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161.
T. Vlase Gabriela Vlase A. Chiriac N. Doca 《Journal of Thermal Analysis and Calorimetry》2005,80(1):87-90
Summary In order to obtain catalysts, the thermal decomposition of the precursors is a compulsory step. However, kinetic analysis of the decomposition data obtained under non-isothermal conditions lead very seldom to the intimate reaction mechanism. There is also a lack of information because in non-isothermal kinetics, the compensation effect, is rather a rule and unfortunately a source of debate. In order to discriminate between these processes, and the influence of conversion, respectively temperature on the reaction rate, the NPK (non-parametric kinetic - Sempere and Nomen) method was used. This method is based on the singular value decomposition algorithm (SVD) applied on the matrix of reaction rate at corresponding conversion and temperature. This method allows a less speculative determination of the conversion functions and of the kinetic parameters. 相似文献
162.
This work describes a structure and kinetic stability study of some complexes with the general formula MN, where M are the alkaline earth metal atoms, Be, Mg, Ca, Sr, and Ba. A complex (A) with two points of attachment to the N5 ring is the most energetically favored for all metals considered here. Except for Be, structure (B) containing a mono‐coordinated metal atom is a transition state corresponding to the metal atom transfer around the N5 ring. Pyramidal structure (C) is kinetically unstable with the low isomerization barrier height, ranging from 0.9 to 6.7 kcal/mol. The dissociation barrier heights for the lowest energy isomers (A) are predicted to be 1.2–18.7 kcal/mol (Be to Ba), indicating that kinetic stability increases from lighter to heavier metal atoms. © 2004 Wiley Periodicals, Inc. Int J Quantum Chem, 2004 相似文献
163.
Analyte transfer from the matrix in a thin layer distillation (TLD) cell and its subsequent measurement were investigated in a flow injection configuration. We designed the cell such that the donor and acceptor streams flowed in parallel channels separated by a thin dividing wall. The matrix transfer process involved room-temperature distillation of the analyte into the headspace of the TLD cell and its subsequent condensation/uptake by a concurrently flowing acceptor stream. There are no membranes; hence there are no membrane-related problems. The TLD system design was optimized with respect to its dimensions and operational parameters. Throughput and sensitivity were compared with a conventional pervaporation flow injection (PFI) system for ammonia and five different amines. For the higher molecular mass amines, the TLD approach provided comparable or superior performance. The TLD technique should be an attractive approach for online analysis of volatile chemical species in ‘dirty’ samples, especially for volatile analytes of higher molecular mass. 相似文献
164.
Kzysztof Schmidt-Szałowski Anna Borucka Sławomir Jodzis 《Plasma Chemistry and Plasma Processing》1990,10(3):443-450
The catalytic action of granular silica packing on ozone formation has been observed under discharge conditions. Using a glass ozonizer with a metal high-voltage electrode, at a frequency of 400 Hz it was possible to obtain much higher ozone concentrations in the presence q( silica than without packing, with the same total energy consumption. The dependence between ozone production and energy efficiency is considered, and conditions of the optimum ozonizer run are discussed. It is shown that in the all-glass ozonizer with a narrow discharge gap, the ozone concentration may be as high as 6.5% (ca. 130g O3/m3) when silica packing is applied. 相似文献
165.
A spectrophotometric method has been developed for the simultaneous determination ofo-cresol andm-cresol in water by reaction withp-aminophenol (PAP). Three different methodologies have been assayed; (i) batch analysis, after reaction in an alkaline medium in the presence of dissolved molecular oxygen as oxidizing agent, (ii) a stopped-flow procedure, carried out in the presence of KIO4 and (iii) a flow injection method based on the same approach. The batch procedure requires 22 min for the full development of colour witho-cresol and 12 min form-cresol. In the stopped-flow mode, using KIO4 and a reaction time of 12 min, better sensitivity can be obtained for both compounds and limits of detection of 10 g 1–1 foro-cresol and 30 g 1–1 form-cresol were found. The flow injection method has a lower sensitivity but permits more than 80 injections per hour. Based on the different maximum absorbance wavelengths obtained for the reaction products of PAP witho-cresol (614 nm) andm-cresol (632 nm), both compounds can be simultaneously determined in water samples and recoveries of 90 to 115% were found in spiked water samples of different types. 相似文献
166.
A new catalytic kinetic spectrophotometric method has been developed for the determination of trace amount of manganese (II) in nonionic microemulsion medium. The method is based on the catalytic effect of manganese (II) on the oxidation of dahlia violet by potassium periodate with nitrilotriacetic acid as an activitor in the presence of nonionic microemulsion. Under the optimum conditions, the calibration graph is linear in the range of 0.0004-0.0056 μg ml−1 of manganese (II) at 580 nm. The detection limit achieved is 3.75×10−5 μg ml−1. Manganese (II) in foodstuff samples was determined with satisfactory results. 相似文献
167.
A mathematical model of amperometric biosensors has been developed. The model is based on non-stationary diffusion equations containing a non-linear term related to Michaelis–Menten kinetic of the enzymatic reaction. Using digital simulation, the influence of the substrate concentration as well as maximal enzymatic rate on the biosensor response was investigated. The digital simulation was carried out using the finite difference technique. The model describes the biosensor action in batch and flow injection regimes. 相似文献
168.
Krasnov V. P. Levit G. L. Korolyova M. A. Bukrina I. M. Sadretdinova L. Sh. Andreeva I. N. Charushin V. N. Chupakhin O. N. 《Russian Chemical Bulletin》2004,53(6):1253-1256
The influence of the reaction conditions (solvent, base) on the diastereoselectivity of acylation of (±)-3-methyl-2,3-dihydro-4H-1,4-benzoxazine with (S)-naproxen and N-tosyl-(S)-proline chlorides was studied. The highest diastereoselectivity was observed for the reaction carried out in benzene in the presence of aliphatic tertiary amines. 相似文献
169.
Ning Zhang Qing-Cheng Kong Zhen-Zhen Chen Ke-Hua Xu Bo Tang 《Mikrochimica acta》2007,158(1-2):165-171
A sensitive catalytic kinetic spectrofluorimetric approach for determining ng mL−1 levels of rhodium is presented, and the possible mechanism of the catalytic reaction was investigated. The determination
is based on the catalytic property of rhodium to enhance the reaction of o-vanillin salicylhydrazone (OVSH) with potassium
bromate in a water-ethanol medium at pH 4.80 and 45 °C. The presence of β-cyclodextrin (β-CD) obviously sensitized the assay
due to its high inclusion ability towards OVSH. Under optimized experimental conditions, fluorescence measurements of the
β-CD-rhodium-KBrO3-OVSH catalytic kinetic reaction system were carried out in its fluorescent band centered at λex = 333 nm and λem = 476 nm, respectively. The calibration graph was linear over the concentration range of 0.47–100 ng mL−1 with a detection limit of 0.14 ng mL−1. The effect of interferences was discussed, and the results show that the extraction method can be used to separate rhodium
from interference species such as iridium. The proposed method, applied to several synthetic mixtures containing rhodium mixed
with varying amounts of metal salts, produced satisfactory results. 相似文献
170.
Since hollow-fiber flow field-flow fractionation (HF FIFFF) utilizes a cylindrical channel made of a hollow-fiber membrane, which is inexpensive and simple in channel assembly and thus disposable, interests are increasing as a potential separation device in cells, proteins, and macromolecules. In this study, performance of HF FIFFF of proteins is described by examining the influence of flow rate conditions and length of fiber (polyacrylonitrile or PAN in this work) on sample recovery as well as experimental plate heights. The interfiber reproducibility in terms of separation time and recovery was also studied. Experiments showed that sample recovery was consistent regardless of the length of fiber when the effective field strength (equivalent to the mean flow velocity at the fiber wall) and the channel void time were adjusted to be equivalent for channels of various fiber lengths. This supported that the majority of sample loss in HF FIFFF separation of apoferritin and their aggregates may occur before the migration process. It is finally demonstrated that HF FIFFF can be applied for characterizing the reduction in Stokes' size of low density lipoproteins from blood plasma samples obtained from patients having coronary artery disease and from healthy donors. 相似文献