Sample records for ammonium perchlorates

  1. Ammonium Perchlorate and Ammonium Perchlorate- Hydroxyl Terminated Polybutadiene Simulated Combustion

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    Rene Francisco Boschi Gonçalves


    Full Text Available The combustion simulation of ammonium perchlorate was carried out with the software Chemkin, in two steps: the burning behavior of pure ammonium perchlorate and the one of formulated ammonium perchlorate with hydroxyl terminated polybutadiene binder. In both cases, the room pressure varied in order to verify its influence in the system. The burning environment conditions were diverse. During the combustion process, the data obtained from the kinetic chemistry simulation software were compiled. The flame structure can be described by the molar fraction of the burning products and the temperature evolution from the surface of the material.

  2. Biodegradation of rocket propellant waste, ammonium perchlorate (United States)

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


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

  3. Perchlorate Exposure and Thyroid Function in Ammonium Perchlorate Workers in Yicheng, China

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    Hongxia Chen


    Full Text Available The impact of low level dust on the thyroid function of workers chronically exposed to ammonium perchlorate (AP is uncertain and controversial. The aim of this study was to examine whether workers in China with long-term (>3 years occupational exposure to low levels of AP dust had affected thyroid homeostasis. Mean occupational exposures to AP dust ranged from 0.43 to 1.17 mg/m3. Geometric means of post-shift urinary perchlorate levels were 20.5 µg/L for those exposed and 12.8 µg/L for the controls. No significant differences were found for thyroid function parameters of FT3, FT4, or log TSH or for TPO prevalence or thyroglobulin levels. Additionally, no differences in findings were observed for complete blood count (CBC, serum biochemical profile, or pulmonary function test. Median urinary iodine levels of 172 and 184 µg/L showed that the workers had sufficient iodine intake. This study found no effect on thyroid function from long term, low-level documented exposure to ammonium perchlorate. It is the first study to report both thyroid status parameters and urinary perchlorate, a biomarker of internal perchlorate exposure, in occupationally exposed workers in China.


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    Nahidh Kaseer


    Full Text Available 31Overall crystal growth kinetics for ammonium perchlorate in laboratory scale batch  agitated vessel crystallizer have been determined from batch experiments performed in an integral mode. The effects of temperature between 30-60ºC, seed size 0.07, 0.120 and 0.275 mm and stirrer speed 160, 340, and 480 rpm, on the kinetics of crystal growth were investigated. Two different methods, viz. polynomial fitting and initial derivative were used to predict the kinetics expression. In general both methods gave comparable results for growth kinetics estimation. The order of growth process is not more than two. The activation energy for crystal growth of ammonium perchlorate was determined and found  to be equal to 5.8 kJ/ mole.            Finally, the influence of the affecting parameters on the crystal growth rate gives general expression that had an obvious dependence of the growth rate on each variables of concern (temperature, seed size, and stirrer speed .The general overall growth rate expression had shown that super saturation is the most significant variable. While the positive dependence of the stirrer speed demonstrates the importance of the diffusional step in the growth rate model. Moreover, the positive dependence of the seed size demonstrate the importance of the surface integration  step in the growth rate model. All the studied variables tend to suggest that the growth rate characteristics  of ammonium perchlorate from aqueous solution commenced in a batch crystallizer are diffusion kinetic controlled process.

  5. Fabrication of ammonium perchlorate/copper-chromium oxides core-shell nanocomposites for catalytic thermal decomposition of ammonium perchlorate

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    Eslami, Abbas, E-mail: [Department of Inorganic Chemistry, Faculty of Chemistry, University of Mazandaran, P.O.Box 47416-95447, Babolsar (Iran, Islamic Republic of); Juibari, Nafise Modanlou [Department of Inorganic Chemistry, Faculty of Chemistry, University of Mazandaran, P.O.Box 47416-95447, Babolsar (Iran, Islamic Republic of); Hosseini, Seyed Ghorban [Department of Chemistry, Malek Ashtar University of Technology, P.O. Box 16765-3454, Tehran (Iran, Islamic Republic of)


    The ammonium perchlorate/Cu(II)-Cr(III)-oxides(AP/Cu-Cr-O) core-shell nanocomposites were in-situ prepared by deposition of copper and chromium oxides on suspended ammonium perchlorate particles in ethyl acetate as solvent. The results of differential scanning calorimetery (DSC) and thermal gravimetric analysis (TGA) experiments showed that the nanocomposites have excellent catalytic effect on the thermal decomposition of AP, so that the released heat increases up to about 3-fold over initial values, changing from 450 J/g for pure AP to 1510 J/g for most appropriate mixture. For better comparison, single metal oxide/AP core-shell nanocomposite have also been prepared and the results showed that they have less catalytic effect respect to mixed metal oxides system. Scanning electron microscopy (SEM) results revealed homogenous deposition of nanoparticles on the surface of AP and fabrication of core-shell structures. The kinetic parameters of thermal decomposition of both pure AP and AP/Cu-Cr-O samples have been calculated by Kissinger method and the results showed that the values of pre-exponential factor and activation energy are higher for AP/Cu-Cr-O nanocomposite. The better catalytic effect of Cu-Cr-O nanocomposites is probably attributed to the synergistic effect between Cu{sup 2+} and Cr{sup 3+} in the nanocomposites, smaller particle size and more crystal defect. - Highlights: • The Cu-Cr-O nanoparticles were synthesized by chemical liquid deposition method. • Then, the AP/Cu-Cr-O core-shell nanocomposites were prepared. • The core-shell samples showed high catalytic activity for AP decomposition. • Thermal decomposition of samples occurs at lower temperature range.

  6. High Pressure Burn Rate Measurements on an Ammonium Perchlorate Propellant

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    Glascoe, E A; Tan, N


    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

  7. Engineered Intrinsic Bioremediation of Ammonium Perchlorate in Groundwater (United States)


    drive an aquifer anaerobic by biostimulation. Project tasks are to: 1) isolate and characterize novel perchlorate-reducing bacteria in addition to...bioremediation with the GA application is to engineer natural subsurface microbial communities ( aquifer biofilms) to give them the ability to degrade (reduce...hydrogen as electron donor for chloroform cometabolism by a mixed, methanogenic culture. Environ. Sci. Technol. 31: 880–885 Weuster-Botz, D. and Wandrey

  8. In-Situ Bioreduction and Removal of Ammonium Perchlorate (United States)


    recently, it was demonstrated that solid fertilizers not derived from the Chilean deposits and commonly used for the hydroponic growth of various fruit...owing to the increasing use of hydroponic farming techniques for the production of a wide variety of plants for human consumption throughout the...such as tobacco and lettuce the perchlorate accumulates and persists during processing into the final shelf products, such as cigarettes, cigars and

  9. Experimental investigation on the heterogeneous kinetic process of the low thermal decomposition of ammonium perchlorate particles

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    Longuet, Baptiste [Laboratoire Energetique Explosions et Structures Universite d' Orleans (Germany); Gillard, Philippe [Laboratoire Energetic Explosions et Structures, Universite d' Orleans, Bourges (France)


    The thermal decomposition of ammonium perchlorate has been extensively studied in the past. Nevertheless, the various results published illustrate, on the one hand, significant differences regarding the influence of different parameters on the decomposition and on the other hand, a lack of useful quantitative laws to predict the thermal behaviour of this crystal under a range of conditions (temperature, duration of exposure, presence of confinement). (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  10. Tetranitroacetimidic acid: a high oxygen oxidizer and potential replacement for ammonium perchlorate. (United States)

    Vo, Thao T; Parrish, Damon A; Shreeve, Jean'ne M


    Considerable work has been focused on developing replacements for ammonium perchlorate (AP), a primary choice for solid rocket and missile propellants, due to environmental concerns resulting from the release of perchlorate into groundwater systems [corrected]. Additionally, the generation of hydrochloric acid contributes to high concentrations of acid rain and to ozone layer depletion. En route to synthesizing salts that contain cationic FOX-7, a novel, high oxygen-containing oxidizer, tetranitroacetimidic acid (TNAA), has been synthesized and fully characterized. The properties of TNAA were found to be exceptional, with a calculated specific impulse exceeding that of AP, leading to its high potential as a replacement for AP. TNAA can be synthesized easily in a one-step process by the nitration of FOX-7 in high yield (>93%). The synthesis, properties, and chemical reactivity of TNAA have been examined.

  11. Nano-Ammonium Perchlorate: Preparation, Characterization, and Evaluation in Composite Propellant Formulation (United States)

    Kumari, A.; Mehilal; Jain, S.; Jain, M. K.; Bhattacharya, B.


    Nanomaterials are finding applications in explosives and propellant formulations due to their large surface area and high surface energy. This high surface energy is responsible for the low activation energy and increase in burning rate of the composition. Therefore, a successful attempt has been made to prepare nano-ammonium perchlorate using a nonaqueous method by dissolving ammonium perchlorate (AP) in methanol followed by adding the dissolved AP to the hydroxyl-terminated polybutadiene (HTPB), homogenization, and vacuum distillation of the solvent. The nano-AP thus formed was characterized using a NANOPHOX particle size analyzer (Sympatec, Germany), transmission electron microscopy (FEI, Hillsboro, OR), X-ray diffraction (PANalytical B.V., The Netherlands) and scanning electron microscopy (Ikon Analytical Equipment Pvt. Ltd., Mumbai, India) for particle size, purity, and morphology, respectively. The thermal behavior of nano-AP was also studied using differential thermal analysis-thermo gravimetric analysis (DTA-TGA). The data indicated that the particle size of the prepared AP was in the range of 21-52 nm and the thermal decomposition temperature was lower than that of coarse AP. Characterized nano-AP was subsequently used in composite propellant formulation up to 5% with 86% solid loading and studied for different properties. The results showed a 14% increase in burning rate in comparison to standard propellant composition with desired mechanical properties.

  12. Change of iodine load and thyroid homeostasis induced by ammonium perchlorate in rats. (United States)

    Chen, Hong-Xia; Ding, Miao-Hong; Liu, Qin; Peng, Kai-Liang


    Ammonium perchlorate (AP), mainly used as solid propellants, was reported to interfere with homeostasis via competitive inhibition of iodide uptake. However, detailed mechanisms remain to be elucidated. In this study, AP was administered at 0, 130, 260 and 520 mg/kg every day to 24 male SD rats for 13 weeks. The concentrations of iodine in urine, serum thyroid hormones levels, total iodine, relative iodine and total protein, and malondialdehyde (MDA), superoxide dismutase (SOD) and catalase (CAT) activity in thyroid tissues were measured, respectively. Our results showed that high-dose perchlorate induced a significant increase in urinary iodine and serum thyroid stimulating hormone (TSH), with a decrease of total iodine and relative iodine content. Meanwhile, free thyroxine (FT4) was decreased and CAT activity was remarkably increased. Particularly, the CAT activity was increased in a dose-dependent manner. These results suggested that CAT might be enhanced to promote the synthesis of iodine, resulting in elevated urinary iodine level. Furthermore, these findings suggested that iodine in the urine and CAT activity in the thyroid might be used as biomarkers for exposure to AP, associated with thyroid hormone indicators such as TSH, FT4.

  13. Nitrated graphene oxide and its catalytic activity in thermal decomposition of ammonium perchlorate

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    Zhang, Wenwen; Luo, Qingping; Duan, Xiaohui [State Key Laboratory Cultivation Base for Nonmetal Composites and Functional Materials, Southwest University of Science and Technology, Mianyang 621010 (China); Zhou, Yong [Eco-materials and Renewable Energy Research Center (ERERC), School of Physics, National Lab of Solid State Microstructure, ERERC, Nanjing University, Nanjing 210093 (China); Pei, Chonghua, E-mail: [State Key Laboratory Cultivation Base for Nonmetal Composites and Functional Materials, Southwest University of Science and Technology, Mianyang 621010 (China)


    Highlights: • The NGO was synthesized by nitrifying homemade GO. • The N content of resulted NGO is up to 1.45 wt.%. • The NGO can facilitate the decomposition of AP and release much heat. - Abstract: Nitrated graphene oxide (NGO) was synthesized by nitrifying homemade GO with nitro-sulfuric acid. Fourier transform infrared spectroscopy (FTIR), laser Raman spectroscopy, CP/MAS {sup 13}C NMR spectra and X-ray photoelectron spectroscopy (XPS) were used to characterize the structure of NGO. The thickness and the compositions of GO and NGO were analyzed by atomic force microscopy (AFM) and elemental analysis (EA), respectively. The catalytic effect of the NGO for the thermal decomposition of ammonium perchlorate (AP) was investigated by differential scanning calorimetry (DSC). Adding 10% of NGO to AP decreases the decomposition temperature by 106 °C and increases the apparent decomposition heat from 875 to 3236 J/g.

  14. Size and Shape of Ammonium Perchlorate and their Influence on Properties of Composite Propellant

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    Sunil Jain


    Full Text Available Most of the composite propellant compositions contain solid loading up to 86 per cent. The main solid ingredients of composite propellant are ammonium perchlorate (AP and aluminium powder. Therefore, it is a must to characterise these to improve processibility and quality of composite propellant. Effect of particle size on propellants slurry viscosity and ballistic parameters are well documented, however, the effect of oxidizer particle shape is not reported. In the present study, different methods for size and shape characterisation are discussed and effect of size and shape of AP on composite propellant properties are studied. The data indicate that as size of AP decreases, propellant slurry viscosity increases and burn rate increases. The particles having higher shape factor provides less endof mix (EOM viscosity of propellant slurry and burn rate. Further, effect of size of ground AP on shape is also investigated. From the data thus obtained, it is inferred that as size of ground AP decreases, shape factor decreases, and particles become more irregular in shape.Defence Science Journal, 2009, 59(3, pp.294-299, DOI:

  15. Combustion Characteristics and Propulsive Performance of Boron/Ammonium Perchlorate Mixtures in Microtubes (United States)

    Liang, Daolun; Liu, Jianzhong; Zhou, Junhu; Wang, Yang; Yang, Yuxin


    A microthruster is used for the operation tracking and posture control of microsatellites. In this work, the combustion characteristics and propulsive performance of a boron/ammonium perchlorate (B/AP) propellant mixture for a microthruster were investigated. Amorphous B and AP were used in different mass ratios to prepare the propellant samples. A laser-ignition solid micropropulsion test system was set up, and a differential scanning calorimeter was used. The solid combustion products of the samples with good performance were collected. Microstructural and component analyses of the combustion products were performed. Various performance parameters, including the combustion temperature, combustion velocity, spectral intensity, ignition delay time, thrust, specific impulse, density specific impulse, and heat flow, changed with the fuel-oxidant ratio. The optimal fuel-oxidant mass ratio of the propellant samples was 40%, with a density specific impulse of 0.474 kg/m2•s and a maximum heat flow of 4.4913 mW/mg. Analysis of the combustion products revealed that the clearance between particles significantly diminished after combustion. During combustion, the AP completely decomposed, and a large amount of H3BO3, B2O3, and HBO2 was generated.

  16. Biomarker expression in lung of rabbit with pulmonary fibrosis induced by ammonium perchlorate. (United States)

    Wu, Feng-hong; Guo, Hui-xia; Lin, Ming-fang; Chen, Zhi-ze; Zhou, Xuan; Peng, Kai-liang


    Ammonium perchlorate (AP), an oxidizer, has been used in solid propellants. Although AP exposure has been suspected as a risk factor for the development of pulmonary fibrosis, data are still inconclusive. To evaluate the pulmonary toxicity and the potential pulmonary fibrosis caused by occupational exposure to this compound, 25 male rabbits were randomly allocated into five groups to receive AP or bleomycin or saline by intratracheal injection. All rabbits were sacrificed and total RNA from the lungs was extracted. Expressions of types I and III collagens, transforming growth factor-β(1) (TGF-β(1)) and tumour necrosis factor-α (TNF-α) messenger RNA (mRNA) were measured by reverse transcription-polymerase chain reaction (RT-PCR). The expressions of type I and III collagen mRNA in low, moderate and high dose AP groups were significantly higher (p < 0.01 or p < 0.05) than that in the saline group. There was also a significant increased level of TGF-β(1) and TNF-α mRNA in the three AP groups compared with saline control group (p < 0.01 or p < 0.05). These results reveal that AP can increase gene expressions of types I, III collagens, TGF-β(1) and TNF-α in lung of rabbits exposed to AP. The overexpression of these biomarkers were considered as effective indicator linking to the development of pulmonary fibrosis and finally demonstrated that AP has potential to induce pulmonary fibrosis.

  17. Effect of Surface Microstructure on the Temperature sensitivity of Burning Rate of Ammonium Perchlorate

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    K. Kishore


    Full Text Available Considering Vielle's law and the new thermodynamic model which the authors have developed recently the true dependence of temperature sensitivity of burning rate of ammonium perchlorate (AP on pressure is resolved and experimentally verified for bellet burning. The value of decreases with pressure steeply in regime I' (below 20 atm, but gently in regime I (above 20 atm. The value of powder AP has been determined and it is observed that (powder > (pellet, which clearly suggests that of is innuenced by the surface temperature sensitive parameter and hence by the surface/subsurface microstructure. In powder burning, the buoyant lifting of the particles into the gas phase occurs, Which constitutes the so-called 'free board region' (FER extending just above the true surface. Consequent to the decomposition of AP particles in FER, the condensed phase heat release gets curtailed and (powder becomes larger. A general relationship for in terms of density and surface temperature is suggested, which is applicable to both pellet and powder AP.

  18. The influence of VO2(B nanobelts on thermal decomposition of ammonium perchlorate

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    Zhang Yifu


    Full Text Available The influence of vanadium dioxide VO2(B on thermal decomposition of ammonium perchlorate (AP has not been reported before. In this contribution, the effect of VO2(B nanobelts on the thermal decomposition of AP was investigated by the Thermo- Gravimetric Analysis and Differential Thermal Analysis (TG/DTA. VO2(B nanobelts were hydrothermally prepared using peroxovanadium (V complexes, ethanol and water as starting materials. The thermal decomposition temperatures of AP in the presence of I wt.%, 3 wt.% and 6 wt.% of as-obtained VO2

  19. Study of the Deposition of Ammonium Perchlorate Following the Static Firing of MK-58 Rocket Motors (United States)


    hyperthyroidism , gas generators, electrolytes for lithium cells, and as chemical reagents. The occurrence of perchlorate in the environment is... treatments for the remediation of perchlorate in the environment (Refs. 10, 11). The debate on the acceptable levels of perchlorate in drinking...Biodegradation for Water Treatment ”, Environ. Sci. and Tecnol., Vol. 39 pp. 239A-247A, 2005. [11] Hatzinger, P.B., Whittier, C.M., Arkins, M.D., Bryan

  20. Evaluation of potassium iodide (KI) and ammonium perchlorate (NH4ClO4) to ameliorate 131I- exposure in the rat. (United States)

    Harris, C A; Fisher, J W; Rollor, E A; Ferguson, D C; Blount, B C; Valentin-Blasini, L; Taylor, M A; Dallas, C E


    Nuclear reactor accidents and the threat of nuclear terrorism have heightened the concern for adverse health risks associated with radiation poisoning. Potassium iodide (KI) is the only pharmaceutical intervention that is currently approved by the Food and Drug Administration for treating (131)I(-) exposure, a common radioactive fission product. Though effective, KI administration needs to occur prior to or as soon as possible (within a few hours) after radioactive exposure to maximize the radioprotective benefits of KI. During the Chernobyl nuclear reactor accident, KI was not administered soon enough after radiation poisoning occurred to thousands of people. The delay in administration of KI resulted in an increased incidence of childhood thyroid cancer. Perchlorate (ClO(4)(-)) was suggested as another pharmaceutical radioprotectant for 131I- poisoning because of its ability to block thyroidal uptake of iodide and discharge free iodide from the thyroid gland. The objective of this study was to compare the ability of KI and ammonium perchlorate to reduce thyroid gland exposure to radioactive iodide (131I-). Rats were dosed with 131I- tracer and 0.5 and 3 h later dosed orally with 30 mg/kg of either ammonium perchlorate or KI. Compared to controls, both anion treatments reduced thyroid gland exposure to 131I- equally, with a reduction ranging from 65 to 77%. Ammonium perchlorate was more effective than stable iodide for whole-body radioprotectant effectiveness. KI-treated animals excreted only 30% of the (131)I(-) in urine after 15 h, compared to 47% in ammonium perchlorate-treated rats. Taken together, data suggest that KI and ammonium perchlorate are both able to reduce thyroid gland exposure to 131I- up to 3 h after exposure to 131I-. Ammonium perchlorate may offer an advantage over KI because of its ability to clear 131I- from the body.

  1. Preparation of Nano-MnFe2O4 and Its Catalytic Performance of Thermal Decomposition of Ammonium Perchlorate

    Institute of Scientific and Technical Information of China (English)

    韩爱军; 廖娟娟; 叶明泉; 李燕; 彭新华


    Nano-MnFe2O4 particles were synthesized by co-precipitation phase inversion method and low-temperature combustion method respectively, using MnCl2, FeCl3, Mn(NO3)2, Fe(NO3)3, NaOH and C6H8O7. X-ray diffraction (XRD), transmission electron microscope (TEM), Fourier transform infrared spectroscopy (FT-IR), thermogravim-etry-differential thermal analysis (TG-DTA) and differential scanning calorimetry (DSC) were used to characterize the structure, morphology, thermal stability of MnFe2O4 and its catalytic performance to ammonium perchlorate. Results showed that single-phased and uniform spinel MnFe2O4 was obtained. The average particle size was about 30 and 20 nm. The infrared absorption peaks appeared at about 420 and 574 cm-1, and the particles were stable below 524 ℃. Using the two prepared catalysts, the higher thermal decomposition temperature of ammonium perchlorate was decreased by 77.3 and 84.9 ℃ respectively, while the apparent decomposition heat was increased by 482.5 and 574.3 J?g?1. The catalytic mechanism could be explained by the favorable electron transfer space provided by outer d orbit of transition metal ions and the high specific surface absorption effect of MnFe2O4 particles.

  2. Synthesis of polycrystalline Co{sub 3}O{sub 4} nanowires with excellent ammonium perchlorate catalytic decomposition property

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    Zhou, Hai [State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Lv, Baoliang, E-mail: [State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001 (China); Wu, Dong; Xu, Yao [State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001 (China)


    Graphical abstract: Co{sub 3}O{sub 4} nanowires with excellent ammonium perchlorate catalytic decomposition property were synthesized via a methanamide-assisted hydrolysis and subsequent dissolution–recrystallization process in the presence of methanamide. - Abstract: Co{sub 3}O{sub 4} nanowires, with the length of tens of micrometers and the width of several hundred nanometers, were produced by a hydrothermal treatment and a post-anneal process. X-ray diffraction (XRD) result showed that the Co{sub 3}O{sub 4} nanowires belong to cubic crystal system. Scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) analysis indicated that the Co{sub 3}O{sub 4} nanowires, composed by single crystalline nanoparticles, were of polycrystalline nature. On the basis of time-dependent experiments, methanamide-assisted hydrolysis and subsequent dissolution–recrystallization process were used to explain the precursors' formation process of the polycrystalline Co{sub 3}O{sub 4} nanowires. The TGA experiments showed that the as-obtained Co{sub 3}O{sub 4} nanowires can catalyze the thermal decomposition of ammonium perchlorate (AP) effectively.

  3. The Effects of Ammonium Perchlorate on Reproduction and Development of Amphibians (United States)


    magnesium [Mg], potassium, and sodium) on early amphibian development have shown that they, and AP in particular, are embryotoxic and significantly...testing, a range-finding test for KI was conducted to determine its embryotoxicity . Task 3: Effects of Perchlorate Derived from Food Sources on

  4. Synthesis of chrysalis-like CuO nanocrystals and their catalytic activity in the thermal decomposition of ammonium perchlorate

    Indian Academy of Sciences (India)

    Jun Wang; Shanshan He; Zhanshuang Li; Xiaoyan Jing; Milin Zhang; Zhaohua Jiang


    Chrysalis-like morphologies of CuO have been synthesized in large-quantity via a simple chemical deposition method without the use of any complex instruments and reagents. CuO nanocrystals showed a different morphology at three different temperatures, 25, 60 and 100°C. The particle size, morphology and crystal structure of the samples were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD) and Raman spectra. The catalytic effect of CuO nanoparticles on the decomposition of ammonium perchlorate (AP) was investigated by STA 409 PC thermal analyzer at a heating rate of 10°C min-1 from 35 to 500°C. Compared with the thermal decomposition of pure AP, the addition of CuO nanoparticles decreased the decomposition temperature of AP by about 85°C.

  5. Limited overshooting of NH{sub 4}{sup +} ions in ammonium perchlorate; Ograniczene przeskoki jonow NH{sub 4}{sup +} w nadchloranie amonowym

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    Birczynski, A.; Lalowicz, Z.T. [Inst. of Nuclear Physics, Cracow (Poland); Ingman, L.P.; Punkkinen, M.; Ylinen, E.E. [Wihuri Physical Lab., Turku Univ., Turku (Finland)


    The interpretation of NMR spectra for polycrystalline sample of ammonium perchlorate in helium temperature assumes the tunneling of NH{sub 4}{sup +}. Such interpretation does not agree with experimental data. The hypothesis of additional motion (fast rotation around one of C3 axis) has been checked and discussed on the base of NMR spectra of NH{sub 4}ClO{sub 4} monocrystal for the temperature range 2.1-25 K. 9 refs, 1 fig.

  6. Sol–gel method to prepare graphene/Fe{sub 2}O{sub 3} aerogel and its catalytic application for the thermal decomposition of ammonium perchlorate

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    Lan, Yuanfei; Li, Xiaoyu; Li, Guoping; Luo, Yunjun, E-mail: [Beijing Institute of Technology, School of Materials Science and Engineering (China)


    Graphene/Fe{sub 2}O{sub 3} (Gr/Fe{sub 2}O{sub 3}) aerogel was synthesized by a simple sol–gel method and supercritical carbon dioxide drying technique. In this study, the morphology and structure were characterized by scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, X-ray diffraction, and nitrogen sorption tests. The catalytic performance of the as-synthesized Gr/Fe{sub 2}O{sub 3} aerogel on the thermal decomposition of ammonium perchlorate (AP) was investigated by thermogravimetric and differential scanning calorimeter. The experimental results showed that Fe{sub 2}O{sub 3} with particle sizes in the nanometer range was anchored on the Gr sheets and Gr/Fe{sub 2}O{sub 3} aerogel exhibits promising catalytic effects for the thermal decomposition of AP. The decomposition temperature of AP was obviously decreased and the total heat release increased as well.

  7. Synthesis and characterization of an energetic compound Cu(Mtta)2(NO3)2 and effect on thermal decomposition of ammonium perchlorate. (United States)

    Yang, Qi; Chen, Sanping; Xie, Gang; Gao, Shengli


    An energetic coordination compound Cu(Mtta)(2)(NO(3))(2) has been synthesized by using 1-methyltetrazole (Mtta) as ligand and its structure has been characterized by X-ray single crystal diffraction. The central copper (II) cation was coordinated by four O atoms from two Mtta ligands and two N atoms from two NO(3)(-) anions to form a six-coordinated and distorted octahedral structure. 2D superamolecular layer structure was formed by the extensive intermolecular hydrogen bonds between Mtta ligands and NO(3)(-) anions. Thermal decomposition process of the compound was predicted based on DSC and TG-DTG analyses results. The kinetic parameters of the first exothermic process of the compound were studied by the Kissinger's and Ozawa-Doyle's methods. Sensitivity tests revealed that the compound was insensitive to mechanical stimuli. In addition, compound was explored as additive to promote the thermal decomposition of ammonium perchlorate (AP) by differential scanning calorimetry.

  8. Radioactive iodide (131 I-) excretion profiles in response to potassium iodide (KI) and ammonium perchlorate (NH4ClO4) prophylaxis. (United States)

    Harris, Curtis; Dallas, Cham; Rollor, Edward; White, Catherine; Blount, Benjamin; Valentin-Blasini, Liza; Fisher, Jeffrey


    Radioactive iodide ((131)I-) protection studies have focused primarily on the thyroid gland and disturbances in the hypothalamic-pituitary-thyroid axis. The objective of the current study was to establish (131)I- urinary excretion profiles for saline, and the thyroid protectants, potassium iodide (KI) and ammonium perchlorate over a 75 hour time-course. Rats were administered (131)I- and 3 hours later dosed with either saline, 30 mg/kg of NH(4)ClO(4) or 30 mg/kg of KI. Urinalysis of the first 36 hours of the time-course revealed that NH(4)ClO(4) treated animals excreted significantly more (131)I- compared with KI and saline treatments. A second study followed the same protocol, but thyroxine (T(4)) was administered daily over a 3 day period. During the first 6-12 hour after (131)I- dosing, rats administered NH(4)ClO(4) excreted significantly more (131)I- than the other treatment groups. T(4) treatment resulted in increased retention of radioiodide in the thyroid gland 75 hour after (131)I- administration. We speculate that the T(4) treatment related reduction in serum TSH caused a decrease synthesis and secretion of thyroid hormones resulting in greater residual radioiodide in the thyroid gland. Our findings suggest that ammonium perchlorate treatment accelerates the elimination rate of radioiodide within the first 24 to 36 hours and thus may be more effective at reducing harmful exposure to (131)I- compared to KI treatment for repeated dosing situations. Repeated dosing studies are needed to compare the effectiveness of these treatments to reduce the radioactive iodide burden of the thyroid gland.

  9. Synthesis, Evaluation, and Formulation Studies on New Oxidizers as Alternatives to Ammonium Perchlorate in DoD Missile Propulsion Applications (United States)


    States Army Corps of Engineers, Waterways Experiment Station. Vicksburg, MS. Santhosh , G., S. Venkatachalam and K.N, Ninan. Adsorption of...October. Venkatachalam, S., S. Santhosh and K.N. Ninan. 2004. An overview on the synthetic routes and properties of ammonium dinitramide (AND) and

  10. 纳米级金属和金属复合物粉末对高氯酸铵和高氯酸铵/聚合丁二烯复合固体推进剂热分解特性的影响%Effects of Metal and Composite Metal Nanopowders on the Thermal Decomposition of Ammonium Perchlorate (AP) and the Ammonium Perchlorate/Hydroxyterminated Polybutadiene (AP/HTPB) Composite Solid Propellant

    Institute of Scientific and Technical Information of China (English)

    刘磊力; 李凤生; 谈玲华; 李敏; 杨毅


    Effects of metal (Ni, Cu, Al) and composite metal (NiB, NiCu, NiCuB) nanopowders on the thermal decomposition of ammonium perchlorate (AP) and composite solid propellant ammonium perchlorate/hydroxyterminated polybutadiene (AP/HTPB) were studied by thermal analysis (DTA). The results show that metal and composite metal nanopowders all have good catalytic effects on the thermal decomposition of AP and AP/HTPB composite solid propellant. The effects of metal nanopowders on the thermal decomposition of AP are less than those of the composite metal nanopowders. The effects of metal and composite metal nanopowders on the thermal decomposition of AP are different from those on the thermal decomposition of the AP/HTPB composite solid propellant.

  11. Pure CuCr2O4 nanoparticles: Synthesis, characterization and their morphological and size effects on the catalytic thermal decomposition of ammonium perchlorate (United States)

    Hosseini, Seyed Ghorban; Abazari, Reza; Gavi, Azam


    In the present paper a pure phase of the copper chromite spinel nanoparticles (CuCr2O4 SNPs) were synthesized via the sol-gel route using citric acid as a complexing agent. Then, the CuCr2O4 SNPs has been characterized by field emission scanning electron microscope (FE-SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD). In the next step, with the addition of Cu-Cr-O nanoparticles (NPs), the effects of different parameters such as Cu-Cr-O particle size and the Cu/Cr molar ratios on the thermal behavior of Cu-Cr-O NPs + AP (ammonium perchlorate) mixtures were investigated. As such, the catalytic effect of the Cu-Cr-O NPs for thermal decomposition of AP was evaluated by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). TGA/DSC results showed that the samples with different morphologies exhibited different catalytic activity in different stages of thermal decomposition of AP. Also, in the presence of Cu-Cr-O nanocatalysts, all of the exothermic peaks of AP shifted to a lower temperature, indicating the thermal decomposition of AP was enhanced. Moreover, the heat released (ΔH) in the presence of Cu-Cr-O nanocatalysts was increased to 1490 J g-1.

  12. Hydrothermal preparation of Fe{sub 2}O{sub 3}/graphene nanocomposite and its enhanced catalytic activity on the thermal decomposition of ammonium perchlorate

    Energy Technology Data Exchange (ETDEWEB)

    Yuan, Yuan [National Special Superfine Powder Engineering Research Center, Nanjing University of Science and Technology, Nanjing 210094 (China); Jiang, Wei, E-mail: [National Special Superfine Powder Engineering Research Center, Nanjing University of Science and Technology, Nanjing 210094 (China); Wang, Yujiao; Shen, Ping; Li, Fengsheng; Li, Pingyun [National Special Superfine Powder Engineering Research Center, Nanjing University of Science and Technology, Nanjing 210094 (China); Zhao, Fengqi; Gao, Hongxu [Xi’an Modern Chemistry Research Institute, Xi’an 710065 (China)


    Fe{sub 2}O{sub 3}/graphene nanocomposite was prepared by a facile hydrothermal method, during which graphene oxides (GOs) were reduced to graphene with hydrazine and Fe{sub 2}O{sub 3} nanoparticles were simultaneously anchored on graphene sheets. The morphology of the obtained Fe{sub 2}O{sub 3}/graphene nanocomposite was investigated by scanning electron microscopy (SEM) and transmission electron microscope (TEM). It was revealed by TEM images that Fe{sub 2}O{sub 3} nanoparticles grew well on the surfaces of graphene. As much as I know, this new nanocomposite has not been investigated as a catalyst on the thermal decomposition of AP yet. In this work, the catalytic performance of the synthesized material on the thermal decomposition of ammonium perchlorate (AP) was investigated creatively by differential scanning calorimetry (DSC). The results of DSC indicated that graphene obviously improved the catalytic activity of Fe{sub 2}O{sub 3} on the thermal decomposition of AP due to its high specific area.

  13. Preparation of Coaxial-Line and Hollow Mn2O3 Nanofibers by Single-Nozzle Electrospinning and Their Catalytic Performances for Thermal Decomposition of Ammonium Perchlorate. (United States)

    Liang, Jiyuan; Yang, Jie; Cao, Weiguo; Guo, Xiangke; Guo, Xuefeng; Ding, Weiping


    Coaxial-line and hollow Mn2O3 nanofibers have been synthesized by a simple single-nozzle electrospinning method without using a complicated coaxial jet head, combined with final calcination. The crystal structure and morphology of the Mn2O3 nanofibers were investigated by using the X-ray diffraction, scanning electron microscopy and transmission electron microscopy. The results indicate that the electrospinning distance has important influence on the morphology and structure of the obtained Mn2O3 nanofibers, which changes from hollow fibers for short electrospinning distance to coaxial-line structure for long electrospinning distance after calcination in the air. The formation mechanisms of different structured Mn2O3 fibers are discussed in detail. This facile and effective method is easy to scale up and may be versatile for constructing coaxial-line and hollow fibers of other metal oxides. The catalytic activity of the obtained Mn2O3 nanofibers on thermal decomposition of ammonium perchlorate (AP) was studied by differential scanning calorimetry (DSC). The results show that the hollow Mn2O3 nanofibers have good catalytic activity to promote the thermal decomposition of AP.

  14. Green synthesis of Co{sub 3}O{sub 4} nanoparticles and their applications in thermal decomposition of ammonium perchlorate and dye-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, J.K. [Department of Chemistry, Deen Dayal Upadhyay Gorakhpur University, Gorakhpur (India); Srivastava, Pratibha, E-mail: [Department of Chemistry, Deen Dayal Upadhyay Gorakhpur University, Gorakhpur (India); Singh, Gurdip [Department of Chemistry, Deen Dayal Upadhyay Gorakhpur University, Gorakhpur (India); Akhtar, M. Shaheer [New & Renewable Energy Material Development Center (NewREC), Chonbuk National University, Jeonbuk (Korea, Republic of); Ameen, S. [Energy Materials & Surface Science Laboratory, Solar Energy Research Center, School of Chemical Engineering, Chonbuk National University, Jeonju 561-756 (Korea, Republic of)


    Graphical abstract: - Highlights: • Co{sub 3}O{sub 4} NPs were synthesized from the leaves extract of plant Calotropis gigantea. • Green synthesis of Co{sub 3}O{sub 4} NPs is a cost effective and eco-friendly route. • Faster thermal decomposition of AP occurred in presence of the green synthesized Co{sub 3}O{sub 4} NPs. • A high burning rate of CSP was observed. • Green synthesized Co{sub 3}O{sub 4} NPs displays the good electrocatalytic activity to reduction of I{sub 3}{sup −} to I{sup −} ions. - Abstract: In this paper, we report on the green synthesis of cobalt oxide nanoparticles (Co{sub 3}O{sub 4} NPs) using leaves extract of plant Calotropis gigantea and characterize by X-ray diffraction (XRD), UV–vis spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDX). The green synthesized Co{sub 3}O{sub 4} NPs showed excellent catalytic effect on the thermal decomposition of ammonium perchlorate (AP) and burning rate of composite solid propellants (CSPs). Kinetics of slow and rapid thermal decomposition has been investigated by isoconversional and ignition delay methods, respectively. Moreover, the electrocatalytic performance of green synthesized Co{sub 3}O{sub 4} NPs in dye-sensitized solar cells (DSSC) has also been evaluated. The cyclic voltametry measurement shows good electrocatalytic activity of Co{sub 3}O{sub 4} NPs toward the reduction of I{sub 3}{sup −} to I{sup −} ions.

  15. PERCHLORATE FACTS (United States)

    Perchlorate is an anion (negative ion) with the formula C1O 4-. Perchlorate salts are famous in inorganic chemistry on account of their high solubilities. As a result, they are very difficult to remove. Although hot and concentrated perchloric acid is a strong oxidizing agent,...

  16. Alternative Causes of Wide-Spread, Low Concentration Perchlorate Impacts to Groundwater (United States)


    substances such as titanium slags Acid digestion Ammonium perchlorate, high purity metal perchlorates Starting material for the manufacture of pure...ammonium perchlorate and in the production of high purity metal perchlorates Pickling and passivation of iron and steels Oxidant Determination of...Potassium Nitrate 13 White Sparks Potassium Perchlorate 42.1 Titanium 42.1 Dextrine 15.8 White Sparks “water fall” Potassium

  17. Environmental biotechnology and microbiology of (per)chlorate reducing bacteria

    NARCIS (Netherlands)

    Mehboob, F.; Schraa, G.; Stams, A.J.M.


    Perchlorates are the salts derived from perchloric acid (HClO4). They occur both naturally and through manufacturing. They have been used as a medicine for more than 50 years to treat thyroid gland disorders and are used extensively within the pyrotechnics industry, and ammonium perchlorate is also

  18. Ammonium Perchlorate Transportation Hazards Testing (United States)


    n1 t- TI T1W- r- T’ T II 0 0L 10 T. J II )0 In L11 n n i) ) C, (71 T-. d n 𔃺 ’ O 4j ’G134j L) ) 0 4j .1-10. 0 Il I-I 60 In 0 InI ni ni nini r , - r...n Q TIT a tf M L) QtQ0 O 4 4 0.14 3 41,31)-1 17 �’tIl 014 l’ 01 i. 0 - a. OC t. L 0I n nI nini n0ni nu n- n-r- rd Ifl 0n - 44 4 0o 3-00- 300- -TI

  19. Synthesis of Co Nanoparticles and Their Catalytic Effect on the Decomposition of Ammonium Perchlorate%纳米金属钴粒子的制备及对高氯酸铵热分解的影响

    Institute of Scientific and Technical Information of China (English)

    段红珍; 蔺向阳; 刘冠鹏; 徐磊; 李凤生


    The monodispersed Co nanoparticles were successfully prepared by means of hydrogen plasma method in inert atmosphere. The particle size, specific surface area, crystal structure and morphology of the samples were characterized by transmission electron microscopy (TEM), BET equation, X-ray diffraction (XRD), and the corre- sponding selected area electron diffraction (SAED). The catalytic effect of Co nanoparticles on the decomposition of ammonium perchlorate (AP) was investigated by differential thermal analyzer (DTA). Compared with the ther- mal decomposition of pure AP, the addition of Co nanoparticles (2%-10%, by mass) decreases the decomposition temperature of AP by 145.01-155.72℃. Compared with Co3O4 nanoparticles and microsized Co particles, the catalytic effect of Co nanoparticles for AP is stronger. Such effect is attributed to the large specific surface area and its interaction of Co with decomposition intermediate gases. The present work provides useful information for the application of Co nanoparticles in the AP-based propellant.

  20. Radioactive Iodide (131I Excretion Profiles in Response to Potassium Iodide (KI and Ammonium Perchlorate (NH4ClO4 Prophylaxis

    Directory of Open Access Journals (Sweden)

    Jeffrey Fisher


    Full Text Available Radioactive iodide (131I protection studies have focused primarily on the thyroid gland and disturbances in the hypothalamic-pituitary-thyroid axis. The objective of the current study was to establish 131I urinary excretion profiles for saline, and the thyroid protectants, potassium iodide (KI and ammonium perchlorate over a 75 hour time-course. Rats were administered 131I and 3 hours later dosed with either saline, 30 mg/kg of NH4ClO4 or 30 mg/kg of KI. Urinalysis of the first 36 hours of the time-course revealed that NH4ClO4 treated animals excreted significantly more 131I compared with KI and saline treatments. A second study followed the same protocol, but thyroxine (T4 was administered daily over a 3 day period. During the first 6–12 hour after 131I dosing, rats administered NH4ClO4 excreted significantly more 131I than the other treatment groups. T4 treatment resulted in increased retention of radioiodide in the thyroid gland 75 hour after 131I administration. We speculate that the T4 treatment related reduction in serum TSH caused a decrease synthesis and secretion of thyroid hormones resulting in greater residual radioiodide in the thyroid gland. Our findings suggest that ammonium perchlorate treatment accelerates the elimination rate of radioiodide within the first 24 to 36 hours and thus may be more effective at reducing harmful exposure to 131I compared to KI treatment for repeated dosing situations. Repeated dosing studies are needed to compare the effectiveness of these treatments to reduce the radioactive iodide burden of the thyroid gland.

  1. A Skeletal, Gas Phase, Finite Rate, Chemical Kinetics Mechanism for Modeling the Deflagration of Ammonium Perchlorate - Hydroxyl-Terminated Polybutadiene Composite Propellants (United States)


    expressions that sensitivity analyses indicated were important. Addressing this issue through the application of computational - chemistry -based methods...Lin MC. Computational studies on the kinetics and mechanisms for NH3 reactions with ClOx (x = 0 - 4) radicals. Journal of Physical Chemistry A...ABSTRACT A (full) detailed, gas-phase, finite-rate chemical kinetics mechanism for representing the combustion- chemistry -associated ammonium


    Ammonium Perchlorate (AP) is produced on a large scale by the chemical industry, for a wide range of applications for example, as a strong oxidizing agent in solid rocket fuel. AP must be washed out of the inventory periodically due to its limited shelf-life,and replaced with a f...

  3. Environmental Screening Assessment of Perchlorate Replacements (United States)


    nitramido)dinitroethylene AP Ammonium perchlorate CAS Chemical Abstract Services DNNC 1,3,5,5-tetranitrohexahydropyrimidine EPI Estimation Program...can be created and pasted into the input screen or obtained from a linked file of Chemical Abstract Services (CAS) numbers. The EPI Suite Interface

  4. Catalytic behaviors of CoB and CoB/SiO2 in thermal decomposition of ammonium perchlorate%CoB和CoB/SiO2对AP热分解的催化活性研究

    Institute of Scientific and Technical Information of China (English)

    李茸; 刘祥萱; 王煊军


    Silicon-supported cobalt-boron(CoB/SiO2) and cobalt-boron (CoB) nano-sized catalysts were synthesized via chemical deposition method. Their catalytic behavior in the thermal decomposition of ammonium perchlorate( AP) was briefly studied by thermo-gravimetric and differential thermal analysis (TG-DTA). Results show that both CoB/SiO2 and CoB have catalytic effects on the thermal decomposition of AP. CoB/SiO2 is more effective. The high-temperature thermal decomposition temperature of AP was decreased by 166. 2 ℃ with the addition of 5% CoB/SiO2. This effect is mainly attributed to its higher thermodynamic stability compared with CoB,whch is favorable for catalysis.%采用化学沉积方法,制备了纳米尺度CoB和SiO2·负载的CoB/SiO2催化剂.通过热重-差热分析(TG-DTA)实验,研究了催化剂在AP热分解过程中的催化性能.结果表明,CoB和CoB/SiO2对AP热分解均表现出催化活性,CoB/SiO2的活性更强;质量分数5%的CoB/SiO2,可将AP高温热分解峰的峰温降低166.2℃;CoB/SiO2较好的催化效果,归因于其相对CoB更高的热力学稳定性;负载型催化剂的较高热力学稳定性,更有利于其催化活性的履行.

  5. 高氯酸铵/石墨烯纳米复合材料的制备及热分解行为%Preparation and Thermal Decomposition Behaviour of Ammonium Perchlorate/Graphene Aerogel Nanocomposites

    Institute of Scientific and Technical Information of China (English)

    王学宝; 李晋庆; 罗运军


    通过溶胶-凝胶法制备了高氯酸铵/石墨烯气凝胶(AP/GA)纳米复合材料,用SEM、元素分析和XRD对其结构进行了表征,用TG-DSC-IR联用技术对其热分解行为进行了研究.结果表明,AP/GA纳米复合材料中,AP以纳米尺寸存在于石墨烯气凝胶中,AP质量分数高达94.4%,平均粒径约为69.41 nm.石墨烯对AP的热分解过程具有明显的催化作用,与AP相比,AP/GA纳米复合材料的低温分解峰消失,高温分解峰温降低了83.7℃.总分解热达2110J/g.%Ammonium perchlorate / graphene aerogels (AP/GA) nanocomposites were prepared by sol-gel method and characterized by scanning electron microscope(SEM), elemental analysis and X-ray diffraction(XRD). Their thermal decomposition behaviours were investigated by TG-DSC-IR. The results indicate that AP is presented in the AP/GA nanocomposites with an average particle size of 69. 41 nm and occupied 94. 4 % of total mass. GA shows an obvious catalytic effect on the thermal decomposition of AP/GA. Compared to pure AP, the low temperature decomposition peak of AP/GA nanocomposites disappears, the high temperature decomposition peak temperature decreases by 83. 7℃ , and the total heat release reaches 2110 J/g.

  6. High-Nitrogen-Based Pyrotechnics: Development of Perchlorate-Free Green-Light Illuminants for Military and Civilian Applications (United States)


    become a concern of the US Department of Defense is the “perchlorate issue.” Potassium perchlorate and ammonium perchlorate oxidizers, once believed to be...amongst ideal oxi- dizers owing to their inherent reactivity, stability , low cost, low hygroscopicity, and large positive oxygen balances, have now...groundwater, thus posing a po- tential risk to drinking supplies. Perchlorates are believed to be teratogenic and the anion is believed to compete with iodide

  7. Preparation of nanometer NiO/MgO and its catalytic performance for thermal decomposition of ammonium perchlorate%纳米NiO/MgO的制备及其对AP热分解催化性能影响

    Institute of Scientific and Technical Information of China (English)

    谈玲华; 李勤华; 杭祖圣; 潘仁明; 姜炜; 李凤生


    采用浸渍法制备出纳米NiO/MgO复合氧化物粒子,运用X射线衍射(XRD)、X射线能谱仪(EDS)等对产物的物相和组成进行了表征,并研究了单一纳米粒子(NiO、MgO)、纳米NiO+MgO混合粒子及纳米NiO/MgO复合氧化物粒子对AP热分解的催化性能.结果表明,所制备的纳米NiO/MgO复合氧化物粒子中NiO粒子高度分散于MgO载体中.纳米NiO/MgO复合氧化物粒子可使AP的高温分解峰温降低92.2℃,高低温分解峰温差减小到10.6℃,表现出较强的催化性能,其催化性能优于单一纳米粒子(NiO、MgO)、纳米NiO+MgO混合粒子.纳米MgO的载体支撑作用,可防止NiO纳米粒子的团聚,增加反应活性中心,从而提高催化效果.%The nanometer NiO/MgO composite particles were prepared via impregnation method. The phase and morphology of NiO/MgO composites were characterized by X-ray diffraction, transmission electron microscopy and energy dispersive X-Ray spectroscopy. The catalysis of nanometer particles ( NiO, MgO), NiO + MgO mixture particles and NiO/MgO composite particles the thermal decomposition of ammonium perchlorate (AP) was investigated by DSC. The Results show that NiO particles are highly dispersed on the MgO support. Catalytic performance of the obtained nanometer NiO/MgO composite particles is superior to that of corresponding single ingredient and NiO + MgO mixture particles. Nanometer NiO/MgO can make the high-temperature decomposition peak value of AP decrease by 92.2 ℃ and the temperature difference value between the low and high temperature decomposition peak reduce up to 10. 6 ℃, which indicates good catalytic performance. The supporting effect of the nanometer MgO can effectively prevent the aggregation of NiO particles and increase the active sites.

  8. Health survey of plant workers for an occupational exposure to ammonium perchlorate%某化工厂过氯酸铵粉尘作业工人健康状况调查

    Institute of Scientific and Technical Information of China (English)

    陈红霞; 邵元鹏; 巫丰宏; 李艳萍; 彭开良


    目的 了解过氯酸铵(AP)粉尘对作业工人健康的影响,为其预防措施提供依据.方法 选择该厂接触AP粉尘的36名作业工人为接触组,不接触AP粉尘的48名该厂工人为对照组.调查工厂的一般情况,监测作业场所的AP粉尘浓度,对两组人群进行职业健康体检,检测血常规、肝肾功能、甲状腺激素指标,进行肺通气功能和X线胸片检查.结果 AP总粉尘浓度以组批车间最高,为(51.63±43.27) mg/m3.接触组收缩压[(146.14±21.03)mmHg]明显高于对照组[(134.67±18.58)mmHg],差异有统计学意义(P<0.05).接触组全身各系统症状(皮粗、皮痒、气短、咳嗽、咳痰、咽干、疲乏无力等)累计检出率、气短及皮痒的检出率分别为86.11%、30.56%、36.11%,均明显高于对照组(66.67%、12.50%、10.42%),差异均有统计学意义(P<0.05).接触组的游离三碘甲状腺原氨酸(FT3)水平[(1.29±0.20) ng/ml]明显低于对照组[(1.41±0.23) ng/ml],差异有统计学意义(P<0.01).接触组工人的1秒用力肺活量与用力肺活量百分比值(FEV1.0/FVC)低于对照组,但差异无统计学意义(P>0.05).接触组检出1例肺部X线影像异常者,并诊断为尘肺,对照组检出1例左肺门区有1约1.0x1.0小结节影.结论 接触组工人的收缩压明显高于对照组,不排除与接触AP粉尘有关;接触组工人的FT3低于对照组,提示长期接触AP粉尘可能会对作业工人甲状腺功能造成影响.%Objective To understand the occupational hazards of ammonium perchlorate dust on operating workers and to provide the basis preventive measures for protecting the workers' health.Methods 36 workers exposed to ammonium perchlorate dust and 48 unexposed workers from one factory were selected as the exposure and control groups.Investigations on the general condition,sampling of dust in the workplaces and a special medical examination were conducted for two groups,including occupational history

  9. Perchlorate isotope forensics (United States)

    Böhlke, J.K.; Sturchio, N.C.; Gu, B.; Horita, J.; Brown, G.M.; Jackson, W.A.; Batista, J.; Hatzinger, P.B.


    Perchlorate has been detected recently in a variety of soils, waters, plants, and food products at levels that may be detrimental to human health. These discoveries have generated considerable interest in perchlorate source identification. In this study, comprehensive stable isotope analyses ( 37Cl/35Cl and 18O/17O/ 16O) of perchlorate from known synthetic and natural sources reveal systematic differences in isotopic characteristics that are related to the formation mechanisms. In addition, isotopic analyses of perchlorate extracted from groundwater and surface water demonstrate the feasibility of identifying perchlorate sources in contaminated environments on the basis of this technique. Both natural and synthetic sources of perchlorate have been identified in water samples from some perchlorate occurrences in the United States by the isotopic method. ?? 2005 American Chemical Society.

  10. Interaction between perchlorate and iodine in the metamorphosis of Hyla versicolor (United States)

    Sparling, D.W.; Harvey, G.; Nzengung, V.; Linder, Gregory L.; Krest, Sherry K.; Sparling, Donald W.; Little, Edward E.


    Perchlorate (ClO4-) is a water-soluble, inorganic anion that is often combined with ammonium, potassium or other cations for use in industry and agriculture. Ammonium perchlorate, for example, is a potent oxidizer and is used in various military applications including rocket fuel. It has also been found in an historically widely used fertilizer, Chilean nitrate and in other fertilizers. It has been found in ground and surface waters of over 30 states and is considered a human health risk. Because of its similar atomic radius and volume, perchlorate competes with iodide for thyroid uptake and storage and thereby inhibits production of thyroid hormones. Amphibians may be particularly affected by perchlorate because they rely on the thyroid for metamorphosis. This study exposed early larval Hyla versicolor to concentrations of perchlorate ranging from 2.2 to 50 ppm to determine the effects of perchlorate on a native amphibian. In addition, three controls, 0 perchlorate, 0 perchlorate with 0.10 ppm iodide (C + I) and 50 ppm perchlorate + 0.10 ppm iodide (50 + I) were tested. Mortality (<11% with all treatments) and growth appeared to be unaffected by perchlorate. Inhibition of development started with 2.2 ppm perchlorate and little or no development occurred at 22.9 ppm and above. This inhibition was particularly apparent at the latter stages of development including hindlimb formation and metamorphosis. The estimated EC50 for total inhibition of metamorphosis at 70 days of treatment was 3.63 ppm. There was no evidence of inhibition of development with the 50 + I, C + I, or controls, indicating that the presence of small concentrations of iodide could counter the effects of perchlorate. When tadpoles that had been inhibited by perchlorate were subsequently treated with iodide, development through prometamorphosis progressed but mortality was very high.

  11. Exposure to perchlorate induces the formation of macrophage aggregates in the trunk kidney of zebrafish and mosquitofish (United States)

    Capps, T.; Mukhi, S.; Rinchard, J.J.; Theodorakis, C.W.; Blazer, V.S.; Patino, R.


    Environmental contamination of ground and surface waters by perchlorate, derived from ammonium perchlorate (AP) and other perchlorate salts, is of increasing concern. Exposure to perchlorate can impair the thyroid endocrine system, which is thought to modulate renal and immune function in vertebrates. This study with zebrafish Danio rerio and eastern mosquitofish Gambusia holbrooki examined the histological effects of perchlorate on the trunk kidney, which in teleosts serves excretory and hemopoietic functions and therefore may be a target of perchlorate effects. Adult zebrafish of both sexes were exposed in the laboratory to waterborne, AP-derived perchlorate at measured concentrations of 18 mg/L for 8 weeks. Adult male mosquitofish were exposed to waterborne sodium perchlorate at measured perchlorate concentrations of 1-92 mg/L for 8 weeks. Control fish were kept in untreated water. The region of the body cavity containing the trunk kidney was processed from each fish for histological analysis. Macrophage aggregates (MAs), possible markers of contaminant exposure or immunotoxic effect, were present in the hemopoietic region of the kidney in both species exposed to perchlorate. The estimated percent area of kidney sections occupied by MAs was greater in zebrafish exposed to perchlorate at 18 mg/L (P kidney is affected by exposure to perchlorate. The concentrations of perchlorate at which the effects were noted are relatively high but within the range reported in some contaminated habitats.

  12. Perchlorate Questions and Answers (United States)

    ... Dietary Intake of Perchlorate and Iodine" in the Journal of Exposure Science and Environmental Epidemiology. This study reports on the ... Compliance Federal, State & Local Officials Consumers Health Professionals ... Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products

  13. Widespread Occurrence of Plant Perchlorate (United States)

    Harvey, G.; Orris, G.; Jackson, W. A.; Rajagopalan, S.; Andraski, B.; Stonestrom, D.


    Perchlorate is a water soluble oxyanion containing four oxygens bonded to a single chlorine atom. High concentration of perchlorate can competitively block the uptake of iodide by the sodium iodide symporter and disrupt thyroid function. Due to this ability to potentially impair thyroid function, perchlorate in environmental exposure pathways has been of concern for more than a decade. Our knowledge of the spatial and temporal aspects of environmental perchlorate has increased dramatically in the past few years. To date, perchlorate has been found in numerous different environmental media, including water, soils and sediments, and plants, from many parts of the world. Perchlorate can be found in marine alage, food and plant samples from Asia, Africa, Europe, North and South America. It is becoming increasingly apparent that perchlorate in low levels is ubiquitous. Perchlorate has been found in several different carbon age-dated water and midden samples that pre-date the industrial age and agricultural use of Chilean nitrate fertilizers by thousands of years. While anthropogenic sources of perchlorate exist, the accumulating spatial and temporal evidence suggests that perchlorate must have a significant natural source. This natural source of perchlorate under the appropriate geochemical and climatic conditions is contributing a natural background level of perchlorate. Concentrations of perchlorate in soils appears to be influenced by soil geochemistry. Soils with low organic content usually have higher levels of perchlorate then soils with abundant organic matter. High levels of perchlorate have been found in remotely located xerophytes growing in aridosols and in deciduous phreatophytes growing in humid densely populated areas. Often the amount of perchlorate in a plant cannot be explained by the amount of perchlorate in either the soil or precipitation. Investigations into the relative source contribution of lithogenic, atmospheric and other sources and mechanisms

  14. Bioelectrical Perchlorate Remediation (United States)

    Thrash, C.; Achenbach, L. A.; Coates, J. D.


    Several bioreactor designs are currently available for the ex-situ biological attenuation of perchlorate- contaminated waters and recently, some of these reactor designs were conditionally approved by the California Department of Health Services for application in the treatment of perchlorate contaminated drinking water. However, all of these systems are dependent on the continual addition of a chemical electron donor to sustain microbial activity and are always subject to biofouling and downstream water quality issues. In addition, residual labile electron donor in the reactor effluent can stimulate microbial growth in water distribution systems and contribute to the formation of potentially toxic trihalomethanes during disinfection by chlorination. As part of our ongoing studies into microbial perchlorate reduction we investigated the ability of dissimilatory perchlorate reducing bacteria (DPRB) to metabolize perchlorate using a negatively charged electrode (cathode) in the working chamber of a bioelectrical reactor (BER) as the primary electron donor. In this instance the DPRB use the electrons on the electrode surface either directly or indirectly in the form of electrolytically produced H2 as a source of reducing equivalents for nitrate and perchlorate reduction. As part of this investigation our fed-batch studies showed that DPRB could use electrons from a graphite cathode poised at -500mV (vs. Ag/AgCl) for the reduction of perchlorate and nitrate. We isolated a novel organism, Dechlorospirillum strain VDY, from the cathode surface after 70 days operation which readily reduced 100 mg.L-1 perchlorate in a mediatorless batch bioelectrical reactor (BER) in 6 days. Continuous up-flow BERs (UFBERs) seeded with active cultures of strain VDY continuously treated waters containing 100 mg.L-1 perchlorate with almost 100% efficiency throughout their operation achieving a non-optimized volumetric loading of 60 mg.L-1 reactor The same UFBERs also treated

  15. Detoxification of PAX-21 ammunitions wastewater by zero-valent iron for microbial reduction of perchlorate. (United States)

    Ahn, Se Chang; Cha, Daniel K; Kim, Byung J; Oh, Seok-Young


    US Army and the Department of Defense (DoD) facilities generate perchlorate (ClO(4)(-)) from munitions manufacturing and demilitarization processes. Ammonium perchlorate is one of the main constituents in Army's new main charge melt-pour energetic, PAX-21. In addition to ammonium perchlorate, hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and 2,4-dinitroanisole (DNAN) are the major constituents of PAX-21. In order to evaluate microbial perchlorate reduction as a practical option for the treatment of perchlorate in PAX-21 wastewater, we conducted biodegradation experiments using glucose as the primary sources of electrons and carbon. Batch experiments showed that negligible perchlorate was removed in microbial reactors containing PAX-21 wastewater while control bottles containing seed bacteria and glucose rapidly and completely removed perchlorate. These results suggested that the constituents in PAX-21 wastewater may be toxic to perchlorate reducing bacteria. A series of batch toxicity test was conducted to identify the toxic constituents in PAX-21 and DNAN was identified as the primary toxicant responsible for inhibiting the activity of perchlorate reducing bacteria. It was hypothesized that pretreatment of PAX-21 by zero-valent iron granules will transform toxic constituents in PAX-21 wastewater to non-toxic products. We observed complete reduction of DNAN to 2,4-diaminoanisole (DAAN) and RDX to formaldehyde in abiotic iron reduction study. After a 3-day acclimation period, perchlorate in iron-treated PAX-21 wastewater was rapidly decreased to an undetectable level in 2 days. This result demonstrated that iron treatment not only removed energetic compounds but also eliminated the toxic constituents that inhibited the subsequent microbial process.

  16. Detoxification of PAX-21 ammunitions wastewater by zero-valent iron for microbial reduction of perchlorate

    Energy Technology Data Exchange (ETDEWEB)

    Ahn, Se Chang; Cha, Daniel K. [Department of Civil and Environmental Engineering, University of Delaware, Newark, DE 19716 (United States); Kim, Byung J. [U.S. Army Engineer Research and Development Center, Champaign, IL 61826-9005 (United States); Oh, Seok-Young, E-mail: [Department of Civil and Environmental Engineering, University of Ulsan, Ulsan 680-749 (Korea, Republic of)


    Highlights: {yields} Ammonium perchlorate, hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and 2,4-dinitroanisole (DNAN) are the major constituents of PAX-21. {yields} DNAN is identified as the primary toxicant responsible for inhibiting the activity of perchlorate reducing bacteria. {yields} Iron treatment not only removes energetic compounds but also eliminates the toxic constituents that inhibit the subsequent microbial process. - Abstract: US Army and the Department of Defense (DoD) facilities generate perchlorate (ClO{sub 4}{sup -}) from munitions manufacturing and demilitarization processes. Ammonium perchlorate is one of the main constituents in Army's new main charge melt-pour energetic, PAX-21. In addition to ammonium perchlorate, hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and 2,4-dinitroanisole (DNAN) are the major constituents of PAX-21. In order to evaluate microbial perchlorate reduction as a practical option for the treatment of perchlorate in PAX-21 wastewater, we conducted biodegradation experiments using glucose as the primary sources of electrons and carbon. Batch experiments showed that negligible perchlorate was removed in microbial reactors containing PAX-21 wastewater while control bottles containing seed bacteria and glucose rapidly and completely removed perchlorate. These results suggested that the constituents in PAX-21 wastewater may be toxic to perchlorate reducing bacteria. A series of batch toxicity test was conducted to identify the toxic constituents in PAX-21 and DNAN was identified as the primary toxicant responsible for inhibiting the activity of perchlorate reducing bacteria. It was hypothesized that pretreatment of PAX-21 by zero-valent iron granules will transform toxic constituents in PAX-21 wastewater to non-toxic products. We observed complete reduction of DNAN to 2,4-diaminoanisole (DAAN) and RDX to formaldehyde in abiotic iron reduction study. After a 3-day acclimation period, perchlorate in iron-treated PAX-21

  17. 溶剂热合成Cu2O微球及其对高氯酸铵热分解的催化作用%Solvo-Thermal Synthesis of Cu2O Micro-Spheres and Their Catalytic Performance for Thermal Decomposition of Ammonium Perchlorate

    Institute of Scientific and Technical Information of China (English)

    罗小林; 韩银凤; 杨德锁; 陈亚芍


    以聚乙烯吡咯烷酮(PVP)为添加剂,利用溶剂热法合成了Cu2O微球.考察了PVP用量以及反应温度对产物形貌的影响,并在反应时间为2.5与4.5 h时分别合成了直径为100-200 nm和1 μm的Cu2O微球.同时,利用差热分析(DTA)技术考察了不同直径的Cu2O微球对高氯酸铵(AP)热分解的催化效果,结果表明:添加2%(w)的直径为100-200 nm和1μm的Cu2O微球使得AP的高温分解温度分别降低了116和118℃,AP在低温阶段的分解量也明显提高.%Cu2O micro-spheres were fabricated by a solvothermal method using poly vinylpyrrolidone (PVP) as an additive. The influences of PVP dosage and reaction temperature on the morphologies of the products were investigated. CuzO micro-spheres with diameters of 100-200 nm and about 1 um were synthesized with reaction time of 2.5 and 4.5 h, respectively. Meanwhile, differential thermal analysis (OTA) was used to determine the catalytic performance of these Cu2O micro-spheres with different diameters for thermal decomposition of ammonium perchlorate (AP). Adding 2% (w) CujO micro-spheres with diameters of 100-200 nm and about 1 um into AP decreased the maximum temperature of AP decomposition by 116 and 118 °C, respectively, and increased the amount of AP decomposed at lower temperature.

  18. 纳米SiO2负载的过渡金属硼化物对AP热分解的催化作用%Catalytic Activity of Nano-silica Supported Transition-metal Borides on the Thermal Decomposition of Ammonium Perchlorate

    Institute of Scientific and Technical Information of China (English)

    李茸; 刘祥萱; 王煊军


    采用化学还原法制备纳米NiB/SiO2、CoB/SiO2、MoB/SiO2催化剂,通过热重-差热分析(TG-DTA)研究了其对AP热分解过程的催化作用.结果表明,负载过渡金属硼化物催化剂对AP分解的催化活性顺序为:CoB/SiO2>NiB/SiO2> MoB/SiO2;加入质量分数5%的CoB/SiO2使AP高温热分解峰温度降低166.2℃;SiO2载体将CoB晶型转化推迟了 110℃左右,改善了催化剂的热稳定性.%The nano-silica supported transition metal catalysts NiB/SiO2 , CoB/SiO2 , MoB/SiO2 were prepared by chemical reduction method. Their catalytic activity on the thermal decomposition of ammonium perchlorate (AP) was studied by TG-DTA. Results show that catalytic activity of nano-silica supported transition metal borides for the thermal decomposition of AP decreases in the order: CoB/SiO2 > NiB/SiO2 >MoB/SiO2. The CoB/SiO2 (mass ration of 5%) catalyst makes the high-temperature thermal decomposition temperature of AP decrease by 166. 2℃. The SiO2 carrier makes the crystal transformation temperature delay about 110℃, revealling the improvement of thermal stability of the catalyst.

  19. Catalytic Effect of NdCoO_3 Nanoparticles on the Thermal Decomposition of Ammonium Perchlorate by DSC/TG-MS%纳米NdCoO_3催化高氯酸铵热分解的DSC/TG-MS研究

    Institute of Scientific and Technical Information of China (English)

    余宗学; 江晓红; 陆路德; 汪信


    Cubic structural perovskite NdCoO_3 nanocrystals were prepared by microemulsion method. The catalytic effect of the NdCoO_3 for thermal decomposition of ammonium perchlorate (AP) was investigated by DSC and TG-MS. The results revealed that the NdCoO_3 nanoparticles had effective catalysis on the thermal decomposition of AP. Adding 2% of NdCoO_3 nanoparticles to AP decreased the temperature of thermal decomposition by 113 ℃ and increased the heat of decomposition from 655 J·g~(-1) to 1 363 J·g~(-1). Gaseous products of thermal decomposition of AP were NH_3, H_2O, O_2, HCl, N_2O, NO, NO_2 and Cl_2. The mechanism of catalytic action was based on the presence of superoxide ion (O_2~-) and oxygenic ion (O~-, O~(2-)) on the surface of NdCoO_3, and the difference of thermal decomposition of AP with 2% of NdCoO_3 and pure AP was mainly caused by the different extent of oxidation of ammonium.%采用微乳液法制备了立方晶系的NdCoO_3纳米晶.利用DSC/TG-MS研究了NdCoO_3对AP热分解的催化作用.结果表明,在NdCoO_3的催化作用下,AP的热分解反应峰值温度下降了113℃,表观分解反应热从655 J·g~(-1)增加到1 363 J·g~(-1),分解的气相产物主要有NH3,H_2O,O_2,HCl,N_2O,NO,NO_2和Cl_2.在金属氧化物表面吸附生成超氧化离子(O_2~-)和氧离子(O~-,O~(2-)),这是加速AP分解反应的主要原因.加入NdCoO_3催化AP热分解,由于对氨的氧化深度不同而导致分解放热量的增加.

  20. Ferrocene Covalently Functionalized Graphene Oxide: Preparation,Characterization and Catalytic Performance for Thermal Decomposition of Ammonium Perchlorate%二茂铁功能化石墨烯氧化物的制备、表征及对高氯酸铵热分解的催化性能

    Institute of Scientific and Technical Information of China (English)

    周磊; 王立; 俞豪杰; 高敬民; 丁文兵; 高浩其


    A new ferrocene modified graphene oxide nano-material (GO-EDA-Fc) was synthesized via a new synthesis route.The GO-EDA-Fc was characterized by Fourier transform infrared spectra,and its morphology was observed under scanning electron microscopy.The graphene oxide was covalently decorated by ferrocene.The catalytic performance of GO-EDA-Fc in the thermal decomposition of ammonium perchlorate(AP) was investigated by thermogravimetric analysis (TGA).The results showed that GO-EDA-Fc exhibited high catalytic activity.When 4wt% of GO-EDA-Fc was added,the peak temperature of the high-temperature decomposition peak of AP had a decrease of 60℃ and the peak of the low-temperature decomposition was shifted to lower as well.The more GO-EDA-Fc was added,the better catalytic performance would be achieved.Notably,the ferrocene functionalized graphenc oxide had shown a synergistic catalytic effect.The mechanism of promote action was also investigated.%本文通过一种新的合成路线合成了二茂铁功能化的氧化石墨烯(GO-EDA-Fc).利用傅里叶变换红外光谱和扫描电子显微镜对其结构和形貌进行了表征.通过热重分析(TGA)研究了其对高氯酸铵(AP)热分解的催化性能,结果表明,氧化石墨烯和二茂铁表现出很好的协同催化效果,对AP热分解具有高的催化活性.催化效果随着GO-EDA-Fc加入量的增加而增强,当加入4wt%的GO-EDA-Fc时,AP的高温分解峰的峰值温度下降了60℃,低温分解峰的峰值也有降低.文中还对催化机制进行了研究.

  1. Catalytic Thermal Decomposition of Ammonium Perchlorate by Cu/Co/Fe Mixed Oxides Derived from Layered Double Hydroxides%Cu/Co/Fe水滑石衍生的复合氧化物催化高氯酸铵热分解的研究

    Institute of Scientific and Technical Information of China (English)

    刘洪博; 黄志勇; 郭冰之; 矫庆泽


    Cu/Co/Fe mixed oxides (Cu/Co/Fe-MOs) were prepared by calcining the precursors of Cu/Co/Fe layered double hydroxides (Cu/Co/Fe-LDHs),and were used as new catalysts for the thermal decomposition of ammonium perchlorate (AP).The catalytic activity was investigated using differential thermal analysis (DTA) and thermal gravimetric analyzer coupled with an online mass spectrometer (TG-MS).The results reveal that Cu/Co/Fe-MOs exhibit CuFe2O4 and (CoFe2)O4 phase with high specific surface area of 70~110 m2·g-1.The Cu/Co/Fe-MOs have homogenous particles with crystallite size of 20~30 nm.The thermal decomposition temperature of AP can be lowered by 139 ℃ with 4wt% of Cu/Co/Fe-MOs calcined at 400 ℃.The improvement in thermal decomposition of AP by Cu/Co/Fe-MOs catalysts is achieved via the superoxide ion (O2-) adsorbed on the surface of Cu/Co/Fe-MOs.%以Cu/Co/Fe水滑石(Cu/Co/Fe-LDHs)为前驱体经过焙烧制备了Cu/Co/Fe复合氧化物(Cu/Co/Fe-MOs).利用DTA和TG-MS研究了Cu/Co/Fe-MOs作为新型催化剂对高氯酸铵热分解的催化性能.结果表明,Cu/Co/Fe-MOs呈现为CuFe2O4和(CoFe2)O4晶相,具有70~110 m2·g-1的比表面积.晶粒大小均匀,尺寸在20~30 nm.添加4wt%的400℃焙烧得到的Cu/Co/Fe-MOs催化剂使高氯酸铵热分解反应的温度降低了139℃.Cu/Co/Fe-MOs是通过吸附在金属氧化物表面的超氧离子(O2-)来加速高氯酸铵热分解的.

  2. An Enzymatic Bioassay for Perchlorate (United States)


    for the hydroponic growth of various fruit and vegetables may contain perchlorate at concentrations as high as 350 (Collette et al., 2003...Such levels could represent a significant global health threat due to the increasing use of hydroponic farming techniques for the production of a...2002). In certain plant species such as tobacco and lettuce the perchlorate accumulated and persisted during processing into the final shelf products

  3. Branched polymeric media: Perchlorate-selective resins from hyperbranched polyethyleneimine

    KAUST Repository

    Chen, Dennis P.


    Perchlorate (ClO4 -) is a persistent contaminant found in drinking groundwater sources in the United States. Ion exchange (IX) with selective and disposable resins based on cross-linked styrene divinylbenzene (STY-DVB) beads is currently the most commonly utilized process for removing low concentrations of ClO4 - (10-100 ppb) from contaminated drinking water sources. However, due to the low exchange capacity of perchlorate-selective STY-DVB resins (∼0.5-0.8 eq/L), the overall cost becomes prohibitive when treating groundwater with higher concentration of ClO4 - (e.g., 100-1000 ppb). In this article, we describe a new perchlorate-selective resin with high exchange capacity. This new resin was prepared by alkylation of branched polyethyleneimine (PEI) beads obtained from an inverse suspension polymerization process. Batch and column studies show that our new PEI resin with mixed hexyl/ethyl quaternary ammonium chloride exchange sites can selectively extract trace amounts of ClO4 - from a makeup groundwater (to below detection limit) in the presence of competing ions. In addition, this resin has a strong-base exchange capacity of 1.4 eq/L, which is 1.75-2.33 times larger than those of commercial perchlorate-selective STY-DVB resins. The overall results of our studies suggest that branched PEI beads provide versatile and promising building blocks for the preparation of perchlorate-selective resins with high exchange capacity. © 2012 American Chemical Society.

  4. Perchlorate Reduction by Yeast for Mars Exploration (United States)

    Sharma, Alaisha


    Martian soil contains high levels (0.6 percentage by mass) of calcium perchlorate (Ca(ClO4)2), which readily dissociates into calcium and the perchlorate ion (ClO4-) in water. Even in trace amounts, perchlorates are toxic to humans and have been implicated in thyroid dysfunction. Devising methods to lessen perchlorate contamination is crucial to minimizing the health risks associated with human exploration and colonization of Mars. We designed a perchlorate reduction pathway, which sequentially reduces perchlorate to chloride (Cl-) and oxygen (O2), for implementation in the yeast Saccharomyces cerevisiae. Using genes obtained from perchlorate reducing bacteria Azospira oryzae and Dechloromonas aromatica, we plan to assemble this pathway directly within S. cerevisiae through recombinational cloning. A perchlorate reduction pathway would enable S. cerevisiae to lower perchlorate levels and produce oxygen, which may be harvested or used directly by S. cerevisiae for aerobic growth and compound synthesis. Moreover, using perchlorate as an external electron acceptor could improve the efficiency of redox-imbalanced production pathways in yeast. Although several perchlorate reducing bacteria have been identified and utilized in water treatment systems on Earth, the widespread use of S. cerevisiae as a synthetic biology platform justifies the development of a perchlorate reducing strain for implementation on Mars.

  5. Rocket Solid Propellant Alternative Based on Ammonium Dinitramide

    Directory of Open Access Journals (Sweden)

    Grigore CICAN


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

  6. Combined effects of exposure to ammonium perchlorate and potassium iodide on apoptosis and oxidative stress in the human thyroid cells%过氯酸铵及碘化钾联合作用对人甲状腺细胞凋亡及氧化应激的影响

    Institute of Scientific and Technical Information of China (English)

    陈红霞; 赵明; 刘琴; 彭开良


    目的:研究过氯酸铵(AP)及碘化钾(KI)联合作用对人甲状腺细胞(nthy-ori3-1)氧化应激及诱导凋亡的影响。方法体外培养 nthy-ori3-1细胞,不同浓度 AP(0、5、10、20、40 mmol/L)及 KI (5 mmol/L)联合染毒后培养24 h,CCK8法检测 nthy-ori3-1细胞的增殖活力,流式细胞仪检测细胞凋亡率及细胞内活性氧(ROS)产生情况,同时测定氧化损伤指标丙二醛(MDA)、过氧化氢酶(CAT)活力。结果 AP 抑制nthy-ori3-1细胞增殖具有明显的剂量依赖性。与对照组比较,各组细胞内 ROS 生成量随着染毒剂量的增加出现降低趋势,除5 mmol/L AP 剂量组外,差异均有统计学意义(P 0.05)。结论 AP 和 KI 联合作用可致 nthy-ori3-1细胞出现氧化应激,且二者之间存在明显的剂量-反应关系,碘在一定程度上可缓解 AP 对甲状腺细胞的氧化应激反应。%Objective To explore the combined effects of ammonium perchlorate (AP)and potassium iodide(KI)on the oxidative stress and apoptosis in Nthy-ori3-1 thyroid cells.Methods The Nthy-ori3-1 cells cultured at 37 ℃,5% CO 2 in vitro,were exposed to different concentrations of AP (10,20,40 mmol/L)and KI(5,25 mmol/L)for 24 h,then the cell proliferation activity was detected by the CCK8 assay,while the apoptosis and intracellular generated reactive oxygen species (ROS)were measured by flow cytometry, simultaneously with the oxidative damage indicators malondialdehyde(MDA)and catalase(CAT)activity being detected.Results The significant dose-dependence relationship was found in the inhibition of Nthy-ori3-1 cell proliferation induced by AP.Compared with the control group,the ROS generation of the cells in each group appeared to decrease with dose increase except for the 5mmol/LAP dose group, and the differences were statistically significant(P 0.05).Conclusions AP might lead to oxidative stress on the Nthy-ori3-1 cell,as well as the significant dose-response relationship between the dose and effect


    Perchlorate has been positively detected only in those materials known to be derived from Chilean caliche, which constitute less than 0.2% of U.S. fertilizer application. The data obtained in the preponderance of investigations suggest that fertilizers do not contribute to envir...

  8. Aripiprazole salts. II. Aripiprazole perchlorate. (United States)

    Freire, Eleonora; Polla, Griselda; Baggio, Ricardo


    The molecular structure of aripiprazole perchlorate (systematic name: 4-(2,3-dichlorophenyl)-1-{4-[(2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)oxy]butyl}piperazin-1-ium perchlorate), C(23)H(28)Cl(2)N(3)O(2)(+)·ClO(4)(-), does not differ substantially from the recently published structure of aripiprazole nitrate [Freire, Polla & Baggio (2012). Acta Cryst. C68, o170-o173]. Both compounds have almost identical bond distances, bond angles and torsion angles. The two different counter-ions occupy equivalent places in the two structures, giving rise to very similar first-order `packing motifs'. However, these elemental arrangements interact with each other in different ways in the two structures, leading to two-dimensional arrays with quite different organizations.

  9. Kinetics for a membrane reactor reducing perchlorate. (United States)

    Padhye, Lokesh; Rainwater, Ken; Jackson, W Andrew; Morse, Audra


    The major objectives of this work were to operate and construct an autohydrogenotrophic reactor and estimate perchlorate degradation kinetics. The results show that autohydrogenotrophic bacteria were cultured in the reactor and capable of removing 3.6 mg/d of perchlorate in the presence of excess hydrogen (99% removal). The reactor was successful in treating the average influent perchlorate concentration of 532 microg/L to the level of 3 microg/L. A first-order relationship was obtained between the concentration of active biomass in the reactor and the hydraulic retention time for the given amount of substrate. During the kinetic loading study, perchlorate removal ranged from 100 to 50%. The kinetic rate of perchlorate degradation observed in this study was 1.62 hr(-1). The significant degradation of perchlorate in these samples indicates the ubiquity of perchlorate-reducing organisms. Additionally, nitrate was simultaneously removed during water treatment (greater than 90% removal). Because of the excess levels of hydrogen, simultaneous removal of nitrate was not believed to significantly affect perchlorate removal. The area of concern was the lack of complete control over biological treatment. The growth of sulfate-reducing organisms in the reactor negatively affected perchlorate removal efficiency. There were no significant effects observed on the dissolved organic carbon and total suspended solids concentration of the effluent, suggesting that the treatment did not produce a large amount of biomass washout.

  10. 纳米结晶体Ni0.5Zn0.5Fe2O4对高氯酸铵热行为及分解反应动力学的影响%Effect of Nanocrystal Ni0.5Zn0.5Fe2O4 on Thermal Behavior and Decomposition Reaction Kinetics of Ammonium Perchlorate

    Institute of Scientific and Technical Information of China (English)

    仪建华; 赵凤起; 胡荣祖; Gurdip Singh


    采用差示扫描量热法(DSC)、热重和微分热重(TG-DTG)及固相原位反应池/快速扫描傅立叶变换红外联用技术(hyphenated in situ thermolysis/RSFTIR)研究了纳米结晶体Ni0.5Zn0.5Fe2O4与高氯酸铵(AP)组成的混合物的热行为和分解反应动力学.结果表明:Ni0.5Zn0.5Fe2O4使得AP的低、高温分解放热峰温分别提前17.44 K和27.74 K,并使得对应的分解热分别增加3.7 J·g-1和193.7 J·g-1.Ni0.5Zn0.5Fe2O4并不影响AP的晶转温度和晶转热.Ni0.5Zn0.5Fe2O4使得AP的TG曲线出现3个阶段,并使得后2个失重阶段的初始和终止温度都有所提前.凝聚相分解产物分析表明Ni0.5Zn0.5Fe2O4加速了凝聚相AP的分解及氨气的释放.含Ni0.5Zn0.5Fe2O4的AP的高温分解反应的动力学参数Ea=238.88 kJ·mol-1,A=1018.59 s-1,动力学方程可表示为dα/dt=1018.99(1-α)[-ln(1-α)]3/5e-2.87.始点温度(Te)和峰顶温度(Tp)计算得出AP的热爆炸临界温度值分别为:574.83 K和595.41 K.分解反应的活化熵(△S≠)、活化焓(△H≠)和活化能(△G≠)分别为:109.61 J·mol-1·K-1、236.49 kJ·mol-1及172.58 kJ·mol-1.%The thermal behavior and non-isothermal decomposition reaction kinetics of the mixture of the nanocrystal Ni0.5Zn0.5Fe2O4 and ammonium perchlorate (AP) were investigated by differential scanning calorimetry(DSC), thermogravimetry and differential thermogravimetry (TG-DTG), and the hyphenated technique of in situ thermolysis cell with rapid-scan Fourier transform infrared spectroscopy (in situ thermolysis/RSFTIR). The results show that Ni0.5Zn0.5Fe2O4 can decrease the low-temperature and the high-temperature exothermic peak temperatures of AP by 17.44 K and 27.74 K, respectively, and increase the decomposition heats of the two exothermic peaks by of AP. Ni0.5Zn0.5Fe2O4 makes AP shown three mass-loss processes, and it can decrease the initial and terminated temperatures of the last two mass-loss stages. The condensed phase decomposition product


    Perchlorate, a component of solid rocket fuels, has emerged as a potential threat to surface water and groundwater at several locations in the U.S. Perchlorate levels up to 16 ug/L were detected in Lake Mead and 5-9 ug/L in the lower Colorado River. The water from the Colorado Ri...


    Previous studies have shown that tobacco plants are tolerant of perchlorate and will accumulate perchlorate in the plant tissues. The objective of this research was to determine the effectiveness of tobacco plants in phytoremediation, a technology that employs plants to degrade,...

  13. The Microbiology of Perchlorate in the Environment (United States)

    Coates, J. D.


    In the last decade perchlorate has been identified as an important groundwater component that poses potential health threat. Although primarily sourced anthropogenically, many recent studies have identified significant natural pools throughout the US and the natural mechanisms of its synthesis remain a mystery. As such, the true perchlorate concentrations naturally present in the environment are still unknown making its regulation problematic. Because of its solubility and non-reactivity the fate and transport of perchlorate in the environment is primarily a function of microbial activity. In the last seven years more than forty specialized perchlorate respiring organisms have been identified and characterized. These dissimilatory perchlorate reducing bacteria (DPRB) are metabolically diverse and environmental populations tend to be dominated by two primary genotypes, the Dechloromonas and the Azospira species. As such, the majority of our understanding of this metabolism is based on these organisms. These organisms are readily found in soil and sedimentary environments and often associate with the rhizosphere. Recent research has demonstrated an accumulation of these organisms along plant roots suggesting their catabolism of root exudates and molecular studies has demonstrated their existence as endophytic infections of the stem and leaves of actively growing Brachypodium grass plants although their exact role under these conditions is unknown. These microorganisms are generally not nutritionally fastidious and vitamin supplementation is unnecessary for growth although molybdenum is a required trace element for perchlorate reduction. The Dechloromonas and Azospira species generally grow optimally at pH values near neutrality in freshwater environments. Even so, recent field studies have shown that related deep-branching members of these genera often predominate in sites of adverse pH or salinity with some species being capable of growth and perchlorate respiration

  14. Insensitive Ammonium Nitrate. (United States)

    is reduced by replacing the ammonium nitrate with a solid solution of potassium nitrate in form III ammonium nitrate wherein the potassium nitrate...constitutes from more than zero to less than 50 weight percent of the solid solution . (Author)


    The most comprehensive survey of fertilizers and other raw materials for perchlorate to date has been conducted to determine whether these could be significant contributors to environmental perchlorate contamination. Although the data span a large range of commercial products, th...

  16. Elevated ammonium levels

    DEFF Research Database (Denmark)

    Søgaard, Rikke; Novak, Ivana; MacAulay, Nanna


    ]glutamate uptake and glutamate transport currents but had no effect on EAAT2. The maximal EAAT3-mediated glutamate transport current was increased but the apparent affinities for glutamate and Na(+) were unaltered. Ammonium did not affect EAAT3-mediated transient currents, indicating that EAAT3 surface expression...... was not enhanced. The ammonium-induced stimulation of EAAT3 increased with increasing extracellular pH, suggesting that the gaseous form NH(3) mediates the effect. An ammonium-induced intracellular alkalinization was excluded as the cause of the enhanced EAAT3 activity because 1) ammonium acidified the oocyte...... cytoplasm, 2) intracellular pH buffering with MOPS did not reduce the stimulation, and 3) ammonium enhanced pH-independent cysteine transport. Our data suggest that the ammonium-elicited uptake stimulation is not caused by intracellular alkalinization or changes in the concentrations of cotransported ions...

  17. Ammonium nitrate: a promising rocket propellant oxidizer (United States)

    Oommen; Jain


    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.

  18. Kinetics of chlorite dismutase in a perchlorate degrading reactor sludge. (United States)

    Nadaraja, Anupama Vijaya; Veetil, Prajeesh Gangadharan Puthiya; Vidyadharan, Athira; Bhaskaran, Krishnakumar


    Kinetics of chlorite dismutase (CD), the terminal enzyme involved in the perchlorate (ClO4(-)) reduction pathway, in a ClO4(-)-degrading bioreactor are reported in this study. Enzyme activity was determined from dissolved oxygen released during disproportionation of chlorite (ClO2(-)). CD activity was in the range 29.8-36.4 U/mg dry weight sludge, and kinetic constants Vmax and K(m) of the enzyme were 37.83 U/mg dry weight and 0.28 mM, respectively. Among reactor operational conditions, enzyme activity was observed at pH 4.0-9.0, with an optimum at pH 6.0. Redox potential in the range -50 to +120mV and NaCl up to 3.5 g/L had no significant effect on CD activity. However, co-occurring pollutants such as ammonium at 10 ppm, nitrite at 50 ppm and EDTA at 100 microM reduced CD activity substantially. The present study highlights ideal bioreactor conditions to avoid ClO2(-) toxicity, while indicating the buffering potential of a mixed microbial system against inhibiting factors to maintain stable CD activity in bioreactors.

  19. Atmospheric origins of perchlorate on Mars and in the Atacama (United States)

    Catling, D. C.; Claire, M. W.; Zahnle, K. J.; Quinn, R. C.; Clark, B. C.; Hecht, M. H.; Kounaves, S.


    Isotopic studies indicate that natural perchlorate is produced on Earth in arid environments by the oxidation of chlorine species through pathways involving ozone or its photochemical products. With this analogy, we propose that the arid environment on Mars may have given rise to perchlorate through the action of atmospheric oxidants. A variety of hypothetical pathways can be proposed including photochemical reactions, electrostatic discharge, and gas-solid reactions. Because perchlorate-rich deposits in the Atacama desert are closest in abundance to perchlorate measured at NASA's Phoenix Lander site, we made a preliminary study of the means to produce Atacama perchlorate to help shed light on the origin of Martian perchlorate. We investigated gas phase pathways using a 1-D photochemical model. We found that perchlorate can be produced in sufficient quantities to explain the abundance of perchlorate in the Atacama from a proposed gas phase oxidation of chlorine volatiles to perchloric acid. The feasibility of gas phase production for the Atacama provides justification for future investigations of gas phase photochemistry as a possible source for Martian perchlorate.

  20. Anatase-brookite mixed phase nano TiO2 catalyzed homolytic decomposition of ammonium nitrate. (United States)

    Vargeese, Anuj A; Muralidharan, Krishnamurthi


    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.


    Previous studies have shown that tobacco plants are tolerant of perchlorate and will accumulate perchlorate in plant tissues. This research determined the uptake, translocation, and accumulation of perchlorate in tobacco plants. Three hydroponics growth studies were completed u...

  2. The NAS perchlorate review: questions remain about the perchlorate RfD. (United States)

    Ginsberg, Gary; Rice, Deborah


    Human exposure to perchlorate is commonplace because it is a contaminant of drinking water, certain foods, and breast milk. The U.S. Environmental Protection Agency (EPA) conducted a perchlorate risk assessment in 2002 that yielded a reference dose (RfD) based on both the animal and human toxicology data. This assessment has been superceded by a recent National Academy of Science (NAS) review that derived a perchlorate RfD that is 20-fold greater (less stringent) than that derived by the U.S. EPA in 2002. The NAS-derived RfD was put on the U.S. EPA's Integrated Risk Information System (IRIS) database very quickly and with no further public review. In this commentary we raise concerns about the NAS approach to RfD development in three areas of toxicity assessment: the dose that the NAS described as a no observable adverse-effect level is actually associated with perchlorate-induced effects; consideration of uncertainties was insufficient; and the NAS considered the inhibition of iodine uptake to be a nonadverse effect. We conclude that risk assessors should carefully evaluate whether the IRIS RfD is the most appropriate value for assessing perchlorate risk.

  3. Crystal structure of tin(II perchlorate trihydrate

    Directory of Open Access Journals (Sweden)

    Erik Hennings


    Full Text Available The title compound, [Sn(H2O3](ClO42, was synthesized by the redox reaction of copper(II perchlorate hexahydrate and metallic tin in perchloric acid. Both the trigonal–pyramidal [Sn(H2O3]2+ cations and tetrahedral perchlorate anions lie on crystallographic threefold axes. In the crystal, the cations are linked to the anions by O—H...O hydrogen bonds, generating (001 sheets.

  4. Atmospheric Production of Perchlorate on Earth and Mars (United States)

    Claire, M.; Catling, D. C.; Zahnle, K. J.


    Natural production and preservation of perchlorate on Earth occurs only in arid environments. Isotopic evidence suggests a strong role for atmospheric oxidation of chlorine species via pathways including ozone or its photochemical derivatives. As the Martian atmosphere is both oxidizing and drier than the driest places on Earth, we propose an atmospheric origin for the Martian perchlorates measured by NASA's Phoenix Lander. A variety of hypothetical formation pathways can be proposed including atmospheric photochemical reactions, electrostatic discharge, and gas-solid reactions. Here, we investigate gas phase formation pathways using a 1-D photochemical model (Catling et al. 2009, accepted by JGR). Because perchlorate-rich deposits in the Atacama desert are closest in abundance to perchlorate measured at NASA's Phoenix Lander site, we start with a study of the means to produce Atacama perchlorate. We found that perchlorate can be produced in sufficient quantities to explain the abundance of perchlorate in the Atacama from a proposed gas phase oxidation of chlorine volatiles to perchloric acid. These results are sensitive to estimated reaction rates for ClO3 species. The feasibility of gas phase production for the Atacama provides justification for further investigations of gas phase photochemistry as a possible source for Martian perchlorate. In addition to the Atacama results, we will present a preliminary study incorporating chlorine chemistry into an existing Martian photochemical model (Zahnle et al. JGR 2008).

  5. Evidence for the distribution of perchlorates on Mars (United States)

    Clark, Benton C.; Kounaves, Samuel P.


    Various Mars missions have detected Cl atoms, chlorides and perchlorates in martian surface materials. The global soils, in particular, always contain significant levels of observable Cl. Direct evidence points to this Cl being in the form of both chlorides and perchlorates, and possibly also chlorates and other oxychlorines. The most widespread measurements have been of Cl atoms, and cannot discern the chemical form. However, from separate evidence of perchlorate obtained at high latitudes (Phoenix lander) and low latitudes (Curiosity rover), it is likely that perchlorates are widespread, albeit in varying proportions relative to the total amount of ubiquitous Cl.

  6. Perchlorate Remediation Using New Nanoscale Polymer Technology (United States)


    conditions to give a total of 101 g product. Reduce Amount of Reagents The propargyl tosylate initiated PEOX was analyzed for acetylene content. There...the copper(I) catalyzed reaction between azide functional groups (-N3) and propargyl or acetylenic functional groups (-C≡C-), has become a major...available at an affordable price . This potential perchlorate binding site was reacted with PEOX DP= 100 as a model compound in methanol. 1H-NMR and SEC

  7. Microbial (per)chlorate reduction in hot subsurface environments

    NARCIS (Netherlands)

    Liebensteiner, M.



    The microbial reduction of chlorate and perchlorate has been known for long as a respiratory process of mesophilic bacteria that thrive in diverse environments such as soils, marine and freshwater sediments. Chlorate and perchlorate are found in nature deriving from anthropogenic and

  8. Validation of Chlorine and Oxygen Isotope Ratio Analysis to Differentiate Perchlorate Sources and to Document Perchlorate Biodegradation (United States)


    67 ii 4.5 SUMMARY OF LONG ISLAND PERCHLORATE SOURCE STUDY .......................... 67 5.0 SUMMARY AND CONCLUSIONS...Chilean nitrate fertilizer. 4.5 SUMMARY OF LONG ISLAND PERCHLORATE SOURCE STUDY The stable isotope results (δ37Cl, δ18O, and Δ17O) for ClO4- and key

  9. The use of bis (-2-ethylhexyl) phosphoric acid for the extraction of zinc from concentrated ammonium chloride solutions

    Energy Technology Data Exchange (ETDEWEB)

    Amer, S.; Luis, A.; Cuadra, A. de la; Caravaca, C.


    The extraction of zinc from concentrated ammonium chloride solutions by means of the bis(-2-ethylhexyl) phosphoric acid is studied. Mass balances and chemical equilibria relating the different chemical species in both phases are presented in order to establish a model describing the behaviour of the different species. Good agreement between experimental data and theoretical curves is obtained. A comparison of the zinc extraction from a strong complexing medium as that of concentrated ammonium chloride solutions with an uncomplexing zinc perchlorate solution is made, in order to see the influence of the complexing effect of the aqueous phase on zinc extraction. (Author) 36 p.

  10. Perchlorates as Powerful Catalysts in Many Important Organic Transformations

    Institute of Scientific and Technical Information of China (English)

    G. Bartoli; L. Sambri; M. Locatelli


    @@ 1Introduction For long times, metallic perchlorates have been considered dangerous compounds[1] in that they function as explosives and as incontrollable oxidizers. Therefore, the fear of the great hazard connected with their manufacture and uses had prevented an extensive use both in research laboratories and in industrial processes[2].However, recently it has been cleared that this bad reputation is due to the mistaken association of metallic perchlorates with the oxidizing potential of perchloric acid and the pyrotechnic performances of NH4ClO4.

  11. AP的安全制备%Safe Preparations of Fine Ammonium Perchlorate Particles

    Institute of Scientific and Technical Information of China (English)

    Makoto Kohga


    Fine AP particles are required to manufacture the AP-based composite propellants with a wide burning rate range for various applications,especially high burning rate propellants. However,it is difficult to prepare a fine AP safely. Some safe methods for preparing the fine AP particles are reported such as the spray-dry method and freeze-dry method. It is shown that the crystal habit modified AP particle is an effective oxidizer to enhance the burning rate.

  12. Environmental Health Assessment for Work Unit RM 08-03, Ammonium Perchlorate Alternatives (Ionic Liquids) (United States)


    identified and retrieved using PubMed®, the OVid® Technologies Journals, and the EBSCOhost ® Research Database . (TOXNET®, ChemIDPlusLite®, ChemIDPlus®, HSDB...information for chemical substances. The CASRN is readily used as a keyword for searching online databases and is often cross-referenced with both...individual databases including ChemlDPlus (CIDPL) Lite® and ChemlDPlus® Advanced (Le., chemical and registration numbers, and chemical


    Anaerobic biological processes effectively reduce perchlorate to chloride. However, the effluent can be biologically unstable, high in particulates and high in disinfection by-product precursor compounds. Such an effluent would be unsuitable for transmission into a drinking water...

  14. High pressure studies of potassium perchlorate (United States)

    Pravica, Michael; Wang, Yonggang; Sneed, Daniel; Reiser, Sharissa; White, Melanie


    Two experiments are reported on KClO4 at extreme conditions. A static high pressure Raman study was first conducted to 18.9 GPa. Evidence for at least two new phases was observed: one between 2.4 and 7.7 GPa (possibly sluggish), and the second near 11.7 GPa. Then, the X-ray induced decomposition rate of potassium perchlorate (KClO4 → hν KCl + 2O2) was studied up to 15.2 GPa. The time-dependent growth of KCl and O2 was monitored. The decomposition rate slowed at higher pressures. We present the first direct evidence for O2 crystallization at higher pressures, demonstrating that O2 molecules aggregate at high pressure.

  15. Elimination of Perchlorate Oxidizers from Yellow Pyrotechnic Flare Compositions (United States)


    Conference Presentation 3. DATES COVERED (From - To) 2002-2015 4. TITLE AND SUBTITLE Elimination of Perchlorate Oxidizers from Yellow Pyrotechnic...increasing government regulations to limit ground water contamination. A perchlorate-free yellow flare composition for future implementation into the Mk 144...utilizes sodium nitrate , barium nitrate , and polyvinyl chloride as alternative oxidizers to produce Na emission lines in the orange region of the spectrum

  16. Novel Electrochemical Process for Treatment of Perchlorate in Waste Water (United States)


    technology combines ion exchange and electrochemistry to provide a selective and reversible method for removing target species from wastewater. In...nanotube nanocomposite for removing perchlorate from drinking water and wastewater. The ESIX technology combines ion exchange and electrochemistry to...potential for perchlorate occurrence in drinking water and food supplies is a human health concern because it can interfere with iodide uptake by the

  17. Perchlorate Reductase Is Distinguished by Active Site Aromatic Gate Residues. (United States)

    Youngblut, Matthew D; Tsai, Chi-Lin; Clark, Iain C; Carlson, Hans K; Maglaqui, Adrian P; Gau-Pan, Phonchien S; Redford, Steven A; Wong, Alan; Tainer, John A; Coates, John D


    Perchlorate is an important ion on both Earth and Mars. Perchlorate reductase (PcrAB), a specialized member of the dimethylsulfoxide reductase superfamily, catalyzes the first step of microbial perchlorate respiration, but little is known about the biochemistry, specificity, structure, and mechanism of PcrAB. Here we characterize the biophysics and phylogeny of this enzyme and report the 1.86-Å resolution PcrAB complex crystal structure. Biochemical analysis revealed a relatively high perchlorate affinity (Km = 6 μm) and a characteristic substrate inhibition compared with the highly similar respiratory nitrate reductase NarGHI, which has a relatively much lower affinity for perchlorate (Km = 1.1 mm) and no substrate inhibition. Structural analysis of oxidized and reduced PcrAB with and without the substrate analog SeO3 (2-) bound to the active site identified key residues in the positively charged and funnel-shaped substrate access tunnel that gated substrate entrance and product release while trapping transiently produced chlorate. The structures suggest gating was associated with shifts of a Phe residue between open and closed conformations plus an Asp residue carboxylate shift between monodentate and bidentate coordination to the active site molybdenum atom. Taken together, structural and mutational analyses of gate residues suggest key roles of these gate residues for substrate entrance and product release. Our combined results provide the first detailed structural insight into the mechanism of biological perchlorate reduction, a critical component of the chlorine redox cycle on Earth.

  18. Determination of Perchlorate in Bottled Water from Italy

    Directory of Open Access Journals (Sweden)

    Patrizia Iannece


    Full Text Available Perchlorate is regarded as an emerging persistent inorganic contaminant. It is widely known that perchlorate is an endocrine disruptor as it competitively inhibits iodide transport in the thyroid gland. As drinking water is the major source of human exposure to perchlorate, its occurrence in commercially available bottled waters purchased in different regions of Italy was investigated. Perchlorate was measured using the rapid, sensitive, and selective LC-ESI-MS/MS (liquid chromatography-electrospray tandem mass spectrometry method by multiple reaction monitoring (MRM of the transition 98.8→82.8, which corresponds to the loss of one oxygen atom in the perchlorate ion (ClO4−→ClO3−. The chlorine isotope ratio (35Cl/37Cl was used as a confirmation tool. The limit of quantification (LOQ for this method was 5 ng/L, and the recovery ranged from 94% to 108%. Perchlorate was detected in 44 of the 62 drinking waters tested, with concentrations ranging from <5 to 75 ng/L. These values are similar in magnitude to those reported in drinking water from the USA and do not pose an immediate health concern.

  19. Thermal and Evolved Gas Analysis of Magnesium Perchlorate: Implications for Perchlorates in Soils at the Mars Phoenix Landing Site (United States)

    Ming, Douglas W.; Morris, R.V.; Lauer, H. V.; Sutter, B.; Golden, D.C.; Boynton, W.V.


    Perchlorate salts were discovered in the soils around the Phoenix landing site on the northern plains of Mars [1]. Perchlorate was detected by an ion selective electrode that is part of the MECA Wet Chemistry Laboratory (WCL). The discovery of a mass 32 fragment (likely 02) by the Thermal and Evolved-Gas Analyzer (TEGA) provided additional confirmation of a strong oxidizer in the soils around the landing site. The purpose of this paper is to evaluate the thermal and evolved gas behavior of perchlorate salts using TEGA-like laboratory testbed instruments. TEGA ovens were fabricated from high purity Ni. Hence, an additional objective of this paper is to determine the effects that Ni might have on the evolved gas behavior of perchlorate salts.

  20. Perchlorate in The Great Lakes: Distribution, Isotopic Composition and Origin (United States)

    Poghosyan, A.; Sturchio, N. C.; Jackson, W. A.; Guan, Y.; Eiler, J. M.; Hatzinger, P. B.


    Concentrations, stable chlorine and oxygen isotopic compositions, and 36Cl abundances of perchlorate were investigated in the five Laurentian Great Lakes. Samples were collected during monitoring cruises in 2007 and 2008 of the U.S. EPA's RV Lake Guardian and in 2010 at the water supply intake of Marquette, MI on the southern shore of Lake Superior. Concentrations of perchlorate were measured by IC/MS/MS at 24 locations, including one or two depth profiles in each lake. Mean concentrations (μg/L) are: Superior, 0.06 × 0.01; Michigan, 0.10 × 0.01; Huron, 0.11 × 0.01; Erie, 0.08 × 0.01, and Ontario, 0.09 × 0.01. Concentration vs. depth is nearly constant in each lake, indicating well-mixed conditions. Perchlorate was extracted from near-surface water by passing 15,000 to 80,000 L of water through 1-L cartridges containing Purolite A530E bifunctional anion-exchange resin. In the laboratory, perchlorate was eluted from the resin, purified, and precipitated as a >99% pure crystalline phase. Milligram amounts were recovered from each lake. Chlorine and oxygen isotopic analyses were performed at Caltech using the Cameca 7f-GEO SIMS instrument, following validation of the SIMS method with analyses of USGS-37 and USGS-38 isotopic reference materials. Results indicate a relatively narrow range in δ37Cl values (+2.9 to +3.9 ‰) and a wider range in δ18O values (-4.0 to +4.1 ‰), with a general geographic trend of increasing δ18O from west to east. Oxygen-17 was measured at UIC using dual-inlet IRMS of O2 produced by decomposition of KClO4. Great Lakes perchlorate has mass-independent oxygen isotopic variations with positive Δ17O values (+1.6 ‰ to +2.7 ‰) divided into two distinct groups: Lake Superior (+2.7 ‰) and the other four lakes (~ +1.7 ‰). The isotopic data indicate that perchlorate is dominantly of natural origin, having stable isotopic compositions resembling those of perchlorate from pre-industrial groundwaters in the western USA. The 36Cl

  1. Rate and extent of aqueous perchlorate removal by iron surfaces. (United States)

    Moore, Angela M; De Leon, Corinne H; Young, Thomas M


    The rate and extent of perchlorate reduction on several types of iron metal was studied in batch and column reactors. Mass balances performed on the batch experiments indicate that perchlorate is initially sorbed to the iron surface, followed by a reduction to chloride. Perchlorate removal was proportional to the iron dosage in the batch reactors, with up to 66% removal in 336 h in the highest dosage system (1.25 g mL(-1)). Surface-normalized reaction rates among three commercial sources of iron filings were similar for acid-washed samples. The most significant perchlorate removal occurred in solutions with slightly acidic or near-neutral initial pH values. Surface mediation of the reaction is supported by the absence of reduction in batch experiments with soluble Fe2+ and also by the similarity in specific reaction rate constants (kSA) determined for three different iron types. Elevated soluble chloride concentrations significantly inhibited perchlorate reduction, and lower removal rates were observed for iron samples with higher amounts of background chloride contamination. Perchlorate reduction was not observed on electrolytic sources of iron or on a mixed-phase oxide (Fe3O4), suggesting that the reactive iron phase is neither pure zerovalent iron nor the mixed oxide alone. A mixed valence iron hydr(oxide) coating or a sorbed Fe2+ surface complex represent the most likely sites for the reaction. The observed reaction rates are too slow for immediate use in remediation system design, but the findings may provide a basis for future development of cost-effective abiotic perchlorate removal techniques.

  2. Perchlorate, iodine supplements, iodized salt and breast milk iodine content

    Energy Technology Data Exchange (ETDEWEB)

    Kirk, Andrea B. [Department of Epidemiology, School of Public Health, University of North Texas Health Sciences Center, 3500 Camp Bowie Blvd., Fort Worth, TX 76107 (United States); Kroll, Martina; Dyke, Jason V.; Ohira, Shin-Ichi; Dias, Rukshan A.; Dasgupta, Purnendu K. [Department of Chemistry and Biochemistry, 700 Planetarium Place, University of Texas at Arlington, Arlington, TX 76019 (United States)


    This study was undertaken to determine if increasing maternal iodine intake through single dose tablets will decrease breast milk concentrations of the iodine-uptake inhibitor, perchlorate, through competitive inhibition. We also sought to determine if the timing of supplementation influences the fraction of iodine excreted in milk versus urine and to compare the effectiveness of iodized salt as a means of providing iodine to breastfed infants. Thirteen women who did not use supplements, seven of whom used iodized salt and six of whom used non-iodized salt, submitted four milk samples and a 24-h urine collection daily for three days. Women repeated the sampling protocol for three more days during which {approx} 150 {mu}g of iodine were taken in the evening and again for three days with morning supplementation. Samples were analyzed using isotope-dilution inductively-coupled plasma-mass spectrometry for iodine and isotope-dilution ion chromatography-tandem mass spectrometry for perchlorate. No statistically significant differences were observed in milk iodine or perchlorate concentrations during the two treatment periods. Estimated perchlorate intake was above the U.S. National Academy of Sciences suggested reference dose for most infants. Single daily dose iodine supplementation was not effective in decreasing milk perchlorate concentrations. Users of iodized salt had significantly higher iodine levels in milk than non-users. Iodized salt may be a more effective means of iodine supplementation than tablets. - Highlights: Black-Right-Pointing-Pointer Estimated infant exposures to perchlorate were, on a {mu}g/kg basis, {approx} 5 Multiplication-Sign higher than those of mothers. Black-Right-Pointing-Pointer Daily supplements are less effective than iodized salt in providing iodine to lactating women. Black-Right-Pointing-Pointer Low iodine and high perchlorate in milk may place infants at risk of iodine deficiency.

  3. Evaluation of an Innovative Technology for Treatment of Water Contaminated with Perchlorate and Organic Compounds (United States)


    Environment: Emerging Contaminants /MERIT: Emerging Contaminants (EC): EC Action List: Perchlorate. Retrieved 2 July 2008, from: https...Trichloroethylene, Perchlorate, and Other Emerging Contaminants . Testimony Before the Subcommittee on Readiness, Committee on Armed Services, House of

  4. 高氯酸盐的环境毒理学效应及其机制的研究进展%Environmental toxicological effect and mechanism of perchlorate

    Institute of Scientific and Technical Information of China (English)

    吴春笃; 李顺; 许小红; 张波


    Perchlorate is a persistent toxic contaminant in the environment and the environmental problems caused have drawn the extensive attention of human beings. The perchlorate rarely exists in natural environment and mainly exists in the soil, furthermore, the atmosphere also produces a certain amount of perchlorate in some conditions. The pollution is mainly caused by the mass production and use of ammonium perchlorate and potassium perchlorate. Perchlorate is quite soluble,it can be rapidly transported and diffused in aqueous systems and achieve enrichment in plants and animals, then enters into human body through ingestion behavior. By competing with the sodium-iodide symporter (NIS) for transporting iodide into thyroid, perchlorate inhibits iodide uptake,influences the thyroid and pituitary hormone level and then inhibits the normal metabolism and growth of organisms. Based on the perchlorate toxicology data of potential adverse effects on thyroid function,growth, development,reproduction and neurodevelopment, this paper reviewed the perchlorate toxicity mechanism and the future research prospect was presented.%高氯酸盐是一种具有持久性的有毒污染物质,其环境污染问题引起了人类的广泛关注.天然环境中的高氯酸盐比例很少,主要存在于土壤中;此外,在某些环境条件下,大气中也能产生一定量的高氯酸盐;其人为污染主要来源于大量生产和使用的高氯酸铵和高氯酸钾.高氯酸盐易溶于水,可以在水环境中快速迁移扩散,在动植物体内富集并通过人类摄食作用进入人体.高氯酸根能够竞争性利用钠/碘转运体(NIS),抑制甲状腺吸收碘离子,进而影响甲状腺和脑垂体的激素水平,阻碍生物体正常的新陈代谢和生长发育.笔者基于高氯酸盐对甲状腺、生长发育、生殖行为及神经系统等潜在危害的毒理学研究,综述了高氯酸盐对生物体的毒性作用机制,并对其研究前景进行了展望.

  5. Oxygen and Chlorine Isotopic Fractionation During Microbial Reduction of Perchlorate (United States)

    Beloso, A. D.; Sturchio, N. C.; Böhlke, J. K.; Streger, S. H.; Heraty, L. J.; Hatzinger, P. B.


    Perchlorate is a widespread environmental contaminant that has both anthropogenic and natural sources. Stable isotope ratios of O and Cl in perchlorate have been used recently to distinguish perchlorate of different origins. Isotopic ratios may also be useful for identifying the occurrence and extent of biodegradation of perchlorate in natural environments, information that is critical for assessing natural attenuation of this contaminant. For this approach to be useful, however, the extent of isotopic fractionation of both Cl and O by bacteria must be determined, and the influence of environmental variables on this process must be defined. During this laboratory study, the O and Cl isotope ratios of perchlorate were monitored as a function of degradation by two separate bacterial species (Azospira suillum JPLRND and Dechlorospirillum sp. FBR2) at both 10 °C and 22 °C with acetate as the electron donor. Perchlorate was completely degraded by both strains within 280 hr at 22 °C and 615 hr at 10 °C. Measured values of isotopic fractionation factors were ɛ18O = -36.6 to -29.0 ‰ and ɛ37Cl = -14.5 to - 11.5 ‰, and these showed no apparent systematic variation with either temperature or bacterial strain. One experiment using 18O-enriched water (δ18O = 200‰) gave results indistinguishable from those observed in isotopically normal water, indicating little or no isotopic exchange between perchlorate and water during biodegradation. The fractionation factor ratio ɛ18O/ɛ37Cl was nearly invariant in all experiments at 2.50 ± 0.04. These data indicate that isotopic analysis will be useful for documenting perchlorate biodegradation in soils and groundwater. The establishment of a microbial fractionation factor ratio (ɛ18O/ɛ37Cl) also has significance for forensic studies, as these data indicate that fractionation via biodegradation will not cause the reported mass-dependent Cl and O isotopic signatures of synthetic and natural perchlorate to overlap.

  6. Perchlorates are compatible with life on Earth: Why not Mars? (United States)

    Kolb, Vera M.; Hoover, Richard


    Perchlorates have been found on the surface of Mars. Since they are strongly oxidizing, it is important to discuss how this fact is reflected both on the existence of organic compounds on the surface of Mars and possibly life. We have previously reported that perchlorates, although strongly oxidizing, do not destroy some amino acids, such as glycine and alanine, among others, and also spare other classes of organic compounds. Others have found that perchlorates are utilized by bacteria and Archaea as energy sources. Particularly important are the findings about Archaea, since they show a combination of a biotic and abiotic processing of perchlorates, which implies ancient origins of these pathways, which may have been typical on prebiotic Earth. There are also numerous reports of the presence of organohalogen compounds on Earth which are made by natural sources or living organisms. Such compounds may be simple, such as chloromethane, or very complicated. They are utilized or produced by living organisms on Earth. Significantly, some such compounds are extremely stable to high temperatures, over 400oC, which should be taken into account for the chemical analyses on Mars. Finally, organohalogen compounds have been also detected on the meteorites. This combined evidence indicates that eventual finding of the organohalogen compounds on Mars is expected, and that the presence of the strongly oxidizing perchlorates does not rule out life on Mars.

  7. Ammonium diphosphitoindate(III

    Directory of Open Access Journals (Sweden)

    Farida Hamchaoui


    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.

  8. Waterproofing Materials for Ammonium Nitrate

    Directory of Open Access Journals (Sweden)

    R.S. Damse


    Full Text Available This study explores the possibility of overcoming the problem of hygroscopicity of ammonium nitrate by coating the particles with selected waterproofing materials. Gravimetric analysis ofthe samples of ammonium nitrate coated with eight different waterproofing materials, vis-a-vis, uncoated ammonium nitrate, were conducted at different relative humidity and exposuretime. The results indicate that mineral jelly is the promising waterproofing material for ammonium nitrate among the materials tested, viz, calcium stearate, dioctyl phthalate, kaoline, diethylphthalate, dinitrotoluene, shelac varnish, and beeswax. Attempts were made to confirm the waterproofing ability of mineral jelly to ammonium nitrate using differential thermal analysisand x-ray diffraction patterns as an experimental tool. Suitability of mineral jelly as an additive for the gun propellant was also assessed on the basis of theoretical calculations using THERMprogram.

  9. A bioinspired iron catalyst for nitrate and perchlorate reduction. (United States)

    Ford, Courtney L; Park, Yun Ji; Matson, Ellen M; Gordon, Zachary; Fout, Alison R


    Nitrate and perchlorate have considerable use in technology, synthetic materials, and agriculture; as a result, they have become pervasive water pollutants. Industrial strategies to chemically reduce these oxyanions often require the use of harsh conditions, but microorganisms can efficiently reduce them enzymatically. We developed an iron catalyst inspired by the active sites of nitrate reductase and (per)chlorate reductase enzymes. The catalyst features a secondary coordination sphere that aids in oxyanion deoxygenation. Upon reduction of the oxyanions, an iron(III)-oxo is formed, which in the presence of protons and electrons regenerates the catalyst and releases water.

  10. Preliminary assessment of perchlorate in ecological receptors at the Longhorn Army Ammunition Plant (LHAAP), Karnack, Texas. (United States)

    Smith, P N; Theodorakis, C W; Anderson, T A; Kendall, R J


    There have been increasing human health and ecological concerns about ionic perchlorate (ClO4-) since it was detected in drinking water sources in 1997. Perchlorate is known to affect thyroid function, causing subsequent hormone disruption and potential perturbations of metabolic activities. According to current estimates, perchlorate is found in the surface of groundwater of 14 states, including Texas. Longhorn Army Ammunition Plant, located in east central Texas, was a facility historically associated with perchlorate-containing propellants and rocket motors. Subsequently, perchlorate contamination in ground and surface waters at the facility has been reported. Soil, sediment, water, vegetation, and animal tissue samples were collected from several locations within the plant for a preliminary site assessment of perchlorate contamination. Perchlorate concentrations ranged from 555-5,557,000 ppb in vegetation, 811-2038 ppb in aquatic insects, below detection limits (ND) to 207 ppb in fish, ND-580 ppb in frogs, and ND-2328 ppb in mammals. Consistent with our hypothesis, aquatic organisms inhabiting perchlorate-contaminated surface water bodies contained detectable concentrations of perchlorate. Additionally, terrestrial organisms were exposed through pathways not necessarily related to contaminated surface waters. Therefore, these data demonstrate that aquatic and terrestrial species are exposed to perchlorate in the environment. To our knowledge, this represents the first incidence of perchlorate exposure among wild animals reported in the scientific literature.

  11. An upper-bound assessment of the benefits of reducing perchlorate in drinking water. (United States)

    Lutter, Randall


    The Environmental Protection Agency plans to issue new federal regulations to limit drinking water concentrations of perchlorate, which occurs naturally and results from the combustion of rocket fuel. This article presents an upper-bound estimate of the potential benefits of alternative maximum contaminant levels for perchlorate in drinking water. The results suggest that the economic benefits of reducing perchlorate concentrations in drinking water are likely to be low, i.e., under $2.9 million per year nationally, for several reasons. First, the prevalence of detectable perchlorate in public drinking water systems is low. Second, the population especially sensitive to effects of perchlorate, pregnant women who are moderately iodide deficient, represents a minority of all pregnant women. Third, and perhaps most importantly, reducing exposure to perchlorate in drinking water is a relatively ineffective way of increasing iodide uptake, a crucial step linking perchlorate to health effects of concern.

  12. Simultaneous detection of perchlorate and bromate using rapid high-performance ion exchange chromatography-tandem mass spectrometry and perchlorate removal in drinking water. (United States)

    West, Danielle M; Mu, Ruipu; Gamagedara, Sanjeewa; Ma, Yinfa; Adams, Craig; Eichholz, Todd; Burken, Joel G; Shi, Honglan


    Perchlorate and bromate occurrence in drinking water causes health concerns due to their effects on thyroid function and carcinogenicity, respectively. The purpose of this study was threefold: (1) to advance a sensitive method for simultaneous rapid detection of perchlorate and bromate in drinking water system, (2) to systematically study the occurrence of these two contaminants in Missouri drinking water treatment systems, and (3) to examine effective sorbents for minimizing perchlorate in drinking water. A rapid high-performance ion exchange chromatography-tandem mass spectrometry (HPIC-MS/MS) method was advanced for simultaneous detection of perchlorate and bromate in drinking water. The HPIC-MS/MS method was rapid, required no preconcentration of the water samples, and had detection limits for perchlorate and bromate of 0.04 and 0.01 μg/L, respectively. The method was applied to determine perchlorate and bromate concentrations in total of 23 selected Missouri drinking water treatment systems during differing seasons. The water systems selected include different source waters: groundwater, lake water, river water, and groundwater influenced by surface water. The concentrations of perchlorate and bromate were lower than or near to method detection limits in most of the drinking water samples monitored. The removal of perchlorate by various adsorbents was studied. A cationic organoclay (TC-99) exhibited effective removal of perchlorate from drinking water matrices.

  13. The Impact of Temperature on Anaerobic Biological Perchlorate Treatment (United States)

    A 20-month pilot-scale study was conducted to examine the impact of temperature on the performance of an anaerobic biological contactor used to treat perchlorate-contaminated water. The contactor was successfully acclimated with indigenous micro-organisms. Influent temperatures...


    The U.S. Environmental Protection Agency undertook at 3 ½ year pilot-scale biological perchlorate treatment study that included two long (311 and 340 days) examinations of anaerobic effluent polishing. The polishing system consisted of hydrogen peroxide addition and aeration, fo...

  15. Structure of aqueous sodium perchlorate solutions. (United States)

    General, Ignacio J; Asciutto, Eliana K; Madura, Jeffry D


    Salt solutions have been the object of study of many scientists through history, but one of the most important findings came along when the Hofmeister series were discovered. Their importance arises from the fact that they influence the relative solubility of proteins, and solubility is directly related to one of today's holy grails: protein folding. In this work we characterize one of the more-destabilizing salts in the series, sodium perchlorate, by studying it as an aqueous solution at various concentrations ranging from 0.08 to 1.60 mol/L. Molecular dynamics simulations at room temperature permitted a detailed study of the organization of solvent and cosolvent, in terms of its radial distribution functions, along with the study of the structure of hydrogen bonds in the ions' solvation shells. We found that the distribution functions have some variations in their shape as concentration changes, but the position of their peaks is mostly unaffected. Regarding water, the most salient fact is the noticeable (although small) change in the second hydration shell and even beyond, especially for g(O(w)***O(w)), showing that the locality of salt effects should not be restricted to considerations of only the first solvation shell. The perturbation of the second shell also appears in the study of the HB network, where the difference between the number of HBs around a water molecule and around the Na(+) cation gets much smaller as one goes from the first to the second solvation shell, yet the difference is not negligible. Nevertheless, the effect of the ions past their first hydration shell is not enough to make a noticeable change in the global HB network. The Kirkwood-Buff theory of liquids was applied to our system, in order to calculate the activity derivative of the cosolvent. This coefficient, along with a previously calculated preferential binding, allowed us to establish that if a folded AP peptide is immersed in the studied solution, becoming the solute, then

  16. Nitrate and Perchlorate removal from groundwater by ion exchange

    Energy Technology Data Exchange (ETDEWEB)

    Burge, S; Halden, R


    This study was conducted to evaluate the performance of a small scale ion exchange unit (Krudico, Inc of Auborn, IA) for removal of nitrate and perchlorate from groundwater at Lawrence Livermore National Laboratory's Site 300. The unit was able to treat 3,600 gallons of Site 300 groundwater, at an average influent concentration of 100 mg/L NO{sub 3}{sup -} before breakthrough occurred. The unit contained 2.5 ft{sup 3} of Sybron SR-7 resin. Seventy gallons of regeneration waste were generated (water treated to waste ratio of 51:1). The effluent concentration was about 20 mg/L NO{sub 3}{sup -}, which is equivalent to a treatment efficiency of at least 80%. There are several options for implementing this technology at Site 300. A target well, in the 817 area, has been selected. It has a 3 to 4 gpm flow rate, and concentrations of 90 mg/L NO{sub 3}{sup -} and 40 {micro}g/L perchlorate. The different treatment options include ion exchange treatment of nitrate only, nitrate and perchlorate, or perchlorate only. Option 1: For the treatment of nitrate only, this unit will be able to treat 3,700 gallons of water before regeneration is required. If both columns of the ion exchange unit are used, 7,400 gallons could be treated before the columns will need to be regenerated (producing 140 gallons of waste, per cycle or every 1.5 days). The effluent nitrate concentration is expected to be about 17 mg/L. Annual operation and maintenance costs are estimated to be $0.14 per gallon of water treated. Option 2: If only perchlorate is to be removed with ion exchange at the 817 area, a smaller unit should be considered. A 55 gallon canister filled with ion exchange resin should be able to reduce perchlorate concentrations in the groundwater from 40 {micro}g/L to non-detect levels for three years before the resin would need to be replaced. The contaminant-laden resin would be disposed of as hazardous waste. It is not practical to regenerate the resin because of the extreme

  17. Thyroid function and reproductive success in rodents exposed to perchlorate via food and water. (United States)

    Smith, Philip N; Severt, Scott A; Jackson, J W Andrew; Anderson, Todd A


    The purpose of the present study was to determine if exposure to perchlorate via food items would have effects on mammals similar to those caused by exposure through drinking water at approximately equivalent doses. Prairie voles (Microtus ochrogaster) and deer mice (Peromyscus maniculatus) were used to assess the potential toxicity of perchlorate-contaminated food items. Voles and mice were divided randomly into three treatment groups--perchlorate-contaminated food (PCF), perchlorate-contaminated water (PCW), and control groups--such that each treatment group contained equal numbers of males and females. Rodents in PCF treatment groups were fed chow formulated with soybean plant matter that had been grown with perchlorate-contaminated irrigation water. Individuals in the control and PCF groups were provided distilled/deionized drinking water, whereas the PCW group received drinking water containing sodium perchlorate. Only slight differences among treatment groups were observed in a variety of endpoints, including reproductive success, tissue perchlorate concentrations, thyroid hormone concentrations, and thyroid histology. However, trends observed in the present study suggest that perchlorate exposure via water may result in slightly greater effects than exposure to perchlorate via food. These data and recent reports of perchlorate in a wide variety of food items indicate that exposure via food intake is an important consideration when examining cumulative risk among humans, livestock, and wildlife.

  18. 21 CFR 184.1138 - Ammonium chloride. (United States)


    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ammonium chloride. 184.1138 Section 184.1138 Food... Specific Substances Affirmed as GRAS § 184.1138 Ammonium chloride. (a) Ammonium chloride (NH4Cl, CAS Reg. No. 12125-02-9) is produced by the reaction of sodium chloride and an ammonium salt in solution....

  19. 21 CFR 184.1133 - Ammonium alginate. (United States)


    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ammonium alginate. 184.1133 Section 184.1133 Food... Specific Substances Affirmed as GRAS § 184.1133 Ammonium alginate. (a) Ammonium alginate (CAS Reg. No. 9005.... Ammonium alginate is prepared by the neutralization of purified alginic acid with appropriate pH...

  20. Sensitivity and adaptability of methanogens to perchlorates: Implications for life on Mars (United States)

    Kral, Timothy A.; Goodhart, Timothy H.; Harpool, Joshua D.; Hearnsberger, Christopher E.; McCracken, Graham L.; McSpadden, Stanley W.


    In 2008, the Mars Phoenix Lander discovered perchlorate at its landing site, and in 2012, the Curiosity rover confirmed the presence of perchlorate on Mars. The research reported here was designed to determine if certain methanogens could grow in the presence of three different perchlorate salt solutions. The methanogens tested were Methanothermobacter wolfeii, Methanosarcina barkeri, Methanobacterium formicicum and Methanococcus maripaludis. Media were prepared containing 0%, 0.5%, 1.0%, 2%, 5% and 10% wt/vol magnesium perchlorate, sodium perchlorate, or calcium perchlorate. Organisms were inoculated into their respective media followed by incubation at each organism's growth temperature. Methane production, commonly used to measure methanogen growth, was measured by gas chromatography of headspace gas samples. Methane concentrations varied with species and perchlorate salt tested. However, all four methanogens produced substantial levels of methane in the presence of up to 1.0% perchlorate, but not higher. The standard procedure for growing methanogens typically includes sodium sulfide, a reducing agent, to reduce residual molecular oxygen. However, the sodium sulfide may have been reducing the perchlorate, thus allowing for growth of the methanogens. To investigate this possibility, experiments were conducted where stainless steel nails were used instead of sodium sulfide as the reducing agent. Prior to the addition of perchlorate and inoculation, the nails were removed from the liquid medium. Just as in the prior experiments, the methanogens produced methane at comparable levels to those seen with sodium sulfide as the reductant, indicating that sodium sulfide did not reduce the perchlorate to any significant extent. Additionally, cells metabolizing in 1% perchlorate were transferred to 2%, cells metabolizing in 2% were transferred to 5%, and finally cells metabolizing in 5% were transferred to 10%. All four species produced methane at 2% and 5%, but not 10

  1. Relative source contributions for perchlorate exposures in a lactating human cohort

    Energy Technology Data Exchange (ETDEWEB)

    Kirk, Andrea B. [University of North Texas Health Sciences Center (United States); Dyke, Jason V. [University of Texas at Arlington (United States); Ohira, Shin-Ichi [Kumamoto University (Japan); Dasgupta, Purnendu K., E-mail: [University of Texas at Arlington (United States)


    Perchlorate is an iodine-uptake inhibitor and common contaminant of food and drinking water. Understanding the amount of perchlorate exposure occurring through non-water sources is essential for accurate estimates of human exposure levels, and establishment of drinking water limits for this pervasive contaminant. The study objective was to determine the amount of perchlorate intake derived from diet rather than water. Subjects provided drinking water samples, detailed fluid-intake records, 24 h urine collections and four milk samples for nine days. Samples were analyzed for perchlorate by isotope dilution ion chromatography–tandem mass spectrometry. Amounts of perchlorate derived from drinking water and dietary sources were calculated for each individual. Water of local origin was found to contribute a minor fraction of perchlorate intake. Estimated fraction intake from drinking water ranged from 0 to 36%. The mean and median dose of perchlorate derived from non-water sources by lactating women was 0.18 μg/kg/day (range: 0.06 to 0.36 μg/kg/day.) Lactating women consumed more fluid (mean 2.424 L/day) than has been assumed in recent risk assessments for perchlorate. The data reported here indicate that lactating women may be exposed to perchlorate through dietary sources at markedly higher levels than estimated previously. Exposures to perchlorate from non-water sources may be higher than recent estimates, including those used to develop drinking water standards. - Highlights: ► Residence in an area with perchlorate-contaminated water may be a poor predictor of exposure. ► Exposures to perchlorate from food are likely underestimated. ► The relative contributions for human perchlorate exposures should be weighted more heavily towards non-water sources.

  2. Environmental impacts of perchlorate with special reference to fireworks--a review. (United States)

    Sijimol, M R; Mohan, Mahesh


    Perchlorate is an inorganic anion that is used in solid rocket propellants, fireworks, munitions, signal flares, etc. The use of fireworks is identified as one of the main contributors in the increasing environmental perchlorate contamination. Although fireworks are displayed for entertainment, its environmental costs are dire. Perchlorates are also emerging as potent thyroid disruptors, and they have an impact on the ecology too. Many studies have shown that perchlorate contaminates the groundwater and the surface water, especially in the vicinity of fireworks manufacturing sites and fireworks display sites. The health and ecological impacts of perchlorate released in fireworks are yet to be fully assessed. This paper reviews fireworks as a source of perchlorate contamination and its expected adverse impacts.


    Energy Technology Data Exchange (ETDEWEB)

    Strietelmeier, E. A. (Elizabeth A.); Espinosa, Melissa L. (Melissa L.); Adams, J. D. (Joshua D. ); Leonard, P. A. (Patricia A.); Hodge, E. M. (Evangeline M.)


    Research was conducted to evaluate a multiple-layer system of volcanic rock, limestone, Apatite mineral and a 'biobarrier' to impede migration of radionuclides, metals and colloids through shallow alluvial groundwater, while simultaneously destroying contaminants such as nitrate and perchlorate. The 'bio' portion of this Multi-Barrier system uses highly porous, slowly degradable, carbon-based material (pecan shells) that serves as an energy source and supports the growth of indigenous microbial populations capable of destroying biodegradable compounds. The studies, using elevated nitrate concentrations in groundwater, have demonstrated reduction from levels of 6.5-9.7 mM nitrate (400-600 mg/L) to below discharge limits (0.16 mM nitrate). Perchlorate levels of 4.3 {micro}M (350 {micro}g/L) were also greatly reduced. Elevated levels of nitrate in drinking water are a public health concern, particularly for infants and adults susceptible to gastric cancer. Primary sources of contamination include feedlots, agriculture (fertilization), septic systems, mining and nuclear operations. A major source of perchlorate contamination in water is ammonium perchlorate from manufacture/use of rocket propellants. Perchlorate, recently identified as an EPA contaminant of concern, may affect thyroid function and cause tumor formation. A biobarrier used to support the growth of microbial populations (i.e. a biofilm) is a viable and inexpensive tool for cleaning contaminated groundwater. Aquatic ecosystems and human populations worldwide are affected by contaminated water supplies. One of the most frequent contaminants is nitrate. Remediation of nitrate in groundwater and drinking water by biodegradation is a natural solution to this problem. Microbial processes play an extremely important role in in situ groundwater treatment technologies. The assumption of carbon limitation is the basis for addition of carbon-based substrates to a system in the development of

  4. A Potential Mechanism for Perchlorate Formation on Mars: Surface-Radiolysis-Initiated Atmospheric Chemistry (United States)

    Wilson, Eric; Atreya, Sushil K.; Kaiser, Ralf-Ingo; Mahaffy, Paul


    Perchlorate (ClO4-) is prevalent on Earth, and with observations of perchlorate on lunar samples and chondrite meteorites, along with recent observations indicating the presence of perchlorate (ClO4-) in the Martian surface by the Phoenix lander and the Sample Analysis at Mars (SAM) on the Mars Science Laboratory (MSL) rover, it appears that the existence of perchlorate is widespread throughout the solar system. However, the abundance and isotopic composition of Martian perchlorate suggest that the perchlorate formation mechanism on Mars may involve a different path than perchlorate found elsewhere in the solar system. Motivated by this, we employ a one-dimensional chemical model to investigate the viability of perchlorate formation in the atmosphere of Mars, instigated by the radiolysis of the Martian surface by galactic cosmic rays. The surface-atmosphere interaction to produce Martian perchlorate involves the sublimation of chlorine oxides into the atmosphere, through surface radiolysis, and their subsequent synthesis to form perchloric acid (HClO4), followed by surface deposition and mineralization to form surface perchlorates. Considering the chlorine oxide, OClO, we find an OClO surface flux as low as 3.2x107 molecules cm-2 s-1, sublimated into the atmosphere from the surface could produce sufficient HClO4 to explain the perchlorate concentration on Mars, assuming an accumulation depth of 30 cm and integrated over the Amazonian period. Radiolysis provides an efficient pathway for the oxidation of chlorine, bypassing the efficient Cl/HCl recycling mechanism that characterizes HClO4 formation mechanisms proposed for the Earth but not Mars.

  5. Evaluation of Potential for Monitored Natural Attenuation of Perchlorate in Groundwater (United States)


    Perchlorate-Impacted Groundwater for Base Case 8-4 Cost Components for Extraction and Treatment of Perchlorate-Impacted Groundwater for Base Case 8-5...consumed, increasing the likelihood of perchlorate biodegradation in the natural environment (Coates and Jackson, 2009). Trace amounts of molybdenum are...chlorinated solvents (USEPA, 1998) have been in use for many years. These documents describe systematic steps for delineating contaminant plumes

  6. Parameters for the Pyrolysis of Organic Material - Perchlorate Mixtures (United States)

    Steininger, Harald; Goesmann, Fred; Goetz, Walter


    The ESA-lead Mars rover ExoMars (launch in 2018) will carry a suit of instruments, one of the in-struments is the Mars Organic Molecule Analyzer MOMA. Organic material in the Martian soil will be either pyrolyzed at temperatures of up to 1000°C and separated by gas chromatography or volatilized with the help of an UV-laser. A mass spectrometer will be the detector for both methods. Chlorinated organics have been detected in pyroly-sis GC-MS experiments on Mars two times. The first time during the Viking mission in 1976 and a second time with the Sample Analysis on Mars (SAM) in-strument onboard the Curiosity rover in 2012. [1] [2] The presence of perchlorates found by the Phoenix mission in 2008 [3] lead to the discovery that organic molecules not only get oxidized during pyrolysis, but also chlorinated organic compounds can be pro-duced. [4] The parameters used for pyrolysis and the sample composition especially the distribution of organics and perchlorates within the sample and the concentrations of organics and perchlorate have a huge influence on the products created. It is possible to change the condi-tions of the pyrolysis by spatially separating the organ-ics from the perchlorates that the chloromethanes get the major product of the pyrolysis. This might help to understand the results of the (SAM) instrument yield-ing mono-, di- and trichloromethane and a chlorinated 4-hydrocarbon molecule. References: [1] Biemann K et al. (1977) JGR, 82, 4641-4658. [2] Grotzinger J. P et al. (2011) AGU Fall Meeting U13A-01 [3] Hecht M. H., et al. (2009) Science, 325 64-67. [4] Steininger H., Goesmann F., Goetz W. (2011) Planet. & Space Sci., 71, 9-17. Acknowledgments: This work was funded by DLR (FKZ 50QX1001)

  7. Using Stable Isotope Ratio Analysis to Distinguish Perchlorate Sources (United States)


    Death Valley caliche West Texas OCl - + O 3 ClO 2 + O 3 -5.0 0.0 5.0 10 15 20 -30 -20 -10 0 10 20 30 40 50  1 7 O ( p e r m i l ) 18O (per mil...Synthetic solids Atacama caliche/ fertilizer Death Valley caliche West Texas OCl - + UV ClO 2 + UV Perchlorate generated with UV 36Cl Analysis Long

  8. 1-Benzylpiperazine-1,4-diium bis(perchlorate monohydrate

    Directory of Open Access Journals (Sweden)

    Kamel Kaabi


    Full Text Available In the title compound, C11H18N22+·2ClO4−·H2O, one perchlorate anion is disordered over two orientations in a 0.66 (3:0.34 (3 ratio. Intermolecular O—H...O, N—H...O and C—H...O hydrogen bonds link the cations, anions and water molecules into ribbons extending along [100].

  9. 4-(2-Azaniumylethylpiperazin-1-ium bis(perchlorate

    Directory of Open Access Journals (Sweden)

    Mohammad Reza Reisi


    Full Text Available In the title compound, C6H17N32+·2ClO4−, the piperazine ring adopts a chair conformation with the ethylammonium fragment occupying an equatorial position. In the crystal, the dications and perchlorate anions are linked through N—H...O hydrogen bonding and weak C—H...O hydrogen bonding into a three-dimensional supramolecular network.

  10. Influence of the ammonium salt anion on the synergistic solvent extraction of lanthanides with mixtures of thenoyltrifluoroacetone and tridecylamine

    Energy Technology Data Exchange (ETDEWEB)

    Dukov, I.L.; Jordanov, V.M. [Univ. of Chemical Technology and Metallurgy, Sofia (Bulgaria). Dept. of Inorganic Chemistry


    The synergistic solvent extraction of Pr, Gd and Yb with mixtures of thenoyltrifluoroacetone (HTTA) and primary ammonium salt (tridecylammonium chloride or perchlorate, TDAH(Cl, ClO{sub 4})) in C{sub 6}H{sub 6} has been studied. The composition of the extracted species have been determined as Ln(TTA){sub 3}TDAHA(A{sup {minus}} = Cl{sup {minus}} or ClO{sub 4}{sup {minus}}). The values of the equilibrium constant K{sub T,S} have been calculated. The influence of the ammonium salt anion on the extraction process has been discussed. The separation factors of the pairs Gd/Pr and Yb/Gd have been determined.

  11. Kinetics analysis of a salt-tolerant perchlorate-reducing bacterium: effects of sodium, magnesium, and nitrate. (United States)

    Xiao, Yeyuan; Roberts, Deborah J


    Salt-tolerant perchlorate-reducing bacteria can be used to regenerate ion-exchange brines or resins exhausted with perchlorate. A salt-tolerant perchlorate-reducing Marinobacter vinifirmus strain P4B1 was recently purified. This study determined the effects of Na(+) and Mg(2+) concentrations on the perchlorate reduction rate of P4B1. The results showed that strain P4B1 could utilize perchlorate and grow in the presence of 1.8% to 10.2% NaCl. Lower NaCl concentrations allowed faster perchlorate reduction. The addition of Mg(2+) to the culture showed significant effects on perchlorate reduction when perchlorate was the sole electron acceptor. A molar Mg(2+)/Na(+) ratio of ∼0.11 optimized perchlorate degradation and cell growth. When perchlorate and nitrate were both present, nitrate reduction did not start significantly until perchlorate was below 100 mg/L. Tests with washed cell suspensions indicated that strain P4B1 had both perchlorate and nitrate reduction enzymes. When the culture was exposed to both perchlorate and nitrate, the nitrate reduction enzyme activity was low. The maximum specific substrate utilization rate (Vm) and the half saturation coefficient (KS) for P4B1 (30 g/L NaCl) determined in this study were 0.049 ± 0.003 mg ClO4(-)/mg VSS-h and 18 ± 4 mg ClO4(-)/L, respectively.

  12. Validation of Chlorine and Oxygen Isotope Ratio Analysis To Differentiate Perchlorate Sources and To Document Perchlorate Biodegradation (United States)


    ferrous iron, sulfite, or thiosulfate (Brown and Gu, 2006; Urbansky, 2002). ClO4- reduction can be mediated by some catalysts , including ruthenium(II... nitrate reduction by denitrifying bacteria. Limnol. Oceanography 53:2533-2545. Granger, J.; Sigman, D.M.; Needoba, J.A.; Harrison, P.J. 2004. Coupled... nitrate reduction pathways are separately induced in the perchlorate-respiring bacterium Dechlorosoma sp. KJ and the chlorate-respiring bacterium

  13. Perchlorate in the Hydrologic Cycle - An Overview of Sources and Occurrence (United States)

    Stonestrom, D. A.; Jackson, W.; Mayer, K.; Orris, G. J.


    Perchlorate (ClO4-) in water and food is of concern due to deleterious health affects associated with hypothyroidism. The presence of widespread perchlorate in 0-to-28 ka-old pristine ground water of the Middle Rio Grande Basin (Plummer et al., 2006, ES&T, DOI:10.1021/es051739h), in ground water >1 mile from agricultural activities in the Southern High Plains (Rajagapolan et al., 2006, ES&T, DOI:10.1021/es052155i), and in unsaturated zones throughout the arid and semiarid southwestern United States (Rao et al., 2007, ES&T, DOI:10.1021/es062853i) clearly indicates that perchlorate is a non-exotic component of the hydrologic cycle, at least in dry environments. The natural system has been greatly perturbed in places by human activities. Most anthropogenic inputs are associated with the manufacture and use of explosives and rocket fuel, providing concentrated sources of excess perchlorate to the hydrologic cycle. Perchlorate-containing fertilizers and irrigation provide dispersed sources within and down-gradient from agricultural areas. Natural sources include photochemically mediated reactions involving ozone at the land surface and in the lower atmosphere. A growing body of work indicates that a small, but persistent, meteoric source acting over thousands of years can explain observed accumulations of unsaturated-zone perchlorate in arid regions. In addition to meteoric sources, oxyanions produced during volcanogenic processes can include appreciable amounts of natural perchlorate. Terrestrial plants take up perchlorate in soil water, with some species of xerophytic succulents concentrating the anion to high levels. Similarly, perchlorate in marine plants indicates that perchlorate is part of marine biochemical cycles. Perchlorate-bearing marine sediments of late Tertiary age suggest that perchlorate has been part of global geochemical cycles for millions of years and, furthermore, can be preserved in the subsurface despite the nearly ubiquitous presence of

  14. Portable Amperometric Perchlorate Selective Sensors with Microhole Array-water/organic Gel Interfaces

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Sang Hyuk; Girault, Hubert H.; Lee, Hye Jin [Kyungpook National Univ., Daegu (Korea, Republic of); Kim, Hyungi [Gyeongbuk Technopark, Gyeongsan (Korea, Republic of); Girault, Hubert H. [Ecole Polytechnique Federale de Lausanne, Lausanne (Switzerland)


    A novel stick-shaped portable sensing device featuring a microhole array interface between the polyvinylchloride-2-nitrophenyloctylether (PVC-NPOE) gel and water phase was developed for in-situ sensing of perchlorate ions in real water samples. Perchlorate sensitive sensing responses were obtained based on measuring the current changes with respect to the assisted transfer reaction of perchlorate ions by a perchlorate selective ligand namely, bis(dibenzoylmethanato)Ni(II) (Ni(DBM){sub 2}) across the polarized microhole array interface. Cyclic voltammetry was used to characterize the assisted transfer reaction of perchlorate ions by the Ni(DBM){sub 2} ligand when using the portable sensing device. The current response for the transfer of perchlorate anions by Ni(DBM){sub 2} across the micro-water/gel interface linearly increased as a function of the perchlorate ion concentration. The technique of differential pulse stripping voltammetry was also utilized to improve the sensitivity of the perchlorate anion detection down to 10 ppb. This was acquired by preconcentrating perchlorate anions in the gel layer by means of holding the ion transfer potential at 0 mV (vs. Ag/AgCl) for 30 s followed by stripping the complexed perchlorate ion with the ligand. The effect of various potential interfering anions on the perchlorate sensor was also investigated and showed an excellent selectivity over Br{sup -}, NO{sub 2}{sup -}, NO{sub 3}{sup -}, CO{sub 3}{sup 2-}, CH{sub 3}COO{sup -} and SO{sub 4}{sup 2-} ions. As a final demonstration, some regional water samples from the Sincheon river in Daegu city were analyzed and the data was verified with that of ion chromatography (IC) analysis from one of the Korean-certified water quality evaluation centers.

  15. 21 CFR 582.1141 - Ammonium phosphate. (United States)


    ... 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)...

  16. 76 FR 46907 - Ammonium Nitrate Security Program (United States)


    ... and fertilizer blends containing more than 15% by weight ammonium nitrate, except liquid fertilizers... concerning the detonability of ammonium nitrate; Comments on how likely ammonium nitrate fertilizer users would be to use an alternative fertilizer that is potentially less detonable, such as Sulf-N...

  17. 76 FR 11273 - Ammonium Nitrate From Russia (United States)


    ... COMMISSION Ammonium Nitrate From Russia AGENCY: United States International Trade Commission. ACTION: Institution of a five-year review concerning the suspended investigation on ammonium nitrate from Russia... investigation on ammonium nitrate from Russia would be likely to lead to continuation or recurrence of...

  18. 76 FR 47238 - Ammonium Nitrate From Russia (United States)


    ... COMMISSION Ammonium Nitrate From Russia Determination On the basis of the record \\1\\ developed in the subject... order on ammonium nitrate from Russia would be likely to lead to continuation or recurrence of material... Commission are contained in USITC Publication 4249 (August 2011), entitled Ammonium Nitrate from...

  19. 21 CFR 582.7133 - Ammonium alginate. (United States)


    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Ammonium alginate. 582.7133 Section 582.7133 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Ammonium alginate. (a) Product. Ammonium alginate. (b) Conditions of use. This substance is...

  20. Perchlorate in groundwater: a synoptic survey of "pristine" sites in the coterminous United States. (United States)

    Parker, David R; Seyfferth, Angelia L; Reese, Brandi Kiel


    Perchlorate is widely used as an oxidant in solid rocket propellants and energetic applications, and it has frequently been detected in groundwaters at concentrations relevant to human health. The possibility of naturally occurring perchlorate has only recently received significant attention. Relying primarily on domestic, agricultural, and recreational wells, we utilized a network of volunteers to help collect 326 groundwater samples from across the coterminous United States. Care was taken to avoid known, USEPA-documented sites of perchlorate use or release, as well as perchlorate contamination due to disinfection using hypochlorite. Using IC-ESI-MS and a Cl18O4- internal standard, we achieved a method detection limit (MDL) of 40 ng/L perchlorate and a minimum reporting level (MRL) of 120 ng/L. Of the 326 samples, 147 (45%) were below the MDL, while 42 (13%) were between the MDL and the MRL. Of the 137 samples that could be quantified, most (109) contained 10000 ng/L) previously reported for the west-central Texas area appear to be anomalous. Perchlorate concentrations were positively correlated with nitrate levels (P < 0.001) but not with chloride concentrations. Opportunities exist for follow-up studies of perchlorate's origins using isotope forensics and for further elucidation of the role of atmospheric processes in the formation or transport of perchlorate.

  1. Tailored Granular Activated Carbon Treatment of Perchlorate in Drinking Water. ESTCP Cost and Performance Report (United States)


    improvements in the perchlorate capacity and decreases in the market price of perchlorate selective IX resins, the operating cost of conventional...Representative Frank Lajutis Fontana Water Company 8440 Nuevo Avenue Fontana, CA 92335 Phone: (909) 822-2201, ext. 332 E-mail:

  2. Bifunctional lanthanum phosphate substrates as novel adsorbents and biocatalyst supports for perchlorate removal

    Energy Technology Data Exchange (ETDEWEB)

    Sankar, Sasidharan [Materials Science and Technology Division (India); Prajeesh, Gangadharan Puthiya Veetil; Anupama, Vijaya Nadaraja [Process Engineering and Environmental Technology Division, CSIR – National Institute for Interdisciplinary Science and Technology, Industrial Estate P.O., Thiruvananthapuram 695019 (India); Krishnakumar, Bhaskaran [Process Engineering and Environmental Technology Division, CSIR – National Institute for Interdisciplinary Science and Technology, Industrial Estate P.O., Thiruvananthapuram 695019 (India); Academy of Scientific and Industrial Research (AcSIR) (India); Hareesh, Padinhattayil [Materials Science and Technology Division (India); Nair, Balagopal N. [R and D Centre, Noritake Co. Ltd., Aichi (Japan); Warrier, Krishna Gopakumar [Materials Science and Technology Division (India); Academy of Scientific and Industrial Research (AcSIR) (India); Hareesh, Unnikrishnan Nair Saraswathy, E-mail: [Materials Science and Technology Division (India); Academy of Scientific and Industrial Research (AcSIR) (India)


    Graphical abstract: Porous lanthanum phosphate substrates, obtained by an environmentally benign thermal gelation process, performed the role of dual functional sorbent facilitating perchlorate adsorption and bioremediation through the growth of perchlorate reducing microbial colonies. - Highlights: • Lanthanum phosphate monoliths as efficient perchlorate adsorbents. • And also as substrates for biofilm (perchlorate reducing bacteria) growth. • Environmentally benign thermal gelation process for substrate fabrication. • 98% adsorption efficiency for perchlorate concentrations up to 100 μg/L. • The regenerated monoliths show nearly 100% reusability. - Abstract: Porous lanthanum phosphate substrates, obtained by an environmentally benign colloidal forming process employing methyl cellulose, are reported here as excellent adsorbents of perchlorate with >98% efficiency and with 100% reusability. Additionally, the effectiveness of such substrates as biocatalyst supports that facilitate biofilm formation of perchlorate reducing microbes (Serratia marcescens NIIST 5) is also demonstrated for the first time. The adsorption of perchlorate ions is attributed to the pore structure of lanthanum phosphate substrate and the microbial attachment is primarily ascribed to its intrinsic hydrophobic property. Lanthanum phosphate thus emerges as a dual functional material that possesses an integrated adsorption/bioremediation property for the effective removal of ClO{sub 4}{sup −} which is an increasingly important environmental contaminant.

  3. Perchlorate and halophilic prokaryotes: implications for possible halophilic life on Mars. (United States)

    Oren, Aharon; Elevi Bardavid, Rahel; Mana, Lily


    In view of the finding of perchlorate among the salts detected by the Phoenix Lander on Mars, we investigated the relationships of halophilic heterotrophic microorganisms (archaea of the family Halobacteriaceae and the bacterium Halomonas elongata) toward perchlorate. All strains tested grew well in NaCl-based media containing 0.4 M perchlorate, but at the highest perchlorate concentrations, tested cells were swollen or distorted. Some species (Haloferax mediterranei, Haloferax denitrificans, Haloferax gibbonsii, Haloarcula marismortui, Haloarcula vallismortis) could use perchlorate as an electron acceptor for anaerobic growth. Although perchlorate is highly oxidizing, its presence at a concentration of 0.2 M for up to 2 weeks did not negatively affect the ability of a yeast extract-based medium to support growth of the archaeon Halobacterium salinarum. These findings show that presence of perchlorate among the salts on Mars does not preclude the possibility of halophilic life. If indeed the liquid brines that may exist on Mars are inhabited by salt-requiring or salt-tolerant microorganisms similar to the halophiles on Earth, presence of perchlorate may even be stimulatory when it can serve as an electron acceptor for respiratory activity in the anaerobic Martian environment.


    Interest in possible sources of perchlorate (ClO4-) that could lead to environmental release has been heightened since the EPA placed this anion on its Contaminant Candidate List (CCL) for drinking water. Besides its association with defense and aerospace activities, perchlorate ...

  5. Hybrid Adsorption-Membrane Biological Reactors for Improved Performance and Reliability of Perchlorate Removal Processes (United States)


    carbon supply for the autotrophic perchlorate reducing bacteria. The membrane used in the reactor is a hollow-fiber microfiltration membrane made from...1 HYBRID ADSORPTION- MEMBRANE BIOLOGICAL REACTORS FOR IMPROVED PERFORMANCE AND RELIABILITY OF PERCHLORATE REMOVAL PROCESSES L.C. Schideman...Center Champaign, IL 61826, USA ABSTRACT This study introduces the novel HAMBgR process (Hybrid Adsorption Membrane Biological Reactor) and

  6. Anaerobic Treatment of Wastewaters Containing Perchlorate from Munitions Handling and Production (United States)


    1 Background ...ERDC/CERL TR-08-3 1 1 Introduction Background Perchlorate is an oxidant that is widely used in propellants such as solid rocket motors, and in...result in hypothyroidism , mental retardation, and speech and hearing degradation. Treatment technology Perchlorate treatment technologies are

  7. Photodimerization and photooxygenation of 9-vinylcarbazole catalyzed by titanium dioxide and magnesium perchlorate

    Institute of Scientific and Technical Information of China (English)

    Hajime; Maeda; Mio; Yamamoto; Hideyuki; Nakagawa; Kazuhiko; Mizuno


    Photoreaction of 9-vinylcarbazole in acetonitrile in the presence of titanium dioxide and a catalytic amount of magnesium perchlorate gave 3,6-di(9-carbazolyl)-1,2-dioxane as a photooxygenated product via photodimerization of 9-vinylcarbazole.The photoreaction proceeds via an electron transfer mechanism,where magnesium perchlorate accelerated formation of the photo-oxygenated product.

  8. Thermal decomposition of ammonium perchlorate—A TGA–FTIR–MS study: Part I

    Energy Technology Data Exchange (ETDEWEB)

    Mallick, Lovely; Kumar, Sudarshan [Department of Aerospace Engineering, Indian Institute of Technology, Bombay, Mumbai 400076 (India); Chowdhury, Arindrajit, E-mail: [Department of Mechanical Engineering Indian Institute of Technology, Bombay, Mumbai 400076 (India)


    Highlights: • TGA–FTIR–MS study of ammonium perchlorate. • Decomposition was divided into low, intermediate, and high temperature regimes. • N{sub 2}O and NO{sub 2} were the major species at low and high temperature regimes, respectively. • N{sub 2}O, NO{sub 2}, HNO{sub 3}, and HCl were quantified to aid kinetic evaluation. • NO was not detected as a major product at any stage. - Abstract: The thermal decomposition of ammonium perchlorate has been studied using thermogravimetric analysis (TGA), coupled with Fourier transform infrared (FTIR) spectroscopy and electron ionization (EI) mass spectrometry (MS) of the evolved gases. The thermal decomposition could be demarcated into three distinct regimes, the low temperature decomposition (LTD) regime and the high temperature decomposition (HTD) regime, with an intermediate regime between the two, named as the intermediate temperature decomposition (ITD) regime. Using FTIR spectroscopy, N{sub 2}O was detected as the primary species during the LTD regime, followed by HCl, NO{sub 2}, and HNO{sub 3}, in lesser quantities. On the contrary, NO{sub 2} was found to be the principal species, followed by almost equal concentrations of HCl, N{sub 2}O, and HNO{sub 3} in the HTD regime. Other important species, such as H{sub 2}O, Cl{sub 2}, O{sub 2}, etc., although observed by MS, were not quantified. NO could not be identified in appreciable quantities in any of the regimes. Based on the species detected during the present work, and previous research, a reaction scheme has been proposed for AP decomposition in the LTD and the HTD regimes.

  9. The impact of temperature on the performance of anaerobic biological treatment of perchlorate in drinking water. (United States)

    Dugan, Nicholas R; Williams, Daniel J; Meyer, Maria; Schneider, Ross R; Speth, Thomas F; Metz, Deborah H


    A 20-month pilot-scale study was conducted to examine the impact of temperature on the performance of an anaerobic biological contractor used to treat perchlorate-contaminated water. The contractor was successfully acclimated with indigenous microorganisms. Influent temperatures varied from 1.4 to 30 degrees C. The objectives of the study were to investigate the effects of temperature on perchlorate removal, nitrate removal, nitrite formation, dissolved oxygen consumption, sulfide production, and nutrient acetate consumption. The results confirmed that consistent biological perchlorate removal to 2 microg /L is feasible at temperatures above 10 degrees C. Effluent concentrations of perchlorate, nitrate, and dissolved oxygen varied inversely with temperature, while sulfide varied positively with temperature. Under the conditions that prevailed during this study, 10 degrees C was a threshold temperature below which microbial activity, including perchlorate reduction, decreased dramatically.

  10. Phase diagram of ammonium nitrate (United States)

    Dunuwille, M.; Yoo, C. S.


    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.

  11. Specific adsorption of perchlorate anions on Pt{hkl} single crystal electrodes. (United States)

    Attard, Gary A; Brew, Ashley; Hunter, Katherine; Sharman, Jonathan; Wright, Edward


    The voltammetry of Pt{111}, Pt{100}, Pt{110} and Pt{311} single crystal electrodes as a function of perchloric acid concentration (0.05-2.00 M) has been studied in order to test the assertion made in recent reports by Watanabe et al. that perchlorate anions specifically adsorb on polycrystalline platinum. Such an assertion would have significant ramifications for our understanding of electrocatalytic processes at platinum surfaces since perchlorate anions at low pH have classically been assumed not to specifically adsorb. For Pt{111}, it is found that OHad and electrochemical oxide states are both perturbed significantly as perchloric acid concentration is increased. We suggest that this is due to specific adsorption of perchlorate anions competing with OHad for adsorption sites. The hydrogen underpotential deposition (H UPD) region of Pt{111} however remains unchanged although evidence for perchlorate anion decomposition to chloride on Pt{111} is reported. In contrast, for Pt{100} no variation in the onset of electrochemical oxide formation is found nor any shift in the potential of the OHad state which normally results from the action of specifically adsorbing anions. This suggests that perchlorate anions are non-specifically adsorbed on this plane although strong changes in all H UPD states are observed as perchloric acid concentration is increased. This manifests itself as a redistribution of charge from the H UPD state situated at more positive potential to the one at more negative potential. For Pt{110} and Pt{311}, marginal changes in the onset of electrochemical oxide formation are recorded, associated with specific adsorption of perchlorate. Specific adsorption of perchlorate anions on Pt{111} is deleterious to electrocatalytic activity in relation to the oxygen reduction reaction (ORR) as measured using a rotating disc electrode (RDE) in a hanging meniscus configuration. This study supports previous work suggesting that a large component of the ORR

  12. Palladium(II)-catalyzed oxidation of L-tryptophan by hexacyanoferrate(III) in perchloric acid medium: a kinetic and mechanistic approach

    Indian Academy of Sciences (India)

    Ahmed Fawzy


    The catalytic effect of palladium(II) on the oxidation of L-tryptophan by potassium hexacyanoferrate( III) has been investigated spectrophotometrically in aqueous perchloric acid medium. A first order dependence in [hexacyanoferrate(III)] and fractional-first order dependences in both [L-tryptophan] and [palladium(II)] were obtained. The reaction exhibits fractional-second order kinetics with respect to [H+]. Reaction rate increased with increase in ionic strength and dielectric constant of the medium. The effect of temperature on the reaction rate has also been studied and activation parameters have been evaluated and discussed. Initial addition of the reaction product, hexacyanoferrate(II), does not affect the rate significantly. A plausible mechanistic scheme explaining all the observed kinetic results has been proposed. The final oxidation products are identified as indole-3-acetaldehyde, ammonium ion and carbon dioxide. The rate law associated with the reaction mechanism is derived.

  13. 高氯酸铵的制备与工艺概况%Preparation and technology of ammonium perchlorate

    Institute of Scientific and Technical Information of China (English)




  14. Ballistic properties and burning behaviour of an ammonium perchlorate/guanidine nitrate/sodium nitrate airbag solid propellant

    Energy Technology Data Exchange (ETDEWEB)

    A. Ulas; G.A. Risha; K.K. Kuo [Middle East Technical University, Ankara (Turkey). Department of Mechanical Engineering


    An experimental investigation on the determination of ballistic properties and burning behavior of a composite solid propellant for airbag application was conducted. The experimental results were obtained using a high-pressure optical strand burner. Steady-state burning rates were determined for a pressure range of 20.8-41.5 MPa and initial propellant temperatures of -30 to +80{sup o}C. For the pressure and temperature ranges tested, the temperature sensitivity was on the order of 1 x 10{sup -3} K{sup -1}. The pressure exponent was found to be a function of the initial propellant temperature and was 0.75 at 25{sup o}C. The activation energy and the pre-exponential factor of the Arrhenius equation are 2.735 kcal/mol and 15.06 cm/s, respectively. The pressure deflagration limit for this propellant was found to be in the range of 8.37-8.72 MPa. During combustion, small condensed-phase spherical particles were ejected from the burning surface. The size of the particles decreased with either increasing the pressure or the initial propellant temperature. For pressures below 41.4 MPa, average particle size was on the order of 900 {mu}m, and at 84.4 MPa, the bead size was much smaller, on the order of 300 {mu}m. A chemical analysis on these particles using both the ESEM and the X-ray diffraction method indicated that the material of the beads was mostly sodium chloride with a small amount of silicon-containing compounds. 6 refs., 17 figs.

  15. Long-Range Transport of Perchlorate Observed in the Atmospheric Aerosols Collected at Okinawa Island, Japan (United States)

    Handa, D.; Okada, K.; Kuroki, Y.; Nakama, Y.; Nakajima, H.; Arakaki, T.; Tanahara, A.; Oomori, T.; Miyagi, T.; Kadena, H.; Ishizaki, T.; Nakama, F.


    The study of perchlorate has become quite active in the U.S. in the last several years. Perchlorate has been recognized as a new environmental pollutant and it attracted much attention quickly in the world. The health concern about perchlorate stems from the fact that it displaces iodide in the thyroid gland, while iodine-containing thyroid hormones are essential for proper neural development from the fetal stage through the first years of life. In this study, we determined the concentrations of perchlorate ion present in the atmospheric aerosols collected in Okinawa Island, Japan. We then examined the relationships between the perchlorate concentrations and the environmental parameters and the climatic conditions peculiar to Okinawa. Bulk aerosol samples were collected on quartz filters by using a high volume air sampler at Cape Hedo Atmosphere and Aerosol Monitoring Station (CHAAMS). Each sampling duration was one week. The quartz filters with aerosols were stirred with Milli-Q pure water for three hours before perchlorate ion was extracted. The extracted perchlorate ion concentrations were determined by ion chromatography (ICS-2000, DIONEX). The mean perchlorate concentration for the samples collected at CHAAMS was 1.83 ng/m3, and the minimum was 0.18 ng/m3. The samples collected during November 21-27, 2005, January 23-30, 2006 and April 24-01, 2006 had highest perchlorate concentrations. For these three samples, we performed back trajectory analysis, and found that the air mass for the three samples arrived from the Asian continent. A relatively strong correlation (r2 = 0.55) was found between perchlorate and nss-sulfate concentrations for the CHAAMS samples. Furthermore, we analyzed perchlorate in the soils and the fertilizers used for sugar cane farming around the CHAAMS area. The Milli-Q extract of the soil and the fertilizers did not contain any detectable levels of perchlorate ions. Therefore, it was suggested that perchlorate found in the atmospheric

  16. High pressure structural, elastic and vibrational properties of green energetic oxidizer ammonium dinitramide (United States)

    Yedukondalu, N.; Ghule, Vikas D.; Vaitheeswaran, G.


    Ammonium DiNitramide (ADN) is one of the most promising green energetic oxidizers for future rocket propellant formulations. In the present work, we report a detailed theoretical study on structural, elastic, and vibrational properties of the emerging oxidizer under hydrostatic compression using various dispersion correction methods to capture weak intermolecular (van der Waals and hydrogen bonding) interactions. The calculated ground state lattice parameters, axial compressibilities, and equation of state are in good accord with the available experimental results. Strength of intermolecular interactions has been correlated using the calculated compressibility curves and elastic moduli. Apart from this, we also observe discontinuities in the structural parameters and elastic constants as a function of pressure. Pictorial representation and quantification of intermolecular interactions are described by the 3D Hirshfeld surfaces and 2D finger print maps. In addition, the computed infra-red (IR) spectra at ambient pressure reveal that ADN is found to have more hygroscopic nature over Ammonium Perchlorate (AP) due to the presence of strong hydrogen bonding. Pressure dependent IR spectra show blue- and red-shift of bending and stretching frequencies which leads to weakening and strengthening of the hydrogen bonding below and above 5 GPa, respectively. The abrupt changes in the calculated structural, mechanical, and IR spectra suggest that ADN might undergo a first order structural transformation to a high pressure phase around 5-6 GPa. From the predicted detonation properties, ADN is found to have high and low performance characteristics (DCJ = 8.09 km/s and PCJ = 25.54 GPa) when compared with ammonium based energetic oxidizers (DCJ = 6.50 km/s and PCJ = 17.64 GPa for AP, DCJ = 7.28 km/s and PCJ = 18.71 GPa for ammonium nitrate) and well-known secondary explosives for which DCJ = ˜8-10 km/s and PCJ = ˜30-50 GPa, respectively.

  17. The relationship between perchlorate in drinking water and cord blood thyroid hormones: First experience from Iran

    Directory of Open Access Journals (Sweden)

    Ashraf Javidi


    Full Text Available Background: Considering the controversial information regarding the effects of perchlorate on thyroid function of high risk population as neonates, and given the high prevalence rate of thyroid disorders specially congenital hypothyroidism in our region, this study aims to investigate for the first time in Iran, the relationship between drinking groundwater perchlorate and cord blood thyroid hormones level in an industrial region. Methods: In this cross-sectional study, drinking groundwater perchlorate level of rural areas of Zarinshahr, Isfahan was measured. Simultaneously, cord blood level of thyroid hormones of neonates born in the studied region was measured. Thyroid function test of neonates in regions with low and high perchlorate level were compared. Results: In this study, 25 tap water samples were obtained for perchlorate measurement. Level of cord blood thyroid stimulating hormone (TSH, T4 and T3 of 25 neonates were measured. Mean (standard deviation of perchlorate, TSH, T4 and T3 was 3.59 (5.10 μg/l, 7.81 (4.14 mIU/m, 6.06 (0.85 mg/dl, and 63.46 (17.53 mg/dl, respectively. Mean levels of thyroid function tests were not different in low ( 0.05. Conclusions: Perchlorate did not appear to be related to thyroid function of neonates in the studied industrial region. It seems that iodine status of the regions, as well as other environmental contaminants and genetic background, could impact on its relation with thyroid function of neonates.

  18. Kinetics of nitrate and perchlorate removal and biofilm stratification in an ion exchange membrane bioreactor. (United States)

    Ricardo, Ana R; Carvalho, Gilda; Velizarov, Svetlozar; Crespo, João G; Reis, Maria A M


    The biological degradation of nitrate and perchlorate was investigated in an ion exchange membrane bioreactor (IEMB) using a mixed anoxic microbial culture and ethanol as the carbon source. In this process, a membrane-supported biofilm reduces nitrate and perchlorate delivered through an anion exchange membrane from a polluted water stream, containing 60 mg/L of NO₃⁻ and 100 μg/L of ClO₄⁻. Under ammonia limiting conditions, the perchlorate reduction rate decreased by 10%, whereas the nitrate reduction rate was unaffected. Though nitrate and perchlorate accumulated in the bioreactor, their concentrations in the treated water (2.8 ± 0.5 mg/L of NO₃⁻ and 7.0 ± 0.8 μg/L of ClO₄⁻, respectively) were always below the drinking water regulatory levels, due to Donnan dialysis control of the ionic transport in the system. Kinetic parameters determined for the mixed microbial culture in suspension showed that the nitrate reduction rate was 35 times higher than the maximum perchlorate reduction rate. It was found that perchlorate reduction was inhibited by nitrate, since after nitrate depletion perchlorate reduction rate increased by 77%. The biofilm developed in the IEMB was cryosectioned and the microbial population was analyzed by fluorescence in situ hybridization (FISH). The results obtained seem to indicate that the kinetic advantage of nitrate reduction favored accumulation of denitrifiers near the membrane, whereas per(chlorate) reducing bacteria were mainly positioned at the biofilm outer surface, contacting the biomedium. As a consequence of the biofilm stratification, the reduction of perchlorate and nitrate occur sequentially in space allowing for the removal of both ions in the IEMB.

  19. Perchlorate Exposure Reduces Primordial Germ Cell Number in Female Threespine Stickleback.

    Directory of Open Access Journals (Sweden)

    Ann M Petersen

    Full Text Available Perchlorate is a common aquatic contaminant that has long been known to affect thyroid function in vertebrates, including humans. More recently perchlorate has been shown to affect primordial sexual differentiation in the aquatic model fishes zebrafish and threespine stickleback, but the mechanism has been unclear. Stickleback exposed to perchlorate from fertilization have increased androgen levels in the embryo and disrupted reproductive morphologies as adults, suggesting that perchlorate could disrupt the earliest stages of primordial sexual differentiation when primordial germ cells (PGCs begin to form the gonad. Female stickleback have three to four times the number of PGCs as males during the first weeks of development. We hypothesized that perchlorate exposure affects primordial sexual differentiation by reducing the number of germ cells in the gonad during an important window of stickleback sex determination at 14-18 days post fertilization (dpf. We tested this hypothesis by quantifying the number of PGCs at 16 dpf in control and 100 mg/L perchlorate-treated male and female stickleback. Perchlorate exposure from the time of fertilization resulted in significantly reduced PGC number only in genotypic females, suggesting that the masculinizing effects of perchlorate observed in adult stickleback may result from early changes to the number of PGCs at a time critical for sex determination. To our knowledge, this is the first evidence of a connection between an endocrine disruptor and reduction in PGC number prior to the first meiosis during sex determination. These findings suggest that a mode of action of perchlorate on adult reproductive phenotypes in vertebrates, including humans, such as altered fecundity and sex reversal or intersex gonads, may stem from early changes to germ cell development.

  20. Synthesis of Chitosan Quaternary Ammonium Salts

    Institute of Scientific and Technical Information of China (English)


    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.

  1. Dissimilatory reduction of perchlorate and other common pollutants by a consortium enriched from tidal flats of the Yellow Sea

    Institute of Scientific and Technical Information of China (English)

    Nirmala Bardiya; Jae-Ho Bae


    Objective: To enrich a facultative anaerobic bacterial consortium from the Yellow Sea and assess its ability to reduce perchlorate and other co-pollutants. Methods: Bacterial consortium collected from the tidal flats of the Yellow Sea was enriched in an anoxic medium containing perchlorate as the electron (e-) acceptor and acetate as the electron (e-) donor. The enriched consortium was then tested for perchlorate reduction under different perchlorate concentrations and in the presence of nitrate by using standard anaerobic techniques. The complete enzymatic reduction of perchlorate to chloride was confirmed by chlorite dismutation. Ability of the consortium to grow with alternate e- acceptors was also tested with acetate as the e- donor. Results: The enriched consortium could rapidly reduce perchlorate up to the initial concentration of 25.65 mmol/L. In the presence of nitrate, perchlorate reduction did not occur immediately and reduction of nitrate started after a lag phase, with concomitant accumulation of nitrite. The perchlorate-enriched consortium could reduce chlorate, oxygen, Cr (VI), and selenate as the alternate e- acceptors but failed to utilize sulfate, thiosulfate, sulfite, and nitrite. Conclusions: The consortium from the tidal flats of the Yellow Sea could reduce perchlorate and co-contaminants such as chlorate, nitrate, Cr (VI), and selenate under heterotrophic conditions with acetate as the e- donor and carbon source. While perchlorate was completely dismutated into innocuous chloride and oxygen, accumulation of nitrite occurred during the reduction of nitrate.

  2. 49 CFR 176.410 - Division 1.5 materials, ammonium nitrate and ammonium nitrate mixtures. (United States)


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

  3. 33 CFR 126.28 - Ammonium nitrate, ammonium nitrate fertilizers, fertilizer mixtures, or nitro carbo nitrate... (United States)


    ... 33 Navigation and Navigable Waters 2 2010-07-01 2010-07-01 false Ammonium nitrate, ammonium nitrate fertilizers, fertilizer mixtures, or nitro carbo nitrate; general provisions. 126.28 Section 126...) WATERFRONT FACILITIES HANDLING OF DANGEROUS CARGO AT WATERFRONT FACILITIES § 126.28 Ammonium...

  4. The Impact of Temperature on the Performance of Anaerobic Biological Treatment of Perchlorate in Drinking Water (United States)

    A 20 month pilot-scale study was conducted to examine the impact of temperature on the performance of an anaerobic biological contactor used to treat perchlorate-contaminated water. The contactor was successfully acclimated with indigenous microorganisms. Influent temperatures ...


    Seven retail hydroponic nitrate fertilizer products, two liquid and five solid, were comparatively analyzed for the perchlorate anion (ClO4-) by ion chromatography (IC) with suppressed conductivity detection, complexation electrospray ionization mass spectrometry (cESI-MS), norma...

  6. Perchlorate: Health Effects and Technologies for Its Removal from Water Resources

    Directory of Open Access Journals (Sweden)

    Thiruvenkatachari Viraraghavan


    Full Text Available Perchlorate has been found in drinking water and surface waters in the United States and Canada. It is primarily associated with release from defense and military operations. Natural sources include certain fertilizers and potash ores. Although it is a strong oxidant, perchlorate is very persistent in the environment. At high concentrations perchlorate can affect the thyroid gland by inhibiting the uptake of iodine. A maximum contaminant level has not been set, while a guidance value of 6 ppb has been suggested by Health Canada. Perchlorate is measured in environmental samples primarily by ion chromatography. It can be removed from water by anion exchange or membrane filtration. Biological and chemical processes are also effective in removing this species from water.


    Anaerobic biological processes effectively reduce perchlorate to chloride. However, the effluent can be biologically unstable, high in particulates and high in disinfection by-product precursor compounds. Such an effluent would be unsuitable for transmission into a drinking water...

  8. Perchlorate Selectivity of Anion Exchange Resins as Evaluated Using Ion-Selective Electrodes. (United States)

    Yamamoto, Kenji; Mitsuda, Shin'ya; Ohtake, Naomi; Murashige, Natsuki; Ohmuro, Satoshi; Yuchi, Akio


    The selectivity coefficients reported for perchlorate of the high selectivity on anion exchange resins (AXRs) have not been consistent with one another. Possible errors by the unique use of four parameters (concentrations of two anions in two phases) were experimentally verified. The concentrations of perchlorate buffered at low levels (10(-6) - 10(-4) mol L(-1)) by two forms of AXRs were successfully determined by potentiometry with a perchlorate ion-selective electrode. This gave reasonable coefficients. The coefficients for perchlorate on several AXRs were independent of the relative exchange (RE), in contrast to the previous reports. On the other hand, the coefficients for fluoride of the low selectivity that were examined for comparison decreased with an increase in RE, and the dependency was more remarkable for the resins of large exchange capacity.

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

    Energy Technology Data Exchange (ETDEWEB)

    Jama, M.A.; Yuecel, H. (Middle East Technical Univ., Ankara (Turkey))


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

  10. Perchlorate in dust fall and indoor dust in Malta: An effect of fireworks. (United States)

    Vella, Alfred J; Chircop, Cynthia; Micallef, Tamara; Pace, Colette


    We report on the presence of perchlorate in the settleable dust of Malta, a small central Mediterranean island. Both dust fall collected directly as it precipitated from atmosphere over a period of one month and deposited indoor dust from domestic residences were studied. Perchlorate was determined by ion chromatography of water extracts of the collected dusts. Dust fall was collected from 43 towns during 2011 to 2013 and indoor dust was sampled from homes in the same localities. Perchlorate was detected in 108 of 153 samples of dust fall (71%) and in 28 of 37 indoor dust samples (76%). Detectable perchlorate in dust fall ranged from 0.52μgg(-1) to 561μgg(-1) with a median value of 6.2μgg(-1); in indoor dust, levels were from 0.79μgg(-1) to 53μgg(-1) with a median value of 7.8μgg(-1), the highest recorded anywhere to date. Statistical analysis suggested that there was no significant difference in perchlorate content of indoor dust and dust fall. Perchlorate levels in dust fall escalate during the summer in response to numerous religious feasts celebrated with fireworks and perchlorate persists at low μgg(-1) concentrations for several months beyond the summer festive period. In Malta, perchlorate derives exclusively from KClO4, imported for fireworks manufacture. Its residue in dust presents an exposure risk to the population, especially via ingestion by hand to mouth transfer. Our results suggest that wherever intensive burning of fireworks takes place, the environmental impact may be much longer lived than realised, mainly due to re-suspension and deposition of contaminated settled dust in the urban environment.

  11. Possible Detection of Perchlorates by the Sample Analysis at Mars (SAM) Instrument: Comparison with Previous Missions (United States)

    Navarro-Gonzalex, Rafael; Sutter, Brad; Archer, Doug; Ming, Doug; Eigenbrode, Jennifer; Franz, Heather; Glavin, Daniel; McAdam, Amy; Stern, Jennifer; McKay, Christopher; Coll, Patrice; Cabane, Michel; Mahaffy, Paul; Conrad, Pamela; Martin-Torres, Francisco; Zorzano-Mier, Maria; Grotzinger, John


    The first chemical analysis of soluble salts in the soil was carried out by the Phoenix Lander in the Martian Arctic [1]. Surprisingly, chlorine was present as magnesium or calcium perchlorate at 0.4 to 0.6 percent. Additional support for the identification of perchlorate came from the evolved gas analysis which detected the release of molecular oxygen at 350-550C [1]. When Mars-like soils from the Atacama Desert were spiked with magnesium perchlorate (1 percent) and heated using the Viking GC-MS protocol, nearly all the organics were combusted but a small amount was chlorinated, forming chloromethane and dichloromethane [2]. These chlorohydrocarbons were detected by the Viking GC-MS experiments when the Martian soil was analyzed but they were considered to be terrestrial contaminants [3]. Reinterpretation of the Viking results suggests trichloromethane, and chloromethylpropene) detected both by SAM QMS and GC-MS derived from known Earth organic contaminants in the instrument [6]. Calcium perchlorate appears to be the best candidate for evolved O2 in the Rocknest samples at this time but other Cl species (e.g., chlorates) are possible and must be evaluated. The potential detection of perchlorates in Rocknest material adds weight to the argument that both Viking Landers measured signatures of perchlorates. Even if the source of the organic carbon detected is still unknown, the chlorine source was likely Martian. Two mechanisms have been hypothesized for the formation of soil perchlorate: (1) Atmospheric oxidation of chlorine; and (2) UV photooxidation of chlorides catalyzed by mineral catalysts [7]. The presence of soil perchlorates in the Martian surface has important implications for the detection of organics [2], carbonates [8] and nitrates [9] by SAM.

  12. 1-Benzyl-piperazine-1,4-diium bis-(perchlorate) monohydrate. (United States)

    Kaabi, Kamel; El Glaoui, Meher; Jeanneau, Erwann; Rzaigui, Mohamed; Ben Nasr, Cherif


    In the title compound, C(11)H(18)N(2) (2+)·2ClO(4) (-)·H(2)O, one perchlor-ate anion is disordered over two orientations in a 0.66 (3):0.34 (3) ratio. Inter-molecular O-H⋯O, N-H⋯O and C-H⋯O hydrogen bonds link the cations, anions and water mol-ecules into ribbons extending along [100].

  13. Preparation of perlite-based magnesium perchlorate desiccant with colour indicator. (United States)

    Wu, L; He, H


    A new desiccant consisting of magnesium perchlorate, expanded perlite and metal chelate was prepared. The performance tests show that the desiccant is superior to magnesium perchlorate desiccant in dehydration efficiency, absorption capacity for water, flow resistance, color indicator and regeneration. It can reduce the amount of water in gases to approximately 0.7 ppm(v/v). Its applications in gas analysis and purification were investigated.

  14. Evaluation of Potential for Monitored Natural Attenuation of Perchlorate in Groundwater (Indian Head) (United States)


    material. There are a wide variety of microorganisms can degrade perchlorate to chloride and oxygen under oxygen limiting conditions (Coates et al., 1999...anaerobic respiration when oxygen is not present. This metabolic versatility suggests that 2 perchlorate reducing microorganisms will be active...consisted of mottled light to olive brown clay to sandy silts. The clay and sand fractions of the silts varied horizontally and vertically. Fine

  15. Anaerobic treatment of army ammunition production wastewater containing perchlorate and RDX. (United States)

    Atikovic, Emina; Suidan, Makram T; Maloney, Stephen W


    Perchlorate is an oxidizer that has been routinely used in solid rocket motors by the Department of Defense and National Aeronautics and Space Administration. Royal Demolition Explosive (RDX) is a major component of military high explosives and is used in a wide variety of munitions. Perchlorate bearing wastewater typically results from production of solid rocket motors, while RDX is transferred to Army industrial wastewaters during load, assemble and pack operations for new munitions, and hot water or steam washout for disposal and deactivation of old munitions (commonly referred to as demilitarization, or simply demil). Biological degradation in Anaerobic Fluidized Bed Reactors (AFBR), has been shown to be an effective method for the removal of both perchlorate and RDX in contaminated wastewater. The focus of this study was to determine the effectiveness of removal of perchlorate and RDX, individually and when co-mingled, using ethanol as an electron donor under steady state conditions. Three AFBRs were used to assess the effectiveness of this process in treating the wastewater. The performance of the bioreactors was monitored relative to perchlorate, RDX, and chemical oxygen demand removal effectiveness. The experimental results demonstrated that the biodegradation of perchlorate and RDX was more effective in bioreactors receiving the single contaminant than in the bioreactor where both contaminants were fed.

  16. Perchlorate reduction by hydrogen autotrophic bacteria and microbial community analysis using high-throughput sequencing. (United States)

    Wan, Dongjin; Liu, Yongde; Niu, Zhenhua; Xiao, Shuhu; Li, Daorong


    Hydrogen autotrophic reduction of perchlorate have advantages of high removal efficiency and harmless to drinking water. But so far the reported information about the microbial community structure was comparatively limited, changes in the biodiversity and the dominant bacteria during acclimation process required detailed study. In this study, perchlorate-reducing hydrogen autotrophic bacteria were acclimated by hydrogen aeration from activated sludge. For the first time, high-throughput sequencing was applied to analyze changes in biodiversity and the dominant bacteria during acclimation process. The Michaelis-Menten model described the perchlorate reduction kinetics well. Model parameters q(max) and K(s) were 2.521-3.245 (mg ClO4(-)/gVSS h) and 5.44-8.23 (mg/l), respectively. Microbial perchlorate reduction occurred across at pH range 5.0-11.0; removal was highest at pH 9.0. The enriched mixed bacteria could use perchlorate, nitrate and sulfate as electron accepter, and the sequence of preference was: NO3(-) > ClO4(-) > SO4(2-). Compared to the feed culture, biodiversity decreased greatly during acclimation process, the microbial community structure gradually stabilized after 9 acclimation cycles. The Thauera genus related to Rhodocyclales was the dominated perchlorate reducing bacteria (PRB) in the mixed culture.

  17. An improved ion chromatographic method for determination of trace levels of perchlorate in environmental water

    Institute of Scientific and Technical Information of China (English)


    An improved ion chromatographic (IC)method was developed to determine trace levels of perchlorate in environmental water samples.Perchlorate was separated in the hydroxide selective column IonPac AS 16 using NaOH as an eluent with an organic modifier.To eliminate the coelution of perchlorate and 4-chlorobenzene sulfonate (4-CBS),an organic solvent as modifier was added to the eluent.Of four organic solvents studied,acetonitrile proved to be the most efficient based on the retention time of perchlorate and 4-CBS.To improve the method sensitivity,a concentrator column (AGI9) was used to concentrate perchlorate online.With the adoption of a preconcentration step,the sensitivity of our method was improved and the method detection limit (MDL) was reduced to 0.1 μg/L.The linear range was from 0.2 μg/L to 200/.μg/L with a linear correlation coefficient of 0.9989 and the relative standard deviation (RSD) of peak area for eleven successive injections of 0.5 μg/L perehlorate was 4.2%.The method had been applied to the determination of perchlorate in some real environmental water samples and recovery was between 93% and 113%.

  18. Perchlorate contamination of groundwater from fireworks manufacturing area in South India. (United States)

    Isobe, Tomohiko; Ogawa, Shohei P; Sugimoto, Rina; Ramu, Karri; Sudaryanto, Agus; Malarvannan, Govindan; Devanathan, Gnanasekaran; Ramaswamy, Babu Rajendran; Munuswamy, Natesan; Ganesh, Deavaraj Sankar; Sivakumar, Jeyaraj; Sethuraman, A; Parthasarathy, V; Subramanian, Annamalai; Field, Jennifer; Tanabe, Shinsuke


    Perchlorate contamination was investigated in groundwater and surface water from Sivakasi and Madurai in the Tamil Nadu State of South India. Sensitive determination of perchlorate (LOQ = 0.005 μg/L) was achieved by large-volume (500 μL) injection ion chromatography coupled with tandem mass spectrometry. Concentrations of perchlorate were <0.005-7,690 μg/L in groundwater (n = 60), <0.005-30.2 μg/L in surface water (n = 11), and 0.063-0.393 μg/L in tap water (n = 3). Levels in groundwater were significantly higher in the fireworks factory area than in the other locations, indicating that the fireworks and safety match industries are principal sources of perchlorate pollution. This is the first study that reports the contamination status of perchlorate in this area and reveals firework manufacture to be the pollution source. Since perchlorate levels in 17 out of 57 groundwater samples from Sivakasi, and none from Madurai, exceeded the drinking water guideline level proposed by USEPA (15 μg/L), further investigation on human health is warranted.

  19. Effects of ammonium concentration and charge exchange on ammonium recovery from high strength wastewater using a microbial fuel cell

    NARCIS (Netherlands)

    Kuntke, P.; Geleij, M.; Bruning, H.; Zeeman, G.; Hamelers, H.V.M.; Buisman, C.J.N.


    Ammonium recovery using a 2 chamber microbial fuel cell (MFC) was investigated at high ammonium concentration. Increasing the ammonium concentration (from 0.07 g to 4 g ammonium-nitrogen/L) by addition of ammonium chloride did not affect the performance of the MFC. The obtained current densities by

  20. 49 CFR 176.415 - Permit requirements for Division 1.5, ammonium nitrates, and certain ammonium nitrate fertilizers. (United States)


    ... 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...

  1. PERCHLORATE: Occurrence is Widespread but at Varying Levels; Federal Agencies Have Taken Some Actions to Respond to and Lessen Releases (United States)


    tomatoes and spinach, having higher perchlorate levels than others. According to researchers, concentrations of perchlorate at or above 100 parts per...These food items represent the major components of the American diet, such as dairy, meat, fruits, and vegetables. Certain foods, such as tomatoes ...Administration’s Total Diet Study: Dietary intake of perchlorate and iodine ,” Journal of Exposure Science and Environmental Epidemiology, vol. 18 (2008

  2. The nucleation kinetics of ammonium metavanadate precipitated by ammonium chloride (United States)

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


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

  3. Study of microbial perchlorate reduction: Considering of multiple pH, electron acceptors and donors

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Xing [Key Laboratory of Water Pollution Control and Recycling (Shandong), School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Gao, Baoyu, E-mail: [Key Laboratory of Water Pollution Control and Recycling (Shandong), School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Jin, Bo [School of Chemical Engineering, The University of Adelaide, Adelaide SA 5005,Australia (Australia); Zhen, Hu [Key Laboratory of Water Pollution Control and Recycling (Shandong), School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Wang, Xiaoyi [CSIRO Land and Water, Gate 5, Waite Road, Urrbrae, SA 5064 (Australia); Dai, Ming [School of Chemical Engineering, The University of Adelaide, Adelaide SA 5005,Australia (Australia)


    Graphical abstract: Schemes of perchlorate reduction in ClO{sub 4}{sup −}/ClO{sub 3}{sup −}–NO{sub 3}{sup −} e{sup −}acceptor systems. - Highlights: • We created a multiple electron acceptor/donor system for ClO{sub 4}{sup −} reduction. • Nitrate reduction was inhibited when using perchlorate-grown Azospira sp. KJ. • Reduction proceeded as an order of ClO{sub 3}{sup −}, ClO{sub 4}{sup −}and NO{sub 3}{sup −}. • Oxidation of acetate was inhibited by succinate in acetate–succinate series. - Abstract: Bioremediation of perchlorate-cotaminated water by a heterotrophic perchlorate reducing bacterium creates a multiple electron acceptor-donor system. We experimentally determined the perchlorate reduction by Azospira sp. KJ at multiple pH, electron acceptors and donors systems; this was the aim of this study. Perchlorate reduction was drastically inhibited at the pH 6.0, and the maximum reduction of perchlorate by Azospira sp. KJ was observed at pH value of 8.0. Perchlorate reduction was retarded in ClO{sub 4}{sup −}–ClO{sub 3}{sup −}, ClO{sub 4}{sup −}–ClO{sub 3}{sup −}–NO{sub 3}{sup −},and ClO{sub 4}{sup −}–NO{sub 3}{sup −} acceptor systems, while being completely inhibited by the additional O{sub 2} in the ClO{sub 4}{sup −}–O{sub 2} acceptor system. The reduction proceeded as an order of ClO{sub 3}{sup −}, ClO{sub 4}{sup −}, and NO{sub 3}{sup −} in the ClO{sub 4}{sup −}–ClO{sub 3}{sup −}–NO{sub 3}{sup −} system. K{sub S,}v{sub max}, and q{sub max} obtained at different e{sup −} acceptor and donor conditions are calculated as 140.5–190.6 mg/L, 8.7–13.2 mg-perchlorate/L-h, and 0.094–0.16 mg-perchlorate/mg-DW-h, respectively.

  4. Ammonium sulfate preparation from phosphogypsum waste

    Directory of Open Access Journals (Sweden)

    Abdel-Hakim T. Kandil


    Full Text Available The Egyptian phosphogypsum waste is treated using sulfuric acid prior the ammonium sulfate production. The relevant factors that would affect the removal efficiencies of some impurities are studied. The optimum conditions of the treatment are 8 M sulfuric acid solution and 1/4 solid/liquid ratio for 30 min contact time at 80 °C. Moreover, the optimum conditions of the ammonium sulfate preparation are 10 g of the suspended impure or purified phosphogypsum in 40 ml of 3% ammonium sulfate solution (as initiator, 1/4 solid/liquid ratio at pH7 at an addition of an excess ammonium carbonate, and 150 rpm stirring speed for 4.0 h contact time at 55 °C as well as the 5 mg of barium chloride is added to remove the radium in the ammonium sulfate product. Finally, the ammonium sulfate is crystallized and the chemical analysis of the product shows 20% nitrogen and 23.6% sulfur. Therefore, the purity of the obtained ammonium sulfate is 95% from the purified phosphogypsum.

  5. Substrate specificity of Rhbg: ammonium and methyl ammonium transport. (United States)

    Nakhoul, Nazih L; Abdulnour-Nakhoul, Solange M; Boulpaep, Emile L; Rabon, Edd; Schmidt, Eric; Hamm, L Lee


    Rhbg is a nonerythroid membrane glycoprotein belonging to the Rh antigen family. In the kidney, Rhbg is expressed at the basolateral membrane of intercalated cells of the distal nephron and is involved in NH4+ transport. We investigated the substrate specificity of Rhbg by comparing transport of NH3/NH4+ with that of methyl amine (hydrochloride) (MA/MA+), often used to replace NH3/NH4+, in oocytes expressing Rhbg. Methyl amine (HCl) in solution exists as neutral methyl amine (MA) in equilibrium with the protonated methyl ammonium (MA+). To assess transport, we used ion-selective microelectrodes and voltage-clamp experiments to measure NH3/NH4+- and MA/MA+-induced intracellular pH (pH(i)) changes and whole cell currents. Our data showed that in Rhbg oocytes, NH3/NH4+ caused an inward current and decrease in pH(i) consistent with electrogenic NH4+ transport. These changes were significantly larger than in H2O-injected oocytes. The NH3/NH4+-induced current was not inhibited in the presence of barium or in the absence of Na+. In Rhbg oocytes, MA/MA+ caused an inward current but an increase (rather than a decrease) in pH(i). MA/MA+ did not cause any changes in H2O-injected oocytes. The MA/MA+-induced current and pH(i) increase were saturated at higher concentrations of MA/MA+. Amiloride inhibited MA/MA+-induced current and the increase in pH(i) in oocytes expressing Rhbg but had no effect on control oocytes. These results indicate that MA/MA+ is transported by Rhbg but differently than NH3/NH4+. The protonated MA+ is likely a direct substrate whose transport resembles that of NH4+. Transport of electroneutral MA is also enhanced by expression of Rhbg.

  6. Effect of perchlorate in fertilisers on lettuce and fruit vegetables : Uptake and distribution of perchlorate in greenhouse soil-grown butterhead lettuce and solless-grown cucumber, sweet pepper, round and cherry tomate

    NARCIS (Netherlands)

    Voogt, W.; Eveleens, B.A.; Steenhuizen, J.W.; Vandevelde, I.; Vis, de R.; Lommel, van J.


    In 2013 traces of perchlorate were detected in fruits and vegetable samples. Because perchlorate (ClO4 -) is part of a group of substances (goitrogens) that may inhibit the uptake of iodine by the thyroid, these findings caused commotion in the markets. Fertilizers were named as one of the sources o

  7. Chlorine-36 abundance in natural and synthetic perchlorate

    Energy Technology Data Exchange (ETDEWEB)

    Heikoop, Jeffrey M [Los Alamos National Laboratory; Dale, M [NON LANL; Sturchio, Neil C [UNIV OF ILLIONOIS; Caffee, M [PURDUE UNIV; Belosa, A D [UNIV OF ILLINOIS; Heraty, Jr., L J [UNIV OF ILLINOIS; Bohike, J K [RESTON, VA; Hatzinger, P B [SHAW ENIVIORNMENTAL C0.; Jackson, W A [TEXAS TECH; Gu, B [ORNL


    Perchlorate (ClO{sub 4}{sup -}) is ubiquitous in the environment. It occurs naturally as a product of atmospheric photochemical reactions, and is synthesized for military, aerospace, and industrial applications. Nitrate-enriched soils of the Atacama Desert (Chile) contain high concentrations of natural ClO{sub 4}{sup -}; nitrate produced from these soils has been exported worldwide since the mid-1800's for use in agriculture. The widespread introduction of synthetic and agricultural ClO{sub 4}{sup -} into the environment has complicated attempts to understand the geochemical cycle of ClO{sub 4}{sup -}. Natural ClO{sub 4}{sup -} samples from the southwestern United States have relatively high {sup 36}Cl abundances ({sup 36}Cl/Cl = 3,100 x 10{sup -15} to 28,800 x 10{sup -15}), compared with samples of synthetic ({sup 36}Cl/Cl = 0.0 x 10{sup -15} to 40 x 10{sup -15}) and Atacama Desert ({sup 36}Cl/Cl = 0.9 x 10{sup -15} to 590 x 10{sup -15}) ClO{sub 4}{sup -}. These data give a lower limit for the initial {sup 36}Cl abundance of natural ClO{sub 4}{sup -} and provide temporal and other constraints on its geochemical cycle.

  8. Hydrogen oxidation on gold electrode in perchloric acid solution

    Energy Technology Data Exchange (ETDEWEB)

    Sustersic, M.G.; Almeida, N.V.; Von Mengershausen, A.E. [Facultad de Ingenieria y Ciencias Economico Sociales, Universidad Nacional de San Luis, 25 de Mayo N 384, 5730 Villa Mercedes, San Luis (Argentina)


    The aim of this research is to study the interface gold/perchloric acid solution in presence of hydrogen. The reactive is generated by H{sup +} ion reduction and by saturating the electrolyte with the gaseous H{sub 2}. No evidence of H{sub 2} dissociative adsorption is found. In special conditions, a strongly adsorbed layer is formed from the atoms diffusing from inside of the metal. The mass transport occurs in three ways: the diffusion of H atoms inwards, the diffusion of H atoms back to the surface and the dissolved H{sub 2} diffusion from the bulk electrolyte to the surface. When dissolved H{sub 2} reacts, the reaction is kinetically controlled when the H{sub 2} partial pressure is high, and it is diffusionally controlled when the reactive partial pressure is low. Above 0.7 V, (measured vs. RHE), the (100) plane surface reconstruction lifts, and the rate determining step is the H diffusion towards inside of the metal, and the current suddenly falls. The Hydrogen redox reaction on gold shows reversibility with respect to the potential when the reactives are the H diffusing outwards of the metal and the H{sup +} ion present in the electrolyte. However, the absolute current values of oxidation and reduction are different because the reactive sources are different. (author)

  9. Effects of lanthanum nitrate on growth and chlorophyll fluorescence characteristics of Alternanthera philoxeroides under perchlorate stress

    Institute of Scientific and Technical Information of China (English)

    谢寅峰; 蔡贤雷; 刘伟龙; 陶功胜; 陈倩; 张强


    To investigate the effects of exogenous lanthanum (La) on Alternanthera philoxeroides (Mart.) Griseb under perchlorate stress, changes in the growth and physiological parameters were investigated in solution culture experiments under controlled condi-tions. Different concentrations of La (NO3)3 were used in our study. It was shown that 0.1 and 0.5 mg/L La3+alleviated the inhibition effect of perchlorate on A. philoxeroides, including relative growth yield, dry weight of different organs, leaf area and root activity. And La3+prevented decline in the relative chlorophyll content and chlorophyll fluorescence parameters including Fv/Fm, Fv'/Fm',ΦPSI and ETR induced by perchlorate stress. Moreover, 0.5 mg/L La3+showed an optimal mitigative effect, while excess La3+(5.0 mg/L) led to synergistic effect on stress. Correlation analysis revealed a significant positive relationship between growth indexes and the chlorophyll fluorescence parameters, root activity and relative chlorophyll content (p<0.05). The results suggested that appropriate concentration of La3+could effectively alleviate growth inhibition and injury of A. philoxeroides caused by perchlorate stress, and the mitigative effect of La3+might be achieved by improving root activity, maintaining chlorophyll content and promoting photochemical efficiency of photosystem II of A. philoxeroides under perchlorate stress.

  10. Possible Calcite and Magnesium Perchlorate Interaction in the Mars Phoenix Thermal and Evolved Gas Analyzer (TEGA) (United States)

    Cannon, K. M.; Sutter, B.; Ming, D. W.; Boynton, W. V.; Quinn, R. C.


    The Mars Phoenix Lander's TEGA instrument detected a calcium carbonate phase decomposing at high temperatures (approx.700 C) from the Wicked Witch soil sample [1]. TEGA also detected a lower temperature CO2 release between 400 C and 680 C [1]. Possible explanations given for this lower temperature CO2 release include thermal decomposition of Mg or Fe carbonates, a zeolitictype desorption reaction, or combustion of organic compounds in the soil [2]. The detection of 0.6 wt % soluble perchlorate by the Wet Chemistry Laboratory (WCL) on Phoenix [3] has implications for the possibility of organic molecules in the soil. Ming et al. [4] demonstrated that perchlorates could have oxidized organic compounds to CO2 in TEGA, preventing detection of their characteristic mass fragments. Here, we propose that a perchlorate salt and calcium carbonate present in martian soil reacted to produce the 400 C - 680 C TEGA CO2 release. The parent salts of the perchlorate on Mars are unknown, but geochemical models using WCL data support the possible dominance of Mg-perchlorate salts [5]. Mg(ClO4)2 6H2O is the stable phase at ambient martian conditions [6], and breaks down at lower temperatures than carbonates giving off Cl2 and HCl gas [7,8]. Devlin and Herley [7] report two exotherms at 410-478 C and 473-533 C which correspond to the decomposition of Mg(ClO4)2.

  11. [Determination of iodide, thiocyanate and perchlorate ions in environmental water by two-dimensional ion chromatography]. (United States)

    Lin, Li; Wang, Haibo; Shi, Yali


    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%.

  12. Highly Selective Perchlorate Membrane Electrode Based on Cobalt(Ⅲ) Schiff Base as a Neutral Carrier

    Institute of Scientific and Technical Information of China (English)

    SHOKROLLAHI Ardeshir; GHAEDI Mehrorang; RAJABI, Harold Reza; KIANFAR, Ali Hossein


    A highly selective poly(vinyl chloride) (PVC) membrane electrode based on Co(Ⅲ)-Schiff base [Co(5-NO2-Salen)(PBu3)]ClO4·H2O (where 5-NO2-SalenH=bis(5-nitrosalycilaldehyde)ethylenediamine) as a new carrier for construction of perchlorate-selective electrode by incorporating the membrane ingredients on the surface of a graphite electrodes has been reported. The proposed electrode possesses a very wide Nernestian potential linear range to perchlorate from 1.0×10-6 to 5.0×10-1 mol·L-1 with a slope of (59.4±0.9) mV per decade of perchlo-rate concentration with a low detection limit of 5.0×10-7 mol·L-1 and good perchlorate selectivity over the wide variety of other anions. The developed electrode has an especially fast response (<5 s) and a wide pH independent range (3.0-12.0) in comparison with recent reported electrodes and can be used for at least 2 months without any considerable divergence in their potential response. This electrode was used for the determination of perchlorate in river water, drinking water, sludgy water and human urine with satisfactory results without complicated and time consuming pretreatment.

  13. Occurrence of perchlorate in drinking water and seawater in South Korea. (United States)

    Her, Namguk; Jeong, Hyunchan; Kim, Jongsung; Yoon, Yeomin


    Concentrations of perchlorate were determined by both liquid-chromatography-mass spectrometry (LC-MS) and ion chromatography tandem mass spectrometry (IC-MS/MS) in 520 tap-water, 48 bottled-water, and 9 seawater samples obtained or purchased from >100 different locations in South Korea. The method detection limits were 0.013 μg/L for LC-MS and 0.005 μg/L for IC-MS/MS, and the limits of quantification (LOQs) were 0.10 μg/L for LC-MS and 0.032 μg/L for IC-MS/MS. Perchlorate was detected in most (80%) of the tap-water samples, with concentrations higher than the LOQ; the concentrations ranged from water samples, with concentrations higher then the LOQ, ranging from 0.04 to 0.29 μg/L (mean 0.07 ± 0.01). The concentrations of perchlorate in all seawater samples collected from the various locations were higher than the LOQ, with a mean concentration of 1.15 ± 0.01 μg/L (maximum 6.11 and minimum 0.11). This study provides further evidence that drinking-water sources have been contaminated by perchlorate. To the best of our knowledge, this is the first comprehensive study on perchlorate assessment in drinking water and seawater in South Korea.

  14. Perchlorate and Nitrate Remediation Efficiency and Microbial Diversity in a Containerized Wetland Bioreactor

    Energy Technology Data Exchange (ETDEWEB)

    Jr., B D; Dibley, V; Pinkart, H; Legler, T


    We have developed a method to remove perchlorate (14 to 27 {micro}g/L) and nitrate (48 mg/L) from contaminated groundwater using a wetland bioreactor. The bioreactor has operated continuously in a remote field location for more than two years with a stable ecosystem of indigenous organisms. This study assesses the bioreactor for long-term perchlorate and nitrate remediation by evaluating influent and effluent groundwater for reduction-oxidation conditions and nitrate and perchlorate concentrations. Total community DNA was extracted and purified from 10-g sediment samples retrieved from vertical coring of the bioreactor during winter. Analysis by denaturing gradient gel electrophoresis of short, 16S rDNA, polymerase-chain-reaction products was used to identify dominant microorganisms. Bacteria genera identified were closely affiliated with bacteria widely distributed in soils, mud layers, and fresh water. Of the 17 dominant bands sequenced, most were gram negative and capable of aerobic or anaerobic respiration with nitrate as the terminal electron acceptor (Pseudomonas, Acinetobacter, Halomonas, and Nitrospira). Several identified genera (Rhizobium, Acinetobactor, and Xanthomonas) are capable of fixing atmospheric nitrogen into a combined form (ammonia) usable by host plants. Isolates were identified from the Proteobacteria class, known for the ability to reduce perchlorate. Initial bacterial assessments of sediments confirm the prevalence of facultative anaerobic bacteria capable of reducing perchlorate and nitrate in situ.


    Perchlorate has been identified in ground and surface waters around the US, including some that serve as supplies for drinking water. Because perchlorate salts are used as solid oxidants in rockets and ordnance, water contamination may occur near military or aerospace installatio...

  16. Kinetics of nitrate and perchlorate reduction in ion exchange brine using the membrane biofilm reactor (MBfR) (United States)

    Several sources of bacterial inocula were tested for their ability to reduce nitrate and perchlorate in synthetic ion-exchange spent brine (3-4.5% salinity) using a hydrogen-based membrane biofilm reactor (MBfR). Nitrate and perchlorate removal fluxes reached as high as 5.4 g N ...

  17. 77 FR 65532 - Solid Fertilizer Grade Ammonium Nitrate From the Russian Federation: Notice of Rescission of... (United States)


    ... 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... Administrative Review: Solid Fertilizer Grade Ammonium Nitrate (Ammonium Nitrate) from the Russian...

  18. A simplified method for obtaining high-purity perchlorate from groundwater for isotope analyses.

    Energy Technology Data Exchange (ETDEWEB)

    vonKiparski, G; Hillegonds, D


    Investigations into the occurrence and origin of perchlorate (ClO{sub 4}{sup -}) found in groundwater from across North America have been sparse until recent years, and there is mounting evidence that natural formation mechanisms are important. New opportunities for identifying groundwater perchlorate and its origin have arisen with the utilization of improved detection methods and sampling techniques. Additionally, application of the forensic potential of isotopic measurements has begun to elucidate sources, potential formation mechanisms and natural attenuation processes. Procedures developed appear to be amenable to enable high precision stable isotopic analyses, as well as lower precision AMS analyses of {sup 36}Cl. Immediate work is in analyzing perchlorate isotope standards and developing full analytical accuracy and uncertainty expectations. Field samples have also been collected, and will be analyzed when final qa/qc samples are deemed acceptable.

  19. Microbial perchlorate reduction: A precise laboratory determination of the chlorine isotope fractionation and its possible biochemical basis (United States)

    Ader, Magali; Chaudhuri, Swades; Coates, John D.; Coleman, Max


    Perchlorate-reducing bacteria fractionate chlorine stable isotopes giving a powerful approach to monitor the extent of microbial consumption of perchlorate in contaminated sites undergoing remediation or natural perchlorate containing sites. This study reports the full experimental data and methodology used to re-evaluate the chlorine isotope fractionation of perchlorate reduction in duplicate culture experiments of Azospira suillum strain PS at 37 °C (Δ 37Cl Cl --ClO 4-) previously reported, without a supporting data set by Coleman et al. [Coleman, M.L., Ader, M., Chaudhuri, S., Coates, J.D., 2003. Microbial Isotopic Fractionation of Perchlorate Chlorine. Appl. Environ. Microbiol. 69, 4997-5000] in a reconnaissance study, with the goal of increasing the accuracy and precision of the isotopic fractionation determination. The method fully described here for the first time, allows the determination of a higher precision Δ 37Cl Cl --ClO 4- value, either from accumulated chloride content and isotopic composition or from the residual perchlorate content and isotopic composition. The result sets agree perfectly, within error, giving average Δ 37Cl Cl --ClO 4- = - 14.94 ± 0.15‰. Complementary use of chloride and perchlorate data allowed the identification and rejection of poor quality data by applying mass and isotopic balance checks. This precise Δ 37Cl Cl --ClO 4- value can serve as a reference point for comparison with future in situ or microcosm studies but we also note its similarity to the theoretical equilibrium isotopic fractionation between a hypothetical chlorine species of redox state + 6 and perchlorate at 37 °C and suggest that the first electron transfer during perchlorate reduction may occur at isotopic equilibrium between an enzyme-bound chlorine and perchlorate.

  20. Effects of larval-juvenile treatment with perchlorate and co-treatment with thyroxine on zebrafish sex ratios (United States)

    Mukhi, S.; Torres, L.; Patino, R.


    The objective of this study was to determine the effect of larval-juvenile exposure to perchlorate, a thyroid hormone synthesis inhibitor, on the establishment of gonadal sex ratios in zebrafish. Zebrafish were exposed to untreated water or water containing perchlorate at 100 or 250 ppm for a period of 30 days starting at 3 days postfertilization (dpf). Recovery treatments consisted of a combination of perchlorate and exogenous thyroxine (T4; 10 nM). Thyroid histology was assessed at the end of the treatment period (33 dpf), and gonadal histology and sex ratios were determined in fish that were allowed an additional 10-day period of growth in untreated water. As expected, exposure to perchlorate caused changes in thyroid histology consistent with hypothyroidism and these effects were reversed by co-treatment with exogenous T4. Perchlorate did not affect fish survival but co-treatment with T4 induced higher mortality. However, relative to the corresponding perchlorate concentration, co-treatment with T4 caused increased mortality only at a perchlorate concentration of 100 ppm. Perchlorate alone or in the presence of T4 suppressed body length at 43 dpf relative to control values. Perchlorate exposure skewed the sex ratio toward female in a concentration-dependent manner, and co-treatment with T4 not only blocked the feminizing effect of perchlorate but also overcompensated by skewing the sex ratio towards male. Moreover, co-treatment with T4 advanced the onset of spermatogenesis in males. There was no clear association between sex ratios and larval survival or growth. We conclude that endogenous thyroid hormone plays a role in the establishment of gonadal sex phenotype during early development in zebrafish. ?? 2006 Elsevier Inc. All rights reserved.

  1. Effects of prolonged exposure to perchlorate on thyroid and reproductive function in zebrafish (United States)

    Mukhi, S.; Patino, R.


    The objectives of this study were to determine the effects of prolonged exposure to perchlorate on (1) thyroid status and reproductive performance of adult zebrafish (Danio rerio) and (2) F1 embryo survival and early larval development. Using a static-renewal procedure, mixed sex populations of adult zebrafish were exposed to 0, 10, and 100 mg/l nominal concentrations of waterborne perchlorate for 10 weeks. Thyroid histology was qualitatively assessed, and females and males were separated and further exposed to their respective treatments for six additional weeks. Eight females in each tank replicate (n = 3) were paired weekly with four males from the same respective treatment, and packed-egg (spawn) volume (PEV) was measured each of the last five weeks. At least once during weeks 14-16 of exposure, other end points measured included fertilization rate, fertilized egg diameter, hatching rate, standard length, and craniofacial development of 4-day-postfertilization larvae and thyroid hormone content of 3.5-h embryos and of exposed mothers. At 10 weeks of exposure, perchlorate at both concentrations caused thyroidal hypertrophy and colloid depletion. A marked reduction in PEV was observed toward the end of the 6-week spawning period, but fertilization and embryo hatching rates were unaffected. Fertilized egg diameter and larval length were increased by parental exposure to perchlorate. Larval head depth was unaffected but the forward protrusion of the lower jaw-associated cartilage complexes, Meckel's and ceratohyal, was decreased. Exposure to both concentrations of perchlorate inhibited whole-body thyroxine content in mothers and embryos, but triiodothyronine content was unchanged. In conclusion, prolonged exposure of adult zebrafish to perchlorate not only disrupts their thyroid endocrine system but also impairs reproduction and influences early F1 development. ?? 2007 Oxford University Press.

  2. Fractionation of stable isotopes in perchlorate and nitrate during in situ biodegradation in a sandy aquifer (United States)

    Bohlke, Johnkarl F.; Hatzinger, P.B.; Sturchio, N.C.; Gu, B.; Heraty, L.J.; Borden, R.C.


    An in situ experiment was performed in a shallow alluvial aquifer in Maryland to quantify the fractionation of stable isotopes in perchlorate (Cl and O) and nitrate (N and O) during biodegradation. An emulsified soybean oil substrate that was previously injected into this aquifer provided the electron donor necessary for biological perchlorate reduction and denitrification. During the field experiment, groundwater extracted from an upgradient well was pumped into an injection well located within the in situ oil barrier, and then groundwater samples were withdrawn for the next 30 h. After correction for dilution (using Br– as a conservative tracer of the injectate), perchlorate concentrations decreased by 78% and nitrate concentrations decreased by 82% during the initial 8.6 h after the injection. The observed ratio of fractionation effects of O and Cl isotopes in perchlorate (e18O/e37Cl) was 2.6, which is similar to that observed in the laboratory using pure cultures (2.5). Denitrification by indigenous bacteria fractionated O and N isotopes in nitrate at a ratio of ~0.8 (e18O/e15N), which is within the range of values reported previously for denitrification. However, the magnitudes of the individual apparent in situ isotope fractionation effects for perchlorate and nitrate were appreciably smaller than those reported in homogeneous closed systems (0.2 to 0.6 times), even after adjustment for dilution. These results indicate that (1) isotope fractionation factor ratios (e18O/e37Cl, e18O/e15N) derived from homogeneous laboratory systems (e.g. pure culture studies) can be used qualitatively to confirm the occurrence of in situ biodegradation of both perchlorate and nitrate, but (2) the magnitudes of the individual apparent e values cannot be used quantitatively to estimate the in situ extent of biodegradation of either anion.

  3. Contact Electrification of Regolith Particles and Chloride Electrolysis: Synthesis of Perchlorates on Mars (United States)

    Tennakone, K.


    Contact electrification of chloride-impregnated martian regolith particles due to eolian agitation and moisture condensation on coalesced oppositely charged grains may lead to spontaneous electrolysis that generates hypochlorite, chlorite, chlorate, and perchlorate with a concomitant reduction of water to hydrogen. This process is not curtailed even if moisture condenses as ice because chloride ionizes on the surface of ice. Limitations dictated by potentials needed for electrolysis and breakdown electric fields enable estimation of the required regolith grain size. The estimated dimension turns out to be of the same order of magnitude as the expected median size of martian regolith, and a simple calculation yields the optimum rate of perchlorate production.

  4. Linking methane oxidation with perchlorate reduction: a microbial base for possible Martian life (United States)

    Miller, L. G.; Carlstrom, C.; Baesman, S. M.; Coates, J. D.; Oremland, R. S.


    Recent observations of methane (CH4) and perchlorate (ClO4-) within the atmosphere and surface of Mars, respectively, provide impetus for establishing a metabolic linkage between these compounds whereby CH4 acts as an electron donor and perchlorate acts as an electron acceptor. Direct linkage through anaerobic oxidation of methane (AOM) has not been observed. However, indirect syntrophic oxygenase-dependent oxidation of CH4 with an aerobic methane oxidizer is feasible. The pathway for anaerobic dissimilatory perchlorate reduction includes 3 steps. The first 2 are sequential reductions of (1) perchlorate to chlorate and (2) chlorate to chlorite, mediated by perchlorate reductase. The third step is disproportionation of chlorite to chloride and molecular oxygen, mediated by chlorite dismutase. Utilization of thusly derived oxygen by hydrocarbon-degrading organisms in anoxic environments was first demonstrated by Coates et. al. (1998)1, however the link to aerobic methane oxidation was not examined at that time. Here, we systematically explore the potential for several species of aerobic methanotrophs to couple with chlorite during dissimilatory perchlorate reduction. In one experiment, 0.5 kPa CH4 was completely removed in one day from the headspace of combined cell suspensions of Dechloromonas agitata strain CKB and Methylococcus capsulatus in the presence of 5 mM chlorite. Oxidation of labeled 14CH4 to 14CO2 under similar conditions was later confirmed. Another experiment demonstrated complete removal of 0.2 kPa CH4 over several days by Methylobacter albus strain BG8 with strain CKB in the presence of 5 mM chlorite. Finally, we observed complete removal of 0.2 kPa CH4 in bottles containing natural soil (enriched in methanotrophs by CH4 additions over several weeks) and strain CKB and in the presence of 10 mM chlorite. This soil, collected from a pristine lake shoreline, demonstrated endogenous methane, perchlorate, chlorate and chlorite uptake. Other soil and

  5. Perchlorate in Lake Water from an Operating Diamond Mine. (United States)

    Smith, Lianna J D; Ptacek, Carol J; Blowes, David W; Groza, Laura G; Moncur, Michael C


    Mining-related perchlorate [ClO4(-)] in the receiving environment was investigated at the operating open-pit and underground Diavik diamond mine, Northwest Territories, Canada. Samples were collected over four years and ClO4(-) was measured in various mine waters, the 560 km(2) ultraoligotrophic receiving lake, background lake water and snow distal from the mine. Groundwaters from the underground mine had variable ClO4(-) concentrations, up to 157 μg L(-1), and were typically an order of magnitude higher than concentrations in combined mine waters prior to treatment and discharge to the lake. Snow core samples had a mean ClO4(-) concentration of 0.021 μg L(-1) (n=16). Snow and lake water Cl(-)/ClO4(-) ratios suggest evapoconcentration was not an important process affecting lake ClO4(-) concentrations. The multiyear mean ClO4(-) concentrations in the lake were 0.30 μg L(-1) (n = 114) in open water and 0.24 μg L(-1) (n = 107) under ice, much below the Canadian drinking water guideline of 6 μg L(-1). Receiving lake concentrations of ClO4(-) generally decreased year over year and ClO4(-) was not likely [biogeo]chemically attenuated within the receiving lake. The discharge of treated mine water was shown to contribute mining-related ClO4(-) to the lake and the low concentrations after 12 years of mining were attributed to the large volume of the receiving lake.

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

    Institute of Scientific and Technical Information of China (English)



    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.

  7. Calcium sulphate in ammonium sulphate solution (United States)

    Sullivan, E.C.


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

  8. Reduction in Ammonium Ions in Sludge Liquor

    Directory of Open Access Journals (Sweden)

    Eglė Šlajūtė


    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

  9. On the evaporation of ammonium sulfate solution

    Energy Technology Data Exchange (ETDEWEB)

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


    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.

  10. Kinetics of nitrate and perchlorate reduction in ion-exchange brine using the membrane biofilm reactor (MBfR). (United States)

    Van Ginkel, Steven W; Ahn, Chang Hoon; Badruzzaman, Mohammad; Roberts, Deborah J; Lehman, S Geno; Adham, Samer S; Rittmann, Bruce E


    Several sources of bacterial inocula were tested for their ability to reduce nitrate and perchlorate in synthetic ion-exchange spent brine (30-45 g/L) using a hydrogen-based membrane biofilm reactor (MBfR). Nitrate and perchlorate removal fluxes reached as high as 5.4 g Nm(-2)d(-1) and 5.0 g ClO(4)m(-2)d(-1), respectively, and these values are similar to values obtained with freshwater MBfRs. Nitrate and perchlorate removal fluxes decreased with increasing salinity. The nitrate fluxes were roughly first order in H(2) pressure, but roughly zero-order with nitrate concentration. Perchlorate reduction rates were higher with lower nitrate loadings, compared to high nitrate loadings; this is a sign of competition for H(2). Nitrate and perchlorate reduction rates depended strongly on the inoculum. An inoculum that was well acclimated (years) to nitrate and perchlorate gave markedly faster removal kinetics than cultures that were acclimated for only a few months. These results underscore that the most successful MBfR bioreduction of nitrate and perchlorate in ion-exchange brine demands a well-acclimated inoculum and sufficient hydrogen availability.

  11. Systematics of Natural Perchlorate in Precipitation, Soils, and Plants at the Amargosa Desert Research Site, Nye County, Nevada (United States)

    Andraski, B. J.; Stonestrom, D. A.; Jackson, W. A.; Rajagopalan, S.; Taylor, E. M.


    Naturally occurring perchlorate is known to be associated with nitrate deposits of the hyperarid Atacama Desert in Chile, and recent large-scale sampling has identified a substantial reservoir (up to 1 kg/ha) of natural perchlorate in diverse unsaturated zones of the arid and semiarid Southwestern United States (Rao et al., 2007, ES&T, DOI: 10.1021/es062853i). The objective of the Amargosa Desert work is to develop a better understanding of the deposition, accumulation, and biological cycling of perchlorate in arid environments. Occurrence of perchlorate was evaluated by sampling shallow soil profiles up to 3 m in depth at four different locations and at two different time periods, and by sampling dominant plant species growing near the subsurface profiles. Deposition of perchlorate was evaluated by analyzing both bulk deposition (precipitation plus dry fall, collected under oil) collected on site and wet deposition samples collected by the National Atmospheric Deposition program at a nearby site. Soil samples and atmospheric-deposition samples were tested for both perchlorate (ClO4- ) and major anions. Perchlorate concentrations (0.2-20 µg/kg) were variable with depth in soil profiles and generally correlated most highly with chloride (Cl-) and nitrate (NO3-), although the intensity of these relations differed among profiles. Plant concentrations were generally above 1 mg/kg, suggesting ClO4- accumulation. Concentrations of ClO4- were generally much greater in total deposition than wet deposition samples, indicating a substantial dryfall component of meteoric deposition. This presentation will present the mass distribution and variability of perchlorate in bulk deposition, soils, and plants. Reasons for observed relations between subsurface concentrations of perchlorate and other anions will be explored.

  12. (Per)chlorate reduction by an acetogenic bacterium, Sporomusa sp., isolated from an underground gas storage.

    KAUST Repository

    Balk, Melike


    A mesophilic bacterium, strain An4, was isolated from an underground gas storage reservoir with methanol as substrate and perchlorate as electron acceptor. Cells were Gram-negative, spore-forming, straight to curved rods, 0.5-0.8 microm in diameter, and 2-8 microm in length, growing as single cells or in pairs. The cells grew optimally at 37 degrees C, and the pH optimum was around 7. Strain An4 converted various alcohols, organic acids, fructose, acetoin, and H(2)/CO(2) to acetate, usually as the only product. Succinate was decarboxylated to propionate. The isolate was able to respire with (per)chlorate, nitrate, and CO(2). The G+C content of the DNA was 42.6 mol%. Based on the 16S rRNA gene sequence analysis, strain An4 was most closely related to Sporomusa ovata (98% similarity). The bacterium reduced perchlorate and chlorate completely to chloride. Key enzymes, perchlorate reductase and chlorite dismutase, were detected in cell-free extracts.


    A solid fertilizer sample is dissolved or leached to solutilize the perchlorate as the aqueous anion. If needed, the liquid is filtered or centrifuged. The rsulting solution is subjected to ion chromatography using an adaptation of EPA Method 314.0. Preliminary screenng is requir...

  14. A screened hybrid density functional study on energetic complexes: cobalt, nickel and copper carbohydrazide perchlorates. (United States)

    Huang, Huisheng; Zhang, Tonglai; Zhang, Jianguo; Wang, Liqiong


    The molecular geometry, electronic structure, infrared spectra and thermochemical properties of cobalt and nickel tris(carbohydrazide) perchlorates (CoCP and NiCP) as well as copper bis(carbohydrazide) perchlorate (CuCP) were investigated using the Heyd-Scuseria-Ernzerhof (HSE) screened hybrid density functional. The results show that both perchlorate ions coordinate with the copper atom, and the interactions between copper and perchlorate are ionic, whereas all the metal-carbohydrazide interactions are covalent. Due to the delocalization from the sigma(N-H) bond orbital to the n*(M) antibond orbital, the amino stretching vibrations of these complexes show considerable red-shift compared with those of free carbohydrazide ligand. The calculated heats of reaction and formation indicate that the formations of these complexes are exothermic, and the order of their thermal stability is NiCP>CoCP>CuCP. These agree well with the experimental results. Finally, we find that there is a relationship between the energy gap and impact sensitivity.

  15. Heterotrophic-autotrophic sequential system for reductive nitrate and perchlorate removal. (United States)

    Ucar, Deniz; Cokgor, Emine Ubay; Sahinkaya, Erkan


    Nitrate and perchlorate were identified as significant water contaminants all over the world. This study aims at evaluating the performances of the heterotrophic-autotrophic sequential denitrification process for reductive nitrate and perchlorate removal from drinking water. The reduced nitrate concentration in the heterotrophic reactor increased with increasing methanol concentrations and the remaining nitrate/nitrite was further removed in the following autotrophic denitrifying process. The performances of the sequential process were studied under varying nitrate loads of [Formula: see text] at a fixed hydraulic retention time of 2 h. The C/N ratio in the heterotrophic reactor varied between 1.24 and 2.77 throughout the study. Nitrate and perchlorate reduced completely with maximum initial concentrations of [Formula: see text] and 1000 µg/L, respectively. The maximum denitrification rate for the heterotrophic reactor was [Formula: see text] when the bioreactor was fed with [Formula: see text] and 277 mg/L methanol. For the autotrophic reactor, the highest denitrification rate was [Formula: see text] in the first period when the heterotrophic reactor performance was low. Perchlorate reduction was initiated in the heterotrophic reactor, but completed in the following autotrophic process. Effluent sulphate concentration was below the drinking water standard level of 250 mg/L and pH was in the neutral level.

  16. Double-Polymer-Modified Pencil Lead for Stripping Voltammetry of Perchlorate in Drinking Water (United States)

    Izadyar, Anahita; Kim, Yushin; Ward, Michelle M.; Amemiya, Shigeru


    The inexpensive and disposable electrode based on a double-polymer-modified pencil lead is proposed for upper-division undergraduate instrumental laboratories to enable the highly sensitive detection of perchlorate. Students fabricate and utilize their own electrodes in the 3-4 h laboratory session to learn important concepts and methods of…

  17. Removal of Perchlorate from Water and Wastewater by Catalytic Hydrogen Gas Membrane Systems (United States)


    Quimica , Serie A: Quimica Fisica e Ingenieria Quimica , 1984. 80(2): p. 219-25. Logan, B.E. and D. LaPoint, Treatment of Perchlorate- and Nitrate...ion at iridium electrodes. Ion concentration and solution pH effects. Anales de Quimica , Serie A: Quimica Fisica e Ingenieria Quimica (1985), 81(3

  18. 高氯酸诺氟沙星铜(Ⅱ)%Norfloxacin Coppe(Ⅱ) Perchlorate

    Institute of Scientific and Technical Information of China (English)

    谢永荣; 叶琼; 熊仁根


    The hydrothermal treatment of Cu(ClO4)2·6H2O and Norfloxacin (H-Norf) afforded [Cu(H-Noff)2(ClO4)2] (1) in which center Cu has a square planar geometry while perchlorate just acts as charge balance anions. CCDC:140821.

  19. The Impact of Temperature on Anaerobic Biological Perchlorate Removal and Aerobic Polishing of the Effluent (United States)

    This abstract describes a pilot-scale evaluation of anaerobic biological perchlorate (C1O4) removal followed by aerobic effluent polishing. The anaerobic biological contactor operated for 3.5 years. During that period, two effluent polishing evaluations, lasting 311 an...

  20. The Impact of Temperature on Anaerobic Biological Perchlorate Removal and Aerobic Polishing of the Effluent - paper (United States)

    This abstract describes a pilot-scale evaluation of anaerobic biological perchlorate (C1O4) removal followed by aerobic effluent polishing. The anaerobic biological contactor operated for 3.5 years. During that period, two effluent polishing evaluations, lasting 311 an...


    The overall objective of this study was to demonstrate in a greenhouse study the potential for incorporation of perchlorate from aqueous solutions of 10, 50, 100, 500, 1,000, 5,000, and 10,000 ppb into an agricultural food crop (lettuce; Lactuca sativa), which is typically grown ...

  2. Regioselective iodination of aromatic compounds with potassium iodide in the presence of benzyltriphenylphosphonium perchlorate

    Institute of Scientific and Technical Information of China (English)

    Jalal Albadi; Masoumeh Abedini; Nasir Iravani


    A simple and efficient method for the selective iodination of various aromatic compounds by using potassium iodide in the presence of benzyltriphenylphosphonium perchlorate,is reported.This method provides several advantages such as good selectivity between ortho and para positions of aromatic compounds and high yields of the products.


    In the interest of resolving scientific questions, the EPA, the Department of Defense, the Department of Energy, and the National Aeronautics and Space Administration - members of a broader Interagency Working Group on Perchlorate led by the Office of Science and Technology Polic...

  4. Zero-Pressure Organic Superconductor: Di-(Tetramethyltetraselenafulvalenium)-Perchlorate [(TMTSF)2ClO4

    DEFF Research Database (Denmark)

    Bechgaard, Klaus; da Costa Carneiro, Kim; Olsen, Malte;


    Evidence for superconductivity in the organic conductor di-(tetramethyltetraselenafulvalenium)-perchlorate [(TMTSF)2ClO4] has been found by resistance measurements in the absence of applied pressure. For different crystals the transitions are approximately 0.3 K wide and are centered around...

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

    Directory of Open Access Journals (Sweden)

    Jianli Yang


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

  6. Review of Ammonium Dinitramide Toxicity Studies (United States)


    reproductive toxicant in rats, causing implantation failure in early gestation; follow-on studies implied that ADN is embryotoxic . EPR studies indicated that...mutagenic. 15. SUBJECT TERMS Ammonium dinitramide, ADN, toxicity, reproductive, embryotoxic , genotoxicity 16. SECURITY CLASSIFICATION OF: U 17...reproductive studies, reproduction and fertility, pre-implantation and post-implantation studies, implied that ADN is embryotoxic . A mouse embryo

  7. Detonation characteristics of ammonium nitrate products

    NARCIS (Netherlands)

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


    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

  8. Topaz concentrate desiliconization with ammonium bifluoride


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


    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

  9. Contribution of tap water to chlorate and perchlorate intake: a market basket study. (United States)

    Asami, Mari; Yoshida, Nobue; Kosaka, Koji; Ohno, Koichi; Matsui, Yoshihiko


    The contributions of water to total levels of chlorate and perchlorate intake were determined using food and water samples from a market basket study from 10 locations in Japan between 2008 and 2009. Foods were categorized into 13 groups and analyzed along with tap water. The average total chlorate intake was 333 (min. 193-max. 486) μg/day for samples cooked with tap water. The contribution of tap water to total chlorate intake was as high as 47%-58%, although total chlorate intake was less than 32% of the tolerable daily intake, 1500 μg/day for body weight of 50 kg. For perchlorate, daily intake from water was 0.7 (0.1-4.4) μg/day, which is not high compared to the average total intake of 14 (2.5-84) μg/day, while the reference dose (RfD) is 35 μg/day and the provisional maximum tolerable daily intake (PMTDI) is 500 μg/day for body weight of 50 kg. The highest intake of perchlorate was 84 μg/day, where concentrations in foods were high, but not in water. The contribution of water to total perchlorate intake ranged from 0.5% to 22%, while the ratio of highest daily intake to RfD was 240% and that to PMTDI was 17%. Eight baby formulas were also tested--total chlorate and perchlorate intakes were 147 (42-332) μg/day and 1.11 (0.05-4.5) μg/day, respectively, for an ingestion volume of 1 L/day if prepared with tap water.

  10. Removing perchlorate from samples to facilitate organics detection by pyrolitic methods (United States)

    von Kiparski, Guntram R.; Parker, David R.; Tsapin, Alexandre I.


    Thermal volatilization or pyrolysis of solid samples followed by gas chromatography-mass spectrometry (TV-GC-MS) or other downstream analyses has proven robustness and has been adopted for the extraction of organic compounds for their detection in planetary lander science missions (e.g., Viking Lander GC-MS, Phoenix TEGA, MSL SAM, and the future ExoMars MOMA). Pyrolysis to extract organic compounds from soil has limitations when oxidants co-occur in the analyzed sample unless the desired end product is CO2. Pyrolysis of such soils may result in oxidation of organics to CO2 during heating, and thus make organics characterization difficult, if not impossible. Analytical investigations seeking to identify organics in martian soils containing oxidants could benefit from the deployment of technologies that remove known and putative oxidants prior to thermal volatilization. We conducted a series of experiments in order to determine if a polymeric anion exchange resin, commonly used for removing the perchlorate anion from contaminated municipal water supplies, could sustain its substantial perchlorate removal capability while keeping organic compounds intact for downstream detection. We demonstrated that this resin can strongly bind perchlorate from aqueous solution while simultaneously leaving amino acids substantially unaltered. The perchlorate-binding resin could be easily adopted as a pre-treatment for martian soil extracts to create analytical systems with improved organics characterization capabilities compatible with existing TV-GC-MS systems. We propose this strategy to aid detection and characterization of putative martian organics co-situated with perchlorate at sampling sites.

  11. An Ion-selective Electrode for Anion Perchlorate in Thick-film Technology

    Directory of Open Access Journals (Sweden)

    Luís Gil


    Full Text Available The ionophore 1,4,7,10,13-penta(n-octyl-1,4,7,10,13-pentaazacyclopentadecane(L1 was used for the development of miniaturised perchlorate-selective electrodes in thick-film technology. Different PVC membranes containing L1 and the plasticizers o-nitrophenyloctyl ether (NPOE, dibutyl phthalate (DBP, bis(2-ethylhexylsebacate (DOS and dibutylsebacate (DBS were prepared and placed on a graphite working electrode manufactured byusing thick film serigraphic technology. The perchlorate selective electrode containing DBSas plasticizer showed a potentiometric Nernstian response of -57 mV per decade in a rangeof perchlorate concentration from 1 x 10-4 to 1 x 10-1 M with a detection limit of 5 x 10-5 M.The ion selective electrodes containing DBP and NPOE as plasticizers exhibit a workingrange from 6.3 x 10-5 to 1 x 10-1 M and 7.4 x 10-5 to 1 x 10-1 M for perchlorate, respectively,with a detection limit of ca. 2.2 x 10-5 M. For all three electrodes a response time of ca. 5 s was found. The prepared electrodes do not show appreciable decay of the slope for at least 25 days. Potentiometric selectivity coefficients (log KpotClO4-,X- with respect to the primaryanion perchlorate were evaluated using the fixed interference method. These coefficients areof the order of 10-1.7 or smaller, indicating the relatively poor interference of the differentanions studied.

  12. 21 CFR 184.1141b - Ammonium phosphate, dibasic. (United States)


    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ammonium phosphate, dibasic. 184.1141b Section 184... Listing of Specific Substances Affirmed as GRAS § 184.1141b Ammonium phosphate, dibasic. (a) Ammonium phosphate, dibasic ((NH4)2HPO4, CAS Reg. No. 7783-28-0) is manufactured by reacting ammonia with...

  13. 21 CFR 172.165 - Quaternary ammonium chloride combination. (United States)


    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Quaternary ammonium chloride combination. 172.165... HUMAN CONSUMPTION Food Preservatives § 172.165 Quaternary ammonium chloride combination. The food additive, quaternary ammonium chloride combination, may be safely used in food in accordance with...

  14. 78 FR 32690 - Certain Ammonium Nitrate From Ukraine (United States)


    ... COMMISSION Certain Ammonium Nitrate From Ukraine Determination On the basis of the record \\1\\ developed in... antidumping duty order on certain ammonium nitrate from Ukraine would be likely to lead to continuation or... Publication 4396 (May 2013), entitled Certain Ammonium Nitrate from Ukraine: Investigation No....

  15. 21 CFR 184.1296 - Ferric ammonium citrate. (United States)


    ... 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...

  16. Potential Influence of Perchlorate on Heavy Metals and Organic Carbon in Serpentine Soil; Implications for Martian Regolith (United States)

    Oze, C.; Kumarathilaka, P. R.; Indraratne, S.; Vithanage, M. S.


    Prasanna Kumarathilaka Chemical and Environmental Systems Modeling Research Group, National Institute of Fundamental Studies, Kandy, Sri LankaPerchlorate (ClO4-) concentrations as high as 1 Wt.% have been reported in Martian regolith. Perchlorate is a strong oxidizer capable of accelerating heavy and/or trace metal release into regolith/soil and reacting with organic matter/compounds (if present). Here, we assess interactions between perchlorate and an analogous Martian regolith (i.e., serpentine soil) to simulate and understand the fate of Mn, Ni and Co and organic carbon. Pre-characterized serpentine soil collected from Sri Lanka was used for this study. Incubation experiments were performed with three perchlorate concentrations (1, 0.75 and 0.5 w/w) and sequential and single extractions assessed solid phase metal fractionation in serpentine sediments after 3 weeks and 1 year, respectively. Additionally, total organic carbon (TOC) of the residues were analyzed. These experiments demonstrate a high release of Mn compared to Ni and Co. Metal concentrations in exchangeable and bioavailable fractions increased with increasing perchlorate concentrations. Exchangeable Ni, Mn and Co increased 5.9, 69.6 and 44.6% and bioavailable Ni, Mn and Co increased 5.5, 92.3 and 72.8%, respectively, after 1 year compared to 3 weeks. Additionally, TOC decreased with increasing perchlorate concentration. For example, TOC decreased by 14.3% after 1 year compared to a 3 week incubation period. Overall, this study confirms the accelerated release of metals and the removal of organic carbon with increasing perchlorate concentrations. Furthermore, this study illustrates how perchlorate may present additional challenges to current Martian life studies and the future human habitation of Mars.Prasanna Kumarathilaka Chemical and Environmental Systems Modeling Research Group, National Institute of Fundamental Studies, Kandy, Sri LankaPerchlorate (ClO4-) concentrations as high as 1 Wt.% have

  17. In situ bioremediation of nitrate and perchlorate in vadose zone soil for groundwater protection using gaseous electron donor injection technology. (United States)

    Evans, Patrick J; Trute, Mary M


    When present in the vadose zone, potentially toxic nitrate and perchlorate anions can be persistent sources of groundwater contamination. Gaseous electron donor injection technology (GEDIT), an anaerobic variation of petroleum hydrocarbon bioventing, involves injecting electron donor gases, such as hydrogen or ethyl acetate, into the vadose zone, to stimulate biodegradation of nitrate and perchlorate. Laboratory microcosm studies demonstrated that hydrogen and ethanol promoted nitrate and perchlorate reduction in vadose zone soil and that moisture content was an important factor. Column studies demonstrated that transport of particular electron donors varied significantly; ethyl acetate and butyraldehyde were transported more rapidly than butyl acetate and ethanol. Nitrate removal in the column studies, up to 100%, was best promoted by ethyl acetate. Up to 39% perchlorate removal was achieved with ethanol and was limited by insufficient incubation time. The results demonstrate that GEDIT is a promising remediation technology warranting further validation.

  18. Dissimilatory perchlorate reduction linked to aerobic methane oxidation via chlorite dismutase (United States)

    Oremland, R. S.; Baesman, S. M.; Miller, L. G.


    The presence of methane (CH4) in the atmosphere of Mars is controversial yet the evidence has aroused scientific interest, as CH4 could be a harbinger of extant or extinct microbial life. There are various oxidized compounds present on the surface of Mars that could serve as electron acceptors for the anaerobic oxidation of CH4, including perchlorate (ClO4-). We examined the role of perchlorate, chlorate (ClO3-) and chlorite (ClO2-) as oxidants linked to CH4 oxidation. Dissimilatory perchlorate reduction begins with reduction of ClO4- to ClO2- and ends with dismutation of chlorite to yield chloride (Cl-) and molecular oxygen (O2). We explored the potential for aerobic CH4 oxidizing bacteria to couple with oxygen derived from chlorite dismutation during dissimilatory perchlorate reduction. Methane (0.2 kPa) was completely removed within several days from the N2-flushed headspace above cell suspensions of methanotrophs (Methylobacter albus strain BG8) and perchlorate reducing bacteria (Dechloromonas agitata strain CKB) in the presence of 5 mM ClO2-. Similar rates of CH4 consumption were observed for these mixed cultures whether they were co-mingled or segregated under a common headspace, indicating that direct contact of cells was not required for methane consumption to occur. We also observed complete removal of 0.2 kPa CH4 in bottles containing dried soil (enriched in methanotrophs by CH4 additions over several weeks) and D. agitata CKB and in the presence of 10 mM ClO2-. This soil (seasonally exposed sediment) collected from the shoreline of a freshwater lake (Searsville Lake, CA) demonstrated endogenous CH4 uptake as well as perchlorate, chlorate and chlorite reduction/dismutation. However, these experiments required physical separation of soil from the aqueous bacterial culture to allow for the partitioning of O2 liberated from chlorite dismutation into the shared headspace. Although dissimilatory reduction of ClO4- and ClO3- could be inferred from the

  19. Physiological and genetic description of dissimilatory perchlorate reduction by the novel marine bacterium Arcobacter sp. strain CAB. (United States)

    Carlström, Charlotte I; Wang, Ouwei; Melnyk, Ryan A; Bauer, Stefan; Lee, Joyce; Engelbrektson, Anna; Coates, John D


    A novel dissimilatory perchlorate-reducing bacterium (DPRB), Arcobacter sp. strain CAB, was isolated from a marina in Berkeley, CA. Phylogenetically, this halophile was most closely related to Arcobacter defluvii strain SW30-2 and Arcobacter ellisii. With acetate as the electron donor, strain CAB completely reduced perchlorate (ClO4(-)) or chlorate (ClO3(-)) [collectively designated (per)chlorate] to innocuous chloride (Cl(-)), likely using the perchlorate reductase (Pcr) and chlorite dismutase (Cld) enzymes. When grown with perchlorate, optimum growth was observed at 25 to 30°C, pH 7, and 3% NaCl. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) preparations were dominated by free-swimming straight rods with 1 to 2 polar flagella per cell. Strain CAB utilized a variety of organic acids, fructose, and hydrogen as electron donors coupled to (per)chlorate reduction. Further, under anoxic growth conditions strain CAB utilized the biogenic oxygen produced as a result of chlorite dismutation to oxidize catechol via the meta-cleavage pathway of aerobic catechol degradation and the catechol 2,3-dioxygenase enzyme. In addition to (per)chlorate, oxygen and nitrate were alternatively used as electron acceptors. The 3.48-Mb draft genome encoded a distinct perchlorate reduction island (PRI) containing several transposases. The genome lacks the pcrC gene, which was previously thought to be essential for (per)chlorate reduction, and appears to use an unrelated Arcobacter c-type cytochrome to perform the same function. IMPORTANCE The study of dissimilatory perchlorate-reducing bacteria (DPRB) has largely focused on freshwater, mesophilic, neutral-pH environments. This study identifies a novel marine DPRB in the genus Arcobacter that represents the first description of a DPRB associated with the Campylobacteraceae. Strain CAB is currently the only epsilonproteobacterial DPRB in pure culture. The genome of strain CAB lacks the pcrC gene found in all

  20. Oxygen and chlorine isotopic fractionation during perchlorate biodegradation: Laboratory results and implications for forensics and natural attenuation studies (United States)

    Sturchio, N.C.; Böhlke, J.K.; Beloso, A.D.; Streger, S.H.; Heraty, L.J.; Hatzinger, P.B.


    Perchlorate is a widespread environmental contaminant having both anthropogenic and natural sources. Stable isotope ratios of O and Cl in a given sample of perchlorate may be used to distinguish its source(s). Isotopic ratios may also be useful for identifying the extent of biodegradation of perchlorate, which is critical for assessing natural attenuation of this contaminant in groundwater. For this approach to be useful, however, the kinetic isotopic fractionations of O and Cl during perchlorate biodegradation must first be determined as a function of environmental variables such as temperature and bacterial species. A laboratory study was performed in which the O and Cl isotope ratios of perchlorate were monitored as a function of degradation by two separate bacterial strains (Azospira suillum JPLRND and Dechlorospirillum sp. FBR2) at both 10??C and 22??C with acetate as the electron donor. Perchlorate was completely reduced by both strains within 280 h at 22??C and 615 h at 10??C. Measured values of isotopic fractionation factors were ??18O = -36.6 to -29.0??? and ??37Cl = -14.5 to -11.5???, and these showed no apparent systematic variation with either temperature or bacterial strain. An experiment using 18O-enriched water (??18O = +198???) gave results indistinguishable from those observed in the isotopically normal water (??18O = -8.1???) used in the other experiments, indicating negligible isotope exchange between perchlorate and water during biodegradation. The fractionation factor ratio ??18O/??37Cl was nearly invariant in all experiments at 2.50 ?? 0.04. These data indicate that isotope ratio analysis will be useful for documenting perchlorate biodegradation in soils and groundwater. The establishment of a microbial fractionation factor ratio (??18O/??37Cl) also has significant implications for forensic studies. ?? 2007 American Chemical Society.

  1. Adsorption of perchlorate from aqueous solution by the calcination product of Mg/(Al-Fe) hydrotalcite-like compounds. (United States)

    Yang, Yiqiong; Gao, Naiyun; Chu, Wenhai; Zhang, Yongji; Ma, Yan


    The calcination products containing Mg(II), Al(III), and Fe(III) in the brucite-like layers with varying Mg/Al/Fe molar ratios at 550°C were used as the adsorbent to remove perchlorate from aqueous solution, while the Mg/(Al-Fe) hydrotalcite compounds were synthesized by co-precipitation method at a constant pH value. The Mg/(Al-Fe) hydrotalcite compounds (HMAF) were characterized by XRD, FT-IR and TG-DTA. The characteristics showed that the layered double hydroxides structures in the HMAF were lost during calcination at 550°C, but were reconstructed subsequent to adsorption of perchlorate, indicating that the 'memory effect' appeared to play an important role in perchlorate adsorption. Batch adsorption studies were conducted under various equilibration conditions, such as molar ratios of Mg/Al/Fe, calcined temperature, different initial solution pH, adsorbent dose, initial perchlorate concentration, and co-existing anions. It was found that the existence of ferric iron in calcined Mg/(Al-Fe) hydrotalcite compound (CHMAF) was favorable to removal of perchlorate from water, and the best ratio of Mg/Al/Fe is 3:0.8:0.2 (CHMAF5%). This study demonstrated that the calcination product of Mg/(Al-Fe) hydrotalcite-like compound was a promising adsorbent for control of the perchlorate pollution in water.

  2. Quaternary ammonium compounds – New occupational hazards

    Directory of Open Access Journals (Sweden)

    Agnieszka Lipińska-Ojrzanowska


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

  3. Detonation Properties of Ammonium Dinitramide (ADN) (United States)

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


    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.

  4. Removal of an acid fume system contaminated with perchlorates located within hot cell

    Energy Technology Data Exchange (ETDEWEB)

    Rosenberg, K.E.; Henslee, S.P.; Vroman, W.R.; Krsul, J.R.; Michelbacher, J.A.; Knighton, G.C.


    An add scrubbing system located within the confines of a highly radioactive hot cell at Argonne National Laboratory-West (ANL-W) was remotely removed. The acid scrubbing system was routinely used for the dissolution of irradiated reactor fuel samples and structural materials. Perchloric acid was one of the acids used in the dissolution process and remained in the system with its inherent risks. Personnel could not enter the hot cell to perform the dismantling of the acid scabbing system due to the high radiation field and the explosion potential associated with the perchlorates. A robot was designed and built at ANL-W and used to dismantle the system without the need for personnel entry into the hot cell. The robot was also used for size reduction of removed components and loading of the removed components into waste containers.

  5. The processing, properties and use of the pyrotechnic mixture titanium subhydride/potassium perchlorate

    Energy Technology Data Exchange (ETDEWEB)

    Massis, T.M.


    Development of this pyrotechnic occurred because of the need for a static insensitive material to meet personnel safety requirements and related system safety issues in nuclear weapon energetic material component designs. Ti subhydride materials are made by the thermal dehydrding of commercial Ti hydride powder to the desired equivalent hydrogen composition in the Ti lattice. These Ti subhydrides, when blended with K perchlorate, meet the static insensitivity requirement of not being initiated from an equivalent human body electrostatic discharge. Individual material and blend qualification requirements provide a reproducible material from lot to lot. These pyrotechnic formulations meet the high reliability requirements (0.9995) for initiation and performance parameters and have the necessary stability and compatibility to meet long lived requirements of more than 25 years. Various experiences and problems are also discussed that have led to a mature technology for Ti subhydride/K perchlorate during its use in energetic material component designs.

  6. Research Advances: Perchlorate in Dairy and Breast Milk Samples; NO Glow on Mars; Physical Chemistry to the Rescue: Differentiating Nicotinic and Cholinergic Agonists (United States)

    King, Angela G.


    Perchlorate levels in milk suggest widespread presence of the chemical. NO emissions indicate circulation in Martian atmosphere. Modeling reveals subtle differences in drug membrane receptor interactions.

  7. Widespread occurrence of perchlorate in water, foodstuffs and human urine collected from Kuwait and its contribution to human exposure. (United States)

    Alomirah, Husam F; Al-Zenki, Sameer F; Alaswad, Marivi C; Alruwaih, Noor A; Wu, Qian; Kannan, Kurunthachalam


    Perchlorate is a thyroid hormone-disrupting compound and is reported to occur widely in the environment. Little is known on human exposure to perchlorate in Kuwait. In this study, 218 water samples, 618 commonly consumed foodstuffs and 532 urine samples collected from Kuwait were analysed to assess the exposure of the Kuwaiti population to perchlorate. For the estimation of daily intake of perchlorate, food consumption rates were obtained from the National Nutrition Survey in the State of Kuwait (NNSSK). The results showed that leafy vegetables accounted for a major share of perchlorate exposure among the Kuwaiti population at 0.062 µg kg(-)(1) bw day(-)(1) (36.2%), followed by fruits at 0.026 µg kg(-)(1) bw day(-)(1) (15.3%) and non-leafy vegetables at 0.017 µg kg(-)(1) bw day(-)(1) (10.1%). The urinary perchlorate geometric mean (GM) concentrations ranged from 8.51 to 17.1 µg l(-)(1) for the five age groups, which were higher than those reported in other countries. The estimated urinary perchlorate exposure for the Kuwaiti general population was 0.42 µg kg(-)(1) bw day(-)(1), which was higher than that reported for the United States. The dietary intake of perchlorate for the Kuwaiti population ranged from 0.14 to 0.67 µg kg(-)(1) bw day(-)(1) for the five age groups, with a mean total daily intake of 0.17 µg kg(-)(1) bw day(-)(1) for the general population. The highest estimated dietary mean daily intake of perchlorate (0.67 µg kg(-)(1) bw day(-)(1)) was found for children at 3-5 years. The estimated dietary perchlorate exposure in Kuwait is higher than the recommended mean reference dose (RfD) but lower than that of provisional maximum tolerable daily intake (PMTDI) set by the Joint FAO/WHO Expert Committee on Food Additives (JECFA).

  8. Natural Attenuation of Perchlorate in Groundwater: Processes, Tools and Monitoring Techniques (United States)


    to Aquifer Material..................................................................... 14 3.4.3 Biodegradation Processes...perchlorate is occurring. In situ columns isolate an intact column of soil and groundwater from the rest of the aquifer and can be used to monitor the...Natural Attenuation of MTBE in the Subsurface under Methanogenic Conditions. USEPA, EPA/600/R-00/006. • Pennington, J.C. et al., 1999. Draft Protocol

  9. Sweet and Sour: Attenuating Sulfidogenesis in an Advective Flow Column System with Perchlorate or Nitrate Treatment (United States)

    Engelbrektson, A. L.; Hubbard, C. G.; Piceno, Y.; Boussina, A.; Jin, Y.; Dubinsky, E. A.; Tom, L.; Hu, P.; Conrad, M. E.; Anderson, G. L.; Coates, J. D.


    Hydrogen sulfide (H2S) biogenesis in oil reservoirs is a primary cause of souring and of associated costs in reservoir and pipeline maintenance. In addition to the corrosive effects of the H2S itself, abiotic and biological oxidation also generates sulfuric acid, further degrading metallic surfaces. Amending these environments with perchlorate (ClO4-) resolves these problems by inhibition of biological sulfate reduction and re-oxidation of H2S to elemental sulfur by dissimilatory (per)chlorate reducing bacteria (DPRB). Triplicate flow through columns packed with San Francisco bay sediment were flushed with bay water ([SO4=] = 25-30 mM) containing yeast extract with 50 mM inhibitor concentrations (NO3-or ClO4-) decreasing to 25 mM and finally 12.5 mM. Influent and effluent geochemistry was monitored and DNA was prepared from the sediment bed for microbial community analysis. Souring was reversed by both treatments (at 50 mM) compared to the control columns that had no ion addition. Nitrate began to re-sour when treatment concentration was decreased to 25 mM but treatment had to be decreased to 12.5 mM before the perchlorate treated columns began to re-sour. However, the treated columns re-soured to a lesser extent than the control columns. Phylochip microbial community analyses indicated microbial community shifts and phylogenetic clustering by treatment. Isotopic analysis of sulfate showed trends that broadly agreed with the geochemistry but also suggested further sulfur cycling was occurring. This study indicates that perchlorate shows great promise as an inhibitor of sulfidogenesis in natural communities and provides insight into which organisms are involved in this process.

  10. Potentiometric Electronic Tongue to Resolve Mixtures of Sulfide and Perchlorate Anions



    This work describes the use of an array of potentiometric sensors and an artificial neural network response model to determine perchlorate and sulfide ions in polluted waters, by what is known as an electronic tongue. Sensors used have been all-solid-state PVC membrane selective electrodes, where their ionophores were different metal-phtalocyanine complexes with specific and anion generic responses. The study case illustrates the potential use of electronic tongues in the quantification of mi...

  11. 1-Benzyl­piperazine-1,4-diium bis­(perchlorate) monohydrate (United States)

    Kaabi, Kamel; El Glaoui, Meher; Jeanneau, Erwann; Rzaigui, Mohamed; Ben Nasr, Cherif


    In the title compound, C11H18N2 2+·2ClO4 −·H2O, one perchlor­ate anion is disordered over two orientations in a 0.66 (3):0.34 (3) ratio. Inter­molecular O—H⋯O, N—H⋯O and C—H⋯O hydrogen bonds link the cations, anions and water mol­ecules into ribbons extending along [100]. PMID:21587939

  12. Composition change of uranium perchlorates with organic ligands upon mechanochemical activation of exchange processes (United States)

    Zazhogin, A. P.; Zazhogin, A. A.; Komyak, A. I.; Umreiko, D. S.


    Results of studies on the effect of mechanochemical activation of ligand exchange processes in uranyl perchlorate-dimethylsulfoxide are presented. Spectroscopic data show that mechanical activation of the exchange process in this system results in the replacement of H2O in the first coordination sphere of uranyl UO{2/2+} by DMSO to form nanocrystals with a defined ligand sphere. Possible factors governing the noted features are considered.

  13. The ionic product of water in highly concentrated sodium perchlorate solutions. (United States)

    Turonek, M L; Hefter, G T; May, P M


    The ionic product of water, pK(w)=-log[H(+)][OH(-)], has been determined in aqueous solutions of sodium perchlorate over the concentration range of 1.0-8.0 M at 25 degrees C from high-precision potentiometric titrations carried out in cells with liquid junction using both glass and hydrogen electrodes. The glass electrode results are systematically lower probably as a result of interference by Na(+) ions.


    Institute of Scientific and Technical Information of China (English)

    LI Yongjun; FU Yingwen; FANG Shibi; JIANG Yingyan


    Complex films of crosslinked poly(methylsiloxane-co-ethylene oxide) and lithium perchlorate were prepared. These solid state polymeric electrolytes show a markedly higher ionic conductivity, and excellent flexibility. The ionic conductivity of the network films closed to 10-5 Scm-1 at room temperature. The effects of Li + content, species and contents of crosslinking agents, molecular weight of poly(ethylene oxide)and temperature on the ionic conductivity of the network films were also investigated.

  15. Optimization of Perchlorate Biodegradation: Performance and Cost Assessment for the Thiokol Prototype (United States)


    and startup on December 8, 1997. Incorporation of this prototype into the Thiokol’s perchlorate recovery and wastewater treatment processes has...carbohydrate byproduct (CBP), was identified and evaluated as the best replacement for the brewer’s yeast and cheese whey mixture in use at that time. CBP...was converted from the yeast- whey nutrient blend to CBP in May 1999. Since conversion, good performance has been maintained. Actual nutrient and

  16. Field Demonstration of a Novel Biotreatment Process for Perchlorate Reduction in Groundwater (United States)


    Certification Program FeCO3 siderite FOB freight on board ID inside diameter Mo molybdenum MPN most probably number NaHCO3 sodium bicarbonate...of an organic substrate.  Possibility of treating both perchlorate and possible co-contaminants such as nitrate, chlorinated solvents such as TCE...continuously extracted from a single well, from where it was distributed to the different demonstration projects. The water average contaminant

  17. Comparative assessment of the environmental sustainability of existing and emerging perchlorate treatment technologies for drinking water. (United States)

    Choe, Jong Kwon; Mehnert, Michelle H; Guest, Jeremy S; Strathmann, Timothy J; Werth, Charles J


    Environmental impacts of conventional and emerging perchlorate drinking water treatment technologies were assessed using life cycle assessment (LCA). Comparison of two ion exchange (IX) technologies (i.e., nonselective IX with periodic regeneration using brines and perchlorate-selective IX without regeneration) at an existing plant shows that brine is the dominant contributor for nonselective IX, which shows higher impact than perchlorate-selective IX. Resource consumption during the operational phase comprises >80% of the total impacts. Having identified consumables as the driving force behind environmental impacts, the relative environmental sustainability of IX, biological treatment, and catalytic reduction technologies are compared more generally using consumable inputs. The analysis indicates that the environmental impacts of heterotrophic biological treatment are 2-5 times more sensitive to influent conditions (i.e., nitrate/oxygen concentration) and are 3-14 times higher compared to IX. However, autotrophic biological treatment is most environmentally beneficial among all. Catalytic treatment using carbon-supported Re-Pd has a higher (ca. 4600 times) impact than others, but is within 0.9-30 times the impact of IX with a newly developed ligand-complexed Re-Pd catalyst formulation. This suggests catalytic reduction can be competitive with increased activity. Our assessment shows that while IX is an environmentally competitive, emerging technologies also show great promise from an environmental sustainability perspective.

  18. Solubility of PdI/sub 2/ in nitrate and perchlorate solutions. [For use in spent fuels processing; solvents are water, nitric acid, calcium nitrate, and sodium perchlorate

    Energy Technology Data Exchange (ETDEWEB)

    Horner, D.E.; Mailen, J.C.; Bigelow, H.R.


    This paper reports the solubilities of PdI/sub 2/ as measured in nitric acid by a tracer technique and in water, calcium nitrate, and sodium perchlorate solutions by a specific ion electrode technique. The tracer technique measures all the soluble iodine species, whereas the specific ion electrode measures only simple iodide ions (I/sup -/). When compared on the basis of ionic strength, the values obtained in the nitrate solutions by the two methods were in reasonable agreement. The solubilities in perchlorate solution were much higher than in nitrate, possibly because of ionic equilibria involving Pd/sup 4 +/, but this was not resolved in this work. The activity product constant, K/sub ap(PdI/sub 2/)/ = (2.5 +- 0.4) x 10/sup -23/ (25/sup 0/C), was calculated from PdI/sub 2/ solubility in water. With this value and the standard electrode potentials from the literature, the free energy of formation for PdI/sub 2/ was calculated to be --13.6 kcal/mol.

  19. Stable Ammonium Bisulfate Clusters in the Atmosphere (United States)

    Vehkamäki, Hanna; Napari, Ismo; Kulmala, Markku; Noppel, Madis


    Liquid drop model based equilibrium thermodynamics predicts that in the presence of even small ammonia concentrations practically all the atmospheric sulfuric acid molecules are bound to tiny, stable ammonium-bisulfate clusters. Hitherto sulfuric acid has been believed to form hydrates with water. Thermodynamic theory predicts correctly the hydrate formation observed experimentally. Results from ab initio computer simulations contradict the thermodynamic results and also the experimental findings for cluster formation in both sulfuric acid-water and ammonia-sulfuric acid-water mixtures.

  20. Rapid measurement of perchlorate in polar ice cores down to sub-ng L(-1) levels without pre-concentration. (United States)

    Peterson, Kari; Cole-Dai, Jihong; Brandis, Derek; Cox, Thomas; Splett, Scott


    An ion chromatography-electrospray ionization-tandem mass spectrometry (IC-ESI-MS/MS) method has been developed for rapid and accurate measurement of perchlorate in polar snow and ice core samples in which perchlorate concentrations are expected to be as low as 0.1 ng L(-1). Separation of perchlorate from major inorganic species in snow is achieved with an ion chromatography system interfaced to an AB SCIEX triple quadrupole mass spectrometer operating in multiple reaction monitoring mode. Under optimized conditions, the limit of detection and lower limit of quantification without pre-concentration have been determined to be 0.1 and 0.3 ng L(-1), respectively, with a linear dynamic range of 0.3-10.0 ng L(-1) in routine measurement. These represent improvements over previously reported methods using similar analytical techniques. The improved method allows fast, accurate, and reproducible perchlorate quantification down to the sub-ng L(-1) level and will facilitate perchlorate measurement in the study of natural perchlorate production with polar ice cores in which perchlorate concentrations are anticipated to vary in the low and sub-ng L(-1) range. Initial measurements of perchlorate in ice core samples from central Greenland show that typical perchlorate concentrations in snow dated prior to the Industrial Revolution are about 0.8 ng L(-1), while perchlorate concentrations are significantly higher in recent (post-1980) snow, suggesting that anthropogenic sources are a significant contributor to perchlorate in the current environment.

  1. Mechanism of H2S Oxidation by the Dissimilatory Perchlorate-Reducing Microorganism Azospira suillum PS. (United States)

    Mehta-Kolte, Misha G; Loutey, Dana; Wang, Ouwei; Youngblut, Matthew D; Hubbard, Christopher G; Wetmore, Kelly M; Conrad, Mark E; Coates, John D


    The genetic and biochemical basis of perchlorate-dependent H2S oxidation (PSOX) was investigated in the dissimilatory perchlorate-reducing microorganism (DPRM) Azospira suillum PS (PS). Previously, it was shown that all known DPRMs innately oxidize H2S, producing elemental sulfur (S(o)). Although the process involving PSOX is thermodynamically favorable (ΔG°' = -206 kJ ⋅ mol(-1) H2S), the underlying biochemical and genetic mechanisms are currently unknown. Interestingly, H2S is preferentially utilized over physiological electron donors such as lactate or acetate although no growth benefit is obtained from the metabolism. Here, we determined that PSOX is due to a combination of enzymatic and abiotic interactions involving reactive intermediates of perchlorate respiration. Using various approaches, including barcode analysis by sequencing (Bar-seq), transcriptome sequencing (RNA-seq), and proteomics, along with targeted mutagenesis and biochemical characterization, we identified all facets of PSOX in PS. In support of our proposed model, deletion of identified upregulated PS genes traditionally known to be involved in sulfur redox cycling (e.g., Sox, sulfide:quinone reductase [SQR]) showed no defect in PSOX activity. Proteomic analysis revealed differential abundances of a variety of stress response metal efflux pumps and divalent heavy-metal transporter proteins, suggesting a general toxicity response. Furthermore, in vitro biochemical studies demonstrated direct PSOX mediated by purified perchlorate reductase (PcrAB) in the absence of other electron transfer proteins. The results of these studies support a model in which H2S oxidation is mediated by electron transport chain short-circuiting in the periplasmic space where the PcrAB directly oxidizes H2S to S(o) The biogenically formed reactive intermediates (ClO2(-) and O2) subsequently react with additional H2S, producing polysulfide and S(o) as end products.IMPORTANCE Inorganic sulfur compounds are

  2. Synthesis of novel quaternary ammonium surfactants containing adamantane

    Institute of Scientific and Technical Information of China (English)

    Jian Wei Guo; Xing Zhong; Hua Zhu; Li Juan Feng; Ying De Cui


    A series of novel quaternary ammonium surfactants containing adamantane were designed and synthesized from 1-adamantanecarboxylic acid.The structures of target surfactants were confirmed by 1H NMR,elements analysis and FTIR.Surface properties of these surfactants were investigated.Due to the lipophilicity of adamantane,the critical micelle concentration (CMC) and C20 values of the synthesized quaternary ammonium surfactants are lower than that of conventional quaternary ammonium surfactants.

  3. Reassimilation of ammonium in Lotus japonicus. (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


    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.

  4. Bioregeneration of perchlorate-laden gel-type anion-exchange resin in a fluidized bed reactor. (United States)

    Venkatesan, Arjun K; Sharbatmaleki, Mohamadali; Batista, Jacimaria R


    Selective ion-exchange resins are very effective to remove perchlorate from contaminated waters. However, these resins are currently incinerated after one time use, making the ion-exchange process incomplete and unsustainable for perchlorate removal. Resin bioregeneration is a new concept that combines ion-exchange with biological reduction by directly contacting perchlorate-laden resins with a perchlorate-reducing bacterial culture. In this research, feasibility of the bioregeneration of perchlorate-laden gel-type anion-exchange resin was investigated. Bench-scale bioregeneration experiments, using a fluidized bed reactor and a bioreactor, were performed to evaluate the feasibility of the process and to gain insight into potential mechanisms that control the process. The results of the bioregeneration tests suggested that the initial phase of the bioregeneration process might be controlled by kinetics, while the later phase seems to be controlled by diffusion. Feasibility study showed that direct bioregeneration of gel-type resin was effective in a fluidized-bed reactor, and that the resin could be defouled, reused, and repeatedly regenerated using the method applied in this research.

  5. Bioregeneration of perchlorate-laden gel-type anion-exchange resin in a fluidized bed reactor

    Energy Technology Data Exchange (ETDEWEB)

    Venkatesan, Arjun K.; Sharbatmaleki, Mohamadali [Department of Civil and Environmental Engineering, University of Nevada Las Vegas (UNLV), 4505 Maryland Parkway, Las Vegas, NV 89154-4015 (United States); Batista, Jacimaria R., E-mail: [Department of Civil and Environmental Engineering, University of Nevada Las Vegas (UNLV), 4505 Maryland Parkway, Las Vegas, NV 89154-4015 (United States)


    Selective ion-exchange resins are very effective to remove perchlorate from contaminated waters. However, these resins are currently incinerated after one time use, making the ion-exchange process incomplete and unsustainable for perchlorate removal. Resin bioregeneration is a new concept that combines ion-exchange with biological reduction by directly contacting perchlorate-laden resins with a perchlorate-reducing bacterial culture. In this research, feasibility of the bioregeneration of perchlorate-laden gel-type anion-exchange resin was investigated. Bench-scale bioregeneration experiments, using a fluidized bed reactor and a bioreactor, were performed to evaluate the feasibility of the process and to gain insight into potential mechanisms that control the process. The results of the bioregeneration tests suggested that the initial phase of the bioregeneration process might be controlled by kinetics, while the later phase seems to be controlled by diffusion. Feasibility study showed that direct bioregeneration of gel-type resin was effective in a fluidized-bed reactor, and that the resin could be defouled, reused, and repeatedly regenerated using the method applied in this research.

  6. Comparison of biotic and abiotic treatment approaches for co-mingled perchlorate, nitrate, and nitramine explosives in groundwater (United States)

    Schaefer, C. E.; Fuller, M. E.; Condee, C. W.; Lowey, J. M.; Hatzinger, P. B.


    Biological and abiotic approaches for treating co-mingled perchlorate, nitrate, and nitramine explosives in groundwater were compared in microcosm and column studies. In microcosms, microscale zero-valent iron (mZVI), nanoscale zero-valent iron (nZVI), and nickel catalyzed the reduction of RDX and HMX from initial concentrations of 9 and 1 mg/L, respectively, to below detection (0.02 mg/L), within 2 h. The mZVI and nZVI also degraded nitrate (3 mg/L) to below 0.4 mg/L, but none of the metal catalysts were observed to appreciably reduce perchlorate (˜ 5 mg/L) in microcosms. Perchlorate losses were observed after approximately 2 months in columns of aquifer solids treated with mZVI, but this decline appears to be the result of biodegradation rather than abiotic reduction. An emulsified vegetable oil substrate was observed to effectively promote the biological reduction of nitrate, RDX and perchlorate in microcosms, and all four target contaminants in the flow-through columns. Nitrate and perchlorate were biodegraded most rapidly, followed by RDX and then HMX, although the rates of biological reduction for the nitramine explosives were appreciably slower than observed for mZVI or nickel. A model was developed to compare contaminant degradation mechanisms and rates between the biotic and abiotic treatments.

  7. Development of a Screening Model for Design and Costing of an Innovative Tailored Granular Activated Carbon Technology to Treat Perchlorate-Contaminated Water (United States)


    1 Background ...Granular Activated Carbon Technology to Treat Perchlorate-Contaminated Water I. Introduction 1.1 Background Perchlorate is commonly used... Hypothyroidism is a condition where the thyroid makes insufficient amounts of these hormones with varying health effects, including impaired

  8. Returning perchlorate-contaminated fume hood systems to service. Part II. Disassembly, decontamination, disposal, and analytical procedures. (United States)

    Bader, M; Phillips, C C; Mueller, T R; Underwood, W S; Whitson, S D


    Part I presented work leading up to and including a pilot study for remediation of laboratory fume hood systems contaminated with residues from processes that used fuming perchloric acid. Since publication of Part I, three incidents involving explosions and fires related to perchlorates have come to the attention of the authors. Experience has been gained through decontamination/remediation of 41 additional systems. This article expands on previous one and includes (1) administrative details that need to be addressed before and during the execution of the decontamination itself, (2) a seven-step procedure for decontamination-remediation/disposal, (3) some precautions associated with the use of methylene blue as a diagnostic tool for perchlorates, and-specific electrode to augment or replace the methylene blue test.

  9. Light and variable 37Cl/35Cl ratios in rocks from Gale Crater, Mars: Possible signature of perchlorate (United States)

    Farley, K. A.; Martin, P.; Archer, P. D.; Atreya, S. K.; Conrad, P. G.; Eigenbrode, J. L.; Fairén, A. G.; Franz, H. B.; Freissinet, C.; Glavin, D. P.; Mahaffy, P. R.; Malespin, C.; Ming, D. W.; Navarro-Gonzalez, R.; Sutter, B.


    Cl isotope ratios measured on HCl thermally evolved from as-yet-unknown phases in sedimentary rocks and sand in Gale Crater provide unexpected insights to the Martian surficial Cl cycle. The seven samples yield δ37Cl values ranging from - 1 ± 25 ‰ to - 51 ± 5 ‰. Five analyses from two samples of the Sheepbed mudstone (Yellowknife Bay study area) are analytically indistinguishable with a mean δ37Cl of - 11 ± 7 ‰ (1 σ). In contrast, four mudstones/sandstones from the Kimberley and Pahrump study areas also yielded indistinguishable ratios, but with a mean δ37Cl of - 43 ± 6 ‰. The Rocknest sand deposit gave a highly uncertain δ37Cl value of - 7 ± 44 ‰. These light and highly variable δ37Cl values are unique among known solar system materials. Two endmember models are offered to account for these observations, and in both, perchlorate, with its extreme ability to fractionate Cl isotopes, is critical. In the first model, SAM is detecting HCl from an oxychlorine compound (e.g., perchlorate) produced from volcanic gas emissions by atmospheric chemical reactions. Similar reactions in Earth's atmosphere may be responsible for the isotopically lightest known Cl outside of this study, in perchlorate from the Atacama Desert. Some of the Gale Crater δ37Cl values are more negative than those in Atacama perchlorate, but because reaction mechanisms and associated fractionation factors are unknown, it is impossible to assess whether this difference is prohibitive. If the negative δ37Cl signal is produced in this fashion, the isotopic variability among samples could arise either from variations in the relative size of the reactant chloride and product perchlorate reservoirs, or from variations in the fraction of perchlorate reduced back to chloride after deposition. Such reduction strongly enriches 37Cl in the residual perchlorate. Perchlorate reduction alone offers an alternative endmember model that can explain the observed data if SAM measured HCl derived

  10. 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: [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: [Office of Environmental Health Hazard Assessment, California Environmental Protection Agency, 1515 Clay St. 16th Floor, Oakland, CA 94612 (United States); Cushing, Lara, E-mail: [Energy and Resources Group, 310 Barrows Hall, University of California, Berkeley, CA 93720-3050 (United States); Blount, Benjamin C., E-mail: [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: [Arsenic Health Effects Research Group, 1950 Addison St., Suite 204, University of California, Berkeley, CA 94704 (United States)


    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

  11. Formation of oxidizing species via irradiation of perchlorates using high-energy electrons and D 2 + ions (United States)

    Crandall, Parker B.; Gillis-Davis, Jeffrey J.; Kaiser, Ralf-Ingo


    The perchlorate ion (ClO4-) has garnered particular interest in recent years following the discovery of perchlorate salts in the Martian regolith at levels of 0.4-0.6 wt% by the Phoenix lander in 2006 and Mars Science Laboratory's Curiosity rover in 2013. Due to their oxidizing properties, perchlorates are suspected to play a contributing role to the surprising lack of organics on the Martian surface. In this study, magnesium perchlorate hexahydrate (Mg(ClO4)2●6H2O) samples were irradiated with monoenergetic beams of 5 keV electrons and D2+ ions separately, sequentially, and simultaneously to simulate the effects of galactic cosmic ray exposure of perchlorates. The irradiation experiments were carried out under ultra-high vacuum conditions at 50 K, after which the samples were slowly heated to 300 K (0.5 K min-1) while desorbing products were monitored by quadrupole mass spectrometry. In all cases, molecular oxygen (O2) was detected upon the onset of irradiation and again during the warmup phase. In the case of simultaneous irradiation, deuterated water (D2O) and deuterium peroxide (D2O2) were also detected as the sample was heated whereas in the D2+ experiment small amounts of D2O2 was found exclusively. When samples were irradiated sequentially, the production of D2O2 was dependent upon the sample being irradiated with D2+ ions prior to electrons. These experiments show that perchlorates are capable of producing multiple oxidizing agents (O2, D2O2) which may also account for the lack of organics on the Martian surface.

  12. Unsteady growth of ammonium chloride dendrites (United States)

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


    Growth of ammonium chloride dendrites from aqueous solution is experimentally investigated. The growth rate υ and the radius ρ of curvature of branches are measured as a function of the relative supersaturation Δ for steady and unsteady growth conditions. It is shown that the experimental results are quantitatively described by the dependences ρ=a/Δ+b, υ=cΔ2, where the factors for primary branches are a=(1.3±0.2)·10-7 m, b=(2.5±0.4)·10-7 m, and c=(2.2±0.3)·10-4 m/s. The factor c is found to be approximately 7 times smaller for the side branches than that for the primary branches.

  13. Efficient cellulose solvent: quaternary ammonium chlorides. (United States)

    Kostag, Marc; Liebert, Tim; El Seoud, Omar A; Heinze, Thomas


    Pure quaternary tetraalkylammonium chlorides with one long alkyl chain dissolved in various organic solvents constitute a new class of cellulose solvents. The electrolytes are prepared in high yields and purity by Menshutkin quaternization, an inexpensive and easy synthesis route. The pure molten tetraalkylammonium chlorides dissolve up to 15 wt% of cellulose. Cosolvents, including N,N-dimethylacetamide (DMA), may be added in large excess, leading to a system of decreased viscosity. Contrary to the well-established solvent DMA/LiCl, cellulose dissolves in DMA/quaternary ammonium chlorides without any pretreatment. Thus, the use of the new solvent avoids some disadvantages of DMA/LiCl and ionic liquids, the most extensively employed solvents for homogeneous cellulose chemistry.

  14. Hydration Structure of the Quaternary Ammonium Cations

    KAUST Repository

    Babiaczyk, Wojtek Iwo


    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.

  15. 21 CFR 73.1298 - Ferric ammonium ferrocyanide. (United States)


    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Ferric ammonium ferrocyanide. 73.1298 Section 73.1298 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL...) Identity. (1) The color additive ferric ammonium ferrocyanide is the blue pigment obtained by...

  16. 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.


    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

  17. Bis[N-(2-pyridylcarbonylpyridine-2-carboximidato]iron(III perchlorate methanol solvate

    Directory of Open Access Journals (Sweden)

    Dayu Wu


    Full Text Available In the title complex, [Fe(C12H8N3O22]ClO4·CH3OH, the iron(III ion is surrounded by two tridentate N-(2-pyridylcarbonylpyridine-2-carboximidate (bpca ligands and exhibits a distorted octahedral coordination by six bpca N atoms. A classical O—H...O hydrogen bond exists between the methanol solvent molecule and the perchlorate anion. Magnetic susceptibility measurements indicated the complex to be in the low-spin state in the temperature range 5–400 K.

  18. 2-(2-Hydroxy-3-methoxyphenyl-1H-benzimidazol-3-ium perchlorate

    Directory of Open Access Journals (Sweden)

    Chuan Chen


    Full Text Available In the title molecular salt, C14H13N2O2+·ClO4−, the ring systems in the cation are almost coplanar [dihedral angle = 5.53 (13°]. Intramolecular N—H...O and O—H...O hydrogen bonds generate S(6 and S(5 rings, respectively. In the crystal, the two H atoms involved in the intramolecular hydrogen bonds also participate in intermolecular links to acceptor O atoms of the perchlorate anions. A simple intermolecular N—H...O bond also occurs. Together, these form a double-chain structure along [101].

  19. Ecological Risk Assessment of Perchlorate in Avian Species, Rodents, Amphibians and Fish (United States)


    http://www axolotl ). 10.0 JUSTIFICATION OF TEST SYSTEM Perchlorate occurs in ground and surface waters in 44 states in the USA... axolotl ). * Sequentially numbered in order of the date that the change is effective Dept. of Biological Sciences (DBS) Box 43131 Lubbock, TX 79409...KCl, 0.025 giL; CaCh2 H20, 0.65 g/L; MgS04·7H20, 0.1 giL ( axolotl ). *Sequentially numbered in order of the date that the

  20. Purification of human genomic DNA from whole blood using sodium perchlorate in place of phenol. (United States)

    Johns, M B; Paulus-Thomas, J E


    We have developed a new, rapid method for the extraction of human genomic DNA from whole blood samples. Traditionally, genomic DNA has been extracted from blood by overnight proteinase K digestion of lysed peripheral lymphocytes followed by phenol/chloroform extraction. In addition to being time consuming, the use of phenol involves inherent risks due to the toxic nature of the reagent. Our method for the extraction of DNA from whole blood uses sodium perchlorate and chloroform instead of phenol with a significant time savings realized as well as fewer hazards to the technician. Furthermore, DNA prepared by this new method is an excellent substrate for restriction endonuclease digestion and Southern hybridization analysis.

  1. Preparation, X-ray crystallography, and thermal decomposition of some transition metal perchlorate complexes of hexamethylenetetramine. (United States)

    Singh, Gurdip; Baranwal, B P; Kapoor, I P S; Kumar, Dinesh; Fröhlich, Roland


    The perchlorate complexes of manganese, nickel, and zinc with hexamethylenetetramine (HMTA) of the general formula [M(H2O-HMTA-H2O)2(H2O-ClO4)2(H2O)2] (where M=Mn, Ni, and Zn) have been prepared and characterized by X-ray crystallography. Thermal studies were undertaken using thermogravimetry (TG), differential thermal analysis (DTA), and explosion delay (DE) measurements. The kinetics of thermal decomposition of these complexes was investigated using isothermal TG data by applying isoconversional method. The decomposition pathways of the complexes have also been proposed. These were found to explode when subjected to higher temperatures.

  2. Ammonium removal from landfill leachate by anodic oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Cabeza, Adelaida [Department of Chemical Engineering, University of Cantabria, Avda. de los Castros s/n. 39005 Santander (Spain); Urtiaga, Ane [Department of Chemical Engineering, University of Cantabria, Avda. de los Castros s/n. 39005 Santander (Spain)]. E-mail:; Rivero, Maria-Jose [Department of Chemical Engineering, University of Cantabria, Avda. de los Castros s/n. 39005 Santander (Spain); Ortiz, Inmaculada [Department of Chemical Engineering, University of Cantabria, Avda. de los Castros s/n. 39005 Santander (Spain)


    The feasibility of removing ammonium from landfill leachates by electrochemical oxidation was studied. Raw leachates and biologically/physico-chemically pretreated leachates from a municipal landfill site were treated. Boron doped diamond was used as anode and stainless steel as cathode, both electrodes with an area of 70 cm{sup 2}. The effects of the applied current density (15-90 mA cm{sup -2}), the initial ammonium concentration (480-2000 mg L{sup -1}), and the initial chloride concentration were experimentally studied. Total ammonium removal was obtained after 360 min of processing and almost half of the initial ammonium nitrogen was oxidized to nitrate. On the other hand, the concentration of chloride enhanced the rate of ammonium oxidation. In addition, the amount of N-NH{sub 4} {sup +} transformed into N-NO{sub 3} {sup -} decreased when additional chloride was provided.

  3. Seasonal patterns of ammonium regeneration from size-fractionated microheterotrophs (United States)

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


    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.

  4. 76 FR 49449 - Continuation of Antidumping Duty Order on Solid Fertilizer Grade Ammonium Nitrate From the... (United States)


    ... Nitrate From the Russian Federation AGENCY: Import Administration, International Trade Administration... duty investigation on solid fertilizer grade ammonium nitrate (``ammonium nitrate'') from the Russian... and the ITC instituted a second sunset review of the ammonium nitrate suspended investigation....

  5. 76 FR 23569 - Termination of the Suspension Agreement on Solid Fertilizer Grade Ammonium Nitrate From the... (United States)


    ... Nitrate From the Russian Federation and Notice of Antidumping Duty Order AGENCY: Import Administration... (``AD'') Investigation on Solid Fertilizer Grade Ammonium Nitrate from the Russian Federation (``the... determine whether imports of solid fertilizer grade ammonium nitrate (``ammonium nitrate'') from Russia...

  6. Diaquasodium(I perchlorate bis[μ-2-(carboxylatomethyliminomethylphenolato]bis[(3-methylpyridinecopper(II

    Directory of Open Access Journals (Sweden)

    Zhengyi Li


    Full Text Available In the title compound, [Na(H2O2]ClO4·[Cu2(C9H7NO32(C6H7N2], the CuII atom is coordinated by one N atom and two O atoms from a tridentate N-salicylideneglycinate Schiff base dianion and one N atom from a 3-methylpyridine ligand. Longer Cu...O contacts [2.680 (2 Å] complete an approximate square-based pyramidal coordination geometry around CuII, forming a dimeric complex across a centre of inversion. The dimeric complexes form stacks along the a axis, with Cu...O contacts of 3.332 (2 Å between them. The Na+ cations and perchlorate anions lie on twofold rotation axes between the stacks. The former are coordinated by two disordered water molecules (each with half-occupancy, and form Na...O contacts of 3.698 (3 Å to the perchlorate anions and Na...π contacts to neighbouring salicylideneglycinate ligands [shortest Na...C = 3.516 (3 Å].

  7. Interfacial behavior of perchlorate versus chloride ions in saturated aqueous salt solutions

    Energy Technology Data Exchange (ETDEWEB)

    Ghosal, S; Kuo, I W; Baer, M D; Bluhm, H


    In recent years combination of theoretical and experimental work have presented a novel view of the aqueous interface wherein hard and/or multiply charged ions are excluded from the interface, but large polarizable anions show interfacial enhancement relative to the bulk. The observed trend in the propensity of anions to adsorb at the air/water interface appears to be reverse of the Hofmeister series for anions. This study focuses on experimental and theoretical examination of the partitioning behavior of perchlorate (ClO{sub 4}{sup -}) and chloride (Cl{sup -}) ions at the air/water interface. We have used ambient pressure X-ray photoelectron spectroscopy technique to directly probe the interfacial concentrations of ClO{sub 4}{sup -} and Cl{sup -} ions in sodium perchlorate and sodium chloride solutions, respectively. Experimental observations are compared with first principles molecular dynamics simulations. Both experimental and simulation results show enhancement of ClO{sub 4}{sup -} ion at the interface, compared with the absence of such enhancement in the case of Cl{sup -} ion. These observations are in agreement with the expected trend in the interfacial propensity of anions based on the Hofmeister series.

  8. Adsorption of Chloride,Nitrate and Perchlorate by Variable Charge Soils

    Institute of Scientific and Technical Information of China (English)



    Two cells consisting of a chloride-selective eloectrode and a nitrate-selective electrode or of a chloride-selectrive electrode and a perchlorate-selective electrode were directly put in the soil suspension to determine the concentration rations Cl-/NO3- or Cl-/ClO4- for studying the adsorption of the three anions by variable charge soils.It was found that all the concentration ration CCl-/CNO3- and CCl-/CClO4- in suspension were smaller than unity when soil samples were in equilibrium with mixed KCl and KNO3 or KCl and KClO4 solutions of equal concentration.The order of the amount of chloride,nitrate and perchlorate adsorbed by variable charge soils was Cl->NO3->ClO4- when the soils adsorbed these anions from the solution containing equal concentrations of Cl-,NO3- and ClO4-.Such factors as the pH of the suspension,the iron oxide content of the soil etc.Could affect the amounts and the ratios of anions adsorbed.The adsorption was chiefly caused by coulombic attraction,but a covalent force between the anion and the metal atom on the surface of soil particles may also be involved,at least for Cl- ions,even for NO3- ions.

  9. Lithium perchlorate ion pairing in a model of amorphous polyethylene oxide

    Energy Technology Data Exchange (ETDEWEB)

    Halley, J.W.; Duan, Y. [School of Physics and Astronomy, University of Minnesota, Minneapolis, Minnesota 55455 (United States); Curtiss, L.A.; Baboul, A.G. [Chemistry Division, Argonne National Laboratory, Argonne, Illinois 60439 (United States)


    We report a molecular dynamics study of pairing and dynamics of lithium cation and perchlorate anion in a previously reported model of amorphous polyethylene oxide. We are particularly interested in the question of whether these ions pair in the model, as previously reported experimentally. We calculate the potential of mean force between a lithium and perchlorate ion in the system for several temperatures when a pair of ions is at various separation distances in our model. We find evidence for two minima in the potential of mean force, one at lithium{endash}chlorine separations of 3.5 {Angstrom} and about 6.5 {Angstrom}. We studied the same system with five ion pairs in the system and again find two minima at the same separation distances but in this case there is evidence of entropic effects in the binding free energy of the pairs at 3.5 {Angstrom}. A study of radial distribution functions permits us to deduce information concerning the structure of the paired states. {copyright} {ital 1999 American Institute of Physics.}

  10. Thermal Decomposition of Calcium Perchlorate/Iron-Mineral Mixtures: Implications of the Evolved Oxygen from the Rocknest Eolian Deposit in Gale Crater, Mars (United States)

    Bruck, A. M.; Sutter, B.; Ming, D. W.; Mahaffy, P.


    A major oxygen release between 300 and 500 C was detected by the Mars Curiosity Rover Sample Analysis at Mars (SAM) instrument at the Rocknest eolian deposit. Thermal decomposition of perchlorate (ClO4-) salts in the Rocknest samples are a possible explanation for this evolved oxygen release. Releative to Na-, K-, Mg-, and Fe-perchlorate, the thermal decomposition of Ca-perchlorate in laboratory experiments released O2 in the temperature range (400-500degC) closest to the O2 release temperatures observed for the Rocknest material. Furthermore, calcium perchlorate could have been the source of Cl in the chlorinated-hydrocarbons species that were detected by SAM. Different components in the Martian soil could affect the decomposition temperature of calcium per-chlorate or another oxychlorine species. This interaction of the two components in the soil could result in O2 release temperatures consistent with those detected by SAM in the Rocknest materials. The decomposition temperatures of various alkali metal perchlorates are known to decrease in the presence of a catalyst. The objective of this work is to investigate catalytic interactions on calcium perchlorate from various iron-bearing minerals known to be present in the Rocknest material

  11. Subcellular localization of ammonium transporters in Dictyostelium discoideum

    Directory of Open Access Journals (Sweden)

    Davis Carter T


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

  12. [Reasons of high concentration ammonium in Yellow River, China]. (United States)

    Zhang, Xue-qing; Xia, Xing-hui; Yang, Zhi-feng


    Ammonium nitrogen contamination is one of the major problems of the Yellow River in China. The speciation, concentration and sources of nitrogen compounds as well as the water environment conditions of the Yellow River had been analyzed to study the reasons for the fact that the ammonium nitrogen concentration was above the water quality standard. In addition, laboratory experiments had been carried out to investigate the effects of suspended sediment (SS) on nitrification rate. The results indicated that the presence of SS could accelerate the nitrification process, therefore, the effects of SS on nitrification rate was not the reason for the high level of ammonium nitrogen in the river. The excessive and continuous input of nitrogen contaminants to the river was the fundamental reason for the high concentration of ammonium nitrogen. Organic and ammonium nitrogen with high concentration inhibitted the nitrification processes. When the initial NH4+ -N concentrations were 10.1, 18.4 and 28.2 mg/L, nitrification efficiencies were 17.4%, 13.0% and 2.5%, respectively. When the initial organic nitrogen concentrations were 5.5 and 8.6 mg/L, the maximum concentrations of ammonium nitrogen produced by the oxidation of organic nitrogen would reach 0.47 and 1.69 mg/L and they would last for 2 days and 6 days, respectively. The oxygen-consuming organics and toxic substance existing in the river water could inhibit the activity of nitrifying bacteria, and thus lead to the accumulation of ammonium nitrogen. In addition, the high pH value of river water resulted in the high concentration of nonionic ammonium nitrogen which would reduce the activity of nitrifying bacteria and decrease the nitrification rates. Besides, low river runoff, low SS content and low activity of nitrifying bacteria resulted in the high level of ammonium nitrogen of the river in the low water season.

  13. Modelling an Ammonium Transporter with SCLS

    Directory of Open Access Journals (Sweden)

    Angelo Troina


    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.

  14. Antimicrobial Polymeric Materials with Quaternary Ammonium and Phosphonium Salts

    Directory of Open Access Journals (Sweden)

    Yan Xue


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

  15. Perchlorate and selected metals in water and soil within Mount Rushmore National Memorial, South Dakota, 2011–15 (United States)

    Hoogestraat, Galen K.; Rowe, Barbara L.


    Mount Rushmore National Memorial is located in the east-central part of the Black Hills area of South Dakota and is challenged to provide drinking water to about 3 million annual visitors and year-round park personnel. An environmental concern to water resources within Mount Rushmore National Memorial has been the annual aerial fireworks display at the memorial for the Independence Day holiday during 1998–2009. A major concern of park management is the contamination of groundwater and surface water by perchlorate, which is used as an oxidizing agent in firework displays. A study by the U.S. Geological Survey, in cooperation with the National Park Service, was completed to characterize the occurrence of perchlorate and selected metals (constituents commonly associated with fireworks) in groundwater and surface water within and adjacent to Mount Rushmore National Memorial during 2011–15. Concentrations of perchlorate and metals in 106 water samples (collected from 6 groundwater sites and 14 surface-water sites) and 11 soil samples (collected from 11 soil sites) are reported.Within the Mount Rushmore National Memorial boundary, perchlorate concentrations were greatest in the Lafferty Gulch drainage basin, ranging from less than 0.20 to 38 micrograms per liter (μg/L) in groundwater samples and from 2.2 to 54 μg/L in surface-water samples. Sites within the Starling Gulch drainage basin also had some evidence of perchlorate contamination, with concentrations ranging from 0.61 to 19 μg/L. All groundwater and surface-water samples within the unnamed tributary to Grizzly Bear Creek drainage basin and reference sites outside the park boundary had concentrations less than 0.20 μg/L. Perchlorate concentrations in samples collected at the 200-foot-deep production well (Well 1) ranged from 17 to 38 μg/L with a median of 23 μg/L, whereas perchlorate concentrations in samples from the 500-foot-deep production well (Well 2) ranged from 2.1 to 17 μg/L, with a median of 6

  16. 14N NQR and relaxation in ammonium nitrate (United States)

    Stephenson, David


    The complete 14N 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 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.

  17. Synthesis and Antibacterial Activity of Novel Quaternary Ammonium Pyridoxine Derivatives. (United States)

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


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

  18. Direct esterification of ammonium salts of carboxylic acids (United States)

    Halpern, Yuval


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

  19. 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


    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.

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

    Energy Technology Data Exchange (ETDEWEB)

    Stephenson, David, E-mail: [University of the West Indies, Chemistry Department (Trinidad and Tobago)


    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.

  1. 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


    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

  2. Concurrent bioremediation of perchlorate and 1,1,1-trichloroethane in an emulsified oil barrier (United States)

    Borden, Robert C.


    A detailed field pilot test was conducted to evaluate the use of edible oil emulsions for enhanced in situ biodegradation of perchlorate and chlorinated solvents in groundwater. Edible oil substrate (EOS®) was injected into a line of ten direct push injection wells over a 2-day period to form a 15-m-long biologically active permeable reactive barrier (bio-barrier). Field monitoring results over a 2.5-year period indicate the oil injection generated strongly reducing conditions in the oil-treated zone with depletion of dissolved oxygen, nitrate, and sulfate, and increases in dissolved iron, manganese and methane. Perchlorate was degraded from 3100 to 20,000 μg/L to below detection (water, sorption to the oil and adaptation of the in situ microbial community. Approximately 4 months after emulsion injection, concentrations of 1,1,1-trichloroethane (TCA), perchloroethene (PCE), trichloroethene (TCE) and their degradation products appeared to reach a quasi steady-state condition. During the period from 4 to 18 months, TCA was reduced from 30-70 μM to 0.2-4 μM during passage through the bio-barrier. However, 1-9 μM 1,1-dichloroethane (DCA) and 8-14 μM of chloroethane (CA) remained indicating significant amounts of incompletely degraded TCA were discharging from the oil-treated zone. During this same period, PCE and TCE were reduced with concurrent production of 1,2- cis-dichloroethene ( cis-DCE). However, very little VC or ethene was produced indicating reductive dechlorination slowed or stopped at cis-DCE. The incomplete removal of TCA, PCE and TCE is likely associated with the short (5-20 days) hydraulic retention time of contaminants in the oil-treated zone. The permeability of the injection wells declined by 39-91% (average = 68%) presumably due to biomass growth and/or gas production. However, non-reactive tracer tests and detailed monitoring of the perchlorate plume demonstrated that the permeability loss did not result in excessive flow bypassing around the

  3. Monitoring Performance of a Dual Wall Permeable Reactive Barrier for Treating Perchlorate and TCE (United States)

    Dowman, C. E.; Hashimoto, Y.; Warner, S.; Bennett, P.; Gandhi, D.; Szerdy, F.; Neville, S.; Fennessy, C.; Scow, K. M.


    AMEC Geomatrix, through collaboration with Aerojet General Corporation and the University of California, Davis (UCD), has performed work leading to the installation of a dual wall permeable reactive barrier (PRB) system capable of treating perchlorate and chlorinated aliphatic hydrocarbon compounds (CAHs), including trichloroethylene (TCE), at Aerojet's Area 40 site in Sacramento, California. This unique system consisted of an upgradient zero-valent iron (ZVI) permeable reactive barrier (PRB) that is intended to not only degrade CAHs, but also, provide hydrogen generated from the ZVI corrosion process, to a downgradient bio-effective PRB (carbohydrate solution circulated through a gravel-packed trench) for destroying perchlorate. The subsurface was characterized during a site investigation, and numerous logistical and site-specific challenges of installation were addressed. The site-specific challenges included installation of a passive remediation system in a remote location with no access to electricity. The selected remediation system was keyed into the undulating bedrock 20 to 25 feet below the ground surface without the use of shoring. Under a collaborative effort, UCD provided initial bench testing. AMEC Geomatrix designed and installed the dual wall system consisting of two approximately parallel 50-foot long by 2-foot thick by 25-foot deep PRB segments which are separated by about 8 feet perpendicular to the approximate direction of groundwater flow. AMEC Geomatrix performed the installation of performance monitoring network, which consisted of 21 wells, and monitored these points for a 6-month period. Monitoring and sampling techniques were designed to measure water levels and water quality parameters in the subsurface during sampling events, to better assess the hydrologic and chemical processes. The monitoring results indicate that the upgradient ZVI PRB effectively treats groundwater with TCE concentrations approaching 60 mg/L, and in addition, may

  4. Ammonium Metabolism Enzymes Aid Helicobacter pylori Acid Resistance



    The gastric pathogen Helicobacter pylori possesses a highly active urease to support acid tolerance. Urea hydrolysis occurs inside the cytoplasm, resulting in the production of NH3 that is immediately protonated to form NH4+. This ammonium must be metabolized or effluxed because its presence within the cell is counterproductive to the goal of raising pH while maintaining a viable proton motive force (PMF). Two compatible hypotheses for mitigating intracellular ammonium toxicity include (i) th...

  5. 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: [Department of Molecular Biology, University of Gdansk, Kladki 24, 80-822 Gdansk (Poland)


    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.


    This method is applicable to the identification and quantitation of perchlorate in raw and finished drinking waters. The approach used is ion chromatography with suppressed conductivity and electrospray ionization mass spectrometry (IC-ESI/MS)

  7. Mechanism and kinetics for ammonium dinitramide (ADN) sublimation: a first-principles study. (United States)

    Zhu, R S; Chen, Hui-Lung; Lin, M C


    The mechanism for sublimation of NH(4)N(NO(2))(2) (ADN) has been investigated quantum-mechanically with generalized gradient approximation plane-wave density functional theory calculations; the solid surface is represented by a slab model and the periodic boundary conditions are applied. The calculated lattice constants for the bulk ADN, which were found to consist of NH(4)(+)[ON(O)NNO(2)](-) units, instead of NH(4)(+)[N(NO(2))(2)](-), agree quite well with experimental values. Results show that three steps are involved in the sublimation/decomposition of ADN. The first step is the relaxation of the surface layer with 1.6 kcal/mol energy per NH(4)ON(O)NNO(2) unit; the second step is the sublimation of the surface layer to form a molecular [NH(3)]-[HON(O)NNO(2)] complex with a 29.4 kcal/mol sublimation energy, consistent with the experimental observation of Korobeinichev et al. (10) The last step is the dissociation of the [H(3)N]-[HON(O)NNO(2)] complex to give NH(3) and HON(O)NNO(2) with the dissociation energy of 13.9 kcal/mol. Direct formation of NO(2) (g) from solid ADN costs a much higher energy, 58.3 kcal/mol. Our calculated total sublimation enthalpy for ADN(s) → NH(3)(g) + HON(O)NNO(2)) (g), 44.9 kcal/mol via three steps, is in good agreement with the value, 42.1 kcal/mol predicted for the one-step sublimation process in this work and the value 44.0 kcal/mol computed by Politzer et al. (11) using experimental thermochemical data. The sublimation rate constant for the rate-controlling step 2 can be represented as k(sub) = 2.18 × 10(12) exp (-30.5 kcal/mol/RT) s(-1), which agrees well with available experimental data within the temperature range studied. The high pressure limit decomposition rate constant for the molecular complex H(3)N···HON(O)NNO(2) can be expressed by k(dec) = 3.18 × 10(13) exp (-15.09 kcal/mol/RT) s(-1). In addition, water molecules were found to increase the sublimation enthalpy of ADN, contrary to that found in the ammonium

  8. Potentiometric Electronic Tongue to Resolve Mixtures of Sulfide and Perchlorate Anions

    Directory of Open Access Journals (Sweden)

    Deivy Wilson


    Full Text Available This work describes the use of an array of potentiometric sensors and an artificial neural network response model to determine perchlorate and sulfide ions in polluted waters, by what is known as an electronic tongue. Sensors used have been all-solid-state PVC membrane selective electrodes, where their ionophores were different metal-phtalocyanine complexes with specific and anion generic responses. The study case illustrates the potential use of electronic tongues in the quantification of mixtures when interfering effects need to be counterbalanced: relative errors in determination of individual ions can be decreased typically from 25% to less than 5%, if compared to the use of a single proposed ion-selective electrode.

  9. Potentiometric electronic tongue to resolve mixtures of sulfide and perchlorate anions. (United States)

    Wilson, Deivy; Abbas, Mohammed N; Radwan, Abdel Latief A; del Valle, Manel


    This work describes the use of an array of potentiometric sensors and an artificial neural network response model to determine perchlorate and sulfide ions in polluted waters, by what is known as an electronic tongue. Sensors used have been all-solid-state PVC membrane selective electrodes, where their ionophores were different metal-phtalocyanine complexes with specific and anion generic responses. The study case illustrates the potential use of electronic tongues in the quantification of mixtures when interfering effects need to be counterbalanced: relative errors in determination of individual ions can be decreased typically from 25% to less than 5%, if compared to the use of a single proposed ion-selective electrode.

  10. Large Angular Jump Mechanism Observed for Hydrogen Bond Exchange in Aqueous Perchlorate Solution

    Energy Technology Data Exchange (ETDEWEB)

    Ji, Minbiao; /SLAC, PULSE /Stanford U., Phys. Dept.; Odelius3, Michael; /Stockholm U.; Gaffney1, K.J.; /aff SLAC, PULSE


    The mechanism for hydrogen bond (H-bond) switching in solution has remained subject to debate despite extensive experimental and theoretical studies. We have applied polarization-selective multidimensional vibrational spectroscopy to investigate the H-bond exchange mechanism in aqueous NaClO{sub 4} solution. The results show that a water molecule shifts its donated H-bonds between water and perchlorate acceptors by means of large, prompt angular rotation. Using a jump-exchange kinetic model, we extract an average jump angle of 49 {+-} 4{sup o}, in qualitative agreement with the jump angle observed in molecular dynamics simulations of the same aqueous NaClO{sub 4} solution.

  11. The Nitrate/Perchlorate Ratio on Mars as an Indicator for Habitability (United States)

    Stern, J. C.; Sutter, B.; McKay, C. P.; Navarro-Gonzalex, R.; Freissinet, C.; Conrad, P. G.; Mahaffy, P. R.; Archer, P. D., Jr.; Ming, D. W.; Niles, P. B.; Zorzano, M.-P.; Martin-Torres, F. J.


    Discovery of indigenous martian nitrogen in Mars surface materials has important implications for habitability and the potential development of a nitrogen cycle at some point in martian history. The Sample Analysis at Mars (SAM) instrument suite on the Mars Science Laboratory (MSL) Curiosity Rover detected evolved nitric oxide (NO) gas during pyrolysis of scooped aeolian sediments and drilled mudstone acquired in Gale Crater. The detection of NO suggests an indigenous source of fixed N, and may indicate a mineralogical sink for atmospheric N2 in the form of nitrate. The ratio of nitrate to oxychlorine species (e.g. perchlorate) may provide insight into the extent of development of a nitrogen cycle on Mars.

  12. Electrochemical synthesis and characterization of cubic magnetite nanoparticle in aqueous ferrous perchlorate medium

    Directory of Open Access Journals (Sweden)

    D. Gopi


    Full Text Available Electrochemical synthesis of cubic magnetite nanoparticle (MNP in ferrous perchlorate aqueous medium and its spectral investigations have been carried out. The structural property of MNP is evidenced by X-ray diffraction pattern shows the characteristic peaks. Further the vibrational frequencies of MNP are evaluated using FT-IR and Raman spectroscopic techniques. UV–visible spectroscopic studies show the possibility of surface plasmon resonance effect. The cubic structure of MNP has been confirmed by transmission electron microscope (TEM technique and it is also evidenced by scanning electron microscope (SEM. The as-synthesized MNP shows superparamagnetic property which is confirmed by the vibrating sample magnetometer, hence it could be useful for synthesis of very ultra superparamagnetic iron oxide solution (VUSPIO for cancer treatment.

  13. Inhibiting effects of some oxadiazole derivatives on the corrosion of mild steel in perchloric acid solution

    Energy Technology Data Exchange (ETDEWEB)

    Lebrini, Mounim [Laboratoire de Cristallochimie et Physicochimie du Solide UMR 8012 ENSCL, BP. 108, F-59652 Villeneuve d' Ascq Cedex (France); Bentiss, Fouad [Laboratoire de Cristallochimie et Physicochimie du Solide UMR 8012 ENSCL, BP. 108, F-59652 Villeneuve d' Ascq Cedex (France); Laboratoire de Chimie de Coordination et d' Analytique, Universite Chouaib Doukkali, Faculte des Sciences, B.P. 20, El Jadida (Morocco); Vezin, Herve [Laboratoire de Chimie Organique et Macromoleculaire, CNRS UMR 8009, USTL Ba-hat t C4, F-59655 Villeneuve d' Ascq Cedex (France); Lagrenee, Michel [Laboratoire de Cristallochimie et Physicochimie du Solide UMR 8012 ENSCL, BP. 108, F-59652 Villeneuve d' Ascq Cedex (France)]. E-mail:


    The efficiency of 3,5-bis(n-pyridyl)-1,3,4-oxadiazole (n-POX, n = 1, 2, 3), as corrosion inhibitors for mild steel in 1 M perchloric acid (HClO{sub 4}) have been determined by weight loss measurements and electrochemical studies. The results show that these inhibitors revealed a good corrosion inhibition even at very low concentrations. Comparison of results among those obtained by the studied oxadiazoles shows that 3-POX was the best inhibitor. Polarisation curves indicate that n-pyridyl substituted-1,3,4-oxadiazoles are mixed type inhibitors in 1 M HClO{sub 4}. The adsorption of these inhibitors follows a Langmuir isotherm model. The electronic properties of n-POX, obtained using the AM1 semi-empirical quantum chemical approach, were correlated with their experimental efficiencies using the linear resistance model (LR)

  14. 40 CFR 418.40 - Applicability; description of the ammonium nitrate subcategory. (United States)


    ... ammonium nitrate subcategory. 418.40 Section 418.40 Protection of Environment ENVIRONMENTAL PROTECTION... Ammonium Nitrate Subcategory § 418.40 Applicability; description of the ammonium nitrate subcategory. The provisions of this subpart are applicable to discharges resulting from the manufacture of ammonium...

  15. 76 FR 39847 - Solid Fertilizer Grade Ammonium Nitrate From the Russian Federation; Final Results of the... (United States)


    ... International Trade Administration Solid Fertilizer Grade Ammonium Nitrate From the Russian Federation; Final... investigation on solid fertilizer grade ammonium nitrate (``ammonium nitrate'') from the Russian Federation...: Solid Fertilizer Grade Ammonium Nitrate From the Russian Federation, 64 FR 45236 (August 19, 1999)....

  16. Novel miniaturized sensors for potentiometric batch and flow-injection analysis (FIA) of perchlorate in fireworks and propellants. (United States)

    Almeer, Saeed H M A; Zogby, Ibrahim A; Hassan, Saad S M


    Three planar miniaturized perchlorate membrane sensors (3×5 mm(2)) are prepared using a flexible Kaptan substrate coated with nitron-perchlorate (NT-ClO4) [sensor 1], methylene blue-perchlorate (MB-ClO4) [sensor II] and indium-porphyrin (In-Por) [sensor III] as electroactive materials in PVC membranes plasticized with 2-NPPE. Sensors I, II and III display near-Nernstian response for 1.0×10(-5)-1.0×10(-2), 3.1×10(-5)-1.0×10(-2) and 3.1×10(-6)-1.0×10(-2) mol L(-1) ClO4(-) with lower detection limits of 6.1×10(-6), 6.9×10(-6) and 1.2×10(-6) mol L(-1), and anionic calibration slopes of 50.9±0.4, 48.4±0.4 and 57.7±0.3 mV decade(-1), respectively. Methods for determining perchlorate using these sensors offer many attractive advantages including simplicity, flexibility, cost effectiveness, wide linear dynamic response range (0.1-1000 ppm), low detection limit (sensors show high selectivity in the presence of some inorganic ions (e.g., PO4(3-), SO4(2-), S2O3(2-), NO2(-), NO3(-), N3(-), CN(-), Cl(-), Br(-), I(-)) and automation feasibility. Indium-porphyrin based membrane sensor (sensor III) is used as a detector in a wall-jet flow injection set-up to enable accurate flow injection analysis (FIA) of perchlorate in some fireworks without interferences from the associated reducing agents (sulfur and charcoal), binders (dextrin, lactose), coloring agents (calcium, strontium, copper, iron, sodium), color brighten (linseed oil) and regulators (aluminum flakes) which are commonly used in the formulations. The sensor is also used for perchlorate assessment in some propellant powders. The results fairly agree with data obtained by ion-chromatography.

  17. Thermal Diffusivity and Specific Heat Measurements of Titanium Potassium Perchlorate Titanium Subhydride Potassium Perchlorate 9013 Glass 7052 Glass SB-14 Glass and C-4000 Muscovite Mica Using the Flash Technique.

    Energy Technology Data Exchange (ETDEWEB)

    Specht, Paul Elliott; Cooper, Marcia A.


    The flash technique was used to measure the thermal diffusivity and specific heat of titanium potassium perchlorate (TKP) ignition powder (33wt% Ti - 67wt% KP) with Ventron sup- plied titanium particles, TKP ignition powder (33wt% Ti - 67wt% KP) with ATK supplied titanium particles, TKP output powder (41wt% Ti - 59wt% KP), and titanium subhydride potassium perchlorate (THKP) (33wt% TiH 1.65 - 67wt% KP) at 25 o C. The influence of density and temperature on the thermal diffusivity and specific heat of TKP with Ventron supplied titanium particles was also investigated. Lastly, the thermal diffusivity and specific heats of 9013 glass, 7052 glass, SB-14 glass, and C-4000 Muscovite mica are presented as a function of temperature up to 300 o C.

  18. Thermal Diffusivity and Specific Heat Measurements of Titanium Potassium Perchlorate Titanium Subhydride Potassium Perchlorate 9013 Glass 7052 Glass SB-14 Glass and C-4000 Muscovite Mica Using the Flash Technique

    Energy Technology Data Exchange (ETDEWEB)

    Specht, Paul Elliott [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Cooper, Marcia A. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)


    The flash technique was used to measure the thermal diffusivity and specific heat of titanium potassium perchlorate (TKP) ignition powder (33wt% Ti - 67wt% KP) with Ventron sup- plied titanium particles, TKP ignition powder (33wt% Ti - 67wt% KP) with ATK supplied titanium particles, TKP output powder (41wt% Ti - 59wt% KP), and titanium subhydride potassium perchlorate (THKP) (33wt% TiH 1.65 - 67wt% KP) at 25°C. The influence of density and temperature on the thermal diffusivity and specific heat of TKP with Ventron supplied titanium particles was also investigated. Lastly, the thermal diffusivity and specific heats of 9013 glass, 7052 glass, SB-14 glass, and C-4000 Muscovite mica are presented as a function of temperature up to 300° C.

  19. Perchlorate and selected metals in water and soil within Mount Rushmore National Memorial, South Dakota, 2011–15 (United States)

    Hoogestraat, Galen K.; Rowe, Barbara L.


    Mount Rushmore National Memorial is located in the east-central part of the Black Hills area of South Dakota and is challenged to provide drinking water to about 3 million annual visitors and year-round park personnel. An environmental concern to water resources within Mount Rushmore National Memorial has been the annual aerial fireworks display at the memorial for the Independence Day holiday during 1998–2009. A major concern of park management is the contamination of groundwater and surface water by perchlorate, which is used as an oxidizing agent in firework displays. A study by the U.S. Geological Survey, in cooperation with the National Park Service, was completed to characterize the occurrence of perchlorate and selected metals (constituents commonly associated with fireworks) in groundwater and surface water within and adjacent to Mount Rushmore National Memorial during 2011–15. Concentrations of perchlorate and metals in 106 water samples (collected from 6 groundwater sites and 14 surface-water sites) and 11 soil samples (collected from 11 soil sites) are reported.Within the Mount Rushmore National Memorial boundary, perchlorate concentrations were greatest in the Lafferty Gulch drainage basin, ranging from less than 0.20 to 38 micrograms per liter (μg/L) in groundwater samples and from 2.2 to 54 μg/L in surface-water samples. Sites within the Starling Gulch drainage basin also had some evidence of perchlorate contamination, with concentrations ranging from 0.61 to 19 μg/L. All groundwater and surface-water samples within the unnamed tributary to Grizzly Bear Creek drainage basin and reference sites outside the park boundary had concentrations less than 0.20 μg/L. Perchlorate concentrations in samples collected at the 200-foot-deep production well (Well 1) ranged from 17 to 38 μg/L with a median of 23 μg/L, whereas perchlorate concentrations in samples from the 500-foot-deep production well (Well 2) ranged from 2.1 to 17 μg/L, with a median of 6

  20. Fractionation of bamboo hemicelluloses by graded saturated ammonium sulphate. (United States)

    Guan, Ying; Zhang, Bing; Qi, Xian-Ming; Peng, Feng; Yao, Chun-Li; Sun, Run-Cang


    The hemicelluloses were isolated with 10% KOH at 25°C from dewaxed and delignified bamboo powder. The alkali-soluble hemicelluloses from Sinocalamus affinis were fractionated by ammonium sulphate precipitation method. The bamboo alkali-soluble hemicelluloses yielded seven hemicellulosic fractions obtained at 0, 5, 15, 25, 40, 55, and 70% saturation with ammonium sulphate. It was found that the more branched hemicelluloses were precipitated at higher ammonium sulphate concentrations (55 and 70%), the more linear hemicelluloses were precipitated at lower ammonium sulphate concentrations (0, 5, 15, 25, and 40%). The molecular weights of hemicellulosic fractions become lower from 35,270 (H0) to 18,680 (H70)gmol(-1) with the increasing concentrations of saturated ammonium sulphate from 0 to 70%. Based on the FT-IR, (1)H, (13)C and 2D HSQC NMR studies, the alkali-soluble hemicelluloses were 4-O-methyl-glucuronoarabinoxylans composed of the (1→4)-linked β-d-xylopyranosyl backbone with branches at O-3 of α-L-arabinofuranosyl or at O-2 of 4-O-methyl-α-d-glucuronic acid.

  1. A maritime pine antimicrobial peptide involved in ammonium nutrition. (United States)

    Canales, Javier; Avila, Concepción; Cánovas, Francisco M


    A large family of small cysteine-rich antimicrobial peptides (AMPs) is involved in the innate defence of plants against pathogens. Recently, it has been shown that AMPs may also play important roles in plant growth and development. In previous work, we have identified a gene of the AMP β-barrelin family that was differentially regulated in the roots of maritime pine (Pinus pinaster Ait.) in response to changes in ammonium nutrition. Here, we present the molecular characterization of two AMP genes, PpAMP1 and PpAMP2, showing different molecular structure and physicochemical properties. PpAMP1 and PpAMP2 displayed different expression patterns in maritime pine seedlings and adult trees. Furthermore, our expression analyses indicate that PpAMP1 is the major form of AMP in the tree, and its relative abundance is regulated by ammonium availability. In contrast, PpAMP2 is expressed at much lower levels and it is not regulated by ammonium. To gain new insights into the function of PpAMP1, we over-expressed the recombinant protein in Escherichia coli and demonstrated that PpAMP1 strongly inhibited yeast growth, indicating that it exhibits antimicrobial activity. We have also found that PpAMP1 alters ammonium uptake, suggesting that it is involved in the regulation of ammonium ion flux into pine roots.

  2. Effects of bisphenol A on ammonium assimilation in soybean roots. (United States)

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


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

  3. Removing ammonium from water using modified corncob-biochar. (United States)

    Vu, Thi Mai; Trinh, Van Tuyen; Doan, Dinh Phuong; Van, Huu Tap; Nguyen, Tien Vinh; Vigneswaran, Saravanamuthu; Ngo, Huu Hao


    Ammonium pollution in groundwater and surface water is of major concern in many parts of the world due to the danger it poses to the environment and people's health. This study focuses on the development of a low cost adsorbent, specifically a modified biochar prepared from corncob. Evaluated here is the efficiency of this new material for removing ammonium from synthetic water (ammonium concentration from 10 to 100mg/L). The characteristics of the modified biochar were determined by Brunauer-Emmett-Teller (BET) test, Fourier transform infrared spectroscopy (FTIR) and Scanning electron microscopy (SEM). It was found that ammonium adsorption on modified biochar strongly depended on pH. Adsorption kinetics of NH4(+)-N using modified biochar followed the pseudo-second order kinetic model. Both Langmuir and Sips adsorption isotherm models could simulate well the adsorption behavior of ammonium on modificated biochar. The highest adsorption capacity of 22.6mg NH4(+)-N/g modified biochar was obtained when the biochar was modified by soaking it in HNO3 6M and NaOH 0.3M for 8h and 24h, respectively. The high adsorption capacity of the modified biochar suggested that it is a promising adsorbent for NH4(+)-N remediation from water.

  4. Difficultly Extractable Fixed Ammonium in Some Soils of China

    Institute of Scientific and Technical Information of China (English)



    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. Quaternary ammonium salt derivatives of allylphenols with peripheral analgesic effect

    Directory of Open Access Journals (Sweden)

    A. B de Oliveira


    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.

  6. Bis(μ-bis{[4-(2-pyridylpyrimidin-2-yl]sulfanyl}methanedisilver(I bis(perchlorate

    Directory of Open Access Journals (Sweden)

    Hai-Bin Zhu


    Full Text Available In the macrocyclic centrosymmetric dinuclear complex, [Ag2(C19H14N6S22](ClO42, the AgI atom, bis{[4-(2-pyridylpyrimidin-2-yl]sulfanyl}methane (2-bppt ligand and perchlorate anion each lie on a twofold rotation axis. The 2-bppt ligand chelates two four-coordinated AgI atoms through its two bipyridine-like arms. The O atoms of the perchlorate anion are disordered each over two positions of equal occupancy. Adjacent complex molecules are linked by π–π interactions between the pyridine and pyrimidine rings [centroid–centroid distance = 3.663 (8 Å].

  7. Poly[[tetrakis(μ2-pyrazine N,N′-dioxide-κ2O:O′erbium(III] tris(perchlorate

    Directory of Open Access Journals (Sweden)

    James D. Buchner


    Full Text Available The title three-dimensional coordination network, {[Er(C4H4N2O24](ClO43}n, is isostructural to that of other lanthanides. The Er+3 cation lies on a fourfold roto-inversion axis. It is coordinated in a distorted square-antiprismatic fashion by eight O atoms from bridging pyrazine N,N′-dioxide ligands. There are two unique pyrazine N,N′-dioxide ligands. One ring is located around an inversion center, and there is a a twofold rotation axis at the center of the other ring. There are also two unique perchlorate anions. One is centered on a twofold rotation axis and the other on a fourfold roto-inversion axis. The perchlorate anions are located in channels that run perpendicular to (001 and (110 and interact with the coordination network through C—H...O hydrogen bonds.

  8. Vibrational Spectroscopic Study on Ion Solvation and Association of Lithium Perchlorate in 4-Methoxymethyl-ethylene Carbonate

    Institute of Scientific and Technical Information of China (English)

    QIAO,Hong-Wei; LUAN,He-Lin; ZHOU,Zhi-Ming; YAO,Wen


    Solvation interaction and ion association in solutions of lithium perchlorate/4-methoxymethyl-ethylene carbonate(MEC)have been studied by using Infrared and Raman spectra as a function of concentration of lithium perchlorate.The splitting of ring deformation band and ring ether asymmetric stretching band,and the change of Carbonyl stretching band suggest that there should be a strong interaction between Li+ and the solvent molecules,and the site of solvation should be the oxygen atom of carbonyl group.The apparent solvation number of Li+ was calculated by using band fitting technique.The solvation number was decreased from 3.3 to 1.1 with increasing the concentration of LiClO4/MEC solutions.On the other hand,the band fitting for the ClO ̄4 band revealed the presence of contact ion pair,and free ClO ̄4 anion in the concentrated solutions.

  9. Demonstration of a Full-Scale Fluidized Bed Bioreactor for the Treatment of Perchlorate at Low Concentrations in Groundwater (United States)


    experiments. Some xiii degree of adsorption and biodegradation contributed to the treatment of both the nitrate and perchlorate. The general...based on stoichiometric biodegradation rates, feed-forward control logic is established to automatically set the electron donor and nutrient corrected. 102 High or Low Fluidization Pump discharge pressure ( PAH /L-105) FBR System Shutdown FCV-20 closes P-100 stops – fluidization

  10. Supercritical Carbon Dioxide Extraction of Coronene in the Presence of Perchlorate for In Situ Chemical Analysis of Martian Regolith (United States)

    McCaig, Heather C.; Stockton, Amanda; Crilly, Candice; Chung, Shirley; Kanik, Isik; Lin, Ying; Zhong, Fang


    The analysis of the organic compounds present in the martian regolith is essential for understanding the history and habitability of Mars, as well as studying the signs of possible extant or extinct life. To date, pyrolysis, the only technique that has been used to extract organic compounds from the martian regolith, has not enabled the detection of unaltered native martian organics. The elevated temperatures required for pyrolysis extraction can cause native martian organics to react with perchlorate salts in the regolith and possibly result in the chlorohydrocarbons that have been detected by in situ instruments. Supercritical carbon dioxide (SCCO2) extraction is an alternative to pyrolysis that may be capable of delivering unaltered native organic species to an in situ detector. In this study, we report the SCCO2 extraction of unaltered coronene, a representative polycyclic aromatic hydrocarbon (PAH), from martian regolith simulants, in the presence of 3 parts per thousand (ppth) sodium perchlorate. PAHs are a class of nonpolar molecules of astrobiological interest and are delivered to the martian surface by meteoritic infall. We also determined that the extraction efficiency of coronene was unaffected by the presence of perchlorate on the regolith simulant, and that no sodium perchlorate was extracted by SCCO2. This indicates that SCCO2 extraction can provide de-salted samples that could be directly delivered to a variety of in situ detectors. SCCO2 was also used to extract trace native fluorescent organic compounds from the martian regolith simulant JSC Mars-1, providing further evidence that SCCO2 extraction may provide an alternative to pyrolysis to enable the delivery of unaltered native organic compounds to an in situ detector on a future Mars rover.

  11. 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:; Valentin-Blasini, Liza [Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA 30341 (United States)


    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.

  12. N,N′-Bis(2-ammoniobenzylethane-1,2-diammonium–nitrate–perchlorate (1/1.5/2.5

    Directory of Open Access Journals (Sweden)

    Nancy Pérez Rodríguez


    Full Text Available The title compound, C16H26N44+·2.5ClO4−·1.5NO3−, is an organic salt in which the cation is a fully protonated tetramine. The cation lies on an inversion center and, as a consequence, both benzene rings are parallel. The central chain is found in an all-trans arrangement, a conformation different from that observed in the crystal structure of the non-protonated molecule. The charges are balanced by a mixture of nitrate and perchlorate ions. One site is occupied by an ordered perchlorate ion, while the other contains both nitrate and perchlorate ions, with occupancies of 0.75 and 0.25, respectively. In the crystal, the NH2+ groups of the cation form N—H...O hydrogen bonds with the anions. The NH3+ groups also behave as donor groups, allowing the building of chains along [100], alternating cations and disordered anions being connected via N—H...O hydrogen bonds.

  13. Microbial respiration with chlorine oxyanions: diversity and physiological and biochemical properties of chlorate- and perchlorate-reducing microorganisms. (United States)

    Liebensteiner, Martin G; Oosterkamp, Margreet J; Stams, Alfons J M


    Chlorine oxyanions are valuable electron acceptors for microorganisms. Recent findings have shed light on the natural formation of chlorine oxyanions in the environment. These suggest a permanent introduction of respective compounds on Earth, long before their anthropogenic manufacture. Microorganisms that are able to grow by the reduction of chlorate and perchlorate are affiliated with phylogenetically diverse lineages, spanning from the Proteobacteria to the Firmicutes and archaeal microorganisms. Microbial reduction of chlorine oxyanions can be found in diverse environments and different environmental conditions (temperature, salinities, pH). It commonly involves the enzymes perchlorate reductase (Pcr) or chlorate reductase (Clr) and chlorite dismutase (Cld). Horizontal gene transfer seems to play an important role for the acquisition of functional genes. Novel and efficient Clds were isolated from microorganisms incapable of growing on chlorine oxyanions. Archaea seem to use a periplasmic Nar-type reductase (pNar) for perchlorate reduction and lack a functional Cld. Chlorite is possibly eliminated by alternative (abiotic) reactions. This was already demonstrated for Archaeoglobus fulgidus, which uses reduced sulfur compounds to detoxify chlorite. A broad biochemical diversity of the trait, its environmental dispersal, and the occurrence of relevant enzymes in diverse lineages may indicate early adaptations of life toward chlorine oxyanions on Earth.

  14. Influence of rhenium speciation on the stability and activity of Re/Pd bimetal catalysts used for perchlorate reduction. (United States)

    Choe, Jong Kwon; Shapley, John R; Strathmann, Timothy J; Werth, Charles J


    Recent work demonstrates reduction of aqueous perchlorate by hydrogen at ambient temperatures and pressures using a novel rhenium-palladium bimetal catalyst immobilized on activated carbon (Re/Pd-AC). This study examines the influence of Re speciation on catalyst activity and stability. Rates of perchlorate reduction are linearly dependent on Re content from 0-6 wt %, but no further increases are observed at higher Re contents. Surface-immobilized Re shows varying stability and speciation both in oxic versus H(2)-reducing environments and as a function of Re content. In oxic solutions, Re immobilization is dictated by sorption of the Re(VII) precursor, perrhenate (ReO(4)(-)), to activated carbon via electrostatic interactions. Under H(2)-reducing conditions, Re immobilization is significantly improved and leaching is minimized by ReO(4)(-) reduction to more reduced species on the catalyst surface. X-ray photoelectron spectroscopy shows two different Re binding energy states under H(2)-reducing conditions that correspond most closely to Re(V)/Re(IV) and Re(I) reference standards, respectively. The distribution of the two redox states varies with Re content, with the latter predominating at lower Re contents where catalyst activity is more strongly dependent on Re content. Results demonstrate that both lower Re contents and the maintenance of H(2)-reducing conditions are key elements in stabilizing the active Re surface species that are needed for sustained catalytic perchlorate treatment.

  15. Detection of trace organics in Mars analog samples containing perchlorate by laser desorption/ionization mass spectrometry. (United States)

    Li, Xiang; Danell, Ryan M; Brinckerhoff, William B; Pinnick, Veronica T; van Amerom, Friso; Arevalo, Ricardo D; Getty, Stephanie A; Mahaffy, Paul R; Steininger, Harald; Goesmann, Fred


    Evidence from recent Mars missions indicates the presence of perchlorate salts up to 1 wt % level in the near-surface materials. Mixed perchlorates and other oxychlorine species may complicate the detection of organic molecules in bulk martian samples when using pyrolysis techniques. To address this analytical challenge, we report here results of laboratory measurements with laser desorption mass spectrometry, including analyses performed on both commercial and Mars Organic Molecule Analyzer (MOMA) breadboard instruments. We demonstrate that the detection of nonvolatile organics in selected spiked mineral-matrix materials by laser desorption/ionization (LDI) mass spectrometry is not inhibited by the presence of up to 1 wt % perchlorate salt. The organics in the sample are not significantly degraded or combusted in the LDI process, and the parent molecular ion is retained in the mass spectrum. The LDI technique provides distinct potential benefits for the detection of organics in situ on the martian surface and has the potential to aid in the search for signs of life on Mars.

  16. The biological activity of quaternary ammonium salts (QASs

    Directory of Open Access Journals (Sweden)

    Ewa Obłąk


    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.

  17. [The biological activity of quaternary ammonium salts (QASs)]. (United States)

    Obłak, Ewa; Gamian, Andrzej


    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 Staphylococcus aureus strains contain the plasmid-carrying genes qacA and qacB 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.

  18. Study on mechanism of isomerization between ammonium thiocyanate and thiourea (United States)

    Zhang, Chao-Zhi; Niu, Meng-Xiao


    Application of ammonium thiocyanate that can be separated from wastewater in coking plant is limited. It may isomerize to thiourea which has widely applied in industry. However, the isomerization yield is low. Moreover, the isomerization temperature is more than 145 °C. In this paper, the isomerization was investigated. The mechanism of the isomerization was supposed based on quantum chemistry calculations. Ammonia was employed as a catalyst to lower isomerization temperature and improved the yield of thiourea in the isomerization reaction. Results of quantum chemical calculation and experiments support the supposed mechanism. The mechanism can be applied in production of thiourea from isomerization of ammonium thiocyanate. The paper suggests a useful way of resourcizing ammonium thiocyanate in wastewater.

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

    Institute of Scientific and Technical Information of China (English)

    GUAN Yong-jie


    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.

  20. Performance of sulfate-dependent anaerobic ammonium oxidation

    Institute of Scientific and Technical Information of China (English)


    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.

  1. 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


    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.

  2. Steady state growth of E. Coli in low ammonium environment (United States)

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


    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.

  3. Precipitation of phenyl and phenoxypenicillin from solutions using ammonium sulfate. (United States)

    Luengo, J M


    An easy, rapid, and available method for separating 6-aminopenicillanic acid (6-APA), benzylpenicillin (penicillin G), and other related molecules from aqueous solutions or complex industrial broths is described. A high concentration of ammonium sulphate induces partially or totally the precipitation of the penicillin present in the solutions, while 6-APA, phenylacetic, and phenoxyacetic acid always remain in the supernatant. The filtration through No. 4 Pyrex glass-fiber filter or Whatman 3MM paper permits the separation of the compounds present in the supernatant from the other ones precipitated. The precipitated product was identified, in all cases, as ammonium penicillin. This method is described here for the first time.

  4. 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


    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.

  5. Aerosol isotopic ammonium signatures over the remote Atlantic Ocean (United States)

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


    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.

  6. Mutagenic activity of quaternary ammonium salt derivatives of carbohydrates (United States)

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


    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

  7. Spectroscopic study of perchlorates and other oxygen chlorides in a Martian environmental chamber (United States)

    Wu, Zhongchen; Wang, Alian; Ling, Zongcheng


    We report a study where the molecular spectral features of nine anhydrous and hydrous oxygen chlorides were analyzed both under Mars atmospheric pressure and temperature conditions in a Planetary Environment and Analysis Chamber (PEACh) and, for comparison, under ambient laboratory conditions. The goal is to understand the effect of Mars environmental conditions (mainly temperature T and CO2 pressure P) on their spectral features as determined by both Raman and NIR spectroscopy. These results will be used for in situ simultaneous identification of the Cl O4- and other intermediate oxygen chloride products generated during a dynamic electrostatic discharge (ESD) experiment. We have three major findings from the first phase of this study: (1) the ν1 Raman peak position is the most sensitive parameter for identifying the cation speciation in perchlorates (e.g., Na, Mg, Ca), the hydration state of magnesium perchlorate (e.g., Mg(ClO4)2 ṡ xH2O, x = 0 , 2 , 4 , 6), and the degree of oxidation of sodium oxygen chlorides (e.g., NaClOy, y = 1 , 2 , 3 , 4); (2) ν1 Raman peak positions of most tested hydrous and anhydrous oxygen chlorides show no detectable changes within the tested T and P ranges relevant to the environmental conditions at Mars surface and shallow subsurface, but water Raman peaks of the hydrated salts change following T decreases; (3) under the P &T conditions relevant to current surface and shallow subsurface at Mars mid-latitude regions, both Mg(ClO4)2 ṡ 6H2O and Ca(ClO4)2 ṡ 2H2O are stable against dehydration, while NaClO4 ṡ H2O dehydrates, with a dehydration rate that is a function of T which was quantified by in situ NIR spectroscopy. These results are useful for the interpretations of the data from current orbital remote sensing (Vis-NIR spectra) and from future landed missions (Raman spectra). Furthermore, we have designed a set of systematic ESD experiments to be conducted in PEACh for studying the pathways and the rates of oxygen chloride

  8. Removal of toxic ions (chromate, arsenate, and perchlorate) using reverse osmosis, nanofiltration, and ultrafiltration membranes

    KAUST Repository

    Yoon, Jaekyung


    Rejection characteristics of chromate, arsenate, and perchlorate were examined for one reverse osmosis (RO, LFC-1), two nanofiltration (NF, ESNA, and MX07), and one ultrafiltration (UF and GM) membranes that are commercially available. A bench-scale cross-flow flat-sheet filtration system was employed to determine the toxic ion rejection and the membrane flux. Both model and natural waters were used to prepare chromate, arsenate, and perchlorate solutions (approximately 100 μg L-1 for each anion) in mixtures in the presence of other salts (KCl, K2SO4, and CaCl2); and at varying pH conditions (4, 6, 8, and 10) and solution conductivities (30, 60, and 115 mS m-1). The rejection of target ions by the membranes increases with increasing solution pH due to the increasingly negative membrane charge with synthetic model waters. Cr(VI), As(V), and ClO4 - rejection follows the order LFC-1 (>90%) > MX07 (25-95%) ≅ ESNA (30-90%) > GM (3-47%) at all pH conditions. In contrast, the rejection of target ions by the membranes decreases with increasing solution conductivity due to the decreasingly negative membrane charge. Cr(VI), As(V), and ClO4 - rejection follows the order CaCl2 < KCl ≅ K2SO4 at constant pH and conductivity conditions for the NF and UF membranes tested. For natural waters the LFC-1 RO membrane with a small pore size (0.34 nm) had a significantly greater rejection for those target anions (>90%) excluding NO3 - (71-74%) than the ESNA NF membrane (11-56%) with a relatively large pore size (0.44 nm), indicating that size exclusion is at least partially responsible for the rejection. The ratio of solute radius (ri,s) to effective membrane pore radius (rp) was employed to compare ion rejection. For all of the ions, the rejection is higher than 70% when the ri,s/rp ratio is greater than 0.4 for the LFC-1 membrane, while for di-valent ions (CrO4 2 -, SO4 2 -, and HAsSO4 2 -) the rejection (38-56%) is fairly proportional to the ri,s/rp ratio (0.32-0.62) for the ESNA

  9. 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


    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.

  10. 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)


    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.

  11. 75 FR 14082 - Ammonium Salts of Fatty Acids (C8 (United States)


    ... diet of humans, animals, and plants and currently have Food and Drug Administration and EPA approved.../kg/day (6 times the limit dose of 1,000 mg/kg/day) on days 2 to 13 of pregnancy and musculo-skeletal... plants. Ammonium salts of fatty acid are not likely to persist in the environment and are expected to...

  12. Increase of water resistance of ammonium nitrate explosives

    Directory of Open Access Journals (Sweden)

    Zulkhair Mansurov


    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.

  13. Characterization of ammonium polyuranate powders from a continuous precipitator

    Energy Technology Data Exchange (ETDEWEB)

    Oolman, T.


    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.

  14. Synthetic receptors for ammonium ions using dynamic combinatorial chemistry

    NARCIS (Netherlands)

    Hamieh, Saleh


    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

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

    NARCIS (Netherlands)

    Breteler, H.


    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

  16. Treating leachate mixture with anaerobic ammonium oxidation technology

    Institute of Scientific and Technical Information of China (English)

    ZHANG Hong-guo; ZHOU Shao-qi


    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.

  17. Growth features of ammonium hydrogen -tartrate single crystals

    Indian Academy of Sciences (India)

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


    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.

  18. Global modeling of nitrate and ammonium aerosols using EQSAM3 (United States)

    Xu, L.; Penner, J. E.


    Atmospheric aerosols, particles suspending in air, are important as they affect human health, air quality, and visibility as well as climate. Sulfate, nitrate, ammonium, chloride and sodium are among the most important inorganic aerosol species in the atmosphere. These compounds are hygroscopic and absorb water under almost all ambient environmental conditions. The uptake of water alters the aerosol size, and causes water to become the constituent with the largest atmospheric aerosol mass, especially when the aerosols grow into fog, haze or clouds. Furthermore, several global model studies have demonstrated that rapid increases in nitrogen emissions could produce enough nitrate in aerosols to offset the expected decline in sulfate forcing by 2100 for the extreme IPCC A2 scenario (Bauer et al., 2007). Although nitrate and ammonium were identified as significant anthropogenic sources of aerosols by a number of modeling studies, most global aerosol models still exclude ammonium-nitrate when the direct aerosol forcing is studied. In this study, the computationally efficient equilibrium model, EQSAM3, is incorporated into the UMICH-IMPACT-nitrate model using the hybrid dynamical solution method (Feng and Penner, 2007). The partitioning of nitrate and ammonium along with the corresponding water uptake is evaluated by comparing the model to the EQUISOLVE II method used in Feng and Penner (2007). The model is also evaluated by comparison with the AERONET data base and satellite-based aerosol optical depths.

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

    NARCIS (Netherlands)

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


    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

  20. Ferroelectric Polarization Switching Dynamics and Domain Growth of Triglycine Sulfate and Imidazolium Perchlorate

    KAUST Repository

    Ma, He


    The weak bond energy and large anisotropic domain wall energy induce many special characteristics of the domain nucleation, growth, and polarization switch in triglycine sulfate (TGS) and imidazolium perchlorate (IM), two typical molecular ferroelectrics. Their domain nucleation and polarization switch are rather slower than those of conventional oxide ferroelectrics, which may be due to the weaker bond energy of hydrogen bond or van der Waals bond than that of ionic bond. These chemical bonds dominate the elastic energy, with the latter being an important component of domain wall energy and playing an important role in domain nucleation and domain growth. The ratio of anisotropic domain wall energy to Gibbs free energy is large in TGS and IM, which allows a favorable domain shape and a special domain evolution under a certain electric field. Therefore, this study not only sheds light on the physical nature but also indicates the application direction for molecular ferroelectrics. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

  1. Synthesis, growth and characterization of a nonlinear optical crystal: l-Leucinium perchlorate

    Directory of Open Access Journals (Sweden)

    P. Baskaran


    Full Text Available An amino acid based semiorganic nonlinear optical family single crystal of l-leucinium perchlorate (LLPCl was grown by the solvent evaporation method at ambient temperature. Good optical quality single crystals up to a size of 6 mm × 5 mm × 3 mm were obtained. The single-crystal XRD analysis shows that the grown crystals have a monoclinic structure. Fourier transform infrared (FTIR spectral analysis and UV–vis spectral studies were also carried out. Microhardness mechanical studies show that the hardness number (Hv of a LLPCl single crystal decreases with the load as measured by the Vickers microhardness method. The dielectric properties of the grown crystal were analysed by varying the frequency. Photoconductivity analysis gives the variation of the photocurrent and dark current. The nonlinear optical properties were studied using the Kurtz and Perry powder method and the second harmonic generation efficiency was found to be 2.6 times higher than that of KDP crystals.

  2. (μ-1,4,7,10-Tetraoxacyclododecanebis[(1,4,7,10-tetraoxacyclododecanelithium] bis(perchlorate

    Directory of Open Access Journals (Sweden)

    Ilia A. Guzei


    Full Text Available 12-Crown-4 ether (12C4 and LiClO4 combine to form the ionic title compound, [Li2(C8H16O43](ClO42, which is composed of discrete Li/12C4 cations and perchlorate anions. In the [Li2(12C43]2+ cation there are two peripheral 12C4 ligands, which each form four Li—O bonds with only one Li+ atom. Additionally there is a central 12C4 in which diagonal O atoms form one Li—O bond each with both Li+ atoms. Therefore each Li+ atom is pentacoordinated in a distorted square-pyramidal geometry, forming four longer bonds to the O atoms on the peripheral 12C4 and one shorter bond to an O atom of the central 12C4. The cation occupies a crystallographic inversion centre located at the center of the ring of the central 12C4 ligand. The Li+ atom lies above the cavity of the peripheral 12C4 by 0.815 (2 Å because it is too large to fit in the cavity.

  3. Morphological control of zinc tricarbohydrazide perchlorate crystals:Theoretical and experimental study

    Institute of Scientific and Technical Information of China (English)

    LIU Rui; QI ShuYuan; ZHANG TongLai; ZHOU ZunNing; YANG Li; ZHANG JianGuo


    The theoretical crystal-morphology of zinc tricarbohydrazide perchlorate (ZnCP) was studied using the morphology simulation software.The growth trends and surface characteristics were calculated using the Bravais-Friedel-Donnay-Harker (BFDH),Growth Morphology,and Equilibrium Morphology methods; these provide theoretical guidance for the choice of crystal-control reagents.On the basis of the simulations,experiments were carried out to study the effects of five different crystal-control reagents,including carboxymethylcellulose (A),polyacrylamide (B),dextrin (C),Tween 40 (D),and Tween 60 (E),in the control of the crystal-morphology of ZnCP.Mixtures of two reagents and higher temperatures were used to further optimize the ZnCP crystals.The results show that ZnCP crystals are well dispersed,and have a large apparent density and regular crystal-morphology under the control of a mixture of reagents A and E in a mass ratio of 1 ∶ 4 at 80℃.

  4. Widespread presence of naturally occurring perchlorate in high plains of Texas and New Mexico (United States)

    Rajagopalan, S.; Anderson, T.A.; Fahlquist, L.; Rainwater, K.A.; Ridley, M.; Jackson, W.A.


    Perchlorate (ClO4-) occurrence in groundwater has previously been linked to industrial releases and the historic use of Chilean nitrate fertilizers. However, recently a number of occurrences have been identified for which there is no obvious anthropogenic source. Groundwater from an area of 155 000 km2 in 56 counties in northwest Texas and eastern New Mexico is impacted by the presence of ClO4-. Concentrations were generally low (anions (e.g., IO3-, Cl-, SO4-2) and ClO4-. The ClO4- distribution appears to be mainly related to evaporative concentration and unsaturated transport. This process has led to higher ClO4- and other ion concentrations in groundwater where the water table is relatively shallow, and in areas with lower saturated thickness. Irrigation may have accelerated this process in some areas by increasing the transport of accumulated salts and by increasing the number of evaporative cycles. Results from this study highlight the potential for ClO4- to impact groundwater in arid and semiarid areas through long-term atmospheric deposition. ?? 2006 American Chemical Society.

  5. (2,2′-Bipyridine(2-formyl-6-methoxyphenolatonickel(II perchlorate

    Directory of Open Access Journals (Sweden)

    Cui-Juan Wang


    Full Text Available In the title compound, [Ni(C8H7O3(C10H8N2]ClO4, the NiII atom is in a slightly distorted square-planar coordination by two N atoms from the 2,2′-bipyridine (bipy ligand and two O atoms from the deprotonated 2-formyl-6-methoxyphenolate (mbd ligand. The bipy ligand is nearly coplanar with the NiII square plane, the Ni atom being only 0.042 (2 Å from the mean plane, whereas the benzaldehyde plane is folded with respect to the square plane, making a dihedral angle of 19.17 (8°. One of the O atoms of the perchlorate anion is involved in a weak interaction with the Ni atom, with an Ni—O distance of 2.5732 (18 Å. The packing is stabilized by weak C—H...O interactions.

  6. Maximizing ammonium nitrogen removal from solution using different zeolites. (United States)

    Penn, Chad J; Warren, Jason G; Smith, Savannah


    Zeolite minerals are ideal for removing ammonium nitrogen (NH4(+)-N) from animal wastes, leachates, and industrial effluents. The objectives of this study were to compare NH4+ removal and kinetics among several commercially available zeolites under various conditions and determine if calorimetry could provide information regarding kinetics of NH4+ removal. Ammonium sorption onto potassium (K) saturated zeolites was compared using synthetic vs. natural swine effluent and with either traditional batch-shaken system or a "tea bag" approach in which zeolites were contained in a mesh sack and suspended in a solution of swine effluent. Ammonium sorption was measured at four retention times using a flow-through system, and the resulting heat response was measured using isothermal calorimetry. Ammonium removal was not significantly different in synthetic vs. natural swine effluent. Ammonium removal was lower in batch-stirred compared to batch-shaken systems, suggesting that diffusion between particles was rate-limiting in the former system. Flow-through cells possessing contact times > 100 s displayed greater NH4+ sorption than batch systems, suggesting that maintaining high NH4+ concentration in solution, removal of exchange products, and sufficient reaction time are critical to maximizing NH4+ removal by zeolites. Within 100 s after NH4+ addition, endothermic heat responses indicated that NH4(+)-K+ exchange had peaked; this was followed by significant heat rate reduction for 50 min. This confirmed findings of an initial fast NH4(+)-K+ exchange followed by a slower one and suggests the 100-s period of rapid reaction is an indicator of the minimum flow through retention time required to optimize NH4+ sorption to zeolites used in this study.

  7. Recycle use of magnesium ammonium phosphate to remove ammonium nitrogen from rare-earth wastewater. (United States)

    Huang, H M; Xiao, X M; Yan, B


    This paper presents a recycle MAP process (magnesium ammonium phosphate) to remove NH4-N from a typical rare-earth wastewater. The optimum conditions for the MAP precipitation and recycle use of the MAP with a newly-designed process were investigated in laboratory. The results showed that the pH value and dosages of P (phosphate) and Mg reagents have a significant influence on NH4-N removal, with a maximum removal efficiency of 99.4% at the conditions of pH=9 and Mg:N:P molar ratio=1.2:1:1.2. In the process of recycle use of the MAP, adding some HCl to dissolve MAP decomposition residues could effectively enhance NH4-N removal. The NH4-N removal efficiency reached 99.6% by adding an HCl amount of H+:OH- molar ratio=0.8 into the reused MAP decomposition residues, whereas the NH4-N removal efficiency without addition of HCl was only 96.4%. Moreover, the residual PO4-P from the end of reaction was recovered and the optimum recovery efficiency was achieved at a Mg:P molar ratio=6 and pH=10. Under these optimum conditions, the residual NH4-N and PO4-P concentrations in the treated wastewater, through 6 times of the recycling, were less than 15 mg/L and 1 mg/L, respectively. On the basis of this, an economic evaluation of the recycling MAP was made, and this recycle process could save 48.6% cost used in the chemicals for treating per cubic meter of the rare-earth wastewater, compared to the conventional MAP process.

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

    NARCIS (Netherlands)

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


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

  9. 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.


    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

  10. In Situ Detection of Chlorine Dioxide (C1O2) in the Radiolysis of Perchlorates and Implications for the Stability of Organics on Mars (United States)

    Góbi, Sándor; Bergantini, Alexandre; Kaiser, Ralf I.


    Magnesium perchlorate hexahydrate (Mg(ClO4)2 · 6H2O) samples were exposed to energetic electrons to investigate the products of the decomposition of perchlorates in the Martian soil and to infer their role in the degradation of organics on Mars. The samples were monitored online and in situ via infrared spectroscopy as well as electron impact (EI-QMS) and reflectron time-of-flight mass spectrometry coupled with single photon ionization (PI-ReTOF-MS). Our study reveals that besides chlorates ({{{ClO}}3}-) and molecular oxygen (O2), the chlorine dioxide radical (ClO2) was observed online and in situ for the first time as a radiolysis product of solid perchlorates. Chlorine dioxide, which is used on Earth as a strong oxidizing agent in water disinfection and bleaching, represents a proficient oxidizer—potentially more powerful than molecular oxygen—to explain the lack of abundant organics in the Martian soil.

  11. Crystal structure of (perchlorato-κO)(1,4,7,10-tetra-aza-cyclo-dodecane-κ(4)N)copper(II) perchlorate. (United States)

    Gray, Jessica L; Gerlach, Deidra L; Papish, Elizabeth T


    The crystal structure of the title salt, [Cu(ClO4)(C8H20N4)]ClO4, is reported. The Cu(II) ion exhibits a square-pyramidal geometry and is coordinated by the four N atoms of the neutral 1,4,7,10-tetra-aza-cyclo-dodecane (cyclen) ligand and an O atom from one perchlorate anion, with the second perchlorate ion hydrogen-bonded to one of the amine N atoms of the cyclen ligand. Additional N-H⋯O hydrogen bonds between the amine H atoms and the coordinating and non-coordinating perchlorate groups create a three-dimensional network structure. Crystals were grown from a concentrated methanol solution at ambient temperature, resulting in no co-crystallization of solvent.

  12. 21 CFR 520.310 - Caramiphen ethanedisulfonate and ammonium chloride tablets. (United States)


    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Caramiphen ethanedisulfonate and ammonium chloride... § 520.310 Caramiphen ethanedisulfonate and ammonium chloride tablets. (a) Specifications. Each tablet contains 10 milligrams of 5st caramiphen ethanedisulfonate and 80 milligrams of ammonium chloride.1 1...

  13. 40 CFR 415.240 - Applicability; description of the ammonium chloride production subcategory. (United States)


    ... ammonium chloride production subcategory. 415.240 Section 415.240 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Ammonium Chloride Production Subcategory § 415.240 Applicability; description of the ammonium chloride production subcategory. The provisions of this subpart are applicable to...

  14. 77 FR 21527 - Ammonium Nitrate From Russia: Correction to Notice of Opportunity To Request Administrative Review (United States)


    ... 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 5/2/2011-3... include the Ammonium Nitrate from Russia administrative review in the referenced notice. Dated: April...

  15. 77 FR 32669 - Ammonium Nitrate from Ukraine Institution of a Five-Year Review (United States)


    ... COMMISSION Ammonium Nitrate from Ukraine Institution of a Five-Year Review AGENCY: United States... determine whether revocation of the antidumping duty order on ammonium nitrate from Ukraine would be likely... ammonium nitrate from Ukraine (66 FR 47451). Following the five-year reviews by Commerce and the...

  16. Evaluation of perturbations in serum thyroid hormones during human pregnancy due to dietary iodide and perchlorate exposure using a biologically based dose-response model. (United States)

    Lumen, Annie; Mattie, David R; Fisher, Jeffrey W


    A biologically based dose-response model (BBDR) for the hypothalamic pituitary thyroid (HPT) axis was developed in the near-term pregnant mother and fetus. This model was calibrated to predict serum levels of iodide, total thyroxine (T4), free thyroxine (fT4), and total triiodothyronine (T3) in the mother and fetus for a range of dietary iodide intake. The model was extended to describe perchlorate, an environmental and food contaminant, that competes with the sodium iodide symporter protein for thyroidal uptake of iodide. Using this mode-of-action framework, simulations were performed to determine the daily ingestion rates of perchlorate that would be associated with hypothyroxinemia or onset of hypothyroidism for varying iodide intake. Model simulations suggested that a maternal iodide intake of 75 to 250 µg/day and an environmentally relevant exposure of perchlorate (~0.1 µg/kg/day) did not result in hypothyroxinemia or hypothyroidism. For a daily iodide-sufficient intake of 200 µg/day, the dose of perchlorate required to reduce maternal fT4 levels to a hypothyroxinemic state was estimated at 32.2 µg/kg/day. As iodide intake was lowered to 75 µg/day, the model simulated daily perchlorate dose required to cause hypothyroxinemia was reduced by eightfold. Similarly, the perchlorate intake rates associated with the onset of subclinical hypothyroidism ranged from 54.8 to 21.5 µg/kg/day for daily iodide intake of 250-75 µg/day. This BBDR-HPT axis model for pregnancy provides an example of a novel public health assessment tool that may be expanded to address other endocrine-active chemicals found in food and the environment.

  17. Perchlorate and volatiles of the brine of Lake Vida (Antarctica): Implication for the in situ analysis of Mars sediments (United States)

    Kenig, Fabien; Chou, Luoth; McKay, Christopher P.; Jackson, W. Andrew; Doran, Peter T.; Murray, Alison E.; Fritsen, Christian H.


    The cold (-13.4°C), cryoencapsulated, anoxic, interstitial brine of the >27 m thick ice of Lake Vida (Victoria Valley, Antarctica) contains 49 µg · L-1 of perchlorate and 11 µg · L-1 of chlorate. Lake Vida brine (LVBr) may provide an analog for potential oxychlorine-rich subsurface brine on Mars. LVBr volatiles were analyzed by solid-phase microextraction (SPME) gas chromatography-mass spectrometry (GC-MS) with two different SPME fibers. With the exception of volatile organic sulfur compounds, most other volatiles observed were artifacts produced in the GC injector when the thermal decomposition products of oxychlorines reacted with reduced carbon derived from LVBr and the SPME fiber phases. Analysis of MilliQ water with perchlorate (40 µg · L-1) showed low level of organic artifacts, reflecting carbon limitation. In order to observe sample-derived organic compounds, both in analog samples and on Mars, the molar abundance of reduced carbon in a sample must exceed those of O2 and Cl2 produced during decomposition of oxychlorines. This suggests that the abundance of compounds observed by the Sample Analysis at Mars (SAM) instruments in Sheepbed samples (CB-3, CB5, and CB6) may be controlled by an increase in the reduced-carbon/oxychlorine ratio of these samples. To increase chances of in situ detection of Martian organics during pyrolysis-GC-MS, we propose that the derivatization agents stored on SAM may be used as an external source of reduced carbon, increasing artificially the reduced-carbon to perchlorate ratio during pyrolysis, allowing the expression of more abundant and perhaps more diverse Martian organic matter.

  18. Perchlorate and Volatiles of the Brine of Lake Vida (Antarctica): Implication for the in Situ Analysis of Mars Sediments (United States)

    Kenig, Fabien; Chou, Luoth; McKay, Christopher P.; Jackson, W. Andrew; Doran, Peter T.; Murray, Alison E.; Fritsen, Christian H.


    The cold (-13.4 C), cryoencapsulated, anoxic, interstitial brine of the 27 m-thick ice of Lake Vida (Victoria Valley, Antarctica) contains 49 microgram L-1 of perchlorate and 11 microgram L-1 of chlorate. Lake Vida brine (LVBr) may provide an analog for potential oxychlorine-rich subsurface brine on Mars. LVBr volatiles were analyzed by solid-phase microextraction (SPME) gas chromatography-mass spectrometry (GC-MS) with two different SPME fibers. With the exception of volatile organic sulfur compounds, most other volatiles observed were artifacts produced in the GC injector when the thermal decomposition products of oxychlorines reacted with reduced carbon derived from LVBr and the SPME fiber phases. Analysis of MilliQ water with perchlorate (40 microgram L-1) showed low level of organic artifacts, reflecting carbon limitation. In order to observe sample-derived organic compounds, both in analog samples and on Mars, the molar abundance of reduced carbon in a sample must exceed those of O2 and Cl2 produced during decomposition of oxychlorines. This suggests that the abundance of compounds observed by the Sample Analysis at Mars (SAM) instruments in Sheepbed samples (CB-3, CB5, and CB6) may be controlled by an increase in the reduced-carbon/oxychlorine ratio of these samples. To increase chances of in situ detection of Martian organics during pyrolysis-GC-MS, we propose that the derivatization agents stored on SAM may be used as an external source of reduced carbon, increasing artificially the reduced-carbon to perchlorate ratio during pyrolysis, allowing the expression of more abundant and perhaps more diverse Martian organic matter.

  19. Effects of the anti-thyroidal compound potassium-perchlorate on the thyroid system of the zebrafish

    Energy Technology Data Exchange (ETDEWEB)

    Schmidt, Florian, E-mail: [Aquatic Ecology and Toxicology Group, Centre for Organismal Studies, University of Heidelberg, Im Neuenheimer Feld 230, D-69120 Heidelberg (Germany); Schnurr, Sarah; Wolf, Raoul; Braunbeck, Thomas [Aquatic Ecology and Toxicology Group, Centre for Organismal Studies, University of Heidelberg, Im Neuenheimer Feld 230, D-69120 Heidelberg (Germany)


    The increasing pollution of aquatic habitats with anthropogenic compounds has led to various test strategies to detect hazardous chemicals. However, information on effects of pollutants in the thyroid system in fish, which is essential for growth, development and parts of reproduction, is still scarce. Other vertebrate groups such as amphibians or mammals are well-studied; so the need for further knowledge especially in fish as a favored vertebrate model test organism is evident. Modified early life-stage tests were carried out with zebrafish exposed to the known thyroid inhibitor potassium perchlorate (0, 62.5, 125, 250, 500 and 5000 {mu}g/L) to identify adverse effects on the hypothalamic-pituitary-thyroid axis. Especially higher perchlorate concentrations led to conspicuous alterations in thyroidal tissue architecture and to effects in the pituitary. In the thyroid, severe hyperplasia at concentrations {>=}500 {mu}g/L together with an increase in follicle number could be detected. The most sensitive endpoint was the colloid, which showed alterations at {>=}250 {mu}g/L. The tinctorial properties and the texture of the colloid changed dramatically. Interestingly, effects on epithelial cell height were minor. The pituitary revealed significant proliferations of TSH-producing cells resulting in alterations in the ratio of adeno- to neurohypophysis. The liver as the main site of T4 deiodination showed severe glycogen depletion at concentrations {>=}250 {mu}g/L. In summary, the thyroid system in zebrafish showed effects by perchlorate from concentrations {>=}250 {mu}g/L, thus documenting a high sensitivity of the zebrafish thyroid gland for goitrogens. In the future, such distinct alterations could lead to a better understanding and identification of potential thyroid-disrupting chemicals.

  20. Systematic evaluation of nitrate and perchlorate bioreduction kinetics in groundwater using a hydrogen-based membrane biofilm reactor. (United States)

    Ziv-El, Michal C; Rittmann, Bruce E


    To evaluate the simultaneous reduction kinetics of the oxidized compounds, we treated nitrate-contaminated groundwater (approximately 9.4 mg-N/L) containing low concentrations of perchlorate (approximately 12.5 microg/L) and saturated with dissolved oxygen (approximately 8 mg/L) in a hydrogen-based membrane biofilm reactor (MBfR). We systematically increased the hydrogen availability and simultaneously varied the surface loading of the oxidized compounds on the biofilm in order to provide a comprehensive, quantitative data set with which to evaluate the relationship between electron donor (H(2)) availability, surface loading of the electron acceptors (oxidized compounds), and simultaneous bioreduction of the electron acceptors. Increasing the H(2) pressure delivered more H(2) gas, and the total H(2) flux increased linearly from approximately 0.04 mg/cm(2)-d for 0.5 psig (0.034 atm) to 0.13 mg/cm(2)-d for 9.5 psig (0.65 atm). This increased rate of H(2) delivery allowed for continued reduction of the acceptors as their surface loading increased. The electron acceptors had a clear hydrogen-utilization order when the availability of hydrogen was limited: oxygen, nitrate, nitrite, and then perchlorate. Spiking the influent with perchlorate or nitrate allowed us to identify the maximum surface loadings that still achieved more than 99.5% reduction of both oxidized contaminants: 0.21 mg NO(3)-N/cm(2)-d and 3.4 microg ClO(4)/cm(2)-d. Both maximum values appear to be controlled by factors other than hydrogen availability.

  1. 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


    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

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

    Directory of Open Access Journals (Sweden)

    Loussouarn C.


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

  3. cis-Aquabis(2,2′-bipyridine-κ2N,N′fluoridochromium(III bis(perchlorate dihydrate

    Directory of Open Access Journals (Sweden)

    Torben Birk


    Full Text Available The title mixed aqua–fluoride complex, [CrF(C10H8N22(H2O](ClO42·2H2O, has been synthesized by aquation of the corresponding difluoride complex using lanthanide(III ions as F− acceptors. The complex crystallizes with a CrIII ion at the center of a distorted octahedral coordination polyhedron with a cis arrangement of ligands. The crystal packing shows a hydrogen-bonding pattern involving water molecules, the coordinated F atom and the perchlorate anions

  4. Kinetics and mechanism of oxidation of glycine by iron(III)-1,10-phenanthroline complex in perchloric acid medium

    Indian Academy of Sciences (India)

    T V N Partha Sarathi; A Kalyan Kumar; K Krishna Kishore; P Vani


    Kinetics and mechanism of oxidation of glycine by iron(III)-1,10-phenanthroline complex has been studied in perchloric acid medium. The reaction is first order with respect to iron(III) and glycine. An increase in (phenanthroline) increases the rate, while increase in [H+] decreases the rate. Hence it can be inferred that the reactive species of the substrate is the zwitterionic form and that of the oxidant is [Fe(phen)2(H2O)2]3+. The proposed mechanism leads to the rate law as elucidated.

  5. The Preparation and Structure of [(2,4-Dimethyl-8-ethyl-5,8-diazadec-4-ene-2-aminechlorocopper(II] Perchlorate

    Directory of Open Access Journals (Sweden)

    Neil F. Curtis


    Full Text Available Copper(II chloride and perchlorate, N,N-diethylethane-1,2-diamine, react in (methanol with acetone and ammonia to form [(2,4-dimethyl-8-ethyl-5,8-diazadec-4-ene-2-aminechlorocopper(II] perchlorate, C12H27Cl2CuN3O4, , monoclinic, C2/c, (Hall-C2/c; a, 26.418(1, b, 9.7385(4; c, 14.0993(5 Å; β, 91.134(3°. This has copper(II in tetrahedrally distorted square-planar coordination by one primary, one tertiary, and one imine nitrogen atom and the chloride ion.

  6. catena-Poly[[[(dimethyl-malonato-κO:O')(perchlorato-κO)copper(II)]-μ-bis-(3-pyridylmeth-yl)piperazinediium-κN:N] perchlorate dihydrate]. (United States)

    Farnum, Gregory A; Laduca, Robert L


    In the title compound, {[Cu(C(5)H(6)O(4))(ClO(4))(C(16)H(22)N(4))]ClO(4)·2H(2)O}(n), square-pyramidally coordinated Cu atoms with perchlorate and dimethyl-malonate ligands are connected into cationic sinusoidal coordination polymer chains by doubly protonated bis-(3-pyridylmeth-yl)piperazine (3-bpmp) ligands. The chains aggregate into pseudo-layers parallel to the (101) crystal planes by N-H⋯O hydrogen bonding. Unligated perchlorate anions and water mol-ecules of crystallization provide additional hydrogen bonding between pseudo-layers.

  7. Solution-reaction Calorimetric Study of Coordination Compounds of Rare Earth Perchlorates with Alanine and Imidazole

    Institute of Scientific and Technical Information of China (English)

    ZHAO, Yan-Ru(赵艳茹); HOU, An-Xin(侯安新); DONG, Jia-Xin(董家新); ZHAO, Shun-Sheng(赵顺省); LIU, Yi(刘义); QU, Song-Sheng(屈松生)


    Two coordination compounds of rare earth perchlorates with alanine and imidazole, [RE(Ala)n(Im)(H2O)](ClO4)3(s) (RE=La, n=3; RE=Nd, n=2), have been prepared and characterized. The standard molar enthalpies of reaction for the following two reactions, LaCL·7H2O(s)+3Ala(s)+Im(s)+3NaClO4(s)=[La(Ala).(Im)(H2O)]-(ClO4)3(s)+3NaCl(s)+6H2O(I)(1)and NdCl3·6H2O(s)+2Ala(s)+2Ala(s)+Im(s)+3NaClO4(s)=[Nd(Ala)2(Im)(H2O)]-(ClO4)3(s)+3NaCl(s)+5H2O(l) (2), were determined by solution-reaction calorimetry, at T=298.15 K, as 36.168 ±0.642kJ·mol-1 and 48.590±0.934kJ·mol-1 respectively. From the results and other auxiliary quantities, the standard molar enthalpies of formation of [La(Ala)3(Im)(H2O)](ClO4)3(s) and [Nd(Ala)2(Im)(H2O)] (ClO4)3(s) were derived,△fH(-)m{[La(Ala).(Im)(H2O)](ClO4)3,s}=(-2984.8±1.0)kJ·mol-1 and △fH(-)m{[Nd(Ala).(Im)(H2O)]-(ClO4)3,s}=(-2387.8±0.8)kJ·mol-1, respectively.

  8. Dracorhodin Perchlorate Induced Human Breast Cancer MCF-7 Apoptosis through Mitochondrial Pathways (United States)

    Yu, Jing-hua; Zheng, Gui-bin; Liu, Chun-yu; Zhang, Li-ying; Gao, Hong-mei; Zhang, Ya-hong; Dai, Chun-yan; Huang, Lin; Meng, Xian-ying; Zhang, Wen-yan; Yu, Xiao-fang


    Objective: Dracorhodin perchlorate (DP) was a synthetic analogue of the antimicrobial anthocyanin red pigment dracorhodin. It was reported that DP could induce apoptosis in human prostate cancer, human gastric tumor cells and human melanoma, but the cytotoxic effect of DP on human breast cancer was not investigated. This study would investigate whether DP was a candidate chemical of anti-human breast cancer. Methods: The MTT assay reflected the number of viable cells through measuring the activity of cellular enzymes. Phase contrast microscopy visualized cell morphology. Fluorescence microscopy detected nuclear fragmentation after Hoechst 33258 staining. Flowcytometric analysis of Annexin V-PI staining and Rodamine 123 staining was used to detect cell apoptosis and mitochondrial membrane potential (MMP). Real time PCR detected mRNA level. Western blot examined protein expression. Results: DP dose and time-dependently inhibited the growth of MCF-7 cells. DP inhibited MCF-7 cell growth through apoptosis. DP regulated the expression of Bcl-2 and Bax, which were mitochondrial pathway proteins, to decrease MMP, and DP promoted the transcription of Bax and inhibited Bcl-2. Apoptosis-inducing factor (AIF) and cytochrome c which localized in mitochondrial in physiological condition were released into cytoplasm when MMP was decreased. DP activated caspase-9, which was the downstream of mitochondrial pathway. Therefore DP decreased MMP to release AIF and cytochrome c into cytoplasm, further activating caspase 9, lastly led to apoptosis. Conclusion: Therefore DP was a candidate for anti-breast cancer, DP induced apoptosis of MCF-7 through mitochondrial pathway. PMID:23869191

  9. Widespread presence of naturally occurring perchlorate in high plains of Texas and New Mexico. (United States)

    Rajagopalan, Srinath; Anderson, Todd A; Fahlquist, Lynne; Rainwater, Ken A; Ridley, Moira; Jackson, W Andrew


    Perchlorate (CLO4-) occurrence in groundwater has previously been linked to industrial releases and the historic use of Chilean nitrate fertilizers. However, recently a number of occurrences have been identified for which there is no obvious anthropogenic source. Groundwater from an area of 155,000 km2 in 56 counties in northwest Texas and eastern New Mexico is impacted bythe presence of ClO4-. Concentrations were generally low (areas are impacted by concentrations up to 200 ppb. ClO4- distribution is not related to well type (public water system, domestic, agricultural, or water-table monitoring) or aquifer (Ogallala, Edward Trinity High Plains, Edwards Trinity Plateau, Seymour, or Cenozoic). Results from vertically nested wells strongly indicate a surface source. The source of ClO4- appears to most likely be atmospheric deposition. Evidence supporting this hypothesis primarily relates to the presence of ClO4- in tritium-free older water, the lack of relation between land use and concentration distribution, the inability of potential anthropogenic sources to account for the estimated mass of ClO4-, and the positive relationship between conserved anions (e.g., IO3-, Cl-, SO4(-2)) and ClO4-. The ClO4- distribution appears to be mainly related to evaporative concentration and unsaturated transport. This process has led to higher ClO4- and other ion concentrations in groundwater where the water table is relatively shallow, and in areas with lower saturated thickness. Irrigation may have accelerated this process in some areas by increasing the transport of accumulated salts and by increasing the number of evaporative cycles. Results from this study highlight the potential for ClO4- to impact groundwater in arid and semi-arid areas through long-term atmospheric deposition.

  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


    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. Thorium adsorption behaviour on mixed ammonium lanthanum oxalate, LAOX

    Energy Technology Data Exchange (ETDEWEB)

    Valentini Ganzerli, M.T.; Maggi, L.; Crespi Caramella, V


    The cation-exchange properties of mixed ammonium lanthanum oxalate, LAOX, were studied by batch equilibration as a function of the concentration of some cations, such as alkaline earths or ammonium and of some anions and acids. The distribution coefficients for thorium are high, while U(VI) is not adsorbed over a large acidity range. Thus, the separation of thorium from uranium may be successfully carried out. The experimental conditions of adsorption, elution and recovery of thorium were investigated as well, by using chromatographic columns filled with LAOX, in order to set best the separation conditions from uranyl ions. Instrumental neutron activation analysis, ICP emission spectrometry and the UV spectrometry were used to evaluate the thorium, uranium and lanthanum concentrations00.

  12. Thermal stability assessment of anti-explosive ammonium nitrate

    Institute of Scientific and Technical Information of China (English)

    Lijin Shen; Xuguang Wang


    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. Anaerobic ammonium oxidation in a bioreactor treating slaughterhouse wastewater

    Directory of Open Access Journals (Sweden)

    V. Reginatto


    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.

  14. Preparation of nanodispersed titania using stabilized ammonium nitrate melts

    KAUST Repository

    Raciulete, Monica


    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.

  15. The nitrogen Sternheimer antishielding factor in the ammonium ion (United States)

    Fowler, P. W.; Kelly, H. M.; Brown, R. J. C.


    Coupled Hartree-Fock calculations in various basis sets yield values in the range 6.7 to 6.8 for the Sternheimer antishielding factor (1 - γ ∞) of the nitrogen nucleus in the ammonium ion. These are in substantial agreement with the value of 9 that is obtained from a model of measured relaxation times in solid ammonium chloride when allowance is made for effects of the crystalline environment on the chloride ion Sternheimer antishielding factor. Other experimental estimates of the nitrogen Sternheimer factor are discussed. The new value is used to derive cation field gradients from measured quadrupole coupling constants in solid NH 4ReO 4 and NH 4IO 4.

  16. Ammonium sulphate precipitation overestimates titres of anti-peptide antisera. (United States)

    Roth, B; Barkas, T


    Precipitation by 50% final saturation of ammonium sulphate, a method commonly used to estimate titres and affinity constants of antibodies, was found consistently to overestimate the titre of anti-peptide antisera when compared with other antibody precipitants. The effect could not be attributed to non-IgG fractions, and similar overestimations were found when pure IgG was used. We suggest that the lower values represent a more physiologically relevant estimation.

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

    Institute of Scientific and Technical Information of China (English)


    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.

  18. Ammonium photo-production by heterocytous cyanobacteria: potentials and constraints. (United States)

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


    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.

  19. Proton- and ammonium- sensing by histaminergic neurons controlling wakefulness.

    Directory of Open Access Journals (Sweden)

    Yvgenij eYanovsky


    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.

  20. Nanomodified vermiculite NMV - a new material for recycling ammonium nitrogen (United States)

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


    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.

  1. Structural basis for Mep2 ammonium transceptor activation by phosphorylation. (United States)

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


    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.

  2. Removal of chloridazon by natural and ammonium kerolite samples (United States)

    Socías-Viciana, M. M.; Tévar de Fez, J.; Ureña-Amate, M. D.; González-Pradas, E.; Fernández-Pérez, M.; Flores-Céspedes, F.


    The adsorption of chloridazon (5-amino-4-chloro-2-phenylpyridazin-3(2H)-one) on natural and ammonium kerolite samples from aqueous solution at 10, 25 and 40 °C has been studied by using batch experiments. The experimental data points were fitted to the Langmuir equation in order to calculate the adsorption capacities ( Xm) of the samples; two straight lines were obtained, which indicates that the adsorption process takes place in two different stages. Values for Xm1 (first stage) ranged from 1.1 × 10 -2 mol kg -1 for natural kerolite at 40 °C up to 5.1 × 10 -2 mol kg -1 for ammonium kerolite at 10 °C and the values for Xm2 (second stage) ranged from 9.1 × 10 -2 mol kg -1 for natural kerolite at 40 °C up to 14 × 10 -2 mol kg -1 for natural kerolite at 10 °C. The adsorption experiments showed on the one hand, that the ammonium kerolite is more effective than natural kerolite to adsorb chloridazon in the range of temperature studied and on the other hand, that the lower temperature, the more effective the adsorption of chloridazon on the adsorbents studied.

  3. Extraction Factor Of Pure Ammonium Paratungstate From Tungsten Scraps

    Directory of Open Access Journals (Sweden)

    Pee J.-H.


    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.

  4. Ammonium nitrogen in fetuses of urea-treated sheep. (United States)

    Yelverton, C C; Roller, M H; Swanson, R N


    Eight pregnant Southdown ewes were treated (by drench) with 12.5 ml of 3.3 M urea solution per kilogram of body weight, and ammonium nitrogen concentrations of blood and tissues of these ewes and their fetuses were measured and compared with those of control ewes (given water by drench) and their fetuses. Blood ammonium nitrogen (BAN) and tissue ammonium nitrogen (TAN) concentrations for liver, kidney, spleen, and muscle of ewes and fetuses were determined by an ion-exchange procedure. Samples of blood were collected before treatment, at 30, 90 and 150 minutes after treatment, and at death of the dam. The principal ewes had increasing BAN concentrations with time after drench, and their fetuses had significantly greater (P less than 0.01) BAN concentrations than fetuses from control ewes. All fetuses were alive after death of the dams and had lower TAN values than their dams. The differences in ammonia concentrations between ewes and fetuses were larger in the principal group than in the control group. Except for ewe muscle and fetal liver, all tissues of principals had significantly greater (P less than 0.01) TAN concentrations than those of controls. Muscle of principal ewes and hepatic tissues of their fetuses had greater (P less than 0.05) TAN concentrations than those of control ewes and their fetuses.

  5. Quaternary ammonium salt N-(dodecyloxycarboxymethyl)-N,N,N-trimethyl ammonium chloride induced alterations in Saccharomyces cerevisiae physiology

    Indian Academy of Sciences (India)



    We investigated the influence of the quaternary ammonium salt (QAS) called IM (N-(dodecyloxycarboxymethyl)-N,N,N-trimethyl ammonium chloride) on yeast cells of the parental strain and the IM-resistant mutant (EO25 IMR)growth. The phenotype of this mutant was pleiotropic. The IMR mutant exhibited resistance to ethanol, osmotic shockand oxidative stress, as well as increased sensitivity to UV. Moreover, it was noted that mutant EO25 appears to havean increased resistance to clotrimazole, ketoconazole, fluconazole, nystatin and cycloheximide. It also toleratedgrowth in the presence of crystal violet, DTT and metals (selenium, tin, arsenic). It was shown that the presence ofIM decreased ergosterol level in mutant plasma membrane and increased its unsaturation. These results indicatechanges in the cell lipid composition. Western blot analysis showed the induction of Pma1 level by IM. RT-PCRrevealed an increased PMA1 expression after IM treatment.

  6. Evidence for surface nucleation: efflorescence of ammonium sulfate and coated ammonium sulfate aerosol particles (United States)

    Ciobanu, V. Gabriela; Marcolli, Claudia; Krieger, Ulrich K.; Zuend, Andreas; Peter, Thomas


    Aerosol particles are ubiquitous in the atmosphere and can undergo different phase transitions, such as deliquescence and efflorescence. Using optical microscopy, we investigated the efflorescence of ammonium sulfate (AS) in supersaturated AS and 1:1 and 8:1 (by weight) poly(ethylene glycol)-400 (PEG-400)/AS particles, which were deposited as droplets with diameters in the 16 - 35 μm range on a hydrophobically coated slide. The PEG-400/AS particles that are exposed to decreasing relative humidity (RH) exhibit a liquid-liquid phase separation below 90 % RH with the PEG-400 phase surrounding the aqueous AS inner phase (Marcolli and Krieger, 2006; Ciobanu et al., 2009). Pure AS particles effloresced in the RH range from 36.3 to 43.7 % RH, in agreement with literature data (31 - 48 % RH). In contrast, 1:1 PEG-400/AS particles with diameters of the AS phase from 7.2 - 19.2 μm effloresced between 26.8 - 33.9 % RH and 8:1 PEG-400/AS particles with diameters of the AS phase from 1.8 - 7.3 μm between 24.3 - 29.3 % RH. Such low efflorescence relative humidity (ERH) values have never been reached before for AS particles of this size range. We show that neither a potential inhibition of water evaporation via anomalously slow diffusion through the PEG coating, nor the presence of low amounts of PEG-400 in the AS phase, nor different timescales between various experimental techniques could possibly explain the low AS ERH values of PEG-400/AS particles in our setup. High-speed photography of the efflorescence process allowed to monitor the proceeding of the AS crystallization fronts within the particles with millisecond time resolution. The nucleation locations were deduced based on the initial crystals growth locations. Statistical analysis of 31 and 19 efflorescence events for pure AS and 1:1 PEG-400/AS particles, respectively, identified the air/droplet/substrate contact line and the air/droplet interface as preferred nucleation locations in the case of pure AS particles

  7. Evidence for perchlorates and the origin of chlorinated hydrocarbons detected by SAM at the Rocknest aeolian deposit in Gale Crater (United States)

    Glavin, Daniel P.; Freissinet, Caroline; Miller, Kristen E.; Eigenbrode, Jennifer L.; Brunner, Anna E.; Buch, Arnaud; Sutter, Brad; Archer, P. Douglas; Atreya, Sushil K.; Brinckerhoff, William B.; Cabane, Michel; Coll, Patrice; Conrad, Pamela G.; Coscia, David; Dworkin, Jason P.; Franz, Heather B.; Grotzinger, John P.; Leshin, Laurie A.; Martin, Mildred G.; McKay, Christopher; Ming, Douglas W.; Navarro-González, Rafael; Pavlov, Alexander; Steele, Andrew; Summons, Roger E.; Szopa, Cyril; Teinturier, Samuel; Mahaffy, Paul R.


    A single scoop of the Rocknest aeolian deposit was sieved (trichloromethane, a chloromethylpropene, and chlorobenzene were identified by SAM above background levels with abundances of ~0.01 to 2.3 nmol. The evolution of the chloromethanes observed during pyrolysis is coincident with the increase in O2 released from the Rocknest sample and the decomposition of a product of N-methyl-N-(tert-butyldimethylsilyl)-trifluoroacetamide (MTBSTFA), a chemical whose vapors were released from a derivatization cup inside SAM. The best candidate for the oxychlorine compounds in Rocknest is a hydrated calcium perchlorate (Ca(ClO4)2·nH2O), based on the temperature release of O2 that correlates with the release of the chlorinated hydrocarbons measured by SAM, although other chlorine-bearing phases are being considered. Laboratory analog experiments suggest that the reaction of Martian chlorine from perchlorate decomposition with terrestrial organic carbon from MTBSTFA during pyrolysis can explain the presence of three chloromethanes and a chloromethylpropene detected by SAM. Chlorobenzene may be attributed to reactions of Martian chlorine released during pyrolysis with terrestrial benzene or toluene derived from 2,6-diphenylphenylene oxide (Tenax) on the SAM hydrocarbon trap. At this time we do not have definitive evidence to support a nonterrestrial carbon source for these chlorinated hydrocarbons, nor do we exclude the possibility that future SAM analyses will reveal the presence of organic compounds native to the Martian regolith.

  8. Study of the ion-channel behavior on glassy carbon electrode supported bilayer lipid membranes stimulated by perchlorate anion

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Zhiquan; Shi, Jun; Huang, Weimin, E-mail:


    In this paper, a kind of didodecyldimethylammonium bromide (DDAB) layer membranes was supported on a glassy carbon electrode (GCE). We studied the ion channel behavior of the supported bilayer lipid membrane by scanning electrochemical microscopy (SCEM) in tris(2,2′-bipyridine) ruthenium(II) solution. Perchlorate anion was used as a presence of stimulus and ruthenium(II) complex cations as the probing ions for the measurement of SECM, the lipid membrane channel was opened and exhibited the behavior of distinct SECM positive feedback curve. The channel was in a closed state in the absence of perchlorate anions while reflected the behavior of SECM negative feedback curve. The rates of electron transfer reaction in the lipid membranes surface were detected and it was dependant on the potential of SECM. - Highlights: • The rates of electron transfer reaction in the lipid membranes surface were detected. • Dynamic investigations of ion-channel behavior of supported bilayer lipid membranes by scanning electrochemical microscopy • A novel way to explore the interaction between molecules and supported bilayer lipid membranes.

  9. Crystal structure of barium perchlorate anhydrate, Ba(ClO42, from laboratory X-ray powder data

    Directory of Open Access Journals (Sweden)

    Jeonghoo H. Lee


    Full Text Available The previously unknown crystal structure of barium perchlorate anhydrate, determined and refined from laboratory X-ray powder diffraction data, represents a new structure type. The title compound was obtained by heating hydrated barium perchlorate [Ba(ClO42·xH2O] at 423 K in vacuo for 6 h. It crystallizes in the orthorhombic space group Fddd. The asymmetric unit contains one Ba (site symmetry 222 on special position 8a, one Cl (site symmetry 2 on special position 16f and two O sites (on general positions 32h. The structure can be described as a three-dimensional polyhedral network resulting from the corner- and edge-sharing of BaO12 polyhedra and ClO4 tetrahedra. Each BaO12 polyhedron shares corners with eight ClO4 tetrahedra, and edges with two ClO4 tetrahedra. Each ClO4 tetrahedron shares corners with four BaO12 polyhedra, and an edge with the other BaO12 polyhedron.

  10. Analysis of Mixed Aryl/Alkyl Esters by Pyrolysis Gas Chromatography-Mass Spectrometry in the Presence of Perchlorate (United States)

    Burton, A. S.; Locke, D. R.; Lewis, E. K.


    Mars is an important target for Astrobiology. A key goal of the MSL mission was to determine whether Mars was habitable in the past, a que-tion that has now been definitely determined to be yes. Another key goal for Mars exploration is to understand the origin and distribution of organic material on Mars; this question is being addressed by the SAM instrument on MSL, and will also be informed by two upcoming Mars exploration missions, ExoMars and Mars 2020. These latter two missions have instrumentation capable of detecting and characterize organic molecules. Over the next decade, these missions will analyze organics in surface, near-surface and sub-surface samples. Each mission has the capability to analyze organics by different methods (pyrolysis gas chromatography-mass spectrometry [py-GC-MS]; laser desorption and thermal volatilization GC-MS; and Raman spectroscopy). Plausibly extraterrestrial organics were recently discovered by the Mars Science Laboratory (MSL), providing an important first step towards understanding the organic inventory on Mars [1]. The compounds detected were chlorobenzenes and chloroalkanes, but it was argued that chlorination of these compounds occurred during pyrolysis of samples containing unchlorinated organics in the presence of perchlorate. A recent report analyzed a suite of aromatic (benzene, toluene, benzoic acid, phthalic acid, and mellitic acid) and aliphatic (acetic acid, propane, propanol, and hexane) by pyrolysis under SAM-like conditions in the presence of perchlorate to attempt to constrain possible precursor molecules for the organic molecules detected on Mars. For aromatic compounds, the aromatic acids all readily produced SAM-relevant chlorobenzes, whereas benzene and toluene did not. This observation suggests that the chlorobenzene detected on Mars could have derived from compounds like mellitic acid, consistent with the previous hypothesis by Benner et al. [3]. Among the aliphatic molecules, it was shown that

  11. Ferric Perchlorate Catalyzed One-pot Synthesis of 1,2,3,4-Tetrahydro-2-pyrimidinones and -thiones:an Expedient Protocol for the Biginelli Reaction

    Institute of Scientific and Technical Information of China (English)

    HERAVI,Majid Momahed; BEHBAHANI,Farahnaz Kargar OSKOOIE; Hossien Abdi


    An efficient synthesis of 1,2,3,4-tetrahydro-2-pyrimidinones and -thiones using ferric perchlorate as the catalyst from an aldehyde, ethyl acetoacetate, and urea or thiourea in acetonitrile was described. Compared to the classical Biginelli reaction conditions, this new method consistently has the advantage of full catalysis, good yields and short reaction time.

  12. Comparing the removal of perchlorate when using single-walled carbon nanotubes (SWCNTs) or granular activated carbon: adsorption kinetics and thermodynamics. (United States)

    Lou, Jie C; Hsu, Yung S; Hsu, Kai L; Chou, Ming S; Han, Jia Y


    This study aims to remove perchlorate using single-walled carbon nanotubes (SWCNTs) or granular activated carbon (GAC). Dynamic and equilibrium adsorption experiments were performed to evaluate the thermodynamic behavior of perchlorate on SWCNTs and GAC. Key parameters affecting the adsorption, such as pH, ionic strength, and temperature were studied. The experimental results showed that the dynamic adsorption experiment achieved equilibrium in approximately eight hours. The adsorption capacity increased as the concentration of perchlorate increased or as the ionic strength decreased. The selected adsorption models were the modified Freundlich, the pseudo-1st-order, and the pseudo-2nd-order equations. The results showed that the modified Freundlich equation best described the kinetic adsorption processes. The maximal adsorption capacities of GAC and SWCNTs were 33.87-28.21 mg/g and 13.64 - 10.03 mg/g, respectively, at a constant temperature between 5°C and 45°C. The thermodynamic parameters, such as the equilibrium constant (K0 ), the standard free energy changes (ΔG°), the standard enthalpy change (ΔH°) and the standard entropy change (ΔS°), were obtained. The results of the isothermal equilibrium adsorption experiment showed that low pH levels, low ionic strength, and low-temperature conditions facilitated the perchlorate adsorption, indicating that GAC and SWCNTs are potential absorbents for water treatment.


    NARCIS (Netherlands)



    Rate constants are reported for the solvolysis of p-nitrophenylsulfonylmethyl perchlorate in binary ethanolic and methanolic mixtures at 298.2 K. Co-solvents include hydrocarbons, chlorinated hydrocarbons and 1,4-dioxane. The kinetic data are examined in terms of the effect of decreasing mole fracti


    Perchlorate (ClO4) and 3,3',4,4',5-pentachlorobiphenyl (PCB126) are environmental contaminants known to disturb thyroid hormone homeostasis by well defined modes of action that lead to hypothyroidism in the rat. PCB126 increases phase II conjugation of T4 (T4-glucuronide) by indu...

  15. Selective Anion Exchange Resins for the Removal of Perchlorate [(CIO{sub 4}{sup -})] from Groundwater

    Energy Technology Data Exchange (ETDEWEB)

    Gu, B.


    The primary objective of this project was to evaluate a novel bifunctional anion exchange resin for the cost-effective, in situ treatment of groundwater contaminated with perchlorate (ClO{sub 4}{sup -}). Both laboratory and field studies were performed to determine the selectivity and capacity of the bifunctional synthetic resins to sorb ClO{sub 4}{sup -} from simulated or actual contaminated groundwater. A number of synthetic bifunctional resins, including two commercial versions made by Purolite International and three commercially available, mono-functional resins, were tested. Initial laboratory batch and column breakthrough studies determined the best synthetic resins and the optimal conditions for the field experiment. Laboratory results indicated that the bifunctional synthetic resins, D-3696 and RO-02-119 were highly selective toward ClO{sub 4}{sup -} and performed {approx}5 times better than the best commercial nitrate resin (Purolite{reg_sign} A-520E) and more than an order of magnitude better than some nonselective commercial resins (e.g. Amberlite{reg_sign} IRA-900). The bifunctional resins were particularly effective in removing trace quantities of ClO{sub 4}{sup -} in groundwater to below the detection limit ({approx} 3 {micro}g/L). A field trial demonstrated that the bifunctional resin (D-3696) was able to treat {approx} 110,000 bed volumes of groundwater before a 10% breakthrough of ClO{sub 4}{sup -} occurred under the column flow-through conditions (running at {approx} 2 bed volumes per minute). On the other hand, the Purolite{reg_sign} A-520E resin was able to treat {approx} 23,000 bed volumes of groundwater under the same experimental conditions. No pretreatment was needed to remove either dissolved organic matter or other competing anions (such as SO{sub 4}{sup 2-} or NO{sub 3}{sup -}) in the groundwater, and the treatment process did not alter the water quality by removing or adding secondary by-products because of the high selectivity of the

  16. Soil, plant, and terrain effects on natural perchlorate distribution in a desert landscape (United States)

    Andraski, Brian J.; Jackson, W.A.; Welborn, Toby L.; Böhlke, John Karl; Sevanthi, Ritesh; Stonestrom, David A.


    Perchlorate (ClO4−) is a contaminant that occurs naturally throughout the world, but little is known about its distribution and interactions in terrestrial ecosystems. The objectives of this Amargosa Desert, Nevada study were to determine (i) the local-scale distribution of shallow-soil (0–30 cm) ClO4− with respect to shrub proximity (far and near) in three geomorphic settings (shoulder slope, footslope, and valley floor); (ii) the importance of soil, plant, and terrain variables on the hillslope-distribution of shallow-soil and creosote bush [Larrea tridentata (Sessé & Moc. ex DC.) Coville] ClO4−; and (iii) atmospheric (wet plus dry, including dust) deposition of ClO4− in relation to soil and plant reservoirs and cycling. Soil ClO4− ranged from 0.3 to 5.0 μg kg−1. Within settings, valley floor ClO4− was 17× less near shrubs due in part to enhanced leaching, whereas shoulder and footslope values were ∼2× greater near shrubs. Hillslope regression models (soil, R2 = 0.42; leaf, R2 = 0.74) identified topographic and soil effects on ClO4− deposition, transport, and cycling. Selective plant uptake, bioaccumulation, and soil enrichment were evidenced by leaf ClO4− concentrations and Cl−/ClO4− molar ratios that were ∼8000× greater and 40× less, respectively, than soil values. Atmospheric deposition ClO4− flux was 343 mg ha−1 yr−1, ∼10× that for published southwestern wet-deposition fluxes. Creosote bush canopy ClO4− (1310 mg ha−1) was identified as a previously unrecognized but important and active reservoir. Nitrate δ18O analyses of atmospheric deposition and soil supported the leaf-cycled–ClO4− input hypothesis. This study provides basic data on ClO4− distribution and cycling that are pertinent to the assessment of environmental impacts in desert ecosystems and broadly transferable to anthropogenically contaminated systems.

  17. 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.


    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.

  18. Changes in gastric sodium-iodide symporter (NIS) activity are associated with differences in thyroid gland sensitivity to perchlorate during metamorphosis. (United States)

    Carr, James A; Murali, Sharanya; Hu, Fang; Goleman, Wanda L; Carr, Deborah L; Smith, Ernest E; Wages, Mike


    We investigated stage-dependent changes in sensitivity of the thyroid gland to perchlorate during development of African clawed frog tadpoles (Xenopus laevis) in relation to non-thyroidal iodide transporting tissues. Perchlorate-induced increases in thyroid follicle cell size and colloid depletion were blunted when exposures began at Nieuwkoop-Faber (NF) stage 55 compared to when exposures began at NF stages 49 or 1-10. To determine if the development of other iodide transporting tissues may contribute to this difference we first examined which tissues expressed transcripts for the sodium dependent iodide symporter (NIS). RT-PCR analysis revealed that NIS was expressed in stomach and small intestine in addition to the thyroid gland of X. laevis tadpoles. NIS mRNA was not detected in lung, kidney, skin, gill, muscle, heart or liver. Perchlorate sensitive (125)I uptake was found in stomach, lung, kidney, gill, and small intestine but not muscle, liver, or heart. Perchlorate-sensitive (125)I uptake by stomach was 6-10 times greater than in any other non-thyroidal tissue in tadpoles. While NF stage 49 tadpoles exhibited perchlorate-sensitive uptake in stomach it was roughly 4-fold less than that observed in NF stage 55 tadpoles. Although abundance of NIS gene transcripts was greater in stomachs from NF stage 55 compared to NF stage 49 tadpoles this difference was not statistically significant. We conclude that gastric iodide uptake increases between NF stages 49 and 55, possibly due to post-translational changes in NIS glycosylation or trafficking within gastric mucosal cells. These developmental changes in gastric NIS gene expression may affect iodide availability to the thyroid gland.

  19. The Properties of Ammonium Dinitramine (ADN): Part 2: Melt Casting (United States)

    Hahma, A.; Edvinsson, H.; Östmark, H.


    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.

  20. Surge ammonium uptake in macroalgae from a coral atoll

    Digital Repository Service at National Institute of Oceanography (India)

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

    Maintenance of high levels of biological productivity (up to several gC m-2 d-1) (Crossland et al., 1991) by coral atolls in oligotrophic oceanic waters with low ambient concentrations of N nutrients (typically of the order of few hundreds of nmols..., fish shoals migrating onto the reef could raise ambient ammonium concentrations in the vicinity of corals up to 0.9 ? M (Meyer et al., 1983) and area-specific N regeneration by actively feeding holothurians (Uthicke and Klumpp, 1998) could be in a...

  1. 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)


    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.

  2. Experimental study of the detonation of technical grade ammonium nitrate (United States)

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


    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).

  3. Ammonium diamminesilver(I bis(5-chloro-2-hydroxybenzenesulfonate trihydrate

    Directory of Open Access Journals (Sweden)

    Zhao-Peng Deng


    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.

  4. Theoretical Study of Energetic Complexes (Ⅲ): Bis-(5-nitro-2Htetrazolato-N2)tetraammine Cobalt(Ⅲ) Perchlorate (BNCP) and Its Transition Metal (Ni/Fe/Cu/Zn) Perchlorate Analogues

    Institute of Scientific and Technical Information of China (English)

    尚静; 张建国; 张同来; 黄辉胜; 张绍文; 舒远杰


    The geometric conformation and electronic structure of bis-(5-nitro-2H-tetrazolato-N2)tetraammine cobalt(Ⅲ) perchlorate and its Ni/Fe/Cu/Zn analogues are studied under the TPSS (Tao-Perdew-Staroverov-Scuseria) levels of density functional theory in order to throw light on the relationship between their energy gaps and impact sensitivity While the perchlorate ions are coordinated with the copper cation, which is different from the other four compounds NBO (Natural bond orbital) analyses indicated that the metal-ligand interaction in the Co complex is covalent, while the others are ionic. The analysis of the electrostatic potential demonstrated that the O atoms from the nitro-tetrazole ring and perchlorate were primarily negative, while the other atoms were positive. The study was also conducted to gain a better understanding of the correlation of the energy gap and impact sensitivity.

  5. Biological removal of selenate and ammonium by activated sludge in a sequencing batch reactor. (United States)

    Mal, J; Nancharaiah, Y V; van Hullebusch, E D; Lens, P N L


    Wastewaters contaminated by both selenium and ammonium need to be treated prior to discharge into natural water bodies, but there are no studies on the simultaneous removal of selenium and ammonium. A sequencing batch reactor (SBR) was inoculated with activated sludge and operated for 90days. The highest ammonium removal efficiency achieved was 98%, while the total nitrogen removal was 75%. Nearly a complete chemical oxygen demand removal efficiency was attained after 16days of operation, whereas complete selenate removal was achieved only after 66days. The highest total Se removal efficiency was 97%. Batch experiments showed that the total Se in the aqueous phase decreased by 21% with increasing initial ammonium concentration from 50 to 100mgL(-1). This study showed that SBR can remove both selenate and ammonium via, respectively, bioreduction and partial nitrification-denitrification and thus offer possibilities for treating selenium and ammonium contaminated effluents.

  6. Relations of ammonium minerals at several hydrothermal systems in the western U.S. (United States)

    Krohn, M. Dennis; Kendall, Carol; Evans, John R.; Fries, Terry L.


    Ammonium bound to silicate and sulfate minerals has recently been located at several major hydrothermal systems in the western U.S. utilizing newly-discovered near-infrared spectral properties. Knowledge of the origin and mineralogic relations of ammonium minerals at known hydrothermal systems is critical for the proper interpretation of remote sensing data and for testing of possible links to mineralization. Submicroscopic analysis of ammonium minerals from two mercury- and gold-bearing hot-springs deposits at Ivanhoe, Nevada and McLaughlin, California shows that the ammonium feldspar, buddingtonite, occurs as fine-grained euhedral crystals coating larger sulfide and quartz crystals. Ammonium feldspar seems to precipitate relatively late in the crystallization sequence and shows evidence for replacement of NH 4 + by K + or other monovalent cations. Some buddingtonite is observed in close association with mercury, but not with gold. Ammonioalunite is found in a variety of isolated crystal forms at both deposits. Nitrogen isotopic values for ammonium-bearing minerals show a 14‰ range in composition, precluding assignment of a specific provenance to the nitrogen. The correlations of nitrogen isotopic values with depth and ammonium content suggest some loss of nitrogen in the oxidizing supergene environment, possibly as a metastable mineral. The high ammonium content in these hydrothermal systems, the close association to mercury, and the small crystal size of the ammonium-bearing minerals all suggest that ammonium may be transported in a late-stage vapor phase or as an organic volatile. Such a process could lead to the formation of a non-carbonaceous organic aureole above a buried geothermal source. The discovery of a 10-km outcrop of ammonium minerals confirms that significant substitution of ammonium in minerals is possible over an extensive area and that remote sensing is a feasible means to detect such aureoles.

  7. Effects of Calcium Lignosulfonate and Silicic Acid on Ammonium Nitrate Degradation

    Directory of Open Access Journals (Sweden)

    Ahmet Ozan Gezerman


    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.

  8. Shock Initiation and Equation of State of Ammonium Nitrate (United States)

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


    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.

  9. Removal of vanadium from ammonium molybdate solution by ion exchange

    Institute of Scientific and Technical Information of China (English)

    LI Qing-gang; ZHANG Qi-xiu; ZENG Li; XIAO Lian-sheng; YANG Ya-nan


    The separation techniques of vanadium and molybdenum were summarized, and a new method of removal V(Ⅴ) from Mo(Ⅵ) by adsorption with chelate resin was presented. Nine kinds of chelate resins were used to investigate the adsorbent capability of V(Ⅴ) in ammonium molybdate solution with static method. The test results show that DDAS, CUW and CW-2 resins can easily adsorb V(Ⅴ) in ammonium molybdate solution, but hardly adsorb Mo(Ⅵ). The dynamic experimental results show more than 99.5% of V(Ⅴ) can be adsorbed, and the adsorption rate of Mo(Ⅵ) is less than 0.27% at 294-296 K for 60 min at pH 7.42-8.02. The mass ratio of V to Mo decreases to l/5 0000 in the effluent from 1/255 in the initial solution. The loaded resin can be desorbed by 5% NH3·H2O solution, and the vanadium desorption rate can reach 99.6%. The max concentration of vanadium in desorbed solution can reach 20 g/L, while the concentration of molybdenum is less than 0.8 g/L.

  10. Regulation by ammonium of glutamate dehydrogenase (NADP+) from Saccharomyces cerevisiae. (United States)

    Bogonez, E; Satrústegui, J; Machado, A


    The activity of glutamate dehydrogenase (NADP+) (EC; NADP-GDH) of Saccharomyces cerevisiae is decreased under conditions in which intracellular ammonia concentrations increases. A high internal ammonia concentration can be obtained (a) by increasing the ammonium sulphate concentration in the culture medium, and (b) by growing the yeast either in acetate + ammonia media, where the pH of the medium rises during growth, or in heavily buffered glucose + ammonia media at pH 7.5. Under these conditions cellular oxoglutarate concentrations do not vary and changes in NADP-GDH activity appear to provide a constant rate of oxoglutarate utilization. The following results suggest that the decrease in NADP-GDH activity in ammonia-accumulating yeast cells is brought about by repression of synthesis: (i) after a shift to high ammonium sulphate concentrations, the number of units of activity per cell decreased as the inverse of cell doubling; and (ii) the rate of degradation of labelled NADP-GDH was essentially the same in ammonia-accumulating yeast cells and in controls, whereas the synthesis constant was much lower in the ammonia-accumulating cells than in the controls.

  11. Fabrication and cytocompatibility of spherical magnesium ammonium phosphate granules. (United States)

    Christel, Theresa; Geffers, Martha; Klammert, Uwe; Nies, Berthold; Höß, Andreas; Groll, Jürgen; Kübler, Alexander C; Gbureck, Uwe


    Magnesium phosphate compounds, as for example struvite (MgNH4PO4·6H2O), have comparable characteristics to calcium phosphate bone substitutes, but degrade faster under physiological conditions. In the present work, we used a struvite forming calcium doped magnesium phosphate cement with the formulation Ca0.75Mg2.25(PO4)2 and an ammonium phosphate containing aqueous solution to produce round-shaped granules. For the fabrication of spherical granules, the cement paste was dispersed in a lipophilic liquid and stabilized by surfactants. The granules were characterized with respect to morphology, size distribution, phase composition, compressive strength, biocompatibility and solubility. In general, it was seen that small granules can hardly be produced by means of emulsification, when the raw material is a hydraulic paste, because long setting times promote coalescence of initially small unhardened cement droplets. Here, this problem was solved by using an aqueous solution containing both the secondary (NH4)2HPO4 and primary ammonium phosphates NH4H2PO4 to accelerate the setting reaction. This resulted in granules with 97 wt.% having a size in the range between 200 and 1,000 μm. The novel solution composition doubled the compressive strength of the cement to 37 ± 5 MPa without affecting either the conversion to struvite or the cytocompatibility using human fetal osteoblasts.

  12. Development of electrochemical denitrification from waste water containing ammonium nitrate

    Energy Technology Data Exchange (ETDEWEB)

    Sawa, Toshio; Hirose, Yasuo; Ishii, Yoshinori; Takatsudo, Atsushi; Wakasugi, Kazuhico; Hayashi, Hiroshi


    The authors developed processes to dentrify waste water containing ammonium nitrate discharged from the nuclear fuel manufacturing works and to recover nitric acid and ammonia. For denitrification they applied the operating method and the conditions of operation to make 0.4mM or less from NH{sub 4}NO{sub 3} waste water of 1.5 M by 3 stages of electrodialysis cells. To recover nitric acid and ammonium water, they separated HNO{sub 3} solution of 6 M and NH{sub 4}OH solution with one unit of electrolysis cell, then absorbed NH{sub 3} gas from NH{sub 4}OH solution with water and applied the condition of operation to recover 8 M NH{sub 4}OH solution. The authors demonstrated that treatment and recovery can be carried out stably with actual waste water with a system through the combination of previously mentioned electrodialysis cells, electrolysis cells and an ammonia gas absorber. At present they are planning a plant where NH{sub 4}NO{sub 3} waste water of 4,500 mol can be treated per day.

  13. 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


    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.

  14. Highly efficient hydrogen storage system based on ammonium bicarbonate/formate redox equilibrium over palladium nanocatalysts. (United States)

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


    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.

  15. Diastereoisomeric β-ethyl aspartate-cobalt(III) complexes: Λ(+)578- and Δ(-)578-bis(ethane-1,2-diamine)[β-ethyl (S)-aspartato]cobalt(III) bis(perchlorate) monohydrate. (United States)

    Hammershøi, Anders; Schau-Magnussen, Magnus; Bendix, Jesper; Mølgaard, Anne


    The structures of the diastereoisomers Λ(+)(578)-, (I), and Δ(-)(578)-bis(ethane-1,2-diamine)[β-ethyl (S)-aspartato-κ(2)N,O(1)]cobalt(III) bis(perchlorate) monohydrate, (II), both [Co(C(6)H(10)N(2)O(4))(C(2)H(8)N(2))(2)](ClO(4))(2)·H(2)O, are compared. In both structures, the ester group of the amino acid side chain is engaged only in intramolecular hydrogen bonding to coordinated amine groups. This interaction is stronger in (I) and correlates with previously observed diastereoisomeric equilibrium ratios for related metal complex systems in aqueous media. The two perchlorate anions of (II) are located on twofold axes. Both perchlorates in (I) and one of the perchlorates in (II) are affected by disorder. Both structures exhibit extensive three-dimensional hydrogen-bonding networks.

  16. Quantitative determination of perchlorate in bottled water and tea with online solid phase extraction high-performance liquid chromatography coupled to tandem mass spectrometry. (United States)

    Lin, Shu-Ling; Lo, Chih-Yu; Fuh, Ming-Ren


    Due to the similarity in ionic radius, perchlorate has been reported to inhibit the iodide intake in the thyroid gland, which may lead to low heart rate, weight gain, and fatigue. In recent years, the presence of perchlorate in drinking water, surface water, soil, and food supplies in the United States has raised a great concern on establishing the maximum residue limit (MRL) for perchlorate to reduce its possible adverse influence on human health. US EPA currently puts perchlorate on the final third Contamination Candidate List (CCL3) and suggests a health reference level at 4.9 μg L⁻¹. The MRL of perchlorate was therefore set at 5.0 μg L⁻¹ by the authors for method validation. In this study, large volume injection (up to 1-mL) and online solid phase extraction (SPE) were utilized for pre-concentrating perchlorate ions and removing unretained matrix components prior to reversed-phase HPLC analysis using ESI-tandem MS under the negative mode. After eluting perchlorate from online SPE, 0.1% formic acid solution was utilized for isocratic HPLC analysis without any organic solvent. Multiple reaction monitoring (MRM) and the internal standard, Cl₁₈O₄⁻, were utilized for quantitatively determining perchlorate in bottled water and bottled tea samples. Two linear ranges, 0.05-0.50 μg L⁻¹ and 0.50-10.00 μg L⁻¹, were established to better estimate the residual amounts of perchlorate in bottled water samples with a method detection limit (MDL, signal-to-noise ratio of 3) of 0.01 μg L⁻¹. The linear range was 1.50-10.00 μg L⁻¹ for bottled tea samples with a MDL of 0.5 μg L⁻¹. In addition, the proposed method was further validated based on the EU Commission Decision 2002/657/EC, including within-laboratory reproducibility, decision limit (CCα), and detection capability (CCβ) for bottled water and bottled tea samples. The intra-day/inter-day precision and accuracy as well as within-laboratory reproducibility were determined by calculating

  17. Phase behaviour and molecular dynamics in the binary system of sodium perchlorate and 1,2-propanediamine

    Energy Technology Data Exchange (ETDEWEB)

    Terashima, Yukio [Department of Natural Science Education, Joint Graduate School, Hyogo University of Teacher Education (Japan); Takeda, Kiyoshi, E-mail: [Department of Chemistry, Naruto University of Education, 748 Nakajima, Takashima Naruto-cho, Naruto, Tokushima 772-8502 (Japan); Honda, Makoto [Department of Physics, Naruto University of Education (Japan)


    The phase and glass transition behaviour in a binary mixture of sodium perchlorate and 1,2-propanediamine {l_brace}(NaClO{sub 4}){sub x}(12PDA){sub 1-x}, x < 0.40{r_brace} was investigated by differential scanning calorimetry and Raman scattering measurements. A eutectic point and a peritectic point were found at x = 0.17 and 0.19, respectively. The phase diagram indicates the existence of solvated compounds of (NaClO{sub 4}){sub 1}(12PDA){sub 4} and (NaClO{sub 4}){sub 2}(12PDA){sub 5}. The concentration dependence of the glass transition point shows a sigmoid curve implying an underlying anomaly.

  18. Concentration of zinc ions in perchlorate medium by a menbrane-gel using an acid extractant (DEHPA

    Directory of Open Access Journals (Sweden)

    Belhadji L.


    Full Text Available Recent decades, it is an awareness of the importance of ecological balance in the environment, balances threatened by industrial pollution. A new spirit presides we seek to minimize pollution of receiving waters. The present work is to study the liquid-gel-extraction of zinc ions in perchlorate medium by an acid extractant: the di (ethyl-2 hexyl phosphorique acid, or DEHPA. Two types of polymers were used as supports of solvent extraction: a polybutadiene rubber cross-linked respectively with 0.1% dicumyl peroxide and 0.4% dicumyl peroxide, vulcanized at 160°C, one is most cross-linked than the other. The liquid-gel extraction is based on the principles of the liquid-liquid extraction.

  19. Bis[(2-methylbenzylbis(pyridin-2-ylmethyl-κNamine-κN]manganese(II bis(perchlorate

    Directory of Open Access Journals (Sweden)

    Ray J. Butcher


    Full Text Available In the title complex, [Mn(C20H21N32](ClO42, two tridentate (2-methylbenzylbis(pyridin-2-ylmethylamine (L ligands form the MnII complex [MnL2](ClO42. The MnII ion lies on a twofold axis and the complex cation is significantly distorted from regular octahedral geometry. The packing is stabilized by weak C—H...O interactions between the cations and anions, which link them into a zigzag ribbon along [101]. The perchlorate anion is disordered and was constrained to be tetrahedral with two orientations having occupancies of 0.768 (4 and 0.232 (4. The 2-methylbenzyl moiety is also disordered over two sets of sites, with occupancies of 0.508 (15 and 0.492 (15.

  20. Kinetic studies on the formation of nitrosamines I. Formation of dimethylnitrosamine in aqeous solution of perchloric acid. (United States)

    Cachaza, J M; Casado, J; Castro, A; López Quintela, M A


    The kinetics of nitrosation of dimethylamine (DMA) in aqueous perchloric acid solution have been studied using a differential spectrophotometric technique. The rate law is Initial rate = e[DMA]0 [nitrite]2 0 [H+]/(f + [H+])2 where [DMA]0 and [nitrite]0 represent initial stoichiometric concentrations. At 310.0 K and mu = 2.0 M, e = (2.2 +/- 0.2) X 10(-5) M-1 s-1 and f = (1.28 +/- 0.02) X 10(-3) M. The associated activation energy is 56 +/- 3 kJ mol-1. A clear inhibition of the nitrosation rate by ionic strength has been observed in which only the kinetic parameter (f) has an effective change. It is concluded that under the experimental conditions of this work only the dinitrogen trioxid is the effective carrier for the nitrosation.

  1. Optimized geometry, vibration (IR and Raman spectra and nonlinear optical activity of p-nitroanilinium perchlorate molecule: A theoretical study

    Directory of Open Access Journals (Sweden)

    Tamer Ömer


    Full Text Available The molecular modeling of p-nitroanilinium perchlorate molecule was carried out by using B3LYP and HSEH1PBE levels of density functional theory (DFT. The IR and Raman spectra were simulated and the assignments of vibrational modes were performed on the basis of relative contribution of various internal co-ordinates. NBO analysis was performed to demonstrate charge transfer, conjugative interactions and the formation of intramolecular hydrogen bonding interactions within PNAPC. Obtained large dipole moment values showed that PNAPC is a highly polarizable complex, and the charge transfer occurs within PNAPC. Hydrogen bonding and charge transfer interactions were also displayed by small HOMO-LUMO gap and molecular electrostatic potential (MEP surface. The strong evidences that the material can be used as an efficient nonlinear optical (NLO material of PNAPC were demonstrated by considerable polarizability and hyperpolarizability values obtained at DFT levels.

  2. Structure effect of molybdenum (5) complexes on its activity in appearance of catalytic polarographic currents of chlorate- and perchlorate ions

    Energy Technology Data Exchange (ETDEWEB)

    Zajtsev, P.M.; Zhdanov, S.I.; Dergacheva, E.N.; Savchenko, E.N.; Nikolaeva, T.D. (Vsesoyuznyj Nauchno-Issledovatel' skij Inst. Khimicheskikh Reaktivov i Osobo Chistykh Veshchestv, Moscow (USSR))


    Polarographic behaviour and reactivity of synthesized molybdenum (5) in reactions, conditioning catalytic currents of ClO/sub 3//sup -/ and ClO/sub 4//sup -/ have been studied. Their comparison with similar characteristics for molybdenum (5) appearing in the process of Mo (6) solution polarography is made. For the purpose a salt of molybdenum (5) in H/sub 2/SO/sub 4/, HCl and HClO/sub 4/ solutions have been synthesized by electrochemical and chemical ways. It has been established that in reactions conditioning catalytic currents of chlorate- and perchlorate-ions the preservation of structure of Mo (6) complex in the Mo (5) complex formed, i.e. processes of Mo (5) complex ageing, plays a very significant role.

  3. Bis(acetonitrile-κN(1,10-phenanthroline-κ2N,N′platinum(II bis(perchlorate

    Directory of Open Access Journals (Sweden)

    Kwang Ha


    Full Text Available The asymmetric unit of the title compound, [Pt(CH3CN2(C12H8N2](ClO42, contains one half of a cationic PtII complex and pair of half perchlorate anions, one of which is disordered over two sites in a 0.53 (3:0.47 (3 ratio. The complex and anions are disposed about a crystallographic mirror plane parallel to the ac plane passing through the Pt and Cl atoms. In the complex, the PtII ion lies in a distorted square-planar environment defined by four N atoms of the chelating 1,10-phenanthroline ligand and two distinct acetonitrile molecules. The component ions interact by means of intermolecular C—H...O hydrogen bonds.

  4. Distribution of Natural Perchlorate in a Desert Landscape-Amargosa Desert Research Site, Nevada (United States)

    Andraski, B. J.; Jackson, A.; Welborn, T.; Stonestrom, D. A.; Bohlke, J. K.


    Knowledge of perchlorate (ClO4-) occurrence is important due to health concerns, evolving groundwater-protection regulations, and for forensic investigations. The distribution of natural ClO4- is being studied at the U.S. Geological Survey's Amargosa Desert Research Site to improve understanding of factors that influence its accumulation and cycling in a desert landscape. The first part of the study evaluated the effect of plants on shallow (0-30 cm) soil concentrations in three settings-shoulder slope, footslope, and valley floor; samples were collected adjacent to plants and in interspaces 2.5-5 m from plants. For the valley-floor, there was a 17-fold decrease between interspace (5.0 μg/kg) and plant-adjacent (0.3 μg/kg) ClO4- concentrations. Chloride (Cl-) concentrations also showed large differences and indicated salt accumulation beneath the interspace desert pavement, but localized leaching adjacent to plants. For the shoulder and footslope, differences between interspace and plant-adjacent ClO4- concentrations were smaller (two fold on average) and inverted (interspace 2.0 μg/kg; plant-adjacent 3.8 μg/kg), and differences between interspace and plant-adjacent Cl- were negligible. Shoulder and footslope indications of a localized increase in ClO4- adjacent to plants suggest a cyclic mechanism of plant uptake, bioaccumulation, and leaf drop. The second part of the study examined ClO4- variability across a 9-ha hillslope. Data first were analyzed by assigning each sampling point to one of three elevation bands-upper, middle, or lower. Soil and plant data both showed trends of increasing ClO4- with decreasing elevation. Concentrations were, for soil (μg/kg): upper (1.6) middle (3.9) > lower (3.6). Multiple-linear regression analyses also were used to explore the relative importance of soil, plant, and terrain variables that influenced ClO4- concentrations across the hillslope. Important explanatory variables for soil ClO4- are land-surface elevation and

  5. Evidence for Perchlorates and the Origin of Chlorinated Hydrocarbons Detected by SAM at the Rocknest Aeolian Deposit in Gale Crater (United States)

    Glavin, Daniel P.; Freissinet, Caroline; Miller, Kristen E.; Eigenbrode, Jennifer L.; Brunner, Anna E.; Buch, Arnaud; Sutter, Brad; Archer, P. Douglas, Jr.; Atreya, Sushil K.; Brinckerhoff, William B.; Cabane, Michel; Coll, Patrice; Conrad, Pamela G.; Coscia, David; Dworkin, Jason P.; Franz, Heather B.; Grotzinger, John P.; Leshin, Laurie A.; Martin, Mildred G.; McKay, Christopher; Ming, Douglas W.; Navarro-Gonzalez, Rafael; Pavlov, Alexander; Steele, Andrew; Summons, Roger E.; Szopa, Cyril; Teinturier, Samuel; Mahaffy, Paul R.


    A single scoop of the Rocknest aeolian deposit was sieved (less than 150 micrometers), and four separate sample portions, each with a mass of approximately 50 mg, were delivered to individual cups inside the Sample Analysis at Mars (SAM) instrument by the Mars Science Laboratory rover's sample acquisition system. The samples were analyzed separately by the SAM pyrolysis evolved gas and gas chromatograph mass spectrometer analysis modes. Several chlorinated hydrocarbons including chloromethane, dichloromethane, trichloromethane, a chloromethylpropene, and chlorobenzene were identified by SAM above background levels with abundances of approximately 0.01 to 2.3 nmol. The evolution of the chloromethanes observed during pyrolysis is coincident with the increase in O2 released from the Rocknest sample and the decomposition of a product of N-methyl-N-(tert-butyldimethylsilyl)-trifluoroacetamide (MTBSTFA), a chemical whose vapors were released from a derivatization cup inside SAM. The best candidate for the oxychlorine compounds in Rocknest is a hydrated calcium perchlorate (Ca(ClO4)2·nH2O), based on the temperature release of O2 that correlates with the release of the chlorinated hydrocarbons measured by SAM, although other chlorine-bearing phases are being considered. Laboratory analog experiments suggest that the reaction of Martian chlorine from perchlorate decomposition with terrestrial organic carbon from MTBSTFA during pyrolysis can explain the presence of three chloromethanes and a chloromethylpropene detected by SAM. Chlorobenzene may be attributed to reactions of Martian chlorine released during pyrolysis with terrestrial benzene or toluene derived from 2,6-diphenylphenylene oxide (Tenax) on the SAM hydrocarbon trap. At this time we do not have definitive evidence to support a nonterrestrial carbon source for these chlorinated hydrocarbons, nor do we exclude the possibility that future SAM analyses will reveal the presence of organic compounds native to the

  6. The perchlorate discharge test with {sup 123}I for the diagnosis of the Pendred syndrome in children; Der Depletionstest mit {sup 123}Iod zur Diagnose des Pendred-Syndroms bei Kindern

    Energy Technology Data Exchange (ETDEWEB)

    Hahn, K.; Fischer, S. [Klinik und Poliklinik fuer Nuklearmedizin, Klinikum der Ludwig-Maximilians-Univ. Muenchen (Germany)


    The method for the diagnosis of the Pendred Syndrome in children by the Perchlorate discharge test using {sup 123}I is described. The older child, who has the Pendred Syndrome and the obligatory hearing deficit, frequently has neither a goitre nor hypothyroidism, but other investigations (bone growth, scars and function tests) can also show changes. However a more certain diagnosis of this disorder in children is possible by the perchlorate discharge test using {sup 123}I. (orig.)

  7. Formation and transformation of metastable double salts from the crystallization of mixed ammonium nitrate and ammonium sulfate particles. (United States)

    Ling, Tsz Yan; Chan, Chak K


    Ammonium nitrate (AN) and ammonium sulfate (AS) are ubiquitous components of atmospheric aerosols. Thermodynamic models predict formation of pure (AN and AS) and double salts (3AN. AS and 2AN. AS) for the AN/AS system. Because of the high supersaturation at which a droplet crystallizes, metastable crystal formation is possible. In this study, the identity of the crystals formed from the crystallization of equimolar AN/AS mixed droplets was investigated in an electrodynamic balance coupled with a Raman spectroscopic system. Raman spectra of bulk AN/AS double salts possibly formed in this system are first reported for comparison with the single particle Raman results. The double-salt 3AN. AS, not predicted from thermodynamics, was observed in the freshly crystallized single particles. The degree of metastability can be different among several crystallization processes of the same particles. The metastable salt 3AN. AS gradually transformed into stable 2AN. AS, and the rate of such transformation increased with increasing relative humidity. This study illustrates the possibility of occurrence of metastable salts in atmospheric aerosols.

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

  9. 生物修复高氯酸盐污染的研究进展%Research advance in bioremediation technology of perchlorate contamination

    Institute of Scientific and Technical Information of China (English)

    高海硕; 陈桂葵; 黎华寿


    生物修复技术是目前高氯酸盐污染环境整治的最具潜力的修复技术之一,具有成本低、无二次污染的特点,是国内外一个新的研究热点,亦是仅见的污染控制及修复的环境友好技术.介绍了环境中高氯酸盐污染的来源与分布,阐述了生物修复(主要包括植物修复和微生物修复)的特点及作用机制,认识到2种类型修复技术各有其优劣势;重点综述了生物修复高氯酸盐污染的国内外研究现状,得出植物根际降解对植物修复高氯酸盐起着十分重要作用,而微生物修复是目前最有希望获得大规模应用的高氯酸盐污染修复技术;最后提出了植物微生物联合强化修复高氯酸盐污染的技术将更具应用前景.%Bioremediation is the most potential technologies in perchlorate contamination remediation. As the only environmentally friendly remediation technologies so far, bioremediation technology had the advantage of low cost and no secondary pollution,it become a new research hotspot at home and abroad. This paper introduced the source and distribution of perchlorate contamination,described the characteristics and mechanism of bioremediation technology (mainly included phytoremediation and microbial remediation) in perchlorate contamination remediation; the advantages and disadvantages of these two bioremediation techniques was summarized and compared. The research status of perchlorate contamination bioremediation was reviewed. It was found that plant rhizosphere degradation played an important role in phytoremediation;microbial remediation was the most hopeful technology for large-scale application in perchlorate pollution remediation. The phyto-microbial strengthen remediation technology was put forward; it would had more application prospects in perchlorate contamination remeditation.

  10. Quantitative remote sensing of ammonium minerals, Cedar Mountains, Esmeralda County, Nevada (United States)

    Baugh, William M.; Kruse, Fred A.


    Mineral-bound ammonium (NH4+) was discovered by the U.S. Geological Survey in the southern Cedar Mountains of Esmeralda County, Nevada in 1989. At 10 km in length, this site is 100 times larger than any previously known occurrence in volcanic rocks. The ammonium occurs in two hydrothermally altered, crystal-rich rhyolitic tuff units of Oligocene age, and is both structurally and stratigraphically controlled. This research uses Advanced Visible/Infrared Imaging Spectrometer (AVIRIS) data to quantitatively map the mineral-bound ammonium (buddingtonite) concentration in the altered volcanic rocks. Naturally occurring mineral-bound ammonium is fairly rare; however, it has been found to occur in gold-bearing hydrothermal deposits. Because of this association, it is thought that ammonium may be a useful too in exploration for gold and other metal deposits. Mineral-bound ammonium is produced when an ammonium ion (NH4+) replaces the alkali cation site (usually K+) in the crystal structure of silicate minerals such as feldspars, micas and clays. Buddingtonite is an ammonium feldspar. The ammonium originates in buried organic plant matter and is transported to the host rock by hydrothermal fluids. Ammonium alteration does not produce visible changes in the rock, and it is barely detectable with standard x-ray diffraction methods. It is clearly identified, however, by absorption features in short wave-infrared (SWIR) wavelengths (2.0 - 2.5 micrometers). The ammonium absorption features are believed to be caused by N-H vibrational modes and are analogous to hydroxyl (O-H) vibrational modes, only shifted slightly in wavelength. Buddingtonite absorption features in the near- and SWIR lie at 1.56, 2.02 and 2.12 micrometers. The feature at 2.12 micrometer is the strongest of the three and is the only one used in this study. The southern Cedar Mountains are sparsely vegetated and are an ideal site for a remote sensing study.

  11. Contributions of two cytosolic glutamine synthetase isozymes to ammonium assimilation in Arabidopsis roots. (United States)

    Konishi, Noriyuki; Ishiyama, Keiki; Beier, Marcel Pascal; Inoue, Eri; Kanno, Keiichi; Yamaya, Tomoyuki; Takahashi, Hideki; Kojima, Soichi


    Glutamine synthetase (GS) catalyzes a reaction that incorporates ammonium into glutamate and yields glutamine in the cytosol and chloroplasts. Although the enzymatic characteristics of the GS1 isozymes are well known, their physiological functions in ammonium assimilation and regulation in roots remain unclear. In this study we show evidence that two cytosolic GS1 isozymes (GLN1;2 and GLN1;3) contribute to ammonium assimilation in Arabidopsis roots. Arabidopsis T-DNA insertion lines for GLN1;2 and GLN1;3 (i.e. gln1;2 and gln1;3 single-mutants), the gln1;2:gln1;3 double-mutant, and the wild-type accession (Col-0) were grown in hydroponic culture with variable concentrations of ammonium to compare their growth, and their content of nitrogen, carbon, ammonium, and amino acids. GLN1;2 and GLN1;3 promoter-dependent green fluorescent protein was observed under conditions with or without ammonium supply. Loss of GLN1;2 caused significant suppression of plant growth and glutamine biosynthesis under ammonium-replete conditions. In contrast, loss of GLN1;3 caused slight defects in growth and Gln biosynthesis that were only visible based on a comparison of the gln1;2 single- and gln1;2:gln1;3 double-mutants. GLN1;2, being the most abundantly expressed GS1 isozyme, markedly increased following ammonium supply and its promoter activity was localized at the cortex and epidermis, while GLN1;3 showed only low expression at the pericycle, suggesting their different physiological contributions to ammonium assimilation in roots. The GLN1;2 promoter-deletion analysis identified regulatory sequences required for controlling ammonium-responsive gene expression of GLN1;2 in Arabidopsis roots. These results shed light on GLN1 isozyme-specific regulatory mechanisms in Arabidopsis that allow adaptation to an ammonium-replete environment.

  12. Assessment of the potential for ammonium nitrate formation and reaction in Tank 241-SY-101

    Energy Technology Data Exchange (ETDEWEB)

    Pederson, L.R.; Bryan, S.A.


    Two principal scenarios by which ammonium nitrate may be formed were considered: (a) precipitation of ammonium nitrate in the waste, and (b) ammonium nitrate formation via the gas phase reaction of ammonia and nitrogen dioxide. The first of these can be dismissed because ammonium ions, which are necessary for ammonium nitrate precipitation, can exist only in negligibly small concentrations in strongly alkaline solutions. Gas phase reactions between ammonia, nitrogen dioxide, and water vapor in the gas phase represent the most likely means by which ammonium nitrate aerosols could be formed in Tank 241-SY-101. Predicted ammonium nitrate formation rates are largely controlled by the concentration of nitrogen dioxide. This gas has not been detected among those gases vented from the wastes using Fourier Transform Infrared Spectrometry (FTIR) or mass spectrometry. While detection limits for nitrogen dioxide have not been established experimentally, the maximum concentration of nitrogen dioxide in the gas phase in Tank 241-SY-101 was estimated at 0.1 ppm based on calculations using the HITRAN data base and on FTIR spectra of gases vented from the wastes. At 50 C and with 100 ppm ammonia also present, less than one gram of ammonium nitrate per year is estimated to be formed in the tank. To date, ammonium nitrate has not been detected on HEPA filters in the ventilation system, so any quantity that has been formed in the tank must be quite small, in good agreement with rate calculations. The potential for runaway exothermic reactions involving ammonium nitrate in Tank 241-SY-101 is minimal. Dilution by non-reacting waste components, particularly water, would prevent hazardous exothermic reactions from occurring within the waste slurry, even if ammonium nitrate were present. 41 refs.

  13. 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


    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.

  14. Rotavirus gastroenteritis-associated urinary ammonium acid urate crystals. (United States)

    Yokoyama, Tadafumi; Sugimoto, Naotoshi; Kato, Eiji; Ohta, Kazuhide; Ishikawa, Sayaka; Ueno, Kazuyuki; Shimizu, Masaki; Yachie, Akihiro


    Although ammonium acid urate (AAU) calculi are extremely rare renal stone components, it was recently found that many urinary tract calculi that cause post-renal renal failure in rotavirus (RV) gastroenteritis are AAU calculi. The mechanism of AAU calculi development in RV gastroenteritis has not been fully elucidated. We analyzed data from eight RV gastroenteritis patients who transiently had AAU crystals in their urinary sediment. In these patients, formation of AAU crystals occurred earlier than the formation of AAU calculi. No difference was observed in serum and urine uric acid levels between RV gastroenteritis patients with or without AAU crystals. Interestingly, fractional excretion of sodium was extremely low among patients with AAU crystals. These results suggest that the formation of AAU crystals might not be due to excretion of uric acid, but excretion of sodium.

  15. 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)


    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.

  16. Synthesis of tetramethyl ammonium hydroxide by cell diaphragm electrolytic method

    Institute of Scientific and Technical Information of China (English)


    Under the conditions of tetramethyl ammonia chloride (TMAC) used as starting material, Ti-based Dimensionally Stable Anode (DSA), stainless steel used as cathode and Nafion 900 cation membrane as cell diaphragm, this paper studies the synthesis of tetramethyl ammonium hydroxide (TMAH) by cell diaphragm electrolytic method, examining not only the effects of current density, concentration of starting material and cell temperature, on the product purity and current efficiency, but also the effects of electrolyte circulation rate on the service life of Ti-based DSA.The experiment puts forward an optimum processing condition, and experimental findings show that preparing TMAH by using this technique can obtain a current efficiency 74.7 % and get product with a purity greater than 99.9%.

  17. Computational Modeling of Degradation of Substituted Benzyltrimethyl Ammonium: Preprint

    Energy Technology Data Exchange (ETDEWEB)

    Long, H.; Pivovar, B. S.


    The degradation of cations on the alkaline exchange membranes is the major challenge for alkaline membrane fuel cells. In this paper, we investigated the degradation barriers by density functional theory for substituted benzyltrimethyl ammonium (BTMA+) cations, which is one of the most commonly used cations for alkaline exchange membranes. We found that substituted cations with electron-releasing substituent groups at meta-position of the benzyl ring could result in improved degradation barriers. However, after investigating more than thirty substituted BTMA+ cations with ten different substituent groups, the largest improvement of degradation barriers is only 1.6 kcal/mol. This implies that the lifetime of alkaline membrane fuel cells could increase from a few months to a few years by using substituted BTMA+ cations, an encouraging but still limited improvement for real-world applications.

  18. 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)


    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.

  19. 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


    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.

  20. 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: [Hebrew University of Jerusalem, Department of Medicinal Chemistry and Natural Products, School of Pharmacy, Faculty of Medicine (Israel)


    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.

  1. Ammonium nitrate emulsion : physical properties and decomposition using thermal methods

    Energy Technology Data Exchange (ETDEWEB)

    Feng, H.; Goldthorp, S.; Singh, S.; Turcotte, R.


    This presentation discussed methods of determining the physical properties and decomposition rates of commercial water-based explosives. Ammonium nitrate emulsions can explode when heated to critical temperatures or when a localized thermal energy deposition occurs. An accelerating rate calorimeter (ARC) was used to investigate the emulsion under adiabatic conditions. Simultaneous mass spectroscopy (MS) Fourier Transform Infrared (FTIR) and differential scanning calorimetry (DSC) techniques were used to conduct an evolved gas analysis. Results of the analysis demonstrated that the AN emulsions have ARC onset temperatures of approximately 220 degrees C. The mass loss reaction occurred in 2 steps. The initial step was related to water evaporation and oil phase volatilization. The second step was related to AN decomposition in a closed system, and AN dissociation in an open system. tabs., figs.

  2. Lactulose production from cheese whey using recyclable catalyst ammonium carbonate. (United States)

    Seo, Yeong Hwan; Sung, Mina; Han, Jong-In


    Ammonium carbonate ((NH4)2CO3) was used as an alkaline catalyst of lactulose production from cheese whey. Maximum yield of 29.6% was obtained at reaction time of 28.44 min, (NH4)2CO3 of 0.76% at 97°C. During reaction, (NH4)2CO3 was fully decomposed to NH3 and CO2, and these gases were recovered. To boost up NH3 recovery, various methods such as heating, aeration, and pH adjustment were applied. The optimal condition for the purpose of NH3 retrieval was temperature of up to 60°C alongside aeration. Easy separation and recovery make (NH4)2CO3 a catalyst alternative to common alkaline chemicals especially for the weak alkaline reaction.

  3. 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


    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.

  4. Polishing of quartz by rapid etching in ammonium bifluoride. (United States)

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


    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.

  5. Polymerization and photochromism of ammonium molybdate in porous glass (United States)

    Pak, V. N.; Borisov, A. N.


    Modification of porous glass (PG) plates is carried out by impregnation with aqueous solutions of ammonium molybdate (NH4)2MoO4 with subsequent removal of water at 120°C. A long-wavelength shift of absorption spectra upon accumulation of the salt in PG indicates polymerization of MoO 4 2- anions at low concentrations of the encapsulated salt. Photochromism manifests itself as the anionic forms in PG become larger. UV irradiation of the modified plates causes enhancement of continuous absorption in the visible range. The proposed mechanism of photoreduction of the polianions in PG involves the removal of oxygen atoms from the bridging-Mo-O-Mo-bonds and stabilization of the colored forms by means of conjugation of the electrons released from the 4 d-levels of pentavalent molybdenum.

  6. Crystal structure of tris-(hydroxyl-ammonium) orthophosphate. (United States)

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


    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.

  7. Antibacterial effect of composite resins containing quaternary ammonium polyethyleneimine nanoparticles (United States)

    Yudovin-Farber, Ira; Beyth, Nurit; Weiss, Ervin I.; Domb, Abraham J.


    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.

  8. Cold Case: Radar investigation of ammonium sulfate cryovolcanism on Titan (United States)

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


    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).

  9. 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.


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

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

    NARCIS (Netherlands)

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


    . 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

  11. Ammonium sorption from aqueous solutions by the natural zeolite Transcarpathian clinoptilolite studied under dynamic conditions. (United States)

    Sprynskyy, Myroslav; Lebedynets, Mariya; Terzyk, Artur P; Kowalczyk, Piotr; Namieśnik, Jacek; Buszewski, Bogusław


    The scope of this study is ammonium-ion uptake from synthetic aqueous solutions onto raw and pretreated forms of the natural zeolite Transcarpathian clinoptilolite under dynamic conditions. Hydrogen ions displaced exchangeable cations on the clinoptilolite in distilled water (sodium ions) and hydrochloric acid (sodium, potassium, and calcium ions) and destroyed the zeolite framework structure in the last case. Ammonium uptake onto the zeolite occurs by exchange with Na(+), Ca(2+), and K(+) ions. Although Na(+) ions were observed to be more easily exchanged for both hydrogen and ammonium ions, the role of Ca(2+) ions increased with zeolite saturation by NH(+)(4) ions. The maximum sorption capacity of the clinoptilolite toward NH(+)(4) ions, estimated under dynamic conditions, is significantly higher than that measured under static conditions; proximity of the values of a distribution coefficient and a retardation factor for different conditions (215-265 dm(3)/kg and 979-1107, respectively) allows us to use these parameters to model ammonium uptake onto the clinoptilolite. Slowing down or interruption in filtration resulted in the improvement of ammonium sorption properties of the zeolite. The ammonium removal improves with use of the finer fractions of the clinoptilolite up to 0.35 mm. A recycling study results confirmed the importance of external diffusion for ammonium sorption by the clinoptilolite. Preliminary treatment of the sorbent confirmed the predominant importance of the ion-exchange mechanism. The advantage of prior NaCl treatment of the clinoptilolite in improvement of ammonium removal over the other techniques was shown.

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

    DEFF Research Database (Denmark)

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


    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, whic...

  13. Electroantennogram and behavioral responses of Anastrepha suspensa (Diptera: Tephritidae) to putrescine and ammonium bicarbonate lures. (United States)

    Kendra, Paul E; Montgomery, Wayne S; Epsky, Nancy D; Heath, Robert R


    At present, the most effective synthetic lures for pest Anastrepha fruit flies are multicomponent blends that include ammonia and the diamine synergist putrescine (1,4-diaminobutane). Both chemicals generally have been regarded as protein cues that result in female-biased attraction. Using electroantennography (EAG) and flight tunnel bioassays, this study evaluated response of the Caribbean fruit fly, Anastrepha suspensa (Loew) to vapors released from commercial lure formulations of ammonium bicarbonate and putrescine. Over a range of doses tested, EAG response to ammonium bicarbonate was equivalent for both sexes, but female response was significantly greater than male response to putrescine and to a 1:1 mixture of ammonium bicarbonate and putrescine. Amplitude of EAG response to the mixture was approximately equal to the summation of responses to the individual substrates. Using a fixed dose of substrate, EAG measurements from females 1-14 d old indicated that antennal sensitivity to both lures varied according to physiological state of the fly. Peak response to ammonium bicarbonate was recorded from immature females, peak response to putrescine from sexually mature females. In bioassays, more females were captured with ammonium bicarbonate plus putrescine than with ammonium bicarbonate alone. This difference was not observed in males, resulting in a higher female to male ratio in captures with ammonium bicarbonate plus putreseine (3:1) versus ammonium bicarbonate alone (1:1). Results suggest that separate olfactory receptors are involved in detection of the two semiochemicals, and that the putrescine component is primarily responsible for the female-biased attraction.

  14. 40 CFR 721.10154 - Quaternary ammonium compounds, dicoco alkyldimethyl, chlorides, reaction products with silica. (United States)


    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Quaternary ammonium compounds, dicoco alkyldimethyl, chlorides, reaction products with silica. 721.10154 Section 721.10154 Protection of Environment... SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10154 Quaternary ammonium...

  15. 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


    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.

  16. Ammonium-oxidizing bacteria facilitate aerobic degradation of sulfanilic acid in activated sludge. (United States)

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


    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.

  17. On the influence of thiamine and ammonium ions on alcoholic fermentation

    NARCIS (Netherlands)

    Maesen, Th.J.M.


    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

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

    DEFF Research Database (Denmark)

    Novak, John Thomas


    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...

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

    Directory of Open Access Journals (Sweden)

    Shavkat Namazov


    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.

  20. Ammonium assimilation: An important accessory during aerobic denitrification of Pseudomonas stutzeri T13. (United States)

    Sun, Yilu; Feng, Liang; Li, Ang; Zhang, Xuening; Yang, Jixian; Ma, Fang


    The present study investigated effect of ammonium utilization on aerobic denitrification by Pseudomonas stutzeri T13. Per nitrogen balance calculation, all consumed ammonium was utilized as nitrogen source for cell propagation by assimilation rather than heterotrophic nitrification. Total organic carbon (TOC) and ammonium were necessary substrates to sustain heterotrophic propagation of P. stutzeri T13 at optimum proportion equal to seven. Under aerobic condition, nitrate was utilized as substitute nitrogen source when ammonium was completely exhausted. Biomass production effectively increased with increasing initial ammonium from 0mg/L to 100mg/L. Owing to enlarged biomass, average nitrate reduction rate increased from 7.36mgL(-1)h(-1) to 11.95mgL(-1)h(-1). Such process also successfully reduced nitrite accumulation from 121.8mg/L to 66.16mg/L during aerobic denitrification. As important accessory during aerobic denitrification, ammonium assimilation efficiently doubled total nitrogen (TN) removal from 54.97mg/L (no ammonium provided) to 113.1mg/L (100mg/L ammonium involved).

  1. 75 FR 56489 - Separation Distances of Ammonium Nitrate and Blasting Agents From Explosives or Blasting Agents... (United States)


    ... Ammonium Nitrate and Blasting Agents From Explosives or Blasting Agents (2002R-226P) AGENCY: Bureau of... CFR 555.220 set forth a table of separation distances of ammonium nitrate and blasting agents from explosives or blasting agents followed by six explanatory notes. Note three (3) states that the...

  2. Sulfuric acid-ammonium sulfate aerosol: optical detection in the St. Louis region. (United States)

    Charlson, R J; Vanderpol, A H; Covert, D S; Waggnoner, A P; Ahlquist, N C


    Nephelometric sensing of the deliquescence of ammonium sulfate produced by the reaction of sulfuric acid or ammonium bisulfate aerosol with ammonia provides a means for detecting these substances in air. Field experiments show them to be the dominant substances in the submicrometer, light-scattering aerosol in the St. Louis region.

  3. 75 FR 41725 - Food Additives Permitted in Feed and Drinking Water of Animals; Ammonium Formate (United States)


    ... Additives Permitted in Feed and Drinking Water of Animals; Ammonium Formate AGENCY: Food and Drug... regulations for food additives permitted in feed and drinking water of animals to provide for the safe use of ammonium formate as an acidifying agent in swine feed. This action is in response to a food...

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

    CERN Document Server

    Cohen-Adad, R


    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.

  5. Suppression of interference in the AAS determination of chromium by use of ammonium bifluoride. (United States)

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


    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.

  6. Irritant contact dermatitis due to ammonium bifluoride in two infant twins. (United States)

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


    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.

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

    Directory of Open Access Journals (Sweden)

    Pongsak (Lek Noophan


    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.

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

    NARCIS (Netherlands)

    Casadella, Anna; Schaetzle, Olivier; Loos, Katja


    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

  9. 高氯酸铵粒度对AP-CMDB推进剂热分解特性的影响%Effects of granularity of ammonium perchlorate on thermal decomposition of AP-CMDB propellant

    Institute of Scientific and Technical Information of China (English)

    李吉祯; 樊学忠; 刘小刚; 刘子如


    利用热分析一质谱和红外联用法、高压差示扫描量热法研究了高氯酸铵(AP)粒度对AP-CMDB推进剂在0.1 MPa(常压)和1.0MPa压强下的热分解过程.结果表明,含不同粒度AP的AP-CMDB推进剂的热分解过程存在明显的差异,含大粒度AP(d50=96.8 μm)的推进剂在常压和1.0 MPa下的热分解过程均出现了AP单体的高温分解阶段,含小粒度AP(d50=12.4,8.5和1.0 μm)的推进剂在高压下均仅表现出一个快速分解阶段;AP-CMDB推进剂分解过程中的气体产物主要包括NO2,NO,N2O,CO2,CO,O2,N2,H2O,HCHO和HCl.

  10. Oxidation of alginate and pectate biopolymers by cerium(IV) in perchloric and sulfuric acid solutions: A comparative kinetic and mechanistic study. (United States)

    Fawzy, Ahmed


    The kinetics of oxidation of alginate (Alg) and pectate (Pec) carbohydrate biopolymers was studied by spectrophotometry in aqueous perchloric and sulfuric acid solutions at fixed ionic strengths and temperature. In both acids, the reactions showed a first order dependence on [Ce(IV)], whereas the orders with respect to biopolymer concentrations are less than unity. In perchloric acid, the reactions exhibited less than unit orders with respect to [H(+)] whereas those proceeded in sulfuric acid showed negative fractional-first order dependences on [H(+)]. The effect of ionic strength and dielectric constant was studied. Probable mechanistic schemes for oxidation reactions were proposed. In both acids, the final oxidation products were characterized as mono-keto derivatives of both biopolymers. The activation parameters with respect to the slow step of the mechanisms were computed and discussed. The rate laws were derived and the reaction constants involved in the different steps of the mechanisms were calculated.

  11. Control of Sulfidogenesis Through Bio-oxidation of H2S Coupled to (per)chlorate Reduction

    Energy Technology Data Exchange (ETDEWEB)

    Gregoire, Patrick [Univ. of California, Berkeley, CA (United States); Engelbrektson, Anna [Univ. of California, Berkeley, CA (United States); Hubbard, Christopher G. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Metlagel, Zoltan [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Csencsits, Roseann [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Auer, Manfred [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Conrad, Mark E. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Thieme, Jurgen [Brookhaven National Lab. (BNL), Upton, NY (United States); Northrup, Paul [Brookhaven National Lab. (BNL), Upton, NY (United States); Coates, John D. [Univ. of California, Berkeley, CA (United States)


    Here, we investigate H2S attenuation by dissimilatory perchlorate-reducing bacteria (DPRB). All DPRB tested oxidized H2S coupled to (per)chlorate reduction without sustaining growth. H2S was preferentially utilized over organic electron donors resulting in an enriched (34S)-elemental sulfur product. Electron microscopy revealed elemental sulfur production in the cytoplasm and on the cell surface of the DPRB Azospira suillum. We also propose a novel hybrid enzymatic-abiotic mechanism for H2S oxidation similar to that recently proposed for nitrate-dependent Fe(II) oxidation. The results of this study have implications for the control of biosouring and biocorrosion in a range of industrial environments.

  12. Interactions between nitrate and ammonium in their uptake, allocation, assimilation, and signaling in plants. (United States)

    Hachiya, Takushi; Sakakibara, Hitoshi


    Nitrogen (N) availability is a major factor determining plant growth and productivity. Plants acquire inorganic N from the soil, mainly in the form of nitrate and ammonium. To date, researchers have focused on these N sources, and demonstrated that plants exhibit elaborate responses at both physiological and morphological levels. Mixtures of nitrate and ammonium are beneficial in terms of plant growth, as compared to nitrate or ammonium alone, and therefore synergistic responses to both N sources are predicted at different steps ranging from acquisition to assimilation. In this review, we summarize interactions between nitrate and ammonium with respect to uptake, allocation, assimilation, and signaling. Given that cultivated land often contains both nitrate and ammonium, a better understanding of the synergism between these N sources should help to identify targets with the potential to improve crop productivity.

  13. 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


    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.

  14. The Investigation of Magnesium Perchlorate/Iron Phase-mineral Mixtures as a Possible Source of Oxygen and Chlorine Detected by the Sample Analysis at Mars (SAM) Instrument in Gale Crater, Mars (United States)

    Sutter, B.; Heil, E.; Archer, P. D.; Ming, D. W.; Eigenbrode, J. L.; Franz, H. B.; Glavin, D. P.; McAdam, A. C.; Mahaffy, P. R.; Niles, P. B.; Stern, J. C.; Navarro-Gonzalez, R.; McKay, C. P.


    The Sample Analysis at Mars (SAM) instrument onboard the Curiosity rover detect-ed O2 and HCl gas releases from the Rocknest (RN) eolian bedform and the John Klein (JK) and Cumber-land (CB) drill hole materials in Gale Crater (Fig. 1) [1,2]. Chlorinated hydrocarbons have also been detect-ed by the SAM quadrupole mass spectrometer (QMS) and gas chromatography/mass spectrometer (GCMS) [1,2,3,4]. These detections along with the detection of perchlorate (ClO4(-)) by the Mars Phoenix Lander's Wet Chemistry Laboratory (WCL) [5] suggesting perchlo-rate is a possible candidate for evolved O2 and chlorine species. Laboratory thermal analysis of individual per-chlorates has yet to provide an unequivocal tempera-ture match to the SAM O2 and HCl release data [1,2]. Catalytic reactions of Fe phases in the Gale Crater ma-terial with perchlorates can potentially reduce the de-composition temperatures of these otherwise pure per-chlorate/chlorate phases [e.g., 6,7]. Iron mineralogy found in the Rocknest materials when mixed with Ca-perchlorate was found to cause O2 release temperatures to be closer match to the SAM O2 release data and enhance HCl gas releases. Exact matches to the SAM data has unfortnunately not been achieved with Ca-perchlorate-Fe-phase mixtures [8]. The effects of Fe-phases on magnesium perchlorate thermal decomposi-tion release of O2 and HCl have not been evaluated and may provide improved matches to the SAM O2 and HCl release data. This work will evaluate the thermal decomposition of magnesium perchlorate mixed with fayalite/magnetite phase and a Mauna Kea palagonite (HWMK 919). The objectives are to 1) summarize O2 and HCl releases from the Gale Crater materials, and 2) evaluate the O2 and HCl releases from the Mg-perchlorate + Fe phase mixtures to determine if Mg-perchlorate mixed with Fe-phases can explain the Gale Crater O2 and HCl releases.

  15. Field Demonstration and Validation of a New Device for Measuring Groundwater and Perchlorate Fluxes at IHDIV-NSWC, Indian Head, MD (United States)


    potential hazard associated with this activity is exposure to perchlorate present in the ground water through skin contact. Waterproof , chemical... Waterproof , chemical resistant gloves shall be worn by site personnel when sub-sampling the PFMs and transferring to sample vials. 1.4.4 Site...water or disinfectant moist towelettes before eating, drinking, smoking, or applying cosmetics . These activities will be restricted to the designated

  16. Comparative Demonstration of Active and Semi-Passive In Situ Bioremediation Approaches for Perchlorate Impacted Groundwater: Active In Situ Bioremediation Demonstration (Aerojet Facility) (United States)


    zone; and (3) potential negative impacts of the electron donor addition on secondary water characteristics. 8.4 Pr ocur ement I ssues There are no...chlorine dioxide generator CDHS California Department of Health Services CDWR California Department of Water Resources cis-1,2-DCE cis-1,2...industry in the manufacturing, testing, and firing of rockets and missiles. Perchlorate exhibits high solubility and mobility in water and has been

  17. Preparation and Application of Perchloric Acid Supported on Alumina (Al2O3-HCIO4) to the Synthesis of α-(α-Amidobenzyl)-β-naphthols

    Institute of Scientific and Technical Information of China (English)



    Preparation of perchloric acid supported on alumina and its primary application as a solid supported heterogeneous catalyst to the synthesis of α-(α-amidobenzyl)-β-naphthols by a one-pot,three-component condensation of benzaldehydes,β-naphthol and acetamide or benzamide under thermal solvent-free conditions were described.The present methodology offers several advantages such as simple procedure,shorter reaction time,and excellent yields.

  18. Contrasting coordination behavior of Group 12 perchlorate salts with an acyclic N3O2 donor ligand by X-ray crystallography and (1)H NMR. (United States)

    Tice, Daniel B; Pike, Robert D; Bebout, Deborah C


    An unbranched N3O2 ligand 2,6-bis[((2-pyridinylmethyl)oxy)methyl]pyridine (L1) was used to prepare new mononuclear heteroleptic Group 12 perchlorate complexes characterized by IR, (1)H NMR and X-ray crystallography. Racemic complexes with pentadentate L1 and one to four oxygens from either water or perchlorate bound to a metal ion were structurally characterized. Octahedral [Zn(L1)(OH2)](ClO4)2 (1) and pentagonal bipyramidal [Cd(L1)(OH2)(OClO3)]ClO4 (2) structures were found with lighter congeners. The polymorphic forms of [Hg(L1)(ClO4)2] characterized (3 in P1[combining macron] and 4 in P21/c) had a mix of monodentate, anisobidentate and bidentate perchlorates, providing the first examples of a tricapped trigonal prismatic Hg(ii) coordination geometry, as well as additional examples of a rare square antiprismatic Hg(ii) coordination geometry. Solution state (1)H NMR characterization of the Group 12 complexes in CD3CN indicated intramolecular reorganization remained rapid under conditions where intermolecular M-L1 exchange was slow on the chemical shift time scale for Zn(ii) and on the J(M(1)H) time scale for Cd(ii) and Hg(ii). Solution studies with more than one equivalent of ligand also suggested that a complex with a 1 : 2 ratio of M : L1 contributed significantly to solution equilibria with Hg(ii) but not the other metal ions. The behavior of related linear pentadentate ligands with Group 12 perchlorate salts is discussed.

  19. Anaerobic ammonium oxidation in traditional municipal wastewater treatment plants with low-strength ammonium loading: Widespread but overlooked. (United States)

    Wang, Shanyun; Peng, Yongzhen; Ma, Bin; Wang, Shuying; Zhu, Guibing


    Occurrence of anaerobic ammonium oxidation (anammox) in marine and freshwater systems has greatly changed our understanding of global nitrogen (N) cycle and promoted the investigation of the role and ecological features of anammox in anthropogenic ecosystems. This study focused on the spatio-temporal abundance, activity, and biodiversity of anammox bacteria in full-scale municipal wastewater treatment plants (WWTPs) via traditional nitrification/denitrification route with low-strength ammonium loading. The anammox bacteria were detected in all the treatment units at the five WWTPs tested, even in aerobic zones (dissolved oxygen >2 mg L(-1)) with abundance of 10(5)-10(7) hydrazine synthase (hzs) gene copies g(-1). The (15)N-isotope tracing technology revealed that the anammox rates in WWTPs ranged from 0.08 to 0.36 μmol N g(-1) h(-1) in winter and 0.12-1.20 μmol N g(-1) h(-1) in summer with contributions of 2.05-6.86% and 1.71-7.26% to N2 production, respectively. The diversity of anammox bacteria in WWTPs was distributed over only two genera, Brocadia and Kuenenia. Additionally, the exploration of potential interspecies relationships indicated that ammonia oxidation bacteria (AOB) was the major nitrite-substrate producer for anammox during nitrification, while Nitrospira, a nitrite oxidation bacteria (NOB), was the potential major competitor for nitrite. These results suggested the contribution of N-removal by the widespread of anammox has been overlooked in traditional municipal WWTPs, and the ecological habitats of anammox bacteria in anthropogenic ecosystems are much more abundant than previously assumed.

  20. Determination of low levels of perchlorate in lettuce and spinach using ion chromatography-electrospray ionization mass spectrometry (IC-ESI-MS). (United States)

    Seyfferth, Angelia L; Parker, David R


    A sample preparation method was developed to quantify environmentally relevant (low micrograms per liter) concentrations of perchlorate (ClO4(-)) in leafy vegetables using IC-ESI-MS. Lettuce and spinach were macerated, centrifuged, and filtered, and the aqueous extracts were rendered water-clear using a one-step solid-phase extraction method. Total time for extraction and sample preparation was 6 h. Ion suppression was demonstrated and was likely due to unknown organics still present in the extract solution after cleanup. However, this interference was readily eliminated using a Cl(18)O4(-) internal standard at 1 microg/L in all standards and samples. Hydroponically grown perchlorate-free butterhead lettuce was spiked to either 10.3 or 37.7 microg/kg of fresh weight (FW), and recoveries were between 91 and 98% and between 93 and 101%, respectively. Five types of lettuce and spinach from a local grocery store were then analyzed; they contained from 0.6 to 6.4 microg/kg of FW. Spike recoveries using the store-bought samples ranged from 89 to 100%. The method detection limit for perchlorate in plant extracts is 40 ng/L, and the corresponding minimum reporting limit is 200 ng/L or 0.8 microg/kg of FW.