详细信息
High Selectivity to Aromatics by a Mg and Na Co-modified Catalyst in Direct Conversion of Syngas ( SCI-EXPANDED收录)
文献类型:期刊文献
英文题名:High Selectivity to Aromatics by a Mg and Na Co-modified Catalyst in Direct Conversion of Syngas
作者:Yang, Shuo[1];Li, Minzhe[1];Nawaz, Muhammad Asif[1];Song, Guiyao[1];Xiao, Wentao[1];Wang, Zihao[1];Liu, Dianhua[1]
机构:[1]East China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
年份:2020
卷号:5
期号:20
起止页码:11701
外文期刊名:ACS OMEGA
收录:;WOS:【SCI-EXPANDED(收录号:WOS:000537629600050)】;
基金:The authors acknowledge the financial support from the National Key R&D Program of China (2017YFB0602204).
语种:英文
摘要:The demand for aromatics, especially benzene, toluene, and xylene, has been increased in recent years as the crucial feedstocks of coatings and pharmaceutical industry. In this work, a modified Fischer-Tropsch synthesis (FTS) catalyst FeNaMg was fabricated via a sol-precipitation method and integrated with an HZSM-5 aromatization catalyst for the aromatics synthesis from syngas by a one-step process. Syngas was first converted to lower olefins as intermediates on the active component of the FeNaMg catalyst followed by aromatization on zeolite. Different characterization approaches, such as BET, XRD, XPS, hydrogen temperature-programmed reduction, temperature-programmed desorption of CO, TG, and SEM, revealed that Mg efficiently optimized physicochemical properties of the Fe-based catalyst by generating a MgFe2O4 spinel structure. Further investigation demonstrated that the MgFe2O4 spinel structure could increase the syngas adsorption area, facilitating the reduction and carburization of the Fe phase, while Mg decreased CO2 selectivity (31.26 to21%) by restraining the water-gas shift reaction and improved the utilization efficiency of carbon. At the same time, alkali metal Na changed the surface electronic environment of the FTS catalyst to enhance CO adsorption as an electronic promoter, which suppressed methane formation by restraining over hydrogenation. Therefore, the synergism that existed between Mg and Na during the reaction escalated the CO conversion and aromatics selectivity to 96.19 and 51.38%, respectively.
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