The mercury (63P1) photosensitized hydrogenation of ethylene. Kinetics of the reaction C2H5 + H2 = C2H6 + H
Author(s) -
L. E. Reid,
D. J. Le Roy
Publication year - 1968
Publication title -
canadian journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.323
H-Index - 68
eISSN - 1480-3291
pISSN - 0008-4042
DOI - 10.1139/v68-541
Subject(s) - chemistry , radical , mercury (programming language) , ethylene , hydrogen , torr , reaction rate constant , analytical chemistry (journal) , chemical kinetics , kinetics , inorganic chemistry , photochemistry , organic chemistry , catalysis , thermodynamics , physics , quantum mechanics , computer science , programming language
A quantitative study has been made of the reaction of ethyl radicals with molecular hydrogen in the gas phase in the temperature range 240 to 320 °C. The mercury (6 3 Pi) photosensitized decomposition of hydrogen in the presence of ethylene was used to generate ethyl radicals. Extinction coefficients for the absorption of 2537 Å by mercury vapor were measured and Beer's law was shown to be obeyed under the experimental conditions used. The corrections required to allow for the nonuniformity of radical concentrations in the cell were small. After delineating the experimental conditions necessary to minimize secondary reactions, the rate constant (cm 3 mole −1 s −1 ) for the reaction C 2 H 5 + H 2 = C 2 H 6 + H was found to be given by log 10 k = 12.5 7 − 13.7/θ. Experiments in the presence of added carbon dioxide showed the absence of hot radical effects at the working pressure of 92 Torr of hydrogen.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom