CATALYTIC HYDRODECHLORINATION OF 1,1-DICHLOROTETRAFLUOROETHANE BY PD AL2O3/

Citation
Z. Karpinski et al., CATALYTIC HYDRODECHLORINATION OF 1,1-DICHLOROTETRAFLUOROETHANE BY PD AL2O3/, Journal of catalysis, 164(2), 1996, pp. 378-386
Citations number
26
Categorie Soggetti
Chemistry Physical
Journal title
ISSN journal
00219517
Volume
164
Issue
2
Year of publication
1996
Pages
378 - 386
Database
ISI
SICI code
0021-9517(1996)164:2<378:CHO1BP>2.0.ZU;2-W
Abstract
Palladium supported on gamma-alumina displays high activity for the hy drodechlorination of 1,1-dichloratetrafluoroethane. High H-2 partial p ressures are needed to avoid deactivation, and steady state is obtaine d after similar to 5 h time on stream. Under these conditions (H-2/CFC feed ratio = 20) the reaction is zero order in H-2 partial pressure a nd positive (0.65) order in 1,1-dichlorotetrafluoroethane partial pres sure. Three main products are formed: 1,1,1,2-tetrafluoroethane, 1-chl oro-1,2,2,2-tetrafluoroethane, and 1,1,1-trifluoroethane, with approxi mately 85% selectivity toward the desired CF3CFH2. The apparent activa tion energies associated with the formation of each product range from 52 to 68 kJ/mol. All three major products have a nonzero rate of form ation in the limit of zero conversion, the implication of which is tha t all are primary products. The kinetics results are consistent with a reaction mechanism involving a carbene intermediate. Variation of the temperature at which the catalyst is prereduced from 300 to 600 degre es C results in an increase in particle size from 11-53 nm and in an i ncrease in the hydrodechlorination TOF from 2.3 to 5.0 s(-1). (C) Acad emic Press Inc.