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Designing silica-coated CoMn-based catalyst for Fischer-Tropsch synthesis to olefins with low CO2 emission
Applied Catalysis B: Environment and Energy ( IF 22.1 ) Pub Date : 2021-09-02 , DOI: 10.1016/j.apcatb.2021.120683
Tiejun Lin 1, 2 , Peigong Liu 2 , Kun Gong 1, 3 , Yunlei An 1 , Fei Yu 1 , Xinxing Wang 1 , Liangshu Zhong 1, 2 , Yuhan Sun 1, 2
Affiliation  

Co2C nanoprisms exhibit promising catalytic performance for Fischer-Tropsch synthesis to olefins (FTO) but with high CO2 selectivity (>40%). Herein, silica-coated CoMn-based catalyst was designed to limit CO2 production and remained Co2C nanoprisms as active sites unchanged. With a desired coating amount of silica, CO2 selectivity was significantly suppressed to 15.1 C% while enhancing olefins selectivity from 39.7 C% to 58.8 C%, which also shows at least 160 h of stability. It is suggested the silica-coating not only reduces the adsorption capacity of H2O, but also promotes the fast transfer of H2O away from active sites due to the higher adsorption energy of H2O on SiO2 surface, thus suppressing water-gas-shift-reaction (WGSR) activity. Moreover, the sodium promoter can counteract the H2-enrichment effect caused by SiO2-coating and largely restrain CH4 formation and olefins hydrogenation. This work provides an effective strategy to suppress CO2 formation and enhance the carbon efficiency of FTO process.



中文翻译:

设计二氧化硅包覆的 CoMn 基催化剂,用于低 CO2 排放的费托合成烯烃

Co 2 C 纳米棱柱在费-托合成烯烃(FTO)方面表现出有希望的催化性能,但具有高CO 2选择性(> 40%)。在此,二氧化硅包覆的 CoMn 基催化剂旨在限制 CO 2 的产生并保持 Co 2 C 纳米棱柱作为活性位点不变。使用所需的二氧化硅涂层量,CO 2选择性被显着抑制到 15.1 C%,同时将烯烃选择性从 39.7 C% 提高到 58.8 C%,这也显示出至少 160 小时的稳定性。建议二氧化硅涂层不仅降低了 H 2 O的吸附能力,而且促进了 H 2的快速转移由于 H 2 O 在 SiO 2表面上的较高吸附能,O 远离活性位点,从而抑制水煤气变换反应 (WGSR) 活性。此外,钠促进剂可以抵消由SiO 2涂层引起的H 2富集效应并在很大程度上抑制CH 4形成和烯烃加氢。这项工作提供了一种有效的策略来抑制 CO 2 的形成并提高 FTO 过程的碳效率。

更新日期:2021-09-10
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