Home About us Contact
|
Home About us Contact | ||
|
|
||
Formation Kinetics (formation + kinetics)
Selected AbstractsFormation Kinetics of a Bi3Nb1,xTaxO7 Fluorite-Type Solid Solution and Thermodynamic Stability of the Bi3TaO7 End MemberJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 9 2010Ursa Pirnat Analysis of kinetic characteristics of the incommensurate,commensurate transformation in the Bi3Nb1,xTaxO7 system with a fluorite-like crystal structure enabled us to define the compositional and thermal stability ranges of the commensurate tetragonal polymorph. We showed that the tetragonal polymorph across the entire homogeneity range is isostructural to the Bi3NbO7 end member. The kinetics of the transformation from the cubic incommensurate to the tetragonal commensurate phase decreases with an increase in Ta concentration within the Bi3Nb1,xTaxO7 system. The formation studies indicate that the tetragonal Bi3TaO7 is thermodynamically stable; however, its formation via the metastable incommensurate-cubic phase is suppressed. [source] Extracellular phosphatase activity of natural plankton studied with ELF97 phosphate: fluorescence quantification and labelling kineticsENVIRONMENTAL MICROBIOLOGY, Issue 6 2003í Nedoma Summary ELF®97 phosphate (ELFP) is a phosphatase substrate which produces ELF®97 alcohol (ELFA), a fluorescent water-insoluble product, upon hydrolysis. We studied the kinetics of ELFA precipitation in freshwater samples at levels of total plankton and single phytoplankton cells, and tested the suitability of ELFP for measurement of surface-bound algal extracellular phosphatases. Samples from acidic Ple,né Lake (pH , 5; high phosphatase activity) and eutrophic ,ímov reservoir (pH ,7,10; moderate phosphatase activity) were incubated with ELFP for 5,300 min, fixed with HgCl2 and filtered through polycarbonate filters. Relative fluorescence of filter-retained ELFA precipitates was quantified with image analysis. Time-courses of ELFA formation exhibited lag periods followed by finite periods of linear increase. In Ple,né Lake, lag-times were shorter (1,18 min) and rates of increase in ELFA fluorescence higher (by ,2 orders of magnitude) than in ,ímov reservoir (lag-times 30,200 min). Similar patterns of ELFA formation kinetics were also observed in Ple,né Lake samples in cuvette spectrofluorometer measurements (which failed in ,ímov reservoir). Linear regression of seasonal data on rates of increase in ELFA fluorescence from image cytometry and spectrofluorometry (r2 = 0.65, n = 10) allowed for calibration of image cytometry in terms of amount of cell-associated ELFA. Preliminary measurements of extracellular phosphatase activities of several algae resulted in rates (10,2260 fmol cell,1 h,1) which are comparable to data reported in the literature for algal cultures. [source] Kinetics and Mechanism of Formation of Barium Zirconate from Barium Carbonate and Zirconia PowdersJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2003Alberto Ubaldini The formation of BaZrO3 from very fine (70,90 nm) ZrO2 powders and coarser (,1 ,m) BaCO3 powders has been studied in dry and humid air up to 1300°C using TGA/DTA, XRD, SEM, TEM, and EDS microanalysis. In the temperature range 900°,1100°C, barium is rapidly transported at the surface of the ZrO2 particles and reacts, forming BaZrO3. The compound grows as a concentric layer with gradual consumption of the central ZrO2 particle. The overall formation kinetics of BaZrO3 is well described by a diminishing core model, and the most likely rate-determining step is a phase-boundary process at the ZrO2,BaZrO3 moving interface. The size and shape of the final particles is generally determined by the morphology of the starting ZrO2 particles and not by that of the BaCO3. The reaction is faster in humid air than in dry air, and the activation energy decreases from 294 kJ·mol,1 (dry air) to 220 kJ·mol,1 (humid air). When the fraction reacted is >80,90 mol%, the reaction rate rapidly decreases. [source] A universal alternating immersion simulator for accelerated cyclic corrosion tests,MATERIALS AND CORROSION/WERKSTOFFE UND KORROSION, Issue 2 2008A. W. Hassel A new device for performing accelerated cyclic immersion tests is described. The main achievement is to realise a high cycling rate without a proportional increase in the test duration. The device is also capable of performing tests according to EU ISO 11130 specification. A minimal invasive drying system is used that neither heats air nor sample and the flow rate is still low as to prevent a mechanical delamination of paints or loose corrosion products. A multiple sample set-up is realised that provides individual reference electrodes. The random access through a multiplexer allows individual investigation of the samples even by electrochemical impedance spectroscopy under immersion conditions. The device and its test principle are applicable in both industrial and laboratorial scale applications. Two application examples are given to demonstrate the versatility of the alternating immersion tester. One addresses the corrosion protection performance of different zinc-coated steel sheets; the other quantifies the patina formation kinetics of low-alloyed steels with weathering properties. [source] Composition and formation mechanism of zirconium oxynitride films produced by reactive direct current magnetron sputteringPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 5 2004J. M. Ngaruiya Abstract Direct current magnetron sputtered zirconium oxynitride films show an improvement in both deposition rate and physical properties compared to zirconium oxide. Here we seek to understand these beneficial effects and report on the film composition and crystallographic structure. Based on a thermochemical description together with a modeling of formation kinetics we propose a film formation mechanism, which explains many of the observations. Rutherford backscattering spectroscopy (RBS) shows early nitrogen incorporation at 64% N2 flow in disagreement with the predictions of thermochemistry. The stoichiometry is only successfully simulated with the use of an expanded Berg,Larsson model with a low replacement coefficient of about 0.1 of nitrogen by oxygen after metal-nitrogen bond formation. The deviation from complete replacement as predicted by thermodynamics illustrates the importance of kinetics in film formation. The model further successfully predicts the variation of the mass deposition rate. The X-ray diffraction analyses suggest that, within the crystalline phase, nitrogen atoms occupy oxygen sites, resulting in an unchanged zirconium oxide structure. (© 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] In situ ellipsometric studies of formation kinetics of rare earth metal conversion coatings on magnesium alloyPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 5 2008Lingjie Li Abstract In situ spectroscopic ellipsometry was employed to investigate the initial regime of rare earth metal (REM) conversion coatings formation on AZ31 magnesium alloy. Three REM salts solutions, 0.05 mol·dm -3 Ce(NO3)3, La(NO)3 and Sm(NO)3 solutions, were used for REM conversion coatings preparation. By deconvoluting the ellipsometric data, the surface of the fresh well-polished AZ31 magnesium alloy was found to be covered with 15.80 nm thick native (hydr)oxide film; the refractive indices and the thickness of Ce, La and Sm conversion coatings were obtained. The formation kinetics of three REM coatings follows different exponential functions and the coatings exhibit different optical properties. La conversion coating has the largest n values and the lowest k values while Sm conversion coating is just opposite. Moreover, the pH variation of the bulk conversion solutions upon the coatings formation was recorded. It is confirmed that the reduction of protons leads to the interfacial pH increasing and further results in the precipitation of REM hydroxide gel, which is critical for the REM conversion coatings formation. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Synthesis and characterization of polyurethane/polybenzoxazine-based interpenetrating polymer networks (IPNs)POLYMER INTERNATIONAL, Issue 8 2003Yanjun Cui Abstract Sequential interpenetrating polymer networks (IPNs), based on polyurethane and polybenzoxazine, were synthesized. Fourier Transform infrared spectrometry was employed to monitor the formation kinetics, which indicated that only physical bonding existed in the resulting IPNs. Morphological investigations revealed a lightly phase separation behaviour in all of the IPNs studied. © 2003 Society of Chemical Industry [source] Effects of surfactant and molecular weight of polyol on grating formation and switching of holographic PDLCPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 11 2008S. S. Shim Abstract The interposition of surfactants between polymer and liquid crystal (LC) droplets was theoretically predicted by the positive spreading coefficient (0,<,,31) and utilized to interpret the morphology, grating formation kinetics, diffraction efficiency, and switching of the holographic polymer dispersed liquid crystal (HPDLC), prepared from various types (octanoic acid, poly oxyethylene octyl phenyl ether, and perfluoro-1-butanesulfonyl fluoride) and amounts (0,9 wt%) of surfactant and molecular weights of polyol (PPG). Regardless of the surfactant type, diffraction efficiency increased with the addition and increasing amount of surfactant, a tendency consistent with increasing value of spreading coefficient, which is determined by the formulations of grating formation. In contrast, diffraction efficiency showed a maximum with the polypropylene glycol (PPG) molecular weight. Surfactant effectively reduced the anchoring energy and electrically drove the film which otherwise was not driven. Overall, surfactant with greater ,31 gave smaller droplet, greater diffraction efficiency, driving voltage, contrast ratio, and smaller response time. Copyright © 2008 John Wiley & Sons, Ltd. [source] Study of the Kinetics and Morphology of Gas Hydrate FormationCHEMICAL ENGINEERING & TECHNOLOGY (CET), Issue 8 2006Abstract The kinetics and morphology of ethane hydrate formation were studied in a batch type reactor at a temperature of ca. 270,280,K, over a pressure range of 8.83,16.67,bar. The results of the experiments revealed that the formation kinetics were dependant on pressure, temperature, degree of supercooling, and stirring rate. Regardless of the saturation state, the primary nucleation always took place in the bulk of the water and the phase transition was always initiated at the surface of the vortex (gas-water interface). The rate of hydrate formation was observed to increase with an increase in pressure. The effect of stirring rate on nucleation and growth was emphasized in great detail. The experiments were performed at various stirring rates of 110,190,rpm. Higher rates of formation of gas hydrate were recorded at faster stirring rates. The appearance of nuclei and their subsequent growth at the interface, for different stirring rates, was explained by the proposed conceptual model of mass transfer resistances. The patterns of gas consumption rates, with changing rpm, have been visualized as due to a critical level of gas molecules in the immediate vicinity of the growing hydrate particle. Nucleation and decomposition gave a cyclic hysteresis-like phenomena. It was also observed that a change in pressure had a much greater effect on the rate of decomposition than it did on the formation rate. Morphological studies revealed that the ethane hydrate resembles thread or is cotton-like in appearance. The rate of gas consumption during nucleation, with different rpm and pressures, and the percentage decomposition at different pressures, were explained precisely for ethane hydrate. [source] | |||||||||||||