摘要
测定了ZrO2负载的由不同前体得到的Ru-Fe双金属及其单金属催化剂的CO加H2反应活性。结果表明,ZrO2负载的由Ru2Fe(CO)12或RuFe2(CO)12获得的Ru-Fe双金属催化剂较负载Ru3(CO)12、Fe2(CO)9及其混合簇催化剂以及由RuCl3、Fe(NO3)3制备的常规双金属催化剂具有高得多的CO加氢活性。用程序升温分解(TPDE)方法研究了ZrO2负载的Ru3(CO)12,Fe2(CO)9及其混合簇催化剂的脱羰基过程。结果表明,除脱附作用外,负载络合物的羰基在Ar中TPDE主要歧化生成CO2,在H2中TPDE主要加氢生成CH4。
The catalytic activity for CO hydrogenation reaction of ZrO 2 supported Ru Fe bimetallic catalysts and the respective monometallic catalysts derived from various precursors was determined.It was shown that ZrO 2 supported Ru Fe bimetallic clusters obtained from Ru 2Fe(CO) 12 or RuFe 2(CO) 12 displayed much higher activity in the hydrogenation of CO than that of supported Ru 3(CO) 12 ,Fe 2(CO) 9 and their mixed metal clusters,and that of conventional catalysts prepared from RuCl 3 and Fe(NO 3) 3 The decarbonylation of ZrO 2 supported Ru 3(CO) 12 ,Fe 2(CO) 9 and their mixed cluster catalysts was investigated with temperature programmed decomposition (TPDE) method.The results indicated that besides desorption,the carbonyl of supported complexes was mainly dispropotionated to form CO 2 in Ar,whereas it was chiefly hydrogenated to form CH 4 in H 2.
出处
《石油化工》
EI
CAS
CSCD
北大核心
1996年第6期395-401,共7页
Petrochemical Technology
基金
国家自然科学基金
关键词
加氢反应
双金属催化剂
一氧化碳
钌-铁
hydrogenation of CO,temperature programmed decomposition,Ru Fe bimetallic catalysts,Ru Fe mixed catalysts,Ru 2Fe(CO) 12 ,RuFe 2(CO) 12