钯
一氧化碳
催化作用
动力学
化学
多相催化
选择性
无机化学
光化学
有机化学
物理
量子力学
作者
Andrzej Borodziński,Geoffrey C. Bond
标识
DOI:10.1080/01614940802142102
摘要
Developments in the last three decades of kinetics of selective hydrogenation of ethyne in ethene‐rich streams on palladium catalysts are reviewed. Most of the studies can be described comprehensively by a model that assumes carbonaceous deposits (i) create irreversibly on the palladium surface small A types of active site (selective to ethene) and large E types of active site (selective to ethane), and (ii) are involved in hydrogenation of ethene on E s sites on the support. The relative importance of these sites, with varying (i) reaction conditions, (ii) palladium dispersion, (iii) process modifiers, and (iv) promoters, is discussed. Keywords: Palladium catalystsEthyne hydrogenationCarbonaceous depositsKinetic modelsMetal dispersionPromoters
科研通智能强力驱动
Strongly Powered by AbleSci AI