Kinetics of the Reaction of Atomic Hydrogen with Vinyl Chloride

1971 ◽  
Vol 49 (7) ◽  
pp. 1023-1026
Author(s):  
J. S. Tanner ◽  
J. W. S. Jamieson
Keyword(s):  
Hydrogen Chloride ◽  
Vinyl Chloride ◽  
Electric Discharge ◽  
Atomic Hydrogen ◽  
Reaction Rate ◽  
Hydrogen Atoms ◽  
Specific Reaction Rate ◽  
Flow Rates ◽  
Different Temperatures ◽  
Kinetics Of

The reaction of hydrogen atoms, produced by electric discharge, with vinyl chloride vapor has been studied at four widely different temperatures. Since the maximum yields of HCl at both 328 and 494 °C exceeded the flow rates of atomic hydrogen, the reaction was observed to have limited chain characteristics. The products were hydrogen chloride, ethylene, methane, and ethane. The specific reaction rate for HCl production was found to be about [Formula: see text] and that for production of ethylene plus ethane was found to be about [Formula: see text].

The reaction of atomic hydrogen with methyl cyanide

1970 ◽  
Vol 48 (23) ◽  
pp. 3619-3622 ◽  
Author(s):  
J. W. S. Jamieson ◽  
G. R. Brown ◽  
J. S. Tanner
Keyword(s):  
Kinetic Parameters ◽  
Electric Discharge ◽  
Hydrogen Cyanide ◽  
Atomic Hydrogen ◽  
Hydrogen Atoms ◽  
Flow Rates ◽  
Methyl Cyanide ◽  
Different Temperatures ◽  
A Minor ◽  
Minor Extent

The reaction of hydrogen atoms, produced by electric discharge, with methyl cyanide vapor has been reinvestigated at seven different temperatures between 40 and 507 °C over a range of methyl cyanide flow rates from 2 to 25 μmoles/s. As in the previous limited investigation the products have been found to be hydrogen cyanide, methane, and ethane, but the present results indicate the presence of chain characteristics to a minor extent, propagated by CN. Kinetic parameters for formation of the products have been evaluated, as kHCN = 3.55 × 10−12 e−5816/RT; [Formula: see text]; and [Formula: see text].

THE KINETICS OF THE REACTION OF ATOMIC HYDROGEN WITH METHANE

1964 ◽  
Vol 42 (7) ◽  
pp. 1638-1644 ◽  
Author(s):  
J. W. S. Jamieson ◽  
G. R. Brown
Keyword(s):  
Activation Energy ◽  
Electric Discharge ◽  
Atomic Hydrogen ◽  
Flow System ◽  
Steric Factor ◽  
Primary Reaction ◽  
Kcal Mole ◽  
Hydrogen Atoms ◽  
Fast Flow ◽  
Kinetics Of

Reinvestigation of the reaction of hydrogen atoms, produced by electric discharge, with methane in a fast flow system has given an activation energy of 7.4 ± 1.1 kcal/mole and a steric factor of about 10−3 for the primary reaction, H + CH4 → H2 + CH3.

Reaction of atomic hydrogen with tetrafluoroethene

1969 ◽  
Vol 47 (10) ◽  
pp. 1696-1698
Author(s):  
Lei Teng ◽  
W. E. Jones
Keyword(s):  
Electric Discharge ◽  
Discharge Tube ◽  
Atomic Hydrogen ◽  
Hydrogen Atoms

Hydrogen atoms, generated in a Wood's electric discharge tube, were allowed to react with tetrafluoroethene. The products of the reaction were found to be HF, C2F3H, C2H2, C2F2H2, C2F4H2, C2FH3, C2H4, and CHF3. The formation of the products with the exception of HF was studied quantitatively from 30–330 °C.

Kinetics of the Substitution of Norbornadiene in Tetracarbonyl(norbomadiene)molybdenum(0) by 2,2'-Bipyridine

2001 ◽  
Vol 56 (3) ◽  
pp. 281-286 ◽  
Author(s):  
Ceyhan Kayran ◽  
Eser Okan
Keyword(s):  
Reaction Rate ◽  
Activation Parameters ◽  
Bipy Ligand ◽  
First Order ◽  
Rate Determining Step ◽  
Vis Spectroscopy ◽  
Different Temperatures ◽  
Ft Ir ◽  
Thermal Substitution ◽  
Kinetics Of

Abstract The kinetics of the thermal substitution of norbornadiene (nbd) by 2,2'-bipyridine (2,2'-bipy) in (CO)4Mo(C7H9) was studied by quantitative FT-IR and UV-VIS spectroscopy. The reaction rate exhibits first-order dependence on the concentration of the starting complex, and the observed rate constant depends on the concentration of both leaving nbd and entering 2,2'-bipy ligand. The mechanism was found to be consistent with the previously proposed one, where the rate determining step is the cleavage of one of the two Mo-olefin bonds. The reaction was performed at four different temperatures (35 -50 °C) and the evaluation of the kinetic data gives the activation parameters which now support states.

The kinetics of the interaction of atomic hydrogen with olefines. V. Results obtained for a further series of compounds

1950 ◽  
Vol 202 (1069) ◽  
pp. 181-202 ◽  
Keyword(s):  
Double Bond ◽  
Hydrogen Atom ◽  
Atomic Hydrogen ◽  
Methyl Radicals ◽  
Hydrogen Atoms ◽  
Alkyl Radicals ◽  
Kinetics Of ◽  
Interesting Generalization

In this paper the efficiency of interaction of a hydrogen atom with a series of olefines has been determined, the olefines being members of the series obtained by progressively replacing the hydrogen atoms of ethylene by methyl radicals. The interesting generalization which emerges from this is that the efficiency of interaction does not vary very much with the nature of the alkyl substituents in the molecule, and calculations involving the heats of addition of a hydrogen atom to a double bond confirm this generalization. The data presented here are discussed critically in relation to information available on the reaction of CCl 3 radicals with olefines and of alkyl radicals with olefines, complete general agreement being demonstrated.

scholarly journals Kinetics of Thermal Degradation of Recycled Polyvinyl Chloride Resin

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
I. M. Alwaan
Keyword(s):  
Thermal Degradation ◽  
Polyvinyl Chloride ◽  
Reaction Rate ◽  
Reaction Rate Constant ◽  
Rate Of Reaction ◽  
Different Temperatures ◽  
Zero Order Reaction ◽  
Enthalpy And Entropy ◽  
Kinetics Of ◽  
Entropy Of Reaction

The goal of this study is to find the effect of time and temperature on the thermal degradation of recycled polyvinyl chloride (PVC) resin. The isothermal rate of reaction(r)of recycled PVC resin was investigated at the following temperatures to: 100, 110, 120, 130, and 140°C at period of times ranging from 10 to 50 min. The result shows that the rate of reaction(r)of recycled PVC increases with increasing temperatures. The reaction rate constant(K)for temperatures ranging from 100 to 140°C was doubled from 0.028–0.056 mol·L−1·S−1. The process was found to be zero order reaction at all range of temperatures 100–140°C. The activation energy of the thermal weight loss was calculated at different temperatures(E/R = 2739.5°K). The average enthalpy and entropy of reaction at temperature of 298°K were determined.

Kinetics of the Alkaline Solvolysis of Trichloroacetate Ion in Water-Ethanol Solutions

1978 ◽  
Vol 33 (1) ◽  
pp. 30-34
Author(s):  
I. M. Issa ◽  
E . M. Diefallah ◽  
M. R. Mahmoud ◽  
A. M. El-Nady
Keyword(s):  
Dielectric Constant ◽  
Organic Solvent ◽  
Transition State ◽  
Trichloroacetic Acid ◽  
Reaction Rate ◽  
Water Solvent ◽  
Different Temperatures ◽  
Kinetics Of ◽  
Activated Complex ◽  
Polar Water

Abstract Alkaline Solvolysis, Trichloroacetate Ion The alkaline solvolysis of trichloroacetic acid in water-ethanol mixtures have been studied in the presence of 0.40-0.80 M sodium hydroxide within the temperature range 35-70 °C. The rate constant increased with progressive addition of the organic solvent. The dielectric constant effect on the reaction rate was investigated. The radius of the activated complex at different temperatures was calculated. The isocomposition and isodielectric energies as well as the thermodynamic parameters of activation were calculated and their significance in terms of solvent composition has been discussed. It was concluded that the reactant state is extensively higher solvated than the transition state by the highly polar (water) solvent.

scholarly journals Kinetics and Mechanism of Oxidation of Isoleucine byN-Bromophthalimide in Aqueous Perchloric Acid Medium

2011 ◽  
Vol 8 (4) ◽  
pp. 1728-1733 ◽  
Author(s):  
N. M. I. Alhaji ◽  
S. Sofiya Lawrence Mary
Keyword(s):  
Acid Medium ◽  
Perchloric Acid ◽  
Reaction Rate ◽  
Activation Parameters ◽  
Halide Ions ◽  
Kinetics Of Oxidation ◽  
First Order ◽  
Hypobromous Acid ◽  
Different Temperatures ◽  
Kinetics Of

The kinetics of oxidation of isoleucine withN-bromophthalimide has been studied in perchloric acid medium potentiometrically. The reaction is of first order each in [NBP] and [amino acid] and negative fractional order in [H+]. The rate is decreased by the addition of phthalimide. A decrease in the dielectric constant of the medium increases the rate. Addition of halide ions or acrylonitrile has no effect on the kinetics. Similarly, variation of ionic strength of the medium does not affect the reaction rate. The reaction rate has been determined at different temperatures and activation parameters have been calculated. A suitable mechanism involving hypobromous acid as reactive species has been proposed.

THE REACTIONS OF 2-METHYL ETHYLENIMINE AND AZACYCLOBUTANE WITH ATOMIC HYDROGEN

1965 ◽  
Vol 43 (7) ◽  
pp. 1973-1977 ◽  
Author(s):  
J. W. S. Jamieson ◽  
G. R. Brown ◽  
W. K. Hancock
Keyword(s):  
Atomic Hydrogen ◽  
Major Product ◽  
The Other ◽  
Hydrogen Atoms ◽  
Flow Rates ◽  
Hydrogen Flow

The reactions of hydrogen atoms with 2-methyl ethylenimine and azacyclobutane have been investigated at various temperatures. Between 100 and 300 °C both reactions have been found to be rapid and complete, so that the maximum disappearance of either cyclic imine under these conditions may be regarded as a satisfactory measure of atomic hydrogen flow rates. At 300 °C ethane has been found to be a major product, and it has been inferred from this and other results at this temperature that the other major product of both reactions is cyanogen, which could not be isolated since it appears to form compounds with both cyclic imines.

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