J . Phys. Chem. 1992,96, 10358-10365
10358
Registry No. Cu, 7440-50-8; Cr203.1308-38-9; SO2,7631-86-9; Cr, 7440-47- 3.
References and Notes (1) Chinchen, G. C.; Denny, P. J.; Jmnings, J. R.; Spencer, M. S.; Waugh, K. C. Appl. Coral. 1988,36, 1. (2) Monnier, J. R.; Apai, G.; Hanrahan, M. J. J . Caral. 1984,88, 523. (3) Bartlev. C. J. J.; Burch. R. A d Coral. 1988. 43. 141. (4j IUier,k. Adv. carol. 1982,si;243. (5) Kung, H. H. Carol. Rev.-Sci. Eng. 1980,22,235. (6),Hefman,R. G.;Klier, K.; Simmons,G. W.; Finn, B. P.; Bulko, J. B.; Kobylmsh, T. P. J . Caral. 1979,56,407. (7) Apai, G.; Monnier, J. R.; Hanrahan, M. J. J . Chem. Soc., Chem.
Commun. 1984,212.
18) Audibert. E.: Raineau. A. Ind. Enn. Chem. 1928.. 11., 1105. (9j Eguchi, T. h e / Ecokmfsr 1936,71, 417. (IO) Sheffer, 0. R.; King, T. S. J . Caral. 1989,116, 488. (1 1) Chu, P. J.; Gerstein, B. C.; Sheffer,G . R.; King, T. S.J. Coral. 1989, 115, 194. (12) Andrew, S.P. S.Plenary Lecture (paper I2), Post Congress Symposium, 7th Internal Congress on Catalysis, Osaka, 1980. (13) Friedrich,J. B., Wainwright, M.S.;Young, D. J. J . Carol. 1983,80, 1.
(14) Chinchen G . C.; Waugh, K. C.; Whan, D. A. Appl. Coral. 1986.25, 101. (15) Chinchen, G. C.; Spencer, M. S.;Waugh, K. C.; Whan, D. A. J . Chem. Soc., Faraday Trans. 1 1987,83.2193.
(16) Takahama, T.; Oshima, H.; Ueno, A.; Kotera, Y.Appl. Coral. 1983. 5, 59. (17) Fleisch, T. H.; Mievlle, R. L. J. Carol. 1984,90, 165. (18) Friedrich,J. B.; Wainwright, M.S.;Young, D. J. J . Coral. 1983,80, 1. (19) Bartley, G.J. J.; Burch, R. Appl. Coral. 1988,43, 141. (20)Burch, R.; Chappell, R. J. Appl. Card 1988,45,131. (21) Burch, R.; Chappell, J. R.; Golunski, S.E. J . Chem. Soc., Faraday Trans. I 1989,85,3569. (22) Chen, H. W.; White, J. M.; Ekerdt, J. G . J . Coral. 1986,99,293. (23) Dell, R. M.; Stone, F. S.; Tiley, P. F. Trans. Faraday Soc. 1953,49, 195. (24) Scholten, J. J. F.; Konvalinka, J. A. Trans. Faraday Soc. 1%9,65, 2465. (25) Giamello, E.; Fubini, B.; Lauro, P.; h i , A. J . Coral. 1984,87,443. (26) Chen, M.4.; Cheng, C.-T.; Yeh, C.-T. J. Carol. 1985, 95,346. (27) Bond, G.C.; Namijo, S . N. J. Carol. 1989,118, 507. (28) Sinfelt. J. H. Chem. Eng. Sci. 1968,23, 1181. (29) Boudart, M.; McDonald, M. A. J . Phys. Chem. 1984,88, 2185. (30) Burwell, R. L.; Haller, G. L.; Taylor, K. C.; Read, J. F. Ado. C a r d 1969,20,2. (31) Dalla Betta, R. A. J . Phys. Chem. 1975,79. 2519. (32) Jalowiecki, L.; Wrobel, G.; Daage, M.; Bonnelle, J. B. J. Carol. 1987, 107,375. (33) Sheffer, G. R.; King, T. S.J. Carol. 1989,115, 376. (34) Tauster, S.J.; Fung, S.C.; Baker, R. T. K.;Horsley, J. A. Science 1981,211,1121. (35) Chaplin, R.; Chapman, P. R.; Griffith, R. H. Nature 1953,172,77.
Surface Chemlstry of Magnesium Oxide-Supported Molybdenum Oxide: An In Sltu Raman Spectroscoplc Study Si-Chung Chang,*.+ M. Anne Leugers, Analytical Sciences, Michigan Research & Development, The Dow Chemical Company, I897 Building, Midland, Michigan 48667
and Simon R. Bare* Catalysis Laboratory, Central Research & Development, The Dow Chemical Company, 1776 Building, Midland, Michigan 48674 (Received: April 2, 1992)
Supported molybdenum oxide on magnesium oxide was investigatedby in situ Raman spectroscopy as a function of molybdenum loading and calcination temperature in order to determine the molecular structures of the surface molybdenum oxide species. Molybdenum loadings from 1.0 to 26.7 wt % were studied after calcination at temperatures from 8 0 to 700 O C . For samples calcined at 600 O C in dry air the observed structure of the molybdenum oxide species was dependent upon weight loading. At low molybdenum loadings (