Rate Constant and Mechanism of the Reaction Cl + CFCl2H → CFCl2 + HCl over the Temperature Range 298–670 K in N2 or N2/O2 Diluent

2014 ◽  
Vol 118 (18) ◽  
pp. 3237-3242 ◽  
Author(s):  
E. W. Kaiser ◽  
Khadija M. Jawad
1963 ◽  
Vol 41 (7) ◽  
pp. 1826-1831 ◽  
Author(s):  
F. W. Evans ◽  
A. H. Sehon

The thermal decomposition of peracetic acid in toluene, benzene, and p-xylene was studied over the temperature range 75–95°C. The main products of decomposition were found to be CH4, CO2, CH3COOH; small amounts of methanol, phenols, and polymeric compounds were also detected.The rate of the overall decomposition was first order with respect to peracetic acid, and the results could be explained by postulating the participation of the two simultaneous reactions:[Formula: see text] [Formula: see text]The rate constant of reaction (1) was independent of the solvent, whereas k2 was dependent on the solvent. The ratio k2/k1 was about 10.


1972 ◽  
Vol 25 (4) ◽  
pp. 803 ◽  
Author(s):  
NL Arthur ◽  
KS Yeo

Hydrogen atom abstraction from (CH3)2S by CF3 radicals has been studied in the temperature range 79-167�: (1) CF3 + CH3SCH3 ←→ CF3H + CH3SCH2 (-1) The rate constant, based on Ayscough's value of 1013.36cmS mol-l s-l for the recombination of CF3 radicals, is given by (k1 in cm3 mol-1 s-l, E in J mol-l): Logk1 = (12.05 � 0.02)-(28710 � 130)/2.303RT Combination of these results with thermochemical data gives a calculated value of log k-1 = 12.2 - 62600/2.303RT for the rate constant of the reverse reaction. ΔH�f(CH3SCH2) and S�(CH3SCH2) are estimated to be 155.6 kJ mol-l and 290 J K-l mol-1 respectively.


1973 ◽  
Vol 26 (6) ◽  
pp. 1269 ◽  
Author(s):  
NL Arthur ◽  
BR Harman

Hydrogen atom abstraction from SiH3Cl by CF3 radicals ����������������� CF3 + SiH3Cl → CF3H+SiH2Cl������������������� (1) has been studied in the temperature range 69-168�. The rate constant, based on Ayscough's value of 1013.36 cm3 mol-1 s-1 for the recombination of CF3 radicals, is given by (k1 in cm3 mol-1 s-1, E in kJ mol-1): ������������������ logk1 = (12.38�0.06)-(25.72�0.41)/2.303RT At 400 K, the rate constant for CF3 + SiH3Cl is greater than the average value reported for CF3+SiHCl3 by a factor of 3.6. This is due to a difference in A factors since the activation energies are equal within experimental error.


1952 ◽  
Vol 25 (2) ◽  
pp. 275-286
Author(s):  
André Delalande

Abstract The addition reaction at an elevated temperature (170° C) of maleic N-methylimide with natural rubber in solution was studied. Attempts were made to apply the principles of kinetics to this thermal reaction with a view to understanding the nature of the reaction, but the complexity of the system made impossible any chance of attaining the results hoped for. A comparison of the fixation of acrylonitrile and that of maleic N-methylimide in the temperature range of 160°–200° C showed that the rates of these two reactions are in the ratio of 1 to 25–30. A determination of the unsaturation of the addition products showed that fixation is on the α-methylenic carbon atoms of the rubber hydrocarbon. Finally a mechanism of the reaction is proposed, in which free radicals play a part.


1994 ◽  
Vol 59 (5) ◽  
pp. 1086-1095
Author(s):  
Anwar Amin ◽  
Christine A. Philip ◽  
Badie S. Girgis

Ammonium metavanadate (AMV) was decomposed under pure oxygen, air, nitrogen, vacuum and controlled humidity, in the temperature range of 453 to 623 K. Three well established limiting conversions appear corresponding to the formation of ammonium tetravanadate at 453 K (50%), ammonium hexavanadate at 503 K (67%), and V2O5 at 623 K (100%). Oxidizing atmospheres have a retarding effect at 453 K but an accelerating one at 573 to 623 K, as observed from the reaction limiting time and rate constant. In addition to H2O and N2, oxygen plays an important role in the oxidation of ammonia to N2, and in the proton transfer process.


1980 ◽  
Vol 12 (8) ◽  
pp. 547-554 ◽  
Author(s):  
H. H. Lippmann ◽  
Barbara Jesser ◽  
Ulrich Schurath

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