scholarly journals Origin of Pseudo Second Order Reaction in a-Si:H Growth

2017 ◽  
Vol 15 (0) ◽  
pp. 93-95 ◽  
Author(s):  
Yasutake Toyoshima
Keyword(s):  
Order Reaction ◽  
Second Order ◽  
Second Order Reaction ◽  
Pseudo Second Order

Stability of radical anions derived from substituted 5-nitrofurans investigated by ESR spectroscopy

1985 ◽  
Vol 50 (7) ◽  
pp. 1594-1601 ◽  
Author(s):  
Jiří Klíma ◽  
Larisa Baumane ◽  
Janis Stradinš ◽  
Jiří Volke ◽  
Romualds Gavars
Keyword(s):  
Radical Anion ◽  
High Stability ◽  
Esr Spectroscopy ◽  
Reaction Path ◽  
Order Reaction ◽  
Second Order ◽  
Radical Anions ◽  
Second Order Reaction ◽  
Unpaired Electron Density ◽  
The Stability

It has been found that the decay in dimethylformamide and dimethylformamide-water mixtures of radical anions in five of the investigated 5-nitrofurans is governed by a second-order reaction. Only the decay of the radical anion generated from 5-nitro-2-furfural III may be described by an equation including parallel first- and second-order reactions; this behaviour is evidently caused by the relatively high stability of the corresponding dianion, this being an intermediate in the reaction path. The presence of a larger conjugated system in the substituent in position 2 results in a decrease of the unpaired electron density in the nitro group and, consequently, an increase in the stability of the corresponding radical anions.

Kinetics of the reaction between hexamethylenediisocyanate and 1-pentanol

1983 ◽  
Vol 48 (11) ◽  
pp. 3279-3286
Author(s):  
Slavko Hudeček ◽  
Miloslav Bohdanecký ◽  
Ivana Hudečková ◽  
Pavel Špaček ◽  
Pavel Čefelín
Keyword(s):  
Liquid Chromatography ◽  
Rate Constants ◽  
Reversed Phase ◽  
Order Reaction ◽  
Second Order ◽  
Second Order Reaction ◽  
Reversed Phase Liquid Chromatography ◽  
Consecutive Reactions ◽  
Phase Liquid ◽  
Kinetics Of

The reaction between hexamethylenediisocyanate and 1-pentanol in toluene was studied by means of reversed-phase liquid chromatography. By employing this method, it was possible to determine all components of the reaction mixture including both products, i.e. N-(6-isocyanate hexyl)pentylcarbamate and N,N'-bis(pentyloxycarbonyl)hexamethylenediamine. Relations for the calculation of kinetic constants were derived assuming a competitive consecutive second-order reaction. It was demonstrated that the reaction involved in this case is indeed a second-order reaction, and the rate constants of the first and second consecutive reactions were determined.

Analytical resolution of a parallel second-order reaction mechanism

2003 ◽  
Vol 35 (6) ◽  
pp. 246-251
Author(s):  
A. E. Croce ◽  
L. V. Mogni ◽  
C. Vicente Irrazábal
Keyword(s):  
Reaction Mechanism ◽  
Order Reaction ◽  
Second Order ◽  
Second Order Reaction ◽  
Analytical Resolution

scholarly journals Ribonucleic acid–deoxyribonucleic acid hybridization as a second-order reaction

1973 ◽  
Vol 135 (3) ◽  
pp. 573-576 ◽  
Author(s):  
Bryan D. Young ◽  
John Paul
Keyword(s):  
Dna Hybridization ◽  
Ribonucleic Acid ◽  
Deoxyribonucleic Acid ◽  
Order Reaction ◽  
Second Order ◽  
Second Order Reaction ◽  
Reaction Theory

Certain features of RNA–DNA hybridization can be accounted for in terms of second-order-reaction theory. These include the use of annealing kinetics to estimate RNA complexity and the occurrence of approximately linear double-reciprocal plots.

scholarly journals Water defluoridation by alumina modified Turkey clinoptilolite: equilibrium, kinetic models and experimental design approaches

2017 ◽  
Vol 18 (1) ◽  
pp. 14-22 ◽  
Author(s):  
Selim Selimoglu ◽  
Esra Bilgin Simsek ◽  
Ulker Beker
Keyword(s):  
Natural Zeolite ◽  
Kinetic Studies ◽  
Order Reaction ◽  
Operating Conditions ◽  
Second Order Reaction ◽  
Freundlich Model ◽  
Box Behnken Design ◽  
Fluoride Adsorption ◽  
Exothermic Process ◽  
Pseudo Second Order

Abstract In the current work, alumina modified natural zeolite (Z-Al) was used for fluoride adsorption in aqueous solution. Effects of process parameters such as pH, temperature, initial concentration and contact time were investigated. Box–Behnken design was found effective in defining the operating conditions for fluoride sorption onto Z-Al. Confirmatory experiments were conducted to examine the reliability of the regression equation. The predicted (2.261 mg g−1) and experimental (2.289 mg g−1) capacities were found to be similar, demonstrating the accuracy of the model. The fluoride adsorption onto Z-Al was well described by the Freundlich model. Kinetic studies revealed that the adsorption followed a pseudo-second-order reaction. Thermodynamic parameters depicted that the fluoride adsorption on the alumina modified zeolite was a spontaneous and exothermic process. The co-existing ions affected the defluoridation performance significantly. Regeneration of exhausted Z-Al was achieved with H2SO4.

scholarly journals Translocation of Cations During Sorption of Copper in the System Solution - Algae (Spirogyra sp.)/Translokacja Kationów Podczas Procesu Sorpcji Miedzi W Układzie Roztwór - Glony (Spirogyra Sp.)

2014 ◽  
Vol 21 (3) ◽  
pp. 425-433
Author(s):  
Małgorzata Rajfur ◽  
Andrzej Kłos ◽  
Jan Kříž
Keyword(s):  
Order Reaction ◽  
Static System ◽  
Second Order Reaction ◽  
System Solution ◽  
Fixed Proportion ◽  
Pseudo Second Order ◽  
The Difference ◽  
Kinetics Of ◽  
Copper Cations ◽  
Solution Volume

Abstract Kinetics of the sorption of copper cations in Spirogyra sp. algae was analysed, together with the accompanying processes of hydrogen cations sorption and releasing to the solution the cations bonded in the algae: Na+, Mg2+, K+ and Ca2+. It was established that, in a static system, at the fixed proportion of algae mass to the solution volume, these processes occur simultaneously, however presumably the quantity of the released salts influences the parameters of heterophase equilibrium of ion exchange. In the experiment conditions, the quantity of the released cations was nearly 10 times larger than the quantity of the sorbed cations. The equilibrium parameters, determined from the model of pseudo second order reaction, were compared with the parameters obtained after 30 min of the process duration, ie at relatively stable indications of measuring equipment. On the example of the sorbed copper, the difference is approximately 8%. It was confirmed that the solution conductivity is a good parameter for the estimation of the state close to equilibrium.

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