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Sample records for barium sulfate precipitation

  1. Morphologies, mechanical properties and thermal stability of poly(lactic acid) toughened by precipitated barium sulfate

    NASA Astrophysics Data System (ADS)

    Yang, Jinian; Wang, Chuang; Shao, Kaiyun; Ding, Guoxin; Tao, Yulun; Zhu, Jinbo

    2015-11-01

    Poly(lactic acid) (PLA)-based composites were prepared by blending PLA with precipitated barium sulfate (BaSO4) modified with stearic acid. The morphologies, mechanical properties and thermal stability of samples with increased mass fraction of BaSO4 were investigated. Results showed that PLA was toughened and reinforced simultaneously by incorporation of precipitated BaSO4 particles. The highest impact toughness and elongation at break were both achieved at 15% BaSO4, while the elastic modulus increased monotonically with increasing BaSO4 loading. Little effect of BaSO4 on the thermal behavior of PLA was observed in the present case. However, the thermal stability of PLA/BaSO4 composites at high temperature was enhanced.

  2. Effects of nitrate and water on the oxygen isotopic analysis of barium sulfate precipitated from solution

    USGS Publications Warehouse

    Hannon, Janet E.; Bohlke, Johnkarl F.; Mroczkowski, Stanley J.

    2008-01-01

    BaSO4 precipitated from mixed salt solutions by common techniques for SO isotopic analysis may contain quantities of H2O and NOthat introduce errors in O isotope measurements. Experiments with synthetic solutions indicate that ?18O values of CO produced by decomposition of precipitated BaSO4 in a carbon reactor may be either too low or too high, depending on the relative concentrations of SO and NO and the ?18O values of the H2O, NO, and SO. Typical ?18O errors are of the order of 0.5 to 1‰ in many sample types, and can be larger in samples containing atmospheric NO, which can cause similar errors in ?17O and ?17O. These errors can be reduced by (1) ion chromatographic separation of SO from NO, (2) increasing the salinity of the solutions before precipitating BaSO4 to minimize incorporation of H2O, (3) heating BaSO4 under vacuum to remove H2O, (4) preparing isotopic reference materials as aqueous samples to mimic the conditions of the samples, and (5) adjusting measured ?18O values based on amounts and isotopic compositions of coexisting H2O and NO. These procedures are demonstrated for SO isotopic reference materials, synthetic solutions with isotopically known reagents, atmospheric deposition from Shenandoah National Park, Virginia, USA, and sulfate salt deposits from the Atacama Desert, Chile, and Mojave Desert, California, USA. These results have implications for the calibration and use of O isotope data in studies of SOsources and reaction mechanisms.

  3. Effects of nitrate and water on the oxygen isotopic analysis of barium sulfate precipitated from water samples.

    PubMed

    Hannon, Janet E; Böhlke, John Karl; Mroczkowski, Stanley J

    2008-12-01

    BaSO(4) precipitated from mixed salt solutions by common techniques for SO(4) (2-) isotopic analysis may contain quantities of H(2)O and NO(3) (-) that introduce errors in O isotope measurements. Experiments with synthetic solutions indicate that delta(18)O values of CO produced by decomposition of precipitated BaSO(4) in a carbon reactor may be either too low or too high, depending on the relative concentrations of SO(4) (2-) and NO(3) (-) and the delta(18)O values of the H(2)O, NO(3) (-), and SO(4) (2-). Typical delta(18)O errors are of the order of 0.5 to 1 per thousand in many sample types, and can be larger in samples containing atmospheric NO(3) (-), which can cause similar errors in delta(17)O and Delta(17)O. These errors can be reduced by (1) ion chromatographic separation of SO(4) (2-) from NO(3) (-), (2) increasing the salinity of the solutions before precipitating BaSO(4) to minimize incorporation of H(2)O, (3) heating BaSO(4) under vacuum to remove H(2)O, (4) preparing isotopic reference materials as aqueous samples to mimic the conditions of the samples, and (5) adjusting measured delta(18)O values based on amounts and isotopic compositions of coexisting H(2)O and NO(3) (-). These procedures are demonstrated for SO(4) (2-) isotopic reference materials, synthetic solutions with isotopically known reagents, atmospheric deposition from Shenandoah National Park, Virginia, USA, and sulfate salt deposits from the Atacama Desert, Chile, and Mojave Desert, California, USA. These results have implications for the calibration and use of O isotope data in studies of SO(4) (2-) sources and reaction mechanisms. PMID:19021238

  4. Effects of nitrate and water on the oxygen isotopic analysis of barium sulfate precipitated from water samples

    USGS Publications Warehouse

    Hannon, J.E.; Böhlke, J.K.; Mroczkowski, S.J.

    2008-01-01

    BaSO4 precipitated from mixed salt solutions by common techniques for SO42- isotopic analysis may contain quantities of H2O and NO3- that introduce errors in O isotope measurements. Experiments with synthetic solutions indicate that ??18O values of CO produced by decomposition of precipitated BaSO4 in a carbon reactor may be either too low or too high, depending on the relative concentrations of SO42- and NO3- and the ??18O values of the H2O, NO3-, and SO42-. Typical ??18O errors are of the order of 0.5 to 1??? in many sample types, and can be larger in samples containing atmospheric NO 3-, which can cause similar errors in ?? 17O and ??17O. These errors can be reduced by (1) ion chromatographic separation of SO42- from NO 3-, (2) increasing the salinity of the solutions before precipitating BaSO4 to minimize incorporation of H2O, (3) heating BaSO4 under vacuum to remove H2O, (4) preparing isotopic reference materials as aqueous samples to mimic the conditions of the samples, and (5) adjusting measured ??18O values based on amounts and isotopic compositions of coexisting H2O and NO 3-. These procedures are demonstrated for SO 42- isotopic reference materials, synthetic solutions with isotopically known reagents, atmospheric deposition from Shenandoah National Park, Virginia, USA, and sulfate salt deposits from the Atacama Desert, Chile, and Mojave Desert, California, USA. These results have implications for the calibration and use of O isotope data in studies of SO42- sources and reaction mechanisms.

  5. Co-precipitation of radium with barium and strontium sulfate and its impact on the fate of radium during treatment of produced water from unconventional gas extraction.

    PubMed

    Zhang, Tieyuan; Gregory, Kelvin; Hammack, Richard W; Vidic, Radisav D

    2014-04-15

    Radium occurs in flowback and produced waters from hydraulic fracturing for unconventional gas extraction along with high concentrations of barium and strontium and elevated salinity. Radium is often removed from this wastewater by co-precipitation with barium or other alkaline earth metals. The distribution equation for Ra in the precipitate is derived from the equilibrium of the lattice replacement reaction (inclusion) between the Ra(2+) ion and the carrier ions (e.g., Ba(2+) and Sr(2+)) in aqueous and solid phases and is often applied to describe the fate of radium in these systems. Although the theoretical distribution coefficient for Ra-SrSO4 (Kd = 237) is much larger than that for Ra-BaSO4 (Kd = 1.54), previous studies have focused on Ra-BaSO4 equilibrium. This study evaluates the equilibria and kinetics of co-precipitation reactions in Ra-Ba-SO4 and Ra-Sr-SO4 binary systems and the Ra-Ba-Sr-SO4 ternary system under varying ionic strength (IS) conditions that are representative of brines generated during unconventional gas extraction. Results show that radium removal generally follows the theoretical distribution law in binary systems and is enhanced in the Ra-Ba-SO4 system and restrained in the Ra-Sr-SO4 system by high IS. However, the experimental distribution coefficient (Kd') varies widely and cannot be accurately described by the distribution equation, which depends on IS, kinetics of carrier precipitation and does not account for radium removal by adsorption. Radium removal in the ternary system is controlled by the co-precipitation of Ra-Ba-SO4, which is attributed to the rapid BaSO4 nucleation rate and closer ionic radii of Ra(2+) with Ba(2+) than with Sr(2+). Carrier (i.e., barite) recycling during water treatment was shown to be effective in enhancing radium removal even after co-precipitation was completed. Calculations based on experimental results show that Ra levels in the precipitate generated in centralized waste treatment facilities far exceed regulatory limits for disposal in municipal sanitary landfills and require careful monitoring of allowed source term loading (ASTL) for technically enhanced naturally occurring materials (TENORM) in these landfills. Several alternatives for sustainable management of TENORM are discussed. PMID:24670034

  6. Radiation dose in mass screening for gastric cancer with high-concentration barium sulfate compared with moderate-concentration barium sulfate.

    PubMed

    Yamamoto, K; Azuma, M; Kuroda, C; Kubo, T; Yabunaka, K; Yamazaki, H; Katsuda, T; Takeda, Y

    2009-06-01

    Recently, high-concentration barium sulfate has been developed and is used in many medical facilities. This study compared radiation dose using high-concentration and moderate-concentration barium sulfate. The dose was evaluated with an experimental method using a gastric phantom and with a clinical examination. In the former, the dose and X-ray tube load were measured on the phantom with two concentrations of barium sulfate. In the latter, the fluoroscopic dose-area product (DAP), the radiographic DAP and their sum, the total DAP, were investigated in 150 subjects (112 males, 38 females) treated with both concentrations of barium sulfate. The effective dose was calculated by the software of PCXMC in every case. The results of the experimental evaluation indicated that the effective dose and X-ray tube load were greater with high-concentration barium sulfate than with moderate-concentration barium sulfate (p < 0.05). The results of the clinical evaluation indicated that the fluoroscopic DAP was greater with moderate-concentration barium sulfate than with high-concentration barium sulfate (p < 0.05), but the radiographic DAP was quite the reverse, so the total DAP and effective dose were almost same with both concentrations of barium sulfate. We conclude that high-concentration barium sulfate does not increase radiation dose in mass screening for gastric cancer. PMID:19623859

  7. Precipitation of calcium, magnesium, strontium and barium in tissues of four Acacia species (Leguminosae: Mimosoideae).

    PubMed

    He, Honghua; Bleby, Timothy M; Veneklaas, Erik J; Lambers, Hans; Kuo, John

    2012-01-01

    Precipitation of calcium in plants is common. There are abundant studies on the uptake and content of magnesium, strontium and barium, which have similar chemical properties to calcium, in comparison with those of calcium in plants, but studies on co-precipitation of these elements with calcium in plants are rare. In this study, we compared morphologies, distributional patterns, and elemental compositions of crystals in tissues of four Acacia species grown in the field as well as in the glasshouse. A comparison was also made of field-grown plants and glasshouse-grown plants, and of phyllodes of different ages for each species. Crystals of various morphologies and distributional patterns were observed in the four Acacia species studied. Magnesium, strontium and barium were precipitated together with calcium, mainly in phyllodes of the four Acacia species, and sometimes in branchlets and primary roots. These elements were most likely precipitated in forms of oxalate and sulfate in various tissues, including epidermis, mesophyll, parenchyma, sclerenchyma (fibre cells), pith, pith ray and cortex. In most cases, precipitation of calcium, magnesium, strontium and barium was biologically induced, and elements precipitated differed between soil types, plant species, and tissues within an individual plant; the precipitation was also related to tissue age. Formation of crystals containing these elements might play a role in regulating and detoxifying these elements in plants, and protecting the plants against herbivory. PMID:22848528

  8. Nickel hydroxide precipitation from aqueous sulfate media

    NASA Astrophysics Data System (ADS)

    Sist, Cinziana; Demopoulos, George P.

    2003-08-01

    Hydrometallurgical processing of laterite ores constitutes a major industrial and R&D activity in extractive metallurgy. In some of the process flowsheets, nickel hydroxide precipitation is incorporated. For these operations, the optimization of nickel hydroxide precipitation is important to assure efficiency and product quality. The main objective of this investigation was to study and improve the precipitation characteristics of Ni(OH)2 in a sulfate system using supersaturation controlled precipitation.

  9. Comparison of the reflectance characteristics of polytetrafluoroethylene and barium sulfate paints

    NASA Technical Reports Server (NTRS)

    Butner, C. L.; Schutt, J. B.; Shai, M. C.

    1984-01-01

    Preliminary results are presented of the directional reflectance measurements taken on two tetrafluorethylene (TFE) paints formulated with silicone binders. Both paints are found to be more Lambertian than barium sulfate paint and pressed powder, although the pigment to binder ratios for barium sulfate and TFE paints are about 133 and 3.3 to 1, respectively. The TFE paints exhibit total visible reflectances above 90 percent and offer surfaces that are not significantly affected by water.

  10. Development and Demonstration of a Sulfate Precipitation Process for Hanford Waste Tank 241-AN-107

    SciTech Connect

    SK Fiskum; DE Kurath; BM Rapko

    2000-08-16

    A series of precipitation experiments were conducted on Hanford waste tank 241-AN-107 samples in an effort to remove sulfate from the matrix. Calcium nitrate was added directly to AN-107 sub-samples to yield several combinations of Ca:CO{sub 3} mole ratios spanning a range of 0:1 to 3:1 to remove carbonate as insoluble CaCO{sub 3}. Similarly barium nitrate was added directly to the AN-107 aliquots, or to the calcium pretreated AN-107 aliquots, giving of Ba:SO{sub 4} mole ratios spanning a range of 1:1 to 5:1 to precipitate sulfate as BaSO{sub 4}. Initial bulk carbonate removal was required for successful follow-on barium sulfate precipitation. A {ge} 1:1 mole ratio of Ca:CO{sub 3} was found to lower the carbonate concentration such that Ba would react preferentially with the sulfate. A follow-on 1:1 mole ratio of Ba:SO{sub 4} resulted in 70% sulfate removal. The experiment was scaled up with a 735-mL aliquot of AN-107 for more complete testing. Calcium carbonate and barium sulfate settling rates were determined and fates of selected cations, anions, and radionuclides were followed through the various process steps. Seventy percent of the sulfate was removed in the scale-up test while recovering 63% of the filtrate volume. Surprisingly, during the scale-up test a sub-sample of the CaCO{sub 3}/241-AN-107 slurry was found to lose fluidity upon standing for {le} 2 days. Metathesis with BaCO{sub 3} at ambient temperature was also evaluated using batch contacts at various BaCO{sub 3}:SO{sub 4} mole ratios with no measurable success.

  11. Carboxylic acids: effective inhibitors for calcium sulfate precipitation?

    E-print Network

    Benning, Liane G.

    Carboxylic acids: effective inhibitors for calcium sulfate precipitation? TAHER RABIZADEH 1] ABSTRACT Results are reported here of an investigation into the effects of three carboxylic acid additives (tartaric, maleic and citric acids) on the precipitation of calcium sulfate phases. Precipitation reactions

  12. SOURCE ASSESSMENT: MAJOR BARIUM CHEMICALS

    EPA Science Inventory

    This report summarizes data on air emissions from the production of major barium chemicals. Compounds studied include barium sulfide, barium carbonate, barium chloride, barium hydroxide, and barium sulfate. In order to evaluate potential environmental effects the source severity,...

  13. Precipitation of LDL with sulfated polyanions: three methods compared.

    PubMed

    Siekmeier, R; März, W; Gross, W

    1988-10-31

    Three precipitation methods for the determination of low density lipoproteins have been evaluated. In n = 113 normolipidemic samples mean LDL-cholesterol levels have been 2.90 mmol/l, 2.77 mmol/l, 3.21 mmol/l after precipitation with heparin, dextran sulfate, and polyvinylsulfate, respectively. As compared to a combined ultracentrifugation and precipitation reference procedure (mean 3.22 mmol/l) two precipitation methods tend to underrate LDL-cholesterol. Elevated plasma triglycerides may interfere with the precipitation of LDL. The clinical relevance of the precipitation procedures has been studied by discriminant analysis in n = 28 consecutive patients admitted for coronary bypass operation and n = 28 controls. The data suggest that, statistically, the determination of LDL-cholesterol with either precipitation method only provides redundant information as in relation to the Friedewald approximation for LDL-cholesterol. Immunologically determined apolipoprotein B proved a better predictor for group separation than either precipitation method. PMID:2466586

  14. Reactions of calcium orthosilicate and barium zirconate with oxides and sulfates of various elements

    NASA Technical Reports Server (NTRS)

    Zaplatynsky, I.

    1979-01-01

    Calcium orthosilicate and barium zirconate were evaluated as the insulation layer of thermal barrier coatings for air cooled gas turbine components. Their reactions with various oxides and sulfates were studied at 1100 C and 1300 C for times ranging up to 400 and 200 hours, respectively. These oxides and sulfates represent potential impurities or additives in gas turbine fuels and in turbine combustion air, as well as elements of potential bond coat alloys. The phase compositions of the reaction products were determined by X-ray diffraction analysis. BaZrO3 and 2CaO-SiO2 both reacted with P2O5, V2O5, Cr2O3, Al2O3, and SiO2. In addition, 2CaO-SiO2 reacted with Na2O, BaO, MgO, and CoO and BaZrO3 reacted with Fe2O3.

  15. Precipitation of Barite by Myxococcus xanthus: Possible Implications for the Biogeochemical Cycle of Barium

    PubMed Central

    González-Muñoz, Maria Teresa; Fernández-Luque, Belén; Martínez-Ruiz, Francisca; Ben Chekroun, Kaoutar; Arias, José María; Rodríguez-Gallego, Manuel; Martínez-Cañamero, Magdalena; de Linares, Concepción; Paytan, Adina

    2003-01-01

    Bacterial precipitation of barite (BaSO4) under laboratory conditions is reported for the first time. The bacterium Myxococcus xanthus was cultivated in a solid medium with a diluted solution of barium chloride. Crystallization occurred as a result of the presence of live bacteria and the bacterial metabolic activity. A phosphorous-rich amorphous phase preceded the more crystalline barite formation. These experiments may indicate the involvement of bacteria in the barium biogeochemical cycle, which is closely related to the carbon cycle. PMID:12957970

  16. Barium Sulfate

    MedlinePLUS

    ... the mouth and stomach), stomach, and intestine using x-rays or computed tomography (CAT scan, CT scan; a ... scan that uses a computer to put together x-ray images to create cross-sectional or three dimensional ...

  17. Selective removal of keratan sulfate in chondroitin sulfate samples by sequential precipitation with ethanol.

    PubMed

    Galeotti, Fabio; Maccari, Francesca; Volpi, Nicola

    2014-03-01

    Keratan sulfate (KS) is present as a contaminant in chondroitin sulfate (CS) mainly extracted from shark cartilage. We report a selective removal procedure of KS in CS samples by means of sequential precipitation with ethanol. Purified shark CS containing approximately 10% to 15% KS was subjected to a precipitation procedure in the presence of increasing percentages of saturated ethanol. In contrast to other solvents, 1.0 volume of ethanol was able to selectively purify CS, with a purity of approximately 100%, from KS. The current selective and simple procedure appears to be a reliable industrial preparation of CS devoid of large amounts of the residual KS. PMID:24291704

  18. Precipitating Sodium Dodecyl Sulfate to Create Ultrastable and Stimulable Foams.

    PubMed

    Zhang, Li; Mikhailovskaya, Alesya; Yazhgur, Pavel; Muller, François; Cousin, Fabrice; Langevin, Dominique; Wang, Nan; Salonen, Anniina

    2015-08-10

    Ultrastable foams are made very simply by adding salt (NaCl or KCl) to sodium dodecyl sulfate. The addition of high concentrations of salt leads to the precipitation of the surfactant on the bubble surfaces and as crystals in the interstices between the bubbles. As a consequence, the ageing of the foams is stopped to make them stable indefinitely, or until they are heated above the melting temperature of the crystals. The use of KCl is shown to be much more effective than that of NaCl because potassium dodecyl sulfate has a higher melting temperature and faster rates of crystallization. The crystalline structures have been investigated inside the foam using small angle neutron scattering. The larger lattice spacing of the crystals formed with NaCl in comparison with KCl has been evidenced. These simple temperature stimulable foams could have many potential applications. PMID:26120060

  19. Quantitative Analysis of Sulfate in Water by Indirect EDTA Titration

    ERIC Educational Resources Information Center

    Belle-Oudry, Deirdre

    2008-01-01

    The determination of sulfate concentration in water by indirect EDTA titration is an instructive experiment that is easily implemented in an analytical chemistry laboratory course. A water sample is treated with excess barium chloride to precipitate sulfate ions as BaSO[subscript 4](s). The unprecipitated barium ions are then titrated with EDTA.…

  20. Sulfate-reducing bacteria release barium and radium from naturally occurring radioactive material in oil-field barite

    USGS Publications Warehouse

    Phillips, E.J.P.; Landa, E.R.; Kraemer, T.; Zielinski, R.

    2001-01-01

    Scale and sludge deposits formed during oil production can contain elevated levels of Ra, often coprecipitated with barium sulfate (barite). The potential for sulfate-reducing bacteria to release 226 Ra and Ba (a Ra analog) from oil-field barite was evaluated. The concentration of dissolved Ba increased when samples containing pipe scale, tank sludge, or oil-field brine pond sediment were incubated with sulfate-reducing bacteria Desulfovibrio sp., Str LZKI, isolated from an oil-field brine pond. However, Ba release was not stoichiometric with sulfide production in oil-field samples, and <0.1% of the Ba was released. Potential for the release of 226Ra was demonstrated, and the 226 Ra release associated with sulfate-reducing activity was predictable from the amount of Ba released. As with Ba, only a fraction of the 226Ra expected from the amount of sulfide produced was released, and most of the Ra remained associated with the solid material.

  1. Fabrication and surface properties of hydrophobic barium sulfate aggregates based on sodium cocoate modification

    NASA Astrophysics Data System (ADS)

    Hu, Linna; Wang, Guangxiu; Cao, Rong; Yang, Chun; Chen, Xi

    2014-10-01

    Hydrophobic barium sulfate aggregates were fabricated by the direction of cocoate anions. At 30 °C, when the weight ratio of sodium cocoate to BaSO4 particles was 2.0 wt.%, the active ratio of the product reached 99.43% and the contact angle was greater than 120°. This method could not only simplify the complex modification process, but reduce energy consumption. The surface morphology, chemical structure and composition of BaSO4 aggregates were characterized by SEM, XRD, and FTIR. The results indicated that the as-synthesized BaSO4 particles were almond-liked and were composed of many interconnected nanoballs and that their surfaces were affected by cocoate anions. The adsorption of cocoate anions reversed the charge and weakened the surface polarity of BaSO4 particles, driving the formation of aggregates. And cocoate anions induced a change of the BaSO4 particles surface from hydrophilic to hydrophobic by a self-assembly and transformation process. Due to the self-assembled structure and the surface hydrophobicity, when adding the hydrophobic BaSO4 into PVC, the mechanical properties of PVC composite materials were significantly improved.

  2. Precipitation method for barium metaborate (BaB2O4) synthesis from borax solution

    NASA Astrophysics Data System (ADS)

    Ak?ener, Eymen; Figen, Aysel Kantürk; Pi?kin, Sabriye

    2013-12-01

    In this study, barium metaborate (BaB2O4, BMB) synthesis from the borax solution was carried out. BMB currently is used in production of ceramic glazes, luminophors, oxide cathodes as well as additives to pigments for aqueous emulsion paints and also ?-BaB2O4 single crystals are the best candidate for fabrication of solid-state UV lasers operating at a wavelength of 200 nm due to excellent nonlinear optical properties. In the present study, synthesis was carried out from the borax solution (Na2B4O7?10H2O, BDH) and barium chloride (BaCI2?2H2O, Ba) in the glass-batch reactor with stirring. The effect of, times (5-15 min), molar ratio [stoich.ration (1.0:2.0), 1.25:2.0, 1.5:2.0, 2.5:2:0, 3.0:2.0, 3.5:2.0,4.0:2.0, 5.0:2.0] and also crystallization time (2-6 hour) on the BMB yield (%) was investigated at 80 °C reaction temperature. It is found that, BMB precipitation synthesis with 90 % yield can be performed from 0.50 molar ration (BDH:Ba), under 80 °C, 15 minute, and 6 hours crystallization time. The structural properties of BMB powders were characterized by using XRD, FT-IR and DTA-TG instrumental analysis technique.

  3. Nature and spatial distribution of sulfur species in a sulfated barium-based commercial lean NOx trap catalyst

    SciTech Connect

    Choi, Jae-Soon; Partridge Jr, William P; Lance, Michael J; Walker, Larry R; Pihl, Josh A; Toops, Todd J; FINNEY, Charles E A; Daw, C Stuart

    2010-01-01

    We report observations of the nature and spatial distribution of sulfur species on a sulfated Ba-based commercial lean NO{sub x} trap (LNT) catalyst. The monolithic catalyst was sulfated in a bench flow reactor during 60/4-s NO{sub x} storage/reduction cycling to achieve a total sulfur loading of 3.4 g L{sup -1} of catalyst. Washcoat composition, structure and sulfur distribution were analyzed with electron probe microanalysis, X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, and temperature-programmed reduction. The most significant washcoat elements of catalytic relevance were Pt, Pd, Rh, Ba, Ce, Zr, Mg, Al, and these were present mainly in four distinct domains; Mg/Al mixed oxide with Pt, Ce; Al oxide with Rh, Pd; Ce/Zr mixed oxide with Pt, Pd, Ba (high Ba content); Ce/Zr mixed oxide with Pt, Pd, Ba (lower Ba content). Sulfur was present in the form of sulfates that decreased in concentration along the LNT axis from front to back. Barium showed the highest sulfur affinity leading to a plug-like axial progression of its sulfation. The sulfation of AI, Mg/Al, and Ce/Zr oxides was less vigorous with a more axially dispersed and less penetrating front.

  4. Bioabsorbable bone fixation plates for X-ray imaging diagnosis by a radiopaque layer of barium sulfate and poly(lactic-co-glycolic acid).

    PubMed

    Choi, Sung Yoon; Hur, Woojune; Kim, Byeung Kyu; Shasteen, Catherine; Kim, Myung Hun; Choi, La Mee; Lee, Seung Ho; Park, Chun Gwon; Park, Min; Min, Hye Sook; Kim, Sukwha; Choi, Tae Hyun; Choy, Young Bin

    2015-04-01

    Bone fixation systems made of biodegradable polymers are radiolucent, making post-operative diagnosis with X-ray imaging a challenge. In this study, to allow X-ray visibility, we separately prepared a radiopaque layer and attached it to a bioabsorbable bone plate approved for clinical use (Inion, Finland). We employed barium sulfate as a radiopaque material due to the high X-ray attenuation coefficient of barium (2.196 cm(2) /g). The radiopaque layer was composed of a fine powder of barium sulfate bound to a biodegradable material, poly(lactic-co-glycolic acid) (PLGA), to allow layer degradation similar to the original Inion bone plate. In this study, we varied the mass ratio of barium sulfate and PLGA in the layer between 3:1 w/w and 10:1 w/w to modulate the degree and longevity of X-ray visibility. All radiopaque plates herein were visible via X-ray, both in vitro and in vivo, for up to 40 days. For all layer types, the radio-opacity decreased with time due to the swelling and degradation of PLGA, and the change in the layer shape was more apparent for layers with a higher PLGA content. The radiopaque plates released, at most, 0.5 mg of barium sulfate every 2 days in a simulated in vitro environment, which did not appear to affect the cytotoxicity. The radiopaque plates also exhibited good biocompatibility, similar to that of the Inion plate. Therefore, we concluded that the barium sulfate-based, biodegradable plate prepared in this work has the potential to be used as a fixation device with both X-ray visibility and biocompatibility. PMID:24964903

  5. BARIUM BIOAVAILABILITY AS THE CHLORIDE, SULFATE, OR CARBONATE SALT IN THE RAT

    EPA Science Inventory

    This study was conducted to determine how the bioavailability of a low concentration of barium (Ba) in drinking water is affected by anion speciation. Male Sprague Dawley rats weighing 250-300 grams were maintained on a diet of less than 1 mg Ba/kg of food for at least 1 month pr...

  6. The MSXX Force Field for the Barium Sulfate-Water Interface Yun Hee Jang,, Xiao Yan Chang, Mario Blanco, Sungu Hwang,, Yongchun Tang,

    E-print Network

    Goddard III, William A.

    , and CheVron Petroleum Technology Company, 2811 Hayes Road, Houston, Texas 77082 ReceiVed: September 5The MSXX Force Field for the Barium Sulfate-Water Interface Yun Hee Jang,, Xiao Yan Chang, Mario Simulation Center, Beckman Institute (139-74), California Institute of Technology, Pasadena, California 91125

  7. Co-precipitation of yttrium and barium fluorides from aqueous solutions

    SciTech Connect

    Fedorov, Pavel P.; Mayakova, Maria N.; Kuznetsov, Sergey V.; Voronov, Valery V.; Ermakov, Roman P.; Samarina, Kseniya S.; Popov, Arthur I.; Osiko, Vyacheslav V.

    2012-07-15

    Highlights: ? BaF{sub 2}–YF{sub 3} system has been studied under the non-equilibrium ambient conditions. ? Ba{sub 1?x}Y{sub x}F{sub 2+x} (x = 0.35–0.75) solid solution phase has cubic fluorite-type structure. ? Ba{sub 1?x}Y{sub x}F{sub 2+x} cubic crystal lattice parameter a{sub 0} does not change monotonously. ? Different types of lattice defects determine a dependency from sample composition. ? (H{sub 3}O{sup +})Y{sub 3}F{sub 10}{sup ?}·nH{sub 2}O phase precipitates from HF aqueous solutions instead of YF{sub 3}·nH{sub 2}O. -- Abstract: Co-precipitation of barium and yttrium fluorides from aqueous solutions at room temperature produced non-equilibrium Ba{sub 1?x}Y{sub x}F{sub 2+x} nanofluoride phase with face-centered cubic crystal lattice of fluorite-type with the composition interval of the homogeneity for x = 0.35–0.75. Lattice parameter a of this solid solution nanophase varied as a function of the sample chemical composition in a complex manner with two areas of linear dependency, from x = 0.35 to 0.45 and from x = 0.50 to 0.75. A plausible explanation of this phenomenon included a change of the type of crystal lattice defects and the manner of their population with the corresponding ions. An increase of the relative amount of yttrium in the HF reaction system led to the formation of hydroxonium salt of decafluorotriyttrium acid, (H{sub 3}O{sup +})Y{sub 3}F{sub 10}{sup ?}·nH{sub 2}O, instead of expected YF{sub 3} hydrate. No formation of oxyfluoride phases under acidic conditions has been observed.

  8. Effect of dispersant on preparation of barium-strontium titanate powders through oxalate co-precipitation method

    SciTech Connect

    Li Mingli Xu Mingxia

    2009-04-02

    The quantitative precipitation of barium-strontium titanyl oxalate: (Ba{sub 0.6}Sr{sub 0.4}TiO(C{sub 2}O{sub 4}){sub 2}.4H{sub 2}O, BSTO) precursor powders were successfully prepared through oxalate co-precipitation method. The pyrolysis of BSTO at 800 deg. C/4 h produced the barium-strontium titanate (Ba{sub 0.6}Sr{sub 0.4}TiO{sub 3}, BST) powders. Two kinds of dispersants namely ammonium salt of poly mathacrylic acid (PMAA-NH{sub 4}) and polyethylene glycol (PEG) were added respectively during the co-precipitation procedure. The powders were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM), etc. Experimental results show that the addition of the dispersants reduced the productive rate of BST powders. The BSTO and BST powders obtained by aforementioned technique without dispersants were homogeneous with quasi-orbicular morphology. The particles grew into spindle shape with the effect of PEG. The morphology homogeneity was broke with small grains as well as large agglomerated particles concurrent when PMAA-NH{sub 4} was added. The mechanism of the effect of the two dispersants was investigated in detail.

  9. Reduction and precipitation of neptunium(V) by sulfate-reducing bacteria.

    SciTech Connect

    Banaszak, J. E.; Rittmann, B. E.; Reed, D. T.

    1999-10-21

    Migration of neptunium, as NpO{sub 2}{sup +}, has been identified as a potentially important pathway for actinide release at nuclear waste repositories and existing sites of subsurface contamination. Reduction of Np(V) to Np(IV) will likely reduce its volubility, resulting in lowered subsurface migration. The ability of sulfate-reducing bacteria (SRB) to utilize Np(V) as an electron acceptor was investigated, because these bacteria are active in many anaerobic aquifers and are known to facilitate the reduction of metals and radionuclides. Pure and mixed cultures of SRB were able to precipitate neptunium during utilization of pyruvate, lactate, and hydrogen as electron donors in the presence and absence of sulfate. The neptunium in the precipitate was identified as Np(IV) using X-ray absorption near edge spectroscopy (XANES) analysis. In mixed-culture studies, the addition of hydrogen to consortia grown by pyruvate fermentation stimulated neptunium reduction and precipitation. Experiments with pure cultures of Desulfovibrio vulgaris, growing by lactate fermentation in the absence of sulfate or by sulfate reduction, confirm that the organism is active in neptunium reduction and precipitation. Based on our results, the activity of SRB in the subsurface may have a significant, and potentially beneficial, impact on actinide mobility by reducing neptunium volubility.

  10. Evaluation of Radiation Dose Reduction during CT Scans Using Oxide Bismuth and Nano-Barium Sulfate Shields

    E-print Network

    Seoung, Youl-Hun

    2015-01-01

    The purpose of the present study was to evaluate radiation dose reduction and image quality during CT scanning by using a new dose reduction fiber sheet (DRFS) with commercially available bismuth shields. These DRFS were composed of nano-barium sulfate (BaSO4), filling the gaps left by the large oxide bismuth (Bi2O3) particle sizes. The radiation dose was measured five times at directionss of 12 o'clock from the center of the polymethyl methacrylate (PMMA) head phantom to calculate an average value using a CT ionization chamber. The image quality measured CT transverse images of the PMMA head phantom depending on X-ray tube voltages and the type of shielding. Two regions of interest in CT transverse images were chosen from the right and left areas under the surface of the PMMA head phantom and from ion chamber holes located at directions of 12 o'clock from the center of the PMMA head phantom. The results of this study showed that the new DRFS shields could reduce dosages to 15.61%, 23.05%, and 22.71% more in ...

  11. Factors Affecting the Precipitation of Potassium Jarosite in Sulfate and Chloride Media

    NASA Astrophysics Data System (ADS)

    Dutrizac, J. E.

    2008-12-01

    The factors affecting the precipitation of potassium jarosite in both sulfate and chloride media were systematically investigated for the range of conditions likely to be encountered in hydrometallurgical practice. In sulfate solutions at 97 °C, the amount of precipitate increases with increasing retention times up to 10 hours, with increasing temperatures to approximately 100 °C, and with increasing ferric-ion concentrations. Despite the variations in the amount of precipitate, the composition remains nearly constant and is characteristic of that of potassium jarosite. The presence of potassium jarosite seed accelerates the rate of precipitation and results in near-maximum amounts of precipitate after just a few hours of reaction. The presence of ferrous sulfate has a negligible effect on both the product yield and composition. The amount of precipitate decreases with increasing acid concentrations, but the composition of the precipitates remains nearly constant, even for acid concentrations as high as 1.0 M H2SO4. Both the amount and composition of the precipitates vary as the K2SO4 concentration increases; in the presence of excess ferric ions, nearly complete K precipitation occurs. Small amounts of Cu2+, Zn2+, and Pb2+ are incorporated in the structure of potassium jarosite, and the amount increases with increasing concentrations of the divalent metal ions. Potassium jarosite is readily formed in chloride media at 140 °C, provided that an independent source of sulfate ions is available. A minimum K concentration is required in order to avoid the formation of hematite; at higher K concentrations, however, the product composition becomes nearly constant and reflects that of potassium jarosite. Both the product yield and composition are independent of the chloride concentration, added as LiCl, and the ferrous ion concentration, added as FeCl2. Although increasing concentrations of HCl result in a near-linear decrease in the amount of precipitate, the composition is independent of the HCl concentration and is characteristic of that of potassium jarosite. Increasing temperatures to 200 °C result in an increase in the product yield, but have no significant effect on the composition of the potassium jarosite precipitates.

  12. Evaluation of radiation dose reduction during CT scans by using bismuth oxide and nano-barium sulfate shields

    NASA Astrophysics Data System (ADS)

    Seoung, Youl-Hun

    2015-07-01

    The purpose of the present study was to evaluate the radiation dose reduction and the image quality during CT scanning by using a new dose reduction fiber sheet (DRFS) with commercially available bismuth shields. These DRFS, were composed of nano-barium sulfate (BaSO4) filling the gaps left by the large bismuth oxide (Bi2O3) particles. The radiation dose was measured five times at a direction of 12 o'clock from the center of the polymethyl methacrylate (PMMA) head phantom by using a CT ionization chamber to calculate an average value. The image quality of measured CT transverse images of the PMMA head phantom depended on the X-ray tube voltage and the type of shielding. Two regions of interest in the CT transverse images were chosen, one from the right area and the other from the left area under the surface of the PMMA head phantom and at a distance of ion chamber holes located in a direction of 12 o'clock from the center of the PMMA head phantom. The results of this study showed that the new DRFS shields could reduce the dosages by 15.61%, 23.05%, and 22.71% at 90 kVp, 120 kVp, and 140 kVp, respectively, than with these of a conventional bismuth shield of the same thickness while maintaining image quality. In addition, the DRFSs produced were about 25% thinness than conventional bismuth. We conclude, therefore, that a DRFS can replace conventional bismuth as a new shield.

  13. COMPARISON OF WET CHEMICAL AND INSTRUMENTAL METHODS FOR MEASURING AIRBORNE SULFATE

    EPA Science Inventory

    Four techniques for determination of water soluble sulfate in atmospheric samples were compared including the barium sulfate turbidimetric method, the Brosset (barium-Thorin) method, the automated barium-methylthymol blue procedure and a microchemical (barium-dinitro-sulfanazo II...

  14. Precipitation method for barium metaborate (BaB{sub 2}O{sub 4}) synthesis from borax solution

    SciTech Connect

    Ak?ener, Eymen; Figen, Aysel Kantürk; Pi?kin, Sabriye

    2013-12-16

    In this study, barium metaborate (BaB{sub 2}O{sub 4}, BMB) synthesis from the borax solution was carried out. BMB currently is used in production of ceramic glazes, luminophors, oxide cathodes as well as additives to pigments for aqueous emulsion paints and also ??BaB{sub 2}O{sub 4} single crystals are the best candidate for fabrication of solid-state UV lasers operating at a wavelength of 200 nm due to excellent nonlinear optical properties. In the present study, synthesis was carried out from the borax solution (Na{sub 2}B{sub 4}O{sub 7?}10H{sub 2}O, BDH) and barium chloride (BaCI{sub 2?}2H{sub 2}O, Ba) in the glass-batch reactor with stirring. The effect of, times (5-15 min), molar ratio [stoich.ration (1.0:2.0), 1.25:2.0, 1.5:2.0, 2.5:2:0, 3.0:2.0, 3.5:2.0,4.0:2.0, 5.0:2.0] and also crystallization time (2-6 hour) on the BMB yield (%) was investigated at 80 °C reaction temperature. It is found that, BMB precipitation synthesis with 90 % yield can be performed from 0.50 molar ration (BDH:Ba), under 80 °C, 15 minute, and 6 hours crystallization time. The structural properties of BMB powders were characterized by using XRD, FT-IR and DTA-TG instrumental analysis technique.

  15. Short-Range Dissolution-Precipitation Crystallization of Hydrothermal Barium Titanate

    SciTech Connect

    Qi, Lai; Lee, Burtrand I.; Badheka, Prerak; Yoon, Dang-Hyok; Samuels, William D.; Exarhos, Gregory J.

    2004-07-01

    A modified autoclave was used to investigate the crystallization mechanism of BaTiO3 during the hydrothermal reaction of Ba(OH)2 and TiO2 anatase. An uneven distribution of the crystallized BaTiO3 particles was observed: more than 99 wt% of total BaTiO3 articles remained where the precursor TiO2 was put; less than 1 wt% was collected from the areas away from the TiO2. According to the experimental observations in this work and proofs reported in the literature, we propose that the crystallization mechanism is dissolution-precipitation in nature, but the soluble Ti4+ species can only redisperse in a short distance away from TiO2 particles before precipitation. In another words, the nucleation of hydrothermal BaTiO3 starts at a low concentration of Ti4+. The mechanism of the Ba(OH)2-Ti(OH)4 reaction is a fast dehydration process.

  16. NMR chemical shift pattern changed by ammonium sulfate precipitation in cyanobacterial phytochrome Cph1

    PubMed Central

    Song, Chen; Lang, Christina; Kopycki, Jakub; Hughes, Jon; Matysik, Jörg

    2015-01-01

    Phytochromes are dimeric biliprotein photoreceptors exhibiting characteristic red/far-red photocycles. Full-length cyanobacterial phytochrome Cph1 from Synechocystis 6803 is soluble initially but tends to aggregate in a concentration-dependent manner, hampering attempts to solve the structure using NMR and crystallization methods. Otherwise, the Cph1 sensory module (Cph1?2), photochemically indistinguishable from the native protein and used extensively in structural and other studies, can be purified to homogeneity in >10 mg amounts at mM concentrations quite easily. Bulk precipitation of full-length Cph1 by ammonium sulfate (AmS) was expected to allow us to produce samples for solid-state magic-angle spinning (MAS) NMR from dilute solutions before significant aggregation began. It was not clear, however, what effects the process of partial dehydration might have on the molecular structure. Here we test this by running solid-state MAS NMR experiments on AmS-precipitated Cph1?2 in its red-absorbing Pr state carrying uniformly 13C/15N-labeled phycocyanobilin (PCB) chromophore. 2D 13C–13C correlation experiments allowed a complete assignment of 13C responses of the chromophore. Upon precipitation, 13C chemical shifts for most of PCB carbons move upfield, in which we found major changes for C4 and C6 atoms associated with the A-ring positioning. Further, the broad spectral lines seen in the AmS 13C spectrum reflect primarily the extensive inhomogeneous broadening presumably due to an increase in the distribution of conformational states in the protein, in which less free water is available to partake in the hydration shells. Our data suggest that the effect of dehydration process indeed leads to changes of electronic structure of the bilin chromophore and a decrease in its mobility within the binding pocket, but not restricted to the protein surface. The extent of the changes induced differs from the freezing process of the solution samples routinely used in previous MAS NMR and crystallographic studies. AmS precipitation might nevertheless provide useful protein structure/functional information for full-length Cph1 in cases where neither X-ray crystallography nor conventional NMR methods are available. PMID:26284254

  17. NMR chemical shift pattern changed by ammonium sulfate precipitation in cyanobacterial phytochrome Cph1.

    PubMed

    Song, Chen; Lang, Christina; Kopycki, Jakub; Hughes, Jon; Matysik, Jörg

    2015-01-01

    Phytochromes are dimeric biliprotein photoreceptors exhibiting characteristic red/far-red photocycles. Full-length cyanobacterial phytochrome Cph1 from Synechocystis 6803 is soluble initially but tends to aggregate in a concentration-dependent manner, hampering attempts to solve the structure using NMR and crystallization methods. Otherwise, the Cph1 sensory module (Cph1?2), photochemically indistinguishable from the native protein and used extensively in structural and other studies, can be purified to homogeneity in >10 mg amounts at mM concentrations quite easily. Bulk precipitation of full-length Cph1 by ammonium sulfate (AmS) was expected to allow us to produce samples for solid-state magic-angle spinning (MAS) NMR from dilute solutions before significant aggregation began. It was not clear, however, what effects the process of partial dehydration might have on the molecular structure. Here we test this by running solid-state MAS NMR experiments on AmS-precipitated Cph1?2 in its red-absorbing Pr state carrying uniformly (13)C/(15)N-labeled phycocyanobilin (PCB) chromophore. 2D (13)C-(13)C correlation experiments allowed a complete assignment of (13)C responses of the chromophore. Upon precipitation, (13)C chemical shifts for most of PCB carbons move upfield, in which we found major changes for C4 and C6 atoms associated with the A-ring positioning. Further, the broad spectral lines seen in the AmS (13)C spectrum reflect primarily the extensive inhomogeneous broadening presumably due to an increase in the distribution of conformational states in the protein, in which less free water is available to partake in the hydration shells. Our data suggest that the effect of dehydration process indeed leads to changes of electronic structure of the bilin chromophore and a decrease in its mobility within the binding pocket, but not restricted to the protein surface. The extent of the changes induced differs from the freezing process of the solution samples routinely used in previous MAS NMR and crystallographic studies. AmS precipitation might nevertheless provide useful protein structure/functional information for full-length Cph1 in cases where neither X-ray crystallography nor conventional NMR methods are available. PMID:26284254

  18. Influence of semi-batch operation on the precipitation of natrojarosite particles from sulfate solutions

    NASA Astrophysics Data System (ADS)

    Sandré, Anne-Laure; Gaunand, Alain

    2012-03-01

    The precipitation of natrojarosite from iron sodium sulfate solutions has been investigated at temperatures close to the atmospheric boiling point, in batch and semi-batch conditions. Semi-batch conditions make it possible to maintain a weaker iron concentration in the stirred reactor, leading to lower supersaturations, closer to those in continuous and possibly seeded MSMPRs or tanks—in series units. In these reactors, primary and secondary nucleations are few, allowing the growth of pure mono-crystalline particles of controlled size and size dispersion. Both modi operandi lead to agglomerates made of crystals of cubic habit. The surface of cauliflower-like particles from the batch modus operandi displays overlaying crystals, of size between 100 and 400 nm. The particles from the semi-batch mode, with moderate iron addition, are rougher and show bigger intergrown constitutive crystals of size up to a few microns, which denotes lesser secondary nucleation and more growth. A model is developed to characterize iron(III) and sulfate speciation with non-ideal behavior in the mother solution. It is used to compare the variations of supersaturation in the reactor between the batch and the semi-batch conditions. During the first 500 min, the supersaturation resulting from a moderate addition of iron is 10,000-10 times lower than during batch kinetics, which agrees with the reduction of secondary nucleation suggested by scanning electron micrographs. The semi-batch technique, which can be combined with the addition of support particles, is worth further work, aiming to reduce secondary nucleation and to determine the crystallite growth rate expression of natrojarosite as a function of supersaturation, using the model of solution developed in this work.

  19. Assessment of sulfate sources in high-elevation Asian precipitation using stable sulfur isotopes.

    PubMed

    Pruett, Lee E; Kreutz, Karl J; Wadleigh, Moire; Aizen, Vladimir

    2004-09-15

    Stable sulfur isotope measurements (delta34S) made on samples collected from a 2 m snowpit on the Inilchek Glacier, Tien Shan Mountains (42.16 degrees N, 80.25 degrees E, 5100 m) are used to estimate sources of sulfate (SO4(2-)) in high-elevation Central Asian precipitation. Comparison of snowpit oxygen isotope (delta18O) data with previous work constrains the age of the snowpit samples to the summer season during which they were retrieved (1999). Delta34S measurements were made at 10 cm resolution (20 samples total), with delta34S values ranging from 0.4/1000 during background ([SO4(2-)] < 1 microequiv L(-1)) periods to 19.4/1000 during a single high [SO4(2-)] event. On the basis of the significant correlation (r = 0.87) between [SO4(2-)] and delta34S values, coupled with major ion concentration time series and concentration ratios, we suggest a two-component mixing system consisting of evaporite dust and anthropogenic SO4(2-) to explain the observed delta34S values. Using a regression model, we estimate that during the 1999 summer season 60% of the deposited SO4(2-) was from an evaporite dust source, while 40% of the SO4(2-) was from anthropogenic sources. Due to the potentially large and unconstrained range of delta34S values for both evaporite and anthropogenic SO4(2-) sources in Asia, the error in our estimates is difficult to assess. However, the delta34S data from the 1999 Tien Shan snowpit provide the first unambiguous identification of evaporite and anthropogenic SO4(2-) in high-elevation Asian precipitation, and future ice core studies using improved analysis techniques and source delta34S values can provide detailed information on sulfur biogeochemistry and anthropogenic impacts in Asian alpine regions. PMID:15487779

  20. The role of non-precipitating clouds in producing ambient sulfate during summer: Results from simulations with the Acid Deposition and Oxidant Model (ADOM)

    NASA Astrophysics Data System (ADS)

    Karamchandani, Prakash; Venkatram, Akula

    A comprehensive acid deposition model was used to investigate the importance of non-precipitating stratus clouds for the production of ambient sulfate. A comparison of model estimates of ambient sulfate and SO 2 concentrations with corresponding observations for an episode in the summer of 1988 showed that the model underestimated ambient sulfate concentrations and overestimated ambient SO 2 concentrations when non-precipitating stratus clouds were ignored in the model formulation. When the model was modified to include non-precipitating stratus clouds, a distinct improvement in model performance was obtained.

  1. Biodegradation of BTEX and Other Petroleum Hydrocarbons by Enhanced and Controlled Sulfate Reduction

    SciTech Connect

    Song Jin

    2007-07-01

    High concentrations of sulfide in the groundwater at a field site near South Lovedale, OK, were inhibiting sulfate reducing bacteria (SRB) that are known to degrade contaminants including benzene, toluene, ethylbenzene, and m+p-xylenes (BTEX). Microcosms were established in the laboratory using groundwater and sediment collected from the field site and amended with various nutrient, substrate, and inhibitor treatments. All microcosms were initially amended with FeCl{sub 2} to induce FeS precipitation and, thereby, reduce sulfide concentrations. Complete removal of BTEX was observed within 39 days in treatments with various combinations of nutrient and substrate amendments. Results indicate that elevated concentration of sulfide is a limiting factor to BTEX biodegradation at this site, and that treating the groundwater with FeCl{sub 2} is an effective remedy to facilitate and enhance BTEX degradation by the indigenous SRB population. On another site in Moore, OK, studies were conducted to investigate barium in the groundwater. BTEX biodegradation by SRB is suspected to mobilize barium from its precipitants in groundwater. Data from microcosms demonstrated instantaneous precipitation of barium when sulfate was added; however, barium was detected redissolving for a short period and precipitating eventually, when active sulfate reduction was occurring and BTEX was degraded through the process. SEM elemental spectra of the evolved show that sulfur was not present, which may exclude BaSO{sub 4} and BaS as a possible precipitates. The XRD analysis suggests that barium probably ended in BaS complexing with other amorphous species. Results from this study suggest that SRB may be able to use the sulfate from barite (BaSO{sub 4}) as an electron acceptor, resulting in the release of free barium ions (Ba{sup 2+}), and re-precipitate it in BaS, which exposes more toxicity to human and ecological health.

  2. Modeling investigation of controlling factors in the increasing ratio of nitrate to non-seasalt sulfate in precipitation over Japan

    NASA Astrophysics Data System (ADS)

    Itahashi, Syuichi; Uno, Itsushi; Hayami, Hiroshi; Fujita, Shin-ichi

    2014-08-01

    Anthropogenic emissions in East Asia have been increasing during the three decades since 1980, as the population of East Asia has grown and the economies in East Asian countries have expanded. This has been particularly true in China, where NOx emissions have been rising continuously. However, because of fuel-gas desulfurization systems introduced as part of China’s 11th Five-Year Plan (2006-2010), SO2 emissions in China reached a peak in 2005-2006 and have declined since then. These drastic changes in emission levels of acidifying species are likely to have caused substantial changes in the precipitation chemistry. The absolute concentration of compounds in precipitation is inherently linked to precipitation amount; therefore, we use the ratio of nitrate (NO) to non-seasalt sulfate (nss-SO2-) concentration in precipitation as an index for evaluating acidification, which we call Ratio. In this study, we analyzed the long-term behavior of Ratio in precipitation over the Japanese archipelago during 2000-2011 and estimated the factors responsible for changes in Ratio in precipitation by using a model simulation. This analysis showed that Ratio was relatively constant at 0.5-0.6 between 2000 and 2005, and subsequently increased to 0.6-0.7 between 2006 and 2011. These changes in Ratio corresponded remarkably well to the changes of NOx/SO2 emissions ratio in China; this correspondence suggests that anthropogenic emissions from China were responsible for most of the change in precipitation chemistry over Japan. Sensitivity analysis elucidated that the increase in NOx emissions and the decrease in SO2 emissions contributed equally to the increases in Ratio. Considering both emission changes in China enables to capture the observed increasing trend of Ratio in Japan.

  3. BACKGROUND CONCENTRATION OF SULFATE IN PRECIPITATION ALONG WITH WEST COAST OF NORTH AMERICA

    EPA Science Inventory

    The pH is not sufficient to characterize the acidity of precipitation, but rather its acid-base components must be described. he chemistry of natural emission sources as well as the mechanisms of precipitation formation are key factors in determining the chemistry of precipitatio...

  4. Dissolution-precipitation processes in tank experiments for testing numerical models for reactive transport calculations: Experiments and modelling.

    PubMed

    Poonoosamy, Jenna; Kosakowski, Georg; Van Loon, Luc R; Mäder, Urs

    2015-01-01

    In the context of testing reactive transport codes and their underlying conceptual models, a simple 2D reactive transport experiment was developed. The aim was to use simple chemistry and design a reproducible and fast to conduct experiment, which is flexible enough to include several process couplings: advective-diffusive transport of solutes, effect of liquid phase density on advective transport, and kinetically controlled dissolution/precipitation reactions causing porosity changes. A small tank was filled with a reactive layer of strontium sulfate (SrSO4) of two different grain sizes, sandwiched between two layers of essentially non-reacting quartz sand (SiO2). A highly concentrated solution of barium chloride was injected to create an asymmetric flow field. Once the barium chloride reached the reactive layer, it forced the transformation of strontium sulfate into barium sulfate (BaSO4). Due to the higher molar volume of barium sulfate, its precipitation caused a decrease of porosity and lowered the permeability. Changes in the flow field were observed with help of dye tracer tests. The experiments were modelled using the reactive transport code OpenGeosys-GEM. Tests with non-reactive tracers performed prior to barium chloride injection, as well as the density-driven flow (due to the high concentration of barium chloride solution), could be well reproduced by the numerical model. To reproduce the mineral bulk transformation with time, two populations of strontium sulfate grains with different kinetic rates of dissolution were applied. However, a default porosity permeability relationship was unable to account for measured pressure changes. Post mortem analysis of the strontium sulfate reactive medium provided useful information on the chemical and structural changes occurring at the pore scale at the interface that were considered in our model to reproduce the pressure evolution with time. PMID:25805363

  5. Dissolution-precipitation processes in tank experiments for testing numerical models for reactive transport calculations: Experiments and modelling

    NASA Astrophysics Data System (ADS)

    Poonoosamy, Jenna; Kosakowski, Georg; Van Loon, Luc R.; Mäder, Urs

    2015-06-01

    In the context of testing reactive transport codes and their underlying conceptual models, a simple 2D reactive transport experiment was developed. The aim was to use simple chemistry and design a reproducible and fast to conduct experiment, which is flexible enough to include several process couplings: advective-diffusive transport of solutes, effect of liquid phase density on advective transport, and kinetically controlled dissolution/precipitation reactions causing porosity changes. A small tank was filled with a reactive layer of strontium sulfate (SrSO4) of two different grain sizes, sandwiched between two layers of essentially non-reacting quartz sand (SiO2). A highly concentrated solution of barium chloride was injected to create an asymmetric flow field. Once the barium chloride reached the reactive layer, it forced the transformation of strontium sulfate into barium sulfate (BaSO4). Due to the higher molar volume of barium sulfate, its precipitation caused a decrease of porosity and lowered the permeability. Changes in the flow field were observed with help of dye tracer tests. The experiments were modelled using the reactive transport code OpenGeosys-GEM. Tests with non-reactive tracers performed prior to barium chloride injection, as well as the density-driven flow (due to the high concentration of barium chloride solution), could be well reproduced by the numerical model. To reproduce the mineral bulk transformation with time, two populations of strontium sulfate grains with different kinetic rates of dissolution were applied. However, a default porosity permeability relationship was unable to account for measured pressure changes. Post mortem analysis of the strontium sulfate reactive medium provided useful information on the chemical and structural changes occurring at the pore scale at the interface that were considered in our model to reproduce the pressure evolution with time.

  6. Expulsion of Barium and Methane at Mud Volcanoes in the Gulf of Mexico

    NASA Astrophysics Data System (ADS)

    Castellini, D. G.; Dickens, G. R.; Snyder, G. T.; Gilhooly, W. P.; Ruppel, C. D.

    2003-12-01

    Submarine mud volcanoes and cold-seeps along continental margins transfer methane from gas-charged marine sediments to the water column. Such methane venting is dynamic and may provide an important and variable supply of carbon to the ocean and atmosphere through time. Barite mounds and chimneys have been found around some modern mud volcanoes and seeps, and similar structures can be identified in the geological record (e.g., bedded barite deposits). These observations suggest that expelled methane-rich fluids are greatly enriched in dissolved barium. However, there are very few analyses of barium concentrations in these systems. Here, we examine the dissolved barium of pore fluids from a series of shallow piston cores across two submarine mud volcanoes in the Gulf of Mexico. Dissolved barium concentrations at 1.5 m below the seafloor at the Garden Bank volcano range from 18200 ? M at the center of the feature to 0.56 ? M on its flanks approximately 1 km away. Similarly, dissolved barium concentrations at the Mississippi Canyon volcano range from 15600 ? M to 0.50 ? M. Thus, the concentrations in the cores of the mud volcanoes are nominally 5 orders of magnitude greater than in mean ocean water ( ˜0.1 ? M). Anaerobic oxidation of upward flowing methane consumes sulfate, which leads to the dissolution of barite and release of barium to pore fluids. Because this mechanism alone cannot explain the extreme concentrations in the mud volcanoes, a deep source of barium may exist in the Gulf of Mexico strata. Our current work is focused on quantifying the fluxes and sedimentary fate of expelled barium at these locations. However, even if a large fraction of the barium precipitates adjacent to the sites of methane venting, fluid expulsion at mud volcanoes must significantly impact the barium cycle in the Gulf of Mexico. Conceivably, submarine mud volcanoes and cold-seeps along continental margins are a major source of barium to the deep ocean, a concept that has profound implications with respect to certain paleoceanographic reconstructions.

  7. Barium cyanide

    Integrated Risk Information System (IRIS)

    Barium cyanide ; CASRN 542 - 62 - 1 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Ef

  8. Influence of the Flow Rate on Dissolution and Precipitation Features during Percolation of CO2-Rich Sulfate Solutions through Limestone Fractured Samples

    NASA Astrophysics Data System (ADS)

    Luquot, L.; Garcia-Rios, M.; Cama, J.; Soler Matamala, J. M.

    2014-12-01

    A test site for a prospective CO2 geological storage is situated in Hontomín (Burgos, northern Spain) with a reservoir rock that is composed of limestone (calcite). Calcite dissolution and gypsum precipitation are expected to occur when injecting CO2 in a limestone reservoir with sulfate-rich resident brine. If the reservoir is fractured, these reactions will take place mainly in the fractures which serve as conduits for flow of fluids. As a consequence, the structure of the fractures will vary leading to changes in their hydraulic and transport properties. In this study, a set of percolation experiments which consisted of injecting CO2-rich solutions through limestone fractured cores were performed under P = 150 bar and T = 60 ºC. Different flow rates ranging from 0.2 to 60 mL/h and sulfate-rich and sulfate-free solutions were used. Variation in fracture volume induced by calcite dissolution and gypsum precipitation was measured by means of X-ray computed microtomography (XCMT) and aqueous chemistry. An increase in flow rate led to an increase in volume of dissolved limestone per unit of time, which indicated that calcite dissolution in the fracture was transport controlled. Moreover, the dissolution pattern varied from face dissolution to wormhole formation and uniform dissolution by increasing the flow rate (i.e., Pe from 1 to 346). Fracture permeability always increased and depended on the forming dissolution pattern.

  9. Presence of sulfate does not inhibit low-temperature dolomite precipitation Mnica Snchez-Romn a,b,c,

    E-print Network

    Gilli, Adrian

    . Introduction The origin of dolomite remains a long-standing enigma in sedimentary geology mainly because of its- tures (200 °C), which indicated that the presence of small concentra- tions of sulfate inhibits

  10. Radar and satellite studies of the impact of mesoscale convective precipitation and wind systems on visibility, sulfates, and oxidants during persistent elevated pollution episodes

    SciTech Connect

    Lyons, W.A.; Calby, R.H.

    1983-06-01

    The results are consistent and supportive, but certainly not conclusive, of a hypothesis suggesting that PBL sulfate mass removal into the free troposphere are on the order of several times that deposited on the surface during convective rainfalls. Thus, given the highly episodic nature of wet deposition and the potential major contribution of a single event to a season's total, a need exists to better understand the contributions of the various MCPS types to visibility improvement and sulfate removal, both to the surface and especially into the free atmosphere. Few projects are cited in the literature in which the precipitation chemistry data were even crudely stratified into major storm types though Raynor and Hayes did find significantly higher surface deposition during frontal thunderstorms and squall lines. Hales and Dana suggest the importance of designing an experiment to achieve an accurate closure of species mass balance within the entire domain of a convective storm. In noting the extreme variability in species washout over a region, they speculate that the bulk of the variability within and between storms must occur by superposition of the effects of inhomogeneous storm features, as well as source characteristics. Grant stated that a definitive characterization of individual storm dynamics and trajectories must be performed before long-term trends can be established with certainty. From the viewpoint of a severe storms meteorologist, much of the effort ongoing to understand regional wet deposition, sulfate, ozone, and visibility patterns, is subject to large errors of interpretation unless an attempt is made to better understand the highly different ways in which various precipitation systems, convective and stratiform, impact the PBL.

  11. Extraction and characterization of lignin from oil palm biomass via ionic liquid dissolution and non-toxic aluminium potassium sulfate dodecahydrate precipitation processes.

    PubMed

    Mohtar, S S; Tengku Malim Busu, T N Z; Md Noor, A M; Shaari, N; Yusoff, N A; Bustam Khalil, M A; Abdul Mutalib, M I; Mat, H B

    2015-09-01

    The objective of this study is to extract and characterize lignin from oil palm biomass (OPB) by dissolution in 1-butyl-3-methylimidazolium chloride ([bmim][Cl]), followed by the lignin extraction through the CO2 gas purging prior to addition of aluminum potassium sulfate dodecahydrate (AlK(SO4)2 · 12H2O). The lignin yield, Y(L) (%wt.) was found to be dependent of the types of OPB observed for all precipitation methods used. The lignin recovery, RL (%wt.) obtained from CO2-AlK(SO4)2 · 12H2O precipitation was, however dependent on the types of OPB, which contradicted to that of the acidified H2SO4 and HCl solutions of pH 0.7 and 2 precipitations. Only about 54% of lignin was recovered from the OPB. The FTIR results indicate that the monodispersed lignin was successfully extracted from the OPT, OPF and OPEFB having a molecular weight (MW) of 1331, 1263 and 1473 g/mol, and degradation temperature of 215, 207.5 and 272 °C, respectively. PMID:26038325

  12. Emission spectrographic determination of barium in sea water using a cation exchange concentration procedure

    USGS Publications Warehouse

    Szabo, B. J.; Joensuu, O.

    1967-01-01

    A concentration technique employing Dowex 50W cation exchange resin is described for the determination of barium in sea water. The separated barium is precipitated as fluoride together with calcium and strontium and measured by emission spectrographic analysis. The vertical distribution of barium in sea water has been measured in the Caribbean Sea and the Atlantic Ocean. The barium content varied between 7 and 23 ??g. per liter; in two profiles, the lowest concentrations were at a depth of about 1000 meters.

  13. Barium enema (image)

    MedlinePLUS

    A barium enema is performed to examine the walls of the colon. During the procedure, a well lubricated enema tube is inserted gently into the rectum. The barium, a radiopaque (shows up on X-ray) contrast ...

  14. Effect of hydrolysis conditions on hydrous TiO2 polymorphs precipitated from a titanyl sulfate and sulfuric acid solution

    NASA Astrophysics Data System (ADS)

    Song, Hao; Liang, Bin; Lü, Li; Wu, Pan; Li, Chun

    2012-07-01

    The relationship between hydrolysis conditions and hydrous titania polymorphs obtained in a titanyl sulfate and sulfuric acid solution was investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HRTEM). The results revealed that the feeding rate of the titanyl sulfate stock solution, the concentration of sulfuric acid, and the seed dosage of rutile crystal could significantly affect the hydrolysis rate, thus influencing the titania crystal phase. Hydrous TiO2 in the form of rutile, anatase, or the mixture of both could be obtained in solutions of low titanium concentrations and 2.5wt% to 15wt% sulfuric acid at 100°C. When the hydrolysis rate of titanium expressed by TiO2 was more than or equal to 0.04 g/(L·min), the hydrolysate was almost phase-pure anatase, while the main phase state was rutile when the hydrolysis rate was less than or equal to 0.01 g/(L·min). With the hydrolysis rate between 0.02 and 0.03 g/(L·min), the hydrolysate contained almost equal magnitude of rutile and anatase. It seems that although rutile phase is thermodynamically stable in very acidic solutions, anatase is a kinetically stable phase.

  15. Production of a Pseudomonas lipase in n-alkane substrate and its isolation using an improved ammonium sulfate precipitation technique.

    PubMed

    Kanwar, Lambit; Gogoi, Binod Kumar; Goswami, Pranab

    2002-09-01

    Among the various lipidic and non-lipidic substances, normal alkanes within the chain lengths of C-12 to C-20 served as the best carbon substrates for the production of extracellular lipase by Pseudomonas species G6. Maximum lipase production of 25 U/ml of the culture broth was obtained by using n-hexadecane as the sole carbon substrate. The optimum pH of 8 and temperature of 34 + 1 degrees C were demonstrated for the production of lipase in n-hexadecane substrate. The optimum concentration of iron, which played a critical role on the lipase production, was found to be 0.25 mg/l. Lipase production could be enhanced to nearly 2.4-fold by using tributyrin at a concentration of 0.05% (v/v) in the culture medium. High recovery of the lipase protein (83%) from the culture broth was achieved by treating the culture supernatant with Silicone 21 Defoamer followed by ammonium sulfate (60% saturation) fractionation. PMID:12118695

  16. Barium release system

    NASA Technical Reports Server (NTRS)

    Lewis, B. W.; Stokes, C. S.; Smith, E. W.; Murphy, W. J. (inventors)

    1973-01-01

    A chemical system is described for releasing a good yield of free barium neutral atoms and barium ions in the upper atmosphere and interplanetary space for the study of the geophysical properties of the medium. The barium is released in the vapor phase so that it can be ionized by solar radiation and also be excited to emit resonance radiation in the visible range. The ionized luminous cloud of barium becomes a visible indication of magnetic and electrical characteristics in space and allows determination of these properties over relatively large areas at a given time.

  17. Sulfate scale dissolution

    SciTech Connect

    Morris, R.L.; Paul, J.M.

    1992-01-28

    This patent describes a method for removing barium sulfate scale. It comprises contacting the scale with an aqueous solution having a pH of about 8 to about 14 and consisting essentially of a chelating agent comprising a polyaminopolycarboxylic acid or salt of such an acid in a concentration of 0.1 to 1.0 M, and anions of a monocarboxylic acid selected form mercaptoacetic acid, hydroxyacetic acid, aminoacetic acid, or salicyclic acid in a concentration of 0.1 to 1.0 M and which is soluble in the solution under the selected pH conditions, to dissolve the scale.

  18. Radium and barium removal through blending hydraulic fracturing fluids with acid mine drainage.

    PubMed

    Kondash, Andrew J; Warner, Nathaniel R; Lahav, Ori; Vengosh, Avner

    2014-01-21

    Wastewaters generated during hydraulic fracturing of the Marcellus Shale typically contain high concentrations of salts, naturally occurring radioactive material (NORM), and metals, such as barium, that pose environmental and public health risks upon inadequate treatment and disposal. In addition, fresh water scarcity in dry regions or during periods of drought could limit shale gas development. This paper explores the possibility of using alternative water sources and their impact on NORM levels through blending acid mine drainage (AMD) effluent with recycled hydraulic fracturing flowback fluids (HFFFs). We conducted a series of laboratory experiments in which the chemistry and NORM of different mix proportions of AMD and HFFF were examined after reacting for 48 h. The experimental data combined with geochemical modeling and X-ray diffraction analysis suggest that several ions, including sulfate, iron, barium, strontium, and a large portion of radium (60-100%), precipitated into newly formed solids composed mainly of Sr barite within the first ? 10 h of mixing. The results imply that blending AMD and HFFF could be an effective management practice for both remediation of the high NORM in the Marcellus HFFF wastewater and beneficial utilization of AMD that is currently contaminating waterways in northeastern U.S.A. PMID:24367969

  19. Dissolution of Barium from Barite in Sewage Sludges and Cultures of Desulfovibrio desulfuricans

    PubMed Central

    Baldi, F.; Pepi, M.; Burrini, D.; Kniewald, G.; Scali, D.; Lanciotti, E.

    1996-01-01

    High concentrations of total barium, ranging from 0.42 to 1.58 mg(middot)g(sup-1) (dry weight) were found in sludges of two sewage treatment plants near Florence, Italy. Barium concentrations in the suspended matter decreased as redox potential values changed from negative to positive. An anoxic sewage sludge sample was aerated, and 30% of the total barium was removed in 24 h. To demonstrate that barium was solubilized from barite by sulfate-reducing bacteria, a strain of Desulfovibrio desulfuricans was used to study the solubilization of barium from barite under laboratory conditions. During cell growth with different concentrations of barite from 0.01 to 0.3 g(middot)liter(sup-1) (the latter is the MIC) as the only source of sulfates in the cultures, the D. desulfuricans strain accumulated barium up to 0.58 (mu)g(middot)mg(sup-1) (dry weight). Three times the quantity of barium was dissolved by bacteria than in the uninoculated medium (control). The unexpectedly low concentration of soluble barium (1.2 mg of Ba(middot)liter(sup-1)) with respect to the quantity expected (109 mg of Ba(middot)liter(sup-1)), calculated on the basis of the free H(inf2)S evolved from the dissimilatory reduction of sulfate from barite, was probably due to the formation of other barium compounds, such as witherite (BaCO(inf3)) and the transient species barium sulfide (BaS). The D. desulfuricans strain, growing on barite, formed visible aggregates. Confocal microscopy analysis showed that aggregates consisted of bacteria and barite. After 3 days of incubation, several autofluorescent crystals surrounded by a dissolution halo were observed. The crystals were identified as BaS by comparison with the commercial compound. PMID:16535353

  20. Observed Barium Emission Rates

    NASA Technical Reports Server (NTRS)

    Stenbaek-Nielsen, H. C.; Wescott, E. M.; Hallinan, T. J.

    1993-01-01

    The barium releases from the CRRES satellite have provided an opportunity for verifying theoretically calculated barium ion and neutral emission rates. Spectra of the five Caribbean releases in the summer of 1991 were taken with a spectrograph on board a U.S. Air Force jet aircraft. Because the line of sight release densities are not known, only relative rates could be obtained. The observed relative rates agree well with the theoretically calculated rates and, together with other observations, confirm the earlier detailed theoretical emission rates. The calculated emission rates can thus with good accuracy be used with photometric observations. It has been postulated that charge exchange between neutral barium and oxygen ions represents a significant source for ionization. If so. it should be associated with emissions at 4957.15 A and 5013.00 A, but these emissions were not detected.

  1. Isotopic Zonation Within Sulfate Evaporite Mineral Crystals Reveal Quantitative Paleoenvironment Details

    NASA Astrophysics Data System (ADS)

    Coleman, M.; Rhorssen, M.; Mielke, R. E.

    2008-12-01

    Isotopic variations measured within a single crystal of hydrated magnesium sulfate are greater than 30 permil for delta 2-H, almost 10 permil for ?18O in water of hydration; and greater than 3 permil in sulfate oxygen. These results are interpreted to indicate the relative humidity of the system during evaporation (15 to 20 percent in this test case) and constrain the volume of water involved. The theoretical basis of this system is the isotopic fractionation between the species in solution and those precipitated as evaporite salts. Precipitation preferentially accumulates more of the heavy isotopes of sulfur and oxygen in mineral sulfate, relative to sulfate in solution. During the course of mineral growth this leads to successive depletion of the respective heavier isotopes in the residual brine reflected in a parallel trend in successive precipitates or even in successive zones within a single crystal. The change in isotopic composition at any one time during the process, relative to the initial value, can be described by an isotopic version of the Rayleigh Fractionation equation, depending only on the extent of the completion of the process and the relevant fractionation factor. Evaporation preferentially removes isotopically lighter hydrogen and oxygen leading to successive extents of enrichment in the respective heavier isotopes in the residual water. However, the relative effects on hydrogen and oxygen isotopes differs as function of relative humidity [1]. ALL OF THESE CHANGES ARE PRESERVED IN THE MINERAL ISOTOPE COMPOSITIONS. We precipitated barium sulfate from epsomite or gypsum samples, which was reduced at 1450°C in the presence of graphite and glassy carbon in a Finnigan TC/EA to produce CO for O isotopic analysis in a Finnigan 253 mass spectrometer, while a separate subsample was oxidized to SO2 in a Costech Elemental Analyzer. However, to make progress with this approach we needed to make a large number of measurements of hydration water and so we developed a new analytical method [2]. We use a modification of the standard TC/EA continuous-flow protocol to measure both hydrogen and oxygen of water of hydration from the same small sample. We have proved the concept of this new approach by analyzing zones within crystals and individual grains, growing epsomite (magnesium sulfate heptahydrate) in the laboratory and by analysis of natural gypsum evaporites. We are now exploring the effects of varying the controlling parameters. Eventual application to Martian sulfates will reveal amount of water involved in sulfate formation, its isotopic composition(s) and details of the paleo-atmospheric humidity. [1] Gat JR and Gonfiantini R, (Eds) (1981) IAEA Technical Report Series. [2] Rohrssen MK, Brunner B Mielke RE and Coleman M (2008) Analyt. Chem. (in press).

  2. Yielding Unexpected Results: Precipitation of Ba[subscript3](PO[subscript4])[subscript2] and Implications for Teaching Solubility Principles in the General Chemistry Curriculum

    ERIC Educational Resources Information Center

    Hazen, Jeffery L.; Cleary, David A.

    2014-01-01

    Precipitation of barium phosphate from aqueous solutions of a barium salt and a phosphate salt forms the basis for a number of conclusions drawn in general chemistry. For example, the formation of a solid white precipitate is offered as evidence that barium phosphate is insoluble. Furthermore, analysis of the supernatant is used to illustrate the…

  3. Barium and Compounds

    Integrated Risk Information System (IRIS)

    EPA / 635 / R - 05 / 001 www.epa.gov / iris TOXICOLOGICAL REVIEW OF BARIUM AND COMPOUNDS ( CAS No . 7440 - 39 - 3 ) In Support of Summary Information on the Integrated Risk Information System ( IRIS ) March 1998 Minor revisions January 1999 Reference dose revised June 2005 U.S . Environmental Protec

  4. Methods for producing monodispersed particles of barium titanate

    DOEpatents

    Hu, Zhong-Cheng (Knoxville, TN)

    2001-01-01

    The present invention is a low-temperature controlled method for producing high-quality, ultrafine monodispersed nanocrystalline microsphere powders of barium titanate and other pure or composite oxide materials having particles ranging from nanosized to micronsized particles. The method of the subject invention comprises a two-stage process. The first stage produces high quality monodispersed hydrous titania microsphere particles prepared by homogeneous precipitation via dielectric tuning in alcohol-water mixed solutions of inorganic salts. Titanium tetrachloride is used as an inorganic salt precursor material. The second stage converts the pure hydrous titania microsphere particles into crystalline barium titanate microsphere powders via low-temperature, hydrothermal reactions.

  5. Dissolution of [(226)Ra]BaSO4 and partial separation of (226)Ra from radium/barium sulfate: A new treatment method for NORM waste from petroleum industry.

    PubMed

    Al Abdullah, Jamal; Al Masri, M S; Amin, Yusr

    2016-01-01

    Complete dissolution of [(226)Ra]BaSO4 precipitate was successfully performed using NaNO2 as a reducing agent in acidic solution at room temperature. Results showed a significant effect of acid and NaNO2 concentrations and temperature on the dissolution efficiency. The method was successfully used for separation of radium from NORM scale samples from the petroleum industry; sufficient volume reduction of NORM waste was achieved. The obtained (226)Ra solution was purified using two separation methods. The dissolution method can be of great interest in the development of radiochemical analysis of radium isotopes. PMID:26623931

  6. Glucosamine sulfate

    MedlinePLUS

    ... to control arthritis pain. These creams usually contain camphor and other ingredients in addition to glucosamine. Researchers ... in combination with chondroitin sulfate, shark cartilage, and camphor for up to 8 weeks. Glucosamine sulfate can ...

  7. 75 FR 33824 - Barium Chloride From China

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-06-15

    ...731-TA-149 (Third Review)] Barium Chloride From China Determination On the basis...the antidumping duty order on barium chloride from China would be likely to lead to...4157 (June 2010), entitled Barium Chloride from China: Investigation No....

  8. 75 FR 19657 - Barium Chloride From China

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-04-15

    ...731-TA-149 (Third Review)] Barium Chloride From China AGENCY: United States International...the antidumping duty order on barium chloride from China...the antidumping duty order on barium chloride from China would be likely to lead...

  9. Silicosis in barium miners.

    PubMed Central

    Seaton, A; Ruckley, V A; Addison, J; Brown, W R

    1986-01-01

    Four men who mined barytes in Scotland and who developed pneumoconiosis are described. Three developed progressive massive fibrosis, from which two died; and one developed a nodular simple pneumoconiosis after leaving the industry. The radiological and pathological features of the men's lungs were those of silicosis and high proportions of quartz were found in two of them post mortem. The quartz was inhaled from rocks associated with the barytes in the mines. The features of silicosis in barium miners are contrasted with the benign pneumoconiosis, baritosis, that occurs in workers exposed to crushed and ground insoluble barium salts. Diagnostic difficulties arise when silicosis develops in workers mining minerals known to cause a separate and benign pneumoconiosis. These difficulties are compounded when, as not infrequently happens, the silicotic lesions develop or progress after exposure to quartz has ceased. Images PMID:3787542

  10. Comparing the relationship between precipitation and river geochemistry

    NASA Astrophysics Data System (ADS)

    Epp, A.; Luymes, R.; Bennett, M.; DaSilva, J.; Marsh, S. J.; Gillies, S. L.; Peucker-Ehrenbrink, B.; Voss, B.

    2013-12-01

    The geochemistry of precipitation affects the geochemistry of river water. Ideally, studies of river biogeochemistry should therefore include collection and analyses of dry and wet deposition. The Global Rivers Observatory has studied the Fraser River near Vancouver since the summer of 2009 at roughly bi-weekly resolution. The interpretation of this temporal record of river biogeochemistry, particularly the various sources of solutes, could be improved with a better understanding of atmospheric contributions. In this study precipitation and river water will be analysed from the Fraser River basin for nutrients as well as major and select trace ion concentrations. The nutrients analyzed will include ammonium (NH4), nitrate and nitrate (NO3-NO2), phosphate (PO4) and silicate (SiO4). Major ions include sodium (Na), potassium (K), calcium (Ca), magnesium (Mg), chloride (Cl), and sulfate (SO4). Trace elements may include molybdenum, strontium, barium, uranium, rubidium, manganese and iron. Samples will be collected using the bulk method which collects both wet and dry deposition . Correlating precipitation chemistry with data on wind direction may help elucidate sources of nutrients and major ions. For instance, westerly sources may transport pollution from the City of Vancouver and agricultural lands in the Fraser delta. Such pollutants may increase the acidity of precipitation and imprint the water chemistry with a unique chemical signature . The results of this study will be helpful in correcting Fraser River water data for contributions from atmospheric deposition.

  11. A model validation study of the washout/rainout contribution of sulfate and nitrate in wet deposition compared with precipitation chemistry data in Japan

    NASA Astrophysics Data System (ADS)

    Kajino, Mizuo; Aikawa, Masahide

    2015-09-01

    We simulated washout/rainout ratios of non-sea-salt (nss)-SO42- and NO3- using a chemical transport model and compared the estimates with precipitation measurements sampled at 0.5/1 mm intervals at sites located in Kobe (urban), Toyo-oka (suburban), and Tamba (rural) cities, Japan. The 25th and 75th percentile range of the simulated washout contributions was 30-70%. The simulated washout contribution range of NO3- (40-70%) was greater than that of nss-SO42 - (30-60%). There was good agreement between the simulated and observed values, and the observed washout contribution of NO3- was also greater than that of SO42-. The simulated washout contribution range was higher (60-75%) in emission source regions and lower (40-55%) in downwind areas. The wet deposition process is one of the key causes of uncertainty in chemical transport modeling. Comparing model results with such high-frequency precipitation chemistry data has been extremely rare. Thus the current study is providing useful information for evaluating and improving wet deposition modeling and for the better understanding of the wet deposition mechanism.

  12. Barium uranyl diphosphonates

    SciTech Connect

    Nelson, Anna-Gay D.; Alekseev, Evgeny V.; Ewing, Rodney C.; Albrecht-Schmitt, Thomas E.

    2012-08-15

    Three Ba{sup 2+}/UO{sub 2}{sup 2+} methylenediphosphonates have been prepared from mild hydrothermal treatment of uranium trioxide, methylendiphosphonic acid (C1P2) with barium hydroxide octahydrate, barium iodate monohydrate, and small aliquots of HF at 200 Degree-Sign C. These compounds, Ba[UO{sub 2}[CH{sub 2}(PO{sub 3}){sub 2}]{center_dot}1.4H{sub 2}O (Ba-1), Ba{sub 3}[(UO{sub 2}){sub 4}(CH{sub 2}(PO{sub 3}){sub 2}){sub 2}F{sub 6}]{center_dot}6H{sub 2}O (Ba-2), and Ba{sub 2}[(UO{sub 2}){sub 2}(CH{sub 2}(PO{sub 3}){sub 2})F{sub 4}]{center_dot}5.75H{sub 2}O (Ba-3) all adopt layered structures based upon linear uranyl groups and disphosphonate molecules. Ba-2 and Ba-3 are similar in that they both have UO{sub 5}F{sub 2} pentagonal bipyramids that are bridged and chelated by the diphosphonate moiety into a two-dimensional zigzag anionic sheet (Ba-2) and a one-dimensional ribbon anionic chain (Ba-3). Ba-1, has a single crystallographically unique uranium metal center where the C1P2 ligand solely bridges to form [UO{sub 2}[CH{sub 2}(PO{sub 3}){sub 2}]{sup 2-} sheets. The interlayer space of the structures is occupied by Ba{sup 2+}, which, along with the fluoride ion, mediates the structure formed and maintains overall charge balance. - Graphical abstract: Illustration of the stacking of the layers in Ba{sub 3}[(UO{sub 2}){sub 4}(CH{sub 2}(PO{sub 3}){sub 2}){sub 2})F{sub 6}]{center_dot}6H{sub 2}O viewed along the c-axis. The structure is constructed from UO{sub 7} pentagonal bipyramidal units, U(1)O{sub 7}=gray, U(2)O{sub 7}=yellow, barium=blue, phosphorus=magenta, fluorine=green, oxygen=red, carbon=black, and hydrogen=light peach. Highlights: Black-Right-Pointing-Pointer The polymerization of the UO{sub 2}{sup 2+} sites to form uranyl dimers leads to structural variations in compounds. Black-Right-Pointing-Pointer Barium cations stitch uranyl diphosphonate anionic layers together, and help mediate structure formation. Black-Right-Pointing-Pointer HF acts as both a mineralizing agent and a ligand.

  13. Sources of sulfate supporting anaerobic metabolism in a contaminated aquifer

    USGS Publications Warehouse

    Ulrich, G.A.; Breit, G.N.; Cozzarelli, I.M.; Suflita, J.M.

    2003-01-01

    Field and laboratory techniques were used to identify the biogeochemical factors affecting sulfate reduction in a shallow, unconsolidated alluvial aquifer contaminated with landfill leachate. Depth profiles of 35S-sulfate reduction rates in aquifer sediments were positively correlated with the concentration of dissolved sulfate. Manipulation of the sulfate concentration in samples revealed a Michaelis-Menten-like relationship with an apparent Km and Vmax of approximately 80 and 0.83 ??M SO4-2??day-1, respectively. The concentration of sulfate in the core of the leachate plume was well below 20 ??M and coincided with very low reduction rates. Thus, the concentration and availability of this anion could limit in situ sulfate-reducing activity. Three sulfate sources were identified, including iron sulfide oxidation, barite dissolution, and advective flux of sulfate. The relative importance of these sources varied with depth in the alluvium. The relatively high concentration of dissolved sulfate at the water table is attributed to the microbial oxidation of iron sulfides in response to fluctuations of the water table. At intermediate depths, barite dissolves in undersaturated pore water containing relatively high concentrations of dissolved barium (???100 ??M) and low concentrations of sulfate. Dissolution is consistent with the surface texture of detrital barite grains in contact with leachate. Laboratory incubations of unamended and barite-amended aquifer slurries supported the field observation of increasing concentrations of barium in solution when sulfate reached low levels. At a deeper highly permeable interval just above the confining bottom layer of the aquifer, sulfate reduction rates were markedly higher than rates at intermediate depths. Sulfate is supplied to this deeper zone by advection of uncontaminated groundwater beneath the landfill. The measured rates of sulfate reduction in the aquifer also correlated with the abundance of accumulated iron sulfide in this zone. This suggests that the current and past distributions of sulfate-reducing activity are similar and that the supply of sulfate has been sustained at these sites.

  14. Membranes solve North Sea waterflood sulfate problems

    SciTech Connect

    Davis, R.; Lomax, I.; Plummer, M.

    1996-11-25

    To prevent barium sulfate scale from forming in the North Sea Brae field producing wells, Marathon Oil Co. UK Ltd. is successfully employing thin-film composite (nanofiltration) membranes for removing sulfate from injected seawater. In the early 1980s, FilmTec Corp., a Dow Chemical Co. subsidiary, first developed these composite membranes, which now are in their third generation. Marathon Oil Co. holds the patent for the specific nanofiltration membrane process for mitigating scale formation and deleterious reservoir effects. This first article in a three-part series describes membrane technology. The remaining articles detail specific membrane performance characteristics and field experiences in the Brae fields.

  15. Characterization of sulfate ion in travertine

    NASA Astrophysics Data System (ADS)

    Takano, Bokuichiro; Asano, Yasuhiro; Watanuki, Kunihiko

    1980-04-01

    The mode of incorporation of sulfate ion in travertine was discussed on the basis of chemical compositions, i.r. and laser Raman spectra. These data strongly suggest that most of the sulfate ions in the calcitic travertine replace carbonate ions. This conclusion is in good harmony with the facts that calcite incorporates more sulfate ions than aragonite does and that the sulfate content of manganoan calcite decreases with increasing manganese content (Takano et al. 1977). Based on this conclusion, retarding effect of sulfate ion on the precipitation of calcite from solution was discussed.

  16. Discovery of the Barium Isotopes

    E-print Network

    A. Shore; A. Fritsch; J. Q. Ginepro; M. Heim; A. Schuh; M. Thoennessen

    2009-08-13

    Thirty-eight barium isotopes have so far been observed; the discovery of these isotopes is discussed. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented.

  17. Discovery of the barium isotopes

    SciTech Connect

    Shore, A.; Fritsch, A.; Ginepro, J.Q.; Heim, M.; Schuh, A.; Thoennessen, M.

    2010-11-15

    Thirty-eight barium isotopes have been observed so far and the discovery of these isotopes is discussed here. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented.

  18. Chondroitin sulfate

    MedlinePLUS

    ... with other products, including manganese ascorbate, glucosamine sulfate, glucosamine hydrochloride, or N-acetyl glucosamine. Research from a couple ... Early evidence suggests that chondroitin, with or without glucosamine hydrochloride, can reduce pain in people with Kashin-Beck ...

  19. Chondroitin sulfate

    MedlinePLUS

    ... sodium chondroitin sulfate into the bladder through a urinary catheter improves quality of live in people with overactive bladder. Urinary tract infections (UTIs). Early evidence suggests that ... (IALURIL) through a catheter weekly for 4 weeks and then monthly for ...

  20. Glucosamine sulfate

    MedlinePLUS

    ... be cautious about taking products that contain glucosamine. Diabetes: Some early research suggested that glucosamine sulfate might raise blood sugar in people with diabetes. However, more recent and more reliable research now ...

  1. Barium light source method and apparatus

    NASA Technical Reports Server (NTRS)

    Curry, John J. (Inventor); MacDonagh-Dumler, Jeffrey (Inventor); Anderson, Heidi M. (Inventor); Lawler, James E. (Inventor)

    2002-01-01

    Visible light emission is obtained from a plasma containing elemental barium including neutral barium atoms and barium ion species. Neutral barium provides a strong green light emission in the center of the visible spectrum with a highly efficient conversion of electrical energy into visible light. By the selective excitation of barium ionic species, emission of visible light at longer and shorter wavelengths can be obtained simultaneously with the green emission from neutral barium, effectively providing light that is visually perceived as white. A discharge vessel contains the elemental barium and a buffer gas fill therein, and a discharge inducer is utilized to induce a desired discharge temperature and barium vapor pressure therein to produce from the barium vapor a visible light emission. The discharge can be induced utilizing a glow discharge between electrodes in the discharge vessel as well as by inductively or capacitively coupling RF energy into the plasma within the discharge vessel.

  2. Suicidal poisoning with barium chloride.

    PubMed

    Jourdan, S; Bertoni, M; Sergio, P; Michele, P; Rossi, M

    2001-06-15

    A 49-year-old male pharmacist suffering from depression phoned the emergency services telling of how he had ingested barium chloride. He was found semicomatose in bed and resuscitation attempts were to no avail and he died at the scene. A white plastic container labelled "Barium chloride... Poison", and a book with a writing on a blank page... "give sulphate... SO(4)" were found. At autopsy, 1l of whitish-yellow fluid was found in the stomach. Autopsy barium levels were: blood 9.9mg/l; bile 8.8mg/l; urine 6.3mg/l; gastric 10.0g/l. Cause of death was given as cardiorespiratory arrest due to barium chloride poisoning. The issue of barium toxicity in a variety of itatrogenic and non itatrogenic situation is discussed together with the two only other cases of suicidal barium ingestion, and the feasibility of early intervention at the scene by an emergency team. PMID:11376995

  3. Abundance analysis of barium and mild barium stars

    E-print Network

    R. Smiljanic; G. F. Porto de Mello; L. da Silva

    2007-04-02

    High signal to noise, high resolution spectra were obtained for a sample of normal, mild barium, and barium giants. Atmospheric parameters were determined from the FeI and FeII lines. Abundances for Na, Mg, Al, Si, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Sr, Y, Zr, Ba, La, Ce, Nd, Sm, Eu, and Gd, were determined from equivalent widths and model atmospheres in a differential analysis, with the red giant Eps Vir as the standard star. The different levels of s-process overabundances of barium and mild barium stars were earlier suggested to be related to the stellar metallicity. Contrary to this suggestion, we found in this work no evidence of barium and mild barium to having different range in metallicity. However, comparing the ratio of abundances of heavy to light s-process elements, we found some evidence that they do not share the same neutron exposure parameter. The exact mechanism controlling this difference is still not clear. As a by-product of this analysis we identify two normal red giants misclassified as mild barium stars. The relevance of this finding is discussed. Concerning the suggested nucleosynthetic effects possibly related to the s-process, for elements like Cu, Mn, V and Sc, we found no evidence for an anomalous behavior in any of the s-process enriched stars analyzed here. However, further work is still needed since a clear [Cu/Fe] vs. [Ba/H] anticorrelation exists for other s-process enriched objects.

  4. Barium swallow study in routine clinical practice: a prospective study in patients with chronic cough*,**

    PubMed Central

    Nin, Carlos Shuler; Marchiori, Edson; Irion, Klaus Loureiro; Paludo, Artur de Oliveira; Alves, Giordano Rafael Tronco; Hochhegger, Daniela Reis; Hochhegger, Bruno

    2013-01-01

    OBJECTIVE: To assess the routine use of barium swallow study in patients with chronic cough. METHODS: Between October of 2011 and March of 2012, 95 consecutive patients submitted to chest X-ray due to chronic cough (duration > 8 weeks) were included in the study. For study purposes, additional images were obtained immediately after the oral administration of 5 mL of a 5% barium sulfate suspension. Two radiologists systematically evaluated all of the images in order to identify any pathological changes. Fisher's exact test and the chi-square test for categorical data were used in the comparisons. RESULTS: The images taken immediately after barium swallow revealed significant pathological conditions that were potentially related to chronic cough in 12 (12.6%) of the 95 patients. These conditions, which included diaphragmatic hiatal hernia, esophageal neoplasm, achalasia, esophageal diverticulum, and abnormal esophageal dilatation, were not detected on the images taken without contrast. After appropriate treatment, the symptoms disappeared in 11 (91.6%) of the patients, whereas the treatment was ineffective in 1 (8.4%). We observed no complications related to barium swallow, such as contrast aspiration. CONCLUSIONS: Barium swallow improved the detection of significant radiographic findings related to chronic cough in 11.5% of patients. These initial findings suggest that the routine use of barium swallow can significantly increase the sensitivity of chest X-rays in the detection of chronic cough-related etiologies. PMID:24473762

  5. Observation and theory of the barium releases from the CRRES satellite

    NASA Technical Reports Server (NTRS)

    Bernhardt, P. A.; Huba, J. D.; Scales, W. A.; Wescott, E. M.; Stenbaek-Nielsen, H. C.

    1992-01-01

    The relationship between releases of barium from the NASA Combined Release and Radiation Effects Satellite (CRRES) and enhanced auroral activity is discussed with reference to observational data. Barium releases were conducted at a variety of altitudes and injection velocities, and plasma irregularities are reported as a result of the interactions. Auroral activity increased within 5 min of each release, and references are made to the effects on diamagnetic cavities, bulk ion motion, and stimulated electron and ion precipitation. Artificially created structured diamagnetic cavities are noted for each release, plasma waves are generated by the high-speed ion clouds, and enhanced ionization is found in the critical ionization-velocity process. Barium releases are effective in stimulating electron precipitation, and the observed irregularities are related to cycloid bunching of the initial ion distributions.

  6. Interaction between Barium Oxide and Barium Containing Chloride Melt

    NASA Astrophysics Data System (ADS)

    Nikolaeva, Elena V.; Zakiryanova, Irina D.; Korzun, Iraida V.; Bovet, Andrey L.; Antonov, Boris D.

    2015-05-01

    Thermal analysis was applied to determine the liquidus temperatures in the NaCl-KCl-BaCl2-BaO system, with BaO concentration varied from 0 to 6 mole%. The temperature dependence of the BaO solubility in the NaCl-KCl-BaCl2 eutectic melt was investigated; the thermodynamic parameters of BaO dissolution were calculated. The caloric effects of melting of the NaCl-KCl-BaCl2 eutectic with barium oxide and barium oxychloride additions were studied. The type, morphology, and composition of oxychloride ionic groupings in the melt were determined in situ using Raman spectroscopy.

  7. Dimethyl sulfate

    Integrated Risk Information System (IRIS)

    Dimethyl sulfate ; CASRN 77 - 78 - 1 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic E

  8. Diethyl sulfate

    Integrated Risk Information System (IRIS)

    Diethyl sulfate ; CASRN 64 - 67 - 5 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Ef

  9. Barium Ions for Quantum Computation Matthew Dietrich

    E-print Network

    Blinov, Boris

    Barium Ions for Quantum Computation Matthew Dietrich A dissertation submitted in partial of the manuscript made from microform." Signature Date #12;#12;University of Washington Abstract Barium Ions Department of Physics Barium ion is investigated as a hyperfine qubit. 137Ba+ is trapped in a linear Paul

  10. Flow-injection analysis. Spectrophotometric determination of sulfate ions in atmospheric deposits

    SciTech Connect

    Eremina, I.D.; Shpigun, L.K.; Zolotov, Yu.A.

    1988-03-10

    A method has been developed for the spectrophotometric determination of sulfate ions in atmospheric deposits using an automated flow-injection analysis system. The method is based on the masking by sulfates of the high-sensitivity reaction of barium with orthanyl K. Sulfate contents in the range 0.5-20 mg/liter can be determined at the rate of 40 samples/h.

  11. Removal of Sulfate Ion From AN-107 by Evaporation

    SciTech Connect

    GJ Lumetta; GS Klinger; DE Kurath; RL Sell; LP Darnell; LR Greenwood; CZ Soderquist; MJ Steele; MW Urie; JJ Wagner

    2000-08-02

    Hanford low-activity waste solutions contain sulfate, which can cause accelerated corrosion of the vitrification melter and unacceptable operating conditions. A method is needed to selectively separate sulfate from the waste. An experiment was conducted to evaluate evaporation for removing sulfate ion from Tank AN-107 low-activity waste. Two evaporation steps were performed. In the first step, the volume was reduced by 55% while in the second step, the liquid volume was reduced another 22%. Analysis of the solids precipitated during these evaporations revealed that large amounts of sodium nitrate and nitrite co-precipitated with sodium sulfate. Many other waste components precipitated as well. It can be concluded that sulfate removal by precipitation is not selective, and thus, evaporation is not a viable option for removing sulfate from the AN-107 liquid.

  12. 21 CFR 82.3 - Definitions.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...term blanc fixe means a suspension in water of precipitated barium sulfate. (i) The term gloss white means a suspension in water of co-precipitated aluminum hydroxide and barium sulfate. (j) The term mixed oxides means the...

  13. 21 CFR 82.3 - Definitions.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...term blanc fixe means a suspension in water of precipitated barium sulfate. (i) The term gloss white means a suspension in water of co-precipitated aluminum hydroxide and barium sulfate. (j) The term mixed oxides means the...

  14. 21 CFR 82.3 - Definitions.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...term blanc fixe means a suspension in water of precipitated barium sulfate. (i) The term gloss white means a suspension in water of co-precipitated aluminum hydroxide and barium sulfate. (j) The term mixed oxides means the...

  15. 21 CFR 82.3 - Definitions.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...term blanc fixe means a suspension in water of precipitated barium sulfate. (i) The term gloss white means a suspension in water of co-precipitated aluminum hydroxide and barium sulfate. (j) The term mixed oxides means the...

  16. 21 CFR 82.3 - Definitions.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...term blanc fixe means a suspension in water of precipitated barium sulfate. (i) The term gloss white means a suspension in water of co-precipitated aluminum hydroxide and barium sulfate. (j) The term mixed oxides means the...

  17. Distribution and source of barium in ground water at Cattaraugus Indian Reservation, southwestern New York

    USGS Publications Warehouse

    Moore, R.B.; Staubitz, W.W.

    1984-01-01

    High concentrations of dissolved barium have been found in ground water from bedrock wells on the Seneca Nation of Indians Reservation on Cattaraugus Creek in southwestern New York. Concentrations in 1982 were as high as 23.0 milligrams per liter , the highest found reported from any natural ground-water system in the world. The highest concentrations are in a bedrock aquifer and in small lenses of saturated gravel between bedrock and the overlying till. The bedrock aquifer is partly confined by silt, clay, and till. The high barium concentrations are attributed to dissolution of the mineral barite (BaSO4), which is present in the bedrock and possibly in overlying silt, clay, or till. The dissolution of barite seems to be controlled by action of sulfate-reducing bacteria, which alter the BaSO4 equilibrium by removing sulfate ions and permitting additional barite to dissolve. Ground water from the surficial, unconsolidated deposits and surface water in streams contain little or no barium. Because barium is chemically similar to calcium, it probably could be removed by cation exchange or treatments similar to those used for water softening. (USGS)

  18. The problem of the barium stars

    NASA Technical Reports Server (NTRS)

    Bohm-Vitense, E.; Nemec, J.; Proffitt, C.

    1984-01-01

    Ultraviolet observations of barium stars and other cool stars with peculiar element abundances are reported. Those observations attempted to find hot white dwarf companions. Among six real barium stars studied, only Zeta Cap was found to have a white dwarf companion. Among seven mild, or marginal, barium stars studied, at least three were found to have hot subluminous companions. It is likely that all of them have white dwarf companions.

  19. 75 FR 20625 - Barium Chloride From China

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-04-20

    ...INTERNATIONAL TRADE COMMISSION [Investigation No. 731-TA-149 (Third Review)] Barium Chloride From China AGENCY: United States International Trade Commission. ACTION: Revised schedule for the subject...

  20. The L equals 6.7 quiet time barium shaped charge injection experiment 'Chachalaca'

    NASA Technical Reports Server (NTRS)

    Wescott, E. M.; Stenbaek-Nielsen, H. C.; Davis, T. N.; Rieger, E. P.; Peek, H. M.; Bottoms, P. J.

    1975-01-01

    Near dawn on October 9, 1972, UT, a barium plasma injection experiment was carried out from Poker Flat, Alaska, during quiet magnetic conditions (Kp equals 1+). The visible plasma flux tube produced was more diffuse than the flux tubes in previous experiments, but it could be tracked for 30 min out to an altitude of 2.5 earth radii. The flux tube remained integral for about 20 min, when a single striation separated from the main streak. Comparisons of the observed flux tube orientation with theoretical field models show no significant deviations ascribable to field-aligned currents. Cross-field drift rates of the foot of the flux tube indicate an E field of approximately 7 mV/m at 200-km altitude. Although an attempt was made via a jet aircraft flight, barium ions were not detected in the southern conjugate region. No energetic particle precipitation phenomena were observed which could be ascribed to the barium plasma injection.

  1. Barium Depletion in Hollow Cathode Emitters

    NASA Technical Reports Server (NTRS)

    Polk, James E.; Capece, Angela M.; Mikellides, Ioannis G.; Katz, Ira

    2009-01-01

    The effect of tungsten erosion, transport and redeposition on the operation of dispenser hollow cathodes was investigated in detailed examinations of the discharge cathode inserts from an 8200 hour and a 30,352 hour ion engine wear test. Erosion and subsequent re-deposition of tungsten in the electron emission zone at the downstream end of the insert reduces the porosity of the tungsten matrix, preventing the ow of barium from the interior. This inhibits the interfacial reactions of the barium-calcium-aluminate impregnant with the tungsten in the pores. A numerical model of barium transport in the internal xenon discharge plasma shows that the barium required to reduce the work function in the emission zone can be supplied from upstream through the gas phase. Barium that flows out of the pores of the tungsten insert is rapidly ionized in the xenon discharge and pushed back to the emitter surface by the electric field and drag from the xenon ion flow. This barium ion flux is sufficient to maintain a barium surface coverage at the downstream end greater than 0.6, even if local barium production at that point is inhibited by tungsten deposits. The model also shows that the neutral barium pressure exceeds the equilibrium vapor pressure of the impregnant decomposition reaction over much of the insert length, so the reactions are suppressed. Only a small region upstream of the zone blocked by tungsten deposits is active and supplies the required barium. These results indicate that hollow cathode failure models based on barium depletion rates in vacuum dispenser cathodes are very conservative.

  2. REMOVAL OF BARIUM AND RADIUM FROM GROUNDWATER

    EPA Science Inventory

    A research project was undertaken to investigate processes for removing barium and radium from drinking water. Special emphasis was placed on ion exchange processes that can be used without adding large concentrations of sodium to the water. The wastes from radium and barium remo...

  3. Mössbauer and X-ray diffraction study of Co2+-Si4+ substituted M-type barium hexaferrite BaFe12-2????Si?O19±?

    NASA Astrophysics Data System (ADS)

    Solovyova, E. D.; Pashkova, E. V.; Ivanitski, V. P.; V?yunov, O. I.; Belous, A. G.

    2013-03-01

    Using X-ray powder diffractions, Mössbauer spectroscopy, and magnetic measurements, the effect of dopants (Co2++Si4+) on the fine structure and magnetic properties of M-type barium hexaferrite prepared by hydroxide and carbonate precipitations has been studied. It has been shown that the magnetic properties of M-type barium hexaferrite can be controlled by heterovalent substitution 2Fe3+???2++S?4+.

  4. Biological sulfate removal in an upflow packed-bed reactor

    SciTech Connect

    Maree, J.P.; Strydom, W.F.

    1984-01-01

    A biological process for the removal of sulfate, using molasses as organic carbon source, is described. Sulfate is converted to sulfur via sulfide, and molasses to bicarbonate. The process is accompanied by the precipitation of calcium carbonate and heavy-metal sulfides. Sulfate reduction follows zero-order kinetics with respect to both reactants and products. The reduction of 1 g sulfate consumes 1,2 ml molasses and requires 6 h for completion. The Darcian minimum upflow velocity for sulfate reduction in an anaerobic packed-bed reactor was found to be 1,3 m/h and the optimum temperature 31 C.

  5. Plasmid-encoded copper resistance and precipitation by Mycobacterium scrofulaceum

    SciTech Connect

    Frardi, F.X.; Failla, M.L.; Falkinham, J.O. III

    1987-08-01

    A copper-tolerant Mycobacterium scrofulaceum strain was able to remove copper from culture medium by sulfate-dependent precipitation as copper sulfide. Such precipitation of copper sulfide was not observed in a derivative that lacks a 173-kilobase plasmid. In addition, the plasmid-carrying strain has a sulfate-independent copper resistance mechanism.

  6. Communications to the Editor Synthesis of Monodisperse Nanoparticles of Barium

    E-print Network

    Communications to the Editor Synthesis of Monodisperse Nanoparticles of Barium Titanate: Toward of barium titanate, BaTiO3, with diameters ranging from 6 to 12 nm. Barium titanate is a room,10 In the synthesis developed here, barium titanium ethyl hexano-isopropoxide (A

  7. Novel Thermally Stable Poly (vinyl chloride) Composites for Sulfate Removal

    EPA Science Inventory

    BaCO3 dispersed PVC composites were prepared through a polymer re-precipitation method. The composites were tested for sulfate removal using rapid small scale column test (RSSCT) and found to significantly reduce sulfate concentration. The method was extended to synthe...

  8. Radium/Barium Waste Project

    SciTech Connect

    McDowell, Allen K.; Ellefson, Mark D.; McDonald, Kent M.

    2015-06-25

    The treatment, shipping, and disposal of a highly radioactive radium/barium waste stream have presented a complex set of challenges requiring several years of effort. The project illustrates the difficulty and high cost of managing even small quantities of highly radioactive Resource Conservation and Recovery Act (RCRA)-regulated waste. Pacific Northwest National Laboratory (PNNL) research activities produced a Type B quantity of radium chloride low-level mixed waste (LLMW) in a number of small vials in a facility hot cell. The resulting waste management project involved a mock-up RCRA stabilization treatment, a failed in-cell treatment, a second, alternative RCRA treatment approach, coordinated regulatory variances and authorizations, alternative transportation authorizations, additional disposal facility approvals, and a final radiological stabilization process.

  9. Abundance Analysis of Barium Stars

    E-print Network

    G. Q. Liu; Y. C. Liang; L. Deng

    2008-11-13

    We obtain the chemical abundances of six barium stars and two CH subgiant stars based on the high signal-to-noise ratio and high resolution Echelle spectra. The neutron capture process elements Y, Zr, Ba, La, Eu show obvious overabundance relative to the Sun, for example, their [Ba/Fe] values are from 0.45 to 1.27. Other elements, including Na, Mg, Al, Si, Ca, Sc, Ti, V, Cr, Mn, Ni, show comparable abundances to the Solar ones, and their [Fe/H] cover a range from $-$0.40 to 0.21, which means they belong to Galactic disk. The predicts of the theoretical model of wind accretion for binary systems can explain the observed abundance patterns of the neutron capture process elements in these stars, which means that their overabundant heavy-elements could be caused by accreting the ejecta of AGB stars, the progenitors of the present white dwarf companions in the binary systems.

  10. Geophysical disturbance environment during the NASA/MPE barium release at 5 earth radii on September 21, 1971.

    NASA Technical Reports Server (NTRS)

    Davis, T. N.; Stanley, G. M.; Boyd, J. S.

    1973-01-01

    The geophysical disturbance environment was quiet during the NASA/MPE barium release at 5 earth radii on September 21, 1971. At the time of the release, the magnetosphere was in the late recovery phase of a principal magnetic storm, the provisional Dst value was -13 gammas, and the local horizontal disturbance at Great Whale River was near zero. Riometer and other observations indicated low-level widespread precipitation of high-energy electrons at Great Whale River before, during, and after the release. Cloudy sky at this station prevented optical observation of aurora. No magnetic or ionospheric effects attributable to the barium release were detected at Great Whale River.

  11. Barium Isotopes in Single Presolar Grains

    NASA Technical Reports Server (NTRS)

    Pellin, M. J.; Davis, A. M.; Savina, M. R.; Kashiv, Y.; Clayton, R. N.; Lewis, R. S.; Amari, S.

    2001-01-01

    Barium isotopic compositions of single presolar grains were measured by laser ablation laser resonant ionization mass spectrometry and the implications of the data for stellar processes are discussed. Additional information is contained in the original extended abstract.

  12. Preparation and Characterization of Nano-particle Substituted Barium Hexaferrite

    E-print Network

    Atassi, Yomen; Tally, Mohammad

    2014-01-01

    High density magnetic recording requires high coercivity magnetic media and small particle size. Barium hexaferrite has been considered as a leading candidate material because of its chemical stability, fairly large crystal anisotropy and suitable magnetic characteristics. In this work, we present the preparation of the hexagonal ferrite BaFe12O19 and one of its derivative; the Zn-Sn substituted hexaferrite by the chemical co-precipitation method. The main advantage of this method on the conventional glass-ceramic one, resides in providing a small enough particle size for magnetic recording. We demonstrate using the X-ray diffraction patterns that the particle size decreases when substituting the hexaferrite by the Zn-Sn combination. This may improve the magnetic properties of the hexaferrite as a medium for HD magnetic recording

  13. Pulsating aurora induced by upper atmospheric barium releases

    NASA Technical Reports Server (NTRS)

    Deehr, C.; Romick, G.

    1977-01-01

    The paper reports the apparent generation of pulsating aurora by explosive releases of barium vapor near 250 km altitude. This effect occurred only when the explosions were in the path of precipitating electrons associated with the visible aurora. Each explosive charge was a standard 1.5 kg thermite mixture of Ba and CuO with an excess of Ba metal which was vaporized and dispersed by the thermite explosion. Traces of Sr, Na, and Li were added to some of the charges, and monitoring was achieved by ground-based spectrophotometric observations. On March 28, 1976, an increase in emission at 5577 A and at 4278 A was observed in association with the first two bursts, these emissions pulsating with roughly a 10 sec period for approximately 60 to 100 sec after the burst.

  14. Assessment of Barium Sulphate Formation and Inhibition at Surfaces with Synchrotron X-ray Diffraction (SXRD)

    SciTech Connect

    E Mavredaki; A Neville; K Sorbie

    2011-12-31

    The precipitation of barium sulphate from aqueous supersaturated solutions is a well-known problem in the oil industry often referred to as 'scaling'. The formation and growth of barite on surfaces during the oil extraction process can result in malfunctions within the oil facilities and serious damage to the equipment. The formation of barium sulphate at surfaces remains an important topic of research with the focus being on understanding the mechanisms of formation and means of control. In situ synchrotron X-ray diffraction (SXRD) was used to investigate the formation of barium sulphate on a stainless steel surface. The effect of Poly-phosphinocarboxylic acid (PPCA) and Diethylenetriamine-penta-methylenephosphonic acid (DETPMP) which are two commercial inhibitors for barium sulphate was examined. The in situ SXRD measurements allowed the identification of the crystal faces of the deposited barite in the absence and presence of the two inhibitors. The preferential effect of the inhibitors on some crystal planes is reported and the practical significance discussed.

  15. Cholesterol, Sulfate, and Heart Disease

    E-print Network

    Seneff, Stephanie

    Cholesterol, Sulfate, and Heart Disease Stephanie Seneff Wise Tradi0ons Workshop, London." -- Orville Wright #12;Outline · Introduc0on · Cholesterol sulfate · Blood clots #12;· Cholesterol sulfate supplies

  16. Thermochemical hydrogen production via a cycle using barium and sulfur - Reaction between barium sulfide and water

    NASA Technical Reports Server (NTRS)

    Ota, K.; Conger, W. L.

    1977-01-01

    The reaction between barium sulfide and water, a reaction found in several sulfur based thermochemical cycles, was investigated kinetically at 653-866 C. Gaseous products were hydrogen and hydrogen sulfide. The rate determining step for hydrogen formation was a surface reaction between barium sulfide and water. An expression was derived for the rate of hydrogen formation.

  17. Hydrometallurgical process for recovering iron sulfate and zinc sulfate from baghouse dust

    DOEpatents

    Zaromb, Solomon (95706 William Dr., Hinsdale, IL 60521); Lawson, Daniel B. (925 Putnam Dr., Lockport, IL 60441)

    1994-01-01

    A process for recovering zinc/rich and iron-rich fractions from the baghouse dust that is generated in various metallurgical operations, especially in steel-making and other iron-making plants, comprises the steps of leaching the dust by hot concentrated sulfuric acid so as to generate dissolved zinc sulfate and a precipitate of iron sulfate, separating the precipitate from the acid by filtration and washing with a volatile liquid, such as methanol or acetone, and collecting the filtered acid and the washings into a filtrate fraction. The volatile liquid may be recovered distillation, and the zinc may be removed from the filtrate by alternative methods, one of which involves addition of a sufficient amount of water to precipitate hydrated zinc sulfate at 10.degree. C., separation of the precipitate from sulfuric acid by filtration, and evaporation of water to regenerate concentrated sulfuric acid. The recovery of iron may also be effected in alternative ways, one of which involves roasting the ferric sulfate to yield ferric oxide and sulfur trioxide, which can be reconverted to concentrated sulfuric acid by hydration. The overall process should not generate any significant waste stream.

  18. Hydrometallurgical process for recovering iron sulfate and zinc sulfate from baghouse dust

    DOEpatents

    Zaromb, S.; Lawson, D.B.

    1994-02-15

    A process for recovering zinc-rich and iron-rich fractions from the baghouse dust that is generated in various metallurgical operations, especially in steel-making and other iron-making plants, comprises the steps of leaching the dust by hot concentrated sulfuric acid so as to generate dissolved zinc sulfate and a precipitate of iron sulfate, separating the precipitate from the acid by filtration and washing with a volatile liquid, such as methanol or acetone, and collecting the filtered acid and the washings into a filtrate fraction. The volatile liquid may be recovered by distillation, and the zinc may be removed from the filtrate by alternative methods, one of which involves addition of a sufficient amount of water to precipitate hydrated zinc sulfate at 10 C, separation of the precipitate from sulfuric acid by filtration, and evaporation of water to regenerate concentrated sulfuric acid. The recovery of iron may also be effected in alternative ways, one of which involves roasting the ferric sulfate to yield ferric oxide and sulfur trioxide, which can be reconverted to concentrated sulfuric acid by hydration. The overall process should not generate any significant waste stream. 1 figure.

  19. Crystallization of Chicken Egg White Lysozyme from Sulfate Salts

    NASA Technical Reports Server (NTRS)

    Forsythe, Elizabeth; Pusey, Marc

    1998-01-01

    It has been "known" that chicken egg white lysozyme does not crystallize from sulfate, particularly ammonium sulfate, salts, but instead gives amorphous precipitates. This has been the basis of several studies using lysozyme comparing macromolecule crystal nucleation and amorphous precipitation. Recently Ries-Kautt et al (Acta Cryst D50, (1994) 366) have shown that purified isoionic CEWL could be crystallized from low concentrations of sulfate at basic pH, and we subsequently showed that in fact CEWL could be purified in both the tetragonal and orthorhombic forms using ammonium sulfate over the pH range 4.0 to 7.8 (Acta Cryst D53, (1997) 795). We have now extended these observations to include a range of common sulfate salts, specifically sodium, potassium, rubidium, magnesium, and manganese sulfates. In all cases but the manganese sulfates both the familiar tetragonal and orthorhombic forms were obtained, with unit cell dimensions close to those known for the "classic" sodium chloride crystallized forms. Manganese sulfate has only yielded orthorhombic crystals to date. All crystallizations were carried out using low (typically less than or equal to 6 M) salt and high (greater than approximately 90 mg/ml) protein concentrations. As with ammonium sulfate, the tetragonal - orthorhombic phase shift appears to be a function of both the temperature and the protein concentration, with higher temperatures and concentrations favoring the orthorhombic and lower the tetragonal form. The phase change range is somewhat reduced for the sulfate salts, depending upon conditions being typically between approximately 15 - 20 C. Both the magnesium and manganese sulfates gave crystals at salt concentrations over 0.6 M as well, with magnesium sulfate giving a very slowly nucleating and growing hexagonal form. A triclinic crystal form, characterized by aggressively small crystals (typically 0.1 mm in size) has been occasionally obtained from ammonium sulfate. Finally, preliminary spot solubility determinations have suggested that in some cases the solubility increases with increasing salt concentrations.

  20. pH control of the structure, composition, and catalytic activity of sulfated zirconia

    SciTech Connect

    Ivanov, Vladimir K.; Materials Science Department, Moscow State University, Moscow 119991 ; Baranchikov, Alexander Ye.; Kopitsa, Gennady P.; Lermontov, Sergey A.; Yurkova, Lyudmila L.; Gubanova, Nadezhda N.; Petersburg Nuclear Physics Institute, Orlova Roscha, Gatchina 188300 ; Ivanova, Olga S.; Lermontov, Anatoly S.; Rumyantseva, Marina N.; Vasilyeva, Larisa P.; Sharp, Melissa; Pranzas, P. Klaus; Tretyakov, Yuri D.

    2013-02-15

    We report a detailed study of structural and chemical transformations of amorphous hydrous zirconia into sulfated zirconia-based superacid catalysts. Precipitation pH is shown to be the key factor governing structure, composition and properties of amorphous sulfated zirconia gels and nanocrystalline sulfated zirconia. Increase in precipitation pH leads to substantial increase of surface fractal dimension (up to {approx}2.7) of amorphous sulfated zirconia gels, and consequently to increase in specific surface area (up to {approx}80 m{sup 2}/g) and simultaneously to decrease in sulfate content and total acidity of zirconia catalysts. Complete conversion of hexene-1 over as synthesized sulfated zirconia catalysts was observed even under ambient conditions. - Graphical abstract: Surface fractal dimension of amorphous sulfated zirconia and specific surface area and catalytic activity of crystalline sulfated zirconia as a function of precipitation pH. Highlights: Black-Right-Pointing-Pointer Structural transformation of amorphous hydrous zirconia into sulfated zirconia is studied. Black-Right-Pointing-Pointer Precipitation pH controls surface fractal dimension of amorphous zirconia gels. Black-Right-Pointing-Pointer Precipitation pH is the key factor governing properties of sulfated zirconia.

  1. Temperature-dependent coherent oscillation in photorefractive relaxor strontium barium

    E-print Network

    Osnabrück, Universität

    Temperature-dependent coherent oscillation in photorefractive relaxor strontium barium niobate M of the photorefractive light-induced scattering (beam fanning) in Sr0.61Ba0.39Nb2O6 (strontium barium niobate) doped

  2. Constraining the oceanic barium cycle with stable barium isotopes

    NASA Astrophysics Data System (ADS)

    Cao, Zhimian; Siebert, Christopher; Hathorne, Ed C.; Dai, Minhan; Frank, Martin

    2016-01-01

    The distribution of barium (Ba) concentrations in seawater resembles that of nutrients and Ba has been widely used as a proxy of paleoproductivity. However, the exact mechanisms controlling the nutrient-like behavior, and thus the fundamentals of Ba chemistry in the ocean, have not been fully resolved. Here we present a set of full water column dissolved Ba (DBa) isotope (?137BaDBa) profiles from the South China Sea and the East China Sea that receives large freshwater inputs from the Changjiang (Yangtze River). We find pronounced and systematic horizontal and depth dependent ?137BaDBa gradients. Beyond the river influence characterized by generally light signatures (0.0 to + 0.3 ‰), the ?137BaDBa values in the upper water column are significantly higher (+ 0.9 ‰) than those in the deep waters (+ 0.5 ‰). Moreover, ?137BaDBa signatures are essentially constant in the entire upper 100 m, in which dissolved silicon isotopes are fractionated during diatom growth resulting in the heaviest isotopic compositions in the very surface waters. Combined with the decoupling of DBa concentrations and ?137BaDBa from the concentrations of nitrate and phosphate this implies that the apparent nutrient-like fractionation of Ba isotopes in seawater is primarily induced by preferential adsorption of the lighter isotopes onto biogenic particles rather than by biological utilization. The subsurface ?137BaDBa distribution is dominated by water mass mixing. The application of stable Ba isotopes as a proxy for nutrient cycling should therefore be considered with caution and both biological and physical processes need to be considered. Clearly, however, Ba isotopes show great potential as a new tracer for land-sea interactions and ocean mixing processes.

  3. PHOTOSENSITIVE CENTERS AND CHARGE TRANSFER PROCESSES IN BARIUM CALCIUM TITANATE

    E-print Network

    Malovichko, Galina

    PHOTOSENSITIVE CENTERS AND CHARGE TRANSFER PROCESSES IN BARIUM CALCIUM TITANATE G.MALOVICHKO, V@uos.de; vgrachev@uos.de; schirmer@uos.de Abstract The results of the study of charge transfer processes in barium of crystals from barium titanate (BT) family make them promising candidates for various applications

  4. Experiments with remote entanglement using single barium ions Nathan Kurz

    E-print Network

    Blinov, Boris

    Experiments with remote entanglement using single barium ions Nathan Kurz A dissertation submitted entanglement using single barium ions Nathan Kurz Chair of the Supervisory Committee: Dr. Boris B. Blinov Physics Department Barium ion qubits are trapped and Doppler cooled in a linear Paul trap and the tasks

  5. Ferroelectric Properties of Individual Barium Titanate Nanowires Investigated

    E-print Network

    Walsworth, Ronald L.

    Ferroelectric Properties of Individual Barium Titanate Nanowires Investigated by Scanned Probe on the ferroelectric properties of individual single-crystalline barium titanate nanowires. We show that nonvolatile report the scanned probe characterization of individual single-crystalline barium titanate (BaTiO3) nano

  6. 40 CFR 721.10011 - Barium calcium manganese strontium oxide.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...2010-07-01 false Barium calcium manganese strontium oxide. 721.10011 Section 721...721.10011 Barium calcium manganese strontium oxide. (a) Chemical substance and...identified as barium calcium manganese strontium oxide (PMN P-00-1124; CAS...

  7. 40 CFR 721.10011 - Barium calcium manganese strontium oxide.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 false Barium calcium manganese strontium oxide. 721.10011 Section 721...721.10011 Barium calcium manganese strontium oxide. (a) Chemical substance and...identified as barium calcium manganese strontium oxide (PMN P-00-1124; CAS...

  8. 40 CFR 721.10011 - Barium calcium manganese strontium oxide.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...2014-07-01 false Barium calcium manganese strontium oxide. 721.10011 Section 721...721.10011 Barium calcium manganese strontium oxide. (a) Chemical substance and...identified as barium calcium manganese strontium oxide (PMN P-00-1124; CAS...

  9. 40 CFR 721.10011 - Barium calcium manganese strontium oxide.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...2012-07-01 false Barium calcium manganese strontium oxide. 721.10011 Section 721...721.10011 Barium calcium manganese strontium oxide. (a) Chemical substance and...identified as barium calcium manganese strontium oxide (PMN P-00-1124; CAS...

  10. 40 CFR 721.10011 - Barium calcium manganese strontium oxide.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...2013-07-01 false Barium calcium manganese strontium oxide. 721.10011 Section 721...721.10011 Barium calcium manganese strontium oxide. (a) Chemical substance and...identified as barium calcium manganese strontium oxide (PMN P-00-1124; CAS...

  11. Barium adsorption on hydrogenated ? surfaces

    NASA Astrophysics Data System (ADS)

    Vlachos, D. S.; Papageorgopoulos, C. A.

    1996-11-01

    An experimental study of Ba and H adsorption on 0953-8984/8/45/015/img2 by Auger electron spectroscopy, thermal desorption spectroscopy, low-energy electron diffraction, electron energy loss spectroscopy, and work function measurements has been made. Measurements of hydrogen adsorption on a clean silicon surface have been made mainly for reference purposes. H on Si forms two different states, known as monohydride state 0953-8984/8/45/015/img3 and dihydride state 0953-8984/8/45/015/img4. Preadsorption of H made the surface order more stable without changing the sticking coefficient of Ba on the Si surface. The results supported the double-layer (DL) model for the first Ba layer on the monohydrided Si surface. Ba adatoms up to 0953-8984/8/45/015/img5 ML on the dihydride phase were relaxed at symmetric and equivalent sites following the 0953-8984/8/45/015/img6 symmetry of the restored Si surface. TDS measurements showed that during Ba adsorption on the monohydride phase some of the H atoms were removed from their initial adsorption sites, and a new H energy state was formed at 0953-8984/8/45/015/img7 which was attributed to the weakening of the Si - H bond in the presence of Ba adatoms. When Ba deposition took place on the dihydride phase, two new H states were successively developed. The first state at 0953-8984/8/45/015/img8 was attributed to 0953-8984/8/45/015/img9 formation, and the subsequent one to a complex Ba - H - Si compound near 0953-8984/8/45/015/img10. The presence of hydrogen caused a considerable delay of barium overlayer metallization, in contrast to the early metallization of alkali on hydrogenated surfaces.

  12. An assessment of the redistribution of Barium during diagenesis of Marcellus Shale

    NASA Astrophysics Data System (ADS)

    Renock, D.; Symcox, C.; Lanids, J. D.; Sharma, M.

    2012-12-01

    Produced water from the hydrofracturing of Marcellus Shale have been reported to contain barium at concentrations >4000 ppm (Gregory et al, 2011). Understanding the reactions responsible for the leaching of Ba into produced water is important for improving the economic viability of gas extraction and to mitigate environmental concerns. Core samples of Marcellus Shale from New York and Pennsylvania were shown to contain Ba in the range of 400-2200 ?g/g. In some of these samples, barite (BaSO4) grains are shown to be partially replaced by pyrite (massive and framboidal varieties) suggesting that Ba is remobilized in the zone of sulfate reduction sometime after sedimentation. Sequential extraction experiments show Ba being released into buffered acetic acid (carbonate fraction), aqua regia (sulfide fraction), and hydrofluoric acid (silicate fraction) extractions despite ~50% of the barium remaining undissolved as barite. Laser ablation ICP-MS showed negligible concentrations of Ba in calcite veins and elevated concentrations in areas of the shale that are predominantly clay + organics. These results suggest that some of the Ba is associated with the clay fraction of the shale (e.g., sorbed to clay surfaces as a result of the anoxic dissolution of barite). These results may inform future strategies for mitigating the release of barium into produced water.

  13. Methods for sulfate removal in liquid-phase catalytic hydrothermal gasification of biomass

    DOEpatents

    Elliott, Douglas C; Oyler, James

    2013-12-17

    Processing of wet biomass feedstock by liquid-phase catalytic hydrothermal gasification must address catalyst fouling and poisoning. One solution can involve heating the wet biomass with a heating unit to a pre-treatment temperature sufficient for organic constituents in the feedstock to decompose, for precipitates of inorganic wastes to form, for preheating the wet feedstock in preparation for subsequent removal of soluble sulfate contaminants, or combinations thereof. Processing further includes reacting the soluble sulfate contaminants with cations present in the feedstock material to yield a sulfate-containing precipitate and separating the inorganic precipitates and/or the sulfate-containing precipitates out of the wet feedstock. Having removed much of the inorganic wastes and the sulfate contaminants that can cause poisoning and fouling, the wet biomass feedstock can be exposed to the heterogenous catalyst for gasification.

  14. Methods for sulfate removal in liquid-phase catalytic hydrothermal gasification of biomass

    DOEpatents

    Elliott, Douglas C; Oyler, James R

    2014-11-04

    Processing of wet biomass feedstock by liquid-phase catalytic hydrothermal gasification must address catalyst fouling and poisoning. One solution can involve heating the wet biomass with a heating unit to a pre-treatment temperature sufficient for organic constituents in the feedstock to decompose, for precipitates of inorganic wastes to form, for preheating the wet feedstock in preparation for subsequent removal of soluble sulfate contaminants, or combinations thereof. Processing further includes reacting the soluble sulfate contaminants with cations present in the feedstock material to yield a sulfate-containing precipitate and separating the inorganic precipitates and/or the sulfate-containing precipitates out of the wet feedstock. Having removed much of the inorganic wastes and the sulfate contaminants that can cause poisoning and fouling, the wet biomass feedstock can be exposed to the heterogeneous catalyst for gasification.

  15. Barium Titanate and Bismuth Oxide Nanocomposites Barium titanate, BaTiO3, and bismuth oxide Bi2O3 are transparent materials with

    E-print Network

    Harmon, Julie P.

    Barium Titanate and Bismuth Oxide Nanocomposites Barium titanate, BaTiO3, and bismuth oxide Bi2O3 Wall in Tetragonal Barium Titanate", H. Chaib, F. Schlaphof, T. Otto and L. M. Eng, Journal of Physics

  16. Precipitation Recycling

    NASA Technical Reports Server (NTRS)

    Eltahir, Elfatih A. B.; Bras, Rafael L.

    1996-01-01

    The water cycle regulates and reflects natural variability in climate at the regional and global scales. Large-scale human activities that involve changes in land cover, such as tropical deforestation, are likely to modify climate through changes in the water cycle. In order to understand, and hopefully be able to predict, the extent of these potential global and regional changes, we need first to understand how the water cycle works. In the past, most of the research in hydrology focused on the land branch of the water cycle, with little attention given to the atmospheric branch. The study of precipitation recycling which is defined as the contribution of local evaporation to local precipitation, aims at understanding hydrologic processes in the atmospheric branch of the water cycle. Simply stated, any study on precipitation recycling is about how the atmospheric branch of the water cycle works, namely, what happens to water vapor molecules after they evaporate from the surface, and where will they precipitate?

  17. TCA precipitation.

    PubMed

    Koontz, Laura

    2014-01-01

    Trichloroacetic acid (TCA) precipitation of proteins is commonly used to concentrate protein samples or remove contaminants, including salts and detergents, prior to downstream applications such as SDS-PAGE or 2D-gels. TCA precipitation denatures the protein, so it should not be used if the protein must remain in its folded state (e.g., if you want to measure a biochemical activity of the protein). PMID:24674058

  18. Analysis of 26 Barium Stars I. Abundances

    E-print Network

    Dinah M. Allen; Beatriz Barbuy

    2006-04-03

    We present a detailed analysis of 26 barium stars, including dwarf barium stars, providing their atmospheric parameters (Teff, log g, [Fe/H], vt) and elemental abundances. We aim at deriving gravities and luminosity classes of the sample stars, in particular to confirm the existence of dwarf barium stars. Accurate abundances of chemical elements were derived. Abundance ratios between nucleosynthetic processes, by using Eu and Ba as representatives of the r- and s-processes are presented. High-resolution spectra with the FEROS spectrograph at the ESO-1.5m Telescope, and photometric data with Fotrap at the Zeiss telescope at the LNA were obtained. The atmospheric parameters were derived in an iterative way, with temperatures obtained from colour-temperature calibrations. The abundances were derived using spectrum synthesis for Li, Na, Al, alpha-, iron peak, s- and r-elements atomic lines, and C and N molecular lines. Atmospheric parameters in the range 4300 barium stars, were derived and showed that [X/Ba] vs. [Ba/H] and [X/Ba] vs. [Fe/H] present different behaviour as compared to [X/Eu] vs. [Eu/H] and [X/Eu] vs. [Fe/H], reflecting the different nucleosynthetic sites for the s- and r-processes.

  19. 75 FR 19657 - Barium Chloride From China

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-04-15

    ... Commission found that the domestic interested party group response to its notice of institution (74 FR 31757... Barium Chloride From China AGENCY: United States International Trade Commission. ACTION: Notice of... chloride from China. SUMMARY: The Commission hereby gives notice that it will proceed with a full...

  20. 75 FR 20625 - Barium Chloride From China

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-04-20

    ... established a schedule for the conduct of this review (74 FR 62587, November 30, 2010). Subsequently, counsel... From the Federal Register Online via the Government Printing Office INTERNATIONAL TRADE COMMISSION Barium Chloride From China AGENCY: United States International Trade Commission. ACTION: Revised...

  1. On the suppression of superconducting phase formation in YBCO materials by templated synthesis in the presence of a sulfated biopolymer

    NASA Astrophysics Data System (ADS)

    Smith, Elliott; Schnepp, Zoe; Wimbush, Stuart C.; Hall, Simon R.

    2008-11-01

    The use of biopolymers as templates to control superconductor crystallization is a recent phenomenon and is generating a lot of interest both from the superconductor community and in materials chemistry circles. This work represents a critical finding in the use of such biopolymers, in particular the contraindicatory nature of sulfur when attempting to affect a morphologically controlled synthesis. Synthesis of superconducting nanoparticles was attempted using carrageenan as a morphological template. Reactive sulfate groups on the biopolymer prevent this, producing instead significant quantities of barium sulfate nanotapes. By substituting the biopolymer for structurally analogous, non-sulfated agar, we show that superconducting nanoparticles could be successfully synthesized.

  2. Gas hydrate decomposition and migration of the sulfate/methane transition zone recorded by authigenic barite in cold seep sediments

    NASA Astrophysics Data System (ADS)

    Kasten, S.; Hensen, C.; Spiess, V.; Blumenberg, M.; Schneider, R. R.

    2010-12-01

    After deposition of sediments a whole suite of geochemical/biogeochemical and transport processes - subsumed under the term early diagenesis - can potentially alter the primary sediment composition. Post-depositional overprint is not only restricted to the topmost part of the sediment but well extends into more deeply buried sediments. A biogeochemical reaction front which is of particular importance for deep post-depositional alteration is the so-called sulfate/methane transition zone (SMTZ) where the anaerobic oxidation of methane (AOM) by sulfate occurs. This front is often located several meters to several tens of meters within the sediment and can heavily impact a number of sedimentary components and attributes - like carbonates, barite, iron oxide and iron sulfide minerals as well as rock magnetic properties (e.g., magnetic susceptibility). In this way the primary sediment composition is distinctly altered several thousands to tens of thousands of years after deposition. Identifying and quantifying such diagenetic overprint is of the utmost importance to accurately interpret the sedimentary record. In marine environments affected by hydrocarbon seepage and/or the presence of gas hydrates the geochemical zonation is often significantly condensed and the sulfate/methane transition zone is typically located close to the sediment surface - in this way impacting the initial sediment composition at relatively shallow depth. While the process of AOM induces the destruction of several primary sediment components it also goes along with the diagenetic formation of secondary signals. One of these diagenetically formed compounds is authigenic barite which precipitates slightly above the SMTZ. We demonstrate that - following the approach of Dickens (2001) - authigenic barite can be a valuable geochemical proxy to trace the downward migration of the SMTZ over time as a result of the decomposition of gas hydrates and/or a decrease in the upward flux of hydrocarbons. Reference Dickens, G.R. (2001) Sulfate profiles and barium fronts in sediment on the Blake Ridge: Present and past methane fluxes through a large gas hydrate reservoir. Geochim. Cosmochim. Acta, 65, 529-543.

  3. Trapped Barium Ions for Quantum ComputationTrapped Barium Ions for Quantum Computation V.Mirgon, G.Shu, A.Avril, M.Dietrich N.Kurz, E. Shahar, and B.B.Blinov

    E-print Network

    Blinov, Boris

    Trapped Barium Ions for Quantum ComputationTrapped Barium Ions for Quantum Computation V.Mirgon, G of Washington Seattle WA 98195 Trapped Barium Ions for Quantum ComputationTrapped Barium Ions for Quantum

  4. Uranium Immobilization by Sulfate-reducing Biofilms

    SciTech Connect

    Beyenal, Haluk; Sani, Rajesh K.; Peyton, Brent M.; Dohnalkova, Alice; Amonette, James E.; Lewandowski, Zbigniew

    2004-04-01

    Hexavalent uranium [U(VI)] was immobilized using biofilms of the sulfate-reducing bacterium (SRB) Desulfovibrio desulfuricans G20. The biofilms were grown in flat-plate continuous-flow reactors using lactate as the electron donor and sulfate as the electron acceptor. U(VI) was continuously fed into the reactor for 32 weeks at a concentration of 126 íM. During this time, the soluble U(VI) was removed (between 88 and 96% of feed) from solution and immobilized in the biofilms. The dynamics of U immobilization in the sulfate-reducing biofilms were quantified by estimating: (1) microbial activity in the SRB biofilm, defined as the hydrogen sulfide (H2S) production rate and estimated from the H2S concentration profiles measured using microelectrodes across the biofilms; (2) concentration of dissolved U in the solution; and (3) the mass of U precipitated in the biofilm. Results suggest that U was immobilized in the biofilms as a result of two processes: (1) enzymatically and (2) chemically, by reacting with microbially generated H2S. Visual inspection showed that the dissolved sulfide species reacted with U(VI) to produce a black precipitate. Synchrotron-based U L3-edge X-ray absorption near edge structure (XANES) spectroscopy analysis of U precipitated abiotically by sodium sulfide indicated that U(VI) had been reduced to U(IV). Selected-area electron diffraction pattern and crystallographic analysis of transmission electron microscope lattice-fringe images confirmed the structure of precipitated U as being that of uraninite.

  5. Precipitation Matters

    ERIC Educational Resources Information Center

    McDuffie, Thomas

    2007-01-01

    Although weather, including its role in the water cycle, is included in most elementary science programs, any further examination of raindrops and snowflakes is rare. Together rain and snow make up most of the precipitation that replenishes Earth's life-sustaining fresh water supply. When viewed individually, raindrops and snowflakes are quite…

  6. Precipitation Gage

    USGS Multimedia Gallery

    During August 2013, the Beaver Creek wildfire burned more than 114,000 acres near the south-central Idaho communities of Sun Valley, Ketchum, and Hailey. Partnering with Blaine County, the USGS installed a network of real-time precipitation gages in the burn area. Real-time information from the gage...

  7. Biogeochemical and Hydrologic Controls of High Explosives, Barium, and Nitrate Contamination in a Semiarid Alluvial Aquifer

    NASA Astrophysics Data System (ADS)

    Newman, B. D.; Hickmott, D. D.; Heikoop, J. M.; Gram, P.; Reid, K.; Tardiff, M.

    2002-12-01

    Outfalls from High Explosives (HE) production sites at Los Alamos National Laboratory discharged HE (primarily RDX, TNT, and HMX), barium, and nitrate into an alluvial aquifer system from 1944 to 1996. HE in alluvial waters range to over 300 ug/L. Barium and nitrate concentrations range to over 5000 ug/L and 2000 ug/L (as N), respectively. The contaminants show temporal and spatial changes in concentration in the aquifer. These changes are a strong function of variations in aquifer recharge/source contributions. However, there are additional contaminant-specific controls that are important. The HE species have significantly different solubilities and susceptibilities to degradation that control differences in their distributions. RDX and HMX are relatively resistant to degradation. However, we have observed small concentrations of RDX and HMX breakdown products. In situ pH values suggest that RDX and HMX degradation may occur from an inorganic, pH controlled, hydrolysis reaction. Degradation may also occur from biologic breakdown in localized or seasonal, strongly anaerobic environments. In contrast, TNT breakdown products are relatively common, and degradation can occur via photolysis, hydrolysis, or biological processes. Barium appears to be largely controlled by inorganic processes including precipitation of barium minerals (i.e., witherite and barite), and sorption. Nitrate concentrations can decrease through denitrification. This observation is consistent with other semiarid studies that show that these aquifers can be nitrogen starved. Some of the temporal variability in HE and nitrate concentrations may also be related to temporal variability in oxidizing/reducing conditions. This kind of variability is controlled by oxygenation during recharge and subsequent depletion of dissolved oxygen as a result of biological activity between recharge events.

  8. Nanoparticles of barium induce apoptosis in human phagocytes

    PubMed Central

    Mores, Luana; França, Eduardo Luzia; Silva, Núbia Andrade; Suchara, Eliane Aparecida; Honorio-França, Adenilda Cristina

    2015-01-01

    Purpose Nutrients and immunological factors of breast milk are essential for newborn growth and the development of their immune system, but this secretion can contain organic and inorganic toxins such as barium. Colostrum contamination with barium is an important issue to investigate because this naturally occurring element is also associated with human activity and industrial pollution. The study evaluated the administration of barium nanoparticles to colostrum, assessing the viability and functional activity of colostral mononuclear phagocytes. Methods Colostrum was collected from 24 clinically healthy women (aged 18–35 years). Cell viability, superoxide release, intracellular Ca2+ release, and phagocyte apoptosis were analyzed in the samples. Results Treatment with barium lowered mononuclear phagocyte viability, increased superoxide release, and reduced intracellular calcium release. In addition, barium increased cell death by apoptosis. Conclusion These data suggest that nanoparticles of barium in colostrum are toxic to cells, showing the importance of avoiding exposure to this element. PMID:26451108

  9. Engineering domain configurations for enhanced piezoelectricity in barium titanate single crystals

    E-print Network

    Li, Jiangyu

    Engineering domain configurations for enhanced piezoelectricity in barium titanate single crystals piezoelectric responses of barium titanate single crystals under different crystallographic orientations, and use it to explain the ultrahigh piezoelectric response recently observed in a 270 cut barium titanate

  10. Effect of antiscalants on precipitation of an RO concentrate: metals precipitated and particle characteristics for several water compositions.

    PubMed

    Greenlee, Lauren F; Testa, Fabrice; Lawler, Desmond F; Freeman, Benny D; Moulin, Philippe

    2010-04-01

    Inland brackish water reverse osmosis (RO) is economically and technically limited by the large volume of salty waste (concentrate) produced. The use of a controlled precipitation step, followed by solid/liquid separation (filtration), has emerged as a promising side-stream treatment process to treat reverse osmosis concentrate and increase overall system recovery. The addition of antiscalants to the RO feed prevents precipitation within the membrane system but might have a deleterious effect on a concentrate treatment process that uses precipitation to remove problematic precipitates. The effects of antiscalant type and concentration on salt precipitation and precipitate particle morphology were evaluated for several water compositions. The primary precipitate for the synthetic brackish waters tested was calcium carbonate; the presence of magnesium, sulfate, minor ions, and antiscalant compounds affected the amount of calcium precipitated, as well as the phases of calcium carbonate formed during precipitation. Addition of antiscalant decreased calcium precipitation but increased incorporation of magnesium and sulfate into precipitating calcium carbonate. Antiscalants prevented the growth of nucleated precipitates, resulting in the formation of small (100-200 nm diameter) particles, as well as larger (6-10 microm) particles. Elemental analysis revealed changes in composition and calcium carbonate polymorph with antiscalant addition and antiscalant type. Results indicate that the presence of antiscalants does reduce the extent of calcium precipitation and can worsen subsequent filtration performance. PMID:20172582

  11. Barium Titanate Nanoparticles for Biomarker Applications

    NASA Astrophysics Data System (ADS)

    Matar, O.; Posada, O. M.; Hondow, N. S.; Wälti, C.; Saunders, M.; Murray, C. A.; Brydson, R. M. D.; Milne, S. J.; Brown, A. P.

    2015-10-01

    A tetragonal crystal structure is required for barium titanate nanoparticles to exhibit the nonlinear optical effect of second harmonic light generation (SHG) for use as a biomarker when illuminated by a near-infrared source. Here we use synchrotron XRD to elucidate the tetragonal phase of commercially purchased tetragonal, cubic and hydrothermally prepared barium titanate (BaTiO3) nanoparticles by peak fitting with reference patterns. The local phase of individual nanoparticles is determined by STEM electron energy loss spectroscopy (EELS), measuring the core-loss O K-edge and the Ti L3-edge energy separation of the t2g, eg peaks. The results show a change in energy separation between the t2g and eg peak from the surface and core of the particles, suggesting an intraparticle phase mixture of the barium titanate nanoparticles. HAADF-STEM and bright field TEM-EDX show cellular uptake of the hydrothermally prepared BaTiO3 nanoparticles, highlighting the potential for application as biomarkers.

  12. Lanthanide doped strontium-barium cesium halide scintillators

    DOEpatents

    Bizarri, Gregory; Bourret-Courchesne, Edith; Derenzo, Stephen E.; Borade, Ramesh B.; Gundiah, Gautam; Yan, Zewu; Hanrahan, Stephen M.; Chaudhry, Anurag; Canning, Andrew

    2015-06-09

    The present invention provides for a composition comprising an inorganic scintillator comprising an optionally lanthanide-doped strontium-barium, optionally cesium, halide, useful for detecting nuclear material.

  13. Creating unstable velocity-space distributions with barium injections

    NASA Technical Reports Server (NTRS)

    Pongratz, M. B.

    1983-01-01

    Ion velocity-space distributions resulting from barium injections from orbiting spacecraft and shaped charges are discussed. Active experiments confirm that anomalous ionization processes may operate, but photoionization accounts for the production of the bulk of the barium ions. Pitch-angle diffusion and/or velocity-space diffusion may occur, but observations of barium ions moving upwards against gravity suggests that the ions retain a significant enough fraction of their initial perpendicular velocity to provide a mirror force. The barium ion plasmas should have a range of Alfven Mach numbers and plasma betas. Because the initial conditions can be predicted these active experiments should permit testing plasma instability hypotheses.

  14. Trends in pH, calcium, and sulfate of rivers in Atlantic Canada

    SciTech Connect

    Clair, T.A.; Whitfield, P.H.

    1983-01-01

    Acid precipitation is affecting the chemistry of rivers in Atlantic Canada. Long term records for pH, calcium, and sulfate from 11 rivers were fitted using time series models. Decreases in pH over time were found, but the results for calcium and sulfate were not consistent with the predicted model. The conceptual models used to understand the effects of acid precipitation on water chemistry did not adequately explain the observed changes.

  15. Effect of Barium Loading on the Desulfation of Pt-BaO/Al2O3 Studied by H2 TPRX, TEM, Sulfur K-edge XANES, and in Situ TR-XRD

    SciTech Connect

    Kim, Do Heui; Szanyi, Janos; Kwak, Ja Hun; Szailer, Tamas; Hanson, Jonathan; Wang, Chong M.; Peden, Charles HF

    2006-06-01

    Desulfation processes were investigated over sulfated Pt BaO/Al2O3 with different barium loading (8 wt% and 20 wt%) by using H2 temperature programmed reaction (TPRX), transmission electron microscope (TEM) with energy dispersive spectroscopy (EDS), sulfur K-edge X-ray absorption near-edge spectroscopy (XANES), and in situ time-resolved X-ray diffraction (TR-XRD) techniques. Both sulfated samples (8 wt% and 20 wt%) form sulfate species (primarily BaSO4) as evidenced by S K-edge XANES and in situ TR-XRD. However, the desulfation behavior is strongly dependant on the barium loading. Sulfated Pt BaO(8)/Al2O3, consisting predominantly of surface BaO/BaCO3 species, displays more facile desulfation by H2 at lower temperatures than sulfated Pt BaO(20)/Al2O3, a material containing primarily bulk BaO/BaCO3 species. Therefore, after desulfation with H2 up to 1073 K, the amount of the remaining sulfur species on the former, mostly as BaS, is much less than on the latter. This suggests that the initial morphology differences between the two samples play a crucial role in determining the extent of desulfation and the temperature at which it occurs. It is concluded that the removal of sulfur is significantly easier at lower barium loading. This finding can potentially be important in developing more sulfur resistant LNT catalyst systems.

  16. Acidic precipitation

    SciTech Connect

    Martin, H.C.

    1987-01-01

    At the International Symposium on Acidic Precipitation, over 400 papers were presented, and nearly 200 of them are included here. They provide an overview of the present state of the art of acid rain research. The Conference focused on atmospheric science (monitoring, source-receptor relationships), aquatic effects (marine eutrophication, lake acidification, impacts on plant and fish populations), and terrestrial effects (forest decline, soil acidification, etc.).

  17. Synthesis of Single-Crystalline Perovskite Nanorods Composed of Barium Titanate and Strontium Titanate

    E-print Network

    Walsworth, Ronald L.

    Synthesis of Single-Crystalline Perovskite Nanorods Composed of Barium Titanate and Strontium alkoxide precursors and 1 mmol of oleic acid (Aldrich, 99+%). The precursors, barium titanium isopropoxide

  18. Hydrothermal crystallization of barium titanate: Mechanisms of nucleation and growth

    NASA Astrophysics Data System (ADS)

    Chun, Chang-Min

    Barium titanate is synthesized under hydrothermal conditions by the reaction of a variety of titania precursors with aqueous solutions of Ba(OH)sb2 at 80sp°C. Particles processed at relatively low concentrations of Ba(OH)sb2 are micro-sized and highly aggregated, but increasing concentrations cause the particle size to decrease, resulting in nanometer-sized and fairly monodispersed particles. The change in particle size and morphology at various Ba(OH)sb2 concentrations is controlled by the dissolution of titania and precipitation of BaTiOsb3. In order to explain the origin of "raspberry-like" BaTiOsb3 particles and the generation of hierarchically ordered BaTiOsb3 aggregate comprised of primary, crystalline particles, which exhibit an unusually high degree of crystallographic alignment, the role of colloidal stability and therefore controlled aggregation of precipitated primary particles is taken into account. Formation of SrTiOsb3 on BaTiOsb3 particles reveal that two different morphologies for the growing SrTiOsb3 exists and that the form taken by SrTiOsb3 depends on the degree of supersaturation. In concentrated solutions, homogeneous nucleation and aggregation growth occur. In dilute solutions, heterogeneous nucleation and continuous growth of SrTiOsb3 promote epitaxial growth. BaTiOsb3 particles prepared by the alkoxide (Ti(OCsb3Hsb7)sb4) -hydroxide (Ba(OH)sb2) route under hydrothermal conditions show that secondary processed such as aggregation and recrystallization are important to control the particle size and morphology. Particle clustering, and rearrangement of nanometer-sized BaTiOsb3 particles, and particulate uniformity can then be explained in terms of solution reactions and colloidal behavior.

  19. Remediation of Acid Mine Drainage with Sulfate Reducing Bacteria

    ERIC Educational Resources Information Center

    Hauri, James F.; Schaider, Laurel A.

    2009-01-01

    Sulfate reducing bacteria have been shown to be effective at treating acid mine drainage through sulfide production and subsequent precipitation of metal sulfides. In this laboratory experiment for undergraduate environmental chemistry courses, students design and implement a set of bioreactors to remediate acid mine drainage and explain observed…

  20. Sulfate attack expansion mechanisms

    SciTech Connect

    Müllauer, Wolfram Beddoe, Robin E.; Heinz, Detlef

    2013-10-15

    A specially constructed stress cell was used to measure the stress generated in thin-walled Portland cement mortar cylinders caused by external sulfate attack. The effects of sulfate concentration of the storage solution and C{sub 3}A content of the cement were studied. Changes in mineralogical composition and pore size distribution were investigated by X-ray diffraction and mercury intrusion porosimetry, respectively. Damage is due to the formation of ettringite in small pores (10–50 nm) which generates stresses up to 8 MPa exceeding the tensile strength of the binder matrix. Higher sulfate concentrations and C{sub 3}A contents result in higher stresses. The results can be understood in terms of the effect of crystal surface energy and size on supersaturation and crystal growth pressure.

  1. BARIUM IN TEETH AS INDICATOR OF BODY BURDEN

    EPA Science Inventory

    A study was conducted to determine the biological availability of naturally occurring barium in a municipal drinking water by the analysis of barium in deciduous teeth of children. The grade school children of two Illinois towns were chosen for the study. The towns were chosen ba...

  2. 40 CFR 721.10011 - Barium calcium manganese strontium oxide.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Barium calcium manganese strontium... Specific Chemical Substances § 721.10011 Barium calcium manganese strontium oxide. (a) Chemical substance... manganese strontium oxide (PMN P-00-1124; CAS No. 359427-90-0) is subject to reporting under this...

  3. 40 CFR 721.10011 - Barium calcium manganese strontium oxide.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Barium calcium manganese strontium... Specific Chemical Substances § 721.10011 Barium calcium manganese strontium oxide. (a) Chemical substance... manganese strontium oxide (PMN P-00-1124; CAS No. 359427-90-0) is subject to reporting under this...

  4. 40 CFR 721.10011 - Barium calcium manganese strontium oxide.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Barium calcium manganese strontium... Specific Chemical Substances § 721.10011 Barium calcium manganese strontium oxide. (a) Chemical substance... manganese strontium oxide (PMN P-00-1124; CAS No. 359427-90-0) is subject to reporting under this...

  5. 40 CFR 721.10011 - Barium calcium manganese strontium oxide.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Barium calcium manganese strontium... Specific Chemical Substances § 721.10011 Barium calcium manganese strontium oxide. (a) Chemical substance... manganese strontium oxide (PMN P-00-1124; CAS No. 359427-90-0) is subject to reporting under this...

  6. 40 CFR 721.10011 - Barium calcium manganese strontium oxide.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Barium calcium manganese strontium... Specific Chemical Substances § 721.10011 Barium calcium manganese strontium oxide. (a) Chemical substance... manganese strontium oxide (PMN P-00-1124; CAS No. 359427-90-0) is subject to reporting under this...

  7. Proper Management for Morbid Iatrogenic Retroperitoneal Barium Insufflation

    PubMed Central

    Vahedian-Ardakani, Jalal; Nazerani, Shahram; Saraee, Amir; Sarmast, Ali; Saraee, Ehsan

    2014-01-01

    A barium enema is a diagnostic and therapeutic procedure commonly used for colon and rectum problems. Rectal perforation with extensive intra- and/or extraperitoneal spillage of barium is a devastating complication of a barium enema that leads to a significant increase in patient mortality. Due to the low number of reported cases in recent scientific literature and the lack of experience with the management of these cases, we would like to present our treatment approach to a rare case of retroperitoneal contamination with barium, followed by its intraperitoneal involvement during a diagnostic barium enema. Our experience with long-term management of the patient and the good outcome will be depicted in this paper. PMID:25580416

  8. Barium Enhancement in NGC 6819 Blue Stragglers

    NASA Astrophysics Data System (ADS)

    Milliman, Katelyn; Mathieu, Robert D.; Schuler, Simon C.

    2015-01-01

    Possible formation pathways for blue straggler stars include mergers in hierarchical triple systems, stellar collisions during dynamical encounters, and mass transfer from a giant companion. Extensive work on the blue stragglers in the old open cluster NGC 188 (7 Gyr) has led to exciting discoveries including a binary secondary mass distribution peaked at 0.5 MSolar and the detection of three young white dwarf binary companions. These indicate that mass transfer from an asymptotic giant branch star is the dominant mechanism for blue straggler formation in open clusters. Such mass transfer events should pollute the surface abundance of the blue straggler with nucleosynthesis products from the evolved donor. The other formation pathways, mergers and collisions, are predicted to produce no such enhancements. In an effort to move beyond NGC 188 and into other open clusters we present the first results of a surface abundance study of the blue stragglers in the intermediate-aged open cluster NGC 6819 (2.5 Gyr) using the Hydra multi-object spectrograph on the WIYN 3.5 m telescope. This part of our study centers on the s-process element barium as a tracer of formation via mass transfer. We compare the blue straggler surface abundance of barium to that of a sample of main-sequence stars in NGC 6819 and find multiple blue stragglers with anomalous abundances. Surprising, most of the blue stragglers with barium anomalies show no radial-velocity evidence for a companion. We gratefully acknowledge funding from the National Science Foundation under grant AST- 0908082 and the Wisconsin Space Grant Consortium.

  9. Scattering lengths of calcium and barium isotopes

    E-print Network

    U. Dammalapati; L. Willmann; S. Knoop

    2011-10-25

    We have calculated the s-wave scattering length of all the even isotopes of calcium (Ca) and barium (Ba), in order to investigate the prospect of Bose-Einstein condensation (BEC). For Ca we have used an accurate molecular potential based on detailed spectroscopic data. Our calculations show that Ca does not provide other isotopes alternative to the recently Bose condensed 40Ca that suffers strong losses because of a very large scattering length. For Ba we show by using a model potential that the even isotopes cover a broad range of scattering lengths, opening the possibility of BEC for at least one of the isotopes.

  10. Scattering lengths of calcium and barium isotopes

    SciTech Connect

    Dammalapati, U.; Willmann, L.; Knoop, S.

    2011-11-15

    We have calculated the s-wave scattering length of all the even isotopes of calcium (Ca) and barium (Ba) in order to investigate the prospect of Bose-Einstein condensation (BEC). For Ca we have used an accurate molecular potential based on detailed spectroscopic data. Our calculations show that Ca does not provide other isotopes alternative to the recently Bose condensed {sup 40}Ca that suffers strong losses because of a very large scattering length. For Ba we show by using a model potential that the even isotopes cover a broad range of scattering lengths, opening the possibility of BEC for at least one of the isotopes.

  11. Short-cavity squeezing in barium

    NASA Technical Reports Server (NTRS)

    Hope, D. M.; Bachor, H-A.; Manson, P. J.; Mcclelland, D. E.

    1992-01-01

    Broadband phase sensitive noise and squeezing were experimentally observed in a system of barium atoms interacting with a single mode of a short optical cavity. Squeezing of 13 +/- 3 percent was observed. A maximum possible squeezing of 45 +/- 8 percent could be inferred for out experimental conditions, after correction for measured loss factors. Noise reductions below the quantum limit were found over a range of detection frequencies 60-170 MHz and were best for high cavity transmission and large optical depths. The amount of squeezing observed is consistent with theoretical predictions from a full quantum statistical model of the system.

  12. Europium-doped barium bromide iodide

    SciTech Connect

    Gundiah, Gautam; Hanrahan, Stephen M.; Hollander, Fredrick J.; Bourret-Courchesne, Edith D.

    2009-10-21

    Single crystals of Ba0.96Eu0.04BrI (barium europium bromide iodide) were grown by the Bridgman technique. The title compound adopts the ordered PbCl2 structure [Braekken (1932). Z. Kristallogr. 83, 222-282]. All atoms occupy the fourfold special positions (4c, site symmetry m) of the space group Pnma with a statistical distribution of Ba and Eu. They lie on the mirror planes, perpendicular to the b axis at y = +-0.25. Each cation is coordinated by nine anions in a tricapped trigonal prismatic arrangement.

  13. Barium dierbium(III) tetra-sulfide.

    PubMed

    Mesbah, Adel; Stojko, Wojciech; Ibers, James A

    2013-03-01

    Barium dierbium(III) tetra-sulfide, BaEr2S4, crystallizes with four formula units in the ortho-rhom-bic space group Pnma in the CaFe2O4 structure type. The asymmetric unit contains two Er, one Ba, and four S atoms, each with .m. site symmetry. The structure consists of channels formed by corner- and edge-sharing ErS6 octa-hedra in which Ba atoms reside. The resultant coordination of Ba is that of a bicapped trigonal prism. PMID:23476480

  14. Impact of glacial/interglacial changes in water column geochemistry on the diagenetic cycling of barium in Black Sea sediments

    NASA Astrophysics Data System (ADS)

    Kasten, S.; Henkel, S.; Mogollón, J. M.; Nöthen, K.; Franke, C.; Bogus, K.; Robin, E.; Bahr, A.; Blumenberg, M.; Pape, T.; Seifert, R.; Marz, C.; De Lange, G. J.

    2012-12-01

    Changes in depositional conditions and redox environment over time affect biogeochemical processes in the seabed and in this way control the variable and selective preservation, alteration and formation of various sediment constituents and attributes - including particulate organic matter, mineral assemblages and magnetic properties. As many of these solid-phase compounds are used as paleo-environmental tracers or stratigraphic tools an assessment of diagenetic influences on the sedimentary record is crucial for accurate environmental reconstructions. We present an integrated approach of pore-water and solid-phase geochemistry as well as transport reaction modeling for sediments of the Black Sea to assess the biogeochemical history of these deposits with particular emphasis on post-depositional redistribution of barium as a consequence of changes in water column geochemistry and redox (Henkel et al., 2012). High-resolution sedimentary records of major and minor elements (Al, Ba, Ca, Sr, Ti), total organic carbon (TOC), and profiles of pore-water constituents (SO42-, CH4, Ca2+, Ba2+, Mg2+, alkalinity) were obtained for two gravity cores (core 755, 501 m water depth and core 214, 1686 m water depth) from the northwestern Black Sea. The records were examined in order to gain insight into the cycling of Ba in anoxic marine sediments characterized by a shallow sulfate-methane transition (SMT) as well as the applicability of barite as a primary productivity proxy in such a setting. The Ba records are strongly overprinted by diagenetic barite (BaSO4) remobilization and precipitation; authigenic Ba enrichments were found at both sites at and slightly above the current SMT. Transport reaction modeling was applied to simulate the migration of the SMT during the changing geochemical conditions after the Holocene seawater intrusion into the Black Sea. Based on this, sediment intervals affected by diagenetic Ba redistribution were identified. Results reveal that the intense overprint of Ba and Baxs (Ba excess above detrital average) strongly limits its correlation to primary productivity. These findings have implications for other modern and ancient anoxic basins, such as sections covering the Oceanic Anoxic Events for which Ba is frequently used as a primary productivity indicator. Our study also demonstrates the limitations concerning the use of Baxs as a tracer for downward migrations of the SMT: due to high sedimentation rates at the investigated sites, diagenetic barite fronts are buried below the SMT within a relatively short period. Thus, "relict" barite fronts would only be preserved for a few thousands of years, if at all. References Henkel, S., Mogollón, J.M., Nöthen, K., Franke, C., Bogus, K., Robin, E., Bahr, A., Blumenberg, M., Pape, T., Seifert, R., März, C., de Lange, G.J., Kasten, S. (2012) Diagenetic barium cycling in Black Sea sediments - A case study for anoxic marine environments. Geochimica et Cosmochimica Acta, 88, 88-105.

  15. Hydrazine/Hydrazine sulfate

    Integrated Risk Information System (IRIS)

    Hydrazine / Hydrazine sulfate ; CASRN 302 - 01 - 2 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Non

  16. Aluminum Sulfate 18 Hydrate

    ERIC Educational Resources Information Center

    Young, Jay A.

    2004-01-01

    A chemical laboratory information profile (CLIP) of the chemical, aluminum sulfate 18 hydrate, is presented. The profile lists physical and harmful properties, exposure limits, reactivity risks, and symptoms of major exposure for the benefit of teachers and students using the chemical in the laboratory.

  17. Aqueous sulfate separation by crystallization of sulfate–water clusters

    DOE PAGESBeta

    Custelcean, Radu; Williams, Neil J.; Seipp, Charles A.

    2015-08-07

    An effective approach to separating sulfates from aqueous solutions is based on the crystallization of extended [SO4(H2O) 52-]n sulfate–water clusters with a bis(guanidinium) ligand. The ligand was generated in situ by hydrazone condensation in water, thus avoiding elaborate syntheses, tedious purifications, and organic solvents. Crystallization of sulfate–water clusters represents an alternative to the now established sulfate separation strategies that involve encapsulating the “naked” anion.

  18. Fluid seepage along the San Clemente Fault scarp: basin-wide impact on barium cycling

    E-print Network

    Huh, Chih-An

    Fluid seepage along the San Clemente Fault scarp: basin-wide impact on barium cycling Marta E present evidence that the barium released at cold seeps along the San Clemente Fault zone may significantly impact the geochemical budget of barium within the basin. Barium fluxes at seep localities

  19. Sulfate metabolism. I. Sulfate uptake and redistribution of acid rain sulfate by edible plants

    SciTech Connect

    Dallam, R.D.

    1987-03-23

    Sulfur is the major component of polluted air in industrialized societies. Atmospheric sulfur is converted to sulfuric acid through a series of chemical reactions which can eventually reenter many ecosystems. When edible plants are grown in soils containing varying amounts of sulfate, the roots take up and transport inorganic sulfate to the stems and leaves. The sulfate taken up by the roots and the amount transported to the stem and leaves was found to be a function of the concentration of sulfate in the soil. Inorganic sulfate taken up by a corn plant seedling can be rapidly converted to organic sulfate by the root system. Nine days after one of a pair of pea plants was inoculated with artificial acid rain sulfate (dilute H/sub 2//sup 35/SO/sub 4/) it was found that the sulfate was translocated not only in the inoculated plant, but also to the uninoculated pea plant in the same container. Also, when the leaves of a mature potato plant were inoculated with artificial acid rain sulfate it was found that the sulfate was translocated into the edible potatoes. Fractionation of the potatoes showed that most of the sulfate was water soluble of which 30% was inorganic sulfate and 70% was in the form of organic sulfur. One third of the non-water soluble translocated acid rain sulfate was equally divided between lipid and non-lipid organic sulfur of the potato. 9 references, 2 figures, 5 tables.

  20. Iron Reduction and Carbonate Precipitation by Shewanella oneidensis

    NASA Astrophysics Data System (ADS)

    Zeng, Z.; Tice, M. M.

    2011-12-01

    This study is to contribute to better understanding of how Archean microbes induced carbonate diagenesis in mats and stromatolites. Previous studies showed sulfate reduction, a common promoter of carbonate precipitation in modern mats[1], is likely to have been less effective in Archean mats in marine fluids lower in sulfate[2]. Alternatively, iron reduction produces far more alkalinity per unit carbon respired than sulfate reduction. Therefore, we hypothesize iron reduction can promote much more carbonate precipitation than sulfate reduction. Our study might also have some relevance to banded iron formation on which microbial iron reduction played a potential role[3]. To test our hypothesis, Shewanella oneidensis MR-1, a dissimilatory iron reducing bacterium will be cultured anaerobically (79%N2, 20%CO2 and 1%H2) in basal medium to trigger iron reduction. Lactate will be used as electron donor, and the electron acceptor will be fresh ferrihydrite. Culture medium will be added with various metal ions, such as Ca2+ and Mg2+, to obtain potential carbonate precipitate. Escherichia coli (with fumarate added as an electron acceptor) will be used to provide a comparison to live but non-iron- reduction cells. After 20 days incubation, precipitate will be collected, washed and identified by X-ray diffraction (XRD). Besides, iron reduction rate (ferrozine assay)[4], PH and amount of precipitate (carbonate and oxidize fractions)[5] will be measured over time to well understand how S. oneidensis drives carbonate precipitation.

  1. Do all barium stars have a white dwarf companion?

    NASA Technical Reports Server (NTRS)

    Dominy, J. F.; Lambert, D. L.

    1983-01-01

    International Ultraviolet Explorer short-wavelength, low-dispersion spectra were analyzed for four barium, two mild barium, and one R-type carbon star in order to test the hypothesis that the barium and related giants are produced by mass transfer from a companion now present as a white dwarf. An earlier tentative identification of a white dwarf companion to the mild barium star Zeta Cyg is confirmed. For the other stars, no ultraviolet excess attributable to a white dwarf is seen. Limits are set on the bolometric magnitude and age of a possible white dwarf companion. Since the barium stars do not have obvious progenitors among main-sequence and subgiant stars, mass transfer must be presumed to occur when the mass-gaining star is already on the giant branch. This restriction, and the white dwarf's minimum age, which is greater than 8 x 10 to the 8th yr, determined for several stars, effectively eliminates the hypothesis that mass transfer from an asymptotic giant branch star creates a barium star. Speculations are presented on alternative methods of producing a barium star in a binary system.

  2. Precipitation chemistry in central Amazonia

    NASA Technical Reports Server (NTRS)

    Andreae, M. O.; Talbot, R. W.; Berresheim, H.; Beecher, K. M.

    1990-01-01

    Rain samples from three sites in central Amazonia were collected over a period of 6 weeks during the 1987 wet season and analyzed for ionic species and dissolved organic carbon. A continuous record of precipitation chemistry and amount was obtained at two of these sites, which were free from local or regional pollution, for a time period of over 1 month. The volume-weighted mean concentrations of most species were found to be about a factor of 5 lower during the wet season compared with previous results from the dry season. Only sodium, potassium, and chloride showed similar concentrations in both seasons. When the seasonal difference in rainfall amount is taken into consideration, the deposition fluxes are only slightly lower for most species during the wet season than during the dry season, again with the exception of chloride, potassium, and sodium. Sodium and chloride are present in the same ratio as in sea salt; rapid advection of air masses of marine origin to the central Amazon Basin during the wet season may be responsible for the observed higher deposition flux of these species. Statistical analysis suggests that sulfate is, to a large extent, of marine (sea salt and biogenic) origin, but that long-range transport of combustion-derived aerosols also makes a significant contribution to sulfate and nitrate levels in Amazonian rain. Organic acid concentrations in rain were responsible for a large fraction of the observed precipitation acidity; their concentration was strongly influenced by gas/liquid interactions.

  3. Calcium sulfate crystallization along citrus root channels in a Florida soil exhibiting acid sulfate properties

    SciTech Connect

    Syslo, S.K.; Myhre, D.L.; Harris, W.G.

    1988-02-01

    The authors observed euhedral crystals in Manatee soil in a citrus grove in St. Lucie County, Florida. The material was identified as gypsum (CaSO/sub 4/ /times/ 2H/sub 2/O) using x-ray diffraction and infrared spectra. Photomicrography and scanning electron microscopy revealed that gypsum accumulated both in old root channels and within citrus root tissue of the Btg horizon. The subsurface horizons had elevated sulfate levels, a low initial pH, a drop (0.5 unit) in pH upon air-drying. Electrical conductivity paralleled the concentration of water-soluble sulfate. High levels of calcium and sulfate occurred for horizons above the water table. This accumulation is attributed to groundwater bearing these ions and subsequently discharging them to the overlying soil. Dead citrus roots appear to act as wicks to aid water transfer from lower to higher horizons. The roots and their empty channels provide spaces in which the gypsum can precipitate if the concentrations of calcium and sulfate in the evaporating groundwater exceed the solubility product of gypsum.

  4. A high-altitude barium radial injection experiment

    NASA Technical Reports Server (NTRS)

    Wescott, E. M.; Stenbaek-Nielsen, H. C.; Hallinan, T. J.; Deehr, C. S.; Romick, G. J.; Olson, J. V.; Roederer, J. G.; Sydora, R.

    1980-01-01

    A rocket launched from Poker Flat, Alaska, carried a new type of high-explosive barium shaped charge to 571 km, where detonation injected a thin disk of barium vapor with high velocity nearly perpendicular to the magnetic field. The TV images of the injection are spectacular, revealing three major regimes of expanding plasma which showed early instabilities in the neutral gas. The most unusual effect of the injection is a peculiar rayed barium-ion structure lying in the injection plane and centered on a 5 km 'black hole' surrounding the injection point. Preliminary electrostatic computer simulations show a similar rayed development.

  5. Extraperitoneal perforation of the rectum during barium enema.

    PubMed

    Rosenklint, A; Buemann, B; Hansen, P; Baden, H

    1975-01-01

    During barium enema, barium pentrated the rectum to the perirectal extraperitoneal tissue in six patients. Four of these died, and the two survivors have permanent colostomies. The incidence of this rare complication may be further reduced if barium enema is postponed after instrumentation of the rectum, the enema can not lifted more than one meter, the balloon not distended too much, the tip of the balloon catheter made very short, and the personnel in the radiological department made aware of the complication. The complication is probably best treated by prompt diverting colostomy, drainage of perirectal tissue, and antibiotics. PMID:1124343

  6. Proton conductivity of potassium doped barium zirconates

    SciTech Connect

    Xu Xiaoxiang; Tao Shanwen; Irvine, John T.S.

    2010-01-15

    Potassium doped barium zirconates have been synthesized by solid state reactions. It was found that the solubility limit of potassium on A-sites is between 5% and 10%. Introducing extra potassium leads to the formation of second phase or YSZ impurities. The water uptake of barium zirconates was increased even with 5% doping of potassium at the A-site. The sintering conditions and conductivity can be improved significantly by adding 1 wt% ZnO during material synthesis. The maximum solubility for yttrium at B-sites is around 15 at% after introducing 1 wt% zinc. The conductivity of Ba{sub 0.95}K{sub 0.05}Zr{sub 0.85}Y{sub 0.11}Zn{sub 0.04}O{sub 3-{delta}} at 600 deg. C is 2.2x10{sup -3} S/cm in wet 5% H{sub 2}. The activation energies for bulk and grain boundary are 0.29(2), 0.79(2) eV in wet 5% H{sub 2} and 0.31(1), 0.74(3) eV in dry 5% H{sub 2}. A power density of 7.7 mW/cm{sup 2} at 718 deg. C was observed when a 1 mm thick Ba{sub 0.95}K{sub 0.05}Zr{sub 0.85}Y{sub 0.11}Zn{sub 0.04}O{sub 3-{delta}} pellet was used as electrolyte and platinum electrodes. - Graphical abstract: Potassium doped barium zirconates have been synthesized by solid state reactions. It was found that the solubility limit of potassium on A-sites is between 5% and 10 %. The sintering conditions and conductivity can be improved significantly by adding 1 wt% ZnO during material synthesis. Five percent doping of potassium at A-site can double the total conductivity.

  7. Phased surgical treatment of barium enema-induced rectal injury and retention of barium in the pelvic floor space

    PubMed Central

    Yang, Xuefei; Xia, Ligang; Huang, Jun; Wang, Jianping

    2014-01-01

    Iatrogenic injuries caused by barium enema are rarely reported. Following a phased surgical protocol for up to one year, we have successfully treated a patient with rectal injury and severe infection of the pelvic floor space complicated with retention of large amounts of barium and vaginal fistula. In this article, the phased surgery planning for the treatment of rectal injury complicated with vaginal fistula is discussed in terms of the pros and cons, and the observed effect and evolution of barium retained in the pelvic floor space are described. PMID:25405155

  8. Large Flexoelectric Anisotropy in Paraelectric Barium Titanate.

    PubMed

    Narvaez, Jackeline; Saremi, Sahar; Hong, Jiawang; Stengel, Massimiliano; Catalan, Gustau

    2015-07-17

    The bending-induced polarization of barium titanate single crystals has been measured with an aim to elucidate the origin of the large difference between theoretically predicted and experimentally measured flexoelectricity in this material. The results indicate that part of the difference is due to polar regions (short-range order) that exist above T(C) and up to T*?200-225?°C. Above T*, however, the flexovoltage coefficient still shows an unexpectedly large anisotropy for a cubic material, with (001)-oriented crystals displaying 10 times more flexoelectricity than (111)-oriented crystals. Theoretical analysis shows that this anisotropy cannot be a bulk property, and we therefore interpret it as indirect evidence for the theoretically predicted but experimentally elusive contribution of surface piezoelectricity to macroscopic bending-induced polarization. PMID:26230825

  9. Theoretical isotope shifts in neutral barium

    E-print Network

    Nazé, Cédric; Godefroid, Michel

    2015-01-01

    The present work deals with a set of problems in isotope shifts of neutral barium spectral lines. Some well known transitions ($6s^2~^1S_0-6s6p~^{1,3}P^o_1$ and $6s^2~^1S_0-6p^2~^3P_0$) are first investigated. Values of the changes in the nuclear mean-square charge radius are deduced from the available experimental isotope shifts using our ab initio electronic factors. The three sets $\\{ \\delta\\langle r^2\\rangle^{A,A'}\\} $ obtained from these lines are consistent with each other. The combination of the available nuclear mean-square radii with our electronic factors for the $6s5d~^3D_{1,2} -6s6p~^{1}P^o_1$ transitions produces isotope shift values in conflict with the laser spectroscopy measurements of Dammalapati et al. (Eur. Phys. J. D 53, 1 (2009)).

  10. Calculated emission rates for barium releases in space

    NASA Technical Reports Server (NTRS)

    Stenbaek-Nielsen, H. C.

    1989-01-01

    The optical emissions from barium releases in space are caused by resonance and fluorescent scattering of sunlight. Emission rates for the dominant ion and neutral lines are calculated assuming the release to be optically thin and the barium to be in radiative equilibrium with the solar radiation. The solar spectrum has deep Fraunhofer absorption lines at the primary barium ion resonances. A velocity component toward or away from the sun will Doppler shift the emission lines relative to the absorption lines and the emission rates will increase many-fold over the rest value. The Doppler brightening is important in shaped charge or satellite releases where the barium is injected at high velocities. Emission rates as a function of velocity are calculated for the 4554, 4934, 5854, 6142 and 6497 A ion emission lines and the dominant neutral line at 5535 A. Results are presented for injection parallel to the ambient magnetic field, B, and for injection at an angle to B.

  11. Upper gastrointestinal barium evaluation of duodenal pathology: A pictorial review

    PubMed Central

    Gupta, Pankaj; Debi, Uma; Sinha, Saroj Kant; Prasad, Kaushal Kishor

    2014-01-01

    Like other parts of the gastrointestinal tract (GIT), duodenum is subject to a variety of lesions both congenital and acquired. However, unlike other parts of the GIT viz. esophagus, rest of the small intestine and large intestine, barium evaluation of duodenal lesions is technically more challenging and hence not frequently reported. With significant advances in computed tomography technology, a thorough evaluation including intraluminal, mural and extramural is feasible in a single non-invasive examination. Notwithstanding, barium evaluation still remains the initial and sometimes the only imaging study in several parts of the world. Hence, a thorough acquaintance with the morphology of various duodenal lesions on upper gastrointestinal barium examination is essential in guiding further evaluation. We reviewed our experience with various common and uncommon barium findings in duodenal abnormalities. PMID:25170399

  12. Evolution of structure in the PLACES barium clouds

    NASA Astrophysics Data System (ADS)

    Simons, D. J.; Lebeda, C. F.; Pongratz, M. B.; Fitzgerald, T. J.; Dupre, R. R.

    1984-02-01

    The PLACES (Position Location and Communication Effects Simulations) experiment is discussed. Intensified optical instruments are used to examine the barium ion and neutral resonance fluorescence light from the four barium ionospheric thermite releases. The effects of structured ionospheric plasmas on transionospheric radio communication lines are determined. As part of this experiment, it was necessary to characterize the evolution of the structure (striations) in the barium ionospheric plasma. The motivation for using barium to simulate these effects is examined. The theoretical and empirical basis for using optical diagnostics for deriving the electron column content of the ion clouds is discussed. The time evolution of the power spectral density (PSD) of striations for the electron column density perpendicular to the magnetic field is derived for the two clouds.

  13. Study of the photovoltaic effect in thin film barium titanate

    NASA Technical Reports Server (NTRS)

    Grannemann, W. W.; Dharmadhikari, V. S.

    1983-01-01

    The feasibility of making non-volatile digital memory devices of barium titanate, BaTiO3, that are integrated onto a silicon substrate with the required ferroelectric film produced by processing, compatible with silicon technology was examined.

  14. Polymorphic change from vaterite to aragonite under influence of sulfate: The "morning star" habit

    NASA Astrophysics Data System (ADS)

    Wagterveld, R. M.; Yu, M.; Miedema, H.; Witkamp, G. J.

    2014-02-01

    The presence of sulfate in reverse osmosis drinking water concentrate and its effect on calcium carbonate precipitation was studied, notably the overall kinetics of CaCO3 formation and the types of polymorphs formed. CaCO3 formation slows down with increasing sulfate concentration and the preferential polymorph shifts from vaterite to aragonite with increasing sulfate concentration. With this polymorphic change, a new combined habit is observed where aragonite spikes grow on top of vaterite ("morning star" habit). The presence of a moderate magnesium concentration results in the shift of vaterite to aragonite at relatively low sulfate concentrations; where sulfate and magnesium appear to have an additive effect. Without magnesium, spikes on top of vaterite were also observed, but only at relatively high sulfate concentration. Without the presence of magnesium, single crystals of aragonite were not found.

  15. Synthesis, photoluminescence and magnetic properties of barium vanadate nanoflowers

    SciTech Connect

    Xu, Jing; Chongqing University of Science and Technology, Chongqing 401331 ; Hu, Chenguo; Xi, Yi; Peng, Chen; Wan, Buyong; He, Xiaoshan

    2011-06-15

    Graphical abstract: The flower-shaped barium vanadate was obtained for the first time. The photoluminescence and magnetic properties of the barium vanadate nanoflowers were investigated at room temperature. Research highlights: {yields} In the paper, the flower-shaped barium vanadate were obtained for the first time. The CHM method used here is new and simple for preparation of barium vanadate. {yields} The photoluminescence and magnetic properties of the barium vanadate nanoflowers were investigated at room temperature. The strong bluish-green emission was observed. {yields} The ferromagnetic behavior of the barium vanadate nanoflowers was found with saturation magnetization of about 83.50 x 10{sup -3} emu/g, coercivity of 18.89 Oe and remnant magnetization of 4.63 x 10{sup -3} emu/g. {yields} The mechanisms of PL and magnetic property of barium vanadate nanoflowers have been discussed. -- Abstract: The flower-shaped barium vanadate has been obtained by the composite hydroxide mediated (CHM) method from V{sub 2}O{sub 5} and BaCl{sub 2} at 200 {sup o}C for 13 h. XRD and XPS spectrum of the as-synthesized sample indicate it is hexagonal Ba{sub 3}V{sub 2}O{sub 8} with small amount of Ba{sub 3}VO{sub 4.8} coexistence. Scan electron microscope and transmission electron microscope display that the flower-shaped crystals are composed of nanosheets with thickness of {approx}20 nm. The UV-visible spectrum shows that the barium vanadate sample has two optical gaps (3.85 eV and 3.12 eV). Photoluminescence spectrum of the barium vanadate flowers exhibits a visible light emission centered at 492 and 525 nm which might be attributed to VO{sub 4} tetrahedron with T{sub d} symmetry in Ba{sub 3}V{sub 2}O{sub 8}. The ferromagnetic behavior of the barium vanadate nanoflowers has been found with saturation magnetization of about 83.50 x 10{sup -3} emu/g, coercivity of 18.89 Oe and remnant magnetization of 4.63 x 10{sup -3} emu/g, which is mainly due to the presence of a non-orthovanadate phase with spin S = 1/2.

  16. Solar eclipse sign of intussusception on barium enema.

    PubMed

    Raveenthiran, V

    2002-01-01

    The colographic appearance of intussusception is variously described as a claw sign, pincer defect, shouldering effect, and coiled-spring pattern. This report adds a new radiographic sign to the list. An end-on view of an intussusception on barium enema shows a ring of contrast resembling a solar eclipse. Familiarity with this bizarre appearance is desirable, lest it may be mistaken for spillage of barium due to a colonic perforation. PMID:11793074

  17. 'Skidding' of the CRRES G-9 barium release

    NASA Technical Reports Server (NTRS)

    Huba, J. D.; Mitchell, H. G.; Fedder, J. A.; Bernhardt, P. A.

    1992-01-01

    A simulation study and experimental data of the CRRES G-9 ionospheric barium release are presented. The simulation study is based on a 2D electrostatic code that incorporates time-dependent coupling to the background plasma. It is shown that the densest portion of the barium ion cloud 'skids' about 15 km within the first three seconds following the release, consistent with the optical data analyses.

  18. A search for technetium (Tc II) in barium stars

    NASA Technical Reports Server (NTRS)

    Little-Marenin, Irene R.; Little, Stephen J.

    1987-01-01

    The authors searched without success for the lines of Tc II at 2647.02, 2610.00 and 2543.24 A in IUE spectra of the barium stars HR 5058, Omicron Vir, and Zeta Cap. The lack of Tc II implies that the observed s-process enhancements were produced more than half a million years ago and supports the suggestion that the spectral peculiarities of barium stars are probably related to the binary nature of the stars.

  19. Aqueous sulfate separation by crystallization of sulfate–water clusters

    SciTech Connect

    Custelcean, Radu; Williams, Neil J.; Seipp, Charles A.

    2015-08-07

    An effective approach to separating sulfates from aqueous solutions is based on the crystallization of extended [SO4(H2O) 52-]n sulfate–water clusters with a bis(guanidinium) ligand. The ligand was generated in situ by hydrazone condensation in water, thus avoiding elaborate syntheses, tedious purifications, and organic solvents. Crystallization of sulfate–water clusters represents an alternative to the now established sulfate separation strategies that involve encapsulating the “naked” anion.

  20. Barium recovery by crystallization in a fluidized-bed reactor: effects of pH, Ba/P molar ratio and seed.

    PubMed

    Su, Chia-Chi; Reano, Resmond L; Dalida, Maria Lourdes P; Lu, Ming-Chun

    2014-06-01

    The effects of process conditions, including upward velocity inside the column, the amount of added seed and seed size, the pH value of the precipitant or the phosphate stream and the Ba/P molar ratio in a fluidized-bed reactor (FBR) were studied with a view to producing BaHPO? crystals of significant size and maximize the removal of barium. XRD were used to identify the products that were collected from the FBR. Experimental results show that an upward velocity of 48 cmmin(-1) produced the largest BaHPO? crystals with a size of around 0.84-1.0mm. The addition of seed crystals has no effect on barium removal. The use of a seed of a size in the ranges unseeded<0.149-0.29 mm<0.149 mm<0.29-0.42 mm produced increasing amounts of increasingly large crystals. The largest BaHPO? crystals were obtained at pH 8.4-8.8 with a Ba/P molar ratio of 1.0. In the homogeneous and heterogeneous processes, around 98% of barium was removed at pH 8.4-8.6 and [Ba]/[P]=1.0. The XRD results show that a significant amount of barium phosphate (Ba?(PO?)?) was obtained at pH 11. The compounds BaHPO? and BaO were present at a pH of below 10. PMID:24462085

  1. Remediation of acid mine drainage with sulfate reducing bacteria

    SciTech Connect

    Hauri, J.F.; Schaider, L.A.

    2009-02-15

    Sulfate reducing bacteria have been shown to be effective at treating acid mine drainage through sulfide production and subsequent precipitation of metal sulfides. In this laboratory experiment for undergraduate environmental chemistry courses, students design and implement a set of bioreactors to remediate acid mine drainage and explain observed changes in dissolved metal concentrations and pH. Using synthetic acid mine drainage and combinations of inputs, students monitor their bioreactors for decreases in dissolved copper and iron concentrations.

  2. Sulfate in acid rain data - do the patterns make sense?

    SciTech Connect

    Stensland, G.J.

    1997-12-31

    A high quality national record of precipitation chemistry is being collected through the operation of the National Atmospheric Deposition Program/National Trends Network (NADP/NTN). This network began in 1978 with less than 20 sites and by the mid 1980`s had grown to about 200 sites which is about the number of sites currently in operation. Lynch et al. have been reporting time trend results for this data, with their most recent analysis showing that sulfate in NADP/NTN decreased dramatically in 1995 which agrees with the substantial decrease in sulfur dioxide emissions. The various network data available before NADP/NTN have been reported to have a variety of problems, especially related to the effect on pH of the elevated levels of base cations. The sulfate and nitrate data may be more useable. This paper reassesses the sulfate data available from the Junge network to see if these data can be used to extend the comparison of sulfate in precipitation and sulfur dioxide emissions back to the mid 1950`s.

  3. High H? ionic conductivity in barium hydride.

    PubMed

    Verbraeken, Maarten C; Cheung, Chaksum; Suard, Emmanuelle; Irvine, John T S

    2015-01-01

    With hydrogen being seen as a key renewable energy vector, the search for materials exhibiting fast hydrogen transport becomes ever more important. Not only do hydrogen storage materials require high mobility of hydrogen in the solid state, but the efficiency of electrochemical devices is also largely determined by fast ionic transport. Although the heavy alkaline-earth hydrides are of limited interest for their hydrogen storage potential, owing to low gravimetric densities, their ionic nature may prove useful in new electrochemical applications, especially as an ionically conducting electrolyte material. Here we show that barium hydride shows fast pure ionic transport of hydride ions (H(-)) in the high-temperature, high-symmetry phase. Although some conductivity studies have been reported on related materials previously, the nature of the charge carriers has not been determined. BaH2 gives rise to hydride ion conductivity of 0.2 S cm(-1) at 630 °C. This is an order of magnitude larger than that of state-of-the-art proton-conducting perovskites or oxide ion conductors at this temperature. These results suggest that the alkaline-earth hydrides form an important new family of materials, with potential use in a number of applications, such as separation membranes, electrochemical reactors and so on. PMID:25485988

  4. High H- ionic conductivity in barium hydride

    NASA Astrophysics Data System (ADS)

    Verbraeken, Maarten C.; Cheung, Chaksum; Suard, Emmanuelle; Irvine, John T. S.

    2015-01-01

    With hydrogen being seen as a key renewable energy vector, the search for materials exhibiting fast hydrogen transport becomes ever more important. Not only do hydrogen storage materials require high mobility of hydrogen in the solid state, but the efficiency of electrochemical devices is also largely determined by fast ionic transport. Although the heavy alkaline-earth hydrides are of limited interest for their hydrogen storage potential, owing to low gravimetric densities, their ionic nature may prove useful in new electrochemical applications, especially as an ionically conducting electrolyte material. Here we show that barium hydride shows fast pure ionic transport of hydride ions (H-) in the high-temperature, high-symmetry phase. Although some conductivity studies have been reported on related materials previously, the nature of the charge carriers has not been determined. BaH2 gives rise to hydride ion conductivity of 0.2 S cm-1 at 630 °C. This is an order of magnitude larger than that of state-of-the-art proton-conducting perovskites or oxide ion conductors at this temperature. These results suggest that the alkaline-earth hydrides form an important new family of materials, with potential use in a number of applications, such as separation membranes, electrochemical reactors and so on.

  5. Prospects for Barium Tagging in Gaseous Xenon

    SciTech Connect

    Sinclair, D.; Rollin, E.; Smith, J.; Mommers, A.; Ackerman, N.; Aharmim, B.; Auger, M.; Barbeau, P.S.; Benitez-Medina, C.; Breidenbach, M.; Burenkov, A.; Cook, S.; Coppens, A.; Daniels, T.; DeVoe, R.; Dobi, A.; Dolinski, M.J.; Donato, K.; Fairbank, W., Jr.; Farine, J.; Giroux, G.; /Bern U., LHEP /Carleton U. /Stanford U., Phys. Dept. /Carleton U. /Laurentian U. /Carleton U. /SLAC /Indiana U. /Indiana U., CEEM /Korea U. /Stanford U., Phys. Dept. /SLAC /Alabama U. /Colorado State U. /Stanford U., Phys. Dept. /Alabama U. /SLAC /Stanford U., Phys. Dept. /Alabama U. /Massachusetts U., Amherst /SLAC /Alabama U. /SLAC /Maryland U. /Moscow, ITEP /Stanford U., Phys. Dept. /Maryland U. /Bern U., LHEP /Laurentian U. /SLAC /Maryland U.

    2012-05-03

    Tagging events with the coincident detection of a barium ion would greatly reduce the background for a neutrino-less double beta decay search in xenon. This paper describes progress towards realizing this goal. It outlines a source that can produce large quantities of Ba++ in gas, shows that this can be extracted to vacuum, and demonstrates a mechanism by which the Ba++ can be efficiently converted to Ba+ as required for laser identification. It is clear from this study that electrospray is a convenient mechanism for producing Ba++ is gas at atmospheric pressure. It is likely that the source will perform just as effectively at higher pressures. Even though the source region has water vapour and methanol vapour at the 0.3% level, there is no evidence for molecular formation. The use of TEA offers an effective method to achieve the charge state conversion. The overall design of the ion extraction from high pressure to vacuum is very similar to the scheme proposed for the final detector and this appears to work well although the efficiency is not yet determined.

  6. Determination of trace elements in triglycine sulfate solutions

    NASA Technical Reports Server (NTRS)

    Tadros, Shawky H.

    1993-01-01

    Ten elements were divided into 2 groups. The elements in the first group included iron, nickel, chromium, manganese, copper, and gold. The elements in the second group included zinc, cobalt, lead, cadmium, and gold. Five ppm of each element in each group was spiked in a 1 percent triglycine sulfate (TGS) solution. Glycine was removed with 1-naphthyl isocyanate in ether medium. The glycine derivative 1-naphthyl isocyanate glycine was removed by filtration, and the filtrates were analyzed for the different elements. Analysis of these elements was performed by using the 5100 Perkin-Elmer Atomic Absorption Spectrophotometer. The result of these experiments was the observation that there was a decrease in the concentration of chromium and gold, which was interpreted to be due to the chelation of these elements by the derivative 1-naphthyl isocyanate glycine. Further research is needed to determine the concentration of other elements in triglycine sulfate (TGS) solutions. These elements will include lithium, sodium, rubidium, magnesium, calcium, strontium, barium, aluminum, and silicon. These are the most likely elements to be found in the sulfuric acid used in manufacturing the TGS crystal. Moreover, we will extend our research to investigate the structural formula of the violet colored chelated compounds, which had been formed by interaction of the derivative 1-naphthyl isocyanate glycine with the different elements, such as gold, chromium.

  7. Natural or anthropogenic? On the origin of atmospheric sulfate deposition in the Andes of southeastern Ecuador

    NASA Astrophysics Data System (ADS)

    Makowski Giannoni, S.; Rollenbeck, R.; Trachte, K.; Bendix, J.

    2014-10-01

    Atmospheric sulfur deposition above certain limits can represent a threat to tropical forests, causing nutrient imbalances and mobilizing toxic elements that impact biodiversity and forest productivity. Atmospheric sources of sulfur deposited by precipitation have been roughly identified in only a few lowland tropical forests. Even scarcer are studies of this type in tropical mountain forests, many of them mega-diversity hotspots and especially vulnerable to acidic deposition. In these places, the topographic complexity and related streamflow conditions affect the origin, type, and intensity of deposition. Furthermore, in regions with a variety of natural and anthropogenic sulfur sources, like active volcanoes and biomass burning, no source emission data has been used for determining the contribution of each source to the deposition. The main goal of the current study is to evaluate sulfate (SO4- deposition by rain and occult precipitation at two topographic locations in a tropical mountain forest of southern Ecuador, and to trace back the deposition to possible emission sources applying back-trajectory modeling. To link upwind natural (volcanic) and anthropogenic (urban/industrial and biomass-burning) sulfur emissions and observed sulfate deposition, we employed state-of-the-art inventory and satellite data, including volcanic passive degassing as well. We conclude that biomass-burning sources generally dominate sulfate deposition at the evaluated sites. Minor sulfate transport occurs during the shifting of the predominant winds to the north and west. Occult precipitation sulfate deposition and likely rain sulfate deposition are mainly linked to biomass-burning emissions from the Amazon lowlands. Volcanic and anthropogenic emissions from the north and west contribute to occult precipitation sulfate deposition at the mountain crest Cerro del Consuelo meteorological station and to rain-deposited sulfate at the upriver mountain pass El Tiro meteorological station.

  8. Natural or anthropogenic? On the origin of atmospheric sulfate deposition in the Andes of southeastern Ecuador

    NASA Astrophysics Data System (ADS)

    Makowski Giannoni, S.; Rollenbeck, R.; Trachte, K.; Bendix, J.

    2014-05-01

    Atmospheric sulfur deposition above certain limits can represent a threat to tropical forests, causing nutrient imbalances and mobilizing toxic elements that impact biodiversity and forest productivity. Atmospheric sources of sulfur deposited by precipitation have being roughly identified in only a few lowland tropical forests. Even scarcer are these type of studies in tropical mountain forests, many of them megadiversity hotspots and especially vulnerable to acidic deposition. Here, the topographic complexity and related streamflow condition the origin, type, and intensity of deposition. Furthermore, in regions with a variety of natural and anthropogenic sulfur sources, like active volcanoes and biomass-burning, no source-emission data has been used for determining the contribution of each of them to the deposition. The main goal of the current study is to evaluate sulfate (SO4-) deposition by rain and occult precipitation at two topographic locations in a tropical mountain forest of southern Ecuador, and to trace back the deposition to possible emission sources applying back trajectory modeling. To link upwind natural (volcanic) and anthropogenic (urban/industrial and biomass-burning) sulfur emissions and observed sulfate deposition, we employed state of the art inventory and satellite data, including volcanic passive degassing as well. We conclude that biomass-burning sources generally dominate sulfate deposition at the evaluated sites. Minor sulfate transport occurs during the shifting of the predominant winds to the north and west. Occult precipitation sulfate deposition and likely rain sulfate deposition are mainly linked to biomass-burning emissions from the Amazon lowlands. Volcanic and anthropogenic emissions from the north and west contribute to occult precipitation sulfate deposition at the mountain crest Cerro del Consuelo meteorological station and to rain-deposited sulfate at the upriver mountain-pass El Tiro meteorological station.

  9. Millimeter wave phase shifter based on ferromagnetic resonance in a hexagonal barium ferrite thin film

    E-print Network

    Millimeter wave phase shifter based on ferromagnetic resonance in a hexagonal barium ferrite thin of an M-type barium ferrite BaM thin film prepared by pulsed laser deposition and a coplanar waveguide

  10. Tracking Phaselock Loop Characteristics with a VCO Using a Barium Strontium Titanate (BST)

    E-print Network

    Tracking Phaselock Loop Characteristics with a VCO Using a Barium Strontium Titanate (BST) Thin University, Raleigh, NC-27695-7919,USA, Ph: +1-919-767-3277, Email: avictor@harris.com Abstract -- Barium

  11. Cooling laser system for quantum computing with barium-137 ions Tom Chartrand

    E-print Network

    Blinov, Boris

    Cooling laser system for quantum computing with barium-137 ions Tom Chartrand Department of Physics for essentially any application. We have been trapping 137-barium with this end in mind. The odd isotope has

  12. Barium Depletion in the NSTAR Discharge Cathode After 30,000 Hours of Operation

    NASA Technical Reports Server (NTRS)

    Polk, James E.; Capece, Angela M.; Mikellides, Ioannis G.; Katz, Ira

    2010-01-01

    Dispenser hollow cathodes rely on a consumable supply of barium released by impregnant materials in the pores of a tungsten matrix to maintain a low work function surface. Examinations of cathode inserts from long duration ion engine tests show deposits of tungsten at the downstream end that appear to block the flow of barium from the interior. In addition, a numerical model of barium transport in the insert plasma indicates that the barium partial pressure in the insert may exceed the equilibrium vapor pressure of the dominant barium-producing reaction, and it was postulated previously that this would suppress barium loss in the upstream part of the insert. New measurements of the depth of barium depletion from a cathode insert operated for 30,352 hours reveal that barium loss is confined to a narrow region near the downstream end, confirming this hypothesis.

  13. Rocket having barium release system to create ion clouds in the upper atmosphere

    NASA Technical Reports Server (NTRS)

    Lewis, B. W.; Stokes, C. S.; Smith, E. W.; Murphy, W. J. (inventors)

    1974-01-01

    A chemical system for releasing a good yield of free barium atoms and barium ions to create ion clouds in the upper atmosphere and interplanetary space for the study of the geophysical properties of the medium is presented.

  14. Pyroelectric properties of barium strontium titanate films: Effect of thermal M. W. Cole,2

    E-print Network

    Alpay, S. Pamir

    Pyroelectric properties of barium strontium titanate films: Effect of thermal stresses J. Zhang,1 M pyroelectric properties of 001 -textured polycrystalline barium strontium titanate BaxSr1-xTiO3, BST films

  15. Enhanced dielectric properties from barium strontium titanate films with strontium titanate buffer layers

    E-print Network

    Alpay, S. Pamir

    Enhanced dielectric properties from barium strontium titanate films with strontium titanate buffer in their PE state. One of the leading material candidates for tunable materials is barium strontium titanate

  16. Acceleration of barium ions near 8000 km above an aurora

    NASA Technical Reports Server (NTRS)

    Stenbaek-Nielsen, H. C.; Hallinan, T. J.; Wescott, E. M.; Foeppl, H.

    1984-01-01

    A barium shaped charge, named Limerick, was released from a rocket launched from Poker Flat Research Range, Alaska, on March 30, 1982, at 1033 UT. The release took place in a small auroral breakup. The jet of ionized barium reached an altitude of 8100 km 14.5 min after release, indicating that there were no parallel electric fields below this altitude. At 8100 km the jet appeared to stop. Analysis shows that the barium at this altitude was effectively removed from the tip. It is concluded that the barium was actually accelerated upward, resulting in a large decrease in the line-of-sight density and hence the optical intensity. The parallel electric potential in the acceleration region must have been greater than 1 kV over an altitude interval of less than 200 km. The acceleration region, although presumably auroral in origin, did not seem to be related to individual auroral structures, but appeared to be a large-scale horizontal structure. The perpendicular electric field below, as deduced from the drift of the barium, was temporally and spatially very uniform and showed no variation related to individual auroral structures passing through.

  17. Process of precipitating zirconium or hafnium from spent pickling solutions

    SciTech Connect

    Aguilar, C.L.; Walker, R.G.

    1991-12-31

    This patent describes a process for regenerating a spent, fluoride-containing pickle solution used in the pickling of zirconium or hafnium metal or their alloys. It comprises adding to the spent pickle solution a sufficient amount of sodium sulfate to precipitate sodium zirconium or hafnium fluoride.

  18. Characterization of Jarosite Formed upon Bacterial Oxidation of Ferrous Sulfate in a Packed-Bed Reactor †

    PubMed Central

    Grishin, Sergei I.; Bigham, Jerry M.; Tuovinen, Olli H.

    1988-01-01

    A packed-bed bioreactor with activated-carbon particles as a carrier matrix material inoculated with Thiobacillus ferrooxidans was operated at a pH of 1.35 to 1.5 to convert ferrous sulfate to ferric sulfate. Despite the low operating pH, trace amounts of precipitates were produced in both the reactor and the oxidized effluent. X-ray diffraction and chemical analyses indicated that the precipitates were well-ordered potassium jarosite. The chemical analyses also revealed a relative deficiency of Fe and an excess of S in the reactor sample compared with the theoretical composition of potassium jarosite. Images PMID:16347799

  19. Ion Exchange Studies for Removal of Sulfate from Hanford Tank Waste Envelope C (241-AN-107) Using SuperLig 655 Resin

    SciTech Connect

    DE Kurath; JR Bontha; DL Blanchard; SK Fiskum; BM Rapko

    2000-08-23

    BNFL Inc. is evaluating various pretreatment technologies to mitigate the impacts of sulfate on the LAW vitrification system. One pretreatment technology for separating sulfate from LAW solutions involves the use of SuperLig{reg_sign} 655 (SL-655), a proprietary ion exchange material developed and supplied by IBC Advanced Technologies, Inc., American Fork, UT. This report describes testing of SL-655 with diluted ([Na] {approximately} 5 M) waste from Hanford Tank 241-AN-107 at Battelle, Pacific Northwest Division. Batch contact studies were conducted from 4 to 96 hours to determine the sulfate distribution coefficient and reaction kinetics. A small-scale ion exchange column test was conducted to evaluate sulfate removal, loading, breakthrough, and elution from the SL-655. In all of these tests, an archived 241-AN-107 tank waste sample (pretreated to remove Cs, Sr, and transuranics elements) was used. The experimental details and results are described in this report. Under the test conditions, SL-655 was found to have no significant ion exchange affinity for sulfate in this matrix. The batch contact study resulted in no measurable difference in the aqueous sulfate concentration following resin contact (K{sub d} {approximately} 0). The column test also demonstrated SL-655 had no practical affinity for sulfate in the tested matrix. Within experimental error, the sulfate concentration in the column effluent was equal to the concentration in the feed after passing 3 bed volumes of sample through the columns. Furthermore, some, if not all, of the decreased sulfate concentration in these first three column volumes of effluent can be ascribed to mixing and dilution of the 241-AN-107 feed with the interstitial liquid present in the column at the start of the loading cycle. Finally, ICP-AES measurements on the eluate solutions showed the presence of barium as soon as contact with the feed solution is completed. Barium is a metal not detected in the feed solution. Should the loss of barium be correlated with the resin's ability to selectively complex sulfate, then maintaining even the current limited resin characteristics for sulfate complexation over multiple cycles becomes questionable.

  20. Relation of precipitation quality to storm type, and deposition of dissolved chemical constituents from precipitation in Massachusetts, 1983-85

    USGS Publications Warehouse

    Gay, F.B.; Melching, C.S.

    1995-01-01

    Precipitation samples were collected for 83 storms at a rural inland site in Princeton, Mass., and 73 storms at a rural coastal site in Truro, Mass., to examine the quality of precipitation from storms and relate quality to three storm types (oceanic cyclone, continental cyclone, and cold front). At the inland site, Princeton, ranked-means of precipitation depth, storm duration, specific conductance, and concentrations and loads of hydrogen, sulfate, aluminum, bromide, and copper ions were affected by storm type. At the coastal site, Truro, ranked means of precipitation depth, storm duration, and concentrations and loads of calcium, chloride, magnesium, potassium, and sodium ions were affected by storm type. Precipitation chemistry at the coastal site was 85 percent oceanic in orgin, whereas precipitation 72 kilometers inland was 60 percent hydrogen, nitrate, and sulfate ions, reflecting fossil-fuel combustion. Concentrations and loads for specific conductance and 9 chemical constituents on an annual and seasonal basis were determined from National Atmospheric Deposition Program data for spring 1983 through winter 1985 at Quabbin (rural, inland), Waltham (suburban, inland) and Truro (rural, coastal), Massachusetts. Concentrations of magnesium, potassium, sodium, and chloride concentrations were highest at the coast and much lower inland, with very little difference between Waltham and Quabbin. Loads of ammonium, nitrate, sulfate, and hydrogen are highest at Quabbin and are about equal at Waltham and Truro. About twice as much nitrate and hydrogen and about 35 percent more sulfate is deposited at Quabbin than at Waltham or Truro; this pattern indicates that the interior of Massachusetts receives more acidic precipitation than do the eastern or the coastal areas of Massachusetts.

  1. Compact high power barium nitrite crystal-based Raman laser at 1197 nm

    E-print Network

    Cheng, Ji-Xin

    Compact high power barium nitrite crystal-based Raman laser at 1197 nm for photoacoustic imaging of fat Rui Li Mikhail N. Slipchenko Pu Wang Ji-Xin Cheng #12;Compact high power barium nitrite crystal such a barrier, we demonstrate the construction and use of a com- pact, barium nitrite crystal-based Raman laser

  2. 40 CFR 721.10010 - Barium manganese oxide (BaMnO3).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Barium manganese oxide (BaMnO3). 721... Substances § 721.10010 Barium manganese oxide (BaMnO3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as barium manganese oxide (BaMnO3) (PMN...

  3. Effect of Microwave Frequency on Hydrothermal Synthesis of Nanocrystalline Tetragonal Barium Titanate

    E-print Network

    Dutta, Prabir K.

    Effect of Microwave Frequency on Hydrothermal Synthesis of Nanocrystalline Tetragonal Barium, 2007; ReVised Manuscript ReceiVed: April 29, 2008 Nanocrystalline tetragonal barium titanate (BaTiO3. The dependence of properties of barium titanate on microwave frequency could be due to different transverse

  4. Single-Crystalline Barium Titanate By Jeffrey J. Urban, Jonathan E. Spanier, Lian Ouyang,

    E-print Network

    Walsworth, Ronald L.

    Single-Crystalline Barium Titanate Nanowires By Jeffrey J. Urban, Jonathan E. Spanier, Lian Ouyang composed of barium titanate (BaTiO3), a prototypical displacive ferroelectric material[14,15] that yields-volatile memory devices with an integration density approaching 1 terabit cm±2 . 2. Synthesis of Barium Titanate

  5. Phase associations of barium in marine sediments Meagan Eagle Gonneea *, Adina Paytan 1

    E-print Network

    Paytan, Adina

    Phase associations of barium in marine sediments Meagan Eagle Gonneea *, Adina Paytan 1 Department 2006 Abstract Barium (Ba) is associated with various phases in marine sediments, including carbonates-export productivity. D 2005 Elsevier B.V. All rights reserved. Keywords: Barium; Barite; Marine sediment; Sedimentary

  6. 40 CFR 721.10010 - Barium manganese oxide (BaMnO3).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Barium manganese oxide (BaMnO3). 721... Substances § 721.10010 Barium manganese oxide (BaMnO3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as barium manganese oxide (BaMnO3) (PMN...

  7. Nanoscale Patterning of Barium Titanate on Block Tu Lee,, Nan Yao, and Ilhan A. Aksay*,,

    E-print Network

    Aksay, Ilhan A.

    Nanoscale Patterning of Barium Titanate on Block Copolymers Tu Lee,, Nan Yao, and Ilhan A. Aksay of polystyrene-polybutadiene-polystyrene (Kraton D1102) has been used to pattern barium titanate precursor on the unsaturated carbon bonds in the polybutadiene matrix with antistereochemistry. Anchoring the barium titanate

  8. CORRELATED STRONTIUM AND BARIUM ISOTOPIC COMPOSITIONS OF ACID-CLEANED SINGLE MAINSTREAM SILICON CARBIDES FROM MURCHISON

    E-print Network

    CORRELATED STRONTIUM AND BARIUM ISOTOPIC COMPOSITIONS OF ACID-CLEANED SINGLE MAINSTREAM SILICON April 7 ABSTRACT We present strontium, barium, carbon, and silicon isotopic compositions of 61 acid effective in removing both strontium and barium contamination. For the first time, by using correlated 88 Sr

  9. The enhanced and optimal piezoelectric coefficients in single crystalline barium titanate with engineered domain configurations

    E-print Network

    Li, Jiangyu

    The enhanced and optimal piezoelectric coefficients in single crystalline barium titanate the effective electromechanical moduli of tetragonal barium titanate poled along 111 direction, where that poling along 111 direction does not lead to the optimal domain configuration, since barium titanate poled

  10. 40 CFR 721.10010 - Barium manganese oxide (BaMnO3).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Barium manganese oxide (BaMnO3). 721... Substances § 721.10010 Barium manganese oxide (BaMnO3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as barium manganese oxide (BaMnO3) (PMN...

  11. Structure evolution and dielectric behavior of polystyrene-capped barium titanate nanoparticles

    E-print Network

    Lin, Zhiqun

    Structure evolution and dielectric behavior of polystyrene-capped barium titanate nanoparticles H35600g Polystyrene-capped barium titanate (BaTiO3) nanoparticles with sizes of 11 nm and 27 nm were nanocrystals. 1. Introduction Barium titanate (BaTiO3), one of the most commonly used perovskite compounds

  12. TEE BARIUM CONTENT IN THE CALCAREOUS SKELETAL MATERTALS OF SOME RECENT AND

    E-print Network

    Qiu, Bo

    TEE BARIUM CONTENT IN THE CALCAREOUS SKELETAL MATERTALS OF SOME RECENT AND FOSSIL CORALS known mlxtures of the 'vrlo m inerals. Ion-exchange methods hrere utllized to separate barium from on ln the Ilvlng eorals varled from 5- 2 + IOS ppn, to L2.5 + 6.1+% ppr. ThtB varJ-atlon ln barium

  13. PHILOSOPHICAL MAGAZINE, 2003, VOL. 83, NO. 2, 165178 Synthesis and characterization of mixed-valence barium

    E-print Network

    Wang, Xiqu

    -valence barium titanates Thomas Ho« chey, Paula Olhe, Ralf Keding, Christian Ru« sselz Otto October 2001 and accepted in revised form 9 August 2002] Abstract A single-crystal barium oxotitanate and bonding in related compounds. } 1. Introduction Barium titanate (BaTiO3) is an important electroceramic

  14. 21 CFR 201.304 - Tannic acid and barium enema preparations.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 4 2013-04-01 2013-04-01 false Tannic acid and barium enema preparations. 201.304... Tannic acid and barium enema preparations. (a) It has become a widespread practice for tannic acid to be added to barium enemas to improve X-ray pictures. Tannic acid is capable of causing diminished...

  15. 21 CFR 201.304 - Tannic acid and barium enema preparations.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 4 2011-04-01 2011-04-01 false Tannic acid and barium enema preparations. 201.304... Tannic acid and barium enema preparations. (a) It has become a widespread practice for tannic acid to be added to barium enemas to improve X-ray pictures. Tannic acid is capable of causing diminished...

  16. 49 CFR 173.182 - Barium azide-50 percent or more water wet.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 49 Transportation 2 2011-10-01 2011-10-01 false Barium azide-50 percent or more water wet. 173.182 Section 173.182 Transportation Other Regulations Relating to Transportation PIPELINE AND HAZARDOUS... Class 1 and Class 7 § 173.182 Barium azide—50 percent or more water wet. Barium azide—50 percent or...

  17. MNRAS 428, 32523261 (2013) doi:10.1093/mnras/sts270 Barium abundances in Cepheids

    E-print Network

    Maciel, Walter Junqueira

    2013-01-01

    MNRAS 428, 3252­3261 (2013) doi:10.1093/mnras/sts270 Barium abundances in Cepheids S. M. Andrievsky; in original form 2012 August 28 ABSTRACT We derived the barium atmospheric abundances for a large sample to 15 kpc, so it is appropriate to investigate the existence of radial barium abundance gradients

  18. Synthesis and Structural Diversity of Barium (N,N-Dimethylamino)diboranates

    E-print Network

    Girolami, Gregory S.

    Synthesis and Structural Diversity of Barium (N,N-Dimethylamino)diboranates Scott R. Daly, Brian J. The reaction of 1 or 1 with Lewis bases that bind more strongly to barium than diethyl ether results that several of the barium complexes are monomeric in the solid state, none is appreciably volatile up to 200

  19. A comparison between excess barium and barite as indicators of carbon export

    E-print Network

    Paytan, Adina

    A comparison between excess barium and barite as indicators of carbon export Meagan Eagle and Adina in many paleoproductivity studies. Barite, the main carrier of particulate barium in the water column in some locations. We demonstrate that Baexcess (total barium minus the fraction associated

  20. PHYSICAL REVIEW A 81, 052328 (2010) Hyperfine and optical barium ion qubits

    E-print Network

    Blinov, Boris

    2010-01-01

    PHYSICAL REVIEW A 81, 052328 (2010) Hyperfine and optical barium ion qubits M. R. Dietrich,* N these profoundly quantum systems. Despite a long history in ion trapping [3­5], barium has never previously been a natural source without isotope-selective ionization [6,7]. Barium possesses a long-lived metastable state

  1. 21 CFR 201.304 - Tannic acid and barium enema preparations.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 4 2010-04-01 2010-04-01 false Tannic acid and barium enema preparations. 201.304... Tannic acid and barium enema preparations. (a) It has become a widespread practice for tannic acid to be added to barium enemas to improve X-ray pictures. Tannic acid is capable of causing diminished...

  2. Enhanced Sintering of Yttrium-Doped Barium Zirconate by Addition of ZnO

    E-print Network

    Haile, Sossina M.

    Enhanced Sintering of Yttrium-Doped Barium Zirconate by Addition of ZnO Peter Babilo and Sossina M properties of doped barium zirconate have been examined. With the use of zinc ox- ide as a sintering aid, Ba of the material under flowing CO2 showed ZnO-modified barium zirconate to exhibit excellent chemical stability

  3. 49 CFR 173.182 - Barium azide-50 percent or more water wet.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 49 Transportation 2 2014-10-01 2014-10-01 false Barium azide-50 percent or more water wet. 173.182 Section 173.182 Transportation Other Regulations Relating to Transportation PIPELINE AND HAZARDOUS... Class 1 and Class 7 § 173.182 Barium azide—50 percent or more water wet. Barium azide—50 percent or...

  4. 21 CFR 201.304 - Tannic acid and barium enema preparations.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 4 2014-04-01 2014-04-01 false Tannic acid and barium enema preparations. 201.304... Tannic acid and barium enema preparations. (a) It has become a widespread practice for tannic acid to be added to barium enemas to improve X-ray pictures. Tannic acid is capable of causing diminished...

  5. Influence of Ba content on grain size and dynamics of crystallization in barium ferrite thin films

    E-print Network

    Laughlin, David E.

    Influence of Ba content on grain size and dynamics of crystallization in barium ferrite thin films of the crystallization process, which ultimately determines the grain size, were studied in barium ferrite thin films. Rapid thermal annealing was used to crystallize the amorphous as-deposited barium ferrite films

  6. PHYSICAL REVIEW A 88, 023403 (2013) Production of translationally cold barium monohalide ions

    E-print Network

    Chapman, Michael

    2013-01-01

    PHYSICAL REVIEW A 88, 023403 (2013) Production of translationally cold barium monohalide ions M. V) We have produced sympathetically cooled barium monohalide ions BaX+ (X = F, Cl, Br) by reacting with these predictions. Producing BaX+ ions in this way is simple and allows for the study of different barium monohalide

  7. Barium Titanate Nanoparticles in Block Copolymer Tu Lee,*,, Nan Yao, Hiroaki Imai,, and Ilhan A. Aksay,

    E-print Network

    Aksay, Ilhan A.

    Barium Titanate Nanoparticles in Block Copolymer Tu Lee,*,, Nan Yao, Hiroaki Imai,, and Ilhan A-polybutadiene-polystyrene (Kraton D1102). The barium titanated Kraton thin film had remnants of the cylindrical morphology of a plain Kraton thin film with an interdomain spacing of 23 nm. The procedure of barium titanation

  8. Single-crystal barium titanate thin films by ion slicing T. Izuhara,a)

    E-print Network

    Reeves, Mark E.

    Single-crystal barium titanate thin films by ion slicing T. Izuhara,a) I.-L. Gheorma, and R. M, D.C. 20052 Received 19 September 2002; accepted 3 December 2002 Thin barium titanate films, 0.5­8 m.1063/1.1540727 Barium titanate, BaTiO3 BTO , is a ferroelectric crystal whose outstanding electrical and optical

  9. 40 CFR 721.10010 - Barium manganese oxide (BaMnO3).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Barium manganese oxide (BaMnO3). 721... Substances § 721.10010 Barium manganese oxide (BaMnO3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as barium manganese oxide (BaMnO3) (PMN...

  10. Barium ferrite thin film media with perpendicular c-axis orientation and small grain size

    E-print Network

    Laughlin, David E.

    Barium ferrite thin film media with perpendicular c-axis orientation and small grain size Zailong, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213 Barium ferrite thin films with perpendicular c conditions. The c-axis orientation of barium ferrite thin films is most sensitive to the oxygen partial

  11. 49 CFR 173.182 - Barium azide-50 percent or more water wet.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 49 Transportation 2 2012-10-01 2012-10-01 false Barium azide-50 percent or more water wet. 173.182 Section 173.182 Transportation Other Regulations Relating to Transportation PIPELINE AND HAZARDOUS... Class 1 and Class 7 § 173.182 Barium azide—50 percent or more water wet. Barium azide—50 percent or...

  12. 21 CFR 201.304 - Tannic acid and barium enema preparations.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 4 2012-04-01 2012-04-01 false Tannic acid and barium enema preparations. 201.304... Tannic acid and barium enema preparations. (a) It has become a widespread practice for tannic acid to be added to barium enemas to improve X-ray pictures. Tannic acid is capable of causing diminished...

  13. Strain effect on coercive field of epitaxial barium titanate thin films S. Choudhury,1,a

    E-print Network

    Chen, Long-Qing

    Strain effect on coercive field of epitaxial barium titanate thin films S. Choudhury,1,a Y. L. Li,1 polarizations of 001 -oriented epitaxial barium titanate thin films using the phase-field approach by strain. We use 001 -oriented epitaxial barium titanate BTO thin films as a model system. In the phase

  14. M-type barium hexaferrite synthesis and characterization for phase shifter applications

    E-print Network

    Laughlin, David E.

    M-type barium hexaferrite synthesis and characterization for phase shifter applications A. T. Wise subject to AIP license or copyright; see http://jap.aip.org/about/rights_and_permissions #12;M-type barium-type barium hexaferrite films have been grown by liquid phase epitaxy and examined by x-ray diffraction

  15. 40 CFR 721.10010 - Barium manganese oxide (BaMnO3).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Barium manganese oxide (BaMnO3). 721... Substances § 721.10010 Barium manganese oxide (BaMnO3). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as barium manganese oxide (BaMnO3) (PMN...

  16. 40 CFR 721.10010 - Barium manganese oxide (BaMnO3).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 2011-07-01 false Barium manganese oxide (BaMnO3). 721.10010...Chemical Substances § 721.10010 Barium manganese oxide (BaMnO3). (a...The chemical substance identified as barium manganese oxide (BaMnO3 )...

  17. 40 CFR 721.10010 - Barium manganese oxide (BaMnO3).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...2010-07-01 2010-07-01 false Barium manganese oxide (BaMnO3). 721.10010...Chemical Substances § 721.10010 Barium manganese oxide (BaMnO3). (a...The chemical substance identified as barium manganese oxide (BaMnO3 )...

  18. 40 CFR 721.10010 - Barium manganese oxide (BaMnO3).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...2013-07-01 2013-07-01 false Barium manganese oxide (BaMnO3). 721.10010...Chemical Substances § 721.10010 Barium manganese oxide (BaMnO3 ). (a...The chemical substance identified as barium manganese oxide (BaMnO3 )...

  19. 40 CFR 721.10010 - Barium manganese oxide (BaMnO3).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...2014-07-01 2014-07-01 false Barium manganese oxide (BaMnO3). 721.10010...Chemical Substances § 721.10010 Barium manganese oxide (BaMnO3 ). (a...The chemical substance identified as barium manganese oxide (BaMnO3 )...

  20. 40 CFR 721.10010 - Barium manganese oxide (BaMnO3).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...2012-07-01 2012-07-01 false Barium manganese oxide (BaMnO3). 721.10010...Chemical Substances § 721.10010 Barium manganese oxide (BaMnO3 ). (a...The chemical substance identified as barium manganese oxide (BaMnO3 )...

  1. 21 CFR 201.304 - Tannic acid and barium enema preparations.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...2013-04-01 2013-04-01 false Tannic acid and barium enema preparations. 201...Specific Drug Products § 201.304 Tannic acid and barium enema preparations. (a) It has become a widespread practice for tannic acid to be added to barium enemas to...

  2. 21 CFR 201.304 - Tannic acid and barium enema preparations.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...2011-04-01 2011-04-01 false Tannic acid and barium enema preparations. 201...Specific Drug Products § 201.304 Tannic acid and barium enema preparations. (a) It has become a widespread practice for tannic acid to be added to barium enemas to...

  3. 21 CFR 201.304 - Tannic acid and barium enema preparations.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...2012-04-01 2012-04-01 false Tannic acid and barium enema preparations. 201...Specific Drug Products § 201.304 Tannic acid and barium enema preparations. (a) It has become a widespread practice for tannic acid to be added to barium enemas to...

  4. 21 CFR 201.304 - Tannic acid and barium enema preparations.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...2014-04-01 2014-04-01 false Tannic acid and barium enema preparations. 201...Specific Drug Products § 201.304 Tannic acid and barium enema preparations. (a) It has become a widespread practice for tannic acid to be added to barium enemas to...

  5. 21 CFR 201.304 - Tannic acid and barium enema preparations.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...2010-04-01 2010-04-01 false Tannic acid and barium enema preparations. 201...Specific Drug Products § 201.304 Tannic acid and barium enema preparations. (a) It has become a widespread practice for tannic acid to be added to barium enemas to...

  6. Journal of Crystal Growth 271 (2004) 128133 Growth of strontium barium niobate

    E-print Network

    Osnabrück, Universität

    2004-01-01

    Journal of Crystal Growth 271 (2004) 128­133 Growth of strontium barium niobate: the liquidus. Roth Available online 11 September 2004 Abstract The liquidus­solidus phase diagram of strontium barium, and dielectric properties, strontium barium niobate, SrxBa1ÀxNb2O6--hen- ceforth denoted as SBN, is one

  7. Dielectric tunability of graded barium strontium titanate multilayers: Effect of thermal strains

    E-print Network

    Alpay, S. Pamir

    Dielectric tunability of graded barium strontium titanate multilayers: Effect of thermal strains M TEC of a multilayered barium strontium titanate Ba1-ySryTiO3 BST ferroelectric heterostructure such as barium strontium titanate Ba1-ySryTiO3 BST have emerged as leading candidates for such applications due

  8. Phase diagrams and dielectric response of epitaxial barium strontium titanate films: A theoretical analysis

    E-print Network

    Alpay, S. Pamir

    Phase diagrams and dielectric response of epitaxial barium strontium titanate films: A theoretical for publication 7 March 2002 We develop phase diagrams for single-domain epitaxial barium strontium titanate films. DOI: 10.1063/1.1473675 I. INTRODUCTION Thin films of barium strontium titanate BaxSr1 xTiO3 ,(BST

  9. Optimization of the tunability of barium strontium titanate films via epitaxial stresses

    E-print Network

    Alpay, S. Pamir

    Optimization of the tunability of barium strontium titanate films via epitaxial stresses Z.-G. Ban The tunability of epitaxial barium strontium titanate films is analyzed theoretically using a phenomenological.1063/1.1524310 I. INTRODUCTION Thin films of barium strontium titanate (BaxSr1 xTiO3, BST have long been recognized

  10. Introduction Strontium Barium Niobate k-Space Spectroscopy Results Conclusions Unraveling Relaxor Phase Transitions by

    E-print Network

    Osnabrück, Universität

    Introduction Strontium Barium Niobate k-Space Spectroscopy Results Conclusions Unraveling Relaxor 2009 WILLIAMSBURG WORKSHOP ON FUNDAMENTAL PHYSICS OF FERROELECTRICS #12;Introduction Strontium Barium ferroelectrics Introduction Strontium Barium Niobate k-Space Spectroscopy Results Conclusions SBN ­ SrxBa1-xNb2O6

  11. Optimization of High Tunability Barium Strontium Titanate Thin Films Grown by RF Magnetron

    E-print Network

    York, Robert A.

    Optimization of High Tunability Barium Strontium Titanate Thin Films Grown by RF Magnetron Abstract-- Barium strontium titanate is a solid solution perovskite with a field-dependent permittivity.7 MV/cm. I. INTRODUCTION In recent years there has been much interest in thin-film barium strontium

  12. High tunability barium strontium titanate thin films for rf circuit applications

    E-print Network

    York, Robert A.

    High tunability barium strontium titanate thin films for rf circuit applications N. K. Pervez,a) P) Large variations in the permittivity of rf magnetron sputtered thin-film barium strontium titanate have/cm. © 2004 American Institute of Physics. [DOI: 10.1063/1.1818724] Barium strontium titanate (BST) is a solid

  13. Noncollinear Optical Frequency Doubling in Strontium Barium Niobate Arthur R. Tunyagi, Michael Ulex, and Klaus Betzler*

    E-print Network

    Osnabrück, Universität

    Noncollinear Optical Frequency Doubling in Strontium Barium Niobate Arthur R. Tunyagi, Michael Ulex of a novel noncollinear optical second-harmonic generation mechanism is reported. In strontium barium niobate mechanism which we detected in crystals of strontium barium niobate (SBN)--cone-shaped second

  14. The effect of stress on the dielectric properties of barium strontium titanate thin films

    E-print Network

    Suo, Zhigang

    The effect of stress on the dielectric properties of barium strontium titanate thin films T. M Barium strontium titanate thin films are being developed as capacitors in dynamic random access memories to their large permittivities, barium strontium titan- ate BST bulk ceramics have long been used to make high

  15. Spectroscopy of Eu3+ ions in congruent strontium barium niobate crystals

    E-print Network

    Osnabrück, Universität

    Spectroscopy of Eu3+ ions in congruent strontium barium niobate crystals Ä. Andresen, A.-N. Bahar properties of single crystals of strontium barium niobate, grown from the congruently melting composition, electro-optic, pho- torefractive, and dielectric properties, the solid solution strontium barium niobate

  16. Discrete Barium Strontium Titanate (BST) Thin-Film Interdigital Varactors on Alumina: Design, Fabrication, Characterization, and

    E-print Network

    Discrete Barium Strontium Titanate (BST) Thin-Film Interdigital Varactors on Alumina: Design, Raleigh, NC-27695-7914, USA. Email:jayeshnath@ieee.org Abstract -- Discrete Barium Strontium Titanate (BST, capacitors, BST, ferroelectric, thin-film, barium strontium titanate, bandpass filter, IP3, ACPR, temperature

  17. Physico-chemical and in vitro biological study of zinc-doped calcium sulfate bone substitute.

    PubMed

    Hesaraki, Saeed; Nemati, Roghayeh; Nazarian, Hamid

    2009-10-01

    In the present study, series of Zn incorporated calcium sulfate bone cements, with different amounts of doped Zn(0, 0.74, 1.97, 3.05, 4.21 wt %) were prepared by mixing a calcium sulfate hemihydrate powder and solutions of zinc sulfate, and the effect of zinc-doping on some physical, physico-chemical, and biological properties of the cements were investigated. Pure calcium sulfate cement was also made as control, with the mentioned powder and distilled water as liquid phase. The initial setting time and compressive strength of the cement significantly changed from 17 min and 3.2 MPa for the pure calcium sulfate to 6 min and 6 MPa for the Zn-added calcium sulfate, respectively. Compared to pure calcium sulfate, more gypsum precipitates were formed in the zinc sulfate added samples with a morphology of thin, elongated, and rod-shaped crystals. The biological properties of the samples were analyzed in the terms of cell viability and cell activity on human osteosarcoma (G-292) using MTT assay and alkaline phosphatase (ALP) activity in the cell culture medium. The best increased cell density and ALP activity were achieved for the calcium sulfate cement with a content of 0.74 wt % Zn, whereas a toxic behavior was observed for the samples with Zn concentrations more than 1.97%. PMID:19358260

  18. Fluids and Sulfate Vein Formation in Gale Crater, Mars.

    NASA Astrophysics Data System (ADS)

    Schwenzer, S. P.; Bridges, J.; Leveille, R. J.; Westall, F.; Wiens, R. C.; Mangold, N.; McAdam, A.; Conrad, P. G.; Martín-Torres, J.; Zorzano, M. P.

    2014-12-01

    Curiosity detected sulfate veins crosscutting mudstones in the Sheepbed member of Gale Crater (Grotzinger et al., DOI: 10.1126/science.1242777; Manchon et al., DOI:10.1002/2013JE004588). We have used this information to evaluate the clay formation conditions in detail through thermochemical modeling (Bridges et al. submitted to JGR; this conference, session 2128) and compare the calculated fluid to those modeled for the nakhlite alteration mineralogy (Hicks et al. DOI: 10.1016/j.gca.2014.04.010, Bridges and Schwenzer, DOI: 10.1016/j.epsl.2012.09.044) and other Martian fluids. Concentrating the modeled Gale fluid though evaporation (or freezing) leads to a complex set of precipitates, which include silica, sulfate and halite. For example, 1 kg of brine produced by the alteration of a mixture of 70 % amorphous component, 20 % olivine and 10 % host rock (W/R 1000, T= 10 °C) evaporated to dryness (less that 1 % water left) will precipitate 70 mg of anhydrite, 46 mg of silica, 6.5 mg of halite and traces of pyrite, sulfur, calcite, and apatite. A fluid from this host rock with more mature alteration (W/R 100, T = 10 °C) precipitates the same minerals, but in very different abundances: the most abundant phase at dryness is halite (330 mg), followed by silica (88 mg) and anhydrite (30 mg). The calculated pH varies between 8 and 7.3 in both cases. If the evaporating brine is allowed to interact with the precipitate, a 'dirty' sulfate layer or vein filling would result, which could subsequently be refined through dissolution and re-precipitation, a mechanism that, for example, is proposed for the gypsum veins at the UK Triassic coast near Watchet (Philipp doi:10.1017/S0016756808005451). Factors that influence the nature of the precipitate include alteration stage of the host rock during clay formation, and pH and degree of fractionation of the early formed minerals from the evaporating fluid. Using REMS data we also consider desiccation of sulfates in the near surface.

  19. Characterization and distribution of undersulfated chondroitin sulfate and chondroitin in leptocephalous larvae of elopomorph fishes.

    PubMed

    Pfeiler, E

    1993-08-01

    Undersulfated chondroitin sulfate (i.e., chondroitin sulfate with sulfate: hexosamine molar ratios ranging from 0.06-0.17) has been identified as a principal glycosaminoglycan (GAG) in whole-body extracts of leptocephalous larvae of four species of marine teleost fishes, representing two orders and three families. These include the eels (Anguilliformes)Ariosoma balearicum (Congridae),Rhechias dubia (Congridae) and Ophichthus sp. (Ophichthidae) and the ladyfish (Elopiformes: Elopidae: Elops saurus). A second GAG found in relatively large amounts in A. balearicum has been identified as chondroitin. Chondroitin and undersulfated chondroitin sulfate formed distinctive precipitates during extraction and were easily separated. Undersulfated chondroitin sulfate also was extracted and purified from early metamorphosing bonefish (Albuliformes: Albulidae: Albula sp.) leptocephali, where it is a minor GAG component, and was shown to be similar in composition to the compounds obtained from eels and ladyfish. PMID:24202693

  20. Activated sludge as substrate for sulfate-reducing bacteria in acid mine drainage treatment

    SciTech Connect

    Al-Ani, W.A.G.; Henry, J.G.; Prasad, D.

    1996-11-01

    Acid mine drainage (AMD), characterized by high concentrations of sulfates and heavy metals and low pH, presents a potential hazard to the environment.Several treatment processes (chemical precipitation, ion exchange, reverse osmosis, electrodialysis and electrolytic recovery) are available, but these are often too expensive. Biological treatment of AMD, mediated by sulfate-reducing bacteria (SRB), seems promising. The objective of this study was to use activated sludge as a carbon source for the SRB and determine the most effective COD/sulfate ratio and hydraulic retention time (HRT) for reducing sulfate. Such information would be useful for the application of the proposed two-stage system to AMD treatment. Since the aim of this study was to obtain sulfate reduction and to avoid methane production, it was decided to operate the digesters initially at low COD/SO{sub 4}{sup 2{minus}} ratios of 1.0, 1.5, and 2.0.

  1. Barium-borate-flyash glasses: As radiation shielding materials

    NASA Astrophysics Data System (ADS)

    Singh, Sukhpal; Kumar, Ashok; Singh, Devinder; Thind, Kulwant Singh; Mudahar, Gurmel S.

    2008-01-01

    The attenuation coefficients of barium-borate-flyash glasses have been measured for ?-ray photon energies of 356, 662, 1173 and 1332 keV using narrow beam transmission geometry. The photon beam was highly collimated and overall scatter acceptance angle was less than 3°. Our results have an uncertainty of less than 3%. These coefficients were then used to obtain the values of mean free path (mfp), effective atomic number and electron density. Good agreements have been observed between experimental and theoretical values of these parameters. From the studies of the obtained results it is reported here that from the shielding point of view the barium-borate-flyash glasses are better shields to ?-radiations in comparison to the standard radiation shielding concretes and also to the ordinary barium-borate glasses.

  2. Chemical compositions of four barium stars

    E-print Network

    Y. C. Liang; G. Zhao; Y. Q. Chen; H. M. Qiu; B. Zhang

    2003-12-15

    Chemical compositions of four barium stars HD 26886, HD 27271, HD 50082 and HD 98839 are studied based on high resolution, high signal-to-noise Echelle spectra. Results show that all of them are disk stars. Their \\alpha and iron peak elements are similar to the solar abundances. The neutron-capture process elements are overabundant relative to the Solar. The heavy-element abundances of the strong Ba star HD 50082 are higher than those of other three mild Ba stars. Its mass is 1.32Msun (+0.28,-0.22Msun), and is consistent with the average mass of strong Ba stars (1.5Msun). For mild Ba star HD 27271 and HD 26886, the derived masses are 1.90Msun (+0.25,-0.20Msun) and 2.78Msun (+0.75,-0.78M_sun), respectively, which are consistent with the average mass of mild Ba stars. We also calculate the theoretical abundances of Ba stars by combining the AGB stars nucleosynthesis and wind accretion formation scenario of Ba binary systems. The comparisons between the observed abundance patterns of the sample stars with the theoretical results show that wind accretion scenario can explain the abundance patterns of HD 50082 and HD 27271 well, but fail to explain the abundances of HD 26886. It means that the mild Ba star HD 26886, with shorter orbital period (P11000 d), may be either a star with the heavy elements enriched by itself or a "true Ba" star.

  3. Catabolism of chondroitin sulfate.

    PubMed

    Yamada, Shuhei

    2015-06-01

    Chondroitin sulfate (CS) is a ubiquitous component of the cell surface and extracellular matrix of animal tissues. CS chains are covalently bound to a core protein to form a proteoglycan, which is involved in various biological events including cell proliferation, migration, and invasion. Their functions are executed by regulating the activity of bioactive proteins, such as growth factors, morphogens, and cytokines. This review article focuses on the catabolism of CS. This catabolism predominantly occurs in lysosomes to control the activity of CS-proteoglycans. CS chains are fragmented by endo-type glycosidase(s), and the resulting oligosaccharides are then cleaved into monosaccharide moieties from the nonreducing end by exoglycosidases and sulfatases. However, the endo-type glycosidase responsible for the systemic catabolism of CS has not yet been identified. Based on recent advances in studies on hyaluronidases, which were previously considered to be hyaluronan-degrading enzymes, it appears that they recognize CS as their original substrate rather than hyaluronan and acquired hyaluronan-hydrolyzing activity at a relatively late stage of evolution. PMID:26204402

  4. Ionization and expansion of barium clouds in the ionosphere

    NASA Technical Reports Server (NTRS)

    Ma, T.-Z.; Schunk, R. W.

    1993-01-01

    A recently envelope 3D model is used here to study the motion of the barium clouds released in the ionosphere, including the ionization stage. The ionization and the expansion of the barium clouds and the interaction between the clouds and the background ions are investigated using three simulations: a cloud without a directional velocity, a cloud with an initial velocity of 5 km/s across the B field, and a cloud with initial velocity components of 2 km/s both along and across the B field.

  5. Photoionization and Photoelectric Loading of Barium Ion Traps

    E-print Network

    A. V. Steele; L. R. Churchill; P. F. Griffin; M. S. Chapman

    2007-03-22

    Simple and effective techniques for loading barium ions into linear Paul traps are demonstrated. Two-step photoionization of neutral barium is achieved using a weak intercombination line (6s2 1S0 6s6p 3P1, 791 nm) followed by excitation above the ionization threshold using a nitrogen gas laser (337 nm). Isotopic selectivity is achieved by using a near Doppler-free geometry for excitation of the triplet 6s6p 3P1 state. Additionally, we report a particularly simple and efficient trap loading technique that employs an in-expensive UV epoxy curing lamp to generate photoelectrons.

  6. Study of the photovoltaic effect in thin film barium titanate

    NASA Technical Reports Server (NTRS)

    Grannemann, W. W.; Dharmadhikari, V. S.

    1981-01-01

    The photoelectric effect in structures consisting of metal deposited barium titanate film silicon is described. A radio frequency sputtering technique is used to deposit ferroelectric barium titantate films on silicon and quartz. Film properties are measured and correlated with the photoelectric effect characteristics of the films. It was found that to obtain good quality pin hole free films, it is necessary to reduce the substrate temperature during the last part of the deposition. The switching ability of the device with internal applied voltage is improved when applied with a ferroelectric memory device.

  7. Ferroelastic domains in lead-free barium zirconate titanate - barium calcium titanate piezoceramics

    NASA Astrophysics Data System (ADS)

    Ehmke, Matthias Claudius

    Piezoelectricity was first discovered by Pierre and Jaque Curie in the year 1880. Nowadays, piezoelectric materials are used in many application such as high voltage generation in gas igniters, actuation in micro-positioning devices, generation and detection of acoustic waves, emitters and receivers for sonar technology, ultrasonic cleaning, ultrasound medical therapy, and micropumps for ink-jet printers. The most commonly used piezoelectric material since the 1950's is the solid solution system lead zirconate titanate (PZT) that offers high piezoelectric performance under a large range of operating conditions. However, the toxicity of lead requires the replacement of PZT. The studied lead-free alternatives are commonly based on potassium sodium niobate (KNN) and bismuth sodium titanate (BNT), and more recently zirconium and calcium substituted barium titanate (BZT-BCT). The BZT-BCT system exhibits large piezoelectric coefficients that can exceed even those of most PZT compositions under certain conditions. Piezoelectricity was first discovered by Pierre and Jaque Curie in the year 1880. Nowadays, piezoelectric materials are used in many application such as high voltage generation in gas igniters, actuation in micro-positioning devices, generation and detection of acoustic waves, emitters and receivers for sonar technology, ultrasonic cleaning, ultrasound medical therapy, and micropumps for ink-jet printers. The most commonly used piezoelectric material since the 1950's is the solid solution system lead zirconate titanate (PZT) that offers high piezoelectric performance under a large range of operating conditions. However, the toxicity of lead requires the replacement of PZT. The studied lead-free alternatives are commonly based on potassium sodium niobate (KNN) and bismuth sodium titanate (BNT), and more recently zirconium and calcium substituted barium titanate (BZT-BCT). The BZT-BCT system exhibits large piezoelectric coefficients that can exceed even those of most PZT compositions under certain conditions.

  8. Sulfate decomposition by bacterial leaching

    SciTech Connect

    Deveci, N.; Delaloglu, C.G.

    1995-04-01

    Sulfate disposal is the main problem of many industrial effluents, such as excess sulfuric acid, gypsum, coal desulfurization byproducts, acid-mine waters, and general metallurgical effluents. It has been established that sulfate present in wastes can be converted to elemental sulfur by bacterial mutualism. This study presents the results of an investigation of the industrial feasibility of utilizing a biological system capable of converting hydrous calcium sulfate (gypsum) to elemental sulfur. Gypsum, which was used in this study, is a byproduct of the fertilizer industry. The biological system is referred to as a bacterial mutualism, and involves Desulfovibrio desulfuricans for sulfate conversion and Chlorobium thiosulfatophilum for hydrogen sulfide conversion. Bacterial mutualism and utilization of sulfate were investigated by means of a two-stage anaerobic system. In the first stage, a gas purge system was used for sulfate conversion to sulfide, and it was found that maximum conversion is 34%. In the second stage, a static culture system was used for sulfide conversion to sulfur with a conversion of 92%. 14 refs., 5 tabs.

  9. Laxatives as colonic preparation for barium enema: the patient's viewpoint.

    PubMed

    Coombs, B M

    1983-09-01

    The choice of method of bowel preparation before double contrast barium enema should be influenced by patients' reactions and how it affects them. In support of this view, radiographers carried out a study on the effects of a laxative. PMID:6635154

  10. [Is the barium enema preparation a good preparation for echography?].

    PubMed

    Scherrer, A; Menu, Y

    1983-01-01

    A comparative study of 50 patients without previous preparation and 50 who were prepared by a barium enema and low residue diet demonstrated that this method of preparing for ultrasonography improved visibility of the pancreas and the overall quality of the examination. However, the difference in patients with or without previous preparation was not sufficient to justify its routine use. PMID:6644661

  11. PROPOSED ORAL REFERENCE DOSE (RFD) FOR BARIUM AND COMPOUNDS

    EPA Science Inventory

    The Integrated Risk Information System (IRIS) is a database of EPA's consensus opinion of the human health effects that may result from exposure to various substances found in the environment. A Toxicological Review and IRIS Summary were prepared for barium and compounds in 1998 ...

  12. BARIUM AND RADIUM IN WATER TREATMENT PLANT WASTES

    EPA Science Inventory

    Water treatment plants at nine locations (10 plants) in Illinois and Iowa were studied to determine the characteristics and disposal practices for the sludge, brine, and backwash water containing radium (Ra) and/or barium (Ba). The treatment processes in these ten plants include ...

  13. HEALTH EFFECTS OF HUMAN EXPOSURE TO BARIUM IN DRINKING WATER

    EPA Science Inventory

    The overall objective of this study was to examine by epidemiologic and supportive laboratory studies, the human health effects associated with ingestion of barium in drinking water exceeding the U.S. drinking water standard of 1.0 mg/l. The incidence of cardiovascular mortality ...

  14. Dynamics of a barium release in the magnetospheric tail

    NASA Technical Reports Server (NTRS)

    Mende, S. B.; Swenson, G. R.; Geller, S. P.; Doolittle, J. H.; Haerendel, G.

    1989-01-01

    The late time behavior of the May 13, 1985 magnetotail barium cloud is examined. The bulk dynamics of the cloud are studied based on triangulated data and data from Fabry-Perot Doppler velocity measurements. The changes in cloud morphology in relation to the in situ measurements made by the Ion Release Module satellite are discussed.

  15. REMOVING BARIUM AND RADIUM THROUGH CALCIUM CATION EXCHANGE

    EPA Science Inventory

    The removal of barium (Ba) and radium (Ra), which are found in many groundwater sources, was achieved in laboratory studies with an ion exchange process. In the studies, a strong acid resin in the calcium form effectively removed Ba(+2) and Ra (+2) to meet standards. The resin wa...

  16. BARIUM AND RADIUM REMOVAL FROM GROUNDWATER BY ION EXCHANGE

    EPA Science Inventory

    The primary objective of this study was to determine the applicability of weak acid exchange resin in the hydrogen form for removal of hardness, barium and radium from groundwater. Weak acid resin in the hydrogen form eliminates the addition of sodium to drinking water. The capac...

  17. Modeling microbially induced calcite precipitation

    E-print Network

    Cirpka, Olaf Arie

    Modeling microbially induced calcite precipitation Erlangen, November 27th 2014 Johannes Hommel Induced Calcite Precipitation (MICP) is investigated as sealing technology. It is used as an exemplary / detachment · Urea hydrolysis · Precipitation / dissolution of calcite · Clogging calcite precipitate CO2

  18. The biogeography of export productivity across the Cretaceous-Paleogene boundary as inferred from sediment mixing and biogenic barium

    NASA Astrophysics Data System (ADS)

    Hull, P. M.; Norris, R. D.; Franks, P. J.

    2009-12-01

    The impact at the Cretaceous-Paleogene (KPg) boundary is thought to have precipitated a sudden decrease in global export productivity, in addition to widespread extinction. A global decrease in oceanic export productivity gains support from the collapse in ?13C gradients between surface-dwelling and deep-ocean foraminifera and decreased sedimentation rates. However, a growing body of evidence suggests a milder, spatially heterogeneous perturbation. Here we investigate the magnitude and spatial distribution of export production across the KPg boundary using two proxies, the depth of sediment mixing and the accumulation of biogenic barium. In the modern ocean, the depth of sediment mixing is correlated to the amount of organic matter reaching the sea floor as a function of water depth and export production. We calculate the relative depth of sediment mixing by fitting mixing models to the shape of iridium anomalies. In all 10 sites examined globally, export productivity is indicated by the presence of sediment mixing. The depth of mixing inferred from a subset of these sites records an inter-site range in mixing depths greater than the range measured in the modern ocean. Biogenic barium (measured by Ba/Al ratios) indicates a spatially heterogeneous effect of boundary events on export production as well. While biogenic barium decreases at most sites studied, the magnitude of this decline varies among sites, with one site in the North Pacific failing to record a sustained depression. Together, our results suggest that the decrease in export productivity following the KPg boundary event may have been a regional, albeit widespread, phenomenon.

  19. Preliminary study of the CRRES magnetospheric barium releases

    NASA Technical Reports Server (NTRS)

    Huba, J. D.; Bernhardt, P. A.; Lyon, J. G.

    1992-01-01

    Preliminary theoretical and computational analyses of the Combined Release and Radiation Effects Satellite (CRRES) magnetospheric barium releases are presented. The focus of the studies is on the evolution of the diamagnetic cavity which is formed by the barium ions as they expand outward, and on the structuring of the density and magnetic field during the expansion phase of the releases. Two sets of simulation studies are discussed. The first set is based upon a 2D ideal MHD code and provides estimates of the time and length scales associated with the formation and collapse of the diamagnetic cavity. The second set uses a nonideal MHD code; specifically, the Hall term is included. This additional term is critical to the dynamics of sub-Alfvenic plasma expansions, such as the CRRES barium releases, because it leads to instability of the expanding plasma. Detailed simulations of the G4 and G10 releases were performed. In both cases the expanding plasma rapidly structured: the G4 release structured at time t less than about 3 s and developed scale sizes of about 1-2 km, while the G10 release structured at time t less than about 22 s and developed scale sizes of about 10-15 km. It is also found that the diamagnetic cavity size is reduced from those obtained from the ideal MHD results because of the structure. On the other hand, the structuring allows the formation of plasma blobs which appear to free stream across the magnetic field; thus, the barium plasma can propagate to larger distances traverse to the magnetic field than the case where no structuring occurs. Finally, a new normal mode of the system was discovered which may be excited at the leading edge of the expanding barium plasma.

  20. Studies on effective utilization of precipitates from neutralized mine drainage

    SciTech Connect

    Harada, Taneomi

    1995-12-31

    Mine drainage has high acidity and sometimes contains more than the allowable concentration of ionized iron. In such a case, mine drainage is neutralized with calcium carbonate and calcium hydroxide to separate precipitates, such as the iron hydroxide and gypsum generated. Currently, most of these precipitates are not utilized and are accumulated in tailing dams. As a result, the service life of the tailing dams is reduced. This becomes a matter of concern, since securing sites for such dams is difficult. A most effective means of solving this problem would be to promote utilization of these neutralized precipitates. This paper reports on the results of studies on neutralized precipitates produced at the old Matsuo Mine (Iwate Prefecture), which has the largest neutralization treatment facility in Japan. As a result of the studies, the following was proposed regarding application of neutralized precipitates. Utilization as ferrite: mix ferrous hydroxide and ferric hydroxide in water to synthesize magnetite-like ferrite, to be used in the manufacture of magnetic markers for a mobility support system for blind pedestrians, or in producing magnetic fluids for sink-and-float separation of nonmagnetic metals and nonmetals. Utilization as hematite: bake ferric hydroxide to produce hematite, thereby extracting metallic iron for paint pigment as well as for the manufacture of ironware by local industry. Production of aluminum sulfate: precipitate aluminum ions from water and add sulfuric acid to produce aluminum sulfate.

  1. LONG-RANGE TRANSPORT AND TRANSFORMATION OF SO2 AND SULFATE

    EPA Science Inventory

    Technical descriptions and computer programs are presented for two models that calculate long-range transport, diffusion, transformation of SO2 to sulfate, and dry and precipitation deposition of initially emitted SO2. One model treats the mixing layer height as constant; the oth...

  2. Time trends in Canadian air and precipitation chemistry data

    SciTech Connect

    Ro, C.U.; Sirois, A.; Vet, R.J.

    1997-12-31

    Wet deposition measurements from various monitoring networks in Canada and the US were combined and integrated to estimate the total mass of non-sea-salt sulfate, nitrate, H{sup +} and cations (Ca{sup ++} + Mg{sup ++} + K{sup +}) wet deposited annually to eastern North America. The results showed that the integrated wet deposition of sulfate and cations (Ca{sup ++} + Mg{sup ++} + K{sup +}) decreased markedly from the early 1980s to the early 1990s while the integrated nitrate and H{sup +} deposition did not. It therefore appears that the decrease in the integrated cation deposition offset the decrease in sulfate, resulting in little change to the integrated deposition of free acidity. The same conclusion was obtained from a long-term trends analysis of precipitation chemistry data from 16 sites across eastern Canada. A geometric trends model was fitted to daily ion concentrations in precipitation. The long-term trends indicate that sulfate concentrations in precipitation decreased significantly from the early 1980s to the early 1990s at 12 of the 16 sites, mostly between the early 1980s and the mid-to-late 1980s. Concurrent with these decreases were declining base cation concentrations at 12 of the 16 sites and constant or increasing nitrate concentrations at 9 of the 16 sites. As a result, the concentration of hydronium ion in precipitation remained constant at 8 of the 16 sites and varied between increasing and decreasing trends at the other sites. A similar time series analysis of CAPMoN ambient air data showed that concentrations of sulphur dioxide decreased significantly from the beginning of the 1980s to the beginning of the 1990s at 5 of the 6 sites where long enough data records were available. Similar but less consistent trends were found in the case of sulfate. Vapor phase nitric acid concentrations showed increasing long-term trends over the same period.

  3. Global Precipitation Measurement

    NASA Technical Reports Server (NTRS)

    Hou, Arthur Y.; Skofronick-Jackson, Gail; Kummerow, Christian D.; Shepherd, James Marshall

    2008-01-01

    This chapter begins with a brief history and background of microwave precipitation sensors, with a discussion of the sensitivity of both passive and active instruments, to trace the evolution of satellite-based rainfall techniques from an era of inference to an era of physical measurement. Next, the highly successful Tropical Rainfall Measuring Mission will be described, followed by the goals and plans for the Global Precipitation Measurement (GPM) Mission and the status of precipitation retrieval algorithm development. The chapter concludes with a summary of the need for space-based precipitation measurement, current technological capabilities, near-term algorithm advancements and anticipated new sciences and societal benefits in the GPM era.

  4. Precipitation of relativistic electrons

    NASA Astrophysics Data System (ADS)

    Parks, G. K.; Lee, J. J.; Lee, E. S.; Sample, J.; McCarthy, M.

    2012-11-01

    Precipitation of relativistic electrons observed in Earth's auroral zone occurs on the morning and evening local hours. The morning precipitation is impulsive with durations of about 0.25s (microbursts). The evening precipitation is relatively smooth with variations on minute time scales. Mechanisms for the relativistic electron precipitation remain unknown. Microbursts with relativistic energies come from polar orbiting satellites and they have not been seen on balloon-borne detectors. Relativistic electrons on the evening hours are detected by balloonborne detectors and have not been reported by satellites. We anticipate the upcoming missions could resolve this dilemma.

  5. Uncertainties in Arctic precipitation

    NASA Astrophysics Data System (ADS)

    Majhi, Ipshita; Alexeev, Vladimir; Cherry, Jessica; Groisman, Pasha; Cohen, Judah

    2013-04-01

    Precipitation is an essential and highly variable component of the freshwater budget, and solid precipitation in particular, has a major impact on the local and global climate. The impacts of snow on the surface energy balance are tremendous, as snow has a higher albedo than any other naturally occurring surface condition. Documenting the instrumentally observed precipitation climate records presents its own challenges since the stations themselves undergo many changes in the course of their operation.Though it is crucial to accurately measure precipitation as a means to predict change in future water budgets, estimates of long-term precipitation are riddled with measurement biases. Some of the challenges facing reliable measurement of solid precipitation include missing data, gage change, discontinued stations, trace precipitation, blizzards, wetting losses when emptying the gage, and evaporation between the time of event and the time of measurement. Rain measurements likewise face uncertainties such as splashing of rain out of the gage, evaporation, and extreme events, though the magnitude of these impacts on overall measurement is less than that faced by solid precipitation. In all, biases can be so significant that they present major problems for the use of precipitation data in climate studies.

  6. Cerium oxalate precipitation

    SciTech Connect

    Chang, T.P.

    1987-02-01

    Cerium, a nonradioactive, common stand-in for plutonium in development work, has been used to simulate several plutonium precipitation processes at the Savannah River Laboratory. There are similarities between the plutonium trifluoride and the cerium oxalate precipitations in particle size and extent of plating, but not particle morphology. The equilibrium solubility, precipitation kinetics, particle size, extent of plating, and dissolution characteristics of cerium oxalate have been investigated. Interpretations of particle size and plating based on precipitation kinetics (i.e., nucleation and crystal growth) are presented. 16 refs., 7 figs., 6 tabs.

  7. A procoagulant chemically sulfated mannan.

    PubMed

    Gracher, Ana Helena P; Santana, Aline G; Cipriani, Thales R; Iacomini, Marcello

    2016-01-20

    Disorders of hemostasis can produce innumerous problems. Polysaccharides have been studied both as anticoagulant and as procoagulant agents. A mannan with a main chain of ?-(1?6)-linked-Manp units, branched at O-2 mainly by side-chains of 2-O-linked-?-Manp units was chemically sulfated, structurally characterized by NMR and GC-MS (methylation, desulfation and methylation with trideuterated iodomethane), and tested in vitro and in vivo on blood coagulation models. Chemical analyses indicate a high degree of substitution on the sulfated polysaccharide. This polymer acted as a procoagulant agent, increasing blood coagulation in normal and hemophilic plasma, activated platelet aggregation and also decreased ex vivo aPTT. Polymers such as the sulfated mannan could be a helpful source of hemostatic agents to prevent hemorrhagic states. PMID:26572344

  8. Methods of producing sulfate salts of cations from heteroatomic compounds and dialkyl sulfates and uses thereof

    SciTech Connect

    Friesen, Cody A.; Wolfe, Derek; Johnson, Paul Bryan

    2015-09-29

    Methods of preparing sulfate salts of heteroatomic compounds using dialkyl sulfates as a primary reactant are disclosed. Also disclosed are methods of making ionic liquids from the sulfate salts of the heteroatomic compound, and electrochemical cells comprising the ionic liquids.

  9. Design, testing, fabrication and launch support of a liquid chemical barium release payload (utilizing the liquid fluorine-barium salt/hydrazine system)

    NASA Technical Reports Server (NTRS)

    Stokes, C. S.; Smith, E. W.; Murphy, W. J.

    1972-01-01

    A payload was designed which included a cryogenic oxidizer tank, a fuel tank, and burner section. Release of 30 lb of chemicals was planned to occur in 2 seconds at the optimum oxidizer to fuel ratio. The chemicals consisted of 17 lb of liquid fluorine oxidizer and 13 lb of hydrazine-barium salt fuel mixture. The fuel mixture was 17% barium chloride, 16% barium nitrate, and 67% hydrazine, and contained 2.6 lb of available barium. Two significant problem areas were resolved during the program: explosive valve development and burner operation. The release payload was flight tested, from Wallops Island, Virginia. The release took place at an altitude of approximately 260 km. The release produced a luminous cloud which expanded very rapidly, disappearing to the human eye in about 20 seconds. Barium ion concentration slowly increased over a wide area of sky until measurements were discontinued at sunrise (about 30 minutes).

  10. Surface studies of barium and barium oxide on tungsten and its application to understanding the mechanism of operation of an impregnated tungsten cathode

    NASA Technical Reports Server (NTRS)

    Forman, R.

    1976-01-01

    Surface studies have been made of multilayer and monolayer films of barium and barium oxide on a tungsten substrate. The purpose of the investigation was to synthesize the surface conditions that exist on an activated impregnated tungsten cathode and obtain a better understanding of the mechanism of operation of such cathodes. The techniques employed in these measurements were Auger spectroscopy and work-function measurements. The results of this study show that the surface of an impregnated cathode is identical to that observed for a synthesized monolayer or partial monolayer of barium on oxidized tungsten by evaluating Auger spectra and work-function measurements. Data obtained from desorption studies of barium monolayers on a tungsten substrate in conjunction with Auger and work-function results have been interpreted to show that throughout most of its life an impreganated cathode has a partial monolayer, rather than a monolayer, of barium on its surface.

  11. The possible role of sulfate-reduction kinetics in the formation of hydrothermal uranium deposits

    USGS Publications Warehouse

    Spirakis, Charles S.

    1981-01-01

    Sulfate is known to be an active oxidizing agent at high temperatures; however, both experimental and geologic evidence indicate that as a hydrothermal solution cools (to about 200 degrees C, depending on pH) kinetic factors slow the rate at which sulfate enters into redox reactions. This retardation of sulfate reduction diminishes the effectiveness of sulfate as an oxidizing agent. Consequently, as cooling proceeds, the reducing effect of H2S (and other reduced species) is not balanced with the oxidizing effect of SO (super -2) 4 to the same extent as at higher temperatures. The result is a progressively more reducing solution, which is precisely what is needed to precipitate reduced uranium minerals and to generate the paragenetic sequence observed in these deposits. The same mechanism may apply to other types of epithermal deposits.

  12. Volumetric determination of uranium titanous sulfate as reductant before oxidimetric titration

    USGS Publications Warehouse

    Wahlberg, J.S.; Skinner, D.L.; Rader, L.F., Jr.

    1957-01-01

    Need for a more rapid volumetric method for the routine determination of uranium in uranium-rich materials has led to the development of a method that uses titanous sulfate as a reductant before oxidimetric titration. Separation of the hydrogen sulfide group is not necessary. Interfering elements precipitated by cupferron are removed by automatic filtrations made simultaneously rather than by the longer chloroform extraction method. Uranium is reduced from VI to IV by addition of an excess of titanous sulfate solution, cupric ion serving as an indicator by forming red metallic copper when reduction is complete. The copper is reoxidized by addition of mercuric perchlorate. The reduced uranium is then determined by addition of excess ferric sulfate and titration with ceric sulfate. The method has proved to be rapid, accurate, and economical.

  13. Background levels of air and precipitation quality for Europe

    NASA Astrophysics Data System (ADS)

    Szepesi, DezsöJ.; Fekete, Katalin E.

    This paper is intended to be used by specialists engaged in air and precipitation quality management on regional and continental scales. Major goals are to establish definition, methodology and specific values of background air and precipitation quality for sulfur (S) and nitrogen (N) species to be used in practical applications of air resources management. Major findings are the following: (a) 69% of SO 2 and 63 % of NO 2 concentration over Europe originate from continental scale anthropogenic sources, (b) 15% of precipitation sulfate and 11% of precipitation nitrate over Europe are contributed by hemispheric background, (c) hemispheric background pollution values for Europe were found as 1.25 ?g (SO 2-S)m -3, 0.80 ?g (SO 42--S)m -3, 0.157 mg ( SO42-- S) l-1 and 0.04 mg ( NO3-- N)? -1.

  14. Stability of Magnesium Sulfate Minerals in Martian Environments

    NASA Technical Reports Server (NTRS)

    Marion, G. M.; Kargel, J. S.

    2005-01-01

    Viking Lander, Pathfinder, and Mars Exploration Rover missions to Mars have found abundant sulfur in surface soils and rocks, and the best indications are that magnesium sulfates are among the key hosts. At Meridiani Planum, MgSO4 salts constitute 15 to 40 wt.% of sedimentary rocks. Additional S is hosted by gypsum and jarosite. Reflectance and thermal emission spectroscopy is consistent with the presence of kieserite (MgSO4 H2O) and epsomite (MgSO4*7H2O). Theoretically, the dodecahydrate (MgSO4*12H2O) should also have precipitated. We first examine theoretically which MgSO4 minerals should have precipitated on Mars, and then how dehydration might have altered these minerals.

  15. Global Precipitation Measurement Poster

    NASA Technical Reports Server (NTRS)

    Azarbarzin, Art

    2010-01-01

    This poster presents an overview of the Global Precipitation Measurement (GPM) constellation of satellites which are designed to measure the Earth's precipitation. It includes the schedule of launches for the various satellites in the constellation, and the coverage of the constellation, It also reviews the mission capabilities, and the mission science objectives.

  16. Barium and Yttrium abundance in intermediate-age and old open clusters

    E-print Network

    Mishenina, T; Carraro, G; Kovtyukh, V V; Yegorova, I A

    2013-01-01

    Barium is a neutron capture element, that, in open clusters, is frequently over-abundant with respect to the Iron. A clear explanation for this is still missing. Additionally, its gradient across the Galactic disk is poorly constrained. We measure the abundance of yttrium and barium using the synthetic spectrum method from UVES high-resolution spectra of eight distant open clusters, namely Ruprecht 4, Ruprecht 7, Berkeley 25, Berkeley 73, Berkeley 75, NGC 6192, NGC 6404, and NGC 6583. The barium abundance was estimated using NLTE approximation. We confirm that Barium is indeed over-abundant in most clusters, especially young clusters. Finally, we investigated the trend of yttrium and barium abundances as a function of distance in the Galaxy and ages. Several scenarios for the barium over-abundance are then discussed.

  17. Life Model of Hollow Cathodes Using a Barium Calcium Aluminate Impregnated Tungsten Emitter

    NASA Technical Reports Server (NTRS)

    Kovaleski, S. D.; Burke, Tom (Technical Monitor)

    2001-01-01

    Hollow cathodes with barium calcium aluminate impregnated tungsten emitters for thermionic emission are widely used in electric propulsion. These high current, low power cathodes are employed in ion thrusters, Hall thrusters, and on the International Space Station in plasma contactors. The requirements on hollow cathode life are growing more stringent with the increasing use of electric propulsion technology. The life limiting mechanism that determines the entitlement lifetime of a barium impregnated thermionic emission cathode is the evolution and transport of barium away from the emitter surface. A model is being developed to study the process of barium transport and loss from the emitter insert in hollow cathodes. The model accounts for the production of barium through analysis of the relevant impregnate chemistry. Transport of barium through the approximately static gas is also being treated. Finally, the effect of temperature gradients within the cathode are considered.

  18. Aerobic sulfate reduction in microbial mats

    NASA Technical Reports Server (NTRS)

    Canfield, Donald E.; Des Marais, David J.

    1991-01-01

    Measurements of bacterial sulfate reduction and dissolved oxygen (O2) in hypersaline bacterial mats from Baja California, Mexico, revealed that sulfate reduction occurred consistently within the well-oxygenated photosynthetic zone of the mats. This evidence that dissimilatory sulfate reduction can occur in the presence of O2 challenges the conventional view that sulfate reduction is a strictly anaerobic process. At constant temperature, the rates of sulfate reduction in oxygenated mats during daytime were similar to rates in anoxic mats at night: thus, during a 24-hour cycle, variations in light and O2 have little effect on rates of sulfate reduction in these mats.

  19. The biological reduction of selenate and sulfate in agricultural drainage water

    SciTech Connect

    Owens, L.P.

    1991-01-01

    In many areas of the western US, subsurface drainage is produced when restrictive soils are irrigated and drained. The agricultural drainage water is saline and in many areas the concentration of selenium exceeds 100 {mu}g/L. Sulfate is present at concentrations ranging from 1,000 mg/L to 10,000 mg/L. Two upflow anaerobic sludge blanket reactors were constructed to evaluate the fate of selenate in a biological reactor treating a synthetic agricultural drainage water under sulfate-reducing conditions. Both lactate and molasses were evaluated as carbon sources for the microbiological process. Sulfate reducing conditions were established in both reactors with a 95+% reduction in sulfate from initial levels of 3,600 mg/L SO{sub 4}{sup {minus}2} Sulfate was reduced to sulfide via the dissimilatory sulfate reduction pathway. Selenate was reduced to elemental selenium through a sulfate-independent dissimilatory reduction pathway. The elemental selenium formed seleno-polysulfides in the sulfidic environment of the reactor. Conversion to seleno-polysulfides increased the solubility of the elemental selenium. The seleno-polysulfides were precipitated with iron salts. A residual total selenium level of about 20% of the initial 350 {mu}g/L Se remained in the effluent after precipitation of the seleno-polysulfides due to the presence of soluble organic selenium compounds. Denitrification of the influent nitrate at a concentration of 214 mg/L as NO{sub 3}{sup {minus}} was complete. A treatment scheme was proposed for the simultaneous removal of selenium, nitrate, and sulfate from agricultural drainage waters.

  20. The Skylab barium plasma injection experiments. I - Convection observations

    NASA Technical Reports Server (NTRS)

    Wescott, E. M.; Stenbaek-Nielsen, H. C.; Davis, T. N.; Peek, H. M.

    1976-01-01

    Two barium-plasma injection experiments were carried out during magnetically active periods in conjunction with the Skylab 3 mission. The high-explosive shaped charges were launched near dawn on November 27 and December 4, 1973, UT. In both cases, the AE index was near 400 gammas, and extensive pulsating auroras covered the sky. The first experiment, Skylab Alpha, occurred in the waning phase of a 1000-gamma substorm, and the second, Skylab Beta, occurred in the expansive phase of an 800-gamma substorm. In both, the convection was generally magnetically eastward, with 100-km-level electric fields near 40 mV/m. However, in the Alpha experiment the observed orientation of the barium flux tube fit theoretical field lines having no parallel current, but the Beta flux-tube orientation indicated a substantial upward parallel sheet current.

  1. Observations and theory of the AMPTE magnetotail barium releases

    NASA Technical Reports Server (NTRS)

    Bernhardt, P. A.; Roussel-Dupre, R. A.; Pongratz, M. B.; Haerendel, G.; Valenzuela, A.

    1987-01-01

    The barium releases in the magnetotail during the Active Magnetospheric Particle Tracer Explorers (AMPTE) operation were monitored by ground-based imagers and by instruments on the Ion Release Module. After each release, the data show the formation of a structured diamagnetic cavity. The cavity grows until the dynamic pressure of the expanding ions balances the magnetic pressure on its surface. The magnetic field inside the cavity is zero. The barium ions collect on the surface of the cavity, producing a shell. Plasma irregularities form along magnetic field lines draped over the surface of the cavity. The scale size of the irregularities is nearly equal to the thickness of the shell. The evolution and structuring of the diamagnetic cavity are modeled using magnetohydrodynamics theory.

  2. Numerical simulation of a radially injected barium cloud

    NASA Technical Reports Server (NTRS)

    Swift, D. W.; Wescott, E. M.

    1981-01-01

    Electrostatic two-dimensional numerical simulations of a radially symmetric barium injection experiment demonstrate that ions created by solar UV irradiation are electrostatically bound to the electrons which remain tied to the field lines on which they are created. Two possible instabilities are identified, but neither of them causes the barium plasma cloud to polarize in a way that would permit the plasma to keep up with the neutrals. In a second model, the velocity of the neutrals is allowed to be a function of the azimuthal angle. Here, a portion of the cloud does polarize in a way that allows a portion of the plasma to detach and move outward at the approximate speed of the neutrals. No rapid detachment is found when only the density of the neutrals is given an azimuthal asymmetry.

  3. NASA/Max Planck Institute Barium Ion Cloud Project.

    NASA Technical Reports Server (NTRS)

    Brence, W. A.; Carr, R. E.; Gerlach, J. C.; Neuss, H.

    1973-01-01

    NASA and the Max Planck Institute for Extraterrestrial Physics (MPE), Munich, Germany, conducted a cooperative experiment involving the release and study of a barium cloud at 31,500 km altitude near the equatorial plane. The release was made near local magnetic midnight on Sept. 21, 1971. The MPE-built spacecraft contained a canister of 16 kg of Ba CuO mixture, a two-axis magnetometer, and other payload instrumentation. The objectives of the experiment were to investigate the interaction of the ionized barium cloud with the ambient medium and to deduce the properties of electric fields in the proximity of the release. An overview of the project is given to briefly summarize the organization, responsibilities, objectives, instrumentation, and operational aspects of the project.

  4. Study of the photovoltaic effect in thin film barium titanate

    NASA Technical Reports Server (NTRS)

    Grannemann, W. W.; Dharmadhikari, V. S.

    1982-01-01

    Ferroelectric films of barium titanate were synthesized on silicon and quartz substrates, and the photoelectric effect in the structure consisting of metal deposited ferroelectric barium titanate film silicon was studied. A photovoltage with polarity that depends on the direction of the remanent polarization was observed. The deposition of BaTiO3 on silicon and fused quartz substrates was accomplished by an rf sputtering technique. A series of experiments to study the growth of ferroelectric BaTiO3 films on single crystal silicon and fused quartz substrates were conducted. The ferroelectric character in these films was found on the basis of evidence from the polarization electric field hysteresis loops, capacitance voltage and capacitance temperature techniques and from X-ray diffraction studies.

  5. DYNAMICS OF AUTOMOTIVE SULFATE EMISSIONS

    EPA Science Inventory

    A preliminary assessment of the potential environmental impact of automotive sulfuric acid (or sulfate) aerosol has been made by analyzing the aerosol dynamics. This analysis leads to the prediction of ambient automotive sulfuric acid aerosol concentrations over and around a larg...

  6. Status of Copper Sulfate - 2010

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This is brief overview of the Technical Sections completed and being worked on for the New Animal Drug Application (NADA) for copper sulfate. Initial Label Claim (Ich on catfish): 1) Human Food Safety - Complete for all fin fish - February 2004. This includes human intestinal microflora issues,...

  7. Status of copper sulfate - 2008

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This is brief overview of the Technical Sections completed and being worked on for the New Animal Drug Application (NADA) for copper sulfate. Initial Label Claim (Ich on catfish): 1) Human Food Safety - Complete for all fin fish – February 2004. This includes human intestinal microflora issues,...

  8. Chiral Crystallization of Ethylenediamine Sulfate

    ERIC Educational Resources Information Center

    Koby, Lawrence; Ningappa, Jyothi B.; Dakesssian, Maria; Cuccia, Louis A.

    2005-01-01

    The optimal conditions for the crystallization of achiral ethylenediamine sulfate into large chiral crystals that are ideal for polarimetry studies and observation using Polaroid sheets are presented. This experiment is an ideal undergraduate experiment, which clearly demonstrates the chiral crystallization of an achiral molecule.

  9. Status of copper sulfate - 2007

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A brief overview of the Technical Sections completed and being worked on for the New Animal Drug Application (NADA) for copper sulfate will be presented. Various aspects of these technical sections will be open for discussion. The update will include information and dates for both the initial labe...

  10. Synthesis and characterization of barium ferrite–silica nanocomposites

    SciTech Connect

    Aguilar-González, M.A.; Mendoza-Suárez, G.; Padmasree, K.P.

    2013-10-15

    In this work, we prepared barium ferrite-silica (BaM-SiO{sub 2}) nanocomposites of different molar ratios by high-energy ball milling, followed by heat-treatment at different temperatures. The microstructure, morphology and magnetic properties were characterized for different synthesis conditions by using X-ray diffraction (XRD), scanning electron microscopy (SEM) and vibrating sample magnetometry (VSM). The results indicate that 15 h of milling was enough to avoid the generation of hematite phase and to get a good dispersion of barium ferrite particles in the ceramic matrix. For milling periods beyond 15 h and heat treatment above 900 °C, the XRD patterns showed the presence of hematite phase caused by the decomposition of BaM. The agglomerate size observed through SEM analysis was around 150 nm with a good BaM dispersion into the SiO{sub 2} matrix. The highest saturation magnetization (Ms) value obtained was 43 emu/g and the corresponding coercivity (Hc) value of 3.4 kOe for the composition 60BaM-40SiO{sub 2} milled for 15 h and heat treated at 900 °C. This coercivity value is acceptable for the application in magnetic recording media. Highlights: • Barium ferrite–silica nanocomposites were prepared by high energy ball milling. • Optimal processing time is 15 h milling and heat treatment at 900 °C. • This is enough to avoid the generation of hematite phase. • Obtain good dispersion of barium ferrite particles in the ceramic matrix • Above this processing time shows the presence of increased amount of hematite.

  11. Time constraints on sulfate-related diagenesis, Capitan Reef Complex, west Texas and New Mexico

    SciTech Connect

    Darke, G. ); Harwood, G. )

    1990-05-01

    Petrographic, paleomagnetic, and outcrop studies of the middle Capitan Reef Complex in the Guadalupe Mountains have provided time constraints on diagenetic events and demonstrated the crucial role of calcium sulfate. Sulfate emplacement occurred at an early stage. The sulfate emplacement post-dated and replaced syndepositional marine margins and lath forms demonstrate replacement was by anhydrite rather then gypsum. Fabric-selective dolomitization and kaolinite precipitation derived from reworking shelf evaporite sequences moving downdip during early stages of drawdown within the Delaware basin. A second period of brine migration causing sulfate emplacement and dolomitization, occurred as the Delaware basin gradually filled with the Castile evaporites, when all remaining porosity within the Capitan shelf margin became indurated by calcium sulfate-laden fluids. This caused pervasive dolomitization, particularly in the lower foreslope, with formation of dolomite rhombs and overgrowths on earlier dolomitized marine cements, coeval with replacive clusters of anhydrite. Most porosity was plugged, some with syndepositional marine cements, but the greater proportion with evaporites until uplift in the Tertiary. Then a meteoric groundwater system became established with subsequent sulfate dissolution. Minor sulfate reduction formed iron sulfides. This oxidized to hematite, which was enclosed within a first generation of zoned calcite spar along some pore margins. Most hematite has a paleomagnetic age of 20 Ma, although minor hematite formation continues to the present. A second, also zoned, coarser calcite spar generation was followed by the latest nonluminescent calcite spar. These calcite spars form the vast bulk of that visible at outcrop.

  12. The Tordo 1 polar cusp barium plasma injection experiment

    NASA Technical Reports Server (NTRS)

    Wescott, E. M.; Stenbaek-Nielsen, H. C.; Davis, T. N.; Jeffries, R. A.; Roach, W. H.

    1978-01-01

    In January 1975, two barium plasma injection experiments were carried out with rockets launched into the upper atmosphere where field lines from the dayside cusp region intersect the ionosphere. The Tordo 1 experiment took place near the beginning of a worldwide magnetic storm. It became a polar cap experiment almost immediately as convection perpendicular to the magnetic field moved the fluorescent plasma jet away from the cusp across the polar cap in an antisunward direction. Convection across the polar cap with an average velocity of more than 1 km/s was observed for nearly 40 min until the barium flux tubes encountered large electron fields associated with a poleward bulge of the auroral oval near Greenland. Prior to the encounter with the aurora near Greenland there is evidence of upward acceleration of the barium ions while they were in the polar cap. The three-dimensional observations of the plasma orientation and motion give an insight into convection from the cusp region across the polar cap, the orientation of the polar cap magnetic field lines out to several earth radii, the causes of polar cap magnetic perturbations, and parallel acceleration processes.

  13. Barium and Tc-poor S stars: Binary masqueraders among carbon stars

    E-print Network

    A. Jorissen; S. Van Eck

    1997-08-06

    The current understanding of the origin of barium and S stars is reviewed, based on new orbital elements and binary frequencies. The following questions are addressed: (i) Is binarity a necessary condition to produce a barium star? (ii) What is the mass transfer mode (wind accretion or RLOF?) responsible for their formation? (iii) Do barium stars form as dwarfs or as giants? (iv) Do barium stars evolve into Tc-poor S stars? (v) What is the relative frequency of Tc-rich and Tc-poor S stars?

  14. Prompt striations observed in a barium thermite release at 335 km

    SciTech Connect

    Simons, D.J.; Pongratz, M.B.; Smith, G.M.; Barasch, G.E.; Fitzgerald, T.J.

    1981-03-01

    Three barium clouds have been released from a single rocket at altitudes of 335, 443, and 535 km. The releases were by means of barium thermite injection. Adding the different cross-field velocity components of the rocket at each of the releases resulted in barium clouds with different kinetic velocity distributions. The barium cloud with the most peaked velocity distribution striated promptly, in good agreement with theoretical predictions based on a kinetic plasma instability. Details of the data analysis and experiment are discussed.

  15. 21 CFR 582.5461 - Manganese sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5461 Manganese sulfate. (a) Product. Manganese sulfate. (b) Conditions of use....

  16. 21 CFR 582.5230 - Calcium sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5230 Calcium sulfate. (a) Product. Calcium sulfate. (b) Conditions of use. This...

  17. 21 CFR 582.5315 - Ferrous sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5315 Ferrous sulfate. (a) Product. Ferrous sulfate. (b) Conditions of use. This...

  18. 21 CFR 582.5230 - Calcium sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5230 Calcium sulfate. (a) Product. Calcium sulfate. (b) Conditions of use. This...

  19. 21 CFR 582.5315 - Ferrous sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5315 Ferrous sulfate. (a) Product. Ferrous sulfate. (b) Conditions of use. This...

  20. 21 CFR 582.5461 - Manganese sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5461 Manganese sulfate. (a) Product. Manganese sulfate. (b) Conditions of use....

  1. 21 CFR 582.5461 - Manganese sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5461 Manganese sulfate. (a) Product. Manganese sulfate. (b) Conditions of use....

  2. 21 CFR 582.5997 - Zinc sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5997 Zinc sulfate. (a) Product. Zinc sulfate. (b) Conditions of use. This...

  3. 21 CFR 582.5443 - Magnesium sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5443 Magnesium sulfate. (a) Product. Magnesium sulfate. (b) Conditions of use....

  4. 21 CFR 582.5230 - Calcium sulfate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5230 Calcium sulfate. (a) Product. Calcium sulfate. (b) Conditions of use....

  5. 21 CFR 582.5461 - Manganese sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5461 Manganese sulfate. (a) Product. Manganese sulfate. (b) Conditions of use....

  6. 21 CFR 582.5230 - Calcium sulfate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5230 Calcium sulfate. (a) Product. Calcium sulfate. (b) Conditions of use....

  7. 21 CFR 184.1315 - Ferrous sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... O, CAS Reg. No. 7782-63-0) is prepared by the action of sulfuric acid on iron. It occurs as pale, bluish-green crystals or granules. Progressive heating of ferrous sulfate heptahydrate produces ferrous sulfate (dried). Ferrous...

  8. Diel cycles in dissolved barium, lead, iron, vanadium, and nitrite in a stream draining a former zinc smelter site near Hegeler, Illinois

    USGS Publications Warehouse

    Kay, R.T.; Groschen, G.E.; Cygan, G.; Dupre, David H.

    2011-01-01

    Diel variations in the concentrations of a number of constituents have the potential to substantially affect the appropriate sampling regimen in acidic streams. Samples taken once during the course of the day cannot adequately reflect diel variations in water quality and may result in an inaccurate understanding of biogeochemical processes, ecological conditions, and of the threat posed by the water to human health and the associated wildlife. Surface water and groundwater affected by acid drainage were sampled every 60 to 90. min over a 48-hour period at a former zinc smelter known as the Hegeler Zinc Superfund Site, near Hegeler, Illinois. Diel variations related to water quality in the aquifer were not observed in groundwater. Diel variations were observed in the temperature, pH, and concentration of dissolved oxygen, nitrite, barium, iron, lead, vanadium, and possibly uranium in surface water. Temperature, dissolved oxygen, nitrite, barium, lead, and uranium generally attained maximum values during the afternoon and minimum values during the night. Iron, vanadium, and pH generally attained minimum values during the afternoon and maximum values during the night. Concentrations of dissolved oxygen were affected by the intensity of photosynthetic activity and respiration, which are dependent upon insolation. Nitrite, an intermediary in many nitrogen reactions, may have been formed by the oxidation of ammonium by dissolved oxygen and converted to other nitrogen species as part of the decomposition of organic matter. The timing of the pH cycles was distinctly different from the cycles found in Midwestern alkaline streams and likely was the result of the photoreduction of Fe3+ to Fe 2+ and variations in the intensity of precipitation of hydrous ferric oxide minerals. Diel cycles of iron and vanadium also were primarily the result of variations in the intensity of precipitation of hydrous ferric oxide minerals. The diel variation in the concentrations of lead, uranium, and barium may have been affected by competition with Fe+2 for sorption sites on hydrous ferric oxide minerals. ?? 2010.

  9. 21 CFR 184.1261 - Copper sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Copper sulfate. 184.1261 Section 184.1261 Food and... Substances Affirmed as GRAS § 184.1261 Copper sulfate. (a) Copper sulfate (cupric sulfate, CuSO4·5H2O, CAS... the reaction of sulfuric acid with cupric oxide or with copper metal. (b) The ingredient must be of...

  10. Cloud and Precipitation Radar

    NASA Astrophysics Data System (ADS)

    Hagen, Martin; Höller, Hartmut; Schmidt, Kersten

    Precipitation or weather radar is an essential tool for research, diagnosis, and nowcasting of precipitation events like fronts or thunderstorms. Only with weather radar is it possible to gain insights into the three-dimensional structure of thunderstorms and to investigate processes like hail formation or tornado genesis. A number of different radar products are available to analyze the structure, dynamics and microphysics of precipitation systems. Cloud radars use short wavelengths to enable detection of small ice particles or cloud droplets. Their applications differ from weather radar as they are mostly orientated vertically, where different retrieval techniques can be applied.

  11. Antarctic polar stratospheric aerosols: The roles of nitrates, chlorides and sulfates

    NASA Technical Reports Server (NTRS)

    Pueschel, R. F.; Snetsinger, K. G.; Goodman, J. K.; Ferry, G. V.; Oberbeck, V. R.; Verma, S.; Fong, W.

    1988-01-01

    Nitric and hydrochloric acids have been postulated to condense in the winter polar stratosphere to become an important component of polar stratospheric clouds. One implication is that the removal of NO(y) from the gas phase by this mechanism allows high Cl(x) concentrations to react with O3, because the formation of ClNO3 is inhibited. Contributions of NO3 and Cl to the stratospheric aerosol were determined during the 1987 Airborne Antarctic Ozone Experiment by testing for the presence of nitrates and chlorides in the condensed phase. Aerosol particles were collected on four 500 micron diameter gold wires, each pretreated differently to give results that were specific to certain physical and chemical aerosol properties. One wire was carbon-coated for concentration and size analyses by scanning electron microscopy; X-ray energy dispersive analyses permitted the detection of S and Cl in individual particles. Three more wires were coated with Nitron, barium chloride and silver nitrate, respectively, to detect nitrate, sulfate and chloride in aerosol particles. All three ions, viz., sulfates, nitrates and chlorides were detected in the Antarctic stratospheric aerosol. In terms of number concentrations, the aerosol was dominated by sulfates, followed by chlorides and nitrates. An inverse linear regression can be established between nitrate concentrations and ozone mixing ratio, and between temperature and nitrates.

  12. Volumetric determination of uranium using titanous sulfate as reductant before oxidimetric titration

    USGS Publications Warehouse

    Wahlberg, James S.; Skinner, Dwight L.; Rader, Lewis F.

    1956-01-01

    A new method for determining uranium in samples containing 0.05 percent or more U3O8, using titanous sulfate as reducing agent, is much shorter, faster, and has fewer interferences than conventional methods using reductor columns. The sample is dissolved with sulfuric, nitric, perchloric, and hydrofluoric acids. Elements that would otherwise form insoluble fluorides are kept in solution by complexing the fluoride ion with boric acid. A precipitation is made with cupferron to remove interfering elements. The solution is filtered to remove the precipitated cupferrates instead of extracting them with chloroform as is usually done. Filtration is preferred to extraction because any niobium that may be in solution forms an insoluble cupferrate that may be removed by filtering but is very difficult to extract with chloroform. Excess cupferron is destroyed by oxidizing with nitric and perchloric acids, and evaporating to dense fumes of sulfuric acid. The uranium is reduced to U(IV) by the addition of titanous sulfate, with cupric sulfate used as an indicator of the completeness of the reduction. Metallic copper is formed when all the uranium is reduced. The reduced copper is then reoxidized by the addition of mercuric perchlorate, an excess of ferric sulfate added, and the solution titrated immediately with standard ceric sulfate with ferroin as an indicator. Precision of the method compared favorable with methods in common use, both for uranium ores and for most types of uranium-rich materials.

  13. 21 CFR 186.1797 - Sodium sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Sodium sulfate. 186.1797 Section 186.1797 Food and... Substances Affirmed as GRAS § 186.1797 Sodium sulfate. (a) Sodium sulfate (Na2SO4, CAS Reg. No. 7757-82-6... crystalline powder. It is prepared by the neutralization of sulfuric acid with sodium hydroxide. (b)...

  14. 21 CFR 186.1797 - Sodium sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Sodium sulfate. 186.1797 Section 186.1797 Food and....1797 Sodium sulfate. (a) Sodium sulfate (Na2SO4, CAS Reg. No. 7757-82-6), also known as Glauber's salt... by the neutralization of sulfuric acid with sodium hydroxide. (b) The ingredient is used as...

  15. 21 CFR 186.1797 - Sodium sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Sodium sulfate. 186.1797 Section 186.1797 Food and... Substances Affirmed as GRAS § 186.1797 Sodium sulfate. (a) Sodium sulfate (Na2SO4, CAS Reg. No. 7757-82-6... crystalline powder. It is prepared by the neutralization of sulfuric acid with sodium hydroxide. (b)...

  16. 21 CFR 186.1797 - Sodium sulfate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Sodium sulfate. 186.1797 Section 186.1797 Food and... Substances Affirmed as GRAS § 186.1797 Sodium sulfate. (a) Sodium sulfate (Na2SO4, CAS Reg. No. 7757-82-6... crystalline powder. It is prepared by the neutralization of sulfuric acid with sodium hydroxide. (b)...

  17. 21 CFR 186.1797 - Sodium sulfate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Sodium sulfate. 186.1797 Section 186.1797 Food and... Substances Affirmed as GRAS § 186.1797 Sodium sulfate. (a) Sodium sulfate (Na2SO4, CAS Reg. No. 7757-82-6... crystalline powder. It is prepared by the neutralization of sulfuric acid with sodium hydroxide. (b)...

  18. 21 CFR 184.1315 - Ferrous sulfate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... Specific Substances Affirmed as GRAS § 184.1315 Ferrous sulfate. (a) Ferrous sulfate heptahydrate (iron (II... iron. It occurs as pale, bluish-green crystals or granules. Progressive heating of ferrous sulfate... nutrient supplements as defined in § 170.3(o)(20) of this chapter and as a processing aid as defined...

  19. 21 CFR 184.1315 - Ferrous sulfate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... Specific Substances Affirmed as GRAS § 184.1315 Ferrous sulfate. (a) Ferrous sulfate heptahydrate (iron (II... iron. It occurs as pale, bluish-green crystals or granules. Progressive heating of ferrous sulfate... nutrient supplements as defined in § 170.3(o)(20) of this chapter and as a processing aid as defined...

  20. 21 CFR 184.1315 - Ferrous sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... GRAS § 184.1315 Ferrous sulfate. (a) Ferrous sulfate heptahydrate (iron (II) sulfate heptahydrate, FeSO4·7H2O, CAS Reg. No. 7782-63-0) is prepared by the action of sulfuric acid on iron. It occurs as..._locations.html. (c) In accordance with § 184.1(b)(1), the ingredients are used in food as...

  1. 21 CFR 184.1315 - Ferrous sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... Specific Substances Affirmed as GRAS § 184.1315 Ferrous sulfate. (a) Ferrous sulfate heptahydrate (iron (II... iron. It occurs as pale, bluish-green crystals or granules. Progressive heating of ferrous sulfate... nutrient supplements as defined in § 170.3(o)(20) of this chapter and as a processing aid as defined...

  2. 21 CFR 556.300 - Gentamicin sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Gentamicin sulfate. 556.300 Section 556.300 Food... Tolerances for Residues of New Animal Drugs § 556.300 Gentamicin sulfate. (a) A tolerance of 0.1 part per million is established for negligible residues of gentamicin sulfate in the uncooked edible tissues...

  3. 21 CFR 556.300 - Gentamicin sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Gentamicin sulfate. 556.300 Section 556.300 Food... Tolerances for Residues of New Animal Drugs § 556.300 Gentamicin sulfate. (a) A tolerance of 0.1 part per million is established for negligible residues of gentamicin sulfate in the uncooked edible tissues...

  4. 21 CFR 556.300 - Gentamicin sulfate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Gentamicin sulfate. 556.300 Section 556.300 Food... Tolerances for Residues of New Animal Drugs § 556.300 Gentamicin sulfate. (a) A tolerance of 0.1 part per million is established for negligible residues of gentamicin sulfate in the uncooked edible tissues...

  5. 21 CFR 556.300 - Gentamicin sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Gentamicin sulfate. 556.300 Section 556.300 Food... Tolerances for Residues of New Animal Drugs § 556.300 Gentamicin sulfate. (a) A tolerance of 0.1 part per million is established for negligible residues of gentamicin sulfate in the uncooked edible tissues...

  6. 21 CFR 556.300 - Gentamicin sulfate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Gentamicin sulfate. 556.300 Section 556.300 Food... Tolerances for Residues of New Animal Drugs § 556.300 Gentamicin sulfate. (a) A tolerance of 0.1 part per million is established for negligible residues of gentamicin sulfate in the uncooked edible tissues...

  7. 21 CFR 582.5443 - Magnesium sulfate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Magnesium sulfate. 582.5443 Section 582.5443 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Supplements 1 § 582.5443 Magnesium sulfate. (a) Product. Magnesium sulfate. (b) Conditions of use....

  8. 21 CFR 582.5443 - Magnesium sulfate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Magnesium sulfate. 582.5443 Section 582.5443 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Supplements 1 § 582.5443 Magnesium sulfate. (a) Product. Magnesium sulfate. (b) Conditions of use....

  9. 21 CFR 582.5443 - Magnesium sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Magnesium sulfate. 582.5443 Section 582.5443 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Supplements 1 § 582.5443 Magnesium sulfate. (a) Product. Magnesium sulfate. (b) Conditions of use....

  10. 21 CFR 184.1443 - Magnesium sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Magnesium sulfate. 184.1443 Section 184.1443 Food... Specific Substances Affirmed as GRAS § 184.1443 Magnesium sulfate. (a) Magnesium sulfate (MgSO4·7H2O, CAS... magnesium oxide, hydroxide, or carbonate with sulfuric acid and evaporating the solution to...

  11. 21 CFR 184.1443 - Magnesium sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Magnesium sulfate. 184.1443 Section 184.1443 Food... Specific Substances Affirmed as GRAS § 184.1443 Magnesium sulfate. (a) Magnesium sulfate (MgSO4·7H2O, CAS... magnesium oxide, hydroxide, or carbonate with sulfuric acid and evaporating the solution to...

  12. 21 CFR 184.1443 - Magnesium sulfate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Magnesium sulfate. 184.1443 Section 184.1443 Food... Specific Substances Affirmed as GRAS § 184.1443 Magnesium sulfate. (a) Magnesium sulfate (MgSO4·7H2O, CAS... magnesium oxide, hydroxide, or carbonate with sulfuric acid and evaporating the solution to...

  13. 21 CFR 582.5443 - Magnesium sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Magnesium sulfate. 582.5443 Section 582.5443 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Supplements 1 § 582.5443 Magnesium sulfate. (a) Product. Magnesium sulfate. (b) Conditions of use....

  14. 21 CFR 582.5443 - Magnesium sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Magnesium sulfate. 582.5443 Section 582.5443 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Supplements 1 § 582.5443 Magnesium sulfate. (a) Product. Magnesium sulfate. (b) Conditions of use....

  15. 21 CFR 184.1443 - Magnesium sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Magnesium sulfate. 184.1443 Section 184.1443 Food... GRAS § 184.1443 Magnesium sulfate. (a) Magnesium sulfate (MgSO4·7H2O, CAS Reg. No. 10034-99-8) occurs naturally as the mineral epsomite. It is prepared by neutralization of magnesium oxide, hydroxide,...

  16. 21 CFR 184.1443 - Magnesium sulfate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Magnesium sulfate. 184.1443 Section 184.1443 Food... Specific Substances Affirmed as GRAS § 184.1443 Magnesium sulfate. (a) Magnesium sulfate (MgSO4·7H2O, CAS... magnesium oxide, hydroxide, or carbonate with sulfuric acid and evaporating the solution to...

  17. 21 CFR 182.1125 - Aluminum sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Aluminum sulfate. 182.1125 Section 182.1125 Food... GENERALLY RECOGNIZED AS SAFE Multiple Purpose GRAS Food Substances § 182.1125 Aluminum sulfate. (a) Product. Aluminum sulfate. (b) Conditions of use. This substance is generally recognized as safe when used...

  18. 21 CFR 182.1125 - Aluminum sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Aluminum sulfate. 182.1125 Section 182.1125 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR... Substances § 182.1125 Aluminum sulfate. (a) Product. Aluminum sulfate. (b) Conditions of use. This...

  19. 21 CFR 182.1125 - Aluminum sulfate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Aluminum sulfate. 182.1125 Section 182.1125 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR... Substances § 182.1125 Aluminum sulfate. (a) Product. Aluminum sulfate. (b) Conditions of use. This...

  20. 21 CFR 182.1125 - Aluminum sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Aluminum sulfate. 182.1125 Section 182.1125 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR... Substances § 182.1125 Aluminum sulfate. (a) Product. Aluminum sulfate. (b) Conditions of use. This...

  1. 21 CFR 182.1125 - Aluminum sulfate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Aluminum sulfate. 182.1125 Section 182.1125 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR... Substances § 182.1125 Aluminum sulfate. (a) Product. Aluminum sulfate. (b) Conditions of use. This...

  2. 21 CFR 582.1125 - Aluminum sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Aluminum sulfate. 582.1125 Section 582.1125 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1125 Aluminum sulfate. (a) Product. Aluminum sulfate. (b) Conditions of use. This...

  3. 21 CFR 582.1125 - Aluminum sulfate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Aluminum sulfate. 582.1125 Section 582.1125 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1125 Aluminum sulfate. (a) Product. Aluminum sulfate. (b) Conditions of use. This...

  4. 21 CFR 582.1125 - Aluminum sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Aluminum sulfate. 582.1125 Section 582.1125 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1125 Aluminum sulfate. (a) Product. Aluminum sulfate. (b) Conditions of use. This...

  5. 21 CFR 582.1125 - Aluminum sulfate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Aluminum sulfate. 582.1125 Section 582.1125 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1125 Aluminum sulfate. (a) Product. Aluminum sulfate. (b) Conditions of use. This...

  6. 21 CFR 582.1125 - Aluminum sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Aluminum sulfate. 582.1125 Section 582.1125 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1125 Aluminum sulfate. (a) Product. Aluminum sulfate. (b) Conditions of use. This...

  7. 21 CFR 182.8997 - Zinc sulfate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Zinc sulfate. 182.8997 Section 182.8997 Food and... CONSUMPTION (CONTINUED) SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients § 182.8997 Zinc sulfate. (a) Product. Zinc sulfate. (b) Conditions of use. This substance is generally recognized as safe when used...

  8. 21 CFR 582.5997 - Zinc sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Zinc sulfate. 582.5997 Section 582.5997 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS... 1 § 582.5997 Zinc sulfate. (a) Product. Zinc sulfate. (b) Conditions of use. This substance...

  9. 21 CFR 582.5997 - Zinc sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Zinc sulfate. 582.5997 Section 582.5997 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS... 1 § 582.5997 Zinc sulfate. (a) Product. Zinc sulfate. (b) Conditions of use. This substance...

  10. 21 CFR 182.8997 - Zinc sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Zinc sulfate. 182.8997 Section 182.8997 Food and... CONSUMPTION (CONTINUED) SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients § 182.8997 Zinc sulfate. (a) Product. Zinc sulfate. (b) Conditions of use. This substance is generally recognized as safe when used...

  11. 21 CFR 582.5997 - Zinc sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Zinc sulfate. 582.5997 Section 582.5997 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS... 1 § 582.5997 Zinc sulfate. (a) Product. Zinc sulfate. (b) Conditions of use. This substance...

  12. 21 CFR 182.8997 - Zinc sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Zinc sulfate. 182.8997 Section 182.8997 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients § 182.8997 Zinc sulfate. (a) Product. Zinc sulfate. (b) Conditions...

  13. 21 CFR 582.5997 - Zinc sulfate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Zinc sulfate. 582.5997 Section 582.5997 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS... 1 § 582.5997 Zinc sulfate. (a) Product. Zinc sulfate. (b) Conditions of use. This substance...

  14. 21 CFR 182.8997 - Zinc sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Zinc sulfate. 182.8997 Section 182.8997 Food and... CONSUMPTION (CONTINUED) SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients § 182.8997 Zinc sulfate. (a) Product. Zinc sulfate. (b) Conditions of use. This substance is generally recognized as safe when used...

  15. 21 CFR 182.8997 - Zinc sulfate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Zinc sulfate. 182.8997 Section 182.8997 Food and... CONSUMPTION (CONTINUED) SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients § 182.8997 Zinc sulfate. (a) Product. Zinc sulfate. (b) Conditions of use. This substance is generally recognized as safe when used...

  16. 21 CFR 582.5997 - Zinc sulfate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Zinc sulfate. 582.5997 Section 582.5997 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS... 1 § 582.5997 Zinc sulfate. (a) Product. Zinc sulfate. (b) Conditions of use. This substance...

  17. Reduction of Np(V) and precipitation of Np(IV) by an anaerobic microbial consortium.

    PubMed

    Rittmann, Bruce E; Banaszak, James E; Reed, Donald T

    2002-01-01

    A combination of experimental, analytical, and modeling investigations shows that an anaerobic, sulfate-reducing consortium reduced Np(V) to Np(IV), with subsequent precipitation of a Np(IV) solid. Precipitation of Np(IV) during growth on pyruvate occurred before sulfate reduction began. H2 stimulated precipitation of Np(IV) when added alone to growing cells, but it slowed precipitation when added along with pyruvate. Increasing concentrations of pyruvate also retarded precipitation. Accumulation of an intermediate pyruvate-fermentation product--probably succinate--played a key role in retarding Np(IV) precipitation by complexing the Np(IV). Hydrogen appears to have two roles in controlling Np precipitation: donating electrons for Np(V) reduction and modulating intermediate levels. That Np(V) is microbially reduced and subsequently precipitated under anaerobic conditions has likely beneficial implications for the containment of Np on lands contaminated by radionuclides, but complexation by fermentation intermediates can prevent immobilization by precipitation. PMID:12688585

  18. Crystallization of Chicken Egg White Lysozyme from Assorted Sulfate Salts

    NASA Technical Reports Server (NTRS)

    Forsythe, Elizabeth L.; Snell, Edward H.; Malone, Christine C.; Pusey, Marc L.

    1998-01-01

    Chicken egg white lysozyme has been found to crystallize from ammonium, sodium, potassium, rubidium, magnesium, and manganese sulfates at acidic and basic pH, with protein concentrations from 60 to 190 mg/ml. Four different crystal morphologies have been obtained, depending upon the temperature, protein concentration, and precipitating salt employed, Crystals grown at 15 C were generally tetragonal, with space group P43212. Crystallization at 20 C typically resulted in the formation of orthorhombic crystals, space group P21212 1. The tetragonal much less than orthorhombic morphology transition appeared to be a function of both the temperature and protein concentration, occurring between 15 and 20 C and between 100 and 125 mg/ml protein concentration. Crystallization from 0.8 -1.2M magnesium sulfate at pH 7.6 - 8.0 gave a hexagonal (trigonal) crystal form, space group P3121, which diffracted to 2.8 A. Ammonium sulfate was also found to result in a monoclinic form, space group C2. Small twinned monoclinic crystals of approx. 0.2 mm on edge were grown by dialysis followed by seeded sitting drop crystallization.

  19. Conversion of alkali metal sulfate to the carbonate

    DOEpatents

    Sheth, Atul C. (Woodridge, IL)

    1982-01-01

    A process for converting potassium sulfate to potassium carbonate in which a mixture of potassium sulfate and calcium oxide are reacted at a temperature in the range of between about 700.degree. C. and about 800.degree. C. with a gaseous mixture having a minor amount of hydrogen and/or carbon monoxide in a diluent with the calcium oxide being present in an amount not greater than about 20 percent by weight of the potassium sulfate to produce an aqueous mixture of potassium sulfide, potassium bisulfide, potassium hydroxide and calcium sulfide and a gaseous mixture of steam and hydrogen sulfide. The potassium and calcium salts are quenched to produce an aqueous slurry of soluble potassium salts and insoluble calcium salts and a gaseous mixture of steam and hydrogen sulfide. The insoluble calcium salts are then separated from the aqueous solution of soluble potassium salts. The calcium salts are dried to produce calcium sulfide, calcium bisulfide and steam, and then, the calcium sulfide and calcium bisulfide are converted to the oxide and recycled. The soluble potassium salts are carbonated to produce potassium carbonate which is concentrated and the precipitated crystals separated. The sulfur-containing compounds are further treated.

  20. Is extreme precipitation changing?

    NASA Astrophysics Data System (ADS)

    Papalexiou, Simon Michael

    2015-04-01

    For most of the scientists climate change is a fact. Climate change implies changes not only on the behavior of the temperature but also on other climatic variables like the precipitation. The question raised in this study is whether or not the annual daily maximum precipitation has changed. In order to evaluate if this question can be answered, several thousands of precipitation records are analyzed from all over the globe. Initially the annual daily maxima time series are carefully formed and sequentially all possible trends are estimated in a moving window framework and for several interannual periods, e.g., from 10 years to 100 years. The aim is to estimate the difference between the percentage of increasing and decreasing trends in the annual daily maximum precipitation and assess if this difference indicates any specific pattern.

  1. Map Maker - Precipitation

    USGS Multimedia Gallery

    The National Atlas offered the Federal government's first on-line interactive Map Maker in 1997. A regional map of annual precipitation center on Oregon is shown. This image is simply a screen shot. Its source is listed below....

  2. Precipitation Estimates for Hydroelectricity

    NASA Technical Reports Server (NTRS)

    Tapiador, Francisco J.; Hou, Arthur Y.; de Castro, Manuel; Checa, Ramiro; Cuartero, Fernando; Barros, Ana P.

    2011-01-01

    Hydroelectric plants require precise and timely estimates of rain, snow and other hydrometeors for operations. However, it is far from being a trivial task to measure and predict precipitation. This paper presents the linkages between precipitation science and hydroelectricity, and in doing so it provides insight into current research directions that are relevant for this renewable energy. Methods described include radars, disdrometers, satellites and numerical models. Two recent advances that have the potential of being highly beneficial for hydropower operations are featured: the Global Precipitation Measuring (GPM) mission, which represents an important leap forward in precipitation observations from space, and high performance computing (HPC) and grid technology, that allows building ensembles of numerical weather and climate models.

  3. Chemisorption And Precipitation Reactions

    EPA Science Inventory

    The transport and bioavailability of chemical components within soils is, in part, controlled by partitioning between solids and solution. General terms used to describe these partitioning reactions include chemisorption and precipitation. Chemisorption is inclusive of the suit...

  4. Sulfate ingress in Portland cement

    SciTech Connect

    Lothenbach, Barbara; Bary, Benoit; Le Bescop, Patrick; Leterrier, Nikos

    2010-08-15

    The interaction of mortar with sulfate solutions leads to a reaction front within the porous material and to expansion. Thermodynamic modelling coupled with transport codes was used to predict sulfate ingress. Alternatively, 'pure' thermodynamic models - without consideration of transport - were used as a fast alternative to coupled models: they are more flexible and allow easy parameter variations but the results relate neither to distance nor to time. Both transport and pure thermodynamic modelling gave comparable results and were able to reproduce the changes observed in experiments. The calculated total volume of the solids did not exceed the initial volume of the paste indicating that not the overall volume restriction leads to the observed expansion but rather the formation of ettringite within the matrix and the development of crystallisation pressure in small pores. The calculations indicate that periodic changing of the Na{sub 2}SO{sub 4} solution results in more intense degradation.

  5. Method for magnesium sulfate recovery

    DOEpatents

    Gay, Richard L. (Canoga Park, CA); Grantham, LeRoy F. (Calabasas, CA)

    1987-01-01

    A method of obtaining magnesium sulfate substantially free from radioactive uranium from a slag containing the same and having a radioactivity level of at least about 7000 pCi/gm. The slag is ground to a particle size of about 200 microns or less. The ground slag is then contacted with a concentrated sulfuric acid under certain prescribed conditions to produce a liquid product and a solid product. The particulate solid product and a minor amount of the liquid is then treated to produce a solid residue consisting essentially of magnesium sulfate substantially free of uranium and having a residual radioactivity level of less than 1000 pCi/gm. In accordance with the preferred embodiment of the invention, a catalyst and an oxidizing agent are used during the initial acid treatment and a final solid residue has a radioactivity level of less than about 50 pCi/gm.

  6. Method for magnesium sulfate recovery

    DOEpatents

    Gay, R.L.; Grantham, L.F.

    1987-08-25

    A method is described for obtaining magnesium sulfate substantially free from radioactive uranium from a slag containing the same and having a radioactivity level of at least about 7,000 pCi/gm. The slag is ground to a particle size of about 200 microns or less. The ground slag is then contacted with a concentrated sulfuric acid under certain prescribed conditions to produce a liquid product and a solid product. The particulate solid product and a minor amount of the liquid is then treated to produce a solid residue consisting essentially of magnesium sulfate substantially free of uranium and having a residual radioactivity level of less than 1,000 pCi/gm. In accordance with the preferred embodiment of the invention, a catalyst and an oxidizing agent are used during the initial acid treatment and a final solid residue has a radioactivity level of less than about 50 pCi/gm.

  7. A review of the health impacts of barium from natural and anthropogenic exposure.

    PubMed

    Kravchenko, Julia; Darrah, Thomas H; Miller, Richard K; Lyerly, H Kim; Vengosh, Avner

    2014-08-01

    There is an increasing public awareness of the relatively new and expanded industrial barium uses which are potential sources of human exposure (e.g., a shale gas development that causes an increased awareness of environmental exposures to barium). However, absorption of barium in exposed humans and a full spectrum of its health effects, especially among chronically exposed to moderate and low doses of barium populations, remain unclear. We suggest a systematic literature review (from 1875 to 2014) on environmental distribution of barium, its bioaccumulation, and potential and proven health impacts (in animal models and humans) to provide the information that can be used for optimization of future experimental and epidemiological studies and developing of mitigative and preventive strategies to minimize negative health effects in exposed populations. The potential health effects of barium exposure are largely based on animal studies, while epidemiological data for humans, specifically for chronic low-level exposures, are sparse. The reported health effects include cardiovascular and kidney diseases, metabolic, neurological, and mental disorders. Age, race, dietary patterns, behavioral risks (e.g., smoking), use of medications (those that interfere with absorbed barium in human organism), and specific physiological status (e.g., pregnancy) can modify barium effects on human health. Identifying, evaluating, and predicting the health effects of chronic low-level and moderate-level barium exposures in humans is challenging: Future research is needed to develop an understanding of barium bioaccumulation in order to mitigate its potential health impacts in various exposured populations. Further, while occupationally exposed at-risk populations exist, it is also important to identify potentially vulnerable subgroups among non-occupationally exposed populations (e.g., elderly, pregnant women, children) who are at higher risk of barium exposure from drinking water and food. PMID:24844320

  8. Tungsten and barium transport in the internal plasma of hollow cathodes

    NASA Astrophysics Data System (ADS)

    Polk, James E.; Mikellides, Ioannis G.; Katz, Ira; Capece, Angela M.

    2009-06-01

    The effect of tungsten erosion, transport, and redeposition on the operation of dispenser hollow cathodes was investigated in detailed examinations of the discharge cathode inserts from 8200 h and 30 352 h ion engine wear tests. Erosion and subsequent redeposition of tungsten in the electron emission zone at the downstream end of the insert reduce the porosity of the tungsten matrix, preventing the flow of barium from the interior. This inhibits the interfacial reactions of the barium-calcium-aluminate impregnant with the tungsten in the pores. A numerical model of barium transport in the internal xenon discharge plasma shows that the barium required to reduce the work function in the emission zone can be supplied from upstream through the gas phase. Barium that flows out of the pores of the tungsten insert is rapidly ionized in the xenon discharge and pushed back to the emitter surface by the electric field and drag from the xenon ion flow. This barium ion flux is sufficient to maintain a barium surface coverage at the downstream end greater than 0.6, even if local barium production at that point is inhibited by tungsten deposits. The model also shows that the neutral barium pressure exceeds the equilibrium vapor pressure of the impregnant decomposition reaction over much of the insert length, so the reactions are suppressed. Only a small region upstream of the zone blocked by tungsten deposits is active and supplies the required barium. These results indicate that hollow cathode failure models based on barium depletion rates in vacuum dispenser cathodes are very conservative.

  9. Inhibition of nickel precipitation by organic ligands

    SciTech Connect

    Hu, H.L.; Nikolaidis, N.P.; Grasso, D.

    1996-11-01

    Wastewaters from electroplating are very complex due to the composition of the plating baths. A nickel plating bath typically consists of a nickel source (nickel chloride or nickel sulfate), complexing agents to solubilize nickel ions controlling their concentration in the solution, buffering agents to maintain pH, brighteners to improve brightness of the plated metal, stabilizers (inhibitors) to prevent undesired reactions, accelerators to enhance speed of reactions, wetting agents to reduce surface tension at the metal surface, and reducing agents (only for electroless nickel plating) to supply electrons for reduction of the nickel. Alkaline precipitation is the most common method of recovering nickel from wastewaters. However, organic constituents found in the wastewaters can mask or completely inhibit the precipitation of nickel. The objective of this study was to conduct an equilibrium study to explore the inhibition behavior of various organic ligands on nickel precipitation. This will lay the groundwork for development of technologies efficacious in the treatment of complexed nickel. The organic ligands used in this study are EDTA, triethanolamine (TEA), gluconate, and tartrate.

  10. Chemical quality of precipitation at Greenville, Maine

    USGS Publications Warehouse

    Smath, J.A.; Potter, T.L.

    1987-01-01

    Weekly composite precipitation samples were collected at a rural site located in Greenville, Maine for analysis of trace metals and organic compounds. Samples collected during February 1982, through May 1984, were analyzed for cadmium, chromium, copper, lead, mercury, nickel, and zinc and during February 1982, through March 1983, for chlorinated hydrocarbon pesticides, pthalate ester plasticizers, and polychlorinated biphenyls. Deposition rates were computed. Data reported by the NADP (National Atmospheric Deposition Program) was used to evaluate the general chemical quality of the precipitation. The precipitation had relatively high concentrations of hydrogen ions, sulfate, and nitrate, compared to other constituents. Of the trace metals included for analysis, only copper, lead, and zinc were consistently detected. Lead concentrations exceeded the U.S. EPA recommended limit for domestic water supply in three samples. High deposition rates for some of the metals were episodic. Alpha-hexachlorocyclohexane was the only organic compound that was consistently detected (maximum 120 nanograms/L). None of the other organic compounds were detected in any of the samples. (Author 's abstract)

  11. Sulfate migration in a river affected by acid mine drainage from the Dabaoshan mining area, South China.

    PubMed

    Chen, Meiqin; Lu, Guining; Guo, Chuling; Yang, Chengfang; Wu, Jingxiong; Huang, Weilin; Yee, Nathan; Dang, Zhi

    2015-01-01

    Sulfate, a major component of acid mine drainage (AMD), its migration in an AMD-affected river which located at the Dabaoshan mine area of South China was investigated to pursue the remediation strategy. The existing factors of relatively low pH values of 2.8-3.9, high concentrations of SO4(2-) (?1940 mg L(-1)) and Fe(3+) (?112 mg L(-1)) facilitated the precipitation of schwertmannite (Fe8O8(OH)6SO4·nH2O) in the upstream river. Geochemical model calculations implied the river waters were supersaturated, creating the potential for precipitation of iron oxyhydroxides. These minerals evolved from schwertmannite to goethite with the increasing pH from 2.8 to 5.8 along the river. The concentration of heavy metals in river waters was great reduced as a result of precipitation effects. The large size of the exchangeable sulfate pool suggested that the sediments had a strong capacity to bind SO4(2-). The XRD results indicated that schwertmannite was the predominant form of sulfate-bearing mineral phases, which was likely to act as a major sulfate sink by incorporating water-borne sulfate into its internal structure and adsorbing it onto its surface. The small size of reduced sulfur pools and strong oxidative status in the surface sediments further showed that SO4(2-) shifting from water to sediment in form of sulfate reduction was not activated. In short, precipitation of sulfate-rich iron oxyhydroxides and subsequent SO4(2-) adsorption on these minerals as well as water dilution contributed to the attenuation of SO4(2-) along the river waters. PMID:25189685

  12. Monohydrated Sulfates in Aurorae Chaos

    NASA Technical Reports Server (NTRS)

    2008-01-01

    This image of sulfate-containing deposits in Aurorae Chaos was taken by the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) at 0653 UTC (2:53 a.m. EDT) on June 10, 2007, near 7.5 degrees south latitude, 327.25 degrees east longitude. CRISM's image was taken in 544 colors covering 0.36-3.92 micrometers, and shows features as small as 40 meters (132 feet) across. The region covered is roughly 12 kilometers (7.5 miles) wide at its narrowest point.

    Aurorae Chaos lies east of the Valles Marineris canyon system. Its western edge extends toward Capri and Eos Chasmata, while its eastern edge connects with Aureum Chaos. Some 750 kilometers (466 miles) wide, Aurorae Chaos is most likely the result of collapsed surface material that settled when subsurface ice or water was released.

    The top panel in the montage above shows the location of the CRISM image on a mosaic taken by the Mars Odyssey spacecraft's Thermal Emission Imaging System (THEMIS). The CRISM data covers an area featuring several knobs of erosion-resistant material at one end of what appears to be a large teardrop shaped plateau. Similar plateaus occur throughout the interior of Valles Marineris, and they are formed of younger, typically layered rocks that post-date formation of the canyon system. Many of the deposits contain sulfate-rich layers, hinting at ancient saltwater.

    The center left image, an infrared false color image, reveals a swath of light-colored material draped over the knobs. The center right image unveils the mineralogical composition of the area, with yellow representing monohydrated sulfates (sulfates with one water molecule incorporated into each molecule of the mineral).

    The lower two images are renderings of data draped over topography with 5 times vertical exaggeration. These images provide a view of the topography and reveal how the monohydrated sulfate-containing deposits drape over the knobs and also an outcrop in lower-elevation parts of the plateau.

    CRISM is one of six science instruments on NASA's Mars Reconnaissance Orbiter. Led by The Johns Hopkins University Applied Physics Laboratory, Laurel, Md., the CRISM team includes expertise from universities, government agencies and small businesses in the United States and abroad. NASA's Jet Propulsion Laboratory, a division of the California Institute of Technology in Pasadena, manages the Mars Reconnaissance Orbiter and the Mars Science Laboratory for NASA's Science Mission Directorate, Washington. Lockheed Martin Space Systems, Denver, built the orbiter.

  13. Modeling of Sulfate Double-salts in Nuclear Wastes

    SciTech Connect

    Toghiani, B.

    2000-10-30

    Due to limited tank space at Hanford and Savannah River, the liquid nuclear wastes or supernatants have been concentrated in evaporators to remove excess water prior to the hot solutions being transferred to underground storage tanks. As the waste solutions cooled, the salts in the waste exceeded the associated solubility limits and precipitated in the form of saltcakes. The initial step in the remediation of these saltcakes is a rehydration process called saltcake dissolution. At Hanford, dissolution experiments have been conducted on small saltcake samples from five tanks. Modeling of these experimental results, using the Environmental Simulation Program (ESP), are being performed at the Diagnostic Instrumentation and Analysis Laboratory (DIAL) at Mississippi State University. The River Protection Project (RPP) at Hanford will use these experimental and theoretical results to determine the amount of water that will be needed for its dissolution and retrieval operations. A comprehensive effort by the RPP and the Tank Focus Area continues to validate and improve the ESP and its databases for this application. The initial effort focused on the sodium, fluoride, and phosphate system due to its role in the formation of pipeline plugs. In FY 1999, an evaluation of the ESP predictions for sodium fluoride, trisodium phosphate dodecahydrate, and natrophosphate clearly indicated that improvements to the Public database of the ESP were needed. One of the improvements identified was double salts. The inability of any equilibrium thermodynamic model to properly account for double salts in the system can result in errors in the predicted solid-liquid equilibria (SLE) of species in the system. The ESP code is evaluated by comparison with experimental data where possible. However, data does not cover the range of component concentrations and temperatures found in many tank wastes. Therefore, comparison of ESP with another code is desirable, and may illuminate problems with both. For this purpose, the SOLGASMIX code was used in conjunction with a small private database developed at ORNL. This code calculates thermodynamic equilibria through minimization of Gibbs Energy, and utilizes the Pitzer model for activity coefficients. The sodium nitrate-sulfate double salt and the sodium fluoride-sulfate double salt were selected for the FY 2000 validation study of ESP. Even though ESP does not include the sulfate-nitrate double salt, this study found that this omission does not appear to be a major consequence. In this case, the solubility predictions with and without the sulfate-nitrate double salt are comparable. In contrast, even though the sulfate-fluoride double salt is included within the ESP databank, comparison to previous experimental results indicates that ESP underestimates solubility. Thus, the prediction for the sulfate-fluoride system needs to be improved. A main consequence of the inability to accurately predict the SLE of double salts is its impact on the predicted ionic strength of the solution. The ionic strength has been observed to be an important factor in the formation of pipeline plugs. To improve the ESP prediction, solubility tests on the sulfate-fluoride system are underway at DIAL, and these experimental results will be incorporated into the Public database by OLI System, Inc. Preliminary ESP simulations also indicated difficulties with the SLE prediction for anhydrous sodium sulfate. The Public database for the ESP does not include fundamental parameters for this solid in mixed solutions below 32.4 C. The limitation, in the range of anhydrous sodium sulfate, leads to convergence problems in ESP and to inaccurate predictions of solubility near the invariant point when sodium sulfate decahydrate and other salts, such as sodium nitrate, were present. These difficulties were partially corrected through the use of an additional database. In conclusion, these results indicate the need for experimental data at temperatures above 25 C and in solutions containing both nitrate and hydroxide. Furthermore, the validation and do

  14. Sulfates on Mars: Indicators of Aqueous Processes

    NASA Technical Reports Server (NTRS)

    Bishop, Janice L.; Lane, Melissa D.; Dyar, M. Darby; Brown, Adrian J.

    2006-01-01

    Recent analyses by MER instruments at Meridiani Planum and Gusev crater and the OMEGA instrument on Mars Express have provided detailed information about the presence of sulfates on Mars [1,2,3]. We are evaluating these recent data in an integrated multi-disciplinary study of visible-near-infrared, mid-IR and Mossbauer spectra of several sulfate minerals and sulfate-rich analog sites. Our analyses suggest that hydrated iron sulfates may account for features observed in Mossbauer and mid-IR spectra of Martian soils [4]. The sulfate minerals kieserite, gypsum and other hydrated sulfates have been identified in OMEGA spectra in the layered terrains in Valles Marineris and Terra Meridiani [2]. These recent discoveries emphasize the importance of studying sulfate minerals as tracers of aqueous processes. The sulfate-rich rock outcrops observed in Meridiani Planum may have formed in an acidic environment similar to acid rock drainage environments on Earth [5]. Because microorganisms typically are involved in the oxidation of sulfides to sulfates in terrestrial sites, sulfate-rich rock outcrops on Mars may be a good location to search for evidence of past life on that planet. Whether or not life evolved on Mars, following the trail of sulfate minerals will lead to a better understanding of aqueous processes and chemical weathering.

  15. The effect of barium on perceptions of taste intensity and palatability

    PubMed Central

    Dietsch, Angela M.; Solomon, Nancy Pearl; Steele, Catriona M.; Pelletier, Cathy A.

    2015-01-01

    Purpose Barium may affect the perception of taste intensity and palatability. Such differences are important considerations in the selection of dysphagia assessment strategies and interpretation of results. Methods Eighty healthy women grouped by age (younger, older) and genetic taste status (supertaster, non-taster) rated intensity and palatability for seven tastants prepared in deionized water with and without 40% w/v barium: non-carbonated and carbonated water, diluted ethanol, and high concentrations of citric acid (sour), sodium chloride (salty), caffeine (bitter) and sucrose (sweet). Mixed model analyses explored the effects of barium, taster status, and age on perceived taste intensity and acceptability of stimuli. Results Barium was associated with lower taste intensity ratings for sweet, salty, and bitter tastants, higher taste intensity in carbonated water, and lower palatability in water, sweet, sour, and carbonated water. Older subjects reported lower palatability (all barium samples, sour) and higher taste intensity scores (ethanol, sweet, sour) compared to younger subjects. Supertasters reported higher taste intensity (ethanol, sweet, sour, salty, bitter) and lower palatability (ethanol, salty, bitter) than non-tasters. Refusal rates were highest for younger subjects and supertasters, and for barium (regardless of tastant), bitter, and ethanol. Conclusions Barium suppressed the perceived intensity of some tastes and reduced palatability. These effects are more pronounced in older subjects and supertasters, but younger supertasters are least likely to tolerate trials of barium and strong tastant solutions. PMID:24037100

  16. The effect of barium on perceptions of taste intensity and palatability.

    PubMed

    Dietsch, Angela M; Solomon, Nancy Pearl; Steele, Catriona M; Pelletier, Cathy A

    2014-02-01

    Barium may affect the perception of taste intensity and palatability. Such differences are important considerations in the selection of dysphagia assessment strategies and interpretation of results. Eighty healthy women grouped by age (younger, older) and genetic taste status (supertaster, nontaster) rated intensity and palatability for seven tastants prepared in deionized water with and without 40 % w/v barium: noncarbonated and carbonated water, diluted ethanol, and high concentrations of citric acid (sour), sodium chloride (salty), caffeine (bitter), and sucrose (sweet). Mixed-model analyses explored the effects of barium, taster status, and age on perceived taste intensity and acceptability of stimuli. Barium was associated with lower taste intensity ratings for sweet, salty, and bitter tastants, higher taste intensity in carbonated water, and lower palatability in water, sweet, sour, and carbonated water. Older subjects reported lower palatability (all barium samples, sour) and higher taste intensity scores (ethanol, sweet, sour) compared to younger subjects. Supertasters reported higher taste intensity (ethanol, sweet, sour, salty, bitter) and lower palatability (ethanol, salty, bitter) than nontasters. Refusal rates were highest for younger subjects and supertasters, and for barium (regardless of tastant), bitter, and ethanol. Barium suppressed the perceived intensity of some tastes and reduced palatability. These effects are more pronounced in older subjects and supertasters, but younger supertasters are least likely to tolerate trials of barium and strong tastant solutions. PMID:24037100

  17. 75 FR 36629 - Barium Chloride From the People's Republic of China: Continuation of Antidumping Duty Order

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-06-28

    ... Barium Chloride From China, 75 FR 33824 (June 15, 2010), and Barium Chloride from China (Inv. No. 731-TA... Five-year (``Sunset'') Review, 74 FR 31412 (July 1, 2009). As a result of its review, the Department... China: Final Results of Expedited Third Sunset Review of Antidumping Duty Order, 74 FR 55814 (October...

  18. 75 FR 36629 - Barium Chloride From the People's Republic of China: Continuation of Antidumping Duty Order

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-06-28

    ... Five-year (``Sunset'') Review, 74 FR 31412 (July 1, 2009). As a result of its review, the Department... China: Final Results of Expedited Third Sunset Review of Antidumping Duty Order, 74 FR 55814 (October 29... Barium Chloride From China, 75 FR 33824 (June 15, 2010), and Barium Chloride from China (Inv. No....

  19. SHORT TERM TOXICITY (1 AND 10 DAY GAVAGE) OF BARIUM CHLORIDE IN MALE AND FEMALE RATS

    EPA Science Inventory

    To assess adverse effects that might be caused by an event resulting in high levels of barium in drinking water, rats were gavaged with barium chloride (BaCl2 at dosage levels of 30,100, and 300 rng/kg in a 1-day study and at 100,145,209, and 300 rng/kg for 10 days, and the effec...

  20. Impact of thermal strain on the dielectric constant of sputtered barium strontium titanate thin films

    E-print Network

    York, Robert A.

    Impact of thermal strain on the dielectric constant of sputtered barium strontium titanate thin, California 93106 Received 6 November 2001; accepted for publication 10 January 2002 Barium strontium titanate: magnesium oxide, strontium titanate, sapphire, silicon, and vycor glass. These substrates were chosen

  1. Dielectric properties of MgO-doped compositionally graded multilayer barium strontium titanate films

    E-print Network

    Alpay, S. Pamir

    Dielectric properties of MgO-doped compositionally graded multilayer barium strontium titanate shifters and filters operat- ing in the microwave regime.1­4 Ferroelectrics FEs such as barium strontium in monolithic BST films especially with low strontium content, although the addition of MgO causes a reduction

  2. Microwave dielectric properties of graded barium strontium titanate films M. W. Cole,1,a

    E-print Network

    Alpay, S. Pamir

    Microwave dielectric properties of graded barium strontium titanate films M. W. Cole,1,a C. V strontium titanate BaxSr1-xTiO3 or BST multilayers 5 mol % MgO doped and undoped were prepared via metallo, delay lines, filters, and phase shifters for steerable antennas.1­3 Barium strontium titanate BaxSr1-x

  3. LACK OF EFFECT OF DRINKING WATER BARIUM ON CARDIOVASCULAR RISK FACTORS

    EPA Science Inventory

    Higher cardiovascular mortality has been associated in a single epidemiological study with higher levels of barium in drinking water. he purpose of this study was to determine whether drinking water barium at levels found in some U.S. communities alters the known risk factors for...

  4. Evidence against Barium in the Mushroom Trogia venenata as a Cause of Sudden Unexpected Deaths in Yunnan, China

    PubMed Central

    Zhang, Ying; Li, Yanchun; Wu, Gang; Feng, Bang; Yoell, Shanze; Yu, Zefen; Zhang, Keqin

    2012-01-01

    This study examined barium concentrations in the mushroom Trogia venenata, the leading culprit for sudden unexpected deaths in Yunnan, southwest China. We found that barium concentrations in T. venenata from Yunnan were low and comparable to other foods, inconsistent with barium concentrations in this mushroom as a significant contributor to these deaths. PMID:23042168

  5. doi:10.1016/j.gca.2004.11.026 Barium uptake and adsorption in diatoms

    E-print Network

    Morel, François M. M.

    doi:10.1016/j.gca.2004.11.026 Barium uptake and adsorption in diatoms ERIKA STERNBERG,1, *, DEGUI) Abstract--Using trace metal-defined culture conditions, we measured the cellular barium concentration and Dahmke, 1994) and the flux of particulate biogenic barium correlates well with the flux of organic carbon

  6. Nanoshell tubes of ferroelectric lead zirconate titanate and barium titanate Yun Luo, Izabela Szafraniak, and Nikolai D. Zakharov

    E-print Network

    Ramesh, R.

    Nanoshell tubes of ferroelectric lead zirconate titanate and barium titanate Yun Luo, Izabela templates, barium titanate and lead zirconate titanate tubes with diameters ranging from 50 nm up to several (PbZr0.52Ti0.48O3 ,PZT) and barium titanate (BaTiO3 ,BTO) nanotubes were fabricated by using

  7. Barium Ions for Quantum Computing Matthew Dietrich, Ryan Bowler, Gary Howell, Adam Kleczewski, Nathan Kurz, Viki Mirgon,

    E-print Network

    Blinov, Boris

    Barium Ions for Quantum Computing Matthew Dietrich, Ryan Bowler, Gary Howell, Adam Kleczewski+ make it an excellent qubit candidate. Here we report trapping 138Ba+, an even isotope of barium production, using the S1/2 to P3/2 transition. Barium as a Qubit The two hyperfine levels of the 137Ba

  8. Diverse patterns of ocean export productivity change across the Cretaceous-7 Paleogene boundary: new insights from biogenic barium8

    E-print Network

    Paleogene boundary: new insights from biogenic barium8 9 10 11 12 Pincelli M. Hull1,2 and Richard D. Norris1 productivity patterns using new and compiled measurements of biogenic barium. Unlike a53 previous synthesis, we barium and other proxies in the central57 Pacific and some upwelling or neritic Atlantic sites indicate

  9. Self-biased planar millimeter wave notch filters based on magnetostatic wave excitation in barium hexagonal ferrite thin films

    E-print Network

    Self-biased planar millimeter wave notch filters based on magnetostatic wave excitation in barium; accepted 29 September 2010; published online 25 October 2010 The use of M-type barium hexagonal ferrite Ba-type barium hexagonal ferrite BaFe12O19 BaM thin films, as a replacement for those cubic garnets.4 Hexagonal

  10. Crossed-Beam Reactions of Barium with Hydrogen Halides Measurement of Internal State Distributions by Laser-Induced Fluorescence

    E-print Network

    Crossed-Beam Reactions of Barium with Hydrogen Halides Measurement of Internal State Distributions is presented and applied to the reactions of barium with the hydrogen halides. It is found that most-inducedfluorescenceas a molecular beam detector and apply it to the reactions of barium atoms with hydrogen halides, Reactions (1

  11. The effect of Pt interlayers on the magnetic and structural properties of perpendicularly oriented barium ferrite media

    E-print Network

    Laughlin, David E.

    barium ferrite media Zailong Zhuang,a) Maithri Rao, David E. Laughlin, and Mark H. Kryder Data Storage Systems Center, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213 Perpendicular barium ferrite Ba-axis orientation for thicker films, Pt interlayers were added into the barium ferrite films. This article thus

  12. AlGaN/GaN metal-oxide-semiconductor heterostructure field-effect transistors using barium strontium titanate

    E-print Network

    York, Robert A.

    AlGaN/GaN metal-oxide-semiconductor heterostructure field-effect transistors using barium strontium-effect transistors have been formed by incorporating barium strontium titanate (BST) deposited by rf magnetron in increased leakage. Due to its large dielectric constant, barium strontium ti- tanate [Ba1-xSrxTiO3, (BST

  13. IEEE TRANSACTIONS ON MAGNETICS, VOL. 37, NO. 4, JULY 2001 2589 Barium and Strontium Ferrite Perpendicular Thin

    E-print Network

    Laughlin, David E.

    IEEE TRANSACTIONS ON MAGNETICS, VOL. 37, NO. 4, JULY 2001 2589 Barium and Strontium FerriteAlSi) as the soft magnetic underlayer for hexagonal barium ferrite (BaM) and strontium ferrite (SrM) was studied--Barium ferrite, multi-layer, sendust, soft under- layer, strontium ferrite, textured growth. I. INTRODUCTION M

  14. Impacts on Global Agriculture of Stratospheric Sulfate Injection

    NASA Astrophysics Data System (ADS)

    Robock, A.; Xia, L.

    2014-12-01

    Impacts on global food supply are one of the most important concerns in the discussion of stratospheric sulfate geoengineering. Stratospheric sulfate injection could reduce surface temperature, precipitation, and insolation, which could affect agricultural production. We use output from climate model simulations using the two most "realistic" scenarios from the Geoengineering Model Intercomparison Project, G3 and G4. G3 posits balancing the increasing radiative forcing from the RCP4.5 business-as-usual scenario with stratospheric sulfate aerosols from 2020 through 2070. The G4 scenario also uses RCP4.5, but models simulate the stratospheric injection of 5 Tg SO2 per year from 2020 to 2070. In total, there are three modeling groups which have completed G3 and four for G4. We use two crop models, the global gridded Decision Support System for Agrotechnology Transfer (gDSSAT) crop model and the crop model in the NCAR Community Land Model (CLM-crop), to predict global maize yield changes. Without changing agricultural technology, we find that compared to the reference run forced by the RCP4.5 scenario, maize yields could increase in both G3 and G4 due to both the cooling effect of stratospheric sulfate injection and the CO2 fertilization effect, with the cooling effect contributing more to the increased productivity. However, the maize yield changes are not much larger than natural variability under G3, since the temperature reduction is smaller in G3 than in G4. Both crop models show similar results.

  15. Effect of topography on sulfate redistribution in Cumulonimbus cloud development.

    PubMed

    Vujovi?, Dragana; Vu?kovi?, Vladan; Curi?, Mla?en

    2014-03-01

    An aqueous chemical module is created and included into a complex three-dimensional atmospheric cloud-resolving mesoscale model. In the chemical module, oxidation of S(IV) by ozone and hydrogen peroxide in cloud-water and rainwater, as important process of the sulfate production is included. To examine the impact of topography on the sulfate redistribution in a clean and a polluted environment, the complex topography of Serbia is included in the model. Numerical simulations of an isolated summer Cumulonimbus cloud shows that thunderstorms generate very strong vertical sulfate redistribution from the planetary boundary layer to the upper troposphere. This redistribution is sensitive to cloud dynamics, while cloud microphysics and precipitation determine wet removal of the chemical species. In simulations with realistic topography, the chemical species are transported over larger distances close to the surface, while in the upper atmosphere, there is no difference compared to the simulations without topography. The sensitivity tests of cloud chemistry to the physical processes are made. Omission of nucleation and impact scavenging of aerosols in the model simulations shows that 75.8 and 62.5 % of total sulfur mass deposited in the base experiment for the clean and the polluted environment, respectively, is the result of other processes. Exclusion of oxidation accounted for 19.2 and 37.7 % of total sulfur deposited for clean and polluted environment. Ignoring the ice phase almost not change mass of deposited sulfur: there is an increase of 2.9 and 1.5 % for clean and polluted atmosphere, respectively. Real topography conditions affect the sulfate redistribution in the sense of greater possibilities of transport. Numerical simulations without real topography give an artificial increase of deposited sulfur mass of about 25-30 %. PMID:24243093

  16. Centrifugal Jet Spinning for Highly Efficient and Large-scale Fabrication of Barium Titanate Nanofibers

    PubMed Central

    Ren, Liyun; Kotha, Shiva P.

    2014-01-01

    The centrifugal jet spinning (CJS) method has been developed to enable large-scale synthesis of barium titanate nanofibers. Barium titanate nanofibers with fiber diameters down to 50 nm and grain sizes around 25 nm were prepared with CJS by spinning a sol-gel solution of barium titanate and poly(vinylpyrrolidone) with subsequent heat treatment at 850 °C. XRD and FTIR analysis demonstrated high purity and tetragonal perovskite structured barium titanate nanofibers. SEM and TEM images confirm the continuous high aspect ratio structure of barium titanate nanofibers after heat treatment. It is demonstrated that the CJS technique offers a highly efficient method for large-scale fabrication of ceramic nanofibers at production rates of up to 0.3 gram/minute. PMID:24563566

  17. Fabrication of barium/strontium carbonate coated amorphous carbon nanotubes as an improved field emitter

    NASA Astrophysics Data System (ADS)

    Maity, S.; Jha, A.; Das, N. S.; Chattopadhyay, K. K.

    2013-02-01

    Amorphous carbon nanotubes (aCNTs) were synthesized by a chemical reaction between ferrocene and ammonium chloride at a temperature ˜250 ?C in an air furnace. As-synthesized aCNTs were coated with the barium/strontium carbonate through a simple chemical process. The coating of barium/strontium carbonate was confirmed by a high resolution transmission electron microscopy, X-ray diffraction, and Fourier transformed infrared spectroscopy. Morphology of the as-prepared samples was studied by field emission scanning electron microscopy. Thermal gravimetric analysis showed that barium/strontium carbonate coated aCNTs are more stable than the pristine aCNTs. As-prepared barium/strontium carbonate coated aCNTs showed significantly improved field emission properties with a turn-on field as low as 2.5 V/?m. The variation of field emission characteristics of the barium/strontium carbonate coated aCNTs with interelectrode distances was also studied.

  18. Radium and barium in the Amazon River system

    SciTech Connect

    Moore, W.S.; Edmond, J.M.

    1984-03-20

    Data for /sup 226/Ra and /sup 228/Ra in the Amazon River system show that the activity of each radium isotope is strongly correlated with barium concentrations. Two trends are apparent, one for rivers which drain shield areas and another for all other rivers. These data suggest that there has been extensive fractionation of U, Th, and Ba during weathering in the Amazon basin. The /sup 226/Ra data fit a flux model for the major ions indicating that /sup 226/Ra behaves conservatively along the main channel of the Amazon River.

  19. Strain engineered barium strontium titanate for tunable thin film resonators

    NASA Astrophysics Data System (ADS)

    Khassaf, H.; Khakpash, N.; Sun, F.; Sbrockey, N. M.; Tompa, G. S.; Kalkur, T. S.; Alpay, S. P.

    2014-05-01

    Piezoelectric properties of epitaxial (001) barium strontium titanate (BST) films are computed as functions of composition, misfit strain, and temperature using a non-linear thermodynamic model. Results show that through adjusting in-plane strains, a highly adaptive rhombohedral ferroelectric phase can be stabilized at room temperature with outstanding piezoelectric response exceeding those of lead based piezoceramics. Furthermore, by adjusting the composition and the in-plane misfit, an electrically tunable piezoelectric response can be obtained in the paraelectric state. These findings indicate that strain engineered BST films can be utilized in the development of electrically tunable and switchable surface and bulk acoustic wave resonators.

  20. Aspiration of barium-impregnated polyethylene spheres by a dog.

    PubMed

    Greci, V; Bissett, S A; Copple, C N; Hawkins, E C

    2010-05-01

    This case report describes an 11-year-old Belgian Malinois dog with acute onset of cough caused by aspiration of barium-impregnated polyethylene spheres (BIPS) and pneumonia following an episode of suspected gastric dilation. Although bronchoscopic retrieval of the BIPS was largely unsuccessful, the dog recovered uneventfully, with most of the BIPS being coughed out and swallowed over a 1-month period. Aspiration of BIPS should be considered a potential complication of their administration. Furthermore, endoscopic removal of aspirated BIPS is challenging and may not be indicated because of their inert nature and possible self-clearance. PMID:20529021

  1. Two barium plasma injections into the northern magnetospheric cleft

    NASA Technical Reports Server (NTRS)

    Jeffries, R. A.; Roach, W. H.; Hones, E. W., Jr.; Wescott, E. M.; Stenbaek-Nielsen, H. C.; Davis, T. N.; Winningham, J. D.

    1975-01-01

    Two rocket experiments, performed in January 1975, investigated convection of plasma formed by solar photoionization of barium injected into the northern magnetospheric cleft at 13 km/s upward and parallel to the local geomagnetic field. Plasma convection was demonstrated from the cleft's poleward region, directly into and across the polar cap, and possibly into the convection system of the nightside auroral electrojet; plasma injected centrally within the cleft under quiet magnetic conditions remained in the cleft convection system for at least 22 min and revealed a highly structured E-field over about 600 km of longitudinal extent. Cleft location agreed with that predicted by ionosondes.

  2. A barium-rich binary central star in Abell 70

    NASA Astrophysics Data System (ADS)

    Boffin, Henri M. J.; Miszalski, Brent; Frew, David J.; Acker, Agnes; Köppen, Joachim; Moffat, Anthony F. J.; Parker, Quentin A.

    2012-08-01

    We have found the central star of Abell 70 (PN G038.1-25.4, hereafter A 70) to be a binary consisting of a G8 IV-V secondary and a hot white dwarf. The secondary shows enhanced Ba II and Sr II features, firmly classifying it as a barium star. The nebula is found to have Type-I chemical abundances with helium and nitrogen enrichment, which combined with future abundance studies of the central star, will establish A 70 as a unique laboratory for studying s-process AGB nucleosynthesis.

  3. Enhanced flexoelectricity through residual ferroelectricity in barium strontium titanate

    SciTech Connect

    Garten, Lauren M. Trolier-McKinstry, Susan

    2015-03-07

    Residual ferroelectricity is observed in barium strontium titanate ceramics over 30?°C above the global phase transition temperature, in the same temperature range in which anomalously large flexoelectric coefficients are reported. The application of a strain gradient leads to strain gradient-induced poling or flexoelectric poling. This was observed by the development of a remanent polarization in flexoelectric measurements, an induced d{sub 33} piezoelectric response even after the strain gradient was removed, and the production of an internal bias of 9?kV m{sup ?1}. It is concluded that residual ferroelectric response considerably enhances the observed flexoelectric response.

  4. Dielectric behavior of barium modified strontium bismuth titanate ceramic

    SciTech Connect

    Nayak, P.; Badapanda, T.; Anwar, S.; Panigrahi, S.

    2014-04-24

    Barium Modified Strontium Bismuth Titanate(SBT) ceramic with general formula Sr1?xBaxBi4Ti4O15 is prepared by solid state reaction route. The structural analysis of the ceramics was done by X-ray diffraction technique. The X-ray patterns show that all the compositions are of single phase with orthorhombic structure. The temperature dependent dielectric behavior shows that the transition temperature decreases with Ba content but the maximum dielectric constant increases. The decreases of the transition with increase in Ba{sup 2+} ion, may be due to the decrease of orthorhombicity by the incorporation of Ba{sup 2+} ion in SBT lattice.

  5. Strain engineered barium strontium titanate for tunable thin film resonators

    SciTech Connect

    Khassaf, H.; Khakpash, N.; Sun, F.; Sbrockey, N. M.; Tompa, G. S.; Kalkur, T. S.; Alpay, S. P.

    2014-05-19

    Piezoelectric properties of epitaxial (001) barium strontium titanate (BST) films are computed as functions of composition, misfit strain, and temperature using a non-linear thermodynamic model. Results show that through adjusting in-plane strains, a highly adaptive rhombohedral ferroelectric phase can be stabilized at room temperature with outstanding piezoelectric response exceeding those of lead based piezoceramics. Furthermore, by adjusting the composition and the in-plane misfit, an electrically tunable piezoelectric response can be obtained in the paraelectric state. These findings indicate that strain engineered BST films can be utilized in the development of electrically tunable and switchable surface and bulk acoustic wave resonators.

  6. as the Strengthening Precipitates

    NASA Astrophysics Data System (ADS)

    Lu, Qi; Xu, Wei; van der Zwaag, Sybrand

    2014-12-01

    Generally, Laves phase and M23C6 are regarded as undesirable phases in creep-resistant steels due to their very high-coarsening rates and the resulting depletion of beneficial alloying elements from the matrix. In this study, a computational alloy design approach is presented to develop martensitic steels strengthened by Laves phase and/or M23C6, for which the coarsening rates are tailored such that they are at least one order of magnitude lower than those in existing alloys. Their volume fractions are optimized by tuning the chemical composition in parallel. The composition domain covering 10 alloying elements at realistic levels is searched by a genetic algorithm to explore the full potential of simultaneous maximization of the volume fraction and minimization of the precipitates coarsening rate. The calculations show that Co and W can drastically reduce the coarsening rate of Laves and M23C6 and yield high-volume fractions of precipitates. Mo on the other hand was shown to have a minimal effect on coarsening. The strengthening effects of Laves phase and M23C6 in the newly designed alloys are compared to existing counterparts, showing substantially higher precipitation-strengthening contributions especially after a long service time. New alloys were designed in which both Laves phase and M23C6 precipitates act as strengthening precipitates. Successfully combining MX and M23C6 was found to be impossible.

  7. Endotrophic Calcium, Strontium, and Barium Spores of Bacillus megaterium and Bacillus cereus1

    PubMed Central

    Foerster, Harold F.; Foster, J. W.

    1966-01-01

    Foerster, Harold F. (The University of Texas, Austin), and J. W. Foster. Endotrophic calcium, strontium, and barium spores of Bacillus megaterium and Bacillus cereus. J. Bacteriol. 91:1333–1345. 1966.—Spores were produced by washed vegetative cells suspended in deionized water supplemented with CaCl2, SrCl2, or BaCl2. Normal, refractile spores were produced in each case; a portion of the barium spores lost refractility and darkened. Thin-section electron micrographs revealed no apparent anatomical differences among the three types of spores. Analyses revealed that the different spore types were enriched specifically in the metal to which they were exposed during sporogenesis. The calcium content of the strontium and the barium spores was very small. From binary equimolar mixtures of the metal salts, endotrophic spores accumulated both metals to nearly the same extent. Viability of the barium spores was considerably less than that of the other two types. Strontium and barium spores were heat-resistant; however, calcium was essential for maximal heat resistance. Significant differences existed in the rates of germination; calcium spores germinated fastest, strontium spores were slower, and barium spores were slowest. Calcium-barium and calcium-strontium spores germinated readily. Endotrophic calcium and strontium spores germinated without the prior heat activation essential for growth spores. Chemical germination of the different metal-type spores with n-dodecylamine took place at the same relative rates as physiological germination. Heat-induced release of dipicolinic acid occurred much faster with barium and strontium spores than with calcium spores. The washed “coat fraction” from disrupted spores contained little of the spore calcium but most of the spore barium. The metal in this fraction was released by dilute acid. The demineralized coats reabsorbed calcium and barium at neutral pH. Images PMID:4956334

  8. Tungsten and Barium Transport in the Internal Plasma of Hollow Cathodes

    NASA Technical Reports Server (NTRS)

    Polk, James E.; Mikellides, Ioannis G.; Katz, Ira; Capece, Angela M.

    2008-01-01

    The effect of tungsten erosion, transport and redeposition on the operation of dispenser hollow cathodes was investigated in detailed examinations of the discharge cathode inserts from an 8200 hour and a 30,352 hour ion engine wear test. Erosion and subsequent re-deposition of tungsten in the electron emission zone at the downstream end of the insert reduces the porosity of the tungsten matrix, preventing the flow of barium from the interior. This inhibits the interfacial reactions of the barium-calcium-aluminate impregnant with the tungsten in the pores. A numerical model of barium transport in the internal xenon discharge plasma shows that the barium required to reduce the work function in the emission zone can be supplied from upstream through the gas phase. Barium that flows out of the pores of the tungsten insert is rapidly ionized in the xenon discharge and pushedback to the emitter surface by the electric field and drag from the xenon ion flow. Thisbarium ion flux is sufficient to maintain a barium surface coverage at the downstream endgreater than 0.6, even if local barium production at that point is inhibited by tungsten deposits. The model also shows that the neutral barium pressure exceeds the equilibrium vapor pressure of the impregnant decomposition reaction over much of the insert length,so the reactions are suppressed. Only a small region upstream of the zone blocked by tungsten deposits is active and supplies the required barium. These results indicate that hollowcathode failure models based on barium depletion rates in vacuum dispenser cathodes are very conservative.

  9. Linking Microbial Ecology to Geochemistry in Sulfate Reducing Systems

    NASA Astrophysics Data System (ADS)

    Drennan, D. M.; Lee, I.; Landkamer, L.; Almstrand, R.; Figueroa, L. A.; Sharp, J. H.

    2013-12-01

    Sulfate reducing bioreactors (SRBRs) can serve as passive treatment systems for mining influenced waters (MIW). An enhanced understanding of the biogeochemistry and efficacy of SRBRs can be achieved by combining molecular biological and geochemical techniques in both field and column settings. To this end, a spatial and temporal sequence of eight pilot-scale columns were analyzed employing a multidisciplinary approach using ICP-AES, next-generation sequencing, and SEM-EDX to explore the effects of variable substrate on community structure and performance (measured by Zn removal). All pilot scale reactors contained 30% limestone by mass, 7 of the 8 had variable amounts of woodchips, sawdust, and alfalfa hay, and an 8th column where the only carbon source was walnut shells. High throughput sequencing of DNA extracted from liquid in pilot-scale columns reveals, similarly to an analogous field system in Arizona, a dominance of Proteobacteria. However, after the first pore volume, performance differences between substrate permutations emerged, where columns containing exclusively walnut shells or sawdust exhibited a more effective startup and metal removal than did columns containing exclusively woodchips or alfalfa hay. SEM-EDX analysis revealed the initial formation of gypsum (CaSO4) precipitates regardless of substrate. Zn was observed in the presence of Ca, S, and O in some column samples, suggesting there was co-precipitation of Zn and CaSO4. This is congruent with micro-XAS analysis of field data suggesting iron sulfides were co-precipitating with gypsum. A SEM-EDX analysis from a subsequent sampling event (8 months into operation) indicated that precipitation may be shifting to ZnS and ZnCO3. Biplots employing Canonical Correspondence Analysis (CCA) describe how diversity scales with performance and substrate selection, and how community shifts may result in differential performance and precipitation in response to selective pressure of bioreactor material on community composition. CCA of Shannon diversity data after one pore volume revealed that zinc removal, walnut shell content, and abundance of delta-Proteobacteria (sulfate reducing organisms) were all corresponding elements. However, after several pore volumes, the walnut shell column was no longer removing Zn as effectively, and community shifts were observed throughout the columns. Analysis of field and laboratory scale microbiological and geochemical shifts, in parallel, gives insight into key biogeochemical variables linked to the performance of passive remediation systems used for the treatment of contaminated MIW, while also providing further insight into metal immobilization at the microbe-mineral interface.

  10. Functionalized synchrotron in-line phase-contrast computed tomography: a novel approach for simultaneous quantification of structural alterations and localization of barium-labelled alveolar macrophages within mouse lung samples

    PubMed Central

    Dullin, Christian; dal Monego, Simeone; Larsson, Emanuel; Mohammadi, Sara; Krenkel, Martin; Garrovo, Chiara; Biffi, Stefania; Lorenzon, Andrea; Markus, Andrea; Napp, Joanna; Salditt, Tim; Accardo, Agostino; Alves, Frauke; Tromba, Giuliana

    2015-01-01

    Functionalized computed tomography (CT) in combination with labelled cells is virtually non-existent due to the limited sensitivity of X-ray-absorption-based imaging, but would be highly desirable to realise cell tracking studies in entire organisms. In this study we applied in-line free propagation X-ray phase-contrast CT (XPCT) in an allergic asthma mouse model to assess structural changes as well as the biodistribution of barium-labelled macrophages in lung tissue. Alveolar macrophages that were barium-sulfate-loaded and fluorescent-labelled were instilled intratracheally into asthmatic and control mice. Mice were sacrificed after 24?h, lungs were kept in situ, inflated with air and scanned utilizing XPCT at the SYRMEP beamline (Elettra Synchrotron Light Source, Italy). Single-distance phase retrieval was used to generate data sets with ten times greater contrast-to-noise ratio than absorption-based CT (in our setup), thus allowing to depict and quantify structural hallmarks of asthmatic lungs such as reduced air volume, obstruction of airways and increased soft-tissue content. Furthermore, we found a higher concentration as well as a specific accumulation of the barium-labelled macrophages in asthmatic lung tissue. It is believe that XPCT will be beneficial in preclinical asthma research for both the assessment of therapeutic response as well as the analysis of the role of the recruitment of macrophages to inflammatory sites. PMID:25537601

  11. Functionalized synchrotron in-line phase-contrast computed tomography: a novel approach for simultaneous quantification of structural alterations and localization of barium-labelled alveolar macrophages within mouse lung samples.

    PubMed

    Dullin, Christian; dal Monego, Simeone; Larsson, Emanuel; Mohammadi, Sara; Krenkel, Martin; Garrovo, Chiara; Biffi, Stefania; Lorenzon, Andrea; Markus, Andrea; Napp, Joanna; Salditt, Tim; Accardo, Agostino; Alves, Frauke; Tromba, Giuliana

    2015-01-01

    Functionalized computed tomography (CT) in combination with labelled cells is virtually non-existent due to the limited sensitivity of X-ray-absorption-based imaging, but would be highly desirable to realise cell tracking studies in entire organisms. In this study we applied in-line free propagation X-ray phase-contrast CT (XPCT) in an allergic asthma mouse model to assess structural changes as well as the biodistribution of barium-labelled macrophages in lung tissue. Alveolar macrophages that were barium-sulfate-loaded and fluorescent-labelled were instilled intratracheally into asthmatic and control mice. Mice were sacrificed after 24 h, lungs were kept in situ, inflated with air and scanned utilizing XPCT at the SYRMEP beamline (Elettra Synchrotron Light Source, Italy). Single-distance phase retrieval was used to generate data sets with ten times greater contrast-to-noise ratio than absorption-based CT (in our setup), thus allowing to depict and quantify structural hallmarks of asthmatic lungs such as reduced air volume, obstruction of airways and increased soft-tissue content. Furthermore, we found a higher concentration as well as a specific accumulation of the barium-labelled macrophages in asthmatic lung tissue. It is believe that XPCT will be beneficial in preclinical asthma research for both the assessment of therapeutic response as well as the analysis of the role of the recruitment of macrophages to inflammatory sites. PMID:25537601

  12. Extracellular iron-sulfur precipitates from growth of Desulfovibrio desulfuricans

    SciTech Connect

    Antonio, M. R.; Tischler, M. L.; Witzcak, D.

    1999-12-20

    The authors have examined extracellular iron-bearing precipitates resulting from the growth of Desulfovibrio desulfuricans in a basal medium with lactate as the carbon source and ferrous sulfate. Black precipitates were obtained when D. desulfuricans was grown with an excess of FeSO{sub 4}. When D. desulfuricans was grown under conditions with low amounts of FeSO{sub 4}, brown precipitates were obtained. The precipitates were characterized by iron K-edge XAFS (X-ray absorption fine structure), {sup 57}Fe Moessbauer-effect spectroscopy, and powder X-ray diffraction. Both were noncrystalline and nonmagnetic (at room temperature) solids containing high-spin Fe(III). The spectroscopic data for the black precipitates indicate the formation of an iron-sulfur phase with 6 nearest S neighbors about Fe at an average distance of 2.24(1) {angstrom}, whereas the brown precipitates are an iron-oxygen-sulfur phase with 6 nearest O neighbors about Fe at an average distance of 1.95(1) {angstrom}.

  13. Interaction of Sodium Dodecyl Sulfate with watermelon chromoplasts and examination of the organization of lycopene within the chromoplasts

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The properties of plant-derived precipitates of watermelon lycopene were examined in aqueous sodium dodecyl sulfate (SDS) as part of an ongoing effort to develop simpler, more economical ways to quantify carotenoids in melon fruit. Levels of SDS >0.2% were found to increase the water solubility of ...

  14. CORRECTING RADM'S SULFATE UNDERPREDICTION: DISCOVERY AND CORRECTION OF MODEL ERRORS AND TESTING THE CORRECTIONS THROUGH COMPARISONS AGAINST FIELD DATA

    EPA Science Inventory

    A serious underprediction of ambient sulfate (SO2-4) by two comprehensive, Eulerian models of acid deposition, the Regional Acid Deposition Model (RADM) and the Acid Deposition and Oxidant Model (ADOM), was found in the National Acid Precipitation Assessment Program phase of the ...

  15. Inhibition of synthesis of heparan sulfate by selenate: Possible dependence on sulfation for chain polymerization

    SciTech Connect

    Dietrich, C.P.; Nader, H.B. ); Buonassisi, V.; Colburn, P. )

    1988-01-01

    Selenate, a sulfation inhibitor, blocks the synthesis of heparan sulfate and chondroitin sulfate by cultured endothelial cells. In contrast, selenate does not affect the production of hyaluronic acid, a nonsulfated glycosaminoglycan. No differences in molecular weight, ({sup 3}H)glucosamine/({sup 35}S)sulfuric acid ratios, or disaccharide composition were observed when the heparan sulfate synthesized by selenate-treated cells was compared with that of control cells. The absence of undersulfated chains in preparations from cultures exposed to selenate supports the concept that, in the intact cell, the polymerization of heparan sulfate might be dependent on the sulfation of the saccharide units added to the growing glycosaminoglycan chain.

  16. Water balance and magnesium control in electrolytic zinc plants using the E.Z. selective zinc precipitation process

    NASA Astrophysics Data System (ADS)

    Matthew, I. G.; Newman, O. M. G.; Palmer, D. J.

    1980-03-01

    There is an increasing tendency for modern electrolytic zinc plants to experience water balance and magnesium control problems because of the simultaneous need to maximize zinc recovery and produce environmentally acceptable leach residues and precipitates. The Selective Zinc Precipitation process developed by the Electrolytic Zinc Company of Australasia involves the precipitation of basic zinc sulfate using limestone. Water balance and magnesium control may be achieved by either discarding the process filtrate, or by using it to wash precipitates in a closed circuit operation. The process filter cake is used as a neutralizing agent in the zinc plant. The process can be operated over a wide range of temperatures and calcined zinc concentrate may be preferred to limestone as a zinc precipitant to minimize the discard of sulfate. This paper is particularly concerned with a quantitative assessment of various modes of integrating the process into modern electrolytic zinc plants.

  17. Characterizing the early stages of electrochemical phase formation of lead sulfate films

    SciTech Connect

    Murugan, K.; Vanmathi, G.; Rangarajan, S.K.

    1995-06-01

    A semiquantitative evaluation of lead sulfate film formation on lead in sulfuric acid solution was done by current-time transient studies. The effects of acid concentration, potential, and expander are explored. Crucial parameters of film formation and passivation are identified which could be used for selection of an electrolyte concentration as well as screening of expanders and their concentration for lead-acid battery negative plate operation.The mechanism of formation of Pb{sup 2+} (PbSO{sub 4}) from lead was confirmed to involve two, one-electron, steps; the second electron transfer being the rate-determining step. Expanders do not affect the Tafel slope but favor the mechanism through dissolution-precipitation mode. The kinetics of lead-sulfate formation do not follow any of the reported/known models. The dissolution-precipitation model coupled with nucleation and a growth model/theory is indicated.

  18. Macrophage secretory products selectively stimulate dermatan sulfate proteoglycan production in cultured arterial smooth muscle cells

    SciTech Connect

    Edwards, I.J.; Wagner, W.D.; Owens, R.T. )

    1990-03-01

    Arterial dermatan sulfate proteoglycan has been shown to increase with atherosclerosis progression, but factors responsible for this increase are unknown. To test the hypothesis that smooth muscle cell proteoglycan synthesis may be modified by macrophage products, pigeon arterial smooth muscle cells were exposed to the media of either cholesteryl ester-loaded pigeon peritoneal macrophages or a macrophage cell line P388D1. Proteoglycans radiolabeled with (35S)sulfate and (3H)serine were isolated from culture media and smooth muscle cells and purified following precipitation with 1-hexadecylpyridinium chloride and chromatography. Increasing concentrations of macrophage-conditioned media were associated with a dose-response increase in (35S)sulfate incorporation into secreted proteoglycans, but there was no change in cell-associated proteoglycans. Incorporation of (3H)serine into total proteoglycan core proteins was not significantly different (5.2 X 10(5) dpm and 5.5 X 10(5) disintegrations per minute (dpm) in control and conditioned media-treated cultures, respectively), but selective effects were observed on individual proteoglycan types. Twofold increases in dermatan sulfate proteoglycan and limited degradation of chondroitin sulfate proteoglycan were apparent based on core proteins separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). Immunoinhibition studies indicated that interleukin-1 was involved in the modulation of proteoglycan synthesis by macrophage-conditioned media. These data provide support for the role of macrophages in alteration of the matrix proteoglycans synthesized by smooth muscle cells and provide a mechanism to account for the reported increased dermatan sulfate/chondroitin sulfate ratios in the developing atherosclerotic lesion.

  19. Barium titanate core – gold shell nanoparticles for hyperthermia treatments

    PubMed Central

    FarrokhTakin, Elmira; Ciofani, Gianni; Puleo, Gian Luigi; de Vito, Giuseppe; Filippeschi, Carlo; Mazzolai, Barbara; Piazza, Vincenzo; Mattoli, Virgilio

    2013-01-01

    The development of new tools and devices to aid in treating cancer is a hot topic in biomedical research. The practice of using heat (hyperthermia) to treat cancerous lesions has a long history dating back to ancient Greece. With deeper knowledge of the factors that cause cancer and the transmissive window of cells and tissues in the near-infrared region of the electromagnetic spectrum, hyperthermia applications have been able to incorporate the use of lasers. Photothermal therapy has been introduced as a selective and noninvasive treatment for cancer, in which exogenous photothermal agents are exploited to achieve the selective destruction of cancer cells. In this manuscript, we propose applications of barium titanate core–gold shell nanoparticles for hyperthermia treatment against cancer cells. We explored the effect of increasing concentrations of these nanoshells (0–100 ?g/mL) on human neuroblastoma SH-SY5Y cells, testing the internalization and intrinsic toxicity and validating the hyperthermic functionality of the particles through near infrared (NIR) laser-induced thermoablation experiments. No significant changes were observed in cell viability up to nanoparticle concentrations of 50 ?g/mL. Experiments upon stimulation with an NIR laser revealed the ability of the nanoshells to destroy human neuroblastoma cells. On the basis of these findings, barium titanate core–gold shell nanoparticles resulted in being suitable for hyperthermia treatment, and our results represent a promising first step for subsequent investigations on their applicability in clinical practice. PMID:23847415

  20. Plasma waves associated with the first AMPTE magnetotail barium release

    NASA Technical Reports Server (NTRS)

    Gurnett, D. A.; Anderson, R. R.; Bernhardt, P. A.; Luehr, H.; Haerendel, G.

    1986-01-01

    Plasma waves observed during the March 21, 1985, AMPTE magnetotail barium release are described. Electron plasma oscillations provided local measurements of the plasma density during both the expansion and decay phases. Immediately after the explosion, the electron density reached a peak of about 400,000/cu cm, and then started decreasing approximately as t to the -2.4 as the cloud expanded. About 6 minutes after the explosion, the electron density suddenly began to increase, reached a secondary peak of about 240/cu cm, and then slowly decayed down to the preevent level over a period of about 15 minutes. The density increase is believed to be caused by the collapse of the ion cloud into the diamagnetic cavity created by the initial expansion. The plasma wave intensities observed during the entire event were quite low. In the diamagnetic cavity, electrostatic emissions were observed near the barium ion plasma frequency, and in another band at lower frequencies. A broadband burst of electrostatic noise was also observed at the boundary of the diamagnetic cavity. Except for electron plasma oscillations, no significant wave activity was observed outside of the diamagnetic cavity.

  1. Results of magnetospheric barium ion cloud experiment of 1971

    NASA Technical Reports Server (NTRS)

    Adamson, D.; Fricke, C. L.; Long, S. A. T.

    1975-01-01

    The barium ion cloud experiment involved the release of about 2 kg of barium at an altitude of 31 482 km, a latitude of 6.926 N., and a longitude of 74.395 W. Significant erosion of plasma from the main ion core occurred during the initial phase of the ion cloud expansion. From the motion of the outermost striational filaments, the electric field components were determined to be 0.19 mV/m in the westerly direction and 0.68 mV/m in the inward direction. The differences between these components and those measured from balloons flown in the proximity of the extremity of the field line through the release point implied the existence of potential gradients along the magnetic field lines. The deceleration of the main core was greater than theoretically predicted. This was attributed to the formation of a polarization wake, resulting in an increase of the area of interaction and resistive dissipation at ionospheric levels. The actual orientation of the magnetic field line through the release point differed by about 10.5 deg from that predicted by magnetic field models that did not include the effect of ring current.

  2. Ruthenium and hafnium abundances in giant and dwarf barium stars

    E-print Network

    Allen, D M

    2007-01-01

    We present abundances for Ru and Hf, compare them to abundances of other heavy elements, and discuss the problems found in determining Ru and Hf abundances with laboratory gf-values in the spectra of barium stars. We determined Ru and Hf abundances in a sample of giant and dwarf barium stars, by the spectral synthesis of two RuI (4080.574A and 4757.856A) and two HfII (4080.437A and 4093.155A) transitions. The stellar spectra were observed with FEROS/ESO, and the stellar atmospheric parameters lie in the range 4300 < Teff/K < 6500, -1.2 < [Fe/H] <= 0 and 1.4 <= log g < 4.6. The HfII 4080A and the RuI 4758A observed transitions result in a unreasonably high solar abundance, given certain known uncertainties, when fitted with laboratory gf-values. For these two transitions we determined empirical gf-values by fitting the observed line profiles of the spectra of the Sun and Arcturus. For the sample stars, this procedure resulted in a good agreement of Ru and Hf abundances given by the two availa...

  3. Study examines sulfate-reducing bacteria activity

    SciTech Connect

    McElhiney, J.E.; Hardy, J.A.; Rizk, T.Y.; Stott, J.F.D.; Eden, R.D.

    1996-12-09

    Low-sulfate seawater injection can reduce the potential of an oil reservoir turning sour because of sulfate-reducing bacteria. Sulfate-reducing bacteria (SRB) convert sulfate ions in seawater used in waterflooding into sulfide with the concomitant oxidation of a carbon source. A recent study at Capcis investigated the efficiency of SRB under various conditions of sulfate limitation. This study was conducted in a flowing bioreactor at 2,000 psia with different temperature zones (mesophilic 35 C and thermophilic 60--80 C). The study mixed microfloral populations derived from real North Sea-produced fluids, and included an active population of marine methanogenic bacteria present to provide competition for the available carbon sources. In general, results showed that SRB continue to convert sulfate to sulfide in stoichiometric quantities without regard to absolute concentrations. The paper discusses the results and recommends nanofiltration of seawater for ``sweet`` reservoirs.

  4. Sulfate reduction in freshwater wetland soils and the effects of sulfate and substrate loading

    SciTech Connect

    Feng, J.; Hsieh, Y.P.

    1998-07-01

    Elevated sulfate and organic C loadings in freshwater wetlands could stimulate dissimilatory sulfate reduction that oxidizes organic C, produces hydrogen sulfide and alkalinity, and sequesters trace metals. The authors determined the extent of sulfate reduction in two freshwater wetland soils, that is black gum (Nyssa biflona) swamp soils and titi (Cliftonia monophylla) swamp soils, in northern Florida. They also investigated the potential of sulfate reduction in the wetland soils by adding sulfate, organic substrate, and lime. Sulfate reduction was found to be an active process in both swamp soils without any amendment, where the pore water pH was as low as 3.6 and sulfate concentration was as low as 5 mg L{sup {minus}1}. Without amendment, 11 to 14% of organic C was oxidized through sulfate reduction in the swamp soils. Sulfate loading, liming, and substrate addition significantly increased sulfate reduction in the black gum swamp soil, but none of those treatments increase sulfate reduction in the titi swamp soil. The limiting factor for sulfate reduction in the titi swamp soil were likely texture and soil aggregate related properties. The results suggested that wastewater loading may increase sulfate reduction in some freshwater wetlands such as the black swamps while it has no stimulating effect on other wetlands such as the titi swamps.

  5. Liquid-Phase Processing of Barium Titanate Thin Films

    NASA Astrophysics Data System (ADS)

    Harris, David Thomas

    Processing of thin films introduces strict limits on the thermal budget due to substrate stability and thermal expansion mismatch stresses. Barium titanate serves as a model system for the difficulty in producing high quality thin films because of sensitivity to stress, scale, and crystal quality. Thermal budget restriction leads to reduced crystal quality, density, and grain growth, depressing ferroelectric and nonlinear dielectric properties. Processing of barium titanate is typically performed at temperatures hundreds of degrees above compatibility with metalized substrates. In particular integration with silicon and other low thermal expansion substrates is desirable for reductions in costs and wider availability of technologies. In bulk metal and ceramic systems, sintering behavior has been encouraged by the addition of a liquid forming second phase, improving kinetics and promoting densification and grain growth at lower temperatures. This approach is also widespread in the multilayer ceramic capacitor industry. However only limited exploration of flux processing with refractory thin films has been performed despite offering improved dielectric properties for barium titanate films at lower temperatures. This dissertation explores physical vapor deposition of barium titanate thin films with addition of liquid forming fluxes. Flux systems studied include BaO-B2O3, Bi2O3-BaB2O 4, BaO-V2O5, CuO-BaO-B2O3, and BaO-B2O3 modified by Al, Si, V, and Li. Additions of BaO-B2O3 leads to densification and an increase in average grain size from 50 nm to over 300 nm after annealing at 900 °C. The ability to tune permittivity of the material improved from 20% to 70%. Development of high quality films enables engineering of ferroelectric phase stability using residual thermal expansion mismatch in polycrystalline films. The observed shifts to TC match thermodynamic calculations, expected strain from the thermal expansion coefficients, as well as x-ray diffract measurements . Our system exhibits flux-film-substrate interactions that can lead to dramatic changes to the microstructure. This effect is especially pronounced onc -sapphire, with Al diffusion from the substrate leading to formation of an epitaxial BaAl2O4 second phase at the substrate-film interface. The formation of this second phase in the presence of a liquid phase seeds {111} twins that drive abnormal grain growth. The orientation of the sapphire substrate determines the BaAl2O 4 morphology, enabling control the abnormal grain growth behavior. CuO additions leads to significant grain growth at 900 °C, with average grain size approaching 500 nm. The orthorhombic-tetragonal phase transition is clearly observable in temperature dependent measurements and both linear and nonlinear dielectric properties are improved. All films containing CuO are susceptible to aging. A number of other systems were investigated for efficacy at temperatures below 900 °C. Pulsed laser deposition was used to study flux + BaTiO 3 targets, layered flux films, and in situ liquids. RF-magnetron sputtering using a dual-gun approach was used to explore integration on flexible foils with Ba1-xSrxTiO3. Many of these systems were based on the BaO-B2O3 system, which has proven effective in thin films, multilayer ceramic capacitors, and bulk ceramics. Modifiers allow tailoring of the microstructure at 900 °C, however no compositions were found, and no reports exist in the open literature, that provide significant grain growth or densification below 900 °C. Liquid phase fluxes offer a promising path forward for low temperature processing of barium titanate, with the ultimate goal of integration with metalized silicon substrates. This work demonstrates significant improvements to dielectric properties and the necessity of understanding interactions in the film-flux-substrate system.

  6. Integrated Spectroscopic Studies of Hydrous Sulfate Minerals

    NASA Technical Reports Server (NTRS)

    Dyar, M. D.; Lane, M. D.; Bishop, J. L.; OConnor, V.; Cloutis, E.; Hiroi, T.

    2005-01-01

    Sulfate minerals have been identified in Martian meteorites and on Mars using a suite of instruments aboard the MER rovers. These results have confirmed previous groundbased observations and orbital measurements that suggested their presence. The orbiting OMEGA instrument on Mars Express is also finding evidence for sulfate. In order to better interpret remote-sensing data, we present here the results of a coordinated visible/near infrared (VNIR) reflectance, Moussbauer (MB), and thermal emittance study of wellcharacterized hydrous sulfate minerals.

  7. EFFECTS OF ACID PRECIPITATION

    EPA Science Inventory

    Recent reviews of available data indicate that precipitation in a large region of North America is highly acidic when its pH is compared with the expected pH value of 5.65 for pure rain water in equilibrium with CO2. A growing body of evidence suggests that acid rain is responsib...

  8. Testing Precipitation Gage

    USGS Multimedia Gallery

    During August 2013, the Beaver Creek wildfire burned more than 114,000 acres near the south-central Idaho communities of Sun Valley, Ketchum, and Hailey. Partnering with Blaine County, the USGS installed a network of real-time precipitation gages in the burn area. Real-time information from the gage...

  9. Installing Precipitation Gage

    USGS Multimedia Gallery

    During August 2013, the Beaver Creek wildfire burned more than 114,000 acres near the south-central Idaho communities of Sun Valley, Ketchum, and Hailey. Partnering with Blaine County, the USGS installed a network of real-time precipitation gages in the burn area. Real-time information from the gage...

  10. Orogenic propagating precipitation systems

    NASA Astrophysics Data System (ADS)

    Moncrieff, Mitchell; Pritchard, Mike

    2010-05-01

    Organized propagating systems in the lee of mountains make an important contribution to convective precipitation in midlatitudes (e.g., US during the warm season) and in the tropics throughout the year. These systems display a high degree of variability in regard to the thermodynamic state (i.e., temperature and moisture distribution) and kinetic state (i.e., vertical shear) of the atmosphere. However, propagating precipitation systems are absent from climate models and are inadequately represented in global numerical weather prediction (NWP) models, if they are present at all. The reason is simple. Firstly, traditional cumulus parameterizations do not represent interactions between latent heating, rain evaporation and wind-shear which are fundamental to the mesoscale convective dynamics. Secondly, the spatial resolution of climate models is too coarse to permit explicit mesoscale convective organization. This has practical implications for quantitative precipitation prediction and fundamental implications for the Earth's water cycle and its variability. This talk will describe issues regarding the parameterization of organized convection for climate models, its explicit representation by cloud-system resolving models (CRMs, and hybrid representation for high-resolution NWP models. Also described will be new methodologies for representing propagating precipitation systems in climate models: i)superparameterization whereby traditional convective parameterization is replaced by CRMs; ii) hybrid parametric representation of stratiform heating, mesoscale downdrafts, and organized momentum transport associated with propagating systems.

  11. Total Precipitable Water

    SciTech Connect

    2012-01-01

    The simulation was performed on 64K cores of Intrepid, running at 0.25 simulated-years-per-day and taking 25 million core-hours. This is the first simulation using both the CAM5 physics and the highly scalable spectral element dynamical core. The animation of Total Precipitable Water clearly shows hurricanes developing in the Atlantic and Pacific.

  12. The Global Precipitation Mission

    NASA Technical Reports Server (NTRS)

    Braun, Scott; Kummerow, Christian

    2000-01-01

    The Global Precipitation Mission (GPM), expected to begin around 2006, is a follow-up to the Tropical Rainfall Measuring Mission (TRMM). Unlike TRMM, which primarily samples the tropics, GPM will sample both the tropics and mid-latitudes. The primary, or core, satellite will be a single, enhanced TRMM satellite that can quantify the 3-D spatial distributions of precipitation and its associated latent heat release. The core satellite will be complemented by a constellation of very small and inexpensive drones with passive microwave instruments that will sample the rainfall with sufficient frequency to be not only of climate interest, but also have local, short-term impacts by providing global rainfall coverage at approx. 3 h intervals. The data is expected to have substantial impact upon quantitative precipitation estimation/forecasting and data assimilation into global and mesoscale numerical models. Based upon previous studies of rainfall data assimilation, GPM is expected to lead to significant improvements in forecasts of extratropical and tropical cyclones. For example, GPM rainfall data can provide improved initialization of frontal systems over the Pacific and Atlantic Oceans. The purpose of this talk is to provide information about GPM to the USWRP (U.S. Weather Research Program) community and to discuss impacts on quantitative precipitation estimation/forecasting and data assimilation.

  13. A modified sulfate process to lunar oxygen

    NASA Technical Reports Server (NTRS)

    Sullivan, Thomas A.

    1992-01-01

    A modified sulfate process which produces oxygen from iron oxide-bearing minerals in lunar soil is under development. Reaction rates of ilmenite in varying strength sulfuric acid have been determined. Quantitative conversion of ilmenite to ferrous sulfate was observed over a range of temperatures and concentrations. Data has also been developed on the calcination of by-product sulfates. System engineering for overall operability and simplicity has begun, suggesting that a process separating the digestion and sulfate dissolution steps may offer an optimum process.

  14. FORMATION PROCESSES AND CONSEQUENCES OF REACTIVE AND NON-REACTIVE MINERAL PRECIPITATES IN PERMEABLE REACTIVE BARRIERS

    EPA Science Inventory

    Mineral precipitates in zero-valent iron PRBs can be classified by formation processes into three groups: 1) those that result from changes in chemical conditions (i.e., change in pH, e.g., calcite); 2) those that are a consequence of microbial activity (i.e., sulfate reduction, ...

  15. ASSESSING MINE DRAINAGE WATER QUALITY FROM THE COLOR AND SPECTRAL REFLECTANCE OF CHEMICAL PRECIPITATES

    EPA Science Inventory


    The pH and dissolved sulfate concentrations of mine impacted waters were estimated on the basis of the spectral reflectance of resident sediments composed mostly of chemical precipitates. Mine drainage sediments were collected from sites in the Anthracite Region of eastern Pe...

  16. The Evolving Mixture of Barium Isotopes in Milky Way Halo Stars

    NASA Astrophysics Data System (ADS)

    Choudhury, Zareen; Kirby, E. N.; Guhathakurta, P.

    2014-01-01

    Heavy metals in stars form through one of two types of neutron capture processes: the rapid r-process or slower s-process. The fraction of odd and even barium isotopes in stars can indicate which process predominantly contributed to a star’s heavy metals, since odd barium isotopes predominantly form through the r-process and even barium isotopes through the s-process. The “stellar model” predicts that older stars contain comparable amounts of odd and even barium isotopes, while the “classical model” states that they almost exclusively contain odd isotopes. This study investigated these competing models by analyzing high-resolution spectra of twelve Milky Way stars. These spectra were analyzed for the first time in this study. To quantify r- and s-process enrichment, we measured the odd barium isotope fraction in the stars by fitting models to the stars’ spectra. Generating models involved measuring the stars’ Doppler shift, resolution, and barium abundance. To reduce error margins we optimized resolution and barium abundance measurements by enhancing existing techniques through several rounds of revisions. Our results support the stellar model of heavy metal enrichment, and our proposed optimizations will enable future researchers to obtain a deeper understanding of chemical enrichment in the Universe. This research was supported by the Science Internship Program at the University of California Santa Cruz, Lick Observatory, and the National Science Foundation.

  17. Fabrication and characterization of cerium-doped barium titanate inverse opal by sol-gel method

    SciTech Connect

    Jin Yi; Zhu Yihua Yang Xiaoling; Li Chunzhong; Zhou Jinghong

    2007-01-15

    Cerium-doped barium titanate inverted opal was synthesized from barium acetate contained cerous acetate and tetrabutyl titanate in the interstitial spaces of a polystyrene (PS) opal. This procedure involves infiltration of precursors into the interstices of the PS opal template followed by hydrolytic polycondensation of the precursors to amorphous barium titanate and removal of the PS opal by calcination. The morphologies of opal and inverse opal were characterized by scanning electron microscope (SEM). The pores were characterized by mercury intrusion porosimetry (MIP). X-ray photoelectron spectroscopy (XPS) investigation showed the doping structure of cerium, barium and titanium. And powder X-ray diffraction allows one to observe the influence of doping degree on the grain size. The lattice parameters, crystal size and lattice strain were calculated by the Rietveld refinement method. The synthesis of cerium-doped barium titanate inverted opals provides an opportunity to electrically and optically engineer the photonic band structure and the possibility of developing tunable three-dimensional photonic crystal devices. - Graphical abstract: Cerium-doped barium titanate inverted opal was synthesized from barium acetate acid contained cerous acetate and tetrabutyl titanate in the interstitial spaces of a PS opal, which involves infiltration of precursors into the interstices of the PS opal template and removal of the PS opal by calcination.

  18. Semi-synthesis of chondroitin sulfate-E from chondroitin sulfate-A

    PubMed Central

    Cai, Chao; Solakyildirim, Kemal; Yang, Bo; Beaudet, Julie M.; Weyer, Amanda; Linhardt, Robert J.; Zhang, Fuming

    2011-01-01

    Chondroitin sulfate-E (chondroitin-4, 6-disulfate) was prepared from chondroitin sulfate-A (chondroitin-4 - sulfate) by regioselective sulfonation, performed using trimethylamine sulfur trioxide in formamide under argon. The structure of semi-synthetic chondroitin sulfate-E was analyzed by PAGE, 1H NMR, 13C NMR, 2D NMR and disaccharide analysis and compared with natural chondroitin sulfate-E. Both semi-synthetic and natural chondroitin sulfate-E were each biotinylated and immobilized on BIAcore SA biochips and their interactions with fibroblast growth factors displayed very similar binding kinetics and binding affinities. The current semi-synthesis offers an economical approach for the preparation of the rare chondroitin sulfate-E from the readily available chondroitin sulfate-A. PMID:22140285

  19. Fluidized Bed Selective Oxidation-Sulfation Roasting of Nickel Sulfide Concentrate: Part II. Sulfation Roasting

    NASA Astrophysics Data System (ADS)

    Yu, Dawei; Utigard, Torstein A.; Barati, Mansoor

    2014-04-01

    The fluidized bed sulfation roasting process followed by water leaching was investigated as an alternative process to treat nickel sulfide concentrate for nickel production. The effects of several roasting parameters, such as the sulfation gas flow rate, roasting temperature, the addition of Na2SO4, and the roasting time, were studied. 79 pct Ni, 91 pct Cu, and 95 pct Co could be recovered with minimal dissolution of Fe of 4 pct by water leaching after two-stage oxidation-sulfation roasting under optimized conditions. The sulfation roasting mechanism was investigated, showing that the outermost layer of sulfate melt and the porous iron oxide layer create a favorable sulfation environment with high partial pressure of SO3. Sulfation of the sulfide core was accompanied by the conversion of the sulfide from Ni1- x S to Ni7S6 as well as inward diffusion of the sulfation gas.

  20. Characterisation of Ba(OH){sub 2}–Na{sub 2}SO{sub 4}–blast furnace slag cement-like composites for the immobilisation of sulfate bearing nuclear wastes

    SciTech Connect

    Mobasher, Neda; Bernal, Susan A.; Hussain, Oday H.; Apperley, David C.; Kinoshita, Hajime; Provis, John L.

    2014-12-15

    Soluble sulfate ions in nuclear waste can have detrimental effects on cementitious wasteforms and disposal facilities based on Portland cement. As an alternative, Ba(OH){sub 2}–Na{sub 2}SO{sub 4}–blast furnace slag composites are studied for immobilisation of sulfate-bearing nuclear wastes. Calcium aluminosilicate hydrate (C–A–S–H) with some barium substitution is the main binder phase, with barium also present in the low solubility salts BaSO{sub 4} and BaCO{sub 3}, along with Ba-substituted calcium sulfoaluminate hydrates, and a hydrotalcite-type layered double hydroxide. This reaction product assemblage indicates that Ba(OH){sub 2} and Na{sub 2}SO{sub 4} act as alkaline activators and control the reaction of the slag in addition to forming insoluble BaSO{sub 4}, and this restricts sulfate availability for further reaction as long as sufficient Ba(OH){sub 2} is added. An increased content of Ba(OH){sub 2} promotes a higher degree of reaction, and the formation of a highly cross-linked C–A–S–H gel. These Ba(OH){sub 2}–Na{sub 2}SO{sub 4}–blast furnace slag composite binders could be effective in the immobilisation of sulfate-bearing nuclear wastes.

  1. The catalytic effect of bound extracellular polymeric substances excreted by anaerobic microorganisms on Ca-Mg carbonate precipitation: Implications for the "dolomite problem"

    E-print Network

    Johnson, Clark M.

    microorganisms on Ca-Mg carbonate precipitation: Implications for the "dolomite problem" FangFu Zhang1, , hui as the difficulty in synthesizing it under low-temperature conditions in the laboratory, the origin of sedimentary bacteria and sulfate-reducing bacteria on Ca-Mg carbonate precipitation. This natural consortium

  2. New insights into the early stages of silica-controlled barium carbonate crystallisation.

    PubMed

    Eiblmeier, Josef; Schürmann, Ulrich; Kienle, Lorenz; Gebauer, Denis; Kunz, Werner; Kellermeier, Matthias

    2014-12-21

    Recent work has demonstrated that the dynamic interplay between silica and carbonate during co-precipitation can result in the self-assembly of unusual, highly complex crystal architectures with morphologies and textures resembling those typically displayed by biogenic minerals. These so-called biomorphs were shown to be composed of uniform elongated carbonate nanoparticles that are arranged according to a specific order over mesoscopic scales. In the present study, we have investigated the circumstances leading to the continuous formation and stabilisation of such well-defined nanometric building units in these inorganic systems. For this purpose, in situ potentiometric titration measurements were carried out in order to monitor and quantify the influence of silica on both the nucleation and early growth stages of barium carbonate crystallisation in alkaline media at constant pH. Complementarily, the nature and composition of particles occurring at different times in samples under various conditions were characterised ex situ by means of high-resolution electron microscopy and elemental analysis. The collected data clearly evidence that added silica affects carbonate crystallisation from the very beginning (i.e. already prior to, during, and shortly after nucleation), eventually arresting growth on the nanoscale by cementation of BaCO3 particles within a siliceous matrix. Our findings thus shed light on the fundamental processes driving bottom-up self-organisation in silica-carbonate materials and, for the first time, provide direct experimental proof that silicate species are responsible for the miniaturisation of carbonate crystals during growth of biomorphs, hence confirming previously discussed theoretical models for their formation mechanism. PMID:25362999

  3. Precipitation Indices Low Countries

    NASA Astrophysics Data System (ADS)

    van Engelen, A. F. V.; Ynsen, F.; Buisman, J.; van der Schrier, G.

    2009-09-01

    Since 1995, KNMI published a series of books(1), presenting an annual reconstruction of weather and climate in the Low Countries, covering the period AD 763-present, or roughly, the last millennium. The reconstructions are based on the interpretation of documentary sources predominantly and comparison with other proxies and instrumental observations. The series also comprises a number of classifications. Amongst them annual classifications for winter and summer temperature and for winter and summer dryness-wetness. The classification of temperature have been reworked into peer reviewed (2) series (AD 1000-present) of seasonal temperatures and temperature indices, the so called LCT (Low Countries Temperature) series, now incorporated in the Millennium databases. Recently we started a study to convert the dryness-wetness classifications into a series of precipitation; the so called LCP (Low Countries Precipitation) series. A brief outline is given here of the applied methodology and preliminary results. The WMO definition for meteorological drought has been followed being that a period is called wet respectively dry when the amount of precipitation is considerable more respectively less than usual (normal). To gain a more quantitative insight for four locations, geographically spread over the Low Countries area (De Bilt, Vlissingen, Maastricht and Uccle), we analysed the statistics of daily precipitation series, covering the period 1900-present. This brought us to the following definition, valid for the Low Countries: A period is considered as (very) dry respectively (very) wet if over a continuous period of at least 60 days (~two months) cq 90 days (~three months) on at least two out of the four locations 50% less resp. 50% more than the normal amount for the location (based on the 1961-1990 normal period) has been measured. This results into the following classification into five drought classes hat could be applied to non instrumental observations: Very wet period (+2): Wide scale river flooding, marshy acres and meadows.-Farmers cope with poor harvests of hay, grains, fruit etc. resulting in famines.-Late grape harvests, poor yield quantity and quality of wine. Wet period (+1): High water levels cq discharges of major rivers, tributaries and brooks, local river floodings, marshy acres and meadows in the low lying areas.-Wearisome and hampered agriculture. Normal (0) Dry period (-1): Low water levels cq discharges of major rivers, tributaries and brooks. Some brooks may dry up.-Summer half year: local short of yield of grass, hay and other forage.-Summer half year: moor-, peat- and forest fires. Very dry period (-2): Very low water levels cq discharges of major rivers and tributaries. Brooks and wells dry up. Serious shortage of drinking water; especially in summer.-Major agricultural damage, shortage of water, mortality stock of cattle. Shortage of grain. Flour can not be produced due to water mills running out of water, shortage of bread, bread riots, famines.-Large scale forest and peat areas, resulting in serious air pollution. Town fires. By verifying the historical evidence on these criterions, a series of 5 step indices ranging from very dry to very wet for summer and winter half year of the Low Countries was obtained. Subsequently these indices series were compared with the instrumentally observed seasonal precipitation sums for De Bilt (1735-2008), which is considered to be representative for the Central Netherlands. For winter (Oct-March) and summer half year (Apr.-Sept.) the accumulated precipitation amounts are calculated; these amounts are approximately normally distributed. Based on this distribution, the cumulative frequency distribution is calculated. By tabulating the number of summers in the pre-instrumental period 1201-1750 for each of the drought classes, a distribution is calculated which is then related to the modern accumulated precipitation distribution. Assuming that the accumulated precipitation amount has not been below (above) the mean precipitation minus (plus) three standard deviations for

  4. Using Barium Ions for Heavy-Atom Derivatization and Phasing of Xylanse ll from Trichoderma longibrachiatum

    SciTech Connect

    Moiseeva,N.; Allaire, M.

    2007-01-01

    This paper describes the use of barium chloride to produce a heavy-atom derivative of xylanase II crystals from Trichoderma longibrachiatum, which was obtained either by cocrystallization or soaking. SAD phasing led to interpretable electron-density maps that allowed unambiguous chain tracing. In the best case, with a data set collected at 9.5 keV, 88% of the residues were built, with 83% of the side chains assigned. The barium ions are found to mainly interact with main-chain carbonyl groups and water molecules. It is suggested that barium ions could also be used as a potential anomalous scatterer in the quick cryosoaking procedure for phasing.

  5. Modeling the crystal distribution of lead-sulfate in lead-acid batteries with 3D spatial resolution

    NASA Astrophysics Data System (ADS)

    Huck, Moritz; Badeda, Julia; Sauer, Dirk Uwe

    2015-04-01

    For the reliability of lead-acid batteries it is important to have an accurate prediction of its response to load profiles. A model for the lead-sulfate growth is presented, which is embedded in a physical-chemical model with 3D spatial resolution is presented which is used for analyzing the different mechanism influencing the cell response. One import factor is the chemical dissolution and precipitation of lead-sulfate, since its dissolution speed limits the charging reaction and the accumulation of indissolvable of lead-sulfate leads to capacity degradation. The cell performance/behavior is not only determined by the amount of the sulfate but also by the radii and distribution of the crystals. The presented model can be used to for an improved understanding of the interaction of the different mechanisms.

  6. Scintillation properties of lead sulfate

    SciTech Connect

    Moses, W.W.; Derenzo, S.E. ); Shlichta, P.J. )

    1991-11-01

    We report on the scintillation properties of lead sulfate (PbSO{sub 4}), a scintillator that show promise as a high energy photon detector. It physical properties are well suited for gamma detection, as its has a density of 6.4 gm/cm{sup 3}, a 1/e attenuation length for 511 keV photons of 1.2 cm, is not affected by air or moisture, and is cut and polished easily. In 99.998% pure PbSO{sub 4} crystals at room temperature excited by 511 keV annihilation photons, the fluorescence decay lifetime contains significant fast components having 1.8 ns (5%) and 19 ns (36%) decay times, but with longer components having 95 ns (36%) and 425 ns (23%) decays times. The peak emission wavelength is 335 nm, which is transmitted by borosilicate glass windowed photomultiplier tubes. The total scintillation light output increases with decreasing temperature fro 3,200 photons/MeV at +45{degrees}C to 4, 900 photons/MeV at room temperature (+25{degrees}C) and 68,500 photons/MeV at {minus}145{degrees}C. In an imperfect, 3 mm cube of a naturally occurring mineral form of PbSO{sub 4} (anglesite) at room temperature, a 511 keV photopeak is seen with a total light output of 60% that BGO. There are significant sample to sample variations of the light output among anglesite samples, so the light output of lead sulfate may improve when large synthetic crystals become available. 10 refs.

  7. Magnetic properties of Ni substituted Y-type barium ferrite

    NASA Astrophysics Data System (ADS)

    Won, Mi Hee; Kim, Chul Sung

    2014-05-01

    Y-type barium hexaferrite is attractive material for various applications, such as high frequency antennas and RF devices, because of its interesting magnetic properties. Especially, Ni substituted Y- type hexaferrites have higher magnetic ordering temperature than other Y-type. We have investigated macroscopic and microscopic properties of Y-type barium hexaferrite. Ba2Co2-xNixFe12O22 (x = 0, 0.5, 1.0, 1.5, and 2.0) samples are prepared by solid-state reaction method and studied by X-ray diffraction (XRD), vibrating sample magnetometer, and Mössbauer spectroscopy, as well as a network analyzer for high frequency characteristics. The XRD pattern is analyzed by Rietveld refinement method and confirms the hexagonal structure with R-3m. The hysteresis curve shows ferrimagnetic behavior. Saturation magnetization (Ms) decreases with Ni contents. Ni2+, which preferentially occupies the octahedral site with up-spin sub-lattice, has smaller spin value S of 1 than Co2+ having S = 3/2. The zero-field-cooled (ZFC) measurement of Ba2Co1.5Ni0.5Fe12O22 shows that Curie and spin transition temperatures are found to be 718 K and 209 K, respectively. The Curie temperature TC is increased with Ni contents, while TS is decreased with Ni. The Mössbauer spectra were measured at various temperatures and fitted by using a least-squares method with six sextet of six Lorentzian lines for Fe sites, corresponding to the 3bVI, 6cIV*, 6cVI, 18hVI, 6cIV, and 3aIV sites at below TC. From Mössbauer measurements, we confirmed the spin state of Fe ion to be Fe3+ and obtained the isomer shift (?), magnetic hyperfine field (Hhf), and the occupancy ratio of Fe ions at six sub-lattices. The complex permeability and permittivity are measured between 100 MHz and 4 GHz, suggesting that Y-type barium hexaferrite is promising for antenna applications in UHF band.

  8. Magnetic properties of Ni substituted Y-type barium ferrite

    SciTech Connect

    Won, Mi Hee; Kim, Chul Sung

    2014-05-07

    Y-type barium hexaferrite is attractive material for various applications, such as high frequency antennas and RF devices, because of its interesting magnetic properties. Especially, Ni substituted Y- type hexaferrites have higher magnetic ordering temperature than other Y-type. We have investigated macroscopic and microscopic properties of Y-type barium hexaferrite. Ba{sub 2}Co{sub 2?x}Ni{sub x}Fe{sub 12}O{sub 22} (x?=?0, 0.5, 1.0, 1.5, and 2.0) samples are prepared by solid-state reaction method and studied by X-ray diffraction (XRD), vibrating sample magnetometer, and Mössbauer spectroscopy, as well as a network analyzer for high frequency characteristics. The XRD pattern is analyzed by Rietveld refinement method and confirms the hexagonal structure with R-3m. The hysteresis curve shows ferrimagnetic behavior. Saturation magnetization (M{sub s}) decreases with Ni contents. Ni{sup 2+}, which preferentially occupies the octahedral site with up-spin sub-lattice, has smaller spin value S of 1 than Co{sup 2+} having S?=?3/2. The zero-field-cooled (ZFC) measurement of Ba{sub 2}Co{sub 1.5}Ni{sub 0.5}Fe{sub 12}O{sub 22} shows that Curie and spin transition temperatures are found to be 718?K and 209?K, respectively. The Curie temperature T{sub C} is increased with Ni contents, while T{sub S} is decreased with Ni. The Mössbauer spectra were measured at various temperatures and fitted by using a least-squares method with six sextet of six Lorentzian lines for Fe sites, corresponding to the 3b{sub VI}, 6c{sub IV}*, 6c{sub VI}, 18h{sub VI}, 6c{sub IV}, and 3a{sub IV} sites at below T{sub C}. From Mössbauer measurements, we confirmed the spin state of Fe ion to be Fe{sup 3+} and obtained the isomer shift (?), magnetic hyperfine field (H{sub hf}), and the occupancy ratio of Fe ions at six sub-lattices. The complex permeability and permittivity are measured between 100?MHz and 4?GHz, suggesting that Y-type barium hexaferrite is promising for antenna applications in UHF band.

  9. Ruthenium and hafnium abundances in giant and dwarf barium stars

    E-print Network

    D. M. Allen; G. F. Porto de Mello

    2007-08-13

    We present abundances for Ru and Hf, compare them to abundances of other heavy elements, and discuss the problems found in determining Ru and Hf abundances with laboratory gf-values in the spectra of barium stars. We determined Ru and Hf abundances in a sample of giant and dwarf barium stars, by the spectral synthesis of two RuI (4080.574A and 4757.856A) and two HfII (4080.437A and 4093.155A) transitions. The stellar spectra were observed with FEROS/ESO, and the stellar atmospheric parameters lie in the range 4300 < Teff/K < 6500, -1.2 < [Fe/H] <= 0 and 1.4 <= log g < 4.6. The HfII 4080A and the RuI 4758A observed transitions result in a unreasonably high solar abundance, given certain known uncertainties, when fitted with laboratory gf-values. For these two transitions we determined empirical gf-values by fitting the observed line profiles of the spectra of the Sun and Arcturus. For the sample stars, this procedure resulted in a good agreement of Ru and Hf abundances given by the two available lines. The resulting Ru and Hf abundances were compared to those of Y, Nd, Sm and Eu. In the solar system Ru, Sm and Eu are dominated by the r-process and Hf, Nd and Y by the s-process, and all of these elements are enhanced in barium stars since they lie inside the s-process path. Ru abundances show large scatter when compared to other heavy elements, whereas Hf abundances show less scatter and closely follow the abundances of Sm and Nd, in good agreement with theoretical expectations. We also suggest a possible, unexpected, correlation of Ru and Sm abundances. The observed behaviour in abundances is probably due to variations in the 13C pocket efficiency in AGB stars, and, though masked by high uncertainties, hint at a more complex scenario than proposed by theory.

  10. Storm-wide precipitation retrievals

    E-print Network

    Loparo, Jessica A. (Jessica Ann), 1980-

    2004-01-01

    The monitoring of precipitation is important for scientific purposes, such as the study of world weather patterns, the development of global precipitation maps, and the tracking of seasonal and diurnal variations in ...

  11. Sulfate induced heave in lime stabilized soil 

    E-print Network

    Bredenkamp, Sanet

    1994-01-01

    The addition of hydrated lime to clay soils is one of the most common methods of soil stabilization. However, when sulfates are present in the soil, the calcium in the lime reacts with the sulfates to form ettringite, an expandable mineral...

  12. Sulfate reduction in deep-sea sediments

    NASA Technical Reports Server (NTRS)

    Canfield, D. E.

    1991-01-01

    Sulfate reduction rates calculated from about 200 DSDP pore water sulfate profiles have been contoured and plotted on a map covering most areas of the world ocean. Rates show a remarkable spatial consistency, with high rates observed near the continental margins, becoming progressively lower toward the central ocean basins. Relatively elevated rates are also found in the eastern equatorial Pacific, a site of upwelling and correspondingly high rates of primary organic production. Overall, the distribution of sulfate reduction in pelagic sediments looks very similar to the distribution of primary organic carbon production. When rates are directly compared, however, the correlation between sulfate reduction and primary production is only moderately strong. Perhaps the most important influence on sulfate reduction is sediment deposition rate and the control this has over the fraction of the sedimentary organic carbon flux that becomes available for sulfate reduction. The slower the rate of sediment deposition the more time for oxic respiration and the less organic carbon that escapes to the zone of sulfate reduction. To predict most accurately sulfate reduction rates, however, the variables of primary production, water depth, and sediment deposition rate must all be integrated.

  13. 21 CFR 582.1643 - Potassium sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Potassium sulfate. 582.1643 Section 582.1643 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE General Purpose Food Additives § 582.1643 Potassium sulfate. (a)...

  14. 21 CFR 558.364 - Neomycin sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... Escherichia coli susceptible to neomycin. To provide 10 milligrams (mg) of neomycin sulfate per pound of body... disease signs, and environmental temperature and humidity, each of which affects feed consumption. If... replacer. Do. To provide 10 mg of neomycin sulfate per pound of body weight per day for a maximum of...

  15. Integrated Spectroscopic Studies of Anhydrous Sulfate Minerals

    NASA Technical Reports Server (NTRS)

    Lane, M. D.; Bishop, J. L.; Dyar, M. D.; Cloutis, E.; Forray, F. L.; Hiroi, T.

    2005-01-01

    Sulfates have been identified in Martian soils and bedrock and are emerging as an important indicator for aqueous activity on Mars. Sulfate minerals can form in a variety of low-temperature (evaporitic; chemical-weathering) and high-temperature (volcanic/fumarolic; hydrothermal) environments and their formational environments can range from alkaline to acidic. Although sulfates generally form in the presence of water, not all sulfates are hydrous or contain water in their structures. Many of these anhydrous sulfates (Dana group 28; Strunz class 67A) are minerals that form as accompanying phases to the main minerals in ore deposits or as replacement deposits in sedimentary rocks. However, some form from thermal decomposition of OH or H2O-bearing sulfates, such as from the reaction [1]: jarosite = yavapaiite + Fe2O3 + H2O. Where known, the stability fields of these minerals all suggest that they would be stable under martian surface conditions [2]. Thus, anhydrous sulfate minerals may contribute to martian surface mineralogy, so they must be well-represented in spectral libraries used for interpretation of the Martian surface. We present here the preliminary results of an integrated study of emittance, reflectance, and Mossbauer spectroscopy of a suite of wel-lcharacterized anhydrous sulfates.

  16. Precipitation hardening austenitic superalloys

    DOEpatents

    Korenko, Michael K. (Wexford, PA)

    1985-01-01

    Precipitation hardening, austenitic type superalloys are described. These alloys contain 0.5 to 1.5 weight percent silicon in combination with about 0.05 to 0.5 weight percent of a post irradiation ductility enhancing agent selected from the group of hafnium, yttrium, lanthanum and scandium, alone or in combination with each other. In addition, when hafnium or yttrium are selected, reductions in irradiation induced swelling have been noted.

  17. Nickel Solubility and Precipitation in Soils: A Thermodynamic Study

    SciTech Connect

    Peltier,E.; Allada, R.; Navrotsky, A.; Sparks, D.

    2006-01-01

    The formation of mixed-metal-Al layered double hydroxide (LDH) phases similar to hydrotalcite has been identified as a significant mechanism for immobilization of trace metals in some environmental systems. These precipitate phases become increasingly stable as they age, and their formation may therefore be an important pathway for sequestration of toxic metals in contaminated soils. However, the lack of thermodynamic data for LDH phases makes it difficult to model their behavior in natural systems. In this work, enthalpies of formation for Ni LDH phases with nitrate and sulfate interlayers were determined and compared to recently published data on carbonate interlayer LDHs. Differences in the identity of the anion interlayer resulted in substantial changes in the enthalpies of formation of the LDH phases, in the order of increasing enthalpy carbonate<sulfateprecipitates. Both mechanical mixture and solid-solution models could be used to predict the thermodynamic properties of the LDH phases. Modeling results based on these thermodynamic data indicated that the formation of LDH phases on soil mineral substrates decreased Ni solubility compared to Ni(OH)2 over pH 5-9 when soluble Al is present in the soil substrate. Over time, both of these precipitate phases will transform to more stable Ni phyllosilicates.

  18. Crystallization of Chicken Egg White Lysozyme from Assorted Sulfate Salts

    NASA Technical Reports Server (NTRS)

    Forsythe, Elizabeth L.; Snell, Edward H.; Malone, Christine C.; Pusey, Marc L.

    1999-01-01

    Chicken egg white lysozyme has been found to crystallize from ammonium, sodium, potassium, rubidium, magnesium, and manganese sulfates at acidic and basic pH, with protein concentrations from 60 to 190 mg/ml. Crystals have also been grown at 4 C in the absence of any other added salts using isoionic lysozyme which was titrated to pH 4.6 with dilute sulfuric acid. Four different crystal forms have been obtained, depending upon the temperature, protein concentration, and precipitating salt employed. Crystals grown at 15 C were generally tetragonal, with space group P4(sub 3)2(sub 1)2. Crystallization at 20 C typically resulted in the formation of orthorhombic crystals, space group P2(sub 1)2(sub 1)2(sub 1). The tetragonal reversible reaction orthorhombic transition appeared to be a function of both the temperature and protein concentration, occurring between 15 and 20 C and between 100 and 125 mg/ml protein concentration. Crystallization from 1.2 M magnesium sulfate at pH 7.8 gave a trigonal crystal, space group P3(sub 1)2(sub 1), a = b = 87.4, c = 73.7, gamma = 120 deg, which diffracted to 2.8 A. Crystallization from ammonium sulfate at pH 4.6, generally at lower temperatures, was also found to result in a monoclinic form. space group C2, a = 65.6, b = 95.0, c = 41.2, beta = 119.2 deg. A crystal of approximately 0.2 x 0.2 x 0.5 mm grown from bulk solution diffracted to approximately 3.5 A.

  19. Uncertainties in Arctic Precipitation

    NASA Astrophysics Data System (ADS)

    Majhi, I.; Alexeev, V. A.; Cherry, J. E.; Cohen, J. L.; Groisman, P. Y.

    2012-12-01

    Arctic precipitation is riddled with measurement biases; to address the problem is imperative. Our study focuses on comparison of various datasets and analyzing their biases for the region of Siberia and caution that is needed when using them. Five sources of data were used ranging from NOAA's product (RAW, Bogdanova's correction), Yang's correction technique and two reanalysis products (ERA-Interim and NCEP). The reanalysis dataset performed better for some months in comparison to Yang's product, which tends to overestimate precipitation, and the raw dataset, which tends to underestimate. The sources of bias vary from topography, to wind, to missing data .The final three products chosen show higher biases during the winter and spring season. Emphasis on equations which incorporate blizzards, blowing snow and higher wind speed is necessary for regions which are influenced by any or all of these factors; Bogdanova's correction technique is the most robust of all the datasets analyzed and gives the most reasonable results. One of our future goals is to analyze the impact of precipitation uncertainties on water budget analysis for the Siberian Rivers.

  20. Passive abatement of acid rock drainage by sulfate reducing bacteria

    SciTech Connect

    Thompson, D.N.; Sayer, R.L.; Noah, K.S.

    1996-10-01

    Passive treatment systems for Acid Rock Drainage (ARD) using wetland technology have been in development at eastern coal mines since the mid 1980s. Due to the high altitudes, remoteness, lack of large flat areas, and/or heavy metal levels at western mine sites, application of this technology has been lacking. This research explored whether pine sawdust can be used as sole carbon source in a smaller volume system for ARD remediation which can handle high throughputs. The technology utilizes sulfate reducing bacteria (SRB) to precipitate metal sulfides from their sulfates, while raising pH due to net consumption of H{sup +}. Laboratory results indicate that indigenous SRB are present in mud obtained from a northern Idaho mine site. With partially degraded lodgepole pine sawdust as carbon source, 50-99% reduction of various metals, and pH increases from 3 to about 7 were attained in ARD collected from mine seeps. Thus, this system appears promising as a long term, low cost/maintenance technology for ARD remediation at remote western mines.