催化作用
吸附
产量(工程)
化学
多相催化
无机化学
材料科学
选择性
光化学
物理化学
有机化学
冶金
作者
Thanapha Numpilai,Narong Chanlek,Yingyot Poo‐arporn,Chin Kui Cheng,Nuchanart Siri‐Nguan,Thana Sornchamni,Metta Chareonpanich,Paisan Kongkachuichay,Nevzat Yigit,Günther Rupprechter,Jumras Limtrakul,Thongthai Witoon
出处
期刊:Chemcatchem
[Wiley]
日期:2020-04-08
卷期号:12 (12): 3306-3320
被引量:88
标识
DOI:10.1002/cctc.202000347
摘要
Abstract Selective CO 2 hydrogenation to light olefins over Fe−Co/K−Al 2 O 3 catalysts was enhanced by tuning bonding strengths of adsorbed species by varying the content of the K promotor. Increasing the K/Fe atomic ratio from 0 to 0.5 increased the olefins/paraffins (O/P) ratio by 25.4 times, but then slightly raised upon ascending K/Fe to 2.5. The positive effect of K addition is attributed to the strong interaction of H adsorbed with the catalyst surface caused by the electron donor from K to Fe species. Although the Fe−Co/K−Al 2 O 3 catalyst with K/Fe=2.5 reached the highest O/P ratio of 7.6, the maximum yield of light olefins of 16.4 % was achieved by the catalyst promoted with K/Fe of 0.5. This is explained by the considerable reduction of amount of H 2 adsorbed on the catalyst surface with K/Fe=2.5.
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