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CATALYTIC EXCHANGE OF METHANE AND DEUTERIUM ON PLATINUM, RUTHENIUM, AND PLATINUM-RUTHENIUM ALLOYS

Journal Article · · Journal of Physical Chemistry (U.S.)
DOI:https://doi.org/10.1021/j100785a008· OSTI ID:4068247
The exchange reaction between methane and deuterium was studied in the temperature range 70 to 200 deg C on unsupported platinum, ruthenium, and platinum- ruthenium alloy catalysts. Platinum-rich catalysts were found to be the most active and the order of initial appearance of the deuteriomethanes was CH/sub 3/D > CH/sub 2/D/sub 3/ > CHD/sub 3/ > CD/sub 4/. Ruthenium-rich alloys gave CD/sub 4/ as the most abundant initial product and the rates of formation of the different species were initially CD/sub 4/ > CH/sub 3/D > CHD/sub 3/ > CH/sub 2/D/sub 2/. In all cases, the rates of the exchange reaction were approximately first order in methane pressure and negative order in deuterium pressure. In addition, the concentration of chemisorbed hydrogen on the metal surface during the exchange reaction was followed by simultaneous measurements of the rate of formation of HD. The results indicate that the reaction takes place by different mechanisms with the two metals. With platinum, the dominant mechanism is stepwise exchange, whereas multiple exchange processes are more important in the case of ruthenium. (auth)
Research Organization:
General Electric Research Lab., Schenectady, N.Y.
Sponsoring Organization:
USDOE
NSA Number:
NSA-18-016034
OSTI ID:
4068247
Journal Information:
Journal of Physical Chemistry (U.S.), Journal Name: Journal of Physical Chemistry (U.S.) Vol. Vol: 68; ISSN JPCHA
Country of Publication:
Country unknown/Code not available
Language:
English

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