WorldWideScience

Sample records for non-metallic inorganic compounds

  1. 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.

  2. Microbiological disproportionation of inorganic sulfur compounds

    DEFF Research Database (Denmark)

    Finster, Kai

    2008-01-01

    The disproportionation of inorganic sulfur intermediates at moderate temperatures (0-80 °C) is a microbiologically catalyzed chemolithotrophic process in which compounds like elemental sulfur, thiosulfate, and sulfite serve as both electron donor and acceptor, and generate hydrogen sulfide...... or phototrophic sulfide oxidizers. Investigations bridging geology and microbiology have found strong evidence for disproportionating bacteria participating in and enhancing the rate at which pyrite forms and being partly responsible for the isotopic signatures of sulfidic minerals in recent and old sediments...

  3. Triboelectric separation technology for removing inorganics from non-metallic fraction of waste printed circuit boards: Influence of size fraction and process optimization.

    Science.gov (United States)

    Zhang, Guangwen; Wang, Haifeng; He, Yaqun; Yang, Xing; Peng, Zhen; Zhang, Tao; Wang, Shuai

    2017-02-01

    Removing inorganics from non-metallic fraction (NMF) of waste printed circuit boards (WPCBs) is an effective mean to improve its usability. The effect of size fraction on the triboelectric separation of NMF of WPCBs was investigated in a lab triboelectric separation system and the separation process was optimized in this paper. The elements distribution in raw NMF collected from typical WPCBs recycling plant and each size fraction obtained by sieving were analyzed by X-ray fluorescence (XRF). The results show that the main inorganic elements in NMF are P, Ba, Mn, Sb, Ti, Pb, Zn, Sn, Mg, Fe, Ca, Cu, Al and Si. The inorganic content of each size fraction increased with the size decreasing. The metal elements are mainly distributed in -0.2mm size fraction, and concentrated in middle product of triboelectric separation. The loss on ignition (LOI) of positive product and negative product is higher than that of the middle product for the -0.355mm size fraction, while the LOI presents gradually increasing trend from negative to positive plate for the +0.355mm size fraction. Based on the separation results and mineralogical characterizations of each size fraction of NMF, the pretreatment process including several mineral processing operations was added before triboelectric separation and better separation result was obtained. Copyright © 2016 Elsevier Ltd. All rights reserved.

  4. 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.

  5. Investigations on organogermanium compounds XII. Reactions of trialkylgermylalkalimetal compounds in hexamethylphosphoric triamide (HMPT) with some inorganic and organic compounds

    NARCIS (Netherlands)

    Bulten, E.J.; Noltes, J.G.

    1971-01-01

    Trialkylgermyl alkali metal compounds in HMPT have been found to be highly reactive nucleophiles. Reactions with some inorganic and organic compounds, such as oxygen, carbon dioxide, inorganic and orgaanic halides, aldehydes, ketones, epoxides and lactones are described. Several new

  6. Binary systems solubilities of inorganic and organic compounds

    CERN Document Server

    Stephen, H

    1963-01-01

    Solubilities of Inorganic and Organic Compounds, Volume 1: Binary Systems, Part 1 is part of an approximately 5,500-page manual containing a selection from the International Chemical Literature on the Solubilities of Elements, Inorganic Compounds, Metallo-organic and Organic Compounds in Binary, Ternary and Multi-component Systems. A careful survey of the literature in all languages by a panel of scientists specially appointed for the task by the U.S.S.R. Academy of Sciences, Moscow, has made the compilation of this work possible. The complete English edition in five separately bound volumes w

  7. Investigations on organogermanium compounds XII. Reactions of trialkylgermylalkalimetal compounds in hexamethylphosphoric triamide (HMPT) with some inorganic and organic compounds

    NARCIS (Netherlands)

    Bulten, E.J.; Noltes, J.G.

    1971-01-01

    Trialkylgermyl alkali metal compounds in HMPT have been found to be highly reactive nucleophiles. Reactions with some inorganic and organic compounds, such as oxygen, carbon dioxide, inorganic and orgaanic halides, aldehydes, ketones, epoxides and lactones are described. Several new carbon-functiona

  8. 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.

  9. 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.

  10. 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.

  11. Kinetics of metabolism of organic and inorganic 14C compounds.

    Science.gov (United States)

    Vasilenko IYa; Bugryshev, P F; Istomina, A G; Turova, V I

    1982-01-01

    Results of experimental studies on the dynamics of metabolism of various inorganic (NA2CO3, K2CO3, CaCO3) and organic (glucose, glycine, palmitic and succinic acids, ethanol and methanol) compounds of 14C after its single and long-term administration into the organism of rats are presented. The values of the corresponding rates of accumulation of 14C and the onset of the state of equilibrium after long-term administration of the radionuclide were elucidated for a number of compounds. Results of the studies can find practical application in norm-setting. The corresponding rate of accumulation in man of 14C taken in the diet was determined by extrapolation of the experimental data. It was found to be approximately 30. The state of practical 14C equilibrium in man occurs approximately 11/2 years after the beginning of the intake.

  12. 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.

  13. Surface modification of inorganic layer compound with organic compound and preparation of thin films

    Science.gov (United States)

    Tagaya, Hideyuki; Morioka, Hiroyuki; Ogata, Sumikazu; Karasu, Masa; Kadokawa, Jun-ichi; Chiba, Koji

    1997-11-01

    Water treated Zn/Al layered double hydroxide (LDH) was prepared by the reaction of LDH oxide and water. By the reaction of the water treated Zn/Al LDH or amorphous metal hydroxide and organic oxychloride, surface modified inorganic layer compounds were prepared. Their layer structures were similar to those of the orginal LDHs except the reaction product of amorphous metal hydroxide and benzoyl chloride. Interlayer spacings of the reaction products were 0.77 to 2.67 nm depending on the size and number of function groups of organic compounds.

  14. Isostructural organic-inorganic hybrid compounds: triethylcholine tribromidocadmate and triethylcholine tribromidomercurate.

    Science.gov (United States)

    Wang, Dong-Yan; Hou, Xue-Li; Li, Xue-Nan

    2015-08-01

    In order to search for new anionic architectures and develop useful organic-inorganic hybrid materials in halometallate systems, two new crystalline organic-inorganic hybrid compounds have been prepared, i.e. catena-poly[triethyl(2-hydroxyethyl)azanium [[bromidocadmate(II)]-di-μ-bromido

  15. 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

  16. 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

  17. Separation of nonionic compounds by electrokinetic chromatography using an inorganic layered compound as a pseudostationary phase.

    Science.gov (United States)

    Koike, Ryo; Kitagawa, Fumihiko; Otsuka, Koji

    2008-03-01

    The use of an inorganic layered compound as a pseudostationary phase (PSP) in EKC was investigated. A synthetic smectite, which is the most typical swellable clay mineral, with an average diameter of 130 nm was selected as the PSP. The retention characteristics of the smectite and on-line sample concentration by sweeping were examined for the analysis of polyoxyethylene mono phenyl ethers (PPEs) with different degrees of ethoxylation. The retention factor was increased with increase in the number of ethylene oxide groups and a good separation of the PPE homologs was achieved by smectite-EKC. The RSD of the migration time, plate number, and peak area were 0.60, 8.3, and 2.7% (n = 5), respectively. The developed method can be applied to the analysis of PPEs in commercially available consumer products without any sample pretreatments. In addition, ca. 100-fold sensitivity enhancements for the PPEs with high retention factors were obtained by sweeping.

  18. Review on Insensitive Non-metallic Energetic Ionic Compounds of Tetrazolate Anions%不敏感四唑非金属含能离子化合物的研究进展

    Institute of Scientific and Technical Information of China (English)

    毕福强; 樊学忠; 许诚; 王伯周; 郑亚峰; 葛忠学; 刘庆

    2012-01-01

    四唑非金属含能离子化合物是近年来逐渐发展起来的一类新型不敏感含能材料.综述了以氨基四唑、硝基四唑、硝氨基四唑、偶氮四唑和呋咱取代四唑为阴离子的不敏感非金属含能离子化合物的研究进展,结果表明,5位连有硝基和硝氨基等传统含能基团的四唑离子化合物的感度普遍较高,而以氨基四唑、偶氮四唑和4-氨基-3-(四唑基)呋咱为阴离子的含能化合物有望在不敏感含能材料领域得到广泛应用,并进而提出了不敏感四唑非金属含能离子化合物研究的发展方向.%Non-metallic energetic ionic compounds of tetrazolate anion are a kind of insensitive energetic materials. The progresses in the insensitive non-metallic energetic salts of aminotetrazolate, nitrotetrazolate, nitraminotetrazolate, azotetrazolate and furazan fuctionalized tetrazolate anions were reviewed in detail. It is found that most of ionic compounds based on tetrazolate anions which contain traditional energetic functionalities upon the carbon of positon 5 such as nitro and nitrimino functionalities, show high sensitivities, while the sensitivities of ionic compounds based on 5-aminotetrazolate, 5, 5'-azotetrazolate and 5-(4-aminofurazan-3-yl)tetrazolate are so low that they can be used as insensitive energetic materials. Furthermore, new trends in research of insensitive non-metallic energetic ionic compounds of tetrazolate anion were proposed.

  19. Binary systems solubilities of inorganic and organic compounds, v.1 pt.2

    CERN Document Server

    Stephen, H

    2013-01-01

    Solubilities of Inorganic and Organic Compounds, Volume 1: Binary Systems, Part 1 is part of an approximately 5,500-page manual containing a selection from the International Chemical Literature on the Solubilities of Elements, Inorganic Compounds, Metallo-organic and Organic Compounds in Binary, Ternary and Multi-component Systems. A careful survey of the literature in all languages by a panel of scientists specially appointed for the task by the U.S.S.R. Academy of Sciences, Moscow, has made the compilation of this work possible. The complete English edition in five separately bound volumes w

  20. CHARACTERIZATION OF RADIATION GRAFT COPOLYMER OF INORGANIC COMPOUND ONTO ALKENE

    Institute of Scientific and Technical Information of China (English)

    ZhangWanxi; CheJitai; 等

    1995-01-01

    In this paper,the radiation graft copolymer of MgO,SiO2 and Y-molecular sieve onto organic compounds,such as methacrylate,styrene and acrylomitrile obtained by per-radiation method were characterized by X-ray diffraction,pyrolysis gas chromatography,GPC and X-ray photoelectron spectroscopy.

  1. Biological and chemical investigation of Allium cepa L. response to selenium inorganic compounds.

    Science.gov (United States)

    Michalska-Kacymirow, M; Kurek, E; Smolis, A; Wierzbicka, M; Bulska, E

    2014-06-01

    The aim of this study was to evaluate the biological and chemical response of Allium cepa L. exposed to inorganic selenium compounds. Besides the investigation of the total content of selenium as well as its chemical speciation, the Allium test was used to evaluate the growth of onion roots and mitotic activity in the roots' meristem. The total content of selenium was determined by inductively coupled plasma mass spectrometry (ICP MS). High-performance liquid chromatography (HPLC), coupled to ICP MS, was used for the selenium chemical speciation. Results indicated that A. cepa plants are able to biotransform inorganic selenium compounds into their organic derivatives, e.g., Se-methylselenocysteine from the Se(IV) inorganic precursor. Although the differences in the biotransformation of selenium are due mainly to the oxidation state of selenium, the experiment has also shown a fine effect of counter ions (H(+), Na(+), NH4 (+)) on the response of plants and on the specific metabolism of selenium.

  2. A golden future in medicinal inorganic chemistry : The promise of anticancer gold organometallic compounds

    NARCIS (Netherlands)

    Bertrand, B.; Casini, A.

    2014-01-01

    From wedding rings on fingers to stained glass windows, by way of Olympic medals, gold has been highly prized for millennia. Nowadays, organometallic gold compounds occupy an important place in the field of medicinal inorganic chemistry due to their unique chemical properties with respect to gold co

  3. A golden future in medicinal inorganic chemistry : The promise of anticancer gold organometallic compounds

    NARCIS (Netherlands)

    Bertrand, B.; Casini, A.

    2014-01-01

    From wedding rings on fingers to stained glass windows, by way of Olympic medals, gold has been highly prized for millennia. Nowadays, organometallic gold compounds occupy an important place in the field of medicinal inorganic chemistry due to their unique chemical properties with respect to gold co

  4. [Responses of rice-wheat rotation system in south Jiangsu to organic-inorganic compound fertilizers].

    Science.gov (United States)

    Tian, Heng-Da; Zhang, Li; Zhang, Jian-Chao; Wang, Qiu-Jun; Xu, Da-Bing; Yibati, Halihashi; Xu, Jia-Le; Huang, Qi-Wei

    2011-11-01

    In 2006-2007, a field trial was conducted to study the effects of applying three kinds of organic-inorganic compound fertilizers [rapeseed cake compost plus inorganic fertilizers (RCC), pig manure compost plus inorganic fertilizers (PMC), and Chinese medicine residues plus inorganic fertilizers (CMC)] on the crop growth and nitrogen (N) use efficiency of rice-wheat rotation system in South Jiangsu. Grain yield of wheat and rice in the different fertilization treatments was significantly higher than the control (no fertilization). In treatments RCC, PMC and CMC, the wheat yield was 13.1%, 32.2% and 39.3% lower than that of the NPK compound fertilizer (CF, 6760 kg x hm(-2)), respectively, but the rice yield (8504-9449 kg x hm(-2)) was significantly higher than that (7919 kg x hm(-2)) of CF, with an increment of 7.4%-19.3%. In wheat season, the aboveground dry mass, N accumulation, and N use efficiency in treatments RCC, PMC, and CMC were lower than those of CF, but in rice season, these parameters were significantly higher than or as the same as CF. In sum, all the test three compound fertilizers had positive effects on the rice yield and its nitrogen use efficiency in the rice-wheat rotation system, being most significant for RCC.

  5. Moessbauer spectroscopic study on inorganic compounds. Pt. 2

    Energy Technology Data Exchange (ETDEWEB)

    Takahashi, Masashi; Kitazawa, Takafumi; Nanba, Hiroshi; Yoshinaga, Tomohiro; Nakajima, Norio; Sumisawa, Yasuhiro; Takeda, Masuo [Toho Univ., Funabashi, Chiba (Japan). Faculty of Science; Sawahata, Hiroyuki; Ito, Yasuo

    1998-01-01

    {sup 166}Er and {sup 127}I Moessbauer spectra were observed. {sup 166}Er Moessbauer spectrum of Er metal and 9 compounds were measured by {sup 166}Ho/Y{sub 0.6}Ho{sub 0.4}H{sub 2} source at 12K and the parameters such as e{sup 2}qQ(mm s{sup -1}), Heff(T) and {tau}(ns) were determined. The relaxation time of ErCl{sub 3}{center_dot}6H{sub 2}O was 0.7ns, long, but that of ErCl{sub 3} was 10 ps, short time. {sup 127}I Moessbauer spectrum of PhI(O{sub 2}CR){sub 2} (R=CH{sub 3}, CHF{sub 2}, CH{sub 2}Cl, CHCl{sub 2}, CCl{sub 3}, CH{sub 2}Br, CHBr{sub 2} and CBr{sub 3}) were observed and compared with that of R`{sub 3}Sb(O{sub 2}CR){sub 2} was similar to that of PhI(O{sub 2}CR){sub 2}. The correlation coefficient between e{sup 2}qQ({sup 127}I) and Mulliken population of carboxylic hydrogen atom of R{sub 2}CO{sub 2}H was -0.87. The relation between the hypervalent bond of O-I-O and that of O-Sb-0 was shown by the equation: e{sup 2}qQ({sup 121}Sb)/mm s{sup -1} = -47.2 + 1.32 e{sup 2}qQ({sup 127}I)/mm s{sup -1}. Hypervalent iodine complex such as (PhI(py){sub 2}){sup 2+} salt and E-Sb-I (E=O, I, N and C) were studied, too. (S.Y.)

  6. Topological Research on Standard Absolute Entropies,S(○)298, for Binary Inorganic Compounds

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    For predicting the standard entropy of a binary inorganic compound, two novel connectivity indexes mQ,mG and their converse indexes mQ',mG' based on adjacency matrix of molecular graphs and ionic parameters gi, qi were pro-posed. The qi and gi are defined as qi=(1.1+Zi1.1)/(1.7+ni), gi:(1.4d-Zi)/(0.9+ri+ri-1), where Zi, ni, ri are the charge numbers, the outer electronic shell primary quantum numbers, and the radii of ionic I respectively. The good Quantitative Structure-Property Relationship (QSPR) models for the standard entropies of binary inorganic com-pound can be constructed from 0Q,0Q',1G, and 1G', by using a multivariate linear regression (MLR) method and an artificial neural network (NN) method. The correlation coefficient r, the standard error s, and the average absolute deviation of the MLR model and the NN model are 0.9905, 8.29 J·K-1,mol-1 and 6.48 J·K-1·mol-1, and 0.9960,5.37 J·K-1·mol-1 and 3.90 J·K-1·mol-1, respectively, for 371 binary inorganic compounds (training set). The cross-validation by using the leave-one-out method demonstrates that the MLR model is highly reliable from the point of view of statistics. The correlation coefficients, standard deviations and average absolute deviations of pre-dicted values of the standard entropies of other 185 binary inorganic compounds (test set) are 0.9897, 8.64 J·K-1·mol-1 and 6.84 J·K-1·mol-1, and 0.9957, 5.63 J·K-1·mol-1 and 4.18 J·K-1·mol-1 for the MLR model and the Nnmodel, respectively. The results show that the current method is more effective than literature methods for estimat-ing the standard entropy of a binary inorganic compound. Both MLR and NN methods can provide acceptable mod-els for the prediction of the standard entropies of binary inorganic compounds. The NN model for the standard en-tropies appears to be more reliable than the MLR model.

  7. Quantitative Structure Property Relations (QSPR) for Predicting Molar Diamagnetic Susceptibilities, χm, of Inorganic Compounds

    Institute of Scientific and Technical Information of China (English)

    MU,Lai-Long; HE,Hong-Mei; FENG,Chang-Jun

    2007-01-01

    For predicting the molar diamagnetic susceptibilities of inorganic compounds, a novel connectivity index mG based on adjacency matrix of molecular graphs and ionic parameter gi was proposed. The gi is defined as gi= (ni0.5-0.91)4·xi0.5/Zi0.5, where Zi, ni, xi are the valence, the outer electronic shell primary quantum number, and the electronegativity of atom I respectively. The good QSPR models for the molar diamagnetic susceptibilities can be constructed from 0G and 1G by using multivariate linear regression (MLR) method and artificial neural network (NN) method. The correlation coefficient r, standard error, and average absolute deviation of the MLR model and NN model are 0.9868, 5.47 cgs, 4.33 cgs, 0.9885, 5.09 cgs and 4.06 cgs, respectively, for the 144 inorganic compounds. The cross-validation by using the leave-one-out method demonstrates that the MLR model is highly reliable from the point of view of statistics. The average absolute deviations of predicted values of the molar diamagnetic susceptibility of other 62 inorganic compounds (test set) are 4.72 cgs and 4.06 cgs for the MLR model and NN model. The results show that the current method is more effective than literature methods for estimating the molar diamagnetic susceptibility of an inorganic compound. Both MLR and NN methods can provide acceptable models for the prediction of the molar diamagnetic susceptibilities. The NN model for the molar diamagnetic susceptibilities appears more reliable than the MLR model.

  8. A golden future in medicinal inorganic chemistry: the promise of anticancer gold organometallic compounds.

    Science.gov (United States)

    Bertrand, Benoît; Casini, Angela

    2014-03-21

    From wedding rings on fingers to stained glass windows, by way of Olympic medals, gold has been highly prized for millennia. Nowadays, organometallic gold compounds occupy an important place in the field of medicinal inorganic chemistry due to their unique chemical properties with respect to gold coordination compounds. In fact, several studies have proved that they can be used to develop highly efficient metal-based drugs with possible applications in the treatment of cancer. This Perspective summarizes the results obtained for different families of bioactive organometallic gold compounds including cyclometallated gold(iii) complexes with C,N-donor ligands, gold(I) and gold(I/III) N-heterocyclic (NHC) carbene complexes, as well as gold(I) alkynyl complexes, with promising anticancer effects. Most importantly, we will focus on recent developments in the field and discuss the potential of this class of organometallic compounds in relation to their versatile chemistry and innovative mechanisms of action.

  9. Influence of Inorganic Ions and Organic Substances on the Degradation of Pharmaceutical Compound in Water Matrix

    Directory of Open Access Journals (Sweden)

    Edyta Kudlek

    2016-11-01

    Full Text Available The paper determined the influence of inorganic substances and high-molecular organic compounds on the decomposition of diclofenac, ibuprofen, and carbamazepine in the process of photocatalysis conducted with the presence of Titanium dioxide (TiO2. It was determined that the presence of such ions as CO 3 2 − , HCO 3 − , HPO 4 2 − as well as SO 4 2 − inhibited the decomposition of carbamazepine, whereas the efficiency of diclofenac degradation was decreased only by the presence of CO 3 2 − and HCO 3 − anions. In case of ibuprofen sodium salt (IBU, all investigated anions influenced the increase in its decomposition rate. The process of pharmaceutical photooxidation conducted in suspensions with Al3+ and Fe3+ cations was characterized by a significantly decreased efficiency when compared to the solution deprived of inorganic compounds. The addition of Ca2+, Mg2+ and NH4+ affected the increase of reaction rate constant value of diclofenac and ibuprofen decomposition. On the other hand, high molecular organic compounds present in the model effluent additionally catalysed the degradation process of pharmaceutical compounds and constituted an additional sorbent that enabled to decrease their concentration. Toxicological analysis conducted in deionized water with pharmaceutical compounds’ patterns proved the production of by-products from oxidation and/or reduction of micropollutants, which was not observed for model effluent irradiation.

  10. Structural Characterization and Infrared and Electrical Properties of the New Inorganic-Organic Hybrid Compound

    Directory of Open Access Journals (Sweden)

    A. Oueslati

    2013-01-01

    Full Text Available New inorganic-organic hybrid [(C3H74N]2Hg2Cl6 compound was obtained and characterised by single-crystal X-ray diffraction, infrared, and impedance spectroscopy. The latter crystallizes in the monoclinic system (space group C 2/c, with the following unit cell dimensions: (1 Å, (6 Å, (2 Å, and (2. Besides, its structure was solved using 84860 independent reflections leading to . Electrical properties of the material were studied using impedance spectroscopic technique at different temperatures in the frequency range of 209 Hz to 5 MHz. Detailed analysis of the impedance spectrum suggested that the electrical properties of the material are strongly temperature-dependent. The Nyquist plots clearly showed the presence of bulk and grain boundary effect in the compound.

  11. The search for organic substances and inorganic volatile compounds in the surface of Mars

    Science.gov (United States)

    Biemann, K.; Oro, J.; Toulmin, P., III; Orgel, L. E.; Nier, A. O.; Anderson, D. M.; Flory, D.; Diaz, A. V.; Rushneck, D. R.; Simmonds, P. G.

    1977-01-01

    A total of four Martian samples, one surface and one subsurface sample at each of the two Viking landing sites, Chryse Planitia and Utopia Planitia, have been analyzed for organic compounds by a gas chromatograph-mass spectrometer. In none of these experiments could organic material of Martian origin be detected at detection limits generally of the order of parts per billion and for a few substances closer to parts per million. The evolution of water and carbon dioxide, but not of other inorganic gases, was observed upon heating the sample to temperatures of up to 500 C. The absence of organic compounds seems to preclude their production on the planet at rates that exceed the rate of their destruction. It also makes it unlikely that living systems that behave in a manner similar to terrestrial biota exist, at least at the two Viking landing sites.

  12. Strain tuning of ferroelectric polarization in hybrid organic inorganic perovskite compounds.

    Science.gov (United States)

    Ghosh, Saurabh; Di Sante, Domenico; Stroppa, Alessandro

    2015-11-19

    Metal-organic frameworks (MOFs) are hybrid crystalline compounds comprised of an extended ordered network made up of organic molecules, organic linkers and metal cations. In particular, MOFs with the same topology as inorganic perovskites have been shown to possess interesting properties, e.g., coexistence of ferroelectric and magnetic ordering. Using first-principles density functional theory, we have investigated the effect of strain on the compounds C(NH2)3Cr(HCOO)3 and (CH3CH2NH3)Mn(HCOO)3. Here, we show that compressive strain can substantially increase the ferroelectric polarization by more than 300%, and we discuss the mechanism involved in the strain enhancement of polarization. Our study highlights the complex interplay between strain and organic cations' dipoles and put forward the possibility of tuning of ferroelectric polarization through appropriate thin film growing.

  13. Performing organic chemistry with inorganic compounds: electrophilic reactivity of selected nitrosyl complexes.

    Science.gov (United States)

    Doctorovich, Fabio; Di Salvo, Florencia

    2007-10-01

    The inorganic nitrosyl (NO(+)) complexes [Fe(CN) 5NO](2-), [Ru(bpy)2(NO)Cl](2+), and [IrCl 5(NO)](-) are useful reagents for the nitrosation of a variety of organic compounds, ranging from amines to the relatively inert alkenes. Regarding [IrCl 5(NO)](-), its high electrophilicity and inertness define it as a unique reagent and provide a powerful synthetic route for the isolation and stabilization of coordinated nitroso compounds that are unstable in free form, such as S-nitrosothiols and primary nitrosamines. Related to the high electrophilicity of [IrCl 5(NO)](-), an unusual behavior is described for its PPh 4(+) salt in the solid state, showing an electronic distribution represented by Ir(IV)-NO(*) instead of Ir (III)-NO(+) (as for the K(+) and Na(+) salts).

  14. 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.

  15. Immunomodulatory effect of selenosemicarbazides and selenium inorganic compounds, distribution in organs after selenium supplementation.

    Science.gov (United States)

    Musik, I; Koziol-Montewka, M; Toś-Luty, S; Pasternak, K; Latuszyńska, J; Tokarska, M; Kielczykowska, M

    1999-12-01

    Antioxidant properties of selenium producing a protective barrier against free radicals play an important role in numerous metabolic and immunologic processes associated with oxidation-reduction reactions which take place during intracellular digestion of phagocyted bacteria. The aim of our study was to examine the properties of an organic compound of selenium, 4-(o-tolilo)-selenosemicarbazide of p-chlorobenzoic acid in terms of its retention in organs, effect on erythropoesis and phagocytic abilities of neutrophiles as well as antioxidant properties in neutrophiles tested with NBT test. This compound as well as inorganic sodium selenate was given to Swiss mice at the dose of 10(-3) g Se/kg for the period of 10 days. The concentrations of selenium in livers of mice treated with sodium selenate and selenosemicarbazide were found to be higher than in controls (18.7 micrograms lg-1 and 23.2 micrograms lg-1 vs. 12 micrograms lg-1, respectively). Analysis of blood cells count has shown a significant decrease in neutrophile levels in both groups treated with selenium. The influence of selenium compounds on phagocytosis and especially NBT test has been determined (3.8% of positive cells in the controls vs. 2.2% and 0.9% in the groups treated with sodium selenate and selenosemicarbazide, respectively). Our preliminary investigations suggest that selenosemicarbazides are biologically active compounds and can modify neutrophile functions.

  16. 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.

  17. Solubility Characteristics and Slow-Release Mechanism of Nitrogen from Organic-Inorganic Compound Coated Urea

    Directory of Open Access Journals (Sweden)

    Hongtao Zou

    2015-01-01

    Full Text Available A soil incubation method was used to investigate the solubility characteristics and slow-release mechanism of organic-inorganic compound coated urea at temperature of 10, 20, and 30°C. The membrane microstructure with and without incubation was tested via scanning electron microscopy (SEM. Slow release of nitrogen (N from different inorganic minerals was analysed by the activation energy from the nutrient solubility system. The rate of nitrogen solubility increased with temperature increasing. The first-order reaction kinetic equation described the solubility process of coated urea. The rate constant k also increased with temperature increasing. Moreover, the SEM images showed that the microstructure of the coating layer changed into a flocculent structure and the number of tiny pores and holes on the membrane surface increased significantly with temperature increasing, which increased N solubility rate. The Arrhenius equation indicated that activation energy was closely related to k during the solubility process; the activation energy was reduced with k rising, which resulted in N solubility rate increasing. Overall, the N solubility rate of coated urea was affected by temperature.

  18. Characterisation of inorganic elements and volatile organic compounds in the dried sea cucumber Stichopus japonicus.

    Science.gov (United States)

    Lee, Hae-Won; Lim, Na-Lae; Cho, Kichul; Yang, Hye Young; Yim, Kyung June; Kim, Mi-Ju; Lee, Myunglip; Kim, Dong Hyeun; Koh, Hyoung Bum; Jung, Won-Kyo; Roh, Seong Woon; Kim, Daekyung

    2014-03-15

    The sea cucumber Stichopus japonicus lives in a variety of marine habitats and is an important cultivated edible aquatic species in East Asia. In this study, S. japonicus, collected from the sea near Jeju Island of Korea, was lyophilised or vacuum-dried and then analysed by gas chromatography-mass spectrometry (GC-MS) or inductively coupled plasma mass spectrometry (ICP-MS). The GC-MS profiles of vacuum-dried and lyophilised samples differed. Based on direct injection and static headspace analysis, 37 volatile organic compounds (VOCs) were identified in vacuum-dried samples and 33 VOCs were identified in lyophilised samples. Therefore, the odour of vacuum-dried sea cucumber is thought to be due to the presence of various VOCs that are absent in lyophilised sea cucumber. According to ICP-MS analysis, the levels of 15 inorganic elements were slightly higher in lyophilised samples than in vacuum-dried samples. The results of the inorganic and organic chemical analyses provide information about the composition of dried sea cucumber. Copyright © 2013 Elsevier Ltd. All rights reserved.

  19. Migration of residual nonvolatile and inorganic compounds from recycled post-consumer PET and HDPE

    Energy Technology Data Exchange (ETDEWEB)

    Dutra, Camila; Reyes, Felix G.R., E-mail: reyesfgr@fea.unicamp.br [Universidade de Campinas (UNICAMP), SP (Brazil). Escola de Engenharia dos Alimentos. Dept. de Ciencias dos Alimentos; Freire, Maria Teresa de A. [Universidade de Sao Paulo (USP), Pirassununga, SP (Brazil). Fac. de Ciencia Animal e Engenharia dos Alimentos. Dept. de Engenharia dos Alimentos; Nerin, Cristina; Bentayeb, Karim; Rodriguez-Lafuente, Angel; Aznar, Margarita [Dept. of Analytical Chemistry, Arago Inst. of Engineering Research, University of Zaragoza (Spain)

    2014-04-15

    Migration of nonvolatile and inorganic residual compounds from post-consumer recycled polyethylene terephthalate (PET) submitted to cleaning processes for subsequent production of materials intended to food contact, as well as from multilayer packaging material containing post-consumer recycled high-density polyethylene (HDPE) was determined. Tests were carried out using food simulant. Nonvolatile organic contaminants from PET, determined by liquid chromatography-mass spectrometry (UPLC-QqQ/MS), showed significant migration reduction as consequence of the more complex cleaning technologies applied. However, contaminants not allowed by Brazilian and European Union regulations were identified even in deep cleaning samples. Results from multilayer HDPE showed a greater number of contaminants when compared to recycled pellets. Inorganic contaminants, determined by inductively coupled plasma mass spectrometry were below the acceptable levels. Additional studies for identification and quantitation of unknown molecules which were not possible to identify in this study by UPLC-QqQ/MS are required to ascertain the safety of using post-consumer recycled packaging material. (author)

  20. Controlling the release of active compounds from the inorganic carrier halloysite

    Science.gov (United States)

    Tescione, F.; Buonocore, G. G.; Stanzione, M.; Oliviero, M.; Lavorgna, M.

    2014-05-01

    Halloysite (HNTs), a natural material characterized by a nanotube structure, has been used as an inorganic carrier of active compounds in several applications from medicine to anticorrosion coatings. In this present work, vanillin (VAN) used as a antimicrobial model, has been encapsulated within HNTs for exploiting its applicability in the active food packaging sector. The molecule release rate has been controlled by crosslinking at the tube ends the loaded vanillin with copper ions, thus producing a stopper network. The vanillin-loaded HNTs were characterized using transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy and thermo gravimetric analysis. The antimicrobial release kinetics from the loaded nanoparticles (VAN/HNTs) in water was investigated using UV-vis spectroscopy. The results show that the vanillin crosslinked with cupper ions is a feasible method to tailor the release rate of antimicrobial model from HTNs nanoparticles.

  1. Controlling the release of active compounds from the inorganic carrier halloysite

    Energy Technology Data Exchange (ETDEWEB)

    Tescione, F.; Buonocore, G. G.; Stanzione, M.; Oliviero, M.; Lavorgna, M. [National Research Council - Institute of Composites and Biomedical Materials, P.le E. Fermi, 1 80055 Portici (Naples) (Italy)

    2014-05-15

    Halloysite (HNTs), a natural material characterized by a nanotube structure, has been used as an inorganic carrier of active compounds in several applications from medicine to anticorrosion coatings. In this present work, vanillin (VAN) used as a antimicrobial model, has been encapsulated within HNTs for exploiting its applicability in the active food packaging sector. The molecule release rate has been controlled by crosslinking at the tube ends the loaded vanillin with copper ions, thus producing a stopper network. The vanillin-loaded HNTs were characterized using transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy and thermo gravimetric analysis. The antimicrobial release kinetics from the loaded nanoparticles (VAN/HNTs) in water was investigated using UV-vis spectroscopy. The results show that the vanillin crosslinked with cupper ions is a feasible method to tailor the release rate of antimicrobial model from HTNs nanoparticles.

  2. Inorganic sulfur-nitrogen compounds: from gunpowder chemistry to the forefront of biological signaling.

    Science.gov (United States)

    Cortese-Krott, Miriam M; Butler, Anthony R; Woollins, J Derek; Feelisch, Martin

    2016-04-14

    The reactions between inorganic sulfur and nitrogen-bearing compounds to form S-N containing species have a long history and, besides assuming importance in industrial synthetic processes, are of relevance to microbial metabolism; waste water treatment; aquatic, soil and atmospheric chemistry; and combustion processes. The recent discovery that hydrogen sulfide and nitric oxide exert often similar, sometimes mutually dependent effects in a variety of biological systems, and that the chemical interaction of these two species leads to formation of S-N compounds brought this chemistry to the attention of physiologists, biochemists and physicians. We here provide a perspective about the potential role of S-N compounds in biological signaling and briefly review their chemical properties and bioactivities in the context of the chronology of their discovery. Studies of the biological role of NO revealed why its chemistry is ideally suited for the tasks Nature has chosen for it; realising how the distinctive properties of sulfur can enrich this bioactivity does much to revive 'die Freude am experimentellen Spiel' of the pioneers in this field.

  3. Bonding in inorganic compounds: a study by x-ray photoelectron spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Avanzino, S.C.

    1978-10-01

    Core electron binding energies were measured for a variety of inorganic and organometallic compounds using gas-phase X-ray photoelectron spectroscopy (XPS). The atomic charge distributions in these molecules are deduced from the binding energies, often leading to a better understanding of the bonding in these compounds. The XPS spectra of fifteen volatile tin compounds were recorded. The data suggest that the metal d orbitals are not significantly involved in the bonding. The oxygen ls XPS spectra of gaseous CH/sub 3/Mn(CO)/sub 5/, (..pi..-C/sub 5/H/sub 5/Fe(CO)/sub 2/)/sub 2/, and Co/sub 4/(CO)/sub 12/ can be readily resolved into separate peaks due to bridging and terminal carbonyl groups. The C ls spectrum of Fe(CO)/sub 5/ consists of a single symmetric peak. The carbonyl ligand core binding energies of transition-metal carbonyl complexes are sensitive to differences in the metal-to-CO ligand bonding. Both C ls and O ls carbonyl binding energies correlate well with average C-O stretching force constants or average C-O stretching frequencies. The metal and carbonyl binding energies in a series of pentacarbonylmanganese complexes LMn(CO)/sub 5/ are a good measure of the relative electronegativities of the ligands L. High-quality X-ray photoelectron spectra have been obtained for compounds dissolved in glycerin solutions, and aqueous solutions were converted into glycerin solutions which gave good XRSspectra of the solutes. The technique appears promising as a future analytical application of X-ray photoelectron spectroscopy. The shifts in the binding energies of oxygen, chlorine, and carbon atoms in some isoelectronic isostructural compounds can be explained in terms of simple trends in atomic charges.

  4. 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.

  5. Simultaneous online monitoring of inorganic compounds in aerosols and gases in an industrialized area

    Science.gov (United States)

    Khezri, Bahareh; Mo, Huan; Yan, Zhen; Chong, Shey-Ling; Heng, Aik Kian; Webster, Richard D.

    2013-12-01

    The automatic MARGA (monitor for aerosols and gases in ambient air) sampling system was used to measure the inorganic ions Cl-, NO3-, SO42-, Na+, NH4+, K+, Mg2+ and Ca2+ in the PM2.5 aerosol phase and the corresponding inorganic gases HCl, HNO2, SO2, HNO3 and NH3 present in the gas phase. Samples were collected and analyzed hourly for 3 months between April and June, 2011, from a sampling site in Singapore close to a heavy industrial area containing extensive petrochemical refineries. The data (hourly and daily average) were analyzed, compared and discussed based on the ratios of HNO2/HNO3 and NH3/NH4+, the levels of nitrate and sulfate, the total nitrogen, the distribution of particulate matter and gaseous compounds, and the acidity of the aerosols. SO2 was the most abundant gas that appeared in an order of magnitude higher concentration than the other trace gases, and correspondingly SO42- was found to be at least 3-10 times higher than other anionic aerosol species. The concentration of major ions in aerosol samples and the related gaseous compounds followed the order of: SO42- > NH4+ > NO3- > K+ > Na+ > Cl- > Ca2+ > Mg2+ and SO2 > NH3 > HNO2 > HNO3, respectively. The maximum values for many of the target analytes occurred during the hazy period in May when there was significant contamination from regional fires. The elevated levels of HNO2 compared to HNO3 and high levels of HNO3 were rationalized based on artifacts in the denuder sampling methodology.

  6. Modeling skills of pre-service chemistry teachers in predicting the structure and properties of inorganic chemistry compounds

    Science.gov (United States)

    Nursa'adah, Euis; Liliasari, Mudzakir, Ahmad

    2016-02-01

    The focus of chemistry is learning about the composition, properties, and transformations of matters. Modeling skills are required to comprehend structure and chemical composition in submicroscopic size. Modeling skills are abilities to produce chemical structure and to explain it into the macroscopic phenomenon and submicroscopic representations. Inorganic chemistry is a study of whole elements in the periodic table and their compounds, except carbon compounds and their derivatives. Knowledge about the structure and properties of chemical substances is a basic model for students in studying inorganic chemistry. Furthermore, students can design and produce to utilize materials needed in their life. This research aimed to describes modeling skills of pre-service chemistry teachers. In order, they are able to determine and synthesize useful materials. The results show that students' modeling skills were in a low level and unable connecting skill categories, even the models of inorganic compounds common. These phenomena indicated that students only describe each element when they learn inorganic chemistry. So that it will make modeling skills of students low. Later, another researches are necessary to develop learning design of inorganic chemistry based on good modeling skills of students.

  7. Electrolytic aminated carbon materials for the electrocatalytic redox reactions of inorganic and organic compounds.

    Science.gov (United States)

    Hayashida, Eriko; Takahashi, Yuichi; Nishi, Hideki; Uchiyama, Shunichi

    2011-06-01

    Some kinds of amine groups can be introduced to the glassy carbon surface by the electrode oxidation of the carbon electrode surface in ammonium carbamate solution, and this amine groups modified electrode is named as an aminated glassy carbon electrode. The existences of not only primary amine but also secondary and tertially amines were confirmed by X ray photoelectron spectroscopy. The applications of the aminated carbon material for the electrocatalytic reductions of oxygen, hydrogen peroxide, and organic compounds such as quinones were carried out, and the effects of amination on the formation of electrocatalytic sites for many species were revealed. The electrocatalyzed cyclic voltammograms of metal ions and metal chelate compounds obtained by aminated glassy carbon electrodes are also discussed. Moreover, we intend to describe that the aminated carbon electrode can exhibit the large reduction waves of inorganic oxoacids such as N02- or bromide ion. The introduced functional groups containing nitrogen atom can change the distribution of the electron densities of the graphite carbon surface, and this specific electron distribution environment may generate the various electrocatalytic activities. Copyright © 2011 The Research Centre for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.

  8. SUPERSPACE-GROUP APPROACH TO THE MODULATED STRUCTURE OF THE INORGANIC MISFIT LAYER COMPOUND (LAS)1.14NBS2

    NARCIS (Netherlands)

    VANSMAALEN, S

    1991-01-01

    The structure of the inorganic misfit layer compound (LaS)1.14NbS2 is reanalysed in the superspace-group formalism, using the recent single-crystal x-ray diffraction data obtained by Meerschaut, Rabu and Rouxel. Structure refinements make it possible to determine the values of the modulation functio

  9. Two New Organo-Inorganic Hybrid Compounds: Nitrilophosphonates of Aluminum and Copper

    Science.gov (United States)

    Cabeza, Aurelio; Bruque, Sebastián; Guagliardi, Antonietta; Aranda, Miguel A. G.

    2001-08-01

    Two new organo-inorganic hybrid compounds, aluminum nitrilotris(methylene)trismonohydrogenphosphonate hydrate, Al[(HO3PCH2)3N]H2O, and tricopper(II) bis-nitrilobis(methylene)diphosphonate, Cu3[(O3PCH2)2NH2]2, have been synthesized. The crystal structures have been determined ab initio from powder diffraction data and refined by the Rietveld method. Al[(HO3PCH2)3N]H2O is monoclinic, space group P21/n, with a=12.1945(3) Å, b=9.1129(3) Å, c=8.5495(2) Å, β=94.317(2)°, Z=4, and the X-ray powder diffraction pattern has been refined to RwP=8.7%. Cu3[(O3PCH2)2NH2]2 is orthorhombic, space group Pbca, with a=16.1209(6) Å, b=9.4890(4) Å, c=9.4113(4) Å, Z=4 and its pattern was refined to RwP=13.5%. The crystal structure of aluminum phosphonate contains a close packing of inorganic chains, formed by alternating AlO6 octahedra and O3PC tetrahedra. These chains are covalently interconnected by the organic groups to give the 3D framework. The structure of copper phosphonate has two distinct copper environments, one a tetragonally elongated tetrahedron and the other a distorted square plane. These structural units are linked by the organic phosphonate. Thermal and infrared data are discussed.

  10. Effects of inorganic and organic arsenic compounds on growth and apoptosis of human T-lymphoblastoid leukemia cells.

    Science.gov (United States)

    Hikita, Eri; Arai, Mariko; Tanaka, Sachiko; Onda, Kenji; Utsumi, Hiroya; Yuan, Bo; Toyoda, Hiroo; Hirano, Toshihiko

    2011-12-01

    To investigate the effects of inorganic and organic arsenic compounds on human T-lymphoblastoid leukemia cells. Cell proliferation was analyzed by 3-(4,5-dimethylthiazol-2-yl)-2,5¬diphenyltetrazolium bromide (MTT) assay. Apoptotic cell morphology was examined by cell staining with Hoechst 33342. Cellular caspase-3/7 activities were measured after arsenic treatment. The inhibitory concentration by 50% (IC(50)) values of As(2)O(3) towards MOLT-4 and daunorubicin- resistant MOLT-4/DNR cell proliferation were 0.87 and 0.92 μM, while the values for arsenic acid were 69.1 and 116.6 μM, respectively. These arsenic compounds also inhibited mitogen-induced proliferation of human peripheral blood mononuclear cells. Six organic arsenic compounds did not inhibit leukemia cell proliferation. As(2)O(3) and arsenic acid induced apoptotic cell morphology and increased caspase-3/7 activity in the leukemia cells. Ascorbic acid and buthionine sulfoxide enhanced, while N-acetyl-L-cysteine abated, the suppressive effects of inorganic arsenic compounds on leukemia cell proliferation. As(2)O(3) and arsenic acid inhibit proliferation and induce apoptosis in MOLT-4 and daunorubicine-resistant MOLT-4/DNR cells via glutathione-depletion and subsequent caspase-3/7 activation. Organic arsenic compounds have no inhibitory activity on the leukemia cell proliferation. Inorganic arsenic compounds are suggested as useful agents for treatment of T-lymphoblastoid leukemia.

  11. The Production of Organic-Inorganic Compound Film-Coated Urea and the Characteristics of Its Nutrient Release

    Institute of Scientific and Technical Information of China (English)

    ZOU Hong-tao; WANG Yao-sheng; SONG Hao-wen; HAN Yan-yu; YU Na; ZHANG Yu-ling; DANG Xiu-li; HUANG Yi; ZHANG Yu-long

    2009-01-01

    The effect of different concentrations of natural macromolecular compound on the characteristics of nutrient release in the membrane materials of organic-inorganic compound film-coated urea was discussed,and the optimal concentrations for better nutrient release was proposed.The characteristics of nutrient release of film-coated urea were evaluated by soil column leaching experiment.Organic-inorganic compound film-coated urea showed good characteristics of nutrient release,which could be well simulated by Logistic curve.The two parameters in this curve,a and r,can be used to present nutrient release of film-coated urea,and followed the order of B > C > A and C < B < A,respectively,indicating that the release was stronger with the increasing concentration of natural maeromolecular compound in the membrane,which implied better controllability of nutrient release.The concentration of 5% of natural macromolecular compound showed better characteristic of nutrient release and can be utilized as a membrane material combined with inorganic mineral powders to develop film-coated slow-release fertilizer.

  12. Toward design of multiple-property inorganic-organic hybrid compounds based on face-sharing octahedral iodoplumbate chains.

    Science.gov (United States)

    Zhao, Shun-Ping; Ren, Xiao-Ming

    2011-09-07

    In this review article, we have illustrated the strategies developed to achieve inorganic-organic hybrid compounds with technologically important physical properties. A series of target inorganic-organic hybrid compounds have been accomplished by incorporating the functional organic components (with a large hyperpolarizability and luminophore Schiff base cation) into the highly polarizable one-dimensional (1-D) iodoplumbate chain network. The effect of substituent features in the phenyl ring of the Schiff base cation on its molecular conformation as well as the crystal packing structure of the hybrid compound will be discussed and the multiple physical properties (ferroelectricity, NLO and multiple band emission) will also be mentioned. This journal is © The Royal Society of Chemistry 2011

  13. Simultaneous determination of inorganic mercury and methylmercury compounds in natural waters

    Energy Technology Data Exchange (ETDEWEB)

    Logar, Martina; Horvat, Milena [Jozef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia); Akagi, Hirokatsu [National Institute for Minamata Disease, 4058-18 Hama, Minamata, Kumamoto 867-0008 (Japan); Pihlar, Boris [Faculty of Chemistry and Chemical Technology, University of Ljubljana, Askerceva 5, 1000 Ljubljana (Slovenia)

    2002-11-01

    The purpose of the present work was to develop a simple, rapid, sensitive and accurate method for the simultaneous determination of inorganic mercury (Hg{sup 2+}) and monomethylmercury compounds (MeHg) in natural water samples at the pg L{sup -1} level. The method is based on the simultaneous extraction of MeHg and Hg{sup 2+}dithizonates into an organic solvent (toluene) after acidification of about 300 mL of a water sample, followed by back extraction into an aqueous solution of Na {sub 2}S, removal of H {sub 2}S by purging with N {sub 2}, subsequent ethylation with sodium tetraethylborate, room temperature precollection on Tenax, isothermal gas chromatographic separation (GC), pyrolysis and cold vapour atomic fluorescence spectrometric detection (CV AFS) of mercury. The limit of detection calculated on the basis of three times the standard deviation of the blank was about 0.006 ng L {sup -1} for MeHg and 0.06 ng L {sup -1} for Hg {sup 2+}when 300 mL of water was analysed. The repeatability of the results was about 5% for MeHg and 10% for Hg {sup 2+}. Recoveries were 90-110% for both species. (orig.)

  14. Atmospheric Deposition of Inorganic Elements and Organic Compounds at the Inlets of the Venice Lagoon

    Directory of Open Access Journals (Sweden)

    E. Morabito

    2014-01-01

    Full Text Available The Venice Lagoon is subjected to long-range transport of contaminants via aerosol from the near Po Valley. Moreover, it is an area with significant local anthropogenic emissions due to the industrial area of Porto Marghera, the urban centres, and the glass factories and with emissions by ships traffic within the Lagoon. Furthermore, since 2005, the Lagoon has also been affected by the construction of the MOSE (Modulo Sperimentale Elettromeccanico—Electromechanical Experimental Module mobile dams, as a barrier against the high tide. This work presents and discusses the results from chemical analyses of bulk depositions, carried out in different sites of the Venice Lagoon. Fluxes of pollutants were also statistically analysed on PCA with the aim of investigating the spatial variability of depositions and their correlation with precipitations. Fluxes of inorganic pollutants depend differently on precipitations, while organic compounds show a more seasonal trend. The statistical analysis showed that the site in the northern Lagoon has lower and almost homogeneous fluxes of pollutants, while the other sites registered more variable concentrations. The study also provided important information about the annual trend of pollutants and their evolution over a period of about five years, from 2005 to 2010.

  15. Simultaneous removal of inorganic and organic compounds in wastewater by freshwater green microalgae.

    Science.gov (United States)

    Zhou, Guang-Jie; Ying, Guang-Guo; Liu, Shan; Zhou, Li-Jun; Chen, Zhi-Feng; Peng, Fu-Qiang

    2014-08-01

    Batch experiments were carried out for 7 days to investigate the simultaneous removal of various organic and inorganic contaminants including total nitrogen (TN), total phosphorus (TP), metals, pharmaceuticals and personal care products (PPCPs), endocrine disrupting chemicals (EDCs), and estrogenic activity in wastewater by four freshwater green microalgae species, Chlamydomonas reinhardtii, Scenedesmus obliquus, Chlorella pyrenoidosa and Chlorella vulgaris. After treatment for 7 days, 76.7-92.3% of TN, and 67.5-82.2% of TP were removed by these four algae species. The removal of metals from wastewater by the four algae species varied among the metal species. These four algae species could remove most of the metals efficiently (>40% removal), but showed low efficiencies in removing Pb, Ni and Co. The four algae species were also found to be efficient in removing most of the selected organic compounds with >50% removal, and the estrogenic activity with removal efficiencies ranging from 46.2 to 81.1% from the wastewater. Therefore, algae could be harnessed to simultaneously remove various contaminants in wastewater.

  16. Stoichiometric modeling of oxidation of reduced inorganic sulfur compounds (Riscs) in Acidithiobacillus thiooxidans.

    Science.gov (United States)

    Bobadilla Fazzini, Roberto A; Cortés, Maria Paz; Padilla, Leandro; Maturana, Daniel; Budinich, Marko; Maass, Alejandro; Parada, Pilar

    2013-08-01

    The prokaryotic oxidation of reduced inorganic sulfur compounds (RISCs) is a topic of utmost importance from a biogeochemical and industrial perspective. Despite sulfur oxidizing bacterial activity is largely known, no quantitative approaches to biological RISCs oxidation have been made, gathering all the complex abiotic and enzymatic stoichiometry involved. Even though in the case of neutrophilic bacteria such as Paracoccus and Beggiatoa species the RISCs oxidation systems are well described, there is a lack of knowledge for acidophilic microorganisms. Here, we present the first experimentally validated stoichiometric model able to assess RISCs oxidation quantitatively in Acidithiobacillus thiooxidans (strain DSM 17318), the archetype of the sulfur oxidizing acidophilic chemolithoautotrophs. This model was built based on literature and genomic analysis, considering a widespread mix of formerly proposed RISCs oxidation models combined and evaluated experimentally. Thiosulfate partial oxidation by the Sox system (SoxABXYZ) was placed as central step of sulfur oxidation model, along with abiotic reactions. This model was coupled with a detailed stoichiometry of biomass production, providing accurate bacterial growth predictions. In silico deletion/inactivation highlights the role of sulfur dioxygenase as the main catalyzer and a moderate function of tetrathionate hydrolase in elemental sulfur catabolism, demonstrating that this model constitutes an advanced instrument for the optimization of At. thiooxidans biomass production with potential use in biohydrometallurgical and environmental applications.

  17. STUDY ON POLYMERIC CATALYST—PALLADIUM COMPLEX WITH RADIATION GRAFTING ACRYLONITRILE ON INORGANIC COMPOUND

    Institute of Scientific and Technical Information of China (English)

    ZHANGWanxi; CHEJitai

    1993-01-01

    Polymer bound palladium (Pd) complex catalysts with grafting acrylonitrile on inorganic compound(MgO,Y-molecular sieve and SiO2) by pre-radiation method were studies.The palladium-grafting polymers have been investigated by X-ray photoelectron spectrscopy(XPS).It is indicated that peak width of C1s and O1s spectra of MgO-g-PAN-Pd(radiation-induced graft) is wider than that of MgO-PAN-Pd(chemical method) and Peak numbers of former are one more than later.According to the report in reference,this peak is attributed to -O-C group.Thus,the graft acrylonitrile on MgO may complete through oxygen atoms im MgO and β-carbon atoms in acrylonitrile.The polymer catalyst obtained by radiation grafting is a higher active hydrogenation catalyst for olefines and better antioxic than that of one obtained by chemical method,and it has selectivity for hydrogenation catalyst.

  18. Reactions of chlorine with inorganic and organic compounds during water treatment-Kinetics and mechanisms: a critical review.

    Science.gov (United States)

    Deborde, Marie; von Gunten, Urs

    2008-01-01

    Numerous inorganic and organic micropollutants can undergo reactions with chlorine. However, for certain compounds, the expected chlorine reactivity is low and only small modifications in the parent compound's structure are expected under typical water treatment conditions. To better understand/predict chlorine reactions with micropollutants, the kinetic and mechanistic information on chlorine reactivity available in literature was critically reviewed. For most micropollutants, HOCl is the major reactive chlorine species during chlorination processes. In the case of inorganic compounds, a fast reaction of ammonia, halides (Br(-) and I(-)), SO(3)(2-), CN(-), NO(2)(-), As(III) and Fe(II) with HOCl is reported (10(3)-10(9)M(-1)s(-1)) whereas low chlorine reaction rates with Mn(II) were shown in homogeneous systems. Chlorine reactivity usually results from an initial electrophilic attack of HOCl on inorganic compounds. In the case of organic compounds, second-order rate constants for chlorination vary over 10 orders of magnitude (i.e. organic compounds are possible pathways. However, from a kinetic point of view, usually only electrophilic attack is significant. Chlorine reactivity limited to particular sites (mainly amines, reduced sulfur moieties or activated aromatic systems) is commonly observed during chlorination processes and small modifications in the parent compound's structure are expected for the primary attack. Linear structure-activity relationships can be used to make predictions/estimates of the reactivity of functional groups based on structural analogy. Furthermore, comparison of chlorine to ozone reactivity towards aromatic compounds (electrophilic attack) shows a good correlation, with chlorine rate constants being about four orders of magnitude smaller than those for ozone.

  19. Mechanism of oxidation of inorganic sulfur compounds by thiosulfate-grown Thiobacillus thiooxidans.

    Science.gov (United States)

    Masau, R J; Oh, J K; Suzuki, I

    2001-04-01

    Thiobacillus thiooxidans was grown at pH 5 on thiosulfate as an energy source, and the mechanism of oxidation of inorganic sulfur compounds was studied by the effect of inhibitors, stoichiometries of oxygen consumption and sulfur, sulfite, or tetrathionate accumulation, and cytochrome reduction by substrates. Both intact cells and cell-free extracts were used in the study. The results are consistent with the pathway with sulfur and sulfite as the key intermediates. Thiosulfate was oxidized after cleavage to sulfur and sulfite as intermediates at pH 5, the optimal growth pH on thiosulfate, but after initial condensation to tetrathionate at pH 2.3 where the organism failed to grow. N-Ethylmaleimide (NEM) inhibited sulfur oxidation directly and the oxidation of thiosulfate or tetrathionate indirectly. It did not inhibit the sulfite oxidation by cells, but inhibited any reduction of cell cytochromes by sulfur, thiosulfate, tetrathionate, and sulfite. NEM probably binds sulfhydryl groups, which are possibly essential in supplying electrons to initiate sulfur oxidation. 2-Heptyl-4-hydroxy-quinoline N-oxide (HQNO) inhibited the oxidation of sulfite directly and that of sulfur, thiosulfate, and tetrathionate indirectly. Uncouplers, carbonyl cyanide-m-chlorophenylhydrazone (CCCP) and 2,4-dinitrophenol (DNP), inhibited sulfite oxidation by cells, but not the oxidation by extracts, while HQNO inhibited both. It is proposed that HQNO inhibits the oxidation of sulfite at the cytochrome b site both in cells and extracts, but uncouplers inhibit the oxidation in cells only by collapsing the energized state of cells, delta muH+, required either for electron transfer from cytochrome c to b or for sulfite binding.

  20. Comparison of organic and inorganic germanium compounds in cellular radiosensitivity and preparation of germanium nanoparticles as a radiosensitizer.

    Science.gov (United States)

    Lin, Ming-Hsing; Hsu, Tzu-Sheng; Yang, Pei-Ming; Tsai, Meng-Yen; Perng, Tsong-Pyng; Lin, Lih-Yuan

    2009-03-01

    The aim of this work is to compare the radiosensitizing effect between organic and inorganic germanium compounds and to investigate whether nanometer-sized germanium particles can act as radiosensitizers. Bis (2-carboxyethylgermanium) sesquioxide (Ge-132), germanium oxide (GeO(2)) and germanium nanoparticles were used in this study. Cell viability was determined by clonogenic survival assay. Cellular DNA damage was evaluated by alkaline comet assay, confocal microscopy and the cellular level of phospho-histone H2AX (gamma-H2AX). Nanometer-sized germanium particles were fabricated. They have a similar radiosensitizing effect as that of GeO(2). Conversely, Ge-132 did not enhance the radiosensitivity of cells. Comet assay was employed to evaluate the level of DNA damage and confirmed that inorganic germanium compounds enhanced cellular radiosensitivity. Notably, the comet assay indicated that the nanoparticle itself caused a higher level of DNA damage. The possibility that germanium nanoparticles per se caused DNA damage was ruled out when the cellular level of gamma-H2AX was examined. We demonstrated that inorganic but not organic germanium compounds exerted radiosensitizing effect in cells. Nanometer-sized germanium particles were fabricated and were able to enhance the radiosensitivity of cells. Confounding effect may occur when comet assay is used to estimate the level of DNA damage in the presence of germanium nanoparticles.

  1. 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.

  2. High performance organic-inorganic perovskite-optocoupler based on low-voltage and fast response perovskite compound photodetector

    Science.gov (United States)

    Li, Dong; Dong, Guifang; Li, Wenzhe; Wang, Liduo

    2015-01-01

    Organic-inorganic hybrid photodetectors attract considerable attention because they can combine the advantages of both organic and inorganic systems. Here, a perovskite compound with a broad absorption spectrum and high power conversion efficiency is used as a photosensitive layer in an organic/inorganic hybrid heterojunction photodetector with a high and fast response. The high sensitivity exceeding 104 is obtained at bias of 0–4 V. Using a tandem organic light-emitting diode (OLED) as the light source, we fabricated an optocoupler device. The optocoupler achieved a maximum photoresponsivity of 1.0 A W−1 at 341.3 μWcm−2 at an input voltage of 6 V. The device also exhibits rapid response times of τrise ~ 20 μs and τfall ~ 17 μs; as well as a high current transfer ratio (CTR) of 28.2%. After applying an amplification circuit, the CTR of the optocoupler increases to 263.3%, which is comparable with that of commercial inorganic optocouplers. The developed hybrid optocoupler thus shows great promise for use in photonics. PMID:25600830

  3. Contribution and distribution of inorganic ions and organic compounds to the osmotic adjustment in Halostachys caspica response to salt stress.

    Science.gov (United States)

    Zeng, Youling; Li, Ling; Yang, Ruirui; Yi, Xiaoya; Zhang, Baohong

    2015-09-09

    The mechanism by which plants cope with salt stress remains poorly understood. The goal of this study is to systematically investigate the contribution and distribution of inorganic ions and organic compounds to the osmotic adjustment (OA) in the halophyte species Halostachys caspica. The results indicate that 100-200 mM NaCl is optimal for plant growth; the water content and degree of succulence of the assimilating branches are higher in this treatment range than that in other treatments; parenchyma cells are more numerous with 100 mM NaCl treatment than they are in control. Inorganic ions (mainly Na+ and Cl-) may play a more important role than organic compounds in NaCl-induced OA and are the primary contributors in OA in H. caspica. The inorganic ions and organic solutes display a tissue-dependent distribution. Na+ and Cl- are accumulated in the reproductive organs and within assimilating branches, which may represent a mechanism for protecting plant growth by way of salt ion dilution and organ abscission. Additionally, OA via increased accumulation of organic substances also protected plant growth and development. This finding provides additional evidence for plant tolerance to salinity stress which can be used for breeding new cultivars for stress tolerance.

  4. The observation of scintillation in a hydrated inorganic compound: CeCl3 6H2O

    Energy Technology Data Exchange (ETDEWEB)

    Boatner, Lynn A [ORNL; Neal, John S [ORNL; Ramey, Joanne Oxendine [ORNL; Chakoumakos, Bryan C [ORNL; Custelcean, Radu [ORNL

    2013-01-01

    We have recently reported the discovery of a new family of rare-earth metal-organic single-crystal scintillators based on Ce3+ as the activator ion. Starting with the CeCl3(CH3OH)4 prototype, this family of scintillators has recently been extended to include complex metal-organic adducts produced by reacting CeCl3 with heavier organics (e.g., isomers of propanol and butanol). Some of these new rare-earth metal-organic materials incorporated waters of hydration in their structures, and the observation of scintillation in these hydrated compounds was an original finding for any solid scintillator. In the present work, we now report what is apparently the initial observation of gamma-ray-excited scintillation in an inorganic hydrated material, namely single-crystal monoclinic CeCl3 6H2O. This observation shows that the mechanisms of the various scintillation energy-transfer processes are not blocked by the presence of waters of hydration in an inorganic material and that the observation of scintillation in other hydrated inorganic compounds is not precluded.

  5. A Statistical Learning Framework for Materials Science: Application to Elastic Moduli of k-nary Inorganic Polycrystalline Compounds

    Science.gov (United States)

    de Jong, Maarten; Chen, Wei; Notestine, Randy; Persson, Kristin; Ceder, Gerbrand; Jain, Anubhav; Asta, Mark; Gamst, Anthony

    2016-01-01

    Materials scientists increasingly employ machine or statistical learning (SL) techniques to accelerate materials discovery and design. Such pursuits benefit from pooling training data across, and thus being able to generalize predictions over, k-nary compounds of diverse chemistries and structures. This work presents a SL framework that addresses challenges in materials science applications, where datasets are diverse but of modest size, and extreme values are often of interest. Our advances include the application of power or Hölder means to construct descriptors that generalize over chemistry and crystal structure, and the incorporation of multivariate local regression within a gradient boosting framework. The approach is demonstrated by developing SL models to predict bulk and shear moduli (K and G, respectively) for polycrystalline inorganic compounds, using 1,940 compounds from a growing database of calculated elastic moduli for metals, semiconductors and insulators. The usefulness of the models is illustrated by screening for superhard materials. PMID:27694824

  6. A Statistical Learning Framework for Materials Science: Application to Elastic Moduli of k-nary Inorganic Polycrystalline Compounds

    Science.gov (United States)

    de Jong, Maarten; Chen, Wei; Notestine, Randy; Persson, Kristin; Ceder, Gerbrand; Jain, Anubhav; Asta, Mark; Gamst, Anthony

    2016-10-01

    Materials scientists increasingly employ machine or statistical learning (SL) techniques to accelerate materials discovery and design. Such pursuits benefit from pooling training data across, and thus being able to generalize predictions over, k-nary compounds of diverse chemistries and structures. This work presents a SL framework that addresses challenges in materials science applications, where datasets are diverse but of modest size, and extreme values are often of interest. Our advances include the application of power or Hölder means to construct descriptors that generalize over chemistry and crystal structure, and the incorporation of multivariate local regression within a gradient boosting framework. The approach is demonstrated by developing SL models to predict bulk and shear moduli (K and G, respectively) for polycrystalline inorganic compounds, using 1,940 compounds from a growing database of calculated elastic moduli for metals, semiconductors and insulators. The usefulness of the models is illustrated by screening for superhard materials.

  7. Profiling of soil volatile organic compounds after long-term application of inorganic, organic and organic-inorganic mixed fertilizers and their effect on plant growth.

    Science.gov (United States)

    Raza, Waseem; Mei, Xinlan; Wei, Zhong; Ling, Ning; Yuan, Jun; Wang, Jichen; Huang, Qiwei; Shen, Qirong

    2017-12-31

    The complexity of soil processes involved in the production, consumption and accumulation of volatile organic compounds (VOCs) makes hard to access the overall dynamics of VOCs in the soil. In this study, the field soil, applied with inorganic (CF), organic (OF) and inorganic-organic mixed (CFOF) fertilizers for ten years was evaluated for the emission of VOCs at different temperature and moisture levels. We identified 30-50 soil emitted VOCs representing the most common soil VOCs groups by using the solid-phase microextraction (SPME) fiber and gas chromatography-mass spectroscopy. The highest total emission of VOCs was found in OF treatment, but it was non-significantly different with CF treatment. The emission of VOCs was significantly increased with the decrease in moisture contents and increase in the temperature of the soil. Among different fertilizer treatments, the emission of VOCs was significantly higher in OF treatment at 5% moisture, and in CF and OF treatments at 35°C. Further, the VOCs emitted from soil treated with CFOF showed the highest increase in plant growth while CF and OF treatments showed similar results. The VOCs were also extracted from the soil using methanol to better understand the dynamics of VOCs. The abundance of VOCs extracted from the soil was 44-61%, while the richness was 65-70% higher than the VOCs emitted from the soil in different treatments. Taken together the results of emitted and extracted VOCs from the soil, we conclude that the fertilizers are able to discriminate among the VOC patterns of soil. In addition, most of the VOCs are retained in the soil and the emission of VOCs from soil depends on the type of VOCs, soil properties and environmental conditions; however, more research is required to find out better soil VOCs analysis methods. Copyright © 2017. Published by Elsevier B.V.

  8. Inorganic compounds and materials as catalysts for oxidations with aqueous hydrogen peroxide

    NARCIS (Netherlands)

    Nardello, veronique; Aubry, Jean-Marie; De Vos, Dirk E.; Neumann, Ronny; Adam, Waldemar; Zhang, Rui; ten Elshof, Johan E.; Witte, Peter T.; Alsters, Paul L.

    2006-01-01

    This paper reviews our work on oxidations with aqueous hydrogen peroxide catalyzed by inorganic catalysts devoid of organic ligands. In the first part of the review, the use of the [WZn3(ZnW9O34)2]12− “sandwich” polyoxometalate as a multi-purpose oxidation catalyst is described. Attention is paid to

  9. Inorganic compounds and materials as catalysts for oxidations with aqueous hydrogen peroxide

    NARCIS (Netherlands)

    Nardello, veronique; Aubry, Jean-Marie; Vos, De Dirk E.; Neumann, Ronny; Adam, Waldemar; Zhang, Rui; Elshof, ten Johan E.; Witte, Peter T.; Alsters, Paul L.

    2006-01-01

    This paper reviews our work on oxidations with aqueous hydrogen peroxide catalyzed by inorganic catalysts devoid of organic ligands. In the first part of the review, the use of the [WZn3(ZnW9O34)2]12− “sandwich” polyoxometalate as a multi-purpose oxidation catalyst is described. Attention is paid to

  10. Study on the Built-up Effect of Inorganic Compounds to Flame Retardant Containing Organophosphorus in Suppression of Smoke

    Institute of Scientific and Technical Information of China (English)

    LIN Miao; XIAN Chun-ying; YANG Yong

    2006-01-01

    The built-up effect of inorganic compounds containing more active metal ions, such as Ca2+ , Al3+ , Cu2+ , and Zn2+ , as additives adding to phosphorus-containing flame retarding systems in suppression of smoke was studied. The data presented herein suggested that the amount of smoke in the burning process can be better suppressed after the cotton fabric finishing with built- up system was burnt. Some general principles were identified, and the likely causes of the observed effects were analyzed according to test data.

  11. A curved multi-component aerosol hygroscopicity model framework: Part 1 – Inorganic compounds

    Directory of Open Access Journals (Sweden)

    D. O. Topping

    2005-01-01

    Full Text Available A thermodynamic modelling framework to predict the equilibrium behaviour of mixed inorganic salt aerosols is developed, and then coupled with a technique for finding a solution to the Kohler equation in order to create a diameter dependent hygroscopic aerosol model (Aerosol Diameter Dependent Equilibrium Model – ADDEM. The model described here provides a robust and accurate inorganic basis using a mole fraction based activity coefficient model and adjusted energies of formation for treating solid precipitation. The model framework can accommodate organic components, though this added complexity is considered in a companion paper, this paper describes the development of the modelling architecture to be used and predictions of an inorganic model alone. The modelling framework has been developed to flexibly use a combination of mixing rules and other potentially more accurate techniques where available to calculate the water content. Comparisons with other state-of-the-art general equilibrium models and experimental data are presented and show excellent agreement. The Kelvin effect can be considered in this scheme using a variety of surface tension models. Comparison of predicted diameter dependent phenomena, such as the increased relative humidity for onset of deliquescence with decreasing diameter, with another diameter dependent model is very good despite the different approach used. The model is subject to various sensitivities. For the inorganic systems studied here, the model is sensitive to choice of surface tension scheme used, which decreases for larger aerosol. Large sensitivities are found for the value of dry density used. It is thus likely that the history of the aerosol studied in a hygroscopic tandem differential mobility analyser (HTDMA, specifically the nature of the drying process that will influence the final crystalline form, will create systematic uncertainties upon comparisons with theoretical predictions. However, the

  12. Effects of an inorganic and two new organic compounds of selenium on morphologic blood elements and antioxidant status in mice.

    Science.gov (United States)

    Musik, Irena; Kozioł-Montewka, Maria; Pasternak, Kazimierz; Toś-Luty, Sabina; Tokarska, Małgorzata

    2003-01-01

    Two organic compounds, 4-(o-tolilo-)-selenosemicarbazide of p-chlorobenzoic acid and 3-(p-chlorobenzoylamino-)-2-(o-tolylimino-)-4-phenyl-4-selenazoline were compared to the effects of the supplementation with inorganic Na2SeO3. Studies were carried out in four groups consisting of 10 female mice each of SWISS strain. Three of them were supplemented with different selenium formula at the dose of 10(-3) mg Se per g over the period of 10 day. The blood samples were collected to heparinized test tubes; the red blood and white blood count, hematocrit and haemoglobin concentration were studied. The influence of selenium compounds on phagocytosis and NBT test was determined.

  13. 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.)

  14. New organic-inorganic hybrid compounds constructed from polyoxometalates and transition metal mixed-organic-ligand complexes.

    Science.gov (United States)

    Hu, Yang-Yang; Zhang, Ting-Ting; Zhang, Xiao; Zhao, De-Chuan; Cui, Xiao-Bing; Huo, Qi-Sheng; Xu, Ji-Qing

    2016-02-14

    Five new organic-inorganic hybrid compounds based on different polyoxoanions [HxGeW12O40](n-) or [H3As2W18O62](3-) (x = 0, 2; n = 4, 2), namely [Cu3(2,2'-bpy)3(inic)(OH)(H2O)][GeW12O40]·1.5H2O (1), [Cu2(phen)2(μ2-Cl)2(inic)]2[H2GeW12O40]·2H2O (2), [Cu2(phen)2(μ2-Cl)Cl(nic)]2[H2GeW12O40] (3), [Cu2(2,2'-bpy)2(hnic)Cl]2[H2GeW12O40] (4), [Cu(phen)(inic)H2O][Cu2(phen)2(inic)2(H2O)][H3As2W18O62]·3H2O (5) (inic = isonicotinic acid, nic = nicotinic acid, hnic = 2-hydroxy-nicotinic acid, 2,2'-bpy = 2,2'-bipyridine, phen = 1,10-phenanthroline), have been synthesized and characterized by IR, UV-Vis, XRD, cyclic voltammetric measurements and single crystal X-ray diffraction analysis. Single crystal X-ray analysis reveals that compound 1 is isomorphous and isostructural with a compound reported by us recently, the main difference between the two is the heteroatom of the polyoxoanions in the two compounds. Compound 2 is a supramolecular structure constructed from polyoxoanions and transition metal mixed-organic-ligand complexes. Compound 3 is a novel polyoxoanion bi-supported transition metal mixed-organic-ligand complex. Compound 4 is a 1-D chain structure constructed from polyoxoanions and transition metal mixed-organic-ligand complexes. The photodegradation properties of compounds 1-5 have been analyzed.

  15. A review on how Lanthanide impurity levels change with chemistry and structure of inorganic compounds

    NARCIS (Netherlands)

    Dorenbos, P.

    2012-01-01

    The energy of the 4f-5d transitions of divalent and trivalent lanthanide impurities in compounds depends strongly on the type of lanthanide, its valence, and the type of compound. Despite this large variability there is much systematic in 4f-5d transition energy. Once it is known for one lanthanide

  16. Synthesis, crystal structure and electrical properties of the new organic-inorganic hybrid compound bis(1-chlorido-4-aminopyridinium) octachlorodiantimoinate

    Science.gov (United States)

    Fersi, Mohamed Amine; Hajji, Rachid; Chaabane, Iskandar; Gargouri, Mohamed

    2017-10-01

    Bis(1-chlorido-4-aminopyridinium) octachlorodiantimoinate has been synthesized and characterized by a single-crystal X-ray diffraction at 296 K and impedance spectroscopy. At room temperature, the title compound is crystallized in the triclinic system (P 1 ̅ space group) with Z = 2 and the following unit cell dimensions: a = 7.919 (1) Å, b = 9.624 (1) Å, c = 17.692 (3) Å, α = 101.81 (1)°, β = 95.12 (1)°and γ = 112.48 (1)°. The crystal structure of the [C10H12Cl2N4]Sb2Cl8 compound is built of two un-equivalent monoprotonated cations [C5H6N2Cl] + and two un-equivalent tetrachloroantimonate (III) anions noted which are [Sb(1)Cl4]- and [Sb(2)Cl4]-. The arrangement of this compound can be described by an alternation of organic and inorganic layers stacked along [010] direction. The cohesion of compound entities is ensured by hydrogen bonding (N-H…. Cl) and Van Der Waals interaction (C-H…. Cl). The temperature dependence of the σdc conductivity exhibits an Arrhenius type behavior described by the following expression σdc T = Aexp(-Ea/kβT). The Ac conductivity and the dielectric loss suggest that the correlated barrier hopping is the appropriate model for the conduction mechanism.

  17. Antiproliferative and anti-invasive effects of inorganic and organic arsenic compounds on human and murine melanoma cells in vitro.

    Science.gov (United States)

    Hiwatashi, Yoko; Tadokoro, Hiroko; Henmi, Kayo; Arai, Mariko; Kaise, Toshikazu; Tanaka, Sachiko; Hirano, Toshihiko

    2011-09-01

    For patients with advanced melanoma, no treatment options are available at present that provide either sufficient response rates or a significant prolongation of overall survival. The present study examines the effects of two inorganic and six organic arsenic compounds on cell proliferation and cell invasion of melanoma cells in vitro. The effects of arsenic compounds on proliferation of human melanoma A375 cells and murine melanoma B16F10 cells were examined by MTT assay and 5-bromo-2'-deoxyuridine (BrdU) incorporation assay, and the effects of the compounds on cell invasion were examined by the Boyden chamber invasion assay. The amounts of active matrix metalloproteinase (MMP)-2 and pro-MMP-2 in the culture supernatant of A375 cells were determined by an MMP-2 activity assay system. Arsenate and arsenic trioxide (As(2) O(3) ) inhibited the proliferation of A375 and B16F10 cells significantly at concentration ranges of 0.1-20µg/ml (Porganic compounds arsenobetaine, arsenocholine, dimethylarsinic acid, methylarsonic acid, tetramethylarsonium and trimethylarsine oxide did not show any inhibitory effects even at 20µg/ml. Cell invasion of A375 and B16F10 cells through a layer of collagen IV was significantly inhibited by 0.1-20 µg/ml of arsenate or As(2) O(3) (Porganic compounds did not inhibit cell invasion. Arsenate or As(2) O(3) at 0.2-10µg/ml significantly inhibited the amount of active MMP-2 and pro-MMP-2 secreted into the A375 cell culture supernatant (Pinorganic arsenic compounds arsenate and As(2) O(3) inhibit cell proliferation and prevent the invasive properties of melanoma cells, possibly by decreasing MMP-2 production from the cells. © 2011 The Authors. JPP © 2011 Royal Pharmaceutical Society.

  18. Influence of lead Inorganic Compounds on Combustion Rate of Double Base Rocket Propellants

    Directory of Open Access Journals (Sweden)

    V. B. Pillai

    1982-04-01

    Full Text Available The influence of lead nitrate, red lead, lead chromate, lead floride and lead carbonate on the combustion behaviour of double base propellants in the pressure range-35-140kg/cm /sup 2/ was studied. While all these compounds increased burning rates in lower pressure range (35-60 kg/cm/sup 2/ and higher pressure range (120-140 kg/cm/sup 2/, only lead chromate and lead fluoride were effective in the intermediate pressure range of 60-105 kg/cm/sup 2/. None of these compounds were effective as platonizer, except lead fluoride, which lowered n value to 0.34 in the lower pressure range. Addition of carbon black along with lead compounds raised burning rates further and reduced n values significantly in the higher pressure regins. A probable mechanism on the role of lead compounds studied has been suggested based on burning rate and DTA results.

  19. Composition and leaching of construction and demolition waste: Inorganic elements and organic compounds

    DEFF Research Database (Denmark)

    Butera, Stefania; Christensen, Thomas Højlund; Astrup, Thomas Fruergaard

    2014-01-01

    Thirty-three samples of construction and demolition waste collected at 11 recycling facilities in Denmark were characterised in terms of total content and leaching of inorganic elements and presence of the persistent organic pollutants PCBs and PAHs. Samples included (i) "clean" (i.e. unmixed......) concrete waste, (ii) mixed masonry and concrete, (iii) asphalt and (iv) freshly cast concrete cores; both old and newly generated construction and demolition waste was included. PCBs and PAHs were detected in all samples, generally in non-critical concentrations. Overall, PAHs were comparable to background...... for leaching, was observed indicating that the number of analysed samples may be critical in relation to decisions regarding management and utilisation of the materials. Higher leaching of chromium, sulphate and chloride were observed for masonry-containing and partly carbonated samples, indicating that source...

  20. COSIMA-Rosetta calibration for in-situ characterization of 67P/Churyumov-Gerasimenko cometary inorganic compounds

    CERN Document Server

    Krüger, Harald; Engrand, Cécile; Briois, Christelle; Siljeström, Sandra; Merouane, Sihane; Baklouti, Donia; Fischer, Henning; Fray, Nicolas; Hornung, Klaus; Lehto, Harry; Orthous-Daunay, François-Régis; Rynö, Jouni; Schulz, Rita; Silen, Johan; Thirkell, Laurent; Trieloff, Mario; Hilchenbach, Martin

    2015-01-01

    COSIMA (COmetary Secondary Ion Mass Analyser) is a time-of-flight secondary ion mass spectrometer (TOF-SIMS) on board the Rosetta space mission. COSIMA has been designed to measure the composition of cometary dust grains. It has a mass resolution m/{\\Delta}m of 1400 at mass 100 u, thus enabling the discrimination of inorganic mass peaks from organic ones in the mass spectra. We have evaluated the identification capabilities of the reference model of COSIMA for inorganic compounds using a suite of terrestrial minerals that are relevant for cometary science. Ground calibration demonstrated that the performances of the flight model were similar to that of the reference model. The list of minerals used in this study was chosen based on the mineralogy of meteorites, interplanetary dust particles and Stardust samples. It contains anhydrous and hydrous ferromagnesian silicates, refractory silicates and oxides (present in meteoritic Ca-Al-rich inclusions), carbonates, and Fe-Ni sulfides. From the analyses of these mi...

  1. Synthesis and Characterization of Poly(St-co-BA) Latex with an Organic-Inorganic Hybrid Compound as Emulsifier

    Institute of Scientific and Technical Information of China (English)

    袁俊杰; 周树学; 廖建和; 武利民

    2003-01-01

    A poly (St-co-BA) latex was successfully synthesized by using an organic-inorganic hybrid compound (OIHC), an aliphatic carboxylate sodium/nano-silica composite, as the emulsifier, and investigated by particle size analyzer, transmission electron microscope (TEM), optical contact angle measurement (OCA) and dynamic mechanical analyzer (DMA). It was found that the protective agent, sodium polyacrylate (PA),could obviously improve the polymerization stability and the functional monomer, glycidyl methacrylate (GMA), could enhance the store stability of the latex. The particle size of poly(St-co-BA) latex decreased and then leveled off as OIHC content increased. TEM shows that the prepared polymers were a~:tually organic-inorganic nanocomposites, and these films have better waterproof property than those prepared by traditional poly(St-co-BA) latex or organic silicone modified poly(St-co-BA) latex. The nanocomposite polymer has much higher glass transition temperature than organic silicone modified poly(St-co-BA) polymer containing the same organic silicone content.

  2. Crystal structure of an organic-inorganic hybrid compound based on morpholinium cations and a β-type Anderson polyanion.

    Science.gov (United States)

    Lukianova, Tamara J; Kinzhybalo, Vasyl; Pietraszko, Adam

    2015-11-01

    A new organic-inorganic hybrid compound, penta-morpholinium hexa-hydrogen hexa-molybdoferrate(III) sulfate 3.5-hydrate, (C4H10NO)5[Fe(III)(OH)6Mo6O18](SO4)·3.5H2O, was obtained from an aqueous solution. The polyoxidomolybdate (POM) anion is of the Anderson β-type with a central Fe(III) ion. Three of five crystallographically independent morpholinium cations are disordered over two sets of sites. An intricate network of inter-molecular N-H⋯O and O-H⋯O inter-actions between cations, POMs, sulfate anions and non-coordinating water mol-ecules creates a three-dimensional network structure.

  3. Critical review of the chemistry and thermodynamics of technetium and some of its inorganic compounds and aqueous species

    Energy Technology Data Exchange (ETDEWEB)

    Rard, J.A.

    1983-09-15

    Chemical and thermodynamic data for Technetium (Tc) and some of its inorganic compounds and aqueous species are reviewed here. Major emphasis is given to systems with potential geochemical applications, especially the geochemistry of radioactive waste disposal. Compounds considered include oxides, hydroxides, hydrates oxides, halides, oxyhalides, double halides, and sulfides. The aqueous species considered include those in both noncomplexing media (pertechnetates, technetates, aquo-ions, and hydrolyzed cations) and complexing media (halides, sulfates, and phosphates). Thermodynamic values are recommended for specific compounds and aqueous ions when reliable experimental data are available. Where thermodynamic data are inadequate or unavailable, the chemistry is still discussed to provide information about what needs to be measured, and which chemistry needs to be clarified. A major application of these thermodynamic data will be for chemical equilibrium modeling and for construction of potential-pH diagrams for aqueous solutions. Unfortunately, the present lack of data precludes such calculations for complexing aqueous media. The situation is much better for noncomplexing aqueous media, but the chemistry and thermodynamics of cationic Tc(V) species and hydrolyzed Tc(III) species are poorly understood. 240 references, 6 tables.

  4. 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.

  5. Determination of inorganic nickel compounds in the particulate matter of emissions and workplace air by selective sequential dissolutions.

    Science.gov (United States)

    Profumo, A; Spini, G; Cucca, L; Pesavento, M

    2003-11-12

    A speciation method of inorganic nickel compounds in airborne particulate, based on selective sequential extractions, is described. It allows the separation and the determination of Ni(0), Ni(II) soluble salts such as sulphate and chloride, Ni insoluble compounds such as nickel oxide and sulphide, to which a different toxicity and therefore a different risk are related. The nickel concentration in each fraction was determined by Flame or Furnace Atomic Absorption Spectroscopy. The proposed procedure has been tested first, on synthetic samples prepared with the different nickel compounds, in the presence of atmospherical particulate matter not containing nickel, in order to take into account the possible matrix influence. The speciation was then repeated on four different samples (fly ash deriving from a solid waste incinerator and three RSMS from NIST: Coal Fly ash SRM 1633b, Urban Particulate 1648, Washington Dust 1649), followed by an evaluation of matrix spiking and recovery analyses. Performing multiple analyses of the spiked samples assessed the repeatability of the procedure.

  6. Critical review of the chemistry and thermodynamics of technetium and some of its inorganic compounds and aqueous species

    Energy Technology Data Exchange (ETDEWEB)

    Rard, J.A.

    1983-09-15

    Chemical and thermodynamic data for Technetium (Tc) and some of its inorganic compounds and aqueous species are reviewed here. Major emphasis is given to systems with potential geochemical applications, especially the geochemistry of radioactive waste disposal. Compounds considered include oxides, hydroxides, hydrates oxides, halides, oxyhalides, double halides, and sulfides. The aqueous species considered include those in both noncomplexing media (pertechnetates, technetates, aquo-ions, and hydrolyzed cations) and complexing media (halides, sulfates, and phosphates). Thermodynamic values are recommended for specific compounds and aqueous ions when reliable experimental data are available. Where thermodynamic data are inadequate or unavailable, the chemistry is still discussed to provide information about what needs to be measured, and which chemistry needs to be clarified. A major application of these thermodynamic data will be for chemical equilibrium modeling and for construction of potential-pH diagrams for aqueous solutions. Unfortunately, the present lack of data precludes such calculations for complexing aqueous media. The situation is much better for noncomplexing aqueous media, but the chemistry and thermodynamics of cationic Tc(V) species and hydrolyzed Tc(III) species are poorly understood. 240 references, 6 tables.

  7. High-throughput screening of inorganic compounds for the discovery of novel dielectric and optical materials

    Science.gov (United States)

    Petousis, Ioannis; Mrdjenovich, David; Ballouz, Eric; Liu, Miao; Winston, Donald; Chen, Wei; Graf, Tanja; Schladt, Thomas D.; Persson, Kristin A.; Prinz, Fritz B.

    2017-01-01

    Dielectrics are an important class of materials that are ubiquitous in modern electronic applications. Even though their properties are important for the performance of devices, the number of compounds with known dielectric constant is on the order of a few hundred. Here, we use Density Functional Perturbation Theory as a way to screen for the dielectric constant and refractive index of materials in a fast and computationally efficient way. Our results constitute the largest dielectric tensors database to date, containing 1,056 compounds. Details regarding the computational methodology and technical validation are presented along with the format of our publicly available data. In addition, we integrate our dataset with the Materials Project allowing users easy access to material properties. Finally, we explain how our dataset and calculation methodology can be used in the search for novel dielectric compounds. PMID:28140408

  8. Sulfur Isotope Exchange between S-35 Labeled Inorganic Sulfur-Compounds in Anoxic Marine-Sediments

    DEFF Research Database (Denmark)

    FOSSING, H.; THODEANDERSEN, S.; JØRGENSEN, BB

    1992-01-01

    Isotope exchange reactions between S-35-labeled sulfur compounds were studied in anoxic estuarine sediment slurries at 21-degrees-C and pH 7.4-7.7. Two experiments labeled with radioactive elemental sulfur (S-35-degrees) and one labeled with radioactive sulfate ((SO42-)-S-35) were performed as time...

  9. Comparative evaluation of short-term toxicity of inorganic arsenic compounds on Artemia salina.

    Science.gov (United States)

    GuŢu, Claudia Maria; Olaru, Octavian Tudorel; Purdel, Nicoleta Carmen; Ilie, Mihaela; NeamŢu, Marius Cristian; Dănciulescu Miulescu, Rucsandra; Avramescu, Elena Taina; Margină, Denisa Marilena

    2015-01-01

    The study aimed to assess the short-term effects exerted by two inorganic arsenic species (arsenite and arsenate) on Artemia salina after 24, 48 and 72 h. The dose-lethality curves obtained indicate that the lethality induced by arsenite was higher than by arsenate. The lowest observed effect concentration for arsenite (0.5 μg/mL) is similar with the no observed effect concentration for arsenate, thus indicating that the toxicity of arsenite is higher compared with arsenate. Also, the lethal concentration 50 values confirm that arsenite induced about 1.24-fold higher toxicity than arsenate at 24 h and about three-fold higher toxicity at 48 h and 72 h of exposure. Both LC50 (lethal concentration 50) values are indicating negligible effects exhibited by arsenic at this trophic level after short-term exposure. The predicted no effect concentration in the surface aquatic compartment corresponds to 10.38 μg/L, similar to the limit imposed by Directive 98/83/EC.

  10. Composition and leaching of construction and demolition waste: inorganic elements and organic compounds.

    Science.gov (United States)

    Butera, Stefania; Christensen, Thomas H; Astrup, Thomas F

    2014-07-15

    Thirty-three samples of construction and demolition waste collected at 11 recycling facilities in Denmark were characterised in terms of total content and leaching of inorganic elements and presence of the persistent organic pollutants PCBs and PAHs. Samples included (i) "clean" (i.e. unmixed) concrete waste, (ii) mixed masonry and concrete, (iii) asphalt and (iv) freshly cast concrete cores; both old and newly generated construction and demolition waste was included. PCBs and PAHs were detected in all samples, generally in non-critical concentrations. Overall, PAHs were comparable to background levels in urban environments. "Old" and "new" concrete samples indicated different PCB congener profiles and the presence of PCB even in new concrete suggested that background levels in raw materials may be an issue. Significant variability in total content of trace elements, even more pronounced for leaching, was observed indicating that the number of analysed samples may be critical in relation to decisions regarding management and utilisation of the materials. Higher leaching of chromium, sulphate and chloride were observed for masonry-containing and partly carbonated samples, indicating that source segregation and management practices may be important. Generally, leaching was in compliance with available leaching limits, except for selenium, and in some cases chromium, sulphate and antimony. Copyright © 2014 Elsevier B.V. All rights reserved.

  11. [Effects of Organic and Inorganic Slow-Release Compound Fertilizer on Different Soils Microbial Community Structure].

    Science.gov (United States)

    Wang, Fei; Yuan, Ting; Gu, Shou-kuan; Wang, Zheng-yin

    2015-04-01

    As a new style fertilizer, slow-control release fertilizer had been an important subject in recent years, but few researches were about soil microbial community structure diversity. Phospholipid fatty acid method was used to determined the microbial community structure diversity of acid soil and slight alkaline soil applied with slow-release compound fertilizer (SRF), chemical fertilizer (CF) and common compound fertilizer (CCF) at the 10th, 30th, 60th and 90th day under the constant temperature incubation condition. Results indicated that various bacteria (i. e 13:0, i14:0,14:0, i15:0, a15:0, i16:0, 16:12OH, 16:1w5c,16:0, i17:0, a17:0, cy17:0, 17:02OH, i18:0, 18:0 and cy19:0w8c), two actinomycetes (10Me17:0 and 10Me18:0) and only one fungus (18:1 w9c) were detected in two soils after applying slow-release compound fertilizer and other fertilizers during the whole incubation period. SRF could significantly increase the fungi PLFA content by 8.3% and 6.8% at the early stage (the 10th day and 30th day) compared with CF, as well as significantly increase by 22.7% and 17.1% at the late stage (the 60th day and 90th day) compared with CCF in acid soil. SRF significantly increased bacteria, fungi and gram positive bacteria compared with CF and CCF in incubation period (except at the 30th day) in slight alkaline soil. SRF could significantly improve the ratio of normal saturated fatty acid and monounsaturated fatty acid at the 30th day and 90th days in acid soil compared with no fertilizer (CK), CF and CCF, while as to slight alkaline soil, SRF was significantly greater than that of CK, CF and CCF only at the 60th day. SRF could significantly decrease the ratio of iso PLFA and anteiso PLFA in acid soil (in 30-90 days) and slight alkaline soil (in 10-60 days). For two soils PLFA varieties, contents and ratios of microbial community, slow-release compound fertilizer increased soil microbial PLFA varieties and contents, and decreased the influence to microbial survival

  12. Inorganic-organic hybrid compounds based on octamolybdates and multidentate N-donor ligand: syntheses, structures, photoluminescence and photocatalysis.

    Science.gov (United States)

    Kan, Wei-Qiu; Yang, Jin; Liu, Ying-Ying; Ma, Jian-Fang

    2012-08-28

    Six inorganic-organic hybrid compounds, namely, [Cu(2)(2,4'-tmbpt)(2)(β-Mo(8)O(26))(H(2)O)(2)]·7H(2)O (1), [Cu(2,4'-tmbpt)(γ-Mo(8)O(26))(0.5)(H(2)O)]·H(2)O (2), [Co(2,4'-Htmbpt)(2)(γ-Mo(8)O(26))(H(2)O)(2)] (3), [Zn(2,4'-Htmbpt)(2)(γ-Mo(8)O(26))(H(2)O)(2)] (4), [Ni(2,4'-tmbpt)(α-Mo(8)O(26))(0.5)(H(2)O)]·2.5H(2)O (5) and [Ag(2,4'-Htmbpt)(β-Mo(8)O(26))(0.5)] (6), have been synthesized under hydrothermal conditions (2,4'-tmbpt = 1-((1H-1,2,4-triazol-1-yl)methyl)-3-(2-pyridyl)-5-(4-pyridyl)-1,2,4-triazole). The structures of compounds 1-6 have been determined by single-crystal X-ray diffraction analyses and characterized by infrared spectra (IR), elemental analyses, powder X-ray diffraction (PXRD) analyses and thermogravimetric analyses (TGA). Compound 1 shows a 3D (3,4)-connected framework constructed by the 2D Cu(II)-organic fragments and [β-Mo(8)O(26)](4-) anions. Compound 2 exhibits a 2D layer structure based on Cu(II)-organic chains and [γ-Mo(8)O(26)] chains. The layers are extended into a 3D supramolecular framework by hydrogen-bonding interactions. Compounds 3 and 4 are isostructural, and display 1D chain structures. The chains are further interlinked by hydrogen-bonding interactions to form 3D supramolecular architectures. Compound 5 shows a 3D framework based on the 2D Ni(II)-organic fragments and [α-Mo(8)O(26)](4-) anions. In compound 6, the 1D chains constructed by the Ag(I) ions, 2,4'-Htmbpt ligands and [β-Mo(8)O(26)](4-) anions are extended by hydrogen-bonding interactions into a 2D supramolecular layer. Each layer threads into the adjacent layers, yielding a 2D → 3D interdigitated structure. Moreover, the photoluminescent properties of 4 and 6, the optical band gaps of 1-6, and the photocatalytic properties of 1-6 have also been investigated.

  13. Anomalous luminescence of Eu sup 2 sup + and Yb sup 2 sup + in inorganic compounds

    CERN Document Server

    Dorenbos, P

    2003-01-01

    In many compounds the broadband emission of Eu sup 2 sup + and Yb sup 2 sup + is subject to a very large (0.6-1.2 eV) Stokes shift and it behaves peculiarly with temperature change. Conduction band states of the host compound are involved in this 'anomalous' emission. Cases of anomalous emission are identified and the conditions for it to occur studied. Clear trends with the size of the lanthanide ion, the size of the site occupied, the size of anions in the compound, and the binding strength of oxygen ligands were found. The trends are interpreted by models involving the Madelung potential and Pauling repulsion at the lanthanide site together with the Coulomb and isotropic exchange interactions within the lanthanide ion. The results provide information on the approximate location of the lowest 4f sup n sup - sup 1 5d level relative to the bottom of the conduction band. The systematic variation with type of lanthanide and host lattice is discussed. Combining the results with information on the systematic vari...

  14. Influence of inorganic and organic iron compounds on parameters of cell growth and survival in human colon cells.

    Science.gov (United States)

    Klenow, Stefanie; Pool-Zobel, Beatrice L; Glei, Michael

    2009-04-01

    Increased risk for development of colon cancer is associated with red meat intake and iron toxicity is discussed for one underlying mechanism. Anyhow, for iron itself only limited evidence is found. In this study, effects of different iron compounds on proliferation of HT29 carcinoma and LT97 adenoma human colon cells were investigated. After treatment of cells with inorganic (ferrous sulfate: FeSO4 and ferric nitrilotriacetate: FeNTA) and organic (hemoglobin and hemin) iron sources (24-72 h), number of cells and metabolic activity were measured. Under normal cell culture conditions, neither iron compound elevated cell growth in either cell line with the exception of FeNTA which induced LT97 cell growth significantly. Distinct inhibition of cell proliferation was measured for organic iron. Serum-free incubation of HT29 cells revealed growth promoting properties of iron under deficiency. Even though organic iron, especially hemin, was a potent growth factor, both substances showed also dose-dependent cytotoxic effects. In conclusion, these data emphasize that not iron itself, but merely organic iron may promote carcinogenic events. Since promotion of proliferation was only detectable under deficiency, cytotoxic properties of organic iron may be of more importance in colon carcinogenesis.

  15. Induction by mercury compounds of metallothioneins in mouse tissues: inorganic mercury accumulation is not a dominant factor for metallothionein induction in the liver.

    Science.gov (United States)

    Yasutake, Akira; Nakamura, Masaaki

    2011-06-01

    Among the naturally occurring three mercury species, metallic mercury (Hg(0)), inorganic mercury (Hg(II)) and methylmercury (MeHg), Hg(II) is well documented to induce metallothionein (MT) in tissues of injected animals. Although Hg(0) and MeHg are considered to be inert in terms of directly inducing MT, MT can be induced by them after in vivo conversion to Hg(II) in an animal body. In the present study we examined accumulations of inorganic mercury and MT inductions in mouse tissues (brain, liver and kidney) up to 72 hr after treatment by one of three mercury compounds of sub-lethal doses. Exposure to mercury compounds caused significant mercury accumulations in mouse tissues examined, except for the Hg(II)-treated mouse brain. Although MeHg caused the highest total mercury accumulation in all tissues among mercury compounds, the rates of inorganic mercury were less than 10% through the experimental period. MT inductions that depended on the inorganic mercury accumulation were observed in kidney and brain. However, MT induction in the liver could not be accounted for by the inorganic mercury accumulation, but by plasma IL6 levels, marked elevation of which was observed in Hg(II) or MeHg-treated mouse. The present study demonstrated that MT was induced in mouse tissues after each of three mercury compounds, Hg(0), Hg(II) and MeHg, but the induction processes were different among tissues. The induction would occur directly through accumulation of inorganic mercury in brain and kidney, whereas the hepatic MT might be induced secondarily through mercury-induced elevation in the plasma cytokines, rather than through mercury accumulation in the tissue.

  16. The electronic structure of organic-inorganic hybrid compounds : (NH4)(2)CuCl4, (CH3NH3)(2)CuCl4 and (C2H5NH3)(2)CuCl4

    NARCIS (Netherlands)

    Zolfaghari, P.; de Wijs, G. A.; de Groot, R. A.

    2013-01-01

    Hybrid organic-inorganic compounds are an intriguing class of materials that have been experimentally studied over the past few years because of a potential broad range of applications. The electronic and magnetic properties of three organic-inorganic hybrid compounds with compositions (NH4)(2)CuCl4

  17. The electronic structure of organic-inorganic hybrid compounds : (NH4)(2)CuCl4, (CH3NH3)(2)CuCl4 and (C2H5NH3)(2)CuCl4

    NARCIS (Netherlands)

    Zolfaghari, P.; de Wijs, G. A.; de Groot, R. A.

    2013-01-01

    Hybrid organic-inorganic compounds are an intriguing class of materials that have been experimentally studied over the past few years because of a potential broad range of applications. The electronic and magnetic properties of three organic-inorganic hybrid compounds with compositions

  18. Comparative study on the pharmacokinetics of inorganic and organic iron compounds in broiler chickens

    Directory of Open Access Journals (Sweden)

    Dimitrichka Dimitrova

    2014-03-01

    Full Text Available The pharmacokinetics of ferrous methionate and ferrous sulphate was investigated in broiler chickens after intravenous injection and crop intubation. The iron compounds were injected intravenously in v. brachialis. After 20-day “wash-out” period the ferrous methionate and ferrous sulphate were administered again by an elastic silicone tube into the crop. The serum concentrations of the iron were determined with bioanalyser. Two pharmacokinetic approaches were used – compartmental and non-compartmental analysis. After i.v. injection we found statistically significantly longer and better distribution of the iron contained in the ferrous methionate compared to the ferrous sulphate. The АUC0→∞ was statistically significantly higher in the ferrous methionate. In the alimentary tract of broiler chickens, ferrous methionate was absorbed more rapidly than ferrous sulfate. It was also distributed at a higher volume as compared to the ferrous sulfate.

  19. The occurrence and representation of three-centre two-electron bonds in covalent inorganic compounds.

    Science.gov (United States)

    Green, Jennifer C; Green, Malcolm L H; Parkin, Gerard

    2012-12-07

    Although compounds that feature 3-centre 2-electron (3c-2e) bonds are well known, there has been no previous effort to classify the interactions according to the number of electrons that each atom contributes to the bond, in a manner analogous to the classification of 2-centre 2-electron (2c-2e) bonds as either normal covalent or dative covalent. This article provides an extension to the Covalent Bond Classification (CBC) method by categorizing 3c-2e interactions according to whether (i) the two electrons are provided by one or by two atoms and (ii) the central bridging atom provides two, one, or zero electrons. Class I 3c-2e bonds are defined as those in which two atoms each contribute one electron to the 3-centre orbital, while Class II 3c-2e bonds are defined as systems in which the pair of electrons are provided by a single atom. Class I and Class II 3c-2e interactions can be denoted by structure-bonding representations that employ the "half-arrow" notation, which also provides a convenient means to determine the electron count at a metal centre. In contrast to other methods of electron counting, this approach provides a means to predict metal-metal bond orders that are in accord with theory. For example, compounds that feature symmetrically bridging carbonyl ligands do not necessarily have to be described as "ketone derivatives" because carbon monoxide can also serve as an electron pair donor to two metal centres. This bonding description also provides a simple means to rationalize the theoretical predictions of the absence of M-M bonds in molecules such as Fe(2)(CO)(9) and [CpFe(CO)(2)](2), which are widely misrepresented in textbooks as possessing M-M bonds.

  20. Complex Organic and Inorganic Compounds in Shells of Lithium-rich K Giant Stars

    CERN Document Server

    de la Reza, Ramiro; Oliveira, Isa; Rengaswamy, Sridharan

    2015-01-01

    Hydrocarbon organic material, as found in the interstellar medium, exists in complex mixtures of aromatic and aliphatic forms. It is considered to be originated from carbon enriched giant stars during their final stages of evolution, when very strong mass loss occurs in a few thousand years on their way to become planetary nebulae. We show here that the same organic compounds appear to be formed in previous stages of the evolution of giant stars. More specifically, during the first ascending giant branch K-type stars. According to our model this happens only when these stars are being abruptly enriched with lithium together with the formation of a circumstellar shell with a strong mass loss during just a few thousand years. This sudden mass loss is, on an average, a thousand times larger than that of normal Li-poor K giant stars. This shell would later be detached, specially when the star stops its Li enrichment and a rapid photospheric Li depletion occurs. In order to gain extra carbon-based material to form...

  1. A two-dimensional organic–inorganic hybrid compound, poly[(ethylenediaminetri-μ-oxido-oxidocopper(IImolybdenum(VI

    Directory of Open Access Journals (Sweden)

    Mehtap Emirdag-Eanes

    2008-10-01

    Full Text Available A new organic–inorganic two-dimensional hybrid compound, [CuMoO4(C2H8N2], has been hydrothermally synthesized at 443 K. The unit cell contains layers composed of CuN2O4 octahedra and MoO4 tetrahedra. Corner-sharing MoO4 and CuN2O4 polyhedra form CuMoO4 bimetallic sites that are joined together through O atoms, forming an edge-sharing Cu2Mo2O4 chain along the c axis. The one-dimensional chains are further linked through bridging O atoms that join the Cu and Mo atoms into respective chains along the b axis, thus establishing layers in the bc plane. The ethylenediamine ligand is coordinated to the Cu atom through its two N atoms and is oriented perpendicularly to the two-dimensional –Cu—O—Mo– layers. The average distance between adjacent layers, as calculated by consideration of the closest and furthest distances between two layers, is 8.7 Å. The oxidation states of the Mo and Cu atoms of VI and II, respectively, were confirmed by bond-valence sum calculations.

  2. Experimental and theoretical study of AC electrical conduction mechanisms of Organic-inorganic hybrid compound Bis (4-acetylanilinium) tetrachlorocadmiate (II)

    Science.gov (United States)

    Jellibi, A.; Chaabane, I.; Guidara, K.

    2016-06-01

    A new organic-inorganic bis (4-acetylaniline) tetrachlorocadmate [C8H10NO]2[CdCl4] can be obtained by slow evaporation at room temperature and characterized by X-ray powder diffraction. It crystallized in an orthorhombic system (Cmca space group). The material electrical properties were characterized by impedance spectroscopy technique in the frequency range from 209 Hz-5 MHz and temperature 413 to 460 K. Besides, the impedance plots show semicircle arcs at different temperatures and an electrical equivalent circuit has been proposed to interpret the impedance results. The circuits consist of the parallel combination of a resistance (R), capacitance (C) and fractal capacitance (CPE). The variation of the exponent s as a function of temperature suggested that the conduction mechanism in Bis (4-acetylanilinium) tetrachlorocadmiate compound is governed by two processes which can be ascribed to a hopping transport mechanism: correlated barrier hopping (CBH) model below 443 K and the small polaron tunneling (SPT) model above 443 K.

  3. Thermal properties study on the ablation materials of inorganic silicon compound from organosilicone in high percent conversion

    Institute of Scientific and Technical Information of China (English)

    CUI MengZhong; WANG WenHua

    2007-01-01

    The new type of silicone rubber prepared by organosilicon polymer containing special groups presents the tensile strength of 3.92 MPa and the elongation at break of 285%. Compared with Sylgard(r)184 silicone rubber (Dow Corning Corporation), it has better high temperature resistance and almost no weightlessness from room temperature to 430℃. Thermogravimetric analysis was conducted to research the thermal degradation at different temperatures and the heat pyrolysis products were trace determined by FT-IR. The results show that with the increase of temperature, the organic groups of products are gradually decomposed. Organosilicon rubber is gradually changed into the typical inorganic SiCO compounds in the process of pyrolysis. Elemental analysis and X-ray photoelectron spectroscopy results show that the pyrolyzates are mainly composed of Si, C and O elements above 1050℃. X-ray diffraction analysis showes that partial β-SiC crystal structure is brought about gradually from the pyrolysis products at 1050℃ to 1500℃ under nitrogen atmosphere. With the treatment temperature rising, the crystallinity of SiC and cristobalite obviously increases.

  4. Differential effects of organic and inorganic selenium compounds on adenosine deaminase activity and scavenger capacity in cerebral cortex slices of young rats.

    Science.gov (United States)

    Bitencourt, P E R; Bellé, L P; Bonfanti, G; Cargnelutti, L O; de Bona, K S; Silva, P S; Abdalla, F H; Zanette, R A; Guerra, R B; Funchal, C; Moretto, M B

    2013-09-01

    Selenium (Se) has anti-inflammatory and antioxidant properties and is necessary for the development and normal function of the central nervous system. This study was aimed to compare the in vitro effects of 3-methyl-1-phenyl-2-(phenylseleno)oct-2-en-1-one (C21H2HOSe; organoselenium) and sodium selenate (inorganic Se) on adenosine deaminase (ADA) activity, cell viability, lipid peroxidation, scavenger of nitric oxide (NO) and nonprotein thiols (NP-SH) content in the cerebral cortex slices of the young rats. A decrease in ADA activity was observed when the slices were exposed to organoselenium at the concentrations of 1, 10 and 30 µM. The same compound showed higher scavenger capacity of NO than the inorganic compound. Inorganic Se was able to protect against sodium nitroprusside-induced oxidative damage and increased the NP-SH content. Both the compounds displayed distinctive antioxidant capacities and were not cytotoxic for the cerebral cortex slices in the conditions tested. These findings are likely to be related to immunomodulatory and antioxidant properties of this compound.

  5. 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.

  6. (CH3 NH3 )2 PdCl4 : A Compound with Two-Dimensional Organic-Inorganic Layered Perovskite Structure.

    Science.gov (United States)

    Huang, Tang Jiao; Thiang, Zhang Xian; Yin, Xuesong; Tang, Chunhua; Qi, Guojun; Gong, Hao

    2016-02-01

    The synthesis of previously unknown perovskite (CH3 NH3 )2 PdCl4 is reported. Despite using an organic cation with the smallest possible alkyl group, a 2D organic-inorganic layered Pd-based perovskites was still formed. This demonstrates that Pd-based 2D perovskites can be obtained even if the size of the organic cation is below the size limit predicted by the Goldschmidt tolerance-factor formula. The (CH3 NH3 )2 PdCl4 phase has a bulk resistivity of 1.4 Ω cm, a direct optical gap of 2.22 eV, and an absorption coefficient on the order of 10(4)  cm(-1) . XRD measurements suggest that the compound is moderately stable in air, an important advantage over several existing organic-inorganic perovskites that are prone to phase degradation problems when exposed to the atmosphere. Given the recent interest in organic-inorganic perovskites, the synthesis of this new Pd-based organic-inorganic perovskite may be helpful in the preparation and understanding of other organic-inorganic perovskites. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. Sustainable Non-Metallic Building Materials

    Directory of Open Access Journals (Sweden)

    Svetlana Tretsiakova-McNally

    2010-01-01

    Full Text Available Buildings are the largest energy consumers and greenhouse gases emitters, both in the developed and developing countries. In continental Europe, the energy use in buildings alone is responsible for up to 50% of carbon dioxide emission. Urgent changes are, therefore, required relating to energy saving, emissions control, production and application of materials, use of renewable resources, and to recycling and reuse of building materials. In addition, the development of new eco-friendly building materials and practices is of prime importance owing to the growing environmental concerns. This review reflects the key tendencies in the sector of sustainable building materials of a non-metallic nature that have occurred over the past decade or so.

  8. Inorganic-organic hybrid compounds based on face-sharing octahedral [PbI3]∞ chains: self-assemblies, crystal structures, and ferroelectric, photoluminescence properties.

    Science.gov (United States)

    Duan, Hai-Bao; Zhao, Hai-Rong; Ren, Xiao-Ming; Zhou, Hong; Tian, Zheng-Fang; Jin, Wan-Qin

    2011-02-28

    Eight inorganic-organic hybrid compounds with a formula of [R-Bz-1-APy][PbI(3)] (R-Bz-1-APy(+) = mono-substituted benzylidene-1-aminopyridinium Schiff base derivative; R = m-CN (1), m-CH(3) (2), H (3), p-F (4), p-Cl (5), p-Br (6), o-Cl (7), o-Br (8)) have been synthesized and characterized structurally. The common characteristic of the crystal structures of 1-8 is that the inorganic components form straight and face-sharing octahedral [PbI(3)](∞) chains and the Schiff base cations surround the [PbI(3)](∞) chains to form molecular stacks. The substituent (R) on the phenyl ring of the Schiff base cation clearly influences the packing structures of 1-8, and the hybrid compound crystallizes in the space group P6(3) when R = CN (1) in the meta-position of the phenyl ring, and in a central symmetric space group when R is in the ortho- or para-position of the phenyl ring. The conformation of the Schiff base cation is related to the R position, and the dihedral angle between the phenyl and pyridyl rings increases in the order of para- inorganic [PbI(3)](∞) chain in the para-substituted hybrid compounds, and perpendicular to the straight inorganic [PbI(3)](∞) chain in the ortho-substituted hybrid compounds. 1 is second harmonic generation (SHG) active with a comparable response as that of urea and also exhibits ferroelectricity with larger P(s) and P(r) values; 1-8 emit multi-band luminescence in the 300-650 nm regions under the excitation of ultraviolet light.

  9. Submicron magnetite grains and carbon compounds in Martian meteorite ALH84001: inorganic, abiotic formation by shock and thermal metamorphism.

    Science.gov (United States)

    Treiman, Allan H

    2003-01-01

    Purported biogenic features of the ALH84001 Martian meteorite (the carbonate globules, their submicron magnetite grains, and organic matter) have reasonable inorganic origins, and a comprehensive hypothesis is offered here. The carbonate globules were deposited from hydrothermal water, without biological mediation. Thereafter, ALH84001 was affected by an impact shock event, which raised its temperature nearly instantaneously to 500-700K, and induced iron-rich carbonate in the globules to decompose to magnetite and other minerals. The rapidity of the temperature increase caused magnetite grains to nucleate in abundance; hence individual crystals were very small. Nucleation and growth of magnetite crystals were fastest along edges and faces of the precursor carbonate grains, forcing the magnetite grains to be platy or elongated, including the "truncated hexa-octahedra" shape. ALH84001 had formed at some depth within Mars where the lithostatic pressure was significantly above that of Mars' surface. Also, because the rock was at depth, the impact heat dissipated slowly. During this interval, magnetite crystals approached chemical equilibria with surrounding minerals and gas. Their composition, nearly pure Fe(3)O(4), reflects those of equilibria; elements that substitute into magnetite are either absent from iron-rich carbonate (e.g., Ti, Al, Cr), or partitioned into other minerals during magnetite formation (Mg, Mn). Many microstructural imperfections in the magnetite grains would have annealed out as the rock cooled. In this post-shock thermal regime, carbon-bearing gas from the decomposition of iron carbonates reacted with water in the rock (or from its surroundings) to produce organic matter via Fischer-Tropschlike reactions. Formation of such organic compounds like polycyclic aromatic hydrocarbons would have been catalyzed by the magnetite (formation of graphite, the thermochemically stable phase, would be kinetically hindered).

  10. Non-metallic, non-Fermi-liquid resistivity of FeCrAs from 0 to 17 GPa.

    Science.gov (United States)

    Tafti, F F; Wu, W; Julian, S R

    2013-09-25

    An unusual, non-metallic resistivity of the 111 iron-pnictide compound FeCrAs is shown to be relatively unchanged under pressures of up to 17 GPa. Combined with our previous finding that this non-metallic behaviour persists from at least 80 mK to 800 K, this shows that the non-metallic phase is exceptionally robust. Antiferromagnetic order, with a Néel temperature TN ∼ 125 K at ambient pressure, is suppressed by pressure at a rate of 7.0 ± 0.4 K GPa(-1), falling to ∼50 K at 10 GPa. We conclude that the formation of a spin-density-wave gap at TN does not play an important role in the non-metallic resistivity of FeCrAs at low temperatures.

  11. Crystal structure, vibrational studies and optical properties of a new organic-inorganic hybrid compound (C₁₀H₂₈N₄)CuCl₅Cl⋅4H₂O.

    Science.gov (United States)

    Kessentini, A; Belhouchet, M; Suñol, J J; Abid, Y; Mhiri, T

    2015-01-01

    A new organic-inorganic hybrid material, 1,4-bis(3-ammoniumpropyl) piperazinium pentachloridocuprate(II) chloride tetrahydrate [(C₁₀H₂₈N₄)CuCl₅Cl⋅4H₂O], has been synthesized and characterized by X-ray diffraction, UV-visible absorption, Infrared and Raman spectroscopy. The compound crystallizes in the orthorhombic system and Pnma space group with a=8.18 (3)Å, b=10.96 (5)Å, c=21.26 (9)Å, V=2254.3 (15)Å(3). In this structure, the Cu(2+) ion, surrounded by five chlorides, adopts the square pyramidal coordination geometry. The structure of this compound consists of tetraprotonated 1,4-bis(3-ammoniumpropyl) piperazinium cations and the anionic sublattice is built up of isolated, square pyramid [CuCl₅](3)(-) units, chloride ion Cl(-) and water molecules connected with each other by hydrogen bonds. Organic and inorganic entities are interconnected by means of hydrogen bonding contacts [NH⋯O(Cl), O(W)H⋯Cl and O(W)H⋯O]. Furthermore, the room temperature IR and Raman spectra of the title compound were recorded and analyzed on the basis of literature data. The optical study was also investigated by UV-Vis absorption. In fact, the organic-inorganic hybrid crystal thin film can be easily prepared by spin-coating method from the ethanol solution of the (C₁₀H₂₈N₄)CuCl₅Cl⋅4H₂O hybrid compound and it showed absorptions characteristics of CuCl based layered compounds centered at 275 and 374 nm.

  12. pH-dependent assembly of two inorganic-organic hybrid compounds based on octamolybdates: an unusual intercalated layer and a 3D 4-connected framework.

    Science.gov (United States)

    Liu, Hai-Yan; Yang, Jin; Liu, Ying-Ying; Ma, Jian-Fang

    2012-09-07

    Two novel inorganic-organic hybrid compounds based on octamolybdates, namely, [Cu(H(2)L)(2)(γ-Mo(8)O(26))]·(Mo(6)O(19))·2H(2)O (1) and [Cu(H(2)L)(γ-Mo(8)O(26))(H(2)O)(2)]·5H(2)O (2), where L = 1,1'-(1,5-pentanediyl)bis[2-(4-pyridyl)benzimidazole], have been successfully synthesized at different pH values under hydrothermal conditions. Compound 1, which is hydrothermally prepared at pH ≈ 3.5, exhibits an entirely new type of intercalated layer. The nanosized hexamolybdate anions as guests are introduced into the layers. When the pH value is adjusted to 2, a structurally-different complex 2 was obtained. Compound 2 shows a unique 3D 4-connected framework constructed by inorganic layers and H(2)L(2+) ligands as bridges. The two compounds were characterized by elemental analyses, IR spectra and TGA. In addition, the electrochemical properties of 1-modified carbon paste electrode (CPE) have also been investigated in 1 M H(2)SO(4) aqueous solution.

  13. Controllable Assembly of Vanadium-Containing Polyoxoniobate-Based Three-Dimensional Organic-Inorganic Hybrid Compounds and Their Photocatalytic Properties.

    Science.gov (United States)

    Hu, Jufang; Wang, Yin; Zhang, Xinning; Chi, Yingnan; Yang, Song; Li, Jikun; Hu, Changwen

    2016-08-01

    The controllable synthesis of two vanadium-containing polyoxoniobate-based three-dimensional organic-inorganic hybrid compounds, [Co(pn)2]4[HPNb10V(IV)2O40(V(IV)O)4]·17H2O (1) and [Co(pn)2]5[PNb12O40(V(IV)O)6](OH)7·15H2O (2), where pn = 1,2-diaminopropane, is realized by changing the hydrothermal temperature or adding N-(aminoethyl)piperazine as an additive. Both compounds 1 and 2 are structurally characterized by single-crystal/powder X-ray diffraction and IR and X-ray photoelectron spectroscopy. Compound 1 features a new divanadium-substituted Keggin polyoxoniobate capped by four vanadyl groups, and the polyanion in 2 exhibits the highest coordination number (10-connected) in polyoxoniobate chemistry. Moreover, the photocatalytic activities of 1 and 2 for hydrogen evolution are preliminarily assessed.

  14. Hydrothermal Synthesis and Structural Characterization of a Novel Organic-Inorganic Hybrid Compound {[Cu(2,2'-bpy)2]2-Mo8O26}

    Institute of Scientific and Technical Information of China (English)

    WANG,Yong-Hui(王永慧); CHEN,Li-Dong(陈立东); HU,Chang-Wen(胡长文); WANG,En-Bo(王恩波); JIA,Heng-Qing(贾恒庆); HU,Ning-Hai(胡宁海)

    2002-01-01

    A novel organic-inorganic hybrid compound { [ Cu (2, 2'-bpy)2 ]2Mo8O26} has been hydrothermally synthesized and structurally characterized by single-crystal X-ray diffraction.The compound crystallizes in the orthorhombic space group,Pna21, with a= 2.4164(5), b = 1.8281(4), c = 1.1877(2)nm, V=5.247(2)nm3, Z=4, andfinal R1=0.0331, wR2 =0.0727. The structure consists of discrete {[Cu(2,2'-bpy)2]2Mo8O26} clusters, constructed from a β-octamolybdate subunit [ Mo8O26]4- covalently bonded to two [ Cu ( 2, 2'-bpy )2]2+ coordination complex rations via bridging oxo groups. In addition, the spectroscopic properties and thermal behavior of this compound have been investigated by spectroscopic techniques (UV-vis, IR, Raman and EPR spectra) and TG analysis.

  15. The electronic structure of organic-inorganic hybrid compounds: (NH₄)₂CuCl₄, (CH₃NH₃)₂CuCl₄ and (C₂H₅NH₃)₂CuCl₄.

    Science.gov (United States)

    Zolfaghari, P; de Wijs, G A; de Groot, R A

    2013-07-24

    Hybrid organic-inorganic compounds are an intriguing class of materials that have been experimentally studied over the past few years because of a potential broad range of applications. The electronic and magnetic properties of three organic-inorganic hybrid compounds with compositions (NH4)2CuCl4, (CH3NH3)2CuCl4 and (C2H5NH3)2CuCl4 are investigated for the first time with density functional theory plus on-site Coulomb interaction. A strong Coulomb interaction on the copper causes a relatively weak exchange coupling within the layers of the octahedral network, in good agreement with experiment. The character of the exchange interaction (responsible for magnetic behavior) is analyzed. The calculations reveal that (C2H5NH3)2CuCl4 has the strongest Jahn-Teller (JT) distortion in comparison with the two other compounds. The easy axis of magnetization is investigated, showing a weak anisotropic interaction between inter-layer Cu(2+) ions in the (C2H5NH3)2CuCl4 structure. Orbital ordering is concluded from our partial density of states calculations: a cooperation of the JT distortion with an antiferro-distortive pattern.

  16. Concentrations of selected trace inorganic constituents and synthetic organic compounds in the water-table aquifers in the Memphis area, Tennessee

    Science.gov (United States)

    McMaster, B.W.; Parks, William Scott

    1988-01-01

    Water quality samples for analysis of selected trace inorganic constituents and synthetic organic compounds were collected from 29 private or observation wells in alluvium and fluvial deposits of Quaternary and Tertiary Age. The alluvium and fluvial deposits are the water table aquifers in the Memphis area. In addition, nine wells were installed in Memphis Light, Gas and Water Division well fields so that samples could be collected and analyzed to characterize the quality of water in the fluvial deposits at these well fields. Samples from seven of these wells (two were dry) were analyzed for major constituents and properties of water as well as for selected trace inorganic constituents and synthetic organic compounds. Analyses of the water from most of the 36 wells sampled indicated ranges in concentration values for the trace inorganic constituents that agreed with those previously known, although some new maximum values were established. The analysis of water from four wells indicated that the water is or may be contaminated. Concentrations of barium (1,400 micrograms/L -- ug/L), strontium (1,100 ug/L), and arsenic (15 ug/L), along with specific conductance (1,420 microsiemens/centimeter--us/cm) were in water from one well in the alluvium. Low concentrations (0.02 to 0.04 ug/L) of the pesticides aldrin, DDT, endosulfan, and perthane were present in water from two wells in the fluvial deposits. Water from one of these wells also contained 1,1,1 trichloroethane (4.4 ug/L). Analysis of water from another well in the fluvial deposits indicated values for specific conductance (1,100 uS/cm), alkalinity (508 milligrams per liter -- mg/L -- as CaCO3), hardness (550 mg/L as CaCO3), chloride (65 mg/L), and barium (240 ug/L) that are high for water from the fluvial deposits. (USGS)

  17. 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.

  18. 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.

  19. 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.

  20. Crystal structure, thermochromic and magnetic properties of organic-inorganic hybrid compound: (C7H7N2S)2CuCl4

    Science.gov (United States)

    Vishwakarma, Ashok K.; Kumari, Reema; Ghalsasi, Prasanna S.; Arulsamy, Navamoney

    2017-08-01

    The synthesis, thermal analysis, crystal structure and magnetic properties of (2-aminobenzothiazolium)2CuCl4, organic-inorganic hybrid compound, have been described. The compound crystallizes in the monoclinic space group P21/c with two formula units in a unit cell of dimensions a = 6.9522(4) Å, b = 9.6979(4) Å, c = 13.9633(6) Å, β = 97.849(3)° and volume 930.83(8) Å3 at 150(2) K. The structure consists of isolated nearly square planer [CuC14]2- units, with somewhat longer than normal Cusbnd Cl bond lengths [Cusbnd Cl (average) = 2.2711 Å]. The magnetic measurements of (2-aminobenzothiazolium)2CuCl4 using SQUID magnetometer show paramagnetic nature of the compound. Thermal measurements (TG-DTA and DSC) on this compound showed reversible phase transition at 83 °C. This transition is accompanied by the reversible change in colour of the prismatic crystal from green to dark brown, thermochromic behaviour. Temperature dependent EPR measurements on powdered sample ascertain change in coordination sphere around Cu(II) with shift in g|| = 2.150 and g⊥ = 2.071 at room temperature, typical of square planar, to g|| = 2.201 and g⊥ = 2.182 at 170 °C, typical of distorted tetrahedral geometry.

  1. Organic and inorganic compounds in the water streams of the paper machine; Haitta-ainevirrat ja -tasot paperikoneella - PMST 01

    Energy Technology Data Exchange (ETDEWEB)

    Tervonen, P.; Edelmann, K.; Kaijaluoto, S. [VTT Energy, Jyvaeskylae (Finland)

    1998-12-31

    The tightening standards for environmental protection set forth in legislation and the green consideration has reduced the environmental load of the paper and pulp industry significantly during recent years. Paper mills have decreased their water consumption by increasing internal circulation and by improving external effluent treatment. The consequence is that the concentrations of organic and inorganic dissolved and colloidal substances in the paper mill waters have risen. The fresh water consumption of paper machine can be decreased by cleaning the different water streams from the wire- and press-section and by lowering the amount of organic and inorganic materials led to paper machine water. In this case also water from mechanical pulping process and pulp itself should be cleaned. In this project the water use of modern paper machine and stream connections are studied. In addition flows, interactions and retention of dissolved and colloidal materials in the wet end of the paper machine are investigated. By utilizing this knowledge accurate simulation models of paper machine wet end can be created. With this model the various methods and technologies for controlling the harmful components in paper machine wet end are analyzed. (orig.)

  2. Seasonal and diurnal characteristics of water soluble inorganic compounds in the gas and aerosol phase in the Zurich area

    Directory of Open Access Journals (Sweden)

    R. Fisseha

    2006-01-01

    Full Text Available Gas and aerosol samples were taken using a wet effluent diffusion denuder/aerosol collector (WEDD/AC coupled to ion chromatography (IC in the city of Zurich, Switzerland from August to September 2002 and in March 2003. Major water soluble inorganic ions; nitrate, sulfate, and nitrite were analyzed online with a time resolution of two hours for the gas and aerosol phase. The fraction of water soluble inorganic anions in PM10 varied from 15% in August to about 38% in March. Seasonal and diurnal variations of nitrate in the gas and aerosol phase were observed with more than 50% of the total nitrate in the gas phase during August and more than 80% of nitrate in the aerosol phase during March exceeding the concentration of sulfate by a factor of 2. Aerosol sulfate, on the other hand, did not show significant variability with season. However, in the gas phase, the SO2 concentration was 6.5 times higher in winter than in summer. Nitrous acid (HONO also showed a diurnal variation in both the gas and aerosol phase with the lowest concentration (0.2–0.6 µg/m3 in the afternoon. The primary pollutants, NO, CO and SO2 mixing ratios were often at their highest between 04:00–10:00 local time due to the build up of fresh vehicle emission under a nocturnal inversion.

  3. Elaboration, structural, spectroscopy, DSC investigations and Hirshfeld surface analysis of a one-dimensional self-assembled organic-inorganic hybrid compound

    Science.gov (United States)

    Mesbeh, Radhia; Hamdi, Besma; Zouari, Ridha

    2017-01-01

    The new organic-inorganic hybrid of the formula [H2mela]Cu2Cl6, where mela = 1,3,5-triazine-2,4,6-triamine, has been synthesized by the reaction of 1,3,5-triazine-2,4,6-triamine and copper(II) chloride dihydrate in the presence of hydrochloric acid. This compound has been determined by X-ray diffraction analysis and characterized by FT-IR, Raman, NMR characterization, differential scanning calorimetric (DSC) analysis, dielectric measurements and Hirshfeld surface. 1,3,5-triazinidium-2,4,6-triamine hexachlorodicuprate(II) crystallizes in the monoclinic system with space group P21/c. The final refinement of the structure of the program led to the reliability factors unweighted R1 = 3.53% and weighted WR2 = 8.87%. The observed internal C3sbnd N31sbnd C1 and C3sbnd N23sbnd C2 angle (121.5 and 121.4°) at protanated N-atom are significantly greater the other ring angle C1sbnd N12sbnd C2 (117.1°). The titled compound crystallizes as an organic-inorganic one-dimensional (1D) structure. The crystal structure was stabilized by two types of hydrogen bonding Nsbnd H⋯Cl and Nsbnd H⋯N. The infrared spectra was recorded in the 4000-400 cm-1 frequency region and the Raman spectra was recorded in the external region of the anionic sublattice vibration 4000-50 cm-1 at room temperature. Solid-state 13C and 63Cu MAS-NMR spectroscopies are in agreement with the X-ray structure. The differential scanning calorimetric (DSC) show the presence of a structural phase transition of the title compound at 338 K. Hirshfeld surface analyses for visually analyzing intermolecular interactions in crystal structures employing molecular surface contours and 2D fingerprint plots have been used to examine molecular shapes.

  4. Phase transitions and dielectric properties of a hexagonal ABX3 perovskite-type organic-inorganic hybrid compound: [C3H4NS][CdBr3].

    Science.gov (United States)

    Liao, Wei-Qiang; Ye, Heng-Yun; Zhang, Yi; Xiong, Ren-Gen

    2015-06-21

    A new organic-inorganic hexagonal perovskite-type compound with the formula ABX3, thiazolium tribromocadmate(ii) (1), in which thiazolium cations are situated in the space between the one-dimensional chains of face-sharing CdBr(6) octahedra, has been successfully synthesized. Systematic characterizations including differential scanning calorimetry measurements, variable-temperature structural analyses, and dielectric measurements reveal that it undergoes two structural phase transitions, at 180 and 146 K. These phase transitions are accompanied by remarkable dielectric relaxation and anisotropy. The thiazolium cations remain orientationally disordered during the two phase transition processes. The origins of the phase transitions at 180 and 146 K are ascribed to the slowing down and reorientation of the molecular motions of the cations, respectively. Moreover, the dielectric relaxation process well described by the Cole-Cole equation and the prominent dielectric anisotropy are also connected with the dynamics of the dipolar thiazolium cations.

  5. Reduction of organic and inorganic selenium compounds by the edible medicinal basidiomycete Lentinula edodes and the accumulation of elemental selenium nanoparticles in its mycelium.

    Science.gov (United States)

    Vetchinkina, Elena; Loshchinina, Ekaterina; Kursky, Viktor; Nikitina, Valentina

    2013-12-01

    We report for the first time that the medicinal basidiomycete Lentinula edodes can reduce selenium from inorganic sodium selenite (Se(IV)) and the organoselenium compound 1,5-diphenyl-3-selenopentanedione-1,5 (DAPS-25) to the elemental state, forming spherical nanoparticles. Submerged cultivation of the fungus with sodium selenite or with DAPS-25 produced an intense red coloration of L. edodes mycelial hyphae, indicating accumulation of elemental selenium (Se(0)) in a red modification. Several methods, including transmission electron microscopy (TEM), electron energy loss spectroscopy (EELS), and X-ray fluorescence, were used to show that red Se(0) accumulated intracellularly in the fungal hyphae as electron-dense nanoparticles with a diameter of 180.51±16.82 nm. Under designated cultivation conditions, shiitake did not reduce selenium from sodium selenate (Se(VI)).

  6. Characterization of organic-inorganic hybrid layered perovskite and intercalated compound (n-C12H25NH3)2ZnCl4

    Science.gov (United States)

    Abdel-Kader, M. M.; Aboud, A. I.; Gamal, W. M.

    2016-05-01

    We report on some electrical properties and solid-solid phase transitions of organic-inorganic hybrid layered halide perovskite and intercalated compound (n-C12H25NH3)2ZnCl4 which is one member of the long-chain compounds of the series (n-CnH2n+1NH3)2,(n = 8-18). The complex dielectric permittivity ɛ*(ω,T) and the ac conductivity σ (ω,T) were measured as functions of temperature 100 K phase transition at T ≈ (362 ± 2) K, where the compound changes its state from intercalation to non-intercalation with a drastic increase in the c-axis by about 16.4%. The behavior of the frequency-dependent conductivity follows the Jonscher universal power law: σ (ω, T) αῳs(ῳ,T). The mechanism of electrical conduction in the low-temperature phase (phase II) can be described as quantum mechanical tunneling model.

  7. Effects of inhibitors and NaCl on the oxidation of reduced inorganic sulfur compounds by a marine acidophilic, sulfur-oxidizing bacterium, Acidithiobacillus thiooxidans strain SH.

    Science.gov (United States)

    Kamimura, Kazuo; Higashino, Emi; Kanao, Tadayoshi; Sugio, Tsuyoshi

    2005-02-01

    The effect of NaCl and the pathways of the oxidation of reduced inorganic sulfur compounds were studied using resting cells and cell-free extracts of Acidithiobacillus thiooxidans strain SH. This isolate specifically requires NaCl for growth. The oxidation of sulfur and sulfite by resting cells was strongly inhibited by 2-heptyl-4-hydroxyquinoline-N-oxide. Carbonylcyanide m-chlorophenyl-hydrazone and monensin were also relatively strong inhibitors. Thiosulfate-oxidizing activity was not inhibited by these uncouplers. Valinomycin did not inhibit the oxidation of sulfur compounds. NaCl stimulated the sulfur- and sulfite-oxidizing activities in resting cells but not in cell-free extracts. The tetrathionate-oxidizing activity in resting cells was slightly stimulated by NaCl, whereas it did not influence the thiosulfate-oxidizing activity. Sulfide oxidation was biphasic, suggesting the formation of intermediate sulfur. The initial phase of sulfide oxidation was not affected by NaCl, whereas the subsequent oxidation of sulfur in the second phase was Na+-dependent. A model is proposed for the role of NaCl in the metabolism of reduced sulfur compounds in A. thiooxidans strain SH.

  8. Search for organic and volatile inorganic compounds in two surface samples from the Chryse Planitia region of Mars

    Science.gov (United States)

    Biemann, K.; Oro, J.; Toulmin, P., III; Orgel, L. E.; Nier, A. O.; Anderson, D. M.; Flory, D.; Diaz, A. V.; Rushneck, D. R.; Simmonds, P. G.

    1976-01-01

    Two surface samples collected from the Chryse Planitia region of Mars were heated to temperatures up to 500 C, and the volatiles that they evolved were analyzed with a gas chromatograph-mass spectrometer. Only water and carbon dioxide were detected. This implies that organic compounds have not accumulated to the extent that individual components could be detected at levels of a few parts per billion by weight in the samples. Proposed mechanisms for the accumulation and destruction of organic compounds are discussed in the light of this limit.

  9. Vibration in metal and non-metal incubators.

    Science.gov (United States)

    Youngblut, J M; Lewandowski, W; Casper, G R; Youngblut, W R

    1994-01-01

    The purpose of this study was to determine the amount of vibration transmitted to the surface of an incubator mattress. Empty incubators with metal (n = 12) and non-metal (n = 12) bases were monitored for vibration levels when the incubators were turned "off" and when they were turned "on." High levels of low-frequency vibration were detected in both types of incubators in both conditions. The metal incubators transmitted significantly less vibration to the mattress than did the non-metal incubators at several frequencies in the "off," the "on," and the "adjusted" conditions. These results suggest that infants experience significant whole-body vibration while lying in incubators.

  10. Non-metallic inclusions in high manganese austenitic alloys

    OpenAIRE

    A. Grajcar; L. Bulkowski; U. Galisz

    2011-01-01

    Purpose: The aim of the paper is to identify the type, fraction and chemical composition of non-metallic inclusions modified by rare-earth elements in an advanced group of high-manganese austenitic C-Mn-Si-Al-type steels with Nb and Ti microadditions.Design/methodology/approach: The heats of 3 high-Mn steels of a various content of Si, Al and Ti were melted in a vacuum induction furnace and a modification of non-metallic inclusions was carried out by the mischmetal in the amount of 0.87 g or ...

  11. Evans-Showell-Type Polyoxometalates Constructing High-Dimensional Inorganic-Organic Hybrid Compounds with Copper-Organic Coordination Complexes: Synthesis and Oxidation Catalysis.

    Science.gov (United States)

    An, Haiyan; Hou, Yujiao; Wang, Lin; Zhang, Yumeng; Yang, Wei; Chang, ShenZhen

    2017-10-02

    Four new hybrid architectures containing a [Co2Mo10H4O38](6-) polyoxoanion, (en)[Cu3(ptz)4(H2O)4][Co2Mo10H4O38]·24H2O (1), (Hbim)2[{Cu(bim)2(H2O)2}2{Co2Mo10H4O38}]·5H2O (2), H2[Cu(dpdo)3(H2O)4][{Cu2(dpdo)3(H2O)4(CH3CN)}2{Co2Mo10H4O38}2]·9H2O (3), and (H2bpp)4[{Cu(H2O)2}{NaCo2Mo10H4O38}2]·10H2O (4), where ptz = 5-(4-pyridyl)-1H-tetrazole, en = ethylenediamine, bim = benzimidazole, dpdo = 4,4'-bipyridine-N,N'-dioxide, and bpp = 1,3-bis(4-pyridyl)propane, have been prepared and characterized through elemental analysis, thermogravimetric analysis, IR spectroscopy, and powder and single-crystal X-ray diffraction. Compound 1 shows a 3D host-guest framework composed of 3D Cu-ptz as the host and Evans-Showell-type polyoxoanion [Co2Mo10H4O38](6-) as the guest. Compound 2 is constructed from [Co2Mo10H4O38](6-) polyoxoanions and Cu-bim coordination complexes to form a 2D covalent layer. Compound 3 also exhibits a 2D hybrid network based on [Co2Mo10H4O38](6-) polyoxoanions linked by Cu-dpdo coordination groups. Compound 4 is a 1D double-chain structure composed of [Co2Mo10H4O38](6-) polyoxoanions joined together by Na(+) and Cu(2+) cations. As far as we know, compound 1 is the first host-guest compound with an Evans-Showell-type polyoxometalate as the guest, and compounds 2 and 3 are the first 2D inorganic-organic hybrid architectures constructed from Evans-Showell-type polyoxometalates. Compounds 1-4 are redox catalysts that heterogeneously prompt sulfide and alcohol oxidation with excellent efficiency.

  12. Preparation a new sorbent based on polymeric ionic liquid for stir cake sorptive extraction of organic compounds and inorganic anions.

    Science.gov (United States)

    Huang, Xiaojia; Wang, Yulei; Hong, Qiuyun; Liu, Yi; Yuan, Dongxing

    2013-11-01

    A new multi-interaction sorbent (MIS) based on polymeric ionic liquid was prepared and used as extractive medium of stir cake sorptive extraction (SCSE). In the presence of dimethyl sulfoxide, an ionic liquid, 1-vinylbenzyl-3-methylimidazolium chloride was used as monomer to copolymerize in situ with divinylbenzene to form the MIS. The influences of the content of monomer and the porogen solvent in the polymerization mixture on the extraction performance were investigated thoroughly. The MIS was characterized by infrared spectroscopy, elemental analysis, scanning electron microscopy and mercury intrusion porosimetry. Parabens and aromatic amines were used to investigate the extraction performance of MIS-SCSE for apolar and strongly polar analytes, respectively. The extraction parameters for parabens and aromatic amines were optimized. At the same time, simple and sensitive analytical methods for parabens and aromatic amines in real samples were developed by the combination of MIS-SCSE and HPLC/DAD. Some inorganic anions, such as F(-), Br(-), NO3(-), PO4(3-) and SO4(2-), were used to test the extraction performance of MIS-SCSE for anions. Results indicated that mechanism involved in the extraction of MIS is the multi-interaction modes including π-π, hydrophobic, hydrogen-bonding, dipole-dipole and anion-exchange interactions.

  13. Compilation and evaluation of gas phase diffusion coefficients of reactive trace gases in the atmosphere: volume 1. Inorganic compounds

    Science.gov (United States)

    Tang, M. J.; Cox, R. A.; Kalberer, M.

    2014-09-01

    Diffusion of gas molecules to the surface is the first step for all gas-surface reactions. Gas phase diffusion can influence and sometimes even limit the overall rates of these reactions; however, there is no database of the gas phase diffusion coefficients of atmospheric reactive trace gases. Here we compile and evaluate, for the first time, the diffusivities (pressure-independent diffusion coefficients) of atmospheric inorganic reactive trace gases reported in the literature. The measured diffusivities are then compared with estimated values using a semi-empirical method developed by Fuller et al. (1966). The diffusivities estimated using Fuller's method are typically found to be in good agreement with the measured values within ±30%, and therefore Fuller's method can be used to estimate the diffusivities of trace gases for which experimental data are not available. The two experimental methods used in the atmospheric chemistry community to measure the gas phase diffusion coefficients are also discussed. A different version of this compilation/evaluation, which will be updated when new data become available, is uploaded online (google.com/site/mingjintang/home/diffusion"target="_blank">https://sites.google.com/site/mingjintang/home/diffusion).

  14. Vibrational spectroscopic and DFT calculation studies of a new organic-inorganic compound of bis (4-acetylanilinium) tetrachlorocadmiate (II)

    Science.gov (United States)

    Jellibi, A.; Chaabane, I.; Guidara, K.

    2016-10-01

    The FT-IR and Raman vibrational spectra of bis (4-acetylanilinium) tetrachlorocadmiate (II) compound have been measured at room temperature by FT-infrared spectroscopy (4000-400 cm-1) on polycrystalline samples, and by Raman spectroscopy (3600-30 cm-1) on monocrystals. The structure of the [C8H10NO] 2CdCl4 formed by two cations [C8H10NO]+ of same type and one type of anion [CdCl4]2- was optimized by density functional theory (DFT) using the B3LYP method. The theoretical wavenumbers spectra were scaled by multiple scaling factors, yielding a good agreement between the experimentally recorded and the theoretically calculated values. Root mean square (rms) value was calculated and the small difference between experimental and calculated modes has been interpreted by intermolecular interactions in the crystal. The comparison between the [C8H9NO] ligand and the [C8H10NO]2[CdCl4] compound of the Raman spectra showed a decrease in the wavenumber of the bands assigned to the stretching vibration of (NH3) group in the compound due to the effect of the protonation of the nitrogen.

  15. Interaction mechanism of non-metallic particles with crystallization front

    Directory of Open Access Journals (Sweden)

    Żak P. L.

    2017-03-01

    Full Text Available The process of steel solidification in the CCS mould is accompanied by a number of phenomena relating to the formation of non-metallic phase, as well as the mechanism of its interaction with the existing precipitations and the advancing crystallization front. In the solidification process the non-metallic inclusions may be absorbed or repelled by the moving front. As a result a specific distribution of non-metallic inclusions is obtained in the solidified ingot, and their distribution is a consequence of these processes. The interaction of a non-metallic inclusion with the solidification front was analyzed for alumina, for different values of the particle radius. The simulation was performed with the use of own computer program. Each time a balance of forces acting on a particle in its specific position was calculated. On this basis the change of position of alumina particle in relation to the front was defined for a specific radius and original location of the particle with respect to the front.

  16. Oxidative treatment of bromide-containing waters: formation of bromine and its reactions with inorganic and organic compounds--a critical review.

    Science.gov (United States)

    Heeb, Michèle B; Criquet, Justine; Zimmermann-Steffens, Saskia G; von Gunten, Urs

    2014-01-01

    Bromide (Br(-)) is present in all water sources at concentrations ranging from ≈ 10 to >1000 μg L(-1) in fresh waters and about 67 mg L(-1) in seawater. During oxidative water treatment bromide is oxidized to hypobromous acid/hypobromite (HOBr/OBr(-)) and other bromine species. A systematic and critical literature review has been conducted on the reactivity of HOBr/OBr(-) and other bromine species with inorganic and organic compounds, including micropollutants. The speciation of bromine in the absence and presence of chloride and chlorine has been calculated and it could be shown that HOBr/OBr(-) are the dominant species in fresh waters. In ocean waters, other bromine species such as Br2, BrCl, and Br2O gain importance and may have to be considered under certain conditions. HOBr reacts fast with many inorganic compounds such as ammonia, iodide, sulfite, nitrite, cyanide and thiocyanide with apparent second-order rate constants in the order of 10(4)-10(9)M(-1)s(-1) at pH 7. No rate constants for the reactions with Fe(II) and As(III) are available. Mn(II) oxidation by bromine is controlled by a Mn(III,IV) oxide-catalyzed process involving Br2O and BrCl. Bromine shows a very high reactivity toward phenolic groups (apparent second-order rate constants kapp ≈ 10(3)-10(5)M(-1)s(-1) at pH 7), amines and sulfamides (kapp ≈ 10(5)-10(6)M(-1)s(-1) at pH 7) and S-containing compounds (kapp ≈ 10(5)-10(7)M(-1)s(-1) at pH 7). For phenolic moieties, it is possible to derive second-order rate constants with a Hammett-σ-based QSAR approach with [Formula in text]. A negative slope is typical for electrophilic substitution reactions. In general, kapp of bromine reactions at pH 7 are up to three orders of magnitude greater than for chlorine. In the case of amines, these rate constants are even higher than for ozone. Model calculations show that depending on the bromide concentration and the pH, the high reactivity of bromine may outweigh the reactions of chlorine during

  17. Crystal structures and spectral properties of two polyoxometalate-based inorganic-organic compounds from silver-azine building blocks with bis-bidentate and tridentate ligands

    Science.gov (United States)

    An, Bing; Zhou, Rui-Min; Sun, Li; Bai, Yan; Dang, Dong-Bin

    2014-07-01

    Two polyoxometalate-based inorganic-organic hybrid compounds constructed from silver(I)-L species and saturated Keggin type polyoxoanion, [Ag2L21]2(SiMo12O40)·1.5DMF·0.5CH3OHṡH2O 1 and [{Ag4L22(DMF)5}(SiMo12O40)] 2 (L1 = phenyl 2-pyridyl ketone azine, L2 = 3-phenyltriazolo[1,5-a]pyridine), have been synthesized and structurally characterized by IR, UV, elemental analysis, XRPD and complete single crystal structure analyses, where the ligands L1 and L2 are bis-bidentate and tridentate azines synthesized with the same materials under different conditions. The structure of 1 exhibits a dinuclear double-helicate with [SiMo12O40]4- anions as counter ions, where all of the Ag centers coordinate to bis-bidentate chelating ligands. Compound 2 displays a two-dimensional sheet formed by the Ag-organic infinite chains and the [SiMo12O40]4- alternately arranged in a “rail-like” fashion. The luminescent properties of 1 and 2 in the solid state were investigated.

  18. Crystal structures and spectral properties of two polyoxometalate-based inorganic-organic compounds from silver-azine building blocks with bis-bidentate and tridentate ligands.

    Science.gov (United States)

    An, Bing; Zhou, Rui-Min; Sun, Li; Bai, Yan; Dang, Dong-Bin

    2014-07-15

    Two polyoxometalate-based inorganic-organic hybrid compounds constructed from silver(I)-L species and saturated Keggin type polyoxoanion, [Ag2L2(1)]2(SiMo12O40)·1.5DMF·0.5CH3OH⋅H2O 1 and [{Ag4L2(2)(DMF)5}(SiMo12O40)] 2 (L(1) = phenyl 2-pyridyl ketone azine, L(2) = 3-phenyltriazolo[1,5-a]pyridine), have been synthesized and structurally characterized by IR, UV, elemental analysis, XRPD and complete single crystal structure analyses, where the ligands L(1) and L(2) are bis-bidentate and tridentate azines synthesized with the same materials under different conditions. The structure of 1 exhibits a dinuclear double-helicate with [SiMo12O40](4)(-) anions as counter ions, where all of the Ag centers coordinate to bis-bidentate chelating ligands. Compound 2 displays a two-dimensional sheet formed by the Ag-organic infinite chains and the [SiMo12O40](4)(-) alternately arranged in a "rail-like" fashion. The luminescent properties of 1 and 2 in the solid state were investigated. Copyright © 2014 Elsevier B.V. All rights reserved.

  19. Data-driven signal-resolving approaches of infrared spectra to explore the macroscopic and microscopic spatial distribution of organic and inorganic compounds in plant.

    Science.gov (United States)

    Chen, Jian-bo; Sun, Su-qin; Zhou, Qun

    2015-07-01

    The nondestructive and label-free infrared (IR) spectroscopy is a direct tool to characterize the spatial distribution of organic and inorganic compounds in plant. Since plant samples are usually complex mixtures, signal-resolving methods are necessary to find the spectral features of compounds of interest in the signal-overlapped IR spectra. In this research, two approaches using existing data-driven signal-resolving methods are proposed to interpret the IR spectra of plant samples. If the number of spectra is small, "tri-step identification" can enhance the spectral resolution to separate and identify the overlapped bands. First, the envelope bands of the original spectrum are interpreted according to the spectra-structure correlations. Then the spectrum is differentiated to resolve the underlying peaks in each envelope band. Finally, two-dimensional correlation spectroscopy is used to enhance the spectral resolution further. For a large number of spectra, "tri-step decomposition" can resolve the spectra by multivariate methods to obtain the structural and semi-quantitative information about the chemical components. Principal component analysis is used first to explore the existing signal types without any prior knowledge. Then the spectra are decomposed by self-modeling curve resolution methods to estimate the spectra and contents of significant chemical components. At last, targeted methods such as partial least squares target can explore the content profiles of specific components sensitively. As an example, the macroscopic and microscopic distribution of eugenol and calcium oxalate in the bud of clove is studied.

  20. Formation of inorganic nanofibers by heat-treatment of poly(vinyl alcohol-zirconium compound hybrid nanofibers

    Directory of Open Access Journals (Sweden)

    Nakane K.

    2013-01-01

    Full Text Available Poly(vinyl alcohol-zirconium compound hybrid nanofibers (precursors were formed by electrospinning employing water as a solvent for the spinning solution. The precursors were converted into oxide (ZrO2, carbide (ZrC or nitride (ZrN nanofibers by heating them in air, Ar or N2 atmospheres. Monoclinic ZrO2 nanofibers with high-specific surface area were obtained by heat-treatment of the precursors in air. ZrC and ZrN nanofibers could be obtained below theoretical temperatures calculated from thermodynamics data.

  1. Polyoxometalate-based organic-inorganic hybrid compounds containing transition metal mixed-organic-ligand complexes of N-containing and pyridinecarboxylate ligands.

    Science.gov (United States)

    Zhao, De-Chuan; Hu, Yang-Yang; Ding, Hong; Guo, Hai-Yang; Cui, Xiao-Bing; Zhang, Xiao; Huo, Qi-Sheng; Xu, Ji-Qing

    2015-05-21

    Five new organic–inorganic hybrid compounds based on the Keggin-type polyoxoanion [SiW12O40]4−, namely [Cu3(2,2′-bpy)3(inic)(μ2-OH)(H2O)][SiW12O40]·2H2O (1), [Cu6(phen)6(μ3-Cl)2(μ2-Cl)2Cl2(inic)2][SiW12O40]·6H2O (2), [Cu2(hnic)(2,2′-bpy)2Cl]2[H2SiW12O40] (3), [Cu2(nic)(phen)2Cl2]2[SiW12O40] (4) and [Cu2(pic)(2,2′-bpy)2Cl]2[SiW12O40] (5) (inic = isonicotinic acid, hnic = 2-hydroxy-nicotinic acid, nic = nicotinic acid, pic = picolinic acid, 2,2′-bpy = 2,2′-bipyridine, phen = 1,10-phenanthroline) have been synthesized and characterized by IR, UV-Vis, XPS, XRD, cyclic voltammetric measurements, photoluminescence analysis and single crystal X-ray diffraction analysis. Crystal analysis reveals that compound 1 exhibits a 2-D double layered framework structure constructed from [SiW12O40]4− and copper-aqua-2,2′-bipy-hydroxyl-isonicotinate complexes. Compound 2 is a 0-D discrete structure formed by [SiW12O40]4− and copper-chloro-isonicotinate-phenanthroline complexes. Compound 3 shows a 1-D single chain structure based on the linkage of copper-2,2-bpy-chloro-2-hydroxy-nicotinate complexes and [SiW12O40]4−. Compounds 4 and 5 both contain polyoxometalate supported transition metal complexes, one is a polyoxometalate supported copper-chloro-nicotinate-phenanthroline complex in 4, and the other is a polyoxometalate supported copper-2,2-bpy-chloro-nicotinate complex in 5. It should be noted that nicotinic, isonicotinic and picolinic acids are structural isomers and 2-hydroxy-nicotinic acid is an in situ hydroxylated product of nicotinic acid. In addition, photocatalytic degradation of Rhodamine B (RhB) by compounds 1–5 has been investigated in aqueous solutions.

  2. Stand-off Raman spectroscopy: a powerful technique for qualitative and quantitative analysis of inorganic and organic compounds including explosives.

    Science.gov (United States)

    Zachhuber, Bernhard; Ramer, Georg; Hobro, Alison; Chrysostom, Engelene T H; Lendl, Bernhard

    2011-06-01

    A pulsed stand-off Raman system has been built and optimised for the qualitative and quantitative analysis of inorganic and organic samples including explosives. The system consists of a frequency doubled Q-switched Nd:YAG laser (532 nm, 10 Hz, 4.4 ns pulse length), aligned coaxially with a 6″ Schmidt-Cassegrain telescope for the collection of Raman scattered light. The telescope was coupled via a fibre optic bundle to an Acton standard series SP-2750 spectrograph with a PI-MAX 1024RB intensified CCD camera equipped with a 500-ps gating option for detection. Gating proved to be essential for achieving high signal-to-noise ratios in the recorded stand-off Raman spectra. In some cases, gating also allowed suppression of disturbing fluorescence signals. For the first time, quantitative analysis of stand-off Raman spectra was performed using both univariate and multivariate methods of data analysis. To correct for possible variation in instrumental parameters, the nitrogen band of ambient air was used as an internal standard. For the univariate method, stand-off Raman spectra obtained at a distance of 9 m on sodium chloride pellets containing varying amounts of ammonium nitrate (0-100%) were used. For the multivariate quantification of ternary xylene mixtures (0-100%), stand-off spectra at a distance of 5 m were used. The univariate calibration of ammonium nitrate yielded R (2) values of 0.992, and the multivariate quantitative analysis yielded root mean square errors of prediction of 2.26%, 1.97% and 1.07% for o-, m- and p-xylene, respectively. Stand-off Raman spectra obtained at a distance of 10 m yielded a detection limit of 174 μg for NaClO(3). Furthermore, to assess the applicability of stand-off Raman spectroscopy for explosives detection in "real-world" scenarios, their detection on different background materials (nylon, polyethylene and part of a car body) and in the presence of interferents (motor oil, fuel oil and soap) at a distance of 20 m was also

  3. Seasonal variation and source apportionment of organic and inorganic compounds in PM2.5 and PM10 particulates in Beijing, China

    Institute of Scientific and Technical Information of China (English)

    Xingru Li; Yuesi Wang; Xueqing Guo; Yingfeng Wang

    2013-01-01

    The distribution and source of the solvent-extractable organic and inorganic components in PM2.5 (aerodynamics equivalent diameter below 2.5 microns),and PM10 (aerodynamics equivalent diameter below 10 microns) fractions of airborne particles were studied weekly from September 2006 to August 2007 in Beijing.The extracted organic and inorganic compounds identified in both particle size ranges consisted of n-alkanes,PAHs (polycyclic aromatic hydrocarbons),fatty acids and water soluble ions.The potential emission sources of these organic compounds were reconciled by combining the values of n-alkane carbon preference index (CPI),%waxCn,selected diagnostic ratios of PAHs and principal component analysis in both size ranges.The mean cumulative concentrations of n-alkanes reached 1128.65 ng/m3 in Beijing,74% of which (i.e.,831.7 ng/m3) was in the PM2.5 fraction,PAHs reached 136.45 ng/m3 (113.44 ng/m3 or 83% in PM2.5),and fatty acids reached 436.99 ng/m3 (324.41 ng/m3 or 74% in PM2.5),which resulted in overall enrichment in the fine particles.The average concentrations of SO42-,NO3-,and NH4+ were 21.3 ± 15.2,6.1 ± 1.8,12.5 ± 6.1 μg/m3 in PM2.5,and 25.8 ± 15.5,8.9 ± 2.6,16.9 ± 9.5 μg/m3 in PM10,respectively.These three secondary ions primarily existed as ammonium sulfate ((NH4)2SO4),ammonium bisulfate (NH4HSO4) and ammonium nitrate (NH4NO3).The characteristic ratios of PAHs revealed that the primary sources of PAHs were coal combustion,followed by gasoline combustion.The ratios of stearic/palmitic acid indicated the major contribution of vehicle emissions to fatty acids in airborne particles.The major alkane sources were biogenic sources and fossil fuel combustion.The major sources of PAHs were vehicular emission and coal combustion.

  4. Seasonal variation and source apportionment of organic and inorganic compounds in PM2.5 and PM10 particulates in Beijing, China.

    Science.gov (United States)

    Li, Xingru; Wang, Yuesi; Guo, Xueqing; Wang, Yingfeng

    2013-04-01

    The distribution and source of the solvent-extractable organic and inorganic components in PM2.5 (aerodynamics equivalent diameter below 2.5 microns), and PM10 (aerodynamics equivalent diameter below 10 microns) fractions of airborne particles were studied weekly from September 2006 to August 2007 in Beijing. The extracted organic and inorganic compounds identified in both particle size ranges consisted of n-alkanes, PAHs (polycyclic aromatic hydrocarbons), fatty acids and water soluble ions. The potential emission sources of these organic compounds were reconciled by combining the values of n-alkane carbon preference index (CPI), %waxC(n), selected diagnostic ratios of PAHs and principal component analysis in both size ranges. The mean cumulative concentrations of n-alkanes reached 1128.65 ng/m3 in Beijing, 74% of which (i.e., 831.7 ng/m3) was in the PM2.5 fraction, PAHs reached 136.45 ng/m3 (113.44 ng/m3 or 83% in PM2.5), and fatty acids reached 436.99 ng/m3 (324.41 ng/m3 or 74% in PM2.5), which resulted in overall enrichment in the fine particles. The average concentrations of SO4(2-), NO3(-), and NH4(+) were 21.3 +/- 15.2, 6.1 +/- 1.8, 12.5 +/- 6.1 microg/m3 in PM2.5, and 25.8 +/- 15.5, 8.9 +/- 2.6, 16.9 +/- 9.5 microg/m3 in PM10, respectively. These three secondary ions primarily existed as ammonium sulfate ((NH4)2SO4), ammonium bisulfate (NH4HSO4) and ammonium nitrate (NH4NO3). The characteristic ratios of PAHs revealed that the primary sources of PAHs were coal combustion, followed by gasoline combustion. The ratios of stearic/palmitic acid indicated the major contribution of vehicle emissions to fatty acids in airborne particles. The major alkane sources were biogenic sources and fossil fuel combustion. The major sources of PAHs were vehicular emission and coal combustion.

  5. Trends in air concentration and deposition at background monitoring sites in Sweden - major inorganic compounds, heavy metals and ozone

    Energy Technology Data Exchange (ETDEWEB)

    Kindbom, K.; Svensson, Annika; Sjoeberg, K.; Pihl Karlsson, G.

    2001-09-01

    This report describes concentrations in air of sulphur compounds, soot, nitrogen compounds and ozone in Sweden between 1985-1998. Time trends of concentration in precipitation and deposition of sulphate, nitrate, ammonium, acidity, base cations and chloride in six different regions covering Sweden are evaluated during the period 1983-1998. Trends of heavy metals in precipitation have been analysed for the period 1983-1998 and the change in heavy metal concentration, 1975-1995, in mosses is described. Data used in the trend analyses originates from measurements performed at six Swedish EMEP stations and from approximately 25 stations within the national Precipitation Chemistry Network. Two different statistical methods, linear regression and the non-parametric Mann Kendall test, have been used to evaluate changes in annual mean values. Time trends of concentration of sulphur dioxide, particulate sulphate, soot, nitrogen dioxide, total nitrate and total ammonium in air show highly significant decreasing trends, except for soot at one station in northern Sweden. Concentrations of ozone have a strong seasonal variation with a peak occurring in spring every year. However, annual ozone concentrations show no obvious trends in spite of decreasing emissions of the precursors NOx and VOC. A slight indication of a decreasing trend in the number of ozone episodes might be seen from 1990 to 1998. Sulphate concentrations in precipitation and deposition show strongly significant decreasing trends in the whole country. Concentrations and deposition of nitrate and ammonium have been decreasing in all areas except for nitrate at stations in south-west and north-west Sweden and ammonium in south-west Sweden. Acidity has decreased in all areas since 1989, resulting in increasing pH values in Sweden. The interannual variations of concentration and deposition of base cations and chloride are large and few general trends can be seen during 1983-1997. Time trends of four heavy metals in

  6. A study on non-metallic structure of heliostat

    Energy Technology Data Exchange (ETDEWEB)

    Liu Xiaobin; Zang Chuncheng; Zhang Xiliang; Wang Yangzhong; Du Fengli [Himin Solar Energy Group Co., Ltd, Dezhou City (China); Wang Zhifeng [Inst. of Electrical Engineering, CAS, BJ (China)

    2008-07-01

    Heliostat constitutes a very important component in the solar power tower system. Its importance derives from three aspects: one is the large proportion in the total cost, accounting for about 50% of the whole, the other is its concentration efficiency and reflectivity heavily determining the power conversion from solar thermal energy to electrical energy, another is itself power consumption amount highly expressing failure or success of the power plant. Therefore, serious efforts and considerations from the structure, motion and control mode to material selection have to be given in the design and optimization of heliostat. In the present paper, the mechanical and aging performance of non-metallic materials is investigated and compared. The possibility of these non-metallic materials in the application of heliostat structure is discussed. (orig.)

  7. 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.

  8. 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

  9. Increased Survivorship and Altered Cytokine Profile from Treatment of Influenza A H1N1-Infected Mice with Ekybion: A Drug Complex of Natural Extracts and Inorganic Compounds

    Directory of Open Access Journals (Sweden)

    Christopher Lupfer

    2011-01-01

    Full Text Available Ekybion is a drug complex of 16 natural extracts and inorganic compounds designed to treat a variety of respiratory pathogens of bacterial and viral origin. It is licensed throughout Europe for the treatment of respiratory tract infections from equine parainfluenza type 3 and equine herpes virus type 1 in equine stables. The purpose of this paper was to test the efficacy of Ekybion on a well-developed animal model of influenza A infection and determine a mode of action. Experiments were performed with Balb/c mice infected with a lethal dose of influenza A/PR/8/34 H1N1 virus and treated with nebulized Ekybion every 8 h in a time-dependant or dose-dependant fashion. These experiments showed that mice treated prior to infection with Ekybion had a higher survival rates (~46% compared with untreated animals (~0%. Paradoxically, these mice showed no significant difference in lung virus titer or weight loss. There was, however, a decrease in the level of GM-CSF, IL-6, and G-CSF cytokines in the lungs of Ekybion-treated, infected mice. It is possible that decreases in proinflammatory cytokines may have contributed to increased survivorship in Ekybion-treated influenza-infected mice.

  10. 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.

  11. An iodide-adduct high-resolution time-of-flight chemical-ionization mass spectrometer: application to atmospheric inorganic and organic compounds.

    Science.gov (United States)

    Lee, Ben H; Lopez-Hilfiker, Felipe D; Mohr, Claudia; Kurtén, Theo; Worsnop, Douglas R; Thornton, Joel A

    2014-06-03

    A high-resolution time-of-flight chemical-ionization mass spectrometer (HR-ToF-CIMS) using Iodide-adducts has been characterized and deployed in several laboratory and field studies to measure a suite of organic and inorganic atmospheric species. The large negative mass defect of Iodide, combined with soft ionization and the high mass-accuracy (5500) of the time-of-flight mass spectrometer, provides an additional degree of separation and allows for the determination of elemental compositions for the vast majority of detected ions. Laboratory characterization reveals Iodide-adduct ionization generally exhibits increasing sensitivity toward more polar or acidic volatile organic compounds. Simultaneous retrieval of a wide range of mass-to-charge ratios (m/Q from 25 to 625 Th) at a high frequency (>1 Hz) provides a comprehensive view of atmospheric oxidative chemistry, particularly when sampling rapidly evolving plumes from fast moving platforms like an aircraft. We present the sampling protocol, detection limits and observations from the first aircraft deployment for an instrument of this type, which took place aboard the NOAA WP-3D aircraft during the Southeast Nexus (SENEX) 2013 field campaign.

  12. Hydrothermal Synthesis and Crystal Structure of Inorganic-organic Hybrid Compound [H3NC2H4NH2]VOPO4

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    An inorganic-organic hybrid compound, [H3NC2H4NH2]VOPO4 was synthesized by meansof the hydrothermal method. It was crystallized in a monoclinic system, a space group P21/c,with the crystal cell parameters: a=0. 922 85(11) nm, b=0. 729 94(9) nm, c=0. 984 95(11)nm, β=101. 280(3)°, V=0. 650 67(13) nm3, Mr=223.02 g/mol, Dc=2. 277 g/cm3, Z=4,R= 0. 031 5, ωR= 0. 086 5, GOF = 1. 085. The VO5N octahedra chains are corner-linked byPO4 tetrahedra; the VOsN octahedra are all trans-linked with V-O bonds being alternately short and long. The monoprotonated ethylenediamine was intercalated between the layers with one end coordinating to V and the other end as an H-bond donor interacting with a terminal O atom of PO4 from a neighboring sheet. The elementary analysis, infrared spectrum characters and thermal stability were also given.

  13. Preparation and characteristics of high pH-resistant sol-gel alumina-based hybrid organic-inorganic coating for solid-phase microextraction of polar compounds.

    Science.gov (United States)

    Liu, Mingming; Liu, Ying; Zeng, Zhaorui; Peng, Tianyou

    2006-03-10

    A novel alumina-based hybrid organic-inorganic sol-gel coating was first developed for solid-phase microextraction (SPME) from a highly reactive alkoxide precursor, aluminum sec-butoxide, and a sol-gel-active organic polymer hydroxyl-terminated polydimethylsiloxane (OH-TSO). The underlying mechanism was discussed and confirmed by IR spectra. The porous surface structure of the sol-gel coating was revealed by scanning electron microscopy. A detailed investigation was conducted to evaluate the remarked performance of the newly developed sol-gel alumina-OH-TSO hybrid materials. In stark contrast to the sol-gel silica-based coating, the alumina-based coating demonstrated excellent pH stability. In addition, good thermal resistance and coating preparation reproducibility are also its outstanding performance. As compared to silica-based hybrids material, the ligand exchange ability of alumina makes it structurally superior extraction sorbents for polar compounds, such as fatty acids, phenols, alcohols, aldehydes and amines. Practical applicability of the prepared alumina-OH-TSO fiber was demonstrated through the analysis of volatile alcohols and fatty acids in beer. The recoveries obtained ranged from 85.7 to 104% and the relative standard deviation values for all analytes were below 9%.

  14. Prediction of activity coefficients in liquid aerosol particles containing organic compounds, dissolved inorganic salts, and water—Part 1: Organic compounds and water by consideration of short- and long-range effects using X-UNIFAC.1

    Science.gov (United States)

    Erdakos, Garnet B.; Asher, William E.; Seinfeld, John H.; Pankow, James F.

    The semi-empirical group contribution method (GCM) of Kikic et al. [Chem. Eng. Sci. 46 (1991) 2775-2780] for estimating activity coefficient ( ζ) values of neutral organic compounds and water in solutions composed of organic compounds, dissolved inorganic salts, and water is adapted for application to atmospheric particulate matter (PM). It is assumed that ζ values are determined by a combination of short- and long-range interactions. The ζ expression involves conventional UNIFAC terms and a Debye-Hückel term, with the former computed using group-group interaction parameters. Organic-organic interaction parameters are assigned the values from the UNIFAC-LLE model of Magnussen et al. [Ind. Eng. Chem. Process Design Develop. 20 (1981) 331-339]. Forty interaction parameters (ion-solvent group and anion-cation) were obtained from Kikic et al. [Chem. Eng. Sci. 46 (1991) 2775-2780], Achard et al. [Fluid Phase Equilibria 98 (1994) 71-89], and Ming and Russell [Am. Inst. Chem. Eng. J. 48 (2002) 1331-1348]. Twenty additional interaction parameters (ion-solvent group) are estimated based on 879 UNIQUAC-fitted ζ values for organic compounds and water. The fitted ζ values are based on liquid-liquid equilibrium (LLE) data for a range of ternary and quaternary organic/inorganic salt/water mixtures at 293-308 K. The UNIQUAC fits are analogous to those described by Fredenslund et al. [Vapor-Liquid Equilibria Using UNIFAC: A Group-Contribution Method, Elsevier Scientific Publishing, New York, 1977]. The LLE mixture compositions range from primarily organic solutions to primarily aqueous solutions with maximum ionic strengths of ˜5 mol kg -1. The groups characteristic of organic compounds found in atmospheric PM considered here include: CH 3-, -CH 2-, -CH|-, -C||-, -OH, -CH 2CO-, and -COOH. These are: single bonded carbon with three, two, one, and zero hydrogens, respectively, hydroxyl, -CH 2-carbonyl, and carboxyl, respectively. The inorganic salts represented in the mixture

  15. 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.

  16. Castor Bean Cereal Based Bio-Organic-Inorganic Compound Fertilizers and Use%蓖麻粕基生物有机无机复混肥及其应用

    Institute of Scientific and Technical Information of China (English)

    陈绍荣; 邵建华; 赵立新; 刘园园

    2014-01-01

    A brief account is given of the properties and features of castor bean cereal based bio-organic-inorganic compound fertilizers.By field experiment of fertilizer efficiency with corn, rice and peanut , it is proved that castor bean cereal based bio-organic-inorganic compound fertilizers have better effects on increasing production and improving the properities of soil, and can be widely applied to grain and oil crops.%简要介绍了蓖麻粕基生物有机无机复混肥的性能及特点。通过玉米、水稻、花生大田肥效试验,结果证明蓖麻粕基生物有机无机复混肥具有较好的增产改土效果,可在粮油作物上推广应用。

  17. Hybrid organic PVDF-inorganic M-rGO-TiO2 (M = Ag, Pt) nanocomposites for multifunctional volatile organic compound sensing and photocatalytic degradation-H2 production.

    Science.gov (United States)

    Ong, W L; Gao, M; Ho, G W

    2013-11-21

    This work focused on the development of a hybrid organic-inorganic TiO2 nanocomposite, which demonstrates the first ever report on harmful volatile organic compound (VOC) sensing and photocatalytic degradation-H2 production. The sensing and photocatalytic properties are enhanced by the synergetic effects of well-structured TiO2 nanotubes, metal nanoparticles and reduced graphene oxide loading for enhanced light absorption and charge-transfer kinetics. Hybridization of a functionalized TiO2 nanocomposite with a polyvinylidene fluoride (PVDF) matrix induced strong cross-linking networks between the inorganic-organic components, which promote mechanical reinforcement-flexibility and highly porous asymmetric structures. The developed solution processable nanocomposite has immense potential to remedy the global environmental and energy issues by producing clean water/air and energy from organic compound waste.

  18. Non-metallic Inclusions in Continuously Cast Aluminum Killed Steels

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    In aluminum killed steels, the size, shape, quantity and formation of non-metallic inclusions in ladle steel (before and after RH vacuum treatment) and in tundish as well as in slabs were studied by EPMA (Electron Probe Microanalysis) and by analyzing the total oxygen. The results showed that in the slabs the total oxygen was quite low and the inclusions discovered were mainly small-sized angular alumina inclusions. This indicates that most inclusions have been removed by floating out during the continuous casting process. In addition, the countermeasures were discussed to decrease the alumina inclusions in the slabs further.

  19. Testing theOdour Quality of Non-Metallic Materials

    Directory of Open Access Journals (Sweden)

    AVIJIT SINGH GANGWAR

    2014-10-01

    Full Text Available This report has been compiled on the completion of 3 week summer training at ICAT. It discusses about a very necessary and least popular part of the Automotive Industry i.e. Testing and Certification. It discusses about one of the government notified Testing body ICAT which is one of just 6 such organisations in India.This report deals with the odour quality testing of non-metallic materials that are used for automobile compartment and parts associated with the compartment.

  20. Organic inorganic compound fertilizer application in Wheat Fertilizer Efficiency Experiment of%有机-无机复混肥料在小麦上的应用肥效试验初探

    Institute of Scientific and Technical Information of China (English)

    费秀华

    2012-01-01

      根据观察:在小麦上应用有机无机-复混肥料对小麦生长有促进作用,且无副作用,对小麦生长是安全的。%  according to the observation in wheat: application of organic-inorganic compound fertilizer on wheat growth, promote, and no negative effects on the growth of wheat, is safe.

  1. Synthesis and Characterization of Two Novel Organic-Inorganic Compounds Based on Tetrahexyl and Tetraheptyl Ammonium Ions and the Preyssler Anion and Their Catalytic Activities in the Synthesis of 4-Aminopyrazolo[3,4-d]- Pyrimidines

    Directory of Open Access Journals (Sweden)

    Fatemeh Farrash Bamoharram

    2010-04-01

    Full Text Available Two novel organic–inorganic compounds based on tetrahexylammonium (THA and tetraheptylammonium (THPA ions and the Preyssler anion, [NaP5W30O110]14-, were synthesized and formulated as (THA7.7H6.3 [NaP5W30O110] (A and (THPA7.5 H6.5[N aP5W30O110] (B. The synthesized compounds were characterized by IR, UV, and TGA and used for the catalytic synthesis of 4-aminopyrazolo[3,4,-d]pyrimidine derivatives 2a-2d. Our findings showed efficient catalytic activities for A and B.

  2. Investigation of the influence of liquid water films on O3 and PAN deposition on plant leaf surfaces treated with organic / inorganic compounds

    Science.gov (United States)

    Sun, Shang; Moravek, Alexander; von der Heyden, Lisa; Held, Andreas; Kesselmeier, Jürgen; Sörgel, Matthias

    2016-04-01

    Liquid water films on environmental surfaces play an important role in various fields of interest (Burkhardt and Eiden, 1994). For example, the deposition of water soluble trace gases could be increased by surface moisture. Chameides and Stelson (1992) found out that the dissolution of trace gases in airborne particulate matter increases with rising water/solid ratio of the particles. Further, Flechard et al. (1999) concluded that deliquescent salt particles represent a potential sink for trace gases, depending on their chemical property. The formation of surface water films and its influence on the gas deposition was proposed by many previous studies (Fuentes and Gillespie, 1992, Burkhardt and Eiden, 1994, van Hove et al., 1989, Burkhardt et al., 1999, Flechard et al., 1999). In this study we investigate the influence of leaf surface water films on the deposition of O3 and PAN under controlled laboratory conditions. A twin cuvette system described in Sun et al. (2015) was used to control the environmental parameters such as light, temperature, trace gas mixing ratio and humidity. Furthermore, the leaf surface was treated with various organic and inorganic solutions to investigate the influence of deposited compounds on the electrical surface conductance of the leaves and the surface deposition of O3 and PAN at various relative humidities. The result shows that RHcrit, where the electrical surface conductance (G) increases exponentially, was 40 % during the light period and 50 % during the dark period. Furthermore, we observed that the formation of the leaf surface liquid film was depended on the deposited compounds on the leaf cuticles. For the O3 deposition on plants (Quercus ilex) a clear enhancement at rising environmental air humidity under light and dark condition was found. The increase during light conditions can be related partly to increasing stomatal conductance with higher RH. From the non-stomatal deposition measured in dark experiments, we could

  3. Radionuclides, inorganic constituents, organic compounds, and bacteria in water from selected wells and springs from the southern boundary of the Idaho National Engineering Laboratory to the Hagerman Area, Idaho, 1991

    Energy Technology Data Exchange (ETDEWEB)

    Bartholomay, R.C.; Edwards, D.D. [Geological Survey, Idaho Falls, ID (United States); Campbell, L.J. [State of Idaho, Dept. of Water Resources (United States)

    1993-11-01

    The US Geological Survey and the Idaho Department of Water Resources, in response to a request from the US Department of Energy, sampled 18 sites as part of a long-term project to monitor water quality of the Snake River Plain aquifer from the southern boundary of the Idaho National Engineering Laboratory to the Hagerman area. Water samples were collected and analyzed for manmade pollutants and naturally occurring constituents. The samples were collected from six irrigation wells, seven domestic wells, two springs, one stock well, one dairy well, and one observation well. Quality assurance samples also were collected and analyzed. The water samples were analyzed for selected radionuclides, inorganic constituents, organic compounds, and bacteria. None of the samples analyzed for radionuclides, inorganic constituents, or organic compounds exceeded the established maximum contaminant levels for drinking water. Most of the radionuclide and inorganic constituent concentrations exceeded their respective reporting levels. All the samples analyzed for dissolved organic carbon had concentrations that exceeded their reporting level. Concentrations of 1,1,1 -trichloroethane exceeded the reporting level in two water samples. Two samples and a quality assurance replicate contained reportable concentrations of 2, 4-D. One sample contained fecal coliform bacteria counts that exceeded established maximum contaminant levels for drinking water.

  4. Radionuclides, stable isotopes, inorganic constituents, and organic compounds in water from selected wells and springs from the southern boundary of the Idaho National Engineering Laboratory to the Hagerman Area, Idaho, 1993

    Energy Technology Data Exchange (ETDEWEB)

    Bartholomay, R.C.; Edwards, D.D.; Campbell, L.J.

    1994-10-01

    The US Geological Survey and the Idaho Department of Water Resources, in response to a request from the US Department of Energy, sampled 19 sites as part of a long-term project to monitor water quality of the Snake River Plain aquifer from the southern boundary of the Idaho National Engineering Laboratory to the Hagerman area. Water samples were collected and analyzed for selected radionuclides, stable isotopes, inorganic constituents, and organic compounds. The samples were collected from seven irrigation wells, four domestic wells, two springs, one stock well, three dairy wells, one observation well, and one commercial well. Two quality assurance samples also were collected and analyzed. None of the radionuclide, inorganic constituent, or organic compound concentrations exceeded the established maximum contaminant levels for drinking water. Most of the radionuclide and inorganic constituent concentrations exceeded their respective reporting levels. All samples analyzed for surfactants and dissolved organic carbon had concentrations that equaled or exceeded their reporting levels. The ethylbenzene concentration in one water sample exceeded the reporting level.

  5. Evaluation of Toxicological Effects of an Aqueous Extract of Shells from the Pecan Nut Carya illinoinensis (Wangenh.) K. Koch and the Possible Association with Its Inorganic Constituents and Major Phenolic Compounds.

    Science.gov (United States)

    Porto, Luiz Carlos S; da Silva, Juliana; Sousa, Karen; Ambrozio, Mariana L; de Almeida, Aline; Dos Santos, Carla Eliete I; Dias, Johnny F; Allgayer, Mariangela C; Dos Santos, Marcela S; Pereira, Patrícia; Ferraz, Alexandre B F; Picada, Jaqueline N

    2016-01-01

    Background. Industrial processing of the pecan nut Carya illinoinensis K. Koch generated a large amount of shells, which have been used to prepare nutritional supplements and medicinal products; however, the safe use of shells requires assessment. This study evaluated the toxic, genotoxic, and mutagenic effects of pecan shell aqueous extract (PSAE) and the possible contribution of phenolic compounds, ellagic and gallic acids, and inorganic elements present in PSAE to induce toxicity. Results. Levels of inorganic elements like K, P, Cl, and Rb quantified using the Particle-Induced X-Ray Emission method were higher in PSAE than in pecan shells, while Mg and Mn levels were higher in shells. Mice showed neurobehavioral toxicity when given high PSAE doses (200-2,000 mg kg(-1)). The LD50 was 1,166.3 mg kg(-1). However, PSAE (50-200 mg·kg(-1)) and the phenolic compounds (10-100 mg·kg(-1)) did not induce DNA damage or mutagenicity evaluated using the comet assay and micronucleus test. Treatment with ellagic acid (10-100 mg·kg(-1)) decreased triglyceride and glucose levels, while treatments with PSAE and gallic acid had no effect. Conclusion. Pecan shell toxicity might be associated with high concentrations of inorganic elements such as Mn, Al, Cu, and Fe acting on the central nervous system, besides phytochemical components, suggesting that the definition of the safe dose should take into account the consumption of micronutrients.

  6. Synthesis, characterization and electrochemical investigation of a new inorganic-organic hybrid compound constructed by Keggin-type polyoxometalate and cyanoguanidine

    Science.gov (United States)

    Zonoz, Farrokhzad Mohammadi; Zonoz, Irandokht Mohammadi; Jamshidi, Ali; Alizadeh, Mohammad Hassan

    2014-06-01

    An inorganic-organic hybrid complex [HDCD]3[PW12O40]·3H2O (1) (DCD = 2-cyanoguanidine) has been synthesized from the reaction of Keggin polyanion and cyanoguanidine (C2N4H4) under mild condition, and characterized by using elemental analysis, infrared spectrum, thermogravimatric analysis and single crystal X-ray diffraction. X-ray crystallography reveals that 1 displays an inorganic-organic hybrid frameworks constructed by [PW12O40]3- Keggin-type polyoxoanion and three {(HDCD)}+ monocationic hydrogen-bonded units. The electrochemical behavior and electrocatalysis of 1 have been studied in detail.

  7. 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......, Hg, Tl, Pb, Bi. The subjects of compound identification and bringing insoluble compounds in solution by alcaline melt digestion are also treated. A high number of small experiments are described....

  8. Immobilization of L-Lysine on Zeolite 4A as an Organic-Inorganic Composite Basic Catalyst for Synthesis of α,β-Unsaturated Carbonyl Compounds under Mild Conditions

    Energy Technology Data Exchange (ETDEWEB)

    Zamani, Farzad; Rezapour, Mehdi; Kianpour, Sahar [Islamic Azad Univ., Isfahan (Iran, Islamic Republic of)

    2013-08-15

    Lysine (Lys) immobilized on zeolite 4A was prepared by a simple adsorption method. The physical and chemical properties of Lys/zeolite 4A were investigated by X-ray diffraction (XRD), FT-IR, Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and UV-vis. The obtained organic-inorganic composite was effectively employed as a heterogeneous basic catalyst for synthesis of α,β-unsaturated carbonyl compounds. No by-product formation, high yields, short reaction times, mild reaction conditions, operational simplicity with reusability of the catalyst are the salient features of the present catalyst.

  9. Investigations into effects on performance and glutathione peroxidase activity in broilers when increasing selenium contents of complete diets appropriate to animals' selenium requirements by adding different selenium compounds (organic vs. inorganic).

    Science.gov (United States)

    Salman, Mustafa; Muğlali, Omer Hakan; Selçuk, Zehra

    2009-06-01

    The aim of this study was to compare the effects of inorganic and organic selenium compounds supplementations to diets containing adequate selenium in broilers on performance, carcass traits, plasma and tissue glutathione peroxidase activity. A total of 150 one-day-old broilers were randomized into one control and two treatment groups each containing 50 birds; each group was then divided into 3 replicate groups. The experiment lasted 42 days. All groups were fed with broiler starter diet from day 1 to 21 and finisher diet from day 22 to 42. The basal diet for control group included adequate selenium due to vitamin-mineral premix and feeds. The basal diet was supplemented with 0.2 mg/kg organic selenium (selenomethionine, treatment group 1) and 0.2 mg/kg inorganic selenium (sodium selenite, treatment group 2). Although no significant differences were determined between treatment group 1 and the control group for mean body weights, the differences between the group given inorganic selenium and the other groups were statistically significant (p organic selenium to diets containing adequate selenium increased plasma, liver, femoral muscle, kidney and heart tissue glutathione peroxidase activity in broilers.

  10. Interaction of silicene and germanene with non-metallic substrates

    Science.gov (United States)

    Houssa, M.; Scalise, E.; van den Broek, B.; Lu, A.; Pourtois, G.; Afanas'ev, V. V.; Stesmans, A.

    2015-01-01

    By using first-principles simulations, we investigate the interaction of silicene and germanene with various non-metallic substrates. We first consider weak van der Waals interactions between the 2D layers and dichalcogenide substrates, like MoX2 (X=S, Se, Te). The buckling of the silicene or germanene layer is correlated to the lattice mismatch between the 2D material and the MoX2 template. The electronic properties of silicene or germanene on these different templates then largely depend on the buckling of the 2D material layer: highly buckled silicene or germanene on MoS2 are predicted to be metallic, while low buckled silicene on MoTe2 is predicted to be semi-metallic, with preserved Dirac cones at the K points. We next study the covalent bonding of silicene and germanene on (0001) ZnS and ZnSe surfaces. On these substrates, silicene or germanene are found to be semiconducting. Remarkably, the nature and magnitude of their energy band gap can be controlled by an out-of-plane electric field.

  11. The role of Jahn-Teller distortion in insulator to semiconductor phase transition in organic-inorganic hybrid compound (p-chloroanilinium)2CuCl4 at high pressure.

    Science.gov (United States)

    Ghalsasi, Pallavi; Garg, Nandini; Deo, M N; Garg, Alka; Mande, Hemant; Ghalsasi, Prasanna; Sharma, Surinder M

    2015-12-28

    (p-Chloroanilinium)2CuCl4(C2H14Cl6CuN2) is from an important family of organic-inorganic layered hybrid compounds which can be a possible candidate for multiferroicity. In situ high pressure FTIR, Raman and resistivity measurements on this compound indicate the weakening of Jahn-Teller distortion and the consequent removal of puckering of the CuCl6(4-) octahedra within the layer. These effects trigger insulator to semiconductor phase transition along with a change in the sample colour from yellow to dark red. This article explains the crucial role of the anisotropic volume reduction of the CuCl6(4-) octahedron (caused due to the quenching of Jahn-Teller distortion) in the observed insulator to semiconductor phase transition.

  12. Synthesis and Characterizaion of a New Inorganic-organic Sulfate Compound--Crystal Structure of [Ni(H2O)6][H2N(C2H4)2NH2](SO4)2

    Institute of Scientific and Technical Information of China (English)

    MENG He; XING Yan; FU Yun-long; SHI Zhan; PANG Wen-qin

    2004-01-01

    [Ni(H2O)6][H2N(C2H4)2NH2](SO4)2 is an inorganic-organic compound with a new open framework synthesized by hydrothermal method, and characterized by means of single-crystal diffraction and spectroscopic data. The compound crystallized in a monoclinic space group P21/n with a=1.29089(2) nm, b=1.06301(3) nm, c=1.33202(4) nm, β=114.0870(10)°, V=1.67127(8) nm3, Z=4, and was solved by using the direct method and the least-squares refinement converged at R=0.0214[I>2σ(I)]. The structure consists of isolated Ni(H2O)6 octahedra and SO4 tetrahedra, with both of them hydrogen-bonded to piperazine cations.

  13. Evaluation of Toxicological Effects of an Aqueous Extract of Shells from the Pecan Nut Carya illinoinensis (Wangenh. K. Koch and the Possible Association with Its Inorganic Constituents and Major Phenolic Compounds

    Directory of Open Access Journals (Sweden)

    Luiz Carlos S. Porto

    2016-01-01

    Full Text Available Background. Industrial processing of the pecan nut Carya illinoinensis K. Koch generated a large amount of shells, which have been used to prepare nutritional supplements and medicinal products; however, the safe use of shells requires assessment. This study evaluated the toxic, genotoxic, and mutagenic effects of pecan shell aqueous extract (PSAE and the possible contribution of phenolic compounds, ellagic and gallic acids, and inorganic elements present in PSAE to induce toxicity. Results. Levels of inorganic elements like K, P, Cl, and Rb quantified using the Particle-Induced X-Ray Emission method were higher in PSAE than in pecan shells, while Mg and Mn levels were higher in shells. Mice showed neurobehavioral toxicity when given high PSAE doses (200–2,000 mg kg−1. The LD50 was 1,166.3 mg kg−1. However, PSAE (50–200 mg·kg−1 and the phenolic compounds (10–100 mg·kg−1 did not induce DNA damage or mutagenicity evaluated using the comet assay and micronucleus test. Treatment with ellagic acid (10–100 mg·kg−1 decreased triglyceride and glucose levels, while treatments with PSAE and gallic acid had no effect. Conclusion. Pecan shell toxicity might be associated with high concentrations of inorganic elements such as Mn, Al, Cu, and Fe acting on the central nervous system, besides phytochemical components, suggesting that the definition of the safe dose should take into account the consumption of micronutrients.

  14. Three new three-dimensional organic-inorganic hybrid compounds based on PMo12O40(n-) (n = 3 or 4) polyanions and Cu(I)-pyrazine/Cu(I)-pyrazine-Cl porous coordination polymers.

    Science.gov (United States)

    Qi, Ming-Li; Yu, Kai; Su, Zhan-Hua; Wang, Chun-Xiao; Wang, Chun-Mei; Zhou, Bai-Bin; Zhu, Chun-Cheng

    2013-06-07

    Three new organic-inorganic hybrid compounds based on PMo12O40(n-) (n = 3 or 4) polyanions and Cu(I)-pz/Cu(I)-pz-Cl porous coordination polymers: [Cu(I)(pz)]3[PMo(VI)12O40] (1), [Cu(I)(pz)1.5]4[PMo(V)Mo(VI)11O40]·pz·2H2O (2), [Cu(I)3(pz)3Cl][Cu(I)2(pz)3(H2O)][PMo(V)Mo(VI)11O40] (3) (pz = pyrazine) have been hydrothermally prepared and characterized by elemental analysis, IR, TG, XRD, XPS and single-crystal X-ray diffraction. Compound 1 presents a three-dimensional Cu(I)-pz framework with cube-like chambers, into which PMo(VI)12O40(3-) Keggin ions are incorporated. Compound 2 shows a three-dimensional sandwich-like framework, and PMo(V)Mo(VI)11O40(4-) polyanions are located in the octagonal voids of every two-dimensional Cu(I)-pz 4(1)8(2) network structure. Compound 3 exhibits a two-dimensional Cl-bridged Cu(I)-pz-Cl double-layer structure, and two kinds of PMo(V)Mo(VI)11O40(4-) polyanions as bridging linkers connect two adjacent double-layers to form a three-dimensional organic-inorganic framework through Cu(I)-O bonds. Additionally, their electrochemical characters, electrocatalytic behaviors and solid state fluorescent properties at room temperature have been investigated in detail.

  15. 有机-无机复混肥对烤烟生长及产质量的影响%Effect of Organic-inorganic Compound Fertilizer on Growth,Yield and Quality of Flue-cured Tobacco

    Institute of Scientific and Technical Information of China (English)

    光映霞; 曹良波

    2011-01-01

    The effect of different types of organic-inorganic compound fertilizer on yield and quality of flue-cured tobacco was studied,in order to screen the best fertilizer varieties and the optimum amount of fertilization for tobacco production of Yunnan Zhaotong City.The results showed that: the application of organic-inorganic fertilizer could promote tobacco plant's growth and development,promote the leaves' growth,enter the vigorous growing period fast.The 'Zhenfa' organic-inorganic fertilizer was better in the field performance,yield increased by 0.79%~7.60%,output value increased by 4.48%~10.58% using the organic-inorganic compound fertilizer.Fertilier amount with 50% tobacco special fertilizer and 50% organic-inorganic fertilizer showed good performance in each index.The yield,output value,price and the proportion of high-quality leaves reached respectively 2 989.35 kg/hm2,40 007.85 yuan/hm2,13.39 yuan/kg,44.88% using 'Zhenfa' fertilizer.Application of organic-inorganic compound fertilizer could greatly improve the economic benefit of tobacco.%研究不同类型有机-无机复混肥对烤烟产质量的影响,筛选出适合云南昭通市烤烟生产上施用效果好的肥料品种及最佳施肥量,试验结果表明:施用有机-无机复混肥能促进烟株早生快发,叶片开片好,进入旺长期快,以"珍发"牌有机-无机复混肥田间表现较好,施用有机-无机复混肥烟叶产量提高0.79%~7.60%,产值提高4.48%~10.58%。以50%烟草专用肥+50%有机-无机复混肥施肥处理的各项指标较好,其中以50%烟草专用肥+50%"珍发"牌有机-无机复混肥处理最佳,产量、产值、均价及上等烟比例分别为2 989.35 kg/hm2、40 007.85元/hm2、13.39元/kg、44.88%。施用有机-无机复混肥能大幅提高烟叶的经济效益。

  16. A RISK MANAGEMENT METHODOLOGY FOR NON-METALLIC PROCESS EQUIPMENT

    Directory of Open Access Journals (Sweden)

    J.J. Viviers

    2012-01-01

    Full Text Available

    ENGLISH ABSTRACT: Many companies in South Africa have implemented the risk-based inspection (RBI methodology as a maintenance strategy. The risk involved in operating a piece of equipment, past history, non-destructive examination techniques, failure modes, and many other aspects determine the frequency of inspections required to meet legislation. The main purpose of the RBI methodology is to prevent failures of process equipment. The methodology for risk-based inspection for metal equipment is well-established and has been proven in industry, becoming the norm nationally and internationally. However, it is not possible to apply all the techniques to nonmetallic equipment owing to vast differences between the two types of materials. This paper discusses the results of data gathered on the RBI methodology for nonmetallic equipment, and proposes a risk-based model that can be used to perform a risk assessment for non-metallic equipment in a process plant. The risk assessment can be used to formulate the next inspection interval for the asset.

    AFRIKAANSE OPSOMMING: Verskeie maatskappye in Suid-Afrika het reeds die metodologie van risikogebaseeerde inspeksie (RBI geïmplementeer as deel van ‘n omvattende instandhoudingstrategie. Die risiko betrokke by ‘n fisiese item, bedryfsgeskiedenis, nie-vernietigende toetstegnieke, falingsmodusse, en vele ander aspekte bepaal die frekwensie van inspeksies wat benodig word om aan wetlike vereistes te voldoen. Die hoofdoel van die risiko-gebaseerde metodologie is om faling van prosestoerusting te verhinder. Die metodologie vir risiko-gebaseerde inspeksie van metaaltoerusting is goed bekend en word suksesvol toegepas in die industrie. Dis is egter nie moontlik om al die tegnieke toe te pas op nie-metaaltoerusting nie weens die groot verskeidenheid van materiaaltipes. Hierdie artikel bespreek die data wat ingewin is op die risiko-gebaseerde metodologie vir nie-metaaltipeprosestoerusting, en stel

  17. New Inorganic-organic Hybrid Compound Containing One Dimensional Keggin Polyoxometalate[SiW11O39Co]6- Chains:Preparation,Characterization and Application in Chemically Bulk-modified Electrode

    Institute of Scientific and Technical Information of China (English)

    WANG Xiu-li; LIN Hong-yan; LIU Guo-cheng; CHEN Bao-kuan; BI Yan-feng

    2008-01-01

    A new inorganic-organic hybrid compound based on polyoxometalate and organic ligand formulated as (H2bpp)3[SiW11O39Co]~2H2O(1)[bpp=1,3-bis(4-pyridyl)propane]was hydrothermally synthesized and structurally characterized by elemental analysis,single-crystal X-ray diffraction,IR,TG,and cyclic voltammetry.Single-crystal X-ray diffraction analysis reveals that compound 1 consists of interesting cobalt-monosubstituted POMs one dimensional chain together with protonated bpp ligands.Additionally,the polyoxoanions combined with the discrete organic substrates by hydrogen bond interactions to afford a supramolecular 3D network structure.The hybrid compound 1 was used as a bulk modifier to fabricate a three-dimensional chemically modified carbon paste electrode(1-CPE)by direct mixing.The electrochemical behavior and electrocatalysis of 1-CPE were studied in detail.The results indicate that 1-CPE has good electrocatalytic activities toward the reduction of nitrite or bromate in 1mol/L H2SO4 aqueous solution.1-CPE shows remarkable stability that can be ascribed to the insolubility of compound 1 and the supramolecular interactions existed between 1D POM anion chains and organic ligand bpp,which is very important for practical applications in electrode modification.

  18. A theoretical study on the molecular structure and vibrational (FT-IR and Raman) spectra of new organic-inorganic compound [N(C3H7)4]2SnCl6.

    Science.gov (United States)

    Hajlaoui, Sondes; Chaabane, Iskandar; Oueslati, Abderrazak; Guidara, Kamel; Bulou, Alain

    2014-01-03

    Tetrapropylammoniumchloride was used as a ligand for the synthesis of the new organic-inorganic compound bis-tetrapropylammoniumhexachlorostannate. Vibrational study in the solid state was performed by FT-IR of the free Tetrapropylammoniumchloride ligand (TPACL) and by FT-IR and FT-Raman spectroscopies of the [N(C3H7)4]2SnCl6 compound. The comparative analysis of the Infrared spectra of the title compound with that of the free ligand was discussed. The structure of the [N(C3H7)4]2SnCl6 compound was optimized by density functional theory (DFT) using B3LYP method and shows that the calculated values obtained by B3LYP/LanL2MB basis are in much better agreement with the experimental data than those obtained by B3LYP/LanL2DZ. The vibrational frequencies were evaluated using density functional theory (DFT) with the standard B3LYP/LanL2MB basis, and were scaled using various scale factors. Root mean square (RMS) value was calculated and the small difference between experimental and calculated modes has been interpreted by intermolecular interactions in the crystal. Copyright © 2013 Elsevier B.V. All rights reserved.

  19. A new paratungstate-A-based organic-inorganic hybrid compound: Synthesis, structure and photocatalytic property of [Co(en)3]2[H2W7O24]·8H2O

    Science.gov (United States)

    Yan, Gang; Wang, Xin; Ma, Yuanyuan; Cheng, Xin; Wang, Yonghui; Li, Yangguang

    2013-03-01

    A new paratungstate-A-based organic-inorganic hybrid compound with the chemical formula of [Co(en)3]2[H2W7O24]·8H2O (en = ethylenediamine) (1) has been hydrothermally synthesized and structurally characterized by the elemental analysis, IR, TG, powder X-ray diffraction (PXRD) and single-crystal X-ray diffraction. Compound 1 crystallizes in the monoclinic space group P21/c with a = 17.216(3) Å, b = 14.986(3) Å, c = 23.088(8) Å, β = 128.151(2)°, V = 4684.2 Å3, Z = 1, R1 = 0.0484, and wR2 = 0.1087. The structure of 1 consists of the [H2W7O24]4- building blocks and [Co(en)3]2+ metal-organic cationic moieties, which are packed together via the electrostatic forces and extensive hydrogen-bonding interactions to form a three-dimensional supramolecular framework. Interestingly, compound 1 represents the first structurally-defined hybrid compound based on the metastable paratungstate-A polyoxoanions and metal-organic units. The degradation of Rhodamine-B (RhB) under UV irradiation with 1 as the heterogeneous photocatalyst has been investigated, showing a good photocatalytic property of 1 for RhB degradation.

  20. 油桐饼粕有机-无机复混肥的生产工艺%Study on the Producing Technology of Organic-inorganic Compound Fertilizer Using Tung Oil Cake

    Institute of Scientific and Technical Information of China (English)

    郑威; 刘金龙; 罗兴武; 佃国党

    2011-01-01

    Organic-inorganic compound fertilizer was produced from tung oil cake. The granulation parameters were optimized by orthogonal test based on single factor experiments. And the nutrition compounds in the fertilizer and raw material were tested. The results showed that when the fertilizer formula was tobacco stem 64%+tung oil cake 11%+ NH4H2PO4 25%, the optimum granulation parameters were, fineness of raw material 300 holes, dosage of adhesive 20 g/kg, dosage of water 300 g/kg. The content of N, P, K in organic-inorganic compound fertilizer reached 16.90%. This product had high effectiveness, could improve soil quality and control pests to some extent.%设计产品配方生产油桐饼粕有机-无机复混肥,在单因素试验的基础上进行正交试验,得出最佳造粒参数,并对原料和产品的营养成分进行检测.结果表明,按发酵烟茎、发酵油桐饼柏、磷酸一铵质量比为64∶11∶25的配方生产油桐饼粕有机-无机复混肥,最佳造粒参数为原料粉碎成粒度为300目的粉末,黏合剂用量20 g/kg,加水量300 g/kg,生产的油桐饼粕有机-无机复混肥中氮、磷、钾总含量达16.90%.该产品肥效高,可改良土壤,还能够防治农田害虫,是有机-无机复混肥中的新品种.

  1. Crystal structure, thermal studies, Hirshfeld surface analysis, vibrational and DFT investigation of organic-inorganic hybrid compound [C9H6NOBr2]2CuBr4·2H2O

    Science.gov (United States)

    Mesbeh, Radhia; Hamdi, Besma; Zouari, Ridha

    2016-12-01

    Single crystals of a hybrid organic/inorganic material with the formula [C9H6NOBr2]2CuBr4·2H2O were studied by X-ray diffraction. The compound crystallizes in the monoclinic system, space group C2/c with the following unit cell parameters: a = 7.8201 (12) Ǻ, b = 18.203 (3) Ǻ, c = 19.486 (3) Ǻ, β = 98.330 (5)°, Z = 4, V = 2744.6 (7) Ǻ3. Crystal structure was solved with a final R = 5.66% for 3483 independent reflections. The atomic arrangement shows an alternation of organic and inorganic layers. Between layers, the cohesion is performed via Osbnd H⋯Br, Csbnd H⋯Br, Nsbnd H⋯Br, Nsbnd H⋯O and Osbnd H⋯O hydrogen bending. Thermogravimetric analysis (TGA) and differential thermal analysis (DTA) measurements have been carried out on [C9H6NOBr2]2CuBr4·2H2O crystal in the temperature range between 50 and 500 °C. The assignment of the observed bands in the solid state FTIR and Raman spectra of the compound was assisted by the theoretically predicted frequencies and compared with data previously reported for similar compounds. The theoretical geometrical parameters in the ground state have been investigated by density functional theory (DFT) with the B3LYP/LanL2DZ level of theory. The optical properties were investigated by optical absorption and show two bands at 279, 300 nm. The percentages of hydrogen bonding interactions are analyzed by Fingerprint plots of Hirshfeld surface.

  2. Absorption of non-metallic inclusions by steelmaking slags—a review

    Directory of Open Access Journals (Sweden)

    Bruno Henrique Reis

    2014-04-01

    Full Text Available The formation of non-metallic inclusions during steelmaking is inevitable and, when not properly controlled, can cause performance and production problems. Slag is one of the resources available to carry out this control. In steelmaking, it is generally understood that inclusions are naturally absorbed by slag when flotation is sufficient. However, separation and dissolution may define the inclusion absorption capacity of slag. The discussion in this review explains the relationship between separation and the contact angle at the steel/inclusion interface, which differentiates the mechanism from liquid and solid inclusions. Whereas liquid particles show more predictable behavior in experimental observations, thermodynamic analysis is necessary in order to describe the removal of solid particles. Among other findings, it is evident that slag viscosity and the formation of compounds at the inclusion/slag interface strongly influence inclusion dissolution capacity. Following a detailed description of findings in the literature, this review considers the most influential factors to aid in optimizing slags for inclusion absorption.

  3. Comparison of abundances, compositions and sources of elements, inorganic ions and organic compounds in atmospheric aerosols from Xi'an and New Delhi, two megacities in China and India.

    Science.gov (United States)

    Li, Jianjun; Wang, Gehui; Aggarwal, Shankar G; Huang, Yao; Ren, Yanqin; Zhou, Bianhong; Singh, Khem; Gupta, Prabhat K; Cao, Junji; Zhang, Rong

    2014-04-01

    Wintertime TSP samples collected in the two megacities of Xi'an, China and New Delhi, India were analyzed for elements, inorganic ions, carbonaceous species and organic compounds to investigate the differences in chemical compositions and sources of organic aerosols. The current work is the first time comparing the composition of urban organic aerosols from China and India and discussing their sources in a single study. Our results showed that the concentrations of Ca, Fe, Ti, inorganic ions, EC, PAHs and hopanes in Xi'an are 1.3-2.9 times of those in New Delhi, which is ascribed to the higher emissions of dust and coal burning in Xi'an. In contrast, Cl(-), levoglucosan, n-alkanes, fatty alcohols, fatty acids, phthalates and bisphenol A are 0.4-3.0 times higher in New Delhi than in Xi'an, which is attributed to strong emissions from biomass burning and solid waste incineration. PAHs are carcinogenic while phthalates and bisphenol A are endocrine disrupting. Thus, the significant difference in chemical compositions of the above TSP samples may suggest that residents in Xi'an and New Delhi are exposed to environmental hazards that pose different health risks. Lower mass ratios of octadecenoic acid/octadecanoic acid (C18:1/C18:0) and benzo(a)pyrene/benzo(e)pyrene (BaP/BeP) demonstrate that aerosol particles in New Delhi are photochemically more aged. Mass closure reconstructions of the wintertime TSP indicate that crustal material is the most abundant component of ambient particles in Xi'an and New Delhi, accounting for 52% and 48% of the particle masses, respectively, followed by organic matter (24% and 23% in Xi'an and New Delhi, respectively) and secondary inorganic ions (sulfate, nitrate plus ammonium, 16% and 12% in Xi'an and New Delhi, respectively). Copyright © 2014 Elsevier B.V. All rights reserved.

  4. Estimating intestinal absorption of inorganic and organic selenium compounds by in vitro flux and biotransformation studies in Caco-2 cells and ICP-MS detection

    DEFF Research Database (Denmark)

    Gammelgaard, Bente; Rasmussen, Laura Hyrup; Gabel-Jensen, Charlotte

    2012-01-01

    selenite and MeSeA fluxes correlated to poor in vivo absorption. Speciation analysis of cell lysate and donor and receptor solutions by LC-ICP-MS showed limited transformation of all selenium compounds. Extensive transformation as well as significantly increased absorptive flux was observed when co......SeA, including volatile species, whereas no significant increases in fluxes were observed. In summary, the absorption of selenite selenate and the selenoamino acids is considered complete under physiological conditions, but the absorption mechanisms and metabolism of the compounds are different. © 2011 Springer......The aim of the present work was to compare and estimate absorption and biotransformation of selected selenium compounds by studying their fluxes across Caco-2 cells. Five different selenium compounds, selenomethionine (SeMet), Se-methylselenocysteine (MeSeCys), selenate, selenite...

  5. Production of organic-inorganic compound fertilizer by extruding granulation polishing circle process%挤压造粒抛圆工艺生产有机-无机复混肥

    Institute of Scientific and Technical Information of China (English)

    周洪亮

    2012-01-01

    介绍挤压造粒抛圆工艺生产有机肥和有机-无机复混肥的工艺流程和工艺创新点。采用有机废弃物经好氧发酵得到的有机肥原料颗粒大,堆积密度小,宜采用三级组合抛光挤压造粒设备生产,生产的有机-无机复混肥成球率高达90%以上,强度大,成球水分低(w(H2O)不超过20%),且吨肥能耗低。%The extruding granulation polishing circle process for production of organic fertilizer and organic-inorganic compound fertilizer and its innovations are introduced. The organic fertilizer raw material is obtained from organic waste by aerobic fermentation, the particle is big, the stacking density is small, through using three-level combination polishing extruding granulation equipment, the ball rate of organic-inorganic fertilizer is above 90%, the particle strength is high, the w(H2O) is less than 20%, and the energy consumption per ton product is low.

  6. Sodium dimercaptopropane sulfonate as antidote against non-metallic pesticides

    Institute of Scientific and Technical Information of China (English)

    Zhi-kang CHEN; Zhong-qiu LU

    2004-01-01

    @@ INTRODUCTION With the advent of World War II, dimercaptol was first developed in England as an effective antidote against arsenical agents. In 1950' s, scientists from the Soviet Union developed a water-soluble compound, sodium dimercaptopropane sulfonate (Na-DMPS) named as Unithiol (or Unitiol), which was able to chelate heavy metals and metalloids.

  7. Sequential extraction of inorganic arsenic compounds and methyl arsenate in human urine using mixed-mode monolithic silica spin column coupled with gas chromatography-mass spectrometry.

    Science.gov (United States)

    Namera, Akira; Takeuchi, Akito; Saito, Takeshi; Miyazaki, Shota; Oikawa, Hiroshi; Saruwatari, Tatsuro; Nagao, Masataka

    2012-09-01

    A sequential analytical method was developed for the detection of arsenite, arsenate, and methylarsenate in human urine by gas chromatography-mass spectrometry (GC-MS). The combination of a derivatization of trivalent arsenic compounds by 2,3-dithio-1-propanol (British antilewisite; BAL) and a reduction of pentavalent arsenic compounds (arsenate and methylarsenate) were accomplished to carry out the analysis of arsenic compounds in urine. The arsenic derivatives obtained using BAL were extracted in a stepwise manner using a monolithic spin column and analyzed by GC-MS. A linear curve was observed for concentrations of arsenic compounds of 2.0 to 200 ng/mL, where the correlation coefficients of calibration curves were greater than 0.996 (for a signal-to-noise (S/N) ratio >10). The detection limits were 1 ng/mL (S/N > 3). Recoveries of the targets in urine were in the range 91.9-106.5%, and RSDs of the intra- and interday assay for urine samples containing 5, 50, and 150 ng/mL of arsenic compounds varied between 2.95 and 13.4%. The results from real samples obtained from a patient suspected of having ingested As containing medications using this proposed method were in good agreement with those obtained using high-performance liquid chromatography with inductively coupled plasma mass spectrometry.

  8. Size of Non-Metallic Inclusions in High-Grade Medium Carbon Steel

    OpenAIRE

    Lipiński T.; Wach A.

    2014-01-01

    Non-metallic inclusions found in steel can affect its performance characteristics. Their impact depends not only on their quality, but also, among others, on their size and distribution in the steel volume. The literature mainly describes the results of tests on hard steels, particularly bearing steels. The amount of non-metallic inclusions found in steel with a medium carbon content melted under industrial conditions is rarely presented in the literature. The tested steel was melted in an el...

  9. The Effect of Different Non-Metallic Inclusions on the Machinability of Steel

    OpenAIRE

    Niclas Ånmark; Andrey Karasev; Pär Göran Jönsson

    2015-01-01

    Considerable research has been conducted over recent decades on the role of non-metallic inclusions and their link to the machinability of different steels. The present work reviews the mechanisms of steel fractures during different mechanical machining operations and the behavior of various non-metallic inclusions in a cutting zone. More specifically, the effects of composition, size, number and morphology of inclusions on machinability factors (such as cutting tool wear, power consumption, ...

  10. Thermodynamics of Organic Compounds

    Science.gov (United States)

    1979-01-01

    General Techniques for Combustion of Liquid/Soli. Organic Compounds by Oxygen Bomb Calorimetry by Arthur J. Head, William D. Good, and Ccrnelius...Mosselman, Chap. 8; Combustion of Liquid/Solid Organic Compounds with Non-Metallic Hetero-Atoms by Arthur J. Head and William D. Good, Chap. 9; in...0 Box 95085 Washington, DC 20234 Los Angeles, CA 90045 National Bureau of Standards CINDAS Chemical Thermodynamics Division Purdue University

  11. Modification of Non-Metallic Inclusions by Rare-Earth Elements in Microalloyed Steels

    Directory of Open Access Journals (Sweden)

    M. Opiela

    2012-04-01

    Full Text Available The modification of the chemical composition of non-metallic inclusions by rare-earth elements in the new-developed microalloyed steels was discussed in the paper. The investigated steels are assigned to production of forged elements by thermo- mechanical treatment. The steels were melted in a vaccum induction furnace and modification of non-metallic inclusions was carried out by the michmetal in the amount of 2.0 g per 1 kg of steel. It was found that using material charge of high purity and a realization of metallurgical process in vacuous conditions result in a low concentration of sulfur (0.004%, phosphorus (from 0.006 to 0.008% and oxygen (6 ppm. The high metallurgical purity is confirmed by a small fraction of non-metallic inclusions averaging 0.075%. A large majority of non-metallic inclusions are fine, globular oxide-sulfide or sulfide particles with a mean size 17m2. The chemical composition and morphology of non-metallic inclusions was modified by Ce, La and Nd, what results a small deformability of non- metallic inclusions during hot-working.

  12. 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)

  13. Syntheses, structures and photocatalytic properties of five new praseodymium-antimony oxochlorides: from discrete clusters to 3D inorganic-organic hybrid racemic compounds.

    Science.gov (United States)

    Zou, Guo-Dong; Wang, Ze-Ping; Song, Ying; Hu, Bing; Huang, Xiao-Ying

    2014-07-14

    Five novel praseodymium-antimony oxochloride (Pr-Sb-O-Cl) cluster-based compounds, namely (2-MepyH)2[Fe(1,10-phen)3]2[Pr4Sb12O18Cl14.6(OH)2.4(Hsal)]·H2O (1), (2-MepyH)2[Fe(1,10-phen)3]4{[Pr4Sb12O18Cl13.5(OH)0.5](bcpb)2[Pr4Sb12O18Cl13.5(OH)0.5]}·42H2O (2), (3-MepyH)2[Fe(1,10-phen)3]{[Pr4Sb12O18Cl13(H2O)2](bcpb)}·2(3-Mepy)·3H2O (3), [Fe(1,10-phen)3]2{[Pr4Sb12O18Cl10(H2O)2](bcpb)2}·3(3-Mepy)·13H2O (4), and (2-MepyH)6[Fe(1,10-phen)3]10{[Pr4Sb12O18Cl13(OH)2]2[Pr4Sb12O18Cl9][Pr4Sb12O18Cl9(OH)2]2(Hpdc)10(pdc)2}·110H2O (5) (2-Mepy = 2-methylpyridine, 3-Mepy = 3-methylpyridine, 1,10-phen = 1,10-phenanthroline, H2sal = salicylic acid, H3bcpb = 3,5-bis(4-carboxyphenoxy)benzoic acid, H3pdc = 3,5-pyrazoledicarboxylic acid) have been solvothermally synthesized and structurally characterized. Compound 1 is the first zero-dimensional (0D) Pr-Sb-O-Cl cluster decorated by an organic ligand. Compounds 2-4 are constructed from the same H3bcpb ligands but adopt different structures: 2 represents a rare example of a one-dimensional (1D) nanotubular structure based on high-nuclearity clusters; 3 exhibits a two-dimensional (2D) mono-layered structure, in which left-handed and right-handed helical chains are alternately arranged, while 4 features a double-layered structure with an unprecedented (3,3,6)-connected 3-nodal topological net. Compound 5 is a unique three-dimensional (3D) 2-fold interpenetrating racemic compound, simultaneously containing three kinds of Pr-Sb-O-Cl-pdc clusters. UV-light photocatalytic H2 evolution activity was observed for compound 3 with Pt as a co-catalyst and MeOH as a sacrificial electron donor. In addition, the magnetic properties of compounds 1 and 5 are also studied.

  14. Determination of inorganic compounds in drinking water on the basis of house water heater scale, part 1: Determination of heavy metals and uranium

    Directory of Open Access Journals (Sweden)

    Rajković Miloš B.

    2004-01-01

    Full Text Available The analysis of scale originated from drinking water on the house water heater, showed that scale is basically calcium carbonate that crystallizes hexagonally in the form of calcite. Scale taken as a sample from different spots in Belgrade – upper town of Zemun (sample 1 and Pančevo (sample 2 showed different configuration although it came from the same waterworks. That indicates either that the water flowing through waterworks pipes in different parts of the city is not the same or the waterworks net is not the same (age, maintaining, etc. All the elements which are dominant in drinking water (Ca, Mg, K, and Na, and which could be found in water by natural processes, are by their content far below the values regulated by law. The analysis also showed the presence of many metals: Ti, Pb, Zn, Cu Li, Sr, Cd, and Cr in the first sample, which are not found in the scale taken near Pančevo. The results obtained by calculating the mass concentration in drinking water on the basis of scale content, showed that both waters belonged to the category of low mineral waters. Contents of inorganic substances in these waters (117.85 mg/dm3 for sample 1 or 80.83 mg/dm3 for sample 2 are twice lower than the values predicted by the legislation. Gammaspectrometric analysis indicates the presence of radioactive elements – uranium and strontium which can influence human health.

  15. 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. [...

  16. Responses of rice-wheat rotation system in south Jiangsu to organic-inorganic compound fertilizers%苏南地区稻麦轮作系统对不同有机无机复混肥的响应

    Institute of Scientific and Technical Information of China (English)

    田亨达; 张丽; 张坚超; 王秋君; 徐大兵; 哈丽哈什·依巴提; 徐佳乐; 黄启为

    2011-01-01

    In 2006-2007, a field trial was conducted to study the effects of applying three kinds of organic-inorganic compound fertilizers [ rapeseed cake compost plus inorganic fertilizers ( RCC ) , pig manure compost plus inorganic fertilizers ( PMC ) , and Chinese medicine residues plus inorganic fertilizers (CMC) ] on the crop growth and nitrogen (N) use efficiency of rice-wheat rotation system in South Jiangsu. Grain yield of wheat and rice in the different fertilization treatments was significantly higher than the control (no fertilization). In treatments RCC, PMC and CMC, the wheat yield was 13.1% , 32.2% and 39.3% lower than that of the NPK compound fertilizer (CF, 6760 kg · Hm-2), respectively, but the rice yield (8504-9449 kg · Hm-2) was significantly higher than that (7919 kg · Hm-2 ) of CF, with an increment of 7.4%-19.3%. In wheat season, the aboveground dry mass, N accumulation, and N use efficiency in treatments RCC, PMC, and CMC were lower than those of CF, but in rice season, these parameters were significantly higher than or as the same as CF. In sum, all the test three compound fertilizers had positive effects on the rice yield and its nitrogen use efficiency in the rice-wheat rotation system, being most significant for RCC.%通过田间试验,研究了苏南地区2006-2007年稻麦轮作体系下,施用菜粕堆肥有机无机复混肥(RCC)、猪粪堆肥有机无机复混肥(PMC)、中药渣堆肥有机无机复混肥(CMC)和化肥(CF)对小麦和水稻;产量及氮素利用率的影响.结果表明:各施肥处理的小麦和水稻产量均显著高于对照;RCC、PMC和CMC处理的小麦产量分别比化肥处理(6760 kg·hm-2)减少了13.1%、32.2%和39.3%;而不同有机无机复混肥处理的水稻产量(8504~9449 kg·hm-2)则显著高于化肥处理(7919 kg·hm-2),增产率达7.4%~19.3%.在小麦季,RCC、PMC和CMC处理的地上部干物质量、氮素积累量、氮素利用率普遍低于化肥处理,而水稻季则显

  17. Synthesis of Dichlorophosphinenickel(II) Compounds and Their Catalytic Activity in Suzuki Cross-Coupling Reactions: A Simple Air-Free Experiment for Inorganic Chemistry Laboratory

    Science.gov (United States)

    Thananatthanachon, Todsapon; Lecklider, Michelle R.

    2017-01-01

    In this experiment, students perform an air-free synthesis of three dichlorophosphinenickel(II) compounds, NiCl[subscript 2](PPh[subscript 3])[subscript 2], NiCl[subscript 2](PCy[subscript 3])[subscript 2], and NiCl[subscript 2](DPPE), using NiCl[subscript 2]·6H[subscript 2]O and the appropriate phosphine as the precursors. These colorful nickel…

  18. Estimating intestinal absorption of inorganic and organic selenium compounds by in vitro flux and biotransformation studies in Caco-2 cells and ICP-MS detection.

    Science.gov (United States)

    Gammelgaard, Bente; Rasmussen, Laura Hyrup; Gabel-Jensen, Charlotte; Steffansen, Bente

    2012-02-01

    The aim of the present work was to compare and estimate absorption and biotransformation of selected selenium compounds by studying their fluxes across Caco-2 cells. Five different selenium compounds, selenomethionine (SeMet), Se-methylselenocysteine (MeSeCys), selenate, selenite, and methylseleninic acid (MeSeA), were applied to Caco-2 cells in a concentration of 10 μM, and fluxes in both directions were studied for 2 h. Fluxes of selenite and MeSeA in the presence of excess reduced glutathione (selenite + GSH and MeSeA + GSH) and flux of MeSeA in the presence of excess cysteine (MeSeA + Cys) were also studied. Selenium absorptive and exsorptive fluxes and accumulation in cell cytosol were analyzed by means of flow injection inductively coupled plasma mass spectrometry (ICP-MS). Absorptive flux of SeMet, MeSeCys, and selenate showed values correlating to complete in vivo absorption, while selenite and MeSeA fluxes correlated to poor in vivo absorption. Speciation analysis of cell lysate and donor and receptor solutions by LC-ICP-MS showed limited transformation of all selenium compounds. Extensive transformation as well as significantly increased absorptive flux was observed when co-administering selenite with glutathione compared to administering selenite alone. These observations are possibly due to formation of selenodiglutathione (GS-Se-SG) which may be absorbed differently than selenite. Concomitant application of GSH or cysteine with MeSeA resulted in extensive transformation of MeSeA, including volatile species, whereas no significant increases in fluxes were observed. In summary, the absorption of selenite selenate and the selenoamino acids is considered complete under physiological conditions, but the absorption mechanisms and metabolism of the compounds are different.

  19. Polybenzimidazole compounds

    Science.gov (United States)

    Klaehn, John R.; Peterson, Eric S.; Wertsching, Alan K.; Orme, Christopher J.; Luther, Thomas A.; Jones, Michael G.

    2010-08-10

    A PBI compound that includes imidazole nitrogens, at least a portion of which are substituted with an organic-inorganic hybrid moiety. At least 85% of the imidazole nitrogens may be substituted. The organic-inorganic hybrid moiety may be an organosilane moiety, for example, (R)Me.sub.2SiCH.sub.2--, where R is selected from among methyl, phenyl, vinyl, and allyl. The PBI compound may exhibit similar thermal properties in comparison to the unsubstituted PBI. The PBI compound may exhibit a solubility in an organic solvent greater than the solubility of the unsubstituted PBI. The PBI compound may be included in separatory media. A substituted PBI synthesis method may include providing a parent PBI in a less than 5 wt % solvent solution. Substituting may occur at about room temperature and/or at about atmospheric pressure. Substituting may use at least five equivalents in relation to the imidazole nitrogens to be substituted or, preferably, about fifteen equivalents.

  20. 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.

  1. Two novel POM-based inorganic-organic hybrid compounds: synthesis, structures, magnetic properties, photodegradation and selective absorption of organic dyes.

    Science.gov (United States)

    Dui, Xue-Jing; Yang, Wen-Bin; Wu, Xiao-Yuan; Kuang, Xiaofei; Liao, Jian-Zhen; Yu, Rongmin; Lu, Can-Zhong

    2015-05-28

    The hydrothermal reactions of a mixture of (NH4)6Mo7O24·4H2O, Cu(Ac)2·H2O and 3-bpo ligands at different temperatures result in the isolation of two novel inorganic-organic hybrid materials containing different but related isopolymolybdate units, [Cu(3-bpo)(H2O)(Mo4O13)]·3H2O () and [Cu2(3-bpo)2(Mo6O20)] (). The {Mo4O13}n chains in and unprecedented [Mo6O20](4-) isopolyhexamolybdate anions in are linked by octahedral Cu(2+) ions into two-dimensional hybrid layers. Interestingly, 3-bpo ligands in both and are located on either side of these hybrid layers and serve as arched footbridges to link Cu(ii) ions in the layer via pyridyl N-donors, and at the same time connect these hybrid layers into 3D supramolecular frameworks via weak MoNoxadiazole bonds. Another important point for is that water clusters are filled in the 1D channels surrounded by isopolytetramolybdate units. In addition, dye adsorption and photocatalytic properties of and magnetic properties of have been investigated. The results indicated that complex is not only a good heterogeneous photocatalyst in the degradation of methyl orange (MO) and methylene blue (MB), but also has high absorption capacity of MB at room temperature and can selectively capture MB molecules from binary mixtures of MB/MO or MB/RhB. All MB molecules absorbed on can be completely released and photodegraded in the presence of adequate peroxide. The temperature dependence of magnetic susceptibility revealed that complex exhibits antiferromagnetic ordering at about 5 K, and a spin-flop transition was observed at about 5.8 T at 2 K, indicating metamagnetic-like behaviour from antiferromagnetic to ferromagnetic phases.

  2. First-principles Study on the Magnetic, Half-metal and Thermoelectric Transport Properties of Inorganic-Organic Hybrid Compounds [C4N2H12] [Fe4Ⅱ(HPO3)2(C2O4)3

    Institute of Scientific and Technical Information of China (English)

    LI Yan-Li; ZHANG Dian-Na

    2013-01-01

    The electronic structure,magnetic and half-metal properties of inorganic-organic hybrid compound [C4N2H12] [F4Ⅱ(HPO3)2(C2O4)3] are investigated by using the full-potential linearized augmented plane wave (FPLAPW)method within density-functional theory (DFT) calculations.The density of states (DOS),the total energy of the cell and the spontaneous magnetic moment of [C4N2H12] [Fe4Ⅱ(HPO3)2(C2O4)3] are calculated.The calculation results reveal that the low-temperature phase of [C4N2H12][Fe4Ⅱ (HPO3)2 (C2O4)3] exhibits a stable ferromagnetic (FM) ground state,and we find that this organic compound is a half-metal in FM state.In addition,we have calculated antiferromagnetically coupled interactions,revealing the existence of antiferromagnetic (AFM),which is in agreement with the experiment.We have also found that [C4N2H12][Fe4Ⅱ (HPO3)2(C2O4)3] is a semiconductor in the AFM state with a band gap of about 0.40 eV.Subsequently,the transport properties for potential thermoelectric applications have been studied in detail based on the Boltzmann transport theory.

  3. Synthesis, property and crystal structure of a novel two-dimensional network organic-inorganic hybrid compound based on the neodymium III center and Keggin-type heteropolyanion of [α-BW 12O 40] 5-

    Science.gov (United States)

    Niu, Jingyang; Zhao, Junwei; Wang, Jingping; Ma, Pengtao

    2004-08-01

    A novel two-dimensional infinite network organic-inorganic hybrid neodymium(III)-centered compound of formula (dmaH) 2[Nd(dmf) 4(H 2O)][α-BW 12O 40]·H 2O ( 1) [dma=dimethylamine and dmf= N, N-dimethylformamide] is obtained by the conventional self-assembly reaction of neodymium oxide, N, N-dimethylformamide and borotungstic acid (α-H 5BW 12O 40·30H 2O) in the mixed solvent of acetonitrile and water, and characterized by IR, UV-visible spectra and X-ray single crystal diffraction. Structural analysis indicates that every [α-BW 12O 40] 5- polyanion interconnects with three adjacent [Nd(dmf) 4(H 2O)] 3+ subunits by means of W-O-Nd bridges, meanwhile, every [Nd(dmf) 4(H 2O)] 3+ building block is surrounded by three neighboring [α-BW 12O 40] 5- polyanions by making use of which an unprecedented two-dimensional extended network structure can be constructed. Interestingly, this structure pattern may act as useful model for the design and assembly of functional molecule-based compounds, especially in the field of molecular sieve materials.

  4. DFT (B3LYP/LanL2DZ and B3LYP/6311G+(d,p)) comparative vibrational spectroscopic analysis of organic-inorganic compound bis(4-acetylanilinium) tetrachlorocuprate(II)

    Science.gov (United States)

    Abkari, A.; Chaabane, I.; Guidara, K.

    2016-07-01

    The organic-inorganic salt, bis(4-acetylanilinium) tetrachlorocuprate(II), was synthesized and characterized by means of FT-IR (4000-400 cm-1) and Raman (3500-50 cm-1) in solid phase. The structure of [C8H10NO]2CuCl4 compound which was optimized by density functional theory (DFT) using B3LYP method showed that the calculated values obtained by B3LYP with LanL2DZ and 6311G+(d,p) basis sets are in better agreement with the experimental data. The computed vibrational frequencies were scaled by different scale factors to yield a good agreement with the experimental vibrational frequencies. The latter have been discussed on the basis of quantum chemical DFT calculations using the B3LYP/6311G+(d,p) and B3LYP/LanL2DZ method approach in gas phase. Besides, the effects due to the substitutions and the intermolecular interactions were investigated. The comparative analysis of the Raman spectra of the title compound with that of the free ligand was also discussed. The geometries and normal modes of the vibrations obtained from B3LYP/6311G+(d,p) calculation are found to be in good agreement with the experimentally observed data. The complete vibrational assignments and analysis of the observed fundamental bands of molecule were carried out.

  5. pH-resistant titania hybrid organic-inorganic sol-gel coating for solid-phase microextraction of polar compounds.

    Science.gov (United States)

    Li, Xiujuan; Gao, Jie; Zeng, Zhaorui

    2007-05-02

    A novel titania-hydroxy-terminated silicone oil (titania-OH-TSO) sol-gel coating was developed for solid-phase microextraction of polar compounds. In general, titania-based sol-gel reaction is very fast and need to be decelerated by the use of suitable chelating agents. But in the present work, a judiciously designed sol solution ingredients was used to create the titania-OH-TSO coating without the addition of any chelating agent, which simplified the sol-gel procedure. Thanks to the variety of titania's adsorption sites and their acid-base characteristics, aromatic amines, phenols and polycyclic aromatic hydrocarbons were efficiently extracted and preconcentrated from aqueous samples followed by thermal desorption and GC analysis. The newly developed sol-gel hybrid titania coating demonstrated excellent pH stability, and retained its extraction characteristics intact even after continuous rinsing with a 3 M HCl or NaOH solution for 12 h. Furthermore, it could withstand temperatures as high as 320 degrees C. Practical application was demonstrated through the analysis of six aromatic amines in dye process wastewater. A linearity of four orders of magnitude was obtained with correlation coefficient better than 0.9982. The detection limits ranged from 0.22 to 0.84 microg L(-1) and the repeatability of the measurements was <7.0%. The recoveries of these compounds studied in the wastewater were in the ranges 83.6-101.4%, indicating the method accuracy.

  6. Synthesis and Catalytic Applications of Non-Metal Doped Mesoporous Titania

    Directory of Open Access Journals (Sweden)

    Syed Z. Islam

    2017-03-01

    Full Text Available Mesoporous titania (mp-TiO2 has drawn tremendous attention for a diverse set of applications due to its high surface area, interfacial structure, and tunable combination of pore size, pore orientation, wall thickness, and pore connectivity. Its pore structure facilitates rapid diffusion of reactants and charge carriers to the photocatalytically active interface of TiO2. However, because the large band gap of TiO2 limits its ability to utilize visible light, non-metal doping has been extensively studied to tune the energy levels of TiO2. While first-principles calculations support the efficacy of this approach, it is challenging to efficiently introduce active non-metal dopants into the lattice of TiO2. This review surveys recent advances in the preparation of mp-TiO2 and their doping with non-metal atoms. Different doping strategies and dopant sources are discussed. Further, co-doping with combinations of non-metal dopants are discussed as strategies to reduce the band gap, improve photogenerated charge separation, and enhance visible light absorption. The improvements resulting from each doping strategy are discussed in light of potential changes in mesoporous architecture, dopant composition and chemical state, extent of band gap reduction, and improvement in photocatalytic activities. Finally, potential applications of non-metal-doped mp-TiO2 are explored in water splitting, CO2 reduction, and environmental remediation with visible light.

  7. 有机无机复混肥对无核白葡萄产量和果实品质的影响%Effect of Organic -inorganic Compound Fertilizer on the Yield and Quality of Thomson Seedless Grape

    Institute of Scientific and Technical Information of China (English)

    米热吉汗·阿不都热木; 齐曼·尤努斯; 玉山·库尔班; 艾克拜尔·伊拉洪; 谭建川

    2011-01-01

    [Objective] To study effects of different proportions organic - inorganic compound fertilizer on yield and quality of Turpan Thompson seedless grape, to provide theoretical and technical basis for scientific fertilization on Thompson seedless grape in this area. [Method] The 11 -years old Thompson Seedless grape was used as test materials. Four factors and 16 treatments were set in this experiment, and yield and several quality indexes were measured to determine the best formula of organic - inorganic compound fertilizer. [ Result ] After applying the different proportions of organic - inorganic compound fertilizer, the yield of 8 - 11 mus of proceed treatment was higher than that of the field by other treatments, among which the yields by treatment 10 and 11 were significantly higher than others, and the yields by treatment 1 and 16 were relatively lower; Treatments 9-12 have remarkable improvement effects on quality of Thompson seedless grapes; among them treatments 10 and 11 were the best formulas. After using fertilizer treatments 10 and 11, the 100 - grain weight, grain length and width, Vc content, soluble sugar and sugar - acid ratio of Thompson seedless grape were significantly higher than those by other formulations, and titration acid content was significantly lower than that by other treatments, while the hardness stayed at a high level. [ Conclusion]The organic - inorganiccompound fertilizer formulations 10 and 11 could significantly increase yield and quality of Thompson seedless grape, which have more popularization value in the area.%[目的]研究不同配比的有机无机复混肥对吐鲁番无核白葡萄产量、品质的影响,为该地区无核白葡萄的科学施肥提供理论技术依据.[方法]材料为11年生的无核白葡萄,实验设4个因素,16个处理,测定产量和几项品质指标,确定效果最佳的有机无机复混肥配方.[结果]施用不同配比的有机无机复混肥时,处理8~11的单产

  8. Fatigue Strength Prediction of Drilling Materials Based on the Maximum Non-metallic Inclusion Size

    Science.gov (United States)

    Zeng, Dezhi; Tian, Gang; Liu, Fei; Shi, Taihe; Zhang, Zhi; Hu, Junying; Liu, Wanying; Ouyang, Zhiying

    2015-12-01

    In this paper, the statistics of the size distribution of non-metallic inclusions in five drilling materials were performed. Based on the maximum non-metallic inclusion size, the fatigue strength of the drilling material was predicted. The sizes of non-metallic inclusions in drilling materials were observed to follow the inclusion size distribution rule. Then the maximum inclusion size in the fatigue specimens was deduced. According to the prediction equation of the maximum inclusion size and fatigue strength proposed by Murakami, fatigue strength of drilling materials was obtained. Moreover, fatigue strength was also measured through rotating bending tests. The predicted fatigue strength was significantly lower than the measured one. Therefore, according to the comparison results, the coefficients in the prediction equation were revised. The revised equation allowed the satisfactory prediction results of fatigue strength of drilling materials at the fatigue life of 107 rotations and could be used in the fast prediction of fatigue strength of drilling materials.

  9. Modelling of non-metallic particles motion process in foundry alloys

    Directory of Open Access Journals (Sweden)

    P. L. Żak

    2015-04-01

    Full Text Available The behaviour of non-metallic particles in the selected composites was analysed, in the current study. The calculations of particles floating in liquids differing in viscosity were performed. Simulations based on the Stokes equation were made for spherical SiC particles and additionally the particle size influence on Reynolds number was analysed.The movement of the particles in the liquid metal matrix is strictly connected with the agglomerate formation problem.Some of collisions between non-metallic particles lead to a permanent connection between them. Creation of the two spherical particles and a metallic phase system generates the adhesion force. It was found that the adhesion force mainly depends on the surface tension of the liquid alloy and radius of non-metallic particles.

  10. The Effect of Different Non-Metallic Inclusions on the Machinability of Steels.

    Science.gov (United States)

    Ånmark, Niclas; Karasev, Andrey; Jönsson, Pär Göran

    2015-02-16

    Considerable research has been conducted over recent decades on the role of non‑metallic inclusions and their link to the machinability of different steels. The present work reviews the mechanisms of steel fractures during different mechanical machining operations and the behavior of various non-metallic inclusions in a cutting zone. More specifically, the effects of composition, size, number and morphology of inclusions on machinability factors (such as cutting tool wear, power consumption, etc.) are discussed and summarized. Finally, some methods for modification of non-metallic inclusions in the liquid steel are considered to obtain a desired balance between mechanical properties and machinability of various steel grades.

  11. Modification of Non-Metallic Inclusions by Rare-Earth Elements in Microalloyed Steels

    OpenAIRE

    Opiela M.; Grajcar A.

    2012-01-01

    The modification of the chemical composition of non-metallic inclusions by rare-earth elements in the new-developed microalloyed steels was discussed in the paper. The investigated steels are assigned to production of forged elements by thermo- mechanical treatment. The steels were melted in a vaccum induction furnace and modification of non-metallic inclusions was carried out by the michmetal in the amount of 2.0 g per 1 kg of steel. It was found that using material charge of high purity and...

  12. The Effect of Different Non-Metallic Inclusions on the Machinability of Steels

    Directory of Open Access Journals (Sweden)

    Niclas Ånmark

    2015-02-01

    Full Text Available Considerable research has been conducted over recent decades on the role of non‑metallic inclusions and their link to the machinability of different steels. The present work reviews the mechanisms of steel fractures during different mechanical machining operations and the behavior of various non-metallic inclusions in a cutting zone. More specifically, the effects of composition, size, number and morphology of inclusions on machinability factors (such as cutting tool wear, power consumption, etc. are discussed and summarized. Finally, some methods for modification of non-metallic inclusions in the liquid steel are considered to obtain a desired balance between mechanical properties and machinability of various steel grades.

  13. Copper inorganic-organic hybrid coordination compound as a novel L-cysteine electrochemical sensor: Synthesis, characterization, spectroscopy and crystal structure

    Indian Academy of Sciences (India)

    Zohreh Derikvand; Azadeh Azadbakht

    2015-11-01

    Dinuclear coordination compound of Cu(II), namely, [Cu2(pydc)2(pz)(H2O)2]·2H2O, where pydc = pyridine-2,6-dicarboxylic acid (dipicolinic acid) and pz = pyrazine has been synthesized and characterized by elemental analysis, spectra (IR, UV-Vis), thermal (TG/DTG) analysis, magnetic measurements and single crystal X-ray diffraction. In the dimeric structure, the planar tridentate pyridine-2,6-dicarboxylic acid dianion coordinates to a Cu(II) ion in a meridional fashion and defines the basal plane of the complex. The fourth equatorial coordination site is then occupied by a pyrazine molecule that functions as a linear bidentate ligand bridging two Cu(II) complexes to form a dimer. The axial positions of each Cu(II) complex are occupied by one water molecule to form a distorted square pyramidal geometry. The complicated hydrogen bonding network accompanied with C–O· · · and C–H· · · stacking interactions assemble the crystal structure of 1 into a fascinating supramolecular architecture. Electrochemical behavior of [Cu2(pydc)2(pz)(H2O)2] (Cu-PDAP) on the surface of carbon nanotube (CNTs) glassy carbon electrode (GCE) is described. Oxidation of cysteine on the surface of modified electrode was investigated with cyclic voltammetry and electrochemical impedance spectroscopy (EIS). The results show that the Cu-PDAP/CNTs film displays excellent electrochemical catalytic activities towards L-cysteine oxidation.

  14. Alternative current conduction mechanisms of organic-inorganic compound [N(CH3)3H]2CuCl4

    Science.gov (United States)

    Ben Bechir, M.; Karoui, K.; Tabellout, M.; Guidara, K.; Ben Rhaiem, A.

    2014-05-01

    The [N(CH3)3H]2CuCl4 single crystal has been analyzed by X-ray powder diffraction patterns, differential scanning calorimetry (DSC), and electrical impedance spectroscopy. [N(CH3)3H]2CuCl4 crystallizes at room temperature in the monoclinic system with P21/C space group. Three phase transitions at T1 = 226 K, T2 = 264 K, and T3 = 297 K have been evidenced by DSC measurements. The electrical technique was measured in the 10-1-107 Hz frequency range and 203-313 K temperature intervals. The frequency dependence of alternative current (AC) conductivity is interpreted in terms of Jonscher's law (developed). The AC electrical conduction in [N(CH3)3H]2CuCl4 compound is studied by two processes which can be attributed to a hopping transport mechanism: the correlated barrier hopping model in phases I, II, and III, the non-overlapping small polaron tunneling model in phase IV. The conduction mechanism is interpreted with the help of Elliot's theory, and the Elliot's parameters are found.

  15. 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.

  16. Synthesis, crystal structures and characterization of two novel organic-inorganic hybrid compounds (C5NH6)6Bi4Br18 and [C(NH2)3]3BiI6

    Science.gov (United States)

    Li, S. G.; Chen, L.; Xiang, Y.

    2017-02-01

    Two novel organic-inorganic compounds (C5NH6)6Bi4Br18 (1) and [C(NH2)3]3BiI6 (2) have been synthesized and characterized by elemental analysis, measured by DSC and single-crystal X-ray diffraction at room temperature. The crystal structure of (1) crystallizes in the monoclinic space group C2/m, with a = 17.12 (3), b = 15.3939 (1), c = 13.412 (2) Å, β = 123.702 (7)°, V = 3042.2 (8) Å3 and Z = 2. The crystal structure consists of discrete quad-core [Bi4Br18]6- anions and [C5NH6]+ cations. 2 crystallizes in triclinic space group P-1, with the following unit cell parameters: a = 9.3435 (2), b = 15.583 (4), c = 17.200 (4) Å, α = 86.383 (1), β = 75.689 (1), γ = 89.918 (6)°, V = 2421.5 (10) Å3 and Z = 4. The crystal lattice is composed of discrete [BiI6]3- anions surrounded by [C(NH2)3]+ cations. The DSC experiment of 1 clearly displays that a phase transition occurred at 124.7 K, while 2 undergoes a phase transition at 192.5 K.

  17. Supramolecular hydrogen-bonding patterns in the organic-inorganic hybrid compound bis(4-amino-5-chloro-2,6-dimethylpyrimidinium) tetrathiocyanatozinc(II)-4-amino-5-chloro-2,6-dimethylpyrimidine-water (1/2/2).

    Science.gov (United States)

    Karthikeyan, Ammasai; Zeller, Matthias; Thomas Muthiah, Packianathan

    2016-04-01

    Zinc thiocyanate complexes have been found to be biologically active compounds. Zinc is also an essential element for the normal function of most organisms and is the main constituent in a number of metalloenzyme proteins. Pyrimidine and aminopyrimidine derivatives are biologically very important as they are components of nucleic acids. Thiocyanate ions can bridge metal ions by employing both their N and S atoms for coordination. They can play an important role in assembling different coordination structures and yield an interesting variety of one-, two- and three-dimensional polymeric metal-thiocyanate supramolecular frameworks. The structure of a new zinc thiocyanate-aminopyrimidine organic-inorganic compound, (C6H9ClN3)2[Zn(NCS)4]·2C6H8ClN3·2H2O, is reported. The asymmetric unit consist of half a tetrathiocyanatozinc(II) dianion, an uncoordinated 4-amino-5-chloro-2,6-dimethylpyrimidinium cation, a 4-amino-5-chloro-2,6-dimethylpyrimidine molecule and a water molecule. The Zn(II) atom adopts a distorted tetrahedral coordination geometry and is coordinated by four N atoms from the thiocyanate anions. The Zn(II) atom is located on a special position (twofold axis of symmetry). The pyrimidinium cation and the pyrimidine molecule are not coordinated to the Zn(II) atom, but are hydrogen bonded to the uncoordinated water molecules and the metal-coordinated thiocyanate ligands. The pyrimidine molecules and pyrimidinium cations also form base-pair-like structures with an R2(2)(8) ring motif via N-H...N hydrogen bonds. The crystal structure is further stabilized by intermolecular N-H...O, O-H...S, N-H...S and O-H...N hydrogen bonds, by intramolecular N-H...Cl and C-H...Cl hydrogen bonds, and also by π-π stacking interactions.

  18. 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...

  19. Stepped-Frequency Ground-Penetrating Radar for Detection of Small Non-metallic Buried Objects

    DEFF Research Database (Denmark)

    Jakobsen, Kaj Bjarne; Sørensen, Helge Bjarup Dissing; Nymann, Ole

    1997-01-01

    A monostatic amplitude and phase stepped-frequency radar approach have been proposed to detect small non-metallic buried anti-personnel (AP) mines. An M-56 AP-mine with a diameter of 54 mm and height of 40 mm, only, has been successfully detected and located in addition to small metallic mine...

  20. Soil effects on GPR detection of buried non-metallic mines

    NARCIS (Netherlands)

    Hendrickx, J.M.H.; Hong, S.H.; Miller, T.; Borchers, B.; Rhebergen, J.B.

    2003-01-01

    Landmines are a major problem in many areas of the world. In spite of the fact that many different types of landmine sensors have been developed, the detection of non-metallic landmines remains very difficult. The objective of this contribution is to synthesize our work related to the effects of soi

  1. The Measurement of Hardness and Elastic Modulus of non-Metallic Inclusions in Steely Welding Joints

    Directory of Open Access Journals (Sweden)

    Ignatova Anna

    2015-08-01

    Full Text Available Trunk pipelines work under a cyclic dynamical mechanical load because when oil or gas is pumped, the pressure constantly changes - pulsates. Therefore, the fatigue phenomenon is a common reason of accidents. The fatigue phenomenon more often happens in the zone of non-metallic inclusions concentration. To know how the characteristics of nonmetallic inclusions influence the probability of an accident the most modern research methods should be used. It is determined with the help of the modern research methods that the accident rate of welded joints of pipelines is mostly influenced by their morphological type, composition and size of nonmetallic inclusions, this effect is more important than the common level of pollution by non-metallic inclusions. The article presents the results of the investigations of welded joints, obtained after the use of different common welding materials. We used the methods, described in the state standards: scanning electronic microscopy, spectral microprobe analysis and nano-indentation. We found out that non-metallic inclusions act like stress concentrators because they shrink, forming a blank space between metal and nonmetallic inclusions; it strengthens the differential properties on this boundary. Nonmetallic inclusion is not fixed, it can move. The data that we have received mean that during welded joints’ contamination (with non-metallic inclusions monitoring process, more attention should be paid to the content of definite inclusions, but not to total contamination.

  2. Size of Non-Metallic Inclusions in High-Grade Medium Carbon Steel

    Directory of Open Access Journals (Sweden)

    Lipiński T.

    2014-12-01

    Full Text Available Non-metallic inclusions found in steel can affect its performance characteristics. Their impact depends not only on their quality, but also, among others, on their size and distribution in the steel volume. The literature mainly describes the results of tests on hard steels, particularly bearing steels. The amount of non-metallic inclusions found in steel with a medium carbon content melted under industrial conditions is rarely presented in the literature. The tested steel was melted in an electric arc furnace and then desulfurized and argonrefined. Seven typical industrial melts were analyzed, in which ca. 75% secondary raw materials were used. The amount of non-metallic inclusions was determined by optical and extraction methods. The test results are presented using stereometric indices. Inclusions are characterized by measuring ranges. The chemical composition of steel and contents of inclusions in every melts are presented. The results are shown in graphical form. The presented analysis of the tests results on the amount and size of non-metallic inclusions can be used to assess them operational strength and durability of steel melted and refined in the desulfurization and argon refining processes.

  3. Assessment of ethylene dibromide, dibromochloropropane, other volatile organic compounds, radium isotopes, radon, and inorganic compounds in groundwater and spring water from the Crouch Branch and McQueen Branch aquifers near McBee, South Carolina, 2010-2012

    Science.gov (United States)

    Landmeyer, James E.; Campbell, Bruce G.

    2014-01-01

    Public-supply wells near the rural town of McBee, in southwestern Chesterfield County, South Carolina, have provided potable water to more than 35,000 residents throughout Chesterfield County since the early 1990s. Groundwater samples collected between 2002 and 2008 in the McBee area by South Carolina Department of Health and Environmental Control (DHEC) officials indicated that groundwater from two public-supply wells was characterized by the anthropogenic compounds ethylene dibromide (EDB) and dibromochloropropane (DBCP) at concentrations that exceeded their respective maximum contaminant levels (MCLs) established by the U.S. Environmental Protection Agency’s (EPA) National Primary Drinking Water Regulations (NPDWR). Groundwater samples from all public-supply wells in the McBee area were characterized by the naturally occurring isotopes of radium-226 and radium-228 at concentrations that approached, and in one well exceeded, the MCL for the combined isotopes. The local water utility installed granulated activated carbon filtration units at the two EDB- and DBCP-contaminated wells and has, since 2011, shut down these two wells. Groundwater pumped by the remaining public-supply wells is currently (2014) centrally treated at a water-filtration plant.

  4. Inorganic-organic hybrid white light phosphors.

    Science.gov (United States)

    Wang, Ming-Sheng; Guo, Guo-Cong

    2016-11-03

    Light-emitting diodes (LEDs) and organic light-emitting diodes (OLEDs) have brought about a revolution in lighting and display. A very hot field in recent years has been to develop white-light phosphors, aiming to achieve better colour stability, better reproducibility, and a simpler fabrication process for LEDs and OLEDs. This feature article reviews the development of inorganic-organic hybrid white-light phosphors, including coordination compounds of small organic molecules, organically templated inorganic compounds (phosphates, borates, sulfides, halides), metal-functionalized organic polymers, and organically coated nanoparticles.

  5. Inorganic semiconductors for flexible electronics.

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Y.; Rogers, J. A.; Center for Nanoscale Materials; Univ. of Illinois

    2007-08-03

    This article reviews several classes of inorganic semiconductor materials that can be used to form high-performance thin-film transistors (TFTs) for large area, flexible electronics. Examples ranging from thin films of various forms of silicon to nanoparticles and nanowires of compound semiconductors are presented, with an emphasis on methods of depositing and integrating thin films of these materials into devices. Performance characteristics, including both electrical and mechanical behavior, for isolated transistors as well as circuits with various levels of complexity are reviewed. Collectively, the results suggest that flexible or printable inorganic materials may be attractive for a range of applications not only in flexible but also in large-area electronics, from existing devices such as flat-panel displays to more challenging (in terms of both cost and performance requirements) systems such as large area radiofrequency communication devices, structural health monitors, and conformal X-ray imagers.

  6. Prediction of activity coefficients in liquid aerosol particles containing organic compounds, dissolved inorganic salts, and water—Part 2: Consideration of phase separation effects by an X-UNIFAC model

    Science.gov (United States)

    Chang, Elsa I.; Pankow, James F.

    A thermodynamic model is presented for predicting the formation of particulate matter (PM) within an aerosol that contains organic compounds, inorganic salts, and water. Neutral components are allowed to partition from the gas phase to the PM, with the latter potentially composed of both a primarily aqueous ( α) liquid phase and a primarily organic ( β) liquid phase. Partitioning is allowed to occur without any artificial restraints: when both α and β PM phases are present, ionic constituents are allowed to partition to both. X-UNIFAC.2, an extended UNIFAC method based on Yan et al. (1999. Prediction of vapor-liquid equilibria in mixed-solvent electrolyte systems using the group contribution concept. Fluid Phase Equilibria 162, 97-113), was developed for activity coefficient estimation. X-UNIFAC.2 utilizes the standard UNIFAC terms, a Debye-Hückel term, and a virial equation term that represents the middle-range (MR) contribution to activity coefficient effects. A large number (234) of MR parameters are already available from Yan et al. (1999). Six additional MR parameters were optimized here to enable X-UNIFAC.2 to account for interactions between the carboxylic acid group and Na +, Cl -, and Ca 2+. Predictions of PM formation were made for a hypothetical sabinene/O 3 system with varying amounts of NaCl in the PM. Predictions were also made for the chamber experiments with α-pinene/O 3 (and CaCl 2 seed) carried out by Cocker et al. (2001. The effect of water on gas-particle partitioning of secondary organic aerosol. Part I. α-pinene/ozone system. Atmospheric Environment 35, 6049-6072); good agreement between the predicted and chamber-measured PM mass concentrations was achieved.

  7. 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。

  8. The Global Redox Responding RegB/RegA Signal Transduction System Regulates the Genes Involved in Ferrous Iron and Inorganic Sulfur Compound Oxidation of the Acidophilic Acidithiobacillus ferrooxidans

    Directory of Open Access Journals (Sweden)

    Danielle Moinier

    2017-07-01

    Full Text Available The chemical attack of ore by ferric iron and/or sulfuric acid releases valuable metals. The products of these reactions are recycled by iron and sulfur oxidizing microorganisms. These acidophilic chemolithotrophic prokaryotes, among which Acidithiobacillus ferrooxidans, grow at the expense of the energy released from the oxidation of ferrous iron and/or inorganic sulfur compounds (ISCs. In At. ferrooxidans, it has been shown that the expression of the genes encoding the proteins involved in these respiratory pathways is dependent on the electron donor and that the genes involved in iron oxidation are expressed before those responsible for ISCs oxidation when both iron and sulfur are present. Since the redox potential increases during iron oxidation but remains stable during sulfur oxidation, we have put forward the hypothesis that the global redox responding two components system RegB/RegA is involved in this regulation. To understand the mechanism of this system and its role in the regulation of the aerobic respiratory pathways in At. ferrooxidans, the binding of different forms of RegA (DNA binding domain, wild-type, unphosphorylated and phosphorylated-like forms of RegA on the regulatory region of different genes/operons involved in ferrous iron and ISC oxidation has been analyzed. We have shown that the four RegA forms are able to bind specifically the upstream region of these genes. Interestingly, the phosphorylation of RegA did not change its affinity for its cognate DNA. The transcriptional start site of these genes/operons has been determined. In most cases, the RegA binding site(s was (were located upstream from the −35 (or −24 box suggesting that RegA does not interfere with the RNA polymerase binding. Based on the results presented in this report, the role of the RegB/RegA system in the regulation of the ferrous iron and ISC oxidation pathways in At. ferrooxidans is discussed.

  9. The Global Redox Responding RegB/RegA Signal Transduction System Regulates the Genes Involved in Ferrous Iron and Inorganic Sulfur Compound Oxidation of the Acidophilic Acidithiobacillus ferrooxidans.

    Science.gov (United States)

    Moinier, Danielle; Byrne, Deborah; Amouric, Agnès; Bonnefoy, Violaine

    2017-01-01

    The chemical attack of ore by ferric iron and/or sulfuric acid releases valuable metals. The products of these reactions are recycled by iron and sulfur oxidizing microorganisms. These acidophilic chemolithotrophic prokaryotes, among which Acidithiobacillus ferrooxidans, grow at the expense of the energy released from the oxidation of ferrous iron and/or inorganic sulfur compounds (ISCs). In At. ferrooxidans, it has been shown that the expression of the genes encoding the proteins involved in these respiratory pathways is dependent on the electron donor and that the genes involved in iron oxidation are expressed before those responsible for ISCs oxidation when both iron and sulfur are present. Since the redox potential increases during iron oxidation but remains stable during sulfur oxidation, we have put forward the hypothesis that the global redox responding two components system RegB/RegA is involved in this regulation. To understand the mechanism of this system and its role in the regulation of the aerobic respiratory pathways in At. ferrooxidans, the binding of different forms of RegA (DNA binding domain, wild-type, unphosphorylated and phosphorylated-like forms of RegA) on the regulatory region of different genes/operons involved in ferrous iron and ISC oxidation has been analyzed. We have shown that the four RegA forms are able to bind specifically the upstream region of these genes. Interestingly, the phosphorylation of RegA did not change its affinity for its cognate DNA. The transcriptional start site of these genes/operons has been determined. In most cases, the RegA binding site(s) was (were) located upstream from the -35 (or -24) box suggesting that RegA does not interfere with the RNA polymerase binding. Based on the results presented in this report, the role of the RegB/RegA system in the regulation of the ferrous iron and ISC oxidation pathways in At. ferrooxidans is discussed.

  10. Stereochemistry of organometallic and inorganic compounds

    CERN Document Server

    2012-01-01

    The authors of this fourth volume in the series have reviewed the making and breaking of chemical bonds in a sophisticated manner. In particular, new pressures brought about by environmental concerns, larger demands for the medical and pharmaceutical sectors and economics of the market place are forcing us into demanding greater stereochemical control and better product yields for chemical reactions capable of producing useful products. The chapters are written by leading experts in this area and give excellent overviews of the strengths and weaknesses of the various methodologies.In C

  11. The mineral base and productive capacities of metals and non-metals of Kosovo

    Energy Technology Data Exchange (ETDEWEB)

    Rizaj, M.; Beqiri, E.; McBow, I.; O' Brien, E.Z.; Kongoli, F. [University of Prishtina, Prishtina (Kosovo)

    2008-08-15

    All historical periods of Kosovo - Ilirik, Roman, Medieval, Turkish, and former Yugoslavian - are linked with the intensive development of mining and metallurgy. This activity influenced and still is influencing the overall position of Kosovo as a country. For example, according to a 2006 World Bank report as well as other studies, Kosovo has potential lignite resources (geological reserves) of about 1.5 billion tonnes, which are ranked fifth in the world in importance. Other significant Kosovan mineral resources include lead, zinc, gold, silver, bauxite, and uranium, and rare metals accompanying those minerals, including indium, cadmium, thallium, gallium, and bismuth. These rare metals are of particular importance in developing advanced industrial technologies. Kosovo also has reserves of high-quality non-metals, including magnesite, quartz grit, bentonite, argil, talc, and asbestos. No database exists for these non-metal reserves, and further research and studies are needed.

  12. The mineral base and productive capacities of metals and non-metals of Kosovo

    Science.gov (United States)

    Rizaj, M.; Beqiri, E.; McBow, I.; O'Brien, E. Z.; Kongoli, F.

    2008-08-01

    All historical periods of Kosovo—Ilirik, Roman, Medieval, Turkish, and former Yugoslavian—are linked with the intensive development of mining and metallurgy. This activity influenced and still is influencing the overall position of Kosovo as a country. For example, according to a 2006 World Bank report as well as other studies, Kosovo has potential lignite resources (geological reserves) of about 1.5 billion tonnes, which are ranked fifth in the world in importance. Other significant Kosovan mineral resources include lead, zinc, gold, silver, bauxite, and uranium, and rare metals accompanying those minerals, including indium, cadmium, thallium, gallium, and bismuth. These rare metals are of particular importance in developing advanced industrial technologies. Kosovo also has reserves of high-quality non-metals, including magnesite, quartz grit, bentonite, argil, talc, and asbestos. No database exists for these non-metal reserves, and further research and studies are needed.

  13. Computer Simulation of the Formation of Non-Metallic Precipitates During a Continuous Casting of Steel

    Directory of Open Access Journals (Sweden)

    Kalisz D.

    2016-03-01

    Full Text Available The authors own computer software, based on the Ueshima mathematical model with taking into account the back diffusion, determined from the Wołczyński equation, was developed for simulation calculations. The applied calculation procedure allowed to determine the chemical composition of the non-metallic phase in steel deoxidised by means of Mn, Si and Al, at the given cooling rate. The calculation results were confirmed by the analysis of samples taken from the determined areas of the cast ingot. This indicates that the developed computer software can be applied for designing the steel casting process of the strictly determined chemical composition and for obtaining the required non-metallic precipitates.

  14. Non-metallic catalysts for diamond synthesis under high pressure and high temperature

    Institute of Scientific and Technical Information of China (English)

    孙力玲; 吴奇; 戴道扬; 张君; 秦志成; 王文魁

    1999-01-01

    Recent results on conversion from graphite to diamond by aid of non-metallic catalysts are reviewed. The current status of experimental advances is presented and typical examples from relevant literature are provided for understanding the mechanism of the graphite-diamond conversion by aid of these non-metallic catalysts. Furthermore, a tendency of graphite-diamond transformation assisted by carbonates, sulfates or phosphorus under high pressure and high temperature has been investigated by calculating the activation energy and transformation probability of the carbon atoms over a potential barrier. It was found that the activation energy is highly sensitive to the catalyst chosen. The probability sequence of graphite-diamond transformation with these catalysts was put forward.

  15. Motion behavior of non-metallic particles under high frequency magnetic field

    Institute of Scientific and Technical Information of China (English)

    ZHANG Zhong-tao; GUO Qing-tao; YU Feng-yun; LI Jie; ZHANG Jian; LI Ting-ju

    2009-01-01

    Non-metallic particles, especially alumina, are the main inclusions in aluminum and its alloys. Numerical simulation and the corresponding experiments were carried out to study the motion behavior of alumina particles in commercial pure aluminum under high frequency magnetic field. At the meantime, multi-pipe experiment was also done to discuss the prospect of continuous elimination of non-metallic particles under high frequency magnetic field. It is shown that: 1) results of numerical simulation are in good agreement with the experimental results, which certificates the rationality of the simulation model; 2) when the intensity of high frequency magnetic field is 0.06 T, the 30 μm alumina particles in melt inner could migrate to the edge and be removed within 2 s; 3) multi-pipe elimination of alumina particles under high frequency magnetic field is also effective and has a good prospect in industrial application.

  16. Color stability, water sorption and cytotoxicity of thermoplastic acrylic resin for non metal clasp denture

    OpenAIRE

    Jang, Dae-Eun; Lee, Ji-Young; Jang, Hyun-Seon; Lee, Jang-Jae; Son, Mee-Kyoung

    2015-01-01

    PURPOSE The aim of this study was to compare the color stability, water sorption and cytotoxicity of thermoplastic acrylic resin for the non-metal clasp dentures to those of thermoplastic polyamide and conventional heat-polymerized denture base resins. MATERIALS AND METHODS Three types of denture base resin, which are conventional heat-polymerized acrylic resin (Paladent 20), thermoplastic polyamide resin (Bio Tone), thermoplastic acrylic resin (Acrytone) were used as materials for this study...

  17. NON-METALLIC IMPURITIES AND FORMING OF THE STRUCTURE OF THE MODIFIED HIGH-MANGANESE STEEL

    Directory of Open Access Journals (Sweden)

    A. I. Garost

    2006-01-01

    Full Text Available The composition and morphology of chemical associations (non-metallic impurities and other ‘‘secondary” phases at modification of high-manganese steel by nitrogen and nitrideforming elements (vanadium are investigated. The optimal compositions of steel for production of castings are offered. The technology of the steel wear-resistance modification by vanadium of waste of industrial enterprises is worked out.

  18. Behavior of Non-metallic Inclusions in Centrifugal Induction Electroslag Castings

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    (para)In order to know the behavior of non-metallic inclusions in centrifugal induction electroslag castings (CIESC), non-metallic inclusions in 5CrMnMo and 4Cr5MoSiV1 were qualitatively and quantitatively analyzed. The largest size of inclusions in the casting and the thermodynamic possibility of TiN precipitation in steel were also calculated. The results show that sulfide inclusions are evenly distributed and the content is low. The amount of oxide inclusions in CIESC 4Cr5MoSiV1 steel is close to the ESR steel and lower than that in the EAF steel, and there are some differences along radial direction. Nitride inclusions are fine and the diameter of the largest one is 3~4um. With the increase of the centrifugal machine's rotational speed, the ratio of round inclusions increases and the ratio of sharp inclusions decreases. According to the experiment and the calculation results, it is pointed out that the largest diameter of non-metallic inclusions in the CIESC 4Cr5MoSiV1 casting is only 6.6mu, and [N%][Ti%] in 4Cr5MoSiV1 steel should be controlled less than 4.4~#U00d7tex010^{-5} in order to further reduce the amount and size of TiN inclusions.

  19. Evaluation of Characteristics of Non-Metallic Inclusions in P/M Ni-Base Superalloy by Automatic Image Analysis

    Institute of Scientific and Technical Information of China (English)

    Li; Xinggang; Ge; Changchun; Shen; Weiping

    2007-01-01

    Non-metallic inclusions,especially the large ones,within P/M Ni-base superalloy have a major influence on fatigue characteristics,but are not directly measurable by routine inspection.In this paper,a method,automatic image analysis,is proposed for estimation of the content,size and amount of non-metallic inclusions in superalloy.The methodology for the practical application of this method is described and the factors affecting the precision of the estimation are discussed.In the experiment,the characteristics of the non-metallic inclusions in Ni-base P/M superalloy are analyzed.

  20. Modelling inorganic material in activated sludge systems

    African Journals Online (AJOL)

    driniev

    2004-04-02

    Apr 2, 2004 ... organic models above, predictive models for the reactor inorganic ... included TSS as a non-conservative compound (Gujer and Lawson,. 1995) .... The OHO and PAO fractions of the VSS (favOHO, favPAO) are defined by, and ...

  1. Synthesis and structure of dawson polyoxometalate-based, multifunctional, inorganic-organic hybrid compounds: organogermyl complexes with one terminal functional group and organosilyl analogues with two terminal functional groups.

    Science.gov (United States)

    Nomiya, Kenji; Togashi, Yoshihiro; Kasahara, Yuhki; Aoki, Shotaro; Seki, Hideaki; Noguchi, Marie; Yoshida, Shoko

    2011-10-03

    Four novel multifunctional polyoxometalate (POM)-based inorganic-organic hybrid compounds, [α(2)-P(2)W(17)O(61){(RGe)}](7-) (Ge-1, R(1) = HOOC(CH(2))(2(-)) and Ge-2, R(2) = H(2)C═CHCH(2(-))) and [α(2)-P(2)W(17)O(61){(RSi)(2)O}](6-) (Si-1, R(1) and Si-2, R(2)), were prepared by incorporating organic chains having terminal functional groups (carboxylic acid and allyl groups) into monolacunary site of Dawson polyoxoanion [α(2)-P(2)W(17)O(61)](10-). In these POMs, new modification of the terminal functional groups was attained by introducing organogermyl and organosilyl groups. Dimethylammonium salts of the organogermyl complexes, (Me(2)NH(2))(7)[α(2)-P(2)W(17)O(61)(R(1)Ge)]·H(2)O MeN-Ge-1 and (Me(2)NH(2))(7)[α(2)-P(2)W(17)O(61)(R(2)Ge)]·4H(2)O MeN-Ge-2, were obtained as analytically pure crystals, in 22.8% and 55.3% yields, respectively, by stoichiometric reactions of [α(2)-P(2)W(17)O(61)](10-) with separately prepared Cl(3)GeC(2)H(4)COOH in water, and H(2)C═CHCH(2)GeCl(3) in a solvent mixture of water/acetonitrile. Synthesis and X-ray structure analysis of the Dawson POM-based organogermyl complexes were first successful. Dimethylammonium salts of the corresponding organosilyl complexes, (Me(2)NH(2))(6)[α(2)-P(2)W(17)O(61){(R(1)Si)(2)O}]·4H(2)O MeN-Si-1 and (Me(2)NH(2))(6)[α(2)-P(2)W(17)O(61){(R(2)Si)(2)O}]·6H(2)O MeN-Si-2, were also obtained as analytically pure crystalline crystals, in 17.1% and 63.5% yields, respectively, by stoichiometric reactions of [α(2)-P(2)W(17)O(61)](10-) with NaOOC(CH(2))(2)Si(OH)(2)(ONa) and H(2)C═CHCH(2)Si(OEt)(3). These complexes were characterized by elemental analysis, thermogravimetric and differential thermal analyses (TG/DTA), FTIR, solid-state ((31)P) and solution ((31)P, (1)H, and (13)C) NMR, and X-ray crystallography.

  2. Synthesis, characterization, single crystal X-ray structure, EPR and theoretical studies of a new hybrid inorganic-organic compound [Cu(Hdien)2(H2O)2](pnb)4·4H2O and its structural comparison with related [Cu(en)2(H2O)2](pnb)2

    Science.gov (United States)

    Kumar, Santosh; Sharma, Raj Pal; Venugopalan, Paloth; Witwicki, Maciej; Ferretti, Valeria

    2016-11-01

    A new hybrid inorganic-organic compound [Cu(Hdien)2(H2O)2](pnb)4·4H2O (1) (where pnb = p-nitrobenzoate), in which the tridentate ligand diethylenetriamine (dien) shows an unusual coordination behavior acting as a bidentate ligand when present in its monoprotonated form (Hdien+) has been synthesized by the reaction of copper(II) p-nitrobenzoate and slight excess of dien in methanol-water mixture (4:1v/v). Re-crystallization of the violet precipitated product from hot water gave single crystals suitable for X-ray diffraction studies. The newly synthesized compound 1 has been characterized by spectroscopic techniques (UV-Vis, FT-IR, EPR), and theoretical methods (DFT and MRCI/SORCI). Single crystal X-ray structure determination revealed the existence of the cationic species [Cu(Hdien)2(H2O)2]4+, four p-nitrobenzoate as counter anions and four water molecules are present as solvent of crystallization. Packing analyses of title compound as well as of the structurally similar [Cu(en)2(H2O)2](pnb)2,2 has shown similarities in the crystalline architecture that both hybrid inorganic-organic compounds is stabilized by various non-covalent interactions such as N-H⋯O, C-H⋯O, O-H⋯O etc.

  3. 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

  4. Organic-Inorganic Composites Toward Biomaterial Application.

    Science.gov (United States)

    Miyazaki, Toshiki; Sugawara-Narutaki, Ayae; Ohtsuki, Chikara

    2015-01-01

    Bioactive ceramics are known to exhibit specific biological affinities and are able to show direct integration with surrounding bone when implanted in bony defects. However, their inadequate mechanical properties, such as low fracture toughness and high Young's modulus in comparison to natural bone, limit their clinical application. Bone is a kind of organic-inorganic composite where apatite nanocrystals are precipitated onto collagen fibre networks. Thus, one way to address these problems is to mimic the natural composition of bone by using bioactive ceramics via material designs based on organic-inorganic composites. In this chapter, the current research on the development of the various organic-inorganic composites designed for biomaterial applications has been reviewed. Various compounds such as calcium phosphate, calcium sulphate and calcium carbonate can be used for the inorganic phases to design composites with the desired mechanical and biological properties of bone. Not only classical mechanical mixing but also coating of the inorganic phase in aqueous conditions is available for the fabrication of such composites. Organic modifications using various polymers enable the control of the crystalline structure of the calcium carbonate in the composites. These approaches on the fabrication of organic-inorganic composites provide important options for biomedical materials with novel functions. © 2015 S. Karger AG, Basel.

  5. 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.

  6. 有机无机杂化物作乳化剂的苯丙乳液制备及其性能表征%Synthesis and Characterization of Poly(St-co-BA) Latex with an Organic-Inorganic Hybrid Compound as Emulsifier

    Institute of Scientific and Technical Information of China (English)

    袁俊杰; 周树学; 廖建和; 武利民

    2003-01-01

    A poly (St-co-BA) latex was successfully synthesized by using an organic-inorganic hybrid compound(OIHC), an aliphatic carboxylate sodium/nano-silica composite, as the emulsifier, and investigated by particlesize analyzer, transmission electron microscope (TEM), optical contact angle measurement (OCA) and dynamicmechanical analyzer (DMA). It was found that the protective agent, sodium polyacrylate (PA),could obviouslyimprove the polymerization stability and the functional monomer, glycidyl methacrylate (GMA), could enhancethe store stability of the latex. The particle size of poly(St-co-BA) latex decreased and then leveled off as OIHCcontent increased. TEM shows that the prepared polymers were actually organic-inorganic nanocomposites, andthese films have better waterproof property than those prepared by traditional poly(St-co-BA) latex or organicsilicone modified poly(St-co-BA) latex. The nanocomposite polymer has much higher glass transition temperaturethan organic silicone modified poly(St-co-BA) polymer containing the same organic silicone content.

  7. Polyoxometalate (POM)-based, multi-functional, inorganic-organic, hybrid compounds: syntheses and molecular structures of silanol- and/or siloxane bond-containing species grafted on mono- and tri-lacunary Keggin POMs.

    Science.gov (United States)

    Aoki, Shotaro; Kurashina, Takayuki; Kasahara, Yuhki; Nishijima, Tadashi; Nomiya, Kenji

    2011-02-14

    Using 3-mercaptopropyltrimethoxysilane (HS(CH₂)₃Si(OMe)₃) as a silane-coupling agent (SCA), mono- and tri-lacunary Keggin polyoxometalate (POM)-based, multi-functional, inorganic-organic, hybrid compounds, (Et₄N)₃[α-PW₁₁O₃₉{(HS(CH₂)₃Si)₂O}] EtN-1 (the 1 : 2 complex of a POM unit and organosilyl groups), (Bu₄N)₃[A-PW₉O₃₄(HS(CH₂)₃SiOH)₃] BuN-2 (the 1 : 3 complex) and (Bu₄N)₃[A-α-PW₉O₃₄(HS(CH₂)₃SiO)₃(Si(CH₂)₃SH)] BuN-3 (the 1 : 4 complex) were synthesized and unequivocally characterized by elemental analysis, thermogravimetric and differential thermal analyses (TG/DTA), FTIR, solid-state (²⁹Si and ³¹P) CPMAS NMR, solution (²⁹Si, ³¹P, ¹H and ¹³C) NMR, and X-ray crystallography. [Note: The moieties of their polyoxoanions are abbreviated simply as 1-3, respectively.] The X-ray molecular structures of EtN-1 and BuN-3 were determined. In EtN-1, two organic groups connected through a siloxane bond (-Si-O-Si- bond) were grafted on a mono-lacunary site of a Keggin POM, whereas in BuN-3 four organic groups connected through siloxane bonds were grafted on a tri-lacunary site of a Keggin POM. In BuN-2, three organic groups were grafted in the form of silanol (-SiOH) on a tri-lacunary site, i.e., in BuN-2 there was no siloxane bond. BuN-3 was synthesized as BuN-3a and BuN-3b by two methods, respectively; (1) BuN-3a was obtained by a 1 : 1 molar-ratio reaction of BuN-2 and an SCA in CH₃CN, and (2) BuN-3b was prepared by a direct 1 : 4 molar-ratio reaction of a tri-lacunary Keggin POM and SCA in water-CH₃CN. X-Ray crystallography revealed that BuN-3a is the same as BuN-3b. It is probable that BuN-2 is an intermediate in the formation of BuN-3. Terminal -SH groups in 1-3, as well as -OH groups in 2, can be utilized for immobilization of POMs and, also, as building blocks for the formation of novel hybrid compounds.

  8. Non-metallic inclusions structure dimension in high quality steel with medium carbon contents

    Directory of Open Access Journals (Sweden)

    T. Lipiński

    2009-07-01

    Full Text Available The experimental material consisted of semi-finished products of high-grade, medium-carbon structural steel. The production process involved two melting technologies: steel melting in a 140-ton basic arc furnace with desulfurization and argon refining variants, and in a 100-ton oxygen converter. Billet samples were collected to analyze the content of non-metallic inclusions with the use of an optical microscope and a video inspection microscope. The results were processed and presented in graphic form.

  9. The Effect of Fine Non-Metallic Inclusions on the Fatigue Strength of Structural Steel

    Directory of Open Access Journals (Sweden)

    Lipiński T.

    2015-04-01

    Full Text Available The article discusses the results of a study investigating the effect of the number of fine non-metallic inclusions (up to 2 µm in size on the fatigue strength of structural steel during rotary bending. The study was performed on 21 heats produced in an industrial plant. Fourteen heats were produced in 140 ton electric furnaces, and 7 heats were performed in a 100 ton oxygen converter. All heats were desulfurized. Seven heats from electrical furnaces were refined with argon, and heats from the converter were subjected to vacuum circulation degassing.

  10. Separation of the metallic and non-metallic fraction from printed circuit boards employing green technology.

    Science.gov (United States)

    Estrada-Ruiz, R H; Flores-Campos, R; Gámez-Altamirano, H A; Velarde-Sánchez, E J

    2016-07-05

    The generation of electrical and electronic waste is increasing day by day; recycling is attractive because of the metallic fraction containing these. Nevertheless, conventional techniques are highly polluting. The comminution of the printed circuit boards followed by an inverse flotation process is a clean technique that allows one to separate the metallic fraction from the non-metallic fraction. It was found that particle size and superficial air velocity are the main variables in the separation of the different fractions. In this way an efficient separation is achieved by avoiding the environmental contamination coupled with the possible utilization of the different fractions obtained. Copyright © 2016 Elsevier B.V. All rights reserved.

  11. A Review of Post and Core Application with Emphasize on Non Metallic Posts

    Directory of Open Access Journals (Sweden)

    Shahroodi MH

    2001-05-01

    Full Text Available Many different methods are suggested to restore endodontically treated teeth. Prefabricated posts can not be indicated for all teeth and cast posts require extra time and cost. In addition, with the introduction of full ceramic restorations, achieving the ideal esthetic with metal post underneath them may be problematic or impossible because the darkness of the metallic posts may show through the highly translucent all ceramic restorations. In this article the review of litature and describiton of applied methods of different procedure in restoring the root canal therapied teeth and few techniques of non metallic posts fabrication such as fiber reinforced composite and zirconium oxide posts have been described.

  12. Charge-transfer induced surface conductivity for a copper based inorganic-organic hybrid

    NARCIS (Netherlands)

    Arkenbout, Anne H.; Uemura, Takafumi; Takeya, Jun; Palstra, Thomas T. M.

    2009-01-01

    Inorganic-organic hybrids are receiving increasing attention as they offer the opportunity to combine the robust properties of inorganic materials with the versatility of organic compounds. We have studied the electric properties of an inorganic-organic hybrid with the chemical formula:

  13. 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

  14. [An optical-fiber-sensor-based spectrophotometer for soil non-metallic nutrient determination].

    Science.gov (United States)

    He, Dong-xian; Hu, Juan-xiu; Lu, Shao-kun; He, Hou-yong

    2012-01-01

    In order to achieve rapid, convenient and efficient soil nutrient determination in soil testing and fertilizer recommendation, a portable optical-fiber-sensor-based spectrophotometer including immersed fiber sensor, flat field holographic concave grating, and diode array detector was developed for soil non-metallic nutrient determination. According to national standard of ultraviolet and visible spectrophotometer with JJG 178-2007, the wavelength accuracy and repeatability, baseline stability, transmittance accuracy and repeatability measured by the prototype instrument were satisfied with the national standard of III level; minimum spectral bandwidth, noise and excursion, and stray light were satisfied with the national standard of IV level. Significant linear relationships with slope of closing to 1 were found between the soil available nutrient contents including soil nitrate nitrogen, ammonia nitrogen, available phosphorus, available sulfur, available boron, and organic matter measured by the prototype instrument compared with that measured by two commercial single-beam-based and dual-beam-based spectrophotometers. No significant differences were revealed from the above comparison data. Therefore, the optical-fiber-sensor-based spectrophotometer can be used for rapid soil non-metallic nutrient determination with a high accuracy.

  15. Solution behavior of hydrogen isotopes and other non-metallic elements in liquid lithium

    Energy Technology Data Exchange (ETDEWEB)

    Maroni, V.A.; Calaway, W.F.; Veleckis, E.; Yonco, R.M.

    1976-01-01

    Results of experimental studies to measure selected thermodynamic properties for systems of lithium with non-metallic elements are reported. Investigations of the Li-H, Li-D, and Li-T systems have led to the elucidation of the dilute solution behavior and the H/D/T isotope effects. In the case of the Li-H and Li-D systems, the principal features of the respective phase diagrams have been delineated. The solubility of Li-D in liquid lithium has been measured down to 200/sup 0/C. The solubility of Li/sub 3/N in liquid lithium and the thermal decomposition of Li/sub 3/N have also been studied. From these data, the free energy of formation of Li/sub 3/N and the Sieverts' constant for dissolution of nitrogen in lithium have been determined. Based on studies of the distribution of non-metallic elements between liquid lithium and selected molten salts, it appears that molten salt extraction offers promise as a means of removing these impurity elements (e.g., H, D, T, O, N, C) from liquid lithium.

  16. Bacterial assimilation reduction of iron in the treatment of non-metallics

    Directory of Open Access Journals (Sweden)

    Peter Malachovský

    2005-11-01

    Full Text Available Natural non-metallics, including granitoide and quartz sands, often contain iron which decreases the whiteness of these raw materials. Insoluble Fe3+ in these samples could be reduced to soluble Fe2+ by bacteria of Bacillus spp. and Saccharomyces spp. The leaching effect, observed by the measurement of Fe2+concentration in a solution, showed higher activities of a bacterial kind isolated from the Bajkal lake and also by using of yeast Saccharomyces sp. during bioleaching of quartz sands. However, allkinds of Bacillus spp. isolated from the Slovak deposit and from Bajkal lake were very active in the iron reduction during bioleaching of the feldspar raw material. This metal was efficiently removed from quartz sands as documented by the Fe2O3 decrease (from 0,317 % to 0,126 % and from feldpars raw materials by the Fe2O3 decrease (from 0,288 % to 0,115 % after bioleaching. The whiteness of these non-metallics was increased during a visual comparison of samples before and after bioleaching but samples contain selected magnetic particles. A removal of iron as well as a release of iron minerals from silicate matrix should increase the effect of the magnetic separation and should give a product which is suitable for industrial applications.

  17. PVC-based composite material containing recycled non-metallic printed circuit board (PCB) powders.

    Science.gov (United States)

    Wang, Xinjie; Guo, Yuwen; Liu, Jingyang; Qiao, Qi; Liang, Jijun

    2010-12-01

    The study is directed to the use of non-metallic powders obtained from comminuted recycled paper-based printed circuit boards (PCBs) as an additive to polyvinyl chloride (PVC) substrate. The physical properties of the non-metallic PCB (NMPCB) powders were measured, and the morphological, mechanical and thermal properties of the NMPCB/PVC composite material were investigated. The results show that recycled NMPCB powders, when added below a threshold, tended to increase the tensile strength and bending strength of PVC. When 20 wt% NMPCB powders (relative to the substrate PVC) of an average diameter of 0.08 mm were added, the composite tensile strength and bending strength reached 22.6 MPa and 39.83 MPa, respectively, representing 107.2% and 123.1% improvement over pure PVC. The elongation at break of the composite material reached 151.94% of that of pure PVC, while the Vicat softening temperature of the composite material did not increase significantly compared to the pure PVC. The above results suggest that paper-based NMPCB powders, when used at appropriate amounts, can be effective for toughening PVC. Thus, this study suggests a new route for reusing paper-based NMPCB, which may have a significant beneficial environmental impact.

  18. A Fully Non-Metallic Gas Turbine Engine Enabled by Additive Manufacturing

    Science.gov (United States)

    Grady, Joseph E.; Halbig, Michael C.; Singh, Mrityunjay

    2015-01-01

    In a NASA Aeronautics Research Institute (NARI) sponsored program entitled "A Fully Non-Metallic Gas Turbine Engine Enabled by Additive Manufacturing", evaluation of emerging materials and additive manufacturing technologies was carried out. These technologies may enable fully non-metallic gas turbine engines in the future. This paper highlights the results of engine system trade studies which were carried out to estimate reduction in engine emissions and fuel burn enabled due to advanced materials and manufacturing processes. A number of key engine components were identified in which advanced materials and additive manufacturing processes would provide the most significant benefits to engine operation. In addition, feasibility of using additive manufacturing technologies to fabricate gas turbine engine components from polymer and ceramic matrix composite were demonstrated. A wide variety of prototype components (inlet guide vanes (IGV), acoustic liners, engine access door) were additively manufactured using high temperature polymer materials. Ceramic matrix composite components included first stage nozzle segments and high pressure turbine nozzle segments for a cooled doublet vane. In addition, IGVs and acoustic liners were tested in simulated engine conditions in test rigs. The test results are reported and discussed in detail.

  19. 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)

  20. 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...

  1. X-ray detection of ingested non-metallic foreign bodies.

    Science.gov (United States)

    Saps, Miguel; Rosen, John M; Ecanow, Jacob

    2014-05-08

    To determine the utility of X-ray in identifying non-metallic foreign body (FB) and assess inter-radiologist agreement in identifying non-metal FB. Focus groups of nurses, fellows, and attending physicians were conducted to determine commonly ingested objects suitable for inclusion. Twelve potentially ingested objects (clay, plastic bead, crayon, plastic ring, plastic army figure, glass bead, paperclip, drywall anchor, eraser, Lego™, plastic triangle toy, and barrette) were embedded in a gelatin slab placed on top of a water-equivalent phantom to simulate density of a child's abdomen. The items were selected due to wide availability and appropriate size for accidental pediatric ingestion. Plain radiography of the embedded FBs was obtained. Five experienced radiologists blinded to number and types of objects were asked to identify the FBs. The radiologist was first asked to count the number of items that were visible then to identify the shape of each item and describe it to a study investigator who recorded all responses. Overall inter-rater reliability was analyzed using percent agreement and κ coefficient. We calculated P value to assess the probability of error involved in accepting the κ value. Fourteen objects were radiographed including 12 original objects and 2 duplicates. The model's validity was supported by clear identification of a radiolucent paperclip as a positive control, and lack of identification of plastic beads (negative control) despite repeated inclusion. Each radiologist identified 7-9 of the 14 objects (mean 8, 67%). Six unique objects (50%) were identified by all radiologists and four unique objects (33%) were not identified by any radiologist (plastic bead, Lego™, plastic triangle toy, and barrette). Identification of objects that were not present, false-positives, occurred 1-2 times per radiologist (mean 1.4). An additional 17% of unique objects were identified by less than half of the radiologists. Agreement between radiologists was

  2. Calculating the Carrying Capacity of Flexural Prestressed Concrete Beams with Non-Metallic Reinforcement

    Directory of Open Access Journals (Sweden)

    Mantas Atutis

    2011-04-01

    Full Text Available The article reviews moment resistance design methods of prestressed concrete beams with fibre-reinforced polymer (FRP reinforcement. FRP tendons exhibit linear elastic response to rupture without yielding and thus failure is expected to be brittle. The structural behaviour of beams prestressed with FRP tendons is different from beams with traditional steel reinforcement. Depending on the reinforcement ratio, the flexural behaviour of the beam can be divided into several groups. The numerical results show that depending on the nature of the element failure, moment resistance calculation results are different by using reviewed methods. It was found, that the use of non-metallic reinforcement in prestressed concrete structures is effective: moment capacity is about 5% higher than that of the beams with conventional steel reinforcement.Article in Lithuanian

  3. The share of non-metallic inclusions in high-grade steel for machine parts

    Directory of Open Access Journals (Sweden)

    T. Lipiński

    2010-10-01

    Full Text Available The aim of this work was to compare the differences in the purity steel in the dimensions of inclusion particles as dependent on various steel production processes. The experimental material consisted of semi-finished products of high-grade, medium-carbon constructional steel with: manganese, chromium, nickel, molybdenum and boron. The impurity content of steel was low as phosphorus and sulphur levels did not exceed 0.025%. The experimental material consisted of steel products obtained in three metallurgical processes: electric, electric with argon refining and oxygen converter with vacuum degassing of steel. Billet samples were collected to determine: chemical composition, relative volume of non-metallic inclusions, dimensions of impurities. The results were processed and presented in graphic form.

  4. Morphology and Orientation Selection of Non-metallic Inclusions in Electrified Molten Metal

    Science.gov (United States)

    Zhao, Z. C.; Qin, R. S.

    2017-10-01

    The effect of electric current on morphology and orientation selection of non-metallic inclusions in molten metal has been investigated using theoretical modeling and numerical calculation. Two geometric factors, namely the circularity ( fc ) and alignment ratio ( fe ) were introduced to describe the inclusions shape and configuration. Electric current free energy was calculated and the values were used to determine the thermodynamic preference between different microstructures. Electric current promotes the development of inclusion along the current direction by either expatiating directional growth or enhancing directional agglomeration. Reconfiguration of the inclusions to reduce the system electric resistance drives the phenomena. The morphology and orientation selection follow the routine to reduce electric free energy. The numerical results are in agreement with our experimental observations.

  5. Nuclide, metal and non metal levels in percolated water from soils fertilized with phosphogypsum

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Camilla Bof; Knupp, Eliana Aparecida Nonato; Palmieri, Helena E.L.; Jacomino, Vanusa Maria Feliciano, E-mail: cgbs@cdtn.b [Nuclear Technology Development Center (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil); Taddei, Maria Helena; Ciqueira, Maria Celia [Pocos de Caldas Lab., (LAPOC/CNEN), Pocos de Caldas, MG (Brazil)

    2009-07-01

    Systematic generation of residues is more and more worrying in today.s world; adequate storage and reutilization are of great importance. Since generation of residues has become impossible to avoid, the possibility of reuse must be studied and researched. An example of these residues is phosphogypsum, which is generated in phosphoric acid production at the rate of around 4.8 tons for each ton of phosphoric acid produced. Many studies seek to reuse phosphogypsum in agriculture as a source of calcium and sulfur, potassium or aluminum, especially in soils from Brazil's cerrado regions. Though phosphogypsum is mainly composed of dehydrated calcium sulfate, it can have high levels of heavy metals, non metals (As and Se), fluorides and natural radionuclides. Thus, its uncontrolled use as a soil conditioner can lead to contamination of underground water. (author)

  6. Analysis and simulation of non-metallic inclusions in spheroidal graphite iron

    Science.gov (United States)

    Pustal, B.; Schelnberger, B.; Bührig-Polaczek, A.

    2016-03-01

    Non-metallic inclusions in spheroidal cast iron (SGI) reduce fatigue strength and yield strength. This type of inclusion usually accumulates at grain boundaries. Papers addressing this topic show the overall impact of both the fraction of so-called white (carbides) and black (non-metallic) inclusions on mechanical properties. In the present work we focus on the origin and the formation conditions of black Mg-bearing inclusions, further distinguishing between Si-bearing and non-Si-bearing Mg inclusions. The formation was simulated applying thermodynamic approaches. Moreover, appropriate experiments have been carried out and a large number of particles have been studied applying innovative feature analysis with regard to shape, size, and composition. Magnesium silicates are predicted at elevated oxygen concentrations, whereas at low levels of oxygen sulphides and carbides appear at a late stage of solidification. Experiments with three consecutive flow obstacles show that the amount of magnesium silicates decrease after each of the three obstacles, whereas the fraction of non-Si-bearing inclusions remains approximately constant. The size of inclusions divides in halves over the flow path and the number of particles increases accordingly. We point out that based on feature analysis Mg-O-C bearing inclusion show disadvantageous form factors for which reason this kind of inclusions may be extremely harmful in terms of crack initiation. All results obtained indicate that magnesium silicates are entrapped on mould filling, whereas Mg-(O, C, S, P, N) bearing particles are precipitates at late stages of solidification. Consequently, the only avoidance strategy is setting up optimum retained magnesium content.

  7. Inorganic UV filters

    Directory of Open Access Journals (Sweden)

    Eloísa Berbel Manaia

    2013-06-01

    Full Text Available Nowadays, concern over skin cancer has been growing more and more, especially in tropical countries where the incidence of UVA/B radiation is higher. The correct use of sunscreen is the most efficient way to prevent the development of this disease. The ingredients of sunscreen can be organic and/or inorganic sun filters. Inorganic filters present some advantages over organic filters, such as photostability, non-irritability and broad spectrum protection. Nevertheless, inorganic filters have a whitening effect in sunscreen formulations owing to the high refractive index, decreasing their esthetic appeal. Many techniques have been developed to overcome this problem and among them, the use of nanotechnology stands out. The estimated amount of nanomaterial in use must increase from 2000 tons in 2004 to a projected 58000 tons in 2020. In this context, this article aims to analyze critically both the different features of the production of inorganic filters (synthesis routes proposed in recent years and the permeability, the safety and other characteristics of the new generation of inorganic filters.

  8. 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.

  9. Influence of non-metallic inclusions on the strength properties of screws made of 35B2+Cr steel after softening

    OpenAIRE

    Krawczyk, J.; Pawłowski, B

    2012-01-01

    Purpose: This paper presents the results of the research on the influence of non-metallic inclusions on strength properties of 35B2+Cr steel screws.Design/methodology/approach: The investigations were carried out on screws after softening. The investigated steels with different fraction of non-metallic inclusions were delivered by three different suppliers.Findings: It was proved, that in spite of the level of fraction of non-metallic inclusions compatible with the corresponding standards, th...

  10. 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.…

  11. Funky inorganic fibers

    NARCIS (Netherlands)

    de Wit, Patrick

    2017-01-01

    Inorganic porous hollow fibers (IPHF) are interesting for various applications that can benefit from a high surface-area-to-volume ratio. Examples include membranes, catalysts, electrodes, and combinations of these. The thesis starts with providing an overview of conceivable materials of which IPHF

  12. 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.

  13. Heterogeneous Catalysis of Polyoxometalate Based Organic-Inorganic Hybrids.

    Science.gov (United States)

    Ren, Yuanhang; Wang, Meiyin; Chen, Xueying; Yue, Bin; He, Heyong

    2015-03-31

    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.

  14. The diesel exhaust in miners study: IV. Estimating historical exposures to diesel exhaust in underground non-metal mining facilities.

    NARCIS (Netherlands)

    Vermeulen, R.; Coble, J.B.; Lubin, J.H.; Portengen, L.; Blair, A.; Attfield, M.D.; Silverman, D.T.; Stewart, P.A.

    2010-01-01

    We developed quantitative estimates of historical exposures to respirable elemental carbon (REC) for an epidemiologic study of mortality, including lung cancer, among diesel-exposed miners at eight non-metal mining facilities [the Diesel Exhaust in Miners Study (DEMS)]. Because there were no histori

  15. Lipophilic super-absorbent polymer gels as surface cleaners for oil and grease from metal and non-metal surfaces

    Science.gov (United States)

    The objective of this research is to develop a new cleaning technology based on lipophilic super-absorbent swelling gels for the removal of oil, grease and particulate matters from metal and non-metal surfaces. It is desired that the cleaner is in solid form and is VOC-exempt, HAP-free, non-toxic, n...

  16. Super-Absorbent polymer gels for oil and grease removal from metal and non-metal surfaces

    Science.gov (United States)

    The objective of this research is to develop a new surface cleaning technology for removal of oil, grease and particulate matters from metal and non-metal surfaces. It is desired that the cleaner is in solid form and is VOC-exempt, HAP-free, non-toxic, non-corrosive, non-ozone depleting, recyclable...

  17. Metals, non-metals and PCB in electrical and electronic waste--actual levels in Switzerland.

    Science.gov (United States)

    Morf, Leo S; Tremp, Josef; Gloor, Rolf; Schuppisser, Felix; Stengele, Markus; Taverna, Ruedi

    2007-01-01

    The chemical composition of waste of small electrical and electronic equipment (s-WEEE), a rapidly growing waste stream, was determined for selected metals (Cu, Sb, Hg etc.) and non-metals (Cl, Br, P) and PCBs. During a 3-day experiment, all output products and the s-WEEE input mass flows in a WEEE recycling plant were measured. Only output products were sampled and analyzed. Material balances were established, applying substance flow analysis (SFA). Transfer coefficients for the selected substances were also determined. The results demonstrate the capability of SFA to determine the composition of the highly heterogeneous WEEE for most substances with rather low uncertainty (2 sigma +/- 30%). The results confirm the growing importance of s-WEEE regarding secondary resource metals and potential toxic substances. Nowadays, the thirty times smaller s-WEEE turns over larger flows for many substances, compared to municipal solid waste. Transfer coefficient results serve to evaluate the separation efficiency of the recycling process and confirm--with the exception of PCB and Hg--the limitation of hand-sorting and mechanical processing to separate pollutants (Cd, Pb, etc.) out of reusable fractions. Regularly applied SFA would serve to assess the efficacy of legislative, organizational and technical measures on the WEEE.

  18. Strength and deformability of concrete beams reinforced by non-metallic fiber and composite rebar

    Science.gov (United States)

    Kudyakov, K. L.; Plevkov, V. S.; Nevskii, A. V.

    2015-01-01

    Production of durable and high-strength concrete structures with unique properties has always been crucial. Therefore special attention has been paid to non-metallic composite and fiber reinforcement. This article describes the experimental research of strength and deformability of concrete beams with dispersed and core fiber-based reinforcement. As composite reinforcement fiberglass reinforced plastic rods with diameters 6 mm and 10 mm are used. Carbon and basalt fibers are used as dispersed reinforcement. The developed experimental program includes designing and production of flexural structures with different parameters of dispersed fiber and composite rebar reinforcement. The preliminary testing of mechanical properties of these materials has shown their effectiveness. Structures underwent bending testing on a special bench by applying flexural static load up to complete destruction. During the tests vertical displacements were recorded, as well as value of actual load, slippage of rebars in concrete, crack formation. As a result of research were obtained structural failure and crack formation graphs, value of fracture load and maximum displacements of the beams at midspan. Analysis of experimental data showed the effectiveness of using dispersed reinforcement of concrete and the need for prestressing of fiberglass composite rebar.

  19. Stepped-Frequency Ground-Penetrating Radar for Detection of Small Non-metallic Buried Objects

    DEFF Research Database (Denmark)

    Jakobsen, Kaj Bjarne; Sørensen, Helge Bjarup Dissing; Nymann, Ole

    1997-01-01

    to an HP8753C Network Analyzer through a 5 m long Sucoflex coaxial cable. The data are collected automatically using an HPIB interface. The collected data contains both the amplitude and phase information of the reflection coefficient. Data are measured at up to a maximum of 401 different frequencies...... at each measurement point using a mesh-grid with a resolution down to 1 mm by 1 mm. The size of the scan area is 1410 mm by 210 mm. Measurements have been performed on loamy soil containing a buried M-56, a non-metallic AP-mine, and various other mine-like objects made of solid plastic, brass, aluminum......, steel, and wood. The presented results are based on probe-data measured at 100 different frequencies at each measurement point and a coarser mesh-grid of 10 mm by 10 mm, since it is found that less probe-data is needed. Our experiments show that even less amount of probe-data may be necessary....

  20. A Fully Non-Metallic Gas Turbine Engine Enabled by Additive Manufacturing

    Science.gov (United States)

    Grady, Joseph E.

    2015-01-01

    The Non-Metallic Gas Turbine Engine project, funded by NASA Aeronautics Research Institute, represents the first comprehensive evaluation of emerging materials and manufacturing technologies that will enable fully nonmetallic gas turbine engines. This will be achieved by assessing the feasibility of using additive manufacturing technologies to fabricate polymer matrix composite and ceramic matrix composite turbine engine components. The benefits include: 50 weight reduction compared to metallic parts, reduced manufacturing costs, reduced part count and rapid design iterations. Two high payoff metallic components have been identified for replacement with PMCs and will be fabricated using fused deposition modeling (FDM) with high temperature polymer filaments. The CMC effort uses a binder jet process to fabricate silicon carbide test coupons and demonstration articles. Microstructural analysis and mechanical testing will be conducted on the PMC and CMC materials. System studies will assess the benefits of fully nonmetallic gas turbine engine in terms of fuel burn, emissions, reduction of part count, and cost. The research project includes a multidisciplinary, multiorganization NASA - industry team that includes experts in ceramic materials and CMCs, polymers and PMCs, structural engineering, additive manufacturing, engine design and analysis, and system analysis.

  1. 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.

  2. Human Exposure and Health Effects of Inorganic and Elemental Mercury

    Science.gov (United States)

    Zheng, Wei

    2012-01-01

    Mercury is a toxic and non-essential metal in the human body. Mercury is ubiquitously distributed in the environment, present in natural products, and exists extensively in items encountered in daily life. There are three forms of mercury, i.e., elemental (or metallic) mercury, inorganic mercury compounds, and organic mercury compounds. This review examines the toxicity of elemental mercury and inorganic mercury compounds. Inorganic mercury compounds are water soluble with a bioavailability of 7% to 15% after ingestion; they are also irritants and cause gastrointestinal symptoms. Upon entering the body, inorganic mercury compounds are accumulated mainly in the kidneys and produce kidney damage. In contrast, human exposure to elemental mercury is mainly by inhalation, followed by rapid absorption and distribution in all major organs. Elemental mercury from ingestion is poorly absorbed with a bioavailability of less than 0.01%. The primary target organs of elemental mercury are the brain and kidney. Elemental mercury is lipid soluble and can cross the blood-brain barrier, while inorganic mercury compounds are not lipid soluble, rendering them unable to cross the blood-brain barrier. Elemental mercury may also enter the brain from the nasal cavity through the olfactory pathway. The blood mercury is a useful biomarker after short-term and high-level exposure, whereas the urine mercury is the ideal biomarker for long-term exposure to both elemental and inorganic mercury, and also as a good indicator of body burden. This review discusses the common sources of mercury exposure, skin lightening products containing mercury and mercury release from dental amalgam filling, two issues that happen in daily life, bear significant public health importance, and yet undergo extensive debate on their safety. PMID:23230464

  3. 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,...

  4. A Fully Non-metallic Gas Turbine Engine Enabled by Additive Manufacturing

    Science.gov (United States)

    Grady, Joseph E.

    2014-01-01

    The Non-Metallic Gas Turbine Engine project, funded by NASA Aeronautics Research Institute (NARI), represents the first comprehensive evaluation of emerging materials and manufacturing technologies that will enable fully nonmetallic gas turbine engines. This will be achieved by assessing the feasibility of using additive manufacturing technologies for fabricating polymer matrix composite (PMC) and ceramic matrix composite (CMC) gas turbine engine components. The benefits of the proposed effort include: 50 weight reduction compared to metallic parts, reduced manufacturing costs due to less machining and no tooling requirements, reduced part count due to net shape single component fabrication, and rapid design change and production iterations. Two high payoff metallic components have been identified for replacement with PMCs and will be fabricated using fused deposition modeling (FDM) with high temperature capable polymer filaments. The first component is an acoustic panel treatment with a honeycomb structure with an integrated back sheet and perforated front sheet. The second component is a compressor inlet guide vane. The CMC effort, which is starting at a lower technology readiness level, will use a binder jet process to fabricate silicon carbide test coupons and demonstration articles. The polymer and ceramic additive manufacturing efforts will advance from monolithic materials toward silicon carbide and carbon fiber reinforced composites for improved properties. Microstructural analysis and mechanical testing will be conducted on the PMC and CMC materials. System studies will assess the benefits of fully nonmetallic gas turbine engine in terms of fuel burn, emissions, reduction of part count, and cost. The proposed effort will be focused on a small 7000 lbf gas turbine engine. However, the concepts are equally applicable to large gas turbine engines. The proposed effort includes a multidisciplinary, multiorganization NASA - industry team that includes experts in

  5. Detection of Non-metallic Inclusions in Centrifugal Continuous Casting Steel Billets

    Science.gov (United States)

    Wang, Qiangqiang; Zhang, Lifeng; Seetharaman, Sridhar; Yang, Shufeng; Yang, Wen; Wang, Yi

    2016-06-01

    In the current study, automated particle analysis was employed to detect non-metallic inclusions in steel during a centrifugal continuous casting process of a high-strength low alloy steel. The morphology, composition, size, area fraction, amount, and spatial distribution of inclusions in steel were obtained. Etching experiment was performed to reveal the dendrite structure of the billet and to discuss the effect of centrifugal force on the distribution of oxide inclusions in the final solidified steel by comparing the solidification velocity with the critical velocity reported in literature. It was found that the amount of inclusions was highest in samples from the tundish (~250 per mm2), followed by samples from the mold (~200 per mm2), and lowest in billet samples (~86 per mm2). In all samples, over 90 pct of the inclusions were smaller than 2μm. In steel billets, the content of oxides, dual-phase oxide-sulfides, and sulfides in inclusions were found to be 10, 30, and 60 pct, respectively. The dual-phase inclusions were oxides with sulfides precipitated on the outer surface. Oxide inclusions consisted of high Al2O3 and high MnO which were solid at the molten steel temperature, implying that the calcium treatment was insufficient. Small oxide inclusions very uniformly distributed on the cross section of the billet, while there were more sulfide inclusions showing a banded structure at the outside 25 mm layer of the billet. The calculated solidification velocity was higher than the upper limit at which inclusions were entrapped by the solidifying front, revealing that for oxide inclusions smaller than 8μm in this study, the centrifugal force had little influence on its final distribution in billets. Instead, oxide inclusions were rapidly entrapped by solidifying front.

  6. Recycling of non-metallic fractions from waste electrical and electronic equipment (WEEE): a review.

    Science.gov (United States)

    Wang, Ruixue; Xu, Zhenming

    2014-08-01

    The world's waste electrical and electronic equipment (WEEE) consumption has increased incredibly in recent decades, which have drawn much attention from the public. However, the major economic driving force for recycling of WEEE is the value of the metallic fractions (MFs). The non-metallic fractions (NMFs), which take up a large proportion of E-wastes, were treated by incineration or landfill in the past. NMFs from WEEE contain heavy metals, brominated flame retardant (BFRs) and other toxic and hazardous substances. Combustion as well as landfill may cause serious environmental problems. Therefore, research on resource reutilization and safe disposal of the NMFs from WEEE has a great significance from the viewpoint of environmental protection. Among the enormous variety of NMFs from WEEE, some of them are quite easy to recycle while others are difficult, such as plastics, glass and NMFs from waste printed circuit boards (WPCBs). In this paper, we mainly focus on the intractable NMFs from WEEE. Methods and technologies of recycling the two types of NMFs from WEEE, plastics, glass are reviewed in this paper. For WEEE plastics, the pyrolysis technology has the lowest energy consumption and the pyrolysis oil could be obtained, but the containing of BFRs makes the pyrolysis recycling process problematic. Supercritical fluids (SCF) and gasification technology have a potentially smaller environmental impact than pyrolysis process, but the energy consumption is higher. With regard to WEEE glass, lead removing is requisite before the reutilization of the cathode ray tube (CRT) funnel glass, and the recycling of liquid crystal display (LCD) glass is economically viable for the containing of precious metals (indium and tin). However, the environmental assessment of the recycling process is essential and important before the industrialized production stage. For example, noise and dust should be evaluated during the glass cutting process. This study could contribute

  7. 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

  8. Numerical analysis of the non-metallic inclusions distribution and separation in a two-strand tundish

    Directory of Open Access Journals (Sweden)

    T. Merder

    2013-04-01

    Full Text Available The tundish plays an important role in the challenging task of a “clean steel” production process. The flow of the liquid steel in tundish has a crucial influence on non-metallic inclusions distribution and separation. The article presents computational studies of non-metallic inclusions separation in a two-strand industrial tundish during steady-state casting. Tundish capacity is 7,5 t. First, flow structure in the tundish was investigated using water model of the industrial tundish in a 1:2 scale. The experimental results, regarding RTD characteristics were used to validate numerical model. With validated model, particle distribution and separation in the two-strand tundish were investigated numerically. For modelling the separation of particles at the fluid surface, a modified boundary condition has been implemented.

  9. An aviation security (AVSEC) screening demonstrator for the detection of non-metallic threats at 28-33 GHz

    Science.gov (United States)

    Salmon, Neil A.; Bowring, Nick; Hutchinson, Simon; Southgate, Matthew; O'Reilly, Dean

    2013-10-01

    The unique selling proposition of millimetre wave technology for security screening is that it provides a stand-off or portal scenario sensing capability for non-metallic threats. The capabilities to detect some non-metallic threats are investigated in this paper, whilst recommissioning the AVSEC portal screening system at the Manchester Metropolitan University. The AVSEC system is a large aperture (1.6 m) portal screening imager which uses spatially incoherent illumination at 28-33 GHz from mode scrambling cavities to illuminate the subject. The imaging capability is critically analysed in terms of this illumination. A novel technique for the measurement of reflectance, refractive index and extinction coefficient is investigated and this then use to characterise the signatures of nitromethane, hexane, methanol, bees wax and baking flour. Millimetre wave images are shown how these liquids in polycarbonate bottles and the other materials appear against the human body.

  10. Tin compounds and insect fauna

    Energy Technology Data Exchange (ETDEWEB)

    Butovskiy, R.O.

    1985-03-01

    A review of the literature of tin compounds serving as pesticides has resulted in the identification of 11 widely used compounds, both organic and inorganic, with largely fungicidal activity. Organotin compounds seem to be limited in use to the control of insect pests, with the majority of the compounds consisting of Sn(IV) and falling into the following four categories: R/sub 4/Sn, R/sub 3/SNX, R/sub 2/SnX/sub 2/, and RSnX/sub 3/, where R = aliphatic or aromatic hydrocarbon radicals, and X = organic or inorganic substituent. The insecticidal activity of these compounds appears to rest on inhibition of ATPase and uncoupling of oxidative phosphorylation. As a result, these compounds act as larvicides, ovicides and imagocides. 77 references.

  11. Cleavage of hydrogen by activation at a single non-metal centre - towards new hydrogen storage materials.

    Science.gov (United States)

    Grabowski, Sławomir J

    2015-05-28

    Molecular surfaces of non-metal species are often characterized by both positive and negative regions of electrostatic potential (EP) at a non-metal centre. This centre may activate molecular hydrogen which further leads to the addition reaction. The positive EP regions at the non-metal centres correspond to σ-holes; the latter sites are enhanced by electronegative substituents. This is why the following simple moieties; PFH2, SFH, AsFH2, SeFH, BrF3, PF(CH3)2 and AsF(CH3)2, were chosen here to analyze the H2 activation and its subsequent splitting at the P, As, S, Se and Br centres. Also the reverse H-H bond reforming process is analyzed. MP2/aug-cc-pVTZ calculations were performed for systems corresponding to different stages of these processes. The sulphur centre in the SFH moiety is analyzed in detail since the potential barrier height for the addition reaction for this species is the lowest of the moieties analyzed here. The results of calculations show that the SFH + H2 → SFH3 reaction in the gas phase is endothermic but it is exothermic in polar solvents.

  12. Synthesis of high molecular weight PEO using non-metal initiators

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Jin; Sivanandan, Kulandaivelu; Pistorino, Jonathan; Eitouni, Hany Basam

    2015-05-19

    A new synthetic method to prepare high molecular weight poly(ethylene oxide) with a very narrow molecular weight distribution (PDI<1.5) is described. The method involves a metal free initiator system, thus avoiding dangerous, flammable organometallic compounds.

  13. Recycling of non-metallic fractions from waste electrical and electronic equipment (WEEE): A review

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Ruixue; Xu, Zhenming, E-mail: zmxu@sjtu.edu.cn

    2014-08-15

    Highlights: • NMFs from WEEE were treated by incineration or land filling in the past. • Environmental risks such as heavy metals and BFRs will be the major problems during the NMFs recycling processes. • Methods and technologies of recycling the two types of NMFs from WEEE, plastics, glasses are reviewed. • More environmental impact assessment should be carried out to evaluate the environmental risks of the recycling products. - Abstract: The world’s waste electrical and electronic equipment (WEEE) consumption has increased incredibly in recent decades, which have drawn much attention from the public. However, the major economic driving force for recycling of WEEE is the value of the metallic fractions (MFs). The non-metallic fractions (NMFs), which take up a large proportion of E-wastes, were treated by incineration or landfill in the past. NMFs from WEEE contain heavy metals, brominated flame retardant (BFRs) and other toxic and hazardous substances. Combustion as well as landfill may cause serious environmental problems. Therefore, research on resource reutilization and safe disposal of the NMFs from WEEE has a great significance from the viewpoint of environmental protection. Among the enormous variety of NMFs from WEEE, some of them are quite easy to recycle while others are difficult, such as plastics, glass and NMFs from waste printed circuit boards (WPCBs). In this paper, we mainly focus on the intractable NMFs from WEEE. Methods and technologies of recycling the two types of NMFs from WEEE, plastics, glass are reviewed in this paper. For WEEE plastics, the pyrolysis technology has the lowest energy consumption and the pyrolysis oil could be obtained, but the containing of BFRs makes the pyrolysis recycling process problematic. Supercritical fluids (SCF) and gasification technology have a potentially smaller environmental impact than pyrolysis process, but the energy consumption is higher. With regard to WEEE glass, lead removing is requisite

  14. Filmogen organic-inorganic hybrids obtained by sol-gel in the presence of cationic polymer

    NARCIS (Netherlands)

    Donescu, Dan; Serban, Sever; Uricanu, Violeta; Duits, Michel; Perichaud, Alain; Olteanu, Mihaela; Spiroiu, Manuela; Vasilescu, Marilena

    2007-01-01

    Self-standing and coated-on-glass films were prepared from polymer-inorganic ormosils, using the cationic polymer poly(methacrylamide propyl quaternarydimethyldodecyl bromide). The inorganic compound was grown in sol-gel reactions based on methyltriethoxysilane (MeTES), with or without addition of t

  15. (EDT-TTF-CONH2)6[Re6Se8(CN)6], a metallic Kagome-type organic-inorganic hybrid compound: electronic instability, molecular motion, and charge localization.

    Science.gov (United States)

    Baudron, Stéphane A; Batail, Patrick; Coulon, Claude; Clérac, Rodolphe; Canadell, Enric; Laukhin, Vladimir; Melzi, Roberto; Wzietek, Pawel; Jérome, Denis; Auban-Senzier, Pascale; Ravy, Sylvain

    2005-08-24

    (EDT-TTF-CONH2)6[Re6Se8(CN)6], space group R, was prepared by electrocrystallization from the primary amide-functionalized ethylenedithiotetrathiafulvalene, EDT-TTF-CONH2 (E(1/2)1 = 0.49 V vs SCE in CH3CN), and the molecular cluster tetraanion, [Re6Se8(CN)6]4- (E(1/2) = 0.33 V vs SCE in CH3CN), equipped with hydrogen bond donor and hydrogen bond acceptor functionalities, respectively. Its Kagome topology is unprecedented for any TTF-based materials. The metallic state observed at room temperature has a strong two-dimensional character, in coherence with the Kagome lattice symmetry, and the presence of minute amounts of [Re6Se8(CN)6](3-)* identified by electron spin spectroscopy. A structural instability toward a distorted form of the Kagome topology of lesser symmetry is observed at ca. 180 K. The low-temperature structure is associated with a localized, electrically insulating electronic ground state and its magnetic susceptibility accounted for by a model of uniform chains of localized S = 1/2 spins in agreement with the 100 K triclinic crystal structure and band structure calculations. A sliding motion, within one out of the three (EDT-TTF-CONH2)2 dimers coupled to the [Re6Se8(CN6)(3-)*]/[Re6Se8(CN6)4-] proportion at any temperature, and the electronic ground state of the organic-inorganic hybrid material are analyzed on the basis of ESR, dc conductivity, 1H spin-lattice relaxation, and static susceptibility data which qualify a Mott localization in [EDT-TTF-CONH2]6[Re6Se8(CN)6]. The coupling between the metal-insulator transition and a structural transition allows for the lifting of a degeneracy due to the ternary axis in the high temperature, strongly correlated metallic phase which, in turn, leads to Heisenberg chains at low temperature.

  16. 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.

  17. Tunable Dielectric Responses Triggered by Dimensionality Modification in Organic-Inorganic Hybrid Phase Transition Compounds (C5H6N)CdnCl2n+1 (n = 1 and 2).

    Science.gov (United States)

    Sun, Xiao-Fen; Wang, Zhongxia; Li, Peng-Fei; Liao, Wei-Qiang; Ye, Heng-Yun; Zhang, Yi

    2017-03-20

    Two hybrids (C5H6N)CdCl3 (1) and (C5H6N)Cd2Cl5 (2) were synthesized by stoichiometric regulation of reactants. 1 with a one-dimensional chain-like structure shows a step-like dielectric anomaly at around 158 K. 2 with a layered structure undergoes a prominent phase transition in the vicinity of 182 K, accompanying obvious dielectric relaxation behavior in a broad temperature range. Systematic characterization, such as differential scanning calorimetry (DSC), single-crystal X-ray diffraction, and dielectric measurements, has demonstrated that the phase transitions of 1 and 2 are both attributable to the dynamic motion of the organic cation. Significantly, dimensionality modulation triggers the tunable dielectric responses in these two compounds. Thus, regulation of the phase transition temperature and dielectric responses in the various dimensions of the structure is a potentially effective method to construct tunable dielectric phase transition materials.

  18. NATURE AND CHARACTER OF NON-METALLIC IMPURITIES IN HIGH-MANGANESE STEEL

    Directory of Open Access Journals (Sweden)

    A. I. Garost

    2006-01-01

    Full Text Available The nature of поп-metallic impurities of high-manganese wear-resistant steel is investigated by means of scanning electronic microscopy. The optimal compounds of complex additives (titan, vanadium, chromium, molybdenum, nitrogen, providing the highest operational characteristics of details, are determined.

  19. Computer-Assisted Inverse Design of Inorganic Electrides

    Directory of Open Access Journals (Sweden)

    Yunwei Zhang

    2017-02-01

    Full Text Available 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.

  20. 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.

  1. Numerical 2D and 3D Investigation of Non-Metallic (Glass, Carbon) Fiber Pull-Out Micromechanics 9in Concrete Matrix)

    OpenAIRE

    Khabaz, A; Krasņikovs, A; Kononova, O; Mačanovskis, A

    2010-01-01

    Short non-metallic (glass, carbon) fibre use for concrete disperse reinforcment is of particular interest, because of much higher fibre/matrix interface area value comparing to industrially produced steel fibres.

  2. Experimental and numerical investigation of concrete structures with metal and non-metal reinforcement at impulse loadings

    Science.gov (United States)

    Radchenko, P. A.; Batuev, S. P.; Radchenko, A. V.; Plevkov, V. S.; Kudyakov, K. L.

    2016-11-01

    Manufacturing durable and high-strength concrete structures has always been a relevant objective. Therefore special attention has been paid to non-metallic composite reinforcement. This paper considers experimental and numerical studies of nature of fracture and crack formation in concrete beams with rod composite reinforcement. Fiber glass rods, 6 mm in diameter, have been used as composite reinforcement. Concrete elements have been tested under dynamic load using special pile driver. The obtained results include patterns of fracture and crack formation, maximum load value and maximum element deflection. Comparative analysis of numerical and experimental studies has been held.

  3. Influence of Low-Alloy Cast Steel Modification on Primary Structure Refinement, Type and Shape of Non-Metallic Inclusions

    Directory of Open Access Journals (Sweden)

    Bartocha D.

    2015-04-01

    Full Text Available In the article there are presented methods and results of investigation which main aim were determination of influence of melting technology (gas extraction, vacuum refining, slag refining and extraction, deoxidation and degassing and type of used modifiers on the type and shape of non-metallic inclusions and the primary structure refining. Low alloy cast steel melted in laboratory conditions, in an inductive furnace was investigated. Additions of FeNb, FeV, FeTi and FeZr modifiers were applied. The contents of oxygen and nitrogen in obtained cast steel were determined.

  4. 非金属矿物在医药行业的应用与前景%Medicinal Application and Prospect of Non-metallic Mineral

    Institute of Scientific and Technical Information of China (English)

    鲍康德; 周春晖

    2012-01-01

    Deep procession of non-metallic mineral and application on bio-/medicinal area is a new high-technical industry. This paper summarizes the appl ication history and status in quo of non-metallic minerals in pharmaceutical industry; identification, classification and development tendency of non-metallic minerals for pharmaceutical use. The focus is to introduce the development history of non-metallic minerals for pharmaceutical use, and explore the application prospect of non-metallic minerals in pharmaceutical industry, so as to provide theory basis for sufficiently exploring the potential of non-metallic minerals.%非金属矿物深加工并被用于生物医药领域系高新技术产业.本文综述了非金属矿物的医药应用历史、现状;药用非金属矿物的鉴别、分类和发展趋势.重点介绍了非金属矿物的药用开发历程,并展望了非金属矿物在医药行业的应用前景,以期为充分发掘非金属矿物的潜能提供理论指导.

  5. Synthesis, X-ray crystal structure and highly non-linear optical properties of inorganic-organic hybrid compound: 1,4-Diazbicyclo-octane oxonium tri- nitrates single crystal

    Science.gov (United States)

    Henchiri, Rokaya; Ennaceur, Nasreddine; Cordier, Marie; Ledoux-Rak, Isabelle; Elaloui, Elimame

    2017-07-01

    A new nonlinear optical hybrid crystal 1,4-Diazbicyclo[222]octane oxonium tri-nitrates (DOTN), of the dimension 4×12×1 mm3. The crystal was grown using water as solvent at room temperature and crystal structure was determined by X-Ray diffraction respectively, this title compound was shown to crystallize in non-centrosymmetric trigonal system with space group P31c. The recorded FTIR spectrum has proven the presence of various functional groups in the grown crystal as well as the formation of DOTN. Besides, the thermal stability and melting temperature of the DOTN crystal were identified from the TG/DSC analysis. The suitability of this material for optical application was studied by non-linear optical (NLO) and UV-visible absorption techniques. Furthermore, the nonlinear optical property was analyzed by Kurtz-Perry powder technique and was 3.4 times than that of KDP (potassium dihydrogen phosphate) single crystals. The first hyperpolarizability of nitrate was determined by Second Harmonic light Scattering.

  6. Reduction of ethylenediaminetetraacetic acid iron(III) by Klebsiella sp. FD-3 immobilized on iron(II, III) oxide poly (styrene-glycidyl methacrylate) magnetic porous microspheres: effects of inorganic compounds and kinetic study of effective diffusion in porous media.

    Science.gov (United States)

    Zhou, Zuo-Ming; Wang, Xiao-Yan; Lin, Tian-Ming; Jing, Guo-Hua

    2014-11-01

    Fe3O4 poly (styrene-glycidyl methacrylate) magnetic porous microspheres (MPPMs) were introduced to immobilize Klebsiella sp. FD-3, an iron-reducing bacterium applied to reduce Fe(III)EDTA. The effects of potential inhibitors (S(2-), SO3(2-), NO3(-), NO2(-) and Fe(II)EDTA-NO) on Fe(III)EDTA reduction were investigated. S(2-) reacted with Fe(III)EDTA as an electron-shuttling compound and enhanced the reduction. But Fe(III)EDTA reduction was inhibited by SO3(2-) and Fe(II)EDTA-NO due to their toxic to microorganisms. Low concentrations of NO3(-) and NO2(-) accelerated Fe(III)EDTA reduction, but high concentrations inhibited the reduction, whether by free or immobilized FD-3. The immobilized FD-3 performed better than freely-suspended style. The substrate mass transfer and diffusion kinetics in the porous microspheres were calculated. The value of Thiele modulus and effectiveness factors showed that the intraparticle diffusion was fairly small and neglected in this carrier. Fe(III)EDTA reduction fitted first-order model at low Fe(III)EDTA concentration, and changed to zero-order model at high concentrations. Copyright © 2014 Elsevier Ltd. All rights reserved.

  7. 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.

  8. 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.

  9. Scintillation properties of (C sub 6 H sub 1 sub 3 NH sub 3) sub 2 PbI sub 4 Exciton luminescence of an organic/inorganic multiple quantum well structure compound induced by 2.0 MeV protons

    CERN Document Server

    Shibuya, K; Takeoka, Y; Asai, K

    2002-01-01

    We report a new type of scintillator especially suitable for pulse-radiation detection. Thin films of organic/inorganic perovskite compound (n-C sub 6 H sub 1 sub 3 NH sub 3) sub 2 PbI sub 4 , which is characterized by a multiple quantum well structure, were bombarded by 2.0 MeV protons, and their radiation-induced emission spectra were obtained. A single and sharp emission peak due to an exciton was observed at the wavelength of 524 nm. This emission was clearly detected even at room temperature, and its quantum efficiency was very high. The line shape of this emission did not change, retaining its sharpness, and no other emissions appeared throughout the irradiation. The optical response of (n-C sub 6 H sub 1 sub 3 NH sub 3) sub 2 PbI sub 4 is very fast. (n-C sub 6 H sub 1 sub 3 NH sub 3) sub 2 PbI sub 4 is a promising scintillator material, meeting requirements not satisfied by conventional scintillators.

  10. Study on Non-Metallic Inclusions in Laser-Welded TRIP-Aided Nb-Microalloyed Steel

    Directory of Open Access Journals (Sweden)

    Grajcar A.

    2014-10-01

    Full Text Available The work concerns the studies on non-metallic inclusions occuring in laser-welded Si-Al TRIP steel containing Nb and Ti microadditions. Laser welding tests of 2 mm thick thermomechanically rolled sheets were carried out using keyhole welding and a solid-state laser. The results of laser welding in the air atmosphere for the heat input value of 0.048 kJ/mm are included. The distribution, type and chemical composition of non-metallic inclusions formed in the base metal, heat-affected zone, and fusion zone are analysed in detail. It was found that the base metal contains rare, fine oxysulphides. Their chemical composition was modified by rare earth elements. Numerous oxide inclusions of a various size and a chemical composition occur in the fusion zone. The dependence between a size of particles and their chemical composition was observed. A microstructure of steel was assessed using light microscopy and scanning electron microscopy techniques.

  11. Non-Metallic Inclusions and Hot-Working Behaviour of Advanced High-Strength Medium-Mn Steels

    Directory of Open Access Journals (Sweden)

    Grajcar A.

    2016-06-01

    Full Text Available The work addresses the production of medium-Mn steels with an increased Al content. The special attention is focused on the identification of non-metallic inclusions and their modification using rare earth elements. The conditions of the thermomechanical treatment using the metallurgical Gleeble simulator and the semi-industrial hot rolling line were designed for steels containing 3 and 5% Mn. Hot-working conditions and controlled cooling strategies with the isothermal holding of steel at 400°C were selected. The effect of Mn content on the hot-working behaviour and microstructure of steel was addressed. The force-energetic parameters of hot rolling were determined. The identification of structural constituents was performed using light microscopy and scanning electron microscopy methods. The addition of rare earth elements led to the total modification of non-metallic inclusions, i.e., they replaced Mn and Al forming complex oxysulphides. The Mn content in a range between 3 and 5% does not affect the inclusion type and the hot-working behaviour. In contrast, it was found that Mn has a significant effect on a microstructure.

  12. AES and SIMS analysis of non-metallic inclusions in a low-carbon chromium-steel.

    Science.gov (United States)

    Gammer, Katharina; Rosner, M; Poeckl, G; Hutter, H

    2003-05-01

    In the final step of secondary metallurgical steel processing, calcium is added. Besides Mg, Ca is the most powerful deoxidiser and desulfurisation agent. It reacts with dissolved oxygen and sulfur and reduces oxides and sulfides thereby forming non-metallic inclusions. Within this paper we present the analysis of such inclusions in a low-carbon chromium-steel. Depending on the time of quenching of the steel sample, different structures were revealed by REM, Auger and SIMS: If the steel was quenched immediately after Ca-addition, non-metallic inclusions that appeared to have "cavities" could be detected with SEM. SIMS investigations of these particles showed ring-shaped structures and revealed that the ring is made up of Al, Ca, Mg, O and S. No secondary ions however could be retrieved from the core inside the ring, thus leaving the nature of the "cavities" unclear. If the steel sample was quenched 3 min after Ca addition, inclusions did not have a ring-shaped structure but a compact one.

  13. 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

  14. 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.

  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. Non-metal doped TiO2 nanotube arrays for high efficiency photocatalytic decomposition of organic species in water

    Science.gov (United States)

    Szkoda, Mariusz; Siuzdak, Katarzyna; Lisowska-Oleksiak, Anna

    2016-10-01

    Titanium dioxide is a well-known photoactive semiconductor with a variety of possible applications. The procedure of pollutant degradation is mainly performed using TiO2 powder suspension. It can also be exploited an immobilized catalyst on a solid support. Morphology and chemical doping have a great influence on TiO2 activity under illumination. Here we compare photoactivity of titania nanotube arrays doped with non-metal atoms: nitrogen, iodine and boron applied for photodegradation of organic dye - methylene blue and terephtalic acid. The doped samples act as a much better photocatalyst in the degradation process of methylene blue and lead to the formation of much higher amount of hydroxyl radicals (•OH) than undoped TiO2 nanotube arrays. The use of a catalyst active under solar light illumination in the form of thin films on a stable substrate can be scaled up for an industrial application.

  17. Effect of Non-metallic Inclusions in Fe-Al-Ti-O-N-S Alloy on Grain Size

    Science.gov (United States)

    Choi, Wonjin; Matsuura, Hiroyuki; Tsukihashi, Fumitaka

    2016-06-01

    The effect of characteristics of non-metallic inclusions in Fe-Al-Ti-O-N-S alloys with various compositions at 1473 K (1200 °C) on the microstructure was studied. The ASTM grain size number was determined in as-cast and heated samples by the optical microscopy, and the inclusion types in each sample were determined from composition analysis by field-emission scanning electron microscope with energy-dispersive spectroscopy. The TiN-based inclusions certainly had a positive effect on the grain refinement. On the other hand, TiS-based inclusions exhibited no influence on the decrease of grain size. In addition, the formation and evolution behavior of inclusions by heating solid-state Fe-Al-Ti-O-N-S alloys with those locations were clarified. A different change of inclusions in alloys was observed depending on the distribution and composition of inclusions.

  18. Characteristics and Modification of Non-metallic Inclusions in Titanium-Stabilized AISI 409 Ferritic Stainless Steel

    Science.gov (United States)

    Kruger, Dirk; Garbers-Craig, Andrie

    2017-06-01

    This study describes an investigation into the improvement of castability, final surface quality and formability of titanium-stabilized AISI 409 ferritic stainless steel on an industrial scale. Non-metallic inclusions found in this industrially produced stainless steel were first characterized using SEM-EDS analyses through the INCA-Steel software platform. Inclusions were found to consist of a MgO·Al2O3 spinel core, which acted as heterogeneous nucleation site for titanium solubility products. Plant-scale experiments were conducted to either prevent the formation of spinel, or to modify it by calcium treatment. Modification to spherical dual-phase spinel-liquid matrix inclusions was achieved with calcium addition, which eliminated submerged entry nozzle clogging for this grade. Complete modification to homogeneous liquid calcium aluminates was achieved at high levels of dissolved aluminum. A mechanism was suggested to explain the extent of modification achieved.

  19. Detection of Surface and Subsurface Cracks in Metallic and Non-Metallic Materials Using a Complementary Split-Ring Resonator

    Directory of Open Access Journals (Sweden)

    Ali Albishi

    2014-10-01

    Full Text Available Available microwave techniques for crack detection have some challenges, such as design complexity and working at a high frequency. These challenges make the sensing apparatus design complex and relatively very expensive. This paper presents a simple method for surface and subsurface crack detection in metallic and non-metallic materials based on complementary split-ring resonators (CSRRs. A CSRR sensor can be patterned on the ground plane of a microstrip line and fabricated using printed circuit board technology. Compared to available microwave techniques for sub-millimeter crack detection, the methods presented here show distinct advantages, such as high spatial resolution, high sensitivity and design simplicity. The response of the CSRR as a sensor for crack detection is studied and analysed numerically. Experimental validations are also presented.

  20. Characteristics and Modification of Non-metallic Inclusions in Titanium-Stabilized AISI 409 Ferritic Stainless Steel

    Science.gov (United States)

    Kruger, Dirk; Garbers-Craig, Andrie

    2017-02-01

    This study describes an investigation into the improvement of castability, final surface quality and formability of titanium-stabilized AISI 409 ferritic stainless steel on an industrial scale. Non-metallic inclusions found in this industrially produced stainless steel were first characterized using SEM-EDS analyses through the INCA-Steel software platform. Inclusions were found to consist of a MgO·Al2O3 spinel core, which acted as heterogeneous nucleation site for titanium solubility products. Plant-scale experiments were conducted to either prevent the formation of spinel, or to modify it by calcium treatment. Modification to spherical dual-phase spinel-liquid matrix inclusions was achieved with calcium addition, which eliminated submerged entry nozzle clogging for this grade. Complete modification to homogeneous liquid calcium aluminates was achieved at high levels of dissolved aluminum. A mechanism was suggested to explain the extent of modification achieved.

  1. Standard practice for process compensated resonance testing via swept sine input for metallic and Non-Metallic parts

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2010-01-01

    1.1 This practice describes a general procedure for using the process compensated resonance testing (PCRT) via swept sine input method to identify metallic and non-metallic parts’ resonant pattern differences that can be used to indentify parts with anomalies causing deficiencies in the expected performance of the part in service. This practice is intended for use with instruments capable of exciting, measuring, recording, and analyzing multiple whole body mechanical vibration resonant frequencies within parts exhibiting acoustical ringing in the audio, or ultrasonic, resonant frequency ranges, or both. PCRT is used in the presence of manufacturing process variance to distinguish acceptable parts from those containing significant anomalies in physical characteristics expected to significantly alter the performance. Such physical characteristics include, but are not limited to, cracks, voids, porosity, shrink, inclusions, discontinuities, grain and crystalline structure differences, density related anomalies...

  2. The uncertainties calculation of acoustic method for measurement of dissipative properties of heterogeneous non-metallic materials

    Directory of Open Access Journals (Sweden)

    Мaryna O. Golofeyeva

    2015-12-01

    Full Text Available The effective use of heterogeneous non-metallic materials and structures needs measurement of reliable values of dissipation characteristics, as well as common factors of their change during the loading process. Aim: The aim of this study is to prepare the budget for measurement uncertainty of dissipative properties of composite materials. Materials and Methods: The method used to study the vibrational energy dissipation characteristics based on coupling of vibrations damping decrement and acoustic velocity in a non-metallic heterogeneous material is reviewed. The proposed method allows finding the dependence of damping on vibrations amplitude and frequency of strain-stress state of material. Results: Research of the accuracy of measurement method during the definition of decrement attenuation of fluctuations in synthegran was performed. The international approach for evaluation of measurements quality is used. It includes the common practice international rules for uncertainty expression and their summation. These rules are used as internationally acknowledged confidence measure to the measurement results, which includes testing. The uncertainties budgeting of acoustic method for measurement of dissipative properties of materials were compiled. Conclusions: It was defined that there are two groups of reasons resulting in errors during measurement of materials dissipative properties. The first group of errors contains of parameters changing of calibrated bump in tolerance limits, displacement of sensor in repeated placement to measurement point, layer thickness variation of contact agent because of irregular hold-down of resolvers to control surface, inaccuracy in reading and etc. The second group of errors is linked with density and Poisson’s ratio measurement errors, distance between sensors, time difference between signals of vibroacoustic sensors.

  3. Effect of Acid-Soluble Aluminum on the Evolution of Non-metallic Inclusions in Spring Steel

    Science.gov (United States)

    Wang, Yong; Tang, Haiyan; Wu, Tuo; Wu, Guanghui; Li, Jingshe

    2017-04-01

    The content of acidic soluble aluminum in molten steel ([Al]s) is of significance to the control of total oxygen (TO), the formation of non-metallic inclusions, and the improvement of the surface quality of billets. Industrial trials and thermodynamic calculations were performed to study the effects of [Al]s content on the TO and the evolution of non-metallic inclusions in 60Si2Mn-Cr spring steel that was deoxidized by Si-Mn ((low aluminum process (LAP)) and Si-Mn-Al (high aluminum process (HAP)). The results show that the [Al]s contents in billets are within 0.0060 to 0.0069 mass pct in the LAP and 0.016 to 0.055 mass pct in the HAP. The TO content at each station of the LAP is higher than that in the HAP; the inclusions of billets were mainly of the CaO-Al2O3-SiO2 type in the former, and of the CaO-Al2O3-MgO and CaS-Al2O3-MgO types in the latter. A tendency is found that the higher the [Al]s, the easier it is to deviate from the low melting point region of the inclusion distribution and the larger the size of the inclusions. The relationships between [Al]s and the melting point of the oxide inclusions and the Al2O3 content in the oxide inclusions are also discussed in terms of experiment and calculation.

  4. Enhanced hydrogen desorption properties of magnesium hydride by coupling non-metal doping and nano-confinement

    Science.gov (United States)

    He, Daliang; Wang, Yulong; Wu, Chengzhang; Li, Qian; Ding, Weizhong; Sun, Chenghua

    2015-12-01

    Magnesium hydride (MgH2) offers excellent capacity to store hydrogen, but it suffers from the high desorption temperature (>283 °C for starting release hydrogen). In this work, we calculated the hydrogen desorption energy of Mg76H152 clusters with/without non-metal dopants by density functional theory method. Phosphorus (P), as identified as the best dopant, can reduce the reaction energy for releasing one hydrogen molecule from 0.75 eV (bulk MgH2) to 0.20 eV. Inspired by the calculation, P-doped ordered mesoporous carbon (CMK-3) was synthesized by one-step method and employed as the scaffold for loading MgH2 nanoparticles, forming MgH2@P/CMK-3. Element analysis shows that phosphorus dopants have been incorporated into the CMK-3 scaffold and magnesium and phosphorus elements are well-distributed in carbon scaffold hosts. Tests of hydrogen desorption confirmed that P-doping can remarkably enhance the hydrogen release properties of nanoconfined MgH2 at low temperature, specifically ˜1.5 wt. % H2 released from MgH2@P/CMK-3 below 200 °C. This work, based on the combination of computational calculations and experimental studies, demonstrated that the combined approach of non-metal doping and nano-confinement is promising for enhancing the hydrogen desorption properties of MgH2, which provides a strategy to address the challenge of hydrogen desorption from MgH2 at mild operational conditions.

  5. Miniaturized preconcentration methods based on liquid-liquid extraction and their application in inorganic ultratrace analysis and speciation: A review

    Science.gov (United States)

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

    2009-01-01

    Liquid-liquid extraction (LLE) is widely used as a pre-treatment technique for separation and preconcentration of both organic and inorganic analytes from aqueous samples. Nevertheless, it has several drawbacks, such as emulsion formation or the use of large volumes of solvents, which makes LLE expensive and labour intensive. Therefore, miniaturization of conventional liquid-liquid extraction is needed. The search for alternatives to the conventional LLE using negligible volumes of extractant and the minimum number of steps has driven the development of three new miniaturized methodologies, i.e. single-drop microextraction (SDME), hollow fibre liquid-phase microextraction (HF-LPME) and dispersive liquid-liquid microextraction (DLLME). The aim of this paper is to provide an overview of these novel preconcentration approaches and their potential use in analytical labs involved in inorganic (ultra)trace analysis and speciation. Relevant applications to the determination of metal ions, metalloids, organometals and non-metals are included.

  6. Miniaturized preconcentration methods based on liquid-liquid extraction and their application in inorganic ultratrace analysis and speciation: A review

    Energy Technology Data Exchange (ETDEWEB)

    Pena-Pereira, Francisco; Lavilla, Isela [Departamento de Quimica Analitica y Alimentaria, Area de Quimica Analitica, Facultad de Quimica, Universidad de Vigo, Campus As Lagoas-Marcosende s/n, 36310 Vigo (Spain); Bendicho, Carlos [Departamento de Quimica Analitica y Alimentaria, Area de Quimica Analitica, Facultad de Quimica, Universidad de Vigo, Campus As Lagoas-Marcosende s/n, 36310 Vigo (Spain)], E-mail: bendicho@uvigo.es

    2009-01-15

    Liquid-liquid extraction (LLE) is widely used as a pre-treatment technique for separation and preconcentration of both organic and inorganic analytes from aqueous samples. Nevertheless, it has several drawbacks, such as emulsion formation or the use of large volumes of solvents, which makes LLE expensive and labour intensive. Therefore, miniaturization of conventional liquid-liquid extraction is needed. The search for alternatives to the conventional LLE using negligible volumes of extractant and the minimum number of steps has driven the development of three new miniaturized methodologies, i.e. single-drop microextraction (SDME), hollow fibre liquid-phase microextraction (HF-LPME) and dispersive liquid-liquid microextraction (DLLME). The aim of this paper is to provide an overview of these novel preconcentration approaches and their potential use in analytical labs involved in inorganic (ultra)trace analysis and speciation. Relevant applications to the determination of metal ions, metalloids, organometals and non-metals are included.

  7. 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...

  8. 有机无机专用复合肥对葡萄产量、品质和养分利用的影响%Effects of organic-inorganic special compound fertilizer on yield, quality and nutrient uptake of grape (Vitis labrus-cana Kyoho)

    Institute of Scientific and Technical Information of China (English)

    周媛; 谭启玲; 胡承孝; 郑苍松; 李路; 刘清荣; 胥剑雯

    2015-01-01

    Field experiment was conducted to study the effects of organic-inorganic special compound fertilizer ( OISCF) on fruit yield, quality, and nutrient uptake of grape. Four treatments were set:CK ( no fertilizer) , XG ( traditional fertiliza-tion) , DL ( equal total of N, P2 O5 , K2 O amount of OISCF was used instead of normal fertilizers) and TJ ( recommend a-mount of OISCF) . The results showed that the grape yield of TJ was increased by 25. 8% and 5. 1% comparing with CK and XG respectively. Compared to CK, XG and DL treatments, the TJ grape fruits titratable acid decreased significantly by 10. 7% ~42. 9%, total soluble solid increased by 1. 8% ~8. 2%, Vitamin C increased by 6. 4% ~77. 7%, and TA/TSS increased by 10. 2% ~60. 4%. However, the total amount of N, P2 O5 and K2 O fertilization of TJ treatment was 42. 5%less than the treatments of XG and DL, while grape leaf Fe, Cu contents and fruit Fe absorption were increased significantly by organic-inorganic special compound fertilizer. In conclusion, recommended fertilization of OISCF kept grape fruit yield and improved fruit quality but declined the N, P2 O5 and K2 O application rate considerably.%通过田间小区试验,研究了有机无机专用复合肥对葡萄产量、品质、养分吸收及累积量的影响。结果表明:施用推荐量专用肥,葡萄产量比不施肥和习惯施肥分别增加了25.8%和5.1%;葡萄果实可滴定酸比不施肥、习惯施肥和等量专用肥显著降低,减幅为10.7%~42.9%;施用推荐量专用肥提高了葡萄果实可溶性固形物1.8%~8.2%、 Vc 6.4%~77.7%以及固酸比10.2%~60.4%;施用专用肥显著提高葡萄叶片Fe、 Cu及果实Fe含量;而施用推荐量专用肥比习惯施肥、等量专用肥处理减少氮磷钾施用总量42.5%。因此,施用推荐量有机无机专用复合肥,既保证葡萄产量、改善果实品质,又减少氮磷钾施用总量,节约成本。

  9. Chlorobenzene outputs from combustion of chlorinated organic and inorganic compounds

    Energy Technology Data Exchange (ETDEWEB)

    Green, A.E.S.; Vitali, J.A.; Miller, T.L. [Univ. of Florida, Gainesville, FL (United States)

    1994-12-31

    The authors consider the gas phase formation of chlorinated benzenes and phenols as precursors of chlorinated dioxins and furans from the combustion of solid fuels containing organically bound chlorine. The model investigated is intended to apply to the combustion of medical waste, municipal waste and coals containing chlorine. Assuming a temperature-time profile drawn from incinerator experiments, the authors use kinetic modeling with known reaction rates to further investigate four models of chlorinated benzene formation. Since reaction rates for most chlorination processes are now known, the authors choose simple systems of reaction rates that yield outputs that can be made approximately compatible with results of the Pittsfield-Vicon incinerator and Clean Combustion Technology Laboratory experiments. The authors also consider recent measurements of HCI emissions from crematoria and the implication of this work with respect to the benefits of material substitution in medical and municipal waste incineration. These benefits should also accompany the dechlorination of coals. The authors note the disparity between the prevailing USA position and the emerging position of Germany on the issue of halogenated plastics. The authors also note that Europe and Asia are beginning to address solid fuel issues as a consolidated discipline. This pattern should be helpful in broadening the understanding of solid fuels combustion processes and in ferreting out erroneous data and conclusions. This is important in view of the recent concern about the role of low dioxin exposure levels on fetal development and the immune system.

  10. 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.

  11. Determination of organic compounds in medicinal plants, commercialized in capsulated forms and 'in natura' by wavelength dispersive X-ray fluorescence spectrometry (WDXRF). Determination of quantitative inorganic profiles; Determinacao de componentes organicos em plantas medicinais, comercializadas em forma de po (capsulas) e 'in natura', utilizando a tecnica de fluorescencia de raios X por dispersao de comprimento de onda (WDXRF). Determinacao de perfis inorganicos quantitativos

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Manuel Octavio M.; Sato, Ivone Mulako; Salvador, Vera Lucia R. [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil). Centro de Quimica e Meio Ambiente]. E-mail: lawless@usp.br

    2005-07-01

    X-ray fluorescence technique was used to determine major and trace elements for five Brazilian commercial medicinal plants. The bromobutane (Barbatimao), Ginkgo folium (Ginkgo biloba), Echinodorus macrophyllus (Chapeu de couro), Valeriana officinalis (Valeriana), Cordia salicifolia (Porangaba) samples were collected from three to six different commercial suppliers. The species were collected 'in natura' (leaves, flowers, barks and roots) and capsulated forms. The samples were grinded in liquid N{sub 2} atmosphere and double layer pressed pellet were prepared. The elements Na, Mg, P, S, Cl, K, Ca, Mn, Fe, Ni, Cu, Zn, Rb e Sr concentrations were determined by individual calibration curves. The precision and accuracy of method were evaluated by certified reference material, NIST 1547 - Peach Leaves and the Chauvenet, Cochrane, ANOVA and Z-score statistical tests were applied. Each specimen presented a distinct inorganic profile and a great variation in its composition was observed. The inorganic profile will contribute for the elaboration of a quality and security guide to assure the phytotherapics commercialization. Moreover, these profiles could be used as complementary data to active farmaco compounds profiles for specimen's ratification. (author)

  12. Inorganic Nanotubes and Fullerene-Like Nanoparticles:. from the Lab to the Market Place

    Science.gov (United States)

    Tenne, R.

    2013-05-01

    Layered compounds, like MoS2 were shown by the author to be unstable in the nano-regime. Using new chemical strategies, closed-cage hollow nanostructures in the form of inorganic fullerene-like nanoparticles and inorganic nanotubes were synthesized. These nanostructures exhibit numerous interesting physico-chemical properties and are employed as superior solid lubricants, with numerous other applications currently being developed.

  13. 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)

  14. 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.

  15. Organic - Inorganic Hybrids made from Polymerizable Precursors

    NARCIS (Netherlands)

    Uricanu, V.I.; Donescu, D.; Banu, A.G.; Serban, S.; Olteanu, M.; Dudau, M.

    2004-01-01

    Organic–inorganic hybrid films were prepared based on a recipe using organoalkoxysilanes’ ability to create an inorganic network combined with polymer network formation via radical polymerization of the organic groups. The starting mixtures included different triethoxysilanes (RTES), where the

  16. Energy Consumption and Carbon Dioxide Emissions of China’s Non-Metallic Mineral Products Industry: Present State, Prospects and Policy Analysis

    Directory of Open Access Journals (Sweden)

    Hui Hu

    2014-11-01

    Full Text Available China is the largest non-metallic mineral producer in the world and one of the key consumers of four major non-metallic mineral products, including cement, refractories, plate glass and ceramics. The non-metallic mineral products industry’s rapid growth has brought about a large demand for energy. The present study provides an overview of China’s non-metallic mineral products industry in terms of production, energy consumption and carbon dioxide emissions. In this industry, the energy efficiency is relatively low and the level of carbon dioxide emission is much higher than developed countries’ average. This study interprets the effects of some newly issued policies and analyses the influential factors in achieving energy conservation and emission reduction goals. It also discusses the prospects for saving energy and emission reduction in the industry. Retrofitting facilities and using new production technologies is imperative. Additionally, implementing market-based policies, promoting industrial transformation and effective international cooperation would help decrease carbon dioxide emissions and energy consumption.

  17. Effect of Calcium Treatment on Non-Metallic Inclusions in Ultra-Low Oxygen Steel Refined by High Basicity High Al2O3 Sla

    Institute of Scientific and Technical Information of China (English)

    YANG Jun; WANG Xin-hua; JIANG Min; WANG Wan-jun

    2011-01-01

    The influence of calcium treatment on non-metallic inclusions had been studied when control technology of refining top slag in ladle furnace was used in ultra-low oxygen steelmaking. A sufficient amount aluminium was added to experimental heats for final

  18. Effect of the structural parameters changes in the multi-strand tundish on the non-metallic inclusions distribution and separation

    Directory of Open Access Journals (Sweden)

    M. Warzecha

    2014-10-01

    Full Text Available The aim of presented studies was to investigate the fluid flow change and non-metallic inclusions removal changes due to tundish construction modifications. In presented study, numerical simulations were used. Numerical simulations are carried out with the finite-volume commercial code ANSYS Fluent. Steady-state casting conditions for the flow structure and the inclusions removal process are analysed.

  19. Mixed chloride/phosphine complexes of the dirhenium core. 10. Redox reactions of an edge-sharing dirhenium(III) non-metal-metal-bonded complex, Re(2)(mu-Cl)(2)Cl(4)(PMe(3))(4).

    Science.gov (United States)

    Cotton, F A; Dikarev, E V; Petrukhina, M A

    2001-12-17

    Reduction and oxidation reactions of the dirhenium(III) non-metal-metal-bonded edge-sharing complex, Re(2)(mu-Cl)(2)Cl(4)(PMe(3))(4) (1), have been studied. Several new mono- and dinuclear rhenium compounds have been isolated and structurally characterized in the course of this study. Reductions of 1 with 1 and 2 equiv of KC(8) result in an unusual face-sharing complex having an Re(2)(5+) core, Re(2)(mu-Cl)(3)Cl(2)(PMe(3))(4) (2), and a triply bonded Re(II) compound, 1,2,7,8-Re(2)Cl(4)(PMe(3))(4) (3), respectively. Two-electron reduction of 1 in the presence of tetrabutylammonium chloride affords a new triply bonded complex of the Re(2)(4+) core, [Bu(n)()(4)N][1,2,7-Re(2)Cl(5)(PMe(3))(3)] (4). Oxidation of 1 with NOBF(4) yields a Re(IV) mononuclear compound, trans-ReCl(4)(PMe(3))(2) (5). Two isomers of the monomeric Re(III) anion, [ReCl(4)(PMe(3))(2)](-) (6, 7), have been isolated as side products. The crystal structures of compounds 2 and 4-7 have been determined by X-ray crystallography. The Re-Re distance in the face-sharing complex 2 of 2.686(1) A is relatively short. The metal-metal bond length in anion 4 of 2.2354(7) A is consistent with the usual values for the triply bonded Re(2)(4+) core compounds. In addition, a cis arrangement of trimethylphosphine ligands in the starting material 1 is retained upon reduction in the dinuclear products 2-4.

  20. 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.

  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. Deformation and fracture properties of metals with non-metallic inclusions; Verformung und Bruch von Metallen mit nichtmetallischen Einschluessen

    Energy Technology Data Exchange (ETDEWEB)

    Schmauder, S.; Soppa, E. [Stuttgart Univ. (Germany). Staatliche Materialpruefungsanstalt

    1998-12-31

    Microstructural effects due to formation of non-uniform lines of non-metallic inclusions in the matrix are examined with respect to their macro-, meso-, and micromechanical effects in the alloy Al(6061) reinforced by SiC inclusions. A comparative analysis of results obtained with various microstructures reveals essential differences in the formation of shear bands, stress peaks, and strain concentrations in the material structure. The maxima and the distribution of those field variables are determined not only by the arrangement of inclusions clusters in the stringers but also depend on the presence and number of single-particle inclusions in pure matrix material. The banding of the microstructure causes a strongly anisotropic behaviour in terms of stress and strain distributions. (orig./CB) [Deutsch] In diesem Beitrag werden Gefuegeeinfluesse aufgrund unterschiedlich starker zeiliger Anordnungen der Teilchen in der Matrix im Hinblick auf ihre makro-, meso- und mikromechanischen Auswirkungen am Beispiel einer SiC-teilchenverstaerkten Aluminiumlegierung Al(6061) untersucht. Ein Vergleich der Ergebnisse verschiedener Gefuege zeigt wesentliche Unterschiede hinsichtlich der Ausbildung von Scherbaendern, Spannungsspitzen und von Dehnungskonzentrationen im Werkstoffgefuege. Die Maxima und die Verteilung dieser Feldgroessen sind nicht nur abhaengig davon, wie die Teilchen in den Zeilen angeordnet sind, sondern auch davon, ob einzelne Teilchen in reinen Matrixbereichen vorhanden sind. Die Zeiligkeit des Gefueges fuehrt zu einem stark anisotropen Verhalten hinsichtlich Spannungs- und Dehnungsverteilungen. (orig.)

  3. Assessment of Different Turbulence Models for the Motion of Non-metallic Inclusion in Induction Crucible Furnace

    Science.gov (United States)

    Barati, H.; Wu, M.; Kharicha, A.; Ludwig, A.

    2016-07-01

    Turbulent fluid flow due to the electromagnetic forces in induction crucible furnace (ICF) is modeled using k-ɛ, k-ω SST and Large Eddy Simulation (LES) turbulence models. Fluid flow patterns calculated by different turbulence models and their effects on the motion of non-metallic inclusions (NMI) in the bulk melt have been investigated. Results show that the conventional k-ɛ model cannot solve the transient flow in ICF properly. With k-ω model transient flow and oscillation behavior of the flow pattern can be solved, and the motion of NMI can be tracked fairly well. LES model delivers the best modeling result on both details of the transient flow pattern and motion trajectories of NMI without the limitation of NMI size. The drawback of LES model is the long calculation time. Therefore, for general purpose to estimate the dynamic behavior of NMI in ICF both k-ω SST and LES are recommended. For the precise calculation of the motion of NMI smaller than 10 μm only LES model is appropriate.

  4. Effectiveness of Shot Peening In Suppressing Fatigue Cracking At Non-Metallic Inclusions In Udimet(Registered Trademark)720

    Science.gov (United States)

    Barrie, Robert L.; Gabb, Timothy P.; Telesman, Jack; Kantzos, Peter T.; Prescenzi, Anthony; Biles, T.; Bonacuse, P. J.

    2006-01-01

    The fatigue lives of modern powder metallurgy disk alloys can be reduced over an order of magnitude by cracking at inherent non-metallic inclusions. The objective of this work was to study the effectiveness of shot peening in suppressing LCF crack initiation and growth at surface nonmetallic inclusions. Inclusions were carefully introduced at elevated levels during powder metallurgy processing of the nickel-base disk superalloy Udimet 720. Multiple strain-controlled fatigue tests were then performed on machined specimens with and without shot peened test sections at 427 C and 650 C. The low cycle fatigue lives and failure initiation sites varied as functions of inclusion content, shot peening, and fatigue conditions. A large majority of the failures in as-machined specimens with the introduced inclusions occurred at cracks initiating from inclusions intersecting the specimen surface. These inclusions reduced fatigue life by up to 100X, when compared to lives of material without inclusions residing at specimen surface. Large inclusions produced the greatest reductions in life for tests at low strain ranges and high strain ratios. Shot peening improved life in many cases by reducing the most severe effects of inclusions.

  5. Effectiveness of Shot Peening in Suppressing Fatigue Cracking at Non-Metallic Inclusions in Udimet(trademark) 720

    Science.gov (United States)

    Barrie, Robert L.; Gabb, Timothy P.; Telesman, Jack; Kantzos, Peter T.; Prescenzi, Anthony; Biles, Tiffany; Bonacuse, Peter J.

    2005-01-01

    The fatigue lives of modern powder metallurgy disk alloys can be reduced by over an order of magnitude by surface cracking at inherent non-metallic inclusions. The objective of this work was to study the effectiveness of shot peening in suppressing LCF crack initiation and growth at surface nonmetallic inclusions. Inclusions were carefully introduced at elevated levels during powder metallurgy processing of the nickel-base disk superalloy Udimet 720. Multiple strain-controlled fatigue tests were then performed on machined specimens at 427 and 650 C in peened and unpeened conditions. Analyses were performed to compare the low cycle fatigue lives and failure initiation sites as a function of inclusion content, shot peening, and fatigue conditions. A large majority of the failures in as-machined specimens with introduced inclusions occurred at cracks initiating from inclusions intersecting the specimen surface. The inclusions could reduce fatigue life by up to 100X. Large inclusions had the greatest effect on life in tests at low strain ranges and high strain ratios. Shot peening can be used to improve life in these conditions by reducing the most severe effects of inclusions.

  6. 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.

  7. Nomenclature of chemical compounds

    Directory of Open Access Journals (Sweden)

    Karolina Kaczmarek

    2009-01-01

    Full Text Available This article presents the mechanisms of the inorganic chemistry nomenclature formation in French language. It shows the structure and the way of presenting the names of chemical compounds either descriptively or by giving the structural formulas’ characteristics, their transcription and order of reading the letters. The text specifies the rules of naming a chemical compound, according to the criteria of IUPAC (Union of Pure and Applied Chemistry, the organisation responsible for digesting the chemical nomenclature. The article contains the transcription chart and the manner of reading the structural formula, also called latero-numerical. Additionally, there is information conceming the usage of the common names given, still remaining in use next to the names compatible with those of IUPAC. Particular types of chemical compounds have served as models for description of other nomenclature formation rules from the simplest structures to the complicated compound ones. A short summary presents the relations and similarities between the names of particular types of chemical compounds.

  8. A novel lattice energy calculation technique for simple inorganic crystals

    Energy Technology Data Exchange (ETDEWEB)

    Kaya, Cemal [Department of Chemistry, Faculty of Science, Cumhuriyet University, 58140 Sivas (Turkey); Kaya, Savaş, E-mail: savaskaya@cumhuriyet.edu.tr [Department of Chemistry, Faculty of Science, Cumhuriyet University, 58140 Sivas (Turkey); Banerjee, Priyabrata [Surface Engineering and Tribology Group, CSIR-Central Mechanical Engineering Research Institute, Mahatma Gandhi Avenue, Durgapur 713209 (India)

    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.

  9. 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.

  10. Organic-inorganic hybrid polymer-encapsulated magnetic nanobead catalysts.

    Science.gov (United States)

    Arai, Takayoshi; Sato, Toru; Kanoh, Hirofumi; Kaneko, Katsumi; Oguma, Koichi; Yanagisawa, Akira

    2008-01-01

    A new strategy for the encapsulation of magnetic nanobeads was developed by using the in situ self-assembly of an organic-inorganic hybrid polymer. The hybrid polymer of {[Cu(bpy)(BF(4))(2)(H(2)O)(2)](bpy)}(n) (bpy=4,4'-bipyridine) was constructed on the surface of amino-functionalized magnetic beads and the resulting hybrid-polymer-encapsulated beads were utilized as catalysts for the oxidation of silyl enolates to provide the corresponding alpha-hydroxy carbonyl compounds in high yield. After the completion of the reaction, the catalyst was readily recovered by magnetic separation and the recovered catalyst could be reused several times. Because the current method did not require complicated procedures for incorporating the catalyst onto the magnetic beads, the preparation and the application of various other types of organic-inorganic hybrid-polymer-coated magnetic beads could be possible.

  11. The effect of non-metallic inclusions on the fracture toughness master curve in high copper reactor pressure vessel welds

    Science.gov (United States)

    Oh, Yong-Jun; Lee, Bong-Sang; Hong, Jun-Hwa

    2002-03-01

    The fracture toughness of two high copper reactor pressure vessel welds having low upper shelf energy was evaluated in accordance with the master curve method of ASTM E1921. The resultant data were correlated to the metallurgical factors involved in the brittle fracture initiation to provide a metallurgical-based understanding of the master curve. The tests were performed using pre-cracked Charpy V-notched specimens and the master curve was made with an average of T0 values determined at different temperatures. In all specimens, the cleavage fracture initiated at non-metallic inclusion ranging from 0.7 to 3.5 μm in diameter showing a scatter with the specimens and testing temperatures. Temperature dependency of the triggering particle size was not found. The fracture toughness ( KJC) was inversely proportional to the square root of the triggering inclusion diameter ( di) at respective temperatures. From this relationship, we determined median KJC values which correspond to the average value of triggering inclusion diameter of all tested specimens and defined them as a modified median KJC ( K'JC(med) ). The obtained K'JC(med) values showed quite smaller deviation from the master curve at different temperatures than the experimental median KJC values. This suggests that the master curve is on the premise of a constant dimension of key microstructural factor in a material regardless of the testing temperature. But the inclusion size at trigger point played an important role in the absolute position of the master curve with temperature and the consequent T0 value.

  12. The effect of non-metallic inclusions on the fracture toughness master curve in high copper reactor pressure vessel welds

    Energy Technology Data Exchange (ETDEWEB)

    Oh, Yong-Jun E-mail: yjoh@kaeri.re.kr; Lee, Bong-Sang; Hong, Jun-Hwa

    2002-03-01

    The fracture toughness of two high copper reactor pressure vessel welds having low upper shelf energy was evaluated in accordance with the master curve method of ASTM E1921. The resultant data were correlated to the metallurgical factors involved in the brittle fracture initiation to provide a metallurgical-based understanding of the master curve. The tests were performed using pre-cracked Charpy V-notched specimens and the master curve was made with an average of T{sub 0} values determined at different temperatures. In all specimens, the cleavage fracture initiated at non-metallic inclusion ranging from 0.7 to 3.5 {mu}m in diameter showing a scatter with the specimens and testing temperatures. Temperature dependency of the triggering particle size was not found. The fracture toughness (K{sub J{sub C}}) was inversely proportional to the square root of the triggering inclusion diameter (d{sub i}) at respective temperatures. From this relationship, we determined median K{sub J{sub C}} values which correspond to the average value of triggering inclusion diameter of all tested specimens and defined them as a modified median K{sub J{sub C}} (K{sup '}{sub J{sub C}}{sub (med)}). The obtained K{sup '}{sub J{sub C}}{sub (med)} values showed quite smaller deviation from the master curve at different temperatures than the experimental median K{sub J{sub C}} values. This suggests that the master curve is on the premise of a constant dimension of key microstructural factor in a material regardless of the testing temperature. But the inclusion size at trigger point played an important role in the absolute position of the master curve with temperature and the consequent T{sub 0} value.

  13. Tunable electronic structures of germanium monochalcogenide nanosheets via light non-metallic atom functionalization: a first-principles study.

    Science.gov (United States)

    Ding, Yi; Wang, Yanli

    2016-08-17

    Germanium monochalcogenides, i.e. GeS and GeSe sheets, are isoelectronic analogues of phosphorene, which have been synthesized in recent experiments (P. Ramasamy et al., J. Mater. Chem. C, 2016, 4, 479). Utilizing first-principles calculations, we have investigated their tunable electronic and magnetic properties via light non-metallic atom (B, C, N, O, Si, P, S) functionalization. We find that on these GeS and GeSe sheets O and S adatoms prefer to locate at the top site above the Ge atom, while the other ones like to occupy the anion site, which push the original S/Se atom to the hollow site instead. O and S adatoms slightly affect the semiconducting behaviour of the doped systems, while B, C, N, Si, P ones will drastically modify their band structures and induce versatile spintronic properties. Through the supercell calculations, B and C adatoms are found to induce a bipolar semiconducting behaviour in the decorated systems, while the N/P adatom will cause a spin-gapless-semiconducting/nearly-half-metallic feature in them. The B/C/N/Si/P-substituted GeS/GeSe sheet can be formed by removing the hollow-site S/Se atom from the adatom-decorated structures, which exhibit an opposite semiconducting/metallic behaviour to their phosphorene counterparts. A general odd-even rule is proposed for this phenomenon, which shows that an odd (even) number of valence electron difference between the substitution and host atoms would cause a metallic (semiconducting) feature in the substituted systems. Our study demonstrates that atom functionalization is an efficient way to tailor the properties of GeS and GeSe nanosheets, which have adaptable electronic properties for potential applications in nanoelectronics and spintronics.

  14. 废弃电路板中非金属组分的回收利用%Recycling of non-metallic fractions from waste printed circuit boards

    Institute of Scientific and Technical Information of China (English)

    刘旸; 刘静欣; 江晓健; 郭学益

    2016-01-01

    废弃电路板是电子废弃物的重要组成部分。目前工业生产及工艺开发多针对极具经济回收价值的电路板金属组分。然而,占电路板质量分数70%的非金属组分却关注较少。文章分析了废弃电路板非金属组分的组成及其有害组分,其含有树脂及玻璃纤维等有价成分和溴、夹杂重金属等污染环境的物质,其回收利用对于资源循环利用及环境保护均有重要意义。非金属组分回收利用主要有物理处理和化学处理2种技术:物理处理技术主要将非金属组分用作结构材料填料、塑料改性剂和建筑材料改性剂;化学处理技术通过焚烧将非金属组分用作燃料和熔剂或通过热解回收或溶剂分解回收可将非金属组分转化为化工产品。这2种技术在非金属组分资源化利用上各有优势,都已有部分工业化应用。%Waste printed circuit boards (WPCBs) are important parts in the electronic waste. Nowadays, recov-ering metals from WPCBs are developed but non-metallic fractions which accounts for 70% of waste printed circuit boards have not been effectively utilized. The non-metallic fractions and hazards in waste printed cir-cuit boards were analyzed in this paper. The results show that resins and glass fiber in non-metallic fractions can be recycled and bromine and heavy metals could pollute environment. Recovering non-metallic fractions are important to recycling and environment, which can be divided into physical recycling technology and chemical recycling technology, with the formal using non-metallic fractions as the filler materials, plastic modifier or building material modifiers, and the latter using non-metallic fractions as the fuel and smelting flux through incineration or convert non-metallic fractions into chemical products through pyrolysis or solvent decomposition. Both technologies have their own advantages in resource utilization of non-metallic fractions, and partly

  15. The Influence of Technological Parameters of X70 Stainless Steel Ladle Refining on the Residual Content of Non-Metallic Inclusions

    Directory of Open Access Journals (Sweden)

    Babanin A.

    2015-09-01

    Full Text Available It is demonstrated that during secondary refining at the ladle furnace the carbon content of steel and the residence time of the metal in the ladle exert a significant impact on the residual content of non-metallic inclusions (NMI in steel. Mathematical calculations showed that the dynamic forces have minor effect on the motion of small sized NMI, making it difficult to penetrate deep into the slag.

  16. 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

  17. 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.

  18. Study of the physicochemical effects on the separation of the non-metallic fraction from printed circuit boards by inverse flotation.

    Science.gov (United States)

    Flores-Campos, R; Estrada-Ruiz, R H; Velarde-Sánchez, E J

    2017-09-06

    Recycling printed circuit boards using green technology is increasingly important due to the metals these contain and the environmental care that must be taken when separating the different materials. Inverse flotation is a process that can be considered a Green Technology, which separates metallic from non-metallic fractions. The degree of separation depends on how much material is adhered to air bubbles. The contact angle measurement allows to determine, in an easy way, whether the flotation process will occur or not and thus establish a material as hydrophobic or not. With the material directly obtained from the milling process, it was found that the contact angle of the non-metallic fraction-liquid-air system increases as temperature increases. In the same way, the increments in concentration of frother in the liquid increase the contact angle of the non-metallic fraction-liquid-air system. 10ppm of Methyl Isobutyl Carbinol provides the highest contact angle as well as the highest material charging in the bubble. Copyright © 2017. Published by Elsevier Ltd.

  19. Preparation and Characterization of Inorganic PCM Microcapsules by Fluidized Bed Method

    Directory of Open Access Journals (Sweden)

    Svetlana Ushak

    2016-01-01

    Full Text Available The literature shows that inorganic phase change materials (PCM have been very seldom microencapsulated, so this study aims to contribute to filling this research gap. Bischofite, a by-product from the non-metallic industry identified as having good potential to be used as inorganic PCM, was microencapsulated by means of a fluidized bed method with acrylic as polymer and chloroform as solvent, after compatibility studies of both several solvents and several polymers. The formation of bischofite and pure MgCl2·6H2O microcapsules was investigated and analyzed. Results showed an efficiency in microencapsulation of 95% could be achieved when using 2 min of fluidization time and 2 kg/h of atomization flow. The final microcapsules had excellent melting temperatures and enthalpy compared to the original PCM, 104.6 °C and 95 J/g for bischofite, and 95.3 and 118.3 for MgCl2·6H2O.

  20. Heat-resistant inorganic binders.

    Directory of Open Access Journals (Sweden)

    KUDRYAVTSEV Pavel Gennadievich,

    2017-04-01

    Full Text Available The authors consider some aspects of production of inorganic heat-resistant composite materials in which new classes of inorganic binders - the basic salts of various metals – are applied. The possibility to use hydroxochlorides and hydroxonitrates of aluminum, zirconium, chromium and a number of other metals as the binder has been shown. The main products of the thermal decomposition of all types of binders discussed in this paper are nano-dispersed highly refractory oxides. Increased pressure in the manufacture of these materials shifts the position of the minimum of the dependence «production strength – production temperature» in the direction of low temperatures. This effect is caused by decreased film thickness of the binder located between filler particles and hence by increased rate of transfer of the matter to the interface and by facilitated sintering process. Materials based on the systems containing chromium and some other elements in transitional oxidation states are colour. For this reason, they have the worst thermal conductivity under the same heat resistance compared to colorless materials.

  1. 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)

  2. A Simple Method for the Calculation of Lattice Energies of Inorganic Ionic Crystals Based on the Chemical Hardness.

    Science.gov (United States)

    Kaya, Savaş; Kaya, Cemal

    2015-09-08

    This paper presents a new technique for estimation of lattice energies of inorganic ionic compounds using a simple formula. This new method demonstrates the relationship between chemical hardness and lattice energies of ionic compounds. Here chemical hardness values of ionic compounds are calculated via our molecular hardness equation. The results obtained using the present method and comparisons made by considering experimental data and the results from other theoretical methods in the literature showed that the new method allows easy evaluation of lattice energies of inorganic ionic crystals without the need for ab initio calculations and complex calculations.

  3. Targeting Platinum Compounds: synthesis and biological activity

    OpenAIRE

    VAN ZUTPHEN, Steven

    2005-01-01

    Inspired by cisplatin, the inorganic drug discovered by Barnett Rosenberg in 1965, the research described in this thesis uses targeting ligands, or ligands varied in a combinatorial fashion, to find platinum complexes with more specific modes of action. These studies have lead to the development of novel (solid-phase) synthetic methods and to the discovery of several compounds with promising biological properties.

  4. 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 ...

  5. 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.

  6. 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.

  7. 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

  8. Metal nanoparticle deposited inorganic nanostructure hybrids, uses thereof and processes for their preparation

    Science.gov (United States)

    Tenne, Reshef; Tsverin, Yulia; Burghaus, Uwe; Komarneni, Mallikharjuna Rao

    2016-01-26

    This invention relates to a hybrid component comprising at least one nanoparticle of inorganic layered compound (in the form of fullerene-like structure or nanotube), and at least one metal nanoparticle, uses thereof as a catalyst, (e.g. photocatalysis) and processes for its preparation.

  9. 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

  10. An investigation of the transmethylation reaction of the methyltin chlorides with inorganic mercury

    OpenAIRE

    Brennan, Deirdre Anne

    2003-01-01

    This work explores the consequences of the reaction between methyltin compounds and inorganic mercury which is thought to occur in the environment. This reaction has considerable environmental importance. The introduction of organotin compounds into the environment may occur as a result of their use in various commercial products, including agricultural biocides. In this case the organotin species is applied directly into the environment. Once they have entered the environment their persi...

  11. Synthesis, Crystal Structure, and Characterization of a New Organic-Inorganic Hybrid Material:

    OpenAIRE

    Hela Ferjani; Habib Boughzala; Ahmed Driss

    2013-01-01

    The title compound is an organic-inorganic hybrid material. The single crystal X-ray diffraction investigation reveals that the studied compound crystallizes in the orthorhombic system, space group Pbca with the following lattice parameters:  (4) Å,  (3) Å,  (6) Å, and . The crystal lattice is composed of a discrete anion surrounded by piperazinium cations, chlorine anions, and water molecules. Complex hydrogen bonding interactions between , , organic cations, and water molecules form a thre...

  12. 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

  13. Inorganic bromine in the marine boundary layer: a critical review

    Directory of Open Access Journals (Sweden)

    R. Sander

    2003-01-01

    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 substantially depleted in bromine (often exceeding 50% relative to conservative tracers, whereas marine submicrometer aerosol is often enriched in bromine. Model calculations, laboratory studies, and field observations strongly suggest that the supermicrometer 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. Mechanisms for the submicrometer enrichments are not well understood. Currently available techniques cannot reliably quantify many 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 outside 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

  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. 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...

  16. 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...

  17. Organic and inorganic mercurials have distinct effects on cellular thiols, metal homeostasis, and Fe-binding proteins in Escherichia coli

    OpenAIRE

    LaVoie, Stephen P.; Mapolelo, Daphne T.; Cowart, Darin M.; Polacco, Benjamin J.; Johnson, Michael K.; Scott, Robert A.; Miller, Susan M.; Summers, Anne O.

    2015-01-01

    The protean chemical properties of the toxic metal mercury (Hg) have made it attractive in diverse applications since antiquity. However, growing public concern has led to an international agreement to decrease its impact on health and the environment. During a recent proteomics study of acute Hg exposure in E. coli, we also examined the effects of inorganic and organic Hg compounds on thiol- and metal- homeostases. On brief exposure, lower concentrations of divalent inorganic mercury Hg(II) ...

  18. 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.

  19. The Diesel Exhaust in Miners Study: IV. Estimating historical exposures to diesel exhaust in underground non-metal mining facilities.

    Science.gov (United States)

    Vermeulen, Roel; Coble, Joseph B; Lubin, Jay H; Portengen, Lützen; Blair, Aaron; Attfield, Michael D; Silverman, Debra T; Stewart, Patricia A

    2010-10-01

    We developed quantitative estimates of historical exposures to respirable elemental carbon (REC) for an epidemiologic study of mortality, including lung cancer, among diesel-exposed miners at eight non-metal mining facilities [the Diesel Exhaust in Miners Study (DEMS)]. Because there were no historical measurements of diesel exhaust (DE), historical REC (a component of DE) levels were estimated based on REC data from monitoring surveys conducted in 1998-2001 as part of the DEMS investigation. These values were adjusted for underground workers by carbon monoxide (CO) concentration trends in the mines derived from models of historical CO (another DE component) measurements and DE determinants such as engine horsepower (HP; 1 HP = 0.746 kW) and mine ventilation. CO was chosen to estimate historical changes because it was the most frequently measured DE component in our study facilities and it was found to correlate with REC exposure. Databases were constructed by facility and year with air sampling data and with information on the total rate of airflow exhausted from the underground operations in cubic feet per minute (CFM) (1 CFM = 0.0283 m³ min⁻¹), HP of the diesel equipment in use (ADJ HP), and other possible determinants. The ADJ HP purchased after 1990 (ADJ HP₁₉₉₀(+)) was also included to account for lower emissions from newer, cleaner engines. Facility-specific CO levels, relative to those in the DEMS survey year for each year back to the start of dieselization (1947-1967 depending on facility), were predicted based on models of observed CO concentrations and log-transformed (Ln) ADJ HP/CFM and Ln(ADJ HP₁₉₉₀(+)). The resulting temporal trends in relative CO levels were then multiplied by facility/department/job-specific REC estimates derived from the DEMS surveys personal measurements to obtain historical facility/department/job/year-specific REC exposure estimates. The facility-specific temporal trends of CO levels (and thus the REC

  20. Comparison of Bioavailability and Biotransformation of Inorganic and Organic Arsenic to Two Marine Fish.

    Science.gov (United States)

    Zhang, Wei; Wang, Wen-Xiong; Zhang, Li

    2016-03-01

    Dietary uptake could be the primary route of arsenic (As) bioaccumulation in marine fish, but the bioavailability of inorganic and organic As remains elusive. In this study, we investigated the trophic transfer and bioavailability of As in herbivorous rabbitfish Siganus fuscescens and carnivorous seabass Lateolabrax japonicus. Rabbitfish were fed with one artificial diet or three macroalgae, whereas seabass were fed with one artificial diet, one polychaete, or two bivalves for 28 days. The six spiked fresh prey diets contained different proportions of inorganic As [As(III) and As(V)] and organic As compounds [methylarsenate (MMA), dimethylarsenate (DMA), and arsenobetaine (AsB)], and the spiked artificial diet mainly contained As(III) or As(V). We demonstrated that the trophic transfer factors (TTF) of As in both fish were negatively correlated with the concentrations of inorganic As in the diets, while there was no relationship between TTF and the AsB concentrations in the diets. Positive correlation was observed between the accumulated As concentrations and the AsB concentrations in both fish, suggesting that organic As compounds (AsB) were more trophically available than inorganic As. Furthermore, the biotransformation ability of seabass was higher than that in rabbitfish, which resulted in higher As accumulation in seabass than in rabbitfish. Our study demonstrated that different prey with different inorganic/organic As proportions resulted in diverse bioaccumulation of total As in different marine fish.

  1. 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

    2017-01-01

    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. PMID:28212297

  2. 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.

  3. 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.

  4. 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

  5. Effect of inhomogeneous distribution of non-metallic inclusions on crack path deflection in G42CrMo4 steel at different loading rates

    Directory of Open Access Journals (Sweden)

    S. Henschel

    2015-10-01

    Full Text Available An inhomogeneous distribution of non-metallic inclusions can result from the steel casting process. The aim of the present study was to investigate the damaging effect of an inhomogeneous distribution of nonmetallic inclusions on the crack extension behavior. To this end, the fracture toughness behavior in terms of quasi-static J-a curves was determined at room temperature. Additionally, dynamic fracture mechanics tests in an instrumented Charpy impact-testing machine were performed. The fracture surface of fracture mechanics specimens was analyzed by means of scanning electron microscopy. It was shown that an inhomogeneous distribution significantly affected the path and, therefore, the plane of crack growth. Especially clusters of non-metallic inclusions with a size of up to 200 μm exhibited a very low crack growth resistance. Due to the damaging effect of the clusters, the growing crack was strongly deflected towards the cluster. Furthermore, crack tip blunting was completely inhibited when inclusions were located at the fatigue precrack tip. Due to the large size of the non-metallic inclusion clusters, the height difference introduced by crack path deflection was significantly larger than the stretch zone height due to the crack tip blunting. However, the crack path deflection introduced by a cluster was not associated with a toughness increasing mechanism. The e dynamic loading ( 1 0.5 5 s MPam 10   K did not result in a transition from ductile fracture to brittle fracture. However, the crack growth resistance decreased with increased loading rate. This was attributed to the higher portion of relatively flat regions where the dimples were less distinct.

  6. Effect Of Non-metal Elements (C, N, S) As Anionic Dopants On Electronic Structure Of Tio2-Anatase By Density-Functional Theory Approach

    OpenAIRE

    Hari Sutrisno

    2016-01-01

    This article is a theoritical approach to calculate the electronic structure of undoped- and non-metal anions doped-TiO2-anatase. The objective of the research is to calculate abinitio the band structure and the density of states (DOS) of undoped-, C-, N-, and S-doped TiO2-anatase. Kohn-Sham equations are performed with the density functional theory (DFT) using the local density approximation (LDA) for exchange-correlation functional. The first-principle calculations were done using supercell...

  7. 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

    collected in the official EU food control today are reported as total arsenic. High Performance Liquid Chromatography Inductively Coupled Plasma Mass Spectrometry (HPLC-ICP-MS) is a useful but expensive tool for metal speciation analysis. Our novel, simple and inexpensive method for determination...... 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...

  8. Electrochemical Catalysis of Inorganic Complex K4[Fe(CN)6] by Shewanella oneidensis MR-1

    DEFF Research Database (Denmark)

    Zheng, Zhiyong; Wu, Ranran; Xiao, Yong

    to the redox proteins localized to the outer-membrane, for example, the MtrC, MtrB,MtrA and CymA2. Here we investigate its electrochemical properties towards redox inorganic redox compounds. It shows strong electrocatalysis toward electrochemical oxidation of K4[Fe(CN)6]. As a redox molecule, K4[Fe(CN)6] gives...... on the selectivity and electrocatalysis mechanisms of Shewanella oneidensis MR-1 are under investigation. The ability of Shewanella oneidensis MR-1 to catalyze redox action of inorganic metal complex compounds will provide an insight on metal cycles in nature....... disappearance of the cathodic peak and strengthen of the anodic peak, which is a typical catalysis feature of electrochemical oxidation. Further experiments show that Shewanella oneidensis MR-1 does not give such electrocatalysis to redox compounds such as Ru[(NH3)6]Cl3 and Resorufin. Systematic study...

  9. 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

  10. 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.

  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. P. brasiliensis Virulence Is Affected by SconC, the Negative Regulator of Inorganic Sulfur Assimilation

    Science.gov (United States)

    Menino, João Filipe; Saraiva, Margarida; Gomes-Rezende, Jéssica; Sturme, Mark; Pedrosa, Jorge; Castro, António Gil; Ludovico, Paula; Goldman, Gustavo H.; Rodrigues, Fernando

    2013-01-01

    Conidia/mycelium-to-yeast transition of Paracoccidioidesbrasiliensis is a critical step for the establishment of paracoccidioidomycosis, a systemic mycosis endemic in Latin America. Thus, knowledge of the factors that mediate this transition is of major importance for the design of intervention strategies. So far, the only known pre-requisites for the accomplishment of the morphological transition are the temperature shift to 37°C and the availability of organic sulfur compounds. In this study, we investigated the auxotrophic nature to organic sulfur of the yeast phase of Paracoccidioides, with special attention to P. brasiliensis species. For this, we addressed the role of SconCp, the negative regulator of the inorganic sulfur assimilation pathway, in the dimorphism and virulence of this pathogen. We show that down-regulation of SCONC allows initial steps of mycelium-to-yeast transition in the absence of organic sulfur compounds, contrarily to the wild-type fungus that cannot undergo mycelium-to-yeast transition under such conditions. However, SCONC down-regulated transformants were unable to sustain yeast growth using inorganic sulfur compounds only. Moreover, pulses with inorganic sulfur in SCONC down-regulated transformants triggered an increase of the inorganic sulfur metabolism, which culminated in a drastic reduction of the ATP and NADPH cellular levels and in higher oxidative stress. Importantly, the down-regulation of SCONC resulted in a decreased virulence of P. brasiliensis, as validated in an in vivo model of infection. Overall, our findings shed light on the inability of P. brasiliensis yeast to rely on inorganic sulfur compounds, correlating its metabolism with cellular energy and redox imbalances. Furthermore, the data herein presented reveal SconCp as a novel virulence determinant of P. brasiliensis. PMID:24066151

  14. P. brasiliensis virulence is affected by SconC, the negative regulator of inorganic sulfur assimilation.

    Directory of Open Access Journals (Sweden)

    João Filipe Menino

    Full Text Available Conidia/mycelium-to-yeast transition of Paracoccidioidesbrasiliensis is a critical step for the establishment of paracoccidioidomycosis, a systemic mycosis endemic in Latin America. Thus, knowledge of the factors that mediate this transition is of major importance for the design of intervention strategies. So far, the only known pre-requisites for the accomplishment of the morphological transition are the temperature shift to 37 °C and the availability of organic sulfur compounds. In this study, we investigated the auxotrophic nature to organic sulfur of the yeast phase of Paracoccidioides, with special attention to P. brasiliensis species. For this, we addressed the role of SconCp, the negative regulator of the inorganic sulfur assimilation pathway, in the dimorphism and virulence of this pathogen. We show that down-regulation of SCONC allows initial steps of mycelium-to-yeast transition in the absence of organic sulfur compounds, contrarily to the wild-type fungus that cannot undergo mycelium-to-yeast transition under such conditions. However, SCONC down-regulated transformants were unable to sustain yeast growth using inorganic sulfur compounds only. Moreover, pulses with inorganic sulfur in SCONC down-regulated transformants triggered an increase of the inorganic sulfur metabolism, which culminated in a drastic reduction of the ATP and NADPH cellular levels and in higher oxidative stress. Importantly, the down-regulation of SCONC resulted in a decreased virulence of P. brasiliensis, as validated in an in vivo model of infection. Overall, our findings shed light on the inability of P. brasiliensis yeast to rely on inorganic sulfur compounds, correlating its metabolism with cellular energy and redox imbalances. Furthermore, the data herein presented reveal SconCp as a novel virulence determinant of P. brasiliensis.

  15. Biomedical inorganic polymers bioactivity and applications of natural and synthetic polymeric inorganic molecules

    CERN Document Server

    Müller, Werner E G; Schröder, Heinz C; Schroder, Heinz C

    2014-01-01

    In recent years, inorganic polymers have attracted much attention in nano-biomedicine, in particular in the area of regenerative medicine and drug delivery. This growing interest in inorganic polymers has been further accelerated by the development of new synthetic and analytical methods in the field of nanotechnology and nanochemistry. Examples for biomedical inorganic polymers that had been proven to exhibit biomedical effects and/or have been applied in preclinical or clinical trials are polysilicate / silica glass (such as naturally formed "biosilica" and synthetic "bioglass") and inorganic polyphosphate. Some members of the mentioned biomedical inorganic polymers have already been applied e.g. as "bioglass" for bone repair and bone tissue engineering, or they are used in food processing and in dental care (inorganic polyphosphates). However, there are a number of further biological and medicinal properties of these polymers, which have been elucidated in the last few years but not yet been applied for tr...

  16. Study of the nature of non-metallic inclusions in samples of aluminum and silicon killed low carbon steels, collected in the refining treatment and continuous casting stages

    Directory of Open Access Journals (Sweden)

    José Carlos Santos Pires

    2004-12-01

    Full Text Available The amount, distribution, size and chemical composition of non-metallic inclusions have a direct influence on steel properties. By controlling size and chemical composition of these inclusions, it is possible to get a product with good quality. The identification of the nature and the control of inclusion formation are very important for steel cleanness. The behavior of these inclusions is predictable, in some extent, by the determination of the chemical composition of non-metallic phases that form such inclusions. With the objective of studying the chemical composition, the size and the distribution of such inclusions, samples of aluminum and silicon killed low carbon steels were collected in a national steel industry in the secondary refining and continuous casting stages. These samples were analyzed in the scanning electron microscope (SEM coupled to an energy dispersive analysis system (EDS. From the results, it was possible to evaluate the nature of inclusions and to analyze the effectiveness of the refining process in the reduction of the number and area fraction of the inclusions. It was also possible to verify that the inclusions that remained after treatment, are less damage both to the steel properties as to the continuous casting process (clogging of the submerged valve.

  17. Strength and deformability of compressed concrete elements with various types of non-metallic fiber and rods reinforcement under static loading

    Science.gov (United States)

    Nevskii, A. V.; Baldin, I. V.; Kudyakov, K. L.

    2015-01-01

    Adoption of modern building materials based on non-metallic fibers and their application in concrete structures represent one of the important issues in construction industry. This paper presents results of investigation of several types of raw materials selected: basalt fiber, carbon fiber and composite fiber rods based on glass and carbon. Preliminary testing has shown the possibility of raw materials to be effectively used in compressed concrete elements. Experimental program to define strength and deformability of compressed concrete elements with non-metallic fiber reinforcement and rod composite reinforcement included design, manufacture and testing of several types of concrete samples with different types of fiber and longitudinal rod reinforcement. The samples were tested under compressive static load. The results demonstrated that fiber reinforcement of concrete allows increasing carrying capacity of compressed concrete elements and reducing their deformability. Using composite longitudinal reinforcement instead of steel longitudinal reinforcement in compressed concrete elements insignificantly influences bearing capacity. Combined use of composite rod reinforcement and fiber reinforcement in compressed concrete elements enables to achieve maximum strength and minimum deformability.

  18. 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.

  19. 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...

  20. 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.

  1. Organic free decavanadate based materials: Inorganic linkers to obtain extended structures

    Science.gov (United States)

    Yerra, Sridevi; Das, Samar K.

    2017-10-01

    Decavanadate based extended structures containing compounds [{Na3(H2O)8(μ2-H2O)6Ag2}HV10O28]n·6nH2O (1), [Co(H2O)6]n[{Na2(H2O)6(μ2-H2O)4Co(H2O)2}V10O28]n·4nH2O (2) and [Zn(H2O)6]n[{Na2(H2O)6(μ2-H2O)4Zn(H2O)2}V10O28]n·4nH2O (3) have been synthesized from respective aqueous solutions of sodium metavanadate. Compounds 1, 2 and 3 crystallize in a triclinic space group P-1. Compound 1 is a three-dimensional inorganic solid, whereas compounds 2 and 3 are isomorphous one-dimensional inorganic polymers. In the crystal structure of compound 1, the silver (I) cation is coordinated to the terminal oxygen as well as bridging oxygen atoms of decavanadate anion and it is also connected to bridging oxygen atom of trimeric sodium aqua cluster cation. In the crystals of compound 2, one hexa-hydrated cobalt cation is present as a counter cation and one ;di-sodium cobalt aqua-complex; cation is supported on the [V10O28]6- cluster anion by coordinate covalent bond. Compound 3 is isomorphous with compound 2, with Zn2+ present (in compound 3) in the place of Co2+ (in compound 2). Compounds 1, 2 and 3 are characterized by routine elemental analyses, FT-IR spectroscopy and unambiguously by single crystal X-ray crystallography. In the crystal structure of compound 1, an unusual silver dimer is observed.

  2. Fractal Dimension Study of Non-metallic Inclusion Images in Steel%钢中非金属夹杂物图像分形维数的研究

    Institute of Scientific and Technical Information of China (English)

    岳强; 张雅丽; 孔辉; 周俐; 王建军; 汪诚

    2012-01-01

    Binary images of non-metallic inclusions boundary were obtained by processing images of rolling material of 304/304L stainless steel with large inclusions and ingots with micro inclusions. Box-counting method was employed to compute fractal dimension of inclusion contour. Algorithm was implemented with MATLAB programming. Results show that the fractal dimension of inclusion is closely related to its composition and melting point. Morphologies of low melting point Al2O3-SiO2-CaO compound inclusion are sphere or similar sphere, their fractal dimensions are small, morphologies of high melting point Al2O3 inclusions and SiO2 inclusions are irregular, their fractal dimensions are large.%通过对304/304L不锈钢轧材中大型夹杂物和铸锭中显微夹杂物的图像进行处理,得到夹杂物边界的二值图像.采用计盒维数法对夹杂物轮廓的分形维数进行计算与分析,算法利用MATLAB编程实现.结果表明,夹杂物的分形维数与其组成和熔点密切相关,低熔点的Al2O3-SiO2-CaO系复合夹杂的形貌多为球形或类球形,其分形维数较小;高熔点的Al2O3夹杂物与SiQ2夹杂物的形貌多为不规则形,其分形维数较大.

  3. 304奥氏体不锈钢铸锭中非金属夹杂物研究%Research on Non-metallic Inclusions in 304 Austenitic Stainless Steel Ingot

    Institute of Scientific and Technical Information of China (English)

    张雅丽; 王建军; 罗林根; 郭上型; 孔辉; 周俐

    2011-01-01

    The type and the amount of the non-metallic inclusions in 304 stainless steel ingot were investigated, with a tracer used to find out the origin of inclusion. The results show that most of the micro inclusions are Al2Or-SiO2-CaO system inclusions, the micro inclusions (<5 urn) coexit amount of MgO-Al2O3 spinel inclusions;the macro inclusion is main to have two types of compound admixture, respectively is the type of Al2O3-SiOr-CaO.the type of Al2O3-SiO2; one of the main source of the non-matallic inclusions is the slag for the refractory corrosion in the molten steel during tapping; ladle lining affects slightly.%研究304不锈钢铸锭中非金属夹杂物的类型和数量,通过示踪剂分析不锈钢中夹杂物的来源.结果表明:不锈钢铸锭中显微夹杂物主要是以Al2O3-SiO2-CaO系硅酸盐夹杂为主,粒度<5μm的显微夹杂物中同时存在大量的镁铝尖晶石夹杂;大型夹杂物主要有两类复合夹杂物Al2O3-SiO2-CaO系夹杂、Al2O3-SiO2系夹杂;汤道耐火材料的侵蚀是夹杂物主要来源之一,钢包耐火材料对夹杂生成的影响微弱.

  4. 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...

  5. 有机无机复混钾肥钾素表观释放特征及对烤烟产质量的影响%The K Apparent Release Characteristics of Organic-inorganic Compound Potash Fertilizers and Its Effect on Yield and Quality of Flue-cured Tobacco

    Institute of Scientific and Technical Information of China (English)

    余垚颖; 蒋长春; 顾会战; 王勇; 郭应菊; 喻晓; 王明富

    2016-01-01

    In order to solve the supply of K at 75 days after transplanting and increase the content of K in tobacco leaves, pot and field experiments were carried out to study the effects of the organic inorganic mixed fertilizers on the K apparent release characteristics and the effects of different application methods on yield and quality of tobacco leaves, as well as the content of total K and sensory quality. The results showed that 4 kinds of organic inorganic mixed potassium fertilizers of different organic matter content could slow down the apparent release rate of K, with the treatment group of organic matter content 18%, K2O content 24% had the best effect. Field experiments were carried out in 3 regions to verify the 30% organic inorganic mixed potassium fertilizer and screened method. The results showed that: the treatment group was significantly better than control in K content of tobacco leaf, yield, output value and sensory quality. K content of tobacco increased by 11.43%-25.87% in the three locations. The 30% organic inorganic mixed fertilizer could effectively slow down K release, significantly increase K content and improve inherent quality of tobacco Leaf.%为改善烟株移栽75 d后的钾素供应,提高中上部烟叶的含钾量,采用盆栽和大田相结合的方式,研究有机无机复混钾肥的钾素表观释放特征及不同施用方式对烟叶产质量、钾素含量及感观质量的影响.结果表明,4种不同有机质含量的有机无机复混钾肥均能改善钾素释放动态,提高烟株生育后期的钾素供应,其中以有机质含量18%,K2O含量24%处理最为理想;对研制的30%有机无机复混钾肥及筛选的施肥方法在3个地区进行同田对比试验表明,处理组在烟叶含钾量、产量、产值及感观质量上均要显著好于对照组,3个地区烟叶含钾量增幅为11.43%~25.87%.30%有机无机复混钾肥能有效减缓钾素释放,显著提高烟叶含钾量,明显改善内在品质.

  6. Highly Efficient Red-Light Emission in An Organic-Inorganic Hybrid Ferroelectric: (Pyrrolidinium)MnCl₃.

    Science.gov (United States)

    Zhang, Yi; Liao, Wei-Qiang; Fu, Da-Wei; Ye, Heng-Yun; Chen, Zhong-Ning; Xiong, Ren-Gen

    2015-04-22

    Luminescence of ferroelectric materials is one important property for technological applications, such as low-energy electron excitation. However, the vast majority of doped inorganic ferroelectric materials have low luminescent efficiency. The past decade has envisaged much progress in the design of both ferroelectric and luminescent organic-inorganic hybrid complexes for optoelectronic applications. The combination of ferroelectricity and luminescence within organic-inorganic hybrids would lead to a new type of luminescent ferroelectric multifunctional materials. We herein report a hybrid molecular ferroelectric, (pyrrolidinium)MnCl3, which exhibits excellent ferroelectricity with a saturation polarization of 5.5 μC/cm(2) as well as intense red luminescence with high quantum yield of 56% under a UV excitation. This finding may extend the application of organic-inorganic hybrid compounds to the field of ferroelectric luminescence and/or multifunctional devices.

  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. Soil Inorganic Nitrogen Cycling during Successional Change in a Northern Temperate Forest

    Science.gov (United States)

    Nave, L. E.; Sparks, J. P.; Le Moine, J.; Hardiman, B. S.; Nadelhoffer, K. J.; Strahm, B. D.; Curtis, P.

    2012-12-01

    Transformations and fluxes of inorganic nitrogen (N) compounds in forest soils are the basis for major biogeochemical functions. Inorganic N fluxes contribute significantly to plant and microbial N nutrition, mediate the exchange of reactive, gas-phase N between the biosphere and atmosphere, and are coupled via hydrologic linkages to N cycling in surface and groundwater. However, soil inorganic N cycling may change during forest succession due to shifts in tree species composition, ecosystem N capital and distribution, or other drivers. Within the framework of a paired-ecosystem, experimentally accelerated successional advancement, we synthesized comprehensive measurements of soil and soil surface inorganic N fluxes to: a) quantify changes in, and interactions between, the component processes of the N cycle that mediate forest biogeochemical functions, and b) understand how these processes and associated biogeochemical functions change during forest succession. We hypothesized that a sudden decline in plant N uptake during the mortality event that accelerated ongoing succession would significantly increase NH4+ availability, prompting fundamental changes to the N cycle including the initiation of significant nitrification and increased exports of NO3- derived compounds in gas phase and soil solution. We found that in surface soils (top 20 cm), levels of seasonally integrated, ion-exchange NH4+ and NO3- availability increased with decreasing fine root biomass (regression, Pstructural drivers of N cycling that are undergoing incipient successional changes, and b) recent and continued successional advancement has shifted the N cycling economy of this ecosystem towards greater importance of NO3-.

  10. Materials Chemistry and Performance of Silicone-Based Replicating Compounds.

    Energy Technology Data Exchange (ETDEWEB)

    Brumbach, Michael T.; Mirabal, Alex James; Kalan, Michael; Trujillo, Ana B; Hale, Kevin

    2014-11-01

    Replicating compounds are used to cast reproductions of surface features on a variety of materials. Replicas allow for quantitative measurements and recordkeeping on parts that may otherwise be difficult to measure or maintain. In this study, the chemistry and replicating capability of several replicating compounds was investigated. Additionally, the residue remaining on material surfaces upon removal of replicas was quantified. Cleaning practices were tested for several different replicating compounds. For all replicating compounds investigated, a thin silicone residue was left by the replica. For some compounds, additional inorganic species could be identified in the residue. Simple solvent cleaning could remove some residue.

  11. In vitro cytogenetic testing of an organoselenium compound and its sulfur analogue in cultured rat bone marrow cells

    Directory of Open Access Journals (Sweden)

    Jacob Jacob H

    2004-03-01

    Full Text Available Abstract Background Selenium (Se is a non-metal element, occurring in varying degrees in the environment and it has been found to be a component of several enzymes. Different selenium compounds have been associated with carcinogenicity, toxicity, modification of metal toxicity and prevention of cancer. Organoselenium compounds had substantially greater bioavailability and less toxicity than that of inorganic selenium. From a chemical point of view, Se resembles sulfur (S in many of its properties, thus, Se and S may be considered to be isosteric. The ability of a synthetic organoselenium compound; cyclopenta-dienyldicarbonyl ironselenoterephthalic acid (CSe and its sulfur analogue (CS in the range of 10-8 to 10-5 M, to induce sister-chormatid exchanges (SCE and alter cell division expressed as mitotic index (MI as well as cell survival has been investigated. Methods Rat bone marrow cells were cultured in the presence of CSe and CS in the range of 10-8 to 10-5 M with a total exposure time of 4, 16 or 28 h at 37°C. Fluorescence-plus-Giemsa (FPG technique was used to visualize chromosomes for SCE analysis and MI determination. Trypan blue exclusion technique was used to determine cell viability. Results At the three exposure times, cell survival progressively decreased with increasing concentration, but the effect of either chemical was not significant (ANOVA; P -5 M when either chemical was applied for 16 or 28 h. Furthermore, the mean SCE increased with longer exposure times and, in general, CSe had slightly greater effect on cell survival and caused higher frequencies of SCE than CS. The exception was the 10-8 M treatment. However, both CSe and CS failed to induce 2-fold SCE as that of the negative control and therefore they are not considered as mutagens. Conclusion Both CSe and CS in the range of 10-8 to 10-5 M could not double the SCE rate of the negative control and therefore not considered as mutagens at these experimental conditions.

  12. 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,…

  13. 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,…

  14. Multipurpose Compound

    Science.gov (United States)

    1983-01-01

    Specially formulated derivatives of an unusual basic compound known as Alcide may be the answer to effective treatment and prevention of the disease bovine mastitis, a bacterial inflammation of a cow's mammary gland that results in loss of milk production and in extreme cases, death. Manufactured by Alcide Corporation the Alcide compound has killed all tested bacteria, virus and fungi, shortly after contact, with minimal toxic effects on humans or animals. Alcide Corporation credits the existence of the mastitis treatment/prevention products to assistance provided the company by NERAC, Inc.

  15. 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.

  16. Imaging of metals, metalloids, and non-metals by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) in biological tissues.

    Science.gov (United States)

    Becker, J Sabine; Becker, J Susanne

    2010-01-01

    The determination of the localization and distribution of essential and beneficial metals (e.g., Cu, Fe, Zn, Mn, Co, Ti, Al, Ca, K, Na, Cr and others), toxic metals (like Cd, Pb, Hg, U), metalloids (e.g., As, Se, Sb), and non-metals (such as C, S, P, Cl, I) in biological tissues is a challenging task for life science studies. Over the past few years, the development and application of mass spectrometric imaging (MSI) techniques for elements has been rapidly growing in the life sciences in order to investigate the uptake and the transport of both essential and toxic metals in plant and animal sections. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) is a very sensitive and efficient trace, surface, and isotopic analytical technique for biological samples. LA-ICP-MS is increasingly utilized as an elemental mass spectrometric technique using double-focusing sector field (LA-ICP-SFMS) or quadrupole mass spectrometers (LA-ICP-QMS) to produce images of detailed regionally specific element distributions in thin biological tissue sections. Nowadays, MSI studies focus on brain research for studying neurodegenerative diseases such as Alzheimer's or Parkinson's, stroke, or tumor growth, or for the imaging of cancer biomarkers in tissue sections.The combination of the mass spectrometry imaging of metals by LA-ICP-MS with proteomics using biomolecular mass spectrometry (such as MALDI-MS or ESI-MS) to identify metal-containing proteins has become an important strategy in the life sciences. Besides the quantitative imaging of metals, non-metals and metalloids in biological tissues, LA-ICP-MS has been utilized for imaging metal-containing proteins in a 2D gel after electrophoretic separation of proteins. Recent progress in applying LA-ICP-MS in life science studies will be reviewed including the imaging of thin slices of biological tissue and applications in proteome analysis in combination with MALDI/ESI-MS to analyze metal-containing proteins.

  17. Photocatalytic oxidation of organic compounds on Mars

    Science.gov (United States)

    Chun, S. F. S.; Pang, K. D.; Cutts, J. A.; Ajello, J. M.

    1978-01-01

    Ultraviolet-stimulated catalytic oxidation is proposed as a mechanism for the destruction of organic compounds on Mars. The process involves the presence of gaseous oxygen, UV radiation, and a catalyst (titanium dioxide), and all three of these have been found to be present in the Martian environment. Therefore it seems plausible that UV-stimulated oxidation of organics is responsible for degrading organic molecules into inorganic end products.

  18. The Surface Morphology and Optical Properties of Refined Glasses with Inorganic Nano-molecules

    Science.gov (United States)

    Drajewicz, Marcin; Pytel, Maciej; Rokicki, Paweł; Góral, Marek

    2015-05-01

    New refining technology of soda-calcium-silicon glass surfaces with inorganic compounds nano-molecules has been presented in the study. In order to determine modification of the glass surface SEM observation and EDX analysis have been carried out. The UV-VIS, photo-elasticity and ellipsometry examinations were carried out on glass samples. The results of investigations that have been conducted show that refining process of the glass surface by use of nanopowder inorganic compounds deposited electrostatically on glass surface provides forming of very thin (about 50 nm) surface layers [1]. This method of surface modification improves physical and chemical glass properties. In this paper results of microhardness test of refined glass were also presented.

  19. Electric-Magneto-Optical Kerr Effect in a Hybrid Organic-Inorganic Perovskite.

    Science.gov (United States)

    Fan, Feng-Ren; Wu, Hua; Nabok, Dmitrii; Hu, Shunbo; Ren, Wei; Draxl, Claudia; Stroppa, Alessandro

    2017-09-20

    Hybrid organic-inorganic compounds attract a lot of interest for their flexible structures and multifunctional properties. For example, they can have coexisting magnetism and ferroelectricity whose possible coupling gives rise to magnetoelectricity. Here using first-principles computations, we show that, in a perovskite metal-organic framework (MOF), the magnetic and electric orders are further coupled to optical excitations, leading to an Electric tuning of the Magneto-Optical Kerr effect (EMOKE). Moreover, the Kerr angle can be switched by reversal of both ferroelectric and magnetic polarization only. The interplay between the Kerr angle and the organic-inorganic components of MOFs offers surprising unprecedented tools for engineering MOKE in complex compounds. Note that this work may be relevant to acentric magnetic systems in general, e.g., multiferroics.

  20. SYNTHESIS AND BIOTECHNOLOGICAL APPLICATIONS OF VINYL POLYMER-INORGANIC HYBRID AND MESOPOROUS MATERIALS

    Institute of Scientific and Technical Information of China (English)

    Yen Wei; Kun-yuan Qiu

    2000-01-01

    We describe the sol-gel synthesis of a new family of organic-inorganic hybrid materials, in which various vinyl polymers are covalently bonded to and uniformly distributed in inorganic oxide matrices. The materials can be tailored to have both good toughness and hardness while maintaining excellent optical transparency. Doping the sol-gel metal oxides with optically active compounds such as D-glucose results in new optical rotatory composite materials. Removal of the dopant compounds from the composites affords mesoporous oxide materials, which represents a new, nonsurfactant-templated route to mesoporous molecular sieves. We have successfully immobilized a series of enzymes and other bioactive agents in mesoporous materials. Catalytical activities of the enzyme encapsulated in mesoporous materials were found to be much higher than those encapsulated in microporous materials.

  1. 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.

  2. 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.

  3. 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.

  4. Organic and inorganic decomposition products from the thermal desorption of atmospheric particles

    OpenAIRE

    Williams, Brent J.; Zhang, Yaping; Zuo, Xiaochen; Martinez, Raul E.; Walker, Michael J.; Kreisberg, Nathan M.; Goldstein, Allen H.; Docherty, Kenneth S.; Jimenez, Jose L.

    2016-01-01

    Atmospheric aerosol composition is often analyzed using thermal desorption techniques to evaporate samples and deliver organic or inorganic molecules to various designs of detectors for identification and quantification. The organic aerosol (OA) fraction is composed of thousands of individual compounds, some with nitrogen- and sulfur-containing functionality and, often contains oligomeric material, much of which may be susceptible to decomposition upon heating. Here we analy...

  5. Organic and inorganic decomposition products from the thermal desorption of atmospheric particles

    OpenAIRE

    B. J. Williams; Y. Zhang; X. Zuo; R. E. Martinez; Walker, M. J.; N. M. Kreisberg; Goldstein, A. H.; K. S. Docherty; Jimenez, J.L.

    2015-01-01

    Atmospheric aerosol composition is often analyzed using thermal desorption techniques to evaporate samples and deliver organic or inorganic molecules to various designs of detectors for identification and quantification. The organic aerosol (OA) fraction is composed of thousands of individual compounds, some with nitrogen- and sulfur-containing functionality, and often contains oligomeric material, much of which may be susceptible to decomposition upon heating. Here we analy...

  6. Partition of biocides between water and inorganic phases of renders with organic binder

    DEFF Research Database (Denmark)

    Urbanczyk, Michal M; Bollmann, Ulla E; Bester, Kai

    2016-01-01

    , the partition of biocides between water and inorganic phases of render with organic binder was investigated. The partition constants of carbendazim, diuron, iodocarb, isoproturon, cybutryn (irgarol), octylisothiazolinone, terbutryn, and tebuconazole towards minerals typically used in renders, e.g. barite...... with render-water distribution constants of two artificially made renders showed that the distribution constants can be estimated based on partition constants of compounds for individual components of the render....

  7. 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.

  8. Potential of laser ablation and laser desorption mass spectrometry to characterize organic and inorganic environmental pollutants on dust particles.

    NARCIS (Netherlands)

    Carre, V.; Aubriet, F.; Scheepers, P.T.J.; Krier, G.; Muller, J.F.

    2005-01-01

    Stainless steel factories are known to release particles into the atmosphere. Such particulate matter contains significant amounts of heavy metals or toxic inorganic compounds and organic pollutants such as, for example, Cr(VI) and polycyclic aromatic hydrocarbons (PAHs). The investigation of Cr(VI)

  9. Potential of laser ablation and laser desorption mass spectrometry to characterize organic and inorganic environmental pollutants on dust particles.

    NARCIS (Netherlands)

    Carre, V.; Aubriet, F.; Scheepers, P.T.J.; Krier, G.; Muller, J.F.

    2005-01-01

    Stainless steel factories are known to release particles into the atmosphere. Such particulate matter contains significant amounts of heavy metals or toxic inorganic compounds and organic pollutants such as, for example, Cr(VI) and polycyclic aromatic hydrocarbons (PAHs). The investigation of Cr(VI)

  10. Artificial neural networks to evaluate organic and inorganic contamination in agricultural soils.

    Science.gov (United States)

    Bonelli, Maria Grazia; Ferrini, Mauro; Manni, Andrea

    2017-11-01

    The assessment of organic and inorganic contaminants in agricultural soils is a difficult challenge due to the large-scale dimensions of the areas under investigation and the great number of samples needed for analysis. On-site screening techniques, such as Field Portable X-ray Fluorescence (FPXRF) spectrometry, can be used for inorganic compounds, such as heavy metals. This method is not destructive and allows a rapid qualitative characterization, identifying hot spots from where to collect soil samples for analysis by traditional laboratory techniques. Recently, fast methods such as immuno-assays for the determination of organic compounds, such as dioxins, furans and PCBs, have been employed, but several limitations compromise their performance. The aim of the present study was to find a method able to screen contaminants in agricultural soil, using FPXRF spectrometry for metals and a statistical procedure, such as the Artificial Neural Networks technique, to estimate unknown concentrations of organic compounds based on statistical relationships between the organic and inorganic pollutants. Copyright © 2017 Elsevier Ltd. All rights reserved.

  11. Survey of inorganic arsenic in marine animals and marine certified reference materials by anion exchange high-performance liquid chromatography-inductively coupled plasma mass spectrometry

    DEFF Research Database (Denmark)

    Sloth, Jens Jørgen; Larsen, Erik Huusfeldt; Julshamn, Kåre

    2005-01-01

    A method for the determination of inorganic arsenic in seafood samples using high-performance liquid chromatography-inductively coupled plasma mass spectrometry is described. The principle of the method relied on microwave-assisted alkaline dissolution of the sample, which at the same time oxidized...... arsenite [As(Ill)] to arsenate [As(V)], whereby inorganic arsenic could be determined as the single species As(V). Anion exchange chromatography using isocratic elution with aqueous ammonium carbonate as the mobile phase was used for the separation of As(V) from other coextracted organoarsenic compounds......, including arsenobetaine. The stability of organoarsenic compounds during the sample pretreatment was investigated, and no degradation/conversion to inorganic arsenic was detected. The method was employed for the determination of inorganic arsenic in a variety of seafood samples including fish, crustaceans...

  12. Intermetallic Compounds

    Science.gov (United States)

    Takagiwa, Y.; Matsuura, Y.; Kimura, K.

    2014-06-01

    We have focused on the binary narrow-bandgap intermetallic compounds FeGa3 and RuGa3 as thermoelectric materials. Their crystal structure is FeGa3-type (tetragonal, P42/ mnm) with 16 atoms per unit cell. Despite their simple crystal structure, their room temperature thermal conductivity is in the range 4-5-W-m-1-K-1. Both compounds have narrow-bandgaps of approximately 0.3-eV near the Fermi level. Because their Seebeck coefficients are quite large negative values in the range 350-FeGa3 and RuGa3 as n and p-type materials. The dimensionless figure of merit, ZT, was significantly improved by substitution of Sn for Ga in FeGa3 (electron-doping) and by substitution of Zn for Ga in RuGa3 (hole-doping), mainly as a result of optimization of the electronic part, S 2 σ.

  13. Organic Compounds

    Science.gov (United States)

    Shankland, Kenneth

    For many years, powder X-ray diffraction was used primarily as a fingerprinting method for phase identification in the context of molecular organic materials. In the early 1990s, with only a few notable exceptions, structures of even moderate complexity were not solvable from PXRD data alone. Global optimisation methods and highly-modified direct methods have transformed this situation by specifically exploiting some well-known properties of molecular compounds. This chapter will consider some of these properties.

  14. Compound odontoma

    Directory of Open Access Journals (Sweden)

    Monica Yadav

    2012-01-01

    Full Text Available Odontomas have been extensively reported in the dental literature, and the term refers to tumors of odontogenic origin. Though the exact etiology is still unknown, the postulated causes include: local trauma, infection, inheritance and genetic mutation. The majority of the lesions are asymptomatic; however, may be accompanied with pain and swelling as secondary complaints in some cases. Here, we report a case of a compound odontome in a 14 year old patient.

  15. Measured and modeled humidification factors of fresh smoke particles from biomass burning: role of inorganic constituents

    Directory of Open Access Journals (Sweden)

    J. L. Hand

    2010-07-01

    Full Text Available During the 2006 FLAME study (Fire Laboratory at Missoula Experiment, laboratory burns of biomass fuels were performed to investigate the physico-chemical, optical, and hygroscopic properties of fresh biomass smoke. As part of the experiment, two nephelometers simultaneously measured dry and humidified light scattering coefficients (bsp(dry and bsp(RH, respectively in order to explore the role of relative humidity (RH on the optical properties of biomass smoke aerosols. Results from burns of several biomass fuels from the west and southeast United States showed large variability in the humidification factor (f(RH=bsp(RH/bsp(dry. Values of f(RH at RH=80–85% ranged from 0.99 to 1.81 depending on fuel type. We incorporated measured chemical composition and size distribution data to model the smoke hygroscopic growth to investigate the role of inorganic compounds on water uptake for these aerosols. By assuming only inorganic constituents were hygroscopic, we were able to model the water uptake within experimental uncertainty, suggesting that inorganic species were responsible for most of the hygroscopic growth. In addition, humidification factors at 80–85% RH increased for smoke with increasing inorganic salt to carbon ratios. Particle morphology as observed from scanning electron microscopy revealed that samples of hygroscopic particles contained soot chains either internally or externally mixed with inorganic potassium salts, while samples of weak to non-hygroscopic particles were dominated by soot and organic constituents. This study provides further understanding of the compounds responsible for water uptake by young biomass smoke, and is important for accurately assessing the role of smoke in climate change studies and visibility regulatory efforts.

  16. Measured and modeled humidification factors of fresh smoke particles from biomass burning: role of inorganic constituents

    Directory of Open Access Journals (Sweden)

    J. L. Hand

    2010-02-01

    Full Text Available During the 2006 FLAME study (Fire Laboratory at Missoula Experiment, laboratory burns of biomass fuels were performed to investigate the physico-chemical, optical, and hygroscopic properties of fresh biomass smoke. As part of the experiment, two nephelometers simultaneously measured dry and humidified light scattering coefficients (bsp(dry and bsp(RH, respectively in order to explore the role of relative humidity (RH on the optical properties of biomass smoke aerosols. Results from burns of several biomass fuels showed large variability in the humidification factor (f(RH=bsp(RH/bsp(dry. Values of f(RH at RH=85–90% ranged from 1.02 to 2.15 depending on fuel type. We incorporated measured chemical composition and size distribution data to model the smoke hygroscopic growth to investigate the role of inorganic and organic compounds on water uptake for these aerosols. By assuming only inorganic constituents were hygroscopic, we were able to model the water uptake within experimental uncertainty, suggesting that inorganic species were responsible for most of the hygroscopic growth. In addition, humidification factors at 85–90% RH increased for smoke with increasing inorganic salt to carbon ratios. Particle morphology as observed from scanning electron microscopy revealed that samples of hygroscopic particles contained soot chains either internally or externally mixed with inorganic potassium salts, while samples of weak to non-hygroscopic particles were dominated by soot and organic constituents. This study provides further understanding of the compounds responsible for water uptake by young biomass smoke, and is important for accurately assessing the role of smoke in climate change studies and visibility regulatory efforts.

  17. 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...

  18. Electrode reactions and electroanalysis of organomercury compounds

    Energy Technology Data Exchange (ETDEWEB)

    Kurmaz, Vladimir A [Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka, Moscow Region (Russian Federation); Gul' tyai, Vadim P [N.D.Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow (Russian Federation)

    2010-06-09

    Characteristic features of mechanisms and kinetics of electrode reactions of organomercury compounds (symmetrical, non-symmetrical) and organomercury salts on a mercury electrode are analyzed. Attention is focused on the effect of coordination, adsorption and the nature and properties of intermediates on these processes as well as on the formation of organomercury derivatives in the adsorption of organic and hetero-organic compounds on a mercury electrode. The kinetics of heterogeneous chemical equilibrium {sup o}rganic calomel{sup -}symmetrical organomercury compound in the adsorption layer and the relative stability of intermediates in the one-electron reduction of organomercury salts are discussed as well as the electrolytic hydrogen evolution catalyzed by organomercury intermediates. The problems of combined and separate electrochemical quantitation of organic and inorganic mercury compounds in natural objects are considered.

  19. Non-fibrous inorganic particles in human bronchoalveolar lavage fluids.

    Science.gov (United States)

    Dumortier, P; De Vuyst, P; Yernault, J C

    1989-12-01

    Bronchoalveolar lavage (BAL) is a simple and non-invasive sampling technique of the deep lung. Analytical electron microscopy was used for the identification and quantification of non-fibrous inorganic particles recovered in BAL fluid samples from 51 subjects with various occupational exposures (silica, silicates, metals and alloys, metallic oxides, precious and hard metals, abrasives). Around 4750 particles were analysed. More than sixty different compounds were identified, among which silica, kaolinite, illite, mica, Fe oxides and hydroxides, appeared to be ubiquitous. Feldspar, talc, chlorite, Al oxide, Ti oxide, tungsten carbide, stainless steel, carbonaceous compounds and flyash were also frequently encountered. From 1 to 21 compounds were identified in each sample. Repeated BAL samples obtained for 2 subjects did not show significant differences. Particles characteristic of the occupational exposure were found in BAL up to 21 years after cessation. BAL content can also reflect mixed occupational exposures. Absolute particle concentrations measured in twelve samples ranged between 0.1 and 9.9 x 10(6) particles/ml BAL fluid and mean particle diameter ranged between 0.5 and 1.2 microns. Mineralogical analysis of non-fibrous particles in BAL can be a useful tool to investigate occupational exposures. It allows, in most cases, a better characterization of the exposure than medical questioning. It may be helpful in identifying pathogenic particles, however it must be kept in mind that a positive result is only a proof of exposure and never a proof of disease. The main limitations of this technique are difficulties in sampling severely diseased subjects and inaccuracy in detecting easily soluble compounds and particles with a high rate of alveolar clearance.

  20. 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.

  1. 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)

  2. 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...

  3. 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)

  4. 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.

  5. 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...

  6. Influence of Organic and Inorganic Sources of Fertilizer on Growth ...

    African Journals Online (AJOL)

    Influence of Organic and Inorganic Sources of Fertilizer on Growth and Leaf Yield of ... the effect of Tithonia diversifolia, farmyard manure and inorganic sources of ... Leaf yield was assessed by both cumulative leaf weight per given plant and ...

  7. Inorganic Nitrogen Wet Deposition for the Conterminous United States, 1963

    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 1963. 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, 1961

    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 1961. The estimates were derived from inorganic nitrogen...

  10. 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...

  11. 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

  12. Analysis of industry development of building materials and ore mining and dressing of non-metallic minerals%2011年建材及非金属矿采选业行业发展分析

    Institute of Scientific and Technical Information of China (English)

    何军生

    2012-01-01

    In 2011, the growth of building materials production remained stable, industrial structure contiuned to optimise, economic porfits improved. In this paper, the author firstly discusses economic operation of building materials and ore mining and dressing of non-metallic minerals in 2011, to adjust the industrial structure of building materials and ore mining and dressing of non-metallic minerals to impove the quality of the economic operation, predicts the development trend of industry of building materials and ore mining and dressing of non-metallic minerals in 2012. At last, the author puts forward to policy suggestions which accelerate industry deleopment of the building materials and ore mining and dressing of non-metallic minerals%2011年建材工业生产增长速度保持平稳,产业结构继续优化,经济效益提高.本文首先讨论了2011年建材工业经济及非金属矿采选行业经济运行情况,做到调整建材及非金属矿选行业产业结构,提高经济运行质量,预测了2012年建材及非金属矿选行业未来发展趋势,最后提出促进建材及非金属矿选行业发展的政策建议.

  13. 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.

  14. Microstructure of organic–inorganic composite coatings studied by TEM and XANES

    Directory of Open Access Journals (Sweden)

    Etsuo Hamada, Masayasu Nagoshi, Kaoru Sato, Akira Matsuzaki, Takafumi Yamaji and Kotaro Kuroda

    2003-01-01

    Full Text Available Chromate coatings on Zn or Zn alloy coated steel sheets often include silica for the aim to improve corrosion resistance. In the case of dry-in-place chromate coatings containing acrylic resin (hereafter referred to as an organic–inorganic composite coating, an addition of silica, however, did not show an improvement in corrosion resistance. The microstructures of the organic–inorganic composite coatings were observed by transmission electron microscopy (TEM and the chemical states of Cr were investigated by the total electron yield X-ray absorption near edge structure (TEY-XANES method. TEM samples were successfully prepared by dry ultramicrotomy preventing water-soluble components in the coatings from dissolving out. TEY-XANES revealed the chemical states of components even in the organic matrix. Using these methods, it was found that the addition of silica changed just the morphology of the chromium compound in the organic–inorganic composite coating but not the chemical state of Cr. This is a reason for the addition of silica being not effective at improving corrosion resistance. The combination of dry ultramicrotomy-TEM and TEY-XANES spectroscopy was proven to be a powerful tool for characterizing organic–inorganic composite coatings.

  15. Stability of Sunscreens Containing CePO4: Proposal for a New Inorganic UV Filter

    Directory of Open Access Journals (Sweden)

    Vitor C. Seixas

    2014-07-01

    Full Text Available Inorganic UV filters have become attractive because of their role in protecting the skin from the damage caused by continuous exposure to the sun. However, their large refractive index and high photocatalytic activity have led to the development of alternative inorganic materials such as CePO4 for application as UV filters. This compound leaves a low amount of white residue on the skin and is highly stable. The aim of this study was to evaluate the physical and chemical stability of a cosmetic formulation containing ordinary organic UV filters combined with 5% CePO4, and, to compare it with other formulations containing the same vehicle with 5% TiO2 or ZnO as inorganic materials. The rheological behavior and chemical stability of the formulations containing these different UV filters were investigated. Results showed that the formulation containing CePO4 is a promising innovative UV filter due to its low interaction with organic filters, which culminates in longer shelf life when compared with traditional formulations containing ZnO or TiO2 filters. Moreover, the recognized ability of CePO4 to leave a low amount of white residue on the skin combined with great stability, suggests that CePO4 can be used as inorganic filter in high concentrations, affording formulations with high SPF values.

  16. Multidrug efflux transporters limit accumulation of inorganic, but not organic, mercury in sea urchin embryos.

    Science.gov (United States)

    Bosnjak, Ivana; Uhlinger, Kevin R; Heim, Wesley; Smital, Tvrtko; Franekić-Colić, Jasna; Coale, Kenneth; Epel, David; Hamdoun, Amro

    2009-11-01

    Mercuric compounds are persistent global pollutants that accumulate in marine organisms and in humans who consume them. While the chemical cycles and speciation of mercury in the oceans are relatively well described, the cellular mechanisms that govern which forms of mercury accumulate in cells and why they persist are less understood. In this study we examined the role of multidrug efflux transport in the differential accumulation of inorganic (HgCl(2)) and organic (CH(3)HgCl) mercury in sea urchin (Strongylocentrotus purpuratus) embryos. We found that inhibition of MRP/ABCC-type transporters increases intracellular accumulation of inorganic mercury but had no effect on accumulation of organic mercury. Similarly, pharmacological inhibition of metal conjugating enzymes by ligands GST/GSH significantly increases this antimitotic potency of inorganic mercury, but had no effect on the potency of organic mercury. Our results point to MRP-mediated elimination of inorganic mercury conjugates as a cellular basis for differences in the accumulation and potency of the two major forms of mercury found in marine environments.

  17. 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

  18. Construction of stable Ta3N5/g-C3N4 metal/non-metal nitride hybrids with enhanced visible-light photocatalysis

    Science.gov (United States)

    Jiang, Yinhua; Liu, Peipei; Chen, YeCheng; Zhou, Zhengzhong; Yang, Haijian; Hong, Yuanzhi; Li, Fan; Ni, Liang; Yan, Yongsheng; Gregory, Duncan H.

    2017-01-01

    In this paper, a novel Ta3N5/g-C3N4 metal/non-metal nitride hybrid was successfully synthesized by a facile impregnation method. The photocatalytic activity of Ta3N5/g-C3N4 hybrid nitrides was evaluated by the degradation of organic dye rhodamine B (RhB) under visible light irradiation, and the result indicated that all Ta3N5/g-C3N4 samples exhibited distinctly enhanced photocatalytic activities for the degradation of RhB than pure g-C3N4. The optimal Ta3N5/g-C3N4 composite sample, with Ta3N5 mass ratio of 2%, demonstrated the highest photocatalytic activity, and its degradation rate constant was 2.71 times as high as that of pure g-C3N4. The enhanced photocatalytic activity of this Ta3N5/g-C3N4 metal/metal-free nitride was predominantly attributed to the synergistic effect which increased visible-light absorption and facilitated the efficient separation of photoinduced electrons and holes. The Ta3N5/g-C3N4 hybrid nitride exhibited excellent photostability and reusability. The possible mechanism for improved photocatalytic performance was proposed. Overall, this work may provide a facile way to synthesize the highly efficient metal/metal-free hybrid nitride photocatalysts with promising applications in environmental purification and energy conversion.

  19. 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...

  20. Magnesium compounds

    Science.gov (United States)

    Kramer, D.A.

    2012-01-01

    Seawater and natural brines accounted for about 57 percent of magnesium compounds produced in the United States in 2011. Dead-burned magnesia was produced by Martin Marietta Magnesia Specialties LLC from well brines in Michigan. Caustic-calcined magnesia was recovered from seawater by Premier Magnesia LLC in Florida, from well brines in Michigan by Martin Marietta and from magnesite in Nevada by Premier Magnesia. Intrepid Potash Wendover LLC and Great Salt Lake Minerals Corp. recovered magnesium chloride brines from the Great Salt Lake in Utah. Magnesium hydroxide was produced from seawater by SPI Pharma Inc. in Delaware and Premier Magnesia in Florida, and by Martin Marietta from its brine operation in Michigan.

  1. The Inorganic Illustrator: A 3-D Graphical Supplement for Inorganic and Bioinorganic Chemistry Courses Distributed on CD-ROM

    Science.gov (United States)

    Childs, Scott L.; Hagen, Karl S.

    1996-10-01

    The visualization of molecular and solid state chemical structures in three dimensions is a particularly difficult problem for students to overcome when the primary means of communication is the two-dimensional world of textbooks, blackboards, and overhead projector screens. Recent editions of popular textbooks in organic, inorganic, and biochemistry have included stereoviews of molecules to aid the student, and stereoviews of crystal structures have been used in inorganic chemistry publications for many years. These are powerful aids for visualizing complex molecules, but with the exception of the biochemistry text mentioned above, they are limited to single, static images generally in black and white. Molecular model kits are routinely used very effectively in organic chemistry but their utility in inorganic chemistry is limited to all but the most simple molecules encountered. Now that personal computers are generally accessible and multimedia tools are starting to make an appearance in chemistry lecture halls (1), we can make our inorganic and bioinorganic chemistry and crystallography lectures come alive with the aid of the computer-based resources, which are the essence of this project. As part of this project we are accumulating a database of representative crystal structures of main group molecules, coordination complexes, organometallic compounds, small metalloproteins, bioinorganic model complexes, clusters, and solid state materials in Chem3D Plus format to be viewed with Chem3D Viewer, which is free software from Cambridge Scientific Computing. We are also generating a library of high-quality graphic images of these same molecules and structures using Cerius2 package from Molecular Simulations. These include polyhedral representations of clusters and solid state structures (see Fig. 1). Figure 1. Representation of the user interface: the title page and an example of polyhedral and ball-and-stick representation of an octanuclear iron-oxo cluster. The

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. Direct optical lithography of functional inorganic nanomaterials

    Science.gov (United States)

    Wang, Yuanyuan; Fedin, Igor; Zhang, Hao; Talapin, Dmitri V.

    2017-07-01

    Photolithography is an important manufacturing process that relies on using photoresists, typically polymer formulations, that change solubility when illuminated with ultraviolet light. Here, we introduce a general chemical approach for photoresist-free, direct optical lithography of functional inorganic nanomaterials. The patterned materials can be metals, semiconductors, oxides, magnetic, or rare earth compositions. No organic impurities are present in the patterned layers, which helps achieve good electronic and optical properties. The conductivity, carrier mobility, dielectric, and luminescence properties of optically patterned layers are on par with the properties of state-of-the-art solution-processed materials. The ability to directly pattern all-inorganic layers by using a light exposure dose comparable with that of organic photoresists provides an alternate route for thin-film device manufacturing.

  7. 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.

  8. The crystal chemistry of inorganic metal borohydrides and their relation to metal oxides.

    Science.gov (United States)

    Černý, Radovan; Schouwink, Pascal

    2015-12-01

    The crystal structures of inorganic homoleptic metal borohydrides are analysed with respect to their structural prototypes found amongst metal oxides in the inorganic databases such as Pearson's Crystal Data [Villars & Cenzual (2015). Pearson's Crystal Data. Crystal Structure Database for Inorganic Compounds, Release 2014/2015, ASM International, Materials Park, Ohio, USA]. The coordination polyhedra around the cations and the borohydride anion are determined, and constitute the basis of the structural systematics underlying metal borohydride chemistry in various frameworks and variants of ionic packing, including complex anions and the packing of neutral molecules in the crystal. Underlying nets are determined by topology analysis using the program TOPOS [Blatov (2006). IUCr CompComm. Newsl. 7, 4-38]. It is found that the Pauling rules for ionic crystals apply to all non-molecular borohydride crystal structures, and that the latter can often be derived by simple deformation of the close-packed anionic lattices c.c.p. and h.c.p., by partially removing anions and filling tetrahedral or octahedral sites. The deviation from an ideal close packing is facilitated in metal borohydrides with respect to the oxide due to geometrical and electronic considerations of the BH4(-) anion (tetrahedral shape, polarizability). This review on crystal chemistry of borohydrides and their similarity to oxides is a contribution which should serve materials engineers as a roadmap to design new materials, synthetic chemists in their search for promising compounds to be prepared, and materials scientists in understanding the properties of novel materials.

  9. 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

  10. 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...

  11. 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.

  12. 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.

  13. 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

    2017-02-15

    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.

  14. 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.

  15. Aqueous SARA ATRP using Inorganic Sulfites.

    Science.gov (United States)

    Abreu, Carlos M R; Fu, Liye; Carmali, Sheiliza; Serra, Arménio C; Matyjaszewski, Krzysztof; Coelho, Jorge F J

    2017-01-14

    Aqueous supplemental activator and reducing agent atom transfer radical polymerization (SARA ATRP) using inorganic sulfites was successfully carried out for the first time. Under optimized conditions, a well-controlled poly[oligo(ethylene oxide) methyl ether acrylate] (POEOA) was obtained with sulfites (e.g. Na2S2O4) were continuously fed into the reaction mixture. The mechanistic studies proved that these salts can activate alkyl halides directly and regenerate the activator complex. The effects of the feeding rate of the SARA agent (inorganic sulfites), ligand and its concentration, halide salt and its concentration, sulfite used, and copper concentration, were systematically studied to afford fast polymerizations rates while maintaining the control over polymerization. The kinetic data showed linear first-order kinetics, linear evolution of molecular weights with conversion, and polymers with narrow molecular weight distributions (Đ ~1.2) during polymerization even at relatively high monomer conversions (~80%). "One-pot" chain extension and "one-pot" block copolymerization experiments proved the high chain-end functionality. The polymerization could be directly regulated by starting or stopping the continuous feeding of the SARA agent. Under biologically relevant conditions, the aqueous SARA ATRP using inorganic sulfites was used to synthesize a well-defined protein-polymer hybrid by grafting of P(OEOA480) from BSA-O-[iBBr]30.

  16. 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.

  17. 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.

  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. 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.

  20. Optical Spectroscopy on the Spin-Peierls Compound CuGeO3

    NARCIS (Netherlands)

    van Loosdrecht, P.H.M.

    1998-01-01

    An overview is given of Raman and infrared spectroscopic studies of the inorganic spin-Peierls compound CuGeO3, with an emphasis on the magnetic fluctuations in the uniform, dimerized, and high field phases of this quasi one dimensional magneto-elastic compound.

  1. Composite block copolymer stabilized nanoparticles: simultaneous encapsulation of organic actives and inorganic nanostructures.

    Science.gov (United States)

    Gindy, Marian E; Panagiotopoulos, Athanassios Z; Prud'homme, Robert K

    2008-01-01

    We describe the preparation and characterization of hybrid block copolymer nanoparticles (NPs) for use as multimodal carriers for drugs and imaging agents. Stable, water-soluble, biocompatible poly(ethylene glycol)-block-poly(epsilon-caprolactone) NPs simultaneously co-encapsulating hydrophobic organic actives (beta-carotene) and inorganic imaging nanostructures (Au) are prepared using the flash nanoprecipitation process in a multi-inlet vortex mixer. These composite nanoparticles (CNPs) are produced with tunable sizes between 75 nm and 275 nm, narrow particle size distributions, high encapsulation efficiencies, specified component compositions, and long-term stability. The process is tunable and flexible because it relies on the control of mixing and aggregation timescales. It is anticipated that the technique can be applied to a variety of hydrophobic active compounds, fluorescent dyes, and inorganic nanostructures, yielding CNPs for combined therapy and multimodal imaging applications.

  2. Crystallinity of inorganic films grown by atomic layer deposition: Overview and general trends

    Science.gov (United States)

    Miikkulainen, Ville; Leskelä, Markku; Ritala, Mikko; Puurunen, Riikka L.

    2013-01-01

    Atomic layer deposition (ALD) is gaining attention as a thin film deposition method, uniquely suitable for depositing uniform and conformal films on complex three-dimensional topographies. The deposition of a film of a given material by ALD relies on the successive, separated, and self-terminating gas-solid reactions of typically two gaseous reactants. Hundreds of ALD chemistries have been found for depositing a variety of materials during the past decades, mostly for inorganic materials but lately also for organic and inorganic-organic hybrid compounds. One factor that often dictates the properties of ALD films in actual applications is the crystallinity of the grown film: Is the material amorphous or, if it is crystalline, which phase(s) is (are) present. In this thematic review, we first describe the basics of ALD, summarize the two-reactant ALD processes to grow inorganic materials developed to-date, updating the information of an earlier review on ALD [R. L. Puurunen, J. Appl. Phys. 97, 121301 (2005)], and give an overview of the status of processing ternary compounds by ALD. We then proceed to analyze the published experimental data for information on the crystallinity and phase of inorganic materials deposited by ALD from different reactants at different temperatures. The data are collected for films in their as-deposited state and tabulated for easy reference. Case studies are presented to illustrate the effect of different process parameters on crystallinity for representative materials: aluminium oxide, zirconium oxide, zinc oxide, titanium nitride, zinc zulfide, and ruthenium. Finally, we discuss the general trends in the development of film crystallinity as function of ALD process parameters. The authors hope that this review will help newcomers to ALD to familiarize themselves with the complex world of crystalline ALD films and, at the same time, serve for the expert as a handbook-type reference source on ALD processes and film crystallinity.

  3. Essential Trends in Inorganic Chemistry (by D. M. P. Mingos)

    Science.gov (United States)

    Phillips, Reviewed By David A.

    2000-05-01

    The author has chosen to present his material in a distinctly different fashion from that of most inorganic chemistry textbook writers. Most texts are a mix of theory chapters and descriptive chapters, with the latter focusing on specific groups of elements. However, after a chapter laying out the quantum mechanical basis of the periodic table, Mingos has elected to organize the remaining chapters around vertical, horizontal, and diagonal relationships, or on isoelectronic and isostoichiometric relationships. I think this approach has worked remarkably well. Chapters 2-5 contain a wealth of information accompanied by clear, coherent discussions of the underlying principles that account for the observed trends and anomalies. Every serious inorganic chemist should have a copy of this text on his or her bookshelf. Chapter 1 is the least effective part of the book. Some of the quantum number notation is incorrect (m rather than ml , s rather than ms), some of the language is imprecise, and there are a few clear-cut errors. There is a nice discussion comparing the rmax of 2s and 2p vs 3s and 3p orbitals. However, most readers would be better served by the treatments in advanced inorganic texts such as those by Shriver or Huheey. Chapter 2 addresses vertical trends in the main-group elements. After discussing the influence of atomic size on atomic properties, Mingos describes and explains the second-row anomalies and the reversals in trends resulting from the addition of 3d and 4f subshells. He goes on to account for a variety of trends in the physical and chemical properties of main-group elements and their compounds. The chapter ends with tables summarizing a wide variety of properties, providing a wealth of information I have not seen presented in such a compact format anywhere else. Chapter 3 addresses the horizontal trends and diagonal relationships of the main-group elements. Among the highlights are discussions of the role of exchange energies in determining

  4. 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

  5. Synthesis, Crystal Structure, and Characterization of a New Organic-Inorganic Hybrid Material:

    Directory of Open Access Journals (Sweden)

    Hela Ferjani

    2013-01-01

    Full Text Available The title compound is an organic-inorganic hybrid material. The single crystal X-ray diffraction investigation reveals that the studied compound crystallizes in the orthorhombic system, space group Pbca with the following lattice parameters:  (4 Å,  (3 Å,  (6 Å, and . The crystal lattice is composed of a discrete anion surrounded by piperazinium cations, chlorine anions, and water molecules. Complex hydrogen bonding interactions between , , organic cations, and water molecules form a three-dimensional network. Room temperature IR, Raman spectroscopy, and optical absorption of the title compound were recorded and analysed. The observed crystal morphology was compared to the simulated one using the Bravais-Friedel, Donnay-Harker model.

  6. 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.

  7. 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.

  8. 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

  9. Stable colloids in molten inorganic salts

    Energy Technology Data Exchange (ETDEWEB)

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

    2017-02-16

    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 processes1, 2, 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 other2. Electrostatic stabilization3, 4 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 chains2, 5. 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. Non-Metallic Biomaterials for Tooth Repair and Replacement. By Pekka Vallittu, Woodhead Publishing, 2013; 406 pages. Price £145.00/US$245.00/€175.00 ISBN 978-0-85709-244-1

    Directory of Open Access Journals (Sweden)

    Shu-Kun Lin

    2013-01-01

    Full Text Available 1. Discusses the properties of enamel and dentin and their role in adhesive dental restoration;2. Chapters also examine the wear properties of dental ceramics, glasses and bioactive glass ceramics for tooth repair and replacement;3. Dental composites and antibacterial restorative materials are also considered;4. Provides a concise overview of non-metallic biomaterials for dental clinicians, materials scientists and academic researchers alike.As the demand for healthy, attractive teeth increases, the methods and materials employed in restorative dentistry have become progressively more advanced. Non-metallic biomaterials for tooth repair and replacement focuses on the use of biomaterials for a range of applications in tooth repair and, in particular, dental restoration.

  11. Biochemical and medical importance of vanadium compounds.

    Science.gov (United States)

    Korbecki, Jan; Baranowska-Bosiacka, Irena; Gutowska, Izabela; Chlubek, Dariusz

    2012-01-01

    Vanadium belongs to the group of transition metals and is present in the air and soil contaminants in large urban agglomerations due to combustion of fossil fuels. It forms numerous inorganic compounds (vanadyl sulfate, sodium metavanadate, sodium orthovanadate, vanadium pentoxide) as well as complexes with organic compounds (BMOV, BEOV, METVAN). Depending on the research model, vanadium compounds exhibit antitumor or carcinogenic properties. Vanadium compounds generate ROS as a result of Fenton's reaction or of the reaction with atmospheric oxygen. They inactivate the Cdc25B(2) phosphatase and lead to degradation of Cdc25C, which induces G(2)/M phase arrest. In cells, vanadium compounds activate numerous signaling pathways and transcription factors, including PI3K-PKB/Akt-mTOR, NF-κB, MEK1/2-ERK, that cause cell survival or increased expression and release of VEGF. Vanadium compounds inhibit p53-dependent apoptosis and promote entry into the S phase of cells containing functional p53 protein. In addition, vanadium compounds, in particular organic derivatives, have insulin-mimetic and antidiabetic properties. Vanadium compounds lower blood glucose levels in animals and in clinical trials. They also inhibit the activity of protein tyrosine phosphatase 1B. By activating the PI3K-PKB/Akt pathway, vanadium compaunds increase the cellular uptake of glucose by the GLUT4 transporter. The PKB/Akt pathway is also used to inactivate glycogen synthase kinase-3. The impact of vanadium compounds on inflammatory reactions has not been fully studied. Vanadium pentoxide causes expression of COX-2 and the release of proinflammatory cytokines in a human lung fibroblast model. Other vanadium compounds activate NF-κB in macrophages by activating IKKβ.

  12. 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.

  13. 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

  14. Inorganic pyrophosphatases: structural diversity serving the function

    Science.gov (United States)

    Samygina, V. R.

    2016-05-01

    The review is devoted to ubiquitous enzymes, inorganic pyrophosphatases, which are essential in all living organisms. Despite the long history of investigations, these enzymes continue to attract interest. The review focuses on the three-dimensional structures of various representatives of this class of proteins. The structural diversity, the relationship between the structure and some properties of pyrophosphatases and various mechanisms of enzyme action related to the structural diversity of these enzymes are discussed. Interactions of pyrophosphatase with other proteins and possible practical applications are considered. The bibliography includes 56 references.

  15. 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.

  16. 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.

  17. 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.

  18. A new form of sulphur in coal: the discovery of an iron-sulphur coordination compound

    Energy Technology Data Exchange (ETDEWEB)

    Baruah, M.K.; Gogoi, P.C. [NNS College, Titabar (India). Dept. of Chemistry

    1998-07-01

    An iron-sulphur coordination compound in coal has been identified for the first time. Isolation of the compound from a high sulphur Indian coal sample was performed by extracting with tetrahydrofuran followed by methanol and ultimately separated by thin layer chromatography. Characterization of the compound by proton n.m.r., i.r., u.v. and chemical analyses of iron and sulphur reveals that iron atoms are bonded to thiophenic, aliphatic and inorganic sulphur atoms. Geochemical studies have revealed that the main sources of sulphur are inorganic and sulphur amino acids mostly cysteine, cystine and methionine. Identification of the coordination compound has confirmed the nature and occurrence of secondary sulphur in coal. This compound is considered to be a new form of sulphur because it is neither purely pyritic nor organic sulphur. The discovery of the Fe-S coordination compound is a great concern for the determination of the sulphur forms in coal. 50 refs., 3 figs.

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

    National Research Council Canada - National Science Library

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

    2017-01-01

    ...% 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.

  20. Electron–Rotor Interaction in Organic–Inorganic Lead Iodide Perovskites Discovered by Isotope Effects

    Energy Technology Data Exchange (ETDEWEB)

    Gong, Jue; Yang, Mengjin; Ma, Xiangchao; Schaller, Richard D.; Liu, Gang; Kong, Lingping; Yang, Ye; Beard, Matthew C.; Lesslie, Michael; Dai, Ying; Huang, Baibiao; Zhu, Kai; Xu, Tao

    2016-08-04

    We report on the carrier-rotor coupling effect in perovskite organic-inorganic hybrid lead iodide (CH3NH3PbI3) compounds discovered by isotope effects. Deuterated organic-inorganic perovskite compounds including CH3ND3PbI3, CD3NH3PbI3, and CD3ND3PbI3 were synthesized. Devices made from regular CH3NH3PbI3 and deuterated CH3ND3PbI3 exhibit comparable performance in band gap, current-voltage, carrier mobility, and power conversion efficiency. However, a time-resolved photoluminescence (TRPL) study reveals that CH3NH3PbI3 exhibits notably longer carrier lifetime than that of CH3ND3PbI3, in both thin-film and single-crystal formats. Furthermore, the comparison in carrier lifetime between CD3NH3PbI3 and CH3ND3PbI3 single crystals suggests that vibrational modes in methylammonium (MA+) have little impact on carrier lifetime. In contrast, the fully deuterated compound CD3ND3PbI3 reconfirmed the trend of decreasing carrier lifetime upon the increasing moment of inertia of cationic MA+. Polaron model elucidates the electron-rotor interaction.