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Propane hydrogenolysis on bimetallic platinum-cobalt catalysts supported on zeolite beta synthesized with rice husk silica

机译:用稻壳二氧化硅合成的沸石β(沸石β)丙烷氢解催化剂上的双金属铂 - 钴催化剂

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Mono- and bimetallic catalysts containing Pt and Co supported on HBEA were prepared by impregnation with Pt loading fixed at 1wt% and Co loading of 5, 10 and 15wt%. The HBEA structure did not change after impregnated with metal but the HBEA crystallinity and surface area decreased with the amount of metal loading. All the catalysts were tested for propane hydrogenolysis which is a structure sensitive reaction. For monometallic catalyst, the 1%Pt/HBEA was the most active catalyst with a nearly complete conversion at 300, 350 and 400 °C but deactivated quickly. The activity and deactivation of Co/HBEA increased with metal loading. The major cause of catalyst deactivation was coking which could be removed by combustion with oxygen. Because 1%Pt/HBEA was the most active catalyst and the 5%Co/HBEA showed the least deactivation, the bimetallic 1%Pt-5%Co/HBEA was investigated further and it gave higher propane conversion and had higher tolerance to deactivation than a physically mixture between 1%Pt/HBEA and 5%Co/HBEA. Thus, a small amount of Co improved the coking tolerance of 1%Pt/HBEA catalyst.
机译:通过浸渍在1wt%和5,10和15wt%的Pt加载下,通过浸渍制备含有HBEA的Pt和Co的单催化剂和二氧化硅催化剂。浸渍有金属后,HBEA结构没有改变,但HBEA结晶度和表面积随金属负载量降低。测试所有催化剂的丙烷氢解物,其是结构敏感反应。对于单金属催化剂,1%Pt / HBEA是最活性的催化剂,在300,350和400℃下具有几乎完全转化但快速停用。 CO / HBEA的活性和失活用金属载荷增加。催化剂失活的主要原因是焦化,可以通过氧气燃烧除去。因为1%Pt / HBEA是最活性催化剂,并且5%CO / HBEA显示出最常移的,进一步研究了双金属1%Pt-5%CO / HBEA,并提供了更高的丙烷转化率,并且对失活的耐受性更高在1%Pt / HBEA和5%CO / HBEA之间的物理混合。因此,少量的CO改善了1%Pt / HBEA催化剂的焦化耐受性。

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