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Sample records for acids inorganic

  1. Ionisation constants of inorganic acids and bases in aqueous solution

    CERN Document Server

    Perrin, D D

    2013-01-01

    Ionisation Constants of Inorganic Acids and Bases in Aqueous Solution, Second Edition provides a compilation of tables that summarize relevant data recorded in the literature up to the end of 1980 for the ionization constants of inorganic acids and bases in aqueous solution. This book includes references to acidity functions for strong acids and bases, as well as details about the formation of polynuclear species. This text then explains the details of each column of the tables, wherein column 1 gives the name of the substance and the negative logarithm of the ionization constant and column 2

  2. Inorganic acid emission factors of semiconductor manufacturing processes.

    Science.gov (United States)

    Chein, HungMin; Chen, Tzu Ming; Aggarwal, Shankar Gopala; Tsai, Chuen-Jinn; Huang, Chun-Chao

    2004-02-01

    A huge amount of inorganic acids can be produced and emitted with waste gases from integrated circuit manufacturing processes such as cleaning and etching. Emission of inorganic acids from selected semiconductor factories was measured in this study. The sampling of the inorganic acids was based on the porous metal denuders, and samples were then analyzed by ion chromatography. The amount of chemical usage was adopted from the data that were reported to the Environmental Protection Bureau in Hsin-chu County according to the Taiwan Environmental Protection Agency regulation. The emission factor is defined as the emission rate (kg/month) divided by the amount of chemical usage (L/month). Emission factors of three inorganic acids (i.e., hydrofluoric acid [HF], hydrochloric acid [HCl], and sulfuric acid [H2SO4]) were estimated by the same method. The emission factors of HF and HCl were determined to be 0.0075 kg/L (coefficient of variation [CV] = 60.7%, n = 80) and 0.0096 kg/L (CV = 68.2%, n = 91), respectively. Linear regression equations are proposed to fit the data with correlation coefficient square (R2) = 0.82 and 0.9, respectively. The emission factor of H2SO4, which is in the droplet form, was determined to be 0.0016 kg/L (CV = 99.2%, n = 107), and its R2 was 0.84. The emission profiles of gaseous inorganic acids show that HF is the dominant chemical in most of the fabricators.

  3. Role of inorganic carbon in lactic acid bacteria metabolism

    OpenAIRE

    Arsène-Ploetze, Florence; Bringel, Françoise

    2004-01-01

    International audience; Capnophiles are bacteria stimulated by bicarbonate and CO$_2$, the two major forms of inorganic carbon (IC) in physiological neutral liquids. Capnophiles are often pathogenic heterotrophs found in IC-rich ecological niches such as human cavities. Like capnophiles, the growth of lactic acid bacteria (LAB) such as Lactobacillus plantarum and Enterococcus faecalis is stimulated by IC. CO$_2$ or HCO$^{-}_3$ are substrates in carbamoyl phosphate (CP) synthesis and other car...

  4. Effects of organic and inorganic acids on phosphorus release from municipal sludge.

    Science.gov (United States)

    Pakdil, N B; Filibeli, A

    2007-01-01

    This paper reports on the effects of inorganic acids (sulphuric acid, hydrochloric acid, nitric acid) and organic acids (citric acid, oxalic acids) for phosphorus recovery from sludge and struvite precipitation results. It was observed that both inorganic acid and organic acids were effective at phosphorus release. The studies on precipitation of released phosphorus from sludge as magnesium ammonium phosphate (struvite) were also done using nitric and oxalic acids. Phosphorus and heavy metals of leachate were analyzed before and after precipitation. It was observed that heavy metal concentrations in the extracted samples decrease after precipitation. Precipitation was accomplished by using extract derived with nitric acid; however, in oxalic acid applications, it was not achieved. When the chemical constituents of the dried material were examined oxygen, sodium and nitrogen were found to be the major elements.

  5. Water-free Alkaline Polymer-inorganic Acid Complexes with High Conductivity at Ambient Temperature

    Institute of Scientific and Technical Information of China (English)

    O.V.Chervakov; M.V.Andriianova; V.V.Riabenko; A.V.Markevich; E.M.Shembel; D.Meshri

    2007-01-01

    1 Results Recently increased interest is shown to proton conducting materials based on the alkaline polymer-inorganic acid complexes that is caused by a possibility of their application as the high-temperature electrolyte systems for various electrochemical devices (fuel cells,sensors,lithium power sources etc.).Complexes of inorganic acids with the alkaline polymers (polybenzimidazoles[1],polyvinylpyridines[2]) are characterized by high ionic conductivity at ambient temperatures (up to 10-2 Ω-1·cm-1) a...

  6. Proton conductivity of phosphoric acid doped polybenzimidazole and its composites with inorganic proton conductors

    DEFF Research Database (Denmark)

    He, Ronghuan; Qingfeng, Li; Gang, Xiao

    2003-01-01

    Phosphoric acid doped polybenzimidazole (PBI) and PBI composite membranes have been prepared in the present work. The PBI composites contain inorganic proton conductors including zirconium phosphate (ZrP), (Zr(HPO4)2·nH2O), phosphotungstic acid (PWA), (H3PW12O40·nH2O) and silicotungstic acid (Si...

  7. Proton conductivity of phosphoric acid doped polybenzimidazole and its composites with inorganic protontic conductors

    DEFF Research Database (Denmark)

    Li, Qingfeng

    2003-01-01

    contain inorganic protonic conductors including zirconium phosphate (ZrP), (Zr(HPO4)2. nH2O); phosphotungstic acid (PWA), (H3PW12O40. nH2O); and silicotungstic acid (SiWA), (H4SiW12O40 . nH2O). The conductivity of phosphoric acid doped PBI and PBI composite membranes was found to be dependent on the acid...

  8. Probing the interaction of individual amino acids with inorganic surfaces using atomic force spectroscopy.

    Science.gov (United States)

    Razvag, Yair; Gutkin, Vitaly; Reches, Meital

    2013-08-13

    This article describes single-molecule force spectroscopy measurements of the interaction between individual amino acid residues and inorganic surfaces in an aqueous solution. In each measurement, there is an amino acid residue, lysine, glutamate, phenylalanine, leucine, or glutamine, and each represents a class of amino acids (positively or negatively charged, aromatic, nonpolar, and polar). Force-distance curves measured the interaction of the individual amino acid bound to a silicon atomic force microscope (AFM) tip with a silcon substrate, cut from a single-crystal wafer, or mica. Using this method, we were able to measure low adhesion forces (below 300 pN) and could clearly determine the strength of interactions between the individual amino acid residues and the inorganic substrate. In addition, we observed how changes in the pH and ionic strength of the solution affected the adsorption of the residues to the substrates. Our results pinpoint the important role of hydrophobic interactions among the amino acids and the substrate, where hydrophobic phenylalanine exhibited the strongest adhesion to a silicon substrate. Additionally, electrostatic interactions also contributed to the adsorption of amino acid residues to inorganic substrates. A change in the pH or ionic strength values of the buffer altered the strength of interactions among the amino acids and the substrate. We concluded that the interplay between the hydrophobic forces and electrostatic interactions will determine the strength of adsorption among the amino acids and the surface. Overall, these results contribute to our understanding of the interaction at the organic-inorganic interface. These results may have implications for our perception of the specificity of peptide binding to inorganic surfaces. Consequently, it would possibly lead to a better design of composite materials and devices.

  9. Catalytic effects of inorganic acids on the decomposition of ammonium nitrate.

    Science.gov (United States)

    Sun, Jinhua; Sun, Zhanhui; Wang, Qingsong; Ding, Hui; Wang, Tong; Jiang, Chuansheng

    2005-12-09

    In order to evaluate the catalytic effects of inorganic acids on the decomposition of ammonium nitrate (AN), the heat releases of decomposition or reaction of pure AN and its mixtures with inorganic acids were analyzed by a heat flux calorimeter C80. Through the experiments, the different reaction mechanisms of AN and its mixtures were analyzed. The chemical reaction kinetic parameters such as reaction order, activation energy and frequency factor were calculated with the C80 experimental results for different samples. Based on these parameters and the thermal runaway models (Semenov and Frank-Kamenestkii model), the self-accelerating decomposition temperatures (SADTs) of AN and its mixtures were calculated and compared. The results show that the mixtures of AN with acid are more unsteady than pure AN. The AN decomposition reaction is catalyzed by acid. The calculated SADTs of AN mixtures with acid are much lower than that of pure AN.

  10. Joint effect of organic acids and inorganic salts on cloud droplet activation

    Directory of Open Access Journals (Sweden)

    M. Frosch

    2011-04-01

    Full Text Available We have investigated CCN properties of internally mixed particles composed of one organic acid (oxalic acid dihydrate, succinic acid, adipic acid, citric acid, cis-pinonic acid, or Nordic reference fulvic acid and one inorganic salt (sodium chloride or ammonium sulphate. Surface tension and water activity of aqueous model solutions with concentrations relevant for CCN activation were measured using a tensiometer and osmometry, respectively. The measurements were used to calculate Köhler curves and critical supersaturations, which were compared to measured critical supersaturations of particles with the same chemical compositions, determined with a cloud condensation nucleus counter. Surfactant surface partitioning was not accounted for. For the aqueous solutions containing cis-pinonic acid and fulvic acid, a depression of surface tension was observed, but for the remaining solutions the effect on surface tension was negligible at concentrations relevant for cloud droplet activation. The surface tension depression of aqueous solutions containing both organic acid and inorganic salt was approximately the same as or smaller than that of aqueous solutions containing the same mass of the corresponding pure organic acids. Water activity was found to be highly dependent on the type and amount of inorganic salt. Sodium chloride was able to decrease water activity more than ammonium sulphate and both inorganic salts are predicted to have a smaller Raoult term than the studied organic acids. Increasing the mass ratio of the inorganic salt led to a decrease in water activity. Water activity measurements were compared to results from the E-AIM model and values estimated from both constant and variable van't Hoff factors. The correspondence between measurements and estimates was overall good, except for highly concentrated solutions. Critical supersaturations calculated with Köhler theory based on measured water activity and surface tension, but not

  11. Effects of Inorganic acid catalysts on liquefaction of wood In phenol

    Institute of Scientific and Technical Information of China (English)

    Zhang Qiuhui; Zhao Guangjie; Chen Jinpeng

    2006-01-01

    In order to obtain the effects of acid catalysts on wood liquefaction in phenol, we investigated the liquefaction of wood powder from Chinese fir (Cunninghamia lanceolata) and poplar (Triploid Populus tomentosa Carr) in the presence of phenol with the following weak inorganic acids as catalysts: phosphoric acid (85%),sulfuric acid (36%),hydrochloric acid (37%)and oxalic acid (99.5%).Results show that phosphoric acid (85%) and sulfuric acid (36%) are better than the other catalysts.It was found that lower residue ratios can be obtained under defined reaction conditions: phenol/wood ratio is 4,a 10% catalyst based on the weight of phenol,a temperature of 150℃ for 2 h and phosphoric or sulfuric acid.The residue ratios are 3.2% and 4.0%,respectively.

  12. Photochemical alkylation of inorganic selenium in the presence of low molecular weight organic acids.

    Science.gov (United States)

    Guo, Xuming; Sturgeon, Ralph E; Mester, Zoltán; Gardner, Graeme J

    2003-12-15

    Using a flow-through photochemical reactor and a low pressure mercury lamp as a UV source, alkyl selenium species are formed from inorganic selenium(IV) in the presence of low molecular weight organic acids (LMW acids). The volatile alkyl Se species were cryogenically trapped and identified by GC-MS and GC-ICP-MS. In the presence of formic, acetic, propionic and malonic acids, inorganic selenium(IV) is converted by UV irradiation to volatile selenium hydride and carbonyl, dimethylselenide and diethylselenide, respectively. Se(IV) was successfully removed from contaminated agricultural drainage waters (California, U.S.A.) using a batch photoreactor system Se. Photochemical alkylation may thus offer a promising means of converting toxic selenium salts, present in contaminated water, to less toxic dimethylselenide. The LMW acids and photochemical alkylation process may also be key to understanding the source of atmospheric selenium and are likely involved in its mobility in the natural anaerobic environment.

  13. Joint effect of organic acids and inorganic salts on cloud droplet activation

    Directory of Open Access Journals (Sweden)

    M. Frosch

    2010-07-01

    Full Text Available We have investigated CCN properties of internally mixed particles composed of one organic acid (oxalic acid, succinic acid, adipic acid, citric acid, cis-pinonic acid, or nordic reference fulvic acid and one inorganic salt (sodium chloride or ammonium sulphate. Surface tension and water activity of aqueous model solutions with concentrations relevant for CCN activation were measured using a tensiometer and osmometry, respectively. The measurements were used to calculate Köhler curves, which were compared to measured critical supersaturations of particles with the same chemical compositions, determined with a cloud condensation nucleus counter. Surfactant surface partitioning was not accounted for. For the mixtures containing cis-pinonic acid or fulvic acid, a depression of surface tension was observed, but for the remaining mixtures the effect on surface tension was negligle at concentrations relevant for cloud droplet activation, and water activity was the more significant term in the Köhler equation. The surface tension depression of aqueous solutions containing both organic acid and inorganic salt was approximately the same as or smaller than that of aqueous solutions containing the same mass of the corresponding pure organic acids. Water activity was found to be highly dependent on the type and amount of inorganic salt. Sodium chloride was able to decrease water activity more than ammonium sulphate and both inorganic compounds had a higher effect on water activity than the studied organic acids, and increasing the mass ratio of the inorganic compound led to a decrease in water activity. Water activity measurements were compared to results from the E-AIM model and values estimated from both constant and variable van't Hoff factors to evaluate the performance of these approaches. The correspondence between measuments and estimates was overall good, except for highly concentrated solutions. Critical supersaturations calculated with K

  14. Effect of dietary phytic acid and inorganic iron on the quality of chilled pork.

    Directory of Open Access Journals (Sweden)

    Renilda Terezinha Monteiro

    2015-09-01

    Full Text Available The objective of this study was to evaluate the effect of supplementing inorganic iron and phytic acid to the diet for finishing pigs on meat quality after 24 hours and 7 days of refrigeration. Forty castrated male finishing pigs of a commercial genotype, with an initial mean weight of 64.34 ± 6.64 kg and age of 108 days, were used. The animals were weighed and housed individually in brick pens with an area of three m2 and compact floor, receiving water and ration ad libitum for 30 days. A randomized block design in a 2 x 2 factorial scheme was used, corresponding to diets supplemented or not with inorganic iron and with two levels of phytic acid, high (4.85% and low (2.98%. The animals were slaughtered when they had reached a mean weight of 100.76 ± 6.54 kg and longissimus dorsi muscle samples were collected for the analysis of meat quality. The following parameters were analyzed in the samples: pH, color, marbling, water loss through pressure, shear force, iron composition, and lipid oxidation. No differences in the variables analyzed were observed between factors, except for muscle iron concentration, which was higher for the diet with inclusion of inorganic iron. Lipid oxidation was not influenced by the presence or absence of phytic acid and inorganic iron. The results show that diets with elevated phytic acid levels supplemented or not with inorganic iron can be used for finishing pigs without compromising meat quality during the refrigeration phase.

  15. Elevational Variation in Soil Amino Acid and Inorganic Nitrogen Concentrations in Taibai Mountain, China.

    Directory of Open Access Journals (Sweden)

    Xiaochuang Cao

    Full Text Available Amino acids are important sources of soil organic nitrogen (N, which is essential for plant nutrition, but detailed information about which amino acids predominant and whether amino acid composition varies with elevation is lacking. In this study, we hypothesized that the concentrations of amino acids in soil would increase and their composition would vary along the elevational gradient of Taibai Mountain, as plant-derived organic matter accumulated and N mineralization and microbial immobilization of amino acids slowed with reduced soil temperature. Results showed that the concentrations of soil extractable total N, extractable organic N and amino acids significantly increased with elevation due to the accumulation of soil organic matter and the greater N content. Soil extractable organic N concentration was significantly greater than that of the extractable inorganic N (NO3--N + NH4+-N. On average, soil adsorbed amino acid concentration was approximately 5-fold greater than that of the free amino acids, which indicates that adsorbed amino acids extracted with the strong salt solution likely represent a potential source for the replenishment of free amino acids. We found no appreciable evidence to suggest that amino acids with simple molecular structure were dominant at low elevations, whereas amino acids with high molecular weight and complex aromatic structure dominated the high elevations. Across the elevational gradient, the amino acid pool was dominated by alanine, aspartic acid, glycine, glutamic acid, histidine, serine and threonine. These seven amino acids accounted for approximately 68.9% of the total hydrolyzable amino acid pool. The proportions of isoleucine, tyrosine and methionine varied with elevation, while soil major amino acid composition (including alanine, arginine, aspartic acid, glycine, histidine, leucine, phenylalanine, serine, threonine and valine did not vary appreciably with elevation (p>0.10. The compositional

  16. Interactions between uptake of amino acids and inorganic nitrogen in wheat plants

    Directory of Open Access Journals (Sweden)

    E. Gioseffi

    2012-04-01

    Full Text Available Soil-borne amino acids may constitute a source of nitrogen (N for plants in various terrestrial ecosystems but their importance for total N nutrition is unclear, particularly in nutrient-rich arable soils. One reason for this uncertainty is lack of information on how the absorption of amino acids by plant roots is affected by the simultaneous presence of inorganic N forms. The objective of the present study was to study absorption of glycine (Gly and glutamine (Gln by wheat roots and their interactions with nitrate (NO3 and ammonium (NH4+ during uptake. The underlying hypothesis was that amino acids, when present in nutrient solution together with inorganic N, may lead to down-regulation of the inorganic N uptake, thereby resulting in similar total N uptake rates. Amino acids were enriched with double-labelled 15N and 13C, while NO3 and NH4+ acquisition was determined by their rate of removal from the nutrient solution surrounding the roots. The uptake rates of NO3 and NH4+ did not differ from each other and were generally about twice as high as the uptake rate of organic N when the different N forms were supplied separately in concentrations of 2 mM. Nevertheless, replacement of 50% of the inorganic N with organic N was able to restore the N uptake to the same level as that in the presence of only inorganic N. Co-provision of NO3 did not affect glycine uptake, while the presence of glycine down-regulated NO3 uptake. The ratio between 13C and 15N were lower in shoots than in roots and also lower than the theoretical values, reflecting higher C losses via respiratory processes compared to N losses. It is concluded that organic N can constitute a significant N-source for wheat plants and that there is an interaction

  17. Safety Assessment of Citric Acid, Inorganic Citrate Salts, and Alkyl Citrate Esters as Used in Cosmetics.

    Science.gov (United States)

    Fiume, Monice M; Heldreth, Bart A; Bergfeld, Wilma F; Belsito, Donald V; Hill, Ronald A; Klaassen, Curtis D; Liebler, Daniel C; Marks, James G; Shank, Ronald C; Slaga, Thomas J; Snyder, Paul W; Andersen, F Alan

    2014-05-26

    The CIR Expert Panel (Panel) assessed the safety of citric acid, 12 inorganic citrate salts, and 20 alkyl citrate esters as used in cosmetics, concluding that these ingredients are safe in the present practices of use and concentration. Citric acid is reported to function as a pH adjuster, chelating agent, or fragrance ingredient. Some of the salts are also reported to function as chelating agents, and a number of the citrates are reported to function as skin-conditioning agents but other functions are also reported. The Panel reviewed available animal and clinical data, but because citric acid, calcium citrate, ferric citrate, manganese citrate, potassium citrate, sodium citrate, diammonium citrate, isopropyl citrate, stearyl citrate, and triethyl citrate are generally recognized as safe direct food additives, dermal exposure was the focus for these ingredients in this cosmetic ingredient safety assessment.

  18. Freezing-Enhanced Dissolution of Iron Oxides: Effects of Inorganic Acid Anions.

    Science.gov (United States)

    Jeong, Daun; Kim, Kitae; Min, Dae Wi; Choi, Wonyong

    2015-11-03

    Dissolution of iron from mineral dust particles greatly depends upon the type and amount of copresent inorganic anions. In this study, we investigated the roles of sulfate, chloride, nitrate, and perchlorate on the dissolution of maghemite and lepidocrocite in ice under both dark and UV irradiation and compared the results with those of their aqueous counterparts. After 96 h of reaction, the total dissolved iron in ice (pH 3 before freezing) was higher than that in the aqueous phase (pH 3) by 6-28 times and 10-20 times under dark and UV irradiation, respectively. Sulfuric acid was the most efficient in producing labile iron under dark condition, whereas hydrochloric acid induced the most dissolution of the total and ferrous iron in the presence of light. This ice-induced dissolution result was also confirmed with Arizona Test Dust (AZTD). In the freeze-thaw cycling test, the iron oxide samples containing chloride, nitrate, or perchlorate showed a similar extent of total dissolved iron after each cycling while the sulfate-containing sample rapidly lost its dissolution activity with repeating the cycle. This unique phenomenon observed in ice might be related to the freeze concentration of protons, iron oxides, and inorganic anions in the liquid-like ice grain boundary region. These results suggest that the ice-enhanced dissolution of iron oxides can be a potential source of bioavailable iron, and the acid anions critically influence this process.

  19. Organic acids and inorganic anions in Bayer liquors by ion chromatography after solid-phase extraction

    Institute of Scientific and Technical Information of China (English)

    ZHONG Fu-jin; CHEN Xiao-qing; ZHANG Shu-chao; LI Yue-ping

    2007-01-01

    A method for the simultaneous separation and determination of organic acids and inorganic anions in Bayer liquors was developed by gradient ion chromatography with suppressed conductivity detection. Formate, acetate, propionate, oxalate, succinate,glutarate, fluoride, chloride and sulfate were separated and determined in 33 min. The samples were pretreated with solid-phase extraction, which has high selectivity for removing a large number of metallic ions in the Bayer liquors, and filtered with a 0.45 μm filter membrane before being injected into the ion chromatographic system. The separation of six organic acids and three inorganic anions was achieved on an IonPac AS11-HC column with KOH as the eluent, and the detection was performed by a conductivity detection mode. No interference is found in the presence of fluorate, chlorate and sulphate when organic acids are determined. The calibration graphs of peak area for all the analytes are linear over a wide range. The relative standard derivation of the peak area of analytes is less than 2.14%. Under optimum conditions the detection ranges from 0.2 to 100.0 mg/L. The average recoveries of the added standards are between 94.3% and 102.8%.

  20. Application of a Non-thermal Atmospheric Pressure Plasma Jet to the Decomposition of Salicylic Acid to Inorganic Carbon

    OpenAIRE

    Kuroda, Kosuke; Ishijima, Tatsuo; Kaga, Toshiki; Shiomomura, Kai; Ninomiya, Kazuaki; Takahashi, Kenji

    2015-01-01

    A non-thermal atmospheric pressure plasma jet technique was applied to decompose salicylic acid to inorganic carbon. Excess hydroxyl radical, which has a high oxidation potential, decomposed salicylic acid within 10 min, and total organic carbon decreased to 20% after 30 min. © 2015 The Chemical Society of Japan.

  1. [Determination of organic acids and inorganic anions by gradient ion chromatography].

    Science.gov (United States)

    Liu, Z; Liu, K; Shen, D; Song, Q; Mou, S; Feng, Y

    1997-07-01

    The chromatographic conditions for separation and detection of organic acids and inorganic anions by gradient ion chromatography with suppressed conductivity detection were studied. The optimized gradient programs were established. Ion chromatography were performed with a DX-100 chromatograph (DIONEX). The separation column is IonPac-AS11. Compared with NaHCO3/Na2CO3 and Na2B4O7, NaOH was the optimal eluent. The effect of organic modifier was also studied. Among methanol, 2-propanol and acetonitrile, methanol can make ion pairs such as malate and succinate, malonate and tartrate gaining baseline resolution. By using ion exchange separation, Cl-, NO3-, malate, succinate, malonate, tartrate, SO4(2-), oxalate were eluted between 5 mmol/L NaOH-16% CH3OH and 10 mmol/L NaOH-16% CH3OH in 25 min. A mobile phase composed of 30 mmol/L NaOH, 50% CH3OH and D.I. water was chosen to elute two groups of organic acids and inorganic anions: (1) quinate, formate, Cl-, malate, malonate, oxalate, citrate, isocitrate, aconitate; (2) lactate, Cl-, SO4(2-), tartrate, PO4(3-), citrate, isocitrate, aconitate. The detection limits (S/N = 3) were 0.1625 (quinate), 0.0691 (formate), 0.0115 (Cl-), 0.0886 (malate), 0.0591 (malonate), 0.0263 (oxalate), 0.1147 (citrate), 0.2017 (isocitrate), 0.3656 (cis-aconitate), 0.1045 (trans-aconitate), 0.1950 (lactate), 0.0729 (tartrate), 0.0224 (SO4(2-)) and 0.0692 (PO4(3-)) mg/L. The relative standard deviations were lower than 11.9% (n = 7) and the correlation coefficients ranged from 0.9212 for Cl- to 0.9999 for formate. The method was applied to determine the organic acids and inorganic anions of beverages and citric acids fermenting-medium. The results were satisfactory.

  2. Carborane acids. New "strong yet gentle" acids for organic and inorganic chemistry.

    Science.gov (United States)

    Reed, Christopher A

    2005-04-07

    Icosahedral carborane anions such as CHB11Cl11- are amongst the least coordinating, most chemically inert anions known. They are also amongst the least basic, so their conjugate acids, H(carborane), are superacids (i.e. stronger than 100% H2SO4). Acidity scale measurements indicate that H(CHB11Cl11) is the strongest pure Brønsted acid presently known, surpassing triflic and fluorosulfuric acid. Nevertheless, it is also an extremely gentle acid--because its conjugate base engages in so little chemistry. Carborane acids separate protic acidity from anion nucleophilicity and destructive oxidative capacity in the conjugate base, to a degree not previously achieved. As a result, many long-sought, highly acidic, reactive cations such as protonated benzene (C6H7+), protonated C60(HC60+), tertiary carbocations (R3C+), vinyl cations (R2C=C(+)-R), silylium ions (R3Si+) and discrete hydronium ions (H3O+, H5O2+ etc.) can be readily isolated as carborane salts and characterized at room temperature by X-ray crystallography.

  3. SYNTHESIS OF MESOPOROUS TiO2 MATERIALS WITH HIGH SPECIFIC AREA USING INORGANIC ACIDS AS CATALYSTS

    Institute of Scientific and Technical Information of China (English)

    Dan Huang; Guangsheng Luo; Liming Yang; Yujun Wang

    2005-01-01

    This paper presents a synthesis process for preparing mesoporous titanium dioxide materials in the absence of any templates and using inorganic acids as catalysts. Tetrabutyl titanate was used as the precursor at ambient temperature, and four different inorganic acids, i.e., hydrochloric, nitric, sulfuric and phosphoric, were used as catalysts.The as-prepared mesoporous TiO2 materials were characterized by SEM, XRD and nitrogen adsorption/desorption measurements. The influences of different inorganic acids on the properties of TiO2 were discussed and compared in details. Experiments showed that the inorganic acids have significant effects on the surface area, pore volume, pore size,and pore size distribution of the products. The mesoporous TiO2 materials catalyzed by phosphoric acid exhibited the largest specific surface area and largest pore volume with narrow pore size distribution. Vacuum and infrared drying methods tested in the process were found to have subtle impact on the structure of the TiO2 materials prepared.

  4. The presence of amino acids affects inorganic N uptake in non-mycorrhizal seedlings of European beech (Fagus sylvatica).

    Science.gov (United States)

    Stoelken, Gunda; Simon, Judy; Ehlting, Barbara; Rennenberg, Heinz

    2010-09-01

    To investigate the impact of organic N compounds for inorganic nitrogen uptake in the rhizosphere, we fed ammonium nitrate with or without amino acids (i.e., glutamine or arginine) to the roots of non-mycorrhizal beech (Fagus sylvatica L.) seedlings under controlled conditions at different levels of N availability. Uptake of individual N sources was determined from ¹⁵N (inorganic N) and ¹⁵N ¹³C (organic N) accumulation in the roots. In addition, gene fragments encoding proteins involved in N uptake and metabolism were cloned from beech for gene expression analyses by quantitative real-time PCR in the roots. Generally, ammonium was preferred over nitrate as N source. Organic N sources were taken up by beech roots as intact molecules. Uptake of organic N was significantly higher than inorganic N uptake, thus contributing significantly to N nutrition of beech. Depending on the level of N availability, inorganic N uptake was negatively affected by the presence of organic N sources. This result indicates an overestimation of the contribution of inorganic N uptake to N nutrition of beech in previous studies. Apparently, association with mycorrhizal fungi is not essential for organic N uptake by beech roots. Gene expression analyses showed that transcriptional regulation of the amino acid transporters FsCAT3, FsCAT5, FsAAT and FsAAP and the ammonium transporter FsAMT1.2 in the roots is involved in N nutrition of beech.

  5. Analysis of trace inorganic anions in weak acid salts by single pump cycling-column-switching ion chromatography.

    Science.gov (United States)

    Huang, Zhongping; Ni, Chengzhu; Zhu, Zhuyi; Pan, Zaifa; Wang, Lili; Zhu, Yan

    2015-05-01

    The application of ion chromatography with the single pump cycling-column-switching technique was described for the analysis of trace inorganic anions in weak acid salts within a single run. Due to the hydrogen ions provided by an anion suppressor electrolyzing water, weak acid anions could be transformed into weak acids, existing as molecules, after passing through the suppressor. Therefore, an anion suppressor and ion-exclusion column were adopted to achieve on-line matrix elimination of weak acid anions with high concentration for the analysis of trace inorganic anions in weak acid salts. A series of standard solutions consisting of target anions of various concentrations from 0.005 to 10 mg/L were analyzed, with correlation coefficients r ≥ 0.9990. The limits of detection were in the range of 0.67 to 1.51 μg/L, based on the signal-to-noise ratio of 3 and a 25 μL injection volume. Relative standard deviations for retention time, peak area, and peak height were all less than 2.01%. A spiking study was performed with satisfactory recoveries between 90.3 and 104.4% for all anions. The chromatographic system was successfully applied to the analysis of trace inorganic anions in five weak acid salts.

  6. Ambient cure polyimide foams prepared from aromatic polyisocyanates, aromatic polycarboxylic compounds, furfuryl alcohol, and a strong inorganic acid

    Science.gov (United States)

    Sawko, Paul M. (Inventor); Riccitiello, Salvatore R. (Inventor); Hamermesh, Charles L. (Inventor)

    1980-01-01

    Flame and temperature resistant polyimide foams are prepared by the reaction of an aromatic dianhydride, e.g., pyromellitic dianhydride, with an aromatic polyisocyanate, e.g., polymethylene polyphenylisocyanate (PAPI) in the presence of an inorganic acid and a lower molecular weight alcohol, e.g., dilute sulfuric acid or phosphoric acid and furfuryl alcohol. The exothermic reaction between the acid and the alcohol provides the heat necessary for the other reactants to polymerize without the application of any external heat. Such mixtures, therefore, are ideally suited for in situ foam formation, especially where the application of heat is not practical or possible.

  7. Compensation of inorganic acid interferences in ICP-OES and ICP-MS using a Flow Blurring® multinebulizer

    OpenAIRE

    Aguirre Pastor, Miguel Ángel; Fialhob, Lucimar L.; NÓBREGA, Joaquim A.; Hidalgo Núñez, Montserrat; Canals Hernández, Antonio

    2014-01-01

    A new and easy method has been proposed for compensation of inorganic acid matrix effects in ICP-OES and ICP-MS. The method consists on an on-line standard addition calibration using a Flow Blurring® multinebulizer (FBMN-based system). Experimental conditions of the FBMN-based system are optimized for both ICP-OES and ICP-MS. Under optimized conditions recovery values obtained in the analysis of synthetic acid samples were close to 100% for HNO3 and HCl (with acid concentrations of up to 15% ...

  8. Reactions between Criegee Intermediates and the Inorganic Acids HCl and HNO3 : Kinetics and Atmospheric Implications.

    Science.gov (United States)

    Foreman, Elizabeth S; Kapnas, Kara M; Murray, Craig

    2016-08-22

    Criegee intermediates (CIs) are a class of reactive radicals that are thought to play a key role in atmospheric chemistry through reactions with trace species that can lead to aerosol particle formation. Recent work has suggested that water vapor is likely to be the dominant sink for some CIs, although reactions with trace species that are sufficiently rapid can be locally competitive. Herein, we use broadband transient absorption spectroscopy to measure rate constants for the reactions of the simplest CI, CH2 OO, with two inorganic acids, HCl and HNO3 , both of which are present in polluted urban atmospheres. Both reactions are fast; at 295 K, the reactions of CH2 OO with HCl and HNO3 have rate constants of 4.6×10(-11)  cm(3)  s(-1) and 5.4×10(-10)  cm(3)  s(-1) , respectively. Complementary quantum-chemical calculations show that these reactions form substituted hydroperoxides with no energy barrier. The results suggest that reactions of CIs with HNO3 in particular are likely to be competitive with those with water vapor in polluted urban areas under conditions of modest relative humidity.

  9. Effects of Inorganic Fillers on the Thermal and Mechanical Properties of Poly(lactic acid

    Directory of Open Access Journals (Sweden)

    Xingxun Liu

    2014-01-01

    Full Text Available Addition of filler to polylactic acid (PLA may affect its crystallization behavior and mechanical properties. The effects of talc and hydroxyapatite (HA on the thermal and mechanical properties of two types of PLA (one amorphous and one semicrystalline have been investigated. The composites were prepared by melt blending followed by injection molding. The molecular weight, morphology, mechanical properties, and thermal properties have been characterized by gel permeation chromatography (GPC, scanning electron microscope (SEM, instron tensile tester, thermogravimetric analysis (TGA, differential scanning calorimetry (DSC, and dynamic mechanical analysis (DMA. It was found that the melting blending led to homogeneous distribution of the inorganic filler within the PLA matrix but decreased the molecular weight of PLA. Regarding the filler, addition of talc increased the crystallinity of PLA, but HA decreased the crystallinity of PLA. The tensile strength of the composites depended on the crystallinity of PLA and the interfacial properties between PLA and the filler, but both talc and HA filler increased the toughness of PLA.

  10. Photochemical production of dissolved inorganic carbon from suwannee river humic acid

    Institute of Scientific and Technical Information of China (English)

    WANG Xuejun; LOU Tao; XIE Huixiang

    2009-01-01

    The photochemical mineralization of dissolved organic carbon (DOC) to dissolved inorganic carbon (DIC) is a key process in carbon cycling. Using a Suntest CPS solar simulator, Suwannee River humic acid (SRHA) was photooxidated to examine the effects of O2 levels, the wavelength of incident light, and the concentration of Fe on the photoproduction of DIC. Increasing the O2 abundance enhanced photodegradation of SRHA. The rate of DIC photoproduction under air saturation in the first 24 h (4.40 μmol/(L h)) was increased by a factor of 1.56 under O2 saturation, but fell by only 36% under N2 saturation. To evaluate the relative importance of UV-B, UV-A, and visible radiation in the photodegradation, we examined the above process using Mylar-d films and UF-3 and UF-4 plexiglass filters. The results indicated that the UV-B, UV-A and visible wavelengths accounted for 31.8%, 32.6% and 25.6%, respectively, of DIC production with simulated sunlight irradiation. The above results also indicated that photoproduction of DIC could take place in natural water at depths greater than those that UV light can reach. When 20 μmol/L desferrioxamine mesylate (DFOM, a strong Fe complexing ligand) was added, the rate of DIC photoproduction fell to 55.6% that of the original SRHA samples with 5.46 μmol/L Fe.

  11. Docosahexaenoic acid counteracts attenuation of CD95-induced cell death by inorganic mercury

    Energy Technology Data Exchange (ETDEWEB)

    Gill, Randall [Department of Immunology and Microbiology, Wayne State University, Detroit MI (United States); Lanni, Lydia; Jen, K.-L. Catherine [Department of Nutrition and Food Science, Wayne State University, Detroit MI (United States); McCabe, Michael J. [Department of Environmental Medicine, University of Rochester, Rochester NY (United States); Rosenspire, Allen, E-mail: arosenspire@wayne.edu [Department of Immunology and Microbiology, Wayne State University, Detroit MI (United States)

    2015-01-01

    In the United States the principal environmental exposure to mercury is through dietary consumption of sea food. Although the mechanism by which low levels of mercury affect the nervous system is not well established, epidemiological studies suggest that low level exposure of pregnant women to dietary mercury can adversely impact cognitive development in their children, but that Docosahexaenoic acid (DHA), the most prominent n-polyunsaturated fatty acid (n-PUFA) present in fish may counteract negative effects of mercury on the nervous system. Aside from effects on the nervous system, epidemiological and animal studies have also suggested that low level mercury exposure may be a risk factor for autoimmune disease. However unlike the nervous system where a mechanism linking mercury to impaired cognitive development remains elusive, we have previously suggested a potential mechanism linking low level mercury exposures to immune system dysfunction and autoimmunity. In the immune system it is well established that disruption of CD95 mediated apoptosis leads to autoimmune disease. We have previously shown in vitro as well as in vivo that in lymphocytes burdened with low levels of mercury, CD95 mediated cell death is impaired. In this report we now show that DHA counteracts the negative effect of mercury on CD95 signaling in T lymphocytes. T cells which have been pre-exposed to DHA are able to cleave pro-caspase 3 and efficiently signal programmed cell death through the CD95 signaling pathway, whether or not they are burdened with low levels of mercury. Thus DHA may lower the risk of autoimmune disease after low level mercury exposures. - Highlights: • Inorganic mercury (Hg{sup 2+}) interferes with CD95 mediated cell death in Jurkat T cells • DHA restores the ability of CD95 to signal cell death in Hg{sup 2+} intoxicated T cells • The restoration of CD95 mediated cell death by DHA is correlated with increased activation of Caspase 3.

  12. Correlations between the contents of phytic acid and inorganic phosphorous and downy mildew resistance of corn inbred lines

    OpenAIRE

    Pantipa Na Chiangmai*; Phrutiya Nilprapruck; Warapon Bunkoed; Phakatip Yodmingkhwan; Chokechai Aekatasanawan; Mana Kanjanamaneesathian

    2015-01-01

    Seeds of corn inbred lines collected at the National Corn and Sorghum Research Center (NCSRC), Kasetsart University, were analyzed to determine the contents of phytic acid (PA) and inorganic phosphorous (InP). These 28 and 29 inbred lines were cultivated at the NCSRC (in the 2008 late rainy season and 2009 early rainy season) to evaluate their resistance to corn downy mildew caused by Peronosclerospora sorghi. Results showed that the values of the PA, InP contents and downy mildew...

  13. 3D Polyaniline Architecture by Concurrent Inorganic and Organic Acid Doping for Superior and Robust High Rate Supercapacitor Performance

    Science.gov (United States)

    Gawli, Yogesh; Banerjee, Abhik; Dhakras, Dipti; Deo, Meenal; Bulani, Dinesh; Wadgaonkar, Prakash; Shelke, Manjusha; Ogale, Satishchandra

    2016-02-01

    A good high rate supercapacitor performance requires a fine control of morphological (surface area and pore size distribution) and electrical properties of the electrode materials. Polyaniline (PANI) is an interesting material in supercapacitor context because it stores energy Faradaically. However in conventional inorganic (e.g. HCl) acid doping, the conductivity is high but the morphological features are undesirable. On the other hand, in weak organic acid (e.g. phytic acid) doping, interesting and desirable 3D connected morphological features are attained but the conductivity is poorer. Here the synergy of the positive quality factors of these two acid doping approaches is realized by concurrent and optimized strong-inorganic (HCl) and weak-organic (phytic) acid doping, resulting in a molecular composite material that renders impressive and robust supercapacitor performance. Thus, a nearly constant high specific capacitance of 350 F g‑1 is realized for the optimised case of binary doping over the entire range of 1 A g‑1 to 40 A g‑1 with stability of 500 cycles at 40 A g‑1. Frequency dependant conductivity measurements show that the optimized co-doped case is more metallic than separately doped materials. This transport property emanates from the unique 3D single molecular character of such system.

  14. 3D Polyaniline Architecture by Concurrent Inorganic and Organic Acid Doping for Superior and Robust High Rate Supercapacitor Performance.

    Science.gov (United States)

    Gawli, Yogesh; Banerjee, Abhik; Dhakras, Dipti; Deo, Meenal; Bulani, Dinesh; Wadgaonkar, Prakash; Shelke, Manjusha; Ogale, Satishchandra

    2016-02-12

    A good high rate supercapacitor performance requires a fine control of morphological (surface area and pore size distribution) and electrical properties of the electrode materials. Polyaniline (PANI) is an interesting material in supercapacitor context because it stores energy Faradaically. However in conventional inorganic (e.g. HCl) acid doping, the conductivity is high but the morphological features are undesirable. On the other hand, in weak organic acid (e.g. phytic acid) doping, interesting and desirable 3D connected morphological features are attained but the conductivity is poorer. Here the synergy of the positive quality factors of these two acid doping approaches is realized by concurrent and optimized strong-inorganic (HCl) and weak-organic (phytic) acid doping, resulting in a molecular composite material that renders impressive and robust supercapacitor performance. Thus, a nearly constant high specific capacitance of 350 F g(-1) is realized for the optimised case of binary doping over the entire range of 1 A g(-1) to 40 A g(-1) with stability of 500 cycles at 40 A g(-1). Frequency dependant conductivity measurements show that the optimized co-doped case is more metallic than separately doped materials. This transport property emanates from the unique 3D single molecular character of such system.

  15. HPLC inorganic arsenic speciation analysis of samples containing high sulfuric acid and iron levels

    NARCIS (Netherlands)

    Gonzalez-Contreras, P.A.; Gerrits, I.P.A.M.; Weijma, J.; Buisman, C.J.N.

    2011-01-01

    To monitor the oxidation of arsenite to arsenate in oxidizing and bioleaching reactors, speciation analysis of the inorganic arsenic compounds is required. Existing arsenic speciation analysis techniques are based on the use of liquid chromatography columns coupled to detector equipment such as indu

  16. Insights into the Interactions of Amino Acids and Peptides with Inorganic Materials Using Single-Molecule Force Spectroscopy.

    Science.gov (United States)

    Das, Priyadip; Duanias-Assaf, Tal; Reches, Meital

    2017-03-06

    The interactions between proteins or peptides and inorganic materials lead to several interesting processes. For example, combining proteins with minerals leads to the formation of composite materials with unique properties. In addition, the undesirable process of biofouling is initiated by the adsorption of biomolecules, mainly proteins, on surfaces. This organic layer is an adhesion layer for bacteria and allows them to interact with the surface. Understanding the fundamental forces that govern the interactions at the organic-inorganic interface is therefore important for many areas of research and could lead to the design of new materials for optical, mechanical and biomedical applications. This paper demonstrates a single-molecule force spectroscopy technique that utilizes an AFM to measure the adhesion force between either peptides or amino acids and well-defined inorganic surfaces. This technique involves a protocol for attaching the biomolecule to the AFM tip through a covalent flexible linker and single-molecule force spectroscopy measurements by atomic force microscope. In addition, an analysis of these measurements is included.

  17. Validation study of a rapid colorimetric method for the determination of phytic acid and inorganic phosphorus from seeds

    Directory of Open Access Journals (Sweden)

    Dragičević Vesna D.

    2011-01-01

    Full Text Available Phytate, as an important mineral storage compound in seeds, is vital for seed/grain development; it is often considered to be an antinutritional substance. The objective of this study was to develop a rapid and inexpensive colorimetric method of measuring phytate and inorganic P (Pi concentrations from maize, soybean and sunflower seed/grain extracts, by combining adequate precision and simplicity, ideal for breeders interested in improving simultaneously Pi and phytate levels. The investigated extraction mediums: double distilled (DD H2O, 2.4 % HCl and 5 % trichloracetic acid (TCA were proved to be suitable for the analysis of phytic acid and inorganic phosphorus in seed extracts. The advantages of 5 % TCA over to DD H2O and 2.4 % HCl were reflected through the low limit of detection for both phytic acid and Pi and good recovery with low bias. A low detection limit for Pi is important for samples with naturally low Pi concentrations, such as soybean seeds.

  18. Synthesis, crystal structure and properties of inorganic-organic hybrid polymers based on 8-hydroxylquinoline-5-sulfonic acid

    Institute of Scientific and Technical Information of China (English)

    WANG Ying; XUE Ming; XU JiaNing; ZHU GuangShan; QIU ShiLun

    2009-01-01

    Two new inorganic-organic hybrid polymers, Mn(QS)(H_2O) (1) and Co(QS)(H_2O)2 (2) (H2QS=8-hydroxylquinoline-5-sulfonic acid), based on 8-hydroxylquinoline-5-sulfonate ligand, have been synthesized under solvothermal conditions and their structures were solved by single-crystal X-ray diffraction analysis. Compound 1 is a three-dimensional open framework with rutile topology structure, and compound 2 is a three-dimensional supramolecular structure. These compounds were characterized by powder XRD, infrared spectroscopy, thermogravimetric analysis, fluorescence properties and magnetism properties.

  19. Synthesis,crystal structure and properties of inorganic-organic hybrid polymers based on 8-hydroxylquinoline-5-sulfonic acid

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Two new inorganic-organic hybrid polymers, Mn(QS)(H2O) (1) and Co(QS)(H2O)2 (2) (H2QS=8-hydroxyl-quinoline-5-sulfonic acid), based on 8-hydroxylquinoline-5-sulfonate ligand, have been synthesized under solvothermal conditions and their structures were solved by single-crystal X-ray diffraction analysis. Compound 1 is a three-dimensional open framework with rutile topology structure, and compound 2 is a three-dimensional supramolecular structure. These compounds were characterized by powder XRD, infrared spectroscopy, thermogravimetric analysis, fluorescence properties and magnetism properties.

  20. Organic-inorganic hybrid protonic polymeric electrolytes grafted by sulfonic acid/sulfonamide moieties

    Energy Technology Data Exchange (ETDEWEB)

    Depre, L.; Poinsignon, C.; Popall, M.

    2000-07-01

    Thin proton conducting membranes of an organic-inorganic polymer electrolyte bearing sulphonamide and sulfonic groups are prepared by sol-gel process. Polycondensation of alkoxysilanes provides the inorganic silicate backbone whereas the organic network is formed from reactive functional groups R{prime}(({minus}DH{sub 2}){sub 3}-SO{sub 3}H) and [({minus}CH{sub 2}){sub 3}-SO{sub 2}NH{sub 2}] of alkoxysilanes of R{prime}Si[OR{sub 3}] type. Proton conductivity measured in the dry and wet state under controlled Temperature and Relative Humidity increases from 10{sup {minus}4} S/cm under vacuum to 6 10{sup {minus}2} S/cm at 70 C and 96% RH. Conductivity dependence on temperature and associated conduction mechanisms are discussed in both states.

  1. Slow recovery from severe inorganic arsenic poisoning despite treatment with DMSA (2.3-dimercaptosuccinic acid).

    Science.gov (United States)

    Stenehjem, Aud-E; Vahter, Marie; Nermell, Barbro; Aasen, Jorulf; Lierhagen, Syverin; Mørland, Jørg; Jacobsen, Dag

    2007-05-01

    A 39-year-old woman was hospitalized for nausea, diarrhea, vomiting, and weakness of unknown etiology. Her condition progressively deteriorated and she developed multiple organ failure and tetraplegia. The diagnosis of inorganic arsenic poisoning was established by measurements of arsenic in urine and serum, showing 2,000 microg/L (normal treatment probably had no significant effect on the total body clearance in our patient. The source of the poisoning was never detected, nor the motivation behind it. Criminal intent was suspected, but no verdict was given.

  2. Effect of ammonium sulfate, ammonium chloride and root-zone acidity on inorganic ion content of tobacco

    Science.gov (United States)

    Vessey, J. K.; Raper, C. D. Jr; Henry, L. T.; Raper CD, J. r. (Principal Investigator)

    1990-01-01

    Tobacco plants (Nicotiana tabacum L. cv NC82) were supplied with (NH4)2SO4 or NH4Cl at root-zone pH of 6.0 and 4.5 in hydroponic culture for 28 days. Dry matter accumulation, total N and C content, and leaf area and number were not affected by the NH4+ source or root-zone pH. Plants supplied with NH4Cl accumulated up to 1.2 mM Cl g DW-1, but accumulated 37% less inorganic H2PO4- and 47% less SO4(2-) than plants supplied with (NH4)2SO4. The large Cl- accumulation resulted in NH4Cl- supplied plants having a 31% higher inorganic anion (NO3-, H2, PO4-, SO4(2-), and Cl-) charge. This higher inorganic anion charge in the NH4Cl-supplied plants was balanced by a similar increase in K+ charge. Plants supplied with NH4Cl accumulated greater concentrations of Cl- in leaves (up to 5.1% of DW) than plants supplied with (NH4)2SO4 (less than -% DW). Despite the high Cl- concentration of leaves in NH4Cl supplied plants, these plants showed no symptoms of Cl- toxicity. This demonstrates that toxicity symptoms are not due solely to an interaction between high Cl- concentration in tissue and NH4+ nutrition. The increase in root-zone acidity to pH 4.5 from 6.0 did not induce toxicity symptoms.

  3. Screening of soybean germplasm for high inorganic phosphorus and low phytic acid

    Directory of Open Access Journals (Sweden)

    S. Abirami, A. Kalamani and T. Kalaimagal

    2014-09-01

    Full Text Available Phytic acid, is the major storage form of phosphorus in soybean [Glycine max (L. Merr.] which comprises 75% of total seed phosphorus. It decreases the availability of some essential elements via bonding between the negatively charged phytic acid and the positively charged elements. Thus, diets high in phytate may lead to nutrient deficiencies. So, identification of lines with low phytic acid is of paramount importance. A germplasm survey was conducted among 250 soybean accessions to identify the accessions with low phytic acid. Phytic acid content ranged between 0.84 and 7.07 mg/ g of soy flour. The genotypes with low phytic acid content viz., Williams, Williams 82, CNS – AVRDC line, RKS 52 and NRC 66 may be useful in breeding programs for the development of low phytic acid genotypes with improved nutritional value to overcome nutritional deficiency syndromes and meet the demand of biofortification.

  4. Measurement of inorganic arsenic species in rice after nitric acid extraction by HPLC-ICPMS: verification using XANES.

    Science.gov (United States)

    Maher, W; Foster, S; Krikowa, F; Donner, E; Lombi, E

    2013-06-04

    The measurement of As species in rice is normally accomplished by extraction followed by HPLC-ICPMS analysis. This method, however, has not been comprehensively validated by comparing these speciation results with XANES, which does not require sample extraction, due to the challenge of conducting XANES analysis at very low As concentrations. In this study As speciation data using nitric acid extraction/HPLC-ICPMS and XANES are compared to verify the efficacy of using 2% v/v nitric acid extraction and HPLC-ICPMS to measure inorganic As, DMA, and MA in reference rice materials and common rice varieties obtainable in Australia. Total As and As species (As(III), As(V), DMA, and MA) concentrations measured in 8 reference materials were in agreement with published values. XANES analysis was performed on 5 samples having total As concentrations ranging from 0.198 to 0.335 μg g(-1). XANES results gave similar proportions of total As(III), As(V), and DMA to HPLC-ICPMS. XANES was able to distinguish two forms of As(III): As(III) and As(III)GSH. Total As concentrations in rice samples varied from 0.006 to 0.45 μg g(-1) As (n = 47) with a mean ± std of 0.127 ± 0.112 μg g(-1) As with most As present as inorganic species (63 ± 26%). DMA was found in nearly all the rice samples with the majority of samples containing concentrations below 0.05 μg g(-1) As while MA concentrations were negligible (<0.003 μg g(-1) As). Six rice varieties produced in Australia, China, and Spain all had elevated DMA concentrations (0.170-0.399 μg g(-1) As) that were correlated with total As concentrations (r(2) = 0.7518). In conclusion, comparison of As speciation by HPLC-ICPMS and XANES showed that similar As species were detected indicating the appropriateness of using 2% v/v nitric acid for extraction of rice prior to speciation. Common rice varieties obtainable in Australia generally have low As concentrations with most As present as inorganic As.

  5. Indirect UV detection-ion-exclusion/cation-exchange chromatography of common inorganic ions with sulfosalicylic acid eluent.

    Science.gov (United States)

    Kozaki, Daisuke; Mori, Masanobu; Nakatani, Nobutake; Arai, Kaori; Masuno, Tomoe; Koseki, Masakazu; Itabashi, Hideyuki; Tanaka, Kazuhiko

    2013-01-01

    Herein, we describe indirect UV detection-ion-exclusion/cation-exchange chromatography (IEC/CEC) on a weakly acidic cation-exchange resin in the H(+)-form (TSKgel Super IC-A/C) using sulfosalicylic acid as the eluent. The goal of the study was to characterize the peaks detected by UV detector. The peak directions of analyte ions in UV at 315 nm were negative because the molar absorbance coefficients of analyte anions and cations were lower than that of the sulfosalicylic acid eluent. Good chromatographic resolution and high signal-to-noise ratios of analyte ions were obtained for the separations performed using 1.1 mM sulfosalicylic acid and 1.5 mM 18-crown-6 as the eluent. The relative standard deviations (RSDs) of the peak areas ranged from 0.6 to 4.9%. Lower detection limits of the analytes were achieved using indirect UV detection at 315 nm (0.23 - 0.98 μM) than those obtained with conductometric detection (CD) (0.61 - 2.1 μM) under the optimized elution conditions. The calibration curves were linear in the range from 0.01 to 1.0 mM except for Cl(-), which was from 0.02 to 2.0 mM. The present method was successfully applied to determine common inorganic ions in a pond water sample.

  6. Bioavailability of magnesium from inorganic and organic compounds is similar in rats fed a high phytic acid diet.

    Science.gov (United States)

    Bertinato, Jesse; Plouffe, Louise J; Lavergne, Christopher; Ly, Catherine

    2014-01-01

    A large section of the North American population is not meeting recommended intakes for magnesium (Mg). Supplementation and consumption of Mg-fortified foods are ways to increase intake. Currently, information on Mg bioavailability from different compounds and their efficacy in improving Mg status is scant. This study compared the relative ability of inorganic and organic Mg compounds to preserve the Mg status of rats when fed at amounts insufficient to retain optimal Mg status. Male Sprague-Dawley rats (n=12/diet group) were fed one of eight test diets supplemented with phytic acid (5 g/kg diet) and low levels of Mg (155 mg elemental Mg/kg diet) from Mg oxide, Mg sulphate, Mg chloride, Mg citrate, Mg gluconate, Mg orotate, Mg malate or ethylenediaminetetraacetic acid disodium Mg salt for five weeks. Rats were also fed three control diets that did not contain added phytic acid but were supplemented with 500 (NMgO, normal), 155 (LMgO, low) or 80 (DMgO, deficient) mg of Mg per kg diet as Mg oxide. Mg concentrations in femur, serum and urine showed a graded decrease in rats fed the control diets with lower Mg. Mg concentrations did not differ (P≥0.05) between rats fed the different test diets. Addition of phytic acid to the diet did not affect the Mg status of the rats. The results indicate that any differences in the Mg bioavailability of the compounds were small and physiologically irrelevant.

  7. Screening of soybean germplasm for high inorganic phosphorus and low phytic acid

    OpenAIRE

    S. Abirami, A. Kalamani and T. Kalaimagal

    2014-01-01

    Phytic acid, is the major storage form of phosphorus in soybean [Glycine max (L.) Merr.] which comprises 75% of total seed phosphorus. It decreases the availability of some essential elements via bonding between the negatively charged phytic acid and the positively charged elements. Thus, diets high in phytate may lead to nutrient deficiencies. So, identification of lines with low phytic acid is of paramount importance. A germplasm survey was conducted among 250 soybean accessions to identify...

  8. Crystal structure of caesium hydrogen (L)-aspartate and an overview of crystalline compounds of aspartic acid with inorganic constituents

    Energy Technology Data Exchange (ETDEWEB)

    Fleck, M. [Universitaet Wien (Austria). Institut fuer Mineralogie und Kristallographie; Emmerich, R.; Bohaty, L. [Universitaet zu Koeln (Austria). Institut fuer Kristallographie

    2010-08-15

    The crystal structure of the new polar compound caesium hydrogen (L)-aspartate, Cs(C{sub 4}H{sub 6}NO{sub 4}), (abbreviated: Cs(L -AspH)) was determined from single crystal X-ray diffraction data; it comprises two crystallographically different L -AspH anions that are connected via caesium cations to form a three dimensional framework. The Cs ions are irregularly sevenfold[Cs1O{sub 7}] respectively eightfold[Cs2O{sub 8}] coordinated to all {alpha}- and {beta}- carboxylate oxygen atoms. Cs(L -AspH) represents a novel structure type of its own, as do most compounds of (L)-aspartic acid with inorganic constituents. A brief summary of such structurally known aspartates is given. (copyright 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  9. Correlations between the contents of phytic acid and inorganic phosphorous and downy mildew resistance of corn inbred lines

    Directory of Open Access Journals (Sweden)

    Pantipa Na Chiangmai

    2015-10-01

    Full Text Available Seeds of corn inbred lines collected at the National Corn and Sorghum Research Center (NCSRC, Kasetsart University, were analyzed to determine the contents of phytic acid (PA and inorganic phosphorous (InP. These 28 and 29 inbred lines were cultivated at the NCSRC (in the 2008 late rainy season and 2009 early rainy season to evaluate their resistance to corn downy mildew caused by Peronosclerospora sorghi. Results showed that the values of the PA, InP contents and downy mildew infection were statistically different among these inbred lines in both seasons. However, there were no correlations between the contents of either PA or InP and downy mildew infection.

  10. Ampholine-functionalized hybrid organic-inorganic silica material as sorbent for solid-phase extraction of acidic and basic compounds.

    Science.gov (United States)

    Wang, Tingting; Chen, Yihui; Ma, Junfeng; Chen, Mingliang; Nie, Chenggang; Hu, Minjie; Li, Ying; Jia, Zhijian; Fang, Jianghua; Gao, Haoqi

    2013-09-20

    A novel sorbent for solid-phase extraction (SPE) was synthesized by chemical immobilization of ampholine on hybrid organic-inorganic silica material. The ampholine-functionalized hybrid organic-inorganic silica sorbent is consisted of aliphatic amine groups, carboxyl groups and long carbon chains, allowing for extraction of both acidic and basic compounds. The retention properties of the developed sorbent were evaluated for 1-hydroxy-2-naphthoic acid (HNA), 1-naphthoic acid (NA), 3-hydroxybenzoic acid (HBA), benzoic acid (BA), sorbic acid (SA), vanillic aldehyde (VA), butyl 4-hydroxybenzoate (BHB), propyl 4-hydroxybenzoate (PHB), ethyl 4-hydroxybenzoate (EHB), and methyl 4-hydroxybenzoate (MHB). The results show that such a sorbent has three types of interaction, i.e., electrostatic interaction, hydrophobic interaction, and hydrogen bonding, exhibiting high extraction efficiency towards the compounds tested. The adsorption capacities of the analytes ranged from 0.61 to 6.54μgmg(-1). The reproducibility of the sorbent preparation was evaluated at three spiking concentration levels, with relative standard deviations (RSDs) of 1.0-10.5%. The recoveries of ten acidic and basic compounds spiked in beverage Coca-Cola(®) sample ranged from 82.5% to 98.2% with RSDs less than 5.8%. Under optimum conditions, the ampholine-functionalized hybrid organic-inorganic silica sorbent rendered higher extraction efficiency for acidic compounds than that of the commercially available ampholine-functionalized silica particles, and was comparable to that of the commercial Oasis WAX and Oasis WCX.

  11. The synthesis of amino acids and sugars on an inorganic template from constituents of the prebiotic atmosphere

    Science.gov (United States)

    Field, B. O.; Spencer, J. E. D.

    1990-05-01

    Inelastic Electron Tunnelling Spectroscopy (IETS) has been used to identify the reaction products present on an alumina surface when it is exposed to likely components of the earth's prebiotic atmosphere. The alumina barrier of Al-AlO x -Pb tunnelling junctions have been exposed to water; aqueous ammonia; wet carbon monoxide gas and to aqueous formaldehyde vapour under normal atmospheric conditions at room temperature. The water spectrum shows strong coincidence with that of a genuine sample of formic acid. It is proposed that atmospheric CO2 is involved in this surface catalyzed reaction. The aqueous ammonia spectrum is assigned as an amino acid species produced from ammonia, water and atmospheric carbon dioxide. This spectrum compares very closely with the tunnelling spectrum of a genuine sample of glycine. The wet carbon monoxide spectrum and the aqueous formaldehyde spectrum have been produced by an infusion doping process. These spectra of CO and aqueous formaldehyde are assigned as a sugar like polymer or a sugar formed on the alumina surface. A tunnelling spectrum of D(-) fructose has been produced to aid this assignment. The role of an inorganic template such as alumina in the original prebiotic synthesis of amino acids and sugars is considered.

  12. Effect of organic/inorganic compounds on the enzymes in soil under acid rain stress

    Institute of Scientific and Technical Information of China (English)

    LIU Guang-shen; XU Dong-mei; WANG Li-ming; LI Ke-bin; LIU Wei-ping

    2004-01-01

    The main effects of pollutions including acid rain, Cu2+, atrazine and their combined products on theactivities of urease, invertin, acid phosphatase and catalase were studied by means of orthogonal test. The resultsshowed that H + and Cu2+ had significant influence on the activities of four enzymes and the ability of their inhibitingfollowed the order: H+ > Cu2+ . Al3+ and atrazine only had litter effects on the activity of urease and phosphatase,respectively. Furthermore, interaction analysis revealed that Cu2+ -H+ affected on the activity of acid phosphatasesignificantly and antagonism on invertin and urease, Cu2+ -atrazine only exhibited the synergism on the activity ofacid phosphatase. But atrazine-H+ had non-interaction within the investigated concentration range. Among fourenzymes, acid phosphatase was the most sensitive one to the contaminations.

  13. Glutamic acid-149 is important for enzymatic activity of yeast inorganic pyrophosphatase.

    Science.gov (United States)

    Gonzalez, M A; Cooperman, B S

    1986-11-04

    Modification of Saccharomyces cerevisiae inorganic pyrophosphatase (PPase) with 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide is known to lead to a loss of enzymatic activity, the rate of which is decreased in the presence of ligands binding to the active site [Cooperman, B. S., & Chiu, N. Y. (1973) Biochemistry 12, 1676-1682; Heitman, P., & Uhlig, H. J. (1974) Acta Biol. Med. Ger. 32, 565-594]. In this work we show that, when such inactivation is carried out in the presence of [14C]glycine ethyl ester (GEE), GEE is covalently incorporated into PPase, incorporation into the most highly labeled tryptic peptide is site-specific, as evidenced by the reduction of such incorporation in the presence of the active site ligands Zn2+ and Pi, the extent of formation of this specifically labeled peptide correlates with the fractional loss of PPase activity, and the specifically labeled peptide corresponds to residues 145-153 and the position of incorporation within this peptide is Glu-149. The significance of our findings for the location of the active site and for the catalytic mechanism of PPase is briefly considered in the light of the 3-A X-ray crystallographic structure of Arutyunyun and his colleagues [Arutyunyun, E. G., et al. (1981) Dokl. Akad. Nauk SSSR 258, 1481-1485; Kuranova, I. P., et al. (1983) Bioorg. Khim. 9, 1611-1919; Terzyan, S. S., et al. (1984) Bioorg. Khim. 10, 1469-1482].

  14. Study of Inorganic Pollutants Removal from Acid Mine Drainage by Hemp Hurds

    Science.gov (United States)

    Demcak, Stefan; Balintova, Magdalena

    2016-12-01

    Sulphates in wastewaters have an origin as the by-products of a variety of industrial operations. A specific and major producer of such effluents, which contained sulphates and heavy metals, is the mining industry. These contaminants should be removed from wastewater using an adequate process of treatment. The paper deals with selected heavy metals (iron, cooper, and manganese) and sulphate removal from acid mine drainage outflowing from an abandoned mine in Smolnik (Slovakia) using the modified biosorbent - Holland hemp hurds. Pre-treatment of acid mine drainage was based on oxidation of ferrous cations from acid mine drainage by hydrogen peroxide and subsequent precipitation. The precipitate were analysed by infrared spectrometry which found the precipitate containing hydroxide and sulphate functional groups. During this process the concentration of sulphate decreased by 43.8 %. Hemp hurds modified by NaOH decreased concentration of Cu2+ in solution by about 70 %

  15. Separation and immobilization of Sr and Cs contained in acidic media by using inorganic ion-exchangers. Literature survey

    Energy Technology Data Exchange (ETDEWEB)

    Yamagishi, Isao [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    2001-07-01

    The present study deals with the survey of inorganic ion-exchangers suitable for separation and immobilization of Sr and Cs contained in acidic high-level liquid waste. The stabilities of published waste forms and their preparation processes were evaluated from the standpoint of conversion of exchangers containing Sr and Cs into appropriate waste forms. The essential results are below. (1) For separation and immobilization of Cs, crystalline silicotitanate seems to be the most promising exchanger. Insoluble ferrocyanides and phosphates are not suitable for immobilization without additives. Mordenite is inexpensive and commercially available but it would dissolve in highly acidic media. (2) For selective separation of Sr, there is no promising exchanger up to now. It is necessary either to modify separation condition or to synthesize a novel exchanger. (3) Soluble salts, glasses and ceramics are proposed as a storage or disposal form of separated Sr and Cs. Ceramics sintered by hot-pressing are favorable waste forms of inorganic ion-exchangers but their leachabilities and thermal conductivities are largely influenced by qualities of products. Crystallinity of a sintered exchanger depends on its composition. Exchanges of low Cs contents are often converted into amorphous materials whose chemical stabilities depend on solubilities of components of exchangers. (4) A new exchanger to be synthesized is crystalline and selective toward Sr and Cs. One meq/g is enough for Sr and Cs capacities, which are restricted by thermal and transmutation effects. Composition of the exchanger should be selected from the point of a scenario of separation and disposal. The solubilities of SiO{sub 2}, TiO{sub 2}, ZrO{sub 2}, Nb{sub 2}O{sub 5} and Ta{sub 2}O{sub 5} are low in acidic media and those of Al{sub 2}O{sub 3}, TiO{sub 2} and ZrO{sub 2}, in disposal circumstances. (5) Future works are optimization of separation scheme including development of exchangers, simplification of

  16. Inorganic polymers from laterite using activation with phosphoric acid and alkaline sodium silicate solution: Mechanical and microstructural properties

    Energy Technology Data Exchange (ETDEWEB)

    Lassinantti Gualtieri, Magdalena, E-mail: magdalena.gualtieri@unimore.it [Dipartimento di Ingegneria " Enzo Ferrari" , Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy); Romagnoli, Marcello [Dipartimento di Ingegneria " Enzo Ferrari" , Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy); Pollastri, Simone; Gualtieri, Alessandro F. [Dipartimento di Scienze Chimiche e Geologiche, Università degli studi di Modena e Reggio Emilia, Via S. Eufemia 19I, I-41121 Modena (Italy)

    2015-01-15

    Geopolymers from laterite, an iron-rich soil available in developing countries, have great potential as building materials. In this work, laterite from Togo (Africa) was used to prepare geopolymers using both phosphoric acid and alkaline sodium silicate solution. Microstructural properties were investigated by scanning electron microscopy, X-ray powder diffraction and mercury porosimetry, whereas thermal properties were evaluated by thermal analyses. The local environment of iron was studied by X-ray Absorption Spectroscopy (XANES region). The mechanical properties were determined. Modulus of Rupture and Young's modulus fell in the ranges 3.3–4.5 MPa and 12–33 GPa, respectively, rendering the materials good candidates for construction purposes. Heating above 900 °C results in weight-gain, presumably due to iron redox reactions. X-ray Absorption Spectroscopy data evidence changes in the chemical and structural environments of iron following thermal treatment of geopolymers. These changes indicate interaction between the geopolymer structure and iron during heating, possibly leading to redox properties. -- Highlights: •Geopolymerization of laterite is promising for fabrication of building materials. •Both phosphoric acid and alkaline sodium silicate solution can be used for activation. •Thermally activated redox properties of the inorganic polymers were observed.

  17. Phytic acid and inorganic phosphate composition in soybean lines with independent IPK1 mutations

    Science.gov (United States)

    Soybean [Glycine max (L.) Merr] seeds contain a large amount of phosphorus (P), which is stored as phytic acid (PA). PA is indigestible by nonruminent livestock and considered an anti-nutritional factor because PA chelates divalent cations and prevents the uptake of essential nutrients. Interest in...

  18. Size-controlled synthesis and formation mechanism of manganese oxide OMS-2 nanowires under reflux conditions with KMnO4 and inorganic acids

    Science.gov (United States)

    Zhang, Qin; Cheng, Xiaodi; Qiu, Guohong; Liu, Fan; Feng, Xionghan

    2016-05-01

    This study presents a simplified approach for size-controlled synthesis of manganese oxide octahedral molecular sieve (OMS-2) nanowires using potassium permanganate (KMnO4) and different inorganic acids (HCl, HNO3, and H2SO4) under reflux conditions. The morphology and nanostructure of the synthesized products are characterized by X-ray diffraction, Ar adsorption, and electron microscopy analysis, in order to elucidate the controlling effects of acid concentration and type as well as the formation mechanism of OMS-2 nanowires. The concentration of inorganic acid is a crucial factor controlling the phase of the synthesized products. OMS-2 nanowires are obtained with HCl at the concentration ≥0.96 mol/L or with HNO3 and H2SO4 at the concentrations ≥0.72 mol/L. Differently, the type of inorganic acid effectively determines the particle size of OMS-2 nanowires. When the acid is changed from HCl to HNO3 and H2SO4 in the reflux system, the average length of OMS-2 declines significantly by 60-70% (1104-442 and 339 nm), with minor decreased in the average width (43-39 and 34 nm). The formation of OMS-2 nanowires under reflux conditions with KMnO4 and inorganic acids involves a two-step process, i.e., the initial formation of layered manganese oxides, and subsequent transformation to OMS-2 via a dissolution-recrystallization process under acidic conditions. The proposed reflux route provides an alternative approach for synthesizing OMS-2 nanowires as well as other porous nano-crystalline OMS materials.

  19. Sea salt aerosols as a reactive surface for inorganic and organic acidic gases in the arctic troposphere

    Directory of Open Access Journals (Sweden)

    J. W. Chi

    2015-06-01

    Full Text Available Sea salt aerosols (SSA are dominant particles in the arctic atmosphere and determine the polar radiative balance. SSA react with acidic pollutants that lead to changes of physical and chemical properties of their surface, which in turn alter their hygroscopic and optical properties. Transmission electron microscopy with energy-dispersive X-ray spectrometry was used to analyze morphology, composition, size, and mixing state of individual SSA at Ny-Ålesund, Svalbard in summertime. Individual fresh SSA contained cubic NaCl coated by certain amounts of MgCl2 and CaSO4. Individual partially aged SSA contained irregular NaCl coated by a mixture of NaNO3, Na2SO4, Mg(NO32, and MgSO4. The comparison suggests the hydrophilic MgCl2 coating in fresh SSA likely intrigued the heterogeneous reactions at the beginning of SSA and acidic gases. Individual fully aged SSA normally had Na2SO4 cores and an amorphous coating of NaNO3. Elemental mappings of individual SSA particles revealed that as the particles ageing Cl gradually decreased but the C, N, O, and S content increased. 12C14N− mapping from nanoscale secondary ion mass spectrometry indicates that organic matter increased in the aged SSA compared with the fresh SSA. 12C14N− line scans further show that organic matter was mainly concentrated on the aged SSA surface. These new findings indicate that this mixture of organic matter and NaNO3 on particle surfaces determines their hygroscopic and optical properties. These abundant SSA, whose reactive surfaces absorb inorganic and organic acidic gases in the arctic troposphere, need to be incorporated into atmospheric chemical models.

  20. A lipidomic approach to understanding free fatty acid lipogenesis derived from dissolved inorganic carbon within cnidarian-dinoflagellate symbiosis.

    Directory of Open Access Journals (Sweden)

    Simon R Dunn

    Full Text Available The cnidarian-dinoflagellate symbiosis is arguably one of the most important within the marine environment in that it is integral to the formation of coral reefs. However, the regulatory processes that perpetuate this symbiosis remain unresolved. It is essential to understand these processes, if we are to elucidate the mechanisms that support growth and resource accumulation by coral host, and conversely, recently observed reduction and/or mortality of corals in response to rapid environmental change. This study specifically focused on one area of metabolic activity within the symbiosis, that of free fatty acid synthesis within both the dinoflagellate symbionts and cnidarian host. The main model system used was Aiptasia pulchella and Symbiodinium sp. in combination with aposymbiotic A. pulchella, the symbiotic coral Acropora millepora system and dinoflagellate culture. Fatty acids (FAs were selected because of their multiple essential roles inclusive of energy storage (resource accumulation, membrane structure fluidity and cell signaling. The study addressed free FA lipogenesis by using a new method of enriched stable isotopic ((13C incorporation from dissolved inorganic carbon (DI(13C combined with HPLC-MS. FAs derived from DI(13C aligned with a mixture of known lipogenesis pathways with the addition of some unusual FAs. After 120 hr, (13C-enriched FA synthesis rates were attributed to only a complex integration of both n-3 and n-6 lipogenesis pathways within the dinoflagellate symbionts. Furthermore, there was no detectible evidence of symbiont derived enriched isotope fatty acids, catabolized (13C derivatives or DI(13C being directly utilized, in host late n-6 pathway long-chain FA lipogenesis. These findings do not align with a popular mutualistic translocation model with respect to the use of translocated symbiont photoassimilates in host long-chain FA lipogenesis, which has important connotations for linking nutrient sources with

  1. Transition metal modified and partially calcined inorganic-organic pillared clays for the adsorption of salicylic acid, clofibric acid, carbamazepine, and caffeine from water.

    Science.gov (United States)

    Cabrera-Lafaurie, Wilman A; Román, Félix R; Hernández-Maldonado, Arturo J

    2012-11-15

    Pharmaceutical and Personal Care Products (PPCPs) are considered emerging contaminants, and their efficient removal from water is going to be a challenging endeavor. Microporous adsorbent materials, including pillared clays, could offer a potential solution if tailored properly. Although pillared clays have been employed previously for the removal of organics, the effective removal of PPCPs will only be possible if their surface and textural properties are manipulated from the bottom-up. This work presents the use of modified inorganic-organic pillared clays (IOCs) for the adsorption of salicylic acid, clofibric acid, carbamazepine, and caffeine. The IOCs have been modified with Co(2+), Cu(2+), or Ni(2+) to induce complexation-like adsorbate-adsorbent interactions at ambient conditions, in an attempt to provide an efficient and yet reversible driving force in the sub-ppm concentration range. Furthermore, the IOCs were partially calcined to increase effective surface area by an order of magnitude while preserving some hydrophobicity. In general, the Ni(2+) IOCs exhibited the greatest interaction with salicylic and clofibric acids, respectively, while the Co(2+) adsorbents excelled at adsorbing caffeine at low concentrations. All of the metal-modified IOCs showed comparable adsorption capacities for the case of carbamazepine, probably due to the lack of availability of particular functional groups in this adsorbate.

  2. Sialic acid mediates the initial binding of positively charged inorganic particles to alveolar macrophage membranes.

    Science.gov (United States)

    Gallagher, J E; George, G; Brody, A R

    1987-06-01

    Pulmonary macrophages phagocytize inhaled particles and are postulated to play a role in the development of pulmonary interstitial fibrogenesis. The basic biologic mechanisms through which inhaled particles bind to macrophage membranes and subsequently are phagocytized remain unclear. We hypothesize that positively charged particles bind to negatively charged sialic acid (SA) residues on macrophage membranes. Alveolar Macrophages (AM) were collected by saline lavage from normal rat lungs. The cells adhered to plastic coverslips in serum-free phosphate buffered saline at 37 degrees C for 45 min and then were maintained at 4 degrees C for the binding experiments. Even distribution of SA groups on AM surfaces was demonstrated by scanning electron microscopy of wheat germ agglutinin (WGA) conjugated to 50 nm gold spheres. The WGA is a lectin that binds specifically to sialic acid, and pretreatment of AM with this lectin prevented the binding of positively charged carbonyl iron (C-Fe) spheres, aluminum (Al) spheres, and chrysotile asbestos fibers to AM surfaces. Limulus protein, another lectin with binding specificity for SA, similarly blocked the binding of positively charged spheres and chrysotile asbestos fibers but not negatively charged glass spheres or crocidolite asbestos fibers. Con A and ricin, lectins that bind to mannose and galactose residues, respectively, did not block particle binding. When both positively charged iron spheres and negatively charged glass spheres were prebound to AM membranes, subsequent treatment with WGA displaced only the positively charged spheres from macrophage surfaces. Con A and ricin had no effect on prebound positively charged C-Fe and Al spheres.(ABSTRACT TRUNCATED AT 250 WORDS)

  3. Monomethylarsonous acid, but not inorganic arsenic, is a mitochondria-specific toxicant in vascular smooth muscle cells.

    Science.gov (United States)

    Pace, Clare; Banerjee, Tania Das; Welch, Barrett; Khalili, Roxana; Dagda, Ruben K; Angermann, Jeff

    2016-09-01

    Arsenic exposure has been implicated as a risk factor for cardiovascular diseases, metabolic disorders, and cancer, yet the role mitochondrial dysfunction plays in the cellular mechanisms of pathology is largely unknown. To investigate arsenic-induced mitochondrial dysfunction in vascular smooth muscle cells (VSMCs), we exposed rat aortic smooth muscle cells (A7r5) to inorganic arsenic (iAs(III)) and its metabolite monomethylarsonous acid (MMA(III)) and compared their effects on mitochondrial function and oxidative stress. Our results indicate that MMA(III) is significantly more toxic to mitochondria than iAs(III). Exposure of VSMCs to MMA(III), but not iAs(III), significantly decreased basal and maximal oxygen consumption rates and concomitantly increased compensatory extracellular acidification rates, a proxy for glycolysis. Treatment with MMA(III) significantly increased hydrogen peroxide and superoxide levels compared to iAs(III). Exposure to MMA(III) resulted in significant decreases in mitochondrial ATP, aberrant perinuclear clustering of mitochondria, and decreased mitochondrial content. Mechanistically, we observed that mitochondrial superoxide and hydrogen peroxide contribute to mitochondrial toxicity, as treatment of cells with MnTBAP (a mitochondrial superoxide dismutase mimetic) and catalase significantly reduced mitochondrial respiration deficits and cell death induced by both arsenic compounds. Overall, our data demonstrates that MMA(III) is a mitochondria-specific toxicant that elevates mitochondrial and non-mitochondrial sources of ROS.

  4. A magnetic organic inorganic composite: Synthesis and characterization of magnetic 5-aminosalicylic acid intercalated layered double hydroxides

    Science.gov (United States)

    Zhang, Hui; Zou, Kang; Sun, Hui; Duan, Xue

    2005-11-01

    A core-shell structured magnetic layered organic-inorganic material involving 5-aminosalicylic acid (5-ASA) intercalated Zn-Al layered double hydroxides (LDHs) and magnesium ferrite (MgFe 2O 4) is assembled by a coprecipitation method. The powder X-ray diffraction results show the coexistence of the clear but weak diffractions of MgFe 2O 4 and ordered relatively stronger reflections of 5-ASA intercalated LDHs. The TEM image of magnetic 5-ASA intercalated LDHs reveals that the LDHs layer covers the MgFe 2O 4 particles or their aggregates with particle size of 50-80 nm. The vibration sample magnetization (VSM) measurements exhibit the increase in saturation magnetization of magnetic 5-ASA intercalated LDHs samples with increasing amount of magnetic core. The XPS analyses account for a majority of Zn, Al and O atoms on the surface of magnetic particles. It is suggested that the magnetic core MgFe 2O 4 was coated with LDHs layer probably through Zn-O-Mg and Al-O-Mg linkages, and a core-shell structured model is tentatively proposed.

  5. Effects of crystalline structures and surface functional groups on the adsorption of haloacetic acids by inorganic materials.

    Science.gov (United States)

    Punyapalakul, Patiparn; Soonglerdsongpha, Suwat; Kanlayaprasit, Chutima; Ngamcharussrivichai, Chawalit; Khaodhiar, Sutha

    2009-11-15

    The effects of the crystalline structure and surface functional groups of porous inorganic materials on the adsorption of dichloroacetic acid (DCAA) were evaluated by using hexagonal mesoporous silicates (HMS), two surface functional group (3-aminopropyltriethoxy- and 3-mercaptopropyl-) modified HMSs, faujasite Y zeolite and activated alumina as adsorbents, and compared with powdered activated carbon (PAC). Selective adsorption of HAA(5) group was studied by comparing single and multiple-solute solution, including effect of common electrolytes in tap water. Adsorption capacities were significantly affected by the crystalline structure. Hydrogen bonding is suggested to be the most important attractive force. Decreasing the pH lower than the pH(zpc) increased the DCAA adsorption capacities of these adsorbents due to electrostatic interaction and hydrogen bonding caused by protonation of the hydronium ion. Adsorption capacities of HAA(5) on HMS did not relate to molecular structure of HAA(5). Common electrolytes did not affect the adsorption capacities and selectivity of HMS for HAA5, while they affected those of PAC.

  6. Lophira中无机元素及氨基酸含量测定%Study on the contents of amino acids and inorganic elements in Lophira

    Institute of Scientific and Technical Information of China (English)

    陈晓岚; 卢建莎; 郭蕾; 龙跃; 赵清治; 刘聚胜; 魏莉莉

    2001-01-01

    To determine the contents of some inorganic elements and aminoacid in a natural plant-Lophira.Method: The contents of inorganic elements were determined by ICP and amino acids, by amino analyzer, respectively. Resultsand conclusion: The contents such as manganese, strontia and zino in this natural plant were high. Eighteen amino acids including seven human essential amino acids were detected. The high contents of some inorganic elements and hmnan essential elementsamino acids in Lophira perhaps could explain its folk diagnostic applications to a certain degree.%目的:测定天然植物Lophira中无机元素和氨基酸的含量。方法:用等离子体原子光谱,测定Lophira酸溶液中几种重要无机元素含量;用氨基酸自动分析仪测定氨基酸的含量。结果与结论:天然植物Lophira中具有较高的锌、锶和锰;含18种氨基酸,7种为必需氨基酸,氨基酸总含量为20.17mg/g。

  7. Use of stirred tanks for studying matrix effects caused by inorganic acids, easily ionized elements and organic solvents in inductively coupled plasma atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Paredes, Eduardo [Departamento de Quimica Analitica, Nutricion y Bromatologia, University of Alicante, 03080 Alicante (Spain); Maestre, Salvador E. [Departamento de Quimica Analitica, Nutricion y Bromatologia, University of Alicante, 03080 Alicante (Spain); Todoli, Jose L. [Departamento de Quimica Analitica, Nutricion y Bromatologia, University of Alicante, 03080 Alicante (Spain)]. E-mail: jose.todoli@ua.es

    2006-03-15

    A stirred tank was used for the first time to elucidate the mechanism responsible for inductively coupled plasma atomic emission spectroscopy (ICP-AES) matrix effects caused by inorganic, acids and easily ionized elements (EIEs), as well as organic, ethanol and acetic acid, compounds. In order to gradually increase the matrix concentration, a matrix solution was introduced inside a stirred container (tank) initially filled with an aqueous multielement standard. PolyTetraFluoroEthylene (PTFE) tubing was used to deliver the resulting solution to the liquid sample introduction system. Matrix concentration ranged from 0 to 2 mol l{sup -1} in the case of inorganic acids (i.e., nitric, sulfuric, hydrochloric and a mixture of them), from 0 to about 2500 mg l{sup -1} for EIEs (i.e., sodium, calcium and mixtures of both) and from 0% to 15%, w/w for organic compounds. Up to 40-50 different solutions were prepared and measured in a period of time shorter than 6-7 min. This investigation was carried out in terms of emission intensity and tertiary aerosols characteristics. The experimental setup used in the present work allowed to thoroughly study the effect of matrix concentration on analytical signal. Generally speaking, the experiments concerning tertiary aerosol characterization revealed that, in the case of inorganic acids and EIEs, the mechanism responsible for changes in aerosol characteristics was the droplet fission. In contrast, for organic matrices it was found that the interference was caused by a change in both aerosol transport and plasma thermal characteristics. The extent of the interferences caused by organic as well as inorganic compounds was compared for a set of 14 emission lines through a wide range of matrix concentrations. With a stirred tank, it is possible to choose an efficient internal standard for any given matrix composition. The time required to complete this procedure was shorter than 7 min.

  8. Effects of Organic and Inorganic Nitrogen on the Growth and Production of Domoic Acid by Pseudo-nitzschia multiseries and P. australis (Bacillariophyceae in Culture

    Directory of Open Access Journals (Sweden)

    Véronique Martin-Jézéquel

    2015-11-01

    Full Text Available Over the last century, human activities have altered the global nitrogen cycle, and anthropogenic inputs of both inorganic and organic nitrogen species have increased around the world, causing significant changes to the functioning of aquatic ecosystems. The increasing frequency of Pseudo-nitzschia spp. in estuarine and coastal waters reinforces the need to understand better the environmental control of its growth and domoic acid (DA production. Here, we document Pseudo-nitzschia spp. growth and toxicity on a large set of inorganic and organic nitrogen (nitrate, ammonium, urea, glutamate, glutamine, arginine and taurine. Our study focused on two species isolated from European coastal waters: P. multiseries CCL70 and P. australis PNC1. The nitrogen sources induced broad differences between the two species with respect to growth rate, biomass and cellular DA, but no specific variation could be attributed to any of the inorganic or organic nitrogen substrates. Enrichment with ammonium resulted in an enhanced growth rate and cell yield, whereas glutamate did not support the growth of P. multiseries. Arginine, glutamine and taurine enabled good growth of P. australis, but without toxin production. The highest DA content was produced when P. multiseries grew with urea and P. australis grew with glutamate. For both species, growth rate was not correlated with DA content but more toxin was produced when the nitrogen source could not sustain a high biomass. A significant negative correlation was found between cell biomass and DA content in P. australis. This study shows that Pseudo-nitzschia can readily utilize organic nitrogen in the form of amino acids, and confirms that both inorganic and organic nitrogen affect growth and DA production. Our results contribute to our understanding of the ecophysiology of Pseudo-nitzschia spp. and may help to predict toxic events in the natural environment.

  9. Effects of Organic and Inorganic Nitrogen on the Growth and Production of Domoic Acid by Pseudo-nitzschia multiseries and P. australis (Bacillariophyceae) in Culture

    Science.gov (United States)

    Martin-Jézéquel, Véronique; Calu, Guillaume; Candela, Leo; Amzil, Zouher; Jauffrais, Thierry; Séchet, Véronique; Weigel, Pierre

    2015-01-01

    Over the last century, human activities have altered the global nitrogen cycle, and anthropogenic inputs of both inorganic and organic nitrogen species have increased around the world, causing significant changes to the functioning of aquatic ecosystems. The increasing frequency of Pseudo-nitzschia spp. in estuarine and coastal waters reinforces the need to understand better the environmental control of its growth and domoic acid (DA) production. Here, we document Pseudo-nitzschia spp. growth and toxicity on a large set of inorganic and organic nitrogen (nitrate, ammonium, urea, glutamate, glutamine, arginine and taurine). Our study focused on two species isolated from European coastal waters: P. multiseries CCL70 and P. australis PNC1. The nitrogen sources induced broad differences between the two species with respect to growth rate, biomass and cellular DA, but no specific variation could be attributed to any of the inorganic or organic nitrogen substrates. Enrichment with ammonium resulted in an enhanced growth rate and cell yield, whereas glutamate did not support the growth of P. multiseries. Arginine, glutamine and taurine enabled good growth of P. australis, but without toxin production. The highest DA content was produced when P. multiseries grew with urea and P. australis grew with glutamate. For both species, growth rate was not correlated with DA content but more toxin was produced when the nitrogen source could not sustain a high biomass. A significant negative correlation was found between cell biomass and DA content in P. australis. This study shows that Pseudo-nitzschia can readily utilize organic nitrogen in the form of amino acids, and confirms that both inorganic and organic nitrogen affect growth and DA production. Our results contribute to our understanding of the ecophysiology of Pseudo-nitzschia spp. and may help to predict toxic events in the natural environment. PMID:26703627

  10. Polyaspartic acid facilitates oxolation within iron(iii) oxide pre-nucleation clusters and drives the formation of organic-inorganic composites

    Science.gov (United States)

    Scheck, J.; Drechsler, M.; Ma, X.; Stöckl, M. T.; Konsek, J.; Schwaderer, J. B.; Stadler, S. M.; De Yoreo, J. J.; Gebauer, D.

    2016-12-01

    The interplay between polymers and inorganic minerals during the formation of solids is crucial for biomineralization and bio-inspired materials, and advanced material properties can be achieved with organic-inorganic composites. By studying the reaction mechanisms, basic questions on organic-inorganic interactions and their role during material formation can be answered, enabling more target-oriented strategies in future synthetic approaches. Here, we present a comprehensive study on the hydrolysis of iron(iii) in the presence of polyaspartic acid. For the basic investigation of the formation mechanism, a titration assay was used, complemented by microscopic techniques. The polymer is shown to promote precipitation in partly hydrolyzed reaction solutions at the very early stages of the reaction by facilitating iron(iii) hydrolysis. In unhydrolyzed solutions, no significant interactions between the polymer and the inorganic solutes can be observed. We demonstrate that the hydrolysis promotion by the polymer can be understood by facilitating oxolation in olation iron(iii) pre-nucleation clusters. We propose that the adsorption of olation pre-nucleation clusters on the polymer chains and the resulting loss in dynamics and increased proximity of the reactants is the key to this effect. The resulting composite material obtained from the hydrolysis in the presence of the polymer was investigated with additional analytical techniques, namely, scanning and transmission electron microscopies, light microscopy, atomic force microscopy, zeta potential measurements, dynamic light scattering, and thermogravimetric analyses. It consists of elastic, polydisperse nanospheres, ca. 50-200 nm in diameter, and aggregates thereof, exhibiting a high polymer and water content.

  11. Chemical characterization of the inorganic fraction of aerosols and mechanisms of the neutralization of atmospheric acidity in Athens, Greece

    Directory of Open Access Journals (Sweden)

    E. T. Karageorgos

    2007-06-01

    + and Cl, while SO42−, Ca2+ and NH4+ were the major ionic components of the fine fraction. In the fine particles, a low molar ratio of NH4+/SO42− indicated an ammonium-poor ambient air, and together with inter-ionic correlations suggested that atmospheric ammonia is the major neutralizing agent of sulfate, while being insufficient to neutralize it to full extend. The formation of NH4NO3 is therefore not favored and additional contribution to the neutralization of acidity has been shown to be provided by Ca2+ and Mg2+. In the coarse particle fraction, the predominantly abundant Ca2+ has been found to correlate well with NO3 and SO42−, indicating its role as important neutralizing agent in this particle size range. The proximity of the location under study to the sea explains the important concentrations of salts with marine origin like NaCl and MgCl2 that were found in the coarse fraction, while chloride depletion in the gaseous phase was found to be limited to the fine particulate fraction. Total analyzed inorganic mass (elemental+ionic was found to be ranging between approximately 25–33% of the total coarse particle mass and 35–42% of the total fine particle mass.

  12. Fatty Acid Profiles of Supraspinatus, Longissimus lumborum and Semitendinosus Muscles and Serum in Kacang Goats Supplemented with Inorganic Selenium and Iodine.

    Science.gov (United States)

    Aghwan, Z A; Alimon, A R; Goh, Y M; Nakyinsige, K; Sazili, A Q

    2014-04-01

    Fat and fatty acids in muscle and adipose tissues are among the major factors influencing meat quality particularly nutritional value and palatability. The present study was carried out to examine the effects of supplementing inorganic selenium (Se), iodine (I) and a combination of both on fatty acid compositions in serum, and supraspinatus (SS), longissimus lumborum (LL), and semitendinosus (ST) muscles in goats. Twenty-four, 7 to 8 months old, Kacang male goats with a mean live weight of 22.00±1.17 kg were individually and randomly assigned into four groups of six animals each for 100 d of feeding prior to slaughter. The animals were offered the same concentrate (basal) diet as 1% of body weight with ad libitum amount of fresh guinea grass. The four groups were as follows: T1 (control) - basal diet without supplementation; T2 - basal diet with 0.6 mg Se/kg DM; T3 - basal diet with 0.6 mg I/kg DM; T4 - basal diet with combination of 0.6 mg Se/kg DM and 0.6 mg I/kg DM. The major fatty acids (FAs) detected in the serum were palmitic (C16:0), stearic (C18:0), oleic (C18:1n9) and linoleic (C18:2n-6), while the major FAs in the selected muscles were C16:0, C18:0 and C18:1n9 acids. The main polyunsaturated fatty acids (PUFA) detected in muscles and serum were (CI8:2n-6), linolenic acid (C18:3n-3), and arachidonic acid (C20:4n-6). No significant differences (p>0.05) were observed in the concentration of total saturated fatty acids (SFA) among the four groups. PUFA concentrations in the goats supplemented with Se (T2) were significantly higher (pgoats of the control group (T1). The PUFA: SFA ratio was significantly higher in the animals supplemented with dietary Se (T2) than those of control ones (T1). It is concluded that dietary supplementation of inorganic Se increased the unsaturated fatty acids in muscle. The supplementation of iodine with or without Se had negligible effects on muscle fatty acid content of Kacang crossbred male goats.

  13. Reaction of Silane Alkoxide with Acid Anhydride as a Novel Synthetic Method for Organic-Inorganic Hybrid Materials

    Institute of Scientific and Technical Information of China (English)

    Masahiro Fujiwara

    2005-01-01

    @@ 1Introduction Sol-gel method is a potent method to produce new inorganic and organic-inorganic hybrid materials. The key step of this methodology is the hydrolysis of a metal alkoxide or other metal substrates such as acetylacetonates to form hydroxyl metal species, followed by their condensation to metal-oxygen-metal (M - O - M)bonds. In this process, the utilization of water, generally in excess, is essential and alcoholic solvents such as ethanol are often required to homogenize the solution when organic compounds coexist. As the common sol-gel method using water allows for limited uses of organic substrates due to their low solubility and stability in aqueous solution, modified variations of sol-gel method are required. Recently, some processes were reported for preparing metal oxides from metal alkoxides without the utilization of water.

  14. Validation study of a rapid colorimetric method for the determination of phytic acid and inorganic phosphorus from seeds

    OpenAIRE

    Dragičević Vesna D.; Sredojević Slobodanka D.; Perić Vesna A.; Nišavić Anika R.; Srebrić Mirjana B.

    2011-01-01

    Phytate, as an important mineral storage compound in seeds, is vital for seed/grain development; it is often considered to be an antinutritional substance. The objective of this study was to develop a rapid and inexpensive colorimetric method of measuring phytate and inorganic P (Pi) concentrations from maize, soybean and sunflower seed/grain extracts, by combining adequate precision and simplicity, ideal for breeders interested in improving simultaneously Pi and phytate levels. The inv...

  15. Response surface methodology to optimize gradient ion chromatographic separation of inorganic anions and organic acids in tobacco leaves

    Institute of Scientific and Technical Information of China (English)

    Rui Qi Wang; Na Ni Wang; Jia Jie Zhang; Yan Zhu

    2011-01-01

    The separation optimization of nine organic and inorganic anions in tobacco leaves using gradient ion chromatography by response surface methodology was investigated. In order to achieve this goal the usefulness of the chromatographic response function (CRF) for the evaluation of the two different chromatographic performance goals (resolution and analysis time) was tested. The experiments were performed according to a Box-Behnken design response surface experimental design.

  16. Speciation of selenoamino acids, selenonium ions and inorganic selenium by ion exchange HPLC with mass spectrometric detection and its application to yeast and algae

    DEFF Research Database (Denmark)

    Larsen, Erik Huusfeldt; Hansen, M.; Fan, T.

    2001-01-01

    Cation and anion exchange HPLC were used to separate a mixture of 12 selenium species comprising selenoamino acids, selenonium ions and inorganic selenium. The cationic species were separated from each other and from the co-injected anions using a cation exchange column with gradient elution...... by aqueous pyridinium formate at pH similar to 3 as the mobile phase. The anionic species were separated using an anion exchange column with isocratic elution by an aqueous salicylate-TRIS mobile phase at pH 8.5. The separated selenium species were detected as Se-80 by ICP-dynamic reaction cell (DRC...... acid extract of Chlorella algae contained dimethylselenonium propionate (DMSeP), which was verified by HPLC-ES-MS. Se-allylselenocysteine and selenoethionine was detected at the low ng g(-1) concentration level based on co-chromatography with the standard substances spiked to the algal extract....

  17. Research progress in inorganic-organic hybrid proton exchange membrane based on phosphonic(phosphoric) acid%膦(磷)酸基无机-有机杂化质子交换膜的研究进展

    Institute of Scientific and Technical Information of China (English)

    郭芷含; 沈春晖; 陈成; 孔更金

    2012-01-01

    综述了通过溶胶-凝胶法制备的质子交换膜(PEM),即膦(磷)酸基无机-有机杂化PEM的发展状况.对比分析了掺杂磷酸和键合膦酸无机-有机杂化膜的稳定性以及膦(磷)酸与聚硅氧烷网络结构的连接方式对膜性能的影响.对膦酸基无机.有机杂化膜的发展前景进行了展望.%The development of inorganic-organic hybrid proton exchange membrane(PEM) based on phosphonic(phosphoric) acid was summarized, which were prepared from organosiloxane by sol-gel method. The stability between inorganic-organic hybrid membranes doped phosphoric acid and inorganic-organic hybrid membranes chemically grafted phosphonic acid was compared, then effect of connection ways of phosphonic (phosphoric) acid with the polysiloxane network structure on the membrane performance was discussed. The prospect development of inorganic-organic hybrid membranes based on phosphoric acid was described.

  18. Real-time measurements of ammonia, acidic trace gases and water-soluble inorganic aerosol species at a rural site in the Amazon Basin

    Directory of Open Access Journals (Sweden)

    I. Trebs

    2004-01-01

    Full Text Available We measured the mixing ratios of ammonia (NH3, nitric acid (HNO3, nitrous acid (HONO, hydrochloric acid (HCl, sulfur dioxide (SO2 and the corresponding water-soluble inorganic aerosol species, ammonium (NH4+, nitrate (NO3-, nitrite (NO2-, chloride (Cl- and sulfate (SO42-, and their diel and seasonal variations at a pasture site in the Amazon Basin (Rondônia, Brazil. This study was conducted within the framework of LBA-SMOCC (Large Scale Biosphere Atmosphere Experiment in Amazonia - Smoke Aerosols, Clouds, Rainfall and Climate: Aerosols from Biomass Burning Perturb Global and Regional Climate. Sampling was performed from 12 September to 14 November 2002, extending from the dry season (extensive biomass burning activity, through the transition period to the wet season (background conditions. Measurements were made continuously using a wet-annular denuder (WAD in combination with a Steam-Jet Aerosol Collector (SJAC followed by suitable on-line analysis. A detailed description and verification of the inlet system for simultaneous sampling of soluble gases and aerosol compounds is presented. Overall measurement uncertainties of the ambient mixing ratios usually remained below 15%. The limit of detection (LOD was determined for each single data point measured during the field experiment. Median LOD values (3σ-definition were ≤0.015ppb for acidic trace gases and aerosol anions and ≤0.118ppb for NH3 and aerosol NH4+. Mixing ratios of acidic trace gases remained below 1ppb throughout the measurement period, while NH3 levels were an order of magnitude higher. Accordingly, mixing ratios of NH4+ exceeded those of other inorganic aerosol contributors by a factor of 4 to 10. During the wet season, mixing ratios decreased by nearly a factor of 3 for all compounds compared to those observed when intensive biomass burning took place. Additionally, N-containing gas and aerosol species featured pronounced diel variations. This is attributed to strong

  19. Real-time measurements of ammonia, acidic trace gases and water-soluble inorganic aerosol species at a rural site in the Amazon Basin

    Directory of Open Access Journals (Sweden)

    I. Trebs

    2004-02-01

    Full Text Available We measured the mixing ratios of ammonia (NH3, nitric acid (HNO3, nitrous acid (HONO, hydrochloric acid (HCl, sulfur dioxide (SO2 and the corresponding water-soluble inorganic aerosol species, ammonium (NH4+, nitrate (NO3, nitrite (NO2, chloride (Cl and sulfate (SO42−, and their diel and seasonal variations at a pasture site in the Amazon Basin (Rondônia, Brazil. This study was conducted within the framework of LBA-SMOCC (Large Scale Biosphere Atmosphere Experiment in Amazonia Smoke Aerosols, Clouds, Rainfall and Climate. Sampling was performed from 12 September to 14 November 2002, extending from the dry season (extensive biomass burning activity, through the transition period to the wet season (background conditions. Measurements were made continuously using a wet-annular denuder in combination with a Steam-Jet Aerosol Collector (SJAC followed by suitable on-line analysis. A detailed description and verification of the inlet system for simultaneous sampling of soluble gases and aerosol compounds is presented. Overall measurement uncertainties of the ambient mixing ratios usually remained below 15%. The limit of detection (LOD was determined for each single data point measured during the field experiment. Median LOD values (3σ-definition were ≤0.015 ppb for acidic trace gases and aerosol anions and ≤0.118 ppb for NH3 and aerosol NH4+. Mixing ratios of acidic trace gases remained below 1ppb throughout the measurement period, while NH3 levels were an order of magnitude higher. Accordingly, mixing ratios of NH4+ exceeded those of other inorganic aerosol contributors by a factor of 4 to 10. During the wet season, mixing ratios decreased by nearly a factor of 3 for all compounds compared to those observed when intensive biomass burning

  20. Combining pH and electrical conductivity measurements to improve titrimetric methods to determine ammonia nitrogen, volatile fatty acids and inorganic carbon concentrations.

    Science.gov (United States)

    Charnier, C; Latrille, E; Lardon, L; Miroux, J; Steyer, J P

    2016-05-15

    Volatile fatty acids (VFA), inorganic carbon (IC) and total ammonia nitrogen (TAN) are key variables in the current context of anaerobic digestion (AD). Accurate measurements like gas chromatography and infrared spectrometry have been developed to follow the concentration of these compounds but none of these methods are affordable for small AD units. Only titration methods answer the need for small plant monitoring. The existing methods accuracy was assessed in this study and reveals a lack of accuracy and robustness to control AD plants. To solve these issues, a new titrimetric device to estimate the VFA, IC and TAN concentrations with an improved accuracy was developed. This device named SNAC (System of titration for total ammonia Nitrogen, volatile fatty Acids and inorganic Carbon) has been developed combining the measurement of electrical conductivity and pH. SNAC were tested on 24 different plant samples in a range of 0-0.16 mol.L(-1) TAN, 0.01-0.21 mol.L(-1) IC and 0-0.04 mol.L(-1) VFA. The standard error was about 0.012 mol.L(-1) TAN, 0.015 mol.L(-1) IC and 0.003 mol.L(-1) VFA. The coefficient of determination R(2) between the estimated and reference data was 0.95, 0.94 and 0.95 for TAN, IC and VFA respectively. Using the same data, current methods based on key pH points lead to standard error more than 14.5 times higher on VFA and more than 1.2 times higher on IC. These results show that SNAC is an accurate tool to improve the management of AD plant.

  1. New blue-light-emitting ultralong [Cd(L)(TeO3)] (L = polyamine) organic-inorganic hybrid nanofibre bundles: their thermal stability and acidic sensitivity.

    Science.gov (United States)

    Yao, Hong-Bin; Li, Xiao-Bo; Yu, Shu-Hong

    2009-08-03

    A new type of blue-light-emitting ultralong [Cd(L)(TeO(3))] (L = ethylenediamine, diethylenetriamine) nanofibre bundle has been synthesised under reflux in a mixed solvent media. Inorganic Cd(TeO(3)) layers are assumed to exist in the structures and are connected by the organic amine molecules through the coordination between nitrogen atoms and cadmium ions. The composition and formulae of these hybrid materials, based on the proposed structures, have been identified through element analysis (EA), thermal gravity analysis (TGA) and energy dispersive spectra (EDS). The thermal stabilities and optical properties of these nanofibre bundles have been investigated. Thermal decomposition of [Cd(en)(TeO(3))] (en = ethylenediamine) and [Cd(DETA)(TeO(3))] (DETA = diethylenetriamine) at 450 degrees C allowed the formation of a mixture of CdTe and Cd(TeO(3)) phases, and a pure CdTe phase, respectively. In addition, this new kind of hybrid bundle, which demonstrates blue emission, was found to be sensitive to acids, and the emission intensity is strongly dependent on the acidity of the solutions, implying that these hybrid nanofibre bundles could be potentially applied as acid sensors.

  2. Chemical composition and acidity of size-fractionated inorganic aerosols of 2013-14 winter haze in Shanghai and associated health risk of toxic elements

    Science.gov (United States)

    Behera, Sailesh N.; Cheng, Jinping; Huang, Xian; Zhu, Qiongyu; Liu, Ping; Balasubramanian, Rajasekhar

    2015-12-01

    The severe winter haze episode that occurred in Shanghai from December 2013 to January 2014, characterized by elevated levels of particulate matter (PM), received considerable international attention because of its impacts on public health and disruption of day-to-day activities. To examine the characteristics of PM during this haze episode and to assess the chemistry behind formation of secondary inorganic aerosols (SIA) and associated health impacts due to exposure of toxic elements, we characterized eight water soluble inorganic (WSI) ions and twenty four trace elements in twelve size-fractionated PM (10 nm-9.9 μm). The average mass concentrations of coarse (1.8 μm < Dp < 9.9 μm), fine (Dp < 2.5 μm), ultrafine (0.01 μm < Dp < 0.10 μm) and nano (0.01 μm < Dp < 0.056 μm) particles during hazy days were 2.8, 5.2, 5.3 and 5.1 times higher than those during non-hazy days, respectively. The in-situ pH (pHIS), as predicted by the Aerosol Inorganic Model (AIM-IV) in all sizes of PM, was observed to be lower during hazy days (average of -0.64) than that during non-hazy days (average of -0.29); there was an increased acidity in haze aerosols. Based on the measured concentrations of particulate-bound toxic elements, health risk assessment was conducted, which revealed that the excess lifetime carcinogenic risk to individuals exposed to fine particles under haze events increased significantly (P < 0.05) to 69 ± 18 × 10-6 compared to non-hazy days (34 ± 10 × 10-6). The qualitative source attribution analysis suggested that the occurrence of haze could be due to a combination of increased emissions of PM from multiple anthropogenic sources followed by its accumulation under unfavourable meteorological conditions with lower mixing heights and less wind speeds and the formation of secondary aerosols.

  3. Phytochemical and Morphological Attributes of St. John’s Wort (Hypericum perforatum Affected by Organic and Inorganic Fertilizers; Humic Acid and Potassium Sulphate

    Directory of Open Access Journals (Sweden)

    Helaleh Sadat KABOLI FARSHCHI

    2014-09-01

    Full Text Available This experiment was designed to evaluate the effects of organic (liquid humic acid and inorganic (potassium sulphate on phytochemical and morphological attributes of St. John’s Wort (Hypericum perforatum. Thus, a research was conducted in a factorial experiment (3×3 based on completely randomized design with three replications. Treatments consisted of potassium sulphate (Kx at three concentrations (0, 60 and 100 Kg/h which were treated before flowering and humic acid (Hx at three concentrations (0, 20 and 40 L/h which were fertigated four times of 15-days intervals. Results showed that the plant stem height, number of flowering stems and number of flowers were significantly affected by simple effect of each fertilizers (p<0.01, while their interaction effect was not significant for the plants height. The highest contents of fresh and dry weight were achieved under the highest amounts of fertilizers (K100 and H40. The highest stem height, number of flowers and number of flowering stems also belonged to these treatments. Increment of applied fertilizers led to increase of obtained essential oils, so that application of these fertilizers simultaneously increased the essential oil content up to 6-fold. Regarding the antioxidant activity, applied fertilizers at their high levels showed significant effects on decrease of EC50, which means the increment of antioxidant activity of H. perforatum.

  4. Phytochemical and Morphological Attributes of St. John’s Wort (Hypericum perforatum Affected by Organic and Inorganic Fertilizers; Humic Acid and Potassium Sulphate

    Directory of Open Access Journals (Sweden)

    Helaleh Sadat KABOLI FARSHCHI

    2014-09-01

    Full Text Available This experiment was designed to evaluate the effects of organic (liquid humic acid and inorganic (potassium sulphate on phytochemical and morphological attributes of St. John’s Wort (Hypericum perforatum. Thus, a research was conducted in a factorial experiment (3×3 based on completely randomized design with three replications. Treatments consisted of potassium sulphate (Kx at three concentrations (0, 60 and 100 Kg/h which were treated before flowering and humic acid (Hx at three concentrations (0, 20 and 40 L/h which were fertigated four times of 15-days intervals. Results showed that the plant stem height, number of flowering stems and number of flowers were significantly affected by simple effect of each fertilizers (p<0.01, while their interaction effect was not significant for the plants height. The highest contents of fresh and dry weight were achieved under the highest amounts of fertilizers (K100 and H40. The highest stem height, number of flowers and number of flowering stems also belonged to these treatments. Increment of applied fertilizers led to increase of obtained essential oils, so that application of these fertilizers simultaneously increased the essential oil content up to 6-fold. Regarding the antioxidant activity, applied fertilizers at their high levels showed significant effects on decrease of EC50, which means the increment of antioxidant activity of H. perforatum.

  5. PLASMA SPRAYED Al₂O₃-13 WT.%TiO₂ COATING SEALED WITH ORGANIC-INORGANIC HYBRID AGENT AND ITS CORROSION RESISTANCE IN ACID ENVIRONMENT

    Directory of Open Access Journals (Sweden)

    Zehua Zhou

    2016-07-01

    Full Text Available A novel organic-inorganic hybrid material of γ-methacryloxypropyltrime-thoxysilane (KH570 -SiO₂ was fabricated by Sol-Gel method. The hybrid material was used as the sealing agent for the plasma sprayed Al₂O₃-13 wt.% TiO₂ coating. Infrared spectrum and grafted mechanism of the hybrid agent (HA were studied. Moreover, morphology and porosity, as well as characteristics of immersion plus electrochemical corrosion in acid environment of the coating with and without sealing treatment were evaluated, compared with those of the coating sealed with the conventional silicone resin agent (SRA. The results reveal that KH570 was successfully grafted onto the surface of SiO₂. The HA film sealed on the surface of the coating presents a little better quality than the SRA film. The porosities of the coatings after the sealing treatment decreased. Furthermore, the sealing treatment can improve efficiently the corrosion resistance of the coating in 5 vol.% HCl solution. The hybrid sealing agent can become a candidate for the plasma sprayed Al₂O₃-13 wt.% TiO₂ coating used in acid environment to overcome some disadvantages of organic agents such as severely environmental pollution.

  6. Influence of wastewater sludge treatment using combined peroxyacetic acid oxidation and inorganic coagulants re-flocculation on characteristics of extracellular polymeric substances (EPS).

    Science.gov (United States)

    Zhang, Weijun; Cao, Bingdi; Wang, Dongsheng; Ma, Teng; Xia, Hua; Yu, Dehong

    2016-01-01

    Extracellular polymeric substances (EPS) are highly hydrated biopolymers and play important roles in bioflocculation, floc stability, and solid-water separation processes. Destroying EPS structure will result in sludge reduction and release of trapped water. In this study, the effects of combined process of peracetic acid (PAA) pre-oxidation and chemical re-flocculation on morphological properties and distribution and composition of EPS of the resultant sludge flocs were investigated in detail to gain insights into the mechanism involved in sludge treatment. It was found that sludge particles were effectively solubilized and protein-like substances were degraded into small molecules after PAA oxidation. A higher degradation of protein-like substances was observed at acid environments under PAA oxidation. Microscopic analysis revealed that no integral sludge floc was observed after oxidation with PAA at high doses. The floc was reconstructed with addition of inorganic coagulants (polyaluminium chloride (PACl) and ferric chloride (FeCl3)) and PACl performed better in flocculation due to its higher charge neutralization and bridging ability. Combined oxidative lysis and chemical re-flocculation provide a novel solution for sludge treatment.

  7. Anticancer Activity of Ferulic Acid-Inorganic Nanohybrids Synthesized via Two Different Hybridization Routes, Reconstruction and Exfoliation-Reassembly

    Directory of Open Access Journals (Sweden)

    Hyoung-Jun Kim

    2013-01-01

    Full Text Available We have successfully prepared nanohybrids of biofunctional ferulic acid and layered double hydroxide nanomaterials through reconstruction and exfoliation-reassembly routes. From X-ray diffraction and infrared spectroscopy, both nanohybrids were determined to incorporate ferulic acid molecules in anionic form. Micrsocopic results showed that the nanohybrids had average particle size of 150 nm with plate-like morphology. As the two nanohybridization routes involved crystal disorder and random stacking of layers, the nanohybrids showed slight alteration in z-axis crystallinity and particle size. The zeta potential values of pristine and nanohybrids in deionized water were determined to be positive, while those in cell culture media shifted to negative values. According to the in vitro anticancer activity test on human cervical cancer HeLa cells, it was revealed that nanohybrids showed twice anticancer activity compared with ferulic acid itself. Therefore we could conclude that the nanohybrids of ferulic acid and layered double hydroxide had cellular delivery property of intercalated molecules on cancer cell lines.

  8. A Note on Fatty Acids Profile of Meat from Broiler Chickens Supplemented with Inorganic or Organic Selenium

    Science.gov (United States)

    del Puerto, Marta; Cabrera, M. Cristina

    2017-01-01

    This investigation evaluated, in broiler chickens Pectoralis and Gastrocnemius muscles, the effect of the dietary supplementation with sodium selenite (0.3 ppm) versus selenomethionine (0.3 ppm), on the fatty acids composition, lipids indices, and enzymes indexes for desaturase, elongase, and thioesterase. The selenium reduced, in both muscles, the content of atherogenic fatty acids, C14:0 and C16:0, while it increased the C18:1 level. On the other hand, selenium increased, in both muscles, the content of C18:3n3 and EPA, but not DPA and DHA. No selenium effect was detected for PUFA/SFA, n-6, n-3, n-6/n-3, and atherogenic and thrombogenic indices. As for the enzyme indexes, a selenium effect is only detected for thioesterase. Taken together, the results highlight the potential effect of dietary selenium, mainly selenomethionine, in the modulation of the composition of fatty acids in chicken meat, in particular, reducing the content of atherogenic fatty acids and increasing the health promoting n-3 PUFA. PMID:28194404

  9. Mechanical properties of PET composites using multi-walled carbon nanotubes functionalized by inorganic and itaconic acids

    Directory of Open Access Journals (Sweden)

    A. May-Pat

    2012-02-01

    Full Text Available Multi-walled carbon nanotubes (MWCNTs were oxidized by two different acid treatments and further functionalized with itaconic acid (IA. The functionalized MWCNTs were used to fabricate Poly(ethylene terephthalate (PET composites by melt mixing. The presence of functional groups on the surface of the treated MWCNTs was confirmed by infrared spectroscopy and thermogravimetric analysis. The MWCNTs oxidized with a concentrated mixture of HNO3 and H2SO4 exhibited more oxygen containing functional groups (OH, COOH but also suffer larger structural degradation than those oxidized by a mild treatment based on diluted HNO3 followed by H2O2. PET composites were fabricated using the oxidized-only and oxidized followed by functionalization with IA MWCNTs. PET composites fabricated with MWCNT oxidized by mild conditions showed improved tensile strength and failure strain, while harsh MWCNT oxidation render them overly brittle.

  10. Organic-inorganic hybrid materials based on polyaniline/TiO(2) nanocomposites for ascorbic acid fuel cell systems.

    Science.gov (United States)

    Ganesan, Raman; Gedanken, Aharon

    2008-10-29

    Polyaniline was grafted onto a mixture of rutile and anatase TiO(2) nanoparticles by in situ chemical oxidative polymerization. These nanocomposites were characterized by carbon, hydrogen and nitrogen (CHN) analysis, x-ray diffraction (XRD), Fourier transform infrared (FTIR), ultraviolet-visible (UV-vis), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analysis. FTIR and UV-vis confirm the formation of polyaniline on TiO(2) nanoparticles. The TEM shows that the composites consist of PANI and TiO(2) nanoparticles. Compared to the neat polyaniline, PANI/TiO(2) composites show a higher capacitance and also a higher activity per mass of polyaniline. Since the PANI/TiO(2) composites are stable during the electrooxidation of ascorbic acid, they can be used as an alternative catalyst for direct ascorbic acid fuel cells.

  11. An investigation of proton conductivity of binary matrices sulfonated polysulfone/polyvinyltriazole after doping with inorganic acids

    Indian Academy of Sciences (India)

    Serkan Sevinç; Sevim Ünügür Çelik; Ayhan Bozkurt

    2015-04-01

    As anhydrous proton conductive membranes, sulfonated polysulfone (SPSU) and polyvinyl triazole were studied as binary matrices. The sulfonation of polysulfone was performed with trimethylsilylchlorosulfonate and high degree of sulfonation (140%) was obtained. Ion exchange capacity of SPSU was determined as 3.05 mmol−1/g. The polymer electrolyte membranes were prepared by blending of sulfonated polysulfone with polyvinyl triazole and phosphoric acid. Fourier transform infrared spectroscopy confirmed the sulfonation of the polysulfone and the ionic interaction between sulfonic acid and triazole units. Thermogravimetric analysis showed that the polymer electrolyte membranes are thermally stable up to at least 150° C. Scanning electron microscopy analysis indicated the homogeneity of the ternary composites. The maximum proton conductivity has been measured as 3.63 × 10−4S cm−1 at 150° C.

  12. Inorganic Materials

    Science.gov (United States)

    Černý, Radovan

    The separation of compounds by inorganic/organic boundary is of less importance for the structure determination by diffraction methods. More important for the diffraction is how the atoms build up larger building units and the crystal itself. A molecular/non-molecular boundary is therefore relevant for the choice of a structure determination method. Non-molecular compounds - also called extended solids - are constructed by bonds that extend "infinitely" in three dimensions through a crystal. These non-molecular crystals usually crystallize with higher symmetries, and atoms often occupy special Wyckoff positions. A review of actual methodology is given first, and then highlights and pitfalls of structure determination from powder diffraction, its problems and their solutions are shown and discussed using selected examples.

  13. On-site Rapid Detection of Trace Non-volatile Inorganic Explosives by Stand-alone Ion Mobility Spectrometry via Acid-enhanced Evaporization

    OpenAIRE

    2014-01-01

    New techniques for the field detection of inorganic improvised explosive devices (IEDs) are urgently developed. Although ion mobility spectrometry (IMS) has been proved to be the most effective method for screening organic explosives, it still faces a major challenge to detect inorganic explosives owing to their low volatilities. Herein, we proposed a strategy for detecting trace inorganic explosives by thermal desorption ion mobility spectrometry (TD-IMS) with sample-to-sample analysis time ...

  14. Attachment of inorganic moieties onto aliphatic polyurethanes

    Directory of Open Access Journals (Sweden)

    Eliane Ayres

    2007-06-01

    Full Text Available Polyurethanes have been used in a series of applications due basically to their versatility in terms of controlling the behavior by altering basically the type of reagents used. However, for more specific and advanced applications, such as in membranes, biomaterials and sensors, well-organized and defined chemical functionalities are necessary. In this work, inorganic functionalities were incorporated into aliphatic polyurethanes (PU having different macromolecular architectures. Polyurethanes were synthesized using a polyether diol and dicyclohexylmethane 4,4' diisocyanate (H12-MDI. Polyurethanes having carboxylic acid groups were also produced by introducing 2,2- bis (hydroxymethyl propionic acid in the polymerization process. Inorganic functionalities were inserted into polyurethanes by reacting isocyanate end capped chains with aminopropyltriethoxysilane followed by tetraethoxysilane. PU having carboxylic acid groups yielded transparent samples after the incorporation of inorganic entities, as an evidence of smaller and better dispersed inorganic entities in the polymer network. FTIR and swelling measurements showed that polyurethanes having carboxylic acid groups had inorganic domains less packed, condensed and cross-linked when compared to polyurethanes with no carboxylic acid groups. Results also suggested that the progressive incorporation of inorganic moieties in both types of polyurethanes occurred in regions previously activated with inorganic functionalities, instead of by the creation of new domains. The temperatures of thermal decomposition and glass transition were also shifted to higher temperatures when inorganic functionalities were incorporated into polyurethanes.

  15. Time-resolved variations in the distributions of inorganic ions, carbonaceous components, dicarboxylic acids and related compounds in atmospheric aerosols from Sapporo, northern Japan during summertime

    Science.gov (United States)

    Pavuluri, Chandra Mouli; Kawamura, Kimitaka; Kikuta, Motomi; Tachibana, Eri; Aggarwal, Shankar G.

    2012-12-01

    To better understand time-resolved variations of water-soluble organic aerosols in the atmosphere, we collected atmospheric particles (TSP) every 3 h during summertime (8-10 August, 2005) in Sapporo, northern Japan. We measured inorganic ions, carbonaceous components, dicarboxylic acids, ketoacids and α-dicarbonyls in TSP. SO42- was found as the most abundant ionic species (57 ± 9% of total ions determined) followed by NH4+ and NO3-. However, none of the ionic species showed any diurnal trend throughout the campaign. Organic carbon (OC) ranged from 2.1 to 12.1 μg m-3 whereas elemental carbon (EC) was negligible in most of the samples (0.31 ± 0.56 μg m-3). Oxalic (C2) acid was the most abundant diacid species, followed by malonic (C3) and succinic (C4) acids. Water-soluble OC (WSOC), water-insoluble OC (WIOC) and OC as well as dominant diacids (C2-C4), total diacids, ketoacids and α-dicarbonyls did not show diurnal trend on 8 August, but they showed clear diurnal distributions during 9-10 August following the changes in ambient temperature (and radiation). Detailed analyses of time-resolved aerosols demonstrate that diurnal variations of organic aerosol compositions are caused by local in situ photochemical production, but are significantly superimposed by long-range atmospheric transport of aerosols, particularly when the air masses are enriched with emissions from higher plants and/or biomass burning, and their photochemical processing during the transport.

  16. Science Update: Inorganic Chemistry.

    Science.gov (United States)

    Rawls, Rebecca

    1981-01-01

    Describes areas of inorganic chemistry which have changed dramatically in the past year or two, including photochemistry, electrochemistry, organometallic complexes, inorganic reaction theory, and solid state chemistry. (DS)

  17. Recovery of vanadium from spent catalysts of sulfuric acid plant by using inorganic and organic acids: Laboratory and semi-pilot tests.

    Science.gov (United States)

    Erust, Ceren; Akcil, Ata; Bedelova, Zyuldyz; Anarbekov, Kuanysh; Baikonurova, Aliya; Tuncuk, Aysenur

    2016-03-01

    Catalysts are used extensively in industry to purify and upgrade various feeds and to improve process efficiency. These catalysts lose their activity with time. Spent catalysts from a sulfuric acid plant (main elemental composition: 5.71% V2O5, 1.89% Al2O3, 1.17% Fe2O3 and 61.04% SiO2; and the rest constituting several other oxides in traces/minute quantities) were used as a secondary source for vanadium recovery. Experimental studies were conducted by using three different leaching systems (citric acid with hydrogen peroxide, oxalic acid with hydrogen peroxide and sulfuric acid with hydrogen peroxide). The effects of leaching time, temperature, concentration of reagents and solid/liquid (S/L) ratio were investigated. Under optimum conditions (1:25 S/L ratio, 0.1 M citric acid, 0.1 M hydrogen peroxide, 50°C and 120 min), 95% V was recovered in the presence of hydrogen peroxide in citric acid leaching.

  18. Methods development for separation of inorganic anions, organic acids and bases, and neutral organic compounds by ion chromatography and capillary electrophoresis

    Energy Technology Data Exchange (ETDEWEB)

    Li, Jie [Iowa State Univ., Ames, IA (United States)

    1999-04-01

    A novel anion-exchange resin containing three amine groups was prepared by reaction of a chloromethylated polystyrene-divinylbenzene (PS-DVB) resin with diethylenetriamine. After being protonated by contact with an aqueous acid, this resin can be used for ion chromatographic separation of anions. The charge on the resins can be varied from +1 to +3 by changing the mobile phase pH. The selectivity of the new ion exchangers for various inorganic anions was quite different from that of conventional anion exchangers. The performance of this new anion exchanger was studied by changing the pH and the concentration of the eluent, and several different eluents were used with some common anions as testing analytes. Conductivity detection and UV-visible detection were applied to detect the anions after separation. The new resin can also be used for HPLC separation of neutral organic compounds. Alkylphenols and alkylbenzenes were separated with this new polymeric resin, and excellent separations were obtained under simple conditions. This report contains Chapter 1: General introduction and Chapter 6: General conclusions.

  19. Organic-skinned inorganic nanoparticles: surface-confined polymerization of 6-(3-thienylhexanoic acid bound to nanocrystalline TiO2

    Directory of Open Access Journals (Sweden)

    Saji Viswanathan

    2011-01-01

    Full Text Available Abstract There are many practical difficulties in direct adsorption of polymers onto nanocrystalline inorganic oxide surface such as Al2O3 and TiO2 mainly due to the insolubility of polymers in solvents or polymer agglomeration during adsorption process. As an alternative approach to the direct polymer adsorption, we propose surface-bound polymerization of pre-adsorbed monomers. 6-(3-Thienylhexanoic acid (THA was used as a monomer for poly[3-(5-carboxypentylthiophene-2,5-diyl] (PTHA. PTHA-coated nanocrystalline TiO2/FTO glass electrodes were prepared by immersing THA-adsorbed electrodes in FeCl3 oxidant solution. Characterization by ultraviolet/visible/infrared spectroscopy and thermal analysis showed that the monolayer of regiorandom-structured PTHA was successfully formed from intermolecular bonding between neighbored THA surface-bound to TiO2. The anchoring functional groups (-COOH of the surface-crawling PTHA were completely utilized for strong bonding to the surface of TiO2.

  20. Inorganic ions in ambient fine particles over a National Park in central India: Seasonality, dependencies between SO42-, NO3-, and NH4+, and neutralization of aerosol acidity

    Science.gov (United States)

    Kumar, Samresh; Sunder Raman, Ramya

    2016-10-01

    Twelve hour integrated ambient fine particles (PM2.5) were collected over an Van Vihar National Park (VVNP), in Bhopal, Central India. Samples were collected on filter substrates every-other-day for two years (2012 and 2013). In addition to PM2.5 mass concentration, water soluble inorganic ions (WSIIs) were also measured. Further, on-site meteorological parameters including temperature, wind speed, wind direction, relative humidity, rainfall and atmospheric pressure were recorded. During 2012, the average PM2.5 concentration was 40 ± 31 μgm-3 while during 2013 it was 48 ± 50 μgm-3. Further, in about 20% of the samples the 12 h integrated fine PM mass exceeded the daily (24 h) average standards (60 μgm-3). This observation suggests that the PM2.5 mass concentration at the study site is likely to be in violation of the National Ambient Air Quality Standard (NAAQS), India. During the study period the sum of three major ions (SO42-, NO3-, and NH4+) accounted for 19.4% of PM2.5 mass on average. Air parcel back trajectory ensembles revealed that emissions from thermal power plants were likely to be the main regional source of particulate SO42- and NO3- measured over VVNP. Further, local traffic activities appeared to have no significant impact on the concentrations of PM2.5 and its WSIIs constituents, as revealed by a day-of-the-week analysis. PM2.5 mass, SO42-, NO3-, and NH4+ showed a pronounced seasonal trend with winter (Jan, Feb) and post-monsoon (Oct, Nov, Dec) highs and pre-monsoon (Mar, Apr, May) and monsoon (Jun, Jul, Aug, Sep) lows, during both 2012 and 2013. Further, when the sum of SO42- and NO3- constituted greater than 90% of water soluble inorganic anions by mass, they were linearly dependent on one another and moderately anti-correlated (r2 = 0.60). The molar ratios of NH4+ and non-sea salt SO42- were examined to understand the aerosol neutralization mechanisms and particulate NO3- formation. An assessment of these ratios and subsequent analyses

  1. 玉蜀黍叶中氨基酸及无机元素的含量测定%Determination of Amino Acids and Inorganic Elements in the leaves of Zea mays L.

    Institute of Scientific and Technical Information of China (English)

    刘银燕; 杨晓虹; 陈滴; 王文娜; 孙琦; 杨锦竹

    2012-01-01

    对玉蜀黍叶中氨基酸和无机元素进行研究.采用日立835-50型氨基酸分析仪和ICP - AES法对玉蜀黍叶中氨基酸和无机元素进行了研究.结果表明,玉蜀黍叶中含有17种氨基酸和12种人体必需的无机元素.本研究为玉蜀黍叶的药用开发提供了参考依据.%To determine amino acids and inorganic elements in the leaves of zea mays L., amino acids in leaves of zea mays L. Were determined by the amino acid analyzer, and inorganic elements in leaves of zea mays L. Were determined by ICP-AES. The result showed thai there were 17 amino acids and 12 kind of inorganic elements in leaves of zea mays L., and it provide a basis for the medical exploitation oi the leaves of zea mays L..

  2. A field-deployable, chemical ionization time-of-flight mass spectrometer: application to the measurement of gas-phase organic and inorganic acids

    Directory of Open Access Journals (Sweden)

    T. H. Bertram

    2011-03-01

    Full Text Available We report a new field-deployable chemical ionization time-of-flight mass spectrometer (CI-TOFMS for the direct measurement of trace gases in the atmosphere. We apply the technique to the measurement of gas-phase inorganic and organic acids via negative-ion proton transfer, using acetate as the reagent ion. A novel high pressure interface, incorporating two RF-only quadrupoles is used to efficiently focus ions through four stages of differential pumping before analysis with a compact TOFMS. The high ion-duty cycle (>20% of the TOFMS, coupled to efficient production and transmission of ions in the high pressure interface results in a highly sensitive (>300 ions s−1 pptv−1 instrument capable of the fast measurement of atmospheric gases at trace levels. We demonstrate the efficient transfer and detection of both bare ions and ion-molecule clusters, and characterize the instrument during field measurements aboard the R/V Atlantis as part of the CalNex campaign during the spring of 2010. The in-field short-term precision is better than 5% at 1 pptv (pL/L, for 1-second averages. The detection limit (3σ, 1-second averages of the current version of the CI-TOFMS, as applied to the in situ detection of gas-phase acids, is limited by the magnitude and variability in the background determination and was determined to be 4 pptv.

  3. Noninvasive tagging of proteins with an inorganic chromophore. Selectivity of chloro(terpyridine)platinum(II) toward amino acids, peptides, and cytochromes c

    Energy Technology Data Exchange (ETDEWEB)

    Brothers, H.M. II; Kostic, N.M.

    1988-05-18

    The complex (Pt(trpy)Cl)/sup +/ exhibits unexpected selectivity toward amino acid side chains in cytochromes c from Candida krusei and bakers' yeast. Although kinetic studies with amino acids and peptides as entering ligands prove this complex to be completely selective toward thiol over imidazole, His-33 and His-39 residues (in both proteins) are labeled with greater yields than the Cys-102 residue (in the bakers' yeast protein). The binding sites are determined by peptide mapping and other methods. The Pt(trpy)/sup 2+/ tags are stable, and the protein derivatives are separated by cation-exchange chromatography. The (Pt(trpy)His)/sup 2+/ and (Pt(trpy)Cys)/sup +/ chromophores are easily detected and quantitated owing to their characteristic and strong UV-vis bands. Spectroscopic and electrochemical measurements show that labeling with the new reagent does not alter the structural and redox properties of the cytochromes c. The unexpected outcome of the protein labeling indicates that, contrary to the common assumption, Cys-102 is not exposed at the protein surface. Modification of this residue with various organic reagents and dimerization of the protein must be accompanied by a perturbation of the conformation, which makes Cys-102 accessible to the reagent or to another molecule of the protein. These predictions from the labeling study are confirmed subsequently by the crystallographic study of the iso-1 cytochrome c from bakers' yeast. The inorganic complex (Pt(trpy)Cl)/sup +/ differs from the other reagents for protein modification by its noninvasiveness, a property that may well render it useful as a probe of the protein surface. 59 refs., 2 figs., 4 tabs.

  4. Noncovalent interaction of polyethylene glycol with copper complex of ethylenediaminetetraacetic acid and its application in constructing inorganic nanomaterials.

    Science.gov (United States)

    Pan, Shu Zhen; Song, Le Xin; Chen, Jie; Du, Fang Yun; Yang, Jing; Xia, Juan

    2011-10-21

    In this study, we try to answer a fundamental question: what is the consequence of the noncovalent interaction between a polymer and a coordination compound? Here, polyethylene glycol (PEG-4000, PEG-b) and copper complex of ethylenediaminetetraacetic acid (H(2)CuY) were employed to solve this problem. A novel adduct (CEP) between H(2)CuY and PEG-b was prepared. Our results indicated several interesting findings. First, the introduction of H(2)CuY had no effect on the stacking structure of PEG-b but led to a large change in surface structure of the polymer. Second, there was a significant difference (117 K) in the maximum degradation temperature between the PEG and the CEP, suggesting that the noncovalent interaction can drastically improve the thermal stability of the PEG. Third, sintering experiments showed that H(2)CuY and CEP produced completely different decomposition products. The former formed Cu crystals in nitrogen and CuO in air, but the latter generated Cu and CuCl crystals with good crystallinity, respectively. Finally, three independent measurements: viscosity, conductivity and nuclear magnetic resonance in solution, provided useful information and insights from both sides of the noncovalent interaction. Probable interaction mechanisms and interaction sites were proposed. We consider that the current research could create the foundation for a new understanding of how the noncovalent adduct interaction between a metallic complex and a polymer relates to the change in physical and chemical properties of the adducted components.

  5. Compound-specific 15N analysis of amino acids in 15N tracer experiments provide an estimate of newly synthesised soil protein from inorganic and organic substrates

    Science.gov (United States)

    Charteris, Alice; Michaelides, Katerina; Evershed, Richard

    2015-04-01

    Organic N concentrations far exceed those of inorganic N in most soils and despite much investigation, the composition and cycling of this complex pool of SOM remains poorly understood. A particular problem has been separating more recalcitrant soil organic N from that actively cycling through the soil system; an important consideration in N cycling studies and for the soil's nutrient supplying capacity. The use of 15N-labelled substrates as stable isotope tracers has contributed much to our understanding of the soil system, but the complexity and heterogeneity of soil organic N prevents thorough compound-specific 15N analyses of organic N compounds and makes it difficult to examine any 15N-labelled organic products in any detail. As a result, a significant proportion of previous work has either simply assumed that since the majority of soil N is organic, all of the 15N retained in the soil is organic N (e.g. Sebilo et al., 2013) or subtracted 15N-labelled inorganic compounds from bulk values (e.g. Pilbeam et al., 1997). While the latter approach is more accurate, these methods only provide an estimate of the bulk 15N value of an extremely complex and non-uniformly labelled organic pool. A more detailed approach has been to use microbial biomass extraction (Brookes et al., 1985) and subsequent N isotopic analysis to determine the 15N value of biomass-N, representing the fraction of 15N assimilated by microbes or the 15N cycling through the 'living' or 'active' portion of soil organic N. However, this extraction method can only generate estimates and some lack of confidence in its validity and reliability remains. Here, we present an alternative technique to obtain a measure of the assimilation of an applied 15N substrate by the soil microbial biomass and an estimate of the newly synthesized soil protein, which is representative of the magnitude of the active soil microbial biomass. The technique uses a stable isotope tracer and compound-specific 15N analysis, but

  6. Effect of Organic and Inorganic Fertilizers on Nitrogen and Potassium Uptake and Yield of Sweet Corn Grown on an Acid Soil

    Directory of Open Access Journals (Sweden)

    Mohd. T. M. Yusuff

    2007-01-01

    Full Text Available A field study was carried with the following objectives: (i To investigate the effect of compost, N, and K fertilizers on selected chemical properties of Bekenu series (Tipik Tualemkuts, and (ii To investigate the effect of compost, N and K fertilizers on N and K uptake and yield of Masmadu variety cultivated on Bekenu series. Treatments evaluated were: (i No fertilization (T1, (ii Hundred percent inorganic fertilizer application (T2, (iii Eighty percent of N fertilizer plus twenty percent of N from compost application (T3, (iv Sixty percent of N fertilizer plus forty percent of N from compost (T4, and (v Application of hundred percent compost (T5. The experiment was conducted at the share farm of Universiti Putra Malaysia Bintulu Campus, Sarawak, Malaysia. The experimental design was a randomized complete block design (RCBD with 4 replications. Nitrogen and K were applied in the forms of urea (46 % N and muriate of potash (60 % K2O in split i.e., at 15 days after planting (DAP and 36 DAP, respectively. At 73 DAP, plants were harvested. The fresh weight of cobs excluding guard rows was recorded. Dry weight (stem and leaves, N, K, Ca, and Mg concentrations were determined by standard procedures. Soil sampling was done before and after fertilization. Soil total N was determined using the Kjeldahl method while exchangeable K, Ca, and Mg were extracted using the double acid method and their concentrations determined using atomic absorption spectrophotometry. Dry ashing method was used for the determination of K, Ca, and Mg concentrations in plant tissues while the Kjeldahl method was used to determine total N in plant tissues. The concentrations multiplied by the oven dried weight of roots and stem provided N, K, Ca and Mg uptake in these plant parts. T2, T3, T4 and T5 affected soil bulk density, CEC, pH, total N, exchangeable K, Ca and Mg. The dry weight of Masmadu leaf was not affected by fertilization and so was N and K uptake in this plant part

  7. Separate vaporisation of boric acid and inorganic boron from tungsten sample cuvette-tungsten boat furnace followed by the detection of boron species by inductively coupled plasma mass spectrometry and atomic emission spectrometry (ICP-MS and ICP-AES).

    Science.gov (United States)

    Kataoka, Hiroko; Okamoto, Yasuaki; Tsukahara, Satoshi; Fujiwara, Terufumi; Ito, Kazuaki

    2008-03-10

    Utilising extremely different vaporisation properties of boron compounds, the determination procedures of volatile boric acid and total boron using tungsten boat furnace (TBF) ICP-MS and TBF-ICP-AES have been investigated. For the determination of volatile boric acid by TBF-ICP-MS, tetramethylammonium hydroxide (TMAH, Me(4)NOH) was used as a chemical modifier to retain it during drying and ashing stages. As for the total boron, not only non-volatile inorganic boron such as boron nitride (BN), boron carbide (B(4)C), etc. but also boric acid (B(OH)(3)) was decomposed by a furnace-fusion digestion with NaOH to produce sodium salt of boron, a suitable species for the electrothermal vaporisation (ETV) procedure. The proposed method was applied to the analysis of various standard reference materials. The analytical results for various biological and steel samples are described.

  8. Determination of volatile organic acids and inorganic anions in pharmaceutical wastewater by ion chromatography%离子色谱法测定制药废水中挥发性有机酸及无机阴离子

    Institute of Scientific and Technical Information of China (English)

    王强; 王路光; 王靖飞; 李洪波

    2009-01-01

    An ion chromatographic method for simultaneous determination of volatile organic acids and inorganic anions in pharmacentical wastewater was developed, using NaOH as eluent, ion exchange column for separation, and thermal conductivity detector for detection. Eight volatile organic acids and inorganic anions in pharmaceutical wastewater were separated in 28.0 min. The recoveries were 85.9%~109.5% and RSDs were 2.9%~10.9%. The method can be used for analysis of volatile organic acids and inorganic anions in wastewater in the production of penicillin and vitamin C.%建立了以NaOH为淋洗液、离子交换色谱柱为分析柱、用电导检测器进行检测的制药废水中有机酸和无机阴离子的离子色谱分析方法.结果表明,在28.0 min内可以分离出废水中8种主要挥发性有机酸与无机阴离子.方法回收率为85.9%~109.5 %,相对标准偏差为2.9%~10.9%.该法可用于青霉素生产废水、VC生产废水等制药废水中有机酸和无机阴离子的快速、准确分析,结果令人满意.

  9. Inorganic nanomedicine--part 1.

    Science.gov (United States)

    Sekhon, Bhupinder S; Kamboj, Seema R

    2010-08-01

    Inorganic nanomedicine refers to the use of inorganic or hybrid nanomaterials and nanosized objects to achieve innovative medical breakthroughs for drug and gene discovery and delivery, discovery of biomarkers, and molecular diagnostics. Potential uses for fluorescent quantum dots include cell labeling, biosensing, in vivo imaging, bimodal magnetic-luminescent imaging, and diagnostics. Biocompatible quantum dot conjugates have been used successfully for sentinel lymph node mapping, tumor targeting, tumor angiogenesis imaging, and metastatic cell tracking. Magnetic nanowires applications include biosensing and construction of nucleic acids sensors. Magnetic cell therapy is used for the repair of blood vessels. Magnetic nanoparticles (MNPs) are important for magnetic resonance imaging, drug delivery, cell labeling, and tracking. Superparamagnetic iron oxide nanoparticles are used for hyperthermic treatment of tumors. Multifunctional MNPs applications include drug and gene delivery, medical imaging, and targeted drug delivery. MNPs could have a vital role in developing techniques to simultaneously diagnose, monitor, and treat a wide range of common diseases and injuries. From the clinical editor: This review serves as an update about the current state of inorganic nanomedicine. The use of inorganic/hybrid nanomaterials and nanosized objects has already resulted in innovative medical breakthroughs for drug/gene discovery and delivery, discovery of biomarkers and molecular diagnostics, and is likely to remain one of the most prolific fields of nanomedicine.

  10. Inorganic-organic hybrid membranes with anhydrous proton conduction prepared from 3-aminopropyltriethoxysilane and sulfuric acid by the sol-gel method.

    Science.gov (United States)

    Tezuka, Teruaki; Tadanaga, Kiyoharu; Hayashi, Akitoshi; Tatsumisago, Masahiro

    2006-12-27

    Inorganic-organic hybrid membranes with anhydrous proton conduction were prepared from 3-aminopropyltriethoxysilane and H2SO4 by the sol-gel method. The membrane has a unique structure: a hexagonal phase formed by the stacking of rodlike polysiloxanes with ion complexes of ammonium groups and HSO4- extruded outside. The membranes showed high conductivity of 2 x 10-3 S cm-1 at 200 degrees C under dry atmosphere. In the membrane, protons probably migrate through the outside of the rodlike polysiloxanes along hydrogen-bond chains formed among HSO4- anions.

  11. UTILITY OF ZEOLITES IN REMOVAL OF INORGANIC AND ORGANIC WATER POLLUTANTS

    Science.gov (United States)

    Zeolites are well known for their ion exchange, adsorption and acid catalysis properties. Different inorganic and organic pollutants have been removed from water at room temperature using various zeolites. Synthetic zeolite Faujasite Y has been used to remove inorganic pollutants...

  12. Biosynthetic inorganic chemistry.

    Science.gov (United States)

    Lu, Yi

    2006-08-25

    Inorganic chemistry and biology can benefit greatly from each other. Although synthetic and physical inorganic chemistry have been greatly successful in clarifying the role of metal ions in biological systems, the time may now be right to utilize biological systems to advance coordination chemistry. One such example is the use of small, stable, easy-to-make, and well-characterized proteins as ligands to synthesize novel inorganic compounds. This biosynthetic inorganic chemistry is possible thanks to a number of developments in biology. This review summarizes the progress in the synthesis of close models of complex metalloproteins, followed by a description of recent advances in using the approach for making novel compounds that are unprecedented in either inorganic chemistry or biology. The focus is mainly on synthetic "tricks" learned from biology, as well as novel structures and insights obtained. The advantages and disadvantages of this biosynthetic approach are discussed.

  13. Changes in free amino acid content and activities of amination and transamination enzymes in yeasts grown on different inorganic nitrogen sources, including hydroxylamine.

    Science.gov (United States)

    Norkrans, B; Tunblad-Johansson, I

    1981-01-01

    This study concerns inter- and intraspecific differences between yeasts at assimilation of different nitrogen sources. Alterations in the content of free amino acids in cells and media as well as in the related enzyme activities during growth were studied. The hydroxylamine (HA)-tolerant Endomycopsis lipolytica was examined and compared with the nitrate-reducing Cryptococcus albidus, and Saccharomyces cerevisiae, requiring fully reduced nitrogen for growth. Special attention was paid to alanine, aspartic acid, and glutamic acid, the amino acids closely related to the Krebs cycle keto acids. The amino acids were analyzed as their n-propyl N-acetyl esters by gas-liquid chromatography (GLC). The composition of the amino acid pool was similar for the three yeasts. Glutamic acid was predominant; in early log-phase cells of E. lipolytica contents of 200-234 micromol . g(-1) dry weight were found. A positive correlation between the specific growth rate and the size of the amino acid pool was observed. The assimilation of ammonia was mediated by glutamate dehydrogenase (GDH). The NADP-GDH was the dominating enzyme in all three yeasts showing the highest specific activity in Cr. albidus grown on nitrate (6980 nmol . (min(-1)).(mg protein(-1)). Glutamine synthetase (GS) displayed a high specific activity in S. cerevisiae, which also had a high amount of glutamine. The assimilation of HA did not differ greatly from the assimilation of ammonium in E. lipolytica. The existing differences could rather be explained as provoked by the concentration of available nitrogen.

  14. Effects of in-feed inclusion of clinoptilolite on blood serum concentrations of aluminium and inorganic phosphorus and on ruminal pH and volatile fatty acid concentrations in dairy cows.

    Science.gov (United States)

    Karatzia, Maria A; Pourliotis, Konstantinos; Katsoulos, Panagiotis D; Karatzias, Harilaos

    2011-08-01

    The experiment investigated the effects of the dietary inclusion of 200 g of the natural zeolite, clinoptilolite on the blood serum concentrations of aluminium (Al) and inorganic phosphorus (P) as well as on the ruminal pH and the ruminal concentrations of Al and P and of certain volatile fatty acids. Sixteen Holstein cows with a rumen fistula were randomly assigned to one of two groups. Group A cows (n = 8) were fed the basal ration supplemented with 200 g of clinoptilolite per day, and group B cows (n = 8) were fed the basal ration and served as controls. Blood and rumen fluid samples were collected at the same day of each week and at the same time (5 h after morning feeding) for 12 weeks. Clinoptilolite supplementation had no significant effect on ruminal and blood serum concentrations of Al and P. However, clinoptilolite significantly increased ruminal pH and acetate, and decreased ruminal propionate and valerate.

  15. Science Update: Inorganic Chemistry

    Science.gov (United States)

    Rawls, Rebecca

    1978-01-01

    This first in a series of articles describing the state of the art of various branches of chemistry reviews inorganic chemistry, including bioinorganic, photochemistry, organometallic, and solid state chemistries. (SL)

  16. Inorganic Coatings Laboratory

    Data.gov (United States)

    Federal Laboratory Consortium — The inorganic Coatings Lab provides expertise to Navy and Joint Service platforms acquisition IPTs to aid in materials and processing choices which balance up-front...

  17. Spatial and seasonal variability of PM2.5 acidity at two Chinese megacities: insights into the formation of secondary inorganic aerosols

    Directory of Open Access Journals (Sweden)

    Z. Shi

    2012-02-01

    Full Text Available Aerosol acidity is one of the most important parameters influencing atmospheric chemistry and physics. Based on continuous field observations from January 2005 to May 2006 and thermodynamic modeling, we investigated the spatial and seasonal variations in PM2.5 acidity in two megacities in China, Beijing and Chongqing. Spatially, PM2.5 was generally more acidic in Chongqing than in Beijing, but a reverse spatial pattern was found within the two cities, with more acidic PM2.5 at the urban site in Beijing whereas the rural site in Chongqing. Ionic compositions of PM2.5 revealed that it was the higher concentrations of NO3− at the urban site in Beijing and the lower concentrations of Ca2+ within the rural site in Chongqing that made their PM2.5 more acidic. Temporally, PM2.5 was more acidic in summer and fall than in winter, while in the spring of 2006, the acidity of PM2.5 was higher in Beijing but lower in Chongqing than that in 2005. These were attributed to the more efficient formation of nitrate relative to sulfate as a result of the influence of Asian desert dust in 2006 in Beijing and the greater wet deposition of ammonium compared to sulfate and nitrate in 2005 in Chongqing. Furthermore, simultaneous increase of PM2.5 acidity was observed from spring to early summer of 2005 in both cities. This synoptic-scale evolution of PM2.5 acidity was accompanied by the changes in air masses origins, which were influenced by the movements of a subtropical high over the northwestern Pacific in early summer. Finally, the correlations between [NO3−]/[SO42−] and [NH4+]/[SO42−] suggests that under conditions of high aerosol acidity, heterogeneous reactions became one of the major pathways for the formation of nitrate at both cities. These findings provided new insights in our understanding of the spatial and temporal variations in aerosol acidity in Beijing and Chongqing, as well as those reported in other cities in China.

  18. Technical Study on Manufacturing Organic-inorganic Compound Fertilizer by Activating Humic Acid%活化腐植酸制备有机-无机复混肥的工艺研究

    Institute of Scientific and Technical Information of China (English)

    王家盛; 张伟; 石学勇; 苏州; 程颖

    2012-01-01

    Abstract: There are much humic acid in weathered coal and brown coal, but most of them are solidified by Ca2+ and Mg2+ in the nature, only be quite little water-soluble humic acid which can be directly absorbed by plants. Thus, it is necessary to make an activation to the hurnic acid. This paper study on how to use sodium bicarbonate and ammonia activate humic acid in order to receive a high biologic-active humic ammonia, which could as the organic material to blend with abio nutrient and producing granular organic-inorganic compound fertilizer. It is proved that the activate fer- tilizer sample obviously excelled than the unactivate one in chemical and phical parameters.%风化煤、褐煤等物质中含有大量的腐植酸,但在自然界中多数被钙、镁离子固定,能被作物直接吸收利用的水溶性腐植酸普遍含量甚微。因此,生产腐植酸肥料时,有必要进行腐植酸活化处理。本文研究了碳铵与氨水联合对褐煤进行活化处理,得到了生物活性较高的腐植酸铵,并以腐植酸铵作为有机原料与无机养分复混造粒制备了25-5-10有机-无机复混肥样品,经过性能指标和外观效果等方面的评价,明显优于未经活化的褐煤制得的样品。

  19. Intercalation compounds involving inorganic layered structures

    Directory of Open Access Journals (Sweden)

    CONSTANTINO VERA R. L.

    2000-01-01

    Full Text Available Two-dimensional inorganic networks can shown intracrystalline reactivity, i.e., simple ions, large species as Keggin ions, organic species, coordination compounds or organometallics can be incorporated in the interlayer region. The host-guest interaction usually causes changes in their chemical, catalytic, electronic and optical properties. The isolation of materials with interesting properties and making use of soft chemistry routes have given rise the possibility of industrial and technological applications of these compounds. We have been using several synthetic approaches to intercalate porphyrins and phthalocyanines into inorganic materials: smectite clays, layered double hydroxides and layered niobates. The isolated materials have been characterized by elemental and thermal analysis, X-ray diffraction, surface area measurements, scanning electronic microscopy, electronic and resonance Raman spectroscopies and EPR. The degree of layer stacking and the charge density of the matrices as well their acid-base nature were considered in our studies on the interaction between the macrocycles and inorganic hosts.

  20. The effectiveness of organic PCM based on lauric acid from coconut oil and inorganic PCM based on salt hydrate CaCl2.6H2o as latent heat energy storage system in Indonesia

    Science.gov (United States)

    U, Sri Rahayu A.; Putri, Widya A.; Sutjahja, I. M.; Kurnia, D.; Wonorahardjo, S.

    2016-08-01

    A latent heat energy storage system utilizing phase change materials (PCM) is an alternative strategy to reduce the use of Air Conditioning (AC) system in big cities in Indonesia in order for energy conservation in the future. In this research we used two kinds of materials, namely organic PCM based on lauric acid from coconut oil (CO) and inorganic PCM based on salt hydrate CaCl2.6H2O, because they have thermophysical parameters suitable for human's thermal comfort application in the building. The CO which contained more than 50% lauric acid has the melting temperature (Tm ) of about 26 °C and heat entalphy (ΔH) around 103 kJ/kg, while CaCl2.6H2O has the melting point of 29 °C and heat entalphy of 190 kJ/kg. In this paper we report the effectiveness of those two kinds of PCM in reducing the air temperature as one of some criteria for human's thermal comfort. The experiments were performed in a close and adiabatic room and the time-temperature measurements were done automatically using Arduino microcontroller and LM35 temperature sensor connected to the PC.

  1. Microfluidics in inorganic chemistry.

    Science.gov (United States)

    Abou-Hassan, Ali; Sandre, Olivier; Cabuil, Valérie

    2010-08-23

    The application of microfluidics in chemistry has gained significant importance in the recent years. Miniaturized chemistry platforms provide controlled fluid transport, rapid chemical reactions, and cost-saving advantages over conventional reactors. The advantages of microfluidics have been clearly established in the field of analytical and bioanalytical sciences and in the field of organic synthesis. It is less true in the field of inorganic chemistry and materials science; however in inorganic chemistry it has mostly been used for the separation and selective extraction of metal ions. Microfluidics has been used in materials science mainly for the improvement of nanoparticle synthesis, namely metal, metal oxide, and semiconductor nanoparticles. Microfluidic devices can also be used for the formulation of more advanced and sophisticated inorganic materials or hybrids.

  2. Inorganic contaminants attenuation in acid mine drainage by fly ash and fly ash-ordinary Portland cement (OPC) blends : column experiments

    Energy Technology Data Exchange (ETDEWEB)

    Gitari, W.M. [Venda Univ., Thohoyandou (South Africa). Dept. of Ecology and Resources Management, School of Environmental Studies; Petrik, L.F.; Etchebers, O. [Western Cape Univ., Bellville (South Africa). Environmental and Nanosciences Group, Dept. of Chemistry; Key, D.L. [Western Cape Univ., Bellville (South Africa). Dept. of Chemistry; Okujeni, C. [Western Cape Univ., Bellville (South Africa). Dept. of Earth Sciences

    2010-07-01

    The infiltration of acid mine drainage (AMD) material into mine voids is one of the environmental impacts of underground coal mining. In this study, the mitigation of AMD in a mine void was simulated in laboratory conditions. Various mixtures of fly ash, solid residues, and Portland cement were added to packed columns over a 6-month period. The fly ash additions generated near-neutral to alkaline pH levels, which in turn induced precipitation, co-precipitation, and adsorption contaminant attenuation mechanisms. A modelling study demonstrated that the precipitation of ferrihydrite, Al-hydroxides, Al-oxyhydroxysulphates, gypsum, ettringite, manganite, and rhodochrosite lowered contaminant levels. Results of the study indicated that the pH regime and acidity level of the AMD strongly influenced both the leaching of the toxic trace elements as well as the attenuation of the AMD. 3 refs., 2 figs.

  3. Geological and Inorganic Materials.

    Science.gov (United States)

    Jackson, L. L.; And Others

    1989-01-01

    Presents a review focusing on techniques and their application to the analysis of geological and inorganic materials that offer significant changes to research and routine work. Covers geostandards, spectroscopy, plasmas, microbeam techniques, synchrotron X-ray methods, nuclear activation methods, chromatography, and electroanalytical methods.…

  4. Synthesis of molecularly imprinted organic-inorganic hybrid azobenzene materials by sol-gel for radiation induced selective recognition of 2,4-dichlorophenoxyacetic acid

    Science.gov (United States)

    Shuai Jiang, Guang; An Zhong, Shi; Chen, Lan; Blakey, Idriss; Whitaker, Andrew

    2011-02-01

    A novel photoresponsive functional monomer bearing a siloxane polymerisable group and azobenzene moieties was synthesized. This monomer was then used to prepare photoresponsive molecularly imprinted polymers (MIP), which have specific binding sites for 2,4-dichlorophenoxyacetic acid (2,4-D) through hydrogen bonding moieties. The binding affinity of the imprinted recognition sites was switchable by alternate irradiations with ultraviolet and visible light, suggesting that azobenzene groups located inside the binding sites could be used as chemical sensors and the trans-cis isomerization could regulate the affinity for the 2,4-D. In addition, the concentration of the 2,4-D was able to be quantified by monitoring the trans-to-cis photoisomerization rate constant.

  5. Capillary ion electrophoresis of inorganic anions and uric acid in human saliva using a polyvinyl alcohol coated capillary column and hexamethonium chloride as additive of background electrolyte.

    Science.gov (United States)

    Mori, Masanobu; Yamamoto, Tsukasa; Kaseda, Maki; Yamada, Sachiko; Itabashi, Hideyuki

    2012-03-01

    A combination of polyvinyl alcohol chemically coated capillary (PVA capillary) and background electrolyte (BGE) with ion-pair reagent (hexamethonium dichloride, HMC) was used on capillary ion electrophoresis-UV detection (CIE-UV) for analysis of Br⁻, I⁻, NO₂⁻, NO₃⁻, SCN⁻ and uric acid in human saliva. The PVA capillary prepared in our laboratory minimized electro-osmotic flow (EOF) at the BGE in pH 3-10, and did not affect the UV detection at 210 nm by the PVA-layer on capillary wall. Therefore, use of the PVA capillary was suitable for sensitive UV detection for analyte anions, as well as suppression of protein adsorption. In this study, we optimized the BGE of 10 mM phosphate plus 10 mM HMC with applying a voltage of -15 kV. HMC as an additive to BGE could manipulate the electrophoretic mobility of anions, without electrostatic adsorption to the PVA capillary. The CIE-UV could separate and determine analyte anions in human saliva containing proteins by the direct injection without pretreatments such as dilution or deproteinization within 13 min. The relative standard deviations (n=10) were ranged of 0.5-1.6% in migration times, 2.2-6.8% in peak heights and 2.8-8.4% in peak areas. The limits of detection (S/N=3) were ranged of 3.42-6.87 μM. The peak height of anions in this system was gradually decreased through the successive injections of saliva samples, but the problem was successfully solved by periodically conditioning the PVA capillary. The quantifiability of anions in human saliva samples by the CIE-UV was evaluated through the recoveries by standard addition methods and comparison of other representative analytical methods, as well as identification by ion chromatography (IC). From the anion analyses in 12 different saliva samples, the CIE-UV demonstrated that can obtain obvious differences in concentrations of SCN⁻ between of smoker and non-smoker and those of uric acid between male and female with satisfactory results.

  6. Inorganic Analytical Chemistry

    DEFF Research Database (Denmark)

    Berg, Rolf W.

    The book is a treatise on inorganic analytical reactions in aqueous solution. It covers about half of the elements in the periodic table, i.e. the most important ones : H, Li, B, C, N, O, Na, Mg, Al, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Br, Sr, Mo, Ag, Cd, Sn, Sb, I, Ba, W,...

  7. [Influence of inorganic ions and humic acid on the removal of Pb(II) and Hg(II) in water by zero-valent iron].

    Science.gov (United States)

    Shi, Qiu-Ling; Zhou, Xin; Zhang, Jin-Zhong; Qiu, Xin-Kai

    2014-08-01

    The effects of Ca2+, Cl- and humic acid (HA) on the removal rates of Pb(II) and Hg(II) in water by zero-valent (ZVI) and the kinetic characteristics were studied, and the removal mechanism of Pb(II) and Hg(II) by ZVI were preliminarily investigated using X-ray diffraction (XRD). The results indicated that the removal mechanism of Pb(II) might mainly be attributed to the adsorption and co-precipitation of ZVI, while that of Hg(II) might mainly be attributed to the oxidation-reduction of ZVI. With the increase of Ca2+ concentration, the removal rates of Hg(II) and Pb(II) showed the trends of gradual increase and slight decrease, respectively. The Hg(II) removal increased with increasing Cl- concentration, whereas no obvious increase in Pb(II) removal was observed. The removal rates of Hg(II) and Pb(II) showed the trends of slow increase and slow decrease with increasing HA concentration, respectively. When Ca2+, Cl- and HA coexisted, the removal rates of Hg(II) and Pb(II) reached 99.71% and 97.95%, respectively. The removal processes of Pb(II) and Hg(II) could be described by pseudo first-order reaction kinetic equations when Ca2+, Cl- and HA existed alone and in combination. The removal rate constant of Pb(II) was the maxinum (0.024 0 min(-1)) when 5 mg x L(-1) HA existed alone, whereas that of Hg(II) was the maximum (0.0169 min(-1)) when 0.80 mmol x L(-1) Ca2+ existed alone.

  8. Ionic Transfer in Hybrid Inorganic/Organic Membranes

    Institute of Scientific and Technical Information of China (English)

    A.B.Yaroslavtsev; I.A.Stenina; A.S.Shalimov

    2007-01-01

    1 Results In last years increasing interest has been devoted to the development and research of transport properties of hybrid organic/inorganic membranes. Traditionally, these membranes are used as electrolyte in fuel cells. However a number of their properties allow considering them as perspective materials for water treatment and substance purification. In this work transport properties of some ion exchange membranes modified by inorganic nanoparticles (hydrated oxides or solid acids) are discussed. ...

  9. Simultaneous determination of organic acids and inorganic anions in Danshen for injection (lyophilized powder) by ion chromatography%离子色谱法同时测定注射用丹参(冻干)中有机酸和无机阴离子

    Institute of Scientific and Technical Information of China (English)

    刘静; 李静; 聂黎行; 王钢力; 王英新; 林瑞超

    2012-01-01

    Objective: To establish an ion chromatography method for simultaneous determination of five organic acids (lactic acid, acetic acid, formic acid, succinic acid and oxalic acid) and two inorganic anions ( chloridion and nitrate) in Danshen for injection(lyophilized powder). Methods;Five organic acids and two inorganic anions were determined by anion exchange column Ion Pac ASH -HC,eluted by gradient hydroxide potassium(1 -50 mmol · L-1 ) and identified by suppressed conductivity detector ASRS 300 with self - circulation suppression mode. Results ; Good resolution can be achieved among the above mentioned five organic acids and two inorganic anions. Their linear correlations over the investigated concentration were in the range of 0. 9996 - 0. 9999 and 0. 9997 -0. 9999,while the average recoveries were 92. 4% - 105. 1% and 102. 0% - 103. 2% .respectively. Conclusion: The ion chromatography method is fast, accurate, simple, reliable and applicable for the assay and quality control of organic acids and inorganic anions in Danshen for injection(lyophilized powder).%目的:建立能够同时测定注射用丹参(冻干)中有机酸(乳酸、乙酸、甲酸、琥珀酸和草酸)和无机阴离子(氯离子和硝酸根离子)含量的离子色谱法.方法:以Ion Pac AS11-HC阴离子交换柱分离,1~50 mmol·L-1氢氧化钾溶液梯度淋洗,ASRS300型抑制器电导检测器检测,自循环抑制模式.结果:5个有机酸及2个无机阴离子基本达到分离,线性关系良好,相关系数分别在0.9996~0.9999和0.9997~0.9999,平均回收率分别在92.4%~105.1%和102.0% ~ 103.2%.结论:所建立的方法快速、准确、简便、实用,可用于注射用丹参(冻干)中有机酸和无机阴离子的含量测定和质量控制.

  10. 无机金属盐对微波辅助酸预处理毛竹酶解的影响%Effect of Inorganic Salts on Enzymatic Saccharification of Moso Bamboo Pretreated by Microwave-Dilute Acid

    Institute of Scientific and Technical Information of China (English)

    李志强; 费本华; 江泽慧

    2014-01-01

    采用加入无机金属盐的稀酸溶液预处理毛竹,分析预处理后底物的化学组成、预处理后的废液组成、糖降解发酵抑制物的生成量等。结果表明:稀酸预处理主要以脱除半纤维素为主,而对木质素的脱除没有明显效果。当硫酸用量为2%( w/w)、预处理温度为180℃时,竹材中绝大部分半纤维素已被脱除,底物纤维素转化为葡萄糖的收率可达52.72%。加入硫酸铁催化后的稀酸预处理能提高底物的酶水解性能,可使纤维素转化为葡萄糖的收率提高到72.15%。硫酸钠、硫酸亚铁、硫酸铜和硼砂等催化后的稀酸预处理底物的酶水解性能均有不同程度的下降,其中以硫酸铜催化预处理底物的酶水解性能最差。铜离子在预处理中可以被竹材底物吸附,并且在酶水解过程中可以脱附进入水解液中。%Global warming and energy shortage are the main challenges and puzzles that government and the public around the world are facing. It is believed that one of the solutions is to use biomass as a potential renewable energy resource for producing liquid fuels such as bioethanol and biodiesel. Bamboo,with cellulose and hemicellulose as its main components,is a kind of fast growth and cheap renewable resource for bioethanol production. In the study,inorganic salts were studied as promoter in the dilute acid pretreatment of moso bamboo for the enzymatic saccharification. The chemical composition of the substrates and spent liquors,the enzymatic hydrolyability of substrates were analyzed. The results showed that dilute acid pretreatment ( DA) enhances the digestibility of lignocellulose mainly by dissolving hemicellulose and partially prehydrolyzing cellulose. DA has no delignified. The cellulose-to-glucose conversion yield of 2% sulfuric acid( w/w) pretreated substrate was 52. 72%. Sulfuric acid with Fe2 ( SO4 ) 3 pretreated substrate had the higher cellulose-to-glucose conversion yield

  11. Inorganic Crystal Structure Database (ICSD)

    Science.gov (United States)

    SRD 84 FIZ/NIST Inorganic Crystal Structure Database (ICSD) (PC database for purchase)   The Inorganic Crystal Structure Database (ICSD) is produced cooperatively by the Fachinformationszentrum Karlsruhe(FIZ) and the National Institute of Standards and Technology (NIST). The ICSD is a comprehensive collection of crystal structure data of inorganic compounds containing more than 140,000 entries and covering the literature from 1915 to the present.

  12. Selective inorganic thin films

    Energy Technology Data Exchange (ETDEWEB)

    Phillips, M.L.F.; Weisenbach, L.A.; Anderson, M.T. [Sandia National Laboratories, Albuquerque, NM (United States)] [and others

    1995-05-01

    This project is developing inorganic thin films as membranes for gas separation applications, and as discriminating coatings for liquid-phase chemical sensors. Our goal is to synthesize these coatings with tailored porosity and surface chemistry on porous substrates and on acoustic and optical sensors. Molecular sieve films offer the possibility of performing separations involving hydrogen, air, and natural gas constituents at elevated temperatures with very high separation factors. We are focusing on improving permeability and molecular sieve properties of crystalline zeolitic membranes made by hydrothermally reacting layered multicomponent sol-gel films deposited on mesoporous substrates. We also used acoustic plate mode (APM) oscillator and surface plasmon resonance (SPR) sensor elements as substrates for sol-gel films, and have both used these modified sensors to determine physical properties of the films and have determined the sensitivity and selectivity of these sensors to aqueous chemical species.

  13. Structural crystallography of inorganic oxysalts

    CERN Document Server

    Krivovichev, Sergey V

    2009-01-01

    Inorganic oxysalts are chemical compounds that contain oxygen - the most abundant element in the Earth's core. This book is the first systematic survey of structures of inorganic oxysalts considered from the viewpoint of modern scientific methods of description and visualisation of complex atomic arrangements.

  14. Ion-Conducting Organic/Inorganic Polymers

    Science.gov (United States)

    Kinder, James D.; Meador, Mary Ann B.

    2007-01-01

    Ion-conducting polymers that are hybrids of organic and inorganic moieties and that are suitable for forming into solid-electrolyte membranes have been invented in an effort to improve upon the polymeric materials that have been used previously for such membranes. Examples of the prior materials include perfluorosulfonic acid-based formulations, polybenzimidazoles, sulfonated polyetherketone, sulfonated naphthalenic polyimides, and polyethylene oxide (PEO)-based formulations. Relative to the prior materials, the polymers of the present invention offer greater dimensional stability, greater ease of formation into mechanically resilient films, and acceptably high ionic conductivities over wider temperature ranges. Devices in which films made of these ion-conducting organic/inorganic polymers could be used include fuel cells, lithium batteries, chemical sensors, electrochemical capacitors, electrochromic windows and display devices, and analog memory devices. The synthesis of a polymer of this type (see Figure 1) starts with a reaction between an epoxide-functionalized alkoxysilane and a diamine. The product of this reaction is polymerized by hydrolysis and condensation of the alkoxysilane group, producing a molecular network that contains both organic and inorganic (silica) links. The silica in the network contributes to the ionic conductivity and to the desired thermal and mechanical properties. Examples of other diamines that have been used in the reaction sequence of Figure 1 are shown in Figure 2. One can use any of these diamines or any combination of them in proportions chosen to impart desired properties to the finished product. Alternatively or in addition, one could similarly vary the functionality of the alkoxysilane to obtain desired properties. The variety of available alkoxysilanes and diamines thus affords flexibility to optimize the organic/inorganic polymer for a given application.

  15. Selective inorganic thin films

    Energy Technology Data Exchange (ETDEWEB)

    Phillips, M.L.F.; Pohl, P.I.; Brinker, C.J. [Sandia National Labs., Albuquerque, NM (United States)

    1997-04-01

    Separating light gases using membranes is a technology area for which there exists opportunities for significant energy savings. Examples of industrial needs for gas separation include hydrogen recovery, natural gas purification, and dehydration. A membrane capable of separating H{sub 2} from other gases at high temperatures could recover hydrogen from refinery waste streams, and facilitate catalytic dehydrogenation and the water gas shift (CO + H{sub 2}O {yields} H{sub 2} + CO{sub 2}) reaction. Natural gas purification requires separating CH{sub 4} from mixtures with CO{sub 2}, H{sub 2}S, H{sub 2}O, and higher alkanes. A dehydrating membrane would remove water vapor from gas streams in which water is a byproduct or a contaminant, such as refrigeration systems. Molecular sieve films offer the possibility of performing separations involving hydrogen, natural gas constituents, and water vapor at elevated temperatures with very high separation factors. It is in applications such as these that the authors expect inorganic molecular sieve membranes to compete most effectively with current gas separation technologies. Cryogenic separations are very energy intensive. Polymer membranes do not have the thermal stability appropriate for high temperature hydrogen recovery, and tend to swell in the presence of hydrocarbon natural gas constituents. The authors goal is to develop a family of microporous oxide films that offer permeability and selectivity exceeding those of polymer membranes, allowing gas membranes to compete with cryogenic and adsorption technologies for large-scale gas separation applications.

  16. Quest for new materials: Inorganic chemistry plays a crucial role

    Indian Academy of Sciences (India)

    J Gopalakrishnan; Rohini Mani

    2009-05-01

    There is an endless quest for new materials to meet the demands of advancing technology. Thus, we need new magnetic and metallic/semiconducting materials for spintronics, new low-loss dielectrics for telecommunication, new multi-ferroic materials that combine both ferroelectricity and ferromagnetism for memory devices, new piezoelectrics that do not contain lead, new lithium containing solids for application as cathode/anode/electrolyte in lithium batteries, hydrogen storage materials for mobile/transport applications and catalyst materials that can convert, for example, methane to higher hydrocarbons, and the list is endless! Fortunately for us, chemistry - inorganic chemistry in particular - plays a crucial role in this quest. Most of the functional materials mentioned above are inorganic non-molecular solids, while much of the conventional inorganic chemistry deals with isolated molecules or molecular solids. Even so, the basic concepts that we learn in inorganic chemistry, for example, acidity/basicity, oxidation/reduction (potentials), crystal field theory, low spin-high spin/inner sphere-outer sphere complexes, role of -electrons in transition metal chemistry, electron-transfer reactions, coordination geometries around metal atoms, Jahn-Teller distortion, metal-metal bonds, cation-anion (metal-nonmetal) redox competition in the stabilization of oxidation states - all find crucial application in the design and synthesis of inorganic solids possessing technologically important properties. An attempt has been made here to illustrate the role of inorganic chemistry in this endeavour, drawing examples from the literature as well as from the research work of my group.

  17. Inorganic materials in industrial processes

    OpenAIRE

    Demadis, Konstantinos

    2015-01-01

    Although inorganic materials represent a small number to the extreme number of the organic ones, they play a number of crucial roles in several processes of industrial interest. Two significant technologically processes have been selected as “case studies” for this presentation: metallic corrosion and its control, and mitigation of inorganic deposits, both related to industrial water systems. Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech.

  18. Essentials of inorganic materials synthesis

    CERN Document Server

    Rao, C N R

    2015-01-01

    This compact handbook describes all the important methods of synthesis employed today for synthesizing inorganic materials. Some features: Focuses on modern inorganic materials with applications in nanotechnology, energy materials, and sustainability Synthesis is a crucial component of materials science and technology; this book provides a simple introduction as well as an updated description of methods Written in a very simple style, providing references to the literature to get details of the methods of preparation when required

  19. [Studies on the assimilation of inorganic selenium by yeast].

    Science.gov (United States)

    Xie, L; Ouyang, Z; Xie, X

    1990-02-01

    In the process of assimilation of inorganic selenium by yeast to the organic-selenium, some rules on the relation of the kinds of culture medium, concentration of sodium selenite and methionine to the total selenium and selenomethionine content in the yeast formed have been found; and a new, accurate procedure--modified acid hydrolysis-ion exchange chromatography for determining the content of seleno-amino acid in biological materials has been established.

  20. Electricity generation from an inorganic sulfur compound containing mining wastewater by acidophilic microorganisms

    NARCIS (Netherlands)

    Ni, Gaofeng; Christel, Stephan; Roman, Pawel; Wong, Zhen Lim; Bijmans, Martijn F.M.; Dopson, Mark

    2016-01-01

    Sulfide mineral processing often produces large quantities of wastewaters containing acid-generating inorganic sulfur compounds. If released untreated, these wastewaters can cause catastrophic environmental damage. In this study, microbial fuel cells were inoculated with acidophilic microorganism

  1. Organic/inorganic hybrid coatings for anticorrosion

    Science.gov (United States)

    He, Zhouying

    Compared to organic coatings, organic-inorganic hybrid coatings can potentially improve the anticorrosion performance. The organic phase provides the excellent mechaincal and barrier properties while the inorganic phase acts as an adhesion promoter and corrosion inhibitor. Despite that many studies on alkoxylsilane-based hybrid coatings have been developed and studied, their weatherability and anticorrosion performance has been rarely evaluated. On the other hand, organic-inorganic hybrid coatings based on mixed sol-gel precursors have received much less attention compared to alkoxylsilane-based hybrid coatings. In the first part, polyurethane hybrid coatings with a unique hybrid crosslinked structure as an improved unicoat were successfully prepared. The effect of polyesters on physical properties of the hybrid coatings was studied. Polyurethane coatings derived from cycloaliphatic polyester show comparable properties than those derived from the commercially viable aromatic polyester. Introducing the polysiloxane part into the polyurethane coatings enhanced the crosslinking density, Tg, mechanical properties, and general coating properties. The increased adhesion between the hybrid coating and the substrate make the hybrid coating a good candidate for anticorrosion application, which is shown by electrochemical impedance spectroscopy (EIS). The degradation mechanism of the polyurethane/polysiloxane hybrid coatings under various weathering conditions was shown to be the scission of the urethane and ester groups in the organic phase along with reorganizing and rearranging of the inorganic phase. The anticorrosion performance of the cycloaliphatic hybrid was much better than that of aromatic based hybrid under outdoor weathering based on visual observation and EIS analysis. Acid undercutting is an issue for TEOS based hybrid coating. In the second part, design of experiments (DOEs) was used to statistically investigate on the effect of sol-gel precursors. The

  2. Semiconducting organic-inorganic nanocomposites by intimately tethering conjugated polymers to inorganic tetrapods

    Science.gov (United States)

    Jung, Jaehan; Yoon, Young Jun; Lin, Zhiqun

    2016-04-01

    Semiconducting organic-inorganic nanocomposites were judiciously crafted by placing conjugated polymers in intimate contact with inorganic tetrapods via click reaction. CdSe tetrapods were first synthesized by inducing elongated arms from CdSe zincblende seeds through seed-mediated growth. The subsequent effective inorganic ligand treatment, followed by reacting with short bifunctional ligands, yielded azide-functionalized CdSe tetrapods (i.e., CdSe-N3). Finally, the ethynyl-terminated conjugated polymer poly(3-hexylthiophene) (i.e., P3HT-&z.tbd;) was tethered to CdSe-N3 tetrapods via a catalyst-free alkyne-azide cycloaddition, forming intimate semiconducting P3HT-CdSe tetrapod nanocomposites. Intriguingly, the intimate contact between P3HT and CdSe tetrapod was found to not only render the effective dispersion of CdSe tetrapods in the P3HT matrix, but also facilitate the efficient electronic interaction between these two semiconducting constituents. The successful anchoring of P3HT chains onto CdSe tetrapods was substantiated through Fourier transform infrared spectroscopy and nuclear magnetic resonance spectroscopy measurements. Moreover, the absorption and photoluminescence studies further corroborated the intimate tethering between P3HT and CdSe tetrapods. The effect of the type of bifunctional ligands (i.e., aryl vs. aliphatic ligands) and the size of tetrapods on the device performance of hybrid organic-inorganic solar cells was also scrutinized. Interestingly, P3HT-CdSe tetrapod nanocomposites produced via the use of an aryl bifunctional ligand (i.e., 4-azidobenzoic acid) exhibited an improved photovoltaic performance compared to that synthesized with their aliphatic ligand counterpart (i.e., 5-bromovaleric acid). Clearly, the optimal size of CdSe tetrapods ensuring the effective charge transport in conjunction with the good dispersion of CdSe tetrapods rendered an improved device performance. We envision that the click-reaction strategy enabled by

  3. One step synthesis of silver nanorods by autoreduction of aqueous silver ions with hydroxyapatite: An inorganic-inorganic hybrid nanocomposite.

    Science.gov (United States)

    Arumugam, Sujatha K; Sastry, Thotapalli Parvathaleswara; Sreedhar, B; Mandal, Asit Baran

    2007-02-01

    In this report, a novel method for the synthesis of silver nanoparticles on the surface of hydroxyapatite is described. Hydroxyapatite crystals are synthesized from acid mineralized solution, a byproduct of bone glue industries, by a simple chemical precipitation method, which results in the formation of hydroxyapatite nanocrystals. The reduction of silver ions occurs by the electron transfer from the hydroxyl groups on the surface of hydroxyapatite. This results in the formation of silver nanorods and needle shaped nanoparticles that are bound on the surface of hydroxyapatite, and the observed silver nanocrystals show anisotropic structure. Thus, hydroxyapatite crystals can be used as a new class of inorganic scaffolds for the synthesis of nanomaterials with implications in designing inorganic-inorganic hybrid nanocomposites for different applications.

  4. Recent developments in Inorganic polymers: A Review with focus on Si-Al based inorganic polymers

    Directory of Open Access Journals (Sweden)

    Shrray Srivastava

    2015-12-01

    Full Text Available Inorganic polymers are a unique classification of polymers. They contain inorganic atoms in the main chain. Hybrids with organic polymers as well as those chains that contain metals as pendant groups are considered in a special sub-classification as organo-metallic polymers. The networks containing only inorganic elements in main chain are called inorganic polymers. The silicone rubber is the most commercial inorganic polymer. The organo-metallic and inorganic polymers have a different set of applications. The current paper is a review of current applications of polymers with inorganic back-bone networks, especially focusing on Si and Al based inorganic polymeric materials.

  5. Inorganic Reaction Mechanisms. Part I

    Science.gov (United States)

    Cooke, D. O.

    1976-01-01

    Provides a collection of data on the mechanistic aspects of inorganic chemical reactions. Wherever possible includes procedures for classroom demonstration or student project work. The material covered includes gas phase reactions, reactions in solution, mechanisms of electron transfer, the reaction between iron III and iodine, and hydrolysis. (GS)

  6. Carbon dioxide removal with inorganic membranes

    Energy Technology Data Exchange (ETDEWEB)

    Judkins, R.R.; Fain, D.E. [Oak Ridge National Laboratory, TN (United States)

    1993-12-31

    The increasing concentrations of greenhouse gases, particularly carbon dioxide, in the atmosphere has sparked a great deal of interest in the removal of CO{sub 2} from flue gases of fossil fueled plants. Presently, several techniques for the removal of CO{sub 2} are considered to have potential, but are lacking in practicality. For example, amine scrubbing of flue gas streams is potential, but are lacking in practically. For example, amine scrubbing of flue gas streams is effective in removing CO{sub 2}, but costs are high; efficiency suffers; and other acid gases must be removed prior to amine stripping. Membrane systems for CO{sub 2} removal are held in high regard, and inorganic, particularly ceramic, membranes offer the potential for high temperature, thus energy saving, removal.

  7. Organic/inorganic nanocomposite polymer electrolyte

    Institute of Scientific and Technical Information of China (English)

    Li Qi; Shao Jun Dong

    2007-01-01

    The organic/inorganic nanocomposites polymer electrolytes were designed and synthesized. The organic/inorganic nanocom posites membrane materials and their lithium salt complexes have been found thermally stable below 200 ℃. The conductivity of the organic/inorganic nanocomposites polymer electrolytes prepared at room temperature was at magnitude range of 10-6 S/cm.

  8. Inorganic ion composition in Tardigrada

    DEFF Research Database (Denmark)

    Halberg, Kenneth Agerlin; Larsen, Kristine Wulff; Jørgensen, Aslak;

    2013-01-01

    Many species of tardigrades are known to tolerate extreme environmental stress, yet detailed knowledge of the mechanisms underlying the remarkable adaptations of tardigrades is still lacking, as are answers to many questions regarding their basic biology. Here, we present data on the inorganic ion...... indicates that Na(+) and Cl(-) are the principle inorganic ions in tardigrade fluids, albeit other ions, i.e. K(+), NH(4)(+), Ca(2+), Mg(2+), F(-), SO(4)(2-) and PO(4)(3-) were also detected. In limno-terrestrial tardigrades, the respective ions are concentrated by a large factor compared......+) and F(-) are only slightly concentrated (×2-10). An anion deficit of ~120 mEq 1(-1) in M. tardigradum and H. crispae indicates the presence of unidentified ionic components in these species. Body fluid osmolality ranges from 361±49 mOsm kg(-1) in R. coronifer to 961±43 mOsm kg(-1) in H. crispae...

  9. Problems in structural inorganic chemistry

    CERN Document Server

    Li, Wai-Kee; Mak, Thomas Chung Wai; Mak, Kendrew Kin Wah

    2013-01-01

    This book consists of over 300 problems (and their solutions) in structural inorganic chemistry at the senior undergraduate and beginning graduate level. The topics covered comprise Atomic and Molecular Electronic States, Atomic Orbitals, Hybrid Orbitals, Molecular Symmetry, Molecular Geometry and Bonding, Crystal Field Theory, Molecular Orbital Theory, Vibrational Spectroscopy, and Crystal Structure. The central theme running through these topics is symmetry, molecular or crystalline. The problems collected in this volume originate in examination papers and take-home assignments that have been part of the teaching of the book's two senior authors' at The Chinese University of Hong Kong over the past four decades. The authors' courses include Chemical Bonding, Elementary Quantum Chemistry, Advanced Inorganic Chemistry, X-Ray Crystallography, etc. The problems have been tested by generations of students taking these courses.

  10. Fluorescent Properties of Manganese Halide Benzothiazole Inorganic-Organic Hybrids.

    Science.gov (United States)

    Yu, Hui; Mei, YingXuan; Wei, ZhenHong; Mei, GuangQuan; Cai, Hu

    2016-11-01

    The reaction of manganese (II) halides MnX2 and benzothiazole (btz) in the concentrated acids HX (X = Cl, Br) at 80 °C resulted in the formation of two inorganic-organic hybrid complexes: [(btz)2(MnX4)]·2H2O (X = Cl, 1; X = Br, 2). Both compounds showed green luminescence and exhibited moderate quantum yields of 43.17 % for 1 and 26.18 % for 2, which were directly originated from the tetrahedral coordination of Mn(2+) ion. Two organic - inorganic hybrids [(btz)2(MnX4)]·2H2O based on MnCl2, benzothiazole and halide acids emitted green light with the moderate quantum efficiencies when excited by 365 nm light. Graphical abstract Two organic-inorganic hybrids [(btz)2(MnX4)]·2H2O based on MnCl2, benzothiazole and halide acids emitted green light with the moderate quantum efficiencies when excited by 365 nm light.

  11. Metal-organic framework templated synthesis of porous inorganic materials as novel sorbents

    Energy Technology Data Exchange (ETDEWEB)

    Taylor-Pashow, Kathryn M. L.; Lin, Wenbin; Abney, Carter W.

    2017-03-21

    A novel metal-organic framework (MOF) templated process for the synthesis of highly porous inorganic sorbents for removing radionuclides, actinides, and heavy metals is disclosed. The highly porous nature of the MOFs leads to highly porous inorganic sorbents (such as oxides, phosphates, sulfides, etc) with accessible surface binding sites that are suitable for removing radionuclides from high level nuclear wastes, extracting uranium from acid mine drainage and seawater, and sequestering heavy metals from waste streams. In some cases, MOFs can be directly used for removing these metal ions as MOFs are converted to highly porous inorganic sorbents in situ.

  12. Inorganic Nanoparticle Nucleation on Polymer Matrices

    Science.gov (United States)

    Kosteleski, Adrian John

    The introduction of inorganic nanoparticles into organic materials enhances both the mechanical and chemical properties of the material. Metallic nanoparticles, like silver and gold, have been introduced into polymers for use as antimicrobial coatings or dielectric materials, respectively. The challenge in creating these materials currently is the difficulty to homogeneously disperse the particles throughout the polymer matrix. The uneven dispersion of nanoparticles can lead to less than optimal quality and undesired properties. By creating a polymer nanocomposite material with well-controlled size inorganic materials that are evenly dispersed throughout the polymer matrix; we can improve the materials performance and properties. The objective for this research is to use polymer networks for the in situ mineralization of silver and other metallic materials to create intricate inorganic structures. The work performed here studied the ability to nucleate silver nanoparticles using poly (acrylic acid) (PAA) as the templating agent. Ionic silver was chemically reduced by sodium borohydride (NaBH4) in the presence of PAA. The effect of varying reactant concentrations of silver, NaBH 4, and PAA on particle size was studied. Reaction conditions in terms of varying temperature and pH levels of the reaction solution were monitored to observe the effect of silver nanoparticle size, shape, and concentration. By monitoring the UV spectra over time the reaction mechanism of the silver reduction process was determined to be an autocatalytic process: a period of slow, continuous nucleation followed by rapid, autocatalytic growth. The reaction kinetics for this autocatalytic process is also reported. PAA was crosslinked both chemically and physically to 3 biopolymers; ELP, an elastin like peptide, cotton fabrics, and calcium alginate hydrogels. Various compositions of PAA were physically crosslinked with calcium alginate gels to design an antimicrobial hydrogel for use in wound

  13. Plasma chemistry for inorganic materials

    Science.gov (United States)

    Matsumoto, O.

    1980-01-01

    Practical application of plasma chemistry to the development of inorganic materials using both low temperature and warm plasmas are summarized. Topics cover: the surface nitrification and oxidation of metals; chemical vapor deposition; formation of minute oxide particles; the composition of oxides from chloride vapor; the composition of carbides and nitrides; freezing high temperature phases by plasma arc welding and plasma jet; use of plasma in the development of a substitute for petroleum; the production of silicon for use in solar cell batteries; and insulating the inner surface of nuclear fusion reactor walls.

  14. The inorganic constituents of echinoderms

    Science.gov (United States)

    Clarke, F.W.; Wheeler, W.C.

    1915-01-01

    In a recent paper on the composition of crinoid skeletons we showed that crinoids contain large quantities of magnesia, and that its proportion varies with the temperature of the water in which the creatures live. This result was so novel and surprising that it seemed desirable to examine other echinoderms and to ascertain whether they showed the same characteristics and regularity. A number of sea urchins and starfishes were therefore studied, their inorganic constituents being analyzed in the same manner as those of the crinoids

  15. The biological inorganic chemistry of zinc ions.

    Science.gov (United States)

    Krężel, Artur; Maret, Wolfgang

    2016-12-01

    The solution and complexation chemistry of zinc ions is the basis for zinc biology. In living organisms, zinc is redox-inert and has only one valence state: Zn(II). Its coordination environment in proteins is limited by oxygen, nitrogen, and sulfur donors from the side chains of a few amino acids. In an estimated 10% of all human proteins, zinc has a catalytic or structural function and remains bound during the lifetime of the protein. However, in other proteins zinc ions bind reversibly with dissociation and association rates commensurate with the requirements in regulation, transport, transfer, sensing, signalling, and storage. In contrast to the extensive knowledge about zinc proteins, the coordination chemistry of the "mobile" zinc ions in these processes, i.e. when not bound to proteins, is virtually unexplored and the mechanisms of ligand exchange are poorly understood. Knowledge of the biological inorganic chemistry of zinc ions is essential for understanding its cellular biology and for designing complexes that deliver zinc to proteins and chelating agents that remove zinc from proteins, for detecting zinc ion species by qualitative and quantitative analysis, and for proper planning and execution of experiments involving zinc ions and nanoparticles such as zinc oxide (ZnO). In most investigations, reference is made to zinc or Zn(2+) without full appreciation of how biological zinc ions are buffered and how the d-block cation Zn(2+) differs from s-block cations such as Ca(2+) with regard to significantly higher affinity for ligands, preference for the donor atoms of ligands, and coordination dynamics. Zinc needs to be tightly controlled. The interaction with low molecular weight ligands such as water and inorganic and organic anions is highly relevant to its biology but in contrast to its coordination in proteins has not been discussed in the biochemical literature. From the discussion in this article, it is becoming evident that zinc ion speciation is

  16. Anticorrosive organic/inorganic hybrid coatings

    Science.gov (United States)

    Gao, Tongzhai

    Organic/inorganic hybrid coating system was developed for anticorrosion applications using polyurea, polyurethane or epoxide as the organic phase and polysiloxane, formed by sol-gel process, as the inorganic phase. Polyurea/polysiloxane hybrid coatings were formulated and moisture cured using HDI isocyanurate, alkoxysilane-functionalized HDI isocyanurate, and tetraethyl orthosilicate (TEOS) oligomers. Two urethanes were prepared using the same components as abovementioned in addition to the oligoesters derived from either cyclohexane diacids (CHDA) and 2-butyl-2-ethyl-1,3-propanediol (BEPD) or adipic acid (AA), isophthalic acid (IPA), 1,6-hexanediol (HD), and trimethylol propane (TMP). Accelerated weathering and outdoor exposure were performed to study the weatherability of the polyurethane/polysiloxane hybrid coating system. FTIR and solid-state 13C NMR revealed that the degradation of the hybrid coatings occurred at the urethane and ester functionalities of the organic phase. DMA and DSC analyses showed the glass transition temperature increased and broadened after weathering. SEM was employed to observe the change of morphology of the hybrid coatings and correlated with the gloss variation after weathering. Rutile TiO2 was formulated into polyurethane/polysiloxane hybrid coatings in order to investigate the effect of pigmentation on the coating properties and the sol-gel precursor. Chemical interaction between the TiO2 and the sol-gel precursor was investigated using solid-state 29Si NMR and XPS. The morphology, mechanical, viscoelastic, thermal properties of the pigmented coatings were evaluated as a function of pigmentation volume concentration (PVC). Using AFM and SEM, the pigment were observed to be well dispersed in the polymer matrix. The thermal stability, the tensile modulus and strength of the coatings were enhanced with increasing PVC, whereas the pull-off adhesion and flexibility were reduced with increasing PVC. Finally, the pigmented coatings were

  17. Heterogeneous Catalysis of Polyoxometalate Based Organic–Inorganic Hybrids

    Directory of Open Access Journals (Sweden)

    Yuanhang Ren

    2015-03-01

    Full Text Available Organic–inorganic hybrid polyoxometalate (POM compounds are a subset of materials with unique structures and physical/chemical properties. The combination of metal-organic coordination complexes with classical POMs not only provides a powerful way to gain multifarious new compounds but also affords a new method to modify and functionalize POMs. In parallel with the many reports on the synthesis and structure of new hybrid POM compounds, the application of these compounds for heterogeneous catalysis has also attracted considerable attention. The hybrid POM compounds show noteworthy catalytic performance in acid, oxidation, and even in asymmetric catalytic reactions. This review summarizes the design and synthesis of organic–inorganic hybrid POM compounds and particularly highlights their recent progress in heterogeneous catalysis.

  18. Infrared Spectra of Simple Inorganic Ion Pairs in Solid Solution: A Physical Inorganic Chemistry Experiment.

    Science.gov (United States)

    Miller, Philip J.; Tong, William G.

    1980-01-01

    Presents a physical inorganic experiment in which large single crystals of the alkali halides doped with divalent ion impurities are prepared easily. Demonstrates the ion pairing of inorganic ions in solid solution. (CS)

  19. Identifying Affinity Classes of Inorganic Materials Binding Sequences via a Graph-Based Model.

    Science.gov (United States)

    Du, Nan; Knecht, Marc R; Swihart, Mark T; Tang, Zhenghua; Walsh, Tiffany R; Zhang, Aidong

    2015-01-01

    Rapid advances in bionanotechnology have recently generated growing interest in identifying peptides that bind to inorganic materials and classifying them based on their inorganic material affinities. However, there are some distinct characteristics of inorganic materials binding sequence data that limit the performance of many widely-used classification methods when applied to this problem. In this paper, we propose a novel framework to predict the affinity classes of peptide sequences with respect to an associated inorganic material. We first generate a large set of simulated peptide sequences based on an amino acid transition matrix tailored for the specific inorganic material. Then the probability of test sequences belonging to a specific affinity class is calculated by minimizing an objective function. In addition, the objective function is minimized through iterative propagation of probability estimates among sequences and sequence clusters. Results of computational experiments on two real inorganic material binding sequence data sets show that the proposed framework is highly effective for identifying the affinity classes of inorganic material binding sequences. Moreover, the experiments on the structural classification of proteins (SCOP) data set shows that the proposed framework is general and can be applied to traditional protein sequences.

  20. Inorganic and hybrid inorganic-organic systems for conservative treatments of stone and wood materials

    OpenAIRE

    Bergamonti, Laura

    2015-01-01

    Inorganic and hybrid inorganic-organic systems for conservative treatments of stone and wood materials The research has focused on the synthesis, characterization and application of inorganic and hybrid inorganic-organic systems for conservative treatments of stone and wood. The wood preservatives synthesized and tested for biocidal activity are polyamidoamines functionalized with hydroxyl and siloxane groups, while the coatings applied on the stones are water based TiO2 nanosols with ...

  1. Inorganic ion exchangers for nuclear waste remediation

    Energy Technology Data Exchange (ETDEWEB)

    Clearfield, A.; Bortun, A.; Bortun, L.; Behrens, E. [Texas A& M Univ., College Station, TX (United States)

    1997-10-01

    The objective of this work is to provide a broad spectrum of inorganic ion exchangers that can be used for a range of applications and separations involving remediation of groundwater and tank wastes. The authors intend to scale-up the most promising exchangers, through partnership with AlliedSignal Inc., to provide samples for testing at various DOE sites. While much of the focus is on exchangers for removal of Cs{sup +} and Sr{sup 2+} from highly alkaline tank wastes, especially at Hanford, the authors have also synthesized exchangers for acid wastes, alkaline wastes, groundwater, and mercury, cobalt, and chromium removal. These exchangers are now available for use at DOE sites. Many of the ion exchangers described here are new, and others are improved versions of previously known exchangers. They are generally one of three types: (1) layered compounds, (2) framework or tunnel compounds, and (3) amorphous exchangers in which a gel exchanger is used to bind a fine powder into a bead for column use. Most of these exchangers can be regenerated and used again.

  2. 29 CFR 1926.1118 - Inorganic arsenic.

    Science.gov (United States)

    2010-07-01

    ... 29 Labor 8 2010-07-01 2010-07-01 false Inorganic arsenic. 1926.1118 Section 1926.1118 Labor Regulations Relating to Labor (Continued) OCCUPATIONAL SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR... Inorganic arsenic. Note: The requirements applicable to construction work under this section are...

  3. 29 CFR 1915.1018 - Inorganic arsenic.

    Science.gov (United States)

    2010-07-01

    ... 29 Labor 7 2010-07-01 2010-07-01 false Inorganic arsenic. 1915.1018 Section 1915.1018 Labor Regulations Relating to Labor (Continued) OCCUPATIONAL SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR... § 1915.1018 Inorganic arsenic. Note: The requirements applicable to shipyard employment under...

  4. Inorganic materials synthesis in ionic liquids

    Directory of Open Access Journals (Sweden)

    Christoph Janiak

    2014-01-01

    Full Text Available The field of "inorganic materials from ionic liquids" (ILs is a young and dynamically growing research area for less than 10 years. The ionothermal synthesis in ILs is often connected with the preparation of nanomaterials, the use of microwave heating and in part also ultrasound. Inorganic material synthesis in ILs allows obtaining phases which are not accessible in conventional organic or aqueous solvents or with standard methods of solid-state chemistry or under such mild conditions. Cases at hand include "ligand-free" metal nanoparticles without added stabilizing capping ligands, inorganic or inorganic-organic hybrid solid-state compounds, large polyhedral clusters and exfoliated graphene from low-temperature synthesis. There are great expectations that ILs open routes towards new, possibly unknown, inorganic materials with advantageous properties that cannot (or only with great difficulty be made via conventional processes.

  5. On some problems of inorganic supramolecular chemistry.

    Science.gov (United States)

    Pervov, Vladislav S; Zotova, Anna E

    2013-12-02

    In this study, some features that distinguish inorganic supramolecular host-guest objects from traditional architectures are considered. Crystalline inorganic supramolecular structures are the basis for the development of new functional materials. Here, the possible changes in the mechanism of crystalline inorganic supramolecular structure self-organization at high interaction potentials are discussed. The cases of changes in the host structures and corresponding changes in the charge states under guest intercalation, as well as their impact on phase stability and stoichiometry are considered. It was demonstrated that the deviation from the geometrical and topological complementarity conditions may be due to the additional energy gain from forming inorganic supramolecular structures. It has been assumed that molecular recognition principles can be employed for the development of physicochemical analysis and interpretation of metastable states in inorganic crystalline alloys.

  6. Welcome to Inorganics: A New Open Access, Inclusive Forum for Inorganic Chemistry

    Directory of Open Access Journals (Sweden)

    Duncan H. Gregory

    2013-06-01

    Full Text Available One of the beauties of inorganic chemistry is its sheer diversity. Just as chemistry sits at the centre of the sciences, inorganic chemistry sits at the centre of chemistry itself. Inorganic chemists are fortunate in having the entire periodic table at their disposal, providing a palette for the creation of a multitude of rich and diverse compounds and materials from the simplest salts to the most complex of molecular species. It follows that the language of inorganic chemistry can thus be a demanding one, accommodating sub-disciplines with very different perspectives and frames of reference. One could argue that it is the unequivocal breadth of inorganic chemistry that empowers inorganic chemists to work at the interfaces, not just between the traditional Inorganic-Organic-Physical boundaries of the discipline, but in the regions where chemistry borders the other physical and life sciences, engineering and socio-economics. [...

  7. Synthesis and characterization of nanoscale magnetic drug-inorganic composites

    Institute of Scientific and Technical Information of China (English)

    SUN Hui; ZHANG Hui; David G. Evans; DUAN Xue

    2005-01-01

    The synthesis by direct coprecipitation and characterization of captopril (Cpl) and 5-aminosalicylic acid (5-ASA) intercalated ZnAl layered double hydroxides coated on MgFe2O4 magnetic core particles are reported. Powder XRD analysis shows the well-defined crystallite structure of the composites. TEM and XPS results reveal that a core-shell structure involving a drug-LDHs layer coated on MgFe2O4 particles is formed through Zn-O-Mg and/or Al-O-Mg linkages. VSM measurements demonstrate that the novel magnetic drug-inorganic composites possess considerable magnetization.

  8. Nanocomposites Derived from Polymers and Inorganic Nanoparticles

    Directory of Open Access Journals (Sweden)

    In-Yup Jeon

    2010-06-01

    Full Text Available Polymers are considered to be good hosting matrices for composite materials because they can easily be tailored to yield a variety of bulk physical properties. Moreover, organic polymers generally have long-term stability and good processability. Inorganic nanoparticles possess outstanding optical, catalytic, electronic and magnetic properties, which are significantly different their bulk states. By combining the attractive functionalities of both components, nanocomposites derived from organic polymers and inorganic nanoparticles are expected to display synergistically improved properties. The potential applications of the resultant nanocomposites are various, e.g. automotive, aerospace, opto-electronics, etc. Here, we review recent progress in polymer-based inorganic nanoparticle composites.

  9. Inorganic Nanoparticles Conjugated with Biofunctional Molecules

    Institute of Scientific and Technical Information of China (English)

    J.H.Choy

    2007-01-01

    1 Results We have attempted to conjugate inorganic nanoparticles with biofunctional molecules.Recently we were quite successful in demonstrating that a two-dimensional inorganic compound like layered double hydroxide (LDH),and natural and synthetic clays can be used as gene or drug delivery carriers1-4.To the best of our knowledge,such inorganic vectors are completely new and different from conventionally developed ones such as viruses and cationic liposomes,those which are limited in certain cases of ap...

  10. Inorganic biomaterials structure, properties and applications

    CERN Document Server

    Zhang, Xiang C

    2014-01-01

    This book provides a practical guide to the use and applications of inorganic biomaterials. It begins by introducing the concept of inorganic biomaterials, which includes bioceramics and bioglass. This concept is further extended to hybrid biomaterials consisting of inorganic and organic materials to mimic natural biomaterials. The book goes on to provide the reader with information on biocompatibility, bioactivity and bioresorbability. The concept of the latter is important because of the increasing role resorbable biomaterials are playing in implant applications. The book also introduces a n

  11. Inorganic chemically active adsorbents (ICAAs)

    Energy Technology Data Exchange (ETDEWEB)

    Ally, M.R. [Oak Ridge National Lab., TN (United States); Tavlarides, L.

    1997-10-01

    Oak Ridge National Laboratory (ORNL) researchers are developing a technology that combines metal chelation extraction technology and synthesis chemistry. They begin with a ceramic substrate such as alumina, titanium oxide or silica gel because they provide high surface area, high mechanical strength, and radiolytic stability. One preparation method involves silylation to hydrophobize the surface, followed by chemisorption of a suitable chelation agent using vapor deposition. Another route attaches newly designed chelating agents through covalent bonding by the use of coupling agents. These approaches provide stable and selective, inorganic chemically active adsorbents (ICAAs) tailored for removal of metals. The technology has the following advantages over ion exchange: (1) higher mechanical strength, (2) higher resistance to radiation fields, (3) higher selectivity for the desired metal ion, (4) no cation exchange, (5) reduced or no interference from accompanying anions, (6) faster kinetics, and (7) easy and selective regeneration. Target waste streams include metal-containing groundwater/process wastewater at ORNL`s Y-12 Plant (multiple metals), Savannah River Site (SRS), Rocky Flats (multiple metals), and Hanford; aqueous mixed wastes at Idaho National Engineering Laboratory (INEL); and scrubber water generated at SRS and INEL. Focus Areas that will benefit from this research include Mixed Waste, and Subsurface Contaminants.

  12. The quest for inorganic fullerenes

    Energy Technology Data Exchange (ETDEWEB)

    Pietsch, Susanne; Dollinger, Andreas; Strobel, Christoph H.; Ganteför, Gerd, E-mail: gerd.gantefoer@uni-konstanz.de, E-mail: ydkim91@skku.edu [Department of Physics, University of Konstanz, D-78457 Konstanz (Germany); Park, Eun Ji; Kim, Young Dok, E-mail: gerd.gantefoer@uni-konstanz.de, E-mail: ydkim91@skku.edu [Department of Chemistry, Sungkyunkwan University, 440-746 Suwon (Korea, Republic of); Seo, Hyun Ook [Center for Free-Electron Laser Science/DESY, D-22607 Hamburg (Germany); Idrobo, Juan-Carlos [Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 (United States); Pennycook, Stephen J. [Department of Materials Science and Engineering, National University of Singapore, Singapore 117575 (Singapore)

    2015-10-07

    Experimental results of the search for inorganic fullerenes are presented. Mo{sub n}S{sub m}{sup −} and W{sub n}S{sub m}{sup −} clusters are generated with a pulsed arc cluster ion source equipped with an annealing stage. This is known to enhance fullerene formation in the case of carbon. Analogous to carbon, the mass spectra of the metal chalcogenide clusters produced in this way exhibit a bimodal structure. The species in the first maximum at low mass are known to be platelets. Here, the structure of the species in the second maximum is studied by anion photoelectron spectroscopy, scanning transmission electron microscopy, and scanning tunneling microcopy. All experimental results indicate a two-dimensional structure of these species and disagree with a three-dimensional fullerene-like geometry. A possible explanation for this preference of two-dimensional structures is the ability of a two-element material to saturate the dangling bonds at the edges of a platelet by excess atoms of one element. A platelet consisting of a single element only cannot do this. Accordingly, graphite and boron might be the only materials forming nano-spheres because they are the only single element materials assuming two-dimensional structures.

  13. Sol-gel Process in Preparation of Organic-inorganic Hybrid Materials

    Directory of Open Access Journals (Sweden)

    Macan, J

    2008-07-01

    Full Text Available Organic-inorganic hybrid materials are a sort of nanostructured material in which the organic and inorganic phases are mixed at molecular level. The inorganic phase in hybrid materials is formed by the sol-gel process, which consists of reactions of hydrolysis and condensation of metal (usually silicon alkoxides. Flexibility of sol-gel process enables creation of hybrid materials with varying organic and inorganic phases in different ratios, and consequently fine-tuning of their properties. In order to obtain true hybrid materials, contact between the phases should be at molecular level, so phase separation between thermodynamically incompatible organic and inorganic phases has to be prevented. Phase interaction can be improved by formation of hydrogen or covalent bonds between them during preparation of hybrid materials. Covalent bond can be introduced by organically modified silicon alkoxides containing a reactive organic group (substituent capable of reacting with the organic phase. In order to obtain hybrid materials with desired structures, a detailed knowledge of hydrolysis and condensation mechanism is necessary. The choice of catalyst, whether acid or base, has the most significant influence on the structure of the inorganic phase. Other important parameters are alkoxide concentration, water: alkoxide ratio, type of alkoxide groups, solvent used, temperature, purity of chemicals used, etc. Hydrolysis and condensation of organically modified silicon alkoxides are additionally influenced by nature and size of the organic supstituent.

  14. 均匀设计法应用于NaZSM-5分子筛无机酸交换条件的优化%Optimization of inorganic acid exchange conditions of NaZSM-5 zeolite by uniform design

    Institute of Scientific and Technical Information of China (English)

    李光河; 叶晓雪; 刘杨青; 魏会娟; 苏慧; 王向宇

    2016-01-01

    采用无胺法水热合成NaZSM-5分子筛,分别用盐酸和硝酸将NaZSM-5分子筛交换为HZSM-5,考察酸浓度、交换时间及温度、液固比(V(交换液)∶m(催化剂))等对其催化环己烯水合制环己醇性能的影响。采用XRD、XRF、NH3-TPD、SEM和N2吸附-脱附等技术对试样进行表征。运用均匀设计法对分子筛无机酸交换条件进行优化。实验结果表明,无机酸交换方法较传统铵盐交换方法简便、节能和高效。最优盐酸交换条件为:盐酸浓度1.2 mol/L、交换温度80℃、交换时间3 h、液固比11 mL/g,环己醇理论收率为9.29%,实际收率为8.71%。最优硝酸交换条件为:硝酸浓度1.2 mol/L、交换温度63℃、交换时间3 h、液固比为11 mL/g,环己醇理论收率为8.92%,实际收率为8.90%。理论收率与实际收率较吻合,说明均匀设计法在分子筛无机酸交换条件优化上具有较高的实用价值。%NaZSM-5 zeolite was synthesized in an amine-free system by hydrothermal method, and HZSM-5 catalysts were prepared through the inorganic acid exchange of the NaZSM-5 zeolite with HCl and HNO3 separately. The effects of acid concentration,exchange time,exchange temperature and exchange liquid volume on the performances of the HZSM-5 catalysts in the hydration of cyclohexene to cyclohexanol were studied. The HZSM-5 catalysts were characterized by means of XRD,XRF,NH3-TPD,SEM and N2adsorption-desorption. The exchange conditions were optimized by means of uniform design. The results showed that the inorganic acid exchange method was simple,energy saving and high efficient compared with the traditional ammonium salt exchange method. Under the optimal HCl exchange conditions of HCl concentration of 1.2 mol/L,exchange temperature of 80℃,exchange time of 3 h and exchange liquid volume of 11 mL/g,the theoretical and actual yields of cyclohexanol were 9.29% and 8.71%,respectively. Under the optimal HNO3 exchange

  15. Structure of hybrid organic-inorganic sols for the preparation of hydrothermally stable membranes

    NARCIS (Netherlands)

    Castricum, H.L.; Sah, A.; Geenevasen, J.A.J.; Kreiter, R.; Blank, D.H.A.; Vente, J.F.; ten Elshof, J.E.

    2008-01-01

    A procedure for the preparation of hybrid sols for the synthesis of organic-inorganic microporous materials and thin film membranes is reported. We describe silane reactivity and sol structure for acid-catalysed colloidal sols from mixtures of either tetraethylorthosilicate (TEOS) and methyltriethox

  16. Inorganic nanoparticles for cancer imaging and therapy.

    Science.gov (United States)

    Huang, Huang-Chiao; Barua, Sutapa; Sharma, Gaurav; Dey, Sandwip K; Rege, Kaushal

    2011-11-07

    Inorganic nanoparticles have received increased attention in the recent past as potential diagnostic and therapeutic systems in the field of oncology. Inorganic nanoparticles have demonstrated successes in imaging and treatment of tumors both ex vivo and in vivo, with some promise towards clinical trials. This review primarily discusses progress in applications of inorganic nanoparticles for cancer imaging and treatment, with an emphasis on in vivo studies. Advances in the use of semiconductor fluorescent quantum dots, carbon nanotubes, gold nanoparticles (spheres, shells, rods, cages), iron oxide magnetic nanoparticles and ceramic nanoparticles in tumor targeting, imaging, photothermal therapy and drug delivery applications are discussed. Limitations and toxicity issues associated with inorganic nanoparticles in living organisms are also discussed.

  17. Inorganic arsenic poisoning in pastured feeder lambs

    Energy Technology Data Exchange (ETDEWEB)

    Nelson, H.A.; Crane, M.R.; Tomson, K.

    1971-01-01

    Clinical signs and necropsy findings in a group of feeder lambs were suggestive of inorganic arsenic poisoning. Source of exposure was established and toxic concentrations of arsenic were detected in the tissues. 13 references, 1 table.

  18. Determination of total arsenic, inorganic and organic arsenic species in wine.

    Science.gov (United States)

    Herce-Pagliai, C; Moreno, I; González, G; Repetto, M; Cameán, A M

    2002-06-01

    Forty-five wine samples from the south of Spain of different alcoholic strength were analysed for total arsenic and its inorganic [As(III), As(V)] and organic (monomethylarsonic acid [MMAA], dimethylarsinic acid [DMAA]) species. The As levels of the wine samples ranged from 2.1 to 14.6 microg l(-1). The possible effect of the alcoholic fermentation process on the levels of the total arsenic and arsenical species was studied. The average total arsenic levels for the different samples were very similar, without significant differences between all types of wines. In table wines and sherry, the percentages of total inorganic arsenic were 18.6 and 15.6%, with DMAA or MMAA being the predominant species, respectively. In most samples, DMAA was the most abundant species, but the total inorganic aresenic fraction was considerable, representing 25.4% of the total concentration of the element. The estimated daily intakes of total arsenic and total inorganic arsenic for average Spanish consumers were 0.78 and 0.15 microg/person day(-1), respectively. The results suggest that the consumption of these types of wines makes no significant contribution to the total and inorganic arsenic intake for normal drinkers. However, wine consumption contributes a higher arsenic intake than through consumption of beers and sherry brandies.

  19. Structure and properties of layered inorganic materials

    Institute of Scientific and Technical Information of China (English)

    Xue Duan

    2010-01-01

    @@ Inorganic layered materials are a class of advanced functional materials that have attracted considerable attention by virtue of their practical applications in a wide variety of fields. Sys-tematic studies of structure, design, synthesis, and fabrication processing may extend the range of practical utility of inor-ganic layered functional materials, in areas such as food industry,chemical industry, energy engineering, environmental engineer-ing, drug and gene delivery, electronics technology, and materials protection.

  20. Inorganic particle analysis of dental impression elastomers

    OpenAIRE

    Carlo,Hugo Lemes; FONSECA, Rodrigo Borges; Soares, Carlos José; Correr,Américo Bortolazzo; Correr-Sobrinho, Lourenço; Sinhoreti,Mário Alexandre Coelho

    2010-01-01

    The aim of this study was to determine quantitatively and qualitatively the inorganic particle fraction of commercially available dental elastomers. The inorganic volumetric fraction of two addition silicones (Reprosil Putty/Fluid and Flexitime Easy Putty/Fluid), three condensation silicones (Clonage Putty/Fluid, Optosil Confort/Xantopren VL and Silon APS Putty/Fluid), one polyether (Impregum Soft Light Body) and one polysulfide (Permlastic Light Body) was accessed by weighing a previously de...

  1. Inorganic nanolayers: structure, preparation, and biomedical applications

    Science.gov (United States)

    Saifullah, Bullo; Hussein, Mohd Zobir B

    2015-01-01

    Hydrotalcite-like compounds are two-dimensional inorganic nanolayers also known as clay minerals or anionic clays or layered double hydroxides/layered hydroxy salts, and have emerged as a single type of material with numerous biomedical applications, such as drug delivery, gene delivery, cosmetics, and biosensing. Inorganic nanolayers are promising materials due to their fascinating properties, such as ease of preparation, ability to intercalate different type of anions (inorganic, organic, biomolecules, and even genes), high thermal stability, delivery of intercalated anions in a sustained manner, high biocompatibility, and easy biodegradation. Inorganic nanolayers have been the focus for researchers over the last decade, resulting in widening application horizons, especially in the field of biomedical science. These nanolayers have been widely applied in drug and gene delivery. They have also been applied in biosensing technology, and most recently in bioimaging science. The suitability of inorganic nanolayers for application in drug delivery, gene delivery, biosensing technology, and bioimaging science makes them ideal materials to be applied for theranostic purposes. In this paper, we review the structure, methods of preparation, and latest advances made by inorganic nanolayers in such biomedical applications as drug delivery, gene delivery, biosensing, and bioimaging. PMID:26366081

  2. Inorganic nanolayers: structure, preparation, and biomedical applications.

    Science.gov (United States)

    Saifullah, Bullo; Hussein, Mohd Zobir B

    2015-01-01

    Hydrotalcite-like compounds are two-dimensional inorganic nanolayers also known as clay minerals or anionic clays or layered double hydroxides/layered hydroxy salts, and have emerged as a single type of material with numerous biomedical applications, such as drug delivery, gene delivery, cosmetics, and biosensing. Inorganic nanolayers are promising materials due to their fascinating properties, such as ease of preparation, ability to intercalate different type of anions (inorganic, organic, biomolecules, and even genes), high thermal stability, delivery of intercalated anions in a sustained manner, high biocompatibility, and easy biodegradation. Inorganic nanolayers have been the focus for researchers over the last decade, resulting in widening application horizons, especially in the field of biomedical science. These nanolayers have been widely applied in drug and gene delivery. They have also been applied in biosensing technology, and most recently in bioimaging science. The suitability of inorganic nanolayers for application in drug delivery, gene delivery, biosensing technology, and bioimaging science makes them ideal materials to be applied for theranostic purposes. In this paper, we review the structure, methods of preparation, and latest advances made by inorganic nanolayers in such biomedical applications as drug delivery, gene delivery, biosensing, and bioimaging.

  3. 21 CFR 862.1580 - Phosphorus (inorganic) test system.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Phosphorus (inorganic) test system. 862.1580... Systems § 862.1580 Phosphorus (inorganic) test system. (a) Identification. A phosphorus (inorganic) test system is a device intended to measure inorganic phosphorus in serum, plasma, and urine. Measurements...

  4. The ACS Inorganic Exam and Its Influence (?) on the Inorganic Curriculum.

    Science.gov (United States)

    Sienko, M. J.

    1980-01-01

    Summarizes results of a questionnaire asking if the ASC standarized test influences what is taught in inorganic chemistry courses. Chief controlling factors are indicated to be: (1) instructor's preference and (2) textbook content. Suggestions are given to enhance amount of inorganic chemistry in undergraduate curricula. (Author/JN)

  5. Foundation Coursework in Undergraduate Inorganic Chemistry: Results from a National Survey of Inorganic Chemistry Faculty

    Science.gov (United States)

    Raker, Jeffrey R.; Reisner, Barbara A.; Smith, Sheila R.; Stewart, Joanne L.; Crane, Johanna L.; Pesterfield, Les; Sobel, Sabrina G.

    2015-01-01

    A national survey of inorganic chemists explored the self-reported topics covered in foundation-level courses in inorganic chemistry at the postsecondary level; the American Chemical Society's Committee on Professional Training defines a foundation course as one at the conclusion of which, "a student should have mastered the vocabulary,…

  6. RIVERINE INORGANIC CARBON DYNAMICS: OVERVIEW AND PERSPECTIVE

    Institute of Scientific and Technical Information of China (English)

    YAO Guan-rong; GAO Quan-zhou

    2006-01-01

    Inorganic carbon, the great part of the riverine carbon exported to the ocean, plays an important role in the global carbon cycle and ultimately impacts the coupled carbon-climate system. An overview was made on both methods and results of the riverine inorganic carbon researches. In addition to routine in situ survey, measurement and calculation,the direct precipitation method and the gas evolution technique were commonly used to analyze dissolved inorganic carbon in natural water samples. Soil CO2, carbonate minerals and atmospheric CO2 incorporated into riverine inorganic carbon pool via different means, with bicarbonate ion being the dominant component. The concentration of inorganic carbon, the composition of carbon isotopes (δ13C and △14C), and their temporal or spatial variations in the streams were controlled by carbon input, output and changes of carbon biogeochemistry within the riverine system. More accurate flux estimation, better understanding of different influential processes, and quantitative determination of various inputs or outputs need to be well researched in future.

  7. Modeling the Thermodynamics of Mixed Organic-Inorganic Aerosols to Predict Water Activities and Phase Equilibria

    Science.gov (United States)

    Zuend, A.; Marcolli, C.; Luo, B.; Peter, T.

    2008-12-01

    Tropospheric aerosol particles contain mixtures of inorganic salts, acids, water, and a large variety of organic compounds. Interactions between these substances in liquid mixtures lead to discrepancies from ideal thermodynamic behavior. While the thermodynamics of aqueous inorganic systems at atmospheric temperatures are well established, little is known about the physicochemistry of mixed organic-inorganic particles. Salting-out and salting-in effects result from organic-inorganic interactions and are used to improve industrial separation processes. In the atmosphere, they may influence the aerosol phases. Liquid-liquid phase separations into a mainly polar (aqueous) and a less polar organic phase may considerably influence the gas/particle partitioning of semi-volatile substances compared to a single phase estimation. Moreover, the phases present in the aerosol define the reaction medium for heterogeneous and multiphase chemistry occurring in aerosol particles. A correct description of these phases is needed when gas- or cloud-phase reaction schemes are adapted to aerosols. Non-ideal thermodynamic behavior in mixtures is usually described by an expression for the excess Gibbs energy. We present the group-contribution model AIOMFAC (Aerosol Inorganic-Organic Mixtures Functional groups Activity Coefficients), which explicitly accounts for molecular interactions between solution constituents, both organic and inorganic, to calculate activities, chemical potentials and the total Gibbs energy of mixed systems. This model allows to compute vapor-liquid (VLE), liquid-liquid (LLE) and solid-liquid (SLE) equilibria within one framework. Focusing on atmospheric applications we considered eight different cations, five anions and a wide range of alcohols/polyols as organic compounds. With AIOMFAC, the activities of the components within an aqueous electrolyte solution are very well represented up to high ionic strength. We show that the semiempirical middle

  8. Leaching of DOC, DN, and inorganic constituents from scrap tires.

    Science.gov (United States)

    Selbes, Meric; Yilmaz, Ozge; Khan, Abdul A; Karanfil, Tanju

    2015-11-01

    One concern for recycle and reuse of scrap tires is the leaching of tire constituents (organic and inorganic) with time, and their subsequent potential harmful impacts in environment. The main objective of this study was to examine the leaching of dissolved organic carbon (DOC), dissolved nitrogen (DN), and selected inorganic constituents from scrap tires. Different sizes of tire chips and crumb rubber were exposed to leaching solutions with pH's ranging from 3.0 to 10.0 for 28days. The leaching of DOC and DN were found to be higher for smaller size tire chips; however, the leaching of inorganic constituents was independent of the size. In general, basic pH conditions increased the leaching of DOC and DN, whereas acidic pH conditions led to elevated concentrations of metals. Leaching was minimal around the neutral pH values for all the monitored parameters. Analysis of the leaching rates showed that components associated with the rubbery portion of the tires (DOC, DN, zinc, calcium, magnesium, etc.) exhibited an initial rapid followed by a slow release. On the other hand, a constant rate of leaching was observed for iron and manganese, which are attributed to the metal wires present inside the tires. Although the total amounts that leached varied, the observed leaching rates were similar for all tire chip sizes and leaching solutions. Operation under neutral pH conditions, use of larger size tire chips, prewashing of tires, and removal of metal wires prior to application will reduce the impact of tire recycle and reuse.

  9. Degradation of methyl and ethyl mercury into inorganic mercury by hydroxyl radical produced from rat liver microsomes

    Energy Technology Data Exchange (ETDEWEB)

    Suda, Ikuo (Kumamoto Univ. (Japan). Dept. of Pharmacology); Hirayama, Kimiko (Kumamoto Univ. (Japan). Coll. of Medical Science)

    1992-07-01

    Liver microsomes were prepared from Wistar rat by the Ca{sup 2+} aggregation method. Under various conditions, ethyl mercury chloride (EtHgCl) or methyl mercury chloride (MeHgCl) was incubated with the microsomal preparations. After the incubation, the amounts of inorganic Hg and hydroxyl radical (.OH) in the preparations were determined. Although the preparations alone produced a small amount of inorganic Hg and .OH, the addition of NADPH to the preparations increased both inorganic Hg and .OH production, which were further accelerated by the addition of KCN. The addition of Fe(III)EDTA, a .OH formation promoter, to the microsome-NADPH-KCN system increased inorganic Hg production, whereas the addition of diethylenetriamine pentaacetic acid, a .OH formation inhibitor, decreased inorganic Hg production. When .OH scavengers such as mannitol and dimethyl sulfoxide were added to this system, the inorganic Hg production decreased. These results suggested that the .OH produced from liver microsomes was responsible for the degradation of MeHg and EtHg. Since both .OH and inorganic Hg production decreased with a concomitant decrease in NADPH-cytochrome P-450 reductase activities, it is suggested that this enzyme may be involved in the microsomal degradation of MeHg and EtHg. (orig.).

  10. 46 CFR 151.50-20 - Inorganic acids.

    Science.gov (United States)

    2010-10-01

    ... a head of water at least 8 feet above the tank top or the highest level the lading may rise... described in § 151.03-25. No shutoff valve or frangible disk shall be fitted in the vent lines. (b)(1... pounds per square inch gauge. Hydrochloric Acid—50 pounds per square inch gauge. Hydrofluorosilicic...

  11. Inorganic Nanoparticles for Multimodal Molecular Imaging

    Directory of Open Access Journals (Sweden)

    Magdalena Swierczewska

    2011-01-01

    Full Text Available Multimodal molecular imaging can offer a synergistic improvement of diagnostic ability over a single imaging modality. Recent development of hybrid imaging systems has profoundly impacted the pool of available multimodal imaging probes. In particular, much interest has been focused on biocompatible, inorganic nanoparticle-based multimodal probes. Inorganic nanoparticles offer exceptional advantages to the field of multimodal imaging owing to their unique characteristics, such as nanometer dimensions, tunable imaging properties, and multifunctionality. Nanoparticles mainly based on iron oxide, quantum dots, gold, and silica have been applied to various imaging modalities to characterize and image specific biologic processes on a molecular level. A combination of nanoparticles and other materials such as biomolecules, polymers, and radiometals continue to increase functionality for in vivo multimodal imaging and therapeutic agents. In this review, we discuss the unique concepts, characteristics, and applications of the various multimodal imaging probes based on inorganic nanoparticles.

  12. Microporous Inorganic Membranes as Proton Exchange Membranes

    Energy Technology Data Exchange (ETDEWEB)

    Vichi, F.M. Tejedor-Tejedor, M.I. Anderson, Marc A

    2002-08-28

    Porous oxide electrolyte membranes provide an alternative approach to fabricating proton exchange membrane fuel cells based on inorganic materials. This study focused on elucidating the properties of these inorganic membranes that make them good electrolyte materials in membrane electrode assemblies; in particular, we investigated several properties that affect the nature of proton conductivity in these membranes. This report discusses our findings on the effect of variables such as site density, amount of surface protonation and surface modification on the proton conductivity of membranes with a fixed pore structure under selected conditions. Proton conductivities of these inorganic membranes are similar to conductivities of nafion, the polymeric membrane most commonly used in low temperature fuel cells.

  13. Inorganic nanocarriers for platinum drug delivery

    Directory of Open Access Journals (Sweden)

    Ping’an Ma

    2015-12-01

    Full Text Available Nowadays platinum drugs take up almost 50% of all the clinically used anticancer drugs. Besides cisplatin, novel platinum agents including sterically hindered platinum (II drugs, chemically reductive platinum (IV drugs, photosensitive platinum (IV drugs, and multinuclear platinum drugs have been developed recently, with a few entering clinic trials. Rapid development of nanobiotechnology makes targeted delivery of anticancer platinum agents to the tumor site possible, while simultaneously minimizing toxicity and maximizing the drug efficacy. Being versatile drug carriers to deliver platinum drugs, inorganic nanovehicles such as gold nanoparticles, iron oxide nanomaterials, carbon nanotubes, mesoporous nanosilica, metal-organic frameworks (MOFs, have been extensively studied over the past decades. In contrast to conventional polymeric and lipid nanoparticles, inorganic nanoparticles based drug carriers are peculiar as they have shown excellent theranostic effects, revealing themselves an indispensable part of future nanomedicine. Here, we will elaborate recent research advances on fabrication of inorganic nanoparticles for platinum drug delivery.

  14. Biotransformation of inorganic arsenic in a marine herbivorous fish Siganus fuscescens after dietborne exposure.

    Science.gov (United States)

    Zhang, Wei; Chen, Lizhao; Zhou, Yanyan; Wu, Yun; Zhang, Li

    2016-03-01

    Arsenic (As) is well known to be biodiminished along marine food chains. The marine herbivorous fish at a lower trophic level are expected to accumulate more As. However, little is known about how marine herbivorous fish biotransform the potential high As bioaccumulation. Therefore, the present study quantified the biotransformation of two inorganic As species (As(III) and As(V)) in a marine herbivorous fish Siganus fuscescens following dietborne exposure. The fish were fed on As contaminated artificial diets at nominal concentrations of 400 and 1500 μg As(III) or As(V) g(-1) (dry weight) for 21 d and 42 d. After exposure, As concentrations in intestine, liver, and muscle tissues of rabbitfish increased significantly and were proportional to the inorganic As exposure concentrations. The present study demonstrated that both inorganic As(III) and As(V) in the dietborne phases were able to be biotransformed to the less toxic arsenobetaine (AsB) (63.3-91.3% in liver; 79.0%-95.2% in muscle). The processes of As biotransformation in rabbitfish could include oxidation of As(III) to As(V), reduction of As(V) to As(III), methylation to monomethylarsonic acid (MMA) and dimethylarsinic acid (DMA), and subsequent conversion to AsB. These results also demonstrated that AsB synthesis processes were diverse facing different inorganic As species in different tissues. In summary, the present study elucidated that marine herbivorous fish had high ability to biotransform inorganic As to the organic forms (mainly AsB), resulting in high As bioaccumulation. Therefore, marine herbivorous fish could detoxify inorganic As in the natural environment.

  15. Plant uptake of dual-labeled organic N biased by inorganic C uptake

    DEFF Research Database (Denmark)

    Rasmussen, Jim; Sauheitl, Leopold; Eriksen, Jørgen;

    2010-01-01

    Direct plant uptake of organic nitrogen (N) is often studied using the dual-labeling approach (15N + 13C or 15N + 14C). However, the method might be hampered by uptake of labeled inorganic carbon (C) produced by mineralization of labeled organic compounds. Here we report the results from a triple...... glycine or CO2-3 , but found no differences in uptake rates between these C-sources. The uptake of inorganic C to the shoot tissue was higher for maize grown in full light compared to shading, which indicates a passive uptake of inorganic C with water. We conclude that uptake of inorganic C produced...... labeling experiment (15N + 13C + 14C) investigating whether root uptake of labeled inorganic C can bias the results obtained in studies of organic N uptake using dual-labeled amino acids (15N, 13C). In a rhizosphere tube experiment we investigated 13C and 14C uptake by maize either supplied with labeled...

  16. Inorganic Reactive Sulfur-Nitrogen Species: Intricate Release Mechanisms or Cacophony in Yellow, Blue and Red?

    Science.gov (United States)

    Grman, Marian; Nasim, Muhammad Jawad; Leontiev, Roman; Misak, Anton; Jakusova, Veronika; Ondrias, Karol; Jacob, Claus

    2017-02-15

    Since the heydays of Reactive Sulfur Species (RSS) research during the first decade of the Millennium, numerous sulfur species involved in cellular regulation and signalling have been discovered. Yet despite the general predominance of organic species in organisms, recent years have also seen the emergence of inorganic reactive sulfur species, ranging from inorganic polysulfides (HSx(-)/Sx(2-)) to thionitrous acid (HSNO) and nitrosopersulfide (SSNO(-)). These inorganic species engage in a complex interplay of reactions in vitro and possibly also in vivo. Employing a combination of spectrophotometry and sulfide assays, we have investigated the role of polysulfanes from garlic during the release of nitric oxide ((•)NO) from S-nitrosoglutathione (GSNO) in the absence and presence of thiol reducing agents. Our studies reveal a distinct enhancement of GSNO decomposition by compounds such as diallyltrisulfane, which is most pronounced in the presence of cysteine and glutathione and presumably proceeds via the initial release of an inorganic mono- or polysulfides, i.e., hydrogen sulfide (H₂S) or HSx(-), from the organic polysulfane. Albeit being of a preliminary nature, our spectrophotometric data also reveals a complicated underlying mechanism which appears to involve transient species such as SSNO(-). Eventually, more in depth studies are required to further explore the underlying chemistry and wider biological and nutritional implications of this interplay between edible garlic compounds, reductive activation, inorganic polysulfides and their interplay with (•)NO storage and release.

  17. Inorganic Reactive Sulfur-Nitrogen Species: Intricate Release Mechanisms or Cacophony in Yellow, Blue and Red?

    Directory of Open Access Journals (Sweden)

    Marian Grman

    2017-02-01

    Full Text Available Since the heydays of Reactive Sulfur Species (RSS research during the first decade of the Millennium, numerous sulfur species involved in cellular regulation and signalling have been discovered. Yet despite the general predominance of organic species in organisms, recent years have also seen the emergence of inorganic reactive sulfur species, ranging from inorganic polysulfides (HSx−/Sx2− to thionitrous acid (HSNO and nitrosopersulfide (SSNO−. These inorganic species engage in a complex interplay of reactions in vitro and possibly also in vivo. Employing a combination of spectrophotometry and sulfide assays, we have investigated the role of polysulfanes from garlic during the release of nitric oxide (•NO from S-nitrosoglutathione (GSNO in the absence and presence of thiol reducing agents. Our studies reveal a distinct enhancement of GSNO decomposition by compounds such as diallyltrisulfane, which is most pronounced in the presence of cysteine and glutathione and presumably proceeds via the initial release of an inorganic mono- or polysulfides, i.e., hydrogen sulfide (H2S or HSx−, from the organic polysulfane. Albeit being of a preliminary nature, our spectrophotometric data also reveals a complicated underlying mechanism which appears to involve transient species such as SSNO−. Eventually, more in depth studies are required to further explore the underlying chemistry and wider biological and nutritional implications of this interplay between edible garlic compounds, reductive activation, inorganic polysulfides and their interplay with •NO storage and release.

  18. Modelling iodide – iodate speciation in atmospheric aerosol: Contributions of inorganic and organic iodine chemistry

    Directory of Open Access Journals (Sweden)

    S. Pechtl

    2007-01-01

    Full Text Available The speciation of iodine in atmospheric aerosol is currently poorly understood. Models predict negligible iodide concentrations but accumulation of iodate in aerosol, both of which is not confirmed by recent measurements. We present an updated aqueous phase iodine chemistry scheme for use in atmospheric chemistry models and discuss sensitivity studies with the marine boundary layer model MISTRA. These studies show that iodate can be reduced in acidic aerosol by inorganic reactions, i.e., iodate does not necessarily accumulate in particles. Furthermore, the transformation of particulate iodide to volatile iodine species likely has been overestimated in previous model studies due to negligence of collision-induced upper limits for the reaction rates. However, inorganic reaction cycles still do not seem to be sufficient to reproduce the observed range of iodide – iodate speciation in atmospheric aerosol. Therefore, we also investigate the effects of the recently suggested reaction of HOI with dissolved organic matter to produce iodide. If this reaction is fast enough to compete with the inorganic mechanism, it would not only directly lead to enhanced iodide concentrations but, indirectly via speed-up of the inorganic iodate reduction cycles, also to a decrease in iodate concentrations. Hence, according to our model studies, organic iodine chemistry, combined with inorganic reaction cycles, is able to reproduce observations. The presented chemistry cycles are highly dependent on pH and thus offer an explanation for the large observed variability of the iodide – iodate speciation in atmospheric aerosol.

  19. A novel speciation alternative for the determination of inorganic arsenic in marine samples

    DEFF Research Database (Denmark)

    Rasmussen, Rie Romme; Hedegaard, Rikke Susanne Vingborg; Herbst, M. Birgitte Koch

    Arsenic (As) is bioaccumulated from seawater to concentrations in the mg/kg range in marine animals. More than 50 naturally-occurring arsenic containing species, both inorganic and organic forms, have been identified in marine animals. The organic forms are mainly considered to be non-toxic, wher......Arsenic (As) is bioaccumulated from seawater to concentrations in the mg/kg range in marine animals. More than 50 naturally-occurring arsenic containing species, both inorganic and organic forms, have been identified in marine animals. The organic forms are mainly considered to be non...... of inorganic arsenic in marine based food is based on microwave extraction, species separation by strong anion solid phase extraction (SPE) and hydride generation atomic absorption spectrometry (HG-AAS) detection. Separation organic arsenic compounds (e.g. MA, DMA and AB) and inorganic arsenic in the form...... conditions. In brief: The sample is heated with a hydrochloric acid and hydrogen peroxide solution (20 minutes at 90 °C with 0.06 M HCl, 3 % H2O2). Hereby the sample is solubilised and As(III) is oxidised to As(V). Inorganic arsenic is selectively separated from other arsenic compounds using strong anion...

  20. Engineered inorganic core/shell nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Mélinon, Patrice, E-mail: patrice.melinon@univ-lyon1.fr [Institut Lumière matière Université Claude Bernard Lyon 1 et CNRS et OMNT, Domaine Scientifique de la Doua, Bâtiment Léon Brillouin, 43 Boulevard du 11 Novembre 1918, F 69622 Villeurbanne (France); Begin-Colin, Sylvie [IPCMS et OMNT, 23 rue du Loess BP 43, 67034 STRASBOURG Cedex 2 (France); Duvail, Jean Luc [IMN UMR 6502 et OMNT Campus Sciences : 2 rue de la Houssinire, BP32229, 44322 Nantes Cedex3 (France); Gauffre, Fabienne [SPM et OMNT : Institut des sciences chimiques de Rennes - UMR 6226, 263 Avenue du General Leclerc, CS 74205, 35042 RENNES Cedex (France); Boime, Nathalie Herlin [IRAMIS-NIMBE, Laboratoire Francis Perrin (CEA CNRS URA 2453) et OMNT, Bat 522, CEA Saclay, 91191 Gif sur Yvette Cedex (France); Ledoux, Gilles [Institut Lumière Matière Université Claude Bernard Lyon 1 et CNRS et OMNT, Domaine Scientifique de la Doua, Bâtiment Alfred Kastler 43 Boulevard du 11 Novembre 1918 F 69622 Villeurbanne (France); Plain, Jérôme [Universit de technologie de Troyes LNIO-ICD, CNRS et OMNT 12 rue Marie Curie - CS 42060 - 10004 Troyes cedex (France); Reiss, Peter [CEA Grenoble, INAC-SPrAM, UMR 5819 CEA-CNRS-UJF et OMNT, Grenoble cedex 9 (France); Silly, Fabien [CEA, IRAMIS, SPEC, TITANS, CNRS 2464 et OMNT, F-91191 Gif sur Yvette (France); Warot-Fonrose, Bénédicte [CEMES-CNRS, Université de Toulouse et OMNT, 29 rue Jeanne Marvig F 31055 Toulouse (France)

    2014-10-20

    It has been for a long time recognized that nanoparticles are of great scientific interest as they are effectively a bridge between bulk materials and atomic structures. At first, size effects occurring in single elements have been studied. More recently, progress in chemical and physical synthesis routes permitted the preparation of more complex structures. Such structures take advantages of new adjustable parameters including stoichiometry, chemical ordering, shape and segregation opening new fields with tailored materials for biology, mechanics, optics magnetism, chemistry catalysis, solar cells and microelectronics. Among them, core/shell structures are a particular class of nanoparticles made with an inorganic core and one or several inorganic shell layer(s). In earlier work, the shell was merely used as a protective coating for the core. More recently, it has been shown that it is possible to tune the physical properties in a larger range than that of each material taken separately. The goal of the present review is to discuss the basic properties of the different types of core/shell nanoparticles including a large variety of heterostructures. We restrict ourselves on all inorganic (on inorganic/inorganic) core/shell structures. In the light of recent developments, the applications of inorganic core/shell particles are found in many fields including biology, chemistry, physics and engineering. In addition to a representative overview of the properties, general concepts based on solid state physics are considered for material selection and for identifying criteria linking the core/shell structure and its resulting properties. Chemical and physical routes for the synthesis and specific methods for the study of core/shell nanoparticle are briefly discussed.

  1. Interconnection of nanoparticles within 2D superlattices of PbS/oleic acid thin films.

    Science.gov (United States)

    Simon, Paul; Bahrig, Lydia; Baburin, Igor A; Formanek, Petr; Röder, Falk; Sickmann, Jan; Hickey, Stephen G; Eychmüller, Alexander; Lichte, Hannes; Kniep, Rüdiger; Rosseeva, Elena

    2014-05-21

    Make it connected! 2D close-packed layers of inorganic nanoparticles are interconnected by organic fibrils of oleic acid as clearly visualized by electron holography. These fibrils can be mineralised by PbS to transform an organic-inorganic framework to a completely interconnected inorganic semiconducting 2D array.

  2. 29 CFR 1910.1018 - Inorganic arsenic.

    Science.gov (United States)

    2010-07-01

    ...) Engineering plans and studies used to determine methods selected for controlling exposure to inorganic arsenic... such exposures. The following three sections quoted from “Occupational Diseases: A Guide to Their.... Arsenic; chronic human intoxication. J. Occup. Med. 2:137. Elkins, H. B. 1959. The Chemistry of...

  3. The influence of various inorganic acids on the adsorption performance of the polypyrrole/TiO2 composites%不同无机酸对聚吡咯/TiO2复合物的吸附性能影响

    Institute of Scientific and Technical Information of China (English)

    冯江涛; 李晶晶; 徐浩; 延卫

    2016-01-01

    考察了不同无机酸对PPy/TiO2复合物吸附性能的影响。首先分别在 HNO3、H2 SO4和 H3 PO4体系中合成了聚吡咯(PPy)/TiO2复合物(分别简写为 N-PPy/TiO2、S-PPy/TiO2和P-PPy/TiO2)。以红外光谱、热重分析、Zeta电位、比表面积分析和扫描电镜等测试方法对复合物的物理化学性能进行了表征。接着以几种合成的复合对阴离子染料酸性红 G和阳离子染料亚甲基蓝进行吸附研究,发现无机酸对合成的复合物的吸附性有较大的影响。几种复合物均可在30min 内达到吸附平衡,并且可以重复使用6次以上吸附量没有明显的降低。其中S-PPy/TiO2的吸附性能最好,其对 ARG和 MB的最大吸附量分别达到218.34mg/g 和314.68mg/g。复合物对染料的吸附过程符合准二级动力学模型和 Langmuir 吸附等温式。对 S-PPy/TiO2进行吸附热力学研究表明,其对染料的吸附过程为熵增的自发过程。%This study focused on the impact of various inorganic acids on the adsorption polypyrrole/TiO2 (PPy/TiO2 )composites.Firstly,PPy/TiO2 composites were prepared in the HNO3 (N-PPy/TiO2 )、H2SO4 (S-PPy/TiO2 )and H3PO4 (P-PPy/TiO2 )systems,respectively. FT-IR spectra, TG analysis, Zeta potential, specific surface area analysis and SEM were employed to character the physicochemical properties of the composites.Secondly,the adsorption of the as-prepared composites for anionic dye Acid red G (ARG)and cationic dye methylene blue (MB)were investigated.It was found that the adsorption performance of the composites prepared in acid system has been greatly improved.The adsorption equilibrium of all composites can reach in 30min.The composites could be reused for 6 cycles without obvious loss of adsorption capacity.S-PPy/TiO2 composite had the best adsorption properties.Its maximum adsorption capacity for ARG and MB were 218.34 and 314.68mg/g,respectively.The adsorption process of dyes onto the composites was in accordance with

  4. Thermoplastic Polymer Nanocomposites Based on Inorganic Fullerene-like Nanoparticles and Inorganic Nanotubes

    Directory of Open Access Journals (Sweden)

    Mohammed Naffakh

    2014-06-01

    Full Text Available Using inorganic fullerene-like (IF nanoparticles and inorganic nanotubes (INT in organic-inorganic hybrid composite, materials provide the potential for improving thermal, mechanical, and tribological properties of conventional composites. The processing of such high-performance hybrid thermoplastic polymer nanocomposites is achieved via melt-blending without the aid of any modifier or compatibilizing agent. The incorporation of small quantities (0.1–4 wt.% of IF/INTs (tungsten disulfide, IF-WS2 or molybdenum disulfide, MoS2 generates notable performance enhancements through reinforcement effects and excellent lubricating ability in comparison with promising carbon nanotubes or other inorganic nanoscale fillers. It was shown that these IF/INT nanocomposites can provide an effective balance between performance, cost effectiveness, and processability, which is of significant importance for extending the practical applications of diverse hierarchical thermoplastic-based composites.

  5. Preparation, Properties and Application of Polymeric Organic-Inorganic Nanocomposites

    Institute of Scientific and Technical Information of China (English)

    任杰; 刘艳; 唐小真

    2003-01-01

    Six preparation methods for polymeric organic-inorganic nanocomposites and their respective mechanisms and features are reviewed. The extraordinary properties of polymeric organic-inorganic nanocomposites are discussed,and their potential applications are evaluated.

  6. Inorganic Nitrogen Wet Deposition for the Conterminous United States, 1984

    Data.gov (United States)

    U.S. Geological Survey, Department of the Interior — Annual inorganic nitrogen wet deposition were estimated for the conterminous United States for 1984. The estimates were derived from inorganic nitrogen...

  7. Inorganic Nitrogen Wet Deposition for the Conterminous United States, 1962

    Data.gov (United States)

    U.S. Geological Survey, Department of the Interior — Annual inorganic nitrogen wet deposition were estimated for the conterminous United States for 1962. The estimates were derived from inorganic nitrogen...

  8. Inorganic Nitrogen Wet Deposition for the Conterminous United States, 1983

    Data.gov (United States)

    U.S. Geological Survey, Department of the Interior — Annual inorganic nitrogen wet deposition were estimated for the conterminous United States for 1983. The estimates were derived from inorganic nitrogen...

  9. Inorganic Nitrogen Wet Deposition for the Conterminous United States, 1964

    Data.gov (United States)

    U.S. Geological Survey, Department of the Interior — Annual inorganic nitrogen wet deposition were estimated for the conterminous United States for 1964. The estimates were derived from inorganic nitrogen...

  10. Striking a Balance: Experiment and Concept in Undergraduate Inorganic Chemistry.

    Science.gov (United States)

    Frey, John E.

    1990-01-01

    Described is an inorganic chemistry course based on the premise that a balanced understanding of inorganic chemistry requires knowledge of the experimental, theoretical, and technological aspects of the subject. A detailed description of lectures and laboratories is included. (KR)

  11. Relation of dietary inorganic arsenic exposure and urinary inorganic arsenic metabolites excretion in Japanese subjects.

    Science.gov (United States)

    Oguri, Tomoko; Yoshinaga, Jun; Suzuki, Yayoi; Tao, Hiroaki; Nakazato, Tetsuya

    2017-03-08

    Inorganic arsenic (InAs) is a ubiquitous metalloid that has been shown to exert multiple adverse health outcomes. Urinary InAs and its metabolite concentration has been used as a biomarker of arsenic (As) exposure in some epidemiological studies, however, quantitative relationship between daily InAs exposure and urinary InAs metabolites concentration has not been well characterized. We collected a set of 24-h duplicated diet and spot urine sample of the next morning of diet sampling from 20 male and 19 female subjects in Japan from August 2011 to October 2012. Concentrations of As species in duplicated diet and urine samples were determined by using liquid chromatography-ICP mass spectrometry with a hydride generation system. Sum of the concentrations of urinary InAs and methylarsonic acid (MMA) was used as a measure of InAs exposure. Daily dietary InAs exposure was estimated to be 0.087 µg kg(-1) day(-1) (Geometric mean, GM), and GM of urinary InAs+MMA concentrations was 3.5 ng mL(-1). Analysis of covariance did not find gender-difference in regression coefficients as significant (P > 0.05). Regression equation Log 10 [urinary InAs+MMA concentration] = 0.570× Log 10 [dietary InAs exposure level per body weight] + 1.15 was obtained for whole data set. This equation would be valuable in converting urinary InAs concentration to daily InAs exposure, which will be important information in risk assessment.

  12. A study on major inorganic ion composition of atmospheric aerosols.

    Science.gov (United States)

    Salve, P R; Krupadam, R J; Wate, S R

    2007-04-01

    Atmospheric aerosol samples were collected from Akola and Buldana region covering around 40 sqkm area during October-November 2002 and were analyzed for ten major inorganic ions namely F-, Cl-, NO3-, SO4(2-), PO4(2-), Na+, K+, Ca2+, Mg2+ and NH4+ using ion chromatographic technique. The average mass of aerosols was found to be 225.81 microg/m3 with standard deviation of 31.29 and average total water soluble load of total cations and anions was found to be 4.32 microg/m3. The concentration of ions in samples showed a general pattern as SO4(2-) > NO3- > Cl- > PO4(2-) > F- for anions and Na+ > Ca2+ > NH4+ > Mg2+ > K+ for cations. The overall composition of the aerosols was taken into account to identify the sources. The trend showed higher concentration of sodium followed by calcium, sulfate, nitrate, phosphate and ammoinum and found to be influenced by terrestrial sources. The presence of SO4(2-) and NO3- in aerosols may be due to re-suspension of soil particles. Ca2+, Mg2+ and Cl- are to be derived from soil materials. The presence of NH4+ may be attributed to the reaction of NH3 vapors with acidic gases may react or condense on an acidic particle surface of anthropogenic origin. The atmospheric aerosol is slightly acidic due to neutralization of basicity by SO2 and NO(x).

  13. UV-C photolysis of endocrine disruptors. The influence of inorganic peroxides

    Energy Technology Data Exchange (ETDEWEB)

    Rivas, Javier, E-mail: fjrivas@unex.es [Departamento de Ingenieria Quimica y Quimica Fisica, Facultad de Ciencias, Avenida de Elvas S/N, 06071 Badajoz (Spain); Gimeno, Olga; Borralho, Teresa; Carbajo, Maria [Departamento de Ingenieria Quimica y Quimica Fisica, Facultad de Ciencias, Avenida de Elvas S/N, 06071 Badajoz (Spain)

    2010-02-15

    Norfloxacin, doxycycline and mefenamic acid have been photolysed with UV-C radiation (254 nm) in the presence and absence of inorganic peroxides (hydrogen peroxide or sodium monopersulfate). Quantum yields in the range (1.1-4.5) x 10{sup -3} mol Einstein{sup -1} indicate the low photo-reactivity of these pharmaceuticals. Inorganic peroxides considerably enhanced the contaminants conversion, although no appreciable mineralization could be obtained. A simplistic reaction mechanism for the hydrogen peroxide promoted experiments allowed for a rough estimation of the rate constant between hydroxyl radicals and norfloxacin (k > 1 x 10{sup 9} M{sup -1} s{sup -1}), doxycycline (k > 1.5 x 10{sup 9} M{sup -1} s{sup -1}) and mefenamic acid (k > 11.0 x 10{sup 9} M{sup -1} s{sup -1}).

  14. Organic and inorganic inputs and losses in an irrigated corn field after inorganic fertilizer or manure application

    Science.gov (United States)

    Little is known about inorganic fertilizer or manure effects on organic carbon (OC) and inorganic C (IC) losses from a furrow irrigated field, particularly in the context of other system C gains or losses. In 2003 and 2004, we measured dissolved organic and inorganic C (DOC, DIC), particulate OC an...

  15. Tuning the Mechanical Properties of Tapioca Starch by Plasticizers, Inorganic Fillers and Agrowaste-Based Fillers

    OpenAIRE

    Edwin Azwar; Minna Hakkarainen

    2012-01-01

    Mechanical properties of tapioca starch-based films were tuned by different additives and additive combinations. The additives included plasticizers (glycerol, sorbitol, and citric acid), inorganic fillers (halloysite and kaolin), and agrowaste-based fillers (milled wood flour and rice bran). In addition, new biobased additives were prepared from wood flour and rice bran through liquefaction reaction. Through different additive combinations, starch-based materials with significant differences...

  16. Evidence of inorganic chlorine gases other than hydrogen chloride in marine surface air

    OpenAIRE

    Pszenny, A. A. P.; W. C. Keene; Jacob, Daniel James; S. Fan; J. R. Maben; Zetwo, M. P.; Springer-Young, M.; J. N. Galloway

    1993-01-01

    We report the first measurements of inorganic chlorine gases in the marine atmosphere using a new tandem mist chamber method. Surface air was sampled during four days including one diel cycle in January, 1992, at Virginia Key, Florida. Concentrations of HCl* (including HCl, ClNO3, ClNO2, and NOCl) were in the range 40 to 268 pptv and concentrations of Cl2* (including Cl2 and any HOCl not trapped in the acidic mist chamber) were in the range

  17. Synthesis and optical features of an europium organic-inorganic silicate hybrid

    Energy Technology Data Exchange (ETDEWEB)

    Franville, A.C.; Zambon, D.; Mahiou, R.; Chou, S.; Cousseins, J.C. [Universite Blaise Pascal, Aubiere (France). Lab. des Materiaux Inorganiques; Troin, Y. [Laboratoire de Chimie des Heterocycles et des Glucides, EA 987, Universite Blaise-Pascal and ENSCCF, F-63177 Aubiere Cedex (France)

    1998-07-24

    A europium organic-inorganic silicate hybrid was synthesized by grafting a coordinative group (dipicolinic acid) to a silicate network precursor (3-aminopropyltriethoxysilane) via a covalent bonding. Sol-gel process and complexation were performed using different experimental conditions. The hybrid materials, in particular the Eu{sup 3+} coordination mode, were characterized by infrared and luminescence spectroscopies. Morphology of the materials and TG analysis showed that grafted silica enhanced thermal and mechanical resistances of the organic part. (orig.) 7 refs.

  18. Net transformation of phosphorus forms applied as inorganic and organic amendments to a calcareous soil

    Science.gov (United States)

    Audette, Yuki; O'Halloran, Ivan; Voroney, Paul

    2016-04-01

    The forms of phosphorus (P) in animal manure composts are different from that of synthetic P fertilizers, and this could affect how soil P chemistry will be altered when they are used as P amendments. The objective of this study was to analyze the net changes in the nature and dynamics of plant available P forms applied either as inorganic P (KH2PO4) or turkey litter compost (TLC) in calcareous soil with and without plant growth. Forms of TLC-P were characterized by x-ray diffraction and solution 31P NMR spectroscopy techniques. The amounts of various P forms in soils were measured by a sequential fractionation method after 4, 8, 12 and 16 weeks incubation. Brushite (Ca-P) and newberyite (Mg-P) were the major forms of inorganic P, and phosphate monoester was the major form of organic P present in TLC. The addition of inorganic P fertilizer increased the labile/moderately labile P, whereas the compost increased the moderately labile P extractable with weak acid (pH 4.2). Even though the amount of the labile P fraction in the compost-treated soil was smaller than that in the fertilizer-treated soils, ryegrass growth and plant P uptake were greater. The net transformation of the labile/moderately labile P was slower in the compost-treated soil without plant growth, however it was faster with plant growth. This study showed that P applied either as an inorganic or an organic amendment was recovered in different P fractions in a calcareous soil, and therefore it is expected that the P source would affect soil P chemistry. A weak acid extractable inorganic P fraction should be considered as plant available P especially in the compost-treated soil, that is converted into plant available P through direct and/or indirect root-induced acidification in the rhizosphere.

  19. Biotransformation and detoxification of inorganic arsenic in Bombay oyster Saccostrea cucullata.

    Science.gov (United States)

    Zhang, Wei; Guo, Zhiqiang; Zhou, Yanyan; Liu, Huaxue; Zhang, Li

    2015-01-01

    Arsenic (As) exists as the toxic inorganic forms in marine water and sediment, while marine oysters usually accumulate high As contents mostly as the less toxic organic forms. It has not yet been clear that how As is biotransformed in marine oysters. This study therefore investigated the biotransformation and detoxification of two inorganic As forms (As(III) and As(V)) in Bombay oyster Saccostrea cucullata after waterborne exposures for 30 days. Seven treatments of dissolved As exposure (clean seawater, 1, 5, 20 mg/L As(III), and 1, 5, 20 mg/L As(V)) were performed. Body As concentration increased significantly after all As exposure treatments except 1mg/L As(V). Total As, As(III), and As(V) concentration were positive correlated with glutathione-S-transferases (GST) activities, suggesting GST might play an important role in the As biotransformation and detoxification process. Organic As species were predominant in control and the low As exposed oysters, whereas a large fraction of As was remained as the inorganic forms in the high As exposed oysters, suggesting As could be biotransformed efficiently in the oysters in clean or light contaminated environment. The results of As speciation demonstrated the As biotransformation in the oysters included As(V) reduction, methylation to monomethylarsonic acid (MMA) and dimethylarsinic acid (DMA), and subsequent conversion to arsenobetaine (AsB). More As was distributed in the subcellular metallothionein-like proteins fraction (MTLP) functioning sequestration and detoxification in the inorganic As exposed oysters, suggesting it was also a strategy for oysters against As stress. In summary, this study elucidated that marine oysters had high ability to accumulate, biotransform, and detoxify inorganic As.

  20. Microwave chemistry for inorganic nanomaterials synthesis.

    Science.gov (United States)

    Bilecka, Idalia; Niederberger, Markus

    2010-08-01

    This Feature Article gives an overview of microwave-assisted liquid phase routes to inorganic nanomaterials. Whereas microwave chemistry is a well-established technique in organic synthesis, its use in inorganic nanomaterials' synthesis is still at the beginning and far away from having reached its full potential. However, the rapidly growing number of publications in this field suggests that microwave chemistry will play an outstanding role in the broad field of Nanoscience and Nanotechnology. This article is not meant to give an exhaustive overview of all nanomaterials synthesized by the microwave technique, but to discuss the new opportunities that arise as a result of the unique features of microwave chemistry. Principles, advantages and limitations of microwave chemistry are introduced, its application in the synthesis of different classes of functional nanomaterials is discussed, and finally expected benefits for nanomaterials' synthesis are elaborated.

  1. Applications of inorganic nanoparticles in diabetes

    Science.gov (United States)

    Elhabush, Nada Atiya Omar

    Diabetes Mellitus (DM) is an endocrine and metabolic disease that has become a global emergency because of the rapid rise in morbidity and mortality rates worldwide. Since the direct delivery of biomolecules, such as insulin, to treat DM is inefficient and subjected to enzymatic degradation, nanotechnology and nanomedicine research have been devoted to the development of more effective methods to treat DM. Nanoparticles (NP), organic, inorganic, or hybrid, have served as potential carrier for safe and efficient transport for insulin. Additionally, several NP have biological activities that help treat and/or prevent DM and diabetes complications, such as antioxidant, anti-apoptotic, or insulin-mimetic activities. Moreover, physicochemical properties of some NP allow them to be used in diagnostic tools for potential diagnosis or monitoring purposes. This work highlights the applications of inorganic NP such as, gold, selenium, silver, calcium phosphate, zinc oxide, cerium oxide, and iron oxide and in the treatment or diagnosis of DM.

  2. QM/MM methods in inorganic chemistry.

    Science.gov (United States)

    Bo, Carles; Maseras, Feliu

    2008-06-14

    Quantum mechanics/molecular mechanics (QM/MM) methods are a useful tool for the computational study of inorganic systems. They allow a quantitative description of systems larger than those treatable with pure QM methods, in principle with a comparable quality. QM/MM calculations are being currently applied to the research in a variety of topics, including structural effects of ligand bulk, selectivity in homogeneous catalysis and mechanical embedding in heterogeneous catalysis. The QM/MM approach is also useful for the separation of steric and electronic contributions, and as an auxiliary tool for geometry optimization when full QM methods are mandatory. The power of QM/MM methods in inorganic chemistry is illustrated in this Perspective with a summary of recent representative applications.

  3. Photochromic organic-inorganic hybrid materials.

    Science.gov (United States)

    Pardo, Rosario; Zayat, Marcos; Levy, David

    2011-02-01

    Photochromic organic-inorganic hybrid materials have attracted considerable attention owing to their potential application in photoactive devices, such as optical memories, windows, photochromic decorations, optical switches, filters or non-linear optics materials. The growing interest in this field has largely expanded the use of photochromic materials for the purpose of improving existing materials and exploring new photochromic hybrid systems. This tutorial review summarizes the design and preparation of photochromic hybrid materials, and particularly those based on the incorporation of organic molecules in organic-inorganic matrices by the sol-gel method. This is the most commonly used method for the preparation of these materials as it allows vitreous hybrid materials to be obtained at low temperatures, and controls the interaction between the organic molecule and its embedding matrix, and hence allows tailoring of the performance of the resulting devices.

  4. Electrostatically gated membrane permeability in inorganic protocells

    Science.gov (United States)

    Li, Mei; Harbron, Rachel L.; Weaver, Jonathan V. M.; Binks, Bernard P.; Mann, Stephen

    2013-06-01

    Although several strategies are now available to produce functional microcompartments analogous to primitive cell-like structures, little progress has been made in generating protocell constructs with self-controlled membrane permeability. Here we describe the preparation of water-dispersible colloidosomes based on silica nanoparticles and delineated by a continuous semipermeable inorganic membrane capable of self-activated, electrostatically gated permeability. We use crosslinking and covalent grafting of a pH-responsive copolymer to generate an ultrathin elastic membrane that exhibits selective release and uptake of small molecules. This behaviour, which depends on the charge of the copolymer coronal layer, serves to trigger enzymatic dephosphorylation reactions specifically within the protocell aqueous interior. This system represents a step towards the design and construction of alternative types of artificial chemical cells and protocell models based on spontaneous processes of inorganic self-organization.

  5. Hygroscopic properties of organic and inorganic aerosols[Dissertation 17260

    Energy Technology Data Exchange (ETDEWEB)

    Sjoegren, N.O.Staffan

    2007-07-01

    The atmosphere contains gases and particulate matter (aerosol). Organic material is present both in the gas phase and in the aerosol phase. Biogenic sources such as vegetation and anthropogenic sources such as biomass burning, fossil fuel use and various industries contribute to their emissions. The study of organic compounds in aerosol particles is of importance because they affect the water uptake (hygroscopicity) of inorganic aerosol, and hence the radiation budget of the Earth through the direct and indirect aerosol effects. The hygroscopicity of mixed organic/inorganic aerosol particles produced in the laboratory was characterized. This work reports on the following substances, and mixtures of them with ammonium sulfate (AS): adipic acid (AA), citric acid (CA), glutaric acid (GA) and humic acid sodium salt (NaHA). The AA and NaHA mixtures with AS were found to require up to tens of seconds for equilibrium water content to be reached. Therefore, measurements carried out on timescales shorter than a few seconds underestimate the hygroscopic growth factor (GF) with up to 10%, for samples containing a solid phase. Conversely, the GA and CA mixtures with AS were found to take up water readily and were well described by the Zdanovskii-Stokes-Robinson (ZSR) mixing rule. The distinct deliquescence and efflorescence points of AS could be seen to gradually disappear as the CA content was increased. Furthermore mineral dust (standard Arizona test dust) was investigated, as well as the influence of nitric acid (HNO{sub 3}) uptake thereon. Mineral dust is hydrophobic, but after processing with HNO{sub 3} turns slightly hygroscopic. Large amounts of dust are injected to the atmosphere (largely from the Sahara and the Gobi deserts, but also from human land-use). Mineral dust is important as ice nuclei, and due to its larger sizes it can also contribute as cloud condensation nuclei. Mineral dust also offers surface for heterogeneous chemistry, and can play an important role

  6. Sealed Primary Lithium-Inorganic Electrolyte Cell

    Science.gov (United States)

    1977-02-01

    Battery , Thionyl Chloride , Lithium , Lithium Aluminum Chloride , Hermetic Lithium Battery , D Cell, Voltage-Delay, Shelf Life, High Energy Density Battery ... lithium - thionyl chloride , inorganic electrclyte system is one of the highest energy density systems known to date (1-4). The cells contain an Li anoae, a...However, this is not tne case with te thionyl chloride system. A completely discharged battery , while sitting on

  7. Attachment of inorganic moieties onto aliphatic polyurethanes

    OpenAIRE

    Eliane Ayres; Wander Luiz Vasconcelos; Rodrigo Lambert Oréfice

    2007-01-01

    Polyurethanes have been used in a series of applications due basically to their versatility in terms of controlling the behavior by altering basically the type of reagents used. However, for more specific and advanced applications, such as in membranes, biomaterials and sensors, well-organized and defined chemical functionalities are necessary. In this work, inorganic functionalities were incorporated into aliphatic polyurethanes (PU) having different macromolecular architectures. Polyurethan...

  8. Responses to betaine and inorganic sulphur of sheep in growth performance and fibre growth.

    Science.gov (United States)

    Nezamidoust, M; Alikhani, M; Ghorbani, G R; Edriss, M A

    2014-12-01

    Sulphur-containing amino acids (SAA) are essential and usually the first limiting amino acids for growth, milk and wool production. The keratin fibre that grows from epidermal tissue is rich in SAA. The rate of fibre growth and its S content are influenced by the availability of SAA. Betaine is a dietary source for a labile methyl group and actively participates in methionine metabolism by donating methyl groups for the remethylation of homocysteine to methionine. Ruminants are capable of synthesizing SAA from inorganic S sources, and most bacteria in the rumen can use inorganic S to meet their requirements for growth. The objective of this study was to examine whether betaine and an inorganic sulphur supplement could provide methyl groups and sulphur amino acids in a way that growth performance and wool production of ewes and lambs are improved. Treatments performed included betaine supplementation, sulphate supplementation and betaine plus sulphate supplementation with five replications for each treatment. The dry matter intake of the ewes was affected by betaine plus sulphate supplementation (p betaine plus sulphate supplementation increased (p 0.05) between treatments. In the ewes, plasma methionine concentration increased (p betaine plus sulphate treatment. No corresponding difference (p > 0.05) was observed in plasma methionine concentration in the lambs. It can be concluded that betaine plus sulphate supplementation has the potential to change wool characteristics in the ewes, while these compounds were without any effect on growth and wool production of the lambs. Combining the two supplements was advantageous.

  9. Stable colloids in molten inorganic salts

    Science.gov (United States)

    Zhang, Hao; Dasbiswas, Kinjal; Ludwig, Nicholas B.; Han, Gang; Lee, Byeongdu; Vaikuntanathan, Suri; Talapin, Dmitri V.

    2017-02-01

    A colloidal solution is a homogeneous dispersion of particles or droplets of one phase (solute) in a second, typically liquid, phase (solvent). Colloids are ubiquitous in biological, chemical and technological processes, homogenizing highly dissimilar constituents. To stabilize a colloidal system against coalescence and aggregation, the surface of each solute particle is engineered to impose repulsive forces strong enough to overpower van der Waals attraction and keep the particles separated from each other. Electrostatic stabilization of charged solutes works well in solvents with high dielectric constants, such as water (dielectric constant of 80). In contrast, colloidal stabilization in solvents with low polarity, such as hexane (dielectric constant of about 2), can be achieved by decorating the surface of each particle of the solute with molecules (surfactants) containing flexible, brush-like chains. Here we report a class of colloidal systems in which solute particles (including metals, semiconductors and magnetic materials) form stable colloids in various molten inorganic salts. The stability of such colloids cannot be explained by traditional electrostatic and steric mechanisms. Screening of many solute–solvent combinations shows that colloidal stability can be traced to the strength of chemical bonding at the solute–solvent interface. Theoretical analysis and molecular dynamics modelling suggest that a layer of surface-bound solvent ions produces long-ranged charge-density oscillations in the molten salt around solute particles, preventing their aggregation. Colloids composed of inorganic particles in inorganic melts offer opportunities for introducing colloidal techniques to solid-state science and engineering applications.

  10. Flexible Hybrid Organic-Inorganic Perovskite Memory.

    Science.gov (United States)

    Gu, Chungwan; Lee, Jang-Sik

    2016-05-24

    Active research has been done on hybrid organic-inorganic perovskite materials for application to solar cells with high power conversion efficiency. However, this material often shows hysteresis, which is undesirable, shift in the current-voltage curve. The hysteresis may come from formation of defects and their movement in perovskite materials. Here, we utilize the defects in perovskite materials to be used in memory operations. We demonstrate flexible nonvolatile memory devices based on hybrid organic-inorganic perovskite as the resistive switching layer on a plastic substrate. A uniform perovskite layer is formed on a transparent electrode-coated plastic substrate by solvent engineering. Flexible nonvolatile memory based on the perovskite layer shows reproducible and reliable memory characteristics in terms of program/erase operations, data retention, and endurance properties. The memory devices also show good mechanical flexibility. It is suggested that resistive switching is done by migration of vacancy defects and formation of conducting filaments under the electric field in the perovskite layer. It is believed that organic-inorganic perovskite materials have great potential to be used in high-performance, flexible memory devices.

  11. Inorganic particle analysis of dental impression elastomers.

    Science.gov (United States)

    Carlo, Hugo Lemes; Fonseca, Rodrigo Borges; Soares, Carlos José; Correr, Américo Bortolazzo; Correr-Sobrinho, Lourenço; Sinhoreti, Mário Alexandre Coelho

    2010-01-01

    The aim of this study was to determine quantitatively and qualitatively the inorganic particle fraction of commercially available dental elastomers. The inorganic volumetric fraction of two addition silicones (Reprosil Putty/Fluid and Flexitime Easy Putty/Fluid), three condensation silicones (Clonage Putty/Fluid, Optosil Confort/Xantopren VL and Silon APS Putty/Fluid), one polyether (Impregum Soft Light Body) and one polysulfide (Permlastic Light Body) was accessed by weighing a previously determined mass of each material in water before and after burning samples at 600 ºC, during 3 h. Unsettled material samples were soaked in acetone and chloroform for removal of the organic portion. The remaining filler particles were sputter-coated with gold evaluation of their morphology and size, under scanning electron microscopy (SEM). Flexitime Easy Putty was the material with the highest results for volumetric particle fraction, while Impregum Soft had the lowest values. Silon 2 APS Fluid presented the lowest mean filler size values, while Clonage Putty had the highest values. SEM micrographs of the inorganic particles showed several morphologies - lathe-cut, spherical, spherical-like, sticks, and sticks mixed to lathe-cut powder. The results of this study revealed differences in particle characteristics among the elastometic materials that could lead to different results when testing mechanical properties.

  12. Fabricating porous materials using interpenetrating inorganic-organic composite gels

    Science.gov (United States)

    Seo, Dong-Kyun; Volosin, Alex

    2016-06-14

    Porous materials are fabricated using interpenetrating inorganic-organic composite gels. A mixture or precursor solution including an inorganic gel precursor, an organic polymer gel precursor, and a solvent is treated to form an inorganic wet gel including the organic polymer gel precursor and the solvent. The inorganic wet gel is then treated to form a composite wet gel including an organic polymer network in the body of the inorganic wet gel, producing an interpenetrating inorganic-organic composite gel. The composite wet gel is dried to form a composite material including the organic polymer network and an inorganic network component. The composite material can be treated further to form a porous composite material, a porous polymer or polymer composite, a porous metal oxide, and other porous materials.

  13. Conjunctive and mineralization impact of municipal solid waste compost and inorganic fertilizer on lysimeter and pot studies.

    Science.gov (United States)

    Khalid, Iqbal; Nadeem, Amana; Ahmed, Rauf; Husnain, Anwer

    2014-01-01

    Objectives of the present study were to investigate the physico-chemical properties of municipal solid waste (MSW)-enriched compost and its effect on nutrient mineralization and subsequent plant growth. The enrichment of MSW compost by inorganic salts enhanced the humification rate and reduced the carbon nitrogen (C/N) ratio in less time than control compost. The chemical properties of compost, C/N ratio, humic acid, fulvic acid, degree of polymerization and humification index revealed the significant correlation amid properties. A laboratory-scale experiment evaluated the conjunctive effect of MSW compost and inorganic fertilizer on tomato plants in a pot experiment. In the pot experiment five treatments, Inorganic fertilizer (T1), enriched compost (T2), enriched compost 80% + 20% inorganic fertilizer (T3), enriched compost 60% + 40% inorganic fertilizer (T4) were defined including control (Ts), applied at the rate of 110 kg-N/ha and results revealed that all treatments significantly enhanced horticultural production of tomato plant; however T4 was most effectual as compared with control, T1, T2 and T3. Augmentation in organic matter and available phosphorus (P) potassium (K) and nitrogen (N) were also observed in compost treatments. The leachability and phytoavailability of phosphorus (P), potassium (K) and nitrogen (N) from sandy soil, amended with enriched, control compost and inorganic fertilizer at rates of 200, 400 and 600 kg-N/ha were evaluated in a lysimeter study. Results illustrated that concentration of mineral nitrogen was elevated in the leachate of inorganic fertilizer than enriched and control composts; therefore compost fortifies soil with utmost nutrients for plants' growth.

  14. Fouling of inorganic membrane and flux enhancement in membrane-coupled anaerobic bioreactor

    Energy Technology Data Exchange (ETDEWEB)

    Yoon, S.H.; Kang, I.J.; Lee, C.H. [Seoul National Univ. (Korea, Republic of). Dept. of Chemical Technology

    1999-03-01

    The fouling mechanism of an inorganic membrane was studied during the operation of a membrane-coupled anaerobic bioreactor (MCAB) when alcohol distillery wastewater was used as a digester feed. It was observed that the fouling mechanism of an inorganic membrane was significantly different from that of conventional membrane filtration processes. The main foulant was identified to be an inorganic precipitate, struvite (MgNH{sub 4}PO{sub 4}{center_dot}6H{sub 2}O), rather than anaerobic microbial flocs. Struvite appears to be precipitated not only on the membrane surface but also inside the membrane pores. The amount of struvite generated during the bioreaction was estimated to be about 2 g/L alcohol distillery wastewater. The inorganic foulant was not easily removed by general physical cleaning such as depressurization, lumen flushing, and backflushing. Based on these findings, the membrane fouling was alleviated and thus flux was enhanced by adopting a backfeeding mode which has dual purpose of feeding and backflushing with particle-free acidic wastewater used as the feed for anaerobic digestion.

  15. Accuracy of a method based on atomic absorption spectrometry to determine inorganic arsenic in food: Outcome of the collaborative trial IMEP-41

    DEFF Research Database (Denmark)

    Fiamegkos, I.; Cordeiro, F.; Robouch, P.;

    2016-01-01

    the release of all arsenic species into solution, and (ii) subsequent extraction of the inorganic arsenic present in the acid medium using chloroform followed by back-extraction to acidic medium. The final detection and quantification is done by flow injection hydride generation atomic absorption spectrometry......A collaborative trial was conducted to determine the performance characteristics of an analytical method for the quantification of inorganic arsenic (iAs) in food. The method is based on (i) solubilisation of the protein matrix with concentrated hydrochloric acid to denature proteins and allow...

  16. Inorganic-based proton conductive composite membranes for elevated temperature and reduced relative humidity PEM fuel cells

    Science.gov (United States)

    Wang, Chunmei

    Proton exchange membrane (PEM) fuel cells are regarded as highly promising energy conversion systems for future transportation and stationary power generation and have been under intensive investigations for the last decade. Unfortunately, cutting edge PEM fuel cell design and components still do not allow economically commercial implementation of this technology. The main obstacles are high cost of proton conductive membranes, low-proton conductivity at low relative humidity (RH), and dehydration and degradation of polymer membranes at high temperatures. The objective of this study was to develop a systematic approach to design a high proton conductive composite membrane that can provide a conductivity of approximately 100 mS cm-1 under hot and dry conditions (120°C and 50% RH). The approach was based on fundamental and experimental studies of the proton conductivity of inorganic additives and composite membranes. We synthesized and investigated a variety of organic-inorganic Nafion-based composite membranes. In particular, we analyzed their fundamental properties, which included thermal stability, morphology, the interaction between inorganic network and Nafion clusters, and the effect of inorganic phase on the membrane conductivity. A wide range of inorganic materials was studied in advance in order to select the proton conductive inorganic additives for composite membranes. We developed a conductivity measurement method, with which the proton conductivity characteristics of solid acid materials, zirconium phosphates, sulfated zirconia (S-ZrO2), phosphosilicate gels, and Santa Barbara Amorphous silica (SBA-15) were discussed in detail. Composite membranes containing Nafion and different amounts of functionalized inorganic additives (sulfated inorganics such as S-ZrO2, SBA-15, Mobil Composition of Matter MCM-41, and S-SiO2, and phosphonated inorganic P-SiO2) were synthesized with different methods. We incorporated inorganic particles within Nafion clusters

  17. NUTRITIONAL AND BAKING QUALITY OF LOW PHYTIC ACID WHEAT

    Science.gov (United States)

    Phytic acid is the major storage form of phosphorus in wheat grain. Non-ruminant animals cannot utilize phytic acid phosphorus, and phytic acid reduces the nutritional availability of important minerals. We have identified a wheat mutant (Lpa1-1) with reduced phytic acid P and increased inorganic ...

  18. Fractionation of inorganic arsenic by adjusting hydrogen ion concentration.

    Science.gov (United States)

    Oliveira, Andrea; Gonzalez, Mario Henrique; Queiroz, Helena Müller; Cadore, Solange

    2016-12-15

    The inorganic fraction of arsenic species, iAs=∑[As(III)+As(V)] present in fish samples can be quantified in the presence of other arsenic species also found in fishes, such as: monomethylarsonic acid (MMA), dimethylarsinic acid (DMA) and arsenobetaine (AsB). The toxic arsenic fraction was selected taking into account the dissociation constants of these arsenic species in different hydrogen ions concentration leading to the arsine formation from iAs compounds detected as As(III) by HG AAS. For thus, a microwave assisted extraction was carried out using HCl 1molL(-1) in order to maintain the integrity of the arsenic species in this mild extraction media. Recovery experiments were done for iAs fraction, in the presence of other arsenic species. The recovery values obtained for iAs fraction added were quantitative about 87-107% (for N=3, RSD⩽3%). The limit of detection (LOD), and the limit of quantification (LOQ), were 5μgkg(-1) and 16μgkg(-1) respectively.

  19. Multifunctional slow-release organic-inorganic compound fertilizer.

    Science.gov (United States)

    Ni, Boli; Liu, Mingzhu; Lü, Shaoyu; Xie, Lihua; Wang, Yanfang

    2010-12-08

    Multifunctional slow-release organic-inorganic compound fertilizer (MSOF) has been investigated to improve fertilizer use efficiency and reduce environmental pollution derived from fertilizer overdosage. The special fertilizer is based on natural attapulgite (APT) clay used as a matrix, sodium alginate used as an inner coating and sodium alginate-g-poly(acrylic acid-co-acrylamide)/humic acid (SA-g-P(AA-co-AM)/HA) superabsorbent polymer used as an outer coating. The coated multielement compound fertilizer granules were produced in a pan granulator, and the diameter of the prills was in the range of 2.5-3.5 mm. The structural and chemical characteristics of the product, as well as its efficiency in slowing the nutrients release, were examined. In addition, a mathematical model for nutrient release from the fertilizer was applied to calculate the diffusion coefficient D of nutrients in MSOF. The degradation of the SA-g-P(AA-co-AM)/HA coating was assessed by examining the weight loss with incubation time in soil. It is demonstrated that the product prepared by a simple route with good slow-release property may be expected to have wide potential applications in modern agriculture and horticulture.

  20. Organic materials as templates for the formation of mesoporous inorganic materials and ordered inorganic nanocomposites

    Science.gov (United States)

    Ziegler, Christopher R.

    Hierarchically structured inorganic materials are everywhere in nature. From unicellular aquatic algae such as diatoms to the bones and/or cartilage that comprise the skeletal systems of vertebrates. Complex mechanisms involving site-specific chemistries and precision kinetics are responsible for the formation of such structures. In the synthetic realm, reproduction of even the most basic hierarchical structure effortlessly produced in nature is difficult. However, through the utilization of self-assembling structures or "templates", such as polymers or amphiphilic surfactants, combined with some favorable interaction between a chosen inorganic, the potential exists to imprint an inorganic material with a morphology dictated via synthetic molecular self-assembly. In doing so, a very basic hierarchical structure is formed on the angstrom and nanometer scales. The work presented herein utilizes the self-assembly of either surfactants or block copolymers with the desired inorganic or inorganic precursor to form templated inorganic structures. Specifically, mesoporous silica spheres and copolymer directed calcium phosphate-polymer composites were formed through the co-assembly of an organic template and a precursor to form the desired mesostructured inorganic. For the case of the mesoporous silica spheres, a silica precursor was mixed with cetyltrimethylammonium bromide and cysteamine, a highly effective biomimetic catalyst for the conversion of alkoxysilanes to silica. Through charge-based interactions between anionic silica species and the micelle-forming cationic surfactant, ordered silica structures resulted. The incorporation of a novel, effective catalyst was found to form highly condensed silica spheres for potential application as catalyst supports or an encapsulation media. Ordered calcium phosphate-polymer composites were formed using two routes. Both routes take advantage of hydrogen bonding and ionic interactions between the calcium and phosphate precursors

  1. EFFECT OF CASEIN-BASED SEMISYNTHETIC FOOD ON RENAL ACID EXCRETION AND ACID-BASE STATE OF BLOOD IN DOGS

    NARCIS (Netherlands)

    ZIJLSTRA, WG; LANGBROEK, AJM; KRAAN, J; RISPENS, P; NIJMEIJER, A

    1995-01-01

    Urinary acid excretion and blood acid-base stare were determined in dogs fed a casein-based semi-synthetic food (SSF), to which different amounts of salts had been added, in comparison with feeding normal dog food. Net acid excretion (NAE) and inorganic acid excretion (IAE) increased during SSF feed

  2. Designing an optimally proportional inorganic scintillator

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Jai, E-mail: jai.singh@cdu.edu.au [School of Engineering and IT, B-Purple-12, Faculty of EHSE, Charles Darwin University, NT 0909 (Australia); Koblov, Alexander [School of Engineering and IT, B-Purple-12, Faculty of EHSE, Charles Darwin University, NT 0909 (Australia)

    2012-09-01

    The nonproportionality observed in the light yield of inorganic scintillators is studied theoretically as a function of the rates of bimolecular and Auger quenching processes occurring within the electron track initiated by a gamma- or X-ray photon incident on a scintillator. Assuming a cylindrical track, the influence of the track radius and concentration of excitations created within the track on the scintillator light yield is also studied. Analysing the calculated light yield a guideline for inventing an optimally proportional scintillator with optimal energy resolution is presented.

  3. Magnetic field processing of inorganic polymers

    Energy Technology Data Exchange (ETDEWEB)

    Kunerth, D.C.; Peterson, E.S. [Idaho National Engineering Laboratory, Idaho Falls, ID (United States)

    1995-05-01

    The purpose of this project is to investigate, understand, and demonstrate the use of magnetic field processing (MFP) to modify the properties of inorganic-based polymers and to develop the basic technical knowledge required for industrial implementation. Polyphosphazene membranes for chemical separation applications are being emphasized by this project. Previous work demonstrated that magnetic fields, appropriately applied during processing, can be used to beneficially modify membrane morphology. MFP membranes have significantly increased flux capabilities while maintaining the same chemical selectivity as the unprocessed membranes.

  4. Stretchable, curvilinear electronics based on inorganic materials.

    Science.gov (United States)

    Kim, Dae-Hyeong; Xiao, Jianliang; Song, Jizhou; Huang, Yonggang; Rogers, John A

    2010-05-18

    All commercial forms of electronic/optoelectronic technologies use planar, rigid substrates. Device possibilities that exploit bio-inspired designs or require intimate integration with the human body demand curvilinear shapes and/or elastic responses to large strain deformations. This article reviews progress in research designed to accomplish these outcomes with established, high-performance inorganic electronic materials and modest modifications to conventional, planar processing techniques. We outline the most well developed strategies and illustrate their use in demonstrator devices that exploit unique combinations of shape, mechanical properties and electronic performance. We conclude with an outlook on the challenges and opportunities for this emerging area of materials science and engineering.

  5. Nanoscale investigation of organic - inorganic halide perovskites

    Science.gov (United States)

    Cacovich, S.; Divitini, G.; Vrućinić, M.; Sadhanala, A.; Friend, R. H.; Sirringhaus, H.; Deschler, F.; Ducati, C.

    2015-10-01

    Over the last few years organic - inorganic halide perovskite-based solar cells have exhibited a rapid evolution, reaching certified power conversion efficiencies now surpassing 20%. Nevertheless the understanding of the optical and electronic properties of such systems on the nanoscale is still an open problem. In this work we investigate two model perovskite systems (based on iodine - CH3NH3PbI3 and bromine - CH3NH3PbBr3), analysing the local elemental composition and crystallinity and identifying chemical inhomogeneities.

  6. A robotics-based automated assay for inorganic and organic phosphates.

    Science.gov (United States)

    Cogan, E B; Birrell, G B; Griffith, O H

    1999-06-15

    Phosphate analyses are fundamental to a broad range of biochemical applications involving inorganic phosphate and organic phosphoesters such as phospholipids, phosphorylated proteins, and nucleic acids. A practical automated method utilizing robotics is described in this report. Five colorimetric methods of phosphate analyses based on formation of a phosphomolybdate complex and compatible with the automated assay were tested, and the fundamental chemistry is discussed. The relative sensitivities are malachite green > crystal violet > quinaldine red > ascorbate reduction > antimony-modified ascorbate reduction, although only a fourfold improvement was observed in going from the modified ascorbate procedure to malachite green. Malachite green was selected to optimize the assay because this dye provided the highest sensitivity. However, where color stability and low blanks are more important than sensitivity, the ascorbate reduction and quinaldine red methods were found to be better choices than malachite green. Automation using a robotic liquid-handling system substantially reduces the labor required to process large arrays of samples. The result is a sensitive, nonradioactive assay of inorganic phosphate with high throughput. A digestion step in an acid-resistant 96-well plate was developed to extend the assay to phosphate esters. The robotic-based assay was demonstrated with inorganic phosphate and a common phospholipid, phosphatidylcholine.

  7. A thermodynamic model of mixed organic-inorganic aerosols to predict activity coefficients

    Science.gov (United States)

    Zuend, A.; Marcolli, C.; Luo, B. P.; Peter, T.

    2008-08-01

    Tropospheric aerosols contain mixtures of inorganic salts, acids, water, and a large variety of organic compounds. Interactions between these substances in liquid mixtures lead to discrepancies from ideal thermodynamic behaviour. By means of activity coefficients, non-ideal behaviour can be taken into account. We present here a thermodynamic model named AIOMFAC (Aerosol Inorganic-Organic Mixtures Functional groups Activity Coefficients) that is able to calculate activity coefficients covering inorganic, organic, and organic-inorganic interactions in aqueous solutions over a wide concentration range. This model is based on the activity coefficient model LIFAC by Yan et al. (1999) that we modified and reparametrised to better describe atmospherically relevant conditions and mixture compositions. Focusing on atmospheric applications we considered H+, Li+, Na+, K+, NH+4, Mg2+, Ca2+, Cl-, Br-, NO-3, HSO-4, and SO2-4 as cations and anions and a wide range of alcohols/polyols composed of the functional groups CHn and OH as organic compounds. With AIOMFAC, the activities of the components within an aqueous electrolyte solution are well represented up to high ionic strength. Most notably, a semi-empirical middle-range parametrisation of direct organic-inorganic interactions in alcohol+water+salt solutions strongly improves the agreement between experimental and modelled activity coefficients. At room temperature, this novel thermodynamic model offers the possibility to compute equilibrium relative humidities, gas/particle partitioning and liquid-liquid phase separations with high accuracy. In further studies, other organic functional groups will be introduced. The model framework is not restricted to specific ions or organic compounds and is therefore also applicable for other research topics.

  8. A thermodynamic model of mixed organic-inorganic aerosols to predict activity coefficients

    Directory of Open Access Journals (Sweden)

    A. Zuend

    2008-08-01

    Full Text Available Tropospheric aerosols contain mixtures of inorganic salts, acids, water, and a large variety of organic compounds. Interactions between these substances in liquid mixtures lead to discrepancies from ideal thermodynamic behaviour. By means of activity coefficients, non-ideal behaviour can be taken into account. We present here a thermodynamic model named AIOMFAC (Aerosol Inorganic-Organic Mixtures Functional groups Activity Coefficients that is able to calculate activity coefficients covering inorganic, organic, and organic-inorganic interactions in aqueous solutions over a wide concentration range. This model is based on the activity coefficient model LIFAC by Yan et al. (1999 that we modified and reparametrised to better describe atmospherically relevant conditions and mixture compositions. Focusing on atmospheric applications we considered H+, Li+, Na+, K+, NH+4, Mg2+, Ca2+, Cl, Br, NO3, HSO4, and SO2−4 as cations and anions and a wide range of alcohols/polyols composed of the functional groups CHn and OH as organic compounds. With AIOMFAC, the activities of the components within an aqueous electrolyte solution are well represented up to high ionic strength. Most notably, a semi-empirical middle-range parametrisation of direct organic-inorganic interactions in alcohol+water+salt solutions strongly improves the agreement between experimental and modelled activity coefficients. At room temperature, this novel thermodynamic model offers the possibility to compute equilibrium relative humidities, gas/particle partitioning and liquid-liquid phase separations with high accuracy. In further studies, other organic functional groups will be introduced. The model framework is not restricted to specific ions or organic compounds and is therefore also

  9. [Effect of inorganic carbon source on lipid production with autotrophic Chlorella vulgaris].

    Science.gov (United States)

    Zheng, Hongli; Gao, Zhen; Zhang, Qi; Huang, He; Ji, Xiaojun; Sun, Honglei; Dou, Chang

    2011-03-01

    We studied the effects of three inorganic carbon sources, Na2CO3, NaHCO3 and CO2, and their initial concentrations on lipid production of Chlorella vulgaris. Chlorella vulgaris could utilize Na2CO3, NaHCO3 and CO2 to produce lipids. After 10-day cultivation with each of the three inorganic carbon sources, lipid yield of Chlorella vulgaris reached its peak with the concentration increase of the inorganic carbon source, but dropped again by further increase of the concentration. The pH value of the culture medium for Chlorella vulgaris increased after the cultivation on inorganic carbon source. The optimal concentration of both Na2CO3 and NaHCO3 was 40 mmol/L, and their corresponding biomass dry weight was 0.52 g/L and 0.67 g/L with their corresponding lipid yield 0.19 g/L and 0.22 g/L. When the concentration of CO2 was 6%, Chlorella vulgaris grew the fastest and its biomass dry weight was 2.42 g/L with the highest lipid yield of 0.72 g/L. When the concentration of CO2 was too low, the supply of inorganic carbon was insufficient and lipid yield was low. A too high concentration of CO2 caused a low pH and lipid accumulation was inhibited. Na2CO3 and NaHCO3 were more favorable for Chlorella vulgaris to accumulate unsaturated fatty acids than that of CO2.

  10. Part 6: The Literature of Inorganic Chemistry, Revised.

    Science.gov (United States)

    Douville, Judith A.

    2002-01-01

    Presents a list of resources on inorganic chemistry that includes general surveys, nomenclature, dictionaries, handbooks, compilations, and treatises. Selected for use by academic and student chemists. (DDR)

  11. One-Dimensional Organic-Inorganic Nanocomposite Synthesized with Single-Walled Carbon Nanotube Templates

    Directory of Open Access Journals (Sweden)

    Wei Li

    2014-08-01

    Full Text Available This study reports on single-walled carbon nanotubes (SWCNT as templates for the preparation of 1D porous organic-inorganic hybrid composites. The in situ deposited SWCNT were sputter coated with Sn metal and thermally oxidized in air to form a SnO2/SWCNT nanowire framework on SiO2/Si substrate. Poly(acrylic acid (PAA was coated onto this scaffold through UV light-induced radical polymerization, which resulted in the final formation of hybrid composites. The structures of hybrid composites were investigated by scanning electron microscopy, transmission electron microscopy, infrared spectroscopy, and Raman spectroscopy. The results show that PAA was successfully coated and the structural advantage of nanowire was fairly maintained, which indicates that this framework is very stable for organic functionalization in solution. The simplicity of this method for the formation of porous organic-inorganic hybrid composites provides a potential application for nanoelectronic devices.

  12. Inorganic arsenic - SPE HG-AAS method for RICE tested in-house and collaboratively

    DEFF Research Database (Denmark)

    Rasmussen, Rie Romme; Qian, Yiting; Sloth, Jens Jørgen

    and DMA) was done by off-line solidphase extraction (SPE) followed by hydride generation atomic absorption spectrometry (HG-AAS) detection. Water bath heating (90 °C, 60 min) of samples with dilute nitric acid and hydrogen peroxide solubilised and oxidized all iAs to arsenate (AsV). Loading of buffered......Arsenic (As) is a trace element present in the environment and consequently in various food items, e.g. rice, which may contain relatively high concentration of arsenic compared to other foodstuffs of plant origin. Rice contains most often three forms of arsenic; inorganic arsenic (i...... and is one of the major contributors to the iAs exposure in many countries. The work presented here describes the development, validation and application of a simple and inexpensive method for inorganic arsenic (iAs) determination in rice samples. The separation of iAs from organoarsenic compounds (MA...

  13. Changes in the inorganic status and enzyme activities in senescent leaves of chickpea, Cicer arietinum L.

    Directory of Open Access Journals (Sweden)

    Chandrashekkhar V. Murumkar

    2014-01-01

    Full Text Available The changes in the level of some inorganic constituents and the activities of some important enzyme systems in senescent leaves of chickpea (Cicer arietinum L. have been studied. In senescent leaves, a marked decline in the potassium and phosphorus contents was evident which was accompanied by the accumulation of calcium, silicon, chloride and manganese. Leaf senescence was accompanied by a great increase in hydrolytic processes, as revealed by the increase in the activities of acid phosphatase, alkaline phosphatase, ATPase, inorganic pyrophosphatase and 3-phosphoglycerate phosphatase. The activities of nitrogen metabolism enzymes, namely nitrate reductase, nitrite reductase, glutamine synthetase and alanine aminotransferase, and of photorespiratory enzymes -- phosphoglycolate phosphatase, glycolate oxidase and catalase, were lower in senescent leaves. Leaf senescence was further associated with an increase in the activities of peroxidase and polyphenol oxidase, a considerable depression in pyruvate kinase activity, and a slight elevation in aldolase activity.

  14. Inorganic Surface Modification of Nonwoven Polymeric Substrates

    Science.gov (United States)

    Halbur, Jonathan Chandler

    In this study, atomic layer deposition (ALD), a vapor phase inorganic thin film deposition technique, is used to modify the surface of a range of industrially relevant polymers to enhance surface properties or impart additional functionalities. Several unique demonstrations of polymer surface modification are presented including uniform nanomaterial photodeposition to the surface of nonowoven fabrics and the first application of photocatalytic thin film coated nonwovens for advanced filtration of heavy metals from solution. Recent advances in polymer synthesis and processing technologies have resulted in the production of novel polymer systems with unique chemistries and sub-micron scale dimensions. As a result, advanced fiber systems have received much attention for potential use in a wide range of industrially and medically important applications such as advanced and selective filtration, catalysis, flexible electronics, and tissue engineering. However, tailoring the surface properties of the polymer is still needed in order to realize the full range of advanced applications, which can be difficult given the high complexity and non-uniformity of nonwoven polymeric structures. Uniform and controllable inorganic surface modification of nonwovens allows the introduction or modification of many crucial polymer properties with a wide range of application methods.

  15. Applications of Raman Spectroscopy to Inorganic Chemistry

    Institute of Scientific and Technical Information of China (English)

    RobinJHClarkFRS

    1995-01-01

    The renaissance in Raman spectroscopy some 25-30 years ago had particular and immediate impact on Inorganic Chemistry,viz in areas such as the study of deeply coloued compounds,structural changes on change of state,equilibria,vapour phase band contour analysis,Raman band intensities and the nature of the chemical bond,metal-metal bonding,species in melts,identification of species in solution and of radicals by time-resolved techniques,in bioinorganic chemistry,and of linear-chain semiconductors.More recently,much attention has been directed at the quantitative level at the evaluation of geometric changes in molecules on excitation by resonance Raman spectroscopy.At the qualitative level Raman microscopy is now recognised to be the most effective technique for the identification of pigments-particularly the inorganic ones-on medieval manuscripts and especially of the components(down to grain sizes of -1 um)of pigment mixtures,It is thus a very important technique at the Arts/Science borderling in conservation science.

  16. Polyoxometalates: from inorganic chemistry to materials science.

    Science.gov (United States)

    Casañ-Pastor, Nieves; Gómez-Romero, Pedro

    2004-05-01

    Polyoxometalates have been traditionally the subject of study of molecular inorganic chemistry. Yet, these polynuclear molecules, reminiscent of oxide clusters, present a wide range of structures and with them ideal frameworks for the deployment of a plethora of useful magnetic, electroionic, catalytic, bioactive and photochemical properties. With this in mind, a new trend towards the application of these remarkable species in materials science is beginning to develop. In this review we analyze this trend and discuss two main lines of thought for the application of polyoxometalates as materials. On the one hand, there is their use as clusters with inherently useful properties on themselves, a line which has produced fundamental studies of their magnetic, electronic or photoelectrochemical properties and has shown these clusters as models for quantum-sized oxides. On the other hand, the encapsulation or integration of polyoxometalates into organic, polymeric or inorganic matrices or substrates opens a whole new field within the area of hybrid materials for harnessing the multifunctional properties of these versatile species in a wide variety of applications, ranging from catalysis to energy storage to biomedicine.

  17. From stretchable to reconfigurable inorganic electronics

    KAUST Repository

    Nassar, Joanna M.

    2016-05-06

    Today’s state-of-the-art electronics are high performing, energy efficient, multi-functional and cost effective. However, they are also typically rigid and brittle. With the emergence of the Internet of Everything, electronic applications are expanding into previously unexplored areas, like healthcare, smart wearable artifacts, and robotics. One major challenge is the physical asymmetry of target application surfaces, which often cause mechanical stretching, contracting, twisting and other deformations to the application. In this review paper, we explore materials, processes, mechanics and devices that enable physically stretchable and reconfigurable electronics. While the concept of stretchable electronics is commonly used in practice, the notion of physically reconfigurable electronics is still in its infancy. Because organic materials are commonly naturally stretchable and physically deformable, we predominantly focus on electronics made from inorganic materials that have the capacity for physical stretching and reconfiguration while retaining their intended attributes. We emphasize how applications of electronics dictate theory to integration strategy for stretchable and reconfigurable inorganic electronics.

  18. Organic-inorganic random copolymers from methacrylate-terminated poly(ethylene oxide) with 3-methacryloxypropylheptaphenyl polyhedral oligomeric silsesquioxane: synthesis via RAFT polymerization and self-assembly behavior.

    Science.gov (United States)

    Wei, Kun; Li, Lei; Zheng, Sixun; Wang, Ge; Liang, Qi

    2014-01-14

    In this contribution, we report the synthesis of organic-inorganic random polymers from methacrylate-terminated poly(ethylene oxide) (MAPEO) (Mn = 950) and 3-methacryloxypropylheptaphenyl polyhedral oligomeric silsesquioxane (MAPOSS) macromers via reversible addition-fragmentation chain transfer (RAFT) polymerization with 4-cyano-4-(thiobenzoylthio) valeric acid (CTBTVA) as the chain transfer agent. The organic-inorganic random copolymers were characterized by means of (1)H NMR spectroscopy, gel permeation chromatography (GPC) and differential scanning calorimetry (DSC). The results of GPC indicate that the polymerizations were carried out in a controlled fashion. Transmission electron microscopy (TEM) showed that the organic-inorganic random copolymers in bulk were microphase-separated and the POSS microdomains were formed via POSS-POSS interactions. In aqueous solutions the organic-inorganic random copolymers were capable of self-assembling into spherical nanoobjects as evidenced by transmission electron microscopy (TEM) and dynamic laser scattering (DLS). The self-assembly behavior of the organic-inorganic random copolymers was also found to occur in the mixtures with the precursors of epoxy. The nanostructures were further fixed via subsequent curing reaction and thus the organic-inorganic nanocomposites were obtained. The formation of nanophases in epoxy thermosets was confirmed by transmission electron microscopy (TEM) and dynamic mechanical thermal analysis (DMTA). The organic-inorganic nanocomposites displayed the enhanced surface hydrophobicity as evidenced by surface contact angle measurements.

  19. Methyl mercury, but not inorganic mercury, associated with higher blood pressure during pregnancy.

    Science.gov (United States)

    Wells, Ellen M; Herbstman, Julie B; Lin, Yu Hong; Hibbeln, Joseph R; Halden, Rolf U; Witter, Frank R; Goldman, Lynn R

    2017-04-01

    Prior studies addressing associations between mercury and blood pressure have produced inconsistent findings; some of this may result from measuring total instead of speciated mercury. This cross-sectional study of 263 pregnant women assessed total mercury, speciated mercury, selenium, and n-3 polyunsaturated fatty acids in umbilical cord blood and blood pressure during labor and delivery. Models with a) total mercury or b) methyl and inorganic mercury were evaluated. Regression models adjusted for maternal age, race/ethnicity, prepregnancy body mass index, neighborhood income, parity, smoking, n-3 fatty acids and selenium. Geometric mean total, methyl, and inorganic mercury concentrations were 1.40µg/L (95% confidence interval: 1.29, 1.52); 0.95µg/L (0.84, 1.07); and 0.13µg/L (0.10, 0.17), respectively. Elevated systolic BP, diastolic BP, and pulse pressure were found, respectively, in 11.4%, 6.8%, and 19.8% of mothers. In adjusted multivariable models, a one-tertile increase of methyl mercury was associated with 2.83mmHg (0.17, 5.50) higher systolic blood pressure and 2.99mmHg (0.91, 5.08) higher pulse pressure. In the same models, an increase of one tertile of inorganic mercury was associated with -1.18mmHg (-3.72, 1.35) lower systolic blood pressure and -2.51mmHg (-4.49, -0.53) lower pulse pressure. No associations were observed with diastolic pressure. There was a non-significant trend of higher total mercury with higher systolic blood pressure. We observed a significant association of higher methyl mercury with higher systolic and pulse pressure, yet higher inorganic mercury was significantly associated with lower pulse pressure. These results should be confirmed with larger, longitudinal studies.

  20. Water soluble inorganic trace gases and related aerosol compounds in the tropical boundary layer. An analysis based on real time measurements at a pasture site in the Amazon Basin

    NARCIS (Netherlands)

    Trebs, I.

    2005-01-01

    This dissertation investigates the behavior of water-soluble inorganic trace gases and related aerosol species in the tropical boundary layer. Mixing ratios of ammonia (NH3), nitric acid (HNO3), nitrous acid (HONO), hydrochloric acid (HCl), sulfur dioxide (SO;,) and the corresponding water-soluble a

  1. Survey of organic acid eluents for anion chromatography

    Energy Technology Data Exchange (ETDEWEB)

    Book, D.E.

    1981-10-01

    Of all the potential eluents surveyed (including aromatic, sulfonic, phosphonic, among other acids), only the carboxylic acids and the nitrophenols are recommended as eluents for anion chromatography. The concentration of the eluent should be in the range 5 x 10/sup -5/ to 1 x 10/sup -3/ M. The eluent should have the same charge as inorganic anions, a higher charge than organic acid samples. Choice of eluents for separation of halides, chloride and sulfate, multivalent inorganic anions, small alkyl acids, and aromatic acids is discussed. (DLC)

  2. AC electrophoretic deposition of organic-inorganic composite coatings.

    Science.gov (United States)

    Yoshioka, T; Chávez-Valdez, A; Roether, J A; Schubert, D W; Boccaccini, A R

    2013-02-15

    Alternating current electrophoretic deposition (AC-EPD) of polyacrylic acid (PAA)-titanium oxide (TiO(2)) nanoparticle composites on stainless steel electrodes was investigated in basic aqueous solution. AC square wave with duty cycle of 80% was applied at a frequency of 1 kHz. FTIR-ATR spectra showed that both AC and direct current (DC) EPD successfully deposited PAA-TiO(2) composites. The deposition rate using AC-EPD was lower than that obtained in direct current DC-EPD. However, the microstructure and surface morphology of the deposited composite coatings were different depending on the type of electric field applied. AC-EPD applied for not more than 5 min led to smooth films without bubble formation, while DC-EPD for 1 min or more showed deposits with microstructural defects possibly as result of water electrolysis. AC-EPD was thus for the first time demonstrated to be a suitable technique to deposit organic-inorganic composite coatings from aqueous suspensions, showing that applying a square wave and frequency of 1 kHz leads to uniform PAA-TiO(2) composite coatings on conductive materials.

  3. Organobentonites as multifunctional adsorbents of organic and inorganic water pollutants

    Directory of Open Access Journals (Sweden)

    Jović-Jovičić Natаša

    2014-01-01

    Full Text Available The aim of this study was to find a low cost, easy to synthesize and efficient adsorbent for the simultaneous adsorption of both organic and inorganic pollutants (including textile dyes, toxic metals etc.. The starting material, domestic bentonite clay from Bogovina was modified with amounts of hexadecyltrimethylammonium cations corresponding to 0.5 and 1.0 times of the value of the cation exchange capacity value. The organobentonites were tested as adsorbents in a three-dye-containing solution, a three-component solution of Pb2+, Cd2+ and Ni2+ and a hexa- component solution containing all investigated dyes and toxic metal cations. The used adsorbents showed the highest affinity toward Acid Yellow 99 and Ni2+ ions. Dye adsorption was enhanced in the presence of toxic metal cations, while the adsorption of all toxic cations from the hexa-component solution was lower than from the three-component solution containing only toxic cations. The synthesized hexadecyltrimethylammonium bentonite could be regarded as an efficient multifunctional adsorbent for the investigated type of water pollutants.

  4. In situ spectrophotometric measurement of dissolved inorganic carbon in seawater

    Science.gov (United States)

    Liua, Xuewu; Byrne, Robert H.; Adornato, Lori; Yates, Kimberly K.; Kaltenbacher, Eric; Ding, Xiaoling; Yang, Bo

    2013-01-01

    Autonomous in situ sensors are needed to document the effects of today’s rapid ocean uptake of atmospheric carbon dioxide (e.g., ocean acidification). General environmental conditions (e.g., biofouling, turbidity) and carbon-specific conditions (e.g., wide diel variations) present significant challenges to acquiring long-term measurements of dissolved inorganic carbon (DIC) with satisfactory accuracy and resolution. SEAS-DIC is a new in situ instrument designed to provide calibrated, high-frequency, long-term measurements of DIC in marine and fresh waters. Sample water is first acidified to convert all DIC to carbon dioxide (CO2). The sample and a known reagent solution are then equilibrated across a gas-permeable membrane. Spectrophotometric measurement of reagent pH can thereby determine the sample DIC over a wide dynamic range, with inherent calibration provided by the pH indicator’s molecular characteristics. Field trials indicate that SEAS-DIC performs well in biofouling and turbid waters, with a DIC accuracy and precision of ∼2 μmol kg–1 and a measurement rate of approximately once per minute. The acidic reagent protects the sensor cell from biofouling, and the gas-permeable membrane excludes particulates from the optical path. This instrument, the first spectrophotometric system capable of automated in situ DIC measurements, positions DIC to become a key parameter for in situ CO2-system characterizations.

  5. In situ spectrophotometric measurement of dissolved inorganic carbon in seawater.

    Science.gov (United States)

    Liu, Xuewu; Byrne, Robert H; Adornato, Lori; Yates, Kimberly K; Kaltenbacher, Eric; Ding, Xiaoling; Yang, Bo

    2013-10-01

    Autonomous in situ sensors are needed to document the effects of today's rapid ocean uptake of atmospheric carbon dioxide (e.g., ocean acidification). General environmental conditions (e.g., biofouling, turbidity) and carbon-specific conditions (e.g., wide diel variations) present significant challenges to acquiring long-term measurements of dissolved inorganic carbon (DIC) with satisfactory accuracy and resolution. SEAS-DIC is a new in situ instrument designed to provide calibrated, high-frequency, long-term measurements of DIC in marine and fresh waters. Sample water is first acidified to convert all DIC to carbon dioxide (CO2). The sample and a known reagent solution are then equilibrated across a gas-permeable membrane. Spectrophotometric measurement of reagent pH can thereby determine the sample DIC over a wide dynamic range, with inherent calibration provided by the pH indicator's molecular characteristics. Field trials indicate that SEAS-DIC performs well in biofouling and turbid waters, with a DIC accuracy and precision of ∼2 μmol kg(-1) and a measurement rate of approximately once per minute. The acidic reagent protects the sensor cell from biofouling, and the gas-permeable membrane excludes particulates from the optical path. This instrument, the first spectrophotometric system capable of automated in situ DIC measurements, positions DIC to become a key parameter for in situ CO2-system characterizations.

  6. Inorganic nanoparticles engineered to attack bacteria.

    Science.gov (United States)

    Miller, Kristen P; Wang, Lei; Benicewicz, Brian C; Decho, Alan W

    2015-11-01

    Antibiotics were once the golden bullet to constrain infectious bacteria. However, the rapid and continuing emergence of antibiotic resistance (AR) among infectious microbial pathogens has questioned the future utility of antibiotics. This dilemma has recently fueled the marriage of the disparate fields of nanochemistry and antibiotics. Nanoparticles and other types of nanomaterials have been extensively developed for drug delivery to eukaryotic cells. However, bacteria have very different cellular architectures than eukaryotic cells. This review addresses the chemistry of nanoparticle-based antibiotic carriers, and how their technical capabilities are now being re-engineered to attack, kill, but also non-lethally manipulate the physiologies of bacteria. This review also discusses the surface functionalization of inorganic nanoparticles with small ligand molecules, polymers, and charged moieties to achieve drug loading and controllable release.

  7. Scintillation response of organic and inorganic scintillators

    CERN Document Server

    Papadopoulos, L M

    1999-01-01

    A method to evaluate the scintillation response of organic and inorganic scintillators to different heavy ionizing particles is suggested. A function describing the rate of the energy consumed as fluorescence emission is derived, i.e., the differential response with respect to time. This function is then integrated for each ion and scintillator (anthracene, stilbene and CsI(Tl)) to determine scintillation response. The resulting scintillation responses are compared to the previously reported measured responses. Agreement to within 2.5% is observed when these data are normalized to each other. In addition, conclusions regarding the quenching parameter kB dependence on the type of the particle and the computed values of kB for certain ions are included. (author)

  8. Mechanisms of inorganic and organometallic reactions

    CERN Document Server

    The purpose of this series is to provide a continuing critical review of the literature concerned with mechanistic aspects of inorganic and organo­ metallic reactions in solution, with coverage being complete in each volume. The papers discussed are selected on the basis of relevance to the elucidation of reaction mechanisms and many include results of a nonkinetic nature when useful mechanistic information can be deduced. The period of literature covered by this volume is July 1982 through December 1983, and in some instances papers not available for inclusion in the previous volume are also included. Numerical results are usually reported in the units used by the original authors, except where data from different papers are com­ pared and conversion to common units is necessary. As in previous volumes material included covers the major areas of redox processes, reactions of the nonmetallic elements, reaction of inert and labile metal complexes and the reactions of organometallic compounds. While m...

  9. Ion conducting organic/inorganic hybrid polymers

    Science.gov (United States)

    Meador, Maryann B. (Inventor); Kinder, James D. (Inventor)

    2010-01-01

    This invention relates to a series of organic/inorganic hybrid polymers that are easy to fabricate into dimensionally stable films with good ion-conductivity over a wide range of temperatures for use in a variety of applications. The polymers are prepared by the reaction of amines, preferably diamines and mixtures thereof with monoamines with epoxy-functionalized alkoxysilanes. The products of the reaction are polymerized by hydrolysis of the alkoxysilane groups to produce an organic-containing silica network. Suitable functionality introduced into the amine and alkoxysilane groups produce solid polymeric membranes which conduct ions for use in fuel cells, high-performance solid state batteries, chemical sensors, electrochemical capacitors, electro-chromic windows or displays, analog memory devices and the like.

  10. Practical approaches to biological inorganic chemistry

    CERN Document Server

    Louro, Ricardo O

    2012-01-01

    The book reviews the use of spectroscopic and related methods to investigate the complex structures and mechanisms of biological inorganic systems that contain metals. Each chapter presents an overview of the technique including relevant theory, clearly explains what it is and how it works and then presents how the technique is actually used to evaluate biological structures. Practical examples and problems are included to illustrate each technique and to aid understanding. Designed for students and researchers who want to learn both the basics, and more advanced aspects of bioinorganic chemistry. It includes many colour illustrations enable easier visualization of molecular mechanisms and structures. It provides worked examples and problems that are included to illustrate and test the reader's understanding of each technique. It is written by a multi-author team who use and teach the most important techniques used today to analyse complex biological structures.

  11. Inorganic photocatalysts for overall water splitting.

    Science.gov (United States)

    Xing, Jun; Fang, Wen Qi; Zhao, Hui Jun; Yang, Hua Gui

    2012-04-01

    Photocatalytic water splitting using semiconductor photocatalysts has been considered as a "green" process for converting solar energy into hydrogen. The pioneering work on electrochemical photolysis of water at TiO(2) electrode, reported by Fujishima and Honda in 1972, ushered in the area of solar fuel. As the real ultimate solution for solar fuel-generation, overall water splitting has attracted interest from researchers for some time, and a variety of inorganic photocatalysts have been developed to meet the challenge of this dream reaction. To date, high-efficiency hydrogen production from pure water without the assistance of sacrificial reagents remains an open challenge. In this Focus Review, we aim to provide a whole picture of overall water splitting and give an outlook for future research.

  12. Recent trends in inorganic mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Smith, D.H.; Barshick, C.M.; Duckworth, D.C.; Riciputi, L.R.

    1996-10-01

    The field of inorganic mass spectrometry has seen substantial change in the author`s professional lifetime (over 30 years). Techniques in their infancy 30 years ago have matured; some have almost disappeared. New and previously unthought of techniques have come into being; some of these, such as ICP-MS, are reasonably mature now, while others have some distance to go before they can be so considered. Most of these new areas provide fertile fields for researchers, both in the development of new analytical techniques and by allowing fundamental studies to be undertaken that were previously difficult, impossible, or completely unforeseen. As full coverage of the field is manifestly impossible within the framework of this paper, only those areas with which the author has personal contact will be discussed. Most of the work originated in his own laboratory, but that of other laboratories is covered where it seemed appropriate.

  13. Simulation of perovskite solar cells with inorganic hole transporting materials

    DEFF Research Database (Denmark)

    Wang, Yan; Xia, Zhonggao; Liu, Yiming

    2015-01-01

    Device modeling organolead halide perovskite solar cells with planar architecture based on inorganic hole transporting materials (HTMs) were performed. A thorough understanding of the role of the inorganic HTMs and the effect of band offset between HTM/absorber layers is indispensable for further...

  14. Inorganic Analyses in Water Quality Control Programs. Training Manual.

    Science.gov (United States)

    Kroner, Audrey; And Others

    This lecture/laboratory manual for a five-day course deals with the analysis of selected inorganic pollutants. The manual is an instructional aid for classroom presentations to those with little or no experience in the field, but having one year (or equivalent) of college level inorganic chemistry, one semester of college level quantitative…

  15. Organometallic-inorganic hybrid electrodes for lithium-ion batteries

    Science.gov (United States)

    Huang, Qian; Lemmon, John P.; Choi, Daiwon; Cosimbescu, Lelia

    2016-09-13

    Disclosed are embodiments of active materials for organometallic and organometallic-inorganic hybrid electrodes and particularly active materials for organometallic and organometallic-inorganic hybrid cathodes for lithium-ion batteries. In certain embodiments the organometallic material comprises a ferrocene polymer.

  16. Optical Waveguides from Organic/Inorganic Hybrid Materials

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Organic/inorganic material has attracted great attentions because its importance as photonic materials. We report on our recent results on organic/inorganic hybrid sol-gel materials and optical waveguides like splitter, thermo-optic switch and micro-cavity laser.

  17. Optical Waveguides from Organic/Inorganic Hybrid Materials

    Institute of Scientific and Technical Information of China (English)

    Liying Liu; Lei Xu; Wencheng Wang

    2003-01-01

    Organic/inorganic material has attracted great attentions because its importance as photonic materials. We report on our recent results on organic/inorganic hybrid sol-gel materials and optical waveguides like splitter,thermo-optic switch and micro-cavity laser.

  18. Computer information resources of inorganic chemistry and materials science

    Energy Technology Data Exchange (ETDEWEB)

    Kiselyova, N N; Dudarev, V A; Zemskov, V S [A.A.Baikov Institute of Metallurgy and Materials Science, Russian Academy of Sciences, Moscow (Russian Federation)

    2010-02-28

    Information systems used in inorganic chemistry and materials science are considered. The following basic trends in the development of modern information systems in these areas are highlighted: access to information via the Internet, merging of documental and factual databases, involvement of experts in the evaluation of the data reliability, supplementing databases with information analysis tools on the properties of inorganic substances and materials.

  19. Synthesis of Porous Inorganic Hollow Fibers without Harmful Solvents

    NARCIS (Netherlands)

    Shukla, S.; Wit, de Patrick; Luiten-Olieman, Mieke W.J.; Kappert, Emiel J.; Nijmeijer, Arian; Benes, Nieck E.

    2015-01-01

    A route for the fabrication of porous inorganic hollow fibers with high surface-area-to-volume ratio that avoids harmful solvents is presented. The approach is based on bio-ionic gelation of an aqueous mixture of inorganic particles and sodium alginate during wet spinning. In a subsequent thermal tr

  20. A combined particle trap/HTDMA hygroscopicity study of mixed inorganic/organic aerosol particles

    Science.gov (United States)

    Zardini, A. A.; Sjogren, S.; Marcolli, C.; Krieger, U. K.; Gysel, M.; Weingartner, E.; Baltensperger, U.; Peter, T.

    2008-09-01

    Atmospheric aerosols are often mixtures of inorganic and organic material. Organics can represent a large fraction of the total aerosol mass and are comprised of water-soluble and insoluble compounds. Increasing attention was paid in the last decade to the capability of mixed inorganic/organic aerosol particles to take up water (hygroscopicity). We performed hygroscopicity measurements of internally mixed particles containing ammonium sulfate and carboxylic acids (citric, glutaric, adipic acid) in parallel with an electrodynamic balance (EDB) and a hygroscopicity tandem differential mobility analyzer (HTDMA). The organic compounds were chosen to represent three distinct physical states. During hygroscopicity cycles covering hydration and dehydration measured by the EDB and the HTDMA, pure citric acid remained always liquid, adipic acid remained always solid, while glutaric acid could be either. We show that the hygroscopicity of mixtures of the above compounds is well described by the Zdanovskii-Stokes-Robinson (ZSR) relationship as long as the two-component particle is completely liquid in the ammonium sulfate/glutaric acid system; deviations up to 10% in mass growth factor (corresponding to deviations up to 3.5% in size growth factor) are observed for the ammonium sulfate/citric acid 1:1 mixture at 80% RH. We observe even more significant discrepancies compared to what is expected from bulk thermodynamics when a solid component is present. We explain this in terms of a complex morphology resulting from the crystallization process leading to veins, pores, and grain boundaries which allow for water sorption in excess of bulk thermodynamic predictions caused by the inverse Kelvin effect on concave surfaces.

  1. Transport of inorganic compounds through compacted clay

    Energy Technology Data Exchange (ETDEWEB)

    Liao, W.P.

    1989-01-01

    Compacted clay liners are widely utilized as leachate barrier in landfills for waste. The main purpose of this research was to study the transport of inorganic compounds through compacted clay. The subjects of interest included the diffusional migration of chemicals at low flow rates, the effective porosity of fine-grained soils, the transport of solutes in unsaturated clays, and the effect of adsorption processes on the transport of reactive solutes. Two clay soils, kaolinite and Lufkin clay, were used in the laboratory column tests and subjected to constant hydraulic gradients of 1 to 50. Inorganic tracers (Cl{sup {minus}} Br{sup {minus}}, K{sup +}, and Zn{sup 2+}) were added to the permeating water as a step input. Conclusions are: (a) the experimental data from soil specimens subjected to various gradients showed that diffusional transport did affect the migration of the tracers in fine-grained media. At low gradients, hydrodynamic dispersion was almost solely related to molecular diffusion rather than mechanical mixing; (b) the breakthrough curves for kaolinite specimens showed that the ratios of effective porosity to total porosity were 0.25 to 1.0. The effect of low effective porosity on transport of the tracers was much greater than that of diffusion; (c) the soils that were not presoaked before tracers were introduced had lower effective porosity and greater dispersion of solutes that did the presoaked soils; (d) no evidence of the existence of a threshold gradient was observed; and (e) the retardation factors predicted from batch equilibrium tests matched the results from column tests poorly, probably due to hydrodynamic effects or geochemical differences between the two soil/solution systems.

  2. Efficient Organic/Inorganic Hybrid Solar Cell Integrating Polymer Nanowires and Inorganic Nanotetrapods

    Science.gov (United States)

    Xu, Weizhe; Tan, Furui; Liu, Xiansheng; Zhang, Weifeng; Qu, Shengchun; Wang, Zhijie; Wang, Zhanguo

    2017-01-01

    Constructing a highly efficient bulk-heterojunction is of critical importance to the hybrid organic/inorganic solar cells. Here in this work, we introduce a novel hybrid architecture containing P3HT nanowire and CdSe nanotetrapod as bicontinuous charge channels for holes and electrons, respectively. Compared to the traditionally applied P3HT molecules, the well crystallized P3HT nanowires qualify an enhanced light absorption at the long wavelength as well as strengthened charge carrier transport in the hybrid active layer. Accordingly, based on efficient dissociation of photogenerated excitons, the interpercolation of these two nano-building blocks allows a photovoltaic conversion efficiency of 1.7% in the hybrid solar cell, up to 42% enhancement compared to the reference solar cell with traditional P3HT molecules as electron donor. Our work provides a promising hybrid structure for efficient organic/inorganic bulk-heterojunction solar cells.

  3. Efficient Organic/Inorganic Hybrid Solar Cell Integrating Polymer Nanowires and Inorganic Nanotetrapods.

    Science.gov (United States)

    Xu, Weizhe; Tan, Furui; Liu, Xiansheng; Zhang, Weifeng; Qu, Shengchun; Wang, Zhijie; Wang, Zhanguo

    2017-12-01

    Constructing a highly efficient bulk-heterojunction is of critical importance to the hybrid organic/inorganic solar cells. Here in this work, we introduce a novel hybrid architecture containing P3HT nanowire and CdSe nanotetrapod as bicontinuous charge channels for holes and electrons, respectively. Compared to the traditionally applied P3HT molecules, the well crystallized P3HT nanowires qualify an enhanced light absorption at the long wavelength as well as strengthened charge carrier transport in the hybrid active layer. Accordingly, based on efficient dissociation of photogenerated excitons, the interpercolation of these two nano-building blocks allows a photovoltaic conversion efficiency of 1.7% in the hybrid solar cell, up to 42% enhancement compared to the reference solar cell with traditional P3HT molecules as electron donor. Our work provides a promising hybrid structure for efficient organic/inorganic bulk-heterojunction solar cells.

  4. Organic-inorganic interface-induced multi-fluorescence of MgO nanocrystal clusters and their applications in cellular imaging.

    Science.gov (United States)

    Xie, Shuifen; Bao, Shixiong; Ouyang, Junjie; Zhou, Xi; Kuang, Qin; Xie, Zhaoxiong; Zheng, Lansun

    2014-04-25

    Surface functionalization of inorganic nanomaterials through chemical binding of organic ligands on the surface unsaturated atoms, forming unique organic-inorganic interfaces, is a powerful approach for creating special functions for inorganic nanomaterials. Herein, we report the synthesis of hierarchical MgO nanocrystal clusters (NCs) with an organic-inorganic interface induced multi-fluorescence and their application as new alternative labels for cellular imaging. The synthetic method was established by a dissolution and regrowth process with the assistance of carboxylic acid, in which the as-prepared MgO NCs were modified with carboxylic groups at the coordinatively unsaturated atoms of the surface. By introducing acetic acid to partially replace oleic acid in the reaction, the optical absorption of the produced MgO NCs was progressively engineered from the UV to the visible region. Importantly, with wider and continuous absorption profile, those MgO NCs presented bright and tunable multicolor emissions from blue-violet to green and yellow, with the highest absolute quantum yield up to (33±1) %. The overlap for the energy levels of the inorganic-organic interface and low-coordinated states stimulated a unique fluorescence resonance energy transfer phenomenon. Considering the potential application in cellular imaging, such multi-fluorescent MgO NCs were further encapsulated with a silica shell to improve the water solubility and stability. As expected, the as-formed MgO@SiO2 NCs possessed great biocompatibility and high performance in cellular imaging.

  5. In-Depth Coursework in Undergraduate Inorganic Chemistry: Results from a National Survey of Inorganic Chemistry Faculty

    Science.gov (United States)

    Raker, Jeffrey R.; Reisner, Barbara A.; Smith, Sheila R.; Stewart, Joanne L.; Crane, Johanna L.; Pesterfield, Les; Sobel, Sabrina G.

    2015-01-01

    A national survey of inorganic chemists explored the self-reported topics covered in in-depth inorganic chemistry courses at the postsecondary level; an in-depth course is defined by the American Chemical Society's Committee on Professional Training as a course that integrates and covers topics that were introduced in introductory and foundation…

  6. Preparation of new hybrid organic/inorganic polymeric chiral stationary phases for ligand-exchange chromatography

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Three new hybrid organic/inorganic polymeric ligand-exchange chiral stationary phases were developed by radical chain transfer reaction and surface grafting on silica gel, and successfully used for the enantioseparations of DL-amino acids and DL-hydroxyl acids. The resolutions were achieved by using water containing 2.0 × 10-4 mol/L of CuAc2 as a mobile phase, column temperature of 40 ℃, flow rate of 1.0 mL/min and detection at UV 254 mn. The elution order of D-isomer before L-isomer was observed for all DL-amino acids resolved except DL-Pro.

  7. Thermodynamic Modeling of Organic-Inorganic Aerosols with the Group-Contribution Model AIOMFAC

    Science.gov (United States)

    Zuend, A.; Marcolli, C.; Luo, B. P.; Peter, T.

    2009-04-01

    Liquid aerosol particles are - from a physicochemical viewpoint - mixtures of inorganic salts, acids, water and a large variety of organic compounds (Rogge et al., 1993; Zhang et al., 2007). Molecular interactions between these aerosol components lead to deviations from ideal thermodynamic behavior. Strong non-ideality between organics and dissolved ions may influence the aerosol phases at equilibrium by means of liquid-liquid phase separations into a mainly polar (aqueous) and a less polar (organic) phase. A number of activity models exists to successfully describe the thermodynamic equilibrium of aqueous electrolyte solutions. However, the large number of different, often multi-functional, organic compounds in mixed organic-inorganic particles is a challenging problem for the development of thermodynamic models. The group-contribution concept as introduced in the UNIFAC model by Fredenslund et al. (1975), is a practical method to handle this difficulty and to add a certain predictability for unknown organic substances. We present the group-contribution model AIOMFAC (Aerosol Inorganic-Organic Mixtures Functional groups Activity Coefficients), which explicitly accounts for molecular interactions between solution constituents, both organic and inorganic, to calculate activities, chemical potentials and the total Gibbs energy of mixed systems (Zuend et al., 2008). This model enables the computation of vapor-liquid (VLE), liquid-liquid (LLE) and solid-liquid (SLE) equilibria within one framework. Focusing on atmospheric applications we considered eight different cations, five anions and a wide range of alcohols/polyols as organic compounds. With AIOMFAC, the activities of the components within an aqueous electrolyte solution are very well represented up to high ionic strength. We show that the semi-empirical middle-range parametrization of direct organic-inorganic interactions in alcohol-water-salt solutions enables accurate computations of vapor-liquid and liquid

  8. Inorganic nanoparticles for transfection of mammalian cells and removal of viruses from aqueous solutions.

    Science.gov (United States)

    Link, Nils; Brunner, Tobias J; Dreesen, Imke A J; Stark, Wendelin J; Fussenegger, Martin

    2007-12-01

    Owing to their small size, synthetic nanoparticles show unprecedented biophysical and biochemical properties which may foster novel advances in life-science research. Using flame-spray synthesis technology we have produced non-coated aluminum-, calcium-, cerium-, and zirconium-derived inorganic metal oxide nanoparticles which not only exhibit high affinity for nucleic acids, but can sequester such compounds from aqueous solution. This non-covalent DNA-binding capacity was successfully used to transiently transfect a variety of mammalian cells including human, reaching transfection efficiencies which compared favorably with classic calcium phosphate precipitation (CaP) procedures and lipofection. In this straightforward protocol, transfection was enabled by simply mixing nanoparticles with DNA in solution prior to addition to the target cell population. Transiently transfected cells showed higher production levels of the human secreted glycoprotein SEAP compared to isogenic populations transfected with established technologies. Inorganic metal oxide nanoparticles also showed a high binding capacity to human-pathogenic viruses including adenovirus, adeno-associated virus and human immunodeficiency virus type 1 and were able to clear these pathogens from aqueous solutions. The DNA transfection and viral clearance capacities of inorganic metal oxide nanoparticles may provide cost-effective biopharmaceutical manufacturing and water treatment in developing countries.

  9. Organic and inorganic dietary phosphorus and its management in chronic kidney disease.

    Science.gov (United States)

    Noori, Nazanin; Sims, John J; Kopple, Joel D; Shah, Anuja; Colman, Sara; Shinaberger, Christian S; Bross, Rachelle; Mehrotra, Rajnish; Kovesdy, Csaba P; Kalantar-Zadeh, Kamyar

    2010-04-01

    Dietary phosphorus control is often a main strategy in the management of patients with chronic kidney disease. Dietary protein is a major source of phosphorus intake. Recent data indicate that imposed dietary phosphorus restriction may compromise the need for adequate protein intake, leading to protein-energy wasting and possibly to increased mortality. The two main sources of dietary phosphorus are organic, including animal and vegetarian proteins, and inorganic, mostly food preservatives. Animal-based foods and plant are abundant in organic phosphorus. Usually 40% to 60% of animal-based phosphorus is absorbed; this varies by degree of gastrointestinal vitamin-D-receptor activation, whereas plant phosphorus, mostly associated with phytates, is less absorbable by human gastrointestinal tract. Up to 100% of inorganic phosphorus in processed foods may be absorbed; ie, phosphorus in processed cheese and some soda (cola) drinks. A recent study suggests that a higher dietary phosphorus-protein intake ratio is associated with incremental death risk in patients on long-term hemodialysis. Hence, for phosphorus management in chronic kidney disease, in addition to absolute dietary phosphorus content, the chemical structure (inorganic versus organic), type (animal versus plant), and phosphorus-protein ratio should be considered. We recommend foods and supplements with no or lowest quantity of inorganic phosphorus additives, more plant-based proteins, and a dietary phosphorus-protein ratio of less than 10 mg/g. Fresh (nonprocessed) egg white (phosphorus-protein ratio less than 2 mg/g) is a good example of desirable food, which contains a high proportion of essential amino acids with low amounts of fat, cholesterol, and phosphorus.

  10. A thermodynamic model of mixed organic-inorganic aerosols to predict activity coefficients

    Directory of Open Access Journals (Sweden)

    A. Zuend

    2008-03-01

    Full Text Available Tropospheric aerosols contain mixtures of inorganic salts, acids, water, and a large variety of organic compounds. Interactions between these substances in liquid mixtures lead to discrepancies from ideal thermodynamic behaviour. By means of activity coefficients, non-ideal behaviour can be taken into account. We present here a thermodynamic model named AIOMFAC (Aerosol Inorganic–Organic Mixtures Functional groups Activity Coefficients that is able to calculate activity coefficients covering inorganic, organic, and organic–inorganic interactions in aqueous solutions over a wide concentration range. This model is based on the activity coefficient model LIFAC by Yan et al. (1999 that we modified and reparametrised to better describe atmospherically relevant conditions and mixture compositions. Focusing on atmospheric applications we considered H+, Li+, Na+, K+, NH4+, Mg2+, Ca2+, Cl, Br, NO3, HSO4, and SO42− as cations and anions and a wide range of alcohols/polyols composed of the functional groups CHn and OH as organic compounds. With AIOMFAC, the activities of the components within an aqueous electrolyte solution are well represented up to high ionic strength. Most notably, a semi-empirical middle-range parametrisation of direct organic–inorganic interactions in alcohol + water + salt solutions strongly improves the agreement between experimental and modelled activity coefficients. At room temperature, this novel thermodynamic model offers the possibility to compute equilibrium relative humidities, gas/particle partitioning and liquid–liquid phase separations with high accuracy. In further studies, other organic functional groups will be introduced. The model framework is not restricted to specific ions or organic compounds and is therefore

  11. Influence of Aqueous Inorganic Anions on the Reactivity of Nanoparticles in TiO2 Photocatalysis.

    Science.gov (United States)

    Farner Budarz, Jeffrey; Turolla, Andrea; Piasecki, Aleksander F; Bottero, Jean-Yves; Antonelli, Manuela; Wiesner, Mark R

    2017-03-21

    The influence of inorganic anions on the photoreactivity and aggregation of titanium dioxide nanoparticles (NPs) was assessed by dosing carbonate, chloride, nitrate, phosphate, and sulfate as potassium salts at multiple concentrations. NP stability was monitored in terms of aggregate morphology and electrophoretic mobility (EPM). Aggregate size and fractal dimension were measured over time by laser diffraction, and the isoelectric point (IEP) as a function of anion and concentration was obtained by measuring EPM versus pH. Phosphate, carbonate, and to a lesser extent, sulfate decreased the IEP of TiO2 and stabilized NP suspensions owing to specific surface interactions, whereas this was not observed for nitrate and chloride. TiO2 NPs were exposed to UV-A radiation, and the photoreactivity was assessed by monitoring the production of reactive species over time both at the NP surface (photogenerated holes) and in the bulk solution (hydroxyl radicals) by observing their reactions with the selective probe compounds iodide and terephthalic acid, respectively. The generation of photogenerated holes and hydroxyl radicals was influenced by each inorganic anion to varying degrees. Carbonate and phosphate inhibited the oxidation of iodide, and this interaction was successfully described by a Langmuir-Hinshelwood mechanism and related to the characteristics of TiO2 aggregates. Chloride and nitrate do not specifically interact with TiO2, and sulfate creates relatively weak interactions with the TiO2 surface such that no decrease in photogenerated hole reactivity was observed. A decrease in hydroxyl radical generation was observed for all inorganic anions. Quenching rate constants for the reaction of hydroxyl radicals with each inorganic anion do not provide a comprehensive explanation for the magnitude of this decrease, which arises from the interplay of several physicochemical phenomena. This work shows that the reactivity of NPs will be strongly influenced by the makeup of

  12. First implementation of secondary inorganic aerosols in the MOCAGE version R2.15.0 chemistry transport model

    Science.gov (United States)

    Guth, J.; Josse, B.; Marécal, V.; Joly, M.; Hamer, P.

    2016-01-01

    In this study we develop a secondary inorganic aerosol (SIA) module for the MOCAGE chemistry transport model developed at CNRM. The aim is to have a module suitable for running at different model resolutions and for operational applications with reasonable computing times. Based on the ISORROPIA II thermodynamic equilibrium module, the new version of the model is presented and evaluated at both the global and regional scales. The results show high concentrations of secondary inorganic aerosols in the most polluted regions: Europe, Asia and the eastern part of North America. Asia shows higher sulfate concentrations than other regions thanks to emission reductions in Europe and North America. Using two simulations, one with and the other without secondary inorganic aerosol formation, the global model outputs are compared to previous studies, to MODIS AOD retrievals, and also to in situ measurements from the HTAP database. The model shows a better agreement with MODIS AOD retrievals in all geographical regions after introducing the new SIA scheme. It also provides a good statistical agreement with in situ measurements of secondary inorganic aerosol composition: sulfate, nitrate and ammonium. In addition, the simulation with SIA generally gives a better agreement with observations for secondary inorganic aerosol precursors (nitric acid, sulfur dioxide, ammonia), in particular with a reduction of the modified normalized mean bias (MNMB). At the regional scale, over Europe, the model simulation with SIA is compared to the in situ measurements from the EMEP database and shows a good agreement with secondary inorganic aerosol composition. The results at the regional scale are consistent with those obtained from the global simulations. The AIRBASE database was used to compare the model to regulated air quality pollutants: particulate matter, ozone and nitrogen dioxide concentrations. Introduction of the SIA in MOCAGE provides a reduction in the PM2.5 MNMB of 0.44 on a

  13. Descriptive Inorganic Chemistry (by Geoff Rayner-Canham)

    Science.gov (United States)

    Rabinovich, Daniel

    1998-06-01

    Geoff Rayner-Canham. W. H. Freeman: New York, 1996. 492 pp. ISBN: 0-7167-2819-2. $67.95. There are plenty of good inorganic chemistry books on the market, from venerable reference works (e.g., Cotton and Wilkinson's Advanced Inorganic Chemistry, Greenwood and Earnshaw's Chemistry of the Elements) to "comprehensive" two-semester textbooks (e.g., Huheey, Keiter, and Keiter's Inorganic Chemistry: Principles of Structure and Reactivity, Douglas, McDaniel, and Alexander's Concepts and Models of Inorganic Chemistry). Undergraduate students, especially those new to inorganic chemistry, frequently find these books overwhelming in depth and length (not to mention weight!). Alternatively, some shorter books with less ambitious goals present an oversimplified view of the field or sacrifice conceptual material on behalf of sections on environmental, industrial, or biological chemistry. Rayner-Canham's Descriptive Inorganic Chemistry, a one-semester book aimed specifically at the introductory (sophomore) level, provides an excellent balance of theory and descriptive material, with a fresh look at traditional and current areas of interest in inorganic chemistry.

  14. Inorganic nanolayers: structure, preparation, and biomedical applications

    Directory of Open Access Journals (Sweden)

    Saifullah B

    2015-09-01

    Full Text Available Bullo Saifullah, Mohd Zobir B HusseinMaterials Synthesis and Characterization Laboratory, Institute of Advanced Technology (ITMA, Universiti Putra Malaysia, Serdang, MalaysiaAbstract: Hydrotalcite-like compounds are two-dimensional inorganic nanolayers also known as clay minerals or anionic clays or layered double hydroxides/layered hydroxy salts, and have emerged as a single type of material with numerous biomedical applications, such as drug delivery, gene delivery, cosmetics, and biosensing. Inorganic nanolayers are promising materials due to their fascinating properties, such as ease of preparation, ability to intercalate different type of anions (inorganic, organic, biomolecules, and even genes, high thermal stability, delivery of intercalated anions in a sustained manner, high biocompatibility, and easy biodegradation. Inorganic nanolayers have been the focus for researchers over the last decade, resulting in widening application horizons, especially in the field of biomedical science. These nanolayers have been widely applied in drug and gene delivery. They have also been applied in biosensing technology, and most recently in bioimaging science. The suitability of inorganic nanolayers for application in drug delivery, gene delivery, biosensing technology, and bioimaging science makes them ideal materials to be applied for theranostic purposes. In this paper, we review the structure, methods of preparation, and latest advances made by inorganic nanolayers in such biomedical applications as drug delivery, gene delivery, biosensing, and bioimaging.Keywords: inorganic nanolayers, layered double hydroxides, layered hydroxy salts, drug delivery, biosensors, bioimaging

  15. Research and development of hydrogen separation technology with inorganic membranes

    Energy Technology Data Exchange (ETDEWEB)

    Fain, D.E.

    1999-07-01

    Inorganic membrane technology has long been expected to provide new economical methods for industrial and waste management processes. At this time, the only commercially valuable inorganic membranes are the ultra filters derived from the French process that was used to produce the barrier for the French Gaseous Diffusion Plants. But these membranes are very expensive and have limited areas of application. Over the past fifteen years, scientists now in the Inorganic Membrane Technology Laboratory (IMTL) in Oak Ridge, Tennessee have developed theories and processes for inorganic membranes that can be used to design and produce inorganic membranes for a very broad range of applications. A part of the fabrication process is an adaptive spinoff from the still classified process used to manufacture barriers for the U.S. Gaseous Diffusion Process. Although that part of the process is classified, it is a very flexible and adaptable process and it can be used with a broad range of materials. With the theories and design capabilities developed in the last fifteen years, this new adaptive manufacturing technology can be used to manufacture commercial inorganic membranes that are not useful for the separation of uranium isotopes and they have little or no relation to the barriers that were used to separate uranium isotopes. The development and deployment of such inorganic membranes can be very beneficial to U.S. industry. Inorganic membranes can be specifically designed and manufactured for a large number of different applications. Such membranes can greatly improve the efficiency of a broad range of industrial processes and provide new technology for waste management. These inorganic membranes have the potential for major energy savings and conservation of energy. They can provide the means for significant improvements in the competitiveness of US Industry and improve the economy and health and welfare of the nation.

  16. Teaching Chemistry in the New Century: Inorganic Chemistry

    Science.gov (United States)

    Dorhout, Peter K.

    2001-09-01

    At the San Diego ACS meeting, members of the academic community came together to share their visions for teaching inorganic chemistry. They discussed new laboratory experiences, virtual textbooks, integration of computers in the laboratory, undergraduate research experiences, and new ways of classifying reactions to enable students to recognize and categorize reaction types. It was clear from the presentations that, while the toolbox of the inorganic chemist is not now as sophisticated as the organic chemist's, that toolbox must evolve (and is evolving) if we are to understand just a fraction of the unique chemistry that is inorganic.

  17. Sol-gel processing with inorganic metal salt precursors

    Science.gov (United States)

    Hu, Zhong-Cheng

    2004-10-19

    Methods for sol-gel processing that generally involve mixing together an inorganic metal salt, water, and a water miscible alcohol or other organic solvent, at room temperature with a macromolecular dispersant material, such as hydroxypropyl cellulose (HPC) added. The resulting homogenous solution is incubated at a desired temperature and time to result in a desired product. The methods enable production of high quality sols and gels at lower temperatures than standard methods. The methods enable production of nanosize sols from inorganic metal salts. The methods offer sol-gel processing from inorganic metal salts.

  18. Nanoscale Organic−Inorganic Hybrid Lubricants

    KAUST Repository

    Kim, Daniel

    2011-03-15

    Silica (SiO2) nanoparticles densely grafted with amphiphilic organic chains are used to create a family of organic-inorganic hybrid lubricants. Short sulfonate-functionalized alkylaryl chains covalently tethered to the particles form a dense corona brush that stabilizes them against aggregation. When these hybrid particles are dispersed in poly-α-olefin (PAO) oligomers, they form homogeneous nanocomposite fluids at both low and high particle loadings. By varying the volume fraction of the SiO2 nanostructures in the PAO nanocomposites, we show that exceptionally stable hybrid lubricants can be created and that their mechanical properties can be tuned to span the spectrum from simple liquids to complex gels. We further show that these hybrid lubricants simultaneously exhibit lower interfacial friction coefficients, enhanced wear and mechanical properties, and superior thermal stability in comparison with either PAO or its nanocomposites created at low nanoparticle loadings. Profilometry and energy dispersive X-ray spectroscopic analysis of the wear track show that the enhanced wear characteristics in PAO-SiO2 composite lubricants originate from two sources: localization of the SiO2 particles into the wear track and extension of the elastohydrodynamic lubrication regime to Sommerfeld numbers more than an order of magnitude larger than for PAO. © 2011 American Chemical Society.

  19. Tuberculosis: An Inorganic Medicinal Chemistry Perspective.

    Science.gov (United States)

    Viganor, Livia; Skerry, Ciaran; McCann, Malachy; Devereux, Michael

    2015-01-01

    Tuberculosis (TB) which is caused by the resilient pathogen Mycobacterium tuberculosis (MTB) has re-emerged to become a leading public health problem in the world. The growing number of multi-drug resistant MTB strains and the more recently emerging problem with the extensively drug resistant strains of the pathogen are greatly undermining conventional anti-TB therapeutic strategies which are lengthy and expose patients to toxicity and other unwanted side effects. The search for new anti-TB drugs essentially involves either the repurposing of existing organic drugs which are now off patent and already FDA approved, the synthesis of modified analogues of existing organic drugs, with the aim of shortening and improving drug treatment for the disease, or the search for novel structures that offer the possibility of new mechanisms of action against the mycobacterium. Inorganic medicinal chemistry offers an alternative to organic drugs through opportunities for the design of therapeutics that target different biochemical pathways. The incorporation of metal ions into the molecular structure of a potential drug offers the medicinal chemist an opportunity to exploit structural diversity, have access to various oxidation states of the metal and also offer the possibility of enhancing the activity of an established organic drug through its coordination to the metal centre. In this review, we summarize what is currently known about the antitubercular capability of metal complexes, their mechanisms of action and speculate on their potential applications in the clinic.

  20. Plant cell proliferation inside an inorganic host.

    Science.gov (United States)

    Perullini, Mercedes; Rivero, María Mercedes; Jobbágy, Matías; Mentaberry, Alejandro; Bilmes, Sara A

    2007-01-10

    In recent years, much attention has been paid to plant cell culture as a tool for the production of secondary metabolites and the expression of recombinant proteins. Plant cell immobilization offers many advantages for biotechnological processes. However, the most extended matrices employed, such as calcium-alginate, cannot fully protect entrapped cells. Sol-gel chemistry of silicates has emerged as an outstanding strategy to obtain biomaterials in which living cells are truly protected. This field of research is rapidly developing and a large number of bacteria and yeast-entrapping ceramics have already been designed for different applications. But even mild thermal and chemical conditions employed in sol-gel synthesis may result harmful to cells of higher organisms. Here we present a method for the immobilization of plant cells that allows cell growth at cavities created inside a silica matrix. Plant cell proliferation was monitored for a 6-month period, at the end of which plant calli of more than 1 mm in diameter were observed inside the inorganic host. The resulting hybrid device had good mechanical stability and proved to be an effective barrier against biological contamination, suggesting that it could be employed for long-term plant cell entrapment applications.

  1. Infrared and Raman spectra of inorganic and coordination compounds theory and applications in inorganic chemistry

    CERN Document Server

    Nakamoto, Kazuo

    2008-01-01

    The Sixth Edition of this classic work comprises the most comprehensive and current guide to infrared and Raman spectra of inorganic, organometallic, bioinorganic, and coordination compounds. From fundamental theories of vibrational spectroscopy to applications in a variety of compound types, this has been extensively updated. New topics include the theoretical calculations of vibrational frequencies (DFT method), chemical synthesis by matrix co-condensation reactions, time-resolved Raman spectroscopy, and more. This volume is a core reference for chemists and medical professionals working with infrared or Raman spectroscopies and an excellent textbook for graduate courses.

  2. DNA-inorganic hybrid nanovaccine for cancer immunotherapy

    Science.gov (United States)

    Zhu, Guizhi; Liu, Yijing; Yang, Xiangyu; Kim, Young-Hwa; Zhang, Huimin; Jia, Rui; Liao, Hsien-Shun; Jin, Albert; Lin, Jing; Aronova, Maria; Leapman, Richard; Nie, Zhihong; Niu, Gang; Chen, Xiaoyuan

    2016-03-01

    Cancer evolves to evade or compromise the surveillance of the immune system, and cancer immunotherapy aims to harness the immune system in order to inhibit cancer development. Unmethylated CpG dinucleotide-containing oligonucleotides (CpG), a class of potent adjuvants that activate the toll-like receptor 9 (TLR9) located in the endolysosome of many antigen-presenting cells (APCs), are promising for cancer immunotherapy. However, clinical application of synthetic CpG confronts many challenges such as suboptimal delivery into APCs, unfavorable pharmacokinetics caused by limited biostability and short in vivo half-life, and side effects associated with leaking of CpG into the systemic circulation. Here we present DNA-inorganic hybrid nanovaccines (hNVs) for efficient uptake into APCs, prolonged tumor retention, and potent immunostimulation and cancer immunotherapy. hNVs were self-assembled from concatemer CpG analogs and magnesium pyrophosphate (Mg2PPi). Mg2PPi renders hNVs resistant to nuclease degradation and thermal denaturation, both of which are demanding characteristics for effective vaccination and the storage and transportation of vaccines. Fluorophore-labeled hNVs were tracked to be efficiently internalized into the endolysosomes of APCs, where Mg2PPi was dissolved in an acidic environment and thus CpG analogs were exposed to hNVs. Internalized hNVs in APCs led to (1) elevated secretion of proinflammatory factors, and (2) elevated expression of co-stimulatory factors. Compared with molecular CpG, hNVs dramatically prolonged the tissue retention of CpG analogs and reduced splenomegaly, a common side effect of CpG. In a melanoma mouse model, two injections of hNVs significantly inhibited the tumor growth and outperformed the molecular CpG. These results suggest hNVs are promising for cancer immunotherapy.Cancer evolves to evade or compromise the surveillance of the immune system, and cancer immunotherapy aims to harness the immune system in order to inhibit

  3. Effect of organic and inorganic forms of selenium in diets on turkey semen quality.

    Science.gov (United States)

    Slowińska, M; Jankowski, J; Dietrich, G J; Karol, H; Liszewska, E; Glogowski, J; Kozłowski, K; Sartowska, K; Ciereszko, A

    2011-01-01

    The effects of Se supplementation and its organic or inorganic form on semen quantitative parameters (ejaculate volume, sperm concentration, and total number of sperm) and biochemical parameters of seminal plasma (protein concentration, acid phosphatase activity, superoxide dismutase activity, and total antioxidant capacity) were investigated over a 25-wk reproductive season. Additionally, DNA fragmentation and motility characteristics of turkey spermatozoa were measured. The parameters of turkey semen in relation to yellow semen syndrome were also determined. Twenty-four males (Big 6) were divided into 3 experimental groups differing in form of Se supplementation (no Se supplementation, 0.3 mg/kg of inorganic Se from sodium selenite and 0.3 mg/kg of organic Se from Sel-Plex, Alltech Inc., Nicholasville, KY). Dietary Se supplementation enhanced the sperm concentration and total number of sperm and did not influence the antioxidative properties of turkey seminal plasma and most biochemical parameters. Only seminal plasma acid phosphatase activity was increased in turkeys fed inorganic Se. The main sperm DNA fragmentation parameters were not affected by dietary Se. The highest percentage of motile spermatozoa (85%) was recorded for the semen of turkeys fed organic Se. Values of the biochemical parameters (acid phosphatase, superoxide dismutase, total antioxidant capacity) of seminal plasma increased during the reproductive season. Yellow semen was characterized by increased biochemical parameters and decreased spermatozoa motility characteristics. However, the percentage of motile spermatozoa did not differ between white and yellow semen. Organic Se seemed to be the preferred form of diet supplementation in comparison with inorganic Se. Biochemical parameters of semen and spermatozoa motility parameters appear to be useful for evaluating the effect of age on semen quality. Monitoring the DNA fragmentation of spermatozoa at the end of the reproductive season could be

  4. Surface Chemistry and Spectroscopy of Chromium in Inorganic Oxides

    NARCIS (Netherlands)

    Weckhuysen, B.M.; Wachs, I.E.; Schoonheydt, R.A.

    1996-01-01

    Focuses on the surface chemistry and spectroscopy of chromium in inorganic oxides. Characterization of the molecular structures of chromium; Mechanics of hydrogenation-dehydrogenation reactions; Mobility and reactivity on oxidic surfaces.

  5. Inorganic Nanostructured High-Temperature Magnet Wires Project

    Data.gov (United States)

    National Aeronautics and Space Administration — This project will develop a high-temperature tolerant electrically-insulating coating for magnet wires. The Phase I program will result in a flexible, inorganic...

  6. Incorporation of inorganic carbon by Antarctic cryptoendolithic fungi

    Science.gov (United States)

    Palmer, R. J. Jr; Friedmann, E. I.

    1988-01-01

    Fungi isolated from the cryptoendolithic community of the Ross Desert are capable of fixing inorganic carbon. Results suggest that lichen mycobionts and parasymbionts are adapted to different water regimes in the cryptoendolithic environment.

  7. Quantification of the release of inorganic elements from biofuels

    DEFF Research Database (Denmark)

    Frandsen, Flemming; van Lith, Simone Cornelia; Korbee, Rob

    2007-01-01

    -scale and pilot-scale fixed-bed release data. In conclusion, it is recommended to perform the described lab-scale tests in order to obtain reliable quantitative data on the release of inorganic elements under grate-firing or suspension-firing conditions. Advanced fuel characterization by use of chemical...... fractionation and simultaneous thermal analysis, and global equilibrium analysis of thermal fuel conversion systems, provide valuable information on the association of inorganic elements in the fuel, the transformations and release of inorganic species upon heating, and the possible forms in which the inorganic...... elements are thermodynamically stable as a function of temperature. This information is needed for the interpretation of the lab-scale release data. Thus, for the purpose of modeling ash or aerosol formation, fuel characterization methods should be combined with lab-scale release measurements. Pilot...

  8. Synthesis, Properties and Mineralogy of Important Inorganic Materials

    DEFF Research Database (Denmark)

    Warner, Terence Edwin

    , ferroelectric, thermoelectric, luminescent, photochromic and magnetic materials; are technologically important classes of material, that are represented by numerous inorganic phases. Yet how many of us are aware of their precise chemical compositions, and have sufficient knowledge to actually make them...

  9. Effects of organic and inorganic amendments on soil erodibility

    Directory of Open Access Journals (Sweden)

    Nutullah Özdemir

    2015-10-01

    Full Text Available The objective of the present investigation is to find out the effect of incorporating of various organic and inorganic matter sources such as lime (L, zeolit (Z, polyacrylamide (PAM and biosolid (BS on the instability index. A bulk surface (0–20 cm depth soil sample was taken from Samsun, in northern part of Turkey. Some soil properties were determined as follows; fine in texture, modarete in organic matter content, low in pH and free of alkaline problem. The soil samples were treated with the inorganic and organic materials at four different levels including the control treatments in a randomized factorial block design. The soil samples were incubated for ten weeks. After the incubation period, corn was grown in all pots. The results can be summarized as organic and inorganic matter treatments increased structure stability and decreased soil erodibility. Effectiveness of the treatments varied depending on the types and levels of organic and inorganic materials.

  10. Modulating semiconductor surface electronic properties by inorganic peptide-binders sequence design.

    Science.gov (United States)

    Matmor, Maayan; Ashkenasy, Nurit

    2012-12-19

    The use of proteins and peptides as part of biosensors and electronic devices has been the focus of intense research in recent years. However, despite the fact that the interface between the bioorganic molecules and the inorganic matter plays a significant role in determining the properties of such devices, information on the electronic properties of such interfaces is sparse. In this work, we demonstrate that the identity and position of single amino acid in short inorganic binding protein-segments can significantly modulate the electronic properties of semiconductor surfaces on which they are bound. Specifically, we show that the introduction of tyrosine or tryptophan, both possessing an aromatic side chain which higher occupied molecular orbitals are positioned in proximity to the edge of GaAs valence band, to the sequence of a peptide that binds to GaAs (100) results in changes of both the electron affinity and surface potential of the semiconductor. These effects were found to be more pronounced than the effects induced by the same amino acids once bound on the surface in a head-tail configuration. Furthermore, the relative magnitude of each effect was found to depend on the position of the modification in the sequence. This sequence dependent behavior is induced both indirectly by changes in the peptide surface coverage, and directly, probably, due to changes in the orientation and proximity of the tyrosine/tryptophan side group with respect to the surface due to the preferred conformation the peptide adopts on the surface. These studies reveal that despite the use of short protein oligomers and aiming at a non-natural-electronic task, the well-known relations between the proteins' structure and function is preserved. Combining the ability to tune the electronic properties at the interface with the ability to direct the growth of inorganic materials makes peptides promising building blocks for the construction of novel hybrid electronic devices and biosensors.

  11. Biomimetic organic-inorganic nanocomposite coatings for titanium implants.

    Science.gov (United States)

    Sikirić, Maja Dutour; Gergely, Csilla; Elkaim, Rene; Wachtel, Ellen; Cuisinier, Frederic J G; Füredi-Milhofer, Helga

    2009-06-01

    A new class of organic-inorganic nanocomposites, to be used as coatings for surface enhancement of metal implants for bone replacement and repair, has been prepared by a biomimetic three-step procedure: (1) embedding amorphous calcium phosphate (ACP) particles between organic polyelectrolyte multilayers (PE MLs), (2) in situ transformation of ACP to octacalcium phospate (OCP) and/or poorly crystalline apatite nanocrystals by immersion of the material into a metastable calcifying solution (MCS) and (3) deposition of a final PE ML. The organic polyelectrolytes used were poly-L-glutamic acid and poly-L-lysine. The nanocomposites obtained by each successive step were characterized by scanning electron microscopy, energy dispersive X-ray analysis (EDS), and XRD, and their suitability as coatings for metal implants was examined by mechanical and in vitro biological tests. Coatings obtained by the first deposition step are mechanically unstable and therefore not suitable. During the second step, upon immersion into MCS, ACP particles were transformed into crystalline calcium phosphate, with large platelike OCP crystals as the top layer. After phase transformation, the nanocomposite was strongly attached to the titanium, but the top layer did not promote cell proliferation. However, when the coating was topped with an additional PE ML (step 3), smoother surfaces were obtained, which facilitated cell adhesion and proliferation as shown by in vitro biological tests using primary human osteoblasts (HO) directly seeded onto the nanocomposites. In fact, cell proliferation on nanocomposites with top PE MLs was far superior than on any of the individual components and was equivalent to proliferation on the golden standard (plastic).

  12. Inorganic-whisker-reinforced polymer composites synthesis, properties and applications

    CERN Document Server

    Sun, Qiuju

    2015-01-01

    Inorganic-Whisker-Reinforced Polymer Composites: Synthesis, Properties and Applications gives a comprehensive presentation of inorganic microcrystalline fibers, or whiskers, a polymer composite filler. It covers whisker synthesis, surface modification, applications for reinforcing polymer-matrix composites, and analysis of resulting filled polymer composites. It focuses on calcium carbonate whiskers as a primary case study, introducing surface treatment methods for calcium carbonate whiskers and factors that influence them.Along with calcium carbonate, the book discusses potassium titanate and

  13. Annual reports in inorganic and general syntheses 1974

    CERN Document Server

    Niedenzu, Kurt

    1975-01-01

    Annual Reports in Inorganic and General Syntheses-1974 presents an organized annual summary of synthetic developments in inorganic chemistry and its related areas. The book discusses the chemistry of simple and complex metal hydrides of main groups I, II, and III, boron, aluminium, gallium, indium, thallium, silicon, germanium, tin, lead, phosphorus, arsenic, antimony, bismuth, chalcogens, halogens, and pseudohalogens. The text also describes the chemistry of scandium, yttrium, lanthanides, actinides, titanium, zirconium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten, ma

  14. Annual reports in inorganic and general syntheses 1972

    CERN Document Server

    Niedenzu, Kurt

    1973-01-01

    Annual Reports in Inorganic and General Syntheses-1972 presents an organized annual summary of synthetic developments in inorganic chemistry and its related areas. The book discusses alkali and alkaline earth elements, alloys, silver, gold, zinc, cadmium, mercury, boron, aluminum, gallium, indium, thallium, yttrium, scandium, lanthanides, actinides, titanium, zirconium, hafnium, Group V and VI transition elements, manganese, technetium, rhenium, iron, cobalt, nickel, ruthenium, osmium, rhodium, and iridium. The text also describes the chemistry of palladium, platinum, silicon, germanium, tin,

  15. Inorganic Chemistry: A Prestigious History and a Bright Future.

    Science.gov (United States)

    Yam, Vivian Wing-Wah

    2015-07-13

    "…︁Inorganic chemistry has evolved from fundamental studies to the forefronts of interdisciplinary research. What was considered to be impossible or elusive has now become feasible. While we still keep our identity as inorganic chemists, the sharp demarcation between the divisions of different subject disciplines or subdisciplines is no longer relevant …︁" Read more in the Editorial by Vivian W.-W. Yam.

  16. Annual reports in inorganic and general syntheses 1973

    CERN Document Server

    Niedenzu, Kurt

    1974-01-01

    Annual Reports in Inorganic and General Syntheses-1973 presents an organized annual summary of synthetic developments in inorganic chemistry and its related areas. The book covers the synthetic aspects and structural or mechanistic features of elements, including the main group hydrides, alkali and alkaline earth elements, boron, aluminium, gallium, indium, thallium, silicon, germanium, tin, and lead, nitrogen, phosphorus, arsenic, antimony, bismuth, chalcogens, halogens and pseudohalogens, and noble gases. The text also discusses the synthetic aspects and structural or mechanistic features of

  17. Holleman-Wiberg's Inorganic Chemistry edited by Nils Wiberg

    Science.gov (United States)

    Jensen, William B.

    2002-08-01

    Despite these reservations, I strongly recommend this book. I found interesting and useful information on every topic I looked up. It is a model of thoroughness and organization and a must reference book for every serious teacher, whether of freshman chemistry or advanced inorganic chemistry. It would also make a wonderful textbook, though its size would naturally limit its use to those schools which offer at least a full year's sequence in inorganic chemistry.

  18. Casting fine grained, fully dense, strong inorganic materials

    Energy Technology Data Exchange (ETDEWEB)

    Brown, Sam W.; Spencer, Larry S.; Phillips, Michael R.

    2015-11-24

    Methods and apparatuses for casting inorganic materials are provided. The inorganic materials include metals, metal alloys, metal hydrides and other materials. Thermal control zones may be established to control the propagation of a freeze front through the casting. Agitation from a mechanical blade or ultrasonic energy may be used to reduce porosity and shrinkage in the casting. After solidification of the casting, the casting apparatus may be used to anneal the cast part.

  19. Near-infrared sensitive organic-inorganic photorefractive device

    Science.gov (United States)

    Marinova, Vera; Liu, Ren-Chung; Lin, Shiuan-Huei; Chen, Ming-Syuan; Lin, Yi-Hsin; Hsu, Ken-Yuh

    2016-10-01

    Organic-inorganic hybrid structure, assembled by Rh-doped Bi12TiO20 crystal and liquid crystal (LC) layer, operating at near-infrared range is proposed and demonstrated. Due to the photorefractive properties of inorganic substrate, light illumination caused a space charge field which acts as a driving force for LC molecules re-alignment and subsequent refractive index modulation. All optically controlled phase retardation ability has been demonstrated supporting possibilities for further infrared applications.

  20. Novel inorganic heterocycles from dimetalated carboranylamidinates.

    Science.gov (United States)

    Harmgarth, Nicole; Gräsing, Daniel; Dröse, Peter; Hrib, Cristian G; Jones, Peter G; Lorenz, Volker; Hilfert, Liane; Busse, Sabine; Edelmann, Frank T

    2014-04-07

    Mono- and dianionic carboranylamidinates are readily available in one-pot reactions directly from o-carborane (1). In situ-monolithiation of 1 followed by treatment with N,N'-diisopropylcarbodiimide, (i)PrN=C=N(i)Pr, or N,N'-dicyclohexylcarbodiimide, CyN=C=NCy, provided the lithium carboranylamidinates (o-C2B10H10C(NH(i)Pr)(=N(i)Pr)-κ(2)C,N)Li(DME) (2a) and (o-C2B10H10C(NH(i)Cy)(=N(i)Cy)-κ(2)C,N)Li(THF)2 (2b). Controlled hydrolysis of 2a,b afforded the free carboranylamidines o-C2B10H11C(NH(i)R)(=N(i)R) (3a: R = (i)Pr, 3b: R = Cy). The first dimetalated carboranylamidinates, o-C2B10H10C(N(i)Pr)(=N(i)Pr)Li2(DME)2 (4a) (DME = 1,2-dimethoxyethane) and o-C2B10H10C(N(i)Pr)(=N(i)Pr)Li2(THF)4 (4b), were prepared in high yield (83% yield) directly from 1 using a simple one-pot synthetic protocol. Treatment of 4b with 2 equiv. of Me3SiCl afforded the disilylated derivative o-C2B10H10-κ(2)C,N-[C(N(i)PrSiMe3)(=N(i)Pr)]SiMe3 (5). Dianionic 4b also served as an excellent precursor for novel inorganic heterocycles incorporating the closo-1,2-C2B10H10 cage, including the unsymmetrical distannene [o-C2B10H10C(N(i)Pr)(=N(i)Pr)-κ(2)C,N]Sn=Sn[((i)PrN)2C(n)Bu]2 (6) and the azaphosphole derivative [o-C2B10H10C(N(i)Pr)(=N(i)Pr)-κ(2)C,N]PPh (7). Surprisingly, it was found that the synthesis of new inorganic ring systems from dianionic carboranylamidinates can also be achieved by employing only 1 equiv. of n-butyllithium in the generation of the anionic carboranylamidinate intermediates. Using this straightforward one-pot synthetic protocol, the Group 14 metallacycles [o-C2B10H10C(NCy)(=NCy)-κ(2)C,N]SiR2 (R = Cl (8), Me (9), Ph (10)) and [o-C2B10H10C(NCy)([=NCy)-κ(2)C,N]GeCl2 (11) have become accessible. The same synthetic strategy could be successfully adapted to prepare the corresponding Group 4 metallocene derivatives Cp2Ti[o-C2B10H10C(NCy)(=NCy)-κ(2)C,N] (12) and Cp2Zr[o-C2B10H10C(NCy)(=NCy)-κ(2)C,N] (13). The molecular structures of 2b, 3b, 4b, 5, 6, 7, 10, 12, and 13 were

  1. High temperature inorganic membranes for separating hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Fain, D.E.; Roettger, G.E. [Oak Ridge K-25 Site, TN (United States)

    1995-08-01

    Effort has continued to accumulate data on the transport of gases over the temperature range from room temperature to 275{degrees}C with inorganic membranes having a range of pore radii from approximately 0.25 nm to 3 mn. An experimental alumina membrane having an estimated mean pore radius of 0.25 nm has been fabricated and tested. Extensive testing of this membrane indicated that the separation factor for helium and carbon tetrafluoride at 250{degrees}C was 59 and the extrapolated high temperature separation factor was 1,193. For safety reasons, earlier flow measurements concentrated on helium, carbon dioxide, and carbon tetrafluoride. New data have been acquired with hydrogen to verify the agreement with the other gases. During the measurements with hydrogen, it was noted that a considerable amount of moisture was present in the test gas. The source of this moisture and its effect on permeance was examined. Improvements were implemented to the flow test system to minimize the water content of the hydrogen test gas, and subsequent flow measurements have shown excellent results with hydrogen. The extrapolation of separation factors as a function of temperature continues to show promise as a means of using the hard sphere model to determine the pore size of membranes. The temperature dependence of helium transport through membranes appears to be considerably greater than other gases for the smallest pore sizes. The effort to extend temperature dependence to the hard sphere model continues to be delayed, primarily because of a lack of adequate adsorption data.

  2. Test Research for Basic Mechanics Performance of Inorganic Polymer Concrete

    Directory of Open Access Journals (Sweden)

    Huihong Liu

    2014-01-01

    Full Text Available The main objective of this study is to evaluate the basic mechanics properties (compressive strength, modulus of elasticity, Poisson’s ratio and splitting tensile strength of inorganic polymer concrete whose mix proportion is ripe recipe and try to provide an experimental and theoretical foundation for application of inorganic polymer concrete in the practical engineering. In this study, the basic mechanics properties of inorganic polymer concrete have been studied by test. At the same time, the same tests researches are made for the common Portland cement concrete for comparison. Through the comparison research, it can be found that the compressive bearing capacity of inorganic polymer concrete is stronger and the modulus of elasticity and Poisson’s ratio is slightly bigger than those of common concrete and that the splitting tensile strength is as poor as those of ordinary Portland cement concrete. In order to investigate its long-term performance, the shrinkage and creep tests of inorganic polymer concrete have been studied as well. The change rules of shrinkage and creep in inorganic polymer concrete with time are obtained. It is that initial deformation is bigger and late deformation gradually becomes small and stable. These rules are basic similar as common Portland cement concrete.

  3. Isolation of living Algae growing in the shells of Molluscs and Barnacles with EDTA (ethylenediaminetetraacetic acid)

    NARCIS (Netherlands)

    Prud’homme van Reine, W.F.; Hoek, van den C.

    1966-01-01

    Several decalcifying mixtures or aqueous solutions of inorganic or organic acids are generally used for releasing algae growing in the shells of molluscs and barnacles, for instance dilute hydrochloric, nitric, citric, or acetic acid (4), a mixture of nitric acid, chromic acid and alcolhol (1), nitr

  4. Modeling the surface tension of complex, reactive organic-inorganic mixtures

    Science.gov (United States)

    Schwier, A. N.; Viglione, G. A.; Li, Z.; McNeill, V. Faye

    2013-11-01

    Atmospheric aerosols can contain thousands of organic compounds which impact aerosol surface tension, affecting aerosol properties such as heterogeneous reactivity, ice nucleation, and cloud droplet formation. We present new experimental data for the surface tension of complex, reactive organic-inorganic aqueous mixtures mimicking tropospheric aerosols. Each solution contained 2-6 organic compounds, including methylglyoxal, glyoxal, formaldehyde, acetaldehyde, oxalic acid, succinic acid, leucine, alanine, glycine, and serine, with and without ammonium sulfate. We test two semi-empirical surface tension models and find that most reactive, complex, aqueous organic mixtures which do not contain salt are well described by a weighted Szyszkowski-Langmuir (S-L) model which was first presented by Henning et al. (2005). Two approaches for modeling the effects of salt were tested: (1) the Tuckermann approach (an extension of the Henning model with an additional explicit salt term), and (2) a new implicit method proposed here which employs experimental surface tension data obtained for each organic species in the presence of salt used with the Henning model. We recommend the use of method (2) for surface tension modeling of aerosol systems because the Henning model (using data obtained from organic-inorganic systems) and Tuckermann approach provide similar modeling results and goodness-of-fit (χ2) values, yet the Henning model is a simpler and more physical approach to modeling the effects of salt, requiring less empirically determined parameters.

  5. Modeling the surface tension of complex, reactive organic-inorganic mixtures

    Directory of Open Access Journals (Sweden)

    A. N. Schwier

    2013-01-01

    Full Text Available Atmospheric aerosols can contain thousands of organic compounds which impact aerosol surface tension, affecting aerosol properties such as cloud condensation nuclei (CCN ability. We present new experimental data for the surface tension of complex, reactive organic-inorganic aqueous mixtures mimicking tropospheric aerosols. Each solution contained 2–6 organic compounds, including methylglyoxal, glyoxal, formaldehyde, acetaldehyde, oxalic acid, succinic acid, leucine, alanine, glycine, and serine, with and without ammonium sulfate. We test two surface tension models and find that most reactive, complex, aqueous organic mixtures which do not contain salt are well-described by a weighted Szyszkowski–Langmuir (S–L model which was first presented by Henning et al. (2005. Two approaches for modeling the effects of salt were tested: (1 the Tuckermann approach (an extension of the Henning model with an additional explicit salt term, and (2 a new implicit method proposed here which employs experimental surface tension data obtained for each organic species in the presence of salt used with the Henning model. We recommend the use of method (2 for surface tension modeling because the Henning model (using data obtained from organic-inorganic systems and Tuckermann approach provide similar modeling fits and goodness of fit (χ2 values, yet the Henning model is a simpler and more physical approach to modeling the effects of salt, requiring less empirically determined parameters.

  6. A new inorganic-organic composite coagulant, consisting of polyferric sulphate (PFS) and polyacrylamide (PAA).

    Science.gov (United States)

    Moussas, P A; Zouboulis, A I

    2009-08-01

    Currently, research is focused on the synthesis of new composite coagulants, which are constituted of both inorganic and organic materials. In this paper, the development of relevant reagents was investigated, by combining the inorganic pre-polymerised iron-based coagulant Polyferric Sulphate (PFS) with an organic, non-ionic polymer (Polyacrylamide, PAA) under different PAA/Fe (mg/l) and OH/Fe molar ratios. Moreover, the new reagents were characterised in terms of typical properties, stability and morphological analysis (XRD, FTIR, SEM). Their coagulation performance, when treating low or high turbid kaolin-humic acid suspensions, was also investigated, whereas the applied coagulation mechanisms were discussed by using the Photometric Dispersion Analysis (PDA) analysis. The results show that the new coagulation reagents present improved properties, including increased effective polymer species concentration, and they exhibit very good stability. The respective tests using PDA confirmed that the predominant coagulation mechanism of PFS-PAA is the bridge formation mechanism. Coagulation experiments in low or high turbid kaolin-humic acid suspensions reveal that the novel composite reagent PFS-PAA exhibits better coagulation performance, when compared with simple PFS, in terms of zeta-potential reduction, turbidity and organic matter removal and residual iron concentration.

  7. Proton Conduction in Sulfonated Organic-Inorganic Hybrid Monoliths with Hierarchical Pore Structure.

    Science.gov (United States)

    von der Lehr, Martin; Seidler, Christopher F; Taffa, Dereje H; Wark, Michael; Smarsly, Bernd M; Marschall, Roland

    2016-09-28

    Porous organic-inorganic hybrid monoliths with hierarchical porosity exhibiting macro- and mesopores are prepared via sol-gel process under variation of the mesopore size. Organic moieties in the pore walls are incorporated by substituting up to 10% of the silicon precursor tetramethylorthosilicate with bisilylated benzene molecules. After functionalization with sulfonic acid groups, the resulting sulfonated hybrid monoliths featuring a bimodal pore structure are investigated regarding proton conduction depending on temperature and relative humidity. The hierarchical pore system and controlled mesopore design turn out to be crucial for sulfonation and proton conduction. These sulfonated hybrid hierarchical monoliths containing only 10% organic precursor exhibit higher proton conduction at different relative humidities than sulfonated periodic mesoporous organosilica made of 100% bisilylated precursors exhibiting solely mesopores, even with a lower concentration of sulfonic acid groups.

  8. Aspartic acid

    Science.gov (United States)

    Aspartic acid is a nonessential amino acids . Amino acids are building blocks of proteins. "Nonessential" means that our ... this amino acid from the food we eat. Aspartic acid is also called asparaginic acid. Aspartic acid helps ...

  9. Rumen Microorganisms Decrease Bioavailability of Inorganic Selenium Supplements.

    Science.gov (United States)

    Galbraith, M L; Vorachek, W R; Estill, C T; Whanger, P D; Bobe, G; Davis, T Z; Hall, J A

    2016-06-01

    Despite the availability of selenium (Se)-enriched trace mineral supplements, we have observed low Se status in cattle and sheep offered traditional inorganic Se supplements. Reasons for this may include inadequate intake or low bioavailability of inorganic Se sources. The objective of this study was to determine whether rumen microorganisms (RMO) alter the bioavailability of Se sources commonly used in Se supplements. Rumen microorganisms were isolated from ewes (n = 4) and incubated ex vivo with no Se (control), with inorganic Na selenite or Na selenate, or with organic selenomethionine (SeMet). Total Se incorporated into RMO and the amount of elemental Se formed were determined under equivalent conditions. Incorporation of Se from Na selenite, Na selenate, or SeMet into RMO was measured as fold change compared with control (no added Se). Incorporation of Se into microbial mass was greater for SeMet (13.2-fold greater than no-Se control) compared with inorganic Se supplements (P = 0.02); no differences were observed between inorganic Na selenate (3.3-fold greater than no-Se control) and Na selenite (3.5-fold greater than no-Se control; P = 0.97). Formation of non-bioavailable, elemental Se was less for RMO incubated with SeMet compared with inorganic Se sources (P = 0.01); no differences were observed between Na selenate and Na selenite (P = 0.09). The clinical importance of these results is that the oral bioavailability of organic SeMet should be greater compared with inorganic Se sources because of greater RMO incorporation of Se and decreased formation of elemental Se by RMO.

  10. APPLICATION OF INFRARED SPECTROSCOPY TO THE ANALYSIS OF INORGANIC NITRATES. PHASE 1. SPECTRA OF INORGANIC NITRATES IN ACETONE AND THE USE OF SUCH SPECTRA IN ANALYTICAL CHEMISTRY

    Science.gov (United States)

    A study was made of the spectra of soluble inorganic nitrates in acetone solution and the use of such spectra in analytical chemistry . The spectra of...solubilities of anhydrous inorganic nitrates in acetone. The applications of the spectra of inorganic nitrates in acetone to analytical chemistry is

  11. Methylation of inorganic mercury in polar marine waters

    Science.gov (United States)

    Lehnherr, Igor; St. Louis, Vincent L.; Hintelmann, Holger; Kirk, Jane L.

    2011-05-01

    Monomethylmercury is a neurotoxin that accumulates in marine organisms, with serious implications for human health. The toxin is of particular concern to northern Inuit peoples, for example, whose traditional diets are composed primarily of marine mammals and fish. The ultimate source of monomethylmercury to marine organisms has remained uncertain, although various potential sources have been proposed, including export from coastal and deep-sea sediments and major river systems, atmospheric deposition and water-column production. Here, we report results from incubation experiments in which we added isotopically labelled inorganic mercury and monomethylmercury to seawater samples collected from a range of sites in the Canadian Arctic Archipelago. Monomethylmercury formed from the methylation of inorganic mercury in all samples. Demethylation of monomethylmercury was also observed in water from all sites. We determined steady-state concentrations of monomethylmercury in marine waters by incorporating the rate constants for monomethylmercury formation and degradation derived from these experiments into a numerical model. We estimate that the conversion of inorganic mercury to monomethylmercury in the water column accounts for around 47% (+/-62%, standard deviation) of the monomethylmercury present in polar marine waters, with site-to-site differences in inorganic mercury and monomethylmercury levels accounting for most of the variability. We suggest that water-column methylation of inorganic mercury is a significant source of monomethylmercury in pelagic marine food webs in the Arctic, and possibly in the world's oceans in general.

  12. Computer-Assisted Inverse Design of Inorganic Electrides

    Science.gov (United States)

    Zhang, Yunwei; Wang, Hui; Wang, Yanchao; Zhang, Lijun; Ma, Yanming

    2017-01-01

    Electrides are intrinsic electron-rich materials enabling applications as excellent electron emitters, superior catalysts, and strong reducing agents. There are a number of organic electrides; however, their instability at room temperature and sensitivity to moisture are bottlenecks for their practical uses. Known inorganic electrides are rare, but they appear to have greater thermal stability at ambient conditions and are thus better characterized for application. Here, we develop a computer-assisted inverse-design method for searching for a large variety of inorganic electrides unbiased by any known electride structures. It uses the intrinsic property of interstitial electron localization of electrides as the global variable function for swarm intelligence structure searches. We construct two rules of thumb on the design of inorganic electrides pointing to electron-rich ionic systems and low electronegativity of the cationic elements involved. By screening 99 such binary compounds through large-scale computer simulations, we identify 24 stable and 65 metastable new inorganic electrides that show distinct three-, two-, and zero-dimensional conductive properties, among which 18 are existing compounds that have not been pointed to as electrides. Our work reveals the rich abundance of inorganic electrides by providing 33 hitherto unexpected structure prototypes of electrides, of which 19 are not in the known structure databases.

  13. Determination of inorganic anions in papermaking waters by ion chromatography

    Directory of Open Access Journals (Sweden)

    DARJA ŽARKOVIĆ

    2009-03-01

    Full Text Available A suppressed ion chromatography (IC method for the determination of inorganic anions in process water from paperboard production was developed and validated. Common inorganic anions (Cl-, NO3-, PO43- and SO42- were detected in fresh and process water samples collected from a paperboard production system at 16 characteristic points. It was shown that the use of an IonPac®-AS14 column under isocratic conditions with Na2CO3/NaHCO3 as the eluent and a suppression device proved to be a reliable analytical solution for the separation of the inorganic anions present in papermaking waters. This IC method is quite satisfactory concerning selectivity and sensitivity, and enables the determination of several inorganic anions over a wide concentration range. According to the obtained results, the total amount of analyzed inorganic anions was below 0.1 g/L, i.e., below the critical value which may trigger operational problems in paper production.

  14. Factor analysis of combined organic and inorganic aerosol mass spectra from high resolution aerosol mass spectrometer measurements

    Directory of Open Access Journals (Sweden)

    Y. L. Sun

    2012-05-01

    Full Text Available The high resolution mass spectra of organic and inorganic aerosols from aerosol mass spectrometer (AMS measurements were first combined into positive matrix factorization (PMF analysis to investigate the sources and evolution processes of atmospheric aerosols. The new approach is able to study the mixing of organic aerosols (OA and inorganic species, the acidity of OA factors, and the fragment ion patterns related to photochemical processing. In this study, PMF analysis of the unified AMS spectral matrices resolved 8 factors for the submicron aerosols measured at Queens College in New York City in summer 2009. The hydrocarbon-like OA (HOA and cooking OA (COA contain very minor inorganic species, indicating the different sources and mixing characteristics between primary OA and secondary species. The two factors that are primarily ammonium sulfate (SO4-OA and ammonium nitrate (NO3-OA, respectively, are overall neutralized, of which the OA in SO4-OA shows the highest oxidation state (O/C = 0.69 among OA factors. The semi-volatile oxygenated OA comprises two components, i.e., a less oxidized (LO-OOA and a more oxidized (MO-OOA. The MO-OOA represents a local photochemical product with the diurnal profile exhibiting a pronounced noon peak, consistent with those of formaldehyde (HCHO and Ox (= O3+NO2. The much higher NO+/NO2+ fragment ion ratio in MO-OOA than that from ammonium nitrate alone provides evidence for the formation of organic nitrates. The amine-related nitrogen-enriched OA (NOA contains ~25% of acidic inorganic salts, elucidating the formation of secondary OA from amines in acidic environments. The size distributions derived from 3-dimensional size-resolved mass spectra show distinct diurnal evolving behaviors for different OA factors, but overall a progressing evolution from smaller to larger particle mode as a function of oxidation states

  15. Low Phytic Acid Barley Responses to Phosphorus Rates

    Science.gov (United States)

    Low phytic acid (LPA) barley (Hordeum vulgare L.) cultivars partition phosphorus in seed tissue differently than conventional barley cultivars through a reduction in seed phytic acid (myo-inositol-1,2,3,4,5,6-hexkisphosphate) coupled with an increase in inorganic phosphorus. The response of the LPA...

  16. Recent progress and applications of ion-exclusion/ion-exchange chromatography for simultaneous determination of inorganic anions and cations.

    Science.gov (United States)

    Nakatani, Nobutake; Kozaki, Daisuke; Mori, Masanobu; Tanaka, Kazuhiko

    2012-01-01

    One of the ultimate goals of ion chromatography is to determine both anions and cations found in samples with a single chromatographic run. In the present article, recent progress in ion-exclusion/ion-exchange chromatography for the simultaneous determinations of inorganic anions and cations are reviewed. Firstly, the principle and the control for the simultaneous separation and detection of analyte ions using ion-exclusion/cation-exchange chromatography with a weakly acidic cation-exchange column are outlined. Then, advanced chromatographic techniques in terms of analytical time, selectively and sensitivity are summarized. As a related method, ion-exclusion/anion-exchange chromatography with an anion-exchange column could be used for the simultaneous determination of inorganic nitrogen species, such as ammonium, nitrite and nitrate ions. Their usefulness and applications to water-quality monitoring and related techniques are also described.

  17. Effects of Long-Term Application of Inorganic Fertilizers on Biochemical Properties of a Rice-Planting Red Soil

    Institute of Scientific and Technical Information of China (English)

    ZHONG Wen-Hui; CAI Zu-Cong; ZHANG He

    2007-01-01

    A long-term experiment was set up in Yingtan of Jiangxi Province to investigate the effects of long-term application of inorganic fertilizers on the biochemical properties of a rice-planting soil derived from Quaternary red earth. Noncultivated soils are extremely eroded and characterized by a low pH and deficiencies in available nutrients, in particular P and N. After 13 years of inorganic fertilization in cultivation for double-cropped rice, the biochemical properties of the soil were changed. The nitrification potential and urease activity were higher in the treatments with N application than those without N application. Acid phosphatase activity and dehydrogenase activity were also higher in the treatments with P application than in those without P application. The dehydrogenase activity correlated well with the concentrations of both total P and hydrolysable N and with rice crop yield, suggesting that dehydrogenase activity might be a suitable indicator for improvement in soil fertility.

  18. Insights into support wettability in tuning catalytic performance in the oxidation of aliphatic alcohols to acids.

    Science.gov (United States)

    Wang, Min; Wang, Feng; Ma, Jiping; Chen, Chen; Shi, Song; Xu, Jie

    2013-07-28

    A superhydrophobic catalyst was prepared by immobilizing Pt nanoparticles on superhydrophobic organic-inorganic hybrid silicas, which showed high activity and selectivity in the oxidation of aliphatic alcohols to carboxylic acids.

  19. The role and fate of inorganic nitrogen species during UVA/TiO₂ disinfection.

    Science.gov (United States)

    Zuo, XiaoJun; Hu, Jiangyong; Chen, MinDong

    2015-09-01

    Inorganic nitrogen species have three states including ammonia nitrogen (NH4(+)/NH3), nitrite (NO2(-)) and nitrate (NO3(-)) and are often found in the disinfection system. However, no available literature could be found on their role and fate in photocatalytic disinfection systems. In this study, batch experiments were conducted to investigate bacteria inactivation, H2O2 generated and inorganic nitrogen variation to understand the role and fate of inorganic nitrogen species during UVA/TiO2 disinfection and evaluate effects of initial pH and bacteria levels on the role and fate. NH4(+)/NH3 and NO2(-) inhibited the photocatalytic disinfection process obviously. It could be confirmed through that H2O2 yield used for pathogen inactivation was dependent on NH4(+)/NH3 and NO2(-) levels. The NH4(+)/NH3 remaining, NH4(+) remaining and NO3(-) yields in only NH4(+)/NH3 photocatalytic oxidation experiments were obviously different from the corresponding values in the photocatalytic disinfection experiments with NH4(+)/NH3, which confirmed that photocatalytic disinfection had an obvious effect on the fate of NH4(+)/NH3. However, photocatalytic disinfection had slight effects on the fate of NO2(-) and NO3(-). Escherischia coli inactivation rate was the highest in neutral solutions (Initial pH 7) while the lowest in alkaline solutions (Initial pH 8.5). The decrease of NH4(+)/NH3 in alkaline solutions was the most significant. In turn, the photocatalysis of NO2(-) was more evident in acidic solutions. E. coli inactivation was reduced with the increase of initial E. coli concentrations. The initial bacteria concentrations significantly influenced the increase of NH4(+)/NH3, NH4(+) and NO3(-), but slightly impacted the decrease of NO2(-).

  20. Apparent Disequilibrium of Inorganic and Organic Carbon Compounds in Serpentinizing Fluids

    Science.gov (United States)

    Robinson, K.; Shock, E.

    2014-12-01

    During serpentinization of ultramafic rocks, ferrous iron in silicates is oxidized to ferric minerals and H2O is reduced to H2. This process is accompanied by the reduction of inorganic carbon, as observed in experiments and natural systems. To test the extent to which stable and metastable equilibria are reached among aqueous organic compounds during serpentinization, we sampled water and dissolved gases from circumneutral surface pools and hyperalkaline seeps in the Samail ophiolite in the Sultanate of Oman and analyzed for various carbon constituents, including dissolved inorganic carbon, dissolved organic carbon, methane, carbon monoxide, formate, acetate, and other small organic acid anions. Measurements of temperature, pH, dissolved H2, O2, major cations, major anions, and major and trace elements were also made. The aqueous composition of the analyzed samples was speciated based on ionic equilibrium interactions in order to obtain activities for inorganic carbon species, reduced carbon species, H2, and O2. The redox disequilibria among carbon species was then assessed using data and parameters for the revised HKF equations of state. This analysis demonstrates that the carbon species in this system are out of equilibrium with respect to one another in ways that cannot be compensated by altering the abundance of the other constituents within analytical uncertainties. Specifically, there is too much formate and too little methane relative to stable and metastable equilibria. This result implies the following: 1) Methane and formate equilibrated in separate parts of the system, given that no reasonable temperature, pressure, or composition changes satisfy equilibrium with their measured abundances. 2) Methane production is kinetically inhibited, as seen in experiments. 3) Microbial methane oxidation altered the abundance of methane and formate; methane oxidation to formate or carbonate is calculated to be extremely thermodynamically favorable in these fluids.

  1. Heterostructures based on inorganic and organic van der Waals systems

    Directory of Open Access Journals (Sweden)

    Gwan-Hyoung Lee

    2014-09-01

    Full Text Available The two-dimensional limit of layered materials has recently been realized through the use of van der Waals (vdW heterostructures composed of weakly interacting layers. In this paper, we describe two different classes of vdW heterostructures: inorganic vdW heterostructures prepared by co-lamination and restacking; and organic-inorganic hetero-epitaxy created by physical vapor deposition of organic molecule crystals on an inorganic vdW substrate. Both types of heterostructures exhibit atomically clean vdW interfaces. Employing such vdW heterostructures, we have demonstrated various novel devices, including graphene/hexagonal boron nitride (hBN and MoS2 heterostructures for memory devices; graphene/MoS2/WSe2/graphene vertical p-n junctions for photovoltaic devices, and organic crystals on hBN with graphene electrodes for high-performance transistors.

  2. Preparation and Characterization of Organic/Inorganic Hybrid Nanofibers

    Institute of Scientific and Technical Information of China (English)

    WU Ning; WEI Qu-fu; LI Qi; XU Wen-zheng

    2006-01-01

    A new class of nanocomposites based on organic and inorganic species integrated at a nanoscale has obtained more attention these years. Organic-inorganic hybrids have both the advantages of organic materials, such as light weight, flexibility and good moldability, and inorganic materials, such as high strength, heat stability and chemical resistance. In this work, PVAc/TiO2 organicinorganic hybrid was prepared by sol-gel process. Electrospinning technique was used to fabricate PVAc/TiO2hybrid nanofibers. The structures and properties of the hybrid nanofibers were characterized by Scanning Electron Microscopy (SEM), Atomic Force Microscope (AFM),Differential Scanning Calorimeter (DSC) and Fouriertransform infrared (FTIR) spectra. SEM and AFM were employed to study the topography of the hybrid nanofibers.The chemical structure of the hybrid nanofibers were examined by FTIR. The DSC scansrevealed the second order transition temperature of the hybrid materials were higher than PVAc.

  3. Organic-inorganic membranes for filtration of corn distillery

    Directory of Open Access Journals (Sweden)

    Myronchuk Valeriy G.

    2016-01-01

    Full Text Available Organic-inorganic membranes were obtained by modification of polymer microfiltration membrane with inorganic ion-exchangers, which form secondary porosity inside macroporous substrate (zirconium hydrophosphate or simultaneously in the macroporous substrate and active layer, depending of the particle size (from ≈50 nm up to several microns. Precipitation of the inorganic constituent is considered from the point of view of Ostwald-Freundlich equation. Such processes as pressing test in deionized water and filtration of corn distillery at 1-6 bar were investigated. Theoretical model allowing to establish fouling mechanism, was applied. It was found that the particles both in the substrate and active layer prevent fouling of the membrane with organics and provide rejection of colloidal particles.

  4. ELABORATION AND CHARACTERIZATION OF HYBRID MATERIALS ORGANIC / INORGANIC

    Directory of Open Access Journals (Sweden)

    O BOUBEKKA

    2010-12-01

    Full Text Available Hybrid materials "organic-inorganic" are the subject of immense interest, allowing both to combine some properties of an inorganic material and a polymer. In this work we have carried out a study on conductive polymers, in general, emphasizing the polyaniline. On the other hand, we have presented the inorganic compounds (NbSe2, and ternary compound Nn3Sn SnNb5Se9. From the chemical method, we had to synthesize the following mixtures: PANI/NbSe2, PANI /, Nn3Sn PANI / SnNb5Se9. The structural study of these new compounds are produced by X-ray diffraction and infrared. The morphology of the resulting mixtures to be studied by scanning electron microscopy.

  5. Chitosan bio-based organic-inorganic hybrid aerogel microspheres.

    Science.gov (United States)

    El Kadib, Abdelkrim; Bousmina, Mosto

    2012-07-02

    Recently, organic-inorganic hybrid materials have attracted tremendous attention thanks to their outstanding properties, their efficiency, versatility and their promising applications in a broad range of areas at the interface of chemistry and biology. This article deals with a new family of surface-reactive organic-inorganic hybrid materials built from chitosan microspheres. The gelation of chitosan (a renewable amino carbohydrate obtained by deacetylation of chitin) by pH inversion affords highly dispersed fibrillar networks shaped as self-standing microspheres. Nanocasting of sol-gel processable monomeric alkoxides inside these natural hydrocolloids and their subsequent CO(2) supercritical drying provide high-surface-area organic-inorganic hybrid materials. Examples including chitosan-SiO(2), chitosan-TiO(2), chitosan-redox-clusters and chitosan-clay-aerogel microspheres are described and discussed on the basis of their textural and structural properties, thermal and chemical stability and their performance in catalysis and adsorption.

  6. One-pot biosynthesis of polymer-inorganic nanocomposites

    Science.gov (United States)

    Geng, Jiaqing; Yang, Dong; Zhu, Yong; Cao, Lichao; Jiang, Zhongyi; Sun, Yan

    2011-06-01

    A biological method is demonstrated to fabricate the polymer-inorganic nanocomposites (PINCs) utilizing bacterium as an efficient and versatile biofactory. Gluconacetobacter xylinum that can produce bacterial cellulose is incubated in the culture medium containing titanium or silica precursor. The PINCs can be acquired under the elaborate control of the culturing condition of G. xylinum, in which the formation of inorganic nanoparticles about several tens of nanometers in size synchronizes the fabrication of reticulated bacterial cellulose membrane composed of dense and finely branched nanofibers about 60-120 nm in diameter. The composition and chemical states, morphology, thermal stability of the inorganic nanoparticles, and nanocomposites were extensively characterized. A tentative mechanism for the formation of PINCs is proposed. It is hoped that this study may establish a generic platform toward facile and green synthesis of nanocomposite materials.

  7. One-pot biosynthesis of polymer-inorganic nanocomposites

    Energy Technology Data Exchange (ETDEWEB)

    Geng Jiaqing [Tianjin University, Key Laboratory for Green Technology, School of Chemical Engineering and Technology (China); Yang Dong [Tianjin University, Department of Biochemical Engineering and Key Laboratory of Systems Bioengineering of Ministry of Education, School of Chemical Engineering and Technology (China); Zhu Yong; Cao Lichao; Jiang Zhongyi, E-mail: zhyjiang@tju.edu.cn [Tianjin University, Key Laboratory for Green Technology, School of Chemical Engineering and Technology (China); Sun Yan [Tianjin University, Department of Biochemical Engineering and Key Laboratory of Systems Bioengineering of Ministry of Education, School of Chemical Engineering and Technology (China)

    2011-06-15

    A biological method is demonstrated to fabricate the polymer-inorganic nanocomposites (PINCs) utilizing bacterium as an efficient and versatile biofactory. Gluconacetobacter xylinum that can produce bacterial cellulose is incubated in the culture medium containing titanium or silica precursor. The PINCs can be acquired under the elaborate control of the culturing condition of G. xylinum, in which the formation of inorganic nanoparticles about several tens of nanometers in size synchronizes the fabrication of reticulated bacterial cellulose membrane composed of dense and finely branched nanofibers about 60-120 nm in diameter. The composition and chemical states, morphology, thermal stability of the inorganic nanoparticles, and nanocomposites were extensively characterized. A tentative mechanism for the formation of PINCs is proposed. It is hoped that this study may establish a generic platform toward facile and green synthesis of nanocomposite materials.

  8. Controlling the fate of roxarsone and inorganic arsenic in poultry litter.

    Science.gov (United States)

    Makris, Konstantinos C; Salazar, Jason; Quazi, Shahida; Andra, Syam S; Sarkar, Dibyendu; Bach, Stephan B H; Datta, Rupali

    2008-01-01

    A growing body of literature reports 3-nitro-4-hydroxyphenylarsonic acid (roxarsone) degradation in poultry litter (PL) to the more toxic inorganic arsenic (As). Aluminum-based drinking-water treatment residuals (WTR) present a low-cost amendment technology to reduce As availability in PL, similar to the use of alum to reduce phosphorus availability. Batch experiments investigated the effectiveness of WTR in removing roxarsone and inorganic As species from PL aqueous suspensions. Incubation experiments with WTR-amended PL evaluated the effects of WTR application rates (2.5-15% by weight) and incubation time (up to 32 d) at two incubation temperatures (23 and 35 degrees C) on As availability in PL. Batch PL aqueous experiments showed the high affinity of As(V), As(III), dimethylarsinic acid (DMA), monomethylarsonic acid (MMA), and roxarsone for the WTR. The 10% WTR amendment rate decreased As availability in PL by half of that of the unamended (no WTR) PL-incubated samples. The reduction in dissolved As concentrations during incubation of WTR-amended PL samples was kinetically limited, being complete within 13 d. Parallel reductions in roxarsone, As(V), and DMA concentrations were observed with liquid chromatography-inductively coupled plasma mass spectrometry, whereas As(III) and MMA concentrations were always 0.05) influence dissolved As concentrations in the WTR-amended PL. Potential formation of a copper-containing roxarsone metabolite was considered in PL aqueous suspensions with the aid of electrospray mass spectrometry. Further experiments in the field are necessary to ensure that sorbed As is stable in WTR-amended PL.

  9. Distribution of inorganic and organic substances in the hydrocyclone separated Slovak sub-bituminous coal

    Energy Technology Data Exchange (ETDEWEB)

    Anton Zubrik; Slavomir Hredzak; Ludmila Turcaniova; Michal Lovas; Ingo Bergmann; Klaus Dieter Becker; Maria Lukcova; Vladimir Sepelak [Slovak Academy of Sciences, Kosice (Slovakia). Institute of Geotechnics

    2010-08-15

    A low-rank Slovak sub-bituminous coal from the Handlova deposit was physically treated by washing in a water-only cyclone with the goal to find the separation effect for inorganic (mainly Fe-bearing minerals) and organic substances (humic acids, diterpanes). A high-quality coal product with the ash content in the dry matter of 9.02% and carbon content of C{sup d} = 68.12% at a mass yield of 29.51% was obtained using the water-only cyclone processing. At first, the physically treated coal samples were detailed characterized by XRD, {sup 57}Fe Moessbauer spectroscopy, FT-IR and HR-TEM. In addition to non-crystalline organic coal components, inorganic compounds belonging to silicate minerals (kaolinite, muscovite and quartz) as well as to Fe-bearing sulphide minerals (pyrite) were identified in the sub-bituminous coal by XRD. {sup 57}Fe Moessbauer spectroscopy detected the presence of iron carbonate (siderite), iron-containing clay mineral and two sulphur-containing minerals (pyrite, jarosite) in the untreated coal. On the other hand, only one Fe-bearing mineral, (pyrite) was found in the washed coal. Effect of the physical separation is also demonstrated in FT-IR spectra, where the peak at 1040 cm{sup -1} representing the silicate component in the untreated sample is not detectable in the washed coal sample. Presence of extractive organic substances, i.e. humic acids and tetracyclic diterpane (16a(H)-phyllocladane), in the hydrocyclone products is also evidenced. It was confirmed that the isolated diterpenoic compound is attendant in the washed product with the lowest ash content and it is assimilated with the organic part of coal. Surprisingly, humic acids were found in the highest concentration in the slurry that has the highest content of ash (63.14%). 54 refs., 8 figs., 5 tabs.

  10. Modeling the Detection of Organic and Inorganic Compounds Using Iodide-Based Chemical Ionization.

    Science.gov (United States)

    Iyer, Siddharth; Lopez-Hilfiker, Felipe; Lee, Ben H; Thornton, Joel A; Kurtén, Theo

    2016-02-04

    Iodide-based chemical ionization mass spectrometry (CIMS) has been used to detect and measure concentrations of several atmospherically relevant organic and inorganic compounds. The significant electronegativity of iodide and the strong acidity of hydroiodic acid makes electron transfer and proton abstraction essentially negligible, and the soft nature of the adduct formation ionization technique reduces the chances of sample fragmentation. In addition, iodide has a large negative mass defect, which, when combined with the high resolving power of a high resolution time-of-flight chemical ionization mass spectrometer (HR-ToF-CIMS), provides good selectivity. In this work, we use quantum chemical methods to calculate the binding energies, enthalpies and free energies for clusters of an iodide ion with a number of atmospherically relevant organic and inorganic compounds. Systematic configurational sampling of the free molecules and clusters was carried out at the B3LYP/6-31G* level, followed by subsequent calculations at the PBE/SDD and DLPNO-CCSD(T)/def2-QZVPP//PBE/aug-cc-pVTZ-PP levels. The binding energies, enthalpies, and free energies thus obtained were then compared to the iodide-based University of Washington HR-ToF-CIMS (UW-CIMS) instrument sensitivities for these molecules. We observed a reasonably linear relationship between the cluster binding enthalpies and logarithmic instrument sensitivities already at the PBE/SDD level, which indicates that relatively simple quantum chemical methods can predict the sensitivity of an iodide-based CIMS instrument toward most molecules. However, higher level calculations were needed to treat some outlier molecules, most notably oxalic acid and methylerythritol. Our calculations also corroborated the recent experimental findings that the molecules that the UW-CIMS detects at maximum sensitivity usually have binding enthalpies to iodide which are higher than about 26 kcal/mol, depending slightly on the level of theory.

  11. Exposure to inorganic arsenic in soil increases urinary inorganic arsenic concentrations of residents living in old mining areas.

    Science.gov (United States)

    Hinwood, Andrea L; Sim, Malcolm R; Jolley, Damien; de Klerk, Nick; Bastone, Elisa B; Gerostamoulos, Jim; Drummer, Olaf H

    2004-03-01

    The short term human exposure studies conducted on populations exposed to high concentrations of inorganic arsenic in soil have been inconsistent in demonstrating a relationship between environmental concentrations and exposure measures. In Australia there are many areas with very high arsenic concentrations in residential soil most typically associated with gold mining activities in rural areas. This study aimed to investigate the relationship between environmental arsenic and urinary inorganic arsenic concentrations in a population living in a gold mining area (soil arsenic concentrations between 9 and 9900 mg kg(-1)), and a control population with low arsenic levels in soil (between 1 and 80 mg kg(-1)). Risk factors for increased urinary arsenic concentrations were also explored. There was a weak but significant relationship between soil arsenic concentrations and inorganic urinary arsenic concentration with a Spearman correlation coefficient of 0.39. When participants with greater than 100 mg kg(-1) arsenic in residential soil were selected, the coefficient increased to 0.64. The geometric mean urinary inorganic arsenic concentration for the exposed group was 1.64 microg L(-1) (risk factors. These results show that high concentrations of arsenic in soil can make a contribution to urinary inorganic arsenic concentrations.

  12. A Lewis acid catalytic core sandwiched by inorganic polyoxoanion caps: selective H2O2-based oxidations with [Al(III)4(H2O)10(β-XW9O33H)2](6-) (X = As(III), Sb(III)).

    Science.gov (United States)

    Carraro, Mauro; Bassil, Bassem S; Sorarù, Antonio; Berardi, Serena; Suchopar, Andreas; Kortz, Ulrich; Bonchio, Marcella

    2013-09-18

    The Al(III)-containing polyanions [Al(III)4(H2O)10(β-XW9O33H)2](4-) with X = As(III) (1) and Sb(III) (2) feature four aluminum(III) centers sandwiched by two trivacant (β-XW9O33) Keggin units, and trigger peroxide catalysis as well as substrate coordination via multiple Lewis acid site interactions.

  13. A positively charged silver nanowire membrane for rapid on-site swabbing extraction and detection of trace inorganic explosives using a portable Raman spectrometer

    Institute of Scientific and Technical Information of China (English)

    Yu-e Shi; Wenshou Wang; Jinhua Zhan

    2016-01-01

    The sensitive and on-site detection of inorganic explosives has raised serious concerns regarding public safety.However,high stability and non-volatility features currently limit their rapid on-site detection.Surface-enhanced Raman spectroscopy (SERS) is emerging as a powerful technique for the trace-level detection of different molecules.Plasmonic Ag nanowires were produced by a hydrothermal synthesis method using polyvinylpyrrolidone (PVP) as a negatively charged stabilizer.Here,we report a rapid detection method for inorganic explosives based on a simple surface swab with a positively charged diethyldithiocarbamate-modified Ag nanowire membrane coupled with SERS.This membrane,serving as an excellent SERS substrate with high uniformity,stability,and reusability,can capture both typical oxidizers in inorganic explosives and organic nitro-explosives,via electrostatic interaction.The detection level of perchlorates (ClO4-),chlorates (ClO3-),nitrates (NO3-),picric acid,and 2,4-dinitrophenol is as high as 2.0,1.7,0.1,45.8,and 36.6 ng,respectively.In addition,simulated typical inorganic explosives such as black powders,firecrackers,and match heads could also be detected.We believe that this membrane represents an attractive alternative for rapid on-site detection of inorganic explosives with high efficiency.

  14. Inorganic electret with enhanced charge stability for energy harvesting

    DEFF Research Database (Denmark)

    Wang, Fei; Hansen, Ole

    2013-01-01

    We report a new surface treatment of inorganic electret materials which enhances the charge stability. Coating the surfaces with 1H, 1H, 2H, 2H - perfluorodecyltrichlorosilane (FDTS) makes the electret surface more hydrophobic which improves the surface charge stability under high humidity condit...... conditions. Thermal tests show that the thermal stability of charge in the inorganic electrets is also much better than that of polymer materials such as CYTOP. A demonstrator device with SiO2 electrets shows promising results for energy harvesting applications....

  15. Organic and inorganic osmolytes at lipid membrane interfaces

    DEFF Research Database (Denmark)

    Westh, P.; Peters, Günther H.j.

    2008-01-01

    and inorganic components. Before turning to the physicochemical discussion of interfacial interactions, the chapter outlines some central parts of the biology and biotechnology of organic osmolytes. It reviews the central relationships in preferential interaction theory, which we use in subsequent paragraphs......This chapter discusses the interactions of organic osmolytes and membranous interfaces, and the effects of these interactions on the properties of the membrane. It also includes a treatment of inorganic ions at the membrane interface since osmolyte effects involve a balance between organic...

  16. Hybrid Organic/Inorganic Nanocomposites for Photovoltaic Cells

    Directory of Open Access Journals (Sweden)

    Ruchuan Liu

    2014-04-01

    Full Text Available Inorganic/organic hybrid solar cells have attracted a lot of interest due to their potential in combining the advantages of both components. To understand the key issues in association with photoinduced charge separation/transportation processes and to improve overall power conversion efficiency, various combinations with nanostructures of hybrid systems have been investigated. Here, we briefly review the structures of hybrid nanocomposites studied so far, and attempt to associate the power conversion efficiency with these nanostructures. Subsequently, we are then able to summarize the factors for optimizing the performance of inorganic/organic hybrid solar cells.

  17. Development of Inorganic Solar Cells by Nano-technology

    Institute of Scientific and Technical Information of China (English)

    Yafei Zhang; HueyLiang Hwang; Huijuan Geng; Zhihua Zhou; Jiang Wu; Zhiming Wang; Yaozhong Zhang; Zhongli Li; Liying Zhang; Zhi Yang

    2012-01-01

    Inorganic solar cells, as durable photovoltaic devices for harvesting electric energy from sun light, have received tremendous attention due to the fear of exhausting the earth’s energy resources and damaging the living environment due to greenhouse gases. Some recent developments in nanotechnology have opened up new avenues for more relevant inorganic solar cells produced by new photovoltaic conversion concepts and effective solar energy harvesting nanostructures. In this review, the multiple exciton generation effect solar cells, hot carrier solar cells, one dimensional material constructed asymmetrical schottky barrier arrays, noble nanoparticle induced plasmonic enhancement, and light trapping nanostructured semiconductor solar cells are highlighted.

  18. Inorganic Materials Database for Exploring the Nature of Material

    Science.gov (United States)

    Xu, Yibin; Yamazaki, Masayoshi; Villars, Pierre

    2011-11-01

    An inorganic materials database system, AtomWork, has been developed and released on the Internet. It includes the phase diagram, crystal structure, X-ray powder diffraction, and property data of more than 80,000 inorganic materials extracted from scientific literature. The feature of this database is that the information of the synthesis, identification, and property of materials is organically linked, which enables the data reported in different papers to be grouped and compared at four different levels: chemical system, compound, substance, and material. The database can provide users with a comprehensive overview of substances and necessary information to understand the relationships among chemical component, structure, and property.

  19. Corrosion inhibition of a hygroscopic inorganic dust-depressor

    Institute of Scientific and Technical Information of China (English)

    Longzhe Jin; Lu Wang; Dongke Chen

    2006-01-01

    Metallic corrosion is a serious problem in the application of a hygroscopic inorganic dust-depressor. The basic characteristics of a hygroscopic inorganic dust-depressor and its corrosivity, corrosion mechanism, as well as the principle of corrosion inhibition were analyzed. The static mass-loss test was carried out to investigate the corrosion behavior and the effect of the dustdepressor. The static corrosion rates of steel specimens were measured in six different corrosion inhibitor solutions of the dustdepressor, and the suitable corrosion inhibitors for the dust-depressor to reduce the corrosivity were found out.

  20. Supramolecular organization in organic-inorganic heterogeneous hybrid catalysts formed from polyoxometalate and poly(ampholyte) polymer.

    Science.gov (United States)

    Raj, Gijo; Swalus, Colas; Guillet, Alain; Devillers, Michel; Nysten, Bernard; Gaigneaux, Eric M

    2013-04-01

    Hybridization of polyoxometalates (POMs) via the formation of an organic-inorganic association constitutes a new route to develop a heterogeneous POM catalyst with tunable functionality imparted through supramolecular assembly. Herein, we report on strategies to obtain tunable well-defined supramolecular architectures of an organic-inorganic heterogeneous hybrid catalyst formed by the association of a hydrophobically substituted polyampholyte copolymer (poly N, N-diallyl-N-hexylamine-alt-maleic acid) and phosphotungstic acid (H3PW12O40) POMs. The self-assembling property of the initial polyampholyte copolymer matrix is modulated by controlling the pH of the hybridization solution. When deposited on a mica surface, isolated, long and extended polymer chains are formed under basic conditions (pH 7.9), while globular or coiled structures are formed under acidic conditions (pH 2). The supramolecular assembly of the POM-polymer hybrid is found to be directed by the type and quantities of charges present on the polyampholyte copolymer, which themselves depend on the pH conditions. The hypothesis is that the Keggin type [PW12O40](3-) anions, which have a size of ~1 nm, electrostatically bind to the positive charge sites of the polymer backbone. The hybrid material stabilized at pH 5.3 consists of POM-decorated polymer chains. Statistical analysis of distances between pairs of POM entities show narrow density distributions, suggesting that POM entities are attached to the polymer chains with a high level of order. Conversely, under acidic conditions (pH 2), the hybrid shows the formation of a core-shell type of structure. The strategies reported here, to tune the supramolecular assembly of organic-inorganic hybrid materials, are highly valuable for the design and a more rational utilization of POM heterogeneous catalysts in several chemical transformations.

  1. Chemical Species of Aluminum Lons in Acid Soils

    Institute of Scientific and Technical Information of China (English)

    XURENKOU; JIGUOLIANG

    1998-01-01

    Soil samples collected from several acid soils in Guangdong,Fujian,Zhejiang and Anhui provinces of the southern China were employded to characterize the chemical species of aluminum ions in the soils.The proportion or monoeric inorganic Al to total Al in soil solution was in the range of 19% to 70%,that of monomeric organlic Al (Al-OM) to total Al ranged from 7.7% to 69%,and that of the acid-soluble Al to total Al was generally smaller and was lower than 20% in most of the acid soils studied ,The Al-OM concentration in soil solution was postively correlated with the content of dissolved organic carbon(DOC) and aslo affected by the concentration of Al3+,The complexes of aluminum with fluoride(Al-F) were the predominant forms of inorganic Al,and the proportion of Al-F compexes to total inorganic Al increased with pH.Under strongly acid ondition,Al3+ was also a mjaor form of inorganic Al,and the proportio of Al3+ to total inorganic Al decreased with increasing pH.The,proportions of Al-OH and Al-SO4 complexes to total inorganic Al were small and were not larger than 10% in the most acid soils.The concentration of inorganic Al in solution depended largely on pH and the concentration of total F in soil solution,The concentrations of Al-OM,Al3+,Al-F and Al-OH complexes in topsoil were higher than those in subsoil and decreased with the increase in soil depth,The chemical species of aluminum ions were influenced by pH,The concentrations of Al-OM, Al3+,Al-F complexes and Al-OH complexes decreased with the increase in pH.

  2. Determination of inorganic contaminants in water

    Energy Technology Data Exchange (ETDEWEB)

    Cidu, R. [Cagliari Univ. (Italy). Dipt. di Scienze della Terra

    1998-12-31

    The determination of trace elements in water requires to follow adequate sampling and stabilization procedures. Filtration is carried out in situ using a metal-free system under oxygen-free conditions. Addition of acid for a ph value<1 prevents metal precipitation and/or adsorption onto the container walls. Field blank solutions prepared with the same procedure as with samples are necessary to monitor potential contamination. Ultrapure reagents are required to minimize contamination and to achieve the lowest detection limit. Significant improvements in detection limits can be obtained using a preconcentration method (e.g. evaporation, ion exchange, metal extraction into organic solvent). Analytical errors can be estimated using different techniques and analysing certified reference solutions. The determination of major components prior to trace element analysis allows samples to be sorted on increasing salinity contributing to reduce memory effects between samples, dilution can be used to reduce matrix effects, and the use of internal standards is efficient for instrumental drift correction.

  3. Electrochromic conductive polymer fuses for hybrid organic/inorganic semiconductor memories

    Science.gov (United States)

    Möller, Sven; Forrest, Stephen R.; Perlov, Craig; Jackson, Warren; Taussig, Carl

    2003-12-01

    We demonstrate a nonvolatile, write-once-read-many-times (WORM) memory device employing a hybrid organic/inorganic semiconductor architecture consisting of thin film p-i-n silicon diode on a stainless steel substrate integrated in series with a conductive polymer fuse. The nonlinearity of the silicon diodes enables a passive matrix memory architecture, while the conductive polyethylenedioxythiophene:polystyrene sulfonic acid polymer serves as a reliable switch with fuse-like behavior for data storage. The polymer can be switched at ˜2 μs, resulting in a permanent decrease of conductivity of the memory pixel by up to a factor of 103. The switching mechanism is primarily due to a current and thermally dependent redox reaction in the polymer, limited by the double injection of both holes and electrons. The switched device performance does not degrade after many thousand read cycles in ambient at room temperature. Our results suggest that low cost, organic/inorganic WORM memories are feasible for light weight, high density, robust, and fast archival storage applications.

  4. Preliminary Tests Concerning Zero-Valent Iron Efficiency in Inorganic Pollutants Remediation

    Directory of Open Access Journals (Sweden)

    Silvia Fiore

    2009-01-01

    Full Text Available Problem statement: This study was aimed to a preliminary evaluation of the applicability of granular Zero-Valent Iron (ZVI to the on site remediation of groundwater polluted by inorganic contaminants by means of a Permeable Reactive Barrier (PRB. A particular interest was devoted to groundwater impacted by Acid Mine Drainage (AMD that was caused by the oxidation of metal sulphide minerals contained in mine wastes, especially iron disulphide pyrite. Although AMD consequences were particularly evident in surface waters, the percolation through mine wastes may heavily alter the groundwater quality, therefore is particularly important the development of a restrained cost remediation technique for groundwater polluted by AMDs. Approach: In this study the degradation efficiency of Brown size 8/50 ZVI (Peerless Powders and Abrasive Inc., Detroit, US was evaluated performing a leaching column test and analyzing the Oxidation Reduction Potential (ORP, metals, nitrates, chlorides and sulphates profiles along the column. Results: This test allowed simulating the solid-liquid contact characteristic of a real PRB behavior that proved to be a possible solution for the remediation of inorganic pollutants in groundwater. Conclusion: The considered material showed efficiency above 99% in metals removal, although further tests, involving biotic processes and more reducing conditions, are necessary to improve the degradation of sulphates and nitrates.

  5. The formation of organic (propolis films)/inorganic (layered crystals) interfaces for optoelectronic applications

    Science.gov (United States)

    Drapak, S. I.; Bakhtinov, A. P.; Gavrylyuk, S. V.; Kovalyuk, Z. D.; Lytvyn, O. S.

    2008-10-01

    Propolis (honeybee glue) organic films were prepared from an alcoholic solution on the surfaces of inorganic layered semiconductors (indium, gallium and bismuth selenides). Atomic force microscopy (AFM) and X-ray diffraction (XRD) are used to characterize structural properties of an organic/inorganic interfaces. It is shown that nanodimensional linear defects and nanodimensional cavities of various shapes are formed on the van der Waals (VDW) surfaces of layered crystals as a result of chemical interaction between the components of propolis (flavonoids, aminoacids and phenolic acids) and the VDW surfaces as well as deformation interaction between the VDW surfaces and propolis films during their polymerization. The nanocavities are formed as a result of the rupture of strong covalent bonds in the upper layers of layered crystals and have the shape of hexagons or triangles in the (0001) plane. The shape, lateral size and distribution of nanodimensional defects on the VDW surfaces depends on the type of crystals, the magnitude and distribution of surface stresses. We have obtained self-organized nanofold structures of propolis/InSe interface. It is established that such heterostructures have photosensitivity in the infrared range hν<1.2 eV (the values of energy gap are 1.2 eV for InSe and 3.07 eV for propolis films at room temperature).

  6. Synthesis of organic-inorganic hybrid microspheres and the corresponding mesoporous silica nanoparticles.

    Science.gov (United States)

    Liu, Bin; Fu, Xiaomeng; Wang, Dan; Zhang, Wei; Yang, Xinlin

    2013-12-01

    Poly(methacrylic acid-co-3-(methacryloxy)propyltrimethoxysilane) (P(MAA-co-MPS)) organic-inorganic hybrid microspheres were prepared by distillation-precipitation copolymerization of MAA and MPS in acetonitrile in absence of any surfactant and additive. The resultant hybrids had a spherical shape when the MPS inorganic precursor was varied from 0% to 60% in the comonomers during the polymerization. The hybrid microspheres can be facilely cross-linked via the hydrolysis of methoxy groups of polyMPS network and further self-condensation of the hydroxyl groups of silanols. As a result, the hybrid microspheres were facilely converted to mesoporous silica particles via the removal of the organic component through calcination. The narrow dispersed mesoporous silica had a high surface area of 554.2 m(2)/g as well as the average pore size of 8 nm and pore volume of 0.24 cm(3)/g. The corresponding microspheres were characterized by TEM, FT-IR, TGA, and nitrogen sorption-desorption.

  7. Electricity generation from an inorganic sulfur compound containing mining wastewater by acidophilic microorganisms.

    Science.gov (United States)

    Ni, Gaofeng; Christel, Stephan; Roman, Pawel; Wong, Zhen Lim; Bijmans, Martijn F M; Dopson, Mark

    2016-09-01

    Sulfide mineral processing often produces large quantities of wastewaters containing acid-generating inorganic sulfur compounds. If released untreated, these wastewaters can cause catastrophic environmental damage. In this study, microbial fuel cells were inoculated with acidophilic microorganisms to investigate whether inorganic sulfur compound oxidation can generate an electrical current. Cyclic voltammetry suggested that acidophilic microorganisms mediated electron transfer to the anode, and that electricity generation was catalyzed by microorganisms. A cation exchange membrane microbial fuel cell, fed with artificial wastewater containing tetrathionate as electron donor, reached a maximum whole cell voltage of 72 ± 9 mV. Stepwise replacement of the artificial anolyte with real mining process wastewater had no adverse effect on bioelectrochemical performance and generated a maximum voltage of 105 ± 42 mV. 16S rRNA gene sequencing of the microbial consortia resulted in sequences that aligned within the genera Thermoplasma, Ferroplasma, Leptospirillum, Sulfobacillus and Acidithiobacillus. This study opens up possibilities to bioremediate mining wastewater using microbial fuel cell technology.

  8. Controlled Microstructure and Photochromism of Inorganic-organic Thin Films by Ultrasound

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A series of inorganic-organic thin films based on uniformly dispersed nanoparticles of polyoxometalates (POM)entrapped in polyacrylamide (PAM) matrix were prepared by ultrasonic method with different irradiation time.The microstructure, photochromic behavior and mechanism of the films were studied by transmission electron microscopy (TEM), ultraviolet-visible spectra (UV-VIS) and Fourier transform-infrared spectroscopy (FT-IR).The microstructure and photochromic properties of the hybrid thin films could be controlled by ultrasound.TEM image revealed that the average size of phosphotungstic acid (PWA) nanoparticles decreased from 20 to 10 nm with the ultrasound irradiation time from 30 to 60 min. After irradiated with ultraviolet light,the transparent films changed from colorless to blue and showed reversible photochromism. The hybrid film, with ultrasound irradiation for 60 min had higher photochromic efficiency and faster bleaching reaction than the one with ultrasound irradiation for 30 min. FT-IR spectra showed that the Keggin geometry of heteropolyoxometalate was still preserved inside the composites, and the interactions between polyanions and polymer matrix increased as the ultrasound time prolonged. It is suggested that the mechanism of the different photochromic properties for the inorganic-organic thin films is the variation of the microstructure and interfacial interactions induced by ultrasound.

  9. Fabrication and Characterisation of Polyaniline/Laponite based Semiconducting Organic/Inorganic Hybrid Material

    Directory of Open Access Journals (Sweden)

    Walt V.K. Wheelwright

    2014-05-01

    Full Text Available Novel organic-inorganic semiconducting hybrid material is developed by chemically grafting polyaniline (PANI onto an inorganic template, Laponite. The surface active silanol groups of the Laponite sheets were silylated with an aniline functionalised 3-phenylaminopropyltrimethoxysilane (PAPTMOS coupling agent followed by deposition of PANI onto the silylated surface. The method includes the reaction of Laponite with PAPTMOS dissolved in a very small amount of methanol at 110 °C for 44 h in a vacuum oven, interaction of the silylated product with PANI via in situ polymerisation of aniline and one-step isolation process by means of the removal of the non-connected PANI with N-methylpyrrolidinone-diethylamine binary solvent. After isolation and re-doping with methane sulfonic acid the Laponite-PAPTMOS-PANI hybrid becomes electrically conductive. The chemical attachment of PANI with silylated Laponite in the hybrids were characterised by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, elemental analysis, and scanning electron microscopy.Defence Science Journal, Vol. 64, No. 3, May 2014, pp. 193-197, DOI:http://dx.doi.org/10.14429/dsj.64.7185

  10. Method and importance of obtaining humic and fulvic acids of high purity

    Science.gov (United States)

    Malcolm, R.L.

    1976-01-01

    A detailed procedure incorporating centrifugation, pressure filtration, dialysis, resin exchange, and freeze drying is given for the extraction and purification of fulvic and humic acids from soils and sediments. By use of the procedure humic acids have been prepared which have less than 0.22 percent ash. The isolation of relatively ash-free natural organic matter preparations is an essential prerequisite to the characterization of organic reactivity in natural systems. Inorganic impurities of amorphous and crystalline clay minerals and various inorganic metal ions often lead to numerous complications and errors during experimentation with organic matter because the inorganic substances associated with the organic phase cause variable reactivity of the organic substances.

  11. Inorganic pyrophosphatase in uncultivable hemotrophic mycoplasmas: identification and properties of the enzyme from Mycoplasma suis

    Directory of Open Access Journals (Sweden)

    Wittenbrink Max M

    2010-07-01

    Full Text Available Abstract Background Mycoplasma suis belongs to a group of highly specialized hemotrophic bacteria that attach to the surface of host erythrocytes. Hemotrophic mycoplasmas are uncultivable and the genomes are not sequenced so far. Therefore, there is a need for the clarification of essential metabolic pathways which could be crucial barriers for the establishment of an in vitro cultivation system for these veterinary significant bacteria. Inorganic pyrophosphatases (PPase are important enzymes that catalyze the hydrolysis of inorganic pyrophosphate PPi to inorganic phosphate Pi. PPases are essential and ubiquitous metal-dependent enzymes providing a thermodynamic pull for many biosynthetic reactions. Here, we describe the identification, recombinant production and characterization of the soluble (sPPase of Mycoplasma suis. Results Screening of genomic M. suis libraries was used to identify a gene encoding the M. suis inorganic pyrophosphatase (sPPase. The M. suis sPPase consists of 164 amino acids with a molecular mass of 20 kDa. The highest identity of 63.7% was found to the M. penetrans sPPase. The typical 13 active site residues as well as the cation binding signature could be also identified in the M. suis sPPase. The activity of the M. suis enzyme was strongly dependent on Mg2+ and significantly lower in the presence of Mn2+ and Zn2+. Addition of Ca2+ and EDTA inhibited the M. suis sPPase activity. These characteristics confirmed the affiliation of the M. suis PPase to family I soluble PPases. The highest activity was determined at pH 9.0. In M. suis the sPPase builds tetramers of 80 kDa which were detected by convalescent sera from experimentally M. suis infected pigs. Conclusion The identification and characterization of the sPPase of M. suis is an additional step towards the clarification of the metabolism of hemotrophic mycoplasmas and, thus, important for the establishment of an in vitro cultivation system. As an antigenic and conserved

  12. Review of inorganic nitrogen transformations and effect of global climate change on inorganic nitrogen cycling in ocean ecosystems

    Science.gov (United States)

    Kim, Haryun

    2016-03-01

    Inorganic N transformations (nitrification, anaerobic ammonium oxidation, denitrification, and dissimilatory nitrate reduction to ammonium) are regulated by various biogeochemical factors linked either by the supply of electron acceptors and donors or by competition for electron acceptors. This review considers both the microbial community related to each process and the technical methods used to measure each process rate. With this background knowledge, this article summarizes how global climate change through increased pCO2, ocean acidification, deoxygenation and anthropogenic N deposition will alter oceanic N cycling, and finally emphasizes the need for comprehensive research on inorganic N transformation in marine ecosystems.

  13. Optimization of microwave-assisted extraction for six inorganic and organic arsenic species in chicken tissues using response surface methodology.

    Science.gov (United States)

    Zhang, Wenfeng; Hu, Yuanan; Cheng, Hefa

    2015-09-01

    Response surface methodology was applied to optimize the parameters for microwave-assisted extraction of six major inorganic and organic arsenic species (As(III), As(V), dimethyl arsenic acid, monomethyl arsenic acid, p-arsanilic acid, and roxarsone) from chicken tissues, followed by detection using a high-performance liquid chromatography with inductively coupled mass spectrometry detection method, which allows the simultaneous analysis of both inorganic and organic arsenic species in the extract in a single run. Effects of extraction medium, solution pH, liquid-to-solid ratio, and the temperature and time of microwave-assisted extraction on the extraction of the targeted arsenic species were studied. The optimum microwave-assisted extraction conditions were: 100 mg of chicken tissue, extracted by 5 mL of 22% v/v methanol, 90 mmol/L (NH4 )2 HPO4 , and 0.07% v/v trifluoroacetic acid (with pH adjusted to 10.0 by ammonium hydroxide solution), ramping for 10 min to 71°C, and holding for 11 min. The method has good extraction performance for total arsenic in the spiked and nonspiked chicken tissues (104.0 ± 13.8% and 91.6 ± 7.8%, respectively), except for the ones with arsenic contents close to the quantitation limits. Limits of quantitation (S/N = 10) for As(III), As(V), dimethyl arsenic acid, monomethyl arsenic acid, p-arsanilic acid, and roxarsone in chicken tissues using this method were 0.012, 0.058, 0.039, 0.061, 0.102, and 0.240 mg/kg (dry weight), respectively.

  14. Spectroscopic characterizations of organic/inorganic nanocomposites

    Science.gov (United States)

    Govani, Jayesh R.

    2009-12-01

    In the present study, pure and 0.3 wt%, 0.4 wt%, as well as 0.5 wt% L-arginine doped potassium dihydrogen phosphate (KDP) crystals were grown using solution growth techniques and further subjected to infrared (IR) absorption and Raman studies for confirmation of chemical group functionalization for investigating the incorporation mechanism of the L-arginine organic material into the KDP crystal structure. Infrared spectroscopic analysis suggests that structural changes are occurring for the L-arginine molecule as a result of its interaction with the KPD crystal. Infrared spectroscopic technique confirms the disturbance of the N-H, C-H and C-N bonds of the amino acid, suggesting successful incorporation of L-arginine into the KDP crystals. Raman analysis also reveals modification of the N-H, C-H and C-N bonds of the amino acid, implying successful inclusion of L-arginine into the KDP crystals. With the help of Gaussian software, a prediction of possible incorporation mechanisms of the organic material was obtained from comparison of the simulated infrared and Raman vibrational spectra with the experimental results. Furthermore, we also studied the effect of L-arginine doping on the thermal stability of the grown KDP crystal by employing Thermo gravimetric analysis (TGA). TGA suggests that increasing the level of L-arginine doping speeds the decomposition process and it weakens the KDP crystal, which indicates successful doping of the KDP crystals with L-arginine amino acid. Urinary stones are one of the oldest and most widely spread diseases in humans, animals and birds. Many remedies have been employed through the ages for the treatment of urinary stones. Recent medicinal measures reflect the modern advances, which are based on surgical removal, percutaneous techniques and extracorporeal shock wave lithotripsy (ESWL). Although these procedures are valuable, they are quite expensive for most people. Furthermore, recurrence of these diseases is awfully frequent with

  15. Syntheses, structures, properties and DFT study of hybrid inorganic-organic architectures constructed from trinuclear lanthanide frameworks and Keggin-type polyoxometalates.

    Science.gov (United States)

    Mirzaei, Masoud; Eshtiagh-Hosseini, Hossein; Lotfian, Nahid; Salimi, Alireza; Bauzá, Antonio; Van Deun, Rik; Decadt, Roel; Barceló-Oliver, Miquel; Frontera, Antonio

    2014-01-28

    In this paper we report the synthesis and X-ray characterization of four novel hybrid inorganic-organic assemblies generated from H4SiW12O40 as Keggin-type polyoxometalates (POM) and, in three of them, a trinuclear lanthanide cluster of type {Na(H2O)3[Ln(HCAM)(H2O)3]3}(4+) is formed, where Ln metal is La in compound 1, Ce in compound 2, and Eu in compound 3 (H3CAM = chelidamic acid or 2,6-dicarboxy-4-hydroxypyridine). These compounds represent the first POM-based inorganic-organic assemblies using chelidamic acid as an organic ligand. The thermal stability of the organic ligand is crucial, since pyridine-2,6-bis(monothiocarboxylate) instead of chelidamic acid is used (compound 4) under the same synthesis conditions, the decomposition of the ligand to pyridine was observed leading to the formation of colorless crystals of a pseudo hybrid inorganic-organic assembly. In compound 4 the hybrid inorganic-organic assembly is not formed and the organic part simply consists of four molecules of protonated pyridine acting as counterions of the [SiW12O40](4-) counterpart. The luminescent properties of compounds and have been investigated and their solid state architectures have been analyzed. Whereas compound only shows ligand emission, the Eu(3+) emission in compound 3 is discussed in detail. We have found that unprecedented anion-π interactions between the POM, which is a tetra-anion, and the aromatic rings play a crucial role in the crystal packing formation. To the best of our knowledge, this is the first report that describes and analyzes this interaction in Keggin-type POM based inorganic-organic frameworks. The energetic features of these interactions in the solid state have been analyzed using DFT calculations in some model systems predicted by us.

  16. Inorganic-organic electrolyte materials for energy applications

    Science.gov (United States)

    Fei, Shih-To

    emphasizes the flammability studies. Chapter 4 expands the application of the ethyleneoxy phosphazene system to dye sensitized solar cell systems, and uses this material as a model for the study of electrode-electrolyte interfaces. We report here the results of our study on polymer electrolyte infiltration and its effect on dye-sensitized solar cells. In-depth studies have been made to compare the effects of different cell assembly procedures on the electrochemical properties as well as infiltration of electrolytes into various electrode designs. The first part of the study is based on the use of thermoplastic phosphazene electrolytes and how the overall fabrication procedure affects electrochemical performance, and the second is the use of cross-section microscopy to characterize the degree of electrolyte infiltration into various nanostructured titanium dioxide electrode surfaces. The results of this study should eventually improve the efficiency and longevity of thermally stable polymer dye solar cell systems. In Chapter 5 the effect of pendant polymer design on methanol fuel cell membrane performance was investigated. A synthetic method is described to produce a proton conductive polymer membrane with a polynorbornane backbone and inorganic-organic cyclic phosphazene pendent groups that bear sulfonic acid units. This hybrid polymer combines the inherent hydrophobicity and flexibility of the organic polymer with the tuning advantages of the cyclic phosphazene to produce a membrane with high proton conductivity and low methanol crossover at room temperature. The ion exchange capacity (IEC), the water swelling behavior of the polymer, and the effect of gamma radiation crosslinking were studied, together with the proton conductivity and methanol permeability of these materials. A typical membrane had an IEC of 0.329 mmolg-1 and had water swelling of 50 wt%. The maximum proton conductivity of 1.13x10 -4 Scm-1 at room temperature is less than values reported for some

  17. Nanostructured organic/inorganic semicondutor photovoltaics: Investigation on morphology and optoelectronics performance

    Science.gov (United States)

    Wanninayake, Aruna Pushpa Kumara

    Organic solar cell is a promising technology because of the versatility of organic materials in terms of tunability of their electrical and optical properties. In addition, their relative insensitivity to film imperfections potentially allows for very low-cost high-throughput roll-to-roll processing. However, the power conversion efficiency of organic solar cell is still limited and needs to be improved in order to be competitive with grid parity. This work is focused on the design and characterization of a new organic/inorganic hybrid device to enhance the efficiency factors of bilayer organic solar cells such as: light absorption, exciton diffusion, exciton dissociation, charge transportation and charge collection at the electrodes. In a hybrid solar cell operation, external quantum efficiency is determined by these five factors. The external quantum efficiency has linear relationship to the power conversation efficiency via short circuit current density. Bulk heterojunction (BHJ) PSCs benefit from a homogeneous donor-acceptor (D-A) contact interface compared to their inorganic counterpart. A homogenous D-A interface offers a longer free path for charge carriers, resulting in a longer diffusional pathway and a larger coulomb interaction between electrons and holes. This is triggered by the low dielectric constant of organic semiconductors. Among various conventional donor-acceptor structures, poly(3-hexylthiophene)/[6,6]-phenyl-C70-butyric acid methyl ester (P3HT/PCBM) mixture is the most promising and ideal donor-acceptor pair due to their unique properties. In order to take benefits from both organic and inorganic materials, inorganic nanoparticles are incorporated in this donor-acceptor polymer structure. Light trapping enhances light absorption and increases efficiencies with thinner device structure. In this study, copper oxide nanoparticles are used in the P3HT/PC70BM active layer to optimize the optical absorption properties in the blend. In addition, zinc

  18. Material Properties of Inorganic Bovine Cancellous Bovine: Nukbone

    Science.gov (United States)

    Piña, Cristina; Palma, Benito; Munguía, Nadia

    2006-09-01

    In this work, inorganic cancellous bovine bone implants prepared in the Instituto de Investigaciones en Materiales — UNAM were characterized. Elementary chemical analysis was made, toxic elements concentration were measured and the content of organic matter also. These implants fulfill all the requirements of the ASTM standards, and therefore it is possible their use in medical applications.

  19. Development of taste sensing system using inorganic membrane

    Science.gov (United States)

    Kojima, Yohichiro; Hasegawa, Yuki

    2011-09-01

    We developed a novel taste sensor for liquid and verified its effectiveness using coffee. We fabricated an inorganic metal oxide membrane liquid sensor using the laser ablation method. The sensor shows a sufficient sensitivity for electrolyte solutions, while it shows a relatively low response for non-electrolyte solutions. We differentiated and identified five brands of commercially available coffee using the sensor.

  20. Applications of Inorganic Chemistry in Biology: An Interdisciplinary Graduate Course

    Science.gov (United States)

    Farrell, Nicholas; Ross, Paul; Roat, Rosette M.

    1998-06-01

    Inorganic chemistry faculty at Virginia Commonwealth University (VCU) are offering an advanced, interdisciplinary, graduate course entitled "Applications of Inorganic Chemistry in Biology". The course utilizes examples from bioinorganic chemistry to introduce advanced topics in synthesis, structural analysis, and analytical methods that are practiced by inorganic chemists. Emphasis is placed on the structure and function of trace and ultratrace transition metals in biological systems and on the use of metals for medicinal purposes. Instrumental techniques such as electron paramagnetic resonance, Mössbauer spectroscopy, and X-ray crystallography are explained in the detail necessary to familiarize students with their use for analysis of bioinorganic systems and their models. Students have take-home examinations during the term and write a term paper describing a metalloprotein whose X-ray structure data is listed in Brookhaven protein data base. The paper follows the same course pattern of classroom discussion of a bioinorganic system, concentrating on the coordination geometry and nearest neighbor contacts of the metal-binding site in the protein, substrate binding site, and relevance to the metalloprotein or enzyme function, mechanism of action of the enzyme or protein, spectroscopic studies on the metal-binding site, and model studies for the protein's metal-binding site. The instructors conclude that their basic goals for the course - introduction to advanced inorganic chemistry topics using bioinorganic examples with emphasis on primary literature sources and computer-assisted displays - are being accomplished.

  1. Multifunctional Inorganic Nanoparticles: Recent Progress in Thermal Therapy and Imaging

    Directory of Open Access Journals (Sweden)

    Kondareddy Cherukula

    2016-04-01

    Full Text Available Nanotechnology has enabled the development of many alternative anti-cancer approaches, such as thermal therapies, which cause minimal damage to healthy cells. Current challenges in cancer treatment are the identification of the diseased area and its efficient treatment without generating many side effects. Image-guided therapies can be a useful tool to diagnose and treat the diseased tissue and they offer therapy and imaging using a single nanostructure. The present review mainly focuses on recent advances in the field of thermal therapy and imaging integrated with multifunctional inorganic nanoparticles. The main heating sources for heat-induced therapies are the surface plasmon resonance (SPR in the near infrared region and alternating magnetic fields (AMFs. The different families of inorganic nanoparticles employed for SPR- and AMF-based thermal therapies and imaging are described. Furthermore, inorganic nanomaterials developed for multimodal therapies with different and multi-imaging modalities are presented in detail. Finally, relevant clinical perspectives and the future scope of inorganic nanoparticles in image-guided therapies are discussed.

  2. Total and inorganic arsenic in fish samples from Norwegian waters

    DEFF Research Database (Denmark)

    Julshamn, K.; Nilsen, B. M.; Frantzen, S.;

    2012-01-01

    of Norway, from 40 positions. The determination of total arsenic was carried out by inductively coupled plasma mass spectrometry following microwave-assisted wet digestion. The determination of inorganic arsenic was carried out by high-performance liquid chromatography–ICP-MS following microwave...

  3. Aromaticity in Polyacene Analogues of Inorganic Ring Compounds

    CERN Document Server

    Chattaraj, P K; Chattaraj, Pratim Kumar; Roy, Debesh Ranjan

    2006-01-01

    The aromaticity in the polyacene analogues of several inorganic ring compounds (BN-acenes, CN-acenes, BO-acenes and Na6-acenes) is reported here for the first time. Conceptual density functional theory based reactivity descriptors and the nucleus independent chemical shift (NICS) values are used in this analysis.

  4. Facile synthesis of zirconia doped hybrid organic inorganic silica membranes

    NARCIS (Netherlands)

    Hove, ten M.; Nijmeijer, A.; Winnubst, A.J.A.

    2015-01-01

    Hybrid organic inorganic silica membranes are interesting candidates for gas-separation applications due to their excellent hydrothermal stability. However, up to now these membranes lack the separation performance required to separate hydrogen from carbon dioxide. In this work a procedure for dopin

  5. Nanoscale in Wood, Nanowood and Wood-Inorganic Nanocomposites

    Institute of Scientific and Technical Information of China (English)

    Zhao Guangjie; Lu Wenhua

    2003-01-01

    In order to introduce nano science and technology (NST) into the research field of wood science and technology, andpromote the research of wood science and wood-inorganic composites to nanoscale, some new concepts, such as the nano space inwood, nano structure units of wood and nanowood are put forward in this paper based on the layer structure of wood cell wall and thepile-up model of its main components. Furthermore, the process of preparing nanowood is discussed, and wood-inorganic nanocom-posites may be operated in three ways with wood (matrix) and inorganic filler phase in 0-2, 0-3 or 2-3 dimensions respectively. Thefollowing results are obtained: (1) The nanoscale voids in wood indicate that wood has inherent space to accommodate nanosizedmaterials, such as nanoparticles, nanotubes and nanosticks; (2) According to the size from top down, the nano structure units in woodcan be classified as: nanolayers, nano CMF (cellulose microfibril) and matrix, nano crystallite units and cellulose chain clusters, andthese can theoretically form nanowood; (3) The preparation of wood-inorganic nanocomposites can be operated on 0-2, 0-3 or 2-3dimensions.

  6. An all-inorganic polyoxometalate–polyoxocation chemical garden

    OpenAIRE

    Points, Laurie J.; Cooper, Geoffrey J.T.; Dolbecq, Anne; Mialane, Pierre; Cronin, Leroy

    2016-01-01

    Herein, we show it is possible to produce wholly inorganic chemical gardens from a cationic polyoxometalate (POM) seed in an anionic POM solution, demonstrating a wholly POM-based chemical garden system that produces architectures over a wide concentration range. Six concentration dependent growth regimes have been discovered and characterized: clouds, membranes, slugs, tubes, jetting and budding.

  7. An all-inorganic polyoxometalate-polyoxocation chemical garden.

    Science.gov (United States)

    Points, Laurie J; Cooper, Geoffrey J T; Dolbecq, Anne; Mialane, Pierre; Cronin, Leroy

    2016-01-31

    Herein, we show it is possible to produce wholly inorganic chemical gardens from a cationic polyoxometalate (POM) seed in an anionic POM solution, demonstrating a wholly POM-based chemical garden system that produces architectures over a wide concentration range. Six concentration dependent growth regimes have been discovered and characterized: clouds, membranes, slugs, tubes, jetting and budding.

  8. Determination of some electrical parameters for composite inorganic membranes

    Energy Technology Data Exchange (ETDEWEB)

    Benavente, J.; Ramos-Barrado, J.R.; Cabeza, A. [Universidad de Malaga (Spain)

    1994-12-31

    Composite inorganic membranes were obtained by deposition of an inorganic precipitate layer (uranyl phosphonate: UO{sub 2}(O{sub 3}PC{sub 6}H{sub 5}) or UPP) on a commercial porous alumina membrane (Anopore{trademark}, 0.2 {mu}m pore size). Salt diffusion and membrane potential for the whole membrane were measured for NaCl and other electrolytes containing the precipitate generating ions, and for concentration ranging between 10{sup -4}M and 210{sup -2}M. Dielectric parameters (resistance and capacitance) were obtained from impedance spectroscopy measurements, and the equivalent circuits associated to the membrane/electrolyte systems were also determined. From the experimental results, other parameters such as cation transport numbers and ionic permeabilities were obtained. Concentration dependence of all these parameters was also considered. Measurements were carried out with the composite inorganic membrane and the alumina porous support. A comparison of the results found for both membranes gives information about the value of all these parameters in the layer formed by the inorganic UPP precipitate.

  9. Inorganic porous hollow fiber membranes : with tunable small radial dimensions

    NARCIS (Netherlands)

    Luiten-Olieman, M.W.J.

    2012-01-01

    The objectives of this thesis are twofold. The first aim is to develop of robust coating procedures for thin supported films onto porous ceramic supports. The second aim is the development of a preparation methodology for high quality porous inorganic membranes, with large membrane surface area. A r

  10. Identification of novel rice low phytic acid mutations via TILLING by sequencing

    Science.gov (United States)

    Phytic acid (myo-inositol-1,2,3,4,5,6-hexakisphosphate or InsP6) accounts for 75-85% of the total phosphorus in seeds. Low phytic acid (lpa) mutants exhibit decreases in seed InsP6 with corresponding increases in inorganic P which, unlike phytic acid P, is readily utilized by humans and monogastric ...

  11. Mössbauer study of the inorganic sulfur removal from coals

    Science.gov (United States)

    Reyes Caballero, F.; Martínez Ovalle, S. A.

    2014-01-01

    Mössbauer Spectroscopy (MS) was applied to study the occurrence and behavior of the iron-sulfur-containing minerals in coal and coal fractions obtained by different separation methods: hydrocyclonic, flotation and chemical removal process. Samples of one high sulfur coal from Guachinte mine (Valle, Colombia) and three low sulfur coals from the El Salitre zone (Paipa-Boyacá, Colombia) were analyzed. MS evidenced only the presence of pyrite in Esmeralda and Las Casitas coals, while it identified pyrite and siderite on Cerezo coal. MS and SEM- EDX confirm the inorganic sulfur removal on Guachinte coal submitted to hydrocyclonic removal process. MS of the precipitated coal fraction from Las Casitas mine obtained by flotation in water showed the presence of ferrous sulfate because of coal-weathering process. Treatment with hot diluted HNO3 equal to 27 acid on raw coal sample from Las Casitas mine showed that almost all of the pyrite in raw coal was removed.

  12. A classification and regression tree model of controls on dissolved inorganic nitrogen leaching from European forests.

    Science.gov (United States)

    Rothwell, James J; Futter, Martyn N; Dise, Nancy B

    2008-11-01

    Often, there is a non-linear relationship between atmospheric dissolved inorganic nitrogen (DIN) input and DIN leaching that is poorly captured by existing models. We present the first application of the non-parametric classification and regression tree approach to evaluate the key environmental drivers controlling DIN leaching from European forests. DIN leaching was classified as low (15kg N ha(-1) year(-1)) at 215 sites across Europe. The analysis identified throughfall NO(3)(-) deposition, acid deposition, hydrology, soil type, the carbon content of the soil, and the legacy of historic N deposition as the dominant drivers of DIN leaching for these forests. Ninety four percent of sites were successfully classified into the appropriate leaching category. This approach shows promise for understanding complex ecosystem responses to a wide range of anthropogenic stressors as well as an improved method for identifying risk and targeting pollution mitigation strategies in forest ecosystems.

  13. Experimental data of inorganic gel based smart window using silica sol–gel process

    Directory of Open Access Journals (Sweden)

    Dayeon Jung

    2016-12-01

    Full Text Available In this article experimental data are presented for inorganic gel based smart window fabricated using silica sol–gel process. Parallel beam transmittances were measured as functions of voltages for samples fabricated with different concentrations of nitric acid. Spectroscopic transmittance data at different driving voltages for samples fabricated with different LC concentrations are shown. Transmittance spectra of the Si–Ti based gel-based-liquid-crystal (GDLC device measured as different driving voltages were compared with those of PDLC. GDLC showed much lower operating voltages, 10–15 V, for on-state. Formation of the LC droplet in gelation process is illustrated. The methyl organic group surrounds LC droplets. Demonstration of GDLC based smart window showed the successful operation with low driving voltages. GDLC window shows clear color, even at off-state, compared with PDLC.

  14. Comparison of histological and ultrastructural changes in mice organs after supplementation with inorganic and organic selenium.

    Science.gov (United States)

    Tos-Luty, Sabina; Obuchowska-Przebirowska, Daniela; Latuszynska, Jadwiga; Musik, Irena; Tokarska-Rodak, Malgorzata

    2003-01-01

    Two organic compounds of selenium, 4-o-totyl-selenosemicarbazide p-chlorobenzoic acid (chain compound) produced at the Chemistry Department of the University Medical School in Lublin, and one inorganic compound of sodium IV selenite (Na(2)SeO(3)) were used. The preparations were used per os in doses of 1 mg/kg body weight and 0.5 mg/kg body weight. The studies were conducted on female Swiss mice, covering seven groups of animals, i.e. 6 experimental and 1 control. Histopathologic changes were observed in liver, kidney, lung and heart. Ultrastructural changes were observed in liver and kidney. Our studies indicate a dose-dependent effect of selenium on histopathologic and ultrastructural changes. It is possible therefore, that the extent of excess of selenium exerts a greater influence on a cell than the form of supplemented selenium.

  15. Inorganic-organic hybrids originating from organosilane anchored onto leached vermiculite

    Directory of Open Access Journals (Sweden)

    Ana P. M. Alves

    2013-01-01

    Full Text Available The reactivity of clay minerals leached in grafting reactions was investigated. Precursor solids were prepared by treating the sodium vermiculites with nitric acid solutions at several concentrations. The lixiviation produced the restructured porous solids with surface area over a wide range, varying from 133 to 673 m² g- 1. The sodium and lixiviated vermiculites reacted covalently with silylating agent, 3-aminopropyltrimethoxysilane, to attach this agent onto the inorganic surface, through the free available silanols. The products were characterized by CNH elemental analysis, infrared spectroscopy, X-ray diffraction, nuclear magnetic resonance in the solid state for carbon and silicon. CHN data expressed by significant contents of anchored organic chains, up to 2.14 mmol g- 1, as the degree of leaching was increased. The success of this investigation is directly related to the leaching of the natural vermiculite, which is strongly influenced by the reactivity of the abundant original source.

  16. Evaluation of inorganic matrixes as supports for immobilization of microbial lipase

    Directory of Open Access Journals (Sweden)

    Castro H.F.

    2000-01-01

    Full Text Available Candida rugosa was immobilized by physical adsorption on several inorganic supports using hexane as coupling medium. The enzymatic activities of the different derivatives were determined by both hydrolysis of olive oil and esterification of n-butanol with butyric acid. The results were compared to previous data obtained by using a controlled porous silica matrix. The goal was to contribute in searching inexpensive supports for optimum lipase performance. All supports examined exhibited good properties for binding the enzyme lipase. Zirconium phosphate was the best support, giving the highest percentage of protein fixation (86% and the highest retention of lipase activity after immobilization (34%. The operational stability performance for niobium oxide derivative was improved by previously activated the support with silane and glutaraldehyde. Thermal stabilities were also examined by thermal gravimetric analysis (TG.

  17. Inorganic-Organic Hybrid 18-Molybdodiphosphate Nanoparticles Bulk-modified Carbon Paste Electrode and Its Electrocatalysis

    Institute of Scientific and Technical Information of China (English)

    WANG,Xiu-Li(王秀丽); KANG,Zhen-Hui(康振辉); WANG,En-Bo(王恩波); HU,Chang-Wen(胡长文)

    2002-01-01

    A kind of inorganic- organic hybrid 18-molybdodiphosphate nanoparticles ([(C4H9)4N]6P2Mo18O62 @4H2O) was firstly used as a bulk-modifier to fabricate a three-dimensional chemically modified carbon paste electrode (CPE) by direct mixing. The electrochemical behavior of the solid nanoparticles dispersed in the CPE in acidic aqueous solution was characterized by cyclic and square-wave voltammetry. The hybrid 18-molybdodiphosphate nanoparticles bulk-modified CPE (MNP-CPE) displayed a high electrocatalytic activity towards the reduction of nitrite,bromate and hydrogen peroxide. The remarkable advantages of the MNP-CPE over the traditional polyoxometalates-modified electrodes are their excellent reproducibility of surface-renewal and high stability owing to the insolubility of the hybrid 18-molybdodiphosphate nanoparticles.

  18. Preparation and Performance Analysis of Inorganic Polymer Flocculant PZFSiC

    Institute of Scientific and Technical Information of China (English)

    GAN Li; MENG Zhao-ping; Pan Jie-nan

    2004-01-01

    A new inorganic polymer flocculant-PZFSiC (zinc-iron-silicate polymer composite) is prepared by adding acid into a high modulus solution of water glass and introducing appropriate metallic ions(M) including Zn and Fe. The influence on flocculability of factors such as the mole ratios of M to SiO2,stirring time and pH are discussed .And the optimal preparing technical parameters are obtained by orthogonal tests. The optimum technical conditions of flocculation are determined. The result shows that when less PZFSiC is added into troubled water or waste water, turbidity removal can hit 98%, COD removal can exceed 93%. The water sample treated is clear and of good quality. These results also indicate that PZFSiC is a highly effective, nontoxic and benign to the enviroment.

  19. Role of long-range intermolecular forces in the formation of inorganic nanoparticle clusters.

    Science.gov (United States)

    Gibbs, G V; Crawford, T D; Wallace, A F; Cox, D F; Parrish, R M; Hohenstein, E G; Sherrill, C D

    2011-11-17

    An understanding of the role played by intermolecular forces in terms of the electron density distribution is fundamental to the understanding of the self-assembly of molecules in the formation of a molecular crystal. Using ab initio methods capable of describing both short-range intramolecular interactions and long-range London dispersion interactions arising from electron correlation, analyses of inorganic dimers of As(4)S(4) and As(4)O(6) molecules cut from the structures of realgar and arsenolite, respectively, reveal that the molecules adopt a configuration that closely matches that observed for the crystal. Decomposition of the interaction energies using symmetry-adapted perturbation theory reveals that both model dimers feature significant stabilization from electrostatic forces as anticipated by a Lewis acid/Lewis base picture of the interaction. London dispersion forces also contribute significantly to the interaction, although they play a greater role in the realgar structure near equilibrium than in arsenolite.

  20. Inorganic chemistry of defensive peroxidases in the human oral cavity.

    Science.gov (United States)

    Ashby, M T

    2008-10-01

    The innate host response system is comprised of various mechanisms for orchestrating host response to microbial infection of the oral cavity. The heterogeneity of the oral cavity and the associated microenvironments that are produced give rise to different chemistries that affect the innate defense system. One focus of this review is on how these spatial differences influence the two major defensive peroxidases of the oral cavity, salivary peroxidase (SPO) and myeloperoxidase (MPO). With hydrogen peroxide (H(2)O(2)) as an oxidant, the defensive peroxidases use inorganic ions to produce antimicrobials that are generally more effective than H(2)O(2) itself. The concentrations of the inorganic substrates are different in saliva vs. gingival crevicular fluid (GCF). Thus, in the supragingival regime, SPO and MPO work in unison for the exclusive production of hypothiocyanite (OSCN(-), a reactive inorganic species), which constantly bathes nascent plaques. In contrast, MPO is introduced to the GCF during inflammatory response, and in that environment it is capable of producing hypochlorite (OCl(-)), a chemically more powerful oxidant that is implicated in host tissue damage. A second focus of this review is on inter-person variation that may contribute to different peroxidase function. Many of these differences are attributed to dietary or smoking practices that alter the concentrations of relevant inorganic species in the oral cavity (e.g.: fluoride, F(-); cyanide, CN(-); cyanate, OCN(-); thiocyanate, SCN(-); and nitrate, NO(3)(-)). Because of the complexity of the host and microflora biology and the associated chemistry, it is difficult to establish the significance of the human peroxidase systems during the pathogenesis of oral diseases. The problem is particularly complex with respect to the gingival sulcus and periodontal pockets (where the very different defensive stratagems of GCF and saliva co-mingle). Despite this complexity, intriguing in vitro and in vivo

  1. Biomolecular Modification of Inorganic Crystal Growth

    Energy Technology Data Exchange (ETDEWEB)

    De Yoreo, J J

    2007-04-27

    The fascinating shapes and hierarchical designs of biomineralized structures are an inspiration to materials scientists because of the potential they suggest for biomolecular control over materials synthesis. Conversely, the failure to prevent or limit tissue mineralization in the vascular, skeletal, and urinary systems is a common source of disease. Understanding the mechanisms by which organisms direct or limit crystallization has long been a central challenge to the biomineralization community. One prevailing view is that mineral-associated macromolecules are responsible for either inhibiting crystallization or initiating and stabilizing non-equilibrium crystal polymorphs and morphologies through interactions between anionic moieties and cations in solution or at mineralizing surfaces. In particular, biomolecules that present carboxyl groups to the growing crystal have been implicated as primary modulators of growth. Here we review the results from a combination of in situ atomic force microscopy (AFM) and molecular modeling (MM) studies to investigate the effect of specific interactions between carboxylate-rich biomolecules and atomic steps on crystal surfaces during the growth of carbonates, oxalates and phosphates of calcium. Specifically, we how the growth kinetics and morphology depend on the concentration of additives that include citrate, simple amino acids, synthetic Asp-rich polypeptides, and naturally occurring Asp-rich proteins found in both functional and pathological mineral tissues. The results reveal a consistent picture of shape modification in which stereochemical matching of modifiers to specific atomic steps drives shape modification. Inhibition and other changes in growth kinetics are shown to be due to a range of mechanisms that depend on chemistry and molecular size. Some effects are well described by classic crystal growth theories, but others, such as step acceleration due to peptide charge and hydrophylicity, were previously unrealized

  2. Enzyme Mechanism and Slow-Onset Inhibition of Plasmodium falciparum Enoyl-Acyl Carrier Protein Reductase by an Inorganic Complex

    Science.gov (United States)

    de Medeiros, Patrícia Soares de Maria; Ducati, Rodrigo Gay; Basso, Luiz Augusto; Santos, Diógenes Santiago; da Silva, Luiz Hildebrando Pereira

    2011-01-01

    Malaria continues to be a major cause of children's morbidity and mortality worldwide, causing nearly one million deaths annually. The human malaria parasite, Plasmodium falciparum, synthesizes fatty acids employing the Type II fatty acid biosynthesis system (FAS II), unlike humans that rely on the Type I (FAS I) pathway. The FAS II system elongates acyl fatty acid precursors of the cell membrane in Plasmodium. Enoyl reductase (ENR) enzyme is a member of the FAS II system. Here we present steady-state kinetics, pre-steady-state kinetics, and equilibrium fluorescence spectroscopy data that allowed proposal of P. falciparum ENR (PfENR) enzyme mechanism. Moreover, building on previous results, the present study also evaluates the PfENR inhibition by the pentacyano(isoniazid)ferrateII compound. This inorganic complex represents a new class of lead compounds for the development of antimalarial agents focused on the inhibition of PfENR. PMID:21603269

  3. Chemistry and applications of inorganic-organic polymers : organically modified silicates

    OpenAIRE

    Schmidt, Helmut K.; Seiferling, Bernhard

    1986-01-01

    The conbination of inorganic polymeric networks with organic components leads ot inorganic-organic polymers. A convenient method for the introduction of organic radials into an inorganic backbone is the use of aorganosubstituted silico esters in a polycondensation process. This leads to ≡Si-O-Si≡ network containing materials, so-called organically modified silicates (ORMOSILs). For the synthesis of the inorganic backbone, in opposition to the high temperature preparation of non-me...

  4. Prediction Model of Antibacterial Activities for Inorganic Antibacterial Agents Based on Artificial Neural Networks

    Institute of Scientific and Technical Information of China (English)

    刘雪峰; 张利; 涂铭旌

    2004-01-01

    Quantitatively evaluation of antibacterial activities of inorganic antibacterial agents is an urgent problem to be solved. Using experimental data by an orthogonal design, a prediction model of the relation between conditions of preparing inorganic antibacterial agents and their antibacterial activities has been developed. This is accomplished by introducing BP artificial neural networks in the study of inorganic antibacterial agents..It provides a theoretical support for the development and research on inorganic antibacterial agents.

  5. Soft templating strategies for the synthesis of mesoporous materials: inorganic, organic-inorganic hybrid and purely organic solids.

    Science.gov (United States)

    Pal, Nabanita; Bhaumik, Asim

    2013-03-01

    With the discovery of MCM-41 by Mobil researchers in 1992 the journey of the research on mesoporous materials started and in the 21st century this area of scientific investigation have extended into numerous branches, many of which contribute significantly in emerging areas like catalysis, energy, environment and biomedical research. As a consequence thousands of publications came out in large varieties of national and international journals. In this review, we have tried to summarize the published works on various synthetic pathways and formation mechanisms of different mesoporous materials viz. inorganic, organic-inorganic hybrid and purely organic solids via soft templating pathways. Generation of nanoscale porosity in a solid material usually requires participation of organic template (more specifically surfactants and their supramolecular assemblies) called structure-directing agent (SDA) in the bottom-up chemical reaction process. Different techniques employed for the syntheses of inorganic mesoporous solids, like silicas, metal doped silicas, transition and non-transition metal oxides, mixed oxides, metallophosphates, organic-inorganic hybrids as well as purely organic mesoporous materials like carbons, polymers etc. using surfactants are depicted schematically and elaborately in this paper. Moreover, some of the frontline applications of these mesoporous solids, which are directly related to their functionality, composition and surface properties are discussed at the appropriate places.

  6. Toward High-Performance Organic-Inorganic Hybrid Solar Cells: Bringing Conjugated Polymers and Inorganic Nanocrystals in Close Contact.

    Science.gov (United States)

    He, Ming; Qiu, Feng; Lin, Zhiqun

    2013-06-06

    Organic-inorganic hybrid solar cells composed of conjugated polymers (CPs) and inorganic nanocrystal (NC) semiconductors have garnered considerable attention as a potential alternative to traditional silicon solar cells due to the capacity of producing high-efficiency solar energy in a cost-effective manner. The combination of advantageous characteristics of CPs and NCs enables the construction of nanostructured high-performance, lightweight, flexible, large-area, and low-cost hybrid solar cells. However, it remains a grand challenge to control the film morphology and interfacial structure of such organic/inorganic semiconductor blends on the nanoscale. In this Perspective, we highlight the strategies of implementing close contact between CPs and NCs by tailoring the colloidal synthesis, the coordination reaction, and the chemical modification of CPs. As such, they offer promising opportunities for rationally controlling the phase separation between electron-donating CPs and electron-accepting NCs, increasing the interfacial areas between them, enhancing their electronic interaction, and thus substantially promoting the photovoltaic performance of the resulting organic-inorganic hybrid solar cells.

  7. Inorganic oxides with mesoporosity or combined meso-and microporosity and process for the preparation thereof

    NARCIS (Netherlands)

    Shan, Z; Maschmeyer, T; Jansen, J.C.

    2001-01-01

    Bimodal inorganic material that in a pore size distribution plot has distinct mesopore and micropore peaks. A process for producing a bimodal material or a material that contains essentially only mesopores involves heating an inorganic oxide in the presence of material that bonds to the inorganic ox

  8. Utilization of a diol-stationary phase column in ion chromatographic separation of inorganic anions.

    Science.gov (United States)

    Arai, Kaori; Mori, Masanobu; Kozaki, Daisuke; Nakatani, Nobutake; Itabashi, Hideyuki; Tanaka, Kazuhiko

    2012-12-28

    We describe the ion chromatographic separation of inorganic anions using a diol-stationary phase column (-CH(OH)CH(2)OH; diol-column) without charged functional groups. Anions were separated using acidic eluent as in typical anion-exchange chromatography. The retention volumes of anions on the diol-column increased with increasing H(+) concentration in the eluent. The anion-exchange capacities of diol-columns in the acidic eluent (pH 2.8) were larger than that of zwitterionic stationary phase column but smaller than that of an anion-exchange column. The separation of anions using the diol-column was strongly affected by the interaction of H(+) ions with the diol-functional groups and by the types of the eluents. In particular, the selection of the eluent was very important for controlling the retention time and resolution. Good separation was obtained using a diol-column (HILIC-10) with 5 mM phthalic acid as eluent. The limits of detection at a signal-to-noise ratio of 3 ranged from 1.2 to 2.7 μM with relative standard deviations (RSD, n=5) of 0.04-0.07% for the retention time and 0.4-2.0% for the peak areas. This method was successfully applied to the determination of H(2)PO(4)(-), Cl(-), and NO(3)(-) in a liquid fertilizer sample.

  9. Environmental impact of hazardous inorganic materials. Pollution and remediation of soils

    Energy Technology Data Exchange (ETDEWEB)

    Tokunaga, S.; Hakuta, T. [National Institute of Materials and Chemical Research, Tsukuba (Japan); Barrington, S.; Wasay, S. [McGill University, (Canada)

    1998-02-10

    Recently, soil pollution has become a grave social problem. This paper reviews history, laws and regulations, current status and measures related to soil pollution, centered by those of Japan. Soil pollution problems in Japan date back to around 1880, when pollution of the Watarase River basin started by waste water exhausted from Asio Mine. Various grave problems have been recorded since then, including the Itai-itai and Minamata Diseases caused by Cd and methyl mercury, respectively, which started in 1945 and 1956, with the result that the government has amended laws/regulations related to treatment and cleaning of industrial wastes. Later, the related laws/regulations have been frequently amended, and the environmental standards related to soil pollution was established in 1991. Treatment for remediation of polluted soils has been effected with the aid of inorganic acids, organic solvents, chelating agents, natural organic acids (such as acetic and formic acids) and biological surface active agents. They must be carefully planned to take into consideration various aspects, such as pH level and other conditions, cost and environmental safety, before being actually used. One of the recommended measures is on-the-site treatment in an enclosed space while regenerating and recycling the agent. 66 refs., 7 figs., 8 tabs.

  10. Improving phosphorus availability in an acid soil using organic amendments produced from agroindustrial wastes.

    Science.gov (United States)

    Ch'ng, Huck Ywih; Ahmed, Osumanu Haruna; Majid, Nik Muhamad Ab

    2014-01-01

    In acid soils, soluble inorganic phosphorus is fixed by aluminium and iron. To overcome this problem, acid soils are limed to fix aluminium and iron but this practice is not economical. The practice is also not environmentally friendly. This study was conducted to improve phosphorus availability using organic amendments (biochar and compost produced from chicken litter and pineapple leaves, resp.) to fix aluminium and iron instead of phosphorus. Amending soil with biochar or compost or a mixture of biochar and compost increased total phosphorus, available phosphorus, inorganic phosphorus fractions (soluble inorganic phosphorus, aluminium bound inorganic phosphorus, iron bound inorganic phosphorus, redundant soluble inorganic phosphorus, and calcium bound phosphorus), and organic phosphorus. This was possible because the organic amendments increased soil pH and reduced exchangeable acidity, exchangeable aluminium, and exchangeable iron. The findings suggest that the organic amendments altered soil chemical properties in a way that enhanced the availability of phosphorus in this study. The amendments effectively fixed aluminium and iron instead of phosphorus, thus rendering phosphorus available by keeping the inorganic phosphorus in a bioavailable labile phosphorus pool for a longer period compared with application of Triple Superphosphate without organic amendments.

  11. Improving Phosphorus Availability in an Acid Soil Using Organic Amendments Produced from Agroindustrial Wastes

    Directory of Open Access Journals (Sweden)

    Huck Ywih Ch’ng

    2014-01-01

    Full Text Available In acid soils, soluble inorganic phosphorus is fixed by aluminium and iron. To overcome this problem, acid soils are limed to fix aluminium and iron but this practice is not economical. The practice is also not environmentally friendly. This study was conducted to improve phosphorus availability using organic amendments (biochar and compost produced from chicken litter and pineapple leaves, resp. to fix aluminium and iron instead of phosphorus. Amending soil with biochar or compost or a mixture of biochar and compost increased total phosphorus, available phosphorus, inorganic phosphorus fractions (soluble inorganic phosphorus, aluminium bound inorganic phosphorus, iron bound inorganic phosphorus, redundant soluble inorganic phosphorus, and calcium bound phosphorus, and organic phosphorus. This was possible because the organic amendments increased soil pH and reduced exchangeable acidity, exchangeable aluminium, and exchangeable iron. The findings suggest that the organic amendments altered soil chemical properties in a way that enhanced the availability of phosphorus in this study. The amendments effectively fixed aluminium and iron instead of phosphorus, thus rendering phosphorus available by keeping the inorganic phosphorus in a bioavailable labile phosphorus pool for a longer period compared with application of Triple Superphosphate without organic amendments.

  12. New inorganic membranes for pervaporation. Preparation and first results

    Energy Technology Data Exchange (ETDEWEB)

    Van Veen, H.M.; Vente, J.F.; Wolfs, D.P.; Kreiter, R.; Pex, P.P.A.C. [ECN Energy Efficiency in the Industry, Petten (Netherlands)

    2006-08-15

    The expected high chemical and thermal stability of inorganic membranes compared to polymer membranes has resulted in a growing research activity with the aim of replacing polymer membranes with inorganic ones. The superior separation performance, i.e. selectivity and flux, of silica-based membranes in the dehydration of alcohols and solvents at elevated temperatures has raised the interest even further. High flux performance is required especially to overcome the higher unit cost price of the inorganic membranes. It is proven that the required water flux of at least 3 kg/m{sup 2}.h, for the dehydration of 5wt.% water in butanol as a representative standard application, can be achieved easily. The profitable application of inorganic membranes depends also on a reliable, stable long-term behaviour. Unfortunately, information on this topic is still very limited. Dehydration experiments at temperatures below 100C indicate a fast decrease of the water flux through silica membranes during the first few days of operation. The origin of this decline has not been determined yet, but we believe that sorption processes on the membrane surface play an important role. In an attempt to overcome this fast decline, we have prepared methylated silica (Me-SiO2) membranes. By incorporating methyl groups in the silica structure, the water flux decline during the first weeks is only in the order of 20% and is stable hereafter. Dehydration experiments performed up to 165C using these Me-SiO2 membranes showed membrane failure after 4 to 40 days due to reorganisation of the silica structure. In all cases we observe a strong increase in the organic flux, indicating that the pore size increases over time. As a consequence, we conclude that the application window of state-of-the-art Me-SiO2 membranes for use in dehydration processes is limited to 95C. Microporous titania, zirconia and organic/inorganic hybrid silica materials are expected to have a much higher hydrothermal stability than

  13. Unique roles of acidic amino acids in phase transformation of calcium phosphates.

    Science.gov (United States)

    Chu, Xiaobin; Jiang, Wenge; Zhang, Zhisen; Yan, Yang; Pan, Haihua; Xu, Xurong; Tang, Ruikang

    2011-02-10

    Although phase transformation is suggested as a key step in biomineralization, the chemical scenario about how organic molecules mediate inorganic phase transformations is still unclear. The inhibitory effect of amino acids on hydroxyapatite (HAP, the main inorganic component of biological hard tissues such as bone and enamel) formation was concluded by the previous biomimetic modeling based upon direct solution crystallization. Here we demonstrate that acidic amino acids, Asp and Glu, could promote HAP crystallization from its precursor crystal, brushite (DCPD). However, such a promotion effect could not be observed when the nonacidic amino acids were applied in the transformation-based HAP formation. We found that the specific modification of acidic amino acid on crystal-solution interfaces played a key role in the phase transition. The distinct properties between DCPD and HAP in the solution resulted in an interfacial energy barrier to suppress the spontaneous formation of HAP phase on DCPD phase. Different from the other amino acids, the carboxylate-rich amino acids, Asp and Glu, could modify the interfacial characteristics of these two calcium phosphate crystals to make them similar to each other. The experiments confirmed that the involvement of Asp or Glu reduced the interfacial energy barrier between DCPD and HAP, leading to a trigger effect on the phase transformation. An in-depth understanding about the unique roles of acidic amino acids may contribute to understanding phase transformation controls druing biomineralization.

  14. Organic and inorganic fertilization effects on DTPA-extractable Fe, Cu, Mn and Zn, and their concentration in the edible portion of crops

    OpenAIRE

    Maqueda Porras, Celia; Herencia, Juan F.; Ruiz Porras, J. C.; Hidalgo García, Mª F.

    2011-01-01

    The application of organic composts to soil may affect the availability of micronutrients and their concentration in plants. The present field research study compared soil micronutrient extractability after 5 years of organic fertilization v. conventional inorganic fertilization. Iron (Fe), copper (Cu), manganese (Mn) and zinc (Zn) were extracted from soil using diethylene triamine pentaacetic acid (DTPA) and the data obtained were compared with the concentration of these micronutrients in th...

  15. 过氧乙酸破解和化学重絮凝改善活性污泥过滤脱水性能%Enhancement of activated sludge dewatering performance with combined peroxyacetic acid oxiution and chemical re?flocculation with inorganic coagulants

    Institute of Scientific and Technical Information of China (English)

    曹秉帝; 张伟军; 王东升; 段晋明

    2016-01-01

    Extracellular polymeric substances ( EPS) in sewage sludge are highly hydrophilic, and the destruction of EPS structure is very essential for the high-performance dewatering process. In this study, the peracetic acid lysis and chemical re-flocculation was used to achieve the volume reduction and dewaterability improvement of waste activated sludge. Moreover, dynamic variations of the floc morphology and EPS properties of sludge were also investigated. The results indicated that PAA treatment had very limited effect on sludge filterability, while filtration drying performance was effectively improved. PAA could effectively solubilize the sludge particle and destroy the protein-like substances, resulting in an efficient releasing of bound water. Sludge dewatering was enhanced under a low pH level after PAA oxiution, ascribing to the higher oxiutive ability of PAA under acid conditions. No integral sludge floc could be observed after PAA treatment at high dosages. Floc reformed after the additive of PAC and ferric chloride, meanwhile both filterability and dewaterability were improved. Furthermore, PAC performed better in improving sludge dewatering performance than ferric chloride due to its high adsorption and bridging abilities.%活性污泥中的胞外聚合物( EPS)高度亲水,破坏EPS结构是促使结合水释放的必要过程.为此,研究利用过氧乙酸( PAA)预氧化破解污泥和化学絮凝过程以同步实现污泥减量和脱水性改善,深入解析组合调理过程中污泥絮体形态特征及EPS分布和组成的变化特征.结果表明:PAA处理污泥对其过滤特性影响不大,但有效降低滤后泥饼的含水率;PAA能够有效破解污泥,破坏EPS中蛋白质类有机物,促使结合水释放;随着pH的降低,PAA对污泥脱水性的改善效果更佳,这主要是因为酸性环境有效提高了PAA对污泥 EPS的氧化效率;高剂量 PAA 处理污泥后未见到有完整结构的絮体.投加聚合氯化铝( PAC)和氯化铁

  16. Preparation and Thermal Properties of Fatty Acid/Inorganic Nano-particle Form-Stable Phase Change Material%脂肪酸/无机纳米颗粒基定形相变材料的制备与热性能

    Institute of Scientific and Technical Information of China (English)

    孟多; 王立久

    2013-01-01

    以工业水玻璃为纳米SiO2前驱物,以癸酸(CA)和月桂酸(LA)二元低共熔酸为相变芯材,在表面活性剂的参与下,采用溶胶-凝胶法一步制备出纳米级复合定形相变蓄热材料.利用透射电子显微镜,扫描电子显微镜,傅里叶红外光谱仪,方差扫描量热法和热重分析等测试技术对此定形相变蓄热材料的结构和性能进行分析,并采用瞬态热线法测量了其导热系数.结果表明:相变芯材在吸热熔化后不会产生流动和渗漏;复合相变材料中脂肪酸含量(质量分数)为46%,具有良好的相变蓄热性能(相变温度19.57℃,相变潜热71.28 J/g)和热稳定性;复合相变材料导热系数为0.178 W/(m·K),可作为一种良好的隔热、保温建筑材料.%A kind of form-stable phase change material (PCM) based on capric-lauric acid eutectic acting as the heat-absorbing material and nano silicon dioxide serving as the supportive material was prepared by sol-gel method. The morphology, chemical characteristics and thermal properties of the composite PCM were investigated by transmission electron microscopy(TEM), scanning electron microscopy (SEM), and Fourier-transform infrared (FT-IR), differential scanning calorimetry(DSC) and thermogravimetric analysis (TGA). The results indicate that fatty acid eutectic can be immobilized in the three-dimensional network structure when the composite PCM is heated to above the phase change temperature. The proportion of the CA-LA eutectic in the composite PCM is 46%(by mass). The phase change temperature and latent heat of the composite PCM were determined as 19. 57 °C and 71. 28 J/g, respectively. Mean-while, thermal conductivity of the composite was measured to be 0. 178 W/(m · K) by using the transient hot-wire method. Thus it can be applied for energy conservation as the thermal insulation material.

  17. L-缬氨酸产生菌JVHK597的选育及无机盐对其产酸量的影响%Breeding of of L-valine Producing Strain JVHK597 and Influence of Inorganic Salt on Its Acid Production

    Institute of Scientific and Technical Information of China (English)

    刘焕民; 葛向阳; 张伟国

    2011-01-01

    [目的]筛选L-缬氨酸高产菌株并研究其发酵条件.[方法]以黄色短杆菌(Brebvibacterium flavum)突变株ZGH61.28为出发菌株,采用紫外线(UV)、硫酸二乙酯(DES)和亚硝基胍(NTG)3种诱变剂进行诱变处理,通过摇瓶培养筛选出L-缬氨酸高产突变菌株.[结果]经过UV、DES和NTG3种诱变剂处理菌株ZGH6128,逐步获得菌株JVHK597,并具有Leu营养缺陷、Ile营养缺陷、Met营养缺陷、α-AB抗性、2-TA抗性5种遗传标记.在未优化的条件下,菌株JVHK597摇瓶发酵72 h的产酸量达41.2 g/L.8次传代试验结果表明,菌株JVHK597的产酸能力稳定,经鉴定,菌株JVHK597的基因型为(Leu-,Ile-,Met-,α-ABr,2 -TAr),遗传标记具有稳定性.发酵培养基中硫酸镁( MgSO4·7H2O)和磷酸二氢钾的含量分别为0.6和1.4 g/L时,最有利于菌株生产L-缬氨酸.[结论]试验筛选出了L-缬氨酸高产菌株JVHK597,并为其发酵培养提供了指导.%[Objective]The aim was to screen superior strain of L-valine and study its fermentation condition. [ Method] With the mutant strain ZGH6128 of Brebvibacterium flavum as initial strain, 3 kinds of mutagens of ultraviolet (UV), diethyl sulfate (DES) and nitrosoguani-dine (NTG) were used in its mutagene treatments, its superior mutant strain of L-valine was screened out through shaking culture. [ Result] The strain ZGH6128 was treated with 3 kinds of mutagens of UV, DES and NTG and the mutant strain JVHK597 was obtained progressively. This mutant strain possessed 5 genetic marks of Leu auxotroph, Ile auxotroph, Met auxotroph, a-AB resistance and 2-TA resistance. Under non-optimized condition, the production of acid from the strain JVHK597 reached 41.2 g/L after fermentation for 72 h. The experimental results of 8 passages showed that the acid producing ability of the strain JVHK597 was stable and its genotype was identified to be (Leu-, Ile-, Met-, α-AB', 2-TA') and its genetic marks had stability. When the contents of bitter salt (Mg

  18. Abundance, source, and mode of occurrence of the inorganic constituents in coal

    Energy Technology Data Exchange (ETDEWEB)

    Finkelman, R. [US Geological Survey, Reston, VA (United States)

    1994-12-31

    The inorganic constituents, minerals and organically bound inorganic elements are commonly minor components of coal. Nevertheless, they can exert a significant influence on the economic value, utilization, and environmental impact of the coal. Some of the more common ways in which the inorganic constituents influence coal utilization are listed. Inorganic constituents affect virtually every aspect of coal utilization, from prospecting and mining to the disposal of cleaning and combustion wastes. In this chapter the more important inorganic constituents in coal are identified and their sources, distribution, modes of occurrence, and significance discussed. 60 refs., 4 tabs.

  19. Cooperative expression of atomic chirality in inorganic nanostructures

    Science.gov (United States)

    Wang, Peng-Peng; Yu, Shang-Jie; Govorov, Alexander O.; Ouyang, Min

    2017-02-01

    Cooperative chirality phenomena extensively exist in biomolecular and organic systems via intra- and inter-molecular interactions, but study of inorganic materials has been lacking. Here we report, experimentally and theoretically, cooperative chirality in colloidal cinnabar mercury sulfide nanocrystals that originates from chirality interplay between the crystallographic lattice and geometric morphology at different length scales. A two-step synthetic scheme is developed to allow control of critical parameters of these two types of handedness, resulting in different chiral interplays expressed as observables through materials engineering. Furthermore, we adopt an electromagnetic model with the finite element method to elucidate cooperative chirality in inorganic systems, showing excellent agreement with experimental results. Our study enables an emerging class of nanostructures with tailored cooperative chirality that is vital for fundamental understanding of nanoscale chirality as well as technology applications based on new chiroptical building blocks.

  20. A novel lattice energy calculation technique for simple inorganic crystals

    Science.gov (United States)

    Kaya, Cemal; Kaya, Savaş; Banerjee, Priyabrata

    2017-01-01

    In this pure theoretical study, a hitherto unexplored equation based on Shannon radii of the ions forming that crystal and chemical hardness of any crystal to calculate the lattice energies of simple inorganic ionic crystals has been presented. To prove the credibility of this equation, the results of the equation have been compared with experimental outcome obtained from Born-Fajans-Haber- cycle which is fundamentally enthalpy-based thermochemical cycle and prevalent theoretical approaches proposed for the calculation of lattice energies of ionic compounds. The results obtained and the comparisons made have demonstrated that the new equation is more useful compared to other theoretical approaches and allows to exceptionally accurate calculation of lattice energies of inorganic ionic crystals without doing any complex calculations.

  1. Survey of electrochemical production of inorganic compounds. Final report

    Energy Technology Data Exchange (ETDEWEB)

    1980-10-01

    The electrochemical generation of inorganic compounds, excluding chlorine/caustic, has been critically reviewed. About 60 x 10/sup 12/ Btu/y fossil fuel equivalent will be used in the year 2000 for the electrosynthesis of inorganic compounds. Significant energy savings in chlorate production can result from the development of suitable electrocatalysts for lowering the cathodic overpotential. Perchlorates, electrolytic hypochlorite, electrolytic manganese dioxide, fluorine and other miscellaneous compounds use relatively small amounts of electrical energy. Implementation of caustic scrubber technology for stack gas cleanup would result in appreciable amounts of sodium sulfate which could be electrolyzed to regenerate caustic. Hydrogen peroxide, now produced by the alkyl anthraquinone process, could be made electrolytically by a new process coupling anodic oxidation of sulfate with cathodic reduction of oxygen in alkaline solution. Ozone is currently manufactured using energy-inefficient silent discharge equipment. A novel energy-efficient approach which uses an oxygen-enhanced anodic reaction is examined.

  2. Biopolymer colloids for controlling and templating inorganic synthesis

    Directory of Open Access Journals (Sweden)

    Laura C. Preiss

    2014-11-01

    Full Text Available Biopolymers and biopolymer colloids can act as controlling agents and templates not only in many processes in nature, but also in a wide range of synthetic approaches. Inorganic materials can be either synthesized ex situ and later incorporated into a biopolymer structuring matrix or grown in situ in the presence of biopolymers. In this review, we focus mainly on the latter case and distinguish between the following possibilities: (i biopolymers as controlling agents of nucleation and growth of inorganic materials; (ii biopolymers as supports, either as molecular supports or as carrier particles acting as cores of core–shell structures; and (iii so-called “soft templates”, which include on one hand stabilized droplets, micelles, and vesicles, and on the other hand continuous scaffolds generated by gelling biopolymers.

  3. Gas Permeation Characteristics across Nano-Porous Inorganic Membranes

    Directory of Open Access Journals (Sweden)

    M.R Othman, H. Mukhtar

    2012-10-01

    Full Text Available An overview of parameters affecting gas permeation in inorganic membranes is presented. These factors include membrane physical characteristics, operational parameters and gas molecular characteristics. The membrane physical characteristics include membrane materials and surface area, porosity, pore size and pore size distribution and membrane morphology. The operational parameters include feed flow rate and concentration, stage cut, temperature and pressure. The gas molecular characteristics include gas molecular weight, diameter, critical temperature, critical pressure, Lennard-Jones parameters and diffusion volumes. The current techniques of material characterization may require complementary method in describing microscopic heterogeneity of the porous ceramic media. The method to be incorporated in the future will be to apply a stochastic model and/or fractal dimension. Keywords: Inorganic membrane, surface adsorption, Knudsen diffusion, Micro-porous membrane, permeation, gas separation.

  4. Mixtures of organic and inorganic substrates, particle size and proportion.

    Directory of Open Access Journals (Sweden)

    Emilio Raymundo Morales-Maldonado

    2015-06-01

    Full Text Available The objective of this paper was to review the mixtures of organic and inorganic materials used in the preparation of a new material, particle size, proportion, and their response in plant. In Mexico, agricultural waste is considered as a pollutant reservoir; however, from another perspective, this represents an industry with great potential. The nutrients ingested by animals represent nutriments available for plants when properly recycled. An option that minimizes the risk of contamination and improves its quality is the production of compost and vermicompost. Both processes are an alternative to organic production. A material by itself does not meet the optimum conditions. Reducing the volume of an organic material increases compaction and compression of roots, affecting the efficiency of irrigation and fertilization, so it is necessary to make mixtures with inorganic materials, that is used in the development of a new material for better growing conditions of the plant.

  5. Screening Method of New Inorganic Scintillators for Photon Counting

    Science.gov (United States)

    Pritchard, Megan

    2004-10-01

    Inorganic scintillators play an important role in detection and visualization of ionizing radiation. A scintillator with both high light yield and fast response has yet to be found. These methods are useful in detector applications for homeland security and nuclear non-proliferation. New scintillators are necessary to improve radiation detectors for detection of fissile materials specifically when shielded. At ORNL, several new inorganic scintillators including various versions of ZnO, and SnO2 are being evaluated to determine light yield and decay times. Crystals are grown here, doped or painted with metals such as Al, Cd, Sn or Ga and measured. The photons emitted from a scintillator from a single incident alpha or neutron can be counted and graphed, allowing the luminosity and decay constants to be determined. The promising samples are also being evaluated for exact luminosity through spectroscopy.

  6. Screening Method of Inorganic Scintillators for Photon Counting

    Science.gov (United States)

    Pritchard, M.

    2004-10-01

    Inorganic scintillators play an important role in detection and visualization of ionizing radiation. A scintillator with both high light yield and fast response has yet to be found. These methods are useful in detector applications for homeland security and nuclear non-proliferation. New scintillators are necessary to improve radiation detectors for detection of fissile materials specifically when shielded. At ORNL, several new inorganic scintillators including various versions of ZnO, and SnO2 are being evaluated to determine light yield and decay times. Crystals are grown here, doped or painted with metals such as Al, Cd, Sn or Ga and measured. The photons emitted from a scintillator from a single incident alpha or neutron can be counted and graphed, allowing the luminosity and decay constants to be determined

  7. Theory of hydrogen migration in organic-inorganic halide perovskites.

    Science.gov (United States)

    Egger, David A; Kronik, Leeor; Rappe, Andrew M

    2015-10-12

    Solar cells based on organic-inorganic halide perovskites have recently been proven to be remarkably efficient. However, they exhibit hysteresis in their current-voltage curves, and their stability in the presence of water is problematic. Both issues are possibly related to a diffusion of defects in the perovskite material. By using first-principles calculations based on density functional theory, we study the properties of an important defect in hybrid perovskites-interstitial hydrogen. We show that differently charged defects occupy different crystal sites, which may allow for ionization-enhanced defect migration following the Bourgoin-Corbett mechanism. Our analysis highlights the structural flexibility of organic-inorganic perovskites: successive iodide displacements, combined with hydrogen bonding, enable proton diffusion with low migration barriers. These findings indicate that hydrogen defects can be mobile and thus highly relevant for the performance of perovskite solar cells.

  8. Purificantion and characterization of inorganic pyrophosphatase from Thiobacillus thiooxidans.

    Science.gov (United States)

    Tominaga, N; Mori, T

    1977-02-01

    An inorganic pyrophosphatase [EC 3.6.1.1] was isolated from Thiobacillus thiooxidans and purified 975-fold to a state of apparent homogeneity. The enzyme catalyzed the hydrolysis of inorganic pyrophosphate and no activity was found with a variety of other phosphate esters. The cation Mg2+ was required for maximum activity; Co2+ and Mn2+ supported 25 per cent and 10.6 per cent of the activity with Mg2+, respectively. The pH optimum was 8.8. The molecular weight was estimated to be 88,000 by gel filtration and SDS gel electrophoresis, and the enzyme consisted of four identical subunits. The isoelectric point was found to be 5.05. The enzyme was exceptionally heat-stable in the presence of 0.01 M Mg2+.

  9. Determination of inorganic phosphate by electroanalytical methods: a review.

    Science.gov (United States)

    Berchmans, Sheela; Issa, Touma B; Singh, Pritam

    2012-06-01

    Determination of inorganic phosphate is of very high importance in environmental and health care applications. Hence knowledge of suitable analytical techniques available for phosphate sensing for different applications becomes essential. Electrochemical methods for determining inorganic phosphate have several advantages over other common techniques, including detection selectivity, stability and relative environmental insensitivity of electroactive labels. The different electrochemical sensing strategies adopted for the determination of phosphate using selective ionophores are discussed in this review. The various sensing strategies are classified based on the electrochemical detection techniques used viz., potentiometry, voltammetry, amperometry, unconventional electrochemical methods etc., The enzymatic sensing of phosphate coupled with electrochemical detection is also included. Various electroanalytical methods available in the literature are assessed for their merits in terms of selectivity, simplicity, miniaturisation, adaptability and suitability for field measurements.

  10. Stochastic modelling of dissolved inorganic nitrogen in space and time

    DEFF Research Database (Denmark)

    Lophaven, Søren Nymand; Carstensen, Niels Jacob; Rootzen, Helle

    2006-01-01

    Environmental monitoring datasets often contain a large amount of missing values, and are characterized as being sampled over time on a distinct number of locations in the area of interest. This paper proposes a stochastic approach for modelling such data in space and time, by taking the spatial...... and temporal correlations in data into account. It has been applied to observations of dissolved inorganic nitrogen in the Kattegat during the period 1993-1997. Modelling results are shown as maps of the spatial distribution of dissolved inorganic nitrogen (DIN) in 4 weeks, representing the four seasons......, and as time series of DIN at three different locations. However, the model approach could be applied to any space-time point given by a location in the Kattegat area and a week in the 5-year period 1993-1997. The results can be interpreted from a biological and physical point of view. Thus for the specific...

  11. Mixture interlayer for high performance organic-inorganic perovskite photodetectors

    Science.gov (United States)

    Tang, Feng; Chen, Qi; Chen, Lei; Ye, Fengye; Cai, Jinhua; Chen, Liwei

    2016-09-01

    Organic-inorganic perovskites are promising light absorbing active materials for photodetectors; however, the performance of current organic-inorganic perovskite-based photodetectors are limited by the high dark current due to hole injection at the cathode interlayer typically composed of fullerene derivatives. We have developed a mixture interlayer by simply blending polymethyl methacrylate (PMMA) with [6,6]-phenyl-C61-butyric acidmethyl ester (PCBM). Scanning Kelvin probe microscopy imaging reveals that the presence of PMMA reduced the work function of the PCBM:PMMA interlayer, which leads to increased energy barrier for hole injection and better hole-blocking property. Optimized perovskite photodetector with PCBM:PMMA hole-blocking interlayer exhibits a high detectivity of 1.1 × 1013 Jones, a broad linear dynamic range of 112 dB, and a fast response time of 2.2 μs.

  12. Organic-inorganic hybrid materials processing and applications

    OpenAIRE

    Schmidt, Helmut K.; Mennig, Martin; Nonninger, Ralph; Oliveira, Peter William de; Schirra, Hermann

    1999-01-01

    Hybrid materials as inorganic-organic nanostructured composites require tailored surface chemistry in order to obtain a homogeneous distribution of the nanoparticles in the matrix. For this reason, nanoparticles with organic functions have been synthesized, first, to provide the desired æ-potential at a given pH value, second, to avoid irreversible agglomeration due to the spacing effect, and third, to provide the appropriate surface chemistry. I could be shown that using this approach, it is...

  13. CONFINING CONDUCTING POLYANILINE IN A STABLE INORGANIC NETWORK

    Institute of Scientific and Technical Information of China (English)

    Yan-ju Wang; Nian-jiang Liu; Jin-long Lu; Jian Liu; Ji Li; Xia-bin Jing; Fo-song Wang; Xian-hong Wang

    2003-01-01

    Water soluble conducting polyaniline with electrical conductivity of 10-1-10-2 S/cm was prepared employing dopant induced water solubility technology. The water resistance of the conducting film was significantly improved employing sol-gel hybrids method, especially when the conductive polyaniline loading was below 30 wt%. The reason for the improvement is that the conducting polyaniline chains are confined in a stable inorganic network.

  14. Inorganic scintillators—a basic material for instrumentation in physics

    Science.gov (United States)

    Novotny, Rainer

    2005-01-01

    Since more than 100 years inorganic scintillators provide an efficient signal for photon and particle detection up to the highest energies. The paper provides a short review on the application of the most common scintillator materials used in nuclear and high-energy physics. Based on the general requirements for energy and momentum measurement, as well as particle identification, typical examples of detector concepts and operated systems are presented.

  15. Inorganic nanostructured materials for high performance electrochemical supercapacitors.

    Science.gov (United States)

    Liu, Sheng; Sun, Shouheng; You, Xiao-Zeng

    2014-02-21

    Electrochemical supercapacitors (ES) are a well-known energy storage system that has high power density, long life-cycle and fast charge-discharge kinetics. Nanostructured materials are a new generation of electrode materials with large surface area and short transport/diffusion path for ions and electrons to achieve high specific capacitance in ES. This mini review highlights recent developments of inorganic nanostructure materials, including carbon nanomaterials, metal oxide nanoparticles, and metal oxide nanowires/nanotubes, for high performance ES applications.

  16. Strongly coupled inorganic/nanocarbon hybrid materials for advanced electrocatalysis.

    Science.gov (United States)

    Liang, Yongye; Li, Yanguang; Wang, Hailiang; Dai, Hongjie

    2013-02-13

    Electrochemical systems, such as fuel cell and water splitting devices, represent some of the most efficient and environmentally friendly technologies for energy conversion and storage. Electrocatalysts play key roles in the chemical processes but often limit the performance of the entire systems due to insufficient activity, lifetime, or high cost. It has been a long-standing challenge to develop efficient and durable electrocatalysts at low cost. In this Perspective, we present our recent efforts in developing strongly coupled inorganic/nanocarbon hybrid materials to improve the electrocatalytic activities and stability of inorganic metal oxides, hydroxides, sulfides, and metal-nitrogen complexes. The hybrid materials are synthesized by direct nucleation, growth, and anchoring of inorganic nanomaterials on the functional groups of oxidized nanocarbon substrates including graphene and carbon nanotubes. This approach affords strong chemical attachment and electrical coupling between the electrocatalytic nanoparticles and nanocarbon, leading to nonprecious metal-based electrocatalysts with improved activity and durability for the oxygen reduction reaction for fuel cells and chlor-alkali catalysis, oxygen evolution reaction, and hydrogen evolution reaction. X-ray absorption near-edge structure and scanning transmission electron microscopy are employed to characterize the hybrids materials and reveal the coupling effects between inorganic nanomaterials and nanocarbon substrates. Z-contrast imaging and electron energy loss spectroscopy at single atom level are performed to investigate the nature of catalytic sites on ultrathin graphene sheets. Nanocarbon-based hybrid materials may present new opportunities for the development of electrocatalysts meeting the requirements of activity, durability, and cost for large-scale electrochemical applications.

  17. Gas Permeation Properties of Organic-inorganic Ultrathin Membranes

    Institute of Scientific and Technical Information of China (English)

    H. Kawakami

    2005-01-01

    @@ 1Introduction Recently, a great interest has been noted in the synthesis of inorganic membranes for gas separation. One of the candidates is a carbon molecular sieve (CMS) membrane, which is synthesized by the pyrolysis of a polymer. However, CMS membranes are very brittle and fragile. Additionally, it requires more careful handling and it is very difficult to prepare a thin CMS membrane because of its poor mechanical property. Therefore, the gas permeances of CMS membranes were not very high.

  18. Planar organic-inorganic hybrid perovskite solar cell by electrospray

    OpenAIRE

    Chen, Wenjun

    2015-01-01

    Recently, the organic-inorganic perovskite solar cell has attracted great attention due to the easy processing and rapid developed power conversion efficiency. The tri-halide perovskite CH3NH3PbI3-xClx possessing excellent optical and electronic properties, such as absorption hands span the visible region, long charge carrier diffusion lengths, and appropriate direct band gap, makes them ideal active layer material for photovoltaic devices. In this thesis, electrohydrodynamic spraying is used...

  19. Spontaneous Aerosol Ejection: Origin of Inorganic Particles in Biomass Pyrolysis.

    Science.gov (United States)

    Teixeira, Andrew R; Gantt, Rachel; Joseph, Kristeen E; Maduskar, Saurabh; Paulsen, Alex D; Krumm, Christoph; Zhu, Cheng; Dauenhauer, Paul J

    2016-06-08

    At high thermal flux and temperatures of approximately 500 °C, lignocellulosic biomass transforms to a reactive liquid intermediate before evaporating to condensable bio-oil for downstream upgrading to renewable fuels and chemicals. However, the existence of a fraction of nonvolatile compounds in condensed bio-oil diminishes the product quality and, in the case of inorganic materials, catalyzes undesirable aging reactions within bio-oil. In this study, ablative pyrolysis of crystalline cellulose was evaluated, with and without doped calcium, for the generation of inorganic-transporting aerosols by reactive boiling ejection from liquid intermediate cellulose. Aerosols were characterized by laser diffraction light scattering, inductively coupled plasma spectroscopy, and high-speed photography. Pyrolysis product fractionation revealed that approximately 3 % of the initial feed (both organic and inorganic) was transported to the gas phase as aerosols. Large bubble-to-aerosol size ratios and visualization of significant late-time ejections in the pyrolyzing cellulose suggest the formation of film bubbles in addition to the previously discovered jet formation mechanism.

  20. Inorganic and organic trace mineral supplementation in weanling pig diets.

    Science.gov (United States)

    Thomaz, Maria C; Watanabe, Pedro H; Pascoal, Leonardo A F; Assis, Murilo M; Ruiz, Urbano S; Amorim, Alessandro B; Silva, Susana Z; Almeida, Vivian V; Melo, Gabriel M P; Robles-Huaynate, Rizal A

    2015-01-01

    A study was conducted to evaluate the effects of dietary inorganic and organic trace minerals in two levels of supplementation regarding performance, diarrhea occurrence, hematological parameters, fecal mineral excretion and mineral retention in metacarpals and liver of weanling pigs. Seventy piglets weaned at 21 days of age with an average initial body weight of 6.70 ± 0.38 kg were allotted in five treatments: control diet (no added trace mineral premix); 50% ITMP (control diet with inorganic trace mineral premix supplying only 50% of trace mineral requirements); 50% OTMP (control diet with organic trace mineral premix supplying only 50% of trace mineral requirements); 100% ITMP (control diet with inorganic trace mineral premix supplying 100% of trace mineral requirements); and 100% OTMP (control diet with organic trace mineral premix supplying 100% of trace mineral requirements). Feed intake and daily weight gain were not affected by treatments, however, piglets supplemented by trace minerals presented better gain:feed ratio. No differences were observed at calcium, phosphorus, potassium, magnesium, sodium and sulfur excreted in feces per kilogram of feed intake. Treatments did not affect calcium, phosphorus, magnesium, sulfur and iron content in metacarpals. Trace mineral supplementation, regardless of level and source, improved the performance of piglets.

  1. Evaluation of Reclamability of Molding Sands with New Inorganic Binders

    Directory of Open Access Journals (Sweden)

    I. Izdebska-Szanda

    2012-04-01

    Full Text Available One of the purposes of the application of chemically modified inorganic binders is to improve knocking out properties and the related reclamability with previously used in foundry inorganic binder (water glass, which allowing the use of ecological binders for casting non- ferrous metals. Good knocking out properties of the sands is directly related to the waste sands reclamability, which is a necessary condition of effective waste management. Reclamation of moulding and core sands is a fundamental and effective way to manage waste on site at the foundry, in accordance with the Environmental Guidelines. Therefore, studies of reclamation of waste moulding and core sands with new types of inorganic binders (developed within the framework of the project were carried out. These studies allowed to determine the degree of recovery of useful, material, what the reclaimed sand is, and the degree of its use in the production process. The article presents these results of investigation. They are a part of broader research programme executed under the project POIG.01.01.02-00- 015/09 "Advanced materials and technologies".

  2. Study of nonproportionality in the light yield of inorganic scintillators

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Jai [School of Engineering and IT, B-purple-12, Faculty of EHSE, Charles Darwin University, Darwin, Northern Territory 0909 (Australia)

    2011-07-15

    Using a phenomenological approach, the light yield is derived for inorganic scintillators as a function of the rates of linear, bimolecular, and Auger processes occurring in the electron track initiated by an x ray or a {gamma}-ray photon. A relation between the track length and incident energy is also derived. It is found that the nonproportionality in the light yield can be eliminated if either nonlinear processes of interaction among the excited electrons, holes, and excitons can be eliminated from occurring or the high density situation can be relieved by diffusion of carriers from the track at a faster rate than the rate of activation of nonlinear processes. The influence of the track length and radius on the yield nonproportionality is discussed in view of the known experimental results. Inventing new inorganic scintillating materials with high carrier mobility can lead to a class of proportional inorganic scintillators. Results agree qualitatively with experimental results for the dependence of light yield on the incident energy.

  3. Nanoporous ultra-high specific surface inorganic fibres

    Science.gov (United States)

    Kanehata, Masaki; Ding, Bin; Shiratori, Seimei

    2007-08-01

    Nanoporous inorganic (silica) nanofibres with ultra-high specific surface have been fabricated by electrospinning the blend solutions of poly(vinyl alcohol) (PVA) and colloidal silica nanoparticles, followed by selective removal of the PVA component. The configurations of the composite and inorganic nanofibres were investigated by changing the average silica particle diameters and the concentrations of colloidal silica particles in polymer solutions. After the removal of PVA by calcination, the fibre shape of pure silica particle assembly was maintained. The nanoporous silica fibres were assembled as a porous membrane with a high surface roughness. From the results of Brunauer-Emmett-Teller (BET) measurements, the BET surface area of inorganic silica nanofibrous membranes was increased with the decrease of the particle diameters. The membrane composed of silica particles with diameters of 15 nm showed the largest BET surface area of 270.3 m2 g-1 and total pore volume of 0.66 cm3 g-1. The physical absorption of methylene blue dye molecules by nanoporous silica membranes was examined using UV-vis spectrometry. Additionally, the porous silica membranes modified with fluoroalkylsilane showed super-hydrophobicity due to their porous structures.

  4. Nanoporous ultra-high specific surface inorganic fibres

    Energy Technology Data Exchange (ETDEWEB)

    Kanehata, Masaki [Faculty of Science and Technology, Keio University, Yokohama 223-8522 (Japan); Ding Bin [Fiber and Polymer Science, University of California, Davis, CA 95616 (United States); Shiratori, Seimei [Faculty of Science and Technology, Keio University, Yokohama 223-8522 (Japan)

    2007-08-08

    Nanoporous inorganic (silica) nanofibres with ultra-high specific surface have been fabricated by electrospinning the blend solutions of poly(vinyl alcohol) (PVA) and colloidal silica nanoparticles, followed by selective removal of the PVA component. The configurations of the composite and inorganic nanofibres were investigated by changing the average silica particle diameters and the concentrations of colloidal silica particles in polymer solutions. After the removal of PVA by calcination, the fibre shape of pure silica particle assembly was maintained. The nanoporous silica fibres were assembled as a porous membrane with a high surface roughness. From the results of Brunauer-Emmett-Teller (BET) measurements, the BET surface area of inorganic silica nanofibrous membranes was increased with the decrease of the particle diameters. The membrane composed of silica particles with diameters of 15 nm showed the largest BET surface area of 270.3 m{sup 2} g{sup -1} and total pore volume of 0.66 cm{sup 3} g{sup -1}. The physical absorption of methylene blue dye molecules by nanoporous silica membranes was examined using UV-vis spectrometry. Additionally, the porous silica membranes modified with fluoroalkylsilane showed super-hydrophobicity due to their porous structures.

  5. Tuning physical properties by assembling subnanometer inorganic and organic units

    Science.gov (United States)

    Zhang, Yong; Parilla, P. A.; Ahrenkiel, S. P.; Mascarenhas, A.; Islam, Z.; Ren, Y.; Lee, P. L.; McNevin, M. J.; Naumov, I.; Fu, H. X.; Huang, X. Y.; Li, J.

    2008-03-01

    Designing inorganic-organic hybrid materials in a nanoscopic scale allows taking the full advantage of the two worlds, which has recently been demonstrated in a new family of hybrid crystalline materials that are the fully ordered assemblies of sub-nanometer scale inorganic units (e.g., few monolayer-thick slab, single atomic chain) and organic molecules[1].They have been shown to exhibit a number of unique properties that are not readily available in either of the components or their nanostructures: for instance, strongly enhanced exciton-polariton absorption and exciton binding energy[2], a massive bandgap blue shift (˜ 2 eV) from that of the bulk inorganic semiconductor[3], and fine-tuning of thermal expansion and achieving zero-thermal expansio[4]. They have great potential for applications in areas including transparent conducting materials, thermoelectric materials, UV optoelectronic devices, because of their unusual electronic, vibrational and optical properties and the flexibility in tailoring the material properties adapting to the specific application requirements. .[1] X. H. Huang et al., JACS 125, 7049 (03). [2] Y. Zhang et al., PRL 96, 26405 (06). [3] B. Fluegel et al., PRB 70, 205308 (04). [4] Y. Zhang et al., PRL 99, 215901 (07).

  6. Contrasting modes of inorganic carbon acquisition amongst Symbiodinium (Dinophyceae) phylotypes.

    Science.gov (United States)

    Brading, Patrick; Warner, Mark E; Smith, David J; Suggett, David J

    2013-10-01

    Growing concerns over ocean acidification have highlighted the need to critically understand inorganic carbon acquisition and utilization in marine microalgae. Here, we contrast these characteristics for the first time between two genetically distinct dinoflagellate species of the genus Symbiodinium (phylotypes A13 and A20) that live in symbiosis with reef-forming corals. Both phylotypes were grown in continuous cultures under identical environmental conditions. Rubisco was measured using quantitative Western blots, and radioisotopic (14) C uptake was used to characterize light- and total carbon dioxide (TCO2 )-dependent carbon fixation, as well as inorganic carbon species preference and external carbonic anhydrase activity. A13 and A20 exhibited similar rates of carbon fixation despite cellular concentrations of Rubisco being approximately four-fold greater in A13. The uptake of CO2 over HCO3 - was found to support the majority of carbon fixation in both phylotypes. However, A20 was also able to indirectly utilize HCO3 - by first converting it to CO2 via external carbonic anhydrase. These results show that adaptive differences in inorganic carbon acquisition have evolved within the Symbiodinium genus, which thus carries fundamental implications as to how this functionally key genus will respond to ocean acidification, but could also represent a key trait factor that influences their productivity when in hospite of their coral hosts.

  7. Inorganic arsenic exposure and type 2 diabetes mellitus in Mexico.

    Science.gov (United States)

    Coronado-González, José Antonio; Del Razo, Luz María; García-Vargas, Gonzalo; Sanmiguel-Salazar, Francisca; Escobedo-de la Peña, Jorge

    2007-07-01

    Inorganic arsenic exposure in drinking water has been recently related to diabetes mellitus. To evaluate this relationship the authors conducted in 2003, a case-control study in an arseniasis-endemic region from Coahuila, a northern state of Mexico with a high incidence of diabetes. The present analysis includes 200 cases and 200 controls. Cases were obtained from a previous cross-sectional study conducted in that region. Diagnosis of diabetes was established following the American Diabetes Association criteria, with two fasting glucose values > or = 126 mg/100 ml (> or = 7.0 mmol/l) or a history of diabetes treated with insulin or oral hypoglycemic agents. The next subject studied, subsequent to the identification of a case in the cross-sectional study was taken as control. Inorganic arsenic exposure was measured through total arsenic concentrations in urine, measured by hydride-generation atomic absorption spectrophotometry. Subjects with intermediate total arsenic concentration in urine (63.5-104 microg/g creatinine) had two-fold higher risk of having diabetes (odds ratio=2.16; 95% confidence interval: 1.23, 3.79), but the risk was almost three times greater in subjects with higher concentrations of total arsenic in urine (odds ratio=2.84; 95% confidence interval: 1.64, 4.92). This data provides additional evidence that inorganic arsenic exposure may be diabetogenic.

  8. Relation of organic and inorganic substances in formation of urolyths

    Directory of Open Access Journals (Sweden)

    A. K. Poliyenko

    2012-01-01

    Full Text Available Macro- and microscopic structural features of human urolyths have been studied to reveal the relation between organic and inorganic components and the role of the latter in the process of urolyth formation and growth. The combined study of the shape, color, surface, mineral and organic composition, and internal structure and zoning of 788 urolyths has been performed. Crystallomorphological, polarization-optical, X-ray-diffraction, electron-microscopic, chemical, neutron-activation, and computer technologies of study of the urolyth structure have been used. It has been found that macroscopic characteristics of uroluths (color, shape, surface, and size did not reflect the chemical composition of urolyths. In the structure of abundance of urolyths in Tomskand the Tomsk Region, oxalates (58% and urolyths of complex mineral composition (29%  prevail. It has been found that an urolyth is an organomineral aggregate having the internal structure formed by a rhythm of alternation of organic and inorganic layers and the character of arrangement of individual mineral crystals, and the internal structure is independent of the chemical composition of the urolyth and  uniform in urolyths of different chemical composition. The most part of urolyths has a mixed (44% or druzy (35% type of crystal arrangement and the  combined (45% or grainy (31% rhythm of alternation of organic and inorganic components.

  9. Contrasting impact of organic and inorganic nanoparticles and colloids on the behavior of particle-reactive elements in tropical estuaries: An experimental study

    Science.gov (United States)

    Merschel, Gila; Bau, Michael; Dantas, Elton Luiz

    2017-01-01

    Estuarine processes may affect the flux of dissolved organic carbon (DOC), iron and other particle-reactive elements such as the rare earth elements and yttrium (REY), into the ocean via salt-induced coagulation and subsequent removal of river-borne (nano-)particles and colloids. We experimentally assessed the impact of the admixture of seawater on DOC, Fe and REY associated with inorganic and organic nanoparticles and colloids (NPCs) present in tropical rivers, using Rio Solimões and Rio Negro, which are particularly rich in inorganic and organic NPCs, respectively, as river water endmembers. Similar to the conservative elements Sr, Rb and U, DOC behaves conservatively in all mixing experiments, whereas strong removal of Fe and REY (and preferential removal of light over heavy REY and of Ce relative to La and Pr) is confined to experiments with inorganic NPC-rich Rio Solimões water. This removal already occurs at very low salinity and is due to the aggregation of the inorganic NPCs. However, REY removal efficiency increases gradually with increasing salinity, which is in marked contrast to DOC-poor Arctic river waters from which REY removal at lowest salinity is significantly stronger. This suggests that the DOC concentrations in the water have a profound impact on the estuarine mixing behavior of particle-reactive elements. In marked contrast to the Rio Solimões mixing experiment, Fe and the REY in experiments with Rio Negro water behave similarly to DOC and mix conservatively with seawater, indicating that the organic NPCs, most of which are humic and fulvic acids, and their associated trace elements are much less susceptible to coagulation and estuarine removal than inorganic ones. Even at higher salinities, estuarine REY removal from inorganic NPC-rich Rio Solimões water significantly exceeds REY removal from organic NPC-rich Rio Negro water. Hence, the combination of higher element concentrations in and of less estuarine removal from organic NPC

  10. Comparison of selenium distribution in mice organs after the supplementation with inorganic and organic selenium compound selenosemicarbazide.

    Science.gov (United States)

    Musik, Irena; Kozioł-Montewka, Maria; Toś-Luty, Sabina; Donica, Helena; Pasternak, Kazimierz; Wawrzycki, Sławomir

    2002-01-01

    Studies on selenium organ content and its function in living organisms just like studies on other elements provide interesting results although their interpretation is not always clear. The aim of our study was to determine the concentration and distribution of selenium in several organs and tissues in mice after supplementation with our newly synthesized organic compound of selenium selenosemicarbazide (4-o-tolyl-selenosemicarbazide of o-chlorobenzoic acid) as compared to the effects of the supplementation with inorganic compounds. SWISS mice were fed with both types of compounds at the dose of 10(-3) g Se per kg for the period of 10 days. The concentrations of selenium in brains of mice treated with selenocarbazide and sodium selenite were higher than in controls (38.04 micrograms g-1 and 32.00 micrograms g-1 vs. 26.18 micrograms g-1). There was a statistically significant increase in the selenium contents in lungs after supplementation with selenosemicarbazide and sodium selenite (11.81 micrograms g-1 and 6.79 micrograms g-1 vs. 1.75 micrograms g-1 in controls). We found a statistically insignificant increase in selenium contents in intercostal muscles after supplementation with inorganic selenium compounds and a statistically significant increase after the supplementation with selenosemicarbazide (10.13 micrograms g-1; 14.21 micrograms g-1 and 28.84 micrograms g-1, respectively). Our investigations lead to a conclusion that 4-o-tolyl-seleno-semicarbazide of o-chlorobenzoic acid, an organic selenium compound may be more easily absorbed than inorganic sodium IV selenite.

  11. Synthesis, Processing, and Characterization of Inorganic-Organic Hybrid Cross-Linked Silica, Organic Polyimide, and Inorganic Aluminosilicate Aerogels

    Science.gov (United States)

    Nguyen, Baochau N.; Guo, Haiquan N.; McCorkle, Linda S.

    2014-01-01

    As aerospace applications become ever more demanding, novel insulation materials with lower thermal conductivity, lighter weight and higher use temperature are required to fit the aerospace application needs. Having nanopores and high porosity, aerogels are superior thermal insulators, among other things. The use of silica aerogels in general is quite restricted due to their inherent fragility, hygroscopic nature, and poor mechanical properties, especially in extereme aerospace environments. Our research goal is to develop aerogels with better mechanical and environmental stability for a variety of aeronautic and space applications including space suit insulation for planetary surface missions, insulation for inflatable structures for habitats, inflatable aerodynamic decelerators for entry, descent and landing (EDL) operations, and cryotank insulation for advance space propulsion systems. Different type of aerogels including organic-inorganic polymer reinforced (hybrid) silica-based aerogels, polyimide aerogels and inorganic aluminosilicate aerogels have been developed and examined.

  12. Dimethylarsinic acid in drinking water changed the morphology but not the expression of DNA repair genes of bladder transitional epithelium in F344 rats

    Science.gov (United States)

    Inorganic arsenic increases urinary bladder transitional cell carcinoma in humans. In laboratory animals, it is dimethylarsinic acid [DMA(V)], a major arsenic metabolite in the urine of inorganic arsenic-exposed people, that increases transitional cell carcinoma, namely in F344 r...

  13. Inorganic bromine in the marine boundary layer: a critical review

    Directory of Open Access Journals (Sweden)

    R. Sander

    2003-06-01

    Full Text Available The cycling of inorganic bromine in the marine boundary layer (mbl has received increased attention in recent years. Bromide, a constituent of sea water, is injected into the atmosphere in association with sea-salt aerosol by breaking waves on the ocean surface. Measurements reveal that supermicrometer sea-salt aerosol is depleted in bromine by about 50% relative to conservative tracers, whereas marine submicrometer aerosol is often enriched in bromine. Model calculations, laboratory studies, and field observations strongly suggest that these depletions reflect the chemical transformation of particulate bromide to reactive inorganic gases that influence the processing of ozone and other important constituents of marine air. However, currently available techniques cannot reliably quantify many chem{Br}-containing compounds at ambient concentrations and, consequently, our understanding of inorganic Br cycling over the oceans and its global significance are uncertain. To provide a more coherent framework for future research, we have reviewed measurements in marine aerosol, the gas phase, and in rain. We also summarize sources and sinks, as well as model and laboratory studies of chemical transformations. The focus is on inorganic bromine over the open oceans, excluding the polar regions. The generation of sea-salt aerosol at the ocean surface is the major tropospheric source producing about 6.2 Tg/a of bromide. The transport of  Br from continents (as mineral aerosol, and as products from biomass-burning and fossil-fuel combustion can be of local importance. Transport of degradation products of long-lived Br-containing compounds from the stratosphere and other sources contribute lesser amounts. Available evidence suggests that, following aerosol acidification, sea-salt bromide reacts to form Br2 and BrCl that volatilize to the gas phase and photolyze in daylight to produce atomic Br and Cl. Subsequent transformations can destroy

  14. Organic/Inorganic Hybrid Nanostructures for Chemical Plasmonic Sensors

    Science.gov (United States)

    Chang, Sehoon

    2011-12-01

    The work presented in this dissertation suggests novel design of chemical plasmonic sensors which have been developed based on Localized Surface Plasmon Resonance (LSPR), and Surface-enhanced Raman scattering (SERS) phenomena. The goal of the study is to understand the SERS phenomena for 3D hybrid (organic/inorganic) templates and to design of the templates for trace-level detection of selected chemical analytes relevant to liquid explosives and hazardous chemicals. The key design criteria for the development of the SERS templates are utilizing selective polymeric nanocoatings within cylindrical nanopores for promoting selective adsorption of chemical analyte molecules, maximizing specific surface area, and optimizing concentration of hot spots with efficient light interaction inside nanochannels. The organic/inorganic hybrid templates are optimized through a comprehensive understanding of the LSPR properties of the gold nanoparticles, gold nanorods, interaction of light with highly porous alumina template, and the choice of physical and chemical attributes of the selective coating. Furthermore, novel method to assemble silver nanoparticles in 3D as the active SERS-active substrate has been demonstrated by uniform, in situ growth of silver nanoparticles from electroless deposited silver seeds excluding any adhesive polymer layer on template. This approach can be the optimal for SERS sensing applications because it is not necessary to separate the Raman bands of the polyelectrolyte binding layer from those of the desired analyte. The fabrication method is an efficient, simple and fast way to assemble nanoparticles into 3D nanostructures. Addressable Raman markers from silver nanowire crossbars with silver nanoparticles are also introduced and studied. Assembly of silver nanowire crossbar structure is achieved by simple, double-step capillary transfer lithography. The on/off SERS properties can be observed on silver nanowire crossbars with silver nanoparticles

  15. Aluminum corrosion mitigation in alkaline electrolytes containing hybrid inorganic/organic inhibitor system for power sources applications

    Science.gov (United States)

    Gelman, Danny; Lasman, Itay; Elfimchev, Sergey; Starosvetsky, David; Ein-Eli, Yair

    2015-07-01

    The severe corrosion accompanied with hydrogen evolution process is the main obstacle preventing the implementation of Al as an anode in alkaline batteries. It impairs the functionality of alkaline battery, due to a drastic capacity loss and a short shelf life. The possibility to reduce Al corrosion rate in alkaline solution with the use of hybrid organic∖inorganic inhibitor based on poly (ethylene glycol) di-acid (PEG di-acid) and zinc oxide (ZnO) was examined in this work. A correlation between an Al corrosion rates and the concentrations of both PEG di-acid and ZnO in alkaline is shown. Selecting 5000 ppm PEG di-acid and 16 gr/l ZnO provides substantial corrosion protection of Al, reducing the corrosion rate in a strong alkaline solution by more than one order of magnitude. Moreover, utilizing the same formulation results in increase in Al-air battery discharge capacity, from 44.5 (for a battery utilizing only KOH in the electrolyte) to 70 mhA/cm2 (for a battery utilizing ZnO/PEG di-acid hybrid inhibitor in the electrolyte). The morphology and composition of the Al electrode surface (studied by SEM, EDS, and XRD) depend on PEG di-acid and ZnO concentrations.

  16. Hyaluronic acid for anticancer drug and nucleic acid delivery.

    Science.gov (United States)

    Dosio, Franco; Arpicco, Silvia; Stella, Barbara; Fattal, Elias

    2016-02-01

    Hyaluronic acid (HA) is widely used in anticancer drug delivery, since it is biocompatible, biodegradable, non-toxic, and non-immunogenic; moreover, HA receptors are overexpressed on many tumor cells. Exploiting this ligand-receptor interaction, the use of HA is now a rapidly-growing platform for targeting CD44-overexpressing cells, to improve anticancer therapies. The rationale underlying approaches, chemical strategies, and recent advances in the use of HA to design drug carriers for delivering anticancer agents, are reviewed. Comprehensive descriptions are given of HA-based drug conjugates, particulate carriers (micelles, liposomes, nanoparticles, microparticles), inorganic nanostructures, and hydrogels, with particular emphasis on reports of preclinical/clinical results.

  17. Acid-base bifunctional catalytic surfaces for nucleophilic addition reactions.

    Science.gov (United States)

    Motokura, Ken; Tada, Mizuki; Iwasawa, Yasuhiro

    2008-09-01

    This article illustrates the modification of oxide surfaces with organic amine functional groups to create acid-base bifunctional catalysts, summarizing our previous reports and also presenting new data. Immobilization of organic amines as bases on inorganic solid-acid surfaces afforded highly active acid-base bifunctional catalysts, which enabled various organic transformations including C--C coupling reactions, though these reactions did not proceed with either the homogeneous amine precursors or the acidic supports alone. Spectroscopic characterization, such as by solid-state MAS NMR and FTIR, revealed not only the interactions between acidic and basic sites but also bifunctional catalytic reaction mechanisms.

  18. Recovery of carboxylic acids produced by fermentation.

    Science.gov (United States)

    López-Garzón, Camilo S; Straathof, Adrie J J

    2014-01-01

    Carboxylic acids such as citric, lactic, succinic and itaconic acids are useful products and are obtained on large scale by fermentation. This review describes the options for recovering these and other fermentative carboxylic acids. After cell removal, often a primary recovery step is performed, using liquid-liquid extraction, adsorption, precipitation or conventional electrodialysis. If the carboxylate is formed rather than the carboxylic acid, the recovery process involves a step for removing the cation of the formed carboxylate. Then, bipolar electrodialysis and thermal methods for salt splitting can prevent that waste inorganic salts are co-produced. Final carboxylic acid purification requires either distillation or crystallization, usually involving evaporation of water. Process steps can often be combined synergistically. In-situ removal of carboxylic acid by extraction during fermentation is the most popular approach. Recovery of the extractant can easily lead to waste inorganic salt formation, which counteracts the advantage of the in-situ removal. For industrial production, various recovery principles and configurations are used, because the fermentation conditions and physical properties of specific carboxylic acids differ.

  19. Survey of total and inorganic arsenic content in blue mussels (Mytilus edulis L.) from Norwegian fiords: Revelation of unusual high levels of inorganic arsenic

    DEFF Research Database (Denmark)

    Sloth, Jens Jørgen; Julshamn, Kåre

    2008-01-01

    The present study reports the findings of unusual high levels of inorganic arsenic in samples of blue mussels (Mytilus edulis L.). A total of 175 pooled samples of blue mussels from various locations along the Norwegian coastline were analyzed for their content of total arsenic and inorganic...

  20. The chemical composition of inorganic and carbonaceous materials in PM 2.5 in Nanjing, China

    Science.gov (United States)

    Yang, Hong; Yu, Jian Zhen; Ho, Steven Sai Hang; Xu, Jinhui; Wu, Wai-Shing; Wan, Chun Hong; Wang, Xiaodong; Wang, Xiaorong; Wang, Liansheng

    PM 2.5 samples were collected at an urban and a suburban site in Nanjing, China in 2001. They were analyzed for inorganic ions, elemental carbon, organic carbon (OC), water-soluble organic carbon (WSOC), and individual WSOC and nonpolar organic species. Sulfate and organic matter were the two most abundant constituents in these samples. Sulfate accounted for an average of 23% (urban site) and 30% (suburban site) of the identified aerosol mass. Organic matter accounted for an average of 37% (urban) and 28% (suburban) of the identified aerosol mass. WSOC was a significant portion of OC, accounting for about one-third of OC at the urban site and 45% of OC at the suburban site. The suburban-urban gradient in the WSOC/OC ratio also reflected that the aerosol OC was more aged at the suburban location. The correlations of WSOC with sulfate and nitrate suggest that the WSOC fraction was dominated by secondary organics. More than 30 individual WSOC species in the compound classes of organic anions, amino acids, aliphatic amines, and carbohydrates were quantified, accounting for approximately 8% of the WSOC on a carbon mass basis. In addition, 46 individual nonpolar organic compounds in the compound classes of n-alkanes, hopanes, and polycyclic aromatic hydrocarbons were quantified using an in-injection port thermal desorption technique. These nonpolar organic species accounted for less than 7% of the OC on a carbon mass basis. The quantification of individual compounds allowed the identification of major aerosol sources through principal component analysis. Coal combustion, vehicular emissions, secondary inorganic and organic aerosols, and road/sea salt were the major contributing sources to the identified PM 2.5 aerosol mass.

  1. Organic and inorganic composition and microbiology of produced waters from Pennsylvania shale gas wells

    Science.gov (United States)

    Akob, Denise M.; Cozzarelli, Isabelle M.; Dunlap, Darren S.; Rowan, Elisabeth L.; Lorah, Michelle M.

    2015-01-01

    Hydraulically fractured shales are becoming an increasingly important source of natural gas production in the United States. This process has been known to create up to 420 gallons of produced water (PW) per day, but the volume varies depending on the formation, and the characteristics of individual hydraulic fracture. PW from hydraulic fracturing of shales are comprised of injected fracturing fluids and natural formation waters in proportions that change over time. Across the state of Pennsylvania, shale gas production is booming; therefore, it is important to assess the variability in PW chemistry and microbiology across this geographical span. We quantified the inorganic and organic chemical composition and microbial communities in PW samples from 13 shale gas wells in north central Pennsylvania. Microbial abundance was generally low (66–9400 cells/mL). Non-volatile dissolved organic carbon (NVDOC) was high (7–31 mg/L) relative to typical shallow groundwater, and the presence of organic acid anions (e.g., acetate, formate, and pyruvate) indicated microbial activity. Volatile organic compounds (VOCs) were detected in four samples (∼1 to 11.7 μg/L): benzene and toluene in the Burket sample, toluene in two Marcellus samples, and tetrachloroethylene (PCE) in one Marcellus sample. VOCs can be either naturally occurring or from industrial activity, making the source of VOCs unclear. Despite the addition of biocides during hydraulic fracturing, H2S-producing, fermenting, and methanogenic bacteria were cultured from PW samples. The presence of culturable bacteria was not associated with salinity or location; although organic compound concentrations and time in production were correlated with microbial activity. Interestingly, we found that unlike the inorganic chemistry, PW organic chemistry and microbial viability were highly variable across the 13 wells sampled, which can have important implications for the reuse and handling of these fluids

  2. Inorganic Water Repellent Coatings for Thermal Protection Insulation on an Aerospace Vehicle

    Science.gov (United States)

    Fuerstenau, D. W.; Huang, P.; Ravikumar, R.

    1997-01-01

    The objective of this research was two-fold: first, to identify and test inorganic water-repellent materials that would be hydrophobic even after thermal cycling to temperatures above 600 C and, second, to develop a model that would link hydrophobicity of a material to the chemical properties of its constituent atoms. Four different materials were selected for detailed experimental study, namely, boron nitride, talc, molybdenite, and pyrophyllite, all of which have a layered structure made up of ionic/covalent bonds within the layers but with van der Waals bonds between the layers. The materials tested could be considered hydrophobic for a nonporous surface but none of the observed contact angles exceeded the necessary 90 degrees required for water repellency of porous materials. Boron nitride and talc were observed to retain their water-repellency when heated in air to temperatures that did not exceed 800 C, and molybdenite was found to be retain its hydrophobicity when heated to temperatures up to 600 C. For these three materials, oxidation and decomposition were identified to be the main cause for the breakdown of water repellency after repeated thermal cycling. Pyrophyllite shows the maximum promise as a potential water-repellent inorganic material, which, when treated initially at 900 C, retained its shape and remained hydrophobic for two thermal cycles where the maximum retreatment temperature is 900 C. A model was developed for predicting materials that might exhibit hydrophobicity by linking two chemical properties, namely, that the constituent ions of the compound belong to the soft acid-base category and that the fractional ionic character of the bonds be less than about 20 percent.

  3. Identification of inorganic improvised explosive devices using sequential injection capillary electrophoresis and contactless conductivity detection.

    Science.gov (United States)

    Blanco, Gustavo A; Nai, Yi H; Hilder, Emily F; Shellie, Robert A; Dicinoski, Greg W; Haddad, Paul R; Breadmore, Michael C

    2011-12-01

    A simple sequential injection capillary electrophoresis (SI-CE) instrument with capacitively coupled contactless conductivity detection (C(4)D) has been developed for the rapid separation of anions relevant to the identification of inorganic improvised explosive devices (IEDs). Four of the most common explosive tracer ions, nitrate, perchlorate, chlorate, and azide, and the most common background ions, chloride, sulfate, thiocyanate, fluoride, phosphate, and carbonate, were chosen for investigation. Using a separation electrolyte comprising 50 mM tris(hydroxymethyl)aminomethane, 50 mM cyclohexyl-2-aminoethanesulfonic acid, pH 8.9 and 0.05% poly(ethyleneimine) (PEI) in a hexadimethrine bromide (HDMB)-coated capillary it was possible to partially separate all 10 ions within 90 s. The combination of two cationic polymer additives (PEI and HDMB) was necessary to achieve adequate selectivity with a sufficiently stable electroosmotic flow (EOF), which was not possible with only one polymer. Careful optimization of variables affecting the speed of separation and injection timing allowed a further reduction of separation time to 55 s while maintaining adequate efficiency and resolution. Software control makes high sample throughput possible (60 samples/h), with very high repeatability of migration times [0.63-2.07% relative standard deviation (RSD) for 240 injections]. The separation speed does not compromise sensitivity, with limits of detection ranging from 23 to 50 μg·L(-1) for all the explosive residues considered, which is 10× lower than those achieved by indirect absorbance detection and 2× lower than those achieved by C(4)D using portable benchtop instrumentation. The combination of automation, high sample throughput, high confidence of peak identification, and low limits of detection makes this methodology ideal for the rapid identification of inorganic IED residues.

  4. Assimilation of organic and inorganic nutrients by Erica root fungi from the fynbos ecosystem.

    Science.gov (United States)

    Bizabani, Christine; Dames, Joanna Felicity

    2016-03-01

    Erica dominate the fynbos ecosystem, which is characterized by acidic soils that are rich in organic matter. The ericaceae associate with ericoid mycorrhizal (ERM) fungi for survival. In this study fungal biomass accumulation in vitro was used to determine nutrient utilisation of various inorganic and organic substrates. This is an initial step towards establishment of the ecological roles of typical ERM fungi and other root fungi associated with Erica plants, with regard to host nutrition. Meliniomyces sp., Acremonium implicatum, Leohumicola sp., Cryptosporiopsis erica, Oidiodendron maius and an unidentified Helotiales fungus were selected from fungi previously isolated and identified from Erica roots. Sole nitrogen sources ammonium, nitrate, arginine and Bovine Serum Albumin (BSA) were tested. Meliniomyces and Leohumicola species were able to utilise BSA effectively. Phosphorus nutrition was tested using orthophosphate, sodium inositol hexaphosphate and DNA. Most isolates preferred orthophosphate. Meliniomyces sp. and A. implicatum were able to accumulate significant biomass using DNA. Carbon utilisation was tested using glucose, cellobiose, carboxymethylcellulose, pectin and tannic acid substrates. All fungal isolates produced high biomass on glucose and cellobiose. The ability to utilize organic nutrient sources in culture, illustrates their potential role of these fungi in host nutrition in the fynbos ecosystem.

  5. Fabrication and characterization of materials and structures for hybrid organic-inorganic photonics

    Science.gov (United States)

    Haško, Daniel; Chovan, Jozef; Uherek, František

    2017-03-01

    Hybrid organic-inorganic integrated photonics integrate the organic material, as a part of active layer, with inorganic structure, and it is the organic component that extends the functionalities as compared to inorganic photonics. This paper presents the results of fabrication and characterization of inorganic and organic layers, as well as of hybrid organic-inorganic structures. Inorganic oxide and nitride materials and structures were grown using plasma enhanced chemical vapor deposition. As a substrate for tested organic layers and for preparation of multilayer structures, commercially available SiO2 created by thermal oxidation on Si was used. The hybrid organic-inorganic structures were prepared by spin coating of organic materials on SiO2/Si inorganic structures. As the basic photonics devices, the testing strip inorganic and organic waveguides were fabricated using reactive ion etching. The shape of fabricated testing waveguides was trapezoidal and etched structures were able to guide the radiation. The presented technology enabled to prepare hybrid organic-inorganic structures of comparable dimensions and shape. The fabricated waveguides dimensions and shape will be used for optimisation and design of new lithographic mask to prepare photonic components with required characteristics.

  6. Phenolic Acids in Plant-Soil-Microbe System: A Review

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Phenolic acids are very common compounds in pedosphere. The objective of this review was to summarize the current knowledge of the behaviors of phenolic acids in plant-soil-microbe system. When phenolic acids originated from leaching, decomposition and exudation of living and dead plant tissues enter soils, they can react physicochemically with soil particle surfaces and/or incorporate into humic matter. Phenolic acids desorbed from soil particle surfaces and remained in solution phase can be utilized by microbe as carbon sources and absorbed by plants. The degradation products of phenolic acids by microbe include some organic and/or inorganic compounds such as new phenolic acids. In addition, phenolic acids in soils can stimulate population and activity of microbe. Phenolic acids can inhibit plants growth by affecting ion leakage, phytohormone activity, membrane permeability, hydraulic conductivity, net nutrient uptake, and enzyme activity. Behaviors of phenolic acids in soils are influenced by other organic compounds (phenolic acids, methionine, glucose, etc.) and/or inorganic ions. The role of phenolic acids as allelopathic agents should not be neglected only based on their low specific concentrations in natural soils, because numbers and interactions of phenolic acids will increase their allelopathic activities.

  7. Spectroscopic elucidation of energy transfer in hybrid inorganic-biological organisms for solar-to-chemical production.

    Science.gov (United States)

    Kornienko, Nikolay; Sakimoto, Kelsey K; Herlihy, David M; Nguyen, Son C; Alivisatos, A Paul; Harris, Charles B; Schwartzberg, Adam; Yang, Peidong

    2016-10-18

    The rise of inorganic-biological hybrid organisms for solar-to-chemical production has spurred mechanistic investigations into the dynamics of the biotic-abiotic interface to drive the development of next-generation systems. The model system, Moorella thermoacetica-cadmium sulfide (CdS), combines an inorganic semiconductor nanoparticle light harvester with an acetogenic bacterium to drive the photosynthetic reduction of CO2 to acetic acid with high efficiency. In this work, we report insights into this unique electrotrophic behavior and propose a charge-transfer mechanism from CdS to M. thermoacetica Transient absorption (TA) spectroscopy revealed that photoexcited electron transfer rates increase with increasing hydrogenase (H2ase) enzyme activity. On the same time scale as the TA spectroscopy, time-resolved infrared (TRIR) spectroscopy showed spectral changes in the 1,700-1,900-cm(-1) spectral region. The quantum efficiency of this system for photosynthetic acetic acid generation also increased with increasing H2ase activity and shorter carrier lifetimes when averaged over the first 24 h of photosynthesis. However, within the initial 3 h of photosynthesis, the rate followed an opposite trend: The bacteria with the lowest H2ase activity photosynthesized acetic acid the fastest. These results suggest a two-pathway mechanism: a high quantum efficiency charge-transfer pathway to H2ase generating H2 as a molecular intermediate that dominates at long time scales (24 h), and a direct energy-transducing enzymatic pathway responsible for acetic acid production at short time scales (3 h). This work represents a promising platform to utilize conventional spectroscopic methodology to extract insights from more complex biotic-abiotic hybrid systems.

  8. ATR-FTIR characterization of organic functional groups and inorganic ions in ambient aerosols at a rural site

    Science.gov (United States)

    Coury, Charity; Dillner, Ann M.

    An Attenuated Total Reflectance-Fourier Transform Infrared (ATR-FTIR) spectroscopic method was used to measure organic functional groups and inorganic ions at Tonto National Monument (TNM), an Interagency Monitoring of Protected Visual Environments (IMPROVE) sampling site in a rural area near Phoenix, Arizona. Functional groups and ions from common aerosol compound classes such as aliphatic and aromatic CH, methylene, methyl, aldehydes/ketones, carboxylic acids, ammonium sulfate and nitrate as well as functional groups from difficult to measure compound classes such as esters/lactones, acid anhydrides, carbohydrate hydroxyl and ethers, amino acids, and amines were quantified. On average, ˜33% of the PM 1.0 mass was composed of organic aerosol. The average (standard deviation) composition of the organic aerosol at TNM was 34% (6%) biogenic functional groups, 21% (5%) oxygenated functional groups, 28% (7%) aliphatic hydrocarbon functional groups (aliphatic CH, methylene and methyl) and 17% (1%) aromatic hydrocarbon functional groups. Compositional analysis, functional group correlations, and back trajectories were used to identify three types of events with source signatures: primary biogenic-influenced, urban-influenced, and regional background. The biogenic-influenced event had high concentrations of amino acids and carbohydrate hydroxyl and ether, as well as aliphatic CH and aromatic CH functional groups and qualitatively high levels of silicate. The urban-influenced events had back trajectories traveling directly from the Phoenix area and high concentrations of hydrocarbons, oxygenated functional groups, and inorganic ions. This aerosol characterization suggests that both primary emissions in Phoenix and secondary formation of aerosols from Phoenix emissions had a major impact on the aerosol composition and concentration at TNM. The regional background source had low concentrations of all functional groups, but had higher concentrations of biogenic functional

  9. 2010 INORGANIC CHEMISTRY GORDON RESEARCH CONFERENCE JUNE 20 - 25, 2010

    Energy Technology Data Exchange (ETDEWEB)

    JOHN LOCKEMEYER

    2010-06-25

    The Inorganic Chemistry GRC is one of the longest-standing of the GRCs, originating in 1951. Over the years, this conference has played a role in spawning many other GRCs in specialized fields, due to the involvement of elements from most of the periodic table. These include coordination, organometallic, main group, f-element, and solid state chemistries; materials science, catalysis, computational chemistry, nanotechnology, bioinorganic, environmental, and biomedical sciences just to name a few. The 2010 Inorganic Chemistry GRC will continue this tradition, where scientists at all levels from academic, industrial, and national laboratories meet to define the important problems in the field and to highlight emerging opportunities through exchange of ideas and discussion of unpublished results. Invited speakers will present on a wide variety of topics, giving attendees a look at areas both inside and outside of their specialized areas of interest. In addition to invited speakers, the poster sessions at GRCs are a key feature of the conference. All conferees at the Inorganic Chemistry GRC are invited to present a poster on their work, and here the informal setting promotes the free exchange of ideas and fosters new relationships. As in previous years, we will offer poster presenters the opportunity to compete for one of several program spots in which they can give an oral presentation based on the subject matter of their poster. This is a great way to get your work noticed by the scientists attending the meeting, especially for those early in their career path such as junior faculty members, postdoctoral fellows, and those at comparable ranks. Anyone interested in participating in the poster competition should bring an electronic slide presentation and a small hard copy of their poster to submit to the committee.

  10. NOVEL INORGANIC MEMBRANES FOR HIGH TEMPERATURE CARBON DIOXIDE SEPARATION

    Energy Technology Data Exchange (ETDEWEB)

    Jerry Y.S. Lin

    2003-02-01

    We studied feasibility of two types of dense inorganic membranes which are fundamentally different from those porous inorganic membranes reported in the literature for separation of carbon dioxide from gas streams at high temperatures. The first is a symmetric, dense membrane made of Li{sub 2}ZrO{sub 3} and the second is a dual-phase metal-carbonate membrane. We have identified a unique CO{sub 2} sorption/desorption mechanism on lithium zirconate. Considering the all obtained data, we proposed a double layer model to describe the CO{sub 2} sorption/desorption behavior of lithium zirconate. In the model, final product after CO{sub 2} sorption is a particle which consists of a ZrO{sub 2} core inside and a Li{sub 2}CO{sub 3} shell. The understanding of CO{sub 2} sorption mechanisms suggests a means to improve CO{sub 2} sorption rate on this group of oxides. It also leads to the conclusion that lithium zirconate is not a suitable material for the proposed dense ceramic membrane for CO{sub 2} separation. Following the second concept of dense membrane for CO{sub 2} separation, we succeeded in preparing the hermetic (gas-tight) dense inorganic membrane consisting of a porous metal phase and a molten carbonate phase. The metal phase not only provides the mechanical support but also is electronically conducting, reducing the overall mass transfer resistance for CO{sub 2} permeation through the membrane. Permeation data showed that nitrogen or helium is not permeable through these membranes (only CO{sub 2}, with O{sub 2}, can permeate through the membrane based on the transport mechanism). This dual-phase membrane may offer promising properties for applications in membrane processes for separation of CO{sub 2} from flue (or coal gasification gas) at high temperatures (350-550 C).

  11. Linking calcification by exotic snails to stream inorganic carbon cycling.

    Science.gov (United States)

    Hotchkiss, Erin R; Hall, Robert O

    2010-05-01

    Biotic calcification is rarely considered in freshwater C budgets, despite calculations suggesting that calcifying animals can alter inorganic C cycling. Most studies that have quantified biocalcification in aquatic ecosystems have not directly linked CO(2) fluxes from biocalcification with whole-ecosystem rates of inorganic C cycling. The freshwater snail, Melanoides tuberculata, has achieved a high abundance and 37.4 g biomass m(-2) after invading Kelly Warm Springs in Grand Teton National Park. This high biomass suggests that introduced populations of Melanoides may alter ecosystem processes. We measured Melanoides growth rates and biomass to calculate the production of biomass, shell mass, and CO(2). We compared Melanoides biomass and inorganic C production with ecosystem C pools and fluxes, as well as with published rates of CO(2) production by other calcifying organisms. Melanoides calcification in Kelly Warm Springs produced 12.1 mmol CO(2) m(-2) day(-1) during summer months. We measured high rates of gross primary productivity and respiration in Kelly Warm Springs (-378 and 533 mmol CO(2) m(-2) day(-1), respectively); CO(2) produced from biocalcification increased net CO(2) production in Kelly Warm Springs from 155 to 167 mmol CO(2) m(-2) day(-1). This rate of CO(2) production via biocalcification is within the published range of calcification by animals. But these CO(2) fluxes are small when compared to ecosystem C fluxes from stream metabolism. The influence of animals is relative to ecosystem processes, and should always be compared with ecosystem fluxes to quantify the importance of a specific animal in its environment.

  12. An Experimental Method to Quantify Extractable Amino Acids in Soils from Southeast China

    Institute of Scientific and Technical Information of China (English)

    CHEN Xian-you; WU Liang-huan; CAO Xiao-chuang; Sarkar Animesh; ZHU Yuan-hong

    2013-01-01

    The extraction and comparison of soil amino acids using different extractants (deionized water, K2SO4, Na2SO4, NaCl, KCl) were reported. Results showed that 0.5 mol L-1 K2SO4 with a 5 times extraction was a better method to assess the concentration of extractable amino acids in soils. The total amino acids extracted from soil planted for tea were similar to the total inorganic nitrogen. While they extracted from vegetable soil and paddy soil were much lower than the total inorganic nitrogen.

  13. Optical Properties of Photovoltaic Organic-Inorganic Lead Halide Perovskites.

    Science.gov (United States)

    Green, Martin A; Jiang, Yajie; Soufiani, Arman Mahboubi; Ho-Baillie, Anita

    2015-12-03

    Over the last several years, organic-inorganic lead halide perovskites have rapidly emerged as a new photovoltaic contender. Although energy conversion efficiency above 20% has now been certified, improved understanding of the material properties contributing to these high performance levels may allow the progression to even higher efficiency, stable cells. The optical properties of these new materials are important not only to device design but also because of the insight they provide into less directly accessible properties, including energy-band structures, binding energies, and likely impact of excitons, as well as into absorption and inverse radiative recombination processes.

  14. Rational design of inorganic dielectric materials with expected permittivity

    Science.gov (United States)

    Xie, Congwei; Oganov, Artem R.; Dong, Dong; Liu, Ning; Li, Duan; Debela, Tekalign Terfa

    2015-11-01

    Techniques for rapid design of dielectric materials with appropriate permittivity for many important technological applications are urgently needed. It is found that functional structure blocks (FSBs) are helpful in rational design of inorganic dielectrics with expected permittivity. To achieve this, coordination polyhedra are parameterized as FSBs and a simple empirical model to evaluate permittivity based on these FSB parameters is proposed. Using this model, a wide range of examples including ferroelectric, high/low permittivity materials are discussed, resulting in several candidate materials for experimental follow-up.

  15. Annual reports in inorganic and general syntheses 1976

    CERN Document Server

    Zimmer, Hans

    2013-01-01

    Annual Reports in Inorganic and General Syntheses-1976 presents an annual review of synthetically useful information that would prove beneficial to nearly all organic chemists, both specialist and nonspecialist in synthesis. It should help relieve some of the information storage burden of the specialist and should aid the nonspecialist who is seeking help with a specific problem to become rapidly aware of recent synthetic advances.This is the fifth volume of ARIGS and is organized along the lines developed for the preceding volumes. The authors were encouraged to use synthetic aspects as their

  16. Modified inorganic surfaces as a model for hydroxyapatite growth

    CERN Document Server

    Pramatarova, Lilyana

    2006-01-01

    The process by which organisms in Nature create minerals is known as biomineralization - a process that involves complex interactions between inorganic ions, crystals and organic molecules; resulting in a controlled nucleation and growth of minerals from aqueous solutions. During the last few decades, biomineralization has been intensively studied, due to its involvement in a wide range of biological events; starting with the formation of bones, teeth, cartilage, shells, coral (so-called physiological mineralization) and encompassing pathological mineralization, i.e. the formation of kidney st

  17. Synthesis, Properties and Mineralogy of Important Inorganic Materials

    CERN Document Server

    Warner, Terence E

    2010-01-01

    Intended as a textbook for courses involving preparative solid-state chemistry, this book offers clear and detailed descriptions on how to prepare a selection of inorganic materials that exhibit important optical, magnetic and electrical properties, on a laboratory scale. The text covers a wide range of preparative methods and can be read as separate, independent chapters or as a unified coherent body of work. Discussions of various chemical systems reveal how the properties of a material can often be influenced by modifications to the preparative procedure, and vice versa. References to miner

  18. Organic/inorganic hybrid materials: challenges for ab initio methodology.

    Science.gov (United States)

    Draxl, Claudia; Nabok, Dmitrii; Hannewald, Karsten

    2014-11-18

    CONSPECTUS: Organic/inorganic hybrid structures are most exciting since one can expect new properties that are absent in either of their building blocks. They open new perspectives toward the design and tailoring of materials with desired features and functions. Prerequisite for real progress is, however, the in-depth understanding of what happens on the atomic and electronic scale. In this respect, hybrid materials pose a challenge for electronic-structure theory. Methods that proved useful for describing one side may not be applicable for the other one, and they are likely to fail for the interfaces. In this Account, we address the question to what extent we can quantitatively describe hybrid materials and where we even miss a qualitative description. We note that we are dealing with extended systems and thus adopt a solid-state approach. Therefore, density-functional theory (DFT) and many-body perturbation theory (MBPT), the GW approach for charged and the Bethe-Salpeter equation for neutral excitations, are our methods of choice. We give a brief summary of the used methodology, focusing on those aspects where problems can be expected when materials of different character meet at an interface. These issues are then taken up when discussing hybrid materials. We argue when and why, for example, standard DFT may fall short when it comes to the electronic structure of organic/metal interfaces or where the framework of MBPT can or must take over. Selected examples of organic/inorganic interfaces, structural properties, electronic bands, optical excitation spectra, and charge-transport properties as obtained from DFT and MBPT highlight which properties can be reliably computed for such materials. The crucial role of van der Waals forces is shown for sexiphenyl films, where the subtle interplay between intermolecular and molecule-substrate interactions is decisive for growth and morphologies. With a PTCDA monolayer on metal surfaces we discuss the performance of DFT in

  19. Simultaneous determination of inorganic and organic anions by ion chromatography

    Energy Technology Data Exchange (ETDEWEB)

    Park, Yang Soon; Joe, Ki Soo; Han, Sun Ho; Park, Soon Dal; Choi, Kwang Soon

    1999-06-01

    Four methods were investigated for the simultaneous determination of several inorganic and organic anions in aqueous solution by ion chromatography. The first is two columns coupled system. The second is the gradient elution system with an anion exchange column. The third is the system with a mixed-mode stationary phase. The fourth is the system with an anion exchange column and the eluant of low conductivity without ion suppressor. The advantages and disadvantages of individual systems were discussed. The suitable methods were proposed for the application to the samples of the nuclear power industry and the environment. (author)

  20. Inorganic Chemistry in Hydrogen Storage and Biomass Catalysis

    Energy Technology Data Exchange (ETDEWEB)

    Thorn, David [Los Alamos National Laboratory

    2012-06-13

    Making or breaking C-H, B-H, C-C bonds has been at the core of catalysis for many years. Making or breaking these bonds to store or recover energy presents us with fresh challenges, including how to catalyze these transformations in molecular systems that are 'tuned' to minimize energy loss and in molecular and material systems present in biomass. This talk will discuss some challenging transformations in chemical hydrogen storage, and some aspects of the inorganic chemistry we are studying in the development of catalysts for biomass utilization.

  1. Inorganic arrangement crystal beryllium, lithium, selenium and silicon

    CERN Document Server

    Gobato, Ricardo; Fedrigo, Desire Francine Gobato

    2015-01-01

    The use of inorganic crystals technology has been widely date. Since quartz crystals for watches in the nineteenth century, and common way radio in the early twentieth century, to computer chips with new semiconductor materials. Chemical elements such as beryllium, lithium, selenium and silicon, are widely used in technology. The development of new crystals arising from that arrangement can bring technological advances in several areas of knowledge. The likely difficulty of finding such crystals in nature or synthesized, suggest an advanced study of the subject. A study using computer programs with ab initio method was applied. As a result of the likely molecular structure of the arrangement of a crystal was obtained.

  2. Influence of inorganic salt on aerobic biodegradability of dyestuffs

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    this paper, the influence of inorganic salt on aerobic biodegradability of dyestuffs was studied by means of semicontinuous activated sludge method. It was found that: biodegradability of dyestuffs would decrease with the increase of the concentration of NaCl; however, biodegradability in the condition of NaCl = 30 g/L was better than that in the condition of NaCl =15 g/L; in the three NaCl conditions, biodegradability of tasted dyestuffs followed the following order: NaCl= 0 g/L > NaCl= 30g/L>NaCl= 15 g/L.

  3. Inorganic arsenic impairs differentiation and functions of human dendritic cells

    Energy Technology Data Exchange (ETDEWEB)

    Macoch, Mélinda; Morzadec, Claudie [UMR INSERM U1085, Institut de Recherche sur la Santé, l' Environnement et le Travail (IRSET), Université de Rennes 1, 2 avenue du Professeur Léon Bernard, 35043 Rennes (France); Fardel, Olivier [UMR INSERM U1085, Institut de Recherche sur la Santé, l' Environnement et le Travail (IRSET), Université de Rennes 1, 2 avenue du Professeur Léon Bernard, 35043 Rennes (France); Pôle Biologie, Centre Hospitalier Universitaire (CHU) Rennes, 2 rue Henri Le Guilloux, 35033 Rennes (France); Vernhet, Laurent, E-mail: laurent.vernhet@univ-rennes1.fr [UMR INSERM U1085, Institut de Recherche sur la Santé, l' Environnement et le Travail (IRSET), Université de Rennes 1, 2 avenue du Professeur Léon Bernard, 35043 Rennes (France)

    2013-01-15

    Experimental studies have demonstrated that the antileukemic trivalent inorganic arsenic prevents the development of severe pro-inflammatory diseases mediated by excessive Th1 and Th17 cell responses. Differentiation of Th1 and Th17 subsets is mainly regulated by interleukins (ILs) secreted from dendritic cells (DCs) and the ability of inorganic arsenic to impair interferon-γ and IL-17 secretion by interfering with the physiology of DCs is unknown. In the present study, we demonstrate that high concentrations of sodium arsenite (As(III), 1–2 μM) clinically achievable in plasma of arsenic-treated patients, block differentiation of human peripheral blood monocytes into immature DCs (iDCs) by inducing their necrosis. Differentiation of monocytes in the presence of non-cytotoxic concentrations of As(III) (0.1 to 0.5 μM) only slightly impacts endocytotic activity of iDCs or expression of co-stimulatory molecules in cells activated with lipopolysaccharide. However, this differentiation in the presence of As(III) strongly represses secretion of IL-12p70 and IL-23, two major regulators of Th1 and Th17 activities, from iDCs stimulated with different toll-like receptor (TLR) agonists in metalloid-free medium. Such As(III)-exposed DCs also exhibit reduced mRNA levels of IL12A and/or IL12B genes when activated with TLR agonists. Finally, differentiation of monocytes with non-cytotoxic concentrations of As(III) subsequently reduces the ability of activated DCs to stimulate the release of interferon-γ and IL-17 from Th cells. In conclusion, our results demonstrate that clinically relevant concentrations of inorganic arsenic markedly impair in vitro differentiation and functions of DCs, which may contribute to the putative beneficial effects of the metalloid towards inflammatory autoimmune diseases. Highlights: ► Inorganic arsenic impairs differentiation and functions of human dendritic cells (DCs) ► Arsenite (> 1 μM) blocks differentiation of dendritic cells by

  4. Multi length-scale characterisation inorganic materials series

    CERN Document Server

    Bruce, Duncan W; Walton, Richard I

    2013-01-01

    Whereas the first five volumes in the Inorganic Materials Series focused on particular classes of materials (synthesis, structures, chemistry, and properties), it is now very timely to provide complementary volumes that introduce and review state-of-the-art techniques for materials characterization. This is an important way of emphasizing the interplay of chemical synthesis and physical characterization. The methods reviewed include spectroscopic, diffraction, and surface techniques that examine the structure of materials on all length scales, from local atomic structure to long-range crystall

  5. Design of targeting ligands in medicinal inorganic chemistry.

    Science.gov (United States)

    Storr, Tim; Thompson, Katherine H; Orvig, Chris

    2006-06-01

    This tutorial review will highlight recent advances in medicinal inorganic chemistry pertaining to the use of multifunctional ligands for enhanced effect. Ligands that adequately bind metal ions and also include specific targeting features are gaining in popularity due to their ability to enhance the efficacy of less complicated metal-based agents. Moving beyond the traditional view of ligands modifying reactivity, stabilizing specific oxidation states, and contributing to substitution inertness, we will discuss recent work involving metal complexes with multifunctional ligands that target specific tissues, membrane receptors, or endogenous molecules, including enzymes.

  6. Tetraalkylphosphonium polyoxometalate ionic liquids : novel, organic-inorganic hybrid materials.

    Energy Technology Data Exchange (ETDEWEB)

    Rickert, P. G.; Antonio, M. P.; Firestone, M. A.; Kubatko, K.-A.; Szreder, T.; Wishart, J. F.; Dietz, M. L.; Chemistry; Univ. of Notre Dame; BNL

    2007-01-01

    Pairing of a Keggin or Lindqvist polyoxometalate (POM) anion with an appropriate tetraalkylphosphonium cation is shown to yield the first members of a new family of ionic liquids (ILs). Detailed characterization of one of them, an ambient-temperature 'liquid POM' comprising the Lindqvist salt of the trihexyl(tetradecyl) phosphonium cation, by voltammetry, viscometry, conductimetry, and thermal analysis indicates that it exhibits conductivity and viscosity comparable to those of the one previously described inorganic-organic POM-IL hybrid but with substantially improved thermal stability.

  7. Engineering the Interface Between Inorganic Materials and Cells

    Energy Technology Data Exchange (ETDEWEB)

    Schaffer, David

    2014-05-31

    To further optimize cell function in hybrid “living materials”, it would be advantageous to render mammalian cells responsive to novel “orthogonal” cues, i.e. signals they would not ordinarily respond to but that can be engineered to feed into defined intracellular signaling pathways. We recently developed an optogenetic method, based on A. thaliana Cry2, for rapid and reversible protein oligomerization in response to blue light. We also demonstrated the ability to use this method to channel the light input into several defined signaling pathways, work that will enhance communication between inorganic devices and living systems.

  8. Tetraalkylphosphonium polyoxometalate ionic liquids: novel, organic-inorganic hybrid materials.

    Science.gov (United States)

    Rickert, Paul G; Antonio, Mark R; Firestone, Millicent A; Kubatko, Karrie-Ann; Szreder, Tomasz; Wishart, James F; Dietz, Mark L

    2007-05-10

    Pairing of a Keggin or Lindqvist polyoxometalate (POM) anion with an appropriate tetraalkylphosphonium cation is shown to yield the first members of a new family of ionic liquids (ILs). Detailed characterization of one of them, an ambient-temperature "liquid POM" comprising the Lindqvist salt of the trihexyl(tetradecyl) phosphonium cation, by voltammetry, viscometry, conductimetry, and thermal analysis indicates that it exhibits conductivity and viscosity comparable to those of the one previously described inorganic-organic POM-IL hybrid but with substantially improved thermal stability.

  9. Sol-gel Synthesis of a Biotemplated Inorganic Photocatalyst

    DEFF Research Database (Denmark)

    Boffa, Vittorio; Yue, Yuanzheng; He, Wen

    2012-01-01

    As part of a laboratory course, undergraduate students were asked to use baker’s yeast cells as biotemplate in preparing TiO2 powders and to test the photocatalytic activity of the resulting materials. This laboratory experience, selected because of the important environmental implications of soft...... chemistry and photocatalysis, provides an opportunity to teach valuable laboratory skills and to introduce students to the synthesis, isolation, and characterization of inorganic materials. This laboratory activity is adaptable to a range of educational levels and to various instrumental techniques....

  10. Standard Electrode Potentials Involving Radicals in Aqueous Solution: Inorganic Radicals

    Energy Technology Data Exchange (ETDEWEB)

    Armstrong, David A.; Huie, Robert E.; Koppenol, Willem H.; Lymar, Sergei V.; Merenyi, Gabor; Neta, Pedatsur; Ruscic, Branko; Stanbury, David M.; Steenken, Steen; Wardman, Peter

    2015-12-01

    Recommendations are made for standard potentials involving select inorganic radicals in aqueous solution at 25 °C. These recommendations are based on a critical and thorough literature review and also by performing derivations from various literature reports. The recommended data are summarized in tables of standard potentials, Gibbs energies of formation, radical pKa’s, and hemicolligation equilibrium constants. In all cases, current best estimates of the uncertainties are provided. An extensive set of Data Sheets is appended that provide original literature references, summarize the experimental results, and describe the decisions and procedures leading to each of the recommendations

  11. All inorganic semiconductor nanowire mesh for direct solar water splitting.

    Science.gov (United States)

    Liu, Bin; Wu, Cheng-Hao; Miao, Jianwei; Yang, Peidong

    2014-11-25

    The generation of chemical fuels via direct solar-to-fuel conversion from a fully integrated artificial photosynthetic system is an attractive approach for clean and sustainable energy, but so far there has yet to be a system that would have the acceptable efficiency, durability and can be manufactured at a reasonable cost. Here, we show that a semiconductor mesh made from all inorganic nanowires can achieve unassisted solar-driven, overall water-splitting without using any electron mediators. Free-standing nanowire mesh networks could be made in large scales using solution synthesis and vacuum filtration, making this approach attractive for low cost implementation.

  12. Inorganic salt mixtures as electrolyte media in fuel cells

    Science.gov (United States)

    Angell, Charles Austen (Inventor); Belieres, Jean-Philippe (Inventor); Francis-Gervasio, Dominic (Inventor)

    2012-01-01

    Fuel cell designs and techniques for converting chemical energy into electrical energy uses a fuel cell are disclosed. The designs and techniques include an anode to receive fuel, a cathode to receive oxygen, and an electrolyte chamber in the fuel cell, including an electrolyte medium, where the electrolyte medium includes an inorganic salt mixture in the fuel cell. The salt mixture includes pre-determined quantities of at least two salts chosen from a group consisting of ammonium trifluoromethanesulfonate, ammonium trifluoroacetate, and ammonium nitrate, to conduct charge from the anode to the cathode. The fuel cell includes an electrical circuit operatively coupled to the fuel cell to transport electrons from the cathode.

  13. Effects of organic and inorganic additives on flotation recovery of washed cells of Saccharomyces cerevisiae resuspended in water.

    Science.gov (United States)

    DeSousa, Sandro Rogério; Laluce, Cecilia; Jafelicci, Miguel

    2006-03-01

    Separation of microbial cells by flotation recovery is usually carried out in industrial reactors or wastewater treatment systems, which contain a complex mixture of microbial nutrients and excretion products. In the present study, the separation of yeast cells by flotation recovery was carried out using a simple flotation recovery systems containing washed yeast cells resuspended in water in order to elucidate the effects of additives (defined amounts of organic and inorganic acids, ethanol, surfactants and sodium chloride) on the cellular interactions at interfaces (cell/aqueous phase and cell/air bubble). When sodium chloride, organic acids (notably propionic, succinic and acetic acids) and organic surfactants (sodium dodecyl sulphate (SDS), cetyltrimethylammonium bromide (CTAB) and Nonidet P40) were added to the flotation recovery system, significant increases in the cell recovery of yeast hydrophobic cells (Saccharomyces cerevisiae, strain FLT-01) were observed. The association of ethanol to acetic acid solution (a minor by-product of alcoholic fermentation) in the flotation recovery system, containing washed cells of strain FLT-01 resuspended in water, leading to an increased flotation recovery at pH 5.5. Thus, the association among products of the cellular metabolism (e.g., ethanol and acetic acid) can improve yeast cell recovery by flotation recovery.

  14. Feeding low-phytic acid corn grain to finishing wethers does not alter phosphorus digestion

    Science.gov (United States)

    Low-phytic acid (LPA) feed grains contain similar concentrations of P as do standard grains, but the majority of P exists as inorganic phosphate rather than phytic acid. Research has shown that LPA feeds can be used to improve overall efficiency of P utilization in swine, poultry and aquaculture pro...

  15. The rice OsLpa1 gene encodse a novel protein involved in phytic acid metabolism

    Science.gov (United States)

    The rice low phytic acid 1 (OsLpa1) gene was originally identified using a forward genetics approach. Mutation of this gene resulted in a 45% reduction in rice seed phytic acid with a molar-equivalent increase in inorganic phosphorus; however, the rice lpa1 mutant does not appear to differ significa...

  16. Acid and organic aerosol coatings on magnetic nanoparticles increase iron concentrations in human airway epithelial cells.

    Science.gov (United States)

    Ghio, Andrew J; Dailey, Lisa A; Richards, Judy H; Jang, Myoseon

    2009-07-01

    Numerous industrial applications for man-made nanoparticles have been proposed. Interactions of nanoparticles with agents in the atmosphere may impact human health. We tested the postulate that in vitro exposures of respiratory epithelial cells to airborne magnetic nanoparticles (MNP; Fe(3)O(4)) with and without a secondary organic aerosol (SOA) and an inorganic acid could affect iron homeostasis, oxidative stress, and interleukin (IL)-8 release. Cell iron concentrations were increased after exposures to MNP and values were further elevated with co-exposures to either SOA or inorganic acid. Increased expression of ferritin and elevated levels of RNA for DMT1, proteins for iron storage and transport respectively, followed MNP exposures, but values were significant for only those with co-exposures to inorganic acid and organic aerosols. Cell iron concentration corresponded to a measure of oxidative stress in the airway epithelial cells; MNP with co-exposures to SOA and inorganic acid increased both available metal and indices of oxidant generation. Finally, the release of a proinflammatory cytokine (i.e. IL-8) by the exposed cells similarly increased with cell iron concentration. We conclude that MNP can interact with a SOA and an inorganic acid to present metal in a catalytically reactive state to cultured respiratory cells. This produces an oxidative stress to affect a release of IL-8.

  17. Metal-free inorganic ligands for colloidal nanocrystals: S2-, HS-, Se2-, HSe-, Te2-, HTe-, TeS3(2-), OH-, and NH2- as surface ligands.

    Science.gov (United States)

    Nag, Angshuman; Kovalenko, Maksym V; Lee, Jong-Soo; Liu, Wenyong; Spokoyny, Boris; Talapin, Dmitri V

    2011-07-13

    All-inorganic colloidal nanocrystals were synthesized by replacing organic capping ligands on chemically synthesized nanocrystals with metal-free inorganic ions such as S(2-), HS(-), Se(2-), HSe(-), Te(2-), HTe(-), TeS(3)(2-), OH(-) and NH(2)(-). These simple ligands adhered to the NC surface and provided colloidal stability in polar solvents. The versatility of such ligand exchange has been demonstrated for various semiconductor and metal nanocrystals of different size and shape. We showed that the key aspects of Pearson's hard and soft acids and bases (HSAB) principle, originally developed for metal coordination compounds, can be applied to the bonding of molecular species to the nanocrystal surface. The use of small inorganic ligands instead of traditional ligands with long hydrocarbon tails facilitated the charge transport between individual nanocrystals and opened up interesting opportunities for device integration of colloidal nanostructures.

  18. Organic-inorganic hybrid membranes in separation processes: a 10-year review

    Directory of Open Access Journals (Sweden)

    V. C. Souza

    2013-12-01

    Full Text Available In relation to some inorganic membranes, polymeric membranes have relatively low separation performance. However, the processing flexibility and low cost of polymers still make them highly attractive for many industrial separation applications. Polymer-inorganic hybrid membranes constitute an emerging research field and have been recently developed to improve the separation properties of polymer membranes because they possess properties of both organic and inorganic membranes such as good hydrophilicity, selectivity, permeability, mechanical strength, and thermal and chemical stability. The structures and processing of polymer-inorganic nanocomposite hybrid membranes, as well as their use in the fields of ultrafiltration, nanofiltration, pervaporation, gas separation and separation mechanism are reviewed.

  19. Folic acid

    Science.gov (United States)

    ... taking folic acid by itself, or with L-carnitine a compound similar to an amino acid from ... levels. It is not clear if folic acid supplementation reduces hearing loss in people with normal folate ...

  20. The behavior of dissolved inorganic selenium in the Changjiang Estuary

    Science.gov (United States)

    Chang, Yan; Zhang, Jing; Qu, Jianguo; Zhang, Guosen; Zhang, Anyu; Zhang, Ruifeng

    2016-02-01

    To investigate the behavior of inorganic selenium species in the Changjiang Estuary, samples were taken during summer (July 2011) and winter (March 2012). Dissolved inorganic selenium (DISe) concentrations averaged 1.79 nmol/L in summer and 1.24 nmol/L in winter; the average selenite [Se(IV)] to selenate [Se(VI)] ratio [Se(IV)/Se(VI)] was 0.42 in summer and 0.61 in winter. The data show that Se(IV) and Se(VI) concentrations in the estuary behaved strictly conservatively during winter but non-conservatively during summer due to adsorption by suspended particulate matter (SPM) and assimilation by phytoplankton. In addition, the Se concentration distributions in the Changjiang Estuary were controlled by three water masses, each with a specific Se(IV)/Se(VI) ratio "signature": the Changjiang Water input, the Taiwan Warm Current, and the Yellow Sea Coastal Current. The Se(IV) concentrations were related to the nitrate, silicate, and phosphate concentrations in the estuary. The DISe and Se(IV) concentrations were comparable to those found in other coastal regions and estuaries, which were considered to be natural levels.