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Atomic Ratio (atomic + ratio)
Selected AbstractsPreparation of shuttle-like Sb2S3 nanorod-bundles via a solvothermal approach under alkaline conditionCRYSTAL RESEARCH AND TECHNOLOGY, Issue 2 2010Ling Zhang Abstract Uniform shuttle-like Sb2S3 nanorod-bundles were synthesized via a polyvinylpyrrolidone (PVP) assisted solvothermal approach under alkaline condition, using antimony chloride (SbCl3) and thiourea (CH4N2S, Tu) as the starting materials in ethanol. The phase structure, composition and morphology of the product were characterized by means of X-ray diffraction (XRD), energy dispersive X-ray spectrometry (EDS), transmission electron microscopy (TEM), and high-resolution transmission electron microscopy (HRTEM). XRD and EDS results confirm that the synthesized Sb2S3 nanorod-bundles have an orthorhombic structure and an atomic ratio of 3:2 for S:Sb. TEM and HRTEM results show that the shuttle-like Sb2S3 bundles are composed of nanorods with a size distribution of 20-40 nm and growing along c-axis. Furthermore, experiments under different reaction conditions were carried out and the mechanism for the growth of nanorod-bundles was discussed (© 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Characterization of Lead Precipitate Following Uptake by Roots of Brassica junceaENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 11 2009Donald E. R. Meyers Abstract Seedlings of Brassica juncea (L.) Czern. were grown in solution culture for 14 d prior to exposure to Pb2+ at an activity of 31 ,M for 72 h. Electron-dense deposits found within the apoplast and symplast were analyzed using scanning transmission electron microscopy/energy dispersive spectroscopy to determine the chemical identity of the deposits and potential toxicity resistance mechanisms. Irrespective of the cellular compartment in which they were found, the deposits contained Pb, O, P, and Cl. For the extracellular deposits, the average Pb:P:O atomic ratio was 1:0.54:3.0, which together with the hexagonal crystal system suggests that Pb is present as chloropyromorphite (Pb5(PO4)3Cl). A weak Ca signal also was detected in approximately half of the spectra, possibly indicating the presence of small concentrations of phosphohedyphane (Pb3Ca2(PO4)3Cl). The evidence suggests that B. juncea resists Pb toxicity by storing precipitated Pb in the vacuole. [source] Sorption of humic acids and ,-endosulfan by clay mineralsENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 1 2006Sarunya Hengpraprom Abstract Sorption of ,-endosulfan by kaolinite and montmorillonite alone and in the presence of sorbed and dissolved humic acid (HA) was investigated (pH 8 and 25°C). Three types of HA, Elliot soil HA (EHA), Peat HA (PHA), and Summit Hill HA (SHHA), were used to represent typical humic substances found in soils. For sorption of HA by either mineral, Freundlich sorption coefficient (Kf) values appeared to decrease in the order of EHA > PHA > SHHA, which followed increasing polarity (expressed as the O/C atomic ratio) and decreasing percent-carbon content. For both clays, sorption of ,-endosulfan by the HA mineral complex was greater than for sorption by the clay alone. Sorption of ,-endosulfan by the HA mineral complexes followed the same order as the Kf of the HAs (EHA > PHA > SHHA). Based on the amount of HA adsorbed by each mineral, organic carbon partition coefficients (KOC) were determined for sorption of ,-endosulfan by two of the HA mineral complexes. The value of KOC for ,-endosulfan sorption was greater for kaolinite EHA than kaolinite SHHA. However, the opposite trend was found with the montmorillonite HA complexes. Montmorillonite appeared to sorb ,-endosulfan and/or HA with higher affinity than kaolinite, which likely is due to its 2:1 layer structure and higher surface area. Sorption of endosulfan diol, a hydrolysis product, by the minerals was much less than the parent pesticide. [source] Essential fatty acids and phosphorus in seston from lakes with contrasting terrestrial dissolved organic carbon contentFRESHWATER BIOLOGY, Issue 1 2007KELLY GUTSEIT Summary 1. It is often assumed that lakes highly influenced by terrestrial organic matter (TOM) have low zooplankton food quality because of elemental and/or biochemical deficiencies of the major particulate organic carbon pools. We used the biochemical [polyunsaturated fatty acids, especially eicosapentaenoic acid (EPA) , 20:5,3] and elemental (C : P ratio) composition of particulate matter (PM) as qualitative measures of potential zooplankton food in two categories of lakes of similar primary productivity, but with contrasting TOM influence (clear water versus humic lakes). 2. C : P ratios (atomic ratio) in PM were similar between lake categories and were above 400. The concentration (,g L,1) and relative content (,g mg C,1) of EPA, as well as the particulate organic carbon concentration, were higher in the humic lakes than in the clear-water lakes. 3. Our results show high fatty acid quality of PM in the humic lakes. The differences in the biochemical quality of the potential zooplankton food between lake categories can be attributed to the differences in their phytoplankton communities. 4. High biochemical quality of the food can result in high efficiency of energy transfer in the food chain and stimulate production at higher trophic levels, assuming that zooplankton are able to ingest and digest the resource available. [source] Hydrodenitrification with PdCu Catalysts: Catalyst Optimization by Experimental and Quantum Chemical ApproachesISRAEL JOURNAL OF CHEMISTRY, Issue 1 2006Irena Efremenko A continuous process for nitrate and nitrite abatement from drinking water by catalytic hydrogenation has been developed in our lab. We describe the experimental process development procedure, and support it with semiempirical quantum chemical methods. Comparisons of activated carbon (ACC) and silica glass fiber (GFC) cloths as supports for mono- and bimetallic Pd-Cu catalysts show the former to be 45-fold and 15-fold more active for nitrite and nitrate hydrogenation, respectively, than the latter. Catalysts prepared by selective deposition of Cu on Pd/ACC led to better activity for nitrate hydrogenation than catalysts prepared by co-impregnation or ion exchange methods. The optimal Cu:Pd atomic ratio was found to be 1:2. The computational results show the following: (i) The dispersion of Pd catalysts supported on ACC is much higher than that on GFC due to the larger surface area and higher density of adsorption sites, and that accounts for the higher activity of PdCu/ACC; (ii) Nanosized Pd particles supported on ACC have a semispherical shape and possess preferentially close-packed triangular surfaces, while Pd/GFC particles are extended in the direction parallel to the support surface and show both fcc (100) and (111) planes; (iii) The interaction of Cu atoms with both supports is stronger than that of Pd; adsorbed Cu atoms show a greater ability to form monometallic than bimetallic bonds and that should result in poor mixing of the metal upon co-impregnation, as was observed experimentally; (iv) Cu atoms in bimetallic PdCu particles admit a significant positive charge; the experimentally measured solubility of metal atoms correlates with their calculated charges. The best catalyst (2 wt%Pd-0.6 wt%Cu/ACC) was employed in a novel continuous flow reactor for nitrate hydrogenation in distilled and tap water. The advantages of the reactor investigated over a conventional packed bed reactor are discussed, suggesting a potential for further process intensification. [source] Fabrication of High-Purity Ti3SiC2 Powders by an In Situ Reaction of Polycarbosilane and Metal TitaniumJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 8 2010Jinshan Yang High-purity titanium silicon carbide powders were fabricated by an in situ reaction of polycarbosilane and metal titanium. The effects of the starting reagents and the pyrolysis temperature on the fabrication of high-purity Ti3SiC2 were studied. The results showed that high-purity Ti3SiC2 could be obtained when the atomic ratio of Ti:Si was 3:1.5 and the effect of the temperature of pyrolysis on the purity of the powders was insignificant. The atomic ratio of Ti:Si was calculated on the basis of the empirical formula of SiC2.5H7. [source] Deposition of Carbonated Hydroxyapatite (CO3HAp) on Poly(Methylmethacrylate) Surfaces by Decomposition of Calcium,EDTA ChelateJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2008Yusuf Yusufoglu Inspired from the nature, the development of organic,inorganic composites between polymers and hydroxyapatite (HAp) has been investigated extensively. In this study, bone-like apatite (carbonated hydroxyapatite, CO3HAp) was precipitated on poly(methylmethacrylate) (PMMA) films by the oxidative decomposition of Ca,EDTA (calcium,ethylenediamine tetraacetate) chelates. Corona-treated PMMA films were soaked in a Ca,EDTA,PO4,H2O2 solution and aged at 63°C and pH,9 for times ranging from 1 to 24 h. Apatite formed on PMMA films was characterized by X-ray diffraction, Fourier transform infrared (FTIR), Scanning electron microscope, energy-dipersive X-ray spectroscopy, and carbon analysis. The apatite was found to be CO3HAp with Ca/P atomic ratio ranging between 1.3 and 1.9. Elemental analyses indicated that the carbonate content of the apatite phase was around 6.5 wt% after 24 h of aging time. Lattice parameters were estimated using a Rietveld profile-analysis and found to be a=0.9438 nm and c=0.6901 nm. Furthermore, FTIR spectra indicated that the apatite deposited on PMMA was B-type CO3HAp, in which carbonate ions occupy the phosphate sites. In the first 3 h of aging, isolated rod-like HAp particles were observed. With time, the needle-like crystallites radiate from a nucleus to form double-spherulite shape particles. The crystallites grew into a continuous layer with a thickness of ,15 ,m after 24-h aging. The adhesive strength between the PMMA substrate and the apatite layer was determined to be around 1.7 MPa. [source] Design of Ceramic Materials for Chemical Sensors: Effect of SmFeO3 Processing on Surface and Electrical PropertiesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 2 2001Hiromichi Aono Perovskite-type SmFeO3 powders were prepared by the thermal decomposition of a heteronuclear complex, Sm(Fe(CN)6)·4H2O and by solid-state reaction between the corresponding single oxides, Sm2O3 and Fe2O3. The thermal decomposition behavior of the complex was studied by thermogravimetric analysis. X-ray diffractometry was used to investigate the structure of the products from the complex thermal decomposition and the formation of SmFeO3 from the oxide mixture. Powders prepared by both methods were used to deposit thick films onto alumina substrates with comb-type gold electrodes. The microstructure and chemical homogeneity of the film surfaces were investigated by scanning electron microscopy and Auger electron spectroscopy. Thick SmFeO3 single-phase films having a homogeneous elemental distribution on the surface were obtained when powder prepared by thermal decomposition of the complex was used for deposition, even when the powder was fired at low temperature (800°C). Surface chemical analysis was performed by X-ray photoelectron spectroscopy (XPS). The O 1s XPS line was deconvoluted into two peaks, attributed to adsorbed oxygen (Oad) and oxygen in the lattice (Olattice). Quantitative analysis showed that the surface coverage of iron, expressed as Fe/(Fe + Sm), was larger for the films prepared using the solid-state reacted powder. Although the Olattice/(Fe + Sm) atomic ratio was not influenced by the processing procedures (and, thus, by iron surface coverage), the amount of Oad decreased with increasing iron surface coverage. A model of the SmFeO3 surface was used to determine that the outermost layer of the perovskite-type SmFeO3 prepared from the complex consisted mainly of samarium ions that could each bond four adsorbed oxygen ions. A single oxygen ion could adsorb onto an iron ion, and therefore, the content of adsorbed oxygen was lower for the film prepared from the solid-state reacted powders, which showed larger iron surface coverage. Electrical conductance measurements, performed with increasing temperature in different gaseous environments, confirmed these findings. Higher conductances and lower activation energies were observed for the films with larger samarium surface coverage. [source] Zinc Vanadates in Vanadium Oxide-Doped Zinc Oxide VaristorsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 2 2001Huey-Hoon Hng Convergent-beam electron diffraction has been used to determine the space groups of ,- and ,-Zn3(VO4)2 particles in vanadium oxide-doped zinc oxide varistors. The crystal structure of ,-Zn3(VO4)2 has been determined to be monoclinic with space group P21 and lattice parameters of a= 9.80 Å, b= 8.34 Å, c= 10.27 Å, and ,= 115.8°, whereas that of ,-Zn3(VO4)2 is monoclinic with space group Cm and a= 10.40 Å, b= 8.59 Å, c= 9.44 Å, and ,= 98.8°. Energy-dispersive X-ray microanalysis of these two phases shows significant deviations from their expected stoichiometry. It is apparent that the ,-phase is, in fact, the metastable Zn4V2O9 phase, whereas the ,-phase either is a new oxide that consists of zinc, vanadium, and manganese or, more likely, is a zinc vanadate phase with a Zn:V atomic ratio of 1:1 that has the ability to go into solid solution with manganese. [source] Crystallization, microPIXE and preliminary crystallographic analysis of the complex between the third KH domain of hnRNP K and single-stranded DNAACTA CRYSTALLOGRAPHICA SECTION D, Issue 4 2004Paul H. Backe hnRNP K is one of the major proteins found in hnRNP particles which are ribonucleoprotein complexes containing proteins and pre-mRNA. hnRNP K contains hnRNP K homology (KH) domains which bind both CT-rich single-stranded DNA (ssDNA) and CU-rich ssRNA. Co-crystallization of the third KH domain of human hnRNP,K with a 15-mer ssDNA gave rod-shaped crystals belonging to the trigonal space group P3121 (unit-cell parameters a = 54.0, c = 149.7,Å) and diffracting to 2.4,Å resolution. MicroPIXE (proton-induced X-ray emission) experiments showed that the crystals contained the complex and that the phosphorus to sulfur atomic ratio was consistent with the asymmetric unit containing three KH3 domains per 15-mer ssDNA. This was confirmed by structure solution by molecular replacement. [source] Microporous Niobia,Silica Membrane with Very Low CO2 PermeabilityCHEMSUSCHEM CHEMISTRY AND SUSTAINABILITY, ENERGY & MATERIALS, Issue 5 2008Vittorio Boffa Dr. Abstract A sol,gel-derived microporous ceramic membrane with an exceptionally low permeability for CO2 from gaseous streams was developed and characterized. The sols were prepared from a mixture of niobium and silicon alkoxide precursors by acid-catalyzed synthesis. Microporous films were formed by coating asymmetric ,-alumina disks with the polymeric sol (Si/Nb=3:1), followed by calcination at 500,°C. The membrane consists of a 150-nm-thick layer with a Si/Nb atomic ratio of about 1.5. The single-gas permeance of small gas molecules such as H2, CH4, N2, and SF6 decreases steadily with kinetic diameter. Hydrogen, helium, and carbon dioxide follow an activated transport mechanism through the membrane. The permeance of CO2 in this membrane is much lower than that in pure silica, and its behavior deviates strongly from the general trend observed with the other gases. This is attributed to a relatively strong interaction between CO2 and adsorption sites in the niobia,silica membrane. [source] Geochemical Factors Controlling Radium Activity in a Sandstone AquiferGROUND WATER, Issue 4 2006Tim Grundl Geochemical processes behind the occurrence of radium activities in excess of the U.S. EPA's drinking water limit of 5 pCi/L combined radium were investigated in a regional sandstone aquifer located in southeastern Wisconsin. Geochemical speciation modeling (PHREEQC 2.7) combined with a detailed understanding of the regional flow system provided by recent flow modeling efforts was used to determine that radium coprecipitation into barite controls radium activity in the unconfined portion of the aquifer. As the aquifer transitions from unconfined to confined conditions, radium levels rise and the water becomes more sulfate rich yet the aquifer remains at saturation with barite throughout. Calculations based on published distribution coefficients and the observed Ra:Ba atomic ratios indicate that barite contains ,12 ,g/kg coprecipitated radium. Confined portions of the aquifer have high concentrations of sulfate, and barium concentrations become too low to be an effective control on radium activity. Additional, as yet undefined, controls on radium are operative in the downgradient, confined portion of the aquifer. [source] Study of the preparation and composition of the metallic function for the selective hydrogenation of CO2 to gasoline over bifunctional catalysts,JOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 2-3 2003Javier Ereña Abstract Bifunctional catalysts for the transformation of carbon dioxide and hydrogen into gasoline have been prepared by conventional and novel processes and characterized by measurement of BET surface area and volume and distribution of pores, and by X-ray diffraction, FTIR spectroscopy and X-ray fluorescence. The effects of the preparation conditions and of the atomic ratios between the metals on the structure and on the properties of the catalysts were studied. © 2003 Society of Chemical Industry [source] Ag-rich Tetrahedrite in the El Zancudo Deposit, Colombia: Occurrence, Chemical Compositions and Genetic TemperaturesRESOURCE GEOLOGY, Issue 3 2010Alba Nury Gallego Hernández Abstract Chemical compositions of tetrahedrite,Ag-rich tetrahedrite,freibergite solid solutions (Ag-rich tetrahedritess) and homogenization temperatures of fluid inclusions in quartz and carbonates of seventeen samples from nine veins in the El Zancudo deposit, Antioquia, Colombia, were investigated to reveal the origin of silver in Ag-rich tetrahedritess, to derive their crystallization temperatures and to examine the relationship between chemical compositions of Ag-rich tetrahedritess and their crystallization temperatures. The ores consist of arsenopyrite, pyrite, sphalerite, Ag-rich tetrahedritess, galena, boulangerite, andorite, owyheeite, diaphorite, jamesonite, miargyrite, bournonite, chalcopyrite, and electrum. Ag-rich tetrahedritess forms about 10 volume % of the total ores and is one of the most common and widely distributed sulfosalts in this deposit. Ag-rich tetrahedritess is rich in Ag (1.13 to 31.02 wt%) and Sb (22.93 to 29.82 wt%), and poor in As (0.06 to 2.43 wt%), consistent with the reported incompatibilities of Ag and As in Ag-rich tetrahedritess. The Zn/(Zn + Fe)-, Ag/(Ag + Cu)- and Sb/(Sb + As + Bi)-atomic ratios exhibit some variations among the veins. Ag-rich tetrahedritess with higher Ag/(Ag + Cu) ratios coexist with diaphorite, whereas those with lower ratios are not associated with this sulfosalt. Ag-rich tetrahedritess in the assemblages of Ag-rich tetrahedritess+ sphalerite and of Ag-rich tetrahedritess+ bournonite + galena shows no Zn , Fe and Cu , Ag variations between core and rim, respectively, negating the possibility of solid state reaction during cooling. Ag-rich tetrahedritess is thus regarded as primary phase. Homogenization temperatures of primary fluid inclusions in quartz and carbonates co-existing with Ag-rich tetrahedritess define the mineralization temperatures of 134 to 263°C. Independent crystallization temperatures of Ag-rich tetrahedrite estimated based on Zn/(Zn + Fe) and Ag/(Ag + Cu) ratios of the Ag-rich tetrahedritess associated with silver minerals such as miargyrite, andorite and diaphorite using Sack's thermochemical database lie in a range between 170 and ,250°C. Both results are thus in good agreement. [source] Hydrogenation of naphthalene on nickel phosphide supported on silicaASIA-PACIFIC JOURNAL OF CHEMICAL ENGINEERING, Issue 5 2009Xiaofei Zhang Abstract Two series of silica supported nickel phosphide catalysts with different Ni/P atomic ratios of the precursors and loadings had been prepared by a temperature-programmed reduction of nickel phosphate. The resulting samples were characterized by means of N2 physorption and X-ray diffraction (XRD). The activities of the catalysts were measured for naphthalene hydrogenation (HYD) at 340 °C and 4 MPa. The operating conditions of naphthalene HYD such as temperature, pressure and H2/liquor ratio were tested in detail. It is found that all the samples were active in this reaction and the sample which precursor with Ni/P = 1.25 and loading with 30 wt% displayed the highest catalytic activity and decalin selectivity. Naphthalene conversion and selectivity to decalin went through a maximum (100% and 83% at 340 °C) with the increasing reaction temperature. Copyright © 2009 Curtin University of Technology and John Wiley & Sons, Ltd. [source] | |||||||||||||