Observation of an unusual surface reaction: direct abstraction of carbon monoxide from furan adsorbed on molybdenum surfaces

1991 ◽  
Vol 113 (22) ◽  
pp. 8549-8550 ◽  
Author(s):  
Glenn R. Tinseth ◽  
Philip R. Watson
Vacuum ◽  
2013 ◽  
Vol 88 ◽  
pp. 8-10 ◽  
Author(s):  
Inga V. Tvauri ◽  
Soslan A. Khubezhov ◽  
Zaurbek S. Demeev ◽  
Anatolij M. Turiev ◽  
Natalija I. Tsidaeva ◽  
...  

1989 ◽  
Vol 93 (5) ◽  
pp. 2039-2043 ◽  
Author(s):  
Yoshihiko Mori ◽  
Toshiaki Mori ◽  
Akira Miyamoto ◽  
Naoki Takahashi ◽  
Tadashi Hattori ◽  
...  

1990 ◽  
Vol 94 (11) ◽  
pp. 4575-4579 ◽  
Author(s):  
Yoshihiko. Mori ◽  
Toshiaki. Mori ◽  
Tadashi. Hattori ◽  
Yuichi. Murakami

1964 ◽  
Vol 42 (1) ◽  
pp. 1-9 ◽  
Author(s):  
Nick Demchuk ◽  
H. Gesser

The gas-phase reaction of atomic hydrogen with ketene has been investigated over a temperature range of −130° to 232 °C using a low-pressure, fast-flow system. In most cases methane, carbon monoxide, and ethane were the major products, but trace amounts of glyoxal were also detected. Above −96 °C. considerable evidence exists for the occurrence of a chain reaction carried by HCO radicals. The surface reaction at −196 °C produced methane and glyoxal predominantly with only a minor amount of carbon monoxide.


1978 ◽  
Vol 56 (1) ◽  
pp. 10-16 ◽  
Author(s):  
Bordan Walter Krupay ◽  
Robert Anderson Ross

The catalytic reaction between carbon monoxide and nitrous oxide has been studied on MnO from 493 to 573 K and on Co3O4 from 383 to 493 K. The apparent activation energy on MnO was 130 ± 4 kJ mol−1, while for Co3O4, a change from 31 ± 4 to 105 ± 4 kJ mol−1 was observed at 450 K. The rate-controlling step for the catalytic reaction on MnO was associated with the surface reaction between carbon monoxide and nitrous oxide in a manner similar to that previously reported for NiO, while for Co3O4, the rate-determining step was related to the formation of an intermediate surface carbonate. The changes in EA may be a consequence of the surface reaction proceeding via a concerted redox reaction in the low temperature region and then to a stepwise mechanism at higher temperatures resulting from the presence of structurally and energetically different forms of the intermediate surface carbonate.


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