1,3-Butadiene selective hydrogenation over Pd/alumina and CuPd/alumina catalysts

✍ Scribed by Brian K. Furlong; Joe W. Hightower; Tammy Y.-L. Chan; A. Sarkany; L. Guczi

• Book ID: 103965310
• Publisher: Elsevier Science
• Year: 1994
• Tongue: English
• Weight: 720 KB
• Volume: 117
• Category: Article
• ISSN: 0926-860X
• DOI: 10.1016/0926-860x(94)80157-6

✦ Synopsis

The selective hydrogenation of 13-butadiene was studied in the presence of a 1O:l excess of lbutene over supported bimetallic catalysts containing palladium in a vapour phase atmospheric plug flow reactor in the temperature range 288-313 K. Addition of copper to alumina-supported Pd increases its selectivity for converting butadiene to n-butenes without saturating or isomerizing the n-butenes. For example, with atomic ratio Cu/Pd=2, the bimetallic catalyst selectively converts > 99% of the diene to n-butenes while isomerizing or saturating less than 1% of the starting 1-butene. Under similar conditions, Pd alone maintains high n-butene selectivity to only about 50% conversion of the diene. Over both catalysts the kinetics of 1,3-butadiene hydrogenation are first order in hydrogen and zero order in butadiene. Hydrogen sorption experiments showed that Cu addition decreases both the surface adsorption and the bulk absorption, the former suggesting surface decoration of Pd by Cu and the latter indicating significant bulk Cu-Pd interaction in the supported bimetallic samples.