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Sample records for ammonium thiocyanates

  1. Aqueous ammonium thiocyanate solutions as refractive index-matching fluids with low density and viscosity

    CERN Document Server

    Borrero-Echeverry, Daniel

    2016-01-01

    We show that aqueous solutions of ammonium thiocyanate (NH4SCN) can be used to match the index of refraction of several transparent materials commonly used in experiments, while maintaining low viscosity and density compared to other common refractive index-matching liquids. We present empirical models for estimating the index of refraction, density, and kinematic viscosity of these solutions as a function of temperature and concentration. Finally, we summarize some of the chemical compatibility of ammonium thiocyanate with materials commonly used in apparatus.

  2. Oxidation of ferrocene by thiocyanic acid in the presence of ammonium oxalate

    Energy Technology Data Exchange (ETDEWEB)

    Ruslin, Farah bt; Yamin, Bohari M. [School of Chemical Science and Food Technology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia (Malaysia)

    2014-09-03

    A flake-like crystalline salt was obtained from the reaction of ferrocene, oxalic acid and ammonium thiocyanate in ethanol The elemental analysis and spectroscopic data were in agreement with the preliminary X-ray molecular structure. The compound consists of four ferrocenium moieties and a counter anion consisting of two (tetraisothiocyanato)iron(III) linked by an oxalato bridging group in such a way that both iron central atoms adopt octahedral geometries.

  3. Characterization and electrical properties of polyvinyl alcohol based polymer electrolyte films doped with ammonium thiocyanate

    International Nuclear Information System (INIS)

    Highlights: • Polyvinyl alcohol (PVA). • Ammonium thiocyanate (NH4SCN). • Electrical conductivity. • Fractals. - Abstract: In this communication, films of polyvinyl alcohol (PVA) polymer complexed with ammonium thiocyanate (NH4SCN) salt were studied. XRD (X-ray diffraction) was used to study the complexation of salt with the polymer matrix and amorphicity in the films. DSC (differential scanning calorimetry) studies showed that the glass transition temperatures (Tg) of the PVA:NH4SCN complexed films were less than pristine PVA. Raman analysis was analyzed in order to study the change in the vibrational bands due to the complexation of salt with PVA. Optical micrographs confirm the fractal formation in 75:25 and 70:30 PVA:NH4SCN films. Ionic transference number was estimated by Wagner's polarization method and its large value indicates that conduction takes place mainly due to mobile ionic species. Maximum conductivity ∼10−3 S/cm at room temperature was obtained for 70:30 ratio of PVA: NH4SCN polymer electrolyte films

  4. Simultaneous removal of phenol, ammonium and thiocyanate from coke wastewater by aerobic biodegradation

    International Nuclear Information System (INIS)

    A laboratory-scale activated sludge plant composed of a 20 L volume aerobic reactor followed by a 12 L volume settling tank and operating at 35 deg. C was used to study the biodegradation of coke wastewater. The concentrations of ammonium nitrogen (NH4+-N), phenols, chemical oxygen demand (COD) and thiocyanate (SCN-) in the wastewater ranged between 504 and 2340, 110 and 350, 807 and 3275 and 185 and 370 mg/L, respectively. The study was undertaken with and without the addition of bicarbonate. The addition of this inorganic carbon source was necessary to favour nitrification, as the alkalinity of the wastewater was very low. Maximum removal efficiencies of 75%, 98% and 90% were obtained for COD, phenols and thyocianates, respectively, without the addition of bicarbonate. The concentration of ammonia increased in the effluent due to both the formation of NH4+ as a result of SCN- biodegradation and to organic nitrogen oxidation. A maximum nitrification efficiency of 71% was achieved when bicarbonate was added, the removals of COD and phenols being almost similar to those obtained in the absence of nitrification. Batch experiments were performed to study the influence of pH and alkalinity on the biodegradation of phenols and thiocyanate

  5. Technical Study on Gold Extraction by Ammonium Thiocyanate%硫氰酸铵法提金工艺研究

    Institute of Scientific and Technical Information of China (English)

    宋岷蔚; 刘菁; 俞海平

    2013-01-01

    With some sulfide-locked gold fine ore from Sichuan Province as raw material, comparative tests were conduced for gold extraction by cyanide process and by using ammonium thiocyanate respectively. The effects and characteristics of oxidants Fe3 + and MnO2 in gold leaching process with ammonium thiocyanate were explored. The gold leaching mechanism by cyanide process and by using ammonium thicyanate was also preliminarily investigated and analyzed. Results show that gold extraction by using ammonium thiocyanate, compared with gold cyanidation, can lead to a better result with gold leaching rate up to 96% while using Fe3 + as oxidant.%以四川某硫化物包裹型金矿石精金砂为原料,对比研究了氰化法和硫氰酸铵法的提金效果,考察了氧化剂Fe3+和MnO2在硫氰酸铵浸金工艺中的作用和特点,并对氰化法和硫氰酸铵法的浸出机理进行了初步探讨和分析.结果表明,硫氰酸铵法比氰化法有更好的提金效率;用Fe3+作氧化剂的硫氰酸铵浸金法提金效率可达96%.

  6. Bi(TFA3 and Bi(OTf3 Catalyzed Conversions of Epoxides to Thiiranes with Ammonium Thiocyanate and Thiourea under Non-Aqueous Conditions

    Directory of Open Access Journals (Sweden)

    Ahmad R. Khosropour

    2001-11-01

    Full Text Available Various epoxides are converted to their corresponding thiiranes in excellent yields with ammonium thiocyanate and thiourea under non-aqueous conditions in the presence of catalytic amounts of Bi(TFA3 and Bi(OTf3.

  7. Bi(TFA)3 and Bi(OTf)3 Catalyzed Conversions of Epoxides to Thiiranes with Ammonium Thiocyanate and Thiourea under Non-Aqueous Conditions

    OpenAIRE

    Khosropour, Ahmad R.; Iraj Mohammadpoor-Baltork

    2001-01-01

    Various epoxides are converted to their corresponding thiiranes in excellent yields with ammonium thiocyanate and thiourea under non-aqueous conditions in the presence of catalytic amounts of Bi(TFA)3 and Bi(OTf)3.

  8. Aqueous ammonium thiocyanate solutions as refractive index-matching fluids with low density and viscosity

    Science.gov (United States)

    Morrison, Benjamin C.; Borrero-Echeverry, Daniel

    2015-11-01

    Index-matching fluids play an important role in many fluid dynamics experiments, particularly those involving particle tracking, as they can be used to minimize errors due to distortion from the refraction of light across interfaces of the apparatus. Common index-matching fluids, such as sodium iodide solutions or mineral oils, often have densities or viscosities very different from those of water. This can make them undesirable for use as a working fluid when using commercially available tracer particles or at high Reynolds numbers. A solution of ammonium thiocyanate (NH4SCN) can be used for index-matching common materials such as borosilicate glass and acrylic, and has material properties similar to those of water (ν ~ 1 . 6 cSt and ρ ~ 1 . 1 g/cc). We present an empirical model for predicting the refractive index of aqueous NH4SCN solutions as a function of temperature and NH4SCN concentration that allows experimenters to develop refractive index matching solutions for various common materials. This work was supported by the National Science Foundation (CBET-0853691) and by the James Borders Physics Student Fellowship at Reed College.

  9. Oxygen-18 study of the mechanism of promoter action of thiocyanate ions in the electrosynthesis of persulfuric acid and ammonium persulfate at platinum anodes

    Energy Technology Data Exchange (ETDEWEB)

    Kasatkin, E.V.; Larchenko, L.I.; Potapova, G.F.

    1987-02-01

    The authors use labelled oxygen to study the involvement of water and sulfate ions in molecular oxygen evolution during the anodic synthesis of persulfuric acid and ammonium persulfate at a platinum anode in an electrolytic cell with and without thiocyanate as a promoter for the electrocatalytic reaction.

  10. Extraction of high-quality epidermal RNA after ammonium thiocyanate-induced dermo-epidermal separation of 4 mm human skin biopsies

    DEFF Research Database (Denmark)

    Clemmensen, Anders; Thomassen, Mads; Clemmensen, Ole;

    2009-01-01

    , and satisfactory amounts of high-quality RNA were obtained. Hybridization to Affymetrix HG_U133A 2.0 GeneChips showed that ammonium thiocyanate incubation had a minute effect on gene expression resulting in only one significantly downregulated gene (cystatin E/M). We conclude that epidermis can be reproducibly...

  11. Studies on extraction of beryllium from thiocyanate solutions by quaternary ammonium halides.

    Science.gov (United States)

    El-Yamani, I S; El-Messieh, E N

    A 0.4M tricaprylmethylammonium chloride solution in n-hexane was used for the quantitative extraction of beryllium from hydrochloric acid (pH 3) and 5M potassium thiocyanate. Beryllium was stripped from the organic phase with 1M sodium hydroxide, then determined volumetrically with bismuthyl perchlorate and bromocresol green indicator. Beryllium was extracted in presence of a large number of elements which are usually associated with it in beryl and in fission products of nuclear fuel.

  12. New approach to optimize operational conditions for the biological treatment of a high-strength thiocyanate and ammonium waste: pH as key factor.

    Science.gov (United States)

    Lay-Son, Meiling; Drakides, Christian

    2008-02-01

    Biological treatment of coke and steel-processing wastewaters has to satisfy both industrial economic needs and environmental protection regulations. Nevertheless, as some of the pollutants contained in these waters or produced during the treatment are highly toxic, an effective and safe treatment has proved to be difficult to obtain. This paper reports the study of a biological method for the treatment of wastewaters containing free cyanide, thiocyanate and ammonium (NH4). Laboratory-scale activated-sludge reactors were fed with a synthetic solution reproducing a steel-processing industrial wastewater and inoculated with the same industrial bacterial seeding used on-site (Ecosynergie Inc.). The results demonstrated that free cyanide and thiocyanate were efficiently degraded. Nevertheless, thiocyanate degradation and nitrification processes were actually inhibited by the free ammonia form (NH3) in place of the ionized NH4 form (NH4+) currently dosed and often unproperly named "ammonia" [IUPAC, 1997. In: McNaught, A.D., Wilkinson, A. (compilers). Compendium of Chemical Terminology. Royal Society of Chemistry, Cambridge, UK]. Optimum degradation rates were obtained for very narrow ranges of ammonia nitrogen (NH3-N) concentrations. This result can be explained by the role of pH, which mainly controls the NH3/NH4 equilibrium. Pollutants and NH3 concentrations influenced degradation rates of main pollutants. This influence was determined and expressed through elementary equations. Although the Michaelis-Menten equation could have been used to describe thiocyanate degradation, a Haldane-inhibition model was used to satisfactorily describe cyanide degradation. On the other hand, a slightly modified Haldane model was applied to describe both NH4 oxidation using NH3-N as substrate and thiocyanate degradation using NH3-N as inhibitor. These findings emphasize the role of pH on degradation rates and allow one to optimize operational conditions in the biological treatment of

  13. EQCM study of the electrodeposition of manganese in the presence of ammonium thiocyanate in chloride-based acidic solutions

    Energy Technology Data Exchange (ETDEWEB)

    Diaz-Arista, P. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica (CIDETEQ), Parque Tecnologico Sanfandila, Pedro Escobedo, Queretaro, A.P. 064, C.P. 76700, Queretaro (Mexico); Antano-Lopez, R. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica (CIDETEQ), Parque Tecnologico Sanfandila, Pedro Escobedo, Queretaro, A.P. 064, C.P. 76700, Queretaro (Mexico); Meas, Y. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica (CIDETEQ), Parque Tecnologico Sanfandila, Pedro Escobedo, Queretaro, A.P. 064, C.P. 76700, Queretaro (Mexico); Ortega, R. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica (CIDETEQ), Parque Tecnologico Sanfandila, Pedro Escobedo, Queretaro, A.P. 064, C.P. 76700, Queretaro (Mexico); Chainet, E. [LEPMI, ENSEEG, 1130, rue de la piscine, BP 45, 38402 Saint Martin d' Heres (France); Ozil, P. [LEPMI, ENSEEG, 1130, rue de la piscine, BP 45, 38402 Saint Martin d' Heres (France); Trejo, G. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica (CIDETEQ), Parque Tecnologico Sanfandila, Pedro Escobedo, Queretaro, A.P. 064, C.P. 76700, Queretaro (Mexico)]. E-mail: gtrejo@cideteq.mx

    2006-06-01

    The influence of ammonium thiocyanate (NH{sub 4}SCN) on the mechanism of manganese electrodeposition from a chloride-based acidic solution was investigated by cyclic voltammetry and electrochemical quartz crystal microbalance (EQCM). The EQCM data were represented as plots d{delta}m dt {sup -1} versus E, known as massograms. Because massograms are not affected by interference from the hydrogen evolution reaction, they clearly show the manganese reduction and oxidation processes. By comparing the voltammograms with their corresponding massograms, it was possible to differentiate mass changes due to faradaic processes from those due to non-faradaic processes. Morphology, chemical composition and structure of the manganese deposits formed in different potential ranges were analyzed by scanning electron microscopy (SEM), energy dispersion spectroscopy (EDS), and X-ray diffraction (XRD). The results showed that in the absence of NH{sub 4}SCN, Mn(OH){sub 2(s)} is formed in the potential range -1.1 to -0.9 V due to the hydrogen evolution reaction in this region. At more cathodic potentials, the deposition of {beta}-manganese and the inclusion of Mn(OH){sub 2(s)} into the deposit occur; both of these species underwent dissolution by non-faradaic processes during the anodic scan. In the presence of NH{sub 4}SCN, the formation of {alpha}- and {gamma}-manganese was observed. When the potential was {<=}-1.8 V and [NH{sub 4}SCN] exceeded 0.3 M, the {alpha}-manganese phase was favored.

  14. 2-Aminocyclohexan-1-aminium thiocyanate

    OpenAIRE

    Halima F. Salem; Siti Aishah Hasbullah; Yamin, Bohari M.

    2012-01-01

    The title compound, C6H15N2+·NCS−, was obtained unexpectedly from the reaction mixture of benzoyl chloride, ammonium thiocyanate and cyclohexane-1,2-diamine. The cyclohexane ring adopts a chair conformation. In the crystal, N—H...S and N—H...N interactions involving the thiocyanate anion and both the amine and the aminium N atoms link the molecules, forming two-dimensional networks parallel to (001).

  15. 2-Aminocyclohexan-1-aminium thiocyanate

    Directory of Open Access Journals (Sweden)

    Halima F. Salem

    2012-06-01

    Full Text Available The title compound, C6H15N2+·NCS−, was obtained unexpectedly from the reaction mixture of benzoyl chloride, ammonium thiocyanate and cyclohexane-1,2-diamine. The cyclohexane ring adopts a chair conformation. In the crystal, N—H...S and N—H...N interactions involving the thiocyanate anion and both the amine and the aminium N atoms link the molecules, forming two-dimensional networks parallel to (001.

  16. SelectfluorTM: A novel and efficient reagent for the rapid -thiocyanation of ketones

    Indian Academy of Sciences (India)

    Dezhen Wu; Xiaojuan Yang; Liqiang Wu

    2012-07-01

    The direct α-thiocyanation of ketones with ammonium thiocyanate has been achieved using SelectfluorTM under mild and neutral conditions to produce -ketothiocyanates, in excellent yields and with high selectivity.

  17. Rapid Determination of Iron in Water by Modified Thiocyanate Method

    OpenAIRE

    D. C. Goswami; H. Kalita

    1988-01-01

    A rapid spectrophotometric method for determination of iron in water by oxidising ferrous iron with ceric ammonium sulphate at roomtemperature followed by formation of ferric thiocyanate colour complexwith potassium thiocyanate has been described. The method is simple and rapid as compared to other standard methods used in water analysis and iron content of water upto 5 ppm can be determined by this method with a maximum error of 2.8 per cent

  18. Rapid Determination of Iron in Water by Modified Thiocyanate Method

    Directory of Open Access Journals (Sweden)

    D. C. Goswami

    1988-04-01

    Full Text Available A rapid spectrophotometric method for determination of iron in water by oxidising ferrous iron with ceric ammonium sulphate at roomtemperature followed by formation of ferric thiocyanate colour complexwith potassium thiocyanate has been described. The method is simple and rapid as compared to other standard methods used in water analysis and iron content of water upto 5 ppm can be determined by this method with a maximum error of 2.8 per cent

  19. Wet oxidation of real coke wastewater containing high thiocyanate concentration.

    Science.gov (United States)

    Oulego, Paula; Collado, Sergio; Garrido, Laura; Laca, Adriana; Rendueles, Manuel; Díaz, Mario

    2014-01-01

    Coke wastewaters, in particular those with high thiocyanate concentrations, represent an important environmental problem because of their very low biodegradability. In this work, the treatment by wet oxidation of real coke wastewaters containing concentrations of thiocyanate above 17 mM has been studied in a 1-L semi-batch reactor at temperatures between 453 and 493 K, with total oxygen pressures in the range of 2.0-8.0 MPa. A positive effect of the matrix of real coke wastewater was observed, resulting in faster thiocyanate degradation than was obtained with synthetic wastewaters. Besides, the effect of oxygen concentration and temperature on thiocyanate wet oxidation was more noticeable in real effluents than in synthetic wastewaters containing only thiocyanate. It was also observed that the degree of mineralization of the matrix organic compounds was higher when the initial thiocyanate concentration increased. Taking into account the experimental data, kinetic models were obtained, and a mechanism implying free radicals was proposed for thiocyanate oxidation in the matrix considered. In all cases, sulphate, carbonates and ammonium were identified as the main reaction products of thiocyanate wet oxidation. PMID:24269931

  20. Exploration Test on Gold Extraction from Arsenopyrite Gold Concentrate with Oxidation Pressure Leaching Process in Ammonium Thiocyanate-Ammonia System%某毒砂金矿硫氰酸盐氨性体系加压氧化提金探索试验

    Institute of Scientific and Technical Information of China (English)

    胡燕清; 杨声海; 陈永明

    2012-01-01

    对某毒砂金矿进行了硫氰酸盐氨性体系氧压提取金的探索试验,考察了反应温度、Cu2+浓度、浸出时间、液固比、氨水浓度、氧分压和硫氰酸铵浓度等对金浸出率的影响.结果表明,在下述优化条件下金浸出率为61.7%,即硫氰酸铵浓度3 mol/L,液固比5:1,反应温度150℃,浸出时间6h,搅拌速度750r/min,氨水浓度4.64 mo/L,铜加入量1.5 g/L.而经400℃焙烧预处理后金浸出率达到86.2%.%The exploration test on gold extraction from arsenopyrite gold concentrate with oxidation pressure leaching process in ammonium thiocyanate-ammonia system was performed. The effects of leaching temperature,copper concentration, leaching time, ratio of liquid to solid (L/S), ammonia concentration, oxygen pressure, and the concentration of ammonium thiocyanate on gold leaching rate were studied. The results show that the gold leaching ratio is 61. 7% under the optimum conditions including NH4SCN concentration of 3 mol/L, L/S=5, leaching temperature of 150 °C , leaching time of 6 hours, stirring speed of 750 r/min, ammonia concentration of 4. 64 mol/L, and copper dosage of 1. 5 g/L. The gold leaching ratio can leach 86. 2% after the pretreatment of roasting at 400℃.

  1. 2-Methylbenzimidazolium thiocyanate

    OpenAIRE

    Shayma A. Shaker; Hamid Khaledi; Hapipah Mohd Ali

    2010-01-01

    In the crystal structure of the title compound, C8H9N2+·SCN−, the nearly planar 2-methylbenzimidazolium cation [r.m.s. deviation = 0.0123 (4) Å] is perpendicular to a mirror plane and the methyl H atoms are disordered about the mirror plane with equal occupancies. The thiocyanate anion also lies on a mirror plane. N—H...N hydrogen bonds link the components into an infinite chain along the b axis.

  2. Titrimetric determination of thiocyanate in solutions of the hafnium-zirconium separation process

    International Nuclear Information System (INIS)

    The control of the thiocyanate concentration is necessary during the process of separating hafnium from zirconium by the hexone-thiocyanate method. Said control is carried out by titrimetric determination of thiocyanate in aqueous and organic solutions containing hydrochloric acid and ammonium thiocyanate in presence or absence of zirconium and/or hafnium. The method consists in a redox volumetric analysis using a cerium (IV) salt as titrating agent, and ferroine as the final point indicator. Owing to the instability of thiocyanate in an acid medium it is necessary to know previously if the decomposition of solutions with different concentration of ammonium thiocyanate and hydrochloric acid may have an influence upon the analytic results or may even invalidate them. In order to obtain reliable results, it must be taken into account that the stability of the solutions depends on the thiocyanate concentration, the acidity and the time elapsed from the moment the sample is taken until the test is performed. The decomposition process can be slowed down by cooling the solutions. This method allows to control the plant and does not require any special equipment. (M.E.L)

  3. Glycerin derivatives with thiocyanic group

    International Nuclear Information System (INIS)

    Present article is devoted to glycerin derivatives with thiocyanic group. The results of studies of the nucleophilic substitution reaction of chlorine atom in linear and cyclic glycerin derivatives on thiocyanic group were considered. The composition, structure and purity of synthesized substances was defined by means of element analysis, molecular refraction, infrared spectroscopy, and thin-layer chromatography methods.

  4. 2-Methylbenzimidazolium thiocyanate

    Directory of Open Access Journals (Sweden)

    Shayma A. Shaker

    2010-11-01

    Full Text Available In the crystal structure of the title compound, C8H9N2+·SCN−, the nearly planar 2-methylbenzimidazolium cation [r.m.s. deviation = 0.0123 (4 Å] is perpendicular to a mirror plane and the methyl H atoms are disordered about the mirror plane with equal occupancies. The thiocyanate anion also lies on a mirror plane. N—H...N hydrogen bonds link the components into an infinite chain along the b axis.

  5. 氯化钠-正丙醇-硫氰酸铵-水体系析相萃取分离和富集锡(Ⅳ)%Separation and enrichment of stannum (Ⅳ) by phase extraction in sodium chloride-1-propanol-ammonium thiocyanate-water system

    Institute of Scientific and Technical Information of China (English)

    李玉玲; 陈彬; 马万山

    2013-01-01

    The behavior and conditions for extraction separation and enrichment of stannum (Ⅳ) from other metal ions in sodium chloride-1-propanol-ammonium thiocyanate-water system were investigated.The results showed that 1-propanol aqueous solution could be well divided into two phases in presence of sodium chloride.During the phase separation process,[Sn(SCN)5~6] [(5~6)-4]-formed from stannum (Ⅳ) and ammonium thiocyanate could reacted with protonized 1-propanol of C3H7OH2 + to form associated complex of [Sn(SCN)5~6][C3 H7OH2]1-2,which could be fully extracted by 1-propanol phase.When acidity of the solution was fixed at pH 2.0,and the concentration of 1-propanol,ammonium thiocyanate and sodium chloride was 30%(V/V),0.09 mol/L and 0.17 g/mL,respectively,the extraction yield of stannum(Ⅳ) was more than 98.3%.Simultaneously,Fe(Ⅱ),Ni(Ⅱ),Pb(Ⅱ),Al (Ⅲ),Mg(Ⅱ),Mn(Ⅱ),Ce(Ⅲ),Cr(Ⅲ),Zn(Ⅱ),Ag(Ⅰ),Cd(Ⅱ)and V(V) could not be extracted,realizing the separation of stannum (Ⅳ) from these metal ions.The method has been applied to the separation and determination of stannum (Ⅳ) in Pb-Ca-Sn-Al alloy sample with recovery of 97.4% and relative standard deviation(n=7) of 2.1%.%研究了氯化钠-正丙醇-硫氰酸铵-水体系析相萃取分离和富集Sn(Ⅳ)的行为及与一些金属离子分离的条件.结果表明,氯化钠能使正丙醇的水溶液分成两相,在分相过程中,Sn(Ⅳ)和硫氰酸铵生成的[Sn(SCN)5~6][(5~6)-4]-与质子化正丙醇C3H7OH2+形成的缔合物[Sn (SCN)5~6][C3H7OH2]1-2能被正丙醇相完全萃取.固定溶液酸度为pH 2,当正丙醇、硫氰酸铵和氯化钠的浓度分别为30% (V/V)、0.09 mol/L和0.17 g/mL时,Sn(Ⅳ)的萃取率在98.3%以上,Fe(Ⅱ)、Ni(Ⅱ)、Pb(Ⅱ)、Al(Ⅲ)、Mg(Ⅱ)、Mn(Ⅱ)、Ce(Ⅲ)、Cr(Ⅲ)、Zn(Ⅱ)、Ag(Ⅰ)、Cd(Ⅱ)和V(Ⅴ)不被萃取,实现了Sn(Ⅳ)与上述金属离子的分离.方法用于Pb-Ca-Sn-Al合金中Sn的分离和测定,平均回收率为97.4

  6. Floatation separation of cobalt with ammonium thiocyanate-crystal violet -aqua system%硫氰酸铵-结晶紫-H2O 体系浮选分离钴

    Institute of Scientific and Technical Information of China (English)

    李全民; 赵春霞; 卫伟

    2001-01-01

    研究了硫氰酸铵-结晶紫-H2O 体系浮选分离 Co(Ⅱ)与 Ni(Ⅱ)、Fe(Ⅲ)、Mn(Ⅱ)、Al(Ⅲ)、Cd(Ⅱ) 等常见离子的方法及条件。当 NaCl 用量为 1 g,硫氰酸铵(0.1 mol/L)和结晶紫(1×10-3 mol/L)溶液用量分别为 1.5 mL 和 2.5 mL,总体积为 10 mL 时,控制 pH 1.0~2.0,即可实现 Co(Ⅱ) 与上述离子的分离。%The flotation separation behaviour of cobalt with NH4SCN-CV(crystal violet)-H2O system and the conditions for separation of cobalt from other metal ions were studied. In the aqueous solution, Co(Ⅱ) was precipitated by reaction with thiocyanate and crystal violet, and the precipitate could be separated from aqueous solution by filtering. Under the optional conditions, the completely separation of Co(Ⅱ) from Zn(Ⅱ), Fe(Ⅲ), Cd(Ⅱ), Ni(Ⅱ), Mn(Ⅱ), Al(Ⅲ) was realized by floatation at pH 1.0~2.0.

  7. Flow-through Bulk Optode for Spectrophotometric Determination of Thiocyanate and Its Application to Water and Saliva Analysis

    Directory of Open Access Journals (Sweden)

    José Fernández

    2006-10-01

    Full Text Available A flow-through spectrophotometric bulk optode for the flow-injectiondetermination of thiocyanate is described. As active constituents, the optode incorporatesthe lipophilized pH indicator 5-octadecanoyloxy-2-(4-nitrophenylazophenol andmethyltridodecyl ammonium chloride, dissolved in a plasticized poly(vinylchloridemembrane entrapped in a cellulose support. The optode is applied, in conjunction with theflow injection technique, to the determination of thiocyanate at pH 7.5 (TRIS/H2SO4. Thesensor is readily regenerated with a 10-2 M NaOH carrier solution. The analyticalcharacteristics of this optode with respect to thiocyanate response time, dynamicmeasurement range, reproducibility and selectivity are discussed. The proposed FI methodis applied to the determination of thiocyanate in waters from different sources and in humansaliva samples in order to distinguish between smokers and non-smokers.

  8. Microbial thiocyanate utilization under highly alkaline conditions.

    Science.gov (United States)

    Sorokin, D Y; Tourova, T P; Lysenko, A M; Kuenen, J G

    2001-02-01

    Three kinds of alkaliphilic bacteria able to utilize thiocyanate (CNS-) at pH 10 were found in highly alkaline soda lake sediments and soda soils. The first group included obligate heterotrophs that utilized thiocyanate as a nitrogen source while growing at pH 10 with acetate as carbon and energy sources. Most of the heterotrophic strains were able to oxidize sulfide and thiosulfate to tetrathionate. The second group included obligately autotrophic sulfur-oxidizing alkaliphiles which utilized thiocyanate nitrogen during growth with thiosulfate as the energy source. Genetic analysis demonstrated that both the heterotrophic and autotrophic alkaliphiles that utilized thiocyanate as a nitrogen source were related to the previously described sulfur-oxidizing alkaliphiles belonging to the gamma subdivision of the division Proteobacteria (the Halomonas group for the heterotrophs and the genus Thioalkalivibrio for autotrophs). The third group included obligately autotrophic sulfur-oxidizing alkaliphilic bacteria able to utilize thiocyanate as a sole source of energy. These bacteria could be enriched on mineral medium with thiocyanate at pH 10. Growth with thiocyanate was usually much slower than growth with thiosulfate, although the biomass yield on thiocyanate was higher. Of the four strains isolated, the three vibrio-shaped strains were genetically closely related to the previously described sulfur-oxidizing alkaliphiles belonging to the genus Thioalkalivibrio. The rod-shaped isolate differed from the other isolates by its ability to accumulate large amounts of elemental sulfur inside its cells and by its ability to oxidize carbon disulfide. Despite its low DNA homology with and substantial phenotypic differences from the vibrio-shaped strains, this isolate also belonged to the genus Thioalkalivibrio according to a phylogenetic analysis. The heterotrophic and autotrophic alkaliphiles that grew with thiocyanate as an N source possessed a relatively high level of cyanase

  9. Extraction of zinc and cadmium thiocyanate complexes in the presence of pyridine and some metal ion separations

    International Nuclear Information System (INIS)

    Extraction of zinc(II) and cadmium(II) from ammonium thiocyanate solutions has been studied in benzene in the presence of pyridine. The effect of such variables as the pH of aqueous phase and concentration of metal, thiocyanate and pyridine on extraction has been investigated and the extracting species identified. The extraction behaviour of silver(I), manganese(II), cobalt(II), mercury(II) and thallium(III) has also been studied under identical conditions and some binary metal ion separations of analytical and radiochemical importance are reported. (author)

  10. Crystal structure of cyclohexylammonium thiocyanate

    OpenAIRE

    Abdulaziz A. Bagabas; Sultan B. Alhoshan; Hazem A. Ghabbour; C S Chidan Kumar; Hoong-Kun Fun

    2015-01-01

    In the title salt, C6H11NH3+·SCN−, the cyclohexylammonium ring adopts a slightly distorted chair conformation. The ammonium group occupies an equatorial position to minimize 1,3 and 1,5 diaxial interactions. In the crystal, the components are linked by N—H...N and N—H...S hydrogen-bonding interactions, resulting in a three-dimensional network.

  11. Crystal structure of cyclohexylammonium thiocyanate

    Directory of Open Access Journals (Sweden)

    Abdulaziz A. Bagabas

    2015-01-01

    Full Text Available In the title salt, C6H11NH3+·SCN−, the cyclohexylammonium ring adopts a slightly distorted chair conformation. The ammonium group occupies an equatorial position to minimize 1,3 and 1,5 diaxial interactions. In the crystal, the components are linked by N—H...N and N—H...S hydrogen-bonding interactions, resulting in a three-dimensional network.

  12. Dynamical Complexity in Electrochemical Oxidations of Thiocyanate

    Institute of Scientific and Technical Information of China (English)

    LIU,LI; FENG,Jiamin; WU,Guoguang; L(U),Xiaoli; Gao,Qingyu

    2009-01-01

    Kinetics and mechanism of the electrochemical oxidation of thiocyanate on a Pt electrode were investigated by using various electrochemical methods,in which both current and potential oscillations have been observed.Cyclic voltarnmetry measurements illustrate that the oxidation process consists of two steps.In addition to the oscillatory behavior,the system also exhibits bistability,in which the oxidation could be switched between a high and a low current density states with a temporal potential perturbation.The presence of inert ions with stronger absorption also induces transitions from oscillatory to steady reactions in the thiocyanate system.

  13. Synthesis and characterization of bis nitrato[4-hydroxyacetophenonesemicarbazone) nickel(II) complex as ionophore for thiocyanate-selective electrode.

    Science.gov (United States)

    Chandra, Sulekh; Hooda, Sunita; Tomar, Praveen Kumar; Malik, Amrita; Kumar, Ankit; Malik, Sakshi; Gautam, Seema

    2016-05-01

    The PVC based-ion selective electrode viz., bis nitrato[4-hydroxyacetophenone semicarbazone] nickel(II) as an ionophore was prepared for the determination of thiocyanate ion. The ionophore was characterized by FT-IR, UV-vis, XRD, magnetic moment and elemental analysis (CHN). On the basis of spectral studies an octahedral geometry has been assigned. The best performance was obtained with a membrane composition of 31% PVC, 63% 2-nitrophenyl octylether, 4.0% ionophore and 2.0% trioctylmethyl ammonium chloride. The electrode exhibited an excellent Nernstian response to SCN(-) ion ranging from 1.0 × 10(-7) to 1.0 × 10(-1)M with a detection limit of 8.6 × 10(-8)M and a slope of -59.4 ± 0.2 mV/decade over a wide pH range (1.8-10.7) with a fast response time (6s) at 25 °C. The proposed electrode showed high selectivity for thiocyanate ion over a number of common inorganic and organic anions. It was successfully applied to direct determination of thiocyanate in biological (urine and saliva) samples in order to distinguish between smokers and non-smokers, environmental samples and as an indicator electrode for titration of thiocyanate ions with AgNO3 solution. PMID:26952393

  14. A novel pink-pigmented facultative methylotroph, Methylobacterium thiocyanatum sp. nov., capable of growth on thiocyanate or cyanate as sole nitrogen sources.

    Science.gov (United States)

    Wood, A P; Kelly, D P; McDonald, I R; Jordan, S L; Morgan, T D; Khan, S; Murrell, J C; Borodina, E

    1998-02-01

    The isolation and properties of a novel species of pink-pigmented methylotroph, Methylobacterium thiocyanatum, are described. This organism satisfied all the morphological, biochemical, and growth-substrate criteria to be placed in the genus Methylobacterium. Sequencing of the gene encoding its 16S rRNA confirmed its position in this genus, with its closest phylogenetic relatives being M. rhodesianum, M. zatmanii and M. extorquens, from which it differed in its ability to grow on several diagnostic substrates. Methanol-grown organisms contained high activities of hydroxypyruvate reductase -3 micromol NADH oxidized min-1 (mg crude extract protein)-1], showing that the serine pathway was used for methylotrophic growth. M. thiocyanatum was able to use thiocyanate or cyanate as the sole source of nitrogen for growth, and thiocyanate as the sole source of sulfur in the absence of other sulfur compounds. It tolerated high concentrations (at least 50 mM) of thiocyanate or cyanate when these were supplied as nitrogen sources. Growing cultures degraded thiocyanate to produce thiosulfate as a major sulfur end product, apparently with the intermediate formation of volatile sulfur compounds (probably hydrogen sulfide and carbonyl sulfide). Enzymatic hydrolysis of thiocyanate by cell-free extracts was not demonstrated. Cyanate was metabolized by means of a cyanase enzyme that was expressed at approximately sevenfold greater activity during growth on thiocyanate [Vmax 634 +/- 24 nmol NH3 formed min-1 (mg protein)-1] than on cyanate [89 +/- 9 nmol NH3 min-1 (mg protein)-1]. Kinetic study of the cyanase in cell-free extracts showed the enzyme (1) to exhibit high affinity for cyanate (Km 0.07 mM), (2) to require bicarbonate for activity, (3) to be subject to substrate inhibition by cyanate and competitive inhibition by thiocyanate (Ki 0.65 mM), (4) to be unaffected by 1 mM ammonium chloride, (5) to be strongly inhibited by selenocyanate, and (6) to be slightly inhibited by 5 m

  15. Thiocyanate hydrolase, the primary enzyme initiating thiocyanate degradation in the novel obligately chemolithoautotrophic halophilic sulfur-oxidizing bacterium Thiohalophilus thiocyanoxidans.

    Science.gov (United States)

    Bezsudnova, Ekaterina Yu; Sorokin, Dimitry Yu; Tikhonova, Tamara V; Popov, Vladimir O

    2007-12-01

    Thiohalophilus thiocyanoxidans is a first halophilic sulfur-oxidizing chemolithoautotrophic bacterium capable of growth with thiocyanate as an electron donor at salinity up to 4 M NaCl. The cells, grown with thiocyanate, but not with thiosulfate, contained an enzyme complex hydrolyzing thiocyanate to sulfide and ammonia under anaerobic conditions with carbonyl sulfide as an intermediate. Despite the fact of utilization of the , high cyanase activity was also detected in thiocyanate-induced cells. Three-stage column chromotography resulted in a highly purified thiocyanate-hydrolyzing protein with an apparent molecular mass of 140 kDa that consists of three subunits with masses 17, 19 and 29 kDa. The enzyme is a Co,Fe-containing protein resembling on its function and subunit composition the enzyme thiocyanate hydrolase from the Betaproteobacterium Thiobacillus thioparus. Cyanase, copurified with thiocyanate hydrolase, is a bisubstrate multisubunit enzyme with an apparent subunit molecular mass of 14 kDa. A possible role of cyanase in thiocyanate degradation by T. thiocyanoxidans is discussed.

  16. Copper thiocyanate: polytypes, defects, impurities, and surfaces

    Science.gov (United States)

    Tsetseris, Leonidas

    2016-07-01

    Copper thiocyanate (CuSCN) is an established solid state dye in solar cells and has emerged as a key material for applications in transparent conductors and solution-processed thin film transistors. Here we report the results of density-functional theory calculations on several fundamental properties related to the performance of CuSCN in the above-mentioned systems. We describe the structural and electronic properties of CuSCN phases and show that the material is prone to polytypism. We also perform a systematic study on various defects and hydrogen impurities and determine their effect on the electronic properties of the host system, particularly with respect to doping. Finally, we show that non-polar surfaces have low formation energies, suggesting easy cleavage along certain directions.

  17. Adsorption removal of thiocyanate from aqueous solution by calcined hydrotalcite

    Institute of Scientific and Technical Information of China (English)

    LI Yu-jiang; YANG Min; ZHANG Xiao-jin; WU Tao; CAO Nan; WEI Na; BI Yan-jun; WANG Jing

    2006-01-01

    A hydrotalcite with Mg/Al molar ratio 2 was prepared by co-precipitation method and was characterized by XRD,TG/DTA, Zeta potential and BET surface area. The hydrotalcite was calcined at 500℃, with the dehydration from interlayer, the dehydroxilation from the brucite-like layer and the decomposition of carbonate successively, transformed into the mixed oxide type.The removal of thiocyanate from aqueous solution by using the original hydrotalcite and calcined hydrotalcite (HTC-500) was investigated. The results showed that the thiocyanate adsorption capacity of calcined hydrotalcite was much higher than that of the original form. Calcined hydrotalcite was particularly effective at removing thiocyanate, and that the effective range of pH for the thiocyanate removal are between 5.5-10.0. The experimental data of thiocyanate removal fit nicely with Langmuir isotherm, and the saturated adsorption uptake was 96.2 mg SCN-/g HTC-500. The adsorption ofthiocyanate by calcined hydrotalcite follows first-order kinetics. And the intercalation to the structure recovery for calcined hydrotalcite. But the presence of additional anions could affect the adsorption behavior of thiocyanate.

  18. Electrochemical study in molten potassium thiocyanate; Etude electrochimique dans le thiocyanate de potassium fondu

    Energy Technology Data Exchange (ETDEWEB)

    Metzger, G. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1964-07-01

    We have studied in this work the electrochemical properties of molten potassium thiocyanate. The melting point of this salt is 173 deg C and we have chosen to work at 195 deg C. The molten salted is dissociated into K{sup +} and SCN{sup -} ions; since the K{sup +} ions are very difficult to reduce it is the oxido-reduction reaction of the SCN{sup -} ion which limits the electro-active zone of the solvent. We have shown that SCN{sup -} behaves as an addition compound of S{sup 0} and CN{sup -}.analysis of the products formed during the oxidation and the coulometric reduction of the bath shows that the electrochemical reactions which limit the electro-active zone of the solvent are the following: SCN{sup -} + 2 e {yields} S{sup 2-} + CN{sup -} SCN{sup -} + 2 e {yields} S{down_arrow} + 1/2 (CN){sup -}{sub 2} We have shown that it is possible also to carry out the chemical oxidation of the thiocyanate by introducing an oxidising cation such as Fe{sup 3+} or Cu{sup 2+}. This reaction leads to the same chemical species as the electrochemical oxidation. With respect to the Ag{down_arrow} / Ag 0.1 M electrode taken as reference, the electro-active limits are the following: from - 1.050 V to + 0.750 V for a platinum electrode from - 1.350 V to + 0.050 V for a mercury drop electrode. We have studied the electrochemical behaviour of a certain number of ions in the molten salt; by plotting the intensity-potential curves it has been possible to determine the half-wave potentials of several cations: Pb{sup 2+}, Sn{sup 2+}, Fe{sup 2+}, Cd{sup 2+}, Zn{sup 2+}, Hg{sup 2+}{sub 2}, Hg{sup 2+}, Cu{sup +}, Co{sup 2+}, Ni{sup 2+}, Cr{sup 3+}. A comparison of the potential values found in the thiocyanate with those which are already known for other molten solvents has made it possible for us to find parallels between the properties of the thiocyanate and those of certain salts such as molten chlorides or nitrates. Thus the complexing properties of SCN{sup -} with respect to Cu

  19. The thiocyanate anion as a polydentate halogen bond acceptor

    OpenAIRE

    Cauliez, Pascal; Polo, Victor; Roisnel, Thierry; Llhusar, Rosa; Fourmigué, Marc

    2010-01-01

    International audience Co-crystallisation of the Et4N+ or n-Bu4N+ salts of the thiocyanate anion with o-, m- and p-diodoperfluorobenzene or the sym-trifluorotriiodobenzene allowed for the isolation of six different salts which were structurally characterized by single crystal X-ray diffraction. Halogen bonding interactions are observed between the neutral iodinated molecules acting as halogen bond donors and the S or N ends of the thiocyanate anion, with a variety of bonding modes (termina...

  20. [Mechanism of cyanide and thiocyanate decomposition by an association of Pseudomonas putida and Pseudomonas stutzeri strains].

    Science.gov (United States)

    Grigor'eva, N V; Kondrat'eva, T F; Krasil'nikova, E N; Karavaĭko, G I

    2006-01-01

    The intermediate and terminal products of cyanide and thiocyanate decomposition by individual strains of the genus Pseudomonas, P. putida strain 21 and P. stutzeri strain 18, and by their association were analyzed. The activity of the enzymes of nitrogen and sulfur metabolism in these strains was compared with that of the collection strains P. putida VKM B-2187T and P. stutzeri VKM B-975T. Upon the introduction of CN- and SCN- into cell suspensions of strains 18 and 21 in phosphate buffer (pH 8.8), the production of NH4+ was observed. Due to the high rate of their utilization, NH3, NH4+, and CNO- were absent from the culture liquids of P. putida strain 21 and P. stutzeri strain 18 grown with CN- or SCN-. Both Pseudomonas strains decomposed SCN- via cyanate production. The cyanase activity was 0.75 micromol/(min mg protein) for P. putida strain 21 and 1.26 micromol/(min mg protein) for P. stutzeri strain 18. The cyanase activity was present in the cells grown with SCN- but absent in cells grown with NH4+. Strain 21 of P. putida was a more active CN- decomposer than strain 18 of P. stutzeri. Ammonium and CO2 were the terminal nitrogen and carbon products of CN- and SCN- decomposition. The terminal sulfur products of SCN- decomposition by P. stutzeri strain 18 and P. putida strain 21 were thiosulfate and tetrathionate, respectively. The strains utilized the toxic compounds in the anabolism only, as sources of nitrogen (CN- and SCN-) and sulfur (SCN-). The pathway of thiocyanate decomposition by the association of bacteria of the genus Pseudomonas is proposed based on the results obtained.

  1. Development of a PBPK model of thiocyanate in rats with an extrapolation to humans: A computational study to quantify the mechanism of action of thiocyanate kinetics in thyroid.

    Science.gov (United States)

    Willemin, Marie-Emilie; Lumen, Annie

    2016-09-15

    Thyroid homeostasis can be disturbed due to thiocyanate exposure from the diet or tobacco smoke. Thiocyanate inhibits both thyroidal uptake of iodide, via the sodium-iodide symporter (NIS), and thyroid hormone (TH) synthesis in the thyroid, via thyroid peroxidase (TPO), but the mode of action of thiocyanate is poorly quantified in the literature. The characterization of the link between intra-thyroidal thiocyanate concentrations and dose of exposure is crucial for assessing the risk of thyroid perturbations due to thiocyanate exposure. We developed a PBPK model for thiocyanate that describes its kinetics in the whole-body up to daily doses of 0.15mmol/kg, with a mechanistic description of the thyroidal kinetics including NIS, passive diffusion, and TPO. The model was calibrated in a Bayesian framework using published studies in rats. Goodness-of-fit was satisfactory, especially for intra-thyroidal thiocyanate concentrations. Thiocyanate kinetic processes were quantified in vivo, including the metabolic clearance by TPO. The passive diffusion rate was found to be greater than NIS-mediated uptake rate. The model captured the dose-dependent kinetics of thiocyanate after acute and chronic exposures. Model behavior was evaluated using a Morris screening test. The distribution of thiocyanate into the thyroid was found to be determined primarily by the partition coefficient, followed by NIS and passive diffusion; the impact of the latter two mechanisms appears to increase at very low doses. Extrapolation to humans resulted in good predictions of thiocyanate kinetics during chronic exposure. The developed PBPK model can be used in risk assessment to quantify dose-response effects of thiocyanate on TH. PMID:27445130

  2. Removal of phenols, thiocyanate and ammonium from coal gasification wastewater using moving bed biofilm reactor.

    Science.gov (United States)

    Li, Hui-qiang; Han, Hong-jun; Du, Mao-an; Wang, Wei

    2011-04-01

    A laboratory-scale moving bed biofilm reactor (MBBR) with a volume of 4 L was used to study the biodegradation of coal gasification wastewater. Maximum removal efficiencies of 81%, 89%, 94% and 93% were obtained for COD, phenols, SCN(-) and NH(4)(+)-N, respectively. NO(2)(-)-N accumulation induced increase of effluent COD concentration when the hydraulic residence time (HRT) decreased. Phenols removal was not affected when the HRT decreased from 48 to 32 h. Effluent SCN(-) and NH(4)(+)-N concentration increased with the decrease of the HRT, and decreased gradually when the HRT returned to 48 h. Batch experiments were carried out to study performance of the suspended and attached growth biomass in the MBBR.

  3. Removal of phenols, thiocyanate and ammonium from coal gasification wastewater using moving bed biofilm reactor

    Energy Technology Data Exchange (ETDEWEB)

    Li, H.Q.; Han, H.J.; Du, M.A.; Wang, W. [Harbin Institute of Technology, Harbin (China)

    2011-04-15

    A laboratory-scale moving bed biofilm reactor (MBBR) with a volume of 4 L was used to study the biodegradation of coal gasification wastewater. Maximum removal efficiencies of 81%, 89%, 94% and 93% were obtained for COD, phenols, SCN{sup -} and NH{sub 4}{sup +}-N, respectively. NO{sub 2}{sup -}-N accumulation induced increase of effluent COD concentration when the hydraulic residence time (HRT) decreased. Phenols removal was not affected when the HRT decreased from 48 to 32 h. Effluent SCN{sup -} and NH{sub 4}{sup +}-N concentration increased with the decrease of the HRT, and decreased gradually when the HRT returned to 48 h. Batch experiments were carried out to study performance of the suspended and attached growth biomass in the MBBR.

  4. Transition metal complexes with pyrazole-based ligands.Part 29. Reactions of zinc(II) and mercury(II) thiocyanate with 4-acetyl-3-amino-5-methylpyrazole

    OpenAIRE

    KATALIN MÉSZÁROS SZÉCSÉNYI; BERTA HOLLÓ; VUKADIN M. LEOVAC; Bogdanović, Goran A.; Jaćimović, Željko K.

    2009-01-01

    The work is concerned with the crystal and molecular structures of zinc(II) and mercury(II) complexes with 4-acetyl-3-amino-5-methyl-pyrazole (aamp) of the coordination formulae [Zn(NCS)2(aamp)2] and (Haamp)2[Hg(SCN)4]. The zinc(II) complex was obtained by the reaction of a warm methanolic solution of aamp with a mixture of zinc(II) nitrate and ammonium thiocyanate, whereas the mercury(II) complex was prepared by the reaction of a warm ethanolic solution of aamp and a warm, slightly acidified...

  5. Accelerated corrosion of stainless steel in thiocyanate-containing solutions

    Energy Technology Data Exchange (ETDEWEB)

    Pistorius, P Chris; Li, Wen

    2012-09-19

    It is known that reduced sulfur compounds (such as thiocyanate and thiosulfate) can accelerate active corrosion of austenitic stainless steel in acid solutions, but before we started this project the mechanism of acceleration was largely unclear. This work combined electrochemical measurements and analysis using scanning electron microscopy (SEM) and X-ray photo-electron spectroscopy (XPS), which provided a comprehensive understanding of the catalytic effect of reduced sulfur species on the active corrosion of stainless steel. Both the behavior of the pure elements and the steel were studied and the work focused on the interaction between the pure elements of the steel, which is the least understood area. Upon completion of this work, several aspects are now much clearer. The main results from this work can be summarized as follows: The presence of low concentrations (around 0.1 mM) of thiocyanate or tetrathionate in dilute sulfuric acid greatly accelerates the anodic dissolution of chromium and nickel, but has an even stronger effect on stainless steels (iron-chromium-nickel alloys). Electrochemical measurements and surface analyses are in agreement with the suggestion that accelerated dissolution really results from suppressed passivation. Even well below the passivation potential, the electrochemical signature of passivation is evident in the electrode impedance; the electrode impedance shows clearly that this pre-passivation is suppressed in the presence of thiocyanate. For the stainless steels, remarkable changes in the morphology of the corroded metal surface and in the surface concentration of chromium support the suggestion that pre-passivation of stainless steels is suppressed because dissolution of chromium is accelerated. Surface analysis confirmed that adsorbed sulfur / sulfide forms on the metal surfaces upon exposure to solutions containing thiocyanate or thiosulfate. For pure nickel, and steels containing nickel (and residual copper), bulk sulfide

  6. Coordination Chemistry of Homoleptic Actinide(IV)-Thiocyanate Complexes.

    Science.gov (United States)

    Carter, Tyler J; Wilson, Richard E

    2015-10-26

    The synthesis, X-ray crystal structure, vibrational and optical spectroscopy for the eight-coordinate thiocyanate compounds, [Et4 N]4 [Pu(IV) (NCS)8 ], [Et4 N]4 [Th(IV) (NCS)8 ], and [Et4 N]4 [Ce(III) (NCS)7 (H2 O)] are reported. Thiocyanate was found to rapidly reduce plutonium to Pu(III) in acidic solutions (pHcoordination in acetonitrile based on the observation of intense ligand-to-metal charge-transfer bands. Spectroscopic and crystallographic data do not support the interaction of the metal orbitals with the ligand π system, but support an enhanced An(IV) -NCS interaction, as the Lewis acidity of the metal ion increases from Th to Pu.

  7. Thiocyanate concentration in saliva of cystic fibrosis patients.

    Directory of Open Access Journals (Sweden)

    Marek Gacko

    2008-06-01

    Full Text Available Thiocyanates (SCN- are ubiquitous in nature. There are indispensable part of host defense system that act as a substrate for lactoperoxidase (LPO. In our study we present initial data on SCN- concentration in saliva of CF patients in comparison to healthy non-smokers and healthy smokers. 5 ml of saliva was collected from each subject to a sterile tube and thiocyanate concentration was measured in each sample. The results of the measurements are presented on Fig. 1. Mean concentration of SCN- in saliva of CF patients was 0.031 +/- 0.0052 g/l, in healthy non-smokers 0.039 +/- 0.0048 g/l and in healthy smokers 0.048 +/- 0.0161 g/l. The differences between each group were statistically significant. Studies on larger group of patients and probably on different material (BALF or induced sputum should present interesting data complementing the in vitro studies.

  8. Colorimetric determination of niobium in sodium metal with thiocyanate

    International Nuclear Information System (INIS)

    The niobium determination using the spectrophotometric measurement of the thiocyanate complex is applied for the determination of trace amounts of niobium in sodium. The effects of the concentration of the reagents on the absorbance were studied resulting in the optimization of the conditions for the color development of the complex. The procedure is recommended in the range of up to 10 μg niobium, whereby a detection limit of 0.040 μg Nb ml-1 cm-1 is obtained

  9. DBC solvent extraction of U(VI) from thiocyanate medium

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The extraction behavior of uranium(VI) from thiocyanate medium with dibenzo-18-crown-6 (DBC) in nitrobenzene and the effects of alkali cations on the extraction were investigated. The results showed that the uranium (VI) can be effectively extracted in the presence of potassium cation, uranium (VI) is extracted as complex anionic species UO2(SCN)-3, and the stoichiometry of the extracted complex is KUO2(SCN)32DBC(o).

  10. Recent advances in the chemistry of organic thiocyanates.

    Science.gov (United States)

    Castanheiro, Thomas; Suffert, Jean; Donnard, Morgan; Gulea, Mihaela

    2016-02-01

    Organic thiocyanates are important synthetic intermediates to access valuable sulfur-containing compounds. In this review the different methods for their preparation and their synthetic applications will be presented. The literature of the last 15 years will be covered, highlighting selected recent advances in the chemistry of this class of compounds. We hope to offer chemists the tools to have a good grasp of this singular functionality and open the door to further progress in this chemistry.

  11. Coordination Chemistry of Homoleptic Actinide(IV)-Thiocyanate Complexes.

    Science.gov (United States)

    Carter, Tyler J; Wilson, Richard E

    2015-10-26

    The synthesis, X-ray crystal structure, vibrational and optical spectroscopy for the eight-coordinate thiocyanate compounds, [Et4 N]4 [Pu(IV) (NCS)8 ], [Et4 N]4 [Th(IV) (NCS)8 ], and [Et4 N]4 [Ce(III) (NCS)7 (H2 O)] are reported. Thiocyanate was found to rapidly reduce plutonium to Pu(III) in acidic solutions (pHthiocyanate complex [Et4 N]4 [Pu(IV) (NCS)8 ] was crystallized when a large excess of [Et4 N][NCS] was present. This compound, along with its U(IV) analogue, maintains inner-sphere thiocyanate coordination in acetonitrile based on the observation of intense ligand-to-metal charge-transfer bands. Spectroscopic and crystallographic data do not support the interaction of the metal orbitals with the ligand π system, but support an enhanced An(IV) -NCS interaction, as the Lewis acidity of the metal ion increases from Th to Pu. PMID:26493880

  12. Thiocyanate linkage isomerism in a ruthenium polypyridyl complex.

    Science.gov (United States)

    Brewster, Timothy P; Ding, Wendu; Schley, Nathan D; Hazari, Nilay; Batista, Victor S; Crabtree, Robert H

    2011-12-01

    Ruthenium polypyridyl complexes have seen extensive use in solar energy applications. One of the most efficient dye-sensitized solar cells produced to date employs the dye-sensitizer N719, a ruthenium polypyridyl thiocyanate complex. Thiocyanate complexes are typically present as an inseparable mixture of N-bound and S-bound linkage isomers. Here we report the synthesis of a new complex, [Ru(terpy)(tbbpy)SCN][SbF(6)] (terpy = 2,2';6',2''-terpyridine, tbbpy = 4,4'-di-tert-butyl-2,2'-bipyridine), as a mixture of N-bound and S-bound thiocyanate linkage isomers that can be separated based on their relative solubility in ethanol. Both isomers have been characterized spectroscopically and by X-ray crystallography. At elevated temperatures the isomers equilibrate, the product being significantly enriched in the more thermodynamically stable N-bound form. Density functional theory analysis supports our experimental observation that the N-bound isomer is thermodynamically preferred, and provides insight into the isomerization mechanism. PMID:22066656

  13. Bioreactor microbial ecosystems for thiocyanate and cyanide degradation unravelled with genome-resolved metagenomics.

    Science.gov (United States)

    Kantor, Rose S; van Zyl, A Wynand; van Hille, Robert P; Thomas, Brian C; Harrison, Susan T L; Banfield, Jillian F

    2015-12-01

    Gold ore processing uses cyanide (CN(-) ), which often results in large volumes of thiocyanate- (SCN(-) ) contaminated wastewater requiring treatment. Microbial communities can degrade SCN(-) and CN(-) , but little is known about their membership and metabolic potential. Microbial-based remediation strategies will benefit from an ecological understanding of organisms involved in the breakdown of SCN(-) and CN(-) into sulfur, carbon and nitrogen compounds. We performed metagenomic analysis of samples from two laboratory-scale bioreactors used to study SCN(-) and CN(-) degradation. Community analysis revealed the dominance of Thiobacillus spp., whose genomes harbour a previously unreported operon for SCN(-) degradation. Genome-based metabolic predictions suggest that a large portion of each bioreactor community is autotrophic, relying not on molasses in reactor feed but using energy gained from oxidation of sulfur compounds produced during SCN(-) degradation. Heterotrophs, including a bacterium from a previously uncharacterized phylum, compose a smaller portion of the reactor community. Predation by phage and eukaryotes is predicted to affect community dynamics. Genes for ammonium oxidation and denitrification were detected, indicating the potential for nitrogen removal, as required for complete remediation of wastewater. These findings suggest optimization strategies for reactor design, such as improved aerobic/anaerobic partitioning and elimination of organic carbon from reactor feed. PMID:26031303

  14. Bioreactor microbial ecosystems for thiocyanate and cyanide degradation unravelled with genome-resolved metagenomics.

    Science.gov (United States)

    Kantor, Rose S; van Zyl, A Wynand; van Hille, Robert P; Thomas, Brian C; Harrison, Susan T L; Banfield, Jillian F

    2015-12-01

    Gold ore processing uses cyanide (CN(-) ), which often results in large volumes of thiocyanate- (SCN(-) ) contaminated wastewater requiring treatment. Microbial communities can degrade SCN(-) and CN(-) , but little is known about their membership and metabolic potential. Microbial-based remediation strategies will benefit from an ecological understanding of organisms involved in the breakdown of SCN(-) and CN(-) into sulfur, carbon and nitrogen compounds. We performed metagenomic analysis of samples from two laboratory-scale bioreactors used to study SCN(-) and CN(-) degradation. Community analysis revealed the dominance of Thiobacillus spp., whose genomes harbour a previously unreported operon for SCN(-) degradation. Genome-based metabolic predictions suggest that a large portion of each bioreactor community is autotrophic, relying not on molasses in reactor feed but using energy gained from oxidation of sulfur compounds produced during SCN(-) degradation. Heterotrophs, including a bacterium from a previously uncharacterized phylum, compose a smaller portion of the reactor community. Predation by phage and eukaryotes is predicted to affect community dynamics. Genes for ammonium oxidation and denitrification were detected, indicating the potential for nitrogen removal, as required for complete remediation of wastewater. These findings suggest optimization strategies for reactor design, such as improved aerobic/anaerobic partitioning and elimination of organic carbon from reactor feed.

  15. Elevated ammonium levels

    DEFF Research Database (Denmark)

    Søgaard, Rikke; Novak, Ivana; MacAulay, Nanna

    2012-01-01

    Increased ammonium (NH(4)(+)/NH(3)) in the brain is a significant factor in the pathophysiology of hepatic encephalopathy, which involves altered glutamatergic neurotransmission. In glial cell cultures and brain slices, glutamate uptake either decreases or increases following acute ammonium expos...

  16. Investigation of concentration of thiocyanate ion in raw cow's milk from China, New Zealand and the Netherlands.

    Science.gov (United States)

    Yong, Ling; Wang, Yibaina; Yang, Dajin; Liu, Zhaoping; Abernethy, Grant; Li, Jianwen

    2017-01-15

    Thiocyanate ion is a natural component of cow's milk (hereinafter as milk) which may be artificially augmented to activate the lactoperoxidase milk preservation system. This study presents a survey of thiocyanate levels in raw milk and proposes a naturally occurring baseline concentration of thiocyanate in milk, which is the basis for market supervision. 1669 raw milk samples from China, 270 samples from New Zealand and 120 from the Netherlands were collected in the survey. 65% of the samples contained thiocyanate above the detection limit. The average concentration of thiocyanate was 2.11mg/kg (0.10-16.20mg/kg). Differences in the concentrations of thiocyanate were found among three countries, the 12 selected provinces in China, and between summer and winter. The baseline concentration of thiocyanate found in raw cow's milk was statistically calculated and rounded to 9.0mg/kg. Thiocyanate in milk at this level does not present a food safety concern. PMID:27542450

  17. Infrared Spectroscopic Analysis of Linkage Isomerism in Metal-Thiocyanate Complexes

    Science.gov (United States)

    Baer, Carl; Pike, Jay

    2010-01-01

    We developed an experiment suitable for an advanced inorganic chemistry laboratory that utilizes a cooperative learning environment, which allows students to develop an empirical method of determining the bonding mode of a series of unknown metal-thiocyanate complexes. Students synthesize the metal-thiocyanate complexes and obtain the FT-IR…

  18. Thiocyanate in food and iodine in milk: From domestic animal feeding to improved understanding of cretinism

    DEFF Research Database (Denmark)

    Laurberg, P.; Andersen, S.; Knudsen, N.;

    2002-01-01

    the iodine content of consumer milk, and this may influence the risk of thyroid diseases in the population. Thiocyanate inhibition of iodine transport into milk may also be operative in humans with a high thiocyanate intake. This could further impair iodine status in breastfed children in low-iodine intake...

  19. CuI-catalyzed Synthesis of Aryl Thiocyanates from Aryl Iodides

    Institute of Scientific and Technical Information of China (English)

    Ye Feng WANG; Yuan ZHOU; Jia Rui WANG; Lei LIU; Qing Xiang GUO

    2006-01-01

    An operationally simple and inexpensive catalyst system was developed for the cross coupling of potassium thiocyanate with aryl iodides by using CuI as catalyst, 1, 10-phenanthroline as ligand, and tetraethylammonium iodide as activator. The procedure is applicable for the synthesis of diverse aryl thiocyanates without any exotic, poisonous reagents.

  20. Structural and mechanical studies of cadmium manganese thiocyanate crystal

    Science.gov (United States)

    Manikandan, M. R.; Vijayaprasath, G.; babu, G. Anandha; Bhagavannarayan, G.; Vijayan, N.; Ravi, G.

    2012-06-01

    Single crystals of cadmium manganese thiocyanate (CMTC) have been synthesized successfully and grown by slow evaporation method. The structural perfection of the grown crystals has been analyzed by High resolution X-ray diffraction (HRXRD), which shows the crystalline perfection of the grown crystal is quite good. Optical behavior was assessed by UV-Vis analysis and found that no absorption in the UV visible region and it may be useful for second harmonic applications. The mechanical hardness of the grown crystals was studied and Vicker's microhardness, Stiffness constant was calculated.

  1. 2-(Pyridin-2-ylamino)pyridinium thiocyanate acetonitrile monosolvate

    OpenAIRE

    Bonell Schmitt; Thomas Gerber; Eric Hosten; Richard Betz

    2011-01-01

    The title compound, C10H10N3+·NCS−·CH3CN, is the acetonitrile solvate of the thiocyanate salt of protonated dipyridin-2-ylamine. Protonation occurs at one of the pyridine N atoms. The molecular geometry around the central N atom is essentially planar (sum of angles = 359.89°). In the crystal, N—H...N hydrogen bonds, as well as C—H...S contacts link the different residues into chains along the c-axis direction. Interaction between aromat...

  2. Growth and characterization of cadmium magnesium tetra thiocyanate crystals

    Energy Technology Data Exchange (ETDEWEB)

    Gunasekaran, S. [Post Graduate and Research Department of Physics, Pachaiyappa' s College, Chennai - 600 030 (India); Ponnusamy, S. [Department of Physics, S. R. M. Institute of Science and Technology, Kattankulathur - 603 203 (India)

    2006-02-01

    Cadmium Magnesium Tetra Thiocyanate, CdMg(SCN){sub 4}, [CMTC] belongs to bimetallic thiocyanate complexes. CMTC crystals has been grown by solution growth technique at room temperature. The morphologies of the grown crystals are identified by single crystal analysis. Also the Powder X-ray Diffractogram of the crystal has been recorded and the various planes of reflection are identified. The title compound crystallizes under triclinic structure with lattice parameters a=10.0976 Aa, b=7.5015 Aa, c=5.7720 Aa and {beta}=90.2135 . The presence of magnesium and cadmium in the grown crystals were confirmed through Atomic Absorption Spectroscopy. The grown crystals are analysed qualitatively by Fourier Transform Infrared (FTIR) and Fourier Transform Raman spectral measurements. The transmittance spectrum of the crystal in the UV-Visible region has been recorded and analysed. The dielectric measurements for the crystals were carried out in the microwave region. The thermal stabilities of the crystals were studied by using different thermal analyses like Thermo Gravimetric Analysis (TGA), Differential Thermal Analysis (DTA) and Differential Scanning Calorimetry (DSC). (copyright 2006 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  3. Anion-exchange separations of metal ions in thiocyanate media.

    Science.gov (United States)

    Fritz, J S; Kaminski, E E

    1971-05-01

    The analytical potential of a weak-base macroreticular anion-exchange resin for the quantitative separation of metal ions in thiocyanate media is investigated and demonstrated. Distribution data are given for the sorption of some 25 metal ions from aqueous mixtures of potassium thiocyanate (1.0M or less) and 0.5M hydrochloric acid. The magnitude of the distribution data suggests many possible separations, some of which were quantitatively performed by procedures which are fast, simple and require only mild conditions. Representative separations are removal of traces of iron(III) and copper(II) from water samples prior to the determination of water hardness (calcium and magnesium), separation of nickel(II) from vanadium(IV) and the separation of thorium(IV) from titanium(IV). Some multicomponent separations are the separation of rare earths(III) and thorium(IV) from scandium(III) and the separation of rare earths(III) from iron(III) and uranium(VI). PMID:18960914

  4. Binding of thiocyanate to lactoperoxidase: 1H and 15N nuclear magnetic resonance studies

    Energy Technology Data Exchange (ETDEWEB)

    Modi, S.; Behere, D.V.; Mitra, S. (Tata Institute of Fundamental Research, Bombay (India))

    1989-05-30

    The binding of thiocyanate to lactoperoxidase (LPO) has been investigated by 1H and 15N NMR spectroscopy. 1H NMR of LPO shows that the major broad heme methyl proton resonance at about 61 ppm is shifted upfield by addition of the thiocyanate, indicating binding of the thiocyanate to the enzyme. The pH dependence of line width of 15N resonance of SC15N- in the presence of the enzyme has revealed that the binding of the thiocyanate to the enzyme is facilitated by protonation of an ionizable group (with pKa of 6.4), which is presumably distal histidine. Dissociation constants (KD) of SC15N-/LPO, SC15N-/LPO/I-, and SC15N-/LPO/CN- equilibria have been determined by 15N T1 measurements and found to be 90 +/- 5, 173 +/- 20, and 83 +/- 6 mM, respectively. On the basis of these values of KD, it is suggested that the iodide ion inhibits the binding of the thiocyanate but cyanide ion does not. The thiocyanate is shown to bind at the same site of LPO as iodide does, but the binding is considerably weaker and is away from the ferric ion. The distance of 15N of the bound thiocyanate ion from the iron is determined to be 7.2 +/- 0.2 A from the 15N T1 measurements.

  5. Synthesis, growth and characterization of cadmium manganese thiocyanate (CMTC) crystal

    Science.gov (United States)

    Paramasivam, P.; Raja, C. Ramachandra

    2011-09-01

    Single crystals of cadmium manganese thiocyanate, CdMn(SCN)4 (CMTC) have been successfully synthesized and grown by slow evaporation solution growth technique using water as solvent at room temperature. The crystal was characterized by different techniques for finding its suitability for device fabrications. From the single crystal XRD the crystal system was identified as tetragonal. The functional groups were identified from FTIR analysis. The optical studies have been carried out and found that the tendency of transmission observed from the specimen with respect to the wavelength of light is practically more suitable for the present trends in communication engineering. From the thermal analysis the decomposing temperature of the grown crystal is more significant when compared with the studies performed earlier.

  6. Uric acid and thiocyanate as competing substrates of lactoperoxidase.

    Science.gov (United States)

    Seidel, Antonia; Parker, Heather; Turner, Rufus; Dickerhof, Nina; Khalilova, Irada S; Wilbanks, Sigurd M; Kettle, Anthony J; Jameson, Guy N L

    2014-08-01

    The physiological function of urate is poorly understood. It may act as a danger signal, an antioxidant, or a substrate for heme peroxidases. Whether it reacts sufficiently rapidly with lactoperoxidase (LPO) to act as a physiological substrate remains unknown. LPO is a mammalian peroxidase that plays a key role in the innate immune defense by oxidizing thiocyanate to the bactericidal and fungicidal agent hypothiocyanite. We now demonstrate that urate is a good substrate for bovine LPO. Urate was oxidized by LPO to produce the electrophilic intermediates dehydrourate and 5-hydroxyisourate, which decayed to allantoin. In the presence of superoxide, high yields of hydroperoxides were formed by LPO and urate. Using stopped-flow spectroscopy, we determined rate constants for the reaction of urate with compound I (k1 = 1.1 × 10(7) M(-1) s(-1)) and compound II (k2 = 8.5 × 10(3) M(-1) s(-1)). During urate oxidation, LPO was diverted from its peroxidase cycle because hydrogen peroxide reacted with compound II to give compound III. At physiologically relevant concentrations, urate competed effectively with thiocyanate, the main substrate of LPO for oxidation, and inhibited production of hypothiocyanite. Similarly, hypothiocyanite-dependent killing of Pseudomonas aeruginosa was inhibited by urate. Allantoin was present in human saliva and associated with the concentration of LPO. When hydrogen peroxide was added to saliva, oxidation of urate was dependent on its concentration and peroxidase activity. Our findings establish urate as a likely physiological substrate for LPO that will influence host defense and give rise to reactive electrophilic metabolites.

  7. New insights into the genetic and metabolic diversity of thiocyanate-degrading microbial consortia.

    Science.gov (United States)

    Watts, Mathew P; Moreau, John W

    2016-02-01

    Thiocyanate is a common contaminant of the gold mining and coal coking industries for which biological degradation generally represents the most viable approach to remediation. Recent studies of thiocyanate-degrading bioreactor systems have revealed new information on the structure and metabolic activity of thiocyanate-degrading microbial consortia. Previous knowledge was limited primarily to pure-culture or co-culture studies in which the effects of linked carbon, sulfur and nitrogen cycling could not be fully understood. High throughput sequencing, DNA fingerprinting and targeted gene amplification have now elucidated the genetic and metabolic diversity of these complex microbial consortia. Specifically, this has highlighted the roles of key consortium members involved in sulfur oxidation and nitrification. New insights into the biogeochemical cycling of sulfur and nitrogen in bioreactor systems allow tailoring of the microbial metabolism towards meeting effluent composition requirements. Here we review these rapidly advancing studies and synthesize a conceptual model to inform new biotechnologies for thiocyanate remediation. PMID:26596573

  8. Unique stress response to the lactoperoxidase-thiocyanate enzyme system in Escherichia coli.

    Science.gov (United States)

    Sermon, Jan; Vanoirbeek, Kristof; De Spiegeleer, Philipp; Van Houdt, Rob; Aertsen, Abram; Michiels, Chris W

    2005-03-01

    Using a differential fluorescence induction approach, we screened a promoter trap library constructed in a vector with a promoterless gfp gene for Escherichia coli MG1655 promoters that are induced upon challenge with the antimicrobial lactoperoxidase-thiocyanate enzyme system. None of the thirteen identified lactoperoxidase-inducible open reading frames was inducible by H(2)O(2) or by the superoxide generator plumbagin. However, analysis of specific promoters of known stress genes showed some of these, including recA, dnaK and sodA, to be inducible by the lactoperoxidase-thiocyanate enzyme system. The results show that the lactoperoxidase-thiocyanate enzyme system elicits a distinct stress response different from but partly overlapping other oxidative stress responses. Several of the induced genes or pathways may be involved in bacterial defense against the toxic effects of the lactoperoxidase-thiocyanate enzyme system.

  9. Repairing of low-temperature induced injury in rice seedlings by thiourea, cystine and potassium thiocyanate

    International Nuclear Information System (INIS)

    The effect of low temperature treatment of seeds of Satika var. of rice (parent and mutant) either singly or in combination with chemicals viz., thiourea, cystine and potassium thiocyanate on germination, growth and radiophosphorus uptake behaviour of the seedlings has been investigated. Results show that inhibition of germination, growth and P32 uptake caused by low temperature is distinctly repaired by treatment with thiourea and to some extent by cystine and potassium thiocyanate. (M.G.B.)

  10. Adamantane-1-ammonium acetate

    Directory of Open Access Journals (Sweden)

    Elise J. C. de Vries

    2011-06-01

    Full Text Available In the title compound, C10H18N+·C2H3O2−, the ammonium H atoms of the cation are linked to three acetate anions via N—H...O hydrogen bonds, forming a chain structure extending along the b axis.

  11. Analysis of radiolabelled thiocyanate tracer in oil field brines

    International Nuclear Information System (INIS)

    Thiocyanate (SCN-) labelled with 14C or 35S is applicable for the tracing of the water flow in water-driven oil production. This work describes two improved methods for increasing the concentration of S14CN- with sample sizes up to 1000 ml of sampled brine. The radioactivity detection is carried out by low-background liquid scintillation counting using standard-size counting vials of 20 ml. The first method is based on solvent extraction: two extraction/strip steps reduce the volume by the required factor of 100 down to 10 ml. The extraction agent is 0.5M tri-isooctylamine (TiOA) in Solvesso-150 and the stripping agent is 5M NH3. A chemical yield of 70-75%, a somewhat unfavourable quenching factor and a moderate reproducibility lead to a detection limit LD of 0.04 Bq/1. The second method is based on anion exchange. 1000 ml tracer-containing brine may be loaded onto 6.1 ml of the anion-exchange resin AG1-x8 before significant breakthrough of the tracer. More than 98.4% is absorbed. By elution with 2.8M sodiumperchlorate, more than 99.5% of the absorbed tracer is concentrated in a sharp elution peak of 10 ml. With a total chemical yield of 98%, a lower quenching factor and higher reproducibility than for the solvent extraction method, an LD-value of 0.005 Bq/1 is obtained. (orig.)

  12. [Determination of iodide, thiocyanate and perchlorate ions in environmental water by two-dimensional ion chromatography].

    Science.gov (United States)

    Lin, Li; Wang, Haibo; Shi, Yali

    2013-03-01

    A procedure for the determination of iodide, thiocyanate and perchlorate ions in environmental water by two-dimensional ion chromatography has been developed. At first the iodide, thiocyanate and perchlorate ions were separated from interfering ions by a column (IonPac AS16, 250 mm x 4 mm). The iodide ion, thiocyanate and perchlorate ions were then enriched with an enrichment column (MAC-200, 80 mm x 0.75 mm). In the 2nd-dimensional chromatography, iodide thiocyanate and perchlorate ions were separated and quantified by a capillary column (IonPac AS20 Capillary, 250 mm x 0.4 mm). The linear ranges were 0.05 -100 pg/L with correlation coefficients of 0. 999 9, and the detection limits were 0. 02 - 0.05 micro gg/L. The spiked recoveries of iodide, thiocyanate and perchlorate ions were in the range of 85.1% to 100.1%. The relative standard deviations of the recoveries were 1.7% to 4.9%.

  13. Structural, spectral and mechanical studies of bimetallic crystal: cadmium manganese thiocyanate single crystals

    Science.gov (United States)

    Manikandan, M.; Vijaya Prasath, G.; Bhagavannarayan, G.; Vijayan, N.; Mahalingam, T.; Ravi, G.

    2012-09-01

    A nonlinear optical bimetallic thiocyanate complex crystal, cadmium manganese thiocyanate (CMTC) has been successfully synthesized. The growth of single crystals of cadmium manganese thiocyanate has been accomplished from aqueous solution using slow evaporation method. The presence of manganese and cadmium in the synthesized material was confirmed through energy dispersive spectrum (EDS) analysis. Structural analysis was carried out using powder X-ray diffractometer (PXRD) and crystalline perfection of the grown crystals was ascertained by high-resolution X-ray diffraction (HRXRD) analysis. Fourier transform infrared (FTIR) spectrum was taken to confirm the functional groups. The transmittance spectrum of the crystal in the UV-visible region has been recorded and the cutoff wavelength has been determined. The dielectric measurements for the crystals were performed for various frequencies and temperatures. The mechanical properties were evaluated by Vickers microhardness testing, which reveals hardness and stiffness constant of the crystals.

  14. Structural, spectral and mechanical studies of bimetallic crystal: cadmium manganese thiocyanate single crystals

    Energy Technology Data Exchange (ETDEWEB)

    Manikandan, M.; Vijaya Prasath, G.; Mahalingam, T.; Ravi, G. [Alagappa University, Department of Physics, Karaikudi (India); Bhagavannarayan, G.; Vijayan, N. [National Physical Laboratory, Materials Characterization Division, New Delhi (India)

    2012-09-15

    A nonlinear optical bimetallic thiocyanate complex crystal, cadmium manganese thiocyanate (CMTC) has been successfully synthesized. The growth of single crystals of cadmium manganese thiocyanate has been accomplished from aqueous solution using slow evaporation method. The presence of manganese and cadmium in the synthesized material was confirmed through energy dispersive spectrum (EDS) analysis. Structural analysis was carried out using powder X-ray diffractometer (PXRD) and crystalline perfection of the grown crystals was ascertained by high-resolution X-ray diffraction (HRXRD) analysis. Fourier transform infrared (FTIR) spectrum was taken to confirm the functional groups. The transmittance spectrum of the crystal in the UV-visible region has been recorded and the cutoff wavelength has been determined. The dielectric measurements for the crystals were performed for various frequencies and temperatures. The mechanical properties were evaluated by Vickers microhardness testing, which reveals hardness and stiffness constant of the crystals. (orig.)

  15. A two-dimensional cadmium(II) polymer based on nicotinic acid and thiocyanate ligands.

    Science.gov (United States)

    Zhou, Lin; Wang, Hui-Ting

    2015-09-01

    A cadmium-thiocyanate complex, poly[[bis(nicotinic acid-κN)di-μ-thiocyanato-κ(2)N:S;κ(2)S:N-cadmium(II)] monohydrate], {[Cd(NCS)2(C6H5NO2)2]·H2O}n, was synthesized by the reaction of nicotinic acid, cadmium nitrate tetrahydrate and potassium thiocyanide in aqueous solution. In the crystal structure, each Cd(II) cation is in a distorted octahedral coordination environment, coordinated by the N and S atoms of nicotinic acid and thiocyanate ligands. Neighbouring Cd(II) cations are linked together by thiocyanate bridges to form a two-dimensional network. Hydrogen-bond interactions between the uncoordinated solvent water molecules and the organic ligands result in the formation of the three-dimensional supramolecular network. PMID:26322616

  16. Catalytic wet oxidation of thiocyanate with homogeneous copper(II) sulphate catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Collado, Sergio; Laca, Adriana [Department of Chemical Engineering and Environmental Technology, University of Oviedo, c/ Julian Claveria s/n, E-33071, Oviedo (Spain); Diaz, Mario, E-mail: mariodiaz@uniovi.es [Department of Chemical Engineering and Environmental Technology, University of Oviedo, c/ Julian Claveria s/n, E-33071, Oviedo (Spain)

    2010-05-15

    The wet oxidation of thiocyanate has been investigated in a semi-batch reactor at temperatures between 423 and 473 K and pressures between 6.1 x 10{sup 3} and 1.0 x 10{sup 4} kPa in the presence of copper(II) sulphate as catalyst. The effects of copper concentration, initial thiocyanate concentration, pressure and temperature on the reaction rate were analyzed and the main products of reaction were identified. A kinetic model for the Cu-catalyzed reaction is here proposed, including temperature, oxygen concentration, and the reduction of Cu{sup 2+} to Cu{sup +} that gives an accurate prediction of the oxidation process under the assayed conditions. A mechanistic model based on the formation of a transition complex between a copper cation and two thiocyanate anions has been proposed for the catalytic wet oxidation.

  17. Catalytic wet oxidation of thiocyanate with homogeneous copper(II) sulphate catalyst.

    Science.gov (United States)

    Collado, Sergio; Laca, Adriana; Díaz, Mario

    2010-05-15

    The wet oxidation of thiocyanate has been investigated in a semi-batch reactor at temperatures between 423 and 473 K and pressures between 6.1 x 10(3) and 1.0 x 10(4)kPa in the presence of copper(II) sulphate as catalyst. The effects of copper concentration, initial thiocyanate concentration, pressure and temperature on the reaction rate were analyzed and the main products of reaction were identified. A kinetic model for the Cu-catalyzed reaction is here proposed, including temperature, oxygen concentration, and the reduction of Cu(2+) to Cu(+) that gives an accurate prediction of the oxidation process under the assayed conditions. A mechanistic model based on the formation of a transition complex between a copper cation and two thiocyanate anions has been proposed for the catalytic wet oxidation.

  18. Synthesis, optical and dielectric properties of highly efficient organobimetallic thiocyanate complex crystals

    Science.gov (United States)

    R, Santhosh Kumar; Chandralingam, S.; Augustine, Anju K.; G, Sreekanth; Joseph, Ginson P.

    2013-05-01

    Single crystals of Manganese Mercury Thiocyanate (MMTC) and its lewis base adduct Manganese Mercury Thiocyanate bis dimethyl sulfoxide (MMTD) have been grown by low temperature solution growth technique. Piezoelectric charge coefficient (d33 pC/N) of MMTC and MMTD at 110 Hz was found to be 3 pC/N and 8 pC/N respectively. Hysteresis loop parameters such as remnant polarization (Pr) and coercive field (Ec) of grown samples were also determined. The mechanical behaviors of the samples were studied using Leitz Weitzler hardness tester. The band gap of the samples was also measured.

  19. Is Cytox 3522 (10% methylene-bis-thiocyanate) a human skin sensitizer?

    DEFF Research Database (Denmark)

    Andersen, Klaus Ejner; Hamann, K

    1983-01-01

    Methylene-bis-thiocyanate is an antimicrobial agent in Cytox 3522 (American Cyanamid Corporation) and Nalco 206 (Nalco Chemical Company). Both are wide-spectrum industrial biocides. Cytox 3522 showed a strong sensitization potential in guineau pigs using the Guinea Pig Maximization Test and the O......Methylene-bis-thiocyanate is an antimicrobial agent in Cytox 3522 (American Cyanamid Corporation) and Nalco 206 (Nalco Chemical Company). Both are wide-spectrum industrial biocides. Cytox 3522 showed a strong sensitization potential in guineau pigs using the Guinea Pig Maximization Test...

  20. 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.

  1. Comment on the paper: Synthesis, growth and characterization of cadmium manganese thiocyanate (CMTC) crystal

    OpenAIRE

    Srinivasan, Bikshandarkoil R.

    2015-01-01

    The authors of the title paper (Spectrochim. Acta 79A (2011) 340-343) report the crystal growth of cadmium manganese thiocyanate CdMn(SCN)4 and its characterization by single crystal X-ray diffraction and infrared spectrum. Many points of criticism, concerning the crystal growth and reported experimental data are highlighted in this report.

  2. Thermochromism and switchable paramagnetism of cobalt(II) in thiocyanate ionic liquids.

    Science.gov (United States)

    Osborne, Stephen J; Wellens, Sil; Ward, Chris; Felton, Solveig; Bowman, Robert M; Binnemans, Koen; Swadźba-Kwaśny, Małgorzata; Gunaratne, H Q Nimal; Nockemann, Peter

    2015-07-01

    Temperature-dependent switching of paramagnetism of a cobalt(II) complex is observed in an ionic liquid solution. Paramagnetic and thermochromic switching occur simultaneously due to a reversible change in coordination. This reversible switching is possible in the ionic liquid solution, which enables mobility of thiocyanate anions by remaining mobile at low temperatures and acts as an anion reservoir. PMID:26053484

  3. Thermochromism and switchable paramagnetism of cobalt(ii) in thiocyanate ionic liquids

    OpenAIRE

    Osborne, Stephen J; Wellens, Sil; Ward, Chris; Felton, Solveig; Bowman, Robert M.; Binnemans, Koen; Swadźba-Kwaśny, Małgorzata; Gunaratne, H. Q. Nimal; Nockemann, Peter

    2015-01-01

    Temperature-dependent switching of paramagnetism of a cobalt(ii) complex is observed in an ionic liquid solution. Paramagnetic and thermochromic switching occur simultaneously due to a reversible change in coordination. This reversible switching is possible in the ionic liquid solution, which enables mobility of thiocyanate anions by remaining mobile at low temperatures and acts as an anion reservoir.

  4. Simultaneous oxidation of cyanide and thiocyanate at high pressure and temperature

    Energy Technology Data Exchange (ETDEWEB)

    Oulego, Paula; Collado, Sergio; Laca, Adriana; Díaz, Mario, E-mail: mariodiaz@uniovi.es

    2014-09-15

    Graphical abstract: - Highlights: • The oxidation rate of SCN{sup −} was greatly enhanced by the presence of CN{sup −}. • The degradation of mixtures was significantly affected by temperature and pressure. • A free-radical pathway was proposed, CN{sup −} and CNO{sup −} being the reaction intermediates. • The principal reaction products were found to be HCOO{sup −}, NH{sub 3} and SO{sub 4}{sup 2−}. • One of the parallel routes gives the found products and the other N{sub 2}, CO{sub 2} and H{sub 2}. - Abstract: Thiocyanate and cyanide are important contaminants that frequently appear mixed in industrial effluents. In this work the wet oxidation of mixtures of both compounds, simulating real compositions, was carried out in a semi-batch reactor at temperature between 393 K and 483 K and pressure in the range of 2.0–8.0 MPa. The presence of cyanide (3.85 mM) increased the kinetic constant of thiocyanate degradation by a factor of 1.6, in comparison to the value obtained for the individual degradation of thiocyanate, (5.95 ± 0.05) × 10{sup −5} s{sup −1}. On the other hand, the addition of thiocyanate (0.98 mM) decreased the degradation rate of cyanide by 16%. This revealed the existence of synergistic and inhibitory phenomena between these two species. Additionally, cyanide was identified as an intermediate in the oxidation of thiocyanate, and formate, ammonia and sulfate were found to be the main reaction products. Taking into account the experimental data, a reaction pathway for the simultaneous wet oxidation of both pollutants was proposed. Two parallel reactions beginning from cyanate as intermediate were considered, one yielding ammonia and formate and the other giving carbon dioxide and nitrogen as final products.

  5. A practical synthesis of 3,4-diethoxybenzthioamide based on Friedel-Crafts reaction with potassium thiocyanate in methanesulfonic acid.

    Science.gov (United States)

    Aki, Shinji; Fujioka, Takafumi; Ishigami, Masashi; Minamikawa, Jun-ichi

    2002-09-01

    The synthesis of 3,4-diethoxybenzthioamide, the key intermediate for OPC-6535, is achieved by employing Friedel-Crafts reaction of 1,2-diethoxybenzene with potassium thiocyanate in methanesulfonic acid at ambient temperature.

  6. Antibacterial activity of hydrogen peroxide and the lactoperoxidase-hydrogen peroxide-thiocyanate system against oral streptococci.

    OpenAIRE

    Thomas, E L; Milligan, T W; Joyner, R E; Jefferson, M M

    1994-01-01

    In secreted fluids, the enzyme lactoperoxidase (LP) catalyzes the oxidation of thiocyanate ion (SCN-) by hydrogen peroxide (H2O2), producing the weak oxidizing agent hypothiocyanite (OSCN-), which has bacteriostatic activity. However, H2O2 has antibacterial activity in the absence of LP and thiocyanate (SCN-). Therefore, LP may increase antibacterial activity by using H2O2 to produce a more effective inhibitor of bacterial metabolism and growth, or LP may protect bacteria against the toxicity...

  7. Lactoperoxidase-catalyzed oxidation of thiocyanate by hydrogen peroxide: sup 15 N nuclear magnetic resonance and optical spectral studies

    Energy Technology Data Exchange (ETDEWEB)

    Modi, S.; Deodhar, S.S.; Behere, D.V.; Mitra, S. (Tata Institute of Fundamental Research, Bombay (India))

    1991-01-01

    To establish the agent(s) responsible for the activity of the lactoperoxidase (LPO)/SCN{sup {minus}}/H{sub 2}O{sub 2} system, the oxidation of thiocyanate with hydrogen peroxide, catalyzed by lactoperoxidase, has been studied by {sup 15}N NMR and optical spectroscopy at different concentrations of thiocyanate and hydrogen peroxide and at different pHs. The formation of hypothiocyanite ion (OSCN{sup {minus}}) as one of the oxidation products correlated well with activity of the LPO/SCN{sup {minus}}/H{sub 2}O{sub 2} system and was maximum when the concentrations of the H{sub 2}O{sub 2} and SCN{sup {minus}} were nearly the same and the pH was <6.0. At (H{sub 2}O{sub 2})/(SCN{sup {minus}}) = 1, OSCN{sup {minus}} decomposed very slowly back to thiocyanate. When the ratio (H{sub 2}O{sub 2})/(SCN{sup {minus}}) was above 2, formation of CN{sup {minus}} was observed, which was confirmed by {sup 15}N NMR and also by changes in the optical spectrum of LPO. The oxidation of thiocyanate by H{sub 2}O{sub 2} in the presence of LPO does not take place at pH >8.0. Since thiocyanate does not bind to LPO above this pH, the binding of thiocyanate to LPO is considered to be prerequisite for the oxidation of thiocyanate. Maximum inhibition of oxygen uptake by Streptococcus cremoris 972 bacteria was observed when hydrogen peroxide and thiocyanate were present in equimolar amounts and the pH was below 6.0.

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

    Science.gov (United States)

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

    2016-08-18

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

  9. Chloroform Aided Extraction Spectrophotometric Determination of Rhenium Using Thiocyanate Complexing Agent

    Institute of Scientific and Technical Information of China (English)

    E. Keshavarz Alamdari; S.K. Sadrnezhaad; Z. Mos-hefi Shabestari

    2005-01-01

    A new technique is developed for quantitative determination of rhenium in aqueous media containing molybdenum,iron and copper ions. The method seems easier and more accurate than the traditional ones. It consists of the formation of rhenium thiocyanate complex, which is extracted with chloroform at the presence of hydrochloric acid.This complex is a highly visible light absorbent that can easily be detected with the aid of a spectrophotometer. The maximum absorbance (λmax) observed for this complex was in the visible range of 430~435 nm. The experimental results showed that in a concentration range from 0.5~8 mg/L, the absorbance behavior of the rhenium thiocyanate complex is followed to the Beer-Lambert law.

  10. A solvent extraction study of molybdenum chloride and molybdenum thiocyanate complexes

    Science.gov (United States)

    Greenland, L.P.; Lillie, E.G.

    1974-01-01

    The effect of reducing agents on molybdenum(VI) solutions in hydrochloric acid was studied by a solvent extraction technique to elucidate the composition of the colored molybdenum thiocyanate complex. Neither copper(I) chloride nor ascorbic acid have any effect on the extraction of MoO2Cl2; it is inferred that tin(II) chloride reduces Mo(VI) stepwise to a polynuclear Mo(V)??Mo(VI) complex and then to Mo(V). The colored thiocyanate complex produced by copper(I) and by ascorbic acid differs only slightly in extraction characteristics from the uncolored Mo(VI) complex. It is suggested that the color may be produced by an isomerization reaction of MoO2(SCN)2, and thus that the colored species may be a hexavalent rather than pentavalent molybdenum complex. ?? 1974.

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

    Science.gov (United States)

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

    2008-05-22

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

  12. GROWTH MODES AND DEFECTS OF MANGANESE MERCURY THIOCYANATE CRYSTALS OBSERVED BY AFM

    OpenAIRE

    Y. L. GENG; Sun, Z. H.

    2009-01-01

    Growth mechanisms and defects formation of the manganese mercury thiocyanate (MMTC) crystal have been investigated by atomic force microscopy (AFM). Both screw dislocation controlled growth and 2D nucleation growth occur on the {110} faces. Stacking faults are observed among dislocation hillocks and the formation of them probably results from the different crystallization orientations of different spirals. Hollow channels are found around the nucleation islands and the formation of them is du...

  13. Research data supporting "Extending motifs in lithiocuprate chemistry: unexpected structural diversity in thiocyanate complexes"

    OpenAIRE

    Peel, Andrew J.; Hedidi, Madani; Ghenia, Bentabed-Ababsa; Thierry, Roisnel; Mongin, Florence; Wheatley, Andrew E. H.

    2015-01-01

    Supporting data for the publication "Extending motifs in lithiocuprate chemistry: unexpected structural diversity in thiocyanate complexes". Single crystal X-ray diffraction structures and NMR spectroscopic data for complexes 8-11 in the paper. All four complexes were made at Cambridge in 2015 and were characterized in house in 2015. NMR spectra for compounds 15 and 16. These were made and characterized in Rennes in 2015.

  14. Development of four-stage moving bed biofilm reactor train with a pre-denitrification configuration for the removal of thiocyanate and cyanate.

    Science.gov (United States)

    Villemur, Richard; Juteau, Pierre; Bougie, Veronique; Ménard, Julie; Déziel, Eric

    2015-04-01

    Two trains (A and B) of four-stage moving bed biofilm reactors (MBBRs) were developed for the degradation of thiocyanate (SCN(-)), cyanate (OCN(-)) and ammonia (NH3). A pre-denitrification configuration was established in the first-stage reactor of the B train using SCN(-) and OCN(-) as the sole carbon source. SCN(-), OCN(-) and NH3 were completely removed in both trains. The highest removal of total nitrogen equivalent (total-N) occurred at a loading rate of 5.6 mg-N L(-1) h(-1). The pre-denitrification configuration resulted in increased total-N removal in the B train (62.6%) compared to the A train (38.5%). Thiobacillus spp. were the predominant bacteria in all MBBRs. Bacteria related to bioprocesses involving anaerobic ammonium oxidation were present in the B train, suggesting that part of nitrogen removal occurs via this pathway. Our results showed that the pre-denitrification configuration increases the efficiency of removal of total-N compounds in the SCN(-)/OCN(-)-degrading MBBR process.

  15. Effect of lactoperoxidase on the antimicrobial effectiveness of the thiocyanate hydrogen peroxide combination in a quantitative suspension test

    Directory of Open Access Journals (Sweden)

    Schwahn Ch

    2009-07-01

    Full Text Available Abstract Background The positive antimicrobial effects of increasing concentrations of thiocyanate (SCN- and H2O2 on the human peroxidase defence system are well known. However, little is known about the quantitative efficacy of the human peroxidase thiocyanate H2O2 system regarding Streptococcus mutans and sanguinis, as well as Candida albicans. The aim of this study was to evaluate the effect of the enzyme lactoperoxidase on the bactericidal and fungicidal effectiveness of a thiocyanate-H2O2 combination above the physiological saliva level. To evaluate the optimal effectiveness curve, the exposure times were restricted to 1, 3, 5, and 15 min. Results The bactericidal and fungicidal effects of lactoperoxidase on Streptococcus mutans and sanguinis and Candida albicans were evaluated by using two test mixtures of a 2.0% (w/v; 0.34 M thiocyanate and 0.4% (w/v; 0.12 M hydrogen peroxide solution, one without and one with lactoperoxidase. Following the quantitative suspension tests (EN 1040 and EN 1275, the growth of surviving bacteria and fungi in a nutrient broth was measured. The reduction factor in the suspension test without lactoperoxidase enzyme was Conclusion The tested thiocyanate and H2O2 mixtures showed no relevant antimicrobial effect. However, by adding lactoperoxidase enzyme, the mixtures became not only an effective bactericidal (Streptococcus mutans and sanguinis but also a fungicidal (Candida albicans agent.

  16. 21 CFR 582.1141 - Ammonium phosphate.

    Science.gov (United States)

    2010-04-01

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

  17. 77 FR 50613 - Didecyl Dimethyl Ammonium Carbonate and Didecyl Dimethyl Ammonium Bicarbonate; Exemption From the...

    Science.gov (United States)

    2012-08-22

    ... AGENCY 40 CFR Part 180 Didecyl Dimethyl Ammonium Carbonate and Didecyl Dimethyl Ammonium Bicarbonate... Didecyl Dimethyl Ammonium Carbonate and Didecyl Dimethyl Ammonium Bicarbonate, jointly referred to as.... Background and Statutory Findings In the Federal Register of December 8, 2011 (76 FR 76674) (FRL-...

  18. Phase diagram of ammonium nitrate

    Science.gov (United States)

    Dunuwille, M.; Yoo, C. S.

    2014-05-01

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

  19. Phase diagram of ammonium nitrate

    International Nuclear Information System (INIS)

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

  20. Biodegradation Of Thiocyanate Using Microbial Consortia Cultured From Gold Mine Tailings

    Science.gov (United States)

    Moreau, J. W.; Watts, M. P.; Spurr, L. P.; Vu, H. P.

    2015-12-01

    Some bacteria possess the capability to degrade SCN-; therefore, harnessing this metabolic trait offers a biotechnological remediation strategy for SCN- produced in gold ore processing. A tailings storage facility (TSF) at a gold mine in Victoria, Australia holds large quantities of thiocyanate (SCN-) contaminated mine waste. The surface water in the TSF typically contains SCN- concentrations of >800 mg L-1, and seepage from the facility has contaminated the groundwater at the site. This study aimed to culture SCN-degrading microbes from the TSF, characterize the microbial consortia and test its operational parameters for use in a thiocyanate-degrading bioreactor. Surface samples were obtained from several locations around the TSF facility and used to inoculate medium reflective of the moderately saline and alkaline tailings water at the TSF, in the absence of organic carbon but subject to additions of phosphate and trace metals. Four microbial consortia capable of rapid SCN- degradation were successfully cultured. Sequencing of 16S rRNA genes found that the consortia were dominated by Thiobacillus species, a genus of known SCN- degraders. Lower abundances of other SCN- degraders; Sphingopyxis and Rhodobacter, were also identified. The impact of a number of geochemical conditions, including pH, temperature and SCN- concentration, upon the growth and SCN- degrading capacity of these consortia was determined. These results informed the optimization of a lab-scale thiocyanate degrading bioreactor. In summary, the cultured bacterial consortia proved effective towards SCN- degradation at the prevailing geochemical conditions of the TSF, requiring minimal nutrient additions. These consortia were dominated by genera of known autotrophic SCN- degraders. The comprehensive characterisation of these SCN- degrading consortia will provide the fundamental operational parameters required for deployment of this technique at the field scale.

  1. Electroanalysis of thiocyanate using a novel glassy carbon electrode modified by aryl radicals and cobalt tetracarboxyphthalocyanine

    Energy Technology Data Exchange (ETDEWEB)

    Matemadombo, Fungisai; Nyokong, Tebello [Rhodes University, Grahamstown (South Africa). Department of Chemistry; Westbroek, Philippe [Ghent University, Ghent (Belgium). Department of Textiles

    2007-12-01

    Electrochemical grafting of 4-nitrobenzenediazonium tetrafluoroborate onto a glassy carbon electrode (GCE) results in the formation of a nitrophenyl radical, which reacts with the surface to form a covalent bond (grafting) and results in a nitrophenyl modified electrode. The nitro group is electrochemically reduced to a NH{sub 2} group. Cobalt tetracarboxyphthalocyanine (CoTCPc) complex is then attached to the NH{sub 2} group using 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) and N-hydroxysuccinimide (NHS) as coupling agents. The new CoTCPc modified electrode was characterized using cyclic voltammetry and then employed for the catalytic oxidation of thiocyanate. (author)

  2. Thermal and Mechanical Properties of a Complex Nonlinear Optical Material: Cadmium Mercury Thiocyanate Crystal

    Institute of Scientific and Technical Information of China (English)

    YUAN Duo-Rong; XU Dong; ZHANG Guang-Hui; LIU Ming-Guo; GUO Shi-Yi; MENG Fan-Qing; LU Meng-Kai; FANG Qi; JIANG Min-Hua

    2000-01-01

    Institute of Crystal Materials and State Key Laboratory of Crystal Materials, Shandong University, Ji'nan 250100 (Received 18 March 2000) The data of the thermal expansion and specific heat of cadmium mercury thiocyanate crystal have been obtained. The specific heat is 0.7588J/g℃ at room temperature. The thermal expansion occurs in the direction parallel to the c-axis, and the thermal contraction occurs in the direction parallel to the a-axis. The thermal expansion is the same as the thermal contraction at 353 K. The relationship between thermal properties and crystal structure is discussed.

  3. Determination of Trace Thiocyanate by a Chitosan-Modified Glassy Carbon Electrode

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A chitosan-modified glassy carbon electrode(CMGCE) was employed for the determination of thiocyanate. The measurement was carried out by means of anodic stripping voltammetry. The effects of several experimental parameters, such as pH, the amount of modifier, deposition potential and deposition time were studied for analytical application, respectively. A liner response was obtained in the concentration range of 3.5×10-8-9.3×10-7 g/mL of SCN-. The detection limit was found to be 1.9×10-8 g/mL. The method was satisfactorily used to detect SCN- in saliva.

  4. Gravimetric determination of tungsten with tetraphenylarsonium chloride after its extraction as thiocyanate

    International Nuclear Information System (INIS)

    Small amounts of tungsten in natural and industrial samples can be freed from all important interfering elements by extraction of molybdenum by xanthane, reduction of tungsten by mercury and extraction of tungsten (V) thiocyanate into tribenzylamine, and finally back-extraction. The tungsten can be then determined as tetraphenylarsonium tungstate by precipitating it at pH 2 to 4, filtering it off and drying it at 1100 for 45 min. An overall error of 0.1 to 0.2% is obtained for 5 to 60 mg of tungsten. (author)

  5. Bis(4-chloro-2-cyclohexylimino methyl-phenolate)-two Thiocyanation Cadmium

    Institute of Scientific and Technical Information of China (English)

    ZHANG Xin-Li; LI Zong-Xiao

    2006-01-01

    The title compound (C28H32CdCl2N4O2S2, Mr = 704.00) has been synthesized and characterized by elemental analysis and single-crystal X-ray diffraction. The Schiff base compound is a derivative of 5-chlorosalicylaldehyde. As expected, the molecular structure adopts a trans configuration about the central C=N double bond. It crystallizes in the monoclinic system, space group P21/n with a = 6.003(5), b = 16.490(15), c = 15.698 (14) (A),β = 94.523(12)°, V= 1549(2) (A)3,Z = 2, Dc = 1.509 g/cm3, F(000) = 716 andμ = 1.044 mm-1. A total of 7724 reflections were collected in the range of 2.47~25.01° by using an phi and omega scantechnique, of which 2695 were unique (Rint = 0.0341) and 2258 observed reflections with I > 2δ(Ⅰ) were used in the structure solution and refinement. The complex assumes a distorted octahedral coordination geometry formed by four thiocyanate anions and two Schiff base ligands. The thiocyanate anion bridges the neighboring Cd(Ⅱ) atoms to form the polymeric chains.

  6. Employing Lead Thiocyanate Additive to Reduce the Hysteresis and Boost the Fill Factor of Planar Perovskite Solar Cells

    Energy Technology Data Exchange (ETDEWEB)

    Ke, Weijun [Department of Physics and Astronomy and Wright Center for Photovoltaics Innovation and Commercialization, The University of Toledo, Toledo OH 43606 USA; Key Laboratory of Artificial Micro- and Nano-structures of Ministry of Education of China, School of Physics and Technology, Wuhan University, Wuhan 430072 China; National Renewable Energy Laboratory, 15013 Denver West Parkway Golden CO 80401 USA; Xiao, Chuanxiao [National Renewable Energy Laboratory, 15013 Denver West Parkway Golden CO 80401 USA; Wang, Changlei [Department of Physics and Astronomy and Wright Center for Photovoltaics Innovation and Commercialization, The University of Toledo, Toledo OH 43606 USA; Saparov, Bayrammurad [Department of Mechanical Engineering and Materials Science, Duke University, Durham NC 27708 USA; Department of Chemistry, Duke University, Durham NC 27708 USA; Duan, Hsin-Sheng [Department of Mechanical Engineering and Materials Science, Duke University, Durham NC 27708 USA; Zhao, Dewei [Department of Physics and Astronomy and Wright Center for Photovoltaics Innovation and Commercialization, The University of Toledo, Toledo OH 43606 USA; National Renewable Energy Laboratory, 15013 Denver West Parkway Golden CO 80401 USA; Xiao, Zewen [Department of Physics and Astronomy and Wright Center for Photovoltaics Innovation and Commercialization, The University of Toledo, Toledo OH 43606 USA; Schulz, Philip [National Renewable Energy Laboratory, 15013 Denver West Parkway Golden CO 80401 USA; Harvey, Steven P. [National Renewable Energy Laboratory, 15013 Denver West Parkway Golden CO 80401 USA; Liao, Weiqiang [Department of Physics and Astronomy and Wright Center for Photovoltaics Innovation and Commercialization, The University of Toledo, Toledo OH 43606 USA; Meng, Weiwei [Department of Physics and Astronomy and Wright Center for Photovoltaics Innovation and Commercialization, The University of Toledo, Toledo OH 43606 USA; Yu, Yue [Department of Physics and Astronomy and Wright Center for Photovoltaics Innovation and Commercialization, The University of Toledo, Toledo OH 43606 USA; Cimaroli, Alexander J. [Department of Physics and Astronomy and Wright Center for Photovoltaics Innovation and Commercialization, The University of Toledo, Toledo OH 43606 USA; Jiang, Chun-Sheng [National Renewable Energy Laboratory, 15013 Denver West Parkway Golden CO 80401 USA; Zhu, Kai [National Renewable Energy Laboratory, 15013 Denver West Parkway Golden CO 80401 USA; Al-Jassim, Mowafak [National Renewable Energy Laboratory, 15013 Denver West Parkway Golden CO 80401 USA; Fang, Guojia [Key Laboratory of Artificial Micro- and Nano-structures of Ministry of Education of China, School of Physics and Technology, Wuhan University, Wuhan 430072 China; Mitzi, David B. [Department of Mechanical Engineering and Materials Science, Duke University, Durham NC 27708 USA; Department of Chemistry, Duke University, Durham NC 27708 USA; Yan, Yanfa [Department of Physics and Astronomy and Wright Center for Photovoltaics Innovation and Commercialization, The University of Toledo, Toledo OH 43606 USA

    2016-05-04

    Lead thiocyanate in the perovskite precursor can increase the grain size of a perovskite thin film and reduce the conductivity of the grain boundaries, leading to perovskite solar cells with reduced hysteresis and enhanced fill factor. A planar perovskite solar cell with grain boundary and interface passivation achieves a steady-state efficiency of 18.42%.

  7. Employing Lead Thiocyanate Additive to Reduce the Hysteresis and Boost the Fill Factor of Planar Perovskite Solar Cells.

    Science.gov (United States)

    Ke, Weijun; Xiao, Chuanxiao; Wang, Changlei; Saparov, Bayrammurad; Duan, Hsin-Sheng; Zhao, Dewei; Xiao, Zewen; Schulz, Philip; Harvey, Steven P; Liao, Weiqiang; Meng, Weiwei; Yu, Yue; Cimaroli, Alexander J; Jiang, Chun-Sheng; Zhu, Kai; Al-Jassim, Mowafak; Fang, Guojia; Mitzi, David B; Yan, Yanfa

    2016-07-01

    Lead thiocyanate in the perovskite precursor can increase the grain size of a perovskite thin film and reduce the conductivity of the grain boundaries, leading to perovskite solar cells with reduced hysteresis and enhanced fill factor. A planar perovskite solar cell with grain boundary and interface passivation achieves a steady-state efficiency of 18.42%.

  8. Employing Lead Thiocyanate Additive to Reduce the Hysteresis and Boost the Fill Factor of Planar Perovskite Solar Cells.

    Science.gov (United States)

    Ke, Weijun; Xiao, Chuanxiao; Wang, Changlei; Saparov, Bayrammurad; Duan, Hsin-Sheng; Zhao, Dewei; Xiao, Zewen; Schulz, Philip; Harvey, Steven P; Liao, Weiqiang; Meng, Weiwei; Yu, Yue; Cimaroli, Alexander J; Jiang, Chun-Sheng; Zhu, Kai; Al-Jassim, Mowafak; Fang, Guojia; Mitzi, David B; Yan, Yanfa

    2016-07-01

    Lead thiocyanate in the perovskite precursor can increase the grain size of a perovskite thin film and reduce the conductivity of the grain boundaries, leading to perovskite solar cells with reduced hysteresis and enhanced fill factor. A planar perovskite solar cell with grain boundary and interface passivation achieves a steady-state efficiency of 18.42%. PMID:27145346

  9. Quaternary Ammonium Polyethyleneimine: Antibacterial Activity

    Directory of Open Access Journals (Sweden)

    Ira Yudovin-Farber

    2010-01-01

    Full Text Available 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 g/mL, and Gram-negative, that is, Escherichia coli at 320 g/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 polycations bearing quaternary ammonium moieties inhibit bacterial growth in vitro and have a potential use as additives in medical devices which need antibacterial properties.

  10. Synthesis of Chitosan Quaternary Ammonium Salts

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    A series of N-alkyl or N-aryl chitosan quaternary ammonium salts were prepared via Schiffs base intermediates. Quaternization of N-substituted chitosan derivatives was carried out using methyl iodide to produce water-soluble cationic chitosan quaternary ammonium salt. The products were characterized by IR, 1HNMR and elemental analysis. The degree of substitution of chitosan quaternary ammonium salt was calculated by elemental analysis.

  11. Dicyclohexylammonium thiocyanate

    Directory of Open Access Journals (Sweden)

    Amin Badshah

    2008-02-01

    Full Text Available In the crystal structure of the title compound, C12H24N+·NCS−, the anions and cations are linked through N—H...N and N—H...S hydrogen bonds, resulting in a chain along the a axis.

  12. 33 CFR 126.28 - Ammonium nitrate, ammonium nitrate fertilizers, fertilizer mixtures, or nitro carbo nitrate...

    Science.gov (United States)

    2010-07-01

    ... nitrate fertilizers, fertilizer mixtures, or nitro carbo nitrate; general provisions. 126.28 Section 126..., ammonium nitrate fertilizers, fertilizer mixtures, or nitro carbo nitrate; general provisions. (a) When any item of ammonium nitrate, ammonium nitrate fertilizers, fertilizer mixtures, or nitro carbo...

  13. 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 s

  14. Nucleation studies and characterization of potassium thiocyanate added KDP crystals grown by seed rotation technique

    Energy Technology Data Exchange (ETDEWEB)

    Dhanaraj, P.V. [Centre for Crystal Growth, SSN College of Engineering, Kalavakkam 603 110 (India); Rajesh, N.P., E-mail: rajeshnp@ssn.edu.i [Centre for Crystal Growth, SSN College of Engineering, Kalavakkam 603 110 (India); Mahadevan, C.K. [Physics Research Centre, S.T. Hindu College, Nagercoil 629 002 (India); Bhagavannarayana, G. [C.G.C. Section, National Physical Laboratory, New Delhi 110 012 (India)

    2009-08-01

    The effect of the addition of potassium thiocyanate on potassium dihydrogen phosphate (KDP) crystals, grown from aqueous solution by the temperature lowering method using a microcontroller based seed rotation technique has been studied. As part of nucleation studies, metastable zone width, induction period and crystal growth rate of additive added KDP are determined and analyzed with the pure system. Dielectric measurements were carried out on pure and doped crystals at various temperatures ranging from 313 to 423 K and compared. The crystalline perfection of the grown crystal was studied by the high resolution X-ray diffraction analysis. The crystal grown from additive added solution was subjected to structural, optical transmission, second harmonic generation and hardness studies and the effect of additive on pure system is investigated.

  15. Spectrophotometric determination of uranium in sea water with thiocyanate and rhodamine B

    International Nuclear Information System (INIS)

    In the presence of a large excess of thiocyanate uranium(VI) forms a violet colour with Rhodamine B. The complex can be stabilized by addition of poly(vinyl alcohol). The calibration graph for measurement at 600 nm is linear in the range 0.5-10 μg of uranium per 25 ml, the molar absorptivity being 3.56 x 105l x mole-1 x cm-1. The effect of foreign ions has been studied and the method can be applied to the determination of uranium in sea-water, with reliable results. Uranium is preconcentrated from sea-water by a flotation procedure with toluene in presence of benzoate and Safranine T, with nitrilotriacetic acid as masking agent. The method is highly selective for uranium, with a recovery of 97.9-99.2%. (Author)

  16. Copper thiocyanate: An attractive hole transport/extraction layer for use in organic photovoltaic cells

    International Nuclear Information System (INIS)

    We report the advantageous properties of the inorganic molecular semiconductor copper(I) thiocyanate (CuSCN) for use as a hole collection/transport layer (HTL) in organic photovoltaic (OPV) cells. CuSCN possesses desirable HTL energy levels [i.e., valence band at −5.35 eV, 0.35 eV deeper than poly(3,4-ethylenedioxythiophene):polystyrenesulfonate (PEDOT:PSS)], which produces a 17% increase in power conversion efficiency (PCE) relative to PEDOT:PSS-based devices. In addition, a two-fold increase in shunt resistance for the solar cells measured in dark conditions is achieved. Ultimately, CuSCN enables polymer:fullerene based OPV cells to achieve PCE > 8%. CuSCN continues to offer promise as a chemically stable and straightforward replacement for the commonly used PEDOT:PSS

  17. Radiochemical extraction of lanthanide thiocyanate complexes with bis-2-ethylhexyl sulphoxide

    International Nuclear Information System (INIS)

    The extraction of lanthanides (Ln) such as Nd(III), Eu(III) and Er(III) from thiocyanate solutions by bis-2-ethylhexyl sulphoxide (B2EHSO) in benzene has been studied by tracer techniques. For comparison, extraction studies have been carried out with di-n-octyl sulphoxide (DOSO) and tri-octyl phosphine oxide (TOPO). Extraction studies have also been carried out with mixtures of B2EHSO and DOSO or TOPO. A relatively small synergistic enhancement has been observed with a mixture of extractants, which may be due to the formation of more stable mixed-ligand complexes. The extraction data have been analysed by both graphical and theoretical methods taking into account aqueous phase speciation and all plausible complexes extracted into the organic phase. The equilibrium constants of the extracted species were determined by non-linear regression analysis. (orig.)

  18. Amperometric Sensor Used for Determination of Thiocyanate with a Silver Nanoparticles Modified Electrode

    Directory of Open Access Journals (Sweden)

    Bin Fang

    2004-10-01

    Full Text Available Abstract: A novel electrode modified with silver nanoparticles was fabricated. It is found that the reducibility of silver nanoparticles is higher than for bulk silver by comparing a silver nanoparticles modified electrode with a silver micro-disk electrode. When SCN- was added, a new oxidation peak occurred and the anodic peak current of silver nanoparticles decreased. The new anodic peak current is proportional to the thiocyanate concentration in the range of 5.0×10-7~4.0×10-4 mol/L in pH 6.0 NaH2PO4-Na2HPO4 buffer solutions (PBS. The detection limit (S/N=3 is 4×10-8 mol/L. This method has been applied to the determination of saliva (smoker and non-smoker.

  19. Inhibition of carbon steel corrosion in 1 M HCl medium by potassium thiocyanate

    Directory of Open Access Journals (Sweden)

    A. Anejjar

    2014-04-01

    Full Text Available The effect of potassium thiocyanate (KSCN on the corrosion of carbon steel (C-steel in 1 M HCl has been investigated in relation to the concentration of the inhibitor by polarization curves, electrochemical impedance spectroscopy and weight loss measurement. The results obtained revealed that this compound is a good mixed type inhibitor with predominant cathodic effectiveness. The effect of temperature on the corrosion behavior with the addition of optimal concentration of KSCN was studied in the temperature range 298–328 K. The value of inhibition efficiency decreases slightly with the increase in temperature. Changes in impedance parameters (charge transfer resistance, Rct, and double layer capacitance, Cdl were indicative of adsorption of KSCN on the metal surface, leading to the formation of a protective film. Adsorption of KSCN on the C-steel surface was found to obey the Langmuir adsorption isotherm. Some thermodynamic functions of dissolution and adsorption processes were also determined and discussed.

  20. Copper thiocyanate: An attractive hole transport/extraction layer for use in organic photovoltaic cells

    Energy Technology Data Exchange (ETDEWEB)

    Treat, Neil D., E-mail: neil.treat@imperial.ac.uk, E-mail: t.anthopoulos@imperial.ac.uk; Stingelin, Natalie [Department of Materials and Centre for Plastic Electronics, Imperial College London, South Kensington Campus, London SW7 2AZ (United Kingdom); Yaacobi-Gross, Nir; Faber, Hendrik; Perumal, Ajay K.; Bradley, Donal D. C.; Anthopoulos, Thomas D., E-mail: neil.treat@imperial.ac.uk, E-mail: t.anthopoulos@imperial.ac.uk [Department of Physics and Centre for Plastic Electronics, Blackett Laboratory, Imperial College London, South Kensington Campus, London SW7 2AZ (United Kingdom)

    2015-07-06

    We report the advantageous properties of the inorganic molecular semiconductor copper(I) thiocyanate (CuSCN) for use as a hole collection/transport layer (HTL) in organic photovoltaic (OPV) cells. CuSCN possesses desirable HTL energy levels [i.e., valence band at −5.35 eV, 0.35 eV deeper than poly(3,4-ethylenedioxythiophene):polystyrenesulfonate (PEDOT:PSS)], which produces a 17% increase in power conversion efficiency (PCE) relative to PEDOT:PSS-based devices. In addition, a two-fold increase in shunt resistance for the solar cells measured in dark conditions is achieved. Ultimately, CuSCN enables polymer:fullerene based OPV cells to achieve PCE > 8%. CuSCN continues to offer promise as a chemically stable and straightforward replacement for the commonly used PEDOT:PSS.

  1. Life-threatening intoxication with methylene bis(thiocyanate: clinical picture and pitfalls. A case report

    Directory of Open Access Journals (Sweden)

    Schnuelle Peter

    2006-04-01

    Full Text Available Abstract Background Methylene bis(thiocyanate (MBT is a microbiocidal agent mainly used in industrial water cooling systems and paper mills as an inhibitor of algae, fungi, and bacteria. Case presentation We describe the first case of severe intoxication following inhalation of powder in an industrial worker. Profound cyanosis and respiratory failure caused by severe methemoglobinemia developed within several minutes. Despite immediate admission to the intensive care unit, where mechanical ventilation and hemodialysis for toxin elimination were initiated, multi-organ failure involving liver, kidneys, and lungs developed. While liver failure was leading, the patient was successfully treated with the MARS (molecular adsorbent recirculating system procedure. Conclusion Intoxication with MBT is a potentially life-threatening intoxication causing severe methemoglobinemia and multi-organ failure. Extracorporeal liver albumin dialysis (MARS appears to be an effective treatment to allow recovery of hepatic function.

  2. Seed-mediated growth of palladium nanocrystals: The effect of pseudo-halide thiocyanate ions

    Science.gov (United States)

    Zhang, Ling; Niu, Wenxin; Xu, Guobao

    2011-02-01

    In synthesis in a solution phase, adsorbates such as halides can interact selectively with different metal crystal facets and affect the final morphology of nanocrystals. Pseudo-halide thiocyanate ions (SCN-) can also adsorb on the metal surface, but they have never been used for the synthesis of shape-controlled colloidal metal nanocrystals. In this study, we first investigated the effect of SCN- on the morphology of palladium nanocrystals through a seed-mediated growth method. The presence of 1 µM SCN- in the growth solutions could lead to the formation of palladium polyhedra: truncated rhombic dodecahedra enclosed by twelve {110}, eight {111} and six {100} facets. The products were nanocubes enclosed with six {100} facets if cetyltrimethylammonium bromide (CTAB) was the only capping agent. Meanwhile, the mechanism of the effect of SCN- on the morphology of Pd nanocrystals is discussed.In synthesis in a solution phase, adsorbates such as halides can interact selectively with different metal crystal facets and affect the final morphology of nanocrystals. Pseudo-halide thiocyanate ions (SCN-) can also adsorb on the metal surface, but they have never been used for the synthesis of shape-controlled colloidal metal nanocrystals. In this study, we first investigated the effect of SCN- on the morphology of palladium nanocrystals through a seed-mediated growth method. The presence of 1 µM SCN- in the growth solutions could lead to the formation of palladium polyhedra: truncated rhombic dodecahedra enclosed by twelve {110}, eight {111} and six {100} facets. The products were nanocubes enclosed with six {100} facets if cetyltrimethylammonium bromide (CTAB) was the only capping agent. Meanwhile, the mechanism of the effect of SCN- on the morphology of Pd nanocrystals is discussed. Electronic supplementary information (ESI) available: Additional SEM, TEM and XRD data. See DOI: 10.1039/c0nr00622j

  3. Two arginine residues in the substrate pocket predominantly control the substrate selectivity of thiocyanate hydrolase.

    Science.gov (United States)

    Yamanaka, Yasuaki; Arakawa, Takatoshi; Watanabe, Toshinori; Namima, Satoshi; Sato, Masa; Hori, Shota; Ohtaki, Akashi; Noguchi, Keiichi; Katayama, Yoko; Yohda, Masafumi; Odaka, Masafumi

    2013-07-01

    Thiocyanate hydrolase (SCNase) of Thiobacillus thioparus THI115 is a cobalt (Co)-containing enzyme that catalyzes the hydrolysis of thiocyanate (SCN⁻), a major component of wastewater from coke oven factories, to carbonyl sulfide and ammonia. Although SCNase exhibits high structural similarities to Co-type nitrile hydratase (NHase), including a unique Co³⁺ catalytic center with two oxidized Cys ligands, both SCNase and NHase exclusively catalyze only their own substrates. Based on the differences in the substrate-binding pockets of these enzymes, βArg90 and γArg136 of SCNase, with side chains extending toward the pocket, were separately substituted with Phe and Trp, the corresponding residues, respectively, in Co-type NHase. Both SCNase βArg90 and SCNase γArg136 mutants showed no SCN⁻ hydrolysis activity but did catalyze the hydration of nitriles. The estimated kcat values (∼2 s⁻¹) corresponded to approximately 0.2% of that of Co-type NHase for nitrile hydration and approximately 3% of that of wild-type SCNase for SCN⁻ hydrolysis. The crystal structure of SCNase γR136W is essentially identical to that of the wild-type, including the Co³⁺ center having Cys oxidations; the size of the substrate pocket was enlarged because of conformational changes on the side chains of the mutated residue. Discussion of the difference in the environments around the substrate-binding pockets among the wild-type and mutant SCNases and Co-type NHase strongly suggests that βArg90 and γArg136, positioned at the top of the Co³⁺ center, predominantly control the substrate selectivity of SCNase. PMID:23453853

  4. Thiocyanate binding to the molybdenum centre of the periplasmic nitrate reductase from Paracoccus pantotrophus.

    Science.gov (United States)

    Butler, C S; Charnock, J M; Garner, C D; Thomson, A J; Ferguson, S J; Berks, B C; Richardson, D J

    2000-12-15

    The periplasmic nitrate reductase (NAP) from Paracoccus pantotrophus is a soluble two-subunit enzyme (NapAB) that binds two haem groups, a [4Fe-4S] cluster and a bis(molybdopterin guanine dinucleotide) (MGD) cofactor that catalyses the reduction of nitrate to nitrite. In the present study the effect of KSCN (potassium thiocyanate) as an inhibitor and Mo ligand has been investigated. Results are presented that show NAP is sensitive to SCN(-) (thiocyanate) inhibition, with SCN(-) acting as a competitive inhibitor of nitrate (K(i) approximately 4.0 mM). The formation of a novel EPR Mo(V) species with an elevated g(av) value (g(av) approximately 1.994) compared to the Mo(V) High-g (resting) species was observed upon redox cycling in the presence of SCN(-). Mo K-edge EXAFS analysis of the dithionite-reduced NAP was best fitted as a mono-oxo Mo(IV) species with three Mo-S ligands at 2.35 A (1 A=0.1 nm) and a Mo-O ligand at 2.14 A. The addition of SCN(-) to the reduced Mo(IV) NAP generated a sample that was best fitted as a mono-oxo (1.70 A) Mo(IV) species with four Mo-S ligands at 2.34 A. Taken together, the competitive nature of SCN(-) inhibition of periplasmic nitrate reductase activity, the elevated Mo(V) EPR g(av) value following redox cycling in the presence of SCN(-) and the increase in sulphur co-ordination of Mo(IV) upon SCN(-) binding, provide strong evidence for the direct binding of SCN(-) via a sulphur atom to Mo. PMID:11104696

  5. Efficient separation of transition metals from rare earths by an undiluted phosphonium thiocyanate ionic liquid.

    Science.gov (United States)

    Rout, Alok; Binnemans, Koen

    2016-06-21

    The ionic liquid trihexyl(tetradecyl)phosphonium thiocyanate has been used for the extraction of the transition metal ions Co(ii), Ni(ii), Zn(ii), and the rare-earth ions La(iii), Sm(iii) and Eu(iii) from aqueous solutions containing nitrate or chloride salts. The transition metal ions showed a high affinity for the ionic liquid phase and were efficiently extracted, while the extraction efficiency of the rare-earth ions was low. This difference in extraction behavior enabled separation of the pairs Co(ii)/Sm(iii), Ni(ii)/La(iii) and Zn(ii)/Eu(iii). These separations are relevant for the recycling of rare earths and transition metals from samarium cobalt permanent magnets, nickel metal hydride batteries and lamp phosphors, respectively. The extraction of metal ions from a chloride or nitrate solution with a thiocyanate ionic liquid is an example of "split-anion extraction", where different anions are present in the aqueous and ionic liquid phase. Close to 100% loading was possible for Co(ii) and Zn(ii) up to a concentration of 40 g L(-1) of the transition metal salt in the initial aqueous feed solution, whereas the extraction efficiency for Ni(ii) gradually decreased with increase in the initial feed concentration. Stripping of Co(ii), Zn(ii) and Ni(ii) from the loaded ionic liquid phase was possible by a 15 wt% NH3 solution. The ionic liquid could reused after extraction and stripping. PMID:27243450

  6. Vibrational dynamics of thiocyanate and selenocyanate bound to horse heart myoglobin

    Energy Technology Data Exchange (ETDEWEB)

    Maj, Michał; Oh, Younjun; Park, Kwanghee; Lee, Jooyong; Cho, Minhaeng, E-mail: mcho@korea.ac.kr [Department of Chemistry, Korea University, Seoul 136-713 (Korea, Republic of); Kwak, Kyung-Won [Department of Chemistry, Chung-Ang University, Seoul 156-756, SouthKorea (Korea, Republic of)

    2014-06-21

    The structure and vibrational dynamics of SCN- and SeCN-bound myoglobin have been investigated using polarization-controlled IR pump-probe measurements and quantum chemistry calculations. The complexes are found to be in low and high spin states, with the dominant contribution from the latter. In addition, the Mb:SCN high spin complex exhibits a doublet feature in the thiocyanate stretch IR absorption spectra, indicating two distinct molecular conformations around the heme pocket. The binding mode of the high spin complexes was assigned to occur through the nitrogen atom, contrary to the binding through the sulfur atom that was observed in myoglobin derived from Aplysia Limacina. The vibrational energy relaxation process has been found to occur substantially faster than those of free SCN{sup −} and SeCN{sup −} ions and neutral SCN- and SeCN-derivatized molecules reported previously. This supports the N-bound configurations of MbNCS and MbNCSe, because S- and Se-bound configurations are expected to have significantly long lifetimes due to the insulation effect by heavy bridge atom like S and Se in such IR probes. Nonetheless, even though their lifetimes are much shorter than those of corresponding free ions in water, the vibrational lifetimes determined for MbNCS and MbNCSe are still fairly long compared to those of azide and cyanide myoglobin systems studied before. Thus, thiocyanate and selenocyanate can be good local probes of local electrostatic environment in the heme pocket. The globin dependence on binding mode and vibrational dynamics is also discussed.

  7. Vibrational dynamics of thiocyanate and selenocyanate bound to horse heart myoglobin

    Science.gov (United States)

    Maj, Michał; Oh, Younjun; Park, Kwanghee; Lee, Jooyong; Kwak, Kyung-Won; Cho, Minhaeng

    2014-06-01

    The structure and vibrational dynamics of SCN- and SeCN-bound myoglobin have been investigated using polarization-controlled IR pump-probe measurements and quantum chemistry calculations. The complexes are found to be in low and high spin states, with the dominant contribution from the latter. In addition, the Mb:SCN high spin complex exhibits a doublet feature in the thiocyanate stretch IR absorption spectra, indicating two distinct molecular conformations around the heme pocket. The binding mode of the high spin complexes was assigned to occur through the nitrogen atom, contrary to the binding through the sulfur atom that was observed in myoglobin derived from Aplysia Limacina. The vibrational energy relaxation process has been found to occur substantially faster than those of free SCN- and SeCN- ions and neutral SCN- and SeCN-derivatized molecules reported previously. This supports the N-bound configurations of MbNCS and MbNCSe, because S- and Se-bound configurations are expected to have significantly long lifetimes due to the insulation effect by heavy bridge atom like S and Se in such IR probes. Nonetheless, even though their lifetimes are much shorter than those of corresponding free ions in water, the vibrational lifetimes determined for MbNCS and MbNCSe are still fairly long compared to those of azide and cyanide myoglobin systems studied before. Thus, thiocyanate and selenocyanate can be good local probes of local electrostatic environment in the heme pocket. The globin dependence on binding mode and vibrational dynamics is also discussed.

  8. Purification of bovine milk lactoperoxidase and investigation of antibacterial properties at different thiocyanate mediated.

    Science.gov (United States)

    Uğuz, M T; Ozdemir, H

    2005-01-01

    Bovine lactoperoxidase (LPO) was purified with amberlite CG 50 H+ resin, CM sephadex C-50 ion-exchange chromatography, and sephadex G-100 gel filtration chromatography from skim milk. The activity of lactoperoxidase was measured by using 2.2-azino-bis (3-ethylbenzthiazoline-6 sulfonic acid) diammonium salt (ABTS) as a choromogenic substrate at pH 6.0. Purification degree for the purified enzyme was controlled with SDS-PAGE and Rz value (A412/A280). Rz value for the purified LPO was 0.8. Km value at pH 6.0 at 20 degrees C for the LPO was 0.20 mM. Vmax value was 7.87 micromol/ml min at pH 6.0 at 20 degrees C. Bovine LPO showed high antibacterial activity in 100 mM thiocyanate--100 mM H2O2 medium for some pathogenic bacteria, such as Aeromonas hydrophila ATCC 7966, Micrococcus luteus LA 2971, Mycobacterium smegmatis RUT, Bacillus subtilis IMG 22, Pseudomonas pyocyanea, Bacillus subtilis var. niger ATCC 10, Pseudomonas aeruginosa ATCC 27853, Enterococcus faecalis ATCC 15753, Bacillus brevis FMC3, Klebsiella pneumoniae FMC 5, Corynebacterium xerosis UC 9165, Bacillus cereus EU, Bacillus megaterium NRS, Yersinia enterocolytica, Listeria monocytogenes scoot A, Bacillus megaterium EU, Bacillus megaterium DSM32, Klebsiella oxytocica, Staphylococcus aerogenes, Streptococcus faecalis, Mycobacterium smegmatis CCM 2067 and compared with well known antibacterial substances such as penicilline, ampicilline, amoxicillin-clavulanate and ceftriaxon. The LPO--100 mM thiocyanate--100 mM H2O2 system was purposed as an effective agent against many of the diseases causing organisms in human and animals.

  9. Atmospheric behaviour of ammonia and ammonium.

    NARCIS (Netherlands)

    Asman, W.A.J.

    1987-01-01

    1.4.1 Scope of this thesisA 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 into account, nor we

  10. [3,3]-sigmatropic rearrangements of fluorinated allyl (Thio)cyanates - a tool for the synthesis of fluorinated (Thio)ureas.

    Science.gov (United States)

    Ramb, Daniel C; Kost, Lisa; Haufe, Günter

    2014-01-01

    The first (thio)cyanate to iso(thio)cyanate rearrangements based on 2-fluoroallylic alcohols are presented. Long-chain 2-fluoroallylic alcohols were converted to corresponding N-unsubstituted carbamates by treatment with trichloroacetyl isocyanate. Dehydration using trifluoroacetic anhydride in the presence of triethylamine formed intermediate allylic cyanates, which immediately underwent sigmatropic rearrangement to fluorinated allyl isocyanates. Without isolation the latter delivered fluorinated ureas by addition of amines. The thiocyanate to isothiocyanate rearrangements started from the same fluorinated allylic alcohols, which were first converted to mesylates. Heating in THF with potassium thiocyanate led to fluorinated allyl isothiocyanates, via [3,3]-sigmatropic rearrangement of intermediate allyl thiocyanates. The formed products were further reacted with amines to fluorinated thioureas.

  11. 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...

  12. Research on Processes of Erythromycin Thiocyanate Crystallization and Production of Erythromycin with Crude Erythromycin Thiocyanate%水相结晶硫氰酸红霉素及其转红霉素碱工艺研究

    Institute of Scientific and Technical Information of China (English)

    姬红明; 王勇平; 张永乐; 高继东

    2014-01-01

    通过对红霉素的水相浓缩液进行硫氰酸红霉素结晶工艺的探讨,并对此方法所得的硫氰酸红霉素粗品转红霉素碱的工艺进行研究,以期缩短红霉素的生产过程,减少生产过程中的物料损失,有效提高红霉素的总收率。%Through the discussion of erythromycin thiocyanate crystallization process in which water-phase erythromycin condensed solution is used, the process of crude erythromycin thiocyanate being transformed into erythromycin was studied. It is hoped that with the results in the study in this paper erythromycin production period and the loss of materials used in production can be reduced, and total yield rate for erythromycin can be enhanced.

  13. Ammonium and attachment of Rhodopirellula baltica.

    Science.gov (United States)

    Frank, Carsten S; Langhammer, Philipp; Fuchs, Bernhard Maximilian; Harder, Jens

    2011-05-01

    A dimorphic life cycle has been described for the planctomycete Rhodopirellula baltica SH1(T), with juvenile motile, free-swimming cells and adult sessile, attached-living cells. However, attachment as a response to environmental factors was not investigated. We studied the response of R. baltica to nitrogen limitation. In batch cultures, ammonium limitation coincided with a dominance of free-swimming cells and a low number of aggregates. Flow cytometry revealed a quantitative shift with increasing ammonium availability, from single cells towards attached cells in large aggregates. During growth of R. baltica on glucose and ammonium in chemostats, an ammonium addition caused a macroscopic change of the growth behaviour, from homogeneous growth in the liquid phase to a biofilm on the borosilicate glass wall of the chemostat vessel. Thus, an ammonium limitation-a carbon to nitrogen supply ratio of 30:1-sustained free-living growth without aggregate formation. A sudden increase in ammonium supply induced sessile growth of R. baltica. These observations reveal a response of Rhodopirellula baltica cells to ammonium: they abandon the free-swimming life, attach to particles and form biofilms. PMID:21340506

  14. Study of crystalline perfection and thermal analysis of zinc cadmium thiocyanate single crystals grown in silica gel

    Energy Technology Data Exchange (ETDEWEB)

    Nisha Santha Kumari, P. [Department of Physics, Auxilium College, Vellore (India); Kalainathan, S. [School of Science and Humanities, VIT University, Vellore (India); Bhagavannarayana, G. [Materials Characterization Division, National Physical Laboratory, New Delhi (India)

    2008-03-15

    Zinc cadmium thiocyanate ZnCd(SCN){sub 4} abbreviated as ZCTC is a bimetallic thiocyanate complex that exhibits excellent nonlinear optical property. Single crystals of ZCTC have been grown in silica gel by the process of diffusion. Colorless transparent crystals of size 12 mm x 2 mm x 1.3 mm have been obtained. High resolution X-ray diffraction study was carried out to investigate the crystalline perfection of the grown crystal and the quality of the crystal was found to be quite good. Thermal stability of the grown crystal was investigated by thermogravimetric and differential thermal analyses. Fourier Transform Infrared spectrum was recorded to confirm the functional groups. Microhardness of the crystal is also studied. Being a nonlinear optical material, a comparative study of its second harmonic generation efficiency with urea has been made. (copyright 2007 WILEY -VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  15. Ultrafast Structural Fluctuations of Myoglobin-Bound Thiocyanate and Selenocyanate Ions Measured with Two-Dimensional Infrared Photon Echo Spectroscopy.

    Science.gov (United States)

    Maj, Michał; Kwak, Kyungwon; Cho, Minhaeng

    2015-11-16

    Structural dynamics within the distal cavity of myoglobin protein is investigated using 2D-IR and IR pump-probe spectroscopy of the N≡C stretch modes of heme-bound thiocyanate and selenocyanate ions. Although myoglobin-bound thiocyanate group shows a doublet in its IR absorption spectrum, no cross peaks originating from chemical exchange between the two components are observed in the time-resolved 2D IR spectra within the experimental time window. Frequency-frequency correlation functions of the two studied anionic ligands are obtained by means of a few different analysis approaches; these functions were then used to elucidate the differences in structural fluctuation around ligand, ligand-protein interactions, and the degree of structural heterogeneity within the hydrophobic pocket of these myoglobin complexes.

  16. In situ Determination of Fluoride in Groundwater Using N-Octyl Acetamide with Iron(III)-Thiocyanate Complex

    Science.gov (United States)

    Sahin, R.; Tapadia, K.; Sharma, A.

    2016-07-01

    This paper describes the nanodrop spectrophotometric determination of fluoride (F-) in a ground water sample using the organic reagent N-octylacetamide (N-OAA) with iron(III)-thiocyanate complex. The iron(III)-thiocyanate complex was extracted with a chloroform solution of amide (N-phenylacetamide, N-alkylacetamide, alkyl = butyl, phenyl, hexyl, and octyl group). This method is based upon the bleaching effect of fluoride on the red-colored extracted complex of iron(III)-thiocyanate-OAA in chloroform. The absorbance of the extract was measured pre and post F- addition at λmax = 470 nm against the reagent blank. The limit of detection and %RSD of F- was 38 μg/L and ±1.6%. The designed work followed Beer's law between 0.5 to 10 μg/mL with slope, intercept, and correlation coefficient values of -0.1101, 1.116, and -0.997, respectively. Furthermore, the applicability of the present investigation was extended for the determination of F- in a groundwater sample, and the results obtained were compared with those from another reported method.

  17. A comparative study on the aggregating effects of guanidine thiocyanate, guanidine hydrochloride and urea on lysozyme aggregation

    Energy Technology Data Exchange (ETDEWEB)

    Emadi, Saeed, E-mail: emadi@iasbs.ac.ir; Behzadi, Maliheh

    2014-08-08

    Highlights: • Lysozyme aggregated in guanidine thiocyanate (1.0 and 2.0 M). • Lysozyme aggregated in guanidine hydrochloride (4 and 5 M). • Lysozyme did not aggregated at any concentration (0.5–5 M) of urea. • Unfolding pathway is more important than unfolding per se in aggregation. - Abstract: Protein aggregation and its subsequent deposition in different tissues culminate in a diverse range of diseases collectively known as amyloidoses. Aggregation of hen or human lysozyme depends on certain conditions, namely acidic pH or the presence of additives. In the present study, the effects on the aggregation of hen egg-white lysozyme via incubation in concentrated solutions of three different chaotropic agents namely guanidine thiocyanate, guanidine hydrochloride and urea were investigated. Here we used three different methods for the detection of the aggregates, thioflavin T fluorescence, circular dichroism spectroscopy and atomic force microscopy. Our results showed that upon incubation with different concentrations (0.5, 1.0, 2.0, 3.0, 4.0, 5.0 M) of the chemical denaturants, lysozyme was aggregated at low concentrations of guanidine thiocyanate (1.0 and 2.0 M) and at high concentrations of guanidine hydrochloride (4 and 5 M), although no fibril formation was detected. In the case of urea, no aggregation was observed at any concentration.

  18. Use of the molybdenum-thiocyanate-rhodamine 6G ternary complex for spectrophotometric molybdenum determination without extraction

    International Nuclear Information System (INIS)

    A modified thiocyanate method without extraction by using rhodamine 6G as a secondary ligand was developed. Molybdenum in 1.0x10-2 M HCl, after the addition of ascorbic acid, was heated for 10 min in a 90 deg. C water bath for reduction. Suitable amounts of glycerine, Triton X-100, rhodamine 6G solutions and 2+1 (v/v) 9 M H2SO4+3 M KHSO4 were added in this order. This solution was allowed to cool to room temperature and the absorbance at 570 nm was measured against a reagent blank 45 min after the addition of thiocyanate solution and the second aliquot of Triton X-100 solution. The complex was stable for at least 4 h, the order of reagent addition was important, and thiocyanate should be in large excess. Beer's law was obeyed over the range 0.9x10-6 to 1.1x10-5 M Mo with the molar absorptivity being 1.1x105 l mol-1 cm-1. The R.S.D. for the determination of 0.7 mg Mo l-1 was 1.83% (n=8). Possible interferences of various cations and anions on molybdenum determination were studied. The proposed method was applied to the determination of molybdenum in a dental alloy, Wiron 99

  19. Structures of Trichloromethyl Thiocyanate, CCl3 SCN, in Gaseous and Crystalline State.

    Science.gov (United States)

    Berrueta Martínez, Yanina; Rodríguez Pirani, Lucas S; Erben, Mauricio F; Boese, Roland; Reuter, Christian G; Vishnevskiy, Yury V; Mitzel, Norbert W; Della Védova, Carlos O

    2016-05-18

    Trichloromethyl thiocyanate, CCl3 SCN, was structurally studied in both the gas and crystal phases by means of gas electron diffraction (GED) and single-crystal X-ray diffraction (XRD), respectively. Both experimental studies and quantum chemical calculations indicate a staggered orientation of the CCl3 group relative to the SCN group. This conclusion is supported by the similarity of the C-SCN bond length to that of the anti-structure of CH2 ClSCN (Berrueta Martínez et al. Phys. Chem. Chem. Phys. 2015, 17, 15805-15812). Bond lengths and angles are similar for gas and crystal CCl3 SCN structures; however, the crystal structure presents different intermolecular interactions. These include halogen and chalcogen type interactions, the geometry of which was studied. Characteristic C-Y⋅⋅⋅N angles (Y=Cl or S) close to 180° provide evidence for typical σ-hole interactions along the halogen/chalcogen-carbon bond in N⋅⋅⋅Cl and N⋅⋅⋅S, intermolecular units. PMID:26865044

  20. Determination of free acid by standard addition method in potassium thiocyanate

    Energy Technology Data Exchange (ETDEWEB)

    Baumann, E W

    1982-06-01

    The free acid content of solutions containing hydrolyzable ions has been determined potentiometrically by a standard addition method. Two increments of acid are added to the sample in 1M potassium thiocyanate solution. The sample concentration is calculated by solution of three simultaneous Nernst equations. The method has been demonstrated for solutions containing Al/sup 3 +/, Cr/sup 3 +/, Fe/sup 3 +/, Hg/sup 2 +/, Ni/sup 2 +/, Th/sup 4 +/, or UO/sub 2//sup 2 +/ with a metal-to-acid ratio of < 2.5. The method is suitable for determination of 10 ..mu..moles acid in 10 mL total volume. The accuracy can be judged from the agreement of the Nernst slopes found in the presence and absence of hydrolyzable ions. The relative standard deviation is < 2.5%. The report includes a survey of experiments with thermometric, pH, and Gran plot titrations in a variety of complexants, from which the method was evolved. Also included is a literature survey of sixty references, a discussion of the basic measurements, and a complete analytical procedure.

  1. Syntheses of fluorescent thiocyanate supramolecular compounds with unusual two-dimensional structures

    Science.gov (United States)

    Bie, Hai-Ying; Lu, Jing; Yu, Jie-Hui; Xu, Ji-Qing; Zhao, Kui; Zhang, Xiao

    2005-05-01

    Three novel thiocyanate supramolecular compounds have been synthesized and characterized by X-ray diffraction and fluorescent spectra. Compound [pipH] 2[Co(NCS) 4] (pip=piperazine) 1 possesses a two-dimensional layer connected by the combination of N-H⋯N hydrogen bonds and weak S⋯S contacts. Under the same conditions, using nickel salt instead of cobalt salt as a starting material, we obtained a different two-dimensional supramolecular layer [pipH] 2[Ni(NCS) 4] 2 connected by unusual N-H⋯S hydrogen bonds and weak S⋯S contacts. In order to observe the influence of the dimension of ligand on the self-assembly structure, dabco was used for substituting pip, and compound [dabcoH] 2[Ni(NCS) 4] (dabco=1,4-Diazabicyclo[2.2.2] octane) 3 was gained, which constructed two-dimensional, highly wavy network with hourglass-shaped cavities only through N-H⋯S hydrogen bonds.

  2. Electrical properties of biodegradable poly(ε-caprolactone): lithium thiocyanate complexed polymer electrolyte films

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • The minimum Tm and χc values are observed in 15 wt% LiSCN complexed film. • The conductivity of PCL:LiSCN complexed films follows Johnscher's power law. • Conductivity and dielectric constant follows the same trend. • The charge carriers responsible for both conduction and relaxation are the same. - Abstract: Lithium ion conducting polymer electrolyte films based on biodegradable poly(ε-caprolactone) (PCL) complexed with lithium thiocyanate (LiSCN) salt were prepared by solution cast technique. Thermal and electrical properties of the polymer electrolyte films were studied using differential scanning calorimetry (DSC) and ac impedance spectroscopy. In order to investigate the ion conduction mechanism and relaxation behavior of complex polymer electrolyte films, the conductivity, dielectric constant, loss tangent and electric modulus were analyzed as a function of frequency and temperature. The variation of conductivity with frequency obeyed the Johnscher's power law. The dielectric constant exhibited a higher value at a lower frequency and increased with rising temperature due to the polar nature of host polymer. The activation energies for both dc conductivity and relaxation had the same value (∼0.87 eV), implying that the charge carriers responsible for both conduction and relaxation were the same

  3. Paper-based analytical device for instrumental-free detection of thiocyanate in saliva as a biomarker of tobacco smoke exposure.

    Science.gov (United States)

    Pena-Pereira, Francisco; Lavilla, Isela; Bendicho, Carlos

    2016-01-15

    This work describes a fast and simple assay for in situ detection of thiocyanate, i.e., a biomarker of tobacco smoke exposure, in human saliva. The assay is based on the formation of an iron(III)-thiocyanate colored complex in a paper-based sensing platform and subsequent image analysis using a scanner as detection device. Experimental parameters influencing the color intensity of the complex were fully evaluated, including the selection of detection conditions, type of paper substrate, test zone dimensions and composition as well as the stability of the paper-based device. Under optimal conditions, the detection limit was 0.06mM of thiocyanate, and the repeatability, expressed as relative standard deviation, was 3%. The proposed method, characterized by its simplicity, portability and low sample consumption, was applied to the detection of thiocyanate in a series of human saliva samples. Average thiocyanate levels in the ranges 0.28-0.87mM and 0.78-4.28mM were found for non-smokers and smokers, respectively. Recovery studies were carried out at two concentration levels, showing recovery values in the range of 96.1-103.6%.

  4. Natural Nitrogen—15 Abundance of Ammonium Nitrogen and Fixed Ammonium in Soils

    Institute of Scientific and Technical Information of China (English)

    SHISHU-LIAN; XINGGUANG-XI; 等

    1992-01-01

    The present article deals with the natural nitrogen-15 abundance of ammonium nitrogen and fixed ammonium in different soils.Variations in the natural 15N abundance of ammonium nitrogen mineralized in soils under anaerobic incubation condition were related to soil pH.The δ 15N of mineralizable N in acid soils was lower but that in neutral and calcareous soils was higher compared with the δ 15N of total N in the soils.A variation tendence was also found in the δ 15N of amino-acid N in the hydrolysates of soils.The natural 15N abundance of fixed ammonium was higher than that of total N in most surface soils and other soil horizons,indicating that the increase of δ 15N in the soil borizons beneath subsurface horizon of some forest soils and acid paddy soils was related to the higher δ 15N value of fixed ammonium in the soil.

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

    Science.gov (United States)

    Vallet, Valérie; Masella, Michel

    2015-01-01

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

  6. Reduction in Ammonium Ions in Sludge Liquor

    Directory of Open Access Journals (Sweden)

    Eglė Šlajūtė

    2013-12-01

    Full Text Available Liquor rejected from the centrifugation of the digested sludge can contain the concentrations of ammonium ions up to 1750 mg/L. These loads are usually returned to the intake of wastewater treatment plants (WWTP without additional treatment and can have a negative impact on biological wastewater and/or sludge treatment processes, e.g. phosphorus and nitrogen removal. This article deals with the use of naturally obtained sorbent, zeolite, in batch and column test procedure for removing ammonium from the rejected liquor. This research study was carried out using different sizes of zeolite particles: 0.8–1.6 mm and 1.6–2.5 mm. The highest efficiency of ammonium removal (up to 98 % was achieved by applying the zeolite particles of 0.8–1.6 mm.Article in Lithuanian

  7. Growth, spectroscopic and physicochemical properties of bis mercury ferric chloride tetra thiocyanate: A nonlinear optical crystal

    Science.gov (United States)

    Ramesh, V.; Shihabuddeen Syed, A.; Jagannathan, K.; Rajarajan, K.

    2013-05-01

    Single crystal of bis mercury ferric chloride tetra thiocyanate [Hg2FeCl3(SCN)4; (MFCTC)] was grown from ethanol-water (3:1) mixed solvent using slow evaporation solvent technique (SEST) for the first time. The cell parameters of the grown crystal were confirmed by single crystal XRD. The coordination of transition metal ions with the SCN ligand is well-identified using FT-IR spectral analysis. The chemical composition of MFCTC was confirmed using CHNS elemental test. The ESR spectral profile of MFCTC was recorded from 298 K to 110 K, which strongly suggests the incorporation of Fe3+ ion and its environment with respect to SCN ligand. The HPLC chromatogram of MFCTC highlights the purity of the compound. The UV-Vis-NIR studies revealed the ultra violet cut-off wavelength of MFCTC in ethanol as 338 nm. The dielectric constant and dielectric loss of the sample were studied as a function of frequency and temperature. The TGA-DTA and DSC thermal analysis show that the sample is thermally stable up to 234.31 °C, which is comparatively far better than the thermal stability of Hg3CdCl2(SCN)6; (171.3 °C) and other metal-organic coordination complex crystals such as CdHg(SCN)4 (198.5 °C), Hg(N2H4CS)4Mn(SCN)4 (199.06 °C) and Hg(N2H4CS)4Zn(SCN)4 (185 °C). The SHG conversion efficiency of MFCTC is found to be higher than KDP.

  8. Occupational Exposure in Ammonium Phosphate Fertilizer Plants

    International Nuclear Information System (INIS)

    Occupational exposures and activity concentrations have been assessed in two industrial plants producing mono-ammonium phosphate and di-ammonium phosphate fertilizers, located in south-western Spain. The annual effective doses received by the workers are below 1 mSv/a, with the contribution from external exposure being similar to that from internal exposure. The dose contribution from inhalation of dust has been estimated to be about 0.12 mSv/a, while the 222Rn concentrations inside the plants are of no concern. Consequently, no additional radiation protection measures need to be taken to protect the workers in these facilities. (author)

  9. Main Factors Effecting Anaerobic Ammonium Oxidation

    Institute of Scientific and Technical Information of China (English)

    YANG Xiao-fei

    2014-01-01

    Anaerobic Ammonium Oxidation (ANAMMOX) drew more attentions because of its denitrification in wastewater with low carbon resource. The external conditions of ANAMMOX are relatively harsh,however this reaction does not require the participation of oxygen and organics. So the research and technology development of ANAMMOX has the significance of sustainable development.In this paper, the main influencing factors of ANAMMOX were summarized,Combined with recent research status of ANAMMOX technology, the development trend of the anaerobic ammonium oxidation technology was prospected.

  10. On the evaporation of ammonium sulfate solution

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-07-16

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

  11. On the evaporation of ammonium sulfate solution.

    Science.gov (United States)

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

    2009-11-10

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

  12. Mechanism and regulation of peroxidase-catalyzed nitric oxide consumption in physiological fluids: critical protective actions of ascorbate and thiocyanate.

    Science.gov (United States)

    Rees, Martin D; Maiocchi, Sophie L; Kettle, Anthony J; Thomas, Shane R

    2014-07-01

    Catalytic consumption of nitric oxide (NO) by myeloperoxidase and related peroxidases is implicated as playing a key role in impairing NO bioavailability during inflammatory conditions. However, there are major gaps in our understanding of how peroxidases consume NO in physiological fluids, in which multiple reactive enzyme substrates and antioxidants are present. Notably, ascorbate has been proposed to enhance myeloperoxidase-catalyzed NO consumption by forming NO-consuming substrate radicals. However, we show that in complex biological fluids ascorbate instead plays a critical role in inhibiting NO consumption by myeloperoxidase and related peroxidases (lactoperoxidase, horseradish peroxidase) by acting as a competitive substrate for protein-bound redox intermediates and by efficiently scavenging peroxidase-derived radicals (e.g., urate radicals), yielding ascorbyl radicals that fail to consume NO. These data identify a novel mechanistic basis for how ascorbate preserves NO bioavailability during inflammation. We show that NO consumption by myeloperoxidase Compound I is significant in substrate-rich fluids and is resistant to competitive inhibition by ascorbate. However, thiocyanate effectively inhibits this process and yields hypothiocyanite at the expense of NO consumption. Hypothiocyanite can in turn form NO-consuming radicals, but thiols (albumin, glutathione) readily prevent this. Conversely, where ascorbate is absent, glutathione enhances NO consumption by urate radicals via pathways that yield S-nitrosoglutathione. Theoretical kinetic analyses provide detailed insights into the mechanisms by which ascorbate and thiocyanate exert their protective actions. We conclude that the local depletion of ascorbate and thiocyanate in inflammatory microenvironments (e.g., due to increased metabolism or dysregulated transport) will impair NO bioavailability by exacerbating peroxidase-catalyzed NO consumption. PMID:24704973

  13. Determination of thiocyanate (biomarkers of ETS) and other inorganic ions in human nasal discharge samples using ion chromatography.

    Science.gov (United States)

    Narkowicz, Sylwia; Polkowska, Żaneta; Marć, Mariusz; Simeonov, Vasil; Namieśnik, Jacek

    2013-10-01

    Environmental tobacco smoke (ETS) is a mixture of air and tobacco smoke containing more than 4000 chemical substances. In view of the health risks of many of these substances, studies are needed to determine biomarkers of exposure to ETS constituents in people who actively or passively are exposed to the toxic compounds. The methodologies for determining most biomarkers from saliva, urine and blood samples are known, but methods for analyzing these compounds in nasal discharges are not available. The objective of this work was to develop an analytical procedure for the determination of thiocyanate and other biomarker compounds in samples of nasal discharge using ion chromatography.

  14. Combined effects of perchlorate, thiocyanate, and iodine on thyroid function in the National Health and Nutrition Examination Survey 2007–08

    Energy Technology Data Exchange (ETDEWEB)

    Steinmaus, Craig, E-mail: craigs@berkeley.edu [Office of Environmental Health Hazard Assessment, California Environmental Protection Agency, 1515 Clay St. 16th Floor, Oakland, CA 94612 (United States); Miller, Mark D., E-mail: ucsfpehsumiller@gmail.com [Office of Environmental Health Hazard Assessment, California Environmental Protection Agency, 1515 Clay St. 16th Floor, Oakland, CA 94612 (United States); Cushing, Lara, E-mail: lara.cushing@berkeley.edu [Energy and Resources Group, 310 Barrows Hall, University of California, Berkeley, CA 93720-3050 (United States); Blount, Benjamin C., E-mail: bkb3@cdc.gov [Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, 4770 Buford Highway, NE, Mail Stop F47, Atlanta, GA (United States); Smith, Allan H., E-mail: ahsmith@berkeley.edu [Arsenic Health Effects Research Group, 1950 Addison St., Suite 204, University of California, Berkeley, CA 94704 (United States)

    2013-05-15

    Perchlorate, thiocyanate, and low iodine intake can all decrease iodide intake into the thyroid gland. This can reduce thyroid hormone production since iodide is a key component of thyroid hormone. Previous research has suggested that each of these factors alone may decrease thyroid hormone levels, but effect sizes are small. We hypothesized that people who have all three factors at the same time have substantially lower thyroid hormone levels than people who do not, and the effect of this combined exposure is substantially larger than the effects seen in analyses focused on only one factor at a time. Using data from the 2007–2008 National Health and Nutrition Examination Survey, subjects were categorized into exposure groups based on their urinary perchlorate, iodine, and thiocyanate concentrations, and mean serum thyroxine concentrations were compared between groups. Subjects with high perchlorate (n=1939) had thyroxine concentrations that were 5.0% lower (mean difference=0.40 μg/dl, 95% confidence interval=0.14–0.65) than subjects with low perchlorate (n=2084). The individual effects of iodine and thiocyanate were even smaller. Subjects with high perchlorate, high thiocyanate, and low iodine combined (n=62) had thyroxine concentrations 12.9% lower (mean difference=1.07 μg/dl, 95% confidence interval=0.55–1.59) than subjects with low perchlorate, low thiocyanate, and adequate iodine (n=376). Potential confounders had little impact on results. Overall, these results suggest that concomitant exposure to perchlorate, thiocyanate, and low iodine markedly reduces thyroxine production. This highlights the potential importance of examining the combined effects of multiple agents when evaluating the toxicity of thyroid-disrupting agents. -- Highlights: ► Recent data suggest that essentially everyone in the US is exposed to perchlorate. ► Perchlorate exposure may be associated with lower thyroid hormone levels. ► Some groups may be more susceptible to

  15. Combined effects of perchlorate, thiocyanate, and iodine on thyroid function in the National Health and Nutrition Examination Survey 2007–08

    International Nuclear Information System (INIS)

    Perchlorate, thiocyanate, and low iodine intake can all decrease iodide intake into the thyroid gland. This can reduce thyroid hormone production since iodide is a key component of thyroid hormone. Previous research has suggested that each of these factors alone may decrease thyroid hormone levels, but effect sizes are small. We hypothesized that people who have all three factors at the same time have substantially lower thyroid hormone levels than people who do not, and the effect of this combined exposure is substantially larger than the effects seen in analyses focused on only one factor at a time. Using data from the 2007–2008 National Health and Nutrition Examination Survey, subjects were categorized into exposure groups based on their urinary perchlorate, iodine, and thiocyanate concentrations, and mean serum thyroxine concentrations were compared between groups. Subjects with high perchlorate (n=1939) had thyroxine concentrations that were 5.0% lower (mean difference=0.40 μg/dl, 95% confidence interval=0.14–0.65) than subjects with low perchlorate (n=2084). The individual effects of iodine and thiocyanate were even smaller. Subjects with high perchlorate, high thiocyanate, and low iodine combined (n=62) had thyroxine concentrations 12.9% lower (mean difference=1.07 μg/dl, 95% confidence interval=0.55–1.59) than subjects with low perchlorate, low thiocyanate, and adequate iodine (n=376). Potential confounders had little impact on results. Overall, these results suggest that concomitant exposure to perchlorate, thiocyanate, and low iodine markedly reduces thyroxine production. This highlights the potential importance of examining the combined effects of multiple agents when evaluating the toxicity of thyroid-disrupting agents. -- Highlights: ► Recent data suggest that essentially everyone in the US is exposed to perchlorate. ► Perchlorate exposure may be associated with lower thyroid hormone levels. ► Some groups may be more susceptible to

  16. Thiocyanate ligands as crucial elements for regeneration and photo-degradation in TiO{sub 2} vertical bar dye vertical bar CuI solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Sirimanne, P.M. [Hahn-Meitner-Institut, Department Solare Energetik, Glienicker Str. 100, Alemania 14109 Berlin (Germany); Tributsch, H. [Hahn-Meitner-Institut, Department Solare Energetik, Glienicker Str. 100, Alemania 14109 Berlin (Germany)]. E-mail: tributsch@hmi.de

    2006-09-10

    Size control of CuI grains and thus better-matched interfaces were observed in the presence of crystal growth inhibitors in the CuI coating solution for TiO{sub 2} vertical bar dye vertical bar CuI solar cells. Evidence is given that these growth inhibitor molecules simultaneously act as an electron transfer mediator between the CuI and dye molecules via thiocyanate bridges. A reverse reaction of injected electrons from TiO{sub 2} nanoparticles electrochemically inactivates the thiocyanate electron transfer bridge in the illuminated cells causing photo-degradation.

  17. Al(HSO_4)_3/silica gel as a novel catalytic system for the ring opening of epoxides with thiocyanate anion under solvent-free conditions

    Institute of Scientific and Technical Information of China (English)

    Ali; Reza; Kiasat; Arash; Mouradzadegun; Somayeh; Elahi; Mehdi; Fallah-Mehrjardi

    2010-01-01

    For the first time,metal hydrogen sulfates and phosphates/silica gel have been studied as efficient and powerful solid acid catalysts in the ring opening of epoxides with thiocyanate anion.The most significant result was obtained by Al(HSO_4)_3/SiO_2 which afforded the corresponding β-hydroxy thiocyanates under mild reaction conditions and in very short reaction times.The cheapness, availability of the catalyst,ease of procedure and work-up make this method attractive for the organic synthesis.

  18. 76 FR 47238 - Ammonium Nitrate From Russia

    Science.gov (United States)

    2011-08-04

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

  19. 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... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ammonium alginate. 184.1133 Section 184.1133 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD...

  20. Topaz concentrate desiliconization with ammonium bifluoride

    OpenAIRE

    Andreev, V. A.; Buynovskiy, A. S.; Andreev, Artyom Andreevich; Dyachenko, Alexander Nikolaevich

    2007-01-01

    Fluoridizing agent for the process of topaz concentrate desiliconization has been selected, topaz thermodynamic potentials have been appraised, thermodynamic probabilities of fluorination reaction of topaz concentrate main constituents have been calculated. The results of studying the concentrate desiliconization process with ammonium bifluoride by the methods of thermogravimetry, RFA, microphotography are presented

  1. 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 Associ

  2. 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.

  3. 76 FR 46907 - Ammonium Nitrate Security Program

    Science.gov (United States)

    2011-08-03

    ... comments. SUMMARY: This proposed rule would implement anti-terrorism measures to better secure the homeland... purpose of preventing the use of ammonium nitrate in an act of terrorism. This proposed rule seeks comment... Administration POC Point of Contact QATT Qualified Anti-Terrorism Technology RFA Regulatory Flexibility...

  4. Kinetic analysis of phenol, thiocyanate and ammonia-nitrogen removals in an anaerobic-anoxic-aerobic moving bed bioreactor system

    Energy Technology Data Exchange (ETDEWEB)

    Sahariah, Biju Prava [Centre for the Environment, Indian Institute of Technology Guwahati, Assam 781039 (India); Chakraborty, Saswati, E-mail: chakraborty_saswati@hotmail.com [Department of Civil Engineering, Indian Institute of Technology Guwahati, Assam 781039 (India)

    2011-06-15

    A simulated wastewater containing phenol (2500 mg/L), thiocyanate and ammonia-nitrogen (500 mg/L) was treated in an anaerobic (R1)-anoxic (R2)-aerobic (R3) moving bed biofilm reactor system at different hydraulic retention time (HRT) intervals (total HRT 3-8 days, R1: 1.5-4 days; R2: 0.75-2 days and R3: 0.75-2 days) and feed thiocyanate (SCN{sup -}) concentrations (110-600 mg/L) to determine substrate removal kinetics. In R1, phenol and COD reduction and specific methanogenic activity were inhibited due to the increase of SCN{sup -} in feed. Bhatia et al. model having inbuilt provision of process inhibition described the kinetics of COD and phenol utilization with maximum utilization rates of 0.398 day{sup -1} and 0.486 day{sup -1}, respectively. In R2 and R3 modified Stover-Kincannon model was suitable to describe substrate utilization. In R2 respective maximum SCN{sup -}, phenol, COD and NO{sub 3}{sup -}N utilization rates were 0.23, 5.28, 37.7 and 11.82 g/L day, respectively. In aerobic reactor R3, COD, SCN{sup -} and NH{sub 4}{sup +}-N removal rates were, respectively, 10.53, 1.89, and 2.17 g/L day. The minimum total HRT of three-stage system was recommended as 4 days.

  5. Kinetic analysis of phenol, thiocyanate and ammonia-nitrogen removals in an anaerobic-anoxic-aerobic moving bed bioreactor system

    International Nuclear Information System (INIS)

    A simulated wastewater containing phenol (2500 mg/L), thiocyanate and ammonia-nitrogen (500 mg/L) was treated in an anaerobic (R1)-anoxic (R2)-aerobic (R3) moving bed biofilm reactor system at different hydraulic retention time (HRT) intervals (total HRT 3-8 days, R1: 1.5-4 days; R2: 0.75-2 days and R3: 0.75-2 days) and feed thiocyanate (SCN-) concentrations (110-600 mg/L) to determine substrate removal kinetics. In R1, phenol and COD reduction and specific methanogenic activity were inhibited due to the increase of SCN- in feed. Bhatia et al. model having inbuilt provision of process inhibition described the kinetics of COD and phenol utilization with maximum utilization rates of 0.398 day-1 and 0.486 day-1, respectively. In R2 and R3 modified Stover-Kincannon model was suitable to describe substrate utilization. In R2 respective maximum SCN-, phenol, COD and NO3-N utilization rates were 0.23, 5.28, 37.7 and 11.82 g/L day, respectively. In aerobic reactor R3, COD, SCN- and NH4+-N removal rates were, respectively, 10.53, 1.89, and 2.17 g/L day. The minimum total HRT of three-stage system was recommended as 4 days.

  6. 40 CFR 721.4095 - Quaternary ammonium alkyltherpropyl trialkylamine halides.

    Science.gov (United States)

    2010-07-01

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

  7. 21 CFR 184.1296 - Ferric ammonium citrate.

    Science.gov (United States)

    2010-04-01

    ... citrate (iron (III) ammonium citrate) is prepared by the reaction of ferric hydroxide with citric acid, followed by treatment with ammonium hydroxide, evaporating, and drying. The resulting product occurs in two forms depending on the stoichiometry of the initial reactants. (1) Ferric ammonium citrate (iron...

  8. 40 CFR 721.10099 - Dialkyl dimethyl ammonium carbonate (generic).

    Science.gov (United States)

    2010-07-01

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

  9. Comments on the paper: Synthesis growth and characterization of copper mercury thiocyanate crystal [Indian J Pure & App Phys 49 (2011) 340-343

    OpenAIRE

    Srinivasan, Bikshandarkoil R.

    2015-01-01

    The unit cell parameters, infrared and UV-Vis spectral data reported in the paper by Vijayabhaskaran et al (Indian J Pure & App Phys 49 (2011) 340-343) cannot belong to the colourless crystalline compound formulated as copper mercury thiocyanate CuHg(SCN)4 as claimed by the authors.

  10. Surface studies on bimetallic thiocyanate ligand based single crystals of MnHg(SCN) 4, CdHg(SCN) 4 and ZnCd(SCN) 4

    Science.gov (United States)

    Rajesh Kumar, T.; Jeyasekaran, R.; Ravi Kumar, S. M.; Vimalan, M.; Sagayaraj, P.

    2010-12-01

    Bimetallic SCN ligand based single crystals of manganese mercury thiocyanate (MMTC), cadmium mercury thiocyanate (CMTC) and zinc cadmium thiocyanate (ZCTC) are grown by slow solvent evaporation technique. The growth mechanism and surface features are investigated by optical microscopic techniques such as scanning electron microscopy (SEM) and atomic force microscopy (AFM). The laser induced surface damage measurements were carried out using a Q-switched Nd:YAG laser at 1064 nm with laser beam of 1.0 Hz and pulse duration 25 ps. The laser damage threshold values of MMTC, CMTC and ZCTC are found to be 15.9, 22.9 and 19.7 GW/cm 2, respectively. The SEM analysis of MMTC reveals the formation of elongated dendrite growth pattern caused by the fluctuations of Mn and Hg metal ligands when thiocyanate (SCN) bridges them. The etching study indicates the occurrence of different types of etch pit patterns like terraced triangles, pillars, pyramids and rods. The AFM images confirm the formation of three major hillocks with cavities in MMTC. The measured roughness values for CMTC crystal are very much lower than that of MMTC.

  11. A one-dimensional CdII coordination polymer constructed from 4-(dimethylamino)pyridinium-1-acetate ligands and thiocyanate coordination bridges.

    Science.gov (United States)

    Wang, Hui-Ting; Zhou, Lin

    2015-07-01

    A new cadmium-thiocyanate complex, namely catena-poly[1-carboxymethyl-4-(dimethylamino)pyridinium [cadmium(II)-tri-μ-thiocyanato-κ(4)N:S;κ(2)S:N] [[[4-(dimethylamino)pyridinium-1-acetate-κ(2)O,O']cadmium(II)]-di-μ-thiocyanato-κ(2)N:S;κ(2)S:N

  12. A Selective Membrane Electrode for Thiocyanate Ion Based on a Bis-taurine-salicylic Binuclear Copper(Ⅱ) Complex as Ionophore

    Institute of Scientific and Technical Information of China (English)

    王福昌; 柴雅琴; 袁若; 陈春华; 戴建远; 徐岚

    2005-01-01

    The response characteristics of a new potentiometric membrane electrode with unique selectivity towards thiocyanate ion were reported. The electrode was prepared by incorporating bis-taurine-salicylic binuclear copper(Ⅱ) complex into a plasticized PVC-membrane. The resulting electrode exhibits anti-Hofmeister selectivity sequence: SCN->I-> ClO4- >Sal-> NO3- > NO2- >Br->Cl-> SO3- > SO42- and a near-Nernstian potential linear range for thiocyanate from 1.0×10-1 to 1.0× 10-6 mol·L-1 with a detection limit of 8.0× 10-7 mol·L-1 and a slope of - 56.5 mV/PCSCN- in phosphate buffer solution of pH 5.0 at 20 ℃. The UV/Vis spectra, IR spectroscopy and AC impedance studies showed that the excellent selectivity to thiocyanate was related to the unique interaction between the central metal and the analyte and a steric effect associated with the structure of the carrier. The electrode was successfully applied to the determination of thiocyanate in waste water and human urine samples.

  13. Detonation Properties of Ammonium Dinitramide (ADN)

    Science.gov (United States)

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

    1999-06-01

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

  14. Development of technology for ammonium nitrate dissociation process

    International Nuclear Information System (INIS)

    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

  15. Probing the early stages of salt nucleation—Experimental and theoretical investigations of sodium/potassium thiocyanate cluster anions

    Science.gov (United States)

    Deng, S. H. M.; Kong, Xiang-Yu; Wang, Xue-Bin

    2015-01-01

    Due to the fast solvent evaporation in electrospray ionization (ESI), the concentration of initially dilute electrolyte solutions rapidly increases to afford the formation of supersaturated droplets and generation of various pristine anhydrous salt clusters in the gas phase. The size, composition, and charge distributions of these clusters, in principle, witness the nucleation evolution in solutions. Herein, we report a microscopic study on the initial stage of nucleation and crystallization of sodium/potassium thiocyanate salt solutions simulated in the ESI process. Singly charged M x (SCN)x + 1 - , doubly charged M y (SCN)y + 2 2 - (M = Na, K), and triply charged K z (SCN)z + 3 3 - anion clusters (x, y, and z stand for the number of alkali atoms in the singly, doubly, and triply charged clusters, respectively) were produced via electrospray of the corresponding salt solutions and were characterized by negative ion photoelectron spectroscopy (NIPES). The vertical detachment energies (VDEs) of these sodium/potassium thiocyanate cluster anions were obtained, and theoretical calculations were carried out for the sodium thiocyanate clusters in assisting spectral identification. The measured VDEs of singly charged anions M x (SCN)x + 1 - (M = Na and K) demonstrate that they are superhalogen anions. The existence of doubly charged anions M y (SCN)y + 2 2 - (y = 2x, x ≥ 4 and 3 for M = Na and K, respectively) and triply charged anions K z (SCN)z + 3 3 - (z = 3x, x ≥ 6) was initially discovered from the photoelectron spectra for those singly charged anions of M x (SCN)x + 1 - with the same mass-to-charge ratio (m/z), and later independently confirmed by the observation of their distinct mass spectral distributions and by taking their NIPE spectra for those pure multiply charged anions with their m/z different from the singly charged species. For large clusters, multiply charged clusters were found to become preferred, but at higher temperatures, those multiply charged

  16. Fluorescence spectroscopic studies of (acetamide + sodium/potassium thiocyanates) molten mixtures: composition and temperature dependence.

    Science.gov (United States)

    Guchhait, Biswajit; Gazi, Harun Al Rasid; Kashyap, Hemant K; Biswas, Ranjit

    2010-04-22

    Steady state and time-resolved fluorescence spectroscopic techniques have been used to explore the Stokes' shift dynamics and rotational relaxation of a dipolar solute probe in molten mixtures of acetamide (CH(3)CONH(2)) with sodium and potassium thiocyanates (Na /KSCN) at T approximately 318 K and several other higher temperatures. The dipolar solute probe employed for this study is coumarin 153 (C153). Six different fractions (f) of KSCN of the following ternary mixture composition, 0.75 CH(3)CONH(2) + 0.25[(1 - f)NaSCN + fKSCN], have been considered. The estimated experimental dynamic Stokes' shift for these systems ranges between 1800 and 2200 cm(-1) (+/-250 cm(-1)), which is similar to what has been observed with the same solute probe in several imidazolium cation based room temperature ionic liquids (RTIL) and in pure amide solvents. Interestingly, this range of estimated Stokes' shift, even though not corresponding to the megavalue of static dielectric constant reported in the literature for a binary mixture of molten CH(3)CONH(2) and NaSCN, exhibits a nonmonotonic KSCN concentration dependence. The magnitudes of the dynamic Stokes' shift detected in the present experiments are significantly less than the estimated ones, as nearly 40-60% of the total shift is missed due to the limited time resolution employed (full-width at half-maximum of the instrument response function approximately 70 ps). The solvation response function, constructed from the detected shifts in these systems, exhibits triexponential decay with the fastest time constant (tau(1)) in the 10-20 ps range, which might be much shorter if measured with a better time resolution. The second time constant (tau(2)) lies in the 70-100 ps range, and the third one (tau(3)) ranges between 300 and 800 ps. Both these time constants (tau(2) and tau(3)) show alkali metal ion concentration dependence and exhibit viscosity decoupling at higher viscosity in the NaSCN-enriched region. Time dependent rotational

  17. Growth, optical, electrical and photoconductivity studies of a novel nonlinear optical single crystal: Mercury cadmium chloride thiocyanate

    Science.gov (United States)

    Kumar, S. M. Ravi; Selvakumar, S.; Sagayaraj, P.; Anbarasi, A.

    2015-02-01

    SCN- ligand based organometallic non-linear optical mercury cadmium chloride thiocyanate (MCCTC) crystals are grown from water plus methanol mixed solvent by slow evaporation technique. The grown crystals are confirmed by single crystal X-ray diffraction analysis which reveals that the MCCTC belongs to rhombohedral system with R3c space group. MCCTC exhibits a SHG efficiency which is nearly 17 times more than that of KDP. The dielectric constant, dielectric loss measurements of the sample have been carried out for different frequencies (100 Hz to 5 MHz) and, temperatures (308 to 388 K) and the results are discussed. Photoconductivity study confirms that the title compound possesses negative photoconducting nature. The surface morphology of MCCTC was also investigated

  18. A comparative study of pure and potassium doped cadmium mercury thiocyanate single crystals grown in silica gel

    Energy Technology Data Exchange (ETDEWEB)

    Kumari, P.N.S. [Department of Physics, Auxilium College, Vellore (India); Margaret, M.B. [Department of Physics, Arignar Anna Govt. College for Women, Walajapet (India); Kalainathan, S. [School of Science and Humanities, VIT University, Vellore (India)

    2009-02-15

    Pure and potassium doped cadmium mercury thiocyanate single crystals have been obtained from silica gel by the process of diffusion. The X-ray diffraction studies reveal the crystal lattice of both pure and doped crystals to be tetragonal. The crystalline perfection of the grown crystals were investigated by high resolution X-ray diffraction analysis and the quality of the crystals are found to be extremely good. Transmission and Fourier transform infrared spectra were recorded for the grown crystals. The TG/DTA analyses show that the crystals are highly thermally stable. The mechanical strength of the crystals were studied by Vickers microhardness test and a study of their second harmonic generation efficiency in comparison with urea has been made by performing Kurtz powder test. (copyright 2009 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  19. Linear and nonlinear optical, mechanical, electrical and surface studies of a novel nonlinear optical crystal - Manganese mercury thiocyanate (MMTC)

    Science.gov (United States)

    Josephine Usha, R.; Sagayaraj, P.; Joseph, V.

    2014-12-01

    The highly efficient nonlinear optical single crystal of manganese mercury thiocyanate has been grown from slow evaporation solvent technique. The second harmonic generation and optical transmittance of the grown crystal are studied by Kurtz and Perry powder technique and spectroscopic absorbance spectrum. Mechanical behaviour is analyzed using Vickers microhardness test. The dielectric response of the grown crystal is studied as a function of the temperature and the results are discussed. Further, electronic properties such as plasma energy, Penngap, Fermi energy and electronic polarizability are evaluated. Third order nonlinear optical studies are performed using by single beam Z-scan technique using Nd:YAG laser and parameters such as nonlinear refractive index n2, absorption co-efficient β and nonlinear optical susceptibility χ(3) are evaluated for the grown crystal. The surface of the grown crystal is analyzed with field emission scanning electron microscope and atomic force microscope analyses.

  20. A novel cobalt (I) coordination polymer with mixed thiocyanate and quinoline ligands: crystal structure, magnetism and luminescent properties.

    Science.gov (United States)

    Li, Lei; Chen, Shuai; Zhou, Rui-Min; Bai, Yan; Dang, Dong-Bin

    2014-01-01

    A new Co(I) one-dimensional coordination polymer [Co(SCN)(ql)]n (ql=quinoline) (1) has been synthesized and characterized by IR, elemental analysis, TG technique and X-ray crystallography. Co(I) atom has a distorted trigonal pyramidal N2S2 (1) environment with two S atoms and one N atom from three μ-1,1,3-thiocyanate bridge ligands and one N atom from ql ligand. Two S atoms from two μ-1,1,3-SCN- bridging ligands bridge two centers to obtain bimetallic 4-membered ring. Adjacent 4-membered rings are linked by a pair of μ-1,1,3-SCN- bridging ligands to form a 1D stair-case like chain. The luminescent properties and magnetic properties of the polymer 1 were investigated in the solid state. PMID:24211622

  1. Chronic toxicity of diphenhydramine hydrochloride and erythromycin thiocyanate to Daphnia, Daphnia magna, in a continuous exposure test system

    Science.gov (United States)

    Meinertz, J.R.; Schreier, T.M.; Bernardy, J.A.; Franz, J.L.

    2010-01-01

    Diphenhydramine hydrochloride (DH; Benadryl TM, an over-the-counter antihistamine) and erythromycin thiocyanate (ET; a commonly used macrolide antibiotic) are pharmaceutical compounds whose chronic toxicity to Daphnia magna had not been characterized. Continuous exposure to DH concentrations about 5 times greater than the maximum reported environmental concentration of 0.023 lg/L for 21 days or to ET concentrations about 40 times the maximum reported environmental concentration of 6 (mu or u)g/L for 21 days did not significantly impact D. magna survival and production. In this study the no observable effect concentration for DH was 0.12 (mu or u)g/L and for ET was 248 (mu or u)g/L.

  2. Chronic toxicity of erythromycin thiocyanate to Daphnia magna in a flow-through, continuous exposure test system

    Science.gov (United States)

    Meinertz, J.R.; Schreier, T.M.; Bernardy, J.A.

    2011-01-01

    Approval of a new animal drug application for AQUAMYCIN 100?? (erythromycin thiocyanate; ET) to treat freshwater salmonid species with bacterial kidney disease is being pursued in the US. As part of the approval process, ETs impact on an aquatic environment had to be described in an environmental assessment. The environmental assessment was lacking data to characterize the effect ET would have on a chronically exposed aquatic invertebrate organism. A major step to fulfilling the environmental assessment was completed after conducting a comprehensive study continuously exposing Daphnia magna to ET for 21 days. Results indicated that the no observable effect concentration for ET was 179 ??g/L. ?? 2011 Springer Science+Business Media, LLC (outside the USA).

  3. Analysis of perchlorate, thiocyanate, nitrate and iodide in human amniotic fluid using ion chromatography and electrospray tandem mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Blount, Benjamin C. [Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA 30341 (United States)]. E-mail: bblount@cdc.gov; Valentin-Blasini, Liza [Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA 30341 (United States)

    2006-05-10

    Because of health concerns surrounding in utero exposure to perchlorate, we developed a sensitive and selective method for quantifying iodide, as well as perchlorate and other sodium-iodide symporter (NIS) inhibitors in human amniotic fluid using ion chromatography coupled with electrospray ionization tandem mass spectrometry. Iodide and NIS inhibitors were quantified using a stable isotope-labeled internal standards (Cl{sup 18}O{sub 4} {sup -}, S{sup 13}CN{sup -} and {sup 15}NO{sub 3} {sup -} with excellent assay accuracy of 100%, 98%, 99%, 95% for perchlorate, thiocyanate, nitrate and iodide, respectively, in triplicate analysis of spiked amniotic fluid sample). Excellent analytical precision (<5.2% RSD for all analytes) was found when amniotic fluid quality control pools were repetitively analyzed for iodide and NIS-inhibitors. Selective chromatography and tandem mass spectrometry reduced the need for sample cleanup, resulting in a rugged and rapid method capable of routinely analyzing 75 samples/day. Analytical response was linear across the physiologically relevant concentration range for the analytes. Analysis of a set of 48 amniotic fluid samples identified the range and median levels for perchlorate (0.057-0.71, 0.18 {mu}g/L), thiocyanate (<10-5860, 89 {mu}g/L), nitrate (650-8900, 1620 {mu}g/L) and iodide (1.7-170, 8.1 {mu}g/L). This selective, sensitive, and rapid method will help assess exposure of the developing fetus to low levels of NIS-inhibitors and their potential to inhibit thyroid function.

  4. Review:Anaerobic ammonium oxidation for treatment of ammonium-rich wastewaters

    Institute of Scientific and Technical Information of China (English)

    Lei ZHANG; Ping ZHENG; Chongojian TANG; Ren-cun JIN

    2008-01-01

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

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

    Science.gov (United States)

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

    2016-07-01

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

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

    Science.gov (United States)

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

    2015-09-01

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

  7. Quaternary Ammonium Polyethyleneimine: Antibacterial Activity Ira

    International Nuclear Information System (INIS)

    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.

  8. Reassimilation of ammonium in Lotus japonicus.

    Science.gov (United States)

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

    2014-10-01

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

  9. Ammonium nitrate: a promising rocket propellant oxidizer

    Science.gov (United States)

    Oommen; Jain

    1999-06-30

    Ammonium nitrate (AN) is extensively used in the area of fertilizers and explosives. It is present as the major component in most industrial explosives. Its use as an oxidizer in the area of propellants, however, is not as extensive as in explosive compositions or gas generators. With the growing demand for environmental friendly chlorine free propellants, many attempts have been made of late to investigate oxidizers producing innocuous combustion products. AN, unlike the widely used ammonium perchlorate, produces completely ecofriendly smokeless products. Besides, it is one of the cheapest and easily available compounds. However, its use in large rocket motors is restricted due to some of its adverse characteristics like hygroscopicity, near room temperature phase transformation involving a volume change, and low burning rate (BR) and energetics. The review is an attempt to consolidate the information available on the various issues pertaining to its use as a solid propellant oxidizer. Detailed discussions on the aspects relating to phase modifications, decomposition chemistry, and BR and energetics of AN-based propellants, are presented. To make the review more comprehensive brief descriptions of the history, manufacture, safety, physical and chemical properties and various other applications of the salt are also included. Copyright 1999 Elsevier Science B.V.

  10. Studies on the electrical, linear and nonlinear optical properties of Manganese mercury thiocyanate bis-dimethyl sulfoxide, an efficient NLO crystal

    Energy Technology Data Exchange (ETDEWEB)

    Joseph, Ginson P. [Department of Physics, Loyola College, Chennai 600 034 (India); Melikechi, N. [Centre for Research and Education in Optical Sciences and Applications, Department of Physics and Pre-Engineering, Delaware State University, Dover, DE 19901 (United States); Philip, Jacob [Department of instrumentation, Cochin University of Science and Technology (India); Madhavan, J. [Department of Physics, Loyola College, Chennai 600 034 (India); Sagayaraj, P. [Department of Physics, Loyola College, Chennai 600 034 (India)], E-mail: psagayaraj@hotmail.com

    2009-02-28

    Manganese mercury thiocyanate bis-dimethyl sulfoxide (MMTD), a novel organo-metallic nonlinear optical (NLO) crystal, was grown by a slow evaporation technique over a period of 30 days. The grown crystal was subjected to single crystal X-ray diffraction to determine the unit cell parameters. The optical properties of MMTD were investigated by UV-Vis-NIR, FTIR and FT-Raman spectroscopic techniques. The second harmonic generation (SHG) efficiency of the sample was measured using a Q-switched, mode-locked Nd:YAG laser and the results were compared with urea and manganese mercury thiocyanate (MMTC). The thermal parameters, such as the thermal diffusivity ({alpha}), thermal effusivity (e), thermal conductivity (k) and heat capacity (c{sub p}) of MMTD were measured by the photopyroelectric (PPE) technique and the results are discussed. The dielectric response and mechanical properties of MMTD have also been investigated and reported.

  11. A two-dimensional cadmium(II) coordination polymer based on 1-cyanomethyl-4-aza-1-azoniabicyclo[2.2.2]octane and thiocyanate ligands.

    Science.gov (United States)

    Wang, Hui-Ting; Li, Qiang; Zhou, Lin

    2015-09-01

    A cadmium-thiocyanate complex, poly[(1-cyanomethyl-4-aza-1-azoniabicyclo[2.2.2]octane-κ(4)N)octakis-μ2-thiocyanato-κ(8)N:S;κ(8)S:N-tricadmium(II)], [Cd3(C8H14N3)2(NCS)8]n, was synthesized by the reaction of 1-cyanomethyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride, cadmium nitrate tetrahydrate and potassium thiocyanide in aqueous solution. In the crystal structure, there are two independent types of Cd(II) cation (one on a centre of inversion and one in a general position) and both are in distorted octahedral coordination environments, coordinated by N and S atoms from different ligands. Neighbouring Cd(II) cations are linked together by thiocyanate bridges to form a two-dimensional network. Hydrogen-bonding interactions are involved in the formation of a three-dimensional supramolecular network. PMID:26322607

  12. Acrylonitrile-14C metabolism in rats: effect of the route of administration on the elimination of thiocyanate and other radioactive metabolites in urine and feces

    International Nuclear Information System (INIS)

    In Wistar rats, the elimination of the sum of radioactive metabolites of acrylonitrile-14C was not markedly influenced by the route of acrylonitrile administration. The elimination of thiocyanate, however, was significantly higher after oral (23% of the dose) than after intraperitoneal (4%), subcutaneous (4.6%), or intravenous (1.2%) administrations. The elimination of the sum of radioactive metabolites was highest in the first 4 hours after acrylonitrile administration and rapidly decreased whereas the excretion of thiocyanate reached the maximum between hours 8 and 14 after oral or intraperitoneal administration. Less than 1% of the radioactivity of the acrylonitrile-14C dose was eliminated in feces irrespective of the route of administration. (author)

  13. Preparation of 2'-13C-L-Histidine Starting from 13C-Thiocyanate: Synthetic Access to Any Site-Directed Stable Isotope Enriched L-Histidine

    Directory of Open Access Journals (Sweden)

    Sarra Talab

    2014-01-01

    Full Text Available 1-Benzyl-2-(methylthio-imidazole-5-ketone is obtained in a few simple steps starting from thiocyanate and glycine amide (glycin. Subsequent treatment with diethyl phosphorocyanidate and functional group manipulations gives 1-benzyl-5-chloromethyl-imidazolium chloride. This compound is converted under mild O’Donnell conditions into the corresponding L-histidine derivative. After deprotection L-histidine is obtained in good yield and 99% enantiomeric excess. 2'-13C-L-Histidine has been obtained via this new scheme with high (99% 13C incorporation starting with commercially available 13C- thiocyanate. This synthetic scheme allows access to any isotopomer of L-histidine and many other biologically important imidazole derivatives.

  14. RNA extraction from various recalcitrant plant tissues with a cethyltrimethylammonium bromide-containing buffer followed by an acid guanidium thiocyanate-phenol-chloroform treatment.

    Science.gov (United States)

    Suzuki, Yuji; Mae, Tadahiko; Makino, Amane

    2008-07-01

    High-quality total RNA was extracted using a cethyltrimethylammonium bromide-containing buffer followed by an acid guanidium thiocyanate-phenol-chloroform treatment from recalcitrant plant tissues such as tree leaves (pine, Norway spruce, ginkgo, Japanese cedar, rose), flowers (rose, Lotus japonicus) and storage tissues (seeds of Lotus japonicus and rice, sweet potato tuber, banana fruit). This protocol greatly reduced the time required for RNA extraction.

  15. Electric field-induced hole transport in copper(i) thiocyanate (CuSCN) thin-films processed from solution at room temperature

    KAUST Repository

    Pattanasattayavong, Pichaya

    2013-01-01

    The optical, structural and charge transport properties of solution-processed films of copper(i) thiocyanate (CuSCN) are investigated in this work. As-processed CuSCN films of ∼20 nm in thickness are found to be nano-crystalline, highly transparent and exhibit intrinsic hole transporting characteristics with a maximum field-effect mobility in the range of 0.01-0.1 cm2 V-1 s-1. © 2013 The Royal Society of Chemistry.

  16. Preparation of 2'-13C-L-Histidine Starting from 13C-Thiocyanate: Synthetic Access to Any Site-Directed Stable Isotope Enriched L-Histidine

    OpenAIRE

    Sarra Talab; Kamal Khalifa Taha; Johan Lugtenburg

    2014-01-01

    1-Benzyl-2-(methylthio)-imidazole-5-ketone is obtained in a few simple steps starting from thiocyanate and glycine amide (glycin). Subsequent treatment with diethyl phosphorocyanidate and functional group manipulations gives 1-benzyl-5-chloromethyl-imidazolium chloride. This compound is converted under mild O’Donnell conditions into the corresponding L-histidine derivative. After deprotection L-histidine is obtained in good yield and 99% enantiomeric excess. 2'-13C-L-Histidine has been obtai...

  17. 棒状硫氰液晶的合成与表征%Synthesis and Characterization of Rod-Shaped Thiocyanic Liquid Crystals

    Institute of Scientific and Technical Information of China (English)

    刘卫东; 伍勇

    2011-01-01

    Rod-shaped thiocyanic compounds based on a 4-benzoyloxy-biphenyl mesogen were prepared by nucleophilic substitution with a thiocyanic salt.The number of carbon atoms in one terminal alkyloxy chain was 6, 8 and 10.The mesomorphic properties of the synthesized compounds were characterized by means of polarized optical microscopy and differential scanning calorimeter.The results demonstrated that the thiocyanic compounds exhibited thermotropic smectic A and nematic phases.The isotropic point of the liquid crystals decreased with the increase in length of the terminal alkyloxy chain.%通过硫氰酸盐亲核取代反应合成了以苯甲酸联苯酯为液晶基元的硫氰棒状分子,一端尾链中的碳原子数为6、8和10.用偏光显微镜和差示扫描量热分析法对所合成的化合物进行了液晶相的表征,结果表明,这些硫氰化合物均表现出热致性近晶A相、向列相及尚未定性的液晶相M.随着尾链的增长,向列相温度区间变窄,清亮点降低.

  18. 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.

  19. Novel bimetallic thiocyanate-bridged Cu(II)-Hg(II) compounds-synthesis, X-Ray studies and magnetic properties

    Energy Technology Data Exchange (ETDEWEB)

    Machura, B., E-mail: basia@ich.us.edu.pl [Department of Crystallography, Institute of Chemistry, University of Silesia, 9th Szkolna St., 40-006 Katowice (Poland); Switlicka, A.; Zwolinski, P. [Department of Crystallography, Institute of Chemistry, University of Silesia, 9th Szkolna St., 40-006 Katowice (Poland); Mrozinski, J., E-mail: jmroz@wchuwr.chem.uni.wroc.pl [Faculty of Chemistry, Wroclaw University, F. Joliot-Curie 14 St., 50-383 Wroclaw (Poland); Kalinska, B. [Faculty of Chemistry, Wroclaw University, F. Joliot-Curie 14 St., 50-383 Wroclaw (Poland); Kruszynski, R., E-mail: rafal.kruszynski@p.lodz.pl [Department of X-Ray Crystallography and Crystal Chemistry, Institute of General and Ecological Chemistry, Technical University of Lodz, 116 Zeromski St., 90-924 Lodz (Poland)

    2013-01-15

    Seven novel heterobimetallic Cu/Hg polymers based on thiocyanate bridges have been synthesised and characterised by means of IR, EPR, magnetic measurements and single crystal X-Ray. Three of them, [Cu(pzH){sub 4}Hg(SCN){sub 4}]{sub n} (1) [Cu(indH){sub 4}Hg(SCN){sub 4}]{sub n} (2) and [Cu(ampy){sub 2}Hg(SCN){sub 4}]{sub n} (3), have one-dimensional coordination structure. Two compounds [Cu(pzH){sub 2}Hg(SCN){sub 4}]{sub n} (4) and [Cu(abzimH)Hg(SCN){sub 4}]{sub n} (5) form two-dimensional nets, whereas the complexes [Cu(pyCN){sub 2}Hg(SCN){sub 4}]{sub n} (6) and [Cu(pyCH(OH)(OMe)){sub 2}Hg(SCN){sub 4}]{sub n} (7) are three-dimensional coordination polymers. The chains of 1 are connected by the intermolecular N-H Bullet Bullet Bullet N hydrogen bonds to the three dimensional net. In 2 the N-H Bullet Bullet Bullet S hydrogen bonds link the polymeric chains to the two dimensional layer extending along crystallographic (0 0 1) plane. The polymeric chains of compound 3 are joined by the intermolecular N-H Bullet Bullet Bullet N and N-H Bullet Bullet Bullet S hydrogen bonds to the three dimensional net. The polymeric layers of 4 are connected by the intermolecular N-H Bullet Bullet Bullet N hydrogen bonds to the three dimensional net. - Graphical abstract: Novel bimetallic thiocyanate-bridged Cu(II)-Hg(II) compound-synthesis,X-Ray studies and magnetic properties. Highlights: Black-Right-Pointing-Pointer Novel heterobimetallic Cu/Hg coordination polymers were synthesised. Black-Right-Pointing-Pointer The multidimensional structures have been proved by single X-ray analysIs. Black-Right-Pointing-Pointer A variation in the crystalline architectures was observed depending on auxiliary ligands. Black-Right-Pointing-Pointer Magnetic measurements indicate weak exchange interaction between Cu(II) in the crystal lattices below 10 K.

  20. Thiocyanate complexes of uranium in multiple oxidation states: a combined structural, magnetic, spectroscopic, spectroelectrochemical, and theoretical study.

    Science.gov (United States)

    Hashem, Emtithal; Platts, James A; Hartl, František; Lorusso, Giulia; Evangelisti, Marco; Schulzke, Carola; Baker, Robert J

    2014-08-18

    A comprehensive study of the complexes A4[U(NCS)8] (A = Cs, Et4N, (n)Bu4N) and A3[UO2(NCS)5] (A = Cs, Et4N) is described, with the crystal structures of [(n)Bu4N]4[U(NCS)8]·2MeCN and Cs3[UO2(NCS)5]·O0.5 reported. The magnetic properties of square antiprismatic Cs4[U(NCS)8] and cubic [Et4N]4[U(NCS)8] have been probed by SQUID magnetometry. The geometry has an important impact on the low-temperature magnetic moments: at 2 K, μeff = 1.21 μB and 0.53 μB, respectively. Electronic absorption and photoluminescence spectra of the uranium(IV) compounds have been measured. The redox chemistry of [Et4N]4[U(NCS)8] has been explored using IR and UV-vis spectroelectrochemical methods. Reversible 1-electron oxidation of one of the coordinated thiocyanate ligands occurs at +0.22 V vs Fc/Fc(+), followed by an irreversible oxidation to form dithiocyanogen (NCS)2 which upon back reduction regenerates thiocyanate anions coordinating to UO2(2+). NBO calculations agree with the experimental spectra, suggesting that the initial electron loss of [U(NCS)8](4-) is delocalized over all NCS(-) ligands. Reduction of the uranyl(VI) complex [Et4N]3[UO2(NCS)5] to uranyl(V) is accompanied by immediate disproportionation and has only been studied by DFT methods. The bonding in [An(NCS)8](4-) (An = Th, U) and [UO2(NCS)5](3-) has been explored by a combination of DFT and QTAIM analysis, and the U-N bonds are predominantly ionic, with the uranyl(V) species more ionic that the uranyl(VI) ion. Additionally, the U(IV)-NCS ion is more ionic than what was found for U(IV)-Cl complexes. PMID:25072532

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

    Science.gov (United States)

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

  2. 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 hydro

  3. How to make a living from anaerobic ammonium oxidation

    NARCIS (Netherlands)

    Kartal, B.; De Almeida, N.M.; Maalcke, W.J.; Op den Camp, H.J.M.; Jetten, M.S.M.; Keltjens, J.T.

    2013-01-01

    Anaerobic ammonium-oxidizing (anammox) bacteria primarily grow by the oxidation of ammonium coupled to nitrite reduction, using CO2 as the sole carbon source. Although they were neglected for a long time, anammox bacteria are encountered in an enormous species (micro)diversity in virtually any anoxi

  4. Hydrothermal oxidation of organic wastes using reclaimed ammonium nitrate

    Energy Technology Data Exchange (ETDEWEB)

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

    1996-04-01

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

  5. 21 CFR 172.165 - Quaternary ammonium chloride combination.

    Science.gov (United States)

    2010-04-01

    ... HUMAN CONSUMPTION Food Preservatives § 172.165 Quaternary ammonium chloride combination. The food... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Quaternary ammonium chloride combination. 172.165 Section 172.165 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN...

  6. Seasonal patterns of ammonium regeneration from size-fractionated microheterotrophs

    Science.gov (United States)

    Maguer, Jean-François; L'Helguen, Stéphane; Madec, Christian; Le Corre, Pierre

    1999-11-01

    Ammonium regeneration by size-fractionated plankton was measured for 1 year at a coastal station in the shallow well-mixed waters of the western English Channel. Rates of ammonium regeneration in the Journal of Plankton Research, 18, 355-370). Total ammonium regenerated in a year by the microheterotrophs was 15 g N m -2, equivalent to about 60% of the total nitrogen uptake. Microplankton (200-15 μm) accounted for about 50% of the regeneration measured between early spring and late summer. Percent contribution of nanoplankton to total ammonium regeneration varied considerably between the seasons, from very high (83-88%) levels in winter to very low (2-13%) levels in summer. Contribution by picoplankton (nano- and picoplankton fractions, appears to be different from that in deep well-mixed waters. Here, the relative contribution of ciliates and bacteria to ammonium regeneration shows little variation with an increase in macrozooplankton biomass.

  7. Colorimetric and atomic absorption spectrometric determination of mucolytic drug ambroxol through ion-pair formation with iron and thiocyanate.

    Science.gov (United States)

    Levent, Abdulkadir; Sentürk, Zühre

    2010-09-01

    Colorimetric and atomic absorption spectrometric methods have been developed for the determination of mucolytic drug Ambroxol. These procedures depend upon the reaction of iron(III) metal ion with the drug in the presence of thiocyanate ion to form stable ion-pair complex which extractable chloroform. The red-coloured complex was determined either colorimetrically at 510 nm or by indirect atomic absorption spectrometry (AAS) via the determination of the iron content in the formed complex. The optimum experimental conditions for pH, concentrations of Fe(3+) and SCN(-), shaking time, phase ratio, and the number of extractions were determined. Under the proposed conditions, linearity was obeyed in the concentration ranges 4.1x10(-6) - 5.7x10(-5) M (1.7-23.6 µg mL(-1)) using both methods, with detection limits of 4.6x10(-7) M (0.19 µg mL(-1)) for colorimetry and 1.1x10(-6) M (0.46 µg mL(-1)) for AAS. The proposed methods were applied for the determination of Ambroxol in tablet dosage forms. The results obtained were statistically analyzed and compared with those obtained by applying the high-performance liquid chromatographic method with diode-array detection.

  8. Spectrophotometric determination of ampicillin, dicluxacillin, flucloxacillin and amoxicillin antibiotic drugs: ion-pair formation with molybdenum and thiocyanate.

    Science.gov (United States)

    Mohamed, G G

    2001-02-01

    A sensitive spectrophotometric method is developed for the determination of some antibiotic drugs such as ampicillin (amp), dicluxacillin (dicl), flucloxacillin (fluc) and amoxicillin (amox). The method involves the formation of ion-pairs between these drugs under investigation and inorganic complex of Mo (V) thiocyanate followed by its extraction with methylene chloride. The optimum conditions for the ion-pairs formation are established. The method permits the determination of amp, dicl, fluc and amox over a concentration range of 1.5-77.5, 3-75, 1.5-79 and 7.5-75 microg ml(-1) respectively. The sensitivity (S) is found to be 0.017, 0.061, 0.014 and 0.073 microg cm(-2) for amp, dicl, fluc and amox, respectively. The method is simple, rapid, reproducible and accurate within +/- 1%. The method is applicable for the assay of the four drugs under investigation in different dosage forms and the results are in good agreement with those obtained by the official method.

  9. Assembly and Crystal Structure of a Novel 1-D Coordination Polymer of Copper(Ⅱ) with Thiocyanate and 4-Cyanopyridine

    Institute of Scientific and Technical Information of China (English)

    LI,Xiu-Yan(李秀艳); WANG,Ping(王平); WANG,Zhe-Ming(王哲明); YAN,Chun-Hua(严纯华); ZHANG,Li-Dan(张丽丹); GUO,Hong-You(郭洪猷)

    2002-01-01

    A novel one-dimensional coordination polymer, Catena-poly [bis(4-cyano-pyridyl) copper(Ⅱ)-di-thiocyanate ], 1∞[CuⅡ-(cypy)2(μN,s-SCN)2] (cypy=4-cyano-pyridyl), was synthe sized in a solution reaction of Cu(NO3)2@3H2O, 4-cyano-pyri dine and KSCN in mole ratio of 1:2:2 at room temperature.Its crystal structure was determined by single-crystal X-ray diffraction. The crystal belongs to monoclinic crystal system,space group P21/c with cell parameters a = 1.0719(2), b =1.8441(4), c =0.9144(2) nm, β= 110.49(3)° and Z=4. Afull-matrix least-squares refinement gave Ri = 0. 0393 and wR2 = 0. 0916 for 1554 reflections having Ⅰ> 2σ (Ⅰ). The crystal is thermally stable up to approximately 170 ℃.

  10. Novel bimetallic thiocyanate-bridged Cu(II)-Hg(II) compounds—synthesis, X-Ray studies and magnetic properties

    Science.gov (United States)

    Machura, B.; Świtlicka, A.; Zwoliński, P.; Mroziński, J.; Kalińska, B.; Kruszynski, R.

    2013-01-01

    Seven novel heterobimetallic Cu/Hg polymers based on thiocyanate bridges have been synthesised and characterised by means of IR, EPR, magnetic measurements and single crystal X-Ray. Three of them, [Cu(pzH)4Hg(SCN)4]n (1) [Cu(indH)4Hg(SCN)4]n (2) and [Cu(ampy)2Hg(SCN)4]n (3), have one-dimensional coordination structure. Two compounds [Cu(pzH)2Hg(SCN)4]n (4) and [Cu(abzimH)Hg(SCN)4]n (5) form two-dimensional nets, whereas the complexes [Cu(pyCN)2Hg(SCN)4]n (6) and [Cu(pyCH(OH)(OMe))2Hg(SCN)4]n (7) are three-dimensional coordination polymers. The chains of 1 are connected by the intermolecular N-H•••N hydrogen bonds to the three dimensional net. In 2 the N-H•••S hydrogen bonds link the polymeric chains to the two dimensional layer extending along crystallographic (0 0 1) plane. The polymeric chains of compound 3 are joined by the intermolecular N-H•••N and N-H•••S hydrogen bonds to the three dimensional net. The polymeric layers of 4 are connected by the intermolecular N-H•••N hydrogen bonds to the three dimensional net.

  11. Urea as a long-term stable alternative to guanidium thiocyanate additive in dye-sensitized solar cell

    Science.gov (United States)

    Kim, Mi-Jeong; Park, Nam-Gyu

    2012-09-01

    Photovoltaic performance of 0.05 M urea-contained redox electrolyte is compared to that of 0.05 M guanidinium thiocyanate (GSCN)-contained one in dye-sensitized solar cell. No significant difference in the initial photovoltaic performance is observed, which means that the role of urea additive is similar to that of GSCN. Initial solar-to-electrical conversion efficiency of the device containing GSCN shows 7% that is diminished to 5.8% after 40 days, whereas the device containing urea exhibits stable photovoltaic performance showing that initial efficiency of 7.2% is almost remained unchanged after 40 days (7.1%). The lowered efficiency of the GSCN-contained device is mainly due to the decreased photocurrent density, which is ascribed to the formation of needle-shaped crystals on TiO2 layer. Infrared spectroscopic study confirms that the crystals are dye analogue, which is indicative of dye desorption in the presence of GSCN. On the other hand, no crystals are formed in the urea-contained electrolyte, which implies that dye desorption is negligible. Urea additive is thus found to be less reactive in dye desorption than GSCN, leading to long-term stability.

  12. The crystal structure of the thiocyanate-forming protein from Thlaspi arvense, a kelch protein involved in glucosinolate breakdown.

    Science.gov (United States)

    Gumz, Frauke; Krausze, Joern; Eisenschmidt, Daniela; Backenköhler, Anita; Barleben, Leif; Brandt, Wolfgang; Wittstock, Ute

    2015-09-01

    Kelch repeat-containing proteins are involved in diverse cellular processes, but only a small subset of plant kelch proteins has been functionally characterized. Thiocyanate-forming protein (TFP) from field-penny cress, Thlaspi arvense (Brassicaceae), is a representative of specifier proteins, a group of kelch proteins involved in plant specialized metabolism. As components of the glucosinolate-myrosinase system of the Brassicaceae, specifier proteins determine the profile of bioactive products formed when plant tissue is disrupted and glucosinolates are hydrolyzed by myrosinases. Here, we describe the crystal structure of TaTFP at a resolution of 1.4 Å. TaTFP crystallized as homodimer. Each monomer forms a six-blade β-propeller with a wide "top" and a narrower "bottom" opening with distinct strand-connecting loops protruding far beyond the lower propeller surface. Molecular modeling and mutational analysis identified residues for glucosinolate aglucone and Fe(2+) cofactor binding within these loops. As the first experimentally determined structure of a plant kelch protein, the crystal structure of TaTFP not only enables more detailed mechanistic studies on glucosinolate breakdown product formation, but also provides a new basis for research on the diverse roles and mechanisms of other kelch proteins in plants. PMID:26260516

  13. Thiocyanate-free asymmetric ruthenium(II) dye sensitizers containing azole chromophores with near-IR light-harvesting capacity

    Science.gov (United States)

    Wu, Guohua; Kaneko, Ryuji; Islam, Ashraful; Zhang, Yaohong; Sugawa, Kosuke; Han, Liyuan; Shen, Qing; Bedja, Idriss; Gupta, Ravindra Kumar; Otsuki, Joe

    2016-11-01

    A new series of thiocyanate-free bis-tridentate Ru(II) complexes containing azole ligands as well as an organometallic Ru-C bond are synthesized, characterized, and evaluated in dye-sensitized solar cells (DSSCs). CF3-substituted pyrazolyl, CF3-substituted triazolyl, and tetrazolyl derivatives are employed as ligands in the three neutral complexes PYZ, TRZ, and TEZ dyes, respectively. Despite their different structures, all the three complexes exhibit similar absorption features and panchromatic absorption covering the visible and near-IR regions. By switching from a pyrazolyl via triazolyl to tetrazolyl moiety in the ligand, the photocurrent value, open-circuit voltage, and overall efficiency are increased accordingly under the same conditions. Among them, photon-to-current conversion efficiency (ƞ) of TEZ dye reaches the maximum of 6.44% with a short-circuit photocurrent density (Jsc) of 17.8 mA cm-2, an open-circuit photovoltage (Voc) of 0.54 V and fill factor (FF) of 0.67 under illumination of an AM1.5G solar simulator. TEZ dye shows a good long term light soaking stability and maintains up to more than 90% of the initial power conversion efficiency after 1000 h.

  14. Copper(I) thiocyanate (CuSCN) as a hole-transport material for large-area opto/electronics

    International Nuclear Information System (INIS)

    Recent advances in large-area optoelectronics research have demonstrated the tremendous potential of copper(I) thiocyanate (CuSCN) as a universal hole-transport interlayer material for numerous applications, including transparent thin-film transistors, high-efficiency organic and hybrid organic-inorganic photovoltaic cells, and organic light-emitting diodes. CuSCN combines intrinsic hole-transport (p-type) characteristics with a large bandgap (>3.5 eV) which facilitates optical transparency across the visible to near infrared part of the electromagnetic spectrum. Furthermore, CuSCN is readily available from commercial sources while it is inexpensive and can be processed at low-temperatures using solution-based techniques. This unique combination of desirable characteristics makes CuSCN a promising material for application in emerging large-area optoelectronics. In this review article, we outline some important properties of CuSCN and examine its use in the fabrication of potentially low-cost optoelectronic devices. The merits of using CuSCN in numerous emerging applications as an alternative to conventional hole-transport materials are also discussed. (paper)

  15. Polyphasic bacterial community analysis of an aerobic activated sludge removing phenols and thiocyanate from coke plant effluent

    Energy Technology Data Exchange (ETDEWEB)

    Felfoldi, T.; Szekely, A.J.; Goral, R.; Barkacs, K.; Scheirich, G.; Andras, J.; Racz, A.; Marialigeti, K. [Eotvos Lorand University, Budapest (Hungary). Dept. of Microbiology

    2010-05-15

    Biological purification processes are effective tools in the treatment of hazardous wastes such as toxic compounds produced in coal coking. In this study, the microbial community of a lab-scale activated sludge system treating coking effluent was assessed by cultivation-based (strain isolation and identification, biodegradation tests) and culture-independent techniques (sequence-aided T-RFLP, taxon-specific PCR). The results of the applied polyphasic approach showed a simple microbial community dominated by easily culturable heterotrophic bacteria. Comamonas badia was identified as the key microbe of the system, since it was the predominant member of the bacterial community, and its phenol degradation capacity was also proved. Metabolism of phenol, even at elevated concentrations (up to 1500 mg/L), was also presented for many other dominant (Pseudomonas, Rhodanobacter, Oligella) and minor (Alcaligenes, Castellaniella, Microbacterium) groups, while some activated sludge bacteria (Sphingomonas, Rhodopseudomonas) did not tolerate it even in lower concentrations (250 mg/L). In some cases, closely related strains showed different tolerance and degradation properties. Members of the genus Thiobacillus were detected in the activated sludge, and were supposedly responsible for the intensive thiocyanate biodegradation observed in the system. Additionally, some identified bacteria (e.g. C. badia and the Ottowia-related strains) might also have had a significant impact on the structure of the activated sludge due to their floc-forming abilities.

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

    Science.gov (United States)

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

    1999-01-01

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

  17. 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.

  18. 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

  19. Correlation of anaerobic ammonium oxidation and denitrification

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The feasibility of the nitrous organic wastewater treated was studied in seven anaerobic sequencing batch reactors(ASBRs)(0 #-6 #) which had been run under stable anaerobic ammonium oxidation (Anammox). By means of monitoring and data analysis of COD, NH4+-N, NO2--N, NO3--N and pH, and of microbial test, the results revealed that the optimal Anammox performance was achieved from 2# reactor in which COD/NH4+-N was 1.65, Anammox bacteria and denitrification bacteria could coexist, and Anammox reaction and denitrification reaction could occur simultaneously in the reactors. The ratio of NH4+-N consumed: NO2--N consumed: NO3--N produced was 1:1.38:0.19 in 0# reactor which was not added glucose in the wastewater. When different ratio of COD and NH4+-N was fed for the reactors, the ratio of NO2--N consumed: NH4+-N consumed was in the range of 1.51-2.29 and the ratio of NO3-N produced: NH4+-N consumed in the range of 0-0.05.

  20. Influence of the Different Level Ammonium on NRA and GSA in Sugar Beet(Vulgaris L.)

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Ammonium nitrogen inhibited NR activity in sugar beet,NR activity was lower in endogenous substrate after ammonium nitrogen was used,and the correlation between NR activity and ammonium nitrogen levels was negative.But NR activity raised with the ammonium nitrogen levels raising in exogenous.Ammonium nitrogen prompted GS activity:the correlation between GS activity and ammonium nitrogen was positive,GS activity raised with ammonium nitrogen levels raising,GS activity of roots and leaves had same change trend in sugar beet in the whole growth duration after ammonium nitrogen was used,but GS activity in roots was higher than that in leaves.

  1. Effect of Ammonium Nitrate on Nanoparticle Size Reduction

    Directory of Open Access Journals (Sweden)

    Kalyana C. Pingali

    2008-01-01

    Full Text Available Ammonium nitrate was added to the spraying solution as a foaming agent to reduce the particle size of nanoparticles synthesized in the spray-pyrolysis process. Ammonium nitrate was effective in breaking the aerosol droplet size and generating nanoparticles that were of approximately one order-of-magnitude (from 200 to 20 nm smaller diameter than those created in the absence of ammonium nitrate in the feed solution. This technique makes it possible to control the particle diameter of metallic nanoparticles below 20 nm.

  2. {sup 14}N NQR and relaxation in ammonium nitrate

    Energy Technology Data Exchange (ETDEWEB)

    Stephenson, David, E-mail: david.stephenson@sta.uwi.edu [University of the West Indies, Chemistry Department (Trinidad and Tobago)

    2015-04-15

    The complete {sup 14}N nuclear quadrupole resonance (NQR) spectrum of ammonium nitrate is presented recorded using two double resonance techniques – double contact cross relaxation and zero field NQR. The spectra gave the quadrupole coupling constant (Qcc) and asymmetry parameter (η) values for the nitro of 611 kHz, 0.229 and that for the ammonium nitrogen of 242 kHz, 0.835. The three relaxation transition probabilities have been determined for both the nitro and ammonium nitrogen atoms. The bi-exponential relaxation times (T {sub 1}) were measured at 295 K. The values for nitro are 16.9 s and 10.5 s and that of the ammonium are 23.0 s and 16.4 s.

  3. Ammonium removal by modified zeolite from municipal wastewater

    Institute of Scientific and Technical Information of China (English)

    ZHAO Ya-ping; GAO Ting-yao; JIANG Shang-ying; CAO Da-wen

    2004-01-01

    Ammonium removal by modified zeolite, H-form and Na-form zeolite, were examined by batch-type methods. The adsorption of ammonium on modified zeolite was exothermic process. The saturation adsorption capacity of ammonium on H-form and Na-form zeolite were 21.23 and 41.15 mg/g, respectively. After ten times adsorption- desorption-readsorption cycles the standard deviations of H-form and Na-form zeolite were 6.34% and 6.59%. The zeolite adsorption process has proved cost effective and practical in reducing ammonium by H-form and Na-form zeolite in municipal wastewater from concentration 27.68 mg/L to 2.80 mg/L and 5.91 mg/L.

  4. Fixed Ammonium Content and Maximum Capacity of Ammonium Fixation in Major Types of Tillage Soils in Hunan Province, China

    Institute of Scientific and Technical Information of China (English)

    ZHANG Yang-zhu; HUANG Shun-hong; WAN Da-juan; HUANG Yun-xiang; ZHOU Wei-jun; ZOU Ying-bin

    2007-01-01

    In order to understand the status of fixed ammonium, fixed ammonium content, maximum capacity of ammonium fixation, and their influencing factors in major types of tillage soils of Hunan Province, China, were studied with sampling on fields, and laboratory incubation and determination. The main results are summarized as follows: (1) Content of fixed ammonium in the tested soils varies greatly with soil use pattern and the nature of parent material. For the paddy soils, it ranges from 135.4 ± 57.4 to 412.8±32.4 mg kg-1, with 304.7±96.7 mg kg-1 in average; while it ranges from 59.4 to 435.7 mg kg-1, with 230.1 ± 89.2 mg kg1 in average for the upland soils. The soils developed from limnic material and slate had higher fixed ammonium content than the soils developed from granite. The percentage of fixed ammonium to total N in the upland soils is always higher than that in the paddy soils. It ranges from 6.1 ± 3.6% to 16.6 ±4.6%, with 14.0% ± 5.1% in average for the paddy soils and it amounted to 5.8 ±2.0% to 40.1 ± 17.8%, with 23.5 ± 14.2% in average for upland soils. (2) The maximum capacity of ammonium fixation has the same trend with the fixed ammonium content in the tested soils. For all the tested soils, the percentage of recently fixed ammonium to maximum capacity of ammonium fixation is always bellow 20% and it may be due to the fact that the soils have high fertility and high saturation of ammonium-fixing site. (3) The clay content and clay composition in the tested soils are the two important factors influe ncing their fixed ammonium content and maximum capacity of ammonium fixation. The results showed that hydrous mica is the main 2:1 type clay mineral in <0.02 mm clay of the paddy soils, and its content in 0.02-0.002 mm clay is much higher than that in < 0.002 mm clay of the soils. The statistical analysis showed that both the fixed ammonium content and the maximum capacity of ammonium fixation of the paddy soils were positively correlated with

  5. Synthesis, characterization, and bioactivity of rosin quaternary ammonium salt derivatives

    Directory of Open Access Journals (Sweden)

    Tao Liang

    2013-02-01

    Full Text Available Two series of rosin quaternary ammonium salts (QAS were synthesized using the same path. The structure of the target products was characterized by HPLC, MS, IR, and 1HNMR, and the bioactivity was determined by filter paper method using Trametes versicolor (white-rot fungus and Gloeophyllum trabeum (brown-rot fungus, which are two kinds of general wood decay fungi in nature. The results showed that all compounds tested had a satisfactory anti-fungal effect at the molarity of 0.025 mmol/mL. Hereinto, acrylpimaric Gemini QAS had better bioactivity than dehydrogenated or tetrahydrogenated rosin QAS against Trametes versicolor. To this fungus, quaternary ammonium groups, which wraps up the membrane of microorganism and disrupts the balance in cell membrane, plays the leading role for its bioactivity. To Gloeophyllum trabeum, the inhibition activity of acrylpimaric QAS and dehydrogenated rosin QAS are almost at the same level and larger than tetrahydrogenated rosin QAS, so we conclude that both quaternary ammonium group and aromatic group play important roles. Compared with dodecyl dimethyl benzyl ammonium chloride (1227, which is a commercially available quaternary ammonium salt type fungicide, acrylpimaric acid quaternary ammonium salts have approximate bioactivity against Gloeophyllum trabeum. In conclusion, rosin derivatives with functional groups would do well in wood preservative applications.

  6. 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.

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

    Science.gov (United States)

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

    2015-01-01

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

  8. New family of thiocyanate-bridged Re(IV)-SCN-M(II) (M = Ni, Co, Fe, and Mn) heterobimetallic compounds: synthesis, crystal structure, and magnetic properties.

    Science.gov (United States)

    González, Ricardo; Acosta, Alvaro; Chiozzone, Raúl; Kremer, Carlos; Armentano, Donatella; De Munno, Giovanni; Julve, Miguel; Lloret, Francesc; Faus, Juan

    2012-05-21

    The heterobimetallic complexes of formula [(Me(2)phen)(2)M(μ-NCS)Re(NCS)(5)]·CH(3)CN [Me(2)phen = 2,9-dimethyl-1,10-phenanthroline and M = Ni (1), Co (2), Fe (3), and Mn (4)] have been prepared, and their crystal structures have been determined by X-ray diffraction on single crystals. Compounds 1-4 crystallize in the monoclinic C2/c space group, and their structure consists of neutral [(Me(2)phen)(2)M(μ-NCS)Re(NCS)(5)] heterodinuclear units with a Re-SCN-M bridge. Each Re(IV) ion in this series is six-coordinated with one sulfur and five nitrogen atoms from six thiocyanate groups building a somewhat distorted octahedral environment, whereas the M(II) metal ions are five-coordinated with four nitrogen atoms from two bidentate Me(2)phen molecules and a nitrogen atom from the bridging thiocyanate describing distorted trigonal bipyramidal surroundings. The values of the Re···M separation through the thiocyanate bridge in 1-4 vary in the range 5.903(1)-6.117(3) Å. The magnetic properties of 1-4 as well as those of the parent mononuclear Re(IV) compounds (NBu(4))(2)[Re(NCS)(6)] (A1) (NBu(4)(+) = tetra-n-butylammonium cation) and [Zn(NO(3))(Me(2)phen)(2)](2)[Re(NCS)(5)(SCN)] (A2) were investigated in the temperature range 1.9-300 K. Weak antiferromagnetic interactions between the Re(IV) and M(II) ions across the bridging thiocyanate were found in 1-4 [J = -4.3 (1), -2.4 (2), -1.8 (3), and -1.2 cm(-1) (4), the Hamiltonian being defined as Ĥ = -JŜ(Re)·Ŝ(M)]. The magnetic behavior of A2 is that of a magnetically diluted Re(IV) complex with a large and positive value of the zero-field splitting for the ground level (D(Re) = +37.0 cm(-1)). In the case of A1, although its magnetic behavior is similar to that of A2 in the high-temperature range (D(Re) being +19.0 cm(-1)), it exhibits a weak ferromagnetism below 3.0 K with a canting angle of 1.3°. PMID:22574893

  9. Thermal Thiocyanate Ligand Substitution Kinetics of the Solar Cell Dye N719 by Acetonitrile, 3-Methoxypropionitrile, and 4-tert-Butylpyridine

    DEFF Research Database (Denmark)

    Nguyen, Thai Hoang; Minh, Ha; Lund, Torben

    2007-01-01

    the same products as occur in the homogenous solutions; however, the reactions are approximately 10 times faster. For the reaction of a colloidal mixture of N719-dyed TiO2 particles in acetonitrile containing 0.5 M 4-TBP, a t1/2(het) of 120 h was calculated at 85°C. The N719-based DSSC cells...... by a factor of 2-10; it thus may be used as an additive to prevent the thermal degradation of thiocyanate-based ruthenium complexes in DSSC solar cells....

  10. New family of thiocyanate-bridged Re(IV)-SCN-M(II) (M = Ni, Co, Fe, and Mn) heterobimetallic compounds: synthesis, crystal structure, and magnetic properties.

    Science.gov (United States)

    González, Ricardo; Acosta, Alvaro; Chiozzone, Raúl; Kremer, Carlos; Armentano, Donatella; De Munno, Giovanni; Julve, Miguel; Lloret, Francesc; Faus, Juan

    2012-05-21

    The heterobimetallic complexes of formula [(Me(2)phen)(2)M(μ-NCS)Re(NCS)(5)]·CH(3)CN [Me(2)phen = 2,9-dimethyl-1,10-phenanthroline and M = Ni (1), Co (2), Fe (3), and Mn (4)] have been prepared, and their crystal structures have been determined by X-ray diffraction on single crystals. Compounds 1-4 crystallize in the monoclinic C2/c space group, and their structure consists of neutral [(Me(2)phen)(2)M(μ-NCS)Re(NCS)(5)] heterodinuclear units with a Re-SCN-M bridge. Each Re(IV) ion in this series is six-coordinated with one sulfur and five nitrogen atoms from six thiocyanate groups building a somewhat distorted octahedral environment, whereas the M(II) metal ions are five-coordinated with four nitrogen atoms from two bidentate Me(2)phen molecules and a nitrogen atom from the bridging thiocyanate describing distorted trigonal bipyramidal surroundings. The values of the Re···M separation through the thiocyanate bridge in 1-4 vary in the range 5.903(1)-6.117(3) Å. The magnetic properties of 1-4 as well as those of the parent mononuclear Re(IV) compounds (NBu(4))(2)[Re(NCS)(6)] (A1) (NBu(4)(+) = tetra-n-butylammonium cation) and [Zn(NO(3))(Me(2)phen)(2)](2)[Re(NCS)(5)(SCN)] (A2) were investigated in the temperature range 1.9-300 K. Weak antiferromagnetic interactions between the Re(IV) and M(II) ions across the bridging thiocyanate were found in 1-4 [J = -4.3 (1), -2.4 (2), -1.8 (3), and -1.2 cm(-1) (4), the Hamiltonian being defined as Ĥ = -JŜ(Re)·Ŝ(M)]. The magnetic behavior of A2 is that of a magnetically diluted Re(IV) complex with a large and positive value of the zero-field splitting for the ground level (D(Re) = +37.0 cm(-1)). In the case of A1, although its magnetic behavior is similar to that of A2 in the high-temperature range (D(Re) being +19.0 cm(-1)), it exhibits a weak ferromagnetism below 3.0 K with a canting angle of 1.3°.

  11. Hole-transporting transistors and circuits based on the transparent inorganic semiconductor copper(I) thiocyanate (CuSCN) processed from solution at room temperature

    KAUST Repository

    Pattanasattayavong, Pichaya

    2012-12-27

    The wide bandgap and highly transparent inorganic compound copper(I) thiocyanate (CuSCN) is used for the first time to fabricate p-type thin-film transistors processed from solution at room temperature. By combining CuSCN with the high-k relaxor ferroelectric polymeric dielectric P(VDF-TrFE-CFE), we demonstrate low-voltage transistors with hole mobilities on the order of 0.1 cm2 V-1 s-1. By integrating two CuSCN transistors, unipolar logic NOT gates are also demonstrated. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Alkylphenol derivatives of the polymer of thiocyanic acid and 5-amino-1,2,4-dithiazole-3-thione as an effective additives to fuels and lubricants

    OpenAIRE

    Vasylkevych, Oleksandr; Kofanova, Olena; Tkachuk, Kostyantyn; Kofanov, Oleksii

    2016-01-01

    For ensuring the operation of the mechanisms at high temperatures and pressures, it is necessary to use both stable base oils and effective additives in the composition of the lubricants. In the research, antioxidative and anticorrosive properties were identified in the oils of the condensation products of the alkylphenols with paraformaldehyde and thiocyanic acid polymer. The condensation products of the 5­amino­1,2,4­dithiazole­3­thione (Xanthane Hydride) with the 2,6­di­tert­Butylphenol an...

  13. New synthetic method and properties of ammonium dinitramide; Ammonium dinitramide no shingoseiho to sono butsuri kagakuteki tokusei

    Energy Technology Data Exchange (ETDEWEB)

    Hatano, H.; Onda, T.; Shiino, K. [Hosoya Kako Co. Ltd., Tokyo (Japan). Technology and Development Center; Miyazaki, S.; Matsuura, S. [Nissan Motor Co. Ltd., Saitama (Japan). Research and Development center

    1996-08-31

    Though, ammonium nitrate (AN) has been thought as solid propellant oxidizer, at present, ammonium perchlorate (AP) is mainly used because of the existence of crystal transition point, the improvement of propellant performance on AN and so forth. Ammonium dinitramide (ADN) can be used as an excellent oxidizer for high performance solid propellants, because it has much available oxygen. Furthermore, this propellant is smokeless, since ADN has no halogen resulting in generation of smoke on burning. ADN can be obtained by a new synthetic method which uses urea as starting substance and acquires nitrourea as intermediate product. According to this method, the yield is about 15% based on the amount of nitrourea. The hygroscopicity of this ADN is slightly higher than that of ammonium nitrate. Therefore, it is recommended to handle this substance at 50% of relative humidity or below. 13 refs., 7 figs., 4 tabs.

  14. Methods to Stabilize and Destabilize Ammonium Borohydride

    Energy Technology Data Exchange (ETDEWEB)

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

    2013-01-21

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

  15. 76 FR 49449 - Continuation of Antidumping Duty Order on Solid Fertilizer Grade Ammonium Nitrate From the...

    Science.gov (United States)

    2011-08-10

    ... International Trade Administration Continuation of Antidumping Duty Order on Solid Fertilizer Grade Ammonium... duty investigation on solid fertilizer grade ammonium nitrate (``ammonium nitrate'') from the Russian... Initiation of Five-Year (``Sunset'') Review, 76 FR 11202 (March 1, 2011) and Ammonium Nitrate from...

  16. Effects of Temperature and Drying and Wetting Alternation on Ammonium Fixation in Manured Loessial Soil

    Institute of Scientific and Technical Information of China (English)

    FANXIAOLIN; LILING; 等

    1996-01-01

    Effects of temperature and drying and wetting alternation (DWA) on ammonium fixation in manured loessial soil were studied by means of Batch Equilibrium with varying concentration solutions of ammonium chloride.ammonium fixation time,and soil clay contents.The purpose of the research was to find out the pattern of ammonium fixation affected by the varying factors.The results showed a remarkable variation in ammonium fixation.Fixed ammonium increased with temperature and treatments of DWA.The ammonium fixation in manured loessial soil was characterized by the effect of temperature and DWA.

  17. 结晶紫-硫氰酸铵体系浮选分离钌(Ⅲ)%Separation of Ruthenium(Ⅲ) by Floatation as Its Ternary Association Complex with Crystal Violet and Ammonium Thiocyanate

    Institute of Scientific and Technical Information of China (English)

    马万山; 曹书勤; 孙俊永

    2007-01-01

    在水溶液中Ru(Ⅲ)与硫氰酸铵、结晶紫形成不溶于水的三元缔合物,在少量氯化钠存在下,此三元缔合物沉淀浮于盐水相上层形成界面清晰的液-固两相.当溶液中氯化钠、硫氰酸铵、结晶紫的质量浓度分别为50 g·L-1、0.04 mol·L-1、2.5×10-4mol·L-1,pH 4.0时,Ru(Ⅲ)被定量浮选.Rh(Ⅲ)、Mn(Ⅱ)、Al(Ⅲ)、Ni(Ⅱ)、Cr(Ⅲ)、Cd(Ⅱ)、V(Ⅴ)、Fe(Ⅱ)离子在该体系中不被浮选,实现了Ru(Ⅲ)与这些离子的定量分离,对合成水样和纯镍中钌进行定量浮选分离测定.

  18. 氯化钠-硫氰酸铵-结晶紫体系浮选分离锌(Ⅱ)%Separation of Zinc by Sodium Chloride-Ammonium Thiocyanate-Crystal Violet Floatation System

    Institute of Scientific and Technical Information of China (English)

    李全民; 白海鑫; 吕文英

    2002-01-01

    研究了氯化钠-硫氰酸铵-结晶紫体系浮选分离锌(Ⅱ)的行为. 研究表明,在水溶液中,Zn(Ⅱ)与NH4SCN、结晶紫(CV)生成三元离子缔合物沉淀[Zn(SCN)2-4]*(CV+)2. 在少量NaCl存在下,该沉淀能很好地浮于水相表面并和水完全分离. 在水相pH值为1~4时,通过浮选可使Zn(Ⅱ)与Fe(Ⅲ)、Al(Ⅲ)、Ni(Ⅱ)、Mn(Ⅱ)、Cd(Ⅱ)离子的完全分离.

  19. 激光法测定硫氰酸铵结晶介稳区宽度%Measurement of Crystallization Metastable Zone Width of Ammonium Thiocyanate with Laser Scattering Method

    Institute of Scientific and Technical Information of China (English)

    党乐平; 颜雯雯; 卫宏远

    2009-01-01

    用激光法测定了不同温度下硫氰酸铵在水、甲醇、乙醇和w(乙醇)=95%4种溶剂体系中的溶解与超溶解特性,得到硫氰酸铵在不同温度下不同溶剂中的介稳区宽度.结果表明,硫氰酸铵在4种溶剂体系中介稳区宽度均随温度的升高而降低.在相同温度下,硫氰酸铵在水、甲醇、乙醇和w(乙醇)=95%中介稳区宽度顺序为:水<甲醇

  20. Thiocyanate cadmium(II) complexes of 2,4,6-tri(2-pyridyl)-1,3,5-triazine – Synthesis, structure and luminescence properties

    Energy Technology Data Exchange (ETDEWEB)

    Nawrot, I. [Department of Crystallography, Institute of Chemistry, University of Silesia, ul. Szkolna 9, 40-006 Katowice (Poland); Machura, B., E-mail: basia@ich.us.edu.pl [Department of Crystallography, Institute of Chemistry, University of Silesia, ul. Szkolna 9, 40-006 Katowice (Poland); Kruszynski, R., E-mail: rafal.kruszynski@p.lodz.pl [Department of X-ray Crystallography and Crystal Chemistry, Institute of General and Ecological Chemistry, Lodz University of Technology, ul. Żeromskiego 116, 90-924 Łódź (Poland)

    2014-12-15

    Two new thiocyanate cadmium(II) complexes of 2,4,6-tri(2-pyridyl)-1,3,5-triazine were synthesized and characterized. The resulted complexes [Cd(SCN)(NO{sub 3})(tptz)(H{sub 2}O)] (1) and [Cd(SCN){sub 2}(tptz)(MeOH)] (2) were studied by IR, UV–vis spectroscopy and single crystal X-ray analysis. The luminescent properties of 1 and 2 were studied in solution and solid state and compared with the free ligand. To get detailed insight into the electronic structure and spectroscopic properties of [Cd(SCN)(NO{sub 3})(tptz)(H{sub 2}O)] and [Cd(SCN){sub 2}(tptz)(MeOH)], the density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations were performed. - Highlights: • Two novel thiocyanate cadmium(II) compounds of 2,4,6-tri(2-pyridyl)-1,3,5-triazine were synthesized. • The compounds were identified by IR, UV–vis spectroscopy and X-ray analysis. • The fluorescence properties of the complexes were examined and compared with the free ligand. • The electronic spectra were investigated at the TD-DFT level employing B3LYP/LANL2DZ.

  1. Spectrophotometric determination of some anti-tussive and anti-spasmodic drugs through ion-pair complex formation with thiocyanate and cobalt(II) or molybdenum(V)

    Science.gov (United States)

    El-Shiekh, Ragaa; Zahran, Faten; El-Fetouh Gouda, Ayman Abou

    2007-04-01

    Two rapid, simple and sensitive extractive specrophotometric methods has been developed for the determination of anti-tussive drugs, e.g., dextromethorphan hydrobromide (DEX) and pipazethate hydrochloride (PiCl) and anti-spasmodic drugs, e.g., drotaverine hydrochloride (DvCl) and trimebutine maleate (TM) in bulk and in their pharmaceutical formulations. The proposed methods depend upon the reaction of cobalt(II)-thiocyanate (method A) and molybdenum(V)-thiocyanate ions (method B) with the cited drugs to form stable ion-pair complexes which extractable with an n-butnol-dichloromethane solvent mixture (3.5:6.5) and methylene chloride for methods A and B, respectively. The blue and orange red color complexes are determined either colorimetrically at λmax 625 nm (using method A) and 467 or 470 nm for (DEX and PiCl) or (DvCl and TM), respectively (using method B). The concentration range is 20-400 and 2.5-50 μg mL -1 for methods A and B, respectively. The proposed method was successfully applied for the determination of the studied drugs in pure and in pharmaceutical formulations applying the standard additions technique and the results obtained in good agreement well with those obtained by the official method.

  2. Thiocyanate cadmium(II) complexes of 2,4,6-tri(2-pyridyl)-1,3,5-triazine – Synthesis, structure and luminescence properties

    International Nuclear Information System (INIS)

    Two new thiocyanate cadmium(II) complexes of 2,4,6-tri(2-pyridyl)-1,3,5-triazine were synthesized and characterized. The resulted complexes [Cd(SCN)(NO3)(tptz)(H2O)] (1) and [Cd(SCN)2(tptz)(MeOH)] (2) were studied by IR, UV–vis spectroscopy and single crystal X-ray analysis. The luminescent properties of 1 and 2 were studied in solution and solid state and compared with the free ligand. To get detailed insight into the electronic structure and spectroscopic properties of [Cd(SCN)(NO3)(tptz)(H2O)] and [Cd(SCN)2(tptz)(MeOH)], the density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations were performed. - Highlights: • Two novel thiocyanate cadmium(II) compounds of 2,4,6-tri(2-pyridyl)-1,3,5-triazine were synthesized. • The compounds were identified by IR, UV–vis spectroscopy and X-ray analysis. • The fluorescence properties of the complexes were examined and compared with the free ligand. • The electronic spectra were investigated at the TD-DFT level employing B3LYP/LANL2DZ

  3. Quaternary ammonium salt derivatives of allylphenols with peripheral analgesic effect

    Directory of Open Access Journals (Sweden)

    A. B de Oliveira

    1991-01-01

    Full Text Available Ammonium salt derivatives of natural allylphenols were synthesized with the purpose of obtaining potential peripheral analgesics. These drugs, by virtue of their physicochemical properties, would not be able to cross the blood brain barrier. Their inability to enter into the central nervous system (CNS should prevent several adverse effects observed with classical opiate analgesics (Ferreira et al., 1984. Eugenol (1 O-methyleugenol (5 and safrole (9 were submitted to nitration, reduction and permethylation, leading to the ammonium salts 4, 8 and 12. Another strategy applied to eugenol (1, consisting in its conversion to a glycidic ether (13, opening the epoxide ring with secondary amines and methylation, led to the ammonium salts 16 and 17. All these ammonium salts showed significant peripheral analgesic action, in modified version of the Randall-Sellito test (Ferreira et al. 1978, at non-lethal doses. The ammonium salt 8 showed an activity comparable to that of methylnalorphinium, the prototype of an ideal peripheral analgesic (Ferreira et al., 1984.

  4. Difficultly Extractable Fixed Ammonium in Some Soils of China

    Institute of Scientific and Technical Information of China (English)

    CHENBIYUN; CHENGLILI; 等

    1999-01-01

    Ninety-three soil samples and 19 sedimentary rock samples collected from 21 provinces of China were analyzed for their contents of fixed ammonium and total N by Kjeldahl-HF method.Results showed that amount of difficultly extractable fixed ammonium(the fixed ammonium that is not determinable by Kjeldahl procedures commonly used for soils) in soils ranged from 0 to 202 mg kg-1,It was generally more than 50 mg kg-1 in soils in Changji and Turpan districts,Xinjiang,accounting for 3.2%-36.8% with an average of 13.9% of the total N.For some Orthents derived from purple shale and purple sandstone in Sichuan and Hunan provinces and Chao soils derived from secondary loess in Henan Province and Ningxia Autonomous Region it was generally around 30 mg kg-1,accounting for 4%-7% of the total soil N,and for most of the rest of soils studied,with the exception of some subsoils,no or trace difficultly extractable fixed ammonium could be detected.It was sugested that the difficultly extractable fixed ammonium was originated from parent rock,and for slightly weathered soils derived from parent materials rich in this form of N the Kjeldahl method might give underestimation of total soil N.

  5. Performance of sulfate-dependent anaerobic ammonium oxidation

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    The performance of sulfate-dependent anaerobic ammonium oxidation was studied.The results showed that both SO42-and NH4+ were chemically stable under anaerobic conditions.They did not react with each other in the absence of biological catalyst(sludge).The anaerobic digested sludge cultivated in an anaerobic reactor for three years took on the ability of oxidizing ammonium with sulfate anaero-bically.The average reduction of sulfate and ammonium was 71.67 mg.L-1 and 56.82 mg.L-1 at high concentrations.The reaction between SO42-and NH4+ was difficult,though feasible,due to its low standard Gibbs free energy change.The experiment demonstrated that high substrate concentrations and low oxidation-reduction potential(ORP) may be favourable for the biological reaction.

  6. Performance of sulfate-dependent anaerobic ammo-nium oxidation

    Institute of Scientific and Technical Information of China (English)

    ZHANG Lei; ZHENG Ping; HE YuHui; JIN RenCun

    2009-01-01

    The performance of sulfate-dependent anaerobic ammonium oxidation was studied. The results showed that both SO42- and NH4+ were chemically stable under anaerobic conditions. They did not react with each other in the absence of biological catalyst (sludge). The anaerobic digested sludge cultivated in an anaerobic reactor for three years took on the ability of oxidizing ammonium with sulfate anaero-bically. The average reduction of sulfate and ammonium was 71.67 mg.L-1 and 56.82 mg.L-1 at high concentrations.The reaction between SO42- and NH4+ was difficult, though feasible, due to its low standard Gibbs free energy change. The experiment demonstrated that high substrate concentrations and low oxidation-reduction potential (ORP) may be favourable for the biological reaction.

  7. 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...... area, and traced the ammonium processing and retention in four subsequent tide cycles. In this paper we present the results for the water-phase components of the marsh system and compare them to a similar experiment conducted in spring/early summer (May). Changes in concentration and isotopic......, but the absolute ammonium transformation rate was 3 times higher in May. While the marsh surface area was crucial for nitrification in May this was less pronounced in September. Denitrification, on the other hand, appeared more important in September compared to May....

  8. The biological activity of quaternary ammonium salts (QASs

    Directory of Open Access Journals (Sweden)

    Ewa Obłąk

    2010-04-01

    Full Text Available Quaternary ammonium salts (QASs, especially those of cationic surfactant character, are applied as antibacterial and antifungal disinfectants. QASs affect lipid-enveloped viruses, including human immunodeficiency virus (HIV and hepatitis B virus (HBV, but not non-enveloped viruses. These compounds are extensively used in domestic (as ingredients of shampoos, hair conditioners, agricultural (as fungicides, pesticides, insecticides, healthcare (as medications, and industrial applications (as biocides, fabric softeners, corrosion inhibitors. The extensive use of quaternary ammonium disinfectants in recent years has led to the development of resistance in microorganisms to these drugs. Thus [i]Staphylococcus[/i] [i]aureus[/i] strains contain the plasmid-carrying genes [i]qacA[/i] and [i]qacB [/i]encoding resistance to quaternary ammonium compounds and acriflavine. The membrane proteins QacA and QacB confer multidrug resistance by exporting the compound by the proton motive force which is generated by the transmembrane electrochemical proton gradient.

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

    International Nuclear Information System (INIS)

    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)

  10. Enrichment culture of marine anaerobic ammonium oxidation (anammox) bacteria

    Institute of Scientific and Technical Information of China (English)

    GUAN Yong-jie

    2016-01-01

    The present study investigates the enrichment of anaerobic ammonium oxidation (anammox) bacteria in the marine environment using sediment samples obtained from the East China Sea and discusses the nitrogen removal efficiency of marine anammox bioreactor. Enrichment of anammox bacteria with simultaneous removal of nitrite and ammonium ions was observed in the Anaerobic Sequencing Batch Reactor under a total nitrogen loading rate of 0.37kg-N m-3day-1. In this study, The nitrogen removal efficiency was up to 80% and the molar-reaction ratio of ammonium, nitrite and nitrate was 1.0:1.22:0.22 which was a little different from a previously reported ratio of 1.0:1.32:0.26 in a freshwater system.

  11. Surface studies on bimetallic thiocyanate ligand based single crystals of MnHg(SCN){sub 4}, CdHg(SCN){sub 4} and ZnCd(SCN){sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Rajesh Kumar, T.; Jeyasekaran, R. [Department of Physics, Loyola College, Chennai 600 034 (India); Ravi Kumar, S.M. [Department of Physics, Govt. Arts College, Thiruvannamalai 606 603 (India); Vimalan, M. [Physics Research Center, S.T. Hindu College, Nagercoil 629 002 (India); Sagayaraj, P., E-mail: psagayaraj@hotmail.com [Department of Physics, Loyola College, Chennai 600 034 (India)

    2010-12-15

    Bimetallic SCN ligand based single crystals of manganese mercury thiocyanate (MMTC), cadmium mercury thiocyanate (CMTC) and zinc cadmium thiocyanate (ZCTC) are grown by slow solvent evaporation technique. The growth mechanism and surface features are investigated by optical microscopic techniques such as scanning electron microscopy (SEM) and atomic force microscopy (AFM). The laser induced surface damage measurements were carried out using a Q-switched Nd:YAG laser at 1064 nm with laser beam of 1.0 Hz and pulse duration 25 ps. The laser damage threshold values of MMTC, CMTC and ZCTC are found to be 15.9, 22.9 and 19.7 GW/cm{sup 2}, respectively. The SEM analysis of MMTC reveals the formation of elongated dendrite growth pattern caused by the fluctuations of Mn and Hg metal ligands when thiocyanate (SCN) bridges them. The etching study indicates the occurrence of different types of etch pit patterns like terraced triangles, pillars, pyramids and rods. The AFM images confirm the formation of three major hillocks with cavities in MMTC. The measured roughness values for CMTC crystal are very much lower than that of MMTC.

  12. Regioselective ring opening of epoxides using NH4SCN/silica sulfuric acid: An efficient approach for the synthesis of β-hydroxy thiocyanate under solvent-free conditions

    Institute of Scientific and Technical Information of China (English)

    Ali R. Kiasat; Maryam Zayadi; Mehdi Fallah Mehrjardi

    2008-01-01

    Silica sulfuric acid was developed as a stable and efficient heterogeneous catalyst in organic synthesis. This solid acid catalyzed the regioselective ring opening of epoxides by thiocyanate anion to give thiocyanohydrins as key intermediates in agricultural and pharmaceutical chemistry in high yields under solvent-free conditions.

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

    Science.gov (United States)

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

    2011-03-01

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

  14. Laboratory studies of ice formation pathways from ammonium sulfate particles

    Directory of Open Access Journals (Sweden)

    M. E. Wise

    2008-08-01

    Full Text Available Cirrus clouds are composed of ice particles and their formation pathways have been studied extensively in the laboratory. The ability of ammonium sulfate particles to act as nuclei for cirrus clouds has been of particular importance because of their ubiquitous presence in the upper troposphere. The results of past laboratory experiments of homogeneous ice nucleation from ammonium sulfate particles show a wide range of freezing conditions. In the present study, a flow tube apparatus equipped with Fourier transform infrared spectroscopy was used to resolve these discrepancies. It was found that when ammonium sulfate particles were preconditioned at 100% relative humidity (RH prior to experimentation, the particles froze at conditions predicted by the homogeneous ice nucleation model developed by Koop et al. (2000. If the particles were not preconditioned at 100% RH, they froze at warmer temperatures and lower ice saturation ratios than predicted by Koop et al. (2000. In order to determine if a population of effloresced particles affected freezing conditions for particles that were not preconditioned at 100% RH, a series of depositional ice nucleation experiments were carried out on dry ammonium sulfate particles. For freezing temperatures between 215 and 231 K, ice nucleated on the particles at ice saturation ratios (Sice between 1 and 1.05. These conditions are much lower than predicted by Koop et al. (2000 and explain the differences in freezing conditions among preconditioning methods. In similar experiments, Abbatt et al. (2006 hypothesized that a small fraction of effloresced ammonium sulfate particles induced ice nucleation at Sice values lower than expected. The current study confirms the Abbatt et al. (2006 hypothesis and, to our knowledge, is the first study to directly observe ice nucleating onto freely flowing dry ammonium sulfate particles at Sice values approaching unity.

  15. Mutagenic activity of quaternary ammonium salt derivatives of carbohydrates

    Science.gov (United States)

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

    2016-01-01

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

  16. Effect of peroxodisulfate on uranium leaching with ammonium bicarbonate

    Directory of Open Access Journals (Sweden)

    Nurbek Nurpeisov

    2013-05-01

    Full Text Available In this study, uranium leaching from ore material using acid solution and bicarbonate in a presence peroxodisulfate ion was examined. For experiments two different tips of leaching methods were used: leaching in static and dynamic conditions. The determination of uranium concentrations in product solutions were analyzed by titrimetric (by ammonia vanadate solution method. The maximum yield of uranium leached with ammonium bicarbonate in a presence of ammonium peroxodisulfate (5 g/L was only 33%, which is half the corresponding value obtained by sulfuric acid (65%.

  17. Tripropyl­ammonium trithio­cyanurate

    OpenAIRE

    Yang, Yunxia

    2010-01-01

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

  18. Tripropyl­ammonium trithio­cyanurate

    Science.gov (United States)

    Yang, Yunxia

    2010-01-01

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

  19. Aerosol isotopic ammonium signatures over the remote Atlantic Ocean

    Science.gov (United States)

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

    2016-05-01

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

  20. Determination of Ammonium Ion in Lake Water by Voltammetry

    Institute of Scientific and Technical Information of China (English)

    Wu Yun-hua; Fei Jun-jie; Dang Xue-ping; Hu Sheng-shui

    2004-01-01

    An electroanalytical method for the determination of armonium ion using a platinized platinum electrode is described. Under optimized analytical conditions, the linear range of the calibration graphs for ammonium ion is 3. 0×10(-5)-5.0×10-3 mol·L-1.The Method has been applide to the determination of ammonium ion in lake water samples and recoveries of 100%-103%0 are obtained. The results obtained are found to be in good agreement with spectrophotometric results.

  1. Ethylenediaminium hemioxalate thiocyanate

    Directory of Open Access Journals (Sweden)

    Bohari M. Yamin

    2010-03-01

    Full Text Available In the title compound, C2H10N22+·0.5(C2O42−·NCS−, the ethylenediaminium dication adopts a (+-synclinal conformation with an N—C—C—N torsion angle of 62.64 (15°. The oxalate dianion lies across an inversion centre. In the crystal structure, the ions are linked through N—H...N, N—H...O and C—H...S hydrogen bonds, leading to the formation of a three-dimensional network.

  2. 4-Chloroanilinium thiocyanate

    Directory of Open Access Journals (Sweden)

    Siti Fairus M. Yusoff

    2012-07-01

    Full Text Available In the title compound, C6H7ClN+·NCS−, the benzene ring and the protonated amine and chloro substituents are nearly planar, with a maximum deviation of 0.002 (2 Å for the N atom. In the crystal, the molecules are linked by N—H...N and N—H...S hydrogen bonds into a chain along the b axis.

  3. 4-Chloroanilinium thiocyanate

    OpenAIRE

    Yusoff, Siti Fairus M.; F. Salem Halima; Yamin, Bohari M.

    2012-01-01

    In the title compound, C6H7ClN+·NCS−, the benzene ring and the protonated amine and chloro substituents are nearly planar, with a maximum deviation of 0.002 (2) Å for the N atom. In the crystal, the molecules are linked by N—H...N and N—H...S hydrogen bonds into a chain along the b axis.

  4. Determination of Sodium Thiocyanate Content in Milk by Ion Chromatography%离子色谱法测定乳品中硫氰酸钠含量

    Institute of Scientific and Technical Information of China (English)

    陈基耘

    2014-01-01

    采用离子色谱法测定乳品中硫氰酸钠的含量。样品用5 mL乙腈沉淀蛋白质,上清液过C18柱净化,所得的产物采用离子色谱法测定,外标法定量。结果表明,通过流动相以及前处理方法的改进,硫氰酸钠质量浓度在0.10~4.00 mg/L范围内与色谱峰面积呈良好的线性,相关系数r2=1,方法的检出限为0.01 mg/L。在牛奶样品中加入硫氰酸钠标准溶液进行回收试验,测得回收率为95.0%~101.0%,测定结果的相对标准准偏差为1.8%~2.8%(n=7)。该方法操作简便,能有效避免假阳性的发生,测定结果准确,适合于乳品中硫氰酸钠的检测。%Ion chromatography was applied to the determination of sodium thiocyanate content in milk. The sample was purified by protein precipitation and the C18 extraction column. Then the product was tested by ion chromatography and the concentration was quantified by external standard method. Through the improment of mobile phase and pretreatment method,the concentration of sodium thiocyanate was linear with peak area in the range of 0.10–4.00 mg/L,and the correlation coefficient was r2=1. The detection limit determination of the method was 0.01 mg/L. Test recovery experiment was made by standard addition method,and the recovery was 95.0%–101.0%. The relative standard deviation of the determination results was 1.8%–2.8% (n=7). This method has the advantages of simple operation,it can effectively avoid the occurrence of false positive so it is suitable for detection of sodium thiocyanate in milk.

  5. Determination of ammonium sulphate in ammonia alum by formaldehyde reaction

    Directory of Open Access Journals (Sweden)

    Amir Chand

    1962-01-01

    Full Text Available Existing methods for the estimation of ammonium salts in presence of hydrolysable salts have been reviewed. A new titrimetric method utilizing formaldehyde and potassium fluoride is described for its estimation in presence of aluminium sulphate. The method is accurate and rapid for routine analysis.

  6. Aqueous Media Oxidation of Alcohols with Ammonium Persulfate

    Institute of Scientific and Technical Information of China (English)

    IMANZADEH, Gholam Hassan; ZAMANLOO, Mohammad R.; MANSOORI, Yaghoob; KHODAYARI, Ali

    2007-01-01

    Oxidation of series of various primary and secondary alcohols to corresponding carbonyl compounds with ammonium persulfate in aqueous media was described. No over oxidation of primary alcohols to carboxylic acids and secondary alcohols to esters was observed. Under such conditions benzoin was converted to benzoic acid.

  7. Treating leachate mixture with anaerobic ammonium oxidation technology

    Institute of Scientific and Technical Information of China (English)

    ZHANG Hong-guo; ZHOU Shao-qi

    2006-01-01

    Large amounts of ammonium and a low content of biodegradable chemical oxygen demand(COD) are contained in leachate from aged landfills, together with the effluent containing high concentration of nitric nitrogen after biochemical treatment.Treatment effect of anaerobic ammonium oxidation (anammox) process on the mixture of the leachate and its biochemical effluent was investigated. The results show that the average removal efficiencies of ammonium, nitric nitrogen and total nitrogen are 87.51%,74.95% and 79.59%, respectively, corresponding to the average ratio of removed nitric nitrogen to ammonium, i.e. 1.14 during the steady phase of anammox activity. The mean removal efficiency of COD is only 24.01% during the experimental period. The demand of total phosphorous for the anammox process is unobvious. Especially, the alkalinity and pH value of the effluent are close to those of the influent during the steady phase of anammox activity. In addition, it is demonstrated that the status of the anammox bioreactor can be indicated by the alkalinity and pH value during the course of the experiment. The anammox bioreactor has shown potential for nitrogen removal in the leachate mixture. However, COD and total phosphorous in the leachate mixture need further treatment for removal efficiencies of COD and total phosphorous are not good in the anammox bioreactor.

  8. Characterization of ammonium polyuranate powders from a continuous precipitator

    Energy Technology Data Exchange (ETDEWEB)

    Oolman, T.

    1979-01-01

    Ammonium polyuranate powders produced in a continuous, well-mixed precipitator were characterized by means of electron microscopy. The powders were qualitatively analyzed with the scanning electron microscope and the elementary crystallites were quantivatively analyzed with the transmission electron microscope. The results were fit to a kinetic theory of continuous precipitation. A phase analysis was also preformed by x-ray powder diffraction.

  9. Carboxylates and the uptake of ammonium by excised maize roots

    NARCIS (Netherlands)

    Breteler, H.

    1975-01-01

    The effect of carboxylates (organic acid anions) on NH 4 uptake was studied by changing the carboxylate level of roots prior to uptake experi ments. Succinate was the most effective stimulator of ammonium uptake. The oxocarboxylates (α-oxoglutarate, oxaloacetate and

  10. Fate of N from Green Manures and Ammonium Sulfate

    Institute of Scientific and Technical Information of China (English)

    SHISHU-LIAN; WENQI-XIAO; 等

    1991-01-01

    By means of 15N tracer technique the fate of N in ammonium sulfate,milk vetch,sesbania and azolla,and the availability of their residual N were studied in a microplot experiment.Results showed that a) at the end of the first crop of early rice,both plant recovery and loss of N from ammonium sulfate were the highest whereas those from azolla were the lowest with those from milk vetch and sesbania in between;the sequence was reversed in terms of recovery of N in soil;the net residual N from ammonium sulfate was very low,about 1/7-1/4 of that from green manures,indicating that chemical N fertilizer contributes little to the soil N reserve;b) plant recovery of the residual N was low and it did not always decrease with time;the total plant recovery (from the second to the fifth crops) of the residual N from various test fertilizers was only 8-11% of the total N originally applied;c) the plant recovery of the residual N from ammonium sulfate was the highest,followed by those from milk vetch and sesbania,and that from azolla was the lowest,no matter in which cropping season (from the second to the fifth);N availability ratio showed the same trend,indicating that chemical N fertilizer helps renovate soil organic N,maintain and increase availability of soil N.

  11. Synthetic receptors for ammonium ions using dynamic combinatorial chemistry

    NARCIS (Netherlands)

    Hamieh, Saleh

    2015-01-01

    The general topic of this dissertation is the development of synthetic receptors for organic ammonium ions in near physiological conditions using disulfide dynamic combinatorial chemistry (DCC). Chapter 1 explains the importance of this development and the associated difficulties when using the conv

  12. Characterization of ammonium polyuranate powders from a continuous precipitator

    International Nuclear Information System (INIS)

    Ammonium polyuranate powders produced in a continuous, well-mixed precipitator were characterized by means of electron microscopy. The powders were qualitatively analyzed with the scanning electron microscope and the elementary crystallites were quantivatively analyzed with the transmission electron microscope. The results were fit to a kinetic theory of continuous precipitation. A phase analysis was also preformed by x-ray powder diffraction

  13. Growth features of ammonium hydrogen -tartrate single crystals

    Indian Academy of Sciences (India)

    G Sajeevkumar; R Raveendran; B S Remadevi; Alexander Varghese Vaidyan

    2004-08-01

    Ammonium hydrogen -tartrate (-AHT) single crystals were grown in silica gel. The growth features of these crystals with variation of parameters like specific gravity of the gel, gel pH, acid concentrations, concentration of the feed solution and gel age were studied in detail.

  14. New synthetic method and properties of ammonium dinitramide (ADN)

    Energy Technology Data Exchange (ETDEWEB)

    Hatano, H.; Onda, T.; Shi Ino, K.; Kiname, S.I. [Technical Center, Hosoya Kako, Osawa (Japan); Miyazaki, S.; Suzuki, S. [Research et Development Center, Nissan Motor Co, Saitama (Japan)

    1996-12-31

    Ammonium dinitramide (ADN) is one of the energetic materials, its hazard, however, has never been presented yet. In this paper, new synthetic method of ADN and its properties are contained. It has been found out that ADN has little hazard and is a safe energetic compound. (authors) 4 refs.

  15. 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.)

  16. Increase of water resistance of ammonium nitrate explosives

    Directory of Open Access Journals (Sweden)

    Zulkhair Mansurov

    2012-03-01

    Full Text Available Developed a method of kapsulating of ammonium nitrate with liquid paraffin increase finding explosives in water for 60 minutes. Placing explosives in the plastic shell, the explosive was, as in standing or running water during the day. When conducting field tests failures were absent.

  17. 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 le

  18. Simultaneous Nitrite-Dependent Anaerobic Methane and Ammonium Oxidation Processes

    NARCIS (Netherlands)

    Luesken, F.A.; Sánchez. J.; Van Alen, T.A.; Sanabria, J.; Op den Camp, H.J.; Jetten, M.S.; Kartal, B.

    2011-01-01

    itrite-dependent anaerobic oxidation of methane (n-damo) and ammonium (anammox) are two recently discovered processes in the nitrogen cycle that are catalyzed by n-damo bacteria, including "Candidatus Methylomirabilis oxyfera," and anammox bacteria, respectively. The feasibility of coculturing anamm

  19. Synthesis, DNA binding and cleavage activities of copper (II) thiocyanate complex with 4-( N, N-dimethylamino)pyridine and N, N-dimethylformamide

    Science.gov (United States)

    Chen, Feng-juan; Xu, Min; Xi, Pin-xian; Liu, Hong-yang; Zeng, Zheng-zhi

    2011-10-01

    Two novel copper(II) thiocyanate complexes with 4-( N, N-dimethylamino) pyridine and N, N-dimethylformamide( 1) and with4-( N, N-dimethylamino) pyridine ( 2) have been synthesized and characterized. The crystal and molecular structures of complexes 1 and 2 were determined by single-crystal X-ray diffraction. Antioxidative activity tests in vitro showed that complex 1 has significant antioxidative activity against hydroxyl free radicals from the Fenton reaction and also oxygen free radicals, which is better than standard antioxidants like vitamin C and mannitol. The interaction of complex 1 with calf thymus DNA was investigated by spectroscopic, cyclic voltammetry, and viscosity measurements. Results suggest that complex 1 can bind to DNA via partial intercalation mode. Moreover, complex 1 has been found to cleavage of plasmid DNA pBR322.

  20. Atomic force microscopy studies on growth mechanisms and defect formations on {l_brace}110{r_brace} faces of cadmium mercury thiocyanate crystals

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, X.N.; Xu, D.; Yuan, D.R.; Sun, D.L.; Lu, M.K.; Zhang, G.H.; Guo, S.Y. [Shandong Univ., Jinan, SD (China). Inst. of Crystal Materials

    2001-07-01

    Growth mechanisms and defect formations on {l_brace}110{r_brace} faces of cadmium mercury thiocyanate crystals grown at 30 C ({sigma} = 0.24) were investigated by using atomic force microscopy (AFM). It was found that, under this condition, spiral dislocation controlled mechanism and 2D nucleation mechanism operates simultaneously and equally during growth, which is completely different from the traditional 2D nucleation and dislocation source controlled mechanisms. A number of 2D nucleus are formed at the large step terraces generated by dislocation sources, leading to the unequal growth rates of the elementary steps and thereby ''step bunches'' are caused. Various defects are formed under this growth condition, which is assumed to result from the incongruence between the steps generated by different sources. A new kind of 2D defect, corresponding to one growth layer in height, was observed for the first time. (orig.)

  1. The influence of H-bonding on the 'ambidentate' coordination behaviour of the thiocyanate ion to Cd(II): a combined experimental and theoretical study.

    Science.gov (United States)

    Hazari, Alokesh; Das, Lakshmi Kanta; Bauzá, Antonio; Frontera, Antonio; Ghosh, Ashutosh

    2014-06-01

    Two new trinuclear hetero-metallic copper(II)-cadmium(II) complexes [(CuL)2Cd(NCS)2] (1) and [(CuL(R))2Cd(SCN)2] (2) have been synthesized using [CuL] and [CuL(R)] as "metalloligands" (where H2L = N,N'-bis(salicylidene)-1,4-butanediamine and H2L(R) = N,N'-bis(2-hydroxybenzyl)-1,4-butanediamine) respectively. Both the complexes were characterized by elemental analysis, various spectroscopic methods and single crystal XRD. Complex 1 is an angular trinuclear species, in which two terminal four-coordinate square planar "metalloligands" [CuL] are coordinated to a central Cd(II) through double phenoxido bridges along with two mutually cis nitrogen atoms of terminal thiocyanate ions. In complex 2, which is linear, in addition to the double phenoxido bridge, two SCN(-) coordinate to the trans positions of the central octahedral Cd(II) via S atoms. Theoretical calculations on the energetic difference between the two possible coordination modes of the thiocyanate anion to the Cd atom reveal that N-coordination is preferred over S-coordination in agreement with the much greater abundance of the reported N-bonded structures. In 2, there is a strong N-H···NCS-Cd H-bonding interaction, the binding energy of which is computed to be approximately -9.3 kcal mol(-1), which is sufficient to compensate the 9.0 kcal mol(-1) of energetic cost due to the unusual Cd-SCN coordination mode. PMID:24715108

  2. Studies on Solvent Sublation of Trace Heavy Metals by Continuous Flow System as Ternary Complexes of 1,10-Phenanthroline and Thiocyanate Ion

    International Nuclear Information System (INIS)

    A continuous flow system has been developed to determine trace Cu(II), Mn(II), Ni(II) and Zn(II) in a large volume of water samples by a solvent sublation technique. The mixed solution of 1,10-phenanthroline(phen) and thiocyanate ion was used as ligands for the formation of their ternary complexes. The continuous system was constructed in this laboratory with a peristaltic pump, a mini shaker, three mixing bottles and a flotation cell by connecting each part with a polyethylene tube. The flotation conditions such as the flow rate of sample solution and the injection rates of ligand, buffer and surfactant solutions have been investigated to obtain the best sublation efficiencies. Each solution flowed into the flotation cell through each polyethylene tube by the peristaltic pumps. The ternary complexes were floated and extracted into MIBK in a flotation cell of 2 L by bubbling a nitrogen gas. The absorbances of extracted analytes in MIBK were directly measured by graphite furnace-AAS. The concentrations of 1,10-phenanthroline and thiocyanate ion were 2.6 x 10-3 M and 2.3 x 10-2 M in the mixed solution, respectively. The pH of sample solution was adjusted to 5.0 with a buffer solution and 1%(m/v) sodium lauryl sulphate solution was added as a surfactant to support the effective flotation of the complexes. The N2 gas was bubbled at 30 mL/min for 90 minutes for 20 L of sample. Reproducible results of less than 10% RSD and recoveries of 80-120% could be obtained in real samples

  3. Antibacterial activity of reactive quaternary ammonium compounds in solution and in nonleachable coatings

    NARCIS (Netherlands)

    Gozzelino, G.; Romero Tobar, D.E.; Chaitiemwong, N.; Hazeleger, W.C.; Beumer, R.R.

    2011-01-01

    Antibacterial polymers suitable for coating applications without leaching of the biocidal component have been obtained by UV copolymerization of acrylic resins with acrylic monomers containing quaternary ammonium moieties. Suitable reactive biocides, based on quaternary ammonium monomers (QAMs), end

  4. 76 FR 39847 - Solid Fertilizer Grade Ammonium Nitrate From the Russian Federation; Final Results of the...

    Science.gov (United States)

    2011-07-07

    ...: Solid Fertilizer Grade Ammonium Nitrate From the Russian Federation, 64 FR 45236 (August 19, 1999). On... Fertilizer Grade Ammonium Nitrate From the Russian Federation, 65 FR 42669 (July 11, 2000) (``Final... International Trade Administration Solid Fertilizer Grade Ammonium Nitrate From the Russian Federation;...

  5. 77 FR 65532 - Solid Fertilizer Grade Ammonium Nitrate From the Russian Federation: Notice of Rescission of...

    Science.gov (United States)

    2012-10-29

    ... International Trade Administration Solid Fertilizer Grade Ammonium Nitrate From the Russian Federation: Notice... the antidumping duty order on solid fertilizer grade ammonium nitrate (ammonium nitrate) from the... Nitrate from Russia: Correction to Notice of Opportunity to Request Administrative Review, 77 FR...

  6. 40 CFR 721.10100 - Dialkyl dimethyl ammonium carbonate (2:1) (generic).

    Science.gov (United States)

    2010-07-01

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

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

    Directory of Open Access Journals (Sweden)

    G. D. Song

    2013-03-01

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

  8. 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

  9. 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.

  10. Synthesis, antimicrobial activity of lamotrigine and its ammonium derivatives

    Indian Academy of Sciences (India)

    Yong Qian; Peng-Cheng Lv; Lei Shi; Rui-Qin Fang; Zhong-Cheng Song; Hai-Liang Zhu

    2009-07-01

    Antiepileptic drug lamotrigine and its thirteen ammonium salt complexes (4a-4m) were synthesized and characterized by IR, elemental analysis, 1H-NMR, and MS spectral methods. Many of the ammonium salts (4a-4m) were first reported. Furthermore, the crystal structure of compound 3 was determined by single crystal X-ray diffraction analysis. All these complexes were tested in vitro for their antibacterial activity (Bacillus subtilis, Staphylococcus aureus, Enterococus faecalis, Escherichia coli, Pseudomonas aeruginosa and Enterobacter cloacae). The results indicated that most of the complexes showed good antibacterial activity against Gram-positive (B. subtilis, S. aureus and S. faecalis), but showed mild, even inactive against Gram-negative bacterial strains.

  11. Recent Advances in the Synthesis of Ammonium-Based Rotaxanes

    Directory of Open Access Journals (Sweden)

    Dominic Thibeault

    2010-05-01

    Full Text Available The number of synthetic methods enabling the preparation of ammonium-based rotaxanes has increased very rapidly in the past ten years. The challenge in the synthesis of rotaxanes results from the rather weak interactions between the ammonium-containing rod and the crown ether macrocycle in the pseudorotaxane structure that rely mostly on O•H hydrogen bonds. Indeed, no strong base or polar solvent that could break up H-bonding can be used during the formation of rotaxanes because the two components will separate as two distinct entities. Moreover, most of the reactions have to be performed at room temperature to favor the formation of pseudorotaxane in solution. These non-trivial prerequisites have been taken into account to develop efficient reaction conditions for the preparation of rotaxanes and those are described in detail along this review.

  12. Thermal stability assessment of anti-explosive ammonium nitrate

    Institute of Scientific and Technical Information of China (English)

    Lijin Shen; Xuguang Wang

    2005-01-01

    The explosivity experiment of anti-explosive ammonium nitrate (AEAN) shows that the explosive characteristic of AEAN is eliminated. The adiabatic decompositions of ammonium nitrate and AEAN were investigated with an accelerating rate calorimeter (ARC). The curves of thermal decomposition temperature and pressure versus time, self-heating rate and pressure versus temperature for two systems were obtained. The kinetic parameters such as apparent activation energy and pre-exponential factor were calculated.The safety of AEAN was analyzed. It was indicated that AEAN has a higher thermal stability than AN. At the same time, it can be shown that the elimination of its explosive characteristic is due to the improvement on the thermal stability of AEAN.

  13. EXCHANGE ADSORPTION EQUILIBRIA OF AMMONIUM ON CATION-VERMICULITE MINERALS

    Institute of Scientific and Technical Information of China (English)

    GUO Yaping; XIE Lianwu; WU Xiaofu

    2006-01-01

    Experiment was designed under different pH and temperature conditions to analysis the NH4+ exchange capacity of Na+-vermiculite, Ca2+-vermiculite and Mg2+-vermiculite clay minerals pre-treated using NaCl, CaCl2 and MgCl2 solutions respectively. The results indicated that the exchange reactions occurred most rapidly at the proceeding 80 minutes and approached to equilibrium by about 120 minutes. The exchange quantity of ammonium on the vermiculite (at initial ammonium concentration of 673mg/L ) varied with pH with a peak value of 28.36mg/g on Na+-vermiculite, 23.01mg/g on Ca2+-vermiculite, 20.14mg/g on Mg2+-vermiculite, 18.04mg/g on natural vermiculite at pH 7. The exchange and adsorption isotherm of NH4+ on cation-vermiculite can be described by Langmuir equation.

  14. Kinetic study of uranium residue dissolution in ammonium carbonate media

    International Nuclear Information System (INIS)

    The purpose of this study was to determine the kinetics of the dissolution of a uranium residue in ammonium carbonate media. The residue is generated in the production of medical isotopes. The effects of parameters, such as varying peroxide and carbonate concentrations, dissolution time as well as temperature on the extraction rate have been separately studied. Results indicate complete dissolution of the residue at 60 deg C, after 30 min, in ammonium carbonate solution enriched with hydrogen peroxide. The yield and rate of uranium extraction were found to increase as a function of both temperature, in the range of 25-60 deg C, and hydrogen peroxide concentration. The extraction process was governed by chemical reaction as the activation energy was found to be 45.5 kJ/mol. The order of reaction with respect to uranium concentration was found to be approximately first order. (author)

  15. Anaerobic ammonium oxidation in a bioreactor treating slaughterhouse wastewater

    Directory of Open Access Journals (Sweden)

    V. Reginatto

    2005-12-01

    Full Text Available Ammonium oxidation was thought to be an exclusively aerobic process; however, as recently described in the literature, it is also possible under anaerobic conditions and this process was named ANAMMOX. This work describes the operation of a system consisting of a denitrifying reactor coupled to a nitrifying reactor used for removal of nitrogen from slaughterhouse wastewater. During operation of the denitrifying reactor an average nitrogen ammonium removal rate of 50 mg/Ld was observed. This biomass was used to seed a second reactor, operated in repeated fed batch mode, fed with synthetic medium specific to the growth of bacteria responsible for the ANAMMOX process. The nitrogen loading rate varied between 33 and 67 mgN/Ld and average nitrogen removal was 95% and 40%, respectively. Results of fluorescence in situ hybridization (FISH confirmed the presence of anammox-like microorganisms in the enriched biomass.

  16. 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.

  17. Synthesis and characterization of ammonium phosphate fertilizers with boron

    OpenAIRE

    ANGELA MAGDA; RODICA PODE; CORNELIA MUNTEAN; MIHAI MEDELEANU; ALEXANDRU POPA

    2010-01-01

    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 ...

  18. 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.

  19. Nitrogen loss by anaerobic oxidation of ammonium in rice rhizosphere

    OpenAIRE

    Nie, San'an; Li, Hu; Yang, Xiaoru; Zhang, Zhaoji; Weng, Bosen; Huang, Fuyi; Zhu, Gui-Bing; Zhu, Yong-Guan

    2015-01-01

    Anaerobic oxidation of ammonium (anammox) is recognized as an important process for nitrogen (N) cycling, yet its role in agricultural ecosystems, which are intensively fertilized, remains unclear. In this study, we investigated the presence, activity, functional gene abundance and role of anammox bacteria in rhizosphere and non-rhizosphere paddy soils using catalyzed reporter deposition–fluorescence in situ hybridization, isotope-tracing technique, quantitative PCR assay and 16S rRNA gene cl...

  20. Recovering germanium from coal ash by chlorination with ammonium chloride

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A new process of enriching germanium from coal ash was developed. The process involves in mixing the coal ash and ammonium chloride and then roasting the mixture to produce germanium chloride that is then absorbed by dilute hydrochloric acid and hydrolyzed to germanium oxide. The germanium recovery reached to 80.2% at the optimum condition: mass ratio of NH4Cl/coal ash is 0.15, roasting temperature 400℃ and roasting time 90 min.

  1. Ammonium Uptake by Phytoplankton Regulates Nitrification in the Sunlit Ocean

    OpenAIRE

    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 throu...

  2. 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. PMID:25613641

  3. Hibiscus sabdariffa Affects Ammonium Chloride-Induced Hyperammonemic Rats

    OpenAIRE

    Subramanian, P.; M. Mohamed Essa

    2007-01-01

    Hibiscus sabdariffa (HS) is an edible medicinal plant, indigenous to India, China and Thailand and is used in Ayurveda and traditional medicine. Alcoholic extract of HS leaves (HSEt) was studied for its anti-hyperammonemic and antioxidant effects in brain tissues of ammonium chloride-induced hyperammonemic rats. Oral administration of HSEt (250 mg kg−1 body weight) significantly normalizes the levels of ammonia, urea, uric acid, creatinine and non-protein nitrogen in the blood. HSEt significa...

  4. Subsurface ammonium maxima in northern Bay of Bengal

    Digital Repository Service at National Institute of Oceanography (India)

    Satyanarayana, D.; Sahu, S.D.; Panigrahy, P.K.; Sarma, V.V.; Suguna, C.

    . Inorganic phosphate was determined by the method of Murphy & Riley (1962), nitrite by the method of Bendschneider & Robinson (1952) and nitrate by the method of Morris & Riley (1963) as modified by Grasshoff (1964). Ammonium was determined by indophenol.... Further, its distribution in the water column showed no definite vertical trend as reported earlier in the other open oceans (Menzel & Spaeth, 1962; Sagi, 1966). However, in the northern Bay of Bengal two prominent maxima, one in the euphotic zone near...

  5. Alicyclic ammonium ionic liquids as lithium battery electrolytes A review

    OpenAIRE

    Puga, A.V.

    2013-01-01

    Ionic liquids are reasonable alternatives to electrolytes used in energy storage devices, such as lithium batteries, both lithium-ion and lithium-metal, given the safety advantages they provide. This is due to the favourable properties they often possess, mainly non­flammability and non­volatility. Candidates with alicyclic ammonium cations exhibit high electrochemical stabilities, especially towards lithium, a unique feature which enables the fabrication of reversible lithium-metal batteries...

  6. Nitrogen addition regulates soil nematode community composition through ammonium suppression.

    Directory of Open Access Journals (Sweden)

    Cunzheng Wei

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

  7. Study of stripping cristallization processus of AUC with ammonium carbonate

    International Nuclear Information System (INIS)

    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 (NH4)2CO3. The effects of operating conditions ((NH4)2CO3 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 (NH4)2CO3 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 (NH4)2CO3 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

  8. Extraction Factor Of Pure Ammonium Paratungstate From Tungsten Scraps

    Directory of Open Access Journals (Sweden)

    Pee J.-H.

    2015-06-01

    Full Text Available Typical oxidation process of tungsten scraps was modified by the rotary kiln with oxygen burner to increase the oxidation rate of tungsten scraps. Also to accelerate the solubility of solid oxidized products, the hydrothermal reflux method was adapted. By heating tungsten scraps in rotary kiln with oxygen burner at around 900° for 2hrs, the scraps was oxidized completely. Then oxidized products (WO3 and CoWO4 was fully dissolved in the solution of NaOH by hydrothermal reflux method at 150° for 2hrs. The dissolution rate of oxidized products was increased with increasing the reaction temperature and concentration of NaOH. And then CaWO4 and H2WO4 could be generated from the aqueous sodium tungstate solution. Ammonium paratungstate (APT also could be produced from tungstic acid using by aqueous ammonium solution. The morphologies (cubic and plate types of APT was controlled by the stirring process of purified solution of ammonium paratungstate.

  9. Structural basis for Mep2 ammonium transceptor activation by phosphorylation.

    Science.gov (United States)

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

    2016-04-18

    Mep2 proteins are fungal transceptors that play an important role as ammonium sensors in fungal development. Mep2 activity is tightly regulated by phosphorylation, but how this is achieved at the molecular level is not clear. Here we report X-ray crystal structures of the Mep2 orthologues from Saccharomyces cerevisiae and Candida albicans and show that under nitrogen-sufficient conditions the transporters are not phosphorylated and present in closed, inactive conformations. Relative to the open bacterial ammonium transporters, non-phosphorylated Mep2 exhibits shifts in cytoplasmic loops and the C-terminal region (CTR) to occlude the cytoplasmic exit of the channel and to interact with His2 of the twin-His motif. The phosphorylation site in the CTR is solvent accessible and located in a negatively charged pocket ∼30 Å away from the channel exit. The crystal structure of phosphorylation-mimicking Mep2 variants from C. albicans show large conformational changes in a conserved and functionally important region of the CTR. The results allow us to propose a model for regulation of eukaryotic ammonium transport by phosphorylation.

  10. Increasing wheat production while decreasing nitrogen losses from ammonium bicarbonate

    International Nuclear Information System (INIS)

    The objectives of a 4-year field experiment were i) to investigate the effects of rate and timing of application of ammonium bicarbonate on N-uptake efficiency by irrigated winter wheat, ii) to determine the fate of fertilizer N in wheat followed by maize, and iii) to study nitrate dynamics in the soil after N-fertilizer application to evaluate groundwater pollution by leaching. Nitrogen-application rates significantly affected wheat grain yields and straw dry matter. Grain yields were higher with 150 than with 225 kg N ha-1, whereas the highest fractional recoveries of N from ammonium bicarbonate occurred with 75 kg N ha-1 (38.5% in 1994-95 and 33.5% in 1996-97). On the basis of grain yield, N recovery and soil-N balance, ammonium bicarbonate at 150 kg N ha-1, was the optimum rate, when applied basally and as a top dressing to wheat. Subsequent yields of maize stover and grain were affected by N applied to the wheat, suggesting that fertilizer recommendations, in terms of rate and timing, should be made on the basis of effects on the cropping rotation as a whole. Water-holding capacity of the soil was poor, therefore large applications of N are likely to cause nitrate pollution of ground water. (author)

  11. Concurrence of Anaerobic Ammonium Oxidation and Organotrophic Denitrification in Presence of p-Cresol.

    Science.gov (United States)

    González-Blanco, G; Cervantes, F J; Beristain-Cardoso, R; Gómez, J

    2015-08-01

    This study was carried out to evaluate the capacity of anaerobic granular sludge for oxidizing ammonium and p-cresol with nitrate as terminal electron acceptor. Kinetics for the anaerobic oxidation of ammonium and p-cresol is described in this paper. The phenolic compound was very efficiently consumed, achieving 65 % of mineralization. Ammonium and nitrate were also consumed at 83 and 92 %, respectively, being the main product N2. Anaerobic ammonium oxidation was promoted owing to accumulation of nitrite, and it allowed the synergy of anaerobic ammonium oxidation and organotrophic denitrification for the simultaneous removal of ammonium, nitrate, and p-cresol. A carbonaceous intermediate partially identified was transiently accumulated, and it transitorily truncated the respiratory process of denitrification. These experimental results might be considered for defining strategies in order to remove nitrate, ammonium, and phenolic compounds from wastewaters. PMID:26062920

  12. 乳制品中硫氰酸钠快速检测方法的优化%Improvement on the Rapid Detection Method of Sodium Thiocyanate in Dairy Products

    Institute of Scientific and Technical Information of China (English)

    尚欣春; 高志莹; 洪霞; 冯玉升

    2012-01-01

    This paper studied improvement on a method for rapid determination of sodium thiocyanate in dairy products. On the basis of the color of the orihinal color trivalent iron ions, the indicator crystal violet and rhodamine b were introduced. The results showed that in the qualitative detection of sodium thiocyanate color, after the introduction of indicatior, the target content of dairy products with less color re- sults was easier to distinguish, which could improve the accuracy and sensitivity of sodium thiocyanate qualitative test.%研究了乳制品中硫氰酸钠的快速检测方法及方法的改进。在原本显色剂三价铁离子显色的基础上,引入了指示剂结晶紫、罗丹明B。结果表明,在硫氰酸钠显色定性检测中,引入指示剂后,目标物含量较少的乳制品显色结果更易分辨,提高了硫氰酸钠定性试验的准确度和灵敏度。

  13. Separation and purification of sodium thiocyanate by ceramic membrane filtration%陶瓷膜分离净化硫氰酸钠工艺研究

    Institute of Scientific and Technical Information of China (English)

    顾文兰

    2012-01-01

    Sodium thiocyanate as a solvent for wet-spun acrylic fiber was separated and purified by ceramic membrane technique. The attenuation trend of membrane flux with operation time and the relationship between concentration multiple and membrane flux attenuation were analyzed. The membrane flux recovery method was decided. The separation effect and characteristics of different membrane tubes were compared. The results showed that ceramic membrane was able to effectively clean the impurities in sodium thiocyanate and the removal rate of water insoluble substance was above 75% ; the membrane flux was decreased with the increase of operation time, and the membrane flux can be recovered by washing with pure hot water when the average membrane flux was lower than the designed value; the membrane tubes should be replaced or treated by some chemical techniques when the membrane flux can not be recovered by pure hoi water washing; the membrane thickness did not have great effect on membrane flux, but the thicker membrane provided better impurity cleaning effect.%采用陶瓷膜分离净化湿法腈纶溶剂硫氰酸钠物料,分析了膜通量随运行时间的衰减变化趋势及浓缩倍数与膜通量衰减的关系,确定了恢复膜通量的方法,比较了不同膜管的分离效果和分离特性.结果表明:陶瓷膜能有效截留硫氰酸钠物料中的杂质,水不溶物去除率大于75%;膜通量都随运行时间的延长而衰减,当平均膜通量低于设计膜通量时,可采用热纯水进行洗脱,使膜通量恢复;当热纯水无法使膜通量恢复,可采用化学方法或更换膜管;不同膜层厚度的膜管对膜通量影响不大,但厚层膜管的分离除杂效果好.

  14. 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.

  15. Regeneration of clinoptilolite zeolite used for the ammonium removal

    International Nuclear Information System (INIS)

    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 (Mg2+) and calcium (Ca2+) 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)

  16. A study on stability of erythromycin thiocyanate in acid solution%硫氰酸红霉素在酸性溶液中的稳定性研究

    Institute of Scientific and Technical Information of China (English)

    毛培学; 陈葵; 纪利俊; 朱家文

    2013-01-01

    硫氰酸红霉素的生产是通过在酸性条件下反应结晶的方式制备,其稳定性直接影响产品的纯度.本文用磷酸缓冲盐溶液调节反应体系的pH,研究了硫氰酸红霉素各组分的降解率随pH的变化.结果表明,在硫氰酸红霉素的A、B、C3种组分中,以活性组分A的稳定性受pH值的影响最大;pH在4.5时,硫氰酸红霉素A能够在40min内保持稳定,超过40min会发生降解;而当pH小于4.0时,硫氰酸红霉素A组分发生快速降解.文章探讨了红霉素A的降解机理,并研究了等摩尔硫氰酸根条件下红霉素A组分降解动力学,得到的模型rA=1.93×104CAC[H]1.59与实验结果吻合良好,与文献对比,说明等摩尔硫氰酸根的存在降低了红霉素A的降解速率.%Erythromycin thiocyanate is producted in acid solution by reactive crystallization method, whose purity is effected by its acid stability. In this paper, pH was regulated by phosphate buffer and the stabilities of components of erythromycin thiocyanate under different pH were researched. The results show that during the three components of erythromycin thiocyanate, A, B and C, pH has the largest effect on the stability of A. When the pH is 4.5, erythromycin thiocyanate A can be steady in 40min and then will degradate; when pH is under 4.0, erythromycin thiocyanate A will degradate fastly. The degradation mechanism is stated, at the same time, the degradation kinetics of erythromycin A when [SCN]" exist in acid solution was also described by equation rA = 1.93 × 104 CAC159[H]+ , which is found to be in line with the experimental results. Compared with the result that without [SCN]\\ a conclusion that degradation rate of erythromycin A is droped by [SCN]".

  17. 聚合后功能化法合成硫氰液晶高分子及其表征%Synthesis and Characterization of Thiocyanic Liquid Crystal Polymer by Post-polymerization Functionalization

    Institute of Scientific and Technical Information of China (English)

    王彩虹; 谭帅; 刘卫东; 梁婷; 伍勇

    2013-01-01

    A side-chain liquid crystal polymer(3) containing modifiable bromo groups at the terminal site of side chains was prepared by radical polymerization. Thiocyanic liquid crystal polymer(6Ⅰ ) was synthesized successfully by post-polymerization functionalization of 3(the brominated precursor) to give liquid crystal polymer(5) containing modifiable bromo groups, then substituted Br in 5 with thiocyanic salt. Another thiocyanic liquid crystal polymer(6Ⅱ ) was also synthesized by radical polymerization of a thiocyanic monomer (4) containing a mesogenic unit which was obtained from 3 by front-polymerization functionalization with thiocyanic salt. The structures were characterized by 1H NMR and IR. The chemical structures of 6Ⅰ and 6Ⅱwere identical. However, molecular weight of 6Ⅰ was higher than 6Ⅱ . 6Ⅰ and 6Ⅱ exhibited bi-layered Smectic A phase over a broad temperature range by polarized optical microscopy, differential scanning calorimeter and XRD.%采用自由基聚合制备了侧链末端含溴的可修饰性液晶高分子(3),以3为前体用硫氰酸盐进行聚合后功能化成功地合成了硫氰液晶高分子(6Ⅰ);以3为前体采用聚合前功能化先制得含液晶基元的硫氰单体(4);再通过自由基聚合反应合成硫氰液晶高分子(6Ⅲ).其结构经1H NMR和IR表征,6Ⅰ和6Ⅲ具有相同的化学结构,6Ⅰ的分子量更高.偏光显微镜、差示扫描量热和X-射线衍射分析结果表明,6Ⅰ和6Ⅲ在较宽温度范围内均表现出双分子层的近晶A相.

  18. 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.

  19. 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.

  20. Experimental study of the detonation of technical grade ammonium nitrate

    Science.gov (United States)

    Presles, Henri-Noël; Vidal, Pierre; Khasainov, Boris

    2009-11-01

    The detonation of technical grade ammonium nitrate at the density ρ=0.666 g/cm confined in PVC and steel tubes was experimentally studied. The results show that the detonation is self-sustained and steady in steel tubes with diameter as small as 12 mm. Critical detonation diameter lies between 8 and 12 mm in 2 mm thick steel tubes and between 55 and 81 mm in PVC tubes. These values testify a strong detonation sensitivity of this product. To cite this article: H.-N. Presles et al., C. R. Mecanique 337 (2009).

  1. Aluminum-silicates flotation with quaternary ammonium salts

    Institute of Scientific and Technical Information of China (English)

    王毓华; 胡岳华; 陈湘清

    2003-01-01

    The zeta potential measurements show that the flotation separation of diaspore from kaolinite, illite and pyrophyllite could be achieved in the range of pH 46.5 with cationic collectors. A special quaternary ammonium salts(DTAL) shows better selectivity than that the dodecyl amine(DDA) does for the flotation of three silicates. The closed-circuit flotation results show that the reverse flotation de-silicate can be achieved with DTAL as collector, a new inorganic reagent(SFL) as depressant and MIBC as frother to obtain a bauxite concentrate m(Al2O3)/m(SiO2)>10, Al2O3 recovery>86%).

  2. Prediction of Particle Size of Ammonium Perchlorate during Pulverisation

    Directory of Open Access Journals (Sweden)

    Sunil Jain

    2006-07-01

    Full Text Available Ammonium perchlorate has been pulverised by an impact mill (air classifier mill to studythe influence of different operating parameters, viz., effect of mill speed, classifier speed, feedrate, and damper opening (suction rate on the particle size. Further based on the differentgrinding parameters, an empirical equation has been developed and used for the prediction ofparticle size. The experimental results indicate that the values are very close to the predictedones. In addition, particle size distribution has also been studied by applying different modelequations and it has been found that Rosin-Rammler model is the most suitable model for thisoperation.

  3. Ammonium sulphate on maize crops under no tillage

    OpenAIRE

    Maria Anita Gonçalves da Silva; Anny Rosi Mannigel; Antonio Saraiva Muniz; Simone Maria Altoé Porto; Marlene Estevão Marchetti; Antonio Nolla; Rosemary Marques de Almeida Bertani

    2012-01-01

    The objectives of this work were to evaluate the management of N and S (as ammonium sulphate) fertilization under no-tillage system on the components of maize productivity and on N and S accumulation in the crop, as well as to evaluate the minimum value of the Nitrogen Sufficiency Index (NSI 0.95) as an indicator for side dressing requirements. The experiment had a completely randomized block design with six treatments and four replications carried out in Red Latosol dystrophic soil (Hapludox...

  4. Further laboratory and theoretical investigations of ammonium dinitramide

    Energy Technology Data Exchange (ETDEWEB)

    Tulis, A.J.; Snelson, A. [IIT Research Institut, Chicago (United States); Heberlein, C.; Patel, D.L. [U.S. Army Cecom RD et E Center, NVESD (United States)

    1996-12-31

    Hydrogen and deuterated ammonium dinitramide have been vaporized under high vacuum and the IR matrix isolation spectra of the decomposition products obtained. Tentative vibration assignments have been made for HN(NO{sub 2}){sub 2} and DN(NO{sub 2}){sub 2} assuming a symmetrical non-planar structure in which the H or D is bonded to the central nitrogen atom. Other structures are also possible. Ab initio calculations have been made for the various structural isomers of hydrogen dinitramide. Vibration frequencies calculated for the hydrogenated and deuterated species are compared with the experimental values with the object of identifying the molecules` structure. (authors) 3 refs.

  5. 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.)

  6. Solution-processed inorganic copper(I) thiocyanate (CuSCN) hole transporting layers for efficient p–i–n perovskite solar cells

    KAUST Repository

    Zhao, Kui

    2015-08-27

    CuSCN is a highly transparent, highly stable, low cost and easy to solution process HTL that is proposed as a low cost replacement to existing organic and inorganic metal oxide hole transporting materials. Here, we demonstrate hybrid organic-inorganic perovskite-based p-i-n planar heterojunction solar cells using a solution-processed copper(I) thiocyanate (CuSCN) bottom hole transporting layer (HTL). CuSCN, with its high workfunction, increases the open circuit voltage (Voc) by 0.23 V to 1.06 V as compared with devices based on the well-known poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) (0.83 V), resulting in a superior power conversion efficiency (PCE) of 10.8% without any notable hysteresis. Photoluminescence measurements suggest a similar efficiency of charge transfer at HTL/perovskite interface as PEDOT:PSS. However, we observe more efficient light harvesting in the presence of CuSCN at shorter wavelengths despite PEDOT:PSS being more transparent. Further investigation of the microstructure and morphology reveals differences in the crystallographic texture of the polycrystalline perovskite film, suggesting somewhat modified perovskite growth on the surface of CuSCN. The successful demonstration of the solution-processed inorganic HTL using simple and low temperature processing routes bodes well for the development of reliable and efficient flexible p-i-n perovskite modules or for integration as a front cell in hybrid tandem solar cells.

  7. Glass transition dynamics and conductivity scaling in ionic deep eutectic solvents: The case of (acetamide + lithium nitrate/sodium thiocyanate) melts

    Energy Technology Data Exchange (ETDEWEB)

    Tripathy, Satya N., E-mail: satyanarayantripathy@gmail.com; Wojnarowska, Zaneta; Knapik, Justyna; Paluch, Marian [Institute of Physics, University of Silesia, Uniwersytecka 4, 40-007 Katowice (Poland); Silesian Center for Education and Interdisciplinary Research, 75 Pulku Piechoty 1A, 41-500 Chorzow (Poland); Shirota, Hideaki [Department of Nanomaterial Science and Department of Chemistry, Chiba University, 1-33 Yayoi, Inage-ku, Chiba 263-8522 (Japan); Biswas, Ranjit [Department of Chemical, Biological and Macromolecular Sciences, S. N. Bose National Centre for Basic Sciences, JD Block, Sector III, Salt Lake, Kolkata 700098 (India)

    2015-05-14

    A detailed investigation on the molecular dynamics of ionic deep eutectic solvents (acetamide + lithium nitrate/sodium thiocyanate) is reported. The study was carried out employing dielectric relaxation spectroscopy covering seven decades in frequency (10{sup −1}-10{sup 6} Hz) and in a wide temperature range from 373 K down to 173 K, accessing the dynamic observables both in liquid and glassy state. The dielectric response of the ionic system has been presented in the dynamic window of modulus formalism to understand the conductivity relaxation and its possible connection to the origin of localized motion. Two secondary relaxation processes appear below glass transition temperature. Our findings provide suitable interpretation on the nature of secondary Johari-Goldstein process describing the ion translation and orientation of dipoles in a combined approach using Ngai’s coupling model. A nearly constant loss feature is witnessed at shorter times/lower temperatures. We also discuss the ac conductivity scaling behavior using Summerfield approach and random free energy barrier model which establish the time-temperature superposition principle. These experimental observations have fundamental importance on theoretical elucidation of the conductivity relaxation and glass transition phenomena in molten ionic conductors.

  8. Phase Behaviour of 1-Ethyl-3-methylimidazolium Thiocyanate Ionic Liquid with Catalytic Deactivated Compounds and Water at Several Temperatures: Experiments and Theoretical Predictions

    Directory of Open Access Journals (Sweden)

    Ramalingam Anantharaj

    2011-01-01

    Full Text Available Density, surface tension and refractive index were determined for the binary mixture of catalytic deactivated compounds with 1-ethyl-3-methylimidazolium thiocyanate {[EMIM][SCN]} at temperature of (298.15 to 323.15 K. For all the compounds with ILs, the densities varied linearly in the entire mole fraction with increasing temperature. From the obtained data, the excess molar volume and deviation of surface tension and refractive index have been calculated. A strong interaction was found between similar (cation-thiophene or cation-pyrrole compounds. The interaction of IL with dissimilar compounds such as indoline and quinoline and other multiple ring compounds was found to strongly depend on the composition of IL at any temperatures. For the mixtures, the surface tension decreases in the order of: thiophene > quinoline > pyridine > indoline > pyrrole > water. In general from the excess volume studies, the IL-sulphur/nitrogen mixture has stronger interaction as compared to IL-IL, thiophene-thiophene or pyrrole-pyrrole interaction. The deviation of surface tension was found to be inversely proportional to deviation of refractive index. The quantum chemical based COSMO-RS was used to predict the non-ideal liquid phase activity coefficient for all mixtures. It indicated an inverse relation between activity coefficient and excess molar volumes.

  9. Anti-inflammatory drugs interacting with Zn (II) metal ion based on thiocyanate and azide ligands: Synthesis, spectroscopic studies, DFT calculations and antibacterial assays

    Science.gov (United States)

    Chiniforoshan, Hossein; Tabrizi, Leila; Hadizade, Morteza; Sabzalian, Mohammad R.; Chermahini, Alireza Najafi; Rezapour, Mehdi

    2014-07-01

    Zinc (II) complexes with non-steroidal anti-inflammatory drugs (NSAIDs) naproxen (nap) and ibuprofen (ibu) were synthesized in the presence of nitrogen donor ligands (thiocyanate or azide). The complexes were characterized by elemental analysis, FT-IR, 1H NMR and UV-Vis spectroscopes. The binding modes of the ligands in complexes were established by means of molecular modeling of the complexes, and calculation of their IR, NMR and absorption spectra at DFT (TDDFT)/B3LYP level were studied. The experimental and calculated data verified monodentate binding through the carboxylic oxygen atoms of anti-inflammatory drugs in the zinc complexes. The calculated 1H, FT-IR and UV-Vis data are in better agreement with the experimental results, and confirm the predicted tetrahedral structures for the Zn (II) complexes. In addition to DFT calculations of complexes, natural bond orbital (NBO) was performed at B3LYP/6-31+G(d,p) level of theory. Biological studies showed the antibacterial activity of zinc complexes against Gram-positive and Gram-negative bacterial strains.

  10. Molecular recognition of organic ammonium ions in solution using synthetic receptors

    Directory of Open Access Journals (Sweden)

    Andreas Späth

    2010-04-01

    Full Text Available Ammonium ions are ubiquitous in chemistry and molecular biology. Considerable efforts have been undertaken to develop synthetic receptors for their selective molecular recognition. The type of host compounds for organic ammonium ion binding span a wide range from crown ethers to calixarenes to metal complexes. Typical intermolecular interactions are hydrogen bonds, electrostatic and cation–π interactions, hydrophobic interactions or reversible covalent bond formation. In this review we discuss the different classes of synthetic receptors for organic ammonium ion recognition and illustrate the scope and limitations of each class with selected examples from the recent literature. The molecular recognition of ammonium ions in amino acids is included and the enantioselective binding of chiral ammonium ions by synthetic receptors is also covered. In our conclusion we compare the strengths and weaknesses of the different types of ammonium ion receptors which may help to select the best approach for specific applications.

  11. The effect of the ammonium ion on activated-sludge settling properties

    DEFF Research Database (Denmark)

    Novak, John Thomas

    2001-01-01

    High levels of sodium in wastewater have been found to be detrimental to activated-sludge. settling and dewatering. Another potentially troublesome monovalent cation in activated-sludge systems is the ammonium ion. This study was conducted to determine if the ammonium ion could alter activated...... that the ammonium concentration would increase or by adding sodium. These studies showed that an increase in either sodium or ammonium would cause activated-sludge settling properties to deteriorate. When the monovalent-to-divalent cation ratio on a charge-equivalent basis was increased from 2.4 to 4.7 either...... by addition of sodium or ammonium, the interfacial settling velocity decreased, although the greatest drop was in the reactor containing ammonium. When addition of the nitrification inhibitor was stopped, rapid recovery of nitrification occurred but the settling properties improved more slowly. It seemed...

  12. Amines and ammonium compounds. CXCVIII. Reaction of ammonium salts containing a 2-alkynyl group with bromine and iodine

    Energy Technology Data Exchange (ETDEWEB)

    Gyul' nazaryan, A.K.; Khachatryan, N.G.; Saakyan, T.A.; Kinoyan, F.S.; Panosyan, G.A.; Babayan, A.T.

    1988-08-10

    The reactions of monoammonium, 1,4-and 1,5-bistertiaryammonium, and bisquaternary ammonium salts containing a 2-alkynyl group with bromine and iodine were studied. It was shown that these salts form molecular complexes with iodine and that addition of iodine at the triple bond does not occur. In reaction with bromine in all cases except 1,4-bistrimethylammonio-2-butyne dihalides one molecule of the halogen adds at the triple bond with the formation of salts containing the 2,3-dibromo-2-alkenyl group, which then form a 1:1 complex with bromine.

  13. Ober Phaseniibergange von Ammonium-Alkali-Jodiden und verwandten Halogeniden / Phase Transitions of Ammonium-alkali Iodides and Related Halides

    Science.gov (United States)

    Brauer, Peter

    1981-03-01

    The investigation of the order-disorder transitions of the ammonium-chlorides and -bromides, in which some of the NH4+ are replaced by Cs+, Rb+ or K+, is extended to the corresponding iodides using birefringence and differential thermal analysis. As the temperature range of the martensitic transition (Pm 3 m↔Fm 3 m) is now overlapping the temperature range of the orderdisorder transitions, the former must be included in the measurements. The results allowing an overlook are discussed using the work of Garland, Lushington, and Leung [5

  14. Shock Initiation and Equation of State of Ammonium Nitrate

    Science.gov (United States)

    Robbins, David; Sheffield, Steve; Dattelbaum, Dana; Chellappa, Raja; Velisavljevic, Nenad

    2013-06-01

    Ammonium nitrate (AN) is a widely used fertilizer and mining explosive commonly found in ammonium nitrate-fuel oil. Neat AN is a non-ideal explosive with measured detonation velocities approaching 4 km/s. Previously, we reported a thermodynamically-complete equation of state for AN based on its maximum density, and showed that near-full density AN did not initiate when subjected to shock input conditions up to 22 GPa. In this work, we extend these initial results, by presenting new Hugoniot data for intermediate density neat AN obtained from gas gun-driven plate impact experiments. AN at densities from 1.8 to 1.5 g/cm3 were impacted into LiF windows using a two-stage light gas gun. Dual VISARs were used to measure the interfacial particle velocity wave profile as a function of time following impact. The new Hugoniot data, in addition to updates to thermodynamic parameters derived from structural analysis and vibrational spectroscopy measurements in high pressure diamond anvil cell experiments, are used to refine the unreacted EOS for AN. Furthermore, shock initiation of neat AN was observed as the initial porosity increased (density decreased). Insights into the relationship(s) between initial density and shock initiation sensitivity are also presented, from evidence of shock initiation in the particle velocity profiles obtained for the lower density AN samples.

  15. Ammonium nitrate as an oxidizer in solid composite propellants

    Science.gov (United States)

    Manelis, G. B.; Lempert, D. B.

    2009-09-01

    Despite the fact that ammonium nitrate (AN) has the highest hydrogen content and fairly high oxygen balance (compared to other oxidizers), its extremely low formation enthalpy and relatively low density makes it one of the worst power oxidizers in solid composite propellants (SCP). Nevertheless, AN has certain advantages - the combustion of the compositions containing AN is virtually safe, its combustion products are ecologically clean, it is very accessible and cheap, and also very thermostable (far more stable than ammonium dinitramide (ADN)). Besides, its low density stops being a disadvantage if the propellant has to be used in deep space and therefore, must be carried there with other rocket carriers. The low cost of AN may also become a serious advantage in the AN application even in lower stages of multistage space launchers as well as in one-stage space launchers with low mass fraction of the propellant. The main specific features relevant to the creation of AN-based SCPs with the optimal energetic characteristics are discussed. The use of metals and their hydrides and proper fuel-binders as well as the recent successes in phase stabilization of AN are described.

  16. 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.

  17. Influence of different ammonium, lactate and glutamine concentrations on CCO cell growth

    OpenAIRE

    Slivac, Igor; Blajić, Višnja; Radošević, Kristina; Kniewald, Zlatko; Gaurina Srček, Višnja

    2010-01-01

    In this study the effects of ammonium and lactate on a culture of channel catfish ovary (CCO) cells were examined. We also made investigation on the influence of glutamine, since our previous research revealed that this amino acid stimulated CCO cell growth more than glucose in a concentration-dependent manner. The effect of ammonium in cell culture included the considerable decrease in cell growth rate with eventual growth arrest as well as the retardation of glucose consumption. At ammonium...

  18. Ammonium removal from municipal wastewater with application of ion exchange and partial nitritation/Anammox process

    OpenAIRE

    Malovanyy, Andriy

    2014-01-01

    Nitrogen removal from municipal wastewater with application of Anammox process offers cost reduction, especially if it is combined with maximal use of organic content of wastewater for biogas production. In this study a new technology is proposed, which is based on ammonium concentration from municipal wastewater by ion exchange followed by biological removal of ammonium from the concentrated stream by partial nitritation/Anammox process. In experiments on ammonium concentration four the most...

  19. Influence of Ammonium Salts and Cane Molasses on Growth of Alcaligenes eutrophus and Production of Polyhydroxybutyrate

    OpenAIRE

    Beaulieu, M.; Beaulieu, Y.; Melinard, J.; Pandian, S.; GOULET, J.

    1995-01-01

    The production of polyhydroxybutyrate (PHB) by Alcaligenes eutrophus DSM 545 was studied in a synthetic medium with 3% glucose at pH 7.0 supplemented with several ammonium substrates and cane molasses. Growth was measured by dry cell weight, and the PHB content was measured by gas chromatography. The effects of ammonium sources such as sulfate, nitrate, phosphate, and chloride salts and those of different ammonium sulfate concentrations were evaluated. The best growth and PHB production were ...

  20. Studies on Biquaternary Ammonium Salt Algaecide for Removing Red Tide Algae

    Institute of Scientific and Technical Information of China (English)

    刘洁生; 张珩; 杨维东; 高洁; 柯琼

    2004-01-01

    The paper deals with the removal and control of red tide algae, Phaeoecystis globosa and Alexandrium tamarense by biquaternary ammonium salt algaecide. The results show that the efficient concentration of biquaternary ammonium salt to control the two algaes in 96 h is 0.8 mg · L-1 and 0.4 mg · L-1, respectively. It is found that biquaternary ammonium salt has high efficiency and longer duration of action in the removal and control of algae.Biquaternary ammonium salt might be an excellent algaecide to control HAB.

  1. Highly efficient hydrogen storage system based on ammonium bicarbonate/formate redox equilibrium over palladium nanocatalysts.

    Science.gov (United States)

    Su, Ji; Yang, Lisha; Lu, Mi; Lin, Hongfei

    2015-03-01

    A highly efficient, reversible hydrogen storage-evolution process has been developed based on the ammonium bicarbonate/formate redox equilibrium over the same carbon-supported palladium nanocatalyst. This heterogeneously catalyzed hydrogen storage system is comparable to the counterpart homogeneous systems and has shown fast reaction kinetics of both the hydrogenation of ammonium bicarbonate and the dehydrogenation of ammonium formate under mild operating conditions. By adjusting temperature and pressure, the extent of hydrogen storage and evolution can be well controlled in the same catalytic system. Moreover, the hydrogen storage system based on aqueous-phase ammonium formate is advantageous owing to its high volumetric energy density.

  2. Ammonium sulphate on maize crops under no tillage

    Directory of Open Access Journals (Sweden)

    Maria Anita Gonçalves da Silva

    2012-01-01

    Full Text Available The objectives of this work were to evaluate the management of N and S (as ammonium sulphate fertilization under no-tillage system on the components of maize productivity and on N and S accumulation in the crop, as well as to evaluate the minimum value of the Nitrogen Sufficiency Index (NSI 0.95 as an indicator for side dressing requirements. The experiment had a completely randomized block design with six treatments and four replications carried out in Red Latosol dystrophic soil (Hapludox, in Campo Mourão, Paraná State, where the following treatments in summer growth maize were applied: T1- 120 kg ha-1 N in seeding; T2- 120 kg ha-1 N in side dressing; T3- 40 kg ha-1 N in seeding and 80 kg ha-1 N in side dressing; T4- 30 kg ha-1 N in seeding and 90 kg ha-1 N in side dressing, monitored by a chlorophyll meter using the Nitrogen Sufficiency Index (NSI; T5- 120 kg ha-1 N anticipated in wheat seeding; T6- without nitrogen fertilization. NSI was determined by the relationship between the leaf chlorophyll index (ICF average of T4 plants and that one in the plot fertilized with 120 kg ha-1 N at the maize seed sowing (T1. During two years, ammonium sulphate was applied to the maize crop after wheat under no tillage system. In the first year, with adequate rainfall, the maize yield was similar to the one in which the complete ammonium sulphate dose application was done in maize seeding and side dressing. The anticipated fertilization to wheat seed sowing resulted in maize yield without difference from the parceled form. In the second year, with irregular rainfall, all treatments with N were similar and they increased maize yield compared to that without N fertilization. NSI of 0.95 was not efficient to evaluate maize N requirements in side dressing, and resulted in lower maize yield. N was accumulated mainly in the grains unlike S that accumulated in the plant shoots; both were highly correlated to maize productivity.

  3. Single stage biological nitrogen removal by nitritation and anaerobic ammonium oxidation in biofilm systems.

    Science.gov (United States)

    Helmer, C; Tromm, C; Hippen, A; Rosenwinkel, K H; Seyfried, C F; Kunst, S

    2001-01-01

    In full scale wastewater treatment plants with at times considerable deficits in the nitrogen balances, it could hitherto not be sufficiently explained which reactions are the cause of the nitrogen losses and which micro-organisms participate in the process. The single stage conversion of ammonium into gaseous end-products--which is henceforth referred to as deammonification--occurs particularly frequently in biofilm systems. In the meantime, one has succeeded to establish the deammonification processes in a continuous flow moving-bed pilot plant. In batch tests with the biofilm covered carriers, it was possible for the first time to examine the nitrogen conversion at the intact biofilm. Depending on the dissolved oxygen (DO) concentration, two autotrophic nitrogen converting reactions in the biofilm could be proven: one nitritation process under aerobic conditions and one anaerobic ammonium oxidation. With the anaerobic ammonium oxidation, ammonium as electron donor was converted with nitrite as electron acceptor. The end-product of this reaction was N2. Ammonium and nitrite did react in a stoichiometrical ratio of 1:1.37, a ratio which has in the very same dimension been described for the ANAMMOX-process (1:1.31 +/- 0.06). Via the oxygen concentration in the surrounding medium, it was possible to control the ratio of nitritation and anaerobic ammonium oxidation in the nitrogen conversion of the biofilm. Both processes were evenly balanced at a DO concentration of 0.7 mg/l, so that it was possible to achieve a direct, almost complete elimination of ammonium without addition of nitrite. One part of the provided ammonium did participate in the nitritation, the other in the anaerobic ammonium oxidation. Through the aerobic ammonium oxidation into nitrite within the outer oxygen supplied layers of the biofilm, the reaction partner was produced for the anaerobic ammonium oxidation within the inner layers of the biofilm. PMID:11379106

  4. Studies on a Cationically Modified Quaternary Ammonium Salt of Lignin

    Institute of Scientific and Technical Information of China (English)

    YANG Ai-li; JIANG Wen-ju

    2007-01-01

    A new quaternary ammonium salt monomer was synthesized and a quaternary amination of lignin( noted as QL),with the monomer was carried out by grafting copolymerization. The products were characterized by Fourier Transform Infrared spectroscopy(FTIR). The experimental results indicate that the yield of the monomer was 99.06%, and the conversion of the monomer and the grafting yield of QL were 93.69% and 185.78%, respectively. The feasibility of QL as the fiocculant to be applied in color removal of five artificial dyes, eriochrome black T( dye A), gongo red( dye B), direct fast black G (dye C), cuprofix blue green B (dye D), and acid black ATT (dye E) was examined.Results show that QL exhibits the favorable flocculation performance and high stability.

  5. Crystal structure of tris-(hydroxyl-ammonium) orthophosphate.

    Science.gov (United States)

    Leinemann, Malte; Jess, Inke; Boeckmann, Jan; Näther, Christian

    2015-11-01

    The crystal structure of the title salt, ([H3NOH](+))3·[PO4](3-), consists of discrete hydroxyl-ammonium cations and ortho-phos-phate anions. The atoms of the cation occupy general positions, whereas the anion is located on a threefold rotation axis that runs through the phospho-rus atom and one of the phosphate O atoms. In the crystal structure, cations and anions are linked by inter-molecular O-H⋯O and N-H⋯O hydrogen bonds into a three-dimensional network. Altogether, one very strong O-H⋯O, two N-H⋯O hydrogen bonds of medium strength and two weaker bifurcated N-H⋯O inter-actions are observed. PMID:26594525

  6. 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.

  7. Polishing of quartz by rapid etching in ammonium bifluoride.

    Science.gov (United States)

    Vallin, Orjan; Danielsson, Rolf; Lindberg, Ulf; Thornell, Greger

    2007-07-01

    The etch rate and surface roughness of polished and lapped AT-cut quartz subjected to hot (90, 110, and 130 degrees C), concentrated (50, 65, 80 wt %) ammonium bi-fluoride have been investigated. Having used principal component analysis to verify experimental solidity and analyze data, we claim with confidence that this parameter space does not, as elsewhere stated, allow for a polishing effect or even a preserving setting. Etch rates were found to correlate well, and possibly logarithmically, with temperature except for the hottest etching applied to lapped material. Roughness as a function of temperature and concentration behaved well for the lapped material, but lacked systematic variation in the case of the polished material. At the lowest temperature, concentration had no effect on etch rate or roughness. Future efforts are targeted at temperatures and concentrations closer to the solubility limit.

  8. Ammonium derivatives of chromenones and quinolinones as lead antimicrobial agents

    Indian Academy of Sciences (India)

    Shilpi Gupta; Seema Singh; Abha Kathuria; Manish Kumar; Sweta Sharma; Ram Kumar; Virinder S Parmar; Bharat Singh; Anjali Gupta; Erik Van Der Eycken; Gainda L Sharma; Sunil K Sharma

    2012-03-01

    A series of novel ammonium derivatives were synthesized and examined for their antimicrobial efficacy. Comparison of antimicrobial spectrum revealed that compounds 9, 11, 16 and 23 had strong potential against pathogens in vitro. Cytotoxicity results showed compound 9 to be least toxic, it is non-toxic to A549 and U87 cells in MTT assay and exhibits marginal toxicity (15-20%) to human erythrocytes at a concentration of 1000 g/ml as compared to 100% lysis of cells by 31.25 g/ml of the standard drug amphotericin B. This compound has MIC values in the range of 1.95-31.25 g/disc in DDA against different pathogens and may considered to be an important lead antimicrobial molecule for further exploration.

  9. A facile synthesis of ω-aminoalkyl ammonium hydrogen phosphates

    Institute of Scientific and Technical Information of China (English)

    Wei Bo Kong; Xiao Yong Zhou; Yang Yang; Xing Yi Xie

    2012-01-01

    A series of ω-aminoalkyl ammonium hydrogen phosphates were synthesized through a simple and efficient three-step method.The starting materials,ω-aminoalkyl alcohols (AC-n,with carbon number n =3,4,5,6),were amino-protected with 9-fluorenylmethyl chloroformate (Fmoc-Cl),followed by phosphorylation with POCl3 and deprotection in piperidine/DMF The structures of each intermediate and final product were confirmed by 1H NMR,FTIR and mass spectrum.The yield of each step was about 77-92%,with a total yield higher than 56%.This new method was superior in low-cost raw materials,mild reaction temperatures (0-25 ℃) and easy purification methods.

  10. Hibiscus sabdariffa Affects Ammonium Chloride-Induced Hyperammonemic Rats

    Directory of Open Access Journals (Sweden)

    M. Mohamed Essa

    2007-01-01

    Full Text Available Hibiscus sabdariffa (HS is an edible medicinal plant, indigenous to India, China and Thailand and is used in Ayurveda and traditional medicine. Alcoholic extract of HS leaves (HSEt was studied for its anti-hyperammonemic and antioxidant effects in brain tissues of ammonium chloride-induced hyperammonemic rats. Oral administration of HSEt (250 mg kg−1 body weight significantly normalizes the levels of ammonia, urea, uric acid, creatinine and non-protein nitrogen in the blood. HSEt significantly reduced brain levels of lipid peroxidation products such as thiobarbituric acid and reactive substances (TBARS and hydroperoxides (HP. However, the administered extract significantly increased the levels of antioxidants such as catalase (CAT, superoxide dismutase (SOD, glutathione peroxidase (GPx and reduced glutathione (GSH in brain tissues of hyperammonemic rats. This investigation demonstrates significant anti-hyperammonemic and antioxidant activity of HS.

  11. 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.

  12. 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.

  13. Cold Case: Radar investigation of ammonium sulfate cryovolcanism on Titan

    Science.gov (United States)

    Thomann, C.; Hayes, A. G.; Hofgartner, J.; Lunine, J. I.; Le Gall, A.

    2012-12-01

    The detection of a large tidal k2 value from Cassini [1] constitutes very strong evi-dence for a subcrustal ocean, most plausibly dominated by water. However, the secondary constituents are not known. One interesting possibility that has received scant attention in analysis of surface data sets is that the ocean contain aqueous ammonium sulfates, which erupted on the surface in the past to create vast, smooth plains [2]. We adopt the hypothesis that the undifferentiated plains—the "bland-lands" in the mid-latitudes of Titan—are these deposits, and test it using radiometry with SAR data. Lopez et al (this conference) investigate the global distribution and possible origin of this type of unit. We extracted SAR and radiometry-during-SAR data sets from the PDS, and pro-duced maps of brightness temperatures. The SAR imagery was used to identify locations where crossovers exist -some of which are in the undifferentiated plains--and hence where brightness temperatures at different incidence angles are available. We derived emissivities from the data using a simple radiometric model [3] to ac-count for the brightness temperature differences as a function of surface roughness, volume scattering and emissivity. We test the hypothesis by assessing whether the derived emissivities and volume scattering in the bland-lands are consistent with the model cryoclastic ash of ice and ammonium sulfate proposed in [2], distinct from that in other terrains. [1] L. Iess, R.A. Jacobson, M. Ducci, D.J. Stevenson, J.I. Lunine, J.W. Armstrong, S.W. Asmar, P. Racioppa, N.J. Rappaport, P. Tortora, Science, 337, 457 (2012). [2] A.D. Fortes, P.M. Grinrod, S.K. Trickett, L. Vocadlo. Icarus, 188, 139 (2007). [3] T.L. White and J.R. Cogdell. The Moon, 6, 235 (1973).

  14. Syntheses and Crystal Structures of Two Two-dimensional Coordination Polymers with 2,3-Dimethylpyrazine-1,4-dioxide and Thiocyanate as Mixed Bridge Ligands

    Institute of Scientific and Technical Information of China (English)

    SHI Jing-Min; LI Wei-Nan; ZHANG Feng-Xia; ZHANG Xia; LIU Lian-Dong

    2007-01-01

    Two two-dimensional coordination polymers,[Cd(μ1,3-SCN-)2(μ1,6-L)]n 1 and [Co(μ1,3-SCN-)2(μ1,6-L)]n 2,have been synthesized with 2,3-dimethylpyrazine-1,4-dioxide (L) and thiocyanate as mixed bridging ligands,and their crystal structures were determined by X-ray crystallography.Both crystals belong to monoclinic system,space group C2/c.The other crystal parameters are as follows:for complex 1:a = 9.732(3),b = 14.658(5),c = 8.811(3) (A),β =102.935(4)°,Z = 4,V = 1225.1(7)(A)3,CsHsCdN4O2S2,Mr = 368.71,Dc.-- 1.999 g/cm3,F(000) =720 andμ = 2.117 mm-1;for complex 2:a = 9.528(7),b = 14.563(11),c = 8.415(6) (A),β =102.195(9)°,V= 1141.3(14) (A)3,Z = 4,C8H8CoN4O2S2,Mr = 315.23,Dc = 1.835 g/cm3,F(000) =636 andμ = 1.863 mm-1.The two complexes show similar two-dimensional sheet structures.Along the c axis one-dimensional chains are constructed by the coordination of Cd(Ⅱ) (or Co(Ⅱ))ions with μ1,6-L bridging ligand,and the μ1,3-SCN- bridging ligands make the chains connect to each other,resulting in the formation of a two-dimensional sheet on the ac plane.

  15. IC Determination of Thiocyanate in Liquid Dairy Products%离子色谱法测定液体乳制品中硫氰酸盐

    Institute of Scientific and Technical Information of China (English)

    张宝; 刘晓玲; 李东刚; 孙长华

    2011-01-01

    提出了离子色谱法测定液体乳中硫氰酸盐的方法.鲜奶或酸奶样品经乙腈提取和C18固相萃取柱净化后,再经Ion Pac AG11-HG保护柱及Dionex ICS-3000分离柱分离,由70 mmol·L-1氢氧化钾溶液洗脱,利用电导检测器检测.硫氰酸盐的质量浓度在0.20~10.0 mg·L-1范围内呈线性,方法的检出限(3S/N)为0.08 mg·L-1.方法用于鲜奶和酸奶样品分析,回收率在92.5%~104.5%之间,相对标准偏差(n=6)小于4.5%.%Ion chromatography was applied to the determination of thiocyanate in liquid dairy product.The samples of fresh milk or sour milk were extracted with acetonitrile and purified on C18 SPE column.The protective column (Ion Pac AGll-HG) and separation column (Dionex ICS-3000) were used for separation, with 70 mmol·L-1 KOH solution as mobile phase, and conductivity detector was used in the determination.Linearity range was found between 0.20-10.0 mg·L-1, and detection limit (3S/N) was found to be 0.08 mg· L-1.The proposed method was applied to the analysis of fresh milk and sour milk, giving values of recovery in the range of 92.5%-104.5% with RSD's (n=6)less than 4.5%.

  16. Excreted thiocyanate detects live reef fishes illegally collected using cyanide--a non-invasive and non-destructive testing approach.

    Directory of Open Access Journals (Sweden)

    Marcela C M Vaz

    Full Text Available Cyanide fishing is a method employed to capture marine fish alive on coral reefs. They are shipped to markets for human consumption in Southeast Asia, as well as to supply the marine aquarium trade worldwide. Although several techniques can be used to detect cyanide in reef fish, there is still no testing method that can be used to survey the whole supply chain. Most methods for cyanide detection are time-consuming and require the sacrifice of the sampled fish. Thiocyanate anion (SCN(- is a metabolite produced by the main metabolic pathway for cyanide anion (CN(- detoxification. Our study employed an optical fiber (OF methodology (analytical time 3.16 µg L(-1 of SCN(- in seawater. Given that marine fish exposed to cyanide excrete SCN(- in the urine, elevated levels of SCN(- present in the seawater holding live reef fish indicate that the surveyed specimens were likely exposed to cyanide. In our study, captive-bred clownfish (Amphiprion clarkii pulse exposed for 60 s to either 12.5 or 25 mg L(-1 of CN(- excreted up to 6.96±0.03 and 9.84±0.03 µg L(-1 of SCN(-, respectively, during the 28 days following exposure. No detectable levels of SCN(- were recorded in the water holding control organisms not exposed to CN(-, or in synthetic seawater lacking fish. While further research is necessary, our methodology can allow a rapid detection of SCN(- in the holding water and can be used as a screening tool to indicate if live reef fish were collected with cyanide.

  17. Structural evidence of substrate specificity in mammalian peroxidases: structure of the thiocyanate complex with lactoperoxidase and its interactions at 2.4 A resolution.

    Science.gov (United States)

    Sheikh, Ishfaq Ahmed; Singh, Amit Kumar; Singh, Nagendra; Sinha, Mau; Singh, S Baskar; Bhushan, Asha; Kaur, Punit; Srinivasan, Alagiri; Sharma, Sujata; Singh, Tej P

    2009-05-29

    The crystal structure of the complex of lactoperoxidase (LPO) with its physiological substrate thiocyanate (SCN(-)) has been determined at 2.4A resolution. It revealed that the SCN(-) ion is bound to LPO in the distal heme cavity. The observed orientation of the SCN(-) ion shows that the sulfur atom is closer to the heme iron than the nitrogen atom. The nitrogen atom of SCN(-) forms a hydrogen bond with a water (Wat) molecule at position 6'. This water molecule is stabilized by two hydrogen bonds with Gln(423) N(epsilon2) and Phe(422) oxygen. In contrast, the placement of the SCN(-) ion in the structure of myeloperoxidase (MPO) occurs with an opposite orientation, in which the nitrogen atom is closer to the heme iron than the sulfur atom. The site corresponding to the positions of Gln(423), Phe(422) oxygen, and Wat(6)' in LPO is occupied primarily by the side chain of Phe(407) in MPO due to an entirely different conformation of the loop corresponding to the segment Arg(418)-Phe(431) of LPO. This arrangement in MPO does not favor a similar orientation of the SCN(-) ion. The orientation of the catalytic product OSCN(-) as reported in the structure of LPO.OSCN(-) is similar to the orientation of SCN(-) in the structure of LPO.SCN(-). Similarly, in the structure of LPO.SCN(-).CN(-), in which CN(-) binds at Wat(1), the position and orientation of the SCN(-) ion are also identical to that observed in the structure of LPO.SCN.

  18. Clinoptilolite-based mixed matrix membranes for the selective recovery of potassium and ammonium

    NARCIS (Netherlands)

    Casadella, A.; Kuntke, P.; Schaetzle, O.; Loos, K.

    2016-01-01

    . A clinoptilolite-based mixed matrix membrane (MMM) was developed and studied for the selective recovery of ammonium and potassium. Adsorption of sodium (Na+), potassium (K+) and ammonium (NH4+) was investigated with single salt and equimolar salt solution under static and dynamic conditions. Furth

  19. 75 FR 56489 - Separation Distances of Ammonium Nitrate and Blasting Agents From Explosives or Blasting Agents...

    Science.gov (United States)

    2010-09-16

    ... definition of ammonium nitrate fertilizer issued by the Fertilizer Institute'' in its ``Definition and Test Procedures for Ammonium Nitrate Fertilizer.'' The Fertilizer Institute (TFI) ] is a voluntary, non-profit trade association of the fertilizer industry that currently has more than 175 members. See...

  20. 76 FR 23569 - Termination of the Suspension Agreement on Solid Fertilizer Grade Ammonium Nitrate From the...

    Science.gov (United States)

    2011-04-27

    ... Antidumping Duty Investigation: Solid Fertilizer Grade Ammonium Nitrate from the Russian Federation, 64 FR... Less Than Fair Value: Solid Fertilizer Grade Ammonium Nitrate from the Russian Federation, 65 FR 1139... International Trade Administration Termination of the Suspension Agreement on Solid Fertilizer Grade...

  1. Photo-Fenton-like degradation of azo dye methyl orange using synthetic ammonium and hydronium jarosite

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Zhihui [Department of Chemistry, College of Science, Nanjing Agricultural University, Nanjing 210095 (China); Liang, Jianru [Department of Environmental Engineering, College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095 (China); Zhou, Lixiang, E-mail: lxzhou@njau.edu.cn [Department of Environmental Engineering, College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095 (China)

    2013-01-05

    Highlights: Black-Right-Pointing-Pointer Hydronium and ammonium jarosite could catalyze the oxidation of methyl orange in photo-Fenton-like process. Black-Right-Pointing-Pointer The oxidation process is essentially heterogeneous, not homogeneous. Black-Right-Pointing-Pointer Hydronium jarosite has stronger reactivity than ammonium jarosite. - Abstract: Ammonium and hydronium jarosite were prepared by hydrothermal method with urea as the homogeneous precipitant. X-ray diffraction, field-emission scanning electron microscope, X-ray photoelectron spectrum, UV-vis spectra and fourier transform infrared spectrum were used to characterize the resulting products. The photodegradation efficiency of the prepared ammonium and hydronium jarosite was studied in a photo-Fenton-like process using methyl orange (MO) as target pollutant. The photocatalytic degradation of MO over synthetic ammonium and hydronium jarosite under various conditions, such as catalysts loading, H{sub 2}O{sub 2} concentration and initial pH, has been investigated. Results show that ammonium and hydronium jarosite have satisfactory photocatalysis effect in degradation of MO azo dye, and that the reactivity of hydronium jarosite toward the mineralization of MO was higher than that of ammonium jarosite. The novel ammonium and hydronium jarosite catalysts would be important for industrial applications due to their high photoactivity, little iron leaching and low cost.

  2. Ammonium across a Selective Polymer Inclusion Membrane : Characterization, Transport, and Selectivity

    NARCIS (Netherlands)

    Casadella, Anna; Schaetzle, Olivier; Loos, Katja

    2016-01-01

    The recovery of ammonium from urine requires distinguishing and excluding sodium and potassium. A polymer inclusion membrane selective for ammonium is developed using an ionophore based on pyrazole substituted benzene. The interactions of the components are studied, as well as their effect on transp

  3. Temperature effects in the absorption spectra and exciton luminescence in ammonium halides

    International Nuclear Information System (INIS)

    Warm-up behavior of the first maximum exciton absorption bands in ammonium halides is explored. Under phase transition occurs offset of bands, bound both with changing a parameter of lattice, and efficient mass of exciton. Warm-up dependency of quantum leaving a luminescence of self-trapped excitons in ammonium halides is measured. (author)

  4. 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 been

  5. Effects of Ammonium and Nitrite on Growth and Competitive Fitness of Cultivated Methanotrophic Bacteria▿

    OpenAIRE

    Nyerges, Györgyi; Han, Suk-Kyun; Stein, Lisa Y.

    2010-01-01

    The effects of nitrite and ammonium on cultivated methanotrophic bacteria were investigated. Methylomicrobium album ATCC 33003 outcompeted Methylocystis sp. strain ATCC 49242 in cultures with high nitrite levels, whereas cultures with high ammonium levels allowed Methylocystis sp. to compete more easily. M. album pure cultures and cocultures consumed nitrite and produced nitrous oxide, suggesting a connection between denitrification and nitrite tolerance.

  6. Ammonium-oxidizing bacteria facilitate aerobic degradation of sulfanilic acid in activated sludge.

    Science.gov (United States)

    Chen, Gang; Ginige, Maneesha P; Kaksonen, Anna H; Cheng, Ka Yu

    2014-01-01

    Sulfanilic acid (SA) is a toxic sulfonated aromatic amine commonly found in anaerobically treated azo dye contaminated effluents. Aerobic acclimatization of SA-degrading mixed microbial culture could lead to co-enrichment of ammonium-oxidizing bacteria (AOB) because of the concomitant release of ammonium from SA oxidation. To what extent the co-enriched AOB would affect SA oxidation at various ammonium concentrations was unclear. Here, a series of batch kinetic experiments were conducted to evaluate the effect of AOB on aerobic SA degradation in an acclimatized activated sludge culture capable of oxidizing SA and ammonium simultaneously. To account for the effect of AOB on SA degradation, allylthiourea was used to inhibit AOB activity in the culture. The results indicated that specific SA degradation rate of the mixed culture was negatively correlated with the initial ammonium concentration (0-93 mM, R²= 0.99). The presence of AOB accelerated SA degradation by reducing the inhibitory effect of ammonium (≥ 10 mM). The Haldane substrate inhibition model was used to correlate substrate concentration (SA and ammonium) and oxygen uptake rate. This study revealed, for the first time, that AOB could facilitate SA degradation at high concentration of ammonium (≥ 10 mM) in an enriched activated sludge culture.

  7. Suppression of interference in the AAS determination of chromium by use of ammonium bifluoride.

    Science.gov (United States)

    Purushottam, A; Naidu, P P; Lal, S S

    1973-07-01

    Addition of 1% of ammonium bifluoride successfully suppresses interference by diverse ions in the atomic-absorption determination of chromium(VI). If the sample solutions also contain chromium(III) addition of 1% of ammonium bifluoride and 0.2% of sodium sulphate is recommended for the suppression.

  8. Irritant contact dermatitis due to ammonium bifluoride in two infant twins.

    Science.gov (United States)

    Toledo, Fernando; Silvestre, Juan Francisco; Cuesta, Laura; Bañuls, José

    2013-01-01

    Ammonium bifluoride is one of the most corrosive acids that may produce severe chemical burns when in contact with skin. This hazardous chemical is widely used in household products. We report two pediatric cases of irritant contact dermatitis after exposure to a rust remover, which contained ammonium bifluoride.

  9. Effect of quaternary ammonium salts on flotation behavior of aluminosilicate minerals

    Institute of Scientific and Technical Information of China (English)

    ZHAO Sheng-gui; ZHONG Hong; LIU Guang-yi

    2007-01-01

    The electrokinetic properties and flotation of diaspore, kaolinite, pyrophyllite and illite with quaternary ammonium salts collectors were studied. The results of flotation tests show that the collecting ability of quaternary ammonium salts for the four minerals is in the order(from strong to weak) of octadecyl dimethyl benzyl ammonium chloride(ODBA), cetyl trimethyl ammonium bromide(CTAB), dodecyl trimethyl ammonium chloride(DTAC). Under the condition of alkalescence, it is possible to separate the diaspore from the silicate minerals such as kaolinite, illite and pyrophyllite using quaternary ammonium salts as collector. Isoelectric points (IEP) of diaspore, kaolinite, pyrophyllite and illite are pH=6.0, 3.4, 2.3 and 3.2, respectively. Quaternary ammonium salts can change ζ-potential of the aluminosilicate minerals obviously. The flotation mechanisms were explained by ζ-potential and Fourier transform infrared spectrum (FT-IR) measurements. The results demonstrate that only electrostatic interaction takes place between aluminosilicate minerals (diaspore, kaolinite, pyrophyllite and illite) and quaternary ammonium salts.

  10. Ammonium addition inhibits 13C-methane incorporation into methanotroph membrane lipids in a freshwater sediment

    NARCIS (Netherlands)

    Nold, S.C.; Boschker, H.T.S.; Pel, R.; Laanbroek, H.J.

    1999-01-01

    To investigate the effect of ammonium addition on the species composition and activity of freshwater methane oxidizing bacteria, intact sediment cores were labeled with 13CH4 and incubated under ambient and elevated ammonium concentrations. After 7 days, methanotroph activity was assessed by quantif

  11. 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 (f

  12. Novel carbohydrate-based chiral ammonium ionic liquids derived from isomannide

    DEFF Research Database (Denmark)

    Kumar, Vineet; Pei, Cao; Olsen, Carl E.;

    2008-01-01

    This report describes the synthesis and characterization of novel carbohydrate-based chiral ammonium ionic liquids using isomannide as a biorenewable substrate. The diastereomeric interactions of these chiral ammonium ionic liquids with racemic Mosher's acid salt have been studied using NMR, which...

  13. Nitrogen phosphoric fertilizer production technology on the base of Central Kyzylkum phosphorites and ammonium nitrate melt

    OpenAIRE

    Shavkat Namazov; Akhmed Reymov; Nazarkul Pirmanov; Rashid Kurbaniyazov

    2012-01-01

    The process of obtaining nitrogen phosphoric fertilizer by introduction Central Kyzylkum phosphates and ammonium nitrate melt is studied. On the base of these results production technology diagram for nitrogen phosphoric fertilizer is offered. The given technology was approved and developed at the functioning devices of OJSC “NAVOIAZOT” ammonium nitrate shop.

  14. Nitrogen phosphoric fertilizer production technology on the base of Central Kyzylkum phosphorites and ammonium nitrate melt

    Directory of Open Access Journals (Sweden)

    Shavkat Namazov

    2012-11-01

    Full Text Available The process of obtaining nitrogen phosphoric fertilizer by introduction Central Kyzylkum phosphates and ammonium nitrate melt is studied. On the base of these results production technology diagram for nitrogen phosphoric fertilizer is offered. The given technology was approved and developed at the functioning devices of OJSC “NAVOIAZOT” ammonium nitrate shop.

  15. Nitrogen removal by autotrophic ammonium oxidizing bacteria enrichment under anaerobic conditions

    Directory of Open Access Journals (Sweden)

    Pongsak (Lek Noophan

    2008-07-01

    Full Text Available Sludge from an anoxic tank at the centralized wastewater treatment plant, Nong Khaem, Bangkok, Thailand, was inoculatedin an anaerobic sequencing batch reactor (ASBR. The optimal compositions and operating conditions of the stock of autotrophic ammonium oxidizing bacteria medium were determined. The process of oxidizing ammonium with bacteria under anaerobic conditions is often referred to as the Anammox process (NO2- to N2 gas, using NH4+ as the electron donor and NO2- as the electron acceptor. The startup period for the anammox culture took more than three months. With ammoniumand nitrite concentration ratios of 1:1.38 and 1:1.6, the nitrogen conversion rate zero order. Fluorescent in situ hybridization(FISH was used to identify specific autotrophic ammonium oxidizing bacteria (Nitrosomonas spp., Candidatus Brocadia anammoxidans, and Candidatus Kuenenia stuttgartiensis. Results from this work demonstrated a shift in the species of ammonium oxidizing bacteria from Nitrosomonas spp. to Candidati Brocadia anammoxidans and Kuenenia stuttgartiensis, with increased ammonium concentrations from 3 mM to 15 mM. Under NH4+:NO2- ratios of 1:1.38 and 1:1.6 the ammoniumoxidizing bacteria were able to remove both ammonium and nitrite simultaneously. The specific nitrogen removal rate of theanammox bacteria (Candidati Brocadia anammoxidans and Kuenenia stuttgartiensis was significantly higher than that of anaerobic ammonium oxidizing bacteria (Nitrosomonas spp.. Anaerobic ammonium oxidizing bacteria (Candidati Brocadia anammoxidans and Kuenenia stuttgartiensis are strict anaerobes.

  16. Alkali metal and ammonium chlorides in water and heavy water (binary systems)

    CERN Document Server

    Cohen-Adad, R

    1991-01-01

    This volume surveys the data available in the literature for solid-fluid solubility equilibria plus selected solid-liquid-vapour equilibria, for binary systems containing alkali and ammonium chlorides in water or heavy water. Solubilities covered are lithium chloride, sodium chloride, potassium chloride, rubidium chloride, caesium chloride and ammonium chloride in water and heavy water.

  17. 77 FR 21527 - Ammonium Nitrate From Russia: Correction to Notice of Opportunity To Request Administrative Review

    Science.gov (United States)

    2012-04-10

    ...; Opportunity To Request Administrative Review, 77 FR 63 (April 2, 2012). This notice serves as a correction to... International Trade Administration Ammonium Nitrate From Russia: Correction to Notice of Opportunity To Request... of the antidumping duty orders and inadvertently omitted Ammonium Nitrate from Russia, POR...

  18. Removal of ammonium ions from wastewater: A short review in development of efficient methods

    Directory of Open Access Journals (Sweden)

    V.K. Gupta

    2015-04-01

    Full Text Available Ammonium ions wastewater pollution has become one of the most serious environmental problems today. The treatment of ammonium ions is a special concern due to their recalcitrance and persistence in the environment. In recent years, various methods for ammonium ion removal from wastewater have been extensively studied. This paper reviews the current methods that have been used to treat ammonium ion wastewater and evaluates these techniques. These technologies include ion exchange, adsorption, biosorption, wet air oxidation, biofiltration, diffused aeration, nitrification and denitrification methods. About 75 published studies (1979-2015 are reviewed in this paper. It is evident from the literature survey articles that ion exchange, adsorption and biological technology are the most frequently studied for the treatment of ammonium ion wastewater.

  19. Kinetics Analysis on Mixing Calcination Process of Fly Ash and Ammonium Sulfate

    Institute of Scientific and Technical Information of China (English)

    Peng Wang; Laishi Li; Dezhou Wei

    2014-01-01

    abstract The further development of the extraction of alumina that is produced in the calcination process of ammonium sulfate mixed with fly ash was limited because of the lack of systematic theoretical study. In order to aggrandize the research of the calcination process, the kinetics and reaction mechanism of the calcinations were studied. The result suggests that there are two stages in the calcination process, and the alumina extraction rate increases swiftly in the initial stage, but slows down increasing in the later stage. The apparent activation energy of the initial and later stages equals to 13.31 and 35.65 kJ·mol-1, respectively. In the initial stage, ammonium sulfate reacts directly with mullite in the fly ash to form ammonium aluminum sulfate, while in the later stage, alumi-num sulfate is formed by the reaction between ammonium aluminum sulfate and ammonium sulfate.

  20. Interaction between Ammonium Toxicity and Green Tide Development Over Seagrass Meadows: A Laboratory Study

    Science.gov (United States)

    Moreno-Marín, Francisco; Vergara, Juan J.; Pérez-Llorens, J. Lucas; Pedersen, Morten F.; Brun, Fernando G.

    2016-01-01

    Eutrophication affects seagrasses negatively by increasing light attenuation through stimulation of biomass of fast-growing, bloom-forming algae and because high concentrations of ammonium in the water can be toxic to higher plants. We hypothesized nevertheless, that moderate amounts of nitrophilic macroalgae that coexists with seagrasses under eutrophic conditions, can alleviate the harmful effects of eutrophication on seagrasses by reducing ammonium concentrations in the seawater to non-toxic levels because such algae have a very large capacity to take up inorganic nutrients. We studied therefore how combinations of different ammonium concentrations (0, 25 and 50 μM) and different standing stocks of macroalgae (i.e. 0, 1 and 6 layers of Ulva sp.) affected survival, growth and net production of the seagrass Zostera noltei. In the absence of Ulva sp., increasing ammonium concentrations had a negative influence on the performance of Z. noltei. The presence of Ulva sp. without ammonium supply had a similar, but slightly smaller, negative effect on seagrass fitness due to light attenuation. When ammonium enrichment was combined with presence of Ulva sp., Ulva sp. ameliorated some of negative effects caused by high ammonium availability although Ulva sp. lowered the availability of light. Benthic microalgae, which increased in biomass during the experiment, seemed to play a similar role as Ulva sp.–they contributed to remove ammonium from the water, and thus, aided to keep the ammonium concentrations experienced by Z. noltei at relatively non-toxic levels. Our findings show that moderate amounts of drift macroalgae, eventually combined with increasing stocks of benthic microalgae, may aid seagrasses to alleviate toxic effects of ammonium under eutrophic conditions, which highlights the importance of high functional diversity for ecosystem resistance to anthropogenic disturbance. PMID:27035662

  1. Interaction between Ammonium Toxicity and Green Tide Development Over Seagrass Meadows: A Laboratory Study.

    Science.gov (United States)

    Moreno-Marín, Francisco; Vergara, Juan J; Pérez-Llorens, J Lucas; Pedersen, Morten F; Brun, Fernando G

    2016-01-01

    Eutrophication affects seagrasses negatively by increasing light attenuation through stimulation of biomass of fast-growing, bloom-forming algae and because high concentrations of ammonium in the water can be toxic to higher plants. We hypothesized nevertheless, that moderate amounts of nitrophilic macroalgae that coexists with seagrasses under eutrophic conditions, can alleviate the harmful effects of eutrophication on seagrasses by reducing ammonium concentrations in the seawater to non-toxic levels because such algae have a very large capacity to take up inorganic nutrients. We studied therefore how combinations of different ammonium concentrations (0, 25 and 50 μM) and different standing stocks of macroalgae (i.e. 0, 1 and 6 layers of Ulva sp.) affected survival, growth and net production of the seagrass Zostera noltei. In the absence of Ulva sp., increasing ammonium concentrations had a negative influence on the performance of Z. noltei. The presence of Ulva sp. without ammonium supply had a similar, but slightly smaller, negative effect on seagrass fitness due to light attenuation. When ammonium enrichment was combined with presence of Ulva sp., Ulva sp. ameliorated some of negative effects caused by high ammonium availability although Ulva sp. lowered the availability of light. Benthic microalgae, which increased in biomass during the experiment, seemed to play a similar role as Ulva sp.--they contributed to remove ammonium from the water, and thus, aided to keep the ammonium concentrations experienced by Z. noltei at relatively non-toxic levels. Our findings show that moderate amounts of drift macroalgae, eventually combined with increasing stocks of benthic microalgae, may aid seagrasses to alleviate toxic effects of ammonium under eutrophic conditions, which highlights the importance of high functional diversity for ecosystem resistance to anthropogenic disturbance. PMID:27035662

  2. Interaction between Ammonium Toxicity and Green Tide Development Over Seagrass Meadows: A Laboratory Study.

    Directory of Open Access Journals (Sweden)

    Francisco Moreno-Marín

    Full Text Available Eutrophication affects seagrasses negatively by increasing light attenuation through stimulation of biomass of fast-growing, bloom-forming algae and because high concentrations of ammonium in the water can be toxic to higher plants. We hypothesized nevertheless, that moderate amounts of nitrophilic macroalgae that coexists with seagrasses under eutrophic conditions, can alleviate the harmful effects of eutrophication on seagrasses by reducing ammonium concentrations in the seawater to non-toxic levels because such algae have a very large capacity to take up inorganic nutrients. We studied therefore how combinations of different ammonium concentrations (0, 25 and 50 μM and different standing stocks of macroalgae (i.e. 0, 1 and 6 layers of Ulva sp. affected survival, growth and net production of the seagrass Zostera noltei. In the absence of Ulva sp., increasing ammonium concentrations had a negative influence on the performance of Z. noltei. The presence of Ulva sp. without ammonium supply had a similar, but slightly smaller, negative effect on seagrass fitness due to light attenuation. When ammonium enrichment was combined with presence of Ulva sp., Ulva sp. ameliorated some of negative effects caused by high ammonium availability although Ulva sp. lowered the availability of light. Benthic microalgae, which increased in biomass during the experiment, seemed to play a similar role as Ulva sp.--they contributed to remove ammonium from the water, and thus, aided to keep the ammonium concentrations experienced by Z. noltei at relatively non-toxic levels. Our findings show that moderate amounts of drift macroalgae, eventually combined with increasing stocks of benthic microalgae, may aid seagrasses to alleviate toxic effects of ammonium under eutrophic conditions, which highlights the importance of high functional diversity for ecosystem resistance to anthropogenic disturbance.

  3. Competition for Ammonium between Plant-Roots and Nitrifying and Heterotrophic Bacteria and the Effects of Protozoan Grazing

    NARCIS (Netherlands)

    Verhagen, F.J.M.; Laanbroek, H.J.; Woldendorp, J.W.

    1995-01-01

    The competition for limiting amounts of ammonium between the chemolithotrophic ammonium-oxidizing species Nitrosomonas europaea, the heterotrophic species Arthrobacter globiformis and roots of Plantago lanceolata (Ribwort plantain) was studied in a series of model systems of increasing complexity, i

  4. Environmental Factors Affecting Ammonium Oxidation Under Iron Reducing Conditions

    Science.gov (United States)

    Jaffe, P. R.; Huang, S.; Ruiz-Urigüen, M.

    2014-12-01

    Ammonium (NH4+) oxidation coupled to iron (Fe) reduction in the absence of oxygen and nitrate/nitrite (NO3-/NO2-) has been reported by several investigators and referred to as Feammox. Feammox is a biological reaction, where Fe(III) is the electron acceptor, which is reduced to Fe(II), and NH4+ is the electron donor, which is oxidized to NO2-. Through a 180-day anaerobic incubation experiment, and using PCR-DGGE, 454-pyosequecing and qPCR analysis, we have shown that an Acidimicrobiaceae bacterium A6, a previously unreported species in the Acidimicrobiaceae family, might be either responsible or plays a key role in the Feammox process, We have enriched these Feammox bacteria (65.8% in terms of cell numbers) in a membrane reactor, and isolated the pure Acidimicrobiaceae bacterium A6 strain in an autotrophic medium. In samples collected and then incubated from a series of local wetland-, upland-, as well as storm-water detention pond-sediments, Feammox activity was only detected in acidic soil environments that contain Fe oxides. Using primers we developed for this purpose, Acidimicrobiaceae bacterium A6 was detected in all incubations where Feammox was observed. Anaerobic incubations of Feammox enrichment cultures adjusted to different pH, revealed that the optimal pH for Feammox is 4 ~ 5, and the reaction does not proceed when pH > 7. Feammox was still proceeding at pH as low as 2. In Feammox culture amended with different Fe(III) sources, Feammox reaction proceeded only when Fe oxides (ferrihydrite or goethite ) were supplied, whereas samples incubated with ferric chloride or ferric citrate showed no measurable NH4+ oxidation. Furthermore, we have also determined from incubation experiments conducted with a temperature gradient (10 ~ 35℃), that the Feammox process was active when the temperature is above 15℃, and the optimal temperature is 20℃. Incubations of enrichment culture with 79% Feammox bacteria appeared to remove circa 8% more NH4+ at 20ºC than at

  5. Quaternary ammonium derivatives as spasmolytics for irritable bowel syndrome.

    Science.gov (United States)

    Evangelista, S

    2004-01-01

    Quaternary ammonium derivatives such as cimetropium, n-butyl scopolammonium, otilonium and pinaverium bromide have been discovered and developed as potent spasmolytics of the gastrointestinal tract. Their pharmacological activity has been proven in both "in vivo" and "in vitro" studies of hypermotility. "In vitro" experiments showed that they possess antimuscarinic activity at nM level but only pinaverium and otilonium are endowed with calcium channel blocker properties. These latter compounds relaxed the gastrointestinal smooth muscle mainly through a specific inhibition of calcium ion influx through L-type voltage operated calcium channels. Molecular pharmacology trials have indicated that pinaverium and otilonium can bind specific subunits of the calcium channel in the external surface of the plasma membrane and in this way they block the machinery of the contraction. Recent evidence showed that otilonium is able to bind tachykinin NK(2) receptors and not only inhibits one of the major contractile agents but can reduce the activation of afferent nerves devoted to the passage of sensory signals from the periphery to the central nervous system. Thanks to their typical physico-chemical characteristics, they are poorly absorbed by the systemic circulation and generally remain in the gastrointestinal tract where they exert the muscle relaxant activity by a local activity. Some differences exists in the absorption among these compounds: both n-butyl scopolammonium and cimetropium are partially taken up in the bloodstream, pinaverium has a low absorption (8-10 %) but is endowed with an excellent hepato-biliary excretion and otilonium, which has the lowest absorption (3 %), is almost totally excreted by faeces. Quaternary ammonium derivatives are widely used for the treatment of irritable bowel syndrome and recent meta-analyses have supported their efficacy in this disease. Due to its therapeutic index, the use of n-butyl scopolammonium is more indicated to treat acute

  6. Synthesis and Antimicrobial Properties of the Novel Fluorinated Bis-ammonium Salts with Two Primary Amine Groups

    Institute of Scientific and Technical Information of China (English)

    Jian Bin LUO; Qiang WANG; Hong TAN; Jie Hua LI; Yin Ping ZHONG

    2006-01-01

    In order to resolve the increasing resistance phenomena of the Gram-negative bacteria against single chain quaternary ammonium salts (QAS), lysine with a pedant fluorinated bis-ammonium salts was synthesized and its antimicrobial properties were evaluated in this work.The novel fluorinated bis-ammonium salts shows similar activity with conventional single chain quaternary ammonium salts against Gram-positive bacteria but stronger activity against Gram-negative bacteria and yeast compared with the single chained counterpart.

  7. Relating dynamic conditions to the performance of biological rapid sand filters used to remove ammonium, iron, and manganese from drinking water

    DEFF Research Database (Denmark)

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

    and media samples were collected throughout the depth of the column and over the operational cycle of the columns. Substrate analysis included ammonium, nitrite, nitrate, iron, and manganese. Qpcr analysis were also performed to quantify ammonium oxidizing bacteria (AOBs), ammonium oxidizing archea ( AOAs...... on the roles of both Ammonium oxidizing bacteria (AOBs) and Ammonium oxidizing archea (AOAs) in the biological removal of ammonium in rapid sand filters and how varying substrate loadings and operating conditions can affect the biological performance of these filters....

  8. Paleosols in central Illinois as potential sources of ammonium in groundwater

    Science.gov (United States)

    Glessner, J.J.G.; Roy, W.R.

    2009-01-01

    Glacially buried paleosols of pre-Holocene age were evaluated as potential sources for anomalously large concentrations of ammonium in groundwater in East Central Illinois. Ammonium has been detected at concentrations that are problematic to water treatment facilities (greater than 2.0 mg/L) in this region. Paleosols characterized for this study were of Quaternary age, specifically Robein Silt samples. Paleosol samples displayed significant capacity to both store and release ammonium through experiments measuring processes of sorption, ion exchange, and weathering. Bacteria and fungi within paleosols may significantly facilitate the leaching of ammonium into groundwater by the processes of assimilation and mineralization. Bacterial genetic material (DNA) was successfully extracted from the Robein Silt, purified, and amplified by polymerase chain reaction to produce 16S rRNA terminal restriction fragment length polymorphism (TRFLP) community analyses. The Robein Silt was found to have established diverse and viable bacterial communities. 16S rRNA TRFLP comparisons to well-known bacterial species yielded possible matches with facultative chemolithotrophs, cellulose consumers, nitrate reducers, and actinomycetes. It was concluded that the Robein Silt is both a source and reservoir for groundwater ammonium. Therefore, the occurrence of relatively large concentrations of ammonium in groundwater monitoring data may not necessarily be an indication of only anthropogenic contamination. The results of this study, however, need to be placed in a hydrological context to better understand whether paleosols can be a significant source of ammonium to drinking water supplies. ?? 2009 National Ground Water Association.

  9. Preparation and characteristic research of anhydrous magnesium chloride with dehydrated ammonium carnallite

    Institute of Scientific and Technical Information of China (English)

    ZHOU Ning-bo; CHEN Bai-zhen; HE Xin-kuai; LI Yi-bing

    2006-01-01

    Taking the saline lake bischofite and NH4Cl that was removed with the ammonia method and continuwas synthesized. And then the ammonium carnallite was dehydrated to some extent at 160℃ for 4 h. Ammonium carnallite reacted with ammonia at 240℃ for 150 min and the ammonation ammonium carnallite was produced. Finally, the ammonation ammonium carnallite was calcined at 750℃ into anhydrous magnesium chloride containing only 0.1% (mass fraction) of MgO. On the other hand, dehydrated ammonium carnallite was mixed with the solid ammonium chloride at mass ratio 1:4 at high temperature and with the differential pressure of HN3 above 30.5 kPa. The dehydrated ammonium carnallite of mixture was dehydrated at 410℃, and then calcined at 700℃ into anhydrous magnesium chloride with only 0. 087% (mass fraction) of MgO. X-ray diffraction and electron microscopy analysis results prove that anhydrous magnesium chloride obtained by both methods hasn't mixed phases, the particle is large and even has good dispersion, which is suitable for preparation of metal magnesium in the electrolysis.

  10. Coastal water column ammonium and nitrite oxidation are decoupled in summer

    Science.gov (United States)

    Heiss, Elise M.; Fulweiler, Robinson W.

    2016-09-01

    Water column nitrification is a key process in the nitrogen cycle as it links reduced and oxidized forms of nitrogen and also provides the substrate (nitrate) needed for reactive nitrogen removal by denitrification. We measured potential water column ammonium and nitrite oxidation rates at four sites along an estuary to continental shelf gradient over two summers. In most cases, nitrite oxidation rates outpaced ammonium oxidation rates. Overall, ammonium and nitrite oxidation rates were higher outside of the estuary, and this trend was primarily driven by higher oxidation rates in deeper waters. Additionally, both ammonium and nitrite oxidation rates were impacted by different in situ variables. Ammonium oxidation rates throughout the water column as a whole were most positively correlated to depth and salinity and negatively correlated to dissolved oxygen and light. In contrast, nitrite oxidation rates throughout the water column were negatively correlated with light and pH. Multivariate regression analysis revealed that while both surface (20 m) ammonium oxidation rates were most strongly predicted by depth and light, surface rates were also regulated by salinity and deep rates by temperature. Surface (20 m) nitrite oxidation rates. These results support the growing body of evidence that ammonium oxidation and nitrite oxidation are not always coupled, should be measured separately, and are influenced by different environmental conditions.

  11. Root ABA Accumulation Enhances Rice Seedling Drought Tolerance under Ammonium Supply: Interaction with Aquaporins

    Science.gov (United States)

    Ding, Lei; Li, Yingrui; Wang, Ying; Gao, Limin; Wang, Min; Chaumont, François; Shen, Qirong; Guo, Shiwei

    2016-01-01

    In previous studies, we demonstrated that ammonium nutrition enhances the drought tolerance of rice seedlings compared to nitrate nutrition and contributes to a higher root water uptake ability. It remains unclear why rice seedlings maintain a higher water uptake ability when supplied with ammonium under drought stress. Here, we focused on the effects of nitrogen form and drought stress on root abscisic acid (ABA) concentration and aquaporin expression using hydroponics experiments and stimulating drought stress with 10% PEG6000. Drought stress decreased the leaf photosynthetic rate and stomatal conductivity and increased the leaf temperature of plants supplied with either ammonium or nitrate, but especially under nitrate supply. After 4 h of PEG treatment, the root protoplast water permeability and the expression of root PIP and TIP genes decreased in plants supplied with ammonium or nitrate. After 24 h of PEG treatment, the root hydraulic conductivity, the protoplast water permeability, and the expression of some aquaporin genes increased in plants supplied with ammonium compared to those under non-PEG treatment. Root ABA accumulation was induced by 24 h of PEG treatment, especially in plants supplied with ammonium. The addition of exogenous ABA decreased the expression of PIP and TIP genes under non-PEG treatment but increased the expression of some of them under PEG treatment. We concluded that drought stress induced a down-regulation of aquaporin expression, which appeared earlier than did root ABA accumulation. With continued drought stress, aquaporin expression and activity increased due to root ABA accumulation in plants supplied with ammonium.

  12. The ammonium content in the Malayer igneous and metamorphic rocks (Sanandaj-Sirjan Zone, Western Iran)

    Science.gov (United States)

    Ahadnejad, Vahid; Hirt, Ann Marie; Valizadeh, Mohammad-Vali; Bokani, Saeed Jabbari

    2011-04-01

    The ammonium (NH4+) contents of the Malayer area (Western Iran) have been determined by using the colorimetric method on 26 samples from igneous and metamorphic rocks. This is the first analysis of the ammonium contents of Iranian metamorphic and igneous rocks. The average ammonium content of metamorphic rocks decreases from low-grade to high-grade metamorphic rocks (in ppm): slate 580, phyllite 515, andalusite schist 242. In the case of igneous rocks, it decreases from felsic to mafic igneous types (in ppm): granites 39, monzonite 20, diorite 17, gabbro 10. Altered granitic rocks show enrichment in NH4+ (mean 61 ppm). The high concentration of ammonium in Malayer granites may indicate metasedimentary rocks as protoliths rather than meta-igneous rocks. These granitic rocks (S-types) have high K-bearing rock-forming minerals such as biotite, muscovite and K-feldspar which their potassium could substitute with ammonium. In addition, the high ammonium content of metasediments is probably due to inheritance of nitrogen from organic matter in the original sediments. The hydrothermally altered samples of granitic rocks show highly enrichment of ammonium suggesting external sources which intruded additional content by either interaction with metasedimentary country rocks or meteoritic solutions.

  13. Antibacterial Activity of Dental Cements Containing Quaternary Ammonium Polyethylenimine Nanoparticles

    Directory of Open Access Journals (Sweden)

    Nurit Beyth

    2012-01-01

    Full Text Available Glass ionomer cements (GICs are commonly used for cementing full cast crown restorations. Regrettably, although the dental cements fill the gap between the tooth and the crown, bacterial microleakage may occur, resulting in secondary caries. As microleakage cannot be completely prevented, GICs possessing antibacterial properties are in demand. In the present study the antibacterial activity of insoluble, cross-linked quaternary ammonium polyethylenimine (QPEI nanoparticles incorporated at 1% w/w in two clinically available GICs were studied. The antibacterial activity was tested against Streptococcus mutans and Lactobacillus casei using the direct contact test (DCT and the agar diffusion test (ADT. Using the direct contact test, antibacterial activity (<0.05 was found in both tested GICs with incorporated QPEI nanoparticles, the effect lasting for at least one month. However, the ADT showed no inhibition halo in the test bacteria, indicating that the antimicrobial nanoparticles do not diffuse into the agar. The results show that the incorporation of QPEI nanoparticles in glass ionomer cements has a long-lasting antibacterial effect against Streptococcus mutans and Lactobacillus casei. Changing the antibacterial properties of glass ionomer cements by incorporating QPEI antibacterial nanoparticles may prolong the clinical performance of dental crowns.

  14. 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.

  15. 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.

  16. Evaluation of a cesium adsorbent grafted with ammonium 12-molybdophosphate

    Science.gov (United States)

    Shibata, Takuya; Seko, Noriaki; Amada, Haruyo; Kasai, Noboru; Saiki, Seiichi; Hoshina, Hiroyuki; Ueki, Yuji

    2016-02-01

    A fibrous cesium (Cs) adsorbent was developed using radiation-induced graft polymerization with a cross-linked structure containing a highly stable adsorption ligand. The ligand, ammonium 12-molybdophosphate (AMP), was successfully introduced onto the fibrous polyethylene trunk material. The resulting Cs adsorbent contained 36% nonwoven fabric polyethylene (NFPE), 1% AMP, 2% triallyl isocyanurate (TAIC) and 61% glycidyl methacrylate (GMA). The adsorbent's Cs adsorption capacity was evaluated using batch and column tests. It was determined that the adsorbent could be used in a wide pH range. The amount of desorbed molybdenum, which can be used as an estimate for AMP stability on the Cs adsorbent, was minimized at the standard drinking water pH range of 5.8-8.6. Based from the inspection on the adherence of these results to the requirements set forth by the Food Sanitation Act by a third party organization, it can be concluded that the developed Cs adsorbent can be safely utilized for drinking water.

  17. Evaluation of ammonium polyphosphate fertilizer as a carrier of zinc

    International Nuclear Information System (INIS)

    Ammonium polyphosphate (APP) and diammonium orthophosphate (DAP) were evaluated as carriers of zinc in an Ultisol and a Vertisol. Surface applications of 65Zn along with urea or orthophosphate or pyrophosphate or polyphosphate to the two soils indicated very little movement of the radionuclide below 2 cm from surface in both soils on leaching with rain water. Greenhouse experiments with maize and red kidney beans grown in sequence in the two soils fertilized with APP and DAP both blended with 65Zn (as ZnSO4.7H2O) indicated that while the Zn fertilizer use efficiency of Zn-APP blend was significantly higher than that of Zn-DAP blend for maize, their residual value was equal for the succeeding bean crop. Experiments with maize-greengram sequence indicated superiority of Zn-APP blend only in Vertisol, while in Ultisol both the blends were equally effective. A field experiments with flooded rice indicated increased grain yield with application of Zn at 22 kg Zn ha-1. Neither P nor Zn application had any significant effect on straw yield. Grain and straw Zn concentrations increased significantly by the applications of both P and Zn. At zero or low levels of applied Zn, APP was significantly superior to DAP as a P source; while at higher dose of Zn, no significant difference was noted between the two P sources. (author). 18 refs, 5 tabs

  18. Rubidium, cesium and potassium sorption with magnesium-ammonium phosphate

    Energy Technology Data Exchange (ETDEWEB)

    Leont' eva, G.V.; Tomchuk, T.K.

    1986-01-01

    The possibility for using magnesium-ammonium phosphate as a sorbent to separate Cs/sup +/, Rb/sup +/ and K/sup +/ ions is estimated. The sorbent composition is close to NH/sub 4/MgPO/sub 4/x6H/sub 2/O. Sorption isotherms have been removed under static conditions at 293+-2 K separately for Cs/sup +/, Rb/sup +/ and K/sup +/ ions. Determination of the separation coefficients of these Cs/sup +/-Rb/sup +/ and Rb/sup +/-K/sup +/ ion pairs (the ratio of the ions separated in the initial solution varies from 1:1 to 1:10) during their sorption by NH/sub 4/MgPO/sub 4/x6H/sub 2/O phosphate gave the following estimation of the values measured: P/sub Cs-Rb/=(30-156) and P/sub Rb-K/=(7-15). Taking into account high values of the separation coefficients and good reversibility of the ion exchange process NH/sub 4//sup +/reversibleMe/sup +/(Me/sup +/=Cs/sup +/, Rb/sup +/, K/sup +/) by phosphate and with the struvite structure, it is possible to recommend this sorbent for practical application.

  19. Photoluminescence from silicon nanoparticles embedded in ammonium silicon hexafluoride

    Energy Technology Data Exchange (ETDEWEB)

    Kalem, Seref [UEKAE, National Research Institute of Electronics and Cryptology, Gebze 41470 Kocaeli (Turkey); Werner, Peter; Becker, Michael; Zakharov, Nikolai [Department of Experimental Physics, Max-Planck-Institute, Halle(Saale) (Germany); Talalaev, Vadim [ZIK ' SiLi-nano' , Martin-Luther-Universitaet (Halle), Karl-Freiherr-von-Fritsch-Strasse 3 D-06120 Halle (Germany); Arthursson, Oerjan, E-mail: s.kalem@uekae.tubitak.gov.tr [Microtechnology and Nanosciences Department, Chalmers University of Technology, Goeteborg (Sweden)

    2010-10-29

    Silicon (Si) nanoparticles (NPs) were synthesized by transforming a Si wafer surface to ammonium silicon hexafluoride (ASH) or (NH{sub 4}){sub 2}SiF{sub 6} under acid vapor treatment. Si-NPs which were found to be embedded within the polycrystalline (ASH) layer exhibit a strong green-orange photoluminescence (PL). Differential PL measurements revealed a major double component spectrum consisting of a broad band associated with the ASH-Si wafer interfacial porous oxide layer and a high energy band attributable to Si-NPs embedded in the ASH. The origin of the latter emission can be explained in terms of quantum/spatial confinement effects probably mediated by oxygen related defects in or around Si-NPs. Although Si-NPs are derived from the interface they are much smaller in size than those embedded within the interfacial porous oxide layer (SiO{sub x}, x > 1.5). Transmission electron microscopy (TEM) combined with Raman scattering and Fourier transformed infrared (FTIR) analysis confirmed the presence of Si-NP and Si-O bondings pointing to the role of oxygen related defects in a porous/amorphous structure. The presence of oxygen of up to 4.5 at.% in the (NH{sub 4}){sub 2}SiF{sub 6} layer was confirmed by energy dispersive spectroscopy (EDS) analysis.

  20. Synthesis, Characterization and Thermal Decomposition Mechanism of Cetyltrimethyl Ammonium Tetrathiotungstate

    Institute of Scientific and Technical Information of China (English)

    Gaojun An; Yunqi Liu; Yongming Chai; Hongyan Shang; Chenguang Liu

    2006-01-01

    The synthesis, characterization and thermal decomposition mechanism of cetyltrimethyl ammonium tetrathiotungstate (CTriMATT) were studied herein. The as-synthesized CTriMATT was characterized by Elemental analysis, X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Ultraviolet visible (UV-Vis) spectra. The results showed that the as-synthesized CTriMATT had high purity and good crystallinity. The introduction of alkyl groups induced a shift of the stretching vibration band of W-S bond to lower wavenumber, while it had no influence on the position of WS2-4. Thermogravimetric analysis (TG), differential thermal analysis (DTA) and in situ XRD characterizations revealed that CTriMATT began to decompose at 423 K in nitrogen and was converted to WS2 eventually. In addition,the decomposition product of CTriMATT at 673 K in nitrogen was characterized by N2 adsorption (BET)and scanning electron microscopy (SEM). The results demonstrated that WS2 with higher specific surface area, and pore volume could be obtained from the thermal decomposition of CTriMATT in nitrogen.

  1. Betaines and related ammonium compounds in chestnut (Castanea sativa Mill.).

    Science.gov (United States)

    Servillo, Luigi; Giovane, Alfonso; Casale, Rosario; Balestrieri, Maria Luisa; Cautela, Domenico; Paolucci, Marina; Siano, Francesco; Volpe, Maria Grazia; Castaldo, Domenico

    2016-04-01

    Chestnut fruits, being poor of simple sugars and consisting mainly of fibers and starch, are among the constituents of Mediterranean diet. While numerous studies report on content of proteins and amino acids in chestnut, no one has appeared so far on betaines, an important class of nitrogen compounds ubiquitous in plants for their protective action in response to abiotic stress. In this study, we analyzed by HPLC-ESI-tandem mass spectrometry, in fruits and flours of varieties of chestnut cultivated in Italy, the composition of betaines and ammonium compounds intermediates of their biosynthesis. Besides the parent amino acids, the compounds quantified were choline, glycerophosphocholine, phosphocholine, glycine betaine, N-methylproline, proline betaine (stachydrine), β-alanine betaine, 4-guanidinobutyric acid, trigonelline, N,N,N-trimethyllysine. Interestingly, some uncommon derivatives of pipecolic acid, such as N-methylpipecolic acid, 4-hydroxypipecolic acid and 4-hydroxy-N-methylpipecolic acid were identified for the first time in chestnut samples and characterized by MS(n) tandem mass spectrometry.

  2. Organomontmorillonites Modified with 2-Methacryloyloxy Ethyl Alkyl Dimethyl Ammonium Bromide

    Institute of Scientific and Technical Information of China (English)

    WANG Jian-quan; WU Wen-hui

    2007-01-01

    Organomontmorillonites (organo-MMT) were synthesized by means of montmorillonites (MMT) modified with a series of 2-methacryloyloxy ethyl alkyl dimethyl ammonium bromide (MAAB) having different alkyl chain lengths as cationic surfactants through a cationic exchanging reaction, and were characterized by FTIR, TG, elemental analysis, and XRD. The microenvironment of the organic interlayer such as the orientation and arrangement of the alkyl chains of MAAB, as well as the properties of nanocomposite hydrogels, were also investigated. The amount of organic components absorbed on interlayer and the basal spacing of organo-MMT both increase with the increasing of alkyl length of MAAB. When carbon number of alkyl chain is in the region of 8 to 14, the alkyl chains between layers would adopt a disordered gauche conformation; while the carbon number is 16, an ordered all-trans conformation with a vertical orientation would be found together with the disordered gauche conformation according to the results of XRD and FTIR. Due to the difference of microenvironment of organic interlayer, the Young's moduli of the nanocomposite hydrogels increased as the alkyl chains of MAAB became longer.

  3. Interaction of ochratoxin A with quaternary ammonium beta-cyclodextrin.

    Science.gov (United States)

    Poór, Miklós; Kunsági-Máté, Sándor; Szente, Lajos; Matisz, Gergely; Secenji, Györgyi; Czibulya, Zsuzsanna; Kőszegi, Tamás

    2015-04-01

    Ochratoxin A (OTA) is a widely spread nephrotoxic food contaminant mycotoxin. Unfortunately, attenuation or prevention of the toxic effects of OTA is still an unresolved problem. Molecular inclusion of OTA by cyclodextrins (CDs) results in complexes with low stability. In the human organism, OTA exists mostly in the dianionic state (OTA(2-)). Therefore, our major goal was to develop a chemically modified cyclodextrin which gives a more stable complex with OTA than the previously published derivatives and which shows stronger preference towards OTA(2-). In our fluorescence spectroscopic study we demonstrate that quaternary ammonium beta-cyclodextrin (QABCD) fulfils both of these requirements. The calculated stability constant of the QABCD-OTA(2-) complex was 28,840 M(-1) (about 200-fold higher than that of the β-CD-OTA(2-) complex). We hypothesize, that QABCD may be a suitable tool for the decontamination of different OTA-contaminated drinks; furthermore, for alleviation of the toxic effects of OTA, such complex formation may reduce its absorption from the intestine.

  4. Thermochemical Properties and Decomposition Kinetics of Ammonium Magnesium Phosphate Monohydrate

    Institute of Scientific and Technical Information of China (English)

    WU,Jian; YUAN,Ai-Qun; HUANG,Zai-Yin; TONG,Zhang-Fa; CHEN,Jie; LIANG,Rong-Lan

    2007-01-01

    Ammonium magnesium phosphate monohydrate NH4MgPO4·H2O was prepared via solid state reaction at room temperature and characterized by XRD, FT-IR and SEM. Thermochemical study was performed by an isoperibol solution calorimeter, non-isothermal measurement was used in a multivariate non-linear regression analysis to determine the kinetic reaction parameters. The results show that the molar enthalpy of reaction above is (28.795±0.182) kJ/mol (298.15 K), and the standard molar enthalpy of formation of the title complex is (-2185.43±13.80)kJ/mol (298.15 K). Kinetics analysis shows that the second decomposition of NH4MgPO4·H2O acts as a double-step reaction: an nth-order reaction (Fn) with n=4.28, E1=147.35 kJ/mol, A1=3.63×1013 s-1 is followed by a second-order reaction (F2) with E2=212.71 kJ/mol, A2= 1.82×1018 s-1.

  5. Interaction of ochratoxin A with quaternary ammonium beta-cyclodextrin.

    Science.gov (United States)

    Poór, Miklós; Kunsági-Máté, Sándor; Szente, Lajos; Matisz, Gergely; Secenji, Györgyi; Czibulya, Zsuzsanna; Kőszegi, Tamás

    2015-04-01

    Ochratoxin A (OTA) is a widely spread nephrotoxic food contaminant mycotoxin. Unfortunately, attenuation or prevention of the toxic effects of OTA is still an unresolved problem. Molecular inclusion of OTA by cyclodextrins (CDs) results in complexes with low stability. In the human organism, OTA exists mostly in the dianionic state (OTA(2-)). Therefore, our major goal was to develop a chemically modified cyclodextrin which gives a more stable complex with OTA than the previously published derivatives and which shows stronger preference towards OTA(2-). In our fluorescence spectroscopic study we demonstrate that quaternary ammonium beta-cyclodextrin (QABCD) fulfils both of these requirements. The calculated stability constant of the QABCD-OTA(2-) complex was 28,840 M(-1) (about 200-fold higher than that of the β-CD-OTA(2-) complex). We hypothesize, that QABCD may be a suitable tool for the decontamination of different OTA-contaminated drinks; furthermore, for alleviation of the toxic effects of OTA, such complex formation may reduce its absorption from the intestine. PMID:25442535

  6. The Structure of Ammonium D,L-Tartrate

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The single crystals of the title compound NH4+C4H5O6- (C4H9NO6, Mr = 167.1) were obtained from a hot aqueous solution containing L-glutamine and D,L-tartaric acid in mole ratio1:1.5. The crystal belongs to monoclinic space group P21/c with a = 7.646(2), b = 7.804(2), c = 11.502(3)?, β = 102.26(2)o, V = 670.7(3)?3, Z = 4, F(000) = 352, Dc = 1.655 g.cm-3, ((MoK() = 0.16 mm-1, R = 0.035, wR = 0.094 for 1028 observed reflections (I>2((I)). The enatiomeric anions of the tartrate with both (2S,3S)- and (2R,3R)-configuration co-exist in the unit cell. The carbon skeleton assumes a coplanar arrangement with a torsion angle of 181.5o. The three- dimensional H-bonding network exists in the crystal. While tartrate groups link each other by H-bonds between carboxyl and hydroxyl groups, the ammonium cations insert between the tartrate groups to form a sandwich-like crystal structure.

  7. Proton transfer in gas-phase ammonium dinitramide clusters

    Science.gov (United States)

    Alavi, Saman; Thompson, Donald L.

    2003-02-01

    Proton transfer in gaseous ammonium dinitramide (ADN) clusters up to (ADN)2 is studied by using density-functional theory. Proton transfer between the hydrogen dinitramide and ammonia units does not occur in the ADN monomer, rather the ammonia-hydrogen dinitramide complex is stabilized by strong hydrogen bonding. However, proton transfer between hydrogen dinitramide and ammonia is observed in the ADN dimer [NH3HN(NO2)2]2, ADN solvated with a single ammonia molecule [NH3NH(NO2)2]NH3, and ADN solvated with a hydrogen dinitramide molecule [NH3HN(NO2)2]HN(NO2)2. Structural changes in the complexes relative to the free molecules and the binding energies of the clusters are given. Using population analysis, the total electrostatic interaction energy in each cluster is calculated. The electrostatic energy is a measure that distinguishes between the ionic or hydrogen-bonded nature of the clusters. Some implications of proton transfer in ADN clusters on the decomposition mechanism of ADN are discussed.

  8. Atmospheric transport and wet deposition of ammonium in North Carolina

    Science.gov (United States)

    Walker, John T.; Aneja, Viney P.; Dickey, David A.

    Wet deposition and transport analysis has been performed for ammonium (NH 4+) in North Carolina, USA. Multiple regression analysis is employed to model the temporal trend and seasonality in monthly volume-weighted mean NH 4+ concentrations in precipitation from 1983 to 1996 at six National Atmospheric Deposition Program/National Trends Network (NADP/NTN) sites. A significant ( ppopulated network of swine and poultry operations. This trend is positively correlated with increasing ammonia (NH 3) emissions related to the vigorous growth of North Carolina's swine population since 1990, particularly in the state's Coastal Plain region. A source-receptor regression model, which utilizes weekly NH 4+ concentrations in precipitation in conjunction with boundary layer air mass back trajectories, is developed to statistically test for the influence of a particular NH 3 source region on NH 4+ concentrations at surrounding NADP/NTN sites for the years 1995-1996. NH 3 emissions from this source region, primarily evolving from swine and poultry operations, are found to increase NH 4+ concentration in precipitation at sites up to ≈80 km away. At the Scotland County (NC36) and Wake County (NC41) sites, mean NH 4+ concentrations show increases of at least 44% for weeks during which 25% or more back trajectories are influenced by this source region.

  9. 电镀废水中硫氰酸根离子含量的自动电位滴定%Determination of Thiocyanate Ions in Electroplating Wastewater by Automatic Potentiometeric Titration

    Institute of Scientific and Technical Information of China (English)

    姚晓华; 丘圣; 丘山; 丘星初

    2011-01-01

    The condition and method to determine thiocyanate ion by automatic potentiometric titration was studied. The results show that, the selection of silver electrode as indicator electrode, the electrode 217 with double liquid junction as reference, this method has high selectivity in nitric acid medium to titrate thiocyanate ion. When used in electroplating wastewater analysis, the method is simple and fast, which can print out the results in 4 minutes.%研究了用自动电位滴定测定硫氰酸根离子的条件和方法.实验结果表明,选用银电极为指示电极,217型双液接电极为参比电极,在硝酸介质中滴定硫氰酸根离子,方法具有高选择性;应用于电镀废水分析,方法简便快捷,在4min内能打印出分析结果.

  10. Effects of High Ammonium Concentration on Growth and Nutrient Uptake of Lettuce Plants with Solution Culture

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    A nutrition solution experiment was conducted over two months to investigate the response of vegetable crops to high concentrations of ammonium, using lettuce (Lactuca sativa L. cv. Angustana Irish) as a test crop. Ammonium concentrations were designed in 5 levels, ranging from 12 mmol N L-1 to 22 mmol N L-1 and local tap water was used as water source. At the first culture stage (0-9 days), lettuce plants maintained normal growth while the lettuce roots were increasingly impaired. During the subsequent three stages the root structure was greatly damaged, and roots became brown or black through continuous supply of high concentration of ammonium. However, there was no obvious reduction of the aboveground biomass of the plants in the high ammonium treatments compared to those supplied with nitrate alone. In contrast to results obtained in another experiment from us with distilled water, the detrimental effect of high ammonium concentration on lettuce growth was greatly alleviated. Based on the results, it was postulated that the small amount of nitrate and the higher amount of bicarbonate existed in the tap water might mitigate the adverse effects of high ammonium N. The higher bicarbonate content in water and soil has usually been regarded as a major constraint factor limiting plant growth in calcareous soil areas. However, the reaction of bicarbonate to ammonium might produce positively interactive effect on reduction of both damages. The lettuce plants grown in ammonium solutions took up less P, K, Fe, Mn and Cu and more Ca than those grown in the nitrate nutrient solution. In conclusion, the results indicated that the N form imposed an obvious influence on absorption of cations and anions. Supplying ammonium-N stimulated transport of Ca, Mg and Mn to shoots of lettuce.

  11. Natural attenuation potential of tricholoroethene in wetland plant roots: role of native ammonium-oxidizing microorganisms.

    Science.gov (United States)

    Qin, Ke; Struckhoff, Garrett C; Agrawal, Abinash; Shelley, Michael L; Dong, Hailiang

    2015-01-01

    Bench-scale microcosms with wetland plant roots were investigated to characterize the microbial contributions to contaminant degradation of trichloroethene (TCE) with ammonium. The batch system microcosms consisted of a known mass of wetland plant roots in aerobic growth media where the roots provided both an inoculum of root-associated ammonium-oxidizing microorganisms and a microbial habitat. Aqueous growth media, ammonium, and TCE were replaced weekly in batch microcosms while retaining roots and root-associated biomass. Molecular biology results indicated that ammonium-oxidizing bacteria (AOB) were enriched from wetland plant roots while analysis of contaminant and oxygen concentrations showed that those microorganisms can degrade TCE by aerobic cometabolism. Cometabolism of TCE, at 29 and 46 μg L(-1), was sustainable over the course of 9 weeks, with 20-30 mg L(-1) ammonium-N. However, at 69 μg L(-1) of TCE, ammonium oxidation and TCE cometabolism were completely deactivated in two weeks. This indicated that between 46 and 69 μg L(-1) TCE with 30 mg L(-1) ammonium-N there is a threshold [TCE] below which sustainable cometabolism can be maintained with ammonium as the primary substrate. However, cometabolism-induced microbial deactivation of ammonium oxidation and TCE degradation at 69 μg L(-1) TCE did not result in a lower abundance of the amoA gene in the microcosms, suggesting that the capacity to recover from TCE inhibition was still intact, given time and removal of stress. Our study indicates that microorganisms associated with wetland plant roots can assist in the natural attenuation of TCE in contaminated aquatic environments, such as urban or treatment wetlands, and wetlands impacted by industrial solvents.

  12. Noncovalent Complexation of Monoamine Neurotransmitters and Related Ammonium Ions by Tetramethoxy Tetraglucosylcalix[4]arene

    Science.gov (United States)

    Torvinen, Mika; Kalenius, Elina; Sansone, Francesco; Casnati, Alessandro; Jänis, Janne

    2012-02-01

    The noncovalent complexation of monoamine neurotransmitters and related ammonium and quaternary ammonium ions by a conformationally flexible tetramethoxy glucosylcalix[4]arene was studied by electrospray ionization Fourier transform ion cyclotron resonance (ESI-FTICR) mass spectrometry. The glucosylcalixarene exhibited highest binding affinity towards serotonin, norepinephrine, epinephrine, and dopamine. Structural properties of the guests, such as the number, location, and type of hydrogen bonding groups, length of the alkyl spacer between the ammonium head-group and the aromatic ring structure, and the degree of nitrogen substitution affected the complexation. Competition experiments and guest-exchange reactions indicated that the hydroxyl groups of guests participate in intermolecular hydrogen bonding with the glucocalixarene.

  13. Rotational barriers in ammonium hexachlorometallates as studied by NMR, tunneling spectroscopy and ab initio calculations

    DEFF Research Database (Denmark)

    Birczynski, A.; Lalowicz, Z.T.; Lodziana, Zbigniew

    2004-01-01

    Ammonium hexachlorometallates, (NH4)(2)MCl6 With M = Pd, Pt, Ir, Os, Re, Se, Sn, Te and Pb, comprise a set of compounds with systematically changing properties. The compounds may be ordered according to decreasing tunnelling frequency (TF) of ammonium ions, which is related to the increasing...... structure explain observed variation of the tunnelling frequencies for NH4+. The theory provides also M-Cl distances and barriers for C-2 and C-3 rotations of ammonium ions in respective compounds, which show good agreement with experimental values. (C) 2004 Elsevier B.V. All rights reserved....

  14. Volatile Corrosion Inhibitors Part III- Ammonium stearate and M-Dinitrobenezene

    Directory of Open Access Journals (Sweden)

    K. S. Rajagopalan

    1962-07-01

    Full Text Available In earlier studies while screening various chemical compound for their vapour phase inhibiting properties. Some ammonium salts and nitro-compounds had shown promising results. Of these, ammonium stearate and m-dinitrobenzene gave the best results in accelerated short term tests. In the present paper a more detailed investigation on the corrosion protection given by them has been made.Ammonium stearate and m-dinitrobenzene, both, have been found to perform satisfactorily under all test conditions except SOsub2 test where m-dinitrobenzene failed. Their indigenous availability, low cost and good corrosion inhibiting properties demands favorable consideration for their adoption as VCIs for general use.

  15. Effect of ammonium nutrition on the nitrate utilization, nitrate reductase actvity and growth of Spirodela polyrrhiza

    Directory of Open Access Journals (Sweden)

    Ewa Tatkowska

    2014-02-01

    Full Text Available The influence of NH4+ ions on nitrate assimilation and growth of sterile Spirodela polyrrhiza cultures was investigated. S. polyrrhiza utilises both the nitrate and the ammonium form of nitrogen, it prefers, however, NH4+. Ammonium ions present in the nitrate medium inhibit the activity of nitrate reductase (NR, but they do not affect enzyme 'induction and only slightly reduce N03- uptake. These results sugest that the inhibitory effect of NH4+ on the NR activity is the main cause of the decrease in N03- assimilation by S. polyrrhiza cultures growing in nitrate-ammonium medium.

  16. an investigation of the ammonium poly uranate precipitation via uranyl nitrate solution

    International Nuclear Information System (INIS)

    a series of experiments were made concerning the interaction of uranyl nitrate with ammonium hydroxide solution, with the aim of preparing ammonium poly uranate (APU) as an intermediate product during nuclear reactors fuel fabrication. the particle size and final product characteristics of the uranium oxide depend greatly on the ways of preparation of the APU , in the present work, the kinetics of deposition and the composition of the formed products upon adding increasing amounts of ammonium hydroxide to uranyl nitrate solution have been followed in a trial to understand the prevailing mechanisms

  17. 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...... the total number of ammonium oxidizing bacteria in the column. © 2013 American Water Works Association AWWA WQTC Conference Proceedings All Rights Reserved.......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 can...

  18. Ammonium first: natural mosses prefer atmospheric ammonium but vary utilization of dissolved organic nitrogen depending on habitat and nitrogen deposition.

    Science.gov (United States)

    Liu, Xue-Yan; Koba, Keisuke; Makabe, Akiko; Li, Xiao-Dong; Yoh, Muneoki; Liu, Cong-Qiang

    2013-07-01

    Mosses, among all types of terrestrial vegetation, are excellent scavengers of anthropogenic nitrogen (N), but their utilization of dissolved organic N (DON) and their reliance on atmospheric N remain uncharacterized in natural environments, which obscures their roles in N cycles. Natural (15) N abundance of N sources (nitrate (NO(3)(-)), ammonium (NH(4)(+)) and DON in deposition and soil) for epilithic and terricolous mosses was analyzed at sites with different N depositions at Guiyang, China. Moss NO(3)(-) assimilation was inhibited substantially by the high supply of NH(4)(+) and DON. Therefore, contributions of NH(4)(+) and DON to moss N were partitioned using isotopic mass-balance methods. The N contributions averaged 56% and 46% from atmospheric NH(4)(+), and 44% and 17% from atmospheric DON in epilithic and terricolous mosses, respectively. In terricolous mosses, soil NH(4)(+) and soil DON accounted for 16% and 21% of bulk N, which are higher than current estimations obtained using (15) N-labeling methods. Moreover, anthropogenic NH(4)(+) deposition suppressed utilization of DON and soil N because of the preference of moss for NH(4)(+) under elevated NH(4)(+) deposition. These results underscore the dominance of, and preference for, atmospheric NH(4)(+) in moss N utilization, and highlight the importance of considering DON and soil N sources when estimating moss N sequestration and the impacts of N deposition on mosses. PMID:23692546

  19. Occurrence of Anaerobic Ammonium Oxidation in the Yangtze Estuary

    Science.gov (United States)

    Hou, L.

    2013-12-01

    Over the past several decades, a large quantity of reactive nitrogen has been transported into the Yangtze estuarine and coastal water, due to intense human activities in the Yangtze River Basin. At present, it annually receives a high load of anthropogenic inorganic nitrogen (about 1.1 × 1011 mol N) from increased agricultural activities, fish farming, and domestic and industrial wastewater discharge in the Yangtze River Basin, consequently leading to severe eutrophication and frequent occurrences of harmful algal blooms in the estuary and adjacent coastal areas. Hence, the microbial nitrogen transformations are of major concern in the Yangtze Estuary. Anaerobic ammonium oxidation (anammox) has been reported to play a significant role in the removal of reactive nitrogen in aquatic ecosystems. In this study, the occurrences of anammox bacteria and associated activity in the Yangtze Estuary were evidenced with molecular and isotope-tracing techniques. It is observed that the anammox bacteria at the study area mainly consisted of Candidatus Scalindua, Brocadia, Kuenenia. Salinity was found to be a key environmental factor controlling distribution and diversity of the anammox bacterial community at the estuarine ecosystem. Also, temperature and organic carbon had significant influences on anammox bacterial biodiversity. Q-PCR assays of anammox bacteria indicated that their abundance had a range of 2.63 ×106 - 9.48 ×107 copies g-1 dry sediment, with high spatiotemporal heterogeneity. The potential anammox activities measured in the present work varied between 0.94 - 6.61nmol N g-1 dry sediment h-1, which were related to temperature, nitrite and anammox bacterial abundance. On the basis of the 15N tracing experiments, the anammox process was estimated to contribute 6.6 - 12.9 % to the total nitrogen loss whereas the remainder was attributed to denitrification.

  20. A strong isotope effect in the phase transition behaviour of ammonium hexachlorotellurate

    International Nuclear Information System (INIS)

    Heat capacity and neutron powder diffraction measurements have been performed on protonated and deuterated ammonium hexachlorotellurate. This powerful combination of techniques has provided a detailed picture of the novel phase transition behaviour in these materials. (orig.)

  1. Heterotrophic ammonium removal characteristics of an aerobic heterotrophic nitrifying-denitrifying bacterium, Providencia rettgeri YL

    Institute of Scientific and Technical Information of China (English)

    TAYLOR Shauna M; HE Yiliang; ZHAO Bin; HUANG Jue

    2009-01-01

    Bacterium Providencia rettgeri YL was found to exhibit an unusual ability to heterotrophically nitrify and aerobically denitrify various concentrations of ammonium (NH4+-N). In order to further analyze its removal ability, several experiments were conducted to identify the growth and ammonium removal response in different carbon to nitrogen (C/N) mass ratios, shaking speeds, temperatures, ammonium concentrations and to qualitatively verify the production of nitrogen gas using gas chromatography techniques. Results showed that under optimum conditions (C/N 10, 30℃, 120 r/min), YL can significantly remove low and high concentrations of ammonium within 12 to 48 h of growth. The nitrification products hydroxylamine (NH2OH), nitrite (NO2-) and nitrate (NO3-) as well as the denitrification product, nitrogen gas (N2), were detected under completely aerobic conditions.

  2. Properties of the Nafion membrane impregnated with hydroxyl ammonium based ionic liquids

    Science.gov (United States)

    Garaev, Valeriy; Kleperis, Janis; Pavlovica, Sanita; Vaivars, Guntars

    2012-08-01

    In this work, the Nafion 112 membrane impregnated with nine various hydroxyl ammonium based ionic liquids have been investigated. The used ionic liquids were combined from hydroxyl ammonium cations (2-hydroxyethylammonium/HEA, bis(2- hydroxyethyl)ammonium/BHEA, tris(2-hydroxyethyl)ammonium/THEA) and carboxylate anions (formate, acetate, lactate). The membranes are characterized by conductivity and thermal stability measurements. It was found, that almost all composites have 10 times higher ion conductivity than a pure Nafion 112 at 90 °C in ambient environment due to the higher thermal stability. The thermal stability of Nafion membrane was increased by all studied nine ionic liquids. In this work, only biodegradable ionic liquids were used for composite preparation.

  3. Antibacterial properties of poly(quaternary ammonium) modified gold and titanium dioxide nanoparticles.

    Science.gov (United States)

    Wan, Weijie; Yeow, John T W

    2012-06-01

    We report excellent antibacterial effect induced by amine-functionalized gold and titanium dioxide nanoparticles without external excitations. The idea originates from the excellent antibacterial property of quaternary ammonium salts. The effects of poly(quaternary ammonium) and polyacrylate sodium functional groups as nanoparticle surfactants are compared to show that poly(quaternary ammonium) functional groups are the main cause of the induced antibacterial effect. 99.999% of E. coli can be destructed in 10 minutes by simply mixing bacteria with nanoparticle dispersions. The effect of nanoparticle concentrations on the antibacterial property is evaluated. Time required to significantly suppress bacteria growth is studied. The result indicates that the excellent antibacterial property can be introduced to any nanomaterials by using poly(quaternary ammonium) functional groups as surfactants. The engineered nanoparticles can find enormous applications such as self-cleaning surfaces, waste water treatment, Lab-on-a-Chip devices and many more. PMID:22905506

  4. Plasmid DNA induces dodecyl triethyl ammonium bromide to aggregate into vesicle

    Institute of Scientific and Technical Information of China (English)

    Xiang Mei Ran; Xia Guo; Jia Tong Ding

    2012-01-01

    Single-chained cationic surfactant dodecyl triethyl ammonium bromide and plasmid DNA together can form vesicles once the concentration of plasmid DNA reaches a critical value (Ccvc).Bigger the size of plasmid DNA,higher the value of Ccvc.

  5. Determination of ammonium in a buddingtonite sample by ion-chromatography

    Science.gov (United States)

    Klock, P.R.; Lamothe, P.J.

    1986-01-01

    An ion-chromatographic method for the direct determination of ammonium, potassium, and sodium in geologic materials is described. Samples are decomposed with a mixture of hydrofluoric and hydrochloric acids in a sealed polycarbonate bottle heated in a microwave oven. The ion-chromatograph separates the cations and determines them by conductivity measurement. The ammonium concentrations thus determined have been verified by use of an ammonia-specific electrode. A total of 32 analyses of ammonium salts by both techniques showed an average error of -4%, with a relative standard deviation (RSD) of 6%. The ammonium concentrations found in a buddingtonite sample had an RSD of 2.2% and their mean agreed with that obtained by the Kjeldahl method. By use of the prescribed dilution of the sample, detection limits of 0.1% can be achieved for all three cations. ?? 1986.

  6. CdTe/ZnS quantum dots as fluorescent probes for ammonium determination.

    Science.gov (United States)

    Yi, Kui-Yu

    2016-06-01

    Novel CdTe/ZnS quantum dot (QD) probes based on the quenching effect were proposed for the simple, rapid, and specific determination of ammonium in aqueous solutions. The QDs were modified using 3-mercaptopropionic acid, and the fluorescence responses of the CdTe/ZnS QD probes to ammonium were detected through regularity quenching. The quenching levels of the CdTe/ZnS QDs and ammonium concentration showed a good linear relationship between 4.0 × 10(-6) and 5.0 × 10(-4) mol/L; the detection limit was 3.0 × 10(-7) mol/L. Ammonium contents in synthetic explosion soil samples were measured to determine the practical applications of the QD probes and a probable quenching mechanism was described. Copyright © 2015 John Wiley & Sons, Ltd. PMID:26542194

  7. Anatase-brookite mixed phase nano TiO2 catalyzed homolytic decomposition of ammonium nitrate.

    Science.gov (United States)

    Vargeese, Anuj A; Muralidharan, Krishnamurthi

    2011-09-15

    Compared to the conventional ammonium perchlorate based solid rocket propellants, burning of ammonium nitrate (AN) based propellants produce environmentally innocuous combustion gases. Application of AN as propellant oxidizer is restricted due to low reactivity and low energetics besides its near room temperature polymorphic phase transition. In the present study, anatase-brookite mixed phase TiO(2) nanoparticles (~ 10 nm) are synthesized and used as catalyst to enhance the reactivity of the environmental friendly propellant oxidizer ammonium nitrate. The activation energy required for the decomposition reactions, computed by differential and non-linear integral isoconversional methods are used to establish the catalytic activity. Presumably, the removal of NH(3) and H(2)O, known inhibitors of ammonium nitrate decomposition reaction, due to the surface reactions on active surface of TiO(2) changes the decomposition pathway and thereby the reactivity.

  8. Treatment of ammonium-rich swine waste in modified porphyritic andesite fixed-bed anaerobic bioreactor.

    Science.gov (United States)

    Wang, Qinghong; Yang, Yingnan; Li, Dawei; Feng, Chuanping; Zhang, Zhenya

    2012-05-01

    In this study, a modified porphyritic andesite (WRS) was developed as ammonium adsorbent and bed material for the anaerobic digestion of ammonium-rich swine waste. The performance in bioreactors with modified WRS, natural WRS, calcium chloride and no additives was investigated. The bioreactor with modified WRS exhibited the best performance, with start-up time on the 7th day, methane yield of 359.71 ml/g-VS, and COD removal of 67.99% during all 44 days of the experiment at 35°C. The effective ammonium adsorption and essential ions dissociation for microorganisms by modified WRS, as well as the immobilization of microbial on the surface of the modified WRS play a great role on the high efficiency anaerobic digestion of ammonium-rich swine waste. PMID:22366608

  9. Evaluation of chitosan quaternary ammonium salt-modified resin denture base material.

    Science.gov (United States)

    Song, Rong; Zhong, Zhaohua; Lin, Lexun

    2016-04-01

    Chitosan quaternary ammonium salt displays good antioxidant and antibacterial characteristics and it shows appreciable solubility in water. When added to the traditional denture material to form a resin base, it could promote good oral health by improving the oral environment. In this study, chitosan quaternary ammonium salt was added to the denture material following two different methods. After three months of immersion in artificial saliva, the specimens were tested for tensile strength and were scanned by electron microscope. The murine fibroblast cytotoxicity and antibacterial properties were also tested. The result showed no significant differences in the tensile strength and in the proliferation of murine L929 fibroblast cells. The two structures of chitosan quaternary ammonium salt-modified denture material had different degrees of corrosion resistance and antimicrobial properties. These results indicate that chitosan quaternary ammonium salt-modified resin denture base material has the potential to become a new generation oral denture composite material.

  10. The anomalous solid state decomposition of ammonium dinitramide: a matter of surface polarization.

    Science.gov (United States)

    Rahm, Martin; Brinck, Tore

    2009-05-28

    Polarized dinitramide anions on the surface of solid ammonium dinitramide (ADN) have a decomposition barrier that is reduced by 16 kcal mol(-1) and explain the anomalous solid state decomposition of ADN. PMID:19436902

  11. Interaction between Ammonium Toxicity and Green Tide Development Over Seagrass Meadows

    DEFF Research Database (Denmark)

    Marin, Francisco Moreno; Vergara, Juan J.; Pérez-Llorens, J. Lucas;

    2016-01-01

    Eutrophication affects seagrasses negatively by increasing light attenuation through stimulation of biomass of fast-growing, bloom-forming algae and because high concentrations of ammonium in the water can be toxic to higher plants. We hypothesized nevertheless, that moderate amounts of nitrophilic...... macroalgae that coexists with seagrasses under eutrophic conditions, can alleviate the harmful effects of eutrophication on seagrasses by reducing ammonium concentrations in the seawater to non-toxic levels because such algae have a very large capacity to take up inorganic nutrients. We studied therefore how...... combinations of different ammonium concentrations (0, 25 and 50 μM) and different standing stocks of macroalgae (i.e. 0, 1 and 6 layers of Ulva sp.) affected survival, growth and net production of the seagrass Zostera noltei. In the absence of Ulva sp., increasing ammonium concentrations had a negative...

  12. Crystal structure of cyclo­hexyl­ammonium thio­cyanate

    OpenAIRE

    Abdulaziz A. Bagabas; Sultan B. Alhoshan; Hazem A. Ghabbour; C S Chidan Kumar; Fun, Hoong-Kun

    2015-01-01

    In the title salt, C6H11NH3 +·SCN−, the cyclo­hexyl­ammonium ring adopts a slightly distorted chair conformation. The ammonium group occupies an equatorial position to minimize 1,3 and 1,5 diaxial inter­actions. In the crystal, the components are linked by N—H⋯N and N—H⋯S hydrogen-bonding inter­actions, resulting in a three-dimensional network.

  13. 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. PMID:19850316

  14. Reduction of formaldehyde concentrations in the air and cadaveric tissues by ammonium carbonate

    OpenAIRE

    Kawamata, Seiichi; Kodera, Haruo

    2004-01-01

    The reduction of formaldehyde by ammonium carbonate was examined in cadavers and in vitro. Formaldehyde concentrations in the air (10 cm above human cadavers) and in various cadaveric tissues were measured with or without perfusion of ammonium carbonate solution into formaldehyde-fixed cadavers. Air samples were monitored using Kitagawa gas detector tubes. For measurement of formaldehyde in tissues, muscles and organs were cut into small pieces and tissue fluids were separated out by centrifu...

  15. Synthesis of Main-Chain Chiral Quaternary Ammonium Polymers for Asymmetric Catalysis Using Quaternization Polymerization

    Directory of Open Access Journals (Sweden)

    Md. Masud Parvez

    2012-06-01

    Full Text Available Main-chain chiral quaternary ammonium polymers were successfully synthesized by the quaternization polymerization of cinchonidine dimer with dihalides. The polymerization occurred smoothly under optimized conditions to give novel type of main-chain chiral quaternary ammonium polymers. The catalytic activity of the polymeric chiral organocatalysts was investigated on the asymmetric benzylation of N-(diphenylmethylideneglycine tert-butyl ester.

  16. The Basis of Ammonium Release in nifL Mutants of Azotobacter vinelandii

    OpenAIRE

    Brewin, Brett; Woodley, Paul; DRUMMOND, MARTIN

    1999-01-01

    In Azotobacter vinelandii, nitrogen fixation is regulated at the transcriptional level by an unusual two-component system encoded by nifLA. Certain mutations in nifL result in the bacterium releasing large quantities of ammonium into the medium, and earlier work suggested that this occurs by a mechanism that does not involve NifA, the activator of nif gene transcription. We have investigated a number of possible alternative mechanisms and find no evidence for their involvement in ammonium rel...

  17. Synthesis and applications of novel bis(ammonium) chiral ionic liquids derived from isomannide

    DEFF Research Database (Denmark)

    Kumar, Vineet; Olsen, Carl Erik; Schäffer, Susan J.;

    2007-01-01

    Carbohydrate-based novel bis(ammonium) chiral ionic liquids have been synthesized by following a straightforward protocol using isomannide as the substrate. Their applications in chiral discrimination and optical resolution of racemates have been established.......Carbohydrate-based novel bis(ammonium) chiral ionic liquids have been synthesized by following a straightforward protocol using isomannide as the substrate. Their applications in chiral discrimination and optical resolution of racemates have been established....

  18. The Effect of the Ammonium Group on the Different Annealing Processes

    International Nuclear Information System (INIS)

    The ammonium group can play an essential role in the different annealing processes of neutron-irradiated ammonium compounds. Some details of this effect were investigated. To give a more complete picture of this subject first some typical results, already published, are briefly discussed, concerning the thermal, radiation, photochemical and ultra-sonic annealing of ammonium and potassium sulphate as well as of ammonium and potassium dichromate. Afterwards new experimental data are reported showing the influence of the ammonium group on the thermal, radiation and ultra-sonic annealing of mono-, di- and triammonium phosphates. It was established that under the conditions of neutron irradiation in the pile the ammonium group in a compound can be transformed into certain metastabile recoil fragments, which can lead to the formation of reducing substances, e. g. hydrazine. The yield of hydrazine increases by the subsequent treatment of the neutron-irradiated solid samples with gamma-rays, ultra sound etc. Simultaneously with the increase in the hydrazine yield a strong change of the retention occurs. (author)

  19. Floc flotation of jamesonite fines in aqueous suspensions induced by ammonium dibutyl dithiophosphate

    Institute of Scientific and Technical Information of China (English)

    张婷; 覃文庆

    2015-01-01

    The hydrophobic flocculation of jamesonite fines in aqueous suspensions induced by ammonium dibutyl dithiophosphate was investigated using laser particle size analysis, microscope analysis, electrophoretic light scattering and infrared spectroscopy. Single minerals of 4.607 µm for the 50% volumetric diameters were researched by varying several parameters, including pH, ammonium dibutyl dithiophosphate concentration, stirring strength and kerosene addition. It is found that the maximal floatability of jamesonite fines is induced by ammonium dibutyl dithiophosphate at pH 6, and the floc flotation increases with increasing ammonium dibutyl dithiophosphate concentration despite a simultaneous increase in the negativeζpotential of jamesonite, meaning that hydrophobic interaction between the particles increases much more strongly than electric double layer repulsion from the adsorption of ammonium dibutyl dithiophosphate. It is also found that the floc flotation is closely correlated with the size of flocs, which is strongly influenced by the stirring strength and enhanced by the addition of a small amount of kerosene. The results of FTIR spectra indicate that adsorption of ammonium dibutyl dithiophosphate onto jamesonite is chemical adsorption and the adsorption product is lead dibutyl dithiophosphate.

  20. The basis of ammonium release in nifL mutants of Azotobacter vinelandii.

    Science.gov (United States)

    Brewin, B; Woodley, P; Drummond, M

    1999-12-01

    In Azotobacter vinelandii, nitrogen fixation is regulated at the transcriptional level by an unusual two-component system encoded by nifLA. Certain mutations in nifL result in the bacterium releasing large quantities of ammonium into the medium, and earlier work suggested that this occurs by a mechanism that does not involve NifA, the activator of nif gene transcription. We have investigated a number of possible alternative mechanisms and find no evidence for their involvement in ammonium release. Enhancement of NifA-mediated transcription, on the other hand, by either elimination of nifL or overexpression of nifA, resulted in ammonium release, correlating with enhanced levels of nifH mRNA, raised levels of nitrogenase and acetylene-reducing activity, and increased concentrations of intracellular ammonium. Up to 35 mM ammonium can accumulate in the medium. Where measured, intracellular levels exceeded extracellular levels, indicating that rather than being actively transported, ammonium is lost from the cell passively, possibly by reversal of an NH(4)(+) uptake system. The data also indicate that in the wild type the bulk of NifA is inactivated by NifL during steady-state growth on dinitrogen. PMID:10572141

  1. Application of Neesler reagent in the ammonium quantification used in the fermentations of biotechnology products

    Directory of Open Access Journals (Sweden)

    Dinorah Torres-Idavoy

    2015-08-01

    Full Text Available The ammonium salts are used in fermentations to supplement the deficient amounts of nitrogen and stabilize the pH of the culture medium. The excess ammonium ion exerts a detrimental effect on the fermentation process inhibiting microbial growth. An analytical method based on Neesler reagent was developed for monitoring and controlling the concentration of ammonium during the fermentation process. The test was standardized, by means of the selection of measuring equipment, and the reaction time as well as comparing standards of ammonium salts. The method was characterized with the evaluation of the next parameters: Specificity, Linearity and Range, Quantification Limit, Accuracy and Precision. The method proved to be specific. Two linear curves were defined in the ranges of concentrations of ammonium chloride salt (2-20 μg/ml and ammonium sulfate salt (5-30 μg/ml. The limits of quantification were the lowest points of each one. The method proved to be accurate and precise. This assay was applied to samples of the yeast culture and bacteria of the genus Saccharomyces and E. coli respectively. A novel method in micro plate for quantification and analytical control of ammonia was developed. This method is used to control this fundamental chemical component in the fermentations, to optimize the culture medium. Thus, an appropriate expression of recombinant proteins and proper vaccine candidates for clinical use are achieved

  2. Improving the Sensitivity of Matrix-Assisted Ionization (MAI) Mass Spectrometry Using Ammonium Salts.

    Science.gov (United States)

    Chubatyi, Nicholas D; McEwen, Charles N

    2015-10-01

    In matrix-assisted ionization (MAI), analyte incorporated in a small molecule matrix is introduced into an aperture linking atmospheric pressure with the vacuum of a mass spectrometer. Gas-phase analyte ions are spontaneously produced without use of a laser or high voltage. Here we investigate analyte and background ion abundances upon addition of ammonium salts to various MAI matrix/analyte solutions. Regardless of the ammonium salt or matrix used, chemical background ions are suppressed and/or analyte ion abundance improved for basic small molecules, peptides, and proteins. Background ion abundances increase with increasing inlet temperature, but are suppressed with addition of any of a variety of ammonium salts without much effect on the total ion abundances of the analyte ions. However, at lower inlet temperature using the matrices 2-bromo-2-nitropropane-1,3-diol, 1,2-dicyanobenzene, and 3-nitrobenzonitrile (3-NBN), analyte ion abundance increases and any chemical background decreases upon addition of ammonium salt. The improvement in sensitivity using 3-NBN with ammonium salt allows full acquisition mass spectra consuming as little as 1 fmol of ubiquitin. More complete peptide coverage for 100 fmol of a BSA tryptic digest, and increased sensitivity of drugs spiked in urine and saliva were observed after ammonium salt addition to the 3-NBN matrix. PMID:26122522

  3. Depositional ice nucleation on solid ammonium sulfate and glutaric acid particles

    Directory of Open Access Journals (Sweden)

    K. J. Baustian

    2010-03-01

    Full Text Available Heterogeneous ice nucleation on solid ammonium sulfate and glutaric acid particles was studied using optical microscopy and Raman spectroscopy. Optical microscopy was used to detect selective nucleation events as water vapor was slowly introduced into an environmental sample cell. Particles that nucleated ice were dried via sublimation and examined in detail using Raman spectroscopy. Depositional ice nucleation is highly selective and occurred preferentially on just a few ammonium sulfate and glutaric acid particles in each sample. For freezing temperatures between 214 K and 235 K an average ice saturation ratio of S = 1.10±0.07 for solid ammonium sulfate was observed. Over the same temperature range, S values observed for ice nucleation on glutaric acid particles increased from 1.2 at 235 K to 1.6 at 218 K. Experiments with externally mixed particles further show that ammonium sulfate is a more potent ice nucleus than glutaric acid. Our results suggest that heterogeneous nucleation on ammonium sulfate may be an important pathway for atmospheric ice nucleation and cirrus cloud formation when solid ammonium sulfate aerosol particles are available for ice formation. This pathway for ice formation may be particularly significant near the tropical tropopause region where sulfates are abundant and other species known to be good ice nuclei are depleted.

  4. High Pressure Burn Rate Measurements on an Ammonium Perchlorate Propellant

    Energy Technology Data Exchange (ETDEWEB)

    Glascoe, E A; Tan, N

    2010-04-21

    High pressure deflagration rate measurements of a unique ammonium perchlorate (AP) based propellant are required to design the base burn motor for a Raytheon weapon system. The results of these deflagration rate measurements will be key in assessing safety and performance of the system. In particular, the system may experience transient pressures on the order of 100's of MPa (10's kPSI). Previous studies on similar AP based materials demonstrate that low pressure (e.g. P < 10 MPa or 1500 PSI) burn rates can be quite different than the elevated pressure deflagration rate measurements (see References and HPP results discussed herein), hence elevated pressure measurements are necessary in order understand the deflagration behavior under relevant conditions. Previous work on explosives have shown that at 100's of MPa some explosives will transition from a laminar burn mechanism to a convective burn mechanism in a process termed deconsolidative burning. The resulting burn rates that are orders-of-magnitude faster than the laminar burn rates. Materials that transition to the deconsolidative-convective burn mechanism at elevated pressures have been shown to be considerably more violent in confined heating experiments (i.e. cook-off scenarios). The mechanisms of propellant and explosive deflagration are extremely complex and include both chemical, and mechanical processes, hence predicting the behavior and rate of a novel material or formulation is difficult if not impossible. In this work, the AP/HTPB based material, TAL-1503 (B-2049), was burned in a constant volume apparatus in argon up to 300 MPa (ca. 44 kPSI). The burn rate and pressure were measured in-situ and used to calculate a pressure dependent burn rate. In general, the material appears to burn in a laminar fashion at these elevated pressures. The experiment was reproduced multiple times and the burn rate law using the best data is B = (0.6 {+-} 0.1) x P{sup (1.05{+-}0.02)} where B is the burn

  5. Differences in the reactivity of ammonium salts with methylamine

    Directory of Open Access Journals (Sweden)

    Y. Liu

    2012-06-01

    Full Text Available The heterogeneous uptake of methylamine (MA onto (NH42SO4, NH4HSO4, NH4NO3 and NH4Cl was investigated using a Knudsen cell reactor coupled to a quadrupole mass spectrometer, in situ Raman spectrometer and theoretical calculations. Exchange reactions were observed between MA and NH4NO3, (NH42SO4, and NH4Cl were observed at 298 K. Simple acid-base reaction for MA was found taking place on NH4HSO4. CH3NH3NO3 and CH3NH3Cl are not stable at low pressure and have higher dissociation vapor pressure than methylammonium sulfate. The observed uptake coefficients of MA on (NH42SO4, NH4HSO4, NH4NO3 and NH4Cl at 298 K were measured to be 6.30±1.03×10−3, 1.78±0.36×10−2, 8.79±1.99×10−3 and 2.29±0.28×10−3, respectively. A linear free energy relationship was found for the heterogeneous reactions between MA and NH4Cl, (NH42SO4 and NH4NO3. Namely, the natural logarithm of uptake coefficients of MA on these ammonium salts is linearly related to the electrostatic potential of the H atom in the NH4+ group.

  6. Nutrient release and ammonium sorption by poultry litter and wood biochars in stormwater treatment.

    Science.gov (United States)

    Tian, Jing; Miller, Valentina; Chiu, Pei C; Maresca, Julia A; Guo, Mingxin; Imhoff, Paul T

    2016-05-15

    The feasibility of using biochar as a filter medium in stormwater treatment facilities was evaluated with a focus on ammonium retention. Successive batch extractions and batch ammonium sorption experiments were conducted in both deionized (DI) water and artificial stormwater using poultry litter (PL) and hardwood (HW) biochars pyrolyzed at 400°C and 500°C. No measureable nitrogen leached from HW biochars except 0.07 μmol/g of org-N from 400°C HW biochar. PL biochar pyrolyzed at 400°C leached 120-127 μmol/g of nitrogen but only 7.1-8.6 μmol/g of nitrogen when pyrolyzed at 500°C. Ammonium sorption was significant for all biochars. At a typical ammonium concentration of 2mg/L in stormwater, the maximum sorption was 150 mg/kg for PL biochar pryolyzed at 400°C. In stormwater, ion competition (e.g. Ca(2+)) suppressed ammonium sorption compared to DI water. Surprisingly, ammonium sorption was negatively correlated to the BET surface area of the tested biochars, but increased linearly with cation exchange capacity. Cation exchange capacity was the primary mechanism controlling ammonium sorption and was enhanced by pyrolysis at 400°C, while BET surface area was enhanced by pyrolysis at 500°C. The optimal properties (BET surface area, CEC, etc.) of biochar as a sorbent are not fixed but depend on the target pollutant. Stormwater infiltration column experiments in sand with 10% biochar removed over 90% of ammonium with influent ammonium concentration of 2mg/L, compared to only 1.7% removal in a sand-only column, indicating that kinetic limitations on sorption were minor for the storm conditions studied. Hardwood and poultry litter biochar pyrolyzed at 500°C and presumably higher temperature may be viable filter media for stormwater treatment facilities, as they showed limited release of organic and inorganic nutrients and acceptable ammonium sorption. PMID:26938322

  7. Thermal stability and kinetics of decomposition of ammonium nitrate in the presence of pyrite.

    Science.gov (United States)

    Gunawan, Richard; Zhang, Dongke

    2009-06-15

    The interaction between ammonium nitrate based industrial explosives and pyrite-rich minerals in mining operations can lead to the occurrence of spontaneous explosion of the explosives. In an effort to provide a scientific basis for safe applications of industrial explosives in reactive mining grounds containing pyrite, ammonium nitrate decomposition, with and without the presence of pyrite, was studied using a simultaneous Differential Scanning Calorimetry and Thermogravimetric Analyser (DSC-TGA) and a gas-sealed isothermal reactor, respectively. The activation energy and the pre-exponential factor of ammonium nitrate decomposition were determined to be 102.6 kJ mol(-1) and 4.55 x 10(7)s(-1) without the presence of pyrite and 101.8 kJ mol(-1) and 2.57 x 10(9)s(-1) with the presence of pyrite. The kinetics of ammonium nitrate decomposition was then used to calculate the critical temperatures for ammonium nitrate decomposition with and without the presence of pyrite, based on the Frank-Kamenetskii model of thermal explosion. It was shown that the presence of pyrite reduces the temperature for, and accelerates the rate of, decomposition of ammonium nitrate. It was further shown that pyrite can significantly reduce the critical temperature of ammonium nitrate decomposition, causing undesired premature detonation of the explosives. The critical temperature also decreases with increasing diameter of the blast holes charged with the explosive. The concept of using the critical temperature as indication of the thermal stability of the explosives to evaluate the risk of spontaneous explosion was verified in the gas-sealed isothermal reactor experiments. PMID:19056177

  8. N-Chlorotaurine and ammonium chloride: an antiseptic preparation with strong bactericidal activity.

    Science.gov (United States)

    Gottardi, Waldemar; Arnitz, Roland; Nagl, Markus

    2007-04-20

    The bactericidal activity of the endogenous antiseptic N-chlorotaurine (NCT) is significantly enhanced in the presence of ammonium chloride which induces the formation of monochloramine (NH(2)Cl) whose strong bactericidal activity is well known. In this study the properties of NCT plus ammonium chloride have been investigated. The reaction of active chlorine compounds like chloramine-T (N-chlorotoluene-sulfonamide sodium), chloroisocyanuric acid derivatives, hypochlorites (NaOCl, CaOCl(2)) with ammonium chloride did not stop at the stage of monochloramine, and the pungent smelling by-products di- and trichloramine, NHCl(2) and NCl(3), were also formed. This was not the case with NCT where only monochloramine was generated. The equilibrium constant of the reaction of NCT with ammonium was found to be [Formula: see text] , which allows to estimate the equilibrium concentration of monochloramine in aqueous solutions of NCT and ammonium chloride. At concentrations each ranging between 0.01% and 1.0% it comes to [NH(2)Cl]=3.5-254 ppm. As an unexpected result the monochloramine containing formulation turned out to be most stable in plain water without buffer additives. Quantitative killing assays revealed complete inactivation of 10(6) to 10(7)CFU/mL of seven bacterial strains by 0.1% NCT plus 0.1% ammonium chloride within 5 min, while with plain 0.1% NCT an incubation time of 2-4h was needed to achieve the same effect. The highly significant increase of bactericidal activity (200-300-fold) could be assigned to the presence of monochloramine which could be isolated by vacuum distillation. Aqueous solutions of NCT and ammonium chloride provide a highly effective and well tolerable antiseptic preparation appropriate to a treatment cycle of at least 1 month if stored in the refrigerator.

  9. Thermal stability and kinetics of decomposition of ammonium nitrate in the presence of pyrite

    Energy Technology Data Exchange (ETDEWEB)

    Gunawan, Richard, E-mail: R.Gunawan@curtin.edu.au [Centre for Fuels and Energy, Curtin University of Technology, G.P.O. Box U1987, Perth, WA 6845 (Australia); Zhang Dongke [Centre for Petroleum, Fuels and Energy, School of Mechanical Engineering (M050), University of Western Australia, 35 Stirling Highway, Crawley WA 6009 (Australia)

    2009-06-15

    The interaction between ammonium nitrate based industrial explosives and pyrite-rich minerals in mining operations can lead to the occurrence of spontaneous explosion of the explosives. In an effort to provide a scientific basis for safe applications of industrial explosives in reactive mining grounds containing pyrite, ammonium nitrate decomposition, with and without the presence of pyrite, was studied using a simultaneous Differential Scanning Calorimetry and Thermogravimetric Analyser (DSC-TGA) and a gas-sealed isothermal reactor, respectively. The activation energy and the pre-exponential factor of ammonium nitrate decomposition were determined to be 102.6 kJ mol{sup -1} and 4.55 x 10{sup 7} s{sup -1} without the presence of pyrite and 101.8 kJ mol{sup -1} and 2.57 x 10{sup 9} s{sup -1} with the presence of pyrite. The kinetics of ammonium nitrate decomposition was then used to calculate the critical temperatures for ammonium nitrate decomposition with and without the presence of pyrite, based on the Frank-Kamenetskii model of thermal explosion. It was shown that the presence of pyrite reduces the temperature for, and accelerates the rate of, decomposition of ammonium nitrate. It was further shown that pyrite can significantly reduce the critical temperature of ammonium nitrate decomposition, causing undesired premature detonation of the explosives. The critical temperature also decreases with increasing diameter of the blast holes charged with the explosive. The concept of using the critical temperature as indication of the thermal stability of the explosives to evaluate the risk of spontaneous explosion was verified in the gas-sealed isothermal reactor experiments.

  10. Root ABA Accumulation Enhances Rice Seedling Drought Tolerance under Ammonium Supply: Interaction with Aquaporins.

    Science.gov (United States)

    Ding, Lei; Li, Yingrui; Wang, Ying; Gao, Limin; Wang, Min; Chaumont, François; Shen, Qirong; Guo, Shiwei

    2016-01-01

    In previous studies, we demonstrated that ammonium nutrition enhances the drought tolerance of rice seedlings compared to nitrate nutrition and contributes to a higher root water uptake ability. It remains unclear why rice seedlings maintain a higher water uptake ability when supplied with ammonium under drought stress. Here, we focused on the effects of nitrogen form and drought stress on root abscisic acid (ABA) concentration and aquaporin expression using hydroponics experiments and stimulating drought stress with 10% PEG6000. Drought stress decreased the leaf photosynthetic rate and stomatal conductivity and increased the leaf temperature of plants supplied with either ammonium or nitrate, but especially under nitrate supply. After 4 h of PEG treatment, the root protoplast water permeability and the expression of root PIP and TIP genes decreased in plants supplied with ammonium or nitrate. After 24 h of PEG treatment, the root hydraulic conductivity, the protoplast water permeability, and the expression of some aquaporin genes increased in plants supplied with ammonium compared to those under non-PEG treatment. Root ABA accumulation was induced by 24 h of PEG treatment, especially in plants supplied with ammonium. The addition of exogenous ABA decreased the expression of PIP and TIP genes under non-PEG treatment but increased the expression of some of them under PEG treatment. We concluded that drought stress induced a down-regulation of aquaporin expression, which appeared earlier than did root ABA accumulation. With continued drought stress, aquaporin expression and activity increased due to root ABA accumulation in plants supplied with ammonium. PMID:27559341

  11. Root ABA Accumulation Enhances Rice Seedling Drought Tolerance under Ammonium Supply: Interaction with Aquaporins

    Science.gov (United States)

    Ding, Lei; Li, Yingrui; Wang, Ying; Gao, Limin; Wang, Min; Chaumont, François; Shen, Qirong; Guo, Shiwei

    2016-01-01

    In previous studies, we demonstrated that ammonium nutrition enhances the drought tolerance of rice seedlings compared to nitrate nutrition and contributes to a higher root water uptake ability. It remains unclear why rice seedlings maintain a higher water uptake ability when supplied with ammonium under drought stress. Here, we focused on the effects of nitrogen form and drought stress on root abscisic acid (ABA) concentration and aquaporin expression using hydroponics experiments and stimulating drought stress with 10% PEG6000. Drought stress decreased the leaf photosynthetic rate and stomatal conductivity and increased the leaf temperature of plants supplied with either ammonium or nitrate, but especially under nitrate supply. After 4 h of PEG treatment, the root protoplast water permeability and the expression of root PIP and TIP genes decreased in plants supplied with ammonium or nitrate. After 24 h of PEG treatment, the root hydraulic conductivity, the protoplast water permeability, and the expression of some aquaporin genes increased in plants supplied with ammonium compared to those under non-PEG treatment. Root ABA accumulation was induced by 24 h of PEG treatment, especially in plants supplied with ammonium. The addition of exogenous ABA decreased the expression of PIP and TIP genes under non-PEG treatment but increased the expression of some of them under PEG treatment. We concluded that drought stress induced a down-regulation of aquaporin expression, which appeared earlier than did root ABA accumulation. With continued drought stress, aquaporin expression and activity increased due to root ABA accumulation in plants supplied with ammonium. PMID:27559341

  12. Investigation of bimetallic thiocyanates belonging to ABTC structure type: ZnCd(SCN){sub 4} and AHg(SCN){sub 4} (A = Zn, Cd, Mn) as nonlinear optical crystal materials

    Energy Technology Data Exchange (ETDEWEB)

    Wang, X.-Q.; Xu, D.; Lue, M.-K.; Yuan, D.-R.; Zhang, G.-H.; Meng, F.-Q.; Guo, S.-Y.; Zhou, M.; Liu, J.-R. [Shandong Univ. (China). State Key Lab. of Crystal Materials; Li, X.-R. [Shandong Securities Ltd. Co., SD (China)

    2001-07-01

    Bimetallic thiocyanate complexes crystal materials belonging to ABTC structure type: ZnCd(SCN){sub 4} and AHg(SCN){sub 4} (A = Zn, Cd, Mn) which are potentially useful in second harmonic generation (SHG) have been prepared. Their structural, optical and physicochemical properties are characterized by infrared spectroscopy, X-ray powder diffraction, vis/UV/NIR spectroscopy, SHG measurements and thermal analysis. The states of crystal growth solutions are discussed in this article. The crystals belong to tetragonal system with the space group I anti 4 and exhibit SHG efficiencies over one order of magnitude higher than that of Urea. Their transparency cutoffs lie in the UV region, and they possess good physicochemical stabilities. (orig.)

  13. Higher Ammonium Transamination Capacity Can Alleviate Glutamate Inhibition on Winter Wheat (Triticum aestivum L.) Root Growth under High Ammonium Stress.

    Science.gov (United States)

    Wang, Feng; Gao, Jingwen; Liu, Yang; Tian, Zhongwei; Muhammad, Abid; Zhang, Yixuan; Jiang, Dong; Cao, Weixing; Dai, Tingbo

    2016-01-01

    Most of the studies about NH4+ stress mechanism simply address the effects of free NH4+, failing to recognize the changed nitrogen assimilation products. The objective of this study was to elucidate the effects of glutamate on root growth under high ammonium (NH4+) conditions in winter wheat (Triticum aestivum L.). Hydroponic experiments were conducted using two wheat cultivars, AK58 (NH4+-sensitive) and Xumai25 (NH4+-tolerant) with either 5 mM NH4+ nitrogen (AN) as stress treatment or 5 mM nitrate (NO3-) nitrogen as control. To evaluate the effects of NH4+-assimilation products on plant growth, 1 μM L-methionine sulfoximine (MSO) (an inhibitor of glutamine synthetase (GS)) and 1 mM glutamates (a primary N assimilation product) were added to the solutions, respectively. The AN significantly reduced plant biomass, total root length, surface area and root volume in both cultivars, but less effect was observed in Xumai25. The inhibition effects were alleviated by the application of MSO but strengthened by the application of glutamate. The AN increased the activities of GS, glutamate dehydrogenase (GDH) in both cultivars, resulting in higher glutamate contents. However, its contents were decreased by the application of MSO. Compared to AK58, Xumai25 showed lower glutamate contents due to its higher activities of glutamic-oxaloacetic transaminase (GOT) and glutamic-pyruvic transaminase (GPT). With the indole-3-acetic acid (IAA) contents decreasing in roots, the ratio of shoot to root in IAA was increased, and further increased by the application of glutamate, and reduced by the application of MSO, but the ratio was lower in Xumai25. Meanwhile, the total soluble sugar contents and its root to shoot ratio also showed similar trends. These results indicate that the NH4+-tolerant cultivar has a greater transamination ability to prevent glutamate over-accumulation to maintain higher IAA transport ability, and consequently promoted soluble sugar transport to roots, further

  14. Impact of Ammonium on Syntrophic Organohalide-Respiring and Fermenting Microbial Communities.

    Science.gov (United States)

    Delgado, Anca G; Fajardo-Williams, Devyn; Kegerreis, Kylie L; Parameswaran, Prathap; Krajmalnik-Brown, Rosa

    2016-01-01

    Syntrophic interactions between organohalide-respiring and fermentative microorganisms are critical for effective bioremediation of halogenated compounds. This work investigated the effect of ammonium concentration (up to 4 g liter(-1) NH4 (+)-N) on trichloroethene-reducing Dehalococcoides mccartyi and Geobacteraceae in microbial communities fed lactate and methanol. We found that production of ethene by D. mccartyi occurred in mineral medium containing ≤2 g liter(-1) NH4 (+)-N and in landfill leachate. For the partial reduction of trichloroethene (TCE) to cis-dichloroethene (cis-DCE) at ≥1 g liter(-1) NH4 (+)-N, organohalide-respiring dynamics shifted from D. mccartyi and Geobacteraceae to mainly D. mccartyi. An increasing concentration of ammonium was coupled to lower metabolic rates, longer lag times, and lower gene abundances for all microbial processes studied. The methanol fermentation pathway to acetate and H2 was conserved, regardless of the ammonium concentration provided. However, lactate fermentation shifted from propionic to acetogenic at concentrations of ≥2 g liter(-1) NH4 (+)-N. Our study findings strongly support a tolerance of D. mccartyi to high ammonium concentrations, highlighting the feasibility of organohalide respiration in ammonium-contaminated subsurface environments. IMPORTANCE Contamination with ammonium and chlorinated solvents has been reported in numerous subsurface environments, and these chemicals bring significant challenges for in situ bioremediation. Dehalococcoides mccartyi is able to reduce the chlorinated solvent trichloroethene to the nontoxic end product ethene. Fermentative bacteria are of central importance for organohalide respiration and bioremediation to provide D. mccartyi with H2, their electron donor, acetate, their carbon source, and other micronutrients. In this study, we found that high concentrations of ammonium negatively correlated with rates of trichloroethene reductive dehalogenation and

  15. Alternative process to produce UF{sub 4} using the effluent from ammonium uranyl carbonate route

    Energy Technology Data Exchange (ETDEWEB)

    Silva Neto, Joao B.; Garcia, Rafael Henrique Lazzari; Dal Vechio, Edvaldo, E-mail: jbsneto@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), SP (Brazil); Riella, Humberto G., E-mail: riella@enq.ufsc.br [Universidade Federal de Santa Catarina (UFSC), Florianopolis, SC (Brazil); Instituto Nacional de Ciencias e Tecnologia de Reatores Nucleares Inovadores (INCT/CNPq) (Brazil); Carvalho, Elita F. Urano de; Durazzo, Michelangelo [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), SP (Brazil); Instituto Nacional de Ciencias e Tecnologia de Reatores Nucleares Inovadores (INCT/CNPq) (Brazil)

    2011-07-01

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

  16. 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. PMID:20669719

  17. Evaluation of quaternary ammonium halides for removal of methyl iodide from flowing air streams

    International Nuclear Information System (INIS)

    The quaternary ammonium halides of several tertiary amines were used as impregnants on activated carbon and were tested for methyl iodide penetration in accordance with test Method A, ASTM D3803, 1979, ''Standard Test Methods for Radio-iodine Testing of Nuclear Grade Gas Phase Adsorbents''. The results suggest that the primary removal mechanism for methyl iodide-131 is isotopic exchange with the quaternary ammonium halide. For example, a 5 wt% impregnation of each of the tetramethyl, tetraethyl, tetrapropyl and tetrabutyl ammonium iodides on activated carbon yielded percent penetrations of 0.47, 0.53, 0.78, and 0.08 respectively when tested according to Method A of ASTM D3803. A sample impregnated with 5% tetramethyl ammonium hydroxide gave a methyl iodide penetration of 64.87%, thus supporting the isotopic exchange mechanism for removal. It has been a generally held belief that the success of tertiary amines as impregnants for radioiodine removal is a result of their ability to complex with the methyl iodide. The results of the work indicates that the superiority of the tertiary amines similar to triethylene diamine and quinuclidine, when compared to their straight chain analogs, is a result of their ease in reacting with methyl iodide-127 to form the quaternary ammonium iodide followed by isotopic exchange

  18. Origins of the subsurface ammonium maximum in the Southeast Bering Sea

    Science.gov (United States)

    Mordy, Calvin W.; Stabeno, Phyllis J.; Righi, Dylan; Menzia, Frederick A.

    2008-08-01

    In the Bering Sea, it has long been argued that ammonium-rich bottom water from the middle shelf of Bristol Bay is tidally diffused seaward resulting in a mid-depth ammonium tongue over the outer shelf. Weak horizontal mean flows in the region (relative to an especially strong tidal component) support this contention. We examined the distribution of ammonium further north in the vicinity of the Pribilof Islands. On the middle shelf, bottom waters had concentrations of 4-7 μmol kg -1, and over the outer shelf there was a mid-depth ammonium tongue. Optimal multiparameter analysis of hydrographic data suggested that bottom waters from the middle shelf were prevalent across the outer shelf, and could account for this ammonium tongue. Drifter tracks demonstrated that middle shelf water was incorporated into a westward flow along the shelf break south of St. George Island, and mean flows derived from several decades of drifter tracks also show prominent cross-shelf advection in the region. This was consistent with a scalar argument suggesting that, in the vicinity of the Pribilof Islands, the seaward movement of middle shelf water, and loss of nitrogen over the middle shelf, was the result of advection rather than tidally driven lateral diffusion.

  19. Nitrogen (15N) recovery from ammonium and nitrate applied to the soil by sugar cane

    International Nuclear Information System (INIS)

    An experiment was developed in a field aimed to compare the recovery of the ammonium-15 N and nitrate-15 N by the sugar cane plants harvested mechanically without burning. A rate of 70 kg ha-1 of N was applied as ammonium nitrate, in strip, onto cultural residues. Two lineal meters micropots were used. They received the fertilizer labeled with 15 N. Two treatments were established using labeled ammonium (NH4+-15 N) or nitrate (NO3-15 N). Two months after fertilization, four samples of the aerial part (two lineal meters) for treatment in the portions that did not receive the fertilizer-15 N, were taken in order to evaluated the fitomass production (Mg ha-1) and N-total accumulated (kg ha-1). This evaluation was repeated every two months up to complete five of them. Two leaves (leaves with 3 deg C visible auricle) were collected from plants that were in a middle of the micropots (15 N) and in corresponding positions in the adjacent rows, to evaluated the concentration of 15 N. There was a larger absorption of the nitrate-N (30.5%) than of the ammonium-N (21.2%). On the other hand, in the soil the results showed larger ammonium-15 N residual effect concentration, probably due to microorganism immobilization. (author)

  20. Understanding the impact of the central atom on the ionic liquid behavior: phosphonium vs ammonium cations.

    Science.gov (United States)

    Carvalho, Pedro J; Ventura, Sónia P M; Batista, Marta L S; Schröder, Bernd; Gonçalves, Fernando; Esperança, José; Mutelet, Fabrice; Coutinho, João A P

    2014-02-14

    The influence of the cation's central atom in the behavior of pairs of ammonium- and phosphonium-based ionic liquids was investigated through the measurement of densities, viscosities, melting temperatures, activity coefficients at infinite dilution, refractive indices, and toxicity against Vibrio fischeri. All the properties investigated are affected by the cation's central atom nature, with ammonium-based ionic liquids presenting higher densities, viscosities, melting temperatures, and enthalpies. Activity coefficients at infinite dilution show the ammonium-based ionic liquids to present slightly higher infinite dilution activity coefficients for non-polar solvents, becoming slightly lower for polar solvents, suggesting that the ammonium-based ionic liquids present somewhat higher polarities. In good agreement these compounds present lower toxicities than the phosphonium congeners. To explain this behavior quantum chemical gas phase DFT calculations were performed on isolated ion pairs at the BP-TZVP level of theory. Electronic density results were used to derive electrostatic potentials of the identified minimum conformers. Electrostatic potential-derived CHelpG and Natural Population Analysis charges show the P atom of the tetraalkylphosphonium-based ionic liquids cation to be more positively charged than the N atom in the tetraalkylammonium-based analogous IL cation, and a noticeable charge delocalization occurring in the tetraalkylammonium cation, when compared with the respective phosphonium congener. It is argued that this charge delocalization is responsible for the enhanced polarity observed on the ammonium based ionic liquids explaining the changes in the thermophysical properties observed. PMID:24527930

  1. Understanding the impact of the central atom on the ionic liquid behavior: Phosphonium vs ammonium cations

    Energy Technology Data Exchange (ETDEWEB)

    Carvalho, Pedro J.; Ventura, Sónia P. M.; Batista, Marta L. S.; Schröder, Bernd; Coutinho, João A. P., E-mail: jcoutinho@ua.pt [CICECO, Departamento de Química, Universidade de Aveiro, 3810-193 Aveiro (Portugal); Gonçalves, Fernando [Departamento de Biologia e CESAM (Centro de Estudos do Ambiente e do Mar), Universidade de Aveiro, 3810-193 Aveiro (Portugal); Esperança, José [Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, 2780-901 Oeiras (Portugal); Mutelet, Fabrice [Laboratoire Réactions et Génie des Procédés, CNRS (UPR3349), Nancy-Université, 1 rue Grandville, BP 20451 54001 Nancy (France)

    2014-02-14

    The influence of the cation's central atom in the behavior of pairs of ammonium- and phosphonium-based ionic liquids was investigated through the measurement of densities, viscosities, melting temperatures, activity coefficients at infinite dilution, refractive indices, and toxicity against Vibrio fischeri. All the properties investigated are affected by the cation's central atom nature, with ammonium-based ionic liquids presenting higher densities, viscosities, melting temperatures, and enthalpies. Activity coefficients at infinite dilution show the ammonium-based ionic liquids to present slightly higher infinite dilution activity coefficients for non-polar solvents, becoming slightly lower for polar solvents, suggesting that the ammonium-based ionic liquids present somewhat higher polarities. In good agreement these compounds present lower toxicities than the phosphonium congeners. To explain this behavior quantum chemical gas phase DFT calculations were performed on isolated ion pairs at the BP-TZVP level of theory. Electronic density results were used to derive electrostatic potentials of the identified minimum conformers. Electrostatic potential-derived CHelpG and Natural Population Analysis charges show the P atom of the tetraalkylphosphonium-based ionic liquids cation to be more positively charged than the N atom in the tetraalkylammonium-based analogous IL cation, and a noticeable charge delocalization occurring in the tetraalkylammonium cation, when compared with the respective phosphonium congener. It is argued that this charge delocalization is responsible for the enhanced polarity observed on the ammonium based ionic liquids explaining the changes in the thermophysical properties observed.

  2. Enhanced Ionization of Phosphopeptide Using Ammonium Phosphate as Matrix Additive by MALDI-MS

    Institute of Scientific and Technical Information of China (English)

    ZHANG,Ying; LU,Hao-Jie; YANG,Peng-Yuan

    2008-01-01

    A new method based upon adding ammonium phosphate as a matrix additive to enhance the ionization efficiency of phosphopeptide in matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) was described. Furthermore, influences of different phosphate salts at various concentrations on the ionization efficiency of phosphopeptide were investigated systematically, finding that the signal intensity for phosphopeptide 48FQ[pS]EEQQQTEDELQDK63 digested from β-casein were 5 to 8 times increased in an optimized condition with 10 mmol/L ammonium monobasic phosphate or 3 to 4 times increased with 10 mmol/L ammonium dibasic phosphate as additive to matrix 2,5-dihydroxybenzoic acid, respectively. Compared with the most optimized matrix system that was currently reported for special ionization of phosphopeptides, the signal intensity of this phosphopeptide was also enhanced by twice when introducing 5 mmol/L ammonium dibasic phosphate into matrix 2,4,6-trihydroxyacetophenone. In addition, the mechanism was also discussed, assuming that the cooperation function of ammonium cation and phosphate anion was of great importance in enhancing the ionization efficiency of phosphopeptide in MALDI-MS.

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

    Institute of Scientific and Technical Information of China (English)

    Shuhua Xue; Katsumi Uchiyama; Hai-fang Li

    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 μg/mL showed a good linear relationship with R2 =0.9985,and the detection limit was(S/N =3)3.6 × 10-4 μg/mL.The relative standard deviation was 2.8%(n =11)by calculating at 0.18 μg/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.

  4. Preparation of anhydrous magnesium chloride in a gas-solid reaction with ammonium carnallite

    Institute of Scientific and Technical Information of China (English)

    Zhou Ningbo; Chen Baizhen; He Xinkuai; Li Yibing

    2006-01-01

    Dehydrated ammonium carnallite was synthesized with bischofite from salt lake and ammonium chloride solution in a 1:1 molar ratio of MgCl2:NH4Cl,dehydrated at 160℃ for about 4 h.The yield was above 85%.The product was then mixed with solid-state ammonium chloride with a 1:4 mass ratio for the further dehydration at 410℃.The decomposition of NH4Cl made a pressure of NH3 at 30.5 kPa to prevent the hydrolysis of ammonium carnallite.The anhydration of magnesium chloride was achieved at 700℃.The results showed that anhydrous magnesium chloride contains magnesium oxide in an amount that was less than 0.1% by weight.XRD pattern and SEM micrograph showed a good dispersion of ammonium carnallite and anhydrous magnesium chloride crystals with well-distributed big grains,just enough to meet the need for the production of magnesium metal in the electrolysis process.

  5. Isolation and identification of bacteria responsible for simultaneous anaerobic ammonium and sulfate removal

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Sulfate-dependent anaerobic ammonium oxidation is a novel biological reaction,in which ammonium is oxidized with sulfate as the electron acceptor under anoxic conditions.Ammonium and sulfate are cosmopolitan chemical species which are an integral part of the global nitrogen and sulfur cycles.A detailed exploration of sulfate-dependent anaerobic ammonium oxidation is quite practical.In this work,a bacterial strain named ASR has been isolated from an anaerobic ammonia and sulfate removing reactor working under steady-state.On the basis of electron microscopy,physiological tests and 16S rDNA phylogenetic sequence analysis,the strain ASR is found to be related to Bacillus benzoevorans.According to the biological carbon source utilization test,the strain ASR could use many carbon sources.Its optimum pH value and temperature were 8.5 and 30 °C,respectively.The test proves that the strain ASR is able to use sulfate to oxidize ammonia anaerobically.The maximum ammonia and sulfate removal rates were 44.4% and 40.0%,respectively.The present study provided biological evidence for the confirmation and development of sulfate-dependent anaerobic ammonium oxidation and brought new insights into the global nitrogen and sulfur cycles.

  6. Characteristics of simultaneous ammonium and phosphate adsorption from hydrolysis urine onto natural loess.

    Science.gov (United States)

    Jiang, Shanqing; Wang, Xiaochang; Yang, Shengjiong; Shi, Honglei

    2016-02-01

    Nutrient recovery from human urine is a promising pretreatment of domestic wastewater and provides a sustainable recyclability of N and P. In this study, batch experiments were conducted to identify the characteristics of natural loess (NL) for the adsorption and recovery of ammonium and phosphate from hydrolysis urine (HU). The adsorption mechanisms, the adsorption kinetics and isotherms, as well as the major influencing factors, such as pH and temperature, were investigated. Results revealed that adsorption of ammonium occurred by means of ion exchange and molecule adsorption with the ≡ Si-OH groups, while phosphate adsorption was based on the calcium phosphate precipitation reaction and formation of inner-sphere complexes with ≡ M-OH groups. The adsorption processes of ammonium and phosphate were well described by the pseudo-second-order kinetic model and the Freundlich isotherm model. Adsorption of phosphate was endothermic, while ammonium adsorption was exothermic. Furthermore, the maximum ammonium and phosphate adsorption capacities of NL was 23.24 mg N g(-1) and 4.01 mg P g(-1) at an initial pH of 9 and 10, respectively. Results demonstrated that nutrient-adsorbed NL used as compound fertilizer or conventional fertilizer superaddition was feasible for its high contents of N and P as well as its environmental friendliness.

  7. Evaluation of natural zeolite clinoptilolite efficiency for the removal of ammonium and nitrate from aquatic solutions

    Directory of Open Access Journals (Sweden)

    Mozhdeh Murkani

    2015-01-01

    Full Text Available Background: Surface water and groundwater pollution with various forms of nitrogen such as ammonium and nitrate ions is one of the main environmental risks. The major objectives of this study were to evaluate the capacity of natural zeolite (clinoptilolite to remove NO3– and NH4+ from polluted water under both batch and column conditions. Methods: The laboratory batch and column experiments were conducted to investigate the feasibility of clinoptilolite as the adsorbent for removal of nitrate (NO3– and ammonium (NH4+ ions from aqueous solution. The effects of pH, clinoptilolite dosage, contact time, and initial metal ion concentration on NO3– and NH4+ removal were investigated in a batch system. Results: Equilibrium time for NO3– and NH4+ ions exchange was 60 minutes and the optimum adsorbent dosage for their removal was 1 and 2.5 g/L, respectively. The adsorption isotherm of reaction (r> 0.9 and optimum entered concentration of ammonium and nitrate (30 and 6.5 mg/L, respectively were in accordance with Freundlich isotherm model. The ammonium removal rate increased by 98% after increasing the contact time. Conclusion: Our findings confirmed that natural Clinoptilolite can be used as one of effective, suitable, and low-costing adsorbent for removing ammonium from polluted waters.

  8. Accurate Measurement of the in vivo Ammonium Concentration in Saccharomyces cerevisiae

    Directory of Open Access Journals (Sweden)

    Hugo F. Cueto-Rojas

    2016-04-01

    Full Text Available Ammonium (NH4+ is the most common N-source for yeast fermentations, and N-limitation is frequently applied to reduce growth and increase product yields. While there is significant molecular knowledge on NH4+ transport and assimilation, there have been few attempts to measure the in vivo concentration of this metabolite. In this article, we present a sensitive and accurate analytical method to quantify the in vivo intracellular ammonium concentration in Saccharomyces cerevisiae based on standard rapid sampling and metabolomics techniques. The method validation experiments required the development of a proper sample processing protocol to minimize ammonium production/consumption during biomass extraction by assessing the impact of amino acid degradation—an element that is often overlooked. The resulting cold chloroform metabolite extraction method, together with quantification using ultra high performance liquid chromatography-isotope dilution mass spectrometry (UHPLC-IDMS, was not only more sensitive than most of the existing methods but also more accurate than methods that use electrodes, enzymatic reactions, or boiling water or boiling ethanol biomass extraction because it minimized ammonium consumption/production during sampling processing and interference from other metabolites in the quantification of intracellular ammonium. Finally, our validation experiments showed that other metabolites such as pyruvate or 2-oxoglutarate (αKG need to be extracted with cold chloroform to avoid measurements being biased by the degradation of other metabolites (e.g., amino acids.

  9. Excretion of ammonium by a nifL mutant of Azotobacter vinelandii fixing nitrogen.

    Science.gov (United States)

    Bali, A; Blanco, G; Hill, S; Kennedy, C

    1992-05-01

    A mutation in the gene upstream of nifA in Azotobacter vinelandii was introduced into the chromosome to replace the corresponding wild-type region. The resulting mutant, MV376, produced nitrogenase constitutively in the presence of 15 mM ammonium. When introduced into a nifH-lacZ fusion strain, the mutation permitted beta-galactosidase production in the presence of ammonium. The gene upstream of nifA is therefore designated nifL because of its similarity to the Klebsiella pneumoniae nifL gene in proximity to nifA, in mutant phenotype, and in amino acid sequence of the gene product. The A. vinelandii nifL mutant MV376 excreted significant quantities of ammonium (approximately 10 mM) during diazotrophic growth. In contrast, ammonium excretion during diazotrophy was much lower in a K. pneumoniae nifL deletion mutant (maximum, 0.15 mM) but significantly higher than in NifL+ K. pneumoniae. The expression of the A. vinelandii nifA gene, unlike that of K. pneumoniae, was not repressed by ammonium. PMID:1622243

  10. An Electronic Tongue Designed to Detect Ammonium Nitrate in Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Inmaculada Campos

    2013-10-01

    Full Text Available An electronic tongue has been developed to monitor the presence of ammonium nitrate in water. It is based on pulse voltammetry and consists of an array of eight working electrodes (Au; Pt; Rh; Ir; Cu; Co; Ag and Ni encapsulated in a stainless steel cylinder. In a first step the electrochemical response of the different electrodes was studied in the presence of ammonium nitrate in water in order to further design the wave form used in the voltammetric tongue. The response of the electronic tongue was then tested in the presence of a set of 15 common inorganic salts; i.e.; NH4NO3; MgSO4; NH4Cl; NaCl; Na2CO3; (NH42SO4; MgCl2; Na3PO4; K2SO4; K2CO3; CaCl2; NaH2PO4; KCl; NaNO3; K2HPO4. A PCA plot showed a fairly good discrimination between ammonium nitrate and the remaining salts studied. In addition Fuzzy Art map analyses determined that the best classification was obtained using the Pt; Co; Cu and Ni electrodes. Moreover; PLS regression allowed the creation of a model to correlate the voltammetric response of the electrodes with concentrations of ammonium nitrate in the presence of potential interferents such as ammonium chloride and sodium nitrate.

  11. The mechanism for production of beryllium fluoride from the product of ammonium fluoride processing of beryllium- containing raw material

    Science.gov (United States)

    Kraydenko, R. I.; Dyachenko, A. N.; Malyutin, L. N.; Petlin, I. V.

    2016-06-01

    The technique of fluorite-phenacite-bertrandite ores from Russian Ermakovskoe deposit processing by ammonium bifluoride is described. To determine the temperature mode and the thermal dissociation mechanism of ammonium tetrafluoroberyllate (the product of ammonium-fluoride leaching of the ore) the TG/DTA have been carried out. By IR spectroscopy and XRD the semi-products of ammonium tetrafluoroberyllate thermal dissociation have been identified. The hygroscopic low-temperature beryllium fluoride forms higher than 380°C. The less hydroscopic form of BeF2 have been produced at 600°C.

  12. Pathway of ammonium assimilation in a marine diatom determined with the radiotracer 13N

    International Nuclear Information System (INIS)

    In unicellular algae, ammonium can be assimilated into glutamate through the action of glutamate dehydrogenase (GDH) or into glutamine through the sequential activities of glutamine synthetase and glutamate 2-oxoglutarate amidotransferase (GS-GOGAT pathway). We have shown that the first radio-labeled product of assimilation of 13NH4+ (t1/2 = 10 min) was glutamine in the marine diatom Thalassiosira pseudonana (Hustedt). When GS-GOGAT was inhibited with methionine sulfoximine, the incorporation of radioactivity into both glutamine and glutamate was blocked, implying that the radiolabeled glutamate is formed from glutamine. Glutamine was also the first labeled product when the intracellular concentration of ammonium was elevated by preincubation with unlabeled ammonium. The results indicate that the GS-GOGAT pathway is the primary pathway for the assimilation of nitrogen in T. pseudonana

  13. Preliminary Study On The Precipitation Of Ammonium Carbonate (AUC) From Uranylfluoride (UO2F2) Solution

    International Nuclear Information System (INIS)

    The preliminary studies on the precipitation process of ammonium uranyl carbonate (AUC)-(NH4)4UO2(CO3)3 from the UO2F2-HF solution system by using precipitation agent of ammonium carbonate (AC)-(NH4)2CO3 and on preparation ability of UO2 powder via AUC route are shown in this report. Our analysis results suggested that a product, identified as ammonium uranyl fluoride (AUF), was found along with the AUC precipitate. In order to prevent the formation of the undesirable AUF precipitate, the AUC precipitation process was carried out in the stable pH media ∼ 9, uranium concentration of 100 g/L and molar ratio of C to U ≥ 7.5. (author)

  14. EVALUATION OF THE ANTIMICROBIAL EFFECTS OF NEW HETEROCYCLIC BIS-QUATERNARY AMMONIUM COMPOUNDS ON BIOFILMS

    Directory of Open Access Journals (Sweden)

    OANA E. CONSTANTIN

    2016-07-01

    Full Text Available Considering the well-known mechanism of adaptable resistance of microorganisms to chemical compounds through biofilms formation and the widespread use of N-heterocyclic quaternary ammonium salts (QAC as disinfectants, in this study we have evaluate the effect of 8 newly synthesized symmetrical and unsymmetrical diquaternary ammonium salts of 1,2-bis-(4-pyridil-ethane on bacterial biofilms produced by three different bacterial strains. The effect of the exposure to quaternary ammonium salts on biofilm communities was investigated within biofilms obtained in a conventional testing system, on stainless steel and glass surfaces. Differential plate counts were used to characterize the developed communities and the effects of QAC exposure and the results were correlated with epifluorescence microphotographs. The data obtained revealed a significant reduction of bacterial cells in the biofilms tested with 4-7 log CFU for all the QAC.

  15. Synthesis of nano-crystalline hydroxyapatite and ammonium sulfate from phosphogypsum waste

    Energy Technology Data Exchange (ETDEWEB)

    Mousa, Sahar, E-mail: dollyriri@yahoo.com [Inorganic Chemistry Department, National Research Centre, Dokki, P.O.Box:12622, Postal code: 11787 Cairo (Egypt); King Abdulaziz University, Science and Art College, Chemistry Department, Rabigh Campus, P.O. Box:344, Postal code: 21911 Rabigh (Saudi Arabia); Hanna, Adly [Inorganic Chemistry Department, National Research Centre, Dokki, P.O.Box:12622, Postal code: 11787 Cairo (Egypt)

    2013-02-15

    Graphical abstract: TEM micrograph of dried HAP at 800 °C. -- Abstract: Phosphogypsum (PG) waste which is derived from phosphoric acid manufacture by using wet method was converted into hydroxyapatite (HAP) and ammonium sulfate. Very simple method was applied by reacting PG with phosphoric acid in alkaline medium with adjusting pH using ammonia solution. The obtained nano-HAP was dried at 80 °C and calcined at 600 °C and 900 °C for 2 h. Both of HAP and ammonium sulfate were characterized by X-ray diffraction (XRD) and infrared spectroscopy (IR) to study the structural evolution. The thermal behavior of nano-HAP was studied; the particle size and morphology were estimated by using transmission electron microscopy (TEM) and scanning electron microscopy (SEM). All the results showed that HAP nano-crystalline and ammonium sulfate can successfully be produced from phosphogypsum waste.

  16. Effect of ammonium on nitrous oxide emission during denitrification with different electron donors

    Institute of Scientific and Technical Information of China (English)

    Guangxue Wu; Xiaofeng Zhai; Chengai Jiang; Yuntao Guan

    2013-01-01

    Nitrous oxide (N2O) emission during denitrification is receiving intensive attention due to its high potential to cause greenhouse effects.In this study,denitrifiers were acclimated in sequencing batch reactors with methanol or acetate as the electron donor and nitrate as the electron acceptor.The effects of ammonium on N2O emission were examined in batch experiments with various electron donors.With the addition of ammonium,N2O emission increased under all the examined conditions compared to experiments without ammonium addition.With different electron donors,the highest ratio of N2O emission to the removed oxidized nitrogen was 0.70% for methanol,5.34% for acetate,and 34.79% for polyhydroxybutyrate.

  17. Experimental Research on Removing Suspended Solids and Ammonium Ions from Sludge Liquor

    Directory of Open Access Journals (Sweden)

    Kasparas Gražinskas

    2014-10-01

    Full Text Available The article investigates the processes of removing suspended solids and ammonium ions from sludge liquor. Experimental research was carried out at the Water Management Department laboratory of Vilnius Gediminas Technical University applying an experimental bench made of filters equipped with the zeolites of a different fraction and other appliances. Laboratory testing looked at the use of natural sorbent zeolite for removing ammonium ions from sludge liquor mixing liquid with powdered zeolite and filtering through zeolite filter media. Research was carried out employing the particles of zeolite 1.0–1.5 mm; 2.0–2.5 mm; 2.5–3.15 mm in diameter. The highest efficiency of removing ammonium ions reached 76% and was obtained using zeolite particles 2.0–2.5 mm in diameter.

  18. Preparation of uranium dioxide by thermal decomposition and direct reduction of ammonium uranate

    International Nuclear Information System (INIS)

    The thermal decomposition of ammonium uranate has been studied by infrared spectroscopy, and X-ray diffraction. It has been show that ammonia remains in the solid until substantially 350 Centigrade degrees, when gaseous nitrogen is released. It is concluded that compounds derived from the calcination of ammonium uranate at atmospheric pressure, produced amorphous U O3 at about 350-400 Centigrade degrees and transform to U3 O8 via α - U O3 and/or α - U O3. The object of this study was to obtain reliable fundamental information regarding the character of the pure carbon monoxide-ammonium uranate-uranium trioxide-uranium octaoxide reaction, in the range of temperatures that has been used in commercial reduction processes. Through the use of high-purity samples and by the proper control of incidental variable, this object was realized. (Author)

  19. Expression, purification and crystallization of the ammonium transporter Amt-1 from Archaeoglobus fulgidus

    Energy Technology Data Exchange (ETDEWEB)

    Andrade, Susana L. A., E-mail: sandrad@uni-goettingen.de; Dickmanns, Antje; Ficner, Ralf; Einsle, Oliver, E-mail: sandrad@uni-goettingen.de [Abteilung Molekulare Strukturbiologie, Institut für Mikrobiologie und Genetik, Georg-August-Universität Göttingen, Justus-von-Liebig-Weg 11, 37077 Göttingen (Germany)

    2005-09-01

    The ammonium transporter Amt-1 from the cytoplasmic membrane of the hyperthermophilic archaeon A. fulgidus has been purified and crystallized. Ammonium transporters (Amts) are a class of membrane-integral transport proteins found in organisms from all kingdoms of life. Their key function is the transport of nitrogen in its reduced bioavailable form, ammonia, across cellular membranes, a crucial step in nitrogen assimilation for biosynthetic purposes. The genome of the hyperthermophilic archaeon Archaeoglobus fulgidus has been annotated with three individual genes for ammonium transporters, amt1–3, the roles of which are as yet unknown. The amt1 gene product has been produced by heterologous overexpression in Escherichia coli and the resulting protein has been purified to electrophoretic homogeneity. Crystals of Amt-1 have been obtained by sitting-drop vapour diffusion and diffraction data have been collected.

  20. Impact of flow conditions on ammonium uptake and microbial community structure in benthic biofilms

    Science.gov (United States)

    Arnon, Shai; Yanuka, Keren; Nejidat, Ali

    2010-05-01

    Excess nitrogen in surface waters is widely recognized to be a major global problem that adversely affects ecosystems, human health, and the economy. Today, most efforts to understand and model nutrient dynamics at large scales relies on macro-scale parameterization, such as mean channel geometry and velocity with uniform flow assumptions, as well as gross averages of in-situ nutrient transformation rates. However, there is increasing evidence that nutrient transformations in hyporheic zone are regulated by coupling between physical, chemical, and microbiological processes. Ignoring this greatly hinders the estimation of average biochemical transformation rates under the variable flow conditions found in aquatic systems. We used a combination of macro- and micro-scale observations in laboratory flumes to show that interplay between hydrodynamic transport, redox gradients, and microbial metabolism controls ammonium utilization by hyporheic microbial communities. Biofilm structural characteristics were quantified using denaturing gradient gel electrophoresis (DGGE) and real time PCR, while redox and pH gradients were measured using microelectrodes. We found that overlying velocities had profound effect on ammonium uptake due to mass transfer of ammonium from the bulk water to the benthic biofilms, but also due to the delivery of oxygen into the sediment bed. Under laminar flow conditions we didn't observe any change of ammonium uptake as a response to increase in overlying velocity. However, under non-laminar conditions we observe monotonic increase in ammonium uptake, with the greatest uptake under the fastest flow condition. We will discuss ammonium uptake rates results in the context of the different microbial communities and the micro-scale observations that were obtained using the microelectrodes. We anticipate that combined knowledge of the response of the microbial community and bulk nitrogen utilization rates to flow conditions will support the development of

  1. Oxidation behavior of ammonium in a 3-dimensional biofilm-electrode reactor.

    Science.gov (United States)

    Tang, Jinjing; Guo, Jinsong; Fang, Fang; Chen, Youpeng; Lei, Lijing; Yang, Lin

    2013-12-01

    Excess nitrogenous compounds are detrimental to natural water systems and to human health. To completely realize autohydrogenotrophic nitrogen removal, a novel 3-dimensional biofilm-electrode reactor was designed. Titanium was electroplated with ruthenium and used as the anode. Activated carbon fiber felt was used as the cathode. The reactor was separated into two chambers by a permeable membrane. The cathode chamber was filled with granular graphite and glass beads. The cathode and cathode chamber were inhabited with domesticated biofilm. In the absence of organic substances, a nitrogen removal efficiency of up to 91% was achieved at DO levels of 3.42 +/- 0.37 mg/L when the applied current density was only 0.02 mA/cm2. The oxidation of ammonium in biofilm-electrode reactors was also investigated. It was found that ammonium could be oxidized not only on the anode but also on particle electrodes in the cathode chamber of the biofilm-electrode reactor. Oxidation rates of ammonium and nitrogen removal efficiency were found to be affected by the electric current loading on the biofilm-electrode reactor. The kinetic model of ammonium at different electric currents was analyzed by a first-order reaction kinetics equation. The regression analysis implied that when the current density was less than 0.02 mA/cm2, ammonium removal was positively correlated to the current density. However, when the current density was more than 0.02 mA/cm2, the electric current became a limiting factor for the oxidation rate of ammonium and nitrogen removal efficiency. PMID:24649670

  2. Degradation and bound-residue formation of nonylphenol in red soil and the effects of ammonium

    International Nuclear Information System (INIS)

    Fate of nonylphenol (NP) in soils and the effects of nitrogen fertilizers are unclear. Using 14C-tracer, we studied the aerobic and anaerobic degradation of 4-NP111 in a paddy red soil amended without and with ammonium chloride. Under oxic conditions, 4-NP111 had a half-life of 16.1 ± 1.6 days and minor mineralization (3.84 ± 0.02%), forming no extractable metabolite but abundant bound residues (60.9 ± 1.7%, mostly bound to humin) after 49 days of incubation. The ammonium amendment (8 mmol/kg soil) significantly inhibited the degradation (half-life of 68.0 ± 7.7 days), mineralization (2.0 ± 1.1%), and bound-residue formation (23.7 ± 0.2%). Under anoxic conditions, 4-NP111 did not degrade during 49 days of incubation and the ammonium amendment (40 mmol/kg soil) did not affect its persistence. Our results demonstrate that bound-residue formation was a major mechanism for NP dissipation in the red soil under oxic conditions and that chemical nitrogen fertilizer at average field application rate may already considerably increase NP recalcitrance in agricultural soils. -- Highlights:: • Aerobic mineralization of the nonylphenol isomer 4-NP111 in paddy red soil is minor. • Bound-residue formation is the major mechanism for aerobic NP degradation in soil. • The majority of the bound residues of NP are localized in soil humin fraction. • Amendment of soil by ammonium strongly increase the persistence of NP in oxic soil. • Amendment of soil by ammonium does not affect the recalcitrance of NP in anoxic soil. -- Formation of bound residues was the major mechanism in paddy red soil under oxic conditions for nonylphenol dissipation, which was significantly inhibited by amendment with ammonium

  3. An 15N study of the effects of nitrate, ammonium, and nitrate + ammonium nutrition on nitrogen assimilation in Zea mays L

    International Nuclear Information System (INIS)

    A brief review of the literature on the effects of nitrate and ammonium nitrogen sources on plant growth, and the assimilation of those nitrogen sources, has been presented. It was concluded that ammonium nutrition produces optimum growth, with nitrate + ammonium being a better nitrogen source than only nitrate. Leaf blade nitrate reductase activity exceeded that of the root in nitrate-fed plants, suggesting that the shoot is the major region of nitrate assimilation. This is further supported by the results of xylem exudate analysis, where 93% of the newly-absorbed nitrogen exported by the roots was detected as nitrate. Evidence in support of this hypothesis was also obtained by studying the distribution of 15N in the various nitrogenous compounds. The effects of nitrogen source on plant growth, organic nitrogen and inorganic nitrogen contents, and the rates of incorporation into nitrogenous compounds were studied. The observed differences were explained with reference to the effects of the various nitrogen sources on the physiology of the plants. The experimental techniques included assays of the enzymes nitrate reductase and glutamine synthetase, whole plant growth studies, and the analysis of nitrogenous compounds of xylem exudate and those extracted from the leaf blade, leaf base, and root regions of maize plants after feeding with a nutrient solution containing nitrogen as 15N

  4. Formation of ammonium sulphate in water droplets exposed to gaseous sulphur dioxide and ammonia

    Energy Technology Data Exchange (ETDEWEB)

    van den Heuvel, A.P.; Mason, B.J.

    1963-01-01

    The rate of formation of ammonium sulphate in water drops exposed to air containing known concentrations of gaseous sulphur dioxide and ammonia has been measured. The mass of sulphate formed is proportional to the product of the surface area of the drops and the time of exposure. Extrapolation of the laboratory results to the atmosphere suggests that the large condensation nuclei 0.2 micronammonium sulphate, are formed by the absorption of SO/sub 2/ and NH/sub 3/ in cloud and fog droplets.

  5. The performance of ammonium exchanged zeolite for the biodegradation of petroleum hydrocarbons migrating in soil water.

    Science.gov (United States)

    Freidman, Benjamin L; Gras, Sally L; Snape, Ian; Stevens, Geoff W; Mumford, Kathryn A

    2016-08-01

    Nitrogen deficiency has been identified as the main inhibiting factor for biodegradation of petroleum hydrocarbons in low nutrient environments. This study examines the performance of ammonium exchanged zeolite to enhance biodegradation of petroleum hydrocarbons migrating in soil water within laboratory scale flow cells. Biofilm formation and biodegradation were accelerated by the exchange of cations in soil water with ammonium in the pores of the exchanged zeolite when compared with natural zeolite flow cells. These results have implications for sequenced permeable reactive barrier design and the longevity of media performance within such barriers at petroleum hydrocarbon contaminated sites deficient in essential soil nutrients. PMID:27132074

  6. Short-term temporal variability of ammonium and urea uptake by Alexandrium catenella (Dinophyta) in cultures

    OpenAIRE

    Jauzein, Cecile; Collos, Yves; Garces, E.; Vila, M.; Maso, M

    2008-01-01

    In batch cultures of four Mediterranean strains (from France, Italy, and Spain) of Alexandrium catenella (Whedon et Kof.) Balech growing on a daily light cycle, ammonium and urea uptake were estimated by the N-15 tracer technique. Ammonium uptake could be described by Michaelis-Menten kinetics along a substrate gradient of 0.1-10 mu gat N.L-1 for the four strains, while two different patterns were observed for urea uptake with Michaelis-Menten kinetics for one strain and linear kinetics for t...

  7. Modeling conversion of ammonium diuranate (ADU) into uranium dioxide (UO2) powder

    Science.gov (United States)

    Hung, Nguyen Trong; Thuan, Le Ba; Khoai, Do Van; Lee, Jin-Young; Jyothi, Rajesh Kumar

    2016-10-01

    In the paper, Brandon mathematical model that describes the relationship between the essential fabrication parameters [reduction temperature (TR), calcination temperature (TC), calcination time (tC) and reduction time (tR)] and specific surface area of ammonium diuranate (ADU)-derived UO2 powder products was established. The proposed models can be used to predict and control the specific surface area of UO2 powders prepared through ADU route. Suitable temperatures for conversion of ADU and ammonium uranyl carbonate (AUC) was examined with the proposed model through assessment of the sinterability of UO2 powders.

  8. AMMONIUM TREATMENT OF NATURAL CLINOPTILOLITE AND ITS CHARACTER OF ION—EXCHANGE

    Institute of Scientific and Technical Information of China (English)

    LiuYifan; WangYuying

    1998-01-01

    Ammonium can change the type of natural clinoptilolite from Jinyun of Zhejiang Province of China.The character of exchange and selectivity of ammonium type clinoptilolite to the alkali and alkaline-earth metal were investigated,the heatresistance and nitric acid-resistance of natural clinoptilolite were discussed.All types of clinoptilolite were researched by means of X-ray,IR spectroscopy,DTA analyses.The ion exchange was experimented by column operation,indicating that the valid amount of exchange capacity of NH4+ type clinoptiloties is more than 25mg/g.

  9. Inactivation of ANAMMOX communities under concurrent operation of anaerobic ammonium oxidation (ANAMMOX) and denitrification

    DEFF Research Database (Denmark)

    Chamchoi, N.; Nitisoravut, S.; Schmidt, Jens Ejbye

    2008-01-01

    A concurrent operation of anaerobic ammonium oxidation (ANAMMOX) and denitrification was investigated in a well known UASB reactor seeding with both ANAMMOX and anaerobic granular sludges. ANAMMOX activity was confirmed by hydroxylamine test and the hybridization of biomass using the gene probes...... of Amx 820 and EUB 338 mixed. Denitrification was observed through the reductions of both COD and nitrate–nitrite concentrations under anaerobic/anoxic conditions. By providing a stoichiometric ratio of nitrite to ammonium nitrogen with addition nitrate nitrogen, a gradual reduction of ANAMMOX activity...

  10. Development of miniaturized potentiometric nitrate- and ammonium selective electrodes for applications in water monitoring

    Energy Technology Data Exchange (ETDEWEB)

    Schwarz, J.; Kaden, H. [Kurt-Schwabe-Institut fuer Mess- und Sensortechnik e.V., Meinsberg (Germany); Pausch, G. [Umwelt- und Ingenieurtechnik GmbH, Dresden (Germany)

    2000-06-01

    Mobile analysis with potentiometric sensors is well suited for field measurements. Ion-selective electrodes (ISE) based on polymeric membranes for in-situ determination of nitrate and ammonium contents in ground water, drinking water and surface water have been developed. The ISE are integrated in a multisensor module (MSM) for monitoring these ions over longer time intervals. The receptor is a PVC-membrane with tridodecylammonium nitrate (TDDA) for nitrate- and nonactine for ammonium-electrodes as ionophores. As plasticizer dibutylphthalate (DBT) was used. The main parameters for assessing the efficiency of these ISE are presented. (orig.)

  11. Excretion of ammonium by a nifL mutant of Azotobacter vinelandii fixing nitrogen.

    OpenAIRE

    Bali, A.; Blanco, G.; Hill, S.; Kennedy, C

    1992-01-01

    A mutation in the gene upstream of nifA in Azotobacter vinelandii was introduced into the chromosome to replace the corresponding wild-type region. The resulting mutant, MV376, produced nitrogenase constitutively in the presence of 15 mM ammonium. When introduced into a nifH-lacZ fusion strain, the mutation permitted beta-galactosidase production in the presence of ammonium. The gene upstream of nifA is therefore designated nifL because of its similarity to the Klebsiella pneumoniae nifL gene...

  12. Fixed Ammonium in Major Types of Paddy Soils in Hunan Province,China

    Institute of Scientific and Technical Information of China (English)

    ZHANG YANGZHU; LIAO JIPEI; SUN YUHUAN; FENG YUEHUA; HUANG YUNXIANG

    2003-01-01

    The contents, affecting factors, seasonal changes and availability of fixed ammonium in major types ofpaddy soils derived from different parent materials in Hunan Province, China, were studied using the Silva-Bremner method by laboratory and pot experiments. Results showed that the content of fixed ammoniumin the plough horizons ranged from 88.3 mg kg-1 to 388.1 mg kg-1, with 273.2 ± 77.7 mg kg-1 on average,accounting for 11.2% of total soil N on average. Content of fixed ammonium decreased in the order of newlylacustrine clayey paddy soil > alluvial sandy paddy soil > purple clayey paddy soil > newly alluvial sandypaddy soil > yellow clayey paddy soil > reddish-yellow clayey paddy soil > granitic sandy paddy soil. Therewere four distribution patterns of fixed ammonium in the profiles to 1-m depth, i.e., increase with the depth,decrease with increasing depth, no distinct change with the depth, and abrupt increase or decrease in somehorizon. Percentage of fixed ammonium in total N increased with the depth in most of the soils. Fixationof NH4+ by soil was higher at 30 ℃ than at 20 ℃ and 40 ℃, and continuous submergence benefited thefixation of NH4+ in newly alluvial sandy paddy soil, purple clayey paddy soil and alluvial sandy paddy soil,while alternating wetting and drying contributed to the fixation of NH4+ in yellow clayey paddy soil mostly.Fixed ammonium content in the test paddy soils was significantly correlated with < 0.01 mm clay content(P < 0.05), but not with < 0.001 mm clay content, total N, organic N and organic matter. Fixed ammoniumcontent varied with rice growth stages. Application of N fertilizer promoted fixation of NH4+ by soil, and Nuptake by rice plant promoted release of fixed ammonium from the soil. Recently fixed ammonium in paddysoil after N fertilizer application was nearly 100% available to rice plant, while native fixed ammonium wasonly partly available, varying with the soil type and rice type.

  13. Antioxidant Potential of Momordica Charantia in Ammonium Chloride-Induced Hyperammonemic Rats

    OpenAIRE

    A. Justin Thenmozhi; Subramanian, P.

    2011-01-01

    The present study was aimed to investigate the antioxidant potential of Momordica charantia fruit extract (MCE) in ammonium chloride-induced (AC) hyperammonemic rats. Experimental hyperammonemia was induced in adult male Wistar rats (180–200 g) by intraperitoneal injections of ammonium chloride (100 mg kg−1 body weight) thrice a week. The effect of oral administration (thrice a week for 8 consecutive weeks) of MCE (300 mg kg−1 body weight) on blood ammonia, plasma urea, serum liver marker enz...

  14. Modification of a Brazilian smectite clay with different quaternary ammonium salts

    Directory of Open Access Journals (Sweden)

    Maria Flávia Delbem

    2010-01-01

    Full Text Available In this work, a smectite clay from the State of Paraiba, Brazil, was treated with six different types of ammonium salts, which is an usual method to enhance the affinity between the clay and polymer for the preparation of nanocomposites. The clays, before and after modification, were characterized by X ray diffraction. The conformation of the salts within the platelets of the clay depended on the number of long alkyl chains of the salt. The thermal stability of the clays was also studied. The ammonium salts thermal decomposition was explained in light of their position within the organoclays.

  15. 40 CFR 721.6183 - Amides, from ammonium hydroxide - maleic anhydride polymer and hydrogenated tallow alkyl amines...

    Science.gov (United States)

    2010-07-01

    ... - maleic anhydride polymer and hydrogenated tallow alkyl amines, sodium salts, compds. with ethanolamine... Substances § 721.6183 Amides, from ammonium hydroxide - maleic anhydride polymer and hydrogenated tallow... subject to reporting. (1) The chemical substance identified as amides, from ammonium hydroxide -...

  16. Growth at low ammonium concentrations and starvation response as potential factors involved in niche differentiation among ammonia-oxidizing bacteria

    NARCIS (Netherlands)

    Bollmann, A.; Bär-Gilissen, M.J.; Laanbroek, H.J.

    2002-01-01

    In nature, ammonia-oxidizing bacteria have to compete with heterotrophic bacteria and plants for limiting amounts of ammonium. Previous laboratory experiments conducted with Nitrosomonas europaea suggested that ammonia-oxidizing bacteria are weak competitors for ammonium. To obtain a better insight

  17. The integration of methanogenesis with denitrification and anaerobic ammonium oxidation in an expanded granular sludge bed reactor

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The integration of methanogenesis with denitrification and anaerobic ammonium oxidation(ANAMMOX) was studied in an expanded granular sludge bed(EGSB) reactor in this work. Experimental results from the continuous treatment of wastewater with nitrite and ammonium, which lasted for 107 days, demonstrated that wastewater with high nitrite and ammonium could be anaerobically treated in an expanded granular sludge bed reactor. More than 91% to 97% of COD were removed at up to about 3.9 g COD/(L@d) of COD volumetric loading rate. More than 97% to 100% of nitrite was denitrified at up to about 0.8g NO2-N/(L@d), which is 16 times higher than that in a conventional activated sludge system with nitrification/denitrification(0.05g N/((L@d). No dissimilatory reduction of nitrite to ammonium occurred in the process. However, maximum of about 40% ammonium was found to be lost. Batch tests of 15 days with sludge from the reactor showed that 100% of nitrite was denitrified completely, and about 3% of ammonium was removed when only ammonium (34.3 mg/L) and nitrite(34.3 mg/L) were added into the sludge suspension medium. Furthermore, about 15% of ammonium amounts were lost with organic COD addition. It suggested that the methanogenesis in the system could enhance ANAMMOX because of intermediate hydrogen produced during methanogenesis.

  18. Aerobic physiology of redox-engineered Saccharomyces cerevisiae strains modified in the ammonium assimilation for increased NADPH availability

    DEFF Research Database (Denmark)

    Santos, Maria Margarida M. dos; Thygesen, G.; Kotter, P.;

    2003-01-01

    Recombinant strains altered in the ammonium assimilation pathways were constructed with the purpose of increasing NADPH availability. The NADPH-dependent glutamate dehydrogenase encoded by GDH1, which accounts for a major fraction of the NADPH consumption during growth on ammonium, was deleted, a...

  19. Oxidative desulfurization of diesel fuel using amphiphilic quaternary ammonium phosphomolybdate catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Qiu, Jianghua; Wang, Guanghui; Zeng, Danlin; Tang, Yan [College of Chemical Engineering and Technology, Wuhan University of Science and Technology, Wuhan 430081 (China); Wang, Meng; Li, Yanjun [College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072 (China)

    2009-12-15

    Phosphomolybdic acid (HPMo) modified respectively with tetramethyl ammonium chloride (TMAC), dodecyl trimethyl ammonium chloride (DTAC) and hexadecyl trimethyl ammonium chloride (HTAC) as the catalysts were prepared and characterized by FT-IR, XRD and SEM. The catalysts were evaluated for the oxidative desulfurization of benzothiophene (BT), dibenzothiophene (DBT) and straight-run diesel using hydrogen peroxide as an oxidant. Results show that all of the catalysts keep the Keggin structures and are finely dispersed with mixing of quaternary ammonium salts. Hexadecyl chains are more favorable to wrap up DBT to the catalytic center and form stable emulsion system with higher conversion rates of DBT. The shorter dodecyl chains can wrap up BT more suitably and bring smaller steric hindrance, which display higher conversion rates of BT. The oxidative reactions fit apparent first-order kinetics, and the apparent activation energies of DBT are much lower than those of BT. The desulfurization rate of straight-run diesel can be up to 84.4% with the recovery rate of 98.1% catalyzed by [HPMo][HTAC]{sub 2} in 2 h. When increasing the extraction times, the desulfurization rates increase, but the recovery rates of diesel decrease significantly. (author)

  20. Deciphering the molecular basis of ammonium uptake and transport in maritime pine.

    Science.gov (United States)

    Castro-Rodríguez, Vanessa; Assaf-Casals, Iman; Pérez-Tienda, Jacob; Fan, Xiaorong; Avila, Concepción; Miller, Anthony; Cánovas, Francisco M

    2016-08-01

    Ammonium is the predominant form of inorganic nitrogen in the soil of coniferous forests. Despite the ecological and economic importance of conifers, the molecular basis of ammonium uptake and transport in this group of gymnosperms is largely unknown. In this study, we describe the functional characterization of members of the AMT gene family in Pinus pinaster: PpAMT1.1, PpAMT1.2 and PpAMT1.3 (subfamily 1) and PpAMT2.1 and PpAMT2.3 (subfamily 2). Our phylogenetic analysis indicates that in conifers, all members of the AMT1 subfamily evolved from a common ancestor that is evolutionarily related to the ancient PpAMT1.2 gene. Individual AMT genes are developmentally and nutritionally regulated, and their transcripts are specifically distributed in different organs. PpAMT1.3 was predominantly expressed in the roots, particularly during N starvation and mycorrhizal interaction, whereas PpAMT2.3 was preferentially expressed in lateral roots. Immunolocalization studies of roots with varied nitrogen availability revealed that PpAMT1 and PpAMT2 proteins play complementary roles in the uptake of external ammonium. Heterologous expression in yeast and Xenopus oocytes revealed that the AMT genes encode functional transporters with different kinetics and with different capacities for ammonium transport. Our results provide new insights on how nitrogen is acquired and transported in conifers. PMID:26662862