Science.gov

Sample records for ammonium tungstates

  1. Effect of Substrate Temperature on the Properties of Sprayed WO3 Thin Films Using Peroxotungstic Acid and Ammonium Tungstate: A Comparative Study

    NASA Astrophysics Data System (ADS)

    Ganbavle, V. V.; Kim, J. H.; Rajpure, K. Y.

    2015-03-01

    A comparative study on the physicochemical properties of tungsten oxide (WO3) thin films synthesized using peroxotungstic acid (PTA) and ammonium tungstate (AT) by simple spray pyrolysis technique is reported. X-ray diffraction patterns show that the films deposited using both the precursors are polycrystalline with monoclinic crystal structure. The x-ray photoelectron spectroscopy studies confirm that the films are sub-stoichiometric with O/W ratios of 2.93 and 2.87, respectively, for typical PTA and AT films. Tungsten (W) exists in two chemical states, 5+ and 6+. Scanning electron microscopy images show the uniform and dense network of wires in PTA films, while the films deposited using AT possess a porous structure with small grains. Electrical and dielectric studies show that films are highly resistive and possess high dielectric constant. The near ultra-violet, blue, green and weak red emissions due to defects were observed in the photoluminescence studies. Properties of the WO3 thin films reported here are suitable for gas sensor applications. Films deposited using PTA are more functional than those deposited using AT.

  2. Femtosecond laser ablation of cadmium tungstate for scintillator arrays

    NASA Astrophysics Data System (ADS)

    Richards, S.; Baker, M. A.; Wilson, M. D.; Lohstroh, A.; Seller, P.

    2016-08-01

    Ultrafast pulsed laser ablation has been investigated as a technique to machine CdWO4 single crystal scintillator and segment it into small blocks with the aim of fabricating a 2D high energy X-ray imaging array. Cadmium tungstate (CdWO4) is a brittle transparent scintillator used for the detection of high energy X-rays and γ-rays. A 6 W Yb:KGW Pharos-SP pulsed laser of wavelength 1028 nm was used with a tuneable pulse duration of 10 ps to 190 fs, repetition rate of up to 600 kHz and pulse energies of up to 1 mJ was employed. The effect of varying the pulse duration, pulse energy, pulse overlap and scan pattern on the laser induced damage to the crystals was investigated. A pulse duration of ≥500 fs was found to induce substantial cracking in the material. The laser induced damage was minimised using the following operating parameters: a pulse duration of 190 fs, fluence of 15.3 J cm-2 and employing a serpentine scan pattern with a normalised pulse overlap of 0.8. The surface of the ablated surfaces was studied using scanning electron microscopy, energy dispersive X-ray spectroscopy, atomic force microscopy and X-ray photoelectron spectroscopy. Ablation products were found to contain cadmium tungstate together with different cadmium and tungsten oxides. These laser ablation products could be removed using an ammonium hydroxide treatment.

  3. Vanadate, molybdate and tungstate for orthomolecular medicine.

    PubMed

    Matsumoto, J

    1994-09-01

    Recent studies indicate that oxyanions, such as vanadate (V) or vanadyl (IV), cause insulin-like effects on rats by stimulating the insulin receptor tyrosine kinase. Tungstate (VI) and molybdate (VI) show the same effects on rat adipocytes and hepatocytes. Results of uncontrolled trials on volunteers accumulated in Japan also suggest that tungstate effectively regulates diabetes mellitus without detectable side effects. Since these oxyanions naturally exist in organisms, oxyanion therapy, the oral administration of vanadate, vanadyl, molybdate, or tungstate, can be considered to be orthomolecular medicine. Therefore, these oxyanions may provide a viable alternative to chemotherapy. Many diseases in addition to diabetes mellitus might also be treated since the implication of these results is that tyrosine kinases are involved in a variety of diseases. PMID:7815975

  4. Morphology Tuning of Strontium Tungstate Nanoparticles

    SciTech Connect

    Joseph, S.; George, T.; George, K. C.; Sunny, A. T.; Mathew, S.

    2007-08-22

    Strontium tungstate nanocrystals in two different morphologies are successfully synthesized by controlled precipitation in aqueous and in poly vinyl alcohol (PVA) medium. Structural characterizations are carried out by XRD and SEM. The average particle size calculated for the SrWO4 prepared in the two different solvents ranges 20-24 nm. The SEM pictures show that the surface morphologies of the SrWO4 nanoparticles in aqueous medium resemble mushroom and the SrWO4 nanoparticles in PVA medium resemble cauliflower. Investigations on the room temperature luminescent properties of the strontium tungstate nanoparticles prepared in aqueous and PVA medium shows strong emissions around 425 nm.

  5. Synthesis procedure optimization and characterization of europium (III) tungstate nanoparticles

    NASA Astrophysics Data System (ADS)

    Rahimi-Nasrabadi, Mehdi; Pourmortazavi, Seied Mahdi; Ganjali, Mohammad Reza; Reza Banan, Ali; Ahmadi, Farhad

    2014-09-01

    Taguchi robust design as a statistical method was applied for the optimization of process parameters in order to tunable, facile and fast synthesis of europium (III) tungstate nanoparticles. Europium (III) tungstate nanoparticles were synthesized by a chemical precipitation reaction involving direct addition of europium ion aqueous solution to the tungstate reagent solved in an aqueous medium. Effects of some synthesis procedure variables on the particle size of europium (III) tungstate nanoparticles were studied. Analysis of variance showed the importance of controlling tungstate concentration, cation feeding flow rate and temperature during preparation of europium (III) tungstate nanoparticles by the proposed chemical precipitation reaction. Finally, europium (III) tungstate nanoparticles were synthesized at the optimum conditions of the proposed method. The morphology and chemical composition of the prepared nano-material were characterized by means of X-ray diffraction, scanning electron microscopy, transmission electron microscopy, FT-IR spectroscopy and fluorescence.

  6. Electrosynthesis and characterization of zinc tungstate nanoparticles

    NASA Astrophysics Data System (ADS)

    Rahimi-Nasrabadi, Mehdi; Pourmortazavi, Seied Mahdi; Ganjali, Mohammad Reza; Hajimirsadeghi, Seiedeh Somayyeh; Zahedi, Mir Mahdi

    2013-09-01

    Zinc tungstate nanoparticles with different sizes are produced through an electrolysis process including a zinc plate anode in sodium tungstate solution. The shape and size of the product was found to be controlled by varying reaction parameters such as electrolysis voltage, stirring rate of electrolyte solution and temperature. The morphological (SEM) characterization analysis was performed on the product and UV-Vis spectrophotometry and FT-IR spectroscopy was utilized to characterize the electrodeposited nanoparticles. Study of the particle size of the product versus the electrolysis voltage showed that, increasing the voltage from 4 to 8 V, led to the particle size of zinc tungstate to decrease, but further increasing the voltage from 8 to 12 V, the particle size of the produced particles increased. The size and shape of the product was also found to be dependent on the stirring rate and temperature of the electrolyte solution. X-ray diffraction (XRD), scanning electron microscopy (SEM), FT-IR spectroscopy, and photoluminescence, were used to study the structure as well as composition of the nano-material prepared under optimum conditions.

  7. Ammonium acetate

    Integrated Risk Information System (IRIS)

    Ammonium acetate ; CASRN 631 - 61 - 8 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

  8. Ammonium methacrylate

    Integrated Risk Information System (IRIS)

    Ammonium methacrylate ; CASRN 16325 - 47 - 6 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 Noncarcin

  9. Ammonium sulfamate

    Integrated Risk Information System (IRIS)

    Ammonium sulfamate ; CASRN 7773 - 06 - 0 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 Noncarcinogen

  10. 40 CFR 721.9840 - Tungstate (W12(OH)2O386-) hexasodium (9CI).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Tungstate (W12(OH)2O386-) hexasodium... Specific Chemical Substances § 721.9840 Tungstate (W12(OH)2O386-) hexasodium (9CI). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as tungstate...

  11. 40 CFR 721.9840 - Tungstate (W12(OH)2O386-) hexasodium (9CI).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Tungstate (W12(OH)2O386-) hexasodium... Specific Chemical Substances § 721.9840 Tungstate (W12(OH)2O386-) hexasodium (9CI). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as tungstate...

  12. Tuning the architecture and properties of microstructured yttrium tungstate oxide hydroxide and lanthanum tungstate.

    PubMed

    Kaczmarek, Anna M; Liu, Ying-Ya; Van der Voort, Pascal; Van Deun, Rik

    2013-04-21

    In this paper, various microstructures of yttrium and lanthanum tungstates were synthesized under hydrothermal conditions, at pH 5, in a ligand-free environment, and in the presence of a dioctyl sodium sulfosuccinate (DSS) surfactant. It was observed that the shape of the nanobuilding blocks, and therefore the architecture of the microstructures, could be tuned by controlling the reaction conditions, such as the source of the rare earth, the amount of a surfactant and the reaction time. X-ray powder diffraction (XRD), elemental analysis, scanning electron microscopy (SEM), and N2 adsorption were employed to characterize the obtained products. The photoluminescent properties of Eu(3+) and Dy(3+) doped tungstate materials were investigated. Luminescence measurements showed an efficient charge transfer from the WO4(2-) groups to Eu(3+) and Dy(3+) ions. It was found that under UV excitation the Dy(3+) doped Y(WO3)2(OH)3 and La2(WO4)3 precursors exhibit white emission. PMID:23426044

  13. In situ growth of epitaxial cerium tungstate (100) thin films.

    PubMed

    Skála, Tomáš; Tsud, Nataliya; Orti, Miguel Ángel Niño; Menteş, Tevfik Onur; Locatelli, Andrea; Prince, Kevin Charles; Matolín, Vladimír

    2011-04-21

    The deposition of ceria on a preoxidized W(110) crystal at 870 K has been studied in situ by photoelectron spectroscopy and low-energy electron diffraction. Formation of an epitaxial layer of crystalline cerium tungstate Ce(6)WO(12)(100), with the metals in the Ce(3+) and W(6+) chemical states, has been observed. The interface between the tungsten substrate and the tungstate film consists of WO suboxide. At thicknesses above 0.89 nm, cerium dioxide grows on the surface of Ce(6)WO(12), favoured by the limited diffusion of tungsten from the substrate. PMID:21399780

  14. Synthesis of potassium tungstate micro-walls by thermal evaporation

    NASA Astrophysics Data System (ADS)

    Hong, Kunquan; Xie, Maohai; Hu, Rong; Wu, Huasheng

    2006-09-01

    We report the synthesis of potassium tungstate (K 2W 3O 10) micro-walls by a simple method of thermal evaporation. Using tungsten powder, tungsten oxide powder and potassium iodide as the source materials and tungsten plate as the substrate, K 2W 3O 10 micro-walls with thicknesses ranging from 400 nm to 2 μm, lengths up to hundreds of micrometers and heights up to tens of micrometers are obtained on a large scale. The possible mechanism for the formation of these tungstate micro-walls is discussed.

  15. Synchrotron-based far-infrared spectroscopy of nickel tungstate

    NASA Astrophysics Data System (ADS)

    Kalinko, A.; Kuzmin, A.; Roy, P.; Evarestov, R. A.

    2016-07-01

    Monoclinic antiferromagnetic NiWO4 was studied by far-infrared (30-600 cm-1) absorption spectroscopy in the temperature range of 5-300 K using the synchrotron radiation from SOLEIL source. Two isomorphous CoWO4 and ZnWO4 tungstates were investigated for comparison. The phonon contributions in the far-infrared range of tungstates were interpreted using the first-principles spin-polarized linear combination of atomic orbital calculations. No contributions from magnetic excitations were found in NiWO4 and CoWO4 below their Neel temperatures down to 5 K.

  16. Growth of transition metals on cerium tungstate model catalyst layers.

    PubMed

    Skála, T; Tsud, N; Stetsovych, V; Mysliveček, J; Matolín, V

    2016-10-01

    Two model catalytic metal/oxide systems were investigated by photoelectron spectroscopy and scanning tunneling microscopy. The mixed-oxide support was a cerium tungstate epitaxial thin layer grown in situ on the W(1 1 0) single crystal. Active particles consisted of palladium and platinum 3D islands deposited on the tungstate surface at 300 K. Both metals were found to interact weakly with the oxide support and the original chemical state of both support and metals was mostly preserved. Electronic and morphological changes are discussed during the metal growth and after post-annealing at temperatures up to 700 K. Partial transition-metal coalescence and self-cleaning from the CO and carbon impurities were observed. PMID:27494195

  17. Laser system with trivalent chromium doped aluminum tungstate fluorescent converter

    SciTech Connect

    Dube, G.

    1988-09-06

    This patent describes a laser system combination comprising: (a) a neodymium element; (b) a light source for pumping the neodymium laser element to produce coherent, monochromatic light; (c) a fluorescent converter element positioned in light exchange relationship with the light source for spectrally shifting at least a portion of light outside of the neodymium laser pumping band passing through the neodymium laser into light in the neodymium laser pumping band; (d) the fluorescent element including trivalent chromium doped aluminum tungstate excited by light passing through the laser which is outside of the pumping band for the laser, the tungstate covering a portion of light passing through the laser element which is outside of the pumping band into light within the pumping band; (e) the concentration of the trivalent chromium dopant lying in the range of 0.5 to 3 per mole percent (%).

  18. Structure and thermal behavior of zirconium tungstate under heating

    NASA Astrophysics Data System (ADS)

    Dedova, E. S.; Shutilova, E. S.; Geber, R.; Gomze, L. A.; Kulkov, S. N.

    2016-07-01

    The morphology and properties of powders ZrW2O7(OH)2·2H2O and ZrW2O8, obtained under the conditions of hydrothermal synthesis was studied. Using the high-temperature X-ray analysis, the mechanism of formation of zirconium tungstate was established. The influence of temperature on the structure and properties of materials was studied using shadow-casting method.

  19. Polyimide nanocomposites based on cubic zirconium tungstate

    NASA Astrophysics Data System (ADS)

    Ramasubramanian Sharma, Gayathri

    2009-12-01

    In this research, cubic zirconium tungstate (ZrW2O8) was used as a filler to reduce the CTE of polyimides (PI), and the effect of ZrW2O8 nanoparticles on the bulk polymer properties was studied. Polyimides are high performance polymers with exceptional thermal stability, and there is a need for PIs with low CTEs for high temperature applications. The nanofiller, cubic ZrW2O8, is well known for its isotropic negative thermal expansion (NTE) over a wide temperature range from -272.7 to 777°C. The preparation of nanocomposites involved the synthesis of ZrW 2O8 nanofiller, engineering the polymer-filler interface using linker groups and optimization of processing strategies to prepare free-standing PI nanocomposite films. A hydrothermal method was used to synthesize ZrW 2O8 nanoparticles. Polyimide-ZrW2O8 interface interaction was enhanced by covalently bonding linker moieties to the surface of ZrW2O8 nanoparticles. Specifically, ZrW 2O8 nanoparticles were functionalized with two different linker groups: (1) a short aliphatic silane, and (2) low molecular weight PI. The surface functionalization was confirmed using X-ray photoelectron spectroscopy and thermal gravimetric analysis (TGA). Reprecipitation blending was used to prepare the freestanding PI-ZrW2O8 nanocomposite films with up to 15 volume% filler loading. SEM images showed the improvements in polymer-filler wetting behavior achieved using interface engineering. SEM images indicated that there was better filler dispersion in the PI matrix using reprecipitation blending, compared to the filler dispersion achieved in the nanocomposites prepared using conventional blending technique. The structure-property relationships in PI-ZrW2O8 nanocomposites were investigated by studying the thermal degradation, glass transition, tensile and thermal expansion properties of the nanocomposites. The properties were studied as a function of filler loading and interface linker groups. Addition of ZrW2O8 nanoparticles did not

  20. A functional leptin system is essential for sodium tungstate antiobesity action.

    PubMed

    Canals, Ignasi; Carmona, María C; Amigó, Marta; Barbera, Albert; Bortolozzi, Analía; Artigas, Francesc; Gomis, Ramon

    2009-02-01

    Sodium tungstate is a novel agent in the treatment of obesity. In diet-induced obese rats, it is able to reduce body weight gain by increasing energy expenditure. This study evaluated the role of leptin, a key regulator of energy homeostasis, in the tungstate antiobesity effect. Leptin receptor-deficient Zucker fa/fa rats and leptin-deficient ob/ob mice were treated with tungstate. In lean animals, tungstate administration reduced body weight gain and food intake and increased energy expenditure. However, in animals with deficiencies in the leptin system, treatment did not modify these parameters. In ob/ob mice in which leptin deficiency was restored through adipose tissue transplantation, treatment restored the tungstate-induced body weight gain and food intake reduction as well as energy expenditure increase. Furthermore, in animals in which tungstate administration increased energy expenditure, changes in the expression of key genes involved in brown adipose tissue thermogenesis were detected. Finally, the gene expression of the hypothalamic neuropeptides, Npy, Agrp, and Cart, involved in the leptin regulation of energy homeostasis, was also modified by tungstate in a leptin-dependent manner. In summary, the results indicate that the effectiveness of tungstate in reducing body weight gain is completely dependent on a functional leptin system. PMID:18845634

  1. Synthesis of europium-activated calcium tungstate phosphor

    NASA Astrophysics Data System (ADS)

    Popovici, Elisabeth-Jeanne; Forgaciu, Flavia; Nemes, Miloslava; Ursu, Veronica

    1998-07-01

    The purpose of this study is to establish the way in which different synthesis conditions influence on the structural and luminescent characteristics of europium activated calcium tungstate powder phosphor. CaWO4:Eu3+ samples were prepared by thermal synthesis from mixtures consisting of precipitated-CaWO4, equivalent amounts of Eu2O3 and WO3 (activating system) and CaCl2 or Na2WO4 as flux. Calcination was performed at 800 - 1000 degree(s)C for 2 h, in air. The crystalline structure (XRD-patterns) and luminescent characteristics (emission and excitation spectra of phosphor samples were determined and interpreted.

  2. Tungstate as a Transition State Analog for Catalysis by Alkaline Phosphatase.

    PubMed

    Peck, Ariana; Sunden, Fanny; Andrews, Logan D; Pande, Vijay S; Herschlag, Daniel

    2016-07-01

    The catalytic mechanisms underlying Escherichia coli alkaline phosphatase's (AP) remarkable rate enhancement have been probed extensively. Past work indicated that whereas the serine nucleophile (Ser102) electrostatically repels the product phosphate, another oxyanion, tungstate, binds more strongly in the presence of Ser102. These results predict a covalent bond between the serine nucleophile and tungstate, a model that we test herein. The crystal structure of tungstate-bound alkaline phosphatase provides evidence for a covalent adduct model and further shows that the ligand adopts trigonal bipyramidal geometry, which is infrequently observed for tungstate in small molecules and other active sites but mirrors the geometry of the presumed phosphoryl transfer transition state. The AP active site is known to stabilize another oxyanion, vanadate, in trigonal bipyramidal geometry, but the extent to which binding of either ligand reproduces the energetics of the transition state cannot be deduced from structural inspection alone. To test for transition state analog behavior, we determined the relationship between catalytic activity and affinity for tungstate and vanadate for a series of 20 AP variants. Affinity and activity were highly correlated for tungstate (r(2) = 0.89) but not vanadate (r(2) = 0.23), indicating that the tungstate•AP complex may better mimic this enzyme's transition state properties. The results herein suggest that tungstate will be a valuable tool for further dissecting AP catalysis and may prove helpful in mechanistic studies of other phosphoryl transfer enzymes. PMID:27189921

  3. Toxicity of sodium tungstate to earthworm, oat, radish, and lettuce.

    PubMed

    Bamford, Josie E; Butler, Alicia D; Heim, Katherine E; Pittinger, Charles A; Lemus, Ranulfo; Staveley, Jane P; Lee, K Brian; Venezia, Carmen; Pardus, Michael J

    2011-10-01

    Due to unknown effects of the potential exposure of the terrestrial environment to tungsten substances, a series of toxicity studies of sodium tungstate (Na(2) WO(4) ) was conducted. The effect on earthworm (Eisenia fetida) survival and reproduction was examined using Organisation for Economic Co-operation and Development (OECD) Guideline 222. No effect on either endpoint was seen at the highest concentration tested, resulting in a 56-d no-observed-effect concentration (NOEC) of ≥586 mg tungsten/kg dry soil (nominal concentrations). The effect of sodium tungstate on emergence and growth of plant species was examined according to OECD Guideline 208: oat (Avena sativa), radish (Raphanus sativus), and lettuce (Lactuca sativa). No effects on emergence, shoot height, and dry shoot weight were observed in oats exposed to the highest concentration, resulting in a 21-d NOEC of ≥586 mg tungsten/kg dry soil. The NOECs for radish and lettuce were 65 and 21.7 mg tungsten/kg dry soil (nominal concentrations), respectively. Respective 21-d median effective concentration values (EC50) for radish and lettuce were >586 and 313 mg tungsten/kg dry soil (based on shoot height) (confidence level [CL] -8.5-615); EC25 values were 152 (CL 0-331) and 55 (CL 0-114) mg tungsten/kg dry soil. Results are consistent with the few other tungsten substance terrestrial toxicity studies in the literature. PMID:21805499

  4. Vibrational Spectroscopic Studies on Some Double Alkali Tungstates Belonging to Orthorhombic Class at Room Temperature

    SciTech Connect

    Sharaff, Usha; Bajpai, P. K.; Choudhary, R. N. P.

    2011-11-22

    Room temperature IR and Raman spectra of rubidium lithium tungstate and sodium lithium tungstates belonging to double alkali tungstate family are investigated using group theoretical methods. Observed internal and lattice modes in both systems studied are assigned. Analysis of spectral behavior reveals that the effect of site potential around tungstates ion is weak and the factor group splitting is operative. Differences in the lattice mode mixing and splitting of internal modes is influenced by the statistical ordering between two alkali ions having large and small ionic radii and is explained using size and charge effect observed earlier in scheelite type of structure. Thus, vibrational spectroscopic analysis may be a tool to understand the alkali ion ordering in double alkali systems.

  5. Comparative study of various polyols as complexing agents for the acidimetric titration of tungstate.

    PubMed

    Verchère, J F; Sauvage, J P; Rapaumbya, G R

    1990-05-01

    Most polyols (L = alditol or carbohydrate) form dinuclear tungstate complexes according to the over-all equilibrium 2WO4(2-) + 2H+ + L equal equilibrium [W2O7L]2- + H2O. When the reaction is fast and complete, it allows the acidimetric titration of tungstate. The formation constants of the complexes of a series of polyols were determined by potentiometry. Their values were higher at low ionic strengths. Opposite structural factors govern the stabilities and the formation rates of complexes: alditols of threo configuration react with tungstate faster than those of erythro configuration, but the stability order is erythro greater than threo. Of the polyols investigated, only xylitol and D-glucitol (sorbitol) allowed a fast and accurate potentiometric titration. Using 0.02 M HCl as titrand, 0.04 mmol of tungstate was determined in a volume of 100 cm3. The interference of molybdate is discussed in detail. PMID:2118740

  6. Theoretical calculations of emission of wolframite and scheelite-type tungstate crystals

    SciTech Connect

    Nikolaenko, T.; Hizhnyi, Y.; Nedilko, S.

    2009-01-21

    Tungstate crystals AWO{sub 4} (A = Zn,Cd,Pb) are well-known scintillation materials for various applications in science and technology. In recent years the optical properties of these crystals were intensively studied experimentally and theoretically. However, the origin of luminescence in lead, cadmium and zinc tungstates is still the subject of discussion. According to generally accepted view, the centers of luminescence in AWO{sub 4} crystals are in some or other way related to the tungstate anionic groups. We developed a cluster approach in theoretical investigation of the electronic structure of AWO{sub 4} tungstate crystals based on the configuration interaction (CI) computation in which the lattice vibrations were taken into account.

  7. Large-scale synthesis and photoluminescence of cobalt tungstate nanowires

    NASA Astrophysics Data System (ADS)

    Zhang, Cuiling; Guo, Donglin; Hu, Chenguo; Chen, Yanxue; Liu, Hong; Zhang, Hulin; Wang, Xue

    2013-01-01

    Single-crystalline wolframite-type monoclinic structure cobalt tungstate (CoWO4) nanowires were obtained by a solvothermal method at 180 °C for 24 h with a width of 20 nm and length of 200 to 400 nm. Besides the strong blue-green light emission at 10-250 K, we found much stronger and broader near-infrared emission ranging from 700-1000 nm at about 300 K under the excitation wavelength of 325 nm. The emission and the dependence of emission intensity on temperature are discussed by introducing the effect of Co vacancies. This near-infrared emission material might have potential applications in infrared detection or stealth technology.

  8. Phosphorylation events implicating p38 and PI3K mediate tungstate-effects in MIN6 beta cells

    SciTech Connect

    Piquer, Sandra; Gomis, Ramon . E-mail: rgomis@clinic.ub.es

    2007-06-29

    Oral administration of sodium tungstate is an effective treatment for diabetes in animal models. Several lines of evidence indicate the pancreatic beta cell as one of the targets of tungstate action. Here, we examined the molecular mechanism by which this compound exerts its effects on the beta cell line MIN6. Tungstate treatment induced phosphorylation and subsequent activation of p38 and PI3K which in turn are implicated in tungstate PDX-1 nuclear localization and activation. Although no effect was observed in glucose-induced insulin secretion we found that tungstate activates basal insulin release, a process driven, at least in part, by activation of p38. These results show a direct involvement of p38 and PI3K phosphorylation in the mechanism of action of tungstate in the beta cell.

  9. Effect of sodium tungstate on visual evoked potentials in diabetic rats

    PubMed Central

    Bulut, Mehmet; Dönmez, Barış Özgür; Öztürk, Nihal; Başaranlar, Göksun; Kencebay Manas, Ceren; Derin, Narin; Özdemir, Semir

    2016-01-01

    AIM To evaluate the effect of sodium tungstate on visual evoked potentials (VEPs) in diabetic rats. METHODS Wistar rats were randomly divided into three groups as normal control, diabetic control and diabetic rats treated with sodium tungstate. Diabetes was induced by single intraperitoneal injection of streptozotocin (50 mg/kg). Sodium tungstate [40 mg/(kg·d)] was administered for 12wk and then VEPs were recorded. Additionally, thiobarbituric acid reactive substance (TBARS) levels were measured in brain tissues. RESULTS The latencies of P1, N1, P2, N2 and P3 waves were significantly prolonged in diabetic rats compared with control group. Diabetes mellitus caused an increase in the lipid peroxidation process that was accompanied by changes in VEPs. However, prolonged latencies of VEPs for all components returned to control levels in sodium tungstate-treated group. The treatment of sodium tungstate significantly decreased brain TBARS levels and depleted the prolonged latencies of VEP components compared with diabetic control group. CONCLUSION Sodium tungstate shows protective effects on visual pathway in diabetic rats, and it can be worthy of further study for potential use. PMID:27275420

  10. Sodium tungstate decreases sucrase and Na+/D-glucose cotransporter in the jejunum of diabetic rats.

    PubMed

    Miró-Queralt, Montserrat; Guinovart, Joan J; Planas, Joana M

    2008-09-01

    Sodium tungstate reduces glycemia and reverts the diabetic phenotype in several induced and genetic animal models of diabetes. Oral administration of this compound has recently emerged as an effective treatment for diabetes. Here we examined the effects of 30 days of oral administration of tungstate on disaccharidase and Na+/D-glucose cotransporter (SGLT1) activity in the jejunum of control and streptozotocin-induced diabetic rats. Diabetes increased sucrase-specific activity in the jejunal mucosa but did not affect the activity of lactase, maltase, or trehalase. The abundance and the maximal rate of transport of SGLT1 in isolated brush-border membrane vesicles also increased. Tungstate decreased sucrase activity and normalized SGLT1 expression and activity in the jejunum of diabetic rats. Furthermore, tungstate did not change the affinity of SGLT1 for d-glucose and had no effect on the diffusional component. In control animals, tungstate had no effect on disaccharidases or SGLT1 expression. Northern blot analysis showed that the amount of specific SGLT1 mRNA was the same in the jejunum from all experimental groups, thereby indicating that changes in SGLT1 abundance are due to posttranscriptional mechanisms. We conclude that the antidiabetic effect of tungstate is partly due to normalization of the activity of sucrase and SGLT1 in the brush-border membrane of enterocytes. PMID:18617558

  11. Sodium tungstate induced neurological alterations in rat brain regions and their response to antioxidants.

    PubMed

    Sachdeva, Sherry; Pant, Satish C; Kushwaha, Pramod; Bhargava, Rakesh; Flora, Swaran J S

    2015-08-01

    Tungsten, recognized recently as an environmental contaminant, is being used in arms and ammunitions as substitute to depleted uranium. We studied the effects of sodium tungstate on oxidative stress, few selected neurological variables like acetylcholinesterase, biogenic amines in rat brain regions (cerebral cortex, hippocampus and cerebellum) and their prevention following co-administration of N-acetylcysteine (NAC), naringenin and quercetin. Animals were sub-chronically exposed to sodium tungstate (100 ppm in drinking water) and orally co-supplemented with different antioxidants (0.30 mM) for three months. Sodium tungstate significantly decreased the activity of acetylcholinesterase, dopamine, nor-epinephrine and 5-hydroxytryptamine levels while it increased monoamine oxidase activity in different brain regions. Tungstate exposure produced a significant increase in biochemical variables indicative of oxidative stress while, neurological alterations were more pronounced in the cerebral cortex compared to other regions. Co-administration of NAC and flavonoids with sodium tungstate significantly restored glutathione, prevented changes in the brain biogenic amines, reactive oxygen species (ROS) and TBARS levels in the different brain regions. The protection was more prominent in the animals co-administered with NAC. We can thus conclude that sodium tungstate induced brain oxidative stress and the alterations in some neurological variables can effectively be reduced by co-supplementation of NAC. PMID:25983264

  12. Ammonium nitrate explosive systems

    SciTech Connect

    Coburn, M.D.; Stinecipher, M.M.

    1981-11-17

    Novel explosives which comprise mixtures of ammonium nitrate and an ammonium salt of a nitroazole in desired ratios are disclosed. A preferred nitroazole is 3,5-dinitro-1,2,4-triazole. The explosive and physical properties of these explosives may readily be varied by the addition of other explosives and oxidizers. Certain of these mixtures have been found to act as ideal explosives.

  13. Ammonium nitrate explosive systems

    DOEpatents

    Stinecipher, Mary M.; Coburn, Michael D.

    1981-01-01

    Novel explosives which comprise mixtures of ammonium nitrate and an ammonium salt of a nitroazole in desired ratios are disclosed. A preferred nitroazole is 3,5-dinitro-1,2,4-triazole. The explosive and physical properties of these explosives may readily be varied by the addition of other explosives and oxidizers. Certain of these mixtures have been found to act as ideal explosives.

  14. Tungstate-targeting of BKαβ1 channels tunes ERK phosphorylation and cell proliferation in human vascular smooth muscle.

    PubMed

    Fernández-Mariño, Ana Isabel; Cidad, Pilar; Zafra, Delia; Nocito, Laura; Domínguez, Jorge; Oliván-Viguera, Aida; Köhler, Ralf; López-López, José R; Pérez-García, María Teresa; Valverde, Miguel Ángel; Guinovart, Joan J; Fernández-Fernández, José M

    2015-01-01

    Despite the substantial knowledge on the antidiabetic, antiobesity and antihypertensive actions of tungstate, information on its primary target/s is scarce. Tungstate activates both the ERK1/2 pathway and the vascular voltage- and Ca2+-dependent large-conductance BKαβ1 potassium channel, which modulates vascular smooth muscle cell (VSMC) proliferation and function, respectively. Here, we have assessed the possible involvement of BKαβ1 channels in the tungstate-induced ERK phosphorylation and its relevance for VSMC proliferation. Western blot analysis in HEK cell lines showed that expression of vascular BKαβ1 channels potentiates the tungstate-induced ERK1/2 phosphorylation in a Gi/o protein-dependent manner. Tungstate activated BKαβ1 channels upstream of G proteins as channel activation was not altered by the inhibition of G proteins with GDPβS or pertussis toxin. Moreover, analysis of Gi/o protein activation measuring the FRET among heterologously expressed Gi protein subunits suggested that tungstate-targeting of BKαβ1 channels promotes G protein activation. Single channel recordings on VSMCs from wild-type and β1-knockout mice indicated that the presence of the regulatory β1 subunit was essential for the tungstate-mediated activation of BK channels in VSMCs. Moreover, the specific BK channel blocker iberiotoxin lowered tungstate-induced ERK phosphorylation by 55% and partially reverted (by 51%) the tungstate-produced reduction of platelet-derived growth factor (PDGF)-induced proliferation in human VSMCs. Our observations indicate that tungstate-targeting of BKαβ1 channels promotes activation of PTX-sensitive Gi proteins to enhance the tungstate-induced phosphorylation of ERK, and inhibits PDGF-stimulated cell proliferation in human vascular smooth muscle. PMID:25659150

  15. Infrared band intensities in ammonium hydroxide and ammonium salts

    NASA Technical Reports Server (NTRS)

    Sethna, P. P.; Downing, H. D.; Pinkley, L. W.; Williams, D.

    1978-01-01

    We have applied Kramers-Kronig analysis to reflection spectra to determine the optical constants of ammonium hydroxide and of aqueous solutions of ammonium chloride and bromide. From considerations of the absorption indices k(nu) we conclude that ammonium hydroxide consists of a solution of NH3 in water, in which NH3 molecules are hydrogen bonded to neighboring water molecules. The spectrum of ammonium hydroxide differs from the spectra of ammonium salts, in which bands characteristic of NH4(+) ions are prominent. The existence of ammonium hydroxide as an aerosol in planetary atmospheres is briefly discussed

  16. Amorphous tungstate precursor route to nanostructured tungsten oxide film with electrochromic property.

    PubMed

    Jeon, Ie-Rang; Kang, Joo-Hee; Paek, Seung-Min; Hwang, Seong-Ju; Choy, Jin-Ho

    2011-07-01

    Electrochromic tungsten oxide (WO3) films on ITO glass were fabricated by spin-coating with a tungsten peroxy acid solution, which was prepared by adding an equivolume mixture of hydrogen peroxide and glacial acetic acid to tungsten metal powder. The structural evolution of the tungstate precursor upon heat treatment was studied by X-ray diffraction (XRD) and X-ray absorption near edge structure (XANES) analyses, which indicated that the as-synthesized tungstate transformed into nanocrystalline WO3 upon heating. It is, therefore, quite clear that as-synthesized tungstate can be a good precursor for electrochromic WO3 films. A series of WO3 thin films were prepared on ITO glass by spin-coating with different concentrations of tungsten peroxy acid solution and then post-annealing at various temperatures. Depending on the concentration of the tungstate coating solution (200-500 mg mL(-1)) and the annealing temperature (100-300 degrees C), the thickness and WO3 content as well as the electrochromic properties of WO3 films can be controlled. As a result, the optimum fabrication conditions were determined to be a tungstate solution concentration of 300-400 mg mL(-1) and a post-annealing temperature of 200 degrees C. Finally, an inorganic-inorganic hybrid electrochromic device (ECD) composed of optimized WO3 and Prussian Blue (PB) with desirable coloration efficiency was successfully developed. PMID:22121748

  17. Synthesis and Characterization of Zirconium Tungstate Ultra-Thin Fibers

    SciTech Connect

    Zhang, Lifeng; Howe, Jane Y; Fong, Hao; Zhang, Yan

    2009-01-01

    This study reports an innovative method of electrospinning followed by pyrolysis to synthesize zirconium tungstate (ZrW2O8), a material with negative coefficient of thermal expansion (CTE), in ultra-thin fiber form. Morphologies and microstructures of the as-electrospun precursor fibers, the heat-treated intermediate fibers, and the final ZrW2O8 ultra-thin fibers were characterized by SEM, XRD, and TEM. The ZrW2O8 ultra-thin fibers had diameters in the sub-micrometer range with aspect ratios larger than 100; these fibers were polycrystalline, and consisted of single crystalline ZrW2O8 crystallites with sizes of 30-50 nm and surface roughness of several nanometers. The ZrW2O8 ultra-thin fibers are expected to outperform spherically, cylindrically, and/or irregularly shaped polycrystalline ZrW2O8 particles for the development of composites with precisely controlled CTEs. Additionally, this reported method could be utilized as a general approach to convert nano-scaled inorganic particles into fibers.

  18. Preclinical and Clinical Studies for Sodium Tungstate: Application in Humans

    PubMed Central

    Bertinat, Romina; Nualart, Francisco; Li, Xuhang; Yáñez, Alejandro J.; Gomis, Ramón

    2015-01-01

    Diabetes is a complex metabolic disorder triggered by the deficient secretion of insulin by the pancreatic β-cell or the resistance of peripheral tissues to the action of the hormone. Chronic hyperglycemia is the major consequence of this failure, and also the main cause of diabetic problems. Indeed, several clinical trials have agreed in that tight glycemic control is the best way to stop progression of the disease. Many anti-diabetic drugs for treatment of type 2 diabetes are commercially available, but no ideal normoglycemic agent has been developed yet. Moreover, weight gain is the most common side effect of many oral anti-diabetic agents and insulin, and increased weight has been shown to worsen glycemic control and increase the risk of diabetes progression. In this sense, the inorganic salt sodium tungstate (NaW) has been studied in different animal models of metabolic syndrome and diabetes, proving to have a potent effect on normalizing blood glucose levels and reducing body weight, without any hypoglycemic action. Although the liver has been studied as the main site of NaW action, positive effects have been also addressed in muscle, pancreas, brain, adipose tissue and intestine, explaining the effective anti-diabetic action of this salt. Here, we review NaW research to date in these different target organs. We believe that NaW deserves more attention, since all available anti-diabetic treatments remain suboptimal and new therapeutics are urgently needed. PMID:25995968

  19. 70. INTERIOR VIEW OF AMMONIUM NITRATE HOUSE, LOOKING AT AMMONIUM ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    70. INTERIOR VIEW OF AMMONIUM NITRATE HOUSE, LOOKING AT AMMONIUM NITRATE IN STORAGE. APRIL 18, 1919. - United States Nitrate Plant No. 2, Reservation Road, Muscle Shoals, Muscle Shoals, Colbert County, AL

  20. Glufosinate-ammonium

    Integrated Risk Information System (IRIS)

    Glufosinate - ammonium ; CASRN 77182 - 82 - 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 Noncarci

  1. The effects of tungstate on skin lesions caused by PPD in rats.

    PubMed

    Lee, Sang-Hee; Cho, Hyun-Gug; Lee, Sang-Il

    2008-04-01

    P-phenylenediamine (PPD) has been used as one of the ingredients in hair dye. The purpose of this study is to investigate the skin toxicity of PPD application in a tungstate-induced xanthine oxidase (XO) deficient animal model. PPD (2.5% PPD in 2% NH4OH) was applied to rat skin (25 mg/16.5 cm2) five times every other day in rats fed a standard diet (SD) or a tungstate supplemented diet (TD). The skin structure in the SD and the TD group was intact, whereas XO activity was not detected in the TD group during experimental periods. Furthermore, there were no differences between the SD and the TD group in dermal reactive oxygen species (ROS) scavenging enzymes. In these experimental conditions, although XO activity was not detected in the applied PPD rats fed a tungstate supplemented diet (PTD) group, it showed more severe tissue damage compared with the applied PPD rats fed a standard diet (PSD) group. In addition, the PTD group showed higher increased rates of ROS scavenging enzyme activity and lipid peroxide (LPO) content, and decreased glutathione (GSH) content than in the PSD group. In conclusion, the increase of PPD dermal toxicity in tungstate-induced XO deficient animals may be due to excessive ROS via ROS imbalance during PPD skin application. PMID:18379062

  2. Zirconium tungstate hydroxide hydrate revisited: Crystallization dependence on halide and hydronium ions

    SciTech Connect

    Colin, Julie A. Camper, DeMarco V.; Gates, Stacy D.; Simon, Monty D. Witker, Karen L. Lind, Cora

    2007-12-15

    The formation of zirconium tungstate hydroxide hydrate, a precursor to the negative thermal expansion material cubic zirconium tungstate, shows a strong dependence on hydrothermal reaction conditions. It was found that not only the acid concentration, but also the acid counterion plays a significant role in the crystallization of ZrW{sub 2}O{sub 7}(OH){sub 2}.2H{sub 2}O. High temperatures, high acid concentrations, and the presence of chloride or bromide ions promote the formation of well-crystallized ZrW{sub 2}O{sub 7}(OH){sub 2}.2H{sub 2}O. For low acid concentrations, a new zirconium tungstate hydrate polymorph is observed, which transforms to tetragonal ZrW{sub 2}O{sub 7}(OH){sub 2}.2H{sub 2}O at longer reaction times. A study of crystallization kinetics in hydrochloric acid is presented. - Graphical abstract: The formation of ZrW{sub 2}O{sub 7}(OH){sub 2}.2H{sub 2}O shows a strong dependence on reaction conditions. Both acid concentration and acid counterion play a significant role in the crystallization. High temperatures, high acid concentrations, and the presence of chloride or bromide ions promote the formation of well-crystallized ZrW{sub 2}O{sub 7}(OH){sub 2}.2H{sub 2}O. For low acid concentrations, a new zirconium tungstate hydrate polymorph is observed.

  3. Role of sodium tungstate as a potential antiplatelet agent

    PubMed Central

    Fernández-Ruiz, Rebeca; Pino, Marc; Hurtado, Begoña; García de Frutos, Pablo; Caballo, Carolina; Escolar, Ginés; Gomis, Ramón; Diaz-Ricart, Maribel

    2015-01-01

    Purpose Platelet inhibition is a key strategy in the management of atherothrombosis. However, the large variability in response to current strategies leads to the search for alternative inhibitors. The antiplatelet effect of the inorganic salt sodium tungstate (Na2O4W), a protein tyrosine phosphatase 1B (PTP1B) inhibitor, has been investigated in this study. Methods Wild-type (WT) and PTP1B knockout (PTP1B−/−) mice were treated for 1 week with Na2O4W to study platelet function with the platelet function analyzer PFA-100, a cone-and-plate analyzer, a flat perfusion chamber, and thrombus formation in vivo. Human blood aliquots were incubated with Na2O4W for 1 hour to measure platelet function using the PFA-100 and the annular perfusion chamber. Aggregometry and thromboelastometry were also performed. Results In WT mice, Na2O4W treatment prolonged closure times in the PFA-100 and decreased the surface covered (%SC) by platelets on collagen. Thrombi formed in a thrombosis mice model were smaller in animals treated with Na2O4W (4.6±0.7 mg vs 8.9±0.7 mg; P<0.001). Results with Na2O4W were similar to those in untreated PTP1B−/− mice (5.0±0.3 mg). Treatment of the PTP1B−/− mice with Na2O4W modified only slightly this response. In human blood, a dose-dependent effect was observed. At 200 μM, closure times in the PFA-100 were prolonged. On denuded vessels, %SC and thrombi formation (%T) decreased with Na2O4W. Neither the aggregating response nor the viscoelastic clot properties were affected. Conclusion Na2O4W decreases consistently the hemostatic capacity of platelets, inhibiting their adhesive and cohesive properties under flow conditions in mice and in human blood, resulting in smaller thrombi. Although Na2O4W may be acting on platelet PTP1B, other potential targets should not be disregarded. PMID:26060394

  4. New family of tungstate-responsive transcriptional regulators in sulfate-reducing bacteria.

    PubMed

    Kazakov, Alexey E; Rajeev, Lara; Luning, Eric G; Zane, Grant M; Siddartha, Kavya; Rodionov, Dmitry A; Dubchak, Inna; Arkin, Adam P; Wall, Judy D; Mukhopadhyay, Aindrila; Novichkov, Pavel S

    2013-10-01

    The trace elements molybdenum and tungsten are essential components of cofactors of many metalloenzymes. However, in sulfate-reducing bacteria, high concentrations of molybdate and tungstate oxyanions inhibit growth, thus requiring the tight regulation of their homeostasis. By a combination of bioinformatic and experimental techniques, we identified a novel regulator family, tungstate-responsive regulator (TunR), controlling the homeostasis of tungstate and molybdate in sulfate-reducing deltaproteobacteria. The effector-sensing domains of these regulators are similar to those of the known molybdate-responsive regulator ModE, while their DNA-binding domains are homologous to XerC/XerD site-specific recombinases. Using a comparative genomics approach, we identified DNA motifs and reconstructed regulons for 40 TunR family members. Positional analysis of TunR sites and putative promoters allowed us to classify most TunR proteins into two groups: (i) activators of modABC genes encoding a high-affinity molybdenum and tungsten transporting system and (ii) repressors of genes for toluene sulfonate uptake (TSUP) family transporters. The activation of modA and modBC genes by TunR in Desulfovibrio vulgaris Hildenborough was confirmed in vivo, and we discovered that the activation was diminished in the presence of tungstate. A predicted 30-bp TunR-binding motif was confirmed by in vitro binding assays. A novel TunR family of bacterial transcriptional factors controls tungstate and molybdate homeostasis in sulfate-reducing deltaproteobacteria. We proposed that TunR proteins participate in protection of the cells from the inhibition by these oxyanions. To our knowledge, this is a unique case of a family of bacterial transcriptional factors evolved from site-specific recombinases. PMID:23913324

  5. Hydrothermal synthesis of ammonium illite

    USGS Publications Warehouse

    Sucha, V.; Elsass, F.; Eberl, D.D.; Kuchta, L'.; Madejova, J.; Gates, W.P.; Komadel, P.

    1998-01-01

    Synthetic gel and glass of illitic composition, natural kaolinite, and mixed-layer illite-smectite were used as starting materials for hydrothermal synthesis of ammonium illite. Ammonium illite was prepared from synthetic gel by hydrothermal treatment at 300??C. The onset of crystallization began within 3 h, and well-crystallized ammonium illite appeared at 24 h. Increasing reaction time (up to four weeks) led to many illite layers per crystal. In the presence of equivalent proportions of potassium and ammonium, the gel was transformed to illite with equimolar contents of K and NH4. In contrast, synthesis using glass under the same conditions resulted in a mixture of mixed-layer ammonium illite-smectite with large expandability and discrete illite. Hydrothermal treatments of the fine fractions of natural kaolinite and illite-smectite produced ammonium illite from kaolinite but the illite-smectite remained unchanged.

  6. Time- and energy-efficient solution combustion synthesis of binary metal tungstate nanoparticles with enhanced photocatalytic activity.

    PubMed

    Thomas, Abegayl; Janáky, Csaba; Samu, Gergely F; Huda, Muhammad N; Sarker, Pranab; Liu, J Ping; van Nguyen, Vuong; Wang, Evelyn H; Schug, Kevin A; Rajeshwar, Krishnan

    2015-05-22

    In the search for stable and efficient photocatalysts beyond TiO2 , the tungsten-based oxide semiconductors silver tungstate (Ag2 WO4 ), copper tungstate (CuWO4 ), and zinc tungstate (ZnWO4 ) were prepared using solution combustion synthesis (SCS). The tungsten precursor's influence on the product was of particular relevance to this study, and the most significant effects are highlighted. Each sample's photocatalytic activity towards methyl orange degradation was studied and benchmarked against their respective commercial oxide sample obtained by solid-state ceramic synthesis. Based on the results herein, we conclude that SCS is a time- and energy-efficient method to synthesize crystalline binary tungstate nanomaterials even without additional excessive heat treatment. As many of these photocatalysts possess excellent photocatalytic activity, the discussed synthetic strategy may open sustainable materials chemistry avenues to solar energy conversion and environmental remediation. PMID:26018624

  7. Ammonium diphosphitoindate(III)

    PubMed Central

    Hamchaoui, Farida; Rebbah, Houria; Le Fur, Eric

    2013-01-01

    The crystal structure of the title compound, NH4[In(HPO3)2], is built up from InIII cations (site symmetry 3m.) adopting an octa­hedral environment and two different phosphite anions (each with site symmetry 3m.) exhibiting a triangular–pyramidal geometry. Each InO6 octa­hedron shares its six apices with hydrogen phosphite groups. Reciprocally, each HPO3 group shares all its O atoms with three different metal cations, leading to [In(HPO3)2]− layers which propagate in the ab plane. The ammonium cation likewise has site symmetry 3m.. In the structure, the cations are located between the [In(HPO3)2]− layers of the host framework. The sheets are held together by hydrogen bonds formed between the NH4 + cations and the O atoms of the framework. PMID:23633983

  8. Ammonium diphosphitoindate(III).

    PubMed

    Hamchaoui, Farida; Rebbah, Houria; Le Fur, Eric

    2013-04-01

    The crystal structure of the title compound, NH4[In(HPO3)2], is built up from In(III) cations (site symmetry 3m.) adopting an octa-hedral environment and two different phosphite anions (each with site symmetry 3m.) exhibiting a triangular-pyramidal geometry. Each InO6 octa-hedron shares its six apices with hydrogen phosphite groups. Reciprocally, each HPO3 group shares all its O atoms with three different metal cations, leading to [In(HPO3)2](-) layers which propagate in the ab plane. The ammonium cation likewise has site symmetry 3m.. In the structure, the cations are located between the [In(HPO3)2](-) layers of the host framework. The sheets are held together by hydrogen bonds formed between the NH4 (+) cations and the O atoms of the framework. PMID:23633983

  9. Oral tungstate (Na2WO4) exposure reduces adaptive immune responses in mice after challenge.

    PubMed

    Osterburg, Andrew R; Robinson, Chad T; Mokashi, Vishwesh; Stockelman, Michael; Schwemberger, Sandy J; Chapman, Gail; Babcock, George F

    2014-01-01

    Tungstate (WO²⁻₄) has been identified as a ground water contaminant at military firing ranges and can be absorbed by ingestion. In this study, C57BL6 mice were exposed to sodium tungstate (Na2WO4·2H2O) (0, 2, 62.5, 125, and 200 mg/kg/day) in their drinking water for an initial 28-day screen and in a one-generation (one-gen) model. Twenty-four hours prior to euthanasia, mice were intraperitoneally injected with Staphylococcal enterotoxin B (SEB) (20 μg/mouse) or saline as controls. After euthanasia, splenocytes and blood were collected and stained with lymphocyte and/or myeloid immunophenotyping panels and analyzed by flow cytometry. In the 28-day and one-gen exposure, statistically significant reductions were observed in the quantities of activated cytotoxic T-cells (TCTL; CD3(+)CD8(+)CD71(+)) and helper T-cells (TH; CD3(+)CD4(+)CD71(+)) from spleens of SEB-treated mice. In the 28-day exposures, CD71(+) TCTL cells were 12.87 ± 2.05% (SE) in the 0 tungstate (control) group compared to 4.44 ± 1.42% in the 200 mg/kg/day (p < 0.001) group. TH cells were 4.85 ± 1.23% in controls and 2.76 ± 0.51% in the 200 mg/kg/day (p < 0.003) group. In the one-gen exposures, TCTL cells were 7.98 ± 0.49% and 6.33 ± 0.49% for P and F1 mice after 0 mg/kg/day tungstate vs 1.58 ± 0.23% and 2.52 ± 0.25% after 200 mg/kg/day of tungstate (p < 0.001). Similarly, TH cells were reduced to 6.21 ± 0.39% and 7.20 ± 0.76%, respectively, for the 0 mg/kg/day P and F1 mice, and 2.28 ± 0.41% and 2.85 ± 0.53%, respectively, for the 200 mg/kg/day tungstate P and F1 groups (p < 0.001). In delayed-type hypersensitivity Type IV experiments, tungstate exposure prior to primary and secondary antigen challenge significantly reduced footpad swelling at 20 and 200 mg/kg/day. These data indicate that exposure to tungstate can result in immune suppression that may, in turn, reduce host defense against

  10. High power tungstate-crystal Raman laser operating in the strong thermal lensing regime.

    PubMed

    McKay, Aaron; Kitzler, Ondrej; Mildren, Richard P

    2014-01-13

    We report an investigation into a double metal tungstate Raman laser when pumped at elevated average powers. Potassium gadolinium tungstate (KGW) was placed in an external cavity configured for second-Stokes output and pumped at pulse repetition rate of 38 kHz with up to 46 W of average power. For output powers above 3 W, we observe preferential excitation of Hermite-Gaussian transverse modes whose order in the X(1)(') principal direction of the thermal expansion tensor scales linearly with Raman power. We deduce that strong astigmatic thermal lensing is induced in the Raman crystal with a negative component in the X(1)(') direction. At maximum pump power, 8.3 W of output power was obtained at a conversion efficiency of 18%. PMID:24515030

  11. Distribution of tungstate in pregnant mice and effects on embryonic cells in vitro

    SciTech Connect

    Wide, M.; Danielsson, B.R.G.; Dencker, L.

    1986-08-01

    Whole-body autoradiography and impulse counting experiments were used to study the distribution and retention of radioactivity in the pregnant mouse after administration of (/sup 185/W)tungstate. A rapid uptake was found in a number of tissues - skeleton, red pulp of the spleen, adrenal, liver, thyroid, pituitary, and ovary - and in the intestine and kidneys, through which it was rapidly excreted. /sup 185/W was also readily transported from mother to fetus, although more in late than in early gestation. The largest metal retention was found in the maternal skeleton, kidneys, and spleen and in visceral yolk sac epithelium and the skeleton of the fetus. Furthermore, in vitro cytotoxicity experiments showed inhibition by tungstate of cartilage production in limb bud mesenchymal cultures at concentrations similar to those found in vivo.

  12. Separation of Molybdenum from Tungstate Solution—Scavenging Thiomolybdate by Copper Compound

    NASA Astrophysics Data System (ADS)

    Zhao, Zhongwei; Gao, Lili; Cao, Caifang; Li, Jiangtao; Chen, Xingyu; Chen, Ailiang; Liu, Xuheng; Sun, Peimei; Huo, Guangsheng; Li, Yunjiao; Li, Honggui

    2012-12-01

    Molybdenum is frequently associated with tungsten in mineral deposits, and their chemical properties are quite similar. Therefore, for many years, removal of impurity molybdenum from tungsten has been a worldwide technical problem. In this work, a separation process was investigated with the use of copper-bearing materials as the scavenging agents. Various conditions involved in the effects of different copper-bearing materials, dosage of scavenging agents, reaction time, and temperature were studied in detail. It was found that thiomolybdate can be selectively precipitated from tungstate solution by all the scavenging agents, especially when using nascent copper sulfide. Removal of thiomlybdate can reach 99.45 pct under optimum condition. Nascent CuS is an economic and efficient reagent for removing Mo from tungstate solution.

  13. Crucibleless crystal growth and Radioluminescence study of calcium tungstate single crystal fiber

    NASA Astrophysics Data System (ADS)

    Silva, M. S.; Jesus, L. M.; Barbosa, L. B.; Ardila, D. R.; Andreeta, J. P.; Silva, R. S.

    2014-11-01

    In this article, single phase and high optical quality scheelite calcium tungstate single crystal fibers were grown by using the crucibleless laser heated pedestal growth technique. The as-synthesized calcium tungstate powders used for shaping seed and feed rods were investigated by X-ray diffraction technique. As-grown crystals were studied by Raman spectroscopy and Radioluminescence measurements. The results indicate that in both two cases, calcined powder and single crystal fiber, only the expected scheelite CaWO4 phase was observed. It was verified large homogeneity in the crystal composition, without the presence of secondary phases. The Radioluminescence spectra of the as-grown single crystal fibers are in agreement with that present in Literature for bulk single crystals, presented a single emission band centered at 420 nm when irradiated with β-rays.

  14. MOF-Derived Tungstated Zirconia as Strong Solid Acids toward High Catalytic Performance for Acetalization.

    PubMed

    Wang, Peng; Feng, Jian; Zhao, Yupei; Wang, Shaobin; Liu, Jian

    2016-09-14

    A strong solid acid, tungstated zirconia (WZ), has been prepared first using tungstate immobilized UiO-66 as precursors through a "double-solvent" impregnation method under mild calcination temperature. With moderate W contents, the as-synthesized WZ catalysts possess a high density of acid sites, and the proper heat treatment also has facilely led to a bunch of oligomeric tungsten clusters on stabilized tetragonal ZrO2. The resultant solid acids show an improved catalytic performance toward the benzaldehyde's acetalization in comparison with traditional zirconium hydroxide-prepared WZ. Notably, due to large surface area and additionally introduced strong acid sites, the MOF-derived WZ catalysts afforded conversion up to 86.0%. The facile method endows the WZ catalysts with superior catalytic activities and excellent recyclability, thus opening a new avenue for preparation of metal oxide-based solid superacids and superbases. PMID:27557351

  15. One-step synthesis and luminescence properties of tetragonal double tungstates nanocrystals.

    PubMed

    Wang, Z J; Zhang, Y L; Zhong, J P; Yao, H H; Wang, J; Wu, M M; Meijerink, A

    2016-08-25

    A versatile one-step thermolysis protocol is demonstrated to produce a uniform dispersion of tetragonal double tungstates NaRE(WO4)2 (RE = rare earth) nanocrystals (NCs). Oriented attachment in the [001] direction occurred. Doping with luminescent RE(3+) ions resulted in highly luminescent NCs showing characteristic line emission of the dopant as well as a blue emission assigned to surface adsorbed organic species. PMID:27524472

  16. A photon calorimeter using lead tungstate crystals for the CEBAF HAll A Compton polarimeter

    SciTech Connect

    D. Neyret; T. Pussieux; T. Auger; M. Baylac; E. Burtin; C. Cavata; R. Chipaux; S. Escoffier; N. Falletto; J. Jardillier; S. Kerhoas; D. Lhuillier; F. Marie; C. Veyssiere; J. Ahrens; R. Beck; M. Lang

    2000-05-01

    A new Compton polarimeter is built on the CEBAF Hall A electron beam line. Performances of 10% resolution and 1% calibration are required for the photon calorimeter of this polarimeter. This calorimeter is built with lead tungstate scintillators coming from the CMS electromagnetic calorimeter R&D. Beam tests of this detector have been made using the tagged photon beam line at MAMI, Mainz, and a resolution of 1.76%+2.75%/v+0.41%/E has been measured.

  17. Tungstate decreases weight gain and adiposity in obese rats through increased thermogenesis and lipid oxidation.

    PubMed

    Claret, Marc; Corominola, Helena; Canals, Ignasi; Saura, Josep; Barcelo-Batllori, Silvia; Guinovart, Joan J; Gomis, Ramon

    2005-10-01

    The increasing worldwide incidence of obesity and the limitations of current treatments raise the need for finding novel therapeutic approaches to treat this disease. The purpose of the current study was first to investigate the effects of tungstate on body weight and insulin sensitivity in a rat model of diet-induced obesity. Second, we aimed to gain insight into the molecular mechanisms underlying its action. Oral administration of tungstate significantly decreased body weight gain and adiposity without modifying caloric intake, intestinal fat absorption, or growth rate in obese rats. Moreover, the treatment ameliorated dislipemia and insulin resistance of obese rats. These effects were mediated by an increase in whole-body energy dissipation and by changes in the expression of genes involved in the oxidation of fatty acids and mitochondrial uncoupling in adipose tissue. Furthermore, treatment increased the number of small adipocytes with a concomitant induction of apoptosis. Our results indicate that tungstate treatment may provide the basis for a promising novel therapy for obesity. PMID:16002523

  18. Tungstate, a Molybdate Analog Inactivating Nitrate Reductase, Deregulates the Expression of the Nitrate Reductase Structural Gene

    PubMed Central

    Deng, Mingde; Moureaux, Thérèse; Caboche, Michel

    1989-01-01

    Nitrate reductase (NR, EC 1.6.6.1) from higher plants is a homodimeric enzyme carrying a molybdenum cofactor at the catalytic site. Tungsten can be substituted for molybdenum in the cofactor structure, resulting in an inactive enzyme. When nitratefed Nicotiana tabacum plants were grown on a nutrient solution in which tungstate was substituted for molybdate, NR activity in the leaves decreased to a very low level within 24 hours while NR protein accumulated progressively to a level severalfold higher than the control after 6 days. NR mRNA level in molybdate-grown plants exhibited a considerable day-night fluctuation. However, when plants were treated with tungstate, NR mRNA level remained very high. NR activity and protein increased over a 24-hour period when nitrate was added back to N-starved molybdate-grown plants. NR mRNA level increased markedly during the first 2 hours and then decreased. In the presence of tungstate, however, the induction of NR activity by nitrate was totally abolished while high levels of NR protein and mRNA were both induced, and the high level of NR mRNA was maintained over a 10-hour period. These results suggest that the substitution of tungsten for molybdenum in NR complex leads to an overexpression of the NR structural gene. Possible mechanisms involved in this deregulation are discussed. Images Figure 2 Figure 3 Figure 5 PMID:16667015

  19. THE EFFECT OF TUNGSTATE NANOPARTICLES ON REACTIVE OXYGEN SPECIES AND CYTOTOXICITY IN RAW 264.7 MOUSE MONOCYTE MACROPHAGE CELLS

    PubMed Central

    Dunnick, Katherine M.; Badding, Melissa A.; Schwegler-Berry, Diane; Patete, Jonathan M.; Koenigsmann, Christopher; Wong, Stanislaus S.; Leonard, Stephen S.

    2015-01-01

    Due to their unique size, surface area, and chemical characteristics, nanoparticles’ use in consumer products has increased. However, the toxicity of nanoparticle (NP) exposure during the manufacturing process has not been fully assessed. Tungstate NP are used in numerous products, including but not limited to scintillator detectors and fluorescent lighting. As with many NP, no apparent toxicity studies have been completed with tungstate NP. The hypothesis that tungstate NP in vitro exposure results in reactive oxygen species (ROS) formation and cytotoxicity was examined. Differences in toxicity based on tungstate NP size, shape (sphere vs. wire), and chemical characteristics were determined. RAW 264.7 mouse monocyte macrophages were exposed to tungstate NP, and ROS formation was assessed via electron spin resonance (ESR), and several assays including hydrogen peroxide, intracellular ROS, and Comet. Results showed ROS production induced by tungstate nanowire exposure, but this exposure did not result in oxidative DNA damage. Nanospheres showed neither ROS nor DNA damage following cellular exposure. Cells were exposed over 72 h to assess cytotoxicity using an MTT (tetrazolium compound) assay. Results showed that differences in cell death between wires and spheres occurred at 24 h but were minimal at both 48 and 72 h. The present results indicate that tungstate nanowires are more reactive and produce cell death within 24 h of exposure, whereas nanospheres are less reactive and did not produce cell death. Results suggest that differences in shape may affect reactivity. However, regardless of the differences in reactivity, in general both shapes produced mild ROS and resulted in minimal cell death at 48 and 72 h in RAW 264.7 cells. PMID:25208664

  20. A quantitative study of sodium tungstate protective effect on pancreatic beta cells in streptozotocin-induced diabetic rats.

    PubMed

    Heidari, Zahra; Mahmoudzadeh-Sagheb, Hamidreza; Moudi, Bita

    2008-12-01

    Diabetes is a major public health problem. Development of new therapies that are able to improve glycemia management, cure diabetes, and can even protect from it, are of great interest. This study investigated the protective effect of sodium tungstate against STZ-induced beta-cell damages by means of stereological methods. Sixty rats were divided into six groups: control (C), tungstate-treated control (TC), STZ-induced diabetic (D), STZ-induced diabetic rats were treated by sodium tungstate from 1 week before STZ injection (TDB), food-restricted diabetic (FRD), and diabetic rats treated with sodium tungstate 1 week after STZ administration (TDA). Stereological estimation of pancreas volume, islets volume density, volume-weighted mean islets volume and mass of beta cells, islets, and pancreas and total number of islets were done. Islets volume density, volume-weighted mean islets volume, and mass of beta cells, islets, and pancreas of TDB group was significantly higher than D, FRD and TDA groups (P<0.001) and was comparable to controls (C and TC groups). Total number of islets, pancreas wet weight and volume did not show any significant changes between these groups (P>0.05). Results suggested that sodium tungstate preserves pancreatic beta cells from STZ-induced damages and diabetes induction in rats. PMID:18400503

  1. Efficacy of some antioxidants supplementation in reducing oxidative stress post sodium tungstate exposure in male wistar rats.

    PubMed

    Sachdeva, S; Flora, S J S

    2014-04-01

    This study aimed to evaluate the protective efficacy of some antioxidants against sodium tungstate induced oxidative stress in male wistar rats. Animals were sub-chronically exposed to sodium tungstate (100ppm in drinking water) for three months except for control group. In the same time, many rats were supplemented orally with different antioxidants (alpha-lipoic acid (ALA), n-acetylcysteine (NAC), quercetin or naringenin (0.30mM)) for five consecutive days a week for the same mentioned period before. Exposure to sodium tungstate significantly (P<0.05) inhibit blood δ-aminolevulinic acid dehydratase (ALAD) activity, liver and blood reduced glutathione (GSH) levels and an increase in oxidized glutathione (GSSG) and thiobarbituric acid reactive species (TBARS) levels in tissues. ALA acid and NAC supplementation post sodium tungstate exposure increased GSH and also, was beneficial in the recovery of altered superoxide dismutase and catalase activity, besides, significantly reducing blood and tissue reactive oxygen species and TBARS levels. The results suggest a more pronounced efficacy of ALA acid and NAC supplementation than quercetin or naringenin supplementation post sodium tungstate exposure in preventing induced oxidative stress in rats. PMID:24613855

  2. High performance ammonium nitrate propellant

    NASA Technical Reports Server (NTRS)

    Anderson, F. A. (Inventor)

    1979-01-01

    A high performance propellant having greatly reduced hydrogen chloride emission is presented. It is comprised of: (1) a minor amount of hydrocarbon binder (10-15%), (2) at least 85% solids including ammonium nitrate as the primary oxidizer (about 40% to 70%), (3) a significant amount (5-25%) powdered metal fuel, such as aluminum, (4) a small amount (5-25%) of ammonium perchlorate as a supplementary oxidizer, and (5) optionally a small amount (0-20%) of a nitramine.

  3. 21 CFR 184.1138 - Ammonium chloride.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... GRAS § 184.1138 Ammonium chloride. (a) Ammonium chloride (NH4Cl, CAS Reg. No. 12125-02-9) is produced by the reaction of sodium chloride and an ammonium salt in solution. The less soluble sodium salt... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ammonium chloride. 184.1138 Section 184.1138...

  4. 21 CFR 184.1143 - Ammonium sulfate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ammonium sulfate. 184.1143 Section 184.1143 Food... Specific Substances Affirmed as GRAS § 184.1143 Ammonium sulfate. (a) Ammonium sulfate ((NH4)2SO4, CAS Reg... is prepared by the neutralization of sulfuric acid with ammonium hydroxide. (b) The ingredient...

  5. 21 CFR 184.1137 - Ammonium carbonate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...). It is prepared by the sublimation of a mixture of ammonium sulfate and calcium carbonate and occurs... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ammonium carbonate. 184.1137 Section 184.1137 Food... Specific Substances Affirmed as GRAS § 184.1137 Ammonium carbonate. (a) Ammonium carbonate ((NH4)2CO3,...

  6. 21 CFR 184.1143 - Ammonium sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ammonium sulfate. 184.1143 Section 184.1143 Food... GRAS § 184.1143 Ammonium sulfate. (a) Ammonium sulfate ((NH4)2SO4, CAS Reg. No. 7783-20-2) occurs... neutralization of sulfuric acid with ammonium hydroxide. (b) The ingredient meets the specifications of the...

  7. 21 CFR 184.1143 - Ammonium sulfate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ammonium sulfate. 184.1143 Section 184.1143 Food... Specific Substances Affirmed as GRAS § 184.1143 Ammonium sulfate. (a) Ammonium sulfate ((NH4)2SO4, CAS Reg... is prepared by the neutralization of sulfuric acid with ammonium hydroxide. (b) The ingredient...

  8. 21 CFR 184.1137 - Ammonium carbonate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...). It is prepared by the sublimation of a mixture of ammonium sulfate and calcium carbonate and occurs... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ammonium carbonate. 184.1137 Section 184.1137 Food... Specific Substances Affirmed as GRAS § 184.1137 Ammonium carbonate. (a) Ammonium carbonate ((NH4)2CO3,...

  9. Precision machining, polishing and measurement of mechanical and toxicological properties of lead tungstate crystals for the CMS electromagnetic calorimeter

    SciTech Connect

    Wuest, C.R.; Fuchs, B.A.; Shi, X.

    1995-08-01

    We have developed new machining and polishing techniques that have previously been applied to large scintillating crystal arrays for high energy physics experiments such as the Barium Fluoride Electromagnetic Calorimeter for the GEM Detector at SSCL, the LCsI Electromagnetic Calorimeter for the BaBar Detector at PEP-II B Factory at SLAC and the 110,000 crystal CMS Lead Tungstate Electromagnetic Calorimeter at LHC at CERN. We discuss earlier results achieved with diamond machining and polishing methods and present new results on diamond machining of lead tungstate crystals. Additionally we present new results on mechanical properties of lead tungstate including toxicological data important for the safe handling and processing of this material.

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

    PubMed

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

    2016-08-18

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

  11. 46 CFR 148.205 - Ammonium nitrate and ammonium nitrate fertilizers.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 46 Shipping 5 2011-10-01 2011-10-01 false Ammonium nitrate and ammonium nitrate fertilizers. 148... Materials § 148.205 Ammonium nitrate and ammonium nitrate fertilizers. (a) This section applies to the stowage and transportation in bulk of ammonium nitrate and the following fertilizers composed of...

  12. 46 CFR 148.205 - Ammonium nitrate and ammonium nitrate fertilizers.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 46 Shipping 5 2014-10-01 2014-10-01 false Ammonium nitrate and ammonium nitrate fertilizers. 148... Materials § 148.205 Ammonium nitrate and ammonium nitrate fertilizers. (a) This section applies to the stowage and transportation in bulk of ammonium nitrate and the following fertilizers composed of...

  13. 46 CFR 148.205 - Ammonium nitrate and ammonium nitrate fertilizers.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 46 Shipping 5 2013-10-01 2013-10-01 false Ammonium nitrate and ammonium nitrate fertilizers. 148... Materials § 148.205 Ammonium nitrate and ammonium nitrate fertilizers. (a) This section applies to the stowage and transportation in bulk of ammonium nitrate and the following fertilizers composed of...

  14. 46 CFR 148.205 - Ammonium nitrate and ammonium nitrate fertilizers.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 46 Shipping 5 2012-10-01 2012-10-01 false Ammonium nitrate and ammonium nitrate fertilizers. 148... Materials § 148.205 Ammonium nitrate and ammonium nitrate fertilizers. (a) This section applies to the stowage and transportation in bulk of ammonium nitrate and the following fertilizers composed of...

  15. TupA: A Tungstate Binding Protein in the Periplasm of Desulfovibrio alaskensis G20

    PubMed Central

    Otrelo-Cardoso, Ana Rita; Nair, Rashmi R.; Correia, Márcia A. S.; Rivas, Maria G.; Santos-Silva, Teresa

    2014-01-01

    The TupABC system is involved in the cellular uptake of tungsten and belongs to the ABC (ATP binding cassette)-type transporter systems. The TupA component is a periplasmic protein that binds tungstate anions, which are then transported through the membrane by the TupB component using ATP hydrolysis as the energy source (the reaction catalyzed by the ModC component). We report the heterologous expression, purification, determination of affinity binding constants and crystallization of the Desulfovibrio alaskensis G20 TupA. The tupA gene (locus tag Dde_0234) was cloned in the pET46 Enterokinase/Ligation-Independent Cloning (LIC) expression vector, and the construct was used to transform BL21 (DE3) cells. TupA expression and purification were optimized to a final yield of 10 mg of soluble pure protein per liter of culture medium. Native polyacrylamide gel electrophoresis was carried out showing that TupA binds both tungstate and molybdate ions and has no significant interaction with sulfate, phosphate or perchlorate. Quantitative analysis of metal binding by isothermal titration calorimetry was in agreement with these results, but in addition, shows that TupA has higher affinity to tungstate than molybdate. The protein crystallizes in the presence of 30% (w/v) polyethylene glycol 3350 using the hanging-drop vapor diffusion method. The crystals diffract X-rays beyond 1.4 Å resolution and belong to the P21 space group, with cell parameters a = 52.25 Å, b = 42.50 Å, c = 54.71 Å, β = 95.43°. A molecular replacement solution was found, and the structure is currently under refinement. PMID:24992597

  16. Effect of thermal annealing on the phase evolution of silver tungstate in Ag/WO₃ films.

    PubMed

    Bose, R Jolly; Sreedharan, R Sreeja; Krishnan, R Resmi; Reddy, V R; Gupta, Mukul; Ganesan, V; Sudheer, S K; Pillai, V P Mahadevan

    2015-06-15

    Silver/tungsten oxide multi-layer films are deposited over quartz substrates by RF magnetron sputtering technique and the films are annealed at temperatures 200, 400 and 600°C. The effect of thermal annealing on the phase evolution of silver tungstate phase in Ag/WO3 films is studied extensively using techniques like X-ray diffraction, micro-Raman analysis, atomic force microscopy and photoluminescence studies. The XRD pattern of the as-deposited film shows only the peaks of cubic phase of silver. The film annealed at 200°C shows the presence of XRD peaks corresponding to orthorhombic phase of Ag2WO4 and peaks corresponding to cubic phase of silver with reduced intensity. It is found that, as annealing temperature increases, the volume fraction of Ag decreases and that of Ag2WO4 phase increases and becomes highest at a temperature of 400°C. When the temperature increases beyond 400°C, the volume fraction of Ag2WO4 decreases, due to its decomposition into silver and oxygen deficient phase Ag2W4O13. The micro-Raman spectra of the annealed films show the characteristic bands of tungstate phase which is in agreement with XRD analysis. The surface morphology of the films studied by atomic force microscopy reveals that the particle size and r.m.s roughness are highest for the sample annealed at 400°C. In the photoluminescence study, the films with silver tungstate phase show an emission peak in blue region centered around the wavelength 441 nm (excitation wavelength 256 nm). PMID:25791880

  17. Anaerobic ammonium oxidation for treatment of ammonium-rich wastewaters*

    PubMed Central

    Zhang, Lei; Zheng, Ping; Tang, Chong-jian; Jin, Ren-cun

    2008-01-01

    The concept of anaerobic ammonium oxidation (ANAMMOX) is presently of great interest. The functional bacteria belonging to the Planctomycete phylum and their metabolism are investigated by microbiologists. Meanwhile, the ANAMMOX is equally valuable in treatment of ammonium-rich wastewaters. Related processes including partial nitritation-ANAMMOX and completely autotrophic nitrogen removal over nitrite (CANON) have been developed, and lab-scale experiments proved that both processes were quite feasible in engineering with appropriate control. Successful full-scale practice in the Netherlands will accelerate application of the process in future. This review introduces the microbiology and more focuses on application of the ANAMMOX process. PMID:18500782

  18. Comparative DFT study of crystalline ammonium perchlorate and ammonium dinitramide.

    PubMed

    Zhu, Weihua; Wei, Tao; Zhu, Wei; Xiao, Heming

    2008-05-22

    The electronic structure, vibrational properties, absorption spectra, and thermodynamic properties of crystalline ammonium perchlorate (AP) and ammonium dinitramide (ADN) have been comparatively studied using density functional theory in the local density approximation. The results shows that the p states for the two solids play a very important role in their chemical reaction. From the low frequency to high frequency region, ADN has more motion modes for the vibrational frequencies than AP. The absorption spectra of AP and ADN display a few, strong bands in the fundamental absorption region. The thermodynamic properties show that ADN is easier to decompose than AP as the temperature increases. PMID:18396853

  19. TREATMENT OF AMMONIUM NITRATE SOLUTIONS

    DOEpatents

    Boyer, T.W.; MacHutchin, J.G.; Yaffe, L.

    1958-06-10

    The treatment of waste solutions obtained in the processing of neutron- irradiated uranium containing fission products and ammonium nitrate is described. The object of this process is to provide a method whereby the ammonium nitrate is destroyed and removed from the solution so as to permit subsequent concentration of the solution.. In accordance with the process the residual nitrate solutions are treated with an excess of alkyl acid anhydride, such as acetic anhydride. Preferably, the residual nitrate solution is added to an excess of the acetic anhydride at such a rate that external heat is not required. The result of this operation is that the ammonium nitrate and acetic anhydride react to form N/sub 2/ O and acetic acid.

  20. Deposition of Highly Luminescent Zinc Tungstate Thin Films on Various Substrates

    NASA Astrophysics Data System (ADS)

    Farrakhan, Rashad

    Zinc tungstate films have promising applications in small form factor backscatter electron detectors. We are developing a multistep technology for synthesis of these films. Zinc and tungsten were co-sputtered onto substrates through the process of magnetron sputtering. The metallic films were oxidized in a vacuum sealed tube furnace in controlled flow of argon and oxygen at 800 °C. The chemical composition of the film was characterized by Energy-Dispersive X-Ray Spectroscopy (EDS). The structure of the film was investigated by Raman Spectroscopy. The photoluminescence quantum efficiency of the films was found to be 60%. Process parameters for obtaining the desired 1-1 ratio of zinc to tungsten in the film is explored through varying factors such as: the composition of the target used in the sputtering, the power and or voltage used in the sputtering process. Our experiments show that zinc tungstate thin films can be deposited on various substrates with good adhesion and mechanical integrity, and still be efficient light emitters.

  1. Double aberration-corrected TEM/STEM of tungstated zirconia nanocatalysts for the synthesis of paracetamol

    NASA Astrophysics Data System (ADS)

    Yoshida, K.; Shiju, N. R.; Brown, D. R.; Boyes, E. D.; Gai, P. L.

    2010-07-01

    We report highly active tungstated zirconia nanocatalysts for the synthesis of paracetamol by Beckmann rearrangement of 4-hydroxyacetophenone oxime. Double aberration-corrected (2AC)-TEM/STEM studies were performed in a JEOL 2200FS FEG TEM/STEM at the 1 Angstrom (1 Å = 0.1 nanometer) level. Observations at close to zero defocus were carried out using the AC-TEM as well as AC-STEM including high angle annular dark field (HAADF) imaging, from the same areas of the catalyst crystallites. The studies from the same areas have revealed the location and the nanostructure of the polytungstate species (clusters) and the nanograins of zirconia. The AC (S)TEM was crucial to observe the nanostructure and location of polytungstate clusters on the zirconia grains. Polytungstate clusters as small as 0.5 nm have been identified using the HAADF-STEM. The nanostructures of the catalyst and the W surface density have been correlated with paracetamol reaction studies. The results demonstrate the nature of active sites and high activity of the tungstated zirconia nanocatalyst, which is an environmentally clean alternative to the current homogeneous process.

  2. Two-Dimensional Iron Tungstate: A Ternary Oxide Layer With Honeycomb Geometry

    PubMed Central

    2016-01-01

    The exceptional physical properties of graphene have sparked tremendous interests toward two-dimensional (2D) materials with honeycomb structure. We report here the successful fabrication of 2D iron tungstate (FeWOx) layers with honeycomb geometry on a Pt(111) surface, using the solid-state reaction of (WO3)3 clusters with a FeO(111) monolayer on Pt(111). The formation process and the atomic structure of two commensurate FeWOx phases, with (2 × 2) and (6 × 6) periodicities, have been characterized experimentally by combination of scanning tunneling microscopy (STM), low-energy electron diffraction (LEED), X-ray photoelectron spectroscopy (XPS), and temperature-programmed desorption (TPD) and understood theoretically by density functional theory (DFT) modeling. The thermodynamically most stable (2 × 2) phase has a formal FeWO3 stoichiometry and corresponds to a buckled Fe2+/W4+ layer arranged in a honeycomb lattice, terminated by oxygen atoms in Fe–W bridging positions. This 2D FeWO3 layer has a novel structure and stoichiometry and has no analogues to known bulk iron tungstate phases. It is theoretically predicted to exhibit a ferromagnetic electronic ground state with a Curie temperature of 95 K, as opposed to the antiferromagnetic behavior of bulk FeWO4 materials. PMID:27110319

  3. Compton profiles and electronic structure of monoclinic zinc and cadmium tungstates

    NASA Astrophysics Data System (ADS)

    Meena, B. S.; Heda, N. L.; Mund, H. S.; Ahuja, B. L.

    2015-12-01

    We report the first ever Compton scattering study of ZnWO4 and CdWO4 using 20 Ci 137Cs Compton spectrometer at momentum resolution of 0.34 a.u. To compare the experimental Compton profiles, we have also deduced the momentum densities using density functional theory (DFT) within linear combination of atomic orbitals (LCAO) methods. It is seen that the experimental Compton profiles of both the tungstates give a better agreement with LCAO-DFT calculations within generalized gradient approximation (GGA) employing Perdew-Becke-Ernzerhof (PBE) exchange and correlation energies than other approximations included in the present work. Further, energy bands, density of states (DOS) and band gaps have also been calculated using LCAO-DFT-GGA-PBE scheme and full potential linearized augmented plane wave method. Both the computational schemes show a semiconducting nature of both the tungstates, with a direct band gap at Y point of Brillouin zone. Further, a relative nature of bonding on equal-valence-electron-density scale shows more covalent character in ZnWO4 than CdWO4 which reconciles with the conclusions drawn using integrated DOS and Mulliken's population data.

  4. Simultaneous speciation analysis of chromate, molybdate, tungstate and vanadate in welding fume alkaline extracts by HPLC-ICP-MS.

    PubMed

    Ščančar, Janez; Berlinger, Balázs; Thomassen, Yngvar; Milačič, Radmila

    2015-09-01

    A novel analytical procedure was developed for the simultaneous speciation analysis of chromate, molybdate, tungstate and vanadate by anion-exchange high performance liquid chromatography hyphenated to inductively coupled plasma mass spectrometry (HPLC-ICP-MS). Linear gradient elution from 100% water to 100% 0.7 M NaCl was applied for chromatographic separation of metal species. In standard aqueous solution at neutral pH molybdate, tungstate and vanadate exist in several aqueous species, while chromate is present as a single CrO4(2-) species. Consequently, only chromate can be separated from this solution in a sharp chromatographic peak. For obtaining sharp chromatographic peaks for molybdate, tungstate and vanadate, the pH of aqueous standard solutions was raised to 12. At highly alkaline conditions single CrO4(2-), MoO4(2-) and WO4(2-) are present and were eluted in sharp chromatographic peaks, while VO4(3-) species, which predominates at pH 12 was eluted in slightly broaden peak. In a mixture of aqueous standard solutions (pH 12) chromate, molybdate, tungstate and vanadate were eluted at retention times from 380 to 420 s, 320 to 370 s, 300 to 350 s and 240 to 360 s, respectively. Eluted species were simultaneously detected on-line by ICP-MS recording m/z 52, 95, 182 and 51. The developed procedure was successfully applied to the analysis of leachable concentrations of chromate, molybdate, tungstate and vanadate in alkaline extracts (2% NaOH+3% Na2CO3) of manual metal arc (MMA) welding fumes loaded on filters. Good repeatability and reproducibility of measurement (RSD±3.0%) for the investigated species were obtained in both aqueous standard solutions (pH 12) and in alkaline extracts of welding fumes. Low limits of detection (LODs) were found for chromate (0.02 ng Cr mL(-1)), molybdate (0.1 ng Mo mL(-1)), tungstate (0.1 ng W mL(-1)) and vanadate (0.2 ng V mL(-1)). The accuracy of analytical procedure for the determination of chromate was checked by analysis of

  5. 21 CFR 184.1137 - Ammonium carbonate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... sublimation of a mixture of ammonium sulfate and calcium carbonate and occurs as a white powder or a hard... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ammonium carbonate. 184.1137 Section 184.1137 Food... GRAS § 184.1137 Ammonium carbonate. (a) Ammonium carbonate ((NH4)2CO3, CAS Reg. No. 8000-73-5) is...

  6. 21 CFR 556.375 - Maduramicin ammonium.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Tolerances for Residues of New Animal Drugs § 556.375 Maduramicin ammonium. A tolerance is established for residues of maduramicin ammonium in chickens as follows: (a) A tolerance for maduramicin ammonium...

  7. 21 CFR 556.375 - Maduramicin ammonium.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Tolerances for Residues of New Animal Drugs § 556.375 Maduramicin ammonium. A tolerance is established for residues of maduramicin ammonium in chickens as follows: (a) A tolerance for maduramicin ammonium...

  8. 21 CFR 556.375 - Maduramicin ammonium.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... residues of maduramicin ammonium in chickens as follows: (a) A tolerance for maduramicin ammonium (marker residue) in chickens is 0.38 parts per million in fat (target tissue). A tolerance refers to the... animals. (b) The safe concentrations for total maduramicin ammonium residues in uncooked edible...

  9. 21 CFR 556.375 - Maduramicin ammonium.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Tolerances for Residues of New Animal Drugs § 556.375 Maduramicin ammonium. A tolerance is established for residues of maduramicin ammonium in chickens as follows: (a) A tolerance for maduramicin ammonium...

  10. 21 CFR 582.1141 - Ammonium phosphate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Ammonium phosphate. 582.1141 Section 582.1141 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1141 Ammonium phosphate. (a) Product. Ammonium phosphate (mono- and dibasic). (b)...

  11. 21 CFR 582.1141 - Ammonium phosphate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Ammonium phosphate. 582.1141 Section 582.1141 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1141 Ammonium phosphate. (a) Product. Ammonium phosphate (mono- and dibasic). (b)...

  12. 21 CFR 184.1138 - Ammonium chloride.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    .... No. 12125-02-9) is produced by the reaction of sodium chloride and an ammonium salt in solution. The less soluble sodium salt separates out at elevated temperatures, and ammonium chloride is recovered... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ammonium chloride. 184.1138 Section 184.1138...

  13. 21 CFR 184.1138 - Ammonium chloride.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    .... No. 12125-02-9) is produced by the reaction of sodium chloride and an ammonium salt in solution. The less soluble sodium salt separates out at elevated temperatures, and ammonium chloride is recovered... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ammonium chloride. 184.1138 Section 184.1138...

  14. 21 CFR 184.1138 - Ammonium chloride.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    .... No. 12125-02-9) is produced by the reaction of sodium chloride and an ammonium salt in solution. The less soluble sodium salt separates out at elevated temperatures, and ammonium chloride is recovered... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ammonium chloride. 184.1138 Section 184.1138...

  15. 21 CFR 184.1138 - Ammonium chloride.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    .... No. 12125-02-9) is produced by the reaction of sodium chloride and an ammonium salt in solution. The less soluble sodium salt separates out at elevated temperatures, and ammonium chloride is recovered... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ammonium chloride. 184.1138 Section 184.1138...

  16. 21 CFR 582.1143 - Ammonium sulfate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Ammonium sulfate. 582.1143 Section 582.1143 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1143 Ammonium sulfate. (a) Product. Ammonium sulfate. (b) Conditions of use. This...

  17. 21 CFR 582.1143 - Ammonium sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Ammonium sulfate. 582.1143 Section 582.1143 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1143 Ammonium sulfate. (a) Product. Ammonium sulfate. (b) Conditions of use. This...

  18. 21 CFR 582.1143 - Ammonium sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Ammonium sulfate. 582.1143 Section 582.1143 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1143 Ammonium sulfate. (a) Product. Ammonium sulfate. (b) Conditions of use. This...

  19. 21 CFR 582.1143 - Ammonium sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Ammonium sulfate. 582.1143 Section 582.1143 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1143 Ammonium sulfate. (a) Product. Ammonium sulfate. (b) Conditions of use. This...

  20. 21 CFR 582.1143 - Ammonium sulfate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Ammonium sulfate. 582.1143 Section 582.1143 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1143 Ammonium sulfate. (a) Product. Ammonium sulfate. (b) Conditions of use. This...

  1. Extraction of urea and ammonium ion

    NASA Technical Reports Server (NTRS)

    Anselmi, R. T.; Husted, R. R.; Schulz, J. R.

    1977-01-01

    Water purification system keeps urea and ammonium ion concentration below toxic limits in recirculated water of closed loop aquatic habitat. Urea is first converted to ammonium ions and carbon dioxide by enzygmatic action. Ammonium ions are removed by ion exchange. Bioburden is controlled by filtration through 0.45 micron millipore filters.

  2. 21 CFR 582.1141 - Ammonium phosphate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Ammonium phosphate. 582.1141 Section 582.1141 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1141 Ammonium phosphate. (a) Product. Ammonium phosphate (mono- and dibasic). (b)...

  3. 21 CFR 582.1141 - Ammonium phosphate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Ammonium phosphate. 582.1141 Section 582.1141 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1141 Ammonium phosphate. (a) Product. Ammonium phosphate (mono- and dibasic). (b)...

  4. 21 CFR 582.1141 - Ammonium phosphate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Ammonium phosphate. 582.1141 Section 582.1141 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1141 Ammonium phosphate. (a) Product. Ammonium phosphate (mono- and dibasic). (b)...

  5. Phase diagram of ammonium nitrate

    NASA Astrophysics Data System (ADS)

    Dunuwille, M.; Yoo, C. S.

    2014-05-01

    Ammonium Nitrate (AN) has often subjected to uses in improvised explosive devices, due to its wide availability as a fertilizer and its capability of becoming explosive with slight additions of organic and inorganic compounds. Yet, the origin of enhanced energetic properties of impure AN (or AN mixtures) is neither chemically unique nor well understood -resulting in rather catastrophic disasters in the past1 and thereby a significant burden on safety in using ammonium nitrates even today. To remedy this situation, we have carried out an extensive study to investigate the phase stability of AN at high pressure and temperature, using diamond anvil cells and micro-Raman spectroscopy. The present results confirm the recently proposed phase IV-to-IV' transition above 17 GPa2 and provide new constraints for the melting and phase diagram of AN to 40 GPa and 400 °C.

  6. BK channel activation by tungstate requires the β1 subunit extracellular loop residues essential to modulate voltage sensor function and channel gating.

    PubMed

    Fernández-Mariño, Ana I; Valverde, Miguel A; Fernández-Fernández, José M

    2014-07-01

    Tungstate, a compound with antidiabetic, antiobesity, and antihypertensive properties, activates the large-conductance voltage- and Ca(2+)-dependent K(+) (BK) channel containing either β1 or β4 subunits. The BK activation by tungstate is Mg(2+)-dependent and promotes arterial vasodilation, but only in precontracted mouse arteries expressing β1. In this study, we further explored how the β1 subunit participates in tungstate activation of BK channels. Activation of heterologously expressed human BKαβ1 channels in inside-out patches is fully dependent on the Mg(2+) sensitivity of the BK α channel subunit even at high (10 μM) cytosolic Ca(2+) concentration. Alanine mutagenesis of β1 extracellular residues Y74 or S104, which destabilize the active voltage sensor, greatly decreased the tungstate-induced left-shift of the BKαβ1 G-V curves in either the absence or presence of physiologically relevant cytosolic Ca(2+) levels (10 μM). The weakened tungstate activation of the BKαβ1Y74A and BKαβ1S104A mutant channels was not related to decreased Mg(2+) sensitivity. These results, together with previously published reports, support the idea that the putative binding site for tungstate-mediated BK channel activation is located in the pore-forming α channel subunit, around the Mg(2+) binding site. The role of β1 in tungstate-induced channel activation seems to rely on its interaction with the BK α subunit to modulate channel activity. Loop residues that are essential for the regulation of voltage sensor activation and gating of the BK channel are also relevant for BK activation by tungstate. PMID:24158430

  7. Scintillation of lead tungstate crystal studied with single-electron beam from KUFEL

    SciTech Connect

    Rizwan, Mohamad Uozumi, Yusuke; Matsuo, Kazuki; Ohgaki, Hideaki; Kii, Toshiteru; Zen, Heishun; Tsamalaidze, Zviadi; Evtoukhovitch, Petr; Valentin, Samoilov

    2015-04-29

    Lead tungstate (PWO) crystal has a very fast response, high atomic density and high radiation hardness. Therefore, they are suitable to be used for high-energy nuclear data measurements under high-background circumstances. Although a good electron-ion separation with a pulse shape analysis technique is essential, scintillation pulse shapes have not been observed with electron beams of a wide energy range. A single-electron beam technique has been developed at Kyoto University Free Electron Laser (KUFEL), and electron beams of 4-38 MeV are available. During the experiments, single electron beams bombarded a PWO crystal. By using oscilloscope we observed scintillation pulses of a PWO crystal coupled with a photomultiplier tube. Measured spectra were compared with the simulation code of EGS5 to analyze scattering effects. As the result, the pulse amplitudes show good linearity and the pulse shapes are almost constant in the observed energy range.

  8. Lead Tungstate Crystals for the Cms Electromagnetic Calorimeter at the Lhc

    NASA Astrophysics Data System (ADS)

    Dafinei, Ioan

    2002-11-01

    With its over 80,000 scintillating lead tungstate PbWO4 (PWO) crystals the CMS electromagnetic calorimeter (ECAL) will be the largest one ever constructed. It was designed to work in the demanding LHC environment and give a resolution of 0.5% for photon energies above 50 GeV/c. An important R & D effort was necessary in order to guarantee the production of PWO crystals able to satisfy such challenging constraints. The performance of the pre-production crystal batches (about 6000 barrel crystals) is consistent with the very strict quality parameters defined by the ECAL Collaboration. The meaning of quality controls as well as the main characteristics of these crystals are discussed. More, recent developments in the PWO crystal growth technology may speedup the crystal supplying for the ECAL construction.

  9. Scintillation of lead tungstate crystal studied with single-electron beam from KUFEL

    NASA Astrophysics Data System (ADS)

    Rizwan, Mohamad; Uozumi, Yusuke; Matsuo, Kazuki; Ohgaki, Hideaki; Kii, Toshiteru; Zen, Heishun; Tsamalaidze, Zviadi; Evtoukhovitch, Petr; Valentin, Samoilov

    2015-04-01

    Lead tungstate (PWO) crystal has a very fast response, high atomic density and high radiation hardness. Therefore, they are suitable to be used for high-energy nuclear data measurements under high-background circumstances. Although a good electron-ion separation with a pulse shape analysis technique is essential, scintillation pulse shapes have not been observed with electron beams of a wide energy range. A single-electron beam technique has been developed at Kyoto University Free Electron Laser (KUFEL), and electron beams of 4-38 MeV are available. During the experiments, single electron beams bombarded a PWO crystal. By using oscilloscope we observed scintillation pulses of a PWO crystal coupled with a photomultiplier tube. Measured spectra were compared with the simulation code of EGS5 to analyze scattering effects. As the result, the pulse amplitudes show good linearity and the pulse shapes are almost constant in the observed energy range.

  10. Fast synthesis and morphology control of lead tungstate microcrystals via a microwave-assisted method

    SciTech Connect

    Wang Guizhen; Hao Chuncheng

    2009-02-04

    Lead tungstate (PbWO{sub 4}) microcrystals with different morphologies, such as tetragonal flowerlike, amygdaloidal, and multiple-lamellar, have been successfully synthesized via a simple microwave-assisted method. Various factors, such as the pH value and the concentration of the cetyltrimethylammonium bromide (CTAB), play an important role in the morphological control of PbWO{sub 4} microcrystals. The products were characterized by the techniques of powder X-ray diffraction, field emission scanning electron microscopy, and transmission electron microscopy. The possible formation mechanisms of PbWO{sub 4} samples of various morphologies were discussed. The luminescence properties of the final products were investigated and the as-prepared PbWO{sub 4} microcrystals showed special room-temperature photoluminescence intensity compared to the solid structures.

  11. Lasing properties of new Nd 3+-doped tungstate, molybdate, and fluoride materials under selective optical pumping

    NASA Astrophysics Data System (ADS)

    Šulc, Jan; Jelínkova, Helena; Basiev, Tolstoban T.; Doroschenko, Maxim E.; Ivleva, Ludmila I.; Osiko, Vyacheslav V.; Zverev, Peter G.

    2006-02-01

    The purpose of this work was to determine the relative efficiencies of new Nd 3+-doped laser active/Raman - tungstate, molybdate, and fluoride - materials (SrWO 4, PbWO 4, BaWO 4, SrMoO 4, PbMoO 4, SrF II, and LaF 3) under selective longitudinal optical pumping by the alexandrite (~750nm), or diode (~800nm) laser. Crystals with various length, orientations and active ions concentrations were tested. To optimize the output of the tested lasers a set of input dichroic and output dielectric mirrors with different reflectivities were used. For realized lasers operating at pulsed free-running regime, threshold energy, slope efficiency, emission wavelength, and radiation polarization were determined. For each crystal, fluorescence lifetime and absorption coefficient under given pumping were established. The slope efficiency in case of Nd 3+:PbMoO 4 laser at wavelength 1054nm was measured to be 54.3% with total efficiency of 46% which is the best result obtained for all new tested crystals. For Nd 3+ doped SrWO 4, PbWO 4, and BaWO 4 crystals simultaneous laser and self-Raman emission were demonstrated in Q-switched regime. Thus newly proposed laser Raman crystals demonstrate high efficiency for Nd 3+ laser oscillations comparable with well known and widely used Nd:KGW crystal. Further improvement in the quality of tungstate and molybdate type crystals should result in further increase in lasing efficiency at 1.06μm wavelength. Self Raman frequency conversion of Nd 3+-laser oscillations in these crystals should result in high efficient pulse shortening, high peak power and new wavelengths in 1.2-1.5μm wavelength region.

  12. Diode-pumped ytterbium-doped phosphate and tungstate regenerative amplifiers and ancillary investigations

    NASA Astrophysics Data System (ADS)

    Liu, Hsiao-Hua

    This thesis focuses on the development of directly diode- pumped solid-state regenerative laser amplifiers. Our purpose is to build a compact, simple, reliable, and economical subpicosecond laser system by employing a direct diode-pumping scheme for real-world applications such as medical surgeries and micromachining. Ytterbium- doped phosphate glass (QX/Yb) and ytterbium-doped tungstate crystals (Yb:KYW and Yb:KGW) are used as the amplifier gain media, and their laser properties are discussed and compared with other ytterbium-doped materials. The same oscillator, stretcher, and compressor are used with each amplifier presented. Both end- and side-pumping configurations are implemented and compared wherever possible. Typically, an end-pumped laser has a higher efficiency, whereas a side-pumped laser has a simpler, and thus more compact setup. To improve the efficiency of a side-pumped laser, we have proposed and demonstrated a novel pumping scheme with the QX/Yb, amplifier. To match the elliptical beam from the pump diodes, we have designed and built cavities with an elliptical fundamental mode by using cylindrical optics. Millijoule, subpicosecond pulses have been produced from our QX/Yb regenerative amplifier using the proposed pumping scheme and an elliptic-mode cavity. The diode- pumped ytterbium-doped tungstate regenerative amplifiers in this thesis produced subpicosecond pulses with at least tens of microjoules of pulse energy at a kHz repetition rate, also using a cavity with an elliptical fundamental mode. A self-starting Kerr-lens mode-locked Yb:KYW oscillator directly pumped by diodes and a low- repetition-rate Yb:KGW regenerative amplifier pumped by a flashlamp-pumped Ti:sapphire laser are also presented as ancillary studies.

  13. On the nature of defect states in tungstate nanoflake arrays as promising photoanodes in solar fuel cells.

    PubMed

    Mohamed, Aya M; Amer, Ahmad W; AlQaradawi, Siham Y; Allam, Nageh K

    2016-08-10

    An electrochemical method is presented to study the nature of the defect states in sub-stoichiometric tungsten oxide nanoflake photoanodes used in water splitting. First, stoichiometric/sub-stoichiometric tungstate nanoflake arrays were deliberately developed via annealing under different atmospheres (air, O2, and H2) in different sequences. UV-Vis diffuse reflectance spectra and Tauc analysis indicated the presence of oxygen vacancies, which was also confirmed via XRD and Raman analysis, with samples annealed in an air/O2 sequence resulting in the most stoichiometric monoclinic structures. A defect sensitivity factor was proposed to explain the nature of defects whether they are deep or shallow. Mott-Schottky analysis was used to confirm the expected defect donor densities, as well as to confirm the nature of the developed oxygen vacancy defect states. The tungstate photoanodes were tested in photoelectrochemical water splitting cells and their photoconversion efficiency was demonstrated and discussed in detail. PMID:27453354

  14. Toward a mid-infrared femtosecond laser system with suspended-core tungstate-tellurite glass fibers.

    PubMed

    Anashkina, E A; Andrianov, A V; Dorofeev, V V; Kim, A V

    2016-06-10

    A simple design of a fiber laser system for generating high-quality pulses with a duration of order 100 fs with ultrabroad wavelength tunability in the 2-5 μm range is discussed. This design incorporates conventional fs near-IR lasers and specially developed tungstate-tellurite fibers with two zero-dispersion wavelengths (ZDW) and relies on nonlinear wavelength conversion via either soliton self-frequency shift (SSFS) or red-shifted dispersive wave (DW) generation. The fiber parameters needed for such optical conversion have been scanned numerically and showed a possibility of SSFS beyond 4 μm and of DW generation beyond 5 μm. We have also studied and prepared tungstate-tellurite glasses and preforms that are highly stable against crystallization, exhibit extremely low level of hydroxyl groups absorption, and from which the suspended-core two-ZDW fibers can be manufactured. PMID:27409007

  15. Assessing the performance under ionising radiation of lead tungstate scintillators for EM calorimetry in the CLAS12 Forward Tagger

    NASA Astrophysics Data System (ADS)

    Fegan, S.; Auffray, E.; Battaglieri, M.; Buchanan, E.; Caiffi, B.; Celentano, A.; Colaneri, L.; D`Angelo, A.; De Vita, R.; Dormenev, V.; Fanchini, E.; Lanza, L.; Novotny, R. W.; Parodi, F.; Rizzo, A.; Sokhan, D.; Tarasov, I.; Zonta, I.

    2015-07-01

    The well-established technology of electromagnetic calorimetry using Lead Tungstate crystals has recently seen an upheaval, with the closure of one of the most experienced large-scale suppliers of such crystals, the Bogoroditsk Technical Chemical Plant (BTCP), which was instrumental in the development of mass production procedures for PWO-II, the current benchmark for this scintillator. Obtaining alternative supplies of Lead Tungstate crystals matching the demanding specifications of contemporary calorimeter devices now presents a significant challenge to detector research and development programmes. In this paper we describe a programme of assessment carried out for the selection, based upon the performance under irradiation, of Lead Tungstate crystals for use in the Forward Tagger device, part of the CLAS12 detector in Hall B at Jefferson Lab. The crystals tested were acquired from SICCAS, the Shanghai Institute of Ceramics, Chinese Academy of Sciences. The tests performed are intended to maximise the performance of the detector within the practicalities of the crystal manufacturing process. Results of light transmission, before and after gamma ray irradiation, are presented and used to calculate dk, the induced radiation absorption coefficient, at 420 nm, the peak of the Lead Tungstate emission spectrum. Results for the SICCAS crystals are compared with identical measurements carried out on Bogoroditsk samples, which were acquired for the Forward Tagger development program before the closure of the facility. Also presented are a series of tests performed to determine the feasibility of recovering radiation damage to the crystals using illumination from an LED, with such illumination available in the Forward Tagger from a light monitoring system integral to the detector.

  16. Steady-state Raman gain coefficients of potassium-gadolinium tungstate at the wavelength of 532 nm

    NASA Astrophysics Data System (ADS)

    Chulkov, R.; Markevich, V.; Orlovich, V.; El-Desouki, M.

    2015-12-01

    Stokes generation has been considered under the Fourier-limited nanosecond pulse excitation to find Raman gain coefficients in potassium-gadolinium tungstate. Data of numerical simulation under spontaneous Stokes initiation, light diffraction, and optical feedback have been compared with experimental results to reveal coefficient values of 14 ± 3 and 11 ± 3 cm/GW for the p[mm]p and p[gg]p sample orientations, respectively, at 532 nm wavelength.

  17. Ammonium assmilation in spruce ectomycorrhizas

    SciTech Connect

    Chalot, M.; Brun, A.; Botton, B. ); Stewart, G. )

    1990-05-01

    Assimilation of labelled NH{sub 4}{sup +} into amino acids has been followed in ectomycorrhizal roots of spruce. Over an 18 h period of NH{sub 4}{sup +} feeding, Gln, Glu and Ala became the most abundant amino acids. Gln was also the most highly labelled amino acid during the experiment, followed by Glu and Ala. This result indicates that Gln synthesis is an important ammonium utilization reaction in spruce mycorrhizas. Addition of MSX to NH{sub 4}{sup +} fed mycorrhizas caused an inhibition of Gln accumulation with a corresponding increase in Glu, Ala and Asn levels. The supply of MSX induced a sharp diminution of {sup 15}N enrichment in both amino and amido groups of glutamine. In contrast, the {sup 15}N incorporation into Glu and derivatives (Ala and Asp) remained very high. This study demonstrates that the fungal glutamate dehydrogenase is quite operative in spruce ectomycorrhizas since it is able to sustain ammonium assimilation when glutamine synthetase is inhibited.

  18. Structural study of ammonium metatungstate

    SciTech Connect

    Christian, Joel B. Whittingham, M. Stanley

    2008-08-15

    Several techniques have been used to study the structure of the Keggin-type polyoxometalate salt ammonium metatungstate (AMT)-(NH{sub 4}){sub 6}[H{sub 2}W{sub 12}O{sub 40}]*nH{sub 2}O, a potential fuel cell catalyst. The dehydrated salt is comprised of a mixture of crystallites of different unit cells in a centered eutactic cubic configuration, with an average unit cell of a{approx_equal}12.295. Varied orientations of the Keggin ions in the cubic arrangement create the differences, and orientational variation within each unit cell size represents an energy well. Progressive hydration of each crystallite leads to expansion of the lattice, with the degree of expansion depending on the locations of the water added in relation to the Keggin ion, which is influenced by cation location and hydrogen bonding. The structural hypothesis is supported by electron diffraction of single and multicrystal samples, by powder density measurements, X-ray powder diffraction studies, synchrotron powder X-ray diffraction, and a priori structural modeling studies. Based on the structure, projected active site densities are compared with nanostructured platinum catalysts for fuel cell application. - Graphical abstract: The structure of ammonium metatungstate powders are highly dependent on hydration and POM molecule rotation, with cation and hydrogen bonding forces directing a mixture of structures that have been studied with bulk and single-crystal methods. The illustration shows Monte Carlo simulated anion structural disorder for the fully dehydrated form of the title compound.

  19. Phase Diagram of Ammonium Nitrate

    NASA Astrophysics Data System (ADS)

    Dunuwille, Mihindra; Yoo, Choong-Shik

    2013-06-01

    Ammonium Nitrate (AN) has often been subjected to uses in improvised explosive devices, due to its wide availability as a fertilizer and its capability of becoming explosive with slight additions of organic and inorganic compounds. Yet, the origin of enhanced energetic properties of impure AN (or AN mixtures) is neither chemically unique nor well understood - resulting in rather catastrophic disasters in the past1 and thereby a significant burden on safety, in using ammonium nitrates even today. To remedy this situation, we have carried out an extensive study to investigate the phase stability of AN, in different chemical environments, at high pressure and temperature, using diamond anvil cells and micro-Raman spectroscopy. The present results confirm the recently proposed phase IV-to-IV' transition above 15 GPa2 and provide new constraints for the melting and phase diagram of AN to 40 GPa and 673 K. The present study has been supported by the U.S. DHS under Award Number 2008-ST-061-ED0001.

  20. 49 CFR 176.410 - Division 1.5 materials, ammonium nitrate and ammonium nitrate mixtures.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 49 Transportation 2 2013-10-01 2013-10-01 false Division 1.5 materials, ammonium nitrate and ammonium nitrate mixtures. 176.410 Section 176.410 Transportation Other Regulations Relating to... nitrate and ammonium nitrate mixtures. (a) This section prescribes requirements to be observed...

  1. 49 CFR 176.410 - Division 1.5 materials, ammonium nitrate and ammonium nitrate mixtures.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 49 Transportation 2 2014-10-01 2014-10-01 false Division 1.5 materials, ammonium nitrate and ammonium nitrate mixtures. 176.410 Section 176.410 Transportation Other Regulations Relating to... nitrate and ammonium nitrate mixtures. (a) This section prescribes requirements to be observed...

  2. 49 CFR 176.410 - Division 1.5 materials, ammonium nitrate and ammonium nitrate mixtures.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 49 Transportation 2 2012-10-01 2012-10-01 false Division 1.5 materials, ammonium nitrate and ammonium nitrate mixtures. 176.410 Section 176.410 Transportation Other Regulations Relating to... nitrate and ammonium nitrate mixtures. (a) This section prescribes requirements to be observed...

  3. 49 CFR 176.410 - Division 1.5 materials, ammonium nitrate and ammonium nitrate mixtures.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 49 Transportation 2 2010-10-01 2010-10-01 false Division 1.5 materials, ammonium nitrate and ammonium nitrate mixtures. 176.410 Section 176.410 Transportation Other Regulations Relating to... nitrate and ammonium nitrate mixtures. (a) This section prescribes requirements to be observed...

  4. 49 CFR 176.410 - Division 1.5 materials, ammonium nitrate and ammonium nitrate mixtures.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 49 Transportation 2 2011-10-01 2011-10-01 false Division 1.5 materials, ammonium nitrate and ammonium nitrate mixtures. 176.410 Section 176.410 Transportation Other Regulations Relating to... nitrate and ammonium nitrate mixtures. (a) This section prescribes requirements to be observed...

  5. Equilibrium studies of sodium-ammonium potassium-ammonium, and calcium-ammonium exchanges on clinoptilolite zeolite

    SciTech Connect

    Jama, M.A.; Yuecel, H. )

    1989-12-01

    Forward and reverse ion-exchange isotherms for the binary sodium-ammonium, potassium-ammonium, and calcium-ammonium systems on clinoptilolite have been measured in aqueous solutions at a total concentration of 0.1 equiv/dm{sup 3} and at 298 K. Prior to exchange experiments it was attempted to prepare homoionic forms of the zeolite by exhaustive treatments with appropriate salt solutions of cations. With no binary exchanges, full replacement of the cation by the ammonium ion is observed, which conflicts with some earlier work on clinoptilolite. Despite the observed partial exchange levels, clinoptilolite shows a very high preference for ammonium ion over sodium and calcium but not over potassium. Thermodynamic values for the exchanges were calculated and compared with data in the literature. Both the selectivity and thermodynamic affinity sequence, in agreement with previous work reported in the literature, are K{sup +} > NH{sub 4}{sup +} > Na{sup +} > Ca{sup 2+}.

  6. 76 FR 46907 - Ammonium Nitrate Security Program

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-03

    ...This proposed rule would implement anti-terrorism measures to better secure the homeland. The Department of Homeland Security would regulate the sale and transfer of ammonium nitrate pursuant to section 563 of the Fiscal Year 2008 Department of Homeland Security Appropriations Act with the purpose of preventing the use of ammonium nitrate in an act of terrorism. This proposed rule seeks......

  7. Biodegradation of rocket propellant waste, ammonium perchlorate

    NASA Technical Reports Server (NTRS)

    Naqvi, S. M. Z.; Latif, A.

    1975-01-01

    The short term effects of ammonium perchlorate on selected organisms were studied. A long term experiment was also designed to assess the changes incurred by ammonium perchlorate on the nitrogen and chloride contents of soil within a period of 3 years. In addition, an attempt was made to produce methane gas from anaerobic fermentation of the aquatic weed, Alternanthera philoxeroides.

  8. 76 FR 62311 - Ammonium Nitrate Security Program

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-10-07

    ... FR 64280 (advance notice of proposed rulemaking); 76 FR 46908 (notice of proposed rulemaking... Program Web site in mid-October at http://www.dhs.gov/ files/ ] programs/ammonium-nitrate-security-program...; ] DEPARTMENT OF HOMELAND SECURITY Office of the Secretary 6 CFR Part 31 RIN 1601-AA52 Ammonium Nitrate...

  9. Ammonium nonanoate broadcast application over onions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Ammonium nonanoate occurs in nature and is primarily formed from biodegradation of higher fatty acids. Racer (40% ammonium nonaoate) is a potential contact herbicide for weed control in organic crop production. Field research was conducted in southeast Oklahoma (Atoka County, Lane, OK) to determin...

  10. Evolution of Electrogenic Ammonium Transporters (AMTs)

    PubMed Central

    McDonald, Tami R.; Ward, John M.

    2016-01-01

    The ammonium transporter gene family consists of three main clades, AMT, MEP, and Rh. The evolutionary history of the AMT/MEP/Rh gene family is characterized by multiple horizontal gene transfer events, gene family expansion and contraction, and gene loss; thus the gene tree for this family of transporters is unlike the organismal tree. The genomes of angiosperms contain genes for both electrogenic and electroneutral ammonium transporters, but it is not clear how far back in the land plant lineage electrogenic ammonium transporters occur. Here, we place Marchantia polymorpha ammonium transporters in the AMT/MEP/Rh phylogeny and we show that AMTs from the liverwort M. polymorpha are electrogenic. This information suggests that electrogenic ammonium transport evolved at least as early as the divergence of bryophytes in the land plant lineage. PMID:27066024

  11. Evolution of Electrogenic Ammonium Transporters (AMTs).

    PubMed

    McDonald, Tami R; Ward, John M

    2016-01-01

    The ammonium transporter gene family consists of three main clades, AMT, MEP, and Rh. The evolutionary history of the AMT/MEP/Rh gene family is characterized by multiple horizontal gene transfer events, gene family expansion and contraction, and gene loss; thus the gene tree for this family of transporters is unlike the organismal tree. The genomes of angiosperms contain genes for both electrogenic and electroneutral ammonium transporters, but it is not clear how far back in the land plant lineage electrogenic ammonium transporters occur. Here, we place Marchantia polymorpha ammonium transporters in the AMT/MEP/Rh phylogeny and we show that AMTs from the liverwort M. polymorpha are electrogenic. This information suggests that electrogenic ammonium transport evolved at least as early as the divergence of bryophytes in the land plant lineage. PMID:27066024

  12. Investigation of oxygen vacancy and photoluminescence in calcium tungstate nanophosphors with different particle sizes

    SciTech Connect

    Li, Yezhou; Wang, Zhaofeng; Sun, Luyi; Wang, Zhilong; Wang, Shiqin; Liu, Xiong; Wang, Yuhua

    2014-02-01

    Highlights: • CaWO{sub 4} nanophosphors with different particle sizes were prepared by hydrothermal processes through controlling the concentration of surfactant. • Green emission band of oxygen vacancy in CaWO{sub 4} nanophosphor was clearly observed upon the irradiation of 350 nm excitation. • The concentration of oxygen vacancy in CaWO{sub 4} nanophosphor could be increased by reducing its size. - Abstract: Calcium tungstate (CaWO{sub 4}) nanophosphors with the particle sizes from 35 to 90 nm were synthesized by a hydrothermal process through exactly controlling the pre-treated conditions. The influence of particle size on oxygen vacancy and photoluminescence properties in CaWO{sub 4} nanophosphors was investigated and discussed. The crystal structure of the CaWO{sub 4} nanophosphors presented a certain level of distortion due to the high concentration of oxygen vacancy. Under 350 nm excitation, a clear green emission aroused by oxygen vacancy was observed. The possible luminescence processes for the matrix and oxygen vacancy were proposed. The luminescence spectra of the nanophosphors revealed that the emission and absorption intensity aroused by oxygen vacancy were both enhanced when the size is decreased. On the basis of the above results, the essential relationship between particle size and oxygen vacancy in CaWO{sub 4} nanophosphors was concluded that the concentration of oxygen vacancy could be increased by reducing its size, which was further confirmed by decay lifetimes.

  13. Zirconium tungstate/epoxy nanocomposites: effect of nanoparticle morphology and negative thermal expansivity.

    PubMed

    Wu, Hongchao; Rogalski, Mark; Kessler, Michael R

    2013-10-01

    The ability to tailor the coefficient of thermal expansion (CTE) of a polymer is essential for mitigating thermal residual stress and reducing microcracks caused by CTE mismatch of different components in electronic applications. This work studies the effect of morphology and thermal expansivity of zirconium tungstate nanoparticles on the rheological, thermo-mechanical, dynamic-mechanical, and dielectric properties of ZrW2O8/epoxy nanocomposites. Three types of ZrW2O8 nanoparticles were synthesized under different hydrothermal conditions and their distinct properties were characterized, including morphology, particle size, aspect ratio, surface area, and CTE. Nanoparticles with a smaller particle size and larger surface area led to a more significant reduction in gel-time and glass transition temperature of the epoxy nanocomposites, while a higher initial viscosity and significant shear thinning behavior was found in prepolymer suspensions containing ZrW2O8 with larger particle sizes and aspect ratios. The thermo- and dynamic-mechanical properties of epoxy-based nanocomposites improved with increasing loadings of the three types of ZrW2O8 nanoparticles. In addition, the introduced ZrW2O8 nanoparticles did not negatively affect the dielectric constant or the breakdown strength of the epoxy resin, suggesting potential applications of ZrW2O8/epoxy nanocomposites in the microelectronic insulation industry. PMID:24070222

  14. Effect of tri- and tetravalent metal doping on the electrochemical properties of lanthanum tungstate proton conductors.

    PubMed

    Porras-Vázquez, J M; dos Santos-Gómez, L; Marrero-López, D; Slater, P R; Masó, N; Magrasó, A; Losilla, Enrique R

    2016-02-21

    Rare-earth tungstates (La(28-y)W(4+y)O(54+δ)□(2-δ)) have attracted attention recently because of their relatively high proton-electron conductivity and high stability in a CO2 environment. Since doping on the tungsten-site may increase the conductivity, a new series of compounds with composition La(5.5)W(1-x)M(x)O(11.25-δ) (M = Al, Ti and Zr; x = 0, 0.05 and 0.10) have been investigated. The crystal structure of these materials has been studied using X-ray and time-of-flight neutron powder diffraction by Rietveld analysis. The concentration of oxygen vacancies for hydration in the structure has been indirectly determined by thermogravimetric analysis, and the total conductivity in several pO2, pH2O and pD2O atmospheres has been studied by impedance spectroscopy. An increase in the conductivity is observed, ranging from 4.1 mS cm(-1) for the undoped sample to 9.2 mS cm(-1) for La(5.5)W(0.9)Ti(0.1)O(11.25-δ), in wet N2 at 800 °C. PMID:26776842

  15. ROLE OF TUNGSTEN IN THE AQUEOUS PHASE HYDRODEOXYGENATION OF ETHYLENE GLYCOL ON TUNGSTATED ZIRCONIA SUPPORTED PALLADIUM

    SciTech Connect

    Marin-Flores, Oscar G.; Karim, Ayman M.; Wang, Yong

    2014-11-15

    The focus of the present work was specifically on the elucidation of the role played by tungsten on the catalytic activity and selectivity of tungstated zirconia supported palladium (Pd-mWZ) for the aqueous phase hydrodeoxygenation (APHDO) of ethylene glycol (EG). Zirconia supported palladium (Pd-mZ) was used as reference. The catalysts were prepared via incipient wet impregnation and characterized using X-ray diffraction (XRD), temperature-programmed reduction (TPR), CO pulse chemisorption, CO-DRIFTS, ammonia temperature-programmed desorption (NH3-TPD) and pyridine adsorption. The presence of W results in larger Pd particles on supported Pd catalysts, i.e., 0.9 and 6.1 nm Pd particles are for Pd-mZ and Pd-mWZ, respectively. For comparison purposes, the activity of the catalytic materials used in this work was obtained using a well-defined set of operating conditions. The catalytic activity measurements show that the overall intrinsic activity of Pd particles on mWZ is 1.9 times higher than on mZ. APHDO process appears to be highly favored on Pd-mWZ whereas Pd-mZ exhibits a higher selectivity for reforming. This difference in terms of selectivity seems to be related to the high concentration of Brønsted acid sites and electron-deficient Pd species present on Pd-mWZ.

  16. Biodiesel synthesis catalyzed by transition metal oxides: ferric-manganese doped tungstated/molybdena nanoparticle catalyst.

    PubMed

    Alhassan, Fatah Hamid; Rashid, Umer; Taufiq-Yap, Yun Hin

    2015-01-01

    The solid acid Ferric-manganese doped tungstated/molybdena nananoparticle catalyst was prepared via impregnation reaction followed by calcination at 600°C for 3 h. The characterization was done using X-ray diffraction (XRD), Raman spectroscopy, thermal gravimetric analysis (TGA), temperature programmed desorption of NH3 (TPD-NH3), X-ray fluorescence (XRF), Transmission electron microscope (TEM) and Brunner-Emmett-Teller surface area measurement (BET). Moreover, dependence of biodiesel yield on the reaction variables such as the reaction temperature, catalyst loading, as well as molar ratio of methanol/oil and reusability were also appraised. The catalyst was reused six times without any loss in activity with maximum yield of 92.3% ±1.12 achieved in the optimized conditions of reaction temperature of 200°C; stirring speed of 600 rpm, 1:25 molar ratio of oil to alcohol, 6 % w/w catalyst loading as well as 8 h as time of the reaction. The fuel properties of WCOME's were evaluated, including the density, kinematic viscosity, pour point, cloud point and flash point whereas all properties were compared with the limits in the ASTM D6751 standard. PMID:25492234

  17. Studying radiation hardness of a cadmium tungstate crystal based radiation detector

    NASA Astrophysics Data System (ADS)

    Shtein, M. M.; Smekalin, L. F.; Stepanov, S. A.; Zatonov, I. A.; Tkacheva, T. V.; Usachev, E. Yu

    2016-06-01

    The given article considers radiation hardness of an X-ray detector used in production of non-destructive testing instruments and inspection systems. In the course of research, experiments were carried out to estimate radiation hardness of a detector based on cadmium tungstate crystal and its structural components individually. The article describes a layout of an experimental facility that was used for measurements of radiation hardness. The radiation dose dependence of the photodiode current is presented, when it is excited by a light flux of a scintillator or by an external light source. Experiments were carried out to estimate radiation hardness of two types of optical glue used in detector production; they are based on silicon rubber and epoxy. With the help of a spectrophotometer and cobalt gun, each of the glue samples was measured for a relative light transmission factor with different wavelengths, depending on the radiation dose. The obtained data are presented in a comprehensive analysis of the results. It was determined, which of the glue samples is most suitable for production of detectors working under exposure to strong radiation.

  18. Numerical simulation of photonic-crystal tellurite-tungstate glass fibres used in parametric fibre devices

    SciTech Connect

    Sokolov, V O; Plotnichenko, V G; Nazaryants, V O; Dianov, Evgenii M

    2006-01-31

    Using the MIT Photonic-Bands Package to calculate fully vectorial definite-mode eigenmodes of Maxwell's equations with periodic boundary conditions in a plane-wave basis, light propagation is simulated in fibres formed by point defects in two-dimensional periodic lattices of cylindrical holes in a glass or of glass tubes. The holes and gaps between tubes are assumed filled with air. Single-site hexagonal and square lattices are considered, which were most often studied both theoretically and experimentally and are used to fabricate silica photonic-crystal fibres. As a defect, a single vacancy is studied - the absent lattice site (one hole in a glass or one of the tubes are filled with the same glass) and a similar vacancy with nearest neighbours representing holes of a larger diameter. The obtained solutions are analysed by the method of effective mode area. The dependences of the effective refractive index and dispersion of the fundamental mode on the geometrical parameters of a fibre are found. The calculations are performed for tellurite-tungstate 80TeO{sub 2}-20WO{sub 3} glass fibres taking into account the frequency dispersion of the refractive index. (optical fibres)

  19. Compton profiles and Mulliken's populations of cobalt, nickel and copper tungstates: Experiment and theory

    NASA Astrophysics Data System (ADS)

    Meena, B. S.; Heda, N. L.; Kumar, Kishor; Bhatt, Samir; Mund, H. S.; Ahuja, B. L.

    2016-03-01

    We present the first ever studies on Compton profiles of AWO4 (A=Co, Ni and Cu) using 661.65 keV γ-rays emitted by 137Cs source. The experimental momentum densities have been employed to validate exchange and correlation potentials within linear combination of atomic orbitals (LCAO) method. Density functional theory (DFT) with local density approximation and generalized gradient approximation and also the hybridization of Hartree-Fock and DFT (B3LYP and PBE0) have been considered under LCAO scheme. The LCAO-B3LYP scheme is found to be in better agreement with the experimental data than other approximations considered in this work, suggesting applicability of B3LYP approach in predicting the electronic properties of these tungstates. The Mulliken's population (MP) data show charge transfer from Co/Ni/Cu and W to O atoms. The experimental profiles when normalized to same area show almost similar localization of 3d electrons (in real space) of Ni and Cu which is lower than that of Co in their AWO4 environment.

  20. Two-photon interband absorption coefficients in tungstate and molybdate crystals

    NASA Astrophysics Data System (ADS)

    Lukanin, V. I.; Karasik, A. Ya.

    2015-02-01

    Two-photon absorption (TPA) coefficients were measured in tungstate and molybdate crystals - BaWO4, KGW, CaMoO4, BaMoO4, CaWO4, PbWO4 and ZnWO4 upon different orientations of excitation polarization with respect to the crystallographic axes. Trains of 25 ps pulses with variable radiation intensities of third (349 nm) harmonics of passively mode-locked 1047 nm Nd:YLF laser were used for interband two-photon excitation of the crystals. It was suggested that in the case, when 349 nm radiation pumping energy exceeds the bandgap width (hν>Eg), the nonlinear excitation process can be considered as two-step absorption. The interband two-photon absorption in all the studied crystals induces the following one-photon absorption from the exited states, which affects the nonlinear process dynamics and leads to a hysteresis in the dependence of the transmission on the excitation intensity. This fact was taken into account under analysis of the experimental dependences of the reciprocal transmission on the excitation intensity. Laser excitation in the transparency region of the crystals caused stimulated Raman scattering (SRS) not for all the crystals studied. The measured nonlinear coefficients allowed us to explain the suppression of SRS in crystals as a result of competition between the SRS and TPA.

  1. 49 CFR 176.415 - Permit requirements for Division 1.5, ammonium nitrates, and certain ammonium nitrate fertilizers.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... nitrates, and certain ammonium nitrate fertilizers. 176.415 Section 176.415 Transportation Other... requirements for Division 1.5, ammonium nitrates, and certain ammonium nitrate fertilizers. (a) Except as... Captain of the Port (COTP). (1) Ammonium nitrate UN1942, ammonium nitrate fertilizers containing more...

  2. 49 CFR 176.415 - Permit requirements for Division 1.5, ammonium nitrates, and certain ammonium nitrate fertilizers.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... nitrates, and certain ammonium nitrate fertilizers. 176.415 Section 176.415 Transportation Other... requirements for Division 1.5, ammonium nitrates, and certain ammonium nitrate fertilizers. (a) Except as... Captain of the Port (COTP). (1) Ammonium nitrate UN1942, ammonium nitrate fertilizers containing more...

  3. 49 CFR 176.415 - Permit requirements for Division 1.5, ammonium nitrates, and certain ammonium nitrate fertilizers.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... nitrates, and certain ammonium nitrate fertilizers. 176.415 Section 176.415 Transportation Other... requirements for Division 1.5, ammonium nitrates, and certain ammonium nitrate fertilizers. (a) Except as... Captain of the Port (COTP). (1) Ammonium nitrate UN1942, ammonium nitrate fertilizers containing more...

  4. 49 CFR 176.415 - Permit requirements for Division 1.5, ammonium nitrates, and certain ammonium nitrate fertilizers.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... nitrates, and certain ammonium nitrate fertilizers. 176.415 Section 176.415 Transportation Other... requirements for Division 1.5, ammonium nitrates, and certain ammonium nitrate fertilizers. (a) Except as... Captain of the Port (COTP). (1) Ammonium nitrate UN1942, ammonium nitrate fertilizers containing more...

  5. 49 CFR 176.415 - Permit requirements for Division 1.5, ammonium nitrates, and certain ammonium nitrate fertilizers.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... nitrates, and certain ammonium nitrate fertilizers. 176.415 Section 176.415 Transportation Other... requirements for Division 1.5, ammonium nitrates, and certain ammonium nitrate fertilizers. (a) Except as... Captain of the Port (COTP). (1) Ammonium nitrate UN1942, ammonium nitrate fertilizers containing more...

  6. The nucleation kinetics of ammonium metavanadate precipitated by ammonium chloride

    NASA Astrophysics Data System (ADS)

    Du, Guangchao; Sun, Zhaohui; Xian, Yong; Jing, Han; Chen, Haijun; Yin, Danfeng

    2016-05-01

    The nucleation kinetics of ammonium metavanadate (NH4VO3) was investigated under conditions of the simulated process for precipitation of NH4VO3 from the vanadium-containing solution. Induction periods for the nucleation of NH4VO3 were experimentally determined as a function of supersaturation at temperatures from 30 to 45 °C. Using the classical nucleation theory, the interfacial tension between NH4VO3 and supersaturated solution, the nucleation rate and critical radius of nucleus for the homogeneous nucleation of NH4VO3 were estimated. With temperature increasing, the calculated interfacial tension gradually decreased from 29.78 mJ/m2 at 30 °C to 23.66 mJ/m2 at 45 °C. The nucleation rate was found to proportionally increase but the critical radius of nucleus exponentially decreased, with increase in supersaturation ratio at a constant temperature. The activation energy for NH4VO3 nucleation was obtained from the relationship between temperature and induction period, ranging from 79.17 kJ/mol at S=25 to 115.50 kJ/mol at S=15. FT-IR and Raman spectrum indicated that the crystals obtained in the precipitation process were NH4VO3.

  7. 21 CFR 73.1298 - Ferric ammonium ferrocyanide.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...) Identity. (1) The color additive ferric ammonium ferrocyanide is the blue pigment obtained by oxidizing... product is filtered, washed, and dried. The pigment consists principally of ferric ammonium...

  8. 21 CFR 73.1298 - Ferric ammonium ferrocyanide.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...) Identity. (1) The color additive ferric ammonium ferrocyanide is the blue pigment obtained by oxidizing... product is filtered, washed, and dried. The pigment consists principally of ferric ammonium...

  9. 21 CFR 73.1298 - Ferric ammonium ferrocyanide.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...) Identity. (1) The color additive ferric ammonium ferrocyanide is the blue pigment obtained by oxidizing... product is filtered, washed, and dried. The pigment consists principally of ferric ammonium...

  10. 21 CFR 73.1298 - Ferric ammonium ferrocyanide.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...) Identity. (1) The color additive ferric ammonium ferrocyanide is the blue pigment obtained by oxidizing... product is filtered, washed, and dried. The pigment consists principally of ferric ammonium...

  11. 21 CFR 73.1298 - Ferric ammonium ferrocyanide.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...) Identity. (1) The color additive ferric ammonium ferrocyanide is the blue pigment obtained by oxidizing... product is filtered, washed, and dried. The pigment consists principally of ferric ammonium...

  12. Ammonium Hydrosulfide: Coloring Jupiter's Clouds

    NASA Astrophysics Data System (ADS)

    Loeffler, Mark J.; Hudson, Reggie L.; Chanover, Nancy J.; Simon, Amy A.

    2015-11-01

    The appearance and composition of Jupiter’s Great Red Spot (GRS) have been studied for over a century, yet there still is no consensus for what is causing the GRS’s color. As the GRS is believed to originate in tropospheric clouds, it seems likely that one or more cloud components may contribute to the GRS's color. Recently, we have begun to investigate whether either ammonium hydrosulfide (NH4SH), a predicted cloud component, or its radiation-chemical products can produce color and/or an ultraviolet-visible spectrum similar to what has been observed on Jupiter via remote sensing (e.g., Simon et al., 2015). Our initial experiments relied on infrared spectroscopy to quantify the radiolytic and thermal stability of NH4SH and to identify the new chemical products formed during MeV ion irradiation (Loeffler et al., 2015). This DPS presentation will cover some of our most recent results detailing the ultraviolet-visible spectral and color changes observed during irradiation and post-irradiation warming of NH4SH ices. This work is funded by NASA’s Outer Planets and Planetary Atmospheres programs.

  13. Phase diagram of ammonium nitrate

    SciTech Connect

    Dunuwille, Mihindra; Yoo, Choong-Shik

    2013-12-07

    Ammonium Nitrate (AN) is a fertilizer, yet becomes an explosive upon a small addition of chemical impurities. The origin of enhanced chemical sensitivity in impure AN (or AN mixtures) is not well understood, posing significant safety issues in using AN even today. To remedy the situation, we have carried out an extensive study to investigate the phase stability of AN and its mixtures with hexane (ANFO–AN mixed with fuel oil) and Aluminum (Ammonal) at high pressures and temperatures, using diamond anvil cells (DAC) and micro-Raman spectroscopy. The results indicate that pure AN decomposes to N{sub 2}, N{sub 2}O, and H{sub 2}O at the onset of the melt, whereas the mixtures, ANFO and Ammonal, decompose at substantially lower temperatures. The present results also confirm the recently proposed phase IV-IV{sup ′} transition above 17 GPa and provide new constraints for the melting and phase diagram of AN to 40 GPa and 400°C.

  14. Structural and optical characterization of metal tungstates (MWO4; M=Ni, Ba, Bi) synthesized by a sucrose-templated method

    PubMed Central

    2013-01-01

    Background Metal tungstates have attracted much attention due to their interesting structural and photoluminescence properties. Depending on the size of the bivalent cation present, the metal tungstates will adopt structures with different phases. In this work, three different phases of metal tungstates MWO4 (M= Ba, Ni and Bi) were synthesized via the sucrose templated method. Results The powders of BaWO4 (tetragonal), NiWO4 (monoclinic) and Bi2WO6 (orthorhombic) formed after calcination temperatures of 750, 650 and 600°C for 4 h respectively are found to be crystalline and exist in their pure phase. Based on Scherrer estimation, their crystallite size are of nanosized. BET results showed NiWO4 has the highest surface area. BaWO4 exhibited less Raman vibrations than the NiWO4 because of the increased lattice symmetry but Bi2WO6 showed almost the same Raman vibrations as BaWO4. From the UV-vis spectra, the band gap transition of the metal tungstates are of the order of BaWO4 > Bi2WO6 > NiWO4. Broad blue-green emission peaks were detected in photoluminescence spectra and the results showed the great dependence on morphology, crystallinity and size of the metal tungstates. Conclusion Three different phases of metal tungstates of BaWO4 (scheelite), NiWO4 (wolframite) and Bi2WO6 (perovskite layer) in their pure phase were successfully prepared by the simple and economical sucrose-templated method. The highest surface area is exhibited by NiWO4 while largest band gap is shown by BaWO4. These materials showed promising optical properties. PMID:23634962

  15. Acrylonitrile butadiene rubber (NBR)/manganous tungstate (MnWO4) nanocomposites: Characterization, mechanical and electrical properties

    NASA Astrophysics Data System (ADS)

    Ramesan, M. T.; Abdu Raheem V., P.; Jayakrishnan, P.; Pradyumnan, P. P.

    2014-10-01

    Nanocomposites of NBR with manganous-tungstate nanoparticles were prepared through vulcanization process. The extent of interaction of nanoparticles with the polymer was studied by FTIR, SEM, XRD, TGA and AC conductivity. FTIR and XRD ascertain the interaction of NBR with MnWO4 nanoparticles. SEM analysis established that the nanopartilces were well dispersed in the macromolecular chain of NBR. The mechanical properties of the nanocomposites were studied as a function of filler loading. The nanocomposites exhibited enhanced thermal stability as seen in TGA. Conductivity and dielectric properties of nanocomposites increase with increase in concentration of MnWO4 nanoparticles (7phr) and thereafter the value decreases.

  16. Sarcoplasmic reticulum calcium ATPase interactions with decaniobate, decavanadate, vanadate, tungstate and molybdate.

    PubMed

    Fraqueza, Gil; Ohlin, C André; Casey, William H; Aureliano, Manuel

    2012-02-01

    Over the last few decades there has been increasing interest in oxometalate and polyoxometalate applications to medicine and pharmacology. This interest arose, at least in part, due to the properties of these classes of compounds as anti-cancer, anti-diabetic agents, and also for treatment of neurodegenerative diseases, among others. However, our understanding of the mechanism of action would be improved if biological models could be used to clarify potential toxicological effects in main cellular processes. Sarcoplasmic reticulum (SR) vesicles, containing a large amount of Ca(2+)-ATPase, an enzyme that accumulates calcium by active transport using ATP, have been suggested as a useful model to study the effects of oxometalates on calcium homeostasis. In the present article, it is shown that decavanadate, decaniobate, vanadate, tungstate and molybdate, all inhibited SR Ca(2+)-ATPase, with the following IC(50) values: 15, 35, 50, 400 μM and 45 mM, respectively. Decaniobate (Nb(10)), is the strongest P-type enzyme inhibitor, after decavanadate (V(10)). Atomic-absorption spectroscopy (AAS) analysis, indicates that decavanadate binds to the protein with a 1:1 decavanadate:Ca(2+)-ATPase stoichiometry. Furthermore, V(10) binds with similar extension to all the protein conformations, which occur during calcium translocation by active transport, namely E1, E1P, E2 and E2P, as analysed by AAS. In contrast, it was confirmed that the binding of monomeric vanadate (H(2)VO(4)(2-); V(1)) to the calcium pump is favoured only for the E2 and E2P conformations of the ATPase, whereas no significant amount of vanadate is bound to the E1 and E1P conformations. Scatchard plot analysis, confirmed a 1:1 ratio for decavanadate-Ca(2+)-ATPase, with a dissociation constant, k(d) of 1 μM(-1). The interaction of decavanadate V(10)O(28)(6-) (V(10)) with Ca(2+)-ATPase is prevented by the isostructural and isoelectronic decaniobate Nb(10)O(28)(6-) (Nb(10)), whereas no significant effects were

  17. Cation–cation interactions and cation exchange in a series of isostructural framework uranyl tungstates

    SciTech Connect

    Balboni, Enrica; Burns, Peter C.

    2014-05-01

    treatments. The framework of these compounds is robust to cation exchange and heat. (yellow polyhedra=uranium pentagonal bipyramids; blue polyhedra=tungsten octahedral, purple balls=K; yellow balls=Na; grey balls=Tl). - Highlights: • Five isostructural uranyl tungstates compounds were synthesized hydrothermally. • The structures consist of a chains of uranium and tungstate polyhedral. • Chains are connected into a framework by cation–cation interactions. • Cation exchange does not alter the structural integrity of the compounds. • Cation exchange was successful at room temperature and mild hydrothermal conditions.

  18. Structural, microstructural and vibrational analyses of the monoclinic tungstate BiLuWO{sub 6}

    SciTech Connect

    Ait Ahsaine, H.; Taoufyq, A.; Patout, L.; Ezahri, M.; Benlhachemi, A.; Bakiz, B.; Villain, S.; Guinneton, F.; Gavarri, J.-R.

    2014-10-15

    The bismuth lutetium tungstate phase BiLuWO{sub 6} has been prepared using a solid state route with stoichiometric mixtures of oxide precursors. The obtained polycrystalline phase has been characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Raman spectroscopy. In the first step, the crystal structure has been refined using Rietveld method: the crystal cell was resolved using monoclinic system (parameters a, b, c, β) with space group A2/m. SEM images showed the presence of large crystallites with a constant local nominal composition (BiLuW). TEM analyses showed that the actual local structure could be better represented by a superlattice (a, 2b, c, β) associated with space groups P2 or P2/m. The Raman spectroscopy showed the presence of vibrational bands similar to those observed in the compounds BiREWO{sub 6} with RE=Y, Gd, Nd. However, these vibrational bands were characterized by large full width at half maximum, probably resulting from the long range Bi/Lu disorder and local WO{sub 6} octahedron distortions in the structure. - Graphical abstract: The average structure of BiLuWO{sub 6} determined from X-ray diffraction data can be represented by A2/m space group. Experimental Electron Diffraction patterns along the [0vw] zone axes of the monoclinic structure and associated simulated patterns show the existence of a monoclinic superstructure with space group P2 or P2/m. - Highlights: • A new monoclinic BiLuWO{sub 6} phase has been elaborated from solid-state reaction. • The space group of the monoclinic disordered average structure should be A2/m. • Transmission electron microscopy leads to a superlattice with P2/m space group. • Raman spectroscopy suggests existence of local disorder.

  19. In-situ growth of zinc tungstate nanorods on graphene for enhanced photocatalytic performance

    SciTech Connect

    Rao, Lei; Xu, Junling; Ao, Yanhui; Wang, Peifang

    2014-09-15

    Graphical abstract: Graphene/ZnWO{sub 4} (G–ZnWO{sub 4}) nanorod composite photocatalysts were prepared by a simple one-step method. Namely, the reduction of graphene oxide and the growth of ZnWO{sub 4} nanorod occurred simultaneously in one single process. An enhancement in the photocatalytic activities were observed in G–ZnWO{sub 4} composites compared with pure ZnWO{sub 4} under UV light irradiation. - Highlights: • Graphene–ZnWO{sub 4} composite photocatalyst was prepared for the first time. • The as-prepared composite photocatalysts show high activity for dye degradation. • Effect of graphene amount on the photocatalytic activity was investigated. - Abstract: Graphene–zinc tungstate (G–ZnWO{sub 4}) hybrid photocatalysts were prepared by an in-situ growth method in which the reduction of graphene oxide (GO) and the growth of ZnWO{sub 4} crystals occurred simultaneously. The materials were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, UV–vis diffuse reflectance spectroscopy and X-ray photoelectron spectroscopy. The photocatalytic activity was investigated by the degradation of dye methylene blue (MB). An enhancement in the photocatalytic activity was observed for G–ZnWO{sub 4} hybrids compared with pure ZnWO{sub 4} under UV light. This improvement was attributed to the following two reasons: increased migration efficiency of photo-induced electrons and increased adsorption activity for dye molecules. The effect of the amount of graphene on the photocatalytic activity was also investigated. Results showed that there was an optimum amount of 2%.

  20. In-situ non-ambient X-ray diffraction studies of indium tungstate

    SciTech Connect

    Baiz, Tamam I.; Heinrich, Christophe P.; Banek, Nathan A.; Vivekens, Boris L.; Lind, Cora

    2012-03-15

    In situ variable temperature and high pressure X-ray diffraction studies were carried out on indium tungstate (In{sub 2}W{sub 3}O{sub 12}). This material displays positive volume expansion in both its low temperature monoclinic and high temperature orthorhombic phases, with negative thermal expansion along the a axis and positive thermal expansion along the b and c axes. Upon hydrostatic compression in a diamond anvil cell, one crystalline to crystalline phase transition is observed in the range 1.9 to 2.7 GPa, and progressive irreversible amorphization occurs at pressures above 4.3 GPa. The crystalline high pressure phase appears to be isostructural to previously observed high pressure phases in other A{sub 2}M{sub 3}O{sub 12} compounds. - Graphical abstract: Variable pressure X-ray diffraction patterns of In{sub 2}W{sub 3}O{sub 12} collected in a diamond anvil cell. A phase transition is clearly observed between 2.2 and 2.7 GPa, followed by irreversible amorphization. Highlights: Black-Right-Pointing-Pointer The structure of In{sub 2}W{sub 3}O{sub 12} was studied as a function of temperature and pressure. Black-Right-Pointing-Pointer Uniaxial negative thermal expansion was observed above 250 Degree-Sign C. Black-Right-Pointing-Pointer A pressure-induced phase transition occurred between 2.2 and 2.7 GPa. Black-Right-Pointing-Pointer Pressure-induced irreversible amorphization was observed above 4.3 GPa.

  1. redox reactions of uranium in the presence of potassium 2-phospho-17-tungstate

    SciTech Connect

    Maslov, L.P.; Rykov, A.G.; Sirotinkina, L.V.

    1986-07-01

    The redox reactions of uranium in the presence of potassium 2-phospho-17-tungstate (17W2P) - K/sub 10/P/sub 2/W/sub 17/O/sub 61/ - were studied by the methods of spectrophotometry and potentiometry. It was established that in the presence of 17W2P the UO /SUP 2/2/ /sup +/ ion is reduced by iron(II) to uranium(IV) as a result of the binding of U(IV) into a strong complex with composition (U(p/sub 2/W/sub 17/O/sub 61/)/sub 2/)/sup 16 -/. The peculiarities of the coordination of uranium(IV) by voluminous 17W2P ligands are the cause of the different nature of its interaction with various types of oxidizing agents. It was established that under the action of oxidizing agents (K/sub 2/Cr/sub 2/O/sub 7/, KMnO/sub 4/), the reduced form of which is a complex with 17W2P, there is a conversion of the complex of uranium(IV) to the corresponding complex of uranium(V), evidently with conservation of a structure analogous to that for uranium(IV). It was also shown that uranium(IV) in complex with 17W2P is practically not oxidized in the cold by persulfate ions which react according to a radical mechanism, whereas weaker oxidizing agents, for example, H/sub 2/O/sub 2/, oxidize it to the UO /SUP 2/2/ /sup +/ ion. Hypotheses are advanced on the possible mechanisms of the occurrence of the corresponding reactions.

  2. Biodegradation of rocket propellent waste, ammonium perchlorate

    NASA Technical Reports Server (NTRS)

    Naqui, S. M. Z.

    1975-01-01

    The impact of the biodegradation rate of ammonium perchlorate on the environment was studied in terms of growth, metabolic rate, and total biomass of selected animal and plant species. Brief methodology and detailed results are presented.

  3. Electrochemically and bioelectrochemically induced ammonium recovery.

    PubMed

    Gildemyn, Sylvia; Luther, Amanda K; Andersen, Stephen J; Desloover, Joachim; Rabaey, Korneel

    2015-01-01

    Streams such as urine and manure can contain high levels of ammonium, which could be recovered for reuse in agriculture or chemistry. The extraction of ammonium from an ammonium-rich stream is demonstrated using an electrochemical and a bioelectrochemical system. Both systems are controlled by a potentiostat to either fix the current (for the electrochemical cell) or fix the potential of the working electrode (for the bioelectrochemical cell). In the bioelectrochemical cell, electroactive bacteria catalyze the anodic reaction, whereas in the electrochemical cell the potentiostat applies a higher voltage to produce a current. The current and consequent restoration of the charge balance across the cell allow the transport of cations, such as ammonium, across a cation exchange membrane from the anolyte to the catholyte. The high pH of the catholyte leads to formation of ammonia, which can be stripped from the medium and captured in an acid solution, thus enabling the recovery of a valuable nutrient. The flux of ammonium across the membrane is characterized at different anolyte ammonium concentrations and currents for both the abiotic and biotic reactor systems. Both systems are compared based on current and removal efficiencies for ammonium, as well as the energy input required to drive ammonium transfer across the cation exchange membrane. Finally, a comparative analysis considering key aspects such as reliability, electrode cost, and rate is made. This video article and protocol provide the necessary information to conduct electrochemical and bioelectrochemical ammonia recovery experiments. The reactor setup for the two cases is explained, as well as the reactor operation. We elaborate on data analysis for both reactor types and on the advantages and disadvantages of bioelectrochemical and electrochemical systems. PMID:25651406

  4. 21 CFR 172.430 - Iron ammonium citrate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Iron ammonium citrate. 172.430 Section 172.430... CONSUMPTION Anticaking Agents § 172.430 Iron ammonium citrate. Iron ammonium citrate may be safely used in... human consumption so that the level of iron ammonium citrate does not exceed 25 parts per million...

  5. 21 CFR 573.560 - Iron ammonium citrate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Iron ammonium citrate. 573.560 Section 573.560... Additive Listing § 573.560 Iron ammonium citrate. Iron ammonium citrate may be safely used in animal feed... consumption so that the level of iron ammonium citrate does not exceed 25 parts per million (0.0025...

  6. 21 CFR 172.430 - Iron ammonium citrate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Iron ammonium citrate. 172.430 Section 172.430... CONSUMPTION Anticaking Agents § 172.430 Iron ammonium citrate. Iron ammonium citrate may be safely used in... human consumption so that the level of iron ammonium citrate does not exceed 25 parts per million...

  7. 21 CFR 573.560 - Iron ammonium citrate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Iron ammonium citrate. 573.560 Section 573.560... Additive Listing § 573.560 Iron ammonium citrate. Iron ammonium citrate may be safely used in animal feed... consumption so that the level of iron ammonium citrate does not exceed 25 parts per million (0.0025...

  8. 21 CFR 573.560 - Iron ammonium citrate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Iron ammonium citrate. 573.560 Section 573.560... Additive Listing § 573.560 Iron ammonium citrate. Iron ammonium citrate may be safely used in animal feed... consumption so that the level of iron ammonium citrate does not exceed 25 parts per million (0.0025...

  9. 21 CFR 573.560 - Iron ammonium citrate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Iron ammonium citrate. 573.560 Section 573.560... Additive Listing § 573.560 Iron ammonium citrate. Iron ammonium citrate may be safely used in animal feed... consumption so that the level of iron ammonium citrate does not exceed 25 parts per million (0.0025...

  10. 21 CFR 172.430 - Iron ammonium citrate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Iron ammonium citrate. 172.430 Section 172.430 Food... Anticaking Agents § 172.430 Iron ammonium citrate. Iron ammonium citrate may be safely used in food in... consumption so that the level of iron ammonium citrate does not exceed 25 parts per million (0.0025...

  11. 21 CFR 172.430 - Iron ammonium citrate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Iron ammonium citrate. 172.430 Section 172.430... CONSUMPTION Anticaking Agents § 172.430 Iron ammonium citrate. Iron ammonium citrate may be safely used in... human consumption so that the level of iron ammonium citrate does not exceed 25 parts per million...

  12. 21 CFR 573.560 - Iron ammonium citrate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Iron ammonium citrate. 573.560 Section 573.560... Additive Listing § 573.560 Iron ammonium citrate. Iron ammonium citrate may be safely used in animal feed... consumption so that the level of iron ammonium citrate does not exceed 25 parts per million (0.0025...

  13. Selection and preliminary evaluation of three structures as potential solid conductors of alkali ions: Two hollandites, a titanate, and a tungstate

    NASA Technical Reports Server (NTRS)

    Singer, J.; Kautz, H. E.; Fielder, W. L.; Fordyce, J. S.

    1973-01-01

    Utilization of crystal-chemical criteria has suggested three structure types in which alkali ions may be mobile: (1)hollandites K(x)Mg(x/2)Ti(8-x/2)O16 and K(x)Al(x)Ti(8-x)O16 for 1.6 less than or equal to x less than or equal to 2.0 tungstate K2W4013; and (3) sodium hexatitante Na2Ti6O13. Each is a tunnel structure. An electrical screening procedure, previously tested on beta-alumina, has indicated high K(+) ion mobility in the hollandites and in the tungstate, but not in the hexatitanate. Specimens were polycrystalline disks near 90 percent of theoretical density. The ac conductivity calculated from dielectric and capacitance measurements has been attributed to ion mobility. This ac conductivity was up to 0.01/ohm-cm for hollandites and about 0.0001/ohm-cm for the tungstate, with approximate activation energies of 21 to 25 and 16 kJ/mole (5 to 6 and 4 kcal/mole), respectively. Electronic conduction and chemical reactivity have eliminated the tungstate from further consideration. The hollandites have been considered worthy of further development and evaluation.

  14. Novel Inducers of the Envelope Stress Response BaeSR in Salmonella Typhimurium: BaeR Is Critically Required for Tungstate Waste Disposal

    PubMed Central

    Appia-Ayme, Corinne; Patrick, Elaine; J. Sullivan, Matthew; Alston, Mark J.; Field, Sarah J.; AbuOun, Manal; Anjum, Muna F.; Rowley, Gary

    2011-01-01

    The RpoE and CpxR regulated envelope stress responses are extremely important for SalmonellaTyphimurium to cause infection in a range of hosts. Until now the role for BaeSR in both the Salmonella Typhimurium response to stress and its contribution to infection have not been fully elucidated. Here we demonstrate stationary phase growth, iron and sodium tungstate as novel inducers of the BaeRregulon, with BaeR critically required for Salmonella resistance to sodium tungstate. We show that functional overlap between the resistance nodulation-cell division (RND) multidrug transporters, MdtA, AcrD and AcrB exists for the waste disposal of tungstate from the cell. We also point to a role for enterobactinsiderophores in the protection of enteric organisms from tungstate, akin to the scenario in nitrogen fixing bacteria. Surprisingly, BaeR is the first envelope stress response pathway investigated in S. Typhimurium that is not required for murine typhoid in either ityS or ityR mouse backgrounds. BaeR is therefore either required for survival in larger mammals such as pigs or calves, an avian host such as chickens, or survival out with the host altogether where Salmonella and related enterics must survive in soil and water. PMID:21886814

  15. Calcium sulphate in ammonium sulphate solution

    USGS Publications Warehouse

    Sullivan, E.C.

    1905-01-01

    Calcium sulphate, at 25?? C., is two-thirds as soluble in dilute (o.i mol per liter) and twice as soluble in concentrated (3 mois per liter) ammonium sulphate solution as in water. The specific electric conductivity of concentrated ammonium sulphate solutions is lessened by saturating with calcium sulphate. Assuming that dissociation of ammonium sulphate takes place into 2NH4?? and SO4" and of calcium sulphate into Ca and SO4" only, and that the conductivity is a measure of such dissociation, the solubility of calcium sulphate in dilute ammonium sulphate solutions is greater than required by the mass-law. The conductivity of the dilute mixtures may be accurately calculated by means of Arrhenius' principle of isohydric solutions. In the data obtained in these calculations, the concentration of non-dissociated calcium sulphate decreases with increasing ammonium sulphate. The work as a whole is additional evidence of the fact that we are not yet in possession of all the factors necessary for reconciling the mass-law to the behavior of electrolytes. The measurements above described were made in the chemical laboratory of the University of Michigan.

  16. Benchmark binding energies of ammonium and alkyl-ammonium ions interacting with water. Are ammonium-water hydrogen bonds strong?

    NASA Astrophysics Data System (ADS)

    Vallet, Valérie; Masella, Michel

    2015-01-01

    Alkyl-ammonium ion/water interactions are investigated using high level quantum computations, yielding thermodynamics data in good agreement with gas-phase experiments. Alkylation and hydration lead to weaken the NHsbnd O hydrogen bonds. Upon complete hydration by four water molecules, their main features are close to those of the OHsbnd O bond in the isolated water dimer. Energy decomposition analyses indicate that hydration of alkyl-ammonium ions are mainly due to electrostatic/polarization effects, as for hard monoatomic cations, but with a larger effect of dispersion.

  17. On the evaporation of ammonium sulfate solution

    PubMed Central

    Drisdell, Walter S.; Saykally, Richard J.; Cohen, Ronald C.

    2009-01-01

    Aqueous evaporation and condensation kinetics are poorly understood, and uncertainties in their rates affect predictions of cloud behavior and therefore climate. We measured the cooling rate of 3 M ammonium sulfate droplets undergoing free evaporation via Raman thermometry. Analysis of the measurements yields a value of 0.58 ± 0.05 for the evaporation coefficient, identical to that previously determined for pure water. These results imply that subsaturated aqueous ammonium sulfate, which is the most abundant inorganic component of atmospheric aerosol, does not affect the vapor–liquid exchange mechanism for cloud droplets, despite reducing the saturation vapor pressure of water significantly. PMID:19861551

  18. On the effective ionic radii for ammonium.

    PubMed

    Sidey, Vasyl

    2016-08-01

    A set of effective ionic radii corresponding to different coordination numbers (CNs) and compatible with the radii system by Shannon [Acta Cryst. (1976), A32, 751-767] has been derived for ammonium: 1.40 Å (CN = IV), 1.48 Å (CN = VI), 1.54 Å (CN = VIII) and 1.67 Å (CN = XII). The bond-valence parameters r0 = 2.3433 Å and B = 0.262 Å have been determined for ammonium-fluorine bonds. PMID:27484382

  19. On the evaporation of ammonium sulfate solution

    SciTech Connect

    Drisdell, Walter S.; Saykally, Richard J.; Cohen, Ronald C.

    2009-07-16

    Aqueous evaporation and condensation kinetics are poorly understood, and uncertainties in their rates affect predictions of cloud behavior and therefore climate. We measured the cooling rate of 3 M ammonium sulfate droplets undergoing free evaporation via Raman thermometry. Analysis of the measurements yields a value of 0.58 {+-} 0.05 for the evaporation coefficient, identical to that previously determined for pure water. These results imply that subsaturated aqueous ammonium sulfate, which is the most abundant inorganic component of atmospheric aerosol, does not affect the vapor-liquid exchange mechanism for cloud droplets, despite reducing the saturation vapor pressure of water significantly.

  20. Biospeciation of tungsten in the serum of diabetic and healthy rats treated with the antidiabetic agent sodium tungstate.

    PubMed

    Gómez-Gómez, M Milagros; Rodríguez-Fariñas, Nuria; Cañas-Montalvo, Benito; Domínguez, Jorge; Guinovart, Joan; Cámara-Rica, Carmen

    2011-05-30

    It is known that oral administration of sodium tungstate preserves the pancreatic beta cell function in diabetic rats. Healthy and streptozotocin-induced diabetic rats were treated with sodium tungstate for one, three or six weeks, after which the species of W in serum, were analysed. An increase in serum W with treatment time was observed. After six weeks, the serum W concentration in diabetic rats (70 mg L(-1)) was about 4.6 times higher than in healthy specimens. This different behaviour was also observed for Cu accumulation, while the Zn pattern follows the contrary. The patterns observed in the retention of Cu and Zn may be attributable to a normalization of glycaemia. The speciation analysis of W was performed using 2D separations, including an immunoaffinity packing and a SEC (Size Exclusion Chromatography) column coupled to an ICP-MS (Inductively Coupled Plasma Mass Spectrometry) for elemental detection. Ultrafiltration data together with SEC-ICP-MS results proved that around 80% of serum W was bound to proteins, the diabetic rats registering a higher W content than their healthy counterparts. Most of the protein-bound W was due to a complex with albumin. An unknown protein with a molecular weight higher than 100 kDa was also found to bind a small amount of W (about 2%). MALDI-TOF (Matrix-Assisted Laser Desorption Ionization Time-of-Flight) analysis of the desalted and concentrated chromatographic fractions confirmed albumin as the main protein bound to tungstate in rat serum, while no binding to transferrin (Tf) was detected. The interaction between glutathione and W was also evaluated using standard solutions; however, the formation of complexes was not observed. The stability of the complexes between W and proteins when subjected to more stringent procedures, like those used in proteomic methodologies (denaturing with urea or SDS, boiling, sonication, acid media, reduction with β-mercaptoethanol (BME) or DTT (dithiotreitol) and alkylation with

  1. Specific recognition of guanines in non-duplex regions of nucleic acids with potassium tungstate and hydrogen peroxide

    PubMed Central

    Mao, Wuxiang; Xu, Xiaowei; He, Huan; Huang, Rong; Chen, Xi; Xiao, Heng; Yu, Zhenduo; Liu, Yi; Zhou, Xiang

    2015-01-01

    Structural features of nucleic acids have become an integral part of current biomedical research. Highly selective and readily performed methods with little toxicity that target guanosines in non-duplex nucleic acids are needed, which led us to search for an effective agent for guanosine sequencing. Treatment of DNA or RNA with potassium tungstate and hydrogen peroxide produced damaged guanosines in DNA or RNA sequences. The damaged guanosines in non-duplex DNA could be cleaved by hot piperidine. Similarly, damaged guanosines in non-duplex RNA could be cleaved by aniline acetate. We could identify structural features of nucleic acid using this strategy instead of dimethyl sulphate and Ribonuclease T1. PMID:25355517

  2. 21 CFR 184.1133 - Ammonium alginate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...: Category of food Maximum level of use in food (as served) (percent) Functional use Confections, frostings... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ammonium alginate. 184.1133 Section 184.1133 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD...

  3. 21 CFR 184.1133 - Ammonium alginate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ammonium alginate. 184.1133 Section 184.1133 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of Specific Substances Affirmed as GRAS...

  4. 21 CFR 582.1137 - Ammonium carbonate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Ammonium carbonate. 582.1137 Section 582.1137 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...

  5. 21 CFR 582.1135 - Ammonium bicarbonate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Ammonium bicarbonate. 582.1135 Section 582.1135 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...

  6. 21 CFR 582.1137 - Ammonium carbonate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Ammonium carbonate. 582.1137 Section 582.1137 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...

  7. 21 CFR 582.1135 - Ammonium bicarbonate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Ammonium bicarbonate. 582.1135 Section 582.1135 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...

  8. 21 CFR 582.1139 - Ammonium hydroxide.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Ammonium hydroxide. 582.1139 Section 582.1139 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...

  9. 21 CFR 582.1139 - Ammonium hydroxide.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Ammonium hydroxide. 582.1139 Section 582.1139 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...

  10. 21 CFR 582.1137 - Ammonium carbonate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Ammonium carbonate. 582.1137 Section 582.1137 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...

  11. 21 CFR 582.1139 - Ammonium hydroxide.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Ammonium hydroxide. 582.1139 Section 582.1139 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...

  12. 21 CFR 582.1135 - Ammonium bicarbonate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Ammonium bicarbonate. 582.1135 Section 582.1135 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...

  13. Diamond Head Revisited with Ammonium Dichromate.

    ERIC Educational Resources Information Center

    Arrigoni, Edward

    1981-01-01

    The classroom demonstration using ammonium dichromate to simulate a volcanic eruption can be modified into a more dramatic and accurate representation of the geologic processes involved in the formation of a volcanic crater. The materials, demonstration setup, safety procedures, and applications to instruction are presented. (Author/WB)

  14. Near infrared detection of ammonium minerals.

    USGS Publications Warehouse

    Krohn, M.D.; Altaner, S.P.

    1987-01-01

    Diagnostic near-infrared spectral features have been identified for minerals with ammonium (NH4+) bound in the crystal structure. Near-infrared detection of NH4-bearing minerals may provide useful information for prospecting for certain ore deposits and may provide a better understanding of the nitrogen cycle within geologic environments.-from Authors

  15. 21 CFR 556.375 - Maduramicin ammonium.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Maduramicin ammonium. 556.375 Section 556.375 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS TOLERANCES FOR RESIDUES OF NEW ANIMAL DRUGS IN FOOD Specific Tolerances for Residues of New Animal Drugs §...

  16. 21 CFR 573.170 - Ammonium formate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...) The additive is manufactured by the reaction of 99.5 percent ammonia gas and 99 percent formic acid in...) To assure safe use of the additive, in addition to the other information required by the Federal Food... labeled as containing ammonium formate. (d) To assure safe use of the additive, in addition to the...

  17. 21 CFR 573.170 - Ammonium formate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...) The additive is manufactured by the reaction of 99.5 percent ammonia gas and 99 percent formic acid in...) To assure safe use of the additive, in addition to the other information required by the Federal Food... labeled as containing ammonium formate. (d) To assure safe use of the additive, in addition to the...

  18. 21 CFR 573.170 - Ammonium formate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... is manufactured by the reaction of 99.5 percent ammonia gas and 99 percent formic acid in a... safe use of the additive, in addition to the other information required by the Federal Food, Drug, and... ammonium formate. (d) To assure safe use of the additive, in addition to the other information required...

  19. 21 CFR 184.1137 - Ammonium carbonate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ammonium carbonate. 184.1137 Section 184.1137 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of Specific Substances Affirmed as GRAS...

  20. 21 CFR 184.1143 - Ammonium sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ammonium sulfate. 184.1143 Section 184.1143 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of Specific Substances Affirmed as GRAS...

  1. 21 CFR 184.1137 - Ammonium carbonate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ammonium carbonate. 184.1137 Section 184.1137 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of Specific Substances Affirmed as GRAS...

  2. Cyclo­hexyl­ammonium nitrate

    PubMed Central

    Bagabas, Abdulaziz A.; Aboud, Mohamed F. A.; Shemsi, Ahsan M.; Addurihem, Emad S.; Al-Othman, Zeid A.; Chidan Kumar, C. S.; Fun, Hoong-Kun

    2014-01-01

    In the title salt, C6H14N+·NO3 −, the cyclo­hexyl ring adopts a chair conformation. The ammonium group occupies an equatorial position and the crystal struture is stabilized by inter­molecular N—H⋯O hydrogen-bonding inter­actions, resulting in a three-dimensional network. PMID:24764971

  3. 76 FR 70366 - Ammonium Nitrate Security Program

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-11-14

    ... Department previously announced a series of public meetings on the same topic on October 2, 2011 (see 76 FR... public comment on August 3, 2011. See 73 FR 64280 (advance notice of proposed rulemaking); 76 FR 46908... the Department's Ammonium Nitrate Security Program Web site, at...

  4. MECHANISM BY WHICH AMMONIUM FERTILIZERS KILL LARKSPUR

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Environmental concerns of using pesticides on public lands have greatly reduced the use of herbicides to control tall larkspur (Delphinium barbeyi). Alternative methods of control have used ammonium sulfate placed in the crown of individual plants to kill larkspur. The objective of this study was ...

  5. 76 FR 47238 - Ammonium Nitrate From Russia

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-04

    ...)). Background The Commission instituted this review on March 1, 2011 (76 FR 11273) and determined on June 6, 2011 that it would conduct an expedited review (76 FR 34749, June 14, 2011). The Commission transmitted... COMMISSION Ammonium Nitrate From Russia Determination On the basis of the record \\1\\ developed in the...

  6. 21 CFR 573.170 - Ammonium formate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...) The additive is manufactured by the reaction of 99.5 percent ammonia gas and 99 percent formic acid in a continuous loop reactor to produce a solution made up of 37 percent ammonium salt of formic acid and 62 percent formic acid. (b) The additive is used or intended for use as a feed acidifying...

  7. 21 CFR 184.1139 - Ammonium hydroxide.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... specifications of the Food Chemicals Codex, 3d Ed. (1981), p. 20, which is incorporated by reference. Copies are... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ammonium hydroxide. 184.1139 Section 184.1139 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD...

  8. 21 CFR 184.1135 - Ammonium bicarbonate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... ingredient meets the specifications of the Food Chemicals Codex, 3d Ed. (1981), p. 19, which is incorporated... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ammonium bicarbonate. 184.1135 Section 184.1135 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)...

  9. 40 CFR 721.4095 - Quaternary ammonium alkyltherpropyl trialkylamine halides.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... trialkylamine halides. 721.4095 Section 721.4095 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.4095 Quaternary ammonium alkyltherpropyl trialkylamine halides. (a... generically as quaternary ammonium alkyltherpropyl trialkylamine halides (PMNs...

  10. 21 CFR 184.1296 - Ferric ammonium citrate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...) ammonium citrate, CAS Reg. No. 1332-98-5) is a complex salt of undetermined structure composed of 16.5 to... (iron (III) ammonium citrate, CAS Reg. No. 1333-00-2) is a complex salt of undetermined...

  11. 40 CFR 721.10099 - Dialkyl dimethyl ammonium carbonate (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Dialkyl dimethyl ammonium carbonate... Specific Chemical Substances § 721.10099 Dialkyl dimethyl ammonium carbonate (generic). (a) Chemical... as dialkyl dimethyl ammonium carbonate (1:1) (PMN P-03-715) is subject to reporting under...

  12. 40 CFR 721.10302 - Zinc ammonium phosphate (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Zinc ammonium phosphate (generic). 721... Substances § 721.10302 Zinc ammonium phosphate (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as zinc ammonium phosphate (PMN...

  13. 40 CFR 721.10302 - Zinc ammonium phosphate (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Zinc ammonium phosphate (generic). 721... Substances § 721.10302 Zinc ammonium phosphate (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as zinc ammonium phosphate (PMN...

  14. 40 CFR 721.10302 - Zinc ammonium phosphate (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Zinc ammonium phosphate (generic). 721... Substances § 721.10302 Zinc ammonium phosphate (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as zinc ammonium phosphate (PMN...

  15. 40 CFR 721.10591 - Tertiary ammonium compound (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Tertiary ammonium compound (generic... Specific Chemical Substances § 721.10591 Tertiary ammonium compound (generic). (a) Chemical substance and... ammonium compound (PMN P-11-110) is subject to reporting under this section for the significant new...

  16. 40 CFR 721.10591 - Tertiary ammonium compound (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Tertiary ammonium compound (generic... Specific Chemical Substances § 721.10591 Tertiary ammonium compound (generic). (a) Chemical substance and... ammonium compound (PMN P-11-110) is subject to reporting under this section for the significant new...

  17. 40 CFR 721.10582 - Quaternary ammonium compound (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Quaternary ammonium compound (generic... Specific Chemical Substances § 721.10582 Quaternary ammonium compound (generic). (a) Chemical substance and... ammonium compound (PMN P-10-571) is subject to reporting under this section for the significant new...

  18. 40 CFR 721.10582 - Quaternary ammonium compound (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Quaternary ammonium compound (generic... Specific Chemical Substances § 721.10582 Quaternary ammonium compound (generic). (a) Chemical substance and... ammonium compound (PMN P-10-571) is subject to reporting under this section for the significant new...

  19. 21 CFR 184.1141a - Ammonium phosphate, monobasic.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ammonium phosphate, monobasic. 184.1141a Section... SAFE Listing of Specific Substances Affirmed as GRAS § 184.1141a Ammonium phosphate, monobasic. (a) Ammonium phosphate, monobasic (NH4H2PO4, CAS Reg. No. 7722-76-1) is manufactured by reacting ammonia...

  20. 21 CFR 184.1141a - Ammonium phosphate, monobasic.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ammonium phosphate, monobasic. 184.1141a Section... SAFE Listing of Specific Substances Affirmed as GRAS § 184.1141a Ammonium phosphate, monobasic. (a) Ammonium phosphate, monobasic (NH4H2PO4, CAS Reg. No. 7722-76-1) is manufactured by reacting ammonia...

  1. 21 CFR 582.1127 - Aluminum ammonium sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Aluminum ammonium sulfate. 582.1127 Section 582.1127 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED... Additives § 582.1127 Aluminum ammonium sulfate. (a) Product. Aluminum ammonium sulfate. (b) Conditions...

  2. 21 CFR 182.1127 - Aluminum ammonium sulfate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Aluminum ammonium sulfate. 182.1127 Section 182.1127 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED... Food Substances § 182.1127 Aluminum ammonium sulfate. (a) Product. Aluminum ammonium sulfate....

  3. 21 CFR 582.1127 - Aluminum ammonium sulfate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Aluminum ammonium sulfate. 582.1127 Section 582.1127 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED... Additives § 582.1127 Aluminum ammonium sulfate. (a) Product. Aluminum ammonium sulfate. (b) Conditions...

  4. 21 CFR 182.1127 - Aluminum ammonium sulfate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Aluminum ammonium sulfate. 182.1127 Section 182.1127 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED... Food Substances § 182.1127 Aluminum ammonium sulfate. (a) Product. Aluminum ammonium sulfate....

  5. 21 CFR 582.1127 - Aluminum ammonium sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Aluminum ammonium sulfate. 582.1127 Section 582.1127 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED... Additives § 582.1127 Aluminum ammonium sulfate. (a) Product. Aluminum ammonium sulfate. (b) Conditions...

  6. 21 CFR 182.1127 - Aluminum ammonium sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Aluminum ammonium sulfate. 182.1127 Section 182.1127 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED... Food Substances § 182.1127 Aluminum ammonium sulfate. (a) Product. Aluminum ammonium sulfate....

  7. 21 CFR 182.1127 - Aluminum ammonium sulfate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Aluminum ammonium sulfate. 182.1127 Section 182...) SUBSTANCES GENERALLY RECOGNIZED AS SAFE Multiple Purpose GRAS Food Substances § 182.1127 Aluminum ammonium sulfate. (a) Product. Aluminum ammonium sulfate. (b) Conditions of use. This substance is...

  8. 21 CFR 582.1127 - Aluminum ammonium sulfate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Aluminum ammonium sulfate. 582.1127 Section 582.1127 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED... Additives § 582.1127 Aluminum ammonium sulfate. (a) Product. Aluminum ammonium sulfate. (b) Conditions...

  9. 21 CFR 582.1127 - Aluminum ammonium sulfate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Aluminum ammonium sulfate. 582.1127 Section 582.1127 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED... Additives § 582.1127 Aluminum ammonium sulfate. (a) Product. Aluminum ammonium sulfate. (b) Conditions...

  10. 21 CFR 182.1127 - Aluminum ammonium sulfate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Aluminum ammonium sulfate. 182.1127 Section 182.1127 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED... Food Substances § 182.1127 Aluminum ammonium sulfate. (a) Product. Aluminum ammonium sulfate....

  11. 21 CFR 73.1025 - Ferric ammonium citrate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 1 2014-04-01 2014-04-01 false Ferric ammonium citrate. 73.1025 Section 73.1025 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Drugs § 73.1025 Ferric ammonium citrate. (a) Identity. The color additive ferric ammonium...

  12. 21 CFR 172.430 - Iron ammonium citrate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Iron ammonium citrate. 172.430 Section 172.430... ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION Anticaking Agents § 172.430 Iron ammonium citrate. Iron ammonium citrate may be safely used in food in accordance with the...

  13. 40 CFR 721.10430 - Tetra alkyl ammonium salt (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Tetra alkyl ammonium salt (generic... Specific Chemical Substances § 721.10430 Tetra alkyl ammonium salt (generic). (a) Chemical substance and... ammonium salt (PMN P-97-823) is subject to reporting under this section for the significant new...

  14. 40 CFR 721.10430 - Tetra alkyl ammonium salt (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Tetra alkyl ammonium salt (generic... Specific Chemical Substances § 721.10430 Tetra alkyl ammonium salt (generic). (a) Chemical substance and... ammonium salt (PMN P-97-823) is subject to reporting under this section for the significant new...

  15. 40 CFR 721.10511 - Quaternary ammonium salts (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Quaternary ammonium salts (generic... Specific Chemical Substances § 721.10511 Quaternary ammonium salts (generic). (a) Chemical substance and... ammonium salts (PMNs P-07-320, P-07-321, P-07-322, P-07-323, and P-07-324) are subject to reporting...

  16. 40 CFR 721.10511 - Quaternary ammonium salts (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Quaternary ammonium salts (generic... Specific Chemical Substances § 721.10511 Quaternary ammonium salts (generic). (a) Chemical substance and... ammonium salts (PMNs P-07-320, P-07-321, P-07-322, P-07-323, and P-07-324) are subject to reporting...

  17. 21 CFR 184.1141a - Ammonium phosphate, monobasic.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ammonium phosphate, monobasic. 184.1141a Section... SAFE Listing of Specific Substances Affirmed as GRAS § 184.1141a Ammonium phosphate, monobasic. (a) Ammonium phosphate, monobasic (NH4H2PO4, CAS Reg. No. 7722-76-1) is manufactured by reacting ammonia...

  18. 21 CFR 184.1141a - Ammonium phosphate, monobasic.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ammonium phosphate, monobasic. 184.1141a Section... SAFE Listing of Specific Substances Affirmed as GRAS § 184.1141a Ammonium phosphate, monobasic. (a) Ammonium phosphate, monobasic (NH4H2PO4, CAS Reg. No. 7722-76-1) is manufactured by reacting ammonia...

  19. 21 CFR 184.1141a - Ammonium phosphate, monobasic.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ammonium phosphate, monobasic. 184.1141a Section 184.1141a Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES... Affirmed as GRAS § 184.1141a Ammonium phosphate, monobasic. (a) Ammonium phosphate, monobasic...

  20. 21 CFR 184.1141b - Ammonium phosphate, dibasic.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ammonium phosphate, dibasic. 184.1141b Section 184.1141b Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED... as GRAS § 184.1141b Ammonium phosphate, dibasic. (a) Ammonium phosphate, dibasic ((NH4)2HPO4, CAS...

  1. Local pharmacological effects of tungstate on the color-pattern determination of butterfly wings: a possible relationship between the eyespot and parafocal element.

    PubMed

    Dhungel, Bidur; Otaki, Joji M

    2009-11-01

    Butterfly wing color patterns can be changed by the application of a temperature shock or pharmacological agents such as tungstate, producing a distinctive type of elemental modification called the TS (temperature shock) type. Heterochronic uncoupling between the signaling and reception steps during the color-pattern determination process has been proposed as a mechanism for TS-type changes. As an extension of this hypothesis, both the parafocal element (PFE) and the eyespot in the same wing compartment are considered to be determined by morphogenic signal(s) emitted from the same eyespot focus. However, these models need to be examined with additional experimental data. Furthermore, there is controversy as to whether the action of tungstate on wing color patterns is direct or Indirect. Using a species of nymphalid butterfly (Junonia orithya), we have devised a simple method for the local application of pharmacological agents directly on developing wings of pupae. Local tungstate application resulted in reduced eyespots and circular dislocated PFEs in the eyespot-less compartments only on the treated wing, demonstrating that tungstate directly induces color-pattern changes on wings. We further examined the eyespot-PFE relationship in normal and cold-shocked Individuals, showing that an eyespot can be superimposed on a PFE and vice versa, probably depending on the timing of their fate determination. Taken together, we propose a two-morphogen model for the normal color-pattern determination, in which the morphogenic signals for the eyespot and PFE are different from each other despite their Identical origin. This two-morphogen model is compatible with the heterochronic uncoupling model for TS-type changes. PMID:19877835

  2. Detonation Properties of Ammonium Dinitramide (ADN)

    NASA Astrophysics Data System (ADS)

    Wätterstam, A.; Östmark, H.; Helte, A.; Karlsson, S.

    1999-06-01

    Ammonium Dinitramide, ADN, has a potential as an oxidizer for underwater high explosives. Pure ADN has a large reaction-zone length and shows a strong non-ideal behaviour. The work presented here is an extension of previous work.(Sensitivity and Performance Characterization of Ammonium Dinitramide (ADN). Presented at 11th International Detonation Symposium, Snowmass, CO, 1998.) Experiments for determining the detonation velocity as a function of inverse charge radius and density, reaction-zone length and curvature, and the detonation pressure are presented. Measurements of pressure indicates that no, or weak von-Neumann spike exists, suggesting an immediate chemical decomposition. Experimental data are compared with predicted using thermochemical codes and ZND-theory.

  3. Ammonium and methylammonium transport in Rhodobacter sphaeroides

    SciTech Connect

    Cordts, M.L.

    1988-01-01

    The properties of two ammonium transport systems, including a novel NH{sub 4}{sup +}-specific system, were studied in the phototrophic bacterium Rhodobacter sphaeroides 2.4.1. The organism's ability to transport NH{sub 4}{sup +} was characterized by: (1) filtration assays of the analog, {sup 14}CH{sub 3}NH{sub 3}{sup +} and (2) comparison of extracellular and intracellular NH{sub 4}{sup +} concentrations determined chemically under various conditions. Both {sup 14}CH{sub 3}NH{sub 3}{sup +} transport and maintenance of intracellular NH{sub 4}{sup +} pools were observed when glutamine synthetase was inhibited by methionine sulfoximine, suggesting ammonium transport and assimilation occurred independently.

  4. Optical constants of concentrated aqueous ammonium sulfate.

    NASA Technical Reports Server (NTRS)

    Remsberg, E. E.

    1973-01-01

    Using experimental data obtained from applying spectroscopy to a 39-wt-% aqueous ammonium sulfate solution, it is shown that, even though specific aerosol optical constants appear quite accurate, spectral variations may exist as functions of material composition or concentration or both. Prudent users of optical constant data must then include liberal data error estimates when performing calculations or in interpreting spectroscopic surveys of collected aerosol material.

  5. Corrosion and repairs of ammonium carbamate decomposers

    SciTech Connect

    De Romero, M.F.; Galban, J.P.

    1996-05-01

    Corrosion-erosion problems occurred in the carbon steel base metal of the ammonium carbamate decomposers in an urea extraction process lined with type 316L (UNS S31603) urea grade stainless steel. The cladding was replaced by weld overlay using a semiautomatic gas metal arc welding process. The first layer was alloy 25%Cr-15%Ni-2%Mo (UNS W30923); the second layer was alloy 25%Cr-22%Ni-2%Mo (UNS W31020).

  6. PROCESS FOR THE PRODUCTION OF AMMONIUM URANIUM FLUORIDE

    DOEpatents

    Ellis, A.S.; Mooney, R.B.

    1953-08-25

    This patent relates to the preparation of ammonium uranium fluoride. The process comprises adding a water soluble fluoride to an aqueous solution of a uranous compound containing an ammonium salt, and isolating the resulting precipitate. This patent relates to the manufacture of uranium tetnafluoride from ammonium uranium fluoride, NH/sub 4/UF/sub 5/. Uranium tetrafluoride is prepared by heating the ammonium uranium fluoride to a temperature at which dissociation occurs with liberation of ammonium fluoride. Preferably the process is carried out under reduced pressure, or in a current of an inert gas.

  7. Oxidation of ammonium sulfite in aqueous solutions using ozone technology

    NASA Astrophysics Data System (ADS)

    Li, Yue; Shang, Kefeng; Lu, Na; Li, Jie; Wu, Yan

    2013-03-01

    How to deal with unstable ammonium sulfite, the byproduct of flue gas desulfuration by ammonia absorption methods, has been a difficult problem in recent years. Oxidation of ammonium sulfite in aqueous solutions using ozone produced by a surface discharge system was investigated in the paper. The oxidation efficiency of ammonium sulfite by ozone and traditional air aeration were compared, and the factors including ozone concentration, gas flow rate, initial concentration of ammonium sulfite solution and reaction temperature were discussed. The results show that the oxidation efficiency of ammonium sulfite by ozone technology reached nearly 100% under the optimum conditions, which had a significant increase compared with that by air aeration.

  8. Detection of the Ammonium Ion in Space

    NASA Astrophysics Data System (ADS)

    Cernicharo, J.; Tercero, B.; Fuente, A.; Domenech, J. L.; Cueto, M.; Carrasco, E.; Herrero, V. J.; Tanarro, I.; Marcelino, N.; Roueff, E.; Gerin, M.; Pearson, J.

    2013-07-01

    We report on the detection of a narrow feature at 262816.73 MHz toward Orion and the cold prestellar core B1-bS which we attribute to the 10-00 line of the deuterated ammonium ion, NH3D+. The observations were performed with the IRAM 30 m radio telescope. The carrier has to be a light molecular species as it is the only feature detected over 3.6 GHz of bandwidth. The hyperfine structure is not resolved, indicating a very low value for the electric quadrupolar coupling constant of nitrogen which is expected for NH3D+ as the electric field over the N nucleus is practically zero. Moreover, the feature is right at the predicted frequency for the 10-00 transition of the ammonium ion, 262817 ± 6 MHz (3σ), using rotational constants derived from new infrared data obtained in our laboratory in Madrid. The estimated column density is (1.1 ± 0.2) × 1012 cm-2. Assuming a deuterium enhancement similar to that of NH2D, we derive N(NH_4^+) ~= 2.6 × 1013 cm-2, i.e., an abundance for ammonium of a few 10-11. This work was based on observations carried out with the IRAM 30 m telescope. IRAM is supported by INSU/CNRS (France), MPG (Germany), and IGN (Spain)

  9. DETECTION OF THE AMMONIUM ION IN SPACE

    SciTech Connect

    Cernicharo, J.; Tercero, B.; Fuente, A.; Domenech, J. L.; Cueto, M.; Carrasco, E.; Herrero, V. J.; Tanarro, I.; Marcelino, N.; Roueff, E.; Gerin, M.; Pearson, J.

    2013-07-01

    We report on the detection of a narrow feature at 262816.73 MHz toward Orion and the cold prestellar core B1-bS which we attribute to the 1{sub 0}-0{sub 0} line of the deuterated ammonium ion, NH{sub 3}D{sup +}. The observations were performed with the IRAM 30 m radio telescope. The carrier has to be a light molecular species as it is the only feature detected over 3.6 GHz of bandwidth. The hyperfine structure is not resolved, indicating a very low value for the electric quadrupolar coupling constant of nitrogen which is expected for NH{sub 3}D{sup +} as the electric field over the N nucleus is practically zero. Moreover, the feature is right at the predicted frequency for the 1{sub 0}-0{sub 0} transition of the ammonium ion, 262817 {+-} 6 MHz (3{sigma}), using rotational constants derived from new infrared data obtained in our laboratory in Madrid. The estimated column density is (1.1 {+-} 0.2) Multiplication-Sign 10{sup 12} cm{sup -2}. Assuming a deuterium enhancement similar to that of NH{sub 2}D, we derive N(NH{sub 4}{sup +}) {approx_equal} 2.6 Multiplication-Sign 10{sup 13} cm{sup -2}, i.e., an abundance for ammonium of a few 10{sup -11}.

  10. Equation of State of Ammonium Nitrate

    NASA Astrophysics Data System (ADS)

    Robbins, David L.; Sheffield, Stephen A.; Dattelbaum, Dana M.; Velisavljevic, Nenad; Stahl, David B.

    2009-12-01

    Ammonium nitrate (AN) is a widely used fertilizer and mining explosive. AN is commonly used in ammonium nitrate-fuel oil (ANFO), which is a mixture of explosive-grade AN prills and fuel oil in a 94:6 ratio by weight. ANFO is a non-ideal explosive with measured detonation velocities around 4 km/s. The equation of state properties and known initiation behavior of neat AN are limited. We present the results of a series of gas gun-driven plate impact experiments on pressed neat ammonium nitrate at 1.72 g/cm3. No evidence of initiation was observed under shock loading to 22 GPa. High pressure x-ray diffraction experiments in diamond anvil cells provided insight into the high pressure phase behavior over the same pressure range (to 25 GPa), as well as a static isotherm at ambient temperature. From the isotherm and thermodynamic properties at ambient conditions, a preliminary unreacted equation of state (EOS) has been developed based on the Murnaghan isotherm and Helmholtz formalism [1], which compares favorably with the available experimental Hugoniot data on several densities of AN.

  11. Resistance of Pseudomonas to Quaternary Ammonium Compounds

    PubMed Central

    Adair, Frank W.; Geftic, Sam G.; Gelzer, Justus

    1971-01-01

    Tube dilution experiments showed that benzalkonium chloride (BC)-resistant mutants of Pseudomonas aeruginosa grown in the presence of 1,000 μg of BC per ml were at least 20 times more sensitive to polymyxin B and colistin sulfate than the BC-sensitive (BCS) parent strain. BCS cells selected for resistance to 500 μg of polymyxin B per ml remained sensitive to BC. There was little difference in the amount of carbenicillin, gentamicin sulfate, or rifampin needed to prevent growth of either the BCS or BC-resistant (BCR) strains. Growth of BCR cells was inhibited by ethylenediaminetetraacetate at a concentration of 400 μg/ml or less, whereas the BCS strain grew at ethylenediaminetetraacetate levels of 10,000 μg/ml. Phenylmercuric acetate and thimerosal inhibited growth of BCR and BCS cells at concentrations of 10 μg/ml or less. BCR cells were cross-resistant to >1,000 μg/ml concentrations of five other quaternary ammonium compounds, including three with C16 alkyls and two with alkyl groups of shorter length. The BCS strain was also resistant to >1,000 μg/ml concentrations of the three quaternary ammonium compounds with C16 alkyl groups but, in addition to BC, was inhibited by 200 μg/ml levels or less of the two quaternary ammonium compounds containing alkyl groups of less than 16 carbon atoms. PMID:4998348

  12. Review: Mechanisms of ammonium toxicity and the quest for tolerance.

    PubMed

    Esteban, Raquel; Ariz, Idoia; Cruz, Cristina; Moran, Jose Fernando

    2016-07-01

    Ammonium sensitivity of plants is a worldwide problem, constraining crop production. Prolonged application of ammonium as the sole nitrogen source may result in physiological and morphological disorders that lead to decreased plant growth and toxicity. The main causes of ammonium toxicity/tolerance described until now include high ammonium assimilation by plants and/or low sensitivity to external pH acidification. The various ammonium transport-related components, especially the non-electrogenic influx of NH3 (related to the depletion of (15)N) and the electrogenic influx of NH4(+), may contribute to ammonium accumulation, and therefore to NH3 toxicity. However, this accumulation may be influenced by increasing K(+) concentration in the root medium. Recently, new insights have been provided by "omics" studies, leading to a suggested involvement of GDP mannose-pyrophosphorylase in the response pathways of NH4(+) stress. In this review, we highlight the cross-talk signaling between nitrate, auxins and NO, and the importance of the connection of the plants' urea cycle to metabolism of polyamines. Overall, the tolerance and amelioration of ammonium toxicity are outlined to improve the yield of ammonium-grown plants. This review identifies future directions of research, focusing on the putative importance of aquaporins in ammonium influx, and on genes involved in ammonium sensitivity and tolerance. PMID:27181951

  13. The comparative effects of feeding ammonium carbonate, ammonium sulfate, and ammonium chloride on urinary calcium excretion in the rat.

    PubMed

    Whiting, S J; Cole, D E

    1987-11-01

    When either sulfate or chloride is added to the diet, the resulting acid load causes a rise in urinary calcium excretion. There is, however, the possibility that sulfate, which has been shown to complex renal tubular calcium, will further decrease renal calcium reabsorption and thus produce a greater calciuria than chloride. Because addition of a fixed cation (e.g., sodium) to the diet may also stimulate calciuresis, experiments were conducted using metabolizable ammonium to minimize cation effects. Ammonium salts of sulfate, chloride, and carbonate (control) were added to the diets of male rats at 0.3 mequiv./g weight of diet. Twenty-four hour excretion rates of calcium, sulfate, chloride, and net acid were measured at various intervals up to 1 month. As expected, the chloride and sulfate diets were both associated with significantly elevated urine calcium and net acid excretion as compared with controls. However, those fed sulfate exhibited significantly less calcium and acid excretion and absorbed a smaller proportion of the anion load than those given chloride. In a second experiment, the amounts of supplemental sulfate and chloride were adjusted so that total absorptions were similar. At 2 weeks, both calcium and acid excretions in the fixed anion groups were no longer significantly different. Thus, in chronic feeding trials, there appears to be no measurable difference in the calciuretic properties of sulfate and chloride anions. PMID:3449184

  14. A role for tungsten in the biology of Campylobacter jejuni: tungstate stimulates formate dehydrogenase activity and is transported via an ultra-high affinity ABC system distinct from the molybdate transporter.

    PubMed

    Smart, Jonathan P; Cliff, Matthew J; Kelly, David J

    2009-11-01

    The food-borne pathogen Campylobacter jejuni possesses no known tungstoenzymes, yet encodes two ABC transporters (Cj0300-0303 and Cj1538-1540) homologous to bacterial molybdate (ModABC) uptake systems and the tungstate transporter (TupABC) of Eubacterium acidaminophilum respectively. The actual substrates and physiological role of these transporters were investigated. Tryptophan fluorescence spectroscopy and isothermal titration calorimetry of the purified periplasmic binding proteins of each system revealed that while Cj0303 is unable to discriminate between molybdate and tungstate (K(D) values for both ligands of 4-8 nM), Cj1540 binds tungstate with a K(D) of 1.0 +/- 0.2 pM; 50 000-fold more tightly than molybdate. Induction-coupled plasma mass spectroscopy of single and double mutants showed that this large difference in affinity is reflected in a lower cellular tungsten content in a cj1540 (tupA) mutant compared with a cj0303c (modA) mutant. Surprisingly, formate dehydrogenase (FDH) activity was decreased approximately 50% in the tupA strain, and supplementation of the growth medium with tungstate significantly increased FDH activity in the wild type, while inhibiting known molybdoenzymes. Our data suggest that C. jejuni possesses a specific, ultra-high affinity tungstate transporter that supplies tungsten for incorporation into FDH. Furthermore, possession of two MoeA paralogues may explain the formation of both molybdopterin and tungstopterin in this bacterium. PMID:19818021

  15. Spectroscopy and structural characteristics of Eu3+-activated perovskite tungstate Ba2La2ZnW2O12

    NASA Astrophysics Data System (ADS)

    Yang, Li; Huang, Yanlin; Cheng, Han; Seo, Hyo Jin

    2015-11-01

    Eu3+-doped tungstate Ba2La2ZnW2O12 was prepared by the high-temperature solid-state reaction method. The x-ray powder diffraction (XRD) patterns indicate that the matrix has a perovskite structure. The samples were characterized by the scanning electron microscope (SEM), by optical diffuse reflection, photoluminescence (PL) spectra and by their decay curves. Eu3+-activated Ba2La2ZnW2O12 shows red luminescence under the excitation of near-ultraviolet and blue light. Laser site-selective excitation and emission spectroscopy technology was applied to investigate the spectroscopic and microstructural properties. The excitation spectra were tested by monitoring the emission from 5D0  →  7F0-4 transitions. Accordingly the emission spectra and decay curves (lifetime) were measured by the excitation in the 5D0  →  7F0 wavelength region using a pulsed, tunable, and narrow-band dye laser. We have detected two Eu3+ sites in Ba2La2ZnW2O12 with the temperature region ranging from 10 K to below 300 K. On the spectra data of the site-selective emission and decay, the Stark energy levels of Eu3+ at two different sites were determined. The lifetimes of Eu3+ ions at the two sites were compared. The energy transfer and crystallographic assignments for the Eu3+ sites were discussed.

  16. Lasing properties of selectively pumped Raman-active Nd{sup 3+}-doped molybdate and tungstate crystals

    SciTech Connect

    Basiev, Tasoltan T; Doroshenko, Maxim E; Ivleva, Lyudmila I; Osiko, Vyacheslav V; Kosmyna, M B; Komar', V K; Sulc, J; Jelinkova, H

    2006-08-31

    The lasing efficiency of Nd{sup 3+} ions is studied in laser materials capable of self-Raman frequency conversion. The lasing properties of tungstate and molybdate crystals with the scheelite structure (SrWO{sub 4}, BaWO{sub 4}, PbWO{sub 4}, SrMoO{sub 4}, PbMoO{sub 4}) activated with neodymium ions are investigated upon longitudinal pumping by a 750-nm alexandrite laser or a 800-nm diode laser. The slope lasing efficiency obtained for a Nd{sup 3+}:PbMoO{sub 4} laser emitting at 1054 nm is 54.3% for the total lasing efficiency of 46%, which is the best result for all the crystals with the scheelite structure studied so far. The simultaneous Q-switched lasing and self-Raman frequency conversion were demonstrated in neodymium-doped SrWO{sub 4}, PbWO{sub 4}, and BaWO{sub 4} crystals. (papers devoted to the 90th anniversary of a.m.prokhorov)

  17. [Achievement of Sulfate-Reducing Anaerobic Ammonium Oxidation Reactor Started with Nitrate-Reducting Anaerobic Ammonium Oxidation].

    PubMed

    Liu, Zheng-chuan; Yuan, Lin-jiang; Zhou, Guo-biao; Li, Jing

    2015-09-01

    The transformation of nitrite-reducing anaerobic ammonium oxidation to sulfate-reducing anaerobic ammonium oxidation in an UASB was performed and the changes in microbial community were studied. The result showed that the sulfate reducing anaerobic ammonium oxidation process was successfully accomplished after 177 days' operation. The removal rate of ammonium nitrogen and sulfate were up to 58. 9% and 15. 7%, the removing load of ammonium nitrogen and sulfate were 74. 3 mg.(L.d)-1 and 77. 5 mg.(L.d)-1 while concentration of ammonium nitrogen and sulfate of influent were 130 mg.(L.d)-1 and 500 mg.(L.d)-1, respectively. The lost nitrogen and sulphur was around 2 in molar ratio. The pH value of the effluent was lower than that of the influent. Instead of Candidatus brocadia in nitrite reducing anaerobic ammonium oxidation granular sludge, Bacillus benzoevorans became the dominant species in sulfate reducing anaerobic ammonium oxidation sludge. The dominant bacterium in the two kinds of anaerobic ammonium oxidation process is different. Our results imply that the two anaerobic ammonium oxidation processes are carried out by different kind of bacterium. PMID:26717697

  18. Ammonium release from a blanket peatland into headwater stream systems.

    PubMed

    Daniels, S M; Evans, M G; Agnew, C T; Allott, T E H

    2012-04-01

    Hydrochemical sampling of South Pennine (UK) headwater streams draining eroded upland peatlands demonstrates these systems are nitrogen saturated, with significant leaching of dissolved inorganic nitrogen (DIN), particularly ammonium, during both stormflow and baseflow conditions. DIN leaching at sub-catchment scale is controlled by geomorphological context; in catchments with low gully densities ammonium leaching dominates whereas highly gullied catchments leach ammonium and nitrate since lower water tables and increased aeration encourages nitrification. Stormflow flux calculations indicate that: approximately equivalent amounts of nitrate are deposited and exported; ammonium export significantly exceeds atmospheric inputs. This suggests two ammonium sources: high atmospheric loadings; and mineralisation of organic nitrogen stored in peat. Downstream trends indicate rapid transformation of leached ammonium into nitrate. It is important that low-order headwater streams are adequately considered when assessing impacts of atmospheric loads on the hydrochemistry of stream networks, especially with respect to erosion, climate change and reduced precipitation. PMID:22285801

  19. Mild ammonium stress increases chlorophyll content in Arabidopsis thaliana

    PubMed Central

    Sanchez-Zabala, Joseba; González-Murua, Carmen; Marino, Daniel

    2015-01-01

    Nitrate (NO3−) and ammonium (NH4+) are the main forms of nitrogen available in the soil for plants. Excessive NH4+ accumulation in tissues is toxic for plants and exclusive NH4+-based nutrition enhances this effect. Ammonium toxicity syndrome commonly includes growth impairment, ion imbalance and chlorosis among others. In this work, we observed high intraspecific variability in chlorophyll content in 47 Arabidopsis thaliana natural accessions grown under 1 mM NH4+ or 1 mM NO3− as N-source. Interestingly, chlorophyll content increased in every accession upon ammonium nutrition. Moreover, this increase was independent of ammonium tolerance capacity. Thus, chlorosis seems to be an exclusive effect of severe ammonium toxicity while mild ammonium stress induces chlorophyll accumulation. PMID:25853545

  20. Utilization of by-product ammonium sulfate

    SciTech Connect

    Boles, J.L.

    1992-12-31

    Sulfur is generally referred to as a secondary plant nutrients but it actually ranks in importance with nitrogen and phosphorous in protein synthesis. It is also an integral part of vitamins and enzymes essential to life. Soils in many areas of the world today are deficient in sulfur and soil sulfur reserves are being rapidly depleted. To address growing agronomic needs for sulfur, TVA`s National Fertilizer and Environmental Research Center (NFERC) has been committed to development of technologies to produce low-cost sulfur-containing fertilizers since the mid 1970`s. In the late 1970`s and early 1980`s, NFERC developed and demonstrated a 29-0-0-5S urea-ammonium sulfate (UAS) suspension. In 1984, NFERC developed and later patented a new family of nitrogen-sulfur (NS) suspensions to replace the earlier UAS suspension with more versatile, better quality products made by a simpler, more economical process. NFERC`s current endeavors involve development of technologies for successful utilization of low-quality, by-product ammonium sulfate (AS) in the fertilizer industry, which is the subject of this paper. NFERC`s current focus on utilization of by-product AS centers around the economic and environmental aspects of these technologies as the primary rationale for development, since the needs for sulfur in soils is now generally well known and sulfur application is common and now charged for in many areas.

  1. Utilization of by-product ammonium sulfate

    SciTech Connect

    Boles, J.L.

    1992-01-01

    Sulfur is generally referred to as a secondary plant nutrients but it actually ranks in importance with nitrogen and phosphorous in protein synthesis. It is also an integral part of vitamins and enzymes essential to life. Soils in many areas of the world today are deficient in sulfur and soil sulfur reserves are being rapidly depleted. To address growing agronomic needs for sulfur, TVA's National Fertilizer and Environmental Research Center (NFERC) has been committed to development of technologies to produce low-cost sulfur-containing fertilizers since the mid 1970's. In the late 1970's and early 1980's, NFERC developed and demonstrated a 29-0-0-5S urea-ammonium sulfate (UAS) suspension. In 1984, NFERC developed and later patented a new family of nitrogen-sulfur (NS) suspensions to replace the earlier UAS suspension with more versatile, better quality products made by a simpler, more economical process. NFERC's current endeavors involve development of technologies for successful utilization of low-quality, by-product ammonium sulfate (AS) in the fertilizer industry, which is the subject of this paper. NFERC's current focus on utilization of by-product AS centers around the economic and environmental aspects of these technologies as the primary rationale for development, since the needs for sulfur in soils is now generally well known and sulfur application is common and now charged for in many areas.

  2. Reassimilation of ammonium in Lotus japonicus.

    PubMed

    Betti, Marco; García-Calderón, Margarita; Pérez-Delgado, Carmen M; Credali, Alfredo; Pal'ove-Balang, Peter; Estivill, Guillermo; Repčák, Miroslav; Vega, José M; Galván, Francisco; Márquez, Antonio J

    2014-10-01

    This review summarizes the most recent results obtained in the analysis of two important metabolic pathways involved in the release of internal sources of ammonium in the model legume Lotus japonicus: photorespiratory metabolism and asparagine breakdown mediated by aparaginase (NSE). The use of photorespiratory mutants deficient in plastidic glutamine synthetase (GS2) enabled us to investigate the transcriptomics and metabolomic changes associated with photorespiratory ammonium accumulation in this plant. The results obtained indicate the existence of a coordinate regulation of genes involved in photorespiratory metabolism. Other types of evidence illustrate the multiple interconnections existing among the photorespiratory pathway and other processes such as intermediate metabolism, nodule function, and secondary metabolism in this plant, all of which are substantially affected in GS2-deficient mutants because of the impairment of the photorespiratory cycle. Finally, the importance of asparagine metabolism in L. japonicus is highlighted because of the fact that asparagine constitutes the vast majority of the reduced nitrogen translocated between different organs of this plant. The different types of NSE enzymes and genes which are present in L. japonicus are described. There is a particular focus on the most abundant K(+)-dependent LjNSE1 isoform and how TILLING mutants were used to demonstrate by reverse genetics the importance of this particular isoform in plant growth and seed production. PMID:24948681

  3. Safety Testing of Ammonium Nitrate Based Mixtures

    NASA Astrophysics Data System (ADS)

    Phillips, Jason; Lappo, Karmen; Phelan, James; Peterson, Nathan; Gilbert, Don

    2013-06-01

    Ammonium nitrate (AN)/ammonium nitrate based explosives have a lengthy documented history of use by adversaries in acts of terror. While historical research has been conducted on AN-based explosive mixtures, it has primarily focused on detonation performance while varying the oxygen balance between the oxidizer and fuel components. Similarly, historical safety data on these materials is often lacking in pertinent details such as specific fuel type, particle size parameters, oxidizer form, etc. A variety of AN-based fuel-oxidizer mixtures were tested for small-scale sensitivity in preparation for large-scale testing. Current efforts focus on maintaining a zero oxygen-balance (a stoichiometric ratio for active chemical participants) while varying factors such as charge geometry, oxidizer form, particle size, and inert diluent ratios. Small-scale safety testing was conducted on various mixtures and fuels. It was found that ESD sensitivity is significantly affected by particle size, while this is less so for impact and friction. Thermal testing is in progress to evaluate hazards that may be experienced during large-scale testing.

  4. Molecular mechanism of anaerobic ammonium oxidation.

    PubMed

    Kartal, Boran; Maalcke, Wouter J; de Almeida, Naomi M; Cirpus, Irina; Gloerich, Jolein; Geerts, Wim; Op den Camp, Huub J M; Harhangi, Harry R; Janssen-Megens, Eva M; Francoijs, Kees-Jan; Stunnenberg, Hendrik G; Keltjens, Jan T; Jetten, Mike S M; Strous, Marc

    2011-11-01

    Two distinct microbial processes, denitrification and anaerobic ammonium oxidation (anammox), are responsible for the release of fixed nitrogen as dinitrogen gas (N(2)) to the atmosphere. Denitrification has been studied for over 100 years and its intermediates and enzymes are well known. Even though anammox is a key biogeochemical process of equal importance, its molecular mechanism is unknown, but it was proposed to proceed through hydrazine (N(2)H(4)). Here we show that N(2)H(4) is produced from the anammox substrates ammonium and nitrite and that nitric oxide (NO) is the direct precursor of N(2)H(4). We resolved the genes and proteins central to anammox metabolism and purified the key enzymes that catalyse N(2)H(4) synthesis and its oxidation to N(2). These results present a new biochemical reaction forging an N-N bond and fill a lacuna in our understanding of the biochemical synthesis of the N(2) in the atmosphere. Furthermore, they reinforce the role of nitric oxide in the evolution of the nitrogen cycle. PMID:21964329

  5. Interaction of heavy metal ions with ammonium humates

    SciTech Connect

    Budaeva, A.D.; Zoltoev, E.V.; Tikhova, V.D.; Bodoev, N.V.

    2006-06-15

    Sorption properties of ammonium humates with respect to Fe(III), Cu(II), Al(III), Ni(II), Pb(II), and Zn(II) are studied. The effect of the metal ion concentration on the ammonium humate consumption is examined and the corresponding dependences are analyzed using regression equations. The IR spectra of brown coal humic acids, ammonium humates, as well as Fe, Cu, Ni, Zn, Pb, and Al humates are presented.

  6. Ammonium dichromate poisoning: A rare cause of acute kidney injury

    PubMed Central

    Radhakrishnan, H.; Gopi, M.; Arumugam, A.

    2014-01-01

    Ammonium dichromate is an inorganic compound frequently used in screen and color printing. Being a strong oxidizing agent, it causes oxygen free radical injury resulting in organ failure. We report a 25-year-old female who presented with acute kidney injury after consumption of ammonium dichromate. She was managed successfully with hemodialysis and supportive measures. This case is reported to highlight the toxicity of ammonium dichromate. PMID:25484533

  7. Evidence for ammonium-bearing minerals in Ceres

    NASA Technical Reports Server (NTRS)

    King, T. V. V.; Clark, R. N.; Calvin, W. M.; Sherman, D. M.; Swayze, G. A.; Brown, R. H.

    1991-01-01

    Evidence for ammonium-bearing minerals was found on the surface of the largest asteroid Ceres. The presence of ammonium-bearing clays suggests that Ceres has experienced a period of alteration by substantial amounts of an ammonium-bearing fluid. The presence of the ammonium-bearing clays does not preclude Ceres maintaining a volatile inventory in the core or in a volatile-rich zone at some distance below the surface. Telescopic observations of Ceres, using the 3.0 meter NASA Infrared telescope facility prompted this reevaluation of its surface mineralogy.

  8. Immunotoxic effects of sodium tungstate dihydrate on female B6C3F1/N mice when administered in drinking water.

    PubMed

    Frawley, Rachel P; Smith, Matthew J; White, Kimber L; Elmore, Susan A; Herbert, Ron; Moore, Rebecca; Staska, Lauren M; Behl, Mamta; Hooth, Michelle J; Kissling, Grace E; Germolec, Dori R

    2016-09-01

    Tungsten is a naturally occurring, high-tensile strength element that has been used in a number of consumer products. Tungsten has been detected in soil, waterways, groundwater, and human tissue and body fluids. Elevated levels of tungsten in urine were reported for populations exposed to tungstate in drinking water in areas where natural tungsten formations were prevalent. Published reports indicated that sodium tungstate may modulate hematopoiesis, immune cell populations, and immune responses in rodent models. The objective of this study was to assess potential immunotoxicity of sodium tungstate dihydrate (STD), a drinking water contaminant. Female B6C3F1/N mice received 0-2000 mg STD/L in their drinking water for 28 d, and were evaluated for effects on immune cell populations in spleen and bone marrow, and humoral-mediated, cell-mediated, and innate immunity. Three different parameters of cell-mediated immunity were similarly affected at 1000 mg STD/L. T-cell proliferative responses against allogeneic leukocytes and anti-CD3 were decreased 32%, and 21%, respectively. Cytotoxic T-lymphocyte activity was decreased at all effector:target cell ratios examined. At 2000 mg STD/L, the absolute numbers of CD3(+) T-cell progenitor cells in bone marrow were increased 86%, but the alterations in B-lymphocyte and other progenitor cells were not significant. There were no effects on bone marrow DNA synthesis or colony forming capabilities. STD-induced effects on humoral-mediated immunity, innate immunity, and splenocyte sub-populations were limited. Enhanced histopathology did not detect treatment-related lesions in any of the immune tissues. These data suggest exposure to STD in drinking water may adversely affect cell-mediated immunity. PMID:27223060

  9. [A case of ammonium urate urinary stone].

    PubMed

    Hara, Noboru; Koike, Hiroshi

    2004-05-01

    An 18-year-old female, who had undergone antireflux surgery for bilateral vesicoureteral reflux 5 years ago, was admitted to our department with complaints of fever and left-sided back pain. Bilateral renal stones and pyelonephritis were diagnosed after roentgenography, ultrasonography and urinalysis. Pyelonephritis was successfully treated with antibiotics and the left renal stone was completely disintegrated with extracorporeal shock wave lithotripsy. Spectrophotometric analysis revealed that the stone was composed of pure ammonium urate (AU). The patient had not experienced any episodes of urinary tract infection from the antireflux surgery until the present event, but had lost 20 kg in body weight during the last year due to a low-caloric diet and laxative abuse. AU urinary stones have been infrequently reported in Japan, and they are supposed to be associated with a low-caloric diet, laxative abuse, and anorexia nervosa. PMID:15237492

  10. Unsteady growth of ammonium chloride dendrites

    NASA Astrophysics Data System (ADS)

    Martyushev, L. M.; Terentiev, P. S.; Soboleva, A. S.

    2016-02-01

    Growth of ammonium chloride dendrites from aqueous solution is experimentally investigated. The growth rate υ and the radius ρ of curvature of branches are measured as a function of the relative supersaturation Δ for steady and unsteady growth conditions. It is shown that the experimental results are quantitatively described by the dependences ρ=a/Δ+b, υ=сΔ2, where the factors for primary branches are a=(1.3±0.2)·10-7 m, b=(2.5±0.4)·10-7 m, and c=(2.2±0.3)·10-4 m/s. The factor c is found to be approximately 7 times smaller for the side branches than that for the primary branches.

  11. Shock Compression of Ammonium Perchlorate Single Crystals

    NASA Astrophysics Data System (ADS)

    Gupta, Y. M.; Yuan, Gang; Feng, Ruqiang

    1997-07-01

    The shock response of ammonium perchlorate (AP) single crystals has been examined for uniaxial strain compression along the [210] and [001] directions. Quartz gauge and VISAR measurements have provided the wave profiles at the impact surface and after propagation through thin samples (1-3 mm thickness) for peak stresses ranging between 10 and 65 kbar. A two wave structure due to elastic-plastic deformation was observed for both orientations. The measured HEL values for the [210] and [001] orientations were about 4.3 and 3.5 kbar, respectively. Data for the two orientations reveal small stress relaxation effects and small differences due to crystal orientation effects. We have chosen to fit both sets of results with a simple elastic-perfectly plastic model used for isotropic materials. Reasonable agreement between the calculations and experimental results was obtained. Over the stress range examined to date, no evidence of chemical decomposition was observed for the time durations in our experiments.

  12. Allyl­ammonium hydrogen oxalate hemihydrate

    PubMed Central

    Dziuk, Błażej; Zarychta, Bartosz; Ejsmont, Krzysztof

    2014-01-01

    In the title hydrated mol­ecular salt, C3H8N+·C2HO4 −·0.5H2O, the water O atom lies on a crystallographic twofold axis. The C=C—C—N torsion angle in the cation is 2.8 (3)° and the dihedral angle between the CO2 and CO2H planes in the anion is 1.0 (4)°. In the crystal, the hydrogen oxalate ions are linked by O—H⋯O hydrogen bonds, generating [010] chains. The allyl­ammonium cations bond to the chains through N—H⋯O and N—H⋯(O,O) hydrogen bonds. The water mol­ecule accepts two N—H⋯O hydrogen bonds and makes two O—H⋯O hydrogen bonds. Together, the hydrogen bonds generate (100) sheets. PMID:25249903

  13. Kinetic approach to evaluate the energy and entropy of activation for the exchange of alkaline earth metal ions on tin(IV) tungstate cation exchanger

    SciTech Connect

    Varshney, K.G.; Khan, A.A.; Varshney, K.; Agrawal, S.

    1984-01-01

    A new approach based on the Nernst-Planck equations has been applied to study the reaction kinetics on the surface of tin(IV) tungstate for the Mg(II)-H(I), Ca(II)-H(I), Sr(II)-H(I) and Ba(II)-H(I) exchanges under the conditions favouring a particle diffusion phenomenon. On the basis of these studies the various physical parameters such as the effective diffusion coefficients, activation energies and entropies of activation have been evaluated which give some informations regarding the mechanism of ion-exchange on the surface of inorganic materials. 25 references, 3 figures, 3 tables.

  14. Decavanadate, decaniobate, tungstate and molybdate interactions with sarcoplasmic reticulum Ca(2+)-ATPase: quercetin prevents cysteine oxidation by vanadate but does not reverse ATPase inhibition.

    PubMed

    Fraqueza, Gil; Batista de Carvalho, Luís A E; Marques, M Paula M; Maia, Luisa; Ohlin, C André; Casey, William H; Aureliano, Manuel

    2012-11-01

    Recently we demonstrated that the decavanadate (V(10)) ion is a stronger Ca(2+)-ATPase inhibitor than other oxometalates, such as the isoelectronic and isostructural decaniobate ion, and the tungstate and molybdate monomer ions, and that it binds to this protein with a 1 : 1 stoichiometry. The V(10) interaction is not affected by any of the protein conformations that occur during the process of calcium translocation (i.e. E1, E1P, E2 and E2P) (Fraqueza et al., J. Inorg. Biochem., 2012). In the present study, we further explore this subject, and we can now show that the decaniobate ion, [Nb(10) = Nb(10)O(28)](6-), is a useful tool in deducing the interaction and the non-competitive Ca(2+)-ATPase inhibition by the decavanadate ion [V(10) = V(10)O(28)](6-). Moreover, decavanadate and vanadate induce protein cysteine oxidation whereas no effects were detected for the decaniobate, tungstate or molybdate ions. The presence of the antioxidant quercetin prevents cysteine oxidation, but not ATPase inhibition, by vanadate or decavanadate. Definitive V(IV) EPR spectra were observed for decavanadate in the presence of sarcoplasmic reticulum Ca(2+)-ATPase, indicating a vanadate reduction at some stage of the protein interaction. Raman spectroscopy clearly shows that the protein conformation changes that are induced by V(10), Nb(10) and vanadate are different from the ones induced by molybdate and tungstate monomer ions. Here, Mo and W cause changes similar to those by phosphate, yielding changes similar to the E1P protein conformation. The putative reduction of vanadium(V) to vanadium(IV) and the non-competitive binding of the V(10) and Nb(10) decametalates may explain the differences in the Raman spectra compared to those seen in the presence of molybdate or tungstate. Putting it all together, we suggest that the ability of V(10) to inhibit the Ca(2+)-ATPase may be at least in part due to the process of vanadate reduction and associated protein cysteine oxidation. These

  15. Development of radiopure cadmium tungstate crystal scintillators from enriched {sup 106}Cd and {sup 116}Cd to search for double beta decay

    SciTech Connect

    Danevich, F. A.; Boiko, R. S.; Chernyak, D. M.; Kobychev, V. V.; Kropivyansky, B. N.; Mokina, V. M.; Nikolaiko, A. S.; Poda, D. V.; Podviyanuk, R. B.; Tretyak, V. I.; Barabash, A. S.; Konovalov, S. I.; Umatov, V. I.; Belli, P.; Bernabei, R.; D'Angelo, S.; Brudanin, V. B.; Cappella, F.; Incicchitti, A.; Caracciolo, V.; and others

    2013-08-08

    Cadmium tungstate crystal scintillators enriched in {sup 106}Cd up to 66% ({sup 106}CdWO{sub 4}) and in {sup 116}Cd up to 82% ({sup 116}CdWO{sub 4}) have been developed. The low radioactive contamination of the crystals measured on the level of ≤ 1.5 mBq/kg ({sup 40}K), ≤ 0.005 - 0.012 mBq/kg ({sup 226}Ra), 0.04 - 0.07 mBq/kg ({sup 228}Th) allows to carry out high sensitivity experiments to search for double beta processes in {sup 106}Cd and {sup 116}Cd.

  16. A Roughness Study of Ytterbium-Doped Potassium Yttrium Tungstate (YB: KYW) Thin-Disk Femtosecond Ablated Dentin

    PubMed Central

    Liu, Jing; Chen, Hu; Ge, Wenqi; Wang, Yongbo; Sun, Yuchun; Wang, Yong; Lü, Peijun

    2014-01-01

    Introduction: The aim of this study was to evaluate the morphological changes and quantitatively assess the roughness of dentin after the ablation with a Ytterbium-Doped Potassium Yttrium Tungstate (YB: KYW) thin-disk femtosecond pulsed laser of different fluences, scanning speeds and scanning distances. Method: Twelve extracted human premolars were sectioned into crowns and roots along the cementum-enamel junction, and then the crowns were cut longitudinally into sheets about 1.5 mm thick with a cutting machine. The dentin samples were fixed on a stage at focus plane. The laser beam was irradiated onto the samples through a galvanometric scanning system, so rectangular movement could be achieved. After ablation, the samples were examined with a scanning electron microscope and laser three-dimensional profile measurement microscope for morphology and roughness study.With increasing laser fluence, dentin samples exhibited more melting and resolidification of dentin as well as debris-like structure and occluded parts of dentinal tubules. Results: When at the scanning speed of 2400mm/s and scanning distance of 24μm, the surface roughness of dentin ablated with femtosecond pulsed laser decreased significantly and varied between values of dentin surface roughness grinded with two kinds of diamond burs with different grits. When at the scanning speed of 1200mm/s and scanning distance of 12μm, the surface roughness decreased slightly, and the surface roughness of dentin ablated with femtosecond pulsed laser was almost equal to that grinded with a low grit diamond bur. Conclusion: This study showed that increased laser influence may lead to more collateral damage and lower dentin surface roughness, while scanning speed and scanning distance were also negatively correlated with surface roughness. Adequate parameters should be chosen to achieve therapeutic benefits, and different parameters can result in diverse ablation results. PMID:25606337

  17. The potential reproductive, neurobehavioral and systemic effects of soluble sodium tungstate exposure in Sprague-Dawley rats

    SciTech Connect

    McInturf, S.M.; Bekkedal, M.Y.V.; Wilfong, E.; Arfsten, D.; Chapman, G.; Gunasekar, P.G.

    2011-07-15

    The debate on tungsten (W) is fostered by its continuous usage in military munitions. Reports demonstrate W solubilizes in soil and can migrate into drinking water supplies and, therefore, is a potential health risk to humans. This study evaluated the reproductive, systemic and neurobehavioral effects of sodium tungstate (NaW) in rats following 70 days of daily pre-and postnatal exposure via oral gavage to 5, 62.5 and 125 mg/kg/day of NaW through mating, gestation and weaning (PND 0-20). Daily administration of NaW produced no overt evidence of toxicity and had no apparent effect on mating success or offspring physical development. Distress vocalizations were elevated in F{sub 1} offspring from the high dose group, whereas righting reflex showed unexpected sex differences where males demonstrated faster righting than females; however, the effects were not dose-dependent. Locomotor activity was affected in both low and high-dose groups of F{sub 1} females. Low-dose group showed increased distance traveled, more time in ambulatory movements and less time in stereotypic behavior than controls or high dose animals. The high-dose group had more time in stereotypical movements than controls, and less time resting than controls and the lowest exposure group. Maternal retrieval was not affected by NaW exposure. Tungsten analysis showed a systemic distribution of NaW in both parents and offspring, with preferential uptake within the immune organs, including the femur, spleen and thymus. Histopathological evidence suggested no severe chronic injury or loss of function in these organs. However, the heart showed histological lesions, histiocytic inflammation from minimal to mild with cardiomyocyte degeneration and necrosis in several P{sub 0} animals of 125 mg NaW dose group. The result of this study suggests that pre and postnatal exposure to NaW may produce subtle neurobehavioral effects in offspring related to motor activity and emotionality.

  18. Crystal structures of deuterated sodium molybdate dihydrate and sodium tungstate dihydrate from time-of-flight neutron powder diffraction.

    PubMed

    Fortes, A Dominic

    2015-07-01

    Time-of-flight neutron powder diffraction data have been measured from ∼90 mol% deuterated isotopologues of Na2MoO4·2H2O and Na2WO4·2H2O at 295 K to a resolution of sin (θ)/λ = 0.77 Å(-1). The use of neutrons has allowed refinement of structural parameters with a precision that varies by a factor of two from the heaviest to the lightest atoms; this contrasts with the X-ray based refinements where precision may be > 20× poorer for O atoms in the presence of atoms such as Mo and W. The accuracy and precision of inter-atomic distances and angles are in excellent agreement with recent X-ray single-crystal structure refinements whilst also completing our view of the hydrogen-bond geometry to the same degree of statistical certainty. The two structures are isotypic, space-group Pbca, with all atoms occupying general positions, being comprised of edge- and corner-sharing NaO5 and NaO6 polyhedra that form layers parallel with (010) inter-leaved with planes of XO4 (X = Mo, W) tetra-hedra that are linked by chains of water mol-ecules along [100] and [001]. The complete structure is identical with the previously described molybdate [Capitelli et al. (2006 ▸). Asian J. Chem. 18, 2856-2860] but shows that the purported three-centred inter-action involving one of the water mol-ecules in the tungstate [Farrugia (2007 ▸). Acta Cryst. E63, i142] is in fact an ordinary two-centred 'linear' hydrogen bond. PMID:26279871

  19. Crystal structures of deuterated sodium molybdate dihydrate and sodium tungstate dihydrate from time-of-flight neutron powder diffraction

    PubMed Central

    Fortes, A. Dominic

    2015-01-01

    Time-of-flight neutron powder diffraction data have been measured from ∼90 mol% deuterated isotopologues of Na2MoO4·2H2O and Na2WO4·2H2O at 295 K to a resolution of sin (θ)/λ = 0.77 Å−1. The use of neutrons has allowed refinement of structural parameters with a precision that varies by a factor of two from the heaviest to the lightest atoms; this contrasts with the X-ray based refinements where precision may be > 20× poorer for O atoms in the presence of atoms such as Mo and W. The accuracy and precision of inter­atomic distances and angles are in excellent agreement with recent X-ray single-crystal structure refinements whilst also completing our view of the hydrogen-bond geometry to the same degree of statistical certainty. The two structures are isotypic, space-group Pbca, with all atoms occupying general positions, being comprised of edge- and corner-sharing NaO5 and NaO6 polyhedra that form layers parallel with (010) inter­leaved with planes of XO4 (X = Mo, W) tetra­hedra that are linked by chains of water mol­ecules along [100] and [001]. The complete structure is identical with the previously described molybdate [Capitelli et al. (2006 ▸). Asian J. Chem. 18, 2856–2860] but shows that the purported three-centred inter­action involving one of the water mol­ecules in the tungstate [Farrugia (2007 ▸). Acta Cryst. E63, i142] is in fact an ordinary two-centred ‘linear’ hydrogen bond. PMID:26279871

  20. Hydrothermal oxidation of organic wastes using reclaimed ammonium nitrate

    SciTech Connect

    Proesmans, P.I.; Luan, L.; Buelow, S.J.

    1996-04-01

    Ammonium nitrate is being studied as an alternative for ammonium perchlorate as an oxidizing agent in Department of Defense 1.1 and 1.3 rocket propellants. Use of ammonium nitrate would eliminate the HCl produced by ammonium perchlorate upon thermal decomposition. To stabilize the ammonium nitrate, which suffers from phase instability, potassium dinitramide (KDN) is added. This increased use of ammonium nitrate will ultimately create a need for environmentally responsible processes to reuse ammonium nitrate extracted from demilitarized rocket motors. Ammonium Nitrate was investigated as an oxidizing agent for methanol, acetic acid and phenol. High removal of organic, ammonia and nitrate was achieved at stoichiometric concentrations. The oxidation of ammonia by nitrate was much faster than the oxidation of either methanol or acetic acid. Phenol, however, was in strong competition with ammonia for the oxidizer (nitrate). Nitrogen products included N{sub 2}, N{sub 2}O, NO{sub 2{sup {minus}}} as well as toxic NO and trace amounts of NO{sub 2}. Carbon products were CO{sub 2}, HCO{sub 3{sup {minus}}}, CO{sub 3}{sup 2{minus}}, and CO.

  1. THE MASS ACCOMMODATION COEFFICIENT OF AMMONIUM NITRATE AEROSOL. (R823514)

    EPA Science Inventory

    The mass transfer rate of pure ammonium nitrate between the aerosol and gas phases was
    quantified experimentally by the use of the tandem differential mobility analyzer/scanning mobility
    particle sizer (TDMA/SMPS) technique. Ammonium nitrate particles 80-220 nm in diameter<...

  2. 40 CFR 721.655 - Ethoxylated alkyl quaternary ammonium compound.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... compound. 721.655 Section 721.655 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.655 Ethoxylated alkyl quaternary ammonium compound. (a) Chemical... as an ethoxylated alkyl quaternary ammonium compound (PMN P-96-573) is subject to reporting...

  3. 40 CFR 721.655 - Ethoxylated alkyl quaternary ammonium compound.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... compound. 721.655 Section 721.655 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.655 Ethoxylated alkyl quaternary ammonium compound. (a) Chemical... as an ethoxylated alkyl quaternary ammonium compound (PMN P-96-573) is subject to reporting...

  4. 40 CFR 721.655 - Ethoxylated alkyl quaternary ammonium compound.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... compound. 721.655 Section 721.655 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.655 Ethoxylated alkyl quaternary ammonium compound. (a) Chemical... as an ethoxylated alkyl quaternary ammonium compound (PMN P-96-573) is subject to reporting...

  5. 40 CFR 721.655 - Ethoxylated alkyl quaternary ammonium compound.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... compound. 721.655 Section 721.655 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.655 Ethoxylated alkyl quaternary ammonium compound. (a) Chemical... as an ethoxylated alkyl quaternary ammonium compound (PMN P-96-573) is subject to reporting...

  6. 40 CFR 721.655 - Ethoxylated alkyl quaternary ammonium compound.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... compound. 721.655 Section 721.655 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.655 Ethoxylated alkyl quaternary ammonium compound. (a) Chemical... as an ethoxylated alkyl quaternary ammonium compound (PMN P-96-573) is subject to reporting...

  7. 40 CFR 180.473 - Glufosinate ammonium; tolerances for residues.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 25 2012-07-01 2012-07-01 false Glufosinate ammonium; tolerances for residues. 180.473 Section 180.473 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) PESTICIDE PROGRAMS TOLERANCES AND EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES IN FOOD Specific Tolerances § 180.473 Glufosinate ammonium;...

  8. 21 CFR 73.1025 - Ferric ammonium citrate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Drugs § 73.1025 Ferric ammonium citrate. (a) Identity. The... green forms, are deliquescent in air, and are reducible by light. (b) Specifications. Ferric ammonium... from certification. Certification of this color additive is not necessary for the protection of...

  9. 21 CFR 73.1025 - Ferric ammonium citrate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Drugs § 73.1025 Ferric ammonium citrate. (a) Identity. The... green forms, are deliquescent in air, and are reducible by light. (b) Specifications. Ferric ammonium... from certification. Certification of this color additive is not necessary for the protection of...

  10. 21 CFR 73.1025 - Ferric ammonium citrate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Drugs § 73.1025 Ferric ammonium citrate. (a) Identity. The... green forms, are deliquescent in air, and are reducible by light. (b) Specifications. Ferric ammonium... from certification. Certification of this color additive is not necessary for the protection of...

  11. Racer (Ammonium Nonanoate) weed control evaluation for onions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Racer has been labeled as a herbicide for food use and is currently under consideration as an organic herbicide for organically grown food crops. The main component (40%) of Racer is ammonium nonanoate (ammonium pelargonate), which occurs in nature and primarily formed from biodegradation of higher...

  12. 46 CFR 148.220 - Ammonium nitrate-phosphate fertilizers.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 46 Shipping 5 2011-10-01 2011-10-01 false Ammonium nitrate-phosphate fertilizers. 148.220 Section... § 148.220 Ammonium nitrate-phosphate fertilizers. (a) This section applies to the stowage and transportation of uniform, nonsegregating mixtures of nitrogen/phosphate or nitrogen/potash type fertilizers,...

  13. 46 CFR 148.220 - Ammonium nitrate-phosphate fertilizers.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 46 Shipping 5 2013-10-01 2013-10-01 false Ammonium nitrate-phosphate fertilizers. 148.220 Section... § 148.220 Ammonium nitrate-phosphate fertilizers. (a) This section applies to the stowage and transportation of uniform, nonsegregating mixtures of nitrogen/phosphate or nitrogen/potash type fertilizers,...

  14. 46 CFR 148.220 - Ammonium nitrate-phosphate fertilizers.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 46 Shipping 5 2014-10-01 2014-10-01 false Ammonium nitrate-phosphate fertilizers. 148.220 Section... § 148.220 Ammonium nitrate-phosphate fertilizers. (a) This section applies to the stowage and transportation of uniform, nonsegregating mixtures of nitrogen/phosphate or nitrogen/potash type fertilizers,...

  15. 46 CFR 148.220 - Ammonium nitrate-phosphate fertilizers.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 46 Shipping 5 2012-10-01 2012-10-01 false Ammonium nitrate-phosphate fertilizers. 148.220 Section... § 148.220 Ammonium nitrate-phosphate fertilizers. (a) This section applies to the stowage and transportation of uniform, nonsegregating mixtures of nitrogen/phosphate or nitrogen/potash type fertilizers,...

  16. 40 CFR 721.6070 - Alkyl phosphonate ammonium salts.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Alkyl phosphonate ammonium salts. 721... Substances § 721.6070 Alkyl phosphonate ammonium salts. (a) Chemical substances and significant new uses... salts (PMNs P-93-725 and P-93-726) are subject to reporting under this section for the significant...

  17. 40 CFR 721.6070 - Alkyl phosphonate ammonium salts.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Alkyl phosphonate ammonium salts. 721... Substances § 721.6070 Alkyl phosphonate ammonium salts. (a) Chemical substances and significant new uses... salts (PMNs P-93-725 and P-93-726) are subject to reporting under this section for the significant...

  18. 40 CFR 721.6070 - Alkyl phosphonate ammonium salts.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Alkyl phosphonate ammonium salts. 721... Substances § 721.6070 Alkyl phosphonate ammonium salts. (a) Chemical substances and significant new uses... salts (PMNs P-93-725 and P-93-726) are subject to reporting under this section for the significant...

  19. 40 CFR 721.6070 - Alkyl phosphonate ammonium salts.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Alkyl phosphonate ammonium salts. 721... Substances § 721.6070 Alkyl phosphonate ammonium salts. (a) Chemical substances and significant new uses... salts (PMNs P-93-725 and P-93-726) are subject to reporting under this section for the significant...

  20. 40 CFR 721.6070 - Alkyl phosphonate ammonium salts.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alkyl phosphonate ammonium salts. 721... Substances § 721.6070 Alkyl phosphonate ammonium salts. (a) Chemical substances and significant new uses... salts (PMNs P-93-725 and P-93-726) are subject to reporting under this section for the significant...

  1. IUPAC - NIST Solubility Data Series 66. Ammonium Phosphates

    NASA Astrophysics Data System (ADS)

    Eysseltová, Jitka; Dirkse, Thedford P.

    1998-11-01

    The solubility of ammonium phosphate is reviewed. Many ammonium phosphates can be described in terms of the ternary system: NH3-PO5-H2O. However, this system differs from systems like the sulfates and halates in that it has a marked tendency to form condensed oligophosphate ions. The literature survey covers the period up to 1988.

  2. Shock wave synthesis of amino acids from solutions of ammonium formate and ammonium bicarbonate

    NASA Astrophysics Data System (ADS)

    Suzuki, Chizuka; Furukawa, Yoshihiro; Kobayashi, Takamichi; Sekine, Toshimori; Nakazawa, Hiromoto; Kakegawa, Takeshi

    2015-07-01

    The emergence of life's building blocks, such as amino acids and nucleobases, on the prebiotic Earth was a critical step for the beginning of life. Reduced species with low mass, such as ammonia, amines, or carboxylic acids, are potential precursors for these building blocks of life. These precursors may have been provided to the prebiotic ocean by carbonaceous chondrites and chemical reactions related to meteorite impacts on the early Earth. The impact of extraterrestrial objects on Earth occurred more frequently during this period than at present. Such impacts generated shock waves in the ocean, which have the potential to progress chemical reactions to form the building blocks of life from reduced species. To simulate shock-induced reactions in the prebiotic ocean, we conducted shock-recovery experiments on ammonium bicarbonate solution and ammonium formate solution at impact velocities ranging from 0.51 to 0.92 km/s. In the products from the ammonium formate solution, several amino acids (glycine, alanine, ß-alanine, and sarcosine) and aliphatic amines (methylamine, ethylamine, propylamine, and butylamine) were detected, although yields were less than 0.1 mol % of the formic acid reactant. From the ammonium bicarbonate solution, smaller amounts of glycine, methylamine, ethylamine, and propylamine were formed. The impact velocities used in this study represent minimum cases because natural meteorite impacts typically have higher velocities and longer durations. Our results therefore suggest that shock waves could have been involved in forming life's building blocks in the ocean of prebiotic Earth, and potentially in aquifers of other planets, satellites, and asteroids.

  3. Hybrid organic-inorganic crystals based on ammonium dihydrogen phosphate and ammonium salicylate

    NASA Astrophysics Data System (ADS)

    Voronov, A. P.; Salo, V. I.; Puzikov, V. M.; Babenko, G. N.; Roshal, A. D.; Tkachenko, V. F.

    2011-11-01

    ADP-NH 4Sal hybrid crystals are grown from aqueous solutions. The influence of the acidity of the mixed solution on the conditions of co-crystallization of the components is studied. The spectral and scintillation characteristics are determined. Co-crystallization of ammonium salicylate (NH 4Sal) and ammonium dihydrogen phosphate (ADP, NH 4H 2PO 4) is shown to be feasible, the structure of the doping addition being defined by the solution рН. In basic and weak acidic media the hybrid crystals ADP:NH 4Sal are formed in which salicylate anions are located in the interplanar space between the {110}-type planes in the lattice of ADP. The luminescence spectra contain an emission band maximum with λ max=360 nm. In acidic solutions there are ADP:HSal crystals in which salicylic acid molecules captured by the growth macrosteps are located in the interplanar space of the prismatic {100} and pyramidal {101} growth sectors. The luminescence band undergoes bathochromic shift to λmax=400 nm. The sensitivity of ADP:NH 4Sal scintillation crystals to fast neutrons depends on the concentration of ammonium salicylate in ADP matrix. The highest neutron sensitivity is characteristic of the co-doped ADP:NH 4Sal/Tl scintillation crystals.

  4. Assimilation of ammonium and nitrate nitrogen by bean plants

    SciTech Connect

    Volk, R.J. ); Chaillou, S.; Morot-Gaudry, J.F. ); Mariotti, A. )

    1989-04-01

    Enhanced growth is often observed in plants growing on combined ammonium and nitrate nutrition. The physiological basis for such enhancement was examined by exposing non-nodulated bean (Phaseolus vulgaris L.) plants to {sup 15}N-labeled, 1.0 mM N solutions containing 0, 33, 67 or 100% of the N as ammonium, the balance being nitrate. Maximal total N uptake and biomass production were attained by plants receiving 33% ammonium. A higher proportion of incoming ammonium than nitrate was incorporated into root protein. This was accompanied by increased partitioning of plant biomass to roots. It was concluded that as a consequence of greater N metabolism in the root under mixed ammonium and nitrate nutrition, the root became a more active sink for photosynthate. Concurrently, the augmented supply of N to the shoot enhanced net photosynthesis as reflected in increased plant biomass.

  5. Ammonium Metabolism Enzymes Aid Helicobacter pylori Acid Resistance

    PubMed Central

    Miller, Erica F.

    2014-01-01

    The gastric pathogen Helicobacter pylori possesses a highly active urease to support acid tolerance. Urea hydrolysis occurs inside the cytoplasm, resulting in the production of NH3 that is immediately protonated to form NH4+. This ammonium must be metabolized or effluxed because its presence within the cell is counterproductive to the goal of raising pH while maintaining a viable proton motive force (PMF). Two compatible hypotheses for mitigating intracellular ammonium toxicity include (i) the exit of protonated ammonium outward via the UreI permease, which was shown to facilitate diffusion of both urea and ammonium, and/or (ii) the assimilation of this ammonium, which is supported by evidence that H. pylori assimilates urea nitrogen into its amino acid pools. We investigated the second hypothesis by constructing strains with altered expression of the ammonium-assimilating enzymes glutamine synthetase (GS) and glutamate dehydrogenase (GDH) and the ammonium-evolving periplasmic enzymes glutaminase (Ggt) and asparaginase (AsnB). H. pylori strains expressing elevated levels of either GS or GDH are more acid tolerant than the wild type, exhibit enhanced ammonium production, and are able to alkalize the medium faster than the wild type. Strains lacking the genes for either Ggt or AsnB are acid sensitive, have 8-fold-lower urea-dependent ammonium production, and are more acid sensitive than the parent. Additionally, we found that purified H. pylori GS produces glutamine in the presence of Mg2+ at a rate similar to that of unadenylated Escherichia coli GS. These data reveal that all four enzymes contribute to whole-cell acid resistance in H. pylori and are likely important for assimilation and/or efflux of urea-derived ammonium. PMID:24936052

  6. PULMONARY FUNCTION IN ELASTASE-TREATED GUINEA PIGS AND RATS EXPOSED TO AMMONIUM SULFATE OR AMMONIUM NITRATE AEROSOLS

    EPA Science Inventory

    Three weeks following intratracheal instillations of elastase dissolved in saline, or saline alone, guinea pigs and rats were exposed for 5 or 20 days, 6 hr/day, 5 days/week to filtered room air, 1 mg/cu.m. ammonium sulfate ((NH4)2SO4) or 1 mg/cu.m. ammonium nitrate (NH4NO3) aero...

  7. Ammonium and methylammonium transport in Rhodobacter sphaeroides

    SciTech Connect

    Cordts, M.L.; Gibson, J.

    1987-04-01

    Rhodobacter spheroides maintained intracellular ammonium pools of 1.1 to 2.6 mM during growth in several fixed nitrogen sources as well as during diazotrophic growth. Addition of 0.15 mM NH/sub 4//sup +/ to washed, nitrogen-free cell suspensions was followed by linear uptake of NH/sub 4//sup +/ from the medium and transient formation of intracellular pools of 0.9 to 1.5 mM NH/sub 4//sup +/. Transport of NH/sub 4//sup +/ was shown to be independent of assimilation by glutamine synthetase because intracellular pools of over 1 mM represented NH/sub 4//sup +/ concentration gradients of at least 100-fold across the cytoplasmic membrane. Ammonium pools of over 1 mM were also found in non-growing cell suspensions in nitrogen-free medium after glutamine synthetase was inhibited with methionine sulfoximine. In NH/sub 4//sup +/-free cell suspensions, methylammonium (/sup 14/CH/sub 3/NH/sub 3//sup +/) was taken up rapidly, and intracellular concentrations of 0.4 to 0.5 mM were maintained. The /sup 14/CN/sub 3/NH/sub 3//sup +/ pool was not affected by methionine sulfoximine. Unlike NH/sub 4//sup +/ uptake, /sup 14/CH/sub 3/NH/sub 3//sup +/ uptake in nitrogen-free cell suspensions was repressed by growth in NH/sub 4//sup +/. These results suggest that R. sphaeroides may produce an NH/sub 4//sup +/-specific transport system in addition to the NH/sub 4//sup +///sup 14/CH/sub 3/NH/sub 3//sup +/ transporter. This second transporter is able to produce normal-size NH/sub 4//sup +/ pools but has very little affinity for /sup 14/CH/sub 3/NH/sub 3//sup +/ and is not repressed by growth in high concentrations of NH/sub 4//sup +/.

  8. Population of Nitrifying Bacteria and Nitrification in Ammonium Saturated Clinoptilolite

    NASA Technical Reports Server (NTRS)

    McGilloway, R. L.; Weaver, R. W.; Ming, Douglas W.; Gruener, J.

    1999-01-01

    As humans begin to spend longer periods of time in space, plants will be incorporated into life support systems. Ammonium saturated clinoptilolite is one plant growth substrate but a balance between ammonium and nitrate is needed. A laboratory study was conducted to determine effects of nitrifying bacteria on ammonium concentrations and kinetics of nitrification. Columns containing clinoptilolite substrate amended with nitrifying bacteria obtained from soil enrichment were analyzed weekly for a 90 day period. The enrichment culture initially contained 1 x 10(exp 5) ammonium oxidizing bacteria and 1 x 10(exp 2) nitrite oxidizing bacteria per gram of substrate. Populations of ammonium oxidizing bacteria increased to 1 x 10(exp 6) and nitrite oxidizing bacteria increased to 1 x 10(exp 3) per gram of substrate. The nitrification rate was approximately 0.25mg NO3(-)-N/kg.hr. Experiments were also conducted to enumerate nitrifying bacteria in a clinoptilolite substrate used to grow wheat (Triticum aestivum L.). Seventy days following the initial inoculation with an unknown number of commercial nitrifying bacteria, 1 x 10(exp 5) ammonium oxidizing bacteria per gram of substrate were present. The number of nitrite oxidizing bacteria was between 1 x 10(exp 3) to 10(exp 4) per gram of substrate as measured by the most probable number method. Nitrification rates were approximately 0.20mg NO3(-)-N/kg.hr. Clinoptilolite readily exchanged sufficient concentrations of ammonium to support nitrifying bacteria and they survived well in this medium.

  9. Acclimation and toxicity of high ammonium concentrations to unicellular algae.

    PubMed

    Collos, Yves; Harrison, Paul J

    2014-03-15

    A literature review on the effects of high ammonium concentrations on the growth of 6 classes of microalgae suggests the following rankings. Mean optimal ammonium concentrations were 7600, 2500, 1400, 340, 260, 100 μM for Chlorophyceae, Cyanophyceae, Prymnesiophyceae, Diatomophyceae, Raphidophyceae, and Dinophyceae respectively and their tolerance to high toxic ammonium levels was 39,000, 13,000, 2300, 3600, 2500, 1200 μM respectively. Field ammonium concentrations <100 μM would not likely reduce the growth rate of most microalgae. Chlorophytes were significantly more tolerant to high ammonium than diatoms, prymnesiophytes, dinoflagellates, and raphidophytes. Cyanophytes were significantly more tolerant than dinoflagellates which were the least tolerant. A smaller but more complete data set was used to estimate ammonium EC₅₀ values, and the ranking was: Chlorophyceae>Cyanophyceae, Dinophyceae, Diatomophyceae, and Raphidophyceae. Ammonia toxicity is mainly attributed to NH₃ at pHs >9 and at pHs <8, toxicity is likely associated with the ammonium ion rather than ammonia. PMID:24533997

  10. Ammonium Hydrosulfide and Jupiter's Great Red Spot

    NASA Astrophysics Data System (ADS)

    Loeffler, M. J.; Hudson, R.; Chanover, N.; Simon, A. A.

    2014-12-01

    The color and composition of Jupiter's Great Red Spot (GRS) has been debated for more than a century. While there are numerous hypotheses for the origin of Jupiter's GRS, recent work suggests that the GRS's color could originate from multiple components (Carlson et al., 2012; Simon et al., submitted). In light of this, we have recently begun conducting in situ laboratory experiments that test whether ammonium hydrosulfide, NH4SH, or its radiation decomposition products contribute to the GRS spectrum. In this presentation, we will discuss some of our most recent results, where we have studied the stability of NH4SH samples as a function of temperature using infrared and mass spectrometry. Funding for this work has been provided by NASA's Planetary Atmospheres and Outer Planets Research programs. ReferencesCarlson, R. W., K. H. Baines, M. S. Anderson, G. Filacchione. Chromophores from photolyzed ammonia reacting with acetylene: Application to Jupiter's Great Red Spot, DPS, 44, 2012. Simon, A. A., J. Legarreta, F. Sanz-Requena, S. Perez-Hoyos, E. Garcia-Melendo, R. W. Carlson. Spectral Comparison and Stability of Red Regions on Jupiter. J. Geophys. Res. - Planets, submitted.

  11. Quaternary ammonium biocides: efficacy in application.

    PubMed

    Gerba, Charles P

    2015-01-01

    Quaternary ammonium compounds (QACs) are among the most commonly used disinfectants. There has been concern that their widespread use will lead to the development of resistant organisms, and it has been suggested that limits should be place on their use. While increases in tolerance to QACs have been observed, there is no clear evidence to support the development of resistance to QACs. Since efflux pumps are believe to account for at least some of the increased tolerance found in bacteria, there has been concern that this will enhance the resistance of bacteria to certain antibiotics. QACs are membrane-active agents interacting with the cytoplasmic membrane of bacteria and lipids of viruses. The wide variety of chemical structures possible has seen an evolution in their effectiveness and expansion of applications over the last century, including non-lipid-containing viruses (i.e., noroviruses). Selection of formulations and methods of application have been shown to affect the efficacy of QACs. While numerous laboratory studies on the efficacy of QACs are available, relatively few studies have been conducted to assess their efficacy in practice. Better standardized tests for assessing and defining the differences between increases in tolerance versus resistance are needed. The ecological dynamics of microbial communities where QACs are a main line of defense against exposure to pathogens need to be better understood in terms of sublethal doses and antibiotic resistance. PMID:25362069

  12. Quaternary Ammonium Biocides: Efficacy in Application

    PubMed Central

    2014-01-01

    Quaternary ammonium compounds (QACs) are among the most commonly used disinfectants. There has been concern that their widespread use will lead to the development of resistant organisms, and it has been suggested that limits should be place on their use. While increases in tolerance to QACs have been observed, there is no clear evidence to support the development of resistance to QACs. Since efflux pumps are believe to account for at least some of the increased tolerance found in bacteria, there has been concern that this will enhance the resistance of bacteria to certain antibiotics. QACs are membrane-active agents interacting with the cytoplasmic membrane of bacteria and lipids of viruses. The wide variety of chemical structures possible has seen an evolution in their effectiveness and expansion of applications over the last century, including non-lipid-containing viruses (i.e., noroviruses). Selection of formulations and methods of application have been shown to affect the efficacy of QACs. While numerous laboratory studies on the efficacy of QACs are available, relatively few studies have been conducted to assess their efficacy in practice. Better standardized tests for assessing and defining the differences between increases in tolerance versus resistance are needed. The ecological dynamics of microbial communities where QACs are a main line of defense against exposure to pathogens need to be better understood in terms of sublethal doses and antibiotic resistance. PMID:25362069

  13. [A case of ammonium urate urinary stones with anorexia nervosa].

    PubMed

    Komori, K; Arai, H; Gotoh, T; Imazu, T; Honda, M; Fujioka, H

    2000-09-01

    A 27-year-old woman had been suffering from bulimia and habitual vomiting for about 7 years and was incidentally found to have right renal stones by computed tomography. She was referred to our hospital for the treatment of these caluculi. On admission, she presented with hypokalemia, hypochloremia and metabolic alkalosis and was diagnosed with anorexia nervosa. Following successful removal by percutaneous nephrolithotripsy and extracorporeal shockwave lithotripsy the stones were found to consist of pure ammonium urate. Since the urine of an anorexia nervosa patient tends to be rich in uric acid and ammonium, anorexia nervosa seems to be associated with ammonium urate urinary stones. PMID:11107533

  14. Antimicrobial Polymeric Materials with Quaternary Ammonium and Phosphonium Salts

    PubMed Central

    Xue, Yan; Xiao, Huining; Zhang, Yi

    2015-01-01

    Polymeric materials containing quaternary ammonium and/or phosphonium salts have been extensively studied and applied to a variety of antimicrobial-relevant areas. With various architectures, polymeric quaternary ammonium/phosphonium salts were prepared using different approaches, exhibiting different antimicrobial activities and potential applications. This review focuses on the state of the art of antimicrobial polymers with quaternary ammonium/phosphonium salts. In particular, it discusses the structure and synthesis method, mechanisms of antimicrobial action, and the comparison of antimicrobial performance between these two kinds of polymers. PMID:25667977

  15. Rhizobium sp. strain ORS571 ammonium assimilation and nitrogen fixation.

    PubMed Central

    Donald, R G; Ludwig, R A

    1984-01-01

    Among rhizobia studied, Rhizobium sp. strain ORS571 alone grew unambiguously on N2 as sole N source. In ORS571 , only the glutamine synthetase (GS)-glutamate synthase ( GOGAT ) pathway assimilated ammonium. However, ORS571 exhibited two unique physiological aspects of this pathway: ORS571 had only GS I, whereas all other Rhizobiaceae studied had both GS I and GS II, and both NADPH- and NADH-dependent GOGAT activities were present. ORS571 GS-affected and NADPH- GOGAT -affected mutant strains were defective in both ammonium assimilation (Asm-) and N2 fixation (Nif-) in culture and in planta ; NADH- GOGAT mutants were Asm- but Nif+. "Bacteroid" GS activity was essentially nil, suggesting symbiotic ammonium export. Physiological studies on effects of glutamine, ammonium, methionine sulfoximine, and diazo-oxo-norleucine on nitrogenase induction in culture implied a regulatory role for the intracellular glutamine pool. Images PMID:6144666

  16. 21 CFR 73.2298 - Ferric ammonium ferrocyanide.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2298 Ferric ammonium ferrocyanide. (a... ferrocyanide is safe for use in coloring externally applied cosmetics, including cosmetics applied to the...

  17. 21 CFR 73.2298 - Ferric ammonium ferrocyanide.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2298 Ferric ammonium ferrocyanide. (a... ferrocyanide is safe for use in coloring externally applied cosmetics, including cosmetics applied to the...

  18. 21 CFR 73.2298 - Ferric ammonium ferrocyanide.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2298 Ferric ammonium ferrocyanide. (a... ferrocyanide is safe for use in coloring externally applied cosmetics, including cosmetics applied to the...

  19. 21 CFR 73.2298 - Ferric ammonium ferrocyanide.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2298 Ferric ammonium ferrocyanide. (a... ferrocyanide is safe for use in coloring externally applied cosmetics, including cosmetics applied to the...

  20. 21 CFR 73.2298 - Ferric ammonium ferrocyanide.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2298 Ferric ammonium ferrocyanide. (a... ferrocyanide is safe for use in coloring externally applied cosmetics, including cosmetics applied to the...

  1. Synthesis and Antibacterial Activity of Novel Quaternary Ammonium Pyridoxine Derivatives.

    PubMed

    Shtyrlin, Nikita V; Sapozhnikov, Sergey V; Koshkin, Sergey A; Iksanova, Alfiya G; Sabirov, Arthur H; Kayumov, Airat R; Nureeva, Aliya A; Zeldi, Marina I; Shtyrlin, Yurii G

    2015-01-01

    A series of 26 quaternary ammonium pyridoxine derivatives were synthesized and their cytotoxicity and antibacterial activities against clinically relevant bacterial strains were tested in vitro. The antibacterial activity of mono-ammonium salts increased with the rise of the lipophilicity and compound 3,3,5-trimethyl-8,8-dioctyl-1,7,8,9-tetrahydro-[1,3]dioxino[5,4-d]pyrrolo[3,4-b]pyridin-8-ium chloride (2d) reaches a maximum among them. Bis-ammonium salt of pyridoxine 4 with two dimethyloctylamine groups also demonstrated high antibacterial activity despite lower lipophilicity. The results of MTT assay indicated that HEK 293 cells were more sensitive than HSF to quaternary ammonium pyridoxine derivatives. Compounds 2d and 4 did not induce the damage of the DNA and might be of interest in the development of new antimicrobials. PMID:25938426

  2. Formation of urea and guanidine by irradiation of ammonium cyanide.

    NASA Technical Reports Server (NTRS)

    Lohrmann, R.

    1972-01-01

    Aqueous solutions of ammonium cyanide yield urea, cyanamide and guanidine when exposed to sunlight or an unfiltered 254 nm ultraviolet source. The prebiotic significance of these results is discussed.

  3. Direct esterification of ammonium salts of carboxylic acids

    DOEpatents

    Halpern, Yuval

    2003-06-24

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

  4. Methods to Stabilize and Destabilize Ammonium Borohydride

    SciTech Connect

    Nielsen, Thomas K.; Karkamkar, Abhijeet J.; Bowden, Mark E.; Besenbacher, Fleming; Jensen, Torben R.; Autrey, Thomas

    2013-01-21

    Ammonium borohydride, NH4BH4, has a high hydrogen content of ρm = 24.5 wt% H2 and releases 18 wt% H2 below T = 160 °C. However, the half-life of bulk NH4BH4 at ambient temperatures, ~6 h, is insufficient for practical applications. The decomposition of NH4BH4 (ABH2) was studied at variable hydrogen and argon back pressures to investigate possible pressure mediated stabilization effects. The hydrogen release rate from solid ABH2 at ambient temperatures is reduced by ~16 % upon increasing the hydrogen back pressure from 5 to 54 bar. Similar results were obtained using argon pressure and the observed stabilization may be explained by a positive volume of activation in the transition state leading to hydrogen release. Nanoconfinement in mesoporous silica, MCM-41, was investigated as alternative means to stabilize NH4BH4. However, other factors appear to significantly destabilize NH4BH4 and it rapidly decomposes at ambient temperatures into [(NH3)2BH2][BH4] (DADB) in accordance with the bulk reaction scheme. The hydrogen desorption kinetics from nanoconfined [(NH3)2BH2][BH4] is moderately enhanced as evidenced by a reduction in the DSC decomposition peak temperature of ΔT = -13 °C as compared to the bulk material. Finally, we note a surprising result, storage of DADB at temperature < -30 °C transformed, reversibly, the [(NH3)2BH2][BH4] into a new low temperature polymorph as revealed by both XRD and solid state MAS 11B MAS NMR. TA & AK are thankful for support from the US Department of Energy, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences & Biosciences. A portion of the research was performed using EMSL, a national scientific user facility sponsored by the Department of Energy's Office of Biological and Environmental Research and located at Pacific Northwest National Laboratory (PNNL). PNNL is operated by Battelle.

  5. Thermal Decomposition Behavior of Ammonium Perchlorate and of an Ammonium-Perchlorate-Based Composite Propellant

    NASA Technical Reports Server (NTRS)

    Behrens, R.; Minier, L.

    1998-01-01

    The thermal decomposition of ammonium perchlorate (AP) and ammonium-perchlorate-based composite propellants is studied using the simultaneous thermogravimetric modulated beam mass spectrometry (STMBMS) technique. The main objective of the present work is to evaluate whether the STMBMS can provide new data on these materials that will have sufficient detail on the reaction mechanisms and associated reaction kinetics to permit creation of a detailed model of the thermal decomposition process. Such a model is a necessary ingredient to engineering models of ignition and slow-cookoff for these AP-based composite propellants. Results show that the decomposition of pure AP is controlled by two processes. One occurs at lower temperatures (240 to 270 C), produces mainly H2O, O2, Cl2, N2O and HCl, and is shown to occur in the solid phase within the AP particles. 200(micro) diameter AP particles undergo 25% decomposition in the solid phase, whereas 20(micro) diameter AP particles undergo only 13% decomposition. The second process is dissociative sublimation of AP to NH3 + HClO4 followed by the decomposition of, and reaction between, these two products in the gas phase. The dissociative sublimation process occurs over the entire temperature range of AP decomposition, but only becomes dominant at temperatures above those for the solid-phase decomposition. AP-based composite propellants are used extensively in both small tactical rocket motors and large strategic rocket systems.

  6. The thermal decomposition behavior of ammonium perchlorate and of an ammonium-perchlorate-based composite propellant

    SciTech Connect

    Behrens, R.; Minier, L.

    1998-03-24

    The thermal decomposition of ammonium perchlorate (AP) and ammonium-perchlorate-based composite propellants is studied using the simultaneous thermogravimetric modulated beam mass spectrometry (STMBMS) technique. The main objective of the present work is to evaluate whether the STMBMS can provide new data on these materials that will have sufficient detail on the reaction mechanisms and associated reaction kinetics to permit creation of a detailed model of the thermal decomposition process. Such a model is a necessary ingredient to engineering models of ignition and slow-cookoff for these AP-based composite propellants. Results show that the decomposition of pure AP is controlled by two processes. One occurs at lower temperatures (240 to 270 C), produces mainly H{sub 2}O, O{sub 2}, Cl{sub 2}, N{sub 2}O and HCl, and is shown to occur in the solid phase within the AP particles. 200{micro} diameter AP particles undergo 25% decomposition in the solid phase, whereas 20{micro} diameter AP particles undergo only 13% decomposition. The second process is dissociative sublimation of AP to NH{sub 3} + HClO{sub 4} followed by the decomposition of, and reaction between, these two products in the gas phase. The dissociative sublimation process occurs over the entire temperature range of AP decomposition, but only becomes dominant at temperatures above those for the solid-phase decomposition. AP-based composite propellants are used extensively in both small tactical rocket motors and large strategic rocket systems.

  7. Stoichiometric analysis of ammonium nitrate and ammonium perchlorate with nanosecond laser induced breakdown spectroscopy

    NASA Astrophysics Data System (ADS)

    Sreedhar, S.; Rao, S. Venugopal; Kiran, P. Prem; Tewari, Surya P.; Kumar, G. Manoj

    2010-04-01

    We present our results on the stoichiometric analysis of ammonium nitrate (AN) and ammonium Perchlorate (AP) studied using laser induced breakdown spectroscopy (LIBS) with nanosecond pulses. The LIBS spectra collected for AP and AN, without any gating and using a high resolution spectrometer, exhibited characteristic lines corresponding to O, N, H, C, and K. The Oxygen line at 777.38 nm and three Nitrogen lines (N1, N2, N3) at 742.54 nm, 744.64 nm, 747.12 nm were used for evaluating the Oxygen/Nitrogen ratios. The intensities were calculated using area under the peaks and normalized to their respective transition probabilities and statistical weights. The O/N1 ratios estimated from the LIBS spectra were ~4.94 and ~5.11 for AP and O/N3 ratios were ~1.64 and ~1.47 for AN obtained from two independent measurements. The intensity ratios show good agreement with the actual stoichiometric ratios - four for AP and one for AN.

  8. Heterogeneous reactivity of chlorine atoms with ammonium sulfate and ammonium nitrate particles.

    PubMed

    Ciuraru, Raluca; Gosselin, Sylvie; Visez, Nicolas; Petitprez, Denis

    2012-04-01

    In this laboratory study, model particles of ammonium sulfate (AS) and ammonium nitrate (AN) were exposed to chlorine atoms and uptake experiments were performed in a coated wall flow tube reactor coupled to a molecular beam mass spectrometer. The reactive surfaces were prepared by coating the inner surface of the reactor using two different methods: either by depositing size-selected particles on the halocarbon wax or by spray depositing thin films using a constant output atomizer. The observed uptake coefficients vary for (NH(4))(2)SO(4), ranging from γ(Cl)(AS)≈ 1 × 10(-3) for size-selected particles to γ(Cl)(AS)≈ 6 × 10(-2) for thin films prepared by spray. An uptake coefficient of γ(Cl)(AN)≈ 2.5 × 10(-3) of Cl˙ on size-selected NH(4)NO(3) particles was measured. A heterogeneous recombination of Cl atoms to from Cl(2) molecules was observed for the two surfaces. Furthermore, an ageing process was observed for AS particles, this phenomenon leading to the formation of new chlorine species on the solid substrate. PMID:22374517

  9. Removal of ammonium from municipal landfill leachate using natural zeolites.

    PubMed

    Ye, Zhihong; Wang, Jiawen; Sun, Lingyu; Zhang, Daobin; Zhang, Hui

    2015-01-01

    Ammonium ion-exchange performance of the natural zeolite was investigated in both batch and column studies. The effects of zeolite dosage, contact time, stirring speed and pH on ammonium removal were investigated in batch experiments. The result showed that ammonium removal efficiency increased with an increase in zeolite dosage from 25 to 150 g/L, and an increase in stirring speed from 200 to 250 r/min. But further increase in zeolite dosage and stirring speed would result in an unpronounced increase of ammonium removal. The optimal pH for the removal of ammonium was found as 7.1. In the column studies, the effect of flow rate was investigated, and the total ammonium removal percentage during 180 min operation time decreased with the flow rate though the ion-exchange capacity varied to a very small extent with the flow rate ranging from 4 to 9 mL/min. The spent zeolite was regenerated by sodium chloride solution and the ammonia removal capacity of zeolite changed little or even increased after three regeneration cycles. PMID:26510611

  10. Anaerobic ammonium oxidation by anammox bacteria in the Black Sea

    NASA Astrophysics Data System (ADS)

    Kuypers, Marcel M. M.; Sliekers, A. Olav; Lavik, Gaute; Schmid, Markus; Jørgensen, Bo Barker; Kuenen, J. Gijs; Sinninghe Damsté, Jaap S.; Strous, Marc; Jetten, Mike S. M.

    2003-04-01

    The availability of fixed inorganic nitrogen (nitrate, nitrite and ammonium) limits primary productivity in many oceanic regions. The conversion of nitrate to N2 by heterotrophic bacteria (denitrification) is believed to be the only important sink for fixed inorganic nitrogen in the ocean. Here we provide evidence for bacteria that anaerobically oxidize ammonium with nitrite to N2 in the world's largest anoxic basin, the Black Sea. Phylogenetic analysis of 16S ribosomal RNA gene sequences shows that these bacteria are related to members of the order Planctomycetales performing the anammox (anaerobic ammonium oxidation) process in ammonium-removing bioreactors. Nutrient profiles, fluorescently labelled RNA probes, 15N tracer experiments and the distribution of specific `ladderane' membrane lipids indicate that ammonium diffusing upwards from the anoxic deep water is consumed by anammox bacteria below the oxic zone. This is the first time that anammox bacteria have been identified and directly linked to the removal of fixed inorganic nitrogen in the environment. The widespread occurrence of ammonium consumption in suboxic marine settings indicates that anammox might be important in the oceanic nitrogen cycle.

  11. Morphological evolution and visible light-induced degradation of Rhodamine 6G by nanocrystalline bismuth tungstate prepared using a template-based approach

    NASA Astrophysics Data System (ADS)

    Silva, Raissa Mendes; Batista Barbosa, Diego Augusto; de Jesus Silva Mendonça, Caritas; de Oliveira Lima, José Renato; Silva, Fernando Carvalho; Longo, Elson; Maciel, Adeilton Pereira; de Araujo Paschoal, Carlos William; Almeida, Marcio Aurélio Pinheiro

    2016-09-01

    The cleaning of water contaminated with organic dyes is a crucial problem nowadays. The search for good catalysts is intense, and bismuth tungstates have attracted a lot of attention because of their catalytic properties which are related to their crystal structure and morphology. In this study, we show that Bi2WO6 (BWO) crystals synthesized by the surfactant-assisted hydrothermal method create a different morphology than non-assisted crystals. With the assistance of the PVP surfactant, even the BWO crystalline structure could change, crystallizing into a high-symmetry metastable phase. These changes in morphology imply a decrease in BWO catalytic activity, which shows that insightful control of BWO synthesis is necessary to improve the BWO properties.

  12. PAPERS DEVOTED TO THE 90TH ANNIVERSARY OF A.M.PROKHOROV: Lasing properties of selectively pumped Raman-active Nd3+-doped molybdate and tungstate crystals

    NASA Astrophysics Data System (ADS)

    Basiev, Tasoltan T.; Doroshenko, Maxim E.; Ivleva, Lyudmila I.; Osiko, Vyacheslav V.; Kosmyna, M. B.; Komar', V. K.; Sulc, J.; Jelinkova, H.

    2006-08-01

    The lasing efficiency of Nd3+ ions is studied in laser materials capable of self-Raman frequency conversion. The lasing properties of tungstate and molybdate crystals with the scheelite structure (SrWO4, BaWO4, PbWO4, SrMoO4, PbMoO4) activated with neodymium ions are investigated upon longitudinal pumping by a 750-nm alexandrite laser or a 800-nm diode laser. The slope lasing efficiency obtained for a Nd3+:PbMoO4 laser emitting at 1054 nm is 54.3% for the total lasing efficiency of 46%, which is the best result for all the crystals with the scheelite structure studied so far. The simultaneous Q-switched lasing and self-Raman frequency conversion were demonstrated in neodymium-doped SrWO4, PbWO4, and BaWO4 crystals.

  13. Synthesis and characterization of a novel hybrid nano composite cation exchanger poly-o-toluidine Sn(IV) tungstate: Its analytical applications as ion-selective electrode

    NASA Astrophysics Data System (ADS)

    Khan, Asif Ali; Shaheen, Shakeeba

    2013-02-01

    A novel organic-inorganic nano composite cation exchanger poly-o-toluidine Sn(IV) tungstate has been synthesized by incorporation of a polymer material into inorganic precipitate. The material is a class of hybrid ion-exchanger with good ion-exchange properties, reproducibility, stability and good selectivity for heavy metals. The physico-chemical properties of this nano composite material were characterized by using XRD, TGA, FTIR, SEM and TEM. The ion-exchange capacity, pH titrations, elution behavior and chemical stability were also carried out to study ion-exchange properties of the material. Distribution studies for various metal ions revealed that the nano composite is highly selective for Cd(II). An ion-selective membrane electrode was fabricated using this material for the determination of Cd(II) ions in solutions. The analytical utility of this electrode was established by employing it as an indicator electrode in electrometric titrations.

  14. Synthesis, structural and vibrational studies on mixed alkali metal gadolinium double tungstate, K1-xNaxGd(WO4)2

    NASA Astrophysics Data System (ADS)

    Durairajan, A.; Thangaraju, D.; Moorthy Babu, S.

    2013-02-01

    Mixed alkali double tungstates K1-xNaxGd(WO4)2 (KNGW) (0 ⩽ x ⩽ 1) were synthesized by solid state reaction using sodium doped monoclinic KGd(WO4)2 (KGW). Synthesized KNGW powders were characterized using powder X-ray diffraction (XRD), differential thermal analysis (DTA), scanning electron microscopy (SEM) and Raman analysis. DTA analysis confirms that the melting point of the KGW matrix increases from 1063 °C to 1255 °C with increasing sodium content. The Powder XRD analyses reveal that mixed phases were observed up to 40 wt.% of Na in the KGW matrix above that percentage there is domination of scheelite structure in the synthesized powder. Polyhedral type, bi-pyramidal shape and spheroid shape morphology was observed for KGW, NKGW and NGW powders respectively. The Raman analysis was carried out to understand the vibrational characteristic changes with mixing of sodium ions in the KGW matrix.

  15. Ammonium inhibition of nitrogenase activity in Herbaspirillum seropedicae

    SciTech Connect

    Fu, H.; Burris, R.H. )

    1989-06-01

    The effect of oxygen, ammonium ion, and amino acids on nitrogenase activity in the root-associated N{sub 2}-fixing bacterium Herbaspirillum seropedicae was investigated in comparison with Azospirillum spp. and Rhodospirillum rubrum. H. seropedicae is microaerophilic, and its optimal dissolved oxygen level is from 0.04 to 0.2 kPa for dinitrogen fixation but higher when it is supplied with fixed nitrogen. No nitrogenase activity was detected when the dissolved O{sub 2} level corresponded to 4.0 kPa. Ammonium, a product of the nitrogenase reaction, reversible inhibited nitrogenase activity when added to derepressed cell cultures. However, the inhibition of nitrogenase activity was only partial even with concentrations of ammonium chloride as high as 20 mM. Amides such as glutamine and asparagine partially inhibited nitrogenase activity, but glutamate did not. Nitrogenase in crude extracts prepared from ammonium-inhibited cells showed activity as high as in extracts from N{sub 2}-fixing cells. The pattern of the dinitrogenase and the dinitrogenase reductase revealed by the immunoblotting technique did not change upon ammonium chloride treatment of cells in vivo. No homologous sequences were detected with the draT-draG probe from Azospirillum lipoferum. There is no clear evidence that ADP-ribosylation of the dinitrogenase reductase is involved in the ammonium inhibition of H. seropedicae. The uncoupler carbonyl cyanide m-chlorophenylhydrazone decreased the intracellular ATP concentration and inhibited the nitrogenase activity of whole cells. The ATP pool was significantly disturbed when cultures were treated with ammonium in vivo.

  16. Modeling of alkyl quaternary ammonium cations intercalated into montmorillonite lattice

    SciTech Connect

    Daoudi, El Mehdi; Boughaleb, Yahia; El Gaini, Layla; Meghea, Irina; Bakasse, Mina

    2013-05-15

    Highlights: ► The modification of montmorillonites by three surfactants increases the basal spacing. ► The model proposed show a bilayer conformation for the surfactant ODTMA. ► The DODMA and TOMA surfactants adopt a paraffin type arrangement. ► Behavior of surfactants in interlayer space was confirmed by TGA and ATR analysis. - Abstract: The objective of this work was to study the conformation of the quaternary ammonium cations viz., octadecyl trimethyl ammonium (ODTMA), dioctadecyl dimethyl ammonium (DMDOA) and trioctadecyl methyl ammonium (TOMA) intercalated within montmorillonite. The modified montmorillonite was characterized by X-ray diffraction in small angle (SAXS), thermal analysis (TGA) and infrared spectroscopy of attenuated total reflection (ATR). The modification of organophilic montmorillonites by the three surfactants ODTMA, DMDOA and TOMA increases the basal spacing from their respective intercalated distances of 1.9 nm, 2.6 nm and 3.4 nm respectively. The increase in the spacing due to the basic organic modification was confirmed by the results of thermal analysis (TGA) and infrared spectroscopy (ATR), and also supported by theoretical calculations of longitudinal and transversal chain sizes of these alkyl quaternary ammonium cations.

  17. Effects of bisphenol A on ammonium assimilation in soybean roots.

    PubMed

    Sun, Hai; Wang, Li Hong; Zhou, Qing; Huang, Xiao Hua

    2013-12-01

    Bisphenol A (BPA), which is ubiquitous in the environment, is an example of an endocrine-disrupting compound (EDC). Ammonium assimilation has an important function in plant growth and development. However, insufficient information on the potential effect of BPA on ammonium assimilation in plants is available. In this study, the effects of BPA on ammonium assimilation in roots of soybean seedlings were investigated. During the stress period, 1.5 mg L(-1) of BPA improved glutamine synthetase (GS)/glutamate synthase (GOGAT) cycle and glutamate dehydrogenase (GDH) pathway in ammonium assimilation. The amino acid and the soluble protein contents increased in the soybeans. At 17.2 and 50.0 mg L(-1) of BPA, the GS/GOGAT cycle was inhibited and the GDH pathway was promoted. The amino acid content increased and the soluble protein content decreased. During the recovery period, the GS/GOGAT cycle and the GDH pathway recovered at 1.5 and 17.2 mg L(-1) of BPA but not at 50.0 mg L(-1) of BPA. The amino acid content continuously increased and the soluble protein content decreased compared with those in the control treatment. In summary, BPA treatment could affect the contents of soluble protein and amino acid in the soybean roots by regulating ammonium assimilation. PMID:23649602

  18. Simultaneous removal of ammonium and suspended solids in multipurpose filters.

    PubMed

    Alkas, Deniz; Baykal, Bilsen Beler; Kinaci, Cumali

    2012-06-01

    A multipurpose filter in which sand and clinoptilolite are used together as filter material is suggested for the simultaneous removal of suspended solids and ammonium in one single unit. The capacity of the clinoptilolite used was determined as 10.4 mg/g for 20 mg/l initial ammonium concentration. In addition, a packed column ion exchanger with clinoptilolite and a classical sand filter were also investigated for comparison. Ammonium and suspended solids removal rates were observed and compared for all columns. The results of the column analysis have revealed that the ammonium removal rate, which was only 20% in the sand column, was increased to 100% by replacing 50% of the sand with clinoptilolite; similarly, the suspended solids removal, which was only 17% in the clinoptilolite column, was increased to 75% by replacing 50% of the clinoptilolite with sand. As such, when ion exchange and filtration processes were carried out in a multipurpose column, high removals for both parameters could be obtained simultaneously. Multipurpose columns could be an alternative both for the upgrading of existing treatment plants or for new plants for simultaneous removal of ammonium and suspended solids, giving considerable savings in terms of land requirements. PMID:22856296

  19. Electrospray Ionization Tandem Mass Spectrometry of Ammonium Cationized Polyethers

    NASA Astrophysics Data System (ADS)

    Nasioudis, Andreas; Heeren, Ron M. A.; van Doormalen, Irene; de Wijs-Rot, Nicolette; van den Brink, Oscar F.

    2011-05-01

    Quaternary ammonium salts (Quats) and amines are known to facilitate the MS analysis of high molar mass polyethers by forming low charge state adduct ions. The formation, stability, and behavior upon collision-induced dissociation (CID) of adduct ions of polyethers with a variety of Quats and amines were studied by electrospray ionization quadrupole time-of-flight, quadrupole ion trap, and linear ion trap tandem mass spectrometry (MS/MS). The linear ion trap instrument was part of an Orbitrap hybrid mass spectrometer that allowed accurate mass MS/MS measurements. The Quats and amines studied were of different degree of substitution, structure, and size. The stability of the adduct ions was related to the structure of the cation, especially the amine's degree of substitution. CID of singly/doubly charged primary and tertiary ammonium cationized polymers resulted in the neutral loss of the amine followed by fragmentation of the protonated product ions. The latter reveals information about the monomer unit, polymer sequence, and endgroup structure. In addition, the detection of product ions retaining the ammonium ion was observed. The predominant process in the CID of singly charged quaternary ammonium cationized polymers was cation detachment, whereas their doubly charged adduct ions provided the same information as the primary and tertiary ammonium cationized adduct ions. This study shows the potential of specific amines as tools for the structural elucidation of high molar mass polyethers.

  20. Removal of sulfur oxides from gas streams with ammonium sulfite

    SciTech Connect

    Spitz, A.W.

    1986-05-20

    A process is described for removal of sulfur oxides from sulfur oxide containing flue gases comprising scrubbing the flue gases in the first stage scrubber with an ammonium sulfite solution to remove most of the sulfur oxides and producing a liquor comprising ammonium sulfite, bisulfite and sulfate salts; recycling the liquor in the first state scrubber and producing a 40% to 50% solution of dissolved ammonium sulfite, bisulfite and sulfate salts in a first stage reservoir while maintaining the pH between about 5 and 5.8; maintaining the ratio of bisulfite to sulfite between approximately 2.3 to 1 and 1 to 1 without liberating ammonia; removing portions of the 40% to 50% solution of dissolved salts from the first stage reservoir; scrubbing the flue gases in a second stage scrubber with an ammonium sulfite solution of pH between 6.2 and 6.8 to remove additional sulfur oxides and producing a dilute liquor of 1% to 10% solids comprising ammonium sulfite, bisulfite and sulfate salts in a second stage reservoir; and pumping the dilute liquor from the second stage reservoir to the first stage reservoir in amounts sufficient to replace the removed portions.

  1. Loss of Fine Particle Ammonium from Denuded Nylon Filters

    SciTech Connect

    Yu, Xiao-Ying; Lee, Taehyoung; Ayres, Benjamin; Kreidenweis, Sonia M.; Malm, William C.; Collett, Jeffrey L.

    2006-08-01

    Ammonium is an important constituent of fine particulate mass in the atmosphere, but can be difficult to quantify due to possible sampling artifacts. Losses of semivolatile species such as NH4NO3 can be particularly problematic. In order to evaluate ammonium losses from aerosol particles collected on filters, a series of field experiments was conducted using denuded nylon and Teflon filters at Bondville, Illinois (February 2003), San Gorgonio, California (April 2003 and July 2004), Grand Canyon National Park, Arizona (May, 2003), Brigantine, New Jersey (November 2003), and Great Smoky Mountains National Park (NP), Tennessee (July–August 2004). Samples were collected over 24-hr periods. Losses from denuded nylon filters ranged from 10% (monthly average) in Bondville, Illinois to 28% in San Gorgonio, California in summer. Losses on individual sample days ranged from 1% to 65%. Losses tended to increase with increasing diurnal temperature and relative humidity changes and with the fraction of ambient total N(--III) (particulate NH4+ plus gaseous NH3) present as gaseous NH3. The amount of ammonium lost at most sites could be explained by the amount of NH4NO3 present in the sampled aerosol. Ammonium losses at Great Smoky Mountains NP, however, significantly exceeded the amount of NH4NO3 collected. Ammoniated organic salts are suggested as additional important contributors to observed ammonium loss at this location.

  2. Ammonium as a sustainable proton shuttle in bioelectrochemical systems.

    PubMed

    Cord-Ruwisch, Ralf; Law, Yingyu; Cheng, Ka Yu

    2011-10-01

    This work examines a pH control method using ammonium (NH(4)(+)) as a sustainable proton shuttle in a CEM-equipped BES. Current generation was sustained by adding NH(3) or ammonium hydroxide (NH(4)OH) to the anolyte, controlling its pH at 7. Ammonium ion migration maintained the catholyte pH at approximately 9.25. Such NH(4)(+)/NH(3) migration accounted for 90±10% of the ionic flux in the BES. Reintroducing the volatilized NH(3) from the cathode into the anolyte maintained a suitable anolyte pH for sustained microbial-driven current generation. Hence, NH(4)(+)/NH(3) acted as a proton shuttle that is not consumed in the process. PMID:21865037

  3. Exposure to common quaternary ammonium disinfectants decreases fertility in mice

    PubMed Central

    Melin, Vanessa E.; Potineni, Haritha; Hunt, Patricia; Griswold, Jodi; Siems, Bill; Werre, Stephen R.; Hrubec, Terry C.

    2014-01-01

    Quaternary ammonium compounds (QACs) are antimicrobial disinfectants commonly used in commercial and household settings. Extensive use of QACs results in ubiquitous human exposure, yet reproductive toxicity has not been evaluated. Decreased reproductive performance in laboratory mice coincided with the introduction of a disinfectant containing both alkyl dimethyl benzyl ammonium chloride (ADBAC) and didecyl dimethyl ammonium chloride (DDAC). QACs were detected in caging material over a period of several months following cessation of disinfectant use. Breeding pairs exposed for six months to a QAC disinfectant exhibited decreases in fertility and fecundity: increased time to first litter, longer pregnancy intervals, fewer pups per litter and fewer pregnancies. Significant morbidity in near term dams was also observed. In summary, exposure to a common QAC disinfectant mixture significantly impaired reproductive health in mice. This study illustrates the importance of assessing mixture toxicity of commonly used products whose components have only been evaluated individually. PMID:25483128

  4. Cetyltrimethyl ammonium bromide assisted hydrothermal growth of hematite hollow cubes

    SciTech Connect

    Wang, Wei-Wei; Yao, Jia-Liang

    2010-11-15

    Hematite hollow cubes have been prepared by forced hydrolysis of ferric chloride solutions under hydrothermal conditions. The effects of reaction time, reaction temperature and cetyltrimethyl ammonium bromide on the transformation process from akageneite to hematite were investigated in detail. The products were characterized by X-ray powder diffraction, scanning electron microscopy and transmission electron microscopy. It is found that cetyltrimethyl ammonium bromide was a critical factor influencing the phase transformation process of akageneite and the final morphology of the as-prepared products. With cetyltrimethyl ammonium bromide, hematite hollow cubes and porous spheres were obtained. Otherwise only dense cubes were observed even prolonging reaction time or increasing reaction temperature. The mechanism was proposed.

  5. Aerosol isotopic ammonium signatures over the remote Atlantic Ocean

    NASA Astrophysics Data System (ADS)

    Lin, C. T.; Jickells, T. D.; Baker, A. R.; Marca, A.; Johnson, M. T.

    2016-05-01

    We report aerosol ammonium 15N signatures for samples collected from research cruises on the South Atlantic and Caribbean using a new high sensitivity method. We confirm a pattern of isotopic signals from generally light (δ15N -5 to -10‰), for aerosols with very low (<2  nmol m-3) ammonium concentrations from the remote high latitude ocean, to generally heavier values (δ15N +5 to +10‰), for aerosols collected in temperate and tropical latitudes and with higher ammonium concentrations (>2  nmol m-3). We discuss whether this reflects a mixing of aerosols from two end-members (polluted continental and remote marine emissions), or isotopic fractionation during aerosol transport.

  6. Effect of temperature on ammonium removal in Scenedesmus sp.

    PubMed

    Ruiz-Martínez, A; Serralta, J; Seco, A; Ferrer, J

    2015-09-01

    The effect of temperature on microalgal ammonium uptake was investigated by carrying out four batch experiments in which a mixed culture of microalgae, composed mainly of Scenedesmus sp., was cultivated under different temperatures within the usual temperature working range in Mediterranean climate (15-34 °C). Ammonium removal rates increased with temperature up to 26 °C and stabilized thereafter. Ratkowsky and Cardinal temperatures models successfully reproduced the experimental data. Optimum (31.3 °C), minimum (8.8 °C) and maximum (46.1 °C) temperatures for ammonium removal by Scenedesmus sp. under the studied conditions were obtained as model parameters. These temperature-related parameters constitute very useful information for designing and operating wastewater treatment systems using these microalgae. PMID:26027902

  7. Handling of Ammonium Nitrate Mother-Liquid Radiochemical Production - 13089

    SciTech Connect

    Zherebtsov, Alexander; Dvoeglazov, Konstantine; Volk, Vladimir; Zagumenov, Vladimir; Zverev, Dmitriy; Tinin, Vasiliy; Kozyrev, Anatoly; Shamin, Dladimir; Tvilenev, Konstantin

    2013-07-01

    The aim of the work is to develop a basic technology of decomposition of ammonium nitrate stock solutions produced in radiochemical enterprises engaged in the reprocessing of irradiated nuclear fuel and fabrication of fresh fuel. It was necessary to work out how to conduct a one-step thermal decomposition of ammonium nitrate, select and test the catalysts for this process and to prepare proposals for recycling condensation. Necessary accessories were added to a laboratory equipment installation decomposition of ammonium nitrate. It is tested several types of reducing agents and two types of catalyst to neutralize the nitrogen oxides. It is conducted testing of modes of the process to produce condensation, suitable for use in the conversion of a new technological scheme of production. It is studied the structure of the catalysts before and after their use in a laboratory setting. It is tested the selected catalyst in the optimal range for 48 hours of continuous operation. (authors)

  8. Ammonium perchlorate structure and dynamics at low temperatures

    NASA Astrophysics Data System (ADS)

    Prask, H. J.; Choi, C. S.; Chesser, N. J.; Rosasco, G. J.

    1988-04-01

    Single-crystal and powder neutron diffraction, coherent neutron inelastic scattering, and Raman spectroscopy have been used to study the low temperature structure and dynamics of ammonium perchlorate. No evidence for a phase transition is found. Based on analysis of thermal motion amplitudes and inelastic neutron-scattering data for ND4ClO4 a Raman-active B3g symmetry zone-center mode at 45 cm-1 is identified as a libration. Another Raman-active mode, B1g symmetry at 33 cm-1, and a previously unobserved Au symmetry mode at 12 cm-1, are inferred to have significant librational character at q=0. Comparison of these results with earlier incoherent neutron scattering results suggests that, because of the low activation energy of ammonium ions, classical jump reorientations strongly influence ammonium-ion sublattice dynamics even to temperatures as low as 20 K. Partial dispersion curves are also presented.

  9. Steady state growth of E. Coli in low ammonium environment

    NASA Astrophysics Data System (ADS)

    Kim, Minsu; Deris, Barret; Zhang, Zhongge; Hwa, Terry

    2011-03-01

    Ammonium is the preferred nitrogen source for many microorganisms. In medium with low ammonium concentrations, enteric bacteria turn on the nitrogen responsive (ntr) genes to assimilate ammonium. Two proteins in E. coli, Glutamine synthetase (GS) and the Ammonium/methylammonium transporter AmtB play crucial roles in this regard. GS is the major ammonium assimilation enzyme below 1mM of NH4 + . AmtB is an inner membrane protein that transports NH4 + across the cell membrane against a concentration gradient. In order to study ammonium uptake at low NH4 + concentration at neutral pH, we developed a microfluidic flow chamber that maintains a homogenous nutrient environment during the course of exponential cell growth, even at very low concentration of nutrients. Cell growth can be accurately monitored using time-lapse microscopy. We followed steady state growth down to micro-molar range of NH4 + for the wild type and Δ amtB strains. The wild type strain is able to maintain the growth rate from 10mM down to a few uM of NH4 + , while the mutant exhibited reduced growth below ~ 20 ~uM of NH4 + . Simultaneous characterization of the expression levels of GS and AmtB using fluorescence reporters reveals that AmtB is turned on already at 1mM, but contributes to function only below ~ 30 ~uM in the wild-type. Down to ~ 20 ~uM of NH4 + , E.~coli can compensate the loss of AmtB by GS alone.

  10. Mutagenic activity of quaternary ammonium salt derivatives of carbohydrates.

    PubMed

    Dmochowska, Barbara; Sikora, Karol; Woziwodzka, Anna; Piosik, Jacek; Podgórska, Beata

    2016-01-01

    This paper presents a study on a series of quaternary ammonium salt (QAS) derivatives of glucopyranosides with an elongated hydrophobic hydrocarbon chain. The new N-[6-(β-D-glucopyranosyloxy)hexyl]ammonium bromides and their O-acetyl derivatives were analyzed via (1)H and (13)C NMR spectroscopy. The mutagenic activity of the newly synthesized QAS was investigated using two different techniques: The Vibrio harveyi luminescence assay and the Ames test. The obtained results support previous findings contesting QAS safety and indicate that QAS, specifically pyridinium derivatives, might be mutagenic. PMID:27559394

  11. Mutagenic activity of quaternary ammonium salt derivatives of carbohydrates

    PubMed Central

    Sikora, Karol; Woziwodzka, Anna; Piosik, Jacek; Podgórska, Beata

    2016-01-01

    Summary This paper presents a study on a series of quaternary ammonium salt (QAS) derivatives of glucopyranosides with an elongated hydrophobic hydrocarbon chain. The new N-[6-(β-D-glucopyranosyloxy)hexyl]ammonium bromides and their O-acetyl derivatives were analyzed via 1H and 13C NMR spectroscopy. The mutagenic activity of the newly synthesized QAS was investigated using two different techniques: The Vibrio harveyi luminescence assay and the Ames test. The obtained results support previous findings contesting QAS safety and indicate that QAS, specifically pyridinium derivatives, might be mutagenic. PMID:27559394

  12. A model of the spatial distribution of ammonium in precipitation

    SciTech Connect

    Liljestrand, H.M.

    1986-04-01

    The net acidity of precipitation depends on both acid and base contributions, with ammonia being one of the two major bases. A model of ammonium concentrations in precipitation is developed from estimates of the spatial and seasonal emission densities of NH/sub 3/ across the continental United States. Box models are used to determine the transport, reactions and distribution between gaseous and particulate phases. An acid-base scavenging model is developed to estimate area average ammonium concentrations in precipitation. Model predictions are compared with historical data.

  13. Tripropyl­ammonium trithio­cyanurate

    PubMed Central

    Yang, Yunxia

    2010-01-01

    In the title compound (systematic name: tripropyl­azanium 2,4,6-tris­ulfanyl­idene­cyclo­hexan-1-ide), (C3H7)3HN+·C3H2N3S3 −, one H atom of trithio­cyanuric acid is accepted by tripropyl­amine to form the ammonium ion. Coplanar trithio­cyanurate and tripropyl­ammonium ions [dihedral angle = 82.33 (8)°] form the salt, which is stabilised by various N—H⋯S and N—H⋯N contacts. PMID:21588990

  14. Quaternary Ammonium Disinfectant Issues Encountered in an Environmental Services Department.

    PubMed

    Boyce, John M; Sullivan, Linda; Booker, Arica; Baker, James

    2016-03-01

    We identified several factors affecting the use of quaternary ammonium-based (Quat) disinfectant in our facility. Microfiber wipers, cotton towels, and 1 of 2 types of disposable wipes soaked in a Quat disinfectant revealed significant binding of the disinfectant. Concentrations of Quat delivered by automated disinfectant dispensers varied widely. PMID:26821275

  15. Two types of ammonium uncoupling in pea chloroplasts.

    PubMed

    Opanasenko, V K; Vasyukhina, L A; Naydov, I A

    2010-06-01

    The effect of ammonium on ATP synthesis, electron transfer, and light-induced uptake of hydrogen ions in pea chloroplasts was studied. It is shown that the dependence of these reactions on ammonium concentration could be due to effects of two different uncoupling processes. The first process is induced by low ammonium concentrations (<0.2 mM); the second one is observed in the NH(4)Cl concentration interval of 0.5-5.0 mM. The first type of uncoupling is stimulated by palmitic acid or by N,N'-dicyclohexylcarbodiimide, while the second is stimulated by chloroplast thylakoid swelling caused by energy-dependent osmotic gradients. In the presence of the fluorescent dye sulforhodamine B, which does not penetrate through the cell membrane, this swelling causes the dye to enter the lumens. It is supposed that ammonium activates two different routes of cation leakage from the lumen. The first route involves channel proteins, while the second is a mechanosensitive pore that opens in response to osmotic gradients. PMID:20636271

  16. Growth rate dispersion of small ammonium alum crystals

    NASA Astrophysics Data System (ADS)

    Teodossiev, N.

    1987-01-01

    The growth rates of small (below 60 μm) and large (about 1 mm) crystals of ammonium alum was measured during batch crystallization from aqueous solutions. The growth rate distribution of small crystals is close to normal. With increasing supersaturation the growth rate of the large crystals increases more rapidly than that of small crystals.

  17. 40 CFR 180.473 - Glufosinate ammonium; tolerances for residues.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ..., pulp 0.20 Beet, sugar, molasses 5.0 Beet, sugar, roots 0.9 Beet, sugar, tops (leaves) 1.5 Bushberry... residues of the herbicide glufosinate-ammonium (butanoic acid, 2-amino-4-(hydroxymethylphosphinyl...-propionic acid, expressed as 2-amino-4-(hydroxymethylphosphinyl)butanoic acid equivalents, in or on...

  18. 40 CFR 180.473 - Glufosinate ammonium; tolerances for residues.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ..., roots 0.9 Beet, sugar, tops (leaves) 1.5 Bushberry subgroup 13B 0.15 Canola, meal 1.1 Canola, seed 0.40... is to be determined by measuring only the sum of glufosinate ammonium, 2-amino-4... 2-amino-4-(hydroxymethylphosphinyl)butanoic acid, in or on the commodity. Commodity Parts...

  19. Residual Particle Sizes of Evaporating Droplets: Ammonium Sulfate and Aldehydes

    NASA Astrophysics Data System (ADS)

    Sedehi, N.; Galloway, M. M.; De Haan, D. O.

    2012-12-01

    The reactions of carbonyls like glyoxal, methylglyoxal, and glycolaldehyde, with ammonium salts have been proposed as significant sources of atmospheric organic aerosol. Aerosol containing these compounds was generated in the laboratory using the Vibrating Orifice Aerosol Generator (VOAG). The particles were completely dried before they were measured using a SMPS system. The nonvolatile fraction of the resulting aerosol was measured. The drying times were varied between two and twenty minutes, and for ammonium sulfate and glyoxal reactions, minimum residual particle sizes were reached after 3.5 minutes. Reactions of glyoxal, glycolaldehyde, and methylglyoxal with ammonium sulfate appeared to have lower non-volatile fractions remaining at higher starting concentrations, suggesting that a constant 'excess volume,' likely water, was present in the residual particles that could not be evaporated even after 20 minutes of drying. These excess volumes were not observed in our previous experiments with aldehydes but no ammonium sulfate present. At the highest concentrations tested (100 uM), non-volatile fractions of aldehydes present in residual particles were 16 (±17) %, 41 (±28) %, and 17(±32) % for glyoxal, glycolaldehyde, and methylglyoxal, respectively.

  20. Producing ammonium sulfate from flue gas desulfurization by-products

    USGS Publications Warehouse

    Chou, I.-Ming; Bruinius, J.A.; Benig, V.; Chou, S.-F.J.; Carty, R.H.

    2005-01-01

    Emission control technologies using flue gas desulfurization (FGD) have been widely adopted by utilities burning high-sulfur fuels. However, these technologies require additional equipment, greater operating expenses, and increased costs for landfill disposal of the solid by-products produced. The financial burdens would be reduced if successful high-volume commercial applications of the FGD solid by-products were developed. In this study, the technical feasibility of producing ammonium sulfate from FGD residues by allowing it to react with ammonium carbonate in an aqueous solution was preliminarily assessed. Reaction temperatures of 60, 70, and 80??C and residence times of 4 and 6 hours were tested to determine the optimal conversion condition and final product evaluations. High yields (up to 83%) of ammonium sulfate with up to 99% purity were achieved under relatively mild conditions. The optimal conversion condition was observed at 60??C and a 4-hour residence time. The results of this study indicate the technical feasibility of producing ammonium sulfate fertilizer from an FGD by-product. Copyright ?? Taylor & Francis Inc.

  1. Biochemistry of growth inhibition by ammonium ions in mammalian cells

    SciTech Connect

    Ryll, T.; Valley, U.; Wagner, R. . Cell Culture Techniques Dept.)

    1994-06-20

    The intracellular pool of UDP-N-acetylglucosamine and UDP-N-acetylgalactosamine has been shown to act as a central target during the inhibitory action of ammonium ions in vitro cultivated mammalian cell cultures. This pool has been demonstrated to be elevated at the end of a batch cultivation and very quickly as a response to exogenously applied ammonium chloride by using four different cell lines (hybridoma, BHK, CHO, and Ltk-929). The amount of enlarged UDP aminohexoses is correlated to the inhibitor concentration and additionally dependent on the cell line. The formation of the UDP sugars is associated with a transient reduction of the UTP pool. Moreover, the quick formation of UDP-GNAC is strictly dependent on the presence of, glucose and ammonium. Both metabolites act as biochemical precursors. Additionally, the formation of UDP-GNAc after ammonium application has been shown to increase with an elevated cultivation pH and to be independent of the inhibition of transcription and translation processes. The intracellular amount of UDP-GNAc correlates with the level of growth inhibition in mammalian cell lines.

  2. 21 CFR 184.1296 - Ferric ammonium citrate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ferric ammonium citrate. 184.1296 Section 184.1296 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of Specific Substances Affirmed as GRAS...

  3. 21 CFR 184.1296 - Ferric ammonium citrate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ferric ammonium citrate. 184.1296 Section 184.1296 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS...

  4. 21 CFR 184.1296 - Ferric ammonium citrate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ferric ammonium citrate. 184.1296 Section 184.1296 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of Specific Substances Affirmed as GRAS...

  5. 21 CFR 184.1296 - Ferric ammonium citrate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ferric ammonium citrate. 184.1296 Section 184.1296 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of Specific Substances Affirmed...

  6. GRANULATION OF COMPLEX FERTILIZERS CONTAINING AMMONIUM SULFATE BY MELT TECHNOLOGY

    EPA Science Inventory

    A novel process was developed for production of high analysis fertilizers in which large portions of the nutrients are derived from by-product and waste ammonium sulfate. The materials produced exhibit good physical and storage characteristics and are similar in grades to those n...

  7. Glufosinate and Ammonium Sulfate Inhibits Atrazine Degradation in Adapted Soils

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The co-application of glufosinate with nitrogen fertilizers may alter atrazine co-metabolism, thereby extending the herbicide’s residual weed control in adapted soils. The objective of this study was to assess the effects of glufosinate, ammonium sulfate, and the combination of glufosinate and ammo...

  8. Salmonella enterica Strains with Reduced Susceptibility to Quarternary Ammonium Compounds

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Background: Salmonella spp. are responsible for 76 million illnesses per year in the U.S. Quaternary ammonium compounds (QAC) are commonly used antimicrobial agents. Reduced susceptibility to these compounds by a broad spectrum of organisms is a concern. Methods: Salmonella enterica strains with r...

  9. Weed control efficacy with ammonium nonanoate for organic vegetable production

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Precision application of herbicides is important to vegetable producers because of the limited number of herbicides available and the potential for crop injury. Racer® (ammonium nonanoate) is a contact herbicide labeled for food use and is now labeled as a bio-herbicide for organically grown food c...

  10. Aqueous ammonia and ammonium chloride hydrates: Principal infrared spectra

    NASA Astrophysics Data System (ADS)

    Max, Jean-Joseph; Chapados, Camille

    2013-08-01

    The infrared (IR) spectra of aqueous ammonia (NH3) and aqueous ammonium chloride (NH4Cl) were recorded by attenuated total reflectance to obtain their molecular organizations. Factor analysis (FA) of the spectra revealed two hydrates for each species: (NH3)2ṡH2O and NH3ṡ3H2O; NH·HO; and (NH4+,Cl)·3HO, respectively. The hydrate spectra and species abundances were obtained as a function of total concentrations. From this the equilibrium equation between the two ammonia hydrates was determined: 2[(NH)2·HO]+5(HO)2⇌4[NH·3HO] with its equilibrium constant Kα = (2.3 ± 0.6) × 10-5 L3 mol-3. Similarly, for the two ammonium chloride hydrates the equation is 2[(NHCl)2·HO]+5(HO)2⇌4[NHCl·3HO] with its equilibrium constant: Kβ = (4 ± 1) × 10-7 L3 mol-3. Band simulations of the hydrate spectra were compared to that of pure liquid water and parent molecules. For aqueous ammonium chloride solutions the water and all ammonium hydrate bands are slightly displaced from that of pure water and pure ammonium chloride, respectively. However, for ammonia hydrates the situation is different: compared to the gas situation the hydrate water bands have similar displacements as that of pure liquid water; the ammonia deformation bands are also little displaced but the stretching bands are strongly red shifted. These shifts, which are even greater than that in pure liquid water, are attributed to strong hydrogen bonding situations: water-H with N-ammonia and ammonia-H with O-water. This explains the high solubility of ammonia in water. The comparison between the spectra of aqueous ammonium chloride and ammonia hydrates indicates that ammonium ion is not present in aqueous ammonia from 11.3 M down to at least our detection limit of 3 mM NH3.

  11. Structure, hydrogen bonding and thermal expansion of ammonium carbonate monohydrate.

    PubMed

    Fortes, A Dominic; Wood, Ian G; Alfè, Dario; Hernández, Eduardo R; Gutmann, Matthias J; Sparkes, Hazel A

    2014-12-01

    We have determined the crystal structure of ammonium carbonate monohydrate, (NH4)2CO3·H2O, using Laue single-crystal diffraction methods with pulsed neutron radiation. The crystal is orthorhombic, space group Pnma (Z = 4), with unit-cell dimensions a = 12.047 (3), b = 4.453 (1), c = 11.023 (3) Å and V = 591.3 (3) Å(3) [ρcalc = 1281.8 (7) kg m(-3)] at 10 K. The single-crystal data collected at 10 and 100 K are complemented by X-ray powder diffraction data measured from 245 to 273 K, Raman spectra measured from 80 to 263 K and an athermal zero-pressure calculation of the electronic structure and phonon spectrum carried out using density functional theory (DFT). We find no evidence of a phase transition between 10 and 273 K; above 273 K, however, the title compound transforms first to ammonium sesquicarbonate monohydrate and subsequently to ammonium bicarbonate. The crystallographic and spectroscopic data and the calculations reveal a quite strongly hydrogen-bonded structure (EHB ≃ 30-40 kJ mol(-1)), on the basis of H...O bond lengths and the topology of the electron density at the bond critical points, in which there is no free rotation of the ammonium cation at any temperature. The barrier to free rotation of the ammonium ions is estimated from the observed librational frequency to be ∼ 36 kJ mol(-1). The c-axis exhibits negative thermal expansion, but the thermal expansion behaviour of the a and b axes is ormal. PMID:25449618

  12. Structure, hydrogen bonding and thermal expansion of ammonium carbonate monohydrate

    PubMed Central

    Fortes, A. Dominic; Wood, Ian G.; Alfè, Dario; Hernández, Eduardo R.; Gutmann, Matthias J.; Sparkes, Hazel A.

    2014-01-01

    We have determined the crystal structure of ammonium carbonate monohydrate, (NH4)2CO3·H2O, using Laue single-crystal diffraction methods with pulsed neutron radiation. The crystal is orthorhombic, space group Pnma (Z = 4), with unit-cell dimensions a = 12.047 (3), b = 4.453 (1), c = 11.023 (3) Å and V = 591.3 (3) Å3 [ρcalc = 1281.8 (7) kg m−3] at 10 K. The single-crystal data collected at 10 and 100 K are complemented by X-ray powder diffraction data measured from 245 to 273 K, Raman spectra measured from 80 to 263 K and an athermal zero-pressure calculation of the electronic structure and phonon spectrum carried out using density functional theory (DFT). We find no evidence of a phase transition between 10 and 273 K; above 273 K, however, the title compound transforms first to ammonium sesquicarbonate monohydrate and subsequently to ammonium bicarbonate. The crystallographic and spectroscopic data and the calculations reveal a quite strongly hydrogen-bonded structure (E HB ≃ 30–40 kJ mol−1), on the basis of H⋯O bond lengths and the topology of the electron density at the bond critical points, in which there is no free rotation of the ammonium cation at any temperature. The barrier to free rotation of the ammonium ions is estimated from the observed librational frequency to be ∼ 36 kJ mol−1. The c-axis exhibits negative thermal expansion, but the thermal expansion behaviour of the a and b axes is ormal. PMID:25449618

  13. 40 CFR 721.9075 - Quaternary ammonium salt of fluorinated alkylaryl amide.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Quaternary ammonium salt of... New Uses for Specific Chemical Substances § 721.9075 Quaternary ammonium salt of fluorinated alkylaryl... identified generically as quaternary ammonium salt of fluorinated alkylaryl amide (PMN No. P-92-688)...

  14. 40 CFR 721.9075 - Quaternary ammonium salt of fluorinated alkylaryl amide.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Quaternary ammonium salt of... New Uses for Specific Chemical Substances § 721.9075 Quaternary ammonium salt of fluorinated alkylaryl... identified generically as quaternary ammonium salt of fluorinated alkylaryl amide (PMN No. P-92-688)...

  15. 40 CFR 721.10100 - Dialkyl dimethyl ammonium carbonate (2:1) (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Dialkyl dimethyl ammonium carbonate (2... Specific Chemical Substances § 721.10100 Dialkyl dimethyl ammonium carbonate (2:1) (generic). (a) Chemical... as dialkyl dimethyl ammonium carbonate (2:1) (PMN P-03-716) is subject to reporting under...

  16. 40 CFR 721.10479 - Quaternary ammonium compounds, tris(hydrogenated tallow alkyl)methyl, chlorides.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Quaternary ammonium compounds, tris... SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10479 Quaternary ammonium compounds... subject to reporting. (1) The chemical substance identified as quaternary ammonium compounds,...

  17. 40 CFR 721.8658 - Modified polymer of vinyl acetate and quaternary ammonium compound (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... quaternary ammonium compound (generic). 721.8658 Section 721.8658 Protection of Environment ENVIRONMENTAL... quaternary ammonium compound (generic). (a) Chemical substance and significant new uses subject to reporting... ammonium compound (PMN P-99-0874) is subject to reporting under this section for the significant new...

  18. 40 CFR 721.8658 - Modified polymer of vinyl acetate and quaternary ammonium compound (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... quaternary ammonium compound (generic). 721.8658 Section 721.8658 Protection of Environment ENVIRONMENTAL... quaternary ammonium compound (generic). (a) Chemical substance and significant new uses subject to reporting... ammonium compound (PMN P-99-0874) is subject to reporting under this section for the significant new...

  19. 40 CFR 721.10479 - Quaternary ammonium compounds, tris(hydrogenated tallow alkyl)methyl, chlorides.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Quaternary ammonium compounds, tris... SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10479 Quaternary ammonium compounds... subject to reporting. (1) The chemical substance identified as quaternary ammonium compounds,...

  20. 40 CFR 721.8658 - Modified polymer of vinyl acetate and quaternary ammonium compound (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... quaternary ammonium compound (generic). 721.8658 Section 721.8658 Protection of Environment ENVIRONMENTAL... quaternary ammonium compound (generic). (a) Chemical substance and significant new uses subject to reporting... ammonium compound (PMN P-99-0874) is subject to reporting under this section for the significant new...

  1. 40 CFR 721.10342 - Quaternary ammonium compounds, fatty alkyl dialkyl hydroxide (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Quaternary ammonium compounds, fatty... Significant New Uses for Specific Chemical Substances § 721.10342 Quaternary ammonium compounds, fatty alkyl... chemical substance identified generically as quaternary ammonium compounds, fatty alkyl dialkyl...

  2. 40 CFR 721.10342 - Quaternary ammonium compounds, fatty alkyl dialkyl hydroxide (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Quaternary ammonium compounds, fatty... Significant New Uses for Specific Chemical Substances § 721.10342 Quaternary ammonium compounds, fatty alkyl... chemical substance identified generically as quaternary ammonium compounds, fatty alkyl dialkyl...

  3. 40 CFR 721.8658 - Modified polymer of vinyl acetate and quaternary ammonium compound (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... quaternary ammonium compound (generic). 721.8658 Section 721.8658 Protection of Environment ENVIRONMENTAL... quaternary ammonium compound (generic). (a) Chemical substance and significant new uses subject to reporting... ammonium compound (PMN P-99-0874) is subject to reporting under this section for the significant new...

  4. 40 CFR 721.10342 - Quaternary ammonium compounds, fatty alkyl dialkyl hydroxide (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Quaternary ammonium compounds, fatty... Significant New Uses for Specific Chemical Substances § 721.10342 Quaternary ammonium compounds, fatty alkyl... chemical substance identified generically as quaternary ammonium compounds, fatty alkyl dialkyl...

  5. 40 CFR 721.10443 - Ethoxylated alkylphenol sulfate, ammonium salt (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ..., ammonium salt (generic). 721.10443 Section 721.10443 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.10443 Ethoxylated alkylphenol sulfate, ammonium salt... identified generically as ethoxylated alkylphenol sulfate, ammonium salt (PMN P-01-470) is subject...

  6. 40 CFR 721.10170 - Polyoxyethylene polyalkylarylphenylether sulfate ammonium salt (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... polyalkylarylphenylether sulfate ammonium salt (generic). 721.10170 Section 721.10170 Protection of Environment... polyalkylarylphenylether sulfate ammonium salt (generic). (a) Chemical substance and significant new uses subject to... sulfate ammonium salt (PMN P-03-197) is subject to reporting under this section for the significant...

  7. 40 CFR 721.9075 - Quaternary ammonium salt of fluorinated alkylaryl amide.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Quaternary ammonium salt of... New Uses for Specific Chemical Substances § 721.9075 Quaternary ammonium salt of fluorinated alkylaryl... identified generically as quaternary ammonium salt of fluorinated alkylaryl amide (PMN No. P-92-688)...

  8. 40 CFR 721.9075 - Quaternary ammonium salt of fluorinated alkylaryl amide.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Quaternary ammonium salt of... New Uses for Specific Chemical Substances § 721.9075 Quaternary ammonium salt of fluorinated alkylaryl... identified generically as quaternary ammonium salt of fluorinated alkylaryl amide (PMN No. P-92-688)...

  9. 40 CFR 721.9075 - Quaternary ammonium salt of fluorinated alkylaryl amide.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Quaternary ammonium salt of... New Uses for Specific Chemical Substances § 721.9075 Quaternary ammonium salt of fluorinated alkylaryl... identified generically as quaternary ammonium salt of fluorinated alkylaryl amide (PMN No. P-92-688)...

  10. 40 CFR 721.10170 - Polyoxyethylene polyalkylarylphenylether sulfate ammonium salt (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... polyalkylarylphenylether sulfate ammonium salt (generic). 721.10170 Section 721.10170 Protection of Environment... polyalkylarylphenylether sulfate ammonium salt (generic). (a) Chemical substance and significant new uses subject to... sulfate ammonium salt (PMN P-03-197) is subject to reporting under this section for the significant...

  11. 40 CFR 721.10170 - Polyoxyethylene polyalkylarylphenylether sulfate ammonium salt (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... polyalkylarylphenylether sulfate ammonium salt (generic). 721.10170 Section 721.10170 Protection of Environment... polyalkylarylphenylether sulfate ammonium salt (generic). (a) Chemical substance and significant new uses subject to... sulfate ammonium salt (PMN P-03-197) is subject to reporting under this section for the significant...

  12. 40 CFR 721.10170 - Polyoxyethylene polyalkylarylphenylether sulfate ammonium salt (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... polyalkylarylphenylether sulfate ammonium salt (generic). 721.10170 Section 721.10170 Protection of Environment... polyalkylarylphenylether sulfate ammonium salt (generic). (a) Chemical substance and significant new uses subject to... sulfate ammonium salt (PMN P-03-197) is subject to reporting under this section for the significant...

  13. 40 CFR 721.10170 - Polyoxyethylene polyalkylarylphenylether sulfate ammonium salt (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... polyalkylarylphenylether sulfate ammonium salt (generic). 721.10170 Section 721.10170 Protection of Environment... polyalkylarylphenylether sulfate ammonium salt (generic). (a) Chemical substance and significant new uses subject to... sulfate ammonium salt (PMN P-03-197) is subject to reporting under this section for the significant...

  14. Anaerobic ammonium oxidation, denitrification and dissimilatory nitrate reduction to ammonium in the East China Sea sediment

    NASA Astrophysics Data System (ADS)

    Song, G. D.; Liu, S. M.; Marchant, H.; Kuypers, M. M. M.; Lavik, G.

    2013-03-01

    Benthic nitrogen transformation pathways were investigated in the sediment of the East China Sea in June of 2010 using the 15N isotope pairing technique. Slurry incubations indicated that denitrification, anammox and dissimilatory nitrate reduction to ammonium (DNRA) as well as nitrate release by nitrate storing organisms occurred in the East China Sea sediments. These four processes did not exist independently, the nitrate release therefore diluted the 15N labeling fraction of NO3-, a part of the 15NH4+ derived from DNRA also formed 30N2 via anammox. Therefore current methods of rate calculations led to over and underestimations of anammox and denitrification respectively. Following the procedure outlined in Thampdrup and Dalsgaard (2002), denitrification rates were slightly underestimated by on average 6% without regard to the effect of nitrate release, while this underestimation could be counteracted by the presence of DNRA. On the contrary, anammox rates calculated from 15NO3- experiment were significantly overestimated by 42% without considering nitrate release. In our study this overestimation could only be compensated 14% by taking DNRA into consideration. In a parallel experiment amended with 15NH4+ + 14NO3-, anammox rates were not significantly influenced by DNRA due to the high background of 15NH4+ addition. Excluding measurements in which bioirrigation was present, integrated denitrification rates decreased from 10 to 4 mmol N m-2 d-1 with water depth, while integrated anammox rates increased from 1.5 to 4.0 mmol N m-2 d-1. Consequently, the relative contribution of anammox to the total N-loss increased from 13% at the shallowest site near the Changjiang estuary to 50% at the deepest site on the outer shelf. This study represents the first time in which anammox has been demonstrated to play a significant role in benthic nitrogen cycling in the East China Sea sediment, especially on the outer shelf. N-loss as N2 was the main pathway

  15. Tunable quasi-cw two-micron lasing in diode-pumped crystals of mixed Tm{sup 3+}-doped sodium - lanthanum - gadolinium molybdates and tungstates

    SciTech Connect

    Bol'shchikov, F A; Ryabochkina, P A; Zharikov, Evgeny V; Lis, Denis A; Subbotin, Kirill A; Zakharov, N G; Antipov, Oleg L

    2010-12-09

    Two-micron lasing is obtained for the first time on the {sup 3}F{sub 4} {yields} {sup 3}H{sub 6} transition of Tm{sup 3+} ions in diode-pumped crystals of mixed sodium - lanthanum - gadolinium tungstate Tm:NaLa{sub 1/2}Gd{sub 1/2}(WO{sub 4}){sub 2} (C{sub Tm} = 3.6 at %) (3.6Tm : NLGW) and molybdate Tm:NaLa{sub 1/3}Gd{sub 2/3}(MoO{sub 4}){sub 2} (C{sub Tm} = 4.8 at %) (4.8Tm : NLGM). For the 3.6Tm : NLGW crystal, the quasi-cw laser output power exceeded 200 mW and the slope efficiency (with respect to absorbed pump power) for the {pi}- and {sigma}-polarisations at wavelengths of 1908 and 1918 nm was 34% and 30%, respectively. The laser wavelength of this crystal was continuously tuned within the spectral range of 1860 - 1935 nm. For the 4.8Tm : NLGM crystal, the slope efficiency for the {pi}- and {sigma}-polarisations at wavelengths of 1910 and 1918 nm was 27% and 23%, respectively, and the laser wavelength was tunable within the spectral range of 1870 - 1950 nm. (lasers)

  16. The Measurement of Hot-Spots in Granulated Ammonium Nitrate

    NASA Astrophysics Data System (ADS)

    Proud, W. G.

    2002-07-01

    Ammonium Nitrate (AN) is one of the components of the most widely used explosive in the world namely, ammonium nitrate: fuel oil mixtures (ANFO). By itself, it is an oxygen positive explosive with a large critical diameter. Hot-spots are produced in explosives by various means including gas space collapse, localised shear or friction. If these hot-spots reach critical conditions of size, temperature and duration reaction can grow. This deflagration stage may eventually transition to detonation. This paper describes high-speed image-intensified photography study in which the number and growth of hot spots in granular AN are monitored for a range of different impact pressures. The results can be used in detonation codes to provide a more accurate and realistic description of the initiation process.

  17. The Measurement of Hot-spots in Granulated Ammonium Nitrate

    NASA Astrophysics Data System (ADS)

    Proud, William; Field, John

    2001-06-01

    Ammonium Nitrate (AN) is one of the components of the most widely used explosive in the world ammonium nitrate: fuel oil mixtures (ANFO). By itself, it is an oxygen negative explosive with a large critical diameter. Hot-spots are produced in explosives by various means including gas space collapse, localised shear or friction. If these hot-spots reach critical conditions of size, temperature and duration size reaction can grow. This deflagration stage may eventually transition to detonation. This paper describes a system and presents results where high-speed image intensified photography is used to monitor the number and growth of hot spots in granular AN under a range of different impact pressures. The results can be used in detonation codes to provide a more accurate and realistic description of the initiation process.

  18. Modified quaternary ammonium salts as potential antimalarial agents.

    PubMed

    Basilico, Nicoletta; Migotto, Mara; Ilboudo, Denise Patoinewende; Taramelli, Donatella; Stradi, Riccardo; Pini, Elena

    2015-08-01

    A series of new quaternary ammonium salts containing a polyconjugated moiety has been synthesized and characterized; their biological activity as potential antimalarial agents was investigated, as well. All compounds were screened against chloroquine resistant W-2 (CQ-R) and chloroquine sensitive, D-10 (CQ-S) strains of Plasmodium falciparum showing IC50 in the submicromolar range and low toxicity against human endothelial cells. PMID:26081764

  19. New solid electrolytes: substituted organic ammonium silver iodides

    SciTech Connect

    Ferraro, J.R.; Walling, P.L.; Sherren, A.T.

    1980-01-01

    Several new solid electrolytes were synthesized from the reaction of substituted organic ammonium hydroiodides (pyridinium and quinolinium type) and varying quantities of silver iodide. The inductive effects of nucleophilic and electrophilic substitution on the pyridinium or quinolinium ring, as well as substituent position on the ionic conductivity, were determined. Pressure and thermal studies were undertaken to determine if new nonambient conductive phases existed. 39 references, 4 figures, 2 tables.

  20. Ammonium photo-production by heterocytous cyanobacteria: potentials and constraints.

    PubMed

    Grizeau, Dominique; Bui, Lan Anh; Dupré, Catherine; Legrand, Jack

    2016-08-01

    Over the last decades, production of microalgae and cyanobacteria has been developed for several applications, including novel foods, cosmetic ingredients and more recently biofuel. The sustainability of these promising developments can be hindered by some constraints, such as water and nutrient footprints. This review surveys data on N2-fixing cyanobacteria for biomass production and ways to induce and improve the excretion of ammonium within cultures under aerobic conditions. The nitrogenase complex is oxygen sensitive. Nevertheless, nitrogen fixation occurs under oxic conditions due to cyanobacteria-specific characteristics. For instance, in some cyanobacteria, the vegetative cell differentiation in heterocyts provides a well-adapted anaerobic microenvironment for nitrogenase protection. Therefore, cell cultures of oxygenic cyanobacteria have been grown in laboratory and pilot photobioreactors (Dasgupta et al., 2010; Fontes et al., 1987; Moreno et al., 2003; Nayak & Das, 2013). Biomass production under diazotrophic conditions has been shown to be controlled by environmental factors such as light intensity, temperature, aeration rate, and inorganic carbon concentration, also, more specifically, by the concentration of dissolved oxygen in the culture medium. Currently, there is little information regarding the production of extracellular ammonium by heterocytous cyanobacteria. This review compares the available data on maximum ammonium concentrations and analyses the specific rate production in cultures grown as free or immobilized filamentous cyanobacteria. Extracellular production of ammonium could be coupled, as suggested by recent research on non-diazotrophic cyanobacteria, to that of other high value metabolites. There is little information available regarding the possibility for using diazotrophic cyanobacteria as cellular factories may be in regard of the constraints due to nitrogen fixation. PMID:25613641

  1. Nanomodified vermiculite NMV - a new material for recycling ammonium nitrogen

    NASA Astrophysics Data System (ADS)

    Rama, Miradije; Laiho, Taina; Eklund, Olav; Lehto, Kirsi; Shebanov, Alex; Smått, Jan-Henrik

    2016-04-01

    Vermiculites ((Mg,Fe,Al)3(Al,Si)4O10(OH)24H2O) are naturally occurring minerals from hydromica group with a high cation exchange capacity and large surface area. Since vermiculite is a hydrated mineral, its structure can be changed with heat. In this study vermiculite samples were heated in an oven until the interlayer distance of them diminished from 14 Å to 11.7 Å. This method for improving vermiculites intake of ammonium ions by heating, is an invention made at the University of Turku. Nanomodified vermiculite (NMV) is able to absorb up to 4.7 wt% of ammonium. NMV can be used as an efficient filter and immobilizer of ammonium in different environments. NMV has been efficiently tested on waste water from a biogas plant, human urine, combustion experiments, industrial chimneys, excrements from farms etc. Ammonium doped vermiculite (ADV) is further developed for fertilizer use. Performed experiments have testified the usability of ADV as a fertilizer. At first step the NMV was processed with the reject water from a biogas plant, were it absorbed NH4+ into the lattice. At second, the ADV was used as nutrient source for garden plants. Geraniums and begonias were used as test plants of the work. Plant growth rate was evaluated based on plant weight. Results showed that significant increase of the growth of geraniums and of begonias were observed when comparing to those cultivations where plants have got normal fertilization. Moreover, ADV has been tested as a fertilizer in greenhouse experiments with spruces and pines. After five months, the weight of the plants that had grown in a substrate containing ADV was 10 times the weight of plants growing in the reference substrate.

  2. Nitrogen Addition Regulates Soil Nematode Community Composition through Ammonium Suppression

    PubMed Central

    Wei, Cunzheng; Zheng, Huifen; Li, Qi; Lü, Xiaotao; Yu, Qiang; Zhang, Haiyang; Chen, Quansheng; He, Nianpeng; Kardol, Paul; Liang, Wenju; Han, Xingguo

    2012-01-01

    Nitrogen (N) enrichment resulting from anthropogenic activities has greatly changed the composition and functioning of soil communities. Nematodes are one of the most abundant and diverse groups of soil organisms, and they occupy key trophic positions in the soil detritus food web. Nematodes have therefore been proposed as useful indicators for shifts in soil ecosystem functioning under N enrichment. Here, we monitored temporal dynamics of the soil nematode community using a multi-level N addition experiment in an Inner Mongolia grassland. Measurements were made three years after the start of the experiment. We used structural equation modeling (SEM) to explore the mechanisms regulating nematode responses to N enrichment. Across the N enrichment gradient, significant reductions in total nematode abundance, diversity (H' and taxonomic richness), maturity index (MI), and the abundance of root herbivores, fungivores and omnivores-predators were found in August. Root herbivores recovered in September, contributing to the temporal variation of total nematode abundance across the N gradient. Bacterivores showed a hump-shaped relationship with N addition rate, both in August and September. Ammonium concentration was negatively correlated with the abundance of total and herbivorous nematodes in August, but not in September. Ammonium suppression explained 61% of the variation in nematode richness and 43% of the variation in nematode trophic group composition. Ammonium toxicity may occur when herbivorous nematodes feed on root fluid, providing a possible explanation for the negative relationship between herbivorous nematodes and ammonium concentration in August. We found a significantly positive relationship between fungivores and fungal phospholipid fatty acids (PLFA), suggesting bottom-up control of fungivores. No such relationship was found between bacterivorous nematodes and bacterial PLFA. Our findings contribute to the understanding of effects of N enrichment in

  3. Relevance of ammonium oxidation within biological soil crust communities

    USGS Publications Warehouse

    Johnson, S.L.; Budinoff, C.R.; Belnap, J.; Garcia-Pichel, F.

    2005-01-01

    Thin, vertically structured topsoil communities that become ecologically important in arid regions (biological soil crusts or BSCs) are responsible for much of the nitrogen inputs into pristine arid lands. We studied N2 fixation and ammonium oxidation (AO) at subcentimetre resolution within BSCs from the Colorado Plateau. Pools of dissolved porewater nitrate/ nitrite, ammonium and organic nitrogen in wetted BSCs were high in comparison with those typical of aridosoils. They remained stable during incubations, indicating that input and output processes were of similar magnitude. Areal N2 fixation rates (6.5-48 ??mol C2H2 m-2 h -1) were high, the vertical distribution of N2 fixation peaking close to the surface if populations of heterocystous cyanobacteria were present, but in the subsurface if they were absent. Areal AO rates (19-46 ??mol N m-2 h-1) were commensurate with N2 fixation inputs. When considering oxygen availability, AO activity invariably peaked 2-3 mm deep and was limited by oxygen (not ammonium) supply. Most probable number (MPN)-enumerated ammonia-oxidizing bacteria (6.7-7.9 ?? 103 cells g-1 on average) clearly peaked at 2-3 mm depth. Thus, AO (hence nitrification) is a spatially restricted but important process in the nitrogen cycling of BSC, turning much of the biologically fixed nitrogen into oxidized forms, the fate of which remains to be determined.

  4. Production of ammonium sulfate fertilizer from FGD-gypsum

    SciTech Connect

    Chou, M.I.M.; Rostam-Abadi, M.; Li, Y.C.

    1995-12-31

    The overall goal of this study is to assess the technical and economic feasibilities for producing marketable products including fertilizer-grade ammonium sulfate from gypsum produced as part of lime/limestone flue gas desulfurization (FGD) processes. Millions of tone of FGD-gypsum by-product may be produced in this decade as a result of the 1990 Clean Air Act Amendments. In this research, bench-scale experiments were conducted to obtain process data for the production of ammonium sulfate from FGD-gypsum and to help evaluate technical and economic feasibilities of the process. The FGD-gypsum sample produced from a Chiyoda Thoroughbred 121-FGD process installed on the Abbott power plant in Champaign, EL which was composed of 98.36% gypsum (CaSO{sub 4}{sm_bullet}2H{sub 2}O) and less than 0.01% calcium sulfite (CaSO) was used. The preliminary results of bench-scale experiments to evaluate the influence of reaction conditions to produce ammonium sulfate from FGD-gypsum are presented in this paper.

  5. Structural basis for Mep2 ammonium transceptor activation by phosphorylation

    PubMed Central

    van den Berg, Bert; Chembath, Anupama; Jefferies, Damien; Basle, Arnaud; Khalid, Syma; Rutherford, Julian C.

    2016-01-01

    Mep2 proteins are fungal transceptors that play an important role as ammonium sensors in fungal development. Mep2 activity is tightly regulated by phosphorylation, but how this is achieved at the molecular level is not clear. Here we report X-ray crystal structures of the Mep2 orthologues from Saccharomyces cerevisiae and Candida albicans and show that under nitrogen-sufficient conditions the transporters are not phosphorylated and present in closed, inactive conformations. Relative to the open bacterial ammonium transporters, non-phosphorylated Mep2 exhibits shifts in cytoplasmic loops and the C-terminal region (CTR) to occlude the cytoplasmic exit of the channel and to interact with His2 of the twin-His motif. The phosphorylation site in the CTR is solvent accessible and located in a negatively charged pocket ∼30 Å away from the channel exit. The crystal structure of phosphorylation-mimicking Mep2 variants from C. albicans show large conformational changes in a conserved and functionally important region of the CTR. The results allow us to propose a model for regulation of eukaryotic ammonium transport by phosphorylation. PMID:27088325

  6. Ionic Liquids with Ammonium Cations as Lubricants or Additives

    SciTech Connect

    Qu, Jun; Blau, Peter Julian; Dai, Sheng; Luo, Huimin; Truhan, Jr., John J

    2006-01-01

    Friction and wear are estimated to cost 6% of the US gross national product, or around $700 billion annually. A new class of more effective lubricants could lead to huge energy savings. Limited recent literature has suggested potential for using room-temperature ionic liquids as lubricants, however only a few out of millions (or more) of species have been evaluated. Recent ORNL work discovered a new category of ionic liquids with ammonium cations that have demonstrated promising lubricating properties as net lubricants or lubricant additives, particularly in lubricating difficult-to-lubricate metals like aluminum. More than 30% friction reduction has been observed on ammonium-based ionic liquids compared to conventional hydrocarbon oils. The inherent polarity of ionic liquids is believed to provide strong adhesion to contact surfaces and form a boundary lubricating film leading to friction and wear reductions. Other advantages of ionic liquids include (1) negligible volatility, (2) high thermal stability, (3) non-flammability, and (4) better intrinsic properties that eliminate the necessity of many expensive lubricant additives. With very flexible molecular structures, this new class of lubricants, particularly ammonium-based ionic liquids, can be tailored to fit a big variety of applications including but not limited to bearings, combustion engines, MEMS, and metal forming.

  7. Effect of ammonium on bacterial adherence to bladder transitional epithelium.

    PubMed

    Parsons, C L; Stauffer, C; Mulholland, S G; Griffith, D P

    1984-08-01

    The virulence of urease-producing bacteria depends on the ability of urease to degrade urea into ammonia and thereby to alkalinize the urine. Infections caused by urease-producing organisms such as Proteus mirabilis are particularly difficult to manage clinically. We have shown that the layer of glycosaminoglycans at the bladder surface protects against infection by blocking the adherence of bacteria to the epithelium. To determine whether urease-producing urinary pathogens owe their virulence in part to an ability to inactivate the protective effect of the glycosaminoglycan layer, we tested the ability of ammonium chloride to alter bacterial adherence to the normal vesical mucosa. We used an in vivo adherence assay that we have described previously in rabbits. Control animals received sodium chloride adjusted to the same pH as the ammonium chloride. We found that 0.25 M ammonium chloride significantly increases bacterial adherence to normal vesical mucosa as compared to adherence in controls receiving 0.25 M sodium chloride (p less than 0.05). These data suggest that urease plays a hitherto undescribed role in bacterial virulence by altering the antiadherence activity of the glycosaminoglycan layer present at the transitional cell surface. PMID:6376829

  8. Preferential uptake of ammonium ions by zinc ferrocyanide

    NASA Technical Reports Server (NTRS)

    Braterman, P. S.; Arrhenius, G.; Hui, S.; Paplawsky, W.; Miller, S. L. (Principal Investigator)

    1995-01-01

    The concentration of ammonia from dilute aqueous solution could have facilitated many prebiotic reactions. This may be especially true if this concentration involves incorporation into an organized medium. We have shown that (unlike iron(III) ferrocyanide) zinc ferrocyanide,Zn2Fe(CN)6 xH2O, preferentially takes up ammonium ions from 0.01 M NH4Cl to give the known material Zn3(NH4)2[Fe(CN)6]2 xH2O, even in the presence of 0.01 M KCl. KCl alone gave Zn3K2[Fe(CN)6]2 xH2O. Products were characterized by elemental (CHN) analysis and powder X-ray diffraction (XRD). We attribute the remarkable specificity for the ammonium ion to the open framework of the product, which offers enough space for hydrogen-bonded ammonium ions, and infer that other inorganic materials with internal spaces rich in water may show a similar preference.

  9. Preparation of nanodispersed titania using stabilized ammonium nitrate melts

    SciTech Connect

    Raciulete, Monica; Kachina, Anna; Puzenat, Eric; Afanasiev, Pavel

    2010-10-15

    An expedite one-step approach using simple precursors has been proposed to obtain metallic oxide compounds and exemplified by preparation of highly dispersed TiO{sub 2}. The technique consists in heating to 400-500 {sup o}C of molten ammonium nitrate stabilized with an organic nitrogen-containing compound (urea, melamine, ammonium oxalate) and containing dissolved metal salt precursor (TiOCl{sub 2}). The crystallites of the resulting TiO{sub 2} demonstrated variable size and shape as a function of stabilizer used. Their activity in photocatalytic oxidation of formic acid also depends on the nature of the stabilizer. The catalysts as-prepared showed high photocatalytic performance, superior to that of the Degussa P25 reference. Nitrogen containing stabilizers play a double role of increasing the process safety and modifying the properties of the solid products. - Graphical abstract: Ammonium nitrate melts stabilized by nitrogen-containing organic molecules can be applied for expedite one-step preparation of highly dispersed oxides, as exemplified by synthesis of titania photocatalysts.

  10. Structural basis for Mep2 ammonium transceptor activation by phosphorylation.

    PubMed

    van den Berg, Bert; Chembath, Anupama; Jefferies, Damien; Basle, Arnaud; Khalid, Syma; Rutherford, Julian C

    2016-01-01

    Mep2 proteins are fungal transceptors that play an important role as ammonium sensors in fungal development. Mep2 activity is tightly regulated by phosphorylation, but how this is achieved at the molecular level is not clear. Here we report X-ray crystal structures of the Mep2 orthologues from Saccharomyces cerevisiae and Candida albicans and show that under nitrogen-sufficient conditions the transporters are not phosphorylated and present in closed, inactive conformations. Relative to the open bacterial ammonium transporters, non-phosphorylated Mep2 exhibits shifts in cytoplasmic loops and the C-terminal region (CTR) to occlude the cytoplasmic exit of the channel and to interact with His2 of the twin-His motif. The phosphorylation site in the CTR is solvent accessible and located in a negatively charged pocket ∼30 Å away from the channel exit. The crystal structure of phosphorylation-mimicking Mep2 variants from C. albicans show large conformational changes in a conserved and functionally important region of the CTR. The results allow us to propose a model for regulation of eukaryotic ammonium transport by phosphorylation. PMID:27088325

  11. Hyperspectral remote sensing in mineral exploration: Ammonium-illite as a pathfinder for gold

    NASA Astrophysics Data System (ADS)

    Browning, David A.

    The presence of ammonium-illite on the Earth's surface has been correlated to known deposits via structures at Carlin-type gold deposits, suggesting its importance as a vector for gold ore. Additionally, ammonium-illite has often been proposed as a geochemical exploration tool due to its formation in hydrothermal systems. Very little work has focused on ammonium-illite as an exploration tool due to the costly, time-consuming, and often inaccurate methods of ammonium detection, such as wet chemical methods or X-Ray Diffraction. Short-wave infrared reflectance spectroscopy has the ability to detect even trace amounts of ammonium quickly and effectively. Two hyperspectral surveys were performed in Elko County, Nevada, USA. The hyperspectral images were processed to identify several clay anomalies, including ammonium-illite, on a regional exploration scale, while field trothing of an existing claim block showed a spatial relationship between ammonium-illite and gold soil anomalies.

  12. Concurrence of Anaerobic Ammonium Oxidation and Organotrophic Denitrification in Presence of p-Cresol.

    PubMed

    González-Blanco, G; Cervantes, F J; Beristain-Cardoso, R; Gómez, J

    2015-08-01

    This study was carried out to evaluate the capacity of anaerobic granular sludge for oxidizing ammonium and p-cresol with nitrate as terminal electron acceptor. Kinetics for the anaerobic oxidation of ammonium and p-cresol is described in this paper. The phenolic compound was very efficiently consumed, achieving 65 % of mineralization. Ammonium and nitrate were also consumed at 83 and 92 %, respectively, being the main product N2. Anaerobic ammonium oxidation was promoted owing to accumulation of nitrite, and it allowed the synergy of anaerobic ammonium oxidation and organotrophic denitrification for the simultaneous removal of ammonium, nitrate, and p-cresol. A carbonaceous intermediate partially identified was transiently accumulated, and it transitorily truncated the respiratory process of denitrification. These experimental results might be considered for defining strategies in order to remove nitrate, ammonium, and phenolic compounds from wastewaters. PMID:26062920

  13. EFFECTS OF AMMONIUM AND NITRATE ON NUTRIENT UPTAKE AND ACTIVITY OF NITROGEN ASSIMILATING ENZYMES IN WESTERN HEMLOCK

    EPA Science Inventory

    Western hemlock seedlings were grown in nutrient solutions with ammonium, nitrate or ammonium plus nitrate as nitrogen sources. he objectives were to examine (1) possible selectivity for ammonium or nitrate as an N source, (2) the maintenance of charge balance during ammonium and...

  14. Glycosylation-related genes in NS0 cells are insensitive to moderately elevated ammonium concentrations

    PubMed Central

    Brodsky, Arthur Nathan; Caldwell, Mary; Bae, Sooneon; Harcum, Sarah W.

    2014-01-01

    NS0 and Chinese hamster ovary (CHO) cell lines are used to produce recombinant proteins for human therapeutics; however, ammonium accumulation can negatively impact cell growth, recombinant protein production, and protein glycosylation. To improve product quality and decrease costs, the relationship between ammonium and protein glycosylation needs to be elucidated. While ammonium has been shown to adversely affect glycosylation-related gene expression in CHO cells, NS0 studies have not been performed. Therefore, this study sought to determine if glycosylation in NS0 cells were ammonium-sensitive at the gene expression level. Using a DNA microarray that contained mouse glycosylation-related and housekeeping genes, the of these genes was analysed in response to various culture conditions – elevated ammonium, elevated salt, and elevated ammonium with proline. Surprisingly, no significant differences in gene expression levels were observed between the control and these conditions. Further, the elevated ammonium cultures were analysed using real-time quantitative reverse transcriptase PCR (qRT-PCR) for key glycosylation genes, and the qRT-PCR results corroborated the DNA microarray results, demonstrating that NS0 cells are ammonium-insensitive at the gene expression level. Since NS0 are known to have elevated nucleotide sugar pools under ammonium stress, and none of the genes directly responsible for these metabolic pools were changed, consequently cellular control at the translational or substrate-level must be responsible for the universally observed decreased glycosylation quality under elevated ammonium. PMID:25062658

  15. Influence of heterogeneous ammonium availability on bacterial community structure and the expression of nitrogen fixation and ammonium transporter genes during in situ bioremediation of uranium-contaminated groundwater

    SciTech Connect

    Mouser, P.J.; N'Guessan, A.L.; Elifantz, H.; Holmes, D.E.; Williams, K.H.; Wilkins, M.J.; Long, P.E.; Lovley, D.R.

    2009-04-01

    The impact of ammonium availability on microbial community structure and the physiological status and activity of Geobacter species during in situ bioremediation of uranium-contaminated groundwater was evaluated. Ammonium concentrations varied by as much as two orders of magnitude (<4 to 400 {micro}M) across the study site. Analysis of 16S rRNA gene sequences suggested that ammonium influenced the composition of the microbial community prior to acetate addition with Rhodoferax species predominating over Geobacter species at the site with the highest ammonium, and Dechloromonas species dominating at sites with lowest ammonium. However, once acetate was added, and dissimilatory metal reduction was stimulated, Geobacter species became the predominant organisms at all locations. Rates of U(VI) reduction appeared to be more related to the concentration of acetate that was delivered to each location rather than the amount of ammonium available in the groundwater. In situ mRNA transcript abundance of the nitrogen fixation gene, nifD, and the ammonium importer gene, amtB, in Geobacter species indicated that ammonium was the primary source of nitrogen during in situ uranium reduction, and that the abundance of amtB transcripts was inversely correlated to ammonium levels across all sites examined. These results suggest that nifD and amtB expression by subsurface Geobacter species are closely regulated in response to ammonium availability to ensure an adequate supply of nitrogen while conserving cell resources. Thus, quantifying nifD and amtB expression appears to be a useful approach for monitoring the nitrogen-related physiological status of Geobacter species in subsurface environments during bioremediation. This study also emphasizes the need for more detailed analysis of geochemical/physiological interactions at the field scale, in order to adequately model subsurface microbial processes.

  16. Inelastic neutron scattering studies of phonon spectra, and simulations of pressure-induced amorphization in tungstates A W O4 (A =Ba ,Sr ,Ca , and Pb )

    NASA Astrophysics Data System (ADS)

    Goel, Prabhatasree; Gupta, M. K.; Mittal, R.; Rols, S.; Achary, S. N.; Tyagi, A. K.; Chaplot, S. L.

    2015-03-01

    Lattice dynamics and high-pressure phase transitions in A W O4 (A =Ba ,Sr ,Ca , and Pb ) have been investigated using inelastic neutron scattering experiments, ab initio density functional theory calculations, and extensive molecular dynamics simulations. The vibrational modes that are internal to W O4 tetrahedra occur at the highest energies consistent with the relative stability of W O4 tetrahedra. The neutron data and the ab initio calculations are found to be in excellent agreement. The neutron and structural data are used to develop and validate an interatomic potential model. The model is used for classical molecular dynamics simulations to study their response to high pressure. We have calculated the enthalpies of the scheelite and fergusonite phases as a function of pressure, which confirms that the scheelite to fergusonite transition is second order in nature. With increase in pressure, there is a gradual change in the A O8 polyhedra, while there is no apparent change in the W O4 tetrahedra. We found that all the four tungstates amorphize at high pressure. This is in good agreement with available experimental observations which show amorphization at around 45 GPa in BaW O4 and 40 GPa in CaW O4 . Further molecular dynamics simulations at high pressure and high temperature indicate that application of pressure at higher temperature hastens the process of amorphization. On amorphization, there is an abrupt increase in the coordination of the W atom while the bisdisphenoids around the A atom are considerably distorted. The pair-correlation functions of the various atom pairs corroborate these observations. Our observations aid in predicting the pressure of amorphization in SrW O4 and PbW O4 .

  17. Ammonium Ion Requirement for the Cell Cycle of Mycobacterium avium

    PubMed Central

    McCarthy, Charlotte

    1978-01-01

    Mycobacterium avium has a defined cell cycle in which small cells elongate to about five times their original length and then divide by fragmentation. The nitrogen requirement for production of maximal number of colony-forming units was assessed by varying concentrations and kinds of nitrogen source in the medium. Ferric ammonium citrate at a concentration in 7H10 medium of 0.17 μmol/ml or ammonium chloride at 0.25 μmol/ml as the nitrogen source permitted the cells to elongate and to undergo limited division, with the final culture at 4 × 107 colony-forming units per ml. Ammonium chloride at 2.5 μmol/ml or glutamine at 1.37 μmol/ml supported completion of the cell cycle with final colony-forming units at about 5 × 108/ml. Other amino acids, including glutamic acid, at 2.5 μmol/ml did not support completion of the cell cycle, although in most cases an intermediate number of colony-forming units per milliliter were formed. Limited uptake of [14C]glutamic acid and uptake of [14C]glutamine were not detectable until cell fission began. Cells not limited for nitrogen took up five times as much 35S during fission as limited cells did during the same time. The nonlimited cells contained 10 times as much sulfolipid as the nitrogen-limited cells at the end of the cell cycle. These results demonstrate that rapidly dividing cells of M. avium utilize amino acids and sulfur and also synthesize sulfolipids in events that are apparently separable from metabolic functions of elongating cells. The results are contrasted with those found for other mycobacteria in which no cell cycle has been demonstrated. Images PMID:624592

  18. Stability of ammonium fluoride-treated Si(100)

    NASA Astrophysics Data System (ADS)

    Houston, Michael R.; Maboudian, Roya

    1995-09-01

    X-ray photoelectron spectroscopy (XPS) and contact angle analyses have been employed to investigate the chemical stability of silicon surfaces treated by an ammonium fluoride (NH4F) solution. Consistent with earlier results [Dumas and Chabal, Chem. Phys. Lett. 181, 537 (1991)], it is found that an NH4F final etch produces surfaces exhibiting lower oxygen and carbon contamination levels in comparison to the surfaces obtained with the traditional HF or buffered HF (BHF) etch. In conjunction with lower contamination levels, surfaces treated in ammonium fluoride show higher contact angles with water, indicating lower surface free energies. The Si-H surfaces produced by the ammonium fluoride etch were found to remain hydrophobic for weeks in air and showed no signs of oxidation for several days. After an induction period of about one week in air, oxidation began to occur in a more rapid fashion. The stability of the Si-H surfaces in water was also investigated, and it was found that the oxygen contamination levels measured by x-ray photoelectron spectroscopy were extremely sensitive to the final rinse time. An induction period of approximately one hour in water existed before any signs of oxidation were evident. Despite the fact that the NH4F-treated samples were initially cleaner than the HF-treated samples, both of these surfaces showed similar temporal behavior in air and water. We attribute this finding to the surface topographies produced by these treatments, as well as to the extreme sensitivity of the results to such factors as water rinse time.

  19. Ammonium Uptake by Phytoplankton Regulates Nitrification in the Sunlit Ocean

    PubMed Central

    Smith, Jason M.; Chavez, Francisco P.; Francis, Christopher A.

    2014-01-01

    Nitrification, the microbial oxidation of ammonium to nitrate, is a central part of the nitrogen cycle. In the ocean’s surface layer, the process alters the distribution of inorganic nitrogen species available to phytoplankton and produces nitrous oxide. A widely held idea among oceanographers is that nitrification is inhibited by light in the ocean. However, recent evidence that the primary organisms involved in nitrification, the ammonia-oxidizing archaea (AOA), are present and active throughout the surface ocean has challenged this idea. Here we show, through field experiments coupling molecular genetic and biogeochemical approaches, that competition for ammonium with phytoplankton is the strongest regulator of nitrification in the photic zone. During multiday experiments at high irradiance a single ecotype of AOA remained active in the presence of rapidly growing phytoplankton. Over the course of this three day experiment, variability in the intensity of competition with phytoplankton caused nitrification rates to decline from those typical of the lower photic zone (60 nmol L−1 d−1) to those in well-lit layers (<1 nmol L−1 d−1). During another set of experiments, nitrification rates exhibited a diel periodicity throughout much of the photic zone, with the highest rates occurring at night when competition with phytoplankton is lowest. Together, the results of our experiments indicate that nitrification rates in the photic zone are more strongly regulated by competition with phytoplankton for ammonium than they are by light itself. This finding advances our ability to model the impact of nitrification on estimates of new primary production, and emphasizes the need to more strongly consider the effects of organismal interactions on nutrient standing stocks and biogeochemical cycling in the surface of the ocean. PMID:25251022

  20. Ammonium uptake by phytoplankton regulates nitrification in the sunlit ocean.

    PubMed

    Smith, Jason M; Chavez, Francisco P; Francis, Christopher A

    2014-01-01

    Nitrification, the microbial oxidation of ammonium to nitrate, is a central part of the nitrogen cycle. In the ocean's surface layer, the process alters the distribution of inorganic nitrogen species available to phytoplankton and produces nitrous oxide. A widely held idea among oceanographers is that nitrification is inhibited by light in the ocean. However, recent evidence that the primary organisms involved in nitrification, the ammonia-oxidizing archaea (AOA), are present and active throughout the surface ocean has challenged this idea. Here we show, through field experiments coupling molecular genetic and biogeochemical approaches, that competition for ammonium with phytoplankton is the strongest regulator of nitrification in the photic zone. During multiday experiments at high irradiance a single ecotype of AOA remained active in the presence of rapidly growing phytoplankton. Over the course of this three day experiment, variability in the intensity of competition with phytoplankton caused nitrification rates to decline from those typical of the lower photic zone (60 nmol L-1 d-1) to those in well-lit layers (<1 nmol L-1 d-1). During another set of experiments, nitrification rates exhibited a diel periodicity throughout much of the photic zone, with the highest rates occurring at night when competition with phytoplankton is lowest. Together, the results of our experiments indicate that nitrification rates in the photic zone are more strongly regulated by competition with phytoplankton for ammonium than they are by light itself. This finding advances our ability to model the impact of nitrification on estimates of new primary production, and emphasizes the need to more strongly consider the effects of organismal interactions on nutrient standing stocks and biogeochemical cycling in the surface of the ocean. PMID:25251022

  1. Study of calcinations of ammonium diuranate at different temperatures

    NASA Astrophysics Data System (ADS)

    Manna, Subhankar; Karthik, Phani; Mukherjee, Abhishek; Banerjee, Joydipta; Roy, Saswati B.; Joshi, Jyeshtharaj B.

    2012-07-01

    Effect of calcination temperature has been studied on tap density, surface area, porosity, O/U ratio, morphology and crystal phases of uranium oxides. The oxides were produced by calcination of ammonium diuranate (ADU). It has been observed that O/U ratio reduces with an increase in temperature. Surface area and porosity increases with temperature, passes through maxima and then reduces. These observations have been explained using high resolution SEM. The crystal phase analysis has shown that the heating of ADU results in to α-U3O8 via β-UO3.

  2. Liquid-phase catalytic oxidation of CO by ammonium persulfate

    SciTech Connect

    Golodov, V.A.; Abilov, M.T.; Sokol'skii, D.V.

    1984-01-01

    The catalytic oxidation of carbon monoxide in aqueous solutions is investigated. The abilities of ammonium persulfate, palladium hydroxide, and silver oxide to force the oxidation are discussed. The rates for these reactions are displayed graphically. The reaction rates as a function of the concentrations of the above-mentioned reactants are determined. An excess of persulfate is found to oxidize Pd(II) to Pd(IV), and this produces a reduction in the rate of CO oxidation. The oxidation of CO is preceeded in the reaction by the interaction of the persulfate with the metal catalyst.

  3. The Properties of Ammonium Dinitramine (ADN): Part 2: Melt Casting

    NASA Astrophysics Data System (ADS)

    Hahma, A.; Edvinsson, H.; Östmark, H.

    2010-04-01

    A melt casting technique for ammonium dinitramine (ADN) and ADN/aluminum was developed. ADN proved relatively easy to cast, when 1% of magnesium oxide was used as a stabilizer and crystallization kernels. Densities of ADN/MgO 99/1 were 92 to 97% of theoretical mean density (TMD) and those of ADN/Al/MgO 64/35/1 were between 95 and 99% of TMD. Sedimentation of Al in the melt was prevented and the particle wetting was ensured by selecting a suitable particle size for Al. No gelling agents or other additives were used. The casting process and factors influencing it are discussed.

  4. Fish gelatin and ammonium dichromate as photosensitive film

    NASA Astrophysics Data System (ADS)

    Orozco-Muñoz, Rosa Elena; Ortiz-Gutiérrez, Mauricio; Salgado-Verduzco, Marco Antonio; Ibarra-Torres, Juan Carlos; Olivares-Pérez, Arturo; Toxqui-López, Santa; Pérez-Cortés, Mario

    2014-02-01

    In this work we propose a phase material based on fish gelatin from Norland Productsmixed with ammonium dichromate deposited on a glass substrate. The photosensitive film has 110 mm thickness. In this material we record low frequency (264 lines/mm) holographic gratings using a λ=532 nm from an Ar laser and reconstruct the image with λ=594 nm from a He-Ne laser. The diffraction efficiency is approximately15% for the first order. The material no requires developing process and is very easy to make. Experimental results are shown.

  5. Morphology and charge transport in ammonium based polymerized ionic liquids

    NASA Astrophysics Data System (ADS)

    Heres, Maximilian; Minutolo, Joseph; Shamblin, Jacob; Long, Maik; Berdzinski, Stefan; Stremel, Veronika; Sangoro, Joshua

    2015-03-01

    Ionic conduction, structural dynamics and morphology in a series of ammonium based polymerized ionic liquids are investigated using broadband dielectric spectroscopy, temperature-modulated differential scanning calorimetry, and neutron as well as x-ray scattering techniques. The dielectric spectra are dominated on the low frequency regime by electrode polarization while hopping conduction is the underlying mechanism at higher frequencies. At their respective calorimetric glass transition temperatures, a strong correlation between the morphology and ionic conductivity is found. These results are discussed within the recent approaches proposed to explain the decoupling of charge transport from structural dynamics. UT/ORNL Science Alliance.

  6. Dimethyl­ammonium guanidinium naphthalene-1,5-disulfonate

    PubMed Central

    Wei, Bin

    2012-01-01

    The asymmetric unit of the title salt, CH6N3 +·C2H8N+·C10H6O6S2 2−, consists of one dimethyl­ammonium cation, one guanidinium cation, and two half naphthalene-1,5-disulfonate anions, which lie on inversion centers. N—H⋯O hydrogen bonds link the cations and anions into layers parallel to the ab plane. The layers have a sandwich-like structure, with the sulfonate groups and cations forming outer slices and the naphthalene ring systems inside. PMID:22589978

  7. Hydroxide Degradation Pathways for Substituted Benzyltrimethyl Ammonium: A DFT Study

    SciTech Connect

    Long, Hai; Pivovar, Bryan S.

    2014-11-01

    The stability of cations used in the alkaline exchange membranes has been a major challenge. In this paper, degradation energy barriers were investigated by density functional theory for substituted benzyltrimethyl ammonium (BTMA+) cations. Findings show that electron-donating substituent groups at meta-position(s) of the benzyl ring could result in increased degradation barriers. However, after investigating more than thirty substituted BTMA+ cations, the largest improvement in degradation barrier found was only 6.7 kJ/mol. This suggests a modest (8×) improvement in stability for this type of approach may be possible, but for anything greater other approaches will need to be pursued.

  8. Laser-induced breakdown spectroscopic study of ammonium nitrate plasma

    SciTech Connect

    Hanif, M.; Salik, M.; Baig, M. A.

    2013-12-15

    We present the optical emission studies of the ammonium nitrate plasma produced by the fundamental (1064 nm) and second (532 nm) harmonics of a Q-switched Nd: YAG laser. The target material was placed in front of the laser beam in an open atmospheric air. The spectrum reveals numerous transitions of neutral nitrogen. We have studied the spatial behavior of the plasma temperature (T{sub e}) and electron number density (N{sub e}) determined using the Boltzmann plot method and Stark broadened line profiles, respectively. Besides, we have studied the variation of the plasma parameters as a function of the laser irradiance.

  9. Thermal properties of quaternary ammonium and pyridinium compounds

    SciTech Connect

    Aksenova, V.P.; Khar'kov, S.N.; Logovotovskaya, V.D.; Belotserkovets, N.I.; Chegolya, A.S.

    1982-12-10

    In the present work an attempt was made at a comprehensive investigation of the influence of the chemical structure of a whole series of cation-active surfactants on the stability to temperature influences, and the general directions of the irreversible transformations at high temperature were established. As a result of a study of processes of thermal decomposition of quaternary ammonium and syridinium salts, quantitative correlations were established according to the influence of the chemical structure of the salts on the limits of thermal stability. On the basis of a detailed analysis of volatile pyrolysis products, concrete schemes of the conversions in the objects studied were proposed.

  10. Molecular recognition of organic ammonium ions in solution using synthetic receptors

    PubMed Central

    Späth, Andreas

    2010-01-01

    Summary Ammonium ions are ubiquitous in chemistry and molecular biology. Considerable efforts have been undertaken to develop synthetic receptors for their selective molecular recognition. The type of host compounds for organic ammonium ion binding span a wide range from crown ethers to calixarenes to metal complexes. Typical intermolecular interactions are hydrogen bonds, electrostatic and cation–π interactions, hydrophobic interactions or reversible covalent bond formation. In this review we discuss the different classes of synthetic receptors for organic ammonium ion recognition and illustrate the scope and limitations of each class with selected examples from the recent literature. The molecular recognition of ammonium ions in amino acids is included and the enantioselective binding of chiral ammonium ions by synthetic receptors is also covered. In our conclusion we compare the strengths and weaknesses of the different types of ammonium ion receptors which may help to select the best approach for specific applications. PMID:20502608

  11. The contribution of exopolysaccharides induced struvites accumulation to ammonium adsorption in aerobic granular sludge.

    PubMed

    Lin, Y M; Bassin, J P; van Loosdrecht, M C M

    2012-03-15

    Aerobic granular sludge from a lab-scale reactor with simultaneous nitrification/denitrification and enhanced biological phosphorus removal processes exhibited significant amount of ammonium adsorption (1.5 mg NH4+-N/g TSS at an ammonium concentration of 30 mg N/L). Potassium release accompanied ammonium adsorption, indicating an ion exchange process. The existence of potassium magnesium phosphate (K-struvite) as one of potassium sources in the granular sludge was studied by X-ray diffraction analysis (XRD). Artificially prepared K-struvite was indeed shown to adsorb ammonium. Alginate-like exopolysaccharides were isolated and their inducement for struvite formation was investigated as well. Potassium magnesium phosphate proved to be a major factor for ammonium adsorption on the granular sludge. Struvites (potassium/ammonium magnesium phosphate) accumulate in aerobic granular sludge due to inducing of precipitation by alginate-like exopolysaccharides. PMID:22209260

  12. Amines and ammonium compounds. CXCVIII. Reaction of ammonium salts containing a 2-alkynyl group with bromine and iodine

    SciTech Connect

    Gyul'nazaryan, A.K.; Khachatryan, N.G.; Saakyan, T.A.; Kinoyan, F.S.; Panosyan, G.A.; Babayan, A.T.

    1988-08-10

    The reactions of monoammonium, 1,4-and 1,5-bistertiaryammonium, and bisquaternary ammonium salts containing a 2-alkynyl group with bromine and iodine were studied. It was shown that these salts form molecular complexes with iodine and that addition of iodine at the triple bond does not occur. In reaction with bromine in all cases except 1,4-bistrimethylammonio-2-butyne dihalides one molecule of the halogen adds at the triple bond with the formation of salts containing the 2,3-dibromo-2-alkenyl group, which then form a 1:1 complex with bromine.

  13. Ammonium nitrate as an oxidizer in solid composite propellants

    NASA Astrophysics Data System (ADS)

    Manelis, G. B.; Lempert, D. B.

    2009-09-01

    Despite the fact that ammonium nitrate (AN) has the highest hydrogen content and fairly high oxygen balance (compared to other oxidizers), its extremely low formation enthalpy and relatively low density makes it one of the worst power oxidizers in solid composite propellants (SCP). Nevertheless, AN has certain advantages - the combustion of the compositions containing AN is virtually safe, its combustion products are ecologically clean, it is very accessible and cheap, and also very thermostable (far more stable than ammonium dinitramide (ADN)). Besides, its low density stops being a disadvantage if the propellant has to be used in deep space and therefore, must be carried there with other rocket carriers. The low cost of AN may also become a serious advantage in the AN application even in lower stages of multistage space launchers as well as in one-stage space launchers with low mass fraction of the propellant. The main specific features relevant to the creation of AN-based SCPs with the optimal energetic characteristics are discussed. The use of metals and their hydrides and proper fuel-binders as well as the recent successes in phase stabilization of AN are described.

  14. Development of electrochemical denitrification from waste water containing ammonium nitrate

    SciTech Connect

    Sawa, Toshio; Hirose, Yasuo; Ishii, Yoshinori; Takatsudo, Atsushi; Wakasugi, Kazuhico; Hayashi, Hiroshi

    1995-12-31

    The authors developed processes to dentrify waste water containing ammonium nitrate discharged from the nuclear fuel manufacturing works and to recover nitric acid and ammonia. For denitrification they applied the operating method and the conditions of operation to make 0.4mM or less from NH{sub 4}NO{sub 3} waste water of 1.5 M by 3 stages of electrodialysis cells. To recover nitric acid and ammonium water, they separated HNO{sub 3} solution of 6 M and NH{sub 4}OH solution with one unit of electrolysis cell, then absorbed NH{sub 3} gas from NH{sub 4}OH solution with water and applied the condition of operation to recover 8 M NH{sub 4}OH solution. The authors demonstrated that treatment and recovery can be carried out stably with actual waste water with a system through the combination of previously mentioned electrodialysis cells, electrolysis cells and an ammonia gas absorber. At present they are planning a plant where NH{sub 4}NO{sub 3} waste water of 4,500 mol can be treated per day.

  15. Steroidal Ammonium Compounds as New Neuromuscular Blocking Agents.

    PubMed

    Rao, Zhigang; Hu, Hao; Tang, Jiazhi; Liu, Zhiying; Yang, Yue; Qiu, Guofu; Xiao, Yuling; Liu, Peng; Hu, Xianming; Zhou, Xiaoju; Hong, Xuechuan

    2016-05-01

    Neuromuscular blocking agents are widely used as an anesthesia auxiliary in surgery, which induce relaxation of skeletal muscles by blocking signal transmission at the neuromuscular junction. Many neuromuscular blocking agents s were developed over the past decades, but none of them fully meets the needs of the clinic by various reasons. In this study, a series of quaternary ammonium steroidal neuromuscular blocking agents were synthesized and evaluated on isolated mouse phrenic nerve-hemidiaphragms for their bioactivities. The initial separation of mono- and bis-quaternary ammonium compounds turned out to be very challenging on regular silica gel chromatography. Therefore, a facile purification method, in which the silica gel was pretreated with methanolic sodium bromide solution, was finally achieved. Compounds 3g (0.36 μm) and 4g (0.37 μm) exhibited excellent neuromuscular blocking activities, which were about sixfold to sevenfold higher in potency than that of rocuronium (2.50 μm). In addition, other bis-quaternized compounds also showed good potencies close to that of rocuronium. Furthermore, the preliminary structure-activity relationship of this series was also elucidated. Benzyl group was found to be a promising quaternary group in this series. PMID:26684806

  16. Manufacture of ammonium sulfate fertilizer from FGD-gypsum

    SciTech Connect

    Chou, M.I.M.; Bruinius, J.A.; Li, Y.C.

    1995-12-31

    The goal of this study is to assess the technical and economic feasibility of producing marketable products, namely fertilizer-grade ammonium sulfate and calcium carbonate, from gypsum produced as part of lime/limestone flue gas desulfurization (FGD) processes. Millions of tons of FGD-gypsum by-product will be produced in this decade. In this study, a literature review and bench-scale experiments were conducted to obtain process data for the production of marketable products from FGD-gypsum and to help evaluate technical and economic feasibility of the process. FGD-gypsum produced at the Abbott power plant in Champaign, IL was used as a raw material. The scrubber, a Chiyoda Thoroughbred 121 FGD, produced a filter cake product contains 98.36% gypsum (CaSO{sub 4}.2H{sub 2}O), and less than 0.01% calcium sulfate (CaSO{sub 3}). Conversion of FGD-gypsum to ammonium sulfate were tested at temperatures between 60 to 70{degrees}C for a duration of five to six hours. The results of a literature review and preliminary bench-scale experiments are presented in this paper.

  17. Shock Initiation and Equation of State of Ammonium Nitrate

    NASA Astrophysics Data System (ADS)

    Robbins, David; Sheffield, Steve; Dattelbaum, Dana; Chellappa, Raja; Velisavljevic, Nenad

    2013-06-01

    Ammonium nitrate (AN) is a widely used fertilizer and mining explosive commonly found in ammonium nitrate-fuel oil. Neat AN is a non-ideal explosive with measured detonation velocities approaching 4 km/s. Previously, we reported a thermodynamically-complete equation of state for AN based on its maximum density, and showed that near-full density AN did not initiate when subjected to shock input conditions up to 22 GPa. In this work, we extend these initial results, by presenting new Hugoniot data for intermediate density neat AN obtained from gas gun-driven plate impact experiments. AN at densities from 1.8 to 1.5 g/cm3 were impacted into LiF windows using a two-stage light gas gun. Dual VISARs were used to measure the interfacial particle velocity wave profile as a function of time following impact. The new Hugoniot data, in addition to updates to thermodynamic parameters derived from structural analysis and vibrational spectroscopy measurements in high pressure diamond anvil cell experiments, are used to refine the unreacted EOS for AN. Furthermore, shock initiation of neat AN was observed as the initial porosity increased (density decreased). Insights into the relationship(s) between initial density and shock initiation sensitivity are also presented, from evidence of shock initiation in the particle velocity profiles obtained for the lower density AN samples.

  18. Antibody purification: ammonium sulfate fractionation or gel filtration.

    PubMed

    Grodzki, Ana Cristina; Berenstein, Elsa

    2010-01-01

    Antibodies can be purified by a variety of methods based on their unique physical and chemical properties such as size, solubility, charge, hydrophobicity and binding affinity. This chapter focuses on ammonium sulfate precipitation as a convenient first step in antibody purification in that, it allows the concentration of the starting material and the precipitation of the desired protein. The principle of ammonium sulfate precipitation lies in "salting out" proteins from the solution. The proteins are prevented to form hydrogen bonds with water and the salt facilitates their interaction with each other forming aggregates that afterward precipitate out of solution. Gel filtration or size- exclusion chromatography is also discussed in this chapter. Gel filtration is based on the relative size of protein molecules and it is of great value to separate IgMs, exchange buffers and/or desalt solutions. The columns designed to separate the proteins are composed of porous beads and the proteins will flow through the packed column inside and around the beads, depending on its size. PMID:20012814

  19. Thermophysical properties of sulfonium- and ammonium-based ionic liquids

    PubMed Central

    Bhattacharjee, Arijit; Luís, Andreia; Lopes-da-Silva, José A.; Freire, Mara G.; Carvalho, Pedro J.; Coutinho, João A. P.

    2014-01-01

    Experimental data for the density, viscosity, refractive index and surface tension of four sulfonium- and ammonium-based Ionic Liquids (ILs) with the common bis(trifluoromethylsulfonyl)imide anion were measured in the temperature range between 288.15 and 353.15 K and at atmospheric pressure. The ILs considered include butyltrimethylammonium bis(trifluoromethylsulfonyl)imide, [N4111][NTf2], tributylmethylammonium bis(trifluoromethylsulfonyl)imide, [N4441][NTf2], diethylmethylsulfonium bis(trifluoromethylsulfonyl)imide, [S221][NTf2], and triethylsulfonium bis(trifluoromethylsulfonyl)imide, [S222][NTf2]. Based on the gathered results and on data taken from literature, the impact of the cation isomerism and of the size of the aliphatic tails, as well as the effect resulting from the substitution of a nitrogen by a sulfur atom as the cation central atom, on the thermophysical properties of sulfonium- and ammonium-based ILs is here discussed. Remarkably, more symmetric cations present a lower viscosity for the same, and sometimes even for higher, alkyl chain lengths at the cation. Additional derivative properties, such as the isobaric thermal expansion coefficient, the surface thermodynamic properties and the critical temperature for the investigated ILs were also estimated and are presented and discussed. PMID:25516634

  20. Release of Ammonium and Mercury from NOx Controlled Fly Ash

    SciTech Connect

    Schroeder, K.T.; Cardone, C.R.; Kim, A.G

    2007-07-01

    One of the goals of the Department of Energy is to increase the reuse of coal utilization byproducts (CUB) to 50% by 2010. This will require both developing new markets and maintaining traditional ones such as the use of fly ash in concrete. However, the addition of pollution control devices can introduce side-effects that affect the marketability of the CUB. Such can be the case when NOx control is achieved using selective catalytic or non-catalytic reduction (SCR or SNCR). Depending on site-specific details, the ammonia slip can cause elevated levels of NH3 in the fly ash. Disposal of ammoniated fly ash can present environmental concerns related to the amount of ammonia that might be released, the amount of water that might become contaminated, and the extent to which metals might be mobilized by the presence of the ammonia. Ammonia retained in fly ash appears to be present as either an ammonium salt or as a chemisorbed species. Mercury in the leachates correlated to neither the amount of leachable ammonium nor to the total amount of Hg in the ash. The strongest correlation was between the decreases in the amount of Hg leached with increased LOI.

  1. Crystal structure of bis­(allyl­ammonium) oxalate

    PubMed Central

    Dziuk, Błażej; Zarychta, Bartosz; Ejsmont, Krzysztof

    2014-01-01

    The title salt, 2C3H8N+·C2O4 2−, crystallized with six independent allyl­ammonium cations and three independent oxalate dianions in the asymmetric unit. One of the oxalate dianions is nearly planar [dihedral angle between CO2 planes = 1.91 (19)°], while the other two are twisted with angles of 11.3 (3) and 26.09 (13)°. One cation has a synperiplanar (cis) conformation with an N—C—C—C torsion angle of 0.9 (3)°, whereas the five remaining cations are characterized by gauche arrangements, with the N—C—C—C torsion angles ranging from 115.9 (12) to 128.8 (3)°. One of the allyl­ammonium cations is positionally disordered (fixed occupancy ratio = 0.45:0.55). In the crystal, the cations and anions are connected by a number of strong N—H⋯O and N—H⋯(O,O) hydrogen bonds, forming layers parallel to (001), with the vinyl groups protruding into the space between the layers. PMID:25553015

  2. Relations of ammonium minerals at several hydrothermal systems in the western U.S.

    NASA Astrophysics Data System (ADS)

    Krohn, M. Dennis; Kendall, Carol; Evans, John R.; Fries, Terry L.

    1993-08-01

    Ammonium bound to silicate and sulfate minerals has recently been located at several major hydrothermal systems in the western U.S. utilizing newly-discovered near-infrared spectral properties. Knowledge of the origin and mineralogic relations of ammonium minerals at known hydrothermal systems is critical for the proper interpretation of remote sensing data and for testing of possible links to mineralization. Submicroscopic analysis of ammonium minerals from two mercury- and gold-bearing hot-springs deposits at Ivanhoe, Nevada and McLaughlin, California shows that the ammonium feldspar, buddingtonite, occurs as fine-grained euhedral crystals coating larger sulfide and quartz crystals. Ammonium feldspar seems to precipitate relatively late in the crystallization sequence and shows evidence for replacement of NH 4 + by K + or other monovalent cations. Some buddingtonite is observed in close association with mercury, but not with gold. Ammonioalunite is found in a variety of isolated crystal forms at both deposits. Nitrogen isotopic values for ammonium-bearing minerals show a 14‰ range in composition, precluding assignment of a specific provenance to the nitrogen. The correlations of nitrogen isotopic values with depth and ammonium content suggest some loss of nitrogen in the oxidizing supergene environment, possibly as a metastable mineral. The high ammonium content in these hydrothermal systems, the close association to mercury, and the small crystal size of the ammonium-bearing minerals all suggest that ammonium may be transported in a late-stage vapor phase or as an organic volatile. Such a process could lead to the formation of a non-carbonaceous organic aureole above a buried geothermal source. The discovery of a 10-km outcrop of ammonium minerals confirms that significant substitution of ammonium in minerals is possible over an extensive area and that remote sensing is a feasible means to detect such aureoles.

  3. Proteins and protein complexes involved in the biochemical reactions of anaerobic ammonium-oxidizing bacteria.

    PubMed

    de Almeida, Naomi M; Maalcke, Wouter J; Keltjens, Jan T; Jetten, Mike S M; Kartal, Boran

    2011-01-01

    It has been less than two decades since anammox (anaerobic ammonium oxidation) coupled to nitrite reduction has been discovered. Already, this process has been recognized as an important sink for fixed nitrogen in the natural environment and has been implemented as a cost-effective ammonium removal technology. Still, little is known about the molecular mechanism of this remarkable reaction. In this mini review, we present an insight into how ammonium and nitrite are combined to form dinitrogen gas. PMID:21265793

  4. Synchrotron X-Ray Topography Study of Structural Defects and Strain in Epitaxial Structures of Yb- and Tm-Doped Potassium Rare-Earth Double Tungstates and Their Influence on Laser Performance.

    SciTech Connect

    Raghothamachar, B.; Carvajal, J; Pujol, M; Mateos, X; Sole, R; Aguilo, M; Diaz, F; Dudley, M

    2010-01-01

    Monoclinic potassium rare-earth double tungstates [KRE(WO{sub 4}){sub 2}, RE = Y, Lu, Yb; KREW] are well suited as hosts for active lanthanide ion (Ln{sup 3+}) dopants for diode-pumped solid-state lasers, with particular interest in thin-disk laser configurations when they are grown as thin films. Using synchrotron white-beam x-ray topography, we have imaged defects and strain in top-seeded solution-grown (TSSG) bulk substrates of different rare-earth tungstates as well as within Yb{sup 3+}- and Tm{sup 3+}-doped epitaxies for thin-disk laser applications grown on these substrates by liquid-phase epitaxy. Higher structural stress in Yb:KYW/KYW epitaxies compared with Yb:KLuW/KLuW epitaxies is found to lower efficiency in laser operation. The quality of Tm:KLuW/KLuW epitaxial films is sensitive to doping level, film thickness, and growth rate. Inhomogeneous stresses within the layers are dominated by lattice-mismatch effects rather than by crystallographic anisotropy.

  5. Distinct Signaling Pathways and Transcriptome Response Signatures Differentiate Ammonium- and Nitrate-supplied Plants

    PubMed Central

    Patterson, Kurt; Cakmak, Turgay; Cooper, Andrew; Lager, Ida; Rasmusson, Allan G.; Escobar, Matthew A.

    2010-01-01

    Nitrogen is the only macronutrient that is commonly available to plants in both oxidized and reduced forms, mainly nitrate and ammonium. The physiological and molecular effects of nitrate supply have been well studied, but comparatively little is known about ammonium nutrition and its differential effects on cell function and gene expression. We have used a physiologically realistic hydroponic growth system to compare the transcriptomes and redox status of the roots of ammonium- and nitrate-supplied Arabidopsis thaliana plants. While ~60% of nitrogen-regulated genes displayed common responses to both ammonium and nitrate, significant “nitrate-specific” and “ammonium-specific” gene sets were identified. Pathways involved in cytokinin response and reductant generation/distribution were specifically altered by nitrate, while a complex biotic stress response and changes in nodulin gene expression were characteristic of ammonium-supplied plants. Nitrate supply was associated with a rapid decrease in H2O2 production, potentially due to an increased export of reductant from the mitochondrial matrix. The underlying basis of the nitrate- and ammonium-specific patterns of gene expression appears to be different signals elaborated from each nitrogen source, including alterations in extracellular pH that are associated with ammonium uptake, downstream metabolites in the ammonium assimilation pathway, and the presence or absence of the nitrate ion. PMID:20444219

  6. Anammox bacteria disguised as denitrifiers: nitrate reduction to dinitrogen gas via nitrite and ammonium.

    PubMed

    Kartal, Boran; Kuypers, Marcel M M; Lavik, Gaute; Schalk, Jos; Op den Camp, Huub J M; Jetten, Mike S M; Strous, Marc

    2007-03-01

    Anaerobic ammonium-oxidizing (anammox) bacteria oxidize ammonium with nitrite and produce N(2). They reside in many natural ecosystems and contribute significantly to the cycling of marine nitrogen. Anammox bacteria generally live under ammonium limitation, and it was assumed that in nature anammox bacteria depend on other biochemical processes for ammonium. In this study we investigated the possibility of dissimilatory nitrate reduction to ammonium by anammox bacteria. Physically purified Kuenenia stuttgartiensis cells reduced (15)NO(3) (-) to (15)NH(4) (+) via (15)NO(2) (-) as the intermediate. This was followed by the anaerobic oxidation of the produced ammonium and nitrite. The overall end-product of this metabolism of anammox bacteria was (15)N(15)N dinitrogen gas. The nitrate reduction to nitrite proceeds at a rate of 0.3 +/- 0.02 fmol cell(-1) day(-1) (10% of the 'normal' anammox rate). A calcium-dependent cytochrome c protein with a high (305 mumol min(-1) mg protein(-1)) rate of nitrite reduction to ammonium was partially purified. We present evidence that dissimilatory nitrate reduction to ammonium occurs in Benguela upwelling system at the same site where anammox bacteria were previously detected. This indicates that anammox bacteria could be mediating dissimilatory nitrate reduction to ammonium in natural ecosystems. PMID:17298364

  7. Quantitative remote sensing of ammonium minerals, Cedar Mountains, Esmeralda County, Nevada

    NASA Technical Reports Server (NTRS)

    Baugh, William M.; Kruse, Fred A.

    1995-01-01

    Mineral-bound ammonium (NH4+) was discovered by the U.S. Geological Survey in the southern Cedar Mountains of Esmeralda County, Nevada in 1989. At 10 km in length, this site is 100 times larger than any previously known occurrence in volcanic rocks. The ammonium occurs in two hydrothermally altered, crystal-rich rhyolitic tuff units of Oligocene age, and is both structurally and stratigraphically controlled. This research uses Advanced Visible/Infrared Imaging Spectrometer (AVIRIS) data to quantitatively map the mineral-bound ammonium (buddingtonite) concentration in the altered volcanic rocks. Naturally occurring mineral-bound ammonium is fairly rare; however, it has been found to occur in gold-bearing hydrothermal deposits. Because of this association, it is thought that ammonium may be a useful too in exploration for gold and other metal deposits. Mineral-bound ammonium is produced when an ammonium ion (NH4+) replaces the alkali cation site (usually K+) in the crystal structure of silicate minerals such as feldspars, micas and clays. Buddingtonite is an ammonium feldspar. The ammonium originates in buried organic plant matter and is transported to the host rock by hydrothermal fluids. Ammonium alteration does not produce visible changes in the rock, and it is barely detectable with standard x-ray diffraction methods. It is clearly identified, however, by absorption features in short wave-infrared (SWIR) wavelengths (2.0 - 2.5 micrometers). The ammonium absorption features are believed to be caused by N-H vibrational modes and are analogous to hydroxyl (O-H) vibrational modes, only shifted slightly in wavelength. Buddingtonite absorption features in the near- and SWIR lie at 1.56, 2.02 and 2.12 micrometers. The feature at 2.12 micrometer is the strongest of the three and is the only one used in this study. The southern Cedar Mountains are sparsely vegetated and are an ideal site for a remote sensing study.

  8. Single stage biological nitrogen removal by nitritation and anaerobic ammonium oxidation in biofilm systems.

    PubMed

    Helmer, C; Tromm, C; Hippen, A; Rosenwinkel, K H; Seyfried, C F; Kunst, S

    2001-01-01

    In full scale wastewater treatment plants with at times considerable deficits in the nitrogen balances, it could hitherto not be sufficiently explained which reactions are the cause of the nitrogen losses and which micro-organisms participate in the process. The single stage conversion of ammonium into gaseous end-products--which is henceforth referred to as deammonification--occurs particularly frequently in biofilm systems. In the meantime, one has succeeded to establish the deammonification processes in a continuous flow moving-bed pilot plant. In batch tests with the biofilm covered carriers, it was possible for the first time to examine the nitrogen conversion at the intact biofilm. Depending on the dissolved oxygen (DO) concentration, two autotrophic nitrogen converting reactions in the biofilm could be proven: one nitritation process under aerobic conditions and one anaerobic ammonium oxidation. With the anaerobic ammonium oxidation, ammonium as electron donor was converted with nitrite as electron acceptor. The end-product of this reaction was N2. Ammonium and nitrite did react in a stoichiometrical ratio of 1:1.37, a ratio which has in the very same dimension been described for the ANAMMOX-process (1:1.31 +/- 0.06). Via the oxygen concentration in the surrounding medium, it was possible to control the ratio of nitritation and anaerobic ammonium oxidation in the nitrogen conversion of the biofilm. Both processes were evenly balanced at a DO concentration of 0.7 mg/l, so that it was possible to achieve a direct, almost complete elimination of ammonium without addition of nitrite. One part of the provided ammonium did participate in the nitritation, the other in the anaerobic ammonium oxidation. Through the aerobic ammonium oxidation into nitrite within the outer oxygen supplied layers of the biofilm, the reaction partner was produced for the anaerobic ammonium oxidation within the inner layers of the biofilm. PMID:11379106

  9. Kinetics of generation, relaxation, and accumulation of electronic excitations under two-photon interband picosecond absorption in tungstate and molibdate crystals

    SciTech Connect

    Lukanin, V. I.; Karasik, A. Ya.

    2013-08-15

    Under two-photon 523.5 nm interband picosecond laser excitation, we measured the kinetics of induced absorption in PbWO{sub 4}, ZnWO{sub 4}, and PbMoO{sub 4} crystals with 532 to 633 nm continuous probe radiation. We obtained real-time information about the dynamics of the generation, relaxation, and accumulations of electronic excitations over a wide time range (from picoseconds to hundreds of seconds) and the 77-300 K temperature range. For the studied crystals, exponential temperature-independent growth of the induced absorption (IA) with 60 ns rise time reflects the dynamics of the generation of electronic excitation. The kinetics of the IA exponential growth with temperature-dependent 3.5-11 {mu}s time constants reflect the dynamics of energy migration between neighboring tungstate (molibdate) ions to traps for the studied crystals. The multiexponential relaxation absorption kinetics strongly depend on temperature, and the relaxation decay time of induced absorption increased from tens to hundreds of milliseconds to seconds under crystal cooling from 300 to 77 K. We found that the increase in the laser pump repetition rate (0-10 Hz) leads to the accumulation of electronic excitations. Control of the repetition rate and the number of excitations allowed us to change the relaxation time of the induced absorption by more than two orders of magnitude. Due to accumulation of excitations at 77 K, the absorption relaxation time can exceed 100 s for PbWO{sub 4} and PbMoO{sub 4} crystals. In the initially transparent crystals, two-photon interband absorption (2PA) leads to crystals opacity at the 523 and 633 nm wavelengths. (An inverse optical transmission of the crystals exceeds 50-55 at a 50-100 GW/cm{sup 2} pump intensity.) Measured at {approx}1 mW probe radiation of 532 and 633 nm wavelengths, the induced absorption values are comparable with those obtained under two-photon absorption at {approx}5 kW pump power. An optical 2PA shutter for the visible spectral range

  10. The crystal and molecular structure of triethanol-ammonium nitrate

    NASA Astrophysics Data System (ADS)

    Bracuti, A. J.

    1992-12-01

    The liquid propellant used in the 155-mm regenerative liquid propellant gun is XM46. XM46 is a solution of 60 percent hydroxyl ammonium nitrate (HAN), 20 percent triethanolammonium nitrate (TEAN), and 20 percent water. This material exhibits rather unusual liquid properties that have been attributed to its being a 'molten eutectic' of fused salts rather than a normal aqueous solution of two different nitrate salts. A hydrogen-bonded liquid structure for eutectic LP1946 was proposed previously based on the known structures of neat HAN and water and a best-guess estimate of the TEAN structure. To verify this estimate, the molecular structure of neat TEAN was recently determined. This investigation revealed TEAN has very unusual and interesting bifurcated intermolecular and trifurcated intramolecular hydrogen bonding configurations within the crystal. If these hydrogen bonding configurations are retained in aqueous solution, they could be responsible in some part to the observed unusual liquid properties of liquid propellant XM46.

  11. Chemical destruction of HMX-based explosives with ammonium hydroxide

    SciTech Connect

    Skidmore, C.; Dell`Orco, P.; Flesner, R.; Kramer, J.; Spontarelli, T.

    1995-09-01

    A series of experiments at Los Alamos National Laboratory explored the efficacy of ammonium hydroxide solutions in converting HMX (cyclotetramethylene-tetranitramine, or Octogen) and HMX-based explosives to nonenergetic, nonhazardous materials. When 80 g of explosive was converted in a reactor operating at 85 psig pressure at 140 C, the principal gaseous products were nitrous oxide (46% to 51%), nitrogen (22% to 32%), and ammonia (17% to 28%). Formate and hexamethylene-tetramine (hexamine) account for effectively 100% of the carbon-bearing aqueous species. Nitrate, nitrite, and acetate were present in the liquid in trace amounts. The process effectively treated molding powders of the plastic-bonded explosives PBX 9501 (2.5% estane), LX-04 (15% viton), and PBX 9404 (3% nitrocellulose). Results were compared with those achieved using sodium hydroxide solutions at 150 C in a pressurized reactor.

  12. Effect of impurities on crystal growth rate of ammonium pentaborate

    NASA Astrophysics Data System (ADS)

    Şahin, Ö.; Özdemir, M.; Genli, N.

    2004-01-01

    The effect of sodium chloride, borax and boric acid of different concentrations on the growth rate of ammonium pentaborate octahydrate crystals (APBO) was measured and was found to depend on supersaturation in a fluidized bed crystallizer. The presence of impurities in APBO solution increases the growth rate compared with growth from pure solution. It was found that the presence of sodium chloride, borax and boric acid decreases the reaction rate constant kr, while it increases the mass-transfer coefficient, K, of APBO crystals. In pure aqueous solution, the crystal growth rate of APBO is mainly controlled by diffusion. However, both diffusion and integration steps affect the growth rate of APBO crystals in the presence of sodium chloride, borax and boric acid. The mass-transfer coefficient, K, reaction rate constant, kr and reaction order, r were calculated from general mass-transfer equation by using genetic algorithm method making no assumption.

  13. Ammonium stress in Arabidopsis: signaling, genetic loci, and physiological targets.

    PubMed

    Li, Baohai; Li, Guangjie; Kronzucker, Herbert J; Baluška, František; Shi, Weiming

    2014-02-01

    Ammonium (NH4(+)) toxicity is a significant ecological and agricultural issue, and an important phenomenon in cell biology. As a result of increasing soil nitrogen input and atmospheric deposition, plants have to deal with unprecedented NH4(+) stress from sources below and above ground. In this review, we describe recent advances in elucidating the signaling pathways and identifying the main physiological targets and genetic loci involved in the effects of NH4(+) stress in the roots and shoots of Arabidopsis thaliana. We outline new experimental approaches that are being used to study NH4(+) toxicity in Arabidopsis and propose an integrated view of behavior and signaling in response to NH4(+) stress in the Arabidopsis system. PMID:24126103

  14. Jupiter’s Great Red Spot and Ammonium Hydrosulfide

    NASA Astrophysics Data System (ADS)

    Hudson, Reggie L.; Loeffler, Mark J.; Chanover , Nancy J.; Simon, Amy A.

    2014-11-01

    The color and composition of Jupiter’s Great Red Spot (GRS) have been studied for over a century, and numerous explanations have been offered for this feature’s origin and properties. Since ammonium hydrosulfide (NH4SH) is thought to be a component of Jupiter’s clouds, and since sulfur chemistry is a rich source of colors, we have initiated a laboratory research program to study this ionic solid and a complementary program of GRS telescopic observations. Our initial experiments have investigated whether NH4SH or its radiation-chemical products might contribute to the spectrum of the GRS. This DPS presentation will cover some of our new results on the thermal and radiolytic stability of NH4SH, along with new infrared and mass spectral measurements. Support by NASA’s Planetary Atmospheres and Outer Planets Research programs is acknowledged.

  15. Crystal structure of tris-(hydroxyl-ammonium) orthophosphate.

    PubMed

    Leinemann, Malte; Jess, Inke; Boeckmann, Jan; Näther, Christian

    2015-11-01

    The crystal structure of the title salt, ([H3NOH](+))3·[PO4](3-), consists of discrete hydroxyl-ammonium cations and ortho-phos-phate anions. The atoms of the cation occupy general positions, whereas the anion is located on a threefold rotation axis that runs through the phospho-rus atom and one of the phosphate O atoms. In the crystal structure, cations and anions are linked by inter-molecular O-H⋯O and N-H⋯O hydrogen bonds into a three-dimensional network. Altogether, one very strong O-H⋯O, two N-H⋯O hydrogen bonds of medium strength and two weaker bifurcated N-H⋯O inter-actions are observed. PMID:26594525

  16. Giant barocaloric effects at low pressure in ferrielectric ammonium sulphate.

    PubMed

    Lloveras, P; Stern-Taulats, E; Barrio, M; Tamarit, J-Ll; Crossley, S; Li, W; Pomjakushin, V; Planes, A; Mañosa, Ll; Mathur, N D; Moya, X

    2015-01-01

    Caloric effects are currently under intense study due to the prospect of environment-friendly cooling applications. Most of the research is centred on large magnetocaloric effects and large electrocaloric effects, but the former require large magnetic fields that are challenging to generate economically and the latter require large electric fields that can only be applied without breakdown in thin samples. Here we use small changes in hydrostatic pressure to drive giant inverse barocaloric effects near the ferrielectric phase transition in ammonium sulphate. We find barocaloric effects and strengths that exceed those previously observed near magnetostructural phase transitions in magnetic materials. Our findings should therefore inspire the discovery of giant barocaloric effects in a wide range of unexplored ferroelectric materials, ultimately leading to barocaloric cooling devices. PMID:26607989

  17. Giant barocaloric effects at low pressure in ferrielectric ammonium sulphate

    PubMed Central

    Lloveras, P.; Stern-Taulats, E.; Barrio, M.; Tamarit, J.-Ll.; Crossley, S.; Li, W.; Pomjakushin, V.; Planes, A.; Mañosa, Ll.; Mathur, N. D.; Moya, X.

    2015-01-01

    Caloric effects are currently under intense study due to the prospect of environment-friendly cooling applications. Most of the research is centred on large magnetocaloric effects and large electrocaloric effects, but the former require large magnetic fields that are challenging to generate economically and the latter require large electric fields that can only be applied without breakdown in thin samples. Here we use small changes in hydrostatic pressure to drive giant inverse barocaloric effects near the ferrielectric phase transition in ammonium sulphate. We find barocaloric effects and strengths that exceed those previously observed near magnetostructural phase transitions in magnetic materials. Our findings should therefore inspire the discovery of giant barocaloric effects in a wide range of unexplored ferroelectric materials, ultimately leading to barocaloric cooling devices. PMID:26607989

  18. Large electrocaloric effects in single-crystal ammonium sulfate.

    PubMed

    Crossley, S; Li, W; Moya, X; Mathur, N D

    2016-08-13

    Electrocaloric (EC) effects are typically studied near phase transitions in ceramic and polymer materials. Here, we investigate EC effects in an inorganic salt, namely ammonium sulfate (NH4)2SO4, with an order-disorder transition whose onset occurs at 223 K on cooling. For a single crystal thinned to 50 μm, we use a Maxwell relation to find a large isothermal entropy change of 30 J K(-1) kg(-1) in response to a field change of 400 kV cm(-1) The Clausius-Clapeyron equation implies a corresponding adiabatic temperature change of 4.5 K.This article is part of the themed issue 'Taking the temperature of phase transitions in cool materials'. PMID:27402930

  19. Generation, behavior, and toxicity of ammonium sulfite aerosols

    SciTech Connect

    Rothenberg, S.J.; Dahl, A.R.; Barr, E.B.; Wolff, R.K.

    1986-01-01

    Ammonium sulfite aerosols were continuously generated for periods up to 6 h by gas phase reaction of sulfur dioxide, ammonia, and water vapor in nitrogen carrier gas. Concentrations from 1 to 500 mg/m/sup 3/ were obtained. Aerosol leaving the generator was greater than 90% sulfite, but when diluted with air preparatory to animal exposures, the aerosol was rapidly oxidized. Sulfite concentrations in a large exposure chamber with a long residence time were consistently less than 25 percent of the aerosol mass. Sulfite concentrations in a nose-only or head-only inhalation chamber 1 ft downstream from a radial air injection system ranged from 10 to 80 percent sulfite. The latter system, with a short residence time, was used to expose animals to aerosols. Effects of the mixed sulfite/sulfate aerosol on acute mortality of guinea pigs and tracheal mucous clearance of dogs were measured and no effects were observed.

  20. Growth and characterization of ammonium acid phthalate single crystals

    NASA Astrophysics Data System (ADS)

    Arunkumar, A.; Ramasamy, P.

    2013-04-01

    Ammonium acid phthalate (AAP) has been synthesized and single crystals were grown by slow evaporation solution growth technique. The unit cell parameters were confirmed by single crystal X-ray diffraction analysis and it belongs to orthorhombic system with the space group of Pcab. The high resolution X-ray diffraction studies revealed the crystalline perfection of the grown crystal. The various functional groups of AAP were identified by FT-IR and Raman spectral analyses. Thermal stability of the grown crystals was studied by TGA/DTA. The optical properties of the grown crystals were analyzed by UV-Vis-NIR and photoluminescence spectral studies. The mechanical property of the grown crystal was studied by Vickers microhardness measurement. The growth features of AAP were analyzed by chemical etching.

  1. Integrated Data Collection Analysis (IDCA) Program — Ammonium Nitrate

    SciTech Connect

    Sandstrom, Mary M.; Brown, Geoffrey W.; Preston, Daniel N.; Pollard, Colin J.; Warner, Kirstin F.; Sorensen, Daniel N.; Remmers, Daniel L.; Phillips, Jason J.; Shelley, Timothy J.; Reyes, Jose A.; Hsu, Peter C.; Reynolds, John G.

    2013-05-17

    The Integrated Data Collection Analysis (IDCA) program is conducting a proficiency study for Small- Scale Safety and Thermal (SSST) testing of homemade explosives (HMEs). Described here are the results for impact, friction, electrostatic discharge, and differential scanning calorimetry analysis of ammonium nitrate (AN). AN was tested, in most cases, as both received from manufacturer and dried/sieved. The participants found the AN to be: 1) insensitive in Type 12A impact testing (although with a wide range of values), 2) completely insensitive in BAM friction testing, 3) less sensitive than the RDX standard in ABL friction testing, 4) less sensitive than RDX in ABL ESD testing, and 5) less sensitive than RDX and PETN in DSC thermal analyses.

  2. Salting out of proteins using ammonium sulfate precipitation.

    PubMed

    Duong-Ly, Krisna C; Gabelli, Sandra B

    2014-01-01

    Protein solubility is affected by ions. At low ion concentrations (<0.5 M), protein solubility increases along with ionic strength. Ions in the solution shield protein molecules from the charge of other protein molecules in what is known as 'salting-in'. At a very high ionic strength, protein solubility decreases as ionic strength increases in the process known as 'salting-out'. Thus, salting out can be used to separate proteins based on their solubility in the presence of a high concentration of salt. In this protocol, ammonium sulfate will be added incrementally to an E. coli cell lysate to isolate a recombinantly over-expressed protein of 20 kDa containing no cysteine residues or tags. PMID:24674064

  3. Ammonium sulfate fractionation and assay of hormone receptors.

    PubMed

    Chen, Y M; Vaughn, C B

    1989-01-01

    Ammonium sulfate (AS) precipitation by consecutive steps at 10% to 50% saturation has been utilized for fractionation of cytoplasmic estrogen receptor (ER) and progesterone receptor (PgR). The highest percentage of both receptor activities are confined mainly in two fractions at AS saturation from 20% to 30% and 30% to 40%. The total percentages of activity of the cytoplasmic ER and PgR salted out at 50% saturation are 77% and 53%, respectively. Precipitation of hormone-receptor complexes at 50% saturation for assay of ER and PgR can be achieved, but needs improvement for efficient salting out of the receptors. ER and PgR salted out in the AS pellet are much more stable for storage than in the cytosol. PMID:2790540

  4. Structural features of two polymorphs of ammonium uranyl crotonate

    NASA Astrophysics Data System (ADS)

    Savchenkov, A. V.; Peresypkina, E. V.; Pushkin, D. V.; Virovets, A. V.; Serezhkina, L. B.; Serezhkin, V. N.

    2014-09-01

    X-ray crystallography, FTIR spectroscopy and thermal analysis were conducted for crystals of two polymorphs of NH4UO2(C3H5COO)3, which are the first examples of uranyl tricarboxylate complexes with ions of unsaturated aliphatic monocarboxylic acid. The main structural units of both polymorphs are anionic complexes [UO2(C3H5COO)3]-. Uranium atoms adopt hexagonal bipyramidal coordination polyhedron, and crotonate ions realize bidentate cyclic type of coordination. Due to different packing of ammonium ions and [UO2(C3H5COO)3]- complexes triclinic crystals of α-polymorph have layer structure and cubic crystals of β-polymorph have three dimensional structure. Features of three dimensional packing of R+ ions and [UO2L3]- complexes in structures of 25 known R[UO2L3] compounds are discussed.

  5. The Use of Quaternary Ammonium to Combat Dental Caries

    PubMed Central

    Ge, Yang; Wang, Suping; Zhou, Xuedong; Wang, Haohao; Xu, Hockin H. K.; Cheng, Lei

    2015-01-01

    Resin composites and adhesives are increasingly popular in dental restorations, but secondary caries is one of the main reasons for restoration failure. Quaternary ammonium monomers (QAMs) have an anti-microbial effect and are widely used in many fields. Since the concept of the immobilized antibacterial effect was put forward, dental restorations containing QAMs have been studied to reduce secondary caries. Previous studies have been struggling to develop novel anti-caries materials which might have triple benefits: good mechanical properties, antibacterial effects and remineralization potentials. Different kinds of QAMs have been proven to be effective in inhibiting the growth and metabolism of biofilms. Combination of QAMs and other nanoparticles in resin composites and adhesives could enhance their anti-caries capability. Therefore, QAMs are promising to show significant impact on the future of restorative and preventive dentistry. PMID:26635932

  6. Crystal structure of tris­(hydroxyl­ammonium) orthophosphate

    PubMed Central

    Leinemann, Malte; Jess, Inke; Boeckmann, Jan; Näther, Christian

    2015-01-01

    The crystal structure of the title salt, ([H3NOH]+)3·[PO4]3−, consists of discrete hydroxyl­ammonium cations and ortho­phos­phate anions. The atoms of the cation occupy general positions, whereas the anion is located on a threefold rotation axis that runs through the phospho­rus atom and one of the phosphate O atoms. In the crystal structure, cations and anions are linked by inter­molecular O—H⋯O and N—H⋯O hydrogen bonds into a three-dimensional network. Altogether, one very strong O—H⋯O, two N—H⋯O hydrogen bonds of medium strength and two weaker bifurcated N—H⋯O inter­actions are observed. PMID:26594525

  7. Equation of state and temperature measurements for shocked ammonium perchlorate

    NASA Astrophysics Data System (ADS)

    Winey, J. M.; Dreger, Z. A.; Gruzdkov, Y. A.; Jensen, B. J.; Gupta, Y. M.

    2000-04-01

    A thermodynamically consistent equation of state (EOS) was developed for unreacted, single-crystal ammonium perchlorate (AP) for shock compression along the [210] and [001] directions. The specific heat, cv, the pressure-temperature coefficient, (∂P/∂T)v, and the isothermal bulk modulus, BT, were determined from Hugoniot and isothermal compression curves, along with available data at atmospheric pressure. The mechanical response of each orientation of the AP crystal was modeled as an isotropic elastic-plastic solid. Above the HEL, the rate dependent yielding of AP was described with a simple overstress model. Time-resolved Raman spectroscopy experiments were carried out to obtain temperatures in the shocked state. These temperature measurements were used to constrain the values of various EOS parameters.

  8. Crystallization kinetics of ammonium perchlorate in MSMPR crystallizer

    NASA Astrophysics Data System (ADS)

    Tanrıkulu, S. Ü.; Eroğlu, İ.; Bulutcu, A. N.; Özkar, S.

    2000-01-01

    The effects of supersaturation level, sodium chloride (NaCl) as impurity, and the suspension density of the crystallizer content on the crystallization kinetics of ammonium perchlorate (AP) were studied in a mixed-suspension mixed-product removal crystallizer. The product crystals have a plate-like morphology. The crystal size distribution is not affected by the supersaturation level. There was a deviation from the ideal population density where the growth rate of pure AP crystallization was size dependent with the order of 0.4 according to Abegg, Stevens and Larson (ASL) model. However, the ASL model was not found to be suitable to express the growth rate of the crystals in NaCl containing AP solution. Also when suspension density of the crystallizer increased, secondary nucleation was observed.

  9. Cross relaxation of the proton magnetization in ammonium compounds

    NASA Astrophysics Data System (ADS)

    Punkkinen, M.; Vuorimäki, A. H.; Ylinen, E. E.

    1990-01-01

    Expressions are derived for the time constants T1D and TSD of the NH 4 protons in tunneling ammonium compounds below the line-width transition temperature. T1D characterizes the speed of the spin-lattice relaxation of the dipolar energy and TSD the speed of the cross relaxation between the A and T symmetry species. The expressions should be valid if all the tunnel splittings between the T species levels are larger than the magnetic dipolar interaction. Predictions are compared with new experimental results on TSD in (NH 4) 2PbCl 6 and with some earlier results on TSD and T1D in (NH 4) 2 SnBr 6 and NH 4ClO 4. They support the conclusion that for T1D> TSD the T levels are nondegenerate, while the condition T1D< TSD refers to at least a partial degeneracy.

  10. Computational Modeling of Degradation of Substituted Benzyltrimethyl Ammonium: Preprint

    SciTech Connect

    Long, H.; Pivovar, B. S.

    2014-09-01

    The degradation of cations on the alkaline exchange membranes is the major challenge for alkaline membrane fuel cells. In this paper, we investigated the degradation barriers by density functional theory for substituted benzyltrimethyl ammonium (BTMA+) cations, which is one of the most commonly used cations for alkaline exchange membranes. We found that substituted cations with electron-releasing substituent groups at meta-position of the benzyl ring could result in improved degradation barriers. However, after investigating more than thirty substituted BTMA+ cations with ten different substituent groups, the largest improvement of degradation barriers is only 1.6 kcal/mol. This implies that the lifetime of alkaline membrane fuel cells could increase from a few months to a few years by using substituted BTMA+ cations, an encouraging but still limited improvement for real-world applications.

  11. Giant barocaloric effects at low pressure in ferrielectric ammonium sulphate

    NASA Astrophysics Data System (ADS)

    Lloveras, P.; Stern-Taulats, E.; Barrio, M.; Tamarit, J.-Ll.; Crossley, S.; Li, W.; Pomjakushin, V.; Planes, A.; Mañosa, Ll.; Mathur, N. D.; Moya, X.

    2015-11-01

    Caloric effects are currently under intense study due to the prospect of environment-friendly cooling applications. Most of the research is centred on large magnetocaloric effects and large electrocaloric effects, but the former require large magnetic fields that are challenging to generate economically and the latter require large electric fields that can only be applied without breakdown in thin samples. Here we use small changes in hydrostatic pressure to drive giant inverse barocaloric effects near the ferrielectric phase transition in ammonium sulphate. We find barocaloric effects and strengths that exceed those previously observed near magnetostructural phase transitions in magnetic materials. Our findings should therefore inspire the discovery of giant barocaloric effects in a wide range of unexplored ferroelectric materials, ultimately leading to barocaloric cooling devices.

  12. Thermophysical properties of two ammonium-based protic ionic liquids

    PubMed Central

    Bhattacharjee, Arijit; Coutinho, João A. P.; Freire, Mara G.; Carvalho, Pedro J.

    2015-01-01

    Experimental data for density, viscosity, refractive index and surface tension are reported, for the first time, in the temperature range between 288.15 K and 353.15 K and at atmospheric pressure for two protic ionic liquids, namely 2-(dimethylamino)-N,N-dimethylethan-1-ammonium acetate, [N11{2(N11)}H][CH3CO2], and N-ethyl-N,N-dimethylammonium phenylacetate, [N112H][C7H7CO2]. The effect of the anion aromaticity and the cation’s aliphatic tails on the studied properties is discussed. From the measured properties temperature dependency the derived properties, such as the isobaric thermal expansion coefficient, the surface entropy and enthalpy, and the critical temperature, were estimated. PMID:26435554

  13. Slow strain rate fracture of high-strength steel at controlled electrochemical potentials in ammonium chloride, potassium chloride, and ammonium nitrate solutions

    SciTech Connect

    Nguyen, D.T.; Nichols, D.E. ); Daniels, R.D. . School of Chemical Engineering and Materials Science)

    1992-08-15

    Slow strain rate testing has been undertaken to determine the effects of individual chemical species on the fracture process of high-strength 4340 steel. Test environments included potassium chloride, ammonium nitrate, and ammonium chloride at concentrations from 0.001 to 1.0 mole por liter at ambient temperature. Tests were performed at cathodic and anodic controlled potentials, as well as at the open-circuit potential, to delineate the stress corrosion cracking range.

  14. Leaching kinetics of malachite in ammonium carbonate solutions

    NASA Astrophysics Data System (ADS)

    Oudenne, Paul D.; Olson, Ferron A.

    1983-03-01

    Leaching of malachite was conducted with ammonium carbonate as lixiviant and with temperature, lixiviant concentration, and particle size as variables. Two stages of reaction were found. In Stage I, the initial dissolution of malachite proceeds rapidly, but after about 10 pct reaction the rate is reduced by surface blockage due to the presence of a needle-structured intermediate, presumably Cu(OH)2. Subsequently, malachite and the intermediate dissolve concurrently. In Stage II, after 90 pct reaction, essentially all of the malachite has dissolved and only the intermediate remains. It dissolves in Stage II. The activation energy is 64 kJ/mole (15.3 kcal/mole) for Stage I and 75 kJ/mole (18 kcal/mole) for Stage II. The rate of reaction in Stage I is proportional to the reciprocal of particle size and is 0.8 order with respect to the concentration of ammonium carbonate. The structures of leaching residues were studied using a scanning electron microscope. The kinetic data (activation energy and entropy), particle size and concentration dependence, residue morphology, and general leaching behavior evident from microscopic monitoring during leaching were used to develop the geometric equation for leaching in Stage I. The equation, based on a heterogeneous reaction with geometric rate control, is: 1 - (1 - α 1/3 = K01/r0/[(NH4)2C03]0.8 exp(-64,000/RT)t. It was deduced that initial steps in reaction were: (1) release of Cu2+ from malachite; (2) initial complexing with ammonia to form Cu(NH3)2+; and (3) subsequent complexing to produce Cu(NH3){4/2+} which is stable in solution at pH 8.8, the buffered pH of reaction. Stage II appears to be a similar reaction except that the reaction obeys cylindrical geometry instead of spherical geometry as in Stage I.

  15. Tetracalcium phosphate composite containing quaternary ammonium dimethacrylate with antibacterial properties

    PubMed Central

    Cheng, Lei; Weir, Michael D.; Limkangwalmongkol, Penwadee; Hack, Gary D.; Xu, Hockin H. K.; Chen, Qianming; Zhou, Xuedong

    2012-01-01

    Tooth caries is a carbohydrate-modified bacterial infectious disease, and recurrent caries is a frequent reason for restoration failure. The objective of this study was to develop a novel antibacterial composite using tetracalcium phosphate (TTCP) fillers and bis(2-methacryloyloxy-ethyl) dimethyl-ammonium bromide, which is a quaternary ammonium dimethacrylate (QADM). QADM was synthesized using 2-(N,N-dimethylamino)ethyl methacrylate and 2-bromoethyl methacrylate and incorporated into a resin. The resin was filled with 40% TTCP and 30% glass particles. The following QADM mass fractions in the composite were tested: 0%, 6%, 12%, and 18%. Streptococcus mutans biofilms were formed on the composites and the colony-forming units (CFUs), metabolic activity, and lactic acid production were measured. The TTCP-QADM composite had flexural strength and elastic modulus similar to those of two commercial composites (p > 0.1). Increasing the QADM content in TTCP composite greatly decreased the bacteria growth and biofilm matrix production. There were significantly more dead bacteria with increasing QADM content. TTCP composite containing 18% QADM had biofilm CFU, metabolic activity, and acid production about half of those without QADM. Inversely linear relationships were established between QADM mass fraction and S. mutans biofilm CFU, metabolic activity, and acid production, with correlation coefficients R2 ≥ 0.98. In conclusion, TTCP-QADM composites were developed and the effect of QADM mass fraction on the antibacterial properties of the composite was determined for the first time. The novel TTCP-QADM composites possessing a strong antibacterial capability, together with calcium phosphate ion release and good mechanical properties, are promising for dental restorations to reduce biofilm growth and recurrent caries. PMID:22190356

  16. PCDD/Fs' suppression by sulfur-amine/ammonium compounds.

    PubMed

    Fu, Jian-Ying; Li, Xiao-Dong; Chen, Tong; Lin, Xiao-Qing; Buekens, Alfons; Lu, Sheng-Yong; Yan, Jian-Hua; Cen, Ke-Fa

    2015-03-01

    Three distinct -S and -NH2 or NH4(+) containing compounds, including ammonium thiosulfate, aminosulfonic acid and thiourea, were studied as polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) inhibitors. All these three -S and -N containing compounds tested show strong suppression of PCDD/Fs formation, especially for thiourea which has not been studied before. With a (S+N)/Cl molar ratio of only 0.47, thiourea could inhibit 97.3% of PCDD/Fs and even 99.8% of I-TEQ. At an unusually high de novo test temperature (650 °C), the PCDD/Fs' formation was still very low but also the inhibition capacity of thiourea was weak, with an efficiency of 59% for PCDD/Fs when with a (S+N)/Cl molar ratio of 1.40. The results also revealed that the inhibition capability of the combined -S/-NH2 or -S/NH4(+) suppressant was strongly influenced by both the nature of the functional group of nitrogen and the value of the molar ratio (S+N)/Cl. The amine functional group -NH2 tends to be more efficient than ammonium NH4(+) and within a certain range a higher (S+N)/Cl value leads to a higher inhibition efficiency. Moreover, the emission of gases was continuously monitored: the Gasmet results revealed that SO2, HCN and NH3 were the most important decomposition products of thiourea. Thiourea is non-toxic, environment-friendly and can be sprayed into the post-combustion zone in form of powder or aqueous solution. The cost of thiourea at least can be partially compensated by its high inhibition efficiency. Therefore, the application of thiourea in a full-scale incinerator system is promising and encouraging. PMID:25481352

  17. 40 CFR 415.240 - Applicability; description of the ammonium chloride production subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 28 2010-07-01 2010-07-01 true Applicability; description of the ammonium chloride production subcategory. 415.240 Section 415.240 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS INORGANIC CHEMICALS MANUFACTURING POINT SOURCE CATEGORY Ammonium Chloride...

  18. 40 CFR 415.240 - Applicability; description of the ammonium chloride production subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 30 2012-07-01 2012-07-01 false Applicability; description of the ammonium chloride production subcategory. 415.240 Section 415.240 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS INORGANIC CHEMICALS MANUFACTURING POINT SOURCE CATEGORY Ammonium Chloride...

  19. 40 CFR 721.10666 - Quaternary ammonium compounds, bis(fattyalkyl) dimethyl, salts with tannins (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Quaternary ammonium compounds, bis... SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10666 Quaternary ammonium compounds... compounds, bis(fattyalkyl) dimethyl, salts with tannins (PMN P-12-437) is subject to reporting under...

  20. 40 CFR 721.10666 - Quaternary ammonium compounds, bis(fattyalkyl) dimethyl, salts with tannins (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Quaternary ammonium compounds, bis... SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10666 Quaternary ammonium compounds... compounds, bis(fattyalkyl) dimethyl, salts with tannins (PMN P-12-437) is subject to reporting under...

  1. Ammonium-oxidizing bacteria facilitate aerobic degradation of sulfanilic acid in activated sludge.

    PubMed

    Chen, Gang; Ginige, Maneesha P; Kaksonen, Anna H; Cheng, Ka Yu

    2014-01-01

    Sulfanilic acid (SA) is a toxic sulfonated aromatic amine commonly found in anaerobically treated azo dye contaminated effluents. Aerobic acclimatization of SA-degrading mixed microbial culture could lead to co-enrichment of ammonium-oxidizing bacteria (AOB) because of the concomitant release of ammonium from SA oxidation. To what extent the co-enriched AOB would affect SA oxidation at various ammonium concentrations was unclear. Here, a series of batch kinetic experiments were conducted to evaluate the effect of AOB on aerobic SA degradation in an acclimatized activated sludge culture capable of oxidizing SA and ammonium simultaneously. To account for the effect of AOB on SA degradation, allylthiourea was used to inhibit AOB activity in the culture. The results indicated that specific SA degradation rate of the mixed culture was negatively correlated with the initial ammonium concentration (0-93 mM, R²= 0.99). The presence of AOB accelerated SA degradation by reducing the inhibitory effect of ammonium (≥ 10 mM). The Haldane substrate inhibition model was used to correlate substrate concentration (SA and ammonium) and oxygen uptake rate. This study revealed, for the first time, that AOB could facilitate SA degradation at high concentration of ammonium (≥ 10 mM) in an enriched activated sludge culture. PMID:25259503

  2. Solid state NMR of SiO 2 nanotube coated ammonium tartrate crystal

    NASA Astrophysics Data System (ADS)

    Lim, A. R.; Schueneman, G. T.; Novak, B. M.

    1999-04-01

    Ammonium tartrate crystal and SiO 2 nanotube coated ammonium tartrate crystal were studied by 13C CP/MAS NMR, and the structure of two samples were verified using the 13C NMR spectrum. The spin-lattice relaxation times for the carbons in the rotating frame, T1 ρ, have been measured as a function of temperature. All relaxation times of the carbons in the two materials undergo slow motions, i.e. motions on the slow side of the T1 ρ minimum. From these relaxation times, we determine the activation energy for the ammonium tartrate crystal and SiO 2 nanotube coated ammonium tartrate crystal, respectively. The activation energies for the SiO 2 nanotube coated ammonium tartrate crystal were found to be generally higher than those of ammonium tartrate crystal. We think that the higher activation energy for the hydrocarbon in the SiO 2 nanotube coated ammonium tartrate crystal is because of the bonding between the oxygen in the SiO 2 nanotube and the hydroxyl group of the ammonium tartrate crystal.

  3. Effects of salinity induced by ammonium sulfate fertilizer on root and shoot growth of highbush blueberry

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Ammonium sulfate fertilizer is commonly used in highbush blueberry, but due to a high relative salinity, it often causes salt damage, particularly in young plants, when too much of the fertilizer is applied. Three experiments were done to determine the sensitivity of ‘Bluecrop’ blueberry to ammonium...

  4. Effects of salinity induced by ammonium sulfate fertilizer on root and shoot growth of highbush blueberry

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Ammonium sulfate fertilizer is commonly used in highbush blueberry (Vaccinium corymbosum L.), but due to a high salt index, it often causes salt damage, particularly in young plants, when too much of the fertilizer is applied. A study was done to determine the sensitivity of blueberry to ammonium su...

  5. 40 CFR 721.10443 - Ethoxylated alkylphenol sulfate, ammonium salt (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... New Uses for Specific Chemical Substances § 721.10443 Ethoxylated alkylphenol sulfate, ammonium salt... identified generically as ethoxylated alkylphenol sulfate, ammonium salt (PMN P-01-470) is subject to... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Ethoxylated alkylphenol...

  6. 75 FR 56489 - Separation Distances of Ammonium Nitrate and Blasting Agents From Explosives or Blasting Agents...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-09-16

    ... definition of ammonium nitrate fertilizer issued by the Fertilizer Institute'' in its ``Definition and Test Procedures for Ammonium Nitrate Fertilizer.'' The Fertilizer Institute (TFI) ] is a voluntary, non-profit trade association of the fertilizer industry that currently has more than 175 members. See...

  7. 76 FR 23569 - Termination of the Suspension Agreement on Solid Fertilizer Grade Ammonium Nitrate From the...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-04-27

    ... Antidumping Duty Investigation: Solid Fertilizer Grade Ammonium Nitrate from the Russian Federation, 64 FR... Less Than Fair Value: Solid Fertilizer Grade Ammonium Nitrate from the Russian Federation, 65 FR 1139..., Investigation No. 731-TA-856 (Preliminary), 64 FR 50103 (September 15, 1999)). On January 7, 2000,...

  8. 76 FR 39847 - Solid Fertilizer Grade Ammonium Nitrate From the Russian Federation; Final Results of the...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-07

    ...: Solid Fertilizer Grade Ammonium Nitrate From the Russian Federation, 64 FR 45236 (August 19, 1999). On... Fertilizer Grade Ammonium Nitrate From the Russian Federation, 65 FR 42669 (July 11, 2000) (``Final... Results of Review.'' \\1\\ See Initiation of Five-Year (``Sunset'') Review, 76 FR 11202 (March 1,...

  9. 75 FR 55991 - Ammonium Formate; Exemption from the Requirement of a Tolerance

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-09-15

    ... April 21, 2006 (71 FR 20671) (FRL-8067- 3), EPA issued a notice pursuant to section 408 of FFDCA, 21 U.S... from the requirement of a tolerance for residues of ammonium formate (CAS Reg. No. 540-69-2) when used... exemption from the requirement of a tolerance for residues of ammonium formate (CAS Reg. No. 540-69-2)...

  10. 77 FR 21527 - Ammonium Nitrate From Russia: Correction to Notice of Opportunity To Request Administrative Review

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-04-10

    ...; Opportunity To Request Administrative Review, 77 FR 63 (April 2, 2012). This notice serves as a correction to... International Trade Administration Ammonium Nitrate From Russia: Correction to Notice of Opportunity To Request... of the antidumping duty orders and inadvertently omitted Ammonium Nitrate from Russia, POR...

  11. Ammonium Inhibits Chromomethylase 3-Mediated Methylation of the Arabidopsis Nitrate Reductase Gene NIA2

    PubMed Central

    Kim, Joo Yong; Kwon, Ye Jin; Kim, Sung-Il; Kim, Do Youn; Song, Jong Tae; Seo, Hak Soo

    2016-01-01

    Gene methylation is an important mechanism regulating gene expression and genome stability. Our previous work showed that methylation of the nitrate reductase (NR) gene NIA2 was dependent on chromomethylase 3 (CMT3). Here, we show that CMT3-mediated NIA2 methylation is regulated by ammonium in Arabidopsis thaliana. CHG sequences (where H can be A, T, or C) were methylated in NIA2 but not in NIA1, and ammonium [(NH4)2SO4] treatment completely blocked CHG methylation in NIA2. By contrast, ammonium had no effect on CMT3 methylation, indicating that ammonium negatively regulates CMT3-mediated NIA2 methylation without affecting CMT3 methylation. Ammonium upregulated NIA2 mRNA expression, which was consistent with the repression of NIA2 methylation by ammonium. Ammonium treatment also reduced the overall genome methylation level of wild-type Arabidopsis. Moreover, CMT3 bound to specific promoter and intragenic regions of NIA2. These combined results indicate that ammonium inhibits CMT3-mediated methylation of NIA2 and that of other target genes, and CMT3 selectively binds to target DNA sequences for methylation. PMID:26834755

  12. Effects of elevated ammonium on glycosylation gene expression in CHO cells.

    PubMed

    Chen, Peifeng; Harcum, Sarah W

    2006-03-01

    The negative effects of ammonium on recombinant protein productivity and glycosylation have been well documented, but the interaction of ammonium on glycosylation genes has not been completely elucidated. In this study, the effects of elevated ammonium on 12 glycosylation related genes in Chinese hamster ovary cells were evaluated by quantitative real time reverse transcriptase polymerase chain reaction. Numerous cytosol and endoplasmic reticulum (ER) localized genes associated with early glycosylation steps were insensitive to the ammonium condition. The initial expression of uridine diphosphate (UDP)-galactose transporter was higher for the ammonium-treated culture, while the initial expressions of cytosine monophosphate (CMP)-sialic acid transporter, beta(1,4)-galactosyltransferase, and UDP-glucose pyrophosphorylase were higher for the control culture. alpha(2,3)-sialyltransferase was observed to have lower expression level under the elevated ammonium condition compared to the control culture. This study indicates that galactosylation and sialylation inhibition is mainly due to decreased gene expression of galactosyltransferase, sialyltransferase, and CMP-sialic acid transporter and not due to sialidase. These unbalanced initial glycosylation and branching steps can explain the higher molecular heterogeneity under ammonium stress. Moreover, this study indicates that elevated ammonium has limited effects on the glycosylation genes associated with the ER and cytosol compared to the genes associated with the Golgi. PMID:16380282

  13. [Mechanism of ammonium removal in the completely autotrophic nitrogen removal in one reactor process].

    PubMed

    Yang, Guo-hong; Fang, Fang; Guo, Jin-song; Qin, Yu; Wei, Ying

    2009-01-01

    Different synthetic wastewaters were used in the batch tests to analyze the intermediate products and the nitrogen balance, and to study the mechanism of ammonium removal in the completely autotrophic nitrogen removal in one reactor process with the sludge cultured in the SBBR completely autotrophic nitrogen removal system. The results showed that 62% of ammonium was converted to such nitrogen compounds as NO2-, NO3-, NH2 OH, N2H4, NO, NO2, N2O and N2 without addition of organic carbon, and N2 took up 90.07%. The ammonium in the completely autotrophic nitrogen removal in one reactor system was removed in many ways. 4.5% of ammonium was removed in the physical-chemical way. 3.73% of ammonium was converted by the conventional nitrification-denitrification process. The quantity of ammonium removed by the completely autotrophic nitrogen removal in one reactor process was 53.77%, which is the largest, and the completely autotrophic nitrogen removal in one reactor process could be realized in two different metabolic pathways. But the effluent ammonium in the anoxic reactor, where enough NO2 present were present, was equal to the blank system, and no ammonium was converted to such nitrogen compounds as NO2- and N2 by Nitrosomonas eutropha using NO2 as electron acceptor, which maybe caused by lack of the function bacteria. PMID:19353865

  14. Racer (40% ammonium nonanoate) broadcast application for broadleaf weed control in spring-transplanted onions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Racer (40% ammonium nonanoate) is a newly approved herbicide for organically grown food crops. Ammonium nonanoate occurs in nature and is primarily formed from biodegradation of higher fatty acids. Field research was conducted in southeast Oklahoma (Atoka County, Lane, OK) to determine the effect ...

  15. Ab initio molecular dynamic study of solid-state transitions of ammonium nitrate

    NASA Astrophysics Data System (ADS)

    Yu, Hongyu; Duan, Defang; Liu, Hanyu; Yang, Ting; Tian, Fubo; Bao, Kuo; Li, Da; Zhao, Zhonglong; Liu, Bingbing; Cui, Tian

    2016-01-01

    High-pressure polymorphism and phase transitions have wide ranging consequences on the basic properties of ammonium nitrate. However, the phase diagram of ammonium nitrate at high pressure and high temperature is still under debate. This study systematically investigates the phase transitions and structural properties of ammonium nitrate at a pressure range of 5-60 GPa and temperature range of 250-400 K by ab initio molecular dynamics simulations. Two new phases are identified: one corresponds to the experimentally observed phase IV’ and the other is named AN-X. Simultaneously, the lattice strains play a significant role in the formation and stabilization of phase IV’, providing a reasonable explanation for experimental observation of phase IV-IV’ transition which only appears under nonhydrostatic pressure. In addition, 12 O atoms neighboring the NH (N atom in ammonium cation) atom are selected as reference system to clearly display the tanglesome rotation of ammonium cation.

  16. Ab initio molecular dynamic study of solid-state transitions of ammonium nitrate

    PubMed Central

    Yu, Hongyu; Duan, Defang; Liu, Hanyu; Yang, Ting; Tian, Fubo; Bao, Kuo; Li, Da; Zhao, Zhonglong; Liu, Bingbing; Cui, Tian

    2016-01-01

    High-pressure polymorphism and phase transitions have wide ranging consequences on the basic properties of ammonium nitrate. However, the phase diagram of ammonium nitrate at high pressure and high temperature is still under debate. This study systematically investigates the phase transitions and structural properties of ammonium nitrate at a pressure range of 5–60 GPa and temperature range of 250–400 K by ab initio molecular dynamics simulations. Two new phases are identified: one corresponds to the experimentally observed phase IV’ and the other is named AN-X. Simultaneously, the lattice strains play a significant role in the formation and stabilization of phase IV’, providing a reasonable explanation for experimental observation of phase IV-IV’ transition which only appears under nonhydrostatic pressure. In addition, 12 O atoms neighboring the NH (N atom in ammonium cation) atom are selected as reference system to clearly display the tanglesome rotation of ammonium cation. PMID:26754622

  17. Anaerobic ammonium oxidation in traditional municipal wastewater treatment plants with low-strength ammonium loading: Widespread but overlooked.

    PubMed

    Wang, Shanyun; Peng, Yongzhen; Ma, Bin; Wang, Shuying; Zhu, Guibing

    2015-11-01

    Occurrence of anaerobic ammonium oxidation (anammox) in marine and freshwater systems has greatly changed our understanding of global nitrogen (N) cycle and promoted the investigation of the role and ecological features of anammox in anthropogenic ecosystems. This study focused on the spatio-temporal abundance, activity, and biodiversity of anammox bacteria in full-scale municipal wastewater treatment plants (WWTPs) via traditional nitrification/denitrification route with low-strength ammonium loading. The anammox bacteria were detected in all the treatment units at the five WWTPs tested, even in aerobic zones (dissolved oxygen >2 mg L(-1)) with abundance of 10(5)-10(7) hydrazine synthase (hzs) gene copies g(-1). The (15)N-isotope tracing technology revealed that the anammox rates in WWTPs ranged from 0.08 to 0.36 μmol N g(-1) h(-1) in winter and 0.12-1.20 μmol N g(-1) h(-1) in summer with contributions of 2.05-6.86% and 1.71-7.26% to N2 production, respectively. The diversity of anammox bacteria in WWTPs was distributed over only two genera, Brocadia and Kuenenia. Additionally, the exploration of potential interspecies relationships indicated that ammonia oxidation bacteria (AOB) was the major nitrite-substrate producer for anammox during nitrification, while Nitrospira, a nitrite oxidation bacteria (NOB), was the potential major competitor for nitrite. These results suggested the contribution of N-removal by the widespread of anammox has been overlooked in traditional municipal WWTPs, and the ecological habitats of anammox bacteria in anthropogenic ecosystems are much more abundant than previously assumed. PMID:26210031

  18. Interaction between Ammonium Toxicity and Green Tide Development Over Seagrass Meadows: A Laboratory Study

    PubMed Central

    Moreno-Marín, Francisco; Vergara, Juan J.; Pérez-Llorens, J. Lucas; Pedersen, Morten F.; Brun, Fernando G.

    2016-01-01

    Eutrophication affects seagrasses negatively by increasing light attenuation through stimulation of biomass of fast-growing, bloom-forming algae and because high concentrations of ammonium in the water can be toxic to higher plants. We hypothesized nevertheless, that moderate amounts of nitrophilic macroalgae that coexists with seagrasses under eutrophic conditions, can alleviate the harmful effects of eutrophication on seagrasses by reducing ammonium concentrations in the seawater to non-toxic levels because such algae have a very large capacity to take up inorganic nutrients. We studied therefore how combinations of different ammonium concentrations (0, 25 and 50 μM) and different standing stocks of macroalgae (i.e. 0, 1 and 6 layers of Ulva sp.) affected survival, growth and net production of the seagrass Zostera noltei. In the absence of Ulva sp., increasing ammonium concentrations had a negative influence on the performance of Z. noltei. The presence of Ulva sp. without ammonium supply had a similar, but slightly smaller, negative effect on seagrass fitness due to light attenuation. When ammonium enrichment was combined with presence of Ulva sp., Ulva sp. ameliorated some of negative effects caused by high ammonium availability although Ulva sp. lowered the availability of light. Benthic microalgae, which increased in biomass during the experiment, seemed to play a similar role as Ulva sp.–they contributed to remove ammonium from the water, and thus, aided to keep the ammonium concentrations experienced by Z. noltei at relatively non-toxic levels. Our findings show that moderate amounts of drift macroalgae, eventually combined with increasing stocks of benthic microalgae, may aid seagrasses to alleviate toxic effects of ammonium under eutrophic conditions, which highlights the importance of high functional diversity for ecosystem resistance to anthropogenic disturbance. PMID:27035662

  19. Interaction between Ammonium Toxicity and Green Tide Development Over Seagrass Meadows: A Laboratory Study.

    PubMed

    Moreno-Marín, Francisco; Vergara, Juan J; Pérez-Llorens, J Lucas; Pedersen, Morten F; Brun, Fernando G

    2016-01-01

    Eutrophication affects seagrasses negatively by increasing light attenuation through stimulation of biomass of fast-growing, bloom-forming algae and because high concentrations of ammonium in the water can be toxic to higher plants. We hypothesized nevertheless, that moderate amounts of nitrophilic macroalgae that coexists with seagrasses under eutrophic conditions, can alleviate the harmful effects of eutrophication on seagrasses by reducing ammonium concentrations in the seawater to non-toxic levels because such algae have a very large capacity to take up inorganic nutrients. We studied therefore how combinations of different ammonium concentrations (0, 25 and 50 μM) and different standing stocks of macroalgae (i.e. 0, 1 and 6 layers of Ulva sp.) affected survival, growth and net production of the seagrass Zostera noltei. In the absence of Ulva sp., increasing ammonium concentrations had a negative influence on the performance of Z. noltei. The presence of Ulva sp. without ammonium supply had a similar, but slightly smaller, negative effect on seagrass fitness due to light attenuation. When ammonium enrichment was combined with presence of Ulva sp., Ulva sp. ameliorated some of negative effects caused by high ammonium availability although Ulva sp. lowered the availability of light. Benthic microalgae, which increased in biomass during the experiment, seemed to play a similar role as Ulva sp.--they contributed to remove ammonium from the water, and thus, aided to keep the ammonium concentrations experienced by Z. noltei at relatively non-toxic levels. Our findings show that moderate amounts of drift macroalgae, eventually combined with increasing stocks of benthic microalgae, may aid seagrasses to alleviate toxic effects of ammonium under eutrophic conditions, which highlights the importance of high functional diversity for ecosystem resistance to anthropogenic disturbance. PMID:27035662

  20. Environmental Factors Affecting Ammonium Oxidation Under Iron Reducing Conditions

    NASA Astrophysics Data System (ADS)

    Jaffe, P. R.; Huang, S.; Ruiz-Urigüen, M.

    2014-12-01

    Ammonium (NH4+) oxidation coupled to iron (Fe) reduction in the absence of oxygen and nitrate/nitrite (NO3-/NO2-) has been reported by several investigators and referred to as Feammox. Feammox is a biological reaction, where Fe(III) is the electron acceptor, which is reduced to Fe(II), and NH4+ is the electron donor, which is oxidized to NO2-. Through a 180-day anaerobic incubation experiment, and using PCR-DGGE, 454-pyosequecing and qPCR analysis, we have shown that an Acidimicrobiaceae bacterium A6, a previously unreported species in the Acidimicrobiaceae family, might be either responsible or plays a key role in the Feammox process, We have enriched these Feammox bacteria (65.8% in terms of cell numbers) in a membrane reactor, and isolated the pure Acidimicrobiaceae bacterium A6 strain in an autotrophic medium. In samples collected and then incubated from a series of local wetland-, upland-, as well as storm-water detention pond-sediments, Feammox activity was only detected in acidic soil environments that contain Fe oxides. Using primers we developed for this purpose, Acidimicrobiaceae bacterium A6 was detected in all incubations where Feammox was observed. Anaerobic incubations of Feammox enrichment cultures adjusted to different pH, revealed that the optimal pH for Feammox is 4 ~ 5, and the reaction does not proceed when pH > 7. Feammox was still proceeding at pH as low as 2. In Feammox culture amended with different Fe(III) sources, Feammox reaction proceeded only when Fe oxides (ferrihydrite or goethite ) were supplied, whereas samples incubated with ferric chloride or ferric citrate showed no measurable NH4+ oxidation. Furthermore, we have also determined from incubation experiments conducted with a temperature gradient (10 ~ 35℃), that the Feammox process was active when the temperature is above 15℃, and the optimal temperature is 20℃. Incubations of enrichment culture with 79% Feammox bacteria appeared to remove circa 8% more NH4+ at 20ºC than at