance donors in classical breeding. In an attempt to understand the molecular basis of their tolerance, physiological and gene expression studies were initiated. The effect of abscisic acid (ABA) on total proteins in roots from 12-d-old seedlings of Pokkali, Nona Bokra, and the salt-sensitive cultivar Taichung N1 were analyzed on two-dimensional gels. The abundance of ABA-induced proteins was highest in the most tolerant variety, Pokkali. Three ABA-responsive proteins, present at different levels in roots from tolerant and sensitive varieties, were further characterized by partial amino acid analysis. A novel histidine-rich protein and two types of late embryogenesis abundant (LEA) proteins were identified. Protein immunoblotting revealed that the levels of dehydrins and group 3 LEA proteins were significantly higher in roots from tolerant compared with sensitive varieties. Endogenous ABA levels showed a transient increase in roots exposed to osmotic shock (150 mM NaCl). Peak ABA concentrations were 30-fold higher for Nona Bokra and 6-fold higher for Pokkali compared with Taichung N1. Both the salt-induced endogenous ABA levels and a greater molecular response of root tissue to ABA were associated with the varietal differences in tolerance. PMID:7870812

  17. High temperature reaction between sea salt deposit and (U,Zr)O2 simulated corium debris

    NASA Astrophysics Data System (ADS)

    Takano, Masahide; Nishi, Tsuyoshi

    2013-11-01

    In order to clarify the possible impacts of seawater injection on the chemical and physical state of the corium debris formed in the severe accident at Fukushima Daiichi Nuclear Power Plants, the high temperature reaction between sea salt deposit and (U,Zr)O2 simulated corium debris (sim-debris) was examined in the temperature range from 1088 to 1668 K. A dense layer of calcium and sodium uranate formed on the surface of a sim-debris pellet at 1275 K under airflow, with the thickness of over 50 μm. When the oxygen partial pressure is low, calcium is likely to dissolve into the cubic sim-debris phase to form solid solution (Ca,U,Zr)O2+x. The diffusion depth was 5-6 μm from the surface, subjected to 1275 K for 12 h. The crystalline MgO remains affixed on the surface as the main residue of salt components. A part of it can also dissolve into the sim-debris.

  18. Conformation of the umifenovir cation in the molecular and crystal structures of four carboxylic acid salts

    NASA Astrophysics Data System (ADS)

    Orola, Liana; Sarcevica, Inese; Kons, Artis; Actins, Andris; Veidis, Mikelis V.

    2014-01-01

    The umifenovir salts of maleic, salicylic, glutaric, and gentisic acid as well as the chloroform solvate of the salicylate were prepared. Single crystals of the five compounds were obtained and their molecular and crystal structures determined by X-ray diffraction. In each structure the conformation of phenyl ring with respect to the indole group of the umifenovir moiety is different. The water solubility and melting points of the studied umifenovir salts have been determined.

  19. 76 FR 34044 - Citric Acid and Certain Citrate Salts From Canada: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-06-10

    ... Citrate Salts From Canada: Preliminary Results of Antidumping Duty Administrative Review, 76 FR 5782... Duties, 68 FR 23954 (May 6, 2003) (Assessment Policy Notice). This clarification will apply to entries of... Republic of China: Antidumping Duty Orders, 74 FR 25703 (May 29, 2009). These deposit requirements...

  20. 40 CFR 721.10202 - Benzoic acid, 4-chloro-2- [(substituted)azo]-, strontium salt (1:1) (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Benzoic acid, 4-chloro-2- -, strontium... New Uses for Specific Chemical Substances § 721.10202 Benzoic acid, 4-chloro-2- -, strontium salt (1:1... identified generically as benzoic acid, 4-chloro-2- -, strontium salt (1:1) (PMN P-08-701) is subject...

  1. 40 CFR 721.10202 - Benzoic acid, 4-chloro-2- [(substituted)azo]-, strontium salt (1:1) (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Benzoic acid, 4-chloro-2- -, strontium... New Uses for Specific Chemical Substances § 721.10202 Benzoic acid, 4-chloro-2- -, strontium salt (1:1... identified generically as benzoic acid, 4-chloro-2- -, strontium salt (1:1) (PMN P-08-701) is subject...

  2. 40 CFR 721.10202 - Benzoic acid, 4-chloro-2- [(substituted)azo]-, strontium salt (1:1) (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Benzoic acid, 4-chloro-2- -, strontium... New Uses for Specific Chemical Substances § 721.10202 Benzoic acid, 4-chloro-2- -, strontium salt (1:1... identified generically as benzoic acid, 4-chloro-2- -, strontium salt (1:1) (PMN P-08-701) is subject...

  3. 40 CFR 721.10202 - Benzoic acid, 4-chloro-2- [(substituted)azo]-, strontium salt (1:1) (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Benzoic acid, 4-chloro-2- -, strontium... New Uses for Specific Chemical Substances § 721.10202 Benzoic acid, 4-chloro-2- -, strontium salt (1:1... identified generically as benzoic acid, 4-chloro-2- -, strontium salt (1:1) (PMN P-08-701) is subject...

  4. 77 FR 1455 - Citric Acid and Certain Citrate Salts From the People's Republic of China: Extension of Time...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-01-10

    ..., 76 FR 37781, 37785 (June 28, 2011). This review covers the period May 1, 2010, through April 30, 2011... International Trade Administration Citric Acid and Certain Citrate Salts From the People's Republic of China... acid and certain citrate salts (``citric acid'') from the People's Republic of China (``PRC'')....

  5. 77 FR 9891 - Citric Acid and Certain Citrate Salts from the People's Republic of China: Amended Final Results...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-02-21

    ... Republic of China: Final Results of the First Administrative Review of the Antidumping Duty Order, 76 FR... International Trade Administration Citric Acid and Certain Citrate Salts from the People's Republic of China... antidumping duty order on citric acid and certain citrate salts (``citric acid'') from the People's...

  6. Synthesis and biological activity of arylspiroborate salts derived from caffeic Acid phenethyl ester.

    PubMed

    Hébert, Martin J G; Flewelling, Andrew J; Clark, Trevor N; Levesque, Natalie A; Jean-François, Jacques; Surette, Marc E; Gray, Christopher A; Vogels, Christopher M; Touaibia, Mohamed; Westcott, Stephen A

    2015-01-01

    Two novel boron compounds containing caffeic acid phenethyl ester (CAPE) derivatives have been prepared and characterized fully. These new compounds and CAPE have been investigated for potential antioxidant and antimicrobial properties and their ability to inhibit 5-lipoxygenase and whether chelation to boron improves their biological activity. Sodium salt 4 was generally more active than ammonium salt 5 in the biological assays and surpassed the radical scavenging ability of CAPE. Compounds 4 and 5 were more active than CAPE and Zileuton in human polymorphonuclear leukocytes. These results clearly show the effectiveness of the synthesized salts as transporter of CAPE. PMID:25834744

  7. Synthesis and Biological Activity of Arylspiroborate Salts Derived from Caffeic Acid Phenethyl Ester

    PubMed Central

    Hébert, Martin J. G.; Flewelling, Andrew J.; Clark, Trevor N.; Jean-François, Jacques; Surette, Marc E.; Gray, Christopher A.; Vogels, Christopher M.; Touaibia, Mohamed; Westcott, Stephen A.

    2015-01-01

    Two novel boron compounds containing caffeic acid phenethyl ester (CAPE) derivatives have been prepared and characterized fully. These new compounds and CAPE have been investigated for potential antioxidant and antimicrobial properties and their ability to inhibit 5-lipoxygenase and whether chelation to boron improves their biological activity. Sodium salt 4 was generally more active than ammonium salt 5 in the biological assays and surpassed the radical scavenging ability of CAPE. Compounds 4 and 5 were more active than CAPE and Zileuton in human polymorphonuclear leukocytes. These results clearly show the effectiveness of the synthesized salts as transporter of CAPE. PMID:25834744

  8. Emissions involved in acidic deposition processes: Methodology and results

    SciTech Connect

    Placet, M.

    1990-01-01

    Data on the emissions involved in atmospheric acid-base chemistry are crucial to the assessment of acidic deposition and its effects. Sulfur dioxide (SO{sub 2}), nitrogen oxides (NO{sub x}), and volatile organic compounds (VOCs) are the primary chemical compounds involved in acidic deposition processes. In addition, other emission species -- e.g., ammonia, alkaline dust particles, hydrogen chloride, and hydrogen fluoride -- are involved in atmospheric acid-base chemistry, either by contributing acidic constituents or by neutralizing acidic species. Several emissions data bases have been developed under the auspices of the National Acid Precipitation Program (NAPAP). In addition to those developed by NAPAP, emissions data bases and emissions trends estimates also have been developed by organizations such as the Electric Power Research Institute (EPRI) and the U.S. Environmental Protection Agency (EPA). This paper briefly describes and compares the methods used in developing these emissions data bases and presents an overview of their emissions estimates. A more detailed discussion of these topics can be found in the State-of-Science Report on emissions recently released by NAPAP and in the references cited in that report. 14 refs., 4 figs., 1 tab.

  9. Electrophoretic deposition of tannic acid-polypyrrolidone films and composites.

    PubMed

    Luo, Dan; Zhang, Tianshi; Zhitomirsky, Igor

    2016-05-01

    Thin films of polyvinylpyrrolidone (PVP)-tannic acid (TA) complexes were prepared by a conceptually new strategy, based on electrophoretic deposition (EPD). Proof of concept investigations involved the analysis of the deposition yield, FTIR and UV-vis spectroscopy of the deposited material, and electron microscopy studies. The analysis of the deposition mechanism indicated that the limitations of the EPD in the deposition of small phenolic molecules, such as TA, and electrically neutral polymers, similar to PVP, containing hydrogen-accepting carbonyl groups, can be avoided. The remarkable adsorption properties of TA and film forming properties of the PVP-TA complexes allowed for the EPD of materials of different types, such as huntite mineral platelets and hydrotalcite clay particles, TiO2 and MnO2 oxide nanoparticles, multiwalled carbon nanotubes, TiN and Pd nanoparticles. Moreover, PVP-TA complexes were used for the co-deposition of different materials and formation of composite films. In another approach, TA was used as a capping agent for the hydrothermal synthesis of ZnO nanorods, which were then deposited by EPD using PVP-TA complexes. The fundamental adsorption and interaction mechanisms of TA involved chelation of metal atoms on particle surfaces with galloyl groups, π-π interactions and hydrogen bonding. The films prepared by EPD can be used for various applications, utilizing functional properties of TA, PVP, inorganic and organic materials of different types and their composites. PMID:26878711

  10. A Martian analog in Kansas: Comparing Martian strata with Permian acid saline lake deposits

    NASA Astrophysics Data System (ADS)

    Benison, Kathleen C.

    2006-05-01

    An important result of the Mars Exploration Rover's (MER) mission has been the images of sedimentary structures and diagenetic features in the Burns Formation at Meridiani Planum. Bedding, cross-bedding, ripple marks, mud cracks, displacive evaporite crystal molds, and hematite concretions are contained in these Martian strata. Together, these features are evidence of past saline groundwater and ephemeral shallow surface waters on Mars. Geochemical analyses of these Martian outcrops have established the presence of sulfates, iron oxides, and jarosite, which strongly suggests that these waters were also acidic. The same assemblage of sedimentary structures and diagenetic features is found in the salt-bearing terrestrial red sandstones and shales of the middle Permian (ca. 270 Ma) Nippewalla Group of Kansas, which were deposited in and around acid saline ephemeral lakes. These striking sedimentological and mineralogical similarities make these Permian red beds and evaporites the best-known terrestrial analog for the Martian sedimentary rocks at Meridiani Planum.

  11. Process for the preparation of 3,4-dihydroxybutanoic acid and salts thereof

    DOEpatents

    Hollingsworth, Rawle I.

    1994-01-01

    A process for the preparation of 3,4-dihydroxybutanoic acid (1) and salts thereof from a glucose source containing 1,4-linked glucose as a substituent is described. The process uses an alkali metal hdyroxide and hydrogen peroxide to convert the glucose source to (1). The compound (1) is useful as a chemical intermediate to naturally occurring fatty acids and is used to prepare 3,4-dihydroxybutanoic acid-gamma-lactone (2) and furanone (3), particularly stereoisomers of these compounds.

  12. Process For The Preparation Of 3,4-Dihyd Roxybutanoic Acid And Salts Thereof

    DOEpatents

    Hollingsworth, Rawle I.

    1994-06-07

    A process for the preparation of 3,4-dihydroxybutanoic acid (1) and salts thereof from a glucose source containing 1,4-linked glucose as a substituent is described. The process uses an alkali metal hdyroxide and hydrogen peroxide to convert the glucose source to (1). The compound (1) is useful as a chemical intermediate to naturally occurring fatty acids and is used to prepare 3,4-dihydroxybutanoic acid-gamma-lactone (2) and furanone (3), particularly stereoisomers of these compounds.

  13. MOUNTAIN ACID DEPOSITION PROGRAM (MADPRO): CLOUD DEPOSITION TO THE APPALACHIAN MOUNTAINS, 1994 THROUGH 1999

    EPA Science Inventory

    The mountain Acid Deposition Program (MADPro) was initiated in 1993 as part of the research necessary to support the objectives of the Clean Air Status and Trends Network (CASTNet), which was created to address the requirements of the Clean Air Act Amendments (CAAA). The two ma...

  14. Second-harmonic generation in mixed stilbazium salt/arachidic acid Langmuir-Blodgett films

    NASA Astrophysics Data System (ADS)

    Liu, Liying; Zheng, Jiabiao; Wang, Wencheng; Zhang, Zhiming; Tao, Fenggang; Xu, Linxiao; Hu, Jiacong

    1992-10-01

    A stilbazium salt was synthesized and its second-order molecular polarizability was deduced to be 1.2×10 -27 esu. Measurements of second-harmonic generation and small-angle X-ray diffraction on Langmuir-Blodgett films of the stilbazium salt/arachide acid mixtures showed that the mixed compounds with molar ratios of 1:2 and 1:5 could form multilayers with large second- order optical nonlinearity. Second harmonic generation study on the alternate multilayers of stilbazium salt/arachide acid and arachidic acid showed that the second-harmonic signals were increasing monotonously up to 80 bilayers, but the increment was lower than the value predicted theoretically by the quadratic law. Possible reasons are discussed.

  15. Critical supersaturations for aerosol particles of succinic acid and its salts

    NASA Astrophysics Data System (ADS)

    Svenningsson, B.; Bilde, M.; Rosenørn, T.; Mønster, J.

    2003-04-01

    Dicarboxylic acids, like succinic acid, have been identified as important water soluble organic compounds in the atmosphere. Salts of carboxylic acids can be formed in the atmosphere in reactions between the acid and an inorganic salt. In this work we have studied the cloud droplet nucleating ability for succinic acid and some of its salts: disodium succinate, diammonium succinate and calcium succinate. A monodisperse aerosol was generated by atomizing a water solution of the compound of interest, drying the particles in diffusion driers and selecting a narrow size range using a differential mobility analyzer. The aerosol was then analyzed using a static thermal gradient cloud condensation nucleus spectrometer (CCNC-100B from the University of Wyoming). A CPC was used to count the number of particles as a reference. For a fixed particle diameter, the supersaturation was scanned to find a steep increase in the fraction of particles that were activated to cloud droplets. This critical supersaturation is compared with theoretical calculations using Köhler theory. Experimental critical supersaturations for succinic acid agree with Köhler theory with a van't Hoff factor of 1, i.e. it activates as if it does not dissociate. For the sodium salt, a van't Hoff factor of 2 fits laboratory data and theoretical calculations.

  16. Role of acid rain in atmospheric deposition. Final report

    SciTech Connect

    Winchester, J.W.

    1990-12-31

    A study was conducted to assess the potential importance of atmospheric nitrate deposition for a north Florida estuary. A comparison, based on statistical analysis of fluxes of ten dissolved constituents of rain water and river water, has been carried out for the watershed of the Apalachicola River, utilizing weekly rain water chemical data from the National Acid Deposition Program (NADP) for five sites within the watershed area, monitored from 1978-84 until late 1989, and less frequent river water chemical data from the U.S. Geological Survey for one site at Chattahoochee, Florida, monitored from 1965 until late 1989. Similar statistical analysis was performed on monitoring data for the Sopchoppy and Ochlockonee Rivers of north Florida. Atmospheric deposition to the watershed appears to be sufficient to account for essentially all the dissolved nitrate and ammonium and total organic nitrogen flow in the three rivers. However, after deposition most of the nitrate may be transformed to other chemical forms during the flow of the rivers toward their estuaries. In an additional statistical analysis of rain water monitoring data from the eight state southeastern USA region, it was found that both meteorological conditions and transport from pollution sources appear to control deposition fluxes of nitrate and sulfate acid air pollutants.

  17. Estimates of cloud water deposition at Mountain Acid Deposition Program sites in the Appalachian Mountains.

    PubMed

    Baumgardner, Ralph E; Isil, Selma S; Lavery, Thomas F; Rogers, Christopher M; Mohnen, Volker A

    2003-03-01

    Cloud water deposition was estimated at three high-elevation sites in the Appalachian Mountains of the eastern United States (Whiteface Mountain, NY; Whitetop Mountain, VA; and Clingman's Dome, TN) from 1994 through 1999 as part of the Mountain Acid Deposition Program (MADPro). This paper provides a summary of cloud water chemistry, cloud liquid water content, cloud frequency, estimates of cloud water deposition of sulfur and nitrogen species, and estimates of total deposition of sulfur and nitrogen at these sites. Other cloud studies in the Appalachians and their comparison to MADPro are also summarized. Whiteface Mountain exhibited the lowest mean and median concentrations of sulfur and nitrogen ions in cloud water, while Clingman's Dome exhibited the highest mean and median concentrations. This geographic gradient is partly an effect of the different meteorological conditions experienced at northern versus southern sites in addition to the difference in pollution content of air masses reaching the sites. All sites measured seasonal cloud water deposition rates of SO4(2-) greater than 50 kg/ha and NO3(-) rates of greater than 25 kg/ha. These high-elevation sites experienced additional deposition loading of SO4(2-) and NO3(-) on the order of 6-20 times greater compared with lower elevation Clean Air Status and Trends Network (CASTNet) sites. Approximately 80-90% of this extra loading is from cloud deposition. PMID:12661689

  18. [Inhibitory effects of organic acids and salts on selected micromycetes].

    PubMed

    Láníková, A; Toulová, M

    1992-12-01

    Inhibitory effects of two fungistatic preparations (A and B) and of propionic acid were tested in a complete feed mixture for broiler chickens (starter mixture). The water content of this mixture was 25.4%, environmental temperature was 24 degrees C and relative air humidity 90%. Propionic acid, which has a high fungistatic effect, served as a standard. The composition of the preparation A was as follows: propionic acid, acetic acid, sorbic acid, citric acid and calcium propionate. The preparation B contained: sorbic acid, citric acid and calcium propionate. Examinations were performed in a naturally contaminated and subsequently sterilized (25 kGy) feed mixture; it was then infected with Aspergillus fumigatus, A. niger, A. parasiticus and Penicillium purpurogenum from the Collection of Animal Pathogenic Microorganisms, Brno. A. flavus, A. fumigatus, A. glaucus, Penicillium sp., Absidia corymbifera, Mucor sp., Rhizomucor pusillus were detected in the naturally contaminated feed mixture. The mycoflora which was found in the native substrate was resistant to both tested fungistatic preparations; and this resulted in mycelium growth from 7th day of incubation. The efficiency of the preparations A,B and of propionic acid in the feed mixture was identical at concentrations of 4 mg/kg, 7 mg/kg and 3 mg/kg, respectively, and their inhibitory effects were lowest at these concentrations (Fig. 2). A high water content in the nutrient substrate resulted in the rapid growth of fungi of the Mucorales species. The relative humidity of the environment (90%) and water content of tested samples affected markedly micromycetes growth in this experiment.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:1297244

  19. Deposition of ammonium and nitrate in the roots of maize seedlings supplied with different nitrogen salts

    PubMed Central

    Bloom, Arnold J.; Randall, Lesley; Taylor, Alison R.; Silk, Wendy K.

    2012-01-01

    This study measured total osmolarity and concentrations of NH4+, NO3–, K+, soluble carbohydrates, and organic acids in maize seminal roots as a function of distance from the apex, and NH4+ and NO3– in xylem sap for plants receiving NH4+ or NO3– as a sole N-source, NH4+ plus NO3–, or no nitrogen at all. The disparity between net deposition rates and net exogenous influx of NH4+ indicated that growing cells imported NH4+ from more mature tissue, whereas more mature root tissues assimilated or translocated a portion of the NH4+ absorbed. Net root NO3– influx under Ca(NO3)2 nutrition was adequate to account for pools found in the growth zone and provided twice as much as was deposited locally throughout the non-growing tissue. In contrast, net root NO3– influx under NH4NO3 was less than the local deposition rate in the growth zone, indicating that additional NO3– was imported or metabolically produced. The profile of NO3– deposition rate in the growth zone, however, was similar for the plants receiving Ca(NO3)2 or NH4NO3. These results suggest that NO3– may serve a major role as an osmoticant for supporting root elongation in the basal part of the growth zone and maintaining root function in the young mature tissues. PMID:22213811

  20. Drilling the Messinian Salinity Crisis as a Model Analogue for Dolomite Deposition at the End of Massive Salt Deposition Events

    NASA Astrophysics Data System (ADS)

    McKenzie, Judith A.; Aloisi, Giovanni; Anjos, Sylvia; Latgé, Ricardo; Matsuda, Nilo; Bontognali, Tomaso; Vasconcelos, Crisogono

    2015-04-01

    Sedimentologic and stratigraphic studies of the Lower Cretaceous sequence, deposited in the economically important Campos Basin, southeast Brazil, document the occurrence of ~20-m-thick dolomite intervals overlying the "massive salt" megasequences of the Lagoa Feia Formation. This stratigaphic succession marks the Aptian/Albian transition from extreme evaporitic conditions of the Lagoa Feia Formation to shallow marine conditions of the Macaé Formation, related to the early opening of the South Atlantic. The facies change from evaporites to dolomite is interpreted as a product of dolomitization resulting from the refuxing of hypersaline fluids from shallow embayments with intense evaporation (Latgé, 2001). Although the reflux model provides a mechanism to produce fluids with geochemical composition favorable for dolomite precipitation, it cannot account for all of the factors required to promote dolomite precipitation. In this study, we propose a different model to explain the post-evaporite deposition of massive dolomite based on the study of sequences deposited at the end Messinian Salinity Crisis, which were recovered from the deep basins of the Mediterranean Sea during DSDP/ODP drilling campaigns. At most of these deep-water sites, the cored interval contained unusual dolomite deposits overlying the uppermost evaporite sections. For example, the upper Messinian sedimentary sequence at DSDP Site 374 comprises non-fossiliferous dolomitic mudstone overlying dolomitic mudstone/gypsum cycles, which in turn overlie anhydrite and halite (Hsü, Montadert et al., 1978). We postulate that the end Messinian dolomite is a product of microbial activity under extreme hypersaline conditions. In the last 20 years, research into the factors controlling dolomite precipitation under Earth surface conditions has led to the development of new models involving the metabolism of microorganisms and associated biofilms to overcome the kinetic inhibitions associated with primary

  1. Simulated seasonal variations in wet acid depositions over East Asia.

    PubMed

    Ge, Cui; Zhang, Meigen; Zhu, Lingyun; Han, Xiao; Wang, Jun

    2011-11-01

    The air quality modeling system Regional Atmospheric Modeling System-Community Multi-scale Air Quality (RAMS-CMAQ) was applied to analyze temporospatial variations in wet acid deposition over East Asia in 2005, and model results obtained on a monthly basis were evaluated against extensive observations, including precipitation amounts at 704 stations and SO4(2-), NO3-, and NH4+ concentrations in the atmosphere and rainwater at 18 EANET (the Acid Deposition Monitoring Network in East Asia) stations. The comparison shows that the modeling system can reasonably reproduce seasonal precipitation patterns, especially the extensive area of dry conditions in northeast China and north China and the major precipitation zones. For ambient concentrations and wet depositions, the simulated results are in reasonable agreement (within a factor of 2) with observations in most cases, and the major observed features are mostly well reproduced. The analysis of modeled wet deposition distributions indicates that East Asia experiences noticeable variations in its wet deposition patterns throughout the year. In winter, southern China and the coastal areas of the Japan Sea report higher S04(2-) and NO3- wet depositions. In spring, elevated SO4(2-) and NO3-wet depositions are found in northeastern China, southern China, and around the Yangtze River. In summer, a remarkable rise in precipitation in northeastern China, the valleys of the Huaihe and Yangtze rivers, Korea, and Japan leads to a noticeable increase in SO4(2-) and NO3- wet depositions, whereas in autumn, higher SO4(2-) and NO3-wet depositions are found around Sichuan Province. Meanwhile, due to the high emission of SO2, high wet depositions of SO4(2-) are found throughout the entire year in the area surrounding Sichuan Province. There is a tendency toward decreasing NO3- concentrations in rainwater from China through Korea to Japan in both observed and simulated results, which is a consequence of the influence of the continental

  2. Thermodynamics of binding water and solute to powdered long-chain salts of fatty acids.

    PubMed

    Mahapatra, P K; Chattoraj, D K

    1994-10-01

    Hydration of powdered fatty acids and their salts has been studied both in presence and absence of neutral salts, sucrose and urea using the isopiestic vapour pressure technique. Moles of water vapour adsorbed per mole or kg of soaps like sodium palmitate, sodium stearate, sodium myristate and sodium laurate have been measured in presence and absence of salts and compared with that of detergents (SDS, CTAB, DTAB and MTAB). For each case of positive excess adsorption of water vapour and negative excess adsorption of inorganic salts, urea and sucrose to different soaps, the standard free energy change (delta G degrees) per kg of substrate in bringing the bulk mole fraction from zero to unity have been calculated using an appropriate thermodynamic equation and the values so obtained have been compared critically. PMID:7851944

  3. ACIDIC DEPOSITION IN THE NORTHEASTERN U.S.: SOURCES AND INPUTS, ECOSYSTEM EFFECTS, AND MANAGEMENT STRATEGIES

    EPA Science Inventory

    Acidic deposition results from the emissions of air pollutants. Effects of acidic deposition in the northeastern US include the acidification of soil and water, causing stresses to terrestrial and aquatic biota.

  4. Silica precipitation in acidic solutions: mechanism, pH effect, and salt effect.

    PubMed

    Gorrepati, Elizabeth A; Wongthahan, Pattanapong; Raha, Sasanka; Fogler, H Scott

    2010-07-01

    This study is the first to show that silica precipitation under very acidic conditions ([HCl] = 2-8 M) proceeds through two distinct steps. First, the monomeric form of silica is quickly depleted from solution as it polymerizes to form primary particles approximately 5 nm in diameter. Second, the primary particles formed then flocculate. A modified Smoluchowski equation that incorporates a geometric population balance accurately describes the exponential growth of silica flocs. Variation of the HCl concentration between 2 and 8 M further showed that polymerization to form primary particles and subsequent particle flocculation become exponentially faster with increasing acid concentration. The effect of salt was also studied by adding 1 M chloride salts to the solutions; it was found that salts accelerated both particle formation and growth rates in the order: AlCl(3) > CaCl(2) > MgCl(2) > NaCl > CsCl > no salt. It was also found that ionic strength, over cation identity, determines silica polymerization and particle flocculation rates. This research reveals that precipitation of silica products from acid dissolution of minerals can be studied apart from the mineral dissolution process. Thus, silica product precipitation from mineral acidization follows a two-step process--formation of 5 nm primary particles followed by particle flocculation--which becomes exponentially faster with increasing HCl concentration and with salts accelerating the process in the above order. This result has implications for any study of acid dissolution of aluminosilicate or silicate material. In particular, the findings are applicable to the process of acidizing oil-containing rock formations, a common practice of the petroleum industry where silica dissolution products encounter a low-pH, salty environment within the oil well. PMID:20536253

  5. Life at high salt concentrations, intracellular KCl concentrations, and acidic proteomes

    PubMed Central

    Oren, Aharon

    2013-01-01

    Extremely halophilic microorganisms that accumulate KCl for osmotic balance (the Halobacteriaceae, Salinibacter) have a large excess of acidic amino acids in their proteins. This minireview explores the occurrence of acidic proteomes in halophiles of different physiology and phylogenetic affiliation. For fermentative bacteria of the order Halanaerobiales, known to accumulate KCl, an acidic proteome was predicted. However, this is not confirmed by genome analysis. The reported excess of acidic amino acids is due to a high content of Gln and Asn, which yield Glu and Asp upon acid hydrolysis. The closely related Halorhodospira halophila and Halorhodospira halochloris use different strategies to cope with high salt. The first has an acidic proteome and accumulates high KCl concentrations at high salt concentrations; the second does not accumulate KCl and lacks an acidic proteome. Acidic proteomes can be predicted from the genomes of some moderately halophilic aerobes that accumulate organic osmotic solutes (Halomonas elongata, Chromohalobacter salexigens) and some marine bacteria. Based on the information on cultured species it is possible to understand the pI profiles predicted from metagenomic data from hypersaline environments. PMID:24204364

  6. 40 CFR 721.10098 - Disubstituted benzoic acid, alkali metal salt (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... metal salt (generic). 721.10098 Section 721.10098 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10098 Disubstituted benzoic acid, alkali metal...

  7. 21 CFR 173.45 - Polymaleic acid and its sodium salt.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polymaleic acid and its sodium salt. 173.45 Section 173.45 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) SECONDARY DIRECT FOOD ADDITIVES PERMITTED IN FOOD FOR HUMAN CONSUMPTION Polymer Substances and...

  8. 21 CFR 173.45 - Polymaleic acid and its sodium salt.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polymaleic acid and its sodium salt. 173.45 Section 173.45 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) SECONDARY DIRECT FOOD ADDITIVES PERMITTED IN FOOD FOR HUMAN CONSUMPTION Polymer Substances and...

  9. 21 CFR 173.45 - Polymaleic acid and its sodium salt.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polymaleic acid and its sodium salt. 173.45 Section 173.45 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) SECONDARY DIRECT FOOD ADDITIVES PERMITTED IN FOOD FOR HUMAN CONSUMPTION Polymer Substances and...

  10. Esterification and transesterification of greases to fatty acid methyl esters with highly active diphanylammonium salts

    Technology Transfer Automated Retrieval System (TEKTRAN)

    We have conducted an investigation designed to identify alternate catalysts for the production of fatty acid methyl esters (FAME) to be used as biodiesel. Diphenylammonium sulfate (DPAS) and diphenylammonium chloride (DPA-HCl) salts were found to be highly active homogeneous catalysts for the simu...

  11. Esterification and Transesterification of greases to fatty acid methyl esters with highly active diphenylamine salts

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Diphenylamine sulfate (DPAS) and diphenylamine hydrochloride (DPACl) salts were found to be highly active catalysts for esterification and transesterification of inexpensive greases to fatty acid methyl esters (FAME). In the presence of catalytic amounts of DPAS or DPACl and excess methanol, the fr...

  12. Triarylsulfonium hexafluorophosphate salts as photoactivated acidic catalysts for ring-opening polymerisation.

    PubMed

    Barker, Ian A; Dove, Andrew P

    2013-02-11

    Triarylsulfonium hexafluorophosphate salts were shown to be effective catalysts for the ring-opening polymerisation of various cyclic monomers under UV irradiation. A dual basic/acidic catalytic system demonstrated the potential for UV-triggered formation of poly(δ-valerolactone)-b-poly(L-lactide)-b-poly(δ-valerolactone) in a 'one-pot' reaction. PMID:23283246

  13. Salt and mesophase formation in aqueous suspensions of lauric acid.

    PubMed

    Smith, S W; Anderson, B D

    1993-10-01

    The solubility and solution behavior of lauric acid (LA) and its 1:1 acid soap (potassium hydrogen dilaurate) were investigated at 32 degrees C over a pH range of 2.5-8.5 and at varying KCl concentrations to examine the self-association of this long-chain carboxylic acid under these conditions. LA's solubility in water exhibited the classical pH dependence of a monocarboxylic acid with no evidence of self-association. In 0.1 M KCl between pH 6.3 and pH 7.3, filtered samples were turbid, suggesting the presence of high molecular weight aggregates (mesophase), which could be removed by ultrafiltration. The apparent LA solubility vs pH profile in ultrafiltered samples was consistent with a solid phase consisting of either the free acid (pH < 6.5) or potassium hydrogen dilaurate (pH > 6.5), again with no evidence of self-association to form low molecular weight species (dimers, etc.). Quasi-elastic light scattering (QLS) studies and mannitol trapping experiments indicated that vesicles were present in samples containing mesophase. The mesophase composition was characterized and a mass-action law for mesophase formation was developed to describe the apparent LA solubility versus pH in the mesophase region in terms of three parameters. The index of cooperativity, theta, indicated that the mesophase consists of approximately 25 molecules of LA with an acid:anion ratio, rho, of 1.7. The standard free energy of mesophase formation per mole of monomer was determined to be -6.3 kcal/mol. The aggregate size determined thermodynamically is several orders of magnitude less than that of the mesophase particle size determined by QLS measurements, suggesting that the LA monomer concentration in equilibrium with mesophase may be governed by a small unit domain of the vesicle. These observations may have a bearing on the thermodynamics of self-assembly of lipid bilayer membranes. PMID:8272419

  14. Effect alteration of methamphetamine by amino acids or their salts on ambulatory activity in mice.

    PubMed

    Kuribara, H; Tadokoro, S

    1983-02-01

    Effect alterations of methamphetamine by pretreatment of amino acids or their salts on ambulatory activity in mice were investigated to confirm a fact that certain amino acids, particularly monosodium L-glutamate, are added to methamphetamine by the street users, and that the amino acids augment the effect of methamphetamine. The ambulatory activity of mouse was measured by a tilting-type round activity cage of 25 cm in diameter. The amino acids or their salts tested were monosodium L-glutamate, monosodium L-aspartate, gamma-amino-butyric acid, L-alanine, L-lysine hydrochloride and L-arginine hydrochloride. A single administration of each chemical at doses of 1 and 2 g/kg i.p. did not induce a marked change in the ambulatory activity in mice. Methamphetamine 2 mg/kg s.c. induced an increase in the ambulatory activity with a peak at 40 min after the administration, and the increased ambulatory activity persisted for 3 hr. The ambulation-increasing effect of methamphetamine was augmented by the pretreatment of monosodium L-glutamate and monosodium L-aspartate at 30 min before the methamphetamine administration, while attenuated by the pretreatment of L-lysine hydrochloride and L-arginine hydrochloride in a dose-dependent manner. Gamma-aminobutyric acid and L-alanine did not affect the effect of methamphetamine. Similar augmentation and attenuation in the ambulation-increasing effect of methamphetamine were induced by the pretreatment of sodium bicarbonate 0.9 g/kg i.p. (urinary alkalizer) and ammonium chloride 0.07 g/kg i.p. (urinary acidifier), respectively. The urinary pH level was elevated by the administration of monosodium L-glutamate, monosodium L-aspartate and sodium bicarbonate, and decreased by L-lysine hydrochloride, L-arginine hydrochloride and ammonium chloride. Gamma-aminobutyric acid and L-alanine did not elicit a marked change in the urinary pH level. The present experiment confirms the fact in human that monosodium L-glutamate augments the effect of

  15. Regulation of ion homeostasis by aminolevulinic acid in salt-stressed wheat seedlings

    NASA Astrophysics Data System (ADS)

    Türk, Hülya; Genişel, Mucip; Erdal, Serkan

    2016-04-01

    Salinity is regarded as a worldwide agricultural threat, as it seriously limits plant development and productivity. Salt stress reduces water uptake in plants by disrupting the osmotic balance of soil solution. In addition, it creates a damaged metabolic process by causing ion imbalance in cells. In this study, we aim to examine the negative effects of 5-aminolevulinic acid (ALA) (20 mg/l) on the ion balance in wheat seedling leaves exposed to salt stress (150 mM). Sodium is known to be highly toxic for plant cells at high concentrations, and is significantly increased by salt stress. However, it can be reduced by combined application of ALA and salt, compared to salt application alone. On the other hand, while the K+/Na+ ratio was reduced by salt stress, ALA application changed this ratio in favor of K+. Manganese, iron, and copper were also able to reduce stress. However, ALA pre-treatment resulted in mineral level increments. Conversely, the stress-induced rise in magnesium, potassium, calcium, phosphorus, zinc, and molybdenum were further improved by ALA application. These data clearly show that ALA has an important regulatory effect of ion balance in wheat leaves.

  16. Aggregation of 12-Hydroxystearic Acid and Its Lithium Salt in Hexane: Molecular Dynamics Simulations.

    PubMed

    Gordon, Ryan; Stober, Spencer T; Abrams, Cameron F

    2016-07-28

    12-Hydroxystearic acid (12HSA) is a well-known organogelator, and its metal salts and derivatives find roles in many important applications. The structures of aggregates of 12-hydroxysteric acid and its salts depend sensitively on cation type, but a fundamental understanding of this phenomenon is lacking. In this study, molecular dynamics simulations were conducted on the microsecond long time scales for (1) 12HSA and (2) its lithium salt, each at 12.5 wt % in explicit hexane solvent. Self-assembly was accelerated by using a modified potential to prohibit alkane chain dihedral gauche states (all-trans-12HSA) and then verified by continuation using standard force-field parameters. In three independent simulation, acceleration using "gauche-less" potentials resulted in self-assembled pseudocrystalline aggregates through formation of polarized five- and six-membered rings between inter-12-hydroxyl groups and head-to-head carboxylic acid dimerization. When subjected to the unmodified dihedral potential, two of the three structures remained stable after 1 μs of MD. Stable structures exhibited a "ring-of-rings" motif, composed of two six-membered acetic acid-dimerized ring bundles with six satellite rings, while the unstable structure did not. In strong contrast, the lithium salt produced a network of fibrils that spanned the volume of the sample. When lithium ions were substituted for carboxylic acid protons in the stable acid structures, they remained intact but lost their chiral nature. Both the acid and lithium structures displayed scattering peaks that agreed with experiment. Taken together, our results suggest that this ring-of-rings structure could be a primary feature of the self-assembly of 12HSA in organic solvents. PMID:27387154

  17. Effects of some components of acid-mine drainage and acid deposition on the spermatozoa of longear sunfish, Lepomis megalotis

    SciTech Connect

    Pearson, B.J.

    1983-01-01

    The effects of low pH and the metals aluminum, zinc, and cadmium, components of acid-mine effluents and acid deposition, on spermatozoa of longear sunfish, Lepomis megalotis, were investigated. Sperm were exposed to solutions of 400 ppm aluminum chloride, 50 ppm zinc chloride, 2 ppm cadmium chloride, separately and in combination, at pH values of 6.9, 4.8, and 3.8. Sperm were additionally exposed to test solutions in which the metal salt concentration was reduced by one-half and observed for changes in motility and in the ability to exclude stain. All test solutions at a low pH were deleterious, the greatest damage occurring in solutions of a combination of all 3 metal chlorides and of aluminum chloride separately. Motility tests showed that both full and reduced metal concentrations had significant effects on motility. Staining tests were supportive of motility test results and indicated that in most cases shorter exposure times did not significantly improve survival rates. It was generally found that a decrease in pH increased the effects of each metal separately and when combined. Aluminum, zinc, and cadmium chlorides appeared to act antagonistically when tested in combination. It was concluded that the components of acid waters which were tested have deleterious effects on longer spermatozoa, reducing their viability and thereby reducing reproductive success of the species.

  18. Bile salt recognition by human liver fatty acid binding protein.

    PubMed

    Favretto, Filippo; Santambrogio, Carlo; D'Onofrio, Mariapina; Molinari, Henriette; Grandori, Rita; Assfalg, Michael

    2015-04-01

    Fatty acid binding proteins (FABPs) act as intracellular carriers of lipid molecules, and play a role in global metabolism regulation. Liver FABP (L-FABP) is prominent among FABPs for its wide ligand repertoire, which includes long-chain fatty acids as well as bile acids (BAs). In this work, we performed a detailed molecular- and atomic-level analysis of the interactions established by human L-FABP with nine BAs to understand the binding specificity for this important class of cholesterol-derived metabolites. Protein-ligand complex formation was monitored using heteronuclear NMR, steady-state fluorescence spectroscopy, and mass spectrometry. BAs were found to interact with L-FABP with dissociation constants in the narrow range of 0.6-7 μm; however, the diverse substitution patterns of the sterol nucleus and the presence of side-chain conjugation resulted in complexes endowed with various degrees of conformational heterogeneity. Trihydroxylated BAs formed monomeric complexes in which single ligand molecules occupied similar internal binding sites, based on chemical-shift perturbation data. Analysis of NMR line shapes upon progressive addition of taurocholate indicated that the binding mechanism departed from a simple binary association equilibrium, and instead involved intermediates along the binding path. The co-linear chemical shift behavior observed for L-FABP complexes with cholate derivatives added insight into conformational dynamics in the presence of ligands. The observed spectroscopic features of L-FABP/BA complexes, discussed in relation to ligand chemistry, suggest possible molecular determinants of recognition, with implications regarding intracellular BA transport. Our findings suggest that human L-FABP is a poorly selective, universal BA binder. PMID:25639618

  19. Effects of calcium salts of acidic monomers on mineral induction of phosphoprotein immobilized to agarose beads.

    PubMed

    Ito, Shuichi; Iijima, Masahiro; Motai, Fumiko; Mizoguchi, Itaru; Saito, Takashi

    2012-10-01

    The aim of this study is to evaluate the mineralizing potential of acidic monomers and their calcium salts for mineralization, using an in vitro mineral induction model. Phosvitin (PV) was used as a model phosphoprotein in this study. PV was immobilized on agarose beads with divinyl sulfone. Five aliquots of agarose-immobilized PV, acidic monomers, and their calcium salts were incubated in mineralizing solution at various concentrations. The PV beads and acidic monomers were incubated at 37°C. Samples were taken at several time points during the incubation. Then, the agarose beads were analyzed for bound calcium by atomic absorption spectrometry. The mineral formed on the agarose beads was identified as an apatite by microarea X-ray diffraction. Additionally, the specimens were observed using scanning electron microscopy (SEM). Mineral induction time decreased with increasing solution saturation. 4-METCa salt [calcium salt of 4-methacryloxyethyl trimellitate (CMET)] significantly reduced the mineral induction time. Using these data, the interfacial tension for mineral induction of PV and CMET was determined to be 90.1 and 92.7 ergs/cm(2), respectively. The mineral induced in each specimen after incubation for 24 h was identified by its X-ray diffraction pattern as apatite. SEM observation showed that lath-shaped crystals were formed on the surfaces of the CMET. We conclude that CMET could play a role in dentin remineralization. PMID:22623052

  20. Length Scale Dependence of the Dynamic Properties of Hyaluronic Acid Solutions in the Presence of Salt

    SciTech Connect

    Horkay, Ferenc; Falus, Peter; Hecht, Anne-Marie; Geissler, Erik

    2010-12-07

    In solutions of the charged semirigid biopolymer hyaluronic acid in salt-free conditions, the diffusion coefficient D{sub NSE} measured at high transfer momentum q by neutron spin echo is more than an order of magnitude smaller than that determined by dynamic light scattering, D{sub DLS}. This behavior contrasts with neutral polymer solutions. With increasing salt content, D{sub DLS} approaches D{sub NSE}, which is independent of ionic strength. Contrary to theoretical expectation, the ion-polymer coupling, which dominates the low q dynamics of polyelectrolyte solutions, already breaks down at distance scales greater than the Debye-Hueckel length.

  1. Diffusion dialysis. Effect of membrane composition on acid/salt separation

    SciTech Connect

    Narebska, A.; Warszawski, A. )

    1992-05-01

    Diffusion dialysis is an energy-saving separation technique. In order to highlight the relationship between membrane composition and ability to separate acid/salt mixtures by diffusion dialysis, a few anion-exchange membranes were examined. Experiments on solubility/diffusivity phenomena were carried out in contact with hydrochloric acid and sodium chloride solutions (single- and two-solute experiments). Computations using Glueckauf and Tye models have indicated high nonuniformity in the distribution of fixed charged within the membranes and different accessibilities of the internal membrane volumes for the acid and salt. The Neosepta AFN-7 membrane (Tokuymam Soda Co.) has proved effective in differentiating the permeants by sorption (k{sub HCl}/k{sub NaCl} {approx} 2) and diffusivity ({bar D}{sub HCl}/{bar D}{sub NaCl} up to 10). This membrane is also the only one which, when in contact with two-solutes solutions, absorbs the acid preferentially to the salt. For this membrane the preferential sorption and transport of the acid depends not only on the physical structure of the membrane but also on the chemical nature of the polymer which contains pyridine moieties.

  2. Lithium and cesium acidities of some terminal acethylenes and aggregation of their salts in tetrahydrofuran

    SciTech Connect

    Gareyev, R.; Streitwieser, A.

    1995-12-01

    Ion-pair acidity equilibria have been determined for 4-ethynylbiphenyl (1), 1-ethynyladamantane (2) and 3,3,3-triphenylpropyne (3) with lithium and cesium as counterions in tetrahydrofuran. The pK values increase, 1 < 3 < 2, with lithium as the counterion. With the cesium gegenion the pK of compound 2 is also higher than that of 3. The cesium salt of 1 is insoluble in tetrahydrofuran. Comparison of lithium and cesium acidities shows a difference of 6 pK units for both 2 and 3, the lithium pK being lower. In some cases, the measured equilibrium acidities depend on the concentration of the acetylene salt, which indicates aggregation of ion pairs into higher ionic clusters. The average aggregation numbers were determined from the equilibrium studies.

  3. Mathematical modeling of acid deposition due to radiation fog

    SciTech Connect

    Pandis, S.N.; Seinfeld, J.H. )

    1989-09-20

    A Lagrangian model has been developed to study acidic deposition due to radiation fog. The model couples submodels describing the development and dissipation of radiation fog, the gas-phase chemistry and transfer, and the aqueous-phase chemistry. The model is applied to a radiation fog episode in Bakersfield in the San Joaquin Valley of California over the period January 4--5 1985. Model predictions for temperature profile, fog development, liquid water content, gas-phase concentrations of SO{sub 2}, HNO{sub 3}, and NH{sub 3}, {ital p}H, aqueous-phase concentrations of OS{sup 2{minus}}{sub 4}, NH{sup +}{sub 4}, and NO{sup {minus}}{sub 3}, and finally deposition rates of the above ions are compared with the observed values. The deposition rates of the major ions are predicted to increase significantly during the fog episode, the most notable being the increase of sulfate deposition. Pathways for sulfate production that are of secondary importance in a cloud environment may become signficant in a fog. Expressing the mean droplet settling velocity as a function of liquid water content is found to be quite influential in the model's predictions. {copyright} American Geophysical Union 1989

  4. Acid Deposition From Stratospheric Geoengineering With Sulfate Aerosols

    NASA Astrophysics Data System (ADS)

    Kravitz, B.; Robock, A.; Oman, L.; Stenchikov, G.

    2008-12-01

    We used a general circulation model of the Earth's climate to conduct geoengineering experiments involving stratospheric injection of sulfur dioxide [Robock et al., 2008] and analyzed the resulting deposition of sulfate. When sulfur is injected into the tropical or Arctic stratosphere, the main additional surface deposition occurs in midlatitude bands, because of strong cross-tropopause flux in the jet stream regions, and there are some larger local increases, specifically in Northern Canada and the Western Pacific Ocean. We used critical load studies to determine the effects of this increase in acid deposition on terrestrial ecosystems. For annual injection of 5 Tg of SO2 into the tropical stratosphere or 3 Tg of SO2 into the Arctic stratosphere, the additional surface sulfate deposition is not enough to negatively impact most ecosystems. Robock, Alan, Luke Oman, and Georgiy Stenchikov (2008), Regional climate responses to geoengineering with tropical and Arctic SO2 injections. J. Geophys. Res., 113, D16101, doi:10.1029/2008JD010050.

  5. Electrolyte salts for power sources

    DOEpatents

    Doddapaneni, N.; Ingersoll, D.

    1995-11-28

    Electrolyte salts are disclosed for power sources comprising salts of phenyl polysulfonic acids and phenyl polyphosphonic acids. The preferred salts are alkali and alkaline earth metal salts, most preferably lithium salts. 2 figs.

  6. Mitigation of acid deposition: Liming of surface waters. Final report

    SciTech Connect

    Bartoshesky, J.; Price, R.; DeMuro, J.

    1989-05-01

    In recent years acid deposition has become a serious concern internationally. Scientific literature has documented the acidification of numerous lakes and streams in North America and Scandinavia resulting in the depletion or total loss of fisheries and other aquatic biota. Liming represents the only common corrective practice aimed specifically at remediating an affected acid receptor. This report reviews a range of liming technologies and liming materials, as well as the effect of surface-water liming on water quality and aquatic biota. As background to the liming discussion, the hydrologic cycle and the factors that make surface waters sensitive to acid deposition are also discussed. Finally, a brief review of some of the liming projects that have been conducted, or are currently in operation is presented, giving special emphasis to mitigation efforts in Maryland. Liming has been effectively used to counteract surface-water acidification in parts of Scandinavia, Canada, and the U.S. To date, liming has generally been shown to improve physical and chemical conditions and enhance the biological recovery of aquatic ecosystems affected by acidification.

  7. Polyglycolic acid microneedles modified with inkjet-deposited antifungal coatings.

    PubMed

    Boehm, Ryan D; Daniels, Justin; Stafslien, Shane; Nasir, Adnan; Lefebvre, Joe; Narayan, Roger J

    2015-01-01

    In this study, the authors examined use of piezoelectric inkjet printing to apply an antifungal agent, voriconazole, to the surfaces of biodegradable polyglycolic acid microneedles. Polyglycolic acid microneedles with sharp tips (average tip radius = 25 ± 3 μm) were prepared using a combination of injection molding and drawing lithography. The elastic modulus (9.9 ± 0.3 GPa) and hardness (588.2 ± 33.8 MPa) values of the polyglycolic acid material were determined using nanoindentation and were found to be suitable for use in transdermal drug delivery devices. Voriconazole was deposited onto the polyglycolic acid microneedles by means of piezoelectric inkjet printing. It should be noted that voriconazole has poor solubility in water; however, it is readily soluble in many organic solvents. Optical imaging, scanning electron microscopy, energy dispersive x-ray spectrometry, and Fourier transform infrared spectroscopy were utilized to examine the microneedle geometries and inkjet-deposited surface coatings. Furthermore, an in vitro agar plating study was performed on the unmodified, vehicle-modified, and voriconazole-modified microneedles. Unlike the unmodified and vehicle-modified microneedles, the voriconazole-modified microneedles showed antifungal activity against Candida albicans. The unmodified, vehicle-modified, and voriconazole-modified microneedles did not show activity against Escherichia coli, Pseudomonas aeruginosa, or Staphylococcus aureus. The results indicate that piezoelectric inkjet printing may be useful for loading transdermal drug delivery devices such as polyglycolic acid microneedles with antifungal pharmacologic agents and other pharmacologic agents with poor solubility in aqueous solutions. PMID:25732934

  8. Process for the preparation of 3,4-dihydroxybutanoic acid and salts thereof

    DOEpatents

    Hollingsworth, Rawle I.

    1994-01-01

    A process for the preparation of 3,4-dihydroxybutanoic acid (1) and salts thereof from a glucose source containing 1,4-1inked glucose as a substituent is described. The process uses an alkali metal hdyroxide and hydrogen peroxide to convert the glucose source to (1). The compound (1) is useful as a chemical intermediate to naturally occurring fatty acids and is used to prepare 3,4-dihydroxybutanoic acid-gamma-lactone (2) and furanone (3), particularly stereoisomers of these compounds.

  9. Experimental and theoretical deposition rates from salt-seeded combustion gases of a Mach 0.3 burner rig

    NASA Technical Reports Server (NTRS)

    Santoro, G. J.; Kohl, F. J.; Stearns, C. A.; Gokoglu, S. A.; Rosner, D. E.

    1984-01-01

    Deposition rates on platinum-rhodium cylindrical collectors rotating in the cross streams of the combustion gases of a salt-seeded Mach 0.3 burner rig were determined. The collectors were internally air cooled so that their surface temperatures could be widely varied while they were exposed to constant combustion gas temperatures. The deposition rates were compared with those predicted by the chemically frozen boundary layer (CFBL) computer program, which is based on multicomponent vapor transport through the boundary layer. Excellent agreement was obtained between theory and experiment for the NaCl-seeded case, but the agreement lessened as the seed was changed to synthetic sea salt, NaNO3, and K2SO4, respectively, and was particularly poor in the case of Na2SO4. However, when inertial impaction was assumed to be the deposition mechanism for the Na2SO4 case, the predicted rates agreed well with the experimental rates. The former were calculated from a mean particle diameter that was derived from the measured intial droplet size distribution of the solution spray. Critical experiments showed that liquid phase deposits were blown off the smooth surface of the platinum-rhodium collectors by the aerodynamic shear forces of the high-velocity combustion gases but that rough or porous surfaces retained their liquid deposits.

  10. Acid deposition in aquatic ecosystems: Setting limits empirically

    NASA Astrophysics Data System (ADS)

    Newcombe, Charles P.

    1985-07-01

    The problem of acid deposition and its harmful effects on aquatic ecosystems has created a new branch of science that is called upon to provide the knowledge on which legislative controls can be based. However, because of the nature of existing legislation, which requires evidence of cause and effect between industrial emissions and pollution, and because of science's inability to provide this information over the short term, considerable controversy has arisen about whether sufficient information exists to warrant control measures at this time. Among those who advocate controls, there is genuine divergence of opinion about how stringent the controls must be to achieve any desired level of protection. The controversy has led to an impasse between the scientific and political participants, which is reflected in the slow pace of progress toward an effective management strategy. Resolution of the impasse, at least in the short term, may demand that science and politics rely on empirical models rather than explanatory ones. The empirical model, which is the major proposal in this article, integrates all of the major variables and many of the minor ones, and constructs a three-dimensionally curved surface capable of representing the status of any waterbody subjected to the effects of acid deposition. When suitably calibrated—a process involving the integration of knowledge and data from aquatic biology, geochemistry, meteorology, and limnology—it can be used to depict limits to the rate of acid deposition required for any level of environmental protection. Because it can generate a pictorial display of the effects of management decisions and legislative controls, the model might serve as a basis for enhancing the quality of communication among all the scientific and political participants and help to resolve many of their controversies.

  11. Infrared thermography of evaporative fluxes and dynamics of salt deposition on heterogeneous porous surfaces

    NASA Astrophysics Data System (ADS)

    Nachshon, Uri; Shahraeeni, Ebrahim; Or, Dani; Dragila, Maria; Weisbrod, Noam

    2011-12-01

    Evaporation of saline solutions from porous media, common in arid areas, involves complex interactions between mass transport, energy exchange and phase transitions. We quantified evaporation of saline solutions from heterogeneous sand columns under constant hydraulic boundary conditions to focus on effects of salt precipitation on evaporation dynamics. Mass loss measurements and infrared thermography were used to quantify evaporation rates. The latter method enables quantification of spatial and temporal variability of salt precipitation to identify its dynamic effects on evaporation. Evaporation from columns filled with texturally-contrasting sand using different salt solutions revealed preferential salt precipitation within the fine textured domains. Salt precipitation reduced evaporation rates from the fine textured regions by nearly an order of magnitude. In contrast, low evaporation rates from coarse-textured regions (due to low capillary drive) exhibited less salt precipitation and consequently less evaporation rate suppression. Experiments provided insights into two new phenomena: (1) a distinct increase in evaporation rate at the onset of evaporation; and (2) a vapor pumping mechanism related to the presence of a salt crust over semidry media. Both phenomena are related to local vapor pressure gradients established between pore water and the surface salt crust. Comparison of two salts: NaCl and NaI, which tend to precipitate above the matrix surface and within matrix pores, respectively, shows a much stronger influence of NaCl on evaporation rate suppression. This disparity reflects the limited effect of NaI precipitation on matrix resistivity for solution and vapor flows.

  12. Alleviation of salt-induced oxidative damage by 5-aminolevulinic acid in wheat seedlings

    NASA Astrophysics Data System (ADS)

    Genişel, Mucip; Erdal, Serkan

    2016-04-01

    The aim of this study was to elucidate how 5-aminolevulinic acid (ALA), the precursor of chlorophyll compounds, affects the defence mechanisms of wheat seedlings induced by salt stress. To determine the possible stimulative effects of ALA against salinity, 11-day old wheat seedlings were sprayed with ALA at two different concentrations (10 and 20 mg.l-1) and then stressed by exposure to salt (150 mM NaCl). The salt stress led to significant changes in the antioxidant activity. While guaiacol peroxidase activity decreased, the activities of superoxide dismutase, catalase, and ascorbate peroxidase markedly increased under salt stress. Compared to the salt stress alone, the application of ALA beforehand further increased the activity of these enzymes. This study is the first time the effects of ALA have been monitored with regard to protein content and the isoenzyme profiles of the antioxidant enzymes. Although the salt stress reduced both the soluble protein content and protein band intensities, pre-treating with ALA significantly mitigated these stress-induced reductions. The data for the isoenzyme profiles of the antioxidant enzymes paralleled that of the ALA-induced increases in antioxidant activity. As a consequence of the high antioxidant activity in the seedlings pre-treated with ALA, the stress-induced elevations in the reactive oxygen species, superoxide anion, and hydrogen peroxide contents and lipid peroxidation levels were markedly diminished. Taken together, this data demonstrated that pre-treating with ALA confers resistance to salt stress by modulating the protein synthesis and antioxidant activity in wheat seedlings.

  13. 40 CFR 721.2140 - Carbo-poly-cycli-col azo-alkyl-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt. 721.2140 Section 721.2140 Protection of Environment...-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt. (a) Chemical substance and significant new uses...-mino-al-kyl-car-bo-mon-o-cyc-lic ester, halogen acid salt (PMN P-88-1682) is subject to reporting...

  14. 40 CFR 721.2140 - Carbo-poly-cycli-col azo-alkyl-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt. 721.2140 Section 721.2140 Protection of Environment...-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt. (a) Chemical substance and significant new uses...-mino-al-kyl-car-bo-mon-o-cyc-lic ester, halogen acid salt (PMN P-88-1682) is subject to reporting...

  15. 40 CFR 721.2140 - Carbo-poly-cycli-col azo-alkyl-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt. 721.2140 Section 721.2140 Protection of Environment...-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt. (a) Chemical substance and significant new uses...-mino-al-kyl-car-bo-mon-o-cyc-lic ester, halogen acid salt (PMN P-88-1682) is subject to reporting...

  16. 40 CFR 721.2140 - Carbo-poly-cycli-col azo-alkyl-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt. 721.2140 Section 721.2140 Protection of Environment...-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt. (a) Chemical substance and significant new uses...-mino-al-kyl-car-bo-mon-o-cyc-lic ester, halogen acid salt (PMN P-88-1682) is subject to reporting...

  17. 40 CFR 721.2140 - Carbo-poly-cycli-col azo-alkyl-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt. 721.2140 Section 721.2140 Protection of Environment...-aminoalkyl-carbo-mono-cyclic ester, halogen acid salt. (a) Chemical substance and significant new uses...-mino-al-kyl-car-bo-mon-o-cyc-lic ester, halogen acid salt (PMN P-88-1682) is subject to reporting...

  18. 40 CFR 180.1284 - Ammonium salts of higher fatty acids (C8-C18 saturated; C8-C12 unsaturated); exemption from the...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 24 2011-07-01 2011-07-01 false Ammonium salts of higher fatty acids... Ammonium salts of higher fatty acids (C8-C18 saturated; C8-C12 unsaturated); exemption from the requirement of a tolerance. Ammonium salts of C8-C18 saturated and C8-C12 unsaturated higher fatty acids...

  19. 40 CFR 180.1284 - Ammonium salts of higher fatty acids (C8-C18 saturated; C8-C12 unsaturated); exemption from the...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 23 2010-07-01 2010-07-01 false Ammonium salts of higher fatty acids... Ammonium salts of higher fatty acids (C8-C18 saturated; C8-C12 unsaturated); exemption from the requirement of a tolerance. Ammonium salts of C8-C18 saturated and C8-C12 unsaturated higher fatty acids...

  20. Distribution and effects of acidic deposition on wildlife and ecosystems

    USGS Publications Warehouse

    Stromborg, K.L.; Longcore, J.R.

    1987-01-01

    Acidic deposition occurs over most of the United States and the deposition patterns and theoretical vulnerabilities of aquatic ecosystems to chemical changes can be delineated, but few data exist on concomitant biological effects. Hypothetical direct effects are limited primarily to toxicity of various heavy metals mobilized at reduced pH. Results of studies in Scandinavia suggest that aluminum interferes with avian reproduction near acidified lakes. Some amphibian populations located on acid-vulnerable substrates may be adversely affected by reduced pH in the vernal pools used for egg laying and larval growth. Indirect effects on populations are difficult to detect because few historical data exist for wildlife populations and trophic relationships in vulnerable areas. Current research in the U.S.A. focuses on measuring habitat characteristics, food availability, and avian use of vulnerable wetland habitats. Results of Scandinavian studies suggest that some species of waterfowl may prefer acidified, I fish-free habitats because invertebrates essential for meeting nutritional requirements are more easily obtained in the absence of competition from fish. However, avian species dependent on fish would be absent from these habitats. Alteration of either the vegetative structure or primary productivity of wetlands might indirectly affect avian populations by causing decreased invertebrate productivity and consequent food limitations for birds.

  1. Radiation curing of polyester resin modified with acrylic acid and its salts

    NASA Astrophysics Data System (ADS)

    Szalińska, H.; Pietrzak, M.; Janowska, G.

    Polyester resin containing acrylic acid or its salts was cured with γ 60Co radiation. The course of curing was examined, the gel content and polymerization shrinkage were measured and also thermographic and IR absorption analyses were carried out. It was found that manganese, iron and copper acrylates inhibited the curing of resin while the remaining additives showed a slightly stimulating action. All the additives decreased the polymerization shrinkage by a factor of 2-3 and iron acrylate by as much as 8 times (up to 1%). They also increased the activation energy of the thermal decomposition of resin, and calcium, barium and copper acrylates increased the thermal stability of resin by 20 K. IR absorption spectra showed that acrylic acid and its salts reacted mainly with the monomeric component of the resin (styrene) whereas iron and copper acrylates first attacked the unsaturated bonds of the oligoester.

  2. [Psychotropic effect of phenibut salts and their compositions with organic acids].

    PubMed

    Tiurenkov, I N; Bagmetova, V V; Krivitskaia, A N; Berestovitskaia, V M; Vasil'eva, O S

    2011-01-01

    The spectra of psychotropic action of some phenibut salts (succunate, maleate, nicotinate) and a composition of phenibut with glutamic acid were studied. It is established, that the substances studied show psychotropic activity spectrum generally similar to that of phenibut, but different in expressiveness of some particular effects. Compound RSPU-149 exhibited the most pronounced psychotropic action: its anxiolytic effect was below, the antidepressant effect was comparable with, and the nootrope action exceeded that of phenibut. PMID:21476277

  3. Amine salt of n-triazolyl-hydrocarbyl succinamic acid and lubricating oil composition containing same

    SciTech Connect

    Nebzydoski, J.W.; Patmore, E.L.

    1981-08-11

    An amine salt of n-triazolyl-hydrocarbyl succinamic acid represented by the formula: 3-(HOOC-R''''-CO-NH-)-1,2,4-triazole. R'''-NH-R''' in which R'''' is an alkylene radical having from 2 to 24 carbon atoms and R''' is hydrogen or a hydrocarbyl radical having from 1 to 24 carbon atoms at least one R''' being a hydrocarbyl radical and a lubricating oil composition containing same is provided.

  4. Supported phosphate and carbonate salts for heterogeneous catalysis of triglycerides to fatty acid methyl esters

    NASA Astrophysics Data System (ADS)

    Britton, Stephanie Lynne

    Fatty acid methyl esters made from vegetable oil, or biodiesel, have been identified as a substitute for diesel derived from crude oil. Biodiesel is currently made using a homogeneous base catalyst to perform the transesterification of triglycerides with methanol to generate fatty acid methyl esters (FAME). The use of a homogeneous catalyst necessitates additional purification of the product and byproducts before sale, and the catalyst is consumed and discarded. The development of a heterogeneous basic catalyst for the production of FAME is desirable. Tribasic phosphate salts and dibasic carbonate salts are active for the production of FAME but generally operate as homogeneous catalysts. Supporting these phosphate and carbonate salts on mesoporous MCM-41, microporous silica gel, and nonporous a-alumina proved successful to greater or lesser degrees depending on the identity of the support and pretreatment of the support. Although these salts were supported and were active for the production of FAME from canola oil, they proved to be operating as homogeneous catalysts due to leaching of the active species off the surface of the support. Further investigation of the active species present in the tribasic phosphate catalysts identified the active support as orthophosphate, and NMR studies revealed the phosphorus to be present as orthophosphate and diphosphate in varying proportions in each catalyst. Evaluation of the acid-washing support pretreatment process revealed that the exposure of the support to acid plays a large role in the development of activity on the surface of the catalyst, but manipulation of these parameters did not prevent leaching of the active site off the surface of the catalyst. Alternate methods of support pretreatment were no more effective in preventing leaching. Tribasic phosphate supported on silica gel is not effective as a heterogeneous catalyst for FAME production from triglycerides because of the lack of stability of the phosphate on the

  5. Reactions Between Water Soluble Organic Acids and Nitrates in Atmospheric Aerosols: Recycling of Nitric Acid and Formation of Organic Salts

    SciTech Connect

    Wang, Bingbing; Laskin, Alexander

    2014-03-25

    Atmospheric particles often include a complex mixture of nitrate and secondary organic materials accumulated within the same individual particles. Nitrate as an important inorganic component can be chemically formed in the atmosphere. For instance, formation of sodium nitrate (NaNO3) and calcium nitrate Ca(NO3)2 when nitrogen oxide and nitric acid (HNO3) species react with sea salt and calcite, respectively. Organic acids contribute a significant fraction of photochemically formed secondary organics that can condense on the preexisting nitrate-containing particles. Here, we present a systematic microanalysis study on chemical composition of laboratory generated particles composed of water soluble organic acids and nitrates (i.e. NaNO3 and Ca(NO3)2) investigated using computer controlled scanning electron microscopy with energy dispersive analysis of X-rays (CCSEM/EDX) and Fourier transform infrared micro-spectroscopy (micro-FTIR). The results show that water-soluble organic acids can react with nitrates releasing gaseous HNO3 during dehydration process. These reactions are attributed to acid displacement of nitrate with weak organic acids driven by the evaporation of HNO3 into gas phase due to its relatively high volatility. The reactions result in significant nitrate depletion and formation of organic salts in mixed organic acids/nitrate particles that in turn may affect their physical and chemical properties relevant to atmospheric environment and climate. Airborne nitrate concentrations are estimated by thermodynamic calculations corresponding to various nitrate depletions in selected organic acids of atmospheric relevance. The results indicate a potential mechanism of HNO3 recycling, which may further affect concentrations of gas- and aerosol-phase species in the atmosphere and the heterogeneous reaction chemistry between them.

  6. 40 CFR 721.5252 - 2-Naphthalenecarboxylic acid, 4,4′-methylenebis [3-hydroxy-, zinc salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...-methylenebis [3-hydroxy-, zinc salt. 721.5252 Section 721.5252 Protection of Environment ENVIRONMENTAL...′-methylenebis [3-hydroxy-, zinc salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as 2-Naphthalenecarboxylic acid, 4,4′-methylenebis [3-hydroxy-,...

  7. 40 CFR 721.5252 - 2-Naphthalenecarboxylic acid, 4,4′-methylenebis [3-hydroxy-, zinc salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-methylenebis [3-hydroxy-, zinc salt. 721.5252 Section 721.5252 Protection of Environment ENVIRONMENTAL...′-methylenebis [3-hydroxy-, zinc salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as 2-Naphthalenecarboxylic acid, 4,4′-methylenebis [3-hydroxy-,...

  8. 40 CFR 721.5252 - 2-Naphthalenecarboxylic acid, 4,4′-methylenebis [3-hydroxy-, zinc salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...-methylenebis [3-hydroxy-, zinc salt. 721.5252 Section 721.5252 Protection of Environment ENVIRONMENTAL...′-methylenebis [3-hydroxy-, zinc salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as 2-Naphthalenecarboxylic acid, 4,4′-methylenebis [3-hydroxy-,...

  9. 40 CFR 721.5252 - 2-Naphthalenecarboxylic acid, 4,4′-methylenebis [3-hydroxy-, zinc salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...-methylenebis [3-hydroxy-, zinc salt. 721.5252 Section 721.5252 Protection of Environment ENVIRONMENTAL...′-methylenebis [3-hydroxy-, zinc salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as 2-Naphthalenecarboxylic acid, 4,4′-methylenebis [3-hydroxy-,...

  10. 40 CFR 721.5252 - 2-Naphthalenecarboxylic acid, 4,4′-methylenebis [3-hydroxy-, zinc salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...-methylenebis [3-hydroxy-, zinc salt. 721.5252 Section 721.5252 Protection of Environment ENVIRONMENTAL...′-methylenebis [3-hydroxy-, zinc salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as 2-Naphthalenecarboxylic acid, 4,4′-methylenebis [3-hydroxy-,...

  11. 77 FR 33399 - Citric Acid and Certain Citrate Salts From the People's Republic of China: Preliminary Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-06-06

    ... Administrative Review, 77 FR 1455 (January 10, 2012). \\10\\ See Citric Acid and Certain Citrate Salts from the... Certain Citrate Salts from Canada and the People's Republic of China: Antidumping Duty Orders, 74 FR 25703... Request for Revocation in Part, 76 FR 37781, 37785 (June 28, 2011) (``Initiation''). \\3\\ See Letter...

  12. Taxonomic homogeneity of a salt-tolerant lactic acid bacteria isolated from shoyu mash.

    PubMed

    Hanagata, Hiroshi; Shida, Osamu; Takagi, Hiroaki

    2003-04-01

    Forty-seven salt-tolerant lactic acid bacteria, which had been isolated from different places and grown in 15% NaCl, were examined to assess their taxonomic heterogeneity. Among the isolates, 42 were isolated from shoyu mash during the acid fermentation phase, 2 were from miso and 3 were from anchovy pickles. All isolates were identified as Tetragenococcus halophilus on the basis of DNA relatedness values. We further examined 102 phenotypic characteristics of them. The isolates exhibited differences in only 16, supporting the conclusion obtained from the DNA relatedness analysis. PMID:12833212

  13. Oleate salt formation and mesomorphic behavior in the propranolol/oleic acid binary system.

    PubMed

    Crowley, K J; Forbes, R T; York, P; Nyqvist, H; Camber, O

    1999-06-01

    Thermal analysis of propranolol/oleic acid mixtures prepared by solvent evaporation enabled construction of the binary system phase diagram. This allowed both physical and chemical interactions to be identified, including complex formation at the equimolar composition. An incongruent melting complex with a characteristic reaction point was identified in excess oleic acid compositions, a common property of fatty acid/fatty acid salt binary systems. The equimolar complex was confirmed to be propranolol oleate using infrared spectroscopy. Wide-angle X-ray powder diffractometry demonstrated that propranolol oleate possessed long-range positional order ( approximately 25 A d spacing) accompanied by a degree of disorder over shorter d spacings. Such a pattern suggested mesophase formation, explaining the unctuous nature of propranolol oleate at room temperature. Accurate measurement of the long-range d spacing was achieved using small-angle X-ray scattering, permitting differentiation of the three different phases identified (phase I: 25.4 A, phase II: 24.6 A, phase III: 25.4-25.5 A). The implications of drug fatty acid salt formation and also mesomorphism in pharmaceutical systems are discussed. PMID:10350493

  14. Buffering effects of calcium salts in kimchi: lowering acidity, elevating lactic acid bacterial population and dextransucrase activity.

    PubMed

    Chae, Seo Eun; Moon, Jin Seok; Jung, Jee Yun; Kim, Ji-Sun; Eom, Hyun-Ju; Kim, So-Young; Yoon, Hyang Sik; Han, Nam Soo

    2009-12-01

    This study investigates the buffering effects of calcium salts in kimchi on total acidity, microbial population, and dextransucrase activity. Calcium chloride or calcium carbonate was added in dongchimi-kimchi, a watery-radish kimchi, and their effects on various biochemical attributes were analyzed. The addition of 0.1% calcium chloride produced a milder decrease in the pH after 24 days of incubation, which allowed the lactic acid bacteria to survive longer than in the control. In particular, the heterofermentative Leuconostoc genus population was 10-fold higher than that in the control. When sucrose and maltose were also added along with the calcium salts, the dextransucrase activity in the kimchi was elevated and a higher concentration of isomaltooligosaccharides was synthesized when compared with the control. Calcium chloride was determined as a better activator compound of dextransucrase than calcium carbonate, probably because of its higher solubility. Therefore, the results of this study confirm the ability of the proposed approach to modulate the kimchi fermentation process and possibly enhance the quality of kimchi based on the addition of dietary calcium salts. PMID:20075632

  15. 40 CFR 180.1121 - Boric acid and its salts, borax (sodium borate decahydrate), disodium octaborate tetrahydrate...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 24 2011-07-01 2011-07-01 false Boric acid and its salts, borax... EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES IN FOOD Exemptions From Tolerances § 180.1121 Boric acid and its... the requirement of a tolerance is established for residues of the pesticidal chemical boric acid...

  16. 40 CFR 180.1121 - Boric acid and its salts, borax (sodium borate decahydrate), disodium octaborate tetrahydrate...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 25 2012-07-01 2012-07-01 false Boric acid and its salts, borax... EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES IN FOOD Exemptions From Tolerances § 180.1121 Boric acid and its... the requirement of a tolerance is established for residues of the pesticidal chemical boric acid...

  17. 40 CFR 180.1121 - Boric acid and its salts, borax (sodium borate decahydrate), disodium octaborate tetrahydrate...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 23 2010-07-01 2010-07-01 false Boric acid and its salts, borax... EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES IN FOOD Exemptions From Tolerances § 180.1121 Boric acid and its... the requirement of a tolerance is established for residues of the pesticidal chemical boric acid...

  18. 40 CFR 180.1121 - Boric acid and its salts, borax (sodium borate decahydrate), disodium octaborate tetrahydrate...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 25 2013-07-01 2013-07-01 false Boric acid and its salts, borax... EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES IN FOOD Exemptions From Tolerances § 180.1121 Boric acid and its... the requirement of a tolerance is established for residues of the pesticidal chemical boric acid...

  19. 40 CFR 180.1121 - Boric acid and its salts, borax (sodium borate decahydrate), disodium octaborate tetrahydrate...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 24 2014-07-01 2014-07-01 false Boric acid and its salts, borax... EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES IN FOOD Exemptions From Tolerances § 180.1121 Boric acid and its... the requirement of a tolerance is established for residues of the pesticidal chemical boric acid...

  20. Catalytic actions of alkaline salts in reactions between 1,2,3,4-butanetetracarboxylic acid and cellulose: II. Esterification.

    PubMed

    Ji, Bolin; Tang, Peixin; Yan, Kelu; Sun, Gang

    2015-11-01

    1,2,3,4-Butanetetracarboxylic acid (BTCA) reacts with cellulose in two steps with catalysis of alkaline salts such as sodium hypophosphite: anhydride formation and esterification of anhydride with cellulose. The alkali metal ions were found effective in catalyzing formation of BTCA anhydride in a previous report. In this work, catalytic functions of the alkaline salts in the esterification reaction between BTCA anhydride and cellulose were investigated. Results revealed that acid anions play an important role in the esterification reaction by assisting removal of protons on intermediates and completion of the esterification between cellulose and BTCA. Besides, alkaline salts with lower pKa1 values of the corresponding acids are more effective ones for the reaction since addition of these salts could lead to lower pH values and higher acid anion concentrations in finishing baths. The mechanism explains the results of FTIR and wrinkle recovery angles of the fabrics cured under different temperatures and times. PMID:26256345

  1. Biphasic dissolution method for quality control and assurance of drugs containing active substances in the form of weak acid salts.

    PubMed

    Franc, Aleš; Muselłk, Jan; Goněc, Roman; Vetchý, David

    2016-03-01

    Substances in the form of weak acid salts have been found to be problematic for dissolution testing. Their absorption can start only after they are turned into the form of an acid following the gastric passage although they were administered in the form of a salt. Due to poor solubility, they cannot be tested in acidic gastric environment for a biased dissolution profile. The biphasic dissolution method is promising for overcoming this obstacle. Tablets with warfarin clathrate sodium salt in two concentrations and two different particle size distributions were tested as a suitable model for finding the medium and process conditions of dissolution. The dissolution method based on the use of the upper organic layer (1-octanol) and the lower aqueous layer 0.1 mol L(-1) HCl) was found suitable and discriminatory for tablets containing active substances in the form of salts of weak acids. The method also reflects physical differences in the quality of used substances. PMID:26959550

  2. COMPREHENSIVE EXPERIMENTAL DESIGN PLAN TO RELATE POLLUTANT SOURCES TO ACIDIC DEPOSITION

    EPA Science Inventory

    Because verifiable numerical models that incorporate all processes determining the dispersion, transformations, and deposition of emitted pollutants associated with acidic deposition from the atmosphere are only now under development, it was deemed worthwhile to determine whether...

  3. Hydrologic environment of the Silurian salt deposits in parts of Michigan, Ohio, and New York

    USGS Publications Warehouse

    Norris, Stanley E.

    1978-01-01

    The aggregate thickness of evaporites (salt, gypsum, and anhydrite) in the Silurian Salina sequence in Michigan exceeds 1200 feet in areas near the periphery of the Michigan basin, where the salt beds are less than 3000 feet below land surface. In northeast Ohio the aggregate thickness of salt beds is as much as 200 feet in places, and in western New York it is more than 500 feet, where th beds are less than 3000 feet deep. The salt-bearing rocks dip regionally on the order of 50 feet per mile; those in Michigan dip toward the center of the Michigan basin, and those in Ohio and New York, in the Appalachian basin, dip generally southward. The rocks in both basins thicken downdip. Minor folds and faults occur in the salt-bearing rocks in all three states. Some of this defrmation has been attenuated or absorbed bo the salt beds. Occuring near the middle of thick sedimentary sequences, the salt beds are bounded aboe and below by beds containing water having dissolved-solids concentrations several times that seawter. The brines occur commonly in discrete zones of high permeability at specific places in the stratigraphic sequence. In northeast Ohio two prominent brine zones are recognized by the driller, the Devonian Oriskany Sandstone, or 'first water' zone, above the Salina Formation, and the Newburg or 'second water' zone below the Salina. In each aquifer there is a vertical component of hydraulic head, but little brine probably moves through the salt beds because their permeability is extremely low. Also, ther is little evidence of dissolution of the salt in areas distant from the outcrop, suggesting that if brine does move through the salt, movement is at a slow enough rate so that, in combination with the saturated or near-saturated condition of the water, it precludes significant dissolution. Principal brine movement is probably in the permeable zones in the direction of the hydraulic gradient. Two areas in Michigan and one area each in Ohio and New York appear

  4. Crystal and molecular structures of twelve salts from isopropylamine and different organic acids

    NASA Astrophysics Data System (ADS)

    Wen, Xianhong; Zhang, Huan; Xu, Kai; Sun, JiaHui; Ye, Jiaying; Jin, Shouwen; Wang, Daqi

    2015-08-01

    Twelve isopropylamine derived supramolecular complexes isopropylamine: (m-toluic acid) [(Hipa)+ ṡ (mtua-), mtua- = m-toluate] (1), isopropylamine: (p-toluic acid) [(Hipa)+ ṡ (ptua-), ptua- = p-toluate] (2), isopropylamine: (p-methoxybenzoic acid) [(Hipa)+ ṡ (pmba-), pmba- = p-methoxybenzoate] (3), (isopropylamine): (3,4-methylenedioxybenzoic acid) [(Hipa)+ ṡ (mba)-, mba = 3,4-methylenedioxybenzoate] (4), (isopropylamine): (2-methyl-2-phenoxypropanoic acid) [(Hipa)+ ṡ (mpa-), mpa- = 2-methyl-2-phenoxypropionate] (5), (isopropylamine): (4-chlorophenoxyacetic acid) [(Hipa)+ ṡ (cpa-), cpa- = 4-chlorophenoxyacetate] (6), (isopropylamine): (3,5-dinitrobenzoic acid) [(Hipa)+ ṡ (dnba-), dnba- = 3,5-dinitrobenzoate] (7), (isopropylamine): (2-furoic acid) [(Hipa)+ ṡ (fura-), fura- = 2-furoate] (8), (isopropylamine): (1-hydroxy-2-naphthoic acid) [(Hipa)+ ṡ (hna), hna = 1-hydroxy-2-naphthoate] (9), (isopropylamine): (4-nitrophthalic acid) [(Hipa)2+ ṡ (npa2-), npa2- = 4-nitrophthalate] (10), (isopropylamine)2: (2,5-bis-isopropylcarbamoyl-terephthalic acid): 2H2O [(Hipa)2+ ṡ (bta2-) ṡ 2H2O, bta2- = 2,5-bis-isopropylcarbamoyl-terephthalate] (11), and (isopropylamine)2: (1,5-naphthalenedisulfonic acid) [(Hipa)2+ ṡ (nds2-), nds2- = 1,5-naphthalenedisulfonate] (12) were synthesized and structurally characterized by X-ray crystallography. All supramolecular architectures of 1-12 involve extensive classical hydrogen bonds as well as other non-covalent interactions. The results presented herein indicate that the strength and directionality of the Nsbnd H⋯O, Osbnd H⋯O, and Osbnd H⋯S hydrogen bonds between the acidic components and isopropylamine are sufficient to bring about the formation of binary organic salts. The role of weak and strong non-covalent interactions in the crystal packing is ascertained. These weak interactions combined, the complexes 1-12 displayed 1D-3D framework structure.

  5. Steroid binding to Autotaxin links bile salts and lysophosphatidic acid signalling.

    PubMed

    Keune, Willem-Jan; Hausmann, Jens; Bolier, Ruth; Tolenaars, Dagmar; Kremer, Andreas; Heidebrecht, Tatjana; Joosten, Robbie P; Sunkara, Manjula; Morris, Andrew J; Matas-Rico, Elisa; Moolenaar, Wouter H; Oude Elferink, Ronald P; Perrakis, Anastassis

    2016-01-01

    Autotaxin (ATX) generates the lipid mediator lysophosphatidic acid (LPA). ATX-LPA signalling is involved in multiple biological and pathophysiological processes, including vasculogenesis, fibrosis, cholestatic pruritus and tumour progression. ATX has a tripartite active site, combining a hydrophilic groove, a hydrophobic lipid-binding pocket and a tunnel of unclear function. We present crystal structures of rat ATX bound to 7α-hydroxycholesterol and the bile salt tauroursodeoxycholate (TUDCA), showing how the tunnel selectively binds steroids. A structure of ATX simultaneously harbouring TUDCA in the tunnel and LPA in the pocket, together with kinetic analysis, reveals that bile salts act as partial non-competitive inhibitors of ATX, thereby attenuating LPA receptor activation. This unexpected interplay between ATX-LPA signalling and select steroids, notably natural bile salts, provides a molecular basis for the emerging association of ATX with disorders associated with increased circulating levels of bile salts. Furthermore, our findings suggest potential clinical implications in the use of steroid drugs. PMID:27075612

  6. Steroid binding to Autotaxin links bile salts and lysophosphatidic acid signalling

    PubMed Central

    Keune, Willem-Jan; Hausmann, Jens; Bolier, Ruth; Tolenaars, Dagmar; Kremer, Andreas; Heidebrecht, Tatjana; Joosten, Robbie P.; Sunkara, Manjula; Morris, Andrew J.; Matas-Rico, Elisa; Moolenaar, Wouter H.; Oude Elferink, Ronald P.; Perrakis, Anastassis

    2016-01-01

    Autotaxin (ATX) generates the lipid mediator lysophosphatidic acid (LPA). ATX-LPA signalling is involved in multiple biological and pathophysiological processes, including vasculogenesis, fibrosis, cholestatic pruritus and tumour progression. ATX has a tripartite active site, combining a hydrophilic groove, a hydrophobic lipid-binding pocket and a tunnel of unclear function. We present crystal structures of rat ATX bound to 7α-hydroxycholesterol and the bile salt tauroursodeoxycholate (TUDCA), showing how the tunnel selectively binds steroids. A structure of ATX simultaneously harbouring TUDCA in the tunnel and LPA in the pocket, together with kinetic analysis, reveals that bile salts act as partial non-competitive inhibitors of ATX, thereby attenuating LPA receptor activation. This unexpected interplay between ATX-LPA signalling and select steroids, notably natural bile salts, provides a molecular basis for the emerging association of ATX with disorders associated with increased circulating levels of bile salts. Furthermore, our findings suggest potential clinical implications in the use of steroid drugs. PMID:27075612

  7. USING THE REGIONAL ACID DEPOSITION MODEL TO DETERMINE THE NITROGEN DEPOSITION AIRSHED OF THE CHESAPEAKE BAY WATERSHED

    EPA Science Inventory

    The Regional Acid Deposition Model, RADM, an advanced Eulerian model, is used to develop an estimate of the primary airshed of nitrogen oxide (NOx) emissions that is contributing nitrogen deposition to the Chesapeake Bay watershed. rief description of RADM together with a summary...

  8. ACID PRECIPITATION IN NORTH AMERICA: 1985 ANNUAL AND SEASONAL DATA SUMMARIES FROM ACID DEPOSITION SYSTEM DATA BASE

    EPA Science Inventory

    The report gives a summary of 1985 wet deposition precipitation chemistry data collected in North America and available in the Acid Deposition System (ADS) data base. North American wet deposition monitoring networks with data in ADS are NADP/NTN, CANSAP, APN, UAPSP, MAP3S/PCN, W...

  9. Properties of Halococcus salifodinae, an Isolate from Permian Rock Salt Deposits, Compared with Halococci from Surface Waters

    PubMed Central

    Legat, Andrea; Denner, Ewald B. M.; Dornmayr-Pfaffenhuemer, Marion; Pfeiffer, Peter; Knopf, Burkhard; Claus, Harald; Gruber, Claudia; König, Helmut; Wanner, Gerhard; Stan-Lotter, Helga

    2013-01-01

    Halococcus salifodinae BIpT DSM 8989T, an extremely halophilic archaeal isolate from an Austrian salt deposit (Bad Ischl), whose origin was dated to the Permian period, was described in 1994. Subsequently, several strains of the species have been isolated, some from similar but geographically separated salt deposits. Hcc. salifodinae may be regarded as one of the most ancient culturable species which existed already about 250 million years ago. Since its habitat probably did not change during this long period, its properties were presumably not subjected to the needs of mutational adaptation. Hcc. salifodinae and other isolates from ancient deposits would be suitable candidates for testing hypotheses on prokaryotic evolution, such as the molecular clock concept, or the net-like history of genome evolution. A comparison of available taxonomic characteristics from strains of Hcc. salifodinae and other Halococcus species, most of them originating from surface waters, is presented. The cell wall polymer of Hcc. salifodinae was examined and found to be a heteropolysaccharide, similar to that of Hcc. morrhuae. Polyhydroxyalkanoate granules were present in Hcc. salifodinae, suggesting a possible lateral gene transfer before Permian times. PMID:25371342

  10. Properties of Halococcus salifodinae, an Isolate from Permian Rock Salt Deposits, Compared with Halococci from Surface Waters.

    PubMed

    Legat, Andrea; Denner, Ewald B M; Dornmayr-Pfaffenhuemer, Marion; Pfeiffer, Peter; Knopf, Burkhard; Claus, Harald; Gruber, Claudia; König, Helmut; Wanner, Gerhard; Stan-Lotter, Helga

    2013-01-01

    Halococcus salifodinae BIpT DSM 8989T, an extremely halophilic archaeal isolate from an Austrian salt deposit (Bad Ischl), whose origin was dated to the Permian period, was described in 1994. Subsequently, several strains of the species have been isolated, some from similar but geographically separated salt deposits. Hcc. salifodinae may be regarded as one of the most ancient culturable species which existed already about 250 million years ago. Since its habitat probably did not change during this long period, its properties were presumably not subjected to the needs of mutational adaptation. Hcc. salifodinae and other isolates from ancient deposits would be suitable candidates for testing hypotheses on prokaryotic evolution, such as the molecular clock concept, or the net-like history of genome evolution. A comparison of available taxonomic characteristics from strains of Hcc. salifodinae and other Halococcus species, most of them originating from surface waters, is presented. The cell wall polymer of Hcc. salifodinae was examined and found to be a heteropolysaccharide, similar to that of Hcc. morrhuae. Polyhydroxyalkanoate granules were present in Hcc. salifodinae, suggesting a possible lateral gene transfer before Permian times. PMID:25371342

  11. Salt-mediated self-assembly of thioctic acid on gold nanoparticles.

    PubMed

    Volkert, Anna A; Subramaniam, Varuni; Ivanov, Michael R; Goodman, Amanda M; Haes, Amanda J

    2011-06-28

    Self-assembled monolayer (SAM) modification is a widely used method to improve the functionality and stability of bulk and nanoscale materials. For instance, the chemical compatibility and utility of solution-phase nanoparticles are often improved using covalently bound SAMs. Herein, solution-phase gold nanoparticles are modified with thioctic acid SAMs in the presence and absence of salt. Molecular packing density on the nanoparticle surfaces is estimated using X-ray photoelectron spectroscopy and increases by ∼20% when molecular self-assembly occurs in the presence versus the absence of salt. We hypothesize that as the ionic strength of the solution increases, pinhole and collapsed-site defects in the SAM are more easily accessible as the electrostatic interaction energy between adjacent molecules decreases, thereby facilitating the subsequent assembly of additional thioctic acid molecules. Significantly, increased SAM packing densities increase the stability of functionalized gold nanoparticles by a factor of 2 relative to nanoparticles functionalized in the absence of salt. These results are expected to improve the reproducible functionalization of solution-phase nanomaterials for various applications. PMID:21524135

  12. Lead and calcium binding to fulvic acids: Salt effect and competition

    SciTech Connect

    Pinheiro, J.P.; Mota, A.M.; Benedetti, M.F.

    1999-10-01

    Knowledge of the speciation of Pb in natural aquatic systems is important if the authors want to understand the bioavailability and mobility of Pb in polluted and natural environments. The results given in this paper were obtained under conditions as close as possible to natural conditions. These new data show that Pb strongly binds to fulvic acids. The authors also show that the competitive effect of Pb on Ca binding to the same fulvic acid is smaller than the salt effect on Ca binding to fulvic acids as pH varies from 4 to 8. All the data were analyzed with the NICCA-Donnan model developed to describe metal ion binding to natural organic matter. The model predictions of competitive and salt effects are excellent. Comparison of their results with previously published data suggests that metal ion binding strength is similar for fulvic acids from different origins. Thus, all data sets could be interpreted within the framework of a unified modeling approach.

  13. Marked intra-strain variation in response of Listeria monocytogenes dairy isolates to acid or salt stress and the effect of acid or salt adaptation on adherence to abiotic surfaces.

    PubMed

    Adrião, A; Vieira, M; Fernandes, I; Barbosa, M; Sol, M; Tenreiro, R P; Chambel, L; Barata, B; Zilhao, I; Shama, G; Perni, S; Jordan, S J; Andrew, P W; Faleiro, M L

    2008-03-31

    During food processing, and particularly in cheese manufacturing processes, Listeria monocytogenes may be exposed routinely to environments of low pH or high salt concentration. It has been suggested that these environmental conditions may contribute to bacterial adherence to abiotic surfaces and increased resistance to disinfection. In this study strains isolated from the environment of artisanal cheese-making dairies were used to investigate the behaviour of L. monocytogenes in response to acid and salt stress and clear differences between strains was observed. In planktonic culture, strains varied in resistance to low pH or high NaCl concentration and in the occurrence of an adaptive response to moderate acid or NaCl. There was dislocation in responses to salt and acid. Strains resistant, or adaptive, to acid were not resistant or adaptive to NaCl. The reverse also was observed. Exposure to moderate acid did not promote adherence to polystyrene but survival, at low pH or high NaCl concentration, of cells adherent to stainless steel was increased, even for strains that had no adaptive response planktonically, but the detail of these observations varied between strains. In contrast to acid adaptation, with some strains salt adaptation enhanced adherence of L. monocytogenes to polystyrene but this was not true for all strains. For some strains salt- or acid adaptation may enhance the survival of sessile cells exposed to hypochlorite disinfection. PMID:18258322

  14. Effects of texture on salt precipitation dynamics and deposition patterns in drying porous media

    NASA Astrophysics Data System (ADS)

    Norouzi Rad, Mansoureh; Shokri, Nima

    2015-04-01

    Understanding the physics of water evaporation from saline porous media is important in many natural and engineering applications such as durability of building materials and preservation of monuments, CO2 sequestration and water quality. Also excess of salt accumulation in soil may result in soil salinization which is a global problem adversely affecting vegetation, plant growth and crop production. Thus it is important to understand the parameters affecting salt transport and precipitation in porous media. We applied X-ray micro-tomography to investigate the dynamics of salt precipitation during evaporation from porous media as influenced by the particle and pore sizes. The packed beds were saturated with NaCl solution of 3 Molal and the time-lapse X-ray imaging was continued for one day. The results show that the presence of preferential evaporation sites (associated with fine pores) on the surface of the sand columns influences significantly the patterns and dynamics of NaCl precipitation (Norouzi Rad et al., 2013; Norouzi Rad and Shokri, 2014). They confirm the formation of an increasingly thick and discrete salt crust with increasing grain size in the sand column due to the presence of fewer fine pores (preferential precipitation sites) at the surface compared to the sand packs with finer grains. Fewer fine pores on the surface also results in shorter stage-1 precipitation for the columns with larger grain sizes. A simple model for the evolution of salt crust thickness based on this principle shows a good agreement with our experiments. Our results provide new insights regarding the physics of salt precipitation and its complex dynamics in porous media during evaporation. References Norouzi Rad, M., Shokri, N., Sahimi, M. (2013), Pore-Scale Dynamics of Salt Precipitation in Drying Porous Media, Phys. Rev. E, 88, 032404. Norouzi Rad, M., Shokri, N. (2014), Effects of grain angularity on NaCl precipitation in porous media during evaporation, Water Resour. Res

  15. Iridium-Catalyzed ortho-Arylation of Benzoic Acids with Arenediazonium Salts.

    PubMed

    Huang, Liangbin; Hackenberger, Dagmar; Gooßen, Lukas J

    2015-10-19

    In the presence of catalytic [{IrCp*Cl2 }2 ] and Ag2 CO3 , Li2 CO3 as the base, and acetone as the solvent, benzoic acids react with arenediazonium salts to give the corresponding diaryl-2-carboxylates under mild conditions. This C-H arylation process is generally applicable to diversely substituted substrates, ranging from extremely electron-rich to electron-poor derivatives. The carboxylate directing group is widely available and can be removed tracelessly or employed for further derivatization. Orthogonality to halide-based cross-couplings is achieved by the use of diazonium salts, which can be coupled even in the presence of iodo substituents. PMID:26465654

  16. Azetidine-2-carboxylic acid resistant mutants of Arabidopsis thaliana with increased salt tolerance

    SciTech Connect

    Lehle, F.R.; Murphy, M.A.; Khan, R.A. )

    1989-04-01

    Nineteen mutant Arabidopsis families resistant to the proline analog azetidine-2-carboxylic acid (ACA) were characterized in terms of NaCl tolerance and proline content. Mutants were selected from about 64,000 progeny of about 16,000 self-pollinated Columbia parents which had been mutated with ethyl methane sulfonate during seed imbibition. Selections were performed during seed germination on aseptic agar medium containing 0.2 to 0.25 mM ACA. Nineteen mutant families, 12 clearly independent, retained resistance to ACA in the M{sub 4} generation. Based on germination on 150 mM NaCl, 13 of the mutant families were more tolerant than the wild type. Two mutants of intermediate resistance to ACA were markedly more salt tolerant than the others. Four mutant families appeared to overproduce proline. Of these, only 3 showed slight increases in salt tolerance.

  17. Comparative proteomic analysis of β-aminobutyric acid-mediated alleviation of salt stress in barley.

    PubMed

    Mostek, Agnieszka; Börner, Andreas; Weidner, Stanisław

    2016-02-01

    The non-protein amino acid β-aminobutyric acid (BABA) is known to induce plant resistance to a broad spectrum of biotic and abiotic stresses. This is the first study describing the effect of BABA seed priming on physiological and proteomic changes under salt stress conditions in barley (Hordeum vulgare). The aim of our study was to investigate the changes of fresh weight, dry weight and relative water content (RWC) as well as root proteome changes of two barley lines contrasting in salt tolerance (DH14, DH 187) in response to salt stress after seed priming in water or in 800 μM BABA. Seed priming with BABA significantly increased (p ≤ 0.05) RWC in both barley lines, which indicates considerably lower water loss in BABA-primed plants than in the non-primed control plants. Dry and fresh matter increased significantly in line DH 187, whereas no changes were detected in line DH14. BABA-primed plants of both lines showed different proteomic patterns than the non-primed control plants. The root proteins exhibiting significant abundance changes (1.75-fold change, p ≤ 0.05) were separated by two-dimensional polyacrylamide gel electrophoresis (2D- PAGE). Thirty-one spots, representing 24 proteins, were successfully identified by MALDI TOF/TOF mass spectrometry. The most prominent differences include the up-regulation of antioxidant enzymes (catalase, peroxidase and superoxide dismutase), PR proteins (chitinase, endo-1,3-β-glucosidase), and chaperones (cyclophilin, HSC 70). Our results indicate that BABA induces defence and detoxification processes which may enable faster and more effective responses to salt stress, increasing the chances of survival under adverse environmental conditions. PMID:26760953

  18. Al/Pb lightweight grids prepared by molten salt electroless plating for application in lead-acid batteries

    NASA Astrophysics Data System (ADS)

    Hong, Bo; Jiang, Liangxing; Hao, Ketao; Liu, Fangyang; Yu, Xiaoying; Xue, Haitao; Li, Jie; Liu, Yexiang

    2014-06-01

    In this paper, a lightweight Pb plated Al (Al/Pb) grid was prepared by molten salt electroless plating. The SEM and bonding strength test show that the lead coating is deposited with a smooth surface and firm combination. CV test shows that the electrochemical properties of Al/Pb electrodes are stable. 2.0 V single-cell flooded lead-acid batteries with Al/Pb grids as negative collectors are assembled and the performances including 20 h capacity, rate capacity, cycle life, internal resistance are investigated. The results show that the cycle life of Al/Pb-grid cells is about 475 cycles and can meet the requirement of lead-acid batteries. Al/Pb grids are conducive to the refinement of PbSO4 grain, and thereby reduce the internal resistance of battery and advance the utilization of active mass. Moreover, weight of Al/Pb grid is only 55.4% of the conventional-grid. In this way, mass specific capacity of Al/Pb-grid negatives is 17.8% higher and the utilization of active mass is 6.5% higher than conventional-grid negatives.

  19. Structure of six anhydrous molecular salts assembled from noncovalent associations between carboxylic acids and bis-N-imidazoles

    NASA Astrophysics Data System (ADS)

    Jin, Shouwen; Guo, Ming; Wang, Daqi

    2012-08-01

    Six crystalline organic acid-base adducts derived from bis(N-imidazolyl) and carboxylic acids (3,5-dinitrobenzoic acid, 5-nitrosalicylic acid, 3,5-dinitrosalicylic acid, and phthalic acid) were prepared and characterized by X-ray diffraction analysis, IR, mp, and elemental analysis. The six compounds are all organic salts. In salts 1, 2, 4, 5, and 6 the corresponding bis(imidazole) derivatives are diprotonated, while in 3, the corresponding bis(imidazole) derivative is only monoprotonated. All supramolecular architectures of the salts 1-6 involve extensive Nsbnd H⋯O, Osbnd H⋯O, CH⋯O, and CH2⋯O hydrogen bonds as well as other noncovalent interactions. The role of weak and strong noncovalent interactions in the crystal packing is ascertained. All the salts displayed 3D framework structures under the cooperation of these weak interactions. The results presented herein indicate that the strength and directionality of the N+sbnd H⋯O-, Osbnd H⋯O, and Nsbnd H⋯N hydrogen bonds between carboxylic acids and ditopic imidazoles are sufficient to bring about the formation of binary organic salts.

  20. Post-depositional migration and preservation of methanesulfonic acid (MSA) in polar ice cores

    NASA Astrophysics Data System (ADS)

    Osman, M.; Marchal, O.; Guo, W.; Das, S. B.; Evans, M. J.

    2015-12-01

    Methanesulfonic acid (MSA; CH3SO3-) in ice cores is a unique, high-resolution proxy of regional sea ice behavior, marine primary productivity, and synoptic climatology. Significant uncertainties remain, however, in both our understanding of the production and transfer of MSA to the ice sheet, as well as its preservation over time, compromising the paleoclimatological utility of the proxy. Here we apply a numerical modeling approach to quantitatively investigate the post-depositional processes affecting MSA migration and preservation within the firn and ice column, building on recent observational and theoretical studies. Our model allows us to evaluate the timing and magnitude of the vertical movement of MSA in response to varying influences, including the competing effects of 1) concentration gradients of sea-salts typically deposited asynchronously to MSA, 2) snow accumulation and densification rates, and 3) in situ temperature gradients. We first test the model against a recently collected ice core from a high accumulation site in coastal West Antarctica, where monthly-resolved MSA records show an abrupt shift from a summer-to-winter maximum in MSA at ~23m depth (ρ ≈ 650 kg/m3), near the firn-ice transition. We find our model to be a robust predictor of the observed migrational features in this record, capturing both (i) the abrupt shift in summer-to-winter maximal concentrations of MSA (steady state ≈ 3.2 yrs), and (ii) the depression of the seasonal amplitude at depth. Further, our modeling results suggest post-depositional effects can lead to substantial interannual alteration of the MSA signal, contrary to previous assumptions that MSA migration is confined within annual layers at high accumulation sites. Using a broad range of polar MSA records and their associated, site-specific environmental conditions, we will evaluate the fidelity of subannual to interannual variability of MSA records and systematically determine the factors conducive to its

  1. Photosynthetic and growth responses of Schima superba seedlings to sulfuric and nitric acid depositions.

    PubMed

    Yao, Fang-Fang; Ding, Hui-Ming; Feng, Li-Li; Chen, Jing-Jing; Yang, Song-Yu; Wang, Xi-Hua

    2016-05-01

    A continuing rise in acid deposition can cause forest degradation. In China, acid deposition has converted gradually from sulfuric acid deposition (SAD) to nitric acid deposition (NAD). However, the differing responses of photosynthesis and growth to depositions of sulfuric vs. nitric acid have not been well studied. In this study, 1-year-old seedlings of Schima superba, a dominant species in subtropical forests, were treated with two types of acid deposition SO4 (2-)/NO3 (-) ratios (8:1 and 0.7:1) with two applications (foliar spraying and soil drenching) at two pH levels (pH 3.5 and pH 2.5) over a period of 18 months. The results showed that the intensity, acid deposition type, and spraying method had significant effects on the physiological characteristics and growth performance of seedlings. Acid deposition at pH 2.5 via foliar application reduced photosynthesis and growth of S. superba, especially in the first year. Unlike SAD, NAD with high acidity potentially alleviated the negative effects of acidity on physiological properties and growth, probably due to a fertilization effect that improved foliar nitrogen and chlorophyll contents. Our results suggest that trees were damaged mainly by direct acid stress in the short term, whereas in the long term, soil acidification was also likely to be a major risk to forest ecosystems. Our data suggest that the shift in acid deposition type may complicate the ongoing challenge of anthropogenic acid deposition to ecosystem stability. PMID:26797956

  2. [Possibilities of deposition of electrolytes in the skin in different states of water-salt metabolism].

    PubMed

    Arkhibasova, V I; Ivanova, L N; Podsekaeva, G V; Natochin, Iu V

    1983-10-01

    Isotonic solutions of NaCl, KCl or MgCl2 (5 ml/100 g body weight) were introduced into the stomach of rodents. Participation of the skin in the water--salt homeostasis involved a temporal unspecific detaining of ions which were subsequently excreted from the organism. The NaCl and KCl loads increased the amount of exchangeable sodium in the skin structures. A similar response to all the salt loads was observed in abdominal and spinal parts of the skin. PMID:6641985

  3. Modification of fatty acid profile of cow milk by calcium salts of fatty acids and its use in ice cream.

    PubMed

    Nadeem, Muhammad; Abdullah, Muhammad; Hussain, Imtiaz; Inayat, Saima

    2015-02-01

    This study was conducted to determine the effect of calcium salts of fatty acids (CSFA) on fatty acid profile of milk of "Sahiwal" cows and suitability of milk with modified fatty acids in the formulation of ice cream. Fatty acid profile of cow milk was modified by feeding CSFA to eighteen randomly stratified "Sahiwal" cows of first and early lactation divided into three groups. CSFA were offered at two different levels i.e. T1 (150 g per cow per day) T2 (300 g per cow per day) both treatments were compared with a control (T0) without any addition of calcium salts of fatty acids. Iso caloric and iso nitrogenous feeds were given to both experimental groups and control. Concentrations of short chain fatty acids in T0, T1 and T2 were 9.85 ± 0.48a, 8.8 ± 0.24b and 7.1 ± 0.37c %, respectively and the concentrations of C18:1 and C18:2 increased (P < 0.05) from 27.6 ± 1.32b % to 31.7 ± 1.68a % and 2.15 ± 0.09b % to 2.79 ± 0.05a %, respectively, at T2 level. Incorporation of milk fat of T1 and T2 (modified fatty acids profile) in ice cream did not have any adverse effect on pH, acidity and compositional attributes of ice cream. Viscosity of T1 was 67.94 ± 3.77a as compared to (T0) control 68.75 ± 2.46a (CP). Firmness of experimental samples and control were almost similar (P > 0.05) overall acceptability score of T2 was 7.1 ± 0.28b out of 9 (total score) which was more than 78 ± 2.92 %. It was concluded that CSFA may be successfully incorporated up to T2 level (300 g per cow per day) into the feed of "Sahiwal" cows to produce milk with higher content of unsaturated fatty acids and it may be used in the formulation of ice cream with acceptable sensory characteristics and increased health benefits. PMID:25694719

  4. Freezing points and small-scale deicing tests for salts of levulinic acid made from grain sorghum.

    PubMed

    Ganjyal, G; Fang, Q; Hanna, M A

    2007-11-01

    Deicers from renewable resources are needed to overcome the disadvantages of using traditional deicers. Salts made from levulinic acid produced using grain sorghum as raw material were tested as road deicing agents. Freezing points of these salts viz., sodium levulinate, magnesium levulinate and calcium levulinate along with rock salt (sodium chloride) were determined according to American Society for Testing and Materials (ASTM) D 1177-94 standard at concentrations of 10, 20, 30 and 40 % w/w. There were significant differences among the freezing points of the salts. Freezing points for rock salt, sodium levulinate, calcium levulinate and magnesium levulinate, for different concentrations, were in the ranges of -6.6 to -20.5, -2.9 to -15.0, -2.1 to -7.8 and -1.5 to -6.5 degrees C, respectively. Deicing effectiveness of the salts of levulinic acid were investigated by conducting small-scale deicing tests with aqueous solutions of various salt concentrations (2%, 5% and 10%) in a laboratory freezer and by spraying the deicer on a graveled surface covered by ice and snow with the average temperature during the testing at -2.7 degrees C. Deicing capabilities of the three salts of levulinic acid differed. At -2.7 degrees C, all three salts caused melting of the ice. Among the different levulinates studied sodium levulinate was the most effective deicing agent. These salts of levulinates could be a viable replacement for traditional deicers and could help in reducing the disadvantages of traditional deicers. PMID:17416518

  5. Radioluminescence of polyester resin modified with acrylic acid and its salts

    NASA Astrophysics Data System (ADS)

    Szalińska, H.; Wypych, M.; Pietrzak, M.; Szadkowska-Nicze, M.

    Polimal-109 polyester resin and its compounds containing acrylic acid and its salts such as: sodium, potassium, magnesium, calcium, barium, iron, cobalt, copper and manganese acrylates were studied by the radioluminescence method, including isothermal luminescence (ITL) at a radiation temperature of 77 K, thermoluminescence (RTL) and spectral distributions of isothermal luminescence. Measurements of optical absorption at 77 K before and after irradiation of the investigated samples were also carried out. The results obtained have shown that metal ions play a significant part in the processes taking place in the polyester matrix under the influence of γ 60Co radiation.

  6. Application of pyridinium salts derived of barbituric acid in Kröhnke's reaction.

    PubMed

    Prelicz, D; Kasperek, L

    1975-01-01

    A series of pyridinium salts derived of barbituric acid (BAC) was obtained, as starting substances in Kröhnke's reaction. On the example of 3-(1',3'-dimethyl-5'-isopropylbarbituryl-5')-1-acetonylene-N-pyrifinium bromide it was stated that the corresponding nitron can be formed only when in positions 1 and 3 of barbituric ring are no hydrogen atoms able to enolization. 3-(1',3'-Dimethyl-5'-isopropylbarbituryl-5')-pyruvic aldehyde (XIII) was obtained by decomposition of nitron XII. PMID:1144211

  7. Structural evidence for solvent-stabilisation by aspartic acid as a mechanism for halophilic protein stability in high salt concentrations.

    PubMed

    Lenton, Samuel; Walsh, Danielle L; Rhys, Natasha H; Soper, Alan K; Dougan, Lorna

    2016-07-21

    Halophilic organisms have adapted to survive in high salt environments, where mesophilic organisms would perish. One of the biggest challenges faced by halophilic proteins is the ability to maintain both the structure and function at molar concentrations of salt. A distinct adaptation of halophilic proteins, compared to mesophilic homologues, is the abundance of aspartic acid on the protein surface. Mutagenesis and crystallographic studies of halophilic proteins suggest an important role for solvent interactions with the surface aspartic acid residues. This interaction, between the regions of the acidic protein surface and the solvent, is thought to maintain a hydration layer around the protein at molar salt concentrations thereby allowing halophilic proteins to retain their functional state. Here we present neutron diffraction data of the monomeric zwitterionic form of aspartic acid solutions at physiological pH in 0.25 M and 2.5 M concentration of potassium chloride, to mimic mesophilic and halophilic-like environmental conditions. We have used isotopic substitution in combination with empirical potential structure refinement to extract atomic-scale information from the data. Our study provides structural insights that support the hypothesis that carboxyl groups on acidic residues bind water more tightly under high salt conditions, in support of the residue-ion interaction model of halophilic protein stabilisation. Furthermore our data show that in the presence of high salt the self-association between the zwitterionic form of aspartic acid molecules is reduced, suggesting a possible mechanism through which protein aggregation is prevented. PMID:27327567

  8. Chemically frozen multicomponent boundary layer theory of salt and/or ash deposition rates from combustion gases

    NASA Technical Reports Server (NTRS)

    Rosner, D. E.; Chen, B.-K.; Fryburg, G. C.; Kohl, F. J.

    1979-01-01

    There is increased interest in, and concern about, deposition and corrosion phenomena in combustion systems containing inorganic condensible vapors and particles (salts, ash). To meet the need for a computationally tractable deposition rate theory general enough to embrace multielement/component situations of current and future gas turbine and magnetogasdynamic interest, a multicomponent chemically 'frozen' boundary layer (CFBL) deposition theory is presented and its applicability to the special case of Na2SO4 deposition from seeded laboratory burner combustion products is demonstrated. The coupled effects of Fick (concentration) diffusion and Soret (thermal) diffusion are included, along with explicit corrections for effects of variable properties and free stream turbulence. The present formulation is sufficiently general to include the transport of particles provided they are small enough to be formally treated as heavy molecules. Quantitative criteria developed to delineate the domain of validity of CFBL-rate theory suggest considerable practical promise for the present framework, which is characterized by relatively modest demands for new input information and computer time.

  9. Safety evaluation of chitosan and chitosan acid salts from Panurilus argus lobster.

    PubMed

    Lagarto, Alicia; Merino, Nelson; Valdes, Odalys; Dominguez, Jesus; Spencer, Evelyn; de la Paz, Nilia; Aparicio, Guillermo

    2015-01-01

    Chitosan is a natural polymer with excellent properties such as biocompatibility, biodegradability, non-toxicity and adsorptive abilities. We obtained chitosan derived from Panurilus argus lobster shell and its lactate and acetate salts to introduce in pharmaceutical industry. We examined the single and repeated dose toxicity of chitosan and its lactate and acetate salts. Single oral doses of 2000 mg/kg were well tolerated for all three materials. In the repeat dose tests, animals treated with chitosan only show a slight erythrocytes increase. Variations in erythrocyte and leukocyte count and some biochemical parameters were observed in animals treated with chitosan acid salts. One g/kg orally was found to be the subacute NOAEL for chitosan due to the hematological findings observed were not considered adverse. Chitosans obtained from Panurilus argus lobster shell have low toxicity and may be safe in rats because it did not cause any lethality or changes in the general behavior in both the single and repeated dose toxicity studies. PMID:25450835

  10. Adsorption and condensation of amino acids and nucleotides with soluble mineral salts

    NASA Technical Reports Server (NTRS)

    Orenberg, J.; Lahav, N.

    1986-01-01

    The directed synthesis of biopolymers in an abiotic environment is presumably a cyclic sequence of steps which may be realized in a fluctuating environment such as a prebiotic pond undergoing wetting-drying cycles. Soluble mineral salts have been proposed as an essential component of this fluctuating environment. The following sequence may be considered as a most primitive mechanism of information transfer in a fluctuating environment: (1) adsorption of a biomolecule onto a soluable mineral salt surface to act as an adsorbed template; (2) specific adsorption of biomonomers onto the adsorbed template; (3) condensation of the adsorbed biomonomers; and (4) desorption of the elongated oligomer. In this investigation, the salts selected for study were CaSO4.2H2O(gypsum), SrSO4, and several other metal sulfates and chlorides. Adsorption of the monomeric species, gly, 5'AMP 5'GMP, and 5'CMP was investigated. The adsorbed template biopolymers used were Poly-A, Poly-G, Poly-C, and Poly-U. The results of studies involving these experimental participants, the first two steps of the proposed primitive information transfer mechanism, and condensation of amino acids to form oligomers in a fluctuating environment are to be reported.

  11. The influence of a small amount of maleic acid on crystal deposition phenomena of methacrylic acid in melt crystallization

    NASA Astrophysics Data System (ADS)

    Hino, Tomomichi; Kato, Shinpei; Takiyama, Hiroshi

    2013-06-01

    Crystal deposition phenomena were investigated in the suspension melt crystallization of an organic acid. Methacrylic acid was used as the target substance, a certain amount of methanol was used as the solvent, and the effect of a small amount of maleic acid by-produced in methacrylic acid synthesis was focused on. Batch crystallizations were carried out on a laboratory scale using various concentrations of maleic acid. In the presence of maleic acid, a certain deviation from equilibrium of the pure binary system was observed in the final composition of mother liquor. Moreover, nevertheless the final temperature in the crystallizer was same, the amount of crystal deposition in the presence of maleic acid was smaller than in the absence of maleic acid. It was suggested that the final amount of crystal deposition decreased in the presence of maleic acid. Additionally, it was observed that the obtained crystal size was smaller in the presence of maleic acid. Hence, a simplified kinetic analysis of crystal deposition rates was carried out to make the effect of maleic acid clear. Consequently, it was suggested that the cause of the above-mentioned phenomena was the existence of the maleic acid concentration dependent pseudo-liquidus line.

  12. 40 CFR 721.3130 - Sulfuric acid, mono-C9-11-alkyl esters, sodium salts.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Sulfuric acid, mono-C9-11-alkyl esters... Specific Chemical Substances § 721.3130 Sulfuric acid, mono-C9-11-alkyl esters, sodium salts. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as...

  13. 40 CFR 721.3130 - Sulfuric acid, mono-C9-11-alkyl esters, sodium salts.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Sulfuric acid, mono-C9-11-alkyl esters... Specific Chemical Substances § 721.3130 Sulfuric acid, mono-C9-11-alkyl esters, sodium salts. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as...

  14. 40 CFR 721.3130 - Sulfuric acid, mono-C9-11-alkyl esters, sodium salts.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Sulfuric acid, mono-C9-11-alkyl esters... Specific Chemical Substances § 721.3130 Sulfuric acid, mono-C9-11-alkyl esters, sodium salts. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as...

  15. 40 CFR 721.3130 - Sulfuric acid, mono-C9-11-alkyl esters, sodium salts.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Sulfuric acid, mono-C9-11-alkyl esters... Specific Chemical Substances § 721.3130 Sulfuric acid, mono-C9-11-alkyl esters, sodium salts. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as...

  16. 40 CFR 721.3130 - Sulfuric acid, mono-C9-11-alkyl esters, sodium salts.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Sulfuric acid, mono-C9-11-alkyl esters... Specific Chemical Substances § 721.3130 Sulfuric acid, mono-C9-11-alkyl esters, sodium salts. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as...

  17. Effect of pH alkaline salts of fatty acids on the inhibition of bacteria associated with poultry processing

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The agar diffusion assay was used to examine the effect of pH on the ability of alkaline salts of three fatty acids (FA) to inhibit growth of bacteria associated with poultry processing. FA solutions were prepared by dissolving 0.5 M concentrations of caprylic, capric, or lauric acid in separate ali...

  18. U.S. EPA WORKSHOP TO DEVELOP A SIMPLE MODEL FOR ACID DEPOSITION

    EPA Science Inventory

    The Acid Deposition Planning Staff in the Office of Acid Deposition/EPA requested that the Atmospheric Sciences Research Laboratory undertake the development of a low-computational-demanding model suitable for educational use in understanding the linear or non-linear nature of th...

  19. PROTOTYPE CONCENTRATION MONITOR FOR ESTIMATING ACIDIC DRY DEPOSITION

    EPA Science Inventory

    Dry deposition contributes significantly to the acidification of the ecosystem. However, difficulties in measuring dry deposition of reactive gases and fine particles make routine direct monitoring impractical. An alternate approach is to use the 'concentration monitoring' method...

  20. Acid deposition and air quality related values in north central Colorado wilderness areas. Final report

    SciTech Connect

    Hidy, G.M.

    1995-05-01

    Terrestrial and aquatic ecosystem response to atmospheric acid, sulfur, and nitrate deposition has been studied only in a very limited way in Colorado wilderness areas. However, the observed deposition rates in north central Colorado remain low relative to affected areas in the eastern United States and well within a range where no adverse ecological effects are expected. This report presents a survey of scientific information describing acid deposition and air quality related values, which may have implications for utility plant operations.

  1. Influence of neutral salts on the hydrothermal stability of acid-soluble collagen.

    PubMed

    Brown, E M; Farrell, H M; Wildermuth, R J

    2000-02-01

    The thermal stability of acid-soluble collagens was studied by circular dichroism (CD) spectroscopy. Adult bovine dermal collagen (BDC), rat-tail tendon collagen (RTC), and calf skin collagen (CSC) were compared. Despite some variability in amino acid composition and apparent molecular weight, the CD spectra for helical and unordered collagen structures were essentially the same for all the sources. The melting of these collagens occurs as a two-stage process characterized by a pretransition (Tp) followed by complete denaturation (Td). The characteristic temperatures vary with the source of the collagen; for mature collagens (BDC, RTC) Tp = 30 degrees C and Td = 36 degrees C, and for CSC Tp = 34 degrees C and Td = 40 degrees C. Neutral salts, NaCl or KCl, at low concentrations (0.02-0.2 M) appear to bind to the collagens and shift the thermal transitions of these collagens to lower temperatures. PMID:10945432

  2. A Locked Nucleic Acid Probe Based on Selective Salt-Induced Effect Detects Single Nucleotide Polymorphisms

    PubMed Central

    Zhang, Jing; Wu, Huizhe; Chen, Qiuchen; Zhao, Pengfei; Zhao, Haishan; Yao, Weifan; Wei, Minjie

    2015-01-01

    Detection of single based genetic mutation by using oligonucleotide probes is one of the common methods of detecting single nucleotide polymorphisms at known loci. In this paper, we demonstrated a hybridization system which included a buffer solution that produced selective salt-induced effect and a locked nucleic acid modified 12 nt oligonucleotide probe. The hybridization system is suitable for hybridization under room temperature. By using magnetic nanoparticles as carriers for PCR products, the SNPs (MDR1 C3435T/A) from 45 volunteers were analyzed, and the results were consistent with the results from pyrophosphoric acid sequencing. The method presented in this paper differs from the traditional method of using molecular beacons to detect SNPs in that it is suitable for research institutions lacking real-time quantitative PCR detecting systems, to detect PCR products at room temperature. PMID:26347880

  3. Preparation of volatile fatty acid (VFA) calcium salts by anaerobic digestion of glucose.

    PubMed

    Li, Xiaofen; Swan, Janis E; Nair, Giridhar R; Langdon, Alan G

    2015-01-01

    Many potentially useful intermediates such as hydrogen and volatile fatty acids (VFAs) are formed during the complex anaerobic digestion processes that produce methane from biomass. This study recovers VFAs from an anaerobic digester by a combination of gas stripping and absorption with calcium carbonate slurry. Glucose was used as the model substrate because it is readily available, inexpensive, and easily digested. Sludge from a meatworks anaerobic digester produced methane and carbon dioxide (and sometimes a small amount of hydrogen) when batch-fed with glucose. Conditioning the neutral anaerobic sludge to an acidic pH (below 4.8) was achieved using repeated 1 g L(-1) doses of glucose. After conditioning, mainly VFAs and hydrogen were produced. The intermediate VFAs could be stripped using headspace gas. In subsequent fed-batch digestion/stripping cycles, the pH decreased when glucose was added and then increased when the VFA was gas stripped. The predominant acids formed at low pH values were lactic, butyric, and acetic acids. Lactic acid was converted to VFAs during stripping. The VFA calcium salts recovered were 80% butyrate and 20% acetate with minor quantities of propionate and valerate. PMID:25274086

  4. The Effect of Salts on Electrospray Ionization of Amino Acids in the Negative Mode

    NASA Technical Reports Server (NTRS)

    Kim, H. I.; Johnson, P. V.; Beegle, L. W.; Kanik, I.

    2004-01-01

    The continued search for organics on Mars will require the development of simplified procedures for handling and processing of soil or rock core samples prior to analysis by onboard instrumentation. Extraction of certain organic molecules such as amino acids from rock and soil samples using a liquid solvent (H2O) has been shown to be more efficient (by approximately an order of magnitude) than heat extraction methods. As such, liquid extraction (using H2O) of amino acid molecules from rock cores or regolith material is a prime candidate for the required processing. In this scenario, electrospray ionization (ESI) of the liquid extract would be a natural choice for ionization of the analyte prior to interrogation by one of a variety of potential analytical separation techniques (mass spectroscopy, ion mobility spectroscopy, etc.). Aside from the obvious compatibility of ESI and liquid samples, ESI offers simplicity and a soft ionization capability. In order to demonstrate that liquid extraction and ESI can work as part of an in situ instrument on Mars, we must better understand and quantify the effect salts have on the ESI process. In the current work, we have endeavored to investigate the feasibility and limitations of negative mode ESI of Martian surface samples in the context of sample salt content using ion mobility spectroscopy (IMS).

  5. IUPAC-NIST Solubility Data Series. 90. Hydroxybenzoic Acid Derivatives in Binary and Ternary Systems. Part II. Hydroxybenzoic Acids, Hydroxybenzoates, and Hydroxybenzoic Acid Salts in Nonaqueous Systems

    NASA Astrophysics Data System (ADS)

    Goto, Ayako; Miyamoto, Hiroshi; Salomon, Mark; Goto, Rensuke; Fukuda, Hiroshi; Königsberger, Erich; Königsberger, Lan-Chi; Scharlin, Pirketta

    2011-06-01

    The solid-liquid solubility data for well defined nonaqueous binary and ternary systems are reviewed. One component includes hydroxybenzoic acid, hydroxybenzoate, and hydroxybenzoic acid salt, and another component includes a variety of organic compounds (hydrocarbons, alcohols, halogenated hydrocarbons, carboxylic acids, esters, et al.) and carbon dioxide. The ternary systems include mixtures of organic substances of various classes and carbon dioxide. The total number of compilation sheets is 270 for six types of system. Almost all data are expressed as mass percent and mole fraction as well as the originally reported units, while some data are expressed as molar concentration. Critical evaluation was carried out for the binary nonaqueous systems of 2-, 3-, and 4-hydroxybenzoic acids and hydroxybenzoates (methylparaben, ethylparaben, propylparaben, and butylparaben) in alcohols, 1-heptane, and benzene.

  6. 40 CFR 721.1550 - Benzenediazonium, 4-(di-methyl-amino)-, salt with 2-hy-droxy-5-sul-fo-benzoic acid (1:1).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...-amino)-, salt with 2-hy-droxy-5-sul-fo-benzoic acid (1:1). (a) Chemical substance and significant new...)-, salt with 2-hy-droxy-5-sul-fo-benzoic acid (1:1). 721.1550 Section 721.1550 Protection of Environment...)-, salt with 2-hydroxy-5-sulfobenzoic acid (1:1) (CAS No. 124737-31-1) (P-90-1366) is subject to......

  7. 40 CFR 721.1550 - Benzenediazonium, 4-(di-methyl-amino)-, salt with 2-hy-droxy-5-sul-fo-benzoic acid (1:1).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...-amino)-, salt with 2-hy-droxy-5-sul-fo-benzoic acid (1:1). (a) Chemical substance and significant new...)-, salt with 2-hy-droxy-5-sul-fo-benzoic acid (1:1). 721.1550 Section 721.1550 Protection of Environment...)-, salt with 2-hydroxy-5-sulfobenzoic acid (1:1) (CAS No. 124737-31-1) (P-90-1366) is subject to......

  8. Acidic Cs{sup +}, NH{sub 4}{sup +}, and K{sup +} salts of 12-tungstophosphoric acid as solid catalysts for isobutane/2-butene alkylation

    SciTech Connect

    Corma, A.; Martinez, A.; Martinez, C.

    1996-12-01

    The cesium, ammonium, and potassium salts of 12-tungstophosphoric acid (HPW) have been prepared with different stoichiometries (1{le}x{le}3) and their catalytic behavior measured for the liquid phase alkylation of isobutane with 2-butene at 80{degrees}C. The salts with a cation content of 2.5 {le}x{le}3, and that of Cs{sup +} with x=2, showed a much higher surface area than the parent acid, which is partially due to the formation of micropores. The micropores presented a fairly homogeneous distribution, with an average diameter in the range of 6-11 {Angstrom}, depending on the type of cation and cation content. The activity of the heteropoly acid and their monovalent type B salts for isobutane alkylation could be correlated with the surface acidity of the solids. Thus, the initial (1 min TOS) olefin conversion went through a maximum for the NH{sub 4}{sup +} and K{sup +} salts with a cation content of x = 2.5, and in the range of 2{le}x{le}2.5 in the case of the Cs{sup +} compounds. (NH{sub 4}){sup 2.5}PW showed a very high initial cracking activity (ca. 72 wt% C{sub 5}-C{sub 7} in C{sub 5+}), suggesting the presence of surface acid sites of a higher acid strength in the ammonium salt, as compared to the caesium and potassium salts with similar composition. In all cases the desired trimethylpentanes (TMPs) were the predominant compounds in the C{sub 8} fraction formed in the initial reaction stages. The deactivation rate also depended on the nature of the cation exchanged in the heteropoly salts. 57 refs., 7 figs., 4 tabs.

  9. Sensitivity of modeled atmospheric nitrogen species and nitrogen deposition to variations in sea salt emissions in the North Sea and Baltic Sea regions

    NASA Astrophysics Data System (ADS)

    Neumann, Daniel; Matthias, Volker; Bieser, Johannes; Aulinger, Armin; Quante, Markus

    2016-03-01

    Coarse sea salt particles are emitted ubiquitously from the ocean surface by wave-breaking and bubble-bursting processes. These particles impact the atmospheric chemistry by affecting the condensation of gas-phase species and, thus, indirectly the nucleation of new fine particles, particularly in regions with significant air pollution. In this study, atmospheric particle concentrations are modeled for the North Sea and Baltic Sea regions in northwestern Europe using the Community Multiscale Air Quality (CMAQ) modeling system and are compared to European Monitoring and Evaluation Programme (EMEP) measurement data. The sea salt emission module is extended by a salinity-dependent scaling of the sea salt emissions because the salinity in large parts of the Baltic Sea is very low, which leads to considerably lower sea salt mass emissions compared to other oceanic regions. The resulting improvement in predicted sea salt concentrations is assessed. The contribution of surf zone emissions is considered separately. Additionally, the impacts of sea salt particles on atmospheric nitrate and ammonium concentrations and on nitrogen deposition are evaluated. The comparisons with observational data show that sea salt concentrations are commonly overestimated at coastal stations and partly underestimated farther inland. The introduced salinity scaling improves the predicted Baltic Sea sea salt concentrations considerably. The dates of measured peak concentrations are appropriately reproduced by the model. The impact of surf zone emissions is negligible in both seas. Nevertheless, they might be relevant because surf zone emissions were cut at an upper threshold in this study. Deactivating sea salt leads to minor increases in NH3 + NH4+ and HNO3 + NO3- and a decrease in NO3- concentrations. However, the overall effect on NH3 + NH4+ and HNO3 + NO3- concentrations is smaller than the deviation from the measurements. Nitrogen wet deposition is underestimated by the model at most

  10. Effects of acid deposition on terrestrial ecosystems and their rehabilitation strategies in China.

    PubMed

    Feng, Zong-wei; Miao, Hong; Zhang, Fu-zhu; Huang, Yi-zong

    2002-04-01

    South China has become the third largest region associated with acid deposition following Europe and North America, the area subject to damage by acid deposition increased from 1.75 million km2 in 1985 to 2.8 million km2 in 1993. Acid deposition has caused serious damage to ecosystem. Combined pollution of acid rain and SO2 showed the obvious multiple effects on crops. Vegetable was more sensitive to acid deposition than foodstuff crops. Annual economic loss of crops due to acid deposition damage in eleven provinces of south China was 4.26 billion RMB Yuan. Acid deposition caused serious damage to forest. Annual economic loss of wood volume was about 1.8 billion RMB Yuan and forest ecological benefit loss 16.2 billion in eleven provinces of south China. Acid deposition in south China was typical "sulfuric acid type". According to the thoughts of sustainable development, some strategies were brought forward as follows: (1) enhancing environmental management, specifying acid-controlling region, controlling and abating the total emission amount of SO2; (2) selecting practical energy technologies of clean coal, for example, cleansing and selecting coal, sulfur-fixed-type industrial briqutting, abating sulfur from waste gas and so on; (3) developing other energy sources to replace coal, including water electricity, atomic energy and the new energy such as solar energy, wind energy and so on; (4) in acid deposition region of south China, selecting acid-resistant type of crop and tree to decrease agricultural losses, planting more green fertilizer crops, using organic fertilizers and liming, in order to improve buffer capacities of soil. PMID:12046292

  11. Atmospheric salt deposition in a tropical mountain rain forest at the eastern Andean slopes of South Ecuador - Pacific or Atlantic origin?

    NASA Astrophysics Data System (ADS)

    Makowski Giannoni, S.; Trachte, K.; Rollenbeck, R.; Lehnert, L.; Fuchs, J.; Bendix, J.

    2015-10-01

    Salt (NaCl) is recently proven to be of highest importance for ecosystem functioning of the Amazon lowland forests because of its importance for herbivory, litter decomposition and thus, carbon cycling. Salt deposition should generally decline with distance from its marine sources. For tropical South America, a negative east-west salt availability gradient is assumed in the Amazon as a consequence of the barrier effect of the Andes for Pacific air masses. However, this generalized pattern may not hold for the tropical mountain rain forest in the Andes of southern Ecuador. To analyze salt availability, we investigate the deposition of Na+ and Cl- which are good proxies of sea spray aerosol. Because of the complexity of the terrain and related cloud and rain formation processes, salt deposition was analyzed from both, rain and occult precipitation (OP) water along an altitudinal gradient over a period from 2004 to 2009. To assess the influence of Atlantic and Pacific air masses on the locally observed deposition of sodium and chloride, sea-salt aerosol concentration data from the Monitoring Atmospheric Composition and Climate (MACC) reanalysis dataset and back-trajectory statistical methods were combined. Our results based on deposition time series and 2192 generated trajectories show a clear difference in the temporal variation of sodium and chloride concentration due to height and exposure to winds. The sea-salt transport was highly seasonal where higher locations revealed a stronger seasonality. Although the influence of the easterlies were predominant regarding atmospheric circulation, the statistical analysis of trajectories and hybrid receptor models revealed a stronger impact of the Pacific sea-salt sources on the deposition at the study area. The highest concentration in rain and cloud water was found between September and February originating from both, the equatorial Pacific and Atlantic. However, the Pacific sources contributed with up to 25 % to the

  12. Effects of long-term grazing on sediment deposition and salt-marsh accretion rates

    NASA Astrophysics Data System (ADS)

    Elschot, Kelly; Bouma, Tjeerd J.; Temmerman, Stijn; Bakker, Jan P.

    2013-11-01

    Many studies have attempted to predict whether coastal marshes will be able to keep up with future acceleration of sea-level rise by estimating marsh accretion rates. However, there are few studies focussing on the long-term effects of herbivores on vegetation structure and subsequent effects on marsh accretion. Deposition of fine-grained, mineral sediment during tidal inundations, together with organic matter accumulation from the local vegetation, positively affects accretion rates of marsh surfaces. Tall vegetation can enhance sediment deposition by reducing current flow and wave action. Herbivores shorten vegetation height and this could potentially reduce sediment deposition. This study estimated the effects of herbivores on 1) vegetation height, 2) sediment deposition and 3) resulting marsh accretion after long-term (at least 16 years) herbivore exclusion of both small (i.e. hare and goose) and large grazers (i.e. cattle) for marshes of different ages. Our results firstly showed that both small and large herbivores can have a major impact on vegetation height. Secondly, grazing processes did not affect sediment deposition. Finally, trampling by large grazers affected marsh accretion rates by compacting the soil. In many European marshes, grazing is used as a tool in nature management as well as for agricultural purposes. Thus, we propose that soil compaction by large grazers should be taken in account when estimating the ability of coastal systems to cope with an accelerating sea-level rise.

  13. ACID PRECIPITATION IN NORTH AMERICA: 1987 ANNUAL AND SEASONAL DATA SUMMARIES FROM ACID DEPOSITION SYSTEM DATA BASE

    EPA Science Inventory

    This report summarizes the 1987 wet deposition precipitation chemistry data collected in North America and available in the Acid Deposition System (ADS) data base. nterpretative statistical analyses are not a focus of this report; however, users of the report will learn about maj...

  14. ACID PRECIPITATION IN NORTH AMERICA: 1980, 1981 AND 1982 ANNUAL DATA SUMMARIES FROM ACID DEPOSITION SYSTEM DATA BASE

    EPA Science Inventory

    The Acid Deposition System (ADS) data base for North American wet deposition data is used to provide an overview of the major North American monitoring networks: NADP, CANSAP, APN, MAP3S/PCN, EPRI/SURE, UAPSP and APIOS daily and cumulative. Individual site annual statistical summ...

  15. Expression of fatty acid desaturase genes and fatty acid accumulation in Chlamydomonas sp. ICE-L under salt stress.

    PubMed

    An, Meiling; Mou, Shanli; Zhang, Xiaowen; Zheng, Zhou; Ye, Naihao; Wang, Dongsheng; Zhang, Wei; Miao, Jinlai

    2013-12-01

    The Antarctic ice microalgae Chlamydomonas sp. ICE-L which is highly resistant to salt stress holds promise in providing an alternative species for the production of microalgal oil. We studied the effects of the alga in confrontation with NaCl stress on the growth, oil yield and expression of fatty acid desaturase genes. The growth rate of Chlamydomonas sp. ICE-L decreased with the gradual increase in NaCl concentration. Interestingly, we found that the highest lipid content was achieved at 16‰ NaCl, reaching 23% (w/w). Meanwhile, the expression of Δ9ACPCiFAD increased rapidly while Δ12CiFAD, ω3CiFAD2 and Δ6CiFAD showed a delayed elevation in response to altered salt stress. C18:3 was the dominant PUFA, which account for about 75% TFA in Chlamydomonas sp. ICE-L. Under 96‰ and 128‰ NaCl stress, the content of C20:5 almost approached that of C18:3. In contrast, low salinity enhanced the dominance of C18:3 at the expense of C20:3 and C20:5. PMID:24084208

  16. Separation of aromatic carboxylic acids using quaternary ammonium salts on reversed-phase HPLC. 1. Separation behavior of aromatic carboxylic acids

    SciTech Connect

    Kawamura, K.; Okuwaki, A.; Verheyen, T.; Perry, G.J.

    2006-02-15

    In order to develop separation processes and analytical methods for aromatic carboxylic acids for the coal oxidation products, the separation behavior of aromatic carboxylic acids on a reversed-phase HPLC using eluent containing quaternary ammonium salt has been investigated. The retention mechanism of aromatic carboxylic acids was discussed on the basis of both ion-pair partition model and ion-exchange model. The retention behavior of aromatic carboxylic acids possessing one (or two) carboxylic acid group(s) followed the ion-pair partition model, where linear free energy relationship was observed between the capacity factor and the extraction equilibrium constants of benzoic acid and naphthalene carboxylic acid. Besides, the retention behavior followed ion-exchange model with increasing the number of carboxylic acids, where the capacity factor of benzene polycarboxylic acids is proportional to the association constants between aromatic acids and quaternary ammonium ions calculated on the basis of an electrostatic interaction model.

  17. Iodine-Catalyzed Decarboxylative Amidation of β,γ-Unsaturated Carboxylic Acids with Chloramine Salts Leading to Allylic Amides.

    PubMed

    Kiyokawa, Kensuke; Kojima, Takumi; Hishikawa, Yusuke; Minakata, Satoshi

    2015-10-26

    The iodine-catalyzed decarboxylative amidation of β,γ-unsaturated carboxylic acids with chloramine salts is described. This method enables the regioselective synthesis of allylic amides from various types of β,γ-unsaturated carboxylic acids containing substituents at the α- and β-positions. In the reaction, N-iodo-N-chloroamides, generated by the reaction of a chloramine salt with I2 , function as a key active species. The reaction provides an attractive alternative to existing methods for the synthesis of useful secondary allylic amine derivatives. PMID:26493878

  18. Extraction of phenol using sulfuric acid salts of trioctylamine in a supported liquid membrane

    SciTech Connect

    Wang, M.L.; Hu, K.H. )

    1994-04-01

    The extraction of phenol by trioctylamine sulfate salts in a supported-liquid membrane (SLM) process was investigated. In the extraction process, a transport model, which included the film diffusion of phenol in the aqueous phase, the membrane diffusion within the SLM, and the interfacial chemical reaction, was built. The experimental parameters, such as the cell constant ([beta]), the diffusivity of (TOA)[sub 2]H[sub 2]SO[sub 4][center dot]PhOH in the SLM (D[sub c,b]), and the mass-transfer coefficient of phenol in the aqueous solution (K[sub L]), were determined from experiments. On the basis of the experimental data and the results obtained from the transport model, the rate-controlling step of the extraction of phenol by an SLM during permeation is discussed. The effects of the operating variables and parameters, such as the initial concentration of phenol in the aqueous phase, sulfuric acid, sodium hydroxide, and trioctylamine sulfate salts, on the extraction of phenol were examined.

  19. Localized corrosion of high performance metal alloys in an acid/salt environment

    NASA Technical Reports Server (NTRS)

    Macdowell, L. G.; Ontiveros, C.

    1991-01-01

    Various vacuum jacketed cryogenic supply lines at the Space Shuttle launch site at Kennedy Space Center use convoluted flexible expansion joints. The atmosphere at the launch site has a very high salt content, and during a launch, fuel combustion products include hydrochloric acid. This extremely corrosive environment has caused pitting corrosion failure in the thin walled 304L stainless steel flex hoses. A search was done to find a more corrosion resistant replacement material. The study focussed on 19 metal alloys. Tests which were performed include electrochemical corrosion testing, accelerated corrosion testing in a salt fog chamber, and long term exposure at a beach corrosion testing site. Based on the results of these tests, several nickel based alloys were found to have very high resistance to this corrosive environment. Also, there was excellent agreement between the electrochemical tests and the actual beach exposure tests. This suggests that electrochemical testing may be useful for narrowing the field of potential candidate alloys before subjecting samples to long term beach exposure.

  20. Extraction of metals and/or metalloids from acidic media using supercritical fluids and salts

    DOEpatents

    Wai, Chien M.; Smart, Neil G.; Lin, Yuehe

    1998-01-01

    A method of extracting metalloid and metal species from a solid or liquid material by exposing the material to a fluid solvent, particularly supercritical carbon dioxide, containing a chelating agent is described. The chelating agent forms chelates that are soluble in the fluid to allow removal of the species from the material. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent comprises a trialkyl phosphate, a triaryl phosphate, a trialkylphosphine oxide, a triarylphosphine oxide, or mixtures thereof. The method provides an environmentally benign process for removing contaminants from industrial waste. The method is particularly useful for extracting actinides from acidic solutions, and the process can be aided by the addition of nitrate salts. The chelate and supercritical fluid can be regenerated, and the contaminant species recovered, to provide an economic, efficient process.