Gas–Solid Exchange Reaction: Zinc Vapor and Polycrystalline Zinc Orthosilicate

1974 ◽  
Vol 52 (23) ◽  
pp. 3932-3935 ◽  
Author(s):  
Etalo A. Secco ◽  
Hari Pada Dhar ◽  
Chien-Huo Su
Keyword(s):  
Initial Rate ◽  
Particle Growth ◽  
Static System ◽  
Zinc Vapor ◽  
Rate Laws ◽  
Zinc Orthosilicate ◽  
Polycrystalline Zinc ◽  
High Annealing ◽  
Exchange Kinetics ◽  
Kinetics Of

The exchange kinetics of zinc vapor with polycrystalline zinc orthosilicate have been studied in a static system in the temperature range 760–1000 °C.The kinetic data reveal two rate laws. The initial rate is assigned to a transport step, i.e. mobility of zinc with D = 10−8 exp (−34 ± 5 kcal/RT ) cm2 s−1. The rate at high annealing times is a composite of the initial rate and a particle growth process, e.g. sintering.

GAS–SOLID EXCHANGE REACTIONS: ZINC VAPOR AND POLYCRYSTALLINE ZINC SULPHIDE

1964 ◽  
Vol 42 (6) ◽  
pp. 1396-1400 ◽  
Author(s):  
E. A. Secco
Keyword(s):  
Zinc Sulphide ◽  
Static System ◽  
Zinc Vapor ◽  
Exchange Reactions ◽  
Polycrystalline Zinc ◽  
Diffusion Controlled ◽  
Fraction Versus ◽  
Exchange Kinetics ◽  
Kinetics Of ◽  
Initial Process

The exchange kinetics of zinc vapor with polycrystalline zinc sulphide, wurtzite structure, have been studied in a static system in the temperature range 720–960 °C.Plots of log10(1−α*), i.e. exchange fraction, versus time reveal two processes. The initial process is a rapid simple exchange, for which the data fit a first-order rate law and which persists to a depth of 15–18 molecular thicknesses. At this depth the second, slower process, which appears to be diffusion-controlled, sets in. Kinetic and structural interpretations of these results along with the existing data on Zn–ZnO exchange are discussed.

Gas–solid exchange reactions: Zinc vapor and polycrystalline zinc selenide

1968 ◽  
Vol 46 (10) ◽  
pp. 1621-1624 ◽  
Author(s):  
E. A. Secco ◽  
Chien-Huo Su
Keyword(s):  
Zinc Selenide ◽  
Static System ◽  
Zinc Vapor ◽  
Exchange Reactions ◽  
Polycrystalline Zinc ◽  
Diffusion Controlled ◽  
Initial Stage ◽  
Exchange Kinetics ◽  
Kinetics Of ◽  
Exchange Data

The exchange kinetics of zinc vapor with polycrystalline zinc selenide have been studied in a static system in the temperature range 720–800 °C.The kinetic data are consistent with a diffusion-controlled process from the initial stage, in contrast with existing exchange data on ZnO and ZnS powders. The diffusion equation is given as:[Formula: see text]

scholarly journals Thermodynamic and detailed kinetic study of the formation of orthophthalaldehyde-agmatine complex by fluorescence intensities

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Khémesse Kital ◽  
Moumouny Traoré ◽  
Diégane Sarr ◽  
Moussa Mbaye ◽  
Mame Diabou Gaye Seye ◽  
...  
Keyword(s):  
Complex Formation ◽  
Thermodynamic Parameters ◽  
Initial Rate ◽  
Reaction Medium ◽  
Standard Entropy ◽  
Step Size ◽  
Formation Reaction ◽  
Different Temperatures ◽  
Kinetics Of ◽  
Complex Formation Process

Abstract The aim of this work is to determine the thermodynamic parameters and the kinetics of complex formation between orthophthalaldehyde (OPA) and agmatine (AGM) in an alkaline medium (pH 13). Firstly, the association constant (Ka) between orthophthalaldehyde and agmatine was determined at different temperatures (between 298 K and 338 K) with a step size of 10 K. Secondly, the thermodynamic parameters such as standard enthalpy (ΔH°), standard entropy (ΔS°),and Gibbs energy (∆G) were calculated, where a positive value of ΔH° (+45.50 kJ/mol) was found, which shows that the reaction is endothermic. In addition, the low value of ΔS°(+0.24 kJ/mol) indicates a slight increase in the disorder in the reaction medium. Furthermore, the negative values of ΔG between −35.62 kJ/mol and −26.02 kJ/mol show that the complex formation process is spontaneous. Finally, the parameters of the kinetics of the reaction between OPA and AGM were determined as follows: when the initial concentration of AGM (5 × 10−6 M) is equal to that of the OPA, the results show that the reaction follows an overall 1.5 order kinetics with an initial rate of 5.1 × 10−7Mmin−1 and a half-life of 8.12 min. The partial order found in relation to the AGM is 0.8. This work shows that the excess of OPA accelerates the formation reaction of the complex.

Fast oxygen exchange kinetics of pore-free Bi1−xSrxFeO3−δ thin films

2011 ◽  
Vol 13 (37) ◽  
pp. 16530 ◽  
Author(s):  
Anja Wedig ◽  
Rotraut Merkle ◽  
Benjamin Stuhlhofer ◽  
Hanns-Ulrich Habermeier ◽  
Joachim Maier ◽  
...  
Keyword(s):  
Thin Films ◽  
Oxygen Exchange ◽  
Exchange Kinetics ◽  
Kinetics Of

scholarly journals Hydrogen exchange kinetics of human hemoglobins. The pH dependence of solvent accessibility in cyanomet-, oxy-, and deoxyhemoglobin.

1978 ◽  
Vol 253 (10) ◽  
pp. 3702-3707
Author(s):  
B.E. Hedlund ◽  
P.E. Hallaway ◽  
B.E. Hallaway ◽  
E.S. Benson ◽  
A. Rosenberg
Keyword(s):  
Hydrogen Exchange ◽  
Solvent Accessibility ◽  
Ph Dependence ◽  
Exchange Kinetics ◽  
Kinetics Of

Chain Exchange Kinetics of Bottlebrush Block Copolymer Micelles

2021 ◽  
Author(s):  
Seyoung Kim ◽  
Sangho Lee ◽  
Soo-Hyung Choi ◽  
Kookheon Char
Keyword(s):  
Block Copolymer ◽  
Block Copolymer Micelles ◽  
Exchange Kinetics ◽  
Copolymer Micelles ◽  
Kinetics Of

scholarly journals Influence of Heterointerfaces on the Kinetics of Oxygen Surface Exchange on Epitaxial La1.85Sr0.15CuO4 Thin Films

2021 ◽  
Vol 11 (9) ◽  
pp. 3778
Author(s):  
Gene Yang ◽  
So-Yeun Kim ◽  
Changhee Sohn ◽  
Jong K. Keum ◽  
Dongkyu Lee
Keyword(s):  
Thin Films ◽  
Oxygen Vacancies ◽  
Elevated Temperatures ◽  
Surface Exchange ◽  
Electrical Conductivity Relaxation ◽  
Exchange Kinetics ◽  
Relaxation Curves ◽  
Kinetics Of ◽  
Oxygen Surface Exchange ◽  
Oxygen Surface

Considerable attention has been directed to understanding the influence of heterointerfaces between Ruddlesden–Popper (RP) phases and ABO3 perovskites on the kinetics of oxygen electrocatalysis at elevated temperatures. Here, we report the effect of heterointerfaces on the oxygen surface exchange kinetics by employing heteroepitaxial oxide thin films formed by decorating LaNiO3 (LNO) on La1.85Sr0.15CuO4 (LSCO) thin films. Regardless of LNO decoration, tensile in-plane strain on LSCO films does not change. The oxygen surface exchange coefficients (kchem) of LSCO films extracted from electrical conductivity relaxation curves significantly increase with partial decorations of LNO, whereas full LNO coverage leads to the reduction in the kchem of LSCO films. The activation energy for oxygen exchange in LSCO films significantly decreases with partial LNO decorations in contrast with the full coverage of LNO. Optical spectroscopy reveals the increased oxygen vacancies in the partially covered LSCO films relative to the undecorated LSCO film. We attribute the enhanced oxygen surface exchange kinetics of LSCO to the increased oxygen vacancies by creating the heterointerface between LSCO and LNO.

Hydrogen exchange kinetics of core peptide protons in Streptomyces subtilisin inhibitor

Biochemistry ◽  
1985 ◽  
Vol 24 (12) ◽  
pp. 2973-2979 ◽  
Author(s):  
Kazuyuki Akasaka ◽  
Tomoko Inoue ◽  
Hiroyuki Hatano ◽  
Clare K. Woodward
Keyword(s):  
Hydrogen Exchange ◽  
Core Peptide ◽  
Exchange Kinetics ◽  
Subtilisin Inhibitor ◽  
Kinetics Of
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