WorldWideScience

Sample records for ammonium dihydrogen phosphate

  1. Magnitude and nature of the quadratic electro-optic effect in potassium dihydrogen phosphate and ammonium dihydrogen phosphate crystals

    International Nuclear Information System (INIS)

    Gunning, Mark J.; Raab, Roger E.; Kucharczyk, Wlodimierz

    2001-01-01

    Measurements of the magnitude and the sign of certain quadratic electro-optic coefficients of potassium dihydrogen phosphate (KDP) and ammonium dihydrogen phosphate (ADP) were made with an actively stabilized Michelson interferometer. The results obtained for these coefficients are, in units of 10 -20 m 2 V -2 (as opposed to literature values of order 10 -18 m 2 V -2 ), as follows: (KDP)g xxxx =-3.4±0.5, g yyxx =-0.2±0.4, and g zzxx =-0.7±0.4; (ADP)g xxxx =-7.4±1.0, g yyxx =-1.7±0.9, and g zzxx =-1.4±0.9. The quadratic Faust--Henry coefficient describing the lattice and the electronic contributions to the quadratic electro-optic effect in KDP and ADP is estimated from our results. These show that the nonlinear susceptibility responsible for the quadratic electro-optic effect in these crystals is due mainly to nonlinear interactions of the low-frequency electric field with the crystal lattice. Copyright 2001 Optical Society of America

  2. Transmission spectra study of sulfate substituted potassium dihydrogen phosphate

    KAUST Repository

    LI, LIANG; Zhang, Jianqin; Sun, Xun; Zhang, Qiang; Zhao, Xian; Zhang, Xixiang

    2013-01-01

    Potassium dihydrogen phosphate (KDP) crystals with different amounts of sulfate concentration were grown and the transmittance spectrum was studied. A crystal with high sulfate replacement density exhibits heavy absorption property

  3. Transmission spectra study of sulfate substituted potassium dihydrogen phosphate

    KAUST Repository

    LI, LIANG

    2013-04-18

    Potassium dihydrogen phosphate (KDP) crystals with different amounts of sulfate concentration were grown and the transmittance spectrum was studied. A crystal with high sulfate replacement density exhibits heavy absorption property in the ultraviolet region which confirms and agrees well with former results. © 2013 Astro Ltd.

  4. Effect of processing parameters of rotary ultrasonic machining on surface integrity of potassium dihydrogen phosphate crystals

    Directory of Open Access Journals (Sweden)

    Jianfu Zhang

    2015-09-01

    Full Text Available Potassium dihydrogen phosphate is an important optical crystal. However, high-precision processing of large potassium dihydrogen phosphate crystal workpieces is difficult. In this article, surface roughness and subsurface damage characteristics of a (001 potassium dihydrogen phosphate crystal surface produced by traditional and rotary ultrasonic machining are studied. The influence of process parameters, including spindle speed, feed speed, type and size of sintered diamond wheel, ultrasonic power, and selection of cutting fluid on potassium dihydrogen phosphate crystal surface integrity, was analyzed. The surface integrity, especially the subsurface damage depth, was affected significantly by the ultrasonic power. Metal-sintered diamond tools with high granularity were most suitable for machining potassium dihydrogen phosphate crystal. Cutting fluid played a key role in potassium dihydrogen phosphate crystal machining. A more precise surface can be obtained in machining with a higher spindle speed, lower feed speed, and using kerosene as cutting fluid. Based on the provided optimized process parameters for machining potassium dihydrogen phosphate crystal, a processed surface quality with Ra value of 33 nm and subsurface damage depth value of 6.38 μm was achieved.

  5. Szilard-Chalmers Processes in Ammonium Dihydrogen Phosphate as Studied by Electrophoresis and Electron Spin Resonance Techniques; Processus Szilard-Chalmers dans le Phosphate d'Ammonium Biacide Etudies par ELectro- Phorese et Resonance de Spin Electronique; 0418 0417 0423 0427 0414 ; Procesos Szilard-Chalmers en el Fosfato Monoamonico Estudiados por Electroforesis y Resonancia del Spin Electronico

    Energy Technology Data Exchange (ETDEWEB)

    Fenger, J.; Nielsen, S. O. [Danish AEC Research Establishment, Riso (Denmark)

    1965-04-15

    Little direct information is available on the defects produced in crystalline phosphates by recoiling hot atoms from the P{sup 31} (n, {gamma})P{sup 32} nuclear reaction, although detailed information is available on the state of P{sup 32} after dissolution of the neutron irradiated crystals. In an attempt to characterize and identify these defects by electron spin resonance (ESR) we report the results of a study, using electrophoresis and ESR techniques, of single crystals of ammonium dihydrogen phosphate after neutron irradiation in a thermal column at temperatures between -196 Degree-Sign C and 40 Degree-Sign C. The ESR spectra were recorded with irradiated single crystals of ND{sub 4}D{sub 2}PO{sub 4}. Four line systems were found. Three of these, constituting the outer part of the spectrum, reduce to doublets in certain orientations of the crystal suggesting a hyperfine coupling to P{sup 31}. No evidence for coupling to P{sup 32} was found. The central part of the spectrum could also be produced by pure y-irradiation. One of the systems of lines in the outer part of the spectrum has been traced to hot atom recoils from the process N{sup 14}(n, p)C{sup 14} and assigned to phosphite radicals that are oriented in eight different ways in the crystal lattice. The results of thermal and radiation annealing as studied by electrophoresis techniques are briefly discussed. The most remarkable finding was that ND{sub 4}D{sub 2}PO{sub 4} and NH{sub 4}H{sub 2}PO{sub 4} after neutron irradiation at 4 Degree-Sign C, -78 Degree-Sign C and -196 Degree-Sign C differed in their retentions which at all three temperatures were about 50% larger in ND{sub 4}D{sub 2}PO{sub 4}. (author) [French] On dispose de peu de renseignements directs sur les defauts induits dans les phosphates cristallins par les atomes chauds de recul provenant de la reaction nucleaire {sup 31}P(n, {gamma}){sup 32}P, alors que l'on possede des donnees precises sur l'etat de {sup 32}P apres dissolution d

  6. Developing porous carbon with dihydrogen phosphate groups as sulfur host for high performance lithium sulfur batteries

    Science.gov (United States)

    Cui, Yanhui; Zhang, Qi; Wu, Junwei; Liang, Xiao; Baker, Andrew P.; Qu, Deyang; Zhang, Hui; Zhang, Huayu; Zhang, Xinhe

    2018-02-01

    Carbon matrix (CM) derived from biomass is low cost and easily mass produced, showing great potential as sulfur host for lithium sulfur batteries. In this paper we report on a dihydrogen phosphate modified CM (PCM-650) prepared from luffa sponge (luffa acutangula) by phosphoric acid treatment. The phosphoric acid not only increases the surface area of the PCM-650, but also introduces dihydrogen phosphate onto PCM-650 (2.28 at% P). Sulfur impregnated (63.6 wt%) PCM-650/S, in comparison with samples with less dihydrogen phosphate LPCM-650/S, shows a significant performance improvement. XPS analysis is conducted for sulfur at different stages, including sulfur (undischarged), polysulfides (discharge to 2.1 V) and short chain sulfides (discharge to 1.7 V). The results consistently show chemical shifts for S2p in PCM-650, suggesting an enhanced adsorption effect. Furthermore, density functional theory (DFT) calculations is used to clarify the molecular binding: carbon/sulfur (0.86 eV), carbon/Li2S (0.3 eV), CH3-O-PO3H2/sulfur (1.24 eV), and CH3-O-PO3H2/Li2S (1.81 eV). It shows that dihydrogen phosphate group can significantly enhance the binding with sulfur and sulfide, consistent with XPS results. Consequently a CM functionalised with dihydrogen phosphate shows great potential as the sulfur host in a Li-S battery.

  7. Thermodynamic study of dihydrogen phosphate dimerisation and complexation with novel urea- and thiourea-based receptors.

    Science.gov (United States)

    Bregović, Nikola; Cindro, Nikola; Frkanec, Leo; Užarević, Krunoslav; Tomišić, Vladislav

    2014-11-24

    Complexation of dihydrogen phosphate by novel thiourea and urea receptors in acetonitrile and dimethyl sulfoxide was studied in detail by an integrated approach by using several methods (isothermal titration calorimetry, ESI-MS, and (1)H NMR and UV spectroscopy). Thermodynamic investigations into H2PO4(-) dimerisation, which is a process that has been frequently recognised, but rarely quantitatively described, were carried out as well. The corresponding equilibrium was taken into account in the anion-binding studies, which enabled reliable determination of the complexation thermodynamic quantities. In both solvents the thiourea derivatives exhibited considerably higher binding affinities with respect to those containing the urea moiety. In acetonitrile, 1:1 and 2:1 (anion/receptor) complexes formed, whereas in dimethyl sulfoxide only the significantly less stable complexes of 1:1 stoichiometry were detected. The solvent effects on the thermodynamic parameters of dihydrogen phosphate dimerisation and complexation reactions are discussed. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  8. The effect factors of potassium dihydrogen phosphate crystallization in aqueous solution

    Science.gov (United States)

    Zhou, Cun; Sun, Fei; Liu, Xuzhao

    2017-01-01

    The effects of cooling rate and pH on the potassium dihydrogen phosphate crystallization process were studied by means of batch crystallization process. The experiment shows that with the increase of cooling rate, the metastable zone width increase and the induction period decrease. When the pH is 3.0, the metastable zone width and induction period are both the minimum, while the crystallization rate is the highest. The crystallization products were characterized by scanning election microscope. Potassium Dihydrogen Phosphate (KDP) is a kind of excellent nonlinear optical materials, and belongs to tetragonal system, and ideal shape is aggregate of tetragonal prism and tetragonal dipyramid, the (100) cone is alternating accumulation by double positive ions and double negative ions [1-4]. The crystals of aqueous solution method to grow have large electro-optical nonlinear coefficient and high loser-damaged threshold, and it is the only nonlinear optical crystal could be used in inertial confinement fusion (ICF), KDP crystals are the ideal system to study the native defects of complex oxide insulating material [5-7]. With the development of photovoltaic technology, KDP crystals growth and performance have become a research focus worldwide [8, 9]. The merits of the crystallization process directly affect the quality of KDP products, so the study of the effect of crystallization conditions has an important significance on industrial production. This paper studied the change rule of metastable zone width, induction period, crystallization rate and particle size distribution in crystal process, and discussed the technical condition of KDP crystallization.

  9. Comparable stability of Hoogsteen and Watson-Crick base pairs in ionic liquid choline dihydrogen phosphate.

    Science.gov (United States)

    Tateishi-Karimata, Hisae; Nakano, Miki; Sugimoto, Naoki

    2014-01-08

    The instability of Hoogsteen base pairs relative to Watson-Crick base pairs has limited biological applications of triplex-forming oligonucleotides. Hydrated ionic liquids (ILs) provide favourable environments for a wide range of chemical reactions and are known to impact the stabilities of Watson-Crick base pairs. We found that DNA triplex formation was significantly stabilized in hydrated choline dihydrogen phosphate as compared with an aqueous buffer at neutral pH. Interestingly, the stability of Hoogsteen base pairs was found to be comparable with that of Watson-Crick base pairs in the hydrated IL. Molecular dynamics simulations of a DNA triplex in the presence of choline ions revealed that the DNA triplex was stabilized because of the binding of choline ion around the third strand in the grooves. Our finding will facilitate the development of new DNA materials. Our data also indicate that triplex formation may be stabilized inside cells where choline ions and their derivatives are abundant in vivo.

  10. Comparable Stability of Hoogsteen and Watson–Crick Base Pairs in Ionic Liquid Choline Dihydrogen Phosphate

    Science.gov (United States)

    Tateishi-Karimata, Hisae; Nakano, Miki; Sugimoto, Naoki

    2014-01-01

    The instability of Hoogsteen base pairs relative to Watson–Crick base pairs has limited biological applications of triplex-forming oligonucleotides. Hydrated ionic liquids (ILs) provide favourable environments for a wide range of chemical reactions and are known to impact the stabilities of Watson–Crick base pairs. We found that DNA triplex formation was significantly stabilized in hydrated choline dihydrogen phosphate as compared with an aqueous buffer at neutral pH. Interestingly, the stability of Hoogsteen base pairs was found to be comparable with that of Watson–Crick base pairs in the hydrated IL. Molecular dynamics simulations of a DNA triplex in the presence of choline ions revealed that the DNA triplex was stabilized because of the binding of choline ion around the third strand in the grooves. Our finding will facilitate the development of new DNA materials. Our data also indicate that triplex formation may be stabilized inside cells where choline ions and their derivatives are abundant in vivo. PMID:24399194

  11. Habit control of deuterated potassium dihydrogen phosphate crystal for laser applications

    Science.gov (United States)

    Guzman, L. A.; Suzuki, M.; Fujimoto, Y.; Fujioka, K.

    2016-03-01

    In this study we investigate the habit of partially deuterated potassium dihydrogen phosphate (DKDP) crystals in the presence of Al3+ ions. We have grown single DKDP crystals in (50wt% and 80wt%) partially deuterated solutions and in solutions doped with Al3+ ions (2 ppm) by the point-seed rapid growth technique at controlled supercooling (ΔT=10°C). The growth length of each crystal face was measured and the aspect ratio was calculated. We found that crystals grown in partially deuterated solutions are similar in aspect ratio, while, crystals grown in deuterated solutions doped with Al3+ ions showed a relative change in aspect ratio, the crystal increased in size in the pyramidal direction (vertical axis direction). Crystal characteristics were also analyzed by X-ray diffraction, FTIR and Raman spectroscopy. We have speculated that the relative habit modification is due to a probably adsorption and inclusions of Al3+ ions in the prismatic section of the crystal.

  12. Habit control of deuterated potassium dihydrogen phosphate crystal for laser applications

    International Nuclear Information System (INIS)

    Guzman, L A; Suzuki, M; Fujimoto, Y; Fujioka, K

    2016-01-01

    In this study we investigate the habit of partially deuterated potassium dihydrogen phosphate (DKDP) crystals in the presence of Al 3+ ions. We have grown single DKDP crystals in (50wt% and 80wt%) partially deuterated solutions and in solutions doped with Al 3+ ions (2 ppm) by the point-seed rapid growth technique at controlled supercooling (ΔT=10°C). The growth length of each crystal face was measured and the aspect ratio was calculated. We found that crystals grown in partially deuterated solutions are similar in aspect ratio, while, crystals grown in deuterated solutions doped with Al 3+ ions showed a relative change in aspect ratio, the crystal increased in size in the pyramidal direction (vertical axis direction). Crystal characteristics were also analyzed by X-ray diffraction, FTIR and Raman spectroscopy. We have speculated that the relative habit modification is due to a probably adsorption and inclusions of Al 3+ ions in the prismatic section of the crystal. (paper)

  13. Figuring process of potassium dihydrogen phosphate crystal using ion beam figuring technology.

    Science.gov (United States)

    Li, Furen; Xie, Xuhui; Tie, Guipeng; Hu, Hao; Zhou, Lin

    2017-09-01

    Currently, ion beam figuring (IBF) technology has presented many excellent performances in figuring potassium dihydrogen phosphate (KDP) crystals, such as it is a noncontact figuring process and it does not require polishing fluid. So, it is a very clean figuring process and does not introduce any impurities. However, the ion beam energy deposited on KDP crystal will heat the KDP crystal and may generate cracks on it. So, it is difficult directly using IBF technology to figure KDP crystal, as oblique incident IBF (OI-IBF) has lower heat deposition, higher removal rate, and smoother surface roughness compared to normal incident IBF. This paper studied the process of using OI-IBF to figure KDP crystal. Removal rates and removal functions at different incident angles were first investigated. Then heat depositions on a test work piece were obtained through experiments. To validate the figuring process, a KDP crystal with a size of 200  mm×200  mm×12  mm was figured by OI-IBF. After three iterations using the OI-IBF process, the surface error decreases from the initial values with PV 1.986λ RMS 0.438λ to PV 0.215λ RMS 0.035λ. Experimental results indicate that OI-IBF is feasible and effective to figure KDP crystals.

  14. Large potassium dihydrogen phosphate crystal growth using a three-vessel system for fusion lasers

    International Nuclear Information System (INIS)

    Sasaki, T.; Yokotani, A.; Yamanaka, T.; Nakai, S.; Yamanaka, C.

    1989-01-01

    Large scale laser fusion experiments are being performed in the Institute of Laser Engineering, Osaka University, using the glass laser system Gekko-XII. For this laser, very large nonlinear crystals of potassium dihydrogen phosphate (KDP) with a cross section over 40 X 40 cm is needed as a frequency converter to obtain a short wavelength laser. Generally the temperature falling method (TFM) is used to grow such a huge crystal, but the volume of the growing vessel becomes tremendously large. The three-vessel system (TVS), which is a constant temperature and concentration method, allows better control of supersaturation than does the TFM, and the volume of the main growth vessel can be smaller than that in the case of the TFM. The authors have constructed a TVS. The KDP crystal grew in the growth tank that was kept at a constant temperature of 20 +- 0.01 0 C. The authors show the growth history of the KDP crystal of a 40- X 40-cm cross section. This system is now being operated to obtain the KDP of 100-cm height, and a theoretical estimate of the growth rate is under consideration. These results are presented

  15. Optical and environmentally protective coatings for potassium dihydrogen phosphate (KDP) harmonic converter crystals

    International Nuclear Information System (INIS)

    Thomas, I.M.

    1991-01-01

    Potassium dihydrogen phosphate (KDP) crystals have been used as harmonic converters on the Nova laser at LLNL for over six years. All crystals were coated with a single layer, quarterwave AR coating of porous silica with a refractive index of 1.22. This was prepared by a sol-gel process and was applied from a colloidal suspension by spin coating at room temperature. A few crystals were also coated with a methyl silicone coating prior to the application of the AR coating for environmental protection. The initial optical performance of all crystals was very good but there has been some deterioration over the years because of environmental and laser damage degradation. The deterioration in the silicone samples was, however, much less than the others. We are now in the process of replacing all ten KDP arrays with new crystals and will apply the silicone undercoat to all samples. Recently we have been evaluating a new perfluorinated organic polymer coating which has a refractive index of 1.29. This material is soluble in fluorinated solvents and can be applied by dip coating from solution at room temperature. We hope that this can provide environmental protection when applied to KDP and also act as an AR coating at the same time. The optical performance is not as good as our porous silica because of the higher index; about 0.3% reflection per surface is obtained. 4 refs., 10 figs., 1 tab

  16. Microindentation deformation of lithium dihydrogen phosphate single crystals: Microhardness measurement and indentation size effect

    Energy Technology Data Exchange (ETDEWEB)

    Iurchenko, Anton [Institute for Single Crystals, National Academy of Sciences of Ukraine, Lenin Avenue 60, 61001 Kharkiv (Ukraine); Borc, Jarosław, E-mail: j.borc@pollub.pl [Department of Applied Physics, Lublin University of Technology, ul. Nadbystrzycka 38, 20-618 Lublin (Poland); Sangwal, Keshra [Department of Applied Physics, Lublin University of Technology, ul. Nadbystrzycka 38, 20-618 Lublin (Poland); Voronov, Alexei [Institute for Single Crystals, National Academy of Sciences of Ukraine, Lenin Avenue 60, 61001 Kharkiv (Ukraine)

    2016-02-15

    The Vickers microhardness H{sub V} of the (110) and (111) as-grown faces of lithium dihydrogen phosphate (LDP) crystals was investigated as a function of applied load P. The microhardness H{sub V} of the two faces increases with load P i.e. reverse indentation size effect (reverse ISE) and the hardness of the (110) face is somewhat lower than that of the (111) face but this difference is not easily recognized for these planes due to large scatter in the data. The origin of observed ISE was analyzed using different approaches. It was found that: (1) Hays–Kendall's and Begley–Hutchinson's relations do not explain the origin of reverse ISE but Meyer's law describes the reverse ISE satisfactorily and its constants provide a link between ISE and formation of radial cracks with applied indentation load P, (2) reverse ISE is associated with tensile surface stresses, (3) despite its failure to explain reverse ISE, Begley–Hutchinson's relation is reliable to obtain load-independent hardness H{sub 0}, is 2337 MPa for LDP, and (4) the value of fracture toughness K{sub C} of LDP crystals lies between 4.7 and 12 MPa m{sup 1/2}. The load-independent hardness H{sub 0} of LDP is higher by a factor of 1.5 than that reported for undoped KDP and ADP crystals whereas its fracture toughness K{sub C} is higher by factor of about 20 than that of undoped KDP crystals. - Highlights: • Vickers indentations on the (110) and (111) faces of LDP crystals were made. • The microhardness H{sub V} was investigated as a function of applied load P. • Reverse indentation size effect was observed. • Fracture toughness K{sub C} from the radial cracks was calculated.

  17. Microindentation deformation of lithium dihydrogen phosphate single crystals: Microhardness measurement and indentation size effect

    International Nuclear Information System (INIS)

    Iurchenko, Anton; Borc, Jarosław; Sangwal, Keshra; Voronov, Alexei

    2016-01-01

    The Vickers microhardness H_V of the (110) and (111) as-grown faces of lithium dihydrogen phosphate (LDP) crystals was investigated as a function of applied load P. The microhardness H_V of the two faces increases with load P i.e. reverse indentation size effect (reverse ISE) and the hardness of the (110) face is somewhat lower than that of the (111) face but this difference is not easily recognized for these planes due to large scatter in the data. The origin of observed ISE was analyzed using different approaches. It was found that: (1) Hays–Kendall's and Begley–Hutchinson's relations do not explain the origin of reverse ISE but Meyer's law describes the reverse ISE satisfactorily and its constants provide a link between ISE and formation of radial cracks with applied indentation load P, (2) reverse ISE is associated with tensile surface stresses, (3) despite its failure to explain reverse ISE, Begley–Hutchinson's relation is reliable to obtain load-independent hardness H_0, is 2337 MPa for LDP, and (4) the value of fracture toughness K_C of LDP crystals lies between 4.7 and 12 MPa m"1"/"2. The load-independent hardness H_0 of LDP is higher by a factor of 1.5 than that reported for undoped KDP and ADP crystals whereas its fracture toughness K_C is higher by factor of about 20 than that of undoped KDP crystals. - Highlights: • Vickers indentations on the (110) and (111) faces of LDP crystals were made. • The microhardness H_V was investigated as a function of applied load P. • Reverse indentation size effect was observed. • Fracture toughness K_C from the radial cracks was calculated.

  18. Biocompatibility of the titanium-based implant surfaces: Effect of the calcium dihydrogen phosphate on osteoblast cells

    Directory of Open Access Journals (Sweden)

    Kaluđerović Milena R.

    2016-01-01

    Full Text Available The influence of the presence of calcium dihydrogen phosphate in acid media on titanium-based implant surfaces, Ticer, employed in clinics, and its white form (Ticer white, on osteoblast cells was investigated. Novel surfaces M1 and M2 were obtained by immersing Ticer and Ticer white surfaces in calcium dihydrogen phosphate solution at pH 3.5. The surfaces were characterized by SEM, EDS and X-ray diffraction. The results related to interaction of investigated surfaces and human osteoblast cells from indirect biocompatibility (MTT and SRB assays, proliferation (DAPI assay and mode of cell death (acridine orange/ethidium bromide (AO/EB double staining were found to be in good agreement, as well as findings from osteocalcin (OC and bone sialoprotein (BSP expression. Surfaces were obtained by employing anodic plasma-electrochemical oxidation with spark discharges without subsequent surface modifications were found to be more compatible. Soaking of Ticer and Ticer white in phosphate solution gave toxic materials (M1 and M2 which induced apoptosis and secondary necrosis in osteoblast cells.

  19. The pH behavior of a 2-aminoethyl dihydrogen phosphate zwitterion studied with NMR-titrations

    Science.gov (United States)

    Myller, A. T.; Karhe, J. J.; Haukka, M.; Pakkanen, T. T.

    2013-02-01

    In this study a bifunctional 2-aminoethyl dihydrogen phosphate (AEPH2) was 1H and 31P NMR characterized in a pH range of 1-12 in order to determine the zwitterion properties in different pH regions in H2O and D2O solutions. NMR was also used to determine the pH range where AEPH2 exists as a zwitterion. The phosphate group has two deprotonation points, around pH 1 and 6, while the amino group deprotonates at pH 11. The zwitterion form of AEPH2 (NH3+sbnd CHsbnd CHsbnd OPOH) exists as the main ion between pH 1 and 6 in water solutions and also in the solid state.

  20. Optimalisation of magnesium ammonium phosphate precipitation and its applicability to the removal of ammonium.

    Science.gov (United States)

    Demeestere, K; Smet, E; Van Langenhove, H; Galbacs, Z

    2001-12-01

    Among the physico-chemical abatement technologies, mainly acid scrubbers have been used to control NH3-emission. The disadvantage of this technique is that it yields waste water, highly concentrated in ammonia. In this report, the applicability of the magnesium ammonium phosphate (MAP) process to regenerate the liquid phase, produced by scrubbing NH3-loaded waste gases, was investigated. In the MAP process, ammonium is precipitated as magnesium ammonium phosphate, which can be used as a slow release fertilizer. The influence of a number of parameters, e.g. pH, kinetics, molar ratio NH(+)4/Mg2+/PO(3-)4 on the efficiency of the formation of MAP and on the ammonium removal efficiency was investigated. In this way, optimal conditions were determined for the precipitation reaction. Next to this, interference caused by other precipitation reactions was studied. At aqueous NH(+)4-concentrations of about 600 mg l(-1), ammonium removal efficiencies of 97% could be obtained at a molar ratio NH(+)4/Mg2+/PO(3-)4 of 1/1.5/1.5. To obtain this result, the pH was continuously adjusted to a value of 9 during the reaction. According to this study, it is obvious that the MAP-precipitation technology offers opportunities for ammonium removal from scrubbing liquids. The practical applicability of the MAP-process in waste gas treatment systems, however, should be the subject for further investigations.

  1. Synthesis and crystal structure of 4-fluorobenzylammonium dihydrogen phosphate, [FC6H4CH2NH3]H2PO4

    Directory of Open Access Journals (Sweden)

    Ali Rayes

    2016-12-01

    Full Text Available The asymmetric unit of the title salt, [p-FC6H4CH2NH3]+·H2PO4−, contains one 4-fluorobenzylammonium cation and one dihydrogen phosphate anion. In the crystal, the H2PO4− anions are linked by O—H...O hydrogen bonds to build corrugated layers extending parallel to the ab plane. The FC6H4CH2NH3+ cations lie between these anionic layers to maximize the electrostatic interactions and are linked to the H2PO4− anions through N—H...O hydrogen bonds, forming a three-dimensional supramolecular network. Two hydrogen atoms belonging to the dihydrogen phosphate anion are statistically occupied due to disorder along the OH...HO direction.

  2. Laser Induced Damage of Potassium Dihydrogen Phosphate (KDP Optical Crystal Machined by Water Dissolution Ultra-Precision Polishing Method

    Directory of Open Access Journals (Sweden)

    Yuchuan Chen

    2018-03-01

    Full Text Available Laser induced damage threshold (LIDT is an important optical indicator for nonlinear Potassium Dihydrogen Phosphate (KDP crystal used in high power laser systems. In this study, KDP optical crystals are initially machined with single point diamond turning (SPDT, followed by water dissolution ultra-precision polishing (WDUP and then tested with 355 nm nanosecond pulsed-lasers. Power spectral density (PSD analysis shows that WDUP process eliminates the laser-detrimental spatial frequencies band of micro-waviness on SPDT machined surface and consequently decreases its modulation effect on the laser beams. The laser test results show that LIDT of WDUP machined crystal improves and its stability has a significant increase by 72.1% compared with that of SPDT. Moreover, a subsequent ultrasonic assisted solvent cleaning process is suggested to have a positive effect on the laser performance of machined KDP crystal. Damage crater investigation indicates that the damage morphologies exhibit highly thermal explosion features of melted cores and brittle fractures of periphery material, which can be described with the classic thermal explosion model. The comparison result demonstrates that damage mechanisms for SPDT and WDUP machined crystal are the same and WDUP process reveals the real bulk laser resistance of KDP optical crystal by removing the micro-waviness and subsurface damage on SPDT machined surface. This improvement of WDUP method makes the LIDT more accurate and will be beneficial to the laser performance of KDP crystal.

  3. Synthesis, growth, structure, mechanical and optical properties of a new semi-organic 2-methyl imidazolium dihydrogen phosphate single crystal

    Energy Technology Data Exchange (ETDEWEB)

    Nagapandiselvi, P., E-mail: nagapandiselvip@ssn.edu.in [Department of Physics, SSN College of Engineering, Kalavakkam (India); Baby, C. [Sophisticated Analytical Instrument Facility, Indian Institute of Technology Madras, Chennai (India); Gopalakrishnan, R. [Crystal Research Lab, Department of Physics, Anna University, Chennai (India)

    2016-09-15

    Highlights: • 2MIDP crystals were grown by slow evaporation solution growth technique. • Single crystal XRD revealed self-assembled supramolecular framework. • Z scan technique is employed for third order nonlinear optical susceptibility. • Structure-property correlation is established. - Abstract: A new semi-organic compound, 2-methyl imidazolium dihydrogen phosphate (2MIDP), was prepared and good quality single crystals of 2MIDP were grown by slow evaporation solution growth technique. Crystal structure elucidated using Single crystal XRD showed that 2MIDP crystallizes in monoclinic system with P2{sub 1}/c space group. FT-IR, UV-Vis-NIR, Fluorescence and FT-NMR spectra confirm the molecular structure of 2MIDP. The UV-Vis-NIR spectra established the suitability of the compound for NLO applications. TG-DSC showed that 2MIDP is thermally stable up to 200 °C. Mechanical characteristics like hardness number (H{sub v}), stiffness constant (C{sub 11}), yield strength (σ{sub v}), fracture toughness (K{sub c}) and brittleness index (B{sub i}) were assessed using Vicker’s microhardness tester. Third order nonlinear optical properties determined from Z-scan measurement using femto and picosecond lasers showed two photon reverse saturable absorption. The enhancement of nonlinear optical properties in femto second laser, revealed the suitability of 2MIDP for optical limiting applications.

  4. Effect of L-Cysteine doping on growth and some characteristics of potassium dihydrogen phosphate single crystals

    Science.gov (United States)

    Mahadik, Ashwini; Soni, P. H.; Desai, C. F.

    2017-12-01

    Among quite a number of technologically important NLO materials, Potassium Dihydrogen Phosphate (KDP) is one of the most favourable ones for second harmonic generation applications, such as in electro-optic modulators, parametric oscillators and harmonic generators. The authors report here their studies on KDP crystals doped with L-Cysteine (1 mol% and 2 mol%). The dopant inclusion in the crystals was confirmed using Fourier transform infrared (FT-IR) spectroscopy and Powder X-Ray Diffraction (XRD). The XRD results also confirm the tetragonal structure with lattice parameters a = b = 7.45 Å and c = 6.98 Å. The presence of functional groups of crystals was analyzed using the FTIR spectra. For band gap evaluation, UV-Vis spectra were used and it was found to be 3.41 eV, 4.40eVand 4.50 eV, respectively in the cases of pure KDP, 1 mol% and 2 mol% L-Cysteine dopings. The spectra quality indicates good transparency of the doped crystals in the visible region, a feature quite desirable for applications in optoelectronics.

  5. The impact of dihydrogen phosphate anions on the excited-state proton transfer of harmane. Effect of β-cyclodextrin on these photoreactions.

    Science.gov (United States)

    Reyman, Dolores; Viñas, Montserrat H; Tardajos, Gloria; Mazario, Eva

    2012-01-12

    Photoinduced proton transfer reactions of harmane (1-methyl-9H-pyrido[3,4-b]indole) (HAR) in the presence of a proton donor/acceptor such as dihydrogen phosphate anions in aqueous solution have been studied by stationary and time-resolved fluorescence spectroscopy. The presence of high amounts of dihydrogen phosphate ions modifies the acid/base properties of this alkaloid. Thus, by keeping the pH constant at pH 8.8 and by increasing the amount of NaH(2)PO(4) in the solution, it is possible to reproduce the same spectral profiles as those obtained in high alkaline solutions (pH >12) in the absence of NaH(2)PO(4). Under these conditions, a new fluorescence profile appears at around 520 nm. This result could be related to the results of a recent investigation which suggests that a high intake of phosphates may promote skin tumorigenesis. The presence of β-cyclodextrin (β-CD) avoids the proton transfer reactions in this alkaloid by means the formation of an inclusion complex between β-CD and HAR. The formation of this complex originates a remarkable enhancement of the emission intensity from the neutral form in contrast to the cationic and zwitterionic forms. A new lifetime was obtained at 360 nm (2.5 ns), which was associated with the emission of this inclusion complex. At this wavelength, the fluorescence intensity decay of HAR can be described by a linear combination of two exponentials. From the ratio between the pre-exponential factors, we have obtained a value of K = 501 M for the equilibrium of formation of this complex.

  6. Thermal, Dielectric Studies on Pure and Amino Acid L-Glutamic Acid, L-Histidine L-Valine Doped Potassium Dihydrogen Phosphate Single Crystals

    Science.gov (United States)

    Kumaresan, P.; Babu, S. Moorthy; Anbarasan, P. M.

    Amino acids (L-Glutamic acid, L-Histidine, L-Valine) doped potassium dihydrogen phosphate crystals were grown by the solution growth technique. Slow cooling as well as slow evaporation methods were employed to grow these crystals. The concentration of dopants in the mother solution was varied from 0.1 mole % to 10 mole %. The solubility data for all dopant concentrations were determined. The variation in pH and the corresponding habit modification of the grown crystals were characterized with UV - VIS, FT-IR and SHG trace elements, and dielectric studies reveal slight distortion of lattice parameter for the heavily doped KDP crystals. TGA-DTA studies reveal good thermal stability. The dopants increase the hardness value of the material, which also depends on the concentration of the dopants. Amino acids doping improved the NLO properties. The detailed results on the spectral parameters, habit modifications and constant values will be presented.

  7. Polarization reversal and ferroelectric domain structure observed in electroded cesium dihydrogen phosphate crystals using an X-ray anomalous dispersion effect

    International Nuclear Information System (INIS)

    Ozaki, Toru; Amau, Toshirou; Kawata, Hiroshi; Mizuno, Kaoru; Mori, Koichi.

    1997-01-01

    We have carried out an X-ray intensity measurement and X-ray topography on electroded b plates of ferroelectric cesium dihydrogen phosphate, CsH 2 PO 4 (CDP), using a synchrotron radiation with a wavelength of 2.482 A above the Cs L 3 -absorption edge. We have found that integrated intensities I(150) and I(1-bar5-bar0) show an anomalously large breakdown of Friedel's law, I(150)/I(1-bar5-bar0)=10.4 at 125 K, and display a ferroelectric hysteresis loop. The hysteresis loop determines that spontaneous polarization is antiparallel to the b axes set in both ferroelectric crystal structures related by inversions. The (150) diffraction topography shows that a single domain turns into a lamellar domain structure without fractal aspects after short-circuiting the b plate. The atomic displacement associated with polarization reversal is shown in a crystal structure model of 180deg domains observed in the X-ray topography. (author)

  8. Phosphate limitation in biological rapid sand filters used to remove ammonium from drinking water

    DEFF Research Database (Denmark)

    Lee, Carson Odell; Albrechtsen, Hans-Jørgen; Smets, Barth F.

    2013-01-01

    Removing ammonium from drinking water is important for maintaining biological stability in distribution systems. This is especially important in regions that do not use disinfectants in the treatment process or keep a disinfectant residual in the distribution system. Problems with nitrification c...... a pilot scale sand column which initial analysis confirmed performed similarly to the full scale filters. Long term increased ammonium loads were applied to the pilot filter both with and without phosphate addition. Phosphate was added at a concentration of 0.5 mg PO4-P/L to ensure...

  9. Phonon assisted electronic transition in telluric acid ammonium phosphate single crystals

    Science.gov (United States)

    El-Muraikhi, M.; Kassem, M. E.; Al-Houty, L.

    The effect of gamma-irradiation on the absorption optical spectra of telluric acid ammonium phosphate single crystals (TAAP) has been studied, in the wave length of 200-600 nm, for samples irradiated by various doses up to 10 Mrad. The results show that the electron phonon coupling constant increases with the irradiation dose.

  10. Automatized sspKa measurements of dihydrogen phosphate and Tris(hydroxymethyl) aminomethane in acetonitrile/water mixtures from 20 to 60°C.

    Science.gov (United States)

    Acquaviva, A; Tascon, M; Padró, J M; Gagliardi, L G; Castells, C B

    2014-09-01

    We measured pKa values of Tris(hydroxymethyl)aminomethane and dihydrogen phosphate; both are commonly used to prepare buffers for reverse-phase liquid chromatography (RPLC), in acetonitrile/water mixtures from 0% to 70% (v/v) (64.6% (w/w)) acetonitrile and at 20, 30, 40, 50, and 60°C. The procedure is based on potentiometric measurements of pH of buffer solutions of variable solvent compositions using a glass electrode and a novel automated system. The method consists in the controlled additions of small volumes of a thermostated solution from an automatic buret into another isothermal solution containing exactly the same buffer-component concentrations, but a different solvent composition. The continuous changes in the solvent composition induce changes in the potentials. Thus, only two sequences of additions are needed: increasing the amount of acetonitrile from pure water and decreasing the content of acetonitrile from 70% (v/v) (64.6% (w/w)). In the procedure with homemade apparatus, times for additions, stirring, homogenization, and data acquisition are entirely controlled by software programmed for this specific routine. This rapid, fully automated method was applied to acquire more than 40 potential data covering the whole composition range (at each temperature) in about two hours and allowed a systematic study of the effect of temperature and acetonitrile composition on acid-base equilibria of two widely used substances to control pH close to 7. The experimental pKa results were fitted to empirical functions between pKa and temperature and acetonitrile composition. These equations allowed predictions of pKa to estimate the pH of mixtures at any composition and temperature, which would be very useful, for instance, during chromatographic method development. Copyright © 2014 Elsevier B.V. All rights reserved.

  11. Synthesis and characterization of ammonium phosphate fertilizers with boron

    Directory of Open Access Journals (Sweden)

    ANGELA MAGDA

    2010-07-01

    Full Text Available The concentration of boron, an essential micronutrient for plants, presents a narrow range between deficiency and toxicity. In order to provide the boron requirement for plants, and to avoid toxicity problems, boron compounds are mixed with basic fertilizers. Sodium borate pentahydrate was used as a boron source. Ammonium orthophosphates fertilizers with boron were prepared by neutralizing phosphoric acid with ammonia and addition of variable amounts of sodium tetraborate pentahydrate to the reaction mixture at a NH3:H3PO4 molar ratio of 1.5. The fertilizers obtained with boron contents ranging from 0.05 to 1 % (w/w were fully characterized by chemical analysis, thermal analysis, X-ray diffraction and infrared spectrophotometry. The studies showed that up to 500 °C, regardless of the boron content, no significant changes concerning thermal stability and nutritional properties occurred. Above 500 °C, an increase of thermal stability with an increase of the boron content was observed. X-Ray diffraction of a heat-treated sample containing 5 % (w/w boron indicated the appearance of boron orthophosphate, BPO4, as a new crystalline phase, and the disappearance of the previous structures above 500 °C, which explains the increase in thermal stability.

  12. Occupational exposures in two industrial plants devoted to the production of ammonium phosphate fertilisers

    International Nuclear Information System (INIS)

    Bolívar, J P; Mosqueda, F; Gázquez, M J; López-Coto, I; Vaca, F; García-Tenorio, R; Adame, J A

    2013-01-01

    In order to fill a gap in the open literature, occupational exposures and activity concentrations have been assessed in two NORM industrial plants, located in the south-west of Spain, devoted to the production of mono-ammonium phosphate (MAP) and di-ammonium phosphate (DAP) fertilisers. The annual effective doses received by the workers from these plants are clearly below 1 mSv yr −1 and the contribution due to external radiation is similar to that due to inhalation. The contribution to the maximum effective doses due to inhalation of particulate matter has been estimated to be about 0.12 mSv yr −1 , while the 222 Rn concentrations inside the plants are of no concern. Consequently, no additional actions or radiological protection measures need to be taken to decrease the natural radiation received by the workers in these facilities. (paper)

  13. Evaluation of ammonium nitrate phosphate (Suphala) having different water soluble phosphorus levels on black soils

    International Nuclear Information System (INIS)

    Deo Dutt; Mutatkar, V.K.; Chapke, V.G.

    1974-01-01

    Efficiency of the laboratory prepared 32 P tagged ammonium nitrate phosphate (Suphala) varying in water soluble P was studied both on calcareous and non-calcareous soils of Maharashtra for bajra and wheat crops under greenhouse conditions. The results revealed a significant increase in dry matter production and uptake of total and fertilizer P with Suphala containing 30-32% water-soluble phosphorus. (author)

  14. 32P tracer studies on the efficiency of ammonium nitrate phosphates and polyphosphates for growing rice on different soil types

    International Nuclear Information System (INIS)

    Sadanandan, A.K.; Mohanty, S.K.; Patnaik, S.; Mistry, K.B.

    1980-01-01

    A pot experiment was conducted with 32 P tagged phosphates to evaluate the efficiency of ammonium nitrate phosphate containing 30, 50 and 70 percent of P in the water soluble form, tri- and tetra-ammonium pyrophosphate, as compared with mono-ammonium ortho-phosphate (MAP) for growing rice on red, laterite and black soils, with regard to recovery of applied P in soil, dry matter production and utilization of applied P by crop at flowering and grain and straw yield at harvest. Ammonium nitrate phosphates containing 50 percent or more of P in the water soluble form could be used for growing rice on all soil types. The pyrophosphates were as efficient as MAP on soils having pH 6.2 and above but less efficient in soils of lower pH. (author)

  15. Synthesis and characterization of the aluminium phosphates modified with ammonium, calcium and molybdenum by hydrothermal method

    Directory of Open Access Journals (Sweden)

    Łuczka Kinga

    2016-06-01

    Full Text Available Synthesis and characterization of the aluminum phosphates modified with ammonium, calcium and molybdenum were conducted. The influence of process parameters (reactive pressure and molar ratios in the reaction mixture were studied. The contents of the individual components in the products were in the range of: 10.97–17.31 wt% Al, 2.65–13.32 wt% Ca, 0.70–3.11 wt% Mo, 4.36–8.38 wt% NH3, and 35.12–50.54 wt% P2O5. The materials obtained in the experiments were characterized by various physicochemical parameters. The absorption oil number was in the range from 67 to 89 of oil/100 g of product, the surface area was within the range of 4–76 m2/g, whereas the average particle size of products reached 282–370 nm. The Tafel tests revealed comparable anticorrosive properties of aluminum phosphates modified with ammonium, calcium, molybdenum in comparison with commercial phosphate.

  16. Hierarchical one-dimensional ammonium nickel phosphate microrods for high-performance pseudocapacitors

    CSIR Research Space (South Africa)

    Raju, K

    2015-12-01

    Full Text Available :17629 | DOI: 10.1038/srep17629 www.nature.com/scientificreports Hierarchical One-Dimensional Ammonium Nickel Phosphate Microrods for High-Performance Pseudocapacitors Kumar Raju1 & Kenneth I. Ozoemena1,2 High-performance electrochemical capacitors... OPEN w w w . n a t u r e . c o m / s c i e n t i f i c r e p o r t s / 2S C I E N T I F I C REPORTS | 5:17629 | DOI: 10.1038/srep17629 Hierarchical 1-D and 2-D materials maximize the supercapacitive properties due to their unique ability to permit ion...

  17. Evaluation and thermodynamic calculation of ureolytic magnesium ammonium phosphate precipitation from UASB effluent at pilot scale.

    Science.gov (United States)

    Desmidt, E; Ghyselbrecht, K; Monballiu, A; Verstraete, W; Meesschaert, B D

    2012-01-01

    The removal of phosphate as magnesium ammonium phosphate (MAP, struvite) has gained a lot of attention. A novel approach using ureolytic MAP crystallization (pH increase by means of bacterial ureases) has been tested on the anaerobic effluent of a potato processing company in a pilot plant and compared with NuReSys(®) technology (pH increase by means of NaOH). The pilot plant showed a high phosphate removal efficiency of 83 ± 7%, resulting in a final effluent concentration of 13 ± 7 mg · L(-1) PO(4)-P. Calculating the evolution of the saturation index (SI) as a function of the remaining concentrations of Mg(2+), PO(4)-P and NH(4)(+) during precipitation in a batch reactor, resulted in a good estimation of the effluent PO(4)-P concentration of the pilot plant, operating under continuous mode. X-ray diffraction (XRD) analyses confirmed the presence of struvite in the small single crystals observed during experiments. The operational cost for the ureolytic MAP crystallization treating high phosphate concentrations (e.g. 100 mg · L(-1) PO(4)-P) was calculated as 3.9 € kg(-1) P(removed). This work shows that the ureolytic MAP crystallization, in combination with an autotrophic nitrogen removal process, is competitive with the NuReSys(®) technology in terms of operational cost and removal efficiency but further research is necessary to obtain larger crystals.

  18. Dental plaque microcosm biofilm behavior on calcium phosphate nanocomposite with quaternary ammonium.

    Science.gov (United States)

    Cheng, Lei; Weir, Michael D; Zhang, Ke; Wu, Eric J; Xu, Sarah M; Zhou, Xuedong; Xu, Hockin H K

    2012-08-01

    Half of dental restorations fail in 10 years, with secondary caries as the main reason. Calcium phosphate composites could remineralize tooth lesions. The objectives of this study were to: (1) impart antibacterial activity to a composite with nanoparticles of amorphous calcium phosphate (NACP); and (2) investigate the effect of quaternary ammonium dimethacrylate (QADM) on mechanical and dental plaque microcosm biofilm properties for the first time. The NACP and glass particles were filled into a dental resin that contained bis(2-methacryloyloxy-ethyl) dimethyl-ammonium bromide, the QADM. NACP nanocomposites containing 0%, 7%, 14%, and 17.5% of QADM by mass, respectively, were photo-cured. A commercial composite with no antibacterial activity was used as control. Mechanical properties were measured in three-point flexure. A human saliva microcosm model was used to grow biofilms on composites. Live/dead assay, metabolic activity, colony-forming unit (CFU) counts, and lactic acid production of biofilms on the composites were measured. Increasing QADM mass fraction monotonically reduced the biofilm viability, CFU and lactic acid. Biofilms on NACP nanocomposite with 17.5% QADM had metabolic activity that was 30% that on a commercial composite control (pbacterial cells with normal short-rod shapes, while some cells on NACP-QADM nanocomposites disintegrated into pieces. Adding QADM to NACP did not decrease the composite strength and elastic modulus, which matched (p>0.1) those of a commercial composite without Ca-PO(4) or antibacterial activity. A dental plaque microcosm model was used to evaluate the novel NACP-QADM nanocomposite. The nanocomposite greatly reduced the biofilm viability, metabolic activity and lactic acid, while its mechanical properties matched those of a commercial composite. NACP-QADM nanocomposite with calcium phosphate fillers, good mechanical properties and a strong antibacterial activity may have potential for anti-biofilm and anti

  19. Formation Mechanism of Magnesium Ammonium Phosphate Stones: A Component Analysis of Urinary Nanocrystallites

    Directory of Open Access Journals (Sweden)

    Xin-Yuan Sun

    2015-01-01

    Full Text Available The components of urinary nanocrystallites in patients with magnesium ammonium phosphate (MAP stones were analyzed by X-ray diffraction (XRD, Fourier-transform infrared (FT-IR spectrometer, high-resolution transmission electron microscopy (HRTEM, selected area electron diffraction (SAED, fast Fourier transformation (FFT, and energy-dispersive X-ray spectroscopy (EDS. The main components of the stones were MAP hexahydrate (MAP·6H2O, magnesium hydrogen phosphate trihydrate (MgHPO4·3H2O, and a small amount of calcium phosphate (CaP, while the main components of urinary nanocrystallites were MgHPO4·3H2O, CaP, and MAP monohydrate (MAP·H2O. MAP·H2O induced the formation of MAP stones as seed crystals. MgHPO4·3H2O was accompanied by the appearance of MAP·6H2O. The formation mechanism of MAP stones and influencing factors were discussed on the basis of the components of urine nanocrystallites. A model diagram of MAP stone formation was also put forward based on the results. Formation of MAP stones was closely related to the presence of high amounts of MAP crystallites in urine. Urinary crystallite condition and changes in urine components could indicate the activity of stone diseases.

  20. Radio phosphorus kinetics in the blood of sheep supplemented with dicalcium phosphate, mono ammonium phosphate, triple superphosphate and Tapira rock phosphate

    International Nuclear Information System (INIS)

    Abdalla, A.L.

    1992-01-01

    With the aim to study the kinetics of radio phosphorus ( 32 P) in the blood of animals supplemented with dicalcium phosphate (BIC), mono ammonium phosphate (MAP), triple superphosphate (SPT) and Tapira rock phosphate (TAP), 32 male sheep were kept in metabolic cages at the Animal Science Section / CENA - USP. Plasma was obtained by centrifugation and the specific activity, rate of disappearance and half life of 32 P in plasma were determined. In the red blood cells were determined the uptake rate of the radioisotope, the rate of disappearance and half life of 32 P up taken. It was observed a statistical significant difference (p 32 P in the plasma and erythrocytes. The specific activity and half life of 32 P in the plasma were statistically different (p<0,10) among sheep receiving the different phosphorus sources; the same was observed in respect to the red blood cells. It was concluded that the supplemented phosphorus source given in the diet of sheep may affect the kinetics of the radio phosphorus in the blood after been intravenously injected. (author)

  1. Photometric Determination of Ammonium and Phosphate in Seawater Medium Using a Microplate Reader.

    Science.gov (United States)

    Ruppersberg, Hanna S; Goebel, Maren R; Kleinert, Svea I; Wünsch, Daniel; Trautwein, Kathleen; Rabus, Ralf

    2017-01-01

    To more efficiently process the large sample numbers for quantitative determination of ammonium (NH4+) and phosphate (orthophosphate, PO43-) generated during comprehensive growth experiments with the marine Roseobacter group member Phaeobacter inhibens DSM 17395, specific colorimetric assays employing a microplate reader (MPR) were established. The NH4+ assay is based on the reaction of NH4+ with hypochlorite and salicylate, yielding a limit of detection of 14 µM, a limit of quantitation of 36 µM, and a linear range for quantitative determination up to 200 µM. The PO43-assay is based on the complex formation of PO43- with ammonium molybdate in the presence of ascorbate and zinc acetate, yielding a limit of detection of 13 µM, a limit of quantitation of 50 µM, and a linear range for quantitative determination up to 1 mM. Both MPR-based assays allowed for fast (significantly lower than 1 h) analysis of 21 samples plus standards for calibration (all measured in triplicates) and showed only low variation across a large collection of biological samples. © 2017 S. Karger AG, Basel.

  2. Immobilisation of radio cesium loaded ammonium molybdo phosphate in glass matrices

    International Nuclear Information System (INIS)

    Yalmali, Vrunda S.; Singh, I.J.; Sathi Sasidharan, N.; Deshingkar, D.S.

    2004-11-01

    Long half life and easy availability from high level wastes make 137 Cesium most economical radiation source. High level liquid waste processing for 137 Cesium removal has become easier due to development of Cesium specific granulated ammonium molybdophosphate (AMP) composite. In such applications, resulting spent composite AMP itself represents high active solid waste and immobilization of these materials in cement may not be acceptable. Studies on immobilization of 137 Cs loaded AMP were taken up in order to achieve twin goals of increasing safety and minimizing processing costs of the final matrix. Studies indicated that phosphate modified sodium borosilicate SPNM glasses prepared under usual oxidizing conditions are not suitable for immobilization of 137 Cs loaded on AMP .Phosphate glasses containing Na 2 O, P 2 O 5 , B 2 O 3 , Fe 2 O 3 , Al 2 O 3 and SiO 2 as major constituents are capable of incorporating 6 to 8 % AMP. The Normalized Leach rates of these glasses for sodium, cesium, boron and silica are 10 -4 to 10 -6 gm/cm 2 /day which are comparable to or better than those reported for NBS glasses incorporating HLW. Homogeneity of the final matrix was confirmed by x-ray diffraction analysis. Further studies on characterization of these glasses would establish their acceptability. (author)

  3. Improved Spectra for MALDI MSI of Peptides Using Ammonium Phosphate Monobasic in MALDI Matrix.

    Science.gov (United States)

    Ucal, Yasemin; Ozpinar, Aysel

    2018-05-10

    MALDI mass spectrometry imaging (MSI) enables analysis of peptides along with histology. However, there are several critical steps in MALDI MSI of peptides, one of which is spectral quality. Suppression of MALDI matrix clusters by the aid of ammonium salts in MALDI experiments is well-known. It is asserted that addition of ammonium salts dissociates potential matrix adducts and thereafter decreases matrix cluster formation. Consequently, MALDI MS sensitivity and mass accuracy increases. Up to our knowledge, a limited number of MALDI MSI studies used ammonium salts as matrix additives to suppress matrix clusters and enhance peptide signals. In this work, we investigated the effect of ammonium phosphate monobasic (AmP) as alpha-cyano-4-hydroxycinnamic acid (α-CHCA) matrix additive in MALDI MSI of peptides. Prior to MALDI MSI, the effect of varying concentrations of AmP in α-CHCA were assessed in bovine serum albumin (BSA) tryptic digests and compared with the control (α-CHCA without AmP). Based on our data, the addition of AmP as matrix additive decreased matrix cluster formation regardless of its concentration and, specifically 8 mM AmP and 10 mM AmP increased BSA peptide signal intensities. In MALDI MSI of peptides, both 8 mM, and 10 mM AmP in α-CHCA improved peptide signals especially in the mass range of m/z 2000 to 3000. In particular, 9 peptide signals were found to have differential intensities within the tissues deposited with AmP in α-CHCA (AUC>0.60). To the best of our knowledge, this is the first MALDI MSI of peptides work investigating different concentrations of AmP as α-CHCA matrix additive in order to enhance peptide signals in formalin fixed paraffin embedded (FFPE) tissues. Further, AmP as part of α-CHCA matrix could enhance protein identifications and support MALDI MSI based proteomic approaches. This article is protected by copyright. All rights reserved.

  4. 磷酸二氢钙与生物质共热解提高生物炭固碳效果%Biomass co-pyrolysis with calcium dihydrogen phosphate improving carbon fixation of biochar

    Institute of Scientific and Technical Information of China (English)

    李飞跃; 张丽; 李孝良; 谢越; 王艳; 汪建飞

    2016-01-01

    Turning biomass wastes into biochar under low temperature and limited oxygen conditions has recently proven as a promising approach for long term carbon sequestration. In order to reveal the effects of mineral addition which is a pretreatment of biochar production on carbon retention and stability of biochar and provide an creative idea for further improvement of carbon sequestration potential by turning biomass into biochar. Calcium dihydrogen phosphate using as a typical mineral was added to sawdust and dairy manure feedstock at the ratio of 20% for biochar formation through co-pyrolysis treatment under lab condition, a typical slow pyrolysis process, heated in a Muffle Furnace at a speed of approximately 20℃/min under limited oxygen and held at 200 to 500℃ with every other 100℃ for 1 h. Moreover, two reliable methods were applied to test biochar stability: One was a simulated long-term stability method using chemical oxidation treatment to assess the labile fraction of C in biochar samples after hydrogen peroxide (H2O2) oxidation, this method was to determine the chemical stability of biochar; The other was simulated mineralization experiment to test the biochar's microbe-resistance stability, this method was to evaluate the biological stability of biochar in terms of microbial mineralization rate under simulated soil microbial conditions in a lab-scale experiment. The carbon retention was defined as the proportion of the original carbon, which was from plant photosynthesis by sequestrating the CO2 from atmosphere in feedstock, retained in the biochar after the pyrolysis. Compared with the original biochar, modified biochar produced with calcium dihydrogen phosphate addition to sawdust and dairy manure were increased by 31.3% and 26.1%, respectively; With H2O2 oxidation, the carbon loss of modified biochar produced with calcium dihydrogen phosphate addition to sawdust was reduced by 93.1%, compared with its unmodified biochar. However, the carbon loss of

  5. Thermodynamic properties of solutions of sodium di-hydrogen phosphate in (1-propanol + water) mixed-solvent media over the temperature range of (283.15 to 303.15) K

    International Nuclear Information System (INIS)

    Sadeghi, Rahmat; Parhizkar, Hana

    2008-01-01

    The apparent molar volume and apparent molar isentropic compressibility of solutions of sodium di-hydrogen phosphate (NaH 2 PO 4 ) in (1-propanol + water) mixed-solvent media with alcohol mass fractions of 0.00, 0.05, 0.10, and 0.15 are reported over the range of temperature (283.15 to 303.15) K at 5 K intervals. The results were fitted to a Redlich-Mayer type equation from which the apparent molar volume and apparent molar isentropic compressibility of the solutions at the infinite dilution were also calculated at the working temperature. The results show a positive transfer volume of NaH 2 PO 4 from an aqueous solution to an aqueous 1-propanol solution. The apparent molar isentropic compressibility of NaH 2 PO 4 in aqueous 1-propanol solutions is negative and it increases with increasing the concentration of NaH 2 PO 4 , 1-propanol, and temperature. Electrical conductivity and refractive index of the solutions are also studied at T = 298.15 K. The effects of the electrolyte concentration and relative permittivity of the medium on the molar conductivity were also investigated

  6. Sorption of ammonium and phosphate from aqueous solution by biochar derived from phytoremediation plants

    Institute of Scientific and Technical Information of China (English)

    Zheng ZENG; Muhammad Tariq RAFIQ; Song-da ZHANG; Ting-qiang LI; Feng-liang ZHAO; Zhen-li HE; He-ping ZHAO; Xiao-e YANG; Hai-long WANG; Jing ZHAO

    2013-01-01

    The study on biochar derived from plant biomass for environmental applications is attracting more and more attention. Twelve sets of biochar were obtained by treating four phytoremediation plants, Salix rosthorni Seemen, Thalia dealbata, Vetiveria zizanioides, and Phragmites sp., sequential y through pyrolysis at 500 °C in a N2 environ-ment, and under different temperatures (500, 600, and 700 °C) in a CO2 environment. The cation exchange capacity and specific surface area of biochar varied with both plant species and pyrolysis temperature. The magnesium (Mg) content of biochar derived from T. dealbata (TC) was obviously higher than that of the other plant biochars. This bi-ochar also had the highest sorption capacity for phosphate and ammonium. In terms of biomass yields, adsorption capacity, and energy cost, T. dealbata biochar produced at 600 °C (TC600) is the most promising sorbent for removing contaminants (N and P) from aqueous solution. Therefore, T. dealbata appears to be the best candidate for phyto-remediation application as its biomass can make a good biochar for environmental cleaning.

  7. Dibasic Ammonium Phosphate Application Enhances Aromatic Compound Concentration in Bog Bilberry Syrup Wine

    Directory of Open Access Journals (Sweden)

    Shao-Yang Wang

    2016-12-01

    Full Text Available A nitrogen deficiency always causes bog bilberry syrup wine to have a poor sensory feature. This study investigated the effect of nitrogen source addition on volatile compounds during bog bilberry syrup wine fermentation. The syrup was supplemented with 60, 90, 120 or 150 mg/L dibasic ammonium phosphate (DAP before fermentation. Results showed that an increase of DAP amounts accelerated fermentation rate, increased alcohol content, and decreased sugar level. Total phenol and total flavonoid content were also enhanced with the increase of DAP amounts. A total of 91 volatile compounds were detected in the wine and their concentrations were significantly enhanced with the increase of DAP. Ethyl acetate, isoamyl acetate, phenethyl acetate, ethyl butanoate, ethyl hexanoate, ethyl octanoate, ethyl decanoate, isobutanol, isoamyl alcohol, levo-2,3-butanediol, 2-phenylethanol, meso-2,3-butanediol, isobutyric acid, hexanoic acid, and octanoic acid exhibited a significant increase of their odor activity value (OAV with the increase of DAP amounts. Bog bilberry syrup wine possessed fruity, fatty, and caramel flavors as its major aroma, whereas a balsamic note was the least present. The increase of DAP amounts significantly improved the global aroma attributes, thereby indicating that DAP supplementation could promote wine fermentation performance and enhance the sensory quality of bog bilberry syrup wine.

  8. /sup 32/P tracer studies on the efficiency of ammonium nitrate phosphates and polyphosphates for growing rice on different soil types

    Energy Technology Data Exchange (ETDEWEB)

    Sadanandan, A K; Mohanty, S K; Patnaik, S [Central Rice Research Inst., Cuttack (India); Mistry, K B [Bhabha Atomic Research Centre, Bombay (India). Biology and Agriculture Div.

    1980-12-01

    A pot experiment was conducted with /sup 32/P tagged phosphates to evaluate the efficiency of ammonium nitrate phosphate containing 30, 50 and 70 percent of P in the water soluble form, tri- and tetra-ammonium pyrophosphate, as compared with mono-ammonium ortho-phosphate (MAP) for growing rice on red, laterite and black soils, with regard to recovery of applied P in soil, dry matter production and utilization of applied P by crop at flowering and grain and straw yield at harvest. Ammonium nitrate phosphates containing 50 percent or more of P in the water soluble form could be used for growing rice on all soil types. The pyrophosphates were as efficient as MAP on soils having pH 6.2 and above but less efficient in soils of lower pH.

  9. Antibacterial and remineralizing orthodontic adhesive containing quaternary ammonium resin monomer and amorphous calcium phosphate nanoparticles.

    Science.gov (United States)

    Liu, Yan; Zhang, Ling; Niu, Li-Na; Yu, Tao; Xu, Hockin H K; Weir, Michael D; Oates, Thomas W; Tay, Franklin R; Chen, Ji-Hua

    2018-05-01

    To evaluate the bonding performance, antibacterial activity, and remineralization effect on enamel of the orthodontic adhesive containing MAE-DB and NACP. Eighty non-carious human premolars were divided into 3 groups: Transbond XT (TB), PEHB + 5% MAE-DB (PD), and PEHB + 40% NACP + 5% MAE-DB (PND). Premolars were bonded with orthodontic brackets, the first subgroup (n = 10) and the second subgroup (n = 10) were subjected to shear bond strength testing after immersed in water for 1 day and in demineralization solution for 28 days respectively and then tested surface roughness, while the third subgroup (n = 6) was used for microhardness evaluation after aged in demineralization solution for 28 days. For each adhesive, fifty disk samples were prepared for antibacterial study. Specimens measuring 12 mm × 2 mm × 2 mm were fabricated for ion release test. Bond strengths were in the order TB = PND > PND = PD for "1-day in water", and in the order TB = PND > PD for "28-days in pH 4 solution". No significant difference in the ARI scores for the three adhesive. Numerous bacteria adhered to TB surface, while PD and PND had minimal bacterial growth and activity. PND showed high levels of Ca and P ions release and enamel hardness. The surface roughness of enamel in PND was much lower than TB and PD and showed no significant difference with the sound, control enamel. PND adhesive with 5% MAE-DB and 40% NACP exhibits antibacterial and remineralizing capabilities, and did not adversely affect bond strength compared to commercial adhesive. Novel adhesive containing quaternary ammonium monomer and nano-amorphous calcium phosphate represents a promising candidate in combating enamel white spot lesions and even dental caries. Copyright © 2018 Elsevier Ltd. All rights reserved.

  10. The diagnostic value of 99TcM-2-(2-methyl-5-nitro-1H-imidazol-1-yl) ethyl dihydrogen phosphate hypoxia imaging and its evaluation performance for radiotherapy efficacy in non-small-cell lung cancer.

    Science.gov (United States)

    Yang, Yongkun; Han, Gaohua; Xu, Wansong

    2016-01-01

    This study was designated to assess the diagnostic value of 99 Tc M -2-(2-methyl-5-nitro-1 H -imidazol-1-yl) ethyl dihydrogen phosphate ( 99 Tc M -MNLS) hypoxia imaging and its evaluation performance for radiotherapy efficacy in patients with non-small-cell lung cancer (NSCLC). A total of 61 patients with NSCLC were selected for this study. All patients were injected with 99 Tc M -MNLS within 1 week prior to radiotherapy and they were injected with 99 Tc M -MNLS again 3 months after radiotherapy. Qualitative analysis along with semiquantitative analysis results were obtained from hypoxia imaging. Meanwhile, the effect of radiotherapy on patients with NSCLC was evaluated based on the solid tumor curative effect evaluation standard. Finally, SPSS 19.0 statistical software was implemented for statistical analysis. There was no significant difference in age or sex between the NSCLC patient group and benign patient group ( P >0.05). 99 Tc M -MNLS was selectively concentrated in tumor tissues with a clear imaging in 24 hours. Results from both qualitative analysis and semiquantitative analysis indicated that the sensitivity and specificity of 99 Tc M -MNLS hypoxia imaging in diagnosing NSCLC were 93.8% and 84.6% and 72.9% and 100%, respectively. Moreover, the receiver operating characteristic curve provided evidence that 99 Tc M -MNLS hypoxia imaging was a powerful diagnostic tool in distinguishing malignant lung cancer from benign lesions. As suggested by 24-hour imaging, the tumor-to-normal ratio of patients in the 99 Tc M -MNLS high-intake group and low-intake group had a decline of 24.7% and 14.4% after radiotherapy, respectively. The decline in the tumor-to-normal ratio between the two dosage groups was significantly different ( P evaluating therapeutic effects of radiotherapy on patients with NSCLC.

  11. Ammonium, Nitrate, and Phosphate Sorption to and Solute Leaching from Biochars Prepared from Corn Stover ( L.) and Oak Wood ( spp.).

    Science.gov (United States)

    Hollister, C Colin; Bisogni, James J; Lehmann, Johannes

    2013-01-01

    Biochar (BC) was evaluated for nitrogen (N) and phosphorus (P) removal from aqueous solution to quantify its nutrient pollution mitigation potential in agroecosystems. Sorption isotherms were prepared for solutions of ammonium (NH), nitrate (NO), and phosphate (PO-P) using BC of corn ( L.) and oak ( spp.) feedstock, each pyrolyzed at 350 and 550°C highest treatment temperature (HTT). Sorption experiments were performed on original BC as well as on BC that went through a water extraction pretreatment (denoted WX-BC). Ammonium sorption was observed for WX-Oak-BC and WX-Corn-BC, and Freundlich model linearization showed that a 200°C increase in HTT resulted in a 55% decrease in * values for WX-Oak-BC and a 69% decrease in * for WX-Corn-BC. Nitrate sorption was not observed for any BC. Removing metals by water extraction from WX-Oak-350 and WX-Oak-550 resulted in a 25 to 100% decrease in phosphate removal efficiency relative to original Oak-350 and Oak-550, respectively. No PO-P sorption was observed using any Corn-BC. Calcium (Ca) leached from BC produced at 550°C was 63 and 104% higher than from BC produced at 350°C for corn and oak, respectively. Leaching of P was two orders of magnitude lower in WX-Oak-BC than in WX-Corn-BC, concurrent with similar difference in magnesium (Mg). Nitrate and NH leaching from consecutive water extractions of all tested BCs was mostly below detection limits. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

  12. Ammonium and phosphate enrichment across the dry-wet transition and their ecological relevance in a subtropical reservoir, China.

    Science.gov (United States)

    Mo, Qiongli; Chen, Nengwang; Zhou, Xingpeng; Chen, Jixin; Duan, Shuiwang

    2016-07-13

    Small river reservoirs are widespread and can be ecologically sensitive across the dry-wet transition under monsoon climate with respect to nutrient loading and phenology. Monthly sampling and high-frequency in situ measurements were conducted for a river reservoir (southeast China) in 2013-2014 to examine the seasonal pattern of nutrients and phytoplankton. We found that nutrient concentrations were runoff-mediated and determined by watershed inputs and, in some cases, by internal cycling depending on hydrology and temperature. Ammonium and phosphate were relatively enriched in February-March (a transitional period from dry/cold to wet/hot climate), which can be ascribed to initial flushing runoff from human/animal waste and spring fertilizer use. A phytoplankton bloom (mainly Chlorophyta) occurred during April after a surge of water temperature, probably due to the higher availability of inorganic nutrients and sunlight and suitable hydraulic residence time (medium flow) in the transitional period. The concentration of phytoplankton was low during May-June (wet-hot climate) when the concentrations of total suspended matter (TSM) were highest, likely owing to the "shading" effect of TSM and turbulence of high flow conditions. Nutrient-algae shifts across the dry-wet season and vertical profiles suggested that algal blooms seem to be fueled primarily by phosphate and ammonium rather than nitrate. Current findings of a strong temporal pattern and the relationship between physical parameters, nutrient and biota would improve our understanding of drivers of change in water quality and ecosystem functions with dam construction.

  13. Separation of radio cesium from PUREX feed solution by sorption on composite ammonium molybdo phosphate (AMP)

    International Nuclear Information System (INIS)

    Singh, I.J.; Achuthan, P.V.; Jain, S.; Janardanan, C.; Gopalakrishnan, V.; Wattal, P.K.; Ramanujam, A.

    2001-01-01

    Composite AMP exchanger was developed and evaluated for separation of radio cesium from dissolver solutions of PUREX process using a column experiment. The composite shows excellent sorption of radio cesium from dissolver solutions without any loss of plutonium and uranium. The removal of radio cesium from dissolver solutions will help in lowering the degradation of tri-n-butyl phosphate (TBP) in the solvent extraction process and will also help in reducing the radiation related problems. (author)

  14. Ammonium iron(III phosphate(V fluoride, (NH40.5[(NH40.375K0.125]FePO4F, with ammonium partially substituted by potassium

    Directory of Open Access Journals (Sweden)

    Lei Wang

    2009-01-01

    Full Text Available The title compound, ammonium potassium iron(III phosphate fluoride, (NH40.875K0.125FePO4F, is built from zigzag chains ∞1{[FeO4F2]7−}, with Fe3+ in a distorted octahedral coordination, extending along both the [011] and [0overline{1}1] directions. These chains are made up of alternating trans-[FeO4F2] and cis-[FeO4F2] octahedra via shared F-atom corners, and are linked by PO4 tetrahedra, resulting in an open-framework structure with channels along the [010] and [100] directions. There are two crystallographically independent ammonium sites: one in the [010] channels and the other, partially substituted by K+ ions, in the [100] channels. The ammonium in the [010] channels is fixed to the framework via eight hydrogen bonds (six N—H...O and two N—H...F.

  15. Flame retardancy of polyamide 6 hybrid fibers: Combined effects of α-zirconium phosphate and ammonium sulfamate

    Directory of Open Access Journals (Sweden)

    Hengxue Xiang

    2017-06-01

    Full Text Available Synergistic effect between α-zirconium phosphate (α-ZrP and ammonium sulfamate (AS for enhanced flame retardant properties of Polyamide 6 (PA6 was investigated by using oxygen index instrument, cone calorimeter, thermogravimetric analyzer (TGA, Instron universal test machine and scanning electron microscopy (SEM. PA6/AS/α-ZrP ternary hybrid materials with various contents of α-ZrP and AS were fabricated by melt-mixing method. The result from flammability indicated that the Limiting oxygen index (LOI and Underwriters Laboratories-94 (UL-94 rating of PA6/AS/α-ZrP were significantly accelerated under the coordinating function of α-ZrP and AS. Moreover, the thermal stability for PA6/AS/α-ZrP studied by TGA also demonstrated this synergistic effect between α-ZrP and AS on the heat resistance. The effects of the usage amount of α-ZrP and AS on mechanical properties were analyzed by using uniaxial tensile test. It was found that the addition of AS provided negative effects on the tensile strength of PA6/AS/α-ZrP, however, the adverse trends that mentioned above could be overcome by using the well dispersed α-ZrP.

  16. Effect of Pyrite on Thiosulfate Leaching of Gold and the Role of Ammonium Alcohol Polyvinyl Phosphate (AAPP

    Directory of Open Access Journals (Sweden)

    Xiaoliang Liu

    2017-07-01

    Full Text Available The effect of pyrite and the role of ammonium alcohol polyvinyl phosphate (AAPP during gold leaching in ammoniacal thiosulfate solutions were investigated using pure gold foils. The results showed that pyrite catalyzed the decomposition and also significantly increased the consumption of thiosulfate. This detrimental effect became more severe with increasing pyrite content. Further, the presence of pyrite also substantially slowed the gold leaching kinetics and reduced the overall gold dissolution. The reduction in gold dissolution was found to be caused primarily by the surface passivation of the gold. The negative effects of pyrite, however, can be alleviated by the addition of AAPP. Comparison of zeta potentials of pyrite with and without AAPP suggests that AAPP had adsorbed on the surface of the pyrite and weakened the catalytic effect of pyrite on the thiosulfate decomposition by blocking the contact between the pyrite and thiosulfate anions. AAPP also competed with thiosulfate anions to complex with the cupric ion at the axial coordinate sites, and thus abated the oxidation of thiosulfate by cupric ions. Moreover, the indiscriminate adsorption of AAPP on the surfaces of gold and passivation species prevented the passivation of the gold surface by surface charge and electrostatic repulsion. Therefore, AAPP effectively stabilized the thiosulfate in the solution and facilitated the gold leaching in the presence of pyrite.

  17. True absorption of phosphorus from di calcium phosphate, mono ammonium phosphate, triple superphosphate and urea-phosphate in bovine by the radio phosphorus dilution technique

    International Nuclear Information System (INIS)

    Silva Filho, J.C. da.

    1990-01-01

    With the aim to study the utilization of alternative sources of phosphorus by ruminants. Twenty four males steers, with 250 Kg live weight and 18 months of age, were allocated in four groups of six animals each. The animals were housed in individual pens and received a diet containing chopped hay, corn and soybean meal, urea and mineral mixtures. The phosphate sources were added to supply 10 g of phosphorus per animal daily. The animals were injected intravenously and individually with 37 MBq of P-32 (N A 2 H P O 4 ) at the 20 th day of the experimental trial into the jugular vein. Blood and faces were collected and sampled at 24 hours intervals, for 8 days. Based on the specific activities in plasma and faces, the fecal endogenous loss and true phosphorus absorption were determined. (author)

  18. Efficiency of ammonium nitrate phosphates of varying water-soluble phosphorus content for rice and succeeding maize crop on contrasting soil types

    International Nuclear Information System (INIS)

    Bhujbal, B.M.; Mistry, K.B.; Chapke, V.G.; Mutatkar, V.K.

    1977-01-01

    Efficiency of ammonium nitrate phosphates (ANP) containing 30 and 50 percent of water-soluble phosphorus (W.S.P.) vis-a-vis that of entirely water-soluble monoammonium orthophosphate (MAP) for rice and succeeding maize crop on phosphate responsive laterite, red sandy loam (Chalka) and calcareous black soils was examined in greenhouse experiments. Data on dry matter yield, uptake of phosphorus, utilization of applied fertilizer, 'Effective Rate of Application' and 'Relative Efficiency percent' at flowering stage of rice indicated no significant differences between ammonium nitrate phosphate (30 percent and 50 percent water-soluble ohosphorus) and monoammonium orthophosphate (MAP) on laterits and natural red sandy loam soils. MAP was significantly superior to the two ANP fertilizers on calcareous black soil; no significant differences were observed between ANP (30 percent W.S.P.) and ANP (50 percent W.S.P.) on this soil. The succeeding maize crop grown up to flowering in the same pots indicated that the residual value of ANP (30 percent W.S.P.) was equal or superior to that of MAP on the laterits as well as calcareous black soil. No significant differences were detected between the residual values of the two water-solubility grades of ANP. Incubation under submerged conditions for periods upto 60 days showed that 0.5 M NaHCO 3 (pH 8.5) extractable phosphorus (plant-available phosphate) in the ANP (30 percent W.S.P.) treatment was, in general, equal to those in the MAP treatments in the laterite and red sandy loam but was significantly lower in the calcareous black soil. No marked differences were observed between the effects of the two ANP fertilizers. (author)

  19. Efficiency of ammonium nitrate phosphates of varying water-soluble phosphorus content for rice and succeeding maize crop on contrasting soil types. [/sup 32/P-labelled fertilizers

    Energy Technology Data Exchange (ETDEWEB)

    Bhujbal, B M; Mistry, K B [Bhabha Atomic Research Centre, Bombay (India). Biology and Agriculture Div.; Chapke, V G; Mutatkar, V K [Fertilizer Corp. of India Ltd., Bombay

    1977-09-01

    Efficiency of ammonium nitrate phosphates (ANP) containing 30 and 50 percent of water-soluble phosphorus (W.S.P.) vis-a-vis that of entirely water-soluble monoammonium orthophosphate (MAP) for rice and succeeding maize crop on phosphate responsive laterite, red sandy loam (Chalka) and calcareous black soils was examined in greenhouse experiments. Data on dry matter yield, uptake of phosphorus, utilization of applied fertilizer, 'Effective Rate of Application' and 'Relative Efficiency percent' at flowering stage of rice indicated no significant differences between ammonium nitrate phosphate (30 percent and 50 percent water-soluble ohosphorus) and monoammonium orthophosphate (MAP) on laterits and natural red sandy loam soils. MAP was significantly superior to the two ANP fertilizers on calcareous black soil; no significant differences were observed between ANP (30 percent W.S.P.) and ANP (50 percent W.S.P.) on this soil. The succeeding maize crop grown up to flowering in the same pots indicated that the residual value of ANP (30 percent W.S.P.) was equal or superior to that of MAP on the laterits as well as calcareous black soil. No significant differences were detected between the residual values of the two water-solubility grades of ANP. Incubation under submerged conditions for periods upto 60 days showed that 0.5 M NaHCO/sub 3/ (pH 8.5) extractable phosphorus (plant-available phosphate) in the ANP (30 percent W.S.P.) treatment was, in general, equal to those in the MAP treatments in the laterite and red sandy loam but was significantly lower in the calcareous black soil. No marked differences were observed between the effects of the two ANP fertilizers.

  20. Temperature dependence measurements and structural characterization of trimethyl ammonium ionic liquids with a highly polar solvent.

    Science.gov (United States)

    Attri, Pankaj; Venkatesu, Pannuru; Hofman, T

    2011-08-25

    We report the synthesis and characterization of a series of an ammonium ionic liquids (ILs) containing acetate, dihydrogen phosphate, and hydrogen sulfate anions with a common cation. To characterize the thermophysical properties of these newly synthesized ILs with the highly polar solvent N,N-dimethylformamide (DMF), precise measurements such as densities (ρ) and ultrasonic sound velocities (u) over the whole composition range have been performed at atmospheric pressure and over wide temperature ranges (25-50 °C). The excess molar volume (V(E)) and the deviation in isentropic compressibilities (Δκ(s)) were predicted using these temperature dependence properties as a function of the concentration of ILs. The Redlich-Kister polynomial was used to correlate the results. The ILs investigated in the present study included trimethylammonium acetate [(CH(3))(3)NH][CH(3)COO] (TMAA), trimethylammonium dihydrogen phosphate [(CH(3))(3)NH][H(2)PO(4)] (TMAP), and trimethylammonium hydrogen sulfate [(CH(3))(3)NH][HSO(4)] (TMAS). The intermolecular interactions and structural effects were analyzed on the basis of the measured and the derived properties. In addition, the hydrogen bonding between ILs and DMF has been demonstrated using semiempirical calculations with help of Hyperchem 7. A qualitative analysis of the results is discussed in terms of the ion-dipole, ion-pair interactions, and hydrogen bonding between ILs and DMF molecules and their structural factors. The influence of the anion of the protic IL, namely, acetate (CH(3)COO), dihydrogen phosphate (H(2)PO(4)), and hydrogen sulfate (HSO(4)), on the thermophysical properties is also provided. © 2011 American Chemical Society

  1. A new technique for the synthesis of ammonium phosphomolybdate: precipitation in resin support

    International Nuclear Information System (INIS)

    Matsuda, H.T.

    1977-01-01

    A technique for synthesizing ammonium molybdophosphate, an inorganic ion exchanger which retains selectively cesium-137 from a mixture of fission products, employing a strong anionic resin, saturated with molybdate anions, is presented. This method enables the precipitation of ammonium molybdophosphate directly into the resinous structure by adding dihydrogen ammonium phosphate in 7,5M HNO 3 . The reactants maintened at 60 0 C for a period of four hours has been found to be the optimum condition for a maximum yield of this compound (anionic resin-ammonium molybdophosphate = R-AMP). The tests performed for characterizing this compound are: molybdenum-phosphorus ratio determination, electronic absorption spectra, infra-red absorption spectra, reflection microscopy observations, electron probe micro-analysis and X-ray powder patterns. The analysis confirmed the presence of the ammonium molybdophosphate in the resinous structure, permitting, thereby, its use as a cation exchanger. R-AMP showed a capacity of 0,48mE/g of dry material. The cesium retention studies were made using columns charged with R-AMP compound. The behavior of polivalent fission products was studied. The R-AMP column was applied to separate cesium from irradiated uranium solutions [pt

  2. Influence of the environmental factors on the intensity of the oxygen, ammonium, and phosphate metabolism in the agar-containing seaweed Ahnfeltia tobuchiensis (Ahnfeltiales, Rhodophyta)

    Science.gov (United States)

    Cherbadgy, I. I.; Sabitova, L. I.

    2011-02-01

    A complex study of the influence of various environmental factors on the rate of the oxygen (MO 2), ammonium (MNH 4), and phosphate (MPO 4) metabolism in Ahnfeltia tobuchiensis has been carried out in situ in the Izmena Bay of Kunashir Island. The following environmental factors have been included into the investigation: the photosynthetically active radiation (PAR); the ammonium (NH4); the phosphate (PO4); and the tissue content of carbon (C), nitrogen (N), phosphorus (P), and chlorophyll a (Chl). The population of agar-containing seaweed A. tobuchiensis forms a layer with a thickness up to 0.5 m, which occupies about 23.3 km2; the population's biomass is equal to 125000 tons. The quantitative assessment of the organic matter production and nutrient consumption during the oxygen metabolism (MO 2) has been carried out for the whole population. It has been shown that the daily rate depends on the PAR intensity, the seawater concentrations of PO4 and NH4, and the tissue content of N and P ( r 2 = 0.78, p < 0.001). The daily NH4 consumption averages 0.21 μmol/(gDW h) and depends on the NH4 and O2 concentrations in the seawater and on the C and Chl a content in the algal tissues ( r 2 = 0.64, p < 0.001). The daily PO4 consumption averages 0.01 μmol/(gDW h) and depends on the NH4 concentration in the seawater and on the P content in the algal tissues ( r 2 = 0.40, p < 0.001).

  3. From dihydrated iron(III) phosphate to monohydrated ammonium-iron(II) phosphate: Solvothermal reaction mediated by acetone-urea mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Alfonso, Belen F., E-mail: mbafernandez@uniovi.es [Departamento de Fisica, Universidad de Oviedo, Calvo Sotelo, s/n 33007 Oviedo (Spain); Trobajo, Camino [Departamento de Quimica Organica e Inorganica, Universidad de Oviedo-CINN, Julian Claveria 8, 33006 Oviedo (Spain); Pique, Carmen [Departamento de Fisica, Universidad de Oviedo, Calvo Sotelo, s/n 33007 Oviedo (Spain); Garcia, Jose R. [Departamento de Quimica Organica e Inorganica, Universidad de Oviedo-CINN, Julian Claveria 8, 33006 Oviedo (Spain); Blanco, Jesus A. [Departamento de Fisica, Universidad de Oviedo, Calvo Sotelo, s/n 33007 Oviedo (Spain)

    2012-12-15

    By reaction between synthetic phosphosiderite FePO{sub 4}{center_dot}2H{sub 2}O, urea (NH{sub 2}){sub 2}CO, and acetone (CH{sub 3}){sub 2}CO, we report a novel solvothermal synthesis of polycrystalline NH{sub 4}FePO{sub 4}{center_dot}H{sub 2}O. The preparation of other two individual phases, NH{sub 4}Fe{sub 2}(OH)(PO{sub 4}){sub 2}{center_dot}2H{sub 2}O and NH{sub 4}Fe{sub 2}(PO{sub 4}){sub 2}, is also described. The obtained product is a function of the reaction time and the N/P molar ratio in the reagent mixture, and the existence of structural memory in the dissolution-precipitation processes is discussed. Below 25 K, NH{sub 4}FePO{sub 4}{center_dot}H{sub 2}O behaves magnetically in a complex way, because both ferromagnetic and antiferromagnetic signals are superimposed, suggesting the existence of a canting of iron(II) magnetic moments. - Graphical abstract: Solvothermal synthesis of polycrystalline NH{sub 4}FePO{sub 4}{center_dot}H{sub 2}O is presented. The preparation of other two individual phases, NH{sub 4}Fe{sub 2}(OH)(PO{sub 4}){sub 2}{center_dot}2H{sub 2}O and NH{sub 4}Fe{sub 2}(PO{sub 4}){sub 2} as a function of the N/P molar ratio in the reagent mixture and the reaction time, is also described. Highlights: Black-Right-Pointing-Pointer Solvothermal synthesis of NH{sub 4}FePO{sub 4}{center_dot}H{sub 2}O from an Fe(III) phosphate: reduction process. Black-Right-Pointing-Pointer Formation of two intermediate metastable phases: phase diagram. Black-Right-Pointing-Pointer Thermal decomposition in two steps: mass loss of both water and ammonia. Black-Right-Pointing-Pointer Magnetic behaviour: AF+constant spontaneous magnetization.

  4. Adsorption of ammonium and phosphate by feather protein based semi-interpenetrating polymer networks hydrogel as a controlled-release fertilizer.

    Science.gov (United States)

    Su, Yuan; Liu, Jia; Yue, Qinyan; Li, Qian; Gao, Baoyu

    2014-01-01

    A new feather protein-grafted poly(potassium acrylate)/polyvinyl alcohol (FP-g-PKA/PVA) semi-interpenetrating polymer networks (semi-IPNs) hydrogel was produced through graft copolymerization with FP as a basic macromolecular skeletal material, acrylic acid as a monomer and PVA as a semi-IPNs polymer. The adsorption of ammonium and phosphate ions from aqueous solution using the new hydrogel as N and P controlled-release fertilizer with water-retention capacity was studied. The effects of pH value, concentration, contact time and ion strength on NH4+ and PO3-4 removal by FP-g-PKA/PVA semi-IPNs hydrogel were investigated using batch adsorption experiments. The results indicated that the hydrogel had high adsorption capacities and fast adsorption rates for NH4+ and PO3-4 in wide pH levels ranging from 4.0 to 9.0. Kinetic analysis presented that both NH4+ and PO3-4 removal were closely fitted with the pseudo-second-order model. Furthermore, the adsorption isotherms of hydrogel were best represented by the Freundlich model. The adsorption-desorption experimental results showed the sustainable stability of FP-g-PKA/PVA semi-IPNs hydrogel for NH4+ and PO3-4 removal. Overall, FP-g-PKA/PVA could be considered as an efficient material for the removal and recovery of nitrogen and phosphorus with the agronomic reuse as a fertilizer.

  5. Efficiency of ammonium nitrate phosphates of varying water-soluble phosphorous content for wheat and succeeding maize crop on different soil types

    International Nuclear Information System (INIS)

    Chapke, V.G.; Bhujbal, B.M.; Mistry, K.B.

    1988-01-01

    Efficiency of 32 P labelled ammonium nitrate phosphate (ANP) containding 30, 50 and 90 per cent of water-soluble phosphorus (WSP) vis-a-vis that of entirely water soluble monoammonium orthophosphate (MAP) for wheat and succeeding maize crop on deep black (vertisol), calcareous black (vertisol), alluvial-Tarai (mollisol) and grey brown alluvial (aridisol) soils was examined in greenhouse experiments. Data on wheat indicated that ANP (50 per cent WSP) was, in general, equally efficient to MAP and ANP (90 per cent WSP) in terms of drymatter yield and total uptake of phosphorus in all soils examined, however, the per cent utilization of applied fertilizer was significantly higher for MAP and ANP (90 per cent WSP) than those for ANP (50 per cent WSP) in all soils. In general, ANP (30 per cent WSP) was significantly inferior to MAP and ANP (90 per cent WSP) in all soils. Data on the succeeding maize crop grown to flowering indicated that residual value of ANP (30 per cent WSP) was equal to that of MAP and ANP (90 per cent WSP) in terms of drymatter yield and phosphorus uptake by the four soils examined. Complementary incubation studies conducted upto 60 days on the above four soils at field capacity moisture status indicated highest 0.5 M NaHCO 3 (pH 8.5) extractable phosphorus levels in MAP treatments followed by ANP (50 per cent WSP) and least in ANP (30 per cent WSP) treatments. (author). 4 tables, 4 figures, 19 refs

  6. Ferrous ammonium phosphate (FeNH₄PO₄) as a new food fortificant: iron bioavailability compared to ferrous sulfate and ferric pyrophosphate from an instant milk drink.

    Science.gov (United States)

    Walczyk, Thomas; Kastenmayer, Peter; Storcksdieck Genannt Bonsmann, Stefan; Zeder, Christophe; Grathwohl, Dominik; Hurrell, Richard F

    2013-06-01

    The main purpose of this study was to establish bioavailability data in humans for the new (Fe) fortification compound ferrous ammonium phosphate (FAP), which was specially developed for fortification of difficult-to-fortify foods where soluble Fe compounds cannot be used due to their negative impact on product stability. A double-blind, randomized clinical trial with cross-over design was conducted to obtain bioavailability data for FAP in humans. In this trial, Fe absorption from FAP-fortified full-cream milk powder was compared to that from ferric pyrophosphate (FPP) and ferrous sulfate. Fe absorption was determined in 38 young women using the erythrocyte incorporation dual stable isotope technique (⁵⁷Fe, ⁵⁸Fe). Geometric mean Fe absorption from ferrous sulfate, FAP and FPP was 10.4, 7.4 and 3.3 %, respectively. Fe from FAP was significantly better absorbed from milk than Fe from FPP (p soluble reference compound (p = 0.0002). Absorption ratios of FAP and FPP relative to ferrous sulfate as a measure of relative bioavailability were 0.71 and 0.32, respectively. The results of the present studies show that replacing FPP with FAP in full-cream milk could significantly improve iron bioavailability.

  7. Effects of soil phosphorus status on environmental risk assessment of glyphosate and glufosinate-ammonium.

    Science.gov (United States)

    Laitinen, Pirkko; Siimes, Katri; Rämö, Sari; Jauhiainen, Lauri; Eronen, Liisa; Oinonen, Seija; Hartikainen, Helinä

    2008-01-01

    The increased use of herbicides poses a risk to the aquatic environment. Easy and economical methods are needed to identify the fields where specific environment protection measures are needed. Phosphorus (P) and organophosphorus herbicides compete for the same adsorption sites in soil. In this study the relationship between P obtained in routine Finnish agronomic tests (acid ammonium acetate [P(AC)]) and adsorption of glyphosate and glufosinate-ammonium was investigated to determine whether P(AC) values could be used in the risk assessment. The adsorption of glyphosate ((N-(phosphonomethyl)glycine) and glufosinate-ammonium (2-amino-4-(hydroxymethylphosphinyl)butanoic acid) was studied in a clay and a sandy loam soil enriched with increasing amounts of P added as potassium dihydrogen phosphate. Desorption was also determined for some P-enriched soil samples. The adsorption of both herbicides diminished with increasing P(AC) value. The correlations between Freundlich adsorption coefficients obtained in the adsorption tests and P(AC) were nonlinear but significant (r > 0.98) in both soils. The exponential models of the relationship between soil P(AC) values and glyphosate adsorption were found to fit well to an independent Finnish soil data set (P glufosinate-ammonium). The desorption results showed that glufosinate-ammonium sorption is not inversely related to soil P status, and the high correlation coefficients obtained in the test of the model were thus artifacts caused by an abnormal concentration of exchangeable potassium in soil. The solved equations are a useful tool in assessing the leaching risks of glyphosate, but their use for glufosinate-ammonium is questionable.

  8. 2-Ureido-1,3-thiazol-3-ium dihydrogen phosphate

    Directory of Open Access Journals (Sweden)

    Kateryna Gubina

    2011-07-01

    Full Text Available The title compound, C4H6N3OS+·H2PO4−, (I, was obtained as a result of hydrolysis of [(1,3-thiazol-2-ylaminocarbonyl]phosphoramidic acid, (II, in water. X-ray analysis has shown that the N—P bond in (II breaks, leading to the formation of the substituted carbamide (I. This compound exists as an internal salt. The unit cell consists of a urea cation and an anion of H2PO4−. Protonation of the N atom of the heterocyclic ring was confirmed by the location of the H atom in a difference Fourier map. The molecules of substituted urea are connected by O...O hydrogen bonds into unlimited planes. In turn, those planes are connected to each other via N—H...O hydrogen bonds with molecules of phosphoric acid, forming a three-dimensional polymer.

  9. Dihydrogen phosphate-water tape and layers vs dihydrogen phosphate layers tuned by hydrophobic isomeric pyridine-diamine functionalized molecules

    Science.gov (United States)

    Huang, Jing; Liu, Tong-Peng; Huo, Li-Hua; Deng, Zhao-Peng; Gao, Shan

    2017-01-01

    Assembly of six isomeric pyridine-diamine-based molecules, N,N‧-bis(pyridin-4-ylmethyl)ethane-1,2-diamine (M1), N,N‧-bis(pyridin-3-ylmethyl)ethane-1,2-diamine (M2), N,N‧-bis(pyridin-2-ylmethyl)ethane-1,2-diamine (M3), N,N‧-bis(pyridin-4-ylmethyl)propane-1,3-diamine (M4), N,N‧-bis(pyridin-3-ylmethyl)propane-1,2-diamine (M5), and N,N‧-bis(pyridin-2-ylmethyl)propane-1,3-diamine (M6), with phosphoric acid (H3PO4) in different ratio (1:2 and 1:4), leads to the formation of nine salts, H2M12+·2H2PO4-·4H2O (1), H2M22+·2H2PO4-·2H2O (2), H2M32+·2H2PO4-·2H2O (3), H4M14+·4H2PO4- (4), H4M24+·4H2PO4- (5), H4M34+·4H2PO4- (6), H2M42+·2H2PO4-·3H2O (7), 2H2M52+·4H2PO4-·2H3PO4 (8), and H2M62+·2H2PO4- (9), which have been characterized by elemental analysis, IR, TG, PL, powder and single-crystal X-ray diffraction. Structural analyses indicate that hydrogen-bonding patterns of H2PO4- anions, conformation of protonated cations can effectively influence the supramolecular architectures through diverse non-covalent interactions. Hydrous salts 1-3 and 7 present 2D and 3D host-guest supramolecular networks, in which the connection of H2PO4- anions and water molecules generates diverse tape and layer motifs. H2PO4- anions in anhydrous salts 4-6 interconnect with each other through hydrogen bonds to form two types of layers, which are joined by discrete H4M4+ cations into 3D inorganic-organic hybrid supramolecular networks. Salts 8-9 also present 2D and 3D host-guest supramolecular networks where the interconnection of H2PO4- anions and its combination with H3PO4 molecules leads to diverse layers. Luminescent analyses indicate that salts 1-9 exhibit violet and blue emission maximum in the range of 390-467 nm at room temperature.

  10. Use of ASP for Removal of Fluorine and Ammonium Ions

    International Nuclear Information System (INIS)

    Martin HB, A; Las, T

    1998-01-01

    The purified zeolites from Bayah, Lampung dan Tasik have been modified into microporous alumino-silico phosphate (ASP) which could be used as anion and cation exchangers. ASP has been prepared by mixing purified zeolites and ammonium dihydrogen phosphate in weight ratios of 1 :1, 1 :5 and 5:1. The materials have been characterized by XRF, XRD and TG. The ion-exchange experiments have been performed by batch method for various concentrations of 0.01, 0.04, 0.08, 0.2 and O,4 NF and NH 4 ion. Column experiment has been performed for: 500 ppm of ion F ( 0,026 N) and 100 ppm (0.0055 N) of ion NH 4 concentrations respectively, fed into 1 cm diameter column containing 3 g pure ion exchangers. From batch experiment the fluorine sorption increases following the increase the concentration and F could be adsorbed up to about 1.09 -9.17 eq/kg for in the range of concentration 0.01 - 0.08 N. For higher fluorine concentration, the fluorine sorption tends to fluctuate. The ammonium sorption experiments obtain similar results for purified zeolites and ASP. The ion could be absorbed up to about 1.09 - 14.24 eq/kg. In column experiment, 1 g ASP could absorb fluorine up to about 278,48 - 334,19 BV ( 900-1300 ml) at 50% BT, and absorb NH 4 about 219.64 - 297.17 BV (850 -1150 ml) separately. These result shows that the ASP might be a potential material to be used for removal of ion F and NH 4 from the waste generayed in the fuel element fabrication

  11. Overexpression, crystallization and preliminary X-ray crystallographic analysis of erythronate-4-phosphate dehydrogenase from Pseudomonas aeruginosa

    Energy Technology Data Exchange (ETDEWEB)

    Ha, Jun Yong; Lee, Ji Hyun; Kim, Kyoung Hoon; Kim, Do Jin; Lee, Hyung Ho; Kim, Hye-Kyung; Yoon, Hye-Jin; Suh, Se Won, E-mail: sewonsuh@snu.ac.kr [Department of Chemistry, College of Natural Sciences, Seoul National University, Seoul 151-742 (Korea, Republic of)

    2006-02-01

    Erythronate-4-phosphate dehydrogenase from P. aeruginosa was crystallized and X-ray diffraction data were collected to 2.20 Å resolution. The enzyme erythronate-4-phosphate dehydrogenase catalyses the conversion of erythronate-4-phosphate to 3-hydroxy-4-phospho-hydroxy-α-ketobutyrate. It belongs to the d-isomer-specific 2-hydroxyacid dehydrogenase family. It is essential for de novo biosynthesis of vitamin B{sub 6} (pyridoxine). Erythronate-4-phosphate dehydrogenase from Pseudomonas aeruginosa, a homodimeric enzyme consisting of two identical 380-residue subunits, has been overexpressed in Escherichia coli with a C-terminal purification tag and crystallized at 297 K using 0.7 M ammonium dihydrogen phosphate, 0.4 M ammonium tartrate, 0.1 M sodium citrate pH 5.6 and 10 mM cupric chloride. X-ray diffraction data were collected to 2.20 Å from a crystal grown in the presence of NADH. The crystals belong to the orthorhombic space group P2{sub 1}2{sub 1}2{sub 1}, with unit-cell parameters a = 84.77, b = 101.28, c = 142.58 Å. A dimeric molecule is present in the asymmetric unit, giving a crystal volume per protein weight (V{sub M}) of 3.64 Å{sup 3} Da{sup −1} and a solvent content of 66%.

  12. Overexpression, crystallization and preliminary X-ray crystallographic analysis of erythronate-4-phosphate dehydrogenase from Pseudomonas aeruginosa

    International Nuclear Information System (INIS)

    Ha, Jun Yong; Lee, Ji Hyun; Kim, Kyoung Hoon; Kim, Do Jin; Lee, Hyung Ho; Kim, Hye-Kyung; Yoon, Hye-Jin; Suh, Se Won

    2006-01-01

    Erythronate-4-phosphate dehydrogenase from P. aeruginosa was crystallized and X-ray diffraction data were collected to 2.20 Å resolution. The enzyme erythronate-4-phosphate dehydrogenase catalyses the conversion of erythronate-4-phosphate to 3-hydroxy-4-phospho-hydroxy-α-ketobutyrate. It belongs to the d-isomer-specific 2-hydroxyacid dehydrogenase family. It is essential for de novo biosynthesis of vitamin B 6 (pyridoxine). Erythronate-4-phosphate dehydrogenase from Pseudomonas aeruginosa, a homodimeric enzyme consisting of two identical 380-residue subunits, has been overexpressed in Escherichia coli with a C-terminal purification tag and crystallized at 297 K using 0.7 M ammonium dihydrogen phosphate, 0.4 M ammonium tartrate, 0.1 M sodium citrate pH 5.6 and 10 mM cupric chloride. X-ray diffraction data were collected to 2.20 Å from a crystal grown in the presence of NADH. The crystals belong to the orthorhombic space group P2 1 2 1 2 1 , with unit-cell parameters a = 84.77, b = 101.28, c = 142.58 Å. A dimeric molecule is present in the asymmetric unit, giving a crystal volume per protein weight (V M ) of 3.64 Å 3 Da −1 and a solvent content of 66%

  13. Effect of Poly(Vinyl Alcohol) Addition on the Properties of Hydrothermal Derived Calcium Phosphate Cement for Bone Filling Materials

    Science.gov (United States)

    Razali, N. N.; Sopyan, I.; Mel, M.; Salleh, H. M.; Rahman, M. M.; Singh, R.

    2017-06-01

    The effect of addition of poly(vinyl alcohol) on hydrothermal derived calcium phosphate cement has been studied. The precursors used to prepare the cement were calcium oxide (CaO) and ammonium dihydrogen phosphate (NH4H2PO4); the reaction was conducted in water at 80-100°C. To improve properties of CPC, poly(vinyl alcohol) (PVA) of 1wt% and 2wt% was added to the liquid phase of CPC and the results were compared to CPC without PVA addition. The addition of PVA was proved to bring remarkable effects on cohesion, setting time and mechanical strength of CPC which make it suitable physically for injectable bone filler applications.

  14. Infrared and Raman Spectra of Magnesium Ammonium Phosphate Hexahydrate (Struvite) and its Isomorphous Analogues. VIII. Spectra of Protiated and Partially Deuterated Magnesium Rubidium Phosphate Hexahydrate and Magnesium Thallium Phosphate Hexahydrate.

    Science.gov (United States)

    Soptrajanov, Bojan; Cahil, Adnan; Najdoski, Metodija; Koleva, Violeta; Stefov, Viktor

    2011-09-01

    The infrared and Raman spectra of magnesium rubidium phosphate hexahydrate MgRbPO4 • 6H2O and magnesium thallium phosphate hexahydrate, MgTlPO4 • 6H2O were recorded at room temperature (RT) and the boiling temperature of liquid nitrogen (LNT). To facilitate their analysis, also recorded were the spectra of partially deuterated analogues with varying content of deuterium. The effects of deuteration and those of lowering the temperature were the basis of the conclusions drawn regarding the origin of the observed bands which were assigned to vibrations which are predominantly localized in the water molecules (four crystallographically different types of such molecules exist in the structures) and those with PO43- character. It was concluded that in some cases coupling of phosphate and water vibrations is likely to take place. The appearance of the infrared spectra in the O-H stretching regions of the infrared spectra is explained as being the result of an extensive overlap of bands due to components of the fundamental stretching modes of the H2O units with a possible participation of bands due to second-order transitions. A broad band reminiscent of the B band of the well-known ABC trio characteristic of spectra of substances containing strong hydrogen bonds in their structure was found around 2400 cm-1 in the infrared spectra of the two studied compounds.

  15. Overexpression, crystallization and preliminary X-­ray crystallographic analysis of erythronate-4-phosphate dehydrogenase from Pseudomonas aeruginosa

    Science.gov (United States)

    Ha, Jun Yong; Lee, Ji Hyun; Kim, Kyoung Hoon; Kim, Do Jin; Lee, Hyung Ho; Kim, Hye-Kyung; Yoon, Hye-Jin; Suh, Se Won

    2006-01-01

    The enzyme erythronate-4-phosphate dehydrogenase catalyses the conversion of erythronate-4-phosphate to 3-hydroxy-4-phospho-hydroxy-α-ketobutyrate. It belongs to the d-isomer-specific 2-hydroxyacid dehydrogenase family. It is essential for de novo biosynthesis of vitamin B6 (pyridoxine). Erythronate-4-­phosphate dehydrogenase from Pseudomonas aeruginosa, a homodimeric enzyme consisting of two identical 380-residue subunits, has been overexpressed in Escherichia coli with a C-terminal purification tag and crystallized at 297 K using 0.7 M ammonium dihydrogen phosphate, 0.4 M ammonium tartrate, 0.1 M sodium citrate pH 5.6 and 10 mM cupric chloride. X-ray diffraction data were collected to 2.20 Å from a crystal grown in the presence of NADH. The crystals belong to the orthorhombic space group P212121, with unit-cell parameters a = 84.77, b = 101.28, c = 142.58 Å. A dimeric molecule is present in the asymmetric unit, giving a crystal volume per protein weight (V M) of 3.64 Å3 Da−1 and a solvent content of 66%. PMID:16511285

  16. Overexpression, crystallization and preliminary X-ray crystallographic analysis of erythronate-4-phosphate dehydrogenase from Pseudomonas aeruginosa.

    Science.gov (United States)

    Ha, Jun Yong; Lee, Ji Hyun; Kim, Kyoung Hoon; Kim, Do Jin; Lee, Hyung Ho; Kim, Hye-Kyung; Yoon, Hye-Jin; Suh, Se Won

    2006-02-01

    The enzyme erythronate-4-phosphate dehydrogenase catalyses the conversion of erythronate-4-phosphate to 3-hydroxy-4-phospho-hydroxy-alpha-ketobutyrate. It belongs to the D-isomer-specific 2-hydroxyacid dehydrogenase family. It is essential for de novo biosynthesis of vitamin B6 (pyridoxine). Erythronate-4-phosphate dehydrogenase from Pseudomonas aeruginosa, a homodimeric enzyme consisting of two identical 380-residue subunits, has been overexpressed in Escherichia coli with a C-terminal purification tag and crystallized at 297 K using 0.7 M ammonium dihydrogen phosphate, 0.4 M ammonium tartrate, 0.1 M sodium citrate pH 5.6 and 10 mM cupric chloride. X-ray diffraction data were collected to 2.20 A from a crystal grown in the presence of NADH. The crystals belong to the orthorhombic space group P2(1)2(1)2(1), with unit-cell parameters a = 84.77, b = 101.28, c = 142.58 A. A dimeric molecule is present in the asymmetric unit, giving a crystal volume per protein weight (VM) of 3.64 A3 Da(-1) and a solvent content of 66%.

  17. Use of combined ion exchangers on the basis of KU-23 and KM-2p cation exchangers for purification of ammonium molybdate and tungstate solutions from phosphate, arsenate, and silicate impurities

    International Nuclear Information System (INIS)

    Blokhin, A.A.; Majorov, D.Yu.; Kopyrin, A.A.; Taushkanov, V.P.

    2002-01-01

    Using the Tracer technique ( 32 P) and elementary analysis, potentiality of using combined ionites on the basis of macroporous cation-exchange resins KU-23 or KM-2p and hydrated zirconium oxide for purification of concentrated solutions of ammonium molybdate and tungstate from phosphate-, arsenate-, and silicate-ions impurities was studied. High selectivity of the combined ionites towards impurity ions was ascertained, which permits reducing the content of impurities by a factor of 50-100 compared with the initial one [ru

  18. Chemistry of dihydrogen complexes containing only phosphorus co ...

    Indian Academy of Sciences (India)

    The trans-[(dppm)2Ru(H)(L)][BF4] complexes (L = phosphine) upon protonation gave the isomerized derivatives, however, further addition of acid resulted in a five-coordinate species, [(dppm)2RuCl]+ presumably via an intermediate phosphine dihydrogen complex. The electronic as well as the steric properties of the ...

  19. Polypyrrole electrodeposited on copper from an aqueous phosphate solution: Corrosion protection properties

    OpenAIRE

    Redondo, Clara; Breslin, Carmel B.

    2007-01-01

    Highly adherent and homogenous polypyrrole films were electrodeposited at copper from a dihydrogen phosphate solution. The polypyrrole films were electrosynthesized in the overoxidized state by cycling the copper electrode from –0.4 to 1.8 V (SCE) in a pyrrole-containing phosphate solution. The growth of the polypyrrole films was facilitated by the initial oxidation of the copper electrode in the phosphate solution to generate a mixed copper–phosphate, copper oxide or hydroxide layer. This la...

  20. The effects of excess calcium on the handling and mechanical properties of hydrothermal derived calcium phosphate bone cement

    Science.gov (United States)

    Razali, N. N.; Sukardi, M. A.; Sopyan, I.; Mel, M.; Salleh, H. M.; Rahman, M. M.

    2018-01-01

    The objective of this study is to determine the effects of excess calcium on the handling and mechanical properties of hydrothermal derived calcium phosphate cement (CPC) for bone filling applications. Hydroxyapatite powder was synthesized via hydrothermal method using calcium oxide, CaO and ammonium dihydrogen phosphate, NH4H2PO4 as the calcium and phosphorus precursors respectively. The effects of calcium excess were evaluated by varying the CaO content at 0, 5 and 15 mole %. The precursors were then refluxed in distilled water at 90-100°C and dried overnight until the calcium phosphate powder was formed. CPC was then produced by mixing the synthesized powder with distilled water at the powder-to-liquid (P/L) ratio of 1.5. The result from the morphological properties of CPC shows the increase in agglomeration and particles size with 5 mole % of calcium excess but decreased with 15 mole % of calcium excess in CPC. This result was in agreement with the compressive strength result where the CPC increased its strength with 5 mole % of calcium excess but reduced with 15 mole % of calcium excess. The excess in calcium precursor also significantly improved the setting time but reduced the injectability of CPC.

  1. Reduced toxicological activity of cigarette smoke by the addition of ammonium magnesium phosphate to the paper of an electrically heated cigarette: smoke chemistry and in vitro cytotoxicity and genotoxicity.

    Science.gov (United States)

    Roemer, E; Stabbert, R; Veltel, D; Müller, B P; Meisgen, T J; Schramke, H; Anskeit, E; Elves, R G; Fournier, J A

    2008-04-01

    The effects of the addition of ammonium magnesium phosphate (AMP) to the paper of an electrically heated cigarette (EHC) prototype on smoke composition and toxicity were quantified and the underlying mechanisms investigated. Smoke from EHC prototypes with and without AMP and from conventional cigarettes, i.e. the University of Kentucky Standard Reference Cigarette 1R4F and eight American-blend market cigarettes, was compared. Endpoints for comparison were smoke chemistry, where toxic constituents were measured, cytotoxic activity, as measured in murine fibroblasts embryo cells by the Neutral Red Uptake Assay, and genotoxic activity, as measured in bacteria by the Salmonella Reverse Mutation Assay and in murine lymphoma cells by the TK Assay. The addition of AMP to the EHC led to a reduction of toxic substances and toxicological activity of approximately 30% compared to the EHC without AMP. Compared to the conventional cigarettes, the EHC with AMP showed reductions of 75-90%. Smoke from the EHCs generated in nitrogen atmospheres supplemented with different concentrations of ammonia and oxygen was assayed for its in vitro cytotoxicity and genotoxicity. The results indicate that the ammonia released by AMP at the heating site of the EHC is responsible for the reductions in cytotoxicity and mutagenicity for the EHC with AMP compared with the EHC without AMP. Thus, while the EHC approach distinctly reduces toxic smoke constituents compared to conventional cigarettes, the use of AMP in the paper of an EHC leads to further distinct reductions. In the study presented here, in vitro assays were used as quantitative tools to investigate toxicity-related mechanisms.

  2. Heterolytic dissociative adsorption state of dihydrogen favored by interfacial defects

    Science.gov (United States)

    Song, Zhenjun; Hu, Hanshi; Xu, Hu; Li, Yong; Cheng, Peng; Zhao, Bin

    2018-03-01

    The atomic-scale insight into dihydrogen on MgO(001) surface deposited on molybdenum substrate with interfacial defects was investigated in detail by employing density functional methods Here we report novel dissociative adsorption behaviors of single hydrogen molecule on the usually inert oxide surfaces, with consideration of two types of dissociation schemes. The heterolytic dissociation state -Mg(H)-O(H)- of dihydrogen is impossible to obtain on neighboring O-Mg sites of perfect bulk MgO(001) terraces. Unusually, the hydrogen molecule can form heterolytic fragmentation states on metal supported MgO(001) films with very low activation barrier (0.398 eV), and the heterolytic dissociation state is much more favorable than homolytic dissociation state both energetically and kinetically in all cases. Electronic properties and bonding attribution of adsorbates and the oxide-metal hybrid structure are revealed by analyzing density of states, differential charge densities, orbital interaction and electron localization function. The characteristic changes to the property and activity of magnesia (001) can have potential application in catalytic reactions.

  3. EPR and optical absorption studies of Cu{sup 2+} doped L-histidinium dihydrogen phosphate–phosphoric acid single crystal

    Energy Technology Data Exchange (ETDEWEB)

    Prabakaran, R.; Sheela, K. Juliet; Rosy, S. Margret [Department of Physics, Gandhigram Rural Institute—Deemed University, Gandhigram, Dindigul-624302, Tamilnadu (India); Radha Krishnan, S.; Shanmugam, V.M. [CSIR-Central Electrochemical Research Institute, Karaikudi-630006, Tamilnadu (India); Subramanian, P., E-mail: psmanian_gri@yahoo.com [Department of Physics, Gandhigram Rural Institute—Deemed University, Gandhigram, Dindigul-624302, Tamilnadu (India)

    2014-02-01

    The EPR spectra of Cu{sup 2+} in L-histidinium dihydrogen phosphate phosphoric acid at room temperature reveal the presence of two magnetically inequivalent Cu{sup 2+} sites in the lattice. The principal values of the g- and A-tensors indicate existence of rhombic symmetry around the Cu{sup 2+} ion. From the direction cosines of the principal values of the g- and A-tensors, the locations of Cu{sup 2+} in the lattice have been identified as substitutional sites. Optical absorption study shows four bands confirm the rhombic symmetry. Photoluminescence study also confirms the rhombic symmetry around the ions.

  4. Hydrogen and dihydrogen bonding of transition metal hydrides

    International Nuclear Information System (INIS)

    Jacobsen, Heiko

    2008-01-01

    Intermolecular interactions between a prototypical transition metal hydride WH(CO) 2 NO(PH 3 ) 2 and a small proton donor H 2 O have been studied using DFT methodology. The hydride, nitrosyl and carbonyl ligand have been considered as site of protonation. Further, DFT-D calculations in which empirical corrections for the dispersion energy are included, have been carried out. A variety of pure and hybrid density functionals (BP86, PW91, PBE, BLYP, OLYP, B3LYP, B1PW91, PBE0, X3LYP) have been considered, and our calculations indicate the PBE functional and its hybrid variation are well suited for the calculation of transition metal hydride hydrogen and dihydrogen bonding. Dispersive interactions make up for a sizeable portion of the intermolecular interaction, and amount to 20-30% of the bond energy and to 30-40% of the bond enthalpy. An energy decomposition analysis reveals that the H...H bond of transition metal hydrides contains both covalent and electrostatic contributions

  5. Hydrogen and dihydrogen bonding of transition metal hydrides

    Science.gov (United States)

    Jacobsen, Heiko

    2008-04-01

    Intermolecular interactions between a prototypical transition metal hydride WH(CO) 2NO(PH 3) 2 and a small proton donor H 2O have been studied using DFT methodology. The hydride, nitrosyl and carbonyl ligand have been considered as site of protonation. Further, DFT-D calculations in which empirical corrections for the dispersion energy are included, have been carried out. A variety of pure and hybrid density functionals (BP86, PW91, PBE, BLYP, OLYP, B3LYP, B1PW91, PBE0, X3LYP) have been considered, and our calculations indicate the PBE functional and its hybrid variation are well suited for the calculation of transition metal hydride hydrogen and dihydrogen bonding. Dispersive interactions make up for a sizeable portion of the intermolecular interaction, and amount to 20-30% of the bond energy and to 30-40% of the bond enthalpy. An energy decomposition analysis reveals that the H⋯H bond of transition metal hydrides contains both covalent and electrostatic contributions.

  6. Hydrogen and dihydrogen bonding of transition metal hydrides

    Energy Technology Data Exchange (ETDEWEB)

    Jacobsen, Heiko [KemKom, Libellenweg 2, 25917 Leck, Nordfriesland (Germany)], E-mail: jacobsen@kemkom.com

    2008-04-03

    Intermolecular interactions between a prototypical transition metal hydride WH(CO){sub 2}NO(PH{sub 3}){sub 2} and a small proton donor H{sub 2}O have been studied using DFT methodology. The hydride, nitrosyl and carbonyl ligand have been considered as site of protonation. Further, DFT-D calculations in which empirical corrections for the dispersion energy are included, have been carried out. A variety of pure and hybrid density functionals (BP86, PW91, PBE, BLYP, OLYP, B3LYP, B1PW91, PBE0, X3LYP) have been considered, and our calculations indicate the PBE functional and its hybrid variation are well suited for the calculation of transition metal hydride hydrogen and dihydrogen bonding. Dispersive interactions make up for a sizeable portion of the intermolecular interaction, and amount to 20-30% of the bond energy and to 30-40% of the bond enthalpy. An energy decomposition analysis reveals that the H...H bond of transition metal hydrides contains both covalent and electrostatic contributions.

  7. Systems of amonium polyborates - monoammonium phosphate -water at 25 deg C

    International Nuclear Information System (INIS)

    Skvortsov, V.G.; Sadetdinov, Sh.V.; Polenov, A.D.; Mikhajlov, V.I.

    1992-01-01

    It is established by solubility and refractometry methods at 25 deg C that systems of ammonium tetraborate (pentaborate) monoammonium phosphate-water refer to sumple eutonic type. The ammonium borates and monoammoniumphosphate exert salting effect over each other. It is found that phosphate borate compositions on the basis of ammonium salts are characterized by lower inhibitor properties as compared to sodium salts

  8. Elevated ammonium levels

    DEFF Research Database (Denmark)

    Søgaard, Rikke; Novak, Ivana; MacAulay, Nanna

    2012-01-01

    was not enhanced. The ammonium-induced stimulation of EAAT3 increased with increasing extracellular pH, suggesting that the gaseous form NH(3) mediates the effect. An ammonium-induced intracellular alkalinization was excluded as the cause of the enhanced EAAT3 activity because 1) ammonium acidified the oocyte...

  9. Ammonium nitrate explosion hazards

    Directory of Open Access Journals (Sweden)

    Negovanović Milanka

    2015-01-01

    Full Text Available Ammonium nitrate (AN primarily is used as a fertilizer but it is also very important compound in the production of industrial explosives. The application of ammonium nitrate in the production of industrial explosives was related with the early era of Nobel dynamite and widely increased with the appearance of blasting agents such as ANFO and Slurry, in the middle of the last Century. Throughout the world millions of tons of ammonium nitrate are produced annually and handled without incident. Although ammonium nitrate generally is used safely, accidental explosions involving AN have high impact resulting in loss of lives and destruction of property. The paper presents the basic properties of ammonium nitrate as well as hazards in handling of ammonium nitrate in order to prevent accidents. Several accidents with explosions of ammonium nitrate resulted in catastrophic consequences are listed in the paper as examples of non-compliance with prescribed procedures.

  10. Fatores de retardamento e coeficientes de dispersão-difusão de fosfato, potássio e amônio em solos de Minas Gerais Retardation factors and dispersion-diffusion coefficients of phosphate, potassium and ammonium in soils of Minas Gerais - Brazil

    Directory of Open Access Journals (Sweden)

    Ermelinda M. M. Oliveira

    2004-12-01

    Full Text Available Através deste estudo objetivou-se comparar os fatores de retardamento (R e os coeficientes de dispersão-difusão (D do fosfato, potássio e amônio, determinados em cinco solos de Minas Gerais (um Neossolo Quartzarênico órtico - RQo; três Latossolos Vermelhos distróficos - LVd1, LVd2 e LVd3; e um Latossolo Vermelho-Amarelo distrófico - LVAd. O experimento foi realizado utilizando-se colunas de percolação, que receberam aplicações de uma das soluções resultantes das oito possíveis combinações de duas concentrações de fosfato, potássio e amônio (15 e 60 mg L-1 de P, 75 e 300 mg L-1 de K e 15 e 60 mg L-1 de N. Valores menores de R para o potássio e o amônio, foram observados, quando comparados com os do fosfato. O R para fosfato foi menor no solo mais arenoso (RQo e maior no mais oxídico (LVd2, enquanto nos Latossolos os maiores valores do R para potássio e amônio estiveram relacionados com o incremento do teor de argila, sem tendência definida quanto á concentração do íon em estudo ou do íon acompanhante. Não se evidenciou relação nítida entre as concentrações de fosfato, potássio e amônio e os D desses íons nos solos estudados.The objective of this study was to compare the retardation factors (R, and dispersion-diffusion coefficients (D of phosphate, potassium and ammonium, determined in five Brazilian soils from Minas Gerais State (Orthic Quartzarenic Neosoil, RQo; three distrophic Red Latosols, LVd1, LVd2 and LVd3; and a distrophic Yellow-Red Latosol, LVAd. The experiment used percolation columns, applying one of the eight possible solutions resulting from the mixture of two phosphate, potassium and ammonium concentrations (15 and 60 mg L-1 P, 75 and 300 mg L-1 K, and 15 and 60 mgL-1 N. Lower values of R were observed for potassium and ammonium compared to phosphate. The value of R for phosphate was the lowest in the most sandy soil (RQo and highest in the most oxidic soil (LVd2. The highest Latosol

  11. Systems of amonium polyborates - monoammonium phosphate -water at 25 deg C. Sistemy poliboraty ammoniya - monoammonijfosfat - voda pri 25 grad S

    Energy Technology Data Exchange (ETDEWEB)

    Skvortsov, V G; Sadetdinov, Sh V; Polenov, A D; Mikhajlov, V I [Chuvashskij Gosudarstvennyj Pedagogicheskij Inst., Cheboksary (Russian Federation)

    1992-11-01

    It is established by solubility and refractometry methods at 25 deg C that systems of ammonium tetraborate (pentaborate) monoammonium phosphate-water refer to sumple eutonic type. The ammonium borates and monoammoniumphosphate exert salting effect over each other. It is found that phosphate borate compositions on the basis of ammonium salts are characterized by lower inhibitor properties as compared to sodium salts.

  12. Interactively Applying the Variational Method to the Dihydrogen Molecule: Exploring Bonding and Antibonding

    Science.gov (United States)

    Cruzeiro, Vinícius Wilian D.; Roitberg, Adrian; Polfer, Nicolas C.

    2016-01-01

    In this work we are going to present how an interactive platform can be used as a powerful tool to allow students to better explore a foundational problem in quantum chemistry: the application of the variational method to the dihydrogen molecule using simple Gaussian trial functions. The theoretical approach for the hydrogen atom is quite…

  13. Structural, spectroscopic and Thermal Studies of Potassium Di-hydrogen Citrate Crystal

    Directory of Open Access Journals (Sweden)

    N.D. Pandya

    2017-04-01

    Full Text Available Potassium dihydrogen citrate (KDC finds wide applications in food products. Pure potassium dihydrogen citrate crystal was grown by slow solvent evaporation technique at room temperature. Grown crystal exhibited needle like morphology. The powder XRD shows triclinic structure symmetry with lattice parameters a=11.820 Å, b=14.970 Å, c=9.442 Å with angles α = 91.60°, β = 93.35°, γ = 110°. The presence of various functional groups of grown crystal was confirmed by using FT-IR spectroscopy. The thermogram indicates the thermal stability of the sample up to 100oC and then decomposes slowly into oxide stage through two stages. The results are discussed here.

  14. Novel Ammonium Metal Borohydrides

    DEFF Research Database (Denmark)

    Grinderslev, Jakob; Jepsen, Lars Haahr; Cerny, Radovan

    Ammonium borohydride, NH4BH4, has a very high gravimetric (ρm = 24.5 wt% H2) and volumetric (157.3 g·H2/L) hydrogen content and releases 18.4 wt% H2 below 170 °C. However, NH4BH4 is metastable at RT and ambient pressure, with a half-life of ~6 h. The decomposition is strongly exothermic; therefore......, it cannot store hydrogen reversibly. Recently, the first ammonium metal borohydride, NH4Ca(BH4)3 was published, which may be considered as substitution of K+ by NH4+ in KCa(BH4)3, due to the similar sizes of NH4+ and K+[1]. This compound successfully stabilizes NH4BH4. In the present work, a series of novel...... halide-free ammonium metal borohydrides is presented, which have the chemical compositions (NH4)xM(BH4)n+x. The ammonium metal borohydrides are synthesized by cryomilling of NH4BH4 – M(BH4)n (M = Li, Na, K, Mg, Sr, Y, Mn, La, Gd) in different ratios. A new range of ammonium metal borohydrides is formed...

  15. Novel Ammonium Metal Borohydrides

    DEFF Research Database (Denmark)

    Grinderslev, Jakob; Jepsen, Lars Haahr; Cerny, Radovan

    , it cannot store hydrogen reversibly. Recently, the first ammonium metal borohydride, NH4Ca(BH4)3 was published, which may be considered as substitution of K+ by NH4+ in KCa(BH4)3, due to the similar sizes of NH4+ and K+[1]. This compound successfully stabilizes NH4BH4. In the present work, a series of novel...... halide-free ammonium metal borohydrides is presented, which have the chemical compositions (NH4)xM(BH4)n+x. The ammonium metal borohydrides are synthesized by cryomilling of NH4BH4 – M(BH4)n (M = Li, Na, K, Mg, Sr, Y, Mn, La, Gd) in different ratios. A new range of ammonium metal borohydrides is formed......, and the crystal structures and thermal decompositions are investigated. Mixtures of NH4BH4 - NaBH4 do not react, while solid solutions, K1-x(NH4)xBH4, are formed for NH4BH4 - KBH4. For the other composites, novel ammonium metal borohydrides are formed. Several of these structures have been solved from high...

  16. Waterproofing Materials for Ammonium Nitrate

    OpenAIRE

    R.S. Damse

    2004-01-01

    This study explores the possibility of overcoming the problem of hygroscopicity of ammonium nitrate by coating the particles with selected waterproofing materials. Gravimetric analysis ofthe samples of ammonium nitrate coated with eight different waterproofing materials, vis-a-vis, uncoated ammonium nitrate, were conducted at different relative humidity and exposuretime. The results indicate that mineral jelly is the promising waterproofing material for ammonium nitrate among the materials te...

  17. Polyethylene flame retarded with expandable graphite and a novel intumescent additive

    CSIR Research Space (South Africa)

    Focke, WW

    2014-07-01

    Full Text Available A novel intumescent additive was synthesized by neutralizing 3,5-diaminobenzoic acid hydrochloride salt with ammonium dihydrogen phosphate. This compound, which melts at 257 C, decomposes concurrently to release carbon dioxide gas. The flame...

  18. Amide Synthesis from Alcohols and Amines by the Extrusion of Dihydrogen

    DEFF Research Database (Denmark)

    Nordstrøm, Lars Ulrik Rubæk; Vogt, Henning; Madsen, R.

    2008-01-01

    An environmentally friendly method for synthesis of amides is presented where a simple ruthenium catalyst mediates the direct coupling between an alcohol and an amine with the liberation of two molecules of dihydrogen. The active catalyst is generated in situ from an easily available ruthenium...... complex, an N-heterocyclic carbene and a phosphine. The reaction allows primary alcohols to be coupled with primary alkyamines to afford the corresponding secondary amides in good yields. The amide formation presumably proceeds through a catalytic cycle where the intermediate aldehyde and hemiaminal...

  19. Spectrophotometric Determination of Nitrate and Phosphate Levels ...

    African Journals Online (AJOL)

    MBI

    2013-04-09

    Apr 9, 2013 ... may help in the growth of algae (Beavington,. 1977). Determination of phosphate ion in drinking water. 50cm3 of water sample was pipetted into a 500cm3 volumetric flask, 5cm3 of Ammonium molybdate solution and 3.0cm3 of ascorbic acid were added with swirling, the mixture was diluted to the mark with ...

  20. Prevention of radioactive contamination in the manufacture of phosphate fertilizers

    International Nuclear Information System (INIS)

    Romero G, E.T.

    1995-01-01

    In this work was studied the separation of uranium from the phosphate rock to decrease the level of radioactivity in the phosphate fertilizers, this prevents the redistribution of uranium in the environment. The uranium leaching conditions from phosphate rock were estimated using alkaline solutions. The changes in the natural phosphate rock after leaching were studied. The amenability to separate the uranium from phosphate rock with ammonium carbonate / bicarbonate solution was determined. The uranium extraction was approximately 40%. The leaching conditions showed high selectivity for uranium without changes in the ore structure. The bulk ore was not dissolved. (Author)

  1. Reversible dihydrogen activation and hydride transfer by a uranium nitride complex

    Energy Technology Data Exchange (ETDEWEB)

    Falcone, Marta; Poon, Lok Nga; Fadaei Tirani, Farzaneh; Mazzanti, Marinella [Institut des Sciences et Ingenierie Chimiques, Ecole Polytechnique Federale de Lausanne (EPFL), Lausanne (Switzerland)

    2018-03-26

    Cleavage of dihydrogen is an important step in the industrial and enzymatic transformation of N{sub 2} into ammonia. The reversible cleavage of dihydrogen was achieved under mild conditions (room temperature and 1 atmosphere of H{sub 2}) by the molecular uranium nitride complex, [Cs{U(OSi(O"tBu)_3)_3}{sub 2}(μ-N)], leading to a rare hydride-imide bridged diuranium(IV) complex, [Cs{U(OSi(O"tBu)_3)_3}{sub 2}(μ-H)(μ-NH)], that slowly releases H{sub 2} under vacuum. This complex is highly reactive and quickly transfers hydride to acetonitrile and carbon dioxide at room temperature, affording the ketimide- and formate-bridged U{sup IV} species [Cs{U(OSi(O"tBu)_3)_3}{sub 2}(μ-NH)(μ-CH{sub 3}CHN)] and [Cs{U(OSi(O"tBu)_3)_3}{sub 2}(μ-HCOO)(μ-NHCOO)]. (copyright 2018 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  2. Crystal structure, vibrational and DFT simulation studies of melaminium dihydrogen phosphite monohydrate

    Science.gov (United States)

    Arjunan, V.; Kalaivani, M.; Marchewka, M. K.; Mohan, S.

    2013-08-01

    The crystal structure investigations of melamine with phosphorous acid, namely melaminium dihydrogenphosphite monohydrate (C3N6H7·H2PO3·H2O) have been investigated by means of single crystal X-ray diffraction method. The title compound crystallizes in monoclinic crystal system, and the space group is P21/c with a = 10.069 Å, b = 21.592 Å, c = 12.409 Å and Z = 12. The vibrational assignments and analysis of melaminium dihydrogen phosphite monohydrate have also been performed by FTIR, FT-Raman and far-infrared spectral studies. The quantum chemical simulations were performed with DFT (B3LYP) method using 6-31G**, cc-pVTZ, and 6-311++G** basis sets to determine the energy, structural, thermodynamic parameters and vibrational frequencies of melaminium dihydrogen phosphite monohydrate. The hydrogen atom from phosphorous acid was transferred to the melamine molecule giving the singly protonated melaminium cation. The ability of ions to form spontaneous three-dimensional structure through weak Osbnd H···O and Nsbnd H···O hydrogen bonds shows notable vibrational effects.

  3. Ammonium on Ceres

    Science.gov (United States)

    Ammannito, E.; De Sanctis, M. C.; Carrorro, F. G.; Ciarniello, M.; Combe, J. P.; De Angelis, S.; Ehlmann, B. L.; Frigeri, A.; Longobardo, A.; Mugnuolo, R.; Marchi, S.; Palomba, E.; Raymond, C. A.; Salatti, M.; Tosi, F.; Zambon, F.; Russell, C. T.

    2017-12-01

    Since January 2015, the surface of Ceres has been studied by the Dawn spacecraft through the measurements from the three instruments on board (1). The VIR imaging spectrometer, sensitive to the spectral range 0.25 -5.0 μm, provided information on the surficial composition of Ceres at resolutions ranging from few kilometers to about one hundred meters (2). Analysis of VIR reflectance data revealed that the average spectrum of Ceres is compatible with a mixture of low-albedo minerals, Mg- phyllosilicates, ammoniated clays, and Mg- carbonates, (3) confirming previous studies based on ground based spectra (4, 5). Mineralogical maps of the surface at about 1 km/px show that the components identified in the average spectrum are present all across the surface with variations in their relative abundance and chemical composition (6, 7). While the ammoniated clays have been already studied (6), the presence nature and distribution of additional ammoniated species has never been investigated in detail, although the spectral analysis of the bright faculae within Occator crater already revealed the potential presence of ammonium salts (8). Since the position and shape of the ammonium absorption in the VIS-NIR region are function of the hosting mineral specie (8), we did an inventory and characterization of the ammonium-rich regions, in order to analyze their spectral properties. In addition to the presence of ammonium, also the identification of the hosting species has implication for the evolution of Ceres. Our study, therefore, is a step forward in understanding of evolutionary pathway of Ceres. References: (1) Russell, C. T. et al., Science, 2016. (2) De Sanctis M.C. et al., Space Science Reviews, 2011. (3) De Sanctis M.C. et al., Nature, 2015. (4) King T. et al. Science, 1992. (5) Rivkin A.S. et al. Icarus, 2006. (6) Ammannito E. et al., Science, 2016. (7) Carrozzo F.G. et al., Science Advances, in revision. (8) De Sanctis et al., Nature, 2016. (9) Berg et al., Icarus

  4. Dihydrogen Phosphate Stabilized Ruthenium(0 Nanoparticles: Efficient Nanocatalyst for The Hydrolysis of Ammonia-Borane at Room Temperature

    Directory of Open Access Journals (Sweden)

    Feyyaz Durap

    2015-07-01

    Full Text Available Intensive efforts have been devoted to the development of new materials for safe and efficient hydrogen storage. Among them, ammonia-borane appears to be a promising candidate due to its high gravimetric hydrogen storage capacity. Ammonia-borane can release hydrogen on hydrolysis in aqueous solution under mild conditions in the presence of a suitable catalyst. Herein, we report the synthesis of ruthenium(0 nanoparticles stabilized by dihydrogenphosphate anions with an average particle size of 2.9 ± 0.9 nm acting as a water-dispersible nanocatalyst in the hydrolysis of ammonia-borane. They provide an initial turnover frequency (TOF value of 80 min−1 in hydrogen generation from the hydrolysis of ammonia-borane at room temperature. Moreover, the high stability of these ruthenium(0 nanoparticles makes them long-lived and reusable nanocatalysts for the hydrolysis of ammonia-borane. They provide 56,800 total turnovers and retain ~80% of their initial activity even at the fifth catalytic run in the hydrolysis of ammonia-borane at room temperature.

  5. Dihydrogen Phosphate Stabilized Ruthenium(0) Nanoparticles: Efficient Nanocatalyst for The Hydrolysis of Ammonia-Borane at Room Temperature

    Science.gov (United States)

    Durap, Feyyaz; Caliskan, Salim; Özkar, Saim; Karakas, Kadir; Zahmakiran, Mehmet

    2015-01-01

    Intensive efforts have been devoted to the development of new materials for safe and efficient hydrogen storage. Among them, ammonia-borane appears to be a promising candidate due to its high gravimetric hydrogen storage capacity. Ammonia-borane can release hydrogen on hydrolysis in aqueous solution under mild conditions in the presence of a suitable catalyst. Herein, we report the synthesis of ruthenium(0) nanoparticles stabilized by dihydrogenphosphate anions with an average particle size of 2.9 ± 0.9 nm acting as a water-dispersible nanocatalyst in the hydrolysis of ammonia-borane. They provide an initial turnover frequency (TOF) value of 80 min−1 in hydrogen generation from the hydrolysis of ammonia-borane at room temperature. Moreover, the high stability of these ruthenium(0) nanoparticles makes them long-lived and reusable nanocatalysts for the hydrolysis of ammonia-borane. They provide 56,800 total turnovers and retain ~80% of their initial activity even at the fifth catalytic run in the hydrolysis of ammonia-borane at room temperature. PMID:28793435

  6. Phosphate glasses, containing nitrogen

    International Nuclear Information System (INIS)

    Lisitsyna, E.A.; Khalilev, V.D.; Koryavin, A.A.; Goncharova, L.N.

    1987-01-01

    Possibilities of nitrogen-containing glass synthesis by the introduction into the charge of ammonium salts, as well as aluminium nitride, are studied. Zinc alumoyttrium phosphate glass (mol. %) Zn(PO 3 ) 2 - 4O, Al(PO 3 ) 3 - 3O, Y(PO 3 ) 3 -3O is suggested as a matrix. It is shown that the effect of amide and imide groups on the properties of the glass is less noticeable than the effect of nitride groups. Direct introduction of nitride constituent was realized using AlN, but aluminium introduction was taken into account so that the oxide was subtracted. The attempt to introduce more than 2.5 mass % of nitrogen into initial matrix by aluminium nitride has failed due to repeated restoration of glass with amorphous phosphorus isolation

  7. Phosphate Salts

    Science.gov (United States)

    ... body. They are involved in cell structure, energy transport and storage, vitamin function, and numerous other processes ... Phosphate-containing foods and beverages include cola, wine, beer, whole grain cereals, nuts, dairy products and some ...

  8. Crystallisation of mixtures of ammonium nitrate, ammonium sulphate and soot

    NARCIS (Netherlands)

    Dougle, P.G.; Veefkind, J.P.; Brink, H.M. ten

    1998-01-01

    Crystallisation of laboratory aerosols of ammonium nitrate and of internal mixtures of this salt with ammonium sulphate were investigated using humidity controlled nephelometry. The aerosol was produced via nebulizing of solutions and then dried to 25% RH, which is a realistic minimum value for

  9. Studies on the Effects of Ammonium Phosphates on the ...

    African Journals Online (AJOL)

    Nigerian Journal of Basic and Applied Science (June, 2012), 20(2): 173-176. ISSN 0794-5698. Studies ... 2Department of Pure and Industrial Chemistry, Bayero University, Kano, Nigeria. 3Department of ... MATERIALS AND METHODS. Poly(vinyl .... Organic Chemistry, 4th ... and Engineering, 2nd edn, Reed Elsevier India.

  10. Magnesium-phosphate-glass cements with ceramic-type properties

    Science.gov (United States)

    Sugama, T.; Kukacka, L.E.

    1982-09-23

    Rapid setting magnesium phosphate (Mg glass) cementitious materials consisting of magnesium phosphate cement paste, polyborax and water-saturated aggregate, exhibits rapid setting and high early strength characteristics. The magnesium glass cement is prepared from a cation-leachable powder and a bivalent metallic ion-accepting liquid such as an aqueous solution of diammonium phosphate and ammonium polyphosphate. The cation-leachable powder includes a mixture of two different magnesium oxide powders processed and sized differently which when mixed with the bivalent metallic ion-accepting liquid provides the magnesium glass cement consisting primarily of magnesium ortho phosphate tetrahydrate, with magnesium hydroxide and magnesium ammonium phosphate hexahydrate also present. The polyborax serves as a set-retarder. The resulting magnesium mono- and polyphosphate cements are particularly suitable for use as a cementing matrix in rapid repair systems for deteriorated concrete structures as well as construction materials and surface coatings for fireproof structures.

  11. Magnesium phosphate glass cements with ceramic-type properties

    Science.gov (United States)

    Sugama, Toshifumi; Kukacka, Lawrence E.

    1984-03-13

    Rapid setting magnesium phosphate (Mg glass) cementitious materials consisting of magnesium phosphate cement paste, polyborax and water-saturated aggregate exhibiting rapid setting and high early strength characteristics. The magnesium glass cement is prepared from a cation-leachable powder and a bivalent metallic ion-accepting liquid such as an aqueous solution of diammonium phosphate and ammonium polyphosphate. The cation-leachable powder includes a mixture of two different magnesium oxide powders processed and sized differently which when mixed with the bivalent metallic ion-accepting liquid provides the magnesium glass cement consisting primarily of magnesium ortho phosphate tetrahydrate, with magnesium hydroxide and magnesium ammonium phosphate hexahydrate also present. The polyborax serves as a set-retarder. The resulting magnesium mono- and polyphosphate cements are particularly suitable for use as a cementing matrix in rapid repair systems for deteriorated concrete structures as well as construction materials and surface coatings for fireproof structures.

  12. Ammonium diphosphitoindate(III

    Directory of Open Access Journals (Sweden)

    Farida Hamchaoui

    2013-04-01

    Full Text Available The crystal structure of the title compound, NH4[In(HPO32], 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(HPO32]− 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(HPO32]− 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.

  13. Early metabolic effects and mechanism of ammonium transport in yeast

    International Nuclear Information System (INIS)

    Pena, A.; Pardo, J.P.; Ramirez, J.

    1987-01-01

    Studies were performed to define the effects and mechanism of NH+4 transport in yeast. The following results were obtained. Glucose was a better facilitator than ethanol-H 2 O 2 for ammonium transport; low concentrations of uncouplers or respiratory inhibitors could inhibit the transport with ethanol as the substrate. With glucose, respiratory inhibitors showed only small inhibitory effects, and only high concentrations of azide or trifluoromethoxy carbonylcyanide phenylhydrazone could inhibit ammonium transport. Ammonium in the free state could be concentrated approximately 200-fold by the cells. Also, the addition of ammonium produced stimulation of both respiration and fermentation; an increased rate of H+ extrusion and an alkalinization of the interior of the cell; a decrease of the membrane potential, as monitored by fluorescent cyanine; an immediate decrease of the levels of ATP and an increase of ADP, which may account for the stimulation of both fermentation and respiration; and an increase of the levels of inorganic phosphate. Ammonium was found to inhibit 86Rb+ transport much less than K+. Also, while K+ produced a competitive type of inhibition, that produced by NH4+ was of the noncompetitive type. From the distribution ratio of ammonium and the pH gradient, an electrochemical potential gradient of around -180 mV was calculated. The results indicate that ammonium is transported in yeast by a mechanism similar to that of monovalent alkaline cations, driven by a membrane potential. The immediate metabolic effects of this cation seem to be due to an increased [H+]ATPase, to which its transport is coupled. However, the carriers seem to be different. The transport system studied in this work was that of low affinity

  14. Ammonium generation during SRAT cycle

    International Nuclear Information System (INIS)

    Hsu, C.W.

    1992-01-01

    During the IDMS noble-metal demonstration runs ammonium nitrate deposition was found in the vessel vent system of the feed preparation area. In the bench-scale experiments of studying the hydrogen generation during the sludge treatment cycle, ammonium ion production was also monitored. It was found that: During a simulation of the DWPF Cold Chemical Runs SRAT cycle no detectable amount of ammonium ions was generated when treating a non-noble-metal containing sludge simulant according to the nitric acid flowsheet. Ammonium ions were generated during the SRAT-SME cycle when treating the noble-metal containing sludge with either formic acid or nitric acid/late-washing PHA. This is due to the reaction between formic acid and nitrate catalyzed by the noble metals in the sludge simulant. Ammonium ion production closely followed the hydrogen evolution from the catalytic decomposition of formic acid. This report summarizes the results of the production of ammonia during the SRAT cycle

  15. Electro-activity of cobalt and nickel complexes for the reduction of protons into di-hydrogen; Electroactivite de complexes de cobalt et nickel pour la reduction des protons en di-hydrogene

    Energy Technology Data Exchange (ETDEWEB)

    Pantani, O.; Anxolabehere-Mallart, E.; Aukauloo, A.; Millet, P. [Paris-11 Univ., Equipe de Chimie Inorganique, UMR 8182, ICMMO, 91 - Orsay (France)

    2007-07-01

    In this study, the results obtained with different cobalt and nickel glyoximes are presented. These complexes have been characterized by various spectroscopies (UV-visible, ESR) and by electrochemistry (cyclic voltametry, spectro-electrochemistry). Their efficiency to electrochemically reduce the protons into dihydrogen in acid medium is discussed. More particularly, studies on solid support are carried out. At last, these complexes are being tested inside PEM electrolysis. (O.M.)

  16. Ammonium nitrogen removal from coking wastewater by chemical precipitation recycle technology.

    Science.gov (United States)

    Zhang, Tao; Ding, Lili; Ren, Hongqiang; Xiong, Xiang

    2009-12-01

    Ammonium nitrogen removal from wastewater has been of considerable concern for several decades. In the present research, we examined chemical precipitation recycle technology (CPRT) for ammonium nitrogen removal from coking wastewater. The pyrolysate resulting from magnesium ammonium phosphate (MAP) pyrogenation in sodium hydroxide (NaOH) solution was recycled for ammonium nitrogen removal from coking wastewater. The objective of this study was to investigate the conditions for MAP pyrogenation and to characterize of MAP pyrolysate for its feasibility in recycling. Furthermore, MAP pyrolysate was characterized by scanning electron microscope (FESEM), transmission electron microscope (TEM), Fourier transform infrared spectroscopy (FTIR) as well as X-ray diffraction (XRD). The MAP pyrolysate could be produced at the optimal condition of a hydroxyl (OH(-)) to ammonium molar ratio of 2:1, a heating temperature of 110 degrees C, and a heating time of 3h. Surface characterization analysis indicated that the main component of the pyrolysate was amorphous magnesium sodium phosphate (MgNaPO(4)). The pyrolysate could be recycled as a magnesium and phosphate source at an optimum pH of 9.5. When the recycle times were increased, the ammonium nitrogen removal ratio gradually decreased if the pyrolysate was used without supplementation. When the recycle times were increased, the ammonium nitrogen removal efficiency was not decreased if the added pyrolysate was supplemented with MgCl(2).6H(2)O plus Na(2)HPO(4).12H(2)O during treatment. A high ammonium nitrogen removal ratio was obtained by using pre-formed MAP as seeding material.

  17. Electro-activity of cobalt and nickel complexes for the reduction of protons into di-hydrogen

    International Nuclear Information System (INIS)

    Pantani, O.; Anxolabehere-Mallart, E.; Aukauloo, A.; Millet, P.

    2007-01-01

    In this study, the results obtained with different cobalt and nickel glyoximes are presented. These complexes have been characterized by various spectroscopies (UV-visible, ESR) and by electrochemistry (cyclic voltametry, spectro-electrochemistry). Their efficiency to electrochemically reduce the protons into dihydrogen in acid medium is discussed. More particularly, studies on solid support are carried out. At last, these complexes are being tested inside PEM electrolysis. (O.M.)

  18. 21 CFR 184.1138 - Ammonium chloride.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ammonium chloride. 184.1138 Section 184.1138 Food... Specific Substances Affirmed as 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...

  19. Diverse roles of hydrogen in rhenium carbonyl chemistry: hydrides, dihydrogen complexes, and a formyl derivative.

    Science.gov (United States)

    Li, Nan; Xie, Yaoming; King, R Bruce; Schaefer, Henry F

    2010-11-04

    Rhenium carbonyl hydride chemistry dates back to the 1959 synthesis of HRe(CO)₅ by Hieber and Braun. The binuclear H₂Re₂(CO)₈ was subsequently synthesized as a stable compound with a central Re₂(μ-H)₂ unit analogous to the B₂(μ-H)₂ unit in diborane. The complete series of HRe(CO)(n) (n = 5, 4, 3) and H₂Re₂(CO)(n) (n = 9, 8, 7, 6) derivatives have now been investigated by density functional theory. In contrast to the corresponding manganese derivatives, all of the triplet rhenium structures are found to lie at relatively high energies compared with the corresponding singlet structures consistent with the higher ligand field splitting of rhenium relative to manganese. The lowest energy HRe(CO)₅ structure is the expected octahedral structure. Low-energy structures for HRe(CO)(n) (n = 4, 3) are singlet structures derived from the octahedral HRe(CO)₅ structure by removal of one or two carbonyl groups. For H₂Re₂(CO)₉ a structure HRe₂(CO)₉(μ-H), with one terminal and one bridging hydrogen atom, lies within 3 kcal/mol of the structure Re₂(CO)₉(η²-H₂), similar to that of Re₂(CO)₁₀. For H₂Re₂(CO)(n) (n = 8, 7, 6) the only low-energy structures are doubly bridged singlet Re₂(μ-H)₂(CO)(n) structures. Higher energy dihydrogen complex structures are also found.

  20. Intercalation of gaseous thiols and sulfides into Ag+ ion-exchanged aluminum dihydrogen triphosphate.

    Science.gov (United States)

    Hayashi, Aki; Saimen, Hiroki; Watanabe, Nobuaki; Kimura, Hitomi; Kobayashi, Ayumi; Nakayama, Hirokazu; Tsuhako, Mitsutomo

    2005-08-02

    Ag(+) ion-exchanged layered aluminum dihydrogen triphosphate (AlP) with the interlayer distance of 0.85 nm was synthesized by the ion-exchange of proton in triphosphate with Ag(+) ion. The amount of exchanged Ag(+) ion depended on the concentration of AgNO(3) aqueous solution. Ag(+) ion-exchanged AlP adsorbed gaseous thiols and sulfides into the interlayer region. The adsorption amounts of thiols were more than those of sulfides, thiols with one mercapto group > thiol with two mercapto groups > sulfides, and depended on the amount of exchanged Ag(+) ion in the interlayer region. The thiols with one mercapto group were intercalated to expand the interlayer distance of Ag(+) ion-exchanged AlP, whereas there was no expansion in the adsorption of sulfide. In the case of thiol with two mercapto groups, there was observed contraction of the interlayer distance through the bridging with Ag(+) ions of the upper and lower sides of the interlayer region.

  1. Synthesis, vibrational and quantum chemical investigations of hydrogen bonded complex betaine dihydrogen selenite

    Science.gov (United States)

    Arjunan, V.; Marchewka, Mariusz K.; Kalaivani, M.

    2012-10-01

    The molecular complex of betaine with selenious acid namely, betaine dihydrogen selenite (C5H13NO5Se, BDHSe) was synthesised by the reaction of betaine and SeO2 in a 1:1:1 solution of isopropanol, methanol and water. Crystals were grown from this solution by cooling to 253 K for few days. The complex was formed without accompanying proton transfer from selenious acid molecule to betaine. The complete vibrational assignments and analysis of BDHSe have been performed by FTIR, FT-Raman and far-infrared spectral studies. More support on the experimental findings was added from the quantum chemical studies performed with DFT (B3LYP) method using 6-311++G∗∗, 6-31G∗∗, cc-pVDZ and 3-21G basis sets. The structural parameters, energies, thermodynamic parameters and the NBO charges of BDHSe were determined by the DFT method. The 1H and 13C isotropic chemical shifts (δ ppm) of BDHSe with respect to TMS were also calculated using the gauge independent atomic orbital (GIAO) method and compared with the experimental data. SHG experiment was carried out using Kurtz-Perry powder technique. The efficiency of second harmonic generation for BDHSe was estimated relatively to KDP: deff = 0.97 deff (KDP).

  2. Effect of hydrostatic pressure on the antiferroelectric phase transitions in ammonium dihydrogen arsenate NH4H2AsO4 and deuterated analogue

    International Nuclear Information System (INIS)

    Gesi, Kazuo; Ozawa, Kunio

    1984-01-01

    Effect of hydrostatic pressure on the antiferroelectric phase transitions in NH 4 H 2 AsO 4 and deuterated analogue (deuterium concentration --80%) was studied by dielectric constant measurements at high pressures up to about 0.8GPa. The transition temperature linearly decreases with increasing pressure with the ratios of -19.7K GPa -1 and -14.5K GPa -1 for NH 4 H 2 AsO 4 and the deuterated compound, respectively. The pressure effect is compared with previously reported results of other KH 2 PO 4 -type ferro- and antiferroelectric crystals. (author)

  3. Influence of ammonium nitrate on kinetics and mechanism of thermal decomposition of ammonium polyuranates

    International Nuclear Information System (INIS)

    Karelin, A.I.; Lobas, O.P.; Zhiganov, A.N.; Vasil'ev, K.F.; Zhiganova, A.A.

    1988-01-01

    The influence of ammonium nitrate on the mechanism and kinetics of dehydration and thermal decomposition of ammonium polyuranates was studied. An appreciable influence of the nitrate ion content in the samples of ammonium polyuranates on the development of thermal stability has been noted. The kinetic parameters of the thermal decomposition of ammonium polyuranates have been evaluated. A mechanism of the dehydration and thermal decomposition of ammonium polyuranates in the presence of ammonium nitrate has been proposed. It was shown that increase in the content of ammonium nitrate in the precipitate of ammonium polyuranates leads to a decrease in the specific surface of uranoso-uranic oxide

  4. Investigation of ammonium nitrate effect on kinetics and mechanism of thermal decomposition of ammonium polyuranates

    International Nuclear Information System (INIS)

    Karelin, A.I.; Lobas, O.P.; Zhiganov, A.N.; Vasil'ev, K.F.; Zhiganova, A.A.

    1987-01-01

    A study was made on ammonium nitrate effect on the mechanism and kinetics of dehydration and thermal decomposition of ammonium polyuranates. Sufficient effect of nitrate ion content in ammonium polyuranate samples on their thermal stability was noted. Kinetic parameters of thermal decomposition of ammonium polyuranates were evaluated. Mechanism of dehydration and thermal decomposition of ammonium polyuranates in the presence of ammonium nitrate was suggested. It was shown that increase of ammonium nitrate content in ammonium polyuranate precipitate resulted to reduction of the specific surface of prepared uranium mixed oxide

  5. Solidification of metallic aluminum on magnesium phosphate cements

    International Nuclear Information System (INIS)

    Lahalle, Hugo

    2016-01-01

    This work deals with the stabilization/solidification of radioactive waste using cement. More particularly, it aims at assessing the chemical compatibility between metallic aluminum and mortars based on magnesium phosphate cement. The physical and chemical processes leading to setting and hardening of the cement are first investigated. X-ray diffraction (XRD), thermogravimetry (TGA) and nuclear magnetic resonance spectroscopy ("3"1P and "1"1B MAS-NMR) are first used to characterize the solid phases formed during hydration, while inductively coupled plasma atomic emission spectroscopy analysis (ICP-AES), electrical conductometry and pH measurements provide information on the pore solution composition. Then, the corrosion of metallic aluminum in magnesium phosphate mortars is studied by monitoring the equilibrium potential and by electrochemical impedance spectroscopy (EIS). Magnesium phosphate cement is prepared from a mix of magnesium oxide (MgO) and potassium dihydrogen orthophosphate (KH_2PO_4). In the presence of water, hydration occurs according to a dissolution - precipitation process. The main hydrate is K-struvite (MgKPO_4.6H_2O). Its precipitation is preceded by that of two transient phases: phosphorrosslerite (MgHPO_4.7H_2O) and Mg_2KH(PO_4)_2.15H_2O. Boric acid retards cement hydration by delaying the formation of cement hydrates. Two processes may be involved in this retardation: the initial precipitation of amorphous or poorly crystallized minerals containing boron and phosphorus atoms, and/or the stabilization of cations (Mg"2"+, K"+) in solution. As compared with a Portland cement-based matrix, corrosion of aluminum is strongly limited in magnesium phosphate mortar. The pore solution pH is close to neutrality and falls within the passivation domain of aluminum. Corrosion depends on several parameters: it is promoted by a water-to-cement ratio (w/c) significantly higher than the chemical water demand of cement (w/c = 0.51), and by the addition of boric

  6. Solubility of ammonium metavanadate in ammonium carbonate and sodium bicarbonate solutions at 25 deg C

    International Nuclear Information System (INIS)

    Fedorov, P.I.; Andreev, V.K.; Slotvinskij-Sidak, N.P.

    1978-01-01

    Solubility at 25 deg C has been studied in the system ammonium metavanadate - sodium bicarbonate - water which is a stable section of the corresponding quaternary mutual system. In the eutonic point the content of ammonium metavanadate is 4.95% and of sodium bicarbonate 12.1%. The crystallization branch of ammonium metavanadate has been studied in the system ammonium metavanadate - ammonium carbonate - water at 25 deg C. Metavanadate solubility attains minimum (0.14%) at ammonium carbonate concentration 2.6%. Three sections have been studied of the quaternary system ammonium - metavanadate - ammonium carbonate - sodium bicarbonate-water at 25 deg C in the crystallization region of ammonium metavanadate at a ratio of sodium bicarbonate to ammonium carbonate 3:1, 1:1, and 1:3. A region of minimum solubility of ammonium metavanadate has been detected (0.1%)

  7. Optimization of nutritional requirements and ammonium feeding ...

    African Journals Online (AJOL)

    tounukarin

    2011-09-07

    Sep 7, 2011 ... Statistical experiment design and data analysis were used to ... Ammonium control strategies in fed-batch fermentation showed that when ammonium concentration ... environments, combined with the real-time process para-.

  8. High-resolution inelastic neutron scattering and neutron powder diffraction study of the adsorption of dihydrogen by the Cu(II) metal-organic framework material HKUST-1

    Science.gov (United States)

    Callear, Samantha K.; Ramirez-Cuesta, Anibal J.; David, William I. F.; Millange, Franck; Walton, Richard I.

    2013-12-01

    We present new high-resolution inelastic neutron scattering (INS) spectra (measured using the TOSCA and MARI instruments at ISIS) and powder neutron diffraction data (measured on the diffractometer WISH at ISIS) from the interaction of the prototypical metal-organic framework HKUST-1 with various dosages of dihydrogen gas. The INS spectra show direct evidence for the sequential occupation of various distinct sites for dihydrogen in the metal-organic framework, whose population is adjusted during increasing loading of the guest. The superior resolution of TOSCA reveals subtle features in the spectra, not previously reported, including evidence for split signals, while complementary spectra recorded on MARI present full information in energy and momentum transfer. The analysis of the powder neutron patterns using the Rietveld method shows a consistent picture, allowing the crystallographic indenisation of binding sites for dihydrogen, thus building a comprehensive picture of the interaction of the guest with the nanoporous host.

  9. Producing ammonium chloride from coal or shale

    Energy Technology Data Exchange (ETDEWEB)

    Christenson, O L

    1921-02-25

    Process of producing ammonium chloride consists of mixing the substance to be treated with a chloride of an alkali or alkaline earth metal, free silica, water and free hydrochloric acid, heating the mixture until ammonium chloride distills off and collecting the ammonium chloride.

  10. Development and manufacturing cycle for potassium nitrate and phosphate producing by conversion method

    Directory of Open Access Journals (Sweden)

    А. И. Алексеев

    2016-11-01

    Full Text Available Analysis of the Russian market of potash mineral fertilizers in 2014 and forecast for 2015-2019 show [http://businesstat.ru/images/demo/potash_fertilizers_russia.pdf] that today the most widespread potash fertilizer is  the potassium chloride. But chloride-free potassium-containing products are in the highest demand at the fertilizer market. One of possible solutions to this problem is recrystallization of the potassium chloride or potassium-containing mineral ores using nitrate-containing or phosphorus-containing salt products. The basis for justifying processing conditions for polymineral potassium-containing salt raw materials and salt mineral ores is the data on phase equilibria in multicomponent water-salt systems. Knowledge of the regularities of phase equilibria in multicomponent salt systems helps to develop optimal conditions for complex processing of polymineral natural and technical raw materials. Below it is present the results of technological calculations for processing potash mineral raw materials with account of the complex nature of its utilization. Based on the analysis of the solubility diagrams of mutual salt systems different cyclic processes for production of potassium dihydrogen phosphate and nitrate and sodium chloride from dihydrogen phosphate and sodium nitrate and potassium chloride by conversion method have been designed, and ways of these processes optimization have been proposed for reducing the cost of certain technical  operations.

  11. Sorption behavior of Zn(II) ions on synthetic apatitic calcium phosphates

    Science.gov (United States)

    Sebei, Haroun; Pham Minh, Doan; Nzihou, Ange; Sharrock, Patrick

    2015-12-01

    The synthesis, characterization and the reactivity of apatitic calcium phosphates (Ca-HA, chemical formula Ca10(PO4)6(OH)2) is reported. Calcium carbonate (CaCO3) and potassium dihydrogen orthophosphate (KH2PO4) were selected as economical starting materials for the synthesis of Ca-HA under atmospheric conditions. Monocalcium phosphate monohydrate (MCPM), dicalcium phosphate dihydrate (DCPD), and octacalcium phosphate pentahydrate (OCP) were identified as the main intermediates of the synthesis reaction. The product obtained after 48 h of reaction contains mainly low-crystalline Ca-HA and small amounts of other calcium phosphates such as octacalcium phosphate (OCP), B-type carbonate apatite (CAP), as well as unreacted calcium carbonate. This Ca-HA was found to be active for the removal of Zn2+ from an aqueous solution. Its sorption capacity reached up to 120 mg of Zn2+ per g of Ca-HA powder after 24 h of reaction. The monitoring of soluble Zn, Ca and P during the sorption experiment allowed characterizing the mechanism of Zn uptake. Dissolution-precipitation, ionic exchange and surface complexation are the three main mechanisms involved in the sorption processes. The contribution of these mechanisms is discussed in detail.

  12. Ammonium assmilation in spruce ectomycorrhizas

    International Nuclear Information System (INIS)

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

    1990-01-01

    Assimilation of labelled NH 4 + into amino acids has been followed in ectomycorrhizal roots of spruce. Over an 18 h period of NH 4 + 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 4 + 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 15 N enrichment in both amino and amido groups of glutamine. In contrast, the 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

  13. Bench-scale study of the effect of phosphate on an aerobic iron oxidation plant for mine water treatment.

    Science.gov (United States)

    Tischler, Judith S; Wiacek, Claudia; Janneck, Eberhard; Schlömann, Michael

    2014-01-01

    At the opencast pit Nochten acidic iron- and sulfate-rich mine waters are treated biotechnologically in a mine-water treatment plant by microbial iron oxidation. Due to the low phosphate concentration in such waters the treatment plant was simulated in bench-scale to investigate the influence of addition of potassium dihydrogen phosphate on chemical and biological parameters of the mine-water treatment. As a result of the phosphate addition the number of cells increased, which resulted in an increase of the iron oxidation rate in the reactor with phosphate addition by a factor of 1.7 compared to a reference approach without phosphate addition. Terminal restriction fragment length polymorphism (T-RFLP) analysis during the cultivation revealed a shift of the microbial community depending on the phosphate addition. While almost exclusively iron-oxidizing bacteria related to "Ferrovum" sp. were detected with phosphate addition, the microbial community was more diverse without phosphate addition. In the latter case, iron-oxidizing bacteria ("Ferrovum" sp., Acidithiobacillus spp.) as well as non-iron-oxidizing bacteria (Acidiphilium sp.) were identified. Copyright © 2013 Elsevier Ltd. All rights reserved.

  14. Headspace Analysis of Ammonium Nitrate

    Science.gov (United States)

    2017-01-25

    explosive ammonium nitrate produces ammonia and nitric acid in the gaseous headspace above bulk solids, but the concentrations of the products have been...and NO2-, a product of nitrate fragmentation (Figure 7). Brief spikes in the background and dips in oxalic acid signal were observed at the time of...either filtered air or experimental nitric acid vapor sources so that analyte signal could be measured directly opposite background. With oxalic

  15. Damage and other changes that occur in some inorganic materials subjected to synchrotron radiation

    International Nuclear Information System (INIS)

    Bhat, H.L.; Sheen, D.B.; Sherwood, J.N.

    1983-01-01

    The subject is discussed under the headings: introduction (general description of white radiation topography experiments with the Daresbury SRS); experimental; results and discussion (ammonium perchlorate - orthorhombic lattice; sodium nitrate -rhombohedral lattice; sodium chlorate - modified cubic lattice; ammonium dihydrogen phosphate - tetragonal lattice; calcium carbonate - trigonal lattice). Mechanisms for the radiation effects observed are proposed. (U.K.)

  16. Leaching of Cu, Cd, Pb, and phosphorus and their availability in the phosphate-amended contaminated soils under simulated acid rain.

    Science.gov (United States)

    Cui, Hongbiao; Zhang, Shiwen; Li, Ruyan; Yi, Qitao; Zheng, Xuebo; Hu, Youbiao; Zhou, Jing

    2017-09-01

    Phosphate amendments have been used to immobilize heavy metal-contaminated soils. However, phosphate amendments contain large amounts of phosphorus, which could leach out to potentially contaminate groundwater and surface water. A laboratory column leaching experiment was designed to study the effects of simulated acid rain (SAR) on the potential release of copper (Cu), lead (Pb), cadmium (Cd), and phosphorus (P), and their availability after immobilizing with hydroxyapatite (HAP) and potassium dihydrogen phosphate (PDP). The application of HAP and PDP enhanced the leachate electrical conductivity, total organic carbon, and pH. Higher P was found in the PDP- (>4.29 mg L -1 ) and HAP-treated (>1.69 mg L -1 ) columns than that in untreated (phosphate amendments might promote the leaching of some metals while immobilizing others.

  17. Treating ammonium-rich wastewater with sludge from water treatment plant to produce ammonium alum

    Directory of Open Access Journals (Sweden)

    Wen-Po Cheng

    2016-03-01

    Full Text Available This study applies a process to treat ammonium-rich wastewater using alum-generated sludge form water purification plant, and gain economic benefit by producing ammonium alum (Al(NH4(SO42·12H2O. The factors affecting production of ammonium alum include molar ratio of ammonium to aluminum concentration, sulfuric acid concentration, mixing speed, mixing time, standing time, and temperature. According to the equation for the ammonium removal reaction, the theoretical quantity of ammonium alum was calculated based on initial and final concentrations of ammonium. Then, the weight of ammonium alum crystal was divided by the theoretical weight to derive the recovery ratio. The optimum sludge and sulfuric acid dosage to treat about 17 g L−1 ammonium wastewater are 300 g L−1 and 100 mL L−1, respectively. The optimal dosage for wastewater is molar ratio of ammonium to aluminum of about 1 due to the aluminum dissolving in acidified wastewater. The ammonium removal efficiency is roughly 70% and the maximum recovery ratio for ammonium alum is 93% when the wastewater is mixed for 10 min at the mixing velocity gradient of 100 s−1. Ammonium alum production or ammonium removal can be enhanced by controlling the reaction at low temperatures.

  18. High-resolution inelastic neutron scattering and neutron powder diffraction study of the adsorption of dihydrogen by the Cu(II) metal–organic framework material HKUST-1

    Energy Technology Data Exchange (ETDEWEB)

    Callear, Samantha K.; Ramirez-Cuesta, Anibal J.; David, William I.F. [ISIS Facility, Rutherford Appleton Laboratory, Harwell Science and Innovation Campus, Didcot, OX11 0QX (United Kingdom); Millange, Franck [Institut Lavoisier Versailles (CNRS UMR 8180), Université de Versailles, 78035 Versailles (France); Walton, Richard I., E-mail: r.i.walton@warwick.ac.uk [Department of Chemistry, University of Warwick, CV4 7AL, Coventry (United Kingdom)

    2013-12-12

    Highlights: • Binding sites for dihydrogen in a metal–organic framework have been identified. • The combination of diffraction and spectroscopy shows competitive filling of various adsorption sites. • Inelastic neutron scattering over wide-momentum transfer reveals new models for hydrogen-framework interactions. - Abstract: We present new high-resolution inelastic neutron scattering (INS) spectra (measured using the TOSCA and MARI instruments at ISIS) and powder neutron diffraction data (measured on the diffractometer WISH at ISIS) from the interaction of the prototypical metal–organic framework HKUST-1 with various dosages of dihydrogen gas. The INS spectra show direct evidence for the sequential occupation of various distinct sites for dihydrogen in the metal–organic framework, whose population is adjusted during increasing loading of the guest. The superior resolution of TOSCA reveals subtle features in the spectra, not previously reported, including evidence for split signals, while complementary spectra recorded on MARI present full information in energy and momentum transfer. The analysis of the powder neutron patterns using the Rietveld method shows a consistent picture, allowing the crystallographic indenisation of binding sites for dihydrogen, thus building a comprehensive picture of the interaction of the guest with the nanoporous host.

  19. High-resolution inelastic neutron scattering and neutron powder diffraction study of the adsorption of dihydrogen by the Cu(II) metal–organic framework material HKUST-1

    International Nuclear Information System (INIS)

    Callear, Samantha K.; Ramirez-Cuesta, Anibal J.; David, William I.F.; Millange, Franck; Walton, Richard I.

    2013-01-01

    Highlights: • Binding sites for dihydrogen in a metal–organic framework have been identified. • The combination of diffraction and spectroscopy shows competitive filling of various adsorption sites. • Inelastic neutron scattering over wide-momentum transfer reveals new models for hydrogen-framework interactions. - Abstract: We present new high-resolution inelastic neutron scattering (INS) spectra (measured using the TOSCA and MARI instruments at ISIS) and powder neutron diffraction data (measured on the diffractometer WISH at ISIS) from the interaction of the prototypical metal–organic framework HKUST-1 with various dosages of dihydrogen gas. The INS spectra show direct evidence for the sequential occupation of various distinct sites for dihydrogen in the metal–organic framework, whose population is adjusted during increasing loading of the guest. The superior resolution of TOSCA reveals subtle features in the spectra, not previously reported, including evidence for split signals, while complementary spectra recorded on MARI present full information in energy and momentum transfer. The analysis of the powder neutron patterns using the Rietveld method shows a consistent picture, allowing the crystallographic indenisation of binding sites for dihydrogen, thus building a comprehensive picture of the interaction of the guest with the nanoporous host

  20. Prevention of radioactive contamination in the manufacture of phosphate fertilizers; Prevencion de contaminacion radiactiva en la fabricacion de fertilizantes fosfatados

    Energy Technology Data Exchange (ETDEWEB)

    Romero G, E T

    1996-12-31

    In this work was studied the separation of uranium from the phosphate rock to decrease the level of radioactivity in the phosphate fertilizers, this prevents the redistribution of uranium in the environment. The uranium leaching conditions from phosphate rock were estimated using alkaline solutions. The changes in the natural phosphate rock after leaching were studied. The amenability to separate the uranium from phosphate rock with ammonium carbonate / bicarbonate solution was determined. The uranium extraction was approximately 40%. The leaching conditions showed high selectivity for uranium without changes in the ore structure. The bulk ore was not dissolved. (Author).

  1. Glufosinate ammonium selection of transformed Arabidopsis.

    Science.gov (United States)

    Weigel, Detlef; Glazebrook, Jane

    2006-12-01

    INTRODUCTIONOne of the most commonly used markers for the selection of transgenic Arabidopsis is resistance to glufosinate ammonium, an herbicide that is sold under a variety of trade names including Basta and Finale. Resistance to glufosinate ammonium is conferred by the bacterial bialophos resistance gene (BAR) encoding the enzyme phosphinotricin acetyl transferase (PAT). This protocol describes the use of glufosinate ammonium to select transformed Arabidopsis plants. The major advantage of glufosinate ammonium selection is that it can be performed on plants growing in soil and does not require the use of sterile techniques.

  2. 76 FR 46907 - Ammonium Nitrate Security Program

    Science.gov (United States)

    2011-08-03

    ... Maritime Transportation Security Act NAICS North American Industrial Classification System NPRM Notice of.... Commenters noted, for example, that equipment used for transporting bulk ammonium nitrate, such as hoppers...

  3. Uranium from phosphate ores

    International Nuclear Information System (INIS)

    Hurst, F.J.

    1983-01-01

    The following topics are described briefly: the way phosphate fertilizers are made; how uranium is recovered in the phosphate industry; and how to detect covert uranium recovery operations in a phsophate plant

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

    Science.gov (United States)

    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 with...

  5. Ammonium-induced inhibition of ammonium-starved Nitrosomonas europaea cells in soil and sand slurries

    NARCIS (Netherlands)

    Gerards, S.; Duyts, H.; Laanbroek, H.J.

    1998-01-01

    Ammonia-oxidising bacteria are poor competitors for limiting amounts of ammonium. Hence, starvation for ammonium seems to be the regular condition for these bacteria in natural environments. Long-term survival in the absence of ammonium will be dependent on the ability to maintain large population

  6. Precipitation of ammonium from concentrated industrial wastes as struvite: a search for the optimal reagents.

    Science.gov (United States)

    Borojovich, Eitan J C; Münster, Meshulam; Rafailov, Gennady; Porat, Ze'ev

    2010-07-01

    Precipitation of struvite (MgNH4PO4) is a known process for purification of wastewater from high concentrations of ammonium. The optimal conditions for precipitation are basic pH (around 9) and sufficient concentrations of magnesium and phosphate ions. In this work, we accomplished efficient precipitation of ammonium from concentrated industrial waste stream by using magnesium oxide (MgO) both as a source of magnesium ions and as a base. Best results were obtained with technical-grade MgO, which provided 99% removal of ammonium. Moreover, ammonium removal occurred already at pH 7, and the residual ammonium concentration (50 mg/L) remained constant upon addition of more MgO without rising again, as occurs with sodium hydroxide (NaOH). This process may have two other advantages; it also can be relevant for the problem of uncontrolled precipitation of struvite in the supernatant of anaerobic sludge treatment plants, and the precipitate can be used as a fertilizer.

  7. Determination of ammonium on an integrated microchip with LED-induced fluorescence detection.

    Science.gov (United States)

    Xue, Shuhua; Uchiyama, Katsumi; Li, Hai-Fang

    2012-01-01

    A simply fabricated microfluidic device integrated with a fluorescence detection system has been developed for on-line determination of ammonium in aqueous samples. A 365-nm light-emitting diode (LED) as an excitation source and a minor band pass filter were mounted into a polydimethylsiloxane (PDMS)-based microchip for the purpose of miniaturization of the entire analytical system. The ammonium sample reacted with o-phthaldialdehyde (OPA) on-chip with sodium sulfite as reducing reagent to produce a fluorescent isoindole derivative, which can emit fluorescence signal at about 425 nm when excited at 365 nm. Effects of pH, flow rate of solutions, concentrations of OPA-reagent, phosphate and sulfite salt were investigated. The calibration curve of ammonium in the range of 0.018-1.8 microg/mL showed a good linear relationship with R2 = 0.9985, and the detection limit was (S/N = 3) 3.6 x 10(-4) microg/mL. The relative standard deviation was 2.8% (n = 11) by calculating at 0.18 microg/mL ammonium for repeated detection. The system was applied to determine the ammonium concentration in rain and river waters, even extent to other analytes fluorescence detection by the presented device.

  8. Phase diagram of ammonium nitrate

    International Nuclear Information System (INIS)

    Dunuwille, Mihindra; Yoo, Choong-Shik

    2013-01-01

    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 2 , N 2 O, and H 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 ′ transition above 17 GPa and provide new constraints for the melting and phase diagram of AN to 40 GPa and 400°C

  9. Photosynthesis of ammonium uranous fluoride

    International Nuclear Information System (INIS)

    El-Fekey, S.A.; Zaki, M.R.; Farah, M.Y.

    1975-01-01

    This study pertains to utilisation of solar energy for ethanol photosynthesis of ammonium uranous fluoride, that satisfies nuclear specifications needed for calcio- or magnesiothermy. Insolation in autumn using 4-10% ethanol in 5-20 g uranium/litre at initial pH 3.25 gave practically 99.8% yield in two hours, independant of 1.0 to 2.0 stoichiometric NH 4 F. With ultraviolet light, the yield varied between 30 and 60%, even after four hours irradiation. Stirring and heating to 60 0 C raised the tap density of the dried double fluorides from 1.48 at 30 0 C, to 1.85 g/cm 3 at 60 0 C. The texture increased also in fineness to 100% 50μ aggregates. The powders satisfy nuclear purity specifications. Thermograms indicated preferential decomposition of double fluoride at 375 0 C in controlled atmosphere to obtain nuclear pure anhydrous uranium tetrafluoride

  10. Atmospheric behaviour of ammonia and ammonium

    NARCIS (Netherlands)

    Asman, W.A.H.

    1987-01-01

    1.4.1 Scope of this thesis

    A few models for ammonia and ammonium exist. Russell et al. (1983) made a multi-layer Lagrangian transport model describing the transport and formation of ammonium nitrate aerosol for California. They did not take reactions of ammonia and sulphuric acid

  11. 21 CFR 582.1135 - Ammonium bicarbonate.

    Science.gov (United States)

    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 Food Additives § 582.1135 Ammonium bicarbonate. (a)...

  12. Thermal analysis studies of ammonium uranyl carbonate

    International Nuclear Information System (INIS)

    Cao Xinsheng; Ma Xuezhong; Wang Fapin; Liu Naixin; Ji Changhong

    1988-01-01

    The simultaneous thermogravimetry and differential thermal analysis of the ammonium uranyl carbonate powder were performed with heat balance in the following atmosphers: Air, Ar and Ar-8%H 2 . The thermogravimetry and differential thermal analysis curves of the ammonium uranyl carbonate powder obtained from different source were reported and discussed

  13. Ammonium nitrate-potassium nitrate system

    Energy Technology Data Exchange (ETDEWEB)

    Cady, H.H.

    1981-01-01

    A portion of the binary phase diagram for the system ammonium nitrate-potassium nitrate has been determined from -55/sup 0/C to 185/sup 0/C. Results are presented for the ammonium-nitrate-rich end of the system up to 30 wt% potassium nitrate.

  14. Combination of struvite pyrolysate recycling with mixed-base technology for removing ammonium from fertilizer wastewater.

    Science.gov (United States)

    Yu, Rongtai; Geng, Jinju; Ren, Hongqiang; Wang, Yanru; Xu, Ke

    2012-11-01

    Removal of ammonium from wastewater via struvite (MAP) pyrolysate recycling combined with a mixed-base NaOH/Mg(OH)(2) technology was investigated, and the phosphate and magnesium concentration in the supernatant were measured. The optimal parameters for acidolysis were a pH of 1; temperature of 120°C and time of 2h. The presence of derivatives of amorphous magnesium hydrogen phosphate (MgHPO(4)), namely magnesium phosphate (Mg(3)(PO(4))(2)) and magnesium pyrophosphate (Mg(2)P(2)O(7)) were verified by experiment. The ammonium removal ratio in this combined mixed-base technology was 96.8% in the first cycle, 80.6% in the second, and 81.0% after acidolysis. The phosphate and magnesium ions concentration in the supernatant were about 1mg/L and 40 mg/L, respectively. The grain size of MAP was 1.52 nm without seeding and 1.79 nm with seeding, and the growth rate of MAP was 17.6%. Copyright © 2012 Elsevier Ltd. All rights reserved.

  15. 49 CFR 176.415 - Permit requirements for Division 1.5, ammonium nitrates, and certain ammonium nitrate fertilizers.

    Science.gov (United States)

    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 than...

  16. Phosphate acquisition efficiency and phosphate starvation tolerance ...

    Indian Academy of Sciences (India)

    3Department of Genetics and Plant Breeding, College of Agriculture, Lembucherra, Tripura 799 ... vated in soil like red and lateritic or acid, with low soluble phosphate content. ..... activation of genes involved in the adaptation of Arabidopsis to.

  17. Gibbs free energy of transfer of a methylene group on {UCON + (sodium or potassium) phosphate salts} aqueous two-phase systems: Hydrophobicity effects

    International Nuclear Information System (INIS)

    Silverio, Sara C.; Rodriguez, Oscar; Teixeira, Jose A.; Macedo, Eugenia A.

    2010-01-01

    The Gibbs free energy of transfer of a suitable hydrophobic probe can be regarded as a measure of the relative hydrophobicity of the different phases. The methylene group (CH 2 ) can be considered hydrophobic, and thus be a suitable probe for hydrophobicity. In this work, the partition coefficients of a series of five dinitrophenylated-amino acids were experimentally determined, at 23 o C, in three different tie-lines of the biphasic systems: (UCON + K 2 HPO 4 ), (UCON + potassium phosphate buffer, pH 7), (UCON + KH 2 PO 4 ), (UCON + Na 2 HPO 4 ), (UCON + sodium phosphate buffer, pH 7), and (UCON + NaH 2 PO 4 ). The Gibbs free energy of transfer of CH 2 units were calculated from the partition coefficients and used to compare the relative hydrophobicity of the equilibrium phases. The largest relative hydrophobicity was found for the ATPS formed by dihydrogen phosphate salts.

  18. Availability of native and added phosphates for the soil

    International Nuclear Information System (INIS)

    Scivittaro, W.B.; Boaretto, A.E.; Muraoka, T.

    1995-01-01

    In superficial composite samples of two Red-Yellow Latosols with different physical and chemical properties, analyses were carried out on inorganic form of phosphorus as well as the availability of native and added phosphates. The method applied was soil phosphorus fractionation associated with isotopic dilution technique ( 32 P). The samples were taken from pots containing soils incubated for a month with fluid phosphatic fertilizers (phosphoric acid and 10-30-00 suspension) and solid phosphatic fertilizers (mono ammonium phosphate and triple superphosphate), at the rate of 210 mg P 2 O 5 /kg of soil. A control treatment was included. In both soils the availability of inorganic phosphorus fractions decreased at the following order: H 2 O-P > Al-P > Fe-P > CA-P > occluded-P. The water soluble and aluminium phosphates represented the main source of available P for the newly fertilizer, the iron phosphates were also an important source of available phosphorus. The soil phosphorus fixing capacity influenced the availability of native and added phosphates. (author). 17 refs, 3 tabs

  19. Electro-activity of cobalt and nickel complexes for the reduction of protons into di-hydrogen. Application to PEM water electrolysis

    International Nuclear Information System (INIS)

    Pantani, O.; Anxolabehere, E.; Aukauloo, A.; Millet, P.

    2006-01-01

    Proton exchange membrane (PEM) water electrolysis is a safe and efficient way to perform water splitting into di-hydrogen and di-oxygen. In a PEM water electrolyser, platinum is commonly used as electro-catalyst on the cathodic side of the cells, mostly because of its efficiency for hydrogen evolution. But for cost considerations, there is a need to find alternative low-cost electrocatalysts. Molecular chemistry offers the possibility of synthesizing new compounds for this purpose, such as transition metal complexes. Results obtained with nickel- and cobalt-oximes compounds are presented in this paper. They have been chemically (1H NMR, EPR) and electrochemically (voltametry, spectro-electrochemistry) characterized. Their ability to electrochemically reduce protons into di-hydrogen when they are either dissolved in solution or immobilized at the surface of a solid electrode is discussed. (authors)

  20. Capacity and mechanisms of ammonium and cadmium sorption on different wetland-plant derived biochars

    International Nuclear Information System (INIS)

    Cui, Xiaoqiang; Hao, Hulin; Zhang, Changkuan; He, Zhenli; Yang, Xiaoe

    2016-01-01

    The objective of this study was to investigate the relationship between Cd 2+ /NH 4 + sorption and physicochemical properties of biochars produced from different wetland plants. Biochars from six species of wetland plants (i.e., Canna indica, Pennisetum purpureum Schum, Thalia dealbata, Zizania caduciflora, Phragmites australis and Vetiveria zizanioides) were obtained at 500 °C and characterized, and their sorption for ammonium and cadmium was determined. There were significant differences in elemental composition, functional groups and specific surface area among the biochars derived from different wetland plant species. Sorption of ammonium and cadmium on the biochars could be described by a pseudo second order kinetic model, and the simple Langmuir model fits the isotherm data better than the Freundlich or Temkin model. The C. indica derived biochar had the largest sorption capacity for NH 4 + and Cd 2+ , with a maximum sorption of 13.35 and 125.8 mg g −1 , respectively. P. purpureum Schum derived biochar had a similar maximum sorption (119.3 mg g −1 ) for Cd 2+ . Ammonium sorption was mainly controlled by cation exchange, surface complexation with oxygen-containing functional groups and the formation of magnesium ammonium phosphate compounds, whereas for Cd 2+ sorption, the formation of cadmium phosphate precipitates, cation exchange and binding to oxygen-containing groups were the major possible mechanisms. In addition, the sorption of ammonium and cadmium was not affected by surface area and microporosity of the biochars. - Highlights: • Biochars varied in physicochemical properties and adsorption capacity. • Canna indica derived biochar has a high sorption capacity for Cd 2+ . • NH 4 + and Cd 2+ sorption on biochars fits a pseudo second order and Langmuir model. • Sorption mechanism is related to complexation, cation exchange and precipitation.

  1. Capacity and mechanisms of ammonium and cadmium sorption on different wetland-plant derived biochars

    Energy Technology Data Exchange (ETDEWEB)

    Cui, Xiaoqiang [Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058 (China); Hao, Hulin [Ningbo Raw Water Resource Research Academy, Ningbo (China); Zhang, Changkuan [Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058 (China); He, Zhenli [Indian River Research and Education Center, Institute of Food and Agricultural Sciences, University of Florida, Fort Pierce, FL 34945 (United States); Yang, Xiaoe, E-mail: xyang571@yahoo.com [Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058 (China)

    2016-01-01

    The objective of this study was to investigate the relationship between Cd{sup 2+}/NH{sub 4}{sup +} sorption and physicochemical properties of biochars produced from different wetland plants. Biochars from six species of wetland plants (i.e., Canna indica, Pennisetum purpureum Schum, Thalia dealbata, Zizania caduciflora, Phragmites australis and Vetiveria zizanioides) were obtained at 500 °C and characterized, and their sorption for ammonium and cadmium was determined. There were significant differences in elemental composition, functional groups and specific surface area among the biochars derived from different wetland plant species. Sorption of ammonium and cadmium on the biochars could be described by a pseudo second order kinetic model, and the simple Langmuir model fits the isotherm data better than the Freundlich or Temkin model. The C. indica derived biochar had the largest sorption capacity for NH{sub 4}{sup +} and Cd{sup 2+}, with a maximum sorption of 13.35 and 125.8 mg g{sup −1}, respectively. P. purpureum Schum derived biochar had a similar maximum sorption (119.3 mg g{sup −1}) for Cd{sup 2+}. Ammonium sorption was mainly controlled by cation exchange, surface complexation with oxygen-containing functional groups and the formation of magnesium ammonium phosphate compounds, whereas for Cd{sup 2+} sorption, the formation of cadmium phosphate precipitates, cation exchange and binding to oxygen-containing groups were the major possible mechanisms. In addition, the sorption of ammonium and cadmium was not affected by surface area and microporosity of the biochars. - Highlights: • Biochars varied in physicochemical properties and adsorption capacity. • Canna indica derived biochar has a high sorption capacity for Cd{sup 2+}. • NH{sub 4}{sup +} and Cd{sup 2+} sorption on biochars fits a pseudo second order and Langmuir model. • Sorption mechanism is related to complexation, cation exchange and precipitation.

  2. Degradation processes of reinforced concretes by combined sulfate–phosphate attack

    International Nuclear Information System (INIS)

    Secco, Michele; Lampronti, Giulio Isacco; Schlegel, Moritz-Caspar; Maritan, Lara; Zorzi, Federico

    2015-01-01

    A novel form of alteration due to the interaction between hydrated cement phases and sulfate and phosphate-based pollutants is described, through the characterization of concrete samples from an industrial reinforced concrete building. Decalcification of the cement matrices was observed, with secondary sulfate and phosphate-based mineral formation, according to a marked mineralogical and textural zoning. Five alteration layers may be detected: the two outermost layers are characterized by the presence of gypsum–brushite solid solution phases associated with anhydrous calcium sulfates and phosphates, respectively, while a progressive increase in apatite and ammonium magnesium phosphates is observable in the three innermost layers, associated with specific apatite precursors (brushite, octacalcium phosphate and amorphous calcium phosphate, respectively). The heterogeneous microstructural development of secondary phases is related to the chemical, pH and thermal gradients in the attacked cementitious systems, caused by different sources of pollutants and the exposure to the sun's radiation

  3. Degradation processes of reinforced concretes by combined sulfate–phosphate attack

    Energy Technology Data Exchange (ETDEWEB)

    Secco, Michele, E-mail: michele.secco@unipd.it [Inter-Departmental Research Center for the Study of Cement Materials and Hydraulic Binders (CIRCe), University of Padova, Via Gradenigo 6, 35131 Padova (Italy); Department of Civil, Environmental and Architectural Engineering (ICEA), University of Padova, Via Marzolo 9, 35131 Padova (Italy); Lampronti, Giulio Isacco, E-mail: gil21@cam.ac.uk [Department of Earth Sciences, University of Cambridge, Downing Street, CB2 3EQ Cambridge (United Kingdom); Schlegel, Moritz-Caspar, E-mail: moritz-caspar.schlegel@helmholtz-berlin.de [BAM Federal Institute for Materials Research and Testing, Unter den Eichen 87, 12205 Berlin (Germany); Helmholtz-Zentrum Berlin fürMaterialien und Energie GmbH, Hahn-Meitner-Platz 1, 14109 Berlin (Germany); Maritan, Lara, E-mail: lara.maritan@unipd.it [Department of Geosciences, University of Padova, Via Gradenigo 6, 35131 Padova (Italy); Zorzi, Federico, E-mail: federico.zorzi@unipd.it [Department of Geosciences, University of Padova, Via Gradenigo 6, 35131 Padova (Italy)

    2015-02-15

    A novel form of alteration due to the interaction between hydrated cement phases and sulfate and phosphate-based pollutants is described, through the characterization of concrete samples from an industrial reinforced concrete building. Decalcification of the cement matrices was observed, with secondary sulfate and phosphate-based mineral formation, according to a marked mineralogical and textural zoning. Five alteration layers may be detected: the two outermost layers are characterized by the presence of gypsum–brushite solid solution phases associated with anhydrous calcium sulfates and phosphates, respectively, while a progressive increase in apatite and ammonium magnesium phosphates is observable in the three innermost layers, associated with specific apatite precursors (brushite, octacalcium phosphate and amorphous calcium phosphate, respectively). The heterogeneous microstructural development of secondary phases is related to the chemical, pH and thermal gradients in the attacked cementitious systems, caused by different sources of pollutants and the exposure to the sun's radiation.

  4. Specific electrical conductivity in molten potassium dihydrogen phosphate KH2PO4 - An electrolyte for water electrolysis at ∼300°C

    DEFF Research Database (Denmark)

    Nikiforov, Aleksey Valerievich; Berg, Rolf W.; Petrushina, Irina

    2016-01-01

    The conductivity of pure molten KH2PO4 salt and four mixtures with more or less water (KH2PO4-H2O and KH2PO4-KPO3 systems, respectively) were measured at temperatures of 240-320°C and under their own water vapor pressures. Molten KH2PO4 has been proven to be a promising electrolyte for an elevated...... temperature pressurized water electrolyzer demonstrating high conductivity of ∼0.30Scm-1 at 300°C. The conductivity data are given as polynomial functions of temperature and composition. The melting point of the pure salt under its own water vapor pressure was determined to be ∼272°C....

  5. Specific electrical conductivity in molten potassium dihydrogen phosphate KH2PO4 - An electrolyte for water electrolysis at ∼300°C

    DEFF Research Database (Denmark)

    Nikiforov, Aleksey Valerievich; Berg, Rolf W.; Petrushina, Irina

    2016-01-01

    The conductivity of pure molten KH2PO4 salt and four mixtures with more or less water (KH2PO4-H2O and KH2PO4-KPO3 systems, respectively) were measured at temperatures of 240-320°C and under their own water vapor pressures. Molten KH2PO4 has been proven to be a promising electrolyte for an elevated...

  6. Gas phase 1H NMR studies and kinetic modeling of dihydrogen isotope equilibration catalyzed by Ru-nanoparticles under normal conditions: dissociative vs. associative exchange.

    Science.gov (United States)

    Limbach, Hans-Heinrich; Pery, Tal; Rothermel, Niels; Chaudret, Bruno; Gutmann, Torsten; Buntkowsky, Gerd

    2018-04-25

    The equilibration of H2, HD and D2 between the gas phase and surface hydrides of solid organic-ligand-stabilized Ru metal nanoparticles has been studied by gas phase 1H NMR spectroscopy using closed NMR tubes as batch reactors at room temperature and 800 mbar. When two different nanoparticle systems, Ru/PVP (PVP ≡ polyvinylpyrrolidone) and Ru/HDA (HDA ≡ hexadecylamine) were exposed to D2 gas, only the release of HD from the hydride containing surface could be detected in the initial stages of the reaction, but no H2. In the case of Ru/HDA also the reverse experiment was performed where surface deuterated nanoparticles were exposed to H2. In that case, the conversion of H2 into gaseous HD was detected. In order to analyze the experimental kinetic and spectroscopic data, we explored two different mechanisms taking into account potential kinetic and equilibrium H/D isotope effects. Firstly, we explored the dissociative exchange mechanism consisting of dissociative adsorption of dihydrogen, fast hydride surface diffusion and associative desorption of dihydrogen. It is shown that if D2 is the reaction partner, only H2 will be released in the beginning of the reaction, and HD only in later reaction stages. The second mechanism, dubbed here associative exchange consists of the binding of dihydrogen to Ru surface atoms, followed by a H-transfer to or by H-exchange with an adjacent hydride site, and finally of the associative desorption of dihydrogen. In that case, in the exchange with D2, only HD will be released in the beginning of the reaction. Our experimental results are not compatible with the dissociative exchange but can be explained in terms of the associative exchange. Whereas the former will dominate at low temperatures and pressures, the latter will prevail around room temperature and normal pressures where transition metal nanoparticles are generally used as reaction catalysts.

  7. A quantum dynamical study of the rotation of the dihydrogen ligand in the Fe(H)2(H2)(PEtPh2)3 coordination complex

    Science.gov (United States)

    Gonzalez, Megan E.; Eckert, Juergen; Aquino, Adelia J. A.; Poirier, Bill

    2018-04-01

    Progress in the hydrogen fuel field requires a clear understanding and characterization of how materials of interest interact with hydrogen. Due to the inherently quantum mechanical nature of hydrogen nuclei, any theoretical studies of these systems must be treated quantum dynamically. One class of material that has been examined in this context are dihydrogen complexes. Since their discovery by Kubas in 1984, many such complexes have been studied both experimentally and theoretically. This particular study examines the rotational dynamics of the dihydrogen ligand in the Fe(H)2(H2)(PEtPh2)3 complex, allowing for full motion in both the rotational degrees of freedom and treating the quantum dynamics (QD) explicitly. A "gas-phase" global potential energy surface is first constructed using density functional theory with the Becke, 3-parameter, Lee-Yang-Parr functional; this is followed by an exact QD calculation of the corresponding rotation/libration states. The results provide insight into the dynamical correlation of the two rotation angles as well as a comprehensive analysis of both ground- and excited-state librational tunneling splittings. The latter was computed to be 6.914 cm-1—in excellent agreement with the experimental value of 6.4 cm-1. This work represents the first full-dimensional ab initio exact QD calculation ever performed for dihydrogen ligand rotation in a coordination complex.

  8. Phase diagram of ammonium nitrate

    Energy Technology Data Exchange (ETDEWEB)

    Dunuwille, Mihindra; Yoo, Choong-Shik, E-mail: csyoo@wsu.edu [Department of Chemistry and Institute for Shock Physics, Washington State University, Pullman, Washington 99164 (United States)

    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.

  9. Zinc phosphate conversion coatings

    Science.gov (United States)

    Sugama, Toshifumi

    1997-01-01

    Zinc phosphate conversion coatings for producing metals which exhibit enhanced corrosion prevention characteristics are prepared by the addition of a transition-metal-compound promoter comprising a manganese, iron, cobalt, nickel, or copper compound and an electrolyte such as polyacrylic acid, polymethacrylic acid, polyitaconic acid and poly-L-glutamic acid to a phosphating solution. These coatings are further improved by the incorporation of Fe ions. Thermal treatment of zinc phosphate coatings to generate .alpha.-phase anhydrous zinc phosphate improves the corrosion prevention qualities of the resulting coated metal.

  10. Struvite pyrolysate recycling combined with dry pyrolysis for ammonium removal from wastewater.

    Science.gov (United States)

    Yu, Rongtai; Geng, Jinju; Ren, Hongqiang; Wang, Yanru; Xu, Ke

    2013-03-01

    The dry pyrolysis of magnesium ammonium phosphate (MAP) with NaOH powder for ammonium release was investigated, as well as the utility of MAP pyrolysate recycling. The identities of the MAP pyrolysate and its derivatives were experimentally validated. The results showed that the pyrolysate was amorphous magnesium hydrogen phosphate (MgHPO4) and magnesium pyrophosphate (Mg2P2O7). The best molar ratio of sodium hydroxide (NaOH) powder to ammonium was 1:1, at 110°C for 3h. The optimum pH for pyrolysate recycling was 9.5. The ammonia removal ratio could be maintained above 80% with MAP pyrolysate recycling. Seed crystal inoculation increased the rate of MAP crystallization by 20.86%, as well as the MAP grain size (2.08nm with seeding versus 1.72nm without). MAP particle size with NaOH treatment decreased: d(0.5)=19.34μm versus d(0.5)=30.35μm for direct pyrolysis. The results demonstrated that crystal growth was controlled by adding NaOH during MAP pyrolysis. Copyright © 2013 Elsevier Ltd. All rights reserved.

  11. Ab Initio Electronic Structure Calculation of [4Fe-3S] Cluster of Hydrogenase as Dihydrogen Dissociation/Production Catalyst

    Science.gov (United States)

    Kim, Jaehyun; Kang, Jiyoung; Nishigami, Hiroshi; Kino, Hiori; Tateno, Masaru

    2018-03-01

    Hydrogenases catalyze both the dissociation and production of dihydrogen (H2). Most hydrogenases are inactivated rapidly and reactivated slowly (in vitro), in the presence of dioxygen (O2) and H2, respectively. However, membrane-bound [NiFe] hydrogenases (MBHs) sustain their activity even together with O2, which is termed "O2 tolerance". In previous experimental analyses, an MBH was shown to include a hydroxyl ion (OH-) bound to an Fe of the super-oxidized [4Fe-3S]5+ cluster in the proximity of the [NiFe] catalytic cluster. In this study, the functional role of the OH- in the O2 tolerance was investigated by ab initio electronic structure calculation of the [4Fe-3S] proximal cluster. The analysis revealed that the OH- significantly altered the electronic structure, thereby inducing the delocalization of the lowest unoccupied molecular orbital (LUMO) toward the [NiFe] catalytic cluster, which may intermediate the electron transfer between the catalytic and proximal clusters. This can promote the O2-tolerant catalytic cycle in the hydrogenase reaction.

  12. Dual gas-diffusion membrane- and mediatorless dihydrogen/air-breathing biofuel cell operating at room temperature

    Science.gov (United States)

    Xia, Hong-qi; So, Keisei; Kitazumi, Yuki; Shirai, Osamu; Nishikawa, Koji; Higuchi, Yoshiki; Kano, Kenji

    2016-12-01

    A membraneless direct electron transfer (DET)-type dihydrogen (H2)/air-breathing biofuel cell without any mediator was constructed wherein bilirubin oxidase from Myrothecium verrucaria (BOD) and membrane-bound [NiFe] hydrogenase from Desulfovibrio vulgaris Miyazaki F (MBH) were used as biocatalysts for the cathode and the anode, respectively, and Ketjen black-modified water proof carbon paper (KB/WPCC) was used as an electrode material. The KB/WPCC surface was modified with 2-aminobenzoic acid and p-phenylenediamine, respectively, to face the positively charged electron-accepting site of BOD and the negatively charged electron-donating site of MBH to the electrode surface. A gas-diffusion system was employed for the electrodes to realize high-speed substrate supply. As result, great improvement in the current density of O2 reduction with BOD and H2 reduction with MBH were realized at negatively and postively charged surfaces, respectively. Gas diffusion system also suppressed the oxidative inactivation of MBH at high electrode potentials. Finally, based on the improved bioanode and biocathode, a dual gas-diffusion membrane- and mediatorless H2/air-breathing biofuel cell was constructed. The maximum power density reached 6.1 mW cm-2 (at 0.72 V), and the open circuit voltage was 1.12 V using 1 atm of H2 gas as a fuel at room temperature and under passive and quiescent conditions.

  13. Radiochemical studies on amorphous zirconium phosphate

    Energy Technology Data Exchange (ETDEWEB)

    Dyer, A; Moores, G E [Salford Univ. (UK). Dept. of Chemistry and Applied Chemistry

    1981-01-01

    Amorphous zirconium phosphate (ZrP) is used in some hemodialysis machines for the regeneration of dialysate. Its function is to adsorb ammonium ions formed by the pretreatment of urea by urease. It also adsorbs Ca, Mg and K ions but leaches phosphate ions which are then removed (along with F/sup -/ ions) by a bed of hydrous zirconium oxide. The sodium form of ZrP is used although other forms have been suggested for use. The work reported here describes some preliminary radiochemical studies on the mechanism of release of phosphate ions and its possible relationship to sodium ion-exchange. /sup 32/P labelled material (HHZrP) was used for elution experiments with deionized water and buffer solutions having the pH's 4.2, 7.0 and 9.2. Buffer solutions used were as supplied by BDH. Elution was at four different temperatures in the range 293 to 363/sup 0/C. In the second series of experiments HHZrP was suspended in a NaCl solution labelled with /sup 22/Na. From this, /sup 22/Na labelled ZrP (NaHZrP) was prepared and eluted in the same way as the HHZrP. Results are given and discussed.

  14. Process for obtaining ammonium uranyl tri carbonate

    International Nuclear Information System (INIS)

    Santos, L.R. dos; Riella, H.G.

    1992-01-01

    The procedure adopted for obtaining Ammonium Uranyl Carbonate (AUC) from uranium hexafluoride (U F 6 ) in a aqueous solutions of ammonium hydrogen carbonate is described in this work. The precipitation is made in temperature and pH controlled. This process consists of three steps: evaporation of U F 6 , AUC precipitation and filtration of the AUC slurry. An attempt is made of correlate the parameters involved in the precipitation process of AUC with its and U O 2 characteristics. (author)

  15. Stabilization of Pb(II) accumulated in biomass through phosphate-pretreated pyrolysis at low temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Li, Saijun; Zhang, Tao; Li, Jianfa, E-mail: ljf@usx.edu.cn; Shi, Lingna; Zhu, Xiaoxiao; Lü, Jinhong; Li, Yimin

    2017-02-15

    Highlights: • Phosphate-pretreated pyrolysis can stabilize Pb(II) accumulated in biomass. • More than 95% of Pb(II) in celery and wood biomass was stabilized. • Pb from biomass was almost totally retained in char. • Most Pb was transformed into phosphates according to XRD and SEM/EDX analyses. - Abstract: The remediation of heavy metal-contaminated soil and water using plant biomass is considered to be a green technological approach, although the harmless disposal of biomass accumulated with heavy metals remains a challenge. A potential solution to this problem explored in this work involves combining phosphate pretreatment with pyrolysis. Pb(II) was accumulated in celery biomass with superior sorption capacity and also in ordinary wood biomass through biosorption. The Pb(II)-impregnated biomass was then pretreated with phosphoric acid or calcium dihydrogen phosphate (CaP) and pyrolyzed at 350 or 450 °C. Pb(II) from biomass was in turn almost totally retained in chars, and the percentage of DTPA-extractable Pb(II) was reduced to less than 5% of total Pb(II) in chars through CaP pretreatment. Pb(II) stabilization was further confirmed through a sequential extraction test, which showed that more than 95% of Pb(II) was converted into stable species composed mainly of lead phosphates according to X-ray diffraction (XRD) and scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDX) analyses. Overall, phosphate-pretreated pyrolysis can stabilize both Pb(II) and degradable biomass, so as to control efficiently the hazards of heavy metal-contaminated biomass.

  16. Quantum dynamics through a wave packet method to study electron-hydrogen and atom-dihydrogen collisions; Dynamique quantique par une methode de paquets d'ondes. Etude des collisions electron-hydrogene et atome-dihydrogene

    Energy Technology Data Exchange (ETDEWEB)

    Mouret, L

    2002-11-01

    The thesis concerns the development and implementation of numerical methods for solving the time-dependent Schroedinger equation. We first considered the case of electron-hydrogen scattering. The originality of our method is the use of a non-uniform radial grid defined by a Schwarz interpolation based on a Coulomb reference function. This grid allows many hydrogen bound states and associated matrix elements of various operators to be reproduced to machine accuracy. The wave function is propagated in time using a Split-Operator method. The efficiency of our method allows the wave function to be propagated out to large distances for all partial waves. We obtain excitation and ionization cross sections in excellent agreement with the best experimental and theoretical data. We subsequently adapted the method and the program package to study reactive atom-dihydrogen scattering. The wave packet is described using product Jacobi coordinates on a regular grid of radial coordinates combined with a basis of Legendre polynomials for the angular part (partial wave S). The wave function is analysed using a time-to-energy Fourier transform, which provides results over the energy range covered by the initial wave packet in one calculation. The method was first tested on the quasi-direct (F,H2) reaction and then applied to the indirect (C(1D),H2)reaction. The state-to-state reaction probabilities are in good agreement with those obtained by a time-independent approach. In particular, the strongly resonant structure of the (C(1D),H2) reaction probabilities is well reproduced. (author)

  17. Quantum dynamics through a wave packet method to study electron-hydrogen and atom-dihydrogen collisions; Dynamique quantique par une methode de paquets d'ondes. Etude des collisions electron-hydrogene et atome-dihydrogene

    Energy Technology Data Exchange (ETDEWEB)

    Mouret, L

    2002-11-01

    The thesis concerns the development and implementation of numerical methods for solving the time-dependent Schroedinger equation. We first considered the case of electron-hydrogen scattering. The originality of our method is the use of a non-uniform radial grid defined by a Schwarz interpolation based on a Coulomb reference function. This grid allows many hydrogen bound states and associated matrix elements of various operators to be reproduced to machine accuracy. The wave function is propagated in time using a Split-Operator method. The efficiency of our method allows the wave function to be propagated out to large distances for all partial waves. We obtain excitation and ionization cross sections in excellent agreement with the best experimental and theoretical data. We subsequently adapted the method and the program package to study reactive atom-dihydrogen scattering. The wave packet is described using product Jacobi coordinates on a regular grid of radial coordinates combined with a basis of Legendre polynomials for the angular part (partial wave S). The wave function is analysed using a time-to-energy Fourier transform, which provides results over the energy range covered by the initial wave packet in one calculation. The method was first tested on the quasi-direct (F,H2) reaction and then applied to the indirect (C(1D),H2)reaction. The state-to-state reaction probabilities are in good agreement with those obtained by a time-independent approach. In particular, the strongly resonant structure of the (C(1D),H2) reaction probabilities is well reproduced. (author)

  18. Crystallization characteristics of ammonium uranyl carbonate (AUC) in ammonium carbonate solutions

    International Nuclear Information System (INIS)

    Kim, T.J.; Jeong, K.C.; Park, J.H.; Chang, I.S.; Choi, C.S.

    1994-01-01

    Ammonium carbonate solutions with an excessive amount of NH 3 were produced in a commercial AUC (ammonium uranyl carbonate) conversion plant. In this study the AUC crystals, precipitated with uranyl nitrate and ammonium carbonate solutions prepared in the laboratory, were characterized to determine the feasibility of recycling ammonium carbonate solution. The AUC crystals were easily agglomerated with the increasing concentration of CO 3 2- and mole ratio of NH 4 + /CO 3 2- in ammonium carbonate solution. Effects of a mixing system for the solution in the AUC crystallizer and the feed location of the solution onthe agglomeration of AUC crystals were also studied along with the effects of agglomerated AUC powders on UO 2 powders. Finally, the feasibility of manufacturing UO 2 fuel with a sintered pellet density of 10.52 g/cm 3 , using the AUC powders generated in this experiment, was demonstrated. (orig.)

  19. Performance of flexible capacitors based on polypyrrole/carbon fiber electrochemically prepared from various phosphate electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Yuan, Wei; Han, Gaoyi, E-mail: han_gaoyis@sxu.edu.cn; Chang, Yunzhen; Li, Miaoyu; Xiao, Yaoming, E-mail: ymxiao@sxu.edu.cn; Zhou, Haihan; Zhang, Ying; Li, Yanping

    2016-11-30

    Highlights: • PPy/CFs have been fabricated by electrodepositing polypyrrole on carbon fibers. • The electrolytes in deposition solution have effect on PPy/CFs’ capacitive behavior. • Cells of PPy/CFs obtained from NaH{sub 2}PO{sub 4} electrolyte has good stability in PVA/H{sub 3}PO{sub 4}. - Abstract: In order to investigate the influence of electrolytes in electro-deposition solution on the capacitive properties of polypyrrole (PPy), we have chosen phosphoric acid, phosphate, hydrogen phosphate and dihydrogen phosphate as electrolyte in deposition solution respectively and electrochemically deposited PPy on carbon fibers (CFs) via galvanostatic method. The morphologies of the PPy/CFs samples have been characterized by scanning electron microscope. The specific capacitance of PPy/CFs samples has been evaluated in different electrolytes through three-electrode test system. The assembled flexible capacitors by using PPy/CFs as electrodes and H{sub 3}PO{sub 4}/polyvinyl alcohol as gel electrolyte have been systematically measured by cyclic voltammetry, galvanostatic charge/discharge and electrochemical impedance spectroscopy. The results show that the electrochemical capacitors based on PPy/CFs prepared from deposition solution containing NaH{sub 2}PO{sub 4}·2H{sub 2}O electrolyte exhibit higher specific capacitance, flexibility and excellent stability (retaining 96.8% of initial capacitance after 13,000 cycles), and that three cells connected in series can power a light-emitting diode.

  20. The analysis of impurities in the diuranate-determination of phosphate by phosphomolybdate blue spectrophotometric method

    International Nuclear Information System (INIS)

    Sun Haobo

    2014-01-01

    Phosphomolybdenum blue spectrophotometric method was used for determination of phosphate in the diuranate. Diuranate was dissolved in nitric acid solution, in which formed a soluble heteropolyacid complex (namely phosphomolybdenum yellow) due to interaction of phosphate and ammonium molybdate. Then phosphomolybdenum yellow was reduced to phosphomolybdenum blue with Bismuth nitrate as catalyst. Colour intensity at 700 nm is in proportion to the content of phosphate determined by spectrophotometric method. This experiment presents good linearity at the range of 30 μg to 245 μg phosphate, and the relative standard deviation of the experimental result is 2.4%, and the recovery rate is from 95% to 105%. The determination result of phosphate content will not be effected under conditions of 4 mg of SiO 2 , 6 mg of Fe, 400 mg of Cl - and 4.5 mg of Ge in the solution. (author)

  1. High-precision determination of 18O/16O ratios of silver phosphate by EA-pyrolysis-IRMS continuous flow technique.

    Science.gov (United States)

    Lécuyer, Christophe; Fourel, François; Martineau, François; Amiot, Romain; Bernard, Aurélien; Daux, Valérie; Escarguel, Gilles; Morrison, John

    2007-01-01

    A high-precision, and rapid on-line method for oxygen isotope analysis of silver phosphate is presented. The technique uses high-temperature elemental analyzer (EA)-pyrolysis interfaced in continuous flow (CF) mode to an isotopic ratio mass spectrometer (IRMS). Calibration curves were generated by synthesizing silver phosphate with a 13 per thousand spread in delta(18)O values. Calibration materials were obtained by reacting dissolved potassium dihydrogen phosphate (KH(2)PO(4)) with water samples of various oxygen isotope compositions at 373 K. Validity of the method was tested by comparing the on-line results with those obtained by classical off-line sample preparation and dual inlet isotope measurement. In addition, silver phosphate precipitates were prepared from a collection of biogenic apatites with known delta(18)O values ranging from 12.8 to 29.9 per thousand (V-SMOW). Reproducibility of +/- 0.2 per thousand was obtained by the EA-Py-CF-IRMS method for sample sizes in the range 400-500 microg. Both natural and synthetic samples are remarkably well correlated with conventional (18)O/(16)O determinations. Silver phosphate is a very stable material and easy to degas and, thus, could be considered as a good candidate to become a reference material for the determination of (18)O/(16)O ratios of phosphate by high-temperature pyrolysis. Copyright 2006 John Wiley & Sons, Ltd.

  2. Mechanistic aspects of dinitrogen cleavage and hydrogenation to produce ammonia in catalysis and organometallic chemistry: relevance of metal hydride bonds and dihydrogen.

    Science.gov (United States)

    Jia, Hong-Peng; Quadrelli, Elsje Alessandra

    2014-01-21

    Dinitrogen cleavage and hydrogenation by transition-metal centers to produce ammonia is central in industry and in Nature. After an introductory section on the thermodynamic and kinetic challenges linked to N2 splitting, this tutorial review discusses three major classes of transition-metal systems (homogeneous, heterogeneous and biological) capable of achieving dissociation and hydrogenation of dinitrogen. Molecular complexes, solid-state Haber-Bosch catalytic systems, silica-supported tantalum hydrides and nitrogenase will be discussed. Emphasis is focused on the reaction mechanisms operating in the process of dissociation and hydrogenation of dinitrogen, and in particular on the key role played by metal hydride bonds and by dihydrogen in such reactions.

  3. Reaction of ammonium triphosphate with gadolinium nitrate in aqueous solution at 273K

    International Nuclear Information System (INIS)

    Rodicheva, G.V.; Tananaev, I.V.; Romanova, N.M.

    1982-01-01

    The solubility in the system (NW 4 ) 5 P 3 O 10 -Gd(NO 3 ) 3 - H 2 O (273 K) is studied. Depending on the reagent ratio formation of the compounds Gd 5 (P 3 O 10 ) 3 x22H 2 O, NH 4 Gd 3 (P 3 O 10 ) 2 x12H 2 O and (NH 4 ) 3 Gd 4 (P 3 O 10 ) 3 x14H 2 O is established. Gadolinium triphosphates, separated from solution, are studied using the methods of paper chromatography, X-ray diffractometry, thermography. Simultaneously with thermal dehydration of gadolinium triphosphates the processes of triphosphate decomposition and phosphate anion condensation take place. A mixture of crystalline ortho-phosphate and long- chain polyphosphate of gadolinium is the final product of thermal decomposition (1063 K) of normal and doubl e ammonium- containing gadolinium triphosphates [ru

  4. Growth of single crystals from solutions using semi-permeable membranes

    Science.gov (United States)

    Varkey, A. J.; Okeke, C. E.

    1983-05-01

    A technique suitable for growth of single crystals from solutions using semi-preamble membranes is described. Using this technique single crystals of copper sulphate, potassium bromide and ammonium dihydrogen phosphate have been successfully grown. Advantages of this technique over other methods are discussed.

  5. Effects of Aromatic Ammoniums on Methyl Ammonium Lead Iodide Hybrid Perovskite Materials

    Directory of Open Access Journals (Sweden)

    Jianli Yang

    2017-01-01

    Full Text Available The introduction of bulky ammoniums into methyl ammonium lead iodide hybrid perovskites (MAPbI3 has emerged as a promising strategy to improve the properties of these materials. In the present work, we studied the effects of several aromatic ammoniums onto the structural, electronic, and optical properties of MAPbI3. Although powder XRD data suggest that the bulky cations are not involved in the bulk phase of the MAPbI3, a surprisingly large effect of the bulky cations onto the photoluminescence properties was observed.

  6. Evidence of ammonium ion-exchange properties of natural bentonite and application to ammonium detection.

    Science.gov (United States)

    Zazoua, A; Kazane, I; Khedimallah, N; Dernane, C; Errachid, A; Jaffrezic-Renault, N

    2013-12-01

    Ammonium exchange with hybrid PVC-bentonite (mineral montmorillonite clay) thin film was revealed using FTIR spectroscopy, EDX, cyclic voltammetry and electrochemical impedance spectroscopy. The effect of ammonium exchange on the charge transfer resistance of PVC-bentonite hybrid thin film was attributed to a modification of the intersheet distance and hydration of bentonite crystals. The obtained impedimetric ammonium sensor shows a linear range of detection from 10(-4)M to 1M and a detection limit around 10(-6)M. © 2013.

  7. Partitioning of L-methionine in aqueous two-phase systems containing poly(propylene glycol) and sodium phosphate salts

    Energy Technology Data Exchange (ETDEWEB)

    Salabat, Alireza, E-mail: a-salabat@araku.ac.ir [Chemistry Department, Arak University, P.O. Box 38156-879, Arak (Iran, Islamic Republic of); Sadeghi, Rahmat [Department of Chemistry, University of Kurdistan, Sanandaj, Kurdistan 66135 (Iran, Islamic Republic of); Moghadam, Somayeh Tiani [Chemistry Department, Arak University, P.O. Box 38156-879, Arak (Iran, Islamic Republic of); Jamehbozorg, Bahman [Department of Chemistry, University of Kurdistan, Sanandaj, Kurdistan 66135 (Iran, Islamic Republic of)

    2011-10-15

    Highlights: > Thermodynamics parameters for partitioning of L-methionine in ATPS. > Investigation of different effects on partition coefficient of the amino acid. > Propose the best condition for L-methionine partitioning. - Abstract: The partitioning behavior of L-methionine has been studied in aqueous two-phase systems of (poly(propylene glycol) + sodium phosphate salts + H{sub 2}O) at different temperatures. The salts used were sodium di-hydrogen phosphate (NaH{sub 2}PO{sub 4}), di-sodium hydrogen phosphate (Na{sub 2}HPO{sub 4}) and tri-sodium phosphate (Na{sub 3}PO{sub 4}). The effects of tie line length, salt type, and temperature on the partition coefficient of this amino acid have been studied. In addition, thermodynamic parameters ({Delta}H{sup o}, {Delta}S{sup o} and {Delta}G{sup o}) as a function of temperature were calculated. The results showed that increasing tie line length led to decreasing of the partition coefficient. We also showed that the partition coefficients of the amino acid in the systems containing Na{sub 3}PO{sub 4} are greater than the other two salts. Moreover, it is verified that increasing temperature led to decreasing the partition coefficient. The experimental partition coefficient data are correlated using a modified virial-type model.

  8. Partitioning of L-methionine in aqueous two-phase systems containing poly(propylene glycol) and sodium phosphate salts

    International Nuclear Information System (INIS)

    Salabat, Alireza; Sadeghi, Rahmat; Moghadam, Somayeh Tiani; Jamehbozorg, Bahman

    2011-01-01

    Highlights: → Thermodynamics parameters for partitioning of L-methionine in ATPS. → Investigation of different effects on partition coefficient of the amino acid. → Propose the best condition for L-methionine partitioning. - Abstract: The partitioning behavior of L-methionine has been studied in aqueous two-phase systems of (poly(propylene glycol) + sodium phosphate salts + H 2 O) at different temperatures. The salts used were sodium di-hydrogen phosphate (NaH 2 PO 4 ), di-sodium hydrogen phosphate (Na 2 HPO 4 ) and tri-sodium phosphate (Na 3 PO 4 ). The effects of tie line length, salt type, and temperature on the partition coefficient of this amino acid have been studied. In addition, thermodynamic parameters (ΔH o , ΔS o and ΔG o ) as a function of temperature were calculated. The results showed that increasing tie line length led to decreasing of the partition coefficient. We also showed that the partition coefficients of the amino acid in the systems containing Na 3 PO 4 are greater than the other two salts. Moreover, it is verified that increasing temperature led to decreasing the partition coefficient. The experimental partition coefficient data are correlated using a modified virial-type model.

  9. Effect of Ethylenediaminetetraacetic Acid and Ammonium Oxalate ...

    African Journals Online (AJOL)

    Effect of Ethylenediaminetetraacetic Acid and Ammonium Oxalate on the ... The test plant was sown in aluminium-polluted soil (conc. ... The perseverance of the test plant in the aluminium spiked soil is an indication of adaptation to the stress ...

  10. Optimization of nutritional requirements and ammonium feeding ...

    African Journals Online (AJOL)

    Statistical experiment design and data analysis were used to establish the major factors in a chemically defined medium and to develop an ammonium control strategy to optimize the specific vitamin B12 production rate (Yp) of Pseudomonas denitrificans. Through Plackett-Burman design, the major factors of glucose, ...

  11. 21 CFR 184.1135 - Ammonium bicarbonate.

    Science.gov (United States)

    2010-04-01

    ... 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) FOOD FOR HUMAN CONSUMPTION (CONTINUED) DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of Specific Substances Affirmed as GRAS § 18...

  12. Ammonium ions determination with polypyrrole modified electrode

    Directory of Open Access Journals (Sweden)

    Luiz Henrique Dall´Antonia

    2007-03-01

    Full Text Available The present work relates the preparation of polypyrrole films (PPy deposited on surfaces of glass carbon, nickel and ITO (tin oxide doped with indium on PET plastic, in order to study the ammonium detection. The popypyrrole films were polymerized with dodecylbenzenesulfonate (DBSA on the electrodes, at + 0,70 V vs. Ag/AgCl, based on a solution containing the pyrrole monomer and the amphiphilic salt. Films deposited on glass carbon presented better performance. Cyclic voltammetries, between – 1,50 to + 0,5 V vs. Ag/AgCl, were repeated adding different concentrations of NH4Cl, in order to observe the behavior of the film as a possible detector of ions NH4+. The peak current for oxidation varies with the concentration of ammonium. A linear region can be observed in the band of 0 to 80 mM, with a sensibility (Sppy approximately similar to 4,2 mA mM-1 cm-2, showing the efficacy of the electrodes as sensors of ammonium ions. The amount of deposited polymer, controlled by the time of growth, does not influence on the sensor sensibility. The modified electrode was used to determine ammonium in grounded waters.

  13. 21 CFR 558.340 - Maduramicin ammonium.

    Science.gov (United States)

    2010-04-01

    .... Feed continuously as sole ration. Do not feed to laying hens. Withdraw 5 days before slaughter. (2... DRUGS, FEEDS, AND RELATED PRODUCTS NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS Specific New Animal Drugs for Use in Animal Feeds § 558.340 Maduramicin ammonium. (a) Approvals. Type A medicated articles: 4.54...

  14. Anaerobic oxidation of methane and ammonium.

    NARCIS (Netherlands)

    Strous, M.; Jetten, M.S.M.

    2004-01-01

    Anaerobic oxidation of methane and ammonium are two different processes catalyzed by completely unrelated microorganisms. Still, the two processes do have many interesting aspects in common. First, both of them were once deemed biochemically impossible and nonexistent in nature, but have now been

  15. Near infrared detection of ammonium minerals.

    Science.gov (United States)

    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

  16. Effect of Ethylenediaminetetraacetic Acid and Ammonium Oxalate ...

    African Journals Online (AJOL)

    ADOWIE PERE

    acid and ammonium oxalate on the prevalence of microorganisms and removal of aluminum in soil by bitter leaf plant (Vernonia ... highest accumulation of aluminium in the root (16.92mg/kg); however concentrations of aluminium in the roots were .... whereas the sulphate was 13.75mg/kg. Table 2: The total colony count of ...

  17. Detonation characteristics of ammonium nitrate products

    NARCIS (Netherlands)

    Kersten, R.J.A.; Hengel, E.I.V. van den; Steen, A.C. van der

    2006-01-01

    The detonation properties of ammonium nitrate (AN) products depend on many factors and are therefore, despite the large amount of information on this topic, difficult to assess. In order to further improve the understanding of the safety properties of AN, the European Fertilizer Manufacturers

  18. Alanine synthesis from glyceraldehyde and ammonium ion in aqueous solution

    Science.gov (United States)

    Weber, A. L.

    1985-01-01

    The formation of alanine (ala) form C(14)-glyceraldehyde and ammonium phosphate in the presence or absence of a thiol is reported. At ambient temperature, ala synthesis was six times more rapid in the presence of 3-mercaptopropionic acid than in its absence (0.6 and 0.1 percent, respectively, after 60 days). Similarly, the presence of another thiol, N-acetylcysteinate, increased the production of ala, as well as of lactate. The reaction pathway of thiol-catalyzed synthesis of ala, with the lactic acid formed in a bypath, is suggested. In this, dehydration of glyceraldehyde is followed by the formation of hemithioacetal. In the presence of ammonia, an imine is formed, which eventually yields ala. This pathway is consistent with the observation that the rate ratio of ala/lactate remains constant throughout the process. The fact that the reaction takes place under anaerobic conditions in the presence of H2O and with the low concentrations of simple substrates and catalysts makes it an attractive model prebiotic reaction in the process of molecular evolution.

  19. Phosphate control in dialysis

    Directory of Open Access Journals (Sweden)

    Cupisti A

    2013-10-01

    Full Text Available Adamasco Cupisti,1 Maurizio Gallieni,2 Maria Antonietta Rizzo,2 Stefania Caria,3 Mario Meola,4 Piergiorgio Bolasco31Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy; 2Nephrology and Dialysis Unit, San Carlo Borromeo Hospital, Milan, Italy; 3Territorial Department of Nephrology and Dialysis, ASL Cagliari, Italy; 4Sant'Anna School of Advanced Studies, University of Pisa, Pisa, ItalyAbstract: Prevention and correction of hyperphosphatemia is a major goal of chronic kidney disease–mineral and bone disorder (CKD–MBD management, achievable through avoidance of a positive phosphate balance. To this aim, optimal dialysis removal, careful use of phosphate binders, and dietary phosphate control are needed to optimize the control of phosphate balance in well-nourished patients on a standard three-times-a-week hemodialysis schedule. Using a mixed diffusive–convective hemodialysis tecniques, and increasing the number and/or the duration of dialysis tecniques are all measures able to enhance phosphorus (P mass removal through dialysis. However, dialytic removal does not equal the high P intake linked to the high dietary protein requirement of dialysis patients; hence, the use of intestinal P binders is mandatory to reduce P net intestinal absorption. Unfortunately, even a large dose of P binders is able to bind approximately 200–300 mg of P on a daily basis, so it is evident that their efficacy is limited in the case of an uncontrolled dietary P load. Hence, limitation of dietary P intake is needed to reach the goal of neutral phosphate balance in dialysis, coupled to an adequate protein intake. To this aim, patients should be informed and educated to avoid foods that are naturally rich in phosphate and also processed food with P-containing preservatives. In addition, patients should preferentially choose food with a low P-to-protein ratio. For example, patients could choose egg white or protein from a vegetable source

  20. Uranium production from phosphates

    International Nuclear Information System (INIS)

    Ketzinel, Z.; Folkman, Y.

    1979-05-01

    According to estimates of the world's uranium consumption, exploitation of most rich sources is expected by the 1980's. Forecasts show that the rate of uranium consumption will increase towards the end of the century. It is therefore desirable to exploit poor sources not yet in use. In the near future, the most reasonable source for developing uranium is phosphate rock. Uranium reserves in phosphates are estimated at a few million tons. Production of uranium from phosphates is as a by-product of phosphate rock processing and phosphoric acid production; it will then be possible to save the costs incurred in crushing and dissolving the rock when calculating uranium production costs. Estimates show that the U.S. wastes about 3,000 tons of uranium per annum in phosphoric acid based fertilisers. Studies have also been carried out in France, Yugoslavia and India. In Israel, during the 1950's, a small plant was operated in Haifa by 'Chemical and Phosphates'. Uranium processes have also been developed by linking with the extraction processes at Arad. Currently there is almost no activity on this subject because there are no large phosphoric acid plants which would enable production to take place on a reasonable scale. Discussions are taking place about the installation of a plant for phosphoric acid production utilising the 'wet process', producing 200 to 250,000 tons P 2 O 5 per annum. It is necessary to combine these facilities with uranium production plant. (author)

  1. PRN 88-2: Clustering of Quaternary Ammonium Compounds

    Science.gov (United States)

    This Notice announces that EPA has clustered the Quaternary Ammonium Compounds into four groups for the purpose of testing chemicals to build a database that will support continued registration of the entire family of quaternary ammonium compounds

  2. 40 CFR 180.473 - Glufosinate ammonium; tolerances for residues.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 23 2010-07-01 2010-07-01 false Glufosinate ammonium; tolerances for... § 180.473 Glufosinate ammonium; tolerances for residues. (a) General. Tolerances are established for residues of the herbicide glufosinate-ammonium (butanoic acid, 2-amino-4-(hydroxymethylphosphinyl...

  3. Spectrometric determination of ammonium-nitrogen with quinol in ...

    African Journals Online (AJOL)

    Quinol is proposed as a reagent for the spectrometric determination of ammonium-nitrogen (NH4+-N) in aqueous medium. Quinol forms a pink complex with ammonium salt in aqueous medium. Hydrogen peroxide is needed for colour accentuation. The quinol/ammonium charge transfer complex has absorption maximum ...

  4. The Australian national reactive phosphate rock project - Aims, experimental approach, and site characteristics

    International Nuclear Information System (INIS)

    McLaughlin, M.J.

    2002-01-01

    Field-based cutting trials were established across Australia in a range of environments to evaluate the agronomic effectiveness of 5 phosphate rocks, and 1 partially acidulated phosphate rock, relative to either single super-phosphate or triple superphosphate. The phosphate rocks differed in reactivity, as determined by the degree of carbonate substitution for phosphate in the apatite structure and solubility of phosphorus present in the fertilizers in 2% formic acid, 2% citric acid and neutral ammonium citrate. Sechura (Bayovar) and North Carolina phosphate rocks were highly reactive (>70% solubility in 2% formic acid), whilst Khouribja (Moroccan) and Hamrawein (Egypt) phosphate rock were moderately reactive. Duchess phosphate rock from Queensland was relatively unreactive ( 2 , from 4.0 to 5.1, and Colwell extractable phosphorus ranged from 3 to 47 μg/g prior to fertilizer application. Two core experiments were established at each site. The first measured the effects of phosphate rock reactivity on agronomic effectiveness, while the second core experiment measured the effects of the degree of water solubility of the phosphorus source on agronomic effectiveness. The National Reactive Phosphate Rock Project trials provided the opportunity to confirm the suitability of accepted procedures to model fertilizer response and to develop new approaches for comparing different fertilizer responses. The Project also provided the framework for subsidiary studies such as the effect of fertilizer source on soil phosphorus extractability; cadmium and fluorine concentrations in herbage; evaluation of soil phosphorus tests; and the influence of particle size on phosphate rock effectiveness. The National Reactive Phosphate Rock Project presents a valuable model for a large, Australia-wide, collaborative team approach to an important agricultural issue. The use of standard and consistent experimental methodologies at every site ensured that maximum benefit was obtained from data

  5. Effect of sodium phosphate salts on the thermodynamic properties of aqueous solutions of poly(ethylene oxide) 6000 at different temperatures

    International Nuclear Information System (INIS)

    Sadeghi, Rahmat; Hosseini, Rahim; Jamehbozorg, Bahman

    2008-01-01

    Precise density, sound velocity, water activity, and phase diagram measurements have been carried out on polyethylene oxide (PEO) in aqueous solutions of sodium di-hydrogen phosphate, di-sodium hydrogen phosphate, and tri-sodium phosphate over a range of temperatures at atmospheric pressure. The experimental density and sound velocity data are used to calculate the apparent specific volume and isentropic compressibility as a function of temperature and concentration. It was found that both of the apparent specific volume and isentropic compressibility of PEO in aqueous solutions increase by increasing temperature and charge on the anion of electrolytes. The results show that the slope of constant water activity lines increased with increasing the temperature and charge on the anion of electrolytes and the vapour pressure depression for an aqueous (PEO + sodium phosphate) system is more than the sum of those for the corresponding binary solutions. Furthermore, the effect of temperature and type of anion of salt on the salting-out effect of polyethylene oxide by sodium phosphate salts has been studied

  6. Effect of sodium phosphate salts on the thermodynamic properties of aqueous solutions of poly(ethylene oxide) 6000 at different temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Sadeghi, Rahmat [Department of Chemistry, University of Kurdistan, Sanandaj (Iran, Islamic Republic of)], E-mail: rahsadeghi@yahoo.com; Hosseini, Rahim; Jamehbozorg, Bahman [Department of Chemistry, University of Kurdistan, Sanandaj (Iran, Islamic Republic of)

    2008-09-15

    Precise density, sound velocity, water activity, and phase diagram measurements have been carried out on polyethylene oxide (PEO) in aqueous solutions of sodium di-hydrogen phosphate, di-sodium hydrogen phosphate, and tri-sodium phosphate over a range of temperatures at atmospheric pressure. The experimental density and sound velocity data are used to calculate the apparent specific volume and isentropic compressibility as a function of temperature and concentration. It was found that both of the apparent specific volume and isentropic compressibility of PEO in aqueous solutions increase by increasing temperature and charge on the anion of electrolytes. The results show that the slope of constant water activity lines increased with increasing the temperature and charge on the anion of electrolytes and the vapour pressure depression for an aqueous (PEO + sodium phosphate) system is more than the sum of those for the corresponding binary solutions. Furthermore, the effect of temperature and type of anion of salt on the salting-out effect of polyethylene oxide by sodium phosphate salts has been studied.

  7. Recovering uranium from phosphates

    Energy Technology Data Exchange (ETDEWEB)

    Bergeret, M [Compagnie de Produits Chimiques et Electrometallurgiques Pechiney-Ugine Kuhlmann, 75 - Paris (France)

    1981-06-01

    Processes for the recovery of the uranium contained in phosphates have today become competitive with traditional methods of working uranium sources. These new possibilities will make it possible to meet more rapidly any increases in the demand for uranium: it takes ten years to start working a new uranium deposit, but only two years to build a recovery plant.

  8. Thermophysical properties of hydroxyl ammonium ionic liquids

    International Nuclear Information System (INIS)

    Kurnia, K.A.; Wilfred, C.D.; Murugesan, T.

    2009-01-01

    The thermophysical properties of hydroxyl ammonium ionic liquids: density ρ, T = (293.15 to 363.15) K; dynamic viscosity η, T = (298.2 to 348.2) K; and refractive indices n D , T = (293.15 to 333.15) K have been measured. The coefficients of thermal expansion α, values were calculated from the experimental density results using an empirical correlation for T = (293.15 to 363.15) K. The variation of volume expansion of ionic liquids studied was found to be independent of temperature within the range covered in the present work. The thermal decomposition temperature 'T d ' for all the six hydroxyl ammonium ionic liquids is also investigated using thermogravimetric analyzer (TGA)

  9. Quaternary ammonium compounds – New occupational hazards

    Directory of Open Access Journals (Sweden)

    Agnieszka Lipińska-Ojrzanowska

    2014-10-01

    Full Text Available Quaternary ammonium compounds (QACs, quats belong to organic ionic chemical agents which display unique properties of both surfactants and disinfectants. Their wide distribution in the work environment and also in private households brings about new occupational hazards. This paper reviews reports about the health effects of QACs. QACs could play a role of sensitizers and irritants to the skin and mucous membranes. It is suspected that particular QACs can display an immunologic crossreactivity between each other and with other chemical compounds containing ammonium ion, such as muscle relaxants widely used in anesthesia. They may promote the development of airway allergy, however, the background mechanisms are still unclear and need to be further investigated. Until now, a few cases of occupational asthma induced by QACs have been described and their involvement in contact dermatitis has been documented. The possibility of anaphylaxis due to QACs cannot be excluded as well. Med Pr 2014;65(5:675–682

  10. Development of technology for ammonium nitrate dissociation process

    International Nuclear Information System (INIS)

    Zakharkin, B.S.; Varykhanov, V.P.; Kucherenko, V.S.; Solov'yeva, L.N.; Revyakin, V.V.

    2000-01-01

    Ammonia and ammonium carbonate are frequently used as reagents in fuel production and processing of liquid radioactive wastes. In particular, liquid radioactive wastes that contain ammonium nitrate are generated during operations of metal precipitation. In closed vessels at elevated temperature, for example in evaporators or deposits in tubing, ammonium nitrate may explode due to generation of gaseous nitrogen oxides [2]. In this connection, steps have to be taken to rule out conditions that result in explosion. To do that, ammonium nitrate should be removed even prior to the initial stage of its formation. This report gives results of development of a method of dissociating ammonium nitrate

  11. Decomposition of ammonium nitrate in homogeneous and catalytic denitration

    International Nuclear Information System (INIS)

    Anan'ev, A. V.; Tananaev, I. G.; Shilov, V. P.

    2005-01-01

    Ammonium nitrate is one of potentially explosive by-products of spent fuel reprocessing. Decomposition of ammonium nitrate in the HNO 3 -HCOOH system was studied in the presence or absence of Pt/SiO 2 catalyst. It was found that decomposition of ammonium nitrate is due to homogeneous noncatalytic oxidation of ammonium ion with nitrous acid generated in the HNO 3 -HCOOH system during denitration. The platinum catalyst initiates the reaction of HNO 3 with HCOOH to form HNO 2 . The regular trends were revealed and the optimal conditions of decomposition of ammonium nitrate in nitric acid solutions were found [ru

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

    Science.gov (United States)

    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.

  13. Review on Thermal Decomposition of Ammonium Nitrate

    Science.gov (United States)

    Chaturvedi, Shalini; Dave, Pragnesh N.

    2013-01-01

    In this review data from the literature on thermal decomposition of ammonium nitrate (AN) and the effect of additives to their thermal decomposition are summarized. The effect of additives like oxides, cations, inorganic acids, organic compounds, phase-stablized CuO, etc., is discussed. The effect of an additive mainly occurs at the exothermic peak of pure AN in a temperature range of 200°C to 140°C.

  14. Thermal decomposition kinetics of ammonium uranyl carbonate

    International Nuclear Information System (INIS)

    Kim, E.H.; Park, J.J.; Park, J.H.; Chang, I.S.; Choi, C.S.; Kim, S.D.

    1994-01-01

    The thermal decomposition kinetics of AUC [ammonium uranyl carbonate; (NH 4 ) 4 UO 2 (CO 3 ) 3 [ in an isothermal thermogravimetric (TG) reactor under N 2 atmosphere has been determined. The kinetic data can be represented by the two-dimensional nucleation and growth model. The reaction rate increases and activation energy decreases with increasing particle size and precipitation time which appears in the particle size larger than 30 μm in the mechano-chemical phenomena. (orig.)

  15. 21 CFR 184.1133 - Ammonium alginate.

    Science.gov (United States)

    2010-04-01

    ...: Category of food Maximum level of use in food (as served) (percent) Functional use Confections, frostings... chapter 0.4 Do. Sweet sauces, § 170.3(n)(43) of this chapter 0.5 Do. All other food categories 0.1... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ammonium alginate. 184.1133 Section 184.1133 Food...

  16. Standard characterization of phosphate rock samples from the FAO/IAEA phosphate project

    International Nuclear Information System (INIS)

    Binh, Truong; Zapata, F.

    2002-01-01

    Phosphate rocks (PR) are phosphate-bearing minerals that vary widely in their inherent characteristics and consequently their agronomic potential. In the framework of a FAO/IAEA networked research project, the evaluation of the agronomic effectiveness of natural and modified PR products under a variety of soil climate and crop management conditions was carried out. The characterization of phosphate rocks is the first and essential step in evaluating their suitability for direct application. If several PR sources are utilized, standardized methods should be used for comparison purposes to determine their agronomic potential. This paper describes the standard characterization of phosphate rock products utilized in the project, in particular the mineralogical and crystallographic analyses, physical analyses, chemical composition and solubility in conventional reagents. A total of 28 phosphate rock samples from 15 countries were collected and analyzed in specialized laboratories. The data on mineralogy, chemical composition and solubility in conventional reagents are closely interrelated. An arbitrary classification of the reactivity of the PR samples was made based on the solubility indices in conventional reagents. On another hand, the results of the crystallographic parameters, calculated indices of absolute solubility, specific surface and porosity reflect the variability of the physical state and the sample pre-conditioning treatment of the analyzed products. A proper characterization of phosphate rock samples should provide the maximum of basic information that can be obtained in a cost-effective manner in normal chemical laboratories. Based on the results of this characterization, the following determinations are recommended: a description of the sample, major elemental (total P, Ca, Mg) composition, solubility in conventional reagents (neutral ammonium citrate, citric and formic acid) and particle size analysis. The classification of PR samples for direct

  17. DETECTION OF THE AMMONIUM ION IN SPACE

    International Nuclear Information System (INIS)

    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.

    2013-01-01

    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 0 -0 0 line of the deuterated ammonium ion, NH 3 D + . 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 3 D + as the electric field over the N nucleus is practically zero. Moreover, the feature is right at the predicted frequency for the 1 0 -0 0 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) × 10 12 cm –2 . Assuming a deuterium enhancement similar to that of NH 2 D, we derive N(NH 4 + ) ≅ 2.6 × 10 13 cm –2 , i.e., an abundance for ammonium of a few 10 –11 .

  18. DETECTION OF THE AMMONIUM ION IN SPACE

    Energy Technology Data Exchange (ETDEWEB)

    Cernicharo, J.; Tercero, B. [Deparment of Astrophysics, CAB, INTA-CSIC, Crta Torrejon-Ajalvir Km 4, E-28850 Torrejon de Ardoz, Madrid (Spain); Fuente, A. [Observatorio Astronomico Nacional, Apdo. 112, E-28803 Alcala de Henares (Spain); Domenech, J. L.; Cueto, M.; Carrasco, E.; Herrero, V. J.; Tanarro, I. [Instituto de Estructura de la Materia, IEM-CSIC, Serrano 123, E-28006 Madrid (Spain); Marcelino, N. [NRAO, 520 Edgemont Road, Charlottesville, VA 22902 (United States); Roueff, E. [Luth, Observatoire de Paris, CNRS UMR8102, Place J. Janssen F-92190 Meudon (France); Gerin, M. [LERMA, Observatoire de Paris, CNRS UMR8112 and Ecole Normale Superieure, 61 Avenue de lObservatoire, F-75014 Paris (France); Pearson, J., E-mail: jcernicharo@cab.inta-csic.es [Jet Propulsion Laboratory, 4800 Oak Grove Drive, MC 168-314, Pasadena, CA 91109 (United States)

    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}.

  19. Surface deterioration of ammonium acid phthalate crystals

    Energy Technology Data Exchange (ETDEWEB)

    Barrus, D.M.; Blake, R.L.; Burek, A.J.

    1976-01-01

    In working with various acid phthalate crystals for low energy X-ray spectroscopy, we have observed a relatively rapid surface degradation of ammonium acid phthalate in comparison with similar crystals was observed. It was found that two different samples degraded in a few days upon exposure to high vacuum (10/sup -6/ - 10/sup -7/ torr). The same crystals showed similar effects when exposed to room atmosphere for two to three weeks. One of these crystals deteriorated while kept constantly in a desiccator jar for about two years. The desiccator environment seems to be the most favorable. The observed difference in the surface of these crystals might be described as a change from a transparent, glasslike condition to a white, powderlike haze somewhat akin to frosted glass. A two week exposure to vacuum for a freshly cleaved crystal caused the integrated coefficient of reflection at 23.6 A to decrease by a factor of 2.5. The degraded surface areas tend to form definite rhombohedral patterns. Since the external symmetry of ammonium acid phthalate crystals is rhombohedral, this suggests that the degradation we observe takes place in the form of large etched figures. A possible mechanism may be sublimation, which would proceed more rapidly in vacuum than in air. It is concluded that ammonium acid phthalate should be kept in a desiccator environment as much as possible. Exposures to vacuum should be brief and critical diffraction measurements should be done using a freshly cleaved surface.

  20. Microbial electricity driven anoxic ammonium removal.

    Science.gov (United States)

    Vilajeliu-Pons, Anna; Koch, Christin; Balaguer, Maria D; Colprim, Jesús; Harnisch, Falk; Puig, Sebastià

    2018-03-01

    Removal of nitrogen, mainly in form of ammonium (NH 4 + ), in wastewater treatment plants (WWTPs) is a highly energy demanding process, mainly due to aeration. It causes costs of about half a million Euros per year in an average European WWTP. Alternative, more economical technologies for the removal of nitrogen compounds from wastewater are required. This study proves the complete anoxic conversion of ammonium (NH 4 + ) to dinitrogen gas (N 2 ) in continuously operated bioelectrochemical systems at the litre-scale. The removal rate is comparable to conventional WWTPs with 35 ± 10 g N m -3 d -1 with low accumulation of NO 2 - , NO 3 - , N 2 O. In contrast to classical aerobic nitrification, the energy consumption is considerable lower (1.16 ± 0.21 kWh kg -1 N, being more than 35 times less than for the conventional wastewater treatment). Biotic and abiotic control experiments confirmed that the anoxic nitrification was an electrochemical biological process mainly performed by Nitrosomonas with hydroxylamine as the main substrate (mid-point potential, E ox  = +0.67 ± 0.08 V vs. SHE). This article proves the technical feasibility and reduction of costs for ammonium removal from wastewater, investigates the underlying mechanisms and discusses future engineering needs. Copyright © 2017 Elsevier Ltd. All rights reserved.

  1. Mechanism of the Topotactic Formation of gamma-Zirconium Phosphate Covalently Pillared with Diphosphonate Groups.

    Science.gov (United States)

    Alberti, G.; Giontella, E.; Murcia-Mascarós, S.; Vivani, R.

    1998-09-07

    The topotactic reaction of gamma-ZrPO(4)[O(2)P(OH)(2)].2H(2)O (gamma-ZrP) with benzenediphosphonic acid was examined in water and in acetone-water mixtures. This reaction was found to take place in water only on the external surface of the microcrystals, and pillared compounds were never obtained, even after very long reaction times. On the contrary, covalently pillared compounds were quickly obtained in acetone-water mixtures. The mechanism of the latter topotactic reaction was investigated by determining the rate of the phosphate groups released and the rate of the benzenediphosphonates taken up by gamma-ZrP over a long time (50 days). These data showed that pillared derivatives of gamma-ZrP can be obtained because colloidal dispersions of exfoliated lamellae are formed in acetone-water mixtures. The diphosphonate group acts initially as a monovalent species, replacing only one dihydrogen phosphate group on the surface of the exfoliated gamma-lamellae. The colloidal and partially derivatized lamellae thus formed can interact with each other by forming polylamellar pillared systems. When the number of pillared lamellae exceeds a given value (usually 5-6), flocculation of the colloidal gamma-ZrP takes place. Topotactic reactions between packets of pillared lamellae may also continue in the flocculated system. Therefore, the average number of the pillared lamellae slowly increases over time.

  2. Effects of phosphate addition on methane fermentation in the batch and upflow anaerobic sludge blanket (UASB) reactors.

    Science.gov (United States)

    Suzuki, Sho; Shintani, Masaki; Sanchez, Zoe Kuizon; Kimura, Kohei; Numata, Mitsuru; Yamazoe, Atsushi; Kimbara, Kazuhide

    2015-12-01

    Ammonia inhibition of methane fermentation is one of the leading causes of failure of anaerobic digestion reactors. In a batch anaerobic digestion reactor with 429 mM NH3-N/L of ammonia, the addition of 25 mM phosphate resulted in an increase in methane production rate. Similar results were obtained with the addition of disodium phosphate in continuous anaerobic digestion using an upflow anaerobic sludge blanket (UASB) reactor. While methane content and production rate decreased in the presence of more than 143 mM NH3-N/L of ammonium chloride in UASB, the addition of 5 mM disodium phosphate suppressed ammonia inhibition at 214 mM NH3-N/L of ammonium chloride. The addition prevented acetate/propionate accumulation, which might be one of the effects of the phosphate on the ammonia inhibition. The effects on the microbial community in the UASB reactor was also assessed, which was composed of Bacteria involved in hydrolysis, acidogenesis, acetogenesis, and dehydrogenation, as well as Archaea carrying out methanogenesis. The change in the microbial community was observed by ammonia inhibition and the addition of phosphate. The change indicates that the suppression of ammonia inhibition by disodium phosphate addition could stimulate the activity of methanogens, reduce shift in bacterial community, and enhance hydrogen-producing bacteria. The addition of phosphate will be an important treatment for future studies of methane fermentation.

  3. Phosphates nanoparticles doped with zinc and manganese for sunscreens

    Energy Technology Data Exchange (ETDEWEB)

    Araujo, T.S. de, E-mail: tatiana.araujo@ifs.edu.br [Departamento de Fisica, Universidade Federal de Sergipe, Sergipe (Brazil); Instituto Federal de Ciencias e Tecnologia de Sergipe, Sergipe (Brazil); Souza, S.O. de [Departamento de Fisica, Universidade Federal de Sergipe, Sergipe (Brazil); Miyakawa, W. [Divisao de Fotonica - Instituto de Estudos Avancados, Sao Jose dos Campos (Brazil); Sousa, E.M.B. de [Centro de Desenvolvimento de Tecnologia Nuclear - CDTN/CNEN, Minas Gerais (Brazil)

    2010-12-01

    The crescent number of skin cancer worldwide gives impulse to the development of sunscreen that can both prevent skin cancer and also permit gradual tanning. In this work, the synthesis of hydroxyapatite and tricalcium phosphate nanocrystalline powders was investigated in order to obtain materials with optical properties and appropriate size for sunscreen. Pure, Zn{sup 2+}-doped and Mn{sup 2+}-doped hydroxyapatite (HAP) and tricalcium phosphate ({beta}-TCP) were produced by the wet precipitation process using diammonium phosphate, calcium nitrate, ammonium hydroxide, zinc nitrate and manganese nitrate as reagents. The pure and doped HAP precipitates were calcined at 500 deg. C for 1 h, while the {beta}-TCP (pure and doped) were calcined at 800 deg. C for 2 h. The powder samples were characterized by X-ray diffraction (XRD), energy dispersive X-ray fluorescence (EDX), atomic force microscopy (AFM) and ultraviolet (UV)-vis spectroscopy. XRD and EDX showed the formation of the expected materials (HAP and {beta}-TCP) without toxic components. AFM micrographs showed aggregated ellipsoidal particles with dimensions smaller than 120 nm. Optical absorption spectra showed that the calcium phosphate produced in this work absorbs in the UV region. The obtained materials presented structural, morphological and optical properties that allow their use as the active centers in sunscreens.

  4. Phosphates nanoparticles doped with zinc and manganese for sunscreens

    International Nuclear Information System (INIS)

    Araujo, T.S. de; Souza, S.O. de; Miyakawa, W.; Sousa, E.M.B. de

    2010-01-01

    The crescent number of skin cancer worldwide gives impulse to the development of sunscreen that can both prevent skin cancer and also permit gradual tanning. In this work, the synthesis of hydroxyapatite and tricalcium phosphate nanocrystalline powders was investigated in order to obtain materials with optical properties and appropriate size for sunscreen. Pure, Zn 2+ -doped and Mn 2+ -doped hydroxyapatite (HAP) and tricalcium phosphate (β-TCP) were produced by the wet precipitation process using diammonium phosphate, calcium nitrate, ammonium hydroxide, zinc nitrate and manganese nitrate as reagents. The pure and doped HAP precipitates were calcined at 500 deg. C for 1 h, while the β-TCP (pure and doped) were calcined at 800 deg. C for 2 h. The powder samples were characterized by X-ray diffraction (XRD), energy dispersive X-ray fluorescence (EDX), atomic force microscopy (AFM) and ultraviolet (UV)-vis spectroscopy. XRD and EDX showed the formation of the expected materials (HAP and β-TCP) without toxic components. AFM micrographs showed aggregated ellipsoidal particles with dimensions smaller than 120 nm. Optical absorption spectra showed that the calcium phosphate produced in this work absorbs in the UV region. The obtained materials presented structural, morphological and optical properties that allow their use as the active centers in sunscreens.

  5. Conditions promoting and restraining agronomic effectiveness of water-insoluble phosphate sources, in particular phosphate rock (PR): I. Indices of phosphate rock use opportunity (PRUOIS) and of phosphate rock suitability for direct use (PRSIDU)

    International Nuclear Information System (INIS)

    Borlan, Z.; Gavriluta, I.; Soare, M.; Stefanescu, D.; Alexandrescu, A.

    2002-01-01

    Several issues of phosphate rock (PR) use are discussed in this paper. Maize for green fodder (Zea mays L) and ryegrass (Lolium multiflorum Lam.) were grown in 7 kg of dry soil and in small pots of 1.25 kg dry soil capacity, respectively, on several base unsaturated soils belonging to Hapludoll and Hapludalf soil groups. The amount of phosphate rock (PR) to apply was based on experimental data considering soil adsorbed acidity (Ah), humus content (H 2 ), cation exchange capacity (T), sum of exchangeable bases (SEB) and mobile (easily soluble) phosphate content (P A L) in the soil. The factors were combined in a rock phosphate use, opportunity index of the soil (PRUOIS): PRUOIS=(A h *H 2 *100)/SEB*10 0.0245*P AL Rock phosphate suitability for direct use was evaluated by means of the rate of PR-P dissolution (PRPRS) in a 0.6% ammonium heptamolybdate in 0.01M calcium chloride solution (ppm P) and by carbonate content (%CaCO 3 ) in PR. Both of these parameters combined provided a phosphate rock suitability index for direct use (PRSIDU): PRSIDU [ppmP/min]=PRPRS*(1-0.03*CaCO 3 ) Water insoluble P sources studied were PR from Kola-Russia, Morocco, Kneifiss-Siria, El Hassa-Jordan, Gafsa- Tunisia, North-Carolina (USA), and Arad-Israel. All PRs were compared with TSP applied at the same rate of P. Neither PRUOIS or PRSIDU considered separately could satisfactorily explain the variance of PR efficiency. An index obtained by multiplicative combination of PRUOIS x PRSIDU did correlate significantly with indices on the agronomic efficiency of PR. (author)

  6. A radiochemical method for carbamoyl-phosphate synthetase I: application to rats fed a hyperproteic diet

    OpenAIRE

    Arriarán, Sofía; Agnelli, Silvia; Fernández López, José Antonio; Remesar Betlloch, Xavier; Alemany, Marià, 1946-

    2012-01-01

    A method for the measurement of carbamoyl-phosphate synthetase I activity in animal tissues has been developed using the livers of rats under normal and hyperproteic diets. The method is based on the incorporation of 14C-ammonium bicarbonate to carbamoyl-phosphate in the presence of ATP-Mg and N-acetyl-glutamate. The reaction is stopped by chilling, lowering the pH and adding ethanol. Excess bicarbonate is flushed out under a gentle stream of cold CO2. The only label remaining in the medium w...

  7. [A stable reagent for the-single stage determination of inorganic phosphate].

    Science.gov (United States)

    Pupyshev, A B

    1991-01-01

    A recipe of a simple reagent for phosphorus detection has been developed, consisting of ammonium molybdate (4 mM), sulfuric acid (0.2 N), and Tween-80 (0.2%). The developing phosphate staining may be registered in 15 min at a wavelength of 350 nm. The product molar extinction is equal to 1.20.10(4) M-1.cm-1, this being close to that of molybdic blue. Phosphate staining is characterized by the stability of results and insensitivity to the presence of a number of substances used in enzymology. The prepared reagent is fit for experiments within a fortnight if stored in the cold.

  8. Low temperature fabrication of magnesium phosphate cement scaffolds by 3D powder printing.

    Science.gov (United States)

    Klammert, Uwe; Vorndran, Elke; Reuther, Tobias; Müller, Frank A; Zorn, Katharina; Gbureck, Uwe

    2010-11-01

    Synthetic bone replacement materials are of great interest because they offer certain advantages compared with organic bone grafts. Biodegradability and preoperative manufacturing of patient specific implants are further desirable features in various clinical situations. Both can be realised by 3D powder printing. In this study, we introduce powder-printed magnesium ammonium phosphate (struvite) structures, accompanied by a neutral setting reaction by printing farringtonite (Mg(3)(PO(4))(2)) powder with ammonium phosphate solution as binder. Suitable powders were obtained after sintering at 1100°C for 5 h following 20-40 min dry grinding in a ball mill. Depending on the post-treatment of the samples, compressive strengths were found to be in the range 2-7 MPa. Cytocompatibility was demonstrated in vitro using the human osteoblastic cell line MG63.

  9. Z-H Bond Activation in (Di)hydrogen Bonding as a Way to Proton/Hydride Transfer and H2 Evolution.

    Science.gov (United States)

    Belkova, Natalia V; Filippov, Oleg A; Shubina, Elena S

    2018-02-01

    The ability of neutral transition-metal hydrides to serve as a source of hydride ion H - or proton H + is well appreciated. The hydride ligands possessing a partly negative charge are proton accepting sites, forming a dihydrogen bond, M-H δ- ⋅⋅⋅ δ+ HX (M=transition metal or metalloid). On the other hand, some metal hydrides are able to serve as a proton source and give hydrogen bond of M-H δ+ ⋅⋅⋅X type (X=organic base). In this paper we analyse recent works on transition-metal and boron hydrides showing i) how formation of an intermolecular complex between the reactants changes the Z-H (M-H and X-H) bond polarity and ii) what is the implication of such activation in the mechanisms of hydrides reactions. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Renal phosphate handling: Physiology

    Directory of Open Access Journals (Sweden)

    Narayan Prasad

    2013-01-01

    Full Text Available Phosphorus is a common anion. It plays an important role in energy generation. Renal phosphate handling is regulated by three organs parathyroid, kidney and bone through feedback loops. These counter regulatory loops also regulate intestinal absorption and thus maintain serum phosphorus concentration in physiologic range. The parathyroid hormone, vitamin D, Fibrogenic growth factor 23 (FGF23 and klotho coreceptor are the key regulators of phosphorus balance in body.

  11. Quartz crystal microbalance sensor using ionophore for ammonium ion detection.

    Science.gov (United States)

    Kosaki, Yasuhiro; Takano, Kosuke; Citterio, Daniel; Suzuki, Koji; Shiratori, Seimei

    2012-01-01

    Ionophore-based quartz crystal microbalance (QCM) ammonium ion sensors with a detection limit for ammonium ion concentrations as low as 2.2 microM were fabricated. Ionophores are molecules, which selectively bind a particular ion. In this study, one of the known ionophores for ammonium, nonactin, was used to detect ammonium ions for environmental in-situ monitoring of aquarium water for the first time. To fabricate the sensing films, poly(vinyl chloride) was used as the matrix for the immobilization of nonactin. Furthermore, the anionic additive, tetrakis (4-chlorophenyl) borate potassium salt and the plasticizer dioctyl sebacate were used to enhance the sensor properties. The sensor allowed detecting ammonium ions not only in static solution, but also in flowing water. The sensor showed a nearly linear response with the increase of the ammonium ion concentration. The QCM resonance frequency increased with the increase of ammonium ion concentration, suggesting a decreasing weight of the sensing film. The detailed response mechanism could not be verified yet. However, from the results obtained when using a different plasticizer, nitrophenyl octyl ether, it is considered that this effect is caused by the release of water molecules. Consequently, the newly fabricated sensor detects ammonium ions by discharge of water. It shows high selectivity over potassium and sodium ions. We conclude that the newly fabricated sensor can be applied for detecting ammonium ions in aquarium water, since it allows measuring low ammonium ion concentrations. This sensor will be usable for water quality monitoring and controlling.

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

    International Nuclear Information System (INIS)

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

    2012-01-01

    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. - Highlights: ► Headwaters draining eroded South Pennine (UK) peatlands are nitrogen saturated. ► Ammonium and nitrate leaching arises from aeration due to lower water tables. ► Nitrate deposition equals export during storms; ammonium export exceeds input. ► Ammonia input from high atmospheric loading and mineralisation of organic nitrogen. ► Downstream nitrogen trends indicate rapid transformation of ammonium into nitrate. - Inorganic nitrogen leaching from South Pennine peatlands is dominated by ammonium that is rapidly transformed within-streams to nitrate.

  13. Ammonium vanadate titrimetric method for determination of micro amount uranium in rock and soil by using vanadate-gold indicator

    International Nuclear Information System (INIS)

    Li Yucheng.

    1990-01-01

    A new vanadate-gold indicator was successfully applied to the ammonium vanadate titrimetric method for determination of micro amount uranium in rock and soil. Uranium in 0.1g of sample is reduced by titanium trichloride in phosphoric acid. Excessive Ti (III) and other low-valent ions are oxidized by sodium nitrite, while the complex of uranium (IV)-phosphate is not oxidized. Excessive nitrite is destroyed by urea. When the concentration of phosphoric acid is 22-24 % , adding two drops of vanadate-gold indicator, uranium (IV) is titrated by standardized ammonium vanadate solution (T = 0.02-20gU/ml) and the end-point is judged by a violet-red color appearance

  14. Triphenyl phosphate allergy from spectacle frames

    DEFF Research Database (Denmark)

    Carlsen, L; Andersen, K E; Egsgaard, Helge

    1986-01-01

    A case of triphenyl phosphate allergy from spectacle frames is reported. Patch tests with analytical grade triphenyl phosphate, tri-m-cresyl phosphate, and tri-p-cresyl phosphate in the concentrations 5%, 0.5% and 0.05% pet. showed positive reactions to 0.05% triphenyl phosphate and 0.5% tri......-m-cresyl phosphate, but no reaction to tri-p-cresyl phosphate. Gas chromatography of the tricresyl phosphate 5% pet. patch test material supplied from Trolab showed that it contained a mixture of a wide range of triaryl phosphates, including 0.08% triphenyl phosphate which is above the threshold for detecting...

  15. Modificated ammonium nitrate based on its melt and bentonic clay

    OpenAIRE

    TURDIALIEV UMID MUHTARALIEVICH; NAMAZOV SHAFOAT SATTAROVICH; REYMOV AHMED MAMBETKARIMOVICH; BEGLOV BORIS MIHAYLOVICH; MIRSALIMOVA SAODAT RAHMATJANOVNA

    2016-01-01

    The approaches of nonexplosive ammonium nitrate by mean introduction of different inorganic matter into ammonium nitrate’s composition have been analyzed in the study. The results of thermostable ammonium nitrate obtain using Azkamarsk, Lagonsk, Kattakurgansk, and Navbahorsk bentonite from Uzbekistan as an additive, have been given. Composition and property (granule strength, modification transition temperature, thermal effect of modification transition, dimensions of granule’s micropores and...

  16. Microbial Leaching of Some Valuable Elements From Egyptian Phosphate Rock

    International Nuclear Information System (INIS)

    Kamal, H.M.; Hassanein, R.A.; Mahdy, H.M.A.; Mahmoud, K.F.; Abouzeid, M.A.

    2012-01-01

    Four phosphate rock samples representing different phosphate mineralization modes in Egypt were selected from Abu Tartar, Nile valley and Red sea areas. Factors affecting the phosphate rock solubilization and some of the contained valuable elements by Aspergillus niger, Penicillium sp. and Pseudomonas fluorescence, were studied with especial orientation towards the completion of phosphate rock samples solubilization especially die low grade one. Effect of nitrogen source type on leaching efficiency by Aspergillus niger when two nitrogen sources on the phosphate bioleaching efficiency, it is clear that the ammonium chloride is more favorable as nitrogen source than sodium nitrate in the bioleaching of phosphate rocks. When Aspergillus niger was applied under die following conditions: 50 g/1 of sucrose as a carbon source, 0.1 N of ammonium chloride as a nitrogen source, 10 days incubation period, 0.5% solid: liquid ratio for P 2 O 5 and 5% for U and REE and - 270 mesh of grain size. The optimum leaching of P 2 O 5 , U and REE from phosphate rock samples reached (23.27%, 17.4%, 11.4%, respectively), while at -60 mesh they reached to 16.58%, 28.9%, 30.2% respectively. The optimum conditions for the maximal leaching efficiencies of P 2 O 5 , U and REE when applying the Penicillium sp. from the phosphate rock samples were: 100 g/1 of sucrose as a carbon source for P 2 O 5 and U and 10 g/1 for REE, 7,15 and 10 days incubation period for P 2 O 5 , U and REE, respectively, 0.5% solid: liquid ratio for P 2 O 5 and 5% for U and REE. Finally, the application of phosphate rock samples grinded to -270 mesh of grain size for P 2 O 5 and (-60 to -140) for U and REE. The studied leaching efficiency of P 2 O 5 , U and REE gave at -270 mesh 33.66%, 24.3%, 15.9% respectively, while at -60 mesh they gave 33.76%, 26.7%, 17.8% and at -140 mesh gave 31.32%, 27.9%, 17.6%, respectively.The optimum conditions for the P 2 O 5 leaching efficiency when applying the Pseudomonas fluorescence were

  17. Safety Testing of Ammonium Nitrate Based Mixtures

    Science.gov (United States)

    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.

  18. Quaternary Ammonium Polyethyleneimine: Antibacterial Activity Ira

    International Nuclear Information System (INIS)

    Farber, Y.; Domb, A.G.; Golenser, J.; Beyth, N.; Weiss, E.I.

    2010-01-01

    Quaternary ammonium polyethyleneimine- (QA-PEI-) based nanoparticles were synthesized using two synthetic methods, reductive amination and N-alkylation. According to the first method, QA-PEI nanoparticles were synthesized by cross-linking with glutaraldehyde followed by reductive amination with octanal and further N-methylation with methyl iodide. The second method is based on crosslinking with dialkyl halide followed by N-alkylation with octyl halide and further N-methylation with methyl iodide. QA-PEI nanoparticles completely inhibited bacterial growth (>106 bacteria), including both Gram-positive, that is, Staphylococcus aureus at 80 μ/mL, and Gram-negative, that is, Escherichia coli at 320 μ/mL. Activity analysis revealed that the degree of alkylation and N-methylation of the QA-PEI nanoparticles plays a significant role in antibacterial activity of the reagent. The most potent compound was octyl alkylated QA-PEI alkylated at 1 : 1 mole ratio (primary amine of PEI monomer units/alkylating agent). Also, cytotoxicity studies on MAT-LyLu and MBT cell lines were performed with QA-PEI nanoparticles. These findings confirm previous reports that poly cations bearing quaternary ammonium moieties inhibit bacterial growth in vitro and have a potential use as additives in medical devices which need antibacterial properties.

  19. Integrated assessment of the phosphate industry

    International Nuclear Information System (INIS)

    Ryan, M.T.; Cotter, S.J.

    1980-05-01

    The phosphate industry in the United States includes three major activities, namely, mining and milling of phosphate rock, phosphate product manufacture, and phosphate product use. Phosphatic materials contain uranium, thorium, and their decay products in greater than background amounts. This assessment of the radiological impacts associated with the redistribution of radioactive components of phosphate materials may provide insight into the effects of uranium extraction from phosphate materials for use in the nuclear fuel cycle

  20. Changes in soil toxicity by phosphate-aided soil washing: effect of soil characteristics, chemical forms of arsenic, and cations in washing solutions.

    Science.gov (United States)

    Jho, Eun Hea; Im, Jinwoo; Yang, Kyung; Kim, Young-Jin; Nam, Kyoungphile

    2015-01-01

    This study was set to investigate the changes in the toxicity of arsenic (As)-contaminated soils after washing with phosphate solutions. The soil samples collected from two locations (A: rice paddy and B: forest land) of a former smelter site were contaminated with a similar level of As. Soil washing (0.5 M phosphate solution for 2 h) removed 24.5% As, on average, in soil from both locations. Regardless of soil washing, Location A soil toxicities, determined using Microtox, were greater than that of Location B and this could be largely attributed to different soil particle size distribution. With soils from both locations, the changes in As chemical forms resulted in either similar or greater toxicities after washing. This emphasizes the importance of considering ecotoxicological aspects, which are likely to differ depending on soil particle size distribution and changes in As chemical forms, in addition to the total concentration based remedial goals, in producing ecotoxicologically-sound soils for reuse. In addition, calcium phosphate used as the washing solution seemed to contribute more on the toxic effects of the washed soils than potassium phosphate and ammonium phosphate. Therefore, it would be more appropriate to use potassium or ammonium phosphate than calcium phosphate for phosphate-aided soil washing of the As-contaminated soils. Copyright © 2014 Elsevier Ltd. All rights reserved.

  1. Better prospects for phosphate production

    Energy Technology Data Exchange (ETDEWEB)

    1980-06-01

    The extraction of uranium as a by product of phosphate production is discussed. Techniques being commercially developed are described. The trend towards the wet process, in which sulphuric acid is used to dissolve the phosphate, producing phosphoric acid, is also the preferred method for uranium recovery. Recovery from a wet process phosphoric acid stream, integrated with phosphate fertilizer manufacture, is becoming increasingly commercially viable for the production of yellow-cake.

  2. on association of trialkyl phosphates

    International Nuclear Information System (INIS)

    Petkovic, D.M.; Maksimovic, Z.B.

    1976-01-01

    The association constants of tri-n-butyl (TBP), tri-n-propyl (TPP) and triethyl phosphate (TEP) with chloroform, carbon tetrachloride and benzene were determined by dielectric constant, proton magnetic resonance and vapor pressure measurements. Correlation of the trialkyl phosphate-chloroform association constants, using the Hammett equation, showed their increase with the number of carbon atoms in the aliphatic radicals. The change of trialkyl phosphate reactivity with temperature was used to determine the thermodynamic quantities. (author)

  3. Flotation separation of strontium via phosphate precipitation.

    Science.gov (United States)

    Thanh, Luong H V; Liu, J C

    2017-06-01

    Flotation separation of strontium (Sr) from wastewater via phosphate precipitation was investigated. While 37.33% of Sr precipitated at highly alkaline pH in the absence of PO 4 3- , it completely precipitated as Sr 3 (PO 4 ) 2 at a molar ratio ([PO 4 3- ]:[Sr 2+ ]) of 0.62 at a lower pH value. The presence of Ca 2+ hindered Sr precipitation, yet it could be overcome by increasing the PO 4 3- dose. Sodium dodecyl sulfate (SDS) was a better collector for dispersed air flotation of Sr 3 (PO 4 ) 2 than cetyl trimethyl ammonium bromide, or mixed collector systems of SDS and saponin. The highest separation efficiency of 97.5% was achieved at an SDS dose of 40 mg/L. The main mechanism in the precipitate flotation is adsorption of anionic SDS on the positively charged surface of colloidal Sr 3 (PO 4 ) 2 via electrostatic interaction. SDS enhanced the aggregation of Sr 3 (PO 4 ) 2 precipitates as the size increased from 1.65 to 28.0 μm, which was beneficial to separation as well.

  4. Phosphate Recovery From Sewage Sludge Containing Iron Phosphate

    NARCIS (Netherlands)

    Wilfert, P.K.

    2018-01-01

    The scope of this thesis was to lay the basis for a phosphate recovery technology that can be applied on sewage sludge containing iron phosphate. Such a technology should come with minimal changes to the existing sludge treatment configuration while keeping the use of chemicals or energy as small as

  5. 21 CFR 137.175 - Phosphated flour.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 2 2010-04-01 2010-04-01 false Phosphated flour. 137.175 Section 137.175 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN... Related Products § 137.175 Phosphated flour. Phosphated flour, phosphated white flour, and phosphated...

  6. Removal of phosphate from greenhouse wastewater using hydrated lime.

    Science.gov (United States)

    Dunets, C Siobhan; Zheng, Youbin

    2014-01-01

    Phosphate (P) contamination in nutrient-laden wastewater is currently a major topic of discussion in the North American greenhouse industry. Precipitation of P as calcium phosphate minerals using hydrated lime could provide a simple, inexpensive method for retrieval. A combination of batch experiments and chemical equilibrium modelling was used to confirm the viability of this P removal method and determine lime addition rates and pH requirements for greenhouse wastewater of varying nutrient compositions. Lime: P ratio (molar ratio of CaMg(OH)₄: PO₄‒P) provided a consistent parameter for estimating lime addition requirements regardless of initial P concentration, with a ratio of 1.5 providing around 99% removal of dissolved P. Optimal P removal occurred when lime addition increased the pH from 8.6 to 9.0, suggesting that pH monitoring during the P removal process could provide a simple method for ensuring consistent adherence to P removal standards. A Visual MINTEQ model, validated using experimental data, provided a means of predicting lime addition and pH requirements as influenced by changes in other parameters of the lime-wastewater system (e.g. calcium concentration, temperature, and initial wastewater pH). Hydrated lime addition did not contribute to the removal of macronutrient elements such as nitrate and ammonium, but did decrease the concentration of some micronutrients. This study provides basic guidance for greenhouse operators to use hydrated lime for phosphate removal from greenhouse wastewater.

  7. Preparation and thermogravimetric study of some uranyl phosphates

    International Nuclear Information System (INIS)

    Schaekers, J.M.

    1970-10-01

    The preparation of uranyl ammonium phosphate trihydrate (UAP = UO 2 NH 4 PO 4 .3H 2 O), acid uranyl phosphate tetrahydrate(AUP = UO 2 HPO 4 .4H 2 O) and neutral uranyl phosphate tetrahydrate (NUPT = (UO 2 ) 3 (PO 4 ) 2 .4H 2 O) was investigated during the data from the literature. The thermal decomposition in different atmospheres, such as air, oxygen, nitrogen and argon, was studied in the temperature range 25-1000 0 C. It was found that the pyrophosphate U 2 O 3 P 2 O 7 is a stable decomposition product of UAP as well as of AUP. A mixture of U 3 O 8 and U 2 O 3 P 2 O 7 is obtained when the NUPT is decomposed in an oxygen-free atmosphere. NUPT however is stable in an oxidising atmosphere. Hydrogen and carbon reductions were also carried out, and UO 2 or (UO) 2 P 2 O 7 as well as mixtures of these two products can be obtained, depending on the starting material and the reduction temperature. The different reduction and decomposition reactions were studied by means of thermogravimetric analysis, and activation energies were calculated where possible. I.R. spectral analysis was also used to identify various products with the same composition [af

  8. FRACTIONATION AND CHARACTERISATION OF TECHNICAL AMMONIUM LIGNOSULPHONATE

    Directory of Open Access Journals (Sweden)

    Cheryl Ann Leger

    2010-08-01

    Full Text Available It is difficult to use lignin in any analytical methodology without reducing its considerable polydispersity by fractionation. An ammonium lignosulphonate sample was fractionated using a method of partial solubility in solutions of isopropanol increasingly diluted with distilled water, effectively fractionating by polarity. Selected fractions were characterised by gravimetric determination of the fractions, and determination of acid insoluble lignin, soluble lignin, and carbohydrate contents. Acid-insoluble lignin content was very low, and soluble lignin provided the majority of the lignin content, as should be expected from sulphonated lignin. Carbohydrate contents were also fairly low, the highest percentage at 14.5 being in Fraction 2, with the bulk lignin and Fraction 3 having 6.5% and 3.2%, respectively. Differences in the composition of each fraction support the efficacy of the fractionation process and permitted selection of fractions for use in subsequent studies.

  9. Double selenates of rare earths and ammonium

    International Nuclear Information System (INIS)

    Iskhakova, L.D.; Kozlova, N.P.; Makarevich, L.G.

    1991-01-01

    Double selenates of rare earths with ammonium were prepared in result of crystallization. It is shown that NH 4 Ln(SeO 4 ) · nH 2 O crystalline hydrates are presented by penta-and trihydrates. Existance of two modifications was revealed for NH 4 Ln(SeO 4 ) · 5H 2 O: monoclinic form of NH 4 La(SeO 4 ) 2 · 5H 2 O, isostructural RbCe(SeO 4 ) 2 · 5H 2 O, and earlier unknown rhombic form of salts with Ln = Pr, Nd. Trihydrates with Ln = Sm-Yb belong to structural type of RbNd(SeO 4 ) 2 · 3H 2 O. Anhydrous salts NH 4 Ln(SeO 4 ) 2 are isostructural with monoclinic KNd(SO 4 ) 2 modification. Lattice parameters of binary selenates are presented

  10. Hydration Structure of the Quaternary Ammonium Cations

    KAUST Repository

    Babiaczyk, Wojtek Iwo

    2010-11-25

    Two indicators of the hydropathicity of small solutes are introduced and tested by molecular dynamics simulations. These indicators are defined as probabilities of the orientation of water molecules\\' dipoles and hydrogen bond vectors, conditional on a generalized distance from the solute suitable for arbitrarily shaped molecules. Using conditional probabilities, it is possible to distinguish features of the distributions in close proximity of the solute. These regions contain the most significant information on the hydration structure but cannot be adequately represented by using, as is usually done, joint distance-angle probability densities. Our calculations show that using our indicators a relative hydropathicity scale for the interesting test set of the quaternary ammonium cations can be roughly determined. © 2010 American Chemical Society.

  11. Ammonium and methylammonium transport in Rhodobacter sphaeroides

    International Nuclear Information System (INIS)

    Cordts, M.L.; Gibson, J.

    1987-01-01

    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 4 + to washed, nitrogen-free cell suspensions was followed by linear uptake of NH 4 + from the medium and transient formation of intracellular pools of 0.9 to 1.5 mM NH 4 + . Transport of NH 4 + was shown to be independent of assimilation by glutamine synthetase because intracellular pools of over 1 mM represented NH 4 + 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 4 + -free cell suspensions, methylammonium ( 14 CH 3 NH 3 + ) was taken up rapidly, and intracellular concentrations of 0.4 to 0.5 mM were maintained. The 14 CN 3 NH 3 + pool was not affected by methionine sulfoximine. Unlike NH 4 + uptake, 14 CH 3 NH 3 + uptake in nitrogen-free cell suspensions was repressed by growth in NH 4 + . These results suggest that R. sphaeroides may produce an NH 4 + -specific transport system in addition to the NH 4 + / 14 CH 3 NH 3 + transporter. This second transporter is able to produce normal-size NH 4 + pools but has very little affinity for 14 CH 3 NH 3 + and is not repressed by growth in high concentrations of NH 4 +

  12. Ammonium and hydroxylamine uptake and accumulation in Nitrosomonas

    NARCIS (Netherlands)

    Schmidt, I.; Look, C.; Bock, E.; Jetten, M.S.M.

    2004-01-01

    Starved cells of Nitrosomonas europaea and further ammonia oxidizers were able to rapidly accumulate ammonium and hydroxylamine to an internal concentration of about 1 and 0.8 M, respectively. In kinetic studies, the uptake/accumulation rates for ammonium [3.1 mmol (g protein)(-1) min(-1)] and

  13. 78 FR 32690 - Certain Ammonium Nitrate From Ukraine

    Science.gov (United States)

    2013-05-31

    ... From Ukraine Determination On the basis of the record \\1\\ developed in the subject five-year review... certain ammonium nitrate from Ukraine would be likely to lead to continuation or recurrence of material... Ammonium Nitrate from Ukraine: Investigation No. 731-TA-894 (Second Review). By order of the Commission...

  14. Ginger-supplemented diet ameliorates ammonium nitrate-induced ...

    African Journals Online (AJOL)

    The present study was designed to evaluate the capacity of ginger to repair the oxidative stress induced by ammonium nitrate. 50 male rats were divided into 5 groups; they underwent an oral treatment of ammonium nitrate and/or ginger (N mg/kg body weight + G% in diet) during 30 days. Group I served as control (C); ...

  15. Ammonium nitrate-polymer glasses: a new concept for phase and thermal stabilization of ammonium nitrate.

    Science.gov (United States)

    Lang, Anthony J; Vyazovkin, Sergey

    2008-09-11

    Dissolving of ammonium nitrate in highly polar polymers such as poly(vinylpyrrolidone) and/or poly(acrylamide) can result in the formation of single-phase glassy solid materials, in which NH 4 (+) and NO 3 (-) are separated through an ion-dipole interaction with the polymer matrix. Below the glass transition temperature of the polymer matrix the resulting materials remain phase and thermally stable as demonstrated through the absence of decomposition as well as the solid-solid transitions and melting of ammonium nitrate. The structure of the materials is explored by Fourier transform infrared spectroscopy and density functional calculations. Differential scanning calorimetry, thermogravimetry, and isoconversional kinetic analysis are applied to characterize the thermal behavior of the materials.

  16. Uranium extraction from ores with salicylic acid; I - uranium extraction from input phosphate ore of Abu Zaabal phosphate plant, Egypt

    International Nuclear Information System (INIS)

    Hussein, E.M.

    1997-01-01

    Salicylic acid has been tested (for environmental importance) to extract U from input phosphate ore of Abu-Zaabal phosphate plant, Egypt prior to its processing for production of phosphatic fertilizers. Uranyl ion forms with this acid three stable complexes; namely [UO 2 Sal] degree, [U O 2 SaL 2 ] 2- and UO 2 SaL-3] 4- depending on the total uranyl and salicylic acid concentrations and their ratios. Study of relevant extraction factors revealed however that, the extraction process is controlled by the amount of salicylic acid used, alcohol/aqueous ratio, solid/liquid ratio and time of agitation. The obtained results showed that uranium is selectively leached by the application of such a leaching reagent. In order to recover U from the obtained pregnant leach liquor, the latter is adjusted by ammonia to PH 5-6.5, where the crystalline pp t of N H 4 [UO 2 SaL 3 ] 4 H 2 O has formed. This precipitation has been carried out after concentrating the obtained pregnant leach liquor by its recycle for U extraction from new ore batches. The precipitated ammonium uranyl tri salicylate is calcined at 500 degree C for obtaining pure orange yellow trioxide (UO 3 ) powder. On the basis of one ton ore treatment, an economic flowsheet for U recover y from the study ore material has been suggested

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

    Science.gov (United States)

    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.

  18. Electrolytic treatment of liquid waste containing ammonium nitrate

    International Nuclear Information System (INIS)

    Komori, R.; Ogawa, N.; Ohtsuka, K.; Ohuchi, J.

    1981-01-01

    A study was made on the safe decomposition of ammonium nitrate, which is the main component of α-liquid waste from plutonium fuel facilities, by means of electrolytic reduction and thermal decomposition. In the first stage, ammonium nitrate is reduced to ammonium nitrite by electrolytic reduction using an electrolyser with a cation exchange membrane as a diaphragm. In the second stage, ammonium nitrite is decomposed to N 2 and H 2 O. The alkaline region and a low temperature are preferable for electrolytic reduction and the acidic region and high temperature for thermal decomposition. A basis was established for an ammonium nitrate treatment system in aqueous solution through the operation of a bench-scale unit, and the operating data obtained was applied to the basic design of a 10-m 3 /a facility. (author)

  19. Assimilation of ammonium and nitrate nitrogen by bean plants

    International Nuclear Information System (INIS)

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

    1989-01-01

    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 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

  20. Ammonium removal using algae-bacteria consortia: the effect of ammonium concentration, algae biomass, and light.

    Science.gov (United States)

    Jia, Huijun; Yuan, Qiuyan

    2018-04-01

    In this study, the effects of ammonium nitrogen concentration, algae biomass concentration, and light conditions (wavelength and intensity) on the ammonium removal efficiency of algae-bacteria consortia from wastewater were investigated. The results indicated that ammonium concentration and light intensity had a significant impact on nitrification. It was found that the highest ammonia concentration (430 mg N/L) in the influent resulted in the highest ammonia removal rate of 108 ± 3.6 mg N/L/days, which was two times higher than the influent with low ammonia concentration (40 mg N/L). At the lowest light intensity of 1000 Lux, algae biomass concentration, light wavelength, and light cycle did not show a significant effect on the performance of algal-bacterial consortium. Furthermore, the ammonia removal rate was approximately 83 ± 1.0 mg N/L/days, which was up to 40% faster than at the light intensity of 2500 Lux. It was concluded that the algae-bacteria consortia can effectively remove nitrogen from wastewater and the removal performance can be stabilized and enhanced using the low light intensity of 1000 Lux that is also a cost-effective strategy.

  1. Kinetics Modeling and Isotherms for Adsorption of Phosphate from Aqueous Solution by Modified Clinoptilolit

    Directory of Open Access Journals (Sweden)

    Mohammad Malakootian

    2012-01-01

    Full Text Available The Phosphorous discharge into the surface water led to excessive growth of algae and eutrophication in lakes and rivers. Therefore the phosphorus removal is important due to negative effect on water resources. The aim of this study was to investigat the modification of clinoptilolite and application of modified clinoptilolite for phosphorous adsorption from aqueous solution and isotherms and kinetics modeling. Hexadecyl Trimethyl Ammonium bromide (HDTMA-Br, Hexadecyl trimethyl Ammonium Chloride (HDTMA-Cl, Sodium Decyl Sulphate (SDS and Cetrimide-C were used for modification of clinoptilolite. Experiments were conducted using jar apparatus and batch system. The effect of pH, adsorbent doses, contact time, phosphate initial concentration and particle size were studied surveyed on phosphate adsorption by modified clinoptilolite. The most common isotherms and the kinetics adsorption equations were used for determination of adsorption rate and dynamic reaction. The results showed that maximum phosphate adsorption was obtained in the pH of 7 and contact time 90min. Also it was found with the increasing of phosphate initial concentration, phosphate removal efficiency decreased significantly. Langmuir No 2 showed a good correlation compared to other isotherms (R2=0.997. Maximum adsorption capacity was obtained in 20g/L adsorbent dose (22.73mg/g. Also Interaparticle diffusion kinetics well fits with experimental data (R2=0.999 with constant rate of 3.84mg/g min0.5. The result showed that modified clinoptilolite can be used successfully as low cost and effective absorbent for phosphate removal.

  2. Ion-selective solid-phase electrode sensitive to ammonium ions

    International Nuclear Information System (INIS)

    Vlasov, Yu.G.; Milonova, M.S.; Antonov, P.P.; Bychkov, E.A.; Ehfa, A.Ya.

    1983-01-01

    Ammonium phosphomolybdate is investigated for the purpose of using it as membrane material of ammonium-selective solid-phase electrodes. Estimation of proton mobility and ion conductivity of ammonium phosphomolybdate is performed

  3. Electrochemical Reduction of Zinc Phosphate

    International Nuclear Information System (INIS)

    Kim, Chang Hwan; Lee, Jung Hyun; Shin, Woon Sup

    2010-01-01

    We demonstrated first that the electrochemical reduction of zinc phosphate in neutral phosphate buffer is possible and potentially applicable to bio-compatible rechargeable battery. The actual redox component is Zn(s)/Zn phosphate(s) and the future research about the control of crystal formation for the better cyclability is required. In lead-acid battery, the electrochemical redox reaction of Pb (s) /PbSO 4(s) is used by reducing Pb(II) and oxidizing Pb(0) in sulfate rich solution. Since both reduced form and oxidized form are insoluble, they cannot diffuse to the opposite electrodes and react. It is a very common strategy to make a stable battery electrode that a metal element is reduced and oxidized in solution containing an abundance of anion readily precipitating with the metal ion. For the application of this strategy to construction of rechargeable battery using bio-compatible electrode materials and electrolytes, the use of phosphate ion can be considered as anion readily precipitating with metal ions. If phosphate buffer with neutral pH is used as electrolyte, the better bio-compatibility will be achieved than most of rechargeable battery using strong acid, strong base or organic solvent as electrolyte solution. There are many metal ions readily precipitating with phos-phate ion, and zinc is one of them

  4. Ammonium and methylammonium transport in Rhodobacter sphaeroides

    Energy Technology Data Exchange (ETDEWEB)

    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 +/.

  5. Reaction between CO2 and phosphate to form carboxyphosphate?

    International Nuclear Information System (INIS)

    Knight, W.B.; Attwood, P.V.; Cleland, W.W.

    1986-01-01

    Carboxyphosphate (I) is thought to be an intermediate in the enzymic carboxylation of biotin by bicarbonate and MgATP, and a plausible mechanism of carboxyl transfer to the enolate of biotin involves decarboxylation to CO 2 and phosphate. Such a process would have to be reversible, however, as carboxylase reactions are reversible. To test this possibility, the authors undertook the synthesis of I under anhydrous conditions with a high mole fraction of CO 2 present. CO 2 was distilled into capillary tubes under vacuum containing dry tris-(tetrabutyl-ammonium)-phosphate in dimethylformamide. The tubes were sealed and warmed to -10 or 20 0 C and examined by 31 P NMR. Two resonances (1.7 ppm and -5.0 ppm) in addition to phosphate (3.3 ppm) were observed. The relative ratio of each peak to the phosphate one was dependent on the temperature and the concentrations of PO 4 3- and CO 2 . Upon freezing the tubes, cracking them, and release of the CO 2 , the two additional species decomposed slowly to PO 4 3- , and more rapidly to HPO 4 3- upon the addition of H 2 O. Under some conditions they observed an additional resonance (-7.0 ppm) which is most likely pyrophosphate (PP/sub i/). At high concentrations of PO 4 3- and CO 2 , PP/sub i/ was produced and precipitated from solution. The production of PP/sub i/ is most easily explained by attack of PO 4 3- on I. They are currently trying to identify the unknown species observed in the 31 P NMR spectra

  6. Subcellular localization of ammonium transporters in Dictyostelium discoideum

    Directory of Open Access Journals (Sweden)

    Davis Carter T

    2008-12-01

    Full Text Available Abstract Background With the exception of vertebrates, most organisms have plasma membrane associated ammonium transporters which primarily serve to import a source of nitrogen for nutritional purposes. Dictyostelium discoideum has three ammonium transporters, Amts A, B and C. Our present work used fluorescent fusion proteins to determine the cellular localization of the Amts and tested the hypothesis that the transporters mediate removal of ammonia generated endogenously from the elevated protein catabolism common to many protists. Results Using RFP and YFP fusion constructs driven by the actin 15 promoter, we found that the three ammonium transporters were localized on the plasma membrane and on the membranes of subcellular organelles. AmtA and AmtB were localized on the membranes of endolysosomes and phagosomes, with AmtB further localized on the membranes of contractile vacuoles. AmtC also was localized on subcellular organelles when it was stabilized by coexpression with either the AmtA or AmtB fusion transporter. The three ammonium transporters exported ammonia linearly with regard to time during the first 18 hours of the developmental program as revealed by reduced export in the null strains. The fluorescently tagged transporters rescued export when expressed in the null strains, and thus they were functional transporters. Conclusion Unlike ammonium transporters in most organisms, which import NH3/NH4+ as a nitrogen source, those of Dictyostelium export ammonia/ammonium as a waste product from extensive catabolism of exogenously derived and endogenous proteins. Localization on proteolytic organelles and on the neutral contractile vacuole suggests that Dictyostelium ammonium transporters may have unique subcellular functions and play a role in the maintenance of intracellular ammonium distribution. A lack of correlation between the null strain phenotypes and ammonia excretion properties of the ammonium transporters suggests that it is not

  7. Hydrogen permeation resistant phosphate coatings

    International Nuclear Information System (INIS)

    McGuire, J.C.

    1979-01-01

    A method for reducing hydrogen diffusion through metal wherein the metal is coated with a phosphate-radical-containing, phosphate-glass-forming material on at least one surface thereof. The coating is then heated to at least 350 0 C to form a phosphate glass. This method is especially applicable to nuclear reactors to minimize tritium diffusion. The coating is preferably formed with a solution of phosphoric acid which may also contain compounds such as MnSO 4 , SiO 2 and Na 2 Cr 2 0 7 . (author)

  8. Hydrogen permeation resistant phosphate coatings

    International Nuclear Information System (INIS)

    McGuire, J.C.

    1979-01-01

    A method for reducing hydrogen diffusion through metal is described. The metal is coated with a phosphate-radical-containing, phosphate-glass-forming material on at least one surface. The coating is then heated to at least 350 0 C to form a phosphate glass. This method is especially applicable to nuclear reactors to minimize tritium diffusion. The coating is preferably formed with a solution of phosphoric acid which may also contain compounds such as MnSO 4 , SiO 2 and Na 2 Cr 2 O 7 . (author)

  9. 15N-ammonium test in clinical research

    International Nuclear Information System (INIS)

    Jung, K.; Metzner, C.; Teichmann, B.; Leipzig Univ.

    1989-01-01

    By use of the 15 N-ammonium test the liver function is investigated under influence of hormonal contraceptives in women and in liver diseases in children. With the described noninvasive nonradioactive isotope test the ammonia detoxification capability and the urea synthesis capacity of the liver is determined by measuring of the 15 N excretion in ammonia and urea in urine after oral administering of 15 N-ammonium chloride. The 15 N-ammonium test shows a significant influence of the hormonal contraceptives on the liver function and gives diagnostic evidence for liver diseases in children. (author)

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

    Science.gov (United States)

    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.

  11. The creation of defects in ammonium halides by excitons

    International Nuclear Information System (INIS)

    Kim, L.M.

    2002-01-01

    The ammonium halides crystals and alkali halides crystals are analogous by kind chemical bonds and crystalline lattices. The anionic sublattice is identical in this crystals. It is known the main mechanism of defect creation by irradiation is radiationless decay of excitons in alkali halides crystals. The F-, H-centers are formation in this processes. However, F, H-centres are not detected in ammonium halides. The goal of this work is investigation the creation of defects in ammonium halides by excitons. We established that excitons in ammonium chlorides and bromides are similar to excitons in alkali halides. It is known excitons are self-trapped and have identical parameters of the exciton-phonon interaction in both kind crystals. It is supposed, that processes of radiationless disintegration of excitons are identical in ammonium and alkali halides. It is necessary to understand why F-, H-centers are absent in ammonium halides. V k -centres are created by the excitation of the ammonium halides crystals in the absorption band of excitons. It was established by thermoluminescence and spectrums of absorption. The V k -centers begin to migrate at 110-120 K in ammonium chlorides and bromides. The curve of thermoluminescence have peak with maximum at this temperatures. It is known V k -centers in ammonium chlorides have the absorption band at 380 nm. We discovered this absorption band after irradiation of crystals by ultra-violet. In alkali halides F-center is anionic vacancy with electron. The wave function of electron are spread ed at the cations around anionic vacancy. We established the cation NH 4 + in ammonium halides can to capture electron. The ion NH 4 2+ is unsteady. It is disintegrated to NH 3 + and H + . We suppose that excitons in ammonium and alkali halides are disintegrated identically. When cation NH 4 + capture electron, in the anionic sublattice the configuration are created in a direction (100) The indicated configuration is unsteady in relation to a

  12. Removal of uranium from ammonium nitrate solution by nanofiltration

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Runci; Yuan, Zhongwei; Yan, Taihong; Zheng, Weifang [China Institute of Atomic Energy, Beijing (China). Dept. of Radiochemistry

    2017-07-01

    Two types of nanofiltration membranes were tested to remove uranium dissolved in ammonium nitrate solution, and the influence of operating parameters as transmembrane pressure, tangential velocity and feed temperature was investigated. Experimental results showed NF270 membrane can reject more than 96% uranium and allow most (90% min) ammonium nitrate solution passed by, and with a permeate flux of 60 L/(m{sup 2}.h). Nanofiltration seems to be a promising technology for the removal of uranium and recovery of ammonium nitrate simultaneously.

  13. New quaternary ammonium salts based decontaminants

    Directory of Open Access Journals (Sweden)

    Diana M. Popescu

    2014-06-01

    Full Text Available Decontamination after terrorist attacks or industrial accidents with biological and/or chemical agents („bio-chem“ must be fast and efficient, in order to reduce the number of victims and to eliminate the consequent damages. The decontamination of living biological agents (bacteria, viruses or nonliving ones (toxins, regulators and toxic chemicals could be accomplished by reactions of hydrolysis in various experimental conditions, in particular in alkaline medium, reactions with amines or ammonia, alcohols, phenols etc. and by their transformation into less toxic degradation products. “Bio-chem” intentional or unintentional contamination is a real risk, towards which an effective management must be available to prevent and control it. Decontamination is an essential measure to protect the personnel and the environment. Synthesis and testing of new „bio-chem“ decontaminants, based on quaternary ammonium salts, complete the arsenal of protection against chemical and biological agents. The most effective selected substances could be produced and used for decontamination in accordance with legal procedures

  14. The phase diagram of ammonium nitrate

    Science.gov (United States)

    Chellappa, Raja S.; Dattelbaum, Dana M.; Velisavljevic, Nenad; Sheffield, Stephen

    2012-08-01

    The pressure-temperature (P-T) phase diagram of ammonium nitrate (AN) [NH4NO3] has been determined using synchrotron x-ray diffraction (XRD) and Raman spectroscopy measurements. Phase boundaries were established by characterizing phase transitions to the high temperature polymorphs during multiple P-T measurements using both XRD and Raman spectroscopy measurements. At room temperature, the ambient pressure orthorhombic (Pmmn) AN-IV phase was stable up to 45 GPa and no phase transitions were observed. AN-IV phase was also observed to be stable in a large P-T phase space. The phase boundaries are steep with a small phase stability regime for high temperature phases. A P-V-T equation of state based on a high temperature Birch-Murnaghan formalism was obtained by simultaneously fitting the P-V isotherms at 298, 325, 446, and 467 K, thermal expansion data at 1 bar, and volumes from P-T ramping experiments. Anomalous thermal expansion behavior of AN was observed at high pressure with a modest negative thermal expansion in the 3-11 GPa range for temperatures up to 467 K. The role of vibrational anharmonicity in this anomalous thermal expansion behavior has been established using high P-T Raman spectroscopy.

  15. Modelling an Ammonium Transporter with SCLS

    Directory of Open Access Journals (Sweden)

    Angelo Troina

    2009-10-01

    Full Text Available The Stochastic Calculus of Looping Sequences (SCLS is a recently proposed modelling language for the representation and simulation of biological systems behaviour. It has been designed with the aim of combining the simplicity of notation of rewrite systems with the advantage of compositionality. It also allows a rather simple and accurate description of biological membranes and their interactions with the environment.In this work we apply SCLS to model a newly discovered ammonium transporter. This transporter is believed to play a fundamental role for plant mineral acquisition, which takes place in the arbuscular mycorrhiza, the most wide-spread plant-fungus symbiosis on earth. Due to its potential application in agriculture this kind of symbiosis is one of the main focuses of the BioBITs project. In our experiments the passage of NH3 / NH4+ from the fungus to the plant has been dissected in known and hypothetical mechanisms; with the model so far we have been able to simulate the behaviour of the system under different conditions. Our simulations confirmed some of the latest experimental results about the LjAMT2;2 transporter. The initial simulation results of the modelling of the symbiosis process are promising and indicate new directions for biological investigations.

  16. Precipitation of ammonium diuranate : a study

    International Nuclear Information System (INIS)

    Krishnamoorthy, T.S.; Mahadevan, N.; Sankar Das, M.

    1991-01-01

    The precipitation of ammonium diuranate (ADU) forms the first step in the production of UO 2 fuel for reactors, and hence the quality and consistency of the ADU precipitate is very important in industrial operations. An investigation, on the precipitation of ADU, was carried out under conditions similar to those in industrial production, to evaluate the effect of various variables on the consistency and the quality of ADU. The variables studied were concentration of uranium and ammonia, pH, temperature and form of ammonia (gas or solution). The properties studied were the settling rate of the precipitates, surface area of the ADUs and calcined oxides and compositional characteristics of the ADUs. Multifactorial experiments and ruggedness tests were applied to identify the parameters to which the precipitation process is most vulnerable, so that such parameters may be controlled effectively. Besides, the effect and the importance of equilibrium conditions during the precipitation process, on the quality of the final ADU, was also established. The paper presents the results of these studies. (author). 6 refs., 3 figs., 7 tabs

  17. Formation and decomposition of ammoniated ammonium ions

    International Nuclear Information System (INIS)

    Ikezoe, Yasumasa; Suzuki, Kazuya; Nakashima, Mikio; Yokoyama, Atsushi; Shiraishi, Hirotsugu; Ohno, Shin-ichi

    1998-09-01

    Structures, frequencies, and chemical reactions of ammoniated ammonium ions (NH 4 + .nNH 3 ) were investigated theoretically by ab initio molecular orbital calculations and experimentally by observing their formation and decomposition in a corona discharge-jet expansion process. The ab initio calculations were carried out using a Gaussian 94 program, which gave optimized structures, binding energies and harmonic vibrational frequencies of NH 4 + .nNH 3 . Effects of discharge current, the reactant gas and the diameter of the gas expanding pinhole were examined on the size n distribution of NH 4 + .nNH 3 . The results indicated that the cluster ion, in the jet expansion process, grew in size mostly equal to or less than one unit under experimental conditions employed. Effects of discharge current, pinhole diameter, flight time in vacuum and cluster size were examined on the decomposition rate of cluster ions formed. In our experimental conditions, the internal energies of cluster ions were mainly determined through exo- and/or endo-thermic reactions involved in the cluster formation process. (author)

  18. Calcium phosphates for biomedical applications

    Directory of Open Access Journals (Sweden)

    Maria Canillas

    2017-05-01

    Full Text Available The history of calcium phosphates in the medicine field starts in 1769 when the first evidence of its existence in the bone tissue is discovered. Since then, the interest for calcium phosphates has increased among the scientific community. Their study has been developed in parallel with new advances in materials sciences, medicine or tissue engineering areas. Bone tissue engineering is the field where calcium phosphates have had a great importance. While the first bioceramics are selected according to bioinert, biocompatibility and mechanical properties with the aim to replace bone tissue damaged, calcium phosphates open the way to the bone tissue regeneration challenge. Nowadays, they are present in the majority of commercial products directed to repair or regenerate damaged bone tissue. Finally, in the last few decades, they have been suggested and studied as drug delivering devices and as vehicles of DNA and RNA for the future generation therapies.

  19. Variability of nitrate and phosphate

    Digital Repository Service at National Institute of Oceanography (India)

    Sardessai, S.; Sundar, D.

    Nitrate and phosphate are important elements of the biogeochemical system of an estuary. Observations carried out during the dry season April-May 2002, and March 2003 and wet season September 2002, show temporal and spatial variability of these two...

  20. Preparation of calcium phosphate paste

    International Nuclear Information System (INIS)

    Mohd Reusmaazran Yusof; Norzita Yaacob; Idris Besar; Che Seman Mahmood; Rusnah Mustafa

    2010-01-01

    Calcium phosphate paste were prepared by mixing between calcium sodium potassium phosphate, Ca 2 NaK (PO 4 ) 2 (CSPP) and monocalcium phosphate monohydrate, Ca(H 2 PO 4 ) 2 .H 2 O (MCPM). CSPP were obtained by reaction between calcium hydrogen phosphate (CaHPO 4 ), potassium carbonate (K 2 CO 3 ) and sodium carbonate (Na 2 CO 3 ) in solid state sintering process followed by quenching in air at 1000 degree Celsius. The paste was aging in simulated body fluid (SBF) for 0.5, 1, 3, 6, 12, 24, 48 hrs, 3, 7 and 14 days. The morphological investigation indicated the formation of apatite crystal were first growth after 24 hours. The obvious growth of apatite crystal was shown at 3 days. The obvious growth of apatite crystal was shown in 7 and 14 days indicated the prediction of paste would have rapid reaction with bone after implantation. (author)

  1. Calcium phosphates for biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Canillas, M.; Pena, P.; Aza, A.H. de; Rodriguez, M.A.

    2017-07-01

    The history of calcium phosphates in the medicine field starts in 1769 when the first evidence of its existence in the bone tissue is discovered. Since then, the interest for calcium phosphates has increased among the scientific community. Their study has been developed in parallel with new advances in materials sciences, medicine or tissue engineering areas. Bone tissue engineering is the field where calcium phosphates have had a great importance. While the first bioceramics are selected according to bioinert, biocompatibility and mechanical properties with the aim to replace bone tissue damaged, calcium phosphates open the way to the bone tissue regeneration challenge. Nowadays, they are present in the majority of commercial products directed to repair or regenerate damaged bone tissue. Finally, in the last few decades, they have been suggested and studied as drug delivering devices and as vehicles of DNA and RNA for the future generation therapies. (Author)

  2. Phosphate solubilization and multiple plant growth promoting ...

    African Journals Online (AJOL)

    Phosphate solubilizing efficiencies of the strains were analyzed using different insoluble phosphorus sources and the results show that most isolates released a substantial amount of soluble phosphate from tricalcium phosphate, rock phosphate and bone meal. Screening for multiple plant growth promoting attributes ...

  3. Electrical properties of phosphate glasses

    International Nuclear Information System (INIS)

    Mogus-Milankovic, A; Santic, A; Reis, S T; Day, D E

    2009-01-01

    Investigation of the electrical properties of phosphate glasses where transition metal oxide such as iron oxide is the network former and network modifier is presented. Phosphate glasses containing iron are electronically conducting glasses where the polaronic conduction is due to the electron hopping from low to high iron valence state. The identification of structural defects caused by ion/polaron migration, the analysis of dipolar states and electrical conductivity in iron phosphate glasses containing various alkali and mixed alkali ions was performed on the basis of the impedance spectroscopy (IS). The changes in electrical conductivity from as-quenched phosphate glass to fully crystallized glass (glass-ceramics) by IS are analyzed. A change in the characteristic features of IS follows the changes in glass and crystallized glass network. Using IS, the contribution of glass matrix, crystallized grains and grain boundary to the total electrical conductivity for iron phosphate glasses was analyzed. It was shown that decrease in conductivity is caused by discontinuities in the conduction pathways as a result of the disruption of crystalline network where two or more crystalline phases are formed. Also, phosphate-based glasses offer a unique range of biomaterials, as they form direct chemical bonding with hard/soft tissue. The surface charges of bioactive glasses are recognized to be the most important factors in determining biological responses. The improved bioactivity of the bioactive glasses as a result of the effects of the surface charges generated by electrical polarization is discussed.

  4. The effect of farmyard manure and calcium ammonium nitrate ...

    African Journals Online (AJOL)

    The effect of farmyard manure and calcium ammonium nitrate fertilisers on micronutrient density (iron, zinc, manganese, calcium and potassium) and seed yields of solanium villosum (black nightshade) and cleome gynandra (cat whiskers) on uetric nitisol.

  5. Stability and Concentration Verification of Ammonium Perchlorate Dosing Solutions

    National Research Council Canada - National Science Library

    Tsui, David

    1998-01-01

    Stability and concentration verification was performed for the ammonium perchlorate dosing solutions used in the on-going 90-Day Oral Toxicity Study conducted by Springborn Laboratories, Inc. (SLI Study No. 3433.1...

  6. Study on Thorium Hidroxide and Ammonium Diuranate precipitation

    International Nuclear Information System (INIS)

    Damunir; Sukarsono, R; Busron-Masduki; Indra-Suryawan

    1996-01-01

    Thorium hydroxide and ammonium diuranate precipitation studied by the reaction of mixed thorium nitrate and uranyl nitrate using ammonium hydroxide. The purposes of this research was study of pH condition. U/Th ratio and NH 4 OH concentration on the precipitation. Mixed of thorium nitrate and uranyl nitrate 50 ml was reacted by excess ammonium hydroxide 2 - 10 M, pH 4-8, 40-80 o C of temperature and 5 - 100 % ratio of U/Th. The best of precipitation depend on thorium and uranium content on the precipitation. The experiment result for the best condition of precipitation was 25 % of ratio U/Th, pH 6 - 8, 60-80 o C of temperature, and 6 - 10 M concentration of ammonium hydroxide, was produced precipitate by 3,938 - 5,455 weight percent of mean concentration of U and 22,365-31,873 weight percent of mean concentration of Th

  7. The Effect of Phytase on the Oxygen Isotope Composition of Phosphate

    Science.gov (United States)

    von Sperber, C.; Tamburini, F.; Bernasconi, S. M.; Frossard, E.

    2013-12-01

    for acid phosphatases (6). In contrast, the results from assays with phytase from Aspergillus niger indicate that the exchange of oxygen occurs at more than one third of the total 24 oxygen which are associated to the phosphates in IP6. In addition, we observe a change in the oxygen isotope composition of Pi when using myo-inositol and potassium-dihydrogen-phosphate as sole substrates in the enzymatic assays with phytase from Aspergillus niger. These observations suggest that the reformation of IP6 from the two products of the reaction (myo-inositol and Pi) is taking place at a rate, which is within the time scale of the experiment. In this case, the isotopic fractionation caused by phytase from Aspergillus niger will be determined by the equilibrium of the reaction. Further experiments are in process to verify these findings.

  8. Study on the relation between uranium content and total phosphorus in some sudanese phosphate ore samples

    International Nuclear Information System (INIS)

    Eltayeb, M. A. H.; Mohammed, A. A.

    2003-01-01

    In the present work uranium content and total phosphorus were determined in 30 phosphate ore samples collected from Kurun and Uro areas in Nuba Mountains in Sudan. Spectrophotometry technique was used for this purpose. Uranium analysis is based on the use of nitrogen (V) acid for leaching the rock, and treatment with ammonium carbonate solution, whereby uranium (Vi) is kept in solution as its carbonate complex. The ion exchange technique was used for the recovery of uranium. Uranium was eluted from the resin with 1 M hydrochloric acid. In the elute, uranium was determined spectrophotometrically by measurement of absorbance of the yellow uranium (Vi)-8-hydroxyquinolate complex at λ 400 nm. The total phosphorus was measured as (P 2 O 5 %) by treatment of the total liquor with ammonium molybdate solution. The absorbance of the blue complex was measured at λ 880 nm. The results show that a limited relation is existed between uranium content and total phosphorus in phosphate samples from kurun area, which contain 58.8 ppm uranium in average, where there are no relation is existed in phosphate samples from uro area, which contain 200 ppm uranium in average. (Author)

  9. Study on the relation between uranium content and total phosphorus in some sudanese phosphate ore samples

    International Nuclear Information System (INIS)

    Mohammed, A.A.; Eltayeb, M.A.H.

    2003-01-01

    In the present work uranium content and total phosphorous were determined in 30 phosphate ore samples collected from Kurun and Uro areas in Nuba mountains in sudan. Spectrophotometry technique was used for this purpose. Uranium analysis is based on the use of nitrogen (V) acid for leaching the rock, and treatment with ammonium carbonate solution, whereby uranium (VI) is kept in solution as its carbonate complex. The ion-exchange technique was used for the recovery of uranium. Uranium was eluted from the resin with 1 M hydrochloric acid. In the elute, uranium was determined spectrophotometrically by measurement of the absorbance of the yellow uranium (VI) - 8- hydroxyquinolate complex at λ 400 nm. The total phosphorus was measured as (P 2 O 5 %) by treatment of the leach liquor with ammonium molybdate solution. The absorbance of the blue complex was measured at λ 880 nm. The results show that a limited relation is existed between uranium content and total phosphorus in phosphate samples from Kurun area, which contain 58.8 ppm uranium in average, where there are no relation is existed in phosphate samples samples from Uro area, which contain 200 ppm uranium in average

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

    Energy Technology Data Exchange (ETDEWEB)

    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.

  11. Burning characteristics of ammonium nitrate-based composite propellants supplemented with ammonium dichromate

    Energy Technology Data Exchange (ETDEWEB)

    Kohga, Makoto; Nishino, Saeko [Department of Applied Chemistry, National Defense Academy, Yokosuka, Kanagawa 239-8686 (Japan)

    2009-08-15

    Ammonium nitrate (AN)-based composite propellants have attracted much attention, primarily because of the clean burning nature of AN as an oxidizer. However, such propellants have some disadvantages such as poor ignition and low burning rate. Ammonium dichromate (ADC) is used as a burning catalyst for AN-based propellants; however, the effect of ADC on the burning characteristics has yet to be sufficiently delineated. The burning characteristics of AN/ADC propellants prepared with various contents of AN and ADC have been investigated in this study. The theoretical performance of an AN-based propellant is improved by the addition of ADC. The increase in the burning rate is enhanced and the pressure deflagration limit (PDL) becomes lower with increasing amount of ADC added. The increasing ratio of the burning rate with respect to the amount of ADC is independent of the AN content and the combustion pressure. The optimal amount of ADC for improving the burning characteristics has been determined. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  12. Mutagenicity of quaternary ammonium salts containing carbohydrate moieties

    Energy Technology Data Exchange (ETDEWEB)

    Dmochowska, Barbara [Department of Carbohydrate Chemistry, University of Gdansk, Sobieskiego 18, 80-952 Gdansk (Poland); Piosik, Jacek; Woziwodzka, Anna [Intercollegiate Faculty of Biotechnology, University of Gdansk and Medical University of Gdansk, Kladki 24, 80-822 Gdansk (Poland); Sikora, Karol; Wisniewski, Andrzej [Department of Carbohydrate Chemistry, University of Gdansk, Sobieskiego 18, 80-952 Gdansk (Poland); Wegrzyn, Grzegorz, E-mail: wegrzyn@biotech.univ.gda.pl [Department of Molecular Biology, University of Gdansk, Kladki 24, 80-822 Gdansk (Poland)

    2011-10-15

    Highlights: {yields} A series of quaternary ammonium salts containing carbohydrate moieties, with configuration D-galacto, D-gluco and D-manno, was synthesized and characterized. {yields} The quaternary ammonium salts containing carbohydrate moieties revealed potent mutagenic activities, as assessed by using the Vibrio harveyi bioluminescence mutagenicity test. {yields} The N-[2-(D-glycopyranosyloxy)ethyl]-N,N,N-trimethylaminium salts were of the highest activity in the mutagenicity assay. {yields} We suggest that quaternary ammonium salts may be more hazardous than previously supposed. - Abstract: Quaternary ammonium salts are widely used in industrial, agricultural, healthcare and domestic applications. They are believed to be safe compounds, with little or no health hazard to humans. However, in this report, we demonstrate that a series of newly synthesized quaternary ammonium salts containing carbohydrate moieties reveal potent mutagenic activities, as assessed by using the Vibrio harveyi bioluminescence mutagenicity test. D-Gluco- and D-galacto-derivatives were found to have a higher mutagenic potential than D-manno-derivatives. Among the former groups of compounds, the N-[2-(D-glycopyranosyloxy)ethyl]-N,N,N-trimethylaminium salts were of the highest activity in the mutagenicity assay. These results suggest that the safety of quaternary ammonium salts may be lower than previously supposed, indicating a need for testing such compounds for their mutagenicity.

  13. Ammonium as sole N source improves grain quality in wheat.

    Science.gov (United States)

    Fuertes-Mendizábal, Teresa; González-Torralba, Jon; Arregui, Luis M; González-Murua, Carmen; González-Moro, M Begoña; Estavillo, José M

    2013-07-01

    The skilful handling of N fertilizer, including N source type and its timing, is necessary to obtain maximum profitability in wheat crops in terms of production and quality. Studies on grain yield and quality with ammonium as sole N source have not yet been conducted. The aim of this study was to evaluate the effect of N source management (nitrate vs. ammonium), and splitting it into two or three amendments during the wheat life cycle, on grain yield and quality under irrigated conditions. This experiment demonstrates that Cezanne wheat plants growing with ammonium as exclusive N source are able to achieve the same yield as plants growing with nitrate and that individual wheat plants grown in irrigated pots can efficiently use late N applied in GS37. Ammonium nutrition increased both types of grain reserve proteins (gliadins and glutenins) and also increased the ratio gli/glu with respect to nitrate nutrition. The splitting of the N rate enhanced the ammonium effect on grain protein composition. The application of ammonium N source, especially when split into three amendments, has an analogous effect on grain protein content and composition to applications at a higher N rate, leading to higher N use efficiency. © 2012 Society of Chemical Industry.

  14. Mutagenicity of quaternary ammonium salts containing carbohydrate moieties

    International Nuclear Information System (INIS)

    Dmochowska, Barbara; Piosik, Jacek; Woziwodzka, Anna; Sikora, Karol; Wisniewski, Andrzej; Wegrzyn, Grzegorz

    2011-01-01

    Highlights: → A series of quaternary ammonium salts containing carbohydrate moieties, with configuration D-galacto, D-gluco and D-manno, was synthesized and characterized. → The quaternary ammonium salts containing carbohydrate moieties revealed potent mutagenic activities, as assessed by using the Vibrio harveyi bioluminescence mutagenicity test. → The N-[2-(D-glycopyranosyloxy)ethyl]-N,N,N-trimethylaminium salts were of the highest activity in the mutagenicity assay. → We suggest that quaternary ammonium salts may be more hazardous than previously supposed. - Abstract: Quaternary ammonium salts are widely used in industrial, agricultural, healthcare and domestic applications. They are believed to be safe compounds, with little or no health hazard to humans. However, in this report, we demonstrate that a series of newly synthesized quaternary ammonium salts containing carbohydrate moieties reveal potent mutagenic activities, as assessed by using the Vibrio harveyi bioluminescence mutagenicity test. D-Gluco- and D-galacto-derivatives were found to have a higher mutagenic potential than D-manno-derivatives. Among the former groups of compounds, the N-[2-(D-glycopyranosyloxy)ethyl]-N,N,N-trimethylaminium salts were of the highest activity in the mutagenicity assay. These results suggest that the safety of quaternary ammonium salts may be lower than previously supposed, indicating a need for testing such compounds for their mutagenicity.

  15. Fabrication of a Biomass-Based Hydrous Zirconium Oxide Nanocomposite for Preferable Phosphate Removal and Recovery.

    Science.gov (United States)

    Qiu, Hui; Liang, Chen; Zhang, Xiaolin; Chen, Mindong; Zhao, Yunxia; Tao, Tao; Xu, Zhengwen; Liu, Gang

    2015-09-23

    Advanced removal of phosphate by low-cost adsorbents from municipal wastewater or industrial effluents is an effective and economic way to prevent the occurrence of eutrophication. Here, we proposed a novel method to immobilize hydrous zirconium oxide nanoparticle within quaternary-aminated wheat straw, and obtained an inexpensive, eco-friendly nanocomposite Ws-N-Zr. The biomass-based Ws-N-Zr exhibited higher preference toward phosphate than commercial anion exchanger IRA-900 when competing sulfate ions coexisted at relatively high levels. Such excellent performance of Ws-N-Zr resulted from its specific hybrid structure, the quaternary ammonium groups bonded on the host favor the preconcentration of phosphate ions inside the wheat straw based on Donnan effect, and the encapsulated HZO nanoparticle exhibits preferable sequestration of phosphate ions through specific interaction, as further demonstrated by FTIR and X-ray photoelectron spectroscopy. Cycle adsorption and regeneration experiments demonstrated that Ws-N-Zr could be employed for repeated use without significant capacity loss, when the binary NaOH-NaCl solution was employed as the regenerant. The influence of solution pH and contact time was also examined. The results suggested that Ws-N-Zr has a great potential in efficient removal of phosphate in contaminated waters.

  16. The effect of environmental conditions and soil physicochemistry on phosphate stabilisation of Pb in shooting range soils.

    Science.gov (United States)

    Sanderson, Peter; Naidu, Ravi; Bolan, Nanthi

    2016-04-01

    The stabilisation of Pb in the soil by phosphate is influenced by environmental conditions and physicochemical properties of the soils to which it is applied. Stabilisation of Pb by phosphate was examined in four soils under different environmental conditions. The effect of soil moisture and temperature on stabilisation of Pb by phosphate was examined by measurement of water extractable and bioaccessible Pb, sequential fractionation and X-ray absorption spectroscopy. The addition of humic acid, ammonium nitrate and chloride was also examined for inhibition or improvement of Pb stability with phosphate treatment. The effect of moisture level varied between soils. In soil MB and DA a soil moisture level of 50% water holding capacity was sufficient to maximise stabilisation of Pb, but in soil TV and PE reduction in bioaccessible Pb was inhibited at this moisture level. Providing moisture at twice the soil water holding capacity did not enhance the effect of phosphate on Pb stabilisation. The difference of Pb stability as a result of incubating phosphate treated soils at 18 °C and 37 °C was relatively small. However wet-dry cycles decreased the effectiveness of phosphate treatment. The reduction in bioaccessible Pb obtained was between 20 and 40% with the most optimal treatment conditions. The reduction in water extractable Pb by phosphate was substantial regardless of incubation conditions and the effect of different temperature and soil moisture regimes was not significant. Selective sequential extraction showed phosphate treatment converted Pb in fraction 1 (exchangeable, acid and water soluble) to fraction 2 (reducible). There were small difference in fraction 4 (residual) Pb and fraction 1 as a result of treatment conditions. X-ray absorption spectroscopy of stabilised PE soil revealed small differences in Pb speciation under varying soil moisture and temperature treatments. The addition of humic acid and chloride produced the greatest effect on Pb speciation in

  17. Use of Ferrihydrite-Coated Pozzolana and Biogenic Green Rust to Purify Waste Water Containing Phosphate and Nitrate

    Energy Technology Data Exchange (ETDEWEB)

    Ruby, Christian; Naille, Sébastien; Ona-Nguema, Georges; Morin, Guillaume; Mallet, Martine; Guerbois, Delphine; Barthélémy, Kévin; Etique, Marjorie; Zegeye, Asfaw; Zhang, Yuhai; Boumaïza, Hella; Al-Jaberi, Muayad; Renard, Aurélien; Noël, Vincent; Binda, Paul; Hanna, Khalil; Despas, Christelle; Abdelmoula, Mustapha; Kukkadapu, Ravi; Sarrias, Joseph; Albignac, Magali; Rocklin, Pascal; Nauleau, Fabrice; Hyvrard, Nathalie; Génin, Jean-Marie

    2016-06-27

    The activated sludge treatments combined to the addition of ferric chloride is commonly used to eliminate nitrate and phosphate from waste water in urban area. These processes that need costly infrastructures are not suitable for rural areas and passive treatments (lagoons, reed bed filters…) are more frequently performed. Reed bed filters are efficient for removing organic matter but are not suitable for treating phosphate and nitrate as well. Passive water treatments using various materials (hydroxyapatite, slag…) were already performed, but those allowing the elimination of both nitrate and phosphate are not actually available. The goal of this work is to identify the most suitable iron based materials for such treatments and to determine their optimal use conditions, in particular in hydrodynamic mode. The reactivity of the iron based minerals was measured either by using free particles in suspension or by depositing these particles on a solid substrate. Pouzzolana that is characterized by a porous sponge-like structure suits for settling a high amount of iron oxides. The experimental conditions enabling to avoid any ammonium formation when green rust encounters nitrate were determined within the framework of a full factorial design. The process is divided into two steps that will be performed inside two separated reactors. Indeed, the presence of phosphate inhibits the reduction of nitrate by green rust and the dephosphatation process must precede the denitrification process. In order to remove phosphate, ferrihydrite coated pouzzolana is the best materials. The kinetics of reaction of green rust with nitrate is relatively slow and often leads to the formation of ammonium. The recommendation of the identified process is to favor the accumulation of nitrite in a first step, these species reacting much more quickly with green rust and do not transform into ammonium.

  18. The precipitation of magnesium potassium phosphate hexahydrate for P and K recovery from synthetic urine.

    Science.gov (United States)

    Xu, Kangning; Li, Jiyun; Zheng, Min; Zhang, Chi; Xie, Tao; Wang, Chengwen

    2015-09-01

    Nutrients recovery from urine to close the nutrient loop is one of the most attractive benefits of source separation in wastewater management. The current study presents an investigation of the thermodynamic modeling of the recovery of P and K from synthetic urine via the precipitation of magnesium potassium phosphate hexahydrate (MPP). Experimental results show that maximum recovery efficiencies of P and K reached 99% and 33%, respectively, when the precipitation process was initiated only through adding dissolvable Mg compound source. pH level and molar ratio of Mg:P were key factors determining the nutrient recovery efficiencies. Precipitation equilibrium of MPP and magnesium sodium phosphate heptahydrate (MSP) was confirmed via precipitates analysis using a Scanning Electron Microscope/Energy Dispersive Spectrometer and an X-ray Diffractometer. Then, the standard solubility products of MPP and MSP in the synthetic urine were estimated to be 10(-12.2 ± 0.0.253) and 10(-11.6 ± 0.253), respectively. The thermodynamic model formulated on chemical software PHREEQC could well fit the experimental results via comparing the simulated and measured concentrations of K and P in equilibrium. Precipitation potentials of three struvite-type compounds were calculated through thermodynamic modeling. Magnesium ammonium phosphate hexahydrate (MAP) has a much higher tendency to precipitate than MPP and MSP in normal urine while MSP was the main inhibitor of MPP in ammonium-removed urine. To optimize the K recovery, ammonium should be removed prior as much as possible and an alternative alkaline compound should be explored for pH adjustment rather than NaOH. Copyright © 2015 Elsevier Ltd. All rights reserved.

  19. Ammonium Transformation in 14 Lakes along a Trophic Gradient

    Directory of Open Access Journals (Sweden)

    Barbara Leoni

    2018-03-01

    Full Text Available Ammonia is a widespread pollutant in aquatic ecosystems originating directly and indirectly from human activities, which can strongly affect the structure and functioning of the aquatic foodweb. The biological oxidation of NH4+ to nitrite, and then nitrate is a key part of the complex nitrogen cycle and a fundamental process in aquatic environments, having a profound influence on ecosystem stability and functionality. Environmental studies have shown that our current knowledge of physical and chemical factors that control this process and the abundance and function of involved microorganisms are not entirely understood. In this paper, the efficiency and the transformation velocity of ammonium into oxidised compounds in 14 south-alpine lakes in northern Italy, with a similar origin, but different trophic levels, are compared with lab-scale experimentations (20 °C, dark, oxygen saturation that are performed in artificial microcosms (4 L. The water samples were collected in different months to highlight the possible effect of seasonality on the development of the ammonium oxidation process. In four-liter microcosms, concentrations were increased by 1 mg/L NH4+ and the process of ammonium oxidation was constantly monitored. The time elapsed for the decrease of 25% and 95% of the initial ion ammonium concentration and the rate for that ammonium oxidation were evaluated. Principal Component Analysis and General Linear Model, performed on 56 observations and several chemical and physical parameters, highlighted the important roles of total phosphorus and nitrogen concentrations on the commencement of the oxidation process. Meanwhile, the natural concentration of ammonium influenced the rate of nitrification (µg NH4+/L day. Seasonality did not seem to significantly affect the ammonium transformation. The results highlight the different vulnerabilities of lakes with different trophic statuses.

  20. Ammonium inhibition of nitrogenase activity in Herbaspirillum seropedicae

    Energy Technology Data Exchange (ETDEWEB)

    Fu, H.; Burris, R.H. (Univ. of Wisconsin, Madison (USA))

    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.

  1. Development of Polymethylmethacrylate Based Composite for Gas Sensing Application

    Directory of Open Access Journals (Sweden)

    S. Devikala

    2011-01-01

    Full Text Available Gas detection instruments are increasingly needed for industrial health and safety, environmental monitoring and process control. Conductive polymer composites have various industrial applications. The composite prepared by mixing carbon black with polymethylmethacrylate (PMMA has very good gas sensing applications. The gas sensors based on carbon nanotube/polymer, ceramic and metal oxide composites such as epoxy, polyimide, PMMA / Barium titanate and tin oxide have also been developed. In the present work, a new composite has been prepared by using PMMA and ammonium dihydrogen phosphate (ADP. The PMMA/Ammonium dihydrogen phosphate (PMADP composites PMADP 1 and PMADP 2 were characterized by using Powder XRD. The thick films of the composite on glass plates were prepared by using a spin coating unit at 9000 rpm. The application of the thick film as gas sensor has been studied between 0 and 2000 seconds. The results reveal that the thick film of PMADP composite can function as a very good gas sensor.

  2. Reaction Mechanisms of Magnesium Potassium Phosphate Cement and its Application

    Science.gov (United States)

    Qiao, Fei

    Magnesium potassium phosphate cement (MKPC) is a kind of cementitious binder in which the chemical bond is formed via a heterogeneous acid-base reaction between dead burned magnesia powder and potassium phosphate solution at room temperature. Small amount of boron compounds can be incorporated in the cement as a setting retarder. The final reaction product of MgO-KH2PO4-H 2O ternary system is identified as magnesium potassium phosphate hexahydrate, MgKPO4·6H2O. However, the mechanisms and procedures through which this crystalline product is formed and the conditions under which the crystallization process would be influenced are not yet clear. Understanding of the reaction mechanism of the system is helpful for developing new methodologies to control the rapid reaction process and furthermore, to adjust the phase assemblage of the binder, and to enhance the macroscopic properties. This study is mainly focused on the examination of the reaction mechanism of MKPC. In addition, the formulation optimization, microstructure characterization and field application in rapid repair are also systematically studied. The chemical reactions between magnesia and potassium dihydrogen phosphate are essentially an acid-base reaction with strong heat release, the pH and temperature variation throughout the reaction process could provide useful information to disclose the different stages in the reaction. However, it would be very difficult to conduct such tests on the cement paste due to the limited water content and fast setting. In the current research, the reaction mechanism of MKPC is investigated on the diluted MKPC system through monitoring the pH and temperature development, identification of the solid phase formed, and measurement of the ionic concentration of the solution. The reaction process can be explained as follows: when magnesia and potassium phosphate powder are mixed with water, phosphate is readily dissolved, which is instantly followed by the dissociation of

  3. Dynamics and diversity of phosphate mineralizing bacteria in the coral reefs of Gulf of Mannar

    Digital Repository Service at National Institute of Oceanography (India)

    Kannapiran, E.; Ravindran, J.

    .2g, Ammonium sulphate 0.5g, Magnesium sulphate 0.1g, Potassium chloride 0.2g, Dextrose 10g, Soil extract 200ml, Distilled water 800ml, Trace element 1ml, Agar 18g and pH 7.2±0.1) [11] was used for the enumeration of Inorganic Phosphate Solubilizing... The biological decomposition of organic phosphorus in the marine environment is considered as the result of bacterial action and rate of decomposition of organic phosphorus by bacteria depend on the density of the phosphatase producing bacterial population [14...

  4. Uranium endowments in phosphate rock

    International Nuclear Information System (INIS)

    Ulrich, Andrea E.; Schnug, Ewald; Prasser, Horst-Michael; Frossard, Emmanuel

    2014-01-01

    This study seeks to identify and specify the components that make up the prospects of U recovery from phosphate rock. A systems approach is taken. The assessment includes i) reviewing past recovery experience and lessons learned; ii) identifying factors that determine recovery; and iii) establishing a contemporary evaluation of U endowments in phosphate rock reserves, as well as the available and recoverable amounts from phosphate rock and phosphoric acid production. We find that in the past, recovery did not fulfill its potential and that the breakup of the Soviet Union worsened then-favorable recovery market conditions in the 1990s. We find that an estimated 5.7 million tU may be recoverable from phosphate rock reserves. In 2010, the recoverable tU from phosphate rock and phosphoric acid production may have been 15,000 tU and 11,000 tU, respectively. This could have filled the world U supply-demand gap for nuclear energy production. The results suggest that the U.S., Morocco, Tunisia, and Russia would be particularly well-suited to recover U, taking infrastructural considerations into account. We demonstrate future research needs, as well as sustainability orientations. We conclude that in order to promote investment and production, it seems necessary to establish long-term contracts at guaranteed prices, ensuring profitability for phosphoric acid producers. - Highlights: • We identify components that underlie the recovery of uranium from phosphate rock. • We estimate that 11,000 tU may have been recoverable from phosphoric acid in 2010. • Recovery is a resource conservation and environmental pollution control strategy. • To ensure investment in recovery technology, profitability needs to be secured

  5. Uranium endowments in phosphate rock

    Energy Technology Data Exchange (ETDEWEB)

    Ulrich, Andrea E., E-mail: andrea.ulrich@env.ethz.ch [Institute for Environmental Decisions (IED), Natural and Social Science Interface, ETH Zurich Universitässtrasse 22, 8092 Zurich (Switzerland); Institute for Agricultural Sciences, Plant Nutrition, ETH Zurich, Eschikon 33, 8315 Lindau (Switzerland); Schnug, Ewald, E-mail: e.schnug@tu-braunschweig.de [Department of Life Sciences, Technical University of Braunschweig, Pockelsstraße 14, D-38106 Braunschweig (Germany); Prasser, Horst-Michael, E-mail: prasser@lke.mavt.ethz.ch [Institute of Energy Technology, Laboratory of Nuclear Energy Systems, ETH Zurich, Sonneggstrasse 3, 8092 Zurich (Switzerland); Frossard, Emmanuel, E-mail: emmanuel.frossard@usys.ethz.ch [Institute for Agricultural Sciences, Plant Nutrition, ETH Zurich, Eschikon 33, 8315 Lindau (Switzerland)

    2014-04-01

    This study seeks to identify and specify the components that make up the prospects of U recovery from phosphate rock. A systems approach is taken. The assessment includes i) reviewing past recovery experience and lessons learned; ii) identifying factors that determine recovery; and iii) establishing a contemporary evaluation of U endowments in phosphate rock reserves, as well as the available and recoverable amounts from phosphate rock and phosphoric acid production. We find that in the past, recovery did not fulfill its potential and that the breakup of the Soviet Union worsened then-favorable recovery market conditions in the 1990s. We find that an estimated 5.7 million tU may be recoverable from phosphate rock reserves. In 2010, the recoverable tU from phosphate rock and phosphoric acid production may have been 15,000 tU and 11,000 tU, respectively. This could have filled the world U supply-demand gap for nuclear energy production. The results suggest that the U.S., Morocco, Tunisia, and Russia would be particularly well-suited to recover U, taking infrastructural considerations into account. We demonstrate future research needs, as well as sustainability orientations. We conclude that in order to promote investment and production, it seems necessary to establish long-term contracts at guaranteed prices, ensuring profitability for phosphoric acid producers. - Highlights: • We identify components that underlie the recovery of uranium from phosphate rock. • We estimate that 11,000 tU may have been recoverable from phosphoric acid in 2010. • Recovery is a resource conservation and environmental pollution control strategy. • To ensure investment in recovery technology, profitability needs to be secured.

  6. Lithium increases ammonium excretion leading to altered urinary acid-base buffer composition.

    Science.gov (United States)

    Trepiccione, Francesco; Altobelli, Claudia; Capasso, Giovambattista; Christensen, Birgitte Mønster; Frische, Sebastian

    2017-11-24

    Previous reports identify a voltage dependent distal renal tubular acidosis (dRTA) secondary to lithium (Li + ) salt administration. This was based on the inability of Li + -treated patients to increase the urine-blood (U-B) pCO 2 when challenged with NaHCO 3 and, the ability of sodium neutral phosphate or Na 2 SO 4 administration to restore U-B pCO 2 in experimental animal models. The underlying mechanisms for the Li + -induced dRTA are still unknown. To address this point, a 7 days time course of the urinary acid-base parameters was investigated in rats challenged with LiCl, LiCitrate, NaCl, or NaCitrate. LiCl induced the largest polyuria and a mild metabolic acidosis. Li + -treatment induced a biphasic response. In the first 2 days, proper urine volume and acidification occurred, while from the 3rd day of treatment, polyuria developed progressively. In this latter phase, the LiCl-treated group progressively excreted more NH 4 + and less pCO 2 , suggesting that NH 3 /NH 4 + became the main urinary buffer. This physiological parameter was corroborated by the upregulation of NBCn1 (a marker of increased ammonium recycling) in the inner stripe of outer medulla of LiCl treated rats. Finally, by investigating NH 4 + excretion in ENaC-cKO mice, a model resistant to Li + -induced polyuria, a primary role of the CD was confirmed. By definition, dRTA is characterized by deficient urinary ammonium excretion. Our data question the presence of a voltage-dependent Li + -induced dRTA in rats treated with LiCl for 7 days and the data suggest that the alkaline urine pH induced by NH 3 /NH 4 + as the main buffer has lead to the interpretation dRTA in previous studies.

  7. Reuse of ammonium fluoride generated in the uranium hexafluoride conversion

    International Nuclear Information System (INIS)

    Silva Neto, J.B.; Carvalho, E.F. Urano de; Durazzo, M.; Riella, H.G

    2010-01-01

    The Nuclear Fuel Centre of IPEN / CNEN - SP develops and manufactures dispersion fuel with high uranium concentration to meet the demand of the IEA-R1 reactor and future research reactors planned to be constructed in Brazil. The fuel uses uranium silicide (U 3 Si 2 ) dispersed in aluminum. For producing the fuel, the processes for uranium hexafluoride (UF 6 ) conversion consist in obtaining U 3 Si 2 and / or U 3 O 8 through the preparation of intermediate compounds, among them ammonium uranyl carbonate - AUC, ammonium diuranate - DUA and uranium tetrafluoride - UF 4 . This work describes a procedure for preparing uranium tetrafluoride by a dry route using as raw material the filtrate generated when producing routinely ammonium uranyl carbonate. The filtrate consists primarily of a solution containing high concentrations of ammonium (NH 4 + ), fluoride (F - ), carbonate (CO 3 -- ) and low concentrations of uranium. The procedure is basically the recovery of NH 4 F and uranium, as UF 4 , through the crystallization of ammonium bifluoride (NH 4 HF 2 ) and, in a later step, the addition of UO 2 , occurring fluoridation and decomposition. The UF 4 obtained is further diluted in the UF 4 produced routinely at IPEN / CNEN-SP by a wet route process. (author)

  8. Electrospray ionization tandem mass spectrometry of ammonium cationized polyethers.

    Science.gov (United States)

    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. © American Society for Mass Spectrometry, 2011

  9. Spectrophotometric determination of trace uranium in phosphate ore samples from kurum and uro areas, Nuba mountains, Sudan

    International Nuclear Information System (INIS)

    Mohamed, A. A.; Ali, A. H.; Altayeb, M. A. H.

    2004-01-01

    A method was proposed for the spectrophotometric determination of uranium content in phosphate ores. the method is based on the use of nitrogen (v) acid for leaching the rock, and treatment with ammonium carbonate solution, whereby uranium (Vi) is kept in solution as its carbonate complex. The ion-exchange technique was used for the recovery of uranium. Uranium was determined spectrophotometrically by measurement of the absorbance of the yellow uranium (Vi)-8-hydroxyquinolate complex at λ 425 nm. The procedure was used for the determination of trace uranium content in 30 phosphate ore samples collected from Kurun and Uro areas in Nuba mountains in Sudan. X-ray fluorescence technique was employed for the assessment of the method used. The spectrophotometric method results show a high similarity with those obtained by XRF technique. This agreement indicates that the procedure proposed here has been successfully applied for the determination of uranium in phosphate ores. (Author)

  10. Dielectric, thermal and mechanical properties of ADP doped PVA composites

    Science.gov (United States)

    Naik, Jagadish; Bhajantri, R. F.; Ravindrachary, V.; Rathod, Sunil G.; Sheela, T.; Naik, Ishwar

    2015-06-01

    Polymer composites of poly(vinyl alcohol) (PVA), doped with different concentrations of ammonium dihydrogen phosphate (ADP) has been prepared by solution casting. The formation of complexation between ADP and PVA was confirmed with the help of Fourier transforms infrared (FTIR) spectroscopy. Thermogravimetric analysis (TGA) shows thermal stability of the prepared composites. Impedance analyzer study revealed the increase in dielectric constant and loss with increase the ADP concentration and the strain rate of the prepared composites decreases with ADP concentration.

  11. Phosphorus release from phosphate rock and iron phosphate by low-molecular-weight organic acids.

    Science.gov (United States)

    Xu, Ren-kou; Zhu, Yong-guan; Chittleborough, David

    2004-01-01

    Low-molecular-weight(LMW) organic acids widely exist in soils, particularly in the rhizosphere. A series of batch experiments were carried out to investigate the phosphorus release from rock phosphate and iron phosphate by low-molecular-weight organic acids. Results showed that citric acid had the highest capacity to solubilize P from both rock and iron phosphate. P solubilization from rock phosphate and iron phosphate resulted in net proton consumption. P release from rock phosphate was positively correlated with the pKa values. P release from iron phosphate was positively correlated with Fe-organic acid stability constants except for aromatic acids, but was notcorrelated with pKa. Increase in the concentrations of organic acids enhanced P solubilization from both rock and iron phosphate almost linearly. Addition of phenolic compounds further increased the P release from iron phosphate. Initial solution pH had much more substantial effect on P release from rock phosphate than from iron phosphate.

  12. Habit modification of nearly perfect single crystals of potassium dihydrogen phosphate (KDP) by trivalent manganese ions studied using synchrotron radiation X-ray multiple diffraction in Renninger scanning mode

    OpenAIRE

    Lai, X; Roberts, KJ; Avanci, LH; Cardoso, LP; Sasaki, JM

    2003-01-01

    The X-ray multiple diffraction technique using synchrotron radiation is applied in the preliminary study of the habit modification of KDP samples as induced by incorporation of the trivalent transition metal cation Mn3+. High-resolution Renninger scans of pure and doped KDP were carried out using 400 as the primary reflection, echoing the fact that these impurity species were segregated in the {100} growth sector. The analysis of the Renninger scans of the doped KDP crystals is consistent wit...

  13. Bone mineral response to ammonium sulphate offered as a lick supplement in beef calves

    Directory of Open Access Journals (Sweden)

    L.E. Motsei

    2006-06-01

    Full Text Available Sixteen Bonsmara calves (4 males, 12 females between 10 and 18 months of age were blocked according to age and sex and randomly assigned to 2 groups. They were offered licks containing bone meal and salt (50:50 ratio (control and bone meal and ammonium sulphate (NH4SO4 at 1.25, 2.5, 5, 10, 15, and 18 % (treatment to evaluate the effects of dietary anions on bone phosphate (P concentration. Bone P concentration was significantly (P<0.05 higher in the NH4SO4 group compared with the control group, indicating that NH4SO4 was able to increase the P content of bone at each of the 6 concentrations used in the lick relative to the control animals, thereby improving the P status of the animals. Ammonium sulphate at 15% and 18% in the lick also significantly (P <0.05 increased bone P compared with the lower concentrations of NH4SO4. Bone calcium (Ca fluctuated as a result of the acidogenic lick. There was absorption of Ca when P was being resorbed and resorption of Ca when P was being absorbed into and out of bone. Bone Ca:P ratio ranged from 3.2 to 6.4 among the control group and 1.6 to 4.3 among the treatment group. Animals receiving the acidogenic lick had a higher percentage ash compared to the control group for most of the experimental period. Bone magnesium (Mg fluctuated in response to the acidogenic lick, and it was difficult to show a relationship between bone Mg and Ca or P. The overall mean cortical bone thickness was significantly (P < 0.05 greater in treatment (1.60 mm compared with control (1.43 mm calves and this was also true at sampling periods 2, 4, 5 and 6. Bone thickness followed bone P and not bone Ca. Results from this research indicate that the addition of ammonium sulphate to a lick had a beneficial effect in improving the P status by increasing bone P and improving the mineral status of bone by increasing the thickness of cortical bone and percentage ash.

  14. Properties of the ammonium tartrate/EPR dosimeter

    International Nuclear Information System (INIS)

    Yordanov, N.D.; Gancheva, V.

    2004-01-01

    The EPR response of γ-irradiated ammonium tartrate on the absorbed dose of γ-rays up to 22 kGy as well as the changes in the shape of the EPR spectrum upon applied modulation amplitude and microwave power are reported. Also the possibility to use ammonium tartrate together with Mn 2+ magnetically diluted in MgO as an internal reference material is evaluated. The influence of the microwave power and the modulation amplitude on their dose response is investigated. The results show that the radiation-induced EPR spectrum of ammonium tartrate, obtained at a low microwave power is complex consisting several patterns and is more easily saturated than the Mn 2+ EPR spectrum. In this case the following settings of the EPR parameters are recommended: H mod ≤0.05 mT and 10≤P MW ≤13 mW. Using these parameters the dosimeters can be considered for use in intercomparisons

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

    International Nuclear Information System (INIS)

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

    2013-01-01

    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)

  16. Rocket Solid Propellant Alternative Based on Ammonium Dinitramide

    Directory of Open Access Journals (Sweden)

    Grigore CICAN

    2017-03-01

    Full Text Available Due to the continuous run for a green environment the current article proposes a new type of solid propellant based on the fairly new synthesized oxidizer, ammonium dinitramide (ADN. Apart of having a higher specific impulse than the worldwide renowned oxidizer, ammonium perchlorate, ADN has the advantage, of leaving behind only nitrogen, oxygen and water after decomposing at high temperatures and therefore totally avoiding the formation of hydrogen chloride fumes. Based on the oxidizer to fuel ratios of the current formulations of the major rocket solid booster (e.g. Space Shuttle’s SRB, Ariane 5’s SRB which comprises mass variations of ammonium perchlorate oxidizer (70-75%, atomized aluminum powder (10-18% and polybutadiene binder (12-20% a new solid propellant was formulated. As previously stated, the new propellant formula and its variations use ADN as oxidizer and erythritol tetranitrate as fuel, keeping the same polybutadiene as binder.

  17. Temperature rising characteristics of ammonium diurante in microwave fields

    International Nuclear Information System (INIS)

    Liu Bingguo; Peng JinHui; Huang Daifu; Zhang Libo; Hu Jinming; Zhuang Zebiao; Kong Dongcheng; Guo Shenghui; Li Chunxiang

    2010-01-01

    The temperature rising characteristics of ammonium diurante, triuranium octaoxide (U 3 O 8 ), and their mixture were investigated under microwave irradiation, aiming at exploring newly theoretical foundation for advanced metallurgical methods. The temperature rising curves showed that ammonium diurante had weak capability to absorb microwave energy, while triuranium octaoxide had the very strong absorption capability. The temperature of mixture containing 20% of U 3 O 8 could rise from room temperature to 1171 K within 280 s. The ability to absorb microwave energy for the mixture with different ratios increased with the increase in the amount of U 3 O 8 . These are in good agreement with the results of Maxwell-Garnett effective medium theory. It is feasible to calcine ammonium diurante by adding of small amounts of U 3 O 8 in microwave fields.

  18. Investigation of alternative phosphating treatments for nickel and hexavalent chromium elimination

    International Nuclear Information System (INIS)

    Jazbinsek, Luiz Antonio Rossi

    2014-01-01

    The phosphating processes are widely used in industry as surface treatments for metals, especially for low thickness plates, improving the adhesion between the metallic surface and the paint coating, and increasing the durability of paint systems against corrosion attacks. The tricationic phosphates containing zinc, nickel and manganese are commonly applied on steel. There is much discussion about the replacement of nickel by another element in order to have an environmentally friendly phosphating process. Niobium as a replacement for nickel has been evaluated. The most significant environmental impacts of phosphating processes are related to the presence of nickel and hexavalent chromium used in the process, this last as a passivation treatment. Nickel and hexavalent chromium are harmful to human and environment leading to contamination of water and soil. In the present study phosphate layers containing zinc, manganese and niobium have been evaluated and characterized on galvanized steel, and the results were compared with phosphates containing zinc, manganese and nickel, or a bicationic phosphate layer with zinc and manganese. Although the use of hexavalent chromium is not recommended worldwide, it is still used in processes for sealing the porosity of phosphate layers. This element is carcinogenic and has been associated with various diseases. Due to the passivation characteristics of niobium, this study also evaluated the tricationic bath containing niobium ammonium oxalate as a passivation treatment. The results showed that it could act as a replacement for the hexavalent chromium. The results of the present study showed that formulations containing niobium are potential replacements for hexavalent chromium and similar corrosion protection was obtained for the phosphate containing nickel or that with niobium. The morphology observed by scanning electron microscopy, gravimetric tests, porosity and adhesion evaluation results indicated that the phosphate

  19. Development of an automated flow injection analysis system for determination of phosphate in nutrient solutions.

    Science.gov (United States)

    Karadağ, Sevinç; Görüşük, Emine M; Çetinkaya, Ebru; Deveci, Seda; Dönmez, Koray B; Uncuoğlu, Emre; Doğu, Mustafa

    2018-01-25

    A fully automated flow injection analysis (FIA) system was developed for determination of phosphate ion in nutrient solutions. This newly developed FIA system is a portable, rapid and sensitive measuring instrument that allows on-line analysis and monitoring of phosphate ion concentration in nutrient solutions. The molybdenum blue method, which is widely used in FIA phosphate analysis, was adapted to the developed FIA system. The method is based on the formation of ammonium Mo(VI) ion by reaction of ammonium molybdate with the phosphate ion present in the medium. The Mo(VI) ion then reacts with ascorbic acid and is reduced to the spectrometrically measurable Mo(V) ion. New software specific for flow analysis was developed in the LabVIEW development environment to control all the components of the FIA system. The important factors affecting the analytical signal were identified as reagent flow rate, injection volume and post-injection flow path length, and they were optimized using Box-Behnken experimental design and response surface methodology. The optimum point for the maximum analytical signal was calculated as 0.50 mL min -1 reagent flow rate, 100 µL sample injection volume and 60 cm post-injection flow path length. The proposed FIA system had a sampling frequency of 100 samples per hour over a linear working range of 3-100 mg L -1 (R 2  = 0.9995). The relative standard deviation (RSD) was 1.09% and the limit of detection (LOD) was 0.34 mg L -1 . Various nutrient solutions from a tomato-growing hydroponic greenhouse were analyzed with the developed FIA system and the results were found to be in good agreement with vanadomolybdate chemical method findings. © 2018 Society of Chemical Industry. © 2018 Society of Chemical Industry.

  20. Efficacy of silver dihydrogen citrate and steam vapor against a human norovirus surrogate, feline calicivirus, in suspension, on glass, and carpet.

    Science.gov (United States)

    Buckley, David; Dharmasena, Muthu; Fraser, Angela; Pettigrew, Charles; Anderson, Jeffery; Jiang, Xiuping

    2018-04-06

    Carpets and other soft surfaces have been associated with prolonged and reoccurring human norovirus (HuNoV) outbreaks. Environmental hygiene programs are important to prevent and control HuNoV outbreaks. Despite our knowledge of HuNoV transmission via soft surfaces, no commercially available disinfectants have been evaluated on carpets. Our aim was to adapt a current standardized method for virucidal testing by assessing two disinfection technologies, silver dihydrogen citrate (SDC) and steam vapor, against one HuNoV surrogate, feline calicivirus (FCV), on wool and nylon carpets. First, we evaluated the effect of both technologies on appearance of carpet. Next, we evaluated the efficacy of SDC in suspension and the efficacy of SDC and steam vapor against FCV on a glass surface, each with and without serum. Lastly, we tested both technologies on two types of carpet, wool and nylon. Both carpets exhibited no obvious color changes; however, SDC treatments left a residue while steam vapor left minor abrasions to fibers. SDC in suspension and on glass reduced FCV by 4.65 and >4.66 log 10 pfu, respectively, but demonstrated reduced efficacy in the presence of serum. However, SDC was only efficacious against FCV on nylon (3.62 log 10 pfu reduction) and not wool (1.82 log 10 pfu reduction). Steam vapor reduced FCV by >4.93 log 10 pfu on glass in 10 sec and >3.68 log 10 pfu reduction on wool and nylon carpet carriers in 90 sec. There was limited reduction to FCV RNA under both treatments compared to infectivity assays but RNA reductions were higher in samples that contained serum. IMPORTANCE Human noroviruses (HuNoV) account for ca. 20% of all diarrheal cases worldwide. Disease symptoms may include diarrhea and vomit with both known to contribute to transmission. Prevention and control of HuNoV are difficult because they are environmentally resilient and resistant to many disinfectants. Several field studies have linked both hard and soft surfaces to HuNoV outbreaks

  1. Chemical treatment of ammonium fluoride solution in uranium reconversion plant

    International Nuclear Information System (INIS)

    Carvalho Frajndlich, E.U. de.

    1992-01-01

    A chemical procedure is described for the treatment of the filtrate, produced from the transformation of uranium hexafluoride (U F 6 ) into ammonium uranyl carbonate (AUC). This filtrate is an intermediate product in the U F 6 to uranium dioxide (U O 2 ) reconversion process. The described procedure recovers uranium as ammonium peroxide fluoro uranate (APOFU) by precipitation with hydrogen peroxide (H 2 O 2 ), and as later step, its calcium fluoride (CaF 2 ) co-precipitation. The recovered uranium is recycled to the AUC production plant. (author)

  2. Thermochemistry of certain rare earth and ammonium double chlorides

    International Nuclear Information System (INIS)

    Usubaliev, D.U.; Abramtsev, V.A.; Kydynov, M.K.; Vilyaev, A.N.

    1987-01-01

    In a calorimeter with isothermal casing at 25 deg C dissolution enthalpies of double chlorides of rare earths and ammonium LnCl 3 x2NH 4 Cl (Ln=La, Sm) and LnCl 3 x3NH 4 Cl (Ln=Gd, Tb, Ho) in water, as well as dissolution enthalpy of rare earth chlorides in solution of ammonium chloride and NH 4 Cl in solution of rare earth chloride, have been measured. Formation enthalpies, standard formation enthalpies, dissociation enthalpies of the above-mentioned double chlorides are calculated

  3. Uranium abundance in some sudanese phosphate ores

    International Nuclear Information System (INIS)

    Adam, A.A.; Eltayeb, M.A.H.

    2009-01-01

    This work was carried out mainly to analysis of some Sudanese phosphate ores, for their uranium abundance and total phosphorus content measured as P 2 O 5 %. For this purpose, 30 samples of two types of phosphate ore from Eastern Nuba Mountains, in Sudan namely, Kurun and Uro areas were examined. In addition, the relationship between uranium and major, and trace elements were obtained, also, the natural radioactivity of the phosphate samples was measured, in order to characterize and differentiate between the two types of phosphate ores. The uranium abundance in Uro phosphate with 20.3% P 2 O 5 is five time higher than in Kurun phosphate with 26.7% P 2 O 5 . The average of uranium content was found to be 56.6 and 310 mg/kg for Kurun and Uro phosphate ore, respectively. The main elements in Kurun and Uro phosphate ore are silicon, aluminum, and phosphorus, while the most abundant trace elements in these two ores are titanium, strontium and barium. Pearson correlation coefficient revealed that uranium in Kurun phosphate shows strong positive correlation with P 2 O 5 , and its distribution is essentially controlled by the variations of P2O5 concentration, whereas uranium in Uro phosphate shows strong positive correlation with strontium, and its distribution is controlled by the variations of Sr concentration. Uranium behaves in different ways in Kurun phosphate and in Uro phosphate. Uro phosphate shows higher concentrations of all the estimated radionuclides than Kurun phosphate. According to the obtained results, it can be concluded that Uro phosphate is consider as secondary uranium source, and is more suitable for uranium recovery, because it has high uranium abundance and low P 2 O 5 %, than Kurun phosphate. (authors) [es

  4. Occurrence and functioning of phosphate solubilizing ...

    African Journals Online (AJOL)

    Occurrence and functioning of phosphate solubilizing microorganisms from oil palm tree ( Elaeis guineensis ) rhizosphere in Cameroon. ... While the use of soluble mineral phosphate fertilizers is the obvious best means to combat phosphate ... in order to improve agricultural production, using low inputs technology. Isolates ...

  5. Grafted wood pulp containing quaternary ammonium group and its application in the removal of different anions from aqueous solution

    International Nuclear Information System (INIS)

    Sokker, H.H.

    2005-01-01

    Network wood pulp based on acrylonitrile has been chemically modified through different reactions to obtain group capable of anion exchange. Graft copolymerization of acrylonitrile onto wood pulp was carried out by using gamma-radiation 60 Co. Factors affecting the grafting process e.g radiation dose and monomer concentration were investigated.The chemical modification of cyano groups were carried out by reaction with ethanol amine producing oxazoline group followed by quaternization of tertiary amine by reaction with benzyl chloride producing quaternary ammonium salt. The grafted and modified wood pulp were characterized by FTIR, SEM and TGA.Qualitative experiments of adsorption were conducted to evaluate the modified wood pulp on fixing sulfate, phosphate,nitrate and dichromate from aqueous solution using batch extractions. Based on the results obtained, it may be concluded that it is possible to modify chemically wood pulp containing cyano groups by different routes for its usage as anion exchanger

  6. Characterization and obtainment of phosphate rock concentrates of Turmequé, Boyacá

    Science.gov (United States)

    Zanguña, S. Quijano; Lozano Gómez, L. F.; Pineda Triana, Y.

    2017-12-01

    The work focuses on the use and exploitation of the mineral concentrates from phosphate rock (PR) coming from mines with a low percentage of phosphorus. The procedure was based on the collection of a source of phosphate rock from the department of Boyacá (municipality of Turmequé), using a randomized design with three replications. The samples were initially milled and sifted using meshes between 140 and 200 US standard, homogenizing them and improving the process of solubility of the phosphorus in the soil. We conduced Z-potential tests, which show that by performing a prior wash on the mineral and maintaining certain concentrations and pH defined, better results are achieved in terms of the buoyancy of the particles in the flotation process. The results obtained from the microflotation tests; both direct and inverse, and the results of chemical composition, with X-Ray Fluorescence (XRF) and X-Ray Diffraction (XRD), before and after the microflotation process, were carried out to obtain of commercial laws grade phosphate rock concentrate, confirm that the protocol used increases by 9% the value of total phosphorus in the collected sample. These concentrates from phosphate rock, could be used in the future for the attainment of simple superphosphate (SSP), with the help of sulphuric acid and ammonium thiosulphate mixtures.

  7. Removal of lead and phosphate ions from aqueous solutions by organo-smectite.

    Science.gov (United States)

    Bajda, Tomasz; Szala, Barbara; Solecka, Urszula

    2015-01-01

    Smectite has been modified using hexadecyltrimethyl ammonium bromide in an amount of double cationic exchange capacity. This alteration makes it possible to use organo-smectite as a sorbent to remove anionic forms. The experiment consisted of the interchangeable sorption of phosphate(V) and lead(II) by organo-smectite. Research was carried out with varying pH (2-5) and various concentrations (0.1-5 mmol/L). Organo-smectite with previously adsorbed lead ions removed more phosphate than the untreated organo-smectite. Experimental data show that lead is more likely to absorb on the organo-smectite than on the organo-smectite with previously adsorbed phosphate ions. It follows that the most effective use of the organo-smectite is through the sorption of first - Pb cations and then PO4 anions. With an increasing concentration of Pb(II) or P(V), the sorption efficiency increases. The maximum sorption efficiency of lead and phosphate ions is observed at pH 5. This enables the removal of harmful lead and phosphorus compounds from waste water and immobilizes them on the sorbent's surface. The alternating reactions of lead and phosphorus ions result in the crystallization of brompyromorphite Pb5(PO4)3Br.

  8. Nitrification and ammonium dynamics in Taihu Lake, China: seasonal competition for ammonium between nitrifiers and cyanobacteria

    Science.gov (United States)

    Hampel, Justyna J.; McCarthy, Mark J.; Gardner, Wayne S.; Zhang, Lu; Xu, Hai; Zhu, Guangwei; Newell, Silvia E.

    2018-02-01

    Taihu Lake is hypereutrophic and experiences seasonal, cyanobacterial harmful algal blooms. These Microcystis blooms produce microcystin, a potent liver toxin, and are linked to anthropogenic nitrogen (N) and phosphorus (P) loads to lakes. Microcystis spp. cannot fix atmospheric N and must compete with ammonia-oxidizing and other organisms for ammonium (NH4+). We measured NH4+ regeneration and potential uptake rates and total nitrification using stable-isotope techniques. Nitrification studies included abundance of the functional gene for NH4+ oxidation, amoA, for ammonia-oxidizing archaea (AOA) and bacteria (AOB). Potential NH4+ uptake rates ranged from 0.02 to 6.80 µmol L-1 h-1 in the light and from 0.05 to 3.33 µmol L-1 h-1 in the dark, and NH4+ regeneration rates ranged from 0.03 to 2.37 µmol L-1 h-1. Nitrification rates exceeded previously reported rates in most freshwater systems. Total nitrification often exceeded 200 nmol L-1 d-1 and was > 1000 nmol L-1 d-1 at one station near a river discharge. AOA amoA gene copies were more abundant than AOB gene copies (p Internal NH4+ regeneration exceeded external N loading to the lake by a factor of 2 but was ultimately fueled by external N loads. Our results thus support the growing literature calling for watershed N loading reductions in concert with existing management of P loads.

  9. Phosphate removal from aqueous solutions using polyaniline/ Ni 0.5 Zn 0.5 Fe 2 O 4 magnetic nanocomposite

    Directory of Open Access Journals (Sweden)

    Mohammad Hossein Tarmahi

    2017-05-01

    Full Text Available Background: Phosphorus is an indispensable element for the growth of animals and plants. There are several environmental problems related to phosphate; therefore, the technical and economic methods of removing phosphate are of great importance. This study evaluated the efficiency of polyaniline/ Ni0.5Zn0.5Fe2O4 magnetic nanocomposite in removing phosphate from aqueous environments. Methods: The adsorbent was characterized by several methods, including X-ray diffraction (XRD, scanning electron microscopy (SEM, vibrating sample magnetometer (VSM, and Fourier transform infrared (FT-IR spectroscopy. Then, the potential of the adsorbentto adsorb phosphate was investigated. The effects of the parameters of contact time (5-60 minutes, pH (3-9, adsorbent dosage (0.05-0.6 g, and initial phosphate concentration (2-100 mg/L on the phosphate removal yield were studied. All phosphate ion concentrations were measured using the ammonium molybdate spectrophotometric method. Results: The results showed that a time of 30 minutes, pH of 5, and adsorbent dose of 0.4 g were the optimum conditions for phosphate removal through adsorption. Increasing the initial concentration of phosphate from 2 to 100 mg/L decreased the removal efficiency from 90.3% to 32%. The experimental data was fitted well with the Freundlich isotherm model (R2 = 0.997. Conclusion: Polyaniline/Ni0.5Zn0.5Fe2O4 magnetic nanocomposite removes phosphate from aqueous solutions with a simple and environmentally benign procedure. The maximum adsorption capacity based on Langmuir isotherm (R2 = 0.931 is 85.4 mg/g. This magnetic nanocomposite is applicable in managing water resource pollution caused by phosphate ions.

  10. Growth and fermentation patterns of Saccharomyces cerevisiae under different ammonium concentrations and its implications in winemaking industry.

    Science.gov (United States)

    Mendes-Ferreira, A; Mendes-Faia, A; Leão, C

    2004-01-01

    To study the effects of assimilable nitrogen concentration on growth profile and on fermentation kinetics of Saccharomyces cerevisiae. Saccharomyces cerevisiae was grown in batch in a defined medium with glucose (200 g l(-1)) as the only carbon and energy source, and nitrogen supplied as ammonium sulphate or phosphate forms under different concentrations. The initial nitrogen concentration in the media had no effect on specific growth rates of the yeast strain PYCC 4072. However, fermentation rate and the time required for completion of the alcoholic fermentation were strongly dependent on nitrogen availability. At the stationary phase, the addition of ammonium was effective in increasing cell population, fermentation rate and ethanol. The yeast strain required a minimum of 267 mg N l(-1) to attain complete dryness of media, within the time considered for the experiments. Lower levels were enough to support growth, although leading to sluggish or stuck fermentation. The findings reported here contribute to elucidate the role of nitrogen on growth and fermentation performance of wine yeast. This information might be useful to the wine industry where excessive addition of nitrogen to prevent sluggish or stuck fermentation might have a negative impact on wine stability and quality. Copyright 2004 The Society for Applied Microbiology

  11. Biogeochemistry of dihydrogen (H2).

    Science.gov (United States)

    Hoehler, Tori M

    2005-01-01

    Hydrogen has had an important and evolving role in Earth's geo- and biogeochemistry, from prebiotic to modern times. On the earliest Earth, abiotic sources of H2 were likely stronger than in the present. Volcanic out-gassing and hydrothermal circulation probably occurred at several times the modern rate, due to presumably higher heat flux. The H2 component of volcanic emissions was likely buffered close to the modern value by an approximately constant mantle oxidation state since 3.9 billion years ago, and may have been higher before that, if the early mantle was more reducing. The predominantly ultramafic character of the early, undifferentiated crust could have led to increased serpentinization and release of H2 by hydrothermal circulation, as in modern ultramafic-hosted vents. At the same time, the reactive atmospheric sink for H2 was likely weaker. Collectively, these factors suggest that steady state levels of H2 in the prebiotic atmosphere were 3-4 orders of magnitude higher than at present, and possibly higher still during transient periods following the delivery of Fe and Ni by large impact events. These elevated levels had direct or indirect impacts on the redox state of the atmosphere, the radiation budget, the production of aerosol hazes, and the genesis of biochemical precursor compounds. The early abiotic cycling of H2 helped to establish the environmental and chemical context for the origins of life on Earth. The potential for H2 to serve as a source of energy and reducing power, and to afford a means of energy storage by the establishment of proton gradients, could have afforded it a highly utilitarian role in the earliest metabolic chemistry. Some origin of life theories suggest the involvement of H2 in the first energy-generating metabolism, and the widespread and deeply-branching nature of H2-utilization in the modern tree of life suggests that it was at least a very early biochemical innovation. The abiotic production of H2 via several mechanisms of water-rock interaction could have supported an early chemosynthetic biosphere. Such processes offer the continued potential for a deep, rock-hosted biosphere on Earth or other bodies in the solar system. The continued evolution of metabolic and community-level versatility among microbes led to an expanded ability to completely exploit the energy available in complex organic matter. Under the anoxic conditions that prevailed on the early Earth, this was accomplished through the linked and sequential action of several metabolic classes of organisms. By transporting electrons between cells, H2 provides a means of linking the activities of these organisms into a highly functional and interactive network. At the same time, H2 concentrations exert a powerful thermodynamic control on many aspects of metabolism and biogeochemical function in these systems. Anaerobic communities based on the consumption of organic matter continue to play an important role in global biogeochemistry even into the present day. As the principal arbiters of chemistry in most aquatic sediments and animal digestive systems, these microbes affect the redox and trace-gas chemistry of our oceans and atmosphere, and constitute the ultimate biological filter on material passing into the rock record. It is in such communities that the significance of H2 in mediating biogeochemical function is most strongly expressed. The advent of phototrophic metabolism added another layer of complexity to microbial communities, and to the role of H2 therein. Anoxygenic and oxygenic phototrophs retained and expanded on the utilization of H2 in metabolic processes. Both groups produce and consume H2 through a variety of mechanisms. In the natural world, phototrophic organisms are often closely juxtaposed with a variety of other metabolic types, through the formation of biofilms and microbial mats. In the few examples studied, phototrophs contribute an often swamping term to the H2 economy of these communities, with important implications for their overall function-including regulation of the redox state of gaseous products, and direct release of large quantities of H2 to the environment. As one of the dominant sources of biological productivity for as much as 2 billion years of Earth's history, these communities have been among the most important agents of long-term global biogeochemical change. On the modern Earth, H2 is present at only trace levels in the atmosphere and oceans. Nonetheless, its function as an arbiter of microbial interactions and chemistry ensures an important role in biogeochemical cycling. The significance of H2 in a global sense may soon increase, as the search for alternative fuels casts attention on the clean-energy potential of hydrogen fuel cells. Already, H2 utilization plays an important role in all three phylogenetic domains of life. Humans may soon add an important new term to this economy. Considerable research is focused on the H2-producing capacities of phototrophic and other microorganisms as potential contributors in this regard. Regardless of source, the large scale utilization of H2 as an energy source could carry important consequences for biogeochemistry.

  12. Sodium benzyl(monoethanol)ammonium bis(gluconatoborate)

    International Nuclear Information System (INIS)

    Tel'zhenskaya, P.N.; Shvarts, E.M.; Vitola, I.M.

    1990-01-01

    Boron compounds with gluconic acid and monoethanol- and benzylamines are synthesized and investigated by physicochemical methods (IR-spectroscopy, thermal decomposition, conductometry, Fischer titration). Tetracoordinated boron has two free hydroxyl groups, dimer of boron-gluconate anion is held by hydrogen bonds, sodium ions and ammonium protonated salts are cations

  13. Rapeseed with tolerance to the non selective herbicide glufosinate ammonium

    Energy Technology Data Exchange (ETDEWEB)

    Rasche, E. [Hoechst Schering AgrEvo GmbH, Frankfurt am Main (Germany)

    1998-12-31

    Weed control with herbicides is essential to grow rapeseed. Glufosinate Ammonium is used as a non selective herbicide successfully in many countries for over 10 years. It conforms well with ever increasing safety standards for human beings, animals and the environment. The tolerance of rapeseed and other crop plants was achieved by genetic modification. A resistance gene (PAT or BAR) was transfered into previously susceptible rapeseed plants. This new approach allowed the development of Glufosinate Ammonium as an almost ideal selective herbicide. In cooperation with major seed companies and by own breeding programmes new Glufosinate tolerant rapeseed varieties and hybrids are developed. Data on metabolism, toxicity, residues, efficacy etc. were generated to get registration for the selective herbicide use. In addition various studies were done for safety assessments of the PAT gene and the modified rapeseed. In spring 1995 Canadian authorities granted worldwide the first approvals for the selective use of Glufosinate Ammonium (trademark Liberty) and Glufosinate tolerant (trademark and logo Liberty Link) spring rapeseed (Canola). After a successful launch in 1995 about 150.000 ha of Liberty Link Canola were grown and treated with Liberty in 1996. The Liberty Link Canola growers were very well satisfied. In a grower survey 84% stated that they will definitely use the Liberty Link System again. In Europe registrations for Glufosinate Ammonium as a selective herbicide and for the first Glufosinate tolerant rapeseed varieties are expected in the course of 1997. The Liberty Link System will be launched in rapeseed most probably in 1998. (orig.)

  14. Monocrystallomimicry in the aerosols of ammonium and cesium halides

    International Nuclear Information System (INIS)

    Melikhov, I.V.; Kitova, E.N.; Kozlovskaya, EhD.; Kamenskaya, A.N.; Mikheev, N.B.; Kulyukhin, S.A.

    1997-01-01

    It is experimentally shown that initial CsI and NH 4 Hal nanocrystals combining into mixed aggregates of polyhedral form (pseudo monocrystals) are formed in the process of cocrystallization of ammonium halide and cesium iodide. The origination and growth of the pseudo monocrystals on the account of successive addition of initial crystals is described by the Fokker-Plank equation [ru

  15. Thermal and chemical analysis of ammonium uranates and intermediate oxides

    International Nuclear Information System (INIS)

    Farah, M.Y.; El-Fekey, S.A.

    1977-01-01

    NH + 4 /U ratio, in ammonium uranate, decreases markedly with lower pH of precipitation, dilution of ammonia used for washing as also rinsing by acetone, methanol, or boiling water and it varies between 0.23 and 0.54. Thermogravimetric plots indicated that variation in percentage loss of weight between 220 deg and 660 deg C was seriously influenced by washing mode. Storing UO 3 under ammonium nitrate solution revealed, that a fraction could have been introduced from aqueous media by cation exchange mechanism. The percentage decreases in weight between 220 deg and 660 deg C. increased from 1.9% for nuclear pure UO 3 , to 3,2% for the trioixde immersed in ammonium nitrate, indicating some uptake of ammonia, amounting to a value of 0.053 to NH + 4 /U. To elucidate the type of binding, the behavior during uranate calcination at various temperatures, durations and depth of calcined layers in tray, was investigated in function of NH + 4 /U ratio. Finally, the study suggested an analytical method for determination of uranium in pure ammonium uranate powders, applicable for both routine and academic works

  16. Profiling the origin of ammonium nitrate: proof-of-principle

    NARCIS (Netherlands)

    Carol-Visser, J.; Farmache, M.A.; Heijden, A.E.D.M. van der

    2011-01-01

    In many Improvised Explosive Devices (IEDs) the main charge consists of ammonium nitrate (AN). For forensic reasons, screening for the origin of AN is of importance. By assessing specifi c characteristics, diff erent AN batches can be profi led, in this way providing extra information which could

  17. Structural characterization of ammonium uranate by infrared spectroscopy

    International Nuclear Information System (INIS)

    Rodriguez S, A.

    1994-01-01

    Infrared spectroscopy have been used to investigate the chemical composition of some ammonium uranates. In this study, I have attempted to establish the interrelationship between the structure of the products, the character of their infrared spectra and x-ray diffraction data capable of consistent interpretation in terms of defining the compounds. (Author)

  18. Nitrate, Nitrite, and Ammonium Variability in Drinking Water Distribution Systems.

    Science.gov (United States)

    Schullehner, Jörg; Stayner, Leslie; Hansen, Birgitte

    2017-03-09

    Accurate assessments of exposure to nitrate in drinking water is a crucial part of epidemiological studies investigating long-term adverse human health effects. However, since drinking water nitrate measurements are usually collected for regulatory purposes, assumptions on (1) the intra-distribution system variability and (2) short-term (seasonal) concentration variability have to be made. We assess concentration variability in the distribution system of nitrate, nitrite, and ammonium, and seasonal variability in all Danish public waterworks from 2007 to 2016. Nitrate concentrations at the exit of the waterworks are highly correlated with nitrate concentrations within the distribution net or at the consumers' taps, while nitrite and ammonium concentrations are generally lower within the net compared with the exit of the waterworks due to nitrification. However, nitrification of nitrite and ammonium in the distribution systems only results in a relatively small increase in nitrate concentrations. No seasonal variation for nitrate, nitrite, or ammonium was observed. We conclude that nitrate measurements taken at the exit of the waterworks are suitable to calculate exposures for all consumers connected to that waterworks and that sampling frequencies in the national monitoring programme are sufficient to describe temporal variations in longitudinal studies.

  19. Ammonium transformation in a nitrogen-rich tidal freshwater marsh

    DEFF Research Database (Denmark)

    Gribsholt, B.; Andersson, M.; Boschker, H.T.S.

    2006-01-01

    The fate and transport of watershed-derived ammonium in a tidal freshwater marsh fringing the nutrient rich Scheldt River, Belgium, was quantified in a whole ecosystem 15N labeling experiment. In late summer (September) we added 15N-NH4+ to the flood water entering a 3477 m2 tidal freshwater marsh...

  20. Growth features of ammonium hydrogen d-tartrate single crystals

    Indian Academy of Sciences (India)

    Unknown

    Abstract. Ammonium hydrogen d-tartrate (d-AHT) single crystals were grown in silica gel. The growth fea- ... solution (specific gravity, 1⋅04 g/cc) with d-tartaric acid solution having ... resulting in the production of crystal nuclei. The interface.

  1. Ammonium dinitramide (ADN)-Prilling, coating, and characterization

    Energy Technology Data Exchange (ETDEWEB)

    Heintz, Thomas; Pontius, Heike; Aniol, Jasmin; Birke, Christoph; Leisinger, Karlfred; Reinhard, Werner [Fraunhofer-Institut Chemische Technologie ICT, Pfinztal (Germany)

    2009-06-15

    Ammonium dinitramide (ADN) is the promising oxidizer, which is expected to be applied, e.g., in solid rocket propellants. The manufacturing of spherical ADN particles (the so-called ADN-Prills) with useful morphology and reproducible quality is realized by means of the emulsion crystallization process. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  2. Anaerobic ammonium oxidation by Anammox bacteria in the Black Sea

    NARCIS (Netherlands)

    Sinninghe Damsté, J.S.; Kuypers, M.M.M.; Sliekers, O.; Lavik, G.; Schmid, M.; Jørgensen, B.B.; Kuenen, J.G.; Strous, M.; Jetten, M.S.M.

    2003-01-01

    The availability of fixed inorganic nitrogen (nitrate, nitrite and ammonium) limits primary productivity in many oceanic regions1. The conversion of nitrate to N2 by heterotrophic bacteria (denitrification) is believed to be the only important sink for fixed inorganic nitrogen in the ocean2. Here we

  3. Cultivation, detection, and ecophysiology of anaerobic ammonium-oxidizing bacteria.

    Science.gov (United States)

    Kartal, Boran; Geerts, Wim; Jetten, Mike S M

    2011-01-01

    Anaerobic ammonium-oxidizing (anammox) bacteria oxidize ammonium with nitrite under anoxic conditions. The anammox process is currently used to remove ammonium from wastewater and contributes significantly to the loss of fixed nitrogen from the oceans. In this chapter, we focus on the ecophysiology of anammox bacteria and describe new methodologies to grow these microorganisms. Now, it is possible to enrich anammox bacteria up to 95% with a membrane bioreactor that removes forces of selection for fast settling aggregates and facilitates the growth of planktonic cells. The biomass from this system has a high anaerobic ammonium oxidation rate (50 fmol NH(4)(+) · cell(-1) day(-1)) and is suitable for many ecophysiological and molecular experiments. A high throughput Percoll density gradient centrifugation protocol may be applied on this biomass for further enrichment (>99.5%) of anammox bacteria. Furthermore, we provide an up-to-date list of commonly used primers and introduce protocols for quantification and detection of functional genes of anammox bacteria in their natural environment. Copyright © 2011 Elsevier Inc. All rights reserved.

  4. Cell biology of anaerobic ammonium-oxidizing bacteria

    NARCIS (Netherlands)

    Niftrik, L.A.M.P. van

    2008-01-01

    Anammox bacteria perform anaerobic ammonium oxidation to dinitrogen gas and belong to the phylum Planctomycetes. Whereas most Prokaryotes consist of one compartment, the cytoplasm bounded by the cytoplasmic membrane and cell wall, the species within this phylum are compartmentalized by intracellular

  5. Surge ammonium uptake in macroalgae from a coral atoll

    Digital Repository Service at National Institute of Oceanography (India)

    Raikar, V.; Wafar, M.V.M.

    of Phycology 36, 680?685. Crossland, C.J., Hatcher, B.G., Smith, S.V., 1991. Role of coral reefs in global ocean production. Coral Reefs 10, 55-64. Danilo, Dy. T., Yap, H.T., 2001. Surge ammonium uptake of the cultured seaweed, Kappaphycus alvarezii (Doty...

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

    Science.gov (United States)

    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.

  7. Ammonia loss, ammonium and nitrate accumulation from mixing ...

    African Journals Online (AJOL)

    Ammonia loss from urea significantly hinders efficient use of urea in agriculture. In order to reduce ammonia loss and, at the same time, improve beneficial accumulation of soil exchangeable ammonium and nitrate for efficient utilization by plants, this laboratory study was conducted to determine the effect of mixing urea with ...

  8. Effect of nitrogen concentration of urea ammonium nitrate, and ...

    African Journals Online (AJOL)

    Liquid urea ammonium nitrate (UAN) was applied to dryland Pennisetum clandestinum (Kikuyu (Chiov)) and Cynodon hybrid (Coastcross II (L.) (Pers.)) pastures at two levels (207 and 414 kg N/ha/season) and at three concentrations (10, 5; 21 and 42% N) of nitrogen. The degree of leaf scorch increased as both the amount ...

  9. Nitrate and ammonium levels of some water bodies and their ...

    African Journals Online (AJOL)

    The present study examined the nitrate (NO3-) and ammonium (NH4+) levels of Rivers Wouri and Dibamba and some streams that feed them. The interaction of NO3- and NH4+ with some soil properties was also investigated. It was necessitated by the usage of these rivers for livelihood, despite the deposition of discharges ...

  10. Acid mine water neutralisation with ammonium hydroxide and ...

    African Journals Online (AJOL)

    This study showed that NH4OH can be used for treatment of acid mine drainage rich in sulphates and NH4OH can be recycled in the process. Hydrated lime treatment resulted in removal of the remaining ammonia using a rotary evaporator. Keywords: acid mine water, ammonium hydroxide, barium hydroxide, sulphate ...

  11. Zirconium Phosphate Supported MOF Nanoplatelets.

    Science.gov (United States)

    Kan, Yuwei; Clearfield, Abraham

    2016-06-06

    We report a rare example of the preparation of HKUST-1 metal-organic framework nanoplatelets through a step-by-step seeding procedure. Sodium ion exchanged zirconium phosphate, NaZrP, nanoplatelets were judiciously selected as support for layer-by-layer (LBL) assembly of Cu(II) and benzene-1,3,5-tricarboxylic acid (H3BTC) linkers. The first layer of Cu(II) is attached to the surface of zirconium phosphate through covalent interaction. The successive LBL growth of HKUST-1 film is then realized by soaking the NaZrP nanoplatelets in ethanolic solutions of cupric acetate and H3BTC, respectively. The amount of assembled HKUST-1 can be readily controlled by varying the number of growth cycles, which was characterized by powder X-ray diffraction and gas adsorption analyses. The successful construction of HKUST-1 on NaZrP was also supported by its catalytic performance for the oxidation of cyclohexene.

  12. Electrochemical oxidation of quaternary ammonium electrolytes : Unexpected side reactions in organic electrochemistry

    NARCIS (Netherlands)

    Nouri Nigjeh, Eslam; de Vries, Marcel; Bruins, Andries P.; Bischoff, Rainer; Permentier, Hjalmar P.

    Quaternary ammonium salts are among the most widely used electrolytes in organic electrochemistry, but there is little known about their unwanted side oxidation reactions. We have, therefore, studied the constant potential oxidation products of quaternary ammonium electrolytes using mass

  13. Phosphate-a poison for humans?

    Science.gov (United States)

    Komaba, Hirotaka; Fukagawa, Masafumi

    2016-10-01

    Maintenance of phosphate balance is essential for life, and mammals have developed a sophisticated system to regulate phosphate homeostasis over the course of evolution. However, due to the dependence of phosphate elimination on the kidney, humans with decreased kidney function are likely to be in a positive phosphate balance. Phosphate excess has been well recognized as a critical factor in the pathogenesis of mineral and bone disorders associated with chronic kidney disease, but recent investigations have also uncovered toxic effects of phosphate on the cardiovascular system and the aging process. Compelling evidence also suggests that increased fibroblastic growth factor 23 and parathyroid hormone levels in response to a positive phosphate balance contribute to adverse clinical outcomes. These insights support the current practice of managing serum phosphate in patients with advanced chronic kidney disease, although definitive evidence of these effects is lacking. Given the potential toxicity of excess phosphate, the general population may also be viewed as a target for phosphate management. However, the widespread implementation of dietary phosphate intervention in the general population may not be warranted due to the limited impact of increased phosphate intake on mineral metabolism and clinical outcomes. Nonetheless, the increasing incidence of kidney disease or injury in our aging society emphasizes the potential importance of this issue. Further work is needed to more completely characterize phosphate toxicity and to establish the optimal therapeutic strategy for managing phosphate in patients with chronic kidney disease and in the general population. Copyright © 2016 International Society of Nephrology. Published by Elsevier Inc. All rights reserved.

  14. Investigation of electric discharge treatment of water for ammonium nitrogen removal

    International Nuclear Information System (INIS)

    Nazarenko, O.B.; Shubin, B.G.

    2007-01-01

    The possibility of water purification from ammonium nitrogen using pulsed electric discharge in water-air mixtures was investigated. The model solution of chlorous ammonium was used in experiments. The concentration of ions ammonium was about 300 mg/l. Achieved reduction of ammonium concentration was about 35%. In this paper the mechanism of this process is discussed. The ways to increasing efficiency of this method are proposed

  15. Preparation of wheat straw based superabsorbent resins and their applications as adsorbents for ammonium and phosphate removal.

    Science.gov (United States)

    Liu, Jia; Su, Yuan; Li, Qian; Yue, Qinyan; Gao, Baoyu

    2013-09-01

    A novel wheat straw cellulose-g-poly (potassium acrylate)/polyvinyl alcohol (WSC-g-PKA/PVA) semi-interpenetrating polymer networks (semi-IPNs) superabsorbent resin (SAR) was prepared by graft copolymerization. The structure and performance of the WSC-g-PKA/PVA semi-IPNs SAR was studied and compared with those of wheat straw cellulose-g-poly (potassium acrylate) (WSC-g-PKA) SAR. The effects of various experimental parameters such as solution pH, concentration, contact time and ion strength on NH4(+) and PO4(3-) removal from solutions were investigated. Equilibrium isotherm data of adsorption of both NH4(+) and PO4(3-) were well fitted to the Freundlich model. Kinetic analysis showed that the pseudo-second-order kinetic model was more suitable for describing the whole adsorption process of NH4(+) and PO4(3-) on SARs. Overall, WSC-g-PKA/PVA semi-IPNs SAR showed better properties in comparison with WSC-g-PKA SAR and it could be considered as one efficient material for the removal and recovery of nitrogen and phosphorus with the agronomic reuse as a fertilizer. Copyright © 2013 Elsevier Ltd. All rights reserved.

  16. Applications of isotope techniques for the assessment of soil phosphorus status and evaluation of rock phosphates as phosphorus sources for plants in subtropical China

    International Nuclear Information System (INIS)

    Xiong, L.M.; Zhou, Z.G.; Feng, G.L.; Lu, R.K.; Fardeau, J.C.

    2002-01-01

    In an attempt to assess current soil phosphorus status and evaluate the effectiveness of local rock phosphates in subtropical China, nearly 40 representative soil samples from this region were collected and characterized by using 32 P isotope and chemical extraction techniques. Pot experiments, incubation studies and field trials were conducted to investigate the interaction of rock phosphates and water-soluble phosphates as well as the effects of rock phosphate on soil chemical properties in selected soils. Results indicated that these soils were generally low in available phosphorus and high in P-fixing capacity. The soil characteristics dictated that the employed isotope kinetic model was less successful in predicting plant P uptake than the chemical procedures tested. A new chemical extraction method consisting of sodium bicarbonate and ammonium fluoride was proposed to evaluate available P in these Solis. Data on available P generated with the proposed method gave the best prediction of plant uptake amongst all methods compared. In a pot experiment, the combined application of soluble P fertilizer with local rock phosphate significantly enhanced plant growth and increased P uptake. This positive interaction was attributed to the improved soil chemical properties due to the application of low-grade rock phosphates, as demonstrated in incubation studies. These results suggest that rock phosphate-based fertilizers should be good alternative fertilizers for plants in similar acidic soils in southern China. (author)

  17. Influence of Ammonium Salt and Fermentation pH on Acarbose ...

    African Journals Online (AJOL)

    Purpose: To investigate the effect of ammonium salts and fermentation pH on the biosynthesis of acarbose by Streptomyces M37. Methods: Different ammonium salts were added to the fermentation broth of Streptomyces M37 to explore their effects on acarbose production. The concentration and addition time of ammonium ...

  18. 78 FR 35258 - Solid Agricultural Grade Ammonium Nitrate from Ukraine: Continuation of Antidumping Duty Order

    Science.gov (United States)

    2013-06-12

    ... agricultural grade ammonium nitrate from Ukraine would likely lead to continuation or recurrence of dumping... the Order on solid agricultural grade ammonium nitrate from Ukraine would be likely to lead to... Ammonium Nitrate from Ukraine: Continuation of Antidumping Duty Order AGENCY: Import Administration...

  19. 76 FR 39847 - Solid Fertilizer Grade Ammonium Nitrate From the Russian Federation; Final Results of the...

    Science.gov (United States)

    2011-07-07

    ... duty order on ammonium nitrate from Russia would be likely to lead to continuation or recurrence of... Ammonium Nitrate From the Russian Federation; Final Results of the Expedited Sunset Review of Antidumping... review of the suspended antidumping duty investigation on solid fertilizer grade ammonium nitrate...

  20. 76 FR 49449 - Continuation of Antidumping Duty Order on Solid Fertilizer Grade Ammonium Nitrate From the...

    Science.gov (United States)

    2011-08-10

    ... nitrate (``ammonium nitrate'') from the Russian Federation (``Russia'') would likely lead to continuation... Duty Order on Solid Fertilizer Grade Ammonium Nitrate From the Russian Federation AGENCY: Import... ammonium nitrate suspended investigation. See Initiation of Five-Year (``Sunset'') Review, 76 FR 11202...

  1. Different rates of synthesis and degradation of two chloroplastic ammonium-inducible NADP-specific glutamate dehydrogenase isoenzymes during induction and deinduction in Chlorella sorokiniana cells

    International Nuclear Information System (INIS)

    Bascomb, N.F.; Prunkard, D.E.; Schmidt, R.R.

    1987-01-01

    The kinetics of accumulation (per milliliter of culture) of the α- and β-subunits, associated with chloroplast-localized ammonium inducible nicotinamide adenine dinucleotide phosphate-specific glutamate dehydrogenase (NADP-GDH) isoenzymes, were measured during a 3 hour induction of synchronized daughter cells of Chlorella sorokiniana in 29 millimolar ammonium medium under photoautotrophic conditions. The β-subunit holoenzyme(s) accumulated in a linear manner for 3 hours without an apparent induction lag. A 40 minute induction lag preceded the accumulation of the α-subunit holoenzyme(s). After 120 minutes, the α-subunit ceased accumulating and thereafter remained at a constant level. From pulse-chase experiments, using 35 SO 4 and immunochemical procedures, the rate of synthesis of the α-subunit was shown to be greater than the β-subunit during the first 80 minutes of induction. The α- and β-subunits had different rates of degradation during the induction period (t/sub 1/2/ = 50 versus 150 minutes, respectively) and during the deinduction period (t/sub 1/2/ = 5 versus 13.5 minutes) after removal of ammonium from the culture. During deinduction, total NADP-GDH activity decreased with a half-time of 9 minutes. Cycloheximide completely inhibited the synthesis and degradation of both subunits. A model for regulation of expression of the NADP-GDH gene was proposed

  2. Sources et marché du sulfate d'ammonium Sources of and Market for Ammonium Sulfate

    Directory of Open Access Journals (Sweden)

    Loussouarn C.

    2006-11-01

    Full Text Available Engrais azoté le plus utilisé dans le monde jusqu'en 1970, le sulfate d'ammonium ne représente plus aujourd'hui que 4 % de la fertilisation azotée. Avec une teneur en azote de 21 % seulement, il a été peu à peu remplacé comme engrais universel par des produits plus concentrés, notamment l'urée et le nitrate d'ammonium. Obtenu pour plus de 40 % comme sous-produit dans la synthèse de monomères comme le caprolactame, l'acrylonitrile ou le méthacrylate de méthyle, et pour près de 10 % dans le traitement des gaz de cokerie, sa production dépend largement des développements du marché des fibres synthétiques, et, dans une moindre mesure, de la sidérurgie et de la métallurgie. Dans les pays développés, où la production est essentiellement fatale, le volume du marché est et sera plus fonction de la disponibilité du sulfate d'ammonium que de la demande ou de facteurs de marché; sa consommation ne résidera plus que dans des applications spécifiques pour lesquelles il sera bien adapté. Par contre, l'intérêt croissant pour compenser le déficit en soufre de certains sols, et les qualités agronomiques propres du sulfate d'ammonium laissent entrevoir la possibilité d'un essor de son utilisation dans certaines régions en voie de développernent. Ammonium sulfate was the most worldwide nitrogenous fertilizer used up to 1970. Today, it makes up only 4% of nitrogenous fertilization. With a nitrogen content of only 21%, it has gradually been replaced as a universal fertilizer by more concentrated products, particularly urea and ammonium nitrate. More than 40% of the ammonium sulfate is obtained as a by-product from the synthesis of monomers such as caprolactam, acrylonitrile or methyl methacrylate, and nearly 10% from coking gas processing. Its production depends extensively on the development of the market for synthetic fibers and, to a lesser extent, on the steel and metallurgical industries. In the industrialized countries

  3. Phosphate vibrations as reporters of DNA hydration

    Science.gov (United States)

    Corcelli, Steven

    The asymmetric phosphate stretch vibrational frequency is extraordinarily sensitive to its local solvent environment. Using density functional theory calculations on the model compound dimethyl phosphate, the asymmetric phosphate stretch vibrational frequency was found to shift linearly with the magnitude of an electric field along the symmetry axis of the PO2 moiety (i.e. the asymmetric phosphate stretch is an excellent linear vibrational Stark effect probe). With this linear relationship established, asymmetric phosphate stretch vibrational frequencies were computed during the course of a molecular dynamics simulation of fully hydrated DNA. Moreover, contributions to shifts in the frequencies from subpopulations of water molecules (e.g. backbone, minor groove, major groove, etc.) were calculated to reveal how phosphate vibrations report the onset of DNA hydration in experiments that vary the relative humidity of non-condensing (dry) DNA samples.

  4. Application of Calcium Phosphate Materials in Dentistry

    Directory of Open Access Journals (Sweden)

    Jabr S. Al-Sanabani

    2013-01-01

    Full Text Available Calcium phosphate materials are similar to bone in composition and in having bioactive and osteoconductive properties. Calcium phosphate materials in different forms, as cements, composites, and coatings, are used in many medical and dental applications. This paper reviews the applications of these materials in dentistry. It presents a brief history, dental applications, and methods for improving their mechanical properties. Notable research is highlighted regarding (1 application of calcium phosphate into various fields in dentistry; (2 improving mechanical properties of calcium phosphate; (3 biomimetic process and functionally graded materials. This paper deals with most common types of the calcium phosphate materials such as hydroxyapatite and tricalcium phosphate which are currently used in dental and medical fields.

  5. Preparation of nanodispersed titania using stabilized ammonium nitrate melts

    KAUST Repository

    Raciulete, Monica

    2010-10-01

    An expedite one-step approach using simple precursors has been proposed to obtain metallic oxide compounds and exemplified by preparation of highly dispersed TiO2. The technique consists in heating to 400500 °C of molten ammonium nitrate stabilized with an organic nitrogen-containing compound (urea, melamine, ammonium oxalate) and containing dissolved metal salt precursor (TiOCl2). The crystallites of the resulting TiO2 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. © 2010 Elsevier Inc. All rights reserved.

  6. Thermal decomposition of ammonium uranate; X-ray study

    International Nuclear Information System (INIS)

    El-Fekey, S.A.; Rofail, N.H.; Khilla, M.A.

    1984-01-01

    Ammonium uranate was precipitated from a nuclear-pure uranyl nitrate solution using gaseous ammonia. Thermal decomposition of the obtained uranate, at different calcining temperatures, resulted in the formation of amorphous (A-)UO 3 , β-UO 3 , UOsub(2.9), U 3 O 8 (H) and U 3 O 8 (O). The influence of ammonia content, occluded nitrate ions and rate of heating, on the formation of these phases, was studied using X-ray powder diffraction analysis. The results indicated that ammonium uranate UO 2 (OH)sub(2-x)(ONH 4 )x . YH 2 O is a continuous non-stoichiometric system is a continuous non-stoichiometric system with no intermediate stoichiometric compounds and its composition varies according to mode of preparation. The results indicated also that the rate of heating and formation of hydrates are important factors for both UOsub(2.9) and U 3 O 8 (O) formation. (orig.)

  7. Pilot scale for preparation of ammonium uranyl carbonate

    International Nuclear Information System (INIS)

    Santos, L.R. dos.

    1989-01-01

    The procedure adopted for obtaining Ammonium Uranyl Carbonate (AUC) from uranium hexafluoride (UF sub(6)) or aqueous solutions of uranylnitrate (UO sub(2)(NO sub(3)) sub(2)) is described in the present work. This procedure involves the precipitation of AUC in a chemical reactor by the addition of gaseous UF sub(6) or solutions of uranylnitrate to NH sub(3) and CO sub(2) gases in a solution containing ammonium bicarbonate, where pH and temperature are controlled. Details regarding the characterization and quality control methods in the preparation of AUC are presented along with their physical and chemical properties. Some informations about effluents generated during the process are presented too. An attempt is made to correlate the parameters involved in the precipitation process of AUC and their characteristics. (author)

  8. Volumetric properties of ammonium nitrate in N,N-dimethylformamide

    International Nuclear Information System (INIS)

    Vranes, Milan; Dozic, Sanja; Djeric, Vesna; Gadzuric, Slobodan

    2012-01-01

    Highlights: ► We observed interactions and changes in the solution using volumetric properties. ► The greatest influence on the solvent–solvent interactions has temperature. ► The smallest influence temperature has on the ion–ion interactions. ► Temperature has no influence on concentrated systems and partially solvated melts. - Abstract: The densities of the ammonium nitrate in N,N-dimethylformamide (DMF) mixtures were measured at T = (308.15 to 348.15) K for different ammonium nitrate molalities in the range from (0 to 6.8404) mol·kg −1 . From the obtained density data, volumetric properties (apparent molar volumes and partial molar volumes) have been evaluated and discussed in the term of respective ionic and dipole interactions. From the apparent molar volume, determined at various temperatures, the apparent molar expansibility and the coefficients of thermal expansion were also calculated.

  9. Evaluation of oral abdominal contrast agent containing ferric ammonium citrate

    International Nuclear Information System (INIS)

    Shiga, Toshiko; Kawamura, Yasutaka; Iwasaki, Toshiko

    1991-01-01

    We evaluated the effectiveness of oral MRI contrast agent containing ferric ammonium citrate. Twenty patients were arbitrarily divided into 2 groups according to the given dose of 100 and 200 mg Fe of oral MRI contrast agent. MRI was performed before and immediately after ingesting 300 ml solution of oral MRI contrast agent using a 1.5 T superconducting system (GE: Signa). Each dose of 100 and 200 mg Fe of oral MRI contrast agent produced sufficient enhancement of gastrointestinal tract, enough to make clear the pancreatic contour and porta hepatis. There was no significant change in blood and urine analysis observed after taking oral MRI contrast agent. The use of ferric ammonium citrate as an oral MRI contrast agent seems to add valuable information in performing upper abdominal MRI imaging. (author)

  10. Exciplex emission from amphiphilic polysilanes bearing ammonium moieties

    International Nuclear Information System (INIS)

    Yamaki, T.; Nakashiba, Y.; Asai, K.; Ishigure, K.; Shibata, H.

    1997-01-01

    We were the first to observe two emission bands in the visible region for some kinds of ammonium-type amphiphilic polysilanes both in solutions and in thin films. One, a broad emission band at 400-500 nm not due to a σ * →σ transition, was observed only for methylphenylsilane-based polymer solutions. The appearance of this low-energy emission is reasonably explained by considering the intramolecular exciplex formation between a Si-conjugated main chain and an ammonium site in the same monomer unit. The other, an emission band at the longer wavelength (around 560 nm), was found in the solvent-cast films where each molecule is randomly located, in addition to that observed for the solutions. This emission, which was not observed for the oriented LB films, is considered to originate from an intermolecular interaction. (orig.)

  11. Crystalline cerium(IV) phosphates

    International Nuclear Information System (INIS)

    Herman, R.G.; Clearfield, A.

    1976-01-01

    The ion exchange behaviour of seven crystalline cerium(IV) phosphates towards some of the alkali metal cations is described. Only two of the compounds (A and C) possess ion exchange properties in acidic solutions. Four others show some ion exchange characteristics in basic media with some of the alkali cations. Compound G does not behave as an ion exchanger in solutions of pH + , but show very little Na + uptake. Compound E undergoes ion exchange with Na + and Cs + , but not with Li+. Both Li + and Na + are sorbed by compounds A and C. The results are indicative of structures which show steric exclusion phenomena. (author)

  12. SENSITIVITY OF MORNINGGLORY PLANTS AND THEIR PROGENIES TO GLUFOSINATE AMMONIUM

    OpenAIRE

    BRITO, I.P.F.S.; MORAES, C.P.; MARCHESI, B.B.; CARBONARI, C.A.; VELINI, E.D.

    2017-01-01

    ABSTRACT The sensitivity of weed species to herbicides is variable, and the behavior can be repeated or not in the next generation. The objective of this study was to evaluate the response of morningglory plants to different doses of glufosinate ammonium and the sensitivity of plant populations and their progenies to the herbicide. Three studies were conducted, all in a greenhouse and repeated in two periods. In the first study, two experiments were conducted to examine the dose-response curv...

  13. Investigation of ammonium trinitratouranylate complexing with diethyl ether

    International Nuclear Information System (INIS)

    Khod'ko, N.N.; Kolevich, T.A.; Umrejko, D.S.

    1989-01-01

    Interaction of ammonium trinitratouranylate (ATNU) with diethyl ether is investigated. It is shown, that adduct of UO 2 (NO 3 ) 2 · 2(C 2 H 5 ) 2 O coposition is formed in the indicated solvent due to incongruent solubility of ANTU. Analogous compound is obtained at ether effect on uranyl anhydrous nitrate. The matter is determined and investigated by means of chemical, thermal analyses and oscillating spectroscopy

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

    Science.gov (United States)

    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.

  15. Proton- and ammonium- sensing by histaminergic neurons controlling wakefulness.

    Directory of Open Access Journals (Sweden)

    Yvgenij eYanovsky

    2012-04-01

    Full Text Available Orexinergic and histaminergic neurons in the posterior hypothalamus are involved in the control of arousal. Extracellular levels of acid /CO2 are fundamental physicochemical signals controlling wakefulness and breathing. Acidification excites orexinergic neurons like the chemosensory neurons in the brain stem. Hypercapnia induces c-Fos expression, a marker for increased neuronal activity, in the rat histaminergic tuberomamillary nucleus (TMN, but the mechanisms of this excitation are unknown. Acid-sensing ion channels (ASICs are gated by protons and also by ammonium. Recordings in rat brain slices revealed now that acidification within the physiological range (pH from 7.3 to 7.0 as well as ammonium chloride (5mM excite histaminergic neurons. We detected variable combinations of 4 known types of ASICs in single TMN neurons, along with the pharmacological properties of pH-induced current. At pH 7.0 however, activation of ASICs in TMN neurons was negligible. Block of type I metabotropic glutamate receptors abolished proton- but not ammonium- induced excitation. Mouse TMN neurons were identified within a novel HDC-Cre transgenic reporter mouse line. In contrast to the rat these lacked pH 7.0-induced excitation and showed only a minimal response to the mGluR I agonist DHPG (0.5µM. Ammonium-induced excitation was similar in mouse and rat. Thus glutamate, which is released by glial cells and orexinergic axons amplifies CO2/acid-induced arousal through the recruitment of the histaminergic system in rat but not in mouse. These results are relevant for the understanding of neuronal mechanisms controlling H+/CO2-induced arousal in hepatic encephalopathy and obstructive sleep apnoea. The new HDC-Cre mouse model will be a useful tool for studying the physiological and pathophysiological roles of the histaminergic system.

  16. ITP determination of potassium and ammonium in fertilizers and silage

    Czech Academy of Sciences Publication Activity Database

    Nováková, Michaela; Křivánková, Ludmila; Skalická, I.; Bartoš, M.; Vytřas, K.

    2008-01-01

    Roč. 67, Suppl. (2008), S63-S68 ISSN 0009-5893. [Advances in Chromatography and Electrophoresis 2007 and Chiranal 2007. Olomouc, 24.06.2007-27.06.2007] R&D Projects: GA ČR GA203/05/2106; GA AV ČR IAA400310703 Institutional research plan: CEZ:AV0Z40310501 Keywords : capillary electrophoresis * ammonium * potassium Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 1.312, year: 2008

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

    Science.gov (United States)

    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.

  18. Development of antibacterial quaternary ammonium silane coatings on polyurethane catheters

    Czech Academy of Sciences Publication Activity Database

    Zanini, S.; Polissi, A.; Maccagni, E.A.; Dell'Orto, E.C.; Liberatore, Chiara; Riccardi, C.

    2015-01-01

    Roč. 451, Aug (2015), 78-84 ISSN 0021-9797 R&D Projects: GA MŠk EE2.3.20.0143 Grant - others:OP VK 6(XE) CZ.1.07/2.3.00/20.0143 Institutional support: RVO:68378271 Keywords : plasma-induced graft-polymerization * acrylic acid * ATR/FTIR * AFM * quaternary ammonium silane * Escherichia coli Subject RIV: BH - Optics, Masers, Lasers Impact factor: 3.782, year: 2015

  19. Contribution of Drinking Water Softeners to Daily Phosphate Intake in Slovenia

    Directory of Open Access Journals (Sweden)

    Gregor Jereb

    2017-10-01

    Full Text Available The cumulative phosphate intake in a typical daily diet is high and, according to several studies, already exceeds recommended values. The exposure of the general population to phosphorus via drinking water is generally not known. One of the hidden sources of phosphorus in a daily diet is sodium polyphosphate, commonly used as a drinking water softener. In Slovenia, softening of drinking water is carried out exclusively within the internal (household drinking water supply systems to prevent the accumulation of limescale. The aim of the study was to determine the prevalence of sodium phosphates in the drinking water in Slovenia in different types of buildings, to determine residents’ awareness of the presence of chemical softeners in their drinking water, and to provide an exposure assessment on the phosphorus intake from drinking water. In the current study, the presence of phosphates in the samples of drinking water was determined using a spectrophotometric method with ammonium molybdate. In nearly half of the samples, the presence of phosphates as water softeners was confirmed. The measured concentrations varied substantially from 0.2 mg PO4/L to 24.6 mg PO4/L. Nearly 70% of the respondents were not familiar with the exact data on water softening in their buildings. It follows that concentrations of added phosphates should be controlled and the consumers should be informed of the added chemicals in their drinking water. The health risks of using sodium polyphosphate as a drinking water softener have not been sufficiently investigated and assessed. It is highly recommended that proper guidelines and regulations are developed and introduced to protect human health from adverse effects of chemicals in water intended for human consumption.

  20. Contribution of Drinking Water Softeners to Daily Phosphate Intake in Slovenia.

    Science.gov (United States)

    Jereb, Gregor; Poljšak, Borut; Eržen, Ivan

    2017-10-06

    The cumulative phosphate intake in a typical daily diet is high and, according to several studies, already exceeds recommended values. The exposure of the general population to phosphorus via drinking water is generally not known. One of the hidden sources of phosphorus in a daily diet is sodium polyphosphate, commonly used as a drinking water softener. In Slovenia, softening of drinking water is carried out exclusively within the internal (household) drinking water supply systems to prevent the accumulation of limescale. The aim of the study was to determine the prevalence of sodium phosphates in the drinking water in Slovenia in different types of buildings, to determine residents' awareness of the presence of chemical softeners in their drinking water, and to provide an exposure assessment on the phosphorus intake from drinking water. In the current study, the presence of phosphates in the samples of drinking water was determined using a spectrophotometric method with ammonium molybdate. In nearly half of the samples, the presence of phosphates as water softeners was confirmed. The measured concentrations varied substantially from 0.2 mg PO4/L to 24.6 mg PO4/L. Nearly 70% of the respondents were not familiar with the exact data on water softening in their buildings. It follows that concentrations of added phosphates should be controlled and the consumers should be informed of the added chemicals in their drinking water. The health risks of using sodium polyphosphate as a drinking water softener have not been sufficiently investigated and assessed. It is highly recommended that proper guidelines and regulations are developed and introduced to protect human health from adverse effects of chemicals in water intended for human consumption.

  1. Radiological impact of use of phosphate fertilizers

    International Nuclear Information System (INIS)

    Shukla, V.K.; Chinnaesakki, S.; Sartandel, S.J.; Shanbhag, A.A.; Puranik, V.D.

    2003-01-01

    The paper describes the results of gamma spectrometric measurements of 238 U, 233 Th, 226 Ra and 40 K in rock phosphates and various types of phosphate fertilizers and by-products. The increase in soil natural radioactivity has been assessed for major Indian crops. No significant increase in soil natural radioactivity is expected due to the application of phosphate fertilizers for agricultural productions. (author)

  2. Uranium and heavy metals in phosphate fertilizers

    International Nuclear Information System (INIS)

    Khater, Ashraf E.M.; King Saud University, Riyadh

    2008-01-01

    Full text: Agricultural applications of chemical fertilizers are a worldwide practice. The specific activity of uranium-238 and heavy metals in phosphate fertilizers depends on the phosphate ore from which the fertilizer produced and on the chemical processing of the ore. Composite phosphate fertilizers samples were collected and the uranium-238 specific activity, in Bq/kg, and As, Cd, Cu, Pb, Se concentration were measured. The annual addition of these elements in soil due to soil fertilization were calculated and discussed. (author)

  3. Ammonium uptake by phytoplankton regulates nitrification in the sunlit ocean.

    Science.gov (United States)

    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 (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.

  4. Study of stripping cristallization processus of AUC with ammonium carbonate

    International Nuclear Information System (INIS)

    Chegrouche, Salah.

    1987-09-01

    This study is concerned with direct crystallization of ammonium uranyl carbonate (AUC) from a uranium loaded organic phase (30% TBP in kerosene), with ammonium carbonate (NH 4 ) 2 CO 3 . The effects of operating conditions ((NH 4 ) 2 CO 3 concentration, flow-ratio, residence time, temperature) on the physical properties of AUC crystals (particle size distribution, specific surface, density...) are reported. All products were identified (both by chemical analysis, X-Ray diffraction) as being ammonium uranyl carbonate crystals (AUC). The results show that a high phase ratio and (NH 4 ) 2 CO 3 concentration favor the formation of fine AUC grains and aggregates. This is due mainly to the high concentration of NH + 4 in the system which leads to a high solution supersaturation and consequently to a rapid formation rate of crystal (germination). The reverse phenomenon is observed at low phase ratio and (NH 4 ) 2 CO 3 concentration, where germination and crystal growth are slow and the product is mainly monocrystal. In the intermediate range, a mixture of polycrystal and aggregates is obtained. Residence and temperature are also shown to have an effect on the processes (the effect of time being more important than temperature). In the course of this study a bench-scale stripper-crystallizer was developped and operated successfully. (author). tables, graphs

  5. Calcium phosphates: what is the evidence?

    Science.gov (United States)

    Larsson, Sune

    2010-03-01

    A number of different calcium phosphate compounds such as calcium phosphate cements and solid beta-tricalcium phosphate products have been introduced during the last decade. The chemical composition mimics the mineral phase of bone and as a result of this likeness, the materials seem to be remodeled as for normal bone through a cell-mediated process that involves osteoclastic activity. This is a major difference when compared with, for instance, calcium sulphate compounds that after implantation dissolve irrespective of the new bone formation rate. Calcium phosphates are highly biocompatible and in addition, they act as synthetic osteoconductive scaffolds after implantation in bone. When placed adjacent to bone, osteoid is formed directly on the surface of the calcium phosphate with no soft tissue interposed. Remodeling is slow and incomplete, but by adding more and larger pores, like in ultraporous beta-tricalcium phosphate, complete or nearly complete resorption can be achieved. The indications explored so far include filling of metaphyseal fracture voids or bone cysts, a volume expander in conjunction with inductive products, and as a carrier for various growth factors and antibiotics. Calcium phosphate compounds such as calcium phosphate cement and beta-tricalcium phosphate will most certainly be part of the future armamentarium when dealing with fracture treatment. It is reasonable to believe that we have so far only seen the beginning when it comes to clinical applications.

  6. Biosynthesis and characterization of layered iron phosphate

    International Nuclear Information System (INIS)

    Zhou Weijia; He Wen; Wang Meiting; Zhang Xudong; Yan Shunpu; Tian Xiuying; Sun Xianan; Han Xiuxiu; Li Peng

    2008-01-01

    Layered iron phosphate with uniform morphology has been synthesized by a precipitation method with yeast cells as a biosurfactant. The yeast cells are used to regulate the nucleation and growth of layered iron phosphate. The uniform layered structure is characterized by small-angle x-ray diffraction (SAXD), scanning electron microscopy (SEM) and atomic force microscopy (AFM) analyses. Fourier transform infrared spectroscopy (FT-IR) is used to analyze the chemical bond linkages in organic–inorganic hybrid iron phosphate. The likely synthetic mechanism of nucleation and oriented growth is discussed. The electrical conductivity of hybrid iron phosphate heat-treated at different temperatures is presented

  7. [Phosphate-solubilizing activity of aerobic methylobacteria].

    Science.gov (United States)

    Agafonova, N V; Kaparullina, E N; Doronina, N V; Trotsenko, Iu A

    2014-01-01

    Phosphate-solubilizing activity was found in 14 strains of plant-associated aerobic methylobacteria belonging to the genera Methylophilus, Methylobacillus, Methylovorus, Methylopila, Methylobacterium, Delftia, and Ancyclobacter. The growth of methylobacteria on medium with methanol as the carbon and energy source and insoluble tricalcium phosphate as the phosphorus source was accompanied by a decrease in pH due to the accumulation of up to 7 mM formic acid as a methanol oxidation intermediate and by release of 120-280 μM phosphate ions, which can be used by both bacteria and plants. Phosphate-solubilizing activity is a newly revealed role of methylobacteria in phytosymbiosis.

  8. Synthesis of amorphous acid iron phosphate nanoparticles

    International Nuclear Information System (INIS)

    Palacios, E.; Leret, P.; Fernández, J. F.; Aza, A. H. De; Rodríguez, M. A.

    2012-01-01

    A simple method to precipitate nanoparticles of iron phosphate with acid character has been developed in which the control of pH allows to obtain amorphous nanoparticles. The acid aging of the precipitated amorphous nanoparticles favored the P–O bond strength that contributes to the surface reordering, the surface roughness and the increase of the phosphate acid character. The thermal behavior of the acid iron phosphate nanoparticles has been also studied and the phosphate polymerization at 400 °C produces strong compacts of amorphous nanoparticles with interconnected porosity.

  9. Rapid and sensitive Nitrosomonas europaea biosensor assay for quantification of bioavailable ammonium sensu strictu in soil.

    Science.gov (United States)

    Nguyen, Minh Dong; Risgaard-Petersen, Nils; Sørensen, Jan; Brandt, Kristian K

    2011-02-01

    Knowledge on bioavailable ammonium sensu strictu (i.e., immediately available for cellular uptake) in soil is required to understand nutrient uptake processes in microorganisms and thus of vital importance for plant production. We here present a novel ammonium biosensor approach based on the lithoautotrophic ammonia-oxidizing bacterium Nitrosomonas europaea transformed with a luxAB sensor plasmid. Bioluminescence-based ammonium detection was achieved within 10 min with a quantification limit in liquid samples of ∼20 μM and a linear response range up to 400 μM. Biosensor and conventional chemical quantification of ammonium in soil solutions agreed well across a range of sample and assay conditions. The biosensor was subsequently applied for a solid phase-contact assay allowing for direct interaction of biosensor cells with soil particle-associated (i.e., exchangeable plus fixed) ammonium. The assay successfully quantified bioavailable ammonium even in unfertilized soil and demonstrated markedly higher ratios of bioavailable ammonium to water- or 2 M KCl-exchangeable ammonium in anoxic soil than in corresponding oxic soil. Particle-associated ammonium contributed by at least 74% and 93% of the total bioavailable pool in oxic and anoxic soil, respectively. The N. europaea biosensor should have broad relevance for environmental monitoring of bioavailable ammonium and processes depending on ammonium bioavailability.

  10. Aluminum phosphate microcapsule flame retardants for flexible polyurethane foams

    Science.gov (United States)

    Zhang, Bin; Liu, Hong; Han, Jian

    2018-04-01

    In this study, highly efficient flame-retardant aluminum phosphate (ALP) microcapsules were synthesized from ALP and ammonium phosphomolybdate trihydrate. The chemical structure of the ALP microcapsules was characterized by scanning electron microscopy and elemental analysis, and the thermal degradation behavior was investigated by thermogravimetric analysis (TGA). Subsequently, flexible polyurethane (PU) foams were prepared with the ALP microcapsules. Limiting oxygen index (LOI) tests, vertical burning tests, smoke density rating (SDR), and cone calorimetric tests were employed to investigate the combustion of the materials. The results showed that the flexible PU foams with 15 parts per hundred polyol by weight (pphp) ALP microcapsules passed the vertical burning test and they had an increased LOI value of 28.5%. The SDR value for PU/20 pphp ALP microcapsule composites was about 16.0% and the SDR value for the pure PU was about 29.0%. The corresponding flame-retardant mechanism was investigated by Fourier transform infrared spectroscopy, TGA, Pyrolysis Gas Chromatography Mass Spectrometry (Py-GC/MS) tests, and energy-dispersive X-ray spectrometry.

  11. Method of stripping plutonium from tributyl phosphate solution which contains dibutyl phosphate-plutonium stable complexes

    International Nuclear Information System (INIS)

    Ochsenfeld, W.; Schmieder, H.

    1976-01-01

    Fast breeder fuel elements which have been highly burnt-up are reprocessed by extracting uranium and plutonium into an organic solution containing tributyl phosphate. The tributyl phosphate degenerates at least partially into dibutyl phosphate and monobutyl phosphate, which form stable complexes with tetravalent plutonium in the organic solution. This tetravalent plutonium is released from its complexed state and stripped into aqueous phase by contacting the organic solution with an aqueous phase containing tetravalent uranium. 6 claims, 1 drawing figure

  12. Sources et marché du sulfate d'ammonium Sources of and Market for Ammonium Sulfate

    OpenAIRE

    Loussouarn C.; Chauvel A.; Barthel Y.

    2006-01-01

    Engrais azoté le plus utilisé dans le monde jusqu'en 1970, le sulfate d'ammonium ne représente plus aujourd'hui que 4 % de la fertilisation azotée. Avec une teneur en azote de 21 % seulement, il a été peu à peu remplacé comme engrais universel par des produits plus concentrés, notamment l'urée et le nitrate d'ammonium. Obtenu pour plus de 40 % comme sous-produit dans la synthèse de monomères comme le caprolactame, l'acrylonitrile ou le méthacrylate de méthyle, et pour près de 10 % dans le tra...

  13. Efflorescence of ammonium sulfate and coated ammonium sulfate particles: evidence for surface nucleation.

    Science.gov (United States)

    Ciobanu, V Gabriela; Marcolli, Claudia; Krieger, Ulrich K; Zuend, Andreas; Peter, Thomas

    2010-09-09

    Using optical microscopy, we investigated the efflorescence of ammonium sulfate (AS) in aqueous AS and in aqueous 1:1 and 8:1 (by dry weight) poly(ethylene glycol)-400 (PEG-400)/AS particles deposited on a hydrophobically coated slide. Aqueous PEG-400/AS particles exposed to decreasing relative humidity (RH) exhibit a liquid-liquid phase separation below approximately 90% RH with the PEG-400-rich phase surrounding the aqueous AS inner phase. Pure aqueous AS particles effloresced in the RH range from 36.3% to 43.7%, in agreement with literature data (31-48% RH). In contrast, aqueous 1:1 (by dry weight) PEG-400/AS particles with diameters of the AS phase from 7.2 to 19.2 mum effloresced between 26.8% and 33.9% RH and aqueous 8:1 (by dry weight) PEG-400/AS particles with diameters of the AS phase from 1.8 to 7.3 mum between 24.3% and 29.3% RH. Such low efflorescence relative humidity (ERH) values have never been reached before for AS particles of this size range. We show that these unprecedented low ERHs of AS in PEG-400/AS particles could not possibly be explained by the presence of low amounts of PEG-400 in the aqueous AS phase, by a potential inhibition of water evaporation via anomalously slow diffusion through the PEG coating, or by different time scales between various experimental techniques. High-speed photography of the efflorescence process allowed the development of the AS crystallization fronts within the particles to be monitored with millisecond time resolution. The nucleation sites were inferred from the initial crystal growth sites. Analysis of the probability distribution of initial sites of 31 and 19 efflorescence events for pure AS and 1:1 (by dry weight) PEG-400/AS particles, respectively, showed that the particle volume can be excluded as the preferred nucleation site in the case of pure AS particles. For aqueous 1:1 (by dry weight) PEG-400/AS particles preferential AS nucleation in the PEG phase and at the PEG/AS/substrate contact line can be

  14. Dependence of the phosphate sorption capacity on the aluminium and iron in Finnish soils

    Directory of Open Access Journals (Sweden)

    Armi Kaila

    1963-12-01

    Full Text Available An attempt was made to study to what extent the capacity of the more or less acid soils in Finland to sorb phosphate may be explained on the basis of their content of aluminium and iron. The indicator of the phosphate sorption capacity was calculated on the basis of the Freundlich adsorption isotherm according to the procedure proposed by TERÄSVUORI (8. The material consisted of 390 samples from cultivated and virgin soils representing both topsoils and subsoils. The indicator of the phosphate sorption capacity, the coefficient k, varied in the present material from 40 to 1510. The mean values (with the confidence limits at the 95 per cent level were for the 109 samples of sand and fine sand soils 290 ± 17, for the 103 samples of loam and silt soils 201 ± 24, for the 151 clay soils 308 ± 20, and for the 27 humus soils 236 ± 41. The total linear correlation coefficients between k and the soil pH, and its contents of organic carbon or clay were low or negligible in most of the soil groups. The correlation of k with the content of aluminium extracted by Tamm’s acid ammonium oxalate was fairly close in the clay soils (r = 0.84***, lower in the sand and fine sand soils (r = 0.77***, and in the loam and silt soils, and in the humus soils it was rather poor (r = 0.65*** and 0.63*** resp.. The elimination of the effect of the ammonium oxalate soluble iron decreased the correlation in the two latter groups quite markedly (to 0.32** and 0.37 resp., while the corresponding decrease in the coefficients for the former groups was less significant (to 0.64*** and 0.75*** resp.. The elimination of the effect of the ammonium oxalate soluble aluminium, on the other hand, decreased the correlation coefficients between k and the ammonium oxalate soluble iron in the sand and fine sand soils from 0.59*** to 0.26**, in the loam and silt soils from 0.73*** to 0.54***, in the clay soils from 0.70*** to 0.51***, and in the humus soils from 0.68*** to 0.49*. The

  15. The immiscible aqueous solutions of alkyl phosphates. Study for the purpose of uranium extraction from phosphoric acid solutions

    International Nuclear Information System (INIS)

    Mauborgne, Bernard

    1979-01-01

    Systems of immiscible aqueous solutions composed by a phase rich in mineral salt and by another phase almost totally containing an organic salt, have been studied for years, with quaternary ammonium salts with an organic cation. The objective of this research is to study systems symmetric to the previous ones, i.e. with organic anions such as alkyl phosphates, and then to try to understand mechanisms of extraction of metals in these environments. Based on properties of immiscible aqueous solutions, an original three-phase process of liquid-liquid extraction has been developed, and is used to separate uranium in phosphoric acids with better performance than the existing industrial processes [fr

  16. Bio-treatment of phosphate from synthetic wastewater using ...

    African Journals Online (AJOL)

    In this study, the efficient phosphate utilizing isolates were used to remove phosphate from synthetic phosphate wastewater was tested using batch scale process. Hence the objective of the present study was to examine the efficiency of bacterial species individually for the removal of phosphate from synthetic phosphate ...

  17. Bactericidal Specificity and Resistance Profile of Poly(Quaternary Ammonium) Polymers and Protein-Poly(Quaternary Ammonium) Conjugates.

    Science.gov (United States)

    Ji, Weihang; Koepsel, Richard R; Murata, Hironobu; Zadan, Sawyer; Campbell, Alan S; Russell, Alan J

    2017-08-14

    Antibacterial polymers are potentially powerful biocides that can destroy bacteria on contact. Debate in the literature has surrounded the mechanism of action of polymeric biocides and the propensity for bacteria to develop resistance to them. There has been particular interest in whether surfaces with covalently coupled polymeric biocides have the same mechanism of action and resistance profile as similar soluble polymeric biocides. We designed and synthesized a series of poly(quaternary ammonium) polymers, with tailorable molecular structures and architectures, to engineer their antibacterial specificity and their ability to delay the development of bacterial resistance. These linear poly(quaternary ammonium) homopolymers and block copolymers, generated using atom transfer radical polymerization, had structure-dependent antibacterial specificity toward Gram positive and negative bacterial species. When single block copolymers contained two polymer segments of differing antibacterial specificity, the polymer combined the specificities of its two components. Nanoparticulate human serum albumin-poly(quaternary ammonium) conjugates of these same polymers, synthesized via "grafting from" atom transfer radical polymerization, were strongly biocidal and also exhibited a marked decrease in the rate of bacterial resistance development relative to linear polymers. These protein-biocide conjugates mimicked the behavior of surface-presented polycationic biocides rather than their nonproteinaceous counterparts.

  18. effect of two rock phosphates and inoculation with VA mycorrhizae and phosphate solubilizing bacteria on the chickpea-rhizobium symbiosis

    International Nuclear Information System (INIS)

    Soliman, S.M.; Galal, Y.G.M.; El-Ghandour, I.A.

    2004-01-01

    A pot experiment was conducted tracing the effect of two types of phosphorus applied at different rates on the release of nitrogen from fertilizer and its impact on biological nitrogen fixation . chickpea (Cicer Arietinum c v. Cicer 36-ICARDA) was inoculated with peat-based inoculum of phosphorin (Bacillus Megatherium phosphate solubilizing bacteria), Mycorrhizae (VAM) and a mixture of phosphorin and VAM. three types of P fertilizer, i.e.superphosphate, rock P 1 (Safaga) and rock P2 (Abou-Trtour) were applied at rate of 25 and 50 mg Pkg -1 soil in the presence or absence of inoculum. labelled ammonium sulfate with 15 N 10% atom excess was applied at rates of 15 and 30 mg N kg -1 soil for chickpea and barley (reference crop) respectively . Addition of phosphorus fertilizers, especially at the high rates, positively affected the growth and dry weight as compared to the unfertilized control. infections with VAM mixed with phosphorin under low level of rock P (Abou-tarour) gave the highest values of dry weight and N and P uptake when compared with both superphosphate-P source and control. biological N 2 fixed was higher in dual inoculation treatments (i.e.phosphorin +VAM) than those receiving a single inoculum. the percentages of N 2 -fixed ranged from 24 to 53 according to inoculation treatments, P sources and levels

  19. Electrochemically assisted deposition of strontium modified magnesium phosphate on titanium surfaces

    International Nuclear Information System (INIS)

    Meininger, M.; Wolf-Brandstetter, C.; Zerweck, J.; Wenninger, F.; Gbureck, U.; Groll, J.; Moseke, C.

    2016-01-01

    Electrochemically assisted deposition was utilized to produce ceramic coatings on the basis of magnesium ammonium phosphate (struvite) on corundum-blasted titanium surfaces. By the addition of defined concentrations of strontium nitrate to the coating electrolyte Sr 2+ ions were successfully incorporated into the struvite matrix. By variation of deposition parameters it was possible to fabricate coatings with different kinetics of Sr 2+ into physiological media, whereas the release of therapeutically relevant strontium doses could be sustained over several weeks. Morphological and crystallographic examinations of the immersed coatings revealed that the degradation of struvite and the release of Sr 2+ ions were accompanied by a transformation of the coating to a calcium phosphate based phase similar to low-crystalline hydroxyapatite. These findings showed that strontium doped struvite coatings may provide a promising degradable coating system for the local application of strontium or other biologically active metal ions in the implant–bone interface. - Highlights: • Sr-doped struvite coatings have been deposited on titanium by electrochemically assisted deposition. • Sr content can be adjusted by means of process time, current density and pulse mode. • Sr-doped coatings release therapeutically relevant Sr doses in physiological media for several weeks. • During immersion in physiological media Sr-doped struvite coatings transform into a low crystalline calcium phosphate phase.

  20. Spectrophotometric determination of dissolved tri n-butyl phosphate in aqueous streams of Purex process

    International Nuclear Information System (INIS)

    Ganesh, S.; Velavendan, P.; Pandey, N.K.; Ahmed, M.K.; Kamachi Mudali, U.; Natarajan, R.

    2012-01-01

    A spectrophotometric method is developed for the determination of dissolved tri-n butyl phosphate (TBP) in aqueous streams of Purex process used in nuclear fuel reprocessing. The method is based on the formation of phosphomolybdate with added ammonium molybdate followed by reduction with hydrazine sulphate in acid medium. Orthophosphate and molybdate ions combine in acidic solution to give molybdophosphoric (phosphomolybdic) acid, which upon selective reduction (with hydrazinium sulphate) produces a blue colour, due to molybdenum blue. The intensity of blue colour is proportional to the amount of phosphate. If the acidity at the time of reduction is 0.5 M in sulphuric acid and hydrazinium sulphate is the reductant, the resulting blue complex exhibits maximum absorption at 810-840 nm. The system obeys Lambert-Beer's law at 830 nm in the concentration range of 0.1-1.0 μg/mol of phosphate. Molar Absorptivity was determined to be 3.1 x 10 4 L mol -1 cm -1 at 830 nm. The results obtained are reproducible with standard deviation of 1 % and relative error less than 2 % and are in good agreement with those obtained by ion chromatographic technique. (author)

  1. Electrochemically assisted deposition of strontium modified magnesium phosphate on titanium surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Meininger, M. [Department for Functional Materials in Medicine and Dentistry, University of Würzburg, Pleicherwall 2, D-97070 Würzburg (Germany); Wolf-Brandstetter, C. [Max Bergmann Center for Biomaterials, Technical University of Dresden, Budapester Straße 27, D-01069 Dresden (Germany); Zerweck, J.; Wenninger, F.; Gbureck, U.; Groll, J. [Department for Functional Materials in Medicine and Dentistry, University of Würzburg, Pleicherwall 2, D-97070 Würzburg (Germany); Moseke, C., E-mail: claus.moseke@fmz.uni-wuerzburg.de [Department for Functional Materials in Medicine and Dentistry, University of Würzburg, Pleicherwall 2, D-97070 Würzburg (Germany)

    2016-10-01

    Electrochemically assisted deposition was utilized to produce ceramic coatings on the basis of magnesium ammonium phosphate (struvite) on corundum-blasted titanium surfaces. By the addition of defined concentrations of strontium nitrate to the coating electrolyte Sr{sup 2+} ions were successfully incorporated into the struvite matrix. By variation of deposition parameters it was possible to fabricate coatings with different kinetics of Sr{sup 2+} into physiological media, whereas the release of therapeutically relevant strontium doses could be sustained over several weeks. Morphological and crystallographic examinations of the immersed coatings revealed that the degradation of struvite and the release of Sr{sup 2+} ions were accompanied by a transformation of the coating to a calcium phosphate based phase similar to low-crystalline hydroxyapatite. These findings showed that strontium doped struvite coatings may provide a promising degradable coating system for the local application of strontium or other biologically active metal ions in the implant–bone interface. - Highlights: • Sr-doped struvite coatings have been deposited on titanium by electrochemically assisted deposition. • Sr content can be adjusted by means of process time, current density and pulse mode. • Sr-doped coatings release therapeutically relevant Sr doses in physiological media for several weeks. • During immersion in physiological media Sr-doped struvite coatings transform into a low crystalline calcium phosphate phase.

  2. Pentose phosphates in nucleoside interconversion and catabolism.

    Science.gov (United States)

    Tozzi, Maria G; Camici, Marcella; Mascia, Laura; Sgarrella, Francesco; Ipata, Piero L

    2006-03-01

    Ribose phosphates are either synthesized through the oxidative branch of the pentose phosphate pathway, or are supplied by nucleoside phosphorylases. The two main pentose phosphates, ribose-5-phosphate and ribose-1-phosphate, are readily interconverted by the action of phosphopentomutase. Ribose-5-phosphate is the direct precursor of 5-phosphoribosyl-1-pyrophosphate, for both de novo and 'salvage' synthesis of nucleotides. Phosphorolysis of deoxyribonucleosides is the main source of deoxyribose phosphates, which are interconvertible, through the action of phosphopentomutase. The pentose moiety of all nucleosides can serve as a carbon and energy source. During the past decade, extensive advances have been made in elucidating the pathways by which the pentose phosphates, arising from nucleoside phosphorolysis, are either recycled, without opening of their furanosidic ring, or catabolized as a carbon and energy source. We review herein the experimental knowledge on the molecular mechanisms by which (a) ribose-1-phosphate, produced by purine nucleoside phosphorylase acting catabolically, is either anabolized for pyrimidine salvage and 5-fluorouracil activation, with uridine phosphorylase acting anabolically, or recycled for nucleoside and base interconversion; (b) the nucleosides can be regarded, both in bacteria and in eukaryotic cells, as carriers of sugars, that are made available though the action of nucleoside phosphorylases. In bacteria, catabolism of nucleosides, when suitable carbon and energy sources are not available, is accomplished by a battery of nucleoside transporters and of inducible catabolic enzymes for purine and pyrimidine nucleosides and for pentose phosphates. In eukaryotic cells, the modulation of pentose phosphate production by nucleoside catabolism seems to be affected by developmental and physiological factors on enzyme levels.

  3. Removal of phosphate from solution by adsorption and precipitation of calcium phosphate onto monohydrocalcite.

    Science.gov (United States)

    Yagi, Shintaro; Fukushi, Keisuke

    2012-10-15

    The sorption behavior and mechanism of phosphate on monohydrocalcite (CaCO(3)·H(2)O: MHC) were examined using batch sorption experiments as a function of phosphate concentrations, ionic strengths, temperatures, and reaction times. The mode of PO(4) sorption is divisible into three processes depending on the phosphate loading. At low phosphate concentrations, phosphate is removed by coprecipitation of phosphate during the transformation of MHC to calcite. The sorption mode at the low-to-moderate phosphate concentrations is most likely an adsorption process because the sorption isotherm at the conditions can be fitted reasonably with the Langmuir equation. The rapid sorption kinetics at the conditions is also consistent with the adsorption reaction. The adsorption of phosphate on MHC depends strongly on ionic strength, but slightly on temperature. The maximum adsorption capacities of MHC obtained from the regression of the experimental data to the Langmuir equation are higher than those reported for stable calcium carbonate (calcite or aragonite) in any conditions. At high phosphate concentrations, the amount of sorption deviates from the Langmuir isotherm, which can fit the low-to-moderate phosphate concentrations. Speciation-saturation analyses of the reacted solutions at the conditions indicated that the solution compositions which deviate from the Langmuir equation are supersaturated with respect to a certain calcium phosphate. The obtained calcium phosphate is most likely amorphous calcium phosphate (Ca(3)(PO(4))(2)·xH(2)O). The formation of the calcium phosphate depends strongly on ionic strength, temperature, and reaction times. The solubility of MHC is higher than calcite and aragonite because of its metastability. Therefore, the higher solubility of MHC facilitates the formation of the calcium phosphates more than with calcite and aragonite. Copyright © 2012 Elsevier Inc. All rights reserved.

  4. Start-up of simultaneous removal of ammonium and sulfate from an anaerobic ammonium oxidation (anammox) process in an anaerobic up-flow bioreactor

    Energy Technology Data Exchange (ETDEWEB)

    Yang Zhiquan [College of Environmental Science and Engineering, South China University of Technology, Guangzhou, Guangdong 510006 (China); Zhou Shaoqi, E-mail: fesqzhou@scut.edu.cn [College of Environmental Science and Engineering, South China University of Technology, Guangzhou, Guangdong 510006 (China); State Key Laboratory of Subtropical Building Science, South China University of Technology, Guangzhou, Guangdong 510640 (China); Sun Yanbo [College of Environmental Science and Engineering, South China University of Technology, Guangzhou, Guangdong 510006 (China)

    2009-09-30

    A laboratory testing of simultaneous removal of ammonium and sulfate (SRAS) was studied from an anammox process in an anaerobic bioreactor filled with granular activated carbon. Two different phases of experiment were investigated to start up the SRAS process, and final batch tests were performed to analyze the SRAS process. The experiment included an anammox process and an SRAS process. During the anammox process, the highest removal efficiency of ammonium and nitrite was up to 97 and 98%, respectively. After 160 days in the stationary phase of anammox process, the ratio of ammonium to nitrite consumption was approximately 1:1.15, which is much higher than 1:1.32 in the traditional anammox process. The extra electron acceptor, such as sulfate, was thought to react with ammonium by bacteria. Synthetic wastewater containing ammonium chlorine and sodium sulfate was used as the feed for the bioreactor in the second phase of experiment. During the SRAS process, the influent concentrations of ammonium and sulfate were controlled to be 50-60 and 210-240 mg L{sup -1} respectively. After start-up and acclimatization of this process for 60 days, the average effluent concentrations of ammonium and sulfate were 30 and 160 mg L{sup -1}, respectively. The simultaneous ammonium and sulfate removal was detected in the reactor. In order to further validate the biochemical interaction between ammonium and sulfate, batch tests was carried out. Abiotic tests were carried out to demonstrate that the pure chemical action between ammonium and sulfate without microorganism was not possible. Biotic assays with different ammonium and sulfate concentrations were further investigated that high concentrations of ammonium and sulfate could promote simultaneous removal of ammonium and sulfate. And elemental sulfur and nitrogen gas as the products measured in the SRAS process helped to demonstrate the occurrence of new interaction between nitrogen and sulfur. The new process of SRAS in the

  5. Start-up of simultaneous removal of ammonium and sulfate from an anaerobic ammonium oxidation (anammox) process in an anaerobic up-flow bioreactor

    International Nuclear Information System (INIS)

    Yang Zhiquan; Zhou Shaoqi; Sun Yanbo

    2009-01-01

    A laboratory testing of simultaneous removal of ammonium and sulfate (SRAS) was studied from an anammox process in an anaerobic bioreactor filled with granular activated carbon. Two different phases of experiment were investigated to start up the SRAS process, and final batch tests were performed to analyze the SRAS process. The experiment included an anammox process and an SRAS process. During the anammox process, the highest removal efficiency of ammonium and nitrite was up to 97 and 98%, respectively. After 160 days in the stationary phase of anammox process, the ratio of ammonium to nitrite consumption was approximately 1:1.15, which is much higher than 1:1.32 in the traditional anammox process. The extra electron acceptor, such as sulfate, was thought to react with ammonium by bacteria. Synthetic wastewater containing ammonium chlorine and sodium sulfate was used as the feed for the bioreactor in the second phase of experiment. During the SRAS process, the influent concentrations of ammonium and sulfate were controlled to be 50-60 and 210-240 mg L -1 respectively. After start-up and acclimatization of this process for 60 days, the average effluent concentrations of ammonium and sulfate were 30 and 160 mg L -1 , respectively. The simultaneous ammonium and sulfate removal was detected in the reactor. In order to further validate the biochemical interaction between ammonium and sulfate, batch tests was carried out. Abiotic tests were carried out to demonstrate that the pure chemical action between ammonium and sulfate without microorganism was not possible. Biotic assays with different ammonium and sulfate concentrations were further investigated that high concentrations of ammonium and sulfate could promote simultaneous removal of ammonium and sulfate. And elemental sulfur and nitrogen gas as the products measured in the SRAS process helped to demonstrate the occurrence of new interaction between nitrogen and sulfur. The new process of SRAS in the inorganic

  6. Cyanotoxins: a poison that frees phosphate.

    Science.gov (United States)

    Raven, John A

    2010-10-12

    Autotrophic organisms obtain phosphorus from the environment by secreting alkaline phosphatases that act on esters, resulting in inorganic phosphate that is then taken up. New work shows that the cyanobacterium Aphanizomenon ovalisporum obtains inorganic phosphate by secreting the cyanotoxin cylindrospermopsin, which induces alkaline phosphatase in other phytoplankton species. Copyright © 2010 Elsevier Ltd. All rights reserved.

  7. Phosphate recycling in the phosphorus industry

    NARCIS (Netherlands)

    Schipper, W.J.; Klapwijk, A.; Potjer, A.; Rulkens, W.H.; Temmink, B.G.; Kiestra, F.D.G.; Lijmbach, A.C.M.

    2001-01-01

    The feasibility of phosphate recycling in the white phosphorus production process is discussed. Several types of materials may be recycled, provided they are dry inorganic materials, low in iron, copper and zinc. Sewage sludge ash may be used if no iron is used for phosphate precipitation in the

  8. Photoelectron spectroscopy of phosphites and phosphates

    Energy Technology Data Exchange (ETDEWEB)

    Chattopadhyay, S.; Findley, G.L.; McGlynn, S.P.

    1981-01-01

    The ultraviolet photoelectron spectra (UPS) of trimethyl and triethyl phosphite, trimethyl and triethyl phosphate and four substituted phosphates are presented. Assignments are based on analogies to the UPS of phosphorus trichloride and phosphoryl trichloride and are substantiated by CNDO/2 computations. The mechanisms of P-O (axial) bond formation is discussed.

  9. Phosphate recycling in the phosphorus industry

    NARCIS (Netherlands)

    Schipper, W.J.; Klapwijk, A.; Potjer, B.; Rulkens, W.H.; Temmink, B.G.; Kiestra, F.D.G.; Lijmbach, A.C.M.

    2004-01-01

    The article describes the potential and limitations for recovery of phosphate from secondary materials in the production process for white phosphorus. This thermal process involves the feeding of phosphate rock, cokes and pebbles to a furnace. The reducing conditions in the furnace promote the

  10. Rock phosphate solubilization by the ectomycorrhizal fungus ...

    African Journals Online (AJOL)

    SAM

    2014-06-18

    Jun 18, 2014 ... To evaluate phosphate solubilization of ... and MHB had the potential to solubilize these phosphates by decreasing the pH and confirmed that ... Minerals like N, P, K, Ca, S, Zn, Cu and Sr are ... sterile distilled water, chopped, homogenized in 10 ml sterile .... The role of carbon source is important in mineral.

  11. Genetics Home Reference: glucose phosphate isomerase deficiency

    Science.gov (United States)

    ... glycolytic pathway; in this step, a molecule called glucose-6-phosphate is converted to another molecule called fructose-6-phosphate. When GPI remains a single molecule (a monomer) it is involved in the development and maintenance of nerve cells ( neurons ). In this context, it is often known as ...

  12. Low-temperature setting phosphate ceramics for stabilization of DOE problem low level mixed-waste: I. Material and waste form development

    International Nuclear Information System (INIS)

    Singh, D.; Wagh, A.; Knox, L.; Mayberry, J.

    1994-03-01

    Chemically bonded phosphate ceramics are proposed as candidates for solidification and stabilization of some of the open-quotes problemclose quotes DOE low-level mixed wastes at low-temperatures. Development of these materials is crucial for stabilization of waste streams which have volatile species and any use of high-temperature technology leads to generation of off-gas secondary waste streams. Several phosphates of Mg, Al, and Zr have been investigated as candidate materials. Monoliths of these phosphates were synthesized using chemical routes at room or slightly elevated temperatures. Detailed physical and chemical characterizations have been conducted on some of these phosphates to establish their durability. Magnesium ammonium phosphate has shown to possess excellent mechanical and as well chemical properties. These phosphates were also used to stabilize a surrogate ash waste with a loading ranging from 25-35 wt.%. Characterization of the final waste forms show that waste immobilization is due to both chemical stabilization and physical encapsulation of the surrogate waste which is desirable for waste immobilization

  13. 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

    Energy Technology Data Exchange (ETDEWEB)

    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.

  14. Mineral phosphate solubilizing bacterial community in agro-ecosystem

    African Journals Online (AJOL)

    STORAGESEVER

    2009-12-15

    Dec 15, 2009 ... patterns. Four insoluble phosphate sources; purulia rock phosphate (PRP), mussourie rock phosphate. (MRP) ... community composition analysis (Garland, 1996a) and ..... the threshold level that enabled only a few species to.

  15. Investigation by gamma-ray spectrometry and INAA of radioactivity impact on phosphate fertilizer plant environment

    International Nuclear Information System (INIS)

    Pantelica, A.; Companis, I.; Georgescu, I. I.; Pincovshi, E.

    2006-01-01

    The radioactive polluting effect of a phosphate fertilizer plant on the environment was investigated by gamma-ray spectrometry and neutron activation analysis (INAA). The hazards could arise from industrial plants using raw phosphate materials to prepare fertilizers for agricultural purposes due to the phosphate rock which, depending on the type and geographical zone of provenance may contain rather large amounts of uranium. The fertilizer plant under study is situated about 4 km from the town of Turnu Magurele, on the left bank of the Danube River in Romania. The main by-products of the factory are: nitro phosphate type fertilizers (NP, NPK), Ammonia, Nitric acid, Ammonium nitrate, Urea, Sulfuric acid, Phosphoric acid, Sodium fluorosilicate and Aluminum sulfate. Gamma-ray spectrometry was used to determine activity concentrations of naturally occurring radionuclides ( 2 26Ra, 2 35U, 2 38U, 2 32Th, and 4 0K), as well as 1 37Cs man-made radionuclide in surface soils collected from semicircular areas within radii of 0.5 and 15 km of the plant; in addition, different NPK type fertilizers and phosphate rocks were investigated. The samples (mass of about 100-g each) were kept tightly closed for one month to permit 2 26Ra to establish radioactive equilibrium with its decay products. This method makes it possible to assess U, Th, and K contents in samples by measuring 2 38U and 2 32Th (in equilibrium with their radioactive daughters) and 4 0K radioactivity, taken into account that 1 g of U, Th and K yield 1 2358 Bq 2 38U, 569 Bq 2 35U, 4057.2 Bq 2 32Th and 33.11 Bq 4 0K, respectively. The spectrometrical chain was based on a HPGe (EG and G Ortec) detector of 30 % relative efficiency and 2.1 keV resolution at 1332 keV of 6 0Co. INAA technique (neutron irradiation at TRIGA reactor of SCN Pitesti) was used to determine macro, micro and trace elements in samples collected from both technological shops of the factory (air dust and drinking tap water) and its surroundings

  16. Urea cycle pathway targeted therapeutic action of naringin against ammonium chloride induced hyperammonemic rats.

    Science.gov (United States)

    Ramakrishnan, Arumugam; Vijayakumar, Natesan

    2017-10-01

    Ammonia is a well-known neurotoxin that causes liver disease and urea cycle disorder. Excessive ammonia content in the blood leads to hyperammonemic condition and affects both excitatory and inhibitory neurotransmission including brain edema and coma. Naringin, a plant bioflavonoid present in various citrus fruits and mainly extracted from the grape fruit. This study was designed to assess the protective effect of naringin on ammonium chloride (NH 4 Cl) induced hyperammonemic rats. Experimental hyperammonemia was induced by intraperitoneal injections (i.p) of NH 4 Cl (100mg/kg body weight (b.w.)) thrice a week for 8 consecutive weeks. Hyperammonemic rats were treated with naringin (80mg/kg b.w.) via oral gavage. Naringin administration significantly augmented the level of blood ammonia and plasma urea. Naringin also upregulate the expression of urea cycle enzymes such as carbamoyl phosphate synthase I (CPS I) and ornithine transcarbamylase (OTC), arininosuccinate synthase (ASS), argininosuccinate lyase (ASL) and arginase I (ARG) and metabotropic glutamate receptors (mGluRs) such as mGluRs I and mGluRs V and down regulate the expression of inflammatory markers like tumor necrosis factor (TNF-α), nuclear factor kappa B (NF-kB), Interleukin-6 (IL-6), inducible nitric oxide synthase (iNOS). In addition, to this, the protective effect of naringin was also revealed through the immunohistochemical changes in tissues. Thus our present study result suggest that naringin modulates the expression of proteins involved in urea cycle pathway and suppresses the expression of inflammatory markers and acts as a potential agent to treat condition in rats. Copyright © 2017 Elsevier Masson SAS. All rights reserved.

  17. Ammonium uptake by phytoplankton regulates nitrification in the sunlit ocean.

    Directory of Open Access Journals (Sweden)

    Jason M Smith

    Full Text Available 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.

  18. CRYSTALLIZATION KINETICS OF AMMONIUM PERCHLORATE IN AN AGITATED VESSEL

    Directory of Open Access Journals (Sweden)

    Nahidh Kaseer

    2013-05-01

    Full Text Available 31Overall crystal growth kinetics for ammonium perchlorate in laboratory scale batch  agitated vessel crystallizer have been determined from batch experiments performed in an integral mode. The effects of temperature between 30-60ºC, seed size 0.07, 0.120 and 0.275 mm and stirrer speed 160, 340, and 480 rpm, on the kinetics of crystal growth were investigated. Two different methods, viz. polynomial fitting and initial derivative were used to predict the kinetics expression. In general both methods gave comparable results for growth kinetics estimation. The order of growth process is not more than two. The activation energy for crystal growth of ammonium perchlorate was determined and found  to be equal to 5.8 kJ/ mole.            Finally, the influence of the affecting parameters on the crystal growth rate gives general expression that had an obvious dependence of the growth rate on each variables of concern (temperature, seed size, and stirrer speed .The general overall growth rate expression had shown that super saturation is the most significant variable. While the positive dependence of the stirrer speed demonstrates the importance of the diffusional step in the growth rate model. Moreover, the positive dependence of the seed size demonstrate the importance of the surface integration  step in the growth rate model. All the studied variables tend to suggest that the growth rate characteristics  of ammonium perchlorate from aqueous solution commenced in a batch crystallizer are diffusion kinetic controlled process.

  19. Regeneration of clinoptilolite zeolite used for the ammonium removal

    International Nuclear Information System (INIS)

    Garcia G, M.C.

    2002-01-01

    The use of zeolites has been increased in the last years with different applications and with a great boom in the environmental area, but a little had been make about the regeneration of such zeolites. The presence of nitrogen-ammonia in water may cause serious pollution problems since it results to be toxic for fishes and other aquatic life forms, also it provokes the algae growing. The natural clinoptilolite contains interchangeable ions such as the sodium (Na + ), potassium (K + ), magnesium (Mg 2+ ) and calcium (Ca 2+ ) in different proportions depending on the mineral origin When the zeolite is upgraded to its sodium form, the cation exchange capacity and the preference by the nitrogen-ammonia are increased, allowing the reversible process of sorption. In this work it was proposed the regeneration to its sodium form about the ammonia clinoptilolite zeolite. The natural mineral was characterized using the methods such as: X-ray diffraction, Infrared spectroscopy, Thermal gravimetric analysis and surface area. The results show that the ammonium sorption was between 95% and 98.7% such an ambient temperature as a flow back. the zeolite was regenerated approximately from 60% in the first cycle up to 97% in the last cycle at flow back temperature and of 59.2% up to 96.9% at ambient temperature, it was not presented any significant effect which could be attributed to the temperature. During the exchange process, the cations present in the natural zeolite were exchanged with the ammonium ions, this process was not completed due to that retained ammonium quantity was major that of the desorpted ions, what shows that in addition of ion exchange, another type of sorption process exists. (Author)

  20. Spectrographic determination of impurities in ammonium hydrogen fluoride samples

    International Nuclear Information System (INIS)

    Roca, M.; Capdevila, C.; Alduan, F.A.

    1976-01-01

    The quantitative spectrographic trace determination of Al, B, Cr, Cu, Fe, Mn, Mo, Ni, Pb and Si in ammonium hydrogen fluoride samples is considered. 10 A dc arc excitation and graphite electrodes with crate either 4.5 mm or 8 mm deep are employed. A comparison of various matrices such as graphite, gallium oxide, germanium oxide, magnesium oxide and zinc oxide, in the ratios 1:1 and 1:3, as well as a mixture 50% graphite - 50% zinc oxide in the ratio 1:1 is included. Zinc oxide in the ratio 1:1 and 4x8 mm craters show the best over-all results. (author)

  1. Dielectric properties of a potassium nitrate–ammonium nitrate system

    OpenAIRE

    Alexey Yu. Milinskiy; Anton A. Antonov

    2015-01-01

    Potassium nitrate has a rectangular hysteresis loop and is thought to be a promising material for non-volatile ferroelectric memory. However, its polar phase is observed in a narrow temperature range. This paper deals with an effect of ammonium nitrate NH4NO3 on the dielectric properties of potassium nitrate. Thermal dependencies of the linear dielectric permittivity ε and the third-harmonic coefficient g3 for potassium nitrate and polycrystalline binary (KNO3)1–x(NH4NO3)x system (x = 0.025, ...

  2. Surface energy and crystallization phenomena of ammonium dinitramide

    Energy Technology Data Exchange (ETDEWEB)

    Teipel, Ulrich; Heintz, Thomas [Fraunhofer-Institut fuer Chemische Technologie (ICT), PO Box 1240, D-76318 Pfinztal (Germany)

    2005-12-01

    Ammonium dinitramide (ADN) was characterized during recrystallization from the melt. The surface tension of molten ADN at 97 C was measured to be 89 mN/m. The wetting angles between molten ADN and different solid surfaces (polytetrafluoroethylene, glass, steel, and aluminum) were determined. The wettability depends on the surface tension of molten ADN, the free surface energy of the solid surfaces and the interfacial tension between the solid and liquid. Observations of the recrystallization behavior of molten ADN showed that nucleation does not occur, even at super cooling rates of 70 K. Crystallization can be initiated by the application of seed crystals. (Abstract Copyright [2005], Wiley Periodicals, Inc.)

  3. Ammonium Bifluoride Poisoning: Our Eight-year Experiences

    OpenAIRE

    Serkan Özsoylu; Başak Akyıldız; Adem Dursun

    2018-01-01

    Introduction: The aim of the study was to discuss clinical effects, treatment options and outcomes of pediatric ammonium bifluoride (ABF) poisoning. Methods: This study was designed as retrospective case series. We analyzed the medical records of children who were hospitalized for ABF poisoning between January 2009 and October 2017. Results: The median calcium level on arrival to the hospital was 9.26 mg/dL (minimum-maximum: 4.6-10.9). The median calcium level 2 hours after arrival was ...

  4. The Properties of Ammonium Dinitramine (ADN): Part 2: Melt Casting

    Science.gov (United States)

    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.

  5. Ammonium diamminesilver(I bis(5-chloro-2-hydroxybenzenesulfonate trihydrate

    Directory of Open Access Journals (Sweden)

    Zhao-Peng Deng

    2012-02-01

    Full Text Available The reaction of silver nitrate with 5-chloro-2-hydroxybenzenesulfonic acid in the presence of ammonia yielded the title salt, (NH4[Ag(NH32](C6H4ClO4S2·3H2O. The AgI ion shows linear coordination [N—Ag—N = 175.2 (1 °]. The ammonium and diamminesilver cations, the benzenesulfonate anion and the lattice water molecules interact through an intricate network of N—H...O and O—H...O hydrogen bonds to form a three-dimensional network.

  6. A study on chlorination of uranium metal using ammonium chloride

    International Nuclear Information System (INIS)

    Eun, H.C.; Kim, T.J.; Jang, J.H.; Kim, G.Y.; Lee, S.J.; Hur, J.M.

    2017-01-01

    In this study, the chlorination of uranium metal using ammonium chloride (NH 4 Cl) was conducted to derive an easy and simple uranium chloride production method without impurities. In thermodynamic equilibrium calculations, it was predicted that only uranium chlorides can be produced by the reactions between uranium metal and NH 4 Cl. Experimental conditions for the chlorination of uranium metal were determined using a chlorination test of cerium metal using NH 4 Cl. It was confirmed that UCl 3 and UCl 4 in the form of particles as uranium chlorination products can be obtained from the chlorination method using NH 4 Cl. (author)

  7. Sonochemical precipitation of amorphous uranium phosphates from trialkyl phosphate solutions and their thermal conversion to UP2O7

    Czech Academy of Sciences Publication Activity Database

    Doroshenko, I.; Žurková, J.; Moravec, Z.; Bezdička, Petr; Pinkas, J.

    2015-01-01

    Roč. 26, SEP (2015), s. 157-162 ISSN 1350-4177 Institutional support: RVO:61388980 Keywords : Uranium * Phosphates * Sonochemistry * Nuclear waste * Trimethyl phosphate * Triethyl phosphate Subject RIV: CA - Inorganic Chemistry Impact factor: 4.556, year: 2015

  8. A Mycorrhizal-Specific Ammonium Transporter from Lotus japonicus Acquires Nitrogen Released by Arbuscular Mycorrhizal Fungi1

    Science.gov (United States)

    Guether, Mike; Neuhäuser, Benjamin; Balestrini, Raffaella; Dynowski, Marek; Ludewig, Uwe; Bonfante, Paola

    2009-01-01

    In mycorrhizal associations, the fungal partner assists its plant host by providing nitrogen (N) in addition to phosphate. Arbuscular mycorrhizal (AM) fungi have access to inorganic or organic forms of N and translocate them via arginine from the extra- to the intraradical mycelium, where the N is transferred to the plant without any carbon skeleton. However, the molecular form in which N is transferred, as well as the involved mechanisms, is still under debate. NH4+ seems to be the preferential transferred molecule, but no plant ammonium transporter (AMT) has been identified so far. Here, we offer evidence of a plant AMT that is involved in N uptake during mycorrhiza symbiosis. The gene LjAMT2;2, which has been shown to be the highest up-regulated gene in a transcriptomic analysis of Lotus japonicus roots upon colonization with Gigaspora margarita, has been characterized as a high-affinity AMT belonging to the AMT2 subfamily. It is exclusively expressed in the mycorrhizal roots, but not in the nodules, and transcripts have preferentially been located in the arbusculated cells. Yeast (Saccharomyces cerevisiae) mutant complementation has confirmed its functionality and revealed its dependency on acidic pH. The transport experiments using Xenopus laevis oocytes indicated that, unlike other plant AMTs, LjAMT2;2 transports NH3 instead of NH4+. Our results suggest that the transporter binds charged ammonium in the apoplastic interfacial compartment and releases the uncharged NH3 into the plant cytoplasm. The implications of such a finding are discussed in the context of AM functioning and plant phosphorus uptake. PMID:19329566

  9. Are Polyphosphates or Phosphate Esters Prebiotic Reagents?

    Science.gov (United States)

    Keefe, Anthony D.; Miller, Stanley L.

    1995-01-01

    It is widely held that there was a phosphate compound in prebiotic chemistry that played the role of adenosine triphosphate and that the first living organisms had ribose-phosphate in the backbone of their genetic material. However, there are no known efficient prebiotic synthesis of high-energy phosphates or phosphate esters. We review the occurrence of phosphates in nature, the efficiency of the volcanic synthesis of P4O10, the efficiency of polyphosphate synthesis by heating phosphate minerals under geological conditions, and the use of high-energy organic compounds such as cyanamide or hydrogen cyanide. These are shown to be inefficient processes especially when the hydrolysis of the polyphosphates is taken into account. For example, if a whole atmosphere of methane or carbon monoxide were converted to cyanide which somehow synthesized polyphosphates quantitatively, the polyphosphate concentration in the ocean would still have been insignificant. We also attempted to find more efficient high-energy polymerizing agents by spark discharge syntheses, but without success. There may still be undiscovered robust prebiotic syntheses of polyphosphates, or mechanisms for concentrating them, but we conclude that phosphate esters may not have been constituents of the first genetic material. Phosphoanhydrides are also unlikely as prebiotic energy sources.

  10. Copolymerization of poly (ethylene oxide) and poly (methyl methacrylate) initiated by ceric ammonium nitrate

    International Nuclear Information System (INIS)

    Gomes, A.S.; Ferreira, A.A.; Coutinho, F.M.B.; Marinho, J.R.D.

    1984-01-01

    Cerium (IV) salts such as the ceric ammonium nitrate and ceric ammonium sulfate in aqueous acid solution with reducing agents such as alcohols, thiols, glycols, aldehydes and amines are well known initiators of vinyl polymerization. In this work, the polymerization of methyl methacrylate initiated by ceric ammonium nitrate/HNO 3 -poly(ethylene oxide) with hydroxyl end group system was studied in aqueous solution at 25 0 C to obtain block copolymers. (Author) [pt

  11. Dissimilatory nitrate reduction to nitrate, nitrous oxide, and ammonium by Pseudomonas putrefaciens.

    OpenAIRE

    Samuelsson, M O

    1985-01-01

    The influence of redox potential on dissimilatory nitrate reduction to ammonium was investigated on a marine bacterium, Pseudomonas putrefaciens. Nitrate was consumed (3.1 mmol liter-1), and ammonium was produced in cultures with glucose and without sodium thioglycolate. When sodium thioglycolate was added, nitrate was consumed at a lower rate (1.1 mmol liter-1), and no significant amounts of nitrite or ammonium were produced. No growth was detected in glucose media either with or without sod...

  12. Relations of ammonium minerals at several hydrothermal systems in the western U.S.

    Science.gov (United States)

    Krohn, M.D.; Kendall, C.; Evans, J.R.; Fries, T.L.

    1993-01-01

    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 NH4+ 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. ?? 1993.

  13. Ammonia volatilization from surface-applied nitrogen solution of urea and ammonium nitrate

    International Nuclear Information System (INIS)

    Trivellin, Paulo Cezar Ocheuze; Stefanutti, Ronaldo; Lima Filho, Oscar Fontvo de; Tziboy, Edgar Alfredo Tzi; Oliveira Junior, Jovo Alberto de; Bendassolli, Jose Albertino

    1996-08-01

    The urea is one of the fertilizers more utilized in modern agriculture. One of the problems in the urea utilization is the ammonium volatilization, resulting in low utilization of N-fertilizers by the plants.The objective of this study it was to evaluate and to compare in laboratories conditions , utilizing the 15 N technic the soil's ammonium lost by volatilization associated a superficial application of nitrogen corresponding doses like urea solution and urea and ammonium nitrates solution

  14. Effects of Calcium Lignosulfonate and Silicic Acid on Ammonium Nitrate Degradation

    Directory of Open Access Journals (Sweden)

    Ahmet Ozan Gezerman

    2014-01-01

    Full Text Available Ammonium nitrate salts are the most commonly used nitrogenous fertilizers in industry. However, storage of ammonium nitrate is problematic, since its initial properties can decline because of environmental factors, leading to large economic losses. In this study, in order to prevent the caking and degradation of ammonium nitrate, an alternative composition with additional calcium lignosulfonate and silicic acid was studied. The resulting fertilizer was analyzed by screening analysis, ion chromatography, and electron microscopy methods.

  15. Enhanced sulfidation xanthate flotation of malachite using ammonium ions as activator

    OpenAIRE

    Dandan Wu; Wenhui Ma; Yingbo Mao; Jiushuai Deng; Shuming Wen

    2017-01-01

    In this study, ammonium ion was used to enhance the sulfidation flotation of malachite. The effect of ammonium ion on the sulfidation flotation of malachite was investigated using microflotation test, inductively coupled plasma (ICP) analysis, zeta potential measurements, and scanning electron microscope analysis (SEM). The results of microflotation test show that the addition of sodium sulfide and ammonium sulfate resulted in better sulfidation than the addition of sodium sulfide alone. The ...

  16. The Comparison of Ammonium or Nitrate-Grown Lettuce and Spinach in a Hydroponic System

    OpenAIRE

    H. R. Roosta

    2010-01-01

    Most plant species are sensitive to high ammonium concentrations. In this experiment the sensitivity of lettuce and spinach to ammonium was investigated. In a factorial experiment with framework of a completely randomized design with two factors, nitrogen form (ammonium and nitrate) and plant species (lettuce and spinach), and three replications seeds were germinated in a mixture of perlite, sand and clay in soil-maid pots. After two weeks, the seedlings at two true-leaf stage were then trans...

  17. How do arbuscular mycorrhizal fungi handle phosphate? New insight into fine-tuning of phosphate metabolism.

    Science.gov (United States)

    Ezawa, Tatsuhiro; Saito, Katsuharu

    2018-04-27

    Contents Summary I. Introduction II. Foraging for phosphate III. Fine-tuning of phosphate homeostasis IV. The frontiers: phosphate translocation and export V. Conclusions and outlook Acknowledgements References SUMMARY: Arbuscular mycorrhizal fungi form symbiotic associations with most land plants and deliver mineral nutrients, in particular phosphate, to the host. Therefore, understanding the mechanisms of phosphate acquisition and delivery in the fungi is critical for full appreciation of the mutualism in this association. Here, we provide updates on physical, chemical, and biological strategies of the fungi for phosphate acquisition, including interactions with phosphate-solubilizing bacteria, and those on the regulatory mechanisms of phosphate homeostasis based on resurveys of published genome sequences and a transcriptome with reference to the latest findings in a model fungus. For the mechanisms underlying phosphate translocation and export to the host, which are major research frontiers in this field, not only recent advances but also testable hypotheses are proposed. Lastly, we briefly discuss applicability of the latest tools to gene silencing in the fungi, which will be breakthrough techniques for comprehensive understanding of the molecular basis of fungal phosphate metabolism. © 2018 The Authors. New Phytologist © 2018 New Phytologist Trust.

  18. Phosphate Solubilizers from the Rhizosphere of Piper nigrum L. in Karnataka, India Solubilizadores de Fosfatos desde la Rizósfera de Piper nigrum L. en Karnataka, India

    Directory of Open Access Journals (Sweden)

    Usha Seshachala

    2012-09-01

    Full Text Available Black pepper (Piper nigrum L. is a climbing vine known for its pungent fruit used as a spice worldwide. The aim of this study was to evaluate the available P content in the native soils where pepper is grown as a crop plant. The native population of phosphate solubilising microbes (PSM was studied from the rhizosphere of P. nigrum plants grown in the Western Ghats of Karnataka, India. A variety of phosphate solubilising bacteria and fungi were isolated from the rhizosphere soil samples. Phosphate solubilising capacity of different isolates was studied on Pikovskaya's medium. The isolates were tested for their phosphate solubilising capacity in vitro with three different phosphate sources, tricalcium phosphate (TCP, potassium dihydrogen phosphate (KHP, and rock phosphate (RP in the concentrations 2.5, 5.0 and 7.5 g L-1. The three phosphate sources were solubilised by the isolates in varying proportions. The dominant PSM flora obtained from the samples included Bacillus and Aspergillus. The study showed that PSM utilised the three phosphate sources TCP, KHP, and RP with considerable variability. The phosphatase activity of the isolates showed that the predominant microorganisms were Bacillus subtilis (5.33 U mL-1 and Aspergillus (11.5 U mL¹. The predominant organisms were identified up to molecular level.La pimienta negra (Piper nigrum L. es una planta trepadora conocida por su fruto utilizado como especia en todo el mundo. El objetivo de este estudio fue evaluar el contenido de P disponible en los suelos nativos donde se cultiva. La población nativa de microbios solubilizantes de fosfato (PSM fue estudiada en la rizósfera de plantas de P. nigrum cultivadas en los Ghats occidentales de Karnataka, India. Una variedad de hongos y bacterias solubilizantes de fosfato fueron aislados de muestras de suelo de la rizósfera. La capacidad solubilizadora de fosfato de diferentes aislamientos fue estudiada en medio de Pikovskaya. Los aislados fueron

  19. Effect of phosphate additive on the nitrogen transformation during pig manure composting.

    Science.gov (United States)

    Wu, Juan; He, Shengzhou; Liang, Ying; Li, Guoxue; Li, Song; Chen, Shili; Nadeem, Faisal; Hu, Jingwei

    2017-07-01

    Previous studies revealed that phosphate, as an additive to composting, could significantly reduce NH 3 emission and nitrogen loss through change of pH and nitrogen fixation to form ammonium phosphate. However, few studies have explored the influence of pH change and phosphate additive on NO x - -N, NH 4 + -N, NH 3 , and N 2 O, which are dominate forms of nitrogen in composting. In this study, the equimolar H 3 PO 4 , H 2 SO 4 , and K 2 HPO 4 were added into pig manure composting to evaluate the effect of H + and PO 4 3- on nitrogen transformation. As a result, we reached the conclusion that pH displays significant influence on adsorption from PO 4 3- to NH 4 + . The NH 4 + -N concentration in H 3 PO 4 treatment kept over 3 g kg -1 DM (dry matter) which is obviously higher than that in H 2 SO 4 treatment, and NH 4 + -N concentration in K 2 HPO 4 treatment (pH>8.5) is lower than 0.5 g kg -1 DM because adsorption capacity of PO 4 3- is greatly weakened and NH 4 + -N rapidly transformed to NH 3 -N influenced by high pH value. The N 2 O emission of composting is significantly correlated with incomplete denitrification of NO x - -N, and PO 4 3- addition could raise NO x - -N contents to restrict denitrification and further to promote N 2 O emission. The study reveals the influence mechanism of phosphate additive to nitrogen transformation during composting, presents theoretical basis for additive selection in nitrogen fixation, and lays foundation for study about nitrogen circulation mechanism during composting.

  20. Arctic water tracks retain phosphorus and transport ammonium

    Science.gov (United States)

    Harms, T.; Cook, C. L.; Wlostowski, A. N.; Godsey, S.; Gooseff, M. N.

    2017-12-01

    Hydrologic flowpaths propagate biogeochemical signals among adjacent ecosystems, but reactions may attenuate signals by retaining, removing, or transforming dissolved and suspended materials. The theory of nutrient spiraling describes these simultaneous reaction and transport processes, but its application has been limited to stream channels. We applied nutrient spiraling theory to water tracks, zero-order channels draining Arctic hillslopes that contain perennially saturated soils and flow at the surface either perennially or in response to precipitation. In the Arctic, experimental warming results in increased availability of nitrogen, the limiting nutrient for hillslope vegetation at the study site, which may be delivered to aquatic ecosystems by water tracks. Increased intensity of rain events, deeper snowpack, earlier snowmelt, and increasing thaw depth resulting from climate change might support increased transport of nutrients, but the reactive capacity of hillslope flowpaths, including sorption and uptake by plants and microbes, could counter transport to regulate solute flux. Characteristics of flowpaths might influence the opportunity for reaction, where slower flowpaths increase the contact time between solutes and soils or roots. We measured nitrogen and phosphorus uptake and transient storage of water tracks through the growing season and found that water tracks retain inorganic phosphorus, but transport ammonium. Nutrient uptake was unrelated to transient storage, suggesting high capacity for nutrient retention by shallow organic soils and vegetation. These observations indicate that increased availability of ammonium, the biogeochemical signal of warming tundra, is propagated by hillslope flowpaths, whereas water tracks attenuate delivery of phosphorus to aquatic ecosystems, where its availability typically limits production.

  1. Ammonium-tungstate-promoted growth of boron nitride nanotubes

    Science.gov (United States)

    E, Songfeng; Li, Chaowei; Li, Taotao; Geng, Renjie; Li, Qiulong; Lu, Weibang; Yao, Yagang

    2018-05-01

    Ammonium tungstate ((NH4)10W12O41 · xH2O) is a kind of oxygen-containing ammonium salt. The following study proves that it can be successfully used as a metal oxide alternative to produce boron oxide (B2O2) by oxidizing boron (B) in a traditional boron oxide chemical vapor deposition (BOCVD) process. This special oxidant promotes the simplistic fabrication of boron nitride nanotubes (BNNTs) in a conventional horizontal tube furnace, an outcome which may have resulted from its strong oxidizability. The experimental results demonstrate that the mole ratio of B and (NH4)10W12O41 · xH2O is a key parameter in determining the formation, quality and quantity of BNNTs when stainless steel is employed as a catalyst. We also found that Mg(NO3)2 and MgO nanoparticles (NPs) can be used as catalysts to grow BNNTs with the same precursor. The BNNTs obtained from the Mg(NO3)2 catalyst were straighter than those obtained from the MgO NP catalyst. This could have been due to the different physical forms of the catalysts that were used.

  2. Turbulence and Cavitation Suppression by Quaternary Ammonium Salt Additives.

    Science.gov (United States)

    Naseri, Homa; Trickett, Kieran; Mitroglou, Nicholas; Karathanassis, Ioannis; Koukouvinis, Phoevos; Gavaises, Manolis; Barbour, Robert; Diamond, Dale; Rogers, Sarah E; Santini, Maurizio; Wang, Jin

    2018-05-16

    We identify the physical mechanism through which newly developed quaternary ammonium salt (QAS) deposit control additives (DCAs) affect the rheological properties of cavitating turbulent flows, resulting in an increase in the volumetric efficiency of clean injectors fuelled with diesel or biodiesel fuels. Quaternary ammonium surfactants with appropriate counterions can be very effective in reducing the turbulent drag in aqueous solutions, however, less is known about the effect of such surfactants in oil-based solvents or in cavitating flow conditions. Small-angle neutron scattering (SANS) investigations show that in traditional DCA fuel compositions only reverse spherical micelles form, whereas reverse cylindrical micelles are detected by blending the fuel with the QAS additive. Moreover, experiments utilising X-ray micro computed tomography (micro-CT) in nozzle replicas, quantify that in cavitation regions the liquid fraction is increased in the presence of the QAS additive. Furthermore, high-flux X-ray phase contrast imaging (XPCI) measurements identify a flow stabilization effect in the region of vortex cavitation by the QAS additive. The effect of the formation of cylindrical micelles is reproduced with computational fluid dynamics (CFD) simulations by including viscoelastic characteristics for the flow. It is demonstrated that viscoelasticity can reduce turbulence and suppress cavitation, and subsequently increase the injector's volumetric efficiency.

  3. Thermophysical properties of sulfonium- and ammonium-based ionic liquids.

    Science.gov (United States)

    Bhattacharjee, Arijit; Luís, Andreia; Lopes-da-Silva, José A; Freire, Mara G; Carvalho, Pedro J; Coutinho, João A P

    2014-11-15

    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, [N 4111 ][NTf 2 ], tributylmethylammonium bis(trifluoromethylsulfonyl)imide, [N 4441 ][NTf 2 ], diethylmethylsulfonium bis(trifluoromethylsulfonyl)imide, [S 221 ][NTf 2 ], and triethylsulfonium bis(trifluoromethylsulfonyl)imide, [S 222 ][NTf 2 ]. 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.

  4. Ambient and laboratory observations of organic ammonium salts in PM1.

    Science.gov (United States)

    Schlag, P; Rubach, F; Mentel, T F; Reimer, D; Canonaco, F; Henzing, J S; Moerman, M; Otjes, R; Prévôt, A S H; Rohrer, F; Rosati, B; Tillmann, R; Weingartner, E; Kiendler-Scharr, A

    2017-08-24

    Ambient measurements of PM 1 aerosol chemical composition at Cabauw, the Netherlands, implicate higher ammonium concentrations than explained by the formation of inorganic ammonium salts. This additional particulate ammonium is called excess ammonium (e NH 4 ). Height profiles over the Cabauw Experimental Site for Atmospheric Research (CESAR) tower, of combined ground based and airborne aerosol mass spectrometric (AMS) measurements on a Zeppelin airship show higher concentrations of e NH 4 at higher altitudes compared to the ground. Through flights across the Netherlands, the Zeppelin based measurements furthermore substantiate e NH 4 as a regional phenomenon in the planetary boundary layer. The excess ammonium correlates with mass spectral signatures of (di-)carboxylic acids, making a heterogeneous acid-base reaction the likely process of NH 3 uptake. We show that this excess ammonium was neutralized by the organic fraction forming particulate organic ammonium salts. We discuss the significance of such organic ammonium salts for atmospheric aerosols and suggest that NH 3 emission control will have benefits for particulate matter control beyond the reduction of inorganic ammonium salts.

  5. Activation mechanism of ammonium ions on sulfidation of malachite (-201) surface by DFT study

    Science.gov (United States)

    Wu, Dandan; Mao, Yingbo; Deng, Jiushuai; Wen, Shuming

    2017-07-01

    The activation mechanism of ammonium ions on the sulfidation of malachite (-201) was determined by density functional theory (DFT) calculations. Results of DFT calculations indicated that interlayer sulfidation occurs during the sulfidation process of malachite (-201). The absorption of both the ammonium ion and sulfide ion on the malachite (-201) surface is stronger than that of sulfur ion. After sulfidation was activated with ammonium ion, the Cu 3d orbital peak is closer to the Fermi level and characterized by a stronger peak value. Therefore, the addition of ammonium ions activated the sulfidation of malachite (-201), thereby improving the flotation performance.

  6. The importance of ammonium mobility in nitrogen-impacted unfertilized grasslands: A critical reassessment

    International Nuclear Information System (INIS)

    Mian, Ishaq Ahmad; Riaz, Muhammad; Cresser, Malcolm S.

    2009-01-01

    The physico-chemical absorption characteristics of ammonium-N for 10 soils from 5 profiles in York, UK, show its high potential mobility in N deposition-impacted, unfertilized, permanent grassland soils. Substantial proportions of ammonium-N inputs were retained in the solution phase, indicating that ammonium translocation plays an important role in the N cycling in, and losses from, such soils. This conclusion was further supported by measuring the ammonium-N leaching from intact plant/soil microcosms. The ammonium-N absorption characteristics apparently varied with soil pH, depth and soil texture. It was concluded for the most acid soils especially that ammonium-N leached from litter horizons could be seriously limiting the capacity of underlying soils to retain ammonium. Contrary to common opinion, more attention therefore needs to be paid to ammonium leaching and its potential role in biogeochemical N cycling in semi-natural soil systems subject to atmospheric pollution. - Ammonium mobility is more important than previously thought in N-impacted, unfertilized grasslands

  7. Reduced blood flow increases the in vivo ammonium ion concentration in the RIF-1 tumor

    International Nuclear Information System (INIS)

    Constantinidis, Ioannis; Gamcsik, Michael P.

    1995-01-01

    Purpose: Previous studies from our laboratory have suggested that pooling of ammonium in tumor tissues may be caused by its inefficient removal due to the poor vasculature commonly found in tumors. The purpose of these experiments was to validate the relationship between tumor ammonium ion concentration and tumor blood flow, and to determine whether large concentrations of ammonium ion detected by Nuclear Magnetic Resonance (NMR) spectroscopy are either produced within the tumor or simply imported into the tumor through the blood stream. Methods and Materials: To test this hypothesis, we reduced blood flow in subcutaneously grown Radiation Induced Fibrosarcoma-1 (RIF-1) tumors, either by creating partial ischemia with a bolus injection of hydralazine or by occlusion with surgical sutures. 14 N and 31 P NMR spectroscopy were used to detect the presence of ammonium, and to assess the bioenergetic status of the tumors, respectively. Results: A correlation between ammonium ion concentration and (PCr(P i )) ratio was established for untreated tumors. An increase in the in vivo tumor ammonium ion concentration was observed for every tumor that experienced a reduction in blood flow caused by either hydralazine injection or suture ligation. Changes in ammonium ion concentration paralleled changes in the bioenergetics of hydralazine-treated tumors. Conclusion: Our results support the hypothesis that a reduction in tumor blood flow is responsible for the accumulation of ammonium in tumors, and that detected ammonium originated from within the tumor

  8. Titrimetric determination of uranium in tributyl phosphate

    International Nuclear Information System (INIS)

    Sobkowska, A.

    1978-01-01

    The titrimetric method involving the reduction of U(VI) to uranium(IV) by iron(II) in phosphoric acid, selective oxidation of the excess of iron(II) and potentiometric titration with dichromate was directly used for the determination of uranium in tributyl phosphate mixtures. The procedure was applied to solutions containing more than 2 mg of uranium in the sample but the highest precision and accuracy were obtained in the range from 20 to 200 mg of uranium. Dibutyl phosphate and monobutyl phosphate as well as the other radiolysis products of TBP had no influence on the results of determinations. (author)

  9. Uranium and heavy metals in phosphate fertilizers

    International Nuclear Information System (INIS)

    Khater, A.E.M.

    2008-01-01

    Agricultural applications of chemical fertilizers are a worldwide practice. The specific activity of uranium-238 and heavy metals in phosphate fertilizers depends on the phosphate ore from which the fertilizer produced and on the chemical processing of the ore. Composite phosphate fertilizers samples where collected and the uranium-238 specific activity, in Bq/kg, and As, Cd, Cu, Pb, Se concentration, in ppm, were measured. The annual addition of these elements in soil due to fertilization were calculated and discussed. (author)(tk)

  10. Global radiological impact of the phosphate fertilizers

    International Nuclear Information System (INIS)

    Morales, Rudnei Karam; Alves, Rex Nazare

    1996-01-01

    About ninety percent of the products obtained in the phosphate industry are directly used in agriculture as fertilizers. The uranium, thorium and radium content in phosphate fertilizers pollute the soil, water and air, creating risks due to associated natural radiation. This work shows the concentration of radionuclides present in various products of the national and American phosphate fertilizers industry, and compared them with worldwide mean values. The radiological impact of the products on the environment is evaluated and suggestions are presented in order to minimize the risks due to radioactivity. (author)

  11. Synthesis and Exfoliation of Discotic Zirconium Phosphates to Obtain Colloidal Liquid Crystals

    Science.gov (United States)

    Yu, Yi-Hsien; Wang, Xuezhen; Shinde, Abhijeet; Cheng, Zhengdong

    2016-01-01

    Due to their abundance in natural clay and potential applications in advanced materials, discotic nanoparticles are of interest to scientists and engineers. Growth of such anisotropic nanocrystals through a simple chemical method is a challenging task. In this study, we fabricate discotic nanodisks of zirconium phosphate [Zr(HPO4)2·H2O] as a model material using hydrothermal, reflux and microwave-assisted methods. Growth of crystals is controlled by duration time, temperature, and concentration of reacting species. The novelty of the adopted methods is that discotic crystals of size ranging from hundred nanometers to few micrometers can be obtained while keeping the polydispersity well within control. The layered discotic crystals are converted to monolayers by exfoliation with tetra-(n)-butyl ammonium hydroxide [(C4H9)4NOH, TBAOH]. Exfoliated disks show isotropic and nematic liquid crystal phases. Size and polydispersity of disk suspensions is highly important in deciding their phase behavior. PMID:27284765

  12. Sphingosine 1-phosphate and cancer.

    Science.gov (United States)

    Pyne, Nigel J; El Buri, Ashref; Adams, David R; Pyne, Susan

    2017-09-15

    The bioactive lipid, sphingosine 1-phosphate (S1P) is produced by phosphorylation of sphingosine and this is catalysed by two sphingosine kinase isoforms (SK1 and SK2). Here we discuss structural functional aspects of SK1 (which is a dimeric quaternary enzyme) that relate to coordinated coupling of membrane association with phosphorylation of Ser225 in the 'so-called' R-loop, catalytic activity and protein-protein interactions (e.g. TRAF2, PP2A and G q ). S1P formed by SK1 at the plasma-membrane is released from cells via S1P transporters to act on S1P receptors to promote tumorigenesis. We discuss here an additional novel mechanism that can operate between cancer cells and fibroblasts and which involves the release of the S1P receptor, S1P 2 in exosomes from breast cancer cells that regulates ERK-1/2 signalling in fibroblasts. This novel mechanism of signalling might provide an explanation for the role of S1P 2 in promoting metastasis of cancer cells and which is dependent on the micro-environmental niche. Copyright © 2017. Published by Elsevier Ltd.

  13. Radiation doses from phosphate fertilizers

    International Nuclear Information System (INIS)

    Anon.

    1975-01-01

    The activity concentrations determined of 226 Ra, 232 Th and 40 K in nCi/kg P 2 O 5 for the five most important kinds of fertilizer as well as their percent share in the economy year 1973/74 in the FRG are compiled in a table. From these values, the consumption of 0.917 million tons P 2 O 5 and from an average annual fertilizer coverage of 68.3 kg/ha, one can calculate a distribution of 32 Ci 226 Ra, 1 Ci 232 Th and 543 Ci 40 K over the total agriculturally used area, in other words, a deposit of 2.4 μCi 226 Ra, 0.07 μCi 232 Th and 40.5 μCi 40 K per ha. Taking a pessimistic view, an external radiation exposure of 0.11 mrad/a was calculated for gonads and bone marrow. If the total accumulation of 226 Ra (38% of the radiation exposure) from phosphate fertilizers from the ground during the last 80 years is assumed, then there is an exposure of 1.7 mrad/a for individual members of the population and 2.0 mrad/a for those occupied in agriculture. (HP/LH) [de

  14. Natural radioactivity in phosphate fertilizers

    International Nuclear Information System (INIS)

    Arndt, J.; Aurand, K.; Ruehle, H.; Schmier, H.; Wolter, R.

    1974-12-01

    The activity concentrations determined of 226 Ra, 232 Th and 40 K in nCi/kg P 2 O 5 for the five most important kinds of fertilizer as well as their percent share in the economy year 1973/74 in the FRG are compiled in a table. From these values, the consumption of 0.917 million tons P 2 O 5 and from an average annual fertilizer covering of 68.3 kg/ha, one can calculate a distribution of 32 Ci 226 Ra, 1 Ci 232 Th and 543 Ci 40 K over the total agriculturally used area, in other words a deposit of 2.4 μCi 226 Ra, 0.07 μCi 232 Th and 40.5 μCi 40 K per ha. Taking a pessimistic view, an external radiation exposure of 0.11 mrad/a was calculated for gonads and bone marrow. If the total accumulation of 226 Ra (38% of the radiation exposure) from phosphate fertilizers from the ground during the last 80 years is assumed, then there is an exposure of 1.7 mrad/a for individual members of the population and 2.0 mrad/a for those occupied in agriculture. (HP/LH) [de

  15. Removal of nitrate, ammonia and phosphate from aqueous solutions in packed bed filter using biochar augmented sand media

    Directory of Open Access Journals (Sweden)

    El Hanandeh Ali

    2017-01-01

    Full Text Available Nutrients from wastewater are a major source of pollution because they can cause significant impact on the ecosystem. Accordingly, it is important that the nutrient concentrations are kept to admissible levels to the receiving environment. Often regulatory limits are set on the maximum allowable concentrations in the effluent. Therefore, wastewater must be treated to meet safe levels of discharge. In this study, laboratory investigation of the efficiency of packed bed filters to remove nitrate, ammonium and phosphate from aqueous solutions were conducted. Sand and sand augmented with hydrochloric acid treated biochar (SBC were used as packing media. Synthetic wastewater solution was prepared with PO43−, NO3−, NH4+ concentrations 20, 10, 50 mg/L, respectively. Each experiment ran for a period of five days; samples from the effluent were collected on alternate days. All experiments were duplicated. Over the experiment period, the average removal efficiency of PO43−, NO3−, NH4+ were 99.2%, 72.9%, 96.7% in the sand packed columns and 99.2%, 82.3%, 97.4% in the SBC packed columns, respectively. Although, the presence of biochar in the packing media had little effect on phosphate and ammonium removal, it significantly improved nitrate removal.

  16. Phosphate solubilization and acid phosphatase activity of Serratia sp. isolated from mangrove soil of Mahanadi river delta, Odisha, India

    Directory of Open Access Journals (Sweden)

    B.C. Behera

    2017-06-01

    Full Text Available Phosphorus is an essential element for all life forms. Phosphate solubilizing bacteria are capable of converting phosphate into a bioavailable form through solubilization and mineralization processes. Hence in the present study a phosphate solubilizing bacterium, PSB-37, was isolated from mangrove soil of the Mahanadi river delta using NBRIP-agar and NBRIP-BPB broth containing tricalcium phosphate as the phosphate source. Based on phenotypic and molecular characterization, the strain was identified as Serratia sp. The maximum phosphate solubilizing activity of the strain was determined to be 44.84 μg/ml, accompanied by a decrease in pH of the growth medium from 7.0 to 3.15. During phosphate solubilization, various organic acids, such as malic acid (237 mg/l, lactic acid (599.5 mg/l and acetic acid (5.0 mg/l were also detected in the broth culture through HPLC analysis. Acid phosphatase activity was determined by performing p-nitrophenyl phosphate assay (pNPP of the bacterial broth culture. Optimum acid phosphatase activity was observed at 48 h of incubation (76.808 U/ml, temperature of 45 °C (77.87 U/ml, an agitation rate of 100 rpm (80.40 U/ml, pH 5.0 (80.66 U/ml and with glucose as a original carbon source (80.6 U/ml and ammonium sulphate as a original nitrogen source (80.92 U/ml. Characterization of the partially purified acid phosphatase showed maximum activity at pH 5.0 (85.6 U/ml, temperature of 45 °C (97.87 U/ml and substrate concentration of 2.5 mg/ml (92.7 U/ml. Hence the present phosphate solubilizing and acid phosphatase production activity of the bacterium may have probable use for future industrial, agricultural and biotechnological application.

  17. Hemodialysis for near-fatal sodium phosphate toxicity in a child receiving sodium phosphate enemas.

    Science.gov (United States)

    Becknell, Brian; Smoyer, William E; O'Brien, Nicole F

    2014-11-01

    This study aimed to demonstrate the importance of considering hemodialysis as a treatment option in the management of sodium phosphate toxicity. This is a case report of a 4-year-old who presented to the emergency department with shock, decreased mental status, seizures, and tetany due to sodium phosphate toxicity from sodium phosphate enemas. Traditional management of hyperphosphatemia with aggressive hydration and diuretics was insufficient to reverse the hemodynamic and neurological abnormalities in this child. This is the first report of the use of hemodialysis in a child without preexisting renal failure for the successful management of near-fatal sodium phosphate toxicity. Hemodialysis can safely be used as an adjunctive therapy in sodium phosphate toxicity to rapidly reduce serum phosphate levels and increase serum calcium levels in children not responding to conventional management.

  18. Performance of pineapple slips inoculated with diazotrophic phosphate-solubilizing bacteria and rock phosphate

    OpenAIRE

    Lílian Estrela Borges Baldotto; Marihus Altoé Baldotto; Fábio Lopes Olivares; Adriane Nunes de Souza

    2014-01-01

    Besides fixing N2, some diazotrophic bacteria or diazotrophs, also synthesize organic acids and are able to solubilize rock phosphates, increasing the availability of P for plants. The application of these bacteria to pineapple leaf axils in combination with rock phosphate could increase N and P availability for the crop, due to the bacterial activity of biological nitrogen fixation and phosphate solubilization. The objectives of this study were: (i) to select and characterize diazotrophs abl...

  19. Uranium recovery from phosphate rocks concentrated

    International Nuclear Information System (INIS)

    Azevedo, M.F. de.

    1986-01-01

    The reserves, geological data, chemical data and technical flowsheet from COPEBRAS and Goiasfertil ores are described, including the process of mining ore concentration. Samples of Goiasfertil ores are analysed by gravimetric analysis, for phosphate, and spectrofluorimetry for uranium. (author)

  20. Hanford phosphate precipitation filtration process evaluation

    International Nuclear Information System (INIS)

    Walker, B.W.; McCabe, D.J.

    1997-01-01

    The purpose of this filter study was to evaluate cross-flow filtration as effective solid-liquid separation technology for treating Hanford wastes, outline operating conditions for equipment, examine the expected filter flow rates, and determine proper cleaning. A proposed Hanford waste pre-treatment process uses sodium hydroxide at high temperature to remove aluminum from sludge. This process also dissolves phosphates. Upon cooling to 40 degrees centigrade the phosphates form a Na7(PO4)2F9H2O precipitate which must be removed prior to further treatment. Filter studies were conducted with a phosphate slurry simulant to evaluate whether 0.5 micron cross-flow sintered metal Mott filters can separate the phosphate precipitate from the wash solutions. The simulant was recirculated through the filters at room temperature and filtration performance data was collected

  1. short communication agronomic effectiveness of novel phosphate

    African Journals Online (AJOL)

    igneous Dorowa (Zimbabwe) phosphate rock was investigated in a greenhouse ... are higher than the levels considered desirable for acidulation was selected based on proportions ... The analysis for dry matter yield of and P uptake by maize ...

  2. Phosphate coating on stainless steel 304 sensitized

    International Nuclear Information System (INIS)

    Cruz V, J. P.; Vite T, J.; Castillo S, M.; Vite T, M.

    2009-01-01

    The stainless steel 304 can be sensitized when welding processes are applied, that causes the precipitation of chromium carbide in the grain limits, being promoted in this way the formation of galvanic cells and consequently the corrosion process. Using a phosphate coating is possible to retard the physiochemical damages that can to happen in the corrosion process. The stainless steel 304 substrate sensitized it is phosphate to base of Zn-Mn, in a immersion cell very hot. During the process was considered optimization values, for the characterization equipment of X-rays diffraction and scanning electron microscopy was used. The XRD technique confirmed the presence of the phases of manganese phosphate, zinc phosphate, as well as the phase of the stainless steel 304. When increasing the temperature from 60 to 90 C in the immersion process a homogeneous coating is obtained. (Author)

  3. Issues of natural radioactivity in phosphates

    International Nuclear Information System (INIS)

    Schnug, E.; Haneklaus, S.; Schnier, C.; Scholten, L.C.

    1996-01-01

    The fertilization of phosphorus (P) fertilizers is essential in agricultural production, but phosphates contain in dependence on their origin different amounts of trace elements. The problem of cadmium (Cd) loads and other heavy metals is well known. However, only a limited number of investigations examined the contamination of phosphates with the two heaviest metals, uranium (U) and thorium (Th), which are radioactive. Also potassium (K) is lightly radioactive. Measurements are done n the radioactivity content of phosphates, P fertilizers and soils. The radiation doses to workers and public as well as possible contamination of soils from phosphate rock or fertilizer caused by these elements or their daughter products is of interest with regard to radiation protection. The use of P fertilizers is necessary for a sustainable agriculture, but it involves radioactive contamination of soils. The consequences of the use of P fertilizers is discussed, also with regard to existing and proposed legislation. 11 refs., 2 figs., 7 tabs

  4. Geochemistry and mineralogy of Ogun phosphate rock

    African Journals Online (AJOL)

    user

    m deep) within the same location. The pellets ... diffracted rays are collected by a detector and the information relayed to a ... Ogun phosphate deposits were formed in shallow marine ... process thus confirming the earlier work done by Jones.

  5. Rock phosphate solubilization by the ectomycorrhizal fungus ...

    African Journals Online (AJOL)

    SAM

    2014-06-18

    Jun 18, 2014 ... phosphate solubilization is accompanied by acid production. Thus, the evidence ..... of organic acids. (Khan et al., 2010) such as acetate, lactate, oxalate, ... (2014) also observed that oxalic acid was secreted by L. fraterna to ...

  6. Thermal stability of phosphate coatings on steel

    Czech Academy of Sciences Publication Activity Database

    Pokorný, P.; Szelag, P.; Novák, M.; Mastný, L.; Brožek, Vlastimil

    2015-01-01

    Roč. 54, č. 3 (2015), s. 489-492 ISSN 0543-5846 Institutional support: RVO:61389021 Keywords : Steel * phosphates * coatings * structure Subject RIV: CA - Inorganic Chemistry Impact factor: 0.959, year: 2014

  7. Corrosion inhibition by lithium zinc phosphate pigment

    International Nuclear Information System (INIS)

    Alibakhshi, E.; Ghasemi, E.; Mahdavian, M.

    2013-01-01

    Highlights: •Synthesis of lithium zinc phosphate (LZP) by chemical co-precipitation method. •Corrosion inhibition activity of pigments compare with zinc phosphate (ZP). •LZP showed superior corrosion inhibition effect in EIS measurements. •Evaluation of adhesion strength and dispersion stability. -- Abstract: Lithium zinc phosphate (LZP) has been synthesized through a co-precipitation process and characterized by XRD and IR spectroscopy. The inhibitive performances of this pigment for corrosion of mild steel have been discussed in comparison with the zinc phosphate (ZP) in the pigment extract solution by means of EIS and in the epoxy coating by means of salt spray. The EIS and salt spray results revealed the superior corrosion inhibitive effect of LZP compared to ZP. Moreover, adhesion strength and dispersion stability of the pigmented epoxy coating showed the advantage of LZP compared to ZP

  8. A new crystal modification of diammonium hydrogen phosphate, (NH42(HPO4

    Directory of Open Access Journals (Sweden)

    Bernhard Spingler

    2010-04-01

    Full Text Available The addition of hexafluoridophosphate salts (ammonium, silver, thallium or potassium is usually used to precipitate complex cations from aqueous solutions. It has long been known that PF6− is sensitive towards hydrolysis under acidic conditions [Gebala & Jones (1969. J. Inorg. Nucl. Chem. 31, 771–776; Plakhotnyk et al. (2005. J. Fluorine Chem. 126, 27–31]. During the course of our investigation into coinage metal complexes of diphosphine ligands, we used ammonium hexafluoridophosphate in order to crystallize [Ag(diphosphine2]PF6 complexes. From these solutions we always obtained needle-like crystals which turned out to be the title compound, 2NH4+·HPO42−. It was received as the hydrolysis product of NH4PF6. The crystals are a new modification of diammonium hydrogen phosphate. In contrast to the previously published polymorph [Khan et al. (1972. Acta Cryst. B28, 2065–2069], Z′ of the title compound is 2. In the new modification of the title compound, there are eight molecules of (NH42(HPO4 in the unit cell. The structure consists of PO3OH and NH4 tetrahedra, held together by O—H...O and N—H...O hydrogen bonds.

  9. Assessment of the potential for ammonium nitrate formation and reaction in Tank 241-SY-101

    International Nuclear Information System (INIS)

    Pederson, L.R.; Bryan, S.A.

    1994-08-01

    Two principal scenarios by which ammonium nitrate may be formed were considered: (a) precipitation of ammonium nitrate in the waste, and (b) ammonium nitrate formation via the gas phase reaction of ammonia and nitrogen dioxide. The first of these can be dismissed because ammonium ions, which are necessary for ammonium nitrate precipitation, can exist only in negligibly small concentrations in strongly alkaline solutions. Gas phase reactions between ammonia, nitrogen dioxide, and water vapor in the gas phase represent the most likely means by which ammonium nitrate aerosols could be formed in Tank 241-SY-101. Predicted ammonium nitrate formation rates are largely controlled by the concentration of nitrogen dioxide. This gas has not been detected among those gases vented from the wastes using Fourier Transform Infrared Spectrometry (FTIR) or mass spectrometry. While detection limits for nitrogen dioxide have not been established experimentally, the maximum concentration of nitrogen dioxide in the gas phase in Tank 241-SY-101 was estimated at 0.1 ppm based on calculations using the HITRAN data base and on FTIR spectra of gases vented from the wastes. At 50 C and with 100 ppm ammonia also present, less than one gram of ammonium nitrate per year is estimated to be formed in the tank. To date, ammonium nitrate has not been detected on HEPA filters in the ventilation system, so any quantity that has been formed in the tank must be quite small, in good agreement with rate calculations. The potential for runaway exothermic reactions involving ammonium nitrate in Tank 241-SY-101 is minimal. Dilution by non-reacting waste components, particularly water, would prevent hazardous exothermic reactions from occurring within the waste slurry, even if ammonium nitrate were present. 41 refs

  10. Synthesis and characterization of porous calcium phosphate

    International Nuclear Information System (INIS)

    Granados C, F.; Serrano G, J.; Bonifacio M, J.

    2007-01-01

    The porous calcium phosphate was prepared by the continuous precipitation method using Ca(NO 3 ) 2 .4H 2 O and NH 4 H 2 PO 4 salts. The synthesized material was structurally and superficially characterized using the XRD, BET, IR TGA and SEM techniques. The obtained inorganic material was identified as calcium phosphate that presents a great specific area for what can be efficiently used as adsorbent material for adsorption studies in the radioactive wastes treatment present in aqueous solution. (Author)

  11. Removal of organic wastes containing tributyl phosphate

    International Nuclear Information System (INIS)

    Drobnik, S.

    TBP in dodecane and kerosene is one of the waste solutions from the reprocessing of spent nuclear fuels by the Purex process. The following methods were investigated for removing the organic solvents: adsorption on suitable solids, extraction, reaction with neutral salts, and saponification with acids or alkalis. Results showed that the best method of TBP removal is saponification with alkali hydroxides, either with dibutyl phosphate or with ortho-phosphate

  12. Kinetics of strontium sorption in calcium phosphate

    International Nuclear Information System (INIS)

    Bacic, S.; Komarov, V.F.; Vukovic, Z.

    1989-01-01

    Kinetics of strontium sorption by highly dispersed solids: tricalcium phosphate (Ca 3 (PO 4 ) 2 , TCP) and hydroxyapatite (Ca 5 (PO 4 ) 3 )H, HAP) were investigated. Analysis of sorption data was made taking into consideration composition and morphology of ultra micro particles. Conclusion is that the isomorphous strontium impurity is structurally sensitive element for calcium phosphate. It was determined that the beginning of strontium desorption corresponds to the beginning of transformation of the TCP - HAP (author)

  13. Phosphate transporter mediated lipid accumulation in Saccharomyces cerevisiae under phosphate starvation conditions.

    Science.gov (United States)

    James, Antoni W; Nachiappan, Vasanthi

    2014-01-01

    In the current study, when phosphate transporters pho88 and pho86 were knocked out they resulted in significant accumulation (84% and 43%) of triacylglycerol (TAG) during phosphate starvation. However in the presence of phosphate, TAG accumulation was only around 45% in both pho88 and pho86 mutant cells. These observations were confirmed by radio-labeling, fluorescent microscope and RT-PCR studies. The TAG synthesizing genes encoding for acyltransferases namely LRO1 and DGA1 were up regulated. This is the first report for accumulation of TAG in pho88Δ and pho86Δ cells under phosphate starvation conditions. Copyright © 2013. Published by Elsevier Ltd.

  14. Studies on effective decomposition of monazite minerals by variety of phosphate fluxes for simple and direct determination of uranium by LED fluorimeter

    International Nuclear Information System (INIS)

    Gopal, Leela; Hanuman, V.V.; Chakrapani, G.

    2013-01-01

    A simple, rapid, effective sample decomposition method is developed for the determination of uranium (U) in monazite minerals by fluorimetric (Light Emitting Diodes (LED) based) technique. The salts of sodium dihydrogen phosphate (NaH 2 PO 4 ), disodium hydrogen phosphate (Na 2 HPO 4 ) and tetrasodium pyrophosphate (Na 4 P 2 O 7 ) were used to conduct studies on effective decomposition and dissolution of monazite minerals. The flux short listed for sample decomposition has several advantages. The fusion is very simple (involve minimal skills), time saving and eco-friendly (no acids were used for sample dissolution), where as in the reported conventional sample decomposition methods involving fusion with sodium peroxide, mixture of KHF 2 and NaF, mineral acids are being used for sample decomposition to get clear solution. Further this solution cannot be used directly for uranium determination by LED fluorimetry; hence separation is required, resulting in low sample throughput. In the present method no such separation is required as the flux itself acts as a fluorescence enhancing reagent and buffer (maintaining the optimum pH of 7.1 ± 0.1). The fused melt of the flux mixture when dissolved in water, gives clear and stable solution. The accuracy and precision of the method was evaluated by analyzing Certified Reference Material, IGS-36 (Institute of Geological Sciences, UK) and monazite samples received from BSOI, Trivandrum. The accuracy of the data was further evaluated by comparing with conventional standard decomposition methods. The results are well within experimental error. RSD of the method is ±2% at 0.30% U 3 O 8 in monazite minerals. (author)

  15. Phosphate rock costs, prices and resources interaction.

    Science.gov (United States)

    Mew, M C

    2016-01-15

    This article gives the author's views and opinions as someone who has spent his working life analyzing the international phosphate sector as an independent consultant. His career spanned two price hike events in the mid-1970's and in 2008, both of which sparked considerable popular and academic interest concerning adequacy of phosphate rock resources, the impact of rising mining costs and the ability of mankind to feed future populations. An analysis of phosphate rock production costs derived from two major industry studies performed in 1983 and 2013 shows that in nominal terms, global average cash production costs increased by 27% to $38 per tonne fob mine in the 30 year period. In real terms, the global average cost of production has fallen. Despite the lack of upward pressure from increasing costs, phosphate rock market prices have shown two major spikes in the 30 years to 2013, with periods of less volatility in between. These price spike events can be seen to be related to the escalating investment cost required by new mine capacity, and as such can be expected to be repeated in future. As such, phosphate rock price volatility is likely to have more impact on food prices than rising phosphate rock production costs. However, as mining costs rise, recycling of P will also become increasingly driven by economics rather than legislation. Copyright © 2015 Elsevier B.V. All rights reserved.

  16. Sphingosine 1-Phosphate and Atherosclerosis

    Science.gov (United States)

    Yatomi, Yutaka

    2018-01-01

    Sphingosine 1-phosphate (S1P) is a potent lipid mediator that works on five kinds of S1P receptors located on the cell membrane. In the circulation, S1P is distributed to HDL, followed by albumin. Since S1P and HDL share several bioactivities, S1P is believed to be responsible for the pleiotropic effects of HDL. Plasma S1P levels are reportedly lower in subjects with coronary artery disease, suggesting that S1P might be deeply involved in the pathogenesis of atherosclerosis. In basic experiments, however, S1P appears to possess both pro-atherosclerotic and anti-atherosclerotic properties; for example, S1P possesses anti-apoptosis, anti-inflammation, and vaso-relaxation properties and maintains the barrier function of endothelial cells, while S1P also promotes the egress and activation of lymphocytes and exhibits pro-thrombotic properties. Recently, the mechanism for the biased distribution of S1P on HDL has been elucidated; apolipoprotein M (apoM) carries S1P on HDL. ApoM is also a modulator of S1P, and the metabolism of apoM-containing lipoproteins largely affects the plasma S1P level. Moreover, apoM modulates the biological properties of S1P. S1P bound to albumin exerts both beneficial and harmful effects in the pathogenesis of atherosclerosis, while S1P bound to apoM strengthens anti-atherosclerotic properties and might weaken the pro-atherosclerotic properties of S1P. Although the detailed mechanisms remain to be elucidated, apoM and S1P might be novel targets for the alleviation of atherosclerotic diseases in the future. PMID:28724841

  17. Summary of safety evaluation toxicity studies of glufosinate ammonium.

    Science.gov (United States)

    Ebert, E; Leist, K H; Mayer, D

    1990-05-01

    This article reviews the results of toxicity studies to evaluate the safety of the herbicide glufosinate ammonium (GLA) and its formulation (200 g/litre) in laboratory animals. The data show that GLA and its formulation are slightly toxic following oral exposure. In addition, the formulation induced GLA and its formulation are slightly toxic following oral exposure. In addition, the formulation induced slight dermal toxicity and eye irritation. Testing for teratogenicity in rats and rabbits indicated no teratogenic potential, and numerous mutagenicity tests showed GLA to be non-genotoxic. Chronic toxicity testing in rats and dogs yielded no-observable-effect levels of 2 and 5 mg/kg body weight/day, respectively. Oncogenicity studies in rats and mice revealed no carcinogenic potential. On the basis of these toxicity data it is concluded that this herbicide is safe under conditions of recommended use.

  18. Reversible Splenial Lesion Syndrome (RESLES) Following Glufosinate Ammonium Poisoning.

    Science.gov (United States)

    Jeong, Tae Oh; Yoon, Jae Chol; Lee, Jae Baek; Jin, Young Ho; Hwang, Seung Bae

    2015-01-01

    Isolated and reversible lesion restricted to the splenium of the corpus callosum, known as reversible splenial lesion syndrome, have been reported in patients with infection, high-altitude cerebral edema, seizures, antiepileptic drug withdrawal, or metabolic disturbances. Here, we report a 39-year-old female patient with glufosinate ammonium (GLA) poisoning who presented with confusion and amnesia. Diffusion-weighted magnetic resonance imaging of the brain revealed cytotoxic edema of the splenium of the corpus callosum. The lesion was not present on follow-up MR imaging performed 9 months later. We postulate that a GLA-induced excitotoxic mechanism was the cause of this reversible splenial lesion. Copyright © 2015 by the American Society of Neuroimaging.

  19. Functionalizing aluminum substrata by quaternary ammonium for antifouling performances

    Science.gov (United States)

    He, Xiaoyan; Suo, Xinkun; Bai, Xiuqin; Yuan, Chengqing; Li, Hua

    2018-05-01

    Due to the great loss induced by biofouling, developing new strategies for combating biofouling has attracted extensive attention. Quaternary ammonium salts are potent cationic antimicrobials used in consumer products and their use for surface immobilization could create a contact-active antimicrobial layer. Here we report the facile preparation of a contact-active antifouling coating by tethering polyethyleneimine (PEI) onto flat/nanostructured aluminum surface by hydrogen bonding between PEI and AlOOH. Quaternized PEI (QPEI) is obtained through quaternization reactions. Biofouling testing suggests excellent antifouling performances of the samples by declining the adhesion of 95% Phaeodactylum tricornutum and 98% of Chlorella pyrenoidosa. The antifouling properties of PEI/QPEI are attributed predominately to their hydrophilic and antimicrobial nature. The technical route of PEI/QPEI surface grafting shows great potential for modifying marine infrastructures for enhanced antifouling performances.

  20. Integrated Data Collection Analysis (IDCA) Program — Ammonium Nitrate

    Energy Technology Data Exchange (ETDEWEB)

    Sandstrom, Mary M. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Brown, Geoffrey W. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Preston, Daniel N. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Pollard, Colin J. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Warner, Kirstin F. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States). Indian Head Division; Sorensen, Daniel N. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States). Indian Head Division; Remmers, Daniel L. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States). Indian Head Division; Phillips, Jason J. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Shelley, Timothy J. [Bureau of Alcohol, Tobacco and Firearms, Redstone Arsenal, AL (United States); Reyes, Jose A. [Applied Research Associates, Tyndall AFB, FL (United States); Hsu, Peter C. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Reynolds, John G. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    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.

  1. Computational Modeling of Degradation of Substituted Benzyltrimethyl Ammonium: Preprint

    Energy Technology Data Exchange (ETDEWEB)

    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.

  2. Removal of oil palm trunk lignin in ammonium hydroxide pretreatment

    Science.gov (United States)

    Az-Zahraa, Balqis; Zakaria, Sarani; Daud, Muhammad F. B.; Jaafar, Sharifah Nabihah Syed

    2018-04-01

    Alkaline pretreatment using ammonium hydroxide, NH4OH serves as one of a process to remove lignin from lignocellulosic biomass such as oil palm trunk fiber. In this study, the effect of NH4OH pretreatment on removal of oil palm trunk lignin was investigated. The oil palm trunk fiber was dissolved in NH4OH with different concentrations (6, 8 and 10 %), different duration (3, 5 and 7 h) and temperatures (60, 80 and 100 °C). The samples were analyzed by using UV-Vis to estimate the concentration of extracted lignin. The result indicates that the optimum conditions to gain maximum extracted lignin were 8% NH4OH, 100 °C and 5 h with concentration of 64 mgL-1 while the lowest was at 6% NH4OH, 100 °C and 5 h with concentration of 62.5 mgL-1.

  3. Engineering application of anaerobic ammonium oxidation process in wastewater treatment.

    Science.gov (United States)

    Mao, Nianjia; Ren, Hongqiang; Geng, Jinju; Ding, Lili; Xu, Ke

    2017-08-01

    Anaerobic ammonium oxidation (Anammox), a promising biological nitrogen removal process, has been verified as an efficient, sustainable and cost-effective alternative to conventional nitrification and denitrification processes. To date, more than 110 full-scale anammox plants have been installed and are in operation, treating industrial NH 4 + -rich wastewater worldwide, and anammox-based technologies are flourishing. This review the current state of the art for engineering applications of the anammox process, including various anammox-based technologies, reactor selection and attempts to apply it at different wastewater plants. Process control and implementation for stable performance are discussed as well as some remaining issues concerning engineering application are exposed, including the start-up period, process disturbances, greenhouse gas emissions and especially mainstream anammox applications. Finally, further development of the anammox engineering application is proposed in this review.

  4. Antibacterial effect of composite resins containing quaternary ammonium polyethyleneimine nanoparticles

    International Nuclear Information System (INIS)

    Yudovin-Farber, Ira; Beyth, Nurit; Weiss, Ervin I.; Domb, Abraham J.

    2010-01-01

    Quaternary ammonium polyethyleneimine (QA-PEI)-based nanoparticles were synthesized by crosslinking with dibromopentane followed by N-alkylation with various alkyl halides and further N-methylation with methyl iodide. Insoluble pyridinium-type particles were prepared by suspension polymerization of 4-vinyl pyridine followed by N-alkylation with alkyl halides. Polyamine-based nanoparticles embedded in restorative composite resin at 1% w/w were tested for antibacterial activity against Streptococcus mutans using direct contact test. Activity analysis revealed that the alkyl chain length of the QA-PEI nanoparticles plays a significant role in antibacterial activity of the reagent. The most potent compound was octyl-alkylated QA-PEI embedded in restorative composite resin at 1% w/w that totally inhibited S. mutans growth in 3-month-aged samples. This data indicates that restorative composite resin with antibacterial properties can be produced by the incorporation of QA-PEI nanoparticles.

  5. Antibacterial effect of composite resins containing quaternary ammonium polyethyleneimine nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Yudovin-Farber, Ira [Hebrew University of Jerusalem, Department of Medicinal Chemistry and Natural Products, School of Pharmacy, Faculty of Medicine (Israel); Beyth, Nurit; Weiss, Ervin I. [Hebrew University of Jerusalem, Department of Prosthodontics, Faculty of Dentistry (Israel); Domb, Abraham J., E-mail: avid@ekmd.huji.ac.i [Hebrew University of Jerusalem, Department of Medicinal Chemistry and Natural Products, School of Pharmacy, Faculty of Medicine (Israel)

    2010-02-15

    Quaternary ammonium polyethyleneimine (QA-PEI)-based nanoparticles were synthesized by crosslinking with dibromopentane followed by N-alkylation with various alkyl halides and further N-methylation with methyl iodide. Insoluble pyridinium-type particles were prepared by suspension polymerization of 4-vinyl pyridine followed by N-alkylation with alkyl halides. Polyamine-based nanoparticles embedded in restorative composite resin at 1% w/w were tested for antibacterial activity against Streptococcus mutans using direct contact test. Activity analysis revealed that the alkyl chain length of the QA-PEI nanoparticles plays a significant role in antibacterial activity of the reagent. The most potent compound was octyl-alkylated QA-PEI embedded in restorative composite resin at 1% w/w that totally inhibited S. mutans growth in 3-month-aged samples. This data indicates that restorative composite resin with antibacterial properties can be produced by the incorporation of QA-PEI nanoparticles.

  6. Thermophysical properties of two ammonium-based protic ionic liquids

    Science.gov (United States)

    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

  7. Spectrophotometric determination of boron in ammonium diuranate and interference studies

    International Nuclear Information System (INIS)

    Ramanjaneyulu, P.S.; Raman, V.A.; Sayi, Y.S.; Ramakumar, K.L.

    2005-01-01

    This paper describes determination of boron in ammonium diuranate by spectrophotometry employing curcumin as a complexing agent after extraction of boron with 2-ethyl hexane 1,3 diol. Two diluents namely ethyl alcohol (EtOH) and N,N-dimethyl formamide (DMF) were investigated for the preparation of final solution. It was observed that the blank is less with DMF presumably due to higher extent of deprotonation of uncomplexed curcumin. The detection limits of method for 25 and 10 ml dilution are 20 ng and 10 ng respectively. Interference studies for several cation and anion species like Al, Cr, Mg, Ca, Fe, Mn, Mo, F, W, NO, and different amount of 10% EHD in CHCl 3 are also discussed. (author)

  8. Ammonium Laurate Surfactant for Cleaner Deposition of Carbon Nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Nilsson, Hanna M. [Department of Material Science and Engineering and ‡Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, United States; Meany, Brendan [Department of Material Science and Engineering and ‡Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, United States; Ticey, Jeremy [Department of Material Science and Engineering and ‡Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, United States; Sun, Chuan-Fu [Department of Material Science and Engineering and ‡Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, United States; Wang, YuHuang [Department of Material Science and Engineering and ‡Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, United States; Cumings, John [Department of Material Science and Engineering and ‡Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, United States

    2015-06-15

    Experiments probing the properties of individual carbon nanotubes (CNTs) and those measuring bulk composites show vastly different results. One major issue limiting the results is that the procedures required to separate and test CNTs introduce contamination that changes the properties of the CNT. These contamination residues often come from the resist used in lithographic processing and the surfactant used to suspend and deposit the CNTs, commonly sodium dodecyl sulfate (SDS). Here we present ammonium laurate (AL), a surfactant that has previously not been used for this application, which differs from SDS only by substitution of ionic constituents but shows vastly cleaner depositions. In addition, we show that compared to SDS, AL-suspended CNTs have greater shelf stability and more selective dispersion. These results are verified using transmission electron microscopy, atomic force microscopy, ζ-potential measurements, and Raman and absorption optical spectroscopy. This surfactant is simple to prepare, and the nanotube solutions require minimal sonication and centrifugation in order to outperform SDS.

  9. Non-ammonium reduced nitrogen species in atmospheric aerosol particles

    Energy Technology Data Exchange (ETDEWEB)

    Dod, R.L.; Gundel, L.A.; Benner, W.H.; Novakov, T.

    1983-08-01

    The traditional belief that ambient aerosol particles contain nitrogen predominantly in the form of inorganic ionic species such as NH/sub 4//sup +/ and NO/sub 3//sup -/ was challenged about 10 years ago by results from x-ray photoelectron spectroscopic analysis (ESCA) of California aerosol particles. A significant fraction (approx. 50%) of the reduced nitrogen was observed to have an oxidation state more reduced than ammonium, characteristic of organic nitrogen species. We have used a recently developed thermal evolved gas analysis method (NO/sub x/) in conjunction with ESCA to confirm the existence of these species in aerosol particles collected in both the United States and Europe. The agreement of EGA and ESCA analyses indicates that these species are found not only on the surface but also throughout the particles. 9 references, 6 figures.

  10. Review of Options for Ammonia/Ammonium Management

    Energy Technology Data Exchange (ETDEWEB)

    Nash, C. A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2016-05-06

    This report is a review of literature supporting practical ammonia/ammonium destruction processes. Melter research supporting Hanford Low Activity Waste (LAW) glass production has shown that significant amounts of ammonia will be in the melter offgas condensate. Further work with secondary waste forms indicates the potential need to remove the ammonia, perhaps by an oxidative process. This review finds likely practical chemical methods to oxidize ammonia in aqueous solution at moderate temperatures and atmospheric pressure, using easily obtained reagents. Leading candidates include nitrite oxidation to produce nitrogen gas, various peroxide oxidative processes, and air stripping. This work reviews many other processes and provides reasoning to not consider those processes further for this application.

  11. Thermophysical properties of two ammonium-based protic ionic liquids.

    Science.gov (United States)

    Bhattacharjee, Arijit; Coutinho, João A P; Freire, Mara G; Carvalho, Pedro J

    2015-04-01

    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, [N 11{2(N11)}H ][CH 3 CO 2 ], and N-ethyl-N,N-dimethylammonium phenylacetate, [N 112H ][C 7 H 7 CO 2 ]. 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.

  12. The Ability of Watercress (Nasturtiumofficinale and Pennyroyal (Menthapulegium in Clean up Excess Nitrate and Phosphate of Water

    Directory of Open Access Journals (Sweden)

    Z. Ahmadpoor

    2016-02-01

    Full Text Available Introduction: There is necessary to clean up the nitrate and phosphate from surface waters before effluence of them to environment and eutrophication formation because of water health importance and considering to nitrate and phosphate consequences. Nitrate and ammonium as the - forms of inorganic and nitrogen have been subjected to the center of issues related to environment pollutants and water resources in a long time. The nitrate is more important than other inorganic nitrogen forms such as ammonium because of various reasons such as high dynamics and causing diseases such as some of digestion system and lymph nodes cancers in adults and methemoglobinemia in infants. Therefore the maximum concentration of this ion in drinking water has been determined as 45 mg.Lit-1 by WHO. Regarding the importance of the water health and the complications due to existence of some compounds such as nitrate and phosphate, in this experiment, the possibility of elimination or decreasing excess nitrate and phosphate from water in hydroponic conditions using of two watercress and pennyroyal plants was evaluated. Watercress(Nasturtiumofficinale and pennyroyal (Menthapulegiumwere selected because of some properties such as adaptability with the most climates of Iranamd less requirements care. Materials and Methods: Two RCD factorial experiments were carried out to evaluate the ability of watercress and pennyroyal to biosorption of nitrate and phosphate from polluted water in hydroponic conditions. First factor was plant species including watercress and pennyroyal. Second factor included nitrate (50, 100, 150 Mg/L and phosphate (5, 10, 15 Mg/L in first and second experiment respectively.The final concentrations of nitrate and phosphate in water was measured using spectrophotometer in wavelength of 410 nm and 690 nm by sulphatebrucine and chloride methods , respectively, which are mentioned in Standard Methods for the Examination of Water and Wastewater. At the end

  13. Facile synthesis of ammonium vanadate nanofibers by using reflux in aqueous V{sub 2}O{sub 5} solution with ammonium persulfate

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Se Hun [Department of Convergence Nanoscience, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Koo, Jun Mo [Department of Organic and Nano Engineering, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Oh, Seong Geun, E-mail: seongoh@hanyang.ac.kr [Department of Chemical Engineering, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Im, Seung Soon, E-mail: imss007@hanyang.ac.kr [Department of Convergence Nanoscience, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Department of Organic and Nano Engineering, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul 133-791 (Korea, Republic of)

    2017-06-15

    Ammonium vanadate nanofibers were synthesized by simple reflux method in aqueous V{sub 2}O{sub 5} solution with ammonium persulfate without relying on surfactants, catalysts, harmful solvents and autoclave. The degree of intercalation by cationic ammonium ions into the crystal structure of vanadium oxide along with its change in chemical composition were analyzed by thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), infrared spectroscopy (IR). The morphological changes toward nanofiber structure, having diameter of 20–30 nm and a few μm length, were investigated using transmission electron microscopy (TEM), scanning electron microscopy (SEM) and X-ray diffraction (XRD). The influences of synthetic conditions, such as reaction time and concentration of sulfate (SO{sub 4}{sup 2-}), on the crystal structures and morphologies of the resulting products have investigated. As a result, the ammonium vanadate nanofiber was formed in a short reaction time through a simple reflux method and yielded comparable electrical conductivity 1.47 × 10{sup -2} S/cm. - Highlights: • Ammonium vanadate nanofiber (AVFr) was prepared by simple reflux method. • AVFr yielded comparable electrical conductivity 1.47 × 10{sup -2} S/cm. • The electrical conductivity was improved by the increased amount of ammonium ion. • Sulfate ions (SO{sub 4}{sup 2-}) play a crucial role in controlling the morphology of nanofiber.

  14. The production of sinterable uranium dioxide from ammonium diuranate

    International Nuclear Information System (INIS)

    Fane, A.G.; Le Page, A.H.

    1975-02-01

    The development of a 0.13 m diameter pulsed fluidised bed reactor for the continuous production of sinterable uranium dioxide from ammonium diuranate is described. Calcination-reduction at 670 to 680 0 C produced powders with surface areas of 4 to 6 m 2 g -1 giving pellet densities in excess of 10.6 g cm -3 . Sinterability was relatively insensitive to changes in operating conditions, provided the availability of hydrogen was adequate, for gas flow rates in the range 0.95 to 1.4 l S -1 , pulse frequencies of 0.5 and 0.75 Hz and mean residence times of the solids from 0.6 to 1.4 hours. Sinterability was shown to be improved either by use of higher input concentrations, or by use of a secondary flow of hydrogen (about 5 per cent of input) fed into the powder collection system and flowing countercurrent to the UO 2 product. The maximum throughput of 17 kg UO 2 h -1 (0.6 hours mean residence time) required only 120 per cent of the stoichiometric requirement at an input concentration of 50 vol.per cent with secondary hydrogen flow. Results are given for studies of the kinetics of reduction of calcined ammonia diuranate in hydrogen and the residence time distribution of solids in a pulsed fluidised bed. Estimates based on these data suggested that the overall conversion of ammonium diuranate to uranium dioxide in the continuously operated pulsed fluidised bed reactor was in excess of 99 per cent. Continuous stabilisation of the UO 2 product was demonstrated at 12 kg h -1 or UO 2 , in a 0.15 m diameter glass stabiliser, using 10 vol.per cent air in nitrogen and a temperature of about 50 0 C. (author)

  15. On the influence of thiamine and ammonium ions on alcoholic fermentation

    NARCIS (Netherlands)

    Maesen, Th.J.M.

    1953-01-01

    1. 1. In a glucose-sodium acetate medium of pH 5.6 the fermentation rate of bakers' yeast remains constant at a low level during several hours, while in the presence of ammonium sulphate it gradually increases. The rise is steeper in the presence of thiamine. 2. 2. After the ammonium ions have

  16. Field dissipation and storage stability of glufosinate ammonium and its metabolites in soil.

    Science.gov (United States)

    Zhang, Yun; Wang, Kai; Wu, Junxue; Zhang, Hongyan

    2014-01-01

    A simple analytical method was developed to measure concentrations of glufosinate ammonium and its metabolites, 3-methylphosphinico-propionic acid (MPP) and 2-methylphosphinico-acetic acid (MPA), in field soil samples. To determine the minimum quantification limit, samples were spiked at different levels (0.1, 0.5, and 1.0 mg/kg). Soil samples were extracted with ammonium hydroxide solution 5% (v/v), concentrated, and reacted with trimethyl orthoacetate (TMOA) in the presence of acetic acid for derivatization. The derivatives were quantified by gas chromatography (GC) using a flame photometric detector (FPD). The linear correlation coefficients of glufosinate ammonium, MPP, and MPA in soil were 0.991, 0.999, and 0.999, respectively. The recoveries of this method for glufosinate ammonium, MPP, and MPA in soil were 77.2-95.5%, 98.3-100.3%, and 99.3-99.6% with relative standard deviations (RSD) of 1.8-4.1%, 0.4-1.4%, and 1.3-2.0%, respectively. Glufosinate ammonium dissipated rapidly in soil to MPA in hours and gradually degraded to MPP. The half-life of glufosinate ammonium degradation in soil was 2.30-2.93 days in an open field. In soil samples stored at -20°C glufosinate ammonium was stable for two months. The results of this study should provide guidance for the safe application of the herbicide glufosinate ammonium to agricultural products and the environment.

  17. Effects of salinity induced by ammonium sulfate fertilizer on root and shoot growth of highbush blueberry

    Science.gov (United States)

    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...

  18. 77 FR 59377 - Solid Agricultural Grade Ammonium Nitrate from Ukraine: Final Results of the Expedited Second...

    Science.gov (United States)

    2012-09-27

    ... Ammonium Nitrate from Ukraine: Final Results of the Expedited Second Sunset Review of the Antidumping Duty... duty order on solid agricultural grade ammonium nitrate from Ukraine. The Department has conducted an... revocation of the antidumping duty order would be likely to lead to continuation or recurrence of dumping at...

  19. AMMONIUM TOXICITY AND NITRATE RESPONSE OF AXENICALLY GROWN DACTYLORHIZA-INCARNATA SEEDLINGS

    NARCIS (Netherlands)

    DIJK, E; ECK, N

    1995-01-01

    The response to ammonium- and nitrate-nitrogen of seedlings of the calcicole orchid species Dactylorhiza incarnata (L.) Soo was tested in axenic in vitro culture of c. 3-month-old protocorms. A pronounced toxicity of ammonium ions was observed. Seedlings raised from plants of a coastal population

  20. Factors affecting ammonium uptake in streams - an inter-biome perspective

    Science.gov (United States)

    Jackson R Webster; Partick J. Mulholland; Jennifer L. Tanks; H. Maurice Valett; Walter K. Dodds; Bruce J. Peterson; William B. Bowden; Clifford N. Dahm; Stuart Findlay; Stanley V. Gregory; Nancy B. Grimm; Stephen K. Hamilton; Sherri L. Johnson; Eugenia Marti; William H. McDowell; Judy L. Meyer; Donna D. Morrall; Steven A. Thomas; Wilfred M. Wollhem

    2003-01-01

    1. The Lotic Intersite Nitrogen experiment (LINX) was a coordinated study of the relationships between North American biomes and factors governing ammonium uptake in streams. Our objective was to relate inter-biome variability of ammonium uptake to physical, chemical and biological processes. 2. Data were collected from 11 streams ranging from arctic to tropical and...