催化作用
醋酸
选择性
化学
乙醇
吸附
无机化学
锡
色散(光学)
铂金
钾
核化学
有机化学
光学
物理
作者
Mingchuan Zhou,Haitao Zhang,Hongfang Ma,Weiyong Ying
标识
DOI:10.1016/j.fuproc.2015.12.022
摘要
Acetic acid hydrogenation catalysts based on platinum and tin supported alumina were modified by adding potassium with different loading amounts and various impregnation sequences. The modification of K caused red shift of CO adsorbed peak, decreased Pt 4d5/2 binding energy and enhanced carbonyl group adsorption, which can promote the selectivity to ethanol. The block effect of K on acid sites was able to restrain side reaction. Further co-impregnation of Pt and Sn to K-doped support led to the poor dispersion of Pt active sites bringing about the low catalytic activity. While catalysts prepared by impregnating PtSn into K-doped alumina were not proper for acetic acid hydrogenation, but adding 0.5 wt.%K into PtSn catalyst enhanced both selectivity of ethanol from 37% to 64% and conversion of acetic acid from 88% to 93%. Further increasing potassium loading caused little change on catalytic behavior.
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