Home About us Contact
|
Home About us Contact | ||
|
|
||
Trivalent Cations (trivalent + cation)
Selected AbstractsThe Effect of Trivalent Cations on the Performance of Mg-M-CO3 Layered Double Hydroxides for High-Temperature CO2 CaptureCHEMSUSCHEM CHEMISTRY AND SUSTAINABILITY, ENERGY & MATERIALS, Issue 8 2010Qiang Wang Dr. Abstract The effect of trivalent cations on the performance of Mg-M-CO3 (M=Al, Fe, Ga, Mn) layered double hydroxides (LDHs) for high-temperature CO2 capture is systematically investigated for the first time. We demonstrate that the M3+ determines the structure evolution of LDH derivatives under thermal treatment, and finally influences the CO2 capture capacity. Very different calcination temperatures are required for the different LDHs to obtain their maximum CO2 capture capacities. To have a clear understanding of the reason behind these big differences the physicochemical properties, thermal stability, and memory effect of the LDHs were investigated. Both the thermal stability and the memory effect of LDHs are greatly influenced by the type of trivalent cation. The CO2 capture capacities were also evaluated under various conditions. Another important finding of this work is that the quasi-amorphous phase obtained by thermal treatment at the lowest possible temperature gives the highest CO2 capture capacity. [source] Citrate exudation from white lupin induced by phosphorus deficiency differs from that induced by aluminumNEW PHYTOLOGIST, Issue 3 2007B. L. Wang Summary ,,Both phosphorus (P) deficiency and aluminum (Al) toxicity induce root exudation of carboxylates, but the relationship between these two effects is not fully understood. Here, carboxylate exudation induced by Al in Lupinus albus (white lupin) was characterized and compared with that induced by P deficiency. ,,Aluminum treatments were applied to whole root systems or selected root zones of plants with limited (1 µm) or sufficient (50 µm) P supply. ,,Aluminum stimulated citrate efflux after 1,2 h; this response was not mimicked by a similar trivalent cation, La3+. P deficiency triggered citrate release from mature cluster roots, whereas Al stimulated citrate exudation from the 5- to 10-mm subapical root zones of lateral roots and from mature and senescent cluster roots. Al-induced citrate exudation was inhibited by P limitation at the seedling stage, but was stimulated at later growth stages. Citrate exudation was sensitive to anion-channel blockers. Al treatments did not affect primary root elongation, but inhibited the elongation of lateral roots. ,,The data demonstrate differential patterns of citrate exudation in L. albus, depending on root zone, developmental stage, P nutritional status and Al stress. These findings are discussed in terms of possible functions and underlying mechanisms. [source] New vanadium(IV) and titanium(IV) oxyfluorotellurates(IV): V2Te2O7F2 and TiTeO3F2ACTA CRYSTALLOGRAPHICA SECTION C, Issue 1 2009Jean Paul Laval As part of a continuing study of oxyfluorotellurates(IV), materials likely to present interesting nonlinear optical properties, two new phases, titanium(IV) tellurium(IV) trioxide difluoride, TiTeO3F2, and divanadium(IV) ditellurium(IV) heptaoxide difluoride, V2Te2O7F2, have been characterized and present, respectively, titanium and vanadium in the tetravalent state. The TiTeO3F2 structure is based on linear double rows of TiO3F3 polyhedra sharing vertices. These rows are connected to adjacent rows via two vertices of Te2O5 bipolyhedra. The Te, Ti, one F and two O atoms are on general positions, with one O and F statistically occupying the same site with half-occupancy for each anion. One O and one F occupy sites with .m. symmetry. The V2Te2O7F2 structure consists of zigzag chains of VO4F2 octahedra alternately sharing O,O and F,F edges. These chains are connected via Te2O5 bipolyhedra, forming independent mixed layers. The Te, V, one F and three O atoms are on general positions while one O atom occupies a site of symmetry. In both phases, the electronic lone pair E of the TeIV atom is stereochemically active. A full O/F anionic ordering is observed in V2Te2O7F2, but in TiTeO3F2 one of the six anionic sites is occupied by half oxygen and half fluorine, all the others being strictly ordered. These compounds represent new members of a growing family of oxyfluorotellurates(IV), including the recently characterized members of formula MTeO3F, M being a trivalent cation. As was true for the previous members, they are characterized by an unusually high thermal and chemical stability in relation to the absence of direct Te,F bonds. [source] The Effect of Trivalent Cations on the Performance of Mg-M-CO3 Layered Double Hydroxides for High-Temperature CO2 CaptureCHEMSUSCHEM CHEMISTRY AND SUSTAINABILITY, ENERGY & MATERIALS, Issue 8 2010Qiang Wang Dr. Abstract The effect of trivalent cations on the performance of Mg-M-CO3 (M=Al, Fe, Ga, Mn) layered double hydroxides (LDHs) for high-temperature CO2 capture is systematically investigated for the first time. We demonstrate that the M3+ determines the structure evolution of LDH derivatives under thermal treatment, and finally influences the CO2 capture capacity. Very different calcination temperatures are required for the different LDHs to obtain their maximum CO2 capture capacities. To have a clear understanding of the reason behind these big differences the physicochemical properties, thermal stability, and memory effect of the LDHs were investigated. Both the thermal stability and the memory effect of LDHs are greatly influenced by the type of trivalent cation. The CO2 capture capacities were also evaluated under various conditions. Another important finding of this work is that the quasi-amorphous phase obtained by thermal treatment at the lowest possible temperature gives the highest CO2 capture capacity. [source] In situ study of growth and dissolution kinetics of ammonium oxalate monohydrate single crystals from aqueous solutions containing cationic impuritiesCRYSTAL RESEARCH AND TECHNOLOGY, Issue 12 2007K. Sangwal Abstract The results of an in situ investigation of the effect of four different bi- and trivalent cations (Fe(III), Cu(II), Mn(II) and Cr(III)) on the displacement velocity of individual growth steps on the (110) face of ammonium oxalate monohydrate crystals as a function of supersaturation are described and discussed. It was observed that: (1) at a particular temperature of pure solutions and solutions containing impurities, the velocity v of movement of the [110] growth steps is always greater than that of the [111] steps, (2) fluctuations in the velocity of individual growth steps occur in all solutions containing similar concentrations of different impurities, (3) the value of kinetic coefficient , for growth steps decreases with an increase in the concentration ci of Cu(II) impurity, but that for dissolution steps does not depend on ci; moreover, the value of kinetic coefficient , for growth steps is higher than that of dissolution steps, and (4) in the presence of Mn(II) and Cr(III) impurities, the kinetic coefficient , for dissolution steps is several times greater than that for growth steps. The results are explained from the standpoint of Kubota-Mullin model of adsorption of impurities at kinks in the steps and the stability of dominating complexes present in solutions. Analysis of the results revealed that: (1) the effectiveness of different impurities in inhibiting growth increases in the order: Fe(III), Cu(II), Mn(II), and Cr(III), and this behavior is directly connected with the stability and chemical constitution of dominating complexes in saturated solutions, (2) fluctuations in the velocity of growth steps is associated with the effectiveness of an impurity for adsorption; the stronger the adsorption of an impurity, the higher is the fluctuation in step velocity v, and (3) depending on the nature of the impurity, the kinetic coefficient for the dissolution steps can remain unchanged or can be higher than that of the growth steps. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Understanding the binding properties of an unusual metal-binding protein , a study of bacterial frataxinFEBS JOURNAL, Issue 16 2007Chiara Pastore Deficiency of the small mitochondrial protein frataxin causes Friedreich's ataxia, a severe neurodegenerative pathology. Frataxin, which has been highly conserved throughout evolution, is thought to be involved in, among other processes, Fe,S cluster formation. Independent evidence shows that it binds iron directly, although with very distinct features and low affinity. Here, we have carried out an extensive study of the binding properties of CyaY, the bacterial ortholog of frataxin, to different divalent and trivalent cations, using NMR and X-ray crystallography. We demonstrate that the protein has low cation specificity and contains multiple binding sites able to chelate divalent and trivalent metals with low affinity. Binding does not involve cavities or pockets, but exposed glutamates and aspartates, which are residues that are unusual for iron chelation when not assisted by histidines and/or cysteines. We have related how such an ability to bind cations on a relatively large area through an electrostatic mechanism could be a valuable asset for protein function. [source] Plasma phospholipids implicated in the matrix effect observed in liquid chromatography/tandem mass spectrometry bioanalysis: evaluation of the use of colloidal silica in combination with divalent or trivalent cations for the selective removal of phospholipids from plasmaRAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 18 2008Steven T. Wu The feasibility of the use of colloidal silica in combination with a number of divalent or trivalent cations for the removal of plasma phospholipids was evaluated by sequentially adding the two reagents (i.e., colloidal silica and a cation) directly to blank plasma samples or plasma samples spiked with analytes. Three representative plasma phospholipids were monitored to determine the efficiency of the phospholipids removal under different reagent combinations. The recovery of each spiked analyte was also monitored under each condition in order to determine if any of the analyte was removed along with the phospholipids. By optimizing the amounts of the reagents used and the sequence of the addition of the reagents, quantitative and reproducible removal of the phospholipids was achieved. Using the finally selected lanthanum cation, the removal of phospholipids was achieved with minimal concomitant loss of the ten investigated analytes which were carefully selected to incorporate functional groups that could potentially interact with the added reagents and hence could be removed along with the phospholipids. Copyright © 2008 John Wiley & Sons, Ltd. [source] The Effect of Trivalent Cations on the Performance of Mg-M-CO3 Layered Double Hydroxides for High-Temperature CO2 CaptureCHEMSUSCHEM CHEMISTRY AND SUSTAINABILITY, ENERGY & MATERIALS, Issue 8 2010Qiang Wang Dr. Abstract The effect of trivalent cations on the performance of Mg-M-CO3 (M=Al, Fe, Ga, Mn) layered double hydroxides (LDHs) for high-temperature CO2 capture is systematically investigated for the first time. We demonstrate that the M3+ determines the structure evolution of LDH derivatives under thermal treatment, and finally influences the CO2 capture capacity. Very different calcination temperatures are required for the different LDHs to obtain their maximum CO2 capture capacities. To have a clear understanding of the reason behind these big differences the physicochemical properties, thermal stability, and memory effect of the LDHs were investigated. Both the thermal stability and the memory effect of LDHs are greatly influenced by the type of trivalent cation. The CO2 capture capacities were also evaluated under various conditions. Another important finding of this work is that the quasi-amorphous phase obtained by thermal treatment at the lowest possible temperature gives the highest CO2 capture capacity. [source] | ||||||||||