详细信息
Fast start-up structured CuFeMg/Al2O3 catalyst applied in microreactor for efficient hydrogen production in methanol steam reforming ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:Fast start-up structured CuFeMg/Al2O3 catalyst applied in microreactor for efficient hydrogen production in methanol steam reforming
作者:Zhang, Guiru[1];Zhao, Jiali[1];Wang, Qiang[2];Yang, Taotao[1];Zhang, Qi[1];Zhang, Li[2]
机构:[1]East China Univ Sci & Technol, Dept Chem Engn, Minist Educ, Engn Res Ctr Large Scale Reactor Engn & Technol, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Minist Educ, Dept Mech & Power Engn, Engn Ctr Efficient Green Proc Equipment & Energy, Shanghai 200237, Peoples R China
年份:2021
卷号:426
外文期刊名:CHEMICAL ENGINEERING JOURNAL
收录:;EI(收录号:20212510529456);WOS:【SCI-EXPANDED(收录号:WOS:000729433000002)】;
基金:TThis work was financially supported by the Fundamental Research Funds for the Central Universities (NO. 50321012117013), Natural Science Foundation of Shanghai (NO. 16ZR1408200) and National Natural Science Foundation of China (NO. 51776074).
语种:英文
外文关键词:Hydrogen production; Methanol steam reforming; Copper catalyst; Microreactor; DFT; Electronic interaction
摘要:The metal-oxide interaction has been proven to have extremely favorable effects on the improvement of adsorption strength tuning and catalytic performance. FeOx was found to reduce the reaction energy barrier of Cu-based catalyst in methanol steam reforming (MSR) by DFT calculation. Herein, a mesh-type CuFeMg/Al2O3 structural catalyst was synthesized and applied to MSR to explore the FeOx modification effect. In the microreactor, the catalyst showed 97.8% hydrogen yield and 2.5 times the hydrogen production efficiency of commercial catalysts. The in-situ start-up time of the catalyst without pre-reduction requires only 18 min, which is nearly 98% less time-saving compared to commercial catalysts. Meanwhile, the activity of the catalyst was basically stable in the 100-hour durability evaluation. The characterization analysis confirmed that FeOx not only enhanced the adsorption and activation capability of H2O but facilitated the rearrangement of electrons. CuFe electronic interaction had high-efficiency synergy in MSR.
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