The gas-phase photochemistry and thermal decomposition of glyoxylic acid

Abstract

The photolysis of glyoxylic acid vapour has been studied at five wavelengths, 382, 366, 346, 275, and 239 nm, and pressures from about 1 to 6 Torr, at a temperature of 355 K. Major products were CO 2 and CH 2 O, initially formed in almost equal amounts, while minor products were CO and H 2 . Except at 382 nm, the system was complicated by the rapid secondary photolysis of CH 2 O. Three primary processes are suggested, each involving internal H-atom transfer followed by dissociation.The absorption spectrum is reported and shows the three distinct absorption systems. A finely-structured spectrum from about 320 to 400 nm is attributed to a transition to the first excited π* ← n + singlet state; a more diffuse absorption ranging from about 290 nm to a maximum at 239 nm is assigned to the π* ← n − state, while a much stronger absorption beginning below 230 nm is attributed to the π* ← π transition. Product ratios vary with wavelength and depend on which excited state is involved.The thermal decomposition was studied briefly in a static system at temperatures from 470 to 710 K and pressures from 0.4 to 8 Torr. Major products were again CO 2 and CH 2 O, but the latter was always less than stoichiometric. First-order rate constants for the apparently homogeneous formation of CO 2 are described by Arrhenius parameters log A (s −1 ) = 7.80 and E = 30.8 kcal/mol. Carbon monoxide and H 2 were minor products, and the CO/CO 2 ratio increased with increasing temperature and showed some surface enhancement at lower temperatures. The SF 6 -sensitized thermal decomposition of glyoxylic acid, induced by a pulsed CO 2 laser, was briefly studied, with temperatures estimated to be in the 1100–1600 K range, and the CO/CO 2 ratio increased with increasing temperature, continuing the trend observed in the static system.