21) Takagi, H.; Washida, N.; Akimoto, H.; Okuda, M. Spectrosc. Lett.-1982, 15, 145-152. (22) Winer, A. M.; Graham, R. A.; Doyle, G. J.; Bekowies, P. J.; McAfee, J. M.; Pitts, J. N., Jr.CH,OH + 2 N 0 2 -CH30N0 + HN03 (1) is of much interest t o t h e atmospheric chemist in t h a t (i) i t could be a possible major source of methyl nitrite in t h e polluted atmosphere particularly when methanol is used as automobile fuel and (ii) it is an analogue to the reaction of water a n d NOz,H20 + 2NOZ -HONO + HN03T h e reaction of nitrogen dioxide and methanol, which has been known in the gas phase to proceed thermally as CH,OH + 2 N 0 2 -CH30N0 + "OB, was found t o proceed heterogeneously on various surfaces as well, in an 11-L Pyrex cell and a 6065-L evacuable smog d m n b e r . An FTIR study has revealed that t h e reaction products are t h e same as in t h e homogeneous reaction, Le,, methyl nitrite and nitric acid. Neither methvl nitrate nor nitrous acid was observed. Among the surfaces studied, uncoated were found to be the most active to induce t h e surface reaction. T h e apparent activation energy of t h e surface reaction in t h e smog chamber was determined t o be -11.9 f 3.3 k J mol-I.